Primer-topcoat type solvent-free polyaspartic acid ester heavy anti-corrosion coating and preparation method and application thereof
A technology of aspartic acid ester and aspartic acid, which is applied in the direction of polyurea/polyurethane coatings, anti-corrosion coatings, coatings, etc., can solve the problems of increased construction costs, increased construction uncontrollability, high parking maintenance costs, etc., to achieve The curing rate is fast, the spraying ratio is stable, and the effect of improving construction efficiency
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[0032] In one embodiment according to the present invention, the preparation method of the modified filler comprises the following steps: (1) dissolving the silane coupling agent in absolute ethanol to prepare a solution with a mass concentration of 30-50%; (2) dissolving the The solution is sprayed on the filler in a high-speed mixer, stirred evenly at a high speed, dried in a blast drying oven at 100-105° C. for 2-5 hours, and then cooled naturally to obtain a modified filler.
[0033] In one embodiment according to the present invention, the silane coupling agent is γ-aminopropyltrimethoxysilane, N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, N-β - one or a combination of (aminoethyl)-γ-aminopropyltriethoxysilane and anilinomethyltrimethoxysilane.
[0034] In an embodiment according to the present invention, the preparation method of the hyperbranched modified aspartic acid resin comprises the following steps: (1) in a reaction kettle protected by an inert gas, add a mass ...
Embodiment 1
[0050] (1) prepare hyperbranched modified aspartic acid resin:
[0051] (1) In a nitrogen-protected reactor, add trichlorosilane ethanol solution with a mass concentration of 10-30%, add deionized water drop by drop under stirring, the molar ratio of deionized water to trichlorosilane is 1:3, React at a temperature of 75°C for 0.5 hours, then add hexamethylene diisocyanate, and continue to react for 0.5 hours to obtain a pre-reaction solution; Add hexamethylenediamine dropwise to the pre-reaction solution to end-cap, to obtain a silicon block branched modified organic diamine reaction solution; (3) in the above silicon block branched modified organic diamine reaction solution, use titration Dimethyl maleate was slowly added dropwise into the funnel. After the dropwise addition, the temperature was raised to 90°C for constant temperature reaction for 10 hours, then the solvent was removed and recovered, and the degree of reaction was determined by mercaptan-iodine titration ana...
Embodiment 2
[0058] (1) prepare hyperbranched modified aspartic acid resin:
[0059] (1) In the nitrogen-protected reactor, add trichlorosilane ethanol solution with a mass concentration of 30%, and add deionized water drop by drop under stirring. The molar ratio of deionized water to trichlorosilane is 1:3. React at 85°C for 1 hour, then add isophorone diisocyanate, and continue to react for 1 hour to obtain a pre-reaction liquid; Add 2,2,4-trimethyl-1,6-butanediamine dropwise to the pre-reaction liquid to end capping, and obtain a silicon block branched modified organic diamine reaction liquid; (3) in the above silicon block branched Diethyl maleate was slowly added dropwise into the chemically modified organic diamine reaction solution with a titration funnel. After the dropwise addition, the temperature was raised to 100°C for constant temperature reaction for 15 hours, and then the solvent was removed and recovered, and determined by mercaptan-iodine titration analysis method The deg...
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