LLDPE/LLDPE-g-AA共混物的接触角及红外光谱表征

利用熔融共混的方法制备了线性低密度聚乙烯/线性低密度聚乙烯接枝丙烯酸(LLDPE/LLDPE-g-AA)共混物。用傅里叶红外光谱(FT-IR)和测定接触角的方法对不同LLDPE-g-AA含量的LLDPE/LLDPE-g-AA共混物膜的表面进行了表征。结果表明,随着共混物中LLDPE-g- AA含量的增加,水和甘油等极性液体与共混物表面的接触角下降。依据共混物的FT-IR计算了其羧基峰强度。发现极性液体与LLDPE/LLDPE-g- AA共混物膜表面的接触角越小,羧基峰强度越大。

PA46/PP-g-GMA合金的研制和表征

用反应挤出方法制备了PA46/PP-g-GMA合金。研究了合金的力学性能,吸水性与形态结构的关系。与PA46/PP相比,PA46/PP-g- GMA的力学性能如拉伸强度,杨氏模量,弯曲强度,弯曲模量以及冲击强度都有不同程度的提高。PA46/PP-g-GMA的吸水率比PS46/PP大幅度降低。用扫描电镜(SEM)研究了PA46/PP-g-GMA和PA46/PP样品的冲击断面。PA46/PP-g-GMA中的PP-g-GMA分散相粒子半径远比PA46/PP中的PP相粒子半径小和均匀。这表明改性后的PP-g-GMA与PA46的相容性有很大的改观。DMA研究结果表明,PA46 /PP-g-GMA样品的储能模量比相同组分的PP/PA46高。在组成为50/50时PA46/PP-g-GMA的软化点温度比PA46/PP高 120℃。

Morphologies and physical properties of PA1010/HIPS/HIPS-g-MA ternary blends

The effect of the content of a copolymer consisting of high impact polystyrene grafted with maleic anhydride (HIPS-g-MA) on morphological and mechanical properties of PA1010/HIPS blends has been studied. Blend morphologies were controlled by adding HIPS-g-MA during melt processing, thus the dispersion of the HIPS phase and interfacial adhesion between the domains and matrices in these blends were changed obviously. The weight fractions of HIPS-g-MA in the blends increased from 2.5 to 20, then much finer dispersions of discrete HIPS phase with average domain sizes decreased from 6.1 to 0.1 mu m were obtained. It was found that a compatibilizer, a graft copolymer of HIPS-g-MA and PA1010 was synthesized in situ during the melt mixing of the blends. The mechanical properties of compatibilized blends were obviously better than those of uncompatibilized PA1010/HIPS blends. These behaviors could be attributed to the chemical interactions between the two components of PA1010 and HIPS-g-MA and good dispersion in PA1010/HIPS/HIPS-g-MA blends. Evidence of reactions in the blends was seen in the morphology and mechanical behaviour of the solid. The blend containing 5 wt % HIPS-g-MA component exhibited outstanding toughness. (C) 1999 Kluwer Academic Publishers.

Compatibilization effect of graft copolymer on immiscible polymer blends: 1. LLDPE/SBS/LLDPE-g-PS systems

compatibilizing effect of graft copolymer, linear low density polyethylene-g-polystyrene (LLDPE-g-PS), on immiscible blends of LLDPE with styrene-butadiene-styrene triblock copolymer (SBS) has been investigated by means of C-13 CPMAS n.m.r. and d.s.c. techniques. The results indicate that LLDPE-g-PS is an effective compatibilizer for LLDPE/SBS blends. It was found that LLDPE-g-PS chains connect two immiscible components, LLDPE and SBS, through solubilization of chemically identical segments of LLDPE-g-PS into the amorphous region of LLDPE acid PS block domain of SBS, respectively. It was also found that LLDPE-g-PS chains connect the crystalline region of LLDPE by isomorphism, with serious effects on the supermolecular structure of LLDPE. The effect of LLDPE-g-PS on the supermolecular structure of LLDPE in the LLDPE/SBS blends obviously depends on the composition of the blends, but has little dependence on the PS grafting yields of LLDPE-g-PS. (C) 1998 Elsevier Science Ltd. All rights reserved.

