CN112480361A - Preparation method of moisture-permeable thermoplastic polyurethane film - Google Patents

Preparation method of moisture-permeable thermoplastic polyurethane film Download PDF

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CN112480361A
CN112480361A CN202011384274.7A CN202011384274A CN112480361A CN 112480361 A CN112480361 A CN 112480361A CN 202011384274 A CN202011384274 A CN 202011384274A CN 112480361 A CN112480361 A CN 112480361A
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thermoplastic polyurethane
film
moisture
diisocyanate
polyurethane film
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CN112480361B (en
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贾润萍
刘宝全
任静宇
史继超
郜峰
杨朴
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Shanghai Hiend Polyurethane Inc
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Shanghai Hiend Polyurethane Inc
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
    • C08G18/753Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
    • C08G18/755Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4244Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups
    • C08G18/4247Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids
    • C08G18/4252Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids derived from polyols containing polyether groups and polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6633Compounds of group C08G18/42
    • C08G18/6637Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/664Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/66Polyesters containing oxygen in the form of ether groups
    • C08G63/668Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes
    • C08J2375/06Polyurethanes from polyesters

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

The invention belongs to the field of preparation of thermoplastic polyurethane films, and particularly relates to a preparation method of a moisture-permeable thermoplastic polyurethane film. Reacting citric acid with dihydric alcohol, adding gallic acid, and adding a catalyst to react to obtain hyperbranched polyester polyol with a large number of hydrophilic groups; the hyperbranched polyester polyol is reacted with diisocyanate and a micromolecular chain extender, and the thickness, the forming temperature and the relative temperature of the film are adjusted through a film blowing forming process to prepare the thermoplastic polyurethane film with a pore-free mode and good moisture permeability. The hyperbranched polyester polyol prepared by the invention has high branching degree, the tail end of the hyperbranched polyester polyol has a large number of hydrophilic groups, and a more economic blow molding process is adopted, so that the synthesis process is simple. The thermoplastic polyurethane film prepared by the process has good hydrophilicity, mechanical property and moisture permeability, and has application value in the fields of medical supplies, clothes, home furnishing, food packaging and the like.

