Nano self-assembly penetrant for magnesium alloy service and preparation method and application thereof
A nano-self-assembly and penetrating agent technology, applied in anodic oxidation, phosphating, etc., can solve problems such as effective protection of difficult magnesium alloy substrates, peeling off of composite coatings, corrosion, etc., to improve overall protection performance and bonding performance, and prolong service life Lifespan, the effect of accelerating the hydrolysis reaction
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Embodiment 1
[0031] 1. Configuration of silane mixture. Mix and stir the silane KH-560 and TEOS at a molar ratio of n(KH560):n(TEOS)=3:1 to obtain a silane mixture.
[0032] 2. Configuration of hydrolysis catalyst. Acetic acid and phytic acid are uniformly mixed in a molar ratio of n (acetic acid):n (phytic acid) to 2:1 to obtain a hydrolysis catalyst.
[0033] 3. Co-solvent configuration. The co-solvent is propanol.
[0034] 4. Configuration of hydrolysis reaction. At room temperature, mix the silane mixed solution, hydrolysis catalyst, co-solvent and deionized water according to the following parts by weight, continue to stir, and hydrolyze for 3 to 4 days until the mixed solution is clear, then age it for later use to obtain liquid A.
[0035]
[0036] 5. Configuration of curing agent. The curing agent is triethylenetetramine (TETA), and TETA is made into a 10mol / L aqueous solution to obtain liquid B.
[0037] 6. Configuration of cross-linking reaction. At room temperature, ad...
Embodiment 2
[0042] 1. Configuration of silane mixture. Silane KH-560, Si69 and TEOS were mixed and stirred at a molar ratio of n(KH560):n(Si69):n(TEOS)=1.5:1.1:1 to obtain a silane mixture.
[0043] 2. Configuration of hydrolysis catalyst. Acetic acid and phytic acid are uniformly mixed in a molar ratio of n(acetic acid):n(phytic acid)=1.5:0.4 to obtain a hydrolysis catalyst.
[0044] 3. Co-solvent configuration. Co-solvent is selected ethanol.
[0045] 4. Configuration of hydrolysis reaction. At room temperature, mix the silane mixed solution, hydrolysis catalyst, co-solvent and deionized water according to the following parts by weight, continue to stir, and hydrolyze for 3 to 4 days until the mixed solution is clear, then age it for later use to obtain liquid A.
[0046]
[0047] 5. Configuration of curing agent. Diethylenetriamine (DETA) was selected as the curing agent, and DETA was formulated into a 10mol / L aqueous solution to obtain liquid B.
[0048] 6. Configuration of c...
Embodiment 3
[0053] 1. Configuration of silane mixture. Mix and stir the silane KH-560 and TEOS at a molar ratio of n(KH560):n(TEOS)=2:0.8 to obtain a silane mixture.
[0054] 2. Configuration of hydrolysis catalyst. Acetic acid and phytic acid are uniformly mixed in a molar ratio of n(acetic acid):n(phytic acid)=2.4:1.2 to obtain a hydrolysis catalyst.
[0055] 3. Co-solvent configuration. Co-solvent is selected ethanol.
[0056] 4. Configuration of hydrolysis reaction. At room temperature, mix the silane mixed solution, hydrolysis catalyst, co-solvent and deionized water according to the following parts by weight, continue to stir, and hydrolyze for 3 to 4 days until the mixed solution is clear, then age it for later use to obtain liquid A.
[0057]
[0058] 5. Configuration of curing agent. The curing agent is triethylenetetramine (TETA), and TETA is made into a 10mol / L aqueous solution to obtain liquid B.
[0059] 6. Configuration of cross-linking reaction. At room temperatur...
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