-------
If 20% more fly ash is sold, the difference on the NEP balance sheet is about $120K/yr. NEP
has a corporate goal to recycle 100% of the fly ash generated by its two coal-fired stations by the
year 2000.
Another consequence of ammonia slip at Salem Harbor is increased risk of ammonium bisulfate
deposits on the tubular air heater. Such deposits could reduce heat transfer effectiveness in the air
heater and eventually lead to pluggage and downtime to water wash the equipment. If only one
day of unscheduled downtime is avoided, about $45K of replacement power could be avoided.
Total savings could be in the range of $200K/yr at Salem Harbor #2 alone. NEP has also installed
SNCR along with low-NOx burners on units #1 and #3 at the station. Better SNCR performance
could allow these units the flexibility to tune their burners for higher NOX and lower unburned
carbon in order to maximize flyash sales. Total savings for all three boilers at Salem Harbor
(325 MW) could be well over $500K/yr. The results of this project will help determine the
viability of enhanced SNCR as a compliance strategy at this station.
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COMMERCIAL APPLICATION OF UREA SNCR FOR NOx RACT COMPLIANCE
ON A 112 MWe PULVERIZED COAL BOILER
by
James E. Staudt, Ph.D.
Robert P. Casill, P.E.
Research-Cottrell
Thomas S. Tsai
Leonard J. Ariagno
Eastern Utilities
Abstract
Montaup Electric Company, a subsidiary of Eastern Utilities Associates, operates a
tangentially-fired pulverized coal boiler at its Somerset, MA generating station. NOx
emissions from the 112 MWe Montaup boiler #8 must be reduced from their
uncontrolled levels in order to comply with the Reasonably Available Control
Technology (RACT) requirements promulgated by the Commonwealth of Massachusetts.
According to RACT, NOx emissions from the unit must not exceed 0.38 Ib./MMBTU
when firing coal or 0.25 Ib./MMBTU when firing oil.
For reduction of NOx emissions from Montaup boiler #8, combustion controls and flue
gas treatment were considered. Montaup Electric chose Selective Non-Catalytic
Reduction (SNCR) technology as its primary means of reducing NOx from baseline
levels to the levels required for RACT compliance. The SNCR technology operates by
injection of controlled amounts of aqueous urea into the furnace to reduce the NOx to
nitrogen, water and carbon dioxide. Total project scope included design engineering,
equipment supply, installation, and system startup. Optimization and startup of the
system were completed in early March. Startup testing demonstrated that the system can
achieve compliance levels across the load range 35% to 100% MCR while maintaining
ammonia slip at about 10 ppm or less. This paper will describe the system provided to
Montaup Electric and will discuss the results of startup and optimization testing.
Submitted to: EPRI/EPA 1995 Joint Symposium on Stationary Combustion NOx
Control, Kansas City, Missouri, May 16-19, 1995.
-------
Background
Montaup Electric Company operates a 112 MWe boiler at its Somerset, MA Generating
Station. Boiler #8 began operation in 1959. It is a natural circulation, reheat, single-
drum radiant boiler with a dry bottom that is rated at 800,000 Ibs/hr steam flow at the
superheater outlet at 1,925 psig and 1,000°F. The furnace has four corners and four
levels of tilting, tangentially fired coal buckets. Between the four coal buckets in each
corner are three oil guns. The fuel for the boiler was changed from coal to oil in the
early 1970's, and in 1984 the boiler was retrofit to operate primarily on coal. A
Continuous Emission Monitoring System (CEMS) was recently installed on the boiler,
and a new Distributed Control System (DCS) is planned for installation in April and
May of this year. Plans are to maintain boiler #8 in operation well beyond the year
2000.
Boiler #8 operates on dispatch typically in a load following mode. During the day and
during other high demand periods the boiler operates at full capacity. In the evening
and on weekends the boiler load is frequently reduced to 35% to 55% MCR.
Maintaining boiler #8 within environmental compliance under this wide range of
operating conditions is, therefore, of critical importance.
In the Commonwealth of Massachusetts, Reasonably Available Control Technology
(RACT) for control of NOx from tangentially-fired utility boilers is defined as
compliance with the following emissions performance levels:
Fuel Emissions Level (24 hour average by CEMS)
Coal 0.38 Ib/MMBTU
Oil 0.25 Ib/MMBTU
Coal + Oil Weighted average of above two values
Under some conditions, particularly at part loads, boiler #8 cofires oil and coal. On an
annual basis about 90% of the thermal input is from coal. Uncontrolled NOx levels
measured from boiler #8 during temperature mapping and more recently during SNCR
system initial optimization testing are shown in Figure 1 as a function of load. As shown
in Figure 1, at part load conditions NOx levels can be much greater than those at full
load conditions due to the increased excess air levels that are necessary to maintain
reheat and superheat temperatures at their optimum level. Manipulation of furnace air
distribution enables some reduction of uncontrolled NOx. Simulated Over Fire Air
(SOFA), performed during temperature testing in December 1993 by feeding coal
through only the lower three coal buckets, produced the lowest NOx levels. However,
the NOx reduction possible in this manner alone is not adequate to achieve the NOx
emissions levels required in Massachusetts for compliance with RACT. Additional NOx
control measures are necessary.
-------
To comply with RACT, Montaup Electric evaluated several technologies, including low
NOx burners, Selective Non-Catalytic Reduction (SNCR) and Selective Catalytic
Reduction (SCR). Capital and operating cost, and performance guarantees over the
entire load range were the key issues in selecting a technology for RACT compliance.
SNCR using aqueous urea solution was selected by Eastern Utilities for RACT
compliance on Montaup Electric's boiler #8. Research-Cottrell supplied all engineering,
equipment, installation, and startup services needed for implementation of the SNCR
system, including initial furnace temperature mapping.
System Description
The SNCR system provided to Montaup Electric included reagent storage, all pumping
systems, and twenty eight wall-mounted injectors arranged at four elevations in the
furnace as in Figure 2. The four zones of injection are necessary in order to achieve
NOx reduction over the operating range of 35% to 100% MCR when firing coal and/or
No. 6 fuel oil. Of the twenty eight injectors, nineteen utilized existing furnace
penetrations. Nine new penetrations were installed to accommodate the injectors.
Major pieces of equipment are schematically displayed in Figure 3 and include: a 20,000
gallon storage tank for outdoor storage of 50% by weight aqueous urea solution; a
circulation loop with circulation pumps and in-line heater to maintain the temperature of
the concentrated urea solution above the urea crystallization temperature; a chemical
metering and mixing system that provides a measured amount of reagent to the injection
levels at a prescribed pressure; distribution modules that modulate liquid flowrate and
atomizing air pressure to the individual injectors; two-fluid, air-atomized injectors that
automatically retract on zones 1 and 2 when these zones are not in operation; and a
control system composed of a Programmable Logic Controller, computer interface, local
control panels that enable local manual control of equipment, and associated valves and
instrumentation. Total project duration, from receipt of order to completion of startup
and optimization, was about eleven months. Installation of the boiler penetrations was
achieved during an outage of about two weeks.
Control of the system is feed-forward based upon inputs of steam flow (or oil flow) and
mill configuration. From these signals the PLC will determine which injectors are
operated and the maximum and minimum reagent that can be pumped to each injection
level. A NOx feedback signal from the CEMS to the PLC enables control of the reagent
flowrate within this range to minimize overcontrol or undercontrol. The operator can
adjust the setpoints in the control system as he sees fit.
Results Of Initial Start Up and Optimization Testing
Initial startup and optimization testing was performed to confirm the operability of the
SNCR system and to establish the setpoints for all system components, including injector
atomization parameters and the control system look-up table set points. During this
period the system performance was characterized with respect to: 1) NOx reduction; 2)
ammonia slip; and 3) reagent consumption. NOx was measured by the plant's CEMS.
-------
Ammonia slip was determined by wet chemical means. Flue gas samples from
downstream of the economizer were drawn through a known volume of sulfuric acid
solution. The solution was analyzed for concentration of ammonia ion using an
ammonia ion selective electrode. By this method ammonia concentration in the flue gas
could be determined. Samples were taken by Research-Cottrell and an independent
company contracted by Montaup Electric. Correspondence between independent
measurements was generally very good.
Reagent treatment rate in this paper is expressed in terms of gallons per hour of 50%
aqueous urea solution and in terms of Normalized Stoichiometric Ratio (NSR). NSR is
the ratio of the actual Stoichiometric ratio (of urea to uncontrolled NOx) to the
Stoichiometric ratio for theoretically 100% NOx reduction and 100% chemical utilization.
For urea, NSR is equal to:
NSR = (moles of urea/moles of uncontrolled NOx) x 2
Full Load Testing
At 100% MCR conditions, NOx reduction was achieved through injection of reagent into
the two uppermost injection zones (zones #3 and #4). Full load optimization testing
results, shown in Figure 4 as ammonia slip versus NOx reduction, indicate that at full
load conditions NOx reductions in excess of 50% may result in ammonia slip in excess of
10 ppm. Figure 5 shows the results of testing at full load with variation of treatment rate
and a constant 1 to 2 bias in reagent flow between zones 3 and 4, respectively. The
testing demonstrated that NOx compliance (at or below 0.38 Ib/MMBTU) could be
achieved with less than 10 ppm of ammonia slip.
Mid-Load Testing
Boiler #8 operates periodically between 85 and 105 MWe and very little between 60 and
85 MWe. Normally the boiler passes through these load levels during early morning
load ramp up to full load or during evening load ramp down to about 35-60 MWe (net).
Although the boiler operates less often in these middle loads, the high baseline NOx
levels under these load conditions determined some of the design limitations of the
SNCR system provided to Montaup Electric.
At 95 MWe, uncontrolled NOx levels can exceed 0.90 Ib/MMBTU. In terms of total
NOx emissions, this is the worst case condition for the boiler. However, baseline NOx
levels can be reduced by adjustment of furnace air distribution. Figure 6 shows the
results of testing at 95 MWe with in initial NOx of 0.63 Ib/MMBTU. Testing
demonstrated that NOx can be reduced to compliance levels with roughly 10 ppm or less
of ammonia slip.
-------
In order to test the limits of the SNCR system and to demonstrate the economic benefits
of reducing baseline NOx through combustion air adjustment, testing of the SNCR
system was performed at high NOx levels (0.94 Ib/MMBTU) and 95 MWe. Testing
showed that under these conditions NOx could not be reduced by the SNCR system to
below 0.38 due to the high chemical flowrates required, which exceeded pump capacity.
These results were expected since the system provided to Montaup Electric was not
designed to accommodate this extreme case. In any event, operation in this manner is
uneconomical due to the very high chemical consumption. Reagent chemical costs
ranged about $0.80-$ 1.00 per gallon during this testing. However, as shown in Figure 7,
at the lower baseline NOx level of 0.63 Ib/MMBTU, chemical consumptions can be
greatly reduced and compliance more economically achieved.
At 85 MWe, baseline NOx emissions during testing ranged from about 0.90-0.98
Ib/MMBTU. This is the lowest load condition on Boiler #8 where only coal is fired.
Below 85 MWe, Montaup Electric usually co-fires some oil with the coal. The results of
testing at 85 MWe are shown in Figure 8. Testing showed that NOx emissions below
0.38 Ib/MMBTU could be achieved with less than 5 ppm ammonia slip by injection
through zone 3 and 4 injectors. Injection of reagent through zone 2 and 3 injectors could
not achieve adequate NOx reduction because of the higher temperatures in these zones
at this load condition.
Law Load Testing
The results of SNCR testing at 40 MWe are shown in Figure 9. NOx emissions were
reduced to nearly 0.30 Ib/MMBTU while maintaining below 10 ppm ammonia slip with
reagent injection through zones 1 and 2. Reduction to below 0.30 Ib/MMBTU was
possible; however, ammonia slip increased above 10 ppm. Had NOx levels below 0.30
Ib/MMBTU been necessary under this load condition, it could have been provided for
through design of a different injector configuration. Figure 8 also demonstrates the
benefit of independent zone control with injection into two zones. Injection through
zone 2 injectors alone produced high ammonia slip (over 20 ppm - the highest ammonia
slip measured during the test period) with no advantage in NOx reduction. Injection into
zones 1 and 2 produced lower ammonia slip with good NOx reduction.
Load Following
Because Montaup Electric boiler #8 operates over a wide load range, the SNCR system
was designed to follow load and maintain the unit in compliance over the full load range.
The boiler, in fact, spends very little time at intermediate loads. Typically daytime
operation is at or near 100% MCR. At times that the unit is not operating at or near
full load, it is operating in the range of about 35%-55% MCR. Since the unit normally
passes through intermediate loads and these are the loads where NOx is most difficult to
control on this unit, this is a challenging application for a control system. The control
system must very quickly respond to a situation that initially requires increasing reagent
injection rates while changing injection levels, and then requires decreasing injection
rates while injection levels continue to change.
-------
In the short time that Montaup Electric has operated the SNCR system, the SNCR
system's response to load changes has been observed. From this limited experience, the
system seems to take about 30 minutes to fully adjust to a major load transient, as shown
in Figure 10. This, however, is expected to be improved through adjustment of control
system time constants and could be further improved, if needed, by use of in-duct NOx
analyzers for feedback. Several minutes pass before the stack CEMS will indicate a
change in NOx within the furnace, which results in a lag in the SNCR system response.
In-duct NOx analyzers would reduce that lag time to seconds. Nonetheless, although
NOx may pass above the NOx setpoint for a short time during the transient, the system
consistently stabilizes at or below compliance levels. Figure 10 also shows a transient in
the SNCR system while the CEMS was taken out of service, which exacerbated the NOx
excursion during the load transient. The SNCR control system provided to Montaup
Electric has a feature to properly accommodate for such situations; however, it will not
be in operation until after Montaup Electric completes its DCS installation this spring.
With this feature enabled and with additional operating experience, Montaup Electric
operators can adjust the SNCR system controls to minimize any NOx excursions during
transients.
Carbon Monoxide Emissions
Carbon Monoxide (CO) emissions can potentially increase as a result of SNCR with
urea. However, noticeable increases in CO emissions were not observed during the start
up and optimization of the SNCR system.
Economics
The fully installed capital cost of this SNCR system is in the range of $15-$ 16 per KWe.
This cost includes a technology license fee which is a significant portion of this total cost.
Were Montaup Electric a member of E.P.R.I., the license fee would have been
substantially less.
Under full load conditions it was demonstrated that compliance could be achieved with
roughly 150 gallons per hour of reagent. Using a price of $0.80-$ 1.00 per gallon, this
equates to a reagent cost of $700-$880 per ton of NOx removed, or about 1 1 to 13 mils
per KW-hr.
-------
Summary
Start up and optimization of the SNCR system at Eastern Utilities' 112 MWe Montaup
Electric Boiler #8 demonstrated that the system is capable of reducing NOx to below
Massachusetts RACT compliance levels over the load range of 35% to 100% MCR.
Over this load range ammonia slip remained at or below 10 ppm. Operation of the
system also demonstrated the economic benefits of minimizing baseline NOx to minimize
reagent consumption. Montaup Electric plans to incorporate automated combustion
controls that will reduce their baseline NOx and enable operation of the SNCR system
under the most economical conditions.
While experience with SNCR operation during load changes is limited at this time, the
control system provided has demonstrated that it can follow a load change and adjust
SNCR system operation to bring the NOx emissions in compliance at the new load.
Although a transient in NOx emissions may occur for a few minutes while the SNCR
system adjusts to the new condition, the system consistently brings NOx emissions into
compliance levels. System response of the SNCR system will be improved through
operator experience and adjustment of system control parameters, thereby minimizing
these transients.
-------
Figure 1, Montaup Electric
Baseline NOX vs. Load
p
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0 30 40 50 60 70 80 90 100 110 120
Load (MWe)
12/93
Figure 2
Boiler #8 and Urea Injector Locations
-------
FigureS
Process Flow Diagram of SNCR System
Circulation Pump
Distribution
Modules
Figure 4, Montaup Electric
Full Load
NH3 slip vs NOX Reduction
Each Zone
Injector
To Each Zone II
Injector
To Each Zone III
Injector
To Each Zone N
Injector
1
ex
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NOX Reduction
-------
Figure 5, Montaup Electric
Boiler #8
Full Load Test
ffl
X
o
0.90
0.80
0.70
0.60
0.50
0.40
0.30
0.20
0.10
ft
""•"•••••••.,,
0 0.2 0.
""""••-••••••..„
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_
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.0 1.2 1.4 1.6
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70
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Figure 6, Montaup Electric
Boiler #8, 95 MWe
NOX NH3 slip vs NSR
u./u
.60
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.j(j
A AC\
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A 9A
0 10
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0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4 2.6
NSR
• NOx (Ib/MMBTU) | + NH3 slip
/O
60
50
40
§
30
20
1 A
10
(\
u
-------
NOX
(Ib/MMBTU)
Figure 7, Montaup Electric
NOX vs. Reagent Flowrate
95 MWe, NOx Baseline 0.93, 0.63
1.00
A OA
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'"---++
o
50 100 150 200 250
Reagent Flowrate (gph)
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0.93
I + 0.63
350
ra
1.00
0.90
0.80
0.70
g 0.60
0.50
0.40
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Figure 8, Montaup Electric
Boiler #8, 85 MWe
NOX and NH3 slipvs NSR, vary injection zones
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-•-•••*,
2&3
2 & 3
• -••-.
'•••••••••-.,, 3 & 4
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a
4 £
05
CO
-------
Figure 9, Montaup Electric
Boiler #8,40 MWe
NOX and NH3 vs NSR, zones 1&2 or 2 only
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+ NHSslip
Figure 10, SNCR System Response to Load Change
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90
80
70
0) 60
* 50
c
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0 40
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& 30
20
10
0
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90 80 70 60 50 40
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30 20 10 0
100
90
80
70
60
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50
40
30
20
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Time (in Minutes)
-------
AMMONIA ABSORPTION ON COAL AND OIL FLY ASHES*
L. J. Muzio, E. N. Kim, M. A. McVickar, G. C. Quartucy
Fossil Energy Research Corp.
Laguna Hills, California 92653
M. McElroy
EPT, Inc.
Menlo Park, California 94025
P. Winegar
N. Y. Power Authority
(ESEERCO)
New York, New York 10019
Abstract
Ammonia and urea based post-combustion NOX control technologies (e.g., SNCR, SCR) are
becoming more common as utilities strive to meet more stringent NOX emission regulations.
One issue associated with these technologies is the fate of ammonia slip. A portion of the NH3
slip will be absorbed by the fly ash. Depending on the concentrations of ammonia in the ash,
this may pose odor problems while handling the ash, and impact the disposal and marketability
of the ash.
This paper presents the results of a bench-scale study conducted to characterize NH3 absorption
by fly ash. The experiment investigated NH3 absorption as a function of ash type (four coal
ashes, two oil ashes), exposure time, temperature, and NH3 concentration.
Introduction
Since the passage of the 1990 Clean Air Act Amendments, post-combustion NOX control
technologies are becoming more important in compliance strategies. These post-combustion
NOX control technologies include Selective Non-Catalytic NOX Reduction (SNCR) and Selective
Catalytic NOX Reduction (SCR). One byproduct of these processes is ammonia slip (i.e.,
unreacted ammonia which is emitted with the combustion products)1.
"The work presented in this paper was funded by the Empire State Electric Energy
Research Corporation (ESEERCO).
-------
One issue that has received little research attention to date, but has become increasingly
recognized as a problem in full-scale applications, is the absorption of NH3 by either coal or oil
ash. The absorption of unreacted NH3 from SNCR processes by ash generated from the
combustion of oil or coal can have implications for plant operations. First, personnel handling
the ash can be subjected to NH3 if the ammonia off-gases from the ash; this impacts how the ash
must be handled by site personnel. Secondly, the marketability or disposal of the ash may be
impacted.
From the personnel exposure standpoint, NH3 can be released if the ash becomes wet and the
resulting ash pH becomes basic. Figure 1 shows the equilibrium between ammonia (gas) and
ammonium ion in an aqueous solution as a function of pH2. Below a pH of 7, the ammonia will
remain in the aqueous phase. As the pH is increased above 7, the balance begins to shift to the
gaseous phase. At a pH of just over 9 the equilibrium shifts, driving a substantial amount of the
ammonia to the gas phase. All of the ammonia is in the gas phase by the time the pH increases
to 11.
Little information is available regarding the amount of NH3 that will be absorbed by fly ash.
Most of this information is from full-scale applications where the parameters controlling the
amount of NH3 absorption are difficult to delineate. Thus, there is a need to develop an
understanding of the factors that control ash ammonia absorption, and to determine what, if
anything, can be done to limit the ammonia absorption. Examples of variables to be evaluated
include:
• Contact time — if temperature is important, then operating changes which reduce ash
contact time (increasing baghouse cleaning or ESP rapping frequency) could reduce
ammonia ash concentration.
• Temperature — if temperature is important, then hopper temperature could be regulated
by using steam coil heaters or reducing the air preheater surface area.
Figure 2 shows parametrically how the ash ammonia concentration will vary with the exhaust
gas ammonia concentration and the percentage absorbed (Figure 2 assumes a 10% ash coal).
These data show, that for 10 ppm NH3 slip and a 50 percent absorption, the ash ammonia
concentration would be over 400 ppm. These data will be useful later in evaluating the behavior
of different ashes.
In recognition of the need for a basic understanding of ammonia absorption by coal and oil ash
produced in utility boilers, the Empire State Electric Energy Research Corporation (ESEERCO)
sponsored this laboratory study. The testing was performed by Fossil Energy Research
Corporation (FERCo) under contract to Electric Power Technologies, Inc. (EPT). This work is
part of a larger ESEERCO laboratory research program investigating issues related to the SNCR
process.
-------
Objectives
The primary objectives of this bench scale study were to develop a general understanding of ash
ammonia absorption and determine to what extent, if any, it is related to ash type. It should be
noted that there are two mechanisms by which ammonia can be associated with fly ash. As the
combustion products cool through the air preheater, NH3/SO3 reactions will take place. The
resulting ammonia bisulfate, or sulfates, can become associated with the ash. Secondly, the
gaseous ammonia can be directly absorbed by the ash. This study dealt with this latter
mechanism (i.e., the direct absorption of NH3 on fly ash).
Experimental Apparatus
The experiments were performed using a bench-scale fixed bed apparatus. A schematic of the
apparatus is shown in Figure 3. The system included compressed gas cylinders to generate
synthetic flue gas, a humidification system and a heated oven for exposing the ash sample to the
synthetic flue gas at fixed temperatures and times.
The simulated flue gas was blended from compressed gas cylinders of CO2, O2, N2, SO2 and
NH3. The CO2, O2 and N2 were mixed together first and then passed through a controlled
temperature humidifier. Upon leaving the humidifier, SO2 and NH3 were doped into the gas
supply leading to the oven containing the ash sample. The supply line was heat traced to avoid
condensation of water and ammonia and heat the mixture to the desired dry bulb temperature.
After exposure to the simulated flue gas for a specified amount of time, the ash sample was
removed from the oven. The ash sample was added to a container containing 200 ml of dilute
sulfuric acid; the dissolved ammonia content of the sample was then determined with a
calibrated specific ion electrode. The NH3 concentration of the sample was then normalized to
the initial weight of the ash sample, and the ammonia content reported as a weight ppm.
It should be noted here that the bench-scale approach used for these experiments differed
somewhat from the actual gas/solid contacting in an ESP or fabric filter. The bench-scale
apparatus probably provides more gas/solid contacting than occurs in an ESP, but should be a
reasonable simulation of the gas/solid contacting process in a fabric filter.
Test Matrix and Ash Analysis
The synthetic flue gas used for these experiments had the following nominal composition:
H,O: 8%
CO,: 14 %
O2: 3 %
SO,: 1500 ppm
This gas composition was chosen to be reasonably representative of a coal- or oil-fired boiler
which burned a 2 to 2.5% sulfur fuel. The 1500 ppm SO2 level was selected as a worst case
scenario. The scope of testing is shown below.
-------
Ash type : 2 oil ashes, 4 coal ashes
Temperature: 250-325°F
NH3 concentration : 0-20 ppm
NHj/Ash exposure time : 0-60 minutes
Since this study addressed the direct absorption of NH3 on fly ash, not NH3/SO3 reactions, SO3
was not present in the simulated flue gas.
The primary variable during these tests was the contact time between the ash samples and the
NH3 laden flue gas stream. Exposure times ranged from nominally two minutes to one hour.
For each ash, NH3 absorption was determined at temperatures ranging between 250 and 325 °F, a
representative range of utility boiler air heater outlet temperatures. The simulated flue gas
contained 10 ppm of NH3. This NH3 slip value was selected as representative of potential
regulatory and/or operational limits. In addition, a single case was evaluated at an NH3 slip level
of 20 ppm to assess the impact of the flue gas NH3 concentration.
The ashes were selected to be representative of oil and coal ashes typically found in New York
State. In addition, ash samples were obtained from Public Service Company of Colorado's
Arapahoe Station (where a low-sulfur, western, bituminous coal is burned) and New England
Power's Salem Harbor Station (where a low-sulfur South American coal was burned). A total of
six ashes were obtained for this study; their source and properties are listed in Table 1.
Table 1
Ash Source and Nominal Properties
Utility
Niagara Mohawk
Niagara Mohawk
Long Island Lighting
Rochester Gas & Electric
Public Service Co. of Colorado
New England Power
Unit
Oswego 6
Huntley
Port Jefferson
Russel 4
Arapahoe 4
Salem Harbor
Fuel
Type
Oil
Coal
Oil
Coal
Coal
Coal
Fuel
Sulfur,
1.5
n/a
1.0
n/a
0.5
0.7
Ash Collection
Location
Baghouse Hopper
n/a
ESP Hopper
n/a
Baghouse Hopper
ESP Hopper
In order to attempt a correlation between NH3 absorption and ash characteristics, the following
tests were performed on each ash: BET (surface area, m2/g), SO4 (wt%), pH, and carbon (wt%).
The results from these tests are summarized in Table 2 and discussed below.
Ash surface area was measured using a standard single point BET technique. The two oil ashes
had comparable surface areas-4.11 m2/g for Oswego and 5.72 m2/g for Port Jefferson.
-------
However, the coal ashes exhibited a wide range in surface areas from 1.2 m2/g (Rochester) to
15.3 m2/g (Salem Harbor).
Table 2
Ash Characteristics
Ash
Source
Oswego, NIMO
Port Jefferson, LILCO
Huntley, NIMO
Russel, RG&E
Salem Harbor, NEP
Arapahoe, PSCC
Ash
Type
Oil
Oil
Coal
Coal
Coal
Coal
BET
mA2/g
4.11
5.72
8.08
1.23
15.33
12.79
S04
wt%
33.98
24.27
0.78
0.66
0.49
0.37
pH*
8.6
3.4
7.7
9.8
10.1
10.0
Carbon
%
4.48
6.93
10.81
1.17
37.82
6.16
For 0.25 grams of ash sample in 200 ml of distilled water.
The pH of the ash was determined by adding varying amounts of ash to 200 ml of distilled
water. Figure 4 shows how the ash to water ratio affected the resulting pH. As can be seen, the
oil ash from Port Jefferson (LILCO) was highly acidic, whereas the oil ash from
Oswego (NIMO) was alkaline. This suggests a fairly high amount of MgO in the Oswego ash,
which was expected since MgO is used both as a fuel oil additive and also injected at the air
heater inlet.