Description

Preparation method of moisture-permeable thermoplastic polyurethane film
The technical field is as follows:
the invention belongs to the field of preparation of thermoplastic polyurethane films, and particularly relates to a preparation method of a moisture-permeable thermoplastic polyurethane film.
Background art:
thermoplastic polyurethane film (TPU film for short) is an elastic block copolymer which is mainly made of diisocyanate or polyester/polyether diol and consists of a flexible soft segment area and a rigid functional group hard segment area. The special chemical structure not only endows the material with excellent mechanical property and wear resistance, but also has the advantages of good toughness, oil resistance, corrosion resistance and the like, is a mature environment-friendly material, and is widely applied to the fields of medical products, clothes, home decoration, building materials, food packaging and the like. Although the TPU film has good waterproof performance, the TPU film usually has poor permeability to oxygen, water vapor and other small molecular substances, in order to improve the hydrophilicity and moisture permeability of the TPU film, researches are mostly carried out by introducing hydrophilic polyester/polyether diol and chemical bonding hydrophilic functional groups singly or preparing microporous or non-porous TPU films by physical techniques such as electrostatic spinning and air spinning, and the like. Therefore, by improving the chemical structure of the TPU, the TPU film has more hydrophilic groups to improve the hydrophilic moisture permeability, and a certain forming process is adopted to prepare the TPU film with no holes, good moisture permeability and uniform thickness, so that the comprehensive performance of the TPU film can be improved and the application field of the TPU film can be enlarged.
With the improvement of living standard of people, certain requirements are required on the waterproofness and the air permeability of materials in the industries of clothes, outdoor articles, medical supplies and the like. The hyperbranched polyester polyol has the characteristics of high branching, a large number of terminal functional groups, ordered structure, monodispersity and the like, and meanwhile, the hyperbranched polyester polyol is simple in synthesis process and has lower viscosity and good fluidity compared with the common polyester polyol. The hyperbranched polyester polyol tail segment has a large number of hydrophilic groups, and is used as a raw material to prepare a TPU film, so that the hydrophilic moisture permeability of the film can be improved to a great extent, and the film is processed into a waterproof and high-moisture-permeability pore-free film through a film coating, film blowing or rolling mode, and the like, so that the film can be applied to various industries.
Therefore, the invention discloses a hydrophilic TPU film prepared from hyperbranched polyester polyol with a large number of hydrophilic groups, and the TPU film with a pore-free shape and good moisture permeability is prepared by a certain forming technology, so that the invention has a good application prospect.
The invention content is as follows:
the invention aims at the problems and provides a preparation method of a moisture-permeable thermoplastic polyurethane film.
In order to achieve the purpose, the invention adopts the following technical scheme that the preparation method comprises the following specific steps,
1. preparation of hyperbranched polyester polyols
Putting 10-30 parts by weight of citric acid and 5-40 parts by weight of dihydric alcohol into a three-neck round-bottom flask, heating to 100-150 ℃, introducing nitrogen, and stirring for 1-2 hours; adding 30-100 parts by weight of gallic acid, stirring at 120-150 ℃ for 0.5-2 h, adding 0.2-1 part by weight of catalyst, continuing stirring for 0.5-2 h, vacuumizing the reaction system for about 5min at intervals of 0.5h to remove small molecular byproducts, and stopping the reaction until the weight of the reaction system is not obviously changed to obtain hyperbranched polyester polyol;
2. preparation of hydrophilic thermoplastic polyurethanes
Respectively removing water for 1-2 hours at 50-70 ℃ in vacuum by using 30-60 parts by weight of diisocyanate and 15-30 parts by weight of micromolecular chain extender; adding 30-60 parts by weight of the hyperbranched polyester polyol prepared in the step 1 into a three-neck flask provided with a stirring device, heating to 100-130 ℃, vacuumizing and dehydrating for 0.5-2 h, cooling to 80-100 ℃, adding molten and dehydrated diisocyanate, stirring for 1-2 h, continuously adding the dehydrated micromolecule chain extender, and stirring for 1-2 h at 70-100 ℃ to obtain the hydrophilic thermoplastic polyurethane;
3. preparation of moisture-permeable thermoplastic polyurethane film
