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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Reactive & functional polymers 2018-08, Vol.129, p.38-45
Hauptverfasser: Roose, Patrice, Herssens, Anita, Lardot, Thierry, Ziegler, Peter, Etz, Oliver, Bontinck, Dirk
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 45
container_issue
container_start_page 38
container_title Reactive & functional polymers
container_volume 129
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2089193179</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1381514817301402</els_id><sourcerecordid>2089193179</sourcerecordid><originalsourceid>FETCH-LOGICAL-c398t-39dafaeb8fae3ef12ad695c6e91f0b1eeda8cb07ca9602dcbec633aeb08864c33</originalsourceid><addsrcrecordid>eNqNUE1LAzEQDaJgrf6HBfG4a2bTZpODBxGtQtGLgreQnZ21WdtNTbZK_fWm1JMnYZgZeB_DPMYugBfAQV52RSCLQ7vpcVj75XZVlByqgqeC8oCNQFUiBylfD9MuFORTmKhjdhJjxxMxISMmHmn48uE9w4UNyYyC-7aD833m22y9oN4vHea1jdRk6BPSv8VTdtTaZaSz3zlmL3e3zzf3-fxp9nBzPc9RaDXkQje2tVSr1AS1UNpG6ilK0tDyGogaq7DmFVotedlgTSiFSAKulJygEGN2vvddB_-xoTiYzm9Cn06akisNWkClE-tqz8LgYwzUmnVwKxu2BrjZ5WQ68ycns8vJ8FRQJv1sr6f0yqejYCI66pEaFwgH03j3T6cfszh9Gg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2089193179</pqid></control><display><type>article</type><title>Network characterization of phenolic-based coatings</title><source>Elsevier ScienceDirect Journals</source><creator>Roose, Patrice ; Herssens, Anita ; Lardot, Thierry ; Ziegler, Peter ; Etz, Oliver ; Bontinck, Dirk</creator><creatorcontrib>Roose, Patrice ; Herssens, Anita ; Lardot, Thierry ; Ziegler, Peter ; Etz, Oliver ; Bontinck, Dirk</creatorcontrib><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><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 &amp; 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 &amp; 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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 1381-5148
ispartof Reactive & functional polymers, 2018-08, Vol.129, p.38-45
issn 1381-5148
1873-166X
language eng
recordid cdi_proquest_journals_2089193179
source Elsevier ScienceDirect Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-22T00%3A52%3A44IST&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=Network%20characterization%20of%20phenolic-based%20coatings&rft.jtitle=Reactive%20&%20functional%20polymers&rft.au=Roose,%20Patrice&rft.date=2018-08-01&rft.volume=129&rft.spage=38&rft.epage=45&rft.pages=38-45&rft.issn=1381-5148&rft.eissn=1873-166X&rft_id=info:doi/10.1016/j.reactfunctpolym.2017.07.012&rft_dat=%3Cproquest_cross%3E2089193179%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=2089193179&rft_id=info:pmid/&rft_els_id=S1381514817301402&rfr_iscdi=true