Document details

A microporous multi‐cage metal–organic framework for an effective one‐step separation of branched alkanes feeds

Author(s): Zhou, Lin ; Brântuas, Pedro ; Henrique, Adriano ; Reinsch, Helge ; Wahiduzzaman, Mohammad ; Grenèche, Jean‐Marc ; Rodrigues, Alírio ; Silva, José A.C. ; Maurin, Guillaume ; Serre, Christian

Date: 2024

Persistent ID: http://hdl.handle.net/10198/29765

Origin: Biblioteca Digital do IPB

Subject(s): Ultra-microporous metal-organic framework; Isoreticular chemistry; Pentane and hexane alkane isomers separation; Octane upgrading of gasoline


Description

The improvement of the Total Isomerization Process (TIP) for the production of high-quality gasoline with the ultimate goal of reaching a Research Octane Number (RON) higher than 92 requires the use of specific sorbents to separate pentane and hexane isomers into classes of linear, mono- and di-branched isomers. Herein we report the design of a new multi-cage microporous Fe(III)-MOF (referred to as MIP-214, MIP stands for materials of the Institute of Porous Materials of Paris) with a flu-e topology, incorporating an asymmetric heterofunctional ditopic ligand, 4-pyrazolecarboxylic acid, that exhibits an appropriate microporous structure for a thermodynamic-controlled separation of hydrocarbon isomers. This MOF produced via a direct, scalable, and mild synthesis route was proven to encompass a unique separation of C5/C6 isomers by classes of low RON over high RON alkanes with a sorption hierarchy: (n-hexane >> n-pentane approximate to 2-methylpentane>3-methylpentane)(low RON)>>(2,3-dimethylbutane approximate to i-pentane approximate to 2,2-dimethylbutane)(high RON) following the adsorption enthalpy sequence. We reveal for the first time that a single sorbent can efficiently separate such a complex mixture of high RON di-branched hexane and mono-branched pentane isomers from their low RON counterparts, which is a major achievement reported so far.

Document Type Journal article
Language English
Contributor(s) Biblioteca Digital do IPB
CC Licence
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