gel-fraction

Chemical Modification of Polyglycidyl Phenol-Formaldehyde Oligomers by Methacrylic Acid

A new oligomer with unsaturated double bonds in the side chains has been synthesized via chemical modification of polyglycidyl phenol-formaldehyde oligomers (PGPFO) by methacrylic acid (MA) using benzyltriethylammonium chloride as a catalyst. The effect of temperature and reaction time on the reaction proceeded between PGPFO and MA has been studied. The effective rate constants and activation energy of the reaction have been calculated. The structure of the synthesized oligomer has been confirmed by chemical and IR-spectroscopic analyses.

Ammonia-free, Low-toxic Press-materials with Improved Electroinsulating Properties Based on Modified Novolak Phenol-formaldehyde Resin

The technological and operational properties of press-materials based on novolak composition modified jointly by epoxydianic resin and polyvinylpyrrolidone depending upon filler nature and pressing conditions have been determined. The reactivity of obtained press-powders has been investigated depending upon filler type, as well as curing conditions of composites under which ammonia and formaldehyde are not emitted.

Synthesis and Properties of Carboxy-Containing Peroxy Oligomer

Carboxy-containing peroxy oligomer (CPO) has been synthesized via the reaction of peroxy derivative of ED-24 epoxy resin with free peroxy and epoxy groups with adipic acid in the presence of benzyl triethylammonium chloride. The effect of catalyst amount, reaction temperature and process time on the reaction rate has been determined. The effective rate constants and activation energies have been calculated. CPO synthesis procedure has been developed. CPO structure has been confirmed by chemical and IR-spectroscopic analyses.