Structure and properties of polyimide films during a far-infrared-induced imidization process

The conversion of poly(amic acid) into polyimide (PI) was achieved with far‐infrared radiation (FIR) and conventional thermal treatments. The structure and properties of PI films during different stages of imidization were studied with Fourier transform infrared spectroscopy, weight‐loss analysis du...

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Veröffentlicht in:Journal of polymer science. Part B, Polymer physics Polymer physics, 2004-07, Vol.42 (13), p.2490-2501
Hauptverfasser: Xu, Yi-Kun, Zhan, Mao-Sheng, Wang, Kai
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container_title Journal of polymer science. Part B, Polymer physics
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creator Xu, Yi-Kun
Zhan, Mao-Sheng
Wang, Kai
description The conversion of poly(amic acid) into polyimide (PI) was achieved with far‐infrared radiation (FIR) and conventional thermal treatments. The structure and properties of PI films during different stages of imidization were studied with Fourier transform infrared spectroscopy, weight‐loss analysis during imidization, tensile property measurements, and dynamic mechanical thermal analysis. The effects of the imidization degree, postimidization, and solvent on the thermal and mechanical properties of PI films were quantitatively investigated. The corresponding structural changes were also examined. The experimental results showed that the imidization process proceeded more quickly and more completely in an FIR oven than in a conventional oven. A prolonged FIR treatment at a lower temperature (25–100 °C) accelerated the imidization process. The tensile stress–strain curves had a fanlike distribution with the development of the FIR imidization process and a fishtail distribution with conventional thermal imidization. During FIR imidization, the best tensile properties were obtained at 340 °C, and thermooxidative degradation occurred at about 420 °C. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 2490–2501, 2004
doi_str_mv 10.1002/polb.20124
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J Polym Sci Part B: Polym Phys 42: 2490–2501, 2004</description><subject>Applied sciences</subject><subject>Chemical modifications</subject><subject>Chemical reactions and properties</subject><subject>Exact sciences and technology</subject><subject>far-infrared radiation (FIR)</subject><subject>imidization degree</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>polyimides</subject><subject>processing</subject><subject>structure-property relations</subject><issn>0887-6266</issn><issn>1099-0488</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp9kE9PwyAYh4nRxDm9-Am46MGkCi2l9KiLTpPFmfjvZAiFF4N27YQ2Oj-9zE29eeIN7_N7CD-E9ik5poSkJ_O2ro5TQlO2gQaUlGVCmBCbaECEKBKecr6NdkJ4ISTu8nKAnm473-uu94BVY_Dct3PwnYOAW4ujbeFmzgC2rp4FbHrvmmessFU-cY31yoOJg-k1GLwk3afqXNssPRpC2EVbVtUB9tbnEN1fnN-NLpPJdHw1Op0kmmWcJaWFKs0pgVKxyprSplUh4kVuNc25AFoxBdYWHHSWl6YoM5NyzbU1urKamWyIDlfe-O5bD6GTMxc01LVqoO2DTAUjhHIewaMVqH0bggcr597NlF9ISuSyQblsUH43GOGDtVUFrer43Ua78JfIBS-YyCJHV9y7q2Hxj1HeTCdnP-5klXGhg4_fjPKvkhdZkcvH67EkD485vcuu5Sj7AkWvkkM</recordid><startdate>20040701</startdate><enddate>20040701</enddate><creator>Xu, Yi-Kun</creator><creator>Zhan, Mao-Sheng</creator><creator>Wang, Kai</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>20040701</creationdate><title>Structure and properties of polyimide films during a far-infrared-induced imidization process</title><author>Xu, Yi-Kun ; Zhan, Mao-Sheng ; Wang, Kai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4364-9feb2510e9a4bfd9f2b782515fc1568e1b4aeff76ec359d793d26c6cfdcbfc4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Applied sciences</topic><topic>Chemical modifications</topic><topic>Chemical reactions and properties</topic><topic>Exact sciences and technology</topic><topic>far-infrared radiation (FIR)</topic><topic>imidization degree</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>polyimides</topic><topic>processing</topic><topic>structure-property relations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Yi-Kun</creatorcontrib><creatorcontrib>Zhan, Mao-Sheng</creatorcontrib><creatorcontrib>Wang, Kai</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 polymer science. 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The structure and properties of PI films during different stages of imidization were studied with Fourier transform infrared spectroscopy, weight‐loss analysis during imidization, tensile property measurements, and dynamic mechanical thermal analysis. The effects of the imidization degree, postimidization, and solvent on the thermal and mechanical properties of PI films were quantitatively investigated. The corresponding structural changes were also examined. The experimental results showed that the imidization process proceeded more quickly and more completely in an FIR oven than in a conventional oven. A prolonged FIR treatment at a lower temperature (25–100 °C) accelerated the imidization process. The tensile stress–strain curves had a fanlike distribution with the development of the FIR imidization process and a fishtail distribution with conventional thermal imidization. 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subjects Applied sciences
Chemical modifications
Chemical reactions and properties
Exact sciences and technology
far-infrared radiation (FIR)
imidization degree
Organic polymers
Physicochemistry of polymers
polyimides
processing
structure-property relations
title Structure and properties of polyimide films during a far-infrared-induced imidization process
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