A~traet--CO~ reacts in acid solutions with chemisorbed hydrogen on platinum in the potential range of Eh = 0-250 mV to form a chemisorption product of reduced COs (perhaps CO). The rate of reduction on bright platinum at room temperature is very slow, taking more than 2 min at Eh = 0 for the total
The electrochemical reduction of ruthenium(IV) in perchloric acid solutions on platinum electrodes
โ Scribed by J. Schauwers; F. Meuris; L. Heerman; W. D'Olieslager
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 611 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
Two reversible wavesare observed for the reduction of Ru(IV) on platinum electrodes. Each wave is the sum of two one-electron steps according to: 1st wllve Ru,(OH):: (IV)-Ru4(0H)$ (3,75)=Ru,(OH):+ (3.5) 2nd wave /wv-l Ru,(OH);+ (3,S)=Ru,(OH);+ (3.25)= Ru+(OH):+ (III) k, 4 stable Ru(II1) Potentials (as nhe) and species are given for 1 .O M HCIO, solutions; more hydrolyzed products are formed in less acid solutions. The tetrameric Ru(lII) ion slowly decomposes to a more stable Ru(III) species, probably a dimeric ion.
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The adsorption of formic acid was studied on smooth platinum in 1 N HClO, at 0.2 V as a function of time at different bulk concentrations of formic acid at 25". Conditions could be kept such that an appreciable amount of inte~ediates or side products were not formed. Small volumes of HCOOH were adde
The electrochemical reduction of the thick oxide film formed on Pt electrode by severe Dreanodiition has been studied in LiOH, NaOH and KOH solutions of different concentrations &lOl -1.0 M) using a galvanostatic technique. An outermost monolayer oxide and an inner multilayer oxide of the thick oxid