-------
Table 3-4. TYPICAL INPUT MATERIALS FOR DRY SPINNING
6,8
Fiber
Polymer
Solvent
Acrylic
Modacrylic
Cellulose Acetate
Spandex
Vinyon
Polyacrylonitrile
Polyacrylonitrile/
Polyvinyl Chloride
Cellulose Acetate
. Polyurethane
Polyvinyl Chloride/
Polyvinyl Acetate
DM F, DM Ac
Tetramethylene Sulfone
Acetone
Acetone
DMF
Acetone,
Methyl Ethyl Ketone
3-17
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Schematic dry spinning plant
1 Spinning tank
2 Cooling water supply
3 Spinning head
4 Gear spinning pump '
5 Annular spinneret |
6 Carrier gas
7 Gas heater ',
8 Spinning shaft i
9 Shaft shell [
10 Solvent recovery '
11 Orifice [
12 Finish application rolls
13 Haul-off rolls
14 Can coiling !
Figure 3-6. Dry Spinning Cell
13-18
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discussed in detail in subsequent sections of Chapter 3. The spinning
solution is extruded through spinnerets into a precipitation bath.
Precipitation or coagulation ensues by diffusion of the solvent out of
the thread into the precipitation bath and by diffusion of the precipitant
into the thread. Between the processes employed, there is a wide variation
in the percentage composition of. the coagulation or precipitation baths
and in the temperatures applied. Wet spun filaments will undergo a
variety of additional processing steps depending on the end use.
Equipment required for wet spinning includes a solution vessel, a
metering pump, a filter, a spinneret, and a coagulant tank. Holding
tanks are employed if the products require "aging" of the polymer before
spinning. All processes include a recovery system to separate the
coagulant and solvent. Table 3-5 lists the fiber types, polymers,
solvents, and coagulants used in wet spinning. Figure 3-7 presents a
process flow diagram for a typical wet spinning process.
Filaments extruded from the spinneret are further processed in a
variety of methods depending on the end use desired. A washing step
immediately after extrusion is commonly employed to remove solvent and
other impurities. This washing step can occur either continuously or in
batches.
The important variables affecting fiber properties in wet spinning
are concentration and temperature of the polymer solution (dope) and the
composition and characteristics of the spin-bath.
Air pollutant emission points in wet spinning processes that use
organic solvents are similar to those of dry spinning, with the solvent
losses being generally less than in dry spinning. Wet spinning processes
employing solutions of acids or salts emit only small quantities of
unreacted monomer, and are therefore relatively clean from an air pollution
standpoint.-
3.1.1.5 Reaction Spinning. This process may resemble wet or dry
spinning, but always involves a continuous chemical reaction within the
fiber after extrusion which extends the polymer chain length or provides
cross-linking between chains.
This method of fiber formation is similar to that utilized in
nature (i.e., silk worms, spiders), and is basically the extrusion of a
3-19
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Table 3-5. INPUT MATERIALS FOR WET SPINNING6'8'9
Fiber
Polymer
Solvent
Coagulant
Aery!ic
Polyacry 1 on 1 tr i 1 e
Modacrylic
Rayon
Po.lyacrylonitrile-
polyvinyl chloride
copolymer
Cellulose
Dimethylacetamide
(DMAc)
Concentrated
Aqueous ZnClg
Aqueous NaSCN
Acetonitrile
DMAc
Acetone
Aqueous
Sodium Hydroxide.
Aqueous DMAc
Dilute
Aqueous
Aqueous NaSCN
Aqueous Acetonitrile
Aqueous DMAc
Water
Dilute
Sulfuric Acid
3-20
-------
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3-21
-------
pre-polymer (partially polymerized mixture), in which the chemical .
reaction (polymerization) proceeds to form the final solid polymeric
fiber after the spinning of the fiber.
Reaction spinning is not used in production of the major commodity
fibers, and its use in productibn of the specialty fibers is limited.
3.1.1.6 Post-Spinning Fiber Treatment Processes.
3.1.1.6.1 Lubrication. Surface lubrication, plasticizing, and
static protection are the three;major functions of lubrication. Sub-
sequent handling and processing; is improved when the lubricant is added
immediately after filament formation.
For melt spun and dry spun! yarns, the lubricant is applied before
winding onto a spin bobbin. Inj staple finishing it may be applied by
passing through a bath or by spjraying. The lubricant is usually added
after the washing step in the case of wet spun fibers. Most applica-
tions of the lubricant occur at- the spinning stage, by contacting the
filament immediately after spinning with the lubricant on a ceramic
wheel.
Typical antistatic lubricants are polyoxyethylene attached to
aliphatic hydrocarbon chains, Ipng-chain alky! quarternary ammonium
salts, hydroxyalkylamine salts of long chain fatty acids, high boiling
aliphatic esters, hydrocarbon o|ils, and fluid silicones. The lubricant
is applied as a solution or emulsion in water. Both the composition of
i
the lubricant and the amount applied to the fiber depend on the chemical
composition of the fiber and the end use. These lubricants are not
liberated in significant amounts in the fiber production process and do
not pose an air pollution problem.
3.1.1.6.2 Drawing. Most of the fibers undergo drawing. Drawing,
or the stretching of yarn, introduces molecular orientation to the spun
fiber and thus produces a stronger fiber. Optimum draw ratios exist for
each type of fiber. Drawing of fibers is accomplished by stretching
them between two or more rollers: one feeds the undrawn yarn and the
next roller, rotating at a greater speed, collects and feeds the drawn
yarn to another roller or to subsequent processing. The ratio of the
surface speeds of the feed and draw rollers is defined as the draw
ratio.
3-22
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3.1.1.6.3 Fiber modifications. Finally, the fibers may undergo
some fonn of physical modification to produce a specified, marketable
product. Modifications include false-twist texturing to produce inter-
filament cohesion, heat setting or heat relaxation to produce dimensional
stability, crimping to add bulk and resilience, and cutting to produce
staple products similar to natural fibers. Figure 3-8 presents a diagram
of a crimping system.
3.1.2 Production
Projected growth rates and a detailed description of economic
conditions in the synthetic fibers industry can be found in Section 9.1.
3.1.3 Location
Nearly all of the man-made fiber production facilities are located
in eight states: Virginia, West Virginia, North Carolina, South Carolina,
Georgia, Tennessee, Alabama, and Florida. Plant locations, and the type
of fiber produced can be found in the subsequent sections dealing with
each individual fiber type.
3.2 MANUFACTURING PROCESSES
The synthetic fibers manufacturing industry can generally be
characterized as having a stable commodity fiber-producing portion and a
relatively dynamic specialty fiber-producing portion, into which new
fiber types and production methods are frequently being introduced.
Still other solvent-spun fiber types are being produced at bench and
pilot-scale levels and may or nay not expand to full production '
(e.g., solvent-spun rayon). In addition, many solvent-spun fiber types
are produced in other countries that are not currently produced in the
2
U.S. Clearly, therefore, it would be inappropriate for purposes of
this study to describe each one of the almost infinite varieties of
fiber types and associated production methods employed within the fibers
industry. Rather, there are several basic solvent-spun synthetic fiber
processes that can be identified and described that adequately represent
most segments of the industry.
All fiber spinning processes share certain fundamental characteristics,
Basically, the object is to extrude a liquid or semi-solid polymer with
a desired cross section, solidify it, then collect it in a bale or wind
it on some type spool or bobbin. In most processes the solid fiber is
3-23
-------
Diagram of a stu.ffar-box crimping system
1 Rollers for introducing the tow
2 Stuff er box
3 Tempering (only with certain types)
4 Tow !
Figure 3-8. Crimping System Diagram
3-24
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subjected to further processing to enhance its mechanical properties; in
others, the fiber is taken up essentially as a finished product. Those
broadly identifiable process stages which are common to all solvent-spun
synthetic fiber processes include: (1) preparation of the spinning
solution. In this stage, polymer is dissolved in an organic solvent,
and the solution is blended with additives and filtered to complete the
preparation of the dope for spinning. (2) Spinning of the fiber, that
is, the actual formation of the fiber filaments. Polymer solution (or
dope) is forced or extruded through a device called a spinneret to
create the fiber. (3) Processing of the formed fibers. This might
include lubrication, washing, drying, heat setting, finishing, or crimping.
(4) Solvent recovery. Because of the large amount of solvent used (a
pound of polymer is typically dissolved in 2 to 3 pounds of solvent),
the economics of the industry require that almost all of the solvent
used in dissolving be recovered for reuse. Typically, solvent is recovered
most efficiently and economically at the spinning step from the spin-cells
or spin baths into which polymer solutions are extruded. .About 94 to
97 percent of the solvent used is recycled directly from the spinning
step alone. Thus, a primary solvent recovery system is an integral part
of all solvent spinning processes.
In addition to the above stages of synthetic fiber production, this
chapter will be limited to the production processes that involve the
spinning (or forming) of the fiber from a solution of polymer or pre-
polymer and organic solvent(s). There are a number of fiber types that
employ organic solvents in their production; these include acrylic,
cellulose acetate, modacrylic, polybenzimizole, spandex, triacetate,
vinyon, etc. There are basic similarities in the production sequences
for all these fiber types. Three fiber types .have been selected for
detailed process descriptions, since these types exhibit typical and
characteristic production sequences. Acrylic and modacrylic fibers
include all fibers consisting of at least 35 percent polymerized
acrylonitrile. Cellulose acetate fibers include all cellulosic fibers
with an acetylation of 15 percent or greater (includes triacetate).
Spandex fibers include all dry and reaction-spun spandex fibers in which
the fiber forming substance is a long chain synthetic polymer comprised
of at least 85 percent of a segmented polyurethane.
3-25
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3.2.1 Process Descriptions - Acrylic and Modacrylic Fiber Production
Acrylic fibers are based on the polymerization of acrylonitrile
(AN). The monomer AN is derived from propylene and ammonia. Polyacrylo-
nitrile is produced by the synthetic fibers industry with two methods:
suspension polymerization and solution polymerization. The polymers
formed are generally atactic and have an average molecular weight of
100,000 to 150,000. :
c o
3.2.1.1 Forming the Polymer.
3.2.1.1.1 Suspension polymerization. The suspension polymerization
process is accomplished by suspending small drops of acrylonitrile and
comonomers in water using violent agitation and a stabilizer which
prevents coalescence of the monomer drops. Polymerization occurs in the
presence of a catalyst that is isoluble in the monomer. Typically, the
reaction is carried out to about 65 to 85 percent completion. Insoluble
beads of polymer are formed that are subsequently filtered, washed,
refiltered, dried, milled, andjstored as powder. Monomers are recovered
from the filtration and washing steps and recycled to the polymerization
reactors. i
3.2.1.1.2 Solution polymerization. A mixture of about 96 percent
acrylonitrile and 4 percent methyl acrylate is blended with dimethylforma-
midea catalysts, and activators; it is then fed into a reactor over a
10- to 20-hour period. The polymerization temperature is maintained at
a constant level by means of circulating fluids in the vessel jacket.
Following the polymerization, the reactor effluent is passed to a
diluter for mixing with dimethylformamide containing a small percentage
of water. The diluted stream is pumped to a horizontal film evaporator
operating at reduced pressures. The residual monomer and a portion of
the dimethylformamide are stripped from the polymer stream. Pure dimethyl-
formamide is added to the polyacrylonitrile solution leaving the evaporator.
The resulting solution generally contains less than 1 percent residual
AN monomer.
The solution polymerization method offers the advantage that the
polyacrylonitrile can be used directly in the spinning process without
the need of drying and redissolving the polymer.
3-26
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Either batch or continuous reaction modes may be employed, and
either wet or dry spinning may be used to form the fibers. Polyacry-
lonitrile may be spun only from solutions and a variety of spinning
solvents are used by industry. Table 3-6 indicates the various methods
used domestically to produce acrylic and modacrylic fibers. Additional
parameters for wet and dry spinning acrylic fibers can be found in
Table 3-7. ~
3.2.1.2 Domestic Acrylic Fiber Manufacturing Processes.
3.2.1.2.1 Producer A. Polyacrylonitrile is fed to a polymer
purification system where it is washed to remove any remaining free
monomers or.catalyst residuals. The purified polymer is subsequently
dissolved in a solution of NaSCN. This results in a single phase,
3-component system of sodium thiocyanate, water, and polyacrylonitrile.
The resulting solution is blended and stored. It is then put
through a primary filtration operation to remove any suspended solids,
and is then sent to a deaeration area. Various additives are incorporated
into the mixture to give the fiber product certain desired qualities.
At the spinning stage, dope is extruded into a dilute aqueous NaSCN
solution. A washing step removes all traces of solvent from the fiber.
The water that is utilized in extrusion, prestretching., and washing'
steps is routed to a solvent recovery system after it leaves the spin
bath.
Following the washing step, the fiber bundle is drawn on rollers to
provide molecular orientation and to impart strength to the fibers, and
is then dried. A subsequent relaxing operation is employed which allows
controlled disorientation of the fiber molecules to enhance dyeability.
In the subsequent finishing and tempering stage, a lubricant and antistatic
agent is added. A crimp is added to the fibers to give them bulk. The
dried product is boxed or baled for storage and shipment.
The solvent recovery system at this company employs multiple effect
evaporators to remove the water and concentrate the NaSCN solution
exiting the washing stage. After evaporation of the water in the recovery
unit, the concentrated NaSCN solution is returned to the dissolving
step. The wastewater from the recovery system is routed to a wastewater
treatment area where it is treated and disposed of by one of two methods:
3-27
-------
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3-28
-------
Table 3-7. GENERAL PARAMETERS OF WET AND DRY SPUN ACRYLIC
FIBERS5'7
Wet Spinning
Dry Spinning
Percent polymer in dope
Pressure across dope
filters and spinning
branches
Number of spinneret holes
Haul-off speeds
Draw ratio
20-25
7-12 bars
3000-60000
5-20 m/min
1.2 to 1.6
25-35
10-15 bars
300-2000
250-500 m/min
Variable
depending on
spin gas
temperatures,
gas flow rate,
and haul-off
speeds
3-29
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(a) a deep well disposal system, or (b) a biological treatment center.
Biologically treated waters are disposed of by spray irrigation or are
discharged to surface waters.
3.2.1.2.2 Producer B. This acrylic manufacturing facility is
comprised of two separate plantsj with basically similar processing
steps. One plant produces polyacrylonitrile homopolymer. The second
plant copolymerizes acrylonitrile (AN) and other monomers to produce
products with characteristics suited to various end uses. Both plants
employ solution polymerization. Polymerization is followed by a vacuum
removal step which facilitates recovery of unreacted monomer and thereby
reduces acry.lonitrile emissions that occur during the spinning operations.
In the spinning process, po|lymer is dissolved in an aqueous solution
of zinc chloride, and is extrudecl into a coagulation bath containing a
dilute zinc chloride/water solution. The coagulated polyacrylonitrile
fibers are then washed thoroughly with water in a counter-current bath
i
to remove zinc chloride and other residuals, including monomer. A
substantial portion of the unreacted monomer returns with the wash water
to be recovered during solvent purification. Monomer loss during spinning
and washing, however, is reported to be the major source of process
Q
emissions to the atmosphere. !
Washing is followed by stretching, drying, crimping, cutting, and
baling of the fibers. Selected (products are also dyed on-line
continuously.
Unreacted monomer is carried over from the polymerization reactor;
a portion of this monomer is removed by vacuum stripping of the polymer
prior to storage. It is estimated that this vacuum flash step following
polymerization releases a majority of the unreacted AN for recovery.
The remaining monomer is released from the polymer in the spinning and
washing stages. The majority of the unreacted AN, however, is absorbed
in the dilute solvent used in the spinning and washing steps; the remaining
residual monomer is volatilized and is emitted to the atmosphere.
The major source of emissions to the atmosphere during acrylic fiber
production at this plant is volatilization of residual unreacted monomer
during the spinning and washing [operations. Testing by the company has
shown that no residual monomer remains in the fiber product. It can
3-30
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therefore be concluded that all residual monomer is released in the
spinning, washing, and drying stages. It is believed that all monomer
release occurs during spinning and washing of the fibers and that the
stretching and drying steps account for only insignificant amounts of
i 8
monomer release. .;
There are no direct or add-on emission control systems for reduction
of AN emissions applied to the plant spinning facilities. Recovery of a
portion of the unreacted AN present in the spinning solution by pro-
cessing wet-spinning and fiber washing solutions serves as an indirect
control method.
The spin bath and fiber handling equipment are partially enclosed
in order to increase the air flow rate (e.g., venturi effect) across the
polymer arid to reduce AN levels in the spinning room. Room air is
removed from above the enclosure, and the collected gases are routed to
an outlet stack. The partially enclosed spinning area also serves as a
means to maintain AN levels below the OSHA limits.
3.2.1.2.3 Producer C. Polyacrylonitrile is formed by suspension
polymerization from acrylonitrile. The polymer is filtered, and the
resulting slurry is blended and stored. The blended polymer is extruded
in the form of noodles, dried in a hot air dryer and stored. Dtmethyl-
formamide is subsequently mixed with the pulverized polymer powder and
sent to a large blending tank.
At the mixing stage pulverized polymer falls into a mixer. DMF is
sprayed onto the pulverized polymer. After being thoroughly mixed, the
resulting solution of polymer in DMF falls into a blending tank or
storage vessel where the solution is agitated. The spinning dope is
pumped through a heat exchanger which heats the polymer solution. The
heated solution is filtered through plate and frame filter presses.
These filters are hooded to reduce worker exposure to DMF during the
time when the filter media is being changed. The used filter media
(cellulose) is placed in bins and is repeatedly leached with water. The
water used for leaching is sent to the weak feed line of the DMF recovery
system.
The spinning solution is then pumped through spinnerets (containing
several hundred holes) using a metering device. The head of the spinnerets
3-31
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is kept hot by a steam jacket. Hot nitrogen gas enters at the top of
the spinning cell and moves cocurrently with the emerging filaments.
i
The DMF is volatilized or extracted by the nitrogen gas from the emerging
filaments as they travel down the length of the spinning cell. Water is
applied to the fiber at two points, and the water run-off is drained and
processed for recovery of DMF. \ A set of rolls pulls the fiber away from
the spinning cells. Fiber from multiple spinning positions converge to
form a single rope or tow which is piddled (deposited) into cans for
temporary storage. Air and solvent vapor from the can being filled is
ducted to a scrubber, while the air and vapor from filled cans awaiting
movement is .merely vented to the atmosphere. Before a filled can is
moved, a cover is placed on top of the can to reduce occupational exposure
to DMF.
The cans containing the spun fiber are transported to subsequent
washing and drawing operations. Hot water extracts residual DMF, which
is then sent to the dilute DMF (weak stream) recovery system.
Excess water is drained from the tow, and the fibers are crimped.
After crimping, the tow is piddled into a creel can. The tow is then
cut wet to form staple prior to drying, or is sent directly to a dryer
uncut. At the dryer, several tow bands are dried side by side. The
steam, solvent vapor, and hot air from the drying operation are exhausted
j
to the atmosphere. After drying, the tow is placed in cartons for
shipment or storage. !
Work areas are monitored for DMF concentration at numerous points.
Samples from these points are fed into three centralized Miran Infrared
Gas Analyzers. These points are monitored at a rate of one per minute
per analyzer.
DMF and nitrogen, vented from the spinning cell, are routed to a
condenser. . The nitrogen gas from the condenser is sent back to the top
i
of the spinning cell where it is reheated and again used in evaporating
the DMF from the extruded filaments. The condensed solvent is sent to a
"strong feed" holding tank (termed "strong feed" because this portion of
the recovery stream is very high in DMF concentration). The liquid
stream from the strong feed holding tank is next routed to the bottom of
3-32
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a large distillation column where the DMF is recovered. This distillation
column separates the solvent from water by driving off the lower boiling-
point aqueous phase.
Aqueous DMF streams from the spinning, washing, and drawing operations
are sent to a weak feed holding tank (termed weak feed because these
liquid waste streams contain low concentrations of DMF). In addition,
the gaseous exhaust (emissions) from the end or bottom of the spinning
lines is sent to a scrubber. The scrubber solution containing DMF and
water is also fed into the weak feed line. The liquid from the weak
feed holding tank is vaporized and sent to the top of the distillation
column.
Pure DMF recovered from both the strong and weak feed 'streams from
the distillation column is sent through a cooler (heat exchanger) and
solvent deionization process. It is subsequently stored in a solvent
storage tank along with any make-up solvent needed in the process. The
stored DMF is then ready for use in dissolving additional polymer.
The technology utilized by this plant represents the most effective
methods and equipment for controlling VOC emissions observed in the
industry. Emissions are captured and controlled at more points and
areas than is the average or industry-wide practice. Because of its
above-average emission control techniques, it is the only facility
considered to be operating at better than baseline control as described
in this document. Indeed, because it is not an average facility, it
forms a basis for the best technological system of continuous emission
reduction that "the Administrator of EPA determines has been adequately
demonstrated" as required in the Clean Air Act.
A new, modified, or reconstructed facility would not be required to
operate at levels demonstrated by this facility in the absence of a new
source standard; in fact, the average industry-wide practice is
characterized by less stringent capture and control. Therefore baseline
control for the dry-spun acrylic fiber model plant will be quantified
and described as the expected average practice, and not precisely existing
conditions.
3.2.1.2.4 Producer D. This company's modacrylic polymer product
is a mixture of two different polymers: a co-polymer of acrylonitrile
and vinylidene chloride and a homopolymer of N-isopropylacrylamide.
3-33
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Polymer powder is stored in silos prior to fiber production. When
needed, the polymer powder is dissolved in acetone and filtered. Filtered
dope is extruded through spinnerets downward into enclosed cabinets
20 to 30 feet long. Hot, dry air is passed through the cabinet, and
acetone solvent evaporates into! this heated stream. The solidified
fibars exiting the multiple cabinets are collected into a bundle (or
tow), then passed through a washing step. After the wash, the fiber is
crimped, dried, cut, baled, and1 stored prior to shipping.
Acetone evaporated at spinning is recovered from the spinning
cabinet air via a water scrubber system. Major acetone losses occur as
solvent evaporates from the tow as it passes through the washing, crimping,
and drying process-stages. The1 volatilized acetone from the drying
operation is sent to scrubbers for recovery. Activated carbon beds are
i
used to recover acetone from stbrage tank vents.
3.2.1.2.5 Producer E. Acrylonitrile is polymerized by the suspension
polymerization process to form polyacrylonitrile. The dry polymer (AN)
is blended with solvent (DMAc) and delusterarits in the mixing stage.
The dry polymer is fed (metered) into a mixing area to form a slurry
(partially dissolved polymer plus solvent). The slurry is pumped to
heatersj as heat is applied, the polymer is completely dissolved. The
polymer solution is fed into large holding tanks (from the bottom to
reduce air entratnment), and is then pumped to one of several filter
i
presses. Hoods over the presses collect the solvent vapor, and ducts
carry the vapor to the roof.
The dissolved and filtered polymer is then pumped through a final,
small filter and then to the sp-inneret jets. The fibers are extruded or
spun into a coagulation bath of solvent and water. The coagulation bath
is continuously drained to the [solvent recovery area. A counter-current
water wash flows across the wash area, and into the coagulation bath.
This wash water is relatively Ijow in solvent concentration as it first
flows over the moving fiber, but gains in solvent concentration as it
moves toward and into the coagulation or spin bath. The gain is due to
the continuous diffusion of solvent out of the extruded fibers. This
spin bath mixture is drained continuously and piped to the solvent
recovery area. |
3-34
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The tow bundles then proceed down the process line to the finish
area. Typically, this is a bath of lubricants and antistatic agents.
Following the finish application, the tow is passed over heated rollers.
The steam and vapor released at these points is collected by vent slots
in the spinning, washing, and drawing equipment. These vents manifold
into a large duct which leads to the roof and atmospheric discharge.
A small percentage of the fiber produced at this company is dyed on
the process line at a customer's specifications. The dyeing is performed
on selected products at the spinning/finishing/and drawing machines.
After drawing, the fiber leaves the main process line equipment and
is fed to a crimping machine. The fiber at this point is dry to the
touch. The crimping involves heating the fiber and pressing the fiber
tightly against itself, to form wrinkled or crimped fiber. A vacuum
duct is installed at the exit of the crimper to cool the fiber and
collect the vapor, which is vented to the roof. After this, a conveyor
transports and loads the tow into carts for temporary holding and movement
to subsequent processing.
The fiber is then transported to a large vessel where heat and
pressure are applied. This process is termed stress relieving. The
heated and pressurized air and vapors are vented to the atmosphere.
Next, the fiber is put through a recrimping process, since the
stress relieving removed most of the crimp induced earlier. As in the
first crimping stage, vacuum ducts are installed at the crimper box and
underneath the conveyor to cool the fiber and collect the vapors, which
are vented to the atmosphere.
A small portion of the unrecrimped continuous tow is baled for
shipment at this point. Most of the recrimped tow is carried to a
fiber-cutting operation. The cut fiber is then blown into a baling
machine. A tamper presses the loose staple into a 500 pound bale, which
is automatically weighed, bound, labeled, and covered with plastic wrap.
This type fiber plant using wet-spinning techniques is equipped
with a solvent recovery system to recover dimethylacetamide in the
solvent/water stream that came from the spinning, washing, and drawing
stages. Distillation is used to separate water from solvent in the
recovery system. The water from distillation is recycled to the spinning
operations and solvent is recycled to dope preparation.
3-35
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17-24
3.2.2 Domestic Cellulose Acetate Manufacturing Processes
There are three companies in the United States that produce acetate
fibers at five plant locations! Acetate fiber consumption is nearly
equally split between the textile fiber market and the acetate nontext ile
market, cigarette filtration tow.
Acetate is the second oldest man-made fiber and has become one of
the more important fibers in the United States. Even though more than
15 other man-made fibers have since been introduced, none has been able
to duplicate the aesthetic properties of acetate at a comparable price.
Cigarette filters made from cellulose acetate tow are widely used.
These filters provide the best balance between low price and taste when
compared with other materials.; Cigarette filtration tow is made from
the same cellulose acetate flake as textile fibers; therefore, it has
!
the same percentage of acetylation.
3.2.2.1 Cigarette Filtration Tow.
3.2.2.1.1 Producer A. Dried cellulose acetate flakes are stored
and dissolved in acetone, and a pigment is added. Dissolving occurs in
a closed, agitating mixer. The resulting batches are blended, filtered,
and sent through a metering pump which provides a constant flow of the
dope to the spinneret head.
Cellulose acetate dope is! forced through the spinneret, and the
extruded filaments are quenched with air from the scrubber. The solvent
evaporates, leaving a filament! of cellulose acetate. Acetone-laden air
exiting from the spinning cabinet (also called a quench stack) is sent
to a cold water scrubber and recycled to the quench stack. This air is
conditioned for humidity and temperature before entering the quench
stack. The cellulose acetate [filaments exit the quench stack and are
collected into a bundle or tow(. Since cigarette tow is used for filtering,
the fibers, are smaller, and the holes in the spinneret are smaller and
more numerous than those for filament or staple yarn. The post-spinning
treatment of the fiber consists of lubrication, crimping, and drying.
All solvent evaporating fjrom the extruded fiber (or filament) in
the interior of the spinning cabinet (or quench stack) is sent to a
scrubber for recovery. Emissions from the drying process are collected
and ducted to carbon beds for acetone recovery. These beds recover 92
3-36
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to 95 percent of the acetone released at the drying stage. Fugitive
emissions from other post-spinning operations are not controlled.
3.2.2.1.2 Producer B. Initially, cellulose acetate resin, which
is prepared in-house, is mixed semi-continuously with titanium dioxide
(TiOg) and acetone to make the dope. The resulting batches are blended,
then filtered in stages. The final stage is at the spinneret and serves
to protect the spinneret, rather than acting as a final filter for the
dope. Cellulose acetate dope enters the main header (manifold) and is
routed to the spinning machines, which are called metiers. Each metier
consists of a group of parallel spinning cabinets. The dope is then
metered through a pump and into the spinneret head. The extruded filaments
are quenched by room air drawn into the cabinet. The evaporation of the
solvent leaves a filament of cellulose acetate, which is collected into
a bundle or tow.
The fiber tow travels from the spinning machines to a crimper.
Each spinning line has its own crimping equipment. 'Rollers force the
tow bundle into the crimper boxes, while water is sprayed onto the
rollers. At this stage, acetone is present in the water, and there is a
measurable evolution of solvent vapors. After passing through the
crimper the tow band is sent to the dryer, which serves to dry the tow
and strip some of the finish oils. The dryers are characterized as a
2-stage system that uses low pressure steam followed by hot air. The
cigarette tow dryers exhaust directly to the solvent recovery system,
manifolding first to an air conditioning unit with cooling and heating
elements. The production process is completed at the finishing and
baling operations.
These vapor-laden air streams are manifolded into the solvent
recovery system, which leads to carbon adsorption beds. When saturated
with acetone, these beds are subjected to steam-desorption; the water-
acetone mixture is then distilled and condensed to recover the acetone.
Since a common solvent (acetone) is used in the manufacture of
acetate fiber, staple, and cigarette tow, the usual practice to manifold
all the solvent-laden air ducts into a common solvent recovery system.
The solvent recovery system generally includes one or more units of
carbon bed adsorbers with associated air coolers, fan, valves, etc.
3-37
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Each adsorption unit has three or four carbon bed adsorbers operating on
a sequential timed cycle. In normal operation, two or three of these
adsorbers would be adsorbing solvent from the solvent-laden air stream,
while the third is being desorbed with low-pressure steam. The desorbed
solvent and steam passes through a condenser, and then the acetone-water
mixture is separated by means of distillation.
3.2.2.2 Cellulose Acetate Yarn.17"24
3.2.2.2.1 Producer A. In the cellulose acetate yarn process both
continuous and batch cellulose acetate polymerization processes are
employed. The spinning process is; essentially the same as those previously
mentioned, but post-spinning treatment varies. Immediately after spinning,
the cellulose acetate filament is wound on bobbins. Some product specifi-
cations require a twist be put into the filament, after which the fiber
is wound on cores and packaged for[ shipment. The yarn may also be wound
on beams for weaving and packaged |for shipment.
All solvent evaporating from the extruded fiber (or filament) in
the interior of the spinning cabinet is sent to a scrubber for recovery.
No additional solvent recovery is practiced even though the fiber contains
up to 20 percent solvent by weight.
3.2.2.2.2 Producer B. Polymer, solvent, and other additives are
mixed in a tank by mechanical agitation. The heat of solution aids in
the dissolving of certain products. From the mixing tank the dope is
sent to successive surge or holding tanks to store the dope before being
pumped to filters. Filter presses are not hooded but use normal room
air ventilation to remove solvent [that has been released at the presses.
The filter media is periodically removed from the presses and is steamed
in ovens. This mixture of steam and solvent is sent to solvent recovery.
All waste polymer is redissolved and sent back to the primary filter
presses. The. filtered dope is sent to the spinning area.
Portions of dope are drawn from the main header and pumped to the
spinning machines (metiers).. Each metier consists of a group of side-by-
side spinning cabinets; in each cabinet dope is taken off the branch
header and passed through individual final filters. The dope is then
pumped at a controlled rate through a spinneret at the top of the cabinet.
Room air can be pulled in at the top, bottom, or center of the spinning
3-38
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cabinet depending on desired fiber characteristics. The quench air
flows cocurrently with the direction of the emerging filaments if it
enters at the top of the cabinet, countercurrently if it enters the
bottom of the cabinet, and in both directions if it enters the middle of
the cabinet.
Filaments emerging from the spinning cabinet are brought together
and taken up on a bobbin or pirn. The fiber is subsequently removed
from the bobbins or pirns and wrapped on beams or cones for shipment.
As the filament yarn fibers come out of the spinning cabinet, they
contain significant residual solvent. Room air surrounding the spinning
cabinets contains solvent which has evaporated from the yarn after it
leaves the cabinets. Each metier is equipped with a duct for exhaust of
vapor-laden air to the solvent recovery system. At sale, the residual
solvent content is down to about 1 percent. Therefore, the difference
in residual solvent content is emitted into the extrusion (spinning)
room or the twisting/beaming/coning rooms (textile area). The extrusion
room air is diluted in order to meet/maintain the'OSHA worker exposure
concentration limits on the solvents.
Improved solvent recovery could be achieved by increasing the
concentration of solvent in the room air ducted to the solvent recovery
area. However, in order to balance the desire for maximum solvent
recovery with the need for protection of workers from solvent exposure,
this company has developed a sophisticated system of in-plant air manage-
ment. This system involves the re-use of plant air from the three basic
process areas of the fiber plant. Room air from the dope preparation
area (dissolving, mixing, filtering) and room air from the twisting/coning/
beaming areas, both of which contain low levels of solvent, are vented
(transported) to the spinning room at a predetermined flow rate. The
spinning room air is then used to supply the quench air for the spinning
cell solvent evaporation. This process air, which contains a high
concentration of solvent, is vented together with a fixed amount of
spinning room air containing a low level of solvent to the solvent
recovery system. To accomplish this air management scheme properly, the
plant maintains a slight negative room pressure. The plant carefully
monitors this negative pressure as it is an important operating parameter
with regard to operation of the solvent recovery system.
3-39
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.25-28
The solvents recovered include methylene chloride, acetone,, and
methanol. A common capture and recovery system is used to collect all
the solvent-laden air from the spinning cells, together with a portion
of the air from the spinning room. The inlet solvent concentration of
i
the gases at the carbon adsorption system is relatively constant.
The carbon beds are regenerated on a time cycle basis, which is
t
adjusted through analysis of exijt stack conditions. Gas chromatographs
sequentially monitor all the carbon beds for concentrations of all three
solvents. In each recovery unit there are three carbon beds receiving
vapor-laden air while one is stemming or regenerating.
There are separate distillation columns for each solvent fraction.
The wastewater remaining after distillation contains a small amount of
solvent and is sent to the waste( treatment plant.
3.2.3 Domestic Spandex Fiber Manufacturing Processes'
Spandex is a generic name for polyurethane fiber. The Federal
Trade Commission defines spandex yarns as "a manufactured fiber in which
the fiber forming substance is a long chain synthetic polymer comprised
of at least 85 percent of a segmented polyurethane." Urethane is the
product of reacting a polyester |prepolymer with a diamine cross-linking
agent. Between the urethane groups there are long chains which may be
polyglycols, polyesters, polyamides, or copolymers of them.
Spandex is produced by two companies in the United States, each
employing a different manufacturing process. In some respects, one
process is similar to that used for acetate textile yarn, in that the
fiber is dry-spun and immediately wound onto take-up bobbins, then
twisted or processed in other ways. This spandex manufacturing process
is referred to as dry-spinning. \ The other process is substantially
different than any other fiber forming process used by domestic
synthetic fiber producers. This manufacturing process is referred to as
reaction-spinning. '
3.2.3.1 Producer A. This facility employs tetrahydrofuran as the
principal raw material; its ring is opened, and the resulting straight
chain compound is polymerized tq give a low molecular weight polymer.
This polymer is then treated with an excess of di-isocyanate. The
reactant, together with any unreacted di-isocyanate, is next reacted
with some diamine, with monoamine added as a stabilizer. The final
3-40
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polymerization stage is carried out in dimethylformamide solution, and
then the spandex is dry-spun from this solution. Thus, this manufac-
turing process is characterized by use of solution polymerization and
dry spinning with an organic solvent. Polymer (or copolymer) is dissolved
in solvent, blended with additives, filtered, dry spun, and processed.
Immediately after spinning, spandex yarn is wound onto a bobbin as
continuous filament yarn. The yarn is later transferred to large spools
for shipment or further processing in another part of the plant. As the
fibers are initially wound onto bobbins, they may still contain as much
as 5 to 10 percent residual solvent. This residual solvent continuously
evaporates into room or building air until 3 to 4 percent (by weight)
remains in the fiber.
The major emissions from the spandex dry spinning process are
volatilized solvent losses which occur at a number of points in the
overall production scheme. Solvent emissions occur during filtering of
the spin dope, spinning of the fiber, treatment of the fiber after
spinning, and during the solvent recovery process. Figure 3-9 presents
a process flow diagram, with emission points shown for this segment of
the spandex fibers industry.
Overall emissions from spandex fiber dry spinning are considerably
lower than from other dry spinning processes. It appears that the
single most influencing factor that accounts for the lower emissions is
that, because of the nature of the polymeric material and/or spinning
conditions, the amount of residual solvent in the fiber as it exits the
spin cell is considerably lower than other dry spun fibers (e.g., 5 to
10 percent versus 15 to 20 percent). This situation may be due to the
lower solvent-to-polymer ratio that is utilized in spandex dry spinning
(e.g., 1.5 to 2.0 for spandex versus 2.5 to 3.5 for acrylics and acetates),
Thus, the multi-stage condensation/distillation system which is used as
the primary solvent recovery system serving the spin cell exhaust gas,
although basically the same as in other dry spin processes, is overall
more efficient in terms of recovery of total solvent used.
3.2.3.2 Producer B. This reaction-spun spandex fiber manufacturer
forms their fiber by pumping a polyester prepolymer through multihole
3-41
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3-42
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spinnerets at a constant rate into a bath containing a dilute solution
of ethylenediarnine in toluene. The ethylene diamine reacts with
isocyanate end groups on the resin to form long-chain, cross-linked
polyester elastometric fiber. The cross-linking reaction continues for
the duration of the process. The fiber is transported from the bath via
a heated conveyor belt, through a 2-stage oven where solvent is evaporated.
The first stage of the oven is heated with steam coils, and the second
stage is heated with infrared heaters. After drying, the fiber is
lubricated and collected on tubes for shipment. Fiber sizes range from
10 to 7,000 denier.
Potential VOC emissions are from the spin bath, the heated conveyor
belt, and the drying oven. Essentially all air that enters the spinning
room is drawn into the hooding that surrounds the spin bath and conveyor
belt. This stream is ducted to a carbon adsorption (CA) system. The
first stage of the oven is also vented to the carbon adsorber. Due to
the relatively low concentration of solvent in the dryer second stage
exhaust (e.g., maximum concentration of about 30 ppm solvent), it is not
vented to the CA system. The gas streams from the spinning roan and
oven are combined and cooled in a heat-wheel type exchanger prior to
entering the bed.
The carbon is regenerated with steam, and the condensed steam and
solvent is sent to solvent recovery. There is some diamine and prepolyrner
in the aqueous phase of the condensate. After decantation of the toluene,
gentle agitation causes the remaining organics to coalese, which simplifies
separation from the aqueous phase. The toluene is then purified in a
flash distillation column.
The concentration of the inlet stream to the CA unit is maintained
at less than 25 percent LEL. The spinning room toluene concentration is
around 50 to 60 ppm. The oven exhausts are designed to maintain a
maximum concentration of 25 percent LEL.
3.2.4 Other Fibers
In addition to acrylic, modacrylic, cellulose acetate, and spandex
fibers, there are numerous organic solvent spun fibers manufactured on a
small scale, relative to the commodity fibers. Due to the wide variety
of these fiber manufacturing processes, specific products and processes
3-43
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will not be discussed. Table 3-8 lists some of these fibers along with
their producers.
3.3 BASELINE EMISSIONS
To determine the impact of possible Federal emission limitations,
it is necessary to determine the degree of control imposed by State
Implementation Plans and any other control regulations. The baseline
control used in the analysis of NSPS impacts it that level that is
typical of the industry under consideration. The impacts of an NSPS are
then calculated as incremental,impacts beyond the impact of the baseline
control.
Emission levels for fiber manufacturing facilities in the U.S. were
established using state air pollution control information, plant visits,
and information submitted to EPA in response to letters of inquiry.
These emissions are summarized in Table 3-9. The most significant
emissions from these facilities are the solvents used in the spinning of
the fiber. Solvent recovery is an integral portion of the manufacturing
processes due to the relativel^ high economic value of the solvent.
Solvent-based fiber manufacturing facilities recover between 94 and
98 percent of the total solvent they use for economic reasons, rather
than environmental or regulatory incentives. Nonetheless, the industry
i
uses such a large amount of solvent (typically 2 or 3 pounds for each
pound of fiber) that the 2 to 6 percent of solvent lost represents a
substantial tonnage of VOC emissions.
3.3.1 Acrvlic Fiber Production
VOC emissions from the acrylic fiber industry include acrylonitrile,
the polymer-forming chemical, and the various organic solvents used to
dissolve the polymer (i.e., dimethylformamide, dimethylacetamide and
acetone). Processes employing aqueous solutions of acids or salts as
polyacrylonitrile solvents have little or no solvent-related emissions
(i.e., NaSCN and ZnCl2). ; •
3.3.1.1. Wet Spun Acrylics. Major.emission points for wet spun
acrylic fibers are the filtration, spinning, washing, drying, and crimping
steps where solvent is volatilized into room air and normally vented
directly to the atmosphere. A plant of this type represents the processes
and air pollution emission control technology currently in use in the
wet spinning segment of the acrylic fibers industry. Such a production
3-44
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TABLE 3-8. TYPICAL SPECIALTY FIBERS
Fiber Trade Name
Teflon
Vyrene
Blue C Elvra
Lycra
Spandelle
Glospun
Vinyon
Polybenzinidazole
Nomex
Kevlar
Numa
Kynol
Manufacturer
DuPont
U.S. Rubber Co.
Monsanto
DuPont
DuPont
Globe Mfg. Co.
Celanese
DuPont
DuPont
Carborundum
3-45
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3-46
-------
or process sequence is considered as "baseline control." The process
lines are essentially open to room air. Ventilation hoods are located
above the spinning and washing areas and at other major processing
points.. The existing ventilation systems are designed around high air
flow rates with little emphasis on enclosures to reduce air volume flow.
There are no VOC emissions from nonorganic solvent wet spinning
processes (i.e., aqueous solutions of acids, NaSCN and salts, ZnC^)
resulting from the volatilization of solvent. Acrylonitrile emissions
from these processes would be essentially the same as the organic-based
wet spun solvent process.
3.3.1.2 Dry Spun Acrylics. Sources of emissions include filtering,
spinning, washing, drawing, steaming, and drying. Air pollution emissions
from dry spun acrylic fiber production include residual monomer (acry-
lonitrile) and solvent (dimethyl formarnide).
3.3.1.3 Dry Spun Modacrylic. The manufacturing stages are quite
similar to those of dry spin acrylic fibers. The 'major baseline emissions
from this dry spinning process are volatilized solvent losses which
occur at a number of positions in the overall production scheme. Solvent
emissions occur during dissolving of the polymer, blending of the spinning
solution (dope), filtering of the dope, spinning of the fiber, processing
of the fiber after spinning, and during the solvent recovery process.
3.3.2 Cellulose Acetate
3.3.2.1 Cellulose Acetate Cigarette Filtration Tow. The post-spinning
fiber processing steps in domestic plants are typically open to room
air; the exception is the dryer, from which emissions may be controlled.
Since the fibers as spun contain as much as 20 percent residual solvent,
significant amounts of solvent are volatilized from the fibers into the
room air. These fugitive emissions are as high as 85 kg VOC per 1,000
kg of dry .polymer produced.
3.3.2.2 Cellulose Acetate Textile Yarn. Filtration, spinning, and
post-spinning stages are the significant sources of VOC emissions in the
manufacture of cellulose acetate textile yarn. In the process sequence,
the stages including and preceding spinning are identical to those of
acetate filtration tow. Immediately after spinning, acetate textile
yarn is wound onto a bobbin as continuous filament yarn, with no further
treatment. The yarn is subsequently transferred to larger spools (beams
3-47
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or cones) for shipment or further, processing (twisting or winding, for
example) in another part of the pflant. A portion of the yarn is sold
directly in packages from the spinning machine.
As the fibers are initially wound onto bobbins, they may still
contain as much as 20 percent resjidual solvent. This residual solvent
continuously evaporates into room or building air until equilibrium is
reached at around 1 percent (by weight) residual solvent. On an industry-
v/ide basis, these fugitive emissions are about 150 kg VOC per 1,000 kg
of polymer processed.
3.3.3. Existing Regulations
3.3.3.1. State and Local Re'gulations. There are no State or local
emission regulations which apply [specifically to the production of
man-made fibers. Of the eight States that contain almost all man-made
fiber production facilities, most employ a ceiling or guideline regulating
VOC's which is similar to California's Rule 66. Two of these eight
States have little or no volatile! organic compound emission control
regulation whatsoever. These eight States are listed below with their
general VOC regulations.
Alabama: Volatile organic compound.emissions shall be limited to
40 pounds/day or 8 pounds in any 1 hour, or emissions shall be reduced
by 85 percent.
Florida: No person shall store, pump, handle, process, load,
unload, or use in any process or installation volatile organic compounds
or organic solvents without applying known and existing vapor emission
control devices or systems deemed necessary and ordered by the department.
All persons shall use reasonable |care to avoid discharging, leaking,
spilling, seeping, pouring, or dumping VOC's or organic solvents.
