Affiliations 

  • 1 Department of Civil Engineering, University of Malaya, Kuala Lumpur 50603, Malaysia; University of Malaya Centre for Ionic Liquids, University Malaya, Kuala Lumpur 50603, Malaysia
  • 2 University of Malaya Centre for Ionic Liquids, University Malaya, Kuala Lumpur 50603, Malaysia; Nanotechnology & Catalysis Research Centre (NANOCAT), IPS Building, University of Malaya, 50603 Kuala Lumpur, Malaysia; National Chair of Materials Science and Metallurgy, University of Nizwa, Oman. Electronic address: mdsd68j@gmail.com
  • 3 Civil Engineering Department, Faculty of Engineering, Technology and Built Environment, UCSI University, Kuala Lumpur 56000, Malaysia
  • 4 School of Energy, Geoscience, Infrastructure and Society (EGIS), Heriot-Watt University Malaysia, 62200 Putrajaya, Malaysia
  • 5 University of Malaya Centre for Ionic Liquids, University Malaya, Kuala Lumpur 50603, Malaysia; Department of Chemical Engineering, University of Malaya, Kuala Lumpur 50603, Malaysia
J Colloid Interface Sci, 2017 07 01;497:413-421.
PMID: 28314146 DOI: 10.1016/j.jcis.2017.03.014

Abstract

Due to the interestingly tolerated physicochemical properties of deep eutectic solvents (DESs), they are currently in the process of becoming widely used in many fields of science. Herein, we present a novel Hg(2+) adsorbent that is based on carbon nanotubes (CNTs) functionalized by DESs. A DES formed from tetra-n-butyl ammonium bromide (TBAB) and glycerol (Gly) was used as a functionalization agent for CNTs. This novel adsorbent was characterized using Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy, XRD, FESEM, EDX, BET surface area, and Zeta potential. Later, Hg(2+) adsorption conditions were optimized using response surface methodology (RSM). A pseudo-second order model accurately described the adsorption of Hg(2+). The Langmuir and Freundlich isotherm models described the absorption of Hg(2+) on the novel adsorbent with acceptable accuracy. The maximum adsorption capacity was found to be 177.76mg/g.

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