Reaction rate and MWD changes in crosslinking of PVC, with dithioltriazine

Abstract

AbstractThe reaction rate of crosslinking of PVC with dithioltriazine has been studied by following gel formation and changes in the molecular weight distribution (MWD). Compounding was performed on a roll mill at 145°C and crosslinking by heat treatment at 180 or 90°C. In this system crosslinking is executed by the thiolate anion, formed in situ by reaction with MgO. We have studied the catalyzing effect of several polyols in order to achieve a more efficient reaction. Most likely, these catalysts work by chelating the Mg2+ ions, thus increasing the nucleophilic character of the thiolate. With the most efficient ones, ditrimethylolpropane and HO(CH2CH2)6‐7H, complete crosslinking can be obtained in 3 min at 180°C, i.e., at processing temperatures. We also followed the changes in the MWD before gelation at a considerably lower temperature, 145°C, and found an extensive molecular enlargement even after 5‐10 min. Most surprisingly, μMn increased up to 100% without formation of insoluble material. By 1H‐NMR measurements on low molecular weight extracts, we have shown this to be due to a fast and selective reaction with allylic chlorine in the unsaturated end groups, ∼ CH2CHCHCH2Cl, formed in the mechanism of chain transfer to monomer. Due to this reaction, formulations with too high reactivity may crosslink during processing, which calls for a careful balancing of the reactivity for each processing case.