Method for preparing degradable copolyester by trinary reactivity blending
A reactive and copolyester technology, which is applied in the field of ternary reactive blending to prepare degradable copolyesters. It can solve the problems of high price, limited application range of materials, poor mechanical and thermal properties, etc., and increase the molecular weight of polymers. , easy reaction operation and simple synthesis process
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Embodiment 1
[0008] Example 1 Add a certain proportion of 0.1 mmol D,L-oligolactic acid and 91.9 mmol polyethylene glycol in a nitrogen bottle, heat at 100°C for 2 hours, then raise the temperature to 200°C, keep for 2 hours, and keep at 200°C, Vacuuming for 2 h gave the reactive blend required for the experiment. Add 8 mmol polybutylene terephthalate, oligomeric lactic acid and polyethylene glycol copolymer into the flame-dried three-necked flask. The reaction was heated to 110°C, during the heating process, a vacuum was drawn for a period of time, and then N 2 , This process is repeated 5-6 times. Pass N at 110°C 2 , keep for 1 hour. Then heated to 260°C, vacuumed, and the reaction was maintained for 1.5 hours. Stop heating, cool down after the reaction stops, add to chloroform solution to dissolve, and then pour the solution into a large amount of methanol to obtain a white polymer precipitate. The filtrate was dried under vacuum at 40°C.
Embodiment 2
[0009] Example 2 Add a certain proportion of 29.9 mmol D,L-oligolactic acid and 0.1 mmol polyethylene glycol in a nitrogen bottle, heat at 100°C for 2 hours, then raise the temperature to 200°C, keep for 2 hours, and keep at 200°C, Vacuuming for 2 h gave the reactive blend required for the experiment. Add 70 mmol polybutylene terephthalate, oligomeric lactic acid and polyethylene glycol copolymer into the flame-dried three-necked bottle. The reaction was heated to 110°C, during the heating process, a vacuum was drawn for a period of time, and then N 2 , This process is repeated 5-6 times. Pass N at 110°C 2 , keep for 1 hour. Then heated to 260°C, vacuumed, and the reaction was maintained for 1.5 hours. Stop heating, cool down after the reaction stops, add to chloroform solution to dissolve, and then pour the solution into a large amount of methanol to obtain a white polymer precipitate. The filtrate was dried under vacuum at 40°C.
[0010] Result analysis
[0011] Copol...
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