EPRI
Electric Power
Research Institute

&EPA
May 1995
                     EPRI/EPA1995 Joint Symposium
                     on Stationary Combustion
                     NOX Control
                     Book 4: Friday, May 19,1995
                     Sessions 8A and 8B
                     Sponsored by
                     Electric Power Research Institute
                     Generation Group
                     Air Quality Control Program

                     U.S. Environmental Protection Agency
                     Air and Energy Engineering Research Laboratory
                     Combustion Research Branch
                     May 16-19, 1995
                     Hyatt Regency Crown Center
                     Kansas City, Missouri

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EPRI/EPA1995 Joint Symposium on Stationary
Combustion NOX Control
Book 4: Friday, May 19,1995
Sessions 8A and 8B
May 16-19, 1995
Hyatt Regency Crown Center
Kansas City, Missouri
Prepared by
ELECTRIC POWER RESEARCH INSTITUTE

Co-Chairs
A. Facchiano, EPRI
A. Miller, EPA
Sponsored by
Electric Power Research Institute
Generation Group

U.S. Environmental Protection Agency
Air and Energy Engineering Research Laboratory

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          Session 8A
Selective Non-Catalytic Reduction

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  A SUMMARY OF SNCR APPLICATIONS TO TWO COAL-FIRED WET
                               BOTTOM BOILERS
                                   Richard Himes
                                  Dennis Hubbard
                                     Zac West
                                       Carnot
                          15991 Red Hill Avenue, Suite 110
                              Tustin, California 92680

                                    Jeff Stallings
                                        EPRI
                                3412 Hillview Avenue
                                 Palo Alto, CA  94303
Abstract

In response to NOX reductions mandated under Title I of the 1990 Clean Air Act Amendments
(CAAA), Public Service Electric & Gas and Atlantic Electric of New Jersey evaluated Selective
Non-Catalytic Reduction (SNCR) for NOX control under separate programs at Mercer Station and
B. L. England Station, respectively.  Mercer Station is comprised of twin 321 MW Foster
Wheeler coal-fired wet bottom boilers, with natural gas capability up to 100% load. B.L. England
Station has three units, two of which are cyclone boilers of 136 MW and 163 MW.  These furnace
designs are of particular interest in that nominally 23,000 MW of cyclone boiler capacity and
6,900 MW of wall- or turbo-fired wet bottom boiler capacity will be faced with NOX reductions to
be mandated under Title IV - Phase n for Group n boilers.

Both stations evaluated Nalco Fuel Tech's SNCR system using a portable test skid, with urea as
the reducing chemical. The Mercer Unit 2 demonstration was performed with a low sulfur coal
(nominally 0.8%),  while the B.L. England Unit  1 demonstration utilized a medium sulfur coal
(nominally 2.4%), and also re-injects fly ash back into the cyclones for ultimate collection and
removal as slag. To address concerns over potential Ljungstrom air heater fouling,  due to
reactions between ammonia and SOs in the air heater, and fly ash salability at Mercer Station,
both sites targeted no greater than 5-10 ppmv ammonia emissions at the economizer exit. At
Mercer Unit 2, air heater fouling was only experienced during  system start-up when the ammonia
emissions at the economizer exit were estimated at levels approaching 60 ppmv. B.L. England
Unit 1, however, experienced frequent fouling of the air heater. NOX reductions achieved at both
sites ranged between 30% - 40% from nominal baseline NOX levels of 1.1 - 1.6 Ib/MMBtu.  Each
site is currently undergoing installation of commercial SNCR systems.

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Introduction

The 1990 Clean Air Act Amendments (CAAA) will have significant impacts on the electric utility
industry. Title I of the CAAA adds new mandates for bringing all areas of the country into
compliance with the National Ambient Air Quality Standard. Under Title I, utilities with units
located in areas designated as non-attainment for ozone will be required to reduce NOX emissions
from many of their existing units. SNCR is one option for controlling NOX emissions, with the
current paper focusing on its demonstration on two wet bottom boilers in New Jersey.  These
results may be of particular interest to utilities with Phase n - Group n designated boilers (wet
bottom boilers, cyclones, and cell burners) faced with pending NOX rules under Title IV of the
CAAA. Currently there are nominally 23,000 MW of cyclone utility boiler capacity, and 6,900
MW of wall- and turbo-fired wet bottom boiler capacity that will be faced with new NOX rules
under Title IV of the 1990 CAAA.

Public Service Electric & Gas (PSE&G) performed a SNCR demonstration program at its Mercer
Generating Station hi the Summer of 1993 to evaluate its feasibility to reduce NOX. The principle
project objectives were to:

       •  determine if the SNCR technology is applicable while firing coal, gas, and a
          combination of the two fuels,
       •  document the NOX removal effectiveness,
       •  evaluate the NOX reduction possible with a maximum  ammonia slip limit of 5 ppmv at
          the economizer exit,
       •  assess any impacts of residual ammonia on fly ash resale, and
       •  establish the cost of a commercial, full-scale operation.

A test program was  performed by Carnot to establish baseline emission levels and SNCR
performance at five different load conditions,  utilizing low sulfur  bituminous coal, natural gas, or
a mixture of the two fuels. The selected boiler loads were 80, 135, 200, 220, and 321 MW, with
initial testing conducted under steady state conditions.  During the final two weeks of the test
program, the SNCR test skid was set up to follow load with minimal input from operators.  This
trial was run to observe the load-following behavior of the injection system, and to collect data on
chemical consumption during 24-hour operations.

Although SNCR has been demonstrated to work on lower temperature boilers, Atlantic Electric
had concerns that at the higher operating temperatures of cyclone boilers, the addition of NOX
reductants would not be effective at reducing NOx, and could actually increase NOX through
oxidation of the nitrogen in the reagent.  Recent kinetic modeling done by Nalco Fuel Tech, and
demonstrated on full-scale units, indicates NOX reductions are achievable above 2000°F with
higher baseline NOX levels. A one month test was done hi the spring of 1993 on B.L. England
Unit 1. Reductions in NOX of about 30% from a baseline of 1.1 Ib/MMBtu were achieved at full
load under steady state operating conditions and with optimized injector configurations. At low
load (87 MWe), NOX reductions over 40% at optimized injector configurations were achieved
from a baseline of 1.0 Ib/MMBtu. No increase in air heater pressure drop was observed during

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these short term tests, and NH3 emissions at the stack were less than 1 ppmv while post
economizer slips were maintained at less than 5 ppmv.  Higher reductions on NOX can be achieved
but at the expense of increased NH3 slip and potential boiler reliability impacts. Subsequently, a
longer term test was carried out to determine  the minimum outlet NOX emission rate that could be
achieved under full dispatch conditions. The results of the latter test, which took place from
December 1993 through March 1994, are discussed in this paper.
Unit Descriptions

Mercer Generating Station has two Foster Wheeler continuous slagging, twin-furnace steam
generating units. Units 1 and 2 are identical and rated at 321 MW net each.  Each unit's steam
generator has a capacity of 2,060,000 Ib/hr of steam at a superheat outlet pressure of 2456 psig
and an outlet temperature of 1050 F.  The reheat capacity is 1,760,000 Ib/hr of steam with an
outlet temperature of 1050 F and pressure of 445 psig.  Twelve front wall-mounted burners are
arranged on each furnace in three levels with four burners per level.  In addition, there are three
water tube division walls located above the top burner elevation and centered between each
burner row.  Mercer Unit 2 has been converted to balanced draft and modifications to the radiant
superheater have been performed to enable the unit to achieve a minimum load of 25% without
adverse effects on boiler operations. A side view detail of the reheat furnace is shown in Figure 1.
Coal is burned as the primary fuel with natural gas used as both a start-up and secondary fuel. A
typical coal analysis is presented hi Table 1.  The important distinction between Mercer and B.L.
England coals with respect to the SNCR demonstrations is the coal sulfur content. Mercer fires a
low sulfur coal of nominally 0.8%, while B.L. England fires a medium sulfur coal of nominally 2.6%.

Unit 1 at B.L. England Generating Station was designed by Babcock and Wilcox and is cyclone-
fired and rated at 138 MW gross.  The steam generator has a capacity of 980,000 Ibs/hr of steam
at 1,005°F superheat and 1,005°F  reheat temperature. Crushed coal with a maximum permitted
sulfur content of 2.8% on a monthly basis and 2.6% on a yearly basis is fired through three
cyclones.  Fly ash is re-injected through either of the two bottom cyclones. A sectional view of
the steam generator is shown in Figure 2.

The  combustion air to the unit is supplied by two forced draft fans. The fans are  designed to each
provide 60% of the combustion air required to operate the unit at full load. However, during this
period the unit was not able to achieve design furnace O2 levels of 2% at full load (138 MW
gross) due to high air heater leakage rates.  Steam air heaters are installed hi each forced draft fan
discharge duct to control the average cold end temperature of the Ljungstrom air heater elements.
The combustion air from the steam air heaters is supplied at design temperatures above 100°F to
two horizontal shaft Ljungstrom regenerative type air heaters.  The air heaters are equipped with
two water wash nozzles in the combustion air duct, one on the hot end and one on the cold end.
A water wash may be performed with the unit on line at a load of 60 MW. At this reduced load,
only one forced draft fan and 2 cyclones are required for operation.  The combustion ah" is
supplied to a common windbox which houses three lO'-O" diameter water cooled cyclone burners
arranged one above two.  Each cyclone burner is supplied by a volumetric coal feeder.

