Functionalisation of Polyolefins: Grafting of Phenol Groups on Olefin/5,7-Dimethylocta-1,6-diene Copolymers
The grafting of phenol groups on ethylene/5,7‐dimethylocta‐1,6‐diene copolymers and on ethylene/propylene/5,7‐dimethylocta‐1,6‐diene terpolymers was performed, using two different modification procedures. An indirect route involving hydrochlorination followed by phenol insertion was found to be very...
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Veröffentlicht in: | Macromolecular chemistry and physics 2003-10, Vol.204 (15), p.1889-1897 |
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container_end_page | 1897 |
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container_issue | 15 |
container_start_page | 1889 |
container_title | Macromolecular chemistry and physics |
container_volume | 204 |
creator | Dolatkhani, Marc Cramail, Henri Deffieux, Alain Santos, Jorge Moniz Ribeiro, Maria Rosário Bordado, João M. |
description | The grafting of phenol groups on ethylene/5,7‐dimethylocta‐1,6‐diene copolymers and on ethylene/propylene/5,7‐dimethylocta‐1,6‐diene terpolymers was performed, using two different modification procedures. An indirect route involving hydrochlorination followed by phenol insertion was found to be very effective for the terpolymers, and lead to a grafting phenol rate higher than 75%. However, if the phenol grafting is performed directly on a non‐modified terpolymer, lower rates are obtained. When applied to the copolymers the procedures used were revealed to be less efficient. This fact might be related to the lower solubility of the ethylene/5,7‐dimethylocta‐1,6‐diene copolymers (related to a higher crystallinity and a smaller diene content) when compared with the corresponding terpolymers. Although incomplete, the addition of a hindered phenol to the copolymer gave rise to a polymer that, when compared to polyethylene, presents a higher thermal‐oxidative stability.
Grafting of phenol on a hydrochlorinated ethylene/propylene/5,7‐DMO terpolymer. |
doi_str_mv | 10.1002/macp.200350045 |
format | Article |
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Grafting of phenol on a hydrochlorinated ethylene/propylene/5,7‐DMO terpolymer.</description><identifier>ISSN: 1022-1352</identifier><identifier>EISSN: 1521-3935</identifier><identifier>DOI: 10.1002/macp.200350045</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>antioxidants ; Applied sciences ; Chemical modifications ; Chemical reactions and properties ; EPDM ; Exact sciences and technology ; functionalization of polymers ; non-conjugated dienes ; Organic polymers ; Physicochemistry of polymers ; polyolefins</subject><ispartof>Macromolecular chemistry and physics, 2003-10, Vol.204 (15), p.1889-1897</ispartof><rights>Copyright © 2003 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3555-b71cf5a2ea761d67a3df86abbbc82cc39ae8daddcef8a42ae37c856b8ba437d3</citedby><cites>FETCH-LOGICAL-c3555-b71cf5a2ea761d67a3df86abbbc82cc39ae8daddcef8a42ae37c856b8ba437d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmacp.200350045$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmacp.200350045$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15258366$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Dolatkhani, Marc</creatorcontrib><creatorcontrib>Cramail, Henri</creatorcontrib><creatorcontrib>Deffieux, Alain</creatorcontrib><creatorcontrib>Santos, Jorge Moniz</creatorcontrib><creatorcontrib>Ribeiro, Maria Rosário</creatorcontrib><creatorcontrib>Bordado, João M.</creatorcontrib><title>Functionalisation of Polyolefins: Grafting of Phenol Groups on Olefin/5,7-Dimethylocta-1,6-diene Copolymers</title><title>Macromolecular chemistry and physics</title><addtitle>Macromol. Chem. Phys</addtitle><description>The grafting of phenol groups on ethylene/5,7‐dimethylocta‐1,6‐diene copolymers and on ethylene/propylene/5,7‐dimethylocta‐1,6‐diene terpolymers was performed, using two different modification procedures. An indirect route involving hydrochlorination followed by phenol insertion was found to be very effective for the terpolymers, and lead to a grafting phenol rate higher than 75%. However, if the phenol grafting is performed directly on a non‐modified terpolymer, lower rates are obtained. When applied to the copolymers the procedures used were revealed to be less efficient. This fact might be related to the lower solubility of the ethylene/5,7‐dimethylocta‐1,6‐diene copolymers (related to a higher crystallinity and a smaller diene content) when compared with the corresponding terpolymers. Although incomplete, the addition of a hindered phenol to the copolymer gave rise to a polymer that, when compared to polyethylene, presents a higher thermal‐oxidative stability.