Ash aliquots were also sent to an independent laboratory for sulfate and carbon analyses. The
sulfate levels in the oil ashes were essentially an order of magnitude higher than those in the coal
ashes. The Oswego and Port Jefferson ashes had 33.98 and 24.27 wt% sulfate, respectively;
whereas the coal ashes all had sulfate levels below 1% (see Table 2).
Ash carbon levels typically ranged between 1 and 11%, with the exception of the Salem Harbor
ashes. The carbon content in the Salem Harbor, at 38%, was much higher. At the time the ash
sample was obtained from Salem Harbor, the unit was not being operated under normal
conditions according to plant personnel; consequently, the carbon level in the ash sample used
during this study may not be typical of Salem Harbor. However, with its significantly higher
carbon level, this ash is interesting because it allows for the evaluation of NH3 absorption during
atypical boiler operation. Note: the carbon levels in the oil ashes were relatively low; it is not
uncommon to see oil ashes with carbon contents ^50%.
Test Results
In Figures 5a through 5c, the NH3 absorbed by each ash is plotted as a function of exposure time
(up to one hour) to synthetic flue gas with 10 ppm NH3 at temperatures of 250, 300 and 325°F,
-------
respectively. A large difference between the oil ashes and coal ashes is apparent. At all of the
temperatures evaluated, the amount of NH3 absorbed by the oil ashes (Oswego and Port
Jefferson) continued to increase linearly with time. After one hour of exposure, the absorbed
NH3 levels for the oil ashes varied between nominally 2000 and 3000 ppm. In contrast, the coal
ashes absorbed smaller amounts of NH3 (less than nominally 500 ppm), and most of the
absorption occurred in the first 5 to 10 minutes of exposure to the flue gas. For reference,
Figure 6 shows how the total ratio of NH3 to ash varied with exposure time during the course of
an experiment. If all of the NH3 were absorbed after one hour, the concentration in the ash
would have been 12,000 ppm for the 10 ppm NH3 case. This indicates that the coal ashes
absorbed nominally 2 to 6 % of the NH3, while the oil ashes absorb about 19 to 27% of the NH3.
The behavior of the Port Jefferson oil ash was qualitatively similar to that of the Oswego oil ash.
As shown in Figure 7, the amount of absorbed NH3 continued to increase linearly with time up
to a one hour exposure time, irrespective of temperature. However in contrast to the Oswego oil
ash, the slope of NH3 absorption for the Port Jefferson oil ash remained constant for exposure
times up to one hour. Also, there was no clear trend with temperature over the range for 250-
325°F.
The NH3 absorption characteristics of the coal ashes differed from the oil ashes in the following
aspects: (1) NH3 absorption was rapid for exposure times of 10 minutes and less, (2) the slope
of the NH3 absorption line stabilized after 10 minutes, and (3) temperature effects were evident.
The NH3 absorption characteristics of the Russel, Salem Harbor and Arapahoe coal ash are
discussed in the following paragraphs.
Figure 8 shows that the NH3 absorption on the Russel ash was initially very rapid, irrespective of
temperature. Above a temperature of 275°F, the NH3 absorption began to level off after
nominally 10 minutes, and only a slight temperature dependence was noted. Another
observation that was seen for all of the coal ashes was a change in slope of NH3 absorption
versus time. During the first 10 minutes, the absorption was fairly rapid; after 10 minutes, the
slope became more gradual. For the Russel coal ash, the slope was basically independent of
temperature. This change in slope with time suggests that the NH3 absorption may have
involved two different physical or chemical mechanisms. At long exposure times, the effect of
temperature is as expected; decreasing absorption with increasing temperature.
In Figure 9, the Salem Harbor ash's NH3 absorption also shows a temperature dependence in
addition to the exposure time dependence. As with the previous ash data, there appeared to be a
distinct change in slope with time. As expected, the lowest ammonia absorbances tended to
occur at the highest temperature of 325°F. During long term tests performed at Salem Harbor 3,
ash ammonia concentrations were measured over a two week period. The data showed that the
ash ammonia concentrations varied from 335 to 1554 ppm. Since these were grab samples, no
correlations with gas ammonia concentrations were possible. Subsequent tests were performed
at Salem Harbor, in which ash samples were gathered at the air heater exit. This sample location
provides a residence time of only a few seconds downstream of the urea injection location.
Analysis of these samples showed ash ammonia concentrations of nominally 2 ppm. These field
data support the residence time effects noted in the bench-scale tests. Exhaust gas ammonia
concentrations varied from 2 to 27 ppm during these tests, and showed no correlation with ash
-------
ammonia concentration. These results indicate that the majority of the ash ammonia absorption
occurs downstream of the air preheater; presumably on the ESP collection plates or in the ESP
hoppers.
Figure 10 shows the NH3 absorption characteristics of the ash from Public Service Company of
Colorado's Arapahoe Station. The NH3 absorption results from the Arapahoe ash showed the
same qualitative trends as the other coal ashes in terms of a distinct change in slope after 5-10
minutes. However, the temperature characteristics of this ash were quite different. While the
highest absorption occurred at the lowest temperature, NH3 absorption did not decrease with
increasing temperature. Above 300 °F, NH3 absorption increased for the 1-hour exposure. This
condition was repeated and the same trends observed. For reference, a full-scale sample was
obtained from the fabric filter hoppers while the SNCR system was operating on Arapahoe
Unit 4 under a 10 ppm NH3 slip limit. This sample had 285 ppm NH3 in the ash.4 (Note: the
fabric filter operates with an inlet temperature of nominally 250 to 290 °F.) This suggests that
the bench-scale 250 to 275°F data at residence times less than 20 minutes may be an indication
of full-scale behavior.
At a temperature of 275 °F, the Huntley ash was exposed to two different levels of NH3 slip, 10
and 20 ppm. The levels of NH3 absorbed by the Huntley ash were plotted as a function of
exposure time and NH3 slip level in Figure 11. These results show that the amount of NH3
absorbed after a given amount of time is also dependent on the NH3 slip level present in the flue
gas. When the amount of NH3 slip in the flue gas was doubled from 10 to 20 ppm, the amount
of absorbed NH3 increased by approximately 50% for exposure times greater than 10 minutes.
The NH3 absorption results discussed above are summarized in Table 3 for exposure times of 10
and 60 minutes.
Table 3
Summary: NH3 Absorption onto Fly Ash
(10ppmslipat300°F)
NH3 Absorption, wt ppm NH3 Absorption, wt ppm
Ash Type 10 Minutes 60 Minutes
Oil Ash:
Coal Ash:
Oswego
Port Jefferson
Huntley
Rochester
Salem Harbor
Arapahoe
432
467
95
159
166
222
1,893
1,654
132
190
344
347
-------
An attempt was made to correlate the NH3 absorption characteristic with the ash properties shown
in Table 2. In general, no correlation was found between NH3 absorption and either the carbon
content of the ash or the BET surface area. For the two oil ashes, the amount of NH3 absorbed
decreased with increasing ash pH. In contrast, the amount of NH3 absorption for the coal ashes
tended to increase with increasing pH as shown in Figure 12.
The only parameter that tended to suggest a correlation was the ash sulfate content, as shown in
Figure 13. The sulfate contents of the oil ashes where markedly higher than the coal ashes.
Correspondingly, the NH3 absorption was higher. However, within each type of ash, there was no
direct correlation between NH3 absorption and ash sulfate content.
Conclusions
During this exploratory study, a correlation between NH3 absorption and several different ash
characteristics was attempted. Although this study shed some light on the issue, no definitive
correlation was determined. Oil ashes were found to absorb substantially more NH3 than the coal
ashes. Additional research is needed in this area to help determine what factors govern NH3.
absorption onto differing types of ash. The work performed during this study suggested that the
amount of NH3 absorbed varies from ash to ash; this absorption does not appear to be governed by
BET, carbon, or pH levels. SO4 levels appeared to play a role, but the extent of this role was not
defined. Even the fairly alkaline coal ashes absorbed substantial amounts of NH3. The data showed
that the oil ash samples tested absorbed between 19 and 27 percent of the ammonia they were
exposed to, while the coal ash samples absorbed between 2 and 6 percent of the ammonia to which
they were exposed.
References
1. Muzio, L.J., Quartucy, G.C., State-of-the-Art Assessment of SNCR Technology, Electric Power
Research Institute, September 1993. TR-102414. [report]
2. Orion Model 95-12 Ammonia Electrode Instruction Manual, July 1990.
3. Quartucy, G.C., Personal Communication with Allen Sload, January 12, 1994.
4. Smith, R.A., et al., Integrated Dry NO/SO2 Emissions Controls System Baseline SNCR Test
Report, February 4-March 6, Department of Energy, 1992. DOE/PC/90550-T11. [report]
-------
100
V)
O
O
E
CO
3
M- O
O
-------
4000
3000 -
to
co
E
Q.
Q.
XT
O)
"CD
2000 -
1000 -
= 5 ppm
NH3 = 10ppm
NH3 = 20 ppm
NH3 = 50 ppm
20
40
60
80
100
Fraction Absorbed
Figure 2
Ash NH3 Concentration versus Fraction of NH3 Slip Absorbed
(10% Ash Coal)
-------
Vent / A
Gas Analysis
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Heat Traced
CO2 O2 N2 SO2 NH3
(From Compressed Gas Bottles)
FigureS
Bench Scale Ash Absorption Apparatus
-------
PH
Q Arapahoe
• Salem
A Huntley
° Rochester
• LILCO
• Oswego
0.0
3.0
Grams of Ash mixed in 200ml H2O
Figure 4
Ash pH Values
-------
Q.
Q.
"0
CO
I
3000
2500 -
2000 -
1500 -
1000 -
500 -
10
20 30 40
Exposure Time, minutes
(a) Exposure Temperature: 250 °F
A LILCO Oil Ash
x Oswego Oil Ash
A Huntley Coal Ash
o Rochester Coal Ash
• Arapahoe Coal Ash
n Salem Coal Ash
E
Q.
CL
+-»
D)
1
00
CO
<
3000
2500 -
2000 -
1500 -
1000 •
500 -
10
50
60
A LILCO Oil Ash
* Oswego Oil Ash
A Huntley Coal Ash
o Rochester Coal Ash
• Arapahoe Coal Ash
n Salem Coal Ash
20 30 40
Exposure Time, minutes
(b) Exposure Temperature: 300°F
FigureS
Ash NH3 Absorption as a Function of Exposure Time and Temperature
-------
E
Q.
Q.
3500
3000 h
2500 H
O) 2000 H
00
X
1500 H
1000 h
500 h
10
20 30 40 50
Exposure Time, minutes
60
A LILCO Oil Ash
* Oswego Oil Ash
A Huntley Coal Ash
o Rochester Coal Ash
• Arapahoe Coal Ash
n Salem Coal Ash
(c) Exposure Temperature: 325 °F
Figure 5
Ash NH3 Absorption as a Function of Exposure Time and Temperat
:ure
-------
E
Q.
Q.
•«—*
_D)
I
.g"
as
tr
CO
X
25000
20000
15000
10000
5000
0
NH3 = 20 ppm /
NH3= 10 ppm
0
10 20 30 40 50 60
Exposure Time, minutes
Figure 6
Relationship between Ash Exposure Time and NH3 to Ash Ratio
-------
E
Q.
Q.
O)
~O>
co"
X
10
20 30 40
Exposure Time, minutes
50
60
Figure?
Port Jefferson Oil Ash NH3 Absorption as a Function of
Exposure Time and Temperature
E
Q.
Q.
D)
00
I
250
200 -
150 -
100 -
10
20 30 40
Exposure Time, minutes
50
60
Figure 8
Rochester Coal Ash NH3 Absorption as a Function of
Exposure Time and Temperature
-------
I
Q.
oo
IE
10
20 30 40
Exposure Time, minutes
50
60
Figure 9
Salem Harbor Coal Ash NH3 Absorption as a Function of
Exposure Time and Temperature
£
Q.
Q.
0)
'
-------
350
NH3 Slip
E 10ppm
A 20 ppm
100
120
Exposure Time, minutes
Figure 11
Huntley Coal Ash NH3 Absorption as a Function of
Exposure Time and NH3 Concentration (T:275°F)
-------
500
400
E
Q.
Q.
D)
"
o
o
CO
JQ
CO
CO
<
300
200
100
0
Exposure
time
D 10 min
O 60 min
°0
7.0
8.0
9.0
10.0
11.0
Coal Ash pH
Figure 12
The Impact of Coal Ash pH on the NH3 Absorbed for a 10 ppm Flue Gas NH3
Slip Level and Variable Exposure Times at a Temperature of 300 °F
-------
500
Q.
~ 400
CD
O
CO
I
z
CO
300
I 200
100
0
0.0
0.2 0.4 0.6
Ash Sulfate Content, %
Exposure
Time
O 10 min
O 60 min
0.8
1.0
(a) Coal Ash
E
Q.
Q.
Il
D5
"CD
cf
o
o
CO
CO
X
CO
2000
1500
1000
500
0
D
O
T 1 « •—
Exposure
Time
10 min
60 min
B-
0
10 20 30
Ash Sulfate Content, %
40
(b) Gil Ash
Figure 13
The Impact of Ash Sulfate Content on the NH3 Absorbed by the Ashes for a
10 ppm Rue Gas NH3 Slip Level and Variable Exposure Times at a Temperature of 300°F
-------
PROBLEMS ENCOUNTERED DURING THE USE OF
AMMONIUM-CONTAMINATED FLY ASH
F.W. van der Brugghen
C.H. Cast
FCEMA
Utrechtsewg 310
6812 AR Arnhem
The Netherlands
J.W. van den Berg W.H. Kuiper
Dutch Fly Ash Corporation Maas power station
Utrechtseweg 370 N.V. EPZ
3731 GE De Bilt Roermondseweg 55
The Netherlands 6080 AA HAELEN
The Netherlands
R. Visser
VASIM
Winselingseweg 41
6541 AH Nijmegen
The Netherlands
Abstract
The most extensively used technology for flue gas treatment to reduce N0x-emission
is selective reduction with ammonia, either at 1000 °C in the gas phase (SNCR) or at
350 °C in the presence of a catalyst (SCR).
Operational problems that are encountered during application of these processes are
mainly caused by the slip of unreacted ammonia through the reaction zone or the
catalyst. This ammonia slip can lead to the formation and deposition of ammonium
salts in colder parts of the installation. In coal fired boilers contamination of the fly
ash with ammonium salts is possible, which can restrict re-use, especially because of
the ammonia smell during application.
Results will be described of laboratory tests with the preparation of mortars
containing fly ash with 100, 200 and 300 mg/kg ammonium. Ammonia
concentrations were continuously measured in ambient air during concrete mortar
preparation and the pouring of concrete floors. Furthermore, the compressive strength
and the ammonium content of the hardened concrete were followed.
Other tests were carried out at a production facility for sintered artificial gravel. Fly
ash with 300 mg/kg ammonium was used during these tests. Effects on working
conditions, product quality, ammonia emission and operational problems of the
installation were established and will be described.
Page -1 -
-------
Introduction
In several countries primary measures for N0x-emission reduction are currently
insufficient to achieve the increasingly tightened emission standards or emission
goals. It is inevitable that in such cases flue gas cleaning is applied. Two
technologies, both based on selective catalytic reduction of NOX with ammonia, have
reached maturity and are now widely applied:
. SNCR, selective non catalytic reduction or thermal DeNOx is based on a
homogeneous gas phase reaction between NOX and NH3 or urea at about 1000 °C
. SCR, selective catalytic reduction or catalytic DeNOx is based on a reaction
between NOX and NH3 at temperatures between 200 and 350 °C in the presence of
a catalyst.
The simplified overall reactions that take place with ammonia are:
4NH3 + 4NO + O2 -> 6H2O + 4N,
4NH3 + 2N02 + O2 -» 6H:O + 3N2
A very positive effect is that no large quantities of by-products that have to be
dumped are generated. N2 and H2O are constituents of the earth's atmosphere.
One of the operational problems of both technologies is caused by the slip of
ammonia through the reaction zone or the catalyst. This ammonia can react with
either SO2 or S03, compounds that are also present in the flue gas. The ammonium
sulphates that are formed can deposit on relatively cold surfaces, for instance in the
air preheater or in measuring lines. In coal-fired systems the fly ash can be
contaminated with those ammonium salts.
A large number of SCR systems is already in operation in coal-fired power stations
and ammonium contamination of the fly ash has indeed been observed. In well-
designed and properly operated systems the ammonium content of the fly ash can be
kept well below 50 mg/kg. It is generally assumed that this value does not influence
the applicability of the fly ash.
Page -2-
-------
However, with an increasing lifetime of the catalyst the activity decreases, which can
result in a higher ammonia slip and a higher ammonium content of the fly ash.
Furthermore a disturbance in the ammonia injection system can also lead to an
increased ammonia slip. It is therefore worthwhile to determine a kind of threshold
value for the ammonia content of fly ash, below which its application is not
hampered.
The work that will be described is aimed at three aspects:
. influence on the working conditions by the release of ammonia
. operational problems as a result of ammonia release
. the quality of products produced from ammonium contaminated fly ash.
Four applications of fly ash were studied:
. temporary storage (at a disposal site)
. production of concrete mortars (at the laboratory)
. pouring of concrete floors (at the laboratory)
. production of artificial sintered gravel (at a production facility).
Description of the tests and test results
Fly ash used during the tests
The fly ash used during the tests was produced at unit 6 of Maas power station in
Buggenum in the south-eastern part of the Netherlands. This unit has a net capacity
of 223 MW and is coal-fired.
A special SCR system was retrofitted in 1992 by replacing the two upper layers of
baskets from the two Rothemiihle combustion air preheaters by baskets with plate-
type catalyst material. Details of the demonstration programme performed with this
so called catalytic air preheater were presented at the previous NOX Symposium in
Miami Beach (1).
One of the results of this demonstration project was that the desired 30% NOX-
removal could only be reached with a high ammonia slip, resulting in ammonium
contents of the fly ash between 100 and 500 mg/kg. Analyses with the X-ray
photoelectron spectrometer (XPS) showed that the ammonia was present as
(NH4)2S04 at the surface of the fly ash particles.
Page -3-
-------
Temporary storage at a disposal site
At Maas-power station part of the ammonium contaminated fly ash had to be stored
temporarily at the fly ash storage site. To prevent dust formation, the fly ash leaving
the storage silos is moistened before being transported on a conveyor belt to the
storage site. At the end of the conveyor belt and at the disposal point an ammonia
smell was observed. The ammonia concentration in the ambient air was measured
with Drager test tubes and amounted to 20 ppm. No ammonia smell was observed
after completion of the work. Samples of the moistened fly ash taken at the end of
the conveyer belt had ammonium contents between 120 and 180 mg/kg.
Several days later, during the removal of the fly ash with shovels, an ammonia smell
was observed once again. No measurements were taken (2).
Preparation of concrete mortar
Concrete mortar with ammonium-contaminated fly ash, as a partial replacement of
cement, was prepared in a closed concrete mixer. The ammonia concentration of the
air in the mixer was measured continuously with a Laser Stark Spectrometer
developed by KEMA (3). The mortar has partly been cast in a closed vessel where
the ammonia concentration in the air was again measured continuously. The
remaining part of the mortar was used to produce standard cubes according to the
Dutch Standard NEN 5965. The compressive strength of these cubes was measured
according to NEN 5968 after hardening times of 7, 23 and 91 days. The presence of
ammonium was determined in the material of the tested cubes.
The concrete mixer used for the experiment could be closed with a lid containing
openings for sampling of the air from the mixer. Sixty litres of concrete mortar, of
the composition shown in table 1, was produced.
Table 1
Composition of concrete mortar
Portland cement A
fly ash
sand/gravel
water
ammonia content fly ash
3
230 kg/m
80 kg/m3
1770 kg/m3
196 kg/m3
300 mg/kg
Page -4-
-------
After filling the mixer with the ingredients, the lid was placed and mixing started.
Air was drawn from the mixer for the ammonia measurement. The results of the
ammonia measurements are shown in figure 1. The percentage of ammonium
originally present, that was released during the mixing, is also shown.
Within a minute after the start of the mixer the ammonia concentration in the air in
the mixer reached a value of 170 mg/m3. Stopping of the mixer resulted in a drop of
the ammonia concentration. At the end of the test, after 27 minutes, 10% of the
ammonia originally present had been released from the mortar.
Part of the mortar was cast in a closed vessel with openings in the lid for sampling
of the air from the vessel. Figure 2 shows the course of the ammonia concentration
in this closed vessel. There is a steady decrease in ammonia concentrated over time.
After 5 minutes the mortar was vibrated during 40 seconds. A small increase of the
ammonia concentration took place. After one hour 15% of the ammonium present
during pouring of the mortar had been removed from the closed vessel.
The cubes, that were cast with the remaining mortar were stored in a climatized
room at 20 °C and 95% relative humidity. Cubes prepared with ammonia free fly ash
were used as a reference.
After determination of the compressive strength of the cubes, the size of the
remaining material was further reduced to 1-3 mm with a jaw crusher. After steam
distillation of this crushed material, ammonium was determined
spectrophotometrically. The results are summarized in table 2.
Page -5-
-------
Table 2
Compressive strength and ammonia content of
concrete cubes made with ammonium-contaminated fly ash
ammonium-
contaminated
reference
hardening
time
days
7
7
28
28
91
91
7
28
91
compressive strength
N/mnr
18.6
18.3
23.8
29.6
40.3
40.8
24.8
34.7
47.2
% of reference
74.8
73.6
82.9
85.2
85.4
86.4
—
-
ammonium content
mg/kg
1.78
0.92
1.10
1.40
0.17
0.20
0.37
0.30
0.37
% of original
amount
13.9
8.9
10.7
13.6
1.7
1.9
—
—
-
After 28 days the compressive strength of the ammonium-containing cubes was 80%
of the reference value which is in the normal range.
After 7 days the ammonium-content of the material was 1 -2 mg/kg or 10-20% of the
original amount. After 91 days the ammonium-content was at the same level as in
the reference cubes (0.3-0.4 mg/kg).
Pouring of concrete floors
Three concrete floors have been made with mortars of the composition shown in
table 1. However, fly ash with three different""ammonium contents was used. One
floor was poured in an open room with natural circulation, the two other floors were
poured in a confined room. During all three experiments the ammonia concentration
in the room was measured continuously by means of the Laser Stark Spectrometer.
The floor in the open room with natural circulation was poured with mortar
containing fly ash with an ammonium content of 300 mg/kg. Only during pouring
could an ammonia concentration of 5-10 mg/m3 could be measured close to the
surface of the floor. Hardly any ammonia smell was observed.
Page -6-
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The two other floors were poured in a confined room. Fly ash with ammonium
contents of 100 and 200 mg/kg was used. During pouring of the floors an ammonia
smell was clearly observed. Figure 3 shows the ammonia concentration of the air in
the confined room as a function of the time elapsed after pouring.
In the case of fly ash with 100 mg/kg ammonium the concentration is already below
the olfactory detection limit at the start of the measurements. With 200 mg/kg
ammonium in the fly ash the initial concentration is 30 mg/m3 and steadily dropping.
Manufacture of artificial gravel
VASIM (Company for the manufacture of sintered products) in Nijmegen operates a
32 t/h plant for the production of sintered artificial gravel from fly ash. Figure 4
shows a simplified flow diagram of this plant.
Fly ash is transported to the plant by silo trucks and is stored in silos. Prior to
processing, air is blown through the fly ash in the silos to achieve homogenization.
The homogenized fly ash is fed to a mixer where pulverized coal and water are
added. The "mortar" thus formed is brought on a rotating pelletizing disc where the
so called "green pellets" are formed.
The "green pellets" drop from the pelletizer onto an open conveyor belt for
transportation to the sinter-installation. At the end of this conveyor belt the pellets
drop onto a short swinging conveyor belt, which spreads the green pellets on the
sintering bed. This sintering bed is built up on a moving grate and has a thickness of
about 0.3 m. The top of the bed is ignited with an oil-flame and the sintering is
supported by drawing air through the bed. The bed is divided into sections. Each
section has a duct for off-gasses. The temperature of the off-gas from the first
sections is around 100 °C, but with the downward progress of the sintering front in
the bed, the temperature rises to 400 °C in the further sections. Before being emitted,
the off-gases from all sections are dedusted" in a fabric filter installation. The
collected dust is recycled to the storage silos. The sintered product, Lytag, is cooled
and stored.
Ammonium contamination of the fly ash can cause several problems during the
Lytag production process:
. worsening of the working conditions through release of ammonia. This effect can
be expected in phases where moistened fly ash is in contact with ambient air:
pelletizer and conveyor belts
emission of ammonia into the atmosphere for instance with the homogenizing air
from the silos and the off-gas from the sinter installation
. operational problems.
Page -7-
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To establish the seriousness of the problems two one-day measuring campaigns were
carried out during which ammonium contaminated fly ash was processed. The
measuring programme during these campaigns is shown in table 3.
Table 3
Measuring programme during processing of
ammonium contaminated fly ash
homogenizing air from silos
homogenized fly ash
air near pelletizers
ventilation air pelletizers
air near transfer conveyor belts
green pellets pelletizer
green pellets transfer points conveyor belts
off-gas sinter plant before baghouse
off-gas sinter plant after baghouse
dust baghouse
campaign 1
wet chemical
wet chemical
Laser Stark
~
Laser Stark
wet chemical
wet chemical
wet chemical
wet chemical
wet chemical
campaign 2
—
—
Laser Stark
Laser Stark
DrSger tubes
wet chemical
wet chemical
wet chemical
wet chemical
wet chemical
Unfortunately, the measurements with the Laser Stark spectrometer failed during the
first campaign. The results of the second campaign are shown in figure 5.
Calibration of the device with a gas containing 100 ppm ammonia took place at
10 a.m., 12 a.m. and 3.15 p.m. The ammonia concentration in the air close to the
pelletizer shows a large number of peaks. Some of those peaks can easily be
explained. At 11 a.m. the pelletizer was stopped and 5 minutes later the value of
210 ppm was measured close to the pellets. The value of 270 ppm was measured at
the work place between the pelletizers after restart of the pelletizer. The peak at
12.15 h was due to the cleaning of the pipe through which the moistened fly-ash-
coal-mixture flows to the pelletizer. There is no "clear explanation of the other peaks.
The results of the other measurements are summarized in table 4.
Page -8-
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Table 4
Results of ammonia measurements during Lytag production
from ammonium contaminated fly ash
homogenized fly ash
homogenizing air
green pellets pelletizer
green pellets transfer point
ventilation air pelletizer
air near transfer point conveyor belts
off gas sinter plant before baghouse
emitted off-gas
dust collected in baghouse
Lytag pellets
campaign 1
304 mg/kg
< 0.5 mg/m3
324 mg/kg
315 mg/kg
-
~
50 mg/m3
5 mg/m3
13700 mg/kg
< 0.5 mg/kg
campaign 2
-
295 mg/kg
300 mg/kg
0.1-1.0 mg/m3
4-38 mg/m3
75 mg/m3
7-13 mg/m3
11600 mg/kg
-
There is no difference in the ammonium content of the green pellets on the pelletizer
and at the transfer point between the conveyor belts. A peculiar effect is that green
pellets on the pelletizer and on the conveyor belts sometimes smell and sometimes do
not smell of ammonia, although they all contain about the same amount of ammonia.
Near the transfer point between the two conveyor belts bursts of ammonia smell were
observed. During such short-lasting periods ammonia concentrations as high as
38 mg/m3 were measured with Drager rubes.
