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rdf:type
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Description
| - Recent catalysts of hydrodesulfurization (HDS) reaction consist of CoMo and NiMo phase supported on gamma-Al2O3 support. The support was modified with cobalt nitrate, nickel nitrate, or boric acid and high loadings of Anderson type heteropolyoxomolybdate (NH4)3[Ni(OH)6Mo6O18].7H2O were deposited. Surface area (SBET) and sulfide phase dispersion of the catalysts were determined by N2 physisorption and O2 chemisorption, respectively. Samples were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, infrared and UV-Vis spectrometry, and temperature programmed reduction. The activity of catalyst was measured in HDS of 1-benzothiophene. The preliminary incorporation of Co, Ni and B into the support increased the HDS activity of the deposited NiMo phase. IR and UV-Vis DR data revealed the partial decomposition of the initial Anderson type NiMo complex with a formation of new surface compounds, including heteropolymolybdates and separated polymeric oxomolybdenum compounds. X-ray photoelectron spectroscopy showed that the degree of Mo sulfidation is the smallest for the catalysts prepared over unmodified alumina and boron-modified alumina. The highest degree of sulfidation was found for the catalysts supported over Co-and Ni-modified alumina. The nickel-modified alumina increased the HDS activity and dispersion of the NiMo phase the most, which was associated with the formation of the largest number of active sites.
- Recent catalysts of hydrodesulfurization (HDS) reaction consist of CoMo and NiMo phase supported on gamma-Al2O3 support. The support was modified with cobalt nitrate, nickel nitrate, or boric acid and high loadings of Anderson type heteropolyoxomolybdate (NH4)3[Ni(OH)6Mo6O18].7H2O were deposited. Surface area (SBET) and sulfide phase dispersion of the catalysts were determined by N2 physisorption and O2 chemisorption, respectively. Samples were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, infrared and UV-Vis spectrometry, and temperature programmed reduction. The activity of catalyst was measured in HDS of 1-benzothiophene. The preliminary incorporation of Co, Ni and B into the support increased the HDS activity of the deposited NiMo phase. IR and UV-Vis DR data revealed the partial decomposition of the initial Anderson type NiMo complex with a formation of new surface compounds, including heteropolymolybdates and separated polymeric oxomolybdenum compounds. X-ray photoelectron spectroscopy showed that the degree of Mo sulfidation is the smallest for the catalysts prepared over unmodified alumina and boron-modified alumina. The highest degree of sulfidation was found for the catalysts supported over Co-and Ni-modified alumina. The nickel-modified alumina increased the HDS activity and dispersion of the NiMo phase the most, which was associated with the formation of the largest number of active sites. (en)
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Title
| - Hydrodesulfurization NiMo Catalysts Supported on Co, Ni and B Modified Al2O3 from Anderson Heteropolymolybdates
- Hydrodesulfurization NiMo Catalysts Supported on Co, Ni and B Modified Al2O3 from Anderson Heteropolymolybdates (en)
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skos:prefLabel
| - Hydrodesulfurization NiMo Catalysts Supported on Co, Ni and B Modified Al2O3 from Anderson Heteropolymolybdates
- Hydrodesulfurization NiMo Catalysts Supported on Co, Ni and B Modified Al2O3 from Anderson Heteropolymolybdates (en)
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skos:notation
| - RIV/67985858:_____/12:00383060!RIV13-GA0-67985858
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/67985858:_____/12:00383060
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - NiMo/γ-Al2O3; anderson heteropolymolybdate; additives (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Kaluža, Luděk
- Jirátová, Květa
- Palcheva, R.
- Spojakina, A.
- Tyuliev, G.
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issn
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number of pages
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http://bibframe.org/vocab/doi
| - 10.1016/j.proeng.2012.07.480
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