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New Phosphonated Methacrylates: Synthesis, Photocuring and Study of their Thermal and Flame-Retardant Properties
In this work, a new methacrylate phosphonate monomer synthesis was described according to two routes: firstly, by condensation of methacrylic acid with a phosphonate epoxide and secondly by an esterification between methacryloyl chloride and a phosphonate diol. The photoinduced polymerization of thi...
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Published in: | Macromolecular chemistry and physics 2003-10, Vol.204 (15), p.1842-1850 |
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container_title | Macromolecular chemistry and physics |
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creator | Youssef, Boulos Lecamp, Laurence Khatib, Wassef El Bunel, Claude Mortaigne, Bruno |
description | In this work, a new methacrylate phosphonate monomer synthesis was described according to two routes: firstly, by condensation of methacrylic acid with a phosphonate epoxide and secondly by an esterification between methacryloyl chloride and a phosphonate diol. The photoinduced polymerization of this new monomer was studied as a function of reaction temperature. The optimal conversion of the photopolymerization was 81% for temperatures below 60 °C. Above 60 °C, the existence of a thermal polymerization leads to a decrease in the apparent photochemical yield. This new monomer is less reactive than the commercial dimethacrylate polyether of Bisphenol A we have used for copolymerization. Mechanical and thermal properties of the final copolymers were studied as a function of methacrylate phosphonate monomer content. Tg of the copolymers reaches a maximum when the phosphorus content is about 2%. The addition of phosphorus leads to an improvement of the thermal and flame‐retardant properties. Thus, addition of 2% phosphorus allows us to decrease the degradation rate, to increase the amount of remaining residue after combustion up to 12%, and finally to increase the Limiting Oxygen Index (LOI) from 16.8 (0% P) to 21.4 (2% P).
Synthetic routes to methacrylate phosphonated monomer. |
doi_str_mv | 10.1002/macp.200300025 |
format | article |
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Synthetic routes to methacrylate phosphonated monomer.</description><subject>Applied sciences</subject><subject>Chemical Sciences</subject><subject>Exact sciences and technology</subject><subject>flame retardance</subject><subject>LOI</subject><subject>methacrylate</subject><subject>phosphonate</subject><subject>photopolymerization</subject><subject>Physicochemistry of polymers</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Polymers and radiations</subject><issn>1022-1352</issn><issn>1521-3935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAQhiMEEqX0ytkXDkhkO2PHyYbbdsX2Q9t2-4E4WrOJTQzZJLJd2vx7EoK2vXGyx_M849EbRR8QZgjAj3dUdDMOIGCo5KvoACXHWORCvh7uwHmMQvK30Tvvfw7IHPLsIOqu9CPbVK3vqrahoEt2qUNFhevrofJf2F3fhEp76z-PWGiLB2ebH4yakt2Fh7JnrWEDYB27r7TbUf23tappp-NbHciV1AS2cW2nXbDav4_eGKq9Pvp3HkbfVl_vl2fx-vr0fLlYx4WY5zI2Mt9imkqhCXBeSoPbTOQywSQ1HFGABAJKMAMqE0xNzo3e8qLkOheZSUAcRp-muRXVqnN2R65XLVl1tlir8Q24AEQufuPAzia2cK33Tpu9gKDGbNWYrdpnOwgfJ6EjX1BtHDWF9c-W5HIu0nGJfOIeba37_0xVl4vl5uUf8eRaH_TT3iX3S6WZyKT6fnWqTm6WSbKSF-pE_AHPOZk5</recordid><startdate>200310</startdate><enddate>200310</enddate><creator>Youssef, Boulos</creator><creator>Lecamp, Laurence</creator><creator>Khatib, Wassef El</creator><creator>Bunel, Claude</creator><creator>Mortaigne, Bruno</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley</general><general>Wiley-VCH Verlag</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-5682-5410</orcidid></search><sort><creationdate>200310</creationdate><title>New Phosphonated Methacrylates: Synthesis, Photocuring and Study of their Thermal and Flame-Retardant Properties</title><author>Youssef, Boulos ; Lecamp, Laurence ; Khatib, Wassef El ; Bunel, Claude ; Mortaigne, Bruno</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3895-f59b16653ea018d5f1b73954146f2113050a0a4170ad416f92feb2cd2e937f403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Applied sciences</topic><topic>Chemical Sciences</topic><topic>Exact sciences and technology</topic><topic>flame retardance</topic><topic>LOI</topic><topic>methacrylate</topic><topic>phosphonate</topic><topic>photopolymerization</topic><topic>Physicochemistry of polymers</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Polymers and radiations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Youssef, Boulos</creatorcontrib><creatorcontrib>Lecamp, Laurence</creatorcontrib><creatorcontrib>Khatib, Wassef El</creatorcontrib><creatorcontrib>Bunel, Claude</creatorcontrib><creatorcontrib>Mortaigne, Bruno</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Macromolecular chemistry and physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Youssef, Boulos</au><au>Lecamp, Laurence</au><au>Khatib, Wassef El</au><au>Bunel, Claude</au><au>Mortaigne, Bruno</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Phosphonated Methacrylates: Synthesis, Photocuring and Study of their Thermal and Flame-Retardant Properties</atitle><jtitle>Macromolecular chemistry and physics</jtitle><addtitle>Macromol. Chem. Phys</addtitle><date>2003-10</date><risdate>2003</risdate><volume>204</volume><issue>15</issue><spage>1842</spage><epage>1850</epage><pages>1842-1850</pages><issn>1022-1352</issn><eissn>1521-3935</eissn><abstract>In this work, a new methacrylate phosphonate monomer synthesis was described according to two routes: firstly, by condensation of methacrylic acid with a phosphonate epoxide and secondly by an esterification between methacryloyl chloride and a phosphonate diol. The photoinduced polymerization of this new monomer was studied as a function of reaction temperature. The optimal conversion of the photopolymerization was 81% for temperatures below 60 °C. Above 60 °C, the existence of a thermal polymerization leads to a decrease in the apparent photochemical yield. This new monomer is less reactive than the commercial dimethacrylate polyether of Bisphenol A we have used for copolymerization. Mechanical and thermal properties of the final copolymers were studied as a function of methacrylate phosphonate monomer content. Tg of the copolymers reaches a maximum when the phosphorus content is about 2%. The addition of phosphorus leads to an improvement of the thermal and flame‐retardant properties. Thus, addition of 2% phosphorus allows us to decrease the degradation rate, to increase the amount of remaining residue after combustion up to 12%, and finally to increase the Limiting Oxygen Index (LOI) from 16.8 (0% P) to 21.4 (2% P).
Synthetic routes to methacrylate phosphonated monomer.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/macp.200300025</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5682-5410</orcidid></addata></record> |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | Applied sciences Chemical Sciences Exact sciences and technology flame retardance LOI methacrylate phosphonate photopolymerization Physicochemistry of polymers Polymerization Polymers Polymers and radiations |
title | New Phosphonated Methacrylates: Synthesis, Photocuring and Study of their Thermal and Flame-Retardant Properties |
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