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A kind of method of low carbon alkane dehydrogenation reaction

A technology for the dehydrogenation of low-carbon alkanes, which is applied in the direction of hydrocarbons, hydrocarbons, chemical instruments and methods, etc., can solve problems such as complex processes, high sulfur concentration, and heat treatment of catalysts, so as to improve the selectivity of olefins and improve Activity stability, simple and safe effect

Active Publication Date: 2021-02-09
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] The start-up method of the above dehydrogenation catalyst or the treatment method before use is relatively complicated. The sulfur-containing solution is dangerous in the process of configuration and use, and the sulfur concentration is very high during sulfidation. The sulfided catalyst needs heat treatment.

Method used

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  • A kind of method of low carbon alkane dehydrogenation reaction
  • A kind of method of low carbon alkane dehydrogenation reaction

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Get a spherical Sn-containing θ-alumina carrier (produced by Sasol, Germany), the Sn content is 0.30% by mass of the carrier mass, impregnate at 25°C for 4 hours with an impregnating solution containing chloroplatinic acid and hydrochloric acid, and the impregnating solution contains 0.30% by mass % of platinum, 1.5% by mass of chlorine (all relative to the mass of alumina on a dry basis, the same below), and the liquid / solid ratio is 1.8mL / g. After impregnation, the solid was dried at 120°C for 12 hours and calcined at 500°C for 4h. The calcined solid was impregnated with potassium hydroxide solution at 25° C. for 4 hours, the solution contained 1.0% by mass of potassium (relative to the mass of alumina on a dry basis), and the liquid / solid ratio was 1.4 mL / g. After impregnation the solid was dried at 120°C for 12 hours. Afterwards, the catalyst was subjected to oxychlorination treatment with air containing water and HCl at 550°C for 4 hours. During the oxychlorinatio...

Embodiment 2

[0038] The dehydrogenation catalyst was prepared in the same manner as in Example 1.

[0039] Put the above-mentioned catalyst into the dehydrogenation reactor, blow and replace it with nitrogen, then raise the temperature from room temperature to 450°C under a nitrogen atmosphere, then stop feeding nitrogen, and feed hydrogen containing hydrogen sulfide, wherein the volume concentration of hydrogen sulfide is 100ppm, and then heated up to 580°C for sulfidation treatment for 2 hours, and the treated catalyst was designated as B. Then feed propane, heat up to 620° C. for dehydrogenation reaction, and continuously feed the hydrogen gas containing hydrogen sulfide during the dehydrogenation reaction, and the reaction conditions are the same as in Example 1. After reacting for 50 hours, the propane conversion rate and propylene selectivity were calculated, and the results are shown in Table 1.

Embodiment 3

[0041] The dehydrogenation catalyst was prepared in the same manner as in Example 1.

[0042] Put the above-mentioned catalyst into the dehydrogenation reactor, blow and replace it with nitrogen, then raise the temperature from room temperature to 450°C under the hydrogen atmosphere, and feed the hydrogen containing hydrogen sulfide, wherein the volume concentration of hydrogen sulfide is 200ppm, and then raise the temperature to 620 ℃ for 4h, and the treated catalyst is denoted as C. Pass into propane to carry out dehydrogenation reaction afterwards, and in the process of dehydrogenation reaction, continue to pass into described hydrogen containing hydrogen sulfide, reaction condition is identical with embodiment 1. After reacting for 50 hours, the propane conversion rate and propylene selectivity were calculated, and the results are shown in Table 1.

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Abstract

The invention relates to the field of production of olefins through light alkane dehydrogenation and discloses a method for light alkane dehydrogenation reaction. The method comprises the following steps: filling a dehydrogenation reactor with a light alkane dehydrogenation catalyst, raising the temperature to 300-450 DEG C in a hydrogen or nitrogen atmosphere, introducing hydrogen containing hydrogen sulfide, and performing sulfurizing treatment at the temperature of 500-620 DEG C; and introducing light alkane, and carrying out dehydrogenation reaction at the temperature of 580-650 DEG C; andcontinuously introducing the hydrogen containing hydrogen sulfide in the dehydrogenation reaction process, wherein the volume concentration of the hydrogen sulfide in the hydrogen containing hydrogensulfide is 20-500ppm. According to the method disclosed by the invention, high light alkane dehydrogenation activity, olefin selectivity and activity stability can be obtained.

Description

technical field [0001] The invention relates to the field of dehydrogenation of low-carbon alkanes to olefins, in particular to a method for the dehydrogenation of low-carbon alkanes. Background technique [0002] With the increase of crude oil processing in our country, a large amount of low-carbon alkanes such as ethane, propane, and isobutane will be by-produced in the catalytic cracking process of the refinery. How to effectively utilize these resources and convert them into low-carbon olefins with high added value is of great significance to improve the economic benefits of refineries. [0003] Propylene is an important basic organic chemical raw material, widely used in the production of polypropylene, acetone, acrylonitrile, propylene oxide, acrylic acid and other chemical products; isobutylene is the main raw material for the production of methyl tert-butyl ether (MTBE); Butene is mainly used in alkylation, superposition, isomerization and dimerization processes to ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C11/06C07C5/333B01J37/20B01J27/135
CPCB01J27/135B01J37/20C07C5/333C07C5/3332C07C2521/04C07C2527/135C07C11/06Y02P20/52
Inventor 刘昌呈王春明马爱增
Owner CHINA PETROLEUM & CHEM CORP