Relation between the Surface Tension and Roughness of the Intrinsic Liquid Surface

被引:8
作者
Jedlovszky, Pal [1 ,2 ,3 ]
Darvas, Maria [4 ]
Horvai, George [2 ,5 ]
机构
[1] Eotvos Lorand Univ, Inst Chem, Lab Interfaces & Nanosize Syst, H-1117 Budapest, Hungary
[2] MTA BME Res Grp Tech Analyt Chem, H-1111 Budapest, Hungary
[3] EKF Dept Chem, H-3300 Eger, Hungary
[4] SISSA, Dept Biol & Stat Phys, I-34014 Trieste, Italy
[5] Budapest Univ Technol & Econ, Dept Inorgan & Analyt Chem, H-1111 Budapest, Hungary
来源
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION A-A JOURNAL OF PHYSICAL SCIENCES | 2013年 / 68卷 / 1-2期
关键词
Liquid-Vapour Interface; Surface Tension; Surface Roughness; Computer Simulation; MOLECULAR-DYNAMICS SIMULATIONS; VAPOR INTERFACE; COMPUTER-SIMULATION; WATER; EQUILIBRIUM; ETHANOL; TEMPERATURE; ADSORPTION; DEPENDENCE; SOLVATION;
D O I
10.5560/ZNA.2012-0096
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
Previously published computer simulation data concerning the surface tension and surface roughness of various different liquid systems (i. e., binary water-methanol and water-dimethyl sulphoxide (DMSO) mixtures, water-poly-(ethylene-oxide) systems containing adsorbed sodium dodecyl sulphate, and room temperature ionic liquids) are re-analysed in order to find a relation between these quantities. It is found that the amplitude of the molecularly wavy liquid surface is inversely proportional to the logarithm of the surface tension while no clear correlation between the periodicity of the wavy surface and the surface tension is observed. It is also seen that the determination of the roughness parameters in a way analogous with the Langmuir formalism results in considerably more robust values than when an extra parameter is introduced in the procedure using a formula in analogy with the Langmuir-Freundlich isotherm.
引用
收藏
页码:123 / 129
页数:7
相关论文
共 42 条
[1]   Structure, thermodynamics, and dynamics of the liquid/vapor interface of water/dimethylsulfoxide mixtures [J].
Benjamin, I .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (16) :8070-8079
[2]   VIBRATIONAL-SPECTRUM OF WATER AT THE LIQUID/VAPOR INTERFACE [J].
BENJAMIN, I .
PHYSICAL REVIEW LETTERS, 1994, 73 (15) :2083-2086
[3]   Intrinsic profiles beyond the capillary wave theory:: A Monte Carlo study -: art. no. 166103 [J].
Chacón, E ;
Tarazona, P .
PHYSICAL REVIEW LETTERS, 2003, 91 (16)
[4]   The intrinsic structure of the water surface [J].
Chacon, Enrique ;
Tarazona, Pedro ;
Alejandre, Jose .
JOURNAL OF CHEMICAL PHYSICS, 2006, 125 (01)
[5]   MOLECULAR-DYNAMICS SIMULATIONS OF LIQUID, INTERFACE, AND IONIC SOLVATION OF POLARIZABLE CARBON-TETRACHLORIDE [J].
CHANG, TM ;
PETERSON, KA ;
DANG, LX .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (17) :7502-7513
[6]   Computer simulation of chloroform with a polarizable potential model [J].
Chang, TM ;
Dang, LX ;
Peterson, KA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (17) :3413-3419
[7]   Water-hydrocarbon interfaces: Effect of hydrocarbon branching on interfacial structure [J].
Chowdhary, Janamejaya ;
Ladanyi, Branka M. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (31) :15442-15453
[8]  
Daillant J., 1999, XRAY NEUTRON REFLECT
[9]   Many-body interactions in liquid methanol and its liquid/vapor interface: A molecular dynamics study [J].
Dang, LX ;
Chang, TM .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (18) :9851-9857
[10]   Competitive Adsorption of Surfactants and Polymers at the Free Water Surface. A Computer Simulation Study of the Sodium Dodecyl Sulfate- Poly(ethylene oxide) System [J].
Darvas, Maria ;
Tibor Gilanyi ;
Pal Jedlovszky .
JOURNAL OF PHYSICAL CHEMISTRY B, 2011, 115 (05) :933-944