@article { ISI:000227565800022, title = {Oxidative dehydrogenation of ethylbenzene over vanadia-alumina catalysts in the presence of nitrous oxide: structure-activity relationship}, journal = {Journal of Catalysis}, volume = {230}, number = {2}, year = {2005}, month = {MAR}, pages = {484-492}, publisher = {ACADEMIC PRESS INC ELSEVIER SCIENCE}, type = {Article}, address = {525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA}, abstract = {

A series of vanadia-alumina catalysts with different vanadia contents were prepared by a wet impregnation method. The influence of the local structure of vanadia in these catalysts on the oxidative dehydrogenation of ethylbenzene with nitrous oxide was investigated. The use of N2O as a co-feed remarkably enhanced the styrene yield compared with the use of N-2. Characterization of these vanadia catalysts by XRD, FTIR, UV-vis, TPR, XPS, and V-51 NMR techniques suggests that the nature of the VOx species depends on the vanadia loading: the predominant species are monomeric vanadia at lower loadings, two-dimensional polyvanadates at intermediate loadings, and bulk-like V2O5 and AlVO4 at higher loadings. The rate of oxidative dehydrogenation (ODH) of ethylbenzene per vanadium atom increases with vanadia loading and reaches a maximum at 10 wt\%, the loading at which the surface predominantly contains polyvanadate species. The observed variation in the selectivity of products with vanadium loading indicates that the monomeric V5+ species favors dehydrogenation, whereas bulk-like V2O5 preferentially participates in the dealkylation of ethylbenzene. The vanadium species remains at a higher oxidation state in the presence of N2O, leading to a higher styrene yield. than in a N-2 atmosphere. The ODH turnover rates increased with decreasing energy of the absorption edge in the UV-vis spectrum, at low VOx coverages of less than one monolayer on the Al2O3 surface. (c) 2005 Elsevier Inc. All rights reserved.

}, keywords = {absorption edge energy, Alumina, ethylbenzene, Nitrous oxide, oxidative dehydrogenation, polyvanadates, styrene, vanadia}, issn = {0021-9517}, doi = {10.1016/j.jcat.2005.01.010}, author = {Shiju, N. R. and Anilkumar, Mettu and Mirajkar, Subhash P. and Gopinath, Chinnakonda S. and Rao, B. S. and Satyanarayana, C. V.} } @article { ISI:000240279200017, title = {Vanadium-containing ethane-silica hybrid periodic mesoporous organosilicas: synthesis, structural characterization and catalytic applications}, journal = {Microporous and Mesoporous Materials}, volume = {94}, number = {1-3}, year = {2006}, month = {SEP}, pages = {127-138}, publisher = {ELSEVIER SCIENCE BV}, type = {Article}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

Vanadium-containing ethane-silica hybrid mesoporous silsesquioxane materials (V-HMM) with uniform hexagonal arrangement were prepared using C-18-, C-16- and C-14-alkyl trimethyl ammonium (ATMA) surfactants under basic conditions. The materials were characterized by PXRD, N-2 adsorption-desorption, UV-Visible spectroscopy, Raman, Si-29, C-13 and V-51 solid-state MAS NMR, TEM and SEM techniques. The characterization techniques revealed that the structural ordering, morphology as well as the percentage of metal incorporation depends strongly on the hydrophobic chain length of the surfactant. PXRD, electron microscopy and N-2 adsorptiondesorption analysis confirmed that the original hexagonal structure of the material is maintained after vanadium substitution. UV-Visible, V-51 NMR and Raman analysis certified that vanadium exists in a highly dispersed state and had tetrahedral coordination with the support surface. Liquid-phase epoxidation reaction of styrene using aqueous H2O2 and TBHP as oxidants, showed that the hybrid materials were highly active and more stable than conventional vanadosilicates. The high catalytic activity and improved epoxide selectivity of the V-HMM samples is related to the more hydrophobic environment inside the pore channels than the silica channels in V-MCM-41. (c) 2006 Elsevier Inc. All rights reserved.

