Destruction of Per- and Polyfluoroalkyl Substances (PFAS) with Advanced Reduction Processes (ARPs): A Critical Review
Junkui Cui1, Panpan Gao1,2, Yang Deng1
1Department of Earth and Environmental Studies, Montclair State University, Montclair, New Jersey 07043, United States.
Advanced reduction processes effectively destroy persistent per- and polyfluoroalkyl substances (PFAS) in water using hydrated electrons (eaq-). This review details PFAS destruction mechanisms and factors influencing efficiency for practical water treatment applications.
Area of Science:
- Environmental Chemistry
- Water Treatment Technologies
- Advanced Oxidation Processes
Background:
- Per- and polyfluoroalkyl substances (PFAS) are persistent environmental contaminants.
- Conventional water treatment methods are often ineffective for PFAS removal.
- Advanced reduction processes (ARPs) offer a promising alternative for PFAS destruction.
Purpose of the Study:
- To critically review the mechanisms and performance of reductive destruction of PFAS using hydrated electrons (eaq-).
- To overview the generation of eaq- in ARP systems like UV/sulfite and UV/iodide.
- To identify research needs for practical PFAS control in water industries.
Main Methods:
- Literature review of advanced reduction processes for PFAS destruction.
- Analysis of PFAS degradation mechanisms based on chemical structure and head groups.
- Evaluation of factors influencing PFAS degradation and defluorination efficiencies.
Main Results:
- Degradation pathways of various PFAS (PFOA, PFOS, PFCAs, PFSAs) are heavily influenced by their head groups and, for some, fluoroalkyl chain length.
- Hydrated electrons (eaq-) generated in ARPs are key to PFAS destruction.
- Solution chemistry (pH, dissolved oxygen, humic acid, nitrate) and operating factors (solute dose, temperature) significantly impact PFAS degradation and defluorination.
Conclusions:
- ARPs, particularly UV/sulfite and UV/iodide systems, show significant potential for PFAS destruction via eaq-.
- Understanding degradation mechanisms and influencing factors is crucial for optimizing PFAS removal.
- Further research is needed to translate these findings into effective industrial water treatment strategies.
Related Concept Videos
Protecting Groups for Aldehydes and Ketones: Introduction
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
Radical Formation: Elimination
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Phase I Reactions: Reductive Reactions


