AI Article Synopsis

  • The study explores the use of Ru(III) ions to activate periodate (PI) for the effective oxidation of trace organic pollutants, specifically carbamazepine (CBZ), across a wide pH range (3.0-11.0).
  • The Ru(III)/PI system outperforms other transition and noble metal ion systems in terms of oxidation efficiency, due to the dominance of high-valent Ru-oxo species (Ru(V)=O) as the primary oxidant.
  • This advanced oxidation process demonstrates nearly 100% utilization efficiency of PI without generating unwanted iodine byproducts, showcasing its potential for environmentally friendly removal of organic pollutants.

Article Abstract

In this study, Ru(III) ions were utilized to activate periodate (PI) for oxidation of trace organic pollutants (TOPs, e.g., carbamazepine (CBZ)). The Ru(III)/PI system can significantly promote the oxidation of CBZ in a wide initial pH range (3.0-11.0) at 1 μM Ru(III), showing much higher performance than transition metal ions (i.e., Fe(II), Co(II), Zn(II), Fe(III), Cu(II), Ni(II), Mn(II), and Ce(III)) and noble metal ion (i.e., Ag(I), Pd(II), Pt(II), and Ir(III)) activated PI systems. Probe experiments, UV-vis spectra, and X-ray absorption near-edge structure (XANES) spectra confirmed high-valent Ru-oxo species (Ru(V)=O) as the dominant oxidant in the process. Because of the dominant role of Ru(V)=O, the Ru(III)/PI process exhibited a remarkable selectivity and strong anti-interference in the oxidation of TOPs in complex water matrices. The Ru(V)=O species can undertake 1-e and 2-e transfer reactions via the catalytic cycles of Ru(V)=O → Ru(IV) → Ru(III) and Ru(V)=O → Ru(III), respectively. The utilization efficiency of PI in the Ru(III)/PI process for the oxidation of TOPs can approach 100% under optimal conditions. PI stoichiometrically transformed into IO without production of undesired iodine species (e.g., HOI and I). This study developed an efficient and environmentally benign advanced oxidation process for rapid removal of TOPs and enriched understandings on reactivity of Ru(V)=O and Ru catalytic cycles.

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Source
http://dx.doi.org/10.1021/acs.est.3c02582DOI Listing

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