๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Mechanism of the photo-oxidation of polyethylene

โœ Scribed by C.H. Chew; L.M. Gan; G. Scott


Publisher
Elsevier Science
Year
1977
Tongue
English
Weight
272 KB
Volume
13
Category
Article
ISSN
0014-3057

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstraet--The mechanism of the photo-oxidation of both low density and high density polyethylenes has been studied kinetically. The kinetics are consistent with the view that when substantial quantities of carbonyl compounds are present in the polymers by photolysis of thermally formed hydroperoxides. they are intimately involved as initiators in the photo-oxidation by Norrish I photolysis of ketones The latter process is also responsible for the ultimate end products of photo-oxidation, viz. carboxylic acids. The two polymers differ in that cross-linking occurs initially in LDPE with reduction in vinylidene unsaturation whereas chain scission predominates in HDPE.

The effect of iron compounds is in accord with their behaviour in thermal oxidation. Iron carboxylares activate both types of polyethylene to photo-oxidation primarily by decreasing the amount of carbonyl compounds present, although initially they also generate radicals by photolysis. The iron dithiocarbamates on the other hand are initially antioxidants and initially prevent carbonyl formation in the polymer. They function as photo-activators primarily by photolysis to free radicals


๐Ÿ“œ SIMILAR VOLUMES


Mechanism of polyethylene oxidation
โœ E. M. Bevilacqua; E. S. English; J. S. Gall ๐Ÿ“‚ Article ๐Ÿ“… 1964 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 380 KB ๐Ÿ‘ 1 views
Photo-initiated oxidation of polyethylen
โœ M.U. Amin; G. Scott ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 669 KB

Al~traet--Several important classes of u.v. activator for polymers have been studied in polyethylene. The progress of the oxidation was followed by measuring earbonyl formation in polyethylene films (carbonyl index) and by following the change in dynamic modulus of the polymer with time. The two pro