A series of starch and amylose esters with different degrees of substitution and side-chain length were prepared and studied. The esters were prepared by acylation of the polysaccharide with the appropriate acid chlorides, such as octanoic, dodecanoic, and octadecanoic. The degrees of substitution were 0.54, 1.8, and 2.7. After preparation, the resulting esters were characterized by elemental analysis, 1 H nuclear magnetic resonance ( 1 H-NMR), Fourier transform infrared (FTIR), differential scanning (DSC), thermogravimetric analysis (TGA), contact angle, and water uptake measurements. Their mechanical properties and, in particular, the tensile strength and elongation at break depend on the side-chain length and on the degree of substitution. The extent of their biodegradability, after exposure to activated sludge, was assessed by weight loss measurements and scanning electron microscopy (SEM). It was found that these new materials are biodegradable, and the biodegradation rate decreases with increasing degree of esterification.
A series of LDPE blends with plasticized (PLST) and granular starch (FILST) were prepared. Ethylene/vinyl acetate (EVA) copolymer was used as a compatibilizer in three different amounts: 10.25 and 50 wtYo based on starch. The blends were studied by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetric analysis 0. Second derivative IR spectra showed peak shifts similar to those observed in V-type starch complexes with ethylene/vinyl alcohol copolymers. The possibility for V-type complex formation is supported by the lower biodegradation rates of the blends containing higher amounts of EVA. Mechanical properties of the blends, especially elongation at break, were satisfactory even for blends containing high amounts of starch (2&30 wt?!).
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