144
Views
13
CrossRef citations to date
0
Altmetric
Original Articles

Light-induced transformations of fungicides on titanium dioxide: pathways and by-products evaluation using the LC-MS technique

, , &
Pages 265-275 | Received 27 Sep 2004, Accepted 06 May 2005, Published online: 20 Aug 2006
 

Abstract

Azoxystrobin, carbendazim, and mepanipyrim, widely used heterocyclic fungicides, have been photocatalytically degraded in aqueous solution on TiO2. Several concomitant pathways occur, concerning reductive and/or oxidative attacks, thus leading to numerous intermediates, identified and characterized through an MS n spectra analysis. Multiple stage mass spectrometry of redox degradation compounds was simpler than that of parent fungicides, whose strong structures sometimes caused deactivated fragmentation pathways. Noteworthy were the different fragmentation ways that enabled hydroxylation positions to be located. Azoxystrobin is easily degraded and, within a few hours of irradiation, complete mineralization is achieved. For mepanipyrim and carbendazim, instead of an initial marked degradation, a lack in both carbon and nitrogen mineralization is observed. This is linked to the formation in both cases of guanidine, the only species persistently observed in the investigated time and still containing bound nitrogen.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 1,223.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.