Modelling light stabilizers as thermal antioxidants

Light stabilizers often display some degree of antioxidant activity against thermal degradation of polymers both in the solid state and the melt. Although this capacity to date has been documented in some instances such features have not been kinetically modelled for many light stabilizers. An under...

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Veröffentlicht in:Polymer degradation and stability 2006-12, Vol.91 (12), p.3390-3396
Hauptverfasser: Zeynalov, Eldar B., Allen, Norman S.
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Sprache:eng
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Zusammenfassung:Light stabilizers often display some degree of antioxidant activity against thermal degradation of polymers both in the solid state and the melt. Although this capacity to date has been documented in some instances such features have not been kinetically modelled for many light stabilizers. An understanding of the mechanisms of this activity is crucial in polymer materials due to the close link between prior thermal behaviour and post stabilisation. This paper considers the potential antioxidant activity of three representative UV stabilizers using a model system initiated (2,2′-azo-bisisobutyronitrile, AIBN) cumene oxidation. Kinetic measurements of oxidation rates in the presence of the stabilizers showed that the antioxidant activity as well as the mechanism and mode of inhibition was different for each of the stabilizers. Thus, whilst a triazine UV absorber (Cyasorb UV 1164) did not display any antioxidant activity, a hindered phenol (Cyasorb UV 2908) operated as a peroxy radical acceptor, and a hindered amine (Cyasorb 3529) retarded the model reaction without an induction period like many HAS stabilizers. The Cyasorb 2908 revealed weak antioxidant activity with a rate constant for the addition of cumylperoxy RO 2 radicals to the functional group of the stabilizer k 7 = 10 6.2 ± 0.1 e −(3900 ± 600)/R T , however, the inhibition index f (80 °C) is significantly higher than that of the commercial phenolic antioxidant Irganox 1076. Oxidation rate profiles in the presence of Cyasorb 3529 displayed a strong retarding activity by the stabilizer under conditions of the model experiments. The rates were found to depend linearly on the reciprocal square root of the concentration of the stabilizer over a sufficiently wide range thereby fitting the mechanism for the addition of cumylalkyl R radicals to the Cyasorb molecules. The rate constants for the addition of cumyl R radicals to the Cyasorb were determined to be k (333–353 K) = (2.0 ± 0.8) × 10 8 M −1 s −1. This value surpasses even the rate constants for other related HAS Chimassorb [Zeynalov EB, Allen NS. Effect of micron and nano-grade titanium dioxides on the efficiency of hindered piperidine stabilizers in a model oxidative reaction. Polym Degrad Stab 2006;91(4):931–9.] stabilizers and it follows that Cyasorb 3529 is a powerful retarder of thermal oxidation.
ISSN:0141-3910
1873-2321
DOI:10.1016/j.polymdegradstab.2006.05.020