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

Method for preparing diisopropanolamine

A technology of diisopropanolamine and temperature control, applied in chemical instruments and methods, preparation of organic compounds, preparation of aminohydroxy compounds, etc., can solve the problems of high isomer content, inability to synthesize intermediates and the like, Achieve the effect of high product quality, low production cost and low production operation cost

Active Publication Date: 2008-09-17
NANJING BAOCHUN CHEMICAL INDUSTRY CO LTD
View PDF0 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The technical problem to be solved by the present invention is the problem that the isomer content in the 1,1'-azonylidene dipropan-2-ol synthesized by the existing method is relatively high and cannot be used in the synthesis intermediate of medicine or pesticide , to provide a new synthesis of 1,1'-azinoalkyldipropan-2-ol, which can directly control the isomers within 1% in the synthesis stage, so that the product 1,1'- Azadipropan-2-ol can meet the high-end needs of synthetic medicine, pesticide and other products

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0015] Fully mix 4950kg liquid ammonia and 50kg deionized water to form ammonia water (water 1%), transport it with a high-pressure metering pump, and then use another high-pressure metering pump to deliver 2815kg (the molar ratio of ammonia to cyclopropane is 6), cyclopropane and ammonia water After fully mixing, enter the preheater, preheat to 140°C, and then enter the reactor with temperature controlled at 151-154°C and pressure controlled at 16.8-17.0Mpa. After fully reacting for 3 hours, the reaction mixture product first enters flash evaporation Tower, the pressure is controlled at 1.5Mpa, the temperature of the tower bottom is controlled at 155-158°C, excess ammonia is recovered, the materials in the flash tower bottom are sent to the dehydration tower for rectification and dehydration, the pressure of the dehydration tower is controlled at -0.085Mpa, and the temperature of the top of the tower is controlled At 46-47°C, the temperature of the tower bottom is controlled a...

Embodiment 2

[0017] Fully mix 4925kg liquid ammonia and 75kg deionized water to form ammonia water (water 1.5%), transport it with a high-pressure metering pump, and then use another high-pressure metering pump to deliver 2400kg (the molar ratio of ammonia to cyclopropane is 7), cyclopropane and ammonia water After fully mixing, enter the preheater, preheat to 142°C, and then enter the reactor with temperature controlled at 152-155°C and pressure controlled at 17.0-17.3Mpa. After fully reacting for 2.5 hours, the reaction mixture product first enters flash evaporation Tower, the pressure is controlled at 1.0Mpa, the temperature of the tower bottom is controlled at 155-158°C, excess ammonia is recovered, the materials in the flash tower bottom are sent to the dehydration tower for rectification and dehydration, the pressure is controlled at -0.082Mpa, and the temperature at the top of the tower is controlled at 53 ~54°C, the temperature of the tower bottom is controlled at 123-125°C, the pre...

Embodiment 3

[0019] Fully mix 4875kg liquid ammonia and 125kg deionized water to form ammonia water (water 2.5%), transport with high-pressure metering pump, and then use another high-pressure metering pump to transport 2079kg (the molar ratio of ammonia to cyclopropane is 8), cyclopropane and ammonia water After fully mixing, enter the preheater, preheat to 143°C, and then enter the reactor with the temperature controlled at 149-152°C and the pressure controlled at 17.2-17.5Mpa. After fully reacting for 2.0 hours, the reaction mixture product first enters flash evaporation Tower, the pressure is controlled at 0.8Mpa, the temperature of the tower bottom is controlled at 145-148°C, excess ammonia is recovered, the materials in the flash tower bottom are sent to the dehydration tower for rectification and dehydration, the pressure is controlled at -0.085Mpa, and the temperature at the top of the tower is controlled at 46 ~47°C, the temperature of the tower bottom is controlled at 114-115°C, t...

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

No PUM Login to View More

Abstract

The invention relates to a method of manufacturing diisopropanolamine. Liquid ammonia and water are mixed to form ammonia water which is fully mixed with propylene oxide; the mixed solution is preheated until the temperature reach 140 to 145 DEG C and then is delivered into a reactor for reacting, the temperature is controlled within 148 to 155 DEG C when in reacting, the pressure is controlled within 16.0 to 18.0MPa, the inputting molar ratio of the ammonia and the propylene oxide is controlled within 5 to 8, and the reaction is fully performed for 1.5 to 3 hours; the mixture products obtained in the reaction are separated to obtain isopropanolamine products, diisopropanolamine products and triisopropanolamine products through flash evaporation and rectification in a stepwise way. In the diisopropanolamine products which are manufactured by adopting the method, the component of 1, 1<1>-nitrousalkyl-dipropyl-2-alcohol accounts for more than 99 percent (hereinafter referred to as mass percent), and the isomeride thereof is less than 1 percent. In addition, the cost of the production operation in the method is less, the production cost is low, the product quality is high, and the high-end requirement of products such as synthetic medicine, farm insecticide, etc. is satisfied.

Description

technical field [0001] The invention relates to a method for preparing diisopropanolamine. Background technique [0002] Diisopropanolamine is 1,1'-azinoalkyldipropan-2-alcohol (chemical formula: [CH 3 CH(OH)CH 2 〕 2 The common name of NH) is a derivative formed by the reaction of one isopropanolamine and propylene oxide. Diisopropanolamine has a wide range of uses as follows: it can be used as a foam stabilizer for detergents and a pesticide neutralizer; it can be used as a wax, fiber auxiliary, insecticide, emulsifier, and dispersant; it can be used as a high-efficiency desulfurizer ; Used as synthesis gas CO in synthetic ammonia industry 2 remover etc. [0003] Most of the industrial production of diisopropanolamine now uses ammonia water or liquid ammonia and propylene oxide as raw materials to synthesize isopropanolamine series mixtures, and then separates monoisopropanolamine, diisopropanolamine, and triisopropanolamine step by step. The method of propanolamine, ...

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): C07C215/12C07C213/04
Inventor 张书芮益民韦华
Owner NANJING BAOCHUN CHEMICAL INDUSTRY CO LTD
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com