The ammonia concentration in the homogenizing air from the silo is negligible. The
off-gas from the sinter plant contains a very high ammonia concentration: 50-
75 mg/m3. Most of this ammonia is captured in the fabric-filter, but the emission
with the off-gas is not negligible (5-13 mg/m3). The dust in the baghouse has an
extremely high ammonium content. Values of above 10 g/kg (11.6 and 13.7 g/kg)
have been found.
Page -9-
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Discussion of the Results
Two general observations have been made:
- ammonia is only released from moistened fly ash or moistened mixtures
containing fly ash
- the release of ammonia from such moistened material to the atmosphere is
increased by any kind of mixing operation.
During the storage and removal of moistened fly ash from a disposal site, a
smell has only been observed close to the spot where activities took place. With
120-180 mg/kg ammonium in the fly ash, concentrations never reached the
MAC value of 25 ppm. During the storage period no ammonia could be
detected.
During the production of concrete mortar with fly ash containing 300 mg/kg
ammonium in a closed mixer, extremely high ammonia concentrations far above
the MAC value were reached. However, due to rapid mixing with ambient air
the concentration around an open mixer rapidly dropped below the olfactory
detection limit.
Casting a concrete floor containing fly ash with 300 mg/m 3 ammonium in a
relatively large well ventilated room did not reveal any smell problems.
However, in confined spaces ammonia concentrations above the MAC-value
were found with fly ash containing 200 mg/kg ammonium. Only slight smell
problems during a short period after casting were experienced with 100 mg/mg
ammonium in the fly ash.
During manufacturing of sintered artificial gravel ammonia concentrations
exceeding the MAC value have been observed occasionally near the pelletizers,
the only workplace occupied 24 hours a day. Disturbances in the pelletizer
operation even lead to short-lasting, unacceptably high concentrations. The
MAC value has also been exceeded occasionally at the transfer point between
the two conveyor belts.
The very high concentration of ammonia in the off-gas from the sinterplant can
possibly lead to an increase of the pressure difference across the fabric-filter.
However, the duration of the campaigns (20 h) was too short to enable
establishment of such effects.
The very high ammonium content of the dust collected in the baghouse and
recycled to the storage silo can in principle lead to an increase of the ammonia
content of the fly ash processed in the plant, even if the quality of the delivered
flv ash is constant.
Page -10-
-------
Ground-level concentrations of ammonia in the surroundings due to storage
operations, mortar production and concrete casting will not be disturbing to the
general public. Ammonia emission with the off-gas from the sinter plant could
probably increase when contaminated fly ash is processed during a longer
period. The campaigns were relatively short and the greater part of the ammonia
present in the off-gas could still be absorbed on the acid surfaces of the ducts
and filter bags that existed prior to the start of a campaign. During campaign 2
there was a slight indication of an increase in emission over time.
Ammonia did not negatively influence the quality of concrete test cubes and
Lytag pellets.
Conclusions
The following conclusions can be drawn from the described experiments with
use of ammonium contaminated fly ash:
. No problems need to be expected during handling of dry fly ash contaminated
with ammonium
. Moistening of ammonium contaminated fly ash or mixtures containing such
fly ash can lead to the release of ammonia. The release rate of ammonia
from such mixtures is increased by any mixing operation
. No general threshold value can be formulated for the ammonium content of
fly ash to prevent any influence on working conditions and operational
problems. This threshold value is process-specific.
. Hardly any or no smell nuisance need to be expected during disposal
operations or during use of fly ash containing 100 mg/kg ammonium or less.
. Some smell nuisance may be expected at 200 mg/kg ammonium.
. Surpassing of the MAC value of 18 mg/m 3 is possible at 300 mg/kg
ammonium (casting of mortar in confined rooms, artificial gravel production).
. No influence of ammonium contamination of fly ash on product quality has
been found.
. Operational problems can be expected during artificial gravel production due
to the high concentration of ammonia in the off-gas downstream of the sinter
plant. A greater pressure drop across the fabric filter for dust removal is not
unlikely. During prolonged use of ammonium containing fly ash the ammonia
content of the fly ash processed in the plant will increase as a result of the
recycling of heavily contaminated dust from the fabric filter.
Page -11-
-------
Acknowledgements
The work described in the paper has been funded by the Dutch Fly Ash
Corporation and by the Dutch Power production companies in their Collective
Research and Development Contract.
We thank Roy Verhoef and the staff of KEMA's laboratory for by-products and
construction quality in performing the "concrete work" and Leo Wouters, Rudy
Rooth and Ad Verhagen for the performance of ammonia measurements with
the Laser-Stark Spectrometer.
Page -12-
-------
References
1 Hiittenhofer, K., Beer, J., Smeets, H., Van der Kooy, J. The DeNOx Air
preheater downstream of a coal fired boiler.
EPRI/EPA 1993 Joint Symposium on Stationary Combustion N0x-control.
Miami 24-27 May, 1993.
2 Van der Brugghen, F.W., Van Dijseldonk, A.C.W.M., Imandt, J.J.C, Essers,
J.C.M., Kuijper, W.H.
The demonstration programme Catalytic Air-preheater at Unit 6 of Maas power
station.
KEMA 14566-KET/STF 93-6002 (May 1993) (In Dutch).
2 Verhagen, A.J.L., Rooth, R.A., Wouters, L.W. Laser Stark Spectrometer for the
measurement of ammonia in flue gas.
Applied Optics 32 (no. 30) 5856-5866 (1993)
Page -13-
-------
-------
I
0)
en
en
-------
o
o
-------
fly-ash
silo
_J t_
coal
silo
}
We
ter
homonanizinn air
pelletizer
conveyor belts
sinterplant
oil
burner
D rr
off-gas
baghouse
-to stack
T
dust
(to fly-ash silo)
Figure 4
Scheme of LYTAG-production facility
Page -17-
-------
-g 3OO
ja
^ 250
0)
N
I 200
150
Q)
U
m
100
50
O
1O 11 12 13 14
time of the day- • [hours]
15
16
Figure 5
Ammonia concentration in the air near a pelletizer
of the Lytag production facility
Page -18-
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Session 8B
Rebuming
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DEVELOPMENT AND INDUSTRIAL APPLICATION OF OIL-REBURNING
FOR NOX EMISSION CONTROL IN UTILITY BOILERS
G. De Michele
S. Pasini
ENEL-DSR/CRT - Via Andrea Pisano, 120 Pisa (Italy)
R. Tarli
S. Bertacchi
ENEL-DPT/STE - Via Andrea Pisano, 120 Pisa (Italy)
R. De Santis
G. Mainini
ANSALDO ENERGIA Piazza Monumento,12 Legnano (Italy)
T. Dorazio
ABB/CE Services, 200 Great Pond Drive, Windsor, Connecticut(U.S.A.)
G. Mascalzi
ABB/ITCRC - Piazzale Lodi, 3 Milano (Italy)
Abstract
ENEL is conducting a comprehensive modification program within its generating system, in order
to comply with the new Italian air quality standards for fossil fuel-fired power plants, which set a
limit for NOX of 200 mg/Nm3 corrected to 3% 02 for oil and gas and to 6% C"2 for coal.
Among all combustion modification technologies reburning has proven particularly attractive,
since it has been demonstrated that it generally permits to satisfy the regulatory requirements in
gas and oil fired units, thus avoiding the use of SCR.
The ENEL generating system essentially employs tangentially fired (TF) and front/opposed wall
fired boilers belonging, respectively, to the CEI and Babcock & Wilcox (B&W) technology,
designed and constructed by Ansaldo and Franco Tosi (now bought by Ansaldo). In this
framework ENEL has signed respectively with Ansaldo Energia and Combustion Engineering Inc.
(CEI), and with Ansaldo Energia two separate agreements to apply Reburn Technology in oil and
gas, tangentially-fired (TF) utility boilers, the first, and oil and gas wall-fired (WF) utility boilers,
the second, both in Italy and abroad.
This paper outlines the technical knowledge available for the design of reburn systems for a
retrofit application and describes the main results obtained, after retrofit, at Torvaldaliga #2
power station, 320 MWe (TF), firing both oil and gas as reburn fuels, and at Cassano unit #1, 75
MWe (WF), firing gas as main and reburn fuels.
Reference is also made to the development of the projects for the application of the technology at
Monfalcone, 320 MWe (WF), in the oil over oil configuration, whose demonstration is planned
-------
for the Autumn of 1995, and at Porto Tolle unit #1, 660 MWe (TF), that is planned to start in
January 1996.
Introduction
ENEL is conducting a comprehensive modification program within its generating system, in order
to comply with the new Italian air quality standards for fossil fuel-fired power plants, which set a
limit for NOX of 200 mg/Nm3 corrected to 3% QI for oil and gas and to 6% Oi for coal *'2
Both in furnace and post combustion technologies are applied. For coal fired units high-dust SCR
can typically be installed, but on going projects will try to demonstrate more cost-effective
options which involve in-furnace NOX reduction techniques plus smaller (in-duct) SCR.
For oil and gas fired units the goal is to obtain the highest possible reduction of NOX through
combustion modifications (Burners Out of Service (BOOS), use of low NOX burners, separated
overfire ports, gas mixing, etc..) and, only after that, considering the use of SCR, if necessary.
Among all combustion modification technologies reburning has proven particularly attractive,
since it has been demonstrated that it generally permits to satisfy the regulatory requirements in
gas-oil combustion, thus avoiding the use of SCR3
The ENEL generating system essentially employs tangentially fired (TF) and front/opposed wall
fired boilers belonging, respectively, to the CEI and Babcock & Wilcox (B&W) technology,
designed and constructed by Ansaldo and Franco Tosi (now bought by Ansaldo). For both
configurations the technology has evolved from bench to full scale units and is now supported by
demonstration projects for rated powers up to 660 MWe, some in operation and some in
implementation *£
In Italy, after the first full scale application carried out by ENEL and Ansaldo, ENEL is co-
operating with Ansaldo, a major Italian manufacturer, and, for TF boilers, also with CEI, with the
aim of taking advantage of the collective experience of all the parties (ENEL, ANSALDO and
CEI) in order to provide utilities with proven technology, which is reliable and cost effective.
This paper is focused on technology development and experience on tangentially and front and
opposed wall fired boilers.
Technology Background
More than 30 years ago Myerson 6 discovered that hydrocarbon radicals quickly react with NO
leading to the formation of N2 and H20 and Wendt, 15 years later, named the technique that
exploits this reaction for reducing NOX "Reburning" 7.
When part of the fuel and combustion air are added separately to the post flame region instead of
to the main combustion zone, a three stage combustion process is obtained. The first stage, where
about 85% to 90% of the heat is released, is normally run with nearly stoichiometric excess air.
The reburning fuel, which usually constitutes 10% to 15% of the total fuel, is injected after the
primary combustion zone to form a fuel-rich second stage, where NO is reduced. Downstream of
the reburning zone, post combustion air is added to secure complete burnout.
ENEL, since 1988, have started what is called the "Reburning Project", consisting in the
development of a technology capable of reducing NOX emissions below 200 mg/Nm3 (98 ppm) in
oil fired power stations, acting only on the combustion system of the plants 8
-------
To reach the above goal laboratory experiments have been carried out at different scale and
mathematical models have been developed to improve the system and transferring the technology
to full size plants.
At the beginning attention has been focused on tangentially fired boilers utilising, in sequence, a
50 kWt furnace (ENEL Livorno Labs), a 25 MWt boiler simulator (CEI Windsor) and a 35 MWe
boiler (ENEL Santa Gilla power plant) 9. Successively an industrial application has been carried
out by ENEL and Ansaldo at Fusina (160 MWe). The retrofit of a 320 MWe unit has been
recently completed (Torrevaldaliga 2) and a retrofit on a 660 MWe unit (Porto Tolle #1) is now in
the final design stage, by ENEL, Ansaldo and CEI.
Based on the completely satisfactory results gained, ENEL and Ansaldo decided to apply the
same concepts and the same methodology to wall fired boilers going through laboratory studies,
tests on a 6 MWt boiler simulation facility (Ansaldo CCA Gioia del Colle) and design and
industrial application on a 75 MWe front fired unit (AEM Cassano D'Adda). Using the numerical
tools developed and the industrial experience already gained on TF boilers a retrofit has been
designed on a 320 MWe opposed fired unit (Monfalcone 3) which will be operational by Autumn
1995.
Common characteristic for all these applications is the use of the reburning technology in the "oil
over oil" configuration (oil main fuel/oil reburn fuel) and the reaching of NOX emission values
below 200 mg/Nm3 without any negative impact on boiler performance, CO and particulate
emission.
Tangentially-Fired Boilers
Based on the outstanding results obtained in the Fusina #5 retrofit, ENEL has launched the
program for application of oil reburning on many of its generating units. As tangentially fired
boilers are concerned, two retrofits are in progress, one related to a 320 MWe unit
(Torrevaldaliga #2) of which the first results are available, the other related to a 660 MWe unit
(Porto Tolle #1).
Torrevaldaliga #2 Retrofit
The Torrevaldaliga #2 boiler (320 MWe) has been retrofitted to oil-reburning. The boiler was
equipped with 20 burners located at five elevations. The pre-retrofit configuration of the
combustion system already included an overfire air system (close coupled and separated air
nozzles) located in the furnace corners and a gas mixing system (flue gas recirculation to the
windbox). An extensive study of process parameters, made with large use of numerical
simulations, led to a "close coupled" reburn arrangement, to maximise the distance between the
reburn fuel and post combustion air injectors, and to take benefit from the near burner high
temperature field, with a global repositioning of the post combustion air nozzles with their vertical
displacement the boiler walls.
The "close coupled" reburn arrangement has involved the reduction from 5 to 4 of the main
burner elevations. The optimisation process of mixing between the main stream and the additional
jets was carried out through extensive 3-D mathematical modelling which led to the final solution
(Fig. 1):
4 reburn nozzles located on the corners using high-speed injectors;
-------
6 post combustion air ports located on both front and side walls, equipped with high speed
injectors and different yaw angles.
Plant conversion was completed on October '95 and first testing is now conclused.
Three main configurations were analysed: baseline, staged combustion and reburning, with both
oil and gas as reburning fuels. With reference to baseline NOX emissions of 750 mg/Nm3, a
reduction efficiency of about 80% was obtained at full load, with lowest NOX emissions of 150-
160 mg/Nm3 both for oil and gas reburning. These values were obtained with final O2 of 2%, only
slightly greater than baseline value. Thermal performance was very good , and it was possible to
keep SH and RH steam temperatures at their design value of 540°C. Quite surprising was the
small difference, in terms of NOX emissions, between oil and gas reburning. This is probably due
to the good mixing realised in the furnace and to the high residence time in the reburn zone (of the
order of 0.5 s).
Good results were obtained also with staging (final NOX of about 200 mg/Nm3), but at a much
higher final O2 (2.5 to 3%) and without maintaining final steam temperatures to their design
value.
In Fig. 2 NOX emissions are shown for the different configurations of the combustion system
examined: in the case of oil-reburning the optimum reburn oil fraction is of 10%, that corresponds
to a reburn zone stoichiometry of 0.87. Figure 3 shows the effect of the quantity of recirculated
flue gas on opacity and NOX emissions in the oil reburning configuration. It appears that the
process can work correctly also lowering FOR flow rate down to 6%, from the design value of
15%: this is probably due again to the high residence time in the reburn zone, that favours mixing.
Oil reburning has proven to be very effective also at low load, as shown in Fig. 4: it is always
possible to maintain NOX emissions well below the legislation limit of 200 mg/Nm3 from full load
(300 MWe) down to control load (150 MWe).
Testing is now proceeding with a detailed in-furnace mapping of temperatures and chemical
species, for a better understanding of the reburning process.
Porto Tolle #1 Retrofit
The unit is a tangentially fired, oil fuelled, supercritical boiler, rated 660 MWe, originally equipped
with 24 burners located at 6 elevations. The boiler in its previous history has experienced severe
problems of furnace wall overheating. As a consequence the application of reburning technology
has required careful investigation, because any change in the combustion system affects thermal
flux to the waterwalls and waterwall heat absorption. A complete pre-retrofit characterisation has
been performed focusing on the most critical parameters (burners elevations; hopper flue gas
recirculation, air biasing on the windbox compartments, etc.) and examining local heat fluxes on
the waterwall. The subsequent process design activity has led to the selection of a "close coupled"
reburn arrangement reducing to 5 the number of burner elevations (from 6 originally). The 3-D
numerical modelling activity, for mixing optimisation, was completed, providing optimal location,
sizing and orientation of reburn and post combustion air nozzles. All nozzles are intended to
provide high momentum jets to assure fast mixing; due to furnace cross section (16.4*13.7 m)
two reburn injectors located in the centre of the front and rear wall were added to the standard
four injectors in the corners. The conversion of the unit will start in September this year an testing
is forecast to start January 1996.
-------
Front/Opposed Wall-Fired Boilers
The first reburn retrofit on a front fired boiler (AEM Cassano D'Adda, 75 MWe) has been recently
completed by Ansaldo. In parallel to the development of the design of retrofit of Torrevaldaliga 2,
ENEL has also launched with Ansaldo the design of the reburn retrofit of Monfalcone #3, a 320
MWe, oil fuelled, once-through, B&W design, opposed wall-fired boiler. The boiler will return to
service on July 1995. This retrofit will be the demonstration unit for other retrofits of similar
units, the firsts of which will be the four units of La Casella.
Cassano D'Adda - AEM Retrofit
This boiler gas/oil fuelled, natural circulation was originally equipped with 9 burners of the
circular type located in three rows. The retrofit project was very extensive with a complete
redesign of the combustion system with the following main features (Fig. 5):
use of 6 three-flow low NOX burners of the TEA type 10 located in two rows for oil and gas
firing;
use of three reburn injectors located in a single row in the front wall;
use of three post combustion air injectors located in a single row in the front wall.
Both reburn and post-combustion injectors are of the circular type with axial primary flow and
swirled secondary flow. A gas recirculation system provides flue gas flow to the hopper for
temperature control, to the combustion air for gas mixing and NOX control at the burners, and to
reburn injectors for jet mixing.
A baseline assessment of the boiler was made prior to modifications. The boiler has now returned
to service and a program of characterisation was completed. Collected data for gas firing,
summarised in Fig. 6, show the following NOX values, in respect of a baseline in the range of 550
-r- 600 mg/Nm3
low NOX TEA burners only NOX ~ 220 mg/Nirp;
gas over gas reburning : NOX ~ 160 mg/Nm3
gas reburning + gas mixing : NOX ~ 80 mg/Nm3;
Monfalcone 3 Retrofit
Lay-out and engineering studies have been recently completed in order to retrofit Monfalcone unit
3 with an oil reburning system. The problem of retrofitting Monfalcone proved difficult due to
numerous mechanical constraints. The design and the data obtained via 3-D computer modelling
have been validated also via physical modelling (cold flow tests) and via tests on the Ansaldo
Boiler Simulation Facility. The combustion system configuration will include four reburn injectors
both on front and rear walls and six overfire air ports, three on each side wall (Fig. 7).
At present the boiler is equipped with 18 low NOX TEA burners which will remain in service and
will be used as main burners. In the start-up phase it will be decided whether to use 12 or 18
burners. The reburning injectors are designed for high speed injection and tilt/yaw adjustment
using flue gas as transport medium.
The Monfalcone retrofit is a good example of how a reburning retrofit design depends on boiler
type and site boundary conditions.
-------
Conclusions
On the basis of the extensive knowledge existing to-day and the results of the recent
demonstration conducted at Torvaldaliga (320 MWe, TF), it is possible to confirm that oil over oil
reburning allowes to obtain as much as 80% abatement of NOX and to reach emissions well below
the regulatory requirement in Italy (200 mg/Nm3) in both tangentially and front/opposed wall-
fired boilers.
ENEL is waiting for the experimental results of the two planned demonstrations at Monfalcone
(320 MWe, WF), and Porto Tolle (660 MWe, TF), and if there will be a confirm of the results
obtained up to now, oil-oil reburning will be applied in most of ENEL generating units as an
alternative to the use of SCR's, providing environmental benefit in a short time frame and at
competitive cost.
ENEL S.p.A., Ansaldo Energia, and Combustion Engineering Inc. (CEI) have collectively
developed a deep knowledge and experience in the application of reburning to oil-gas fired utility
boilers and they are capable of providing utilities with proven technology, which is reliable and
cost effective.
Acknowledgements
The authors would like to thank the ENEL Department of Production and Transmission of
Civitavecchia and Torvaldaliga Power Station for their assistance during the trial period.
References
1. A. Benanti, G. De Michele, R. Tarli and G. Bianchi; "Retrofitting of the Italian Electricity
Board's Thermal Power Boilers", Proceedings of the Symposium on NOX Control for Utility
Boilers, Cambridge, MA (July 1992).
2. A. Benanti, S. Bertacchi, G. De Michele, M. Livraghi, S. Pasini, and R. Tarli, "Primary
Technologies for NOX Reduction in ENEL (Italian Electricity Company) Fossil-Fired
Boilers", Proceedings of the UNIPEDE/IEA Conference, Thermal Power Generation and
the Environment, Hamburg, Germany (September 1993).
3. G. De Michele, S. Pasini. S. Bertacchi, R. Tarli, A. Benanti, M. Livraghi, G. Mainini, R. De
Santis; "Field Evaluation of Oil-Reburning for NOX Emission Control in a 160 MWe
Tangentially Oil-Fired Boiler", EPRI/EPA Symposium on Stationary Combustion NOX
Control, Miami Beach, (May 1993).
4. S. Pasini, G. De Michele, A.Benanti, R.Tarli, R. De Santis;"Development and Industrial
Application of Oil Reburning for NOX Emission Control", Power Gen Europe '94, Cologne,
(May 1994).
5. G. De Michele, S. Pasini, R. Tarli, G. Girardi, R. La Flesh, S. Caruso, R. De Santis ; " Oil-
Reburning, a viable way to meet the Regulatory Requirements for NOX control in oil-gas
fired utility boilers ", International Joint Power Generation Conference Phoenix (October
1994).
-------
6. A.L. Myerson, F.R. Taylor, and E.G. Faunce. "Ignition Limits and Products of the
Multistage Flames of Propane-Nitrogen Dioxide Mixtures" Sixth Symposium (Int.) on
Combustion, 154, The Combustion Institute (1957).
7. J.O.L. Wendt, C.V. Sterling, and M.A. Matovich. "Reduction of Sulfur Trioxide and
Nitrogen Oxides by Secondary Fuel Injection" Fourteenth Symposium (Int.) on
Combustion, p. 897, The Combustion Institute (1973).
8. L. Baldacci, S. Bertacchi, G. De Michele, S. Pasini; "Reduction of NOX Emissions by Gas
Reburning Technology", Joint Meetings of the Flame Aerodynamics, Chemistry of Flames
and Heat Transfer, IFRF, Roskilde, Denmark, (October 1988).
9. R.C. La Flesh, J.L. Marion, D.P. Towle, C.A. Maney, G. De Michele, S. Pasini, S.
Bertacchi, A. Piantanida, G. Galli, G. Mainini; "Application of Reburning Technologies for
NOX Emissions Control on Oil and Pulverised Coal Tangentially-Fired Boilers", Proceedings
of the Int. Joint Power Generation Conference, San Diego, (October 1991).
10. G. De Michele, G. Benelli, S. Ligasacchi, A. Benanti, R. Tarli, M. Alberti, and R. De Santis;
"Development and Industrial Application of an Oil and Gas Low NOX Burner", EPRI/EPA
Symposium on Stationary Combustion NOX Control, Miami Beach, (May 1993).
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O
£DU ~
200 -
150 -
100 -
50 -
0 -
P,
_ S| m NDx
\ ^.
\ Q-— ^
OPACITY ^
i i
- 20
- 15
- 10
- 5
- 0
0% 5% 10%
S?
X
K-
M
CJ
t
Q.
O
FLUE GAS RECIRCULATED, (%)
Fig.3 - TORVALDALIGA UNIT #2 - EFFECT OF FGR FLOW
RATE ON NOx EMISSIONS, WITH OIL REBURN ING.
-------
400
350 -
| 300 -
0)
6 250 -
^ 200
£2 150 -
O 100 -
50 -
0
50
OIL-REBURN
100
150
200
250
300
350
UNIT LOAD, (MWe)
Fig.4 - TORVALDALIGA UNIT #2. NOx EMISSIONS VERSUS
LOAD FOR BASELINE AND REBURN CONFIGURATIONS
Fig. 5 - AEM CASSANO UNIT #j - NEW GAS REBURNING SYSTEM
-------
8
600
500-
400 -
300 -
POO -
100 -
LNB = LOW NOx BURNERS
GR = GAS REBURN
GM = FLUE GAS MIXING
CIRCULAR BURNER
LNB + GR
LNB + GR + GM
0
0.85 0.90 0.35 1.00 1.05 1.10 1.15 1.20
REBURN ZONE STOICHIOMETRY. SR2 (-)
Fig.6 - AEM CASSANO UNIT #1 - NOx EMISSIONS
WITH GAS AS MAIN FUEL.
OFA
REB
LOW NOx
BURNERS
OFA
REAR HALL
REBURN
1
-
—
t
1 1 ,
t
-
t T
REBURN
FRONT W4LL
OFA
Fig. 7 - MONFALCONE UNIT #3.
FINAL REBURN SYSTEM ARRANGEMENT
-------
-
m
^ 480-
cn
lo(J
fr) 440-
X
0
Id(J
UNIT
COMBUST
CONFIG
BASELINE
NOx
mg/Nm
(55%) ^ _^
(
64%
CO
-=3;
CD
;
— j
Q
S GILLA #2
35 MWe
TANGENT
440
(
1
ACTUAL LEGISLATION LIMIT
* J_ _L
77%)
I-H
Q
(79%)
(80%) (80%)
~J
t-H
0
h- ^ ^ (priv)
~~r- rr~. r~-. [IJUAjj
CD
1— 1
CD
FUSINA 5 TOFIVALDALIGA 2 CASSANO
160 MWe 320 MlVe 75 M(Ve
TANGENT TANGENT FRONTAL
(*)
750 750 600
(*) MAIN FUEL IS GAS
(NOx REDUCTION EFFICIENCY)
Fig.8 - SUMMARY OF THE RESULTS OBTAINED WITH THE
REBURNING TECNOLOGY IN OIL AND GAS,
TANGENTIALLY AND WALL-FIRED BOILERS.
-------
Advanced Reburning With New Process Enhancements
Blair Folsom, Roy Payne, David Moyeda, and Vladimir Zamansky
Energy and Environmental Research Corporation (EER)
18 Mason
Irvine, California 92718
Jerry Golden
Tennessee Valley Authority
1101 Market Street
Chattanooga, Tennessee 37402
Abstract
Advanced Reburning (AR) is a synergistic integration of reburning and selective non-catalytic
reduction (SNCR) which can reduce NOX emissions by over 85% from boilers and furnaces.
Reburning is used to set up conditions which optimize the performance of SNCR including
broadening of the temperature window and reduction of ammonia slip. AR has been tested
extensively at pilot scale as part of two DOE projects. Recently, two AR improvements have
been developed and tested at bench scale: reagent injection into the reburning zone and
specific promoters which enhance NOX control, broaden the SNCR temperature window, and
further reduce ammonia slip. The reburning zone reagent injection can be used to eliminate
the injection of urea or ammonia SNCR agents thus significantly reducing total capital cost.
Alternately, two injection stages can be used to increase NOX control to 95%. This paper
presents the results of pilot and bench scale tests of both the AR and the new process
enhancements. Plans for additional development and a full scale field evaluation are
discussed.
