Method for synthesizing hydrogel

A technology of hydrogel and methacrylic acid, applied in the field of synthetic hydrogel, can solve the problems of slow stimulus response, limited application, lack of regularity, etc., and achieves the advantages of being beneficial to industrial production, good biocompatibility, and simple preparation method. Effect

Inactive Publication Date: 2009-10-14
SUZHOU UNIV
View PDF0 Cites 20 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The main disadvantages of these methods are: due to the high polymerization rate of conventional free radical polymerization and the thermal effect, chain transfer, chain termination reaction and self-acceleration phenomenon in the reaction process, the synthesized gel cannot control the cross-linking density and cross-linking density of the network. The molecular mass of the chain segments between the linking points and the distribution of cross-linking points are uneven and difficult to control. The structure of the synthesized polymer gel is in an amorphous state, without regularity, slow response to external environmental stimuli, and no synergy. Therefore, the synthesis The properties of the obtained gel are not ideal, which limits its application in material synthesis
[0007] However, the above method is used to synthesize linear polymers and does not involve the field of hydrogel synthesis; in addition, the catalysts involved in the above methods are basically limited to copper salt catalytic systems, and copper salt catalytic systems are due to their inherent biological toxicity. When it is applied to the synthesis of smart hydrogel materials with good biocompatibility, there is a problem of bringing greater toxicity to the materials.

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 synthesizing hydrogel
  • Method for synthesizing hydrogel
  • Method for synthesizing hydrogel

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Synthesis of PPEGMA Hydrogel Using Br-PEG-Br as Initiator

[0034] According to the ratio n(PEGMA):n(Br-PEG-Br):n(EGDMA):n(FeCl 3 .6H 2 O):n(TDA-1):n(VC)=500:1:5~40:3:9:5, add FeCl 3 .6H 2 O, TDA-1, PEGMA (2mL), EGDMA, Br-PEG-Br and VC in 10mL ampoules, sealed directly under air atmosphere (bulk polymerization). If solution polymerization is used, add 2 mL of deionized water after adding all the above chemical reagents and seal the tube directly under air atmosphere. The sealed ampoule was placed in an oil bath at a constant temperature (90° C.) for a predetermined time to react (3˜46 h). After the reaction is over, take out the sealed tube, immediately cool it with cold water, open the sealed tube, soak and filter with an appropriate amount of deionized water, and freeze-dry to obtain a xerogel.

[0035] Using macromolecular bifunctional initiator (Br-PEG-Br), by changing the amount of crosslinking agent (EGDMA), the liquid absorption rate of the obtained polymer ...

Embodiment 2

[0041] Synthesis of PPEGMA Hydrogel Prepared with DMDBH as Initiator

[0042] According to the ratio n(PEGMA):n(DMDBH):n(EGDMA):n(FeCl 3 .6H 2 O):n(TDA-1):n(VC)=500:1:10~30:3:9:3, add FeCl in sequence 3 .6H 2 O, TDA-1, PEGMA (2mL), EGDMA, DMDBH, VC and deionized water (2mL) were directly capped in a 10mL ampoule under air atmosphere. The sealed ampoule was placed in an oil bath at a constant temperature (90° C.) for a predetermined time to react (18-21 h). After the reaction is over, take out the sealed tube, immediately cool it with cold water, open the sealed tube, soak and filter with an appropriate amount of deionized water, and freeze-dry to obtain a xerogel.

[0043] Using a small molecule initiator (DMDBH), by changing the amount of crosslinking agent (EGDMA), the data of the liquid absorption rate of the obtained polymer hydrogel (with deionized water and methanol as the solvent to be absorbed) are shown in Table 2 Show. It can be seen from the data in the table ...

Embodiment 3

[0048] Synthesis of PDMAEMA Hydrogel

[0049] According to the ratio n(DMAEMA):n(DMDBH or Br-PEG-Br):n(EGDMA):n(FeCl 3 .6H 2 O):n(TDA-1):n(VC)=500:1:1~5:3:9:1~5, add FeCl in sequence 3 .6H 2 O, TDA-1, PEGMA (2mL), EGDMA, DMDBH or Br-PEG-Br and VC in 10mL ampoules were directly sealed under air atmosphere. The sealed ampoule was placed in an oil bath at a constant temperature (90° C.) for a predetermined time to react (1˜4 h). After the reaction is finished, take out the sealed tube, immediately cool it with cold water, open the sealed tube, soak and filter with an appropriate amount of deionized water, freeze-dry to obtain a xerogel.

[0050] Adopting small molecule bifunctional initiator (DMDBH), by changing the consumption of cross-linking agent (EGDMA), the data of the liquid absorption rate of the obtained polymer hydrogel (respectively with deionized water and methanol as the solvent to be absorbed) are shown in the table 3 (number 1, 2, 3). It can be seen from the ...

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 hydrogel, one out of N, N-(dimethylamino) ethyl methacrylate or methylacrylic acid polyethylene glycol single methyl ether ester is taken as a monomer, the monomer, an initiator, a cross-linking agent, a catalyst, a complexing agent and a reductant are added according to the molar ratio that monomer: initiator: cross-linking agent: catalyst: complexing agent and reductant is equal to 100-1000: 1: 1-50: 0.05-3: 0.15-9: 1-10, so as to carry out the AGET ATRP reaction and synthesize the hydrogel; wherein the initiator is selected from one out of polyethylene glycol bis (alpha-bromoisobutyrate) ester or 2,6-dibromo dimethyl heptanedioate; the cross-linking agent is one out of ethylene glycol dimethacrylate or poly(ethylene glycol) dimethacrylate; and the catalyst is selected from one out of hexahydrated high ferric chloride or ferric bromide. The method can control the crosslinking degree by regulating the using amount of the cross-linking agent, so that the method can control the mesh size of the hydrogel, control the liquid absorption performance of the hydrogel and obtain the hydrogel with good biocompatibility.

Description

technical field [0001] The invention relates to a method for preparing a gel, in particular to a method for synthesizing a hydrogel. Background technique [0002] The colloidal particles or polymers in the sol or solution are connected to each other under certain conditions to form a space network structure, which is filled with liquid as a dispersion medium. Such a special dispersion system is called gel. Due to the affinity between the liquid and the polymer network, the liquid is enclosed by the polymer network and loses its fluidity, so the gel can display a certain shape like a solid. During the swelling process of the gel, on the one hand, the solvent tries to penetrate into the polymer to expand its volume, and on the other hand, due to the volume expansion of the cross-linked polymer, the molecular network is subjected to stress and shrinks. When these two opposite tendencies compete with each other , reaching the swelling equilibrium. The swelling behavior of poly...

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): C08F220/34C08F220/28C08F2/02C08F2/04C08F4/26
Inventor 程振平何伟伟朱秀林朱高华张丽芬朱健张正彪
Owner SUZHOU UNIV
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