}, keywords = {epoxidation, organo vanadosilicates, styrene, V-HMM, V-MCM-41}, issn = {1387-1811}, doi = {10.1016/j.micromeso.2006.03.027}, author = {Shylesh, S. and Singh, A. P.} } @article { ISI:000250026200022, title = {Supported copper oxide as a highly active/selective catalyst for the epoxidation of styrene by TBHP to styrene oxide}, journal = {Catalysis Communications}, volume = {8}, number = {10}, year = {2007}, month = {OCT}, pages = {1556-1560}, publisher = {ELSEVIER SCIENCE BV}, type = {Article}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

Liquid phase epoxidation of styrene by anhydrous and aqueous TBHP to styrene oxide has been studied under reflux, using different supported CuO (viz. Cuo/Si-MCM-41, CuO/Al2O3, CuO/Ga2O3 and CuO/In2O3) as easily separable and reusable heterogeneous catalysts. The CuO/Ga2O3 catalyst showed the best performance in the epoxidation by aqueous TBHP. The CuO supported on In2O3 or Si-MCM-41 also showed very good performance in the epoxidation but only by anhydrous TBHP. However, the CUO/SiO2 catalyst, however, showed very good performance in the epoxidation by both the anhydrous and aqueous TBHP. Influence of the reaction conditions (temperature, time and TBHP/styrene ratio) on the epoxidation by aqueous TBHP over the best catalyst (CuO/Ga2O3) has been investigated. (C) 2007 Elsevier B.V. All rights reserved.

}, keywords = {CuO/Al2O3, CuO/Ga2O3, CuO/In2O3, Cuo/Si-MCM-41, CuO/SiO2, epoxidation, styrene, Styrene oxide, tertiary butyl hydroperoxide}, issn = {1566-7367}, doi = {10.1016/j.catcom.2007.01.005}, author = {Choudhary, Vasant R. and Jha, Rani and Chaudhari, Nitin K. and Jana, Prabhas} } @article { ISI:000260988200019, title = {Selective epoxidation of styrene to styrene oxide by TBHP using simple transition metal oxides (NiO, CoO or MoO3) as highly active environmentally-friendly catalyst}, journal = {Catalysis Communications}, volume = {10}, number = {2}, year = {2008}, month = {NOV}, pages = {205-207}, publisher = {ELSEVIER SCIENCE BV}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

Simple transition metal oxides, such as NiO, CoO or MoO3, etc. show high catalytic activity for the selective epoxidation of styrene to styrene oxide by TBHP. The order of choice for different transition metal oxides for epoxidation is NiO \> CoO \> MoO3 \> Cr2O3 \> Fe2O3 \> ZnO \>= U3O8 \>\> TiO2 \>\> MnO2. (C) 2008 Elsevier B.V. All rights reserved.

}, keywords = {CoO, epoxidation, MoO3, NiO, styrene, Styrene oxide, TBHP}, issn = {1566-7367}, doi = {10.1016/j.catcom.2008.08.020}, author = {Choudhary, Vasant R. and Jha, Rani and Jana, Prabhas} } @article { ISI:000269259100007, title = {Supported nano-gold catalysts for epoxidation of styrene and oxidation of benzyl alcohol to benzaldehyde}, journal = {Topics in Catalysis}, volume = {52}, number = {12}, year = {2009}, month = {NOV}, pages = {1677-1687}, publisher = {SPRINGER/PLENUM PUBLISHERS}, address = {233 SPRING ST, NEW YORK, NY 10013 USA}, abstract = {

