Adamczyk Z, Zembala M, Michna A
Institute of Catalysis and Surface Chemistry, Polish Academy of Science, Niezapominajek 8, 30-239 Cracow, Poland.
J Colloid Interface Sci. 2006 Nov 15;303(2):353-64. doi: 10.1016/j.jcis.2006.07.083. Epub 2006 Sep 1.
Adsorption of a cationic polyelectrolyte, polyallylamine hydrochloride (PAH), having a molecular weight of 70,000 on mica was characterized by the streaming potential method and by deposition of negative polystyrene latex particles. Formation of PAH layers was followed by determining the apparent zeta potential of surface zeta as function of bulk PAH concentration. The zeta potential was calculated from the streaming potential measured in the parallel-plate channel formed by two mica plates precovered by the polyelectrolyte. The experimental data were expressed as the dependence of the reduced zeta potential zeta/zeta0 on the PAH coverage Theta(PAH), calculated using the convective diffusion theory. It was found that for the ionic strength of 10(-2) M, the dependence of zeta/zeta0 on Theta(PAH) can be reflected by the theoretical model formulated previously for surfaces covered by colloid particles. The electrokinetic measurements were complemented by particle deposition experiments on PAH-covered mica surfaces. A direct correlation between the polymer coverage and the initial deposition rate of particles, as well as the jamming coverage, was found. For ThetaPAH > 0.3 the initial deposition rate attained the value predicted from the convective diffusion theory for homogeneous surfaces. The initial deposition rates for surfaces modified by PAH were compared with previous experimental and theoretical results obtained for heterogeneous surfaces formed by preadsorption of colloid particles. It was revealed that negative latex deposition occurred at surfaces exhibiting negative apparent zeta potential, which explained the anomalous deposition of particles observed in previous works. It was suggested that the combined electrokinetic and particle deposition methods can be used for detecting adsorbed polyelectrolytes at surfaces for coverage range of a percent. This enables one to measure bulk polyelectrolyte concentrations at the level of 0.05 ppm.
采用流动电势法和负性聚苯乙烯胶乳颗粒沉积法对分子量为70,000的阳离子聚电解质聚烯丙胺盐酸盐(PAH)在云母上的吸附进行了表征。通过测定表面zeta电位的表观zeta电位随本体PAH浓度的变化来跟踪PAH层的形成。zeta电位是根据在由两层预先覆盖有聚电解质的云母板形成的平行板通道中测量的流动电势计算得出的。实验数据表示为还原zeta电位zeta/zeta0对PAH覆盖率Theta(PAH)的依赖性,该覆盖率是使用对流扩散理论计算得出的。结果发现,对于10^(-2) M的离子强度,zeta/zeta0对Theta(PAH)的依赖性可以由先前为被胶体颗粒覆盖的表面建立的理论模型来反映。电动测量通过在PAH覆盖的云母表面上进行的颗粒沉积实验得到补充。发现聚合物覆盖率与颗粒的初始沉积速率以及堵塞覆盖率之间存在直接相关性。当ThetaPAH > 0.3时,初始沉积速率达到了对流扩散理论预测的均匀表面的值。将PAH改性表面的初始沉积速率与先前通过胶体颗粒预吸附形成的异质表面获得的实验和理论结果进行了比较。结果表明,负性胶乳沉积发生在表现出负表观zeta电位的表面上,这解释了先前工作中观察到的颗粒异常沉积现象。有人提出,结合电动和颗粒沉积方法可用于检测表面吸附的聚电解质,其覆盖率范围可达百分之几。这使得能够测量0.05 ppm水平的本体聚电解质浓度。