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Structure and Properties of Polymer-Polymer Composites Based on Biopolymers and Ultra-High Molecular Weight Polyethylene Obtained via Ethylene In Situ Polymerization

机译:乙烯原位聚合获得的基于生物聚合物和超高分子量聚乙烯的聚合物-聚合物复合材料的结构和性能

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摘要

Polymer-polymer composites (PPC) of biopolymers (starch, cellulose, poly-3-hydroxybutyrate) and ultra-high molecular weight polyethylene (UHMWPE) were obtained by ethylene in situ polymerization (polymerization filling). Ethylene polymerization was carried out in "mild" conditions (25 A degrees C, 0.1 MPa) on a traditional Ziegler-Natta catalyst [TiCl4 + (C2H5)(2)AlCl], biopolymer-supported. Catalyst activity increases in the presence of polysaccharides depending on their type and quantity. UHMWPE matrix possesses a molecular weight of 1.20-1.65 MDa, melting point of 138-143 A degrees C, high melting enthalpy and a crystallinity of 60-70%. PPCs generally exhibit better tensile properties than neat polyethylene, such as elastic modulus and elongation at break. Thermogravimetric analysis shows a significant decrease in decomposition temperature and the rate of mass loss on both stages of PPC destruction. The photo-oxidative destruction of PPC after UV-irradiation for different periods of time was studied by FTIR and XRD. Carbonyl indices indicate the rate of oxidation to be 3-4 times greater than in neat PE. Prolonged irradiation leads to a considerable increase in crystallinity and crystallite size. Irradiated PPC films show a 90% extent of biofouling by mold fungi, compared to no growth apparent for neat samples.
机译:通过乙烯原位聚合(聚合填充)获得生物聚合物(淀粉,纤维素,聚-3-羟基丁酸酯)和超高分子量聚乙烯(UHMWPE)的聚合物-聚合物复合材料(PPC)。乙烯聚合是在传统的Ziegler-Natta催化剂[TiCl4 +(C2H5)(2)AlCl]上,在“温和”的条件下(25 A摄氏度,0.1 MPa)进行的,该催化剂由生物聚合物负载。在多糖存在下,取决于其类型和数量,催化剂活性会增加。 UHMWPE基质的分子量为1.20-1.65 MDa,熔点为138-143 A摄氏度,熔融焓高,结晶度为60-70%。 PPC通常表现出比纯聚乙烯更好的拉伸性能,例如弹性模量和断裂伸长率。热重分析表明,在分解PPC的两个阶段中,分解温度和质量损失率均显着降低。通过FTIR和XRD研究了紫外线辐照不同时间后PPC的光氧化破坏。羰基指数表明氧化速率是纯PE的3-4倍。长时间的照射导致结晶度和微晶尺寸的显着增加。辐照的PPC薄膜显示出90%的霉菌对生物的污染,而纯净样品则没有明显的增长。

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