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Alumina preparation method

A technology of alumina and aluminum sulfate, applied in the preparation of alumina/hydroxide, etc., can solve the problems of long production process, high preparation cost, small specific surface area, etc., and achieves short process, simple and easy operation steps, and improved properties. Effect

Active Publication Date: 2020-09-11
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the invention is simple and feasible, electrolytic alumina can be successfully prepared, but the specific surface area of ​​this alumina is too small to meet the demand for large specific surface area of ​​catalytic alumina in the chemical industry
[0008] In summary, although the existing methods for preparing alumina are various and very mature, they all have long production processes, complicated operation steps, high preparation costs, and the properties of the prepared alumina products cannot meet the needs of the chemical industry. The problem of the demand for large specific surface area of ​​alumina for catalysis

Method used

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Experimental program
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Effect test

Embodiment 1

[0030] (1) Mix 10g of aluminum sulfate, 0.25g of ferric nitrate, and 100mL of distilled water evenly, then place in a 70°C water bath and stir until the solution becomes viscous; then dry at 120°C for 10 hours.

[0031] (2) Put the substance obtained in the previous step in a closed reactor, and feed hydrogen gas at a flow rate of 400mL / min; heat up to 300°C at 5°C / min for 2 hours; then heat up to 600°C at 5°C / min for 3 hours .

[0032] (3) Mix the substance obtained in the previous step with 5L hydrochloric acid (8%) and treat it at 25°C for 2h, then wash with distilled water until neutral, and dry at 120°C for 10h to obtain the alumina product. The obtained sample number is CL1, and the crystal phase structure is shown in figure 1 , the pore size distribution see figure 2 , and other properties are shown in Table 1. From figure 1 , figure 2 It can be seen from Table 1 that the obtained sample is γ-alumina with good pore structure.

Embodiment 2

[0034] (1) Mix 15g of aluminum sulfate, 0.25g of ferric nitrate, and 100mL of distilled water evenly, then place in a 75°C water bath and stir until the solution becomes viscous; then dry at 120°C for 10 hours.

[0035] (2) Put the substance obtained in the previous step in a closed reactor, and feed hydrogen gas at a flow rate of 500mL / min; heat up to 320°C at 8°C / min for 2 hours; then heat up to 650°C at 8°C / min for 4 hours .

[0036] (3) Mix the substance obtained in the previous step with 5.5L hydrochloric acid (8%) and treat it at 25°C for 3 hours, then wash it with distilled water until it becomes neutral, and dry it at 120°C for 10 hours to obtain the alumina product. The obtained sample number is CL2, and the obtained sample is γ-alumina with good pore structure.

Embodiment 3

[0038] (1) Mix 20g of aluminum sulfate, 0.3g of ferric nitrate, and 150mL of distilled water evenly, then place them in a water bath at 85°C and stir until the solution becomes viscous; then dry at 120°C for 10 hours.

[0039] (2) Put the substance obtained in the previous step in a closed reactor, and feed hydrogen gas at a flow rate of 500mL / min; heat up to 320°C at 11°C / min for 2 hours; then heat up to 550°C at 11°C / min for 4.5 h.

[0040] (3) Mix the substance obtained in the previous step with 4L hydrochloric acid (7%) and treat it at 25°C for 2h, then wash with distilled water until neutral, and dry at 120°C for 10h to obtain the alumina product. The obtained sample number is CL3, and the obtained sample is γ-alumina with good pore structure.

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Abstract

The invention provides a method for preparing aluminum oxide. The aluminum oxide is crystalline aluminum oxide and belongs to gamma-aluminum oxide in crystal structure, and the aluminum oxide has thesurface area of 150-400 m<2> / g and the pore volume of 0.2-0.55 cm<3> / g; the aluminum oxide has centralized pore size distribution. The preparation method comprises steps as follows: ferric nitrate, aluminum sulfate and water are mixed until full dissolution, then, stirring treatment is performed until the solution becomes a viscous state, and then, drying treatment is performed; an obtained substance is put in a reactor, hydrogen is introduced, and the mixture is heated with a certain heating procedure to a set temperature and treated at the constant temperature for a period of time; the obtained substance and hydrochloric acid are mixed for treatment, the mixture is washed to be neutral and then dried, and an aluminum oxide product is obtained. The provided preparation method is simple and easy to implement and low in production cost.

Description

technical field [0001] The invention relates to a method for preparing alumina, in particular to a method for preparing alumina with aluminum sulfate. Background technique [0002] Activated alumina is an important industrial catalyst carrier due to its porosity, high dispersion, large specific surface area and thermal stability. There are many ways to prepare activated alumina, two of which are more common, one is the Bayer process, that is, heating and dehydrating gibbsite or industrial aluminum hydroxide at high temperature; the other is by neutralizing solutions such as aluminum salts or by alcohol Aluminum is decomposed to obtain aluminum glue, and then activated at high temperature to prepare activated alumina. [0003] CN02158286.6 discloses a preparation method of activated alumina, which is a sodium metaaluminate solution prepared by aluminum hydroxide powder and sodium hydroxide, and the CO 2 Gel; then dry, and bake at 500 ~ 700 ℃ to get activated alumina. [00...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01F7/32
CPCC01F7/32C01P2002/72C01P2006/12C01P2006/14C01P2006/17
Inventor 孙晓彤范峰凌凤香张会成王少军杨春雁
Owner CHINA PETROLEUM & CHEM CORP