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Preparation and properties of biocomposites composed of glycerol-based epoxy resins, tannic acid, and wood flour

机译:由甘油基环氧树脂,鞣酸和木粉组成的生物复合材料的制备和性能

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After polyglycerol polyglycidyl ether (PGPE) and glycerol polyglycidyl ether (GPE) were mixed with tannic acid (TA) in ethanol and without solvent at epoxy/hydroxyl ratio 1/1, the obtained GPE-TA and PGPE-TA solutions were mixed with wood flour (WF), prepolymerized at 50° C, and subsequently compressed at 160°C for 3 h to give GPE-TA/WF and PGPE-TA/WF bio-composites with WF content 50-70 wt %, respectively. The storage moduli of the biocomposites in the rubbery state at more than 80°C were much higher than that of the control cured resins. The PGPE-TA/WF composites had higher tensile modulus and rather lower tensile strength than PGPE-TA. On the other hand, both the tensile modulus and strength of GPE-TA/WF were much higher than those of GPE-TA (2.4 GPa and 37 MPa). Those values of GPE-TA/WF increased with WF content, became maximal values (5.1 GPa and 51 MPa) at WF content 60 wt %, and were lowered at 70 wt %. FE-SEM analysis of the fractured surface of the biocomposites revealed that WF is tightly incorporated into the crosslinked epoxy resins. As a result of optimization of the epoxy/hydroxyl molar ratio for GPE-TA/WF composite with WF content 60 wt %, the composite prepared at the ratio of 1.0/0.8 showed the highest tensile modulus and strength.
机译:将聚甘油聚缩水甘油醚(PGPE)和甘油聚缩水甘油醚(GPE)与单宁酸(TA)在乙醇中,无溶剂的情况下以环氧/羟基比1/1混合后,将得到的GPE-TA和PGPE-TA溶液与木材混合面粉(WF),在50°C下预聚合,然后在160°C下压制3小时,分别得到WF含量为50-70 wt%的GPE-TA / WF和PGPE-TA / WF生物复合材料。在高于80℃的橡胶态下,生物复合材料的储能模量比对照固化树脂的储能模量高得多。 PGPE-TA / WF复合材料比PGPE-TA具有更高的拉伸模量和更低的拉伸强度。另一方面,GPE-TA / WF的拉伸模量和强度均远高于GPE-TA(2.4 GPa和37 MPa)。 GPE-TA / WF的那些值随WF含量增加而增加,在WF含量为60wt%时变为最大值(5.1GPa和51MPa),而在70wt%时降低。对生物复合材料断裂表面的FE-SEM分析表明,WF被紧密地结合到交联的环氧树脂中。通过优化WF含量为60wt%的GPE-TA / WF复合材料的环氧/羟基摩尔比,以1.0 / 0.8的比例制备的复合材料表现出最高的拉伸模量和强度。

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