Optimization of Preparation of Fe3O4-L by Chemical Co-Precipitation and Its Adsorption of Heavy Metal Ions

吸附 吸热过程 放热反应 粒径 水溶液中的金属离子 解吸 金属 化学 摩尔比 傅里叶变换红外光谱 核化学 降水 摩尔浓度 化学工程 物理化学 催化作用 有机化学 气象学 工程类 物理
作者
Junzhen Di,Xueying Sun,Siyi Zhang,Yanrong Dong,Bofu Yuan
出处
期刊:Journal of Renewable Materials [Computers, Materials and Continua (Tech Science Press)]
卷期号:11 (5): 2209-2232
标识
DOI:10.32604/jrm.2023.025241
摘要

To address the serious pollution of heavy metals in AMD, the difficulty and the high cost of treatment, Fe3O4-L was prepared by the chemical co-precipitation method. Based on the single-factor and RSM, the effects of particle size, total Fe concentration, the molar ratio of Fe2+ to Fe3+ and water bath temperature on the removal of AMD by Fe3O4-L prepared by chemical co-precipitation method were analyzed. Static adsorption experiments were conducted on Cu2+, Zn2+ and Pb2+ using Fe3O4-L prepared under optimal conditions as adsorbents. The adsorption properties and mechanisms were analyzed by combining SEM-EDS, XRD and FTIR for characterization. The study showed that the effects of particle size, total Fe concentration and the molar ratio of Fe2+ to Fe3+ are larger. Obtained by response surface optimization analysis, the optimum conditions for the preparation of Fe3O4-L were a particle size of 250 mesh, a total Fe concentration of 0.5 mol/L, and a molar ratio of Fe2+ to Fe3+ of 1:2. Under these conditions, the removal rates of Cu2+, Zn2+, and Pb2+ were 94.52%, 88.49%, and 96.69% respectively. The adsorption of Cu2+, Zn2+ and Pb2+ by Fe3O4-L prepared under optimal conditions reached equilibrium at 180 min, with removal rates of 99.99%, 85.27%, and 97.48%, respectively. The adsorption reaction of Fe3O4-L for Cu2+ and Zn2+ is endothermic, while that for Pb2+ is exothermic. Fe3O4-L can still maintain a high adsorption capacity after five cycles of adsorption-desorption experiments. Cu2+, Zn2+ and Pb2+ mainly exist as CuFe2O4, Zn(OH)2, ZnFe2O4 and PbS after being adsorbed by Fe3O4-L, which is the result of the combination of physical diffusion, ion exchange and surface complexation reaction.
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