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81.
82.
玻璃微珠改性PP和PE-LLD的加工流变行为 总被引:7,自引:1,他引:7
采用玻璃微珠改性两种基体性质显著不同的聚烯烃并对玻璃微珠的含量、粒径和复合材料加工方法对材料的加工流变行为进行了研究。结果表明:加工方法、玻璃微珠含量和粒径对聚丙烯/空心玻璃微珠(PP/GB)复合材料的熔体流动速率和转矩流变性能的影响远大于对PE-LLD/GB复合材料的影响,其中玻璃微珠含量的影响较粒径大。研究认为,无机刚性粒子填充改性热塑性聚合物时,加工方法、填料含量、几何特征等对复合材料流变特性是否发生影响,影响的程度等,更重要的是取决于基体树脂的特性。 相似文献
83.
84.
概述了以聚丙烯粉料部分代替传统的聚丙烯粒料来生产塑料编织袋扁丝的新工艺,分析了捏合速度、挤出温度、弓板加热温度等因素对扁丝性能的影响。 相似文献
85.
86.
β晶型成核剂改性聚丙烯纤维研究 总被引:4,自引:1,他引:4
研究了含 0 .2 5 %β晶型成核剂 (酰胺化合物 )的聚丙烯 Z3 0 S及其纤维的力学性能、晶型结构和微观形态。通过纺丝 -拉伸实验和力学性能测试、广角 X射线衍射分析、SEM观察 ,发现成核改性后生成了β晶型聚丙烯 (K值约为 75 .3 % ) ,抗冲性能大幅度提高。β晶型聚丙烯在纺丝卷绕过程中发生了β晶型→α晶型转变 ,纤维中产生约 10 %微孔隙 ,改性纤维的力学性能有所降低。 相似文献
87.
Nucleation effects of 2,2′‐methylene‐bis (4,6‐di‐tert‐butylphenyl) phosphate metal salts as a nucleating agent for isotactic polypropylene (iPP) were investigated with differential scanning calorimeter and polarized optical microscope, and their effects on mechanical, optical, and heat resistance properties of iPP were also studied. The results showed that monovalent metal salts of substituted aromatic heterocyclic phosphate such as sodium salt, lithium salt, and potassium salt had a good performance. With 0.2 wt % of sodium salt, lithium salt, or potassium salt incorporated into iPP, the crystallization peak temperature of iPP could be increased by 13.5, 13.6, and 15.0°C, respectively; the mass fraction of crystallinity of iPP could be increased by about 5%; and crystallization rate was enhanced increasingly. Meanwhile the tensile strength and flexural modulus of iPP could be increased by about 10 and 30%, respectively, and the clarity and heat distortion temperature of iPP could also be improved significantly. But bivalent and trivalent metal salts of substituted aromatic heterocyclic phosphate had little effect on properties of iPP. Meanwhile the morphology study showed that the addition of monovalent sodium salt could decrease the spherulite size of iPP significantly. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4868–4874, 2006 相似文献
88.
89.
Nucleation and crystallization of polypropylene by mineral fillers: relationship to impact strength 总被引:3,自引:0,他引:3
P.M. McGenity J.J. Hooper C.D. Paynter A.M. Riley C. Nutbeem N.J. Elton J.M. Adams 《Polymer》1992,33(24):5215-5224
The mechanical properties of mineral-filled polypropylene (PP) are determined not only by the size, shape and modulus of the filler particles, but also by microstructure. For example, poor impact strength is correlated with a high capacity for nucleation of crystallization. In the present study, optical microscopy has been used to measure the growth rate of spherulites in PP. In tandem with this, isothermal d.s.c. measurements have been made of the crystallization of the PP filled with talc, calcium carbonate and stearate-coated carbonate at different loading levels. Computer simulation of spherulite growth has been used to derive the number of nucleating sites per unit volume of polymer and, using surface area measurements, the number of sites per unit area of mineral surface was obtained. Values for talc were, as expected, considerably higher than those for carbonate (and especially coated carbonate) fillers. The presence of filler affects not only the nucleation and kinetics of the crystallization process but also the crystallinity and orientation indices and the proportion of β-phase crystallites present. The connection between these factors and impact strength is discussed. It is concluded that impact properties are determined by inter alia crack pinning and blocking by filler particles, stress concentrations at the edges of the filler particles, and the nucleating ability of the filler. 相似文献
90.
An alternative test method to the traditional 180° “T” peel test has been developed for the measurement of interlaminar bonding in three-ply (polyester/aluminium/polypropylene) flexible-packaging, laminate materials. The new test is thought to involve mixed mode I (opening) and mode II (shearing) failure, and takes into account the yielding of the polypropylene layer during testing. The method allows more direct comparisons between materials to be made, and allows the measurement of strong bonds, where a peel test would result in yield or fracture of the substrate arms before debonding. 相似文献