And (3) quickly pouring the product obtained in the step (2) into a film blowing machine for melt blending, setting the blowing width, the blowing thickness and the three-section temperature of a machine head of the film blowing machine set according to requirements for film blowing, finally, cooling and shaping the film by using a cooling machine, and drying the obtained thermoplastic polyurethane film at the temperature of 20-45 ℃ for 0.2-2.0 h to obtain the moisture-permeable thermoplastic polyurethane film.
Preferably, the diol in step 1 is one or more of ethylene glycol, propylene glycol, diethylene glycol ethyl ether, polytetrahydrofuran glycol, polyethylene glycol 200, polyethylene glycol 600 and polypropylene glycol.
Preferably, the catalyst in step 1 is one or more of sodium bisulfate, p-toluenesulfonic acid, concentrated sulfuric acid, concentrated hydrochloric acid and thionyl chloride.
Preferably, the diisocyanate in step 2 is one or more of diphenylmethane diisocyanate, toluene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, 1, 5-naphthalene diisocyanate, p-phenylene diisocyanate, dimethyl biphenyl diisocyanate, and hexamethylene diisocyanate;
preferably, the small molecule chain extender in step 2 is one or more of ethylene glycol, 1, 2-propylene glycol, 1, 3-propylene glycol, 1, 4-butanediol, 1, 6-hexanediol, cyclohexane dimethanol, diethylene glycol, glycerol, ethylenediamine, triethanolamine, triisopropanolamine, diethyl toluene diamine, and N-methyl diethanolamine;
preferably, in the step 3, the width of the blown film is 150 cm-160 cm, the thickness of the blown film is 0.2 mm-0.5 mm, and the temperature interval of the three sections of the head of the film blowing unit is 155-175 ℃.
The invention has the beneficial effects that:
1. the invention introduces two biological raw materials of citric acid and gallic acid to prepare the hyperbranched polyester polyol, and the preparation process has no use of organic solvent and simple operation. The gallic acid and citric acid are sustainable biological resources and have low cost, and the molecular structure has a terminal polyhydroxy and carboxyl branched structure. The prepared hyperbranched polyester polyol is environment-friendly hyperbranched polyester polyol, has high branching degree, has a large number of hydrophilic groups at the tail end, and has good hydrophilicity.
2. The invention provides a hyperbranched polyester polyol synthesized moisture permeable thermoplastic polyurethane film and a preparation method thereof, and the hyperbranched polyester polyol synthesized moisture permeable thermoplastic polyurethane film has the advantages of simple production process and low cost and is suitable for industrial production. Compared with a microporous film, the microporous film has the advantages of better wind resistance and water resistance, microorganism isolation, no influence of dust and the like. Compared with the casting and extrusion film forming processes, the blow molding process is more economical, the blow-up ratio is easy to control, and the controllable range of the film thickness is large. Hydrophilic films are sensitive to temperature and humidity, and their moisture permeability depends on the thickness of the film and its chemical structure and degree of crosslinking. The hyperbranched polyester polyol is introduced to change the chemical structure of the TPU, and the thickness and the forming temperature of the film are adjusted to prepare the TPU film with uniform thickness, no pore and good moisture permeability.
The specific implementation mode is as follows:
the raw materials used in the examples were purchased from the research platform.
The water contact angle was measured by a contact angle measuring instrument (A801S, KINO Industry Co., U.S.A.); a universal material testing machine (SUN500, Italy Cardano ALCamp company) is adopted to carry out mechanical property test according to GB/T1040-; the moisture permeability was measured by a YG601H type computerized moisture permeability tester according to American Standard (ASTME96 BW-2000).
Example 1
1kg of citric acid and 2.5kg of polyethylene glycol 200 by weight are placed in a three-necked round-bottomed flask equipped with a nitrogen inlet, a thermometer and a mechanical stirrer, heated to 140 ℃, introduced with nitrogen and stirred for 2 hours; adding 3kg of gallic acid, stirring at 120 ℃ for 2h, adding 0.05kg of p-toluenesulfonic acid, continuously stirring for 1.5h, vacuumizing the reaction system for about 5min at intervals of 0.5h to remove small molecular by-products, and stopping the reaction until the weight of the reaction system is not obviously changed to obtain the hyperbranched polyester polyol;
firstly, respectively removing water in vacuum for 1h at 60 ℃ by 3kg of isophorone diisocyanate and 1.5kg of 1, 4-butanediol; adding 3kg of prepared hyperbranched polyester polyol into a three-neck flask provided with a stirring device, heating to 120 ℃, vacuumizing and dehydrating for 1.5h, cooling to 80 ℃, adding molten and dehydrated isophorone diisocyanate, stirring for 1h, continuously adding dehydrated 1, 4-butanediol, and stirring for 1h at 80 ℃ to obtain the hydrophilic thermoplastic polyurethane;
