Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 18, Issue 15, Pages 4699-4705Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201102671
Keywords
colloids; heterogeneous catalysis; nanoparticles; radicals; radiolysis
Categories
Funding
- Israel Atomic Energy Committee
- Planning and budgeting Committee of the Israeli Council of Higher Education
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Methyl radicals react in fast reactions, with rate constants k>1x108M-1s-1, with Au0, Ag0 and TiO2 nanoparticles (NPs) dispersed in aqueous solutions to form intermediates, (NP) (CH3)n, in which the methyl groups are covalently bound to the NPs. These intermediates decompose to form ethane. As n=2 is required for the formation of C2H6, the minimal lifetime (t) of the methyls bound to the NPs, (NP)CH3, can be estimated from the rate of production of the CH3(center dot) radicals and the NPs concentration. The results obtained in this study, using a very low dose rate gamma-source for NP=Ag0, Au0, and TiO2 point out that t of these intermediates is surprisingly long, for example, =8 and =188 sec for silver and gold, respectively. These data point out that the NPC bond dissociation energies are =70 kJmol-1. Under low rates of production of CH3., that is, when the rate of formation of ethane is very low, other reactions may occur, consequently the mechanism proposed is broken. This is observed in the present study only for TiO2 NPs. These results have to be considered whenever alkyl radicals are formed near surfaces. Furthermore, the results point out that the rate of reaction of methyl radicals with (NP)(CH3)n depends on n, that is, the number of methyl radicals bound to the NPs affect the properties of the NPs.
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