Affiliations 

  • 1 Univ. Savoie, LCME, F-73000 Chambéry, France; Pakistan Institute of Engineering and Applied Sciences (PIEAS), P.O. Nilore, Islamabad 45650, Pakistan
  • 2 Univ. Savoie, LCME, F-73000 Chambéry, France. Electronic address: [email protected]
  • 3 Univ. Savoie, LCME, F-73000 Chambéry, France; Fundamental and Applied Sciences Department, Universiti Teknology Petronas, Bandar Seri Iskandar, 31750 Tronoh, Malaysia
  • 4 Univ. Savoie, LCME, F-73000 Chambéry, France
  • 5 Pakistan Institute of Engineering and Applied Sciences (PIEAS), P.O. Nilore, Islamabad 45650, Pakistan
J Environ Manage, 2014 Nov 1;144:108-17.
PMID: 24929502 DOI: 10.1016/j.jenvman.2014.05.005

Abstract

The adsorption from aqueous solution of imidazolium, pyrrolidinium and pyridinium based bromide ionic liquids (ILs) having different alkyl chain lengths was investigated on two types of microporous activated carbons: a fabric and a granulated one, well characterized in terms of surface chemistry by "Boehm" titrations and pH of point of zero charge measurements and of porosity by N2 adsorption at 77 K and CO2 adsorption at 273 K. The influence of cation type, alkyl chain length and adsorbate size on the adsorption properties was analyzed by studying kinetics and isotherms of eight different ILs using conductivity measurements. Equilibrium studies were carried out at different temperatures in the range [25-55 °C]. The incorporation of ILs on the AC porosity was studied by N2 adsorption-desorption measurements at 77 K. The experimental adsorption isotherms data showed a good correlation with the Langmuir model. Thermodynamic studies indicated that the adsorption of ILs onto activated carbons was an exothermic process, and that the removal efficiency increased with increase in alkyl chain length, due to the increase in hydrophobicity of long chain ILs cations determined with the evolution of the calculated octanol-water constant (Kow). The negative values of free energies indicated that adsorption of ILs with long chain lengths having hydrophobic cations was more spontaneous at the investigated temperatures.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.