3868-66-4Relevant academic research and scientific papers
Nickel-tungsten sulfide aromatic hydrocarbon hydrogenation catalysts synthesized in situ in a hydrocarbon medium
Sizova,Serdyukov,Maksimov
, p. 470 - 480 (2015)
Nickel-tungsten sulfide nanocatalysts for the hydrogenation of aromatic hydrocarbons (HCs) have been prepared by the in situ decomposition of a nickel thiotungstate precursor in a HC feedstock using 1-butyl-1-methylpiperidinium nickel thiotungstate complex [BMPip]2Ni[WS4]2 as the precursor. The in situ synthesized particles have been characterized by X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy. It has been shown that the resulting Ni-W-S particles are nanoplates associated in multilayer agglomerates; the average length of the Ni-W-S particles is 6 nm; the average number of layers in the multilayer packaging is three. The catalytic activity of the synthesized catalysts has been studied in the hydrogenation of model mixtures of mono- and bicyclic aromatic HCs and in the conversion of dibenzothiophene in a batch reactor at a temperature of 350°C and a hydrogen pressure of 5.0 MPa. It has been shown that the studied catalysts can be used for the hydrofining of light cycle oil.
Synthesis of nickel-tungsten sulfide hydrodearomatization catalysts by the decomposition of oil-soluble precursors
Sizova,Kulikov,Onishchenko,Serdyukov,Maksimov
, p. 44 - 50 (2016/02/03)
Nickel-tungsten sulfide catalysts for the hydrogenation of aromatic hydrocarbons have been prepared by the in situ decomposition of an oil-soluble tungsten hexacarbonyl precursor in a hydrocarbon feedstock using oil-soluble nickel salt nickel(II) 2-ethylhexanoate as a source of nickel. The in situ synthesized Ni-W-S catalyst has been characterized by X-ray photoelectron spectroscopy. The activity of the resulting catalysts has been studied in the hydrogenation of bicyclic aromatic hydrocarbons and dibenzothiophene conversion in a batch reactor at a temperature of 350°C and a hydrogen pressure of 5.0 MPa. It has been shown that the optimum W: Ni molar ratio is 1: 2. Using the example of the hydrofining of feedstock with high sulfur and aromatics contents, it has been shown that the synthesized catalyst exhibits high activity in the hydrogenation of aromatic hydrocarbons.
TRANSFORMATIONS OF CYCLOALKANES UNDER THE ACTION OF ACYL HALIDES IN THE PRESENCE OF AlBr3.
Akhrem, I.S.,Orlinkov, A.V.,Mysov, E.I.,Vol'pin, M.E.
, p. 3891 - 3894 (2007/10/02)
Cycloalkanes have been found to react with acyl halides in the presence of AlBr3 ( mole ratio RCOX:AlBr3=1:2 ) under very mild conditions affording products of hydrocarbon oxidative coupling or/and hydrocarbon acylation.
