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Removal of Hydrogen Sulfide and Ammonia by Goethite-Rich Limonite in the Coexistence of Coke Oven Gas Components

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/79332

Title: Removal of Hydrogen Sulfide and Ammonia by Goethite-Rich Limonite in the Coexistence of Coke Oven Gas Components
Authors: Mochizuki, Yuuki Browse this author →KAKEN DB
Ogawa, Ayumu Browse this author
Tsubouchi, Naoto Browse this author →KAKEN DB
Keywords: hydrogen sulfide
ammonia
removal
decomposition
catalyst
limonite
coke oven gas
Issue Date: 15-Mar-2017
Publisher: Iron and Steel Institute of Japan
Journal Title: ISIJ International
Volume: 57
Issue: 3
Start Page: 435
End Page: 442
Publisher DOI: 10.2355/isijinternational.ISIJINT-2016-561
Abstract: Hydrogen sulfide (H2S) removal and catalytic ammonia (NH3) decomposition performance of limonite in the presence of coke oven gas (COG) components has been studied in a cylindrical quartz reactor at 300–850°C under a high space velocity of 51000 h−1 to develop a novel hot gas cleanup method. The H2S removal behavior in 50% H2/He depends on the temperature, with high performance observed at lower temperature. An investigation of the removal behavior of H2S in the presence of COG components (CH4, CO, CO2 and H2O) at 400°C reveals that CH4 does not affect the removal performance. On the other hand, the coexistence of CO drastically decreases the H2S removal performance. However, the addition of 5% H2O to 50% H2/30% CH4/5% CO/He dramatically improves the H2S removal performance, whereas the performance is low at 5% CO2 with 50% H2/30% CH4/5% CO/He. In addition, the H2S breakthrough curve strongly depends on the space velocity. The limonite catalyst achieves almost complete decomposition of NH3 in He at 850°C until 240 min. When the decomposition run is performed in the presence of COG components, the coexistence of 30% CH4 deactivates limonite with significant formation of deposited carbon. On the other hand, the addition of 5% CO2, 5% H2O or 5% CO2/5% H2O to 50% H2/30% CH4/5% CO improves the catalytic activity without carbon deposition, and >99% conversion of NH3 to N2 is maintained until 240 min.
Rights: 著作権は日本鉄鋼協会にある
Type: article
URI: http://hdl.handle.net/2115/79332
Appears in Collections:工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 坪内 直人

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