dc.contributor.author |
Kormali, P |
en |
dc.contributor.author |
Triantis, T |
en |
dc.contributor.author |
Dimotikali, D |
en |
dc.contributor.author |
Hiskia, A |
en |
dc.contributor.author |
Papaconstantinou, E |
en |
dc.date.accessioned |
2014-03-01T01:24:48Z |
|
dc.date.available |
2014-03-01T01:24:48Z |
|
dc.date.issued |
2006 |
en |
dc.identifier.issn |
0926-3373 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/17439 |
|
dc.subject |
Holes |
en |
dc.subject |
OH radicals |
en |
dc.subject |
Photocatalysis |
en |
dc.subject |
Polyoxometallates |
en |
dc.subject |
TiO2 |
en |
dc.subject.classification |
Chemistry, Physical |
en |
dc.subject.classification |
Engineering, Environmental |
en |
dc.subject.classification |
Engineering, Chemical |
en |
dc.subject.other |
OH radical scavengers |
en |
dc.subject.other |
Polyoxometallates |
en |
dc.subject.other |
Catalysts |
en |
dc.subject.other |
Halogen compounds |
en |
dc.subject.other |
Hole traps |
en |
dc.subject.other |
Photocatalysis |
en |
dc.subject.other |
Photooxidation |
en |
dc.subject.other |
Substrates |
en |
dc.subject.other |
Titanium dioxide |
en |
dc.title |
On the photooxidative behavior of TiO2 and PW12O403-: OH radicals versus holes |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/j.apcatb.2006.07.024 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/j.apcatb.2006.07.024 |
en |
heal.language |
English |
en |
heal.publicationDate |
2006 |
en |
heal.abstract |
Parallel experiments under similar conditions, using various substrates (atrazine, fenitrothion, 4-chlorophenol and 2,4-D) and OH radical scavengers (Br-, isopropyl alcohol, tertiary butyl alcohol and acetone), have shown that the photooxidizing mode of PW12O403- and TiO2, i.e., OH radicals and/or holes (h(+)), depends on the nature of substrate and the mode of investigation. This provides an explanation for the controversial results reported in the literature. Atrazine shows that both PW12O403- and TiO2 operate, mainly, via OH radicals and to a lesser extent with holes (h(+)), whereas, fenitrothion suggests that both systems operate almost exclusively, via OH radicals. Differences in the action of the catalysts are encountered in the photodegradation of 4-chlorophenol (4-ClPh) and 2,4-dichlorophenoxyacetic acid (2,4-D). PW12O403- appears to operate essentially via OH radicals, whereas, h(+) appear to be the major oxidant with TiO2. Overall, though, the action of OH radicals relative to h(+) appears to be more pronounced with PW12O403- than TiO2. (c) 2006 Elsevier B.V. All rights reserved. |
en |
heal.publisher |
ELSEVIER SCIENCE BV |
en |
heal.journalName |
Applied Catalysis B: Environmental |
en |
dc.identifier.doi |
10.1016/j.apcatb.2006.07.024 |
en |
dc.identifier.isi |
ISI:000241707700007 |
en |
dc.identifier.volume |
68 |
en |
dc.identifier.issue |
3-4 |
en |
dc.identifier.spage |
139 |
en |
dc.identifier.epage |
146 |
en |