Synthesis of Fe-MCM-41 from silatrane and FeCl3 via sol-gel process and its epoxidation acivity

An iron‐containing mesoporous molecular sieve, or Fe‐MCM‐41, was successfully synthesized the via sol–gel technique using silatrane and FeCl3 as the silicon and iron sources, and was characterized using various techniques. Many factors were investigated, namely, reaction temperature and time, calcin...

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Published inApplied organometallic chemistry Vol. 22; no. 2; pp. 97 - 103
Main Authors Thitsartarn, W., Gulari, E., Wongkasemjit, S.
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.02.2008
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Summary:An iron‐containing mesoporous molecular sieve, or Fe‐MCM‐41, was successfully synthesized the via sol–gel technique using silatrane and FeCl3 as the silicon and iron sources, and was characterized using various techniques. Many factors were investigated, namely, reaction temperature and time, calcination rate, and iron amount in the reaction mixture. It was found that the optimum conditions in which to synthesize Fe‐MCM‐41 was to carry out the reaction at 60 °C for 7 h using a 1 °C min−1 calcination rate and a 550 °C calcination temperature. The catalytic activity and selectivity of styrene epoxidation using hydrogen peroxide showed that the selectivity of the styrene oxide reached 65% at a styrene conversion of 22% over the 1%wt catalyst. Copyright © 2008 John Wiley & Sons, Ltd. Fe‐MCM‐41 was successfully synthesized the via sol–gel technique using silatrane and FeCl3 as the silicon and iron sources. The catalytic activity and selectivity of styrene epoxidation using hydrogen peroxide showed that the selectivity of the styrene oxide reached 65% at a styrene conversion of 22% over the 1%wt catalyst.
Bibliography:ArticleID:AOC1356
Ratchadapisake Sompote Fund
Chulalongkorn University and The Thailand Research Fund
ark:/67375/WNG-Z2GP5QD5-J
istex:AFF235339E61EB92462445B1C9AE2BFEF35A4E01
Postgraduate Education and Research Program in Petroleum and Petrochemical Technology (ADB) Fund
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0268-2605
1099-0739
DOI:10.1002/aoc.1356