Georgia: There are no general regulations concerning VOC emissions
in Georgia except for certain designated industries. Synthetic fiber
manufacturing is not included in this group of industries.
North Carolina: Volatile organic compound emissions are regulated
similarly to the restrictions of Rule 66 in California (anything in
excess of 40 pounds/day must be reduced by 85 percent).
South Carolina: No applicable VOC regulations.
Tennessee: General VOC regulations state that in a county of over
100,000 people all new sources must not emit over 100 tons/year, otherwise
I
3-48
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the source would be subject to the lowest achievable emission rate
(LAER). If a county's population is less than 100,000, a source must
use reasonable and proper controls.
Virginia: The only -effective VOC regulations are those that apply
to northern Virginia. These are similar to California's Rule 66.
West Virginia: There are no effective VOC regulations, except for
control of noxious odors.
In summary, State regulatory agencies currently do not impose VOC
limitations which significantly affect man-made fiber spinning. Although
numerous control devices exist for capture and recovery of organic
solvents and other volatile organic compounds released in spinning
operations, these are operated mainly for worker protection reasons and
for economic purposes.
3.3.3.2 OSHA Regulations. Organic solvents used in the manufacture
of acrylic and cellulose acetate fibers are controlled by existing OSHA
regulations for exposure within the working area. • Acrylonitrile, the
monomer used in acrylic fiber production is also governed by these
regulations. Table 3-10 lists these VOC's and their corresponding
Threshold Limit Values (TLV) for an 8-hour day.
In order to meet these regulations most fiber producers (especially
acrylic) include additional ventilation capacity and capture systems to
reduce worker exposure. In some instances it is economically feasible
to route this additional solvent-laden gas to the solvent recovery area,
thereby increasing the percentage of solvent recycled.
Table 3-10 OSHA LIMITS FOR EXPOSURE TO SOLVENTS
AND OTHER COMPOUNDS USED IN THE MANUFACTURE
OF ACRYLIC AND CELLULOSE ACETATE FIBERS
Acetone
Dimethylacetamide (DMAc)
Dimethylforamide (DMF)
Acrylonitrile
TLV/T1/JA 8-hour day
1,000 ppm
10 ppm
10 ppm
2 ppm
3-49
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3.4 REFERENCES
1. Man-Made Fiber Producers Base Book. Textile Economics Bureau,
Incorporated. New York, New York. 1977.
i
2. Chemical Economics Handbook. Stanford Research Institute. Menlo
Park, California. March 1978. Fibers-540.000.
3. Parr, J.L. Industrial Process Profiles for Environmental Use.
U.S. Environmental Protection Agency. November 1976. Chapter 11 - The
Synthetic Fibers Industry.
4. Shreve, R.N. Chemical Process Industries. New York, New York.
McGraw-Hill Book Company. ; 1967.
I
5. Telecon. Chiti, M., Research Triangle Institute with Berard, R.,
Pacific Environmental Services, Inc. March 25, 1981. Discussion
of comprehensive list of fiber manufacturers.
6. Moncrief, R.W. Man-Made Fibers. London, Boston. Newes-Butterworths.
1975.
7. Welfers, Dr. E. Process and Machine Technology of Man-Made Fiber
Production. International Textile-Bulletin. (Schlieren/Zurich.)
World Spinning Edition: 174-204. February, 1978.
8. Click, C.N. and Moore, D.O. Emission, Process and Control Technology
Study of the ABS/SAN, Acrylic Fiber, and NBR Industries. Pull man-Kellogg,
Inc. Houston, Texas. Report to EPA, Contract No. 68-02-2619,
Task No. 6. April 1979. i
9. Report of the Initial Plant Visit to American Cyanamid Company
Santa Rosa Plant, Milton, Florida. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards for
the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. April 11, 1980.
'
10. Report of the Plant Visit to Badishe Corporation Synthetic Fibers
Plant, Williamsburg, Virginia. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development1 of New Source Performance Standards for
the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. November 28, 1979.
11. Report of the Initial Plant Visit to DuPont Corporation Waynesboro
Plant, Waynesboro, Virginia. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. May 1, 1980.
3-50
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12. Report of the Initial Plant Visit to DuPont Corporation May Plant,
Camden, South Carolina. Prepared for the Office of Air Quality
Planning and Standards5 U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. April 29, 1980.
13. Report of the Initial Plant Visit to Monsanto Company acrylic fiber
plant, Decatur, Alabama. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. April 1, 1980.
14. Economic Impact Assessment for Acrylonitrile. Enviro Control,
Incorporated. Rockville, Maryland. Occupational Safety and Health
Administration. February 1978.
15. Development Document for Effluent Guidelines Limitations and Mew
Source Performance Standards for the Synthetic Resins Segment of
the Plastics and Synthetic Materials Manufacturing Point Source
Category. Environmental Protection Agency. Washington, D.C.
March 1974.
16. Industrial Process Profiles for Environmental Use: Chapter 11.
The Synthetic Fibers Industry. EPA-600/2-77-023k. Industrial
Environmental Research Laboratory. U.S. Environmental Protection
Agency. Cinncinatti, Ohio. February 1977.
17. Reports of the Phase II Plant Visit to Celanese Fibers Company
Celriver acetate plant, Narrows, Virginia. Prepared for the Office
of Air Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards for
the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. May 28, 1980.
18. Report of Phase II Plant Visit to Celanese Fibers Company Celco
acetate plant. Rock Hill, South Carolina. Prepared for the Office
of Air Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards for
the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. August 11, 1980.
19. Report of Initial Plant Visit to Tennessee Eastman Company, Kingsport,
Tennessee. Prepared for the-Office of Air Quality Planning and
Standards, U.S. Environmental Protection Agency, during development
of New Source Performance Standards for the synthetic fibers industry.
Pacific Environmental Services, Inc. Research Triangle Park, North
Carolina. December 13, 1979.
20. Correspondence from Edwards, J.C., Tennessee Eastman Company to
Manley, R., Pacific Environmental Services, Inc. December 2, 1981.
Subject process information.
3-51
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21. Report of November 10, 1981 meeting between representatives of
Tennessee Eastman Company and EPA in Durham, N.C. Prepared for the
Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, during development of New Source Performance
Standards for the synthetic fibers industry. Pacific Environmental
Services, Inc. Research Triangle Park, North Carolina. December
21, 1981. 1
i
22. Report of September 30, 1981 plant visit to Tennessee Eastman
Company, Kingsport, Tennessee. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during developmentj of New Source Performance Standards for
the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. October 1981.
I
t
23. Report of January 2, 1982 plant visit to Tennessee Eastman Company,
Kingsport, Tennessee. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry.} Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. March 2, 1982.
24. Report of the August 11, 1980 plant visit to Celanese Fibers Company
Celco plant, Narrows, Virginia. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development! of New Source Performance Standards for
the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North.Carolina. September 1980.
25. Correspondence from Mullen1, T.W. Jr., DuPont (Waynesboro Plant) to
Manley, R., Pacific Environmental Services, Inc. June 9, 1981.
Subject spandex process information.
26. Report of the Plant Visit to Globe Manufacturing Company, Gastonia,
S.C. U.S. Environmental Protection Agency Office of Air Quality
Planning and Standards, Research Triangle Park, N.C. December 1,
1981. !
27. Correspondence from Legendre, R., Globe Manufacturing Company to
Grumpier, D.C., U.S. Environmental Protection Agency. June 26,
1980. Patent and process 'information.
28. Report of November 12, 1981 meeting between representatives of
Globe Manufacturing Company and EPA in Durham, N.C. Subject solvent
recovery and costs. Prepared for the Office of Air Quality Planning
and Standards, U.S. Environmental Protection Agency, during development
of New Source Performance Standards for the synthetic fibers industry.
Pacific Environmental Services, Inc. Research Triangle Park, North
Carolina. December 2, 198^.
29. Volatile Organic Compound Emission Inventory for Tennessee Eastman
Company. U.S. Environmentjal Agency Region IV. Atlanta, Georgia.
EPA 904/9-78-023. December 1978.
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30, Synthetic Fibers Industry, Emission Test Report Monsanto Textiles
. Company, Decatur, Alabama. U.S. Environmental Protection Agency,
OAQPS. Research Triangle Park, N.C. EMB Report 80-SNF-2.
February 1981.
31. Synthetic Fibers Industry, Emission Test Report El du Pont de Nemours
and Company May Plant, Camden, South Carolina. EMB Report 80-SNF-l.
U.S. Environmental Protection Agency. February 1981.
3-53
-------
-------
4.0 EMISSION CONTROL TECHNIQUES
4.1 INTRODUCTION
As identified in Chapter 3 of this document, volatile organic
compounds (VOC's) are the most significant air pollutants released to
the atmosphere during the manufacture of organic solvent spun fibers.
Due to the economic value of solvents used in the synthetic fibers
industry, capture and recovery of these solvents is an integral portion
of the manufacturing process. Presently, domestic synthetic fiber
manufacturing processes recover 94 to 98+ percent of the solvents used
in fiber formation. Therefore, solvent capture and recovery techniques
presently employed in the synthetic fibers industry are also indirect
methods of VOC air pollution emission control. In most cases, capture
systems with subsequent solvent recovery are applied only during the
actual spinning of the fiber; the majority of VOC emissions from the
pre-spinning (solution mixing and filtering, etc.) and post-spinning
(washing, drawing, crimping, heat setting, and drying, etc.) operations
are not recovered for reuse. Potential for additional solvent recovery
and further VOC emission control exists at these locations in the
manufacturing process.
There are five basic techniques employed in the synthetic fibers
industry to recover solvent from wet, dry, and reaction spinning
processes:
1. Gas Absorption
2. Gas Adsorption
3. Condensing
4. Distillation
5. Enclosure and Capture Systems.
These collection devices recover solvent from spinning cell solvent-laden
air during dry spinning and recover solvent from the spin bath and
4-1
-------
wash water in wet spinning. These streams contain high concentrations
of solvent and therefore possess the greatest potential for economic
and efficient solvent recovery.
i
In addition to the capture and recovery of solvent during the
actual spinning step, many wet* dry, and reaction spinning operations
incorporate hoods or complete enclosures as capture systems along
pre-spinning and post-spinning[process lines to prevent worker exposure
to solvent and unreacted monomer. Quantities of solvent released
during these portions of the manufacturing process are much smaller
than those released during theiactual spinning of the fiber, and are
usually vented to the atmosphere. Recovery of solvent at these
processing points is usually not attempted because of the relatively
i
high air flow rates necessary to reduce solvent and monomer concentrations
around the process lines to acceptable concentration levels determined
by limits on worker exposure, i
A detailed description of the solvent capture-and recovery techniques
presently employed in the synthetic fibers industry is presented
below. Because recovery process techniques may be specific to fiber
type or spinning method, a discussion of the different recovery methods
for each of the various spinning operations will be treated separately.
In addition to these methods of VOC emission control, a discussion of
other techniques available to the synthetic fibers industry to control
VOC emissions will also be presented.
4.2 GAS ABSORPTION EQUIPMENT2'3
i
Absorption equipment is designed to promote interphase diffusion
between the solute gas and the absorbent liquid. The mechanism governing
absorption techniques is believed to occur via a physical interaction
dissolving the solute gas into the absorbent, or a chemical reaction
between the two phases. Absorption requires a high degree of exposure-
surface-area to guarantee good\contact between the vapor-1aden gas and
the liquid absorbent. The efficiency of an absorber unit is dependent
upon the rate of mass transfer;which takes place betv/een the gas and
the liquid. Characteristics of the liquid absorbent such as volatility
j
and viscosity, as well as solubility properties of the solute gas in
the liquid absorbent, significantly contribute to absorber efficiency.
4-2
-------
In an effort to maximize the effectiveness of absorption techniques in
reducing or recovering process stream VOC emissions, a variety of
absorption equipment has been designed to achieve good contact between
the gas and the absorbent. These units are typically identified as
packed towers, plate or tray towers, spray chambers, and venturi
absorbers.
2 4
4.2.1 Packed Towers '
It has been shown,that systems of this type achieve high rates of
absorption. Packed tower adsorbers are vertical columns filled with
an irregularly-shaped packaging material. A liquid absorbent is
introduced .near the top of the column through liquid distributors and
is sprayed or otherwise distributed over the packing to wet the entire
surface. Absorbent liquid flows downward through the column in a
direction countercurrent to the solute gas which is introduced at the
bottom of the tower. This solid-liquid medium provides for a large
surfdce-to-volume ratio of absorbent to absorbate,-which, in turn
determines the effective contact area for the solute gas. Consequently,
the concentration of the solute gas stream decreases as it rises
through the column due to the high absorption rate of the gaseous
constituents onto the liquid absorbent, which is distributed on the
surface of the packing material. Fresher absorbent is available for
the more dilute gas stream in a zone just above any given contact
area. Figure 4-1 presents a schematic diagram of a packed tower.
When the active adsorption sites of the solid-liquid medium
become saturated with solute gas constituents, the system is defined
as having reached load point. Size and operating characteristics of a
packed tower are basically derived from, four design parameters: column
diameter, pressure drop, number of transfer units, and the height of
the transfer unit.
4.2.2 Plate or Tray Towers'
Plate or tray towers, are designed to provide contact between the
solute gas stream and liquid absorbent through a series of plates
(trays) arranged in a step-like manner. Bubble-cap plate towers are
the most common example of plate-type absorbers. Typically the plates
permit deposition of the gas onto the liquid surface through plate
.2,4
4-3
-------
t GAS OUT
LIQUID-
If
LIQUID DISTRIBUTOR
PACKING
RESTRAINER
SHELL
RANDOM
PACKING
LIQUID
RE-DISTRIBUTOR
PACKING SUPPORT
GAS IN
LIQUID OUT
Figure 4-1. Schematic ;Diagram of a Packed Tower"
4-4
-------
openings covered with caps. Vapor rises through the plate apertures
and exits the caps via peripheral slots which direct the gas onto that
portion of the plate which is immersed in liquid. Liquid travels
through the column in a cascade fashion by entering the top of the
tower, flowing across each plate, and down through each series of
plates by way of downspouts. Design parameters for plate or tray
towers include: gas velocity, temperature, liquid flow patterns, plate
spacing, and depth of liquid on the plate. The number of stages
necessary to theoretically remove a given percent of the solute gas
from the gas stream is divided by the actual number of plates required
for the same system in order to determine the overall efficiency of
the tower. Figure 4-2 illustrates the design of bubble-cap tray
towers.
4.2.3 Spray Chambers2'4
A more simplistic approach to accomplishing interphase contact
between the solute gas and the liquid absorbent is'exemplified by
spray chamber absorbing units. Typically, this device consists of an
empty chamber equipped with a series of nozzles which spray a liquid
over the cross section of the vessel as the gas passes through the
spray. The size of the spray droplets affects the efficiency of this
type absorber by determining available surface area for contact between
the two phases. Spray nozzles can be selected to provide droplet
sizes ranging from 500 to 1,000 microns. Solubility characteristics
of the solute gas-absorbent mix will also contribute to percent removal
or recovery values for process stream pollutants.
4.2.4 Venturi Absorbers2'4
Venturi absorbers, like spray chambers, can be. used to reduce
gaseous emissions. The venturi type absorber accomplishes interphase
contact between the solute gas and the liquid absorbent by introducing
the gas and the liquid into the throat of the venturi at different
velocities. High gas velocities required by the venturi serve to
increase the effective collision between the gas and liquid streams.
Power requirements necessary to provide such high velocities can be
large, due to the fact that energy is dissipated in the form of a
4-5
-------
I I f GAS OUT
SHELL— •
TRAY
DOWNSPOUT -
TRAY
SUPPORT RING -
TRAY
STIFFENER-
VAPOR
RISER
FROTH—-
,^y-p:-^
^-LIQUID IN
BUBBLE CAP
SIDESTREAM
'WITHDRAWAL
.INTERMEDIATE
FEED
— GAS IN
~ LIOUID OUT
Figure 4-2. Schematic Diagram of a Bubble-Cap Tray Tower"
4-6
-------
pressure loss. Venturis have the advantage of obtaining a high degree
of liquid-gas mixing, but have the disadvantage of short contact
times. High velocity requirements can also generate an entrainment
problem, which usually necessitates the use of a mist eliminator
downstream in the system.
4.2.5 Gas Absorption Equipment as Currently Employed by the Synthetic
_j^
Fibers Industry
4.2.5.1 Dry Spun Acrylic Fibers.1'12 Dry spinning of acrylics
is performed by extruding a solution of polymer in an organic solvent
(usually dimethylformamide) through a spinneret plate into a spinning
cell. A column of hot inert gas that is above the boiling point of
the solvent is circulated in the direction of the emerging spinning
solution. The solvent evaporates into the spinning cell leaving a
solidified filament. The solvent-laden gas stream is routed to a wet
scrubber. Approximately 90 percent of the total solvent introduced
into the system is recovered at the spinning cell.- Capture and recovery
of solvent from the spinning cell quench gas serves as an indirect
means of controlling VOC emissions.
• At the exit of the spinning column the fiber contains from 15 to
30 percent solvent by weight. Most of this residual solvent is removed
from the spun fiber in the subsequent washing, drawing, crimping, and
drying process stages. Some residual solvent remains in the final
product. Partial enclosures are used around pre- or post-spinning
stages to capture volatilized solvent so that OSHA standards for
occupational exposure in the work area can be met. These enclosures
are vented to the atmosphere; no attempt is made to recover or control
these emissions via conventional air pollution control equipment.
1 12
4.2.5.2 Dry Spun Cellulose Acetate. * Recovery of solvent
from the spinning of cellulose acetate fibers is accomplished in the
same manner as solvent recovery from dry spinning of acrylic fiber.
Air entering at the top of the spinning cabinet flows cocurrently with
the direction of the extruded filaments and removes volatilized solvent
(acetone) from the acetate filaments. The air stream or quench gas,
containing high concentrations of acetone, exits the spin cell and is
sent to a solvent recovery device. When wet scrubbing is used as the
4-7
-------
4
recovery device, the acetone in solution with water is transported to
a distillation column where the acetone is separated for recovery and
reuse. [
As the fiber exits the spin cell it contains as much as 20 percent
acetone by weight. The remaining post-spinning processes are usually
uncontrolled, and residual acetone in the fiber is allowed to evaporate
I
into the room air. Because the TLV for acetone is relatively high,
and stringent precautions are not necessary to minimize worker exposure,
little or no attempt is made to capture and remove fugitive acetone
emissions along the other portions of the process line. Instead,
general room air ventilation is used to maintain the solvent concentration
at acceptable levels. Emissions from the filtering of the dope prior
13
to spinning are also uncontrolled.
4.2.6 Gas Absorption Equipment Performance
VOC control efficiencies of scrubbers are known to exceed 99 percent.
Absorption is highly dependent I upon solubility for" effectiveness.
High solubilities tend to reduce the column's liquid-gas ratio by
minimizing the required liquid flow rate for a given efficiency.
Concentration of the exhaust stream influences the selection of absorber
design. If very low concentrations of a highly soluble VOC are directed
to the absorber, the size of the tower can be relatively small and
gas-liquid throughputs can be optimized. In the case of highly concentrated
streams of a fairly insoluble material, long residence times and/or
larger towers are necessary to promote contact. Acetone, DMF and DMAc
are infinitely soluble in water, thus a favorable equilibrium can be
established that will promote effective VOC removal efficiencies.
The total emission rate of the vapor-laden gas stream, more than
any single parameter, governs the size of the absorber unit. Temperature
is also an important variable to be considered in the design of an
absorber. The gas volume affects the size of the collector regardless
of the method of absorption chosen. The exhaust gas flow rates and
concentrations of the solvents at synthetic fiber plants make VOC
scrubbing using water as the absorbent a practical control technique.
Packaged towers, plate towers, and spray chambers are the types
of absorption devices most effective for VOC collection. However,
4-8
-------
there are advantages and disadvantages for each system, and final
2
selection should be based on the following comparative information:
• if the gases tend to be corrosive, as are DMF and DMAc, packed
towers are generally less expensive than plate towers;
• if throughput is the same, packed towers will exhibit smaller
pressure drops than plate towers;
• liquid "hold-up" is usually less in a packed tower;
• packed towers tend to plug more readily than do plate towers;
• plate towers are better suited for continuous temperature
variations;
• spray chambers demonstrate a lower absorption efficiency than
both packed and plate towers.
4.3 GAS ADSORPTION EQUIPMENT15"17
Gas adsorption equipment (primarily carbon beds) has been used
for solvent recovery by the synthetic fibers industry and other indus-
tries for many years. In general terms, the principle behind adsorption
as it applies to the synthetic fibers industry may be described as
follows: the "activated" carbon constitutes the adsorbent, and the
organic solvent that is removed from a gaseous stream is referred to
as the adsorbate. Adsorption occurs at the gas-solid interface of the
adsorbent. The mechanism of adsorption is believed to be a combined
effect of: physical adsorption of the adsorbates without a chemical
change; Van der Waals forces between the carbon surface and the gas
that acts to form layers of gas molecules; and capillary action that
occurs in the fine pores of the absorbent material. Adsorption is an
exothermic process, and cooling may be necessary to prevent excessive
heat buildup.
There are several variables which affect the performance of
carbon adsorbers, and most are related mathematically to the adsorptive
capacity of the carbon. Adsorptive capacity defines the weights of
adsorbate that can be retained on a given weight of carbon, and is
1 ft
expressed below:
Adsorptive Capacity =
Vm
log {Co/c1)
4-9
-------
where, adsorptive capacity , gs g adsorbent
Vm = liquid molar volume of adsorbate at normal boiling point
T = absolute temperature
Co = concentration of adsorbate at saturation
Ci = initial adsorbate concentration into adsorber.
The liquid molar volume of a|n individual adsorbate is related to the
individual molecular weight and density of the solvent at its boiling
point. The greater the Vm of the adsorbate, the higher the molecular
weight and boiling point. iji other words, carbon generally has a
greater adsorptive capacity for higher boiling point and higher molecular
weight solvents. The remova^l of solvents by physical adsorption is
practical for adsorbates with molecular weights over 45.
19
Adsorption equipment is designed to collect and retain vapors on
the adsorbent material until, the absorbent becomes saturated. Adsorber
units can allow for either regeneration (desorption) or disposal of
the used adsorbent material.; Nonregenerative systems are units that
do not reuse spent absorbent and require that the adsorbent material
be removed for regeneration or incineration.
The adsorption cycle takes place in two stages: adsorption and
regeneration. Initially, the adsorption rate of gaseous vapors is
rapid and complete; but as the adsorbent is saturated, collection
efficiency of the system decreases. Regeneration requires that a hot
gas, usually steam, be passed upward through the bed, which drives off
i
adsorbed compounds. Following regeneration but prior to the control
system being put on-stream, cooling and drying of the bed is necessary
due to the temperature and water content of the adsorbent. Insufficient
cowling and drying will result in reduced efficiency. If the desorption
feature is an integrated component of the solvent recovery system,
then the vapor-laden effluent is condensed and separated by decantation
or distillation. Figure 4-3; shows a typical carbon adsorption process
employed in the synthetic fibers industry.
Adsorbers can have fixed, moving, or fluidized beds, and can be
opened either vertically or horizontally. The simplest adsorber
design is a vertical cylindef containing a fixed bed adsorbent sandwiched
4-10
-------
•=£ OL _J D-
0 0 _, _
to
t/1
ID
O
O
D-
O
to
-a
(O
O
O)
o
a-
=1 >
4-n
-------
between screens. Typically, tfixed bed adsorbers are a two-unit system;
one adsorber cleanses the vapor-laden stream, while the second bed
undergoes regeneration. Three-bed adsorber units usually employ one
bed for adsorbtion, a second bed for regeneration, while the third bed
undergoes cooling and drying.; Figure 4-4 illustrates three different
configurations for carbon adsorption that could be employed in the
synthetic fibers industry. Fixed bed adsorbers may be designed in a
cone shape. This type of construction allows for a large adsorbent
surface area exposure. Higher gas flow rates at lower pressure drops
are accommodated by cone-shaped units in contrast to a flat bed system
using the same total weight of adsorbent. Horizontal beds are also
employed, with the carbon beds enclosed in a cylinder.
A moving bed configuration passes activated carbon through an
adsorption zone. Due to fresh adsorbent continually being fed into
the adsorbing zone, moving bed adsorbers demonstrate higher collection
efficiencies than stationary bed systems. Disadvantages include wear
on moving parts, more rapid attrition of adsorbent, and higher steam
! 17
requirements for desorption due to shorter carbon beds.
4.3.1 Applicability to The Synthetic Fibers Industry
4.3.1.1 Dry Spun Cellulose Acetate and Triacetate.'
Three fiber producers are currently employing carbon adsorption as a
means of recovering solvents from their cellulose acetate production
lines. In one case, volatilized solvent (acetone) from the drying
process is sent to carbon beds for acetone recovery. Steam is used to
strip the solvent from the carbon beds, then the condensed steam and
acetone is distilled. Approximately 92 to 95 percent of the acetone
i
released at the drying stage is recovered by the carbon adsorber.
In another case, acetone-laden air from the spinning cells discharges
into several carbon beds. Again, steam is used to strip the acetone
from the carbon beds. Once stripped, the acetone-laden stream is
condensed, cooled, and pumped to stills where the acetone is separated
from the solution and recovered for reuse. It is reported that this
i
system routinely achieves 98 [percent efficiency after capture of the
vapor.
6-11
4-12
-------
VAPOR-LADEN
AIR IN
CARBON
CYLINDRICAL
SHELL HOUSING
VAPOR-FREE
AIR OUT
VAPOR-FREE
AIR OUT
FRESH CARBON
DISPENSER
SPENT CARBON
COLLECTOR
VAPOR-LADEN
AIR IN
VAPOR-LADEN
AIR IN
VAPOR-FREE
AIR OUT
Figure 4-4. Carbon Adsorption Methods
4-13
-------
The third producer employing carbon adsorption as a means of
solvent recovery from their cellulose acetate production lines uses a
common adsorption system which serves both filament and tow product
lines. The two solvent recovery processes associated with filament
extrusion operations and tow extrusion operations are housed in separate
facilities. Two vapor-air ducjts and a room-air duct connect the two
facilities. The solvent recovery system is common to both operations
inasmuch as all absorbers are interconnected via the room air and
vapor ducts.
Some of the room air is mpved directly via the room air duct from
the filament extrusion building to the tow extrusion building. Heated
room air is drawn into the filament spinning machines as quench air.
Concentrated solvent vapor-laden air from the spinning machines is
ducted to adsorption units. The recovery process differs in the
production of the two types of fiber, textile filament and tow only in
that the vapor-laden air is cooled before ndsorptton in the filament
recovery system by means of a wet (spray) cooler; while in the tow
recovery system, the vapor laden air is cooled using dry coil heat
exchangers. As with the other adsorber systems mentioned previously,
steam is introduced into the bottom of the carbon beds to desorb
i
acetone. Condensers and distillation stills are used to recover
98 percent of the collected acetone for reuse in fiber production.
This same fiber producer also employs carbon adsorption at another
filament yarn facility. However, a different solvent recovery strategy
is used. This system involves the reuse of plant air from the three
basic process areas of the fiber plant. Room air from the dope preparation
area (dissolving, mixing, filtering) and room air from the twisting/
coning/beaming area, both of which contain low levels of solvent, are
i
vented to .the extrusion room at a predetermined flow rate. The extrusion
room air is then drawn into the spin cell to supply the quench air for
solvent evaporation. Quench air containing a high concentration of
solvent is vented together witjh a fixed amount of extrusion room air
(which contains a low level of solvent) to the carbon adsorption
system. The solvents recovered at this facility include methylene
chloride, acetone, and methanol. Again, steam is used to desorb the
4-14
-------
solvents. A separate distillation column is used for each solvent
fraction. Solvent recovery at this facility is approximately 95 percent.
20
4.3.1.2 Wet-Spun Spandex Fibers (Reaction Spun Spandex). As
identified in Chapter 3 of this document, wet spinning of spandex
fibers or reaction spinning is performed by extruding a polyester
prepolymer through spinnerets at a constant rate into a solution of
(usually) ethylenediamine in toluene. A chemical reaction precipitates
the polymer, which is withdrawn from the bath and placed on a moving,
heated conveyor belt. The chemical cross-linking reaction continues
for the duration of the process. From the heated conveyor the fiber
is drawn through an oven, then wound on packages.
Air pollutant emissions from the reaction-spun spandex process
line originate at the spin bath, the heated conveyor belt, and from
the oven. Essentially, all air that enters the spinning room is drawn
into the hooding that surrounds the spin bath and conveyor belt. This
stream is ducted to a carbon adsorption system. The first stage of
the oven is also vented to the carbon adsorber.
The carbon is regenerated with steam. Condensed steam and solvent
is sent to the solvent recovery area. There is some diamine and
prepolymer in the aqueous phase of the condensate. After decantation
of the toluene, gentle agitation causes the remaining organics to
globulate, which makes them easy to separate from the aqueous phase.
The toluene is purified in a flash distillation column.
Overall solvent recovery associated with the reaction-spun spandex
process is currently not as efficient and economical as in other fiber
production processes. Over 99 percent of the organic vapors evolved
in the reaction-spun process are captured and sent to solvent recovery.
However, a rather complex fouling phenomenon in the carbon bed decreases
the solvent recovery efficiency to less than 90 percent rather quickly.
Apparently, unreacted prepolymer and diamine cause such severe carbon
bed fouling within the adsorption system that the carbon pellets are
cemented into a hardened asphalt-like solid. The consequential removing,
shipping, and reactivation of the carbon is a large expense to the
producer. It appears from an investigation into the carbon fouling
problem that there is no short-term solution to the lower solvent
recovery efficiency associated with the reaction-spun spandex process.
4-15
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4.3.2 Gas Adsorption Equipment Performance
Custom packaged carbon adsorption designs feature flow rate
accommodations of less than TOO scfm to 80,000 scfm. Review of exhaust
flow rate data from the synthetic fibers industry, show that flow
rates from uncontrolled emission sources range from 5,000 acfm to
60,000 acfm. On the average:, VOC exhaust gas characteristics are
reported to range from 100 ppm to 3,000 ppm, falling well within
design specifications. As identified in the previous section, carbon
adsorption efficiencies rangp from 92 to 98 percent. Several factors
are attributable to this range of collection efficiencies. Recent
industry efforts to recover residual acetone have included the treatment
of all dryer exhaust gas for solvent recovery. As a result of high
moisture content in the gas ;stream and the presence of finish oils
which contaminate the carbon beds, the adsorption efficiencies achieved
on treatment of this gas stream are somewhat lower than other carbon
21 22
adsorption applications. ' Therefore, based on- industry operating
experience, a recovery efficiency of about 92 percent is normally
expected for carbon adsorption systems servicing streams with high
moisture content.
It appears that solventrladen air streams containing two or more
VOC's, such as that encountered at the facility that produces cellulose
triacetate textile filament |yarn, may result in several adverse effects
upon the carbon adsorption system. Adsorption of organic compounds
having higher molecular weights will tend to displace those having
lower molecular weights. Lighter compounds will tend to be separated
or partitioned from the heavier and will pass through the bed at a
faster rate. This will increase the mass transfer zone, and may
require additional carbon bed depth, or shorter operating cycles.
i
Also, carbon retentivity may be reduced in accord with the above, and
i
breakthrough conditions may result for lower-boiling materials. The
LEL of the mixture will also vary directly as the LEL of the individual
components. Thus, safety considerations might require more or possibly
i
less dilution air with multiple organic feeds. Due to the adverse
I
effects associated with solvent-laden air streams containing two or
more VOC's, the carbon adsorption efficiency of any given system will
4-16
-------
tend to be lower with a multiple organic feed than with a single
23
organic feed. Therefore, the typical efficiency for a system handling
a multiple organic feed is expected to be approximately 95 percent.
1 IQ ?4 ?£,
4.4 CONDENSATION i»iy»^»«
Recovery of condensible vapors is accomplished by passing vapor-air
or vapor-inert gas mixtures over relatively cold surfaces, resulting
in direct condensation of the vapors. The principle of condensation
of solvent vapors is the operation of the condenser at increased
pressure or reduced temperature to change the solvent from its vapor
to the liquid phase, simplifying recovery or further processing.
The two types of condensers that can be employed are contact and
surface condensers. Contact condensers require that the coolant
physically mix with the vapor-laden gas stream, and this method is the
more efficient of the two. . However, in contact condensation, the
condensate is contaminated with the coolant liquid, and further treat-
ment is necessary for condensate recovery. For this reason, the
surface-type condensers are usually utilized in cases where the condensate
will be recovered for reuse, rather than being incinerated or sent to
waste treatment.
Most surface condensers are the shell and tube type. The coolant
flows through the tubes, and the vapor condenses on the shell side.
The amount of cooling required depends on the inlet vapor concentration
and flow rate and the design concentration of the exit gas. Also, the
presence of any contaminating substances that might be deposited on
the cooled surfaces might inhibit heat transfer and reduce condensation
efficiency. Also, the inlet vapor temperature is important, since the
entire stream must be cooled to the condensation temperature of the
compound being removed from the stream.
4.4.1 Applicability to the Synthetic Fibers IndustryJ
Condensers are used throughout the synthetic fibers industry, and
are used both independently for solvent recovery or as part of a
larger recovery system that may include scrubbers or carbon beds. In
those cases where condensers are used independently, the solvent is
usually recovered from a closed loop. Spin cell gas (such as heated
nitrogen) that contains a high concentration of solvent vapor is
16-21
4-17
-------
ducted to the condenser, where the solvent is recovered economically
(due to the high concentration) for immediate reuse or storage. When
used alone for vapor control, refrigeration is the usual means of
achieving the low temperatures necessary for efficient condensation.
Temperatures as low as -120°(r are normal. In other cases, condensers
may collect the steam and concentrated vapor from carbon beds (during
the regeneration cycle), to be followed by distillation or decantation
to separate the solvent from1 the condensed mixture.
4.4.2 Performance Characteristics
The operation efficiencies and costs for condensers depend on the
following:,
• the concentration and nature of the vapors in the gas stream
• the average temperature difference between the inlet gas and
the coolant !
• the nature of the coolant or refrigerant
• the presence of noncbndensible gases in the inlet gas stream
• the presence of particulates or other contaminants (oils,
etc.) in the inlet stream
• utility costs
• recovery credit for reclaimed solvents
In the closed loop operation, where contamination is low and
vapor concentration is relatively high, recovery efficiencies are
dependent on several variables, but are reported greater than 96 percent
for some saturated hydrocarbons. In uses where ambient air is mixed
with the vapor and some contamination is present, usual efficiencies
of about 90 percent are reported. Advantages and disadvantages of
i I
condensation as a control technique are given in Table 4-1. <
4.5 DISTILLATION
p£
4.5.1 General Description
Distillation is the separation of compounds usually in the liquid
phase by partial vaporization of the mixture and separate recovery of
the vapor and residual liquid. The lower the boiling point of a
constituent, the greater its proportion in the vapor phase, and the
lower its concentration in the residual mixture. The degree of separation
of the various compounds introduced depends on the properties of the
compounds and the characteristics of the distillation process. Usually,
4-18
-------
Table 4-1. ADVANTAGES AND DISADVANTAGES OF EMPLOYING
22
CONDENSATION AS A CONTROL TECHNIQUE
ADVANTAGES
1. Proven technology in other nonrelated industries.
2. Recovered heterogeneous mixtures of organic solvents
could be burned in a process boiler.
3. Heat exchangers and low temperature cooling coils can
reduce cooling requirements (sometimes up to 75 percent).
4. May perform best as an integral part of other air pollution
control equipment.
DISADVANTAGES
1. At a solvent concentration in the 100 to 200 ppm range,
refrigeration costs would be very expensive.
2. Large air volumes or particulate matter can reduce
condensation efficiencies by as much as 50 percent.
3. Cooling requirements are more demanding for heated exhaust
streams, such as from dryers.
4-19
-------
distillation refers to the vaporization process in which the vapor
evolved is recovered, usually;by cooling or condensation.
In batch distillation, the mass of material to be distilled is
heated to the boiling point oV the material to be recovered in a
i
container, and the vapors pass upward through a column, then to a
condenser. This process continues until the distillate concentration
in the residual material is reduced to an acceptably low level.
In continuous distillation, a feed stream is partly vaporized
while the vapor and liquid portions are continuously withdrawn.
Startup of such a unit is the same as in batch distillations except
that no product is removed via the overhead column. When steady state
conditions are achieved, the feed is continuously added at some inter-
mediate point in the column, j The portion of the column above the feed
point is the enrichment section, and the section below the feed point
is known as the stripping section. Vapor is continuously withdrawn
and condensed. This type distillation is used in -conjunction with
steam distillation in some applications.
Steam distillation is the vaporization of the feed by blowing
live steam through it, and fe|ed of the steam/vapor/volatiles mixture
into the separation column. This is especially useful when excessive
temperatures should be avoided.
16-21
4.5.2 Applicability to the Synthetic Fibers Industry
Synthetic fiber producers use distillation extensively in solvent
recovery systems. Separation and purification of the solvent used in
preparation of the spinning solution is a critical step in fiber
manufacture. Manufacture of ;all but the most exotic and expensive
fibers requires recovery and reuse of the solvent for economic reasons.
The solvent fed to distillation is usually mixed with water, or
is even a .mixture of several solvents, each with a particular function
in the overall process. A peculiar phenomenon occurs when several
solvents are used and recovered that should be mentioned. While
separation and recovery efficiencies of 98 percent and greater are
common for distillation of a single solvent from a water/solvent
mixture, lower efficiencies are observed in multi-solvent systems.
This apparently results from the characteristics of the various
4-20
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azeotropes formed, and more of each solvent is removed from the system
than would otherwise occur. (It may also be possible that lower
efficiencies result from varying carbon adsorption efficiencies among
the constituents, and other phenomena such as preferential breakthrough.)
In dry spinning, the solvent is removed from the vapor stream by
use of carbon adsorbers or scrubbers, and the solvent/water mixture is
then separated by distillation. In wet spinning, a solution of polymer
12
in solvent is extruded through a spinneret into a spinning bath.
The spinning bath contains solvent diluted with water such that it
causes the fibers to coagulate at the proper rate. The main feature
of wet spinning is the mass transfer of solvent; precipitation or
coagulation of the fiber ensues by diffusion of the solvent from the
fiber into the bath, and by diffusion of the water into the thread.
The resulting spin bath liquid contains large amounts of solvent.
This solvent-laden liquid stream is routed to a distillation column
where the solvent is recovered for reuse. Liquid 'streams from the
washing and drawing portions of the process are also treated for
solvent recovery.
The most important aspect of distillation as it affects the
fibers industry is the extreme importance of maximum separation and
recovery efficiency. Since thousands of tons of solvent may pass
through a distillation column at a typical fiber plant within a single
year, even small changes in efficiency would potentially result in the
loss or savings of thousands of dollars.
4.6 ENCLOSURES27
4.6.1 Applicability to the Synthetic Fibers Industry
A major source of VOC emissions at synthetic fiber plants that
utilize an organic solvent to dissolve the polymer is solvent loss
which occurs as the fibers proceed from the exit of the spinning
cabinet through the various texturizing processes. Residual solvent
is volatilized into room and building air at those processing steps
not directly served by the solvent recovery collection system. Room
and building air is, in most cases, then collected by ventilation
systems and either discharged or recirculated in air conditioning
4-21
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systems. In either case, the solvent is maintained at concentrations
well below the lower explosive limit and the threshold limit value for
the particular solvent. These post-spinning fugitive solvent emissions
are eventually directed to the atmosphere. Because enclosures designed
to completely envelope process emission sources so as to collect and
effectively capture solvent vapors are not typically utilized by the
industry as a component of the solvent recovery system, residual
solvent volatilized into the!room and building air is lost to the
process.
One method for reducing;post-spinning fugitive emissions would
involve an,upgrading of ventilation systems serving the fiber processing
lines in order to capture a larger portion of the volatilized solvent.
Collected gas could then be Rented to a control device such as an
absorption scrubber or carbon adsorption system. Enclosure of the
spinning and post-spinning process line with collected gas sent to a
high efficiency control device would likely provide the best system of
emission reduction.
Plant visits conducted during this NSPS development, have shown
that the use of enclosure systems on spinning cell exits and fiber
processing lines in the synthetic fibers industry is technologically
c i ri po on ;
feasible. * ' ' Total enclosure systems in use at existing synthetic
fiber plants are attached to|or comparatively near the source of the
pollutant. Figure 4-5 shows:a spinning machine with one type of
enclosure system. The enclosure functions to reduce the volume of
dilution air required to transport solvent-laden air from the workplace.
The vapor concentration can be controlled so that the control equipment
size and cost are minimized and control efficiency is optimized.
Immediately following the spinning operation, fibers are moved to
and through various process operations. The fiber at and near the
point of exit from the spinning cell contains substantial residual
solvent (as much as 30 percent by weight). This solvent evaporates
into the air surrounding the;process line. As the solvent evaporates,
the vapor-laden air (VLA) can be captured by hooding or enclosures
surrounding that particular process operation. The VLA could be
subsequently moved via ductsj to a control device (scrubber, carbon
bed, etc.) or to an atmospheric discharge point.
4-22
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ENCLOSURE
DOOR
ENCLOSURE
DOOR
\
BASE-OF
SPINNING MACHINE
SIDE VIEW
PROMT VIEW
Figure 4-5. Spinning Machine With Enclosure
4-23
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The amount of solvent which would be ultimately collected by the
control device is a function of several parameters:
1. Control device (scrubber, carbon bed) efficiency,
2. Leakage of VLA from iducting,
3. Air in-leakage to ducting,
4. VLA flow rate, temperature, humidity, i.e., physical parameters
of the VLA itself,
5. Degree of enclosure (how much of the fiber processing line is
enclosed by hooding; how much is open to room air),
6. Design of enclosure ^determines air in-leakage and dilution
of VLA), length of enclosure (determines residence time) and size and
number of worker access doors,
7. Evaporation rate of solvent from the fiber (a function of
several complex parameters, the most significant of which are fiber
type, temperature, physical movement, and concentration of solvent
vapor around the fiber bundle).
Ultimately, each enclosure should be as nearly a "complete enclosure"
as possible with minimum sized openings where access is required. Any
large opening in the capture system should be equipped with a self-closing
door to minimize the amount of dilution air. However, permanent
openings designed to allow air flow and openings used intermittently
for worker access are often necessary. Covers for worker access
openings should be designed to prevent air in-leakage when closed.
t
The entire capture system should be designed in accordance with good
ventilation practice (e.g., Handbook of Ventilation for Contaminant
Control, McDermott; and Industrial Ventilation - a Manual of Recommended
91 on
Practice, ACGIH). 'JU
4.6.2 Safety Considerations of Enclosure Systems'
The three requirements for an explosive mixture are fuel (solvent),
oxidizer (air), and heat. Since the amount of solvent contained
within the fiber as it exits [the spin cell is process-dictated, that
I
value is considered a constant (not a variable for purposes of this
discussion). The velocity arid amount of air into which the solvent
evaporates are variable quantities, up to the limits of the fiber to
i
withstand the impinging air flow. As important from a recovery standpoint
31
4-24
-------
is the limit on air flow posed by the cost of air/solvent vapor treatment
in the recovery device. A compromise is therefore necessary between
the risk associated with higher concentrations, and the costs of
treating larger air volumes.
The most significant factor in explosion/fire prevention within
the recommended enclosures is maintenance of the solvent concentration
at desired levels. Estimates show the concentration within the enclosures,
that will result from application of the recommended control options,
will not approach the LEL for any of the solvents considered. For
example, the flow rate of 15,000 cfm and evaporation rate of about
7 kg/hr of acetone will yield about 3,000 ppm or about 15 percent of
the LEL under normal conditions. If this concentration is not exceeded,
the explosion risk is almost nil. Whether the concentration is allowed
to increase to near explosive levels is critical, however. This can
be prevented by proper design and use of exhaust fans, dampers, monitoring
equipment, etc. An appropriate combination of automatic and manually
operated fail safe measures, plus effective supervision of the equipment
should prevent hazardous situations from occurring.
Solvent-laden air streams which are transported to control equipment
are normally maintained at concentrations at or below 25 percent of
the lower explosion limit (LEL) of the solvent. Although 25 percent
of the LEL is often regarded as the maximum allowable solvent concentration,
insurance and safety requirements will sometimes permit even higher
solvent concentrations. The Handbook of Industrial Loss Prevention
notes that flammable vapor concentrations of up to 50 percent of the
LEL may be tolerated if approved continuous vapor concentration indicator
controllers are used.
The monitors should be set to first adjust the inflow of dilution
air at relatively low concentrations, then activate alarms at higher
concentrations, and finally shut down the spinning machines when unacceptable
levels are reached. Several monitors should be utilized for redundancy
and added safety margin. At some concentration level, perhaps near
the alarm level, operator access doors should be opened, either
automatically or manually when the alarm level is reached. In addition,
power for operation of the exhaust fans should be received from at
4-25
-------
least two independent sources such as electrical power and steam
turbines. Nonelectrical meajns of purging could be utilized as well,
such as steam aspirators or air pressure tanks which could evacuate or
force air/solvent vapors out of the enclosed areas.
