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Competitive plasticization in ternary plasticized starch biopolymer system

机译:三元增塑淀粉生物聚合物体系中的竞争增塑

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摘要

Two plasticizers namely, glycerol and xylitol, based on their similar molecular diameter (~ 6.3 ?) but different molecular weights (glycerol-92; xylitol-152) were selected were selected for studying the plasticization of starch biopolymer containing 70% amylopectin structure via glass transition measurements carried over a wide range of water activity. A standard calorimetry was used to determine the onset temperature of polymeric viscous flow. For both glycerol and xylitol, typical antiplasticization was evident at low plasticizer concentrations, whereas at higher concentration, there was significant reduction in glass transition temperature. Water activity isotherms showed that equilibrium moisture content of the starchbiopolymer (no plasticizer) steadily increases up to 11%, however, for plasticized biopolymer, the moisture content was nearly double than that of biopolymer. We used a modified Gordon-Taylor model, using a new interaction parameter, to understand the competitive plasticization of glycerol and xylitol in presence of water, and determined 8 wt % water as a threshold amount of matrix water for strong three-way interactions: starch-plasticizer, plasticizerplasticizer/water and starch-water.
机译:根据其相似的分子直径(〜6.3?)但分子量不同(甘油-92;木糖醇-152),选择了两种增塑剂甘油和木糖醇,通过玻璃研究含70%支链淀粉结构的淀粉生物聚合物的增塑作用。过渡测量涵盖了广泛的水活度。使用标准量热法确定聚合物粘性流的起始温度。对于甘油和木糖醇,在低增塑剂浓度下,典型的抗塑化作用明显,而在高浓度下,玻璃化转变温度显着降低。水分活度等温线表明,淀粉生物聚合物(无增塑剂)的平衡含水量稳定增加至11%,但是,对于增塑的生物聚合物,含水量几乎是生物聚合物的两倍。我们使用改良的Gordon-Taylor模型(使用新的相互作用参数)来了解在水存在下甘油和木糖醇的竞争性增塑作用,并确定了8 wt%的水作为用于强三效相互作用的基质水的阈值量:淀粉-增塑剂,增塑剂/增塑剂/水和淀粉-水。

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