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Microalgae lipids as a feedstock for the production of benzene

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PINGEN, Dennis, Julia ZIMMERER, Nele KLINKENBERG, Stefan MECKING, 2018. Microalgae lipids as a feedstock for the production of benzene. In: Green Chemistry. 20(8), pp. 1874-1878. ISSN 1463-9262. eISSN 1463-9270. Available under: doi: 10.1039/c8gc00423d

@article{Pingen2018Micro-42418, title={Microalgae lipids as a feedstock for the production of benzene}, year={2018}, doi={10.1039/c8gc00423d}, number={8}, volume={20}, issn={1463-9262}, journal={Green Chemistry}, pages={1874--1878}, author={Pingen, Dennis and Zimmerer, Julia and Klinkenberg, Nele and Mecking, Stefan} }

<rdf:RDF xmlns:dcterms="" xmlns:dc="" xmlns:rdf="" xmlns:bibo="" xmlns:dspace="" xmlns:foaf="" xmlns:void="" xmlns:xsd="" > <rdf:Description rdf:about=""> <dc:contributor>Klinkenberg, Nele</dc:contributor> <bibo:uri rdf:resource=""/> <dc:creator>Pingen, Dennis</dc:creator> <dc:contributor>Zimmerer, Julia</dc:contributor> <dc:date rdf:datatype="">2018-05-23T09:08:53Z</dc:date> <dc:contributor>Pingen, Dennis</dc:contributor> <dcterms:title>Microalgae lipids as a feedstock for the production of benzene</dcterms:title> <dcterms:isPartOf rdf:resource=""/> <dc:creator>Klinkenberg, Nele</dc:creator> <dspace:hasBitstream rdf:resource=""/> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dcterms:rights rdf:resource=""/> <dc:language>eng</dc:language> <dc:creator>Mecking, Stefan</dc:creator> <dc:rights>terms-of-use</dc:rights> <dc:creator>Zimmerer, Julia</dc:creator> <dcterms:issued>2018</dcterms:issued> <dspace:isPartOfCollection rdf:resource=""/> <dcterms:hasPart rdf:resource=""/> <dcterms:available rdf:datatype="">2018-05-23T09:08:53Z</dcterms:available> <foaf:homepage rdf:resource="http://localhost:8080/jspui"/> <dc:contributor>Mecking, Stefan</dc:contributor> <dcterms:abstract xml:lang="eng">A two-step one-pot synthesis of benzene from the five-fold unsaturated fatty acid eicosapentaenoic acid (EPA), a component of microalgae oils, is presented. By a sequence of olefin metathesis and the catalytic dehydrogenation of the resulting 1,4-cyclohexadiene, two equivalents of benzene are effectively formed per EPA substrate molecule. As the only major by-products, 5-octenoic acid and 5-decenedioic acid are formed. Performing the dehydrogenation step under hydrogen pressure results in the formation of their saturated analogues, sebacic acid and octanoic acid, both desirable products, while the simultaneous dehydrogenation step to benzene is not hampered.</dcterms:abstract> <dspace:isPartOfCollection rdf:resource=""/> <dcterms:isPartOf rdf:resource=""/> </rdf:Description> </rdf:RDF>

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