Preparation and properties of biodegradable polymeric blends from poly(propylene carbonate) and poly(ethylene-co-vinyl alcohol).

Biodegradable blends of poly(propylene carbonate)/ethylene-vinyl alcohol copolymers (PPC/EVOH) were melt prepared. The mechanical strength, crystallization and melting behavior, morphologies, and thermal properties of these blends were fully investigated using tensile tester, modulated differential scanning calorimetry, scanning electron microscopy, and thermogravimetric analysis, respectively. The results indicated that the thermal stability of blends could be enhanced by increasing EVOH content. No change was observed for the tensile strength when EVOH content was lower than 30 wt %. The tensile strength, however, increased obviously with increasing EVOH content when EVOH content was higher than 30 wt %. The crystallization behavior of the PPC/EVOH blends was studied accordingly. The degradability test showed that the weight loss of PPC/EVOH blends increased with increasing EVOH content because of the strong moisture sorption of EVOH. Morphology observation indicated that the PPC/EVOH blends exhibited a two-phase microstructure. The blends with EVOH contents ranging from 40 to 60 wt % showed the best comprehensive properties as biodegradable thermoplastic for many applications.

Enhanced wear performance of ultra high molecular weight polyethylene crosslinked by organosilane.

Ultra high molecular weight polyethylene (UHMWPE) crosslinked by organosilane was thermal compression molded. The organosilane used was the tri-ethyloxyl vinyl silane. Its gelation, melting behavior, crystallinity, mechanical and wear-resisting properties were systematically investigated. The results showed that the gel ratio of UHMWPE increases with the incorporation of organosilane. At a low content of organosilane, the melting point and crystallinity of the crosslinked UHMWPE increase, and hence the mechanical and wear-resisting properties are improved. However, at a high content of organosilane, these performances of the crosslinked UHMWPE become worse. At 0.4 phr silane, the wear resistance of crosslinked UHMWPE reaches its optimum value.