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

Method for synthesizing polyethylene glycol monomethacrylate from solid superacid by catalytic esterification

A technology of monomethacrylate and solid superacid, which is applied in the preparation of carboxylic acid esters, the preparation of organic compounds, organic chemistry, etc., and can solve the problems of difficult recycling, waste, and excessive methacrylic acid

Inactive Publication Date: 2012-05-30
WUHAN UNIV OF SCI & TECH
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] At present, esters of synthetic polyethylene glycol systems are widely used in the surfactant industry. Chen Jianqin and Lin Zhiyong used solid super acid SO 4 2- / ZrO 2 Catalytic esterification of industrial oleic acid and polyethylene glycol to synthesize polyethylene glycol oleate for leather products; Qilu Petrochemical Company's patent CN 1208032A uses activated carbon, silica to absorb sulfuric acid, p-toluenesulfonic acid, etc. as solid acids to prepare formazan Higher esters of acrylic acid; Li Jinbiao and other published patents CN 101544729A utilize allyl polyethylene glycol and acrylic acid to prepare allyl polyethylene glycol acrylate, and are used to prepare monomers for water reducers; patent CN1636921 introduces that the degree of polymerization is 5 ~40 polyethylene glycol and acrylic acid are the main raw materials, p-toluenesulfonic acid is used as catalyst, hydroquinone is used as polymerization inhibitor, cyclohexane is used as water-carrying agent, and the reaction is carried out at 80~90℃ for 8±0.5 hours to form Polyethylene glycol monoacrylate is used as a macromonomer for the synthesis of polycarboxylate water reducers; Sun Risheng of Nanchang University used polyethylene glycol and methacrylic acid in a molar ratio of 1: 2. Polyethylene glycol monomethacrylate is synthesized, but it is not indicated in the text whether it is a diester or a monoester. At the same time, there is a large excess of methacrylic acid, which is easy to cause waste and difficult to recycle.
And using solid superacid SO 4 2- / ZrO 2 Esterification of polyethylene glycol monomethacrylate as a macromonomer for the synthesis of polycarboxylate superplasticizers has not been reported at home and abroad

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

[0030] Install a stirring device, a condenser, a water separator and a thermometer on a 250ml three-necked flask. Add the methacrylic acid of 1.1mol, the polyethylene glycol (molecular weight 400) of 1.0mol, the solid superacid SO of 3.0% (relative to the quality of total feeding) 4 2- / ZrO 2 Catalyst, 20% (relative to the quality of the total feed) of water-carrying agent cyclohexane, 0.5% (relative to the quality of methacrylic acid) of hydroquinone, carry out air bath heating with an electric kettle, and start stirring. From the water-carrying agent and the water generated by the reactant to azeotrope, react at a temperature of 85°C for 20 hours. Under normal pressure, the water is removed by azeotropy through the water separator, and the water agent is returned to the three-necked bottle for recycling. The esterified product is filtered to separate the solid superacid SO 4 2- / ZrO 2 catalyst, and the filtrate was distilled under reduced pressure to recover cyclohexan...

Embodiment 2

[0033] Stirring device, condenser, water separator and thermometer are installed on the 250ml three-necked flask; Strong acid (SO 4 2- / ZrO 2 ) catalyzer, 80% (relative to the quality of total feed intake) water-carrying agent xylene, 0.25% (relative to the quality of methacrylic acid feed intake) hydroquinone, carry out air bath heating with electric kettle, start stirring. From the azeotropic start of the water-carrying agent and the water generated by the reactants, the reaction was carried out at a temperature of 135° C. for 12 hours. Under normal pressure, the water is removed by azeotropy through the water separator, and the water agent is returned to the three-necked bottle for recycling. The esterified product is filtered to separate the solid superacid SO 4 2- / ZrO 2Catalyst, the filtrate recovers xylene through vacuum distillation to obtain polyethylene glycol monomethacrylate (PEGMA) macromonomer. Recovered solid superacid SO 4 2- / ZrO 2 And xylene can be ...

Embodiment 3

[0036] Install a stirring device, a condenser, a water separator and a thermometer on a 250ml three-necked flask. Add the methacrylic acid of 1.5mol, the polyethylene glycol (molecular weight 4000) of 1.0mol, the solid superacid SO of 5.0% (the quality of relative total feeding) 4 2- / ZrO 2 Catalyst, 80% (relative to the quality of total feeding) of water-carrying agent toluene, 0.2% (relative to the quality of methacrylic acid feeding) of hydroquinone, carry out air bath heating with electric kettle, start stirring. From the azeotropic start of the water-carrying agent and the water generated by the reactants, the reaction was carried out at a temperature of 145° C. for 6 hours. Under normal pressure, the water is azeotropically removed through the water separator, and the water agent is returned to the three-necked bottle for recycling. The esterified product is filtered to separate the solid superacid SO 4 2- / ZrO 2 Catalyst, filtrate recovers toluene through decompre...

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 discloses a method for synthesizing polyethylene glycol monomethacrylate from solid superacid by catalytic esterification. The method takes polyethylene glycol and methacrylic acid as reactants, uses a solid superacid SO4<2-> / ZrO2 as a catalyst, and comprises the steps of adding a polymerization inhibitor, heating and carrying out a reflux reaction, adding a water-carrying agent toluene to continuously remove water generated in the reaction, filtering, recovering the solid superacid SO4<2-> / ZrO2 after the reaction, and purifying the product under the condition of reduced pressure distillation to directly obtain the polyethylene glycol monomethacrylate, i.e. a macromonomer polyethylene glycol monomethacrylate for synthesizing a polycarboxylic acid water reducer. The conversion rate based on the polyethylene glycol is above 98.1%, and the yield of ester is above 98%. The recovered water-carrying agent and the recovered solid superacid SO4<2-> / ZrO2 can be recycled.

Description

technical field [0001] The invention relates to the field of fine chemicals, in particular to a method for synthesizing polyethylene glycol monomethacrylate (PEGMA). The synthesized macromonomer is used in the synthesis of polycarboxylate water reducer. Background technique [0002] At present, esters of synthetic polyethylene glycol systems are widely used in the surfactant industry. Chen Jianqin and Lin Zhiyong used solid super acid SO 4 2- / ZrO 2 Catalytic esterification of industrial oleic acid and polyethylene glycol to synthesize polyethylene glycol oleate for leather products; Qilu Petrochemical Company's patent CN 1208032A uses activated carbon, silica to absorb sulfuric acid, p-toluenesulfonic acid, etc. as solid acids to prepare formazan Higher esters of acrylic acid; Li Jinbiao and other published patents CN 101544729A utilize allyl polyethylene glycol and acrylic acid to prepare allyl polyethylene glycol acrylate, and are used to prepare monomers for water red...

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): C08G65/48C07C69/54C07C67/08C08F290/06C04B24/26C04B103/30
CPCY02P20/584
Inventor 廖国胜冯为民唐红钟侚
Owner WUHAN UNIV OF SCI & TECH
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