Study of Lithium Solvation Environments in Water-saturated Nitrobenzene

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Please use this identifier to cite or link to this item: http://hdl.handle.net/1853/14105

Title: Study of Lithium Solvation Environments in Water-saturated Nitrobenzene
Author: Moakes, Greg
Abstract: It was found that there exist three major water environments when water is dissolved in nitrobenzene. 2H NMR has proved that these solvatomers exist irrespective of whether lithium salt is added to the system. 7Li NMR experiments suggested that the first solvatomer is majority nitrobenzene, the second a mixed solvation shell consisting of nitrobenzene and water and the third solvatomer is a large water aggregated at the glass surface. The mixed solvation state is short lived and is promoted by addition of water of by supersaturating the system upon cooling. This is a high energy state and decays either into the homogenous bulk NB state or to the surface of the glass wall, depending on if glass surface is present. In the 7Li NMR experiments, the hydrophobicity of the salt, determined by the anion, affects the relative intensity of the three 7Li resonances. Addition of lithium serves to promote hydrogen bonding in the majority nitrobenzene solvatomer, as confirmed by FTIR and neutron diffraction studies. There is no evidence that it has an effect on the size of the mixed solvatomer or the water aggregate immobilized on the glass surface. A reasonable hypothesis is that lithium exchanges between the water species which are formed independent of lithium involvement. The system is summarized as follows: Below critical water concentration (~200mM) nitrobenzene/water is a homogeneous distribution of water molecules in nitrobenzene. Addition of lithium salt to such a system has two main affects. First, the lithium promotes hydrogen bonding between the dissolved water molecules, as confirmed by FTIR and neutron scattering. Second, the hydrogen bonded water may precipitate causing microheterogeneity of the system, leading to a second resonance observed in both the 2H and 7Li NMR spectra (LiNB/W). In the presence of glass, a third solvation state can nucleate at the glass surface; this solvation state has character even closer to that of bulk water (LiW). These two supplementary solvation states can be artificially induced by either adding aliquots of water or cooling.
Type: Dissertation
URI: http://hdl.handle.net/1853/14105
Date: 2006-11-14
Publisher: Georgia Institute of Technology
Subject: Electrochemistry
Liquid-liquid interface
Solvation
FTIR
NMR
ITIES
Solution (Chemistry)
Surface chemistry
Lithium silicates
Nitrobenzene
Solvation
Electrochemistry
Interfaces (Physical sciences)
Department: Chemistry and Biochemistry
Advisor: Committee Chair: Janata, Jiri; Committee Member: Bottomley, Lawrence; Committee Member: Eckert, Charles; Committee Member: Gelbaum, Leslie; Committee Member: Lyon, Louis Andrew
Degree: Ph.D.

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