CN114395359A - High-strength water-based polyurethane adhesive and preparation method thereof - Google Patents

High-strength water-based polyurethane adhesive and preparation method thereof Download PDF

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Publication number
CN114395359A
CN114395359A CN202111193531.3A CN202111193531A CN114395359A CN 114395359 A CN114395359 A CN 114395359A CN 202111193531 A CN202111193531 A CN 202111193531A CN 114395359 A CN114395359 A CN 114395359A
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parts
agent
polyurethane adhesive
resin
waterborne polyurethane
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朱佩
任亚明
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Nanjing Yige Polymer Composite New Material Technology Co ltd
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Nanjing Yige Polymer Composite New Material Technology Co ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • 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
    • C08G18/30Low-molecular-weight compounds
    • C08G18/34Carboxylic acids; Esters thereof with monohydroxyl compounds
    • C08G18/348Hydroxycarboxylic acids

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

The invention discloses a high-strength water-based polyurethane adhesive, which is characterized in that: the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 100-160 parts of waterborne polyurethane resin, 40-60 parts of hydrophilic chain extender, 40-60 parts of polyol, 20-45 parts of salt forming agent, 10-25 parts of thickener, 8-20 parts of flatting agent, 10-20 parts of defoamer, 8-16 parts of antioxidant, 15-25 parts of stannous octoate catalyst, 40-80 parts of acrylic resin and 6-15 parts of cross-linking agent; according to the invention, the acrylic resin is adopted in the formula, the acrylic resin and the waterborne polyurethane resin play a role in synergy, and the hydrophilic chain extender is adopted to avoid the defects of easy flocculation, poor stability, skinning and low solid content of the waterborne polyurethane adhesive to a certain extent.

Description

High-strength water-based polyurethane adhesive and preparation method thereof
Technical Field
The invention belongs to the technical field of waterborne polyurethane adhesives, and particularly relates to a high-strength waterborne polyurethane adhesive; in particular to a preparation method of the high-strength water-based polyurethane adhesive.
Background
The polyurethane adhesive has good comprehensive performance and performance adjustability, so the polyurethane adhesive is widely applied to bonding of buildings, automobiles, family decoration, packaging, printing, leather, artware and the like. Currently, polyurethane adhesives are classified into solvent-based, solvent-free, and aqueous polyurethane adhesives from the viewpoint of the use system. The solvent type polyurethane adhesive has the defects of environmental pollution and low solid content, and has great harm to operators in the gluing process. The solvent-free polyurethane adhesive is just developed in China, the synthesis process is complex, the performance obtained at present cannot be compared with that of a solvent-based polyurethane adhesive, the solvent-free polyurethane adhesive is mainly used for bonding a composite film, but has the advantage of environmental protection, and still needs to be developed vigorously.
However, the single aqueous polyurethane in the polyurethane adhesive has poor performance, mainly manifested by poor wettability to non-polar substrates, low adhesive strength and low initial adhesion, and cannot meet the requirements of various fields. In order to improve the performance of the waterborne polyurethane and expand the application field of the waterborne polyurethane, the waterborne polyurethane needs to be modified, so a high-strength waterborne polyurethane adhesive and a preparation method thereof are provided.
Disclosure of Invention
The invention aims to provide a high-strength water-based polyurethane adhesive and a preparation method thereof, and aims to solve the problems of poor wettability, low bonding strength and low initial adhesion to a non-polar substrate and incapability of meeting the requirements of various fields in the background art.
