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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
Main Authors: Chaudhary, Saurabh, Parthasarathy, Surekha, Kumar, Devendra, Rajagopal, Chitra, Roy, Prasun Kumar
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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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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. 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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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