Methane (CH) is the primary component of natural gas and must be purified to a certain level before it can be used as pipeline gas or liquified natural gas (LNG). In particular, nitrogen (N), a common contaminant in natural gas needs to be rejected to increase the heating value of the gas and meet the LNG product specifications. The development of energy-efficient N removal technologies is hampered by N's inertness and its resemblance to CH in terms of kinetic size and polarizability. N-selective materials are so rare. Here, for the first time, we screened 1425 alkali metal cation exchange zeolites to identify the candidates with the best potential for the separation of N from CH. We discovered a few extraordinary zeolite frameworks capable of achieving equilibrium selectivity toward N. Particularly, Li-RRO-3 zeolite with a specific two-dimensional structure demonstrated a selective N adsorption capacity of 2.94 mmol/g at 283 K and 1 bar, outperforming the capacity of all known zeolites. Through an density functional theory study, we found that the five-membered ring of the RRO framework is the most stable cationic site for Li, and this Li can interact with multiple N molecules but only one CH, revealing the mechanism for the high capacity and selectivity of N. This work suggests promising adsorbents to enable N rejection from CH in the gas industry without going for energy-intensive cryogenic distillations.
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http://dx.doi.org/10.1021/acs.langmuir.2c03089 | DOI Listing |
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