Dielectric Properties of Bisphenol A Polycarbonate and Its Tethered Nitrile Analogue
The relative permittivity and dielectric strength have been determined for a bisphenol A polycarbonate (BPA-PC), in which a cyanoethyl group has been substituted for one of the geminal dimethyl groups. The new material (CN-PC) has a glass transition temperature that is 19 K higher than that for BPA-...
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Veröffentlicht in: | Macromolecules 2013-05, Vol.46 (10), p.4024-4033 |
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creator | Bendler, John T Boyles, David A Edmondson, Charles A Filipova, Tsvetanka Fontanella, John J Westgate, Mark A Wintersgill, M. C |
description | The relative permittivity and dielectric strength have been determined for a bisphenol A polycarbonate (BPA-PC), in which a cyanoethyl group has been substituted for one of the geminal dimethyl groups. The new material (CN-PC) has a glass transition temperature that is 19 K higher than that for BPA-PC. In addition, the dielectric strength of CN-PC, 405 V/μm, is somewhat smaller than that for BPA-PC, 620 V/μm. The relative permittivity was determined from 10 to 105 Hz over a wide temperature range and at pressures up to 0.25 GPa. While the real part of the relative permittivity at 103 Hz and room temperature for BPA-PC is about 3, that for CN-PC is found to be greater than 4. Correspondingly, the γ relaxation region in CN-PC is very strong. For the γ relaxation, a strong increase in peak height as temperature increases and a strong decrease in peak height as pressure increases are observed. A relaxation is found at temperatures higher than the γ relaxation. This process is labeled as the β relaxation because it appears to be related to the β relaxation in BPA-PC in that the strength and position depend on the history of the material. The effects of pressure on the γ relaxation for both CN-PC and BPA-PC are quite large and similar to those previously seen for the γ relaxation in a fluorinated tetraaryl bisphenol A polycarbonate (DiF p-TABPA-PC). In fact, the activation volume is found to be approximately the same for all three BPA-PC-based materials despite wide variations in both peak position and peak height. Finally, computer studies of the model compounds, 4,4′-diphenylpentanenitrile and diphenyl carbonate, were carried out. Both provide insight into the nature of the γ relaxation with the latter yielding an activation volume in approximate agreement with the experimental values. |
doi_str_mv | 10.1021/ma4002269 |
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C</creator><creatorcontrib>Bendler, John T ; Boyles, David A ; Edmondson, Charles A ; Filipova, Tsvetanka ; Fontanella, John J ; Westgate, Mark A ; Wintersgill, M. C</creatorcontrib><description>The relative permittivity and dielectric strength have been determined for a bisphenol A polycarbonate (BPA-PC), in which a cyanoethyl group has been substituted for one of the geminal dimethyl groups. The new material (CN-PC) has a glass transition temperature that is 19 K higher than that for BPA-PC. In addition, the dielectric strength of CN-PC, 405 V/μm, is somewhat smaller than that for BPA-PC, 620 V/μm. The relative permittivity was determined from 10 to 105 Hz over a wide temperature range and at pressures up to 0.25 GPa. While the real part of the relative permittivity at 103 Hz and room temperature for BPA-PC is about 3, that for CN-PC is found to be greater than 4. Correspondingly, the γ relaxation region in CN-PC is very strong. For the γ relaxation, a strong increase in peak height as temperature increases and a strong decrease in peak height as pressure increases are observed. A relaxation is found at temperatures higher than the γ relaxation. This process is labeled as the β relaxation because it appears to be related to the β relaxation in BPA-PC in that the strength and position depend on the history of the material. The effects of pressure on the γ relaxation for both CN-PC and BPA-PC are quite large and similar to those previously seen for the γ relaxation in a fluorinated tetraaryl bisphenol A polycarbonate (DiF p-TABPA-PC). In fact, the activation volume is found to be approximately the same for all three BPA-PC-based materials despite wide variations in both peak position and peak height. Finally, computer studies of the model compounds, 4,4′-diphenylpentanenitrile and diphenyl carbonate, were carried out. Both provide insight into the nature of the γ relaxation with the latter yielding an activation volume in approximate agreement with the experimental values.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma4002269</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Electrical, magnetic and optical properties ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Properties and characterization</subject><ispartof>Macromolecules, 2013-05, Vol.46 (10), p.4024-4033</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a289t-a916baba3560d39672308d2bbde021196c6c9ad8cc42751499b89f8daff365933</citedby><cites>FETCH-LOGICAL-a289t-a916baba3560d39672308d2bbde021196c6c9ad8cc42751499b89f8daff365933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma4002269$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma4002269$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27481006$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Bendler, John T</creatorcontrib><creatorcontrib>Boyles, David A</creatorcontrib><creatorcontrib>Edmondson, Charles A</creatorcontrib><creatorcontrib>Filipova, Tsvetanka</creatorcontrib><creatorcontrib>Fontanella, John J</creatorcontrib><creatorcontrib>Westgate, Mark A</creatorcontrib><creatorcontrib>Wintersgill, M. C</creatorcontrib><title>Dielectric Properties of Bisphenol A Polycarbonate and Its Tethered Nitrile Analogue</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>The relative permittivity and dielectric strength have been determined for a bisphenol A polycarbonate (BPA-PC), in which a cyanoethyl group has been substituted for one of the geminal dimethyl groups. The new material (CN-PC) has a glass transition temperature that is 19 K higher than that for BPA-PC. In addition, the dielectric strength of CN-PC, 405 V/μm, is somewhat smaller than that for BPA-PC, 620 V/μm. The relative permittivity was determined from 10 to 105 Hz over a wide temperature range and at pressures up to 0.25 GPa. While the real part of the relative permittivity at 103 Hz and room temperature for BPA-PC is about 3, that for CN-PC is found to be greater than 4. Correspondingly, the γ relaxation region in CN-PC is very strong. For the γ relaxation, a strong increase in peak height as temperature increases and a strong decrease in peak height as pressure increases are observed. A relaxation is found at temperatures higher than the γ relaxation. This process is labeled as the β relaxation because it appears to be related to the β relaxation in BPA-PC in that the strength and position depend on the history of the material. The effects of pressure on the γ relaxation for both CN-PC and BPA-PC are quite large and similar to those previously seen for the γ relaxation in a fluorinated tetraaryl bisphenol A polycarbonate (DiF p-TABPA-PC). In fact, the activation volume is found to be approximately the same for all three BPA-PC-based materials despite wide variations in both peak position and peak height. Finally, computer studies of the model compounds, 4,4′-diphenylpentanenitrile and diphenyl carbonate, were carried out. Both provide insight into the nature of the γ relaxation with the latter yielding an activation volume in approximate agreement with the experimental values.</description><subject>Applied sciences</subject><subject>Electrical, magnetic and optical properties</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNptkDtPwzAcxC0EEqUw8A28MDAE_IgdeyzlVamCDmWO_vGDpnLjyE4Hvj1BRWVhOun0u5PuELqm5I4SRu93UBLCmNQnaEIFI4VQXJyiyWiWhWa6OkcXOW8JoVSUfILWj60LzgypNXiVYu_S0LqMo8cPbe43rosBz_Aqhi8DqYkdDA5DZ_FiyHjtho1LzuK3dswHh2cdhPi5d5fozEPI7upXp-jj-Wk9fy2W7y-L-WxZAFN6KEBT2UADXEhiuZYV40RZ1jTWjVOolkYaDVYZU7JK0FLrRmmvLHjPpdCcT9HtodekmHNyvu5Tu4P0VVNS_9xRH-8Y2ZsD20M2EHyCzrT5GGBVqSgh8o8Dk-tt3KdxU_6n7xshpGqb</recordid><startdate>20130528</startdate><enddate>20130528</enddate><creator>Bendler, John T</creator><creator>Boyles, David A</creator><creator>Edmondson, Charles A</creator><creator>Filipova, Tsvetanka</creator><creator>Fontanella, John J</creator><creator>Westgate, Mark A</creator><creator>Wintersgill, M. C</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20130528</creationdate><title>Dielectric Properties of Bisphenol A Polycarbonate and Its Tethered Nitrile Analogue</title><author>Bendler, John T ; Boyles, David A ; Edmondson, Charles A ; Filipova, Tsvetanka ; Fontanella, John J ; Westgate, Mark A ; Wintersgill, M. C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a289t-a916baba3560d39672308d2bbde021196c6c9ad8cc42751499b89f8daff365933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Applied sciences</topic><topic>Electrical, magnetic and optical properties</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bendler, John T</creatorcontrib><creatorcontrib>Boyles, David A</creatorcontrib><creatorcontrib>Edmondson, Charles A</creatorcontrib><creatorcontrib>Filipova, Tsvetanka</creatorcontrib><creatorcontrib>Fontanella, John J</creatorcontrib><creatorcontrib>Westgate, Mark A</creatorcontrib><creatorcontrib>Wintersgill, M. C</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bendler, John T</au><au>Boyles, David A</au><au>Edmondson, Charles A</au><au>Filipova, Tsvetanka</au><au>Fontanella, John J</au><au>Westgate, Mark A</au><au>Wintersgill, M. C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dielectric Properties of Bisphenol A Polycarbonate and Its Tethered Nitrile Analogue</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2013-05-28</date><risdate>2013</risdate><volume>46</volume><issue>10</issue><spage>4024</spage><epage>4033</epage><pages>4024-4033</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>The relative permittivity and dielectric strength have been determined for a bisphenol A polycarbonate (BPA-PC), in which a cyanoethyl group has been substituted for one of the geminal dimethyl groups. The new material (CN-PC) has a glass transition temperature that is 19 K higher than that for BPA-PC. In addition, the dielectric strength of CN-PC, 405 V/μm, is somewhat smaller than that for BPA-PC, 620 V/μm. The relative permittivity was determined from 10 to 105 Hz over a wide temperature range and at pressures up to 0.25 GPa. While the real part of the relative permittivity at 103 Hz and room temperature for BPA-PC is about 3, that for CN-PC is found to be greater than 4. Correspondingly, the γ relaxation region in CN-PC is very strong. For the γ relaxation, a strong increase in peak height as temperature increases and a strong decrease in peak height as pressure increases are observed. A relaxation is found at temperatures higher than the γ relaxation. This process is labeled as the β relaxation because it appears to be related to the β relaxation in BPA-PC in that the strength and position depend on the history of the material. The effects of pressure on the γ relaxation for both CN-PC and BPA-PC are quite large and similar to those previously seen for the γ relaxation in a fluorinated tetraaryl bisphenol A polycarbonate (DiF p-TABPA-PC). In fact, the activation volume is found to be approximately the same for all three BPA-PC-based materials despite wide variations in both peak position and peak height. Finally, computer studies of the model compounds, 4,4′-diphenylpentanenitrile and diphenyl carbonate, were carried out. Both provide insight into the nature of the γ relaxation with the latter yielding an activation volume in approximate agreement with the experimental values.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma4002269</doi><tpages>10</tpages></addata></record> |
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title | Dielectric Properties of Bisphenol A Polycarbonate and Its Tethered Nitrile Analogue |
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