Unlock instant, AI-driven research and patent intelligence for your innovation.

Method for preparing polyacrylic acid composite macromolecular hydrogel by macromolecular chain template method

A technology of compounding macromolecules and macromolecular chains, applied in the field of polyacrylic acid compound hydrogel and its preparation, can solve the problem of weak mechanical strength and healing ability of gel, inability to self-repair to the original state, difficult to apply soft tissue materials, etc. problems, to achieve the effect of improving self-healing performance and mechanical properties, simple self-healing process, and excellent mechanical properties

Active Publication Date: 2017-06-13
SOUTHEAST UNIV
View PDF4 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] There have also been a lot of reports on self-healing polymer gels in recent years, but due to their extremely small internal energy dissipation, the mechanical strength of the gels has been greatly reduced.
Moreover, due to the lack of combined reorganization mechanism, once the gel structure is damaged and broken, it cannot repair itself to the original state
Due to the weak mechanical strength and healing ability of the gel, it is difficult to apply to actual soft tissue materials, such as artificial cartilage, etc.

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
  • Method for preparing polyacrylic acid composite macromolecular hydrogel by macromolecular chain template method
  • Method for preparing polyacrylic acid composite macromolecular hydrogel by macromolecular chain template method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] 1) Add 5 g of amino-terminated polyethylene glycol (PEG 500 ) was dissolved in 10 mL of anhydrous dichloromethane, added 0.05 mL of triethylamine, N 2 protection, stirred in ice bath for 1 h; then added 0.05 g of 2,6-pyridinedicarbonyl chloride, continued to stir for 1 h in ice bath, and finally added 10 mL of methanol to quench the reaction, precipitated and washed 3 times in diethyl ether, at 50 °C Vacuum dry.

[0029] 2) Add 0.25 g of extended chain PEG 500 Dissolve in 5 mL of deionized water, then add 2 g of acrylic acid monomer and stir for 20 min.

[0030] 3) Add 0.025 g FeCl 3 In the above mixture, continue to stir for 20 min.

[0031] 4) Add 0.025 g of ammonium persulfate to the above solution and continue stirring for 5 min.

[0032] 5) Inject the above liquid into a specific mold and react at 25°C for 2 h.

[0033] 6) The prepared composite hydrogel was taken out and immersed in deionized water for 24 h to remove unreacted monomers, initiators and metal ...

Embodiment 2

[0036] 1) Add 5 g of amino-terminated polyethylene glycol (PEG 1000 ) was dissolved in 20 mL of anhydrous dichloromethane, added 0.5 mL of triethylamine, N 2 protection, stirred in ice bath for 1 h; then added 0.5 g of 2,6-pyridinedicarbonyl chloride, continued to stir for 1 h in ice bath, and finally added 10 mL of methanol to quench the reaction, precipitated and washed 3 times in ether, at 50 °C Vacuum dry.

[0037] 2) Add 0.25g chain extension PEG 1000 Dissolve in 5 mL of deionized water, then add 2 g of acrylic acid monomer and stir for 20 min.

[0038] 3) Add 0.05 g FeCl 3 In the above mixture, continue to stir for 20 min.

[0039] 4) Add 0.05 g of ammonium persulfate to the above solution and continue stirring for 5 min.

[0040] 5) Inject the above liquid into a specific mold and react at 25°C for 6 h.

[0041] 6) The prepared composite hydrogel was taken out and immersed in deionized water for 24 h to remove unreacted monomers, initiators and metal ions.

[004...

Embodiment 3

[0044] 1) Add 5 g of amino-terminated polyethylene glycol PEG 2000Dissolve in 20 mL of anhydrous dichloromethane, add 0.25 mL of triethylamine, N 2 Protected, stirred in ice bath for 2 h; then added 0.25 g of 2,6 pyridinedicarbonyl chloride, continued to stir for 2 h in ice bath, finally added 5 mL of methanol to quench the reaction, washed the precipitate in diethyl ether for 5 times, and dried in vacuum at 50 °C .

[0045] 2) Add 0.5 g chain-extended PEG 2000 Dissolve in 10 mL of deionized water, then add 2 g of acrylic acid monomer and stir for 20 min.

[0046] 3) Add 0.1 g FeCl 3 In the above mixture, continue to stir for 20 min.

[0047] 4) Add 0.1 g of ammonium persulfate to the above solution, and continue stirring for 5 min.

[0048] 5) Inject the above liquid into a specific mold and react at 25°C for 6 h.

[0049] 6) The prepared composite hydrogel was taken out and immersed in deionized water for 24 h to remove unreacted monomers, initiators and metal ions.

...

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 preparing polyacrylic acid composite macromolecular hydrogel by a macromolecular chain template method. The macromolecular hydrogel with high mechanical strength and self-repairing property is prepared by taking a macromolecular chain with a coordination function as a template and by guiding an acrylic acid monomer to coordinate and polymerize under the coordination action of metal ions. The self-repairing hydrogel comprises the following raw material components in part by mass: 2.5 to 10 parts of a macromolecular template, 5 to 25 parts of monomers, 30 to 60 parts of water, 0.1 to 2.5 parts of metal ions and 0.1 to 2.5 parts of an initiator. The method is characterized in that preparation of a regular polymer is effectively guided under the existence of the macromolecular template; and the mechanical strength and the self-repairing capability of the hydrogel are enhanced. The composite hydrogel prepared by the method has excellent mechanical performance and excellent self-repairing performance at normal temperature.

Description

technical field [0001] The invention belongs to the field of self-repairing polymer hydrogels, and relates to a polyacrylic acid composite hydrogel with high self-repairing performance and excellent mechanical properties and a preparation method thereof. Background technique [0002] The design of polymer network structure has become a hotspot in the field of polymer research. The preparation method is mainly through the action of covalent bond and non-covalent bond (hydrogen bond, ionic bond, etc.). Due to the strong covalent bond, the polymer network structure loses the ability to recombine after being damaged, which limits the wide application of polymer materials. However, weaker hydrogen bonds or ionic bonds have the ability to recombine after breaking, which greatly improves the application range of polymer network structures. The specific structure and properties of some organisms in nature provide inspiration and inspiration for human beings in the process of con...

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
IPC IPC(8): C08F120/06C08L33/02C08L71/02C08K3/16C08J3/075
CPCC08F120/06C08J3/075C08J2333/02C08J2471/02C08L33/02C08L71/02C08K3/16
Inventor 付国东马强刘顺利姚芳
Owner SOUTHEAST UNIV