Effects of the compatibilizer PP-g-GMA on morphology and mechanical properties of PP/PC blends

Effects of the compatibilizer polypropylene grafted with glycidyl methacrylate(PP-g-GMA) on the morphology, thermal, rheological and mechanical properties of polypropylene and polycarbonate blends (PP/PC) were studied. It was found that the addition of PP-g-GMA significantly changed their morphology. The mean size of domains reduced from 20 mu m to less than 5 mu m. The dispersed domain size is also strongly dependent upon the content of PP-g-GMA. The interfacial tension of PP/PC/PP-g-GMA (50/30/20) is only about one-tenth of PP/PC (70/30). The crystallization temperature of PP in PP/PC/PP-g-GMA is 5-8 degrees C higher than that of PP in PP/PC blends. Characterization studies based on mechanical properties, differential scanning calorimetry, rheology and morphological evidence obtained by using scanning electron microscopy support the hypothesis that an in-situ copolymer PP-g-PC was formed during the blending process. (C) 1997 Elsevier Science Ltd.

Morphology, mechanical properties and interfacial behaviour of PA1010/PP/PP-g-GMA ternary blends

Morphology, mechanical properties, and interfacial interaction of polyamide 1010/polypropylene (PA1010/ PP) blends compatibilized with polypropylene grafted with glycidyl methacrylate (PP-g-GMA) were studied. It was found that the size of the PP domains, tensile and impact strength of ternary blends, and adhesion fracture energy between two layers of PA1010 and PP were all significantly dependent on the PP-g-GMA contents in the PP layer. Correlations between morphology and related properties were sought. The improvements in properties have been attributed to chemical and physical interaction occurring between PA1010 and PP-g-GMA. (C) 1997 Elsevier Science Ltd.

Morphology, thermal behavior, and mechanical properties of PA1010/PP and PA1010/PP-g-GMA blends

The modification of polypropylene (PP) was accomplished by melt grafting glycidyl methacrylate (GMA) on its molecular chains. The resulting PP-g-GMA was used to prepare binary blends of polyamide 1010 (PA1010) and PP-g-GMA. Different blend morphologies were observed by scanning electron microscopy (SEM) according to the nature and content of PA1010 used. Comparing the PA1010/PP-g-GMA and PA1010/PP binary blends, the size of the domains of PP-g-GMA were much smaller than that of PP at the same compositions. It was found that mechanical properties of PA1010/PP-g-GMA blends were obviously better than that of PA1010/PP blends, and the mechanical properties were significantly influenced by wetting conditions for uncompatibilized and compatibilized blends. A different dependence of the flexural modulus on water was found for PA1010/PP and PA1010/PP-g-GMA. These behaviors could be attributed to the chemical interactions between the two components and good dispersion in PA1010/PP-g-GMA blends. Thermal and rheological analyses were performed to confirm the possible chemical reactions taking place during the blending process. (C) 1997 John Wiley & Sons, Inc.

Isothermal crystallization of PP-g-GMA copolymer

The overall isothermal crystallization kinetics for neat polypropylene and grafted polypropylene systems were investigated. The rate constants were corrected assuming the heterogeneous nucleation and three dimensional growth of polypropylene spherulites. A semiempirical equation for the radial growth rate of polypropylene spherulites was developed as a function of temperature, and was used to determine the number of effective nuclei of different temperatures. The number of nuclei in grafted samples was estimated to be 10(2)-10(3) times larger than that of neat polypropylene. (C) 1997 John Wiley & Sons, Inc.

Interaction characterization of PA1010/PP blends using PP-g-AA as compatibilizer

The morphology of polyamidelOlO/polypropylene blends was found to significantly depend upon the concentration of the compatibilizer[polypropylene-grafted-acrylic acid (PP-g-AA)]. A significant reduction in phase size was observed because of the interaction that existed between the PP-g-AA and polyamide. These interactions have been confirmed by several methods. The tensile mechanical properties and impact behavior of the prepared blends were investigated and correlated with scanning electron microscope (SEM) analysis of the fracture surfaces. It was found that PP-g-AA as the compatibilizer has a profound effect upon the properties of the blends. This behavior is attributed to a series of chemical and physico-chemical interactions taking place between the two components.

