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首页> 外文期刊>Chemical Engineering Communications >Oxidation-precipitation of magnetic Fe3O4/AC nanocomposite as a heterogeneous catalyst for electro-Fenton treatment
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Oxidation-precipitation of magnetic Fe3O4/AC nanocomposite as a heterogeneous catalyst for electro-Fenton treatment

机译:磁性Fe3O4 / Ac纳米复合材料的氧化沉淀为电芬顿治疗的非均相催化剂

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The oxidation-precipitation method was used for the synthesis of Fe3O4/AC. The characterization of the catalyst was accomplished by XRD, FT-IR, FE-SEM, BET, and VSM techniques. The obtained results indicated that magnetite nanoparticles were successfully prepared with cubic spinel structures and uniform distribution on the surface of activated carbon by the oxidation-precipitation method. The effect of operating parameters was evaluated to determine the optimum operating condition for the electro-Fenton (EF) removal of catechol as a phenolic pollutant model. At the optimum operating conditions (pH 3, Fe3O4/AC: 0.9 g L-1, Catechol: 8.0 x 10(-4 )mol L-1 at I: 120 mA), the catechol and COD removal reached 98.2 and 76.1% in 120 min, respectively. Only 2.1% of ferrous and 3.44% of ferric ions were leached into the solution. Regarding the results from utilization of oxidant scavengers (isopropanol and BQ), it can be inferred that hydroxyl radical (responsible for 57% catechol removal) and superoxide anion radical (responsible for 40% catechol removal) is the main oxidants in acidic (pH 3) and basic (pH 10) conditions, respectively. The kinetics of EF removal of catechol was studied and the rate constant for the pseudo-first-order kinetic model was found to be 3.37 x 10(-2)min(-1) (R-2 = 0.9924). The GC-MS analysis was carried out to detect the intermediate products and a possible degradation mechanism was proposed. The reusability of Fe3O4/AC was examined for six cycles. It can be concluded that Fe3O4/AC is an applicable ultimate catalyst for EF removal of organic pollutants.
机译:氧化沉淀法用于合成Fe3O4 / Ac。催化剂的表征是通过XRD,FT-IR,Fe-SEM,BET和VSM技术完成的。所得结果表明,通过立方尖晶石结构成功制备磁铁矿纳米颗粒,通过氧化沉淀法通过立方尖晶石结构和均匀的活性炭表面分布。评价操作参数的效果以确定用于酚醛污染物模型的电气芬顿(EF)去除儿茶酚的最佳操作条件。在最佳操作条件下(pH 3,Fe3O4 / Ac:0.9g L-1,儿茶酚:8.0×10(-4)mol L-1在I:120 mA),儿茶酚和COD去除达到98.2和76.1%分别120分钟。仅浸入溶液中仅2.1%的黑色金属铬铁和3.44%的铁离子。关于利用氧化剂清除剂(异丙醇和BQ)的结果,可以推断出羟基自由基(负责57%的儿茶酚除去)和超氧化物阴离子(负责40%儿茶酚除去)是酸性的主要氧化剂(pH3 )分别和基本(pH10)条件。研究了EF除去儿茶酚的动力学,发现伪一阶动力学模型的速率常数为3.37×10( - 2)分钟(-1)(R-2 = 0.9924)。进行GC-MS分析以检测中间产物,提出了一种可能的降解机制。检查Fe3O4 / Ac的可重用性六个周期。可以得出结论,Fe3O4 / AC是一种适用的终极催化剂,用于EF去除有机污染物。

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