Ammonia with toxic and corrosive
features needs advanced protective
materials and removal tools, although it is a vital component in human
food supply processes. So, to satisfy these requirements, materials
with high adsorption capacity and affinity for ammonia should be developed.
The present research has been focused on a series zinc-based metal–organic
frameworks (MOF) containing mixed ligands, biphenyl dicarboxylic acid
(BPDA) and tris(4-(4H-1,2,4-triazol-4-yl)phenyl)amine
(TTPA), which are modulated by different anions including CH3COO–, CF3COO–, and
CF3SO3
–. Ammonia uptake capacity
was measured via static and dynamic conditions under 50% relative
humidity. Among all compounds, CF3SO3
– anion could enhance the ammonia uptake capacity of MOFs up to 177.85
and 349 mg/g during static and breakthrough measurements, respectively,
so that 83.30% of the total uptake capacity (at P/P
o = 1.0 and 298 K) was achieved at
low relative pressure range (up to 0.1). The isosteric heats of ammonia
adsorption on PFC-27 and derivatives were calculated in the range
of 7.03–10.16 kJ mol–1 so that they increased
upon CF3SO3
–, CF3COO–, and CH3COO– ion
incorporation. This is potentially beneficial for enhanced ammonia
adsorption. Interestingly, adsorption capacities were retained with
only slight changes after five cycles and three regeneration temperatures,
25 °C, 60 °C, and 120 °C, under vacuum. The special
affinity for NH3 adsorption and MOF phase stability after
desorption is clearly proved by FTIR spectra and PXRD analysis, respectively.
Generally, the results suggest that ion insertion modification is
an efficient strategy for enhancement of MOF adsorption performance.
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