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Oxidative degradations of oxodegradable LDPE enhanced with thermoplastic pea starch: Thermo‐mechanical properties, morphology, and UV‐ageing studies
Author(s) -
Raquez JeanMarie,
Bourgeois Audrey,
Jacobs Heidi,
Degée Philippe,
Alexandre Michael,
Dubois Philippe
Publication year - 2011
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.34190
Subject(s) - low density polyethylene , materials science , thermoplastic , differential scanning calorimetry , composite material , ultimate tensile strength , fourier transform infrared spectroscopy , thermogravimetric analysis , starch , polyethylene , dynamic mechanical analysis , melt flow index , copolymer , chemical engineering , polymer , chemistry , organic chemistry , physics , engineering , thermodynamics
The abiotic UV‐degradation behavior of oxodegradable LDPE was investigated in the presence of thermoplastic pea starch (TPPS) in this study. Oxodegradable LDPE was first melt‐blended with thermoplastic pea starch (TPPS) using an internal mixing chamber to enhance the abiotic oxidative degradation of oxodegradable LDPE. Because of their different affinity, maleated polyethylene was added as compatibilizer. Tensile properties, thermal properties, and morphology of resulting melt‐blends were determined at different content in TPPS. High content in TPPS (40 wt %) could be readily added to oxodegradable LDPE without affecting the tensile properties of resulting melt‐blends. UV‐ageing studies on compatibilized TPPS/oxodegradable LDPE melt‐blends were carried out by Attenuated Total Reflectance infrared spectroscopy (ATR‐FTIR), Dynamic Thermomechanical Analyses (DMTA) and Differential Scanning Calorimetry (DSC) under abiotic conditions. These results suggested a synergistic effect on the UV‐ageing of TPPS‐based melt‐blends provided by both components during the first stage of UV‐irradiation. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.