Reconstructed Mg-Al hydrotalcites prepared by using different rehydration and drying time: Physico-chemical properties and catalytic performance in aldol condensation
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22320%2F17%3A43913297" target="_blank" >RIV/60461373:22320/17:43913297 - isvavai.cz</a>
Alternative codes found
RIV/62243136:_____/17:N0000003 RIV/60461373:22350/17:43913297
Result on the web
<a href="http://www.sciencedirect.com.ezproxy.vscht.cz/science/article/pii/S0926860X17300856?via%3Dihub" target="_blank" >http://www.sciencedirect.com.ezproxy.vscht.cz/science/article/pii/S0926860X17300856?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.apcata.2017.02.020" target="_blank" >10.1016/j.apcata.2017.02.020</a>
Alternative languages
Result language
angličtina
Original language name
Reconstructed Mg-Al hydrotalcites prepared by using different rehydration and drying time: Physico-chemical properties and catalytic performance in aldol condensation
Original language description
Aldol condensation in presence of reconstructed hydrotalcites as basic catalysts is well documented and attracts an increased attention because it allows producing complex molecules starting from relatively simpler ones. Nevertheless, more studies are necessary for the better understanding of preparation factors that affect the physico-chemical properties of these materials and their catalytic performance. This work considers the effect of the duration of the liquid-phase rehydration of Mg-Al mixed oxide as well as the drying duration of prepared samples on their physico-chemical properties and performance in aldol condensation of furfural and acetone. The properties of all materials were investigated by XRD, TGA, TGA-MS, SEM and DRIFT. Experiments on aldol condensation of furfural and acetone were performed by using a stirred batch reactor at T = 25 °C with Ac:F = 5 molar ratio. The characterization of the prepared materials showed that the recovery of HTC structure occurred within a few seconds of the contact between Mg-Al mixed oxide with liquid water. The content of functional species in all reconstituted HTCs was nearly constant and independent on preparation conditions while the amount of physisorbed water in the prepared samples decreased with increasing drying time. The calcination of as-prepared HTC followed by the subsequent rehydration of Mg-Al mixed oxide resulted in the replacement of >90% carbonate groups on hydroxyls which are Br?nsted basic sites. Consequently, the activity of the reconstructed HTCs in aldol condensation of furfural and acetone was significantly higher compared to Mg-Al mixed oxide. The catalytic performance of rehydrated materials was almost independent on rehydration time while furfural conversion decreased if carrying out the reaction in an aqueous medium with increased water content. On the other hand, properly dried reconstructed HTC with the absence of physisorbed water also exhibited a very low activity in the reaction.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10403 - Physical chemistry
Result continuities
Project
<a href="/en/project/GA15-21817S" target="_blank" >GA15-21817S: Analysis of the structure/activity relationship of Mg/Al, Ca/Al and Zn/Al mixed oxides in aldol condensation and transesterification reactions</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
APPLIED CATALYSIS A-GENERAL
ISSN
0926-860X
e-ISSN
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Volume of the periodical
536
Issue of the periodical within the volume
APR 25 2017
Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
12
Pages from-to
85-96
UT code for WoS article
000398647200010
EID of the result in the Scopus database
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