A COMPARISON OF THE EFFECTIVENESS OF GLUTAMIC ACID HYDROCHLORIDE AND DILUTE HYDROCHLORIC ACID AS THE REPLACEMENT THERAPY IN ANACIDITY MEASURED BY FRACTIONAL GASTRIC ACID TITRATION AND HYDROGEN-ION CONCENTRATION CURVES

1936 ◽  
Vol 9 (12) ◽  
pp. 1628 ◽  
1931 ◽  
Vol 15 (2) ◽  
pp. 119-124 ◽  
Author(s):  
William H. Cole ◽  
James B. Allison

1. The reaction of the catfish, Schilbeodes gyrinus Mitchill, to hydrochloric acid over a wide range of concentrations (from pH 1.82 to pH 6.83) has been studied under experimental conditions which reduced to a minimum all other stimuli. 2. As the [H+J increases within the limits mentioned, the reaction time of the fish decreases. In other words, the rate of the stimulation processes is an increasing function of the hydrogen ion concentration. 3. The effective stimulus is the hydrogen ion, since NaCl solutions of equivalent concentration were not stimulating. 4. Stimulation by hydrochloric acid is therefore correlated with the potential of the cation resulting from dissociation of the acid molecule.


1919 ◽  
Vol 1 (4) ◽  
pp. 459-472 ◽  
Author(s):  
L. J. Henderson ◽  
Edwin J. Cohn ◽  
P. H. Cathcart ◽  
J. D. Wachman ◽  
W. O. Fenn

In this paper there are reported studies of the acid-base equilibrium in systems containing gluten suspended in solution of hydrochloric acid and sodium hydroxide. The studies have involved measurements of the hydrogen ion concentration, of the electrical conductivity, and of the solution of the proteins. Further, measurements have been made of the swelling and of the viscosity of the gluten component of such systems. The results seem to show that simple chemical phenomena are most important in such systems, and that the modifications of these, resulting from colloidal and heterogeneous characteristics, are of secondary importance in determining the condition of equilibrium, though somewhat more significant in the progress of the system toward the condition of equilibrium.


Author(s):  
W. R. G. Atkins

It has long been known that sea water is alkaline and numerous determinations of its alkalinity have been made. The method adopted was the usual one for mixtures of carbonates and bicarbonates, or some modification of it. Those waters which give no colour with phenolphthalein contain bicarbonate only, but for the most part ocean waters have a small amount of carbonate also. Owing to the presence of larger amounts of carbonates and bicarbonates the reaction of sea water is more stable than that of rain or river water, inasmuch as it has a greater alkaline reserve which acts as a “buffer.” The significance of this has been pointed out by Moore, Prideaux, and Herdman (1915) and by other workers. The measurement of alkalinity was carried out by the above named using N/100 hydrochloric acid and titrating to the end points with phenol phthalein and methyl orange. The results are recorded in cubic centimetres of centinormal acid per 100 c.c. of sea water; this is convenient as it is what is measured directly, but others adopt the perhaps more rational notation of milligram equivalents of hydroxyl per litre (Buch, 1914). One cubic centimetre of N/100 acid per 100 c.c. corresponds to 0.1 milligram equivalent per litre. Some workers on fresh waters, Birge and Juday (1911) for example, consider water as acid if it contains more carbon dioxide than that sufficient to convert the carbonate into bicarbonate, and titrate back to a pink with phenolphthalein. Their acid water is, however, still alkaline to methyl orange.


1970 ◽  
Vol 48 (7) ◽  
pp. 1148-1150 ◽  
Author(s):  
U. S. Mehrotra ◽  
S. P. Mushran

Reduction of osmium(VIII) by ascorbic acid has been studied in the presence of hydrochloric acid. The reaction is found to be directly proportional to the concentration of ascorbic acid and osmium(VIII) and to the reciprocal of the hydrogen ion concentration. In the proposed mechanism, the reacting species have been shown to be perperosmic acid and ascorbate ion; this was supported by the negligible effect of the ionic strength. Influence of temperature was studied in the range 25–40 °C, and the energy and entropy of activation were calculated as 14.1 ± 0.2 kcal mole−1 and −8.6 ± 0.1 e.u., respectively. Osmium(IV) was found to be a product of the reaction.


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