Electrochemical determination of acidity level and dissociation of formic acid/water mixtures as solvent

被引:30
作者
Ferrer, J. S. Jaime [1 ]
Couallier, E. [1 ]
Rakib, M. [1 ]
Durand, G. [1 ]
机构
[1] Ecole Cent Paris, Lab Genie Proc & Mat, F-92295 Chatenay Malabry, France
关键词
acidity scale; autoprotolysis constant; formic acid; formic acid/water mixtures; redox function;
D O I
10.1016/j.electacta.2007.02.058
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The autoprotolysis constant K-HS of formic acid/water mixtures as solvent has been calculated from acid-base potentiometric titration curves. A correlation of the acidity scale pK(HS) of each medium versus pure water has been implemented owing to the Strehlow R-0(H+) electrochemical redox function. The results show that formic acid/water mixtures are much more dissociated than pure water; such media are sufficiently dissociated to allow electrochemical measures without addition of an electrolyte. It has also been shown that for a same H+ concentration the activity of protons increases with formic acid concentration. For more than 80 wt.% of formic acid the acidity is sufficiently increased to locate the whole acidity scale pK(HS) in the super acid medium of the generalized acidity scale pH(H2O). (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5773 / 5780
页数:8
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