Network characterization of phenolic-based coatings
Phenolic-based coating systems incorporating typical binding resins such as epoxies or polyesters were prepared along protocols mimicking relevant application conditions and are investigated using methods which are fairly standard in an industrial environment. Following a pragmatic approach, gravime...
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Veröffentlicht in: | Reactive & functional polymers 2018-08, Vol.129, p.38-45 |
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creator | Roose, Patrice Herssens, Anita Lardot, Thierry Ziegler, Peter Etz, Oliver Bontinck, Dirk |
description | Phenolic-based coating systems incorporating typical binding resins such as epoxies or polyesters were prepared along protocols mimicking relevant application conditions and are investigated using methods which are fairly standard in an industrial environment. Following a pragmatic approach, gravimetric analysis along with spectral analysis by FTIR spectroscopy of the insoluble gel fraction and liquid 1H NMR spectroscopy for the soluble fraction were used in a quantitative way to investigate proven binder/crosslinker systems over a range of compositions. Furthermore, a close analysis of the soluble fraction data has been conducted following the statistical mean-field model of Miller-Macosko with proper adjustments to account for the investigated systems where the phenolic resin can crosslink with itself and with the binder, whereas the binder mainly links to the crosslinker in conjunction with chain extending end-end couplings. For the linear precursors considered here, end and side functions were treated as chemically distinct in the model.
The soluble and insoluble fractions of phenolic-based coating systems are characterized by gravimetric and spectral analysis after curing at elevated temperature. The soluble fraction is compared to statistical model predictions obtained following the recursive method of Miller-Macosko. The chemical coupling mechanisms controlling the insoluble gel formation for resole-epoxy and resole-polyester systems are successfully identified. [Display omitted] |
doi_str_mv | 10.1016/j.reactfunctpolym.2017.07.012 |
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The soluble and insoluble fractions of phenolic-based coating systems are characterized by gravimetric and spectral analysis after curing at elevated temperature. The soluble fraction is compared to statistical model predictions obtained following the recursive method of Miller-Macosko. The chemical coupling mechanisms controlling the insoluble gel formation for resole-epoxy and resole-polyester systems are successfully identified. [Display omitted]</description><identifier>ISSN: 1381-5148</identifier><identifier>EISSN: 1873-166X</identifier><identifier>DOI: 10.1016/j.reactfunctpolym.2017.07.012</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Coatings ; Couplings ; Crosslinking ; Epoxy ; Epoxy coatings ; Fourier transforms ; Gravimetric analysis ; Miller-Macosko ; NMR spectroscopy ; Organic chemistry ; Phenolic ; Polyester resins ; Polyesters ; Protocol (computers) ; Resins ; Soluble fraction ; Thermogravimetric analysis</subject><ispartof>Reactive & functional polymers, 2018-08, Vol.129, p.38-45</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright Elsevier BV Aug 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-39dafaeb8fae3ef12ad695c6e91f0b1eeda8cb07ca9602dcbec633aeb08864c33</citedby><cites>FETCH-LOGICAL-c398t-39dafaeb8fae3ef12ad695c6e91f0b1eeda8cb07ca9602dcbec633aeb08864c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1381514817301402$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids></links><search><creatorcontrib>Roose, Patrice</creatorcontrib><creatorcontrib>Herssens, Anita</creatorcontrib><creatorcontrib>Lardot, Thierry</creatorcontrib><creatorcontrib>Ziegler, Peter</creatorcontrib><creatorcontrib>Etz, Oliver</creatorcontrib><creatorcontrib>Bontinck, Dirk</creatorcontrib><title>Network characterization of phenolic-based coatings</title><title>Reactive & functional polymers</title><description>Phenolic-based coating systems incorporating typical binding resins such as epoxies or polyesters were prepared along protocols mimicking relevant application conditions and are investigated using methods which are fairly standard in an industrial environment. Following a pragmatic approach, gravimetric analysis along with spectral analysis by FTIR spectroscopy of the insoluble gel fraction and liquid 1H NMR spectroscopy for the soluble fraction were used in a quantitative way to investigate proven binder/crosslinker systems over a range of compositions. Furthermore, a close analysis of the soluble fraction data has been conducted following the statistical mean-field model of Miller-Macosko with proper adjustments to account for the investigated systems where the phenolic resin can crosslink with itself and with the binder, whereas the binder mainly links to the crosslinker in conjunction with chain extending end-end couplings. For the linear precursors considered here, end and side functions were treated as chemically distinct in the model.
