Abstract
The observed external transverse magnetic field effect on electrolyte diffusion in diamagnetic alkali chloride (LiCl, NaCl; KCl and CsCl)-water solutions, expressed as the fractional arithmetic average integral diffusion coefficient, D *=[(⪡ D 0 H > -< D 0 > )/< D 0 > ;]×10 2; has been correlated with structural (hydration number, viscosity and ionic limiting equivalent conductance) and microdynamical (proton nuclear magnetic relaxation times and proton nuclear magnetic resonance shifts) parameters expressing the configurational rearrangement modes of the solvent and solute molecules forming the aqueous solution.
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