Evaluation of particle deposition in aqueous solutions by the quartz crystal microbalance method

被引:11
作者
Gotoh, K [1 ]
Nakata, Y
Tagawa, M
机构
[1] Kyoto Univ, Fushimi Ku, Kyoto 6128522, Japan
[2] Kobe Univ Fash & Design, Akashi, Hyogo 6730001, Japan
[3] Kanazawa Inst Technol, Nonoichi, Ishikawa 9218501, Japan
关键词
particle deposition; quartz crystal microbalance; surface free energy; extended DLVO theory; acid-base interaction;
D O I
10.1016/j.colsurfa.2005.07.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Concerning the redeposition of particulate soils in aqueous solutions was in the detergent process, particle deposition onto substrates investigated by the application of the quartz crystal microbalance (QCM) technique, and the effects of the kinds of the particle and substrate and the addition of ethanol were discussed by the extended DLVO theory. The film of polyethylene, Nylon 6 or cellulose acetate as a substrate was prepared on the gold electrode of the QCM by a spin-coating method. The electrode with or without the polymer film was perpendicularly immersed in the aqueous dispersion of spherical polyethylene or nylon particles. The total mass of particles deposited onto the electrode was determined, in situ, from frequency change of the QCM. The deposited mass was also determined from the difference in frequency measured in air before and after the immersion in the dispersion. In both cases, the particle deposition increased with immersion time and attained apparent equilibrium after 30-60 min. Apparent equilibrium deposition was large for the polyethylene particle compared with the Nylon 12 particle. For either particle, a considerable difference in the deposited amount was observed among the substrates. In all systems, the particle deposition drastically decreased by addition of ethanol to the aqueous dispersion. The results were discussed in terms of the electrical double layer, the Lifshitz-van der Waals and acid-base interactions between the particle and the substrate, which were calculated using the experimentally determined surface free energy components and electrokinetic potentials. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 123
页数:7
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