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Method for preparing isoamylene from methyl tert-amyl ether

A technology for methyl tert-amyl ether and isopentene, applied in the field of preparing isopentene, can solve the problems of reduced product yield, abnormal fluctuation of catalyst bed temperature, increased energy consumption, etc., and achieves improved conversion rate and selectivity , Eliminate the abnormal fluctuation of bed temperature and reduce the effect of content

Inactive Publication Date: 2009-12-09
SINOPEC SHANGHAI PETROCHEMICAL CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] However, while the isomerization reaction is carried out, 2-methyl-2-butene and 2-methyl-1-butene are all prone to dimerization reactions individually or with each other. Dimer content will reach about 4wt%
Although the dimer can be removed through the refining process, this will lead to a decrease in product yield and an increase in energy consumption
On the other hand, the reaction heat of the dimerization reaction will also cause abnormal fluctuations in the temperature of the catalyst bed, making it difficult to control the isomerization reaction smoothly.

Method used

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  • Method for preparing isoamylene from methyl tert-amyl ether
  • Method for preparing isoamylene from methyl tert-amyl ether

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1~10

[0023] 1. Thermal cracking of methyl tert-amyl ether

[0024] The raw material for the reaction is the methyl tert-amyl ether obtained by reacting the by-product C5 fraction produced by steam cracking of naphtha to ethylene and methanol. After methyl tert-amyl ether is heated and vaporized, the α-Al is modified by HF in the gas phase. 2 o 3 The packed catalyst bed carries out etherolysis reaction, and the reaction temperature is controlled at 180-230°C. The etherolysis reaction product was washed with water to remove methanol to obtain crude isopentene, whose components are shown in Table 1.

[0025] Table 1.

[0026] 2MB2

(wt%)

2MB1

(wt%)

2MB2 / 2MB1

(mass ratio)

TAME

(wt%)

Isoprene dimer

(wt%)

Other carbon five and other impurities

74.18

25.04

2.96

0.57

0.04

margin

[0027] 2. Isomerization reaction

[0028] The isomerization reaction is carried out in a stainless ...

Embodiment 3

[0039] The isomerization reaction product obtained in Example 3 is further subjected to rectification and purification, and refined isopentene is produced in the side stream, and light components and heavy components of impurities are discharged from the top of the tower and the bottom of the tower respectively. The specific rectification conditions are shown in Table 4, and the refined isopentene product is analyzed by chromatographic analysis, and the main indicators are shown in Table 5.

[0040] Table 4.

[0041] Tower kettle temperature

(℃)

Top temperature

(℃)

operating pressure

(MPa)

Reflux ratio

Example 11

125

68

0.50

3.0

Example 12

120

64

0.15

2.0

Example 13

123

65

0.30

3.0

Example 14

115

59

0.10

1.0

[0042] table 5.

[0043] 2MB2 content

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Abstract

The invention relates to a method for preparing isoamylene from methyl tert-amyl ether, which comprises the following steps: (1) methyl tert-amyl ether is subjected to an ether analysis reaction through a catalyst bed layer in a gas phase at 130-300 DEG C; (2) methanol in a product of the ether analysis reaction is removed so as to obtain a coarse isoamylene material; (3) tert butyl alcohol is added to the coarse isoamylene material, and then an isomerization reaction is carried out through the catalyst bed layer in a liquid phase so as to ensure that 2-methyl-1-butylene in the coarse isoamylene is converted into 2-methyl-2-butylene, wherein the addition of the tert butyl alcohol takes the coarse isoamylene as a reference and is 0.2-2.2 percent by weight; the mass space velocity is 1-35 hr, and the reaction temperature is 18-45 DEG C; and the reaction pressure is 0.3-1.0 MPa. Sulfonic acid group cationic exchange resin is used as a catalyst, and the mass exchange capacity of the catalyst is 3-5.5 mmol / g. The method effectively restrains respective or mutual dipolymer reactions of the 2-methyl-2-butylene and the 2-methyl-1-butylene in the process of the isomerization reaction.

Description

technical field [0001] The present invention relates to a method for preparing isopentene from methyl tert-amyl ether, in particular to crude isopentene obtained by etherolysis for further isomerization reaction through a fixed-bed catalyst bed composed of sulfonic acid-based cation exchange resin , to improve the method for preparing isopentene of which 2-methyl-2-butene content. Background technique [0002] Isoamylene is an important chemical raw material used in the production of resins and pesticide intermediates. Isoamyl is usually a mixture of 2-methyl-2-butene and 2-methyl-1-butene. Since only 2-methyl-2-butene is the active ingredient for most reactions, isoamyl The higher the 2-methyl-2-butene content, the higher the application value. [0003] Isoamylene mainly exists in the C5 fraction of catalytic cracked gasoline or the C5 fraction of the by-product of naphtha cracking to ethylene. Since these C5 materials contain many compounds with very close boiling points...

Claims

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Application Information

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IPC IPC(8): C07C1/20C07C11/10
Inventor 唐豪孙春水毛斌孙骏叶军明瞿卫国
Owner SINOPEC SHANGHAI PETROCHEMICAL CO LTD
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