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Photo-stabilising action of metal chelates in polypropylene—Part II: Photolysis versus photo-sensitised oxidation under monochromatic irradiation
Authors:Norman S Allen  Alfonso Chirinos-Padron  John H Appleyard
Institution:1. Department of Chemistry. John Dalton Faculty of Technology, Manchester Polytechnic, Chester Street, Manchester M1 5GD, Great Britain;2. Department of Physics, Mathematics and Computing. John Dalton Faculty of Technology, Manchester Polytechnic, Chester Street, Manchester M1 5GD, Great Britain
Abstract:The photo-stabilising action of three metal chelates in unprocessed and processed polypropylene is examined using normal and second order derivative ultraviolet and infra-red spectroscopic techniques and hydroperoxide analysis. The effects of photolysis with 254 nm light versus photo-sensitised oxidation with 365 nm light are compared. For each exposure condition the rate of carbonyl formation in the polymer is compared with the rate of decomposition of the metal complex. On photolysis, carbonyl growth commences well before the complete destruction of the complexes and none offers protection to the polymer. In fact, all three chelates behave as photo-sensitisers, indicating that stabiliser photolysis products are photo-active. On photo-sensitised oxidation, while the initial hydroperoxide concentration appears to control the onset of carbonyl growth in the polymer, the rate of decomposition of the complexes shows no dependence on hydroperoxide concentration. Solution experiments indicate that there are no dark reactions with hydroperoxides apart from one of the nickel chelates (Cyasorb UV 1084) at high concentrations (~ 10?2m) only. Essentially, the metal chelates operate by scavenging macroalkyl radical species (P·) and not alkoxy (PO·) and hydroxy radicals (·OH) during photo-oxidation. They also inhibit hydroperoxide formation during processing and one of the nickel chelates (UV 1084) gives products during the early stages of photo-oxidation which appear to operate as effective stabilisers.
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