Preparation method of bulk phase hydrocracking catalyst

A cracking catalyst and hydrocracking technology, applied in physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve problems such as ammonia nitrogen pollution, environmental pollution, and poor cohesiveness of catalyst materials, and improve acidity and acidity distribution, avoiding ammonia nitrogen pollution, and reducing the effect of secondary cracking

Active Publication Date: 2015-05-13
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Most of the existing co-precipitation methods for preparing catalysts use NH3·H2O as a precipitating agent, which will produce a large amount of wastewater containing ammonia and nitrogen, causing pollution to the environment
[0007] The hydrocracking catalyst disclosed in US 3954671, the hydroconversion catalyst disclosed in US 4313817, the hydrocracking catalyst disclosed in CN1253988A, the nitrogen-resistant type prolific middle distillate oil, the heavy hydrocarbon hydrocracking catalyst disclosed in CN1253989A, these catalysts are Prepared by the co-gel method, the alkaline precipitant used is all ammonia, although a hydrocracking catalyst with ideal performance for the treatment of heavy hydrocarbons and prolific middle distillates can be obtained, the pollution caused by ammonia nitrogen to the environment is not significant. Too effective governance measures
CN101239324A discloses a method for preparing a high-activity, high-medium oil type hydrocracking catalyst by a co-gel method. The precipitant uses a weakly basic ammonia compound, and there is still the problem of ammonia nitrogen pollution
[0008] What CN101172261A discloses is to adopt sodium metaaluminate alkali solution as the method for precipitating agent to prepare hydrogenation catalyst, and precipitation mainly comes from metaaluminate ion and hydroxide ion, like this easily forms larger precipitation particle in precipitation process, and catalyst material The cohesiveness of the catalyst is poor, and the specific surface area and strength of the catalyst are reduced, which will affect the performance of the catalyst.
If sodium metaaluminate replaces aluminum chloride, aluminum nitrate, aluminum sulfate and other soluble inorganic aluminum salts as the aluminum source, a large amount of NO3-, Cl-, SO42- and other hetero ions, the prepared composite oxide precursors have poor peptization and difficult to form metal materials
Another difficulty in the preparation of catalysts by the co-precipitation method is that the grain size of the metal mixture obtained by different aluminum sources and precipitants varies greatly, which in turn has a great impact on the specific surface area and strength of the catalyst.
In order to reduce pollution, how to solve the problem of poor cohesion of materials produced by the bulk phase cleaning preparation method using sodium metaaluminate instead of ammonia water as precipitant

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Concrete preparation steps are as follows:

[0031] (1) Preparation of acidic solution A: 230 ml of nickel chloride solution containing NiO of 150 g / l, containing WO 3 75g / l ammonium metatungstate 1050ml with ZrO 2 150 milliliters of 120 g / l zirconium oxychloride solution was mixed in a 5-liter container, then 200 grams of butanediol was added, and then 800 milliliters of clean water was added for dilution. Formulated with SiO 2 Add 520 milliliters of 80 g / l dilute water glass solution to the above mixed salt solution under stirring;

[0032] (2) Configure alkaline sodium metaaluminate solution B: configure Al 2 o 3 The concentration is 26g / l alkaline solution 2800ml;

[0033] (3) Add 1000mL of clean water into the gelling tank, and pass CO2 with a volume concentration of 85v% into the clean water 2 , so that the CO in the gas in the tank 2 The concentration is 80v%, sealed tank;

[0034] (4) Put solution A and solution B into the glue tank in parallel to for...

Embodiment 2

[0038] According to the method of embodiment 1, press the component content ratio of catalyst B in table 1, add 150 grams of tetraethylammonium bromide in the acidic solution, prepare catalyst B, just transfer the gelling temperature to 65 ℃, to adjust the hole structure, the pH value at the end was controlled to be 7.8, and the composition and main properties of the catalyst are shown in Table 1.

Embodiment 3

[0040] According to the method of embodiment 2, press the component content ratio of catalyst C in table 1, add 250 grams of ethylene glycol in the acidic solution, prepare catalyst C, just change zirconium oxychloride into titanium tetrachloride. The catalyst composition and main properties are shown in Table 1.

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Abstract

The invention discloses a preparation method of a bulk phase hydrocracking catalyst. The method comprises the steps of preparing an acidic mixed solution A containing hydrogenation reactive metals, silicon and organic solvents, and preparing a sodium metaaluminate alkaline solution B; filling clear water into a reaction tank and filling CO2 into the clear water; and then adding the acidic mixed solution A and the alkaline solution B to the reaction tank in parallel to prepare gel, controlling the pH value of pulp in the reaction tank to be 7.0-9.0, then adding turbid liquid of a Y type molecular sieve, mixing the substances uniformly, filtering and drying the obtained mixture, and then forming, washing, drying and roasting the filter cake, thus preparing the hydrocracking catalyst. The catalyst prepared by the method has the advantages of big specific surface area, big pore volume, high strength and high dispersibility of reactive metal components, and is especially suitable to serve as a high-activity middle oil type hydrocracking catalyst.

Description

technical field [0001] The invention relates to a preparation method of a hydrocracking catalyst for treating heavy hydrocarbons, in particular to a preparation method of a high-activity high-medium oil type body-phase hydrocracking catalyst. Background technique [0002] At present, the shortage of petroleum resources in the world, the quality of crude oil is deteriorating year by year, the demand for middle distillate oil is increasing, the upgrading of petrochemical products and the stricter environmental regulations have greatly promoted the transformation of heavy oil into lighter products, and constituted an accelerated development of hydrogenation. The power of technology. The main features of hydrocracking technology are strong adaptability of raw materials, high selectivity of product plans and target products, good product quality and high added value, and can directly produce a variety of high-quality petroleum products (such as gasoline, jet fuel, diesel oil, lub...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J29/16C10G47/20
Inventor 王海涛徐学军刘东香王继锋冯小萍
Owner CHINA PETROLEUM & CHEM CORP
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