Skip to main navigation Skip to search Skip to main content

Mechanistic study of atenolol, acebutolol and carbamazepine adsorption on waste biomass derived activated carbon

  • Ming-Ho To
  • , Pejman Hadi
  • , Chi-Wai Hui
  • , Carol Sze Ki Lin
  • , Gordon McKay*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Palm kernel shell (PKS) was physically activated by carbon dioxide at 900 °C for 1.5 h and tested for its ability to remove Atenolol (ATE), Acebutolol (ACE) and Carbamazepine (CBM), which are pharmaceutically active compounds (PhACs). Rapid adsorption of PhACs took place in the first 90 min and reached equilibrium after 4 h. The kinetic data were best fitted by the Ritchie-second-order model and confirmed by the diffusion-chemisorption model implying a predominantly chemisorption mechanism. The isotherm adsorption studies showed that the maximum adsorption capacities of ATE, ACE and CBM were 0.69, 0.67 and 0.72 mmol/g respectively. The best fit isotherm was the Sips equation.
Original languageEnglish
Pages (from-to)386-398
JournalJournal of Molecular Liquids
Volume241
Online published10 May 2017
DOIs
Publication statusPublished - Sept 2017

Research Keywords

  • Acebutolol ACE
  • Adsorption
  • Atenolol ATE
  • Carbamazepine CBM
  • Palm kernel shell (PKS)
  • Pharmaceutically active compounds PhACs
  • Point of zero charge pHpzc

Fingerprint

Dive into the research topics of 'Mechanistic study of atenolol, acebutolol and carbamazepine adsorption on waste biomass derived activated carbon'. Together they form a unique fingerprint.

Cite this