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                                     »rt« ouricr
            Figure 1
 Side View of the Reheat Furnace
 Public Service Electric and Gas
Mercer Generating Station Unit 2
               Figure 2
    Atlantic City Electric Company
E.L. England Generating Station Unit 1

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Table 1
Coal Analysis, Dry Basis
Analysis Item
% Moisture
% Carbon (Dry Basis)
% Hydrogen (Dry Basis)
% Nitrogen (Dry Basis)
% Oxygen (Dry Basis)
% Sulfur (Dry Basis)
% Ash (Dry Basis)
Btu/lb - Heating Value (Dry Basis)
Mercer 2
7.5
86.9
4.26
1.24
1.79
0.81
5.00
14,972
B.L. England 2
8.7
72.2
4.91
1.24
6.10
2.64
12.89
13,109
The combustion gases pass through a single furnace into the convective pass. In the convective
pass, the gases pass over the primary and secondary superheaters as well as a reheat superheater.
An economizer is located after the primary superheater.  The gases pass through the two
Ljungstrom ah- heaters and then the electrostatic precipitator (ESP) before exiting out the stack.

Temperature Profiles

Temperature profile data was obtained by Nalco Fuel Tech (NFT) at Mercer to provide input into
there Computational Fluid Dynamics Model (CFDM). Figure 3(a) plots the average temperature
measured at full load and low load at each port. A high velocity thermocouple, or suction
pyrometer, was used to measure furnace gas temperatures and provide a gas sample. Flue gas
temperatures at nominal full load ranged from 2000 F - 2250 F at the three ports with available
access, which were marginally downstream of the actual injector locations. At minimum load (81
MW), temperatures at these ports were reduced to 1200 F -1550 F. Similar data was taken by
RJM, a Nalco Fuel Tech licensee, at B.L. England Unit 1. As shown in Figure 3(b), a similar
range, albeit higher absolute values were encountered at four locations with available access. Full
load flue gas temperatures ranged from 1750  F  - 2500 F. Minimum load (60 MW) flue gas
temperatures were reduced to  1400 F - 2100  F.

Baseline NOx

Due to relatively small furnace dimensions  and high temperatures necessary to maintain proper
slag flow, baseline coal-fired NOX emissions at Mercer Unit 2 range from nominally 1175 ppmc
(1.6 Ib/MMBtu) at full load to 400  ppmc (0.55 Ib/MMBtu) at 25% maximum continuous rating
(MCR). A summary of the baseline NOX emissions over the entire load range is shown in Figure 4.

Atlantic Electric's coal-fired cyclone boilers at B.L. England station had average baseline NOX
emissions on the order of 800 ppmc (1.1 Ib/MMBtu). Based upon data from the plant Continuous
Emissions Monitoring System (CEMS) installed in November 1993, the variability in NOx  emissions
is quite high (Figure 5). Scatter about the mean emission level was found to be on the order of+/- 250
ppmc, representing a 40% uncertainty hi the baseline NOx value. Attempts to more quantitatively

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               ^ffi::pl::±::lf^^                          ^'dS^i
                                              Ms l,« «S-«"P ?* -¥^; 5-^ ^;V^!«
                                (a) Mercer Unit 2
                             (b) B.L. England Unit 1
                                    Figure 3
Average Furnace Exit Gas Temperatures Measured at Full Load and Low Load at Each Port

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               a^sb^y *
                                   Figure 4
                         Mercer 2 Baseline NOX Emissions
                                   Figure 5
B.L. England I Baseline NOX Emissions Based on CEMS Data from December 1-12, 1993

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define relationships between operating conditions and NOX were not successful. This inability to
correlate average NOX to load and economizer O2 is hypothesized to be a result of the cyclone
and unit specific conditions. During the long-term demonstration, baseline data were recorded
three times daily when the SNCR system was shut off for 5-30 minutes during each period.


SNCR Injection Systems

Temporary SNCR injection systems were used during both demonstrations. The system consisted
of a 21,000 gallon temporary storage tank, Nalco Fuel Tech pumping/metering control trailer,
injector distribution modules and air-atomized injectors. The pumping and metering trailer
included a tank recirculation pump, electric heater and chemical pumping and metering skids. The
trailer was also equipped with a control panel to properly meter the chemical flow rate to the unit
in the proper proportion with the dilution water. The injection trailer was equipped with a water
pump and a static mixer to mix and deliver the diluted reagent to the injectors. The injection skid
was capable of providing independent flow and concentration control to each level of injectors.
The chemical solution was transported to the boiler by two 1-1/2 inch stainless supply pipes.
Each pipe represented a zone in the control scheme of the demonstration trailer.  At each level,  a
distribution module received the water/chemical mixture and metered the flow to each lance.
Each lance had an indicator for both air and chemical flow.

At Mercer, three levels of injectors were initially specified based on available ports and modeling.
Four additional ports were added during testing.  The initial ports were located at elevation 208'
(Level 8) on the front wall, elevation 195' (Level 7) on the front wall, and 186' (Level 6) on the
rear wall.  Each wall had four lances. Level 8 was shown to help reduce NOX emissions, but only
with high ammonia slip rates.  Upward-angled lances were added at elevation 172' (Level 5) in an
attempt to obtain reduction levels similar to Level 8, but with lower slip rates.  Level 5 was
comprised of two lances on the front wall and one on each side wall.

At B.L. England, the injector distribution modules were located on the 6.5 (Level 1) and 8th
(Level 2) floor elevations, and controlled the atomizing air and chemical flow rate to the
individual injectors.  A total of 17 injectors were installed on the unit through a combination of
new and existing observation ports. The Level 1 injectors were controlled by two injector
distribution panels, one controlling six injectors along the front wall and one controlling three rear
wall injectors and two side wall injectors.  The Level 2 injectors were controlled by a single
distribution panel which fed six injectors along the front wall above the nose of the boiler. These
injection ports  were the same as those used in the short-term test and were installed based upon
temperature measurements and the Nalco Fuel Tech CFD and CKM Model recommendations.
Figure 6 is a diagram of the NOXOUT® Process installed on Unit 1.

Control of the  SNCR systems were performed by use of a steam flow signal and NOX
concentration feedback signal. The steam flow was characterized in segmented ranges to the
proper level of injection and NOX setpoint with attendant maximum and minimum reagent
pumping rates.  These pumping ranges were designed to limit ammonia slips and  were based upon
short term tests. A corrected NOX concentration from the plant CEMS was tied into the control

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   PLANT ATOMIZING AIR
     MIXED CHEMICAL
       TO LEVEL 2
         MIXED CHEMICAL
           TOLEVEL1
         NALCO FUEL TECH
           FC-103 NO.OUT
         TESTING TRAILER
         NO.OUTA  I
         RETURN
     LEVEL 2 WALL
     DISTRIBUTION
       MODULES
     LEVEL 1 WALL
     DISTRIBUTION
       MODULES
     LEVEL1WALL
     DISTRIBUTION
       MODULES
                   \
  SO% SOLUTION
|1  LQ
OLUTTON)
  uO
                   1
CHEMICAL
PUMPING
 EQUIP.
     (JO
                                                 LEVEL 2 WALL
                                                 INJECTORS (8)
                                  B.L. ENGLAND UN1T1
                                  138 MWg COAL-FIRED
                                    CYCLONE BOILER
                                          LEVEL 1 WALL
                                          INJECTORS (6)
                                                LEVEL 1
                                                 WALL
                                        INJECTORS
                                            (5)
 CONTAINMENT BASIN
                      NO.OUT A SUPPLY
               DILUTION WATER

               PLANT PROCESS & CONTROL SIGNALS
                     (BOILER LOAD ft TRIPS)
                                     Figure 6
                   NOXOUT Process Diagram at B.L. England Unit 1

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as feedback for reagent pump rate trim within the limits established by the load.  The pump rates
and the injection levels used at the different steam flows were determined as testing proceeded, in
order to attain NOX setpoint while minimizing ammonia slip.
Test Conditions and Results

At Mercer, the SNCR system was tested for NOX reduction at specific load and fuel conditions.
Figure 7 shows a grid of coal-fired test conditions and the amount of NOX reduction achieved. As
indicated the range of coal-fired NOX reductions ranged from 32% to 38% with normalized
stoichiometric injection ratios (NSRs) of 0.8 - 1.2. The principle factor establishing the maximum
NSR was the maintenance of the ammonia slip at or below 5 ppmv. Deliberate attempts to reach
increased slips of 15 ppmv were tried over short time spans at some loads and conditions. Under
100% coal-fired operating conditions, the NSR was increased from 1.2 to 1.83 at 80 MW with
NOX reductions increasing from 32% to 46%.  The chemical utilization between these two tests
was reduced from 27%  at a NSR of 1.2 to 25% at 1.8, thus the principle limiting factor to
performance is the ammonia slip value which does not impair boiler operating reliability due to air
heater fouling or ash resale.

At B.L. England, the objective for the longer-term test was to demonstrate what reduced NOX
emission rate could be maintained under economic unit dispatch.  Some of the specific concerns
that could not be addressed in the conceptual test that needed to be addressed in the longer-term
test were load following and area  regulation requirements and the impact of various levels of
resulting ammonia slip on air heater fouling.

As previously mentioned, the longer-term test took place from December 1993 through March
1994. During December, only baseline testing was done with urea injection limited to  setting
injection pressures and flows. Urea injection under automatic control was begun in early January,
and the unit was left on economic dispatch for the bulk of the test period. To accomplish the test
goal, and due to an increased frequency of air  heater fouling with the unit operating under area
regulation, several injector configurations and NOX setpoints were evaluated.  A summary of these
test conditions is presented in Table 2.

