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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

Pending Publication Date: 2021-12-07
ZHEJIANG HENGYI PETROCHEMICAL RES INST CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these modified copolyesters are usually random copolymers with a single topology. While the degradation performance is improved, the introduction of random aliphatic segments will reduce the mechanical strength of the material; on the other hand, the biological Less degradable modified products
[0005] CN 103570925A discloses a biodegradable polyester synthesized by adjusting the polyester composition. The polyester contains aliphatic, alicyclic, and aromatic segments, but its chain structure is random copolymerization, and the material stretches Intensity is low; CN105732964A discloses a kind of preparation method of dimer fatty acid polylactic acid block polyester, and the method for obtaining block structure is to further polymerize the aliphatic prepolymer and polylactic acid prepolymer under the action of a catalyst, This method has fewer polymerization active sites, and is easy to form a mixture of block polyester and two prepolymers; CN 101684175A discloses a biodegradable multi-block polyester copolymer, and its polyhydroxy acid segment is obtained by The prepolymer is further chain extended and connected to the aromatic polyester segment, which also has the problem of fewer active sites for chain extension

Method used

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Examples

Experimental program
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Effect test

preparation example Construction

[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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PUM

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Abstract

The invention relates to the field of high polymer materials, and discloses a biodegradable block copolyester based on lactide-(alicyclic-co-aromatic)-lactide. The structural formula of the biodegradable block copolyester is B-A-B, wherein A is an alicyclic-aromatic random copolyester chain segment, and the weight-average molecular weight of the alicyclic-aromatic random copolyester chain segment is 500-150,000 g / mol; B is a polylactide chain segment formed by polymerizing lactide in a ring opening manner, and the weight-average molecular weight of the polylactide chain segment is 500-200,000 g / mol; and the total weight average molecular weight of the block copolyester is 10,000-500,000 g / mol. The block copolyester is obtained by copolymerizing the alicyclic dibasic acid, the aromatic dibasic acid and the ethylene glycol and further performing ring opening on the lactide, the degradation property and the mechanical property of the copolyester are considered, and the block copolyester can be used as an environment-friendly material and a biomedical material.

Description

technical field [0001] The invention relates to the field of polymer materials, in particular to a biodegradable block copolyester based on lactide-(alicyclic-co-aromatic)-lactide. Background technique [0002] Synthetic polymers have unique mechanical and thermal properties due to their various chain compositions, chain structures, and aggregate structures. Its quality is stable and it can be used for a long time, which has greatly changed the production and life of human beings. Polyester is one of the most widely used synthetic polymers in the world, mainly polyethylene terephthalate (PET), which is non-toxic, transparent, stable in thermal and mechanical properties, and is therefore widely used in textiles , packaging, information, electronics and other fields. [0003] Although PET itself is non-toxic, it exists stably in nature for a long time. According to reports, the existence cycle of PET in the natural environment is at least 16-48 years, and bottle products ca...

Claims

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Application Information

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IPC IPC(8): C08G63/199C08G63/08C08G63/672C08G63/676
CPCC08G63/199C08G63/08C08G63/672C08G63/676C08G2230/00Y02W90/10
Inventor 李家旭王松林张德正吴海强欧阳杰赵志超王文俊
Owner ZHEJIANG HENGYI PETROCHEMICAL RES INST CO LTD
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