Experimental study of electrostatically stabilized colloidal particles: Colloidal stability and charge reversal

被引:111
作者
Schneider, Christian [1 ,2 ]
Hanisch, Mathias [3 ]
Wedel, Bastian [3 ]
Jusufi, Arben [4 ]
Ballauff, Matthias [1 ,2 ]
机构
[1] Humboldt Univ, Dept Phys, D-12489 Berlin, Germany
[2] Helmholtz Zentrum Berlin, D-14109 Berlin, Germany
[3] Univ Bayreuth, D-95440 Bayreuth, Germany
[4] Temple Univ, Inst Computat Mol Sci, Philadelphia, PA 19122 USA
关键词
DLVO theory; Zeta potential; Diffuse potential; Colloidal stability; Charge reversal; Charge inversion; Multivalent counterions; Microsurface potential measurements; Counterion adsorption; Counterion correlations; Poisson-Boltzmann; Simultaneous static and dynamic light scattering; Electrostatic stabilization; ION-ION CORRELATION; COAGULATION RATE; MULTIVALENT COUNTERIONS; LIGHT-SCATTERING; MODEL COLLOIDS; SURFACE-CHARGE; REAL COLLOIDS; DLVO THEORY; AGGREGATION; INVERSION;
D O I
10.1016/j.jcis.2011.02.039
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 consider the interaction of colloidal spheres in the presence of mono-, di-, and trivalent ions. The colloids are stabilized by electrostatic repulsion due to surface charges. The repulsive part of the interaction potential Psi(d) is deduced from precise measurements of the rate of slow coagulation. These "microsurface potential measurements" allow us to determine a weak repulsion in which Psi(d) is of the order of a few k(B)T. These data are compared to zeta potential measured under similar conditions. At higher concentrations both di- and trivalent counterions accumulate at the very proximity of the particle surface leading to charge reversal. The salt concentration c(cr) at which charge reversal occurs is found to be always above the critical coagulation concentration c(ccc). The analysis of Psi(d) and of the zeta potential demonstrates, however, that adsorption of multivalent counterions starts far below c(cr). Hence, colloid stability in the presence of di- and trivalent ions cannot be described in terms of a DLVO ansatz assuming a surface charge that is constant with regard to the ionic strength. (c) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:62 / 67
页数:6
相关论文
共 43 条
[1]  
[Anonymous], 1948, Theory of the Stability of Lyophobic Colloids
[2]   Charging and aggregation properties of carboxyl latex particles: Experiments versus DLVO theory [J].
Behrens, SH ;
Christl, DI ;
Emmerzael, R ;
Schurtenberger, P ;
Borkovec, M .
LANGMUIR, 2000, 16 (06) :2566-2575
[3]   Aggregation in charge-stabilized colloidal suspensions revisited [J].
Behrens, SH ;
Borkovec, M ;
Schurtenberger, P .
LANGMUIR, 1998, 14 (08) :1951-1954
[4]   Influence of the secondary interaction energy minimum on the early stages of colloidal aggregation [J].
Behrens, SH ;
Borkovec, M .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2000, 225 (02) :460-465
[5]   Charge inversion by multivalent ions: Dependence on dielectric constant and surface-charge density [J].
Besteman, K ;
Zevenbergen, MAG ;
Lemay, SG .
PHYSICAL REVIEW E, 2005, 72 (06)
[6]   Direct observation of charge inversion by multivalent ions as a universal electrostatic phenomenon [J].
Besteman, K ;
Zevenbergen, MAG ;
Heering, HA ;
Lemay, SG .
PHYSICAL REVIEW LETTERS, 2004, 93 (17) :170802-1
[7]   Simplifications of the Poisson-Boltzmann equation for the electrostatic interaction of close hydrophilic surfaces in water [J].
Biesheuvel, PM .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2001, 238 (02) :362-370
[8]   Measurement and interpretation of electrokinetic phenomena [J].
Delgado, A. V. ;
Gonzalez-Caballero, F. ;
Hunter, R. J. ;
Koopal, L. K. ;
Lyklema, J. .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2007, 309 (02) :194-224
[9]   FORCES BETWEEN ALUMINA SURFACES IN SALT-SOLUTIONS - NON-DLVO FORCES AND THE IMPLICATIONS FOR COLLOIDAL PROCESSING [J].
DUCKER, WA ;
XU, Z ;
CLARKE, DR ;
ISRAELACHVILI, JN .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1994, 77 (02) :437-443
[10]  
Evans DF., 1999, COLLOIDAL DOMAIN