The chemistry of alpha-oxo ketene cyclic dithioacetal .36. Studies on silica G catalyzed decomposition of adducts of beta,beta-1,3-propylenedithio-alpha,beta-unsaturated arylketones with grignard reagents

beta, beta-1, 3-Piopylenedithio-alpha, beta-unsaturated arylketones 2 via chemoselective 1,2-addition with allyl or benzyl Grignard reagents afforded the corresponding carbinols 3 and 4. Catalysed by silica gel, the carbinols 3 and 4 were converted to the beta,gamma-unsaturated arylketones 5, 6. The mechanism and reaction condition were discussed.

Compatibilization effect of graft copolymer on immiscible polymer blends .2. LLDPE/PS/LLDPE-g-PS systems

The compatibilizing effect of graft copolymer, linear low density polyethylene-g-polystyrene (LLDPE-g-PS), on immiscible LLDPE/PS blends has been studied by means of C-13 CP-MAS NMR and DSC techniques. The results indicate that LLDPE-g-PS is an effective compatibilizer for LLDPE/PS blends, and the compatibilizing effect of LLDPE-g-PS on LLDPE/PS blends depends on the PS grafting yield and molecular structure of the compatibilizers and also on the composition of the blends. It was found that LLDPE-g-PS chains connect two immiscible components, LLDPE and PS, through solubilization of chemically identical segments of LLDPE-g-PS into the noncrystalline region of the LLDPE and PS domain, respectively. Meanwhile, LLDPE-g-PS chains connect the crystalline region of LLDPE by isomorphism, resulting in an obvious change in the crystallization behavior of LLDPE. (C) 1996 John Wiley & Sons, Inc.

PP－g－AA的制备和表征

用熔融接枝方法制备了聚丙烯－ｇ－丙烯酸（ＰＰ－ｇ－ＡＡ）。用光电子能谱，广角Ｘ射线衍射，红外光谱和化学滴定方法对接枝物进行了定性和定量表征。讨论了单体和引发剂浓度对接枝率的影响，确定了用红外光谱法测定接枝物含量的经验公式

PP－g－PMMA在PP／PVDF共混体系中的应用

利用聚丙烯等离子体接枝甲基丙烯酸甲酯共聚物（ＰＰ－ｇ－ＰＭＭＡ）作增容剂，研究了其在聚丙烯／聚偏氟乙烯（ＰＶＤＦ）共混体系中的作用。增容是通过ＰＭＭＡ与ＰＶＤＦ的偶极－偶极相互作用实现的。接枝共聚物使共混体系的抗张强度和模量均有提高，由不同等离子体处理时间所得的ＰＰ－ｇ－ＰＭＭＡ，接枝率在７．７％～３００％具有最好的增容效果；而由不同后聚合时间所得的共聚物，接枝率在３０％～８０％具有最好的增容效果。

EP－g－GMA热学行为表征

本文用ＤＳＣ研究了乙丙共聚物接枝甲基丙烯酸环氧丙酯（ＥＰ－ｇ－ＧＭＡ）的热学性质。与空白乙丙共聚物相比，接枝共聚物中丙烯序列的结晶温度升高了８～１２℃，熔融热焓增加了４～６Ｊ／ｇ。乙烯序列的结晶温度却稍有下降，其相应熔点及熔融热熔都有相应下降。等温与非等温结晶动力学表明接枝样品中丙烯序列的结晶速率高于相应的未接枝样品，ＥＰ－ｇ－ＧＭＡ的Ａｖｒａｍｉ指数及Ｚｉａｂｉｃｋｉ指数均高于空白ＥＰ，接枝到乙丙共聚物乙烯序列上的甲基丙烯酸环氧雨酯（ＧＭＡ）可能成为丙烯序列结晶的成核剂，加速了丙烯的成核速度和晶体增长速度。

PA6/SBS-g-MAH共混物的形态与力学性能

利用扫描电子显微镜、偏光显微镜对尼龙6/马来酸酐接枝SBS共混物的形态结构进行了研究,对其力学性能、吸水率进行了测试和表征。结果表明,用马来酸酐接枝的SBS与尼龙6有较好的相容性,其室温和低温下的缺口冲击强度比纯尼龙6有大幅度提高,吸水率有所降低。