Catalytic properties of Ru-mordenite for NO reduction

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Title: Catalytic properties of Ru-mordenite for NO reduction
Authors: Labhsetwar, Nitin1 nitin_neeri@yahoo.com, Minamino, H.2, Mukherjee, M.1, Mitsuhashi, T.2, Rayalu, S.1, Dhakad, M.1, Haneda, H.2, Subrt, J.3, Devotta, Sukumar1
Source: Journal of Molecular Catalysis A: Chemistry. Jan2007, Vol. 261 Issue 2, p213-217. 5p.
Subjects: Catalysts, Mordenite, Ruthenium, X-ray diffraction
Abstract: Abstract: The reduction of NO by CO over H and Na forms of Ru exchanged mordenite has been studied with ruthenium content of 0.2, 1 and 3wt.%. The catalysts were characterized with respect to X-ray diffraction, BET surface area, temperature programmed oxidation, and temperature programmed desorption of ammonia. These catalysts have been evaluated for their activity for NO–CO reaction using a steady state gas laboratory evaluation assembly. The catalysts show high activity for NO reduction and almost 100% conversion of NO to N2 was observed below 400°C. The activity was found to be a factor of ruthenium content, however, Ru-mordenite in Na form was observed to be relatively more active than Ru-mordenite in H form, probably due to the electron donation from sodium to ruthenium sites. New zeolite phases with improved hydrothermal stability, high surface area and reasonable cation exchange properties can be potential materials for catalytic reduction of NOx. Introduction of active metal ions through ion exchange insures their high dispersion in zeolite supports, which also offer tailoring possibilities for DeNOx catalysts. [Copyright &y& Elsevier]
Copyright of Journal of Molecular Catalysis A: Chemistry is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Catalytic properties of Ru-mordenite for NO reduction
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  Data: <searchLink fieldCode="AR" term="%22Labhsetwar%2C+Nitin%22">Labhsetwar, Nitin</searchLink><relatesTo>1</relatesTo><i> nitin_neeri@yahoo.com</i><br /><searchLink fieldCode="AR" term="%22Minamino%2C+H%2E%22">Minamino, H.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Mukherjee%2C+M%2E%22">Mukherjee, M.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Mitsuhashi%2C+T%2E%22">Mitsuhashi, T.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Rayalu%2C+S%2E%22">Rayalu, S.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Dhakad%2C+M%2E%22">Dhakad, M.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Haneda%2C+H%2E%22">Haneda, H.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Subrt%2C+J%2E%22">Subrt, J.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Devotta%2C+Sukumar%22">Devotta, Sukumar</searchLink><relatesTo>1</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Molecular+Catalysis+A%3A+Chemistry%22">Journal of Molecular Catalysis A: Chemistry</searchLink>. Jan2007, Vol. 261 Issue 2, p213-217. 5p.
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  Data: <searchLink fieldCode="DE" term="%22Catalysts%22">Catalysts</searchLink><br /><searchLink fieldCode="DE" term="%22Mordenite%22">Mordenite</searchLink><br /><searchLink fieldCode="DE" term="%22Ruthenium%22">Ruthenium</searchLink><br /><searchLink fieldCode="DE" term="%22X-ray+diffraction%22">X-ray diffraction</searchLink>
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  Data: Abstract: The reduction of NO by CO over H and Na forms of Ru exchanged mordenite has been studied with ruthenium content of 0.2, 1 and 3wt.%. The catalysts were characterized with respect to X-ray diffraction, BET surface area, temperature programmed oxidation, and temperature programmed desorption of ammonia. These catalysts have been evaluated for their activity for NO–CO reaction using a steady state gas laboratory evaluation assembly. The catalysts show high activity for NO reduction and almost 100% conversion of NO to N2 was observed below 400°C. The activity was found to be a factor of ruthenium content, however, Ru-mordenite in Na form was observed to be relatively more active than Ru-mordenite in H form, probably due to the electron donation from sodium to ruthenium sites. New zeolite phases with improved hydrothermal stability, high surface area and reasonable cation exchange properties can be potential materials for catalytic reduction of NOx. Introduction of active metal ions through ion exchange insures their high dispersion in zeolite supports, which also offer tailoring possibilities for DeNOx catalysts. [Copyright &y& Elsevier]
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  Data: <i>Copyright of Journal of Molecular Catalysis A: Chemistry is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1016/j.molcata.2006.08.013
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        Text: English
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      – SubjectFull: Mordenite
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      – SubjectFull: Ruthenium
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      – SubjectFull: X-ray diffraction
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              Text: Jan2007
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