4.6 Article

Phase Transition and Criticality of Methane Confined in Nanopores

Journal

LANGMUIR
Volume 38, Issue 6, Pages 2046-2054

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.1c02955

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0021318]
  2. U.S. Department of Energy (DOE) [DE-SC0021318] Funding Source: U.S. Department of Energy (DOE)

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For the first time, the phase transition and criticality of methane confined in nanoporous media were measured and successfully predicted using an experimental setup and a self-consistent equation of state.
For the first time, the phase transition and criticality of methane confined in nanoporous media are measured. The measurement is performed by establishing an experimental setup utilizing a differential scanning calorimeter capable of operating under very low temperatures as well as high pressures to detect the capillary phase transition of methane inside nanopores. By performing experiments along isochoric cooling paths, both the capillary condensation and the bulk condensation of methane are detected. The pore critical point of nanoconfined methane is also determined and then used to derive the parameters of a previously developed self-consistent equation of state based on the generalized van der Waals partition function. Using these parameters, the equation of state can predict the capillary-condensation curves that agree well with the experimental data.

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