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   <subfield code="a">Conductance of the hydroxide ion in tert -butyl alcohol-water and 1,4-dioxane-water mixtures</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Yuichiro Tada, Kazuyasu Ibuki, Noriaki Tsuchihashi, Masakatsu Ueno]</subfield>
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   <subfield code="a">Limiting molar conductances λo of potassium hydroxide in 2 to 25 mol%tert-butyl alcohol (TBA)-water mixtures were determined at 25°C as a function of pressure up to 196 MPa. λo's of KOH in (2.5 to 15 mol%) 1,4-dioxane-water mixtures at 25°C and 1 atm were also determined. The excess conductance λ o e of the OH- ion estimated as [λ o e (OH-) = λo(KOH) - λo(KCl)] decreased with an increase in the TBA or dioxane content, as did the excess proton conductance λ o e (H+) [λ o e (H+) = λO(HC1) - λo(KCl)]. Although λ o e (OH-) is smaller than λ o e (H+) at all solvent compositions studied, the rate of decrease in λ o e with organic content is larger for the OH- ion than for the H3O+ ion in both solvent mixtures except in the water-rich region of TBA-water mixtures. λ o e (OH-) increases with pressure more strongly in TBA-water mixtures than in pure water, and the rate of increase in λ o e (OH-) with pressure has a maximum at 5 mol% of TBA. These results are discussed in terms of the difference in stability of hydrogen bonds between the OH- or the H3O+ ion and water molecules and the increase in repulsive forces due to the orientation [H-O O-H] of water molecules in the mixtures.</subfield>
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