4.8 Article

Thiourea Dioxide Coupled with Trace Cu(II): An Effective Process for the Reductive Degradation of Diatrizoate

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 17, Pages 12009-12018

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c03823

Keywords

diatrizoate; refractory X-ray contrast media compounds; thiourea dioxide; trace concentrations of copper; Cu(I) complexes; deiodination; reduction reaction; hospital wastewater

Funding

  1. Natural Science Foundation [52070188]
  2. Zhejiang Provincial Natural Science Foundation of China [LY20B070003]

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The coupling reaction of thiourea dioxide with trace copper ions can efficiently degrade refractory Diatrizoate, achieving deiodination and degradation at neutral pH values. In this process, copper(I) ions play a key role, and increasing the thiourea dioxide dosage and extending the reaction time can improve the degradation efficiency.
Diatrizoate, a refractory ionic iodinated X-ray contrast media (ICM) compound, cannot be efficiently degraded in a complex wastewater matrix even by advanced oxidation processes. We report in this research that a homogeneous process, thiourea dioxide (TDO) coupled with trace Cu(II) (several micromoles, ubiquitous in some wastewater), is effective for reductive deiodination and degradation of diatrizoate at neutral pH values. Specifically, the molar ratio of iodide released to TDO consumed reached 2 under ideal experimental conditions. TDO eventually decomposed into urea and sulfite/sulfate. Based on the results of diatrizoate degradation, TDO decomposition, and Cu(I) generation and consumption during the TDO-Cu(II) reaction, we confirmed that Cu(I) is responsible for diatrizoate degradation. However, free Cu(I) alone did not work. It was proposed that Cu(I) complexes are actual reactive species toward diatrizoate. Inorganic anions and effluent organic matter negatively influence diatrizoate degradation, but by increasing the TDO dosage, as well as extending the reaction time, its degradation efficiency can still be guaranteed for real hospital wastewater. This reduction reaction could be potentially useful for in situ deiodination and degradation of diatrizoate in hospital wastewater before discharge into municipal sewage networks.

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