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High temperature gas desulfurization with elemental sulfur production
Preliminary results on the use of cerium oxide as a high-temperature desulfurization sorbent are presented. The primary advantage of cerium over current zinc-based sorbents is the potential to produce elemental sulfur during the regeneration phase of the process. Although CeO 2 is less effective for...
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Published in: | Chemical engineering science 1999, Vol.54 (15), p.3007-3017 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Preliminary results on the use of cerium oxide as a high-temperature desulfurization sorbent are presented. The primary advantage of cerium over current zinc-based sorbents is the potential to produce elemental sulfur during the regeneration phase of the process. Although CeO
2 is less effective for H
2S removal during sulfidation, the sulfided product, Ce
2O
2S, will react with SO
2 to produce elemental sulfur directly. Rapid and complete regeneration is possible over the range of 500 to 700°C, and only elemental sulfur is formed. Elemental sulfur concentrations (considered as S
2) as large as 20
mol% have been produced in the regeneration product. The sorbent has been subjected to ten sulfidation–regeneration cycles using a laboratory-scale fixed-bed reactor with negligible activity loss. Effectively complete conversion of CeO
2 to Ce
2O
2S during sulfidation and subsequent regeneration to CeO
2 was achieved in each cycle. A two-stage desulfurization process using CeO
2 for bulk H
2S removal followed by a zinc sorbent polishing step has been proposed to meet specifications of the integrated gasification combined cycle (IGCC) process. Economic comparison with a single-stage desulfurization process using zinc sorbent followed by elemental sulfur recovery using the direct sulfur recovery process (DSRP) shows that the two-stage cerium process may be less costly if the cerium sorbent is sufficiently durable. |
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ISSN: | 0009-2509 1873-4405 |
DOI: | 10.1016/S0009-2509(98)00427-8 |