In Situ Vibrational Spectroscopic Investigation of C4 Hydrocarbon Selective Oxidation Over Vanadium-phosphorus-oxide Catalysts


Book Description

N-Butane selective oxidation over the VPO catalyst to maleic anhydride is the first and only commercialized process of light alkane selective oxidation. The mechanism of this reaction is still not well known despite over twenty years of extensive studies, which can partially be attributed to the extreme difficulties to characterize catalytic reactions real-time under typical reaction conditions. In situ spectroscopic characterization techniques such as Infrared spectroscopy and laser Raman spectroscopy were used in the current mechanistic investigations of n-butane oxidation over VPO catalysts. To identify the reaction intermediates, oxidation of n-butane, 1,3-butadiene and related oxygenates on the VPO catalyst were monitored using FTIR spectroscopy under transient conditions. n-Butane was found to adsorb on the VPO catalyst to form olefinic species, which were further oxidized to unsaturated, noncyclic carbonyl species. The open chain dicarbonyl species then experienced cycloaddition to form maleic anhydride. VPO catalyst phase transformations were investigated using in situ laser Raman spectroscopy. This report contains Chapter 1: General introduction; Chapter 2: Literature review; and Chapter 5: Conclusion and recommendations.




In Situ Vibrational Spectroscopic Investigation of C{sub 4} Hydrocarbon Selective Oxidation Over Vanadium-phosphorus-oxide Catalysts


Book Description

N-Butane selective oxidation over the VPO catalyst to maleic anhydride is the first and only commercialized process of light alkane selective oxidation. The mechanism of this reaction is still not well known despite over twenty years of extensive studies, which can partially be attributed to the extreme difficulties to characterize catalytic reactions real-time under typical reaction conditions. In situ spectroscopic characterization techniques such as Infrared spectroscopy and laser Raman spectroscopy were used in the current mechanistic investigations of n-butane oxidation over VPO catalysts. To identify the reaction intermediates, oxidation of n-butane, 1,3-butadiene and related oxygenates on the VPO catalyst were monitored using FTIR spectroscopy under transient conditions. n-Butane was found to adsorb on the VPO catalyst to form olefinic species, which were further oxidized to unsaturated, noncyclic carbonyl species. The open chain dicarbonyl species then experienced cycloaddition to form maleic anhydride. VPO catalyst phase transformations were investigated using in situ laser Raman spectroscopy. This report contains Chapter 1: General introduction; Chapter 2: Literature review; and Chapter 5: Conclusion and recommendations.







Preparation and Characterisation of Vanadium Phosphorus Oxide Catalysts for Butane Oxidation to Maleic Anhydride


Book Description

This thesis aims the study of new preparative routes to get catalyst precursors VOHPO4.0.5H2O with good catalytic performance for the selective oxidation of n-butane to maleic anhydride. The use of octane as co-solvent shows a significant effect on the morphology of VOHPO4.0.5H2O precursor which was prepared via three different routes. The reaction of VOPO4.2H2O with octane solvent shows the possibility of the intercalation of the octane solvent between the layers of VOPO4.2H2O. This can lead to the formation of VOHPO4.0.5H2O precursors with a new morphology after the reduction step using 1-butanol. In addition, the use of octane as co-solvent with 1-butanol leads to the formation of VOHPO4.0.5H 2O with a different XRD pattern and new morphology. Testing these samples shows that the samples with rosette morphology exhibit the highest conversion and selectivity compared with the new materials prepared. We demonstrate that the use of seed crystals of vanadium phosphate can have a dramatic influence on the morphology and phase identity of the precursor materials. VOHPO4.0.5H2O was prepared from VOPO 4.2H2O using 1- and 3-octanol, 2-butanol and 2-methyl-1-propanol as both solvent and reducing agent. With 1-octanol the reaction temperature was found to be crucial in obtaining a high yield of the precursor phase, and at temperatures ≥160°C a solution, containing V4+ ions formed in preference to VOHPO4.0.5H2O. However, VOHPO4.0.5H2O formation can be achieved by the addition of a small amount of V-P-O materials as seeds if carrying out the reduction process above this temperature. In contrast, when 3-octanol is used, VO(H 2PO4)2 is formed solely, but in the presence of a V-P-O seed significant amounts of VOHPO4.0.5H2O can also be formed. Studying the reaction time online shows that VO(H2PO 4)2 could be transformed to VOHPO4.0.5H2 O, which has been attempted previously without success. Finally, testing these samples under reaction conditions shows that they demonstrate high selectivity toward MA and good conversion compared to VO(H2PO4) 2. Vanadium phosphate catalysts have successfully been prepared in aqueous media using hydrogen. The catalysts precursors obtained were poorly crystalline VOHPO4.05H2O and a minor amount of an impurity detected by a reflection in the XRD pattern. Activating these materials for n-butane oxidation show low selectivity of MA (5%), which could be attributed to the presence of V(V) phases after activation.




Elementary Reaction Steps in Heterogeneous Catalysis


Book Description

This book comprises the proceedings of a NATO sponsored Advanced Research Workshop held from 1st November to 6th November 1992 in the delightful Chateau de Florans, Bedoin, Vaucluse, France and entitled 'Elementary Reaction Steps in Heterogeneous Catalysis. ' The organisers are grateful to the Science Committee of NATO for their support of this meeting. This is believed to be the first wide ranging NATO ARW in the field of heterogeneous catalysis for 20 years, following a previous venture organised in Sardinia by Basolo and Burwell, of Northwestern University, Illinois, USA [1]. This volume collects the lecture presentations and reports on the lively Panel discussions. The idea for the meeting evolved from a series of International Symposia on Quantum Chemistry and Mechanism in Heterogeneous Catalysis. The first of these was held in Lyon, France in 1986, the second in Krakow, Poland in 1988 and the third in Berkeley, California in 1990. The organising committee of the present meeting was Bernard Bigot, France, Tony Farragher, Netherlands, Richard Joyner, UK, Mme. Danielle Olivier, France, and Rutger van Santen, Netherlands, (Chairman). We wish to thank all members of the committee but in particular Bernard Bigot, who undertook the very extensive work involved in the local organisation with consummate skill and made our stay in Provence a great pleasure. Bernard Bigot's secretary, Mme. Marie-Noelle Coscat and Richard Joyner's secretary, Mrs. Pat Gibbs, also deserve our considerable thanks. There were fifty-four participants from eleven countries.