石墨烯衍生物/热塑性淀粉复合材料的物理和生物降解性能

W. H. Ferreira, C. T. Andrade
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引用次数: 2

摘要

开发可生物降解的包装材料是一个非常重要的问题。这些材料是石油基聚合物的替代品,石油基聚合物在处理后会造成环境污染。在这项工作中,氧化石墨烯(GO)和葡萄糖还原氧化石墨烯(rGO-g)通过熔融挤出掺入热塑性淀粉(TPS)。比较了TPS/GO和TPS/rGO-g复合材料的物理性能和生物降解性。x射线衍射(XRD)结果表明,石墨烯的种类导致了石墨烯片的分散程度不同,并导致了TPS晶体结构的变化。压缩成型复合材料的拉伸试验表明,TPS/rGO-g复合材料具有较好的力学性能。当rGO-g添加量为1.0和2.0质量%时,TPS的杨氏模量(E)分别从E =(28.6±2.7)MPa增加到E =(110.6±9.5)MPa和E =(144.2±11.2)MPa。石墨烯衍生物中的酸基促进了淀粉分子的糖苷键断裂,并改善了复合材料的生物降解。氧化石墨烯在TPS基质中分散良好,有助于生物降解。对于TPS/rGO-g材料,rGO-g分散水平影响其生物降解。
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Physical and Biodegradation Properties of Graphene Derivatives/Thermoplastic Starch Composites
Development of biodegradable materials for packaging is an issue of the utmost importance. These materials are an alternative to petroleum-based polymers, which contribute to environment pollution after disposal. In this work, graphene oxide (GO) and glucose-reduced graphene oxide (rGO-g) were incorporated to thermoplastic starch (TPS) by melt extrusion. The TPS/GO and TPS/rGO-g composites had their physical properties and biodegradability compared. X-ray diffraction (XRD) showed that the type of graphene used led to different dispersion levels of graphene sheets, and to changes in the crystalline structure of TPS. Tensile tests carried out for the compression-molded composites indicated that TPS/rGO-g composites presented better mechanical performance. The Young’s modulus (E) increased from E = (28.6 ± 2.7) MPa, for TPS, to E = (110.6 ± 9.5) MPa and to (144.2 ± 11.2) MPa for TPS with rGO-g incorporated at 1.0 and 2.0 mass% content, respectively. The acid groups from graphene derivatives promoted glycosidic bond breakage of starch molecules and improved biodegradation of the composites. GO is well-dispersed in the TPS matrix, which contributes to biodegradation. For TPS/rGO-g materials, biodegradation was influenced by rGO-g dispersion level.
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