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Catalyst for preparing isoamylene by splitting decomposition of t-amyl-methyl ether and preparation method and application thereof

A technology of methyl tert-amyl ether and isopentene, which is applied in chemical instruments and methods, hydroxyl compound preparation, physical/chemical process catalysts, etc., can solve the problem of high energy consumption, low conversion rate and low space velocity of ether hydrolysis And other issues

Active Publication Date: 2013-04-17
EAST CHINA UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But the temperature is high, and some side reactions will also occur, such as the loss of isopentene caused by the oligomerization of isopentene; the methanol obtained by cracking is dehydrated to generate dimethyl ether, and the production of dimethyl ether will reduce the recovery rate of methanol, resulting in the need to regenerate Add a large amount of methanol to the initial etherification reaction system; the water produced during the formation of dimethyl ether and the hydration of isopentene also cause the loss of the product, and the generation of by-product tert-amyl alcohol increases the cost of the separation and purification of the product, etc.
The disadvantage of ion exchange resin catalysts is poor high temperature resistance. When the reaction temperature is too high, the active components in it are easy to decompose and fall off. Due to the limitation of the reaction temperature, the conversion rate of the reaction is low.
The disadvantages of heteropoly acid system catalysts are low space velocity for etherolysis reaction, low production efficiency, relatively high reaction temperature, and high energy consumption
The conversion rate of TAME by fluoride system catalyst is relatively low

Method used

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  • Catalyst for preparing isoamylene by splitting decomposition of t-amyl-methyl ether and preparation method and application thereof
  • Catalyst for preparing isoamylene by splitting decomposition of t-amyl-methyl ether and preparation method and application thereof
  • Catalyst for preparing isoamylene by splitting decomposition of t-amyl-methyl ether and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030]30 g γ-Al 2 o 3 Add it to 50ml of 20% phosphoric acid solution and let stand at room temperature for 1h, then filter, dry at 90°C for 4h, and roast at 800°C for 4h to obtain PO 4 = / Al 2 o 3 .

[0031] The product was then dissolved in 40ml of 18% La(NO 3 ) 3 In aqueous solution, soak for 6 hours, filter, dry at 100°C for 8 hours, and roast at 800°C for 8 hours to obtain La 2 o 3 / PO 4 = / Al 2 o 3 .

[0032] La 2 o 3 / PO 4 = / Al 2 o 3 Add it into 50ml of 20% ammonium fluoride solution, filter, dry at 100°C for 4h, and roast at 800°C for 5h to obtain F / La of the present invention 2 o 3 / PO 4 = / Al 2 o 3 .

[0033] Put 14g of catalyst into a miniature fixed-bed reactor with a diameter of Φ20mm, feed methyl tert-amyl ether with a liquid micro-sampling pump, and control the liquid space velocity to 2h -1 , the reaction temperature is 170°C, the conversion rate of TAME is 99.4%, the selectivity of isoamylene is 100%, and the selectivity of methanol i...

Embodiment 2

[0035] 30 g γ-Al 2 o 3 Add it to 50ml of 46% ammonium bisulfate solution and let stand at room temperature for 8h, then filter, dry at 100°C for 4h, and roast at 800°C for 3h to obtain SO 4 = / Al 2 o 3 .

[0036] The product was then dissolved in 40ml of 0.5% Ce(NO 3 ) 3 In aqueous solution, soak for 2h, filter, dry at 150°C for 1h, and calcinate at 800°C for 4h to obtain Ce 2 o 3 / SO 4 = / Al 2 o 3 .

[0037] Then Ce 2 o 3 / SO 4 = / Al 2 o 3 Add it to 50ml of 30% sodium fluoride solution, filter, dry at 120°C for 5h, and roast at 800°C for 5h to obtain the F / Ce of the present invention 2 o 3 / SO 4 = / Al 2 o 3 .

