4.8 Article

Probing the intermolecular interaction mechanisms between humic acid and different substrates with implications for its adsorption and removal in water treatment

Journal

WATER RESEARCH
Volume 176, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2020.115766

Keywords

Humic acid (HA); Natural organic matter (NOM); Chemical force microscopy (CFM); DLVO theory; Adhesion energy; Magnetic APTES/Fe3O4 nanoparticles

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Foundation for Innovation (CFI)
  3. Alberta Advanced Education & Technology Small Equipment Grants Program (AET/SEGP)
  4. Canada Research Chairs Program
  5. NSERC

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Humic substance is a ubiquitous class of natural organic matter (NOM) in soil and aquatic ecosystems, which severely affects the terrestrial and aquatic environments as well as water-based engineering systems by adsorption on solids (e.g., soil minerals, nanoparticles, membranes) via different interaction mechanisms. Herein, the chemical force microscopy (CFM) technique was employed to quantitatively probe the intermolecular forces of humic acid (HA, a representative humic substance) interacting with self-assembled monolayers (SAMs, i.e., OH-SAMs, CH3-SAMs, NH2-SAMs and COOH-SAMs) in various aqueous environments at the nanoscale. The interaction forces measured during approach could be well fitted by the extended Derjaguin-Landau-Verwey-Overbeek (DLVO) theory by incorporating the hydrophobic interaction. The average adhesion energy followed the trend as: NH2-SAMs (similar to 3.11 mJ/m(2)) > CH3-SAMs ;(similar to 2.03 mJ/m(2)) > OH-SAMs (similar to 1.38 mJ/m(2)) > COOH-SAMs (similar to 0.52 mJ/m(2)) in 100 mM NaCl at pH 5.8, indicating the significant role of electrostatic attraction in contributing to the HA adhesion, followed by hydrophobic interaction and hydrogen bonding. The adhesion energy was found to be dependent on NaCl concentration, Ca2+ addition and pH. For the interaction between NH2-SAMs and HA, their electrostatic attraction at pH 5.8 turned to repulsion under alkaline condition which led to the sudden drop of adhesion energy. Such results promised the adsorption and release of HA using the recyclable magnetic Fe3O4 nanoparticles coated with (3-aminopropyl)tiethoxysilane (APTES). This work provides quantitative information on the molecular interaction mechanism underlying the adsorption of HA on solids of varying surface chemistry at the nanoscale, with useful implications for developing effective chemical additives to remove HA in water treatment and many other engineering processes. (C) 2020 Elsevier Ltd. All rights reserved.

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