Water surface treatment agent for precoating metal material, furface treated metal material and precoating metallic material
A technology of surface treatment agent and metal material, which is applied in the direction of metal material coating process, device for coating liquid on the surface, anti-corrosion coating, etc., can solve the problem that the processing adhesion cannot be realized, the surface treatment agent is not practical, and cannot be realized The bending test is qualified, the processing adhesion and other problems are achieved, and the effects of good storage stability, cold bending adhesion and deep drawing performance, coin scratch resistance and moisture resistance are achieved.
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[0130] The following examples and comparative examples of the present invention are given to describe the present invention in detail, but the present invention is not limited to these examples.
[0131] 1. Preparation of water-based surface treatment agent
[0132] The silane coupling agent, polyurethane resin and polycarbodiimide compound described in Table 1 to Table 5, and the hexafluorometallic acid when used, other compounds that release fluoride ions when used, and the metal compound when used are according to the Sequentially add deionized water to reach the mass ratio of solid components shown in Table 1 to Table 5, and then stir for 5 minutes to fully disperse. Then, deionized water was added to adjust the solid content concentration to 7% by mass.
[0133] The components used are as follows.
[0134] Silane coupling agent (A) or equivalent
[0135] A1: γ-Aminopropyltrimethoxysilane
[0136] A2: 2-aminoethyl-3-aminopropyltrimethoxysilane
[0137] A3: γ-Glycidoxy...
manufacture example 1
[0180]Make 700 parts by mass (2.87mol) of m-tetramethylxylylene diisocyanate in 14 parts by mass of 3-methyl-1-phenyl-2-phosphene-1-oxide (carbodiimidization catalyst) The reaction was carried out at 180° C. for 32 hours in the presence of , to obtain a polycarbodiimide compound with isocyanate groups at both ends and a degree of condensation of 12. Add 115 parts by mass of polyoxyethylene monomethyl ether with a degree of polymerization of 12 to 224 parts by mass of the obtained polycarbodiimide compound, and react at 100°C for 48 hours to block the isocyanate groups at both ends, Then, 509 parts by mass of distilled water was slowly added at 50° C. to obtain an aqueous polycarbodiimide compound solution.
manufacture example 2
[0182] Make 338 mass parts (1.35mol) of diphenylmethane diisocyanate and 354 mass parts (1.35mol) of 4,4'-dicyclohexylmethane diisocyanate in 3-methyl-1-phenyl-2-cyclophosphene- The reaction was carried out at 180° C. for 32 hours in the presence of 2.9 parts by mass of 1-oxide to obtain a polycarbodiimide compound having isocyanate groups at both terminals and a degree of condensation of 12. Add 115 parts by mass of polyoxyethylene monomethyl ether with a degree of polymerization of 12 to 224 parts by mass of the obtained polycarbodiimide compound, and react at 100°C for 48 hours to block the isocyanate groups at both ends, and then 509 parts by mass of distilled water were slowly added at 50° C. to obtain an aqueous solution of a polycarbodiimide compound.
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