Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics

Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics

Ferulic acid and p-coumaric acid are abundant, biorenewable precursors for the synthesis of polyethylene ferulate (PEF) and polyethylene coumarate (PEC), as well as cognate copolymers with prescribed hydrogenation of the main-chain double bond. By controlling the comonomer feed ratios, copolymers wi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2015-01, Vol.17 (9), p.4512-4517
Hauptverfasser: Nguyen, Ha Thi Hoang, Reis, Marcus H, Qi, Pengxu, Miller, Stephen A
Format: Artikel
Sprache:eng
Schlagworte:
Bonding
Congeners
Copolymers
Hydrogenation
Polyethylenes
Polystyrene resins
Precursors
Thermal properties
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 4517
container_issue 9
container_start_page 4512
container_title Green chemistry : an international journal and green chemistry resource : GC
container_volume 17
creator Nguyen, Ha Thi Hoang
Reis, Marcus H
Qi, Pengxu
Miller, Stephen A
description Ferulic acid and p-coumaric acid are abundant, biorenewable precursors for the synthesis of polyethylene ferulate (PEF) and polyethylene coumarate (PEC), as well as cognate copolymers with prescribed hydrogenation of the main-chain double bond. By controlling the comonomer feed ratios, copolymers with tunable thermal properties are obtained, including the thermal range occupied by polystyrene (PS).
doi_str_mv 10.1039/c5gc01104c
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1744710419</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1712774010</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-881ec4e45f9762d1683eb6d78e02aee24bcbbdb968af858a7de294dad3b207bb3</originalsourceid><addsrcrecordid>eNqNkD1PwzAURS0EEqWw8As8FqSA7Ti2w4aitiBVogPMkT9eSpCTFDulyr8npYiZ6V29e3SHg9A1JXeUpPm9zTaWUEq4PUETykWa5EyS078s2Dm6iPGDjJAUfIL0uvMD9O-DhxZwBWHndQ94tp4vbrBuHbZduxmrEB_wdkRjP4QD2dRNbSN2EOovcLgKXYNN3R26vTYesB4_uh-ZS3RWaR_h6vdO0dti_lo8JauX5XPxuEosJ6RPlKJgOfCsyqVgjgqVghFOKiBMAzBurDHO5ELpSmVKSwcs50671DAijUmnaHbc3YbucwexL5s6WvBet9DtYkkl53I0Q_N_oJRJycmodIpuj6gNXYwBqnIb6kaHoaSkPCgvi2xZ_Cgv0m9xAXUp</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1712774010</pqid></control><display><type>article</type><title>Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Nguyen, Ha Thi Hoang ; Reis, Marcus H ; Qi, Pengxu ; Miller, Stephen A</creator><creatorcontrib>Nguyen, Ha Thi Hoang ; Reis, Marcus H ; Qi, Pengxu ; Miller, Stephen A</creatorcontrib><description>Ferulic acid and p-coumaric acid are abundant, biorenewable precursors for the synthesis of polyethylene ferulate (PEF) and polyethylene coumarate (PEC), as well as cognate copolymers with prescribed hydrogenation of the main-chain double bond. By controlling the comonomer feed ratios, copolymers with tunable thermal properties are obtained, including the thermal range occupied by polystyrene (PS).</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c5gc01104c</identifier><language>eng</language><subject>Bonding ; Congeners ; Copolymers ; Hydrogenation ; Polyethylenes ; Polystyrene resins ; Precursors ; Thermal properties</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2015-01, Vol.17 (9), p.4512-4517</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-881ec4e45f9762d1683eb6d78e02aee24bcbbdb968af858a7de294dad3b207bb3</citedby><cites>FETCH-LOGICAL-c400t-881ec4e45f9762d1683eb6d78e02aee24bcbbdb968af858a7de294dad3b207bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Nguyen, Ha Thi Hoang</creatorcontrib><creatorcontrib>Reis, Marcus H</creatorcontrib><creatorcontrib>Qi, Pengxu</creatorcontrib><creatorcontrib>Miller, Stephen A</creatorcontrib><title>Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>Ferulic acid and p-coumaric acid are abundant, biorenewable precursors for the synthesis of polyethylene ferulate (PEF) and polyethylene coumarate (PEC), as well as cognate copolymers with prescribed hydrogenation of the main-chain double bond. By controlling the comonomer feed ratios, copolymers with tunable thermal properties are obtained, including the thermal range occupied by polystyrene (PS).