IMR OpenIR
Direct Conversion of Acetylene and 1,2-Dichloroethane to Vinyl Chloride Monomer over a Supported Carbon Nitride Catalyst: Tunable Activity Controlled by the Synthesis Temperature
Sun, Xi1; Liu, Xi4; Qin, Yucai2; Qiang, Li2; He, Yu-Peng2; Su, Dangsheng3; Song, Lijuan2; Sun, Zhaolin1
Corresponding AuthorSu, Dangsheng(dssu@dicp.ac.cn) ; Song, Lijuan(lsong56@263.net) ; Sun, Zhaolin(zlsun56@263.net)
2019-04-10
Source PublicationINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
ISSN0888-5885
Volume58Issue:14Pages:5404-5413
AbstractA carbon supported carbon nitride is reported here as a catalyst for the direct conversion of acetylene and 1,2-dichloroethane (EDC) to vinyl chloride monomer (VCM). We demonstrate that increasing the synthesis temperature of the carbon nitride material leads to a catalyst with higher catalytic activity toward VCM production. The catalysts were characterized by acetylene temperature-programmed desorption, X-ray photoelectron spectroscopy, high-resolution TEM, electron energy loss spectroscopy, and computational methods, showing that the improved activity for the catalysts can be ascribed to both the higher proportion of pyridinic N and the more positive lowest unoccupied molecular orbital of the catalyst, resulting from the increased degree of polymerization of carbon nitride. These findings highlight the role of polymerization conditions in increasing the catalytic activity of carbon nitride catalysts and provide a strategy for the selective synthesis of highly active carbon nitride catalysts for the one-step synthesis of VCM from acetylene and EDC.
Funding OrganizationNational Science Foundation of China ; Department of Science and Technology of Liaoning Province
DOI10.1021/acs.iecr.8b05942
Indexed BySCI
Language英语
Funding ProjectNational Science Foundation of China[21376114] ; National Science Foundation of China[U1662135] ; National Science Foundation of China[21673273] ; Department of Science and Technology of Liaoning Province[2013219006]
WOS Research AreaEngineering
WOS SubjectEngineering, Chemical
WOS IDWOS:000464769200006
PublisherAMER CHEMICAL SOC
Citation statistics
Cited Times:3[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.imr.ac.cn/handle/321006/132919
Collection中国科学院金属研究所
Corresponding AuthorSu, Dangsheng; Song, Lijuan; Sun, Zhaolin
Affiliation1.Lanzhou Univ, Dept Chem, 222 South Tianshui Rd, Lanzhou 730000, Gansu, Peoples R China
2.Liaoning Shihua Univ, Key Lab Petrochem Catalyt Sci & Technol Liaoning, Fushun 113001, Liaoning, Peoples R China
3.Chinese Acad Sci, Inst Met Res, Shenyang 110016, Liaoning, Peoples R China
4.Synfuels China Technol Co Ltd, Syncat Beijing, Beijing 101407, Peoples R China
Recommended Citation
GB/T 7714
Sun, Xi,Liu, Xi,Qin, Yucai,et al. Direct Conversion of Acetylene and 1,2-Dichloroethane to Vinyl Chloride Monomer over a Supported Carbon Nitride Catalyst: Tunable Activity Controlled by the Synthesis Temperature[J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,2019,58(14):5404-5413.
APA Sun, Xi.,Liu, Xi.,Qin, Yucai.,Qiang, Li.,He, Yu-Peng.,...&Sun, Zhaolin.(2019).Direct Conversion of Acetylene and 1,2-Dichloroethane to Vinyl Chloride Monomer over a Supported Carbon Nitride Catalyst: Tunable Activity Controlled by the Synthesis Temperature.INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,58(14),5404-5413.
MLA Sun, Xi,et al."Direct Conversion of Acetylene and 1,2-Dichloroethane to Vinyl Chloride Monomer over a Supported Carbon Nitride Catalyst: Tunable Activity Controlled by the Synthesis Temperature".INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH 58.14(2019):5404-5413.
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Sun, Xi]'s Articles
[Liu, Xi]'s Articles
[Qin, Yucai]'s Articles
Baidu academic
Similar articles in Baidu academic
[Sun, Xi]'s Articles
[Liu, Xi]'s Articles
[Qin, Yucai]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Sun, Xi]'s Articles
[Liu, Xi]'s Articles
[Qin, Yucai]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.