Bisphenol A salt preparation method

A bisphenol and inorganic technology, applied in the field of bisphenol A salt preparation, can solve the problems of complex equipment, poor product purity, and low reaction efficiency, and achieve the effects of simple equipment, less waste, and high solid content

Active Publication Date: 2020-03-13
WANHUA CHEM GRP CO LTD
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This technology improves the yield rate for producing phenolsulfonate esters (PES). It eliminates the use of harmful chemical substances like dimethyl sulfite or dichloromaleimide which could cause environmental concerns. Additionally, it increases the quality of PES produced with this method without adding any extra steps. Overall, these technical improvements improve the performance and cost-effectiveness of making polyetherester resin materials.

Problems solved by technology

Technological Problem: Current methods for producing highly pure diarylethane bonds involve complicated processes involving multiple reactions, which can result in decreased yields due to decomposition products from unstable acid chelating agents during storage. There remains a technical challenge towards developing simpler and more effective ways to produce these materials without decompositing them over time.

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
  • Bisphenol A salt preparation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] Accurately weigh 22.83g of bisphenol A and 5g of sodium hydroxide solid, put them into an ultrafine pulverizer and pulverize to obtain a mixture powder with a particle size of 2500 mesh. Put the resulting mixture into a round-bottomed flask connected with an air inlet conduit, a gas moisture tester, an anchored stirring paddle, and a vacuum pump, and simultaneously feed argon gas at a rate of 1.5 L / min. ℃. The round-bottomed flask was heated to 180° C. through a salt bath, and the stirring was started to 60 rpm. When no moisture content is detected at the gas outlet, close the inlet valve and increase the temperature to 250°C. At the same time, turn on the vacuum pump until the vacuum degree is -0.05MPa, and stop heating after 1 hour of vacuum distillation. Finally, 16.47 g of bisphenol A sodium salt solid was obtained, with a yield of 96.75% (based on sodium hydroxide). Elemental analysis test shows that the content of sodium element is 16.74% (theoretical value is 16

Embodiment 2

[0033] 228.3g of bisphenol A and 31.92g of lithium hydroxide were put into an ultrafine pulverizer, and were thoroughly pulverized to obtain an ultrafine mixture powder with a particle size of 3500 mesh. Add the mixed powder into the reactor, which is connected with an air inlet duct, a gas moisture tester, an anchor stirring paddle and a vacuum pump, and the reactor is fed with nitrogen in advance to exhaust the air. The temperature of the reaction kettle was gradually raised to 160° C., and the stirring speed was set at 50 rpm. After starting the reaction, pass the nitrogen gas heated to 160°C by the air heater into the reaction kettle at a flow rate of 0.5L / min, and monitor the moisture in the discharged nitrogen gas with a gas moisture tester, and stop when no moisture is produced. reaction. Close the inlet valve, raise the temperature of the kettle to 220° C., and turn on the vacuum pump to a vacuum degree of -0.1 MPa, and distill the excess bisphenol A under reduced pres

Embodiment 3

[0035] Grind 42.53g of potassium carbonate flaky solid into coarse particles, then mix with 91.32g of bisphenol A particles, put them into an ultrafine pulverizer for further pulverization and mixing, and finally obtain an ultrafine powder with a particle size of 3000 mesh. Then pour the pulverized mixture into the stainless steel reactor that has been installed with an air inlet duct, a gas moisture tester, an anchor paddle and a vacuum pump in advance, and the reactor is protected by carbon dioxide through the air inlet pipe. The reactor was heated to 170° C., the stirring speed was 100 rpm, and carbon dioxide gas previously heated to 170° C. by an air heater was passed into the reactor at a flow rate of 2 L / min. As the reaction progresses, the moisture content is monitored through a gas moisture tester connected to the gas outlet until no more moisture is produced to stop the reaction and close the inlet valve. Continue to raise the temperature of the reactor to 230°C, turn

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 provides a bisphenol A salt preparation method, wherein bisphenol A and an inorganic strong base are directly subjected to a solvent-free reaction to obtain a bisphenol A salt. The preparation method comprises the following steps: (1) crushing and mixing bisphenol A and an inorganic strong base to obtain an ultrafine mixture; (2) heating and stirring the mixture, and carrying out a reaction to obtain a crude product; and (3) carrying out reduced pressure distillation on the crude product to remove residual excessive bisphenol A, and cooling to obtain bisphenol A salt solid powder. The method has the advantages that no solvent is used in the whole reaction process, the reaction is simple and rapid, the yield is high, and the product purity is high.

Description

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

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
Owner WANHUA CHEM GRP CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products