Biodegradable block copolyester based on lactide-(alicyclic-co-aromatic)-lactide
A technology of block copolyester and lactide, which is applied in the field of biodegradable block copolyester, can solve the problems of less modified products, single topological structure, less active sites for chain extension, etc., and achieve a clear structure Effect
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[0044] A preparation method of biodegradable block copolyester, comprising the steps of:
[0045] (1) In the first reactor, alicyclic dibasic acid, aromatic dibasic acid and ethylene glycol undergo polycondensation reaction under the action of catalyst A to obtain the melt of A segment.
[0046](2) Transport the melt of segment A to the second reactor directly, and add lactide at the same time; under the action of catalyst B, lactide undergoes ring-opening polymerization on both sides of segment A to generate segment B , to obtain biodegradable block copolyesters.
[0047] In the synthesis of the A segment and the B segment, bulk polymerization is used.
[0048] The alicyclic dibasic acid is cis-1,4-cyclohexane dicarboxylic acid, trans-1,4-cyclohexane dicarboxylic acid, cis-1,3 cyclopentane dicarboxylic acid, trans- One or more of 1,3-cyclopentane dicarboxylic acid, cis-1,3-cyclobutane dicarboxylic acid, and trans-1,3-cyclobutane dicarboxylic acid. The aromatic dibasic acid...
Embodiment 1
[0052] (1) Synthesis of A segment
[0053] Transfer the equivalent of 0.1mol of trans-1,4-cyclohexanedicarboxylic acid, 0.9mol of terephthalic acid, and 1.1mol of ethylene glycol into the first reaction kettle and mix to obtain a slurry. Add the equivalent of 0.001mol antimony ethylene glycol, after esterification, polycondensate at 260°C and 50Pa for 1 hour to obtain the A segment.
[0054] (2) Synthesis of block copolyesters
[0055] Transfer the A segment to the second reaction kettle, add L-lactide with a mass of 100% of the A segment and stannous octoate with a molar weight of L-lactide of 0.05%, and open the ring at 200°C and 70Pa Polymerize for 4h to generate B segment and obtain block copolyester.
[0056] The copolyester can be completely degraded in 90 days under industrial composting environment.
Embodiment 2
[0058] (1) Synthesis of A segment
[0059] The equivalent of 0.1mol of cis-1,4-cyclohexanedicarboxylic acid, 0.2mol of trans-1,4-cyclohexanedicarboxylic acid, 0.7mol of furandicarboxylic acid, and 1.4mol of ethylene glycol were transported into the Mix in the first reaction kettle to obtain a slurry, add antimony trioxide equivalent to 0.005 mol, perform polycondensation at 265° C. and 30 Pa for 4 hours after esterification to obtain the A segment.
[0060] (2) Synthesis of block copolyesters
[0061] Transfer the A segment to the second reaction kettle, add D, L-lactide with a mass of 800% of the A segment and tin dichloride with a molar weight of D, L-lactide of 0.4%, at 180°C and 35Pa Ring-opening polymerization under the conditions of 20h to generate B segment and obtain block copolyester.
[0062] The copolyester can be completely degraded in 182 days under industrial composting environment.
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