Surface organometallic chemistry on metals in water - Chemical modification of platinum catalyst surface by reaction with hydrosoluble organotin complexes: application to the selective dehydrogenation of isobutane to isobutene

Surface organo-metallic chemistry on metals can be a new route to generate supported bimetallic catalysts. According to previous works on Pt-Sn cataly sts, the reaction of tetra n-butyl-tin on the reduced platinum surface lead s to well-defined bimetallic catalysts which are very active and selective in the dehydrogenation of isobutane into isobutene. The presence of tin not only isolates the surface platinum atoms from each other (EXAFS) and thus prevents a fast deactivation by decreasing the processes of C-C bond cleava ge but also favors the regeneration processes under air. So far the catalys t preparations were carried out either in the gas phase or in organic solut ion (e.g. heptane). However, in order to meet the industrial criteria of pr ocess simplicity, there is a need to carry out such catalyst preparation in water. In this work, Pt-Sn/Al2O3 and Pt-Sn/SiO2 catalysts was prepared by reacting tris n-butyl-tin hydroxide on the platinum surface, in water solution unde r atmospheric pressure of hydrogen. The kinetics of the reaction was follow ed by measuring the amount of butane evolved as a function of time. The sol ids obtained were characterized by CO, O-2 or H-2 chemisorption and electro n microscopy (CTEM and EDAX). Clearly, the (n-Bu)(3)Sn(OH) reacts selective ly on the platinum surface and not with the support, with evolution of buta ne, leading to a bimetallic catalyst where the platinum atoms are isolated from each other by the tin atoms. Very high selectivities (> 95%) and activ ities were obtained for the reaction of isobutane dehydrogenation into isob utene and it was concluded that surface organo-metallic chemistry on metal in water can be an alternative route to prepare well-defined supported bime tallic Pt-Sn catalysts. (C) 2001 Elsevier Science B.V. All rights reserved.