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Flax Fiber Reinforced Arylated Soy Protein Isolate

机译:亚麻纤维增强芳基化大豆蛋白分离物

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Soy protein plastics prepared by solution casting method can achieve the modulus of 20-50 MPa while that of soy protein plastics prepared by compression molding ranges from 50-100 MPa at high relative humidity (50 to 75% RH). On the other hand, modulus of natural fiber bundle varies between 650 and 1050 MPa. So the modulus of soy protein based plastics is relatively very less compared to that of natural fibers. It has been recently reported that arylation of soy protein in presence of 2,2-diphenyl-2-hydroxyethanoic acid (DPHEAc) leads to protein material with very high modulus in the range of 800 to 1100 MPa even at high relative humidity (50 to 75% RH). Water-mediated arylation by dip coating method is responsible for the high modulus of soy protein materials. Here, we are reporting damage-sensitive composites prepared from arylated soy protein (as brittle-matrix) and flax fabric. Bio-composites were successfully prepared by reinforcing soy protein isolate with different weight fractions (0.2 to 0.4) of woven flax fabric. Flax fabric reinforced soy protein isolate based composites were then arylated with 2, 2-diphenyl-2-hydroxyethanoic acid (DPHEAc) for 4 h to get arylated bio-composites. Characterizations of the arylated and non-arylated bio-composites were performed by thermo gravimetric analysis. Results indicated that arylated soy protein based composites displayed mechanical behaviour like brittle-matrix composites that differentiated them from non-arylated soy protein based composites which displayed mechanical behaviour like polymermatrix composites. Scanning electron microscopy was also carried out to understand the nature of cracks and fractures suffered by the arylated soy protein composites when subjected to tensile tests.
机译:通过溶液铸造方法制备的大豆蛋白塑料可以实现20-50MPa的模量,而通过压缩成型的大豆蛋白塑料的模量在高相对湿度(50至75%RH)下的50-100MPa。另一方面,天然纤维束的模量在650和1050MPa之间变化。因此,与天然纤维相比,大豆基蛋白基塑料的模量相对较少。最近据报道,在2,2-二苯基-2-羟基乙酸(DPHEAC)存在下大豆蛋白的浓缩,导致蛋白质材料,即使在高相对湿度(50至50)的情况下,蛋白质材料在800-1100MPa的范围内75%RH)。通过浸涂方法进行水介导的芳基化对大豆蛋白材料的高模量负责。在此,我们报告由芳族化大豆蛋白(作为脆性基质)和亚麻织物制备的损伤敏感复合材料。通过用不同重量级分(0.2至0.4)编织亚麻织物的大豆蛋白分离物成功地制备生物复合材料。然后将亚麻织物增强大豆分离物的复合材料用2,2-二苯基-2-羟乙基甲酸(DPHEAC)占据芳基4小时以获得芳族化生物复合材料。通过热重量分析进行芳基化和非芳基化生物复合材料的特征。结果表明,诸如脆性基质复合材料等芳基的大豆基复合材料如脆性 - 基质复合材料,从非芳族化大豆蛋白基复合材料区分化,其如PolyMatrix复合材料等机械行为。还进行了扫描电子显微镜,以了解在经受拉伸试验时由芳齐的大豆蛋白复合材料所患者所患者的裂缝和裂缝的性质。

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