Introduction
Title 1 of the Clean Air Act Amendment (CAAA) of 1990 requires NOX controls in ozone
non-attainment areas. The initial Title 1 regulations, implemented over the last few years,
required Reasonably Available Control Technologies (RACT). In most areas, the NOX levels
for RACT are now in the range of 0.4 to 0.5 lb/106 Btu which can generally be achieved
using low NOX burners (LNB). As a result, there has been little industry demand for higher
efficiency and more expensive NOX controls such as reburning, SNCR, and SCR. However,
the current RACT requirements are not the end of NOX regulations. Additional more stringent
NOX control may be required to bring many of the ozone non-attainment areas into
compliance, particularly in the Northeast. Post-RACT regulations are now being drafted to
implement deeper NO, control and to require offsets for new sources. The NOX control
requirements are being based to a large extent on Selective Catalytic Reduction (SCR), the
commercial technology with the highest NOX control efficiency.
-------
This paper discusses Advanced Reburning (AR), a synergistic integration of reburning and
Selective Non-Catalytic Reduction (SNCR) which offers the potential to achieve the NOX
control of SCR but at significant cost savings. AR was initially developed by Energy and
Environmental Research Corporation (EER) as part of a DOE reburning optimization
project.1-2 Rather than simply applying the two technologies simultaneously, AR uses the
reburning process to optimize conditions for SNCR. This broadens the SNCR temperature
window and improves utilization of the injected ammonia or urea. AR has been tested over a
range of scales up to 10 x 10s Btu/hr and achieved NOX control in the range of 85%.
Recently, EER has identified two enhancements to AR:
• Specific Promoters EER has identified additives which considerably enhance the NOX
control from ammonia or urea injection in the AR process. These "promoters" are
common water soluble inorganic salts which can be added to aqueous ammonia or urea.
• Agent Injection into the Reburning Zone Recent tests at EER have shown that a specific
agent can also be injected into the reburning zone. This allows two stages of injection
for deeper NOX control.
By integrating these improvements with AR, NOX control can be increased to over 95% for
cyclone units and even higher for pulverized coal fired units (wall and tangentially fired)
where AR can be further integrated with low NOX burners and overfire air. These second
generation AR systems are intended for post-RACT applications in ozone non-attainment
areas where NOX control in excess of 80% is required. The total cost of NOX control for
second generation AR systems is on the order of half of that of SCR. Also, the catalyst, duct
modifications, and catalyst disposal problems of SCR are eliminated.
This paper presents the technical basis of AR and the new AR process enhancements. AR
was tested at up to 10 x 106 Btu/hr and the process enhancements were tested at 1.0 x 106
Btu/hr. Various embodiments of the AR system can be configured to achieve NOx control
comparable to SCR. The tradeoffs among these configurations are discussed. Finally, plans
for additional development and a full scale demonstration are presented.
Technical Basis
Advanced Reburning
AR is the integration of reburning and SNCR. This section presents an overview of these two
components and then discusses their synergistic integration.
Reburning. Reburning, a fuel staging method for NOX control, was suggested by Wendt et
al.3 With reburning, the combustion process is divided into three zones as illustrated in
Figure 1. In the primary zone, the main fuel (which can be coal, oil or gas) is fired through
conventional burners but at a reduced rate to compensate for the reburning fuel which is
injected downstream.
-------
The reburning fuel is injected into the combustion products from the first stage. A portion of
the fuel consumes the available oxygen and the remainder provides a fuel-rich mixture with
carbon radicals: CH3, CH2, CH, C, HCCO, etc. These active species can participate either in
formation of NO precursors in reactions with molecular nitrogen or in reactions with NO.
Many elementary steps can share responsibility for NO reduction, and there is no commonly
accepted opinion about their importance. Miller and Bowman4 suggest that the main reaction
paths converting NO to N2 include NO reactions with C and CH: C + NO - CN + O, CH
+ NO - HCN + O and CN and HCN are oxidized to NCO. The carbon containing radicals
(CHj) formed hi the reburning zone are capable of reducing NO concentrations by converting
it to various intermediate species with C-N bonds. These species are reduced in reactions
with different radicals into NHj species (NH2, NH, and N) which react with NO to form
molecular nitrogen. Thus, there are two types of chemical reactions of NO removal: with CH;
and with NH; radicals.
Overfire air is added in the final burnout zone to complete the combustion and to adjust the
overall excess air. Thus, except for relatively minor changes in boiler efficiency, the total
heat input to the furnace is the same as baseline but divided into two streams. Similarly, the
total air supplied to the furnace remains essentially unchanged but is divided into two streams
which supply the conventional burners and the overfire air ports.
Reburning can be applied using any hydrocarbon fuel. On a purely performance basis,
natural gas is the ideal reburning fuel for a number of reasons. However, it is generally more
costly than coal on a heating value basis ($/106 Btu). Reburning has been demonstrated on
several full scale boilers and is offered commercially by several vendors including HER.5'12
Selective Non-Catalytic Reduction (SNCR). SNCR controls NOX by reaction with
ammonia or urea injected into the high temperature combustion products. The corresponding
commercial SNCR methods are the Thermal DeNOx and NOXOUT processes. The Thermal
DeNOx process was invented by Lyon13 and described hi detail by Lyon and Hardy.14 When
ammonia is injected into combustion flue gas containing NO and oxygen at temperatures
between 1500 and 2000°F, a chemical reaction occurs and NO is converted to molecular
nitrogen. The reaction starts with formation of Nf^ radicals: NH3 + OH - NH2 + H2O
which can be also formed in reactions with O and H atoms: NH3 + O - NH2 + OH and
NH3 + H -* NH2 + H2. The main elementary reaction of NO to N2 conversion is: NH, + NO
- N2 + H2O.
Urea, (NH2)2CO, was suggested by Arand et al.15 and is used hi the NOXOUT process. The
mechanism of urea injection includes the important features of the NHj and HNCO reactions
with NO, because urea is rapidly converted to NH3 and HNCO at high temperatures:
(NH2),CO - NH3 + HNCO. The most important HNCO reactions with radicals are: HNCO +
H - NH2 + CO and HNCO + OH - NCO + H2O. As hi the Thermal DeNOx process, NH2
radicals can either remove NO: NH2 + NO - N2 + H2O or form NO via HNO radicals. NCO
radicals can remove NO to form N2O: NCO + NO -* N2O + CO. The N2O and CO may exit
as byproduct pollutant or may be oxidized by OH and H: CO+OH-*CO2+H and
N2O+H-N2+OH.
-------
One of the key practical problems with SNCR is that it is quite sensitive to temperature.
Optimum NOX reduction occurs in a narrow temperature window centered at about 1800°F.
Injection at higher or lower temperatures reduces NOx control efficiency significantly with
reduction dropping to near zero for deviations of more than about 100°F. Also, injection on
the cold side of the temperature window leads to bypassing of unreacted ammonia. In
practical combustion systems, the temperature of the combustion products varies both
spatially and temporally and it is difficult to design an injection system to avoid injection
outside of the temperature window.
The SNCR temperature window could be broadened to lower temperatures if an alternative
source of active radicals could be found. Previous investigators have evaluated addition of
hydrogen or hydrogen peroxide to ammonia, alcohols to urea, etc.; however, these additives
shifted rather than broadened the temperature window.
Integrating Reburning and SNCR: Advanced Reburning (AR). The AR process uses
reburning to enhance the SNCR process by providing OH radicals via the chain branching
reaction of CO oxidation. The reburning system is used to provide CO at the point of
ammonia (or urea) and overture air injection. The overfire air initiates the oxidation of CO:
CO + OH - CO2 + H, H + O2 - OH + O, and O + H2O - OH + OH. This chain
branching sequence provides additional OH radicals to initiate the NH3 oxidation sequence:
NH3 + OH - NH2 + H2O and NH2 + NO - N2 + H2O. The net effect is a broadening and
deepening of the SNCR temperature window on the cold side.
While the CO could be produced by operating the primary combustion system under oxygen
deficient conditions, such operation, particularly with coal, can seriously compromise the
combustion system and can lead to flame impingement, increased carbon loss, slagging, and
lower furnace tube wastage. With AR, the CO is provided via the reburning process; the
primary combustion system operates under conventional oxidizing conditions avoiding these
problems.
EER experimental studies1'2'16 demonstrated two AR approaches. One approach was to split
the overfire air in the reburning process into two streams. The first stream increases the
stoichiometry of the reburning zone to near stoichiometric conditions leaving some CO. The
remainder of the overfire air is injected with ammonia or urea to effect the SNCR
enhancement. The second and preferred approach is illustrated schematically in Figure 2.
The reburning zone is de-tuned from the normal substoichiometric conditions (about 0.9) to
near stoichiometric conditions where the CO is optimum for SNCR enhancement. The
overfire air is injected in a single stage further downstream with ammonia or urea. This
configuration avoids the complexity of two stages of overfire air and reduces the reburning
fuel injection rate by about half with significant cost benefits.
Figure 3 shows the results of AR tests conducted at 1.0 x itf Btu/hr in a coal fired test
furnace.2 The primary combustion zone was set up with NC^ at 890 ppm. Reburning was
used to reduce NOX to 470 ppm (47% reduction) and to vary the CO level at the point of
urea injection. As the CO level was increased, NOX decreased so as to broaden and deepen
the temperature window. Maximum NOX reduction was about 90%.
-------
Advanced Reburning Process Enhancements
Based on kinetic modeling and experimental studies, EER has recently developed two
enhancements to the AR process. They are: (1) the addition of "promoters" to the ammonia
or urea to improve the effectiveness of the NOx reduction, and (2) a method for injecting a
reagent into the reburning zone. These enhancements allow the AR process to be configured
in a number of new ways which offer reduced complexity and capital cost and/or improved
NOX control. This section discusses the results of initial tests of these enhancements and the
subsequent section shows how the enhancements can be incorporated into full scale high
efficiency AR based NOX control technologies.
N-agent Promotion. As discussed above, one constraint of the SNCR process is the
relatively narrow temperature window over which SNCR agents are effective. If the
temperature of the flue gas is too low at the point of injection, the NOX reduction efficiency is
low and ammonia slip will occur. If the temperature is too high, the SNCR agent tends to be
oxidized to produce NOX, and the net reduction of NOX is poor. In addition, injection of urea
or cyanuric acid often produces high emissions of N2O, a potential greenhouse gas which can
lead to degradation of the stratospheric ozone.
An experimental study was conducted at EER to investigate the promoted AR process. EER
patented inorganic salt promoters17 were tested hi a 1.0 x 106 Btu/hr combustion test rig to
determine their influence on the performance of AR with urea and ammonia. Figure 4 shows
some typical results for urea injection with a sodium promoter. The promoter significantly
extended the reaction window to lower temperatures and enhanced the NOX reduction
efficiencies. Close to 90% NOX reduction was achieved at 1700°F. Furthermore, the
promoter also dramatically reduced N2O emissions from urea as illustrated in Figure 5.
Reburning Zone Injection. A series tests were conducted in a combustion test rig at a firing
rate of 1.0 x 106 Btu/hr using natural gas as the fuel. The tests involved reburning with
injection of a reagent into the reburning zone. The specific injection method significantly
impacts the results and is confidential at this time. Three combustion configurations were
tested: single stage combustion (baseline), basic reburning using 10% reburning fuel injection
as in AR, and 10% reburning with reagent injection into the reburning zone. For all tests,
NO was measured after injection of burnout air at 1,800°F. Figure 6 shows the test results.
The initial uncontrolled NOX concentration was 530 ppm and reburning reduced NOX by 47%
to 280 ppm. Injection of the reagent into the reburning zone reduced NOX further. At a
reagent/NO stoichiometric ratio of 1.5, NOX was reduced by 78% from baseline and 58%
from the reburning level.
First and Second Generation Advanced Reburning Systems
Configurations and Projected NOX Control
The integration of reburning and SNCR can be configured into a number of AR processes
depending on how the following components are incorporated:
-------
• Reburning The rebuming process can be applied in the conventional configuration where
the reburning zone operates fuel rich for maximum N(\ control or can be de-tuned to
optimize a downstream SNCR process.
• Agent Injection Various agents can be injected into the reburning zone, with the overfire,
air, or downstream as in conventional SNCR.
The sections below discuss five AR configurations which offer a range of NOx control:
1. Advanced Reburning (Without Synergism)
2. Advanced Reburning (With Synergism)
3. Promoted Advanced Reburning (PAR)
4. Promoted Advanced Reburning -- Rich (PAR-Rich)
5. Multiple Injection Advanced Reburning (MAR)
The discussion addresses the plant modifications required and projected NO^ control
effectiveness based on extrapolation of the pilot scale test results. For ah1 cases, the reburning
system is assumed to be operated with 10% reburning fuel injection achieving 45% NO^
reduction from an uncontrolled level of about 500 ppm. Several figures are presented
showing applications of these AR systems to a generic front wall fired boiler. However,
since no modifications to the primary combustion system are required, the AR systems can be
applied to all firing configurations (wall, tangential, cyclone, and stoker). Another paper at
this symposium describes the basic reburning system common to all of the figures and
discusses the demonstrated performance of Gas Reburning ("Three Gas Reburning Field
Evaluations: Final Results and Long Term Performance" by B. Folsom et. al.).12 The reader
should recognize that the available data base on the AR process enhancements is limited.
Therefore, the NOX control projections should be considered preliminary.
Advanced Rebuming (Without Synergism). Figure 7 illustrates AR without synergism
applied to a generic wall fired boiler. This is the series application of reburning and
conventional SNCR. The SNCR agent is injected downstream of the overfire air ports in the
SNCR temperature window. Due to the narrow window of the basic SNCR process, the
incremental NOX reduction of SNCR is limited by available injection locations, mixing,
temperature gradients, and maximum acceptable ammonia slip. SNCR NOx reduction of 40%
has been assumed based on published SNCR results. The combined NOX control of the
system is nominally 77%.
Advanced Rebuming (AR). Figure 8 shows AR with synergism. The reburning process is
adjusted so as to produce a CO level at the end of the reburning zone great enough to broaden
and deepen the temperature window. The amount of reburning fuel injected is a sensitive control
variable which adjusts the CO level to alter the temperature window as operational conditions
vary. The SNCR agent effectiveness increases so that the combined NOX control increases to
nominally 85%.
In this configuration, the overfire air has a dual role: oxidation of the remaining CO and carrier
for the SNCR agent. The quantity of overfire air required depends on the amount of CO and the
-------
ability to mix the overfire air rapidly and completely with the furnace gases. Compared to
conventional reburning, where the stoichiometry is about 0.9, much less overfire air is required
for AR. It should be noted that the location of the overfire air ports may need to be moved
downstream to take maximum advantage of the temperature window broadening. However, since
the window is broad, the system designer has considerable flexibility in locating the ports to
avoid convective pass surfaces, buckstays, and other impediments.
Promoted Advanced Reburning (PAR). Figure 9 shows this process which is similar to AR
except that a promoter has been added to the SNCR agent. This increases the effectiveness of
the agent to about 90% and the total NOX control to about 95%. Since the promoter is water
soluble, supplying the agents in the form of water solutions (aqueous ammonia and urea in water)
are convenient. Thus, upgrading to PAR from AR is straightforward and requires no
modifications other than a mixing system for the promoter.
Promoted Advanced Reburning -- Rich (PAR-Rich). This process involves injection of a
reagent into the reburning zone as shown in Figure 10. The NOX control effectiveness is
somewhat reduced compared to the PAR process but is still comparable to AR. The advantage
of the PAR-Rich process is that the AR synergism is achieved independent of the overfire air.
This gives increased flexibility to locate the overfire air ports based on maximizing CO burnout
and with reduced concern over NOX control. In addition, it provides the opportunity for a second
stage of NOX control via promoted SNCR agent injection as discussed below.
Multiple Injection Advanced Reburning (MIAR). The highest NOX control is achieved by
using two injection stages as illustrated in Figure 11. In effect, this combines the PAR and Par-
Rich processes. The second injection stage boosts the total NOX control to nominally 98%.
Development and Demonstration Plans
EER's approach to the development and scale up of AR has paralleled that of Gas Reburning.
Gas Reburning was tested at firing rates up to 1.0 x 106 Btu/hr and a design methodology was
developed. That methodology was validated in tests at a larger scale, 10 x 106 Btu/hr. The
validated methodology was used to design three Gas Reburning systems for full scale utility units
and to project performance. Subsequent field tests confirmed the projected performance and
provides the basis for commercial applications to other units.
AR was tested initially at the 1.0 x 106 Btu/hr scale in a combustion test rig. A design
methodology was assembled and its performance predictions were confirmed in subsequent tests
at the 10 x 106 Btu/hr scale in another test rig. Therefore, EER believes that AR is now ready
for a full scale installation. The candidate demonstration site is the Tennessee Valley Authority
Allen Station which has three 330 MW cyclone fired boilers. EER has applied the design
methodology to the Allen units and projected 85% NOX control for first generation AR. EER
is now conducting a more detailed evaluation under contract to TVA. TVA will use the results
of this evaluation as part of their decision process to select the best approach for NCx control
at the station.
-------
The second generation AR process enhancements have been only tested briefly at a firing rate
of 1.0 x 10s Btu/hr. While the results are promising, additional development work is required.
The Department of Energy has selected HER to proceed with the second generation development
in a comprehensive two phase project. The work is scheduled to commence in September 1995.
The goals will be to provide sufficient short term development to provide a data base for
upgrading the first full scale AR demonstration to the second generation technology.
Conclusions
In conclusion, reburning and SNCR can be integrated together synergistically in a number of
configurations. The basic AR process uses reburning to broaden the SNCR temperature window
with the potential for NOX control in the range of 85%. This first generation technology is ready
for full scale field demonstration. Two process enhancements have been identified which
increase the flexibility of the AR process and increase its NOx control potential to over 95%.
These enhancements require additional development. These AR systems are alternatives to SCR
and should be of significant value to combustion system operators faced with Post-Ract NC^
reductions in ozone non-attainment areas.
References
1. S. L. Chen, et. al., "Optimization of Reburning for Advanced NOX Control on Coal-fired
Boilers," Journal of the Air & Waste Management Association, Volume 39, Number 10,
pp 1375-1379 (1989).
2. S. L. Chen, et. al., "Advanced Non-Catalytic Post Combustion NOX Control,"
Environmental Progress, Volume 10, Number 3, pp 182-185, (1991).
3. J. O. L. Wendt et. al., "Reduction of Sulfur Trioxide and Nitrogen Oxides by Secondary
Fuel Injection, "Fourteenth Symposium (International) on Combustion, pp. 897-904,
(1973).
4. J. A. Miller and C. T. Bowman, "Mechanism and Modeling of Nitrogen Chemistry in
Combustion.", Progress in Energy and Combustion Science, Volume 15, p. 287 (1989).
5. A. Sanyal et. al., "Cost Effective Technologies for SO2 and NOX Control," presented at
Power-Gen '92, Orlando, Florida (November 17-19, 1992).
6. B. A. Folsom, et. al., "Reducing Stack Emissions by Gas Firing in Coal-Designed Boilers
~ Field Evaluation Results," presented at the EPRI/EPA 1993 Joint Symposium on
Stationary Combustion NOX Control, Miami Beach, Florida (May 24-27, 1993).
7. C.C. Hong et. al.,"Gas Reburning and Low NOX Burners on a Wall-Fired Boiler,"
presented at the Second Annual Clean Coal Technology Conference, Atlanta, Georgia
(September 7-9, 1993).
8. R. T. Keen, et. al., "Enhancing the Use of Coal by Gas Reburning and Sorbent Injection,"
presented at the Second Annual Clean Coal Technology Conference, Atlanta, Georgia
(September 7-9, 1993).
9. A. Sanyal et. al., "Advanced NOX Control Technologies," presented at the Tenth Annual
International Pittsburgh Coal Conference (September 20-24, 1993).
10. A. Sanyal et. al., "Gas Reburning for NOX Reduction - An Integrable Cost Effective
technology for International Applications," presented at the Clean Fuel Technology
Conference, London, UK (May 19, 1994).
-------
11. T. J. May, "Gas Retraining in Tangentially, Wall, and cyclone fired boilers -- An
Introduction to Second Generation Gas Reburning," presented at the Third Annual Clean
Coal Technology Conference, Chicago, Illinois (September 6-8, 1994).
12. B. A. Folsom, et. al., "Three Gas Reburning Field Evaluations: Final Results and Long
Term Performance," presented at the EPRI/EPA 1993 Joint Symposium on Stationary
Combustion NOX Control, Kansas City, Missouri (May 16-19, 1995).
13. R. K. Lyon, "Method for the Reduction of the Concentration of NO in Combustion
Effluents Using Ammonia," U.S. Patent No. 3,900,554 (August 19, 1975).
14. R. K. Lyon and J. E. Hardy, "Discovery and Development of the Thermal DeNOx
Process.", Industrial and Engineering Chemical Fundamentals, Volume 25, Number 19
(1986).
15. J. K. Arand, et. al. Muzio, LJ. and Softer, J.G., U.S. Patent Number 4,208,386 (June
17, 1980).
16. W. R. Seeker, et. al., "Advanced Reburning for Reduction of NOX Emissions in
Combustion systems," U.S. Patent No. 5,139,755 (August 18, 1992).
17. L. Ho, et. al., "Methods for Controlling N2O Emissions and for the Reduction of NOx and
SOX Emissions in Combustion Systems While Controlling N2O Emissions," U. S. Patent
No. 5,270,025 (December 14, 1993).
-------
c
PRIMARY
ZONE
Low Excess Air
t
>l
|NOX~90%
4-
REBURNING
ZONE
Slightly Fuel Rich
NOX -40%
BURNOUT
ZONE
Normal Excess Air
Figure 1
The Rebuming Process
|NOX -40%
-60% NOX
Reduction
PRIMARY
ZONE
Low Excess Air
t
NOX -90%
*•
c
REBURNING
ZONE
Near Stoichiometric
J^
leburn
NOX -50%
CO-1000 ppm
C
BURNOUT
ZONE
Normal Excess Air
Figure 2
The Advanced Rebuming (AR) Process
NOX~15%
-85% NOX
Reduction
-------
NO Remaining (%)
1UU -
on '
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From :
Gas 60 :
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(470 ppm) 4ft :
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1500
1-q
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Final NOX Q
Initial NOX Q
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8-
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-10
r\
From
Baseline
(890 ppm)
Ill 1 1 1 1 III III T [" 1 T" 1 "!—' U
1600 1700 1800 1900 2000
Injection Temperature (F)
FigureS
NOX Control Via Advanced Reburning (AR)
• "•
^^
TTri-"
V n
\ Urea
\ Only
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\
\UlL-U tiuu \
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1400 1600 1800
Injection Temperature °F
Figure 4
NO Control Via Promoted Urea Injection
2000
-------
N20 (ppm)
Urea and
Sodium
Promoter
10
0
1400
1600 1800
Injection Temperature °F
2000
Figure 5
N2O Reduction Via Promoted Urea Injection
NOX 300
(ppm)
Baseline NOY = 530 ppm
10% Rebuming NO = 280 ppm
0.5 1 1.5 2 2.5
Reagent / NO Stoichiometric Ratio (molar ratio)
Figure 6
NOX Control Via Reagent Injection into the Rebuming Zone
-------
SNCR
Agent
Reburning
Fuel (-10%)
Baseline
Reburning
SNCR agent
NOx
Reduction (%)
03
•4_J
o
45
40
45
67
Figure 7
Advanced Reburning (AR) Without Synergism
x
§
bO
'3
100
55
33
SNCR
Agent
Reburning
Fuel (-10%)
Baseline
Reburning
SNCR agent
Figure 8
Advanced Reburning (AR) With Synergism
NOx
Reduction (%)
03
S
o
45
13
o
H
45
85
g,
x
O
c
"o3
g
100
55
15
-------
Promoted
SNCR
Agent
Rebuming
Fuel (-10%)
•
t^^ Baseline
"^^ Rebuming
Promoted SNCR agent
NOx
Reduction (%)
1
|
o
HH
--
45
90
o
H
--
45
95
X
O
£
M
Remain
100
^55
5
Figure 9
Promoted Advanced Rebuming (PAR)
Reagent
Rebuming
Fuel (-10%)
»*
. ^y Baseline
^^^^ Rebuming
^ Reagent
NOx
Reduction (%)
"c
2
o
HH
45
70
13
•4— >
£
--
45
84
^
X
O
bO
C
Remain
,100
55
16
Figure 10
Promoted Advanced Rebuming -- Rich (PAR-Rich)
-------
Promoted
SNCR
Agent
Reagent
Reburning
Fuel (-10%)
V^ Baseline
^^^ Reburning
^^ Reagent
kPromoted SNCR agent
NOx
Reduction (%)
Incremental
--
45
70
90
IS
o
H
--
45
84
98
Remaining NOx (%)
100
55
16
2
Figure 11
Multiple Injection Advanced Reburning (MIAR)
-------
THE USE OF PULVERIZED COAL AND COAL-WATER-SLURRY
IN REBURNING NOX CONTROL
Roy Payne, David K. Moyeda, and Peter Maly
Energy and Environmental Research Corporation
18 Mason
Irvine, California 92718
Tanya Glavicic
Canadian Electrical Association
1 Westmount Square, Suite 1600
Montreal, Quebec, Canada H3Z 2P9
Bill Weber
Electric Power Research Institute
3412 Hillview Avenue
Palo Alto, California 94304
Abstract
Reburning is a NOX reduction technique which has been demonstrated on a number
of coal-fired utility boilers. Unlike alternative control techniques such as low NOX
burners and selective non-catalytic reduction, reburning can achieve high levels of
control without increasing carbon-in-ash and without measurable by-product
emissions. In the application of reburning, a wide range of fuels can be used in the
process, including natural gas, fuel oil, and coal. This paper describes the results of
pilot-scale studies to investigate the parameters influencing the use of coal-based
fuels in the reburning process. Different pulverized coals, and coal-water-slurries
made from recovered coal fines, were evaluated as potential reburning fuels in a
pilot-scale facility designed to simulate representative boiler conditions. Results of
these studies have confirmed the viability of coal as a reburning fuel in either
pulverized or slurry form. The sub-bituminous and lignitic coals tested showed the
potential to achieve high levels of NOX control, while performance with
bituminous coals tended to be related to fuel nitrogen content and volatility. With
all coals, reburning performance was also found to be strongly influenced by
available residence time and by initial NOX levels. The test results provide insight
into the impacts of coal type and properties on the reburning process and provide
critical information needed to optimize the use of coal-based fuels in application of
reburning to utility boilers.
-------
Introduction
Throughout the world, regulations are being implemented to control acid rain
precursors such as sulfur and nitrogen oxides from coal-fired utility boilers.
Therefore, there is increasing interest in the development and application of cost
effective technologies for controlling these emissions. Reburning is one technology
which is particularly effective at controlling NOX emissions and which can be easily
retrofit to existing utility boilers. The key advantages of reburning over other NOX
control technologies are that: 1) it provides high levels of NOX control; 2) it can be
implemented without significant impacts on boiler performance or carbon in ash; 3)
it produces no by-product emissions; and 4) it can be applied to all types of boilers,
including tangentially fired, wall-fired, and cyclone-fired boilers.
In the reburning process, fuel is injected above the main combustion zone to
provide a slightly fuel rich environment or "reburning zone" which reduces
nitrogen oxides formed in the primary combustion zone to molecular nitrogen.
Following the reburning zone, additional combustion air is added to the boiler to
oxidize carbon monoxide and any remaining fuel fragments exiting the reburning
zone. Small-scale studies have shown that any hydrocarbon fuel can be used in the
process, including natural gas, fuel oil, or coal1/2. In the United States, several
demonstrations of the application of natural gas reburning on coal-fired utility
boilers have been completeds, 4. in addition, there is interest in the application of
reburning technology to utility boilers throughout the world5.
