Molecular Oxygen Activation by Citric Acid Boosted Pyrite–Photo–Fenton Process for Degradation of PPCPs in Water

Abstract

Pyrite has been used in photo-Fenton reactions for the degradation of pollutants, but the application of photo-Fenton processes with extra H₂O₂ in real water/wastewater treatment has still been limited by the economic cost of H₂O₂ and artificial light sources. Herein, citric acid (CA) and simulated/natural sunlight are used to develop a pyrite-based photo-Fenton system (pyrite-CA-light) in situ generating H₂O₂ through the enhanced activation of molecular oxygen. The degradation of pharmaceuticals and personal care products (PPCPs), especially acetaminophen (APAP) as the main target pollutant, in the pyrite-CA-light system was investigated. The effects of influencing factors such as various organic acids, APAP concentration, pH, pyrite dosage, CA concentration and co-existing anions (HCO₃^-, Cl^-, NO₃^-, SO₄^2- and H₂PO₄^-) were examined. At a pyrite dosage of 0.1 g L^-1, CA concentration of 0.6 mM and an initial pH of 6.0, the degradation efficiency of APAP (30 μM) was 99.1% within 30 min under the irradiation of xenon lamp (70 W, λ ≥ 350 nm). Almost the same high efficiency of APAP degradation (93.9%) in the system was achieved under natural sunlight irradiation (ca. 650 W m^-2). The scavenging experiments revealed that the dominant active species for degrading APAP was hydroxyl radical (HO^•). Moreover, a quantitative structural-activity relationship (QSAR) model for pseudo-first-order rate constants (<i>k</i>_obs) was established with a high significance (R² = 0.932, <i>p</i> = 0.001) by using three descriptors: octanol-water partition coefficient (log<i>K</i>ow), dissociation constant (pK_a) and highest occupied molecular orbital (HOMO). This work provides an innovative strategy of the photo-Fenton process for the degradation of PPCPs using natural minerals and ordinary carboxylic acid under sunlight.