Several archetypical metal organic frameworks (MOFs),
namely, HKUST-1, ZIF-8, MIL-100(Al), MIL-53(Al), and NH2-MIL-53(Al), were synthesized via anodic dissolution in an electrochemical
cell. The influence of different reaction parameters such as solvent,
electrolyte, voltage–current density, and temperature on the
synthesis yield and textural properties of the MOFs obtained was investigated.
The characterization of the samples involved X-ray diffraction, gas
adsorption, atomic force microscopy, diffuse reflectance infrared
Fourier transform spectroscopy, and scanning electron microscopy.
In the present article, we demonstrate that electrochemical synthesis
is a robust method offering additional degrees of freedom in the synthesis
of these porous materials. The main advantages are the shorter synthesis
time, the milder conditions, the facile synthesis of MOF nanoparticles,
the morphology tuning and the high Faraday efficiencies. The synthesized
MIL-53 and NH2-MIL-53 samples exhibit suppressed framework
flexibility compared to samples synthesized solvothermally.
The NH(2)-MIL-53(Al) metal-organic framework was studied for its use in the separation of CO(2) from CH(4), H(2), N(2)C(2)H(6) and C(3)H(8) mixtures. Isotherms of methane, ethane, propane, hydrogen, nitrogen, and CO(2) were measured. The atypical shape of these isotherms is attributed to the breathing properties of the material, in which a transition from a very narrow pore form to a narrow pore form and from a narrow pore form to a large pore form occurs, depending on the total pressure and the nature of the adsorbate, as demonstrated by in situ XRD patterns measured during adsorption. Apart from CO(2), all tested gases interacted weakly with the adsorbent. As a result, they are excluded from adsorption in the narrow pore form of the material at low pressure. CO(2) interacted much more strongly and was adsorbed in significant amounts at low pressure. This gives the material excellent properties to separate CO(2) from other gases. The separation of CO(2) from methane, nitrogen, hydrogen, or a combination of these gases has been demonstrated by breakthrough experiments using pellets of NH(2)-MIL-53(Al). The effect of total pressure (1-30 bar), gas composition, temperature (303-403 K) and contact time has been examined. In all cases, CO(2) was selectively adsorbed, whereas methane, nitrogen, and hydrogen nearly did not adsorb at all. Regeneration of the adsorbent by thermal treatment, inert purge gas stripping, and pressure swing has been demonstrated. The NH(2)-MIL-53(Al) pellets retained their selectivity and capacity for more than two years.
Small pore size and hydrophobic nature of DD3R make this material a unique zeolite with high potential in industrial separation applications. However, the reproducible rapid synthesis of this zeolite is still a problem. In this work, a thorough assessment of different synthetic methods revealed that synthesis reproducibility relies on two main pillars: the use of properly cleaned autoclave liners and the synthesis composition. High quality DD3R crystals are obtained when KOH is used as a cleaning agent, eliminating memory effects, and when KF is used in the synthesis as a mineralizing agent. H NMR reveals that template molecules accommodated within the cages are sticking to these 8-ring windows through their amine group. High quality DD3R crystals are applied in the adsorptive separation of buta-1,3-diene and but-2-ene isomers, one of the most energy intensive separations in chemical industry. Mixture separation experiments revealed that the 8-ring apertures of the DD3R cages are only accessible to trans-but-2-ene and buta-1,3-diene, while excluding but-1-ene and cis-but-2-ene molecules, resulting in shape-selective separation in the presence of C4 mixtures.
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