Partial oxidation of methane by photocatalysis
Methane chemistry is one of the “Holy Grails of catalysis”. It is highly desirable but challenge to transform methane into value-added chemicals, because of its high C-H bonding energy (435 kJ mol−1), lack of π bonding or unpaired electrons. Currently, commercial methane conversion is usually carrie...
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Veröffentlicht in: | Chinese chemical letters 2024-01, Vol.35 (1), p.108418-168, Article 108418 |
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creator | Yang, Zhongshan Zhang, Qiqi Song, Hui Chen, Xin Cui, Jiwei Sun, Yanhui Liu, Lequan Ye, Jinhua |
description | Methane chemistry is one of the “Holy Grails of catalysis”. It is highly desirable but challenge to transform methane into value-added chemicals, because of its high C-H bonding energy (435 kJ mol−1), lack of π bonding or unpaired electrons. Currently, commercial methane conversion is usually carried out in harsh conditions with enormous energy input. Photocatalytic partial oxidation of methane to liquid oxygenates (PPOMO) is a future-oriented technology towards realizing high efficiency and high selectivity under mild conditions. The selection of oxidant is crucial to the PPOMO performance. Hence, attentions are paid to the research progress of PPOMO with various oxidants (O2, H2O, H2O2 and other oxidants). Moreover, the activation of the selected oxidants is also highly emphasized. Meanwhile, we summarized the methane activation mechanisms focusing on the C-H bond that was broken mainly by •OH radical, O− specie or photogenerated hole (h+). Finally, the challenges and prospects in this subject are briefly discussed.
[Display omitted]
Progress in partial oxidation of methane to liquid oxygenates with various oxidants (H2O, H2O2 or O2) by photocatalysis is systematically summarized. The activation of selected oxidant is highlighted. Methane activated mainly by •OH radicals, O− species or photogenerated hole (h+) is also highly emphasized. |
doi_str_mv | 10.1016/j.cclet.2023.108418 |
format | Article |
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[Display omitted]
Progress in partial oxidation of methane to liquid oxygenates with various oxidants (H2O, H2O2 or O2) by photocatalysis is systematically summarized. The activation of selected oxidant is highlighted. Methane activated mainly by •OH radicals, O− species or photogenerated hole (h+) is also highly emphasized.</description><identifier>ISSN: 1001-8417</identifier><identifier>EISSN: 1878-5964</identifier><identifier>DOI: 10.1016/j.cclet.2023.108418</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>C-H activation ; Liquid oxygenates ; Oxidants ; Partial oxidation of methane ; Photocatalysis</subject><ispartof>Chinese chemical letters, 2024-01, Vol.35 (1), p.108418-168, Article 108418</ispartof><rights>2023</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c335t-8184147ab119debe9c062a1c2ba6cbf8a9775b211d2015a0ef30d6dda56119d13</citedby><cites>FETCH-LOGICAL-c335t-8184147ab119debe9c062a1c2ba6cbf8a9775b211d2015a0ef30d6dda56119d13</cites><orcidid>0000-0002-3989-3905</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/zghxkb/zghxkb.jpg</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids></links><search><creatorcontrib>Yang, Zhongshan</creatorcontrib><creatorcontrib>Zhang, Qiqi</creatorcontrib><creatorcontrib>Song, Hui</creatorcontrib><creatorcontrib>Chen, Xin</creatorcontrib><creatorcontrib>Cui, Jiwei</creatorcontrib><creatorcontrib>Sun, Yanhui</creatorcontrib><creatorcontrib>Liu, Lequan</creatorcontrib><creatorcontrib>Ye, Jinhua</creatorcontrib><title>Partial oxidation of methane by photocatalysis</title><title>Chinese chemical letters</title><description>Methane chemistry is one of the “Holy Grails of catalysis”. It is highly desirable but challenge to transform methane into value-added chemicals, because of its high C-H bonding energy (435 kJ mol−1), lack of π bonding or unpaired electrons. Currently, commercial methane conversion is usually carried out in harsh conditions with enormous energy input. Photocatalytic partial oxidation of methane to liquid oxygenates (PPOMO) is a future-oriented technology towards realizing high efficiency and high selectivity under mild conditions. The selection of oxidant is crucial to the PPOMO performance. Hence, attentions are paid to the research progress of PPOMO with various oxidants (O2, H2O, H2O2 and other oxidants). Moreover, the activation of the selected oxidants is also highly emphasized. Meanwhile, we summarized the methane activation mechanisms focusing on the C-H bond that was broken mainly by •OH radical, O− specie or photogenerated hole (h+). Finally, the challenges and prospects in this subject are briefly discussed.
