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用U形管电泳仪在电压为30V条件下测定了造纸用羧基丁苯胶乳(牌号XSBRL46C)的ξ电位;研究了十二烷基硫酸钠(SDS)、十二烷基苯磺酸钠(SDBS)、电解质溶液的浓度及pH值对ξ电位及稳定性的影响。结果表明:SDS和SDBS的浓度超过临界胶束浓度后,ξ电位增值减小;当乳液pH值小于7或大于9时,ξ电位减小,乳液稳定性降低。 相似文献
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用电导滴定法和红外光谱分析法对三种羧基丁苯胶胶的羧基分布进行了研究。并且根据所得结果对胶乳的稳定性进行了分析。 相似文献
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A dielectric self-crosslinking hydrogenated carboxylated nitrile butadiene rubber (HXNBR) latex film was prepared by diimide reduction hydrogenation of XNBR latex and the doping of multi-walled carbon nanotube (MWCNT). The structures of the HXNBR and XNBR were characterised by Fourier transform infrared spectroscopy (FTIR) and 1HNMR, confirming the successful hydrogenation of XNBR. The mechanical, thermal, and electrical properties of the prepared HXNBR latex films were studied, and the HXNBR latex film reinforced by only 3?phr MWCNTs exhibited improved mechanical, thermal, and dielectric properties. 相似文献
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Ranimol Stephen A. M. Siddique Fouran Singh Lekshmi Kailas Seno Jose Kuruvilla Joseph Sabu Thomas 《应用聚合物科学杂志》2007,105(2):341-351
The effect of microfillers on the thermal stability of natural rubber (NR), carboxylated styrene butadiene rubber (XSBR) latices, and their 70/30 NR/XSBR blend were studied using thermogravimetric method. Microcomposites of XSBR and their blend were found to be thermally more stable than unfilled samples. The activation energy needed for the degradation of polymer chain was calculated from Coats‐Redfern plot. Activation energy needed for the thermal degradation of filled samples was higher than unfilled system. It indicated the improved thermal stability of the filled samples. The ageing resistance of the micro‐filled samples was evaluated from the mechanical properties of aged samples. The thermal ageing was carried out by keeping the samples in hot air oven for 7 days at 70°C. The mechanical properties such as tensile strength, modulus at 300% elongation, and strain at break were computed. As compared to unfilled samples, micron‐sized fillers reinforced systems exhibited higher ageing resistance. Finally, an investigation was made on the influence of ion‐beam irradiation on microcomposites of NR, XSBR latices, and their 70/30 blend systems using 28Si8+ performed at 100 MeV. The surface changes of the samples after irradiation were analyzed using X‐ray photoelectron spectroscopy. The results of XPS measurements revealed that the host elements were redistributed without any change in binding energies of C1s, O1s, and Si2p. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 相似文献
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以过硫酸铵为引发剂,十二烷基硫酸钠为乳化剂,采用种子聚合工艺,合成了偏氯乙烯质量分数为23%~43%的羧基偏氯乙烯丁苯胶乳。通过电镜观察到所合成的胶乳粒子具有核-壳结构。通过测定胶闰子表面层的羧基数量,研究了羧基的分布,结果表明,羧酸种类对羧基在胶乳粒子中及在聚合体系中的分布有重要影响,该胶乳作为地毯背衬粘合剂,具有粘合力高,极限氧指数高的特点,是一种较好的阻燃性粘合剂。 相似文献
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This article focuses mainly on the effect of maturation time on the rheological behavior of unvulcanized natural rubber (NR)–styrene butadiene rubber (SBR) latex blends. Viscosity shows a composition-dependent behavior with maturation time. It was found that there is a marginal decrease in viscosity for all the systems with maturation time except for the 70/30 NR–SBR blend. In this blend, there is a sharp decrease in viscosity with maturation time. This is associated with the exchange of stabilizers with one another until an equilibrium is reached; that is, all the particles of the blend are stabilized with random mixture of stabilizers. The structural build up observed in 70/30 NR–SBR blend was found to be diminished as the maturation time increases. At equilibrium, there is no further exchange of stabilizers. The behavior of this blend has been explained with the help of a schematic model. The effects of blend ratio and surface active agents on the viscosity were also studied. In addition, the time-dependent flow behavior of prevulcanized latex blends was evaluated as a function of vulcanizing systems and prevulcanization time. There is a regular increase in viscosity with prevulcanization time. However, after 3 h, the viscosity of almost all blends levels off, indicating that the curing reaction is complete within this time. Finally, the morphological changes occurred during film formation of the blends were studied using scanning electron microscopy. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 1473–1483, 1998 相似文献
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