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Preparation method of hydrocarbon hydrogenation catalyst

A hydrogenation catalyst, alumina technology, applied in the direction of molecular sieve catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problem of amorphous silicon-aluminum agglomeration, easy access to each other's channels or blocking molecular sieves, hydrogenation function and Cracking function does not match and other problems, to achieve the effect of improving performance

Active Publication Date: 2014-05-21
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Among them, the carrier material is prepared by directly adding molecular sieves in the process of forming amorphous silica-alumina. In this way, amorphous silica-alumina is prone to agglomeration, and it is also easy to enter the pores of the other party or block the pores of molecular sieves, which affects the amorphous silica-alumina. The distribution on the molecular sieve, the poor connectivity between the molecular sieve and the amorphous silica-alumina channel, reduces the specific surface area and pore volume of the catalyst, and the distribution of active metals is not easy to control, which makes the hydrogenation function of the catalyst mismatch with the cracking function, affecting the catalyst performance

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0041] Add 555g of solid aluminum chloride and 153g of nickel nitrate hexahydrate into 10 liters of distilled water while heating and stirring until dissolved to obtain solution (a). Add an appropriate amount of distilled water to the concentrated ammonia water and dilute it into about 10wt% dilute ammonia water (b), and dissolve 42.5g of 1,5-pentanediol in 2L of water to form a solution (c). 27g Y-type molecular sieve Y-1 (SiO 2 / Al 2 o 3 The molar ratio is 11.0, the unit cell constant is 24.42?, and the relative crystallinity is 95%) use impregnation solution containing 174g sodium tungstate for saturated impregnation, after impregnation, dry at 120°C for 180 minutes, and bake at 500°C for 4 hours; 10.5g Dissolve diamine in 300ml of absolute ethanol, heat to 60°C, stir for half an hour, add metal-modified Y molecular sieve, continue stirring for 2 hours, obtain modified molecular sieve (d) that pre-adsorbs organic amine after filtration. Take a plastic tank, add (a) into ...

Embodiment 2

[0044] Add 555g of solid aluminum sulfate and 148g of nickel nitrate into 10 liters of distilled water while heating and stirring until dissolved to obtain solution (a). Dilute the concentrated ammonia water with an appropriate amount of distilled water to obtain about 10wt% dilute ammonia water (b), and dissolve 82g of 1,4-butanediol in 1L of water to obtain a solution (c). 166g Y-type molecular sieve Y-1 (SiO 2 / Al 2 o 3 The molar ratio is 11.0, the unit cell constant is 24.42?, and the relative crystallinity is 95%) use impregnation solution containing 168g sodium tungstate for saturated impregnation, after impregnation, dry at 120°C for 180 minutes, and bake at 500°C for 4 hours; The amine was dissolved in 5 L of water, heated to 60° C., stirred for half an hour, and the metal-modified molecular sieve was added and stirred for 2 hours to obtain a molecular sieve slurry (d). Take a plastic tank, add (a) into the tank, stir and heat to 60°C, open the valve of the containe...

Embodiment 3

[0047] Add 555g of solid aluminum sulfate and 767g of nickel nitrate into 10 liters of distilled water while heating and stirring until dissolved to obtain solution (a). Prepare the solid sodium metaaluminate to a concentration of 20g Al 2 o 3 / l sodium aluminate solution (b), 198.4g propylene glycol is dissolved in 1L water to form solution (c). 1543g Y-type molecular sieve Y-1 (SiO 2 / Al 2 o 3 The molar ratio is 11.0, the unit cell constant is 24.42?, and the relative crystallinity is 95%) use an impregnation solution containing 870g sodium tungstate for saturated impregnation, dry at 120°C for 180 minutes after impregnation, and roast at 500°C for 4 hours; 155g diethanolamine Dissolve in 10L of water, heat to 60°C, add the metal-modified molecular sieve under stirring, continue stirring at the temperature for 2 hours, and filter to obtain the treated molecular sieve (d). Take a glue tank, put 2l of deionized water into it, stir and heat to 60°C, then add (d), at the sa...

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PUM

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Abstract

The invention discloses a preparation method of a hydrocarbon hydrogenation catalyst. The method comprises the following steps: adding a mixture of group VIII metal cation modified molecular sieves and organic amines as well as organic alcohols and / or organic acids before or in the process of preparing an alumina-group VIB metal oxide composite oxide by a coprecipitation method; carrying out aging after gel forming is completed and then obtaining a catalyst intermediate through filtration, washing and drying; then carrying out forming, drying and roasting, thus obtaining the hydrogenation catalyst. The catalyst prepared by the method can organically combine the molecular sieves and alumina together with good combination degree and dispersion degree, thereby avoiding agglomeration and even blockage of the molecular sieves and amorphous alumina, simultaneously controlling the distribution of hydrogenation components on various acidic components effectively and improving the usability of the catalyst; and the catalyst is especially suitable for the hydrocarbon hydro-upgrading process with moderate requirements for acidity and the hydrogenation function.

Description

technical field [0001] The invention relates to a method for preparing a hydrogenation catalyst, in particular to a method for preparing a hydrogenation catalyst containing molecular sieves. Background technique [0002] Hydrocracking technology is one of the important means for the secondary processing of crude oil and the lightening of heavy oil. Because of its strong adaptability to raw materials, flexible production operations and product solutions, and good product quality, it has become an important way to produce high-quality light clean oil products and solve the source of chemical raw materials. [0003] Hydrocracking catalysts are generally dual-functional catalysts, and their cracking activity and hydrogenation activity are respectively provided by the acidic component and hydrogenation active component in the catalyst. [0004] The acidic component of the catalyst is generally provided by molecular sieves contained in the catalyst and / or refractory inorganic oxi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J29/16B01J29/78
Inventor 蒋广安刘雪玲李宝忠张晔郑庆华王继锋
Owner CHINA PETROLEUM & CHEM CORP
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