The stack NOX emission value that could be maintained was found to be dependent on several
parameters. These include:  (1) the ability of the SNCR control system to react to changing unit
conditions and hold a given setpoint; (2) combustion conditions such as fuel-to-air ratios, flue gas
temperatures, CO and SO3; (3) secondary effects such as NH3 slip, ammonia/ash recycle, ambient
conditions and air heater fouling.

The ability to control to a NOX emission rate during the long term demonstration was limited to a
few controllable process variables. SNCR process variables including injector location, style and
nozzle tip orientation, dilution water flow rate and atomization pressure were optimized and fixed
for the test condition. The real time, controllable parameter remaining was  reagent injection rate
to either or both injection levels. Reagent injection rates  were determined by the controls based
on setpoint, NOx,  steam flow (load), and O2. The test period was split into  eight operating

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periods, characterized by injection configuration, NOX setpoint and boiler conditions with regard
to excess 62, as defined in Table 2. Other factors impacting the operation of the SNCR system
during the long- term demonstration are listed, chronologically, in Table 3.  It should be noted
that limitations imposed by the design of the temporary injection system restricted the ability of
the process to respond rapidly to changes in boiler conditions.  Some of these limitations can be
minimized in a full scale commercial installation.
Fuel/Load
100%Coal<5ppm
NHa Target




100% Coal <15ppm
NH3 Target




80 MW
NOxRed-32%
NH3 Slip - 7.8 ppm
NOxtoN2O-35.0%
NSR-1.2
Utilization - 27%
2Sep93
NOxRed-46%
NH3 Slip - 17.5 ppm
NOxtoN2O-34.4%
NSR-1.83
Utilization - 25%
2Sep93
135 MW
NOxRed-37%
NHs Slip - 2.3 ppm
NOxtoN2O-10.5%
NSR-0.82
Utilization - 45%
24Aug93
Not Tested





200 MW
NOxRed-38%
NH3Slip- 1.4 ppm
NOxtoN2O-7.0%
NSR-0.78
Utilization -44%
18Aug93
NOxRed-51%
NH3 Slip - 3.3 ppm
NOxtoN2O-5.6%
NSR-1.63
Utilization -31%
10Sep93
220 MW
NOxRed-34%
NH3 Slip -4.1 ppm
NOxtoN2O-7.0%
NSR-0.78
Utilization - 44%
18Aug93
Not Tested





321 MW
NOxRed-37%
NHs Slip - 4.0 ppm
NOxtoN2O-7.7%
NSR-1.17
Utilization -31%
17Aiig93
Not Tested





                                        Figure 7
   Mercer 2 NOX Reduction Under 100% Coal-Fired Test Conditions (Steady State Operation)
                                        Table 2
                   A Summary of Test Conditions at B.L. England Unit 1
Period
Date
Injection
Configuration
NOX Setpoint
(Ib/MMBtu)
Boiler Conditions
    1         Jan. 6 - Jan. 21
    2         Jan. 25   Feb. 8
    3        Feb. 9 - Feb. 16
    4        Feb. 17 - Mar. 2
    5        Mar. 2 - Mar. 9
    6        Mar. 9-Mar. 15

    7       Mar.  15-Mar. 26
    8       Mar. 26 - Mar. 29
2 Levels
 1 Level
 1 Level
 1 Level
 1 Level
 1 Level

2 Levels
2 Levels
      0.75
      0.82
      0.75
      0.68
      0.61
 0.61 60-100 MW
0.68 100-132 MW
      0.68
      0.82
 LowOz
 Low O2
 Low O2
Design Cb
Design C>2

Design Cb
Design O2

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                                               Table 3
	Chronologicalj.is^ofFactors Impacting B.L. England Unit SNCR Demonstration
 Date          Event
 1/6 -1/25      Setpoint 0.75 Ib/MMBtu, 2 Level Injection
 1/6 - 3/2       Large 62 swings resulting in very low boiler Oj
 1/7           Fluctuating air pressure to injectors
 1/7 - 2/4       Urea flow rate unstable
 1/10          Increase in air heater pressure drop
 1/10 -1/21    Low average Oj resulting from air heater plugging and loads in excess of 130 MW
 1/13          Reduce minimum SNCR operating load to 60 MW
 1/20 -1/25    Air heater sootblowers out of service
 1/21          Upper level minimum flow rate decreased. Lower level water flow rate increased
 1/25          Air heater water wash
 1/25          Setpoint raised to 0.82 Ib/MMBtu. Lower level injectors only
 1/27          Decreased water pressure to injectors
 2/5           Air heater water wash
 2/9           Setpoint changed to 0.75 Ib/MMBtu
 2/16          Setpoint changed to 0.68 Ib/MMBtu
 2/21          Air heater water wash
 2/28 - 3/2      Total flow rate to injectors 1.45 gpm
 3/2 - 3/9       Injector flow rate decreased to less than 1 gpm
 3/2           SNCR system controlling off of west econ. 02
 3/2           Setpoint changed to 0.61 Ib/MMBtu
 3/4           Maximum load limited to 128 MW
 3/4           Operating at design 02 conditions
 3/9           Increased maximum injection rate at steam flows above 635 Klb/hr
 3/9           Increased water injection pressure
 3/9           Setpoint changed to 0.68 Ib/MMBtu at steam flows above 745 Klb/hr
 3/4 - 3/15      Maximum load reduced from 128 MW to 110 MW due to air heater plugging
 3/15          Water pressure increased to injectors; 1 gpm/injector, 30 psig air
 3/15          Setpoint changed to 0.68 Ib/MMBtu. Second level in service
 3/16          "A" air heater water washed
 3/17          "B" air heater water washed
 3/19          Economizer Oj control disconnected
 3/21          Air pressure increased from 30-45 psig on level 2
 3/26          Setpoint changed to 0.82 Ib/MMBtu

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Though conditions throughout the test were not always representative of target operating
conditions, the SNCR system was able to demonstrate overall reductions hi NOX. Such
reductions were more significant at lower load, but, on average, indicate that a 30% reduction in
NOX should be achievable under dispatch conditions (Figure 8) while simultaneously maintaining
NH3 slip at a level which minimizes air heater fouling.  From an average baseline of 1.1 Ib/MMBtu
during the test, the system could generally average NOX emissions around set points of 0.75-0.82
Ib/MMBtu. During these periods, the chemical usage corresponded to an average NSR of 0.7.
Air Heater Fouling

At Mercer, no problems were experiences during the SNCR demonstration with increased air
heater pressure differential except during one excursion of ammonia emissions during the
optimization phase of the program.  During this condition the ammonia slip was approximately 60
ppmv, and exhibited corresponding increases in the air heater differential pressure. When soot
blowers were employed and the slip rate was returned to the 5 ppmv target level, the differential
pressure returned to normal.  It should be noted, however, that the bulk of the tests were
performed under steady state operating conditions, and only involved load following during the
last two weeks of the demonstration.  Although the results are indicative of limited air heater
fouling problems with a low sulfur coal, the operating experience under transient load following
conditions is limited.

Air heater fouling at B.L. England occurred four times over the course of the long-term
demonstration. A chronology of air heater washes during SNCR operations is shown in Figure 9.
Water washes are typically performed when the furnace pressure approaches 20 in.H2O at full
load, which corresponds to pressure drops of 9 to 10 in. H2O across the air heaters. The average
number of SNCR system operating hours before water washing was required was 274 hours as
compared to 1,038 hours during unit operation without  chemical injection.  The fouling of the air
heaters resulted from ammonium sulfate and bisulfate formation and possibly increased ash
cohesiveness due to the elevated NH3 levels on the ash.  The air heater fouling was likely
compounded by low air temperatures exiting the steam coils during periods of low ambient air
temperature (<20°F)  and periods when the steam coil air heater was out of operation.

Sootblowing did not appear to reduce the air heater fouling after an increase in the pressure drop
was noticed.  Optimizing the frequency of sootblowing and steam pressure to the sootblowers
may have the potential to improve the time between air heater washes, but is not expected to
improve the ability to remove deposits in the intermediate air heater baskets and deep within the
cold-end air heater baskets. The increased ah- heater pressure drop also exacerbates the existing
problem with limited fan capacity at full load. Increases in fan horsepower and parasitic loss of
power will be a potential added cost and impact of SNCR for NOX control at B.L. England.

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      1000
   8
   £
   Q.
   in
   O
   in
   J2
   UJ
   5
                                                           Baseline NOx
                                                       -A-NOxwithSNCR
                                                       -A-NH3Slip
          80
90
100
   110
Load (% MCR)
120
130
140
                                   Figure 8
Summary of NOX Reduction and Ammonia Slip During B.L. England 1 SNCR Demonstration

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                                   WASH
                                                W WASH
 	1	'	l""l	I	.....f.............I	...I
1/6     1/15          1/312/6      2/16          3/1         3/16        3/29

                                   DATE
                                  Figure 9

                SNCR Operating Periods with Air Pre-Heater Washes

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SNCR Capital and Operating Costs

The costs involved with the procurement, operation, and maintenance of the SNCR system may
be divided into several categories. They are the capital costs incurred for the design and
installation of the system, the chemical costs required for system operation, costs associated with
the operation of the urea heater, injection pumps, and associated equipment, labor costs for
required maintenance, and costs due to boiler efficiency penalties.  To determine the cost
associated with each category, the following assumptions and operating parameters were
used.The capital costs for a commercial system at Mercer (321 MW) and B.L. England (138
MW) have been estimated at $3,400,000 ($10.6 $/kW) and $2,070,000 ($15/kW) respectively.
Included is the equipment, engineering and design, installation and start-up services, one year
service contract, as well as the licensing fee.