Nano-gold particles supported on different alkaline earth oxides (viz. MgO, CaO, BaO and SrO), Gr. IIIa metal oxides (viz. Al(2)O(3), Ga(2)O(3), In(2)O(3) and Tl(2)O(3)), transition metal oxides (viz. TiO(2), Cr(2)O(3), MnO(2), Fe(2)O(3), CoO(x), NiO, CuO, ZnO, Y(2)O(3) and ZrO(2)), rare earth metal oxides (viz. La(2)O(3), Ce(2)O(3), Nd(2)O(3), Sm(2)O(3), Eu(2)O(3), Tb(2)O(3), Er(2)O(3) and Yb(2)O(3)) and U(3)O(8) [all prepared by depositing gold on corresponding metal oxide support by deposition precipitation (DP) and/or homogeneous deposition precipitation (HDP) method] were evaluated for their catalytic performance in the liquid phase epoxidation of styrene by tert-butyl hydroperoxide (TBHP) to styrene oxide and also in the solvent-free benzyl alcohol-to-benzaldehyde oxidation (by molecular oxygen or TBHP) reactions. For the epoxidation, the catalytic performance (styrene oxide yield) of the most promising nano-gold catalysts prepared by the HDP method was in the following order: Au/MgO \> Au/Tl(2)O(3) \> Au/Yb(2)O(3) \> Au/Tb(2)O(3) \> Au/CaO (or TiO(2)). However, for the oxidation of benzyl alcohol to benzaldehyde by molecular oxygen, the order of choice for the most promising catalysts (based on benzaldehyde yield) was Au/U(3)O(8) \> Au/Al(2)O(3) \> Au/ZrO(2) \> Au/MgO. Whereas, when TBHP was used as an oxidizing agent for the benzyl alcohol oxidation, the order of choice for the most promising catalysts was Au/U(3)O(8) \> Au/MgO \> Au/TiO(2) \> Au/ZrO(2) \> Au/Al(2)O(3). The catalytic performance of a particular supported nano-gold catalyst was thus found to depend on the reaction catalysed by them. Moreover, it is strongly influenced by a number of catalyst parameters, such as the metal oxide support, the method of gold depositon on the support, the gold loading and also on the catalyst calcination temperature. Nano-gold particles-support interactions seem to play an important role in controlling the deposition of gold ( amount of gold deposited and size and morphology of gold particles), formation of different surface gold species (Au(0), Au(1+) and Au(3+)) and electronic properties of gold particles and, consequently, control the catalytic performance (both the activity and selectivity) of the supported nano-gold catalysts in the reactions. The nano-gold catalysts prepared by the HDP method showed much better catalytic performance than those prepared by the DP, coprecipitation or impregnation method; in general, the HDP method provided supported gold catalysts with much higher gold loading and/or smaller size gold particles than that achieved by the DP and other methods.

}, keywords = {Benzaldehyde, Benzyl alcohol, epoxidation, Metal oxide supports, Nano-gold catalysts, Oxidation, styrene, Styrene oxide}, issn = {1022-5528}, doi = {10.1007/s11244-009-9306-1}, author = {Choudhary, Vasant R. and Dumbre, Deepa K.} } @article { ISI:000288434800016, title = {Kinetics studies and mechanism evolution of the epoxidation of styrene over nanoporous Au doped TS-1}, journal = {Polish Journal of Chemical Technology}, volume = {12}, number = {4}, year = {2010}, month = {JAN}, pages = {72-78}, publisher = {VERSITA}, address = {SOLIPSKA 14A-1, 02-482 WARSAW, POLAND}, abstract = {

{A kinetic investigation of the slurry phase epoxidation of styrene with hydrogen peroxide has been carried out, for the first time, over nanoporous Au doped TS-1 catalyst, in a batch reactor, in the temperature range of 313-333 K. It was found that product selectivity and the rate of reaction are greatly influenced by concentrations of styrene and hydrogen peroxide. Kinetics studies reveal that the mechanism of the reaction is of the {\textquoteleft}{\textquoteleft}Redox{\textquoteright}{\textquoteright} type. The rate equation

}, keywords = {Au/TS-1, epoxidation, kinetics, styrene, Styrene oxide}, issn = {1509-8117}, doi = {10.2478/v10026-010-0054-6}, author = {Saxena, Samidha and Dwivedi, Reena and Bhadauria, Sheenu and Chumbhale, Vilas R. and Prasad, Rajendra} }