and (2) quickly pouring the product into a die head of a blow molding machine, processing the product by using the blow molding machine (the blowing ratio is set to be 2.5, the traction speed is set to be 30m/min), blowing the product with the width of 155cm, the temperature of three sections of a machine head is 155 ℃, 160 ℃ and 165 ℃, adjusting the thickness of the film by using the die head to be 0.2mm, finally cooling and shaping the film by using a cooling machine, and drying the obtained thermoplastic polyurethane film at the temperature of 45 ℃ for 1.0h to obtain the moisture-permeable thermoplastic polyurethane film.
The water contact angle of the moisture-permeable thermoplastic polyurethane film is 31.5 degrees through detection; tensile strength of 37.2Mpa, elongation at break of 489%; the moisture permeability is 11046g/(m2 & 24h) under the conditions that the temperature is 35 ℃ and the relative humidity is 50 percent.
Example 2
Placing 1.5kg of citric acid and 3kg of polyethylene glycol 200 in parts by weight in a three-necked round-bottomed flask equipped with a nitrogen inlet, a thermometer and a mechanical stirrer, heating to 140 ℃, introducing nitrogen, and stirring for 2 hours; adding 3kg of gallic acid, stirring at 120 ℃ for 2h, adding 0.05kg of p-toluenesulfonic acid, continuously stirring for 1.5h, vacuumizing the reaction system for about 5min at intervals of 0.5h to remove small molecular by-products, and stopping the reaction until the weight of the reaction system is not obviously changed to obtain the hyperbranched polyester polyol;
firstly, respectively removing water in vacuum for 1h at 60 ℃ by 3kg of isophorone diisocyanate and 1.5kg of 1, 4-butanediol; adding 3kg of prepared hyperbranched polyester polyol into a three-neck flask provided with a stirring device, heating to 120 ℃, vacuumizing and dehydrating for 1.5h, cooling to 80 ℃, adding molten and dehydrated isophorone diisocyanate, stirring for 1h, continuously adding dehydrated 1, 4-butanediol, and stirring for 1h at 80 ℃ to obtain the hydrophilic thermoplastic polyurethane;
quickly pouring the product into a die head of a blow molding machine, processing the product by using the blow molding machine (the blow-up ratio is set to be 2.5, the traction speed is set to be 32m/min), blowing the product with the width of 153cm, adjusting the thickness of the film by using the die head to be 0.25mm, finally cooling and shaping the film by using a cooling machine, and drying the obtained thermoplastic polyurethane film for 1.5 hours at the temperature of 35 ℃ to obtain the moisture-permeable thermoplastic polyurethane film;
the water contact angle of the moisture-permeable thermoplastic polyurethane film is 33.8 degrees through detection; the tensile strength is 34.4Mpa, the elongation at break is 463%; under the conditions that the temperature is 35 ℃ and the relative humidity is 50%, the moisture permeability is 10923g/(m2 & 24 h).
Example 3
Placing 1.5kg of citric acid and 3.5kg of polyethylene glycol 200 into a three-necked round bottom flask equipped with a nitrogen inlet, a thermometer and a mechanical stirrer, heating to 140 ℃, introducing nitrogen, and stirring for 2 hours; adding 3kg of gallic acid, stirring at 120 ℃ for 2h, adding 0.05kg of p-toluenesulfonic acid, continuously stirring for 1.5h, vacuumizing the reaction system for about 5min at intervals of 0.5h to remove small molecular by-products, and stopping the reaction until the weight of the reaction system is not obviously changed to obtain the hyperbranched polyester polyol;
firstly, respectively removing water in vacuum for 1h at 60 ℃ by 3kg of isophorone diisocyanate and 1.5kg of 1, 4-butanediol; adding 3kg of prepared hyperbranched polyester polyol into a three-neck flask provided with a stirring device, heating to 120 ℃, vacuumizing and dehydrating for 1.5h, cooling to 80 ℃, adding molten and dehydrated isophorone diisocyanate, stirring for 1h, continuously adding dehydrated 1, 4-butanediol, and stirring for 1h at 80 ℃ to obtain the hydrophilic thermoplastic polyurethane;
and (2) quickly pouring the product into a die head of a blow molding machine, processing the product by using the blow molding machine (the blowing-up ratio is set to be 2.5, the traction speed is set to be 30m/min), blowing the product with the width of 158cm, the temperature of three sections of the machine head is 165 ℃, 170 ℃ and 175 ℃, adjusting the thickness of the film by using the die head to be 0.3mm, finally cooling and shaping the film by using a cooling machine, and drying the obtained thermoplastic polyurethane film at the temperature of 30 ℃ for 2.0h to obtain the moisture-permeable thermoplastic polyurethane film.
The water contact angle of the moisture-permeable thermoplastic polyurethane film is 35.9 degrees through detection; the tensile strength is 31.7Mpa, and the elongation at break is 455%; the moisture permeability is 10558g/(m 2h 24h) under the conditions that the temperature is 35 ℃ and the relative humidity is 50%.
The above description is only a basic description of the present invention, and any equivalent changes made according to the technical solution of the present invention should fall within the protection scope of the present invention.

