Plasma enhanced C1-chemistry: towards greener methane conversion
Direct conversion of methane to methanol is considered as a promising next-generation green technology, because it would eliminate energy intense, high temperature syngas production. Before 2000, various catalysts and thermochemical reaction systems were investigated towards converting direct methan...
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De Gruyter
2012-12-01
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Online Access: | https://doi.org/10.1515/gps-2012-0074 |
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doaj-a0df8d987aa1434cb3ac38fca7e065612021-10-02T17:47:21ZengDe GruyterGreen Processing and Synthesis2191-95422191-95502012-12-011651752310.1515/gps-2012-0074Plasma enhanced C1-chemistry: towards greener methane conversionNozaki Tomohiro0Okazaki Ken1Department of Mechanical Sciences and Engineering, Tokyo Institute of Technology, 2–12–1, Ookayama, Meguro, Tokyo 1528550, JapanDepartment of Mechanical and Control Engineering, Tokyo Institute of Technology, 2–12–1, Ookayama, Meguro, Tokyo 1528550, JapanDirect conversion of methane to methanol is considered as a promising next-generation green technology, because it would eliminate energy intense, high temperature syngas production. Before 2000, various catalysts and thermochemical reaction systems were investigated towards converting direct methane to methanol; however, one-pass yield of methanol was <5%. More recently, bioreaction and photochemical synthesis have attracted keen attention, because these processes use renewable solar energy. However, the yield and productivity are still the main issues. This paper presents a low temperature (<600 K), direct conversion of methane to methanol/syngas via non-thermal plasma technology, which enables one-pass liquid yield of 20% (sum of CH3OH, HCHO and HCOOH), with selectivity between 40 and 60%. First, it emphasizes the impact of plasma catalysis in the future sustainable energy system. Second, the principle of micro-channel plasma chemical reactor is presented, then experimental results are overviewed based on our work. Finally, concluding remarks are provided.https://doi.org/10.1515/gps-2012-0074c1-chemistrymicrochemical reactornonthermal plasmaplasma catalysisprocess intensification |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nozaki Tomohiro Okazaki Ken |
spellingShingle |
Nozaki Tomohiro Okazaki Ken Plasma enhanced C1-chemistry: towards greener methane conversion Green Processing and Synthesis c1-chemistry microchemical reactor nonthermal plasma plasma catalysis process intensification |
author_facet |
Nozaki Tomohiro Okazaki Ken |
author_sort |
Nozaki Tomohiro |
title |
Plasma enhanced C1-chemistry: towards greener methane conversion |
title_short |
Plasma enhanced C1-chemistry: towards greener methane conversion |
title_full |
Plasma enhanced C1-chemistry: towards greener methane conversion |
title_fullStr |
Plasma enhanced C1-chemistry: towards greener methane conversion |
title_full_unstemmed |
Plasma enhanced C1-chemistry: towards greener methane conversion |
title_sort |
plasma enhanced c1-chemistry: towards greener methane conversion |
publisher |
De Gruyter |
series |
Green Processing and Synthesis |
issn |
2191-9542 2191-9550 |
publishDate |
2012-12-01 |
description |
Direct conversion of methane to methanol is considered as a promising next-generation green technology, because it would eliminate energy intense, high temperature syngas production. Before 2000, various catalysts and thermochemical reaction systems were investigated towards converting direct methane to methanol; however, one-pass yield of methanol was <5%. More recently, bioreaction and photochemical synthesis have attracted keen attention, because these processes use renewable solar energy. However, the yield and productivity are still the main issues. This paper presents a low temperature (<600 K), direct conversion of methane to methanol/syngas via non-thermal plasma technology, which enables one-pass liquid yield of 20% (sum of CH3OH, HCHO and HCOOH), with selectivity between 40 and 60%. First, it emphasizes the impact of plasma catalysis in the future sustainable energy system. Second, the principle of micro-channel plasma chemical reactor is presented, then experimental results are overviewed based on our work. Finally, concluding remarks are provided. |
topic |
c1-chemistry microchemical reactor nonthermal plasma plasma catalysis process intensification |
url |
https://doi.org/10.1515/gps-2012-0074 |
work_keys_str_mv |
AT nozakitomohiro plasmaenhancedc1chemistrytowardsgreenermethaneconversion AT okazakiken plasmaenhancedc1chemistrytowardsgreenermethaneconversion |
_version_ |
1716850563967090688 |