Use of lactide acid polymer
A technology based on polymers and lactic acid, which can be used in applications, food science, tobacco, etc., and can solve problems such as high breaking strength
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Embodiment 1
[0026] Under the protection of high-purity argon, add recrystallized 8kg L-lactide and 4.0g stannous octoate (Sn(Oct) 2 ), after 3 times of vacuum / argon gas treatment, the temperature was raised to 120°C, and the reaction was carried out under stirring for 24h, maintaining the positive pressure of the system. The temperature was raised from 120°C to 160°C, and the reaction was continued for 48h. Then slowly raise the temperature to 200°C, driven by the nitrogen pressure (8-5MPa) of the steel cylinder, discharge the material from the outlet of the lower part of the polymerization kettle, water-cool granulation, and dry. The viscosity-average molecular weight of this polymer is 62,000, the melt flow index is 23g / 10min, and the strength of bonding at room temperature with glyceryl triacetate (lapping area 10×3mm 2 ) is 4.2MPa. The melting point measured by DSC method is 171° C., and the degree of crystallinity is 40%.
[0027] The polymer is spun on a φ25×25 melt spinning mach...
Embodiment 2
[0029] The reaction conditions in Example 1 were adopted, but the lactide used was prepared from 80% L-lactic acid aqueous solution, and the method was as follows: 9 kg of 80% lactic acid aqueous solution was heated, evaporated and dehydrated. Add 30g of stannous octoate after no water evaporates, raise the temperature to 150°C, carry out condensation reaction for 4 hours, collect the generated water, and dehydrate under reduced pressure for 2 hours. After no water condenses, reduce the pressure to 0.001MPa, raise the temperature to 180°C, carry out thermal cracking reaction, collect the condensed product lactide (140-150°C), and gradually increase the reaction temperature to 240°C. Stop the reaction when there is very little distillate, distill the lactide on another distillation device, and collect the fraction at 160-170°C. Distilled three times. The lactide thus obtained underwent a racemization reaction, and an estimated 4% of L-lactic acid was converted to D-lactic acid...
Embodiment 3
[0032] Under the protection of high-purity argon, 4600 g of recrystallized L-lactide, 400 g of ε-caprolactone, 2.0 g of stannous octoate and 2 L of toluene were added to a degassed 10 L stainless steel polymerization kettle, and after 3 After vacuuming / argon gas treatment for the first time, the temperature was raised to 110°C, and the reaction was carried out for 24 hours under stirring. The positive pressure of the system was maintained, and the temperature was raised to 140°C to stop stirring, and the reaction was continued for 24 hours. Then slowly raise the temperature to 180°C, and under the drive of the cylinder nitrogen pressure (5-3MPa), discharge the material from the outlet of the lower part of the polymerization kettle, and water-cool granulation. The polymer was dissolved with 10 times the volume of toluene, and the polymer was precipitated with 5 times the volume of ethanol of the toluene solution, washed and centrifugally dried 3 times. Finally, the polymer is e...
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