Chemical oxidative degradation materials

Polyisobutylene has the chemical properties of a saturated hydrocarbon. The unsaturated end groups undergo reactions typical of a hindered olefin and are used, particularly in the case of low mol wt materials, as a route to modification eg, the introduction of amine groups to produce dispersants for lubricating oils. The in-chain unsaturation in butyl mbber is attacked by atmospheric ozone, and unless protected can lead to cracking of strained vulcanizates. Oxidative degradation, which leads to chain cleavage, is slow, and the polymers are protected by antioxidants (75). 

Due to the very flexible synthetic approach, imprinted layers are highly suitable for sensor measurements in complex mixtures Sensor coatings consisting of a carbonic-acid-imprinted sol-gel material e.g. incorporate oxidative degradation products from engine oil leading to a chemical lubricant sensor. 

In contrast to the extensive work of the pure thermal degradation of polymers, less fundamental chemical information is available on the mechanism of oxidative degradation of polymeric materials. As another point of... 

Polyisobutylene and IIR have chemical resistance expected of saturated hydrocarbons. Oxidative degradation is slow and the material may be further protected by antioxidants, for example, hindered phenols. 

The chemical and enzymatic oxidative degradation of lignin (and coal) is used to obtain not only vanillin and benzoic acid, but also other aromatics (Baciocchi et al. 1999, references therein). In principle, lignin could be a major nonfossil and renewable source of aromatic compounds, a feedstock for synthesis of useful products. The problem deserves finding new ion-radical routes to cleave lignin. At present, there is some shortage in oil, gas, and even coal, which had usually been well-available natural sources of aromatics. In the near future, biomass may (and must) replace fossil-originated materials in the manufacture of commercial carbon-based products. 

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