dc.contributor.author |
Grigoropoulou, H |
en |
dc.contributor.author |
Philippopoulos, C |
en |
dc.date.accessioned |
2014-03-01T02:41:28Z |
|
dc.date.available |
2014-03-01T02:41:28Z |
|
dc.date.issued |
1997 |
en |
dc.identifier.issn |
0273-1223 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/30475 |
|
dc.subject |
Ferric catalyst |
en |
dc.subject |
Hydrogen peroxide |
en |
dc.subject |
Phenols oxidation |
en |
dc.subject.classification |
Engineering, Environmental |
en |
dc.subject.classification |
Environmental Sciences |
en |
dc.subject.classification |
Water Resources |
en |
dc.subject.other |
Biodegradation |
en |
dc.subject.other |
Catalysts |
en |
dc.subject.other |
Chlorine compounds |
en |
dc.subject.other |
Composition effects |
en |
dc.subject.other |
Hydrogen peroxide |
en |
dc.subject.other |
Iron compounds |
en |
dc.subject.other |
Phenols |
en |
dc.subject.other |
Solutions |
en |
dc.subject.other |
Chlorophenols |
en |
dc.subject.other |
Ferric chloride |
en |
dc.subject.other |
Ferrous ammonium sulfate |
en |
dc.subject.other |
Iron sulfate |
en |
dc.subject.other |
Oxidation |
en |
dc.subject.other |
2,4,6 trichlorophenol |
en |
dc.subject.other |
ammonium sulfate |
en |
dc.subject.other |
chlorophenol |
en |
dc.subject.other |
ferric chloride |
en |
dc.subject.other |
ferric ion |
en |
dc.subject.other |
ferric sulfate |
en |
dc.subject.other |
ferrous sulfate |
en |
dc.subject.other |
hydrogen peroxide |
en |
dc.subject.other |
oxidizing agent |
en |
dc.subject.other |
phenol |
en |
dc.subject.other |
aqueous solution |
en |
dc.subject.other |
biodegradation |
en |
dc.subject.other |
catalyst |
en |
dc.subject.other |
conference paper |
en |
dc.subject.other |
environmental temperature |
en |
dc.subject.other |
oxidation |
en |
dc.subject.other |
oxygen consumption |
en |
dc.subject.other |
ph |
en |
dc.subject.other |
waste water management |
en |
dc.title |
Homogeneous oxidation of phenols in aqueous solution with hydrogen peroxide and ferric ions |
en |
heal.type |
conferenceItem |
en |
heal.identifier.primary |
10.1016/S0273-1223(97)00382-X |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/S0273-1223(97)00382-X |
en |
heal.language |
English |
en |
heal.publicationDate |
1997 |
en |
heal.abstract |
The chemical oxidation of phenol and chlorophenols with hydrogen peroxide in the presence of soluble iron can be economically attractive at low oxidant consumption, leading then to intermediates that are more easily biodegradable. The homogeneous oxidation of phenol and chlorophenols in aqueous solutions with hydrogen peroxide is studied at oxidant:phenol ratio of about 4:1 and 16:1 (mol/mol) at various catalyst concentrations, at ambient temperature without pH control. Ferric choride, ferric and ferrous sulphate and ferrous ammonium sulphate are used as oxidation catalysts. Ferric salts induce higher oxidation rates than ferrous ones and the nature of the anions present does not affect reaction rate. 4-Chlorophenol is found to be most resistant to oxidation and 2,4,6-Trichlorophenol is not attacked by hydrogen peroxide in the presence of ferric ions at the experimental conditions studied.The chemical oxidation of phenol and chlorophenols with hydrogen peroxide in the presence of soluble iron can be economically attractive at low oxidant consumption, leading then to intermediates that are more easily biodegradable. The homogeneous oxidation of phenol and chlorophenols in aqueous solutions with hydrogen peroxide is studied at oxidant : phenol ratio of about 4:1 and 16:1 (mol/mol) at various catalyst concentrations, at ambient temperature without pH control. Ferric chloride, ferric and ferrous sulphate and ferrous ammonium sulphate are used as oxidation catalysts. Ferric salts induce higher oxidation rates than ferrous ones and the nature of the anions present does not affect reaction rate. 4-Chlorophenol is found to be most resistant to oxidation and 2,4,6-Trichlorophenol is not attacked by hydrogen peroxide in the presence of ferric ions at the experimental conditions studied. |
en |
heal.publisher |
Elsevier Science Ltd, Oxford, United Kingdom |
en |
heal.journalName |
Water Science and Technology |
en |
dc.identifier.doi |
10.1016/S0273-1223(97)00382-X |
en |
dc.identifier.isi |
ISI:A1997YG15000020 |
en |
dc.identifier.volume |
36 |
en |
dc.identifier.issue |
2-3 |
en |
dc.identifier.spage |
151 |
en |
dc.identifier.epage |
154 |
en |