Fuller’s Earth–immobilized FeS nanoparticles for efficient adsorption of crystal violet in aqueous solution

IF 2.1 4区 材料科学 Q3 CHEMISTRY, MULTIDISCIPLINARY Journal of Nanoparticle Research Pub Date : 2024-09-21 DOI:10.1007/s11051-024-06128-7
Khadim Hussain, Amarjeet Dahiya, Akanksha Bhardwaj, Archana Rani, Meenu Arora, J. Nagendra Babu
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Abstract

FeS@Fuller’s Earth (FeS@FE) was synthesized by borohydride reduction in presence of dithionite with a 10% w/w iron loading. FESEM analysis reveal immobilized FeS NPs (40–100 nm) on the surface of Fuller’s Earth with agglomeration. The presence of sulfur as confirmed from XPS and EDX analysis of FeS@FE. Batch adsorption study of FeS@FE for crystal violet (CV) dye adsorption in aqueous solution yielded an optimized adsorption at pH 8, adsorbent dose 0.1 g/L, with a removal of upto 80% of the dye from a 20 mg/L CV solution. The CV adsorption on FeS@FE followed a good non-linear fit for Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich isotherm with R2 > 0.95. The maximum monolayer adsorption capacity of FeS@FE was found to be 601.2 mg/g for CV with a D-R Isotherm Free energy of 141.58 kJ/mol at optimum conditions of pH 8, 100 mg/L of CV, and 0.1 g/L of adsorbent dose. The non-linear kinetic fit for CV dye adsorption on FeS@FE fitted to the pseudo-second-order (PSO) and intraparticle diffusion (IPD) models, indicating a strong chemical interaction between CV and FeS@FE. The strong adsorption of CV using FeS@FE is attributed to the Fe-OOH surface formation by FeS immobilized on FE under alkaline conditions, leading to deprotonation and electrostatic adsorption of the dye.

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富勒土固定化 FeS 纳米粒子在水溶液中高效吸附水晶紫
FeS@Fuller's Earth(FeS@FE)是在含铁量为 10% w/w 的二亚硫酸盐存在下通过硼氢化还原法合成的。FESEM 分析表明,富勒土表面有固定的 FeS NPs(40-100 nm),并有团聚现象。对 FeS@FE 的 XPS 和 EDX 分析证实了硫的存在。对 FeS@FE 在水溶液中吸附水晶紫(CV)染料的批量吸附研究表明,在 pH 值为 8、吸附剂剂量为 0.1 克/升时,吸附效果最佳,20 毫克/升 CV 溶液中的染料去除率高达 80%。CV在FeS@FE上的吸附与Langmuir、Freundlich、Temkin和Dubinin-Radushkevich等温线呈良好的非线性拟合,R2为0.95。在 pH 值为 8、CV 为 100 mg/L 和吸附剂剂量为 0.1 g/L 的最佳条件下,FeS@FE 对 CV 的最大单层吸附容量为 601.2 mg/g,D-R 等温线自由能为 141.58 kJ/mol。CV染料在FeS@FE上吸附的非线性动力学拟合符合伪二阶(PSO)和颗粒内扩散(IPD)模型,表明CV与FeS@FE之间存在很强的化学作用。FeS@FE 对 CV 的强吸附作用是由于固定在 FE 上的 FeS 在碱性条件下形成了 Fe-OOH 表面,导致染料的去质子化和静电吸附。
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来源期刊
Journal of Nanoparticle Research
Journal of Nanoparticle Research 工程技术-材料科学:综合
CiteScore
4.40
自引率
4.00%
发文量
198
审稿时长
3.9 months
期刊介绍: The objective of the Journal of Nanoparticle Research is to disseminate knowledge of the physical, chemical and biological phenomena and processes in structures that have at least one lengthscale ranging from molecular to approximately 100 nm (or submicron in some situations), and exhibit improved and novel properties that are a direct result of their small size. Nanoparticle research is a key component of nanoscience, nanoengineering and nanotechnology. The focus of the Journal is on the specific concepts, properties, phenomena, and processes related to particles, tubes, layers, macromolecules, clusters and other finite structures of the nanoscale size range. Synthesis, assembly, transport, reactivity, and stability of such structures are considered. Development of in-situ and ex-situ instrumentation for characterization of nanoparticles and their interfaces should be based on new principles for probing properties and phenomena not well understood at the nanometer scale. Modeling and simulation may include atom-based quantum mechanics; molecular dynamics; single-particle, multi-body and continuum based models; fractals; other methods suitable for modeling particle synthesis, assembling and interaction processes. Realization and application of systems, structures and devices with novel functions obtained via precursor nanoparticles is emphasized. Approaches may include gas-, liquid-, solid-, and vacuum-based processes, size reduction, chemical- and bio-self assembly. Contributions include utilization of nanoparticle systems for enhancing a phenomenon or process and particle assembling into hierarchical structures, as well as formulation and the administration of drugs. Synergistic approaches originating from different disciplines and technologies, and interaction between the research providers and users in this field, are encouraged.
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