A physical model of bulk-nanochannel-bulk with buffer baths is built up using nonequilibrium molecular dynamics （MD） simulation to study the effects of vibrating silicon atoms on the viscosity of aqueous NaCl soluti...
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A physical model of bulk-nanochannel-bulk with buffer baths is built up using nonequilibrium molecular dynamics （MD） simulation to study the effects of vibrating silicon atoms on the viscosity of aqueous NaCl solutions confined in the nanochannel. The simulation is performed under different moving speeds of the upper wall, different heights and different surface charge densities in the nanochannel. The simulation results indicate that with the increase in the surface charge density and the decrease in the nanochannel height and the shear rate, the vibration effect of silicon atoms on the shear viscosity of the confined fluid in the nanochannel cannot be ignored. Compared with still silicon atoms, the vibrating silicon atoms result in the decrease in the viscosity when the height of the nanochannel is less than 0.8 nm and the shear rate is less than 1.0 ×10^11 s^-1, and the effect of the vibrating silicon atoms on the shear viscosity is significant when the shear rate is small. This is due to the fact that the vibrating silicon atoms weaken the interactions between the counter-ions （Na^＋ ） and the charged surface.
The forces between two molecularly smooth mica surfaces are measured in monovalent and divalent cations electrolyte solutions by a surface force apparatus （SFA）. The properties of K＋, Na＋, and Mg2＋ between molecu...
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The forces between two molecularly smooth mica surfaces are measured in monovalent and divalent cations electrolyte solutions by a surface force apparatus （SFA）. The properties of K＋, Na＋, and Mg2＋ between molecularly smooth mica surfaces are investigated. The Derjagui-Landau- Verwey-Overbeek （DLVO） force and the hydration force are detected in the experiment. The results show that in lower concentrations of a monovalent electrolyte solution （about 10-4 mol/L）, the force curves are completely in good agreement with those computed by the DLVO theory. However, additional short-range repulsive forces which deviate from the DLVO theory are observed when the concentrations of cations are above the critical bulk concentration, which is different for each electrolyte. The results show the properties of these cations on both the screening effect adsorbed on the mica surface and the hydration in solution. From the results, the interaction energy between two hydrated ions of potassium or sodium can also be estimated.
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