Another preventive measure could be the installation of distribution
pipes and nozzles for blanketing the area with either nitrogen or
carbon dioxide when explosivb mixtures are reached. This would both
blanket the area and dilute the potentially explosive vapors. This
system would be effective for both prevention of explosive conditions
and extinguishing of fires once started. There should be some means
of controlling the inert gas or carbon dioxide so that employees are
not overcome.
The ignition of flammable vapors may occur as a result of spark
discharge of static electricity. Changes may be generated by friction
between surfaces such as fibprs and guides, or even by movement of the
fiber through the spin cell atmosphere. The rotating metal take-up
wheels moving against small Quantities of waste fiber could also
generate a static charge or heat from mechanical friction. Protection
against these hazards should! begin with determination of the locations
where static charges are likely generated, and installation or use of
means for gradual dissipation of these charges without spark discharges.
All metal parts, for example!, should be mutually grounded. (Note that
water and steam pipes are unreliable for use as conductors or grounds.)
It has been shown that lexplosions in chemical process plants are
usually the result of nonroutine leakage of flammable materials.
Thus, prevention should incljude strict housekeeping and prompt repair
of leaking lines, particularly lines containing pure solvents or
solvent/water mixtures, or spinning dope. A spill of any of these
would quickly result in flammable air/vapor mixtures above or near the
spill.
There are other relevanjt factors bearing on explosive
characteristics. Decreases in ambient temperature and pressure reduce
the range of flammable mixtures that will ignite. There is also
evidence that increases in filow velocity will decrease the flammable
limits. If the diluent air ris cooled, the explosive range is narrowed
4-26
-------
(LEL increased and UEL decreased). The conclusion is therefore that
if the ventilation inlet air to the enclosures is cooled, moved rapidly,
and/or drawn out under negative pressure, the possibility of ignition
will be reduced. In addition, the reduction in temperature would have
the added effect of causing slower evaporation of acetone from the
moving fibers.
Still another important air conditioning parameter from a fiber
characteristic as well as safety standpoint is humidity. It is important
to keep a minimum of 55 to 60 percent relative humidity, both to
reduce static discharge and to reduce breakage due to brittle fibers.
As a minimum, the design of the process and recovery systems,
particularly the enclosure systems, should consider all the foregoing
preventive measures, and industry experience in reducing the risks of
explosive conditions as far as economically possible. The equipment
and procedures must be able to function not only in normal service,
but especially during emergency or nonroutine periods. Explosive
conditions may be avoided with proper and adequate selection of monitoring
and control instrumentation and adequate supervision of the process
and monitoring equipment.
The use of capture/enclosure devices similar to those described
above, for use on synthetic fiber spinning and processing lines, have
also been recommended in other studies regarding specific segments of
the fibers industry. These studies have received considerable review
by the industry. They include:
• Economic Impact Assessment for Acrylonitrile
by Enviro Control, Inc., Contract No. J-9-F6-0229, February 21,
1978, for Occupational Safety and Health Administration
• U.S. Department of Labor Emission, Process, and Control
.Technology Study of the ABS/SAN, Acrylic Fibers, and NBR
Industries, by Pullman Kellogg, Contract No. 68-02-2619,
April 20, 1979,. for ESED, OAQPS, U.S. Environmental Protection
Agency.
4.7 INCINERATION32'35
An alternative means of reducing VOC emissions, other than by
increasing the solvent recovery efficiency, is incineration of the
4-27
-------
solvent vapor. Incineration! control devices operate on the principle
of combustion, through oxidation of gas stream constituents into
(primarily) products of carbon dioxide and water. Process exhaust
streams which flow into the incinerator will likely be below 25 percent
of the LEL. Hence, to effectively accomplish combustion, fuel must be
added to the diluted vapor before incineration occurs. Devices which
add fuel to diluted vapor streams and incinerate the combined stream
are referred to as afterburners. Other energy needs within the plant
can often be supplemented by the heat produced during combustion. Two
types of afterburners may be used to reduce process emissions, direct
flame (thermal) and catalytic oxidizers.
Thermal incinerators consist of a mixing chamber designed to
provide contact between the [vapor-laden gas stream and the burning
flame, followed by a combustion chamber. The efficiency of a thermal
afterburner is affected by the air-fuel-vapor concentration ratios,
residence time required for complete combustion, and sufficient tempera-
ture to ensure complete oxidation of the combustibles. Burner type
and placement also determine thermal afterburner efficiency. Multi-jet
and mixing-plate burner types prove most effective in maximizing flame
and vapor-laden air content. Incomplete combustion of gas constituents
may permit carbon monoxide, aldehydes, or other reactive compounds to
be exhausted from the unit.| Natural gas, LPG, and distillate and
residual fuel oils are used\ to fuel afterburners and create the potential
for reactive halogens, sulfur oxides, and organic acids to be exhausted
into the atmosphere if low combustion efficiencies are encountered.
Figure 4-6 shows the design features of a direct flame afterburner.'
The design of catalytic afterburners is similar to direct flame
(thermal) units except that combustion is initiated through use of a
catalyst.. A catalyst is a substance that changes the rate of a chemical
reaction without altering the composition of the catalytic material.
Catalytic afterburners employ a solid active surface' on which the
combustion process occurs. Preheated process gases are directed
through a heated catalytic bed, usually a honeycomb network of platinum
or palladium, which promotes oxidation. Thin layers of the catalytic
metal are deposited on an inert substrate of variable shape. The
36
4-28
-------
FLAME SENSOR-
BURNER.
REFRACTORY-
INSULATION-
TURBULENT EXPANSION ZONE-
STEEL SHELL —
STRAIGHTENING
VANES
COOLIN6 AIR
INDUCTION SYSTEM
CAS SYSTEM
control
-CONTROL PANEL
(roraot* optional)
UNITIZED MOUNTING
•SAMPLE PORT
TEMPERATURE SENSOR
-BLOWER
-INSULATION
Figure 4-6. Sectional View of Direct-Flame Afterburner3
4-29
-------
37
catalytic material provides a large surface area containing active
sites upon which the gas molecules can react. Catalytic afterburners
thus require less fuel and operate at lower temperatures than direct
flame types.
Maintenance for catalytic systems is frequent. Certain constituents
of the process gas stream such as polymeric compounds or particulates
may not burn properly, causing a buildup on the substrate and thereby
deactivating the catalyst. Various cleaning methods to remove such
coatings will reactivate the catalytic material. The catalyst may
also be deactivated through clirect reactions with phosphorous, sulfur,
and heavy metals present in the effluent gas stream. In an effort to
minimize operational problem?, inlet gas stream concentrations are
usually limited to 25 percent of the LEL and ignition temperatures
maintained between 540° to 650°C (1000 to 1200°F). Figure 4-7
illustrates the use of catalytic incinerators for heat recovery.
VOC control efficiencies of direct flame afterburners can reach
98 percent; catalytic afterburner VOC control efficiencies are reported
to be between 81 and 96 percent. Effectiveness of incineration
technology in reducing VOC emissions is dependent upon: the vapor
ignition temperature; chamber size and turbulence; effluent flow rate;
as well as afterburner design. Typical design flow rates for
i
direct-flame afterburner packages range from 250 to 50,000 scfm/unit,
while catalytic afterburners'are designed to accommodate flow rates
ranging from 400 scfm to 40,000 scfm. Custom-built units, capable of
handling larger flow rates, are available. However, industry-supplied
data indicate that conventional packaged designs are suitable for
treating typical process exhaust streams.
Incineration is an emission control technique that could be used
to reduce.VOC emissions from!the synthetic fibers industry. Presently,
however, synthetic fiber facilities do not utilize the option of
incineration to control V.OC's. Primarily this is because existing
control equipment was installed to recover increasingly expensive
solvent for the purpose of cost optimization. Incineration is a
destructive method of emission control directly opposing solvent
reclamation efforts. The results of a study which examined the economic
4-30
-------
01SCK1R6E TO ITHOSPHERE
'l
RETURN TO OVEN-*
-P£BFOR«TEO PL«TE
PREHEIT BUBNEBS
Catalytic incinerator utilizing direct-
heat recovery
•DISCHARGE TO ATMOSPHERE
PERFORATED PLATE
Catalytic incinerator utilizing indirect
heat recovery
Figure 4-7. Catalytic Incinerators Utilizing Heat Recovery
4-31
-------
feasibility of incineration as a VOC control technique in the synthetic
; 00 30
fibers industry appear to substantiate this claim. ' In the report,
six individual incineration systems were analyzed to determine capital
and annual operating cost. The six systems included three separate
cases; each case was analyzed for both thermal and catalytic Incinerators.
The Case 1 situation involved incineration with no recuperative heat
recovery. Case 2 represented incineration with primary heat recovery
at an efficiency of 35 percent. Case 3 involved the use of primary
heat recovery at 35 percent efficiency and secondary recovery at
55 percent efficiency. The six incineration systems were then compared
with the cost of a low and high efficiency carbon adsorption system.
The result of the study indicated that the cost of incineration is
significant; and when compared with a solvent recovery system, such as
a carbon adsorption system, incineration does not appear to be an
economically viable control option for the synthetic fibers industry.
Other disadvantages to incineration include:
• Fuel is continuously Burned regardless of whether the exhaust
stream is intermittent or has fluctuating concentrations;
• Incompletely combusted VOC's including the auxiliary fuel may
be potent smog precursors;
• Secondary air pollutants (NO , SO , CO) present in afterburner
X X
exhaust, may contribute to air pollution problems;
• Low sulfur content fuels are recommended for operation of
incinerators; however, these fuels are expensive and not always available.
• The energy impacts required to raise the contaminant air
stream to 1,500°F may be significant.
• Gas streams with very low VOC concentration may require
significantly more fuel to achieve temperatures around 1,500°F.
4.8 EMISSION AND PROCESS TESTING
Volatile organic compound (VOC) emissions were the principal type
i
of air pollutant encountered during the testing of emissions from
fiber producing plants. These emissions result primarily from organic
solvents used during fiber producing operations. Processes tested
under the emission measurement program utilized either dimethylformamide
(DMF) or dimethylacetamide (DMAc) as the spinning solvent.
4-32
-------
Baseline emission values have been determined by combining and
reducing data obtained from a variety of sources. By integrating
Information acquired through literature searches, EPA 114 responses,
plant surveys, and emission test data, mass balance calculations have
been performed. For the purpose of determining a plant's compliance,
there are two methods theoretically available for calculating emissions:
direct measurement of emissions and indirect determination by mass
balance.
Two sites were chosen for field testing for direct measurement of
VOC emissions. One plant operated a dry spinning process, whereas the
other plant operated a wet spinning process. Vents and stacks were
identified and prioritized according to the relative amount of VOC's
emitted to the atmosphere. In order to determine solvent vapor
concentrations and distribution within enclosures such as those described
in Section 4.6, testing was performed at one plant that already utilizes
this type capture technique. Emission test reports have been issued
and describe in full the testing procedures and methods employed (see
Appendices C and D).
In addition to direct measurement of VOC's via field testing, EPA
also obtained solvent use information from six different fiber plants
covering the previous 2 years (1979-1981). The solvent use information
can be indirectly used to determine VOC emission rates, since makeup
flow rates are exactly equivalent to the total of nongaseous losses
(as determined by prior actual measurements) and air emissions. This
solvent use data is summarized in Appendix C. The amount of makeup
solvent is measured by totalizing flow meters, an inexpensive, simple,
and continuous method of indirectly determining VOC emissions.
4.9 SUMMARY
A description of the solvent capture and recovery techniques
presently employed in the synthetic fibers industry was presented in
this chapter, and five techniques employed in the synthetic fibers
industry to recover solvent from wet, dry, and reaction spinning
processes were outlined. They include gas absorption, gas adsorption,
condensing, distillation, and enclosure and capture systems.
4-33
-------
Table 4-2 summarizes the more common recovery process technologies
currently in use in the industry, along with the fiber types utilizing
these techniques.
4-34
-------
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4.10 REFERENCES
1. Moncrief, R.W. Man-Made!Fibres. Newnes-Butterworks. London,
Boston. 1975. ;
2. Air Pollution Engineering Manual. Air Pollution Control District
County of Los Angeles. U.S. Environmental Protection Agency.
Research Triangle Park, N.C. Publication No. AP-40. May 1973.
pp. 207-229.
3. Radian Corporation. Control Techniques for Volatile Organic
Emissions from Stationary Sources. U.S. Environmental Protection
Agency. Research Triangle Park, N.C. Publication No. EPA-450/2-78-022.
May 1978. pp. 70-83.
4. Perry, R.H. and C.H. Chitton. Chemical Engineers' Handbook,
Fifth Edition. McGraw-Hill Book Company, Incorporated.
New York, New York. 1973.
5. Control Techniques for Hydrocarbon and Organic Solvent Emissions
from Stationary Sources. U.S. Public Health Service. Washington,
D.C. Publication No. AP-68. March 1970. 114 p.
6. Report of the Initial Plant Visit to Tennessee Eastman Company
Synthetic Fibers Manufacturing Facility in Kingsport, Tennessee.
Prepared during Development of New Source Performance Standards
for the Synthetic Fibers Industry'. December 13, 1979.
7. Letter arid attachments from Mohney, W.K., Avtex Fibers, Incorporated,
to Manley, R.9 Pacific Environmental Services, Incorporated.
April 14, 1981. Response to Section 114 information request.
8. Report of the Phase II Plant Visit to Celanese Fibers Company
Celco Acetate Fiber Plant in Narrows, Virginia. Prepared during
the Development of New Source Performance Standards for the
Synthetic Fibers Industry. August 11, 1980.
9. Letter and attachments from Pullen, J.C., Celanese Fibers Company, ,
to Zerbonia, R.A., Pacific Environmental Services, Incorporated.
July 3, 1980. Response'to Section 114 information request (Celco
Acetate Fiber Plant, Narrows, Virginia).
10. Report of the Phase II Plant Visit to Celanese Fibers Company
Celriver Acetate Plant in Rock Hill, South Carolina. Prepared
during the Development of New Source Performance Standards for
the Synthetic Fibers Industry. May 28, 1980.
11. Letter and attachments from Pullen, J.C., Celanese Fibers Company,
to Zerbonia, R.A., Pacific Environmental Services, Incorporated.
July 3, 1980. Response to Section 114 information request (Celriver
Acetate Fiber Plant, Rock Hill, South Carolina).
4-36
-------
12. Welters, E. Process and Machine Technology of Man-made Fiber
Production. International Textile Bulletin. World Edition.
February 1978. pp. 153-262.
13. Memorandum and attachments from Gladding, D.., Pacific Environmental
Services, Inc., to Grumpier, D., and Chaput, L., U.S. Environmental
Protection Agency. November 3, 1981. Impacts of Possible Reduction
of the Threshold Limit Value (TLV) for Acetone on Cellulose
Acetate Fiber Manufacturers.
14. Bethes, Robert M. Air Pollution Control Technoloc
Reinhold Company. New York, New York. 1978 p. 31
Van Nostrand
15. Hydrocarbon Pollutant Systems Study, Volume I - Stationary Sources,
Effects and Controls. U.S. Environmental Protection Agency.
Research Triangle Park, N.C. Publication No. APTD-1499. October
1972. 377 p.
16. Reference 3. pp. 52-70.
17. Reference 2. pp. 189-198.
18. Grant, R.M., M. Manes, and S.B. Smith. Adsorption of Normal
Paraffins and Sulfur Compounds on Activated Carbon. AICHE Journal.
J3(3):403. 1962.
19. Surface Coating of Metal Furniture. Background Information of
Proposed Standard - Draft EIS. EPA 450/3-80-007a. September
1980.
20. Trip Report. Plant Visit to Globe Manufacturing Company, Gastonia,
North Carolina. September 16-17, 1981.
21. McDermott, H.J. Handbook of Ventilation for Contaminant Control.
Ann Arbor Science Publishers, Inc. Ann Arbor, Michigan. 1976.
368 p.
22. Control of Volatile Organic Emissions from Existing Stationary
Sources - Volume I: Control Methods for Surface-Coating Operations.
U.S. Environmental Protection Agency. Research Triangle Park, NC.
Publication No. EPA 450/2-76-028. November 1976. 166 p. ,
23. VIC Manufacturing Company. Carbon Adsorption/Emission Control -
Benefits and Limitations. Minneapolis, Minnesota, p. 7-8.
24. Letter and attachments from Wieland, K. and Waldrop, R., Edwards
Engineering Corp., to Manley, R., Pacific Environmental Services,
Inc. January 15, 1982. Use of Condensers for Organic Vapor
Recovery.
25. Reference 3. pp. 83-92.
4-37
-------
26. Reference 4. pp. 13-19 to 13-24.
27. Memorandum and addendumifrom Manley, R., Pacific Environmental
Services, Inc., to Grumpier, D., et.al., U.S. Environmental
Protection Agency. October 2, 1980. Capture Efficiencies of
Enclosures and Impact on the NSPS Development for the Synthetic
Fibers Industry.
28. Report of the Initial Plant Visit to DuPont Corporation May
Plant, Camden, S.C. Prepared during development of New Source
Performance Standards for the Synthetic Fiber Industry. April 29,
1980.
29. Report of the Plant Visit to American Enka Company Viscose Rayon
in Lowland, Tennessee. Prepared during development of New Source
Performance Standards for the Synthetic Fiber Industry,, January 22,
1980.'
30. Industrial Ventilation: A Manual of Recommended Practice, Twelfth
Edition. American Conference of Governmental Industrial Hygienists.
Committee on Industrial Ventilation. Lansing, Michigan. 1972.
337 p. :
31. Memorandum and attachments from Manley, R., Pacific Environmental
Services, Inc., to Grumpier, D. and Chaput, L., U.S. Environmental
Protection Agency. December 8, 1981. Discussion of Potential
Safety (Explosion) Problems Associated with the Use of Enclosures.
i
32. Report, of Fuel Requirements, Capital Cost and Operating Expense
for Catalytic and Thermal Afterburners. CE Air Preheater Industrial
Gas Cleaning Institute. Stamford, Conn. EPA Report No. EPA-
450/3-76-031. September 1976.
33. Memorandum and addendum from Mascone, D., EPA to Farmer, J.,
EPA/CPB, Office of Air Quality Planning and Standards. June 11,
1980. Thermal Incinerator Performance for NSPS.
34. Reference 2. pp. 437-531.
35. Reference 3. pp. 24-52.
36. Large Appliance Surface Coating Industry - Background Information
for Proposed Standards. •• U.S. Environmental Protection Agency.
Research Triangle Park, N.C. June 6, 1980. p. 4-8.
37. Reference 36. p. 4-9. ;
38. Air Pollution: Control Techniques for Hydrocarbon and Organic
Solvent Emissions from Stationary Sources. NATO Committee on the
Challenges of Modern Society. Brussels, Belgium. October 1973.
39. Memorandum and attachments from Zerbonia, R.A., Pacific Environmental
Services, Incorporated, to Docket No. A-80-7. November 10, 1981.
Control Costs and Regulatory Alternative Development for Reaction
Spun Spandex Fiber Process (Carbon Adsorption vs. Incineration).
4-38
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5.0 MODIFICATION AND RECONSTRUCTION
5.1 BACKGROUND
Emission limitation standards promulgated under Section lll(b) of
the Clean Air Act apply to all facilities within the regulated source
category that are constructed, modified, or reconstructed after the
date of proposal of the standards. Uncertainties may arise as to the
determination of whether any existing facility has been "modified" or
"reconstructed." These issues are addressed in Sections 60.14 and
60.15, respectively, of Title 40 of the Code of Federal Regulations,
which defines conditions under which an "existing facility" may become
1 2
subject to standards of performance. * An "existing facility,"
defined in 40 CFR 60.2(aa), is an apparatus of the type for which a
standard of performance is promulgated and the construction or modifi-
cation of which was commenced prior to the date of proposal of that
standard.
The following discussion examines the applicability of the
modification/reconstruction provisions to any facilities for the
manufacture or processing of synthetic fibers in existing fiber manufac-
turing plants, and details conditions under which existing facilities
could become subject to standards of performance for new stationary
sources. The enforcement division of the appropriate EPA regional
office should be contacted regarding any questions on modification or
reconstruction applicability.
5.2 40 CFR PART 60 PROVISIONS FOR MODIFICATION AND RECONSTRUCTION
5.2.1 §60.14 Modification
§60.14 states:
". . ., any physical or operational change to an existing facility
which results in an increase in the emission rate to the atmosphere
of any pollutant to which a standard applies shall be considered
5-1
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,,1
a modification within the meaning of Section 111 of the Act.
Upon modification, an existing facility shall become an affected
•facility for each pollutant to which a standard applies and for
which there is an increase in the emission rate to the atmosphere.
Paragraph (b) clarifies what constitutes an increase in emissions
in kilograms per hour and the procedures for determining the increase
including the use of emission factors, material balances, continuous
monitoring system and manualiemission tests. Paragraph (c) affirms
that the addition of a facility subject to performance standards to a
stationary source does not make any other facility within that source
subject to standards of performance. Paragraph (f) simply provides
for superseding any conflicting provisions.
Paragraph (e) lists cerjtain physical or operational changes which
by themselves are not considered modifications. These changes include:
(1) Facility maintenance, repair, and replacement which are
determined by the Administrator to be routine.
(2) An increase in the!production rate not requiring a capital
expenditure as defined in §60.2(bb).
(3) An increase in the!hours of operation.
(4) Use of an alternative fuel or raw material if prior to the
standard, the existing facility was designed to accommodate that
alternate fuel or raw material. (Conversion to coal, as specified in
§lll(a)(8) of the Clean Air Act, is also exempted.)
(5) The addition or use of any system or device whose primary
function is the reduction of air pollutants, except when an emission
control system is removed or| replaced by a system considered to be
less efficient.
(6) The relocation or change in ownership of an existing facility.
An increase in the production rate of an existing facility is
designated as a modification only if there is an increase in the
emission rate and the total jcost necessary to accomplish the change
constitutes a "capital expenditure." Capital expenditure is the
product of the facility's original cost, as defined by Section 1012 of
the Internal Revenue Code, and the appropriate "annual asset guideline
5-2
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repair allowance percentage" (AA6RAP). The 1978 edition of Internal
Revenue Service Publication 534 sets the AA6RAP for the synthetic
fiber manufacturing industry at 16 percent. Therefore, if the total
cost of increasing the production rate of an existing synthetic fiber
manufacturing facility exceeds 16 percent of the facility's original
cost, and if this change causes increased emissions, the facility
would be considered to have been modified.
5.2.2 §60.15 Reconstruction
§60.15 states:
"An existing facility, upon reconstruction, becomes an affected
facility, irrespective of any change in emission rate. 'Recon-
struction' means the replacement of components of an existing
facility to such an extent that: (1) the fixed capital cost of
the new components exceeds 50 percent of the fixed capital cost
that would be required to construct a comparable entirely new
facility, and (2) it is technologically and economically feasible
2
to meet the applicable standards set forth in this part."
Reconstruction, as defined in 40 CFR 60.15, occurs when the fixed
capital cost of replacement components of an existing facility exceeds
50 percent of the fixed capital cost that would be required to construct
a comparable entirely new facility, and it is technically and economically
feasible to meet the applicable standards. After receiving notice
from the owner or operator as required under 40 CFR 60.15(d), the
Administrator will determine whether the proposed replacement constitutes
a reconstruction. In accordance with 40 CFR 60.15(f), the Administrator's
decision is based upon the following: (1) the fixed capital cost of
the replacement components, (2) the estimated life of the facility,
(3) the extent to which the components being replaced cause or contrib-
ute to the emissions from the facility, and (4) any economic or
technical limitations on compliance that are inherent in the proposed
replacements. Investigation of the synthetic fibers manufacturing
industry does not reveal any history of changes that ^ould render a
line subject to the reconstruction provision. Repair or rebuilding of
an existing facility where costs would exceed 50 percent of the cost
of replacing the facility would be unusual.
5-3
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5.3 APPLICABILITY TO SYNTHETIC FIBER MANUFACTURING PLANTS
5.3.1 General
Investigation of the processes used by manufacturers of synthetic
fibers does not reveal any particular practice which can be readily
classified as a modification or reconstruction. A number of potential
actions have been identifiedjwhich, under certain circumstances, may
indeed be so classified. The following sections are concerned with
alterations common to those process facilities which would be affected
by the application of the modification and reconstruction provisions.
In Sections 5.3.2 and 5.3.3, other practices specific to each process
facility are discussed.
5.3.2 Modifications
Investigation of the processes used by manufacturers of synthetic
fibers does not reveal any particular practice, other than the direct
addition of production equipment, which can be readily classified as a
modification. There are, however, a number of routine alterations
common to synthetic fiber production facilities which would not likely
be affected by the application of the modification provision, even
though many of these changes|can affect solvent emissions, some positively
and some negatively. Some examples are: changes in fiber properties
i
such as denier; variation injdrawing, washing, and stretching operations;
routine alterations in co-polymer to co-polymer and polymer to solvent
ratios; changes in additives and finishing oils; and normal variation
in spin and wash bath temperatures. Any increase in VOC emissions
effected by these routine changes in the manufacturing process would
not be considered a modification since they are considered to be
within the normal operation of a facility as designed.
5.3.2.1 Production Rate Increases. An increase in production
rate at an existing facility|is not in and of itself a modification
under §60.14 if the increase!can be accomplished without incurring a
capital expenditure at the affected facility.* If a capital expenditure
*Capital expenditure is defined as "an expenditure for a physical or
operational change to an existing facility which exceeds the product
of the applicable annual asset guideline repair allowance percentage
specified in the latest edition of Internal Revenue Service Publica-
tion 534, and the existing facility's basis, as defined by Section 1012
of the Internal Revenue Code." (40 CFR 60, Sect. 60.2[bbj).
: 5-4
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less than the product of the most recent annual asset guideline repair
allowance published by the Internal Revenue Service (Publication 534)
and the facility's basis is made to increase capacity at an existing
facility and also results in an increase in emissions of a regulated
pollutant to the atmosphere, a modification is not considered to have
A
occurred. Any fiber manufacturing plant is designed for a maximum
production capacity, which is directly related to the maximum capacity
of the spinning cells and the number of these spinning cells or cabinets.
Process stages other than spinning (e.g., dissolving/blending or
drying) may have capacities which exceed the total plant capacity for
finished fiber. Thus, an increase in the production capacity of a
plant is possible without a capital expenditure if only those facilities
which limit fiber production (de-bottlenecking) are modified. For
example, an increase in the plant production capacity might be
accomplished by changing from batch processing to continuous processing
or the addition of spinning cabinets (or spinnerets). If the additional
line(s) were part of a facility for which NSPS are established, it
would be subject to NSPS if the addition caused an increase in VOC
emissions and if the capital expenditure criteria were met.
5.3.2.2 Change in Raw Materials. A modification in the polymer
and/or co-polymer introduced into the process will likely have a minor
effect on the solvent (VOC) emissions. The change in emissions would
probably not be measurable, and the overall effect would be negligible.
Changes in solvent use practices may result in a rise of the VOC
emission rate from fiber manufacturing facilities. One possible
change would be an increase in the volatility of the solvent caused by
temperature increases. This would result in an increase in the quantity
of VOC emitted per unit of product. Another change would be the use
of solvent with a lower boiling point, although this change of solvent
within a plant is not common in the industry.
Another possible change would be to increase the ratio of solvent
used per unit of product. This change might be necessitated for
desired product characteristic changes. This would create an additional
load on the solvent recovery system while maintaining constant product
5-5
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output. Additionally, increasing solvent used per unit of fiber
produced would increase costs of solvent recovery and cost per unit of
fiber.
A further change which would affect VOC emissions would be a
change in water (or other solvent) content of the primary solvent,
thus altering the boiling pojint of the mixture. This is more likely
to actually occur within the| industry, although the net change in VOC
emission would be very small>
These changes would not! likely be considered to be modifications
and would not cause the facility to be subject to the standard(s),
because the changes primarily involve a switch in raw material which
the facility was designed to accommodate.
5.3.2.3 Alternative Fuel. The use of an alternative fuel would
not be considered a modification if the existing facility were designed
to accommodate the alternative.
5.3.2.4 Addition of a System to Control Air .Pollutants. The
addition or use of any system or device whose primary function is to
reduce air pollutants, excepjt the replacement of such a system or
device by a less efficient one, is not by itself considered a modi-
fication under §60.14. For example, the replacement of a relatively
inefficient scrubber with a fnore efficient scrubber in an existing
installation, for the purposje of improving solvent recovery (solvent
that would otherwise be emitted to the atmosphere) would not be considered
a modification under §60.14(e)(5).
5.3.2.5 Maintenance, Repair, and Replacement. Maintenance,
repair, and component replacement which are considered routine for a
source category are not considered modifications under §60.14(e)(1).
An increase in emissions is Inot expected to occur as a result of
normal maintenance or replacement of fiber production components.
Routine maintenance would involve periodic cleaning, replacement
i
of parts, and lubrication of moving parts. Routine maintenance should
not have any noticeable effect on emissions, since VOC is introduced
to the system only when the process is in operation.
Several components can be expected to require replacement as a
matter of routine due to the unit being in continuous service for long
periods of time. These components may include spinneret heads, fiber
5-6
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guides, scrubber nozzles, and drive gears. Replacement with equivalent
components should not affect emissions and would be considered exempt
under §60.14(e)(l).
5.3.2.6 Equipment Relocation and Change of Ownership. Relocation
of equipment would not constitute a modification.
5.3.2.7 Removal or Disabling of a Control Device. The intentional
removal or disabling of any emission control component of an existing
installation which would cause an increase of emissions would be a
modification. An existing facility that is modified becomes an affected
facility subject to the NSPS.
5.3.3. Reconstruction
The term reconstruction means the replacement of components to an
extent that the fixed capital cost of the new components exceeds
50 percent of the fixed capital cost that would be required to construct
a comparable, entirely new facility (40 CFR 60.15). Repair or rebuilding
of an existing facility at a cost exceeding 50 percent of the cost of
an entirely new facility is unusual. There are no general conditions
which can be classified as a reconstruction. As stated previously,
production rate increases are usually met by adding new lines to
existing facilities rather than rebuilding lines in existing facilities.
The one common exception is conversion of cellulose acetate textile
yarn capacity to filter tow capacity. Determination of whether any
repair or rebuilding activities constitute reconstruction must be made
by the Administrator on a case-by-case basis.
If a previously closed plant were to reopen, it would not be
subject to NSPS unless one or more of the facilities for which standards
had been promulgated were altered sufficiently to meet reconstruction
criteria. Then, only those facilities which had been altered and for
which standards exist would be subject to NSPS.
Determination of reconstruction is based on the capital cost of
all new construction and other technical and economic considerations.
The Administrator will consider if it is technically and economically
feasible to meet the applicable standards in making any reconstruction
determination. For synthetic fiber production facilities, retrofitting
solvent recovery equipment to existing plants can pose certain problems.
5-7
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The amount of physical space .necessary to install ventilation and
ductwork to capture solvent from process lines is a definite constraining
factor. Equipment and personnel must be able to move down process
line aisles without being hindered; therefore, installation of enclosures
at some existing facilities may not be possible without a complete
reconstruction of the entire spinning area.
Also, the cost of installing a control system in an existing
plant is greater .than the cost of the systan for a new facility with
the same exhaust gas parameters because of special design considerations.
In retrofitting systems, additional costs may be encountered because
of such items as demolition requirements, crowded construction working
conditions, scheduling construction activities with production activities,
and longer inter-connecting piping. These constraints must be taken
into account when costing the retrofitting of recovery equipment at
synthetic fiber plants. Availability of space, additional ducting,
i
and additional engineering mijst also be considered.
Configuration of equipment in the existing plant governs the
location of the control system. Depending on process or stack location,
long ducting runs from ground level to the control device, stack, and
reprocessing equipment may be required. Costs may increase considerably
if the control equipment must be placed on the roof and requires steel
structural support. It is estimated that rooftop installation can
double the installation costs.
5.3.4 Cellulose Acetate Filament Production Change to Filter Tow
Production
An alteration in cellulose acetate production which would possibly
qualify as modification or reconstruction is the change from cellulose
acetate filament production to cellulose acetate filter tow production.
The changes necessary to alter a given filament process line to permit
filter tow production would be the removal of bobbin winding equipment
and the addition of one or more fiber crimpers arid dryers. Also, a
finishing step would be added (prior to the crimping step) to provide
desired fiber characteristics.
The spinning step would |be essentially unchanged, and of the
\
total VOC released., most of the volatilized VOC is generated at this
5-8
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step. Therefore, the changes in the post spinning processing steps
will affect only the residual solvent content of the fiber after the:
spinning step. Whereas VOC was released relatively slowly into the
room air from the bobbins, containing filament yarn, the filter tow
process line addition of a dryer should cause a major portion of the
solvent to be released in the heated drying area, which would be more
easily collected and controlled. The total solvent ultimately released,
however, would be essentially the same in both cases; only the rate of
release from a given mass of fiber would be changed, if the dryer were
uncontrolled.
5-9
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5.4 REFERENCES ;
1. U.S. Environmental Protection Agency. Code of Federal Regulations.
Title 40, Protection of Environment, Section 60.2(h), Definitions.
Washington, D.C. Office of the Federal Register. Revised as of
July 1, 1977. p. 6.
2. U.S. Environmental Protection Agency. Code of Federal Regulations.
Title 40, Protection of Environment, Section 60.15, Reconstruction.
Washington, D.C. Office of the Federal Register. July 1, 1977.
p. 18.
3. Tax Information on Depreciation. U.S. Department of the Treasury.
Internal Revenue Service. Washington, D.C. Publication 534.
1978. .p. 29.
4. Standards of Performance for New Stationary Sources. Subpart A,
40 CFR 60.15 (44 FR 55173).
5-10
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6.0 MODEL PLANTS AND REGULATORY ALTERNATIVES
Model plants are parametric descriptions of the types of plants
that, in EPA's judgment, will be constructed, modified, or reconstructed.
The model plant parameters form the basis for estimating the environmental,
economic, and energy impacts associated with the application of the
regulatory alternatives to the model plants. Regulatory alternatives
are ways in which EPA could regulate emissions from solvent-spun
synthetic and semisynthetic fiber manufacturing plants. This chapter
will define the model plants and identify the regulatory alternatives
as applied to synthetic fiber manufacturing plants..
6.1 MODEL PLANTS1"6
The model plants chosen to represent the portion of the synthetic
fibers industry under consideration for new source performance standard
(NSPS) development are described in this chapter. This study concentrates
on the production processes which involve the spinning (extrusion) of
the fiber from a solution of polymer or prepolymer and organic solvent(s).
All fiber spinning processes share certain fundamental similarities.
Basically, the object is to extrude a liquid or semi-solid polymer in
a desired cross section and then solidify it before mechanically
taking it up with a collection device. In most processes the solid
fiber is subjected to further mechanical processing to enhance its
properties; in others, the fiber is taken up essentially as a finished
product. Those broadly identifiable process stages which are common
to all solvent-spun synthetic fiber processes include: (1) preparation
of the spinning solution. In this stage, polymer is dissolved in an
organic solvent; the solution is blended with additives and filtered
to complete the preparation of the dope for spinning. (2) Spinning of
the fiber, that is, the actual formation of the fiber filaments.
Polymer solution (or dope) is forced or extruded through a device
called a spinneret to create the fiber. (3) Processing of the
6-1
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formed fibers. This might include lubrication, washing,, drying, heat .
setting, finishing, or crimping. (4) Solvent recovery. Because of
the large amounts of sol vent |used (a pound of polymer is typically
dissolved in 2 to 3 pounds of solvent), the economics of the industry
require that almost all of the solvent used in dissolving be recovered
for reuse. Typically, solvent is recovered most efficiently and
economically at the spinning step from the spin-cells or spin baths
into which polymer solutions are extruded. About 94 to 97 percent of
the solvent used is recycled directly from the spinning step alone.
Thus, a primary solvent recovery system is an integral part of all
solvent spinning processes. iFigure 6-1 presents a general iz:ed process
flow diagram illustrating these common production stages.
Beyond the similarities, there are many differences among processes.
Besides having a stable commodity fiber-producing portion, the industry
is also comprised of a relatively dynamic specialty fiber-producing
portion, into which new fiber types and production, methods are frequently
being introduced. Still other solvent-spun types are being produced
at pilot scale levels, and may or may not expand to full production
(solvent-spun rayon, for example). Consequently, production parameters,
such as fiber spinning rates, processing sequences, and polymer/solvent/
fiber processing ratios that ;vary from one fiber producer to another
and sometimes within each plant lead to a wide variety of fiber types
and production methods for which model plants could be developed.
Thus no single model plant could adequately characterize the
organic solvent-spun synthetic fibers industry, since each synthetic
fiber manufacturing process is unique. It would be nearly impossible
to develop a model plant and |associated economic analysis for each
conceivable fiber type. Therefore, several model plants were developed
such that any organic solvent-spun fiber process (currently existing
or unknown) could be technically represented by one of them,,
This chapter presents five model plants and two basic fiber types
for technical analysis. The five model plants were developed to
represent the differences in^spinning operations due to resin type,
the spinning processes, and the fiber processing stages subsequent to
the spinning step. Selection of specific model plant operating parameters
6-2
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were based on published literature, information obtained during plant
visits, and industry responses to EPA requests for information. This
information, as well as material balance calculations and EPA-conducted
emission tests, was used to develop baseline emission factors.
The model plants were selected to be representative of basic
organic solvent-spun manufacturing processes and not individual fiber
plants. However, in order to provide a basis for economic analysis,
data regarding fiber type and spinning solvent were assigned to each
model plant. In this regard.the model plants represent wet-spun
acrylic, dry-spun acrylic, dry-spun modacrylics, dry-spun acetate
filter tow, and dry-spun acetate filament and staple. Model plants
were then developed as parametric descriptions of the types of plants
that in EPA's judgment are most likely to be constructed, modified, or
reconstructed. The model plant parameters are summarized in Table 6-1.
As noted above, the model plants can be classified as representative
of two basic fiber types: acrylic and modacrylic fibers, which cover
all fibers consisting of at least 85 percent and 35 percent polymerized
acrylonitrile, respectively; and cellulose acetate fibers, which cover
i
all cellulosic fibers having a percentage of acetylation of 15 percent
or greater (includes triacetate).
During the course of this study, model plants were also developed
to characterize spandex fibers. Spandex is a manufactured fiber in
which the fiber-forming substance is a long chain synthetic polymer
comprised of at least 85 percent of a segmented polyurethane. Spandex
is manufactured with two different processes domestically; one, a
reaction-spinning process, is a substantially different process than
any used for other fiber types by any manufacturer in the U.S. The
second process used in the production of spandex is the conventional
dry-spinning process which in some respects is similar to that used
for acetate textile yarn; the fiber is dry spun and immediately wound
onto take-up bobbins, then twisted or processed in other ways. In the
development of the model plants for these spandex processes, it was
not possible to identify technically demonstrated or economically
viable methodology that conclusively reduced emissions (or improved
solvent recovery) over existing baseline conditions. There are no
more stringent control optiojns or regulatory alternatives available
6-4
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for these fiber processes. This precludes the need for the development
of an economic analysis for the spandex processes at this time.
Therefore, the model plants and related information regarding the
I
spandex processes were not included in this chapter of the BID but
; 7-13
have been placed in the public idocket for examination.
It should be noted that in all model plant cases a solvent recovery
system is included as an integral part of the process. This solvent
recovery system is essential for the economic operation of all solvent-spun
synthetic fiber production facilities.
6.2 REGULATORY ALTERNATIVES14729
The purpose of this section is to define various regulatory
alternatives or possible courses of action EPA could take to reduce
i
VOC emissions from the synthetic fibers industry. The regulatory
alternatives were developed following the study of the synthetic
fibers industry and the available control techniques. Section 111 of
the Clean Air Act, as amended, requires that standards of performance
reflect the degree of emission!control achievable through application
of the best demonstrated technological system of continuous emission
reduction which (taking into consideration the cost of achieving such
emission reduction, any nonair[quality health and environmental impact,
and energy requirements) has been adequately demonstrated.
The most effective emission control technology currently used in
the industry involves capture of a large portion of the solvent vapor
generated during fiber manufacture by enclosing entire segments of the
process line. The enclosures Were originally designed and constructed
in such a way as to minimize infiltration of solvent vapor into room
air in order to prevent worker exposure as well as minimize the capture
and unnecessary treatment of uncontaminated room air. This technology
(referred to as Control Option A) can be applied to corresponding
process stages in all wet and dry solvent-spun fiber manufacturing
facilities. When applied to process stages which typically emit the
largest amounts of solvent vapor (e.g., spin cell exits or fiber
dryers), emission reductions from 31 to 47 percent below baseline are
achieved. (Baseline refers to1those emission levels which are expected
to occur in the absence of additional control.) Furthermore, the technology
6-6
-------
can be extended to additional processing points (e.g., washing, drawing,
crimping, etc.) to arrive at a more stringent control level for these
facilities (referred to as Control Option B). An emission reduction
of 60 to 76 percent beyond the baseline emission rate is expected
using the extended control enclosure systems. Figures 6-2 and 6-3
present generalized schematics depicting these control options. In
addition to solvent recovery, the plant can also indirectly control
worker exposure t'o solvents and monomers with low threshold limit
values (TLV's). Capture systems are not expected to interfere with
the normal processing of the formed fiber or create any unusual operational
or safety problems.
A different approach which has the potential of achieving similar
levels of emission control (solvent recovery) has also been demonstrated
in the fibers industry. In short, the system uses a plant ventilation
or air management scheme in which air for the (post spinning) fiber
take-up room is taken from the dope preparation and fiber processing
areas. A fraction of the take-up room air is then used as spin cell
evaporation gas and is subsequently sent to solvent recovery (carbon
adsorption). Another fraction of the fiber take-up room air is used
to dilute the high concentration process gas sent to solvent recovery.
Since the level of control is dependent upon the amount of take-up
room air sent directly to carbon adsorption, it is possible to achieve
emission reductions similar to those involving the use of enclosures
through optimization of the volume of room air treated. The air
management system is used because the post spinning process steps for
this fiber type are somewhat unique. The technology is feasible
because the high Threshold Limit Value (TLV) for the solvent (acetone
at a TLV of 1,000 ppm) allows the vapor concentration in the fiber
extrusion (or take-up) room to reach a level that can be effectively
treated. Some producers also use this control system with a combination
of solvents. One solvent is used to produce one particular fiber type
and another solvent or combination of solvents is used to produce a
second fiber type within the same buildings. A mixture of volatilized
solvents is captured and sent to a single control or recovery device.
The individual solvents are then separated in the distillation stage.
The only operational criteria for use of the air management scheme are
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that each solvent be present at a concentration suitable for capture
and that individual solvent TLV'si are not exceeded. A significant
reduction in solvent TLV would likely restrict the use of this type of
control scheme; the alternative would be the use of an enclosed winding
or take-up area.
During the investigation of the synthetic fibers industry, it was
determined that within the acrylic fibers segment of the industry
there are manufacturing processes that do not involve the use of an
organic solvent. Although a viable control option for some plants,
this inorganic solvent production process was not considered applicable
to the entire fibers industry. There are no readily identifiable
inorganic solvent processes available for some acrylic or modacrylic
fibers; acrylic fibers manufactured using an organic solvent spinning
process cannot be reproduced exactly using inorganic processes. Also,
inorganic processes are available for other fiber types, such as
cellulose acetate.
There were also other reasons for eliminating its consideration
as a control option for the proposed standards. While the inorganic
process would result in an almost complete elimination of solvent VOC
emissions, it would also generate a significant water pollution problem.
Further, the inorganic solvent process (or portions of the process) is
under patent, and a number of complex legal and economic issues could
be raised if the proposed standards effectively forced a company to
use a specific process that may be owned and protected by a competitor.
The mutual competitive positions of the several acrylic fiber producers
would be substantially altered, and their customers (textile firms,
carpet manufacturers, etc.) would be forced to alter their processes
and products to accommodate whattwould in fact be different products.
The acrylic fibers produced using the large variety of processes have
certain specific but different characteristics that are well known and
expected by the purchasers for quality control reasons. For these
reasons, the inorganic solvent process is not considered a control
option available to all segments 1 of the synthetic fibers industry and
was not used as a basis for any regulatory alternative.
6-10
-------
Table 6-2 presents baseline emissions and summarizes the total
VOC emissions from each model plant. Also presented are the emission
rates and percent emission reduction associated with Control Options A
and B.
The baseline controlled model plants and Control Options A and B
provide the basis for three regulatory alternatives available to EPA
for regulation of VOC emissions from wet and dry solvent-spun fiber
plants. The three alternatives are based on emission control techniques
representative of three distinct levels of control. Table 6-3 summarizes
these alternatives and the control options available to the industry
to achieve each level.
