Mechanical properties improvement of thermoplastic corn starch and polyethylene-grafted-maleicanhydride blending by Na+ ions neutralization of carboxymethyl cellulose.

Corn starch was melt-blended with glycerol (70/30) to prepare thermoplastic starch (TPS) at 140 °C for 10 min. The TPS was melt-blended with polyethylene grafted with maleic anhydride (PE-MAH) and carboxymethyl cellulose (CMC) to improve the properties of the TPS. Phase determination analysis and SEM images demonstrated that the morphology of the TPS/PE-MAH/CMC blend consisted of PE-MAH particles dispersed in the TPS matrix. The tensile strength and elongation were found to have improved with the addition of CMC 5 wt%. Adhesion between the polymers was observed by the asymmetric double-cantilever beam (ADCB) method. The PE-MAH/(TPS + CMC) sample showed high fracture toughness (Gc), which is related to the adhesion energy between the two polymers. This is suggestive of interactions between the MAH groups of PE-MAH and CMC. FT-IR results indicated that the neutralization and aggregation were formed by Na+ ions of CMC and the MAH of PE-MAH, which increased the interfacial adhesion between TPS and PE-MAH blend. The improvement in the mechanical properties of the TPS/PE-MAH/CMC blend is concluded to be because of the increase in the interfacial adhesion between TPS and PE-MAH by these neutralization and aggregation processes.

Reactive blending of thermoplastic starch and polyethylene-graft-maleic anhydride with chitosan as compatibilizer.

Cassava starch was melt-blended with glycerol (70/30wt%/wt%) at 140°C to prepare thermoplastic starch (TPS). Chitosan (CTS) was premixed with starch and glycerol, in acidified water (lactic acid 2wt%), at 1, 5 and 10wt%/wt%. TPS/CTS was then melt-blended (160°C) with polyethylene-graft-maleic anhydride (PE-MAH). Phase determination and scanning electron microscopy indicated TPS/PE-MAH/CTS had a co-continuous morphology and CTS-induced phase inversion to give dispersed PE-MAH particles in a TPS matrix. Tensile strength at break and elongation, melt viscosity, fracture toughness and water contact angle of TPS/PE-MAH were improved by CTS incorporation. TPS/PE-MAH/CTS blends decreased the melting temperature of TPS and PE-MAH compared to the neat polymers. FTIR confirmed a reaction had occurred between amino groups (NH2) of CTS and the MAH groups of PE-MAH. This reaction and the enhanced miscibility between TPS and CTS improved the mechanical properties of the TPS/PE-MAH/CTS blend, particularly at 5wt%/wt% CTS.