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A kind of preparation method of high specific surface area chitosan microsphere

A technology of chitosan microspheres and high specific surface area, applied in the field of materials, can solve the problems of low specific surface area, limited functionalization of chitosan, reduction of specific surface area, etc.

Active Publication Date: 2021-09-14
SICHUAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the currently existing chitosan microspheres generally have the disadvantage of low specific surface area, which is mainly due to the high crystallinity of chitosan fibers caused by internal strong hydrogen bonds, resulting in a decrease in specific surface area.
This high crystallinity results in a large number of hydroxyl and amino groups buried in the crystalline region, which greatly limits the further functionalization of chitosan.

Method used

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  • A kind of preparation method of high specific surface area chitosan microsphere

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Experimental program
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Embodiment 1

[0026] 4g chitosan powder was mixed with alkali urea solution (4.5wt% LiOH / 7wt% KOH / 8wt% urea) for 5min; the above solution was placed in a refrigerator at -25°C for 5h, then mechanically stirred and thawed at 300rpm, and thawed This solution is placed in-25 ℃ of refrigerator again afterwards again, repeat above-mentioned operation 3 times, form the chitosan solution that concentration is 4wt%; Adopt similar method, agarose powder and alkali urea solution (4wt%LiOH / 16wt% urea) mixed 5min, after freezing-thawing process, obtain the agarose solution of 3wt%; The above-mentioned obtained chitosan solution and agarose solution are mixed 2h with the volume ratio of 85:15, obtain uniform chitosan / agar Sugar mixed solution, take 10mL of this solution as the dispersed phase, use 100mL of isooctane as the oil phase, add 3g of surfactant Span80, and emulsify for 2h to obtain a chitosan / agarose emulsion; add 100mL of absolute ethanol to the above emulsion , to obtain regenerated chitosan...

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Abstract

The invention relates to a novel method for preparing chitosan microspheres with a high specific surface area, belonging to the technical field of materials. The preparation method is to uniformly mix chitosan solution and agarose solution in advance, and obtain chitosan / agarose composite microspheres through emulsification and regeneration processes, and then remove agarose by heat treatment to obtain chitosan with high specific surface area Microspheres. The results show that the specific surface area of ​​chitosan microspheres prepared by this preparation method is significantly improved. At the same time, the present invention uses agarose as a pore-forming agent, which is low in cost, has no pollution to the environment, is easy to degrade, and does not cause the collapse of the pore structure. scope of application.

Description

technical field [0001] The invention belongs to the technical field of materials and relates to a method for preparing chitosan microspheres with high specific surface area. Background technique [0002] Chitosan is the only alkaline polysaccharide that exists in nature. Its molecular structure is 2-acetylamino-2-deoxy-D-glucopyranose and 2-amino-2-deoxy-D-glucopyranose connected by glycosidic bonds. polymer. Commercial chitosan is mainly obtained from raw materials rich in chitin, such as shrimp and crab, after deacetylation treatment. Generally, chitin with a degree of deacetylation greater than 50% is called chitosan. Chitosan has unique physical and chemical properties, such as cationic polyelectrolyte, antibacterial, non-toxic and biocompatibility. At the same time, due to its rich hydroxyl and amino groups, chitosan-based materials with different functions can be obtained by reacting with other functional monomers or hybridization, which shows great application pote...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08J9/26C08L5/08
CPCC08J9/26C08J2201/0464C08J2305/08C08J2405/12
Inventor 杜开峰乔亮智
Owner SICHUAN UNIV