In order to achieve the purpose, the invention adopts the following technical scheme:
the high-strength aqueous polyurethane adhesive comprises the following components in parts by weight: 100-160 parts of waterborne polyurethane resin, 40-60 parts of hydrophilic chain extender, 40-60 parts of polyol, 20-45 parts of salt forming agent, 10-25 parts of thickener, 8-20 parts of flatting agent, 10-20 parts of defoamer, 8-16 parts of antioxidant, 15-25 parts of stannous octoate catalyst, 40-80 parts of acrylic resin and 6-15 parts of cross-linking agent;
the waterborne polyurethane resin is prepared from micromolecular polybasic acid and micromolecular polyalcohol, wherein the micromolecular polybasic acid and the micromolecular polyalcohol are prepared according to the molar ratio of alkyd acid to alkyd acid of 1: 1-1.4: 1, adding the mixture into a reaction container, adding a stannous octoate catalyst, gradually heating to 220-230 ℃ under the protection of nitrogen, and carrying out heat preservation reaction for 90-120 minutes; then decompressing to-0.095 to-0.1 MPa at the temperature of 220-230 ℃, and stopping the reaction after the acid value is reduced to below 1.0, thus obtaining the waterborne polyurethane resin.
As a preferred technical scheme, the thickening agent is one or a mixture of more of terpene resin, phenolic resin, acrylic copolymer and rosin resin; the salt forming agent is triethylamine; the defoaming agent is a polyoxy enol amine ether defoaming agent; the leveling agent is a modified organic silicon leveling agent.
As a preferable technical solution, the hydrophilic chain extender is one or a combination of two of dimethylolpropionic acid and dimethylolbutyric acid.
As a preferred technical scheme, the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 100 parts of waterborne polyurethane resin, 40 parts of hydrophilic chain extender, 40 parts of polyol, 20 parts of salt forming agent, 10 parts of thickening agent, 8 parts of flatting agent, 10 parts of defoaming agent, 8 parts of antioxidant, 15 parts of stannous octoate catalyst, 40 parts of acrylic resin and 6 parts of crosslinking agent.
As a preferred technical scheme, the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 160 parts of waterborne polyurethane resin, 60 parts of hydrophilic chain extender, 60 parts of polyol, 45 parts of salt forming agent, 25 parts of thickening agent, 20 parts of flatting agent, 20 parts of defoaming agent, 16 parts of antioxidant, 25 parts of stannous octoate catalyst, 80 parts of acrylic resin and 15 parts of crosslinking agent.
As a preferred technical scheme, the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 130 parts of waterborne polyurethane resin, 50 parts of hydrophilic chain extender, 50 parts of polyol, 33 parts of salt forming agent, 18 parts of thickening agent, 16 parts of flatting agent, 15 parts of defoaming agent, 12 parts of antioxidant, 20 parts of stannous octoate catalyst, 65 parts of acrylic resin and 10 parts of crosslinking agent.
A preparation method of a high-strength water-based polyurethane adhesive comprises the following steps:
s1, preparing the waterborne polyurethane resin, namely preparing the waterborne polyurethane resin by adopting micromolecular polybasic acid and micromolecular polyalcohol;
s2, preparing materials, namely weighing all the materials according to the formula of the high-strength water-based polyurethane adhesive and strictly according to the mass parts for later use;
s3, treating the aqueous polyurethane resin, selecting the aqueous polyurethane resin, heating to 108-110 ℃, vacuumizing to-0.90-0.1 MPa, dehydrating in vacuum for 120-180 minutes, and cooling to 50-60 ℃;
s4, preparing a prepolymer, adding acrylic resin according to the dosage relation, reacting for 90-120 minutes at 50-55 ℃, heating to 70-100 ℃, and continuing to react for 100-150 minutes to obtain the prepolymer;
s5, reducing the temperature of the prepolymer to below 50 ℃, adding a hydrophilic chain extender according to the dosage relation, and then heating to 70-80 ℃ for heat preservation reaction for 2-4 hours;
s7, after the heat preservation time is reached, reducing the temperature of the prepolymer to below 50 ℃, adding a salt forming agent and a crosslinking agent, raising the temperature to 70-80 ℃ again, and carrying out heat preservation reaction for 1-2 hours;
and S8, sequentially adding the thickening agent, the defoaming agent, the flatting agent and the antioxidant into the prepolymer according to the dosage relationship, stirring at the temperature of 40-50 ℃, cooling to normal temperature and standing for 30 minutes.
