4.7 Article

UV 222 nm Emission from KrCl* Excimer Lamps Greatly Improves Advanced Oxidation Performance in Water Treatment

期刊

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.estlett.2c00472

关键词

LPUV; KrCl* excimer; hydroxyl radical; hydrogen peroxide; nitrate; advanced oxidation processes (AOPs)

资金

  1. National Science Foundation-BiNational Science Foundation (NSF-BSF) Award [CBET-1931168]

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KrCl* excimer lamps emitting at 222 nm have the potential to enhance ultraviolet (UV)-based advanced oxidation efficiency. Experiments comparing low-pressure UV (LPUV) and KrCl* excimer lamps were conducted in ultrapure water and groundwater, with different radical promoters. The results showed that the concentration of hydroxyl radicals (.OH) achieved using KrCl*/NO3- UV/AOP was significantly higher than that of conventional LPUV/H2O2, both in ultrapure water and groundwater. Several research gaps were identified to facilitate the adoption of KrCl* for UV/AOP in the future.
KrCl* excimer lamps emitting at 222 nm hold potential for enhancing ultraviolet (UV)-based advanced oxidation efficiency. Experiments were conducted in both ultrapure water and groundwater comparing low-pressure UV (LPUV) and KrCl* excimer lamps, with two different radical promoters [hydrogen peroxide (H2O2) and nitrate (NO3-)]. Compared to that of conventional LPUV/H2O2, the steady-state hydroxyl radical (.OH) concentration achieved in the KrCl*/NO3- UV/AOP was 13.1 times greater while that for the KrCl*/H2O2 process was 9.4 times greater in ultrapure water; the values in groundwater were 7.3 and 3.7 times greater, respectively, all using a standard single probe compound decay method as a proxy for .OH radical generation. This work identified several research gaps that must be addressed to facilitate adoption of KrCl* for UV/AOP, including development of methods for comparing UV/AOPs that utilize different UV radiation sources and radical promoters, a need to acquire more information about direct photolysis quantum yields at 222 nm for contaminants of concern, and the impact of the background water matrix constituents on radical promotion or formation of any byproducts, especially in the presence of NO3- as a radical promoter.

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