Rotureau E, Leonard M, Dellacherie E, Durand A
Laboratoire de Chimie Physique Macromoléculaire, UMR CNRS-INPL 7568, Groupe ENSIC, BP 451, 54001 Nancy Cedex, France.
J Colloid Interface Sci. 2004 Nov 1;279(1):68-77. doi: 10.1016/j.jcis.2004.06.040.
Ionic amphiphilic dextran derivatives were synthesized by the attachment of sodium sulfopropyl and phenoxy groups on the native polysaccharide. A family of dextran derivatives was thus obtained with varying hydrophobic content and charge density in the polymer chains. The surface-active properties of polymers were studied at the air-water and dodecane-water interfaces using dynamic surface/interfacial tension measurements. The adsorption was shown to begin in a diffusion-limited regime at low polymer concentrations, that is to say, with the diffusion of macromolecules in the bulk solution. In contrast, at long times the interfacial adsorption is limited by interfacial phenomena: adsorption kinetics or transfer into the adsorbed layer. A semiempirical equation developed by Filippov was shown to correctly fit the experimental curves over the whole time range. The presence of ionic groups in the chains strongly lowers the adsorption kinetics. This effect can be interpreted by electrostatic interactions between the free molecules and the already adsorbed ones. The adsorption kinetics at air-water and oil-water interfaces are compared.
通过将磺丙基钠和苯氧基连接到天然多糖上,合成了离子型两亲性葡聚糖衍生物。由此获得了一系列聚合物链中疏水含量和电荷密度不同的葡聚糖衍生物。使用动态表面/界面张力测量法研究了聚合物在空气-水和十二烷-水界面的表面活性性质。结果表明,在低聚合物浓度下,吸附开始于扩散限制区域,也就是说,大分子在本体溶液中扩散。相反,在较长时间内,界面吸附受界面现象限制:吸附动力学或转移到吸附层中。结果表明,Filippov 提出的半经验方程在整个时间范围内能正确拟合实验曲线。链中离子基团的存在极大地降低了吸附动力学。这种效应可以通过自由分子与已吸附分子之间的静电相互作用来解释。比较了空气-水和油-水界面的吸附动力学。