4.6 Article

Effect of Light Gas Components on CO2 Permeation through DD3R Membranes

Journal

INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
Volume 61, Issue 49, Pages 18100-18108

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.2c03474

Keywords

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Funding

  1. National Key Research and Development Program of China [2021YFC2101203]
  2. National Natural Science Foundation of China [22035002, 22178164]
  3. Jiangsu Provincial Carbon Peak Carbon Neutral Science and Technology Innovation Special Fund [BE2022033]
  4. Jiangsu Specially-Appointed Professors Program, State Key Laboratory of Materials-Oriented Chemical Engineering [ZK202002]

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Membrane technology is considered a promising alternative for natural gas upgrading, and zeolite membranes, known for their stability, have gained attention. This study investigated the permeation of CO2 through DD3R zeolite membranes in the presence of light gas components. The diffusion of CO2 was slightly affected by N2, CH4, and SF6, but significantly decreased in equimolar CO2/C2H6 due to competitive adsorption and slow diffusion of C2H6 molecules. An empirical formula for predicting CO2 diffusion in ternary mixtures was proposed, providing a convenient method for membrane area determination in multicomponent mixture separation.
Membrane technology has emerged to be a promising alternative for natural gas upgrading. Zeolite membranes are attracting more and more attention because of the hydro-thermal and chemical stability. However, the zeolite membranes are generally evaluated in the unary or binary CO2/CH4 components, which is far from the real applications. Herein we investigated the CO2 permeation through DD3R zeolite mem-branes under the presence of light gas components (e.g., N2, CH4, C2H6, and SF6). The CO2 diffusivity was calculated by the generalized Maxwell-Stefan model for more insights on CO2 transport. The diffusion of CO2 molecules was slightly affected by the presence of N2, CH4, and SF6. However, the CO2 diffusivity in equimolar CO2/C2H6 was one magnitude lower than that of pure CO2 component because of the strong competitive adsorption and slow diffusion of C2H6 molecules. An empirical formula was proposed to predict the CO2 diffusivity in the CO2/CH4/C2H6 ternary mixture. The predicted CO2 flux matched well with the experimental one for the mixture containing less than 15 mol % C2H6. This would provide a facile method to determine the required membrane area for multicomponent mixture separation.

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