4.7 Article

Efficient removal of trifluoroacetic acid from water using surface-modified activated carbon and electro-assisted desorption

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JOURNAL OF HAZARDOUS MATERIALS
卷 436, 期 -, 页码 -

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DOI: 10.1016/j.jhazmat.2022.129051

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Trifluoroacetic acid; Electrosorption; Activated carbon; Surface modification

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The research shows that surface defunctionalized activated carbon felt (DeACF) can effectively adsorb trifluoroacetic acid (TFA) through enhanced interactions between hydrophobic carbon surface and CF3 moieties. The electro-assisted TFA desorption using Na2SO4 as electrolyte shows high efficiency in recovering TFA. Despite the decrease in adsorption capacity caused by surface oxidation, the system stability can still be maintained.
Trifluoroacetic acid (TFA) is a very persistent, very mobile substance (vPvM) with potential toxicity, and causes increasing environmental concerns worldwide. Conventional wastewater treatment strategies are inefficient for selective TFA removal in the presence of inorganic anions. Here we show that surface defunctionalized activated carbon felt (DeACF) carrying anion exchange sites exhibits an outstanding adsorption efficiency towards TFA thanks to introduced electrostatic attraction and enhanced interactions between hydrophobic carbon surface and CF3 moieties (qmax = 30 mg/g, Kd = (840 +/- 80) L/kg at cTFA = 3.4 mg/L in tap water). Flow-cell experiments demonstrated a strongly favored TFA uptake by DeACF from tap water over Cl- and SO42- but a remarkable coadsorption of the inorganic water contaminant NO3- . Electro-assisted TFA desorption using 10 mM Na2SO4 as electrolyte and oxidized ACF as anode showed high recoveries of >= 87% at low cell voltages (< 1.1 V). Despite an initial decrease in TFA adsorption capacity (by 33%) caused by partial surface oxidation of DeACF after the 1st ad-/desorption cycle, the system stability was fully maintained over the next 4 cycles. Such electro-assisted 'trap&release' approach for TFA removal can be exploited for on-site regenerable adsorption units and as a pre-concentration step combined with degradation technologies.

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