Claims (6)

1. A preparation method of a moisture permeable thermoplastic polyurethane film is characterized by comprising the following specific preparation steps,
(1) preparation of hyperbranched polyester polyols
Putting 10-30 parts by weight of citric acid and 5-40 parts by weight of dihydric alcohol into a three-neck round-bottom flask, heating to 100-150 ℃, introducing nitrogen, and stirring for 1-2 hours; adding 30-100 parts by weight of gallic acid, stirring at 120-150 ℃ for 0.5-2 h, adding 0.2-1 part by weight of catalyst, continuing stirring for 0.5-2 h, vacuumizing the reaction system for about 5min at intervals of 0.5h to remove small molecular byproducts, and stopping the reaction until the weight of the reaction system is not obviously changed to obtain hyperbranched polyester polyol;
(2) preparation of hydrophilic thermoplastic polyurethanes
Respectively removing water for 1-2 hours at 50-70 ℃ in vacuum by using 30-60 parts by weight of diisocyanate and 15-30 parts by weight of micromolecular chain extender; adding 30-60 parts by weight of the hyperbranched polyester polyol prepared in the step 1) into a three-neck flask provided with a stirring device, heating to 100-130 ℃, vacuumizing and dehydrating for 0.5-2 h, cooling to 80-100 ℃, adding molten and dehydrated diisocyanate, stirring for 1-2 h, continuously adding the dehydrated micromolecule chain extender, and stirring for 1-2 h at 70-100 ℃ to obtain the hydrophilic thermoplastic polyurethane;
(3) preparation of moisture-permeable thermoplastic polyurethane film
And (3) quickly pouring the product obtained in the step 2) into a film blowing machine for melt blending, setting the blowing width and thickness and the three-section temperature of a machine head of the film blowing machine set according to requirements for film blowing, finally, cooling and shaping the film by using a cooling machine, and drying the obtained thermoplastic polyurethane film at the temperature of 20-45 ℃ for 0.2-2.0 h to obtain the moisture-permeable thermoplastic polyurethane film.
2. The method for preparing the moisture-permeable thermoplastic polyurethane film according to claim 1, wherein the glycol in the step 1) is one or more of ethylene glycol, propylene glycol, diethylene glycol ethyl ether, polytetrahydrofuran glycol, polyethylene glycol 200, polyethylene glycol 600 and polypropylene glycol.
3. The method for preparing the moisture-permeable thermoplastic polyurethane film according to claim 1, wherein the catalyst in the step 1) is one or more of sodium bisulfate, p-toluenesulfonic acid, concentrated sulfuric acid, concentrated hydrochloric acid and thionyl chloride.
4. The method for preparing the moisture-permeable thermoplastic polyurethane film according to claim 1, wherein the diisocyanate in the step 2) is one or more of diphenylmethane diisocyanate, toluene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, 1, 5-naphthalene diisocyanate, p-phenylene diisocyanate, dimethylbiphenyl diisocyanate, and hexamethylene diisocyanate.
5. The method for preparing the moisture-permeable thermoplastic polyurethane film according to claim 1, wherein the small-molecule chain extender in the step 2) is one or more selected from ethylene glycol, 1, 2-propylene glycol, 1, 3-propylene glycol, 1, 4-butanediol, 1, 6-hexanediol, cyclohexanedimethanol, diethylene glycol, glycerol, ethylenediamine, triethanolamine, triisopropanolamine, diethyltoluenediamine, and N-methyldiethanolamine.
6. The method for preparing the moisture-permeable thermoplastic polyurethane film according to claim 1, wherein the blown width in the step 3) is 150cm to 160cm, the blown film thickness is 0.2mm to 0.5mm, and the temperature ranges of the three sections of the head of the film blowing unit are 155 ℃ to 175 ℃.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111285993A (en) * 2020-03-09 2020-06-16 江苏科技大学 Preparation method of high-fluidity polyamide 6 elastomer
CN117384476A (en) * 2023-11-23 2024-01-12 东莞市特普优环保新材料有限公司 TPU waterproof film and preparation method thereof

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