T. V. Monakhova

Degradation kinetics of ethylene-octene copolymer/wood flour biocomposites in dependence to filler content

This article is focused on thermal oxidative degradation and biodegradation in soil of biocomposites based on ethylene-octene copolymer (EOC), filled by wood flour (from 30 to 70% wt.), in dependence to the filler content. The study of oxidative degradation of composites was carried out at two temperatures (80 and 130°C respectively). The induction period and the rates of oxidation were determined. It was concluded that as filler content raises, the induction period increases. It can be explained by the higher specific area of composites in comparison with pure EOC. However, high filled composites (60 and 70 % of the filler) are oxidized with a huge induction period because polyphenols in the filler inhibit the oxidation process. Biodegradation test under laboratory conditions was carried out to investigate the biodegradability of the material. Composites with lower filler content have lower weight loss rate. Small particles are capsulated by polymer and are isolated from moisture and microorganisms. On the other hand, at a high filling of the composite small particles stick together and act as large ones. Such filler agglomerates are connected with each other and allow microorganisms to penetrate into the composite. It was concluded as filler content raises the mass loss increases.

Copolymerization of propylene and methyl vinyl ketone with metallocene catalysts: Synthesis, properties, and thermal and photooxidation of modified polypropylene

The copolymers of propylene and methyl vinyl ketone are synthesized at 60°С by copolymerization in the propylene bulk in the presence of the polymethylaluminoxane-activated metallocene catalysts, namely, the isospecific С2-symmetric metallocene catalyst rac-Me2Si(2-Me-4-PhInd)2ZrCl2 and the syndiospecific Сs-symmetric metallocene catalyst Ph2ССpFluZrCl2, and characterized. It is shown that a noticeable insertion of methyl vinyl ketone into a polypropylene chain is possible during copolymerization initiated by the syndiospecific catalytic system, whereas in the case of the isospecific system, the insertion of methyl vinyl ketone is hindered. The thermal oxidation of the resulting polymers is studied. With the use of chemiluminescence, the accumulation of peroxy macroradicals under the action of daylight in samples based on isotactic and syndiotactic polypropylene is detected. It is found that even a low (0.2 mol %) content of methyl vinyl ketone endows polypropylene with the capability to undergo rapid and controlled degradation under natural conditions.