4.8 Article

SO2/NO2 Separation Driven by NO2 Dimerization on SSZ-13 Zeolite Membrane

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 15, Pages 6687-6691

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c01635

Keywords

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Funding

  1. National Natural Science Foundation of China [21808012, 21971035]
  2. National Key R&D Program of China [2017YFC0210302]
  3. Fundamental Research Funds for the Central Universities [FRFIDRY-19-025, QNXM20210028]

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This study reports a method of facilitating SO2/NO2 separation through NO2 dimerization. The NO2 dimerization is triggered by temperature and pressure, resulting in N2O4 with a larger molecular size, which inhibits N2O4 diffusion into the zeolite pore and achieves high separation selectivity. High performance SO2/NO2 separation was achieved on an SSZ-13 zeolite membrane.
The molecular state is crucial for precise gas separation using a zeolite membrane, yet the state control remains a big challenge. Herein, we report a NO2 dimerization facilitated high performance SO2/NO2 separation on a SSZ-13 zeolite membrane. The NO2 dimerization is triggered by temperature and pressure to form N2O4 with big molecular size, and N(2)O(4 )diffusion into the zeolite pore is inhibited on the basis of size exclusion, leading to high separation selectivity. Consequently, SO2 rather than NO2 preferentially permeates through the SSZ-13 membrane with a high SO(2 )permeance of 2 x 10(-7 )mol m(-2) s(-1) Pa-1 and high SO2/NO2 separation factor of 22, similar to 50-fold of that measured without dimerization. The dimerization effect for SO2/NO2 separation prevails in other small-pore zeolites such as NaA. This advanced function is revealed through membrane separation using single and mixture gases.

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