Polyimides from dianhydrides and bis(p-aminophenyl) alkane diamines. I
Polyimides were synthesized from pyromellitic dianhydride (PMDA), 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride (BTDA), and three different diamines with the following general structure: where R is ethyl, propyl, or isobutyl. The poly(amic acids) obtained had inherent viscosities ranging from 0...
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| Veröffentlicht in: | Journal of polymer science. Polymer chemistry edition 1984-11, Vol.22 (11), p.3359-3365 |
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| container_end_page | 3365 |
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| container_issue | 11 |
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| container_title | Journal of polymer science. Polymer chemistry edition |
| container_volume | 22 |
| creator | Ghatge, N. D. Shinde, B. M. Mulik, U. P. |
| description | Polyimides were synthesized from pyromellitic dianhydride (PMDA), 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride (BTDA), and three different diamines with the following general structure:
where R is ethyl, propyl, or isobutyl. The poly(amic acids) obtained had inherent viscosities ranging from 0.30 to 0.93 and were thermally/chemically converted to polyimides. The thermal stability of the polyimides was evaluated by using dynamic thermogravimetric analysis in air. Physical and thermal properties of these polyimides were compared with that obtained by reacting 2,2‐bis(4‐aminophenyl) propane and PMDA/BTDA. |
| doi_str_mv | 10.1002/pol.1984.170221151 |
| format | Article |
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where R is ethyl, propyl, or isobutyl. The poly(amic acids) obtained had inherent viscosities ranging from 0.30 to 0.93 and were thermally/chemically converted to polyimides. The thermal stability of the polyimides was evaluated by using dynamic thermogravimetric analysis in air. Physical and thermal properties of these polyimides were compared with that obtained by reacting 2,2‐bis(4‐aminophenyl) propane and PMDA/BTDA.</description><identifier>ISSN: 0360-6376</identifier><identifier>EISSN: 1542-9369</identifier><identifier>DOI: 10.1002/pol.1984.170221151</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><ispartof>Journal of polymer science. Polymer chemistry edition, 1984-11, Vol.22 (11), p.3359-3365</ispartof><rights>Copyright © 1984 John Wiley & Sons, Inc.</rights><rights>1985 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3461-b4765aaad69f49dcfc15d2aaf5178e74bcd45a5d8d5515be46ad4edd219726403</citedby><cites>FETCH-LOGICAL-c3461-b4765aaad69f49dcfc15d2aaf5178e74bcd45a5d8d5515be46ad4edd219726403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpol.1984.170221151$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpol.1984.170221151$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9030981$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Ghatge, N. D.</creatorcontrib><creatorcontrib>Shinde, B. M.</creatorcontrib><creatorcontrib>Mulik, U. P.</creatorcontrib><title>Polyimides from dianhydrides and bis(p-aminophenyl) alkane diamines. I</title><title>Journal of polymer science. Polymer chemistry edition</title><addtitle>J. Polym. Sci. Polym. Chem. Ed</addtitle><description>Polyimides were synthesized from pyromellitic dianhydride (PMDA), 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride (BTDA), and three different diamines with the following general structure:
where R is ethyl, propyl, or isobutyl. The poly(amic acids) obtained had inherent viscosities ranging from 0.30 to 0.93 and were thermally/chemically converted to polyimides. The thermal stability of the polyimides was evaluated by using dynamic thermogravimetric analysis in air. Physical and thermal properties of these polyimides were compared with that obtained by reacting 2,2‐bis(4‐aminophenyl) propane and PMDA/BTDA.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><issn>0360-6376</issn><issn>1542-9369</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><recordid>eNqNkEtLw0AUhQdRsFb_gKssXOgicSbzSsCNFFsLwRZ8gZvhJjOhY_NiRtD8exsjxaWrC4fznQsfQucERwTj-Lprq4ikCYuIxHFMCCcHaEI4i8OUivQQTTAVOBRUimN04v07xpRgySZovm6r3tZWGx-Urq0DbaHZ9Nr9JNDoILf-sguhtk3bbUzTV1cBVFtozFDdpcZHwfIUHZVQeXP2e6foeX73NLsPs9ViObvNwoIyQcKcScEBQIu0ZKkuyoJwHQOUnMjESJYXmnHgOtGcE54bJkAzo3VMUhkLhukUxeNu4VrvnSlV52wNrlcEq8GE2plQgwm1N7GDLkaoA19AVTpoCuv3ZIopTpOhdjPWPm1l-n8Mq_Uq-_slHHHrP8zXHge3VUJSydXrw0LJN5qRx5eZovQbgcR_fA</recordid><startdate>198411</startdate><enddate>198411</enddate><creator>Ghatge, N. D.</creator><creator>Shinde, B. M.</creator><creator>Mulik, U. P.</creator><general>John Wiley & Sons, Inc</general><general>Interscience Publishers</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>198411</creationdate><title>Polyimides from dianhydrides and bis(p-aminophenyl) alkane diamines. I</title><author>Ghatge, N. D. ; Shinde, B. M. ; Mulik, U. P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3461-b4765aaad69f49dcfc15d2aaf5178e74bcd45a5d8d5515be46ad4edd219726403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><toplevel>online_resources</toplevel><creatorcontrib>Ghatge, N. D.</creatorcontrib><creatorcontrib>Shinde, B. M.</creatorcontrib><creatorcontrib>Mulik, U. P.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of polymer science. Polymer chemistry edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghatge, N. D.</au><au>Shinde, B. M.</au><au>Mulik, U. P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyimides from dianhydrides and bis(p-aminophenyl) alkane diamines. I</atitle><jtitle>Journal of polymer science. Polymer chemistry edition</jtitle><addtitle>J. Polym. Sci. Polym. Chem. Ed</addtitle><date>1984-11</date><risdate>1984</risdate><volume>22</volume><issue>11</issue><spage>3359</spage><epage>3365</epage><pages>3359-3365</pages><issn>0360-6376</issn><eissn>1542-9369</eissn><abstract>Polyimides were synthesized from pyromellitic dianhydride (PMDA), 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride (BTDA), and three different diamines with the following general structure:
where R is ethyl, propyl, or isobutyl. The poly(amic acids) obtained had inherent viscosities ranging from 0.30 to 0.93 and were thermally/chemically converted to polyimides. The thermal stability of the polyimides was evaluated by using dynamic thermogravimetric analysis in air. Physical and thermal properties of these polyimides were compared with that obtained by reacting 2,2‐bis(4‐aminophenyl) propane and PMDA/BTDA.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/pol.1984.170221151</doi><tpages>7</tpages></addata></record> |
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| issn | 0360-6376 1542-9369 |
| language | eng |
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| source | Wiley Journals |
| subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Polymers with particular properties Preparation, kinetics, thermodynamics, mechanism and catalysts |
| title | Polyimides from dianhydrides and bis(p-aminophenyl) alkane diamines. I |
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