Technological method of catalytic synthesizing medical biodegradable material with biomass organic guanidine compound
A technology of biodegradable materials and process methods, applied in the fields of medical biodegradable materials, ring-opening polymerization of cyclic ester monomers, and synthesis of polyester polymers, can solve hidden dangers of safety, cytotoxicity, and removal of tin-containing catalysts And other issues
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Embodiment 1
[0018] In the reaction kettle, 144 grams of lactide were charged, and 119 mg of creatine was added according to monomer: catalyst=1000: 1 (molar ratio). Vacuumize the reactor, then replace it with nitrogen and repeat the operation three times, close the reactor under vacuum, heat the reactor slowly, and react at a constant temperature (150° C.) for a certain period of time for 72 hours. After stopping the reaction, the reactor was cooled to room temperature, and then acetone was added to dissolve the polymer in the reactor. Deionized water was then added to precipitate the polymer. The water phase was filtered off, and finally the precipitate was placed in a vacuum drying oven and dried under vacuum at 50° C. for 24 hours to obtain a white powdery solid with a yield of 97%. The polymer molecular weight is 1.0~2.0×10 4 , PDI≤1.40.
Embodiment 2
[0020] 144 grams of lactide were charged into the reactor, and 113 milligrams of creatinine was added according to monomer:catalyst=1000:1 (molar ratio). Vacuumize the reactor, then replace it with nitrogen and repeat the operation three times, close the reactor under vacuum, heat the reactor slowly, and react at a constant temperature (130° C.) for a certain period of time for 72 hours. After stopping the reaction, the reactor was cooled to room temperature, and then acetone was added to dissolve the polymer in the reactor. Deionized water was then added to precipitate the polymer. The water phase was filtered off, and finally the precipitate was placed in a vacuum drying oven and dried in vacuum at 50° C. for 24 hours to obtain a white powdery solid with a yield of 98.5%. The polymer molecular weight is 1.0~2.0×10 4 , PDI≤1.30.
Embodiment 3
[0022] In the reactor, 144 grams of lactide were charged, and 105 mg of guanidinoacetic acid was added according to monomer: catalyst=1000: 1 (molar ratio). Vacuumize the reactor, then replace it with nitrogen and repeat the operation three times, close the reactor under vacuum, heat the reactor slowly, and react at a constant temperature (150° C.) for a certain period of time for 72 hours. After stopping the reaction, the reactor was cooled to room temperature, and then acetone was added to dissolve the polymer in the reactor. Deionized water was then added to precipitate the polymer. The aqueous phase was filtered off, and finally the precipitate was placed in a vacuum drying oven and dried in vacuum at 50° C. for 24 hours to obtain a white powdery solid with a yield of 96.5%. The polymer molecular weight is 1.0~2.0×10 4 , PDI≤1.40.
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