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

Continuous production method for perfluoro tripropylamine

A technology of perfluorotripropylamine and its production method, which is applied in chemical instruments and methods, preparation of organic compounds, preparation of amino compounds, etc., can solve the problems of many by-products, non-continuous production, low yield, etc., so as to improve production Efficiency, the effect of reducing breakage

Active Publication Date: 2014-07-16
苏州工业园区捷仕通医疗设备有限公司
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The cobalt trifluoride fluorination method needs to convert cobalt oxide or cobalt dioxide into cobalt trifluoride by fluorination first, and then cobalt trifluoride reacts with tripropylamine in the reactor to obtain a mixture containing perfluorotripropylamine; cobalt fluoride Continuous regeneration is required, the temperature of the reactor is difficult to control uniformly, the amplification is limited, the production cannot be carried out continuously, and it is not suitable for mass production
In addition, the electrolytic synthesis of perfluorotripropylamine has complicated equipment, difficult condition control, many by-products, and low yield, generally no more than 30%.

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

[0025] In the monel alloy fluorination reactor with an inner diameter of 80 mm and a length of 200 mm, spherical cobalt oxide with a diameter of 3 mm is filled. The fluorination reactor is heated to 300°C, and a mixed gas of 50% fluorine and 50% nitrogen is introduced for fluorination, so that cobalt oxide is completely converted into cobalt trifluoride. Then maintain the temperature of the fluorination reactor at 230°C; continuously feed 20% fluorine-nitrogen mixed gas and 10% tripropylamine-nitrogen mixed gas in the ratio of 10:1 molar ratio of fluorine gas to tripropylamine for reaction, and control the residence time for 5 Second. After 3 hours, neutralize the collected reaction product with 20% potassium hydroxide aqueous solution until the pH value is neutral, let it stand, after layering, take the organic phase and wash it with deionized water three times, separate the organic phase and wash it with anhydrous sodium sulfate After drying, carry out rectification and sep...

Embodiment 2

[0027] Using the same equipment as in Example 1, the fluorination reactor was heated to 300°C, and a 50% fluorine-50% nitrogen mixed gas was introduced for fluorination, so that cobalt oxide was completely converted into cobalt trifluoride. Then maintain the temperature of the fluorination reactor at 200°C; continuously feed 20% fluorine-nitrogen mixed gas and 15% tripropylamine-nitrogen mixed gas in the ratio of 12:1 molar ratio of fluorine gas to tripropylamine to react, and control the residence time for 5 Second. After 3 hours, neutralize the collected reaction product with 20% potassium hydroxide aqueous solution until the pH value is neutral, let it stand, after layering, take the organic phase and wash it with deionized water three times, separate the organic phase and wash it with anhydrous sodium sulfate After drying, carry out rectification and separation, take the boiling point of 127 ~ 128 ℃ for fractionation, and obtain perfluorotripropylamine with a purity of 98%...

Embodiment 3

[0029] Using the same equipment as in Example 1, the fluorination reactor was heated to 260°C, and a 50% fluorine-50% nitrogen mixed gas was introduced for fluorination, so that cobalt oxide was completely converted into cobalt trifluoride. Then the temperature of the fluorination reactor is maintained at 260°C; 30% fluorine-nitrogen mixed gas and 20% tripropylamine-nitrogen mixed gas are continuously fed into the reaction according to the molar ratio of fluorine gas to tripropylamine 16:1, and the residence time is controlled for 5 Second. After 3 hours, neutralize the collected reaction product with 20% potassium hydroxide aqueous solution until the pH value is neutral, let it stand, after layering, take the organic phase and wash it with deionized water three times, separate the organic phase and wash it with anhydrous sodium sulfate After drying, carry out rectification and separation, take the boiling point of 127 ~ 128 ℃ for fractionation, and obtain perfluorotripropylam...

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
diameteraaaaaaaaaa
Login to View More

Abstract

The invention discloses a continuous production method for prefluoro tripropylamine. The continuous production method for prefluoro tripropylamine comprises the following steps of: (1) filling filler into a fluoration reactor, and then introducing fluorine mixed gas for fluoridizing; (2) adding tripropylamine into a tripropylamine vaporizer by a feeder; (3) introducing nitrogen into the tripropylamine vaporizer, diluting tripropylamine steam and continuously carrying the diluted tripropylamine into the fluoration reactor; (4) continuously introducing fluorine nitrogen mixed gas into the fluoration reactor to react with the diluted tripropylamine steam mixed gas continuously introduced into the fluoration reactor, and collecting reaction products; and (5) washing the reaction products with alkali, then washing with water, rectifying and purifying to finally obtain prefluoro tripropylamine. According to the continuous production method for prefluoro tripropylamine, fluorine simple substance or diluent fluorine gas is adopted as an activating agent, and feeding ratio of a fluoration agent to tripropylamine, reaction temperature and reaction time are accurately controlled, so that organic reactant is fluorated completely; and breakage of intramolecular C-C bonds is reduced to the utmost extent, and production efficiency of the prefluoro tripropylamine target product is improved.

Description

technical field [0001] The invention relates to a continuous production method of artificial blood raw materials and perfluorotripropylamine, a special working medium used in the manufacturing process of semiconductor devices. Background technique [0002] In the past, the preparation methods of perfluorotripropylamine include cobalt trifluoride fluorination method and electrolytic fluorination method. The cobalt trifluoride fluorination method needs to convert cobalt oxide or cobalt dioxide into cobalt trifluoride by fluorination first, and then cobalt trifluoride reacts with tripropylamine in the reactor to obtain a mixture containing perfluorotripropylamine; cobalt fluoride Continuous regeneration is required, the temperature of the reactor is difficult to control uniformly, the amplification is limited, the production cannot be carried out continuously, and it is not suitable for mass production. In addition, the electrolytic synthesis of perfluorotripropylamine is comp...

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 Patents(China)
IPC IPC(8): C07C211/15C07C209/74
Inventor 鲁俞方治文
Owner 苏州工业园区捷仕通医疗设备有限公司
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