Effect of Direct yellow 50 removal from an aqueous solution using nano bentonite; adsorption isotherm, kinetic analysis and also thermodynamic behavior

被引:8
|
作者
Alabbad, Eman A. [1 ]
机构
[1] Imam Abdulrahman Bin Faisal Univ, Coll Sci, Dept Chem, POB 1982, Dammam 31441, Saudi Arabia
关键词
Nano bentonite; Adsorption isotherm; Kinetic studies; Direct yellow 50; Wastewater; CADMIUM ION; WATER; DYES; EQUILIBRIUM; NANOPARTICLES; ELECTROLYTE; CHITOSAN; SORPTION; NICKEL; PH;
D O I
10.1016/j.arabjc.2022.104517
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The developing countries are suffering from the toxicity of different industrial effluents, especially dyes that contaminate water systems. This study successfully explained the preparation and characterization of nano bentonite to extract Direct Yellow Fifty (DY50). Direct Yellow 50 is an organic contaminant that may affect the quality of water. The characterization of prepared nanoparticles was done using Scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier-transform infrared (FTIR). The impact of different operating conditions was studied using different pH, dose, temperature, contact time, and initial DY50 concentrations. The obtained results indicated that nano bentonite could adsorb about 94 % at initial concentrations of 40 mg/L, respectively. The optimum removal conditions were observed at an acidic pH (pH 3) using a sorbent material dosage of 0.05 g for 4 h at 30 degrees C. The adsorption isotherm, kinetic analysis, and thermo-dynamic behavior were studied using linear equation form, and the adjusted R2 was compared to detect the preferred models. The adsorption behavior pseudo-second order kinetics, and fitted Langmuir isotherm model, respectively, showed the chemisorption interactions between adsorbed and sorbed molecules. Thermodynamic behavior indicated that the reaction was exothermic. Finally, this study strongly recommended using nano bentonite for DY50 removal from an aqueous solution.(c) 2022 The Author. Published by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页数:12
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