Ionic liquids (ILs), as promising candidates for ammonia
(NH3) separation and recovery, have attracted extensive
attention
due to their extremely low pressures, high gas affinity, and adjustable
structures. However, the development of new absorbents or adsorbents
for highly efficient, fast, and reversible separation is still a great
challenge. In this work, multiproton ILs (MPILs) by simultaneously
introducing two or more −H, −OH, or −SO3H sites into the cations were designed to enhance NH3 uptake,
and the MPIL N,N,N′,N′-tetrakis (2-hydroxyethyl)ethylenediamine
trifluoromethane sulfonate ([EdteH6][TfO]2)
with four −OH and two −H sites exhibited a superhigh
capacity of 5.08 mol NH3·(mol IL)−1 at 40 °C and 1 bar. To solve the slow gas–liquid mass
transfer due to the high viscosity of MPILs, the designed MPILs were
highly dispersed onto the molecular sieve HZSM-5 with abundant pore
structures to prepare a series of porous MPIL-based hybrid adsorbents
for NH3 adsorption. The highest capacity of 140.42 mg
NH3·(g adsorbent)−1 at 30 °C
and 1 bar was achieved by 60 wt % [EdteH6][TfO]2@HZSM-5-60 (HZ60) due to multiple hydrogen bonding and mesopore effects,
which is superior to all of the nonmetal IL-based adsorbents reported
to date. Meanwhile, the 60 wt % [EdteH6][TfO]2@HZ60 also exhibited high NH3/CO2 and NH3/N2 selectivities, which are almost 16 and 14 times
greater than that of pure HZ60, respectively, along with excellent
reversibility. This work provides a feasible way to design novel porous
IL-based adsorbents for gas separation and recovery.