A FAIR comparison of activated carbon, biochar, cyclodextrins, polymers, resins, and metal organic frameworks for the adsorption of per- and polyfluorinated substances

• Adsorption of 44 PFAS was evaluated across four different adsorbent groups. • Activated carbon and biochar had the highest K d for PFAS with ≥ 7C-F bonds. • Cyclodextrins and resins outperformed activated carbons and biochars for PFAS≤4C-F bonds. • Structural PFAS properties could be related to adsorption behavior. • Random Forest Regressor model can predict adsorption to AC and BC, not for others. Per- and polyfluorinated substances (PFAS) have complex sorption behaviors, complicating removal from water and selection of suitable adsorbents. We evaluated adsorption of 44 PFAS across four adsorbent groups: activated carbon and biochar (AC and BC), cyclodextrin-based adsorbents (cyclodextrins), polymer-based adsorbents and resins, and inorganic adsorbents and metal organic frameworks (MOFs). We analyzed over 500 adsorption coefficients (K d ) from literature, calculated at aqueous equilibrium concentration of 1 ± 0.3 µg/L under comparable experimental conditions. On average, K d of AC and BC exceeded 10 7 L/kg for PFAS with C-F bonds > 7, unlike other adsorbents with K d < 10 7 . This trend holds for C-F bonds ≥ 4. Cyclodextrins, polymer-based adsorbents and resins outperform AC and BC for C-F bonds < 4. For AC and BC, K d follows the order PFOS>PFOA>PFBS>PFBA, with adsorption increasing with increasing point of zero charge of the adsorbent. For AC and BC, as well as cyclodextrins, K d values were related to PFAS hydrophobicity and steric properties. Additionally, adsorption was influenced by head group type, non-fluorinated carbon atoms, and the presence of oxygen and/or chlorine in the PFAS. No clear relationship was found for the other adsorbents. Adsorption prediction using a Random Forest Regressor and literature data was feasible for AC and BC, but not for other adsorbents. Cyclodextrins outperform AC and BC for removing PFAS across varying mobilities from water, whereas AC and BC are superior for low mobility PFAS. To support further data use all data and code used are freely available, following FAIR data principles.

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Institutions

Publication Details

Journal
Chemical Engineering Journal
Published
2024-09-03
DOI
https://doi.org/10.1016/j.cej.2024.155456
Citations
23
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
5.76
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article

A FAIR comparison of activated carbon, biochar, cyclodextrins, polymers, resins, and metal organic frameworks for the adsorption of per- and polyfluorinated substances

Gabriel Sigmund, Adelene Lai, Falk Harnisch, Navid Saeidi
23 citations
Chemical Engineering Journal
Per- and polyfluoroalkyl substances research
5.76
article

A FAIR comparison of activated carbon, biochar, cyclodextrins, polymers, resins, and metal organic frameworks for the adsorption of per- and polyfluorinated substances

Gabriel Sigmund, Adelene Lai, Falk Harnisch, Navid Saeidi
article en
23 citations

Abstract

• Adsorption of 44 PFAS was evaluated across four different adsorbent groups. • Activated carbon and biochar had the highest K d for PFAS with ≥ 7C-F bonds. • Cyclodextrins and resins outperformed activated carbons and biochars for PFAS≤4C-F bonds. • Structural PFAS properties could be related to adsorption behavior. • Random Forest Regressor model can predict adsorption to AC and BC, not for others. Per- and polyfluorinated substances (PFAS) have complex sorption behaviors, complicating removal from water and selection of suitable adsorbents. We evaluated adsorption of 44 PFAS across four adsorbent groups: activated carbon and biochar (AC and BC), cyclodextrin-based adsorbents (cyclodextrins), polymer-based adsorbents and resins, and inorganic adsorbents and metal organic frameworks (MOFs). We analyzed over 500 adsorption coefficients (K d ) from literature, calculated at aqueous equilibrium concentration of 1 ± 0.3 µg/L under comparable experimental conditions. On average, K d of AC and BC exceeded 10 7 L/kg for PFAS with C-F bonds > 7, unlike other adsorbents with K d < 10 7 . This trend holds for C-F bonds ≥ 4. Cyclodextrins, polymer-based adsorbents and resins outperform AC and BC for C-F bonds < 4. For AC and BC, K d follows the order PFOS>PFOA>PFBS>PFBA, with adsorption increasing with increasing point of zero charge of the adsorbent. For AC and BC, as well as cyclodextrins, K d values were related to PFAS hydrophobicity and steric properties. Additionally, adsorption was influenced by head group type, non-fluorinated carbon atoms, and the presence of oxygen and/or chlorine in the PFAS. No clear relationship was found for the other adsorbents. Adsorption prediction using a Random Forest Regressor and literature data was feasible for AC and BC, but not for other adsorbents. Cyclodextrins outperform AC and BC for removing PFAS across varying mobilities from water, whereas AC and BC are superior for low mobility PFAS. To support further data use all data and code used are freely available, following FAIR data principles.

Chemical Engineering JournalVol. 498
Helmholtz Centre for Environmental Research (DE), Wageningen University & Research (NL)
Openalex Percentile: Top 3%
Per- and polyfluoroalkyl substances research
5.76
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