A redox-active covalent organic framework for the efficient detection and removal of hydrazine

J Hazard Mater. 2020 Jan 5:381:120983. doi: 10.1016/j.jhazmat.2019.120983. Epub 2019 Aug 10.

Abstract

The removal and detection of soluble hydrazine is of importance due to its harm to soil and subterranean water, but challenging. Herein, we preferentially disposed a porous and redox active covalent-organic framework (DAAQ-TFP COF, denoted as DQ-COF) to simultaneously removal and detect hydrazine. Electroactive sites (anthraquinone units) can be intelligently incorporated into the channel walls/pores of COF. DQ-COF has high crystallinity and good thermal stability, and DQ-COF dropped onto nickel matrix (DQ-COF/Ni composite) still retains high surface area, characterized by PXRD, FT-IR, nitrogen adsorption and TGA. Subsequently, a detailed study of DQ-COF towards hydrazine uptake and detection potentials is explored. DQ-COF as adsorbent unfolds strong removal ability towards hydrazine, the maximum removal capacity of which is up to 1108 mg g-1, following Friedrich and pseudo-second-order kinetic models. Meanwhile, the DQ-COF supported on nickel renders attractive electrochemical properties, which is efficiently responsive to hydrazine at a part per billion (ppb) level, coupled with a wide linear range (0.5 ˜ 1223 μM), low detection limit (0.07 μM) and high anti-interference ability. There is no other COFs with such a favorable capability in synchronous removal and selective detection towards hydrazine, probably applying in superintending water quality and disposing wastewater.

Keywords: Covalent organic framework; Electrochemical detection; Removal.

Publication types

  • Research Support, Non-U.S. Gov't