s-Triazine-based functional monomers with thermocrosslinkable propargyl units: Synthesis and conversion to the heat-resistant polymers

Three s-triazine-based functional monomers with thermo-polymerizable propargyl-ether units were synthesized by a facile procedure. These monomers can be thermally cured to form the crosslinked networks, which showed 5-wt% loss temperature of up to 400 °C and the char yields of more than 50% at 1000 ...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Polymer (Guilford) 2016-10, Vol.102, p.301-307
Hauptverfasser: Zhou, Junfeng, Wang, Jiajia, Jin, Kaikai, Sun, Jing, Fang, Qiang
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 307
container_issue
container_start_page 301
container_title Polymer (Guilford)
container_volume 102
creator Zhou, Junfeng
Wang, Jiajia
Jin, Kaikai
Sun, Jing
Fang, Qiang
description Three s-triazine-based functional monomers with thermo-polymerizable propargyl-ether units were synthesized by a facile procedure. These monomers can be thermally cured to form the crosslinked networks, which showed 5-wt% loss temperature of up to 400 °C and the char yields of more than 50% at 1000 °C. Moreover, the crosslinked networks exhibited the coefficients of thermal expansion (CTE) of below 43 ppm °C−1 varying from 30 to 300 °C and glass transition temperatures (Tg) of up to 290 °C, respectively. These monomers were also used to improve the thermostability of a commercial bismaleimide (4,4′-bismaleimidodiphenylmethane). The results indicated that blending the bismaleimide and the triazine monomers gave the new resins, which showed higher Tg and lower CTE than the bismaleimide, suggesting the triazine monomers can be considered as the modifiers for enhancement of the thermostability of the commercial bismaleimides. s-Triazine-based functional monomers with thermo-polymerizable propargyl-ether units are reported here. Thermopolymerization of the monomers gave the crosslinked networks, showing high low coefficients of thermal expansion (CTE) high glass transition temperatures (Tg). These monomers were also used to improve the properties of a commercial bismaleimide, producing the copolymers with the better thermostability than that the neat bismaleimide. [Display omitted]
doi_str_mv 10.1016/j.polymer.2016.09.027
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1845807865</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0032386116308266</els_id><sourcerecordid>1845807865</sourcerecordid><originalsourceid>FETCH-LOGICAL-c342t-761cb30274fcd5acc73f2af9d379173a5408e6945b71dff7bda19814816b2fdf3</originalsourceid><addsrcrecordid>eNqFkMtOwzAQRS0EEqXwCUhesknwI4kTNghVvCQkFsDacvygLoldbLeofADfjUu7ZzUazb1H9w4A5xiVGOHmclEu_bAZdShJXkvUlYiwAzDBLaMFIR0-BBOEKClo2-BjcBLjAiFEalJNwE8sXoMV39bpohdRK2hWTibrnRjg6J3P2Ai_bJrDNNdh9DL4GAfrPkQ_aLgMfinC-2aAK2dTvIIvG5d10UYonILSu3X2ZxpMfguAcy1SEbaCJFyC--DxFBwZMUR9tp9T8HZ3-zp7KJ6e7x9nN0-FpBVJBWuw7GluVxmpaiElo4YI0ynKOsyoqCvU6qar6p5hZQzrlcBdi6sWNz0xytApuNhxc_DPlY6JjzZKPQzCab-KHLdV3SLWNnWW1jvpX-OgDV8GO4qw4Rjx7d_5gu_j8-3fOep4TpZ91zufzj3WNl-jtNpJrWzQMnHl7T-EXyS-k7s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1845807865</pqid></control><display><type>article</type><title>s-Triazine-based functional monomers with thermocrosslinkable propargyl units: Synthesis and conversion to the heat-resistant polymers</title><source>Elsevier ScienceDirect Journals</source><creator>Zhou, Junfeng ; Wang, Jiajia ; Jin, Kaikai ; Sun, Jing ; Fang, Qiang</creator><creatorcontrib>Zhou, Junfeng ; Wang, Jiajia ; Jin, Kaikai ; Sun, Jing ; Fang, Qiang</creatorcontrib><description>Three s-triazine-based functional monomers with thermo-polymerizable propargyl-ether units were synthesized by a facile procedure. These monomers can be thermally cured to form the crosslinked networks, which showed 5-wt% loss temperature of up to 400 °C and the char yields of more than 50% at 1000 °C. Moreover, the crosslinked networks exhibited the coefficients of thermal expansion (CTE) of below 43 ppm °C−1 varying from 30 to 300 °C and glass transition temperatures (Tg) of up to 290 °C, respectively. These monomers were also used to improve the thermostability of a commercial bismaleimide (4,4′-bismaleimidodiphenylmethane). The results indicated that blending the bismaleimide and the triazine monomers gave the new resins, which showed higher Tg and lower CTE than the