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Graft-interpenetrating polymer networks of epoxy with polyurethanes derived from poly(ethyleneterephthalate) waste
ABSTRACT Polyester polyurethanes derived from poly(ethyleneterephthalate) (PET) glycolysates were blended with epoxy to form graft‐interpenetrating networks (IPNs) with improved mechanical properties. Microwave‐assisted glycolytic depolymerization of PET was performed in the presence of polyethylene...
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Published in: | Journal of applied polymer science 2014-07, Vol.131 (13), p.np-n/a |
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creator | Chaudhary, Saurabh Parthasarathy, Surekha Kumar, Devendra Rajagopal, Chitra Roy, Prasun Kumar |
description | ABSTRACT
Polyester polyurethanes derived from poly(ethyleneterephthalate) (PET) glycolysates were blended with epoxy to form graft‐interpenetrating networks (IPNs) with improved mechanical properties. Microwave‐assisted glycolytic depolymerization of PET was performed in the presence of polyethylene glycols of different molecular weights (600–1500). The resultant hydroxyl terminated polyester was used for synthesis of polyurethane prepolymer which was subsequently reacted with epoxy resin to generate grafted structures. The epoxy‐polyurethane blend was cured with triethylene tetramine under ambient conditions to result in graft IPNs. Blending resulted in an improvement in the mechanical properties, the extent of which was found to be dependant both on the amount as well as molecular weight of PET‐based polyurethane employed. Maximum improvement was observed in epoxy blends prepared with polyurethane (PU1000) at a loading of 10% w/w which resulted in 61% increase in tensile strength and 212% increase in impact strength. The extent of toughening was quantified by flexural studies under single edge notch bending (SENB) mode. In comparison to the unmodified epoxy, the Mode I fracture toughness (KIC) and fracture energy (GIC) increased by ∼45% and ∼184%, respectively. The underlying toughening mechanisms were identified by fractographic analysis, which generated evidence of rubber cavitation, microcracking, and crack path deflection. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40490. |
doi_str_mv | 10.1002/app.40490 |
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Polyester polyurethanes derived from poly(ethyleneterephthalate) (PET) glycolysates were blended with epoxy to form graft‐interpenetrating networks (IPNs) with improved mechanical properties. Microwave‐assisted glycolytic depolymerization of PET was performed in the presence of polyethylene glycols of different molecular weights (600–1500). The resultant hydroxyl terminated polyester was used for synthesis of polyurethane prepolymer which was subsequently reacted with epoxy resin to generate grafted structures. The epoxy‐polyurethane blend was cured with triethylene tetramine under ambient conditions to result in graft IPNs. Blending resulted in an improvement in the mechanical properties, the extent of which was found to be dependant both on the amount as well as molecular weight of PET‐based polyurethane employed. Maximum improvement was observed in epoxy blends prepared with polyurethane (PU1000) at a loading of 10% w/w which resulted in 61% increase in tensile strength and 212% increase in impact strength. The extent of toughening was quantified by flexural studies under single edge notch bending (SENB) mode. In comparison to the unmodified epoxy, the Mode I fracture toughness (KIC) and fracture energy (GIC) increased by ∼45% and ∼184%, respectively. The underlying toughening mechanisms were identified by fractographic analysis, which generated evidence of rubber cavitation, microcracking, and crack path deflection. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40490.