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U.S. Department of Energy
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CaO interactions in the staged combustion of coal. Fifth quarterly technical progress report, October 1, 1981-December 31, 1981

Technical Report ·
OSTI ID:5751614
Study of the reaction of sulfur bearing compounds with CaO to form CaS was completed. A study of the oxidation of CaS is well underway and a study of kinetic and chemical parameters governing CaS and CaSO/sub 4/ formation in staged combustion, was continued. The reaction of COS with CaO exhibited a weak temperature dependence in the range studied, 1144 to 1373/sup 0/K. The reaction followed first order kinetics with respect to the unreacted calcium for both the COS-CaO and H/sub 2/S-CaO reactions. The addition of CO or H/sub 2/ to the COS or H/sub 2/S gas mixtures (to stabilize the COS or H/sub 2/S) had little or no influence on the reaction kinetics. The CaS oxidation studies indicate that the formation of CaSO/sub 4/ is slow at 1370/sup 0/K and that a significant amount of the original sulfur in the sample may have escaped, possibly as elemental sulfur or SO/sub 2/. At reaction times greater than 60 seconds, the major solid sulfur-bearing product was CaSO/sub 4/; below 60 seconds, large quantities of unreacted sulfide were evident. The results suggest that CaS oxidation to sulfate in the second stage of a two-stage combustion process may not proceed very rapidly. Results to date from the methane-coal studies show that sulfur retention in fuel-rich firings is dependent on reaction temperature and equivalence ratio. Approximately 85 percent sulfur retention is observed at postflame temperatures below 2000/sup 0/F and equivalence ratios of 1.7 to 1.9. At temperatures greater than 2000/sup 0/F, highest sulfur retention, approx. 75 percent, was observed at the lowest equivalence ratio used i.e. Phi = 1.3. These capture values were observed at short residence times, approx. 200 msec, and at a Ca/S mole ratio of 3.8.
Research Organization:
Battelle Columbus Labs., OH (USA)
DOE Contract Number:
AC22-80PC30301
OSTI ID:
5751614
Report Number(s):
DOE/PC/30301-5; ON: DE82010299
Country of Publication:
United States
Language:
English