Interaction of carbon monoxide and hydrogen under silent electric discharge: Production of formaldehyde

1950 ◽  
Vol 31 (5) ◽  
pp. 317-324
Author(s):  
R. H. Sahasrabudhey ◽  
S. M. Deshpande
Keyword(s):  
Carbon Monoxide ◽  
Electric Discharge ◽  
Silent Electric Discharge

scholarly journals Silent Electric Discharge in the Equimolar Dihydrogen-Carbon Monoxide Mixture

1984 ◽  
Vol 57 (3) ◽  
pp. 869-870
Author(s):  
Sintaro Hata ◽  
Koji Hiramoto ◽  
Katsuaki Katoh ◽  
Kazuo Sasaki
Keyword(s):  
Carbon Monoxide ◽  
Electric Discharge ◽  
Silent Electric Discharge

Light paraffin oxidative conversion in a silent electric discharge

1993 ◽  
Vol 13 (3) ◽  
pp. 479-488 ◽  
Author(s):  
S. S. Shepelev ◽  
H. D. Gesser ◽  
N. R. Hunter
Keyword(s):  
Electric Discharge ◽  
Oxidative Conversion ◽  
Silent Electric Discharge

The Conversion of Silane to Higher Silanes in a Silent Electric Discharge

1962 ◽  
Vol 1 (2) ◽  
pp. 432-433 ◽  
Author(s):  
Edward J. Spanier ◽  
Alan G. MacDiarmid
Keyword(s):  
Electric Discharge ◽  
Silent Electric Discharge

scholarly journals On the gaseous condensable compound, explosive at low temperatures, produced from carbon disulphide vapour by the action of the silent electric discharge.—II

1911 ◽  
Vol 85 (582) ◽  
pp. 574-588 ◽  
Keyword(s):  
Electric Discharge ◽  
Chemical Interaction ◽  
Carbon Disulphide ◽  
Ultra Violet ◽  
Polymeric Form ◽  
Nickel Carbonyl ◽  
Ultra Violet Radiation ◽  
Gaseous Substance ◽  
Rapid Current ◽  
Silent Electric Discharge

In a former Note communicated to the Society we described the change of a rapid current of carbon disulphide vapour at a low pressure, under the influence of the silent electric discharge or of the ultra-violet radiation associated with it, into sulphur and a gaseous substance, condensable and explosive near the temperature of liquid air, forming a brown solid, resembling the polymeric form of carbon monosulphide previously obtained by the chemical interaction of thiophosgene and nickel carbonyl. This gaseous condensed substance will be called hereafter the ozoniser product. The present paper contains an account of the further study of this change and of the product obtained.

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