Catalytic cracking catalyst and preparation method thereof

A catalytic cracking and catalyst technology, which is applied in the direction of physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problem of low gasoline yield, and achieve the reduction of heavy oil yield, the improvement of cracking performance, and the increase of gasoline yield Effect

Active Publication Date: 2018-04-13
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The molecular sieve obtained by this method is used for catalytic cracking, and the gasoline yield is not high

Method used

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  • Catalytic cracking catalyst and preparation method thereof
  • Catalytic cracking catalyst and preparation method thereof
  • Catalytic cracking catalyst and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] 27.9g zirconium nitrate Zr(NO 3 ) 4 ·5H 2 O was dissolved in 500g deionized water, stirred evenly, adjusted the pH value of the mixture to 4.5 with dilute ammonia water, then raised the temperature to 40°C, and continued to stir for 60min; take 200g (dry basis weight) of DY1-1 molecular sieve provided in Comparative Example 1 and add into the above mixture, stirred at 40°C for 2 hours; after filtration, the obtained filter cake was roasted at 650°C and 100% water vapor for 2 hours to obtain a zirconium-modified Y molecular sieve, denoted as Y1, and its properties are shown in Table 1 . After the Y1 molecular sieve was aged at 800°C and 100% water vapor for 17 hours, its crystallinity and specific surface area were measured, and the crystallization retention and specific surface area retention were calculated. The results are listed in Table 1.

[0041] The cracking catalyst was prepared according to the method of Comparative Example 1, except that an equal amount of ...

Embodiment 2

[0043] Dissolve 51.2g of tetrabutyl titanate in 800g of deionized water, stir evenly, adjust the pH value of the mixture to 6.0 with dilute ammonia water, then stir at room temperature for 30min; take 200g of DY1-1 molecular sieve provided in Comparative Example 1 (dry Basis weight) was added to the above mixture, heated to 60°C, and continued to stir for 1 hour; after filtration, the resulting filter cake was roasted at 500°C and 100% water vapor for 3 hours to obtain a titanium-modified Y molecular sieve, denoted as Y2 , whose properties are shown in Table 1. After the Y2 molecular sieve was aged at 800°C and 100% water vapor for 17 hours, its crystallinity and specific surface area were measured, and the crystallization retention and specific surface area retention were calculated. The results are listed in Table 1.

[0044] The cracking catalyst was prepared according to the method of Comparative Example 2, except that an equal amount of Y2 molecular sieve was used instead...

Embodiment 3

[0046] 5.2g zirconium oxychloride ZrOCl 2 ·8H 2 Dissolve O in 1800g deionized water, stir well, adjust the pH value of the mixture to 7.0 with dilute ammonia water, raise the temperature to 80°C, and stir for 20min; take 200g (dry weight) of DASY (0.0) molecular sieves and add them to the above mixture, at 80 Stir at °C for 2 hours; filter, and roast the obtained filter cake at 450°C and 100% steam for 5 hours to obtain a zirconium-modified Y molecular sieve, denoted as Y3, and its properties are shown in Table 1. After the Y3 molecular sieve was aged at 800°C and 100% water vapor for 17 hours, its crystallinity and specific surface area were measured, and the crystallization retention and specific surface area retention were calculated. The results are listed in Table 1.

[0047]Mix 323g of pseudo-boehmite and 1478g of deionized water, stir for 30 minutes to obtain a pseudo-boehmite slurry, adjust the pH of the slurry to 3.8 with dilute hydrochloric acid, and age at 60°C for...

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Abstract

A catalytic cracking catalyst and a preparation method thereof, based on the total weight of the catalyst, the catalyst contains 10-60% by weight of titanium and / or zirconium modified Y molecular sieve, 10-60% by weight of clay and 5-50% by weight of Binder; the titanium and / zirconium modified Y molecular sieve contains 1.0% to 15.0% by weight of titanium and / zirconium metal oxides. The catalyst preparation method includes the steps of preparing titanium and / or zirconium modified Y molecular sieve, preparing catalyst slurry and spray drying, wherein the titanium and / or zirconium modified Y molecular sieve includes the following steps: (1) adding titanium and / or The zirconium compound is dispersed in water, and the pH value of the mixture is adjusted to 3 to 10; (2) the molecular sieve is mixed with the mixture obtained in step (1), and stirred; optionally filtered and / or dried; (3) calcined at 300 to 700° C. . The catalyst has high heavy oil conversion capacity and gasoline yield.

Description

technical field [0001] The present invention relates to a hydrocarbon catalytic cracking catalyst and its preparation method, more specifically to a catalytic cracking catalyst containing titanium and / or zirconium and its preparation method. Background technique [0002] With the increasingly heavy catalytic cracking raw oil, it is required that the catalytic cracking catalyst should have higher activity and higher hydrothermal stability at the same time, so as to improve the conversion of heavy oil and the ability to resist heavy metal pollution. Therefore, the main The active group member Y molecular sieve has high thermal and hydrothermal stability, and maintains a suitable distribution of acidic active centers. In order to obtain the Y molecular sieve with the above properties, the artificially synthesized NaY molecular sieve is usually modified. Commonly used modification methods include ion exchange, ultra-stabilization treatment, and rare earth modification. Among t...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J29/08B01J29/16C10G47/20
Inventor 于善青王振波田辉平许明德
Owner CHINA PETROLEUM & CHEM CORP
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