Process for preparing ultraviolet curable aqueous polyurethane resin

A water-based polyurethane and ultraviolet light technology, which is applied in the field of polyurethane coatings and adhesives, can solve the problems that the resistance to methyl ethyl ketone wiping performance cannot be improved, the performance of methyl ethyl ketone wiping resistance is not improved, and the hardness of the coating is not high. Good wiping performance and high coating hardness

Inactive Publication Date: 2006-10-11
UNIV OF SCI & TECH OF CHINA +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

Chinese Patent Application No. 200410063171.5 proposes a method for the preparation of UV-curable water-based polyurethane resin, which uses soft segment unsaturated polyester acrylate containing double bonds to introduce double bonds into polyurethane molecular chains, because this method is increasing the content of double bonds When the hard segment content will be reduced accordingly, the hardness of the obtained coating will not increase, and it is only suitable for soft touch coatings; its resis

Method used

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  • Process for preparing ultraviolet curable aqueous polyurethane resin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Add 36.7 grams of PTMG into a 500ml three-necked flask, dehydrate at 100°C for 1.5 hours, add 47.9 grams of IPDI, stir and react at 100°C for 2 hours, add 6.5 grams of hydrophilic chain extender DA, and stir at 90°C for 2 After one hour, add 22 grams of acetone, 45 grams of pentaerythritol tetraacrylate, 2.8 grams of p-methoxyphenol and 0.073 grams of dibutyltin dilaurate, and stir and react at 80°C for 2 hours, then add 6 grams of HEA, After stirring and reacting at 70°C for 2 hours, transfer the polyurethane resin into a high-speed shear disperser, add 5 grams of triethylamine at 800 rpm and 40°C, and react for 1 minute, then add 272 grams of water, and after 5 minutes , to obtain a UV-curable water-based polyurethane resin emulsion; transfer it to a rotary evaporator, remove acetone at 40°C and -0.1MPa vacuum conditions, and obtain a UV-curable water-based polyurethane resin.

[0021] The structure of the polyurethane resin can be characterized by infrared spectrum. ...

Embodiment 2

[0024] Add 35.8 grams of PJ into a 500ml three-neck flask, dehydrate at 110°C for 1 hour, add 75.5 grams of MDI, stir and react at 80°C for 4 hours, add 12.3 grams of hydrophilic chain extender DA, and stir at 60°C for 4 After 1 hour, add 55 grams of methyl ethyl ketone, 36.6 grams of PEDA, 0.09 grams of hydroquinone and 0.018 grams of dibutyltin dilaurate, stir and react at 50 ° C for 4 hours, add 12 grams of HPA, and stir and react at 50 ° C for 3 hours , put it into a high-speed shear disperser, add 9.5 grams of triethylamine at 2000 rpm and 30 ° C, react for 2 minutes, add 418 grams of water, and after 1 minute, the UV-curable water-based Polyurethane resin emulsion; transfer to a rotary evaporator, remove acetone at 50°C and 0.09MPa vacuum to obtain a UV-curable waterborne polyurethane resin.

[0025] The structural characterization of the polyurethane resin is the same as in Example 1.

Embodiment 3

[0027] Add 95 kg of PCD and HTTP mixture into a 50L reactor, dehydrate at 120°C for 0.5 hours, add 64.8 kg of TDI, react at 90°C for 3 hours, add 8 kg of hydrophilic chain extender DA, in After reacting at 80°C for 1 hour, add 58.5 kg of acetone, 31.1 kg of TMPME, 3 kg of BHT and 0.069 kg of dibutyltin dilaurate, stir and react at 65°C for 3 hours, add 22.4 kg of PETA, and stir at 60°C for 2.5 hours , into a high-speed shear disperser, add 6.5 kg of triethylamine at 4000 rpm and 20°C, react for 3 minutes, add 342 kg of water, and after 3 minutes, you can get a UV-curable water-based polyurethane resin emulsion .

[0028] Transfer it to a solvent removal kettle, and remove acetone under 60°C and 0.08MPa vacuum conditions to obtain a UV-curable water-based polyurethane resin. The structural characterization of the polyurethane resin is the same as in Example 1.

[0029] If other conditions of this embodiment remain unchanged, and PCD or HTTP is replaced by PJ or PTMG, or any c...

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Abstract

This invention is the preparation method of ultraviolet light stabilized polyurethane resin with aquosity. The procedure is as followings: add diatomic alcohol with isoallyl group, solvent, polymerization inhibitor and catalysis into polyurethane. React at 50-80deg C for 2-4hours. Add hydroxyethyl methacrylate to react at 50-70deg C for 2-3hours. Use diatomic alcohol with isoallyl group to amplify the NCO group and polyurethane pre-polymer. Then cap with hydroxyethyl methacrylate to add acroleic acid double bond into polyurethane's branch chain and chain ends. With this method, polyurethane is NCOgroup-free. It helps increase the emulsion's storage stability. This invention increase the product's double bonds contents as well as hard block contents to lift crosslinking density, coating hardness and resistance of wiping with methyl-ethyl ketone.

Description

Technical field: [0001] The invention belongs to the technical field of polyurethane coatings and adhesives, in particular to a preparation method of an ultraviolet (UV) curable waterborne polyurethane resin used for a hard coating. Background technique: [0002] UV-curable waterborne polyurethane resin is widely used in the field of coatings because of its good comprehensive performance and outstanding environmental protection. Chinese Patent Application No. 200410063171.5 proposes a method for the preparation of UV-curable water-based polyurethane resin, which uses soft segment unsaturated polyester acrylate containing double bonds to introduce double bonds into polyurethane molecular chains, because this method is increasing the content of double bonds When the hard segment content will be reduced accordingly, the hardness of the obtained coating will not increase, and it is only suitable for soft touch coatings; its resistance to methyl ethyl ketone wiping performance ha...

Claims

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Application Information

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IPC IPC(8): C08G18/10C08G18/40C08G18/76C08G18/83C08K5/13
Inventor 戴家兵张兴元白晨艳于子洲
Owner UNIV OF SCI & TECH OF CHINA
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