Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst

The interaction of molecular hydrogen with the surface of MoO3–ZrO2 was observed using infrared IR and electron spin resonance (ESR) spectroscopy, and the hydrogen adsorption was quantitatively evaluated in the temperature range of 323–573 K. The hydrogen adsorbed IR results confirmed the formation...

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Main Authors: Ruslan, Nurun Najwa, Triwahyono, Sugeng, Abdul Jalil, Aishah, Timmiati, Sharifah Najiha, Rozali Annuar, Nur Hazirah
Format: Article
Published: Elsevier Ltd. 2012
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Online Access:http://eprints.utm.my/id/eprint/47553/
http://dx.doi.org/10.1016/j.apcata.2011.11.007
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spelling my.utm.475532019-04-25T01:22:11Z http://eprints.utm.my/id/eprint/47553/ Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst Ruslan, Nurun Najwa Triwahyono, Sugeng Abdul Jalil, Aishah Timmiati, Sharifah Najiha Rozali Annuar, Nur Hazirah QD Chemistry The interaction of molecular hydrogen with the surface of MoO3–ZrO2 was observed using infrared IR and electron spin resonance (ESR) spectroscopy, and the hydrogen adsorption was quantitatively evaluated in the temperature range of 323–573 K. The hydrogen adsorbed IR results confirmed the formation of a new broad band in the range of 3700–3400 cm−1, which corresponds to hydrogen-bonded OH groups. A decrease in the ESR signals indicated the formation of electrons that have been trapped by the electron-deficient metal cations and/or oxygen radicals. The hydrogen adsorbed IR and ESR results suggested that the protons and electrons were formed on the surface of MoO3–ZrO2 from molecular hydrogen enhancing the isomerization of n-heptane. A quantitative study of the hydrogen adsorption showed that the rate of hydrogen uptake was high for the first few minutes at 473 K and above, and the rate reached an equilibrium value within 10 h. At 423 K, different features of the hydrogen adsorption were observed on MoO3–ZrO2, where the hydrogen uptake increased slowly with time and did not reach equilibrium after 10 h. The rate of hydrogen adsorption increased slightly at 373 K and below. Hydrogen adsorption on MoO3–ZrO2 involves two successive steps. The first step involves hydrogen dissociation on a specific site on the MoO3–ZrO2 catalyst to form hydrogen atoms, and the second step involves the surface diffusion of the hydrogen atoms on the MoO3–ZrO2 surface. Then the hydrogen atom becomes a proton by donating an electron to an adjacent Lewis acid site. The rate-controlling step involves the surface diffusion of hydrogen atoms and has an activation energy of 62.8 kJ/mol. A comparison of the hydrogen adsorption on SO42−–ZrO2, WO3–ZrO2 and MoO3–ZrO2 catalysts is discussed. Elsevier Ltd. 2012 Article PeerReviewed Ruslan, Nurun Najwa and Triwahyono, Sugeng and Abdul Jalil, Aishah and Timmiati, Sharifah Najiha and Rozali Annuar, Nur Hazirah (2012) Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst. Applied Catalysis A: General, 413 . pp. 176-182. ISSN 0926-860X http://dx.doi.org/10.1016/j.apcata.2011.11.007 DOI:10.1016/j.apcata.2011.11.007
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic QD Chemistry
spellingShingle QD Chemistry
Ruslan, Nurun Najwa
Triwahyono, Sugeng
Abdul Jalil, Aishah
Timmiati, Sharifah Najiha
Rozali Annuar, Nur Hazirah
Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst
description The interaction of molecular hydrogen with the surface of MoO3–ZrO2 was observed using infrared IR and electron spin resonance (ESR) spectroscopy, and the hydrogen adsorption was quantitatively evaluated in the temperature range of 323–573 K. The hydrogen adsorbed IR results confirmed the formation of a new broad band in the range of 3700–3400 cm−1, which corresponds to hydrogen-bonded OH groups. A decrease in the ESR signals indicated the formation of electrons that have been trapped by the electron-deficient metal cations and/or oxygen radicals. The hydrogen adsorbed IR and ESR results suggested that the protons and electrons were formed on the surface of MoO3–ZrO2 from molecular hydrogen enhancing the isomerization of n-heptane. A quantitative study of the hydrogen adsorption showed that the rate of hydrogen uptake was high for the first few minutes at 473 K and above, and the rate reached an equilibrium value within 10 h. At 423 K, different features of the hydrogen adsorption were observed on MoO3–ZrO2, where the hydrogen uptake increased slowly with time and did not reach equilibrium after 10 h. The rate of hydrogen adsorption increased slightly at 373 K and below. Hydrogen adsorption on MoO3–ZrO2 involves two successive steps. The first step involves hydrogen dissociation on a specific site on the MoO3–ZrO2 catalyst to form hydrogen atoms, and the second step involves the surface diffusion of the hydrogen atoms on the MoO3–ZrO2 surface. Then the hydrogen atom becomes a proton by donating an electron to an adjacent Lewis acid site. The rate-controlling step involves the surface diffusion of hydrogen atoms and has an activation energy of 62.8 kJ/mol. A comparison of the hydrogen adsorption on SO42−–ZrO2, WO3–ZrO2 and MoO3–ZrO2 catalysts is discussed.
format Article
author Ruslan, Nurun Najwa
Triwahyono, Sugeng
Abdul Jalil, Aishah
Timmiati, Sharifah Najiha
Rozali Annuar, Nur Hazirah
author_facet Ruslan, Nurun Najwa
Triwahyono, Sugeng
Abdul Jalil, Aishah
Timmiati, Sharifah Najiha
Rozali Annuar, Nur Hazirah
author_sort Ruslan, Nurun Najwa
title Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst
title_short Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst
title_full Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst
title_fullStr Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst
title_full_unstemmed Study of the interaction between hydrogen and the MOO3-ZRO2 catalyst
title_sort study of the interaction between hydrogen and the moo3-zro2 catalyst
publisher Elsevier Ltd.
publishDate 2012
url http://eprints.utm.my/id/eprint/47553/
http://dx.doi.org/10.1016/j.apcata.2011.11.007
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score 13.188404