Fluorescence and IR characterization of epoxy cured with aliphatic amines
Cure reactions of the stoichiometric mixtures of diglycidyl ether of bisphenol A (DGEBA) and two very low molecular weight aliphatic polyether diamines (PED) were studied by using fluorescence and mid- and near-IR spectroscopic techniques. As the cure proceeded, the primary amine groups in PED are c...
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Veröffentlicht in: | Polymer (Guilford) 2005-10, Vol.46 (22), p.9378-9384 |
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description | Cure reactions of the stoichiometric mixtures of diglycidyl ether of bisphenol A (DGEBA) and two very low molecular weight aliphatic polyether diamines (PED) were studied by using fluorescence and mid- and near-IR spectroscopic techniques. As the cure proceeded, the primary amine groups in PED are converted to the secondary and the tertiary amines. Near-IR spectral analysis was used to calculate the concentration of the three amine groups as a function of cure time. The decrease in the fluorescence intensity of DGEBA at about 307
nm was observed due to more effective quenching of the tertiary amine groups in PED, in comparison to the primary and the secondary amine groups. A large decrease in fluorescence intensity at 75 and 95
°C cure was observed. The amount of all the amine species was estimated from NIR spectra to shed light on the cure kinetics of PPO (polypropylene oxide) in comparison with PEO (polyethylene oxide) epoxy, as well as to explain their fluorescence behavior.
The fluorescence intensity changes were correlated to the extent of epoxy reaction obtained by mid- and near-IR spectroscopy. |
doi_str_mv | 10.1016/j.polymer.2005.04.063 |
format | Article |
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nm was observed due to more effective quenching of the tertiary amine groups in PED, in comparison to the primary and the secondary amine groups. A large decrease in fluorescence intensity at 75 and 95
°C cure was observed. The amount of all the amine species was estimated from NIR spectra to shed light on the cure kinetics of PPO (polypropylene oxide) in comparison with PEO (polyethylene oxide) epoxy, as well as to explain their fluorescence behavior.
The fluorescence intensity changes were correlated to the extent of epoxy reaction obtained by mid- and near-IR spectroscopy.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2005.04.063</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Chemical properties ; Diglycidyl ether ; Epoxy resin ; Exact sciences and technology ; Fluorescence spectroscopy ; Polymer industry, paints, wood ; Properties and testing ; Technology of polymers</subject><ispartof>Polymer (Guilford), 2005-10, Vol.46 (22), p.9378-9384</ispartof><rights>2005</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-bd86f41487dc523cd6e0a9bea95374fac76bd86b31efbb8736b3126f0e56ff793</citedby><cites>FETCH-LOGICAL-c401t-bd86f41487dc523cd6e0a9bea95374fac76bd86b31efbb8736b3126f0e56ff793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0032386105005367$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17146917$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Rigail-Cedeño, Andrés</creatorcontrib><creatorcontrib>Sung, Chong Sook Paik</creatorcontrib><title>Fluorescence and IR characterization of epoxy cured with aliphatic amines</title><title>Polymer (Guilford)</title><description>Cure reactions of the stoichiometric mixtures of diglycidyl ether of bisphenol A (DGEBA) and two very low molecular weight aliphatic polyether diamines (PED) were studied by using fluorescence and mid- and near-IR spectroscopic techniques. As the cure proceeded, the primary amine groups in PED are converted to the secondary and the tertiary amines. Near-IR spectral analysis was used to calculate the concentration of the three amine groups as a function of cure time. The decrease in the fluorescence intensity of DGEBA at about 307
nm was observed due to more effective quenching of the tertiary amine groups in PED, in comparison to the primary and the secondary amine groups. A large decrease in fluorescence intensity at 75 and 95
°C cure was observed. The amount of all the amine species was estimated from NIR spectra to shed light on the cure kinetics of PPO (polypropylene oxide) in comparison with PEO (polyethylene oxide) epoxy, as well as to explain their fluorescence behavior.
