Monte Carlo simulations of the electrical double layer forces in the presence of divalent electrolyte solutions: effect of the ion size

被引:19
作者
Martin-Molina, Alberto [2 ]
Guadalupe Ibarra-Armenta, Jose [1 ]
Gonzalez-Tovar, Enrique [2 ,3 ]
Hidalgo-Alvarez, Roque [2 ]
Quesada-Perez, Manuel [1 ]
机构
[1] Univ Jaen, Dept Fis, Escuela Politecn Super Linares, Jaen 23700, Spain
[2] Univ Granada, Fac Ciencias, Grp Fis Fluidos & Biocoloides, Dept Fis Aplicada, E-18071 Granada, Spain
[3] Univ Autonoma San Luis Potosi, Inst Fis, San Luis Potosi 78000, Mexico
关键词
MEAN FORCE; AQUEOUS-ELECTROLYTE; CHARGED INTERFACES; MICA SURFACES; ATTRACTION; COLLOIDS; BEHAVIOR; MODEL; STABILITY; MACROIONS;
D O I
10.1039/c0sm00609b
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
In this paper, the effect of ion size on the mean forces between two charged plates in the presence of divalent counterions is analyzed with the help of Monte Carlo simulations in the framework of the primitive model. Inspired by a preliminary work in which a particular and isolated case was presented, we propose a more systematic survey considering both like and oppositely charged plates, different surface charge densities (with magnitudes ranging from 0.01 to 0.2 Cm-2) and two very different ionic strengths (0.5 and 500 mM). The effect of ion size is probed comparing systematically results for the most commonly used ionic diameter (0.425 nm) and greater values reported in the scientific literature for hydrated ions. These greater values were previously and successfully employed in other areas (e.g., electrokinetic behaviour in the presence of divalent and trivalent ions). Our simulations show that force-distance profiles strongly depend on the ion size. Consequently, some of the 'classical' findings obtained from simulations must be carefully reconsidered. In particular, the widely known and reported attraction between like-charged plates (or macroions) becomes repulsion with increasing ion size.
引用
收藏
页码:1441 / 1449
页数:9
相关论文
共 56 条
[31]   The individual and mean activity coefficients of an electrolyte from the inverse GCMC simulation [J].
Lamperski, S. .
MOLECULAR SIMULATION, 2007, 33 (15) :1193-1198
[32]   Electrostatic correlations: from plasma to biology [J].
Levin, Y .
REPORTS ON PROGRESS IN PHYSICS, 2002, 65 (11) :1577-1632
[33]   Electrostatic attraction and phase separation in solutions of like-charged colloidal particles [J].
Linse, P ;
Lobaskin, V .
PHYSICAL REVIEW LETTERS, 1999, 83 (20) :4208-4211
[34]   Simulating prescribed particle densities in the grand canonical ensemble using iterative algorithms [J].
Malasics, Attila ;
Gillespie, Dirk ;
Boda, Dezso .
JOURNAL OF CHEMICAL PHYSICS, 2008, 128 (12)
[35]   An efficient iterative grand canonical Monte Carlo algorithm to determine individual ionic chemical potentials in electrolytes [J].
Malasics, Attila ;
Boda, Dezso .
JOURNAL OF CHEMICAL PHYSICS, 2010, 132 (24)
[36]   Charge reversal in real colloids:: Experiments, theory and simulations [J].
Martin-Molina, Alberto ;
Alberto Maroto-Centeno, Jose ;
Hidalgo-Alvarez, Roque ;
Quesada-Perez, Manuel .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 319 (1-3) :103-108
[37]   Effect of Ion Dispersion Forces on the Electric Double Layer of Colloids: A Monte Carlo Simulation Study [J].
Martin-Molina, Alberto ;
Ibarra-Armenta, Jose G. ;
Quesada-Perez, Manuel .
JOURNAL OF PHYSICAL CHEMISTRY B, 2009, 113 (08) :2414-2421
[38]   (N,V,T) Monte Carlo study of the electrostatic forces between charged lamellae: Influence of surface charge localization [J].
Meyer, S ;
Delville, A .
LANGMUIR, 2001, 17 (23) :7433-7438
[40]   Ion-ion correlation attraction in a molecular solvent [J].
Pegado, Luis ;
Jonsson, Bo ;
Wennerstrom, Hakan .
JOURNAL OF CHEMICAL PHYSICS, 2008, 129 (18)