Alternative I, referred to as baseline, is equivalent to no
additional regulatory action. For this alternative, VOC emission
levels would be the same as those currently achieved. It is important
to note that there are no State or local emission regulations which
apply specifically to the production of man-made fibers, nor is there
a Control Techniques Guideline (CTG) recommended emission limit. Of
the eight States containing fiber production facilities, most employ a
ceiling or guideline regulating VOC's which is similar to California's
Rule 66. Economic incentives rather than regulatory requirements,
however, dictate recovery of the solvents used in the processes.
Therefore, the VOC emission levels represented in Alternative I (with
the exception of Model Plant 2) reflect typical industry control
practices rather than levels imposed by regulations. Baseline control
for Model Plant 2 reflects expected or average control levels. A new
dry-spun acrylic manufacturing facility might not necessarily control
solvent VOC emissions to the extent now controlled by the only current
dry-spun acrylic manufacturer.
Alternative II is based on Control Option A and requires the use
of efficient vapor capture systems for process stages other than the
actual spinning step (i.e., spin cell exits and dryer exhausts) or .the
recirculation of a portion of room air to the process. Regulatory
Alternative III is based on Control Option B which extends the capture
and collection systems to additional processing points (e.g., washing,
drawing, crimping, heat setting, etc.) in the case of line enclosures
and to increased air volumes in the case of air management.
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6.3 ACRYLIC FIBER MODEL PLANTS: AND REGULATORY ALTERNATIVES30"40
Polyacrylonitrile resins used to make acrylic and modacrylic
fibers are produced by suspension or solution polymerization. Either
batch or continuous reaction modes may be employed, and either wet or
dry spinning may be used to form the fibers. In addition, a variety
of spinning solvents are used by industry. These include organic
solvents such as dimethylformamide (DMF), dimethylacetamide (DMAc) or
acetone and aqueous solutions of acids or salts such as zinc chloride
and sodium thiocyanate.
In an attempt to accurately represent the acrylic fibers industry
through definition of model plant parameters, three separate model
plants are presented. The three model plants are characterized according
to the process techniques presented in Table 6-4.
Table 6-4. ACRYLIC FIBER PROCESS TECHNIQUES
Model
Plant Polymerization
Number Medium
Polymerization
Operation
Spinning Spinning
Process Solvent
1
2
3
Suspension
or
Solution
Suspension
or
Solution
Suspension
Batch
or
Continuous
Batch
or
Continuous
Continuous
Wet
Dry
Dry
Organic
Organic
Organic
solvent,
solvent,
solvent,
DMAc
DMF
Acetone
6.3.1 Model Plant 1
6.3.1.1 Regulatory Alternative I, Baseline Control. This plant
is characterized by use of suspension or solution polymerization and
wet spinning with an organic solvent. The model plant block or schematic
diagram is presented in Figure 6-4; Table 6-5 presents tha relevant
model plant parameters. Major emission points, for wet spun acrylic
fibers, are the filtration, spihning, washing, drying, and crimping
steps where solvent is volatilized in room air. The diagram includes
identification of the major emission points which are normally vented
directly to the atmosphere. This plant represents the processes and
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Table 6-5. PARAMETERS FOR MODEL PLANT 1
General information ;
Type of Plant
Spinning Process
Polymerization Medium
Spinning Solvent
Production Capacity
Capacity Utilization ,
Raw Materials
Hours of Operation
Pollutants
Process Rates (Per 1,000 kg fiber)
Raw Materials In (PY)
Solvent Use (TS)
Polymer Fiber Produced (PS)
Residual Solvent in Fiber (RS)
Miscellaneous Non-Gaseous Solvent Loss
(Includes Distillation Loss)
Acrylic Fibers Plant
Wet Spinning
Suspension or solution
Dimethylacetamide (DMAc)
45.36 Gg/Year (100 MMPPY)
95 percent
Polyacrylonitrile, 98 percent
8,400 hours per year
DMAc
1,000 kg, PAN, 20 kg other materials
3,000 kg, DMAc
1,000 kg, Acrylic Fiber
5 kg, DMAc
25 kg, DMAc
Alternative I
Process Variables (Per 1.000 kg fiber) i (Baseline)
Make-up Solvent (MS)
70 kg
Alternative II
(Control Option A)
56 kg
Emission Sources (Per 1.000 kg fiber)
Filtering/Dissolving (El)
Spinning/Washing (E2)
Crimping/Drying (E3)
Cutting/Baling (E5)
Solvent Recovery Area (E4)
Miscellaneous Fugitives
Emission Totals
Alternative III
(Control Option B)
43 kg
1 kg
1 kg
1 kg
1 kg
4 kg
40 kg
26 kg
13 kg
Exhaust Gas Characteristics
Filtering/Dissolving (El)
Spinning/Hashing (E2)
Crimping/Drying (E3)
Cutting/Baling Area (E5)
Scrubber £1
Controlled Emission Source
Scrubber Type
Scrubber Efficiency
Feed Gas
Feed Gas Flow Rate
Feed Gas Solvent Concentration
Scrubbing Liquid Flow Rate
Residue Gas Solvent Concentration
Scrubber 12
Controlled Emission Source
Scrubber Type
Scrubber Efficiency
Feed Gas
Feed Gas Flow Rate
Feed Gas Solvent Concentration
Scrubbing Liquid Flow Rate
Residue Gas Solvent Concentration
Intermittent Flow: 140 M3/Min (5,000 ACFM)
Temperature: 27°C (80°F)
Solvent Concentration: 25 ppmv
Continuous Flow: 4,250 M3/Min (150,000 ACFM)
Temperature: 50°C (120°F)
Solvent Concentration: 100 ppmv
Continuous Flow: 1,700 M3/Min (60,000 ACFM)
Temperature: 82°C (180°F)
Solvent Concentration: 250 ppmv
Fugitives
Temperature: 27°C (80°F)
Solvent Concentration: 5 ppmv
Spinning/Washing
Bubble cap tower
98+ percent
Air/DMAc
570 M3/Min (20,000 ACFM)
650 ppm DMAc (1.2 kg/min)
500 kg/hr D.M. water
15 ppm (.02 kg/min)
Crimping/Drying
Bubble cap tower
98+ percent
Air/DMAc
1,700 M3/Min (60,000 CFM)
250 ppmv, DMAc (1.2 kg/min)
2,000 kg/hr, D.M. water
15 ppmv
6-16
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air pollution emission control technology currently in-use in this
particular segment of the acrylic fibers industry. This particular
production or process sequence is considered as "baseline control."
For a wet-spinning capacity of 45.36 Gg (100 MMPPY), it is assumed
that eight spin baths, each 3m x 5m, and eight washers, each 3m x 15m,
are needed together with appropriate fiber processing equipment to
complete the eight spinning lines. The process lines are essentially
open to room air. Ventilation hoods are located above the spinning
and washing areas and at various other major processing points. The
existing ventilation systems are designed around high air flow rates
with little emphasis on enclosures to reduce air volume flow.
6.3.1.2 Regulatory Alternative II, Control Option A. Since
major VOC emissions for this production sequence occur at spinning and
washing, an option for VOC emission control is to enclose these process
steps; the collected gases are then directed to a solvent recovery
scrubber. The enclosures would be reasonably tight i'n order to limit
the volume of gas to be treated. The enclosures would be sufficient
to cover the equipment, tied together with proper manifolding, and
equipped with doors at the correct spacing to permit operator access.
The enclosures would be tight enough to restrict the air flow to about
20,000 SCFM. If a flow of 20,000 SCFM is used, the VOC concentration
can be maintained well below the solvent lower explosive limit (1.8 percent
by volume). With a capture efficiency of 90 percent and a solvent
recovery (absorption/stripping) efficiency of 98 percent, the emission
reduction would amount to about 14 kg per 1,000 kg of polymer fiber.
Use of a solvent scrubber to treat gas streams from spinning, washing,
drawing, and drying would reduce VOC emissions and recover additional
spinning solvent. Figure 6-5 provides a schematic diagram of this
control option as applied to Model Plant 1. Table 6-5 contains the
model plant parameters for this option. Figure 6-6 shows the enclosures
in isometric and in plan and elevation views.
6.3.1.3 Regulatory Alternative III. Control Option B. This
control option incorporates the VOC control measures outlined in
Option A and includes the additional control of the emissions from the
filtering, crimping, and/or steam setting dryer. These processes,
which are normally vented directly to the atmosphere, would be collected,
and the exhaust gas stream would then be vented to a solvent recovery
6-17
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Figure 6-6. Ducts and Enclosures for
Acrylic Fibers Spinning and Washing Steps
6-19
-------
scrubber similar to the one described in Option A. The total gas
volume flow would be about 60,000 ACFM. Assuming a capture efficiency
of 90 percent and a control devijce efficiency of 98 percent, the
emissions reduction from baseline emissions resulting from Option B
would be about 27 kg per 1,000 kg of polymer fiber. Figure 6-7 presents
the model plant schematic for this process with Option B applied.
Details on the process parameters are contained in Table 6-5.
6.3.2 Model Plant 2
6.3.2.1 Regulatory Alternative I, Baseline Control. .This plant
is characterized by use of suspension or solution polymerization and
dry spinning with an organic solvent. The model plant block or schematic
diagram is presented in Figure 6-8; Table 6-6 presents the parameters
and technical details corresponding to the dry spinning model plant
schematic. For a dry spinning capacity of 45.36 Gg (100 MMPPY), four
spinning lines, each with 50 spinning cells per side, are needed
together with appropriate fiber processing equipment to complete the
model plant layout. This plant sequence represents "baseline control"
for the dry spinning of acrylic fibers.
6.3.2.2 Regulatory Alternative II, Control Option A. The spinning,
washing, steaming, and drying processes are the major VOC emission
sources in the dry spinning of acrylic fibers. Option A for this
process involves collecting the spinning emissions (solvent volatilized
as the fibers exit the spin cell and move to the processing stages)
with appropriate enclosures and venting the solvent containing gases
to a solvent recovery scrubber rather than to the atmosphere. If a
flow of 15,000 ACFM (spinning) is used for the gas stream, the solvent
concentration can be maintained well below the solvent lower explosive
limit (2.2 percent by volume). Assuming a capture efficiency of
90 percent and a recovery/control efficiency of 98 percent, the VOC
emission reduction would amount to about 14 kg of VOC per 1,000 kg of
polymer fiber produced from the spinning cell exits. Total solvent
recovered from Option A control would also be about 14 kg per 1,000 kg
of polymer. Figure 6-9 provides the schematic diagrams of this control
option as applied to Model Plant 2. Table 6-6 lists the appropriate
parameters for this control option in relation to the schematic diagrams.
6.3.2.3 Regulatory Alternative III, Control Option B. This
control option for the dry spinning of acrylics includes capture and
treatment of the steaming and,drying process steps exhaust gases as
6-20
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Table 6-6. PARAMETERS FOR MODEL PLANT 2
General Information
Type of Plant
Spinning Process
Polymerization Medium
Spinning Solvent
Production Capacity
Capacity Utilization
Raw Materials
Hours of Operation
Pollutants
Process Rates (Per 1,000 kg fiber)
Raw Materials In (PY)
Solvent Use (TS)
Polymer Fiber Produced (PS)
Residual Solvent in Fiber (RS)
Miscellaneous Non-Gaseous Solvent Loss
Acrylic Fibers Plant
Dry Spinning
Suspension or solution
Dimethylformamide (DMF)
45.36 Gg/Year (100 MMPPY)
95 percent
Polyacrylonitrile, 98%, 2% other material
8,400 hours per year
DMF
1,000 kg, PAN, 20 kg other materials
2,200 kg, DMF
1,000 kg, Acrylic Fiber
5 kg, DMF
20 kg, DMF
Alternative I Alternative II Alternative III
Process Variables (Per 1.000 kg fiber) (Baseline)(Control Option A) (Control Option B)
Make-up Solvent (MS) 70 kg 56 kg 42 kg
Emission Sources (Per 1,000 kg fiber) . •
Filtering/Dissolving (El) ,1kg
Spin Cell Exits (E4) 15 kg
Wash/Draw/Crimp (E2) 2 kg
Piddle/Waste System (E5) 6 kg
Steaming/Drying (E3) . 15 kg
Solvent Recovery Area 1 kg
Miscellaneous Fugitives 5 kg
Emission Totals 45 kg
kg
kg,
kg
kg
15 kg
31 kg
kg
kg
kg
kg
1 kg
2 kg
5 kg
18 kg
Exhaust Gas Characteristics
Filtering/Dissolving (El)
Spin Cell Exits (E4)
Steaming/Drying (E3)
Hash/Draw/Crimp (E2)
Scrubber #1
Controlled Emission Source
Scrubber Type
Scrubber Efficiency
Feed Gas
Feed Gas Flow Rate
Feed Gas Solvent Concentration
Scrubbing Liquid Flow Rate
Residue Gas Solvent Concentration
Scrubber #2
Controlled Emission Source
Scrubber Type
Scrubber Efficiency
Feed Gas
Feed Gas Flow Rate
Feed Gas Solvent Concentration
Scrubbing Liquid Flow Rate
Residue Gas Solvent Concentration
Intermittent Flow: 140 M3/Min (5,000 ACFM)
Temperature:- 38°C (100°F)
Solvent Concentration: 10 ppmv
Continuous Flow: fugitive emissions
Temperature: 38°C (100°F)
Solvent Concentration: Variable
Continuous Flow: 1,700 M3/Min (60,000 ACFM)
Temperature: 82°C (180°F)
Solvent Concentration: 300 ppmv
Continuous Flow: 5,700 M3/Min (200,000 ACFM)
Temperature: 38°C (100°F)
Solvent Concentration: 10 ppmv
Spinning (E4)
Bubble cap tower
98+ percent
Air/DMF
425 M3/Min (15,000 ACFM)
1,000 ppm DMF (1.3 kg/min)
400 kg/hr D.M. water
20 ppm (.03 kg/min) DMF
Streaming/Drying (E3)
Bubble cap tower
98+ percent
Air/DMF
1,700 M3/Min (60,000 CFM)
300 ppmv, DMF (1.28 kg/min-)
2,000 'kg/hr, D.M. water
10 ppmv DMF (0.02 kg/min)
6-23
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well as those from the spinning cell exit. The total exhaust gas
stream from the steaming and drying stages would be vented to a solvent
recovery scrubber similar to the one described in Option A. The
enclosures on these process stages would be reasonably tight in order
to limit the fugitive losses. If a flow of 60,000 CFM is used to
characterize the combined exhaust gas stream, solvent concentrations
are maintained well below the lower explosive limit (2.2 percent by
volume). The dryer air flow rate is related directly to product
quality control and, as a process variable, cannot be reduced to
increase the solvent concentration. Assuming a capture efficiency of
about 90 percent at the steaming/drying stage and a control device
efficiency of 98 percent, the total VOC emission reduction measured
from baseline control resulting from application of Option B controls
would be about 27 kg of VOC per 1,000 kg of fiber. Figure 6-10 presents
the model plant schematic for this model plant with Option B applied.
Details on the process parameters are contained in Table 6-6.
6.3.3 Model Plant 341"50
6.3.3.1 Regulatory Alternative I, Baseline Control. This model
plant is based on suspension polymerization and dry spinning with
acetone as the organic solvent. The processing or manufacturing
stages are quite similar to those of the preceding model plants.
Polymer (or copolymers) is dissolved in solvent, blended, filtered,
dry spun, drawn, washed, crimped, and dried. For this segment of the
acrylic fiber industry, a model plant capacity of 20 Gg per year
(44 MMPPY) was selected. For this dry spinning capacity, two spinning
lines, each with 50 spinning cells per side, are required as well as
the appropriate downstream fiber processing equipment.
The major emissions from this dry spinning process are volatilized
solvent losses which occur at a number of points in the overall pro-
duction scheme. Solvent emissions occur during dissolving of the
polymer, blending of the spinning solution, filtering of the dope,
spinning of the fiber, treating of the fiber after spinning, and
during the solvent recovery process. Figure 6-11 presents a process
flow diagram, with emission points shown, for this segment of the
acrylic fibers industry. Table 6-7 includes the model plant param-
eters relevant to the diagram. This production or process sequence is
considered as "baseline control" for this model plant.
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Table 6-7. PARAMETERS FOR MODEL PLANT 3
General Information
Type of Plant
Spinning Process
Polymerization Medium
Spinning Solvent
Production Capacity
Capacity Utilization
Raw Materials
Hours of Operation
Pollutants
Process Rates (Per 1.000 kg fiber)
Raw Materials In (PY)
Solvent Use (TS)
Polymer Fiber Produced (PS)
Residual Solvent in Fiber (RS)
Miscellaneous Solvent Loss
Modacrylic Fibers Plant
Dry Spinning
Suspension
Acetone
20 Gg/Year (44 MMPPY)
95 percent
Polyacrylonitrile and Vinylidene Chloride,
98 percent, 2% other material
8,400 hours per year
Acetone
1,000 kg, Polymer/copolymer,
20 kg other materials
2,500 kg, Acetone
1,000 kg, Modacrylic Fiber
5 kg, Acetone
10 kg, Acetone
Alternative I
Process Variables (Per 1,000 kg fiber) :
Make-up Solvent (MS)
Emission Sources (Per 1,000 kq fiber)
Filtering/Dissolving (El)
Spinning/Washing/Cr imping (E2)
Drying (E3)
Solvent Recovery Area (E4)
Spinning Scrubber
Emission Totals
Alternative II
(Baseline) (Control Option A)
155 kg 101 kg
5 kg 5 kg
57 kg 57 kg
55 kg 1 kg
23 kg 23 kg
140 kg
86 kg
Alternative III
(Control Option B)
48 kg
5 kg
3 kg
•1 kg
23 kg
JJa
33 kg
Exhaust Gas Characteristics
Filtering/Dissolving (El)
Spinning/Washing/Crimping (E2)
Drying (E3)
ScrubberII
Controlled Emission Source
Scrubber Type
Scrubber Efficiency
Feed Gas
Feed Gas Flow Rate
Feed Gas Solvent Concentration
Scrubbing,Liquid Flow Rate
Residue Gas Solvent Concentration
Scrubber $2
Controlled Emission Source
Scrubber Type
Scrubber Efficiency
Feed Gas
Feed Gas Flow Rate
Feed Gas Solvent Concentration
Scrubbing Liquid Flow Rate
Residue Gas Solvent Concentration
Intermittent Flow: 140 M3/Min (5,000 ACFM)
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
Continuous Flow: Fugitive Emissions
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
Continuous Flow: 425 M3/Min (15,000 ACFM)
Temperature: 60°C (140°F)
Solvent Concentration: 2,300 ppmv
Dryer (E3)
Bubble cap tower
98+ percent
Air/Acetone
425 M3/min (15,000 ACFM)
2,300 ppmv (2.0 kg/min), Acetone
600 kg/hr D.M. water
40 ppm (.04 kg/min), Acetone
Spinning/Washing (E2)
Bubble cap tower
98+ percent
Air/Acetone
425 M3/Min (15,000 CFM)
2,300 ppmv (2.0 kg/min) Acetone
600 kg/hr, D.M. water
40 ppmv (0.04 kg/min), Acetone
6-28
-------
6.3.3.2 Regulatory Alternative II. Control Option A. The major
VOC emissions from this fiber production process occur at the spinning
cell fiber exit, during drawing and washing of the spun fibers, and
during drying of the fiber tow. Option A for this production sequence
involves the collection of the exhaust gases from the fiber dryer
(which contain significant amounts of volatilized solvent) and treatment
of these gases in a solvent recovery system. The solvent recovery
system may consist of either a solvent scrubber or a carbon adsorption
system. For the purpose of the model plant analysis, it is assumed
that a scrubber is used. Assuming a solvent recovery efficiency of
98 percent, the emission reduction would amount to about 54 kg solvent
per 1,000 kg of polymer processed. Capture efficiency at drying is
nearly 100 percent, since 100 percent of the dryer exhausts are routed
to the control device. Figure 6-12 shows the schematic diagram of
this control option as applied to Model Plant 3; Table 6-7 contains
the model plant parameters for this option.
6.3.3.3 Regulatory Alternative III. Control Option B. The major
VOC emissions from this fiber production process occur at the spinning
cell fiber exit, during drawing and washing of the spun fibers, and
during drying of the fiber tow. Option B for this production sequence
would require enclosure of the post spinning processing stages with
the collected gases sent to a solvent recovery scrubber or carbon bed;
a scrubber is specified for the model plant analysis. The exhaust
gases from the fiber dryer would also be treated in a solvent recovery
system. The process enclosures would be tight enough to limit the
volume of gas to be treated to about 15,000 ACFM (not including dryer
exhaust). At this flow rate, the VOC concentration can be maintained
well below the lower explosive limit (2.6 percent by volume). Capture
efficiency at post spinning processing stages would be 90 percent.
Dryer emissions would be 100 percent captured. Assuming a control
device efficiency of 98 percent (after capture), the VOC emission
reduction from baseline control will amount to about 54 kg per 1,000 kg
polymer fiber from the dryer and about 53 kg per 1,000 kg of polymer
fiber from the spinning, drawing, and washing stages. Figure 6-13
shows the schematic diagram of this control option as applied to Model
Plant 3; Table 6-7 contains the model plant parameters for this option.
6-29
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6.4 CELLULOSE ACETATE FIBER MODEL PLANTS AND REGULATORY ALTERNATIVES51"68
In order to characterize the plants utilized in production of
[
cellulose acetate fibers, two|basic model plants were selected. One
represents the cigarette filtration tow segment of the cellulose
acetate industry, and the second represents the textile fibers segment.
For both segments of the industry, the polymer dissolving and spinning
portions of the model plants are identical; the major difference in
the two fiber processes is in the post spinning process segments.
For the cellulose acetate fiber industry, a model plant capacity of
I
22.7 Gg (50 MMPPY) per year was selected. The polymer consists of
100 percent cellulose acetate; both model plants use acetone as the
solvent. For a capacity of 22.7 Gg (50 MMPPY), it is assumed that
four spinning lines, each with 50 spinning cells per side, are required
along with the appropriate post spinning fiber processing equipment to
complete the model plants.
6.4.1 Model Plant 4
6.4.1.1 Regulatory Alternative I. Baseline Control. This model
plant represents the production sequence utilized in the manufacture
of cellulose acetate cigarette filtration tow. Dried acetate flakes
are dissolved in a solvent, blended, filtered, and sent to the spinning
machines. The post spinning treatment of filter tow fibers includes
finish application, crimping,|and drying. The post spinning fiber
processing steps are typically open to room air; the exception being
the dryer which is normally controlled. Since the fibers emerging
from the spin cells contain as much as 15 to 20 percent residual
solvent, significant amounts of solvent are volatilized into the room
air. Figure 6-14 presents the model plant schematic diagram, and
Table 6-8 contains the relevant model plant parameters for this segment
of the industry. This model plant represents the processes and (solvent
recovery) air pollution control technology currently in use in this
particular segment of the cellulose acetate fibers industry. This
production or process sequence is considered as "baseline control."
6.4.1.2 Regulatory Alternative II, Control Option A. The major
emissions from the manufacture of cigarette filtration tow occur in
the post spinning fiber processing stages. Residual solvent in the
6-32
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6-33
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Table 6-8. PARAMETERS FOR MODEL PLANT 4
General Information
Type of Plant
Spinning Process
Polymerization Medium
Spinning Solvent
Production Capacity
Capacity Utilization
Raw Materials
Hours of Operation
Pollutants
Process Rates (Per 1,000 kg fiber)
Raw Materials In (PY)
Solvent Use (TS)
Polymer Fiber Produced (PS)
Residual 'Solvent in F'iber (RS)
Miscellaneous"Solvent Loss (ML)
Cellulose Acetate Filtration Tow Plant
Dry Spinning
Solution
Acetone
22.7 Gg/Year (50 MMPPY)
95 percent
Cellulose Acetate, 98%, 2% other material
8,400 hours per year
Acetone
1,000 kg, Cellulose Acetate,
20 kg other materials
3,000 kg, Acetone
1,000 kg, Acetate Filter Tow
Negligible
10 kg Acetone
Alternative I Alternative II Alternative III
Process Variables (Per 1,000 kg fiber) (Baseline) (Control Option A) (Control Option B)
Make-up Solvent (MS) 130 kg 77 kg 54 kg
Emission Sources (Per 1,000 ka fiber)
Filtering/Dissolving (El)
Spinning/Finishing (E2)
Crimping (E3)
Solvent Recovery Area
Dryer Carbon Bed Exhausts (E4)
Spin Enclosure Carbon Bed
Exhausts
Emission Totals
2 kg
60 kg
25 kg
28 kg
5 kg
> 120 kg
2 kg
6 kg
25 kg
28 kg
5 kg
1 kg
6/ kg
2 kg
6 kg
2 kg
28 kg
5 kg
1 kq
44 kg
Exhaust Gas Characteristics
Filtering/Dissolving (El)
Spinning/Finishing (E2)
Crimping (E3)
Carbon Adsorber #1
Controlled Emission Source
Adsorber Type
Adsorption Efficiency
Feed Gas
Feed Gas-Flow Rate
Feed Gas Solvent Concentration
Residue Gas Solvent Concentration
Carbon Adsorber iZ
Controlled Emission Source
Adsorber Type
Adsorption Efficiency
Feed Gas
Feed Gas Flow Rate
Feed Gas Solvent Concentration
Residue Gas Solvent Concentration
Intermittent Flow: 140 M3/Min (5,000 ACFM)
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv in room air
Continuous Flow: Fugitives
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv in room air
Continuous Flow: Fugitives
Temperature: 50°C (120°F)
Solvent Concentration: 1,000 ppmv in room air
Spinning/Finishing (E2)
Fixed Bed w/steam regeneration
98+ percent
Air/Acetone
425 M3/Mih (15,000 ACFM)
2,500 ppmv (2.5 kg/Min), Acetone
50 ppm
Spinning/Finishing/Crimping
Fixed Bed w/steam, regeneration
98+ percent
Air/Acetone
570 M3/Min (20,000 CFM)
2,650 ppmv, (3.5 kg/min), Acetone
50 ppmv
6-34
-------
fiber is volatilized into the room or building air which is then
vented to the atmosphere. Option A for this production process would
require the treatment of all dryer exhaust gases for solvent recovery
and the enclosure of the spin cell exits and the tow line up to the
crimping stage. The captured gases containing solvent vapor would be
vented directly to a solvent recovery system. The solvent recovery
system may consist of either a solvent scrubber or a carbon adsorption
system. For analysis of this model plant case, it is assumed that a
carbon adsorption system is used to recover the solvent; carbon adsorption
systans are in use at nearly all cellulose acetate fiber plants for
solvent recovery.
Assuming a 90 percent capture efficiency and a 98 percent solvent
recovery efficiency for the spin cell enclosures and solvent recovery
system, respectively, the VOC emission reduction would be about 53 kg
solvent per 1,000 kg of polymer fiber processed. Figure 6-15 provides
a schematic diagram of this control option as applied to Model Plant 4.
Table 6-3 lists the model plant parameters corresponding to the
figure. The carbon adsorption system used to recover solvent from the
spin cell enclosures involves fixed bed adsorption with steam
regeneration. The system includes carbon beds, blowers, condensers,
piping, valves, and instrumentation.
6.4.1.3 Regulatory Alternative III, Control Option B. Option B
for the control of VOC emissions from the manufacture of cigarette
filtration tow requires, in addition to the treatment of all dryer
exhaust gases, the use of process enclosures for control of fugitive
emissions at all the post spinning fiber processing stages where
residual solvent is volatilized into room air, including the crimping
stage. Enclosures can be placed at the exit of the spinning cells and
along the fiber processing line, up to the fiber dryer. The collected
gases are then directed to a solvent recovery system. The enclosures
would be sufficient to cover the equipment, tied together with proper
manifolding, and equipped with doors at the correct spacing to permit
operator access. The enclosures would be tight enough to restrict the
air flow to about 20,000 ACFM. If a flow of 20,000 ACFM is used, the
solvent (VOC) concentration can be maintained well below the solvent
6-35
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lower explosive limit (2.6 percent by volume). The solvent recovery
system may consist of either a solvent scrubber or a carbon adsorption
system. For the purpose of the model plant analysis, it is assumed
that a carbon adsorption system is used since these solvent recovery
systems are in use at nearly all cellulose acetate fiber plants.
Assuming a 90 percent capture efficiency and a 98 percent solvent
recovery efficiency, the VOC emission reduction from baseline control
will amount to about 76 kg of VOC per 1,000 kg of polymer processed.
Figure 6-16 provides a schematic diagram of this control option as
applied to Model Plant 4. Table 6-3 lists the model plant parameters
corresponding, to the figure. The carbon adsorption system involves
fixed bed adsorption with steam regeneration. The system includes
carbon beds, blowers, condensers, condensate decanter, piping, valves,
and instrumentation.
6.4.2 Model Plant 5
6.4.2.1 Regulatory Alternative I. Baseline Control. The cellulose
acetate textile yarn process is represented in this model plant. The
process stages prior to fiber exit from the spinning cell are identical
to those of acetate filtration tow. Dried acetate flakes are dissolved
in a solvent, blended, filtered, and sent to the spinning machines.
Immediately after spinning, acetate textile yarn is wound onto a
bobbin as continuous filament yarn, with no further treatment. The
yarn is later transferred to larger spools for shipment or further
processing in another part of the plant. As the fibers are initially
wound onto bobbins, they may still contain as much as 15 to 20 percent
residual solvent. This residual solvent continuously evaporates into
room or building air until equilibrium is reached in the fiber at
around 1 or 2 percent (by weight) residual solvent. These fugitive
emissions are about 145 kg VOC per 1,000 kg of polymer processed on an
industry-wide basis. Figure 6-17 presents the model plant schematic
diagram, and Table 6-9 contains the relevant model plant parameters
for the production sequence considered as baseline control.
6.4.2.2 Regulatory Alternative II, Control Option A. This
control alternative involves the use of a gross in-plant air management
scheme to achieve optimum solvent recovery. The air management system
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6-39
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Table 6-9. PARAMETERS FOR MODEL PLANT 5
General Information
Type of Plant
Spinning Process
Polymerization Medium
Spinning Solvent
Production Capacity
Capacity Utilization
Raw Materials
Hours of Operation
Pollutants
Process Rates (Per 1.000 kg fiber) ;
Raw Materials In (PY) •
Solvent Use (TS)
Polymer Fiber Produced (PS)
Residual Solvent in Fiber (RS)
Miscellaneous Non-Gaseous Solvent Loss
Total Solvent Evaporated to
Room Air
Yarn
Cellulose Acetate Textile
Dry Spinning
Solution
Acetone
22.7 Gg/Year (50 MMPPY)
95 percent
Cellulose Acetate 98 percent,
2 percent other materials
8,400 hours per year
Acetone
1,000 kg, Acetate, 20 kg other materials
3,000 kg, Acetone
1,000 kg, Acetate Textile Yarn
10 kg, Acetone
20 kg, Acetone
122 kg, Acetone
Process Variables (Per 1.000 kg fiber) • (Baseline)
Alternative I Alternative II
Alternative III
Make-up Solvent (MS)
Emission Sources (Per 1.000 kg fiber)
175 kg
(Control Option' A) (Control Option B)
96 kg 70 kg
Filtering/Dissolving (El)
Spinning/Winding (E2) (E3)
Solvent Recovery Area
Miscellaneous Fugitives
Emission Totals
5 kg
105 kg .
30 kg
5 kg
145 kg
1 kg
30 kg
30 kg
_Oa
66 kg
1 kg
4 kg
30 kg
_5_Jkg
40 kg
Exhaust Gas Characteristics
Filtering/Dissolving (El)
Spinning/Winding (E2) (E3)
Total Air to Extrusion Room
From Filtering/Winding
Room Air Used as Process Air
in Alternatives II and III
Room Air Lost as Fugitives
(El, E2, E3, and Misc.)
Room Air Sent Directly to
Recovery
Intermittent Flow: Fugitive Losses
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
Continuous Flow: Fugitive Losses
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
Continuous Flow: 3,500 M3/Min (125,000 ACFM)
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
Continuous Flow: 3,500 M3/Min (125,000 ACFM)
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
Continuous Flow: 700 M3/Min (25,000 ACFM)
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
Continuous Flow: 1,400 M3/Min (50,000 ACFM)
Temperature: 27°C (80°F)
Solvent Concentration: 1,000 ppmv
6-40
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requires the re-use of plant air from the three basic process areas of
the fiber plant. Room air from the dope preparation area (dissolving,
mixing, filtering) and room air from the twisting/coning/beaming
areas, both of which contain low levels of solvent, are vented
(transported) to the extrusion room at a predetermined flow rate. The
extrusion room air can then be used to supply the process or evaporation
air for the spinning-cell solvent evaporation system. The solvent-rich
process air, together with a fixed amount of solvent-lean extrusion
room air, is then vented directly to a solvent recovery system. The
ratio of process air to (direct) room air may vary somewhat depending
on the individual plant. To properly accomplish the air management
program, the plants would likely maintain a slight negative room
pressure of about 0.1 to 0.2 inches of water.
For a cellulose acetate textile yarn plant capacity of 22.7 Gg/year
(50 MMPPY), a total of about 125,000 CFM would be sent to the solvent
recovery system. Of this amount, about 125,000 CFM, nearly all the
gas would be from the spinning cells; little or no air would be taken
directly from the extrusion room. Figure 6-18 and Table 6-9 present
the relevant model plant parameters for this option. Since this model
plant represents that segment of the cellulose acetate fiber industry
which produces textile filament yarn, consideration has been given to
the fact that a plant of this type might utilize more than one solvent
in the production of acetate fibers. Solvent-laden air streams would
therefore contain two or more VOC's, and carbon adsorption efficiency
of any given system will tend to be lower on a multiple organic feed
versus a single organic (see Chapter 4 for discussion). To account
for this, a lower overall recovery efficiency is assigned to this
model plant control scheme, 95 percent as opposed to 98 percent.
Assuming a 95 percent solvent recovery efficiency from the control
device, the VOC emission reduction would amount to about 79 kg of VOC
per 1,000 kg of polymer processed. The solvent recovery system may
consist of either a solvent scrubber or a carbon adsorption system.
For the purpose of the model plant analysis, it is assumed that a
carbon adsorption system is used. The carbon adsorption system involves
fixed bed adsorption with steam regeneration. The system includes
6-41
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carbon beds, blowers, condensers, piping, valves, and instrumentation.
Design parameters include operating capacity, carbon requirements,
flow rates, temperatures, bed depth, pressure drop, loading time, bed
area, cycle time, and regeneration requirements.
6.4.2.3 Regulatory Alternative III. Control Option B. The
control alternative involves use of the same in-plant air management
scheme described in Option A. The difference is that this Option
calls for the treatment of an additional 50,000 ACFM of extrusion room
air. A total of about 175,000 CFM would be sent to the solvent recovery
system. Of this amount 125,000 CFM would be from the spinning cells,
and 50,000 CFM would be taken directly from the extrusion room.
Extrusion room make-up air of 50,000 CFM would be drawn from the
pre-spinning and post-spinning process areas. A bypass system is
necessary to ensure the room air concentration does not exceed 1,000 pprn.
This control option would also require measures to adequately control
the loss of extrusion room air to the atmosphere from the building
door, windows, etc. A negative pressure of about 0.1 to 0.2 inches of
water would likely be maintained in the buildings to prevent losses.
Total solvent loss as fugitives in room air would then amount to about
13 kg of solvent per 1,000 kg of polymer. Figure 6-18 and Table 6-9
present the relevant model plant parameters for this option. Assuming
a 95 percent solvent recovery efficiency from the carbon beds, the VOC
emission reduction will amount to about 105 kg per 1,000 kg of polymer.
6-43
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6.5 REFERENCES
3.
4.
5.
6.
7.
8.
9.
10,
11.
Chemical Economics Handbook. Stanford Research Institute. Menlo
Park, California. March 1978. Fibers-540.000.
Parr, J.L. Industrial Process Profiles for Environmental Use.
U.S. Environmental Protection Agency. November 1976. Chapter 11 - The
Synthetic Fibers Industry.
Moncrief, R.W. Man-Made Fibers. London, Boston. Nevves-Sutterworths.
1975.
Click, C.N. and Moore, D.O. Emission, Process and Control Technology
Study of the ABS/SAN, Acrylic Fiber, and NBR Industries. Pullman-Kailogg,
Inc. Houston, Texas. Report to EPA, Contract No. 68-02--2619,
Task No. 6. April 1979.
Welfers, Dr. E. Process and Machine Technology of Man-Made Fiber
Production. International Textile Bulletin. (Schlieren/Zurich.)
World Spinning Edition: 174-204. February, 1978.
Zerbonia, R. and Lathan, G. Phase I Source Category Survey Report.
Prepared for the Office of Air Quality Planning and Standards,
U.S. Environmental Protection Agency, during development of New
Source Performance Standards for the synthetic fibers industry.
Pacific Environmental Services, Inc. Research Triangle Park,
North Carolina. February 14, 1980.
Report of the Initial Plant Visit to DuPont Corporation Waynesboro
Plant, Waynesboro, Virginia. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. May 1, 1980.
Correspondence from Mullen, T.W. Jr., DuPont (Waynesboro Plant)
to Manley, R., Pacific Environmental Services, Inc. June 9,
1981. Subject spandex process information.
Report of the Plant Visit !to Globe Manufacturing Company, Gastonia,
S.C. U.S. Environmental Protection Agency Office of Air Quality
Planning and Standards, Research Triangle Park, N.C. December 1,
1981.
Correspondence from Legendre, R., Globe Manufacturing Company to
Crumpler, D.C., U.S. Environmental Protection Agency. June 26,
1980. Patent and process information.
Report of November 12, 1981 meeting between representatives of
Globe Manufacturing Company and EPA in Durham, N.C. Subject
solvent recovery and costs. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. December 2, 1981.
6-44
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12. Trip Report. Plant Visit to Globe Manufacturing Company, Gastonia,
North Carolina. September 16-17, 1981.
13. Memorandum and attachments from Zerbonia, R.A., Pacific Environmental
Services, Incorporated, to Docket No. A-80-7. November 10, 1981.
Control Costs and Regulatory Alternative Development for Reaction
Spun Spandex Fiber Process (Carbon Adsorption vs. Incineration).
14. Welfers, E. Process and Machine Technology of Man-made Fiber
Production. International Textile Bulletin. World Edition.
February 1978. pp. 153-262.
15. Air Pollution Engineering Manual. Air Pollution Control District
County of Los Angeles. U.S. Environmental Protection Agency.
Research Triangle Park, N.C. Publication No. AP-40. May 1973.
pp. 207-229.
16. Radian Corporation. Control Techniques for Volatile Organic
Emissions from Stationary Sources. U.S. Environmental Protection
Agency. Research Triangle Park, N.C. Publication No. EPA-450/2-78-022.
May 1978. pp. 70-83. .
17. Control Techniques for Hydrocarbon and Organic-Solvent Emissions
from Stationary Sources. U.S. Public Health Service. Washington,
D.C-. Publication No. AP-68. March 1970. p. 114.
18. VIC Manufacturing Company. Carbon Adsorption/Emission Control -
Benefits and Limitations. Minneapolis, Minnesota, pp. 7-8.
19. McCabe, W.L.'and Smith, J.C. Unit Operations of Chemical Engineering,
Second Edition. McGraw-Hill Book Company. 1967. pp. 517-539.
20. Peters, M.S. and Timmerhaus, K.D. Plant Design and Economics for
Chemical Engineers. McGraw-Hill Book Company, Second Edition.
1968. pp. 614-655.
fj
21. Perry, R.H. et al., Section 14: Gas Absorption and Solvent
Extraction. Chemical Engineer's Handbook. McGraw-Hill Book
Company, Fourth Edition. 1963. p. 14-24 through 14-34, and
p. 18-1 through 18-25.
22. Calvert, J. et al. "Wet Scrubber System Study" Volume I. Scrubber
Handbook. APT, Incorporated. EPA R2-72-118A, CPA 70-95. July 1972.
23. Letter and attachments from Massey, N.A., Process Simulation
Consultant, AAA Technology and Specialties Company Incorporated,
to Zerbonia, R.A., PES, Incorporated. October 1, 1980. Computer
Runs to Simulate the Absorber/Stripper Columns.
24. Telecon. Bjorness, R.A., Metex Process Equipment Corporation,
with Berard, R.E., PES, Incorporated. September 15, 1980. Cost
data for binary absorption columns of varying parameters.
6-45
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25.
26.
27.
28.
Cheremisinoff, P.N. and Ellerbusch, Fred. Carbon Adsorption
Handbook. Ann Arbor Science Publishers, Incorporated. 1978.
McDennott, H.J. Handbook !of Ventilation for Contaminant Control
Ann Arbor Science Publishers, Incorporated. 1976. p. 101-185.
Industrial Ventilation-A Manual of Recommended Practice.
Conference of Governmental Industrial Hygienists. 1980.
American
Click, C.N. and Moore, D.O. Emission, Process, and Control Technology
Study of the ABS/SAN, Acrylic Fiber, -and NBR Industries; Pullman-Kellogg.
(Report to EPA, Contract rjo. 68-02-2619, Task No. 6). April 1979.
Appendix D.
29. Economic Impact Assessment for Acrylonitrile. Enviro Control,
Incorporated. (Report tojOSHA, Contract No. J-9-F-6-0229, Task 3).
February 21, 1978.
30. Report of the Initial Plant Visit to American Cyanamid Company
Santa Rosa Plant, Milton,'Florida. Prepared for the Office of
Air Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. April 11, 1980.
31. Report of the Plant Visitjto Badishe Corporation Synthetic Fibers
Plant, Williamsburg, Virginia. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. November 28, 1979.
32. Reference 7, p. 1.
33. Report of the Initial Plant Visit to DuPont Corporation May
Plant, Camden, South Carolina. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. April 29, 1980.
34. Report of the Initial Plant Visit to Monsanto Company acrylic
fiber plant, Decatur, Alabama. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. April 1, 1980.
35. Reference 8, pp. 3, 7.
6-46
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36. Report of January 27, 1982, plant visit to DuPont Company May
Plant, Camden, S.C. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. March 2, 1982.
37. Synthetic Fibers Industry, Emission Test Report Monsanto Textiles
Company, Decatur, Alabama. U.S. Environmental Protection Agency,
OAQPS. Research Triangle Park, N.C. EMB Report 80-SNF-2.
February 1981.
38. Synthetic Fibers Industry, Emission Test Report El du Pont de Nemours
and Company May Plant, Camden, South Carolina. EMB Report 80-SNF-l.
U.S. Environmental Protection Agency. February 1981.
39. Statement from Earnhart, C.R., DuPont Company, to National Air
Pollution-Control Techniques Advisory Committee. September 22,
1981. Proposed NSPS for synthetic fibers production' facilities.
40. Report of meeting with Earnhart, C.R., DuPont Company, and EPA/PES
synthetic fibers NSPS project team. November 1981. Technical
and economic issues.
41. Report of Initial Plant Visit to Tennessee Eastman Company,
Kingsport, Tennessee. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. December 13, 1979.
42. Report of Meeting between Tennessee Eastman Company representatives
and EPA in Durham, N.C. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic,fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. October 28, 1981.
43. Volatile Organic Compound Emission Inventory for Tennessee Eastman
Company. U.S. Environmental Agency Region IV. Atlanta, Georgia.
EPA 904/9-78-023. December 1978.
44. Correspondence from Edwards, J.C., Tennessee Eastman Company to
Manley, R., Pacific Environmental Services, Inc. December 2,
1981. Subject process information.
45. Report of November 10, 1981 meeting between representatives of
Tennessee Eastman Company and EPA in Durham, N.C. Prepared for
the Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, during development of New Source Performance
Standards for the synthetic fibers industry. Pacific Environmental
Services, Inc. Research Triangle Park, North Carolina. December 21,
1981.
6-47
-------
46. Report of September 30, 1981 plant visit to Tennessee Eastman
Company, Kingsport, Tennessee. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers ;industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. October 1981.
47. Report of January 2, 1982, plant visit to Tennessee Eastman Company,
Kingsport, Tennessee. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. March 2, 1982.
48. Report of the Initial Plant Visit to Tennessee Eastman Company
Synthetic Fibers Manufacturing Facility in Kingsport, Tennessee.
Prepared during Development of New Source Performance Standards
for the synthetic fibers industry. December 13, 1979.
49. Statement from Ritchie, Tom, Tennessee Eastman Company, to National
Air Pollution Control Techniques Advisory Committee. September 22,
1981. Proposed NSPS for synthetic fibers production facilities.
50. Report of meeting with Vaughn McCoy, et al., Tennessee Eastman
Company, and EPA/PES synthetic fibers NSPS project team,, December 1,
1981. Technical and economic issues.
51. Reports of the Phase II Plant Visit to Celanese Fibers Company
Celriver acetate plant, Narrows, Virginia. Prepared for the
Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, during development of New Source Performance
Standards for the synthetic fibers industry. Pacific Environmental
Services, Inc. Research Triangle Park, North Carolina. May 28,
1930.
