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Updated: Jan 20, 2026

In Situ Monitoring of the Accelerated Performance Degradation of Solar Cells and Modules: A Case Study for CuIn,GaSe2 Solar Cells
Published on: October 3, 2018
Photo-Fenton-like degradation of bisphenol A by persulfate and solar irradiation
Marina Khandarkhaeva1, Agniya Batoeva2, Marina Sizykh2
1Baikal Institute of Nature Management of Siberian Branch of the Russian Academy of Sciences, 6, Sakhyanova St., Ulan-Ude, 670047, Russia; Okinawa Institute of Science and Technology, 1919-1 Tancha, Onna-son, Okinawa-ken, 904-0495, Japan.
Abstract:
This work evaluates the feasibility of a solar-enhanced Fenton-like process using S2O82- (PS) and Fe2+ for the elimination of BPA, a model endocrine-disruption compound. This comparative study of BPA removal showed that among the approaches employed, the effectiveness of BPA degradation (10 mg/L) decreased in the order: Solar/PS/Fe2+> Solar/PS > PS/Fe2+> Solar/Fe2+> Solar. The complete degradation of BPA was achieved by Solar/PS/Fe2+ treatment at a [PS]:[BPA] ratio of 20 in less than t30W 5 in deionised water. The high efficiency of the Solar/PS/Fe2+ process revealed a synergistic effect (ϕ = 2.38) between the applied activation agents on the formation of reactive oxygen species (ROS) and subsequent decomposition of BPA. The treatment was accompanied by total organic carbon (TOC) removal (44%) in 45 min. Sequential generation of reactive oxygen species has made Solar/PS/Fe2+ a kinetically effective process for removing BPA without accumulation of toxic intermediates. The reaction rate followed pseudo-first-order kinetics that increased with increasing PS and Fe2+ concentrations. Experimental evidence suggests that exposure to solar irradiation maintains suitable quantities of free Fe2+ in the reaction mixture, even at low catalyst concentrations (the molar ratio of [PS]:[Fe2+] varied from 1:0.01 to 1:0.08). The effects of HCO3-, SO42-, and Cl- were also examined. As expected, HCO3- and SO42- inhibited BPA oxidation. The effect of Cl- on the oxidation efficiency of BPA in Fenton-like systems depends not only on actual Cl- concentrations but it is also highly influenced by molar ratios of Cl- to oxidant and catalyst. Inhibition, which was caused by Cl- in the mM range can be overcome by prolonging the reaction time or increasing the initial Fe2+concentration. Finally, the efficiency of Solar/PS/Fe2+ process was examined in diluted natural surface water and wastewater effluent. On eliminating the buffering action of HCO3-/CO32- ions by lowering the pH value to 4.5, complete BPA degradation was achieved in all real water matrices.
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