Films made from blends of poly(st)rene) (PSI and pob(vinylacetophcnone) (PVAP) {up to 12% mol PVAP) were exposed undcr high vacuum to long wave u.v. radiation 12 > 300nm). Spectral changes {phosphorescence, NMR and i.r. indicated that PVAP was photolysed: the nature of gaseous products (in order of
Photolysis of poly(p-isopropyl styrene)
β Scribed by N.A. Weir; T.H. Milkie
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- English
- Weight
- 412 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
The photodegradation of films of poly(pisopropyl styrene) with 254nm radiation at 10 -~ mbar and 25 + I Β° has been studied. The principal product is hydrogen but smaller quantities of methane and ethane and a trace of propane are also formed, indicating that the p-substituent also undergoes decomposition. Ultraviolet spectra show rapid changes, particularly in the 230-240nm region, and a long wave absorption system extending into the visible region also appears. Solubility data indicate the simultaneous occurrence of cross-linking and chain sclssion, rates of both processes being significantly greater than those for poly(styrene); these results are explicable in terms of the inductive (+ I) stabilization (due to the p-C3H~ group) of radicals formed on chain scission and of the participation of the p-C3H~ group in addition reactions. Quantum yields for the evolution of the gaseous products have been estimated.
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