oligoesteracrylate

A monocarboxylic derivative of Epidian-6 with free epoxy and carboxylic end groups (MCDER) has been synthesized using Epidian-6 epoxy resin and sebacic acid. The structure of MCDER was confirmed by a spectral analysis. The thermal stability of MCDER has been established and the formation of cross-linked films based on epoxy-oligomeric mixtures consisting of Epidian-5, TGM-3 oligoesteracrylate, and polyethylene polyamine has been studied in its presence. By means of IR spectroscopy, the chemistry of the mixtures formation has been established.

Physico-mechanical properties of the products based on filled epoxy-oligomeric mixtures composed of Epidian-5 epoxy resin, oligoesteracrylate TGM-3 and monoperoxide derivative of Epidian-6 epoxy resin (PO) have been investigated. CaCO3 was used as a filler and polyethylene polyamine was a curing agent. The effect of PO and CaCO3 on the gel-fraction content and physico-mechanical properties was examined. Using a scanning electron microscopy (SEM) the morphology of the samples has been studied.

Crosslinking of epoxy-oligoesteric mixtures composed of ED-20 dianic epoxy resin and TGM-3 oligoesteracrylate has been studied in the presence of dioxydiphenylpropane diglycidyl ether modified with adipic acid (DCDER). Crosslinking was carried out at room temperature and while heating at 383, 403 or 423 K using polyethylene polyamine as a hardener. The procedure of DCDER synthesis has been developed. The structural changes were controlled by determining film hardness and gel-fraction content. The chemistry of films formation was confirmed by IR-spectroscopy. 

Crosslinking of epoxy-oligomeric mixtures has been studied at room temperature and at heating to 383, 403 and 423 K for 15, 30, 45, 60 and 75 min in the presence of polyethylenepolyamine. The mixtures consist of industrial ED-20 epoxy resin, oligoesteracrylate TGM-3 and carboxy-containing derivative of ED-24 epoxy resin. The effect of mixture composition, temperature and process time on the gel-fraction content and hardness of polymeric films has been examined. Using IR-spectroscopy the chemism of network formation has been determined.

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.

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.