Natural gas has many advantages as a reburning fuel in that it contains no fuel
nitrogen and that combustion occurs readily, making it ideal for retrofit applications
with limited access and limited combustion space. However, natural gas is generally
more expensive than coal, and there may be significant technical and cost benefits to
using coal and coal-based fuels as the reburning fuel where this may be viable. In
considering the application of coal reburning to a specific boiler, one critical issue is
the way in which coal properties influence NOX reduction levels achievable, and the
impacts of coal properties on boiler performance. Understanding these effects is
essential to optimizing the process for boiler applications.
Coal is a nitrogen bearing fuel, and the extent to which this factor and other coal
properties are expected to impact overall reburning effectiveness will depend
primarily upon fuel nitrogen content and nitrogen reactivity. In the retrofit of
reburning to an existing boiler, complete combustion of the reburning fuel is always
a concern because of the limited time and temperature available for reactions to
occur. Because coal does not burn as readily as natural gas, coal reburning also has
the potential to increase unburned carbon losses. In addition, coal ash can slag under
fuel-rich conditions leading to increased deposits on the boiler walls in the reburn
zone. Therefore, the use of some coals in specific boiler situations may be
unacceptable from a boiler operability point of view.
-------
In the application of coal reburning to a particular boiler, there are several fuel
alternatives to consider. The coal used in the reburning process could be the same as
the coal fired under normal conditions, or it could be a coal which is selected to yield
improved NOX control performance with reduced boiler impacts in comparison to
the nominal plant coal. Tailoring the coal to fit site specific requirements could
benefit a utility's overall compliance plan. A third reburning fuel alternative for
consideration is the use of coal-water-slurry, which could be formed from the
nominal plant coal, or from coal fines recovered from a coal cleaning process.
Although this latter approach is very site specific, the use of coal fines in the form of
coal-water-slurry could provide environmental benefits and reduce fuel and NOX
control costs6.
This paper describes the results two separate investigations into the impacts of coal
properties on the effectiveness of the reburning process. These investigations,
sponsored by the Canadian Electrical Association and the Electric Power Research
Institute-Upgraded Coal Interest Group, were focused on evaluating the feasibility
of using coals of various rank and coal water slurries as reburning fuels in coal-fired
utility boilers. The three primary objectives of these studies were: (1) to develop an
experimental data base on the performance of coals and coal-water slurries under
reburning conditions; (2) to determine the operating conditions which are necessary
for optimization of the use of coal-based fuels in the reburning process, with respect
to maximizing NOX reduction and carbon burnout; and (3) to assess the potential
impacts of coal characteristics on performance and the resulting implications for
full-scale application.
In these studies, a number of different pulverized coals and coal water slurries made
from recovered coal fines were evaluated as potential fuels for reburning
application to coal-fired utility boilers. Twelve coals were tested in a small
pilot-scale facility designed to simulate representative boiler conditions, and with
sufficient flexibility to cover an effective range of process parameters. The coals
tested in the study were selected based upon their representativeness as coals which
are likely to be best used as reburning fuels from the standpoints of lowest NOX
emissions, lowest impact on boiler performance, and highest probability of use by
utilities in Canada and the Eastern United States. Each of the coals and coal water
slurries were evaluated as reburning fuels over a range of conditions typical of
coal-fired utility boilers. Experimental conditions were defined following a brief
survey of utility boiler design and operational characteristics, where key parameters
such as uncontrolled NOX emissions, local temperatures, quench rates, and
residence times were identified, relative to specific coal types.
In the following sections of this paper, the general impacts of process parameters
and fuel properties on the performance of the reburn process using coal-based fuels
will be described, and the results of the experimental studies and their implications
for full-scale application will be discussed.
-------
Reburning for NOX Control
Reburning is a combustion modification technology which removes NOX from
combustion products by using fuel as a reducing agent. The fundamental principle
of this technology— that fuel fragments can react with NO to form molecular
nitrogen—has been studied for over two decades. The reburn process has been
extensively evaluated at bench, pilot and full scale to identify the parameters which
control process performance*- 2> 7> 8- 9. The results of these studies have shown that
the most critical parameters which impact reburning performance are: primary NOX
level; reburning zone temperature and residence time; and reburning zone
stoichiometry. In general, reburning effectiveness improves with increasing
primary NOX level, and with increasing reburn zone temperature and residence
time. For utility boilers, the optimal stoichiometry for the reburning zone generally
corresponds to the addition of a quantity of reburn fuel equivalent to about 20
percent of the total boiler heat input. In practical applications of the process, mixing
of the reburning fuel, and the overfire air, with the bulk furnace gases is also an
important consideration.
In the use of coal and coal-based fuels as reburning fuels, a significant question is
the extent to which fuel bound nitrogen and other coal properties influence NOX
reduction effectiveness. Previous studies using coal as a reburning fuel have
suggested that the suitability of a coal for reburning depends upon fuel volatility,
nitrogen content, and nitrogen reactivity. Fuel volatility impacts the availability of
fuel in the reburn zone and, hence, the evolution of radical species. As a result, fuels
with a higher volatile content would be expected to attain higher levels of NOX
reduction. Fuel nitrogen can also have an impact on reburning effectiveness since
the addition of reactive nitrogen species to the reburning zone can influence the
final emissions levels attained. Generally, fuel nitrogen content becomes more
critical at lower initial NOX levels. The distribution of nitrogen in the volatile
matter and char is also important, since nitrogen species released with the volatile
matter have more opportunity to be reduced to molecular nitrogen. During
burnout, nitrogen in the char can be oxidized, or it may play a role in heterogeneous
NOX reduction^.
In application of coal reburning to utility boilers, there are also concerns about the
impacts of the process on carbon burnout and slagging and fouling in the reburning
zone. A key consideration is the impact of available residence time on the process
performance and on carbon burnout. The impacts of coal properties on carbon
burnout and slagging and fouling are expected to be coal and boiler specific. The use
of computational models for predicting these impacts and for developing strategies
to mitigate their influence is expected to be a key step in full-scale applications of
the technology. To this end, HER is currently adapting existing reburning and boiler
performance models to accommodate the data obtained in these studies and to
extrapolate performance to possible utility applications.
-------
Test Results
Reburning experiments were conducted in a 1.0 MMBtu/hr pilot-scale test facility,
which is shown in Figure 1. The test facility consists of a down-fired refractory lined
combustion tunnel followed by a convective pass simulator and baghouse. To
facilitate evaluation of the test coals on a consistent basis, the primary fuel was
natural gas which was fired at 800,000 Btu/hr with ten percent excess air. Initial NOX
emissions from the primary flame were controlled to set levels between 200 and
1300 ppm (dry, corrected to 3%O2) by premixing ammonia with the combustion air.
The returning fuels were all injected at an initial temperature between 2600 and
2700°F. Nitrogen, which simulates recirculated flue gas, and air were used as the
transport carrier for the pulverized coals, and as the atomization media for the coal
water slurries. Burnout air was injected downstream of the reburning fuel to bring
the overall furnace stoichiometry up to twenty percent excess air. The burnout air
injection location was set to provide a reburn zone residence time between 200 and
1200 milliseconds. The thermal profile in the furnace was set to provide a quench
rate in the reburning zone of approximately 350°F per second.
Ten coals were selected from a data base of coals commercially available in Canada
and the United States using a methodology where the coals were ranked according
to their NOX reduction potential, slagging potential, carbon burnout potential, and
then according to their relative usage. The methodology was developed using
weighted coal properties to determine ranking criteria for each coal. Two
bituminous coals, from the Eastern United States, were selected based upon their
potential use in coal cleaning processes. The ranges of selected properties of the test
coals are summarized in Table 1, where the coals are classified by rank.
The coals shown in Table 1 were tested over a range of reburning zone
stoichiometric ratios corresponding to reburning fuel heat inputs between 10 to 40
percent of the total heat input. Results for the pulverized coals are summarized in
Figure 2. Also shown in this figure are the results of using natural gas as a reburning
fuel. Generally, each of the pulverized coals exhibited an optimum NOX reduction at
a reburning fuel heat input of 20, when nitrogen was used as the transport medium.
At this level of heat input, the NOX reduction achieved with pulverized coal ranged
from 40 to 60 percent, with some coals displaying performance equivalent to that of
natural gas under the same nominal conditions. The variations in performance
achieved illustrates the potential impact of coal properties on the process.
The NOX control performance measured with coal-water-slurry as a reburn fuel is
shown in Figure 3. This figure compares the results obtained with a bituminous
coal, where the coal was introduced to the reburn zone in either pulverized or
slurry form. In addition, tests were performed where water (as steam) was added to
the pulverized coal prior to injection into the reburning zone. The results shown in
Figure 3 indicate that there is little influence of the water addition, and suggest that
the method of introducing the coal has little impact on the NOX reduction
-------
performance. These results confirm the viability of using coal-water-slurry in the
reburning process.
Figures 4 and 5 illustrate the impacts of initial NOX level and reburning zone
residence time on reburning effectiveness. In agreement with previous studies, the
data shown in these figures demonstrate that the performance of the reburning
process increases at higher initial NOX levels and longer reburning zone residence
times. In addition, these results indicate that the actual performance which can be
achieved with a specific coal is influenced by its properties. In comparison to the use
of natural gas as a reburning fuel, where high NOX reduction efficiency can be
achieved at low initial NOX levels and at reburning zone residence times as short as
200 milliseconds, the performance of coal reburning drops off significantly at initial
NOX levels below 400 ppm and reburning zone residence times below about 500
milliseconds. For the coals and conditions investigated in these studies, the
effectiveness of the reburning fuel decreases as the initial NOX level and reburning
zone residence time are reduced due to the impacts of fuel nitrogen added to the
reburning zone with the coal and to the impacts of fuel volatility on the reburning
process.
In the application of coal reburning to utility boilers, the selected transport medium
could be air or recycled flue gas. The impact of the transport media on the
performance coal reburning is shown in Figure 6. In these tests, nitrogen was used
as the inert carrier to simulate recycled flue gas. The comparison of air verses
nitrogen transport shown in Figure 6 indicates that there are two important factors
to consider when selecting the transport medium. First, the use of a transport media
containing high levels of oxygen requires the addition of a higher percentage of the
heat input to reach the optimum level of NOX control. Second, the presence of high
levels of oxygen in the transport can reduce the optimum performance achieved
with a specific fuel. Since the addition of oxygen to the transport media requires
additional reburning fuel in order to consume the additional oxygen, the need to
increase the reburning fuel heat input is understood; however, the factors
contributing to a reduction in the effectiveness of the process are not clear at this
time. In general, all of the pulverized coals and coal water slurries tested appear to
be affected in the same fashion, but to a greater or lesser extent depending upon the
fuel properties. In addition, the performance of a specific fuel appears to be more
sensitive to the effects of oxygen in the transport medium as initial NOX level and
reburning zone residence time are decreased.
From the data presented above, it is clear that coal properties can have a significant
impact on reburn NOX reduction performance. Although the experimental data
suggest that fuels with low nitrogen content and high volatility are better
performers, NOX reduction potential does not readily correlate with either of these
parameters. In order to better account for coal composition, a ranking parameter has
been developed which combines coal volatile content, fixed carbon, and fuel
nitrogen, into a value which reflects the ease with which fuel nitrogen is released
into the gas phase. A coal with a high ranking may, for example, be high in fuel
-------
nitrogen and low in volatile content. The use of the ranking parameter in the
presentation of optimum NOX reduction data for the different coals is illustrated in
Figures 7 and 8. The figures present data for inert and air as the transport medium,
respectively, and for combinations of different reburn zone residence times and
initial NOX values.
For inert reburn fuel transport medium (i.e., nitrogen), Figure 7 shows that,
although there is some considerable scatter in the data, there is a good preliminary
indication that the general trends observed are accounted for. For bituminous coals
in particular, NOX reduction performance falls off significantly with higher values
of the ranking parameters. The sub-bituminous and lignitic coals tested appear,
however, to be less influenced by coal properties, and NOX reduction performance
seems to reach an asymptote which is related more to local operating conditions. At
higher initial NOX levels and longer reburn zone residence times, the data in Figure
7 reflect the significant increase in NOX reduction discussed earlier. An
improvement of some 15 percentage points appears to accrue due to these more
favorable operating conditions. Unfortunately, insufficient test data were obtained
for the lower rank coals to determine whether performance again reached an
asymptote at the higher NOX reduction levels.
Similar trends in the data are also found when air is used as the reburn fuel
transport medium, as shown in Figure 8. Again, there is some considerable scatter
in the data, but the general trends established with inert transport appear to hold. In
comparing the results of Figures 7 and 8, it is clear that NOX reduction performance
is significantly reduced when using air to transport and inject the reburn fuel. The
magnitude of this effect is equivalent to some 10 percentage points of NOX reduction
at low initial NOX and residence time, and to about 7 percentage points at higher
initial NOX and longer times.
A further consideration in the actual application of coal reburn technology to utility
boilers is carbon loss. Figure 9 shows the loss on ignition results obtained for the
pulverized coals which were tested. As might be expected, bituminous coals showed
the highest carbon loss, while low rank coals had the lowest carbon loss. The
burnout achieved with the bituminous coals appeared to be sensitive to coal volatile
content. Burnout achieved with the low rank coals, however, was not sensitive to
coal volatile content over the range of this parameter evaluated in this study.
Conclusion
The primary objective of these studies was to determine the potential for using
coal-based fuels in the application of the reburning process to coal-fired utility
boilers, and to assess the factors which most influence process performance. The
results of pilot-scale tests conducted with coals of different rank indicate that NOX
reductions between 40 to 60 percent should generally be attainable with coal
reburning under typical utility boiler conditions. In addition, the results of the tests
-------
show that the coal can be introduced in pulverized or slurry form without
impacting the process effectiveness. Therefore, the use of coal-water-slurries made
from recovered coal fines as reburning fuels is expected to be a viable technique for
reducing NOX emissions.
The level of NOX reduction performance which can be achieved with coal reburning
in practice will be controlled by site specific factors such as initial NOX level and the
available reburning zone residence time, by the method with which the reburning
coal is transported and injected into the furnace, and by the properties of the coal
used as a reburning fuel. In evaluating the impact of parameters such as nitrogen
content and volatile matter content on the effectiveness of the coals, it was found
that bituminous coal performance, in terms of NOX reduction, improved with
decreasing nitrogen content and increasing volatile content. Carbon burnout for
bituminous coals also improved with increasing coal volatile content. However,
these parameters were not able to correlate the NOX reduction or carbon burnout
performance of the low rank coals evaluated.
Acknowledgments
The work presented in this paper was sponsored by the Canadian Electrical
Association (CEA), and the Electric Power Research Institute-Upgraded Coal Interest
Group (EPRI-UCIG), with co—funding provided by the Tennessee Valley Authority
(TVA). The authors would like to acknowledge the technical direction provided by
the CEA project technical monitors: Mr. Dilip Deshpande of Alberta Power, Dr.
Horace Whaley of CANMET, and Mr. Edmundo Vasquez of Ontario Hydro
Research. The technical assistance of Mr. George Lee is also gratefully acknowledged.
References
1. Chen, S. L., et al. NOX Reduction by Reburning with Gas and Coal — Bench Scale
Studies. Proceedings of the 1982 Joint Symposium on Stationary Combustion
NOX Control, Volume 1: Utility Boiler Applications, EPRI Report No. CS-3182,
Volume 1, Electric Power Research Institute, Palo Alto, California, July 1983.
2. Chen, S. L., et al. Bench and Pilot Scale Process Evaluation of Reburning for
In-Furnace NOX Reduction. Twenty-First Symposium (International) on
Combustion, The Combustion Institute, pp. 1159-1169, 1986.
3. Folsom, B. A., Sommer, T. M. and R. Payne. Demonstration of Combined NOX
and SO2 Emission Control Technologies Involving Gas Reburning. Presented at
the AFRC/JFRC International Conference on Environmental Control of
Combustion Processes, Honolulu, Hawaii, 7-10 October 1991.
-------
4. May, T. J., et al. Gas Reburning in Tangentially, Wall-, and Cyclone-Fired
Boilers. An Introduction to Second-Generation Gas Reburning. Presented at the
Third Annual Clean Coal Technology Conference, Chicago, Illinois, 6-8
September 1994.
5. Proceedings of the Gas Research Institute/Swedish Gas Center/Danish Gas
Technology Center International Gas Reburn Technology Workshop, Malmo,
Sweden, 7-8 February 1995.
6. Melick, T., et al. Co-Firing Conventional and Upgraded Coal-Water Slurry in
Utility Boilers. Reduced NOX Emissions to Increase Operating Compliance
Margin. Presented at the 20th International Technical Conference on Coal
Utilization & Fuel Systems, Clearwater, Florida, 20-23 March 1995.
7. Greene, S. B., et al. Bench Scale Process Evaluation of Reburning for In-Furnace
NOX Reduction. ASME Journal of Engineering for Gas Turbines and Power,
Volume 108, pp. 450-454,1986.
8. Overmoe, B. J., et al. Pilot Scale Evaluation of NOX Control from Pulverized Coal
Combustion by Reburning. Proceedings of the 1985 Joint Symposium on
Stationary Combustion NOX Control, Volume 1: Utility Boilers Applications,
EPRI Report No. CS-4360, Volume 1, Electric Power Research Institute, Palo
Alto, California, 1986.
9. Payne, R. And D. K. Moyeda. Scale Up and Modelling of Gas Reburning. ASME
FACT-Volume 18, "Combustion Modeling, Scaling and Air Toxins", A. K. Gupta
et al., editors, pp. 115-122,1994.
10. Chen, W. Y. and T. W. Lester. Effects of Reburning Fuel Type on NOX Reduction.
Presented at the Eighth Annual Coal Preparation, Utilization, and
Environmental Control Contractors Conference, Pittsburgh, Pennsylvania, July
27-30,1992.
-------
TABLE 1. PROPERTIES OF COAL-BASED REBURNING FUELS.
Coal Type
Proximate (wt. %):
Moisture
Ash
Volatiles
Fixed Carbon
Nitrogen (wt. %, daf)
HHV (Btu/lb)
Bituminous
Coals
1.80 - 3.39
5.82 - 12.45
32.93-35.52
50.91-54.07
1.11 -1.43
11,661 - 14,075
Sub-Bituminous
Coals
4.83 - 6.59
11.47-18.96
29.63-36.8
44.85-48.37
0.94 - 1.29
9,404 - 10,111
Lignite
Coals
10.64 - 19.34
14.82 - 15.97
31.26-43.22
31.32-33.43
0.92-1.31
7,495-9,048
Coal Water Slurry
Parent Coals
7.07 - 7.34
8.33 - 12.97
25.15-37.00
47.07 - 54.81
1.70-1.77
12,281 - 12,477
Figure 1. Schematic of pilot scale test facility.
-------
80
60
o
Pulverized Coal
Nitrogen Transport
Initial NO~400ppm
Reburn Zone - 400 msec
0
Natural Gas
(Typical) v
Reburn Fuel:
O Bituminous
• Sub—Bituminous
X Lignite
i i i , i , ,
10 15 20
Reburn Fuel Heat Input, %
25
30
Figure 2. NOx reduction performance of coals used as reburning fuel.
80
60
Bituminous Coal
Nitrogen Transport/Atomization
Initial NO ~ 600 ppm
Rebum Zone - 600 msec
0
Reburn Fuel Form:
O Pulverized Coal
• Pulverized w. Water Doping
B Coal Water Slurry
, i , i i i i , i i i
10 15 20
Reburn Fuel Heat Input, %
25
30
Figure 3. Performance comparison of means of injecting reburning coal.
-------
c
o>
DC
c
3
fj
O
DC
100
80
60
40
20
Air Transport/Atomization
Rebum Heat Input ~ 20%
Natural Gas
(Typical)
Reburn Fuel:
O Bituminous (400 ms)
A Bituminous (400 ms)
• Sub-Bituminous (600 ms)
X Lignite (600 ms)
E Coal Water Slurry (600 ms)
i , , , i i , , i , , ,
200 400 600 800
Initial NO, ppm
1,000 1,200
1,400
Figure 4. Impact of initial NOx level on reburn performance.
o
o
3
T3
03
DC
.o
o>
DC
100
80
60
40
20
Air Transport/Atomization
Reburn Heat Input - 20%
Natural Gas
(Typical)
B
Reburn Fuel:
O Bituminous (600 ppm)
A Bituminous (600 ppm)
• Sub-Bituminous (400 ppm)
* Lignite (400 ppm)
B Coal Water Slurry (600 ppm)
. . . i . , , i . . .
200 400 600 800 1,000
Reburn Zone Residence Time, msec
1,200 1,400
Figure 5. Impact of reburn zone residence time on reburn performance.
-------
80
60
c
g
01 40
ox
.a
IT 20
Pulverized Bituminous Coal
Initial NO - 400 ppm
Reburn Zone - 400 msec
Transport:
OAir
• Inert (Nitrogen)
10 20 30 40
Reburn Fuel Heat Input, %
50
Figure 6. Impact of transport medium on coal reburn performance.
3^
.0
f
DC
X
O
1
JD
03
oc
ou
70
Cf\
bU
50
40
30
20
in
n
- Inert Transport/Atomization
Rebum Heat Input ~ 20% "'\ *
O**
^^ f600 msec, 600 ppm)
** ^"":^
* *s \
/ * >f ..
^400 msec, 400 ppm) ^*^^^ N^ *p^
•\ °
>v
^
. Rebum Fuel:
X* Sub-Bituminous/Lignite, PC
•O Bituminous, PC
• BD Bituminous, CWS
i 1,1,1,1,1,
2.0 2.2 2.4 2.6 2.8 3.0 3.2
Coal Ranking Parameter - /(Volatiles, Fixed Carbon, Fuel N)
3.4
Figure 7. Correlation of coal reburn performance using inert transport.
-------
g
"o
T3
0>
rr
X
O
3
.a
a>
CC
80
70
60
50
40
30
20
10
Air Transport/Atom ization
Reburn Heat Input - 30%
(400 msec, 400 ppm)
Reburn Fuel:
X* Sub-Bituminous/Lignite, PC
•O Bituminous, PC
•D Bituminous, CWS
, . , , i i , , , i , , , , i
(600 msec, 600 ppm)
2.0 2.2 2.4 2.6 2.8 3.0 3.2
Coal Ranking Parameter - /(Volatiles, Fixed Carbon, Fuel N)
3.4
Figure 8. Correlation of coal reburn performance using air transport.
16
12
_o
> 8
o
CO
CO
o
Pulverized Coal
Nitrogen Transport
Reburn Heat Input - 20%
Lignite
Sub-Bituminous
Bituminous
Reburning Coal Type
Figure 9. Carbon burnout performance of reburn coals.
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Three Gas Reburning Field Evaluations:
Final Results and Long Term Performance
Blair Folsom and Todd Sommer
Energy and Environmental Research Corporation (EER)
18 Mason
Irvine, California 92718
Harry Ritz
U. S. Department of Energy, Pittsburgh Energy Technology Center
P.O. Box 10940
Pittsburgh, Pennsylvania 15236
John Pratapas and Paul Bautista
Gas Research Institute
8600 West Bryn Mawr Avenue
Chicago, Illinois 60631
Tony Facchiano
Electric Power Research Institute
3412 Hillview Avenue
Palo Alto, California 94304
Abstract
Gas Reburning (GR) is a NOX control technology for boiler/furnace applications. Natural gas
is injected above the burner zone to produce a slightly fuel rich zone where NOX may be
reduced by 60-70%. Overfire air completes the gas combustion. Three comprehensive GR
demonstrations have been completed on U.S. utility boilers as part of the Qean Coal
Technology Program. The boilers included tangential, wall, and cyclone configurations firing
coal with capacities of 33-158 MW net. Two of the units were tested firing 100% gas as the
primary and reburning fuels and on one unit GR was integrated with low NOX coal burners.
One of the demonstrations included first and second generation GR designs. The second
generation improvements included elimination of flue gas recirculation (FGR) as the natural
gas carrier and dual concentric overfire air ports. Data are presented showing both parametric
test results and long term performance in normal utility service. NOX reductions up to 76%
and NO, levels as low as 0.05 lb/106 Btu (on 100% gas) were achieved with no significant
operational impacts.
Introduction
The oxides of nitrogen, collectively referred to as NO*, are widely recognized as air
pollutants for three primary reasons. First, they are themselves toxic; second, in the
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atmosphere they can combine with moisture to produce nitric acid which can precipitate as
acid rain; third, hi the presence of sunlight NOx can react with hydrocarbons to produce
photochemical smog and ozone. Under Title I of the Clean Air Act Amendments of 1990
(CAAA), NOX control is required to mitigate ozone non-attainment areas. The requirements
for each ozone non- attainment area are being established based on the severity of the problem
and the local emission inventory. In many areas NOx control to levels deeper than those
achievable with low NOX burners will be required.
Gas Reburning (GR) is a combustion modification NOx control technique which can be
retrofitted to a wide range of combustion equipment to achieve deeper NOx control than that
of low NOX burners. By itself, for applicable units, GR is capable of achieving NOx
reductions on the order of 60% or more. In addition, GR can be combined with other NOx
control technologies, such as low NOX burners, for even deeper control.
This paper presents the test results from GR installations on three coal fired utility boilers.
The design, installation and testing of the GR systems was conducted by Energy and
Environmental Research Corporation (EER) as part of the U.S. Department of Energy Clean
Coal Technology Program.1'2 Several organizations provided cofunding support to make this
project possible including the Gas Research Institute, the Electric Power Research Institute,
the State of Illinois Department of Energy and Natural Resources, Colorado Interstate Gas,
and three host utilities: Illinois Power, City Water, Light and Power, and Public Service
Company of Colorado.
On two of the units, GR was integrated with Sorbent Injection (SI) for combined NO^ and
SO2 control.1 On the third unit, GR was integrated with conventional low NOX burners.2
EER used its design methodology to optimize the GR configurations for each unit and to
project both NOX control and boiler performance.3"5 Following installation, the GR systems
were tested over a range of conditions and the operators were trained to achieve an optimum
balance of NOX control and boiler performance in normal commercial service. EER
monitored performance over these long term testing periods. Previous papers have presented
the SO2 control results6'7 and interim data from the three field evaluations.8"17 This paper
presents the final NOX control results and compares the performance achieved at the three
units.
The Gas Reburning Process
The use of hydrocarbon fuels to reduce NOX emissions has been recognized for some tune.18
In 1972, Dr. lost Wendt coined the term "Reburning" to describe the process.19 In the early
1980s, the Japanese presented extensive pilot scale reburning data and initial demonstration
work.20"21 Subsequently, EER built a US reburning data base22'23 and this work evolved into
the three full scale evaluations discussed in this paper.
With GR, the combustion process is divided into three zones as illustrated in Figure 1. In
the primary zone, the main fuel (which can be coal, oil or gas) is fired through conventional
burners but at a reduced rate to compensate for natural gas which is injected downstream. In
the reburning zone, the gas injection consumes the excess air from the primary zone
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producing a slightly fuel rich region where NOx is reduced by reactions with hydrocarbon
radicals. Overture air is added in the final burnout zone to complete the combustion and to
adjust the overall excess air. Thus, except for relatively minor changes in boiler efficiency,
the total heat input to the furnace is the same as baseline but divided into two streams.
Similarly, the total air supplied to the furnace remains essentially unchanged but is divided
into two streams which supply the conventional burners and the overfire air ports.
