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Title Effect of Trace Combustion Species on SNCR Performance
Creator Teixeira, Donald P.; Muzio, Lawrence J.; Montgomery, Tami A.
Publisher Digitized by J. Willard Marriott Library, University of Utah
Date 1991
Spatial Coverage presented at Honolulu, Hawaii
Abstract The results of laboratory tests to evaluate the effect of trace combustion species on N2O production for the selective non-catalytic reduction NOx reduction process (SNCR) are presented. The tests were conducted under controlled conditions in a 200,000 Btu/hr laboratory pilot test combustion facility. Parameters investigated during the tests were: type of reducing agent (urea and ammonia); concentration of reducing agent relative to initial NOx concentration (N/NO - 0,1,2); temperature; carbon monoxide (CO) level (0-2000 ppm); and initial NOx level of 125 ppm. Results are presented which show the effect of these parameters on the NOx removal temperature "window", final CO emissions, "leak" NH3 emissions, and resulting N2O emissions. Several phenomenon not previously reported are described. Of particular interest is the effect of the initial CO level on N2O production for urea and ammonia. N2O levels are found to be significantly different for these two reagents. The implications of these results for practical combustion systems are discussed.
Type Text
Format application/pdf
Language eng
Rights This material may be protected by copyright. Permission required for use in any form. For further information please contact the American Flame Research Committee.
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Scanning Technician Cliodhna Davis
ARK ark:/87278/s6ns0xgs
Setname uu_afrc
ID 7067
Reference URL https://collections.lib.utah.edu/ark:/87278/s6ns0xgs

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Title Page 5
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OCR Text istaltic pumps and metered with rotameters. In order to maintain a constant thermal environment in the test section, the total amount of liquid injection was held constant at nominally 1 liter/hr. By diluting a concentrated rea­gent solution with distilled water, the amount of chemical reagent was varied while the total liquid flow rate was maintained. At a N/NO ratio of 2.0 the solution concentrations were 1.46 mole \ nitrogen (i.e., 2.4 wt\ for urea and 1.4 wt\ for ammonium hydroxide). For the cases where 00 was added to the process, this was done by injecting the CO along with the atomizing air. Gas samples were taken at the exit of the combustor with a water-cooled probe and transported to a series of gas analyzers (NO/NOx ' NH3' N20, CO, C02' and 02). The continuous measurement of N20 was made using an NDIR based tech­nique( 5). NH3 was measured using a Perkin-Elmer Mekos 100 continuous ana­lyzer. The Mekos 100 is an infrared analyzer; the entire sampling system including the sample cell of the analyzer is heat traced to 250oC. In the results which follow, removal of NO is presented rather than NOx (NO + N02). This was necessitated by the sampling train configuration utilized during the test series; however, previous tests have showed that for the range of parameters investigated, no N02 was produced (4). RESULTS Urea with Carbon Monoxide Previously, it has been observed that CO present in relatively small quanti­ties during the urea SNCR process results in the following behavior (4): o Widens the effective temperature "window". o Shifts the temperature "window" to a lower regime. o Lowers the peak removal efficiency. o Reduces unreacted ammonia byproducts. o Increases N20 emissions. This behavior can be readily seen in Figures 2 through 5 for the case of ini­tial NOx of 125 ppm, N/NO of 2, and CO levels ranging from 0 to 2000 ppm. As can be seen, N20 levels increase significantly as CO levels increase over the temperature range investigated. Peak N20 levels for the test conditions were about 25-30 ppm. The present data compare favorably with earlier data (4) collected on a different apparatus. In the earlier system, peak N20 levels of about 30-35 ppm were noted under similar conditions. Ammonia with Carbon Monoxide More recently, tests similar to those discussed above for urea have been con­ducted using aqueous ammonia a8 the selective reducing reagent. Results of these tests are shown in Figure 6 through 9. These figures present NO removal efficiency, CO characteristics, unreacted ammonia, and N20, respec­tively. Each of these results are discussed below. As in the case with 5
Setname uu_afrc
ID 7057
Reference URL https://collections.lib.utah.edu/ark:/87278/s6ns0xgs/7057