As a preferable technical scheme, the stirring speed in the step S8 is 600-1200r/min, and the stirring time is 90-120 min.
The invention has the technical effects and advantages that:
according to the invention, the acrylic resin is adopted in the formula, the acrylic resin and the waterborne polyurethane resin play a role in synergy, and the hydrophilic chain extender is adopted to avoid the defects of easy flocculation, poor stability, skinning and low solid content of the waterborne polyurethane adhesive to a certain extent.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present invention more apparent, the technical solutions of the embodiments of the present invention will be clearly and completely described below, and it is apparent that the described embodiments are some embodiments of the present invention, but not all embodiments. All other embodiments, which can be obtained by a person skilled in the art without any inventive step based on the embodiments of the present invention, are within the scope of the present invention. Thus, the following detailed description of embodiments of the invention is not intended to limit the scope of the invention as claimed, but is merely representative of selected embodiments of the invention. All other embodiments, which can be obtained by a person skilled in the art without any inventive step based on the embodiments of the present invention, are within the scope of the present invention.
Example 1
The high-strength aqueous polyurethane adhesive comprises the following components in parts by weight: 100 parts of waterborne polyurethane resin, 40 parts of hydrophilic chain extender, 40 parts of polyol, 20 parts of salt forming agent, 10 parts of thickening agent, 8 parts of flatting agent, 10 parts of defoaming agent, 8 parts of antioxidant, 15 parts of stannous octoate catalyst, 40 parts of acrylic resin and 6 parts of crosslinking agent;
the waterborne polyurethane resin is prepared from micromolecular polybasic acid and micromolecular polyalcohol, wherein the micromolecular polybasic acid and the micromolecular polyalcohol are prepared according to the molar ratio of alkyd acid to alkyd acid of 1: 1-1.4: 1, adding the mixture into a reaction container, adding a stannous octoate catalyst, gradually heating to 220-230 ℃ under the protection of nitrogen, and carrying out heat preservation reaction for 90-120 minutes; then decompressing to-0.095 to-0.1 MPa at the temperature of 220-230 ℃, and stopping the reaction after the acid value is reduced to below 1.0 to obtain the waterborne polyurethane resin;
the thickening agent is one or a mixture of more of terpene resin, phenolic resin, acrylic copolymer and rosin resin; the salt forming agent is triethylamine; the defoaming agent is polyoxyethylene alcohol amine ether defoaming agent; the flatting agent is a modified organic silicon flatting agent; the hydrophilic chain extender is one or the combination of two of dimethylolpropionic acid and dimethylolbutyric acid;
a preparation method of a high-strength water-based polyurethane adhesive comprises the following steps:
s1, preparing the waterborne polyurethane resin, namely preparing the waterborne polyurethane resin by adopting micromolecular polybasic acid and micromolecular polyalcohol;
s2, preparing materials, namely weighing all the materials according to the formula of the high-strength water-based polyurethane adhesive and strictly according to the mass parts for later use;
s3, treating the aqueous polyurethane resin, selecting the aqueous polyurethane resin, heating to 108-110 ℃, vacuumizing to-0.90-0.1 MPa, dehydrating in vacuum for 120-180 minutes, and cooling to 50-60 ℃;
s4, preparing a prepolymer, adding acrylic resin according to the dosage relation, reacting for 90-120 minutes at 50-55 ℃, heating to 70-100 ℃, and continuing to react for 100-150 minutes to obtain the prepolymer;
s5, reducing the temperature of the prepolymer to below 50 ℃, adding a hydrophilic chain extender according to the dosage relation, and then heating to 70-80 ℃ for heat preservation reaction for 2-4 hours;
s7, after the heat preservation time is reached, reducing the temperature of the prepolymer to below 50 ℃, adding a salt forming agent and a crosslinking agent, raising the temperature to 70-80 ℃ again, and carrying out heat preservation reaction for 1-2 hours;
s8, sequentially adding a thickening agent, a defoaming agent, a flatting agent and an antioxidant into the prepolymer according to the dosage relationship, stirring at the temperature of 40-50 ℃, cooling to normal temperature and standing for 30 minutes;
wherein the stirring speed in the step S8 is 600-1200r/min, and the stirring time is 90-120 min.
