HYDROGENATIONOF ACETYLENE COMPOUNDS ON MULTICOMPONENT RANEY NICKEL (SKELETON CATALYST)

Authors

  • Zh. K. Kairbekov Non-commercial joint-stock company “Al-Farabi Kazakh National university”
  • I. М. Jeldybayeva Non-commercial joint-stock company “Al-Farabi Kazakh National university”
  • S.M. Suimbayeva Non-commercial joint-stock company “Al-Farabi Kazakh National university”
  • SH. Non-commercial joint-stock company “Al-Farabi Kazakh National university”

Keywords:

acetylene compounds, phenylacetylene, hexine, hexane, hydrogenation, Raney nickel, catalytic “bedpan”, modifying additives, activity, selectivity

Abstract

This work presents the results of a study of the catalytic activity and selectivity of multicomponent Raney nickel in the hydrogenation of phenylacetylene and hexine2.Hexin-2 is hydrogenated on Raney nickel selectively and stereospecifically, with the formation of mainly cis-hexene-2. The activity, selectivity and isomerizing ability of modified Raney nickel obtained from Ni-Al-Me and Ni-Al-Me1 -Me2 alloys (where Me-Cu, Ag, Zn, Ti, Zr, Sn, Pb, Ta, Bi, Cr, Mo, Mn, Fe, and Pd) in the reactions of hydrogenation of phenylacetylene, hexin-2 substantially depend on the nature of the additives introduced into the Ni-Al alloy.In hexin-2 hydrogenation reactions, multicomponent Raney nickel exhibit high stereociphicity. The yield ratio of cis-hexene-2 / trans-hexene-2 is 16-25, depending on the nature of the modifying additive.

References

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Published

2021-05-03