scholarly journals Energy‐Efficient Gas‐Phase Electrolysis of Hydrogen Chloride

2019 ◽  
Vol 91 (6) ◽  
pp. 795-808 ◽  
Author(s):  
Simon Bechtel ◽  
Tanja Vidaković‐Koch ◽  
Kai Sundmacher
1987 ◽  
Vol 5 (1) ◽  
Author(s):  
Roger Atkinson ◽  
SaraM. Aschmann ◽  
ErnestoC. Tuazon ◽  
MarkA. Goodman ◽  
ArthurM. Winer

2013 ◽  
Vol 78 (12) ◽  
pp. 2115-2130 ◽  
Author(s):  
Martinez Gonzalez ◽  
Tanja Vidakovic-Koch ◽  
Rafael Kuwertz ◽  
Ulrich Kunz ◽  
Thomas Turek ◽  
...  

Hydrogen chloride (HCl) oxidation has been investigated on technical membrane electrode assemblies in a cyclone flow cell. Influence of Nafion loading, temperature and hydrogen chloride mole fraction in the gas phase has been studied. The apparent kinetic parameters like reaction order with respect to HCl, Tafel slope and activation energy have been determined from polarization data. The apparent kinetic parameters suggest that the recombination of adsorbed Cl intermediate is the rate determining step.


2015 ◽  
Vol 28 (4) ◽  
pp. 261-265 ◽  
Author(s):  
Libia L. Julio ◽  
José R. Mora ◽  
Alexis Maldonado ◽  
Gabriel Chuchani

1968 ◽  
Vol 21 (3) ◽  
pp. 687 ◽  
Author(s):  
JTD Cross ◽  
VR Stimson

Hydrogen bromide and hydrogen chloride catalyse the decomposition of methyl trimethylacetate into isobutene, carbon monoxide, and methanol at 370-442� and 450-48O�, respectively. The kinetic form, which is basically 1 : 1, is severely modified by the effect of methanol either produced in the reaction or added initially. Water or alcohols react with an intermediate in the catalysed decomposition of trimethylacetic acid or its methyl ester in esterification-like reactions; some of the resultant esters subsequently decompose to olefin and acid.


1966 ◽  
Vol 19 (3) ◽  
pp. 401 ◽  
Author(s):  
VR Stimson ◽  
EJ Watson

Hydrogen chloride catalyses the decomposition of t-butyl ethyl ether at 320-428�. Isobutene is quantitatively the product and the kinetic form is first order in the ether and in hydrogen chloride. The Arrhenius equation:��������� k, = 1012'16exp( -30,60O/RT) (sec-l ml mole-=) is followed. The mechanism of the reaction seems similar to those of other hydrogen halide catalysed decompositions of ethers and alcohols.


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