Thermal degradation of polyurethane bicomponent systems in controlled atmospheres
Although the thermal degradation of polyurethanes has been extensively studied in the past, the use of a panoply of recent analytical techniques has provided more detailed data and enabled us to confirm prior findings on the thermal degradation of bicomponent polyurethanes. The thermal behaviour of...
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Veröffentlicht in: | Polymers & polymer composites 2005, Vol.13 (1), p.1-26 |
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creator | KETATA, N SANGLAR, C WATON, H ALAMERCERY, S DELOLME, F RAFFIN, G GRENIER-LOUSTALOT, M. F |
description | Although the thermal degradation of polyurethanes has been extensively studied in the past, the use of a panoply of recent analytical techniques has provided more detailed data and enabled us to confirm prior findings on the thermal degradation of bicomponent polyurethanes.
The thermal behaviour of bicomponent polyurethanes in conditions of controlled atmosphere and temperature was characterized by determining their heat stability by on-line TGA/FT-IR coupling and off-line TGA/TCT/GC/MS coupling in order to identify the volatile compounds released. Degradation residues were analyzed by FT-IR and MALDI-TOF (matrix assisted laser desorption/ionization coupled with time-of-flight) mass spectrometry. A major drawback of these thermoplastic elastomers is that one of the components, isocyanate, is toxic.
Based on the data obtained with model urethane compounds ( p-TI-based) and bicomponent polyurethane polymer (MDI- and PEG-based), we show that the thermal degradations are different. The widespread application of these materials exposes them to extreme working conditions, which is why we propose reaction mechanisms for their degradation. |
doi_str_mv | 10.1177/096739110501300101 |
format | Article |
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The thermal behaviour of bicomponent polyurethanes in conditions of controlled atmosphere and temperature was characterized by determining their heat stability by on-line TGA/FT-IR coupling and off-line TGA/TCT/GC/MS coupling in order to identify the volatile compounds released. Degradation residues were analyzed by FT-IR and MALDI-TOF (matrix assisted laser desorption/ionization coupled with time-of-flight) mass spectrometry. A major drawback of these thermoplastic elastomers is that one of the components, isocyanate, is toxic.
Based on the data obtained with model urethane compounds ( p-TI-based) and bicomponent polyurethane polymer (MDI- and PEG-based), we show that the thermal degradations are different. The widespread application of these materials exposes them to extreme working conditions, which is why we propose reaction mechanisms for their degradation.</description><identifier>ISSN: 0967-3911</identifier><identifier>EISSN: 1478-2391</identifier><identifier>DOI: 10.1177/096739110501300101</identifier><language>eng</language><publisher>Shrewsbury: Rapra Technology</publisher><subject>Analytical chemistry ; Applied sciences ; Chemical reactions and properties ; Chemical Sciences ; Degradation ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers</subject><ispartof>Polymers & polymer composites, 2005, Vol.13 (1), p.1-26</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Rapra Technology Limited 2005</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-cab8569f2b46ff78e0fa1671d11ccd40539dd98456b63f51da47f1f9460063023</citedby><cites>FETCH-LOGICAL-c369t-cab8569f2b46ff78e0fa1671d11ccd40539dd98456b63f51da47f1f9460063023</cites><orcidid>0000-0003-0320-0764 ; 0000-0002-7156-2313 ; 0000-0003-4177-2667</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16526617$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00509851$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>KETATA, N</creatorcontrib><creatorcontrib>SANGLAR, C</creatorcontrib><creatorcontrib>WATON, H</creatorcontrib><creatorcontrib>ALAMERCERY, S</creatorcontrib><creatorcontrib>DELOLME, F</creatorcontrib><creatorcontrib>RAFFIN, G</creatorcontrib><creatorcontrib>GRENIER-LOUSTALOT, M. F</creatorcontrib><title>Thermal degradation of polyurethane bicomponent systems in controlled atmospheres</title><title>Polymers & polymer composites</title><description>Although the thermal degradation of polyurethanes has been extensively studied in the past, the use of a panoply of recent analytical techniques has provided more detailed data and enabled us to confirm prior findings on the thermal degradation of bicomponent polyurethanes.
