“…In contrast, at 40 C, yields were approximately equal; these equilibrium yields are easily achieved at high temperatures due to high reaction rates (kinetic limitation). Ibragimov et al 46 observed similar results for the isomerization of n-hexane in 1-methyl-3-butylimidazolium chloride with AlCl 3 .…”
“…In contrast, at 40 C, yields were approximately equal; these equilibrium yields are easily achieved at high temperatures due to high reaction rates (kinetic limitation). Ibragimov et al 46 observed similar results for the isomerization of n-hexane in 1-methyl-3-butylimidazolium chloride with AlCl 3 .…”
“…After isomerization, nalkanes that have not been converted to branched alkanes are returned to the reactor. [1][2][3] Therefore, a mixture of branched and linear alkanes has to be separated. For light hydrocarbons, the typical boiling points of their isomers are relatively close which makes basic separation methods like cryo-distillation extremely energy consuming.…”
Kinetic and thermodynamic separation of n-pentane and isopentane isomers by a dehydroxylated UiO-66 (Zr) metal–organic framework is explored using 2H NMR coupled with molecular dynamics (MD, GCMC MD) simulations.
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