Highly effective removal of cobalt from aqueous solution via reusable nanocomposite of metal organic frame work and activated algae encapsulated onto double layer biopolymer

IF 5.4 3区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Communications Pub Date : 2025-05-01 Epub Date: 2025-02-23 DOI:10.1016/j.inoche.2025.114162
Amira K. Hajri , Sahr A. Alsherari , Marzough A. Albalawi , Amnah A. Alharbi , Doha A. Albalawi , Maram Qasem Albalawi
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Abstract

A significant number of researchers are focused on identifying effective methods for removing Co(II) ions from industrial wastewater. Nevertheless, current removal techniques often inadvertently eliminate other valuable metals, potentially resulting in economic disadvantages. A novel metal–organic framework has been synthesized using thorium and activated algae, encased in a double-layer hydrogel of chitosan and alginate (TMACA). Several methods were used to thoroughly characterize the adsorbent’s characteristics, such as XRD, FT-IR, XPS, FESEM, EDX, and nitrogen adsorption/desorption isotherms, to elucidate its textural characteristics. A detailed examination of nitrogen adsorption and desorption isotherms provided valuable insights into the textural characteristics of TMACA hydrogel beads. The specific surface area was quantitatively evaluated at around 1216.41 m2/g, indicating significant surface interaction potential, while the total hole volume was quantified at 0.747 cm3/g. These metrics imply that the TMACA hydrogel beads possess a notably efficient porous structure. Furthermore, the calculated average radius of particle was found to be 1.12 nm. This study analyzed how dosage, original concentration, pH, and temperature affect adsorption. The outcomes showed that the adsorption mechanism followed the pseudo-second-order model and the Langmuir isotherm. With an energy of 31.8 kJ.mol−1, chemisorption was the primary adsorption process. Higher temperatures increased metal adsorption, indicating the procedure is endothermic besides spontaneous. Through calculated tests, the adsorption process was significantly improved by using the Box-Behnken design utilising response surface methods in Design-Expert software. The study parameters included 0.02 g of TMACA hydrogel beads per 25 ml, pH of 6, and an adsorption capability of 445.8 mg/g aimed at the Co(II) solutions. The results showed that the adsorbent showed consistent stability and that its effectiveness in removing impurities did not decrease after five consecutive cycles of adsorption and desorption. Additionally, the substance maintained its initial chemical composition both before and after its reuse, demonstrated reliable effectiveness, and exhibited stable X-ray diffraction (XRD) characteristics throughout the process.

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利用可重复使用的金属有机骨架纳米复合材料和包裹在双层生物聚合物上的活化藻类,高效地去除水溶液中的钴
大量的研究人员致力于寻找去除工业废水中Co(II)离子的有效方法。然而,目前的去除技术往往会无意中去除其他有价值的金属,从而可能导致经济上的不利。用壳聚糖和海藻酸盐(TMACA)双层水凝胶包裹钍和活化藻类,合成了一种新型的金属有机骨架。采用XRD、FT-IR、XPS、FESEM、EDX、氮气吸附/脱附等温线等方法对吸附剂进行了全面表征,以阐明其结构特征。氮吸附和解吸等温线的详细检查为TMACA水凝胶珠的结构特性提供了有价值的见解。定量评价的比表面积约为1216.41 m2/g,表明明显的表面相互作用潜力,而总孔体积量化为0.747 cm3/g。这些指标表明,TMACA水凝胶珠具有显著有效的多孔结构。计算得到的粒子平均半径为1.12 nm。本研究分析了投加量、初始浓度、pH和温度对吸附的影响。结果表明,吸附机理符合拟二阶模型和Langmuir等温线。能量为31.8 kJ。Mol−1,化学吸附是主要吸附过程。较高的温度增加了金属的吸附,表明该过程除了自发外还是吸热的。通过计算试验,利用design - expert软件中的响应面方法,采用Box-Behnken设计可显著改善吸附过程。研究参数为每25 ml加入0.02 g TMACA水凝胶珠,pH为6,对Co(II)溶液的吸附量为445.8 mg/g。结果表明,该吸附剂在连续5次吸附和解吸循环后,具有稳定的吸附剂,其去除杂质的效果不降低。此外,该物质在重复使用前后都保持了其初始化学成分,表现出可靠的有效性,并在整个过程中表现出稳定的x射线衍射(XRD)特征。
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来源期刊
Inorganic Chemistry Communications
Inorganic Chemistry Communications 化学-无机化学与核化学
CiteScore
5.50
自引率
7.90%
发文量
1013
审稿时长
53 days
期刊介绍: Launched in January 1998, Inorganic Chemistry Communications is an international journal dedicated to the rapid publication of short communications in the major areas of inorganic, organometallic and supramolecular chemistry. Topics include synthetic and reaction chemistry, kinetics and mechanisms of reactions, bioinorganic chemistry, photochemistry and the use of metal and organometallic compounds in stoichiometric and catalytic synthesis or organic compounds.
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