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BR 1834 PDF
BR 1834 PDF
BR-1834
Authors:
J. Pham
Babcock & Wilcox Canada
Cambridge, Ontario, Canada
D. Wasyluk
Babcock & Wilcox
Power Generation Group, Inc.
Barberton, Ohio, U.S.A.
W. Small
Nova Scotia Power
Halifax, Nova Scotia, Canada
Presented to:
2009 Power-Gen International
Conference
Date:
December 8-10, 2009
Location:
Las Vegas, NV, U.S.A.
D. Wasyluk
Babcock & Wilcox
Power Generation Group, Inc.
Barberton, Ohio, U.S.A.
Presented to:
2009 Power-Gen International Conference
December 8-10, 2009
Las Vegas, NV, U.S.A.
W. Small
Nova Scotia Power
Halifax, Nova Scotia, Canada
BR-1834
Abstract
Nova Scotia Power Incorporated (NSPI) operates four
coal-fired generating stations supplying about half of the
provinces electricity needs. Nitrogen oxides (NOx) from
the stations had increased with both higher thermal generating load and petroleum coke blending as major contributors
since 2000. NSPI began assessing options to reduce NOx
emissions in 2005 and embarked on a multi-phase plan to
reduce overall NOx emissions by at least 40%. This paper
addresses strategic planning, design considerations, and
performance test results of the separated overfire air (SOFA)
NOx reduction program at the Lingan Generating Station.
Introduction
Nova Scotia Power is a vertically integrated, regulated
subsidiary of Halifax-based Emera Inc. which owns and
operates most of the electricity generation for the province
of Nova Scotia in Atlantic Canada. The generation is a mix
of renewable and fossil fuels totalling 2293MWe. Renewable energy sources include 33 small hydroelectric plants
on six rivers, two wind turbines, and one tidal plant. The
rest of the generation capacity is thermal which includes a
183MW circulating fluidized bed (CFB) unit at Point Aconi;
four 160MW tangentially fired units at Lingan; two 185MW
wall fired units at Trenton; a 155MW tangentially fired unit
at Point Tupper; and seven single-cycle combustion turbines.
The thermal plants are fuelled by coal and petroleum coke
while the combustion turbines burn oil and natural gas.
Since 2005, Nova Scotia Power has developed a strategy
for sustainable reductions in emissions including greenhouse gases. The plan focuses on three priorities: increase
generation from renewable sources, take a leadership role
Babcock & Wilcox Power Generation Group
Although the kinetics involved in the conversion of organically bound nitrogen compounds found in fossil fuels
are not yet fully understood, numerous investigations (Habelt
& Howell 1976, Habelt 1977, Pershing & Wendt 1976, Pohl
& Sarofim 1976) have shown that the major source of NOx
emissions is nitrogen bearing fuels such as coal and oil.
Although there is little doubt that fuel bound nitrogen is an
important contributor in the formation of NOx, the mechanism involved in the transformation of fuel bound nitrogen
to NO is very complex. It appears that the majority of the
fuel NOx formation occurs by two separate paths. The first
involves the oxidization of volatile nitrogen species during
the initial phase of combustion. During the release, and
prior to the oxidization of the volatile compounds, nitrogen
reacts to form several intermediate compounds in the fuel
rich flame regions. These intermediate compounds are then
oxidized to NO or reduced to N2 in the post-combustion
zone. The formation of either NO or N2 is strongly dependent on the local fuel/air stoichiometric ratio. The second
reaction path involves the release of nitrogen radicals during
combustion of the char fraction of the fuel. These reactions
occur much more slowly than the reactions involving the
volatile species. These investigators have made quantitative measurements in laboratory scale, tests conducted by
Habelt (1977), burning fuel oil in a mixture of oxygen and
carbon dioxide, which has shown a remarkable correlation
between the percentage of nitrogen in the fuel and NOx
formation. However, similar tests run for various coals
have not produced similar results. Clearly, the coal test burn
results indicate that the fuel-nitrogen conversion rate is not
constant, but varies widely depending more on coal rank
than on actual nitrogen content. Pershing and Wendt (1976)
further isolated fuel NOx by burning coal in a synthetic oxidant mixture that has a specific heat similar to air, however,
containing no nitrogen: the mixture consists of 21 percent
oxygen, 19 percent carbon dioxide, and 61 percent argon.
