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Structure and Properties of Novel Asymmetric Biphenyl Type Polyimides. Homo- and Copolymers and Blends
Asymmetric biphenyl type polyimides (PI) were prepared by thermal imidization of polyamic acids (PAA) derived from 2,3,3‘,4‘-biphenyltetracarboxylic dianhydride (a-BPDA) and p-phenylenediamine (PDA) or 4,4‘-oxydianiline (ODA). The dynamic mechanical properties of these PIs were compared with those o...
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Published in: | Macromolecules 1999-01, Vol.32 (2), p.387-396 |
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creator | Hasegawa, Masatoshi Sensui, Nobuyuki Shindo, Yoichi Yokota, Rikio |
description | Asymmetric biphenyl type polyimides (PI) were prepared by thermal imidization of polyamic acids (PAA) derived from 2,3,3‘,4‘-biphenyltetracarboxylic dianhydride (a-BPDA) and p-phenylenediamine (PDA) or 4,4‘-oxydianiline (ODA). The dynamic mechanical properties of these PIs were compared with those of the isomeric PIs derived from symmetric 3,4,3‘,4‘-biphenyltetracarboxylic dianhydride (s-BPDA). a-BPDA/PDA polyimide has a considerably bent chain structure compared to semirigid s-BPDA/PDA. Nevertheless, the a-BPDA/PDA film annealed at 350 °C showed a higher T g than the s-BPDA/PDA film prepared under the same conditions. When these PIs were annealed at 400 °C, a-BPDA/PDA exhibited an abrupt E‘ decrease at the T g (=410 °C) as well as the counterpart annealed at 350 °C, whereas s-BPDA/PDA showed no distinct T g in the E‘ curve. Similar annealing effects were also observed for the ODA systems. The unexpectedly higher T g's of a-BPDA-based PIs could be explained in terms of the more restricted conformational change through the crank shaft-like motion. The difference between the extents of the E‘ decrease at the T g for a- and s-BPDA-based PIs is attributed to the difference of the intensity of intermolecular interactions. The blends of s-BPDA/PDA with a-BPDA-based PI (80/20) and the corresponding copolyimide improved the insufficient thermal processability of homo s-BPDA/PDA without causing a decrease in T g. The results revealed that, for semirigid s-BPDA/PDA, a-BPDA-based PIs are better matrix polymers than s-BPDA/ODA. |
doi_str_mv | 10.1021/ma9808629 |
format | article |
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Nevertheless, the a-BPDA/PDA film annealed at 350 °C showed a higher T g than the s-BPDA/PDA film prepared under the same conditions. When these PIs were annealed at 400 °C, a-BPDA/PDA exhibited an abrupt E‘ decrease at the T g (=410 °C) as well as the counterpart annealed at 350 °C, whereas s-BPDA/PDA showed no distinct T g in the E‘ curve. Similar annealing effects were also observed for the ODA systems. The unexpectedly higher T g's of a-BPDA-based PIs could be explained in terms of the more restricted conformational change through the crank shaft-like motion. The difference between the extents of the E‘ decrease at the T g for a- and s-BPDA-based PIs is attributed to the difference of the intensity of intermolecular interactions. The blends of s-BPDA/PDA with a-BPDA-based PI (80/20) and the corresponding copolyimide improved the insufficient thermal processability of homo s-BPDA/PDA without causing a decrease in T g. The results revealed that, for semirigid s-BPDA/PDA, a-BPDA-based PIs are better matrix polymers than s-BPDA/ODA.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma9808629</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Properties and characterization ; Rheology and viscoelasticity</subject><ispartof>Macromolecules, 1999-01, Vol.32 (2), p.387-396</ispartof><rights>Copyright © 1999 American Chemical Society</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a390t-6c4183b649cf88b1c24955f8e2b8482749b8dde1d3f6ad774df5bac2a6bf72543</citedby><cites>FETCH-LOGICAL-a390t-6c4183b649cf88b1c24955f8e2b8482749b8dde1d3f6ad774df5bac2a6bf72543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1666251$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Hasegawa, Masatoshi</creatorcontrib><creatorcontrib>Sensui, Nobuyuki</creatorcontrib><creatorcontrib>Shindo, Yoichi</creatorcontrib><creatorcontrib>Yokota, Rikio</creatorcontrib><title>Structure and Properties of Novel Asymmetric Biphenyl Type Polyimides. Homo- and Copolymers and Blends</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Asymmetric biphenyl type polyimides (PI) were prepared by thermal imidization of polyamic acids (PAA) derived from 2,3,3‘,4‘-biphenyltetracarboxylic dianhydride (a-BPDA) and p-phenylenediamine (PDA) or 4,4‘-oxydianiline (ODA). The dynamic mechanical properties of these PIs were compared with those of the isomeric PIs derived from symmetric 3,4,3‘,4‘-biphenyltetracarboxylic dianhydride (s-BPDA). a-BPDA/PDA polyimide has a considerably bent chain structure compared to semirigid s-BPDA/PDA. Nevertheless, the