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Fundamentals of nitric oxide formation in fossil fuel combustion. Quarterly progress report, 11 September--10 December 1976. [5 refs]

Technical Report ·
DOI:https://doi.org/10.2172/7099818· OSTI ID:7099818
A study of the reaction mechanism which leads to NO formation from fuel-nitrogen by determining the rates and mechanisms of pyridine pyrolysis and cyanogen oxidation was continued. The emphasis was shifted to the determination of the rate of formation of HCN since in previous studies it was found to be the major product containing the nitrogen during pyridine pyrolysis at higher temperatures (essentially 100% of the nitrogen appeared as HCN at 1100/sup 0/C). Because of the unreliability found in data from HCN chromatographic peak heights, the determinations are being done by wet chemical methods and these experiments are just underway. The oxidation of cyanogen has concentrated on a material balance. Using a one meter gas cell, infrared spectra of the products indicate that CO/sub 2/ is the only major oxidation product in the 950-1050/sup 0/C range. Small amounts of N/sub 2/O were found but no NO was observed; thus, it appears that most of the nitrogen from the reaction ends up in the elemental form. The significance of these observations to the overall project is that NO/sub x/ formation from fuel-nitrogen appears minor if fuel pyrolysis to CN type species takes place before oxidation. However, since fuel-nitrogen does contribute significantly to NO/sub x/ formation during coal combustion, the oxidizer must influence the products during the pyrolytic stage.
Research Organization:
Western Michigan Univ., Kalamazoo (USA). Dept. of Chemistry
OSTI ID:
7099818
Report Number(s):
FE-2018-6
Country of Publication:
United States
Language:
English