Synthesis of novel maleimide-terminated thioetherimide oligomer and its bulk copolymerization with reactive solvents
This paper reports the synthesis of a novel maleimide-terminated thioetherimide oligomer and its copolymerization with reactive solvents bearing vinyl. Starting from 3-chlorophthalic anhydride and 4-chlorophthalic anhydride, 2,2′,3,3′-thiodiphenyl tertracaboxylic dianhydride (3,3′-TDPA) and 3,3′,4,4...
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Veröffentlicht in: | Polymer (Guilford) 2006-01, Vol.47 (3), p.937-945 |
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description | This paper reports the synthesis of a novel maleimide-terminated thioetherimide oligomer and its copolymerization with reactive solvents bearing vinyl. Starting from 3-chlorophthalic anhydride and 4-chlorophthalic anhydride, 2,2′,3,3′-thiodiphenyl tertracaboxylic dianhydride (3,3′-TDPA) and 3,3′,4,4′-thiodiphenyl tertracaboxylic dianhydride (4,4′-TDPA) were synthesized. Thereby, a novel maleimide-terminated thioetherimide oligomer was prepared from. 3,3′-TDPA, 4,4′-TDPA, 3,3′-dimethyl-4,4′-diaminodiphenylmethane (DMMDA) and maleic anhydride. Binary and ternary copolymer resin were derived from corresponding binary and ternary homogeous solution consisting of thioetherimide oligomer, reactive solvent
N-vinylpyrrolidone (NVP) or
N,
N′-dimethylacrylamide (DMAA) and divinylbenzene (DVB) as modifier, initiated either by gamma ray irradiation or by benzoyl peroxide (BPO). Thermal and mechanical properties of copolymer resin are determined and compared in terms of the kind of reactive solvent, addition of modifier DVB. The effect of initiation approach on property of final copolymer resin were studied. Phase separation and sub-transition of ternary copolymer resin induced by BPO are observed, which could be accounted for by thermal movement of DMAA molecules during thermal initiation. Structure-property relationship of copolymer resin was discussed. The effect of monomer molar ratio of 3,3′-TDPA and 4,4′-TDPA on thermal and mechanical properties were investigated. |
doi_str_mv | 10.1016/j.polymer.2005.12.001 |
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N-vinylpyrrolidone (NVP) or
N,
N′-dimethylacrylamide (DMAA) and divinylbenzene (DVB) as modifier, initiated either by gamma ray irradiation or by benzoyl peroxide (BPO). Thermal and mechanical properties of copolymer resin are determined and compared in terms of the kind of reactive solvent, addition of modifier DVB. The effect of initiation approach on property of final copolymer resin were studied. Phase separation and sub-transition of ternary copolymer resin induced by BPO are observed, which could be accounted for by thermal movement of DMAA molecules during thermal initiation. Structure-property relationship of copolymer resin was discussed. The effect of monomer molar ratio of 3,3′-TDPA and 4,4′-TDPA on thermal and mechanical properties were investigated.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2005.12.001</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Exact sciences and technology ; Isomeric effects ; Maleimide-terminated thioetherimide oligomer ; Organic polymers ; Physicochemistry of polymers ; Polycondensation ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Reactive solvents</subject><ispartof>Polymer (Guilford), 2006-01, Vol.47 (3), p.937-945</ispartof><rights>2005 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-a59c072697e4053cefaa82cd16c8a0d035a7b0ec911aa1b226901665f191c2603</citedby><cites>FETCH-LOGICAL-c370t-a59c072697e4053cefaa82cd16c8a0d035a7b0ec911aa1b226901665f191c2603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.polymer.2005.12.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17408057$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Feng</creatorcontrib><creatorcontrib>Wang, Zhen</creatorcontrib><creatorcontrib>Yang, Huili</creatorcontrib><creatorcontrib>Gao, Lianxun</creatorcontrib><creatorcontrib>Ding, Mengxian</creatorcontrib><title>Synthesis of novel maleimide-terminated thioetherimide oligomer and its bulk copolymerization with reactive solvents</title><title>Polymer (Guilford)</title><description>This paper reports the synthesis of a novel maleimide-terminated thioetherimide oligomer and its copolymerization with reactive solvents bearing vinyl. Starting from 3-chlorophthalic anhydride and 4-chlorophthalic anhydride, 2,2′,3,3′-thiodiphenyl tertracaboxylic dianhydride (3,3′-TDPA) and 3,3′,4,4′-thiodiphenyl tertracaboxylic dianhydride (4,4′-TDPA) were synthesized. Thereby, a novel maleimide-terminated thioetherimide oligomer was prepared from. 3,3′-TDPA, 4,4′-TDPA, 3,3′-dimethyl-4,4′-diaminodiphenylmethane (DMMDA) and maleic anhydride. Binary and ternary copolymer resin were derived from corresponding binary and ternary homogeous solution consisting of thioetherimide oligomer, reactive solvent
N-vinylpyrrolidone (NVP) or
N,
