环氧聚氨酯与化学改性麻木芯复合材料的机械、热氧化和生物降解特性

T. Samoilenko, L. Yashchenko, N. Yarova, O. O. Leta, O. O. Brovko
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引用次数: 0

摘要

如今,天然纤维增强聚合物复合材料被认为是具有吸引力的廉价、安全和环保材料。此类复合材料的主要问题与植物纤维的亲水性有关,可以通过对其表面进行化学改性来成功解决。不过,经过这种处理后,材料的某些特性可能会受到抑制。因此,研究的目的是找出填料的化学改性对聚合物复合材料的热氧化稳定性、拉伸和弯曲强度以及生物降解性的影响。这项工作的新颖之处在于以含硅(Si)环氧聚氨酯和经化学处理的麻木芯(HWC)为基础研究新材料。麻木芯是麻类工业的副产品,需要适当加以利用。麻木芯经过氢氧化钠溶液丝光处理,再经过环氧化大豆油(ESO)或 3-氨基丙基三乙氧基硅烷(APS)进一步功能化。将未加工和表面处理过的 HWC 用作两种有机-无机环氧聚氨酯基材的增强材料,这两种基材分别由硅酸钠、基于多异氰酸酯和蓖麻油的聚氨酯预聚物以及双酚-A 二缩水甘油醚 (DGEBA) 或环氧乙烷作为环氧成分制成。对 HWC 进行官能化处理可提高复合材料的机械性能。与含有未处理填料的相应材料相比,含有 ESO 环氧聚氨酯和硅烷化 HWC 的样品的抗弯强度提高幅度最大(26%),而含有 DGEBA 环氧聚氨酯和油处理 HWC 的样品的拉伸强度提高幅度最大(53%)。使用功能化 HWC 增强的复合材料的热氧化稳定性也更高。经 APS 处理的 HWC 试样在热分解方面表现最佳。与未改性填料的复合材料相比,它们的 T50% 值高达 68 °C。同时,经 APS 或 ESO 处理的 HWC 样品最耐生物降解,这可以从它们在土壤掩埋测试中最小的重量损失中得出结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanical, thermooxidative and biodegradable properties of composites from epoxyurethanes and chemically modified hemp woody core
Natural fibre reinforced polymer composites nowadays are considered to be attractive cheap, safe and eco-friendly materials. The main problem of such composites related to the hydrophilicity of plant fibres may be successfully solved by chemical modification of their surface. However, some characteristics of the materials may be suppressed after this procedure. Therefore, the aim of the research is to find out the impact of chemical modification of filler on thermooxidative stability, tensile and flexural strength, as well as on biodegradability of polymer composites. The novelty of this work is in the examining new materials on the basis of Si-containing epoxyurethanes and chemically treated hemp woody core (HWC). Woody core that is the side product of hemp industry requiring its apropriate utilization was exposed to mercerization with sodium hydroxide solution and to further functionalization with epoxidized soybean oil (ESO) or 3-aminopropyltriethoxysilane (APS). Raw and surface treated HWC was used as reinforcement for two types of organic-inorganic epoxyurethane matrices made from sodium silicate, polyurethane prepolymer based on polyisocyanate and castor oil, and either diglycidyl ether of bisphenol-A (DGEBA) or ESO as epoxy component. Functionalization of HWC led to better mechanical properties of composites. Compared to the corresponding materials including untreated filler, maximum increase in flexural strength (26 %) was observed for the samples with ESO-containing epoxyurethane and silanized HWC, while maximum increase in tensile strength (53 %) was revealed for the ones with DGEBA-containing epoxyurethane and oil treated HWC. Thermooxidative stability was also higher for composites reinforced with functionalized HWC. The specimens with APS-treated HWC performed the best at thermal decomposition. The values of their T50% were up to 68 °C more than those for composites with unmodified filler. At the same time, the samples based on APS- or ESO-treated HWC were the most resistant to biodegradation, which may be concluded from their smallest weight loss during soil burial test.
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