Adsorption of ionic surfactants in particulate systems: flotation, stability, and interaction forces

被引:58
作者
Bremmell, KE [1 ]
Jameson, GJ
Biggs, S
机构
[1] Univ Newcastle, Dept Chem, Ctr Multiphase Proc, Callaghan, NSW 2308, Australia
[2] Univ Newcastle, Dept Chem Engn, Callaghan, NSW 2308, Australia
关键词
ionic surfactants; adsorption; direct interaction forces; electrophoretic mobility; stability; flotation;
D O I
10.1016/S0927-7757(98)00802-4
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
The flotation efficiency of silica particles using the ionic surfactants, sodium dodecylbenzenesulfonate (SDbS) and cetyltrimethylammonium bromide (CPB), have been investigated. Results from adsorption, electrophoretic mobility, dispersion stability and direct interaction force measurements are used to develop an understanding of the role of ionic surfactants in particulate flotation. Adsorption and mobility data indicate that SDbS adsorbs at the silica/solution interface, though without improving the flotation efficiency. CPB was found to adsorb on the silica particles as a result of electrostatic interaction; initially to neutralize the surface charge and destabilize the suspension, and at higher surfactant concentrations, to reverse the particle charge and re-stabilize the suspension. Direct force measurements in the presence of CPB confirm that the electrostatic interactions between approaching surfaces are neutralized at low CPB concentrations. Additionally, evidence for a strong adhesive interaction after contact is seen. At higher concentrations, the surfaces begin to recharge, and the adhesive interaction decreases in magnitude. The flotation efficiency was found to correlate well with the measured particle interactions, and to be a function of the particulate electrophoretic mobility. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:75 / 87
页数:13
相关论文
共 35 条
[1]   LONG-RANGE ATTRACTION BETWEEN HYDROPHOBIC SURFACES [J].
ATTARD, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (17) :6441-6444
[2]   MEASUREMENT OF THE FORCES BETWEEN GOLD SURFACES IN WATER BY ATOMIC-FORCE MICROSCOPY [J].
BIGGS, S ;
MULVANEY, P .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (11) :8501-8505
[3]   EFFECTS OF COUNTERIONS ON SURFACTANT SURFACE AGGREGATES AT THE ALUMINA AQUEOUS-SOLUTION INTERFACE [J].
BITTING, D ;
HARWELL, JH .
LANGMUIR, 1987, 3 (04) :500-511
[4]   EXAMINATION OF THE GEOMETRY OF LONG-RANGE TIP SAMPLE INTERACTION IN ATOMIC-FORCE MICROSCOPY [J].
DRUMMOND, CJ ;
SENDEN, TJ .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1994, 87 (03) :217-234
[5]   Surface-aggregate shape transformation [J].
Ducker, WA ;
Wanless, EJ .
LANGMUIR, 1996, 12 (24) :5915-5920
[6]   MEASUREMENT OF FORCES IN LIQUIDS USING A FORCE MICROSCOPE [J].
DUCKER, WA ;
SENDEN, TJ ;
PASHLEY, RM .
LANGMUIR, 1992, 8 (07) :1831-1836
[7]   A PHENOMENOLOGICAL THEORY OF LONG-RANGE HYDROPHOBIC ATTRACTION FORCES BASED ON A SQUARE-GRADIENT VARIATIONAL APPROACH [J].
ERIKSSON, JC ;
LJUNGGREN, S ;
CLAESSON, PM .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1989, 85 :163-176
[8]   Characterization of adsorption of quaternary ammonium cationic surfactants and their adsolubilization behaviors on silica [J].
Esumi, K ;
Matoba, M ;
Yamanaka, Y .
LANGMUIR, 1996, 12 (09) :2130-2135
[9]  
FUERSTENAU DW, 1964, T SOC MIN ENG, V229, P321
[10]  
GAUDIN AM, 1955, T AM I MIN MET ENG, V202, P958