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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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Modern Recovery Boilers

Sunday, April 5th, 2009

New recovery boilers are being installed around the world which are bigger, have higher efficiencies and produce more electricity. Producing green electricity for sale based on renewable resources has put a new focus on the recovery operation. About 80% of the 20 most recent recovery installations have higher pressures (>85 bar) and higher temperatures (>480o C). New recovery boilers have capacities of more than 5000 tds/day, with some evaporation units exceeding 1000 t H2O/h water removal capacity [1].

New recovery capacity is being built in Asia and South America, where half of the new mills produce HW pulp (Eucalyptus). Europe and North America account for less than half of total new recovery capacity. In Europe and North America, there are a lot of old recovery boilers, with an average age of 30 years. Since the life expectancy of a recovery boiler is about 30-40 years, significant investment in older mills is required within the next 10 years. The alternative is mill closure. Click to continue »



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Controlling Black Liquor Viscosity

Sunday, January 18th, 2009

The viscosity of black liquor affects its handling properties and is a critical parameter for the control of a recovery furnace, in terms of the spray characteristics and the char bed size and shape. Many mills have increased the as-fired black liquor solids in order to improve their boiler’s thermal efficiency, increase liquor throughput and reduce environmental emissions. However, black liquor viscosity increases significantly at solids concentrations over 70%. If a mill is not equipped with a pressurized liquor handling system, in which high temperatures can be used to reduce viscosity, another viscosity reduction method such as alkali profiling may have to be used to facilitate high solids firing. There are other methods to reduce viscosity, such as liquor heat treatment or high temperature oxidation, but these involve capital cost. For more information on black liquor viscosity see my posts of May 26, June 9 and June 28, 2007. Click to continue »



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SO2 emission dependency on recovery boiler operation

Sunday, November 16th, 2008

Modern recovery boilers (RB) operating at high bed temperatures have, typically, a low SO2 emission. These RBs have a modern air system and, by firing liquor at high solids concentrations, create adequate burning intensity and mixing in the lower furnace. Older boilers operating at high sulfidity, low dry solids and/or a not sufficient air system will have a high SO2 emission rate, i.e., around 1000 mg/Nm3 [1].

The molar ratio of S/Na in black liquor (BL), along with furnace operating conditions, determine the chemistry of the S and Na in the flue gas. Based on the results obtained from a flue gas survey of different boilers, the range for Na and S emissions has been examined. For RBs with a low S/Na ratio in the flue gas (high burning intensity) and a hot bed, more Na is released than needed to bind with S, resulting in little or no SO2 emission. The fly ash will contain a high Na2CO3 concentration, corresponding to a high pH. RBs with a high S/Na ratio in the flue gas have low burning intensity and colder beds that do not release enough Na to capture S, resulting in more SO2 emission and the formation of acidic sulfates, which lower the sticky point of the ash and its pH. Click to continue »



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Smelt Flow Problems

Sunday, January 6th, 2008

Many mills experience smelt flow problems, which could lead to dissolving tank explosions and plugged smelt spouts. Liquor chemistry affects the smelt composition, causing changes in the smelt melting point and its viscosity. Higher melting point smelts tend to have higher viscosity at a given temperature. The sulphide content of the smelt has the most significant effect on the smelt’s melting point. The melting point and viscosity decrease as the sulphidity increases to about 40%, but increase rapidly when the sulphidity increases over 40%. Also, when the boiler is operating at very high reduction efficiencies (i.e., low Na2SO4 content in the smelt) the smelt melting point increases significantly.  K and Cl enrichment reduces the smelt melting point and the viscosity. 

Other factors, such as boiler operating conditions and design may also have an effect. Smelt spout feed water temperatures below BLRBAC guidelines (60-65 oC) can result in low smelt temperatures and high viscosity, or in the solidification of smelt in the spouts. High furnace drafts, and excessive air infiltration around the smelt spouts, could also cool the smelt, with the same result.  

Incomplete combustion of the BL organics, or firing a highly viscous BL, could lead to high carbon content in the smelt, raising the smelt melting temperature and viscosity. This can be verified by measuring the suspended solids in the unclarified green liquor. If the suspended solids are over 1200 ppm, this is an indication of unburned carbon or a dregs related problem [1]. Increased BL viscosity can result in the formation of larger droplets, that fall closer to the walls and increase the carbon or dregs content of the smelt. Other factors influencing smelt flow include bed temperature, excessive metals build-up in the smelt, a change in chemical makeup, upsets or control problems with practices that add Cl to the system, and a change of furnish. 

1.  Karidio, I, et al, A review of the conditions in chemical recovery boilers that result in poor-flowing smelt, 2004 Int. Chem. Rec. Conf.



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Sintering of recovery boiler dust

Tuesday, December 11th, 2007

Tough-to-remove deposits can form on the surfaces of recovery boiler (RB) tubes, even when the flue gas temperatures are too low to melt the dust.  Deposits formed from fume particles can begin to sinter and harden around 300o C, and the rate of sintering increases significantly with temperature.  The sintering tendency is affected by the dust’s composition and physical properties, and the RB operating conditions. 

