Loading…

Bismaleimide resin modified with diallyl bisphenol A and diallyl p-phenyl diamine for resin transfer molding

O,O′‐diallyl bisphenol A (DBA) and N,N′‐diallyl p‐phenyl diamine (DPD) were used for the reactive diluents of 4,4′‐bismaleimidodiphenol methane (BDM). The objective was to obtain a modified BDM resin system suitable for resin transfer molding (RTM) process to prepare the advanced composites. The pro...

Full description

Saved in:
Bibliographic Details
Published in:Journal of applied polymer science 2001-06, Vol.80 (12), p.2245-2250
Main Authors: Li, Zhongming, Yang, Mingbo, Huang, Rui, Zhang, Meidong, Feng, Jianmin
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3608-5edd2af9671a38577c0d90a1a2de750ef96ff9d05a255190c0747214eff633903
cites cdi_FETCH-LOGICAL-c3608-5edd2af9671a38577c0d90a1a2de750ef96ff9d05a255190c0747214eff633903
container_end_page 2250
container_issue 12
container_start_page 2245
container_title Journal of applied polymer science
container_volume 80
creator Li, Zhongming
Yang, Mingbo
Huang, Rui
Zhang, Meidong
Feng, Jianmin
description O,O′‐diallyl bisphenol A (DBA) and N,N′‐diallyl p‐phenyl diamine (DPD) were used for the reactive diluents of 4,4′‐bismaleimidodiphenol methane (BDM). The objective was to obtain a modified BDM resin system suitable for resin transfer molding (RTM) process to prepare the advanced composites. The processing behavior was determined by time–temperature–viscosity curves, gel characteristics, and differential scanning calorimetry (DSC). The injection temperature of the resin system in RTM could be 80°C, at which its apparent viscosity was only 0.31 Pa/s, and the apparent viscosity was still less than 1.00 Pa/s after the resin was held at 80°C for 16 h. The gel time test result indicated that at low temperatures, the reactivity of the resin system is low, whereas at high temperatures, the resin could cure very fast, which was beneficial to RTM. The postcure of the cured resin at a given temperature was necessary because the resin had a wide and flat cure exothermic peak, observed by DSC curve. The cured resin displayed both high heat and hot/wet resistance and high mechanical properties, especially tensile strength, tensile modulus, and flexural strength at room temperature, which reached 96.2 MPa, 4.8 GPa, and 121.4 MPa, respectively. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 2245–2250, 2001
doi_str_mv 10.1002/app.1328
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_26634974</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>26634974</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3608-5edd2af9671a38577c0d90a1a2de750ef96ff9d05a255190c0747214eff633903</originalsourceid><addsrcrecordid>eNp1kE1rGzEQhkVoIG5SyE9YCIRe1hlJq9Xq6JrGDYQ2h6SGXIS6GtVKtB-VHFL_-8p48a2nGd55eGBeQi4pzCkAuzHjOKecNSdkRkHJsqpZ84HM8omWjVLijHxM6QWAUgH1jIQvPnUmoO-8xSJi8n3RDdY7j7Z499tNYb0JYReKXz6NG-yHUCwK09tjPpb7OC856HyPhRviJNpG0yeHMRuD9f3vC3LqTEj4aZrn5On26-PyW3n_Y3W3XNyXLa-hKQVay4xTtaSGN0LKFqwCQw2zKAVgvjinLAjDhKAKWpCVZLRC52rOFfBzcn3wjnH484ZpqzufWgzB9Di8Jc3qmldKVhn8fADbOKQU0ekx-s7Enaag93XqXKfe15nRq8lpUmuCy6-1Ph35bGNKZqo8UO8-4O6_Nr14eJisE-_TFv8eeRNfdS25FHr9faV_rlfwfMuFbvg_56aSvA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>26634974</pqid></control><display><type>article</type><title>Bismaleimide resin modified with diallyl bisphenol A and diallyl p-phenyl diamine for resin transfer molding</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Li, Zhongming ; Yang, Mingbo ; Huang, Rui ; Zhang, Meidong ; Feng, Jianmin</creator><creatorcontrib>Li, Zhongming ; Yang, Mingbo ; Huang, Rui ; Zhang, Meidong ; Feng, Jianmin</creatorcontrib><description>O,O′‐diallyl bisphenol A (DBA) and N,N′‐diallyl p‐phenyl diamine (DPD) were used for the reactive diluents of 4,4′‐bismaleimidodiphenol methane (BDM). The objective was to obtain a modified BDM resin system suitable for resin transfer molding (RTM) process to prepare the advanced composites. The processing behavior was determined by time–temperature–viscosity curves, gel characteristics, and differential scanning calorimetry (DSC). The injection temperature of the resin system in RTM could be 80°C, at which its apparent viscosity was only 0.31 Pa/s, and the apparent viscosity was still less than 1.00 Pa/s after the resin was held at 80°C for 16 h. The gel time test result indicated that at low temperatures, the reactivity of the resin system is low, whereas at high temperatures, the resin could cure very fast, which was beneficial to RTM. The postcure