Department of Inorganic, Analytical, and Applied Chemistry, University of Geneva, Sciences II, 30, Quai Ernest-Ansermet, 1211 Geneva 4, Switzerland.
J Phys Chem B. 2010 Mar 11;114(9):3170-7. doi: 10.1021/jp911482a.
The interaction forces between individual positively charged amidine functionalized latex particles with adsorbed negatively charged sodium poly(styrene sulfonate) were studied with the colloidal probe technique based on atomic force microscopy (AFM). When the polymer dose is progressively increased, the strength of the repulsive force between the particles decreases as the charge neutralization point is approached, then increases again due to overcharging, and finally reaches a plateau. Surface potentials obtained from fits of the force profiles to Poisson-Boltzmann theory agree well with potentials measured with electrophoresis. Close to the charge neutralization point, attractive forces exceeding van der Waals interactions are found. These attractive forces increase in strength with increasing molecular mass of the polymer and decreasing ionic strength. These attractive interactions are of electrostatic origin and result from lateral patch-charge heterogeneities within the adsorbed polyelectrolyte layer. The measured forces are shown to be in semiquantitative agreement with model calculations based on charge distributions with square lattice symmetry.
采用基于原子力显微镜(AFM)的胶体探针技术研究了带有吸附的负电荷的聚(苯乙烯磺酸钠)的带正电的脒基功能化胶乳颗粒之间的相互作用力。当聚合物剂量逐渐增加时,当接近电荷中和点时,颗粒之间的排斥力强度减小,然后由于过充电再次增加,最后达到一个平台。从力曲线拟合到泊松-玻尔兹曼理论中获得的表面电势与电泳测量的电势吻合得很好。在接近电荷中和点的位置,发现了超过范德华相互作用的吸引力。这些吸引力随着聚合物的分子量增加和离子强度降低而增强。这些吸引力是静电起源的,是由吸附的聚电解质层中的横向位错电荷不均匀性引起的。所测量的力与基于具有正方形晶格对称性的电荷分布的模型计算具有半定量一致性。