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Polybutadiene and styrene–butadiene rubber compounds containing a high loading of a precipitated silica nanofiller were prepared. The silica surfaces were pretreated with bis(3‐triethoxysilylpropyl) tetrasulfide to prevent the silica from interfering with the reaction mechanism of sulfur cure in the rubber. The rubber compounds were mixed together for different times and at different temperatures to produce styrene–butadiene rubber/polybutadiene rubber blends. The mass fraction and composition of the interphase in the blends were subsequently determined with modulated‐temperature differential scanning calorimetry. At 60–65°C, the mass fraction of the interphase in the blend increased after the rubbers were mixed together for 10 min, and then it decreased significantly when the mixing time was increased to 20 min. When the two rubbers were mixed together for 7 min at 60–105°C, the mass fraction of the interphase in the blend increased slightly because of a higher mixing temperature. The composition of the interphase in the blend also changed with the mixing time and mixing temperature. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
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B. Van der Bruggen 《应用聚合物科学杂志》2009,114(1):630-642
Polysulfone (PS) and poly(ether)sulfone (PES) are often used for synthesis of nanofiltration membranes, due to their chemical, thermal, and mechanical stability. The disadvantage for applying PS/PES is their high hydrophobicity, which increases membrane fouling. To optimize the performance of PS/PES nanofiltration membranes, membranes can be modified. An increase in membrane hydrophilicity is a good method to improve membrane performance. This article reviews chemical (and physicochemical) modification methods applied to increase the hydrophilicity of PS/PES nanofiltration membranes. Modification of poly(ether)sulfone membranes in view of increasing hydrophilicity can be carried out in several ways. Physical or chemical membrane modification processes after formation of the membrane create more hydrophilic surfaces. Such modification processes are (1) graft polymerization that chemically attaches hydrophilic monomers to the membrane surface; (2) plasma treatment, that introduces different functional groups to the membrane surface; and (3) physical preadsorption of hydrophilic components to the membrane surface. Surfactant modification, self‐assembly of hydrophilic nanoparticles and membrane nitrification are also such membrane modification processes. Another approach is based on modification of polymers before membrane formation. This bulk modification implies the modification of membrane materials before membrane synthesis of the incorporation of hydrophilic additives in the membrane matrix during membrane synthesis. Sulfonation, carboxylation, and nitration are such techniques. To conclude, polymer blending also results in membranes with improved surface characteristics. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
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The crystallization behavior of the blending system consists of homopolymer poly(ethylene oxide) (h‐PEO) with different molecular weights, and polystyrene‐block‐poly (ethylene oxide)‐block‐polystyrene (PS‐b‐PEO‐b‐PS) triblock copolymer has been investigated by DSC measurements. The crystallization of PEO block (b‐PEO) in block copolymer occurs under much lower temperature than that of the h‐PEO in the bulk (ΔT > 65 °C), which is attributed to the homogeneous nucleation crystallization behavior of the b‐PEO microdomains. In both the “dry‐brush” and the “wet brush” blending systems, the homogeneous nucleation crystallization temperature of PS‐b‐PEO‐b‐PS/h‐PEO blends increases due to the increase of the domain size. The heterogeneous nucleation crystallization temperatures of h‐PEO in the wet brush blending systems are higher than that of the corresponding h‐PEO in the bulk. At the same time, the heterogeneous nucleation crystallization temperature of b‐PEO10000 decreases from 43°C to 30°C and 40°C in the h‐PEO600 and h‐PEO2000 blending systems, respectively, because of the stretching of the PEO chains in the wet brush. However, this kind of phenomenon does not happen in the dry brush blending systems. The self‐seeding procedure was used to further ascertain the nucleation mechanism in the crystallization process. As a result, the self‐seeding domains have been confirmed, and the difference between the dry brush and wet brush systems has been observed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
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环氧树脂改性丙烯酸酯共聚物复合乳液的合成及性能研究 总被引:2,自引:0,他引:2
通过原位乳液聚合法和物理共混法分别制备了环氧树脂改性丙烯酸酯共聚物复合乳液,并对环氧树脂的用量和不同改性方法进行了研究。通过红外(FT-IR)、透射电镜(TEM)、力学性能测试、耐水性能测试和甲苯溶胀率测试等研究了环氧树脂改性丙烯酸酯共聚物复合乳液及乳胶膜的性能。结果表明,环氧树脂改性后的丙烯酸酯共聚物复合乳液的耐水性能、耐甲苯溶剂性能、力学性能得以提高。当物理共混法的环氧树脂用量为15%,原位乳液聚合法的环氧树脂用量为10%,得到的复合乳液和乳胶膜的综合性能较好。 相似文献