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Title: Kinetics of Mn-based sorbents for hot coal gas desulfurization. Quarterly progress report, September 15, 1995--December 15, 1995

Technical Report ·
DOI:https://doi.org/10.2172/206994· OSTI ID:206994

The Morgantown Energy Technology Center (METC) of the U.S. Department of Energy (DOE) is actively pursuing the development of reliable and cost-effective processes to clean coal gasifier gases for application to integrated gasification combined cycle (IGCC) and molten carbonate fuel cell (MCFC) power plants. A large portion of gas cleanup research has been directed towards hot gas desulfurization using Zn-based sorbents. However, zinc titanate sorbents undergo reduction to the metal at temperatures approaching 700{degrees}C and lose reactivity because of volatilization. In addition, sulfate formation during regeneration leads to spalling of reactive surfaces. Because of these problems with zinc-based sorbents, METC has shown interest in formulating and testing manganese-based sorbents. Currently, many proposed IGCC processes include a water quench prior to desulfurization. This quench is required for two reasons; limitations in the process hardware (1000{degrees}C), and excessive Zn-based sorbent loss (about 700{degrees}C). With manganese, the water quench is not necessary to avoid sorbent loss, since Mn-based sorbents have been shown to retain reactivity under cyclic testing at 900{degrees}C. This advantage of manganese over zinc has potential to increase thermal efficiency as the trade-off of increasing the equilibrium H{sub 2}S over-pressure obtainable with a manganese sorbent. In the work which is reported here, lower loading temperatures (as low as 400{degrees}C) are studied. Also formulations containing titania rather then alumina are studied to attempt to improve performance.

Research Organization:
Minnesota Univ., Minneapolis, MN (United States). Dept. of Civil and Mineral Engineering
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
FG22-94PC94212
OSTI ID:
206994
Report Number(s):
DOE/PC/94212-T5; ON: DE96007564; TRN: 96:002297
Resource Relation:
Other Information: PBD: 15 Dec 1995
Country of Publication:
United States
Language:
English