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首页> 外文期刊>International Journal of Pharmaceutics >Poly(acrylic acid) microgels (carbopol 934)/surfactant interactions in aqueous media. Part II: Ionic surfactants.
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Poly(acrylic acid) microgels (carbopol 934)/surfactant interactions in aqueous media. Part II: Ionic surfactants.

机译:水性介质中的聚(丙烯酸)微凝胶(carbopol 934)/表面活性剂相互作用。第二部分:离子表面活性剂。

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摘要

The interaction of sodium dodecylsulfate (SDS) or benzalkonium chloride (BkCl) with carbopol microgels (0.25% (w/w)) in water was studied through pH, trasmittance, viscosity, surface tension, conductivity, fluorescence, oil solubilization, and microcalorimetry measurements. In the case of the anionic surfactant, enthalpy-driven hydrophobic absorption of SDS into carbopol microgels began when SDS concentration reached 0.05-0.08% and ended around 0.6%. These concentrations were estimated as the critical aggregation (cac) and saturation binding concentration, respectively. The hydrophobic absorption of the surfactant accompanied by its counter-ion caused carbopol microgels to swell and promoted the occurrence of bridges among several carbopol microgels. As a consequence, the consistency of the dispersions increased significantly. Above binding saturation, further addition of SDS produced a shielding effect among the anionic charges of carbopol and its dehydration, which was shown as a decrease in the viscosity of the dispersions. At low shear rates, the dispersions behaved as pseudoplastic owing to orientation of carbopol/SDS aggregates in the flow direction. Increasing shear rates caused the inter-microgel bridges to break, the water layer surrounding them to diminish, and the system to show a shear-thickening behavior. In contrast, carbopol/BkCl aggregates showed shear-thickening flow in the whole range of shear rates analyzed. Electrostatic interactions between BkCl and carbopol carboxylic groups release protons to the medium and decrease the internal osmotic pressure of the microgels. This may favor the establishment of hydrophobic interactions among surfactant tails, and induces carbopol microgels to collapse. The cac was approximately 0.01% BkCl. Saturation binding occurred at 0.3-0.5%, indicating that only 25-40mol% carboxylic groups were neutralized with BkCl. The shrinking of carbopol microgels as BkCl is absorbed prevents additional surfactant molecules from interacting with the remaining carboxylic groups. Microcalorimetry assays revealed that the aggregation process occurred with a strong gain in enthalpy.
机译:通过pH值,透光率,粘度,表面张力,电导率,荧光,油增溶和微量量热法研究了十二烷基硫酸钠(SDS)或苯扎氯铵(BkCl)与卡波姆微凝胶(0.25%(w / w))的相互作用。对于阴离子表面活性剂,当SDS浓度达到0.05-0.08%并在0.6%左右结束时,焓驱动SDS疏水吸收到Carbopol微凝胶中。这些浓度分别估计为临界聚集(cac)和饱和结合浓度。表面活性剂的疏水吸收及其抗衡离子引起卡波普微凝胶膨胀,并促进了几种卡波普微凝胶之间桥的出现。结果,分散体的稠度显着增加。在结合饱和以上,进一步添加SDS在卡波姆的阴离子电荷及其脱水之间产生屏蔽作用,这表现为分散体粘度的降低。在低剪切速率下,由于卡波姆/ SDS聚集体在流动方向上的取向,分散体表现为假塑性。剪切速率的增加导致微凝胶间桥断裂,围绕它们的水层减少,并且系统显示出剪切增稠行为。相反,在整个剪切速率范围内,carbopol / BkCl聚集体显示出剪切增稠流。 BkCl和羧甲基羧基之间的静电相互作用将质子释放到介质中,并降低了微凝胶的内部渗透压。这可能有助于在表面活性剂尾部之间建立疏水相互作用,并引起卡波普微凝胶塌陷。 CAC约为0.01%BkCl。饱和结合发生在0.3-0.5%,表明只有25-40mol%的羧基被BkCl中和。随着BkCl的吸收,卡波姆微凝胶的收缩防止了其他表面活性剂分子与其余的羧基相互作用。微量量热法测定表明,聚集过程发生时焓显着增加。

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