The combination of a difunctional alkylating agent, either hydroxymethylben
zyl chloride or alpha,alpha'-dichloroxylene with polystyrene or high-impact
polystyrene together with a Friedel-Crafts catalyst, 2-ethylhexyldiphenylp
hosphate, and an amine to react with hydrogen chloride has been studied by
X-ray photoelectron spectroscopy. The results confirm what had been suggest
ed from previous investigations using thermogravimetric analysis; cross-lin
king of the polymer occurs as the temperature is raised and the alcohol-con
taining alkylating agent gives a greater amount of cross-linking than does
the dichloro compound. (C) 2001 Elsevier Science Ltd. All rights reserved.