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Phase structure and properties of poly(ethylene terephthalate)/high‐density polyethylene based on recycled materials
Authors:Yong Lei  Qinglin Wu  Craig M Clemons  Weihong Guo
Affiliation:1. School of Renewable Natural Resources, Louisiana State University Agricultural Center, Baton Rouge, Louisiana 70803;2. Performance Engineered Composites, USDA Forest Service, Forest Products Laboratory, One Gifford Pinchot Drive, Madison, Wisconsin 53705‐2398;3. Polymer Alloy Laboratory, Department of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, People's Republic of China
Abstract:Blends based on recycled high density polyethylene (R‐HDPE) and recycled poly(ethylene terephthalate) (R‐PET) were made through reactive extrusion. The effects of maleated polyethylene (PE‐g‐MA), triblock copolymer of styrene and ethylene/butylene (SEBS), and 4,4′‐methylenedi(phenyl isocyanate) (MDI) on blend properties were studied. The 2% PE‐g‐MA improved the compatibility of R‐HDPE and R‐PET in all blends toughened by SEBS. For the R‐HDPE/R‐PET (70/30 w/w) blend toughened by SEBS, the dispersed PET domain size was significantly reduced with use of 2% PE‐g‐MA, and the impact strength of the resultant blend doubled. For blends with R‐PET matrix, all strengths were improved by adding MDI through extending the PET molecular chains. The crystalline behaviors of R‐HDPE and R‐PET in one‐phase rich systems influenced each other. The addition of PE‐g‐MA and SEBS consistently reduced the crystalline level (χc) of either the R‐PET or the R‐HDPE phase and lowered the crystallization peak temperature (Tc) of R‐PET. Further addition of MDI did not influence R‐HDPE crystallization behavior but lowered the χc of R‐PET in R‐PET rich blends. The thermal stability of R‐HDPE/R‐PET 70/30 and 50/50 (w/w) blends were improved by chain‐extension when 0.5% MDI was added. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009
Keywords:polyethylene  recycling  blends  poly(ethylene terephthalate)
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