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Title: | Selective and Recyclable Congo Red Dye Adsorption by Spherical Fe3O4 Nanoparticles Functionalized with 1,2,4,5-Benzenetetracarboxylic Acid |
Authors: | Chatterjee, Sobhan Guha, Nikita Krishnan, Sarathkumar Singh, Amrendra Kumar Mathur, Pradeep Rai, Dhirendra Kumar |
Issue Date: | 2020 |
Publisher: | Nature Research |
Citation: | Chatterjee, S., Guha, N., Krishnan, S., Singh, A. K., Mathur, P., & Rai, D. K. (2020). Selective and recyclable congo red dye adsorption by spherical Fe3O4 nanoparticles functionalized with 1,2,4,5-benzenetetracarboxylic acid. Scientific Reports, 10(1) doi:10.1038/s41598-019-57017-2 |
Abstract: | In this study, the new material Fe3O4@BTCA has been synthesized by immobilization of 1,2,4,5-Benzenetetracarboxylic acid (BTCA) on the surface of Fe3O4 NPs, obtained by co-precipitation of FeCl3.6H2O and FeCl2.4H2O in the basic conditions. Characterization by P-XRD, FE-SEM, and TEM confirm Fe3O4 has a spherical crystalline structure with an average diameter of 15 nm, which after functionalization with BTCA, increases to 20 nm. Functionalization also enhances the surface area and surface charge of the material, confirmed by BET and zeta potential analyses, respectively. The dye adsorption capacity of Fe3O4@BTCA has been investigated for three common dyes; Congo red (C.R), Methylene blue (M.B), and Crystal violet (C.V). The adsorption studies show that the material rapidly and selectively adsorbs C.R dye with very high adsorption capacity (630 mg/g), which is attributed to strong H-bonding ability of BTCA with C.R dye as indicated by adsorption mechanism study. The material also shows excellent recyclability without any considerable loss of adsorption capacity. Adsorption isotherm and kinetic studies suggest that the adsorption occurs by the Langmuir adsorption model following pseudo-second-order adsorption kinetics. © 2020, The Author(s). |
URI: | https://doi.org/10.1038/s41598-019-57017-2 https://dspace.iiti.ac.in/handle/123456789/8757 |
ISSN: | 2045-2322 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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