a-BPDA/PDA film annealed at 350 °C showed a higher T g than the s-BPDA/PDA film prepared under the same conditions. When these PIs were annealed at 400 °C, a-BPDA/PDA exhibited an abrupt E‘ decrease at the T g (=410 °C) as well as the counterpart annealed at 350 °C, whereas s-BPDA/PDA showed no distinct T g in the E‘ curve. Similar annealing effects were also observed for the ODA systems. The unexpectedly higher T g's of a-BPDA-based PIs could be explained in terms of the more restricted conformational change through the crank shaft-like motion. The difference between the extents of the E‘ decrease at the T g for a- and s-BPDA-based PIs is attributed to the difference of the intensity of intermolecular interactions. The blends of s-BPDA/PDA with a-BPDA-based PI (80/20) and the corresponding copolyimide improved the insufficient thermal processability of homo s-BPDA/PDA without causing a decrease in T g. The results revealed that, for semirigid s-BPDA/PDA, a-BPDA-based PIs are better matrix polymers than s-BPDA/ODA.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Rheology and viscoelasticity</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNptkDFPwzAQhS0EEqUw8A88wMCQYjuxY49tgRYJQUULq-U4tkhJ4shOEfn3pC0qC9Pp7r57p_cAuMRohBHBt5USHHFGxBEYYEpQRHlMj8EAIZJEgoj0FJyFsEYIY5rEA2CXrd_oduMNVHUOF941xreFCdBZ-Oy-TAnHoasq0_pCw0nRfJi6K-GqawxcuLIrqiI3YQTnrnLRTmLqmn5eGR927aQ0dR7OwYlVZTAXv3UI3h7uV9N59PQye5yOnyIVC9RGTCeYxxlLhLacZ1iTRFBquSEZTzhJE5HxPDc4jy1TeZomuaWZ0kSxzKakNzQEN3td7V0I3ljZ-KJSvpMYyW1A8hBQz17t2UYFrUrrVa2L8HfAGCMU91i0x4rQmu_DWvlPydI4pXK1WMq7V5K-88lMbmWv97zSQa7dxte94X_e_wAj0YCp</recordid><startdate>19990126</startdate><enddate>19990126</enddate><creator>Hasegawa, Masatoshi</creator><creator>Sensui, Nobuyuki</creator><creator>Shindo, Yoichi</creator><creator>Yokota, Rikio</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990126</creationdate><title>Structure and Properties of Novel Asymmetric Biphenyl Type Polyimides. Homo- and Copolymers and Blends</title><author>Hasegawa, Masatoshi ; Sensui, Nobuyuki ; Shindo, Yoichi ; Yokota, Rikio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a390t-6c4183b649cf88b1c24955f8e2b8482749b8dde1d3f6ad774df5bac2a6bf72543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>Rheology and viscoelasticity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hasegawa, Masatoshi</creatorcontrib><creatorcontrib>Sensui, Nobuyuki</creatorcontrib><creatorcontrib>Shindo, Yoichi</creatorcontrib><creatorcontrib>Yokota, Rikio</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hasegawa, Masatoshi</au><au>Sensui, Nobuyuki</au><au>Shindo, Yoichi</au><au>Yokota, Rikio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure and Properties of Novel Asymmetric Biphenyl Type Polyimides. Homo- and Copolymers and Blends</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>1999-01-26</date><risdate>1999</risdate><volume>32</volume><issue>2</issue><spage>387</spage><epage>396</epage><pages>387-396</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Asymmetric biphenyl type polyimides (PI) were prepared by thermal imidization of polyamic acids (PAA) derived from 2,3,3‘,4‘-biphenyltetracarboxylic dianhydride (a-BPDA) and p-phenylenediamine (PDA) or 4,4‘-oxydianiline (ODA). The dynamic mechanical properties of these PIs were compared with those of the isomeric PIs derived from symmetric 3,4,3‘,4‘-biphenyltetracarboxylic dianhydride (s-BPDA). a-BPDA/PDA polyimide has a considerably bent chain structure compared to semirigid s-BPDA/PDA. Nevertheless, the a-BPDA/PDA film annealed at 350 °C showed a higher T g than the s-BPDA/PDA film prepared under the same conditions. When these PIs were annealed at 400 °C, a-BPDA/PDA exhibited an abrupt E‘ decrease at the T g (=410 °C) as well as the counterpart annealed at 350 °C, whereas s-BPDA/PDA showed no distinct T g in the E‘ curve. Similar annealing effects were also observed for the ODA systems. The unexpectedly higher T g's of a-BPDA-based PIs could be explained in terms of the more restricted conformational change through the crank shaft-like motion. The difference between the extents of the E‘ decrease at the T g for a- and s-BPDA-based PIs is attributed to the difference of the intensity of intermolecular interactions. The blends of s-BPDA/PDA with a-BPDA-based PI (80/20) and the corresponding copolyimide improved the insufficient thermal processability of homo s-BPDA/PDA without causing a decrease in T g. The results revealed that, for semirigid s-BPDA/PDA, a-BPDA-based PIs are better matrix polymers than s-BPDA/ODA.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma9808629</doi><tpages>10</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Properties and characterization Rheology and viscoelasticity |
title | Structure and Properties of Novel Asymmetric Biphenyl Type Polyimides. Homo- and Copolymers and Blends |
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