Aggregation and disaggregation of ZnO nanoparticles: Influence of pH and adsorption of Suwannee River humic acid

被引:250
作者
Omar, Fatehah Mohd [1 ]
Aziz, Hamidi Abdul [2 ]
Stoll, Serge [1 ]
机构
[1] Univ Geneva, FA Forel Inst, CH-1209 Versoix, Switzerland
[2] Univ Sains Malaysia, Sch Civil Engn, Nibong Tebal 14300, Penang, Malaysia
基金
瑞士国家科学基金会;
关键词
ZnO nanoparticles; Suwannee River humic acid; Zeta potential; Aggregation; Disaggregation; METAL-OXIDE NANOPARTICLES; ZINC-OXIDE; SURFACE; DISSOLUTION; STABILITY; CHEMISTRY; KINETICS; WATER; SIZE;
D O I
10.1016/j.scitotenv.2013.08.044
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The surface charge and average size of manufactured ZnO nanoparticles (NPs) were studied as a function of pH to understand the aggregation behavior and importance of the electrostatic interactions in solution. The interactions between ZnO and Suwannee River humic acid (SRHA) were then investigated under a range of environmentally relevant conditions with the ZnO nanoparticles pH(pzc) as the point of reference. The anionic charges carried by aquatic humic substances were found to play a major role in the aggregation and disaggregation of ZnO nanoparticles. At low concentrations of SRI-IA (<0.05 mg/L) and below the pH(pzc), anionic SRHA was rapidly adsorbed onto the positively charged ZnO NPs hence promoting aggregation. With similar SHRA concentrations, at pH(pzc), SRHA was able to control the suspension behavior of the ZnO and promote partial disaggregation in small volumes. This was more distinguishable when the pH was greater than pH(pzc) as SRHA formed a surface coating on the ZnO nanoparticles and enhanced stability via electrostatic and steric interactions. In most cases, the NP coating by SRHA induced disaggregation behavior in the ZnO nanoparticles and decreased the aggregate size in parallel to increasing SRHA concentrations. Results also suggest that environmental aquatic concentration ranges of humic acids largely modify the stability of aggregated or dispersed ZnO nanoparticles. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 201
页数:7
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