</description><subject>Bonding</subject><subject>Congeners</subject><subject>Copolymers</subject><subject>Hydrogenation</subject><subject>Polyethylenes</subject><subject>Polystyrene resins</subject><subject>Precursors</subject><subject>Thermal properties</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkD1PwzAURS0EEqWw8As8FqSA7Ti2w4aitiBVogPMkT9eSpCTFDulyr8npYiZ6V29e3SHg9A1JXeUpPm9zTaWUEq4PUETykWa5EyS078s2Dm6iPGDjJAUfIL0uvMD9O-DhxZwBWHndQ94tp4vbrBuHbZduxmrEB_wdkRjP4QD2dRNbSN2EOovcLgKXYNN3R26vTYesB4_uh-ZS3RWaR_h6vdO0dti_lo8JauX5XPxuEosJ6RPlKJgOfCsyqVgjgqVghFOKiBMAzBurDHO5ELpSmVKSwcs50671DAijUmnaHbc3YbucwexL5s6WvBet9DtYkkl53I0Q_N_oJRJycmodIpuj6gNXYwBqnIb6kaHoaSkPCgvi2xZ_Cgv0m9xAXUp</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Nguyen, Ha Thi Hoang</creator><creator>Reis, Marcus H</creator><creator>Qi, Pengxu</creator><creator>Miller, Stephen A</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U6</scope><scope>C1K</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20150101</creationdate><title>Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics</title><author>Nguyen, Ha Thi Hoang ; Reis, Marcus H ; Qi, Pengxu ; Miller, Stephen A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-881ec4e45f9762d1683eb6d78e02aee24bcbbdb968af858a7de294dad3b207bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Bonding</topic><topic>Congeners</topic><topic>Copolymers</topic><topic>Hydrogenation</topic><topic>Polyethylenes</topic><topic>Polystyrene resins</topic><topic>Precursors</topic><topic>Thermal properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Ha Thi Hoang</creatorcontrib><creatorcontrib>Reis, Marcus H</creatorcontrib><creatorcontrib>Qi, Pengxu</creatorcontrib><creatorcontrib>Miller, Stephen A</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nguyen, Ha Thi Hoang</au><au>Reis, Marcus H</au><au>Qi, Pengxu</au><au>Miller, Stephen A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2015-01-01</date><risdate>2015</risdate><volume>17</volume><issue>9</issue><spage>4512</spage><epage>4517</epage><pages>4512-4517</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>Ferulic acid and p-coumaric acid are abundant, biorenewable precursors for the synthesis of polyethylene ferulate (PEF) and polyethylene coumarate (PEC), as well as cognate copolymers with prescribed hydrogenation of the main-chain double bond. By controlling the comonomer feed ratios, copolymers with tunable thermal properties are obtained, including the thermal range occupied by polystyrene (PS).</abstract><doi>10.1039/c5gc01104c</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1463-9262
ispartof Green chemistry : an international journal and green chemistry resource : GC, 2015-01, Vol.17 (9), p.4512-4517
issn 1463-9262
1463-9270
language eng
recordid cdi_proquest_miscellaneous_1744710419
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Bonding
Congeners
Copolymers
Hydrogenation
Polyethylenes
Polystyrene resins
Precursors
Thermal properties
title Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T09%3A17%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Polyethylene%20ferulate%20(PEF)%20and%20congeners:%20polystyrene%20mimics%20derived%20from%20biorenewable%20aromatics&rft.jtitle=Green%20chemistry%20:%20an%20international%20journal%20and%20green%20chemistry%20resource%20:%20GC&rft.au=Nguyen,%20Ha%20Thi%20Hoang&rft.date=2015-01-01&rft.volume=17&rft.issue=9&rft.spage=4512&rft.epage=4517&rft.pages=4512-4517&rft.issn=1463-9262&rft.eissn=1463-9270&rft_id=info:doi/10.1039/c5gc01104c&rft_dat=%3Cproquest_cross%3E1712774010%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1712774010&rft_id=info:pmid/&rfr_iscdi=true