Dielectric spectroscopy and electrophoretic mobility measurements interpreted with the standard electrokinetic model

被引:38
作者
Hollingsworth, AD [1 ]
Saville, DA [1 ]
机构
[1] Princeton Univ, Dept Chem Engn, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
dielectric response of colloidal suspension; impedance analyzer; variable spacing dielectric cells; electrophoresis; standard electrokinetic model; electrokinetics;
D O I
10.1016/j.jcis.2003.08.032
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 report results from complementary electrokinetic measurements-dielectric relaxation and electrophoretic mobility-undertaken to test the applicability of the standard electrokinetic theory with a model system. Dielectric spectra were obtained at frequencies between 1 kHz and 40 MHz with a new, two-electrode cell design [Hollingsworth and Saville, J. Colloid Interface Sci. 257 (2003) 65-76]; mobility data were acquired with an electrophoretic light scattering instrument. Data from the two-electrode cell were collected at different electrode separations and interpreted with newly developed procedures to remove the influence of electrode polarization. Methodology A employs extrapolation to infinite electrode separation to compute the dielectric constant and conductivity as functions of frequency. The contributions from suspended particles are reported in terms of dielectric constant and conductivity increments. Methodology B uses a theoretical model of electrode polarization and the standard electrokinetic model in a nonlinear regression scheme. Results are presented in several forms: frequency-dependent dielectric constant and conductivity increments, frequency-dependent dielectric constants and conductivities, and the complex dipole coefficient. It is shown that the standard model provides a consistent methodology for interpreting particle behavior; zeta-potentials inferred from mobility and dielectric relaxation agree to within experimental error. Moreover, the cell design and interpretation are straightforward and provide relatively simple ways to obtain complementary measurements over a wide frequency range. The results unambiguously show that electrokinetic character of this dispersion follows the standard model. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:235 / 245
页数:11
相关论文
共 28 条
[1]   Micro total analysis systems. 2. Analytical standard operations and applications [J].
Auroux, PA ;
Iossifidis, D ;
Reyes, DR ;
Manz, A .
ANALYTICAL CHEMISTRY, 2002, 74 (12) :2637-2652
[2]   DIELECTRIC-RELAXATION OF COLLOIDAL PARTICLE SUSPENSIONS AT RADIO FREQUENCIES CAUSED BY SURFACE CONDUCTANCE [J].
BLUM, G ;
MAIER, H ;
SAUER, F ;
SCHWAN, HP .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (02) :780-789
[3]   Observation of the mobility maximum predicted by the standard electrokinetic model for highly charged amidine latex particles [J].
Borkovec, M ;
Behrens, SH ;
Semmler, M .
LANGMUIR, 2000, 16 (11) :5209-5212
[4]   DIELECTRIC RESPONSE AND CONDUCTIVITY OF DILUTE SUSPENSIONS OF COLLOIDAL PARTICLES [J].
DELACEY, EHB ;
WHITE, LR .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1981, 77 :2007-2039
[5]   ELECTROPHORETIC MOBILITY AND DIELECTRIC RESPONSE MEASUREMENTS ON ELECTROKINETICALLY IDEAL POLYSTYRENE LATEX-PARTICLES [J].
GITTINGS, MR ;
SAVILLE, DA .
LANGMUIR, 1995, 11 (03) :798-800
[6]   Polarizaability and complex conductivity of dilute suspensions of spherical colloidal particles with charged (polyelectrolyte) coatings [J].
Hill, RJ ;
Saville, DA ;
Russel, WB .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 263 (02) :478-497
[7]   A broad frequency range dielectric spectrometer for colloidal suspensions: cell design, calibration, and validation [J].
Hollingsworth, AD ;
Saville, DA .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 257 (01) :65-76
[8]   LOW-FREQUENCY DIELECTRIC-RELAXATION OF HEMATITE AND SILICA SOLS [J].
KIJLSTRA, J ;
VANLEEUWEN, HP ;
LYKLEMA, J .
LANGMUIR, 1993, 9 (07) :1625-1633
[9]   EFFECTS OF SURFACE CONDUCTION ON THE ELECTROKINETIC PROPERTIES OF COLLOIDS [J].
KIJLSTRA, J ;
VANLEEUWEN, HP ;
LYKLEMA, J .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1992, 88 (23) :3441-3449
[10]  
Lyklema J., 1995, Fundamentals of Interface and Colloid Science, V1-2