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A kind of isosorbide-based antibacterial self-healing polyurethane and its preparation method and application

An isosorbide, self-healing technology, applied in the field of polyurethane, achieves the effects of strong controllability of material properties, simple process, and increased environmental protection characteristics

Active Publication Date: 2022-03-04
宁波昌亚新材料科技股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

So far, there are no literature and patent reports on isosorbide-based polyurethanes with high-efficiency self-healing and antibacterial properties in the prior art

Method used

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  • A kind of isosorbide-based antibacterial self-healing polyurethane and its preparation method and application
  • A kind of isosorbide-based antibacterial self-healing polyurethane and its preparation method and application
  • A kind of isosorbide-based antibacterial self-healing polyurethane and its preparation method and application

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preparation example Construction

[0057] Another aspect of the embodiments of the present invention also provides a method for preparing the aforementioned isosorbide-based antibacterial self-healing polyurethane, which includes: in a protective atmosphere, making polydithiol, with isosorbide groups The chain extender, isocyanate, catalyst and organic solvent are reacted in a uniformly mixed reaction system to obtain the isosorbide-based antibacterial self-healing polyurethane.

[0058] In some more specific embodiments, the preparation method specifically includes:

[0059] In a protective atmosphere, uniformly mix polydithiol, chain extenders with isosorbide groups, isocyanates, catalysts, and organic solvents to form the uniformly mixed reaction system, and maintain the reaction in the uniformly mixed reaction system The concentration of the substance is 10-50wt%;

[0060] And, reacting the homogeneously mixed reaction system at 25-100° C. for 1-24 hours, and then post-processing to obtain the isosorbide-b...

Embodiment 1

[0076] In a glove box filled with 99.999% Ar, add fresh 1,5-pentanedithiol with 1,4-cyclohexanedimethanol divinyl ether to the reactor containing azobisisobutyronitrile and THF Carry out copolymerization, settle in methanol and wash several times, then carry out vacuum drying to obtain polydithiol with thioether bond and non-planar ring structure; then this polydithiol is mixed with isophorone diisocyanate, Dibutyltin, small molecule diol with isosorbide structure and tetrahydrofuran are poured into a three-neck reactor equipped with a mechanical stirrer for one-step reaction. Wherein, [polydithiol] / [small molecule diol with isosorbide structure]=1 / 99 (mass ratio), the number average molecular weight of polydithiol is 500g / mol, dibutyltin dilaurate accounts for the reaction 0.1wt% of the total mass of the substance, the molar ratio of ([hydroxyl group]+[thiol group]) to isocyanate group is 0.5:1, the concentration of all reactants is 10wt%, and the reaction temperature is 25°C...

Embodiment 2

[0085] In a glove box filled with 99.999% Ar, add fresh 1,5-pentanedithiol with 1,4-cyclohexanedimethanol divinyl ether to the reactor containing azobisisobutyronitrile and THF Copolymerize, settle in methanol and wash several times, then vacuum dry to obtain polydithiol with thioether bond and non-planar ring structure. Then pour this polydithiol, isophorone diisocyanate, dibutyltin dilaurate, small molecular diol with isosorbide structure and tetrahydrofuran into a three-neck reactor equipped with a mechanical stirrer for one-step reaction . Wherein, [polydithiol] / [small molecule diol with isosorbide structure]=50 / 50 (mass ratio), the number average molecular weight of polydithiol is 500g / mol, dibutyltin dilaurate accounts for the reaction 0.1wt% of the total mass of the substance, the molar ratio of ([hydroxyl group]+[thiol group]) to isocyanate group is 0.5:1, the concentration of all reactants is 10wt%, and the reaction temperature is 25°C. The time is 1h. Finally, the...

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Abstract

The invention discloses an isosorbide-based antibacterial self-healing polyurethane, a preparation method and application thereof. The isosorbide-based antibacterial self-healing polyurethane has a structure shown in the following formula: wherein, n is selected from 0-10, m is selected from 1-10, x is selected from 1-100, y is selected from 1-100, z is selected from 0 to 8, R 1 from C 1 -C 10 Any one or a combination of two or more of alkyl, alkenyl, and alkynyl. The isosorbide-based antibacterial self-healing polyurethane prepared by the invention has excellent mechanical properties, self-healing properties and antibacterial properties; at the same time, the preparation method provided by the invention has the advantages of simple process, easy-to-obtain raw materials, and strong controllability of material properties, etc. Features, has a very broad application prospects.

Description

technical field [0001] The invention belongs to the technical field of polyurethane, and in particular relates to an isosorbide-based antibacterial self-healing polyurethane and a preparation method and application thereof. Background technique [0002] Flexible electronics have broad application prospects in information, energy, medicine and other fields. Flexible electronics that can withstand deformations such as tension, compression, and bending have become a research hotspot in the fields of electronics, mechanics, materials, and physics. Flexible electronic devices are usually composed of several functional units, mainly including sensing units, circuits, and electrodes. Usually, the above-mentioned functional units are assembled on an elastomer matrix, and the matrix is ​​filled with one or more conductive fillers to obtain various functions. Since the elastic matrix determines the deformation capabilities (bending, stretching, and recovery) of flexible electronic d...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08G18/52C08G18/32C08G18/38A01N43/90A01P1/00A01P3/00
CPCC08G18/3218C08G18/52C08G18/3876A01N43/90
Inventor 徐建海王美兰
Owner 宁波昌亚新材料科技股份有限公司