The Formation of Hydrogen Peroxide in the Electrodeless Discharge in Water Vapor

1936 ◽  
Vol 4 (4) ◽  
pp. 293-293 ◽  
Author(s):  
R. W. Campbell ◽  
W. H. Rodebush
1970 ◽  
Vol 48 (13) ◽  
pp. 2042-2046 ◽  
Author(s):  
Paul E. Brunet ◽  
Xavier Deglise ◽  
Paul A. Giguère

Surface effects in the reactions of dissociated hydrogen–oxygen systems and the products condensed therefrom have been investigated. Water vapor at about 0.1 Torr was streamed at high velocity through an electrodeless discharge confined in tubes of different materials or with various surface coatings. In all cases the products trapped in liquid nitrogen evolved oxygen gas on warming, but the relative amounts varied considerably from one type of surface to another. In some cases there was clear evidence that the walls of discharge tube were attacked by hydrogen atom bombardment. The decomposition, both thermal and electrical, of pure hydrogen peroxide vapor was studied likewise. The pyrolysis products gave off very little oxygen on warming. By contrast the products from electrical decomposition, even at low power level, evolved much oxygen, most of it above the melting point.It is concluded that there is always some decomposition of hydrogen peroxide in the trapped products. However, this does not seem sufficient to account for all the evolved oxygen; at least not in the case of dissociated water vapor.


1966 ◽  
Vol 44 (8) ◽  
pp. 869-876 ◽  
Author(s):  
Norisuke H Ata ◽  
Paul A. Glguère

Hydrogen gas partly dissociated in an electrodeless discharge was mixed downstream with hydrogen peroxide vapor at low pressure (0.1 mm Hg) in a liquid nitrogen trap. The reaction products condensed readily on the wall as a clear, yellowish glass resembling that from dissociated water vapor and other related systems. A manometric study of the warming-up process has revealed four distinct steps. The first two, in which only traces of gas are given off, look like the recombination of trapped free radicals. The major evolution of oxygen upon crystallization of the glassy deposit at 160 °K is ascribed to the decomposition of hydrogen peroxide under the influence of some unidentified species generated in the electric discharge through hydrogen. Experimental evidence for this is presented. In any case the stoichiometry cannot be reconciled with the formation of a metastable intermediate, such as the hypothetical polyoxide H2O4.In the last step beginning around 215 °K more peroxide is decomposed during the eutectic melting of the solid. Qualitatively these phenomena are similar to those shown by the condensate from dissociated water vapor.


1951 ◽  
Vol 29 (11) ◽  
pp. 996-1009 ◽  
Author(s):  
R. A. Jones ◽  
C. A. Winkler

Water vapor dissociated by an electric discharge and passed into a cold trap yielded products which gave off oxygen at temperatures above −120°C. and at room temperature consisted of hydrogen peroxide and water. With products formed under given conditions, the amount of oxygen evolved with warming was proportional to the total amount of product and independent of the warming procedure. The evolution proceeded to completion at −78°C. Water was found at all trap temperatures between −78°C. and −195°C. Hydrogen peroxide was formed only if the trap temperature was below −120°C., and oxygen was evolved only from products formed below −150°C. The yields of water, hydrogen peroxide, and evolved oxygen all increased with decreasing trap temperature. As the volume of reaction chambers inserted between the discharge tube and the trap was increased, the yield of hydrogen peroxide decreased continuously, while the yield of water at first decreased and then increased to a limiting value. Packing a given reaction chamber with glass wool drastically reduced the yield of hydrogen peroxide, but had little effect on the yield of water. Packing the trap itself had only a slight effect on the yields. The results are compared with those obtained by others with the H–O2 system at low temperatures, and a mechanism is proposed to correlate the two systems.


2021 ◽  
Vol 11 ◽  
Author(s):  
Editorial Office ROS

The latest cutting-edge research findings published in highly influential journals have greatly advanced our current understanding of hydrogen peroxide (H₂O₂), a notable reactive oxygen species, in chemistry, biology, and medicine. In this context, recent studies by J.K. Lee et al., published in Proc Natl Acad Sci USA, discovered a novel mechanism of spontaneous production of H₂O₂ from pure water in the absence of catalysts or external electric field. This discovery by J.K. Lee et al. has changed our view on the chemical connection between H₂O₂ and H₂O though the biological significance of the discovery remains unknown. REFERENCES Hopkins RZ, Li YR. Essentials of Free Radical Biology and Medicine. Cell Med Press, Raleigh, NC, USA. 2017. Hopkins RZ. Hydrogen peroxide in biology and medicine: an overview. React Oxyg Species (Apex) 2017; 3(7):26–37. doi: https://dx.doi.org/10.20455/ros.2017.809. Bergman P, Parise B, Liseau R, Larsson B, Olofsson H, Menten KM, et al. Detection of interstellar hydrogen peroxide. Astronomy Astrophysics 2011; 531:L8. doi: https://dx.doi.org/10.1051/0004-6361/201117170. Lee JK, Walker KL, Han HS, Kang J, Prinz FB, Waymouth RM, et al. Spontaneous generation of hydrogen peroxide from aqueous microdroplets. Proc Natl Acad Sci USA 2019; 116(39):19294‒8. doi: https://dx.doi.org/10.1073/pnas.1911883116. Lee JK, Han HS, Chaikasetsin S, Marron DP, Waymouth RM, Prinz FB, et al. Condensing water vapor to droplets generates hydrogen peroxide. Proc Natl Acad Sci USA 2020; 117(49):30934‒41. doi: https://dx.doi.org/10.1073/pnas.2020158117.


2006 ◽  
Vol 80 (12) ◽  
pp. 1999-2001
Author(s):  
G. L. Grigoryan ◽  
L. G. Tadevosyan ◽  
P. S. Gukasyan

1968 ◽  
Vol 46 (16) ◽  
pp. 2649-2653 ◽  
Author(s):  
Kazimiera Herman ◽  
Paul A. Giguère

We have reinvestigated in detail the infrared spectra between 4000 and 600 cm−1 of the solid products formed by reacting liquid ozone at −190 °C with a stream of hydrogen gas dissociated in an electrodeless discharge. Extreme care was exercised to get "clean" spectra, free from any contaminants. All the spectra thus obtained showed very clearly the characteristic absorption bands of H2O2 at 2840 and 1430 cm−1, and the much weaker one at 880 cm−1; with deuterium atoms the former bands were shifted to 2100 and 1080 cm−1 respectively. Thus previous contentions that hydrogen peroxide is not one of the primary products of that reaction are disproved. The other infrared bands of H2O2 were not conspicuous, due either to their diffuse nature in the vitreous spectra or to extensive overlapping by the strong absorption of H2O, the other major component. Warming the material up to −110 °C caused some devitrification, but no significant change in the spectra. No new bands which could be assigned unambiguously to the hypothetical molecule H2O4 were observed.


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