A kind of recyclable self-healing thermosetting polymer and preparation method thereof
A thermosetting and polymer technology, applied in the field of self-healing thermosetting polymers and their preparation, can solve the problems of many reaction by-products, cumbersome preparation process, thermosetting polymers do not have self-healing properties, etc., and achieves easy polymerization and selectivity. The effect of wide and excellent recyclability
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Embodiment 1
[0041] A method for preparing a recyclable self-healing thermosetting polymer provided by a preferred embodiment of the present invention, the specific steps are as follows:
[0042] (1) 0.8g vinylbenzene boronic acid and 9.7g polyethylene glycol methacrylate were uniformly mixed in 35mL ethyl acetate, then 25mg initiator azobisisoheptonitrile was added, and stirred to obtain a mixed solution;
[0043] (2) The mixed solution was reacted in a water bath at 50°C for 12h under a nitrogen atmosphere;
[0044] (3) Pour the reacted solution into a mold (40mm×20mm×5mm) and dry it at 80°C for 24h, then place it in a vacuum drying oven at 70°C and heat until the solvent is completely evaporated.
Embodiment 2
[0046] A method for preparing a recyclable self-healing thermosetting polymer provided by a preferred embodiment of the present invention, the specific steps are as follows:
[0047] (1) uniformly mix 1.9g propenyl phenylboronic acid and 11.25g polyethylene glycol acrylate in 50mL ethanol, then add 40mg initiator azobisisobutyronitrile, and stir to obtain a mixed solution;
[0048] (2) The mixed solution was reacted in a water bath at 60°C for 18h under a nitrogen atmosphere;
[0049](3) Pour the reacted solution into a mold (40mm×20mm×5mm), and dry it at 70°C for 24h, then place it in a vacuum drying oven at 60°C and heat until the solvent evaporates completely.
Embodiment 3
[0051] A method for preparing a recyclable self-healing thermosetting polymer provided by a preferred embodiment of the present invention, the specific steps are as follows:
[0052] (1) Mix 3.4g of vinylbenzene boronic acid and 23.2g of polypropylene glycol acrylate in 55mL of N,N-dimethylethylenediamine uniformly, then add 80mg of initiator azobisisoheptonitrile, and stir to obtain a mixture solution;
[0053] (2) The mixed solution was reacted in a water bath at 55°C for 24h under a nitrogen atmosphere;
[0054] (3) Pour the reacted solution into a mold (40mm×20mm×5mm), and dry it at 100°C for 24h, then place it in a vacuum drying oven at 80°C and heat until the solvent evaporates completely.
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