壳聚糖涂层气相二氧化硅对稀土金属离子的同时吸附:特性、动力学和等温线研究

Nurul Amirah Abd Aziz, Zul Adlan Mohd Hir, Wan Khaima Azira Wan Mat Khalir, Waheeba Ahmed Al-Amrani, Megat Ahmad Kamal Megat Hanafiah
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引用次数: 0

摘要

本研究制造并利用壳聚糖涂层气相二氧化硅复合材料(CS@silica)同时吸附水溶液中的稀土元素(REEs),包括 Ce(III)、La(III)和 Nd(III)阳离子。使用 CHNOS 分析仪、Brunauer-Emmett-Teller(BET)比表面积分析仪、衰减全反射傅立叶变换红外(ATR-FTIR)分光光度计、扫描电子显微镜耦合能量色散 X 射线(SEM-EDX)分光光度计和 X 射线衍射(XRD)分析仪对 CS@silica 复合材料进行了表征。研究结果表明,CS@二氧化硅复合材料没有孔隙,比表面积为 1.27 m 2 /g。此外,还观察到该复合材料含有大量的氧原子和氮原子,它们是吸附 REEs 的活性位点。在最佳实验条件下测定了 Ce(III)、La(III)和 Nd(III)阳离子的最大吸附容量。这些参数包括 pH 值为 4、吸附剂剂量为 0.01 克、平衡时间为 20 分钟。对 Ce(III)、La(III) 和 Nd(III) 阳离子的最大吸附容量分别为 341、241 和 299 毫克/克。吸附动力学遵循伪二阶动力学模型。在去离子水和盐酸(0.01 和 0.02 M)中,REEs 负载 CS@silica 复合材料的解吸率明显较低。这表明 REEs 与复合材料表面的活性位点之间存在化学作用。提出的主要吸附过程是络合作用,离子交换和静电接触作用较小。CS@silica 复合材料具有快速吸附和高吸附容量的特点,因此在回收 REEs 方面大有可为。
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Simultaneous Adsorption of Rare Earth Metal Ions on Chitosan-coated Fumed Silica: Characterization, Kinetics, and Isotherm Studies
The present study manufactured and utilized the chitosan-coated fumed silica composite (CS@silica) for simultaneous adsorption of rare earth elements (REEs) of Ce(III), La(III), and Nd(III) cations in an aqueous solu - tion. The CS@silica composite underwent characterization using a CHNOS analyzer, Brunauer-Emmett-Teller (BET) surface area analyzer, attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectrophotom - eter, scanning electron microscope coupled with energy-dispersive X-ray (SEM-EDX) spectrophotometer, and X-ray diffraction (XRD) analyzer. The findings indicated that the CS@silica composite exhibited a lack of pores and possessed a specific surface area of 1.27 m 2 /g. Additionally, it was observed that the composite contained a significant amount of oxygen and nitrogen atoms, which serve as the active sites for the adsorption of REEs. The maximum adsorption capacities of Ce(III), La(III), and Nd(III) cations were determined under optimal experimen - tal conditions. These parameters included a pH of 4, an adsorbent dose of 0.01 g, and an equilibrium duration of 20 min. The maximum adsorption capacities for Ce(III), La(III), and Nd(III) cations were found to be 341, 241, and 299 mg/g, respectively. The adsorption kinetics followed the pseudo-second-order kinetic model. The desorption percentage of REEs-loaded CS@silica composite was significantly low when exposed to deionized water and hydrochloric acid (0.01 and 0.02 M). This suggests that there is a chemical interaction between the REEs and the active site on the surface of the composite. The predominant adsorption process proposed was complexation, with ion exchange and electrostatic contact playing a minor role. The CS@silica composite is highly promising for the recovery of REEs because of its rapid adsorption and high adsorption capacities.
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