On the basis of four different coals, the studies showed that
the fuel NOx, unlike thermal NOx, was relatively insensitive
to flame temperature.
bottom end air and one close-coupled OFA. The intermediate auxiliary air compartment had been decommissioned in
that the oil gun has been removed and the dampers locked
closed. The remaining two oil levels could achieve approximately 65% load or 100MWe.
Table 1
Bituminous Coal and Petroleum Coke Fuel Analysis
Unit 1
(2008)
80% Colombian
Units 2 & 4
(2007)
20% US
Appalachian
65% Venezuelan
Unit 3
(2006)
35% US
Appalachian
80% Colombian
20%
Petcoke
12.36
9.13
10.06
11.25
12.33
7.39
Ash
6.84
8.12
5.47
7.84
8.28
0.50
Fixed carbon
47.63
45.01
47.66
46.29
53.30
89.16
Volatile matter
35.47
35.62
34.54
38.48
38.42
10.34
HHV, Btu/lb
12044
12069
11807
12812
13126
15409
69.53
68.14
67.31
70.87
79.18
88.34
Hydrogen
4.76
4.70
4.61
4.93
5.52
3.61
Nitrogen
1.44
1.23
1.40
1.26
1.52
2.33
Oxygen
6.64
3.90
8.04
4.51
4.73
0.51
Sulfur
0.70
2.65
0.83
3.20
0.77
4.52
Moisture
10.06
11.25
12.33
7.39
12.36
9.13
Ash
6.84
8.12
5.47
7.84
8.28
0.50
Conclusion
References
1. De Soeto G. (1973). Mechanism of Nitric Oxide Formation from Ammonia and Amines in Hydrocarbon
Flames. Revue de Linstitut Francais du Petrole et
Annuales Des Combustible Liquides, 28(1):95-108.
2. Habelt W.W. (1977). The Influence of Coal Oxygen to
Coal Nitrogen Ratio on NOx Formation. Presented at
the 70th Annual AIChE Meeting, New York, November
13-17, 1977.
3. Habelt W.W., and B.W. Howell (1976). Control of NOx
Formation in Tangentially Coal-Fired Steam Generators. Proceedings of the NOx Control Technology Seminar, San Francisco, February 5-6, 1976. Special Report.
Report No. PB-253 661 (EPRI SR 39). Springfield, VA:
National Technical Information Service.
4. MacKinnon D.J. (1974). Nitric Oxide Formation at
High Temperature. Air Pollution Control Association
Journal, 24 (3): 237-239, March 1974.
5. Pershing D.W., and J.O.L. Wendt (1976). The Effects of
Coal Composition on Thermal and Fuel NOx Production from Pulverized Coal Combustion. Central States
Section. The Combustion Institute Spring Meeting,
Columbus, Ohio, April 4-6, 1976, Pittsburgh: The
Combustion Institute.
6. Pham J., and K. MacLean (2006). Design and Performance Characteristics of a Reburning System at Coleson Cove Generating Station. Presented at Power-Gen
International in Orlando, Florida, USA. November
28-30, 2006.
7. Pham J., and K. MacLean (2007). Successful Implementation of Multi-Stage Gas Emissions Reductions
at 1050MWe Coleson Cove Generating Station Using
Reburn, WFGD, and WESP Technologies. Presented
at Power-Gen International in New Orleans, USA.
December 11-13, 2007.
8. Pohl J.H., and A.F. Sarofim (1976). Devolatization
and Oxidization of Coal Nitrogen. 16th Symposium
on Combustion, Massachusetts Institute of Technology, Cambridge, Massachusetts. Pp. 491-501, August
15, 1976.
9. Sarofim A.F., and J.H. Pohl (1972). Kinetics of Nitric
Oxides Formation in Premixed Laminar Flames. Presented at the Fourteenth Symposium on Combustion,
Pennsylvania State University, University Park, Pennsylvania, August 20-25, 1972.
10. Zeldovich Ya. B. (1946). The Oxidation of Nitrogen
in Combustion and Explosions. Acta Physicochimica
U.S.S.R., 21:577-628.
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