bismaleimide, suggesting the triazine monomers can be considered as the modifiers for enhancement of the thermostability of the commercial bismaleimides. s-Triazine-based functional monomers with thermo-polymerizable propargyl-ether units are reported here. Thermopolymerization of the monomers gave the crosslinked networks, showing high low coefficients of thermal expansion (CTE) high glass transition temperatures (Tg). These monomers were also used to improve the properties of a commercial bismaleimide, producing the copolymers with the better thermostability than that the neat bismaleimide. [Display omitted]</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2016.09.027</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Bismaleimides ; Blending ; Conversion ; Crosslinking ; Functional polymers ; Heat-resistant polymers ; Monomers ; Propargyl ; s-Triazine ; Synthesis ; Thermal stability ; Thermostability ; Transportation networks</subject><ispartof>Polymer (Guilford), 2016-10, Vol.102, p.301-307</ispartof><rights>2016 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-761cb30274fcd5acc73f2af9d379173a5408e6945b71dff7bda19814816b2fdf3</citedby><cites>FETCH-LOGICAL-c342t-761cb30274fcd5acc73f2af9d379173a5408e6945b71dff7bda19814816b2fdf3</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.2016.09.027$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids></links><search><creatorcontrib>Zhou, Junfeng</creatorcontrib><creatorcontrib>Wang, Jiajia</creatorcontrib><creatorcontrib>Jin, Kaikai</creatorcontrib><creatorcontrib>Sun, Jing</creatorcontrib><creatorcontrib>Fang, Qiang</creatorcontrib><title>s-Triazine-based functional monomers with thermocrosslinkable propargyl units: Synthesis and conversion to the heat-resistant polymers</title><title>Polymer (Guilford)</title><description>Three s-triazine-based functional monomers with thermo-polymerizable propargyl-ether units were synthesized by a facile procedure. These monomers can be thermally cured to form the crosslinked networks, which showed 5-wt% loss temperature of up to 400 °C and the char yields of more than 50% at 1000 °C. Moreover, the crosslinked networks exhibited the coefficients of thermal expansion (CTE) of below 43 ppm °C−1 varying from 30 to 300 °C and glass transition temperatures (Tg) of up to 290 °C, respectively. These monomers were also used to improve the thermostability of a commercial bismaleimide (4,4′-bismaleimidodiphenylmethane). The results indicated that blending the bismaleimide and the triazine monomers gave the new resins, which showed higher Tg and lower CTE than the bismaleimide, suggesting the triazine monomers can be considered as the modifiers for enhancement of the thermostability of the commercial bismaleimides. s-Triazine-based functional monomers with thermo-polymerizable propargyl-ether units are reported here. Thermopolymerization of the monomers gave the crosslinked networks, showing high low coefficients of thermal expansion (CTE) high glass transition temperatures (Tg). These monomers were also used to improve the properties of a commercial bismaleimide, producing the copolymers with the better thermostability than that the neat bismaleimide. [Display omitted]</description><subject>Bismaleimides</subject><subject>Blending</subject><subject>Conversion</subject><subject>Crosslinking</subject><subject>Functional polymers</subject><subject>Heat-resistant polymers</subject><subject>Monomers</subject><subject>Propargyl</subject><subject>s-Triazine</subject><subject>Synthesis</subject><subject>Thermal stability</subject><subject>Thermostability</subject><subject>Transportation networks</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EEqXwCUhesknwI4kTNghVvCQkFsDacvygLoldbLeofADfjUu7ZzUazb1H9w4A5xiVGOHmclEu_bAZdShJXkvUlYiwAzDBLaMFIR0-BBOEKClo2-BjcBLjAiFEalJNwE8sXoMV39bpohdRK2hWTibrnRjg6J3P2Ai_bJrDNNdh9DL4GAfrPkQ_aLgMfinC-2aAK2dTvIIvG5d10UYonILSu3X2ZxpMfguAcy1SEbaCJFyC--DxFBwZMUR9tp9T8HZ3-zp7KJ6e7x9nN0-FpBVJBWuw7GluVxmpaiElo4YI0ynKOsyoqCvU6qar6p5hZQzrlcBdi6sWNz0xytApuNhxc_DPlY6JjzZKPQzCab-KHLdV3SLWNnWW1jvpX-OgDV8GO4qw4Rjx7d_5gu_j8-3fOep4TpZ91zufzj3WNl-jtNpJrWzQMnHl7T-EXyS-k7s</recordid><startdate>20161012</startdate><enddate>20161012</enddate><creator>Zhou, Junfeng</creator><creator>Wang, Jiajia</creator><creator>Jin, Kaikai</creator><creator>Sun, Jing</creator><creator>Fang, Qiang</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>20161012</creationdate><title>s-Triazine-based