scholarly journals The second dissociation constant of p-phenolsulfonic acid and pH values of phenolsulfonate-chloride buffers from 0 degrees to 60 degrees C

1943 ◽  
Vol 31 (4) ◽  
pp. 205 ◽  
Author(s):  
R.G. Bates ◽  
G.L. Siegel ◽  
S.F. Acree
1974 ◽  
Vol 143 (3) ◽  
pp. 775-777 ◽  
Author(s):  
John L. Wood

The pH-dependence of the degree of hydrogen-bonding between a base and its conjugate acid is considered. When only a small proportion of the total base is complexed, the amount complexed is proportional to (1+coshp)−1 where p=2.303 (pKa–pH), pKa being the dissociation constant of the conjugate acid. This represents sharp pH-dependence. As the proportion complexed increases, the curve broadens, eventually becoming flat-topped, with more than half the base complexed over the range of pH values pKa±logKC, approximately. (K is the complex association constant and C is the formal base concentration, including all forms.) There are similarities to the extent of mono-protonation of a dibasic acid.


1993 ◽  
Vol 65 (8) ◽  
pp. 1084-1087 ◽  
Author(s):  
Y. C. Wu ◽  
P. A. Berezansky ◽  
Daming. Feng ◽  
W. F. Koch

2019 ◽  
Vol 57 (8) ◽  
pp. 745-750
Author(s):  
İlkay Konçe ◽  
Ebru Çubuk Demiralay ◽  
Hülya Yılmaz Ortak

Abstract The presented study describes the development of reversed-phase liquid chromatography method using a core-shell particle column with a pentafluorophenyl stationary phase for the dissociation constant (pKa) determination of the tetracycline group antibiotics (tetracycline, oxytetracycline, chlortetracycline) and their epimers (4-epitetracycline, 4-epioxytetracycline, 4-epichlortetracycline). The pH values were measured in the acetonitrile (ACN)–water binary mixtures, used as mobile phases, instead of in water and take into account the effect of the activity coefficients. Thermodynamic acid dissociation constant (pKa1) values of studied antibiotics and their epimers were calculated using retention factor (k) at different mobile phase pH values in studied binary mixtures with ACN percentages of 20, 25, 30 and 35% (v/v). Experimental data were analyzed by using an Origin 7.0 program to fit experimental data to the nonlinear expression derived. From calculated pKa1 values, the aqueous pKa values of studied compounds were calculated by different approaches and these values were compared.


1994 ◽  
Vol 23 (1) ◽  
pp. 75-80 ◽  
Author(s):  
P. Luts ◽  
J. Vanhees ◽  
J. Yperman ◽  
J. Mullens ◽  
L. C. Van Poucke

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