[0038] Put 14g of catalyst into a miniature fixed-bed reactor with a diameter of Φ20mm, feed methyl tert-amyl ether with a liquid micro-sampling pump, and control the liquid space velocity to 3h -1 , the reaction temperature is 160°C, the conversion rate of TAME is 99.6%, the selectivity of isoamylene is 100%, and the selectivity of methanol i...

Embodiment 3

[0040] 30 g γ-Al 2 o 3 Add it to 50ml of 0.5% ammonium phosphate solution and let stand at room temperature for 6h, then filter, dry at 100°C for 8h, and roast at 300°C for 8h to obtain PO 4 = / Al 2 o 3 .

[0041] The product was then dissolved in 40ml of 10% Sm(NO 3 ) 3 Soak in aqueous solution for 6h, filter, dry at 100°C for 4h, and roast at 800°C for 1h to obtain Sm 2 o 3 / PO 4 = / Al 2 o 3 .

[0042] Sm again 2 o 3 / PO 4 = / Al 2 o 3 Add it to 50ml of 40% hydrofluoric acid solution and soak for 1h, filter, dry at 100°C for 4h, and roast at 800°C for 5h to obtain the F / Sm of the present invention 2 o 3 / PO 4 = / Al 2 o 3 .

[0043] Put 14g of catalyst into a miniature fixed-bed reactor with a diameter of Φ20mm, feed methyl tert-amyl ether with a liquid micro-sampling pump, and control the liquid space velocity to 2h -1 , the reaction temperature is 170°C, the conversion rate of TAME is 99.1%, the selectivity of isoamylene is 100%, and the selectivity...

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Abstract

The invention discloses a multicomponent (X / Z2O3 / YO4 / Al2O3) catalyst for preparing isoamylene and a preparation method thereof. According to the method, the catalyst comprises the following components by weight percent: 20% to 95% of Al2O3, 0.1% to 20% of Z2O3, 0.1% to 50% of YO4 and 0.1% to 40% of X. The catalyst can take a reaction to prepare the isoamylene by the splitting decomposition of t-amyl-methyl ethe at a temperature lower than that of the existing catalyst of the same type. Under the condition that the high selection on the isobutene and the methanol and the high conversion rate of the splitting decomposition of the t-amyl-methyl ether are guaranteed, as compared with the existing catalyst of the same type, the catalyst provided by the invention has the effects that the space velocity of liquids in the reaction is improved exponentially, and water and other inert substances are not required to be added into a splitting decomposition reaction system of the t-amyl-methyl ether. Therefore, under the condition of unchanging the existing reaction equipment, the energy consumption in the industrial production is lowered, and the equipment utilization rate is improved exponentially.

Description

technical field [0001] The invention relates to the preparation and application of a catalyst for preparing isopentene by cracking methyl tert-amyl ether (TAME). Mainly concerned with rare earth oxides, YO 4 = and multi-component X / Z with halogen supported on Al2O3 2 o 3 / YO 4 = / Al 2 o 3 type catalyst. Background technique [0002] Isoamyl is a mixture of 2-methyl-2-butene and 2-methyl-1-butene, and 2-methyl-2-butene is the active ingredient in most reactions, so 2-methyl-2 - The higher the butene content, the higher the value contained. As an important chemical raw material, isobutylene is widely used in the production of isoprene, pinacolone (methyl tert-butyl ketone), tert-amyl alcohol, spices and pesticides, and can also be used as an intermediate for synthetic rubber and resin, among which For the production of pesticides and spices accounted for the vast majority. Especially with the prohibition of phosphorus-containing pesticides in China, isopentene has b...

Claims

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Application Information

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IPC IPC(8): B01J27/18B01J27/125C07C11/10C07C1/20C07C31/04C07C29/00
CPCY02P20/52
Inventor 王筠松陆文龙卢冠忠郭杨龙詹望成郭耘王艳芹
Owner EAST CHINA UNIV OF SCI & TECH
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