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The effects of blend ratio and storage time on thermoplastic starch/poly(butylene adipate-co-terephthalate) films

机译:混合比和储存时间对热塑性淀粉/聚己二酸丁二醇酯-对苯二甲酸对苯二甲酸酯薄膜的影响

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摘要

The objective of this work was to investigate blend ratio and storage time effects on the morphological, mechanical, and thermal properties of thermoplastic starch/poly(butylene adipate-co-terephthalate) (TPS/PBAT) films. TPS was prepared from plasticized cassava starch using a twin-screw extruder. TPS was subsequently melt-blended with PBAT with varied weight ratios (i.e., 20/80, 40/60 and 60/40) and blown to form TPS/PBAT films. It was found that increasing the TPS/PBAT ratio to 40/60 led to improved distributions of polymeric components and increased PBAT crystallization temperatures while reducing TPS melting transitions and tensile properties of TPS/PBAT films.After three months of storage at 30 °C, the tensile strength and secant modulus at 2% strain of TPS/PBAT films increased due to recrystallization of both TPS and PBAT. Blend ratios were the primary determinant for changes in TPS/PBAT film elongation at break with this storage time. Elongation at break decreased at low TPS:PBAT ratios (i.e., 20/80) and increased at high blend ratios (i.e., 60/40). The recrystallization of both TPS and PBAT components were observed from XRD and DSC analyses. Results obtained from both techniques confirmed the formation of additional crystalline structures of individual components during storage. The recrystallization phenomena also affected thermal transition temperatures of blend components. The crystallization temperature of PBAT-rich phase increased as starch could act as nucleating sites for PBAT. Using DMA, the tan δ curve of TPS/PBAT film exhibited two sharp individual peaks corresponding to the glass transitions of PBAT-rich and starch-rich phases. The tan δ of TPS-rich phase shifted to higher temperature due to recrystallization of TPS-rich phase.
机译:这项工作的目的是研究混合比例和储存时间对热塑性淀粉/聚(己二酸丁二酯-对苯二甲酸丁二醇酯)(TPS / PBAT)薄膜的形态,机械和热性能的影响。使用双螺杆挤出机由增塑的木薯淀粉制备TPS。随后将TPS与具有不同重量比(即20 / 80、40 / 60和60/40)的PBAT熔融共混并吹塑以形成TPS / PBAT膜。发现将TPS / PBAT比率提高到40/60可以改善聚合物组分的分布并提高PBAT结晶温度,同时降低TPS / PBAT膜的TPS熔融转变和拉伸性能。在30°C下保存三个月后, TPS / PBAT薄膜在2%应变下的拉伸强度和割线模量均由于TPS和PBAT的重结晶而增加。混合比是此储存时间下TPS / PBAT薄膜断裂伸长率变化的主要决定因素。在低TPS:PBAT比(即20/80)时断裂伸长率降低,而在高混合比(即60/40)时断裂伸长率提高。从XRD和DSC分析中可以观察到TPS和PBAT组分的重结晶。从这两种技术获得的结果证实了在储存过程中单个成分的其他晶体结构的形成。再结晶现象也影响了共混物组分的热转变温度。富含PBAT的相的结晶温度升高,因为淀粉可以充当PBAT的成核位点。使用DMA,TPS / PBAT膜的tanδ曲线显示出两个尖锐的独立峰,分别对应于富含PBAT和富含淀粉的相的玻璃化转变。由于富TPS相的重结晶,富TPS相的tanδ移至更高的温度。

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