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

Synthesis of fused liquid crystal of chitosan grafted polylactic acid

A synthesis method, chitosan technology, applied in the field of synthesis of chitosan-grafted polylactic acid melt-induced liquid crystals, can solve the problems of application limitations, unclear physiological effects of polyvinyl alcohol, poor hydrophilicity, etc., and achieve excellent biophase Capacitance, excellent biodegradability, effect of improving solubility

Inactive Publication Date: 2003-01-01
SHANGHAI JIAO TONG UNIV
View PDF0 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the poor hydrophilicity of its surface, the degradation time in the human body is long, so that it causes adverse reactions in the body
For a long time, people have used other hydrophilic and water-soluble materials to improve the surface hydrophilic properties of polylactic acid, such as Breitenbach and his collaborators, (Polymer, Vol.39, No.14, p3261-3271, 1998.) Water-soluble polyvinyl alcohol is used as the backbone to synthesize a graft copolymer of polyvinyl alcohol and polylactic acid, but the physiological role of polyvinyl alcohol is still unclear, so its application is limited

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

[0012] Implementation of chitosan with 50% deacetylation degree and lactide molar ratio of 1:1.

[0013] The chitosan with a deacetylation degree of 50% was dried in a vacuum oven for 48 hours to remove the adsorbed water on its surface. Weigh 0.05 mol of chitosan and add it to the reactor, pour nitrogen into it repeatedly three times, then degas under vacuum for 1 hour, add 40 ml of dried toluene as a dispersant, and prepare it into a 1.25 mol toluene dispersion . Weigh 0.05 mol of triethylaluminum to prepare a 15% toluene solution. Add the triethylaluminum solution dropwise to the chitosan toluene dispersion at room temperature, and react for another 1 hour when no gas is generated. Add 0.05 mol of lactide degassed by vacuum for 1 hour, then place the reactor in an oil bath pre-heated to 70°C, react for more than 20 hours, pour the reaction solution into ethanol to allow it to fully precipitate, and filter and dry After obtaining the product. Because the deacetylation de...

Embodiment 2

[0015] The implementation of chitosan and lactide with a degree of deacetylation of 94% at a ratio of 1:1.

[0016] The chitosan with a deacetylation degree of 94% was dried in a vacuum oven for 48 hours to remove the adsorbed water on its surface. Weigh 0.05mol chitosan and add it into the reactor, flush with nitrogen three times, and then degas under vacuum for 1 hour. Add 60 ml of dried toluene as a dispersant to prepare a 0.83 mole toluene dispersion. Weigh 0.05 mol of triethylaluminum to prepare a 15% toluene solution. Add the triethylaluminum solution dropwise to the chitosan toluene dispersion at room temperature, and react for another 1 hour when no gas is produced. Add 0.05 mol of lactide that has been vacuum degassed for 1 hour, then place the reactor in an oil bath pre-heated to 70°C, and after 20 hours of reaction, pour the reaction solution into ethanol to make it fully precipitate, filter and dry After obtaining the product. In this embodiment, chitosan with ...

Embodiment 3

[0018] Acetyl degree 94% chitosan and lactide 1:60 implementation.

[0019] The chitosan with a deacetylation degree of 94% was dried in a vacuum oven for 48 hours to remove the adsorbed water on its surface. Weigh 0.005 mol of chitosan and add it into the reactor, flush with nitrogen for three times, and then degas under vacuum for 1 hour. Add 100 ml of dried toluene as a dispersant to prepare a 0.05 mol toluene dispersion. Weigh 0.005 mol of triethylaluminum to prepare a 15% toluene solution. Add the triethylaluminum solution dropwise to the chitosan toluene dispersion at room temperature, and react for another 1 hour when no gas is produced. Add 0.3 mol of lactide that has been vacuum degassed for 1 hour, then place the reactor in an oil bath preheated to 70°C, and after 20 hours of reaction, pour the reaction solution into ethanol to make it fully precipitate, filter and dry After obtaining the product. Due to the use of chitosan with a high degree of deacetylation and...

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 synthesis of fused liquid crystal of chitosan grafted polylactic acid includes vacuum deairing of chitosan for 1 hr, charging nitrogen, adding toluene as dispersant, dripping toluene solution of aluminium ethide as catalyst in 1-3 molar times of chitosan, ring opening polymerization of lactide inside solution to produce grafted copolymer of chitosan and polylactic acid. The grafted copolymer of the present invention has special performance, and may be used as interface coupling agent for polymer blend of chitin, chitosan and polylactic acid as well as medicine delayed releasing material and other human body implanting biological material. In addition, it has the performance of fused liquid crystal and thus may be produced into various biological material.

Description

Technical field: [0001] The invention relates to a method for synthesizing chitosan-grafted polylactic acid melt-tropic liquid crystals. During the heating process, the synthesized material can appear in the melting state of chitosan, which does not exist in the heating process, so the chitosan can be enlarged. Processing range, such as high-strength fibers obtained by melt spinning in a liquid crystal state, may be used as sutures for surgical operations and reinforcing fibers for other biocomposites; and directly processed into other biomaterial-related products in a molten state. Background technique: [0002] Chitin is the second largest naturally synthesized polymer material next to cellulose, and the annual output of this material by biosynthesis is as high as nearly one billion tons. However, due to the three-dimensional hydrogen bond structure in the chitin molecule, it has neither a specific melting point nor is it soluble in common solvents, which greatly limits it...

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): C08B37/08C08G81/00
Inventor 刘预田丰陈刚胡克鳌
Owner SHANGHAI JIAO TONG UNIV
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com