改性介孔沸石- a /还原氧化石墨烯纳米复合材料有效去除废水中的镉离子:动力学和热力学研究

M. Farghali, M. Abo-aly, T. Salaheldin
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摘要

以3-氨基丙基-三甲氧基硅烷(APTMS)为介孔生成剂和交联剂,研究了改性介孔沸石-a /还原性氧化石墨烯纳米复合材料(MZ-A/RGO)去除废水中镉(Cd 2+)离子的性能。利用x射线衍射、衰减全反射-傅里叶变换红外光谱(ATR-FTIR)和场发射扫描电镜证实了MZ-A/RGO纳米复合材料的成功制备。结果表明,修饰后的介孔沸石a (MZ-A)附着在还原氧化石墨烯(RGO)纳米片表面,无任何聚集。对MZ-A/RGO进行了脱除Cd 2+的吸附处理实验,考察了不同吸附参数(接触时间、初始吸附浓度和温度)对MZ-A/RGO的吸附能力。吸附结果表明,15分钟的安静时间足以达到最大吸附量222.23 mg/g的平衡状态,实验数据符合拟二级动力学模型。等温线研究采用Langmuir模型对所得实验数据拟合最好,热力学结果证实了MZ-A/RGO纳米复合材料吸附Cd +离子的吸热性质。
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Effective removal of cadmium ions from wastewater using modified mesoporous zeolite-A /reduced graphene oxide nanocomposite: kinetic and thermodynamic studies
This study discusses the capability of the prepared modified mesoporous zeolite-A /reduced graphene oxide nanocomposite (MZ-A/RGO) in removal of cadmium (Cd 2+ ) ions from wastewater, in which 3-aminopropyl- trimethoxysilane (APTMS) was used as a mesopore generating and cross linkage agent in this preparation. X-ray diffraction, attenuated total reflectance- Fourier transform infrared spectroscopy (ATR-FTIR) and field emission scanning electron microscope were used to confirm the successful preparation of MZ-A/RGO nanocomposite. The results indicated that the modified mesoporous zeolite-A (MZ-A) was attached to the surface of the reduced graphene oxide (RGO) nanosheets without any aggregation. The adsorption treatment experiments were conducted for Cd 2+ ions removal and the adsorption capacities of MZ-A/RGO were determined under different adsorption parameters including, the contact time, initial adsorbate concentrations and temperature. The adsorption results revealed that 15 minutes was quiet enough to ensure the equilibrium state with maximum adsorption capacity 222.23 mg/g and the experimental data was fitted well with the pseudo-second-order kinetic model. The isotherm studies refer to the Langmuir model exhibits best fitting for the obtained experimental data and the thermodynamic results confirm that the endothermic nature of the adsorption of Cd 2+ ions on MZ-A/RGO nanocomposite.
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