In addition to the NOX reduction due to chemical reduction in the reburning zone, additional
NOX reduction occurs due to operation of the primary combustion zone at reduced firing rate
and excess air.
Figure 2 shows how GR can be applied to a front wall fired boiler schematically. No
physical changes to the main burners are required. The burners are simply turned down and
operated with the lowest excess air commensurate with acceptable lower furnace performance
considering such factors as flame stability, carbon loss, and ash deposition. The burner
turndown has several ancillary benefits. First, it provides incremental NC^ reduction as
mentioned above; second, the reduced combustion intensity may lessen ash deposition and
waterwall wastage in the lower furnace; and third, the pulverized coal fineness tends to
improve at turndown conditions which may have a positive impact on carbon loss and/or
excess air level at a given burner throughput.
The natural gas is injected above the main burners through wall ports to produce a slightly
fuel rich reburning zone. Maximum NOX reduction occurs when the reburning zone operates
at about 90% theoretical air (TA).22'23 To achieve this design point with rninimum natural
gas, EER's GR design utilizes gas injectors rather than burners, (which would introduce
additional air).
The air required to burnout the combustibles hi the reburning zone is injected through overfire
air ports positioned above the reburning zone. These ports are similar to conventional
overfire air ports except that they are positioned higher in the furnace so as to maximize the
residence time available in the reburning zone.
Gas Reburning Design Considerations
Due to the substantial design differences among existing boilers and furnaces, GR must be
custom designed to match site specific factors. FJER's GR design methodology utilizes both
analytical and physical models to design the optimum configuration based on site specific
factors and to project performance.5 This section presents an overview of some of the factors
influencing the design including:
• Firing configuration
• Main and reburning fuel characteristics
• Furnace volume
• Gas injector design
• Overfire air design
• Flame sensing and controls
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Firing Configuration
Because GR does not require modifications to the main combustion system, it can be applied
to furnaces with virtually any firing configuration. This paper presents results for applications
to wall, tangential, and cyclone fired systems. There is also potential for application to
stokers and a range of industrial process furnaces. For example, HER is currently developing
GR for application to glass furnaces and a full scale demonstration is planned.24' 25
Main and Rebuming Fuel Characteristics
Since GR involves no physical changes to the main combustion system, it can be applied to
furnaces fired with any fuel (coal, oil, gas, etc.).22'23 The GR installations discussed here
involved both coal and gas as the primary fuel.
Reburning can be accomplished using any hydrocarbon fuel. On purely a performance basis,
natural gas is the preferred reburning fuel offering the following advantages:
1. Natural gas has no ash Thus, fly ash and bottom ash are reduced in proportion to the
amount of natural gas fired.
2. Natural gas has no sulfur Therefore, SQ emissions are reduced in proportion to the
amount of natural gas fired.
3. Natural gas has no bound nitrogen In the reburning zone, a portion of the bound nitrogen
may be converted to NOX countering the chemical reduction via reburning. This is
especially important for reburning applications where the baseline NOx is low and the
desired control is deep.
4. Natural gas is 100% volatiles No fuel preparation (such as pulverization or atomization)
is required thus reducing the capital cost of the GR installation. With gas, all of the
hydrocarbons are immediately available for reaction maximizing the time available for
the NOX reduction process; also, gas has no fixed carbon which requires oxidation in the
burnout region.
Furnace Volume
There must be sufficient space above the burners or cyclones to install the GR components.
By designing the reburn fuel and overfire air injectors for rapid mixing, space requirements
are in the range typically available on full scale utility boilers. EER has designed GR
systems for numerous boilers and has yet to find a commercial system where the residence
time was inadequate. In the cyclone GR retrofit discussed here, the residence time in the
reburning zone was only 0.25 seconds. Nevertheless, NOX reduction in excess of 70% was
achieved. Nevertheless, longer residence times are desirable to minimize the amount of gas
required to achieve a specific NOX control goal.
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Gas Injector Design
Since the NOX reduction reactions are kinetically limited, NOX control is enhanced by
injection at high temperatures. Thus the gas injector should be located close to the upper
firing elevation but leaving enough space to achieve essentially complete combustion prior to
gas injection.
For maximum NOX reduction, the natural gas must be injected so as to penetrate across the
furnace width and rapidly mix with the furnace gases. Since the amount of gas injected is
small compared to the furnace gas flowrate, achieving penetration and rapid mixing is a
challenge, especially on larger sized units. EER uses a combination of analytical and physical
modeling to evaluate alternate injection configurations and identify optimum configurations.
There are two approaches to enhancing mixing: increasing the flowrate of the injected
material via flue gas recirculation (FOR) and the use of high velocity gas jets. The three GR
systems discussed here all use FOR. One system was subsequently modified to eliminate
FOR.
Overfire Air Design
Since the main combustion zone operates with excess air and most of the char oxidation is
completed there, the principal function of the overfire air is to burnout the CO and gaseous
hydrocarbons exiting the reburning zone. The overfire air ports should be located high in the
furnace so as to maximize reburning zone residence time. However, the mixing and final
oxidation should be completed prior to the convective pass. As with the gas injectors, the
overfire air ports need to be designed so as to obtain rapid and complete mixing.
Flame Sensing and Controls
EER integrates the GR system with the normal boiler controls for fully automated operation.
Depending on the NOX control goals, the gas injection can be fixed or varied in response to
boiler operating conditions and/or NOX emissions. The gas injection controls include both
permissive and trips which ensure safe operation. Since the gas injection does not produce a
visible flame, conventional scanners are ineffective. Instead, furnace temperature is used as a
permissive/trip. This approach has been fully effective in the three GR installations and has
been reviewed and approved by both Factory Mutual and Hartford Steam on the three field
installations.
Gas Reburning Designs and NO* Control Performance For Three Utility Boilers
GR was applied to three coal fired utility boilers as shown in Table 1. The site specific GR
designs and NOX control performance are discussed in the subsections below.
Tangentially Fired Unit, Illinois Power Hennepin 1
Illinois Power's Hennepin Station is located on the Illinois river about 100 miles southwest of
Chicago. Unit 1 has a capacity of 71 MW net. The Unit 1 boiler is tangentially fired with
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three burner elevations. It normally fires Illinois bituminous coal but is also equipped to fire
up to 100% natural gas.
EER designed an integrated GR-Sorbent Injection (SI) system for the Hennepin unit. The GR
system was designed to operate with or without the SI system in operation and is illustrated
in figure 3. The Hennepin furnace has a relatively large space between the upper row of
burners and the furnace nose. This allowed the GR system to be designed with a generous
reburning zone residence time of 0.55 seconds. The reburning fuel was injected along with
FGR through tilting nozzles on the furnace walls near the corners at the top of the windbox.
During the optimization tests, tilt was found to have little impact on performance. The
overfire air ports were located on the furnace walls near the corners below the nose.
Baseline NOX emissions were 0.75 lb/106 Btu. In parametric optimization tests, Gas
reburning reduced NOX emissions by 75 % to 0.19 lb/106 Btu. Following optimization tests,
the plant operators operated the GR system in normal commercial service which involved
daily cycling. Figure 4 shows the NOX emissions measured during the long term tests. The
average emissions were 0.245 lb/106 Btu, a 67% reduction from baseline.
Cyclone Fired Unit, City Water, Light and Power Lakeside 7
City Water, Light and Power's Lakeside Station is located on Lake Springfield hi Springfield
Illinois. Unit 7 is a 33 MW net cyclone fired unit which normally fires an Illinois bituminous
coal. There are two cyclones discharging into a secondary furnace of the "well"
configuration. As with the Hennepin unit, EER designed an integrated GR-SI system for the
Lakeside unit which could be operated with or without the SI system in operation.
Figure 5 shows how the GR components were integrated into the Lakeside furnace. This GR
application was the most challenging of the three and illustrates the potential to configure GR
to complex situations. The two counter-rotating cyclones discharge into a refractory lined
well. Within the well, the combustion products transition into a jet moving up the rear wall.
This high velocity region and the divergence of the furnace walls produce a large
recirculation zone extending across most of the furnace. As a result, the available residence
time in the reburning zone is limited to 0.25 seconds.
The gas and FGR injectors were located along the rear wall and side walls at the top of the
refractory well. Although the penetration distance was short, fast mixing was required due to
the limited reburning zone residence tune. Overfire air was injected from the rear wall in the
upper furnace. This also posed a challenge since any overfire air which penetrated through to
the recirculation zone could be transported down to the reburning zone.
Baseline NOX emissions were 0.95 lb/106 Btu. In parametric optimization tests, GR reduced
NOX emissions by 74 % to 0.26 lb/106 Btu. Following optimization tests, the plant operators
operated the GR system in normal commercial service. This unit typically operates as a
peaker during winter and summer months. Figure 6 shows the NOx emissions measured
during the long term tests. The average emissions were 0.344 lb/106 Btu, a 66% reduction
from baseline.
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Wall Fired Unit, Public Service Company of Colorado Cherokee 3
Public Service Company of Colorado's Cherokee Station is located near Denver, Colorado.
Unit 3 has a capacity of 158 MW net and is front wall fired with 16 burners in a 4 x 4 array.
The retrofit involved integration of Foster Wheeler commercial low NOx burners with GR.
The GR system was designed based on the baseline performance of the unit and the projected
performance of the Foster Wheeler burners. Figure 7 shows how the GR components were
integrated into the Cherokee furnace. The reburning fuel was injected with FGR through
ports on the front and rear furnace walls above the top burner row. Overfire air was injected
through ports on the front wall only just below the nose. This configuration provided a
reburning zone residence time of 0.5 seconds. This initial configuration was tested and then
subsequently modified as discussed in a subsequent section below.
Baseline NOX emissions were 0.73 lb/106 Btu. The low NOX burners (initial design) reduced
NOX by 35 % to 0.48 lb/106 Btu. In optimization tests, operation of the initial GR design in
conjunction with the low NOX burners achieved 72% reduction to 0.20 lb/106 Btu. Figure 8
shows the NOX emissions measured during the long term tests. The average emissions were
0.26 lb/106 Btu, a 64% reduction from baseline.
Gas Reburning with Gas as the Main Fuel
Two of the units, Hennepin 1 and Cherokee 3 were equipped to fire natural gas through the
main burners. This provided an opportunity to evaluate GR using gas as the main fuel. Tests
were conducted at full load firing 100% gas entirely through the main burners and in the GR
mode. Figure 9 shows the results from both units. Switching from 100 % coal to 100 % gas
without GR reduced NOX to 0.14 and 0.32 lb/106 Btu for Hennepin and Cherokee
respectively. GR operation reduced NOX emissions by an additional 56 and 64 % percent,
respectively. Minimum NOX emissions were 0.14 and 0.05 lb/106 Btu which correspond to
total reductions of 81 and 93 % from the uncontrolled baseline.
Comparing NOX Control Performance
Figure 10 compares the NOX emissons for the three GR installations as a function of the
reburning gas heat input percentage. For all three, NOx decreases as the reburning gas heat
input increases. For the tangential and wall fired units, the slope of the curve is relatively flat
over the reburning gas heat input range of 10-20 % while for the cyclone unit (with shorter
reburning zone residence time, NOX continues to decline as the reburning gas heat input is
increased over this range.
Figure 11 compares the results for the three GR installations using a different perspective to
illustrate the wide range of conditions evaluated and the similarity in GR NC^ control for all
these conditions. NOX emissions (lb/106 Btu) are plotted as a function of the NOX reduction
(%). Each line represents the full range of possible NOx control for the specific unit.
Baseline emissions correspond to zero % NC^ reduction and for 100 % NOX reduction the
NOX emissions are zero lb/106 Btu by definition. The maximum short term NC^ reduction
and average long term NOX reduction for each unit are shown as points along the lines
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including data for both gas and coal as the main boiler fuels. Except for the Cherokee unit,
which is a special case due to the integration with Low NO* burners, the results are
consistently in the range of 60 to over 70% reduction regardless of baseline NO^ (over nearly
an order of magnitude range), primary fuel (coal or gas), or firing configuration.
Performance and Durability Impacts
In addition to the NOX data, the field evaluations included comprehensive measurements of
boiler performance and durability impacts. The effects on emissions other than NC^, boiler
thermal performance, ash deposition and durability are summarized below.
Emissions Other Than NOX
As with other combustion modification emission controls, CO emissions from GR depend on
overall excess air (after overfire air addition). For excess air comparable to normal
uncontrolled operation, CO emissions were close to baseline.
Since gas contains no sulfur, GR reduces SO2 emissions in direct proportion to the gas firing
rate. Additional SO2 reduction was achieved at Hennepin and Lakeside via Sorbent Injection.
Thermal Performance
GR produces subtle changes in boiler thermal performance. The primary factors are:
1. The H/C ratio of natural gas is higher than coal.
2. The heat release distribution in the furnace is shifted upward.
3. The residence time of combustion products in the lower furnace is increased due to the
lower burner or cyclone firing rate.
4. The GR system can be tuned to achieve carbon hi ash and CO emissions comparable to
baseline values and well within commercial guarantee requirements.
The net effect of all of these factors is typically a slight reduction in boiler efficiency. Over
the long term testing periods, the boiler efficiency reductions for the three GR systems ranged
from 0.5 to 1.7%. For ah1 three Installations GR decreased furnace heat absorption slightly
and this translated into an increase in superheat attemperation at full load. The increase was
within the capacity of the existing attemperation flowrate; no modifications were required.
Ash Deposition
GR lowers the combustion intensity in the lower furnace. Therefore, a unit experiencing ash
deposition in this area under baseline operation might benefit from GR. In these units, there
were no ash deposition problems in the lower furnace under normal operation or with GR.
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The ash fusion temperatures for most coals (including those tested here) are lower under
reducing conditions. This suggests that the slightly fuel rich conditions in the reburning zone
could increase ash deposition. During the tests of all three units, some sporadic ash deposits
were observed around the reburn fuel injectors. They were similar to eyebrows and extended
a few inches into the furnace. These deposits were not considered significant by the operators
and did not appear to affect GR operation or furnace performance. In future GR installations,
EER intends to install wall blowers near the reburn injectors for additional ash deposition
control.
Durability
The reburning zone operates at slightly fuel rich conditions. This suggests the possibility of
increased tube wastage due to removal of the protective oxide layer and/or sulfide attack.
Accordingly, the field evaluations included a comprehensive program of both destructive and
non-destructive (ultrasonic tube thickness - UT) evaluations. Data from the Hennepin and
Lakeside have been evaluated and there is no evidence of increased tube wastage attributable
to GR.
Second Generation Gas Reburning
The three GR systems all used FGR to enhance the penetration and mixing of the reburning
gas. While high velocity gas jets could have been used instead of FGR, FGR was selected as
the more conservative approach for these initial demonstrations since the penetration and
mixing are controlled by the FGR flowrate essentially independent of the natural gas flowrate.
However, FGR adds substantially to the capital cost of the GR system and also contributes
slightly to the increased superheat attemperation rate.
Following the initial tests of the Cherokee unit, modifications were made to the low NOx
burners as well as the GR system. The GR modifications included:
1. Replacement of the FGR assisted gas injectors with high velocity injectors without FGR
2. Replacement of the single passage overfire air ports with dual concentric ports to provide
improved control at the low overfire air flowrates associated with reduced gas injection
rates.
Figure 12 compares the NOX emissons from the initial and modified systems. The low
burner modifications reduced NOX marginally. The GR modifications had no impact on NOX.
Since the second generation system reduces capital cost substantially, EER intends to use this
simplified design on all future GR installations where applicable.
Cost Considerations
GR must be integrated with existing power plant equipment. Therefore, the capital costs
depend on site specific factor such as unit capacity, primary fuel type, firing configuration,
geometry of the upper furnace, space availability, type of controls, presence of asbestos,
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windbox/furnace pressure differential, and availability of gas on site. For large units
(nominally 300 MW) where gas is available on site, EER estimates that the capital cost of a
second generation GR system will be in the range of 15 $/kw.
Except for the differential fuel costs and the (previously discussed) impact of the higher
hydrogen content of the fuel on unit efficiency, the operating costs of GR are small. None of
the components are subject to unusually severe operating conditions and there are no
significant maintenance requirements. The GR system is controlled from the control room;
no additional operator labor is required. On coal fired operations, the reduction in coal firing
rate produces a commensurate reduction in coal related O&M costs such as ash disposal,
pulverizer maintenance, and convective pass erosion. There may also be an associated
improvement in availability.
For GR applications to gas fired units, injecting gas in the reburning zone instead of through
the burners has no operational cost impact. However, for other primary fuel, natural gas may
cost more than the fuel it replaces on a heating value basis. This is the principal operating
cost for coal fired boilers. Of course, a portion of the gas-coal cost differential is offset by
the value of the reduction in SO2.
At most plants, natural gas can be supplied via a short connection to a local gas distribution
network or an interstate pipeline. A range of contracting arrangements can be employed
including financing the pipeline via a gas purchase or transport agreement. EER can assist in
evaluating these alternatives.
Conclusions
In conclusion, GR has been successfully applied to three utility boilers of tangential, wall and
cyclone firing configuration covering the range of 33 to 158 MW net. On all three units, GR
was operated with the boilers firing coal. On two of the units, additional tests were
conducted with the boilers operating on gas. On one unit, GR was integrated with
conventional low NOX burners. In all cases NOx reductions exceeded 60% and maximum
reductions of up to 75% were achieved. There were no significant operational or durability
problems.
The results of these three field evaluations have validated EER's design methodology.
Accordingly, EER is now offering GR as a commercial NOx control technology with
emissions control and performance guarantees.
Acknowledgments
These field evaluations of GR would not have been possible without the financial support and
cooperation of several organizations. The work at all three sites was conducted under the
DOE Clean Coal Technology Program through DOE Cooperative Agreement No. DE-FC22-
87PC79796 and DE-FC22-90PC90547. The Gas Research Institute provided cofunding for all
three sites via Contract No. 5087-254-149 and 5090-254-1994 and . The State of Illinois
Department of Energy and Natural Resources provided cofunding for the Hennepin and
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Lakeside sites. The Electric Power Research Institute provided cofunding for the Cherokee
site under Cost Sharing Agreement RP2916-23. Colorado Interstate Gas provided cofunding
for the Cherokee site. The three host utilities, Illinois Power, City Water, Light and Power,
and Public Service Company of Colorado, provided access to the host units and in kind cost
sharing. The authors wish to express their appreciation to the operating staff of Hennepin,
Lakeside and Cherokee Stations.
References
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Table 1
Characteristics of the Three Host Boilers Retrofitted with Gas Reburning
Utility
Illinois Power
City Water, Light
and Power
P.S. Colorado
Station
Unit
Capacity (MW net)
Firing Configuration
Primary Fuel
Secondary Fuel
Baseline NOX
lb/106 Btu
ppm @ 3% O2
Emission Controls
Gas Reburning
Sorbent Injection
Low NOV Burners
Hennepin
1
71
Tangential
Illinois Bit. Coal
Natural Gas
0.75
550
X
X
Lakeside
7
33
Cyclone
Illinois Bit. Coal
None
0.95
695
X
X
Cherokee
3
158
Front Wall
Colorado Bit. Coal
Natural Gas
0.73
535
X
X
-------
c
PRIMARY
ZONE
Low Excess Air
t
INOX -90%
C
REBURNING
ZONE
)
Slightly Fuel Rich
^^^•^^
Gas
C
BURNOUT
ZONE
)
Normal Excess Air
Figure 1
The Gas Reburning Process
Coal
82%
Zone
Burnout
Reburning
Main
Combustion
Conditions
Normal
Excess Air
Slightly
Fuel Rich
Low
Excess Air
NOY Reduction
A.
No
Change
HxCY
Reactions
Reduced Load
Reduced Excess Air
Figure 2
Typical Gas Reburning Installation on a Wall Fired Boiler
-------
Figure 3
Gas Reburning Applied to Hennepin Unit 1
NOX
(lb/106 Btu)
1
0.9-
0.8-
0.7-
0.6-
0.5-
0.4-
0.3-
0.2-
0.1-
0-
Baseline NOX= 0.75 lb/106 Btu
Average GR NOX= 0.245 lb/106 Btu
o
January 10, 1992 to October 19, 1992 (75 data points)
Figure 4
Long Term NCL Emissions for Gas Reburning on Hennepin 1
-------
NOX
(lb/106 Btu)
Figure 5
Gas Reburning Applied to Lakeside Unit 7
1-
0.9-
0.8-
0.7-
0.6-
0.
0.1-
0-
Baseline NOX= 0.95 lb/106 Btu
Average GR NO = 0.344 lb/106 Btu
October 5,1993 to June 2, 1994 (123 data points)
Figure 6
Long Term NOX Emissions for Gas Reburning on Lakeside Unit 7
-------
NOX
(lb/106Btu)
0.9
0.8-
0.7-
0.6
0.5-
0.1-
0-
Reburn
Fuel
Over Fire
Air
Reburn
Fuel
Primary
Burner
Zone
(LNBs)
Figure 7
Gas Reburning Applied to Cherokee Unit 3
Baseline NOX= 0.73 lb/106 Btu
o Average GR NOX = 0.260 lb/106 Btu
April 27,1993 to June 10,1994 (214 data points)
Figure 8
Long Term NOX Emissions for Gas Reburning and Low NOX Burners on Cherokee Unit 3
-------
NOX
Ob/106 Btu)
0.35-
0.3-
0.25-
0.2-
0.15
0.1
0.05
0-
Cherokee
(GR)
Hennepin
(GR)
Cherokee
(Baseline)
Hennepin
(Baseline)
0.8
0.9 1 1.1
Reburning Zone Stoichiometry
1.2
1.3
Figure 9
Gas Reburning With Gas as the Primary Fuel on Lakeside Unit 7 and Cherokee Unit 3
NOX
(lb/106Btu)
10 15 20
Natural Gas Injection (%)
Figure 10
Gas Reburning NOX Reduction as a Function of Gas Injection Rate
-------
NOX
Ob/106 Btu)
1
0.9
0.8
0.7
0.6
0.5
0.4
0.3
0.2
0.1
0
Lakeside
(cyclone)
Hennepin
(tangential)
0 10 20 30 40 50 60 70 80
NOX Reduction (%)
Figure 11
Comparison of Gas Reburning NOX Control Performance
90 100
NOX
ab/106 Btu)
2.5
3.5 4 4.5
Excess O2 (%)
• Baseline
• LNB
A GR-LNB
O LNB-mod
A GR-LNB Mod
Figure 12
Comparison of First and Second Generation Gas Reburning on Cherokee Unit 3
-------
Gas Reburn Retrofit on an Industrial Cyclone Boiler
H. Farzan, C. E. Latham, G. J. Maringo, and J. E. Hallstrom
Babcock & Wilcox
C. T. Beard and G. E. Weed
Eastman Kodak Company
John Pratapas
Gas Research Institute
Submitted for Presentation at the
EPRI/EPA 1995 Joint Symposium on Stationary Combustion NOX Control
Abstract
Eastman Kodak Company's cyclone boiler (Unit No. 43), located in Rochester, New York, is be-
ing retrofitted with the gas reburning technology developed by Babcock & Wilcox (B&W) to re-
duce NOX emissions in order to comply with the Title I, ozone nonattainment, of the Clean Air
Act Amendments (CAAA) of 1990. The required NOX reduction from baseline levels necessary
to meet the presumptive limit set in New York's regulation is about 47%.
Eastman Kodak and the Gas Research Institute (GRI) are cosponsoring this project. B&W is the
prime contractor and contract negotiations with Chevron as the gas supplier are presently being
finalized. Equipment installation for the gas reburn system is scheduled for a September 1995
outage.
No. 43 Boiler's maximum continuous rating (MCR) is 550,000 pounds per hour of steam flow
(or approximately equivalent to 60 MWe). Because of the compact boiler design, there is insuffi-
cient gas residence time to use pulverized coal or oil as the reburn fuel, thus making it a prime
candidate for gas rebum. Kodak currently has four cyclone boilers. Based on successful comple-
tion of this gas reburn project, modifying the other three cyclone boilers with gas reburn technol-
ogy is anticipated.
The paper will describe B&W's gas reburn data from a cyclone-equipped pilot facility (B&W's
Small Boiler Simulator), gas reburn design information specific to Eastman Kodak No. 43 Boiler,
and numerical modeling experiences based on the pilot-scale Small Boiler Simulator (SBS) re-
sults along with those from a full-scale commercial boiler.
-------
Introduction
The Clean Air Act Amendments of 1990 pose significant challenges to electric utilities to reduce
both sulfur dioxide (SO^) and oxides of nitrogen (NOX) emissions. The Act mandates an ap-
proximate 3.5 million ton-per-year reduction in SO2 emissions from 111 selected existing utility
boilers by January 1, 1995. An additional 5.3 million ton-per-year reduction is also mandated to
occur by January 1, 2000, in order to reach a long-term SO2 emissions cap of 8.9 million tons per
year. Titles I and IV of the Act mandate NOX reduction from stationary sources. Title IV (acid
rain) requires the use of low-NOx burner technology and Title I (ozone nonattainment) requires
RACT (reasonable, available control technology) to reduce NOX. The impact on utilities is that
by the year 2000, more than 200,000 MWe of electricity generating capacity must be retrofitted
with low-NOx systems.
The limitations imposed by the act are particularly challenging, especially for NOX emissions to
cyclone-fired boilers. The cyclone furnace consists of a cyclone burner connected to a horizontal
water-cooled cylinder — the cyclone barrel. Air and crushed coal are introduced through the cy-
clone burner into the cyclone barrel. The larger coal particles are thrust out to the barrel walls by
the cyclonic motion of combustion air where they are captured and burned in the molten slag
layer that is formed; the finer particles burn in suspension. The mineral matter melts and exits
the cyclone via a tap at the cyclone throat that leads to a water-filled slag tank. The combustion
gases and remaining ash leave the cyclone and enter the main furnace.
Typical low-NOx burners and staged combustion techniques are not applicable to cyclones be-
cause these techniques rely on developing an oxygen deficient or reducing atmosphere to hamper
NOX formation. A reducing condition in the confines of a cyclone barrel is unacceptable due to
the potential for tube corrosion and severe maintenance problems which result. Cyclone opera-
tion must occur with excess oxygen in the cyclone barrel, and this condition coupled with high
temperatures and severe turbulence within the cyclone barrel is the reason why cyclones are dis-
proportionately high generators of NOX.
The emerging reburning technology offers cyclone boiler owners a promising alternative to ex-
pensive flue gas cleanup techniques for NOX emission reduction. Reburning involves the injec-
tion of a supplemental fuel (natural gas, oil, or coal) into the main furnace in order to produce
locally reducing conditions which convert NOX produced in the main combustion zone to mo-
lecular nitrogen, thereby reducing overall NOX emissions.
Cyclone-fired boilers represent approximately 26,000 MWe of generating capacity in the U.S.,
which is approximately 15% of pre-New Source Performance Standards (NSPS) coal-fired gen-
erating capacity. These units contribute about 21% of NOX emitted by pre-NSPS coal-fired units.
The Eastman Kodak Company has four coal-burning cyclone boilers at their Rochester, New
York, facilities. These boilers are subject to Title I compliance (ozone nonattainment). To com-
ply with New York State requirements, Kodak requested that B&W perform an engineering feasi-
bility study to determine the best RACT. B&W concluded that due to compact boiler design, gas
rebum technology is the most viable for these boilers. Since Kodak's boilers are relatively small,
-------
the average furnace residence time is less than that available in larger cyclone units. Thus, coal or
oil reburn technologies are not feasible in Kodak's boilers. The final step to determine RACT is
to demonstrate the gas rebum technology in one of these boilers (No. 43 Boiler) in order to deter-
mine specific NOX reduction potential and cost of NOX control for boilers designed with mini-
mum available furnace resident times.