52. Report of Phase II Plant Visit to Celanese Fibers Company Celco
acetate plant, Rock Hill, South Carolina. Prepared for the
Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, during development of New Source Performance
Standards for the synthetic fibers industry. Pacific Environmental
Services, Inc. Research Triangle Park, North Carolina. August 11,
1980.
53. Reference 41, p. 1.
54. Reference 42, p. 2. .
55. Reference 43, p. 2-1.
56. Reference 44, p.l.
57. Reference 45, p. 1.
58. Reference 46, pp. 1, 2.
6-48
-------
59. Reference 47, p. 1.
60. Report of the August 11, 1980, plant visit to Celanese Fibers
Company Celco plant, Narrows, Virginia. Prepared for the Office
of Air Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. September 1980.
61. Letter and attachments from Pullen, J.C., Celanese Fibers Company,
to Zerbonia, R.A., Pacific Environmental Services, Incorporated.
July 3, 1980. Response to Section 114 information request (Celco
Acetate Fiber Plant, Narrows, Virginia).
62. Report of the Phase II Plant Visit to Celanese Fibers Company
Celriyer Acetate Plant in Rock Hill, South Carolina. Prepared
during the Development of New Source Performance Standards for
the synthetic fibers industry. May 28, 1980.
63. Letter and attachments from Pullen, J.C., Celanese Fibers Company,
to Zerbonia, R.A., Pacific Environmental Services, Incorporated.
July 3, 1980. Response to Section 114 information request (Celriver
Acetate Fiber Plant, Rock Hill, South Carolina).
64. Letter from Pullen, J.C., Celanese Fibers Company, to National
Air Pollution Control Techniques Advisory Committee. September 8,
1981. Proposed NSPS for synthetic fiber production facilities.
65. Report of meeting with Pullen, J.C., Celanese Fibers Company, and
EPA/PES synthetic fibers NSPS project team. December 3, 1981.
Technical and economic issues.
66. Reference 49, pp. 11-43, 44, 47, 48.
67. Reference 50, pp. 1,2.
68. Letter and attachments from Pullen, J.C., Celanese Fibers Company,
to Manley, R., Pacific Environmental Services, Incorporated.
June 2, 1982. Comments on draft background information document.
6-49
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7.0 ENVIRONMENTAL IMPACT
7.1 INTRODUCTION
Volatile organic compound (VOC) emissions occur at a multitude of
sources within a synthetic fiber plant. These emissions occur both
inside and outside the plant during several processes, some of which
are polymer/solvent mixing and preparation, spinning, and fiber processing.
Chapter 6 discusses several model plants that were used to determine
VOC emissions from these various stages.
Total VOC emissions nationwide resulting from the manufacture of
the synthetic fiber types being investigated in this study were estimated
for 1982. This assumed fiber production at 95 percent capacity for
each plant. Estimates were made of emissions in 1987, assuming the
implementation of the various regulatory alternatives. Chapters 3
and 6 contain a more complete discussion of the Regulatory Alternative I
(baseline) emission levels.
This chapter presents an assessment of the regulatory alternatives
discussed in Chapter 6. The impacts of these alternatives associated
with air, solid waste, energy consumption, and other environmental
concerns will be discussed in the following sections.
7.2 AIR QUALITY IMPACT
The air pollution impact of each regulatory alternative is determined
by comparison of VOC emissions from various systems installed on the
appropriate process stages or points to control VOC emissions. In
order to analyze the incremental air quality impact of the resulting
levels of VOC emission reduction, annual VOC emission rates under each
regulatory alternative were determined and then employed to project
5-year impacts on national air quality.
Table 7-1 shows, for each fiber type, the amount of fiber produced
at synthetic fiber plants that would fall into one or more of the five
model plant categories. Production figures for 1987 for each fiber
7-1
-------
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type were derived by projecting the highest and lowest expected growth
rates as determined in the economic analysis (Chapter 9). The table
also projects the 1987 emissions and emission reductions resulting
from the implementation of each regulatory alternative. For the
purposes of this analysis, it is assumed that minor production increases
achieved through debottlenecking will not result in emission increases,
and would therefore not subject the facility to a new source standard.
7.2.1 Wet and Dry-Spun Acrylic and Modacrylic Fibers
Existing acrylic fiber production facilities were assumed to be
operating at essentially full capacity in 1982, The projected capacity
shortfall in 1987 is expected to be 73.6 Gg, in a high-growth scenario,
and zero Gg in a low-growth scenario. In order to meet the expected
demand under the high-growth scenario, two new facilities will be
required. Each facility will have an annual capacity of 45.4 Gg
(100 million pounds) (see Chapter 6). However, it is expected that
the facilities will only be operating at 81 percent capacity.
Assuming new plants are needed, the production increase in 1987 will
amount to a 20 percent cumulative increase over 1982 production. (See
Chapter 9 for further discussion of projected growth.)
There will be a corresponding increase in VOC emissions resulting
from this production increase. Under Regulatory Alternative I (baseline)
conditions, the expected emissions increase from facilities potentially
subject to the NSPS would be zero to 3,300 Mg/year, under the low- and
high-growth scenarios, respectively.
If Regulatory Alternative II were implemented, at these same
facilities, the annual emissions would be zero to 2,280 Mg, depending
on the growth rate. The emission reduction resulting from the
implementation of this alternative would be zero to 1,020 Mg/year.
If Regulatory Alternative III were implemented at these facilities,
the annual emissions would be zero to 1,320 Mg, depending on the
growth rate. The emission reduction resulting from the implementation
of this alternative would be zero to 1,980 Mg/year.
Since demand for acrylic fibers can be met substantially with
production from either wet or dry spinning processes, the two have
been combined for the purpose of estimating the environmental impact
7-3
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of increased production. As well, the impact of any new modacrylic
fiber production is considered; along with acrylic production.
7.2.2 Cellulose Acetate Cigarette Filtration Tow
Existing cellulose acetate filtration tow manufacturing facilities
were assumed to be operating at essentially full capacity in 1982.
The projected capacity shortfall in 1987 is expected to be 43.7 Gg
under a low-growth scenario and 95.1 Gg under a high-growth scenario.
In order to meet the expected (demand, two new facilities will be
required under the low-growth scenario, and four new facilities under
the high-growth scenario. (Each facility, as described in Chapter 6,
has an annual capacity of 22.7iGg (50 million pounds).) These facilities
are expected to operate at 95 percent capacity. The increase in
production from 1982 to 1987 is projected to be 43.1 Gg/year under the
low-growth scenario, and 86.3 Gg/year under the high-growth scenario.
This amounts to a 22 to 43 percent increase over the period. (See
Chapter 9.)
There will be a corresponding increase in VOC emissions resulting
from this production increase. Under Regulatory Alternative I (baseline)
conditions, the expected emissions increase from facilities potentially
subject to the NSPS would be 5J,170 to 10,350 Mg/year, under the low-
and high-growth scenarios, respectively.
If Regulatory Alternative II were implemented at these same
facilities, the annual emissions would be 2,890 to 5,780 Mg, depending
on the growth rate. The annual emission reduction resulting from
implementation of this alternative would be 2,280 to 4,570 Mg.
If Regulatory Alternative[III were implemented at these facilities,
the annual emissions would be 1,890 to 3,790 Mg, for the low- and
high-growth scenarios, respectively. The emission reduction resulting
from the implementation of thU alternative would be 3,280 to 6,560 Gg/year.
7.2.3 Cellulose Acetate Textile Yarn
It is assumed that all increases in demand for cellulose acetate
textile yarn between 1982 and 1987 will be met either through debottle-
necking or through increases in capacity utilization of equipment
already in place in 1982. (See Chapter 9 for an explanation of the
projections for this fiber type.) It is further assumed for the
purpose of this analysis that these modest increases in production
7-4
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will not result in emission increases, and would therefore not be
subject to an NSPS. (See Chapter 5 for further discussion of the
facilities potentially affected as a result of such modifications.)
Therefore, for the purpose of this analysis and projection of
environmental impact, there will be no emission reduction at acetate
textile yarn manufacturing plants between 1982 and 1987 resulting from
implementation of Regulatory Alternatives II or III.
7.2.4 Dry-Spun Spandex Fibers
By 1987, it is expected that an additional 0.5 to 2.5 Gg of
spandex will be produced annually. Additional capacity at up to one
new typical-size facility (potentially subject to an NSPS) will be
required to meet the expected demand. Baseline emissions from facilities
of this type are already lower than the levels that would be required
under either Regulatory Alternative II or III. Therefore, no model
plant or control options were developed to analyze the production of
this type fiber and the cost and effects of additional control equipment.
Assuming the emission levels at existing facilities are duplicated at
the new facilities, the expected emission increase in 1987 can be
estimated. Under the low-growth scenario, there would be essentially
no emission increase. Under the high-growth scenario, the emissions
increase would be 30 Mg annually. There would be no emission reduction
directly attributable to the implementation of the NSPS, since there
would be no regulatory impact except to ensure that any new facilities
perform at least as well as existing facilities.
7.2.5 Other Solvent-Spun Fibers
For the reasons given in Section 6.1, model plants and regulatory
alternatives were not devised for analysis of hypothetical new plants
producing all possible fiber types. However, it is possible that
there will be an increase in production of several fiber types for
which no model plants were developed. There would also be a corresponding
emission increase resulting from this new production. However, the
total of all these emission increases is expected to be substantially
lower than the increases from new production of the commodity fibers.
Therefore, for the purpose of evaluating the environmental impact of
the regulatory alternatives, no emission reduction attributable to the
7-5
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alternatives is considered for other solvent-spun fibers than those
specifically mentioned.
7.2.6 Total VOC Emission Reduction
Most VOC emissions from synthetic fiber manufacturing facilities
are generated at solvent-spun fiber production facilities, as explained
in earlier sections. Baseline emissions in 1980 from these facilities
are given in Table 3-9, in Chapter 3. These are the types of facilities
that would potentially be subject to an NSPS. Applying the appropriate
growth rates for affected fiber types and spinning methods, Regulatory
Alternative I emissions would increase by 5,170 to 13,680 megagrams
during the 1982-1987 period, depending on the collective industry
growth rate.
Under Regulatory Alternative II, a decrease in VOC emissions of
2,280 to 5,590 megagrams would b;e realized over the corresponding
baseline emissions under Regulatory Alternative I in 1987. This would
amount to a reduction of 41 to 4;4 percent. VOC emissions from the
manufacture of affected solvent-jspun synthetic fibers in 1987 under
Regulatory Alternative II controls would be 2,890 to 8,060 megagrams.
Regulatory Alternative III controls placed on the manufacture of
affected synthetic fibers would reduce VOC emissions from affected
facilities within the synthetic fibers industry 3,280 to 8,540 megagrams.
This would be a reduction of 62 to 63 percent from baseline emissions.
I • •
VOC emissions released from affected synthetic fiber manufacturing
plants in 1987 under Regulatory Alternative III controls would be
1,890 to 5,110 megagrams.
Emission reductions could be significantly greater than the
amounts indicated in this chapter. If new fiber manufacturing equipment
were installed at existing facilities, and the additions resulted in
overall emission increases, then the entire affected facility would
potentially be subject to the NS;PS. (See Chapter 5, Modification and
Reconstruction for further- discussion of applicability.) If the existing
facility were formerly generating VOC emissions at levels greater than
allowed under the NSPS, but were' to retrofit sufficiently to achieve
NSPS-allowed levels, then an emission reduction would be achieved that
is not specifically forecast in this chapter.
7-6
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7-2.7 Secondary Air Pollution Impact
Secondary air pollutants are those emissions which are not usually
associated with a baseline controlled facility, but which result from
the use of pollution control equipment required under Regulatory
Alternatives II or III. VOC emission control devices and techniques
which may be incorporated include, at a minimum, those discussed in
Chapter 4.
Secondary air pollution problems due to the use of carbon adsorption
are expected to be minimal. Gases may be emitted if the VOC stream
contacts the carbon bed before it is adequately cooled following
desorption. Proper cooling procedures following regeneration should
reduce thermal decomposition of VOC's.
Secondary air pollutants from scrubbers are not expected to be
significant, especially when compared to the contribution of pollutants
from other operations in a plant. The exhaust stream is typically
1 to 2 percent of the inlet vapor concentration. While incinceration
would result in reductions in the emissions of solvent vapor, there
would be significant secondary air pollution impacts, resulting from
the formation of oxides of nitrogen, oxides of sulfur, and carbon
monoxide. However, since recovery of solvents is essential to economical
operation, incineration is not expected to be a viable technique for
this industry.
7.3 WATER QUALITY IMPACT1"7
7.3.1 Model Plants Utilizing Scrubbers as Control Devices
Adverse environmental effects resulting from the operation of a
scrubber (absorber) could include improper disposal of the organic-laden
liquid effluent, undesired emissions from the scrubber stack resulting
from interaction within the scrubber, loss of absorbent to the atmosphere,
and increased water usage. However, add-on water scrubbing systems
usually mean only minimal increases in the existing water treatment
facilities at a plant.
Water used in scrubbing the solvent vapor from the gas stream is
piped to distillation columns where 98 to S9+ percent of the solvent
is separated from the water. The exact amount would depend on temperature,
solvent/water ratio, and the azeotrope formed by the solvent and
7-7
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water. The water stream leaving the column is normally routed back to
the process; thus any solvent remaining in the water would be reintroduced
to the process.
Water streams may also be directed to pi ant-operated waste treatment
I
facilities for disposal. The cpncentration of solvent in the waste
stream from the scrubber is very low, since maximum recovery of solvents
is necessary. Therefore, the actual solvent loading in the waste
stream sent to a waste treatment plant is expected to be minimal.
7.3.2 Plants Utilizing Aqueous!Salt Spinning Process in Acrylic Fiber
Manufacturing
Of the,various processes used in acrylic fiber production,, the
aqueous salt spinning processesigenerate the least VOC emissions.
This is the case since no organic solvent is introduced into the
process, and no VOC is volatilized during any of the spinning or
processing stages.
However, the use of a salt (zinc chloride or sodium thiocyanate,
for example) in aqueous solution creates potential water pollution
problems which must be alleviated in a wastewater treatment plant at
the manufacturing facility prior' to ultimate disposal. Since this
study addresses major VOC emission points and this type process has no
major solvent VOC emission points, then the aqueous salt spinning process
is excluded from consideration. There will, therefore, be no increased
water pollution impact at plants utilizing this process as a result of
the implementation of the NSPS.
7.4 SOLID WASTE IMPACT1'4~8
7.4.1 Plants Utilizing Distillation Columns as an Integral Part
of the Solvent Recovery System
A very minimal amount of organic material will accumulate and
form "still' bottoms," usually a heavy, tar-like compound, after extended
column operation. This material is typically removed during column
cleanout and landfilled. The amount of increase would be relative to
the increase in solvent recovered. Relative to the total amount of
solvent distilled and to the amount of "still bottoms" generated, the
increase due to the application of Regulatory Alternative II or III
would be negligible and not measurable.
7-8
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7.4.2 Filtration Media Disposal
Since the use of filter media is proportional to the amount of
polymer/solvent mixture filtered (and sent to spinning), any increase
in solvent recovery as a result of this NSPS would have no effect on
filtration media use. An increase or decrease in production rate,
however, would directly affect the quantity of filter media used and
disposed.
7.4.3 Plants Utilizing Carbon Adsorption9
Carbon adsorption is proposed as one of the alternative control
techniques in several of the model plants noted in Chapter 6. The
carbon in use is typically washed annually, and from 5 to 15 percent
(10 percent on the average) of the carbon is lost as fines at each
washing.
Although the increased requirement of carbon for collection of
incremental increases of solvent (due to the control alternatives)
should theoretically be proportional to the increased solvent con-
trolled, this study assumes no excess capacity exists at any given
carbon adsorption control device. Therefore, the smallest increase in
capacity of carbon adsorption is that of one totally new unit, consisting
of three adsorption beds (one in use, one cooling, and one desorbing).
Using existing units as models, the average bed contains approximately
25,000 pounds (11,300 kilograms) of carbon at 30 pounds/square foot
(480 kg/m ). A 3-bed unit will contain approximately 75,000 pounds
(34,000 kg) carbon, 10 percent of which will be lost (waste) annually.
Thus, the additional carbon waste generated as a result of Regulatory
Alternative II or III will be approximately 3,400 kg (7,500 pounds)
annually for each affected facility, or as much as 27,000 kg
(60,000 pounds) total for all such facilities.
7.4.4 Miscellaneous Waste Streams
Waste polymer and inorganic compounds from the polymer preparation
area are carried by the wastewater stream to the liquid waste system.
Waste polymer and inorganic compounds collected in the solvent recovery
system are usually processed to reduce solvent content. The resulting
solids are then mixed with water and pumped to the liquid waste system.
7-9
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Spun waste from the spinning area is washed to remove solvent and
is buried in a sanitary landfill, or redissolved in the appropriate
solvent and reintroduced into the process at the polymer/solvent
mixing area.
The main waste streams are from the polymer preparation area, the
solvent recovery area, and the domestic sewage. These streams are
reduced to sludge by standard wastewater treatment. Approximately
2,400 pounds per day are generated at a plant producing 100 million
pounds of fiber product per year. No measurable increase in the
amount of any sludge is expected from application of the proposed
control alternatives. ^
7.5 ENERGY IMPACT5'6>8>10
The fiber manufacturing industry is energy intensive, with substantial
amounts of electricity, coal, oil, and natural gas being consumed.
For example, a typical fiber plant producing 100 million pounds of
fiber annually will consume from 15 to 30 million kWh of electricity,
120 to 150 million tons of coal, 7,500 to 8,000 million cubic feet of
natural gas, and 400 to 600 thousand gallons of oil. (These figures
are for entire plants, however, and not only the affected facilities.)
With reference to solvent recovery, energy is required to supply
steam for carbon bed regeneration. The amount of steam required is
approximately 3 pounds of steam per pound of organic vapor adsorbed.
Energy in the form of a cooling water system is used to cool the gas
streams to optimum adsorption temperatures. Electrical energy is
required to move the large volumes of air utilized in the process.
Also, blowers are required to overcome the pressure drop encountered
by the gas moving through the adsorption bed. A balance must be
reached between the adsorption efficiency prescribed by the density
and thickness of the bed and the increased electrical requirement to
overcome the increased pressure drop.
The two regulatory alternatives above baseline control have
assumed grass roots installation of control devices will be required.
No existing excess capacity of control devices will be utilized in the
control analysis. Thus, the additional solvent recovered in the
various options is calculated to require new control devices, and the
7-10
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minimum additional energy requirement is that for operation of a new
scrubber or adsorption unit and the associated distillation columns.
.Typical energy requirements of an adsorption system are indicated
in Figure 7-1; an adsorber with an inlet flow rate of 20,000 scfm and
25 percent LEL will require 2.75 million BTU/hour (total energy requirement),
A scrubber operating at similar flow rates will require approximately
300,000 BTU/hour total energy input (see Figure 7-2).
For typical plants in the synthetic fibers industry, an increase
in energy consumption would result from compliance with either Alter-
native II or III. The increase will also depend on the growth rate of
a given fiber type. The incremental energy increase required to
operate the additional control equipment for each plant type under
Regulatory Alternatives II and III are shown in Table 7-2. Energy
requirements required under Regulatory Alternatives II and III in 1987
under a low-growth scenario would be 42 and 88 terajoules (39 and
83 billion Btu) per year, respectively. Energy requirements for
increased control at all affected facilities in 1987 under Alternatives II
and III would be 224 and 430 terajoules (210 and 403 billion Btu) per
year, respectively, in 1987 under the high-growth scenario. These
overall energy increases would amount to less than 3 percent of the
total energy (2,700 terajoules or 2,500 billion Btu) required to
operate all equipment at a typical synthetic fiber manufacturing plant
(not just the incremental control equipment).
7.6 OTHER ENVIRONMENTAL IMPACTS
No other adverse environmental impacts are expected to arise from
the implementation of standards of performance for synthetic fiber
manufacturing, regardless of the regulatory alternative selected as
the basis for standards.
7.7 OTHER ENVIRONMENTAL CONCERNS
7.7.1 Irreversible and Irretrievable Commitment of Resources
The alternative control systems will require installation of
additional equipment in new sources for each alternative emission
control system. This requirement will necessitate the additional use
of steel and other resources. The commitment of resources will be
small compared to national use of each resource. Ultimately, a large
quantity of these resources may be salvaged and recycled. No significant
7-11
-------
9oi -aaarioaa
Csl
OJ
7-12
-------
Table 7-2. ENERGY IMPACT3 OF REGULATORY ALTERNATIVES IN 1987
LOW-GROWTH SCENARIO
Fiber Type Regulatory Alternative IIb
Acrylic/
Modacrylic 0 terajoules
Acetate Filter
Tow 42 (21)3
Acetate
Filament Yarn 0
Regulatory Alternative III
0 terajoules
88 (44)3
0
Total
42 terajoules
88 terajoules
HIGH-GROWTH SCENARIO
Fiber Type
Acrylic/
Modacrylic
Regulatory Alternative IIb Regulatory Alternative IIIb
140 (70)c terajoules 254 (127)c terajoules
Acetate Filter
Tow
Acetate
Filament Yarn
84 (21)c
0
176 (44)
0
Total
a
224 terajoules
430 terajoules
These values reflect the energy impact of the expected number of
affected facilities in operation in 1987.
3These energy impacts are the incremental energy required to operate
additional control equipment required by the alternatives.
'The numbers in parentheses represent the impact of a single affected
facility.
7-13
-------
amounts of space (or land) are required to install control equipment
because all control systems can be located within little additional
space. Therefore, negligible land commitment is expected for additional
control devices.
7.7.2 Environmental Impact of I Delayed Standards
Delay of standards proposal for the synthetic fiber manufacturing
industry will haye minor negative environmental effects on water and
solid waste. However, delay in implementation of standards will
generate additional VOC emissions at the significant rates described
earlier in this chapter.
No emerging emission control technology appears imminent that
could achieve greater emission[reductions or result in lower costs
than those represented by the emission control alternatives considered
here. Consequently, delaying standards to allow further technical
developments appears to present; no tradeoff of higher solvent emis-
sions in the near future for lower emissions in the longer term.
7.7.3 Environmental Impact of ;No Standards
Growth projections are presented in Chapter 9. The increase in
production of organic solvent spun fibers will cause or contribute
significantly to nationwide VOC emissions, should no additional control
be imposed. The administrator ,has found that this may reasonably be
anticipated to endanger public health or welfare.
Essentially no adverse water and solid waste impacts are associated
with the alternative emission control systems proposed in this section.
Therefore, as in the case of delayed standards, there is no tradeoff
of potentially adverse impacts in these areas against the negative
result on air quality that would result from nonimplementation of
i
additional control.
7-14
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7.8 REFERENCES
1. Report of the Initial Plant Visit to American Cyanamid Company
Santa Rosa Plant, Milton, Florida. Prepared for the Office of
Air Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. April 11, 1980.
2. Report of the Plant Visit to Badishe Corporation Synthetic Fibers
Plant, Williarnsburg, Virginia. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. November 28, 1979.
3. Report of the Initial Plant Visit to DuPont Corporation Waynesboro
Plant, Waynesboro, Virginia. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific .Environmental Services,
Inc. Research Triangle Park, North Carolina. May 1, 1980.
4. Report of the Initial Plant Visit to DuPont Corporation May
Plant, Camden, South Carolina. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North'Carolina. April 29, 1980.
5. Report of the Initial Plant Visit to Monsanto Company acrylic
fiber plant, Decatur, Alabama. Prepared for the Office of Air
Quality Planning and Standards, U.S. Environmental Protection
Agency, during development of New Source Performance Standards
for the synthetic fibers industry. Pacific Environmental Services,
Inc. Research Triangle Park, North Carolina. April 1, 1980.
6. Report of Initial Plant Visit to Tennessee Eastman Company,
Kingsport, Tennessee. Prepared for the Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency,
during development of New Source Performance Standards for the
synthetic fibers industry. Pacific Environmental Services, Inc.
Research Triangle Park, North Carolina. December 13, 1979.
7. Report of the Plant Visit to Globe Manufacturing Company, Gastonia,
S.C. U.S. Environmental Protection Agency. Office of Air Quality
Planning and Standards. Research Triangle Park, N.C. December 1,
1981.
7-15
-------
8. Reports of the Phase II Pl;ant Visit to Celanese Fibers Company
Celriver acetate plant, Najrrows, Virginia. Prepared for the
Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, during 'development of New Source Performance
Standards for the synthetic fibers industry. Pacific Environmental
Services, Inc. Research Triangle Park, North Carolina, flay 28,
1980.
9. Cheremisinoff, P.M. and Eljlerbusch, Fred. Carbon Adsorption
Handbook. Ann Arbor Science Publishers, Incorporated. 1978.
10. Report of Phase II Plant Visit to Celanese Fibers Company Celco
acetate plant. Rock Hill,; South Carolina. Prepared for the
Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, during development of .New Source Performance
Standards for the synthetic fibers industry. Pacific Environmental
Services, Inc. Research Triangle Park, North Carolina. August
11, 1980.
7-16
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8.0 COST ANALYSIS
8,1 SYNTHETIC FIBERS COST ANALYSIS OF REGULATORY ALTERNATIVES
8.1.1 Introduction
The following sections present estimates of the capital and • -- •
annual costs for each model plant and regulatory alternative described
in Chapter 6.0. These cost estimates are used to ascertain the economic
impact of the regulatory alternatives upon the solvent spun synthetic
fibers industry in Chapter 9.0. To ensure a common cost basis, Chemical
Engineering cost indices were used to adjust both process and control
equipment to mid-1980 dollars.
This chapter also includes estimates of the cost effectiveness of
each alternative. Cost effectiveness is typically estimated by comparing
the total annualized control cost to the annual reduction of emissions
achieved. The various control alternatives are ranked based on their
relative cost effectiveness in Section 8.4.
8.1.2 Model Plants/Regulatory Alternatives
As explained in Chapter 6, the five model plants were developed
to be representative of the portion of the synthetic fibers industry
which includes wet and dry solvent spinning of the fiber. The models
describe two fiber types, acrylic and cellulose acetate. All fiber
types considered are solvent spun; wet spun acrylic fibers employ
dimethylacetamide; dry spun acrylics use dimethylformamide; dry spun
modacrylic,. eellulose acetate filament, and cigarette tow all employ
acetone as a spinning solvent.
8.2 .NEW FACILITY COSTS
8.2.1 Baseline Model Plant Costs
The baseline model plants were developed to be representative of
basic organic solvent-spun manufacturing processes that in EPA's
judgment are most likely to be constructed in the absence of additional
8-1
-------
regulatory action. Baseline capital costs include the costs for tank
farms, chemical receiving and storage, dope preparation equipment,
spinning equipment, fiber processing equipment, solvent recovery
equipment, manufacturing buildings, warehouse, quality control
laboratory, and other ancillary manufacturing facilities and equipment.
Not included in baseline capital costs are utility generation, waste
treatment, streets, parking, land [purchase,, and general support facilities
(cafeteria, medical facilities, administrative offices). The baseline
annual costs are the costs of operating and maintaining the facility.
These include direct costs such as operating labor, maintenance labor
and equipment, utilities, and laboratory charges; fixed charges of
local taxes and insurance; and other general expenses such as plant
overhead, administration, and research. These costs do not include a
depreciation factor.
The purpose for estimating the baseline costs of the five model
plants in question is to demonstrate the difference in annualized
capital and operating costs among the various spinning techniques.
Table 8-1 presents these costs along with the capital costs associated
with the baseline solvent recovery systems, which capture solvent only
from the spin cells, cabinets, or baths.
•
8.2.2 Costs of Regulatory Alternatives
This section summarizes the assumptions used in developing the
control costs for the model plants and various control options. The
technical operating parameters are presented in Chapter 6 and are not
repeated here. Table 8-2 presents capital and annual operating costs
associated with Regulatory Alternatives II and III. Table 8-3 compares
capital and annual operating costs under Alternatives II and III that
additional emission control systems would add to the baseline costs.
Under Alternative II the additional costs of recovery equipment would
add 2.9 to 9.8 percent to the baseline capital costs and an additional
1.1 to 4.5 percent to baseline anrjual operating costs, depending on
the model plant in question. Under Alternative III capital costs
would increase by 6.3 percent to 12.4 percent; annual operating costs
would increase by 1.9 to 6.3 percent, depending on the model plant in
question.
8-2
-------
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-------
TABLE 8-2. CAPITAL AND ANNUAL OPERATING COSTS
ASSOCIATED WITH MODEL PLANT OPTIONS
(Millions of dollars)
Model Plant
Regulatory Alternative I
(Baseline)
Capital Costs
Annual
Operating Costs
Regulatory Alternative II
Capital Costs
Annual
Operating Costs
Regulatory Alternative III
Capital Costs
Annual
Operating Costs
72.2
51.6
69.5
46.3
45.1
23.1
67.1
25.7
83.. 6
27.1
76.0 72.5 46.4 70.1 91.8
52.2 46.8 23.4 26.4 28.5
78.7 75.0 48.1 71.3; 94.0
52.6 47.2 23.7 26.6: 28.8
NOTES: 1. Figures above for annual costs do not include recovery credits
for solvent, or capital 'recovery costs.
2. Costs are presented for entire affected facility, with
incremental additional costs included in figures for
Regulatory Alternatives II and III.
3. Annual costs do not include raw materials processed, i,,e.,
polymer, finish, and solvent.
8-4
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Tables 8-4 through 8-8 display the capital outlay expenditures
and annualized costs for each regulatory alternative for model plants
1 through 5. All equipment associated with absorption/adsorption
stripping columns are expressed as a fractional function of the major
equipment costs in Table 8-9. From these initial investments, one can
estimate such capital related changes as plant overhead, property
taxes, insurance, and general administration; these charges are called
fixed annual operating costs. To them are added recurring direct
costs such as utilities, materials, and labor for operation and maintenance
of the equipment during its life.! These annual costs do not include
the costs of .capital and depreciation, raw materials, and distribution
or selling costs. Table 8-10 provides the basis for estimating the
annual operating costs for the regulatory alternatives for model
plants 1 through 5; these estimates are presented in Tables 8-4 through 8-8.
Credits for increased amounts of recovered solvent resulting from
increased capture and control of solvent vapor are not presented.
8.3 MODIFIED OR RECONSTRUCTED FACILITIES
As defined in Chapter 5 of this report, synthetic fiber facilities
may undergo "modification" or "reconstruction" thereby bringing the
facility under the purview of the standard. Retrofitting solvent
recovery equipment to existing synthetic fiber plants poses certain
problems. The amount of physical space necessary to install ventilation
ductwork to capture and transport solvent from process lines is a
definite constraining factor. Equipment and personnel must be able to
move along process line aisles without being excessively hindered;
therefore, installation of enclosures at some existing facilities is
not possible without a complete reconstruction of the entire spinning
area.
Scrubbers, condensers, distillation columns, and carbon beds
require additional utility distribution systems and larger load capacities
to accommodate them. This could cause an overload problem at existing
plants. Additional utility equipment may also pose space problems.
The cost of installing a control system in an existing plant that
has been modified, reconstructedI or expanded may be greater than the
cost of a system for a new faciljity with the same exhaust gas parameters
because of special design considerations. In retrofitting systems,
8-6
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Table 8-4. COMPONENT CAPITAL COSTS AND OPERATING COSTS FOR
MODEL PLANT 1, ALTERNATIVE II AND III
Direct Costs
1) Equipment Costs
Enclosures
Ducting ,
Adsorption/Stripping Columns
Fan, Pumps, Compressors
Instruments and Controls
Taxes
Freight
Total
2) Installation Direct Costs
Foundations and Supports
Erection and Handling
Electrical
Piping
Insulation
Painting
Site Preparation
Facilities and Buildings
Total
3) Installation Indirect Costs
Engineering and Supervision
Construction and Field Expenses
Construction Fees
Start-up
Performance Test
Contingencies
Total
Grand Total
DIRECT OPERATING COSTS
1) Operating Labor
a) Operator
b) Supervisor
2) Operating Materials
3) Maintenance
a) Labor
b) Material
4) Utilities
5) Waste Disposal
INDIRECT OPERATING COSTS
6) Overhead •
7) Property Tax
8) Insurance
9) Administration
Total Cost
CREDITS
10) Recovered Solvent
Component
Alternative II
Pol 1 ars
605,000
183,000
284,000
36,000
16,600
33,200
83,100
1,240,900
133,000
664,800
11,100
332,040
11,100
11,100
55,400
554,000
1,772,900
166,200
166,200
221,600
11,100
11,100
221,600
797,800
$3,811,600
Operat
Alternative II
Dollars
54,000
8,100
7,500
54,000
25,000
152,500
38, 100
117,800
38,100
38, 100
76,200
$609,400
570,000 kg/yr
Capital Costs
Alternative III
Do! 1 ars
806,500
274,500
723,000
79,000
28,200
56,500
141,200
2,108,900
226,000
1,129,800
18, 800
564,900
18,800
18,800
94,200
941,500
3,012,800
282,500
282,500
376,600
18,800
18,800
376,600
1,355,800
$6,477,500
ing Costs*
Alternative III
'Dollars
54,000
8,100
12,000
54,000
50,000
306,800
64,800
142,900
64,800
64,800
129,600
$951,800
1,140,000 kg/yr
*Annualized capital costs not included; see Table 9-34.
8-7
-------
Table 8-5. COMPONENT CAPITAL COSTS AND OPERATING COSTS FOR
MODEL PLANT 2, ALTERNATIVE II AND III
Direct Costs
Component Capital Costs
Alternative II Alternative III
Dollars
Do!1ars
1) Equipment Costs
Enclosures
Ducting
Adsorption/Stripping Columns
Fan, Pumps, Compressors
Instruments and Controls
Taxes
Freight
Total
2) Installation Direct Costs
Foundations and Supports
Erection and Handling
Electrical
Piping
Insul ation
Painting
Site Preparation
Facilities and Buildings
Total
3} Installation Indirect Costs
Engineering and Supervision
Construction and Field Expenses
Construction Fees
Start-up
Performance Test
Contingencies
Total
Grand Total
DIRECT OPERATING COSTS
1) Operating Labor
a) Operator
b) Supervisor
2) Operating Materials
3) Maintenance
a) Labor
b) Material
4} Utilities
5) Waste Disposal
INDIRECT OPERATING COSTS '
6) Overhead
7 I Property Tax
8) Insurance
9) Administration
Total Costs
CREDITS ...
10) Recovered Solvent •• :.'
484,000
137,500
212,500
32,000
13,000
26,000
65,000
970,000
104,000
519,600
8,700
259,800
8,700
8,700
43,300
433,000
1,385,600
129,900
129 ,900
173,200
8,700
8,700
173,200
623,500
$2,979,200
Operating
Alternative II
Pol 1 ars
54,000
8,100
5,900
54,000
20,000
119,200
29;, 800
' 113, 000
29,800 "
29,800
59,600
$523,200
570,000 kg/yr
'605,000
255,500
656,500
79,000
23,900
47,900
119,700
1,787,500
191,500
957,600
16,000
478,800
15,900
16,000
79,800
798,000
2,553,600
239,400
239,400
319,200
16,000
16,000
319,200
'1,149,200
$5,490,300 ,
Costs*
Alternative III
Dol 1 ars
54,000 :
8,100
• 10,000
54,000 , ' -•
40,000
319,200
48, -000
133,000
55; 000 ' .
- 55,000
110,000
$886,300
1,173,000 kg/yr
*Annua1ized capital costs-not included;'see Table 9-34..
8-8
-------
Table 8-6. COMPONENT CAPITAL COSTS AND OPERATING COSTS FOR
MODEL PLANT 3, ALTERNATIVE II AWD III
Component Capital Costs
Alternative II Alternative III
Direct Costs
1) Equipment Costs
End osu res
Ducting
Adsorption/Stripping Columns
Fan, Pumps, Compressors
Instruments and Controls
Taxes
Freight
Total
2) Installation Direct Costs
Foundations and Supports
Erection and Handling
Electrical
Piping
Insulation
Painting
Site Preparation
Facilities and Buildings
Total
3) Installation Indirect Costs
Engineering and Supervision
Construction and Field Expenses
Construction Fees
Start-up
Performance Test
Contingencies
Total
Grand Total
Dollars
125,000
230,000
22,000
5,700
11,300
28,300
45,200
226,200
3,800
113,100
3,800
3,800
18,900
188.500
603,300
56,500
56,500
75,400
3,800
3,800
• 75.400
$1,297,000
Dollars
248,000
235,000
353,000
36,000
13,100
26,200
65,400
976,700
104,600
523,200
8,700
261,600
8,700
8,700
43,600
436.000
1,395,100
130,800
130,800
174,400
8,700
8,700
174,400
$2,999,600
DIRECT OPERATING COSTS
Operating
Alternative II
Dollars
Costs*
Alternative III
1) Operating Labor
a) Operator
b) Supervisor
2) Operating Materials
3) Maintenance
a) Labor
b) Material
4) Utilities
5) Waste Disposal
INDIRECT OPERATING COSTS
6) Overhead
7) Property Tax
8) Insurance
9) Administration
Total Costs
CREDITS
10) Recovered Solvent
54,000
8,100
4,300
54,000
13,000
45,200
12,900
105,900
12,900
12,900
26,000
$349,200
1,024,000 kg/yr
54,000
8 100
10 \ 500
54,000
31,500
134,000
30,000
124,400
30,000
30,000
60,000
$566,500
1,980,000 kg/yr
*Annualized capital costs not included; see Table 9-34.
8-9
-------
Table 8-7. COMPONENT CAPITAL COSTS AND OPERATING COSTS FOR
MODEL PLANT 4, ALTERNATIVE II AND III
Direct Costs
1) Equipment Costs
End osu res
Ducting
Adsorption/Stripping Columns
Fan, Pumps, Compressors
Instruments and Controls
Taxes
Freight
Total
2) Installation Direct Costs
Foundations and Supports
Erection and Handling
Electrical
Piping
Insulation
Painting
Site Preparation
Facilities and Buildings
Total
3) Installation Indirect Costs
Engineering and Supervision
Construction and Field Expenses
Construction Fees
Start-up
Performance Test
Contingencies
Total
Grand Total
DIRECT OPERATING COSTS
1) Operating Labor
a) Operator
b) Supervisor
2) Operating Materials
3) Maintenance
a) Labor
b) Material
4) Utilities
5) Waste Disposal
INDIRECT OPERATING COSTS
6 Overhead
7 Property Tax
8 Insurance
9 Administration
Subtotal
SHUTDOWN COSTS
10) Labor and Lost Production
Total Costs
CREDITS
11) Recovered Solvent
Component Capital Costs
Alternative II Alternative III
Dollars Pol 1 ars
242,000 423,000
120,000 180,000
650,000 820,000 :
100,000 125,000
111,200 154,800
33,400 46,500
83,400 116,100
1,340,000
89,000
155,700
44,500
22,200
11,100
11,100
55,600
556,000
945,200
166,800
83,400
222,400
22,200
11,100
• 222,400
$3,013,500
Operating
Alternative II
Pol 1 ars
54,000
8,100
7,500
54,000
90,400
42,300
30,100
176,800
30,100
30,100
60,200
583,600
120,000
$703,600
1,140,000 kg/yr
1,865,400
123,800
216,700 '
61,900
30,900
15,500
15,500
77,400
774,000
1,315,700
232,200
116,100
309,600
30,900
15,500
309,600
1,013,900'
$4,195,000
Costs*
Alternative III
Don ars
54,000
8,100
19,000
54,000
125,800
105,000
41,900
166,600
41,900
41,900
83,800
742,000'
120.000
862,000 ;
1,620,000 kg/yr
*Annualized capital costs not included; see Table 9-37.
8-10
-------
Table 8-8. COMPONENT CAPITAL COSTS AND OPERATING COSTS FOR
MODEL PLANT 5, ALTERNATIVE II AND III
Direct Costs
1) Equipment Costs
Enclosures
Ducting
Adsorption/Stripping Columns
Fan, Pumps, Compressors
Instruments and Controls
Taxes
Freight
Total
2) Installation Direct Costs
Foundations and Supports
Erection and Handling
Electrical
Piping
Insulation
Painting
Site Preparation
Facilities and Buildings
Total
3) Installation Indirect Costs
Engineering and Supervision
Construction and Field Expenses
Construction Fees
Start-up
Performance Test
Contingencies
Total
Grand Total
DIRECT OPERATING COSTS
1) Operating Labor
a) Operator
b) Supervisor
2) Operating Materials
3) Maintenance
a) Labor
b) Material
4) Utilities
5) Waste Disposal
INDIRECT OPERATING COSTS
6) Overhead
7) Property Tax
8) Insurance
9) Administration
Total Costs
CREDITS
10) Recovered Solvent
Component Capital Costs
Alternative II Alternative III
Dol 1 ars Do! 1 ars
1,750,000
1,210,000
155,000
46,700
93,500
233,600
3,488,800
249,200
436,100
124,600
62,300
31,200
31,200
155,700
1,557,500
2,647,800
467,300
233,600
623,000
62,300
31,100
. 623,000
2,040,300
$8,176,900
Operating
Alternative II
Dol 1 ars
54,000
8,100
'102,700
54,000
245,300
205,300
81,800
331,700
81,800
81,800
163,500
$1,410,000
1,600,000 kg/yr
1,950,000
1,835,000
187,000
59,600
119,200
297,900
4,448,700
317,700
556,000
158,900
79,400
39,700
39,700
198,600
1,986,000
3,376,000
595,800
297,900
794,400
79,400
39,700
794,400
2,601,600
$10,426,300
Costs*
Alternative III
Pol 1 ars
54,000
8,100
119,600
54,000
285,000
239,100
104,300
371,400
104,300
104,300
208,600
$1,652,700
2,240,000 kg/yr
*Annualized capital costs not included; see Table 9-37.
8-n
-------
TABLE 8-9. COMPONENT CAPITAL COST FACTORS
FOR ABSORPTION/ADSORPTION STRIPPING
AS A FUNCTION OF EQUIPMENT COSTS
Direct Costs
Equipment, f.o.b.
Manufacturer
Instruments and Controls
Taxes
Freight
Foundations and Supports
Erection and Handling
Electrical
Piping
Insulation
Painting
Site Preparation
Facilities and Buildings
Absorption Factor Adsorption Factor
1.000
0.015
0.030
0.075
0.120
0.600
0.010
0.300
0.010
0.010
0.050
0.500
1.000
0.015
0.030
0.075
0.080
0.140
0.040
0.020
0.010-
0.010
0.050
0.500
Indirect Costs
Engineering and Supervision
Construction and Field Expenses
Construction Fee
Start-up
Performance Test
Contingencies
0.150
0.150
0.200
0.010
0.010
0.200
0.150
0.075
0.200
0.020
0.010
0.200
NOTES: 1. Ducting costs include all ductwork, elbows, tees, expansion
joints, dampers, and transition pieces of stainless steel.
2. Costs include stainless steel components on adsorbers.,
absorption column internals, distillation column internals,
condensers, and piping where solvent liquid or vapor
contacts surface.
3. Distillation columns are included as a cost of each control
option regardless of solvent recovery method. This scenario
was assumed in order to provide a worst-case cost. Critical
design parameters for Costing the distillation (stripping)
columns included column diameter, number of plates, type
and spacing of plates,'operating pressure, heat input to
the reboiler and heat output from the condenser.
8-12
-------
TABLE 8-9. COMPONENT CAPITAL COST FACTORS
FOR ABSORPTION/ADSORPTION STRIPPING
AS A FUNCTION OF EQUIPMENT COSTS (Concluded)
NOTES: 4. Carbon adsorber costs are for basic custom built systems,
not package units. Equipment costs include preconditioning,
blowers, three adsorbers, activated carbon, condenser,
storage tank, all process valves, distillation system,
instrumentation/controls, and accessories.
5. Absorption and stripping columns are bubble cap tray and
plate towers. The costs of absorption and stripping towers
are a function of the size, thickness, and materials of
construction. The design parameters used in costing
include the column diameter, column height, operating
pressure, column pressure drop, number of transfer units,
tray efficiency, tray spacing, tray material, column shell
material, thickness of shell wall, and liquid and gas flow
rates. The cost of the fabricated vessel includes the
cost of the shell plus the cost of two heads, a skirt for
support, flange-type nozzles. To these are added the tray
cost and support plates. Ancillary equipment such as fans
and blowers are included under separate entry.
6. In order to avoid the potential build-up of an explosive
concentration, air flow and solvent concentration monitoring
instrumentation with machine shutdown capability are
included in Model Plant 4 costs under "Instrument and
Controls." Multiple monitors and numerous monitoring
locations are incorporated for redundancy and added safety
margin. Also included in the costs for "Fans, Pumps,
Compressors" are the costs associated with back-up exhaust
fans with power for operation received from two independent
sources (e.g., electrical and steam turbine). Back-up may
also involve a nonelectrical means of purging such as
steam jet ejectors which could force the solvent/air
mixture out of the enclosures. The equipment costs asso-
ciated with the prevention of excessive risk amount to
about 10 percent of the total capital cost of the control
options.
7. Model Plant 5 costs for adsorption/stripping columns
include extensive pretreatment of the gas stream for
contaminant removal and dehumidification. The equipment
consists of filter, cooler, and reheater to condition the
gas before entering the adsorbers.
8-13
-------
TABLE 8-10. BASIS FOR ESTIMATING ANNUAL OPERATING COSTS
FOR REGULATORY ALTERNATIVES
Direct Operating Costs
Operating Labor
Direct Operator
Supervision
Operating Materials
Maintenance
Labor
Materi al
Utilities
Water
Electricity
Steam
Waste Disposal
Indirect Operating Costs
Overhead
Property Tax
Insurance
Administration
Credits
Recovered Solvent.
$108,000/yr/rnan/shift
15 percent of direct labor
Per plant control process
Equal to operating labor
3 percent of total capital costs
$0.25/1000 gal.
$0.04/kWh
$4.0/1000 Ibs.
L percent of total capital costs
80 percent of operating and maintenance
Tabor plus maintenance materials
1 percent of total capital costs
1 percent of total capital costs
2 percent of total capital costs
Dependent on specific plant process and
recovery system
NOTE:
Model Plant 4 annual operating cost includes the costs of shutdown of the
spinning machines- resulting from the. application and use of enclosures on the
spin cell exits and tow line-. The costs represent the increased labor necessary
to restart the machines and the. production lost during the shutdown period.
8-14
-------
additional costs may be encountered because of such items as demolition
requirements, crowded construction working conditions, scheduling
construction activities with production activities, and longer inter-
connecting piping. Availability of space, additional ducting, and
additional engineering must be considered. These constraints must be
taken into account when costing the retrofitting of recovery equipment
at synthetic fiber plants. Estimating the additional installation
cost or retrofit penalty is dependent on the many factors peculiar to
the individual plant.
Configuration of equipment in the existing plant governs the
location of th.e control system. Depending on process or stack location,
long ducting runs from ground level to the control device, stack, and
reprocessing equipment may be required. Costs may increase considerably
if the control equipment must be placed on the roof and requires steel
structural support. It is estimated that rooftop installation can
double the structural costs. In addition, labor would probably have
to be done at premium wage rates in accordance with governmental
regulations and/or union agreements. Other cost components that may
increase because of space restrictions and plant configurations are
contractor's fees and engineering fees, which are estimated at 15 percent
and 20 percent for a new facility, but may be expected to increase to
20 percent and 30 percent for a retrofit. These fees depend on the
difficulty of the job, the risks involved, and the current economic
conditions.
The annual operating costs of control systems for
modified/reconstructed facilities are calculated similarly to those
for new facilities. The cost items may be equal to or greater than
costs for new facilities, depending on the specific layout of the
control equipment and affected facility.
8.4 COST EFFECTIVENESS
8.4.1 Model Plants
Cost effectiveness, expressed in annualized costs per megagram of
emission reduction, for Regulatory Alternatives II and III for model
8-15
-------
plants 1 through 5 are presented in Tables 8-11, 8-12, and 8-13. All
costs, production levels, emission reductions, etc., are based on
model plant parameters described; in Chapters 6 and 8.
Under Alternative II, model plant 1 shows a zero cost effectiveness
when compared to baseline, Alternative I; the costs of controls for
emission reduction are offset by; the value of the recovered solvent.
Model plant 3 shows a net gain of $182/Mg under Alternative II; the
additional solvent that could be recovered beyond baseline would
result in decreased annualized costs. Model plants 2, 4, and 5 show
positive cost effectiveness of $166, $166, and $588 per Mg VOC reduction,
respectively, when compared to Alternative I.
Under Alternative III, model plants 1 and 3 show a net gain or
annual savings of $350 and $193 per Mg of emission reduction, respectively,
when compared to the baseline. Model plant 2 would experience a zero
cost effectiveness under this alternative. However, model plants 4
and 5 would incur positive increases in annual costs of $120 and $442
per Mg of emission reduction, respectively, above the baseline case.
Compared to Alternative II, the application of Alternative III to
the model plants would result in decreased annualized costs Of control
and thus in decreasing cost per Mg of emission reduction, as presented
in Table 8-13.
8.4.2 Projected 1987 Cost Effectiveness
The projected capacity shortfalls as presented in Tables 9-20 and
9-30 of Chapter 9 lead to the following conclusions concerning likely
capacity additions by synthetic fiber producers by 1987:
(1) The projected capacity shortfall arising from the high growth
projection for acrylic and modacrylic fibers would support additional
plant capacity. For this analysis, it is assumed that capacity is
constructed-in increments of model plant capacity, and that plants of
model plant 2 type would be built. Two plants, each with 45.36 Gg
capacity, would be constructed by 1987 since there would be significant
capacity shortfall if only one were constructed. These two plants
would each operate at 81 percent capacity utilization in 1987. (Table 9-11
in this BID indicates that this capacity utilization rate is well
within the range of historical values.)
8-16
-------
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8-19
-------
(2) The projected capacity shortfall arising from the low growth
projection for acrylic and modacrylic fibers would not support additional
capacity. This shortfall would likely be met by debottlenecking
current production processes.
(3) The projected capacity shortfall arising from the high growth
projection for cigarette filtration tow would support additional
capacity by 1987. Again, it is assumed that capacity is constructed
in increments of model plant capacity. Four plants, each with 22.7 Gg
capacity, would be constructed. These four plants would each operate
at 95 percent capacity utilization. A capacity shortfall of 4.3 Gg
would still exist, but this shortfall would not support an additional
plant.
(4) The projected capacity shortfall arising from the low growth
projection for cigarette filtration tow would also support additional
plant capacity by 1987 (capacity that would be constructed in increments
of model plant capacity). Two plants, each with 22.7 Gg capacity,
would be constructed. These two plants would each operate at 95 percent
capacity utilization. Excess capacity of 1.7 Gg would exist.
(5) The projected capacity shortfalls arising from either the
nigh or low growth projections for cellulose acetate textile yarn
would not support additional capacity by 1987.
Based on the above conclusions, comparisons of annualized costs
per megagram of emission reduction were made for those plants that are
most likely to be built in the next 5 years. All three regulatory
alternatives were examined. Compared to the baseline, Alternatives II
and III result in emission reductions of 5.6 and 8.5 Gg/year, respectively,
by 1987. Using these emission reduction figures, annual ized costs per
megagram of emission reduction for typical plants would be as much as
$392 and $2Q2, respectively, for Alternatives II and III.
At these same plants, Alternative III would result in an annual
total emission reduction of. about 3.0 Gg/year more than Alternative II.
Alternative III would have an annual cost of $2.4 million more than
Alternative II; however, the value of the additional solvent recovered
would decrease the annual cost by roughly the same amount. Thus,
there would be no net cost per megagram of emission reduction to the
industry in implementing Alternative III over Alternative II. Table 8-14
presents the projected 1987 cost effectiveness of the regulatory alternatives,
8-20
-------
Table 8-14. PROJECTED 1987 COST EFFECTIVENESS
OF REGULATORY ALTERNATIVES
Growth
Scenario
1982-1987
Number of
Affected
Facilities
1987
Alternative II*
Solvent
Credit
(105$)
Alternative III1
Solvent Credit
Baseline
Annual Cost
(106$/yr)
Alternative II
Annual Cost
(106$/yr)
Alternative III
Annual Cost
(106$/yr)
Alternative II
Net Annual Cost
(106$/yr)
Alternative III
Net Annual Cost
(106$/yr)
Alternative II
Emission
Reduction (Mg)
Alternative III
Emission
Reduction (Mg)
Alternative II
Cost
Effectiveness
($/Mg)
Alternative III
Cost
Effectiveness
($/Mg)
Acrylic/Modacrylic
high low
2 0
1.1 0.0
2.2 0.0
108.0 0.0
108.4 0.0
108.4 0.0
0.4 0.0
0.4 0.0
1020
1980
392
202
Cellulose Acetate 1
Filter Tow | Totals
high low
4 2
3.0 1.5
4.3 2.1
128.0 64.0
128.8 64.4
128; 8 64.4
0.8 0.4
0.8 0.4
4570 2280
6560 3280
175 175
122 122
high low
6 2
4.1 1.5
6.5 2.1
236.0 64.0
237.2 64.4
237.2 64.4
1.2 0.4
1.2 0.4
5590 2280
8540 3280
215 175
141 122
*Amount of solvent recovered multiplied by solvent cost, $1.09/kg DMF and
$0.62/kg acetone.
8-21
-------
8.5 REFERENCES
1. Neveril, R.B. et.al. Capital and Operating Costs of Selected Air
Pollution Control Systems. CARD, Inc. EPA-450/5-80-002.
December 1978. pp. 5-31 to 5-38 and 5-50 to 5-65.
2. Air Pollution Engineering Manual. AP-40. Environmental Protection
Agency. OAQPS. May 1973. pp. 220-227.
3. Foust, A.S., et. al. Principles of Unit Operations. John Wiley
& Sons, Incorporated., 1960. pp. 11-14.
4. McCabe, W.L. and Smith, J.C. Unit Operations of Chemical Engineering,
Second Edition. McGraw-Hill iBook Company. 1967. pp. 517-539.
5. Reference 4, pp. 549-607.
6. Peters, M.S. and Timmerhaus, K.D. Plant Design and Economics for
Chemical Engineers. McGraw-Hill Book Company, Second Edition.
1968. pp. 614-655.
7. Vatavuk, W.M. and Neveril, R.B. Estimating Costs of Air Pollution
Control Systems; Part I: Parameters for Sizing Systems. Chemical
Engineering. October 6, 1980. pp. 165-168.
8. Handbook of Chemistry and Physics, Forty-Eighth Edition. The
Chemical Rubber Company. 1967. pp. F-10.
9. Perry, R.H. et. al. Section 14: Gas Absorption and Solvent
Extraction. Chemical Engineer's Handbook. McGraw-Hill Book
Company, Fourth Edition. 1963. pp. 14-24 through 14-34.
10. Reference 9, Section 18: Liquid-Gas Systems, pp. 18- through 18-25.
11. Reference 9, Section 13: Distillation, pp. 13-7, 13-21 through
13-29, 13-51 through 53.
12. Calvert, J. et. al. "Wet Scrubber System Study" Volume I. Scrubber
Handbook. APT, Incorporated. EPA R2-72-118A, CPA 70-95.. duly
1972.
13. Letter from Zerbonia, R.A., PES, Incorporated, to Natho Massey,
AAA Technology and Special Company, Incorporated. September; 3,
1980. Use of "Concept Program to Simulate Absorption/Distillation
Columns.
14. Letter and attachments from Massey, N.A., Process Simulation
Consultant, AAA Technology and Specialties Company, Incorporated,
to Zerbonia, R.A., PES, incorporated. October 1, 1980. Computer
Runs to Simulate the Absorber/Stripper Columns.
15. Telecon. Bjorness, R.A., Metex Process Equipment Corporation,
with Berard, R.E., PES, Incorporated. September 15, 1980. Cost
data for binary absorption columns of varying parameters.
8-22
-------
16. Telecon. McCallister, Bill, Vulcan Manufacturing Company with
Berard, R.E., PES, Incorporated. September 10, 1980. Cost data
for binary absorption columns of varying parameters.
17. Telecon. Breeding, Larry, Glitsch, Incorporated, with Berard,
R.E., PES, Incorporated. September 22, 1980. Cost data for
binary absorption columns of varying parameters.
18. Control Techniques for Volatile Organic Emissions from Stationary
Sources. Environmental Protection Agency/OAQPS, EPA-450/2-78-022.
May 1978. Chapter 3, pp. 24-51, pp. 70-82.
19. Parmele, C.S. et. al. "Vapor-Phase Adsorption Cuts Pollution,
Recovers Solvent" Chemical Engineering. December 31, 1979.
pp. 58-70.
20. Reference 1, pp. 5-39 through 5-50.
21. Cheremisinoff, P.N. and Ellerbusch, Fred. Carbon Adsorption
Handbook. Ann Arbor Science Publishers, Incorporated. 1978.
22. Reference 2, pp. 189-198.
23. Reference 18, pp. 52-69.
24. Vatavk, W.M. and Neveril, R.B. "Estimating Costs of Air Pollution
Control Systems Part III: Estimating the Size and Cost of Pollutant
Capture Hoods." Chemical Engineering. December 1, 1980. pp. 111-115.
25. McDermott, H.J. Handbook of Ventilation for Contaminant Control.
Ann Arbor Science Publishers, Incorporated. 1976. pp. 101-185.
26. Industrial Ventilation-A Manual of Recommended Practice. American
Conference of Governmental Industrial Hygienists. 1980.
27. Vatavuk, W.M. and Neveril, R.B. "Estimating Costs of Air Pollution
Control Systems - Part IV: Estimating the Size and Cost of Ductwork."
Chemical Engineering. December 29, 1980. pp. 71-73.
28. Reference 1, pp. 4-15 through 4-29.
29. Click, C.N. and Moore, D.O. Emission, Process, and Control Technology
Study of. the ABS/SAN, Acrylic Fiber, and NBR Industries; Pullman-Kellogg,
(Report to EPA, Contract No. 68-02-2619, Task No. 6). April 1979.
Appendix D.
30. Economic Impact Assessment for Acrylonitrile. Enviro Control,
Incorporated. (Report to OSHA, Contract Mo. J-9-F-6-0229, Task 3).
February 21, 1978.
31. Reference 1, pp. 4-47 through 4-66.
8-23
-------
32. Letter and attachments from Sonntag, D.F., Amcec Corporation, to
Zerbonia, R., PES, Inc. December 4, 1981. Budgetary proposals
for the supply and installation of solvent recovery systems.
33. Telecon. Quade, Jack, DCI Corporation, with Gladding, D., PES,
Inc. October 6, 1981. Preliminary cost figures for a carbon
adsorption solvent recovery system.
34. Letter and attachments from Davis, W.L., Nuclear Consulting
Services, Inc., to R. Zerbonia, PES, Inc. November 13, 1981,
Budgetary proposals for the supply and installation of solvent
recovery (carbon adsorption) systems.
35. Letter from Detjen, E.P., VARA International, Inc., to Gladding,
D.. PES, Inc. October 29, 1981. Quoted budget prices for
(3) carbon adsorption solvent recovery systems.
36. Telecon. Shaw, Nathan, VIC Manufacturing Company, with Gladding,
D., PES, Inc. October 8, 1981. Preliminary costs for carbon
adsorption solvent recovery systems.
37. Telecon. Spencer, R., Raysoly, Inc., with Gladding, D. PES, Inc.
October 1981. Preliminary costs for carbon adsorption solvent
recovery systems.
38. Letter from Hoi den, J.T., Sutcliffe Speakman, Inc., to Gladding,
D., PES, Inc. December 24, 1981. Budget costs for three solvent
recovery systems.
39. Letter from Pullen, J.C., Celanese Fibers Company, to National
Air Pollution Control Techniques Advisory Committee. September 8,
1981. Proposed NSPS for synthetic fiber production facilities.
40. Report of meeting with Pullen, J.C., Celanese Fibers Company, and
EPA/PES synthetic fibers NSPS; project team. December 3, 1981.
Technical and economic issues.
41. Statement from Ritchie, Tom, Tennessee Eastman Company, to National
Air Pollution Control Techniques Advisory Committee. September 22,
1981. Proposed NSPS for synthetic fibers production facilities.
42. Report of meeting with Vaughn McCoy, et.al., Tennessee Eastman
Company,.and EPA/PES synthetic fibers NSPS project team.
December 1, 1981. Technical and economic issues.
43. Statement from Earnhart, C.R., DuPont Company, to National Air
Pollution Control Techniques Advisory Committee. September 22,
1981. Proposed NSPS for synthetic fibers production facilities.
44. Report of meeting with Earnhart, C.R., DuPont Company, and EPA/PES
synthetic fibers NSPS project team. November 1981. Technical and
economic issues.
8-24
-------
45. "Thermal Incinerator Performance for NSPS", EPA Memorandum from
D. Mascone to J. Farmer, EPA/CPB, June 11, 1980 and Addendum July
22, 1980.
46. Reference 1.
47. Reference 18.
48. Report of Fuel Requirements, Capital Cost and Operating Expense
for Catalytic and Thermal Afterburners, CE Air Preheater Industrial
Gas Cleaning Institute, Stamford, Conn. EPA Report No.
EPA-450/3-76-031, Setpember 1976.
8-25
-------
-------
9.0 ECONOMIC IMPACT
9.1 INDUSTRY CHARACTERIZATION
9.1.1 Industry Overview
Manmade fibers are of two types: cellulosic, and nonce!lulosic
or synthetic. Data on the production of cellulosic fibers are classified
by the U.S. Department of Commerce in Standard Industrial Classification
(SIC) code 2823, Cellulosic Manmade Fibers. Data on the production of
noncellulosic fibers are classified in SIC 2824, Synthetic Organic
Fibers, Except Cellulosic. Cellulosic fibers are known generically as
cellulose acetate, cellulose triacetate, and rayon.. They are produced
from cellulose, the fibrous substance in plants, especially that
derived from spruce and other soft woods. Most noncellulosic fibers
are polyester, nylon, acrylic, modacrylic, or polyolefin. The feedstocks
for these fibers are polymerized petroleum derivatives. The three
types of cellulosic fibers, together with these five types of noncel-
lulosic fibers* currently comprise approximately 99 percent of manmade
fiber production.
The first manmade fiber manufactured in the United States was
rayon in 1910. By 1930, U.S. production of rayon, acetate, rubber,
glass, nylon, and vinyon supplied 10 percent of the fibers used by
domestic textile mills. Commercial production of saran (1941), metallic
(1946), modacrylic (1949), acrylic (1950), polyester (1953), triacetate
(1954), spandex (1959), aramid (1961), and olefin (1961) fibers followed.
By 1979 manmade fibers comprised 75 percent (4,413.8 gigagrams*) of
domestic mill consumption. The use of cotton fiber by U.S. mills
declined from 81 percent to 24 percent over the period 1940-1979; the
use of wool declined from 8 percent to less than 1 percent.
*0ne gigagram equals 1,000 megagrams or 2,207 x 10 pounds.
9-1
-------
The most significant growth in the manmade fibers industry occurred
between World War II and the 1974-75 recession. Historical production
data by fiber type are presented in Table 9-1. Data for 1979 are
presented in absolute and percentage terms to illustrate the relative
importance of each fiber type by quantity of production. Table 9-2
provides quantity of production and value of shipments data by fiber
type for 1977, the most recent year for which value of shipments data
are available. Nylon fiber prices have historically exceeded polyester
fiber prices, causing an incongruity in percentage.of production and
percentage of value data.
9.1.1.1 Role of the Synthetic Fibers Industry in the U.S.. Economy.
The shares of 6NP, employment, and new capital expenditures contributed
by the manmade fibers industry to the national economy provide a
measure of the industry's significance. The most recent data available
to calculate these shares are published by the U.S. Department of
Commerce. Industry data were .obtained by summing the relevant variables
from SIC 2823, Cellulosic Manmade Fibers, and SIC 2824, Synthetic
Organic Fibers, Except Cellulosic, from the 1977 Census of Manufactures.
Domestic economy aggregates were obtained from the Survey of Current
Business.
In 1977, the manmade fibers industry supplied 0.17 of 1 percent
of GNP and 0.1 of 1 percent of total employment. New capital expenditures
by the industry were 0.27 of 1.percent of expenditures on new plant
and equipment by all industries|that year.
These ratios.underestimate the overall significance of manmade
fibers in the economy. As intermediate products, the fibers have
important interindustry linkages. They supply approximately three-fourths
of the fiber (by weight) used by domestic textile mills, which in turn
supply apparel, home-furnishings, and industrial markets. Most types
of manmade fibers have other end uses as well. For example, about
half of the production of cellulose acetate is consumed as cigarette
filtration tow. Nylon fibers are used in air hoses, racket strings,
ropes and nets, tire cord, and thread. Olefin fibers are used to
produce nonwoven felts, ropes and cordage, and sewing thread. Rayon
has applications in medical and surgical products (it is no longer
9-2
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used in the production of tire cord). Modacrylics are used to produce
filters, paint rollers, and wigs, in addition to their more prevalent
use in textiles manufacture.
Some manmade fibers such as aramid and vinyon are consumed entirely
by markets other than the textile industry. Aramid fibers are used to
produce tires, ropes and cables, mechanical rubber goods (such as
gaskets) and structural supports for aircraft and boats. Vinyon
fibers are used primarily by industries as a bonding agent for nonwoven
fabrics and products. None of the manmade fibers has any significant
final (as opposed to intermediate) demand.
The manufacture of manmade fibers consumes intermediate goods
produced by other industries, most significantly the petrochemical and
organic chemicals industry. Data on the most important materials used
by the nonce!lulosic and cellulosic fibers industries are provided in
the 1977 Census of Manufactures. Principal material inputs include
synthetic organic chemicals (especially acetic anhydride, acrylates
and methacrylates, acrylonitrile and glycols), inorganic chemicals
(especially sodium hydroxide and sulphuric acid), plastic resins
(especially polypropylene and nylon resins), liquified petroleum and
refinery gases (ethane and ethylene, propane and propylene, butane,
butylene, and isobutane), natural gas, and paper and paperboard containers.
Producers of cellulosic fibers additionally purchase a significant
amount of wood pulp.
9.1.1.2 The Synthetic Fibers of Interest. Fiber polymer is
extruded through three major processes: melt spinning, wet spinning,
(including reaction spinning) and dry spinning.* In wet and dry
spinning, the fiber polymer must be dissolved in a solvent to produce
an extrudable solution. The principal fibers produced by wet or dry
spinning are acrylics, modacrylics, and all cellulosics. The solvents
used to dissolve the fiber polymers are of two generic types, volatile
organic compounds (VOCs) and aqueous salts. The use of VOCs results
in fugitive emissions of the hazardous chemicals along the process
*A more detailed description of the production processes for each of
the manmade fibers is contained in Chapter 3.
9-5
-------
line. Approximately 77 percent of current production capacity ' for
O
acrylic and modacrylic fibers and all production capacity for cellulose
acetate and triacetate fibers use volatile organic solvents.
Nylon, polyster, and olefin fibers are produced by melt spinning,
which uses heat rather than solvent to melt the fiber polymer for
extrusion. Melt spinning can be used for these fibers because heat
does not degrade the polymers. Because no solvent is needed, emissions
of volatile organic solvents do not occur.
Wet spinning (but not including reaction spinning) and dry spinning,
which use volatile organic chemicals as solvents, are the production
processes for which the EPA recommends further control of VOC emissions.
Maninade fibers falling under these proposed New Source Performance
Standards (NSPS) include cellulose acetate and triacetate, acrylic and
modacrylic, and some specialty fibers such as vinyon that are produced
in relatively small amounts. Although some spandex fibers are produced
by dry spinning, production of this fiber will not be affected by the
NSPS because these plants already meet the recommended levels of
emission control. Rayon fibers are currently produced by the viscose
process, which is a significant source of carbon disulfide and hydrogen
sulfide emissions. However, the EPA was unable to identify control
technology that would result in emission reductions beyond existing
control levels. Furthermore, industry sources report that in all
likelihood there will be no further expansion of viscose rayon capacity.
New nonviscose processes, which do not require the use of sulfur-containing
compounds are being developed, and it appears that producers of rayon
will not increase capacity until a nonviscose process can be implemented.
Viscose rayon processes have therefore been excluded from the source
category subject to the proposed NSPS.
Model plants reflecting new capacity in the acrylics and modacrylics
industry and the cellulose acetate industry were constructed by the
EPA. Costs for the model plants^were estimated for three alternative
levels of VOC control. A profile of each of these two industries is
provided as the first step in the economic analysis.
9-6
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9.1.2 Acrylic and Modacrylic Fibers ;
9.1.2.1 Production
9.1.2.1.1 Product description. Acrylic and modacrylic fibers
are noncellulosic (synthetic) fibers produced from the polymer polyacryloni-
trile. Polyacrylonitrile is made from acrylonitrile, a propylene and
ammonia derivative. Acrylic fibers are defined by the U.S. Federal
Trade Commission as "manufactured fiber in which the fiber-forming
substance is any long chain synthetic polymer composed of at least
Q
85 percent by weight of acrylonitrile units." The remaining 15 percent
or less of the fiber consists of comonomers, generally acrylates,
methacrylates, or vinyl monomers. Modacrylic fibers are defined as
formed from a polymer composed of "less than 85 percent but at least
35 percent by weight of acrylonitrile units, except fibers qualifying
as lastrile or anidex." Modacrylic fibers are made from copolymers
consisting of polyacrylonitrile and other materials such as vinylidene
chloride, vinyl chloride or vinylidene dicyanide.
9.1.2.1.2 Production technology.* Acrylonitrile is converted
into fiber polymer through suspension polymerization or solution
polymerization. All acrylic fibers and approximately half of modacrylic
fibers domestically produced are manufactured through suspension
polymerization.
In suspension polymerization acrylonitrile and comonomers are
polymerized in the presence of a catalyst. Insoluble beads of polyacryloni-
trile polymer are formed that must be dissolved in a solvent to produce
an extrudable solution. Monomers are recovered from the filtration
and washing steps and recycled to the polymerization reactors.
In solution polymerization, acrylonitrile and comonomers are
dissolved in either an organic solvent such as dimethylformamide .
(DMF), dimethylacetamide (DMAc) or acetone, or in a concentrated
aqueous solution of sodium thiocyanate (NaSCN) or zinc chloride (ZnCl2).
A catalyst is added to initiate the polymerization reaction. The
polyacrylonitrile formed is soluble and therefore extrudable. The
*A11 information on production processes has been taken from Chapter 3.
9-7
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filtration, washing, drying, grinding, and redissolving steps that
follow suspension polymerization are avoided.
After polymerization, the [solution is extruded through spinnerets
to form filaments. During the extrusion process, the solvent in which
the polyacrylonitrile was dissolved is removed. The polymer resolidifies,
forming fibers. Approximately |55 percent of domestic acrylic fibers
and 30 percent of domestic modacrylic fibers are produced by wet
spinning; the remainder are produced by dry spinning.
In wet spinning, the solution is extruded into a spinning bath
containing solvent and water. The diffusion of solvent from the
filament to the bath, and the diffusion of water to the filaments
results in a swollen gel filament that must be densified in
post-treatment of the fibers.
In dry spinning, the polyacrylonitrile in solvent is extruded
through a spinneret into a column of hot inert gas. Acetone and DMF
are the preferred solvents for polymer solutions that are dry spun.
As the solvent evaporates, the filaments solidify. The solvent is
condensed in a solvent recovery section and recycled to the dissolving
step. Both wet- and dry-spun fibers require washing, drawing, finishing,
crimping, drying, stapling, and packing.
Regardless of the polymerization or extrusion process, solvent is
captured and reused. Volatile organic solvent is captured by precipitation
or enclosures, scrubbed, and returned to the polymerization, dissolving
and spinning steps. Aqueous salt solvents (used only in wet spinning)
are recovered by precipitating the solvent from the used solvent bath
in a captive wastewater treatment facility.
Domestic acrylic and rnodacrylic fiber producers perform at least
polymerization of the input acrylonitrile. Only two producers purchase
acrylonitrile; the rest manufacture it from captive or purchased
propylene and ammonia. The producers spin, cut, crimp, and bale the
fiber. None of the producers are integrated forward to the manufacture
of textiles.
For the most part, the production technology is well established;
however, variations exist. As noted previously, either suspension or
:9-8
-------
solution polymerization may be used. Polymerization may be either
batch mode or continuous regardless of the polymerization process.
The solvent used to dissolve the polymer.may be either a volatile
organic compound or an aqueous salt. The production technology is
available for sale by the producers.
9.1.2.1.3 Production history. Modacrylic fibers were first
commercially produced in the United States in 1949 by Union Carbide
Corporation. Acrylic fibers in the form of continuous monofilarnent
yarns were first produced in 1950 by E. I. du Pont de Nemours & Company,
Inc. Du Pont began producing acrylic staple in 1952, and discontinued
production of acrylic ^onofilament yarn in 1956. Only small amounts
have been produced since that time. Data on annual domestic production
of acrylics and modacrylics for the period 1960-1980 are presented in
Table 9-3. Production of acrylic and modacrylic continuous filament
yarn has never been significant, and therefore data are not available.
Acrylic continuous filament yarn production from 1950 to 1956 and 1963
to 1965, and modacrylic yarn production from 1948 to 1954, is believed
to have totaled little more than one fifth a gigagram (less than one
13
half million pounds) annually. Between 1960 and 1973, output increased
from 61.5 to 336.2 gigagrams, but it declined in 1974 and 1975, falling
to 237.6 gigagrams. Since 1975, production has steadily increased,
rising to 353.4 gigagrams in 1980. The decline in output from 1973 to
1975 is explained by higher input (propylene) prices and decreased
demand due to the worldwide recession occurring in those years.
9.1.2.1.4 Role in U.S. economy. The adrylics and modacrylics
fiber industry contributed 0.0001 of 1 percent of total GNP, 0.006 of
1 percent of total employment, and 0.003 of 1 percent of expenditures
on new plant and equipment by all industries in 1977.
These ratios are not mathematically significant from zero given
the accuracy of the data from which they were calculated. As a measure
of the importance of the acrylic and modacrylics industry to the
aggregate economy, these ratios are misleading. Because acrylic and
modacrylic fibers are intermediate products, the industry functions as
both a demander of outputs of certain industries and a supplier of
inputs to other industries.
9-9
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TABLE 9-3. DOMESTIC PRODUCTION OF ACRYLIC AND
MODACRYLIC STAPLE, TOW AND FIBERFILL
(EXCLUDING WASTE)11 12
1960
1961
1962
1963
1964
1965
1966
1967
1968
1969
1970
1971
1972
1973
1974
1975
1976
1977
1978
1979
1980
Production
(gigagrams)
61.5
63.5
77.0
95.0
130. 3
166.9
159.9
180.2
236.0
241.4
222.8
247.0
283.5
336.2
285,9
237.6
281.3
321.1
328.7
344.8
353.4
(million
pounds)
135.7
140.1
170.0 ,
209.7
287.7
368.4
352.9 ,
397.7
521.0
533.0
491.9
545.2
625.9
742.1
631.2
524.6
621.0
708.8
725.7
761.1
779.2
9-10
-------
The most significant purchases by acrylic and modacrylic fiber
producers are acrylonitrile or the inputs to its production (propylene
and ammonia) and solvents such as acetone,\ DMAc, DMF, and aqueous
salts. The most significant market for acrylic and modacrylic fibers
is the textile industry, specifically knitting and weaving mills, and
carpet and rug manufacturers. Textiles produced from acrylic and
modacrylic fibers in turn supply manufacturers of apparel, blankets,
and draperies and curtains. Acrylic and modacrylic fibers compete
primarily with the wool industry in supplying the apparel market and
the nylon and polyester industries in supplying the home-furnishings
market.
9.1.2.1.5 Factors of production. Acrylonitrile, the basic raw
material of acrylic and modacrylic fiber production, is produced by
reacting a mixture of propylene, ammonia, and air in the presence of a
catalyst. Acrylonitrile is used as an intermediate in the production
of acrylic and modacrylic fibers, acrylonitrile-butadiene-styrene
(ABS) resins, styrene-acrylonitrile (SAN) resins, nitrile elastomers,
adiponitrile (a raw material in Nylon 66), and acrylamide monomers and
polymers.
In 1979, approximately 39 percent of the acrylonitrile produced
domestically was used in the manufacture of acrylic and modacrylic
fibers. Another 17 percent was used to produce resins such as ABS,
3 percent was used in nitrile elastomers, and 20 percent was used in
miscellaneous applications including the manufacture of intermediates
(such as adiponitrile) for the production of nylon. The residual
14
21 percent was exported.
Currently, four firms manufacture acrylonitrile; three are also
producers of acrylic and modacrylic fibers. Table 9-4 lists these
producers, their plant locations, and plant capacities as of January 1,
1981. Two other firms have discontinued production of acrylonitrile.
Union Carbide produced acrylonitrile between 1954 and 1966 in a
small-scale operation in Institute, West Virginia. B. F. Goodrich
produced acrylonitrile in a pilot plant at the Avon Lake Technological
Center in the 1950s and in Calvert City, Kentucky, from 1954 to 1972.
Both companies discontinued manufacture of the product because their
9-11
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plant capacities were too small to be competitive with the larger
producers.
As indicated by Table 9-4, Monsanto Company recently expanded its
acrylonitrile capacity by 50 percent. Two other acrylonitrile producers
are in the process of constructing new plant capacity. Du Pont has an
acrylonitrile plant under construction at Victoria, Texas, that is to
be completed by the fourth quarter of 1982. The new plant is intended
to replace existing capacity. Standard Oil Company of Ohio's subsidiary,
Vistron Corporation, has additional capacity of 181 gigagrams per year
under construction at Green Lake, Texas. The plant is expected to be
completed in the fourth quarter of 1981.
Both Eastman Kodak Company (Tennessee Eastman) and Monsanto are
increasing propylene production capacity. Eastman Kodak began adding
50 percent to its current capacity of 181 gigagrams per year in 1981;
Monsanto has recently doubled its current capacity of 249 gigagrams
per year in a joint venture with Conoco, Inc.
Production of modacrylic fibers requires chlorinated vinyl
comonomers in addition to acrylonitrile as inputs to polymerization.
None of the modacrylic fiber producers manufactures its own comonomers.
The other raw materials used in acrylic and modacrylic fiber
production are primarily solvent and finish. The solvents used by
domestic producers of acrylic fibers are aqueous NaSCN and ZnClg, DMF
and DMAc. Solvents used by domestic producers of modacrylic fibers
are DMF, DMAc, and acetone.
19
Du Pont manufactures both DMAc and DMF. The firm utilizes DMF
in its production of both acrylic and modacrylic fibers. Monsanto
purchases DMAc for its production of the two fibers. American Cyanamid
Company and Badische Corporation produce only acrylic fibers; they.use
an aqueous salt (NaSCN) and zinc chloride, respectively, for solvent.
Tennessee Eastman, which produces only modacrylic noncellulosic fibers,
uses captively produced acetone as a solvent for these fibers and for
its cellulose acetate textile fibers and cigarette filtration tow.
The final raw material used in the production of acrylic and
modacrylic fibers is finish. The cost and availability of finish were
determined by the EPA to have negligible impacts on production.
9-13
-------
The 1977 Census of Manufactures reports that 5,700 persons are
employed in plants primarily producing acrylic and modacrylic fibers.*
Production workers involved in the polymerization and spinning steps
are semiskilled and are trained on the job for 1 year. There are
usually two production workers per spinning line; acrylic and modacrylic
fiber production is capital rather than labor intensive.
Producers of acrylic and modacrylic fibers can easily switch
between production of the two fibers. Although raw materials differ—
production of modacrylic fiber requires a copolymer of acrylonitrile
and a chlorinated vinyl comonomer, and production of acrylic fiber
requires a polyacrylonitrile polymer—both fibers are produced with
solvents such as DMF, DMAc, or acetone. Processes for dissolving the
polymer in solvent and spinning the fibers are interchangeable between
the two types of fiber; therefore, the same capital machinery .can be
used for both. Indeed, Eastman Kodak is reported to use the same
polymerization, solution prepa'ration, and spinning equipment to manufacture
both modacrylic and cellulose'acetate fibers; hence the use of acetone
as the solvent for both fiber types. Polymerization and extrusion
facilities are general to all fiber types. Machinery for texturizing
and cutting tow is specific to staple production; machinery for spinning
yarns from staple fibers is specific to yarn production.
The relative amounts of acrylonitrile and comonomer, and the
relative amounts of polymer and ; sol vent, used to produce acrylic and
modacrylic fibers may be varied, yielding fibers with distinct
characteristics. For example, the chlorinated vinyl comonomers used
in modacrylic fiber production may be used to produce flame-resistant
fibers. The relative amounts of polymer and solvent employed in wet
spinning are varied according to the denier of fiber being manufactured.
There does not appear to be much potential for the substitution of
capital for labor in the polymerization and spinning processes of
*This employment figure is subject to error in both directions due to
the Census method of classifying plants by primary product. First, the
figure excludes employment in plants that manufacture acrylic and mod-
acrylic fibers as a secondary product. Second, the figure includes
employment that is not related !to acrylic or modacrylic production in
plants that manufacture acrylic or modacrylic fibers as a primary product,
9-14
-------
acrylic and modacrylic fibers. Substitution of capital equipment for
solvent is evidenced by the increased recovery rate of solvent resulting
from emissions control equipment.
9.1.2.2 Supply Conditions. The most recent data for domestic
shipments of acrylic and modacrylic staple, tow, and waste fiber dis-
aggregated by apparel, home-furnishings, and industrial end uses
indicate that apparel consumed 68 percent of acrylic and modacrylic
9fi
fibers in 1975. Acrylic and modacrylic fibers were primarily used
to produce craft yarns; sweaters; pile fabrics; top-type fabrics for
shirts, blouses, and light-weight dresses; anklets and socks; and
bottom-type fabrics for pants, sportswear, and tailored clothing. In
the home-furnishings market, which consumed almost 27 percent of
acrylic and modacrylic staple, tow, and waste fibers, the primary end
uses were carpets, rugs, and blankets. The residual industrial uses
were primarily doll hair and fabric for toys, fiberfill, and stuffing.
Table 9-5 provides a breakdown of domestic shipments .by acrylic and
modacrylic staple and tow for the years 1970-1975. The primary distinctions
of modacrylic fibers compared to acrylic fibers are that they duplicate
more closely the feel and appearance of natural fur, they dye more
easily and, due to the comonomers present in the polymer, they may be
modified to be flame resistant. A more detailed analysis of the end
uses for acrylic and modacrylic fibers is provided in Section 9.1.2.3.
Acrylic and modacrylic fabrics are produced from high-bulked
yarns spun from staple. The yarns are combinations of high- and
low-shrinkage staple. Applying heat to the yarn causes the high-shrinkage
staple to squeeze the low-shrinkage staple to the surface, making the
yarn bulky, fluffy, and soft. Mechanically crimping the staple fiber
gives the yarn even more bulk. Therefore, the demand is for acrylic
and modacrylic staple fiber, and production of continuous monofilament
yarn has been discontinued.
Table 9-6 illustrates the relative magnitude of production of
acrylic and modacrylic fibers. The table indicates that after the
first few years, relative production stabilized at a bit more than
90 percent acrylic fiber.
9-15
-------
TABLE 9-5. TOTAL SHIPMENTS OF ACRYLIC
AND MODACRYLIC STAPLE AND TOW21
Cgigagrams)
Year
1970
1971
1972
1973
1974
1975
Acrylic
201.8
223.4
266.3
316.2
246.4
233.4
Modacry 1 i c
17.8
16.9
19.1
30.0
23.1
17.4
Totala
219.6
240, 2
285.4
346.2
269.5
250.8
Excludes waste; includes domestic shipments and exports.
9-16
-------
TABLE 9-6. DOMESTIC PRODUCTION OF
ACRYLIC AND MODACRYLIC BY FIBER TYPE12 13
(gigagrams)
1948
1949
1950
1951
1952
1953
1954
1955
1956
1957
1958
1959
1960
1961
1962
1963
1964
1965
1966
1967
1968
1969
1970
1971
1972
1973
1974
1975
1976
1977
1978
1979
1980
Aery 1 i c
0.0
. 0.0
F0.5
0.5
5.0
6.8
11.8
26.3
32.2
43.9
45.8
58.9
56.6
59.3
71.1
87.4
119.6
153.1
144.5
163.1
215.2
222.0
205.2
229.7
264.6
305.3
N/A
N/A
N/A
N/A
N/A
N/A
N/A
Modacrylic
FO.l
FO.l
0.5
0.9
0.9
0.9
0.9
1.8
2.3
3.6
3.2
4.5
5.0
4.1
5.9
7.7
10.9
14.0
15.4
17.2
20.8
19.5
17.7
17.2
19.0
30.8
N/A
N/A
N/A
N/A
N/A
N/A
N/A
Total
FO.l
FO.l
Fl.O
1.5
5.8
7.7
12.7
28.0
34.3
47.6
49.2
63.2
61.5
63.5
77.0
95.0
130.3
166.9
159.9
180.2
236.0
241.4
222.8
247.0
283.5
336.2
285.9
237.6
281.3
321.1
328.7
344.8
353.4
Acrylic as
percent of total
0
0
F50.0
33.3
86.2
88.3
92.9
93.9
93.9
92.2
93.1
93.2
92.0
93.4
• 92.3
92.0
91.8
91.7
90.4
90.5
91.2
92.0
92.1
93.0
93.3
90.8
-
-
-
-
-
-
—
9-17
-------
9.1.2.2.1 Domestic producers. The domestic producers of acrylic
and modacrylic fibers are listed in Table 9-7. Plant-specific capacity
data for 1970 and 1974-1981 are also presented. Minor additions; to
capacity are evidence of improvements in the efficiency of capital
machinery. The only plant closure occurred in June 1975, when Union
Carbide discontinued modacrylic fiber production in Charleston, West
Virginia. The capital equipment of the plant was dismantled; the
capital machinery specific to spinning fibers was scrapped by Union
Carbide as no buyer could be found. Union Carbide's plant had an
annual capacity of 10 gigagrams (22 million pounds) of fiber, which
was consumed in all modacrylic fiber markets and was particularly
important in the deep-pile fabrics, drapery, scatter-rug, and hairpiece
markets.25 Union Carbide was never able to generate sufficient demand
for this fiber to result in a profitable operation.
Two of the producers, American Cyanamid and Badische Corporation,
will not be affected by the proposed NSPS because neither uses a
solvent that is a volatile organic compound. American Cyanamid uses
an aqueous salt for solvent; Badische Corporation uses zinc chloride.
In 1977, shipments by all domestic producers of acrylic and
modacrylic fibers (yarn, staple, tow and waste) were valued at
$495.8 million by the Bureau of the Census. Shipments by quantity
were estimated to be 336.3 gigagrams (741.4 million pounds). The
implied average producer price is therefore $1.48 per kilogram
($0.67 per pound). Shipments of acrylic and modacrylic staple were
estimated to have a value of $370.2 million and to total 259.1 gigagrams
(571.3 million pounds), for an implied producer price of $1.43 per
kilogram ($0.65 per pound). The:residual shipments of 77.2 gigagrams
(170.2 million pounds), valued at $125.6 million, can be assumed to
consist of multifilament yarn, tow, and salable waste. Shipments of
monofilament yarn in 1977 were estimated by the Bureau of the Census
to be zero; this is consistent with data collected by the Textile
oc
Economics Bureau.
The relatively low value-to-weight ratio of the fibers, plus
their bulkiness, tends to make shipping cost an important consideration
in the purchase decision of a fiber user. As a consequence, a fiber
9-18
-------
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9-19
-------
producer who is closely located to his customers has a competitive
advantage. One would expect, therefore, that fiber producers would
locate near fiber-consuming industries, and this appears to be the
case. Acrylic and modacrylic fiber producers are concentrated in the
southeastern United States, near the center of the domestic textile
manufacturing industry.
9.1.2.2.2 Industry structure and capacity. Table 9-8 illustrates
the end-use markets that the various producers supplied in 1975, the
most current year for which such data are available. All producers
compete in the market for textilie staple and tow (for both apparel and
home furnishings). American Cyahamid and Monsanto are the two competitors
in the market for acrylic fiber for carpet. End use of acrylic and
modacrylic staple and tow in textile manufacture was approximately
72 percent of all end uses in 1975. Carpet manufacture accounted for
27
about 27 percent of end use.
Many qualitative data indicate that the acrylic and modacrylic
staple and tow produced by the various companies are differentiated
and have segmented end uses within apparel, home-furnishings, and
industrial segments of the market. However, no detailed quantitative
data are available to confirm or deny this implication that the fibers
produced by the various companies are not substitutable for one another.
All manufacturers of acrylic and modacrylic fibers have captive
polymerization facilities. Eastman Kodak and Badische purchase acrylonit-
rile for polymerization; the other three manufacturers make acrylonitrile.
American Cyanamid produces acrylonitrile from purchased propylene and
captive ammonia. Monsanto has captive supplies of both propylene and
ammonia. Du Pont produces acrylonitrile from captive supplies and
supplemental purchases of propylene and ammonia. None of the modacrylic-
fiber manufacturers (Du Pont, Eastman, Monsanto) produces its own
OQ
vinyl chloride or vinylidene chloride comonomers.
