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Development of combined nitrogen oxide/sulfur oxide environmental-control technology

Technical Report ·
OSTI ID:5257521
Using a statistically designed series of batch experiments, we investigated simultaneous desulfurization and denitrification of flue gas from coal-fired boilers. Our results were consistent with mechanisms in which NO (nitrogen monoxide) and NO/sub 2/ (nitrogen dioxide) are coscrubbed as HNO/sub 2/ (nitrous acid), which reacts with SO/sub 2/ (sulfur dioxide) as (HSO/sub 3//sup -/) (the bisulfite ion) to form hydroxylamine-N-sulfonates. Significant pathways for aqueous-phase denitrification were available at pH values between 4 and 9, with an optimum at a pH value of 6.9. This report shows how these mechanisms operated in a variety of scrubber technologies, so that successful control strategies can be developed. Four desulfurization chemistries were ranked in terms of their denitrification potential, in the following order: double-alkali > lime > citrate > Dowa. A synthetic flue gas containing nitrogen blended with carbon dioxide (14.5%), oxygen (5.1%), SO/sub 2/ (1500 or 3000 ppM), NO (475 or 450 ppM), NO/sub 2/ (25 or 50 ppM), and water vapor (8%) was fed at 100 L/min (standard) to a 3.6-L batch sparger. Additives investigated included FeSO/sub 4/ (ferrous sulfate), Fe(II)EDTA, Cu(II)EDTA, Fe(II)NTA, Fe(OH)/sub 2/ (ferrous hydroxide), NH/sub 4/OH (ammonium hydroxide), and N/sub 2/H/sub 4/ (hydrazine), where EDTA signifies ethylenediaminetetraacetic acid and NTA signifies nitrilotriacetic acid. Of these additives, Fe(II)EDTA performed best as an enhancer of NO/sub x/ (nitrogen oxides) removal.
Research Organization:
Argonne National Lab., IL (USA)
DOE Contract Number:
W-31109-ENG-38
OSTI ID:
5257521
Report Number(s):
ANL/ECT-14; ON: DE86001301
Country of Publication:
United States
Language:
English