4.8 Article

Isotopically labeled ozone: A new approach to elucidate the formation of ozonation products

Journal

WATER RESEARCH
Volume 233, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2023.119740

Keywords

Ozonation products; Oxygen-18; Isotope labeling; Wastewater

Ask authors/readers for more resources

As ozonation becomes a widespread treatment for removal of chemicals of emerging concern from wastewater treatment plant effluents, there are increasing concerns regarding the formation of ozonation products (OPs) and their potential impacts on the aquatic environment and human health. This study developed a new method using heavy oxygen (18O2) to label OPs from oxygen transfer reactions, and successfully confirmed the formation pathways of OPs from sulfameth-oxazole. The results provide insights into the mechanisms of ozonation and the potential to monitor and understand the formation of OPs in wastewater treatment processes.
As ozonation becomes a widespread treatment for removal of chemicals of emerging concern from wastewater treatment plant effluents, there are increasing concerns regarding the formation of ozonation products (OPs), and their possible impacts on the aquatic environment and eventually human health. In this study, a novel method was developed that utilizes heavy oxygen (18O2) for the production of heavy ozone ([18O11O2, [18O21O1, [18O31) to actively label OPs from oxygen transfer reactions. To establish and validate this new approach, venlafaxine with a well-described oxygen transfer reaction (tertiary amine -> N -oxide) was chosen as a model compound. Observed 18O/16O ratios in the major OP venlafaxine N -oxide (NOV) correlated with expected 18O purities based on tracer experiments. These results confirmed the successful labeling with heavy oxygen and furthermore demonstrate the potential to monitor NOV as an indicator of 18O/16O ratios during ozonation. As a next step, 18O/16O ratios were used to elucidate the formation mechanism of previously described OPs from sulfameth-oxazole (SMX). Seven OPs were detected including the frequently described nitro-SMX, which was formed with a maximum yield of 3.2% (of initial SMX). With the successful labeling of six of the seven OPs from sulfameth-oxazole, it was possible to confirm their previously proposed formation pathways, and to distinguish oxygen transfer from electron transfer reactions. 18O/16O ratios in OPs indicate that hydroxylation of the aromatic ring and formation of nitro-groups mostly follows oxygen transfer reactions, while electron transfer reactions initiate the formation of hydroxylamine and the abstraction of NH2 leading to catechol.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available