The boiler heat rate penalties resulting from the vaporization of the aqueous solution decrease the
boiler efficiency by approximately 0.5%. At Mercer, this is based upon 24 injectors discharging 1
gpm/injector, resulting in a total liquid flow of 24 gpm. At B. L. England it was assumed that
multi-level injection would be used for the commercial installation, with each injector discharging
1 gpm/injector on the lower elevation and 0.6 gpm/injector on the upper elevation, resulting hi a
total liquid flow of 15 gpm.

A summary of the cost estimates for the installed SNCR system at each site is presented in Table
4. The analyses are based on the above assumptions, a plant capacity factor of 60%, and an
annual capital recovery rate of 14.67% was used.

Based on this analysis, the total SNCR annualized cost would be $1.4 million per year, or $937
per ton NOX removed.  Of this total, 22% is capital investment, 59% is reagent cost, and the
remaining 19% represents maintenance, power requirements, and boiler efficiency penalties.

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                                        Table 4
                  Estimated Cost Analysis for Commercial SNCR Systems

Uncontrolled NO*, Ib/hr, (Ib/MMBtu)
Controlled NOx, Ib/hr, (Ib/MMBtu)
NOX Removed, tons/yr
Reagent Use, gal/hr
Reagent Cost(1), $/yr
Water Cost(2), $/yr
Capital Cost, $/kW
Capital Cost
Annualized Capital Investment
Maintenance, $/yr
Power Requirements^, $/yr
Boiler Efficiency Penalty, MMBtu/yr
Boiler Efficiency Penalty(4), $/yr
Capital and O&M Costs, $/yr
Total Cost, $/Ton NOX Removed
Mercer
Unit 2
5,008(1.6)
3,155 (1.0)
4,870
660
2,567,000
13,665
10.6
3,400,000
498,780
178,500
18,600
82,000
137,350
3,414,000
701
B.L. England
Unitl
1,794 (1.3)
1,242 (0.9)
1,451
206
801,225
9,248
15
2,070,000
303,669
85,000
8,000
57,000
95,500
1,360,000
937
(1) NOXOUT HP reagent cost of $0.74/gal.
(2) Based on water cost of $2/1000 gallons
(3) Based on energy cost of $0.03/kWh
(4) Fuel cost of $1.675/MMBtu
Summary And Discussion

At Mercer 2, NOX emissions were reduced by an average of 36% while maintaining the ammonia
slip at or below 5 ppmv, corrected to 7% O2. The NSR corresponding to these operating
conditions ranged from 0.8 - 1.2, with the average over the load range being 1.0.  Chemical
utilization was varied with load and injection temperature, but averaged 36%.  Additional tests
performed at higher ammonia slip levels indicated that increased NOX reductions were feasible.
Under coal-fired conditions, only two loads (80 MW and 200 MW) were investigated in this
regard with NOX reductions ranging from 46% to 51% at a NSR of 1.8 -  1.6 respectively.  The
corresponding ammonia slips were 17 ppmv and 3 ppmv. In general, the low sulfur coal fired at
Mercer Station did not present any operating limitations within the range of conditions tested with
respect to air heater fouling or fly ash resale impacts.

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The SNCR demonstration at B.L. England Station, on the other hand, exhibited an increased
sensitivity between coal sulfur level (e.g. flue gas SO3 concentration) and ammonia from the
SNCR process. The following is a summary of performance along with any associated boiler
impacts:

•  the system was able to maintain an average reduction of 30% during the test while maintaining
   NH3 slip at less than 10 ppmv.  For a representative baseline 1.3 Ib/MMBtu, one could expect
   to maintain an average emission rate of 0.9 Ib/MMBtu under dispatch conditions as one
   approach to minimize ammonia slip and air heater impacts.

•  the SNCR system was unable to control to tested NOX setpoints below 0.9 Ib/MMBtu at loads
   above 120 MW with stack O2 levels in excess of 9.6% while simultaneously maintaining NH3
   slip at less than 10 ppmv.
•   load changes induce wide variations in NOx, and NOX changed more rapidly than the
    temporary SNCR system could respond:  These together limited how closely NOX could be
    controlled. Nalco Fuel Tech and RJM both believe that improvements (reductions in response
    tune) can be included in a commercial injection and control system.

•   over control of NOX at loads below 100 MW will help compensate for the inability to control
    NOX at high levels of excess air and load over a 24-hour period.

•   air heater fouling from the deposition of ammonium bisulfate increases regardless of setpoint
    or injector configuration; an acceptable, and controllable, level of ammonia slip appears to be
    less than 10 ppmv but needs to be tested further. Ah- heater fouling during the test periods
    was probably exacerbated by low ambient air temperatures and failure of the steam coil air
    heater.

•   flyash reinjection eliminates problems associated with elevated NH3 content of the fly ash

Based on the test results, none of the injection configurations are capable of controlling NOX
below a 0.90 Ib/MMBtu setpoint without impacting the boiler reliability.  All configurations tested
increased the rate of air heater fouling and caused elevated concentrations of NH3 on the fly ash.

The system could not maintain NOX setpoints below 0.82 without sacrificing excess O2, load or
NH3 slip.  Upward adjustments of excess O2 and/or conditions of high baseline NOX generally
resulted in periods in which the setpoint could not be maintained.  Such instances of high NOX
were observed in seven of the eight periods, with each exhibiting controlled NOX levels
approaching 0.9 Ib/MMBtu.

In comparing these two demonstrations, it is important to note that although the SNCR is  a
commercially viable technology and is being installed at both of these stations on a commercial
basis, the results obtained are site specific hi nature. As has been documented in the literature, the
NOX reduction performance potential of SNCR is a function of both SNCR process  chemistry and
furnace parameters.  The following factors are relevant:

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       •  chemical type,
       •  amount of reagent,
       •  injection temperature(s),
       •  residence time, velocity,
       •  initial NOX level,
       •  additive/trace gas species,
       •  injection/mixing system, and
       •  fuel effects.

These two demonstrations employed a similar test skid from Nalco Fuel Tech, using urea at
comparable injection rates, on boilers that exhibited similar initial NOX levels and temperature
windows.  One significant difference is the coal fuel sulfur level used at the two sites.  The sulfur
content and trace metals in the fuel will affect the formation of SO3, which reacts with unreacted
ammonia to form undesirable deposits at low temperatures. The amount of 863 can constrain the
concentration of unreacted ammonia, which can in turn constrain the amount of reagent and
achievable NOX reductions. Based on these two SNCR demonstrations, the achievable NOX
reduction with a high sulfur coal boiler operating is uncertain. The data from these two suggests
that unless SOs interactions with ammonia can be addressed beneficially, NOX reductions may be
limited below typical levels obtained at low sulfur application sites.  It is thus important for
regulators to understand the site specificity of the SNCR technology performance when applied to
the vast range of coal-fired utility boiler designs and fuel properties.
Acknowledgments

The authors would like to thank Frank Gibbons, Al Wallace, and Alex Huhmann of Public Service
Electric & Gas, Debra Mellish and Mike Cunningham of Atlantic Electric, Giff Broderick of RJM,
and John O'Leary of Nalco Fuel Tech for their efforts during the actual test programs and their
contributions to the review provided for this paper, and the respective test reports.
References

Gibbons, F.X., et.al., "A Demonstration of Urea-Based SNCRNOX Control on a Utility
Pulverized-Coal, Wet-Bottom Boiler," EPRI Workshop - NOX Controls for Utility Boilers, May
11-13, 1994, Scottsdale, Arizona.

Hubbard, D. G., et.al., "SNCR Demonstration of NOX Control for a Cyclone-Fired Boiler Burning
High Sulfur Coal," AFRC/JFRC Pacific Rim International Conference, October 16-20, 1994,
Maui, Hawaii.

EPRI Report TR-105068, "Long Term SNCR Demonstration at B.L. England Station Unit 1."

EPRI Report TR-105071, "Demonstration of a Urea-Based SNCR Technology on a Pulverized,
Coal-Fired, Wet-Bottom Boiler."

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    DESIGN OPTIMIZATION OF SNCR DENO. INJECTION LANCES
                                                    X
                   Dale G. Jones, Noell, Inc., Long Beach, CA 90806
                Jochen Steinberger, Noell, Inc., Long Beach, CA 90806
             Terry Hunt, Public Service Co. of Colorado, Denver, CO  80223
         Christopher Barton, Public Service of New Hampshire, Bow, NH 03304
        Lawrence J. Muzio, Fossil Energy Research Corp., Laguna Hills, CA  92653
          Jeff Stallings, Electric Power Research Institute, Palo Alto, CA 94304
           Ron Sherrick, Diamond Power Specialty Co., Lancaster, OH 43130
Abstract

Because of the temperature sensitivity of SNCR processes, load following control to minimize
NH3 slip is a critical issue.  Advanced retractable injection lances (ARIL) provide improved
load following control for SNCR DeNOx. Using ARIL technology for SNCR DeNOx, 30% to
50% DeNOx can be achieved while limiting NH3 slip to 10 ppm.

One ARIL lance is located at each boiler sidewall, each supplied with compressed air and
liquid chemical.  A row of nozzles on the sidewall of the lance form a "jet curtain" to provide
flue gas cross-sectional coverage. Load following is provided by automatically rotating the
ARIL lances in response to a furnace exit gas temperature (FEGT)  or a boiler load signal.
Design optimization is required for most boilers, generally including field testing and cold
flow modeling. Field tests using "stub" lances have verified low NH3 slip at 40%  DeNOx or
more.  Flow model tests have shown how to optimize the location of the ARIL lances so that
improved flue gas mixing can be achieved without increasing air compressor capacity, which
is typically less than 0.2% of plant output.

