Biomass-Derived Butadiene by Dehydra-Decyclization of Tetrahydrofuran
Catalytic ring-opening dehydration of tetrahydrofuran (THF), itself a product of decarbonylation and reduction of biomass-derived furfural, yields 1,3-butadiene, an important monomer in rubbers and elastomers. It is demonstrated that dehydra-decyclization of THF with phosphorus-containing siliceous...
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Veröffentlicht in: | ACS sustainable chemistry & engineering 2017-05, Vol.5 (5), p.3732-3736 |
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creator | Abdelrahman, Omar A Park, Dae Sung Vinter, Katherine P Spanjers, Charles S Ren, Limin Cho, Hong Je Vlachos, Dionisios G Fan, Wei Tsapatsis, Michael Dauenhauer, Paul J |
description | Catalytic ring-opening dehydration of tetrahydrofuran (THF), itself a product of decarbonylation and reduction of biomass-derived furfural, yields 1,3-butadiene, an important monomer in rubbers and elastomers. It is demonstrated that dehydra-decyclization of THF with phosphorus-containing siliceous self-pillared pentasil (SPP) or MFI structure exhibits high selectivity to butadiene (85–99%) at both low (9%) and high (89%) conversion of THF. High selectivity to pentadiene and hexadiene was also obtained from 2-methyl-tetrahydrofuran and 2,5-dimethyl-tetrahydrofuran, respectively, with phosphorus-containing, all-silica zeolites. |
doi_str_mv | 10.1021/acssuschemeng.7b00745 |
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High selectivity to pentadiene and hexadiene was also obtained from 2-methyl-tetrahydrofuran and 2,5-dimethyl-tetrahydrofuran, respectively, with phosphorus-containing, all-silica zeolites.</description><identifier>ISSN: 2168-0485</identifier><identifier>EISSN: 2168-0485</identifier><identifier>DOI: 10.1021/acssuschemeng.7b00745</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>catalysis (homogeneous), catalysis (heterogeneous), biofuels (including algae and biomass), bio-inspired, hydrogen and fuel cells, materials and chemistry by design, synthesis (novel materials), synthesis (self-assembly), synthesis (scalable processing)</subject><ispartof>ACS sustainable chemistry & engineering, 2017-05, Vol.5 (5), p.3732-3736</ispartof><rights>Copyright © 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a322t-1ae8754aa409bfb94d9c1ba07736a96ff83c19b9cf2bc98d1652d2077d29a5053</citedby><cites>FETCH-LOGICAL-a322t-1ae8754aa409bfb94d9c1ba07736a96ff83c19b9cf2bc98d1652d2077d29a5053</cites><orcidid>0000-0001-5810-1953 ; 0000000158101953</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acssuschemeng.7b00745$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acssuschemeng.7b00745$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1388987$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Abdelrahman, Omar A</creatorcontrib><creatorcontrib>Park, Dae Sung</creatorcontrib><creatorcontrib>Vinter, Katherine P</creatorcontrib><creatorcontrib>Spanjers, Charles S</creatorcontrib><creatorcontrib>Ren, Limin</creatorcontrib><creatorcontrib>Cho, Hong Je</creatorcontrib><creatorcontrib>Vlachos, Dionisios G</creatorcontrib><creatorcontrib>Fan, Wei</creatorcontrib><creatorcontrib>Tsapatsis, Michael</creatorcontrib><creatorcontrib>Dauenhauer, Paul J</creatorcontrib><creatorcontrib>Energy Frontier Research Centers (EFRC) (United States). 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Catalysis Center for Energy Innovation (CCEI)</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>ACS sustainable chemistry & engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abdelrahman, Omar A</au><au>Park, Dae Sung</au><au>Vinter, Katherine P</au><au>Spanjers, Charles S</au><au>Ren, Limin</au><au>Cho, Hong Je</au><au>Vlachos, Dionisios G</au><au>Fan, Wei</au><au>Tsapatsis, Michael</au><au>Dauenhauer, Paul J</au><aucorp>Energy Frontier Research Centers (EFRC) (United States). Catalysis Center for Energy Innovation (CCEI)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biomass-Derived Butadiene by Dehydra-Decyclization of Tetrahydrofuran</atitle><jtitle>ACS sustainable chemistry & engineering</jtitle><addtitle>ACS Sustainable Chem. Eng</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>5</volume><issue>5</issue><spage>3732</spage><epage>3736</epage><pages>3732-3736</pages><issn>2168-0485</issn><eissn>2168-0485</eissn><abstract>Catalytic ring-opening dehydration of tetrahydrofuran (THF), itself a product of decarbonylation and reduction of biomass-derived furfural, yields 1,3-butadiene, an important monomer in rubbers and elastomers. It is demonstrated that dehydra-decyclization of THF with phosphorus-containing siliceous self-pillared pentasil (SPP) or MFI structure exhibits high selectivity to butadiene (85–99%) at both low (9%) and high (89%) conversion of THF. 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title | Biomass-Derived Butadiene by Dehydra-Decyclization of Tetrahydrofuran |
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