American Cyanamid manufactures and sells products in five major
areas: agricultural chemicals including fertilizers, pesticides,
animal feed, and veterinary products; consumer toiletries, hair
preparations, and perfumes; Pharmaceuticals; industrial and specialty
OQ
chemicals; and Formica construction products. American Cyanamid
9-20
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9-21
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31
does not manufacture textiles from its acrylic fibers, but sells the
fibers as an intermediate good (staple and tow forms) to textile
manufacturers. The firm does manufacture acrylic sheet and acrylic
30
molding compounds.
Eastman Kodak is the world's largest producer of photographic
products, manufacturing amateur and professional films and equipment
and related supplies. In addition to synthetic textile fibers (acetate,
modacrylic, and polyester), Eastman Kodak produces plastics and chemicals.
The company does not manufacture textile products from its fibers.
Du Pont is the largest domestic chemical producer, manufacturing
nylon, polyester, acrylic and specialty fibers; chemicals and pigments;
elastomers, films, engineering resins and other plastic products; and
medical, printing, electronic, explosives and agricultural specialty
32
products. Du Pont produces aramid, nylon, olefin, polyester, spandex
33
and Teflon fibers, which are sold directly to textile producers.
The firm also manufactures acrylic finishes and coatings and filled
34
acrylic building products.
Monsanto is the fourth largest producer of chemicals in the
United States. Primary products of the company are herbicides, insecticides,
nitrogen fertilizers, industrial and specialty chemicals, intermediates,
plastics and resins, process controls and electronics, chemical and
35
environmental systems, and nylon and polyester fibers. A producer
of acrylonitrile, Monsanto makes ABS and SAN resins as well as acrylic
and modacrylic fibers. Manmade fibers generated approximately 17 percent
OC
of Monsanto's sales in 1979.
Badische Corporation has been fully owned by BASF-Ag of West
Germany since 1978. Prior to that, the company was partly owned by
BASF and Dow Chemical, under the^name Dow Badische Company.
Table 9r9 indicates the relative importance of fiber sales to
each domestically owned producer of acrylic or modacrylic fibers. It
is evident from the companies that make acrylic and modacrylic fibers
that the industry is a part of the chemical industry. Production of
acrylic and modacrylic fibers is closely linked with the production of
the polymers and solvents used as inputs. The fiber producers sell to
diverse markets, but do not themselves compete in textile, carpet or
other end-use markets.
9-22
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The capacity data for the industry, presented in Table 9-10,
indicate a high degree of concentration. There is a small number of
firms., and currently more than 70 percent of total capacity is owned
by the two largest firms, Du Pont and Monsanto. Further, both the
acrylic and modacrylic segments of the industry are dominated by two
companies. In the case of acrylics, Du Pont and Monsanto operate more
than 70 percent of total capacity; in the case of modacrylicsa Eastman
Kodak and Monsanto operate more than 85 percent of total capacity.
Table 9-11 provides production and production capacity time-series
data for the aggregate domestic acrylic and modacrylic industry.
Growth in capacity was rapid in the years 1960-1974; the compound
annual average rate of growth was nearly 10 percent, compared to a
rate of just less than 1 percent from 1974 to 1980.
Capacity increases were supported by the growth in production
from 1960 through 1973, with only minor and temporary setbacks in 1966
and 1970. A drastic decline in production (some 30 percent) occurred
over the years 1974 and 1975. Since 1976, production has again increased,
although capacity has remained stable. Consequently, by 1980 the
operating rate for the industry was approximately 90 percent. The
data presented in Table 9-6 indicate that most production growth (and
absolute production) has occurred in acrylic rather than modacrylic
fibers. All production is in staple and tow forms of fiber; the
production of waste fiber (approximately 5 percent) is ancillary.
9.1.2.2.3 Industry performance. Table 9-12 contains annual
financial data for the domestically owned producers of acrylic and
modacrylic fibers for the years :1977 through 1979. It is evident that
net sales for the four companies have kept pace with, and probably
exceeded, the rate of inflation over the period. The earnings before
interest and taxes of Du Pont and Eastman Kodak have also kept pace
with inflation. Hith the exception of Du Pont, all companies increased
their nominal levels of long-term debt over the period; however it is
not evident that any firms increased real levels of long-term debt.
All four of the companies appear to be financially sound overall. The
caveat must be added that these [aggregate financial data shed no light
on the financial status of the mpdacrylic- and acrylic-producing
9-24
-------
TABLE 9-10. DOMESTIC PRODUCERS OF ACRYLIC
AND MODACRYLIC FIBERS RANKED BY CAPACITY, 197510
Company
E. I. du Pont de Nemours &
Co. , Inc.
Monsanto Co.
American Cyanamid Co.
Dow Badische Co.a
Eastman Kodak Co.
Company
E. I. du Pont de Nemours &
Co. , Inc.
Monsanto Co.
American Cyanamid Co.
Dow Badische Co.a
Company
Eastman Kodak Co.
Monsanto Co.
E. I. du Pont de Nemours &
Co. , Inc.
Rank
1,2
1,2
3
4
5
Rank
1
2
3
4
Rank
1
2
3
Percent of
total acrylic and
modacrylic capacity
38.0
32:4
15.6
9.0
5.0
Percent of
acrylic capacity
40.6
32.3
17.2
9.9
Percent of
modacrylic capacity
53.3
33.3
13.3
Cumulative
percent
36.2
70.4
86.0
95.0
100.0
Cumulative
percent
40.6
72.9
90.1
100.0
Cumulative
percent
53.3
86.6
99.9
Dow Badische Co. was a joint venture of Dow Chemical Company (U.
Overzee, N.V. In June 1978, the company was sold to BASF-Ag of
was later renamed Badische Corp.
S.A.) and BASF
W. Germany and
9-25
-------
TABLE 9-11. PRODUCTION AND PRODUCTION CAPACITY OF
ACRYLIC AND MODACRYLIC FIBERS, 1960-198012 3S 39
Year
1960
1961
1962
1963
1964
1965
1966
1967
1968
1969
1970
1971
1972
1973
1974
1975
1976
1977
1978
1979
1980
Capacity9
(gigagrams)
93.8
97.4
103.3
119.1
152.7
202.0
228.8
243.7
278.6
292.2
298.5
316.2
341.6
356.5
373.3
374.6
393.7
393.7
391.8
394.1
394.1
Total
production
(gigagrams)
61.5
63.5
77.0
95.0
130.7
166.9
159.9
180.2
236.0
241.5
222.8
247.0
283.5
336.2
285. 9
237.6
281.3
321.1
328.7
344 . 8
353.4
Capacity
utilization
(percent)
66
65
75
80
86
83
70
74
85 ;
83 :
75
78
83
94
77
63
71
82
84
87
90
November of the year.
9-26
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9-27
-------
divisions of the firms. As shown in Table 9-9, fiber sales by Du Pont
and possibly Monsanto do not appear to have declined in real terms,
but those of Eastman Kodak and American Cyanamid have. Given the
escalating costs of polymer and solvent, this would seem to indicate
that these firms are experiencing declining rates of return for fiber
production. The outlook for capacity increases without prior improvement
in rates of return is bleak.
9-l»2.3 Demand Conditions. The demand for acrylic and modacrylic
fibers is driven by the demand for final products that are several
processing and marketing steps removed from the production of the
fibers themselves. For example, a substantial portion of the demand
for acrylic and modacrylic staple and tow comes from the knitting
mills of the textile industry, these mills, in turn, respond to
consumer demand for sweaters, socks, shirts, etc., as expressed through
retail and wholesale apparel markets.
Textile mills often blend acrylic and modacrylic fibers with
other types of fibers to make textile yarn. The demand for the fibers
is therefore derived from consumer demand for a highly reworked> mixed
fiber product. Once spun into yarn, the fiber is woven into cloth to
be cut and sewn into apparel, linking final consumer demand with the
output of acrylic and modacrylicifibers. The demand for acrylic and
modacrylic fiber used in automobile interiors or household carpeting
depends on consumer demand for automobiles and home construction.
9.1.2.3.1 Fiber end uses. The Textile Economics Bureau conducts
periodic surveys to determine the end uses that support fibers production.
The results of the surveys are reported first in the periodical,
Textile Organon, and then in more comprehensive form every five years
in the Man-Made Fiber Producers' Base Book. The most detailed end-use
data for acrylic and modacrylic fibers published from the surveys
apply to staple and tow shipments. This is expected since staple and
tow have accounted for approximately 95 percent of acrylic and modacrylic
shipments in recent years.
The end-use data may be further partitioned into three general
classes: apparel, household'furnishings, and industrial and other
consumption. Tables 9-13 to 9-15 present time-series data for acrylic
9-28
-------
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9-30
-------
TABLE 9-15. SHIPMENTS OF ACRYLIC AND MODACRYLIC STAPLE AND TOW
BY INDUSTRIAL AND OTHER CONSUMER END USES43
(gigagrams)
End use
1968 1969 1970 1971 1972 1973 1974 1975
Flock
Doll hair, toys, etc.
Fiberfill and stuffing
Felts
Filtration
Bags and bagging
Coated and protective
fabrics
Other industrial and
consumer uses
Total
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9.
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1
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4.3
Other industrial and other consumer uses include narrow woven fabrics,
medical, surgical and sanitary fabrics, transportation upholstery, sewing
thread, paper and tape reinforcing, paint roller covers, wiping cloths,
tobacco shade cloth, and other.
TABLE 9-16. SHIPMENTS OF ACRYLIC AND MODACRYLIC
FIBER WASTE BY END USE44
(gigagrams)
End use
1968 1969 1970 1971 1972 1973 1974 1975
Pile fabrics
Other apparel
Blankets
Needle-punched carpets
Other carpets and rugs
Drapery
Upholstery
Nonwoven structures
Filling and stuffing
Rope, cordage and twine
Other domestic
Total domestic
Exports
Total waste
1.
0.
1.
1.
1.
0
0
0
6.
0.
6.
7
2
5
7
5
7
2
9
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0
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1.4
9.6
1.4
0.5
5.3
1.4
1.2
0
1.2
0
11.0
0.3
11.2
0.3
0
6.7
0.1
1.6
0
1.8
0
10.6
0
10.6
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5.
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2.
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2.
0.
10.
0.
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3
3
2
1
6
2
7
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0
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0
2.0
0
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0
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0
1.
0
8.
0
8.
2
4
1
6
5
5
0
0.5
4.8
0
1.9
0
1.8
0
9.0
0
9.0
9-31
-------
and modacrylic staple and tow shipments to various end uses within
each of these three classes. In 1975, the last year for which fairly
disaggregated end-use data are available, apparel end use accounted
for 71 percent of domestic shipments to domestic processors of fiber.
Home-furnishings end use accounted for 26 percent of such shipments;
the residual was consumed in industrial and other consumer applications,
Within the various apparel categories, the largest end uses were
estimated to be in craft yarns (25.6 percent), sweaters (20.1 percent),
pile fabrics (20.0 percent), anklets and socks (12.6 percent) and
top-type fabrics (12.6 percent). Among home-furnishings end uses,
most of the fiber shipped in 1975 was used in tufted-face .broadloon
rugs (61.0 percent) and blankets (26.9 percent). Doll hair, toys,
etc., accounted for 40.6 percent of industrial use of acrylic and
modacrylic fibers.
These data series illustrate the recent variations and trends in
the end use of acrylics and modacrylics. The fluctuations in the
shipments to apparel end uses appear to reflect changes in style, such
as the popularity of polyester knits in the mid-1970s, and world
events, such as the increased use of sweaters associated with the rise
in energy prices after 1973. Shipments of acrylic and modacrylic for
use in blankets have risen dramatically since 1972-1973, while the use
of acrylic and modacrylic in rugs appears to have fallen off since
1968 due to competition from nylon fibers. Data that distinguish
between acrylic and modacrylic end use are not available.
Shipments of acrylic and modacrylic waste by end use are presented
in Table 9-16. This table shows ithat over the period 1968-1975., the
use of acrylic and modacrylic waste in pile fabrics and needle-punched
carpets was phased out, while its use in blankets (over 52 percent of "
waste shipments in 1975) and filling and stuffing grew considerably.
Time-series data on domestic shipments of acrylic and modacrylic
staple, tow, and waste by the three principal classes of end use and
exports are presented in Table 9-17, As mentioned previously, the
apparel end use dominates acrylic and modacrylic consumption, and most
of the remaining shipments are to the home-furnishings industry.
9^-32
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9-33
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Acrylic and modacrylic fibers can be blended with other fibers
when spun into yarn. Such blending may enhance the characteristics of
other fibers as well as substitute for them. As a result, the market
role of acrylic and modacrylic fibers relative to other fibers is
difficult to establish. Because of the characteristics of acrylics
and modacrylics, they appear to! compete most directly with natural
fibers such as wool or cotton in the sweater, sock and pile-fabric
markets. On the basis of end-use data for bottom-type and top-type
fabrics, acrylic and modacrylic fibers appear to compete also with
natural fibers and polyester. End-use data indicate competition with
nylon and polyester fibers in the carpet market. The data presented
in Table 9-18 show that the role of acrylics and modacrylics in the
staple and tow market declined dramatically relative to that of nylon
and polyester between 1960 and 1975.
In summary, the market for acrylic and modacrylic fibers is both
diverse and driven by consumer demand several steps•removed from
actual fiber production. Shipments of acrylic and modacrylic fibers
are 95 percent staple and tow, most of which is spun and knit into
apparel. Other fibers may either complement or substitute for acrylic
or modacrylic staple and tow, depending on the particular fiber and
end use considered. While it appears that acrylics and modacrylics
have at least maintained their competitive position relative to natural
fibers, they have been losing portions of their apparel and home-
furnishings market to polyester and nylon. Foreign competition in the
acrylic and modacrylic fiber market is indirect, coming principally
from imports of finished consumer goods.
9.1.2.3.2 Foreign trade. Exports of acrylic and modacrylic fiber
staple and tow have grown faster than domestic consumption. Between
1963 and 1980, annual compound growth in exports was 17.9 percent, as
compared with 6.5 percent growth in shipments to domestic processors.
Even so, exports of staple and tow accounted for only 24.1 percent of
all shipments of acrylic and modacrylic staple and tow in 1980.
Exports of waste have been very small or insignificant in recent
years.
9-34
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9-35
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Imports of acrylic and modacrylic fibers, shown in Table 9-19,
have generally declined since the early 1970s. In 1980, staple and
tow imports were 6.0 gigagrams. Of course, fiber produced abroad is
most likely to be imported in the form of finished goods such as
imported clothes. Textile Organon refers to "substantial imports of
finished products, such as neckties, sweaters, blankets, tablecloths,
rugs, hosiery, shirts, suits and dresses, etc., (which) are not included
in the (end-use) survey ...."
9.1.2,4 Projections. Projections of growth for the acrylic and
modacrylic fibers industry contained in published sources vary consid-
erably. Consequently, with a current industry capacity utilization
rate of 90 percent, the various growth projections yield strikingly
different results for projecting dates for capacity additions. The
following paragraphs summarize the projected growth rates contained in
published sources.
Data Resources, Inc., (DRI) in its publication Chemical Review
(Winter 1979) forecast quantity of production of acrylic fibers for
the years 1982, 1985, 1990 and 1995, with a base year of 1978.4/ The
implied average annual growth rates compounded annually are 0.7 percent
through 1982, 5.6 percent in the period 1982-1985, 1.8 percent in
1985-1990, and 1.5 percent from 1990 to 1995. The implied average
annual growth rate (compounded annually) over the period from the base
year to 1990 is 2.3 percent. The capacity shortfalls projected by DRI
(assuming maximum capacity utilization of 92 percent) were 25 gigagrams
(56 million pounds) in 1985, 63 gigagrams (138 million pounds) in
1990, and 96 gigagrams (211 million pounds) in 1995.
DRI also projected growth in domestic consumption for these same
years. The implied average annual growth (compounded annually) for
the period 1978 to 1990 is 3.4 percent. The difference in the projected
i
growth rates for domestic consumption and for production are due to
projected growth rates for imports, exports, and changes in inventory
levels over the period.
As mentioned, 1978 data were the most recent available at the
time URI projected growth rates. The projections are therefore somewhat
dated. In contrast with other projections and in light of the general
9^36
-------
TABLE 9-19. ACRYLIC AND MODACRYLIC FIBER IMPORTS12 3S
(gigagrams)
Year
1964
1965
1966
1967
1968
1969
1970
1971
1972
1973
1974
1975
1976
1977
1978
1979
1980
Staple and tow
6.5
13.0
8.8
15.8
22.3
15.6
12.0
21.8
19.3
19.4
8.8
3.8
7.5
7.4
8.2
5.9
6.0
Waste
1.0
1.5
1.4
1.6
2.2
1.9
2.5
3.7
4.6
4.4
3.1
2.0
2.5
1.6
N/A
N/A
N/A
Total
7.5
14.5
10.2
17.4
24.4
17.5
14.5
25.5
23.9
23.9
11.8
5.8
10.0
8.9
N/A
N/A
N/A
9-37
-------
economic conditions of the years 1979 to 1980, the DRI projectons
somewhat overstate growth in those years.
Chemical and Engineering News (C&EN) in the December 1, 1980,
issue reports that demand for acrylic fibers grew at an average annual
rate of 3.8 percent from 1976 to end-of-the-year 1979, and that growth
in 1980 was comparable. C&EN reports that some acrylic fiber producers
expect growth in demand of 5 percent in 1981. However, some producers
are forecasting "long-term growth for acrylic fibers at no more than
48
1 percent per year." These growth projections are less than satisfactory
because they are difficult to interpret. The bases and sources for
the projections are not clear, making it difficult to determine their
reliability and appropriateness.
Textile Industries in February 1979 forecast rates of growth in
domestic mill fiber consumption (domestic shipments plus imports) for
40
cellulosic, noncellulosic and synthetic fibers. The original sources
for the data were the Textile Economics Bureau and International
Research Associates. Growth in domestic mill consumption of all
fibers is projected to result from reduced imports, increased exports
and increasing population. For acrylic and modacrylic fibers, the
projected average annual rates of growth in domestic mill consumption
are 1.9 percent through 1982 and 1.6 percent in the period 1982-1987.
These projections do not specifically address projected growth in
production; however, the qualitative statement that imports of fiber.
will most likely decline suggests that these growth rates do not
overestimate comcomitant growth in production.
The final published source of data for projected growth in the
acrylics and modacrylics fiber industry is the January 1981 issue of
50
Textile Organon. The Organon summarizes a speech by Dr. David K.
Barnes of Du Pont that presented Du Font's forecasts of growth in
domestic consumption of various noncellulosic synthetic fibers,.
Domestic consumption of acrylic fibers was forecast to grow at an
average annual rate of 2.7 .percent during the period 1979 to 1985.
Again, this forecast is not equivalent to a forecast for growth in
domestic production because growth or decline in import and export
markets is not addressed. However, imports of acrylic and modtitcrylic
9-38
-------
fibers have generally declined since the early 1970s, so that it would
not appear that projected growth of 2.7 percent in domestic mill
consumption would overestimate growth in domestic production.
To supplement these forecasts from published sources, EPA estimated
regression equations using time-series data on domestic production of
acrylic and modacrylic fibers. These regression equations provided
"in-house" projections that were additional indicators of likely
growth in domestic production of acrylic and modacrylic fibers. The
annual production data used to estimate the regression equations were
collected by the Textile Economics Bureau for the years 1960-1979.
The regression equations estimated a relationship between production
and time. This relationship was used to estimate production at future
points in time. The equations estimated were of two forms. The first
estimated the values of a and b in the following equation:
production = a(year) + b .
The second regression equation estimated values of c and d in the
following equation:
natural log (production) = c(year) + d.
Both equations are linear equations; the second is identified as
"log"-linear, because the equation is estimated given values that are
the natural logarithms of the production data.
Because of the cyclical nature of acrylic and modacrylic fiber
production, particularly in the years 1973 to 1979, regressions were
run on three distinct time intervals of data. The first case included
annual production data over the entire period 1960 to 1979. The
second and third cases used subsets of the data employed in the first
case. The second case employed annual production data from the years
1970 to 1979 only, and the third case used data from 1975 to 1979
only.
The log-linear regression equation projected growth in domestic
production of acrylic and modacrylic fibers of 8.7 percent using
1960-1979 production data, 3.5 percent using 1970-1979 data, and
9.0 percent using 1975-1979 data. The growth rate projected using
1970-1979 data was determined to have the best statistical fit to the
9-39
-------
data. Also? this time interval'allows for some adjustments by producers
In resppqsfi |g general economicicpnditipns, and captures the effects
of the leye] of maturity of the1 industry and pf market cycles of the
industry.
Linear regression equations, do not project a constant growth rate
as dp logrlipear regression equations,, byt rather estimate a discrete
growth rate assoctatgd with every ppi.nt in time. Again, the time
interval 1970-1§7§ provided a prp.jle
-------
Year
1980
1981
1982
1983
1984
1985
1986
1987
Growth
Rate
%
1.9
1.9
1.9
1.6
1.6
1.6
1.6
1.6
Estimated
Production
(gigagrams)
351.4
358.0
364.8
370.7
376.7
382.6
388.7
395.0
Estimated
Production
Capacity
(qiqagrams)
394.6
394.6
394.6
394.6
396.5
402.7
409.2
415.8
Estimate
Capacity
Shortf al 1
(qigagrams)
0
0
0
0
1.9
8.1
14.6
21.2
Estimated production capacity is the larger of 1) the capacity
estimated to be in place in 1980 and 2) the capacity required, at a
95 percent capacity utilization rate, by estimated production. The
production capacity estimated to be in place in 1980 is 394.6 gigagrams
(see Table 9-7). Estimated capacity shortfall is the difference
between the estimate of current capacity, and the capacity needed to
meet the production estimates at a 95 percent capacity utilization
rate, that is, the column "Estimated Production Capacity".
The second published growth projection, from the January 1981
issue of Textile Organon, was a projection of 2.7 percent growth
through 1985. Again 1979 was used as the base year, with production
of 344.8. (The projection has been extended to 1987 for comparative
purposes.)
Year
1980
1981
1982
1983
1984
1985
1986
1987
Growth
Rate
%
2.7
2.7
2.7
2.7
2.7
2.7
2.7
2.7
Estimated
Production
(qigagrams)
354.1
363.7
373.5
383.6
393.9
404.6
415.5
426.7
Estimated
Production
Capacity
(qigaqrams)
394.6
394.6
394.6
403.8
414.6
425.9
437.4
449.2
Estimated
Capacity
Shortf al 1
(gigagrams)
0
0
0
9.2
20.2
31.3
42.8
54.6
Estimated production capacity and estimated capacity shortfall
were calculated as described above.
As mentioned, in-house linear and log-linear regressions were
estimated to project further estimates of growth in the acrylics and
9-41
-------
modacrylics market. Both projections were based upon annual production
data from 1970-1979. These data are:
Year
1970
1971
1972
1973
1974
1975
1976
1977
1978
1979
Production
(qigagrams)
222.8
247.0
283.5
336.2
285.9
237.6
281.3
321.1
328.7
344.8
Two equations were estimated. The first was a direct linear equation
and was of the form:
prodt =
(t)
where
prod = production estimated in year t
t = year, t = 1970, 1971,...1979
= intercept of fitted line
= slope of fitted line
The coefficients estimated were:*
prod. = -19395.08000000 + 9.96909091(t)
r (7142.500) (3.617)
R2 = 0.487
This equation was then used to make projections of production for the
years 1980-1987.
Year-
Growth Estimated
Rate Production
(qiqagrams)
1980
1981
1982
1983
1984
1985
1986
1987
2.9
2.8
2.7
2.7
2.6
2.5
2.5
2.4
343.7
353.7
363.7
373.6
383.6
393.6
403.5
413.5
Estimated
Production
Capacity
(qiqaqrams)
394.6
394.6
394.6
394.6
403.8
414.3
424.7
Estimated
Capacity
Shortf al 1
(qiqaqrams)
0
0
0
0
9.2
19.7
30.1
435.3
40.7
*The standard error for each estimated value is provided in parentheses
beneath each estimated value.
9-42
-------
Estimated production is obtained by substituting the value of the year
in the regression equation obtained from historical data. For example,
substituting t = 1980 into the direct linear equation for acrylic and
modacrylic fiber yields:
prodt = -19395.08 + 9.96909091 (1980)
prod = 343.7
I*
Estimated production capacity and estimated capacity shortfall were
calculated as described above.
The second equation estimated was log-linear and was of the form:
In(prodt) = + (t)
All definitions from above hold. The coefficients estimated were:*
ln(prod.) = -64.14961461 + 0.03535337(t)
t (25.414) (0.013)
R2 = 0.485
This equation was used to project production levels of:
Year
1980
1981
1982
1983
1984
1985
1986
1987
Growth
Rate
3.5
3.5
3.5
3.5
3.5
3.5
3.5
3.5
Estimated
Production
(gigagrams)
347.3
359.7
372.7
386.1
400.0
414.4
429.3
444.8
Estimated
Production
Capacity
(gigagrams)
394.6
394.6
394.6
406.4
421.1
436.2
451.9
468.2
Estimated
Capacity
Shortf al 1
(gigagrams)
0
0
0
11.8
26.5
41.6
57.3
73.6
Estimated production is obtained by substituting the value of the year
in the regression equation obtaned from historical data. For example,
substituting t = 1980 into the log-linear equation for acrylic and
modacrylic fiber yields:
log (prodt) = -64.14961461 + 0.03535337 (t)
*The standard error for each estimated value is provided in parentheses
beneath each estimated value.
9-43
-------
log (prodt) = 5.85005799
prodt = 347.3
Estimated production capacity, and estimated capacity shortfall
were calculated as described above.
Table 9-20 presents the range of projected capacity shortfalls in
1987. The range was constructed from the highest and the lowest
estimates of the four estimates for capacity shortfall presented
above. Two assumptions are included in these calculations. They are:
(1) Any capacity shortfall before 1982 will be met by debottlenecking
existing capacity or by constructing new capacity prior to 1982
(the first year that the NSPS will be in effect). Thus, only the
capacity shortfall occurring in the years 1982-1987 will support
new capacity in 1982-1987.
(2) Because all the model plants are capable of producing modacrylics,
it is assumed that all new capacity built will have the configuration
of Model Plant 2, as Model Plant 2 is the least costly of the
three plants (see Section 9.2.2.2).
9.1.3 Acetate and Triacetate Fibers
9.1.3.1 Production
9.1.3.1.1 Product description. All cellulosic fibers (acetate,
i
diacetate, triacetate, and rayon) are composed of cellulose acetate,
produced by combining cellulose with acetate from acetic acid and
acetic anhydride. This process is called acetylation. The cellulosics
are differentiated by the percentage of hydroxyl groups that are
acetylated in the cellulose molecule. According to the U.S. Federal
Trade Commission classification, rayon has less than 15 percent acetylation,
cellulose acetate or diacetate has 15 to 92 percent acetylation, and
g
cellulose triacetate has not less than 92 percent acetylation.
9.1.3.1.2 Production technology. Complete acetylation of cellulose
is the first step in the production of both acetate and triacetate.*
Cellulose acetate for textile fiber production is obtained by controlled
partial hydrolysis of cellulose triacetate. The cellulose acetate or
throughout this chapter the term acetate refers to both acetate and
diacetate fibers.
9-44
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9-45
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triacetate polymer is then usually dissolved in a solvent for extrusion.
Fiber is produced by dry spinning, in which the filaments are extruded
into a column of hot inert gas. As the filaments dry, the acetone
solvent evaporates, leaving a fiber of almost pure cellulose acetate
or triacetate. After spinning, treatment of the fiber varies with the
end use anticipated. Acetate yarn is lubricated and wound onto a
bobbin as continuous filament yarn with no further treatment. Cigarette
filtration tow (cellulose acetate) is lubricated, crimped and dried.
9.1.3.1.3 Production history. Cellulose acetate fibers were
first produced commercially in the United States in 1924 by the Celanese
Corporation. The fabric woven from these fibers is characterized by
drapability, softness, and shrink and mildew resistance. The fabrics
are sold both as end products and for manufacture into top-type and
bottom-type apparel, lingerie, linings, draperies, and upholstery.,
The alternate primary use of cellulose acetate fibers is cigarette
filtration tow.
Cellulose triacetate fibers were first produced in the United
States in 1954, also by Celanese Corporation. The fibers contain a
higher ratio of acetate to cellulose than do acetate fibers. Fabrics
woven from these fibers are characterized by shrink and wrinkle resistance
and pleat retention. The fabrics are marketed both as end products
and as inputs to dress, skirt, and sportswear manufacture.
9.1.3.1.4 Role in U.S. economy. The shares of GNP, employment,
and new capital expenditures contributed by the cellulose acetate and
triacetate fibers industry provide measures of the significance of the
industry in the national economy. The most recent industry data
available to calculate these shares are contained in the 1977 Census
of Manufactures. Data from this source are not disaggregated for the
acetate and triacetate industry, but grouped with the rayon industry.
This larger industry is defined as SIC 2823, Cellulosic Manmade Fibers.
The cellulosic fibers industry contributed 0.04 of 1 percent to
total GNP and 0.02 of 1 percent to total employment in 1977. Of the
expenditures on new plant and equipment by all industries that year
the cellulosics fiber industry accounted for 0.02 of 1 percent.
9-46
-------
Like acrylic and modacrylic fibers, cellulosic fibers are intermediate
goods. They consume output of the wood pulp and petrochemical industry
and are used as inputs to the textile and cigarette industries. To
the extent that these fibers are major consumers of particular petro-
chemicals, or have poor substitutes in their alternative end-use
applications, they may be a critical factor in the economic health of
other industries. This is most probable in the cigarette filtration
tow application of the fibers.
9.1.3.1.5 Factors of production. The principal materials used
to produce acetate and triacetate fibers are wood or cotton 1 inters
pulp, acetic acid, acetic anhydride and acetone. The cellulose pulp
used for polymer production must be of high purity and have an alpha
cellulose content of approximately 94 percent. Wood pulp is less
expensive than cotton 1 inters pulp and is currently preferred by
acetate and triacetate fiber producers. Domestic sources of wood pulp
are ITT Rayonier, Inc., International Paper, Buckeye Cellulose, and
Weyerhaeuser Company. Some wood pulp is imported for acetate manufacture,
The solvent currently used by the industry is acetone, but other
solvents such as a chlorinated hydrocarbon are also compatible with
the process.
The major producers of acetate and triacetate, Celanese Corporation
and Eastman Kodak, have captive sources of acetic acid. All producers
have captive sources of acetic anhydride. Eastman Kodak also has a
51
captive source of acetone. The principal feedstocks, wood pulp and
acetone, appear to have a variety of alternative uses. This makes a
more competitive and observable market for inputs than was the case
for acrylic and modacrylic fibers production.
Acetone is of particular interest because it is the volatile
organic chemical (VOC) that the proposed standards aim to control. It
is a petrochemical produced both as a coproduct with phenol and by
dehydrogenation of isopropyl alcohol. The market for phenol determines
the output of acetone as a coproduct. In general, acetone capacity
has been underutilized in recent years and this, in conjunction with
the possible entry of new competitors to acetone as a methyl methacrylate
feedstock, seems to insure ready supplies of acetone in the near to,
52
intermediate future.
9-47
51
-------
Acetate and triacetate fibers producers integrate the acetylation
step with fiber spinning and product finishing. The technology is
well understood and both it and the equipment can be readily purchased.
The other principal purchased inputs to the production of acetate
and triacetate fibers are labor and equipment. The majority of the
five plants currently producing these fibers were built in the 1930s
and 1940s.53 The production of these fibers is said to be mature.
Productivity is being increased by debottlenecking but no major changes
in the technology itself, or in the ratio of process inputs, is foreseen.
Increased solvent recovery, whether due to the proposed standards; or
to economic considerations, may be the most dramatic instance of
factor substitution considered by producers. A fundamental limitation
on factor'substitution is the technically fixed ratio of cellulose
acetate polymer to polymer fibers; the polymer already accounts for
the bulk of production costs.
9.1.3.2 Supply Conditions.
9.1.3.2.1 Domestic producers. The domestic acetate and triacetate
fiber producers and their production capacities are listed in Table -9-21.
Three companies produce fibers at five plant locations: Celanese
Corporation (with three plants), Eastman Kodak, and Avtex Fibers, Inc.
Two acetate plants were closed in the mid-1970s; Du Pont closed a 22.6
gigagram-per-year plant in Waynesboro, Virginia, and Celanese Corporation
closed a 13.6 gigagram-per-year plant in Rome, Georgia. Both plants
produced cellulose acetate yarn.
In 1980, cellulose acetate and triacetate fibers in all forms
ranged from $2.40 to $2.98 per kilogram, or $1.09 to $1.35 per pound
(see Section 9.2.3.4). Given the bulkiness of the output, this is a
relatively low value-to-weight ratio. As would be expected, fiber
producers are located relatively close to their customers in order to
minimize transport costs and thereby enhance their competitiveness.
Like acrylic and modacrylic producers, acetate and triacetate fiber
producers are clustered in the southeastern United States.
Production of acetate and triacetate fibers in the United States
from 1960 to 1980 is shown in Table 9-22. At the beginning of this
period, yarn accounted for 58 percent of output of the acetate fibers
9^48
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industry. Staple and tow accounted for 42 percent of the output, with
approximately 15 percent going to the textile market and 27 percent
going to cigarette filtration tow. From 1960 to 1970 yarn production
grew fairly steadily at an average annually compounded rate of approximately
7 percent. In the early and mid 1970s, yarn production went into a
severe slump; production declined every year until 1978 and 1979.
Yarn production in 1979 was only 38 percent greater than in 1960, and
production again fell in 1980. Production of staple and tow for
textile fibers fell steadily, comprising only 0.1 of 1 percent of
total acetate and triacetate production in 1979. Production of cigarette
filtration tow, on the other hand, increased dramatically over the
period 1960 to 1979 (6.6 percent average annually compounded growth),
constituting nearly 53 percent of total output of cellulose acetate
and triacetate fibers in 1979. Total output has increased at an
average annual rate of 3.0 percent per year.
The role of U.S. acetate and triacetate textile fiber in world
production is substantial. As shown in Table 9-23, the United States
produced over 42 percent of world acetate and triacetate textile fiber
in 1978. While this is a slight decline in the percentage of world
production from the early years of the decade (46 to 50 percent), it
does not appear to represent a direct loss of the U.S. share of the
world market since such a small quantity of this yarn is exported from
the United States and imports of foreign fiber are negligible. Table 9-23
also shows, however, that U.S. capacity was expected to fall below
40 percent of world capacity in 1980. The declining share of the
United States in world production of textile yarn may ultimately
result in more indirect if not direct world competition for domestic
acetate and triacetate fiber producers.
U.S. production of cigarette filtration tow has had a larger and
more stable role in the world market than acetate yarn production. As
shown in Table 9-24, the United States accounted for 51 percent of
world cigarette filtration tow production in 1978. The world/U.S.
interface in this market is particularly critical because so much of
U.S. produced filtration tow is exported, and because cigarette exports
themselves are a substantial and growing market for U.S. producers.
9-51
-------
TABLE 9-23. PRODUCTION AND PRODUCING
CAPACITY OF ACETATE AND TRIACETATE
TEXTILE FIBER59
(gigagrams)
United States
World
Production
1972 182
1973 198
1974 164
1975 137
1976 130
1977 128
1978 137
Producing capacity
1979 148
1980 148
377
399
359
316
309
310
324
359
371
TABLE 9-24. PRODUCTION OF CIGARETTE FILTRATION TOW60
(gigagrams)
Europe
United States ,
Other American
Asiac
Total
1971
38
94
18
23
173
1972
43
102
19
26
190
1973
45
116
22
28
211
1974
48
124
25
30
227
1975
49
130
26
36
241
1976
58
137
27
37
259
1977
67
144
27
39
277
1978
73
150
31
40
294
Belgium, West Germany and United Kingdom
Brazil, Canada, Columbia, Mexico and Venezuela
Japan and South Korea
9-52
-------
9.1.3.2.2 Industry structure and capacity. The production of
cellulose acetate and triacetate is very concentrated; the largest
firm (Celanese Corporation) controls 52.5 percent of the total acetate
and triacetate capacity. Celanese and Eastman Kodak together control
over 93 percent of the total capacity, with the remaining 6.9 percent
belonging to Avtex. Distinguishing between textile yarn and cigarette
tow increases the degree of market concentration: Celanese owns
70 percent of textile acetate and triacetate yarn and staple capacity,
and Eastman Kodak owns 66 percent of cigarette tow capacity. Qualitative
data suggest that the producers of cellulose acetate and triacetate
fiber do not compete directly with one another because each has expanded
into distinct end-use markets; each producer determines the market
practices for the major end-use categories that it dominates. The
degree of industry concentration suggests weak local competition as
wel 1.
Aggregate production capacity for the' textile fiber portion of
the acetate and triacetate industry is shown in Table 9-25. These
capacity figures reflect the trends in production discussed above and
reflect a recent estimate of capacity decline (1979 to 1980). While
these figures are only for textile fiber capacity, they show considerable
annual variation and suggest that marginal adjustments in capacity are
relatively easy. A comparision of these capacity figures with the
corresponding production figures in Table 9-22 shows that in 1979
capacity utilization was approximately 90 percent. Historical data
for this industry indicate, however, that this rate does not imply
capacity expansion.
Cigarette filtration tow capacity data were not available as a
time series. The production series, in conjunction with recent firm
data and contacts with the industry, suggest that this capacity has
been expanding steadily due to debottlenecking and conversion of
equipment from cellulose acetate yarn.
9.1.3.2.3 Industry performance. Table 9-26 provides financial
data for the years 1977 through 1979 for the publically owned producers
of cellulose acetate and triacetate fibers. It is evident that net
sales and earnings before interest and taxes have at least maintained
9-53
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pace with, if not exceeded, the rate of inflation over this period.
Celanese reduced its nominal (and real) amount of long-term debt over
these years; Eastman Kodak increased its nominal debt, but its real
level of debt apparently fell. Both companies appear to be financially
sound. However, aggregate firm data such as these indicate little
about the profitability of the fiber divisions within these companies.
Net sales data for these companies and for Avtex Fibers are presented
in Table 9-27. It appears that only Celanese has increased its fiber
sales in real terms. Fiber sales by both Eastman Kodak and Avtex over
this period are negative when netted of inflation. Given the escalating
prices evidenced for polymer and solvent, it would appear that at,
least Eastman Kodak and Avtex Fibers (and possibly Celanese) have been
experiencing declining rates of return in their fibers divisions.
Avtex1 position over this period appears to be especially difficult
because 100 percent of its sales are due to fiber production.
These data on aggregate fiber sales indicate little about the
profitability of cellulose acetate and triacetate fiber production.
However, the data do suggest that manmade fiber manufacturing in
general has not been earning rates of return that would suggest capacity
additions without cost reductions or price increases.
9.1.3.3 Demand Conditions. The demand for acetate and triacetate
fibers, like that for acrylic and modacrylic fibers, is driven by a
wide variety of end uses. Consequently, the complex set of complementarity
and substitutability relationships at both final and intermediate
points of production affect demand. This is perhaps particularly true
of acetate and triacetate fibers because of the role of the cigarette
industry as a principal consumer of these fibers.
9.1.3.3.1 Fiber end uses. Table 9-28 presents time-series data
of general end-use categories for the shipments of acetate and triacetate
textile yarn. From 1964 to 1975, apparel end use was the dominant
general category (86 percent of shipments to domestic consumers in
1975). Use in home-furnishings was modest (12.7 percent); industrial
and other end uses accounted for the residual (1.3 percent).
A more detailed array of end uses for 1968-1975 is presented in
Tables 9-29 and 9-30. Within the apparel end uses, underwear and
9-56
-------
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9-59
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nightwear, and bras and foundations, have been rapidly declining
sources of demand. Shipments of top-type fabrics and bottom-type
fabrics also decreased over this period.
Cigarette filtration tow production for 1960-79 is presented in
Table 9-31. Over the period from I960 to 1975, shipments to U.S.
manufacturers grew at an average annually compounded rate of approximately
5 percent. The most interesting aspect of filtration tow end use is
the rapidly growing role of exports both absolutely and relative to
U.S. production.
9.1.3.3.2 Foreign trade. Data for export shipments of acetate
and triacetate textile yarn are contained in Table 9-32. Export
shipments have far exceeded domestic industrial end use, yet accounted
for just over 10 percent of total production in 1980.
As mentioned, exports of cigarette filtration tow have grown
rapidly, averaging 14 percent compounded annually over the period
1960-1975.
9.1.3.4 Projections. Projections of growth for cellulose acetate
and triacetate fibers were found in two publications, the Chemical
Economics Handbook and Textile Industries. The Chemical Economics
Handbook (SRI International) contains growth projections published in
November 1976. Consumption of all cellulose acetate fibers, both for
textile use and for cigarette filtration tow, were projected to decline
73
an average of 0.3 percent per year over the period 1975-1981.
SRI also provided distinct projections for the two types of
acetate fibers. Consumption of cellulose acetate and triacetate
textile fibers was projected to decline at an average annual rate of
74
3.5 percent over the period 1975 to 1981. Imports and exports of
these fibers do not constitute significant markets; exports of acetate
yarn accounted for just over 10 percent of total production of acetate
yarn in 1980 (see Table 9-32). Data for imports of acetate yarn are
not available disaggregated from data for imports of acetate and rayon
yarn; however in 1978 imports of these two fibers together were only
no
12.5 gigagrams. The projected growth rate for domestic consumption
is therefore applicable without much error to growth in production.
9-60
-------
TABLE 9-31. EXPORTS OF CELLULOSE ACETATE FILTRATION TOW 58 67 68 69
(gigagrams)
Production3
Year United States
1960
1961
1962
1963
1964
1965
1966
1967
1968
1969
1970
1971
1972
1973
1974
1975
1976
1977
1978
1979
49
53
58
60
70
71
69
72
73
77
84
94
102
116
124
130.
137d
144d
150^
166e
World
56
64
74
82
100
109
118
123
128
136
154
173
190
211
227
259d
232d
277d
294°
314e
U.S. exports
7
9
12
12
22
22
19
20
24
27
22
20
25
32_
39C
.47C
Exports as
percent of total
U.S. production
14
17
21
20
31
31
28
28
33
35
26
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25
28
31
36
Reference 67
Reference 68
°Reference 58
j
Reference 69
Reference 4
9-61
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9-62
-------
SRI forecast growth in production of acetate fiber for cigarette
filtration tow at an average annual rate of 4.8 percent over the
period 1975 to 1981. This growth rate was the result of projected
growth in export markets of 5.7 percent and growth in domestic consumption
75
of 4.3 percent over the period. However, as mentioned, this projected
growth in domestic consumption does not offset the projected decline
in domestic consumption of acetate textile fiber, giving a net effect
of 0.3 percent dec!ine in consumption for all cellulose acetate fibers.
Textile Industries in its February 1979 issue projected that
domestic mill consumption of rayon and acetate textile fibers together
49
would decline 2.0 percent per year over the period 1977 to 1987.
This projection is not as straightforward as the SRI projections in
that acetate textile fiber growth is not projected independently of
the growth or decline in the market for rayon. In 1979, rayon comprised
65 percent of production of rayon and acetate textile fibers; therefore
market conditions particular to rayon may be dominating those of the
acetate textile fiber market in this aggregate projection.
Shortcomings exist in these projections from published sources.
The projections from the Chemical Economics Handbook are for the
period 1975-1981. The projections were derived from data no more
recent than 1975. These projections are not applicable for forecasting
growth through 1987, given general economic conditions from 1976-1980
and the specific effects that the higher prices of petroleum-derived
products evidenced during 1976-1980 have on the costs of producing
solvent-spun cellulose acetate fibers. The projections from Textile
Industries are less than satisfactory due to the aggregation of the
rayon and acetate markets.
Because of these shortcomings, the EPA estimated regression
equations using historical production data for each of the two types
of cellulose acetate fiber, textile fiber and cigarette filtration
tow. The regression equations conducted in-house estimated projected
growth in the production of these two fibers.
The regression equations estimated a relationship between production
and time. This relationship was used to estimate production at future
9-63
-------
points in time. The equations estimated were of two forms. The first
estimated the values of a and b in the following equation:
production = a(year) + b .
The second regression equation estimated values of c and d in the
following equation:
natural log (production) = c(year) + d.
Both equations are linear equations; the second is identified as
"log"-linear, because the equation is estimated given values that are
the natural logarithms of the production data.
For each type of fiber both log-linear and linear equations were
estimated. As was the case with acrylic and modacrylic fibers, the
two specifications were each estimated for three time intervals of
annual production data: 1960-1979, 1970-1979, and 1975-1979. :
For cellulose acetate textile fibers, the regressions estimated
for data for 1975-1979 were judged to be the best for'the purpose of
forecasting future production. The log-linear growth equation projected
growth in production to be 1.0 percent at an annually compounded rate.
The growth rates estimated by linear regression were a range from
1.0 percent growth in 1981 declining to 0.9 percent growth in 1987.