N′-dimethylacrylamide (DMAA) and divinylbenzene (DVB) as modifier, initiated either by gamma ray irradiation or by benzoyl peroxide (BPO). Thermal and mechanical properties of copolymer resin are determined and compared in terms of the kind of reactive solvent, addition of modifier DVB. The effect of initiation approach on property of final copolymer resin were studied. Phase separation and sub-transition of ternary copolymer resin induced by BPO are observed, which could be accounted for by thermal movement of DMAA molecules during thermal initiation. Structure-property relationship of copolymer resin was discussed. The effect of monomer molar ratio of 3,3′-TDPA and 4,4′-TDPA on thermal and mechanical properties were investigated.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Isomeric effects</subject><subject>Maleimide-terminated thioetherimide oligomer</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polycondensation</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Reactive solvents</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkE1vEzEQhi1EJULLT0DyBW67jL3ZrxNCFQWkShygZ2vinSUTvHawnaD01-OSSBw5-TDPzOv3EeK1glqB6t7t6n1wp4VirQHaWukaQD0TKzX0TaX1qJ6LFUCjq2bo1AvxMqUdAOhWr1cifzv5vKXESYZZ-nAkJxd0xAtPVGWKC3vMNMm85UCFjH8nMjj-EUqkRD9JzkluDu6ntOHyE37EzMHL35y3MhLazEeSKbgj-ZxuxNWMLtGry3stHu4-fr_9XN1__fTl9sN9ZZsecoXtaKHX3djTGtrG0ow4aDupzg4IEzQt9hsgOyqFqDa6kEVH185qVFZ30FyLt-e7-xh-HShls3Cy5Bx6Codk9NBrVQQVsD2DNoaUIs1mX3piPBkF5smx2ZlLM_Pk2ChtiuOy9-YSgMmimyN6y-nfcr-GAdq-cO_PHJW2Ry5XkmXyliaOZLOZAv8n6Q9yHZgk</recordid><startdate>20060125</startdate><enddate>20060125</enddate><creator>Liu, Feng</creator><creator>Wang, Zhen</creator><creator>Yang, Huili</creator><creator>Gao, Lianxun</creator><creator>Ding, Mengxian</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>20060125</creationdate><title>Synthesis of novel maleimide-terminated thioetherimide oligomer and its bulk copolymerization with reactive solvents</title><author>Liu, Feng ; Wang, Zhen ; Yang, Huili ; Gao, Lianxun ; Ding, Mengxian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-a59c072697e4053cefaa82cd16c8a0d035a7b0ec911aa1b226901665f191c2603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Isomeric effects</topic><topic>Maleimide-terminated thioetherimide oligomer</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polycondensation</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Reactive solvents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Feng</creatorcontrib><creatorcontrib>Wang, Zhen</creatorcontrib><creatorcontrib>Yang, Huili</creatorcontrib><creatorcontrib>Gao, Lianxun</creatorcontrib><creatorcontrib>Ding, Mengxian</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Feng</au><au>Wang, Zhen</au><au>Yang, Huili</au><au>Gao, Lianxun</au><au>Ding, Mengxian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of novel maleimide-terminated thioetherimide oligomer and its bulk copolymerization with reactive solvents</atitle><jtitle>Polymer (Guilford)</jtitle><date>2006-01-25</date><risdate>2006</risdate><volume>47</volume><issue>3</issue><spage>937</spage><epage>945</epage><pages>937-945</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>This paper reports the synthesis of a novel maleimide-terminated thioetherimide oligomer and its copolymerization with reactive solvents bearing vinyl. Starting from 3-chlorophthalic anhydride and 4-chlorophthalic anhydride, 2,2′,3,3′-thiodiphenyl tertracaboxylic dianhydride (3,3′-TDPA) and 3,3′,4,4′-thiodiphenyl tertracaboxylic dianhydride (4,4′-TDPA) were synthesized. Thereby, a novel maleimide-terminated thioetherimide oligomer was prepared from. 3,3′-TDPA, 4,4′-TDPA, 3,3′-dimethyl-4,4′-diaminodiphenylmethane (DMMDA) and maleic anhydride. Binary and ternary copolymer resin were derived from corresponding binary and ternary homogeous solution consisting of thioetherimide oligomer, reactive solvent
N-vinylpyrrolidone (NVP) or
N,
N′-dimethylacrylamide (DMAA) and divinylbenzene (DVB) as modifier, initiated either by gamma ray irradiation or by benzoyl peroxide (BPO). Thermal and mechanical properties of copolymer resin are determined and compared in terms of the kind of reactive solvent, addition of modifier DVB. The effect of initiation approach on property of final copolymer resin were studied. Phase separation and sub-transition of ternary copolymer resin induced by BPO are observed, which could be accounted for by thermal movement of DMAA molecules during thermal initiation. Structure-property relationship of copolymer resin was discussed. The effect of monomer molar ratio of 3,3′-TDPA and 4,4′-TDPA on thermal and mechanical properties were investigated.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2005.12.001</doi><tpages>9</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Isomeric effects Maleimide-terminated thioetherimide oligomer Organic polymers Physicochemistry of polymers Polycondensation Preparation, kinetics, thermodynamics, mechanism and catalysts Reactive solvents |
title | Synthesis of novel maleimide-terminated thioetherimide oligomer and its bulk copolymerization with reactive solvents |
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