Interaction forces between colloidal particles in a solution of like-charged, adsorbing nanoparticles

被引:42
|
作者
Mckee, Clayton T. [1 ]
Walz, John Y. [1 ]
机构
[1] Virginia Tech, Dept Chem Engn, Blacksburg, VA 24061 USA
基金
美国国家科学基金会;
关键词
Depletion forces; Colloidal probe atomic force microscopy; Binary colloidal systems; Interparticle forces; Colloidal forces; STABILIZED LATEX DISPERSIONS; DEPLETION INTERACTION; FREE POLYMER; AQUEOUS SYSTEMS; SURFACES; FLOCCULATION; MICROSCOPE; POLYDISPERSITY; ELECTROLYTE; SPHEROIDS;
D O I
10.1016/j.jcis.2011.09.015
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
We have measured the force between a weakly charged micron-sized colloidal particle and flat substrate in the presence of highly charged nanoparticles of the same sign under solution conditions such that the nanoparticles physically adsorb to the colloidal particle and substrate. The objective was to investigate the net effect on the force profile between the microparticle and flat substrate arising from both nanoparticle adsorption and nanoparticles in solution. The experiments used colloidal probe atomic force microscopy (CP-AFM) to measure the force profile between a relatively large (5 mu m) colloidal probe glass particle and a planar glass substrate in aqueous solutions at varying concentrations of spherical nanoparticles. At very low nanoparticle concentrations, the primary effect was an increase in the electrostatic repulsion between the surfaces due to adsorption of the more highly charged nanoparticles. As the nanoparticle concentration is increased, a depletion attraction formed, followed by longer-range structural forces at the highest nanoparticle concentrations studied. These results suggest that, depending on their concentration, such nanoparticles can either stabilize a dispersion of weakly-charged colloidal particles or induce flocculation. This behavior is qualitatively different from that in nonadsorbing systems, where the initial effect is the development of an attractive depletion force. (C) 2011 Published by Elsevier Inc.
引用
收藏
页码:72 / 80
页数:9
相关论文
共 50 条
  • [31] INTERACTION BETWEEN CHARGED RODLIKE COLLOIDAL PARTICLES
    LOWEN, H
    PHYSICAL REVIEW LETTERS, 1994, 72 (03) : 424 - 427
  • [32] Effect of confinement on the interaction between two like-charged rods
    Odriozola, G.
    Jimenez-Angeles, F.
    Lozada-Cassou, M.
    PHYSICAL REVIEW LETTERS, 2006, 97 (01)
  • [33] Adsorption of surfactant molecules onto the surface of colloidal particles: Case of like-charged species
    Correia, Elton L.
    Thakur, Siddharth
    Ervin, Aanahita
    Shields, Emma
    Razavi, Sepideh
    COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2023, 676
  • [34] Multivalent Ion-Mediated Attraction between Like-Charged Colloidal Particles: Nonmonotonic Dependence on the Particle Charge
    Lin, Cheng
    Qiang, Xiaowei
    Dong, Hai-Long
    Huo, Jie
    Tan, Zhi-Jie
    ACS OMEGA, 2021, 6 (14): : 9876 - 9886
  • [35] The apparent attraction between like-charged particles next to an oppositely charged planar surface
    Trokhymchuk, A
    Henderson, D
    Sovyak, E
    Wasan, DT
    JOURNAL OF MOLECULAR LIQUIDS, 2004, 109 (02) : 109 - 113
  • [36] Like-charged particles at liquid interfaces - Reply
    Nikolaides, MG
    Bausch, AR
    Hsu, MF
    Dinsmore, AD
    Brenner, MP
    Gay, C
    Weitz, DA
    NATURE, 2003, 424 (6952) : 1014 - 1014
  • [37] Brownian coagulation of like-charged aerosol particles
    Patra, Pijush
    Roy, Anubhab
    PHYSICAL REVIEW FLUIDS, 2022, 7 (06)
  • [38] Interaction between like-charged particles at a liquid interface: Electrostatic repulsion vs. electrocapillary attraction
    Danov, Krassimir D.
    Kralchevsky, Peter A.
    JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2010, 345 (02) : 505 - 514
  • [39] Forces between like-charged walls in an electrolyte solution: A comparison of McMillan-Mayer results for several models
    Otto, F
    Patey, GN
    JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (07): : 2851 - 2855
  • [40] Forces between like-charged walls in electrolyte solution: Molecular solvent effects at the McMillan-Mayer level
    Otto, F
    Patey, GN
    JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (20): : 8939 - 8949