CuFeS2 supported on dendritic mesoporous silica-titania for persulfate-assisted degradation of sulfamethoxazole under visible light

被引:15
作者
Ntelane, Tau S. [1 ,2 ]
Feleni, Usisipho [1 ]
Mthombeni, Nomcebo H. [2 ,3 ]
Kuvarega, Alex T. [1 ]
机构
[1] Univ South Africa, Coll Sci Engn & Technol, Inst Nanotechnol & Water Sustainabil, ZA-1709 Johannesburg, South Africa
[2] Univ South Afr, Coll Sci Engn & Technol, Dept Chem Engn, ZA-1710 Johannesburg, South Africa
[3] Durban Univ Technol, Fac Engn & Built Environm, Dept Chem Engn, POB 1334, ZA-4000 Durban, South Africa
关键词
Sulfamethoxazole; TiO2; Chalcopyrite; Sulfate radicals. Advanced oxidation processes; CHALCOPYRITE CUFES2; PHOTOCATALYTIC PERFORMANCE; HYDROTHERMAL SYNTHESIS; EFFICIENT DEGRADATION; FIBROUS NANOSILICA; ACTIVATION; NANOCOMPOSITE; CATALYSIS; NANOPARTICLES; OXIDATION;
D O I
10.1016/j.jcis.2023.10.077
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Sulfamethoxazole (SMX) is a prevalent sulfonamide antibiotic found in the environment, and it has a variety of detrimental effects on environmental sustainability and water safety. Recently, the combination of photocatalysis and sulfate radical-based advanced oxidation processes (SR-AOPs) has attracted a lot of interest as a viable technique for degradation of refractory pollutants. In this study, a visible light active CuFeS2 supported on dendritic mesoporous silica-titania (CuFeS2-DMST) photocatalyst was synthesized to improve the ability of TiO2 to activate persulfate (PS) by introducing CuFeS2 (Fe2+/Fe3+, Cu+/Cu2+ redox cycles). The CuFeS2-DMST/PS/Vis system demonstrated superior SMX degradation efficiency (88.9%, 0.0146 min(-1)) than TiO2 because of reduced e(-)/h(+) recombination, excellent charge separation and mobility, and a greater surface area than TiO2. Furthermore, after four consecutive photocatalytic cycles, the system demonstrated moderate stability. From chemical quenching tests, O-2(center dot)-, h(+), O-1(2), SO4 center dot- and (OH)-O-center dot were found to be the main reactive oxidizing species. The formed intermediates during the degradation process were identified, and degradation mechanisms were proposed. This study proposes a viable technique for activating PS using a low-cost, stable, and high-surface-area TiO2-based photocatalyst, and this concept can be applied to design photocatalysts for water treatment.
引用
收藏
页码:660 / 676
页数:17
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