ARIL SNCR DeNOx was demonstrated in 1991 at Pacific Gas & Electric Co. Morro Bay Unit
3 (330 MW).  Two additional ARIL systems have been installed on coal-fired boilers, one at
Public Service Co. of Colorado, Arapahoe Unit 4, (100 MW, balanced draft), and the other at
Public Service of New Hampshire, Merrimack Unit 1, (120 MW, cyclone-fired).  Although
the  total installed cost for smaller 100 MW coal-fired plants is about $15/kW, the  total
installed cost of ARIL technology for SNCR DeNOx  on larger plants (due to economies of
scale)  is expected to be in the range of $7/kW to $10/kW.

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Introduction

Selective Non-Catalytic NOX Reduction (SNCR) involves the selective reaction of the
decomposition production of ammonia, or urea, with NOX in the presence of oxygen.  The
process is extremely temperature sensitive, operating over a narrow temperature window of
nominally 1600 to 2200°F. The basic SNCR DeNOx reaction is

                                NO + NH  = N  + HO
                                        2    2
The amine radical (NHj) is formed by direct furnace injection of liquid ammonium hydroxide,
or urea, where the NH3 component loses a hydrogen atom, and any HNCO component reacts
to form amine radicals and other reactants.

Unreacted amine radicals form NH3 slip at the boiler economizer outlet which can react with
SO3 or HC1, etc., to form various salt compounds. Depending on where the salts form
downstream, equipment can become fouled, or plume visibility impacted due to atmospheric
condensation at cooler temperatures.  The only way to avoid undesirable ammonium salt
byproducts is to limit the NH3 slip, generally  to less than about  10 ppm at the economizer
outlet.

The NH3 slip constraint imposes a limit on the amount of NOX removal that can  be achieved
using the SNCR DeNOx process. Because the SNCR DeNOx process is temperature sensitive,
load following to maximize DeNOx while minimizing NH3 slip is a critical issue.

Advanced retractable  injection lances (ARIL) provide improved load following control for
SNCR DeNOx. There is one  ARIL lance at each boiler sidewall, each supplied with
compressed air and liquid chemical. A row of nozzles on one side of the lance form a "jet
curtain" to provide the flue gas cross-sectional coverage. Load following is provided by
automatically rotating the ARIL lances in response to a furnace exit gas temperature (FEGT)
or a boiler load signal.

Using ARIL technology for SNCR NOX reductions of 30% to 50% can be achieved with a 10
ppm NH3 slip constraint. Lower levels of NH3 slip can generally be realized using
ammonium hydroxide instead of urea, and urea is also more expensive. However, both
chemicals have been demonstrated  and can be used for SNCR DeNOx with the ARIL  lance
technology.
Design Approach

Most boilers are sufficiently different that there is no standard formula or system
configuration that can be used.  Instead, design optimization using a combination of field
testing and boiler  cold flow modeling provides assurance of improved SNCR system
performance and minimizes risk.

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Field testing includes both high velocity thermocouple (HVT) temperature measurements in
the upper furnace zone(s) of interest and preliminary SNCR field testing using short "stub"
lances.  The "stub" lances protrude approximately eight feet into the flue gas and treat a
portion of the flue gas.  This allows the local SNCR process performance (DeNOx and NH3
slip) to be measured downstream at the economizer outlet.  It has been found that lateral
mixing through the boiler convection tube banks is somewhat limited,  and a good
approximation of full-scale performance results can be obtained using this low cost field test
approach.

Boiler cold flow modeling is another important component of the design approach. The cold
flow modeling quantifies the degree of mixing that can be achieved at different boiler
sidewall locations for the ARIL lances. The degree of mixing can be improved by about 50%
if the location is optimized, compared with just locating the ARIL lances at a reasonable
position. Since secondary flows and turbulence are not accurately known a priori, the cold
flow model testing can lead to significant reductions in the electrical consumption for air
compressors.  In comparison, simply "plugging in" the ARIL lances and then performing the
required optimization testing at full scale provides a significantly increased risk of having to
relocate the ARIL lance position(s).
Field Testing Results

An SNCR system utilizing wall nozzles was installed as part of the DOE CCT HI integrated
emission control system at PSCC Arapahoe Unit 4 (100 MW coal-fired).  As a result of the
low-NOx burner retrofit, the furnace exit gas temperature dropped by almost 200°F. This
drop in temperature compromised the low load performance of the SNCR system with the
existing wall nozzles.  To improve SNCR performance at low loads, an ARIL lance system is
being installed using two existing furnace side wall ports. The SNCR injection locations for
this boiler are shown in Figure 1. To support the design of the ARIL  system, a  series of tests
were conducted using a "stub" lance on one side of the furnace.  An eight foot "stub" lance
was manually installed  into an observation door near the preferred location for the ARIL
lances.  The effect of "stub" lance rotation angle at 60 MW boiler load is shown in Figure 2,
where it is seen that the DeNOx can be varied between 12% and 43%  at a fixed  NSR =1.0
simply by rotating the ARIL lance.  A  better indication of ARIL lance performance is
provided in Figure 3, where the wall injectors are compared with the "stub" lance for DeNOx
and NH3 slip performance  at 60 MW load.  At a 10 ppm NH3 slip limit, it is seen  that when
using wall injectors, the DeNOx is limited to about  13%, but with the  "stub" lance, the NH3
slip was only about 7 ppm with DeNOx over 50%.  The ability to provide NH3 slip control by
automated rotation of the ARIL lance provides an important advantage for load following
operation.

A similar "stub" lance test was conducted to support the full-scale ARIL design  for PSNH
Merrimack Unit 1 (120 MW coal-fired cyclone). An eight foot "stub" lance was installed into
the upper sootblower port at the secondary superheater (SSH) tube bank (see Figure 4).
Table 1 shows the NOX removal and NH3 slip performance results obtained at an ammonium
hydroxide NSR value of nominally  1.5:

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                                      Table 1

                  "Stub" Lance Performance at PSNH Merrimack Unit 1
                    (Load: 120 MW, NO^: 900 ppm, NH^TNO,: 1.5)

        "Stub" Lance Angle          DeNOx                 NH3 Slip

   90 degrees (straight down)           33%      42 ppm (3.1% of NH3 injected)

   67 degrees (into upper furnace)       28%      25 ppm (1.9% of NH3 injected)

   45 degrees (more into U.F.)          18%      5 ppm (0.4% of NH3 injected)

   0 degrees (toward front wall)         15%      not detected
Figure 4 also shows the gradient in NOX removal measured at the economizer exit.  As can be
seen, some of the flue gas passed over the top of the stub lance with little NOX removal near
the outer wall at the economizer exit.  This clearly shows the need to optimize the SNCR
mixing processes in the temperature window.

During the field test program at Merrimack Unit 1, the vertical temperature gradient at full
load from the nose of the arch to the furnace roof (a distance of 22.7 ft.) was estimated to be
about 900°F.  This unexpected result, combined with lateral mixing and DeNOx gradient
effects measured at the economizer exit, result in the expectation that the full-scale ARIL
lances will produce about 50% DeNOx at NSR =1.5. The guaranteed NOX removal at full
load for Merrimack Unit 1 is 31% at NSR = 0.80.

The flue gas temperature for the "stub" lance tests at both sites was approximately 2100°F to
2300°F. The SNCR process seems to provide improved control  of NH3 slip and reasonable
NSR requirements for a given amount of NH3 removal when the injection location is at
relatively high flue gas temperatures. This indicates that given droplet evaporation times on
the order of 50 to  100 msec, the main consideration is to be sure that the SNCR chemical is
injected and mixed upstream of the preferred "temperature window", typically 1700°F to
1850°F.
Cold Flow Modeling Tests

The ARIL lance ports at PSCC Arapahoe Unit 4 were existing ports, and there was not choice
in the location, so a cold flow modeling test was not performed.

For the PSNH Merrimack Unit 1 boiler, detailed cold flow modeling tests were conducted,
with six (6) possible ARIL lance locations, as shown in Figure 5.  It was initially thought that
Location 2, near the furnace roof, would provide the best results. Figure 6 shows tracer gas

-------
contours for the ARIL lances located at Position 2 (see Figure 5). The tracer gas contours
can be interpreted as local N/NO ratios assuming an overall N/NO ratio of unity. As can be
seen from the cold flow model tracer gas concentration profiles shown in Figure 6, the
mixing achieved at Location 2 averages only about 47% (i.e., the quantity M shown  in
Figures 6 and 7 is a statistically determined extent of mixing based on the tracer gas tests).
With the specified air compressors, the bottom half of the flue gas duct is basically not
covered with injection at Location 2. Further flow model testing was done to identify an
optimized location for the ARIL lances (i.e., Location 6).  As shown in Figure 7, the mixing
at 90 degrees (straight down) exceed 70%, an improvement of more than 50% in the mixing
for the same air compressor capacity.  This improvement makes the difference between
meeting and not meeting SNCR performance guarantees and could not have been predicted
without doing the flow model testing.
Installation Sequence

The ARIL lances are fabricated and assembled for testing in the shop. The assembly includes
a local PLC for automatic control of lance rotation angle as a function of boiler load, furnace
exit gas temperature (FEGT), or other preferred boiler operating parameter.  Each ARIL lance
includes a local operating panel, where the plant equipment operator can install or retract the
lance, and/or rotate it to any desired position within the operating envelope. The ARIL lances
are automatically retracted after a flush cycle in the event of (a) boiler load below a minimum
set point,  (b) loss of compressed air pressure, or (c) lance tip metal temperature are above a
preset limit.

