Deep-eutectic-solvothermal synthesis of cerium-iron bimetallic oxides (Ce:Fe-DES) for the removal of arsenic from water

IF 5.2 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Liquids Pub Date : 2025-05-15 Epub Date: 2025-03-08 DOI:10.1016/j.molliq.2025.127326
Esmeralda Vences-Alvarez , Arturo Mendoza-Galván , J. Rene Rangel-Mendez , Gabriel Luna-Barcenas
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Abstract

This research focuses on the development of innovative adsorbent materials for the removal of arsenic (As) from contaminated waters, a critical challenge for public health worldwide. Given the growing concern about environmental impacts, there is a need to explore sustainable methods in the synthesis of these materials, replacing conventional organic solvents. In this context, deep eutectic solvents (DES) have emerged as a promising and green alternative, allowing the fabrication of metal oxides with highly specialized chemical structures and properties. In this study, the synthesis of bimetallic cerium and iron oxyhydroxides has been achieved using a choline chloride:urea DES medium, by a microwave-assisted methodology, allowing a green and more sustainable methodology, avoiding the use of toxic solvents and reducing reaction temperatures.. The resulting materials, Ce:Fe-DES, were physiochemically characterized by various techniques, and multiple parameters were evaluated. The Ce:Fe-DES adsorbent material has an As(V) adsorption capacity of 22.87 mg/g at an equilibrium concentration of 2.3 mg/l, and this decreases only 25 % in the presence of a mixture of anions with a concentration of 25 mg/l of each of the competing anions (F-, Cl-, SO42-, NO3-, PO43- and CO32-). Moreover, Ce:Fe-DES has an acceptable arsenic adsorption capacity with the advantage that it was synthesized using a green methodology that does not generate toxic waste. Also, the Ce:Fe-DES As removal remains almost constant after the second adsorption cycle and has proven to be a promising As(V) adsorbent materials because factors such as solution pH and the concentration of coexisting anions have little interference in the As(V) adsorption process.

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深共晶-溶剂热合成铈-铁双金属氧化物(Ce:Fe-DES)去除水中砷
这项研究的重点是开发用于从受污染的水中去除砷(As)的创新吸附材料,这是全球公共卫生面临的一个重大挑战。鉴于对环境影响的日益关注,有必要探索可持续的方法来合成这些材料,取代传统的有机溶剂。在这种背景下,深共晶溶剂(DES)作为一种有前途的绿色替代品出现了,它允许制造具有高度专门化化学结构和性能的金属氧化物。在本研究中,使用氯化胆碱:尿素DES介质,通过微波辅助方法,实现了双金属铈和铁氧氢氧化物的合成,允许绿色和更可持续的方法,避免使用有毒溶剂和降低反应温度。通过各种技术对所得材料Ce:Fe-DES进行了物理化学表征,并对多个参数进行了评估。Ce:Fe-DES吸附材料在平衡浓度为2.3 mg/l时,对砷(V)的吸附量为22.87 mg/g,而在竞争阴离子(F-、Cl-、SO42-、NO3-、PO43-和CO32-)浓度均为25 mg/l时,吸附量仅下降25%。此外,Ce:Fe-DES具有可接受的砷吸附能力,其优点是采用绿色方法合成,不会产生有毒废物。此外,Ce:Fe-DES在第二次吸附循环后对As的去除几乎保持不变,由于溶液pH和共存阴离子浓度等因素对As(V)吸附过程的干扰很小,被证明是一种很有前途的As(V)吸附材料。
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来源期刊
Journal of Molecular Liquids
Journal of Molecular Liquids 化学-物理:原子、分子和化学物理
CiteScore
10.30
自引率
16.70%
发文量
2597
审稿时长
78 days
期刊介绍: The journal includes papers in the following areas: – Simple organic liquids and mixtures – Ionic liquids – Surfactant solutions (including micelles and vesicles) and liquid interfaces – Colloidal solutions and nanoparticles – Thermotropic and lyotropic liquid crystals – Ferrofluids – Water, aqueous solutions and other hydrogen-bonded liquids – Lubricants, polymer solutions and melts – Molten metals and salts – Phase transitions and critical phenomena in liquids and confined fluids – Self assembly in complex liquids.– Biomolecules in solution The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include: – Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.) – Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.) – Light scattering (Rayleigh, Brillouin, PCS, etc.) – Dielectric relaxation – X-ray and neutron scattering and diffraction. Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.
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