High surface area vanadium phosphate catalysts for n-butane oxidation

Vanadium phosphorus oxide (VPO) was prepared using the precipitation procedure and tested for potential use in the partial oxidation reaction of n-butane to maleic anhydride. In particular, the effect of reducing agents such as the isobutanol, 1-butanol, and glycol, subsequent water treatment, and m...

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Main Authors: Rownaghi, Ali Asghar, Yap, Taufiq Yun Hin, Rezaei, Fateme
Format: Article
Language:English
Published: American Chemical Society 2009
Online Access:http://psasir.upm.edu.my/id/eprint/15006/1/High%20surface%20area%20vanadium%20phosphate%20catalysts%20for%20n.pdf
http://psasir.upm.edu.my/id/eprint/15006/
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spelling my.upm.eprints.150062016-11-29T08:10:51Z http://psasir.upm.edu.my/id/eprint/15006/ High surface area vanadium phosphate catalysts for n-butane oxidation Rownaghi, Ali Asghar Yap, Taufiq Yun Hin Rezaei, Fateme Vanadium phosphorus oxide (VPO) was prepared using the precipitation procedure and tested for potential use in the partial oxidation reaction of n-butane to maleic anhydride. In particular, the effect of reducing agents such as the isobutanol, 1-butanol, and glycol, subsequent water treatment, and microwave heating were investigated in detail. The optimum synthesis conditions were identified with respect to catalyst activity for the oxidation of n-butane. The activity and selectivity of VPO prepared catalysts have been evaluated in a fixed bed microreactor and in situ gas chromatography (GC) was used to evaluate the system efficiency and analyze the product effluent stream. The different catalysts exhibited a range of activities and selectivities under the same reaction conditions. The range in catalyst performance may be attributed to the crystal size as well as particle size of catalyst. The results were interpreted in terms of surface area and catalyst nanostructure, and it has been generally concluded that the catalyst surface area is enhanced by the employment of glycol as the reducing agent, followed refluxing by distilled water and drying by microwave irradiation. The catalyst produced using this method is the most active and selective catalyst for partial oxidation of n-butane to maleic anhydride. The catalyst lifetime was tested under the optimum reaction conditions, and the catalyst was found to be highly stable for more than 70 h. The characterization of both precursors and calcined catalysts was carried out using X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectrometer (ICP-AES), Brunauer−Emmer−Teller (BET) surface area measurement, temperature programmed reduction (H2-TPR), and scanning electron microscopy (SEM). American Chemical Society 2009 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/15006/1/High%20surface%20area%20vanadium%20phosphate%20catalysts%20for%20n.pdf Rownaghi, Ali Asghar and Yap, Taufiq Yun Hin and Rezaei, Fateme (2009) High surface area vanadium phosphate catalysts for n-butane oxidation. Industrial & Engineering Chemistry Research, 48 (16). pp. 7517-7528. ISSN 0888-5885; ESSN: 1520-5045 10.1021/ie900238a
institution Universiti Putra Malaysia
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collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
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language English
description Vanadium phosphorus oxide (VPO) was prepared using the precipitation procedure and tested for potential use in the partial oxidation reaction of n-butane to maleic anhydride. In particular, the effect of reducing agents such as the isobutanol, 1-butanol, and glycol, subsequent water treatment, and microwave heating were investigated in detail. The optimum synthesis conditions were identified with respect to catalyst activity for the oxidation of n-butane. The activity and selectivity of VPO prepared catalysts have been evaluated in a fixed bed microreactor and in situ gas chromatography (GC) was used to evaluate the system efficiency and analyze the product effluent stream. The different catalysts exhibited a range of activities and selectivities under the same reaction conditions. The range in catalyst performance may be attributed to the crystal size as well as particle size of catalyst. The results were interpreted in terms of surface area and catalyst nanostructure, and it has been generally concluded that the catalyst surface area is enhanced by the employment of glycol as the reducing agent, followed refluxing by distilled water and drying by microwave irradiation. The catalyst produced using this method is the most active and selective catalyst for partial oxidation of n-butane to maleic anhydride. The catalyst lifetime was tested under the optimum reaction conditions, and the catalyst was found to be highly stable for more than 70 h. The characterization of both precursors and calcined catalysts was carried out using X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectrometer (ICP-AES), Brunauer−Emmer−Teller (BET) surface area measurement, temperature programmed reduction (H2-TPR), and scanning electron microscopy (SEM).
format Article
author Rownaghi, Ali Asghar
Yap, Taufiq Yun Hin
Rezaei, Fateme
spellingShingle Rownaghi, Ali Asghar
Yap, Taufiq Yun Hin
Rezaei, Fateme
High surface area vanadium phosphate catalysts for n-butane oxidation
author_facet Rownaghi, Ali Asghar
Yap, Taufiq Yun Hin
Rezaei, Fateme
author_sort Rownaghi, Ali Asghar
title High surface area vanadium phosphate catalysts for n-butane oxidation
title_short High surface area vanadium phosphate catalysts for n-butane oxidation
title_full High surface area vanadium phosphate catalysts for n-butane oxidation
title_fullStr High surface area vanadium phosphate catalysts for n-butane oxidation
title_full_unstemmed High surface area vanadium phosphate catalysts for n-butane oxidation
title_sort high surface area vanadium phosphate catalysts for n-butane oxidation
publisher American Chemical Society
publishDate 2009
url http://psasir.upm.edu.my/id/eprint/15006/1/High%20surface%20area%20vanadium%20phosphate%20catalysts%20for%20n.pdf
http://psasir.upm.edu.my/id/eprint/15006/
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