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Effect of Ammonia Injection on NOx Emissions for a Recovery Boiler

Sunday, January 17th, 2010

For modern recovery boilers, which are designed for low NOx emissions, the conversion rate of N2 to NOx can be lower than 15-20%. The recovery boiler operating conditions such as excess air, furnace temperature and air staging have a direct effect on the emission rates [1]. Selective non-catalytic NOx reduction (SNCR) has been used in power boilers to reduce NOx emissions. This technology was borrowed for a series of tests on a 2000 tds/d recovery boiler built in 2001 by Metso Power, equipped with quaternary air [2]. The SNCR technology injects ammonia into the flue gas stream at a certain temperature range to reduce NOx into N2 gas.  Critical factors are good mixing and sufficient residence time at the right temperature. At too high a temperature, the ammonia oxidizes to NOx whereas, at low temperatures, the reactions are too slow and ammonia leaves the boiler un-reacted (ammonia slip).

A series of tests were carried out with ammonia injections, and the gas and deposit compositions were monitored extensively. The injection took place through lances, at three different injection levels, with air atomized spray nozzles. Carrier air was provided around each lance at the screen level to improve penetration in the furnace. At the lowest level, the quaternary air was used as carrier air. Long term tests at the quaternary level were carried out at 62% load while, at the injection level below the screen tubes, tests were conducted at 74% load or higher.

During the trials, FTIR was used for monitoring the emission composition. The flue gas temperature at the injection position was also measured.  Deposit probes were used in the superheater and economizer areas, with temperatures controlled at 450, 250 and 150 C. Based on the data obtained, a significant reduction in NOx emission was achieved (30-50%).  For other gaseous compounds, the CO emission did not change much, although it was difficult to operate the boiler under exactly controlled conditions.  Other species, such as SO2, HCl, HF and N2O were not clearly impacted by the addition of ammonia. In nine out of twelve tests the reduction in NO was followed by a reduction in NO2. Only in one case was there a significant increase in NO2 which was due to very low levels of NO2 in both cases, i.e., with and without the SNCR turned on. In this study, the ammonia slip was typically less than 20 ppm. A slip much higher than this cannot be tolerated, for environmental and economical reasons.

CFD simulations showed that the penetration of the SNCR jets into the recovery boiler gas steam was poor, indicating that a limited number of injection ports were not adequate to ensure an even distribution. This suggests that significant improvements to the injection system can be made.

The compositions of the ESP ash and deposits collected on the probes showed that ammonia injection had little impact on the properties of the ash. Thermodynamic calculations confirmed that ammonium salts would not form in the superheater region. The formation of liquid NH4HSO4 in the cooler part of the flue gas channel, for boilers with high SO2 emission, is a possibility. However, due to the significant amount of sodium present, most of the liquid salt will be in the form of NaHSO4 and the effect of NH4HSO4 is expected to be negligible.

References:
1.    Distribution of Black Liquor Nitrogen Between Smelt, NOx and Flue Gases in Recovery Boilers, K. Saviharju et al, TAPPI 2007 Chemical Recovery Conference, Quebec City, QC, Canada.

2.    Effect of Ammonia Injection on Black Liquor Recovery Boiler NOx Emissions and Ash Chemistry, M. Lundberg et al, TAPPI Engineering, Pulping & Environmental Conference, Aug. 24-27, 2008, Portland, Oregon, USA.



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NOx Emissions

Saturday, October 17th, 2009

One of the drawbacks in high solids firing is the increased rate of NOx emission. Since NOx contributes to acid rain formation, a reduction in its emission is desirable. To control NOx emissions, knowledge of nitrogen chemistry in the recovery cycle is required. A study of three European mills showed that about 95% of the N2 in wood is released during pulping, with 10-15% being converted to ammonia. The remaining nitrogen is in the form of organic compounds; these compounds, and about half of the ammonia, end up in the black liquor (BL) [1]. Char gasification tests indicate that most of the nitrogen in the char is converted to cyanate during char oxidation, and that about 30% of it ends up in the smelt. Cyanate reacts to form ammonia in alkaline solutions such as green and white liquors. This, in turn, is vented from the liquor storage tanks or returned to the digester with WL. The ammonia is then vented from the digester blow tank or the early evaporator’s effects. When BL is concentrated to about 30%, some additional ammonia and a small amount of volatile organics are released into the foul condensate.

A more recent study [2] of 18 European mills over six years of operation, with recovery boilers manufactured or retrofitted by Andritz, shows that nitrogen distribution in the recovery cycle can vary widely between different mills with different recovery boilers (RBs).  The conversion to NOx was about 12-46%, while the conversion into N2 varied between 40-77%; the amount of nitrogen in the smelt was 8-28%.  For modern RBs, the conversion of nitrogen to NOx was about 20-30% of the total nitrogen content of BL. For RBs which are designed for low NOx emission, the conversion can be lower than 15-20%.  For these RB’s, the breakdown was 15% into NOx, 10% into smelt and 75% into N2 in the flue gas.  These boilers operate in steady conditions, with continuously cleaned air port openings and liquor guns, and well controlled excess air. The flue gas NOx emission rates correlated with excess air, furnace temperature, air staging and, in some cases, with the amount of carryover.

Lower NOx emissions may increase SO2 emissions if sulfidity is high and the furnace hearth temperature is low. The operating conditions for low NOx emissions may lower the melting point of carryover, resulting in fouling and corrosion in the superheaters, lower power generation capacity and increased steam consumption for soot blowing.
For some boilers, the high carryover resulted in a lower concentration of nitrogen in the smelt. This is because char particles burning in the upper furnace produce NOx, reducing the amount of nitrogen in smelt.  High liquor loading and high reduction efficiencies also decreased the nitrogen content of smelt. NOx emission did not appear to be connected to the concentration of nitrogen in smelt.

According to the results of this study, the key factors affecting the conversion of nitrogen into NOx are: furnace loading, design of the air and liquor systems, excess oxygen in firing, liquor dry solids, droplet size and design of the NCG burners.  Both the lower and upper furnace zones affect the conversion of nitrogen into NOx. A 1% unit decrease in excess oxygen in flue gas would reduce the NOx emission by 20 ppm.  The flue gas temperature in the final oxidation area has a direct effect on the conversion factor.
The nitrogen in char in the lower furnace, under reducing conditions and high temperature, forms N2 instead of NOx.

References:

1.    Distribution and Release of Nitrogen Compounds at Kraft Pulp Mills-A Survey of Three European Mills, N. DeMartini et al, Tappi 2004 Chemical Recovery Conference, June 6-10, Charleston, SC, USA.
2.    Distribution of Black Liquor Nitrogen Between Smelt, NOx and Flue Gases in Recovery Boilers, K. Saviharju et al, Tappi 2007 Chemical Recovery Conference, May 29-June 1, Quebec City, QC, Canada.



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