Preparation method of high-solid-content star acrylate polyurethane dispersion for coating varnish
A technology of acrylic polyurethane and varnish, which is applied in the direction of coating, etc., and can solve problems such as environmental pollution
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Embodiment 1
[0031] (1) Heat 20g of hexamethylene isocyanate trimer and 1g of trimethylolpropane in a reaction kettle to 50-60°C, and react until the NCO content is 13.3% to obtain 21g of A1;
[0032] (2) React 21g A1 and 24g hydroxyethyl acrylate to NCO content at 60-80℃ <0.1%, 45gA2 is obtained;
[0033] (3) Add 45 g of propylene glycol methyl ether to 45 g of A2 to obtain 90 g of A3;
[0034] (4) Heat 90g A3 to 120-140℃, then mix the uniformly mixed acrylic acid 10g, n-butyl acrylate 50g, isobornyl acrylate 10g, methyl methacrylate 15g and initiator dicumyl peroxide 3g , Add dropwise to A3 at a constant speed within 3h, keep for 1h after dripping, to obtain 178g A4;
[0035] (5) Cool 178g A4 to 100°C, and extract 33g propylene glycol methyl ether under a negative pressure of 0.08MPa to obtain 145g A5;
[0036] (6) Cool 145g A5 to 60°C, add 12g neutralizer dimethylethanolamine dropwise at a constant speed within 0.5h, keep the temperature and stir for 15min to obtain 167g A6;
[0037] (7) Add 54 g...
Embodiment 2
[0039] (1) Heat 25 g of hexamethylene isocyanate trimer and 1.1 g of trimethylolpropane in a reaction kettle to 50-60° C., and react until the NCO content is 16.5% to obtain 26.1 g of A1;
[0040] (2) React 21g A1 with 28g hydroxyethyl acrylate to NCO content at 60-80℃ <0.1% to obtain 54.1gA2;
[0041] (3) Add 45 g of propylene glycol butyl ether to 54.1 g of A2 to obtain 99.1 g of A3;
[0042] (4) Heat 99.1g A3 to 120-140℃, and then mix the uniformly mixed 10g acrylic acid, 40g n-butyl acrylate, 10g isobornyl acrylate, 20g methyl methacrylate and initiator tert-butyl peroxide 2.4g, added dropwise to A3 at a constant rate within 3h, keep it for 1h after dripping, to obtain 181.5g A4;
[0043] (5) Cool 181.5g A4 to 100°C, and extract 32.5g propylene glycol butyl ether under a negative pressure of 0.08MPa to obtain 149g A5;
[0044] (6) Cool 149g of A5 to 60°C, add 12g of neutralizing agent dimethylethanolamine dropwise at a constant speed within 0.5h, keep the temperature and stir for 1...
Embodiment 3
[0047] (1) Heat 25 g of hexamethylene isocyanate trimer and 1.1 g of trimethylolpropane in a reaction kettle to 50-60° C., and react until the NCO content is 16.5% to obtain 26.1 g of A1;
[0048] (2) 21g A1 and 30g hydroxypropyl acrylate are reacted to NCO content at 60-80℃ <0.1% to obtain 56.1gA2;
[0049] (3) Add 45 g of propylene glycol butyl ether to 56.1 g of A2 to obtain 101.1 g of A3;
[0050] (4) Heat 101.1g A3 to 120-140℃, and then mix uniformly 9g acrylic acid, 40g n-butyl acrylate, 9g isobornyl acrylate, 20g methyl methacrylate and initiator tert-butyl peroxide. 2.4g, added dropwise to A3 at a constant rate within 3h, keep it for 1h after dripping, to obtain 181.5g A4;
[0051] (5) Cool 181.5g A4 to 100°C, and extract 32.5g propylene glycol butyl ether under a negative pressure of 0.08MPa to obtain 149g A5;
[0052] (6) Cool 149g of A5 to 60°C, add 12g of neutralizing agent dimethylethanolamine dropwise at a constant speed within 0.5h, keep the temperature and stir for 15mi...
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