Dipolar anions are not preferentially attracted to the oil/water interface

被引:27
作者
Beattie, JK [1 ]
Djerdjev, AM
Franks, GV
Warr, GG
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Univ Newcastle, Dept Chem Engn, Newcastle, NSW 2308, Australia
关键词
D O I
10.1021/jp052894l
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
Homogenization of hexadecane in water at pH 9 gives the same surface charge density in the presence of 0.2 mM thiocyanate or acetate anions as in the presence of chloride, indicating that these dipolar anions are not preferentially adsorbed at the oil/water interface. The decrease in the zeta potential of the emulsion droplets as the sodium salts of iodate, thiocyanate, or acetate are added from 0.1 to 10 mM is the same as that when sodium chloride is added, leading to the same conclusion. Increasing the sodium hydroxide concentration from pH 9 to 11.5 has a different effect on the zeta potential, consistent with the specific adsorption of hydroxide ion at the oil/water interface.
引用
收藏
页码:15675 / 15676
页数:2
相关论文
共 22 条
[1]   The pristine oil/water interface: Surfactant-free hydroxide-charged emulsions [J].
Beattie, JK ;
Djerdjev, AM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (27) :3568-3571
[2]   The electrophoresis of certain hydrocarbons and their simple derivatives as a function of (pH). [J].
Carruthers, JC .
TRANSACTIONS OF THE FARADAY SOCIETY, 1938, 34 (01) :0300-0307
[3]   Solvation structure and mobility mechanism of OH-:: A Car-Parrinello molecular dynamics investigation of alkaline solutions [J].
Chen, B ;
Ivanov, I ;
Park, JM ;
Parrinello, M ;
Klein, ML .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (46) :12006-12016
[4]   New insight into the orientational order of water molecules at the water/1,2-dichloroethane interface: A Monte Carlo simulation study [J].
Jedlovszky, P ;
Vincze, A ;
Horvai, G .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (05) :2271-2280
[5]   The hydrophobic effect: Molecular dynamics simulations of water confined between extended hydrophobic and hydrophilic surfaces [J].
Jensen, MO ;
Mouritsen, OG ;
Peters, GH .
JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (20) :9729-9744
[6]   An ab initio molecular dynamics study of the aqueous liquid-vapor interface [J].
Kuo, IFW ;
Mundy, CJ .
SCIENCE, 2004, 303 (5658) :658-660
[7]   SYSTEMATIC STUDY OF MOLECULAR ANIONS WITHIN THE SELF-CONSISTENT-FIELD APPROXIMATION - OH-, CN-, C2H-, NH2-, AND CH3- [J].
LEE, TJ ;
SCHAEFER, HF .
JOURNAL OF CHEMICAL PHYSICS, 1985, 83 (04) :1784-1794
[8]   Water at hydrophobic substrates: Curvature, pressure, and temperature effects [J].
Mamatkulov, SI ;
Khabibullaev, PK ;
Netz, RR .
LANGMUIR, 2004, 20 (11) :4756-4763
[9]   SOLUTE ORIENTATIONAL DYNAMICS AND SURFACE-ROUGHNESS OF WATER HYDROCARBON INTERFACES [J].
MICHAEL, D ;
BENJAMIN, I .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (05) :1530-1536
[10]   Structural characterization of the H2O/CCl4 liquid interface using molecular dynamics simulations [J].
Moreira, NH ;
Skaf, MS .
SURFACE AND COLLOID SCIENCE, 2004, 128 :81-85