Nickel-tungsten sulfide aromatic hydrocarbon hydrogenation catalysts synthesized in situ in a hydrocarbon medium
摘要:
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](2)Ni[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 350A degrees 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
作者:I. A. Sizova、A. B. Kulikov、M. I. Onishchenko、S. I. Serdyukov、A. L. Maksimov
DOI:10.1134/s0965544115080174
日期:2016.1
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
Carbon-13 magnetic resonance of hydroaromatics. II. Conformation of Tetralin and tetrahydroanthracene and their methyl derivatives
作者:Frederick G. Morin、W. James Horton、David M. Grant、Don K. Dalling、Ronald J. Pugmire
DOI:10.1021/ja00350a042
日期:1983.6
Carbon-13 chemical shift data have been acquired for 36 methylated tetralins and tetrahydroanthracenes. A least-squares regression analysis has been undertaken on the ring carbons of compounds of unequivocal conformation to determine methyl substituent parameters for the two distinct aliphatic positions and the results have been used to estimate the position of equilibrium of conformationally mobile
Nickel-tungsten sulfide aromatic hydrocarbon hydrogenation catalysts synthesized in situ in a hydrocarbon medium
作者:I. A. Sizova、S. I. Serdyukov、A. L. Maksimov
DOI:10.1134/s0965544115060110
日期:2015.7
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](2)Ni[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 350A degrees 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.
Bailey et al., Journal of the Institute of Petroleum, 1947, vol. 33, p. 511