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Method for utilizing residues of catalyst production

A catalyst and waste residue technology, applied in the field of waste residue utilization, can solve the problems of low cracking capacity of heavy oil, poor hydrothermal stability, poor selectivity of coke and dry gas, etc., and achieve good hydrothermal stability, high yield, The effect of high activity stability

Active Publication Date: 2014-08-20
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, although the catalyst prepared by this method has a relatively high initial activity of light oil micro-reaction, the hydrothermal stability is not good, the activity decreases rapidly after a long time of aging, the cracking ability of heavy oil is not high, and the selectivity of coke and dry gas is poor.

Method used

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  • Method for utilizing residues of catalyst production
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  • Method for utilizing residues of catalyst production

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preparation example Construction

[0025] In the preparation method of active carrier provided by the invention, ammonium salt or alkali metal salt is used to exchange in step (3), and the conditions of exchange include: the temperature of exchange is 30~80 ℃, the exchange time is 0.2~2 hours, waste residue (on a dry basis The weight ratio of ammonium salt (or alkali metal salt) to ammonium salt (or alkali metal salt) is 10-20:1, the pH value is 2-4, and the weight ratio of water and waste residue in the exchange solution is 5-20:1. The calcination time in step (3) is 1-2 hours; the calcination temperature is preferably 500-700°C. The ammonium salt is preferably ammonium chloride and / or ammonium nitrate, and the alkali metal salt is preferably sodium chloride or sodium nitrate. The washing is an existing method, such as washing with deionized water, usually according to the waste residue solid after exchange: water=1:5~20 ratio washing, to remove the free heteroions exchanged, the temperature can be normal temp...

Embodiment approach

[0027]The preparation method of the active carrier provided by the invention, a specific embodiment, comprises:

[0028] (1) drying the waste catalyst residue at 100-150° C. for 1-5 hours;

[0029] (2) The material obtained in step (1) is contacted with ammonium salt for ion exchange, and then washed, the exchange temperature is 30~80°C, and the exchange time is 0.2~2 hours. The weight ratio is 5-10:1, and the pH is 2.0-3.0.

[0030] (3) Roasting the material obtained in step (2) for 1 to 2 hours at 500 to 700°C, then washing and filtering, the exchange temperature is 30 to 80°C, and the exchange time is 0.2 to 2 hours. Waste residue (on a dry basis) and The weight ratio of the ammonium salt is 10-20:1, and the pH is 2.0-4.0.

[0031] (4) mixing the material obtained in step (3) with wet or dry molecular sieve waste residue and water for beating, then filtering and drying at 100-150°C for 2-5 hours, and then roasting, the roasting temperature is 500-700°C, The roasting time...

Embodiment 1

[0034] Wet catalyst waste residue, obtained from Sinopec Catalyst Qilu Branch, has a solid content of 19.57% by weight, and the dry weight percentage is grouped as Na 2 O is 3.50%, MgO is 0.64%, Al 2 o 3 16.41%, SiO 2 36.96%, Re 2 o 3 6.00%, SO 3 18.13%, Fe 2 o 3 0.32%, K 2 O is 0.12%, Cl - 0.90%, CaO 14.20%, P 2 o 5 was 0.41%. The catalyst waste residue was dried at 150° C. for 2 hours, and 20 kg (dry basis) of the dried catalyst waste residue was taken with 100 kg deionized water and 4Kg NH 4 Cl mixed, adding hydrochloric acid to adjust the pH value to 3.0, beating at 60°C for 30min, filtering, washing the filter cake with 200Kg deionized water and roasting at 600°C for 1.5 hours, then the obtained roasted product was mixed with 100Kg deionized water and 2Kg NH 4 Mix with Cl, add hydrochloric acid to adjust the pH value to 3.0, beat at 60°C for 30 minutes, filter, wash the filter cake with 200Kg deionized water, and then dry at 140°C for 1.5 hours to obtain the ...

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Abstract

The invention discloses a method for utilizing residues of catalyst production, comprising the following steps: (1) drying catalyst residues; (2) contacting the material obtained by the step (1) with an ammonium salt solution or alkali metal saline solution to conduct ion exchange and washing, then filtering; (3) roasting the material obtained by the step (2) at 450-750 DEG C, then exchanging, washing and filtering; and (4) mixing the material obtained by the step (3) with molecular sieve residues and water and beating, filtering, drying, and then roasting at 500-700 DEG C to obtain an active carrier; and carrying out beating and spray drying on the active carrier, ultrastable Y-type molecular sieve, alumina binder and clay to obtain a cracking catalyst. The obtained catalytic cracking catalyst has the advantages of high cracking activity, high active stability, and low yields of dry gas and coke.

Description

technical field [0001] The invention relates to a utilization method of the waste residue produced in catalytic cracking catalyst production. Background technique [0002] The production of cracking catalysts usually includes synthesizing active components (usually molecular sieves), mixing and beating the active components and matrix, spray drying and molding, washing and other processes. During the production process, a large amount of wastewater will be generated, and the solids in the wastewater will settle, A large amount of solid waste was formed after filtration. [0003] The waste residue generated in the production of catalytic cracking catalyst can be divided into molecular sieve waste residue and catalyst waste residue. [0004] (1) Molecular sieve waste residue. Currently, the synthesis of active components of cracking catalysts usually includes the synthesis of molecular sieves and the modification of molecular sieves. The molecular sieve synthesis process is...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J32/00B01J29/90B01J29/16C10G11/05
Inventor 周健苗鹏杰
Owner CHINA PETROLEUM & CHEM CORP
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