of the cured resin at a given temperature was necessary because the resin had a wide and flat cure exothermic peak, observed by DSC curve. The cured resin displayed both high heat and hot/wet resistance and high mechanical properties, especially tensile strength, tensile modulus, and flexural strength at room temperature, which reached 96.2 MPa, 4.8 GPa, and 121.4 MPa, respectively. © 2001 John Wiley &amp; Sons, Inc. J Appl Polym Sci 80: 2245–2250, 2001</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.1328</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>Applied sciences ; bismaleimidodiphenol methane ; Chemical properties ; diallyl bisphenol A ; diallyl p-phenyl diamine ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Polycondensation ; Polymer industry, paints, wood ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Properties and testing ; reactive diluents ; resin transfer molding ; Technology of polymers</subject><ispartof>Journal of applied polymer science, 2001-06, Vol.80 (12), p.2245-2250</ispartof><rights>Copyright © 2001 John Wiley &amp; Sons, Inc.</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3608-5edd2af9671a38577c0d90a1a2de750ef96ff9d05a255190c0747214eff633903</citedby><cites>FETCH-LOGICAL-c3608-5edd2af9671a38577c0d90a1a2de750ef96ff9d05a255190c0747214eff633903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=974297$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Zhongming</creatorcontrib><creatorcontrib>Yang, Mingbo</creatorcontrib><creatorcontrib>Huang, Rui</creatorcontrib><creatorcontrib>Zhang, Meidong</creatorcontrib><creatorcontrib>Feng, Jianmin</creatorcontrib><title>Bismaleimide resin modified with diallyl bisphenol A and diallyl p-phenyl diamine for resin transfer molding</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>O,O′‐diallyl bisphenol A (DBA) and N,N′‐diallyl p‐phenyl diamine (DPD) were used for the reactive diluents of 4,4′‐bismaleimidodiphenol methane (BDM). The objective was to obtain a modified BDM resin system suitable for resin transfer molding (RTM) process to prepare the advanced composites. The processing behavior was determined by time–temperature–viscosity curves, gel characteristics, and differential scanning calorimetry (DSC). The injection temperature of the resin system in RTM could be 80°C, at which its apparent viscosity was only 0.31 Pa/s, and the apparent viscosity was still less than 1.00 Pa/s after the resin was held at 80°C for 16 h. The gel time test result indicated that at low temperatures, the reactivity of the resin system is low, whereas at high temperatures, the resin could cure very fast, which was beneficial to RTM. The postcure of the cured resin at a given temperature was necessary because the resin had a wide and flat cure exothermic peak, observed by DSC curve. The cured resin displayed both high heat and hot/wet resistance and high mechanical properties, especially tensile strength, tensile modulus, and flexural strength at room temperature, which reached 96.2 MPa, 4.8 GPa, and 121.4 MPa, respectively. © 2001 John Wiley &amp; Sons, Inc. J Appl Polym Sci 80: 2245–2250, 2001</description><subject>Applied sciences</subject><subject>bismaleimidodiphenol methane</subject><subject>Chemical properties</subject><subject>diallyl bisphenol A</subject><subject>diallyl p-phenyl diamine</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polycondensation</subject><subject>Polymer industry, paints, wood</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Properties and testing</subject><subject>reactive diluents</subject><subject>resin transfer molding</subject><subject>Technology of polymers</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kE1rGzEQhkVoIG5SyE9YCIRe1hlJq9Xq6JrGDYQ2h6SGXIS6GtVKtB-VHFL_-8p48a2nGd55eGBeQi4pzCkAuzHjOKecNSdkRkHJsqpZ84HM8omWjVLijHxM6QWAUgH1jIQvPnUmoO-8xSJi8n3RDdY7j7Z499tNYb0JYReKXz6NG-yHUCwK09tjPpb7OC856HyPhRviJNpG0yeHMRuD9f3vC3LqTEj4aZrn5On26-PyW3n_Y3W3XNyXLa-hKQVay4xTtaSGN0LKFqwCQw2zKAVgvjinLAjDhKAKWpCVZLRC52rOFfBzcn3wjnH484ZpqzufWgzB9Di8Jc3qmldKVhn8fADbOKQU0ekx-s7Enaag93XqXKfe15nRq8lpUmuCy6-1Ph35bGNKZqo8UO8-4O6_Nr14eJisE-_TFv8eeRNfdS25FHr9faV_rlfwfMuFbvg_56aSvA</recordid><startdate>20010620</startdate><enddate>20010620</enddate><creator>Li, Zhongming</creator><creator>Yang, Mingbo</creator><creator>Huang, Rui</creator><creator>Zhang, Meidong</creator><creator>Feng, Jianmin</creator><general>John Wiley &amp; 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>20010620</creationdate><title>Bismaleimide resin modified