Abstract
The concentration dependence of the apparent molar volumes of lithium halides (and electrolytes in general) in alcohols (and solvents permitting association in general) is, in the first instance, due to changes in the degree of association and to the inherent difference between the apparent molar volumes of the ions and of the ion pairs. Previous publications on the molar volumes of electrolytes in organic solvents, disregarding altogether ion pairing, appear to be incorrect. Data from the literature for lithium chloride and lithium bromide in normal primary alcohols and several branched alcohols from C1 to C8 and data from our laboratory for lithium halides in 1-hexanol and 2-ethyl-1-hexanol served for the determination of φ V and φ E . Electrical and structural contributions to the values of these functions for the ions and for the ion pairs are discussed.
Original language | English |
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Pages (from-to) | 87-106 |
Number of pages | 20 |
Journal | Journal of Solution Chemistry |
Volume | 5 |
Issue number | 2 |
DOIs | |
State | Published - Feb 1976 |
Keywords
- Alcohols
- electrolytes
- electrostriction
- ion pairing
- lithium bromide
- lithium chloride
- molar expansibility
- molar volume
- nonaqueous