Highly phosphonated poly(N-phenylacrylamide) for proton exchange membranes
A novel highly phosphonated poly(N-phenylacrylamide) (PDPAA) with an ion-exchange capacity (IEC) of 6.72 mequiv/g was synthesized by the radical polymerization of N-[2,4-bis(diethoxyphosphinoyl)phenyl]acrylamide (DEPAA), followed by the hydrolysis with trimethylsilyl bromide. Then, the crosslinked P...
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creator | Fukuzaki, Namiko Nakabayashi, Kazuhiro Nakazawa, Satoshi Murata, Shigeaki Higashihara, Tomoya Ueda, Mitsuru |
description | A novel highly phosphonated poly(N-phenylacrylamide) (PDPAA) with an ion-exchange capacity (IEC) of 6.72 mequiv/g was synthesized by the radical polymerization of N-[2,4-bis(diethoxyphosphinoyl)phenyl]acrylamide (DEPAA), followed by the hydrolysis with trimethylsilyl bromide. Then, the crosslinked PDPAA membrane was successfully prepared by the electrophilic substitution reaction between the aromatic rings of PDPAA and the carbocation formed from hexamethoxymethylmelamine (CYMEL) as a crosslinker in the presence of methanesulfonic acid. The crosslinked PDPAA membrane had high oxidative stability against Fenton's reagent at room temperature. The proton conductivity of the crosslinked PDPAA membrane was 8.8 × 10⁻² S/cm at 95% relative humidity (RH) and 80 °C, which was comparable to Nafion 112. Under low RH, the crosslinked PDPAA membrane showed the proton conductivity of 1.9 × 10⁻³ and 4.7 × 10⁻⁵ S/cm at 50 and 30% RH, respectively. The proton conductivity of the crosslinked PDPAA membrane lied in the highest class among the reported phosphonated polymers, and, consequently, the very high local concentration of the acids of PDPAA (IEC = 6.72 mequiv/g) achieved high and effective proton conduction under high RH. |
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Then, the crosslinked PDPAA membrane was successfully prepared by the electrophilic substitution reaction between the aromatic rings of PDPAA and the carbocation formed from hexamethoxymethylmelamine (CYMEL) as a crosslinker in the presence of methanesulfonic acid. The crosslinked PDPAA membrane had high oxidative stability against Fenton's reagent at room temperature. The proton conductivity of the crosslinked PDPAA membrane was 8.8 × 10⁻² S/cm at 95% relative humidity (RH) and 80 °C, which was comparable to Nafion 112. Under low RH, the crosslinked PDPAA membrane showed the proton conductivity of 1.9 × 10⁻³ and 4.7 × 10⁻⁵ S/cm at 50 and 30% RH, respectively. The proton conductivity of the crosslinked PDPAA membrane lied in the highest class among the reported phosphonated polymers, and, consequently, the very high local concentration of the acids of PDPAA (IEC = 6.72 mequiv/g) achieved high and effective proton conduction under high RH.</description><identifier>ISSN: 0887-624X</identifier><identifier>ISSN: 1099-0518</identifier><identifier>EISSN: 1099-0518</identifier><identifier>DOI: 10.1002/pola.24422</identifier><identifier>CODEN: JPLCAT</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; Crosslinking ; crosslinking reaction ; Exact sciences and technology ; Exchange resins and membranes ; Forms of application and semi-finished materials ; high-performance polymers ; Hydrolysis ; Membranes ; Organic polymers ; phosphonated polymers ; Physicochemistry of polymers ; polyacrylamides ; polymer electrolyte fuel cells ; polymer electrolyte membranes ; Polymer industry, paints, wood ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Proton conduction ; proton conductivity ; radical polymerization ; Radicals ; Relative humidity ; Reproduction ; Stability ; Technology of polymers</subject><ispartof>Journal of polymer science. Part A, Polymer chemistry, 2011, Vol.49 (1), p.93-100</ispartof><rights>Copyright © 2010 