Thermal characterisation of molybdenum and platinum-molybdenum catalysts
Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in...
Ausführliche Beschreibung
Autor*in: |
Sarbak, Z. [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
2007 |
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Schlagwörter: |
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Anmerkung: |
© Springer-Verlag 2007 |
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Übergeordnetes Werk: |
Enthalten in: Journal of thermal analysis and calorimetry - Kluwer Academic Publishers, 1998, 87(2007), 1 vom: Jan., Seite 229-232 |
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Übergeordnetes Werk: |
volume:87 ; year:2007 ; number:1 ; month:01 ; pages:229-232 |
Links: |
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DOI / URN: |
10.1007/s10973-006-7817-6 |
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Katalog-ID: |
OLC2049782403 |
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520 | |a Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. | ||
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10.1007/s10973-006-7817-6 doi (DE-627)OLC2049782403 (DE-He213)s10973-006-7817-6-p DE-627 ger DE-627 rakwb eng 660 VZ Sarbak, Z. verfasserin aut Thermal characterisation of molybdenum and platinum-molybdenum catalysts 2007 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 2007 Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. Mo/Al O Pt-Mo/Al O catalysts TPR–CO TPR–H Jóźwiak, W. K. aut Enthalten in Journal of thermal analysis and calorimetry Kluwer Academic Publishers, 1998 87(2007), 1 vom: Jan., Seite 229-232 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:87 year:2007 number:1 month:01 pages:229-232 https://doi.org/10.1007/s10973-006-7817-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 87 2007 1 01 229-232 |
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10.1007/s10973-006-7817-6 doi (DE-627)OLC2049782403 (DE-He213)s10973-006-7817-6-p DE-627 ger DE-627 rakwb eng 660 VZ Sarbak, Z. verfasserin aut Thermal characterisation of molybdenum and platinum-molybdenum catalysts 2007 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 2007 Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. Mo/Al O Pt-Mo/Al O catalysts TPR–CO TPR–H Jóźwiak, W. K. aut Enthalten in Journal of thermal analysis and calorimetry Kluwer Academic Publishers, 1998 87(2007), 1 vom: Jan., Seite 229-232 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:87 year:2007 number:1 month:01 pages:229-232 https://doi.org/10.1007/s10973-006-7817-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 87 2007 1 01 229-232 |
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10.1007/s10973-006-7817-6 doi (DE-627)OLC2049782403 (DE-He213)s10973-006-7817-6-p DE-627 ger DE-627 rakwb eng 660 VZ Sarbak, Z. verfasserin aut Thermal characterisation of molybdenum and platinum-molybdenum catalysts 2007 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 2007 Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. Mo/Al O Pt-Mo/Al O catalysts TPR–CO TPR–H Jóźwiak, W. K. aut Enthalten in Journal of thermal analysis and calorimetry Kluwer Academic Publishers, 1998 87(2007), 1 vom: Jan., Seite 229-232 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:87 year:2007 number:1 month:01 pages:229-232 https://doi.org/10.1007/s10973-006-7817-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 87 2007 1 01 229-232 |
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10.1007/s10973-006-7817-6 doi (DE-627)OLC2049782403 (DE-He213)s10973-006-7817-6-p DE-627 ger DE-627 rakwb eng 660 VZ Sarbak, Z. verfasserin aut Thermal characterisation of molybdenum and platinum-molybdenum catalysts 2007 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 2007 Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. Mo/Al O Pt-Mo/Al O catalysts TPR–CO TPR–H Jóźwiak, W. K. aut Enthalten in Journal of thermal analysis and calorimetry Kluwer Academic Publishers, 1998 87(2007), 1 vom: Jan., Seite 229-232 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:87 year:2007 number:1 month:01 pages:229-232 https://doi.org/10.1007/s10973-006-7817-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 87 2007 1 01 229-232 |
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Thermal characterisation of molybdenum and platinum-molybdenum catalysts |
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Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. © Springer-Verlag 2007 |
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Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. © Springer-Verlag 2007 |
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Abstract Alumina supported Mo and Pt-Mo catalysts was subject to temperature programmed reduction (TPR) using $ H_{2} $ and CO. After earlier oxidation step TPR–$ H_{2} $ profiles shows different surface species, which depends on the composition of the catalysts and reduction temperature. Change in reducing gas from $ H_{2} $ into CO results in significant changes in catalyst system. Hydrogen causes a decrease in oxidation number of metals, while carbon monoxide reacts with chemisorbed chemicals. © Springer-Verlag 2007 |
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K.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of thermal analysis and calorimetry</subfield><subfield code="d">Kluwer Academic Publishers, 1998</subfield><subfield code="g">87(2007), 1 vom: Jan., Seite 229-232</subfield><subfield code="w">(DE-627)244148767</subfield><subfield code="w">(DE-600)1429493-X</subfield><subfield code="w">(DE-576)066397693</subfield><subfield code="x">1388-6150</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:87</subfield><subfield code="g">year:2007</subfield><subfield code="g">number:1</subfield><subfield code="g">month:01</subfield><subfield code="g">pages:229-232</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/s10973-006-7817-6</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">87</subfield><subfield code="j">2007</subfield><subfield code="e">1</subfield><subfield code="c">01</subfield><subfield code="h">229-232</subfield></datafield></record></collection>
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