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Sonolysis of per- and poly fluoroalkyl substances (PFAS): A meta-analysis

Journal

ULTRASONICS SONOCHEMISTRY
Volume 87, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ultsonch.2022.105944

Keywords

PFAS; Sonolysis; Literature review; Meta-analysis; Parametric; Ultrasonic degradation

Funding

  1. Arcadis Consulting (UK) , Ltd.
  2. University of Surrey
  3. Royal Society Research Grant
  4. Royal Academy of Engineering Industrial Fellowships Scheme [IFS1819\34]
  5. Arcadis, United Kingdom, Royal Society Research Grant [86200452]

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This paper summarizes the latest progress in PFAS sonolysis technology, including reaction mechanisms, kinetics, intermediates, products, and measurement techniques. The study found that the mechanisms of mid-high frequency sonolysis are similar, while the mechanisms of low frequency sonolysis are related to oxidative species. Stoichiometric reaction equations were derived for PFOA and PFOS sonolysis, and fluorinated intermediate products were derived for different PFAS. The study also revealed the concentration range for the transition of PFOA/S kinetics and derived optimum values for ultrasonic frequency, concentration, temperature, and pH range.
Human ingestion of per-and polyfluoroalkyl substances (PFAS) from contaminated food and water is linked to the development of several cancers, birth defects and other illnesses. The complete mineralisation of aqueous PFAS by ultrasound (sonolysis) into harmless inorganics has been demonstrated in many studies. However, the range and interconnected nature of reaction parameters (frequency, power, temperature etc.), and variety of reaction metrics used, limits understanding of degradation mechanisms and parametric trends. This work summarises the state-of-the-art for PFAS sonolysis, considering reaction mechanisms, kinetics, intermediates, products, rate limiting steps, reactant and product measurement techniques, and effects of co-contaminants. The meta-analysis showed that mid-high frequency (100 - 1,000 kHz) sonolysis mechanisms are similar, regardless of reaction conditions, while the low frequency (20 - 100 kHz) mechanisms are specific to oxidative species added, less well understood, and generally slower than mid-high frequency mechanisms. Arguments suggest that PFAS degradation occurs via adsorption (not absorption) at the bubble interface, followed by headgroup cleavage. Further mechanistic steps toward mineralisation remain to be proven. For the first time, complete stoichiometric reaction equations are derived for perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) sonolysis, which add H2 as a reaction product and consider CO an intermediate. Fluorinated intermediate products are derived for common, and more novel PFAS, and a naming system proposed for novel perfluoroether carboxylates. The meta-analysis also revealed the transition between pseudo first and zero order PFOA/S kinetics commonly occurs at 15 - 40 mu M. Optimum values of; ultrasonic frequency (300 - 500 kHz), concentration (> 15 - 40 mu M), temperature (asymptotic to 120 C), and pH range (3.2 - 4) for rapid PFOX degradation are derived by evaluation of prior works, while optimum values for the dilution factor applied to PFAS containing firefighting foams and applied power require further work. Rate limiting steps are debated and F- is shown to be rate enhancing, while SO(4)(2-)and CO2 by products are theorised to be rate limiting. Sonolysis was compared to other PFAS destructive technologies and shown to be the only treatment which fully mineralises PFAS, degrades different PFAS in order of decreasing hydrophobicity, is parametrically well studied, and has low-moderate energy requirements (several kWh g(-1) PFAS). It is concluded that sonolysis of PFAS in environmental samples would be well incorporated within a treatment train for improved efficiency.

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