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3972-cbaa31285b5533f7ad63dacaf43d5fa1794232dbba286460594143df3dd0938f3</citedby><cites>FETCH-LOGICAL-c3972-cbaa31285b5533f7ad63dacaf43d5fa1794232dbba286460594143df3dd0938f3</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%2Fpola.24422$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpola.24422$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23750930$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Fukuzaki, Namiko</creatorcontrib><creatorcontrib>Nakabayashi, Kazuhiro</creatorcontrib><creatorcontrib>Nakazawa, Satoshi</creatorcontrib><creatorcontrib>Murata, Shigeaki</creatorcontrib><creatorcontrib>Higashihara, Tomoya</creatorcontrib><creatorcontrib>Ueda, Mitsuru</creatorcontrib><title>Highly phosphonated poly(N-phenylacrylamide) for proton exchange membranes</title><title>Journal of polymer science. Part A, Polymer chemistry</title><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><description>A novel highly phosphonated poly(N-phenylacrylamide) (PDPAA) with an ion-exchange capacity (IEC) of 6.72 mequiv/g was synthesized by the radical polymerization of N-[2,4-bis(diethoxyphosphinoyl)phenyl]acrylamide (DEPAA), followed by the hydrolysis with trimethylsilyl bromide. Then, the crosslinked PDPAA membrane was successfully prepared by the electrophilic substitution reaction between the aromatic rings of PDPAA and the carbocation formed from hexamethoxymethylmelamine (CYMEL) as a crosslinker in the presence of methanesulfonic acid. The crosslinked PDPAA membrane had high oxidative stability against Fenton's reagent at room temperature. The proton conductivity of the crosslinked PDPAA membrane was 8.8 × 10⁻² S/cm at 95% relative humidity (RH) and 80 °C, which was comparable to Nafion 112. Under low RH, the crosslinked PDPAA membrane showed the proton conductivity of 1.9 × 10⁻³ and 4.7 × 10⁻⁵ S/cm at 50 and 30% RH, respectively. The proton conductivity of the crosslinked PDPAA membrane lied in the highest class among the reported phosphonated polymers, and, consequently, the very high local concentration of the acids of PDPAA (IEC = 6.72 mequiv/g) achieved high and effective proton conduction under high RH.</description><subject>Applied sciences</subject><subject>Crosslinking</subject><subject>crosslinking reaction</subject><subject>Exact sciences and technology</subject><subject>Exchange resins and membranes</subject><subject>Forms of application and semi-finished materials</subject><subject>high-performance polymers</subject><subject>Hydrolysis</subject><subject>Membranes</subject><subject>Organic polymers</subject><subject>phosphonated polymers</subject><subject>Physicochemistry of polymers</subject><subject>polyacrylamides</subject><subject>polymer electrolyte fuel cells</subject><subject>polymer electrolyte membranes</subject><subject>Polymer industry, paints, wood</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Proton conduction</subject><subject>proton conductivity</subject><subject>radical polymerization</subject><subject>Radicals</subject><subject>Relative humidity</subject><subject>Reproduction</subject><subject>Stability</subject><subject>Technology of polymers</subject><issn>0887-624X</issn><issn>1099-0518</issn><issn>1099-0518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kDlPxDAUhC0EEsvR8AdIgzikgI84jktAsBzLIQGCznpx7N1ALuxFkH-PIUBJYbt438wbD0IbBO8TjOlB11awT5OE0gU0IljKGHOSLaIRzjIRpzR5WkYr3j9jHGY8G6GLs3I6q_qom7U-nAbmpoiCS79zHXcz0_QVaBeuuizMbmRbF3WunbdNZD70DJqpiWpT5w4a49fQkoXKm_WfdxU9nJ7cH5_Fk5vx-fHhJNZMChrrHIARmvGcc8asgCJlBWiwCSu4BSJkQhkt8hxoliYp5jIhYWRZUWDJMstW0fbgG5K8vhk_V3XptamqEKJ980piknIpRBrIvYHUrvXeGas6V9bgekWw-upLffWlvvsK8NaPLXgNlQ1_0qX_U1AmeNiPA0cG7r2sTP-Po7q9mRz-eseDpvRz8_GnAfeiUhGM1eP1WF3c3omjy6ux4oHfHHgLrYKpCzke7igmDBNJMhF6-wQi0JNA</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Fukuzaki, Namiko</creator><creator>Nakabayashi, Kazuhiro</creator><creator>Nakazawa, Satoshi</creator><creator>Murata, Shigeaki</creator><creator>Higashihara, Tomoya</creator><creator>Ueda, Mitsuru</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>2011</creationdate><title>Highly phosphonated poly(N-phenylacrylamide) for proton exchange membranes</title><author>Fukuzaki, Namiko ; Nakabayashi, Kazuhiro ; Nakazawa, Satoshi ; Murata, Shigeaki ; Higashihara, Tomoya ; Ueda, Mitsuru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3972-cbaa31285b5533f7ad63dacaf43d5fa1794232dbba286460594143df3dd0938f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Applied