with diallyl bisphenol A and diallyl p-phenyl diamine for resin transfer molding</title><author>Li, Zhongming ; Yang, Mingbo ; Huang, Rui ; Zhang, Meidong ; Feng, Jianmin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3608-5edd2af9671a38577c0d90a1a2de750ef96ff9d05a255190c0747214eff633903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Applied sciences</topic><topic>bismaleimidodiphenol methane</topic><topic>Chemical properties</topic><topic>diallyl bisphenol A</topic><topic>diallyl p-phenyl diamine</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polycondensation</topic><topic>Polymer industry, paints, wood</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Properties and testing</topic><topic>reactive diluents</topic><topic>resin transfer molding</topic><topic>Technology of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Zhongming</creatorcontrib><creatorcontrib>Yang, Mingbo</creatorcontrib><creatorcontrib>Huang, Rui</creatorcontrib><creatorcontrib>Zhang, Meidong</creatorcontrib><creatorcontrib>Feng, Jianmin</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>Li, Zhongming</au><au>Yang, Mingbo</au><au>Huang, Rui</au><au>Zhang, Meidong</au><au>Feng, Jianmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bismaleimide resin modified with diallyl bisphenol A and diallyl p-phenyl diamine for resin transfer molding</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2001-06-20</date><risdate>2001</risdate><volume>80</volume><issue>12</issue><spage>2245</spage><epage>2250</epage><pages>2245-2250</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>O,O′‐diallyl bisphenol A (DBA) and N,N′‐diallyl p‐phenyl diamine (DPD) were used for the reactive diluents of 4,4′‐bismaleimidodiphenol methane (BDM). The objective was to obtain a modified BDM resin system suitable for resin transfer molding (RTM) process to prepare the advanced composites. The processing behavior was determined by time–temperature–viscosity curves, gel characteristics, and differential scanning calorimetry (DSC). The injection temperature of the resin system in RTM could be 80°C, at which its apparent viscosity was only 0.31 Pa/s, and the apparent viscosity was still less than 1.00 Pa/s after the resin was held at 80°C for 16 h. The gel time test result indicated that at low temperatures, the reactivity of the resin system is low, whereas at high temperatures, the resin could cure very fast, which was beneficial to RTM. The postcure of the cured resin at a given temperature was necessary because the resin had a wide and flat cure exothermic peak, observed by DSC curve. The cured resin displayed both high heat and hot/wet resistance and high mechanical properties, especially tensile strength, tensile modulus, and flexural strength at room temperature, which reached 96.2 MPa, 4.8 GPa, and 121.4 MPa, respectively. © 2001 John Wiley &amp; Sons, Inc. J Appl Polym Sci 80: 2245–2250, 2001</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1002/app.1328</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-8995
ispartof Journal of applied polymer science, 2001-06, Vol.80 (12), p.2245-2250
issn 0021-8995
1097-4628
language eng
recordid cdi_proquest_miscellaneous_26634974
source Wiley-Blackwell Read & Publish Collection
subjects Applied sciences
bismaleimidodiphenol methane
Chemical properties
diallyl bisphenol A
diallyl p-phenyl diamine
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
Polycondensation
Polymer industry, paints, wood
Preparation, kinetics, thermodynamics, mechanism and catalysts
Properties and testing
reactive diluents
resin transfer molding
Technology of polymers
title Bismaleimide resin modified with diallyl bisphenol A and diallyl p-phenyl diamine for resin transfer molding
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T13%3A02%3A31IST&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=Bismaleimide%20resin%20modified%20with%20diallyl%20bisphenol%20A%20and%20diallyl%20p-phenyl%20diamine%20for%20resin%20transfer%20molding&rft.jtitle=Journal%20of%20applied%20polymer%20science&rft.au=Li,%20Zhongming&rft.date=2001-06-20&rft.volume=80&rft.issue=12&rft.spage=2245&rft.epage=2250&rft.pages=2245-2250&rft.issn=0021-8995&rft.eissn=1097-4628&rft.coden=JAPNAB&rft_id=info:doi/10.1002/app.1328&rft_dat=%3Cproquest_cross%3E26634974%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3608-5edd2af9671a38577c0d90a1a2de750ef96ff9d05a255190c0747214eff633903%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=26634974&rft_id=info:pmid/&rfr_iscdi=true