Preparation method of hydrocracking catalyst

A hydrocracking and catalyst technology, applied in physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of poor catalyst performance, poor product stability, complex preparation process, etc., to increase the probability of cracking, improve Acidic structure, the effect of reducing the cost of use

Active Publication Date: 2013-07-10
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although this type of catalyst has high hydrogenation performance, the pore volume and specific surface area of ​​the catalyst are relatively small, and generally it can only process lighter fractions below diesel oil, and because the metal utilization rate of the catalyst prepared by the co-precipitation method is low, the metal dispersion performance Not good, and the preparation process is complicated, and the product stability is poor, so the catalyst is not cost-effective
[0009] The kneading method can also prepare catalysts with various active metal contents, but the performance of the catalyst prepared by the kneading method is relatively poor, the effective utilization rate of the active metal is low, and the hydrogenation catalyst is rarely prepared by the kneading method in industrial production.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] Take 1000g of alumina dry rubber powder and carry out water vapor treatment. The hydrothermally treated alumina is obtained under the gauge pressure of 0.05MPa, the hydrothermal treatment temperature is 45°C, the treatment time is 1.5 hours, and the volume ratio of ammonia gas and water vapor is 10%. The water content of the dry rubber powder is 35wt%, the pore volume is 1.1mL / g, and the specific surface area is 445m 2 / g, numbered LA-1.

Embodiment 2

[0042] Take 1000g of alumina dry rubber powder and carry out water vapor treatment. Under the gauge pressure of 0.08MPa, the hydrothermal treatment temperature is 75°C, the treatment time is 2 hours, and the volume ratio of ammonia gas and water vapor is 15%. The water content of the rubber powder is 43wt%, the pore volume is 1.15mL / g, and the specific surface area is 415m 2 / g, numbered LA-2.

[0043] Example 2

[0044] Take 1000g of alumina dry rubber powder for water vapor treatment, at a gauge pressure of 0.1MPa, a hydrothermal treatment temperature of 90°C, a treatment time of 3 hours, and a volume ratio of ammonia gas to water vapor of 20%, to obtain hydrothermally treated alumina The water content of the dry rubber powder is 50wt%, the pore volume is 1.17mL / g, and the specific surface area is 410m 2 / g, numbered LA-3.

Embodiment 4

[0046] Taking the tungsten-nickel system as an example, the preparation of the catalyst is carried out.

[0047] Prepare an impregnation solution containing tungsten and nickel with a concentration of 25.5g metal (calculated as oxide) / 100mL solution, impregnate at a temperature of 30°C, and a liquid-solid ratio of 4:1, impregnate 200g of LA-1 aluminum hydroxide dry rubber powder, impregnate The drying time was 2.5 hours, dried at 120°C for 8 hours, and crushed into 180 mesh to obtain an alumina dry rubber powder mixture containing active metal components (dry basis: 74.3wt%).

[0048] Take the above-mentioned alumina dry rubber powder mixture containing active metal components, 509g of Y-1 molecular sieve (85wt% on a dry basis) and 144.5 grams of binder (30wt% on a dry basis, the molar ratio of nitric acid to small-pore alumina is 0.3 ) into a rolling machine for mixing, adding water, rolling into a paste, and extruding into a cylinder with a diameter of 1.8mm. Dry at 120°C f...

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Abstract

The invention discloses a preparation method of a hydrocracking catalyst. The preparation method comprises the following steps of carrying out low-temperature hydro-thermal treatment on alumina dry gel powder in the ammonia-containing water vapor atmosphere, dipping the alumina dry gel powder subjected to hydro-thermal treatment into a solution containing a hydrogenation active metal ingredient, carrying out drying, and carrying out full grinding, molding, drying and calcination of the alumina dry gel powder with the hydrogenation active metal ingredient, and a molecular sieve in the presence of a peptizer or a binder to obtain the hydrocracking catalyst. The preparation method improves a catalyst pore structure. The hydrocracking catalyst obtained by the preparation method has a large specific surface area and a large pore volume, is conducive to optimized cooperation of a hydrogenation ingredient and a cracking ingredient, has high catalytic activity, and is suitable for hydrocracking yield-increasing of high-quality heavy naphtha from vacuum distillate having a high dry point and poor quality and for a catalytic process for improvement of tail oil product quality.

Description

technical field [0001] The invention relates to a method for preparing a hydrocracking catalyst, in particular to a method for preparing a hydrocracking catalyst for heavy distillate oil. Background technique [0002] Hydrocracking technology has the characteristics of strong adaptability of raw materials, great flexibility of product schemes, high selectivity of target products, good product quality, and high added value. It can directly convert various heavy and low-quality raw materials into clean fuel oil and high-quality chemical raw materials. It has become one of the most important heavy oil deep processing techniques in modern oil refining and petrochemical industries, and has been increasingly widely used at home and abroad. Although the processing capacity of my country's existing hydrocracking units has exceeded 50.0Mt / a, due to the deterioration of domestic crude oil quality year by year, the import of high-sulfur crude oil has increased significantly, and enviro...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J29/16B01J35/10C10G47/20
Inventor 刘昶王凤来杜艳泽赵红关明华
Owner CHINA PETROLEUM & CHEM CORP
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