Advanced lance metallurgy is required for long term operation in hot flue gas.  The selected
alloy is capable of short term (i.e., eight hours) operation at 2100°F.  At 1400°F, the selected
alloy is about 400 times stronger than 316 stainless steel  for resistance to thermal creep
effects, resulting in a lifetime expected to exceed three (3) years. Fortunately, the compressed
air cooling effect is greatest at the boiler sidewall location, where the bending moment is also
the greatest.  Lance deformation due to thermal creep effects has been estimated to be less
than 1.5 inches/year.

The ARIL lances were tested with compressed air and  water to confirm proper operation of
the system prior to shipping to the site.  A videotape of these tests, which includes some
details of  the cold flow model testing can be obtained from the authors.

The completed ARIL lance system is field-erected in the same way that new sootblowers
would be  installed. The required  connections for the compressed air and liquid piping are
made, and the electrical and control wiring connections are made. Startup testing includes
actuating  the ARIL lance system over its operating envelope of translation and rotation
functions.

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Status of Startup and Testing

At the time of the deadline for this paper, the PSCC Arapahoe Unit 4 ARIL lance system was
being started up, but no SNCR performance data had yet been obtained.  It is believed that
some data will be provided at the conference.

The startup of the PSNH Merrimack Unit 1 ARIL lance system is scheduled to begin in the
middle of May, 1995, with SNCR performance data to be available about the first part of
June, 1995. Please contact the authors for further information.
Capital Costs

The ARIL lance retrofit for PSCC Arapahoe Unit 4 (100 MW) was budgeted to be somewhat
less than $4.00/kW, including field installation by PSCC, including control system
modifications and startup testing, but not including about five weeks of performance testing.
The existing air compressor system and liquid chemical injection system was used at
Arapahoe Unit 4, and these items are not included in the price.  The project was started in
July, 1994, after the "stub" lance testing was completed.

The ARIL lance retrofit installation at PSNH Merrimack Unit 1 (120 MW) was budgeted to
be somewhat less than $15/kW, including all field testing, flow modeling, engineering design
and installation labor, equipment building, chemical storage tanks and forwarding pumps, 3 x
50% air compressors, 2 x 100% injection pumps, connection piping and wiring, ARIL lances,
centralized PLC control system and software, plus startup and initial system testing. The
project was started in September, 1994, and the initial field testing of the "stub" lances was
completed in October, 1994.

Due to the economy of scale that can be realized when ARIL lances are adapted to larger
units, a more realistic capital cost in the range from about $7/kW to about $10/kW could be
expected for boilers in the  size range from about 250 MW to about 750 MW.

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SOUTH
                GAS
                FLOW
NORTH
             Location for
             ARIL Lances
                                             SECONDARY
                                            SUPERHEATER
                                                                Full Load
                                                               Wall Injectors
                                Figure 1
                SNCR Injection Locations at PSCC Arapahoe 4

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co
1
rx
o
      10 -
                      67.5       56        45        33        22
                        Angle of Injection (degrees up from vertical)
18
                                          Figure 2
       Effect of Injection Angle for Proof-of-Concept SNCR Lance Tests at PSCC Arapahoe 4
                                  (Load: 60 MW, NSR - 1.0)
                    110 MWe, Lower Level
                    100 MWe, Lower Level
                    80 MWe, Lower Level
                    60 MWe, Lower Level
                    60 MWe, Lance
                                   20         30          40
                                        NO Removal (%)
                                          Figure 3
                   Proof-of-Concept SNCR Lance Results at PSCC Arapahoe 4

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                              Untreated Flue Gas
Injection Angle "StubTance
                         Passes Over Top of Test Lance
                                    40 :
                            Percent 30
                            DeNOx 20 !
                                    10
                    Figure 4
Proof-of-Concept Lance Tests at PSNH Merrimack Unit 1
   (Load: 120 MW, NOri = 900 ppm, NH^O, = 1.5)

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          Injection Lance
            Locations
45
        >'
       90
                                                                   Economizer
                                                                      Exit
                                   Figure 5
           Injection and Measurement Locations, PSHN Merrimack Unit 1
                            (Cold Flow Model Tests)

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   90 Degrees




   M = 4456
              NORTH
        a.
  67.5  Degrees




  M =  49*
             NORTH
        b.
                       20.00-
                       15.00-
                       0.00
                         0.00      5.00      10.00      15.00     20.00     25.00
                       20.00-
                       15.00-
                       10.0O-
                                                        SOUTH
                                                                              SOUTH
                                          10.00      15.00     20.00     25.00
   45  Degrees




   M  =  47*



            NORTH










       C.
                       15.00-
10.00-
                        0.00-
                                     Figure 6
                                                       SOUTH
PSNH Merrimack Unit  1 Cold Flow Tracer Gas Contours (Injection Location 2)

-------
90 Degrees   NORTH

M =  7156
            a.
                        20.00-
                        15.00-
10.00-
                         5.00-
                         0.00
                                                       SOUTH
                                                            2ooo     25.00
67.5  Degrees  NQRTH

M  =  635?



            b.
                        20.00-
                                                       SOUTH
                                   5.00      10.00      15.00     20.00     25.00
 112.5 Degrees NORTH

 M = 4756
             C.
                         15.00-
10.00-
                         5.00-
                         O.OO-
                                                       SOUTH
                           0.00       5.00      10.00     15.00      20.00     25.00
                                           Figure 7
      PSNH Menimack Unit 1 Cold Flow Tracer Gas Contours  (Injection Location 6)

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            INTEGRATED NOX CONTROL AT NEW ENGLAND POWER,
                            SALEM HARBOR STATION
                        M.B. Frish, S.A. Johnson, and J.P. Comer
                          PSI Environmental Instruments Corp.
                            20 New England Business Center
                                 Andover, MA 01810

                                         and

                               R.F. Afonso and A. Sload
                            New England Power Service Co.
                                  25 Research Drive
                               Westborough, MA 01582
Abstract

Selective non-catalytic reduction (SNCR) is a viable technology for reducing NOX emissions from
coal-fired boilers, especially those older units where large capital expenditures for alternative
technologies may not be justified. However, NOX reduction efficiency of the SNCR process is
maximized when the proper amount of reagent is injected at the proper temperature and dispersed
rapidly enough to avoid ammonia slip.

Early NEP experience at Salem Harbor station indicated that NOX reductions  of 60% were
achievable with SNCR. However, less NOX reductions were tolerated to avoid NH3 slip and
subsequent flyash contamination and visible stack plume resulting from excess ammonia.

Preliminary tests by PSI Environmental showed that ammonia slip could be monitored in real time
using their patented SpectraScan™-NH3 instrument, and that furnace exit temperature could be
continuously monitored and controlled using GasTemp™ another PSI Environmental product.
Based on this information, detailed tests were planned to show integrated control over the SNCR
process.  A goal of the project was to achieve lower NOX with less reagent! This paper describes
the status of the project.

Background of Project

In 1992, New England Power Company (NEP), and the Massachusetts Department of
Environmental Protection (DEP) reached an agreement that provided the basis for an innovative
demonstration project targeted to reduce nitrogen oxides (NOX) emissions from Units #1, #2,
and #3 at Salem Harbor Station. The agreement called for the application and demonstration of
Selective Non-Catalytic Reduction (SNCR). The agreement also included the potential

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application of a second technology, low-NOx burners, based on the success of the SNCR
demonstration.

SNCR is a technology in which a reagent such as urea or ammonia is injected in the upper part of
the boiler. The reagent reacts with NOX created by fuel combustion, converting it to harmless
nitrogen and water.

The SNCR demonstration involved two major efforts: 1) installing reagent (urea) injection ports
in the upper part of the boiler along with associated systems to control and monitor reagent flow;
and 2) optimizing the performance of the SNCR equipment which included a monitoring and
testing program with comprehensive instrumentation throughout the boiler.  The boiler of Unit #2
was selected for initial testing.  The SNCR supplier and an independent test contractor combined
to fully explore system performance for a variety of test conditions.

Preliminary Test Results

Spectrum Diagnostix, Inc. (SDx - formerly PSI Environmental Instruments Corp.) tested a pre-
commercial version of its SpectraScan™ ammonia monitor at Salem Harbor Unit #2 in 1994. The
purpose of the test was to prove the accuracy and response time of the instrument while gaining
experience necessary to improve the commercial design. Figure 1 shows ammonia content of the
flue gas measured by SpectraScan™ as compared to the value calculated from wet chemical
analysis of a flue gas grab sample taken at the economizer outlet.  In the latter case, flue gas
ammonia was absorbed in a known volume of dilute sulfuric acid and analyzed by ion-specific
electrode. Several  grab samples were taken at each sampling time to increase the accuracy of the
wet chemical method.
                                                           SNCR System
                                                             Shutdown
10-

 5-

 0
  SpectraScan
Calibration Check
      I
                           30
                      60         90
                          Time (min)
                                        Figure 1
        Ammonia Slip Measurements on SNCR System (High Sulfur Coal, Utility Boiler)

-------
It can be seen that SpectraScan™ was both accurate and responsive. Over a range of 6 to 34 ppm
of ammonia, SpectraScan™ was consistently within a ppm of the reference method value.  More
importantly, the instrument revealed the time duration of significant ammonia spikes that could
affect operation of downstream equipment.

