Issue 9, 2014

Synthesis of copper–isonicotinate metal–organic frameworks simply by mixing solid reactants and investigation of their adsorptive properties for the removal of the fluorescein dye

Abstract

The formation of [Cu(INA)2] (INA = isonicotinate) metal–organic frameworks (MOFs) by a highly efficient and environmentally benign method simply by mixing and heating solid reactants without milling has been investigated. The materials were characterized using elemental analysis, FT-IR spectroscopy and powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM). Comparison of PXRD patterns of the materials with patterns simulated from single crystal X-ray diffraction data allowed identification of the products. The adsorption properties of [Cu(INA)2] were studied using the fluorescein dye (FS). The adsorption data followed both Langmuir and Freundlich equations but was best suited to the Langmuir model. The adsorption data were also correlated with the Temkin and Dubinin–Radushkevich adsorption model and the results showed that the adsorption process is physical. These results indicate that the adsorption of FS on [Cu(INA)2] is partly due to electrostatic interaction between fluorescein and the adsorbent. Compared with the traditional synthetic techniques, this method for the synthesis of MOFs was found to be highly efficient, environmentally benign and useful for the large-scale production.

Graphical abstract: Synthesis of copper–isonicotinate metal–organic frameworks simply by mixing solid reactants and investigation of their adsorptive properties for the removal of the fluorescein dye

Supplementary files

Article information

Article type
Paper
Submitted
19 Mar 2014
Accepted
23 Jun 2014
First published
23 Jun 2014

New J. Chem., 2014,38, 4494-4500

Author version available

Synthesis of copper–isonicotinate metal–organic frameworks simply by mixing solid reactants and investigation of their adsorptive properties for the removal of the fluorescein dye

A. C. Tella, S. O. Owalude, C. A. Ojekanmi and O. S. Oluwafemi, New J. Chem., 2014, 38, 4494 DOI: 10.1039/C4NJ00411F

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