The fluorescence intensity changes were correlated to the extent of epoxy reaction obtained by mid- and near-IR spectroscopy.</description><subject>Applied sciences</subject><subject>Chemical properties</subject><subject>Diglycidyl ether</subject><subject>Epoxy resin</subject><subject>Exact sciences and technology</subject><subject>Fluorescence spectroscopy</subject><subject>Polymer industry, paints, wood</subject><subject>Properties and testing</subject><subject>Technology of polymers</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkEtr3DAQgEVpoNu0P6GgS3uzM3raPpUSmnQhUCjNWcjyiNXitVzJ23bz6yOzCz02pxmYb14fIR8Y1AyYvtnXcxxPB0w1B1A1yBq0eEU2rG1ExXnHXpMNgOCVaDV7Q97mvAcArrjckO3deIwJs8PJIbXTQLc_qNvZZN2CKTzZJcSJRk9xjn9P1B0TDvRPWHbUjmHelbKj9hAmzO_IlbdjxveXeE0e777-vP1WPXy_395-eaicBLZU_dBqL5lsm8EpLtygEWzXo-2UaKS3rtEr0guGvu_LB2vKtQdU2vumE9fk03nunOKvI-bFHEI5fxzthPGYDW8bqZRuXwAqDp3gBVRn0KWYc0Jv5hQONp0MA7MaNntzMWxWwwakKYZL38fLApudHX2ykwv5X3PDpO5YU7jPZw6Llt-hTMkurL6HkNAtZojhP5ueAWmUlQQ</recordid><startdate>20051024</startdate><enddate>20051024</enddate><creator>Rigail-Cedeño, Andrés</creator><creator>Sung, Chong Sook Paik</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>F28</scope><scope>FR3</scope></search><sort><creationdate>20051024</creationdate><title>Fluorescence and IR characterization of epoxy cured with aliphatic amines</title><author>Rigail-Cedeño, Andrés ; Sung, Chong Sook Paik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-bd86f41487dc523cd6e0a9bea95374fac76bd86b31efbb8736b3126f0e56ff793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Applied sciences</topic><topic>Chemical properties</topic><topic>Diglycidyl ether</topic><topic>Epoxy resin</topic><topic>Exact sciences and technology</topic><topic>Fluorescence spectroscopy</topic><topic>Polymer industry, paints, wood</topic><topic>Properties and testing</topic><topic>Technology of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rigail-Cedeño, Andrés</creatorcontrib><creatorcontrib>Sung, Chong Sook Paik</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rigail-Cedeño, Andrés</au><au>Sung, Chong Sook Paik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorescence and IR characterization of epoxy cured with aliphatic amines</atitle><jtitle>Polymer (Guilford)</jtitle><date>2005-10-24</date><risdate>2005</risdate><volume>46</volume><issue>22</issue><spage>9378</spage><epage>9384</epage><pages>9378-9384</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>Cure reactions of the stoichiometric mixtures of diglycidyl ether of bisphenol A (DGEBA) and two very low molecular weight aliphatic polyether diamines (PED) were studied by using fluorescence and mid- and near-IR spectroscopic techniques. As the cure proceeded, the primary amine groups in PED are converted to the secondary and the tertiary amines. Near-IR spectral analysis was used to calculate the concentration of the three amine groups as a function of cure time. The decrease in the fluorescence intensity of DGEBA at about 307
nm was observed due to more effective quenching of the tertiary amine groups in PED, in comparison to the primary and the secondary amine groups. A large decrease in fluorescence intensity at 75 and 95
°C cure was observed. The amount of all the amine species was estimated from NIR spectra to shed light on the cure kinetics of PPO (polypropylene oxide) in comparison with PEO (polyethylene oxide) epoxy, as well as to explain their fluorescence behavior.
The fluorescence intensity changes were correlated to the extent of epoxy reaction obtained by mid- and near-IR spectroscopy.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2005.04.063</doi><tpages>7</tpages></addata></record> |
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subjects | Applied sciences Chemical properties Diglycidyl ether Epoxy resin Exact sciences and technology Fluorescence spectroscopy Polymer industry, paints, wood Properties and testing Technology of polymers |
title | Fluorescence and IR characterization of epoxy cured with aliphatic amines |
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