Issue 9, 2019

The reactivity and pathway of Fenton reactions driven by hydroxybenzoic acids: the effect of hydroxylation

Abstract

Hydroxybenzoic acids (HBAs) are neglected as promoters of the Fenton reaction due to their low reduction capacity of Fe(III) and facile capture of hydroxyl radicals. However, autocatalysis often occurs in HBA degradation by the Fe(III)/H2O2 system. In this study, we investigated the effect of various HBA compounds on the Fenton reaction, and found that model HBAs also showed good catalytic activity. Their capability to promote the Fenton reaction is closely related to their readiness to be transformed into a hydroquinone-like (HQ-like) species. Electron-donating groups (EDGs) can accelerate the hydroxylation of aromatic compounds, thus leading to the rapid formation of a HQ-like species.

Graphical abstract: The reactivity and pathway of Fenton reactions driven by hydroxybenzoic acids: the effect of hydroxylation

Supplementary files

Article information

Article type
Paper
Submitted
23 মার্চ 2019
Accepted
23 জুলাই 2019
First published
24 জুলাই 2019

Environ. Sci.: Water Res. Technol., 2019,5, 1507-1514

The reactivity and pathway of Fenton reactions driven by hydroxybenzoic acids: the effect of hydroxylation

D. Tang, G. Zhang, Y. Wang, F. Chen and J. Ma, Environ. Sci.: Water Res. Technol., 2019, 5, 1507 DOI: 10.1039/C9EW00250B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements