کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
50524 | 46800 | 2011 | 7 صفحه PDF | دانلود رایگان |
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.
Figure optionsDownload as PowerPoint slideResearch Highlights
► Equilibrium adsorption gave active catalysts for the ethene to propene reaction.
► Maximal propene selectivity was 45% combined with an ethene conversion of 36%.
► Only minor amounts of byproducts (ethane, iso-butene, and hexenes) were formed.
► Reaction network: ethene dimerization, butene isomerization, and propene retro-metathesis.
► Moderate catalyst deactivation at 375 °C: conversion drop from 36 to 25% in 55 h.
Journal: Catalysis Communications - Volume 12, Issue 5, 5 January 2011, Pages 368–374