scholarly journals IV. The conditions of chemical change between nitric acid and certain metals

1891 ◽  
Vol 48 (292-295) ◽  
pp. 458-459 ◽  

This paper is in continuation of a preliminary communication on the same subject; the main points contained in it are as follows: I. The metals copper, mercury, and bismuth do not dissolve in nitric acid of about 30 per cent, concentration (the acid commonly employed for the preparation of nitric oxide gas) and heated to a temperature of 30ºC., provided that nitrous acid is neither present initially nor formed subsequently. To prevent this, it is nocessary in the cases of copper and bismuth to add a small quantity of some oxidising substance, such as hydrogen peroxide or potassium chlorate, or, as less efficacious, potassium permanganate, or to pass a current of air or, lastly, such a substance as urea, which destroys the nitrous acid by its interaction.

2019 ◽  
Vol 48 (37) ◽  
pp. 13916-13920 ◽  
Author(s):  
Mohammed Ajmal Puthiyaveetil Yoosaf ◽  
Somnath Ghosh ◽  
Yatheesh Narayan ◽  
Munendra Yadav ◽  
Subash Chandra Sahoo ◽  
...  

Here, we report a new pathway for nitrite reduction chemistry, formation of cobalt-nitrosyl ({CoII-NO}8) with H2O2 in the reaction of a CoII-nitrito complex with a one-fold acid (H+) via the formation of a CoII-nitrous acid intermediate ({CoII-ONOH}).


The experiments described by one of us in another paper have established that the necessary condition for the chemical reactions between nitric acid and the metals copper, mercury, and bismuth, is the presence and continuous formation of nitrous acid. These results confirm the previous observations of Russell in the case of the metal silver. Further, it has been shown that when these metals are introduced into purified nitric acid, no apparent change takes place at first, but after some time gas bubbles are seen to rise from the surface of the metal, and the liquid then contains an amount of nitrous acid which can be detected by the more delicate reagents. The amount of this acid increases up to a maximum and constant point, while concomitantly the amount of metal dissolved per unit of time equally increases to a maximum and constant value. It seemed, therefore, desirable to ascertain if these phenomena determined by the balance are correlated with any alteration of electromotive force. To avoid any misunderstanding, however, it would be advisable at the outset to state that this paper is separated from that of one of us “On the Condition of Chemical Change between certain Metals and Nitric Acid,” rather on account of division of labour than of difference of subject. The idea of measuring the electromotive force of cells consisting of platinum, certain metals, and nitric acid occurred to the latter of us, while the apparatus and method of measurement finally adopted are due solely to the former. Previous Investigations . Many years ago Faraday pointed out that neither nitrogen peroxide nor nitric acid are conductors when pure, but that the addition of water to the former, or of nitrous acid to the latter, produces the property of conductivity “in a very high degree among electrolytes.” Thus the presence of nitrous acid is the necessary condition that nitric acid should become an electrolyte. Again, Faraday proved that the electric position of certain pairs of metals in nitric acid is varied according to the conditions of concentration and temperature; in fact, experiments on this point were considered by him to be of especial importance in confirming the chemical and disproving the contact theory of the voltaic cell.


The science of chemistry presents few problems at once of such technical importance and such almost infinite complexity as the transformations of nitric acid; few problems, therefore, have been studied with so much diligence by a number of investigators. The preparation of certain metallic nitrates, the chemical changes and correlated electromotive forces of certain forms of batteries, require but to be mentioned, while the preparation of nitric oxide gas from metallic copper and moderately concentrated nitric acid forms both an exercise set before the veriest tyro in chemistry and the subject of several extensive memoirs. Within the last ten years no investigations have attracted so much attention as those which have proved beyond doubt that chemical changes hither6to regarded as almost fundamental, and as occurring between two substances, whether elementary or compound, do not in reality take place except in presence of some third substance. Thus, Dixon has shown that carbonic oxide will not combine with oxygen; H. B. Baker, that sulphur, phosphorus, and carbon do not burn in oxygen; Wanklyn, as also Cowper, that certain metals will not burn in chlorine; and other results might also be enumerated. In all these cases the necessary tertium quid is water.


1911 ◽  
Vol 33 (3) ◽  
pp. 292-299 ◽  
Author(s):  
Gilbert N. Lewis ◽  
Arthur Edgar

1973 ◽  
Vol 26 (7) ◽  
pp. 1607 ◽  
Author(s):  
PK Bhattacharyya ◽  
RD Saini

On the basis of the competitive reaction of nitrous acid with hydrogen peroxide in nitric acid medium the rate constant of the reaction of 4- aminobenzenesulphonamide with nitrous acid has been determined to be 6.4 l2 mol-2 s-1 at 22�C and has been found to be independent of nitric acid concentration in the range 0.5-2M.


1859 ◽  
Vol 9 ◽  
pp. 594-597 ◽  

Piria’s important discovery that the action of nitrous acid upon asparagin gives rise to the formation of malic acid, has led to a very general application of this agent in the study of nitrogenous substances. The results obtained have been almost always analogous to those produced by Piria; the reaction may be illustrated by the following examples:— The plan hitherto adopted consisted in submitting the aqueous solution of the nitrogenous body directly to the action of nitrous acid, or in dissolving the body in nitric acid, and passing into the solution a current of binoxide of nitrogen. By employing alcoholic and ethereal solutions, I have arrived at different results, establishing a new mode of reaction ; of the facts which I have observed the following may be quoted as illustrations.


1967 ◽  
Vol 45 (19) ◽  
pp. 2177-2190 ◽  
Author(s):  
P. de Mayo ◽  
J. J. Ryan

The structure of isamic acid, prepared by the reaction of isatin with ammonia, has been established. It is that of the ylid XIIa or XIIc, different from the ylid XIIb first suggested by the present authors in an earlier communication. The difference lies in an unsuspected exchange of nitrogen functions.The nature of the oxidation products with hydrogen peroxide (VII), with nitric acid, and with potassium permanganate (XXVII) has been elucidated; these do not differ from those suggested earlier.In the Appendix the action of diazomethane on N-acetyl isatoic acid is described. Three molecules of reagent are consumed in esterification, homologation, and epoxide formation.


CORROSION ◽  
1958 ◽  
Vol 14 (1) ◽  
pp. 27-30
Author(s):  
W. P. McKINNELL ◽  
L. F. LOCKWOOD ◽  
R. SPEISER ◽  
F. H. BECK ◽  
M. G. FONTANA

Abstract Earlier work by other investigators has shown that nitrous acid is involved in the passivation of iron in concentrated nitric acid solutions. This paper describes the effect of nitric oxide, HNO2 and HNO3 on the corrosion of active Type 302 stainless steel by 10 percent H2SO4. Specimens of Type 302 stainless steel, activated by abrading on 240 grit emery cloth and exposed to 10 percent H2SO4 solutions, were passivated by bubbling nitric oxide through the solution. Bubbling oxygen through the solution did not passivate these abraded specimens. Abraded specimens exposed to an atmosphere of nitric oxide before immersion in nitric oxide-free H2SO4 remained active. Spot tests of 10 percent H2SO4 treated with nitric oxide revealed the presence of nitrite and nitrate ions in the solution. The addition of one part of 10 percent HNO3 to 60 parts of 10 percent H2SO4 was found to produce passivity of abraded stainless steel specimens exposed to the solution. 4.3.2


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