The composition of the fume particles changes as they move through the upper furnace, reacting with sulphur oxides. However, beyond the superheater region, the composition does not change very much (as the SO2 levels are low) and the composition of the fume that deposits on the boiler bank tubes is the same as the ESP dust. Research has shown that the chloride content of the dust has a direct effect on sintering [1]. At Cl levels of less than 2 mole % (Cl/(Na+K)), the dust does not sinter well.  The effect of K becomes significant when the Cl content is more than 2 mole %.  The combination of high Cl and high K increases the sintering rate significantly. This is to be expected, as NaCl and KCl have a high vapour pressure relative to the other components of the dust, and they also decrease the first melting point temperature (FMT).  Rapid sintering takes place when the FMT is lowered. The FMT of RB dust without any Cl is very high (780o C). However, this is greatly reduced (<600o C) if a small amount of Cl is present. The FMT of dusts containing Cl will be affected mainly by K and, to a lower extent, by carbonate. Of the dust’s physical properties, an increase in un-compacted bulk density results in reduced sintering. This means that light dusts sinter more, while more dense dust (i.e., from the ash hopper) sinter less. The dust composition and particle size can be affected by the boiler’s operating conditions.  High solids firing, and increasing the firing load, result in hot beds and a low SO2 concentration in the flue gas. The light dust will contain more carbonate and Cl, and sinter more readily. 

SO2 at 1.0% concentration has been found to have a major impact, greatly increase the rate of sintering [2]. Since high levels of SO2 are not usually found in RB in the superheater section and beyond, SO2 is not usually a factor in the sintering of deposits. However, during upset conditions (i.e., a cold char bed) when the SO2 concentration is increased for a short time, sintering conditions are favoured.

 1.             The sintering tendency of recovery boiler precipitator dust, Duhamel, M., et al, 2002 Tappi Fall Conf. & Trade Fair

2.             Effect of gas composition on fume sintering rates, Lien, S.J., et al, 2004 Int. Chem. Rec. Conf.



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Plugging of kraft recovery boilers

Sunday, November 18th, 2007

Plugging problems in kraft recovery boilers (RB) are caused by a combination of factors. These are: the particle quantity, particle composition (e.g., stickiness), recovery boiler operating conditions and sootblowing efficiency.  The concentration of soluble elements such as Cl and K increases in the recovery cycle when mills reduce water consumption and liquor losses, and/or recycle bleaching effluent.  Cl and K lower the melting point and decrease the sticky temperature of the deposits formed on the tube surfaces.  Deposits include carryover (0.01-3 mm), fume (0.1-1 ?m) and intermediate size particle [1]. 

Carryover particles are partially oxidized smelt or partially burnt black liquor (BL) droplets, and they deposit mostly on the superheater tubes. Fume particles form by condensation of the vapours of Na/K compounds, and mostly deposit on the generating bank and economizer tubes.  The quantity of carryover particles increases when the firing load is increased, when the proportion of smaller liquor droplets increases (i.e., from firing low viscosity liquors), and when the flue gas velocity is high. The quantity of fume particles is determined by the vapourization rate of Na/K compounds from the char bed, and the rate of Na/K release during liquor pyrolysis.  Therefore, operating the boiler with a hot bed (i.e., high solids firing) will generate more fumes in the upper furnace. High solids firing will also produce larger droplets, lower the quantity of particles and reduce fouling by carryover.  

The particles formed in the RB have to be sticky to adhere to the tube surfaces. The stickiness of the particles depends on their liquid content when they impact the tube surface. The liquid content depends on the particle composition and temperature. It has been shown that particles with a liquid content of over 15% are sticky. The sticky temperature can be estimated if the particle’s composition is known [2]. However, this is not usually possible, as the composition changes continuously when carryover particles are being formed and deposited.  Laboratory and field tests indicate that the Cl content of carryover particles is around 30% of the Cl in the feed BL, and the K content is about 80% that of the feed BL [3].  Two factors appear to be responsible for the depletion of Cl in the carryover with time: one is the vapourization of Na/KCl, and the other is the sulphation of Na/KCl by SO2 in the flue gas, that releases HCl.  

2Na/KCl +SO2+O2+H2OàK2/Na2SO4+2HCl? 

Higher bed temperature leads to greater depletion of Cl and K, higher sticky temperatures and reduced deposition of carryover. However, greater depletion of Cl and K in carryover leads to greater enrichment of these elements in the fume.  Field studies have shown that there is a linear correlation between the K and Cl contents of the as-fired BL, the smelt, the carryover deposits and the ESP dust [3]. This linear correlation is not expected to hold if there is excess sulphur in the flue gas. Simple approximation can be used to estimate the composition and sticky temperature of carryover in a RB. This approximation is based on the above- mentioned linear relationship. Chemical analysis of the as-fired BL and ESP dust is all that is required for the calculation of the sticky temperature. First of all, Cl and K enrichment factors are calculated for the ESP dust.  The enrichment factor for Cl can then be plotted versus that of K. The linear graph is extrapolated to estimate the Cl and K content in the carryover, using a Cl enrichment factor of about 0.4 and a K enrichment factor of about 0.88 [3]. The sticky temperature can then be predicted for a range of carryover, using available graphical data [2].

1.                   Tran, H.N. et al, Fouling of tube surfaces in kraft recovery boilers, 40th anniversary, Int. Rec. boilers conf., Porvoo, Finland. March 12-14 (2004).

2.                   Tran, H.N. et al, The sticky temperature of recovery boiler fireside deposits, Pulp & Paper Canada, 103:9, P.29-33 (2002).

3.                   Khalaj, A. et al, Composition of carry over particles in recovery boilers, Chem. Rec. Conf. Charleston, SC, USA, June 6-10 (2004).



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