</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.40490</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken, NJ: Blackwell Publishing Ltd</publisher><subject>Applied sciences ; Blends ; Exact sciences and technology ; Fracture mechanics ; Grafting ; Materials science ; mechanical properties ; Networks ; Polyester resins ; polyesters ; Polyethylene terephthalates ; Polymer industry, paints, wood ; Polymers ; Polyurethane resins ; polyurethanes ; Technology of polymers ; Toughening ; Waste treatment</subject><ispartof>Journal of applied polymer science, 2014-07, Vol.131 (13), p.np-n/a</ispartof><rights>Copyright © 2014 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3980-5a126ff78b73311b736bb49e6abb8cc22c68b65ab80b966f3e10f29ab54d5ce33</citedby><cites>FETCH-LOGICAL-c3980-5a126ff78b73311b736bb49e6abb8cc22c68b65ab80b966f3e10f29ab54d5ce33</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=28417031$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Chaudhary, Saurabh</creatorcontrib><creatorcontrib>Parthasarathy, Surekha</creatorcontrib><creatorcontrib>Kumar, Devendra</creatorcontrib><creatorcontrib>Rajagopal, Chitra</creatorcontrib><creatorcontrib>Roy, Prasun Kumar</creatorcontrib><title>Graft-interpenetrating polymer networks of epoxy with polyurethanes derived from poly(ethyleneterephthalate) waste</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>ABSTRACT
Polyester polyurethanes derived from poly(ethyleneterephthalate) (PET) glycolysates were blended with epoxy to form graft‐interpenetrating networks (IPNs) with improved mechanical properties. Microwave‐assisted glycolytic depolymerization of PET was performed in the presence of polyethylene glycols of different molecular weights (600–1500). The resultant hydroxyl terminated polyester was used for synthesis of polyurethane prepolymer which was subsequently reacted with epoxy resin to generate grafted structures. The epoxy‐polyurethane blend was cured with triethylene tetramine under ambient conditions to result in graft IPNs. Blending resulted in an improvement in the mechanical properties, the extent of which was found to be dependant both on the amount as well as molecular weight of PET‐based polyurethane employed. Maximum improvement was observed in epoxy blends prepared with polyurethane (PU1000) at a loading of 10% w/w which resulted in 61% increase in tensile strength and 212% increase in impact strength. The extent of toughening was quantified by flexural studies under single edge notch bending (SENB) mode. In comparison to the unmodified epoxy, the Mode I fracture toughness (KIC) and fracture energy (GIC) increased by ∼45% and ∼184%, respectively. The underlying toughening mechanisms were identified by fractographic analysis, which generated evidence of rubber cavitation, microcracking, and crack path deflection. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40490.</description><subject>Applied sciences</subject><subject>Blends</subject><subject>Exact sciences and technology</subject><subject>Fracture mechanics</subject><subject>Grafting</subject><subject>Materials science</subject><subject>mechanical properties</subject><subject>Networks</subject><subject>Polyester resins</subject><subject>polyesters</subject><subject>Polyethylene terephthalates</subject><subject>Polymer industry, paints, wood</subject><subject>Polymers</subject><subject>Polyurethane resins</subject><subject>polyurethanes</subject><subject>Technology of polymers</subject><subject>Toughening</subject><subject>Waste treatment</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kEFvEzEQhS0EEqFw4B-shJDaw7b2eu21j1UoAamUHAocLdsZE7eb9WI7Tfff4yalB6RextK87z2PHkLvCT4lGDdnehxPW9xK_ALNCJZd3fJGvESzopFaSMleozcp3WBMCMN8huIiapdrP2SIIwyQo85--F2NoZ82EKuy2YV4m6rgKhjD_VTtfF7v5W2EvNYDpGoF0d_BqnIxbPbScVGm_iEOIozrgvU6w0m10ynDW_TK6T7Bu8f3CP34fHE9_1Jffl98nZ9f1pZKgWumScOd64TpKCWkTG5MK4FrY4S1TWO5MJxpI7CRnDsKBLtGasPaFbNA6RE6PuSOMfzZQspq45OFvi83h21ShFFcPhJMFPTDf-hN2MahXFco0lDadVwW6uRA2RhSiuDUGP1Gx0kRrB7aV6V9tW-_sB8fE3WyundRD9anJ0MjWtJhSgp3duB2vofp-UB1vlz-S64PDl-6vH9y6HireEc7pn5dLRT_ef1p_m2JFaV_AV0tpOw</recordid><startdate>20140705</startdate><enddate>20140705</enddate><creator>Chaudhary, Saurabh</creator><creator>Parthasarathy, Surekha</creator><creator>Kumar, Devendra</creator><creator>Rajagopal, Chitra</creator><creator>Roy, Prasun