The current uncontrolled NOX level in No. 43 Boiler is 1.37 Ib/MBtu at peak load. The required
NOX reduction from this baseline level necessary to meet the presumptive limit set by the New
York State regulation is about 47%. Based on successful completion of this gas reburn project,
modification of the other three cyclone boilers with gas reburn technology is anticipated.
Background/Reburning Process Description
To address the special needs of the cyclone boiler population with respect to NOX reduction,
B&W pursued the reburning technology. The reburn technology development for cyclone boilers
was performed via: 1) an initial engineering feasibility study (funded by EPRI Project RP-1402-
30), 2) a pilot-scale evaluation co-funded by Electric Power Research Institute (EPRI RP-2154-
11) and the Gas Research Institute (GRI 5087-254-1471), and B&W, and 3) a U.S. Department of
Energy's Innovative Clean Coal Technology demonstration at Wisconsin Power and Light's
Nelson Dewey station.1'4
The feasibility study suggested that the majority of cyclone-equipped boilers could potentially
apply this technology in order to reduce NOX emission levels by as much as 50-70%.x The major
criterion that substantiated this potential was that of sufficient furnace residence time which does
exist within these boilers, allowing application of the technology. This residence time is required
for both the NOX reduction process in the reburn zone and subsequent combustion completion in
the burnout zone to occur within the boiler. Based upon this conclusion, the next level of confir-
mation, pilot-scale evaluation, was justified. The pilot-scale tests evaluated the potential of natu-
ral gas, oil, and coal as the reburning fuel in reducing NOX emissions.2 The pilot-scale data
confirmed the results of the feasibility study and showed that reburning is technically feasible
and potentially viable technology for cyclone boiler owners. Coal was then selected as the
reburn fuel to be used during the Clean Coal project at Wisconsin Power & Light (WP&L)
Company's Nelson Dewey station. WP&L reburn demonstration validated the results of both the
engineering feasibility and pilot-scale studies results.3'4
Reburning is a process by which NOX produced in the cyclone is reduced (decomposed to mo-
lecular nitrogen) in the main furnace by injection of a secondary fuel. The secondary (or
reburning) fuel creates an oxygen-deficient (reducing) region that accomplishes decomposition of
the NOX. Since reburning is applied while the cyclone operates under normal oxidizing condi-
tions, its effects on cyclone performance can be minimized.
The reburning process employs multiple combustion zones in the furnace, defined as the main
combustion, reburn, and burnout zones as shown in Figure 1. The main combustion zone is op-
erated at a stoichiometry of 1.1 (10% excess air) and combusts the majority of the fuel input (65
to 85% heat input). The balance of fuel (15 to 35%) is introduced above the main combustion
-------
zone (cyclones) in the rebum zone through reburning burners (see Figure 2). These burners are
operated in a similar fashion to a standard wall-fired burner, except that they are fired at ex-
tremely low stoichiometries. The oxygen deficient combustion gases from the reburn burners
mix with combustion products from the cyclones to obtain a furnace reburning zone stoichiom-
etry in the range of 0.85 to 0.95, which is needed to achieve maximum NOX reduction based on
laboratory pilot-scale results. A sufficient furnace residence time within the reburn zone is re-
quired for flue gas mixing and NOX reduction kinetics to occur.
The balance of the required combustion air (totaling 15 to 20% excess air at the economizer out-
let) is introduced through overfire air (OFA) ports. B&W's Dual Air Zone Ports are designed
with adiustable air velocity controls to enable optimization of mixing for complete fuel burnout
prior to exiting the furnace (see Figure 3). As with the reburn zone, a satisfactory residence time
within this burnout zone is required for complete combustion.
OVERFIRE
AIR PORTS
REBURNING..
BURNER
BURNOUT
ZONE
REBURN
ZONE
NO + NH.
=*N2 + ....
3-4% EXCESS 02
0.85 - 0.95
STOICHIOMETRY
CYCLONES
MAIN \
COMBUSTION
ZONE
(_
Figure 1 - Reburning Process
-------
Sliding Air
Damper Drive
Oil
Burner
Adjustable/
Removable
Gas Spuds
Sliding Air Damper
Air Flow
Monitor
j
Furnace
^
Core Air
Adjustable
Sleeve
Adjustable
Spin Vanes
Figure 2 - Reburn Burners
Furnace Wall
Tubes
Manual
Adjustment
Handles
7— r
Sliding Air Air Flow
Damper Monitors
Adjustable
Spin Vane
Overfire Air Windbox
(Depth is site specific)
Figure 3 - Dual Air Zone Overfire Air Port Assembly
-------
Project Description
Project Objectives
The objective of this project at Eastman Kodak Company's No. 43 Boiler is to demonstrate the
long-term application of gas reburning to reduce NOX/SO2 emissions from a coal-fired cyclone
boiler while maintaining acceptable cyclone boiler operating conditions.
Specific objectives of this demonstration project are as follows:
• To maximize NOX emission reduction at peak load. The guaranteed NOX emission rate is a
47.5% NOX reduction from the baseline level of 1.37 Ib/MBtu and is expected to be
achieved while using 28% (or less) natural gas as a percentage of total heat input to the
boiler. Flue gas recirculation (FOR) to the reburn burners is available to provide mixing/
burner stability and flexibility.
• To achieve a SO2 reduction proportional to the gas heat input.
• To demonstrate boiler operational safety and acceptable turndown with reburn.
• Minimal impact on boiler turndown. The current turndown for No. 43 Boiler is 70% of
maximum continuous rating (MCR). At this load, boiler slag tap freezing is initiated. With
the introduction of reburn fuel into the boiler, boiler turndown will be evaluated.
• Minimal impact on combustible losses (less than 0.1 percentage point change in combustion
efficiency).
• CO levels of equal to or less than 200 ppm — B&W anticipates that CO levels will be be-
tween 100 and 150 ppm on a day-to-day operational basis.
• No major impact on boiler tube losses. No. 43 Boiler has not experienced major tube losses
within the main boiler in the past. Reburning is not expected to increase the tube deteriora-
tion. The quantitative objective with reburn in service is to have no adverse impact on cur-
rent expectations to continue to operate No. 43 Boiler over the next 20 years.
• Our goal is to obtain NOX removal at a maximum cost of $2000 per ton of NOX removed.
B&W cost information currently shows that the cost of NOX control ranges between $748
and $1,866 per ton removed. These estimates were developed based on gas/coal price differ-
ential ranging from $0.75 to $2.36 per MBtu, baseline NOX level of 1.37 Ib/MBtu, 28%
natural gas as a percentage of total heat, and a 20-year project life.
• The capital cost of the reburn system should not exceed $75/kW for the small cyclone boil-
ers. The capital cost is high due to the small size of the boiler (economy of scale is not avail-
able here, e.g., at 100 MWe the cost is $16 to $17 per kW without controls). Although the
cost of instrumentation and controls is site-specific, it is included in this estimate.
-------
Project Methodology
B&W's methodology for designing and operation of a reburn system at Eastman Kodak is identi-
cal to that used on the previous full-scale reburn application. This includes using the previously
acquired pilot-scale gas rebum data, baseline characterization of No. 43 Boiler, a site-specific en-
gineering study including scale-up of the results using proprietary B&W numerical models vali-
dated with baseline information, and finally full-scale design, installation, and commercial
operation. Once the system is in operation, a commercial evaluation, including revised cost in-
formation will be developed.
Project Tasks
In order to accomplish the objectives of this project, the following tasks are planned:
Task 1 Finalize agreements
Task 2 - Engineering design
Task 3 - Test plan completion
Task 4 - Equipment fabrication and installation
Task 5 - Field testing
Task 6 - Data interpretation
Task 7 Management and reporting
Project Organization
The project team is as follows:
• Eastman Kodak Company — Host site and co-sponsor
• Gas Research Institute — Co-sponsor
• B&W — Boiler manufacturer and prime contractor
• Chevron U.S.A. — Gas supplier
• Rochester Gas & Electric — Gas distributor
• Acurex — Field monitoring
Project Schedule
A schedule of 18 months is planned for this project, as shown in Figure 4. Equipment installa-
tion for the gas reburn system is scheduled for a September 1995 outage. At the conclusion of
this 18-month project, the reburn system will be optimized and delivered to Kodak for day-to-day
commercial operation from December 1995 through May 1997. The boiler will go though an
outage in June 1997 when the long-term performance of the reburn system and its effect on boiler
tube life will be assessed.
-------
Task Description
1 Finalize Agreement
2 Engineering Design
2-1 Numerical Modeling
3 Test Plan Completion
4 Equipment Fab. & Install.
5 Field Testing
6 Data Interpretation
7 Management & Reporting
1994
S
O I N
J
X
)
D
1995
J
)
F
I
M
A
M
J
J
A
S
^fc_
T
O
—
N
—
U
••
1996
J
h
I
+ 4-Week Planned Outage for Reburn Installation
© Participation Agreement with Kodak
O Interim Update
•& Test Plan
V Final Report
Figure 4 - Project Schedule
Review of Previous Pilot-Scale Experiments
B&W's 6-million Btu/hr small boiler simulator (SBS) was utilized to perform the pilot-scale
study (Figure 5). This pilot-scale facility and the reburn results are described in detail else-
where.2 A short description of the facility pertinent to scale-up is presented here.
Experimental Facility
The SBS is fired by a single, scaled-down version of B&W's cyclone furnace. Coarse pulverized
coal (44% through 200 mesh), carried by primary air, enters tangentially into the burner. Pulver-
ized coal is used in the SBS instead of crushed coal in order to obtain complete combustion in
this small cyclone. Preheated combustion air at 600 to 800 F enters tangentially into the cyclone
furnace.
The water-cooled furnace simulates the geometry of B&W's single-cyclone, front-wall fired cy-
clone boilers. The inside surface of the furnace is insulated to yield typical full-scale furnace exit
gas temperatures (FEGT) at the design heat input rate of 6-million Btu/hr. This facility simulates
fumace/convective pass gas temperature profiles and residence times, NOX levels, cyclone
slagging potential, ash retention within the resulting slag, unburned carbon, and fly ash particle
size of typical full-scale cyclone units. A comparison of baseline conditions of these units is
shown in Table 1.
-------
STEAM
REHEATER
DEPOSITION —
PROBE
SUPERHEATER
FOULING TUBE
DEPOSITION PROBE
REBURNING
BURNERS
FLUE GAS
RECIRCULATION
FURNACE ARCH
PRIMARY AIR
AND COAL
TERTIARY AIR
SECONDARY AIR
SLAG TAP
MOLTEN SLAG
SLAG COLLECTOR
AND FURNACE
WATER SEAL
Figure 5 - Small Boiler Simulator (SBS) Facility
Table 1
COMPARISON OF BASELINE CONDITIONS
FORTHE SBS FACILITY AND COMMERCIAL UNITS
Cyclone Temperature
Residence Time
Furnace Exit Gas Temperature
NOX Level
Ash Retention
Unburned Carbon
Ash Particle Size (MMD; Bahco)
SBS
>3000 F
1.4 seconds*
2265 F
690- 1200ppm
50 - 85%
<1 % in ash
6 - 8 microns
Typical Cyclone Boilers
>3000 F
0.5-2 seconds
2200 - 2350 F
600- 1400ppm
60 - 80%
1 - 20%
6-11 microns
At full load
-------
Two reburning burners are installed on the SBS furnace rear wall above the cyclone furnace.
Each burner consists of two zones, with the outer zone housing a set of spin vanes, while the in-
ner zone contains the reburning fuel injector. Air and flue gas recirculation (FOR) can be intro-
duced through the outer zone. Overfire air (OFA) ports are located on both the front and rear
walls of the SBS at three elevations, with each elevation containing two ports. Two air-cooled
deposition probes and simulated commercial sootblowers are available in the convective section
(simulating secondary superheater and reheater tubes) in order to allow fouling (deposition) stud-
ies to be performed.
Results
A 40-75% NOX reduction (from a baseline NOX level of 925 ppm at full load and 3% stack O2)
was achieved during reburning tests. Figure 6 shows that NOX emissions decreased with decreas-
ing reburning zone stoichiometry or with increasing percent reburn fuel. Varying the amount of
natural gas reburn from 16 to 28% of total heat input, decreased the NOX emissions from 420 to
235 ppm. These NOX emissions, under reburn conditions, correspond to a 55 to 75% reduction
from the baseline NOX level of 925 ppm at full load and 3% stack oxygen. In addition, the
rebum system showed minimal effect on the unburned combustible losses and FEGT.2
D
LLJ
o
111
oc
oc
o
o
E
0.
Q.
600
500
400
300
200
100
0.95
REBURNING ZONE STOICHIOMETRY
0.90
0.85
I
GAS REBURN
WITHOUT FGR
GAS REBURN
WITH 10% FGR
40
60
LU
O
O
ZJ
Q
111
DC
80
16 18 20 22 24 26 28
NATURAL GAS, PERCENT HEAT INPUT
30
100
Figure 6 - Pilot-Scale NOX Levels
-------
Scale-up Considerations
The comparison of the baseline conditions of the SBS and No. 43 Boiler shows that the pilot-
scale facility sufficiently simulates the full-scale conditions. Although the host site coal was not
tested in the SBS, the baseline NOX levels are close; 1.29 Ib/MBtu for the SBS compared to 1.37
Ib/MBtu for No. 43 Boiler. The temperature profiles in the SBS and No. 43 Boiler are generally
in agreement; above 3000 F at the cyclone throat and approximately the same FEGT. Therefore,
the reburn and burnout zone temperatures are similar. The main difference is that the average
furnace residence time for the SBS is substantially greater than that available for No. 43 Boiler.
Due to this major difference, the results from the SBS are not directly applicable to No. 43
Boiler. The use of numerical modeling along with B&W's empirical NOX curves are thus re-
quired for scale-up of the gas reburn results from the SBS to No. 43 Boiler.
Host Boiler Description and Conceptual Design of the Reburn System
Eastman Kodak's No. 43 Boiler was purchased from Babcock & Wilcox (B&W) in 1968. The
unit is a two-drum Stirling Power Boiler designed for a maximum continuous rating (MCR) of
550,000 Ib/hr steam flow with a four-hour peak rating of 605,000 Ib/hr steam flow. The boiler is
designed with two B&W nine-foot-diameter cyclone furnaces equipped with B&W radial burn-
ers. The cyclones are capable of firing either bituminous coal or heavy fuel oil. Operating steam
pressure and temperature at full load are 1425 psig and 900 F, respectively, at the superheater out-
let with a feedwater temperature of 400 F. The unit is also capable of 450,000 Ib/hr steam flow, while
maintaining full load steam pressures and temperatures at a feedwater temperature of 238 F.
No. 43 Boiler is equipped with a two-stage superheater with interstage attemperation; a horizon-
tal, bare tube economizer; and both a tubular and steam coil air heater. The primary superheater
is located directly in front of the generating bank section and the secondary superheater is in front
of the primary at the furnace outlet. Cyclone riser tubes and wingwalls are also located within
the furnace envelope. Figure 7 shows the original boiler sectional side view.
B&W's reburning technology involves customizing the design to each specific site application in
order to optimize performance. Depending on the boiler design and capacity, B&W evaluates the
effectiveness of using natural gas, oil, or pulverized coal as the reburning fuel. One of the key
parameters in this determination is defined as the available furnace residence time criteria.
Smaller capacity boilers (less than about 650,000 Ib/hr steam flow) typically have minimal fur-
nace residence time and this dictates the use of natural gas reburning. Cyclone boilers of this
size contain either one or two cyclone furnaces and make up approximately 18% of all cyclone
firing capacity.
Eastman Kodak's No. 43 Boiler is one of these uniquely designed cyclone units. As is typical of
the smaller size cyclone units, No. 43 Boiler contains heat transfer surface sections routed verti-
cally up through the furnace region. These sections include the cyclone riser and wingwall tubes.
This feature not only helps minimize furnace residence time, but it also creates reburning design
problems with respect to space limitations for physically locating reburn system components and
in-furnace mixing obstructions.
-------
GAS OUTLET STEAM COIL
"AIR HEATER
Figure 7 - Eastman Kodak Company's Boiler No. 43
-------
The major components of the B&W gas reburn system includes new reburn burners, overfire air
(OFA) ports, ducts and flues to transport air and gas recirculation to the new system components,
air monitors and dampers to control the flow rates, a gas recirculation fan, and controls. B&W S-
type burners are used in the reburn system to provide a stable flame and good mixing characteris-
tics. The burner is operated in a similar fashion to standard wall-fired burner applications (e.g.,
includes a standard flame scanner and gas lighter). Although optional, the reburn system at No.
43 Boiler includes gas recirculation to the burner to maintain maximum mixing flexibility within
the reburn system and thus maximum NOX reduction potential.
Identification of the optimum number, size, and location of the reburn burners and OFA ports is a
critical reburn system design issue. Since the burners and OFA ports require boiler pressure part
openings, physical space limitations are a potential constraint. Basically, two reburn burner loca-
tion options are feasible at No. 43 Boiler (see Figure 8): 1) above the furnace stud line on the
rear wall, or 2) above the furnace stud line on the side walls. Numerical modeling was then used
to evaluate the best burner arrangement based on the resultant mixing effectiveness between the
flue gas from the cyclones and the reburn burner flow.
The major negative aspect of Option 1 — locating the burners on the rear wall — is that the
boiler wingwall header is horizontally located at the approximate desired reburn burner elevation.
Although not improbable to relocate, the cost impact would be substantial. The numerical mod-
eling results (which are discussed later) showed that no benefit is observed when the rear wall ar-
rangement is used.
Numerical Modeling
Mathematical modeling provides the means to scale rebuming technology from pilot-scale fur-
naces to full-scale industrial and utility boilers. The models can be used to adapt the reburning
system to the unique geometry and flow characteristics of a specific boiler. The reburning sys-
tem can alter the furnace flow, combustion, and heat transfer; and the model predictions are used
to determine that these performance changes are within acceptable levels. The models are also
used to optimize the mixing in the reburning and burnout zones.
Mathematical models were used to determine the furnace flow patterns. Figure 9 shows the ve-
locity profiles at the rebum burner elevation. Most of the flow in the furnace passes up along the
side walls. The reburn burners must penetrate and mix with these high velocity regions that con-
tain most of the flow in the furnace.
During the engineering feasibility study, the models were used to evaluate two reburn burner ar-
rangements. The criterion for the evaluation was the maximum percentage of mass flow that
reached substoichiometric conditions in the reburning zone. Nearly the same amount of
substoichiometric flow in the reburning zone was predicted for one reburn burner on each side
wall (two total) and for three burners on the rear wall. Due to the substantial costs for relocating
the wingwall header to accommodate the rear-wall burners, the side-wall burner arrangement was
selected. Subsequently, several cases were run to improve the mixing in the burnout zone. The
objective was to ensure that all of the flow reached stoichiometric conditions at the furnace exit.
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Options for positioning the overfire air ports are limited by the wingwalls and riser tubes. The
four overfire air ports are spaced evenly across the front wall, but the air velocities and flow rates
are higher for the outer two ports. The modeling allowed the overfire air system design to be
matched to the flow from the reburning zone within the limitations of the furnace geometry. The
baseline and optimum reburn flow patterns are shown in Figure 10.
r-H r-l r-J
elev 295' - 2"
elev. 282' - 6"
r*K
OFA Ports
REAR WALL BURNERS
Gas Burners
Case 2
Cyclones
iirtrt
Figure 8 - Alternative Gas Reburn Burner Locations
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Fluid
speed
(ft/s)
Rear wall
I
o
•jo
'tn
i
O5
£
200
175
150
125
100
75
I 50
25
Front wall
Figure 9 - Furnace Gas Flow Distribution Approaching the Reburn Burner
. i r;
'/ t\/fr,
I til n.
i tit,,.
'.'.V1---
BASELINE REBURNING
Figure 10 - Predicted Flow Patterns in Eastman Kodak Boiler No. 43
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While the models can be used to reliably predict the flow, combustion, and heat transfer with
reburning systems, the predictive capabilities for NOX reductions are being benchmarked as part
of this project. Predicted NOX reductions in the SBS are being compared to pilot-scale test re-
sults to benchmark the model. Once the pilot-scale benchmark has been completed, NOX reduc-
tions for No. 43 Boiler will be projected for several operating conditions. These projected
reductions will be compared to field data following start-up. With the validated NOX predictive
capability, the mathematical models provide the comprehensive tools needed for the commercial-
ization of gas reburning technology.
Reburn System Design and Implementations
The gas reburn system is designed to accommodate up to 28% of the total boiler heat input while
operating at 550,000 Ib/hr steam flow. Two B&W S-type reburn burners will be supplied to fire
the natural gas into the boiler and are located one per each sidewall at boiler elevation 282'6"
The burners consist of an inner core zone that houses the natural gas spuds and an outer air zone
that contains adjustable spin vanes. The core zone includes a manual sliding disk to control flow
to this region. In addition to housing the manually adjustable spin vanes, the outer air zone in-
cludes the retractable B&W CFS gas lighter, the scanner sighting ports, and an observation port.
The lighters contain a high energy ignition probe and air cylinders for retracting purposes. The
lighters are to be remotely operated by the Burner Management System or can be operated lo-
cally.
A mixture of secondary air and gas recirculation is introduced to the individual burner windbox.
The air flow source is from the airheater outlet and is controlled/measured via an automatic con-
trol damper and air flow monitor. The gas recirculation source is from the economizer outlet and
a booster fan is available to provide adequate conditions to mix the secondary air with the gas re-
circulation. Isolation dampers and a control damper are available around the fan in order to con-
trol flow, in addition to allowing fan maintenance to be performed while the boiler is operating.
The air and gas recirculation flows will be optimized during start-up activities and control curves
for each of the parameters will be incorporated into the control system.
Four OFA ports will be available to introduce the balance of air flow for complete combustion.
B&W's Dual Air Zone OFA ports will be used to control mixing capabilities from both a pen-
etration and side-to-side mixing standpoint. The OFA ports contain two zones — an inner zone
for penetration versus an outer air zone with manually adjustable spin vanes for side-to-side mix-
ing capability. The ductwork that feeds the air flow to these ports contain control dampers and
air monitors to control and monitor flow rates. Each of the four ports will be contained within
individual windboxes in order to accurately monitor and control flow. As stated with the burner
flow indications, the OFA port flow will be optimized during rebum system start-up and control
curves will be included in the control system.
Future Work
Rebum equipment is being fabricated in B&W's facilities and will be delivered for installation
during an outage scheduled for September 1995. B&W will perform the start-up and shake-
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down activities during the October and November time frame. B&W and Acurex will then per-
form optimization tests. At the conclusion of this 18-month project, the reburn system will be
optimized and Kodak will begin day-to-day commercial operation from December 1995 through
May 1997. The boiler will go through an outage in June 1997 when the long-term performance
of the reburn system and its effect on the boiler tubes will be assessed. With the successful
completion of the project, Kodak will consider the technology for implementation on its other
three cyclone-fired units. B&W believe that the technology will be commercially available fol-
lowing this project.
Acknowledgments
The authors extend their appreciation to Larry Chaney for performing numerical modeling on the
No. 43 Boiler.
References
1. G. J. Maringo, et al., "Feasibility of Reburning for Cyclone Boiler NOX Control," EPA/EPRI
Joint Symposium on Stationary Combustion NOX Control, New Orleans, Louisiana, March 23-
27, 1987.
2. H. Farzan, et al., "Pilot Evaluation of Reburning Cyclone Boiler NOX Control," EPA/EPRI
Joint Symposium on Stationary Combustion NOX Control, San Francisco, California, March 6-9,
1989.
3. H. Farzan, et al., "Reburning Scale-Up Methodology for NOX Control From Cyclone Boil-
ers," International Joint Power Generation Conference, San Diego, California, October 6-10,
1991.
4. A. S. Yagiela, et al., "Update On Coal Reburning Technology for Reducing NOX in Cyclone
Boilers," EPA/EPRI Joint Symposium on Stationary Combustion NOX Control, Washington, DC,
March 25-28,1991.
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LOW NOx PULVERISED FUEL BURNERS
SUMMARY OF PLANT EXPERIENCE
J L King
Babcock Energy Limited
Porterfield Road
Renfrew, PA4 8DJ
SCOTLAND
Abstract
Over the past six years Babcock Energy have retrofitted over 10,000 MW of
electrical" power plant around the world with an advanced pulverised fuel fired
low NOx burner. The burner was developed in 1989 in the Babcock Energy Large
Scale Burner Test Facility in the United Kingdom.
The paper summarises the significant results from the operational experience
gained in the burner retrofits on a wide variety of wall fired boiler
configurations and with a range of fuel g_ualities. Nox reductions of up to
70% have been achieved with no significant adverse effect on boiler efficiency
and with positive operational benefits.
Introduction
The development and first commercial application of an advanced pulverised
coal low NOx burner was presented at the 1991 EPA/EPRI Joint Symposium on
Stationary Combustion NOx Control in Washington D.C. (1). The Low NOx Axial
Swirl Burner has been developed by Babcock Energy Limited (BEL) in response to
increasing environmental pressures in the United Kingdom, retrofit of low NOx
burners to existing utility boiler plant being the electricity generating
companies' preferred initial approach to the reduction of NOx emissions. The
high furnace rating of most U.K. wall fired boilers has resulted in a much
more focused approach to low NOx burner development than may have been applied
elsewhere, the objective being to arrive at a burner design capable of
achieving 650 mg/Nm (6% 0 ) in the retrofit situation i.e. approximately 0.53
Lb/mBtu, with minimum changes to boiler efficiency, carbon in fly ash and CO
levels. A proven efficient low NOx burner is seen as essential to meet future
anticipated NOx emission levels effectively, when combined with other NOx
reduction systems, in terms of additional capital and operating costs.
Design and Development
Low NOx Burner Design Requirements
In a pulverised coal fired utility boiler, inflame NOx reduction is achieved
in the burner zone by burner design, and in particular by ensuring initial
combustion of the fuel in a fuel rich environment. The fuel rich environment
is produced by control of air and fuel mixing within the burner.
Consideration of the results of various fundamental studies on the mechanisms
of NOx formation in pulverised coal flames leads to the following burner
design requirements, (1): -
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1. Maximise the rate of volatile evolution, and total volatile yield, from
the pulverised coal.
2. Provide an initial oxygen deficient zone to minimise NOx formation,but
have sufficient oxygen to ensure flame stability and to maximise the rate
of decay on intermediate nitrogenous species to molecular nitrogen.
3. Optimise both residence time and temperature under fuel rich conditions
in such a way that N formation is maximised.
4. Maximise char residence time under fuel rich conditions to reduce the
potential for the formation of NO from nitrogen retained in the char once
devolatilisation is complete.
5. Add sufficient air and in such a manner that virtually complete fuel
burnout is obtained.
A number of practical considerations are also important:-
1. The low NOx burner should perform in such a way that' the overall
combustion efficiency is not significantly altered.
2. Flame stability and turndown limits should not be impaired.
3. The flame itself should ideally have an overall oxidising envelope to
minimise possible corrosion at the furnace walls.
4. The flame length should be compatible with the furnace dimensions.
Low NOx Axial Swirl Burner Design
Overall Features
Figure 1 shows a typical Low NOx Axial Swirl Burner design. Air staging is
achieved by splitting the combustion air into independently swirled secondary
and tertiary air streams, the relative amounts of secondary and tertiary air
mass flow rates being controlled by a damper incorporated into the burner
design.
