Zeolites and metal‐organic frameworks (MOFs) are considered as “competitors” for new separation processes. The production of high‐quality gasoline is currently achieved through the total isomerization process that separates pentane and hexane isomers while not reaching the ultimate goal of a research octane number (RON) higher than 92. This work demonstrates how a synergistic action of the zeolite 5A and the MIL‐160(Al) MOF leads to a novel adsorptive process for octane upgrading of gasoline through an efficient separation of isomers. This innovative mixed‐bed adsorbent strategy encompasses a thermodynamically driven separation of hexane isomers according to the degree of branching by MIL‐160(Al) coupled to a steric rejection of linear isomers by the molecular sieve zeolite 5A. Their adsorptive separation ability is further evaluated under real conditions by sorption breakthrough and continuous cyclic experiments with a mixed bed of shaped adsorbents. Remarkably, at the industrially relevant temperature of 423 K, an ideal sorption hierarchy of low RON over high RON alkanes is achieved, i.e.,
n
‐hexane ≫
n
‐pentane ≫ 2‐methylpentane > 3‐methylpentane ⋙ 2,3‐dimethylbutane > isopentane ≈ 2,2‐dimethylbutane, together with a productivity of 1.14 mol dm
−3
and a high RON of 92, which is a leap‐forward compared with existing processes.
The adsorption equilibrium and kinetics of CO 2 , CH 4 , and N 2 on three types of BETA zeolites were investigated at different temperatures and a defined partial pressure range from dynamic breakthrough experiments. The adsorbed amount followed the decreasing order of CO 2 > CH 4 > N 2 for all studied materials. For the same ratio of SiO 2 /Al 2 O 3 , the Na-BETA-25 zeolite showed a higher uptake capacity than H-BETA-25, due to the presence of a Na + cationic center. Comparing the same H + compensation cation, zeolite H-BETA-25 expressed a slightly higher adsorption capacity than H-BETA-150. Regarding the selectivity of gases, based on their affinity constants, H-BETA-150 displayed the best ability. The adsorption kinetics was considered using the zero-length-column (ZLC) technique. Response surface methodology (RSM) was applied to evaluate the interactions between adsorption parameters and to describe the process.
A series of isoreticular Zr carboxylate MOFs, MIL-140A, B and C, exhibiting 1D microporous triangular shaped channels and based on different aromatic dicarboxylate ligands (1,4-BDC, 2,6-NDC and 4,4’-BPDC, respectively), were...
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