Nano macromolecule microball of carboxy function type cross-linked nucleocapsid structure and preparation process thereof

A nano-polymer, core-shell structure technology, applied in the field of nano-polymer microspheres and its preparation, can solve the problems of poor solvent resistance and oil absorption, achieve the effect of enhancing interface compatibility, broadening application fields and application prospects

Inactive Publication Date: 2005-01-05
TSINGHUA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The purpose of the present invention is to provide a carboxyl-functional cross-linked core-shell nano-polymer microsphere and its preparation method. Both the core and the shell form a cross-linked structure, which not only solves the problem of preparing nanoscale core-shell latex particles, but also solves the problem of poor solvent resistance and oil absorption of the core-shell latex particles in the past; The surface of the ball introduces carboxyl functional groups that can react with a variety of polymer matrices and have ionization characteristics, making it widely used in the fields of polymer matrix filling modification, water purifier, catalyst, protein carrier, microcapsule embedding, etc. and exhibit various good properties

Method used

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  • Nano macromolecule microball of carboxy function type cross-linked nucleocapsid structure and preparation process thereof
  • Nano macromolecule microball of carboxy function type cross-linked nucleocapsid structure and preparation process thereof
  • Nano macromolecule microball of carboxy function type cross-linked nucleocapsid structure and preparation process thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0060] Example 1: 70 parts of styrene (St) as the core layer monoolefin monomer and 7 parts of divinylbenzene (DVB) as the core layer polyolefin monomer were mixed uniformly and set aside. Add 360 parts of deionized water, 6.5 parts of sodium dodecylsulfonate (SDS) and 0.5 part of nonylphenol polyoxyethylene ether into a four-necked bottle equipped with mechanical stirring, reflux condenser and thermometer, and raise the temperature to 50°C , add 30% of the previously prepared mixture to form a uniform emulsion. Then add 80% of the initiator aqueous solution made up of 0.5 parts of water-soluble initiator ammonium persulfate and 72 parts of deionized water, and raise the temperature to 82° C. for 30 minutes. Then the rest of the previously prepared mixture was added to the system, and the reaction was continued for 1 hour. Then add all the remaining initiator solution, and add 30 parts of butyl acrylate (BA) (as the shell monoolefin monomer) and 3 parts of divinylbenzene (DVB...

Embodiment 2

[0061] Example 2: 30 parts of butyl acrylate (BA) as the core layer monoolefin monomer and 3 parts of trimethylolpropane trimethacrylate (TM) as the core layer polyolefin monomer were mixed uniformly and set aside. Add 360 parts of deionized water, 4 parts of sodium dodecylsulfonate (SDS) and 0.5 part of nonylphenol polyoxyethylene ether into a four-necked bottle equipped with mechanical stirring, reflux condenser and thermometer, and raise the temperature to 50°C , add 70% of the previously prepared mixture to form a uniform emulsion. Then add 20% of the initiator aqueous solution made up of 0.5 parts of water-soluble initiator ammonium persulfate and 72 parts of deionized water, and raise the temperature to 70° C. for 2 hours. Then the temperature was raised to 82° C., and the rest of the previously prepared mixture was added to the system, and the reaction was continued for 1 hour. Then add all the remaining initiator solution, and add 70 parts of methyl methacrylate (MMA)...

Embodiment 3

[0062] Embodiment 3: Change methacrylic acid into 40 parts of oleic acid in Example 1, change the amount of sodium bicarbonate into 20 parts, increase the amount of initiator to 2 parts simultaneously, and the system temperature is 70 ℃, and the reaction time under each step Be respectively 2 hours, 3 hours, 3 hours, 3 hours, all the other formulas and steps are identical with embodiment 1. The performance index of the obtained product is shown in Table 1.

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Abstract

The invention is a carboxyl functional cross-linked core-shell nano high molecular microsphere and its preparing method, using multiple alkene monomers and alkene monomers with carboxyl functional groups as raw materials, on the condition of emulsifier, initiator and buffering agent, and preparing it by emulsion or suspension polymerization using water as medium; the product has a cross-linked structure inside both the core and shell, the core and shell are linked through chemical bonds, the carboxyl functional groups are grafted on the microsphere surface, and the particle size is less than 100 nm. By changing the composition of the core and shell, it obtains a nano high molecular microsphere with multiple different physico-chemical properties, and has very high freedom in selecting structure design. It solves the problem that the precious core-shell high molecular microshperes have no nano size and that the precious cores and shells are mostly linear polymers, and simultaneously by introducing ionizable and reactable carboxyl functional groups on the surface, and makes this microsphere have a completely wide application prospect in nano technical filed.

Description

technical field [0001] The invention relates to a carboxyl functional cross-linked core-shell nano-polymer microsphere and a preparation method thereof, belonging to the technical field of polymer materials. Background technique [0002] In recent years, the preparation of nano-polymer microspheres with core-shell structure has attracted more and more attention of researchers. This core-shell polymer microsphere not only has a nanoscale, but also can change the composition of the core and shell according to the needs, and obtain products with different physical and chemical properties, which has a high degree of freedom in design. [0003] The present inventors have successfully prepared cross-linked core-shell nano-polymer microspheres, and carried out surface epoxy functionalization on them, which solved the previous problem that the core-shell polymer microspheres do not have a nanoscale, and solved The core-shell polymer microspheres synthesized by the predecessors gene...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08F2/16C08F212/08C08F220/00
Inventor 于建曾重郭朝霞
Owner TSINGHUA UNIV
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