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用氨端基超支化聚乙烯对一种半芳香族聚酰胺进行热塑性增韧。

Thermoplastic Toughening of a Semiaromatic Polyamide with an Amino-telechelic Polyethylene.

机构信息

Ecole Polytechnique Fédérale de Lausanne (EPFL), Institute of Materials Laboratory of Macromolecular and Organic Materials, EPFL-STI-IMX-LMOM MXG 037, Station 12, 1015 Lausanne, Switzerland.

出版信息

ACS Appl Mater Interfaces. 2023 Jun 14;15(23):28430-28441. doi: 10.1021/acsami.3c00599. Epub 2023 Jun 2.

DOI:10.1021/acsami.3c00599
PMID:37264775
Abstract

Semiaromatic polyamides are used for metal replacement in advanced engineering applications to reduce weight and improve efficiency, but their range of application is limited by their inherent lack of ductility and toughness. Here, we combined semiaromatic polyamide poly(hexamethylene terephthalamide-co-isophthalamide) (PA6TI) with up to 30 wt % amine-terminated polyethylene (PE(NH)) by high-temperature melt compounding, which was suggested to lead to the formation of PA-PE block copolymers at the interface between the PE(NH) and the PA6TI. This resulted in PA6TI/PE(NH) blends with smaller, more uniform particle sizes than in PA6TI blended with nonfunctional PE or the commercial impact modifier, maleic anhydride-functionalized styrene-ethylene-butylene-styrene (SEBS) under the same conditions. The PA6TI/PE(NH) blends and the corresponding glass fiber-reinforced composites consequently showed significantly greater increases in room-temperature tensile ductility and fracture energy with respect to unmodified PA6TI, as well as maintained mechanical stability at high temperatures, and only modest decreases in stiffness and strength, even at high PE(NH) contents. These improvements were attributed to the crystallinity of the PE(NH) particles and to improved morphological stabilization and matrix-particle adhesion, consistent with the presence of PA-PE block copolymer at the matrix-particle interfaces.

摘要

半芳香族聚酰胺用于替代先进工程应用中的金属,以减轻重量和提高效率,但由于其固有的缺乏延展性和韧性,其应用范围受到限制。在这里,我们通过高温熔融共混将半芳香族聚酰胺聚(六亚甲基对苯二甲酰胺-共间苯二甲酰胺)(PA6TI)与高达 30wt%的胺封端聚乙烯(PE(NH))结合,这被认为会导致在 PE(NH)和 PA6TI 之间的界面形成 PA-PE 嵌段共聚物。这导致 PA6TI/PE(NH)共混物的粒径比在相同条件下与非功能化 PE 或商业增韧剂马来酸酐功能化苯乙烯-乙烯-丁烯-苯乙烯(SEBS)共混的 PA6TI 更小、更均匀。PA6TI/PE(NH)共混物和相应的玻璃纤维增强复合材料因此在室温拉伸延展性和断裂能方面相对于未改性的 PA6TI 显著增加,并且在高温下保持机械稳定性,即使在高含量的 PE(NH)时,刚度和强度也只有适度降低。这些改进归因于 PE(NH)颗粒的结晶度以及形态稳定性和基体-颗粒附着力的提高,这与基体-颗粒界面处存在 PA-PE 嵌段共聚物一致。

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