Advanced reduction processes (ARPs) have emerged as a promising method for destruction of persistent per- and polyfluoroalkyl substances (PFAS) in water due to the generation of short-lived and highly reductive hydrated electrons (eaq-). This study provides a critical review on the mechanisms and performance of reductive destruction of PFAS with eaq-. Unique properties of eaq- and its generation in different ARP systems, particularly UV/sulfite and UV/iodide, are overviewed. Different degradation mechanisms of PFAS chemicals, such as perfluorooctanoic acid (PFOA), perfluorooctanesulfonate (PFOS), and others (e.g., short chain perfluorocarboxylic acids (PFCAs) and perfluorosulfonic acids (PFSAs), per- and polyfluoro dicarboxylic acids, and fluorotelomer carboxylic acids), are reviewed, discussed, and compared. The degradation pathways of these PFAS chemicals rely heavily upon their head groups. For specific PFAS types, fluoroalkyl chain lengths may also affect their reductive degradation patterns. Degradation and defluorination efficiencies of PFAS are considerably influenced by solution chemistry parameters and operating factors, such as pH, dose of chemical solute (i.e., sulfite or iodide) for eaq- photoproduction, dissolved oxygen, humic acid, nitrate, and temperature. Furthermore, implications of the state-of-the-art knowledge on practical PFAS control actions in water industries are discussed and the priority research needs are identified.

Destruction of Per- and Polyfluoroalkyl Substances (PFAS) with Advanced Reduction Processes (ARPs): A Critical Review.

Impact of humic acid on the photoreductive degradation of perfluorooctane sulfonate (PFOS) by UV/Iodide process.

Nitroaromatic compounds (NACs) are extensively used in different industries and are synthesized in large quantity due to their heavy demand worldwide. The broad use of NACs poses a serious pollution threat. The treatment processes used for the removal of NACs are not effective and sustainable, leading to their release into the environment. The nitro group attached to benzene ring makes the compounds recalcitrant due to which they persist in the environment. Being hazardous to human as well as other living organisms, NACs are listed in the USEPA's priority pollutant group. This review provides updated information on the sources of NACs, prevalence in different environmental matrices, and recent developments in methods of their detection, with emphasis on current trends as well as future prospects. The harmful effects of NACs due to exposure through different routes are also highlighted. Further, the technologies reported for the treatment of NACs, including physico-chemical and biological methods, and the challenges faced for their effective implementation are discussed. Thus, the review discusses relevant issues in detail making suitable recommendations, which can be helpful in guiding further research in this subject.

Environmental persistence, hazard, and mitigation challenges of nitroaromatic compounds

Ultraviolet photochemical reaction of sulfite (SO32–) photosensitizer generates strongly reducing hydrated electrons (eaq–; NHE = −2.9 V) that have been shown to effectively degrade individual per-...

Destruction of Per- and Polyfluoroalkyl Substances (PFASs) in Aqueous Film-Forming Foam (AFFF) with UV-Sulfite Photoreductive Treatment.

Here we describe a unique process that achieves complete defluorination and decomposition of perfluorinated compounds (PFCs) which comprise one of the most recalcitrant and widely distributed classes of toxic pollutant chemicals found in natural environments. Photogenerated hydrated electrons derived from 3-indole-acetic-acid within an organomodified clay induce the reductive defluorination of co-sorbed PFCs. The process proceeds to completion within a few hours under mild reaction conditions. The organomontmorillonite clay promotes the formation of highly reactive hydrated electrons by stabilizing indole radical cations formed upon photolysis, and prevents their deactivation by reaction with protons or oxygen. In the constrained interlayer regions of the clay, hydrated electrons and co-sorbed PFCs are brought in close proximity thereby increasing the probability of reaction. This novel green chemistry provides the basis for in situ and ex situ technologies to treat one of the most troublesome, recalcitrant and ubiquitous classes of environmental contaminants, i.e., PFCs, utilizing innocuous reagents, naturally occurring materials and mild reaction conditions.

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Complete Defluorination of Perfluorinated Compounds by Hydrated Electrons Generated from 3-Indole-acetic-acid in Organomodified Montmorillonite.

A new photoreduction pathway for nitro-aromatic compounds (NACs) and the underlying degradation mechanism are described. 1,3-Dinitrobenzene was reduced to 3-nitroaniline by the widely distributed aromatic molecule indole; the reaction is facilitated by montmorillonite clay mineral under both simulated and natural sunlight irradiation. The novel chemical reaction is strongly affected by the type of exchangeable cation present on montmorillonite. The photoreduction reaction is initiated by the adsorption of 1,3-dinitrobenzene and indole in clay interlayers. Under light irradiation, the excited indole molecule generates a hydrated electron and the indole radical cation. The structural negative charge of montmorillonite plausibly stabilizes the radical cation hence preventing charge recombination. This promotes the release of reactive hydrated electrons for further reductive reactions. Similar results were observed for the photoreduction of nitrobenzene. In situ irradiation time-resolved electron paramagnetic...

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Yong Guo

Papers

Enhanced Photoreduction of Nitro-aromatic Compounds by Hydrated Electrons Derived from Indole on Natural Montmorillonite.