Log-linear regressions on production data for 1960-1979 and for 1970-1979
both estimated negative growth rates for acetate textile fiber consumption.
Both evidenced a 0.6 percent average annual decline in production.
The growth rates estimated by regression of 1975-1979 production
data were selected as the best indicators of future growth in production
of cellulose acetate textile fibers. This time interval was chosen
because of a stabilization in the demand for these textile fibers,
which occurred in the late 1970s (see Table 9-32).
For cigarette filtration tow, the best statistical fit was provided
by the regression equations run on the 1970-1979 production data. The
log-linear regression equation projected growth in production of
cellulose acetate filtration tow at an average annual rate of 7.2 percent.
The linear regression model projected average annual growth of 4.7
percent in 1981, declining to 3.6 percent in 1987.
9-64
-------
As was the case with the regression equations estimated for
acrylic and modacrylic fibers, the equations do not explicitly take
into account the distinct effects of underlying market forces. Such
influences as national economic trends, interfiber competition
(substitutability, relative prices), and growth or decline in import
and export markets are captured to some extent in the annual production
data. However, there is some error in using this data as a basis for
projection in that first, the effects are not estimated separately and
second, the historical effects will not necessarily pertain in the
future.
Specifically in the case of production of solvent-spun fibers
from petroleum-derived polymer, the future effects of continually
escalating polymer and solvent costs may not be as they were historically.
It is not clear to what extent the growth rates derived by regression
of historical production data are accurate in light of these shortcomings.
Of the published and derived growth rates for cellulose acetate
fibers, those from published sources were not considered accurate for
projection of capacity shortfalls in 1987. The Chemical Economics
Handbook projections were based on data no more recent than 1975, and
were only applicable for growth through 1981. The Textile Industries
projection was for rayon and cellulose acetate textile fibers together;
the applicability of the projection to consumption of cellulose acetate
textile fiber alone is uncertain. Therefore, only the growth projections
estimated by in-house regression were used to project capacity shortfalls.
As mentioned, for cellulose acetate yarn, regressions estimated
using annual production data from 1975-1979 were chosen due to a
stabilization in the demand for these textile fibers that occurred in
the late 1970s. These annual production data are:
Year
1975
1976
1977
1978
1979
Production
(qigagrams)
136.5
130.0
127.7
136.3
143.6
9-65
-------
The first regression, in direct linear form, estimated the equation to
be:*
prod+ = -2628.94000005 + 1.40000000 (t)
* (3975.230) (2.01)
R2 = 0.139
The estimated production levels and growth rates were:
Year
1980
1981
1982
1983
1984
1985
1986
1987
Growth
Rate
%
1.0
1.0
1.0
1.0
0.9
0.9
0.9
0.9
Estimated
Production
(gigagrams)
143.1
144.5
145 j 9
147.3
148.7
150.1
151.5
152.9
Estimated
Production
Capacity
(gigagrams)
150.6
152.1
153.6
155. 1
156.5
158.0
159.5
160.9
Estimated
Capacity
Shortf al 1
(gigagrams)
2.6
4.1
5.6
7.1
"8.5
10.0
11.5
12.9
Estimated production is obtained by substituting the value of the
year in the regression equation obtained. Estimated production capacity
is the larger of 1) the capacity estimated to be in place in 1980, and
2) the capacity required, at a 95 percent capacity utilization rate,
by estimated production. The capacity of cellulose acetate yarn
estimated to be in place in 1980 is 148.0 gigagrams (see Table 9-23).
Estimated -capacity shortfall is tip difference between the estimate of
current capacity, and the capacity needed to meet the production
estimates at a 95 percent capacity utilization rate, that is, the
column "Estimated Production Capacity."
The second equation estimated was log-linear and resulted in the
following equation:* .
ln(prod.) = -14.58050188 + 0.00987012(t)
r (28.744) (0.015)
R2 = 0.133
*The standard error for each estimated value is provided in parentheses
beneath each estimated value.
9-66
-------
The equation was used to project production levels of:
Year
1980
1981
1982
1983
1984
1985
1986
1987
Growth
Rate
%
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
Estimated
Production
(gigagrams)
142.9
144.3
145.8
147.2
148.7
150.2
151.6
153.2
Estimated
Production
Capacity
(gigagrams)
150.4
151.9
153.5
154.9
156.5
158.1
159.6
161.3
Estimated
Capacity
Shortf al 1
(gigagrams)
2.4
3.9
5.5
6.9
8.5
10.1
11.6
13.3
Estimated production, estimated production capacity, and estimated
capacity shortfall were calculated as described above.
To project capacity shortfalls in the cigarette filtration tow market,
regressions were estimated using annual production data from 1970-1979.
These data are:
Year
Production
(gigagrams)
83.8
93.8
101.9
116.0
123.7
130.0
136.8
143.6
149.9
165.3
The direct linear estimation was:*
prod. = -16251.09555556 + 8.29333333(t)
t (749.821) (0.380)
R2 = 0.986
*The standard error for each estimated value is provided in parentheses
beneath each estimated value.
9-67
-------
The equation was used to project production levels of:
Year
1980
1981
1982
1983
1984
1985
1986
1987
Growth
Rate
%
4.9
4.7
4.5
4.3
4.1
3.9
3.8
3.6
Estimated
Production
(qiqaqrams)
169.7
178.0
186.3
194.6
202.9
211.2
219.5
227:8
Estimated
Production
Capacity
(qigagrams)
178.6
187.4
196.1
204.8
213.6
222.3
231.1
239.8
Estimated
Capacity
Shortf al 1
(qiqagrams)
4.6
13.4
22.1
30.8
39.6
48.6
57.1
65.8
Estimated .production is obtained by substituting the value of the year
in the regression equation obtained. Estimated production capacity is the
larger of 1) the capacity estimated to be in place in 1980 and 2) the
capacity required, at a 95 percent capacity utilization rate, by estimated
production. The capacity of cigarette filtration tow estimated to be in
place in 1980 was 174.0 gigagramss based upon 1979 production of 165.3
gigagrams (see Table 9-22) and a 95 percent utilization factor.* Estimated
capacity shortfall is the difference between the estimate of current
capacity, and the capacity needed to meet the production estimates at a
95 percent capacity utilization rate, that is, the column "Estimated
Production Capacity."
The second equation, estimated by log-linear regression, was:**
ln(prodj = -136.92203615 + 0.07177904(t)
t (10.443) (0.005)
R2 = 0.963
*Note that this capacity of 174.0 Gg, together with estimated capacity of
148.0 Gg for cellulose acetate yarn, is a total capacity for cellulose
acetate and triacetate fiber of 322 Gg. This contradicts the data of
Table 9-21 (total capacity = 296 Gg). The reported production data, the
reported capacity data, and/or the capacity utilization assumption have
associated errors.
**The standard error for each estimated value is provided in parentheses
beneath each estimated value.
9^-68
-------
The equation was used to project production levels of:
Year
1980
1981
1982
1983
1984
1985
1986
1987
Growth
Rate
%
7.2
7.2
7.2
7.2
7.2
7.2
7.2
7.2
Estimated
Production
(gigagrams)
181.4
194.9
209.4
224.9
241.7
259.7
279.0
299.7
Estimated
Production
Capacity
(gigagrams)
.190.9
205.2
220.4
236.7
254.4
273.4
293.7
315.5
Estimated
Capacity
Shortfall
(gigagrams)
16.9
31.2
46.4
62.7
80.4
99.4
119.7
141.5
Estimated production, estimated production capacity, and estimated
capacity shortfall were calculated as described above for the linear
estimation.
The projected capacity shortfalls, a range for each of the two
cellulose acetate fiber types, are presented in Table 9-33. The
1982-1987 capacity shortfalls are based on the assumption that any
capacity shortfall occurring before 1982 will be met by debottlenecking
existing capacity or by constructing new capacity prior to 1982 (the
first year that the NSPS will be in effect). Thus, only the capacity
shortfalls arising in the years 1982-1987 will support new capacity in
1982-1987.
9.2 ECONOMIC IMPACT ANALYSIS
9.2.1 General Methodology
The purpose of this analysis is to estimate the economic impacts
of the regulatory alternatives presented in Chapter 6. These alternatives
will affect only new fiber producers who use volatile organic compounds
as solvents. Most organic solvent-spun fibers are either acrylic/modacrylic
or cellulose acetate/cellulose triacetate. The other specialty fibers
produced with VOC solvent make up only 2.9 percent of solvent-spun
fiber capacity. Consequently, the economic impact analysis focuses
on possible capacity expansion for acrylics and acetates and the
impact of the regulatory alternatives on the cost, output and price of
these fibers.
The impact analysis for each fiber type begins with a discounted cash
flow analysis based upon the capital and operating costs developed by the
EPA for each of the modelplants. This analysis provides estimates of the
9-69
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relative cost of each of the model plants and the cost impacts of the
various emission control alternatives for each model plant. These
values are therefore the basis for estimates of the cost impact and
assessment of the financing burdens placed on the firms of the industry
by the proposed emission controls.
The discounted cash flow analysis also provides an implicit price
estimate for the output of each of the model plants under the alternate
levels of emission control. These price estimates, in conjunction
with the industry profiles, provide a basis for estimating the market
impacts of the proposed regulations. The market impacts of interest
include effects on price, sales, production and capacity.
9.2.2 New Acrylic and Modacrylic Facilities
For each of three types of model acrylic fiber plants, cost
estimates were made for three alternate levels of VOC emissions control.
Regulatory Alternative I, or the "baseline" level of control, utilizes
a design based on current industry practice for new facilities.
Regulatory Alternatives II and III represent VOC emissions control
beyond the baseline level. Regulatory Alternative II represents
application of additional controls to the primary remaining source of
emissions from a new plant. Similarly, Regulatory Alternative III
represents the application of additional controls to the second most
significant remaining source of VOC emissions. As mentioned in the
industry profile, expansion of acrylics capacity by American Cyanamid
or Badische Corporation (together nearly one-fourth of 1980 industry
capacity) will not be affected by these proposed regulatory controls
so long as neither company utilizes volatile organic solvents.
9.2.2.1 Model Plant Cost Estimates. The fixed capital costs
estimated by the EPA for the various degrees of VOC emissions control
for the three model plants are summarized in Table 9-34. These figures
show that under the control technologies considered by EPA, increases
in VOC emissions control are associated with increases in the fixed
investment made in the plants. These increases were nontrivial;
Regulatory Alternative Ill's fixed capital costs were between 6 and
9 percent greater than the baseline. In addition to fixed capital
costs, Table 9-34 shows working capital costs. Working capital, the
9-71
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average cash on hand required by the firm in order to finance purchases
of labor, materials and product inventory, was estimated to be one-twelfth
of the annual operating costs. The cost of maintaining this average
cash balance was estimated to be the present value of the finance
charges.
In order to assess the significance of these costs for the acrylic
market in general, and new plant choice in particular, the fixed and
working capital cost data were combined with associated operating
costs. These additional expenses are summarized in Table 9-34. They
are based upon 95-percent plant capacity utilization and physical
input requirements derived in Chapter 6.
Solvent costs for DMAc and DMF were estimated using mid-1980 bulk
prices from the Chemical Marketing Reporter: $1.51 per kilogram for
78
DMAc, and $1.09 per kilogram for DMF. Acetone was estimated to cost
$0.62 per kilogram in mid-1980, based on conversations with producers
78 80
of this chemical. ' Because of increased solvent recovery associated
with greater VOC emissions control, the make-up solvent required by
each of the plants declines significantly between the baseline and
Regulatory Alternative III. The associated solvent costs drop by $1.8
million for Plant 1, $1.3 million for Plant 2 and $1.2 million for
Plant 3.
The regulatory alternatives promote improved solvent recovery at
new, modified, and recontructed synthetic fibers plants, and this will
reduce the makeup solvent requirements of these plants. These reductions
are the basis for the computation of a solvent recovery credit: the
amount of solvent saved times the market price of the solvent. These
credits are employed in the economic analysis as an offset to the
capital equipment and operating costs of improved solvent recovery.
Several producers have disputed the use of the market price as a
means of valuing a unit of solvent saved. Specifically, firms which
produced the solvent used in their synthetic fiber production activities
claimed the market price was inflated relative to the internal accounting
value used in firm investment and operating decisions. They therefore
contended that the use of the market price overstated solvent recovery
credits and understated the economic impact of the proposed standards.
9-73
-------
The market price is nontheless considered to be the appropriate
price for computing the solvent recovery credit. This is based upon
the principle, generally accepted in economics, that in a competitive
setting market prices represent the social opportunity cost of resources.
Internal price of accounting cost valuation often reflect sunk cost or
market structure phenomena which, while real enough to the firm, do
not best reflect the value of a good to the economy as a whole. It is
this later perspective which should be the basis for the economic
analysis of a standard.
Furthermore, since the standard would be applied to new sources,
it is not clear that internal accounting costs used in association
with old plants would even be viewed by the firms as the appropriate
measure of the worth of solvent. This is especially true for a vertically
integrated firm, which would require new solvent capacity if it is to
continue to supply its synthetic fiber facilities with solvent. The
opportunity cost of solvent to such a firm is the market price of the
solvent from another source.
Polymer costs were difficult to estimate because no well-developed
market for polyacrylonitrile exists. Acrylic manufacturers actually
purchase the monomer acrylonitrile and polymerize it in-house to
produce polyacrylonitrile. The decision to examine the spinning and
finishing phases of production in Isolation from polymerization in
this analysis has the effect of requiring the estimation of internal
or accounting price for a major process input. The price of polyacrylo-
nitrile was estimated by taking the mid-1980 price of acrylonitrile
from the Chemical Marketing Reporter and adding a processing value of
$0.33 per kilogram.* This procedure yielded a polyacrylonitrile price
estimate of $1.16 per kilogram. For Plant 3, the modacrylic plant,
the polymer price was adjusted to reflect the 40-percent vinylidene
chloride/60-percent acrylonitrile mix that is standard for modacrylic
polymer. The mid-1980 price of vinylidene chloride was estimated at
$0.62 per kilogram. Again, a processing value of $0.33* per kilogram
*Derived from data in the Chemical Economics Handbook Marketing Research
Report on Acrylic and Modacrylic Fibers.
9-74
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was added to incorporate value added in polymerization. Modacrylic
polymer price for Plant 3 was therefore estimated to be $1.07 per
kilogram. The quantity of polymer required as input does not vary by
level of emissions control; therefore the polymer costs for each model
plant do not vary by regulatory alternative.
The category "Other Operating Expenses" shown in Table 9-34
includes labor, administration, utilities, and insurance costs. These
expenses rose slightly as a result of increased VOC emissions control.
Operating expenses plus working capital make up around 95 percent
of the annual expenses incurred by the firms operating these model
plants. The cost of additional emission control equipment, while a
significant fraction of fixed costs, is not a major portion of the
overall expenditures anticipated by a firm considering building and
operating a new acrylic facility.
9.2.2.2 Present Discounted Cash Flow Analysis. The capital and
operating costs for each model plant and each option were employed as
inputs in a cash-flow model to estimate the net present cost and
implicit producer price for each plant for each alternative. The
objective of this analysis is to determine (1) which of the model
plants would be least costly, and (2) what impacts on costs (and
prices) the various levels of VOC emission control would have. The
results of this analysis are summarized in Table 9-35.
The present discounted costs are shown for each plant both before
and after normalization by plant capacity. 'The discount rate employed
to make these discounted cash flow calculations was the estimated
weighted average cost of capital (WACC) for firms producing acrylic,
modacrylic, and cellulose acetate fibers. The WACC was adjusted by an
estimate of long-run inflationary expectation so as to yield a real
discount rate of 4.74 percent for use in the analysis. The details of
these calculations and adjustments are contained in Appendix E.
The 4.74 percent estimate of the industry's real weighted average
cost of capital was the highest of the range of WACCs estimated. The
EPA chose this estimate for the discounted cost and implicit price
calculations because an industry's required rate of return (for which
the WACC is a proxy) is a component of costs, and hence the higher the
9-75
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TABLE 9-35. DISCOUNTED PLANT COSTS AND IMPLICIT PRICE FOR
MODEL ACRYLIC AND MODACRYLIC FIBER PLANTS9
Model
plant
Plant 1
(capacity of
45.36 Gg/yr)
Plant 2
(capacity of
45.36 Gg/yr)
Plant 3
(capacity of
20 Gg/yr)
Level of
control
Baseline
Regulatory
Alternative
Regulatory
Alternative
Baseline
Regul atory
Alternative
Regulatory
Alternative
Baseline
Regulatory
Alternative
Regulatory
Alternative
Discounted
cost of
plant
(million
1980 dollars)
1,778.6
II 1,777.6
III 1,772.3
1,670.3
II 1,671.7
III 1,669.4
771.9
II 768.4
III 765.2
Normalized
discounted
cost of plant
(million dollars
per gigagram
capacity)
39.2
39.2
39.1
36.8
36.9
36.8
38.6
38.4
38.3
Implicit price
of fiber
(dollars
per kilogram)
2.61
2.60
2.60
2.45
2.45
2.45
2.57
2.56
' 2.55
Present discounted values were computed using the following economic parameters:
thirty year plant life, 4.74 percent real rate of discount, fourty-nine percent
effective tax rate, ninety-five percent plant utilization, and ten percent
investment tax credit.
9-76
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WACC, the higher the product price must be to recover all costs. The
EPA has chosen that estimate of the range of WACC estimates that
portrays the "worst case" scenario, in the sense that the higher the
WACC, the greater would be the economic burden associated with investing
in additional capacity.
Model Plant 2 is the most attractive alternative among the two
acrylic fiber plant types: its present discounted costs are approxi-
mately 6 percent lower than those for Model Plant 1. The modacrylic
plant, Model Plant 3, costs less than the other two model plants
because of its smaller capacity. When normalized to an equal capacity,
the cost of the modacrylic facility is slightly less than the cost of
Model Plant 1, but greater than that of Model Plant 2.
The striking thing about the discounted plant costs is that costs
for two of the three model plants decline as emissions control increases.
.For the third model plant (Model Plant 2), Regulatory Alternative III
is no more costly than baseline control, and Regulatory Alternative II
is only slightly more costly. Even in present-value terms, in which a
dollar of initial investment is weighted more heavily than a dollar of
future operating costs, the model plants, for the most part, become
more attractive investments as the level of emissions control increases.
The driving force behind this result is the annual saving in the cost
of solvents. With greater emissions control, the value of the additional
solvent that is captured and recycled more than offsets the increased
cost of the additional control equipment and maintenance.
9.2.2.3 Profit and Price Impact of Emissions Control. Given the
results of the discounted cash-flow analysis, the profit and price
impacts of emissions control are easy to bracket. At the extremes,
the change in costs associated with increased emission control may be
absorbed entirely by consumers, in the form of price changes, or by
producers, in the form of changes in the cost of doing business. In
the case of acrylic and modacrylic fibers, increased emissions control
confers benefits to the party or parties impacted by the change, with
only one exception, moving from baseline control to regulatory
Alternative II control for Model Plant 2. The outcome for the full-price
increase and full-cost absorption cases are shown below.
9-77
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Full-cost pass through
(percent)
Level of control
Baseline to Regulatory
Alternative II
Baseline to Regulatory
Alternative III
Price change
Plant 1 Plant 2 Plant 3
-0.4
-0.4
0.0
0.0
-0.4
-0.8
Level of control
Baseline to Regulatory
Alternative II
Baseline to Regulatory
Alternative III
Full-cost absorption
(million 1980 dollars)
Present value of cost change
Plant 1 Plant 2 Plant 3
-1.0
-6.3
+1.4
-0.9
-6.7
Increased emissions control increases the cost of new facilities in
only one case, and in no case increases the price of output.
These results do, however, deserve some qualification. The
declines in the present discounted cost of the plants as emission
control increases are very small, all less than 1 percent of total
discounted costs. Declines of this magnitude may well be the result
of minor errors in cost estimation. The apparent consistency in the
cost trends across plants may actually'reflect nothing more than a
consistent error in the raw data or cost estimation procedure.
Furthermore, since these control technologies involve the installation
of relatively straightforward enclosure systems, these cost trends
suggest that acrylic producers might well retrofit their current
spinning lines. Although the Du Pont plant was built with such enclosures,
the other acrylic producers have not retrofitted their facilities.
While recognizing these considerations, the EPA believes that for the
range of control and technology choices examined here, the economic
9-78
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impact on the cost or price of acrylics from new production capacity
is relatively small and is quite likely to be negative.
9.2.2.4 Capacity Projections Reconsidered. Ordinarily, one
would expect that the supply of synthetic fiber would be a fairly
smooth function of the price of output and the price of inputs. The
synthetic fiber industry has recently emerged from a period of soft
demand relative to capacity. Theoretically, in such circumstances
firms will remain in production so long as they are able to cover
their variable costs. Firms operating plants whose revenues from
production do not cover the variable costs of that production will
close those plants. As noted in the industry profile, Union Carbide
left the acrylic and modacrylic industry in 1975, by closing its
modacrylics plant. Industry earnings are only now beginning to recover
from the soft demand experienced during the 1974-1975 recession.
In such circumstances, it is quite likely that additions to
capacity must be preceded by a significant increase in the price of
fiber relative to operating costs. Established plants may continue to
produce at the lower prices because the capital costs are sunk.
However, new capacity can only be justified when the price is high
enough to make the expectation of future earnings and profits competitive
with other investments. This set of circumstances may result in a
discontinuous supply function for acrylic and modacrylic fibers, as
pictured in Figure 9-1. In that figure the current capacity of the
industry is Q|. The supply function SQ SQ is discontinuous at Q^:
increases in industry supply beyond Q| will require a price P2 PQ- .
With the supply function, SQ SQ, the dynamics of industry capacity
expansion may be characterized as follows. For a demand function DQ
DO, the industry is operating well below capacity, price is PQ, and
output and consumption of fiber are equal at QQ. Over time, however,
the demand for the fiber increases (shifts to the right) to D-j^ Dp but
capacity and production remain at Q| once that capacity is reached.
The price of fiber, however, rises to P^ Further increases in demand
result only in price changes until price P2 is attained. At that
price new capacity is financially justified and shifts in demand to D2
D2 result in output increases (to Q2) with little or no further effect
9-79
-------
Price
P1
po
Q0 Q1 Q2
Quantity Produced
Figure 9-1. Market With a Supply Discontinuity
9-80
-------
on the price P2< While this is a highly stylized portrayal of a
dynamic market situation, it underscores the possibility that new
acrylic and modacrylic capacity will not automatically be constructed
as current-capacity is approached. A price barrier may first have to
be overcome. This characterization of supply and demand is intended
to reflect the conditions of the current acrylic and modacrylic market.
In the following paragraphs, the current market situation and the
position of the current market equilibrium (En) are considered.
As noted above, the evidence of an earnings slump and firm withdrawal
support the notion of a discontinuity in supply. Another indication
of the existence of a supply discontinuity, as well as of the particular
position of the market equilibrium, might be obtained through a comparison
of the current market price and implicit price for the fiber, which
emerged from the discounted cash flow analysis. Ranges for these
values are presented below.
Prices
(dollar per kilogram)
Market
Implicit
Acrylic
Model Plant 1
Model Plant 2
Modacrylic
Model Plant 3
1.94-2.4982'83'84 2-60-2'61
1.94-2.4982'83'84 2.45
2.38-2.58
85*
2.55-2.57
Because Model Plants 1 and 2 are also capable of producing modacrylic,
it is anticipated that a firm constructing new acrylic or modacrylic
facilities would build a plant like Model Plant 2, which is the least
cost plant. The implicit price estimated for Model Plant 2 falls just
within the high end of the range for acrylic prices reported for
mid-1980.
*These prices are for January 1981, not mid-1980. Mid-1980 prices were
not available from the source.
9-81
-------
The market prices presented here are a very broad range, reflecting
differences in the prices of various types of acrylics, for example,
thick fibers for use in manufacturing carpets and thin fibers for use
in apparel.
Additionally, market prices for acrylic and modacrylic fibers
have recently been quite volatile. By March 1981, acrylic fiber
OO Qfl
prices were reported ranging from $2.31 to $2.69, ' and modacrylic
ojr
prices were reported ranging from $2.60 to $2.80. Given the recent
increases in prices for inputs to acrylic and modacrylic production
(see Table 9-36), it is quite likely that modacrylic and acrylic price
increases were lagging behind input price increases. If indeed a
supply discontinuity existed in the market for acrylic and modacrylic
fibers between the market prices for these fibers in mid-1980 and the .
implicit prices necessary to justify new capacity construction, this
price differential appears to have been traversed. It seems quite
reasonable that producers of acrylic and modacrylic prices would no
longer be deterred from capacity addition, in that current market
prices of acrylic and modacrylic fibers justify the construction of
new plants. Therefore, the cost associated with constructing plants
to meet either baseline levels of control or NSPS levels of control do
not seem to be prohibitive to construction of new plants to meet the
capacity shortfall projected for the acrylics and modacrylics fiber
industry (see Section 9.1.2.4 above).
9.2.3 New Acetate and Triacetate Facilities
The fixed capital costs estimated for two types of new acetate
fiber capacity were presented in Chapter 8. The model plants considered
both employ acetone solvent and dry spinning but produce different
finished products due to processing differences. Plant 4 produces .
cigarette filtration tow and Plant 5 produces textile fibers. As in
the case of acrylics and modacrylics three degrees of VOC emission
control are analyzed: Regulatory Alternative I, the baseline or
current industry practice for new plants; Regulatory Alternative II,
application of additional controls to the major remaining source of
VOC emissions; and Regulatory Alternative III, additional control of
both the first and second most significant remaining sources.
9-82
-------
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9-83
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y
9.2.3.1 Model Plant Cost Estimates. The fixed capital costs as
estimated by the EPA for various degrees of control are summarized in
Table 9-37. These data show that fixed equipment costs increase with
the level of VOC emissions control. The size of this increase varies
substantially between the plants. Between the baseline level of
control and Regulatory Alternative III, fixed capital costs rise
6.3 percent for Plant 4 and 12.4 percent for Plant 5. As in the case
of acrylic and modacrylic model plants, the working capital costs were
estimated to be the present value of maintaining an average cash
balance equal to one-twelfth of annual operating costs. ;
Estimated annual operating expenses for the cellulose acetate
model plants are also summarized in Table 9-37. These operating costs
v/ere developed in a fashion similar to that described above for acrylics.
The costs were estimated for the physical input requirements
presented in Chapter 6, assuming 95-percent capacity utilization.
Cost of solvent was assumed to be $0.62 per kilogram and was based on
EPA communications with producers of this solvent. ' Because of
the increased recovery of solvents for additional levels of VOC control,
the cost of solvent for Plant 4 dropped $0.7 million per year of
operation between the baseline and Regulatory Alternative II, and $1.0
million per year of operation between the baseline and Regulatory
Alternative III. Similarly, the cost of solvent for Plant 5 dropped
$0.9 million and $1.3 million per year between the baseline and Regulatory
Alternatives II and III, respectively.
The cost of cellulose acetate polymer was estimated to be $1.95
per kilogram, as reported in the July 28, 1980, issue of the Chemical
Marketing Reporter. The cost of pblymer per year of operation does
not vary by level of emissions control because the quantity of polymer
required as a process input is constant.
Other operating expenses rose, slightly as the level of VOC emissions
control increased. These increases were 3.5 percent for Model Plant 4
and 6.3 percent for Model Plant 5 as emissions control increased from
the baseline to Regulatory Alternative III.
9.2.3.2 Present Discounted Cash Flow Analysis. The effect of
these opposing expenditure movements on the discounted cost of the
9-84
-------
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9-85
-------
plants is shown in Table 9-38. The results for Model Plants 4 and 5
are different from those for the acrylic and modacrylic plants,, where
discounted costs were found to decline as emission control increased.
In the case of the cellulose acetate plants, discounted costs and
associated implicit prices either are stable or increase as the level
of emission control increases. Solvent recovery credits are not
sufficiently large in some cases to completely offset increases in
capital and operating costs due to increasing levels of emission
control.
9.2.3.3 Profit and Price Impact of Emissions Control. A<; is the
case for acrylics and modacrylicss the estimated price and cost impacts
of the proposed levels of VOC emissions control for cellulose acetate
fibers were based upon the results of the discounted cash flow analysis.
This was done for each of the extreme cases: full-price pass through
to consumers and full-cost absorption of the price impact by producers.
These calculations are presented below.
Full-cost pass through
(percent)
Price change
Level of control
Baseline to Regulatory
Alternative II
Baseline to Regulatory
Alternative III
Level of control
Baseline to Regulatory
Alternative II
Baseline to Regulatory
Alternative III
Plant 4
+0.3
+0.3
Plant 5
+1.7
+1.7
Full-cost absorption
(million 1980 dollars)
Present value of cost change
Plant 4 Plant 5
+3.0
+2.6
+16.2
+16.8
9-86
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TABLE 9-38.
DISCOUNTED PLANT COSTS AND IMPLICIT PRICE FOR
MODEL CELLULOSE ACETATE FIBER PLANTS3
Model
plant
Plant 4
(capacity of
22.7 Gg/yr)
Plant 5
(capacity of
22.7 Gg/yr)
Level of
control
Baseline
Regulatory
Alternative
Regulatory
Alternative
Baseline
Regulatory
Alternative
Regulatory
Alternative
Discounted
cost of
plant
(million
1980. do liars)
1184.4
II 1187.4
III 1187.0
1233.0
II 1249.2
III 1249.8
Normalized
discounted
cost of plant
(million dollars
per gigagram
capacity)
52.2
52.3
52.3
54.3
55.0
55.1
Implicit price
of fiber
(dollars
per kilogram)
3.47
3.48
3.48
3.62
3.67
3.68
aPresent discounted values were computed using the following economic parameters:
thirty year plant life, 4.74 percent real rate of discount, fourty-nine percent
effective tax rate, ninety-five percent plant utilization, and ten percent
investment tax credit.
9-87
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The increases in emissions control increase the price of fiber
produced by new facilities when moving from the baseline level of
control to Regulatory Alternative II for both Model Plants 4 and 5.
However, no further price increases result from the move from Regulatory
Alternative II level of control to Regulatory Alternative III level of
control. The output of Model Plant 4 is estimated to increase 0.3 percent
due to either of the regulatory alternatives; the output of Model
Plant 5 is estimated to increase 1,7 percent due to either of the
regulatory alternatives. Full cost impact absorption by producers
results in increases in the present value of costs of operation in all
cases except that of moving from Regulatory Alternative II to Regulatory
Alternative III with Model Plant 4. The present value cost increases
range from $2.6 million to $16.8 million.
The same qualifications mentioned with respect to the accuracy of
the acrylic and modacrylic implicit price and cost results also apply
to the results for cellulose acetate fibers. In addition, it should
be noted that the relative price of solvents has recently been rising
very rapidly. If the trend continues, the credits for additional
solvent recovery will grow faster than the costs of installing additional
recovery equipment, and cost savings or price reductions might result.
9.2.3.4 Capacity Projections Reconsidered. As discussed in
Section 9.2.2.4, there is some evidence that a discontinuous supply
function may characterize the synthetic fiber industry. To assist in
determining whether such considerations might adversely affect the
projections of new cellulose acetate capacity presented in Section 9.1.3.4,
the implicit prices calculated from the discounted cash flow analysis
for cellulose acetate were compared with the mid-1980 market prices of
these fibers. This comparison is presented below.
Prices
(dollars per kilogram)
Market
Model Plant 4
(cigarette filtration tow)
Model Plant 5
(textile fibers)
2.40
86
2.67-2.98
82
Implicit
3.47-3.48
3.62-3.68
9-88
-------
For cigarette filtration tow, the implicit prices are nearly
50 percent greater than the observed market price in mid-1980.
Additionally, the market price reported in March of 1982 for cigarette
87
filtration tow was $2.71-$2.76, still substantially below the implicit
price suggested by the model plant analysis. This divergence of
approximately one dollar per kilogram between mid-1980 market tow
prices and the implicit price required to make new plant construction
profitable at first glance suggests that new plants would not actually
be constructed at the rate projected above in Section 9.1.3.4.
In the past, manufacturers of cellulose acetate fibers have
converted cellulose acetate yarn and staple capacity to cigarette
filtration tow capacity, apparently due to increases in tow prices
that provided greater earnings opportunities than were available from
yarn or staple production. If firms were able to continue to convert
cellulose acetate yarn and staple capacity to filtration tow capacity,
the capacity shortfall for cigarette filtration tow could be met by
converted plants that would not fall under the NSPS, so long as emissions
did not increase and conversion costs were less than 50 percent of the
capital costs estimated for a new facility. A representative of
Tennessee Eastman reported that conversion of yarn facilities to tow
facilities had been accomplished previously in approximately one year,
and for less than 50 percent of estimated capital costs for a new
oo
facility. Economic theory suggests that producers will continue to
convert yarn and staple capacity to tow capacity if the price of tow
increases relative to the price of yarn. However, industry analysts
state that the cellulose acetate yarn market is currently stable and
that yarn capacity has already been converted to the extent that
QQ on
producers are willing to do so. *
Assuming that there will be no further conversion of capacity, as
industry suggests, the market price of cigarette filtration tow must
rise to approximately $3.47 per kilogram, before producers will build
new capacity, even at the baseline level of control.
Figure 9-2 depicts the hypothesized domestic market for cellulose
acetate filtration tow. Domestic demand for cellulose acetate filtration
tow is currently D D . The demand curve DQDo intersects the supply
9-89
-------
Price
Per
Kilogram
R, ($3.471
P0 ($2.40)
Quantity of Tow
Figure 9-2. Domestic Market for Cellulose Acetate Filtration Tow
9-90
-------
curve S S at quantity Q , which reflects that the industry is currently
operating at maximum capacity utilizaton, and at price PQ, equal to
$2.40 per. kilogram. Demand for cigarette filtration tow is highly
price inelastic, as reflected in the nearly vertical demand curve,
D D . The market price for tow will move to P,, equal to $3.47 per
o o *•
kilogram, only if demand shifts from DQDO to D-^D^.
The supply curve S S is depicted as a vertical line between
price P and price P,, reflecting perfectly inelastic supply of tow to
the domestc market between these two prices. Three assumptions are
required to characterize this segment of the supply curve in this
manner. First, as price moves from PQ to P^t domestic producers will
continue to export that amount of tow that they were exporting at
price P . Second, as price moves from PQ to Pp domestic cigarette
producers will continue to import the same amount of tow as they
imported at P . Third, domestic cigarette producers will not substitute
other materials for tow in cigarette production (i.e., paper or charcoal),
Given that demand is highly inelastic and that supply is perfectly
inelastic, little shift in demand is required to raise market price
from PQ ($2.40) to ?l ($3.47).
The elasticity of demand for cigarette filtration tow was estimated
by the EPA and indeed found to be highly inelastic. Elasticity of
demand refers to the percent change in the quantity demanded of a
product due to a 1 percent change in the price of that product. The
price elasticity for tow was derived from the price elasticity for
cigarettes (estimated to be -0.5)90 and the cost share of filter tow
in cigarettes (estimated by the EPA to be 0.015). Cigarette filtration
tow was estimated to have an elasticity of demand of -0.0075, that is,
a 1 percent change in its price would result in only a .0075 percent
change in the quantity of tow demanded.
Characterizing supply as perfectly inelastic between PQ and P-^
requires three assumptions, as mentioned above. The first assumption,
that cigarette producers will not substitute paper or charcoal filters
for cellulose acetate filtration tow, is supported by evidence (in the
Chemical Economic Handbook's Marketing Research Report on Cellulose
Acetate and Triacetate Fibers) that cigarette smokers prefer the taste
9-91
-------
of cellulose acetate filters to that of paper filters, and that charcoal
filters have decreased in popularity in recent years.
The other two assumptions, regarding foreign trade effects, are
that neither the quantity of tow exported (approximately a third of
domestic production) nor the quantity of tow imported (currently none)
will be affected by the rising price of domestic tow. It is likely
that increases in the price of domestic tow will have some effect upon
these two components of foreign trade. However, these effects were
not incorporated due to the lack of necessary data and the scope of
this analysis.
Using these supply assumptions, the demand elasticity estimates,
and the projected rate of growth for cigarette filtration tow, the EPA
estimated the time it would take for demand to shift from DQDo to
D-,D-,, and found this time interval to be less than one month. The
uncertainty regarding the supply assumptions and demand elasticity and
rate of growth estimates brings into question the accuracy of this
estimate of the time required for the demand shift. However, even
given this uncertainty, it is reasonable to conclude that the time
interval will not be of such great duration as to significantly delay
construction of new plants.
Turning to the market for cellulose acetate textile fibers, the
implicit price is substantially greater than the market price for
these fibers. Given the estimated 1982-1987 capacity shortfall of 7.3
to 7.8 gigagrams, and the contention that industry would be inclined
to build in plant unit capacities of 22.7 gigagrams, the EPA has
concluded that there will be no additions to cellulose acetate yarn
capacity in the period 1982-1987. This conclusion is qualitatively
supported by an analyst within the cellulose acetate yarn industry who
characterizes the growth in demand for these fibers as stable.
9.3 POTENTIAL SOCIOECONOMIC AND INFLATIONARY IMPACTS
Executive Order 12291 requires that the inflationary impacts of
major legislative proposals, regulations, and rules be evaluated. The
proposed NSPS would be considered a major action (thus requiring the
preparation of a Regulatory Impact Analysis) if any of the following
criteria apply:
9-92
-------
curve S S at quantity QQ, which reflects that the industry is currently
operating at maximum capacity utilizaton, and at price PQ, equal to
$2.40 per. kilogram. Demand for cigarette filtration tow is highly
price inelastic, as reflected in the nearly vertical demand curve,
D D . The market price for tow will move to P,, equal to $3.47 per
o o -1-
kilogram, only if demand shifts from D0DQ to DjDp
The supply curve S S is depicted as a vertical line between
price P and price P,, reflecting perfectly inelastic supply of tow to
the domestc market between these two prices. Three assumptions are
required to characterize this segment of the supply curve in this
manner. First, as price moves from PQ to Pp domestic producers will
continue to export that amount of tow that they were exporting at
price P . Second, as price moves from PQ to Pp domestic cigarette
producers will continue to import the same amount of tow as they
imported at P . Third, domestic cigarette producers will not substitute
other materials for tow in cigarette production (i.e., paper or charcoal),
Given that demand is highly inelastic and that supply is perfectly
inelastic, little shift in demand is required to raise market price
from PQ ($2.40) to PI ($3.47).
The elasticity of demand for cigarette filtration tow was estimated
by the EPA and indeed found to be highly inelastic. Elasticity of
demand refers to the percent change in the quantity demanded of a
product due to a 1 percent change in the price of that product. The
price elasticity for tow was derived from the price elasticity for
cigarettes (estimated to be -0.5)90 and the cost share of filter tow
in cigarettes (estimated by the EPA to be 0.015). Cigarette filtration
tow was estimated to have an elasticity of demand of -0.0075, that is,
a 1 percent change in its price would result in only a .0075 percent
change in the quantity of tow demanded.
Characterizing supply as perfectly inelastic between PQ and P-^
requires three assumptions, as mentioned above. The first assumption,
that cigarette producers will not substitute paper or charcoal filters
for cellulose acetate filtration tow, is supported by evidence (in the
Chemical Economic Handbook's Marketing Research Report on Cellulose
Acetate and Triacetate Fibers) that cigarette smokers prefer the taste
9-91
-------
of cellulose acetate filters to that of paper filters, and that charcoal
filters have decreased in popularity in recent years.
The .other two assumptions, regarding foreign trade effects, are
that neither the quantity of tow exported (approximately a third of
domestic production) nor the quantity of tow imported (currently none)
will be affected by the rising price of domestic tow. It is likely
that increases in the price of domestic tow will have some effect upon
these two components of foreign trade. However, these effects were
not incorporated due to the lack of necessary data and the scope of
this analysis.
Using these supply assumptions, the demand elasticity estimates,
and the projected rate of growth for cigarette filtration tow, the EPA
estimated the time it would take for demand to shift from D0DQ to
DjD,, and found this time interval to be less than one month. The
uncertainty regarding the supply assumptions and demand elasticity and
rate of growth estimates brings into question the accuracy of this
estimate of the time required for the demand shift. However, even
given this uncertainty, it is reasonable to conclude that the time
interval will not be of such great duration as to significantly delay
construction of new plants.
Turning to the market for cellulose acetate textile fibers, the
implicit price is substantially greater than the market price for
these fibers. Given the estimated 1982-1987 capacity shortfall of 7.3
to 7.8 gigagrams, and the contention that industry would be inclined
to build in plant unit capacities of 22.7 gigagrams, the EPA has
concluded that there will be no additions to cellulose acetate yarn
capacity in the period 1982-1987. This conclusion is qualitatively
supported by an analyst within the cellulose acetate yarn industry who
characterizes the growth in demand for these fibers as stable.
9.3 POTENTIAL SOCIOECONOMIC AND INFLATIONARY IMPACTS
Executive Order 12291 requires that the inflationary impacts of
major legislative proposals, regulations, and rules be evaluated,, The
proposed NSPS would be considered a major action (thus requiring the
preparation of a Regulatory Impact Analysis) if any of the following
criteria apply:
9-92
-------
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ABBREVIATIONS USED IN THE FIBERS INDUSTRY
Abbreviations/Monomers
AN - Acrylonitrile, vinyl cyanide H2C = CH - C = N
AMS - Alpha Methyl Styrene, CgH5 - C (CH3) = CH2
BD - Butadiene, Divinyl, HgC = CH - CH = CH2
MA - Methyl Acrylate, H2C CH - COOCHj
MMA - Methyl Methacrylate, HgC = C(CH3) - COOCH3
STY - Styrene, vinyl benzene, CgHg - CH CH2
VA - Vinyl Acetate, CH3 - COO - CH = CH2
VC - Vinyl idene Chloride, CH2 = C - C12
2VP - 2 Vinyl Pyrridine
- N - CH = CH
VC - Vinyl chloride, CH2 = CH - Cl
2. Abbreviations/Polymers
A8S - Acrylonitrile Butadiene Styrene resin
NBR - Nitrile Butadiene Rubber elastomer
PAN - Polyacrylonitrile
SAN - Styrene Acrylonitrile copolyiner
SBR - Styrene Butadiene Rubber elastomer
PBR - Polybutadiene Rubber elastomer
3. Abbreviations/Solvents
AC
STC
ZC1
DMAC
DMF
Acetone, CH
Sodium Thiocyahate, NaSCN
Zinc chloride, ZnCl.-,
DiMethyl Acetamide, CH3CON(CN3)2
D1Methyl Fomiamide, HCON(CH3)2
MW 53
MW 118
MW 54'
MW 86
MW 100
MW 104
MW 86
F',l 97
MW 105
MW 62.5
F-ll
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TECHNICAL REPORT DATA
(Please read Instructions on the reverse before completing)
I, REPORT NO.
EPA-450/3-82-011a
2.
3. RECIPIENT'S ACCESSION-NO.
4. TITLE AND SUBTITLE
Synthetic Fiber Production Facilities- Background
Information for Proposed Standards
5. REPORT DATE
October 1982
6. PERFORMING ORGANIZATION CODE
7. AUTHOR(S)
8. PERFORMING ORGANIZATION REPORT NO.
9. PERFORMING ORGANIZATION NAME AND ADDRESS
Office of Air Quality Planning and Standards
Environmental Protection Agency
Research Triangle Park, North Carolina 27711
10. PROGRAM ELEMENT NO.
11. CONTRACT/GRANT NO.
68-02-3060 ;
12. SPONSORING AGENCY NAME AND ADDRESS
DAA for Air Quality Planning and Standards
Office of Air, Noise, and Radiation
U. S. Environmental Protection Agency
Research Triangle Park, North Carolina 27711
13. TYPE OF REPORT AND PERIOD COVERED
Final
14. SPONSORING AGENCY CODE
EPA/200/04
15. SUPPLEMENTARY NOTES
10. ABSTRACT
Standards of performance to control emissions of volatile organic
compounds (VOC) from new, modified, and reconstructed synthetic fiber
production facilities are being proposed under section 111 of the Clean
Air Act. This document contains information on the background and authority,
regulatory alternatives considered, and environmental arid economic impacts
of the regulatory alternatives.
17.
KEY WORDS AND DOCUMENT ANALYSIS
DESCRIPTORS
b.lDENTIFIERS/OPEN ENDED TERMS C. COS AT I Field/Group
Air pollution
Pollution control
Standards of performance
Industrial processes
Synthetic fibers
Volatile organic compounds
Air Pollution Control
Organic Vapors.
Stationary Sources
13 B
(VOC)
18. DISTRIBUTION STATEMENT
Unlimited
19. SECURITY CLASS (ThisReport)
Unclassified
21. NO. OF PAGES
396
2O. SECURITY CLASS (This page)
Unclassified
22. PRICE
EPA Form 2220-1 (9-73)
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