1977
DOI: 10.1002/chin.197703030
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ChemInform Abstract: MECHANISM OF THE REDUCTION OF LEAD IONS IN AQUEOUS SOLUTION (A PULSE RADIOLYSIS STUDY)

Abstract: Bei "Co‐′y‐Bestrahlung wäßriger Pb(ClO4),‐ oder Pb(OAc),‐Lösungen fällt in Gegenwart von OH‐Radikalfängern wie Formiat, aliphatische Alkohole, Cyclopentan oder tert.‐Butanol reines Pb aus.

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Cited by 3 publications
(4 citation statements)
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“…The rate of polymerization for ZnO increases in the order acetonitrile < methanol < ethanol < isopropyl alcohol, which agrees with the redox potentials of the alcohol radicals. 40 No polymerization was observed in acetonitrile as expected, since it is not an efficient hole scavenger. The separation of the electron and the hole pair formed upon illumination is necessary for polymerization to occur.…”
Section: Resultssupporting
confidence: 53%
“…The rate of polymerization for ZnO increases in the order acetonitrile < methanol < ethanol < isopropyl alcohol, which agrees with the redox potentials of the alcohol radicals. 40 No polymerization was observed in acetonitrile as expected, since it is not an efficient hole scavenger. The separation of the electron and the hole pair formed upon illumination is necessary for polymerization to occur.…”
Section: Resultssupporting
confidence: 53%
“…The additional 2.7 silver atoms per 100 eV must have been formed under the influence of the 1-hydroxy-isopropyl radical, the main radical produced in the attack of OH in isopropanol. However, the standard redox potential of this radical [21] is not negative enough to reduce a silver ion in a simple electron transfer: (CH3)2COH + Ag' + (CH3),C0 + H + + Ago(aq). We must therefore conclude that it acts as a reductant towards either Agz or more agglomerated silver species, whose formation is initiated by the silver atom produced in the attack of ea; and H on Agt :…”
Section: (11)mentioning
confidence: 99%
“…[20] In the case of 2,3-and 2,6-DMP it was not possible to determine the rate constmts for decay of the phenoxyl radicals due to simultaneous formation of products which absorb in the same wavelength region as the phenoxyls. [21] R. Livingston and H. Zeldes, J . Amer.…”
mentioning
confidence: 99%
“…is close to -1.8 V. 4 Electron transfer from the first reduction products of thallium to Cd2+ would have little driving force; however, as in the thallium-silver system, mixed-cluster formation could be expected. The standard potential of the system Pb+ -* Pb2+ + e_ (5) is -1.0 V.5 Electron transfer from reduced thallium to lead should be strongly exoergic. The standard potential of the redox system Zn+ -* Zn2+ + eaq_ (6) is as negative as -2.5 V. 4 In this case, electron transfer from Zn+ to Tl+ seemed probable.…”
Section: Introductionmentioning
confidence: 99%