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The behavior of triacetoneaminoxyl (TANO) and 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) in irradiated aqueous solutions in the presence of oxygen

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dc.contributor.author Anastassopoulou, JD en
dc.contributor.author Chandrinos, JD en
dc.contributor.author Rakintzis, NTh en
dc.date.accessioned 2014-03-01T01:05:59Z
dc.date.available 2014-03-01T01:05:59Z
dc.date.issued 1981 en
dc.identifier.issn 01465724 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/9105
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-49149138963&partnerID=40&md5=1ea01f9fd732e2c615aafaa99394419b en
dc.subject.classification Chemistry, Physical en
dc.subject.classification Nuclear Science & Technology en
dc.subject.classification Physics, Atomic, Molecular & Chemical en
dc.title The behavior of triacetoneaminoxyl (TANO) and 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) in irradiated aqueous solutions in the presence of oxygen en
heal.type journalArticle en
heal.language English en
heal.publicationDate 1981 en
heal.abstract The mechanism of the γ-radiolysis of the free nitroxyl radicals TANO and TEMPO in neutral aqueous solutions in the presence of oxygen has been investigated. The disappearance of TANO and TEMPO was followed by measuring the decrease in absorbance at 235 and 245 nm, respectively. The kinetic results obtained can be interpreted on the basis of competition between the nitroxyls and oxygen for the reducing radicals H and e-aq, produced in irradiated water. From this competition the rate constants for the reaction of TANO and TEMPO with the reducing radicals were determined: k(TANO + Rred) = 6.4 × 1010 and k(TEMPO + Rred) = 1.42 × 1010 M-1 sec-1, where Rred = H + e-aq. The radicals HO2 and O-2 do not attack TANO and TEMPO, at least as far as the NO group of these molecules is concerned. © 1981. en
heal.publisher PERGAMON-ELSEVIER SCIENCE LTD en
heal.journalName Radiation Physics and Chemistry en
dc.identifier.isi ISI:A1981LF03800009 en
dc.identifier.volume 17 en
dc.identifier.issue 2 en
dc.identifier.spage 119 en
dc.identifier.epage 121 en


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