[Display omitted]
Progress in partial oxidation of methane to liquid oxygenates with various oxidants (H2O, H2O2 or O2) by photocatalysis is systematically summarized. The activation of selected oxidant is highlighted. Methane activated mainly by •OH radicals, O− species or photogenerated hole (h+) is also highly emphasized.</description><subject>C-H activation</subject><subject>Liquid oxygenates</subject><subject>Oxidants</subject><subject>Partial oxidation of methane</subject><subject>Photocatalysis</subject><issn>1001-8417</issn><issn>1878-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPxDAQhC0EEsfBL6BJR5XgzdMpKNCJl3QSFFBbG9u5c8jFJ9vAhV-PQ6ipdjWab1czhFwCTYBCed0lQvTKJylNs6CwHNgRWQCrWFzUZX4cdkohDnp1Ss6c6yhNGcvKBUle0HqNfWQOWqLXZohMG-2U3-KgomaM9lvjjUCP_ei0OycnLfZOXfzNJXm7v3tdPcbr54en1e06FllW-JhBeJVX2ADUUjWqFrRMEUTaYCmalmFdVUWTAsiUQoFUtRmVpZRYlBMB2ZJczXe_cGhx2PDOfNghfOTfm-3hvQlBczpFD85sdgprnLOq5Xurd2hHDpRPDt7x33L4VA6fywnUzUypEOJTK8ud0GoQSmqrhOfS6H_5H-kUbW8</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Yang, Zhongshan</creator><creator>Zhang, Qiqi</creator><creator>Song, Hui</creator><creator>Chen, Xin</creator><creator>Cui, Jiwei</creator><creator>Sun, Yanhui</creator><creator>Liu, Lequan</creator><creator>Ye, Jinhua</creator><general>Elsevier B.V</general><general>Zhejiang LAMP Co.,Ltd.,Wenzhou 325206,China%TJU-NIMS International Collaboration Laboratory,School of Materials Science and Engineering,Tianjin University,Tianjin 300072,China%International Center for Materials Nanoarchitectonics(WPI-MANA),National Institute for Materials Science(NIMS),1-1 Namiki,Ibaraki 3050047,Japan%TJU-NIMS International Collaboration Laboratory,School of Materials Science and Engineering,Tianjin University,Tianjin 300072,China</general><general>International Center for Materials Nanoarchitectonics(WPI-MANA),National Institute for Materials Science(NIMS),1-1 Namiki,Ibaraki 3050047,Japan</general><general>TJU-NIMS International Collaboration Laboratory,School of Materials Science and Engineering,Tianjin University,Tianjin 300072,China</general><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope><orcidid>https://orcid.org/0000-0002-3989-3905</orcidid></search><sort><creationdate>202401</creationdate><title>Partial oxidation of methane by photocatalysis</title><author>Yang, Zhongshan ; Zhang, Qiqi ; Song, Hui ; Chen, Xin ; Cui, Jiwei ; Sun, Yanhui ; Liu, Lequan ; Ye, Jinhua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-8184147ab119debe9c062a1c2ba6cbf8a9775b211d2015a0ef30d6dda56119d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>C-H activation</topic><topic>Liquid oxygenates</topic><topic>Oxidants</topic><topic>Partial oxidation of methane</topic><topic>Photocatalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Zhongshan</creatorcontrib><creatorcontrib>Zhang, Qiqi</creatorcontrib><creatorcontrib>Song, Hui</creatorcontrib><creatorcontrib>Chen, Xin</creatorcontrib><creatorcontrib>Cui, Jiwei</creatorcontrib><creatorcontrib>Sun, Yanhui</creatorcontrib><creatorcontrib>Liu, Lequan</creatorcontrib><creatorcontrib>Ye, Jinhua</creatorcontrib><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese chemical letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Zhongshan</au><au>Zhang, Qiqi</au><au>Song, Hui</au><au>Chen, Xin</au><au>Cui, Jiwei</au><au>Sun, Yanhui</au><au>Liu, Lequan</au><au>Ye, Jinhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Partial oxidation of methane by photocatalysis</atitle><jtitle>Chinese chemical letters</jtitle><date>2024-01</date><risdate>2024</risdate><volume>35</volume><issue>1</issue><spage>108418</spage><epage>168</epage><pages>108418-168</pages><artnum>108418</artnum><issn>1001-8417</issn><eissn>1878-5964</eissn><abstract>Methane chemistry is one of the “Holy Grails of catalysis”. It is highly desirable but challenge to transform methane into value-added chemicals, because of its high C-H bonding energy (435 kJ mol−1), lack of π bonding or unpaired electrons. Currently, commercial methane conversion is usually carried out in harsh conditions with enormous energy input. Photocatalytic partial oxidation of methane to liquid oxygenates (PPOMO) is a future-oriented technology towards realizing high efficiency and high selectivity under mild conditions. The selection of oxidant is crucial to the PPOMO performance. Hence, attentions are paid to the research progress of PPOMO with various oxidants (O2, H2O, H2O2 and other oxidants). Moreover, the activation of the selected oxidants is also highly emphasized. Meanwhile, we summarized the methane activation mechanisms focusing on the C-H bond that was broken mainly by •OH radical, O− specie or photogenerated hole (h+). Finally, the challenges and prospects in this subject are briefly discussed.
[Display omitted]
Progress in partial oxidation of methane to liquid oxygenates with various oxidants (H2O, H2O2 or O2) by photocatalysis is systematically summarized. The activation of selected oxidant is highlighted. Methane activated mainly by •OH radicals, O− species or photogenerated hole (h+) is also highly emphasized.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cclet.2023.108418</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-3989-3905</orcidid></addata></record> |
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subjects | C-H activation Liquid oxygenates Oxidants Partial oxidation of methane Photocatalysis |
title | Partial oxidation of methane by photocatalysis |
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