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A detailed surface analytical study of degradation processes in (meth)acrylic polymers
Authors:Alexander H Soeriyadi  Vanessa Trouillet  Francesca Bennet  Michael Bruns  Michael R Whittaker  Cyrille Boyer  Philip J Barker  Thomas P Davis  Christopher Barner‐Kowollik
Institution:1. Centre for Advanced Macromolecular Design, School of Chemical Engineering, The University of New South Wales, Sydney 2052, Australia;2. Institute for Applied Materials (IAM‐WPT), Karlsruhe Institute of Technology (KIT), 76344 Eggenstein‐Leopoldshafen, Germany;3. BlueScope Steel Research, PO BOX 202, Port Kembla, NSW 2505, Australia;4. Preparative Macromolecular Chemistry, Institut für Technische Chemie und Polymerchemie, Engesserstr. 18, Karlsruhe Institute of Technology (KIT), 76128 Karlsruhe, Germany
Abstract:The present study investigates the degradation behavior of various high‐molecular‐weight acrylic polymers (50,000 < Mn/g mol?1 < 100,000), namely poly(methyl methacrylate) (PMMA), poly(n‐butyl methacrylate) (PBMA), poly(n‐butyl acrylate) (PBA), and poly(lauryl methacrylate) (PLMA), under extreme environmental conditions. These polymers were synthesized via various polymerization techniques to create different end‐groups. The polymers chosen are readily applicable in the formulation of surface coatings and were degraded under conditions which replicate the harsh Australian climate, where surface coatings may reach temperatures of up to 95 °C and are exposed to broad‐spectrum UV radiation of up to 1 kW m?2. The degradation behavior of the polymeric materials on their surface was followed via ATR‐IR spectroscopy, high resolution FTIR microscopy, and X‐ray photoelectron spectroscopy. The extent of the observed thermal and photo‐oxidation is directly related to the length of the ester side group, with the degradation susceptibility decreasing in the order of PLMA > PBMA/PBA > PMMA, with PMMA still stable even after 5 months exposure to the harshest condition used (UV light at 95 °C). The general degradation mechanism involves the loss of the ester side groups to form methacrylic acid followed by cross‐linking. The effect of the variable end groups was found to be minimal. The results from this study are in good agreement with previous studies of low‐molecular‐weight model polymers under identical conditions. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012
Keywords:high resolution FTIR microscopy  (meth)acrylic polymers  polymer degradation  X‐ray photoelectron spectroscopy (XPS)
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