Example 2
The difference in example 1 is that:
optionally, the formula of the high-strength aqueous polyurethane adhesive comprises the following components in parts by weight: 160 parts of waterborne polyurethane resin, 60 parts of hydrophilic chain extender, 60 parts of polyol, 45 parts of salt forming agent, 25 parts of thickening agent, 20 parts of flatting agent, 20 parts of defoaming agent, 16 parts of antioxidant, 25 parts of stannous octoate catalyst, 80 parts of acrylic resin and 15 parts of crosslinking agent;
the waterborne polyurethane resin is prepared from micromolecular polybasic acid and micromolecular polyalcohol, wherein the micromolecular polybasic acid and the micromolecular polyalcohol are prepared according to the molar ratio of alkyd acid to alkyd acid of 1: 1-1.4: 1, adding the mixture into a reaction container, adding a stannous octoate catalyst, gradually heating to 220-230 ℃ under the protection of nitrogen, and carrying out heat preservation reaction for 90-120 minutes; then decompressing to-0.095 to-0.1 MPa at the temperature of 220-230 ℃, and stopping the reaction after the acid value is reduced to below 1.0 to obtain the waterborne polyurethane resin;
the thickening agent is one or a mixture of more of terpene resin, phenolic resin, acrylic copolymer and rosin resin; the salt forming agent is triethylamine; the defoaming agent is polyoxyethylene alcohol amine ether defoaming agent; the flatting agent is a modified organic silicon flatting agent; the hydrophilic chain extender is set to be one or the combination of two of dimethylolpropionic acid and dimethylolbutyric acid.
Example 3
The differences from example 1 and example 2 are:
optionally, the formula of the high-strength aqueous polyurethane adhesive comprises the following components in parts by weight: 130 parts of waterborne polyurethane resin, 50 parts of hydrophilic chain extender, 50 parts of polyol, 33 parts of salt forming agent, 18 parts of thickening agent, 16 parts of flatting agent, 15 parts of defoaming agent, 12 parts of antioxidant, 20 parts of stannous octoate catalyst, 65 parts of acrylic resin and 10 parts of crosslinking agent;
the waterborne polyurethane resin is prepared from micromolecular polybasic acid and micromolecular polyalcohol, wherein the micromolecular polybasic acid and the micromolecular polyalcohol are prepared according to the molar ratio of alkyd acid to alkyd acid of 1: 1-1.4: 1, adding the mixture into a reaction container, adding a stannous octoate catalyst, gradually heating to 220-230 ℃ under the protection of nitrogen, and carrying out heat preservation reaction for 90-120 minutes; then decompressing to-0.095 to-0.1 MPa at the temperature of 220-230 ℃, and stopping the reaction after the acid value is reduced to below 1.0 to obtain the waterborne polyurethane resin;
the thickening agent is one or a mixture of more of terpene resin, phenolic resin, acrylic copolymer and rosin resin; the salt forming agent is triethylamine; the defoaming agent is polyoxyethylene alcohol amine ether defoaming agent; the flatting agent is a modified organic silicon flatting agent; the hydrophilic chain extender is set to be one or the combination of two of dimethylolpropionic acid and dimethylolbutyric acid.