Grafting of phenol on a hydrochlorinated ethylene/propylene/5,7‐DMO terpolymer.</description><subject>antioxidants</subject><subject>Applied sciences</subject><subject>Chemical modifications</subject><subject>Chemical reactions and properties</subject><subject>EPDM</subject><subject>Exact sciences and technology</subject><subject>functionalization of polymers</subject><subject>non-conjugated dienes</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>polyolefins</subject><issn>1022-1352</issn><issn>1521-3935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkL1PwzAQxSMEElBYmbOw4dYfdeywoUBbpPIxVDBaF8emhiSO4lTQ_560RYWN6Z7u3u-d9KLoguAhwZiOKtDNkGLMOMZjfhCdEE4JYinjh73GlCLCOD2OTkN4xxhLnIqT6GOyqnXnfA2lC7ARsbfxsy_XvjTW1eE6nrZgO1e_bQ9LU_uyX_lVE-Le_LR1jfiVQLeuMt1yXXrdASJXCSqcqU2c-aZPq0wbzqIjC2Uw5z9zEC0md4tshuZP0_vsZo4045yjXBBtOVADIiFFIoAVViaQ57mWVGuWgpEFFIU2VsKYgmFCS57kMocxEwUbRMNdrG59CK2xqmldBe1aEaw2TalNU2rfVA9c7oAGgobStlBrF34pTrlkSdL70p3v05Vm_U-qerjJnv_-QDvWhc587VloP1QimODq9XGq6Oz1UeJFpl7YN-qii5Q</recordid><startdate>200310</startdate><enddate>200310</enddate><creator>Dolatkhani, Marc</creator><creator>Cramail, Henri</creator><creator>Deffieux, Alain</creator><creator>Santos, Jorge Moniz</creator><creator>Ribeiro, Maria Rosário</creator><creator>Bordado, João M.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200310</creationdate><title>Functionalisation of Polyolefins: Grafting of Phenol Groups on Olefin/5,7-Dimethylocta-1,6-diene Copolymers</title><author>Dolatkhani, Marc ; Cramail, Henri ; Deffieux, Alain ; Santos, Jorge Moniz ; Ribeiro, Maria Rosário ; Bordado, João M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3555-b71cf5a2ea761d67a3df86abbbc82cc39ae8daddcef8a42ae37c856b8ba437d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>antioxidants</topic><topic>Applied sciences</topic><topic>Chemical modifications</topic><topic>Chemical reactions and properties</topic><topic>EPDM</topic><topic>Exact sciences and technology</topic><topic>functionalization of polymers</topic><topic>non-conjugated dienes</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>polyolefins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dolatkhani, Marc</creatorcontrib><creatorcontrib>Cramail, Henri</creatorcontrib><creatorcontrib>Deffieux, Alain</creatorcontrib><creatorcontrib>Santos, Jorge Moniz</creatorcontrib><creatorcontrib>Ribeiro, Maria Rosário</creatorcontrib><creatorcontrib>Bordado, João M.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecular chemistry and physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dolatkhani, Marc</au><au>Cramail, Henri</au><au>Deffieux, Alain</au><au>Santos, Jorge Moniz</au><au>Ribeiro, Maria Rosário</au><au>Bordado, João M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functionalisation of Polyolefins: Grafting of Phenol Groups on Olefin/5,7-Dimethylocta-1,6-diene Copolymers</atitle><jtitle>Macromolecular chemistry and physics</jtitle><addtitle>Macromol. Chem. Phys</addtitle><date>2003-10</date><risdate>2003</risdate><volume>204</volume><issue>15</issue><spage>1889</spage><epage>1897</epage><pages>1889-1897</pages><issn>1022-1352</issn><eissn>1521-3935</eissn><abstract>The grafting of phenol groups on ethylene/5,7‐dimethylocta‐1,6‐diene copolymers and on ethylene/propylene/5,7‐dimethylocta‐1,6‐diene terpolymers was performed, using two different modification procedures. An indirect route involving hydrochlorination followed by phenol insertion was found to be very effective for the terpolymers, and lead to a grafting phenol rate higher than 75%. However, if the phenol grafting is performed directly on a non‐modified terpolymer, lower rates are obtained. When applied to the copolymers the procedures used were revealed to be less efficient. This fact might be related to the lower solubility of the ethylene/5,7‐dimethylocta‐1,6‐diene copolymers (related to a higher crystallinity and a smaller diene content) when compared with the corresponding terpolymers. Although incomplete, the addition of a hindered phenol to the copolymer gave rise to a polymer that, when compared to polyethylene, presents a higher thermal‐oxidative stability.
Grafting of phenol on a hydrochlorinated ethylene/propylene/5,7‐DMO terpolymer.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/macp.200350045</doi><tpages>9</tpages></addata></record> |
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subjects | antioxidants Applied sciences Chemical modifications Chemical reactions and properties EPDM Exact sciences and technology functionalization of polymers non-conjugated dienes Organic polymers Physicochemistry of polymers polyolefins |
title | Functionalisation of Polyolefins: Grafting of Phenol Groups on Olefin/5,7-Dimethylocta-1,6-diene Copolymers |
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