화학공학소재연구정보센터
Journal of Molecular Catalysis A-Chemical, Vol.248, No.1-2, 10-16, 2006
On the kinetics of iridium nanoparticles formation in ionic liquids and olefin hydrogenation
The in situ formation of an iridium nanoparticles dispersion obtained from the reduction of the organometallic precursor [Ir(cod)CI](2) in I-n-butyl-3-methyl imidazolium hexafluorophosphate ionic liquid by molecular hydrogen is an autocatalytic process. These nanoparticles possess a small size and a monomodal size distribution of 2.0 +/- 0.4 nm iridium nanoparticles can be confirmed by TEM and XRD analysis before and after the catalytic process. The I-decene hydrogenation by the Ir(0) nanoparticles in the ionic liquid follows the classical monomolecular surface reaction mechanism (v = kc K[S]/I+K[S]). The reaction rate is a mass controlled process under hydrogen pressure < 4 atm. The catalytic kinetic constant (k(c)) and the adsorption constant (K) under hydrogen pressures >= 4 atm are independent of the hydrogen concentration indicating zero order dependence on hydrogen pressure and the reaction depends only of the I-decene concentration in the ionic liquid. (c) 2005 Elsevier B.V. All rights reserved.