Ammonia slip is not always so variable; the data in Figure 1 were taken during initial shakedown
of the SNCR equipment.  Figure 2 shows a more typical situation at another coal-fired boiler.
Here ammonia emissions are much more constant  at 2 to 4 ppm until the time when an additional
set of urea injectors was activated for a few minutes at 12:00 noon.  SpectraScan™ recorded a
spike of ammonia in the flue gas that reached about 65 ppm and then subsided when the urea was
turned off. Instrument response to this process upset was less than one minute. An unintentional
ammonia spike occurred later the same day as operators adjusted the system to operate at one-
third load.
      100
2 80
co
CO
E 60
Q.
     H 40
     o
     E
       20
                                •Steam Flow-
                                 FEGT	
                                 NH3-
                                                I
                                                             350
                                 280 ^
                                     ^
                                     ii
                                 210 *
                                     1
                                 140 "-
                                     ca
                                     cu
                                 70  co
        10:00
                12:00
 14:00
Time (h)
16:00
18:00
3000

2500

2000 \T
     o

1500 S
     a.

1000

0

  G-9369
                                         Figure 2
                     Ammonia Monitor Response to Spikes in Urea Flow
The initial tests at Salem Harbor provided insight into SNCR operation and revealed opportunities
for more precise process control.  Table 1 shows steady-state ammonia slip measurements
averaged over several hours of operation at constant boiler load. First, note the ammonia slip can
be quite variable even though boiler load may be constant. The ammonia concentrations are
shown to within ±1 standard deviation.  Comparing February 17th against February 23rd,
ammonia slip was quite different even when boiler loads were the same. A slight difference in flue
gas temperature leaving the air preheater hints that differences in furnace temperature may be
responsible for an increase in ammonia slip. As expected, increasing urea flow from a normalized
stoichiometric ratio (NSR) of 1.3 to 2.0 increased ammonia slip to unacceptable levels. Also,
ammonia slip could be minimized at low load as well as high load.

-------
                                        Table 1
               Ammonia Slip Measurements at Salem Harbor #2 - Steady State

Load, MW
Flue Gas O2, %
Air Heater Outlet
Ammonia at Econ
North
South
T, °F North
South
. Outlet, ppm
Normalized Stoichiometric
Ratio (estimated based on
expected NOX)
17 Feb 1994
83
3.8
3.1
265
278
2.1 ±1.4
1.3
18 Feb 1994
84
3.8
3.4
263
284
37.2 ±17.1
2.0
22 Feb 1994
38
7.7
7.5
255
255
10.3 ±5.0
1.3
23 Feb 1994
83
3.6
3.2
265
262
13.3 ±3.3
1.3
However, ammonia slip becomes very difficult to control during load swings. Table 2 shows a
steady increase in ammonia emissions as the Salem Harbor unit was ramped down to 38 MW
(about 45% of maximum rated capacity). During this test, urea flow was held constant during the
load transient and then adjusted to the proper NSR after low load was stabilized. The high
ammonia values underscore the need to match urea flow to NOX emissions as well as shift injector
location to follow temperature changes to prevent  ammonia slip during load swings. Note also
that ammonia concentrations decreased after the tubular air heater, indicating that ammonium
bisulfate may have deposited during this transient.  Higher NH3 at the air heater outlet at the end
of the load swing could indicate some offgassing from the deposits even after the ammonia slip
had stabilized.
                                        Table 2
         Ammonia Slip Measurements at Salem Harbor #2 - During a Load Reduction

Load, MW
Urea Flow, GPH
Injector Location
Air Heater Outlet T, °F North
South
NH3, PPM, @ Economizer Outlet
NH3, PPM, @ Air Heater Outlet
10:20 a.m.
66
202
Upper
260
262
66
25
11:30 a.m.
45
200
Upper
N/A
N/A
104
47
1:50 p.m.
38
213
Upper
255
255
47
91
2:55 p.m.
38
55
Lower
255
255
10
19

-------
Transient ammonia slip can be a real problem when SNCR is applied to cycling boilers. Figure 3
shows a 3-hour period of ammonia measurements at another coal-fired boiler. During this time
period, load ramped from 40 to 70% in the first hour, dropped back down to 40% in the second
hour, and ramped back up to 65% in the third hour. Ammonia slip held steady between 2 and
10 ppm, except for two spikes of about 40 ppm ammonia when load came up to 50%. This load
corresponds to point when the SNCR system sifts from a lower to upper level of injectors. Even
though ammonia quickly stabilized, spikes such as illustrated in Figure 3, if frequent enough,
could lead to equipment plugging or boiler operation problems.

E
Q.
a.
Q.
co
1C



100
80

60

40

20
0
	 Load
MH
Nrlg
-
-
___^'— **
- — x
M
J \
,
JI3:04
50% Load
;
-
-
^--•^""^•^^ s~-^. -
"** — 	 — -s__ x —
^\_s 	 '"""" A
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|V_^_;
,',,,,"
100
80

60

40

20
0



. — .
o^
CB
O


13:44 14:24 J15:04 15:44 Current
Time (h) '
cno/ ^ 50% Load
50% Load c-9241
                                        Figure 3
                         Ammonia Slip vs Load for a Cycling Boiler

Preliminary measurements with a continuous optical temperature monitor at Salem Harbor
indicated that changes in furnace temperatures can also limit the effectiveness of SNCR systems.
Figure 4 shows several hours of full load furnace exit gas temperature (FEGT) data at Salem
Harbor. The coal being burned on this particular day produced fluffy ash deposits on boiler
waterwalls above the burner zone. These deposits impeded heat transfer resulting in higher
FEGT.  When sootblowers were used to remove the ash deposits, FEGT decreased immediately
by 50 to 150°F; the magnitude of the temperature change depended on how many sootblowers
were used and the amount of ash removed at different locations in the boiler.

Two important conclusions relative to SNCR operation can be derived from these temperature
data:

1.     Reagent injection temperature is far from constant at constant load

2.     sootblowers (or burner tilts, burner tuning, etc.) can be used to hold injection temperature
       more nearly constant.

-------
               2700
               2600
               2500
             Q.
               2400
                2300
                                               _L
                                      J_
16.5      17.5      18.5      19.5      20.5
                         Time (24 h)
                                                                + Blow Soot
                                                                 21.5      22.5

                                                                          B-6791
                                        Figure 4
                              FEGT Data from Salem Harbor
SNCR Optimization
Current SNCR systems use a combination of open loop look-up table type and closed loop feed-
back control systems to choose the location and amount of reagent to inject in order to control
NOX emissions. These system typically monitor stack NOX and adjust total reagent flow to
maintain compliance; this is the closed loop portion. The injection location is chosen from several
possibilities using a look-up table which correlates unit load and pulverizers in service with the
location of the optimum temperature for reagent injection.  This look-up table can be significantly
in error depending on fuel properties and furnace cleanliness among other things.  Also, because
there is no direct indication of reagent utilization, significant amounts of ammonia slip (a result of
incomplete reagent utilization) can occur without the operator's knowledge. Ammonia slip can
cause operational problems such as air heater pluggage as well as economic penalties such as
wasted reagent and unsalable flyash. The current control system could be improved by the
addition of a direct injection location gas temperature reading and a continuous, real-time,
ammonia slip measurement.

In late 1994, NEP and SDx initiated a test program to demonstrate the feasibility of this new
SNCR control philosophy. The SDx SpectraTemp™ optical temperature monitor was chosen to
determine temperature in the injection zone. A pre-commercial SpectraScan® ammonia monitor
was installed at the economizer outlet.  Data from both these instruments can be analyzed along
with CEM and control room data to show possible savings brought about by  tighter process
control.
The tests are being conducted at Unit #2 at Salem Harbor Station. A sectional sideview sketch of
the unit is shown on Figure 5. Unit #2 is an 85-MW, single wall-fired boiler commissioned in
1952. It is equipped with B&W circular burners and a urea injection system for NO  control.

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                                                              -REHEAT INLET
                                                               HEADER
                                                              INTERMEDIATE
                                                                HEADER
                                         Figure 5
                                     Salem Harbor #2

The test plan includes three test series:

1.     baseline measurements
2.     parametric variations
3.     process optimization

During baseline testing, the SpectraTemp™ and SpectraScan® instruments were operated for
several weeks to show that the instruments are accurate and reliable, ammonia measurements
compared favorably against wet chemistry analysis as they had last winter.  During this time,
boiler and process operating data were collected to provide as basis for evaluating process
improvements.

Parametric tests are expected to take about one week to complete. Both boiler and SNCR
process variables will be changed systematically to measure the effects on furnace temperatures
and ammonia slip. A test matrix is shown in Table 3. Control room data taken at the beginning
and end of each test period include: load,  steam flow and temperature, flue gas 02 concentration,
pulverizer parameters (amps, airflow, inlet/outlet temperatures), attemperation spray flow or valve
position, urea flow rates to each injector,  and CEM data (NOX, O2, CO, opacity). For each test,
NSR will be varied in increments of 0.25 and held for about one hour while data are being
collected.

