Aliphatic-aromatic copolyester, preparation method and application thereof

An aromatic and copolyester technology, applied in the direction of adhesives, etc., can solve the problems of easy aging, easy hydrolysis, low melting point, etc.

Active Publication Date: 2010-06-02
HANGZHOU XINFU TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are some disadvantages in the application of aliphatic polyester, such as relatively expensive price, relatively low melting point, rela

Method used

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  • Aliphatic-aromatic copolyester, preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] Add 1000ml of chloroform, 507.5 grams of terephthaloyl chloride and 387.5 grams of succinoyl chloride in the reaction flask, stir well, add dropwise a mixture of 450 grams of butanediol and 11.6 grams of monoethylene glycol acrylate under stirring, and control the reaction temperature at 0~40°C, after the dropwise addition is completed, continue to stir for 60 minutes to complete the reaction. The hydrogen chloride produced in the reaction was absorbed with NaOH solution.

[0050] After the reaction is complete, distill off the chloroform, add 0.5-1 g of tetrabutyl titanate, stir thoroughly for 20 minutes after melting, fill the bottle with nitrogen to replace the air in the bottle, reduce the pressure to 100-1000 Pa, continue to heat up to 180-250 °C, and stir After reacting for 60-120 minutes, light yellow to white polymer 1 was obtained. The GPC method determined that the molecular weight was 65,300 for Mn, 140,400 for Mw, and the molecular weight distribution was 2...

Embodiment 2

[0052] Add 1000ml of chloroform, 507.5 grams of terephthaloyl chloride, 387.5 grams of succinoyl chloride and 4.5 grams of acryloyl chloride into the reaction flask and stir evenly, then add dropwise 62 grams of ethylene glycol, 270 grams of butanediol, 95 grams of hexanediol, Mixture of 80 grams of polyethylene glycol, control reaction temperature at 0~40 ℃, dropwise, continue to stir for 60 minutes to make reaction complete. The hydrogen chloride produced in the reaction was absorbed with NaOH solution.

[0053] After the reaction is complete, distill off the chloroform, add 0.5-1 g of tetrabutyl titanate, stir for 20 minutes, fill the bottle with nitrogen to replace the air in the bottle, reduce the pressure to 100-1000 Pa, continue to heat up to 180-250 ° C, and react for 60-120 minutes , to obtain light yellow to white polymer 2. The GPC method determined that the molecular weight was 58,200 for Mn, 134,500 for Mw, and a molecular weight distribution of 2.31.

Embodiment 3

[0055] Add 1000ml of chloroform, 507.5g of terephthaloyl chloride, 457.5g of adipoyl chloride and 4.5g of acryloyl chloride into the reaction bottle, stir evenly, add dropwise a mixture of 441g of butanediol and 100g of polyethylene glycol under stirring to control the reaction The temperature is 0-40°C, after the dropwise addition is completed, the stirring is continued for 60 minutes to complete the reaction. The hydrogen chloride produced in the reaction was absorbed with NaOH solution.

[0056] After the reaction is complete, distill off the chloroform, add 0.5-1 g of tetrabutyl titanate, stir thoroughly for 20 minutes after melting, fill the bottle with nitrogen to replace the air in the bottle, reduce the pressure to 100-1000 Pa, continue to heat up to 180-250 °C, and stir After 60-120 minutes of reaction, polymer 3 was obtained. The GPC method determined that the molecular weight was 49,600 for Mn, 137,900 for Mw, and the molecular weight distribution was 2.78.

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Abstract

The invention provides aliphatic-aromatic copolyester, a preparation method and application thereof. Polymerization monomers comprise a compound selected from aliphatic dibasic acid, and naphthenic base dibasic acid or the ester, the anhydride and the acyl halide thereof, a compound selected from aromatic dibasic acid or the ester, the anhydride and the acyl halide thereof, a compound simultaneously with two functional groups selected from an amino-group, a mercapto group or a hydroxy or a compound of a derivative of the amino-group, the mercapto group or the hydroxyl with an epoxy group and an azepine ring, a compound selected from unsaturated acid with at least one C-C, C-O, C-N or C-S double bond and C-C or C-N triple bond or the ester, the anhydride and the acyl halide thereof and a compound of unsaturated alcohol with at least one C-C double bond or a C-C triple bond or an epoxide thereof. The aliphatic-aromatic copolyester is prepared by carrying out esterification and polycondensation after mixing the polymerization monomers, polymerizing the double bonds and/or the triple bonds on the polymerization monomers under the action of an initiator and then carrying out a graftingand/or coupling reaction.

Description

technical field [0001] The invention relates to an aliphatic-aromatic copolyester and its preparation method and application, in particular to a high molecular weight, biodegradable aliphatic-aromatic copolyester and its preparation method and application. Background technique [0002] At present, polymer materials have penetrated into various fields of people's lives. While it brings convenience to people, it also creates a problem to be solved-"white pollution". Most of the polymer materials currently used cannot be degraded in the environment for a long time, and a large amount of them remain in the environment after use. The pressure on the environment is increasing year by year, destroying the ecological environment of the earth and affecting the recycling of resources. As people are concerned about their living environment, more and more people pay attention to environmentally friendly biodegradable polymer materials. [0003] There are ester bonds in the main molecul...

Claims

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Application Information

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IPC IPC(8): C08G63/54C08G63/676C08L67/06C09J167/06
CPCC08G63/21C08G63/47C08F299/04
Inventor 戴清文姜凯林关羽过鑫富白彦兵王康刘兆涛孙小峰
Owner HANGZHOU XINFU TECH CO LTD
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