Affiliations 

  • 1 Department of Chemistry, College of Science, King Khalid University, Abha, 61413, Saudi Arabia. Electronic address: samichemist1@gmail.com
  • 2 Department of Chemistry, College of Science, King Khalid University, Abha, 61413, Saudi Arabia
  • 3 Department of Petroleum Engineering, School of Engineering, Asia Pacific University of Technology and Innovation, 57000, Kuala Lumpur, Malaysia
  • 4 Department of Chemical Engineering, NFC Institute of Engineering and Fertilizer Research, Faisalabad, 38000, Pakistan; Department of Chemical Engineering, Universiti Teknologi PETRONAS, 32610, Perak, Malaysia
  • 5 Department of Chemical Engineering, COMSATS University Islamabad, Lahore Campus, Defense Road, Lahore, 54000, Pakistan
  • 6 Department of Chemical Engineering, Universiti Teknologi PETRONAS, 32610, Perak, Malaysia
  • 7 Department of Chemical Engineering, College of Engineering, Khalifa University, P.O. Box 127788, Abu Dhabi, United Arab Emirates
  • 8 Department of Environmental Sciences and Engineering, Government College University, Faisalabad, 38000, Punjab, Pakistan
  • 9 Department of Chemical and Environmental Engineering, University of Nottingham, Malaysia, 43500, Semenyih, Selangor Darul Ehsan, Malaysia. Electronic address: PauLoke.Show@nottingham.edu.my
Chemosphere, 2021 May;271:129504.
PMID: 33445018 DOI: 10.1016/j.chemosphere.2020.129504

Abstract

This study reports the application of hydrated lime for the effective adsorption of the heavy mercury metal from the aqueous phase solutions. Initially, hydrated lime was subjected to structural characterization and thermal stability analysis. The FT-IR spectrum analysis revealed that the existence of the O-H bonds as a confirmation of hydrated lime formation. Subsequently, the XRD powder-based analysis demonstrated that most of the hydrated lime is pure crystalline material known as Portlandite while a small amount of calcite is also present in the structure of the hydrated lime. The thermal stability analysis revealed that the hydrated lime is highly thermally stable under harsh conditions without decomposing at higher temperatures up to 500 °C. Furthermore, the hydrated lime was subjected to the selective adsorption of heavy metal mercury to investigate the potential influence of the adsorbent particle size and loading on adsorption capacity. The results demonstrated that the decrease in the adsorbent particle size leads to the improvement in the mercury adsorption attributing to the rise in specific surface area. The enhancement in the loading of the adsorbent resulted in a reduction in mercury adsorption directing to the fact that already adsorbed metal ions onto the adsorbent surface lead to hindrance for the adsorption of other ions of heavy metal. These results lead to a significant impact on modern in inventing different adsorbents with promising water treatment efficiency for more industrial applications and the related recovery of mercury.

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