A novel solution for hydroxylated PAHs removal by oxidative coupling reaction using Mn oxide

(c) IWA Publishing 2008.

Détails bibliographiques
Publié dans:Water science and technology : a journal of the International Association on Water Pollution Research. - 1986. - 58(2008), 1 vom: 21., Seite 171-8
Auteur principal: Kang, Ki-Hoon (Auteur)
Autres auteurs: Lim, Dong-Min, Shin, Hyun-Sang
Format: Article en ligne
Langue:English
Publié: 2008
Accès à la collection:Water science and technology : a journal of the International Association on Water Pollution Research
Sujets:Journal Article Research Support, Non-U.S. Gov't Indicators and Reagents Manganese Compounds Naphthols Oxides Polycyclic Aromatic Hydrocarbons birnessite 1-naphthol 2A71EAQ389 plus... manganese oxide 64J2OA7MH3
Description
Résumé:(c) IWA Publishing 2008.
In this study, removals of 1-naphthol by oxidative-coupling reaction using birnessite, one of the natural Mn oxides present in soil, was investigated in various experimental conditions (reaction time, Mn oxide loadings, pH). The removal efficiency of 1-naphthol by birnessite was high in all the experimental conditions, and UV-visible and mass spectrometric analyses on the supernatant after reaction confirmed that the reaction products were oligomers formed by oxidative-coupling reaction. Pseudo-first order rate constants, k, for the oxidative transformation of 1-naphthol by birnessite was derived from the kinetic experiments under various amounts of birnessite loadings, and using the observed pseudo-first order rate constants with respect to birnessite loadings, the surface area normalised specific rate constant, k(surf), was also determined to be 9.3 x 10(-4) (L/m(2).min) for 1-naphthol. In addition, the oxidative transformation of 1-naphthol was found to be dependent on solution pH, and the pseudo-first order rate constants were increased from 0.129 at pH 10 to 0.187 at pH 4
Description:Date Completed 31.12.2008
Date Revised 24.11.2016
published: Print
Citation Status MEDLINE
ISSN:0273-1223
DOI:10.2166/wst.2008.637