functional monomers with thermocrosslinkable propargyl units: Synthesis and conversion to the heat-resistant polymers</title><author>Zhou, Junfeng ; Wang, Jiajia ; Jin, Kaikai ; Sun, Jing ; Fang, Qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-761cb30274fcd5acc73f2af9d379173a5408e6945b71dff7bda19814816b2fdf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Bismaleimides</topic><topic>Blending</topic><topic>Conversion</topic><topic>Crosslinking</topic><topic>Functional polymers</topic><topic>Heat-resistant polymers</topic><topic>Monomers</topic><topic>Propargyl</topic><topic>s-Triazine</topic><topic>Synthesis</topic><topic>Thermal stability</topic><topic>Thermostability</topic><topic>Transportation networks</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Junfeng</creatorcontrib><creatorcontrib>Wang, Jiajia</creatorcontrib><creatorcontrib>Jin, Kaikai</creatorcontrib><creatorcontrib>Sun, Jing</creatorcontrib><creatorcontrib>Fang, Qiang</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology &amp; 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>Zhou, Junfeng</au><au>Wang, Jiajia</au><au>Jin, Kaikai</au><au>Sun, Jing</au><au>Fang, Qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>s-Triazine-based functional monomers with thermocrosslinkable propargyl units: Synthesis and conversion to the heat-resistant polymers</atitle><jtitle>Polymer (Guilford)</jtitle><date>2016-10-12</date><risdate>2016</risdate><volume>102</volume><spage>301</spage><epage>307</epage><pages>301-307</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><abstract>Three s-triazine-based functional monomers with thermo-polymerizable propargyl-ether units were synthesized by a facile procedure. These monomers can be thermally cured to form the crosslinked networks, which showed 5-wt% loss temperature of up to 400 °C and the char yields of more than 50% at 1000 °C. Moreover, the crosslinked networks exhibited the coefficients of thermal expansion (CTE) of below 43 ppm °C−1 varying from 30 to 300 °C and glass transition temperatures (Tg) of up to 290 °C, respectively. These monomers were also used to improve the thermostability of a commercial bismaleimide (4,4′-bismaleimidodiphenylmethane). The results indicated that blending the bismaleimide and the triazine monomers gave the new resins, which showed higher Tg and lower CTE than the bismaleimide, suggesting the triazine monomers can be considered as the modifiers for enhancement of the thermostability of the commercial bismaleimides. s-Triazine-based functional monomers with thermo-polymerizable propargyl-ether units are reported here. Thermopolymerization of the monomers gave the crosslinked networks, showing high low coefficients of thermal expansion (CTE) high glass transition temperatures (Tg). These monomers were also used to improve the properties of a commercial bismaleimide, producing the copolymers with the better thermostability than that the neat bismaleimide. [Display omitted]</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2016.09.027</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0032-3861
ispartof Polymer (Guilford), 2016-10, Vol.102, p.301-307
issn 0032-3861
1873-2291
language eng
recordid cdi_proquest_miscellaneous_1845807865
source Elsevier ScienceDirect Journals
subjects Bismaleimides
Blending
Conversion
Crosslinking
Functional polymers
Heat-resistant polymers
Monomers
Propargyl
s-Triazine
Synthesis
Thermal stability
Thermostability
Transportation networks
title s-Triazine-based functional monomers with thermocrosslinkable propargyl units: Synthesis and conversion to the heat-resistant polymers
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T21%3A19%3A06IST&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=s-Triazine-based%20functional%20monomers%20with%20thermocrosslinkable%20propargyl%20units:%20Synthesis%20and%20conversion%20to%20the%20heat-resistant%20polymers&rft.jtitle=Polymer%20(Guilford)&rft.au=Zhou,%20Junfeng&rft.date=2016-10-12&rft.volume=102&rft.spage=301&rft.epage=307&rft.pages=301-307&rft.issn=0032-3861&rft.eissn=1873-2291&rft_id=info:doi/10.1016/j.polymer.2016.09.027&rft_dat=%3Cproquest_cross%3E1845807865%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=1845807865&rft_id=info:pmid/&rft_els_id=S0032386116308266&rfr_iscdi=true