The specific formulation data for three sets of examples of the invention are given in the following table:
example 1 Example 2 Example 3
Aqueous polyurethane resin 100 portions of 160 portions of 130 portions of
Hydrophilic chain extender 40 portions of 60 portions of 50 portions of
Polyhydric alcohols 40 portions of 60 portions of 50 portions of
Salt forming agent 20 portions of 45 portions of 33 portions of
Thickening agent 10 portions of 25 portions of 18 portions of
Leveling agent 8 portions of 20 portions of 16 portions of
Defoaming agent 10 portions of 20 portions of 15 portions of
Antioxidant agent 8 portions of 16 portions of 12 portions of
Stannous octoate catalyst 15 portions of 25 portions of 20 portions of
Acrylic resin 40 portions of 80 portions 65 portions of
Crosslinking agent 6 portions of 15 portions of 10 portions of
According to the invention, the acrylic resin is adopted in the formula, the acrylic resin and the waterborne polyurethane resin play a role in synergy, and the hydrophilic chain extender is adopted to avoid the defects of easy flocculation, poor stability, skinning and low solid content of the waterborne polyurethane adhesive to a certain extent.
The above description is only for the preferred embodiment of the present invention, but the scope of the present invention is not limited thereto, and any person skilled in the art should be considered to be within the technical scope of the present invention, and the technical solutions and the inventive concepts thereof according to the present invention should be equivalent or changed within the scope of the present invention.
It should be noted that, in this document, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus.

Claims (8)

1. A high-strength water-based polyurethane adhesive is characterized in that: the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 100-160 parts of waterborne polyurethane resin, 40-60 parts of hydrophilic chain extender, 40-60 parts of polyol, 20-45 parts of salt forming agent, 10-25 parts of thickener, 8-20 parts of flatting agent, 10-20 parts of defoamer, 8-16 parts of antioxidant, 15-25 parts of stannous octoate catalyst, 40-80 parts of acrylic resin and 6-15 parts of cross-linking agent;
the waterborne polyurethane resin is prepared from micromolecular polybasic acid and micromolecular polyalcohol, wherein the micromolecular polybasic acid and the micromolecular polyalcohol are prepared according to the molar ratio of alkyd acid to alkyd acid of 1: 1-1.4: 1, adding the mixture into a reaction container, adding a stannous octoate catalyst, gradually heating to 220-230 ℃ under the protection of nitrogen, and carrying out heat preservation reaction for 90-120 minutes; then decompressing to-0.095 to-0.1 MPa at the temperature of 220-230 ℃, and stopping the reaction after the acid value is reduced to below 1.0, thus obtaining the waterborne polyurethane resin.
2. The high-strength aqueous polyurethane adhesive according to claim 1, wherein: the thickening agent is one or a mixture of more of terpene resin, phenolic resin, acrylic copolymer and rosin resin; the salt forming agent is triethylamine; the defoaming agent is a polyoxy enol amine ether defoaming agent; the leveling agent is a modified organic silicon leveling agent.
3. The high-strength aqueous polyurethane adhesive according to claim 1, wherein: the hydrophilic chain extender is one or two of dimethylolpropionic acid and dimethylolbutyric acid.
4. The high-strength aqueous polyurethane adhesive according to claim 1, wherein: the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 100 parts of waterborne polyurethane resin, 40 parts of hydrophilic chain extender, 40 parts of polyol, 20 parts of salt forming agent, 10 parts of thickening agent, 8 parts of flatting agent, 10 parts of defoaming agent, 8 parts of antioxidant, 15 parts of stannous octoate catalyst, 40 parts of acrylic resin and 6 parts of crosslinking agent.
5. The high-strength aqueous polyurethane adhesive according to claim 1, wherein: the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 160 parts of waterborne polyurethane resin, 60 parts of hydrophilic chain extender, 60 parts of polyol, 45 parts of salt forming agent, 25 parts of thickening agent, 20 parts of flatting agent, 20 parts of defoaming agent, 16 parts of antioxidant, 25 parts of stannous octoate catalyst, 80 parts of acrylic resin and 15 parts of crosslinking agent.
6. The high-strength aqueous polyurethane adhesive according to claim 1, wherein: the formula of the high-strength water-based polyurethane adhesive comprises the following components in parts by weight: 130 parts of waterborne polyurethane resin, 50 parts of hydrophilic chain extender, 50 parts of polyol, 33 parts of salt forming agent, 18 parts of thickening agent, 16 parts of flatting agent, 15 parts of defoaming agent, 12 parts of antioxidant, 20 parts of stannous octoate catalyst, 65 parts of acrylic resin and 10 parts of crosslinking agent.
