English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Preparation of Ni-MCM-41 by equilibrium adsorption — Catalytic evaluation for the direct conversion of ethene to propene

MPS-Authors
/persons/resource/persons86519

Wolff,  T.
Physical and Chemical Foundations of Process Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Max Planck Society;

/persons/resource/persons86525

Zahn,  V. M.
Physical and Chemical Foundations of Process Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Max Planck Society;

/persons/resource/persons86315

Hamel,  C.
Physical and Chemical Foundations of Process Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Max Planck Society;
Otto-von-Guericke-Universität Magdeburg, External Organizations;

/persons/resource/persons86477

Seidel-Morgenstern,  A.
Physical and Chemical Foundations of Process Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Max Planck Society;
Otto-von-Guericke-Universität Magdeburg, External Organizations;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Lehmann, T., Wolff, T., Zahn, V. M., Veit, P., Hamel, C., & Seidel-Morgenstern, A. (2011). Preparation of Ni-MCM-41 by equilibrium adsorption — Catalytic evaluation for the direct conversion of ethene to propene. Catalysis Communications, 12(5), 368-374. doi:10.1016/j.catcom.2010.10.018.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0013-8CC9-3
Abstract
Ni-MCM-41 has been prepared by equilibrium adsorption of different nickel precursors. Nickel citrate and nickel nitrate gave the most active catalysts for the direct transformation of ethene into propene above 250 °C at atmospheric pressure. The maximal ethene conversion at 400 °C was 36% while propene selectivity reached 45%. Analysis of product formation spectra at different temperatures, residence times and inlet compositions revealed reaction kinetics consistent with a sequence of ethene dimerization, positional butene isomerization and propene retro-metathesis. [© 2010 Elsevier B.V. All rights reserved. - accessed February 1st, 2011]