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Hydrofinishing catalyst and preparation method thereof

A technology for hydrorefining and catalyst, applied in chemical instruments and methods, physical/chemical process catalyst, chemical/physical process, etc., can solve the problems of short service life of catalyst and low activity of hydrorefining catalyst, and achieve efficient dispersion, The effect of catalyst hydrotreating performance improvement and long service life

Active Publication Date: 2017-05-03
CHINA PETROLEUM & CHEM CORP +1
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  • Description
  • Claims
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Problems solved by technology

[0009] Aiming at the disadvantages of low activity and short service life of the hydrofinishing catalyst in the prior art, the present invention provides a new hydrofinishing catalyst, a preparation method of the hydrofinishing catalyst and the hydrofinishing catalyst prepared by the method, The catalyst prepared by this method not only has significantly improved activity, but also significantly improved the service life of the catalyst

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  • Hydrofinishing catalyst and preparation method thereof
  • Hydrofinishing catalyst and preparation method thereof
  • Hydrofinishing catalyst and preparation method thereof

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preparation example Construction

[0024] The present invention provides a new hydrorefining catalyst and its preparation method. The catalyst comprises a gamma-alumina carrier and an active metal component supported on the gamma-alumina carrier. The active metal component includes nickel and at least A metal element selected from group VIB, the surface of the catalyst has a network structure, the grid density of the network structure is 0.5-50 / square micron, and the grid density is obtained by scanning at least 20 It is determined by the method of calculating the average value of the number of grids distributed in each square micron area in the electron micrograph.

[0025] According to the present invention, preferably, the grid density of the network structure is 5-20 grids / square micron.

[0026] The present invention has no special limitation on the number of photographs taken by the scanning electron microscope, preferably the grid density is determined by calculating the average value of the number of gr...

Embodiment 1

[0068] (1) 75.0g of γ-Al 2 o 3 Carrier (infrared hydroxyl spectrum see figure 2 Middle curve 1) immersed in a solution of 250.0g deionized water, 9.0g urea, 12.0g ammonium nitrate and 14.6g nickel nitrate hexahydrate, heat treated at 85°C for 18 hours, filtered, washed and then dried at 120°C for 3 hours to obtain Ni-modified alumina support, the SEM image of the Ni-modified alumina support is as follows figure 1 As shown, the grid density is listed in Table 1, and the infrared hydroxyl spectrum is shown in figure 2 Middle curve 2. From figure 1 It can be seen that the surface of the Ni-modified alumina support has a large number of network structures. From figure 2 It can be seen that the hydroxyl sites (acidic, basic and neutral) on the surface of the Ni-modified alumina support are much higher than that of γ-Al 2 o 3 Carriers are drastically reduced.

[0069] (2) preparation contains the solution of 39.0g deionized water, 23.4g molybdenum trioxide, 8.4g basic ni...

Embodiment 2

[0083] (1) 75.0g of γ-Al 2 o 3 The carrier was immersed in a solution of 250.0g deionized water, 15.0g urea, 6.7g ammonium nitrate and 36.0g nickel nitrate hexahydrate, heat treated at 90°C for 12 hours, filtered, washed and then dried at 150°C for 2 hours to obtain Ni modified The alumina support, grid density is listed in Table 1.

[0084] (2) preparation contains the solution of 70.0g deionized water, 39.0g molybdenum trioxide, 27.0g basic nickel carbonate and 13.5g phosphoric acid, the alumina carrier of step (1) gained Ni modification is immersed in wherein 1 hour, in Dry at 120°C for 3 hours, and calcinate at 480°C for 2 hours in an air flow of 100 mL / min to obtain catalyst S-2.

[0085] Catalyst S-2 grid density and composition are listed in Table 1.

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Abstract

The invention relates to a hydrofinishing catalyst and a preparation method thereof. The preparation method comprises: (1) immersing a gamma-alumina carrier in a mixture containing urea, a water-soluble neutral nickel salt and water and carrying out heat treatment, filtration, washing and drying to obtain a nickel-modified alumina carrier, and (2) introducing nickel and group VIB metals into the nickel-modified alumina carrier obtained in the step (1), wherein a mole ratio of the water-soluble neutral nickel salt in the step (1) to nickel in the step (2) is 1: 0.2-0.6. The catalyst provided by the invention can realize efficient dispersion of the active component and regulation and control of interaction between the carrier and the active component, effectively solves the problem that the prior art cannot realize coordinated regulation of interaction between active metal dispersed carriers and the active component, and has high catalyst hydrogenation performances and a good industrial application prospect.

Description

technical field [0001] The invention relates to a hydrorefining catalyst, a preparation method of the hydrorefining catalyst and a hydrorefining catalyst prepared by the method. Background technique [0002] Commercial hydrofinishing catalysts generally consist of Group VIII metals (nickel and / or cobalt) and Group VIB metals (molybdenum and / or tungsten) supported on alumina supports, and may also contain some modifying elements or substances. The dispersion state of the active metal of the hydrogenation catalyst directly determines the microstructure and composition of the active phase, the intrinsic activity and the number of active sites, and then determines the activity of the catalyst (see Bergwerff et al., Catal.Today 2008, 130:117). Therefore, how to achieve efficient dispersion of active metals has always been the primary consideration for the preparation of highly active hydrogenation catalysts. [0003] The conventional hydrogenation catalyst preparation process ge...

Claims

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Application Information

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IPC IPC(8): B01J27/19B01J27/188
Inventor 韩伟龙湘云李明丰杨清河聂红
Owner CHINA PETROLEUM & CHEM CORP