Valorization of steel slag towards a Fenton-like catalyst for the degradation of paraben by activated persulfate

被引:45
|
作者
Matthaiou, Vasiliki [1 ]
Oulego, Paula [2 ]
Frontistis, Zacharias [1 ,3 ]
Collado, Sergio [2 ]
Hela, Dimitra [4 ]
Konstantinou, Ioannis K. [4 ]
Diaz, Mario [2 ]
Mantzavinos, Dionissios [1 ,3 ]
机构
[1] Univ Patras, Dept Chem Engn, Caratheodory 1, GR-26504 Patras, Greece
[2] Univ Oviedo, Dept Chem & Environm Engn, C Julian Claveria 8, E-33006 Oviedo, Asturias, Spain
[3] INVALOR Res Infrastruct Waste Valorizat & Sustain, Caratheodory 1,Univ Campus, GR-26504 Patras, Greece
[4] Univ Ioannina, Dept Chem, GR-45110 Ioannina, Greece
关键词
Advanced oxidation processes; Micro-pollutant; Slag; Steel; Water; Valorization; OXYGEN FURNACE SLAG; WASTE-WATER TREATMENT; HYDROGEN-PEROXIDE; AQUEOUS-SOLUTION; RATE CONSTANTS; PHANEROCHAETE-CHRYSOSPORIUM; PARTICLE ELECTRODES; RADICAL REACTIONS; IRON(III) OXIDES; METHYLENE-BLUE;
D O I
10.1016/j.cej.2018.11.198
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Different iron-containing materials (named as S1-S5) obtained through an oxidative digestion in acid media of basic oxygen furnace (BOF) slag were studied for the activation of sodium persulfate (SPS) to generate active radicals for the oxidation of propylparaben (PP), a model endocrine disruptor, in water. It was found that the materials with magnetite in its composition (S1, S2 and S3) effectively catalyze SPS for the removal of PP, and the reaction followed a pseudo-first-order kinetic pattern (r(2) > 0.96). Within 90 min, a removal of approximately 90% of 0.4 mg/L of PP was accomplished by 1 g/L of SPS in presence of 50 mg/L of S1 catalyst with negligible iron leaching. Besides, the oxidation of PP was favored by higher dosages of S1 catalyst and SPS oxidant, lower initial PP concentration and neutral or alkaline pH. The generation of sulfate and hydroxyl radical was indirectly validated from the scavenging tests, using tert-butanol and methanol as scavenging agents. Based on the XPS analysis, it can be pointed out that the radical generation was due to the presence of Fe2+-Fe3+ on the surface of the catalysts. A degradation pathway based on the transformation products (TPs) resulting from PP degradation was also proposed.
引用
收藏
页码:728 / 739
页数:12
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