Exploring raw scoria as an iron catalyst for Fenton-based degradation of pharmaceutical pollutants: kinetic and mechanistic insights

IF 2.1 4区 化学 Q4 CHEMISTRY, PHYSICAL
Amel Hamadi, Fayçal Finnouche, Hiba Kais, Zohra Bensaadi-Ouznadji, Nacera Yeddou-Mezenner
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引用次数: 0

Abstract

This study investigates the removal of hydroxychloroquine (HCQ) from aqueous solutions using scoria as a natural iron source in the Fenton process. The scoria was characterized by X-ray fluorescence (XRF) and X-ray diffraction (XRD) to determine its elemental composition and crystalline structure. The effects of key operational parameters, including initial pH, hydrogen peroxide concentration, scoria dosage (0.1–1 g L⁻1), HCQ concentration (5–25 mg L⁻1), and reaction temperature, were systematically evaluated. Under optimal conditions (HCQ = 10 mg L⁻1, [H2O2] = 13 mM, scoria dosage = 0.5 g L⁻1, and temperature = 24 °C), a maximum removal efficiency of 98% was achieved. Kinetic analysis indicated that the degradation followed a pseudo-second-order model. These findings demonstrate that scoria is an effective and low-cost catalyst for Fenton-based degradation of pharmaceutical contaminants in water.

探索原矿渣作为铁催化剂的fenton降解药物污染物:动力学和机理的见解
本研究研究了在Fenton工艺中利用矿渣作为天然铁源去除水溶液中的羟氯喹(HCQ)。采用x射线荧光(XRF)和x射线衍射(XRD)对其进行了表征,确定了其元素组成和晶体结构。系统地评估了初始pH、双氧水浓度、炉渣用量(0.1-1 g L - 1)、盐酸浓度(5-25 mg L - 1)和反应温度等关键操作参数对反应的影响。在最佳条件下(HCQ = 10 mg L - 1, [H2O2] = 13 mM, scoria用量= 0.5 g L - 1,温度= 24℃),最大去除率为98%。动力学分析表明,降解符合准二阶模型。这些研究结果表明,矿渣是一种有效且低成本的fenton降解水中药物污染物的催化剂。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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