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Force-induced responsive polymer with multi-hybrid network structure

A network structure and responsive technology, applied in the field of force-responsive polymers and their realization of force-responsive polymers, can solve the problem of inability to obtain self-healing properties, high stress/strain, poor material toughness, etc. question

Pending Publication Date: 2020-07-07
厦门天策材料科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] Polymer cross-linking is an important factor to obtain good mechanical strength and structural stability. The cross-linking effect includes physical cross-linking and chemical cross-linking. Traditional cross-linked polymer materials usually only contain a single cross-linked network structure, which in a certain However, for polymers that only contain physical crosslinks, the bonding is relatively weak and shows a certain degree of reversibility, which can increase the toughness, tear resistance, fatigue resistance and self-repair of the material. performance, etc., but it is precisely because of the reversibility of this cross-linked structure that it is easily affected by the external environment, such as acid resistance, alkali resistance, salt ion resistance, temperature resistance, etc., and cannot provide long-term stability.
Although traditional chemical cross-linked polymers can maintain high mechanical strength and long-term use stability, due to the strong bonding effect of their structure, the toughness of the material is poor, and silver cracks / microcracks are generated inside the material, which cannot effectively prevents it from expanding, and cannot achieve self-healing properties after damage to the material
In addition, traditional cross-linked polymer materials are not responsive to mechanical force, and can only be observed and detected when the mechanical force reaches the fracture threshold of the chemically connected structure and produces microcracks / cracks, which cannot be used for stress and deformation of the material. , damage and failure processes provide monitoring and warning functions, and cannot effectively repair structural damage
[0003] At present, most mechanoresponsive polymers require high stress / strain for mechanoresponse, and the mechanoresponse process can only occur after the material fails, which cannot really give full play to the effective early warning of material structure damage. The practical significance of improving the safety of materials is not great; and most mechanoresponsive polymers contain only one mechanoresponsive structural component, and the mechanoresponse effect is single, which also greatly limits its application

Method used

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  • Force-induced responsive polymer with multi-hybrid network structure
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  • Force-induced responsive polymer with multi-hybrid network structure

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Embodiment approach

[1924] In the present invention, the mechanoresponsive polymer may have one, two or more than two glass transition temperatures, or may not have a glass transition temperature. Among them, in a preferred embodiment of the present invention, at least one of the glass transition temperatures of the mechanoresponsive polymer is higher than 100°C, more preferably all of them are higher than 100°C, and the size of the resulting mechanoresponsive polymer Stability, mechanical strength, and high temperature resistance are good, and it is suitable for applications with high requirements for stress bearing and rigidity; in another preferred embodiment of the present invention, the glass transition temperature of the mechanically responsive polymer is at least One of them is between 25 and 100°C, more preferably all of them are between 25 and 100°C, which is convenient for preparing polymer products in the form of ordinary solids, foams, and gels above room temperature, and is suitable f...

Embodiment 1

[1942]

[1943] Take 5 molar equivalents of carboxyl double-terminated polyethylene glycol (molecular weight is 2000), 2.5 molar equivalents of compound (a), put them in a reaction vessel, dissolve them in tetrahydrofuran, add 10 molar equivalents of 1-ethyl-3-(3- Dimethylaminopropyl)-carbodiimide and 2.5 molar equivalents of 4-dimethylaminopyridine were stirred at room temperature for 24 hours to prepare cross-linked polyethylene glycol. Take 75 molar equivalents of polyethylene glycol monomethyl ether methacrylate, 15 molar equivalents of compound (b), 0.08 moles of single AIBN, 100 wt% cross-linked polyethylene glycol, fully swell with an appropriate amount of tetrahydrofuran, and pass through Nitrogen bubbling to remove oxygen for 30 minutes, then raise the temperature to 65°C under a nitrogen atmosphere, stir and react for 24 hours, and then purify and dry to obtain a double-network polymer; then swell the purified product in a large amount of distilled water, and after...

Embodiment 2

[1945]

[1946]Take 3 moles of a single amount of hydroxyl-terminated four-armed polyethylene glycol (molecular weight is 1200), 6 molar equivalents of compound (a), put them in a reaction vessel, dissolve them in tetrahydrofuran, add 12 molar equivalents of 1-ethyl-3-( 3-Dimethylaminopropyl)-carbodiimide and 3 molar equivalents of 4-dimethylaminopyridine were stirred at room temperature for 24 hours to prepare cross-linked polyethylene glycol. With stannous octoate as a catalyst, polyethylene glycol (molecular weight is 1000) and 10 times excess hexamethylene diisocyanate is reacted by hydroxyl-terminated polyethylene glycol to prepare isocyanate group double-terminated polyethylene glycol; get 20g cross-linked Polyethylene glycol is placed in a reaction vessel, swelled with an appropriate amount of ethanol, then 0.01 molar equivalent of isocyanate group-dicapped polyethylene glycol is added, stirred and mixed for 15 minutes, and then 0.01 molar equivalent of carbohydrazide...

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Abstract

The invention discloses a force-induced responsive polymer with a multi-hybrid network structure. The force-induced responsive polymer contains at least two cross-linked networks and also contains non-dynamic covalent bond covalent cross-linking and non-covalent cross-linking at the same time, and the cross-linking degree of the non-dynamic covalent bond covalent cross-linking in at least one cross-linked network is above a gel point; wherein the cross-linked network contains at least one force-sensitive group; under the action of mechanical force, the force-sensitive group is subjected to chemical and / or physical changes, and force-induced response is achieved. The multi-hybrid network structure provides excellent structural stability and mechanical properties for the polymer; based on the force-induced responsiveness of the force-sensitive group, the monitoring and warning effects on the stress, deformation, damage and failure processes are obtained; and non-covalent dynamics may provide self-repairing performance. The force-induced responsive polymer can be applied to a stress sensing material, a self-repairing material, a tough material, a shape memory material, a toy material,a functional coating material, an intelligent sensor, a binding material, a plugging material and the like.

Description

technical field [0001] The present invention relates to a mechanoresponsive polymer and a method for realizing the mechanoresponse, in particular to a mechanoresponsive polymer having a heterogeneous network structure and containing at least one mechanosensitive group and realizing the mechanoresponse A Mechanotropic Response Approach for Responsive Polymers. Background technique [0002] Polymer cross-linking is an important factor to obtain good mechanical strength and structural stability. The cross-linking effect includes physical cross-linking and chemical cross-linking. Traditional cross-linked polymer materials usually only contain a single cross-linked network structure, which in a certain However, for polymers that only contain physical crosslinks, the bonding is relatively weak and shows a certain degree of reversibility, which can increase the toughness, tear resistance, fatigue resistance and self-repair of the material. performance, etc., but it is precisely be...

Claims

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Application Information

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IPC IPC(8): C08J3/24C08G83/00
CPCC08J3/24C08G83/008
Inventor 不公告发明人
Owner 厦门天策材料科技有限公司
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