The soluble and insoluble fractions of phenolic-based coating systems are characterized by gravimetric and spectral analysis after curing at elevated temperature. The soluble fraction is compared to statistical model predictions obtained following the recursive method of Miller-Macosko. The chemical coupling mechanisms controlling the insoluble gel formation for resole-epoxy and resole-polyester systems are successfully identified. [Display omitted]</description><subject>Coatings</subject><subject>Couplings</subject><subject>Crosslinking</subject><subject>Epoxy</subject><subject>Epoxy coatings</subject><subject>Fourier transforms</subject><subject>Gravimetric analysis</subject><subject>Miller-Macosko</subject><subject>NMR spectroscopy</subject><subject>Organic chemistry</subject><subject>Phenolic</subject><subject>Polyester resins</subject><subject>Polyesters</subject><subject>Protocol (computers)</subject><subject>Resins</subject><subject>Soluble fraction</subject><subject>Thermogravimetric analysis</subject><issn>1381-5148</issn><issn>1873-166X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqNUE1LAzEQDaJgrf6HBfG4a2bTZpODBxGtQtGLgreQnZ21WdtNTbZK_fWm1JMnYZgZeB_DPMYugBfAQV52RSCLQ7vpcVj75XZVlByqgqeC8oCNQFUiBylfD9MuFORTmKhjdhJjxxMxISMmHmn48uE9w4UNyYyC-7aD833m22y9oN4vHea1jdRk6BPSv8VTdtTaZaSz3zlmL3e3zzf3-fxp9nBzPc9RaDXkQje2tVSr1AS1UNpG6ilK0tDyGogaq7DmFVotedlgTSiFSAKulJygEGN2vvddB_-xoTiYzm9Cn06akisNWkClE-tqz8LgYwzUmnVwKxu2BrjZ5WQ68ycns8vJ8FRQJv1sr6f0yqejYCI66pEaFwgH03j3T6cfszh9Gg</recordid><startdate>20180801</startdate><enddate>20180801</enddate><creator>Roose, Patrice</creator><creator>Herssens, Anita</creator><creator>Lardot, Thierry</creator><creator>Ziegler, Peter</creator><creator>Etz, Oliver</creator><creator>Bontinck, Dirk</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20180801</creationdate><title>Network characterization of phenolic-based coatings</title><author>Roose, Patrice ; Herssens, Anita ; Lardot, Thierry ; Ziegler, Peter ; Etz, Oliver ; Bontinck, Dirk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-39dafaeb8fae3ef12ad695c6e91f0b1eeda8cb07ca9602dcbec633aeb08864c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Coatings</topic><topic>Couplings</topic><topic>Crosslinking</topic><topic>Epoxy</topic><topic>Epoxy coatings</topic><topic>Fourier transforms</topic><topic>Gravimetric analysis</topic><topic>Miller-Macosko</topic><topic>NMR spectroscopy</topic><topic>Organic chemistry</topic><topic>Phenolic</topic><topic>Polyester resins</topic><topic>Polyesters</topic><topic>Protocol (computers)</topic><topic>Resins</topic><topic>Soluble fraction</topic><topic>Thermogravimetric analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roose, Patrice</creatorcontrib><creatorcontrib>Herssens, Anita</creatorcontrib><creatorcontrib>Lardot, Thierry</creatorcontrib><creatorcontrib>Ziegler, Peter</creatorcontrib><creatorcontrib>Etz, Oliver</creatorcontrib><creatorcontrib>Bontinck, Dirk</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Reactive & functional polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roose, Patrice</au><au>Herssens, Anita</au><au>Lardot, Thierry</au><au>Ziegler, Peter</au><au>Etz, Oliver</au><au>Bontinck, Dirk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Network characterization of phenolic-based coatings</atitle><jtitle>Reactive & functional polymers</jtitle><date>2018-08-01</date><risdate>2018</risdate><volume>129</volume><spage>38</spage><epage>45</epage><pages>38-45</pages><issn>1381-5148</issn><eissn>1873-166X</eissn><abstract>Phenolic-based coating systems incorporating typical binding resins such as epoxies or polyesters were prepared along protocols mimicking relevant application conditions and are investigated using methods which are fairly standard in an industrial environment. Following a pragmatic approach, gravimetric analysis along with spectral analysis by FTIR spectroscopy of the insoluble gel fraction and liquid 1H NMR spectroscopy for the soluble fraction were used in a quantitative way to investigate proven binder/crosslinker systems over a range of compositions. Furthermore, a close analysis of the soluble fraction data has been conducted following the statistical mean-field model of Miller-Macosko with proper adjustments to account for the investigated systems where the phenolic resin can crosslink with itself and with the binder, whereas the binder mainly links to the crosslinker in conjunction with chain extending end-end couplings. For the linear precursors considered here, end and side functions were treated as chemically distinct in the model.
The soluble and insoluble fractions of phenolic-based coating systems are characterized by gravimetric and spectral analysis after curing at elevated temperature. The soluble fraction is compared to statistical model predictions obtained following the recursive method of Miller-Macosko. The chemical coupling mechanisms controlling the insoluble gel formation for resole-epoxy and resole-polyester systems are successfully identified. [Display omitted]</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.reactfunctpolym.2017.07.012</doi><tpages>8</tpages></addata></record> |
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subjects | Coatings Couplings Crosslinking Epoxy Epoxy coatings Fourier transforms Gravimetric analysis Miller-Macosko NMR spectroscopy Organic chemistry Phenolic Polyester resins Polyesters Protocol (computers) Resins Soluble fraction Thermogravimetric analysis |
title | Network characterization of phenolic-based coatings |
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