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Method for preparation of dimethyl ether

A technology of catalyst and dimethyl ether, which is applied in the field of preparation of dimethyl ether catalyst, can solve the problems of low catalyst performance, high reaction temperature, poor catalyst repeatability, etc., and achieve high activity, stability and high activity effect

Active Publication Date: 2011-07-20
CHNA ENERGY INVESTMENT CORP LTD +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, in the above patents, the reaction temperature is above 250°C
[0004] In the prior art, in the catalyst prepared by mechanical mixing, the contact between the two components is not close enough, the synergistic effect is poor, and the catalyst performance is low; the catalyst prepared by impregnation and co-deposition method, due to the influence of co-deposition method on temperature, acid-base, etc. There are strict requirements on the temperature and drop rate of the solution, and the particle size of the methanol dehydration catalyst also has strict requirements. After deposition, the catalyst needs to be fully washed, the preparation process is relatively complicated, and the repeatability of each batch of catalysts is relatively poor, which cannot meet the needs of industrial production. ; and the reaction temperature is high, the methanol synthesis catalyst component and the methanol dehydration catalyst component cannot be in the optimum condition at the same time

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] 2% lanthanum nitrate (purchased from Tianjin Damao Chemical Reagent Factory) aqueous solution 200g and 200g gamma-alumina (Dalian Ruike Technology Co., Ltd.) powder were kneaded and extruded, then roasted at 550°C for 5 hours, cooled, and pulverized to The lanthanum oxide accounts for 1% of the modified γ-alumina for use below 100 mesh. Add 150g of water into the colloid mill (purchased from Dalian Xinghuo Packaging Machinery Factory, model is JM-50), start the colloid mill, then add the above-mentioned modified γ-alumina 30g, grind for 4 hours, and take the methanol synthesis catalyst component ( Dalian Ruike Technology Co., Ltd.) 60g (on a dry basis), aluminum glue (Dalian Ruike Technology Co., Ltd.) 3g (on a dry basis) were added to the colloid mill, and continued to grind for 2 hours; wherein the methanol synthesis catalyst group It is the intermediate product carbonate mixture of copper-zinc-aluminum methanol synthesis catalyst, which contains basic copper carbonat...

Embodiment 2

[0022] The method and steps of catalyst preparation are as in Example 1, except that 1% lanthanum nitrate and 1% cerium nitrate (purchased from Tianjin Damao Chemical Reagent Factory) mixed aqueous solution is used to knead gamma-alumina, the grinding time is 8 hours, and the colloid The particle size of each component in the method is below 3 microns, and the dimethyl ether catalyst is obtained by drying, roasting and pulverizing as well. The ratio of methanol synthesis catalyst component to methanol dehydration catalyst component is 2:1, and the specific surface area of ​​the prepared catalyst is 158.45m 2 / g, the pore volume is 0.3528cc / g, and the catalyst activity evaluation results are shown in Table 2.

Embodiment 3

[0024] The method and steps of catalyst preparation are as in Example 2. After adding modified gamma-alumina, the grinding time is 8 hours, and 150 g (in dry basis) of the intermediate colloidal carbonate mixture of copper-zinc-aluminum methanol synthesis catalyst is added, The substance contains basic copper carbonate, basic zinc carbonate and aluminum oxide, and after roasting at 500°C, the weight contents of copper oxide, zinc oxide and aluminum oxide are 55.43%, 24.63% and 8.84% respectively. After grinding, it is measured that the particle size of each component in the colloid is below 3 microns, and the dimethyl ether catalyst is also obtained by drying, roasting and pulverizing. The ratio of the methanol synthesis catalyst component to the methanol dehydration catalyst component is 5:1, and the catalyst activity evaluation results are shown in Table 3.

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Abstract

The invention relates to a method for the preparation of dimethyl ether, which comprises the steps of: using the intermediate product of a copper-zinc-aluminum methanol synthesis catalyst, i.e. the carbonate mixture, as the component of the methanol synthesis catalyst, using rare earth modified gamma-alumina with low temperature activity as the component of the methanol synthesis catalyst, sufficiently mixing the two components according to the method based on colloidal sedimentation and mechanical mixing, and activating the mixture to obtain dimethyl ether. The method of the invention is simple in process and ensures the repeatability in catalyst preparation; the catalyst prepared according to the method has small particle size and high specific surface area; and the catalyst has high activity owing to tight contact and strong synergistic effect between the components.

Description

technical field [0001] The present invention relates to a kind of catalyst preparation method, more specifically, relate to a kind of preparation method of dimethyl ether catalyst. Background technique [0002] Dimethyl ether is a chemical product with a wide range of uses, and it has many unique functions in pharmaceuticals, pesticides, fuels, and daily chemical products. Traditional uses include replacing halogenated hydrocarbons in propellants, environmentally friendly refrigerants, and aerosols. Studies in recent years have shown that DME can also be directly used as fuel as a substitute for liquefied petroleum gas and diesel. With the development of the coal-to-olefins industry, DME can also be used as an important raw material for the production of low-carbon olefins. Therefore, the potential market of DME is very huge. [0003] The original process of methanol dehydration to dimethyl ether is mature. In recent years, a lot of research has been done on catalysts fo...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/83C07C43/04C07C41/01
Inventor 周焕文姚敏邓少亮乔川曲雪琴焦洪桥艾玉廉潘强颜蜀雋任立军宋彩霞
Owner CHNA ENERGY INVESTMENT CORP LTD
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