4.8 Article

Adsorption of CO2, CH4, and N2 on Ordered Mesoporous Carbon: Approach for Greenhouse Gases Capture and Biogas Upgrading

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 47, 期 10, 页码 5474-5480

出版社

AMER CHEMICAL SOC
DOI: 10.1021/es4000643

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资金

  1. U.S. Air Force Research Laboratory [FA8650-11-C-2127]
  2. U.S. Department of Energy [DE-EE0003046]
  3. U.S. National Science Foundation [EEC 1028968]
  4. New Mexico State University Office of Vice President for Research (GREG award)
  5. Ministry of Education and Science of the Russian Federation
  6. U.S. Department of State for the Fulbright award (Distinguished Chair in Energy Conservation)

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Separation of CO2 and N-2 from CH4 is significantly important in natural gas upgrading, and capture/removal of CO2, CH4 from air (N-2) is essential to greenhouse gas emission control. Adsorption equilibrium and kinetics of CO2, CH4, and N-2 on an ordered mesoporous carbon (OMC) sample were systematically investigated to evaluate its capability in the above two applications. The OMC was synthesized and characterized with TEM, TGA, small-angle XRD, and nitrogen adsorption/desorption measurements. Pure component adsorption isotherms of CO2, CH4, and N-2 were measured at 278, 298, and 318 K and pressures up to 100 kPa, and correlated with the Langmuir model. These data were used to estimate the separation selectivities for CO2/CH4, CH4/N-2, and CO2/N-2 binary mixtures at different compositions and pressures according to the ideal adsorbed solution theory (IAST) model. At 278 K and 100 kPa, the predicted selectivities for equimolar CO2/CH4, CH4/N-2, and CO2/N-2 are 3.4, 3.7, and 12.8, respectively; and the adsorption capacities for CH4 and CO2 are 1.3 and 3.0 mmol/g, respectively. This is the first report of a versatile mesoporous material that displays both high selectivities and large adsorption capacities for separating CO2/CH4, CH4/N-2, and CO2/N-2 mixtures.

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