Swirl control of the combustion air streams is achieved by an adjustable axial
swirl generator, a more efficient means of generating swirl compared to the
standard radial swirl generator. Swirl levels can be adjusted independently
of flow levels.
Fuel staging is achieved within the burner, by subdividing the primary
air/fuel mixture into several discrete streams, with a resultant controlled
variation of the fuel/air ratio around the primary air annulus. Coupled with
appropriate aerodynamic flow patterns produced by the swirling combustion air
and a bluff body device on the end of the primary air tube, high temperature
devolatilisation of the fuel in a reducing atmosphere occurs.
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Burner Development
Development Logic
The burner development process adopted by U.K. burner manufacturers has tended
to follow the approach of mathematical and physical modelling of a single
burner, followed by full scale single burner testing.
The Babcock Energy Large Scale Test Facility, Figure 2, is designed to allow
testing of pulverised coal burners up to 65 MW thermal input, and gas and oil
burners with a higher throughput. Low NOx burner development and
demonstration has therefore been performed at full scale, in order to
eliminate doubts on scaling parameters and to obtain representative thermal
environments.
Standard Burner Characterisation
Prior to development/demonstration of the low NOx burner in the Large Scale
Test Facility, the facility was calibrated, in terms of NOx and unburned
carbon levels, using a standard 37 MW (140,000 mBtu/hr) circular turbulent
burner. This burner was chosen for calibration purposes because over 700
burners of this thermal input are installed in U.K. power stations, both front
and opposed wall fired. A typical coal guality and fineness, (Table 1),
similar to that in the majority of U.K. wall fired power stations, was used in
the test programme.
The NOx emission levels from the standard circular burner in the test facility
compare well with data obtained from the same burner design firing a similar
coal on the Drax 660 MWe opposed wall fired boiler (1), Figure 3. Carbon in
ash and CO levels in the test facility are also broadly similar to those
obtained on the plant.
Low NQx Burner Characterisation
Figure 3 also shows the NOx/0 relationship for a 37 MW Low NOx Axial Swirl
Burner, referred to as the Mark III design, in the test facility. Fuel
quality and fineness was the same as that used for the standard burner trials.
A NOx reduction of greater than 50% was achieved on the test facility. Carbon
in ash levels were slightly higher than that associated with the conventional
burner design. In flame gaseous species measurements taken in the near burner
design, show a very high reducing atmosphere on the burner centreline, with a
very sharply defines flame envelope corresponding to the visual flame
boundary. Outside of the flame boundary the atmosphere is strongly oxidising
i.e. the reducing regions of the flame are enveloped in air.
An additional series of tests has been performed on a 48 MW Low NOx Axial Swirl
Burner in the Large Scale Test Facility to demonstrate the effect of coal
guality on burner performance. Three coals were selected, Table 2, whose
properties represent virtually the extreme, from a NOx emission point of view,
of bituminous coals fired on utility boilers and traded on the world market.
Figure 4 shows the variation of NOx emission levels with operating oxygen for
the three coals. The lowest NOx emission levels are obtained with the high
volatile coal, the NOx emission level increasing as the volatile matter
content decreases.
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Operational Experience with Low NOx Burner retrofits
Retrofit Plant
The first commercial retrofit of the Mark III Low NOx Axial Swirl Burner was
to one of the 660 MWe units at National Power's Drax plant in the U.K. Since
that retrofit in 1989, orders and options have been received for burner
retrofit to over 17,000 MWe of plant. These plant can be subdivided into
distinct groupings, as follows:-
1. The six 660 MWe opposed wall fired units, of BEL design, operated by
National Power at Drax in the U.K. These are very highly rated (burner
zone heat release ratio 1.45 MW/m ) natural circulation opposed wall
fired boilers, firing a typical U.K. bituminous coal.
2. The twelve 500 MWe front wall fired units, of BEL design, operated by
PowerGen and National Power at Ratcliffe, Ferrybridge and Didcot in the
U.K. These units are all of natural circulation design, firing typical
British coals.
3. The four 680 MWe and the four 350 MWe opposed wall fired power stations
at Castle Peak, operated by China Light and Power in Hong Kong. The 680
MWe units are very highly rated having a burner zone heat release rate of
2.0 MW/m , and are designed, by BEL, to fire over forty world traded
bituminous coals. For guarantee purposes in the low NOx burner retrofit,
Indonesian, Australian and South African coals were selected by China
Light and Power.
4. The two 375 MWe opposed wall fired once through boilers at
Studstrupvaerket, operated by Midtkraft, and designed by Deutsche
Babcock. These boilers are also highly rated, and are designed to fire a
range of international traded coals. For guarantee purposes, US and
Colombian coals were selected by Midtkraft in the the low Nox burner
retrofit.
5. Smaller single wall fired units in France and Poland. These smaller
units are of interest in that some of then have had overfire air
installed in parallel with low NOx burners.
Retrofit experience from each of the four major sub-groupings above is
summarised in the following sections.
Drax Power Station
Plant Description. There are six 660 MWe boiler units of BEL design at Drax
Power Station. Operational experience with all six units now covers over
500,000 hours service. They are of the natural circulation type and operate
at a superheater outlet pressure of 165.5 bar, and 568°C steam temperature.
The furnace design is highly rated, being designed for maximum combustion
efficiency, having a burner belt heat release rare of 1.45 MW/m . The furnace
chamber of each boiler is divided by a partial central division wall, which
cannot be sootblown. Thirty standard Babcock Energy circular turbulent
burners, supplied by five mill groups are arranged in five horizontal rows on
the furnace front wall, and thirty on the furnace rear wall. Each burner row
is fed from one mill, there being ten Babcock Energy IDE vertical spindle
mills in total. The full specified range of coals can be covered at MCR with
nine mills; for the typical design coal MCR can be achieved with seven or
eight mills in service.
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Air supply to each mill group of burners is controlled by individual dampers
to each windbox/mill group. Each burner has a central oil light up burner
with an integral core air fan to provide stoichiometric combustion air for the
oil burners.
Preconversion Performance. At 100% boiler load and 3% O at the economiser
outlet, preconversion NOx emission levels were 832 ppm (I.151b/mBtu) with the
eight top mills firing, and 747 ppm (1.041b/mBtu) with the eight bottom mills
firing. Combustion efficiency loss was typically 0.3 to 0.4% GCV, which
corresponds to approximately 1% carbon in ash. Fuel characteristics, which
are typical of the fuel normally fired at Drax, are presented in Table 1.
Burner Retrofit Results. Operational experience with the Low NOx Axial Swirl
Burner retrofit to Drax Unit 6 was presented at the 1991 EPA/EPRI Symposium
(1), and is only summarised here.
Figure 5 demonstrates how NOx and unburned carbon can be optimised for the
Drax situation by adjustment of the burner settings, the results obtained on
the plant reproducing the characteristics of the burner in the test facility.
'.V : '
The results of the demonstration tests performed with the optimised Mark III
burner are presented in Figure 6. Overall NOx levels with the eight top mills
firing are reduced from 832 to 388 ppm (0.53 Ib/mBtu), a reduction greater
than 50%, the figure obtained with eight top mills in service being just about
equal to the current EC directive for new boiler plant. CO levels are
typically 5-10 ppm at normal operating oxygen levels. Carbon in ash levels
have increased from I to 1.5% preconversion to around 2.5% with the Mark III
burner design. However, greater furnace heat absorption and consequent
reduction in gas temperature leaving the airheaters have offset this
efficiency loss.
The other subsequently retrofitted boiler units at Drax display the same
retrofit performance as Unit 6.
Ratcliffe Power Station
Plant Description. There are four 500 MWe boiler units of BEL design at
Ratcliffe on Soar Power Station, ordered in 1964. The boilers are of the
natural circulation type and operate at a superheater outlet pressure of 165
bar, and 568°C steam temperature.
Forty eight standard Babcock Energy circular turbulent burners, supplied from
eight mill groups, are arranged in four horizontal rows on the furnace front
wall. Each burner row is fed from two mills, there being eight Babcock Energy
10E vertical spindle mills in total. The full specified range of coals can be
covered at MCR with seven mills; for the typical design coal MCR can be
achieved with six mills in service.
Air supply to each mill group of burners is controlled by individual dampers
to each windbox/mill group. Each burner has a central oil light up burner
and integral core air fan.
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Preconversion Performance. At 100% boiler load with six mills in service, and
3% 0 at the economiser outlet, NOx emission levels were 560 ppm (0.77
Ib/mBtu). Carbon in fly ash levels were typically 3.5%, the fuel being fired
having a similar analysis to that presented in Table 1 but with a slightly
coarser fuel particle size distribution.
Burner Retrofit Results. Forty eight Mark III Low NOx Axial Swirl Burners
were retrofitted to Ratcliffe Unit 2 in June 1991. As in Drax Unit 6 no
significant modifications were made to the pf pipework or windbox
configuration to accommodate the Mark III design. All forty eight burner
quarls were modified to the leading front edge tube concept (1), to ensure
that the desired guarl geometry was obtained and also to eliminate the
possibility of any deposit build up interfering with the near burner air flow
pattern.
A similar optimisation exercise to that described previously for Drax Unit 6
(2) was used in the Ratcliffe burner retrofit, demonstrating the effect of
burner settings on overall NOx emission levels and unburned carbon. Overall
NOx levels were, Figure 7, reduced to 360 ppm (0.5 Ib/mBtu) at 3% operating O
(1), with boiler exit CO levels being 40% of the preconvefsion levels. Carbon
in fly ash levels have increased to approximately 6 to 7%. Overall boiler
efficiency, excluding the carbon loss, has remained substantially unaltered.
As in the case of Drax Unit 6, there has been a slight change in the
distribution of heat pick up within the boiler, the furnace being more
effective than before. These changes have not posed any operational problems
on the plant. Ratcliffe Unit 3 is scheduled for conversion later this year.
Castle Peak B Power Station
Plant Description. There are four 680 MWe units, of Babcock Energy design, at
China Light and Power's Castle Peak 'B' Station in Hong Kong, which were
brought into operation over the period of 1985 to 1989. The boilers are of
the natural circulation type and operate with a superheater outlet pressure of
170 bar, and 541°C steam temperature. The furnace design is very highly
rated, having a burner zone heat release rate of 2.0 MW/m . Twenty four
standard Babcock Energy circular turbulent burners, supplied by four mill
groups, are arranged in four horizontal rows on the front wall with a further
eighteen burners arranged in three horizontal rows on the rear wall. Each
burner row is fed from a Babcock 10.9E11 vertical spindle mill. Typically MCR
can be achieved with six of the seven mills in operation.
The air supply to each mill group of burners is controlled by individual
dampers to each windbox/mill group. Each burners has a central oil burner, of
Babcock Energy steam atomised Yjet design, capable of providing up to 42 MW
(87% of burner heat input) on heavy fuel oil. A wide range of coals, covering
forty nominated fuels from a number of different countries, is burned at
Castle Peak 'B1.
Preconversion Performance. Preconversion tests at 100% boiler load, with six
mills in service, were performed over the anticipated extremes of the fuel
range, from a NOx point of view. At 3% O at the economiser outlet, NOx
levels with the lower volatile South African coal were 850 ppm (6% 0^ dry)
(1.4 Ib/mBtu), with 750 ppm (1.25 Ib/mBtu) being achieved with the high
volatile Indonesian fuel. Carbon in fly ash loss at the same oxygen level was
typically 2.7% and 2.6% respectively.
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Burner Retrofit Results. In February 1992, Boiler B4 was retrofitted with low
NOx burners. No modifications were made to the pf pipework or windboxes, and
a philosophy was adopted of reusing as much of the original equipment as
possible e.g. core air fans, oil burner retraction equipment etc. In order to
accommodate the slightly larger throat diameter of the low NOx burners, the
refractory throat tiles were modified, and the leading front edge tube concept
introduced.
A similar but more extensive series of burner optimisation trials to that
performed on Drax Unit 6 and Ratcliffe Unit 2 were undertake on the Boiler B4
burners. Of particular interest in this situation was whether or not one
burner setting could be used for the wide range of fuels fired at Castle Peak,
in terms of optimum NOx and unburned carbon performance. To this end an
extensive series of optimisation tests were performed on Boiler B4 with three
different coals, i.e. low volatile, medium volatile and high volatile. The
results demonstrated (2), that the same burner setting could be used for each
of the coals, without a significant deterioration in burner performance from
the optimum value for any of the coals in the coal range tested.
Subsequent to the completion of the optimisation testing,-'demonstration tests
were performed with each of the fuel types. The results of the demonstration
tests, summarised in Figure 8, show the following NOx levels at around 3%
operating oxygen at the economiser outlet:-
Indonesian Coal NOx 244 ppm 6% 0 , (0.4 Lb/mBtu)
Australian Coal NOx 320 ppm 6% Q , (0.53 Ib/mBtu;
South African Coal NOx 477 ppm 6% O , (0.8 Ib.mBtu)
Overall NOx reductions of some 40 to 70%, depending on coal type, have been
achieved, with carbon in fly ash levels below the guarantee level of 5% and
not significantly higher than the preconversion levels.
Whilst no problems were experienced with the actual flame stability over the
operating load range, some problems have been encountered with ensuring
reliable flame monitoring over the range of coal types fired, particularly at
lower boiler loads. Alteration of flame monitor viewing position closer to
the root of the flame, via the secondary air register, has resulted in an
improvement in the situation, although the flame monitor signals associated
with the low NOx burner tend to fluctuate more than those associated with the
standard burner, especially at lower boiler loads.
All B station boilers have now been retrofit with low NOx burners. Similar
boiler operation characteristics have been found at Castle Peak B4 and the
other retrofitted 'B' station boilers as those noted in previous retrofits in
the U.k. at Drax and Ratcliffe Power Stations, in that the furnace chamber has
become more effective from a heat transfer point of view. It has also been
possible to simplify the boiler hot start up sequence following the
installation of the low NOx burners.
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Castle Peak A3
Plant Description. There are four 350 MEe units of BEL design at China Light
and Power's Castle Peak 'A' Station in Hong Kong. The boilers are of the
natural circulation type and operate with a superheater outlet pressure of 170
bar, and 540°C steam temperature. The furnace design is highly rated, having
a burner zone heat release rate of 1.7 MW/m . Eighteen standard Babcock
Energy circular turbulent burners, supplied by three mill groups, are arranged
in three horizontal rows in the front wall, with a further twelve burners
arranged in two horizontal rows on the rear wall. Each burner row is fed from
a Babcock 10E10 vertical spindle mill. Typically MCR can be achieved with
four of the five mills in operation.
The air supply to each mill group of burners is controlled by individual
dampers to each windbox/mill group. Each burner has a central oil burner. A
similar wide range of coals is burned on the 'A' station as on the 'B'
station.
Preconversion Performance. Preconversion tests at 100% boiler load with four
mills in service, were performed over the anticipated extremes of the fuel
range, from a NOx point of view. At around 3% 0 at the economiser outlet,
NOx levels with the lower volatile South African coal were 682 ppm (6% 0 dry)
(1.14 Ib/mBtu), with 643 ppm (1.07 Ib/mBtu) being achieved with the high
volatile Indonesian fuel. Carbon in fly ash loss at the same oxygen level was
typically 2.2% and 1.5% respectively.
Burner Retrofit Results. In February 1994, Boiler A3 was fully retrofitted
with low NOx burners. No modifications were made to the pf pipework or
windboxes, but in order to accommodate the slightly larger throat diameter of
the low NOx burners, the refractory throat tiles were modified, and the
leading front edge tube concept introduced.
A similar extensive series of burner optimisation trials to that performed on
the Castle Peak Boiler B4 burners was perfromed on the Boiler A3 burners. Of
particular interest in this situation was whether or not one burner setting
could be used for the wide range of fuels fired at Castle Peak, in terms of
optimum NOx and unburned carbon performance, as had been demonstrated on the B
station. The optimisation test results did show that the same burner setting
could be used for each of the coals on the A station boilers without a
significant deterioration in burner performance from the optimum value for any
of the coals in the coal range tested.
Subsequent to the completion of the optimisation testing, demonstration tests
were performed with each of the fuel types. The results of the optimisation
tests, summarised in Figure 9, show the following NOx at around 3% operating
oxygen at the economiser outlet:-
Indonesian Coal NOx 240 ppm 6% 0^, (0.40 Ib/mBtu)
Australian Coal NOx 300 ppm 6% 0" (0.50 Ib/mBtu)
South African Coal NOx 410 ppm 6% o , (0.68 Ib/mBtu)
Once again, overall NOx reductions of some 40 to 70%, depending on coal type,
have been achieved, with carbon in fly ash levels below the guarantee level
and not significantly higher than the preconversion levels.
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Unit A4 at the Castle Peak B has subsequently been retrofitted with low NOx
burners, and the remaining two units are planned to be retrofit next year.
Studstrupvaerket Boilers 3/4
Plant Description. The Studstrupvaerket power plant is situated on the east
coast of Jutland in Denmark, and is owned and operated by the Midtkraft
electricity company. In addition to supplying electricity, the station
supplies heat to the city of Aarhus.
Units 3 and 4 were commissioned in 1984 and 1985, and are 375 MW coal/oil
fired, Deutsche Babcock designed once through boilers, generating steam at
540°C and 250 bar. Full load can be taken on either oil or coal.
Two rows of six burners per row are arranged in an opposed wall fired pattern,
each burner having an individually controlled and metered combustion air
supply. Burner heat rating is similar to the Drax boilers, being 1.46 MW/m .
Each row of burners is fed from a Deutsche Babcock MPS 190 mill with boiler
MCR being achieved with all four mills in service, i.e. there is no standby
mill. Each coal burner has a centrally located oil burner/ for light up and
load carrying purposes.
Prior to the burner retrofit the mills were retrofitted with a dynamic
classifier, with individual pipes from the mill outlet to each burner. It was
possible to fit the low NOx burners into the existing burner throat opening,
with only minor modifications to the throat refractory profile.
Burner Retrofit Results. In the summer of 1993, both Unit 3 and 4 were
retrofitted with Mark III Low NOx Axial Swirl burners, and burner optimisation
undertaken on the guarantee coals i.e. Colombian and US coals. The analysis
of the US coal in reproduced in Table 3. Burner optimisation on Colombian
coal proceeded normally; however it became apparent during burner optimisation
with the US coal, via thermocouples which had been attached to the front end
of the burner, that the burner front end components were overheating. Water
cooled video camera inspection of the furnace by Midtkraft staff showed that
large slag deposits had built up on the front of the burner, attached to the
flameholder.
The degree of deposit was such as to cause distortion of the burner secondary
air tube, and to damage in some cases the burner core air tube. This problem
had not occurred with any other coal type fired on the Low NOx Axial Swirl
Burner, and was initially attributed to a combination of the coal ash
properties and the stabilisation effects of the flameholder. A parallel
investigation into both these effects was undertaken, with the burner being
tested in the Large Scale Test Facility with reduced degrees of flame
stabilisation. At the same time an analysis of the coal ash properties, and
comparison with other coals was underway.
The only significant difference that BEL could identify was the Swelling
number of the coal. In the case of the US coal, the value of the Swelling
Index was greater than 6, compared to 1 for the other coals. Accordingly it
was decided to ascertain the temperature at which swelling occured, and to see
if this temperature could be related to the problem with deposition on the
burners.
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A small amount of pulverised fuel was placed in a crucible and heated over the
range 200 to 500°C. The weight loss and the size and nature of the residue
was recorded. The swelling behaviour of the US coal was dramatic, the onset of
swelling occurring at between 425 and 450°C (approximately 800°F), coinciding
with the onset of volatile release. At 500°C the volume of the sample had
increase seven fold compared to the original volume giving a fired glazed
deposit.
In comparison, the standard coal exhibited no swelling at all at 500°C,
despite a considerable weight loss.
It-was concluded that the deposit formation on the burner associated with the
US coal was associated with the swelling properties of the coal rather than
the ash properties, although the ash properties may be having a secondary
effect. It was further postulated that the problem could possibly be
eliminated by reducing the primary air temperature, and a long term trial was
simulated on one mill group with the primary air temperature reduced from 90°C
(190°F) to" 65°C (150°F). This operational technique proved to be successful
in eliminating the burner deposits, and subsequently the mill operational
logic was modified to ensure low primary air temperatures' when US coal, with a
high Swelling Index, was being fired.
Guarantee tests on both guarantee coals were successfully completed in
February 1994, slightly later than anticipated due to the problems referred to
above. At 3% operating 0 , NOx levels were as follows, well within the
guarantee values:-
Colombian Coal 382 ppm (3% 0,,) (0.53 Ib/mBtu)
US Coal 353 ppm (3% Op (0.49 Ib/mBtu)
Carbon in fly ash values were under 4% in both cases.
A second problem also arose during the course of this burner retrofit. In
this case, the boiler is capable of taking full load on oil, each burner being
the same thermal rating on oil as coal. This was the first time that equality
of heat input had occurred in the retrofit projects, and it was not possible
to run the oil burner at full load due to burner overheating problems. These
were satisfactorily resolved by introducing 'primary cooling air1 into the
primary air annulus when oil firing, in order to reduce the stabilisation
effect of the flameholder on the oil flame.
Summary of Operating Experience
As a result of the retrofit experience of Babcock Energy of Low NOx Axial
Swirl burners to the range of utility boilers and fuels described above,
certain common features are evident. In the majority of cases, the retrofits
were performed with no change to the pulverised fuel or air supply systems,
with pulverised fuel distribution to individual burners being better that ±
10% of the mean. Minimum modifications have been made to the burner throat
openings; introduction of the leading front edge tube concept has had a
significant effect on the deposition of material around the burner throat
opening. Whilst this in itself will have an impact on furnace performance,
the general improvement in furnace performance noted is attributed to the
improved control of fuel and air mixing in the low NOx burner, and to the
reduction of flame temperatures in the tail of the flame.
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It is now relatively well established that an increase in the level of carbon
in fly ash is to be expected after retrofit of low NOx burners, unless mill
improvements are made. The increase in carbon levels will again be site
specific and dependent on parameters such as fuel fineness and distribution,
furnace rating, coal properties etc. Use of other low NOx techniques (for
example two stage combustion) with low NOx burners will result in a further
increase in carbon in ash levels. It may be necessary, in these instances, to
consider improving pulverised fuel fineness and distribution in order to
restore the carbon in fly ash levels to the generally preferred level of less
than 5%.
From a boiler operator point of view, it is the BEL view that the installation
of low NOx burners has been fairly transparent.
Conclusions
Since its development in 1989, the Mark III Low Nox Axial Swirl Burner has
been retrofitted by Babcock Energy Limited to over 10,000 MW of electrical
power plants in eight countries around the world. Orders^'including options,
are in place for almost 1,400 burners covering a wide range of power plant
configurations and coal types.
In general, low NOx burners are now considered to be a mature technology,
although problems do occur, and will still continue to occur, in situations
outside the range of operating experience. In general, in the retrofit
situation, there is a trade off between the achievable NOx and carbon in fly
ash levels, and care needs to be taken to ensure that fuel and air flow
control is adequate and reproducible. NOx reductions in a burner retrofit
will range from 35 to 70%, the final NOx level achievable being not only a
function of the coal type but also the boiler configuration.
For purpose designed boilers, NOx levels of 100 to 200 ppm (6% O ) (0.15 to
0.30 Ib/mBtu) can be achieved with a combination of low NOx burners and two
stage combustion techniques.
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TABLE 1 : TYPICAL UK COAL PROPERTIES
Coal Analysis Ash Analysis
Moisture
Volatile Matter
Fixed Carbon
Ash
Nitrogen
FC/VM
Nitrogen (daf)
GCV (MJ/kg)
-5
q.
11.0 Silica
28.8 Alumina
44.2 Iron Oxide
16.0 Calcium Oxide
1.18 Magnesium Oxide
1.59 Titanium Oxide
1.64 Potassium Oxide
24.96 Phosphorus
Sulphur
57.8
24.1
8.9
1.4
1.8
0.92
3.09
0.25
0.56
Pf Fineness
% < 75 micron
% < 150 micron
% < 300 micron
66.2 - 69.3
92.5 - 93.8
99.6 - 99.8
TABLE 2 : RANGE OF COALS TESTED IN THE LARGE SCALE TEST FACILITY
Indonesian
United Kingdom South African
GCV MJ/kg
H2° %
VM
FC
Ash
"o
q.
26.55
10.5
40.5
44.7
4.2
27.13
3.4
31.5
46.8
13.2
27,12
3.1
25.3
56.4
15.2
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TABLE 3 : US CUMBERLAND COAL
Coal Analysis Ash Analysis
Moisture % 7.5 Silica % 46.98
Volatile Matter % 33.6 Alumina % 23.54
Fixed Carbon % 48.4 Iron Oxide % 18.16
Ash % 10.5 Calcium Oxide % 3.28
Nitrogen % 1.37 Magnesium Oxide % 0.99
FC/VM 1.44 Titanium Oxide % 1.03
Nitrogen (daf) % 1.67 Potassium Oxide % 1.4
GCV (MJ/kg) 28.92 Phosphorus ' % 0.48
Sulphur % 3.21
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Acknowledgements
This paper is published with the permission of Babcock Energy
Limited.
References
1. King J L, MacPhail J, "Full Scale Retrofit of a Low NOx
Axial Swirl Burner to a 660 MW Utility Boiler, and the
Effect of Low Quality on Low NOx Burner Performance". -
EPRI/EPA 1991 Joint Symposium on Stationary Combustion NOx
Control. Washington B.C. March 25 to 28, 1991.
2. King J L, "Operational Experience with Low NOx Pulverised
Fuel Burners" - EPRI/EPA 1993 Joint Symposium on Stationary
Combustion NOx Control, Miami Beach, Florida May 24 to 27,
1993.
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FIGURE 1. LOW NOx AXIAL SWIRL BURNER
AIR auoep
.xp ia-«EIGHr ?EEi
FIGURE 2. LARGE SCSLE TEST FACILITY
IOOO
_ 900
£ 800
O
Q 7M
•< soo
~
i- aoo
r ^00
a.
F - STANCARO
. LS7P - MABK
IOO
23*3
t 0, 3RY
FIGORE 3.
COMPARISON OF TEST FACILITY AND
PLANT NOx LEVELS
-------
500
a:
a
TOO
I _
Q.
Q.
00
100
SOUTH
AFP ICAN
COAL
U.K. COAL
AN
COAL
1 2 3 4 5
CUTLET OXTGSN (X CRY]
FIGURE 4. EFFECT OF COAL QUALITY ON NOx EMISSIONS
U.OSS
CLCSc
CLOSE
500 f
3 A 3.A^
OA>«=B > y 0*>««3
o I§=I 2
•* ~E3T 3
Q FEs t -i
o
«
Q 400 !
a.
a.
300
2 3 4. 5
CABBCN IN FLr ASH S
FIGURE 5. EFFECT OF BURNER OPTIKISATION -
DRAX UNIT 6
a.
a.
a
IQQOl-
300
600
-100
200
12343
iCCNCMCSS? CurLET OXYGEN (Z CRY)
FIGURE 6. DRAX UNIT 6 RESULTS
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650
,00
500
400
320
300 —
2.3 3.a 33 a 0 43
ECCNCMISES OITL£T C, CS VO. CRY)
FIGURE 7. RATCLIFFE UNIT 2 RESULTS
toaa 1
a
s
a
500
V.
QJPQST-CCNVE^SICN
SOUTH
AUS7RAJ.IAM
sao
32 c,
FIGURE 8. CASTLE PEAK B4 RESULTS
1000 -i
0
X
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