Sander Sylvia, Mosley Luke M, Hunter Keith A
Department of Chemistry, University of Otago, P.O. Box 56, Dunedin, New Zealand.
Environ Sci Technol. 2004 Sep 15;38(18):4791-6. doi: 10.1021/es049602z.
The nature of interparticle forces acting on colloid particle surfaces with adsorbed surface films of the internationally used humic acid standard material, Suwannee River Humic Acid (SHA), has been investigated using an atomic force microscope (AFM). Two particle surfaces were used, alumina and a hydrous iron oxide film coated onto silica particles. Adsorbed SHA dominated the interactive forces for both surface types when present. At low ionic strength and pH > 4, the force curves were dominated by electrostatic repulsion of the electrical double layers, with the extent of repulsion decreasing as electrolyte (NaCl) concentration increased, scaling with the Debye length (kappa(-1)) of the electrolyte according to classical theory. At pH approximately 4, electrostatic forces were largely absent, indicating almost complete protonation of carboxylic acid (-COOH) functional groups on the adsorbed SHA. Under these conditions and also at high electrolyte concentration ([NaCl] > 0.1 M), the absence of electrostatic forces allowed observation of repulsion forces arising from steric interaction of adsorbed SHA as the oxide surfaces approached closely to each other (separation < 10 nm). This steric barrier shrank as electrolyte concentration increased, implying tighter coiling of the adsorbed SHA molecules. In addition, adhesive bridging between surfaces was observed only in the presence of SHA films, implying a strong energy barrier to spontaneous detachment of the surfaces from each other once joined. This adhesion was especially strong in the presence of Ca2+ which appears to bridge SHA layers on each surface. Overall, our results show that SHA is a good model for the NOM adsorbed on colloids.
利用原子力显微镜(AFM)研究了国际上通用的腐殖酸标准物质——苏万尼河腐殖酸(SHA)吸附在胶体颗粒表面时,颗粒间作用力的性质。使用了两种颗粒表面,即氧化铝以及涂覆在二氧化硅颗粒上的水合氧化铁膜。当存在吸附的SHA时,它主导了两种表面类型的相互作用力。在低离子强度和pH > 4时,力曲线主要由双电层的静电排斥作用主导,随着电解质(NaCl)浓度的增加,排斥程度降低,根据经典理论,其与电解质的德拜长度(κ⁻¹)成比例。在pH约为4时,静电作用力基本不存在,这表明吸附的SHA上的羧酸(-COOH)官能团几乎完全质子化。在这些条件下以及在高电解质浓度([NaCl] > 0.1 M)时,由于静电作用力不存在,当氧化物表面彼此靠近(间距 < 10 nm)时,可以观察到由吸附的SHA的空间相互作用产生的排斥力。随着电解质浓度的增加,这种空间位垒缩小,这意味着吸附的SHA分子的卷曲更紧密。此外,仅在存在SHA膜的情况下观察到表面之间的粘附桥连,这意味着一旦结合,表面彼此自发分离存在很强的能垒。在Ca²⁺存在的情况下,这种粘附力特别强,Ca²⁺似乎在每个表面上桥连SHA层。总体而言,我们的结果表明,SHA是吸附在胶体上的天然有机物的良好模型。