Unlock instant, AI-driven research and patent intelligence for your innovation.

Preparation method of polyurethane coating with flame retardancy, light resistance and low voc

A polyurethane coating and light resistance technology, applied in the preparation of light resistance and low VOC polyurethane coatings, flame retardant fields, can solve the problems of large toxic side effects, carcinogenicity, heavy metal tin hazards, etc., to improve the strength is not high, reduce VOC, increase The effect of absorbing small molecules

Active Publication Date: 2018-02-16
中山市海恒包装材料有限公司
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Dibutyltin dilaurate is often used as a catalyst for the polymerization of polyurethane, but since the heavy metal tin is harmful to the environment with the degradation of polyurethane, how to fix the residual tin catalyzed by dibutyltin dilaurate and reduce the impact of polyurethane coating residues on the environment The degree of harm has become a technical problem
[0004] In order to improve the light resistance of polyurethane resin, it is often used to add ultraviolet absorbers and antioxidants, but the traditional synthetic antioxidants include tert-butyl hydroxyanisole, tert-butyl hydroperoxide and tert-butyl hydroquinone, etc. Larger toxic and side effects and carcinogenicity, and the effect of improving water resistance with traditional silicone materials is not satisfactory, so it is necessary to find more efficient and environmentally friendly waterproof and light-resistant measures

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0038] (1) Preparation of modified manganese hypophosphite: Add 9g of manganese hypophosphite, 23g of boric acid, 20g of diethanolamine, 6.2g of hexaphenoxycyclotriphosphazene and 3- Aminopropyltrihydroxysilane 2.6g and water 60g, adjust the pH to 4, heat to 70°C, stir for 1h, add 2g of dipotassium EDTA, stir for 2h at 60°C to obtain modified manganese hypophosphite;

[0039] (2) Add 0.22g of triethylenetetramine, 70g of polytetrahydrofuran ether glycol and 15g of hexamethylene diisocyanate into a 250ml three-necked flask equipped with a stirrer, condenser and thermometer, and react at 80°C for 2h to obtain Polyurethane prepolymer A, the molecular weight of the polytetrahydrofuran ether glycol is 1000;

[0040] (3) Add 0.62g of acetamide and 8.2g of methyl ethyl ketone to prepolymer A, react at 75°C for 3.5h, add 2g of modified manganese hypophosphite prepared in step (1), 4g of 4-carboxyphenylboronic acid and di Ethylene triamine pentamethylene phosphonic acid 2.5g, reaction...

example 2

[0042] (1) Preparation of modified manganese hypophosphite: Add 6g of manganese hypophosphite, 10g of boric acid, 15g of diethanolamine, 12g of melamine cyanurate and 4-hydroxyphenylethylamine into a 250ml three-necked bottle with a stirrer and a thermometer 2.8g and 40g of water, adjust the pH to 4, heat to 70°C, stir for 1h, add 2g of dipotassium EDTA, stir for 1h at 60°C to obtain modified manganese hypophosphite;

[0043] (2) Add 0.64g of carbodiimide, 65g of polytetrahydrofuran ether glycol and 40g of hexamethylene diisocyanate into a 500ml three-necked flask equipped with a stirrer, condenser and thermometer, and react at 90°C for 2h to obtain Polyurethane prepolymer A, the molecular weight of the polytetrahydrofuran ether glycol is 2000;

[0044] (3) Add 3.2g of dithiothreitol and 16.5g of methyl ethyl ketone to prepolymer A, react at 75°C for 2.5h, add 6g of modified manganese hypophosphite prepared in step (1), 4-carboxybenzene Boric acid 3.4g and aminotrimethylene p...

example 3

[0046] (1) Preparation of modified manganese hypophosphite: Add 4.2g of manganese hypophosphite, 26g of boric acid, 22g of diethanolamine, 12g of hexamethylolmelamine and 4,8-dimethoxylate into a 250ml three-necked bottle with a stirrer and a thermometer. Hydroxyquinoline-2-carboxylic acid 2.2g and water 45g, adjust pH to 4, heat to 70°C, stir for 1h, dipotassium ethylenediaminetetraacetic acid 2g, 50°C for 1h, obtain modified manganese hypophosphite;

[0047] (2) Add 0.32g of sebacic acid dihydrazide, 85g of polytetrahydrofuran ether glycol and 32g of hexamethylene diisocyanate into a 500ml three-necked flask equipped with a stirrer, condenser and thermometer, and react at 75°C 1h, to obtain polyurethane prepolymer A, the molecular weight of the polytetrahydrofuran ether glycol is 1000;

[0048] (3) Add 2.4g of hexahydro-striazaborane and 20.4g of methyl ethyl ketone to prepolymer A, react at 70°C for 2.0h, add 8.9g of modified manganese hypophosphite prepared in step (1), 4 ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
wavelengthaaaaaaaaaa
Login to View More

Abstract

The invention discloses a preparation method of polyurethane paint with flame retardance, light resistance and low VOCs (volatile organic compounds). According to the method, 0.22g of triethylene tetramine, 70g of polytetrahydrofuran ether glycol and 15g of hexamethylene diisocyanate are added into a 250ml flask with three necks, wherein the flask with three necks is provided with a stirrer, a condensation tube and a thermometer; the reaction is performed for 2h at 80 DEG C to obtain a polyurethane prepolymer A; 0.62g of acetamide and 8.2g of ethyl methyl ketone are added into the prepolymer A; the reaction is performed for 3.5h under the condition of 75 DEG C; 2g of modified manganese hypophosphite prepared in the first step, 4g of 4-carboxyphenylboronic acid and 2.5g of diethylenetriaminepenta acid are added; the reaction temperature is 80 DEG C; the reaction time is 2h; 7.1g of triethylamine is added for neutralization reaction for 60min; 0.9g of vitamin C and 70g of water are added for stirring and emulsification; the polyurethane paint with flame retardance, light resistance and low VOCs is obtained. The prepared polyurethane paint with flame retardance, light resistance and low VOCs achieves an environment-friendly effect, has low cost, is widely applied to surfaces of walls, furniture and hardware, and is used as a bonding agent of plastics, glass, papermaking and spinning.

Description

technical field [0001] The invention relates to a method for preparing a polyurethane coating, in particular to a method for preparing a polyurethane coating with flame retardancy, light resistance and low VOC. Background technique [0002] Polyurethane is mainly used in leather finishing, textile printing and dyeing, paper making, architectural coatings and adhesives and other fields. Because the coatings and paints sprayed on the surface of internal and external walls, furniture or metal appliances are in direct or indirect contact with humans, toxic and harmful coatings are always threatening people's health. In addition, because the field of use is often exposed to sunlight, and the sun's rays contain a large amount of ultraviolet light harmful to colored objects, with a wavelength of about 290-460nm, these harmful ultraviolet rays cause the color of the paint to change through chemical oxidation and reduction. Variety. [0003] Dibutyltin dilaurate is often used as a ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C09D175/08C09D5/18C09D7/62C08G18/66C08G18/48C08G18/32C08G18/38C08G18/28C08G18/10
CPCC08G18/10C08G18/4854C08G18/6685C08K3/32C08K9/04C08K9/06C09D5/18C09D175/08C08G18/3876C08G18/3897C08G18/285
Inventor 邓海玻
Owner 中山市海恒包装材料有限公司