Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Continuous reaction device and method for preparing aldehyde through hydroformylation reaction

A reaction device and chemical reaction technology, applied in the field of continuous reaction devices, can solve the problems of catalyst poisoning and deactivation, large energy consumption, and high energy consumption of the overall process

Active Publication Date: 2019-12-03
上海载正化工科技发展有限公司
View PDF4 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In order to maintain catalyst activity and high conversion rate, the process must adopt very high synthesis gas pressure and high temperature, and the positive and negative ratio of the obtained product is low, there are many side reactions, the overall process energy consumption is high, catalyst recovery and regeneration complicated process
BASF's process is similar to that of Ruhr in Germany, using a higher reaction temperature to increase the speed of the formylation reaction, but the side reactions increase more
Mitsubishi Chemical has improved the process, using automatic control and lower temperature (100-150 degrees) to make the temperature in the reactor uniform. Taking the production of butyraldehyde from propylene as an example, the selectivity can reach 85-88%. The ratio is 4:1; the disadvantage is that the reaction pressure is still high (15-30MPa), and the catalyst separation effect is complicated
The UCC process is jointly developed by the United Carbide Company of the United States, Davey Electric Company and Johnson Matthey Company of the United Kingdom. It uses a large amount of excess triphenylphosphine as a ligand and triphenylphosphine carbonyl rhodium hydride as a catalyst system, which can make the reaction at a relatively mild temperature. The operating pressure is greatly reduced. The disadvantage is that rhodium is expensive and the catalyst is poisoned and deactivated. This process is limited to low-carbon olefins as raw materials, and ethylene and propylene are used to produce propionaldehyde and butyraldehyde.
The core advantage of the RCH / RP process is the use of a special reactor. When the reaction product leaves the reactor, the separation process of the catalyst has been completed, and the catalyst remains in the reactor. However, the disadvantage is that the reaction temperature and pressure are relatively high. High, with a large amount of water circulation, high energy consumption

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Continuous reaction device and method for preparing aldehyde through hydroformylation reaction
  • Continuous reaction device and method for preparing aldehyde through hydroformylation reaction
  • Continuous reaction device and method for preparing aldehyde through hydroformylation reaction

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0122] use figure 1 As shown in the process flow, the process conditions are as follows:

[0123] The catalyst aqueous solution adopts the proportioning composition of Example 1 in the published patent number CN101462932A.

[0124] Reaction temperature: 80°C, reaction pressure is 2.5MPa (A);

[0125] Reactor inlet conditions:

[0126] Feed flow of catalyst aqueous solution: 10m 3 / Hour;

[0127] Ethylene feed flow: 25Nm 3 / Hour;

[0128] CO+H 2 Feed flow: 50Nm 3 / Hour;

[0129] CO:H 2 = 1:1 (molar ratio);

[0130] The discharge results at the discharge port 3:

[0131] Ethylene conversion rate: 98%;

[0132] Propionaldehyde yield: 98%.

[0133] In this example, the production process of preparing propionaldehyde by hydroformylation of ethylene olefin is realized with a high ethylene conversion rate of 98% and a high propionaldehyde selectivity of 98%.

Embodiment 2

[0135] use figure 1 As shown in the process flow, the process conditions are as follows:

[0136] The catalyst aqueous solution adopts the proportioning composition of Example 5 in the published patent number CN101462932A.

[0137] Reaction temperature: 110°C, reaction pressure 2.5MPa (A);

[0138] Reactor inlet conditions:

[0139] Feed flow of catalyst aqueous solution: 10m 3 / Hour;

[0140] Propylene feed flow: 50kg / hour;

[0141] CO+H 2 Feed flow: 50Nm 3 / Hour;

[0142] CO:H 2 = 1:1 (molar ratio);

[0143] The discharge results at the discharge port 3:

[0144] Propylene conversion rate: 98%;

[0145] n-Butyraldehyde yield: 97%;

[0146] n-Butyraldehyde:Isobutyraldehyde=40:1 (molar ratio).

[0147] In this example, the production process of preparing n-butyraldehyde by hydroformylation of propene olefin is realized with a high propylene conversion rate of 98% and a high n-butyraldehyde selectivity of 97%.

Embodiment 3

[0149] use figure 1 As shown in the process flow, the process conditions are as follows:

[0150] The catalyst aqueous solution adopts the proportioning composition of Example 10 in the published patent number CN101462932A.

[0151] Reaction temperature: 120°C, reaction pressure is 3.0MPa (A);

[0152] Reactor inlet conditions:

[0153] Feed flow of catalyst aqueous solution: 10m 3 / Hour;

[0154] 1-Butene feed flow: 60kg / hour;

[0155] CO+H 2 Feed flow: 50Nm 3 / Hour;

[0156] CO:H 2 = 1:1 (molar ratio);

[0157] The discharge results at the discharge port 3:

[0158] 1-Butene conversion rate: 97%;

[0159] n-valeraldehyde yield: 97%;

[0160] n-valeraldehyde:isovaleraldehyde = 60:1 (molar ratio).

[0161] In this example, the production process of preparing n-valeraldehyde by hydroformylation of 1-butene is realized with a high 1-butene conversion rate of 97% and a high n-valeraldehyde selectivity of 97%.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
pore sizeaaaaaaaaaa
diameteraaaaaaaaaa
lengthaaaaaaaaaa
Login to View More

Abstract

The invention discloses a continuous reaction device for preparing aldehyde through a hydroformylation reaction. The reaction device comprises a reaction unit, a separation unit and a circulation unit; the circulation unit is located between the reaction unit and the separation unit; the reaction unit is connected with the separation unit; and a catalyst is circulated between the reaction unit andthe separation unit through the circulation unit. The invention further discloses a method for preparing the aldehyde by adopting the reaction device. According to the method and device provided by the invention, the catalyst can be uninterruptedly and continuously recycled without being separated by external equipment, continuous production of the aldehyde can be realized, reaction heat can be rapidly removed, the progress of the hydroformylation reaction is facilitated, the conversion rate of raw materials is high, the yield of the target products is high, and the ratio of a n-configurationproduct to an iso-configuration product is high.

Description

Technical field [0001] The present application relates to a continuous reaction device for preparing aldehydes through hydroformylation reaction and a method for preparing aldehydes using the device, and belongs to the fields of chemical engineering and chemical synthesis. Background technique [0002] The hydroformylation reaction is a reaction between olefins and synthesis gas (CO and H 2 ) is a reaction process that produces one molecule more aldehyde or alcohol than the original olefin under the action of a transition metal complex catalyst. The aldehydes, alcohols, and their derivatives produced are widely used as plasticizers, fabric additives, surfactants, solvents, and fragrances. This type of reaction was first discovered by O. Roelen in Fischer-Tropsch synthesis at the Ruhr Chemical Company in Germany in 1938. Propanaldehyde and ethylenedione were obtained from synthesis gas and ethylene, and were soon applied to propylene. Process for producing butanol. However...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07C45/50C07C47/02
CPCC07C45/50C07C47/02B01J10/00C07C45/59Y02P20/584
Inventor 安丽华
Owner 上海载正化工科技发展有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products