4.7 Article

Degrading arsanilic acid and adsorbing the released inorganic arsenic simultaneously in aqueous media with CuFe2O4 activating peroxymonosulfate system: Factors, performance, and mechanism

期刊

CHEMICAL ENGINEERING JOURNAL
卷 424, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.128537

关键词

Arsanilic acid; Peroxymonosulfate; Toxicity assessment; Inorganic arsenic; Adsorption

资金

  1. National Natural Science Foundation of China [51579097, 51521006, 51879102]
  2. Science & Technology Plan Project of Hunan Province [2018SK2047]

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In this study, a one-step process using CuFe2O4 activated peroxymonosulfate was employed to investigate the degradation of arsanilic acid and the absorption of released inorganic arsenic. Results showed that over 99% of ASA could be converted to As(V) and adsorbed on CuFe2O4 under specific conditions. Various factors had different effects on the degradation of ASA.
Arsanilic acid (ASA) is widely used as a feed additive in poultry production that tends to convert to highly toxic inorganic arsenic species in the natural environment. Herein, one-step process by CuFe2O4 activating peroxymonosulfate (PMS) was employed for ASA degradation and released inorganic arsenic absorption from aqueous media. The effect of some key parameters including catalyst dosage (0-0.5 g/L), PMS concentration (0-500 mu M), initial pH (3.4-10.5) and water matrices (Cl, HCO3, NO3-, Fe2+, Fe3+, Mg2+, Ca2+, NH4+ and humic acid) on ASA degradation were investigated. More than 99% of ASA (26.72 mu M, 2 mg-As/L) was converted to As(V), and 84.65% of it was adsorbed on CuFe2O4 simultaneously within 90 min at 0.3 g/L CuFe2O4, 200 mu M PMS at initial pH 7. Specifically, the presence of humic acid significantly inhibited ASA degradation. Cl had a dual effect, HCO3- and Fe2+ had a promoting effect and some common cations (Fe3+, Mg2+, Ca2+, and NH4+) had negligible effect on ASA conversion. FTIR and XPS analyses indicated the removal of inorganic arsenic followed the mechanism of inner-sphere complex. Radicals analyses showed that O-2(center dot-), center dot OH and SO4 center dot- (free and surface-bound) accounted for arsenic species oxidation in the CuFe2O4/PMS system. Besides, ASA could also be oxidized to the nitrated product (nitarsone) through a non-radical pathway by PMS alone. The degradation products of ASA were identified by LC/MS/MS and the degradation pathways were proposed, and their toxicity was assessed using luminescent bacteria Vibrio fischeri. Moreover, the recovered catalyst exhibited high stability and reusability tested by SEM, TEM, XRD and leaching ions experiments.

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