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Preparation method of aluminum oxide

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

Active Publication Date: 2018-06-01
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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  • Preparation method of aluminum oxide
  • Preparation method of aluminum oxide
  • Preparation method of aluminum oxide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

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

[0031] (2) The material obtained in the previous step was placed in a closed reactor, and hydrogen was introduced at a flow rate of 400 mL / min; the temperature was raised to 300 °C at a constant temperature of 5 °C / min for 2 h; .

[0032] (3) The material obtained in the previous step was mixed with 5L hydrochloric acid (8%) and treated at 25°C for 2h, then washed with distilled water until neutral, and dried at 120°C for 10h to obtain alumina product. The obtained sample number CL1, see the crystal phase structure figure 1 , see pore size distribution 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 and has a good pore structure.

Embodiment 2

[0034] (1) Mix 15g aluminum sulfate, 0.25g ferric nitrate, and 100mL 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) The material obtained in the previous step was placed in a closed reactor, and hydrogen was introduced at a flow rate of 500 mL / min; the temperature was heated to 320 °C at 8 °C / min for 2 h; and then heated to 650 °C at 8 °C / min for 4 h. .

[0036] (3) The substance obtained in the previous step was mixed with 5.5L hydrochloric acid (8%) and treated at 25°C for 3h, then washed with distilled water until neutral, and dried at 120°C for 10h to obtain 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 it in a water bath at 85°C and stir until the solution becomes viscous; then dry at 120°C for 10 hours.

[0039] (2) The material obtained in the previous step was placed in a closed reactor, and hydrogen was introduced at a flow rate of 500 mL / min; the temperature was raised to 320°C at 11°C / min for 2 h; and then the temperature was raised to 550°C at 11°C / min for 4.5 h.

[0040] (3) The material obtained in the previous step was mixed with 4L hydrochloric acid (7%), treated at 25°C for 2h, washed with distilled water until neutral, and dried at 120°C for 10h to obtain 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 dispersibility, large specific surface area and thermal stability. There are many preparation methods of activated alumina, two of which are more common, one is the Bayer method, that is, gibbsite or industrial aluminum hydroxide is heated and dehydrated 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 CO 2 Gel; then dry, and calcined at 500 ~ 700 ℃ to obtain activated ...

Claims

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Application Information

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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