MOFs-derived conductive structure for high-performance removal/release of phosphate as electrode material

Water Res. 2020 Oct 1:184:116198. doi: 10.1016/j.watres.2020.116198. Epub 2020 Jul 17.

Abstract

Porous metal-organic frameworks (MOFs) have drawn increasing attention as promising phosphate adsorbents. Yet the potential agglomeration of MOFs particles and the difficult collection process largely thwarted their application. Meanwhile, adsorbents regeneration might destroy MOFs structures due to the use of strong alkaline solution. In this work, we reported a strategy for designing and fabricating an electrode to remove phosphate based on MIL-101 derived metal/carbon via a two-step carbonization step, which not only introduced C doping but also created a stable structure. With the assistance of electric field, the migration and capture of phosphate anions were greatly enhanced. Under 1 V condition, the material exhibited a high maximum removal capacity of 97.73 mg P/g. Adsorption kinetics and parameters for phosphate at different conditions were analyzed. Langmuir and Freundlich isotherms were employed to validate the adsorption data. More importantly, the regeneration of electrode was achieved in a more facile and efficient way than micro/ nanoparticles adsorbents by simple voltage control. Such an intriguing approach may provide a new platform to further expand the use of MOFs for adsorption process.

Keywords: Capacitive deionization; Conductive structure; MOF-derived material; Phosphate removal; Porous morphology.

MeSH terms

  • Adsorption
  • Electrodes
  • Kinetics
  • Metal-Organic Frameworks*
  • Phosphates

Substances

  • Metal-Organic Frameworks
  • Phosphates