7. The preparation method of the high-strength aqueous polyurethane adhesive as claimed in claim 1, which comprises the following steps:
s1, preparing the waterborne polyurethane resin, namely preparing the waterborne polyurethane resin by adopting micromolecular polybasic acid and micromolecular polyalcohol;
s2, preparing materials, namely weighing all the materials according to the formula of the high-strength water-based polyurethane adhesive and strictly according to the mass parts for later use;
s3, treating the aqueous polyurethane resin, selecting the aqueous polyurethane resin, heating to 108-110 ℃, vacuumizing to-0.90-0.1 MPa, dehydrating in vacuum for 120-180 minutes, and cooling to 50-60 ℃;
s4, preparing a prepolymer, adding acrylic resin according to the dosage relation, reacting for 90-120 minutes at 50-55 ℃, heating to 70-100 ℃, and continuing to react for 100-150 minutes to obtain the prepolymer;
s5, reducing the temperature of the prepolymer to below 50 ℃, adding a hydrophilic chain extender according to the dosage relation, and then heating to 70-80 ℃ for heat preservation reaction for 2-4 hours;
s7, after the heat preservation time is reached, reducing the temperature of the prepolymer to below 50 ℃, adding a salt forming agent and a crosslinking agent, raising the temperature to 70-80 ℃ again, and carrying out heat preservation reaction for 1-2 hours;
and S8, sequentially adding the thickening agent, the defoaming agent, the flatting agent and the antioxidant into the prepolymer according to the dosage relationship, stirring at the temperature of 40-50 ℃, cooling to normal temperature and standing for 30 minutes.
8. The method for preparing the high-strength aqueous polyurethane adhesive according to claim 7, wherein: the stirring speed in the step S8 is 600-1200r/min, and the stirring time is 90-120 min.
CN202111193531.3A 2021-10-13 2021-10-13 High-strength water-based polyurethane adhesive and preparation method thereof Pending CN114395359A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115044338A (en) * 2022-07-22 2022-09-13 合肥科天水性科技有限责任公司 Water-based formaldehyde-free adhesive for cigarette packaging and preparation method and application thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101182406A (en) * 2007-12-14 2008-05-21 华南理工大学 Method for preparing multiple modified self-crosslinking aqueous polyurethane adhesive agent
CN101348703A (en) * 2008-06-20 2009-01-21 中山大学 Aqueous polyurethane adhesive and preparation thereof
CN102936480A (en) * 2012-11-08 2013-02-20 无锡市万力粘合材料有限公司 Waterborne polyurethane adhesive for fabric and preparation method thereof
CN105820792A (en) * 2016-05-11 2016-08-03 南京京锦元科技实业有限公司 Waterborne polyurethane adhesive with high water resistance and strength and application thereof
CN109135656A (en) * 2018-07-26 2019-01-04 广东康和新材有限公司 A kind of water-based polyurethane adhesive and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101182406A (en) * 2007-12-14 2008-05-21 华南理工大学 Method for preparing multiple modified self-crosslinking aqueous polyurethane adhesive agent
CN101348703A (en) * 2008-06-20 2009-01-21 中山大学 Aqueous polyurethane adhesive and preparation thereof
CN102936480A (en) * 2012-11-08 2013-02-20 无锡市万力粘合材料有限公司 Waterborne polyurethane adhesive for fabric and preparation method thereof
CN105820792A (en) * 2016-05-11 2016-08-03 南京京锦元科技实业有限公司 Waterborne polyurethane adhesive with high water resistance and strength and application thereof
CN109135656A (en) * 2018-07-26 2019-01-04 广东康和新材有限公司 A kind of water-based polyurethane adhesive and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115044338A (en) * 2022-07-22 2022-09-13 合肥科天水性科技有限责任公司 Water-based formaldehyde-free adhesive for cigarette packaging and preparation method and application thereof

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Application publication date: 20220426