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Synthesis of block copolymers via redox polymerization
Polymerization and copolymerization of vinyl monomers such as acrylamide, acrylonitrile, vinyl acetate, and acrylic acid with a redox system of Ce(IV) and organic reducing agents containing hydroxy groups were studied. The reducing compounds were poly(ethylene glycol)s, halogen‐containing polyols, a...
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Published in: | Journal of applied polymer science 1999-02, Vol.71 (9), p.1385-1395 |
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creator | Atici, Oya Gali̇oğlu Akar, Ahmet Ayar, Yusuf Meci̇t, Oğuz |
description | Polymerization and copolymerization of vinyl monomers such as acrylamide, acrylonitrile, vinyl acetate, and acrylic acid with a redox system of Ce(IV) and organic reducing agents containing hydroxy groups were studied. The reducing compounds were poly(ethylene glycol)s, halogen‐containing polyols, and depolymerization products of poly(ethylene terephthalate). Copolymers of poly(ethylene glycol)s‐b‐polyacrylonitrile, poly(ethylene glycol)s‐b‐poly(acrylonitrile‐co‐vinyl acetate), poly(ethylene glycol)s‐b‐polyacrylamide, poly(ethylene glycol)s‐b‐poly(acrylamide‐co‐vinyl acetate), poly(1‐chloromethyl ethylene glycol)‐bpoly(acrylonitrile‐co‐vinyl acetate), and bis[poly(ethylene glycol terephthalate)]‐b‐poly(acrylonitrile‐co‐vinyl acetate) were produced. The yield of acrylamide polymerization and the molecular weight of the copolymer increased considerably if about 4% vinyl acetate was added into the acrylamide monomer. However, the molecular weight of the copolymer was decreased when 4% vinyl acetate was added into the acrylonitrile monomer. Physical properties such as solubility, water absorption, resistance to UV light, and viscosities of the copolymers were studied and their possible uses are discussed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1385–1395, 1999 |
doi_str_mv | 10.1002/(SICI)1097-4628(19990228)71:9<1385::AID-APP4>3.0.CO;2-F |
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The reducing compounds were poly(ethylene glycol)s, halogen‐containing polyols, and depolymerization products of poly(ethylene terephthalate). Copolymers of poly(ethylene glycol)s‐b‐polyacrylonitrile, poly(ethylene glycol)s‐b‐poly(acrylonitrile‐co‐vinyl acetate), poly(ethylene glycol)s‐b‐polyacrylamide, poly(ethylene glycol)s‐b‐poly(acrylamide‐co‐vinyl acetate), poly(1‐chloromethyl ethylene glycol)‐bpoly(acrylonitrile‐co‐vinyl acetate), and bis[poly(ethylene glycol terephthalate)]‐b‐poly(acrylonitrile‐co‐vinyl acetate) were produced. The yield of acrylamide polymerization and the molecular weight of the copolymer increased considerably if about 4% vinyl acetate was added into the acrylamide monomer. However, the molecular weight of the copolymer was decreased when 4% vinyl acetate was added into the acrylonitrile monomer. Physical properties such as solubility, water absorption, resistance to UV light, and viscosities of the copolymers were studied and their possible uses are discussed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1385–1395, 1999</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/(SICI)1097-4628(19990228)71:9<1385::AID-APP4>3.0.CO;2-F</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>acrylamide ; acrylonitrile ; Applied sciences ; block copolymers ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; poly(ethylene glycol)s ; Polymerization ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; redox polymerization</subject><ispartof>Journal of applied polymer science, 1999-02, Vol.71 (9), p.1385-1395</ispartof><rights>Copyright © 1999 John Wiley & Sons, Inc.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4114-cca7b50ab420036dc06b716c5ad5f40fa553b0e74a6e1388257195c43e64f2883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1638292$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Atici, Oya Gali̇oğlu</creatorcontrib><creatorcontrib>Akar, Ahmet</creatorcontrib><creatorcontrib>Ayar, Yusuf</creatorcontrib><creatorcontrib>Meci̇t, Oğuz</creatorcontrib><title>Synthesis of block copolymers via redox polymerization</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>Polymerization and copolymerization of vinyl monomers such as acrylamide, acrylonitrile, vinyl acetate, and acrylic acid with a redox system of Ce(IV) and organic reducing agents containing hydroxy groups were studied. The reducing compounds were poly(ethylene glycol)s, halogen‐containing polyols, and depolymerization products of poly(ethylene terephthalate). Copolymers of poly(ethylene glycol)s‐b‐polyacrylonitrile, poly(ethylene glycol)s‐b‐poly(acrylonitrile‐co‐vinyl acetate), poly(ethylene glycol)s‐b‐polyacrylamide, poly(ethylene glycol)s‐b‐poly(acrylamide‐co‐vinyl acetate), poly(1‐chloromethyl ethylene glycol)‐bpoly(acrylonitrile‐co‐vinyl acetate), and bis[poly(ethylene