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A kind of isobutylene catalyst from methyl bromide treated by alcohol solution and its preparation method and application

A catalyst, a technology for methyl bromide, applied in the field of high-selectivity methyl bromide catalyst for isobutene production and the preparation thereof, can solve the problems of low selectivity of a single product, high selectivity synthesis of isobutylene from methyl bromide and the like, and achieve a simple preparation method and mild reaction conditions. , the effect of high product selectivity

Active Publication Date: 2018-08-14
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In the technology with higher value-added low-carbon olefins as the target product, the selectivity of a single product is not high, and no relevant reports have been found on the synthesis of isobutene with high selectivity from methyl bromide

Method used

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  • A kind of isobutylene catalyst from methyl bromide treated by alcohol solution and its preparation method and application

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Weigh an appropriate amount of zinc nitrate and dissolve it in deionized water, and load it on a silica carrier (the pore volume is 1.06ml / g, the specific surface area is 387m 2 / g, spherical shape, equivalent diameter 0.5mm), dried at 100°C for 6h, and calcined at 500°C for 6h to obtain the catalyst precursor ZnO / SiO 2 . Prepare 2mol / L methanol aqueous solution, according to the solution and ZnO / SiO 2 The mixture was mixed at a weight ratio of 15, placed in a heating reflux apparatus, the temperature was controlled at 60°C, and heated to reflux for 2 hours. After cooling down, the solid and liquid were separated, and the obtained solid was dried at 90°C for 2 hours. Then the dried solid was placed in a continuous flow fixed bed reactor, and the catalyst precursor was treated with a mixed gas of methyl bromide and nitrogen. The volume concentration of methyl bromide was 80%, and the treatment conditions were 250°C, 0.2MPa (absolute pressure), 300h -1 , Time 2h, prepar...

Embodiment 2

[0033] Weigh an appropriate amount of zinc nitrate and dissolve it in deionized water, and load it on a silica carrier (the pore volume is 1.06ml / g, the specific surface area is 387m 2 / g, spherical shape, equivalent diameter 0.5mm), dried at 100°C for 6h, and calcined at 500°C for 6h to obtain the catalyst precursor ZnO / SiO 2 . Prepare 1mol / L methanol aqueous solution, according to the solution and ZnO / SiO 2 The mixture was mixed at a weight ratio of 15, placed in a heating reflux apparatus, the temperature was controlled at 60°C, and heated to reflux for 2 hours. After cooling down, the solid and liquid were separated, and the obtained solid was dried at 90°C for 2 hours. Then the dried solid was placed in a continuous flow fixed bed reactor, and the catalyst precursor was treated with a mixed gas of methyl bromide and nitrogen. The volume concentration of methyl bromide was 80%, and the treatment conditions were 250°C, 0.2MPa (absolute pressure), 300h -1 , Time 2h, prepar...

Embodiment 3

[0037] Weigh an appropriate amount of zinc nitrate and dissolve it in deionized water, and load it on a silica carrier (the pore volume is 1.06ml / g, the specific surface area is 387m 2 / g, spherical shape, equivalent diameter 0.5mm), dried at 100°C for 6h, and calcined at 500°C for 6h to obtain the catalyst precursor ZnO / SiO 2 . Prepare 3mol / L methanol aqueous solution, according to the solution and ZnO / SiO 2 The mixture was mixed at a weight ratio of 15, placed in a heating reflux apparatus, the temperature was controlled at 60°C, and heated to reflux for 2 hours. After cooling down, the solid and liquid were separated, and the obtained solid was dried at 90°C for 2 hours. Then the dried solid was placed in a continuous flow fixed bed reactor, and the catalyst precursor was treated with a mixed gas of methyl bromide and nitrogen. The volume concentration of methyl bromide was 80%, and the treatment conditions were 250°C, 0.2MPa (absolute pressure), 300h -1 , Time 2h, prepar...

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Abstract

The invention discloses an isobutene catalyst prepared from alcohol solution treated methyl bromide and a preparation method and application of the isobutene catalyst. The preparation method comprises the following steps that firstly, zinc oxide or zinc oxide and zirconia are introduced into a silicon dioxide carrier; secondly, the material obtained in the first step is treated through an alcohol water solution; thirdly, the catalyst precursor obtained in the second step is subjected to bromination treatment, the content, by weight, of the zinc oxide in the prepared catalyst is 0.5-20%, and the content, by weight, of zinc bromide is 10-50%. The catalyst can remarkably improve the selectivity of isobutene.

Description

technical field [0001] The invention relates to a catalyst for preparing isobutylene from methyl bromide, a preparation method and application thereof, in particular to a catalyst for preparing isobutene with high selectivity from methyl bromide treated with an aqueous alcohol solution, and a preparation method and application thereof. Background technique [0002] Isobutene is an important basic organic chemical raw material. Its derivative products are numerous, the upstream and downstream industrial chains are complicated, and the consumption structure shows a trend of diversification. A variety of high value-added products can be prepared from isobutylene, such as: butyl rubber, polyisobutylene, methyl tert-butyl ether, isoprene and organic glass and other organic chemical raw materials and fine chemical products. As the market scale of isobutene downstream products continues to expand, the contradiction between supply and demand will gradually become prominent, especial...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/138C07C1/26C07C11/09
CPCY02P30/20Y02P30/40
Inventor 张舒冬张信伟孙晓丹李杰倪向前张喜文刘继华
Owner CHINA PETROLEUM & CHEM CORP