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• W2000795528 abstract "The effect of the support for rhodium on activated carbon, and the effect of precursor for cobalt on silica, were studied in the liquid phase hydroformylation of 1-hexene. At best the activities of the heterogeneous catalysts were similar to their homogeneous counterparts. The activity of the RhC catalysts correlated with the support; the larger the pores the better the mass transfer, and the higher the activity. In the case of CoSiO2, the effect of precursor on the activity of the catalysts was diverse, and the activities remained lower than that of the homogeneous cobalt carbonyl. Some metal was, however, dissolved from the supports, and consequently the activity was mainly due to the dissolved catalytic species rather than the heterogeneous catalyst. The dissolution of the metal from the support was due to both synthesis gas mediated formation of soluble active species, and reaction product effectuated dissolution. Yet, the heterogeneous functionality of the active carbon support was revealed by the formation of C21 acetals, which were formed on a support with acidic character and large enough pores. The acidic character of the active carbon supports was also shown by the formation of C14 condensation products, which were only formed in traces for homogeneous rhodium." @default.
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• W2000795528 date "1997-07-01" @default.
• W2000795528 modified "2023-10-12" @default.
• W2000795528 title "Hydroformylation of 1-hexene on RhC and CoSiO2 catalysts" @default.
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• W2000795528 doi "https://doi.org/10.1016/s1381-1169(96)00461-x" @default.
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