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Effect of Water on the Adsorption of Methane and Carbon Dioxide in Zeolite Na-ZSM‑5 Studied Using <i>in Situ</i> ATR-FTIR Spectroscopy
Methane
is the main component in biogas and natural gas along with
contaminants such as water and carbon dioxide. Separation of methane
from these contaminants is therefore an important step in the upgrading
process. Zeolite adsorbents and zeolite membranes have great potential
to be cost-efficient candidates for upgrading biogas and natural gas,
and in both of these applications, knowing the nature of the competitive
adsorption is of great importance to further develop the properties
of the zeolite materials. The binary adsorption of methane and carbon
dioxide in zeolites has been studied to some extent, but the influence
of water has been much less studied. In the present work, <i>in situ</i> ATR (attenuated total reflection)–FTIR (Fourier
transform infrared) spectroscopy was used to study the adsorption
of water/methane and water/carbon dioxide from binary mixtures in
a high-silica Na-ZSM-5 zeolite film at various gas compositions and
temperatures. Adsorbed concentrations for all species were determined
from the recorded IR spectra, and the experimental values were compared
to values predicted using the ideal adsorbed solution theory (IAST).
At lower temperatures (35, 50, and 85 °C), the IAST was able
to predict the binary adsorption of water and methane, whereas the
values predicted by the IAST deviated from the experimental data at
the highest temperature (120 °C). For the binary adsorption of
water and carbon dioxide, the IAST could not predict the adsorption
values accurately. This discrepancy was assigned to the particular
adsorption behavior of water in high-silica MFI forming clusters at
hydrophilic sites. However, the predicted values did follow the same
trend as the experimental values. The adsorption selectivity was determined,
and it was found that the H<sub>2</sub>O/CH<sub>4</sub> adsorption
selectivity was decreasing with increasing water content in the gas
phase at low temperatures whereas the selectivity was increasing at
higher temperatures. The H<sub>2</sub>O/CO<sub>2</sub> adsorption
selectivity was increasing with increasing water content at all temperatures