About: Hydrodesulfurization NiMo Catalysts Supported on Co, Ni and B Modified Al2O3 from Anderson Heteropolymolybdates     Goto   Sponge   NotDistinct   Permalink

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  • 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)
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)
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)
skos:notation
  • RIV/67985858:_____/12:00383060!RIV13-GA0-67985858
http://linked.open...avai/riv/aktivita
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  • I, P(GAP106/11/0902)
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  • 140010
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  • RIV/67985858:_____/12:00383060
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  • NiMo/γ-Al2O3; anderson heteropolymolybdate; additives (en)
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  • NL - Nizozemsko
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  • [0FD7BF38C214]
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  • Procedia Engineering
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  • 42
http://linked.open...iv/tvurceVysledku
  • Kaluža, Luděk
  • Jirátová, Květa
  • Palcheva, R.
  • Spojakina, A.
  • Tyuliev, G.
issn
  • 1877-7058
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.proeng.2012.07.480
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