Nickel system hydrogenation catalyst, preparation method and application

A hydrogenation catalyst and catalyst technology, which is applied in the direction of hydrogenation to hydrocarbons, refining to remove heteroatoms, etc., can solve the problems of poor catalyst stability, dark color, and poor catalyst activity, and achieve good stability and high hydrogenation activity. Effect

Active Publication Date: 2007-09-19
PETROCHINA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these solvent oils have poor properties, deep color, and low economic value. After catalytic hydrogenation, the water-white hydrogenated product oil is obtained as solvent oil or gasoline blending oil.
[0004] U.S. Patent U.S.P 4956328 studies the mixed aqueous solution of nickel, aluminum and zirconium salts. Under the conditions of higher than 60°C and pH value of 7-10, the catalyst is prepared by co-precipitation with basic compounds and is suitable for aromatic hydrocarbons, nitrogen-containing hydrocarbons, and olefins. hydrogenation, the catalyst activity is not good
U.S.P 4307248 has studied the use of alumina and diatomaceous earth as the carrier, and the aqueous solution of the active component nickel and additives magnesium and copper are co-precipitated with basic compounds to prepare a catalyst suitable for the hydrogenation of aromatic hydrocarbons, nitrogen-containing hydrocarbons, and olefins , the catalyst has poor stability

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Dissolve 70.5g of nickel nitrate, 7.5g of aluminum nitrate, 4.5g of zirconium nitrate, and 3.5g of lanthanum nitrate into 300g of water, prepare a mixed aqueous solution, and heat to 50-55°C. Dissolve 15g of ammonium bicarbonate and 30g of potassium carbonate into 300g of water as a precipitating agent. Slowly add the precipitating agent solution to the active component and auxiliary agent solution under full stirring, and then add 10 g of diatomaceous earth. Continue heating the mixed solution to 85° C., adjust the pH value to 8.5 with potassium carbonate aqueous solution, and stir for 1.5 hours. Filter, filter out the mother liquor, and wash the filter cake with distilled water repeatedly 3 to 5 times. The filter cake was dried, extruded, and calcined at 350°C to obtain the catalyst.

[0022] Before hydrogenation, in the hydrogen medium, maintain the temperature of 425 ° C for 15 hours to reduce the catalyst, then cool down to 100 ° C, cool down to 35 ° C with nitro...

Embodiment 2

[0036] Dissolve 60.5g of nickel nitrate, 7.5g of aluminum nitrate, 2.5g of magnesium nitrate, and 5.2g of lanthanum nitrate into 300g of water, prepare a mixed aqueous solution, and heat to 50°C. Dissolve 80ml of ammonia water, 10g of ammonium bicarbonate, and 20g of sodium carbonate into 300g of water as a precipitating agent. Under sufficient stirring, slowly add the precipitating agent solution into the active component and auxiliary agent solution, and then add 10 g of diatomaceous earth. Continue heating the mixed solution to 90° C., adjust the pH value to 9.0 with aqueous sodium carbonate solution, and stir for 1.5 hours. All the other methods are the same as in Example 1. Filter, filter out the mother liquor, and wash the filter cake with distilled water repeatedly 3 to 5 times. The filter cake was dried, extruded, and calcined at 420°C to obtain the catalyst.

[0037] Before hydrogenation, in the hydrogen medium, keep the temperature of 415°C for 16 hours to reduce ...

Embodiment 3

[0045] Dissolve 60.5g of nickel nitrate, 7.5g of aluminum nitrate, 4.5g of copper nitrate, 3.5g of magnesium nitrate, and 2.5g of lanthanum nitrate into 300g of water, prepare a mixed aqueous solution, and heat to 50°C. Dissolve 50ml of ammonia water, 5g of ammonium bicarbonate, and 30g of sodium carbonate into 300g of water as a precipitating agent. Under sufficient stirring, slowly add the precipitating agent solution into the active component and auxiliary agent solution, and then add 10 g of diatomaceous earth. Continue heating the mixed solution to 80° C., adjust the pH value to 8.5 with aqueous sodium carbonate solution, and stir for 1.5 hours. Filter, filter out the mother liquor, and wash the filter cake with distilled water repeatedly 3 to 5 times. The filter cake was dried, extruded, and calcined at 390°C to obtain the catalyst.

[0046] Before hydrogenation, in the hydrogen medium, maintain the temperature of 385 ° C for 25 hours to reduce the catalyst, then cool ...

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Abstract

The invention realtes to a nickel based hydrogenation catalyst, preparation and application thereof. Using alumina or and monox silica as carrier, the catalyst prepared by means of coprecipitation, main containing active component Ni, is characterized in catalyst composed by active component Ni, La, adjuvant X1 and carrier X2O. Calculated by weight of component, the catalyst including: NiO 40-70%, La2O3 2-5%, X2O 20-50%, wherein X1 is selected from one or more of Cu, Mg, Zr, X2 is selected from Al or and Si; surface area to volume ratio thereof is 80-200 m<2>/g, pore volume ratio is 0.4-0.8 ml/g. The catalyst is suit for mono olefin hydrogenation, especially for hydrogenation of pyrolysis C9 distillation, which has higher hydrogenation activity, definited sulfur poison resist and carboid resist to fit for higher require of high colloid raw material hydrogenation which of catalyst has high hydrogenation activity and good stability.

Description

technical field [0001] The invention relates to a nickel-based hydrogenation catalyst and its preparation method and application. The catalyst is suitable for the hydrogenation of monoolefins, especially for the cracking of C 9 Hydrogenation of distillates. Background technique [0002] Ethylene cracking fractions often contain a certain amount of inorganic sulfur and coke, causing catalyst poisoning and deactivation. In addition, heavier cracking fractions such as: cracking C 9 The depth of hydrogenation is not enough when precious metal catalysts are used for distillate hydrogenation, and the hydrogenation temperature is too high when molybdenum-nickel and cobalt-molybdenum catalysts are used, resulting in severe coking. For this reason, a new type of nickel-based catalyst with certain sulfur resistance, coke resistance and high hydrogenation performance has been developed, and it is used in the hydrogenation of medium and low cracking fractions. [0003] cleavage C 9 ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C10G45/06C07C5/03
Inventor 梁顺琴肖春景董海明谢元马红江
Owner PETROCHINA CO LTD
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