glycol terephthalate)]‐b‐poly(acrylonitrile‐co‐vinyl acetate) were produced. The yield of acrylamide polymerization and the molecular weight of the copolymer increased considerably if about 4% vinyl acetate was added into the acrylamide monomer. However, the molecular weight of the copolymer was decreased when 4% vinyl acetate was added into the acrylonitrile monomer. Physical properties such as solubility, water absorption, resistance to UV light, and viscosities of the copolymers were studied and their possible uses are discussed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1385–1395, 1999</description><subject>acrylamide</subject><subject>acrylonitrile</subject><subject>Applied sciences</subject><subject>block copolymers</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>poly(ethylene glycol)s</subject><subject>Polymerization</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>redox polymerization</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkE1vEzEQhi0EEqHwH_aAUHvY4O-PgEDRQkpQIEEFFXEZeR2vcLuJg51Cw69nl4T2ABIna6yZ5515EHpJ8JBgTJ8en02r6QnBRpVcUn1MjDGYUn2iyMg8J0yL0Wg8fVWOFwv-gg3xsJo_o-XkDhrczNxFg45ESm2MuI8e5HyBMSECywGSZ7v19qvPIRexKeo2usvCxU1sdyufcvE92CL5ZbwuDl_hp92GuH6I7jW2zf7R4T1CnyavP1Zvytn8dFqNZ6XjhPDSOatqgW3NKcZMLh2WtSLSCbsUDceNFYLV2Ctupe8u0VQoYoTjzEveUK3ZEXqy525S_Hbl8xZWITvftnbt41UG2tEk16ZrPN83uhRzTr6BTQorm3ZAMPQeAXqP0DuB3gn88QiKgIHeI0DnEXqPwABDNQcKk478-LCCzc62TbJrF_ItXjJNDb1d4Edo_e6v9P-H_yP7d92Ryz055K2_viHbdAlSMSXg_P0pLD6o2ecvk7fwjv0CbtihWw</recordid><startdate>19990228</startdate><enddate>19990228</enddate><creator>Atici, Oya Gali̇oğlu</creator><creator>Akar, Ahmet</creator><creator>Ayar, Yusuf</creator><creator>Meci̇t, Oğuz</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>19990228</creationdate><title>Synthesis of block copolymers via redox polymerization</title><author>Atici, Oya Gali̇oğlu ; Akar, Ahmet ; Ayar, Yusuf ; Meci̇t, Oğuz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4114-cca7b50ab420036dc06b716c5ad5f40fa553b0e74a6e1388257195c43e64f2883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>acrylamide</topic><topic>acrylonitrile</topic><topic>Applied sciences</topic><topic>block copolymers</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>poly(ethylene glycol)s</topic><topic>Polymerization</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>redox polymerization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Atici, Oya Gali̇oğlu</creatorcontrib><creatorcontrib>Akar, Ahmet</creatorcontrib><creatorcontrib>Ayar, Yusuf</creatorcontrib><creatorcontrib>Meci̇t, Oğuz</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Atici, Oya Gali̇oğlu</au><au>Akar, Ahmet</au><au>Ayar, Yusuf</au><au>Meci̇t, Oğuz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of block copolymers via redox polymerization</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>1999-02-28</date><risdate>1999</risdate><volume>71</volume><issue>9</issue><spage>1385</spage><epage>1395</epage><pages>1385-1395</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>Polymerization and copolymerization of vinyl monomers such as acrylamide, acrylonitrile, vinyl acetate, and acrylic acid with a redox system of Ce(IV) and organic reducing agents containing hydroxy groups were studied. The reducing compounds were poly(ethylene glycol)s, halogen‐containing polyols, and depolymerization products of poly(ethylene terephthalate). Copolymers of poly(ethylene glycol)s‐b‐polyacrylonitrile, poly(ethylene glycol)s‐b‐poly(acrylonitrile‐co‐vinyl acetate), poly(ethylene glycol)s‐b‐polyacrylamide, poly(ethylene glycol)s‐b‐poly(acrylamide‐co‐vinyl acetate), poly(1‐chloromethyl ethylene glycol)‐bpoly(acrylonitrile‐co‐vinyl acetate), and bis[poly(ethylene glycol terephthalate)]‐b‐poly(acrylonitrile‐co‐vinyl acetate) were produced. The yield of acrylamide polymerization and the molecular weight of the copolymer increased considerably if about 4% vinyl acetate was added into the acrylamide monomer. However, the molecular weight of the copolymer was decreased when 4% vinyl acetate was added into the acrylonitrile monomer. Physical properties such as solubility, water absorption, resistance to UV light, and viscosities of the copolymers were studied and their possible uses are discussed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1385–1395, 1999</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/(SICI)1097-4628(19990228)71:9<1385::AID-APP4>3.0.CO;2-F</doi><tpages>11</tpages></addata></record> |
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subjects | acrylamide acrylonitrile Applied sciences block copolymers Exact sciences and technology Organic polymers Physicochemistry of polymers poly(ethylene glycol)s Polymerization Preparation, kinetics, thermodynamics, mechanism and catalysts redox polymerization |
title | Synthesis of block copolymers via redox polymerization |
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