sciences</topic><topic>Crosslinking</topic><topic>crosslinking reaction</topic><topic>Exact sciences and technology</topic><topic>Exchange resins and membranes</topic><topic>Forms of application and semi-finished materials</topic><topic>high-performance polymers</topic><topic>Hydrolysis</topic><topic>Membranes</topic><topic>Organic polymers</topic><topic>phosphonated polymers</topic><topic>Physicochemistry of polymers</topic><topic>polyacrylamides</topic><topic>polymer electrolyte fuel cells</topic><topic>polymer electrolyte membranes</topic><topic>Polymer industry, paints, wood</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Proton conduction</topic><topic>proton conductivity</topic><topic>radical polymerization</topic><topic>Radicals</topic><topic>Relative humidity</topic><topic>Reproduction</topic><topic>Stability</topic><topic>Technology of polymers</topic><toplevel>online_resources</toplevel><creatorcontrib>Fukuzaki, Namiko</creatorcontrib><creatorcontrib>Nakabayashi, Kazuhiro</creatorcontrib><creatorcontrib>Nakazawa, Satoshi</creatorcontrib><creatorcontrib>Murata, Shigeaki</creatorcontrib><creatorcontrib>Higashihara, Tomoya</creatorcontrib><creatorcontrib>Ueda, Mitsuru</creatorcontrib><collection>AGRIS</collection><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. Part A, Polymer chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fukuzaki, Namiko</au><au>Nakabayashi, Kazuhiro</au><au>Nakazawa, Satoshi</au><au>Murata, Shigeaki</au><au>Higashihara, Tomoya</au><au>Ueda, Mitsuru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly phosphonated poly(N-phenylacrylamide) for proton exchange membranes</atitle><jtitle>Journal of polymer science. Part A, Polymer chemistry</jtitle><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><date>2011</date><risdate>2011</risdate><volume>49</volume><issue>1</issue><spage>93</spage><epage>100</epage><pages>93-100</pages><issn>0887-624X</issn><issn>1099-0518</issn><eissn>1099-0518</eissn><coden>JPLCAT</coden><abstract>A novel highly phosphonated poly(N-phenylacrylamide) (PDPAA) with an ion-exchange capacity (IEC) of 6.72 mequiv/g was synthesized by the radical polymerization of N-[2,4-bis(diethoxyphosphinoyl)phenyl]acrylamide (DEPAA), followed by the hydrolysis with trimethylsilyl bromide. Then, the crosslinked PDPAA membrane was successfully prepared by the electrophilic substitution reaction between the aromatic rings of PDPAA and the carbocation formed from hexamethoxymethylmelamine (CYMEL) as a crosslinker in the presence of methanesulfonic acid. The crosslinked PDPAA membrane had high oxidative stability against Fenton's reagent at room temperature. The proton conductivity of the crosslinked PDPAA membrane was 8.8 × 10⁻² S/cm at 95% relative humidity (RH) and 80 °C, which was comparable to Nafion 112. Under low RH, the crosslinked PDPAA membrane showed the proton conductivity of 1.9 × 10⁻³ and 4.7 × 10⁻⁵ S/cm at 50 and 30% RH, respectively. The proton conductivity of the crosslinked PDPAA membrane lied in the highest class among the reported phosphonated polymers, and, consequently, the very high local concentration of the acids of PDPAA (IEC = 6.72 mequiv/g) achieved high and effective proton conduction under high RH.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/pola.24422</doi><tpages>8</tpages></addata></record> |
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subjects | Applied sciences Crosslinking crosslinking reaction Exact sciences and technology Exchange resins and membranes Forms of application and semi-finished materials high-performance polymers Hydrolysis Membranes Organic polymers phosphonated polymers Physicochemistry of polymers polyacrylamides polymer electrolyte fuel cells polymer electrolyte membranes Polymer industry, paints, wood Polymers with particular properties Preparation, kinetics, thermodynamics, mechanism and catalysts Proton conduction proton conductivity radical polymerization Radicals Relative humidity Reproduction Stability Technology of polymers |
title | Highly phosphonated poly(N-phenylacrylamide) for proton exchange membranes |
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