4.7 Article

Characterization of anion-cationic surfactants modified montmorillonite and its application for the removal of methyl orange

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 171, Issue 3, Pages 1150-1158

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2011.05.013

Keywords

Montmorillonite; Modification; Adsorption; Surfactant; Clay

Funding

  1. Fundamental Research Funds for the Central Universities [2010ZY37]
  2. National Laboratory of Mineral Materials [09A003]
  3. College Student Research Innovation Program
  4. Teaching Experimental Center of China University of Geosciences, Beijing

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Anion-cationic, anionic and cationic surfactants modified montmorillonite (MMT) are prepared by incorporating cationic surfactants cetyl trimethyl ammonium bromide (CTMAB), anionic surfactants sodium stearate (SSTA) and their mixture to montmorillonite. The modified samples are characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and Thermogravimetry-differential thermal analysis (TG-DTA). XRD result shows that both the anionic and cationic surfactants can be intercalated into the MMT, making the interlayer spaces of MMT expand. TG-DTA studies indicate the organic carbon contents of anion-cationic surfactants modified MMT are higher than the montmorillonite modified by anionic or cationic surfactants solely. The adsorption experiments indicate that CTMAB/10SSTA-MMT had the largest adsorption capacity compared with CTMAB-MMT and 10SSTA-MMT due to the formation of a highly effective partition medium by anion-cationic surfactant micelle. The adsorption kinetic of methyl orange onto the modified MMT samples can be best described by the pseudo-second-order model, and the adsorption isotherm is in good agreement with the Langmuir equation. The activation energy, change of free energy, enthalpy and entropy of anion-cationic modified MMT are also evaluated for the adsorption of methyl orange. Thermodynamic results indicate that the adsorption is a spontaneous and exothermic process. (C) 2011 Elsevier B.V. All rights reserved.

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