4.7 Article

Superb adsorption capacity of hierarchical calcined Ni/Mg/Al layered double hydroxides for Congo red and Cr(VI) ions

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 321, Issue -, Pages 801-811

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhazmat.2016.09.070

Keywords

Layered double hydroxide; Hierarchical hollow sphere; Adsorption; Congo red; Cr(VI) ion

Funding

  1. NSFC [21433007, 51320105001, 51272199]
  2. 973 Program [2013CB632402]
  3. Fundamental Research Funds for the Central Universities [2015-III-034]
  4. Self-determined and Innovative Research Funds of SKLWUT [2015-ZD-1]
  5. Natural Science Foundation of Hubei Province of China [2015CFA001]

Ask authors/readers for more resources

The preparation of hierarchical porous materials as catalysts and sorbents has attracted much attention in the field of environmental pollution control. Herein, Ni/Mg/Al layered double hydroxides (NMA-LDHs) hierarchical flower-like hollow microspheres were synthesized by a hydrothermal method. After the NMA-LDHs was calcined at 600 degrees C, NMA-LDHs transformed into Ni/Mg/Al layered double oxides (NMA-LDOs), which maintained the hierarchical flower-like hollow structure. The crystal phase, morphology, and microstructure of the as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy elemental mapping, Fourier transform infrared spectroscopy, and nitrogen adsorption-desorption methods. Both the calcined and non-calcined NMA-LDHs were examined for their performance to remove Congo red (CR) and hexavalent chromium (Cr(VI)) ions in aqueous solution. The maximum monolayer adsorption capacities of CR and Cr(VI) ions over the NMA-LDOs sample were 1250 and 103.4 mg/g at 30 degrees C, respectively. Thermodynamic studies indicated that the adsorption process was endothermic in nature. In addition, the addition of coexisting anions negatively influenced the adsorption capacity of Cr(VI) ions, in the following order: CO32- > SO42- >H2PO4- > Cl-. This work will provide new insight into the design and fabrication of advanced adsorption materials for water pollutant removal. (C) 2016 Elsevier B.V. All rights reserved.

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