Kumar</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20140705</creationdate><title>Graft-interpenetrating polymer networks of epoxy with polyurethanes derived from poly(ethyleneterephthalate) waste</title><author>Chaudhary, Saurabh ; Parthasarathy, Surekha ; Kumar, Devendra ; Rajagopal, Chitra ; Roy, Prasun Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3980-5a126ff78b73311b736bb49e6abb8cc22c68b65ab80b966f3e10f29ab54d5ce33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Applied sciences</topic><topic>Blends</topic><topic>Exact sciences and technology</topic><topic>Fracture mechanics</topic><topic>Grafting</topic><topic>Materials science</topic><topic>mechanical properties</topic><topic>Networks</topic><topic>Polyester resins</topic><topic>polyesters</topic><topic>Polyethylene terephthalates</topic><topic>Polymer industry, paints, wood</topic><topic>Polymers</topic><topic>Polyurethane resins</topic><topic>polyurethanes</topic><topic>Technology of polymers</topic><topic>Toughening</topic><topic>Waste treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chaudhary, Saurabh</creatorcontrib><creatorcontrib>Parthasarathy, Surekha</creatorcontrib><creatorcontrib>Kumar, Devendra</creatorcontrib><creatorcontrib>Rajagopal, Chitra</creatorcontrib><creatorcontrib>Roy, Prasun Kumar</creatorcontrib><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 applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chaudhary, Saurabh</au><au>Parthasarathy, Surekha</au><au>Kumar, Devendra</au><au>Rajagopal, Chitra</au><au>Roy, Prasun Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Graft-interpenetrating polymer networks of epoxy with polyurethanes derived from poly(ethyleneterephthalate) waste</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2014-07-05</date><risdate>2014</risdate><volume>131</volume><issue>13</issue><spage>np</spage><epage>n/a</epage><pages>np-n/a</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>ABSTRACT
Polyester polyurethanes derived from poly(ethyleneterephthalate) (PET) glycolysates were blended with epoxy to form graft‐interpenetrating networks (IPNs) with improved mechanical properties. Microwave‐assisted glycolytic depolymerization of PET was performed in the presence of polyethylene glycols of different molecular weights (600–1500). The resultant hydroxyl terminated polyester was used for synthesis of polyurethane prepolymer which was subsequently reacted with epoxy resin to generate grafted structures. The epoxy‐polyurethane blend was cured with triethylene tetramine under ambient conditions to result in graft IPNs. Blending resulted in an improvement in the mechanical properties, the extent of which was found to be dependant both on the amount as well as molecular weight of PET‐based polyurethane employed. Maximum improvement was observed in epoxy blends prepared with polyurethane (PU1000) at a loading of 10% w/w which resulted in 61% increase in tensile strength and 212% increase in impact strength. The extent of toughening was quantified by flexural studies under single edge notch bending (SENB) mode. In comparison to the unmodified epoxy, the Mode I fracture toughness (KIC) and fracture energy (GIC) increased by ∼45% and ∼184%, respectively. The underlying toughening mechanisms were identified by fractographic analysis, which generated evidence of rubber cavitation, microcracking, and crack path deflection. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40490.</abstract><cop>Hoboken, NJ</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1002/app.40490</doi><tpages>9</tpages></addata></record> |
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subjects | Applied sciences Blends Exact sciences and technology Fracture mechanics Grafting Materials science mechanical properties Networks Polyester resins polyesters Polyethylene terephthalates Polymer industry, paints, wood Polymers Polyurethane resins polyurethanes Technology of polymers Toughening Waste treatment |
title | Graft-interpenetrating polymer networks of epoxy with polyurethanes derived from poly(ethyleneterephthalate) waste |
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