Surface Modifications of Superparamagnetic Iron Oxide Nanoparticles with Polyvinyl Alcohol and Activated Charcoal as Methylene Blue Adsorbents

IF 2.6 4区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Magnetochemistry Pub Date : 2023-09-20 DOI:10.3390/magnetochemistry9090211
Linh Doan
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引用次数: 1

Abstract

As novel methylene blue adsorbents, polyvinyl alcohol and activated charcoal were used to modify the surface of superparamagnetic iron oxide nanoparticles. The adsorption capacity after 69 h was 26.50 ± 0.99–40.21 ± 1.30 mg/g, depending on the temperature (333.15, 310.15, and 298.15 K) and the initial concentration of methylene blue, which was between 0.017 and 0.020 mg/mL. Based on thermodynamics parameters, the adsorption process can be considered to be spontaneous endothermic physisorption. Kinetics studies show that the pseudo-second-order model was the best-fitted model. Adsorption isotherm studies show that the best-fitted models were the Langmuir, Langmuir, and Temkin and Pyzhev isotherm models when adsorbing MB at 333.15, 310.15, and 298.15 K, respectively.
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聚乙烯醇和活性炭作为亚甲基蓝吸附剂对超顺磁性氧化铁纳米颗粒的表面改性
聚乙烯醇和活性炭作为新型亚甲基蓝吸附剂,对超顺磁性氧化铁纳米颗粒进行了表面改性。不同温度(333.15、310.15和298.15 K)和亚甲基蓝初始浓度(0.017 ~ 0.020 mg/mL)的吸附量在69 h后的吸附量为26.50±0.99 ~ 40.21±1.30 mg/g。根据热力学参数,吸附过程可以认为是自发吸热物理吸附。动力学研究表明,拟二阶模型是最佳拟合模型。吸附等温线研究表明,在333.15、310.15和298.15 K下吸附MB时,Langmuir、Langmuir、Temkin和Pyzhev等温线模型最适合。
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来源期刊
Magnetochemistry
Magnetochemistry Chemistry-Chemistry (miscellaneous)
CiteScore
3.90
自引率
11.10%
发文量
145
审稿时长
11 weeks
期刊介绍: Magnetochemistry (ISSN 2312-7481) is a unique international, scientific open access journal on molecular magnetism, the relationship between chemical structure and magnetism and magnetic materials. Magnetochemistry publishes research articles, short communications and reviews. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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