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Published on: May 10, 2013
Ranking the accelerated weathering of plastic polymers
Maryam Hoseini1,2, Jess Stead1, Tom Bond1
1School of Sustainability, Civil and Environmental Engineering, University of Surrey, Stag Hill, Guildford GU2 7XH, UK. t.bond@surrey.ac.uk.
Abstract:
The timespans over which different plastics degrade in the environment are poorly understood. This study aimed to rank the degradation speed of five widespread plastic polymers-low density polyethylene (LDPE), polypropylene (PP), polystyrene (PS), polylactic acid (PLA) and polyethylene terephthalate (PET)-in terms of their physicochemical properties. Five of the six samples were plastic films with identical dimensions, which allowed the influence of morphology to be excluded, with a polyethylene carrier bag (PEB) tested for comparison. An accelerated weathering chamber was used to photochemically degrade samples over 41 days, with degradation monitored via mass loss and changes to carbonyl index, crystallinity and contact angle. The mass loss ranking was PP ≫ LDPE > PEB > PS > PLA > PET. Estimates of the time needed for complete degradation ranged from 0.27 years for PP to 1179 years for PET. Therefore, mass loss in PP proceeded more rapidly than the other polymers, which was unexpected based on previous literature and is plausibly explained by the presence of an unlisted additive which accelerated degradation. Increases in carbonyl index proceeded more rapidly in PP and LDPE than the other polymers tested. However, changes in contact angle and crystallinity did not correspond to the mass loss ranking. Therefore, monitoring the carbonyl index during accelerated weathering trials can indicate which polymers will fragment more quickly. However, alternative approaches are needed to simulate conditions where photooxidation reactions are negligible, such as the ocean floor.
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