-------
                                         Table 3
                                  Parametric Test Matrix
Test No.
1
2
3
4
5
6
7
8
9
10
11
Load %
>90
>90
>90
>90
>90
<75
<75
<75
<75
<50
<50
Top Row
of Burners
Yes
Yes
Yes
Yes
No
Yes
Yes
No
No
Yes
No
Injectors
Upper
Upper & Middle
Upper
Upper & Middle
Upper & Middle
Lower
Lower & Middle
Lower & Middle
Lower
Lower
Lower
NSR
Min.
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
Max.
1.75
1.75
1.75
1.75
1.75
1.75
1.75
1.75
1.75
1.75
1.75
Furnace
Conditions
Dirty
Dirty
Clean
Clean
Clean
As found
As found
As found
As found
As found
As found
For the process optimization tests, the instruments will be used to maintain desired injection
temperatures and ammonia slip over the normal range of unit load. First, the sootblower schedule
will be modified if necessary to better maintain the injection temperatures shown to minimize NOX
and ammonia slips.  Then, if NH3 is below 5 ppm, urea flow will be increased to achieve even
lower NOX.  If NH3 is above 5 ppm, urea flow will be decreased to reduce NH3. At reduced
loads or when mills are out of service, injector locations will be changed according to changes in
measured temperatures. The results of these tests can be used by NEP, SDx, and the SNCR
system supplier to engineer an improved control subsystem.

Project Status

As of this writing, the baseline tests are in progress.  The SpectraTemp™  instrument and the
electronics console of the ammonia monitor have operated unattended and trouble-free for three
months.  The NH3 measurement cell and gas extraction probe have experienced periodic
problems, but have been operating successfully for the last three weeks.

The sampling cell operates at  about 0.3 atm pressure to increase accuracy of the measurement,
and above 500°F to assure that all ammonia is in the gas phase. This high temperature, low
pressure environment has been a challenge to all seals. O-ring seals have been upgraded to
Kalrez® to assure temperature resistance.  Also, all constricted flow passages (filter, pressure
reducer, etc.) have been relocated inside the probe where they are heated internally by rod heaters
and externally by the hot flue gas.  Cold spots that could cause consideration of ammonium
bisulfate aerosol that plug the  sample line at these flow restrictions are thus avoided.

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Figure 6 shows an example of continuous ammonia measurement made at Salem Harbor #2
during a 24-hour period on 9 April 1995. In this plot, the continuous measurements were
converted to rolling 2-minute averages by the data reduction program. Unit #2 normally cycles
between full load and control load depending on the demand for electricity. It is interesting to
note that the times when ammonia slip exceeds 10 ppm corresponds to when the boiler is not at
full load. Work to achieve more quantitative correlation of ammonia with boiler operation is now
in progress.
                    60
                 -o
                 CD
                    50
                    40
                 a
                 
-------
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


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                         Figure 2
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-------
                   FigureS
    Process Flow Diagram of SNCR System
Circulation Pump
                                      Distribution
                                       Modules
        Figure 4, Montaup Electric
                     Full Load
             NH3 slip vs NOX Reduction
                                                          Each Zone
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-------
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-------
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-------
        Figure 9, Montaup Electric
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             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).

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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

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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)

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-------
     4000
     3000 -
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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)

-------
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                                                                                                         Preheat
                                                              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
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 D)
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      3000
      2500  -
2000 -
1500 -
      1000  •
       500  -
                   10
                                                    50
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       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

-------
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       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

-------
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                  10
                     20       30       40
                    Exposure Time, minutes
                                                       50
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                                      Figure?
                  Port Jefferson Oil Ash NH3 Absorption as a Function of
                            Exposure Time and Temperature
 E
 Q.
 Q.
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      200 -
      150 -
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                  10
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                                                       50
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                                      Figure 8
                   Rochester Coal Ash NH3 Absorption as a Function of
                            Exposure Time and Temperature

-------
     I
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                      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
£
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-------
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
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     200
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                     time


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                                                     °0
        7.0
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9.0
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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.

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  CD




  O
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       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
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          1500
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 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

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            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 -

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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-

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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-

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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-

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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-

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                                  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-

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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-

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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-

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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-

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                 Page -17-

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                              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

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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

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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;

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     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.

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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.

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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).

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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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Fig. 5  -  AEM CASSANO UNIT  #j  - NEW  GAS REBURNING SYSTEM

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      8
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           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.

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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.

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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.

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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%.

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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).

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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).

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c
 PRIMARY
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                                        NOX -40%
                                       BURNOUT
                                         ZONE
                                     Normal Excess Air
                              Figure 1
                         The Rebuming Process
                                                     |NOX -40%
                                                      -60% NOX
                                                      Reduction
  PRIMARY
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                              Figure 2
                    The Advanced Rebuming (AR) Process
                                    NOX~15%
                                                      -85% NOX
                                                      Reduction

-------
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-------
N20 (ppm)
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                                                 Sodium
                                                 Promoter
10
               0
               1400
                   1600              1800
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                                   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

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   SNCR
   Agent
 Reburning
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                                                 Baseline
                                                Reburning
                                               SNCR agent
    NOx
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                                    Figure 7
                     Advanced Reburning (AR) Without Synergism
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-------
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-------
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                    Multiple Injection Advanced Reburning (MIAR)

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      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.

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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.

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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.

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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.

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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

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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

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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

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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.

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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.

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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.

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     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.

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 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.

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              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

-------
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

1.     U.S.  Department of Energy.  Office of Fossil Energy.  Enhancing the Use of Coals by
       Gas Rebuming and Sorbent Injection; A Project Proposed by Energy  and
       Environmental Research Corporation. Washington, D.C.:  Government Printing
       Office, May 1987.   DOE/FE-0087 CCT/87 PC 79796.
2.     U.S.  Department of Energy.  Office of Fossil Energy.  Evaluation of Gas Rebuming
       and Low NO,. Burners on a Wall-Fired Boiler. Washington, D.C.:  Government
       Printing Office,  September 1990. DOE/FE-0204P.
3.     W. Bartok and BA. Folsom, "Control of NOX and SO2 Emissions by Gas Reburning-
       Sorbent Injection,"  presented at the American Institute of Chemical Engineers Annual
       Meeting, New York, New York  (November 1987).
4.     R. Payne et. al., "Demonstration of Gas Reburning-Sorbent Injection NOX/SO2 Control
       Technology on Three Utility Boilers," presented at the American Institute of Chemical
       Engineers  1988  Summer National Meeting, Denver, Colorado (August 21-24,  1988).
5.     K. T. Wu, et. al., "Development and Application of a Gas Rebuming Process Model
       for the Design of Boiler NOx Reductions," presented  at the 1991 International Joint
       Power generation Conference, San Diego, California (October 1991).
6.     B. A. Folsom and W. Bartok, "Gas Rebuming - Sorbent Injection for the Control of
       Acid Rain Precursors from Coal Fired Utility Boilers," presented at the ASTM
       Symposium on Innovations  and  Uses for Lime, San Francisco, California (June 19,
       1990).
7.     R. T. Keen, et. al, "Gas Rebuming -Sorbent Injection Demonstration Results,"
       presented at the 1993 EPRI/EPA/DOE SO2 Control Symposium, Boston,
       Massachusetts (August 24-27, 1993).
8.     B. A. Folsom and M. Browning-Sletten, "Evaluation of Gas Rebuming and Low NOX
       Burners on a Wall Fired Boiler," presented at the ASME International Joint Power
       Generation Conference, Boston,  Massachusetts (October 21-25,  1990).
9.     L. C. Angello et. al., "Gas Reburning-Sorbent Injection Demonstration Results,"
       presented at the U.S. Department of Energy First Annual Clean Coal Technology
       Conference, Cleveland,  Ohio (September 22-24, 1992).
10.    T. M. Sommer,  et. al., "Integrating Gas Rebuming with Low NOX Burners,"  presented
       at the U.S. Department  of Energy First Annual Clean Coal Technology Conference,
       Cleveland, Ohio (September 22-24,  1992).
11.    A. Sanyal  et. al., "Cost Effective Technologies for SO2 and NOX Control," presented  at
       Power-Gen '92,  Orlando, Florida (November 17-19, 1992).
12.    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

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       Symposium on Stationary Combustion NOX Control, Miami Beach, Florida (May 24-
       27, 1993).
13.    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).
14.    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).
15.    A. Sanyal et. al., "Advanced NOX Control Technologies," presented at the Tenth
       Annual International Pittsburgh Coal Conference (September 20-24, 1993).
16.    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).
17.    T. J. May, "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 (September 6-8, 1994).
18     U.K.  Patent Office.  Process for Disposed  of Oxides of Nitrogen. Robert D. Reed,
       John  Zink  Company.  U.K.  Patent No. 1,274.637, 1970.
19.    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).
20.    Y. Takahashi et al., "Development of  Mitsubishi MACT In-Furnace NO, Removal
       Process,"  presented at the U.S.  Japan NOX Information Exchange, Tokyo, Japan
       (May 25-30,  1981).
21.    Y. Takahashi, et. al., "Development of 'MACT' In-Furnace  NOX Removal Process for
       Steam Generators,"  presented at the 1982  Joint EPA/EPRI Symposium on Stationary
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22.    S. B. Greene et. al., "Bench Scale Process Evaluation of Reburning and Sorbent
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       Through the Supplemental Use of Natural Gas," Final Report, GRI 5083-251-0905,
       1985.
24.    J. Pont. et. al. Glass Tank NOX Emission Control with Gas Reburn. GRI Report No.
       GRI-94/0018.2. March,  1994.
25.    D. K. Moyeda et. al., "Application of  Gas Reburning Technology to Glass Furnaces
       for NOX Emission Control,", presented at the AFRC/JFRC Pacific Rim International
       Conference on Environmental Control of Combustion Processes, Maui, hawaii
       (October 16-20, 1994).

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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

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       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

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                                      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

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   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

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   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

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   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

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   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

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              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.

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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,

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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

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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

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    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

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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.

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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.

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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











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                   +  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.

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                      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

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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

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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.

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GAS OUTLET   STEAM COIL
          "AIR HEATER
        Figure 7 - Eastman Kodak Company's Boiler No. 43

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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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