Solvent-free composite binding agent for solar back board and preparation method thereof
A technology for solar back sheets and adhesives, applied in the directions of adhesive additives, polymer adhesive additives, non-polymer adhesive additives, etc., can solve the problem of high requirements for multi-layer co-extrusion composite film equipment and limited resin types , the problem of high equipment price, to achieve the effect of increasing the initial peel strength, low viscosity and low initial viscosity
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[0024] A kind of preparation method of solvent-free composite adhesive for solar back sheet of the present invention, it comprises the following steps:
[0025] (a) Preparation of component A: Put the small molecule diol into the reaction kettle, add polyether polyol, catalyst, leveling agent, adhesion promoter, and antioxidant in turn, and stir at 25°C for 1 hour to prepare Get A component;
[0026] (b) Preparation of polyether whose end group is -NCO in component B: put the polyether polyol in a three-necked flask, and under the protection of nitrogen atmosphere, heat up to 60-70°C, and add polyisocyanate (-OH / -NCO=1:1), take samples after reacting for 4 to 5 hours, measure the content of -NCO group, stop the reaction when the mass percentage of -NCO changes ≤ 0.02%, and the number average molecular weight of polyether polyol is between 600 and 3000 Polyoxypropylene diol or triol, polyoxypropylene and oxyethylene copolymer diol or triol, polytetrahydrofuran diol or triol, ...
Embodiment 1
[0036] Preparation of component A: put 20g of ethylene glycol into the reaction kettle, add 100g of polyoxypropylene glycol, 5g of triethylenetetramine, 10g of polydimethylsiloxane, bis-[γ-(triethoxy Silicon) propyl] tetrasulfide (Si-69) 5g, 2,6-di-tert-butyl-4-methylphenol 0.1g, stirred at 25°C for 1h to prepare component A.
[0037] Preparation of polyether whose end group is -NCO in component B: put 100g of polyoxypropylene diol in a three-necked flask, under the protection of nitrogen atmosphere, heat up to 60°C, add 100g of toluene diisocyanate (to -OH / -NCO=1:1), take a sample after 4 hours of reaction, measure the content of -NCO group, and stop the reaction when the mass percentage of -NCO changes ≤ 0.02%.
[0038] Preparation of component B: Put 90 parts of the above-mentioned polyether whose end group is -NCO into the reaction kettle, add 1 g of benzoyl chloride and 0.1 g of polycarbodiimide in sequence, and stir at 25°C for 1 hour to prepare component B .
[0039]...
Embodiment 2
[0042] Preparation of component A: put 25g of 1,4-butanediol into the reaction kettle, add 100g of polyoxypropylene and ethylene oxide copolymer diol, 6g of methyldiethanolamine, 10g of polyether modified silicone, bis -[γ-(triethoxysilyl)propyl]disulfide (Si-75) 6g, 2,2'-methylene bis(4-methyl-6-tert-butylphenol) 0.2g, 25 Stir at ℃ for 1 h to obtain component A.
[0043] Preparation of polyether whose end group is -NCO in component B: put 100g of polyoxypropylene and ethylene oxide copolymer triol in a three-necked flask, under the protection of nitrogen atmosphere, heat up to 65°C, and add 90g of diphenyl Methyl methane diisocyanate (to -OH / -NCO = 1:1), take a sample after 4.5 hours of reaction, measure the content of -NCO group, and stop the reaction when the mass percentage of -NCO changes ≤ 0.02%.
[0044] Preparation of component B: Put 90 parts of the above-mentioned polyether whose end group is -NCO into a reaction kettle, add 2 g of phosphoric acid and 0.3 g of polyc...
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