dc.contributor.author |
Kesavan Pillai, Sreejarani
|
|
dc.contributor.author |
Gheevarghese, O
|
|
dc.contributor.author |
Tleane, IV
|
|
dc.date.accessioned |
2013-04-19T06:30:46Z |
|
dc.date.available |
2013-04-19T06:30:46Z |
|
dc.date.issued |
2012 |
|
dc.identifier.citation |
Kesavan Pillai, S., Gheevarghese, O. and Tleane, I.V. 2012. Friedel-Crafts Alkylation of o-xylene over V2O5/ZrO2 Catalysts. Mapana Journal of Sciences, vol. 11(2), pp 1-16 |
en_US |
dc.identifier.issn |
0975-3303 |
|
dc.identifier.uri |
http://journals.christuniversity.in/index.php/mapana/article/view/259
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|
dc.identifier.uri |
http://hdl.handle.net/10204/6703
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|
dc.description |
Copyright: 2012 Mapana Journal of Sciences, vol. 11(2), pp 1-16 |
en_US |
dc.description.abstract |
The present study has undertaken the Friedel-Crafts benzylation of aromatics over the V2O5/ZrO2 catalysts systems. Catalysts with different V2O5 content (0-15wt %) was prepared by wet impregnation method and characterized by XRD, BET surface area, FTIR and 5’V NMR techniques. The surface acidic properties were determined by temperature programmed desorption of NH3, cumene cracking and perylene adsorption. Under the optimized reaction conditions, these catalysts are found to be very effective and considerably more selective than the conventional homogeneous Lewis acid catalysts. The investigation of vanadia systems-catalyzed benzylation of o-xylene with benzyl chloride revealed that the catalytic activity and product selectivity are sensitive to the precise reaction parameters and can be related to the Lewis acidity of the systems. The reaction is found to be very clean and produces the desired monoalkylated product with high yield. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Mapana Journal of Sciences |
en_US |
dc.relation.ispartofseries |
Workflow;10364 |
|
dc.subject |
V2O5/ZrO2 catalysts |
en_US |
dc.subject |
Friedel-Crafts alkylation |
en_US |
dc.subject |
Lewis acidity |
en_US |
dc.title |
Friedel-Crafts Alkylation of o-xylene over V2O5/ZrO2 Catalysts |
en_US |
dc.type |
Article |
en_US |
dc.identifier.apacitation |
Kesavan Pillai, S., Gheevarghese, O., & Tleane, I. (2012). Friedel-Crafts Alkylation of o-xylene over V2O5/ZrO2 Catalysts. http://hdl.handle.net/10204/6703 |
en_ZA |
dc.identifier.chicagocitation |
Kesavan Pillai, Sreejarani, O Gheevarghese, and IV Tleane "Friedel-Crafts Alkylation of o-xylene over V2O5/ZrO2 Catalysts." (2012) http://hdl.handle.net/10204/6703 |
en_ZA |
dc.identifier.vancouvercitation |
Kesavan Pillai S, Gheevarghese O, Tleane I. Friedel-Crafts Alkylation of o-xylene over V2O5/ZrO2 Catalysts. 2012; http://hdl.handle.net/10204/6703. |
en_ZA |
dc.identifier.ris |
TY - Article
AU - Kesavan Pillai, Sreejarani
AU - Gheevarghese, O
AU - Tleane, IV
AB - The present study has undertaken the Friedel-Crafts benzylation of aromatics over the V2O5/ZrO2 catalysts systems. Catalysts with different V2O5 content (0-15wt %) was prepared by wet impregnation method and characterized by XRD, BET surface area, FTIR and 5’V NMR techniques. The surface acidic properties were determined by temperature programmed desorption of NH3, cumene cracking and perylene adsorption. Under the optimized reaction conditions, these catalysts are found to be very effective and considerably more selective than the conventional homogeneous Lewis acid catalysts. The investigation of vanadia systems-catalyzed benzylation of o-xylene with benzyl chloride revealed that the catalytic activity and product selectivity are sensitive to the precise reaction parameters and can be related to the Lewis acidity of the systems. The reaction is found to be very clean and produces the desired monoalkylated product with high yield.
DA - 2012
DB - ResearchSpace
DP - CSIR
KW - V2O5/ZrO2 catalysts
KW - Friedel-Crafts alkylation
KW - Lewis acidity
LK - https://researchspace.csir.co.za
PY - 2012
SM - 0975-3303
T1 - Friedel-Crafts Alkylation of o-xylene over V2O5/ZrO2 Catalysts
TI - Friedel-Crafts Alkylation of o-xylene over V2O5/ZrO2 Catalysts
UR - http://hdl.handle.net/10204/6703
ER -
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en_ZA |