The thermal behaviour of bicomponent polyurethanes in conditions of controlled atmosphere and temperature was characterized by determining their heat stability by on-line TGA/FT-IR coupling and off-line TGA/TCT/GC/MS coupling in order to identify the volatile compounds released. Degradation residues were analyzed by FT-IR and MALDI-TOF (matrix assisted laser desorption/ionization coupled with time-of-flight) mass spectrometry. A major drawback of these thermoplastic elastomers is that one of the components, isocyanate, is toxic.
Based on the data obtained with model urethane compounds ( p-TI-based) and bicomponent polyurethane polymer (MDI- and PEG-based), we show that the thermal degradations are different. The widespread application of these materials exposes them to extreme working conditions, which is why we propose reaction mechanisms for their degradation.</description><subject>Analytical chemistry</subject><subject>Applied sciences</subject><subject>Chemical reactions and properties</subject><subject>Chemical Sciences</subject><subject>Degradation</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><issn>0967-3911</issn><issn>1478-2391</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNplkU9LxDAQxYMouP75Ap6KoOChOtM0SXMUUVdYEEHPIZsmbpe0qUlX2G9vy4qCngYev_eGN0PIGcI1ohA3ILmgEhEYIAVAwD0yw1JUeTHK-2Q2AflEHJKjlNYABXLOZuTldWVjq31W2_eoaz00ocuCy_rgt5toh5XubLZsTGj70NluyNI2DbZNWdNlJnRDDN7bOtNDG1I_Rtl0Qg6c9smefs9j8vZw_3o3zxfPj093t4vcUC6H3Ohlxbh0xbLkzonKgtPIBdaIxtQlMCrrWlYl40tOHcNal8KhkyUH4BQKekyudrkr7VUfm1bHrQq6UfPbhZo0GI8hK4afOLKXO7aP4WNj06DaJhnr_dgubJIqKhSAko3g-R9wHTaxG3solKJkQMWUVuwgE0NK0bqf9Qhqeof6_47RdPGdrJPR3kXdmSb9OjkrOEdBvwC8yojp</recordid><startdate>2005</startdate><enddate>2005</enddate><creator>KETATA, N</creator><creator>SANGLAR, C</creator><creator>WATON, H</creator><creator>ALAMERCERY, S</creator><creator>DELOLME, F</creator><creator>RAFFIN, G</creator><creator>GRENIER-LOUSTALOT, M. 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F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermal degradation of polyurethane bicomponent systems in controlled atmospheres</atitle><jtitle>Polymers & polymer composites</jtitle><date>2005</date><risdate>2005</risdate><volume>13</volume><issue>1</issue><spage>1</spage><epage>26</epage><pages>1-26</pages><issn>0967-3911</issn><eissn>1478-2391</eissn><abstract>Although the thermal degradation of polyurethanes has been extensively studied in the past, the use of a panoply of recent analytical techniques has provided more detailed data and enabled us to confirm prior findings on the thermal degradation of bicomponent polyurethanes.
The thermal behaviour of bicomponent polyurethanes in conditions of controlled atmosphere and temperature was characterized by determining their heat stability by on-line TGA/FT-IR coupling and off-line TGA/TCT/GC/MS coupling in order to identify the volatile compounds released. Degradation residues were analyzed by FT-IR and MALDI-TOF (matrix assisted laser desorption/ionization coupled with time-of-flight) mass spectrometry. A major drawback of these thermoplastic elastomers is that one of the components, isocyanate, is toxic.
Based on the data obtained with model urethane compounds ( p-TI-based) and bicomponent polyurethane polymer (MDI- and PEG-based), we show that the thermal degradations are different. The widespread application of these materials exposes them to extreme working conditions, which is why we propose reaction mechanisms for their degradation.</abstract><cop>Shrewsbury</cop><pub>Rapra Technology</pub><doi>10.1177/096739110501300101</doi><tpages>26</tpages><orcidid>https://orcid.org/0000-0003-0320-0764</orcidid><orcidid>https://orcid.org/0000-0002-7156-2313</orcidid><orcidid>https://orcid.org/0000-0003-4177-2667</orcidid></addata></record> |
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subjects | Analytical chemistry Applied sciences Chemical reactions and properties Chemical Sciences Degradation Exact sciences and technology Organic polymers Physicochemistry of polymers |
title | Thermal degradation of polyurethane bicomponent systems in controlled atmospheres |
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