Effects of Temperature and Pore Size on Water Diffusion Inside Carbon Nanotubes

Author(s):  
Kuiwen Zhao ◽  
Zhenyu Liu ◽  
Huiying Wu

Nanotube membranes show exceptional transport properties for water and other substances, which can be utilized in many attractive applications, such as molecular sieving, drug delivery, and water purification. To design effective nanotube membranes for these applications, it is necessary to understand the transport properties of water confined in nanotubes. The diffusion of water inside nanotubes plays an important role in this process. By performing extensive molecular dynamics simulations, we investigate the effects of temperature and pore size on water diffusion inside carbon nanotubes. The results demonstrate that the temperature dependence of self-diffusion coefficient of water inside carbon nanotubes is obviously different for various pore sizes. It can be found that for nanotube with diameter of 0.681 nm and 0.820–0.905 nm, the self-diffusion coefficient decreases remarkably with the decreasing temperature due to the change of water structure, which is not obvious for water in nanotubes with other pore sizes. This fundamental study attempts to provide deep insights in understanding the transport process across nanotube membranes.

2019 ◽  
Vol 65 (2) ◽  
pp. 190
Author(s):  
F. De J. Guevara Rodríguez

In this work, the effect of pore structure of a sandstone on the molecular displacement of confined methane gas is analyzed. It was found that the self-diffusion coefficient of a methane molecule depends on the pore size distribution an their connectivity. In particular, the time dependent self-diffusion coefficient exhibits a maximum which is correlated with the effect of the molecular confinement. It was found that a sandstone with small pores and/or pores bad connected traps the gas more efficiently than other pores structures. This fact enable to understand the scattered values which the residual trapped gas saturation measures exhibit with different sandstones.


Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 4030
Author(s):  
Gengbiao Chen ◽  
Zhiwen Liu

The diffusion behavior of fluid water in nanochannels with hydroxylation of silica gel and silanization of different modified chain lengths was simulated by the equilibrium molecular dynamics method. The diffusion coefficient of fluid water was calculated by the Einstein method and the Green–Kubo method, so as to analyze the change rule between the modification degree of nanochannels and the diffusion coefficient of fluid water. The results showed that the diffusion coefficient of fluid water increased with the length of the modified chain. The average diffusion coefficient of fluid water in the hydroxylated nanochannels was 8.01% of the bulk water diffusion coefficient, and the diffusion coefficients of fluid water in the –(CH2)3CH3, –(CH2)7CH3, and –(CH2)11CH3 nanochannels were 44.10%, 49.72%, and 53.80% of the diffusion coefficients of bulk water, respectively. In the above four wall characteristic models, the diffusion coefficients in the z direction were smaller than those in the other directions. However, with an increase in the silylation degree, the increased self-diffusion coefficient due to the surface effect could basically offset the decreased self-diffusion coefficient owing to the scale effect. In the four nanochannels, when the local diffusion coefficient of fluid water was in the range of 8 Å close to the wall, Dz was greater than Dxy, and beyond the range of 8 Å of the wall, the Dz was smaller than Dxy.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Parisa Jahanbakhsh Bonab ◽  
Alireza Rastkar Ebrahimzadeh ◽  
Jaber Jahanbin Sardroodi

AbstractDeep eutectic solvents (DESs) have received much attention in modern green chemistry as inexpensive and easy to handle analogous ionic liquids. This work employed molecular dynamics techniques to investigate the structure and dynamics of a DES system composed of choline chloride and phenyl propionic acid as a hydrogen bond donor and acceptor, respectively. Dynamical parameters such as mean square displacement, liquid phase self-diffusion coefficient and viscosity are calculated at the pressure of 0.1 MPa and temperatures 293, 321 and 400 K. The system size effect on the self-diffusion coefficient of DES species was also examined. Structural parameters such as liquid phase densities, hydrogen bonds, molecular dipole moment of species, and radial and spatial distribution functions (RDF and SDF) were investigated. The viscosity of the studied system was compared with the experimental values recently reported in the literature. A good agreement was observed between simulated and experimental values. The electrostatic and van der Waals nonbonding interaction energies between species were also evaluated and interpreted in terms of temperature. These investigations could play a vital role in the future development of these designer solvents.


1979 ◽  
Vol 87 (2-3) ◽  
pp. 341-344 ◽  
Author(s):  
Y. Oishi ◽  
Y. Kamei ◽  
M. Akiyama ◽  
T. Yanagi

1987 ◽  
Vol 20 (5) ◽  
pp. 1133-1141 ◽  
Author(s):  
D. S. Pearson ◽  
G. Ver Strate ◽  
E. Von Meerwall ◽  
F. C. Schilling

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