Adsorptive removal of methyl orange dye in aqueous solutions using calix[4]arene-modified lead sulphide: insight into response surface methodology, isotherm and kinetic studies

IF 2.1 4区 环境科学与生态学 Q2 ENGINEERING, CIVIL
Nor Zida Rosly, Abdul Halim Abdullah, Mazliana Ahmad Kamarudin, Siti Efliza Ashari, Shahrul Alang Ahmad
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引用次数: 0

Abstract

Abstract The present study reports the adsorptive potential of an alternative and regenerative adsorbent, lead sulphide (PbS) modified with calix[4]arene towards a methyl orange (MO) dye solution. The chemical and morphological aspects of synthesised PbS nanoparticles and calix[4]arene-modified PbS were analysed by FESEM, EDX and FTIR, which indicated successful immobilisation of calix[4]arene on the PbS surface. The response surface methodology (RSM), based on central composite design (CCD), was conducted to evaluate the significant factors and to optimise the influence of various factors (adsorbent dosage, contact time and pH) on the adsorption of MO. Under optimal conditions (pH of 4, a dosage of 89.70 mg and a contact time of 129.76 min), the maximum adsorption of MO by calix[4]arene-modified PbS was observed. The MO uptake behaviour was well described by the Freundlich model and the pseudo-second-order kinetic model, indicating a multilayer chemical adsorption with a maximum adsorption capacity (qmax) of 3.268 mg/g. The adsorption mechanism of MO dye on the surface of calix[4]arene-modified PbS can be attributed to various interactions such as dipole–dipole hydrogen bonding interactions, Yoshida hydrogen bonding, π–π interactions and electrostatic interaction. The results strongly demonstrated the use of novel adsorbents, calix[4]arene-modified PbS and a reusability strategy as an alternative adsorbent in MO dye removal.
用杯[4]芳烃修饰的硫化铅吸附去除水溶液中的甲基橙染料:对响应面方法、等温线和动力学研究的见解
摘要:本研究报道了一种替代再生吸附剂,杯[4]芳烃改性的硫化铅(PbS)对甲基橙(MO)染料溶液的吸附潜力。通过FESEM, EDX和FTIR分析了合成的PbS纳米颗粒和杯[4]芳烃修饰的PbS的化学和形态学方面,表明杯[4]芳烃成功地固定在PbS表面。以中心复合设计(CCD)为基础,采用响应面法(RSM)对各因素(吸附剂用量、接触时间和pH)对MO吸附的影响进行了评价和优化。在最佳条件下(pH = 4、接触时间为89.70 mg、接触时间为129.76 min),观察到杯[4]芳烃改性PbS对MO的最大吸附量。Freundlich模型和拟二级动力学模型很好地描述了MO的吸附行为,表明其为多层化学吸附,最大吸附量(qmax)为3.268 mg/g。MO染料在杯[4]芳烃修饰的PbS表面的吸附机理可归结为多种相互作用,如偶极-偶极氢键相互作用、吉田氢键相互作用、π -π相互作用和静电相互作用。结果有力地证明了新型吸附剂,杯[4]芳烃改性PbS和可重复使用策略作为MO染料去除的替代吸附剂的使用。
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来源期刊
CiteScore
4.10
自引率
21.10%
发文量
0
审稿时长
20 weeks
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