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
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[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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