Transition metal cation-exchanged SSZ-13 zeolites for CO2 capture and separation from N2

Mingzhe Sun (Co-first Author), Qinfen Gu (Co-first Author), Aamir Hanif, Tianqi Wang, Jin Shang*

*Corresponding author for this work

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

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Abstract

CO2 capture from post-combustion flue gas mixture (CO2/N2:15/85) is challenging and requires adsorbents with high capacity and high selectivity toward CO2. Our work validated the potential of transition metal cation-exchanged SSZ-13 zeolites for efficient CO2 capture, as evaluated by unary static isothermal adsorption and binary dynamic column breakthrough experiments as well as predicted performance in pressure/vacuum swing adsorption (P/VSA) process. Among the investigated transition metals (Co(II), Ni(II), Zn(II), Fe(III), Cu(II), Ag(I), La(III), and Ce(III)) exchanged SSZ-13, Co(II)/SSZ-13 and Ni(II)/SSZ-13 showed the highest CO2 uptake (4.49 and 4.45 mmol/g, respectively) and superior selectivity of CO2 over N2 (52.55 and 42.61, respectively) at 273 K and 1 atm. We attribute such outstanding separation performance to the Pi backdonation exclusively formed between CO2 and transition metal cation sites. This demonstrates a new approach of developing adsorbents for CO2 capture in the real-world industrial processes.
Original languageEnglish
Pages (from-to)1450-1458
JournalChemical Engineering Journal
Volume370
Online published26 Mar 2019
DOIs
Publication statusPublished - 15 Aug 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 9 - Industry, Innovation, and Infrastructure
    SDG 9 Industry, Innovation, and Infrastructure
  2. SDG 13 - Climate Action
    SDG 13 Climate Action

Research Keywords

  • Adsorption
  • CO2 capture
  • Zeolites

Publisher's Copyright Statement

  • COPYRIGHT TERMS OF DEPOSITED POSTPRINT FILE: © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/

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