The present paper investigates the adsorption performance of pinewood-derived biochars produced at two pyrolysis temperatures (850 degrees C, PW-A; 1000 degrees C, PW-B), including sieved fractions (PW-A1 and PW-A2) and a functionalized variant (PW-C), for the removal of five short- and intermediate-chain PFASs (PFBA, PFBS, PFHxA, PFHxS, and GenX) from water under continuous-flow conditions. Adsorption behavior was evaluated using Freundlich and Hill isotherm models. The Hill model provided a superior fit for most PFAS-adsorbent systems, highlighting the importance of cooperativity effects, particularly for short-chain PFASs. In single-compound experiments, PFBS and GenX showed the highest adsorption capacities (up to 82.3 and 68.5 mg g(-1)), while PFBA and PFHxA exhibited the lowest. Among the tested materials, biochar produced at 1000 degrees C (PW-B) consistently demonstrated the highest adsorption efficiency. Compared to activated carbon, PW-B showed comparable performance for PFBA, PFBS, PFHxA and PFHxS and significantly better performance for GenX. In mixed-PFAS systems, competitive effects reduced adsorption capacity and cooperativity. Sulfonic PFASs showed higher affinity than carboxylic PFASs, following the trend PFHxS > PFBS > PFHxA > PFBA. Overall, the results demonstrate that waste-derived biochar represents a low-cost and sustainable alternative for PFAS removal in realistic water-treatment scenarios, supporting scalable solutions aligned with global environmental goals.

Pinewood Biochar as an Affordable Adsorbent for Short- and Medium-Chain PFAS Removal from Contaminated Water / Simonetti, G.; Di Filippo, P.; Pomata, D.; Riccardi, C.; Buiarelli, F.; Parisi, S.; Petrangeli Papini, M.; Senofonte, M.; Lorini, L.. - In: MOLECULES. - ISSN 1420-3049. - 31:7(2026). [10.3390/molecules31071100]

Pinewood Biochar as an Affordable Adsorbent for Short- and Medium-Chain PFAS Removal from Contaminated Water

Simonetti G.
;
Di Filippo P.;Pomata D.;Buiarelli F.;Petrangeli Papini M.;Senofonte M.
;
Lorini L.
2026

Abstract

The present paper investigates the adsorption performance of pinewood-derived biochars produced at two pyrolysis temperatures (850 degrees C, PW-A; 1000 degrees C, PW-B), including sieved fractions (PW-A1 and PW-A2) and a functionalized variant (PW-C), for the removal of five short- and intermediate-chain PFASs (PFBA, PFBS, PFHxA, PFHxS, and GenX) from water under continuous-flow conditions. Adsorption behavior was evaluated using Freundlich and Hill isotherm models. The Hill model provided a superior fit for most PFAS-adsorbent systems, highlighting the importance of cooperativity effects, particularly for short-chain PFASs. In single-compound experiments, PFBS and GenX showed the highest adsorption capacities (up to 82.3 and 68.5 mg g(-1)), while PFBA and PFHxA exhibited the lowest. Among the tested materials, biochar produced at 1000 degrees C (PW-B) consistently demonstrated the highest adsorption efficiency. Compared to activated carbon, PW-B showed comparable performance for PFBA, PFBS, PFHxA and PFHxS and significantly better performance for GenX. In mixed-PFAS systems, competitive effects reduced adsorption capacity and cooperativity. Sulfonic PFASs showed higher affinity than carboxylic PFASs, following the trend PFHxS > PFBS > PFHxA > PFBA. Overall, the results demonstrate that waste-derived biochar represents a low-cost and sustainable alternative for PFAS removal in realistic water-treatment scenarios, supporting scalable solutions aligned with global environmental goals.
2026
PFAS removal; biochar; continuous-flow adsorption; pinewood-derived biochar; short-chain PFAS; sustainable adsorbents
01 Pubblicazione su rivista::01a Articolo in rivista
Pinewood Biochar as an Affordable Adsorbent for Short- and Medium-Chain PFAS Removal from Contaminated Water / Simonetti, G.; Di Filippo, P.; Pomata, D.; Riccardi, C.; Buiarelli, F.; Parisi, S.; Petrangeli Papini, M.; Senofonte, M.; Lorini, L.. - In: MOLECULES. - ISSN 1420-3049. - 31:7(2026). [10.3390/molecules31071100]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1767352
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