A kind of synthetic method and application of modified polyaspartic acid with Schiff base structure
A polyaspartic acid and synthesis method technology, applied in the field of modified polyaspartic acid corrosion inhibitors, can solve the problems of unpublished modified polyaspartic acid corrosion inhibitors, poor corrosion inhibition performance, etc.
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Embodiment 1
[0021] Firstly, polysuccinimide is generated by thermal polycondensation reaction of maleic anhydride and ammonia water, and polysuccinimide is subjected to ring-opening reaction of thiocarbazide amino group under NaOH alkaline conditions to obtain an intermediate product, and then the intermediate product is reacted with p-chlorobenzaldehyde Aldehyde-amine condensation reaction, glacial acetic acid as catalyst, water phase reaction.
[0022] Synthesis of Modified Polyaspartic Acid with Schiff Base Structure
[0023] Dissolve 9.802g (0.1moL) of maleic anhydride in a 250mL three-necked flask filled with 10ml of distilled water, and heat and stir in a 70°C water bath for 10min.
[0024] Take 9mL of ammonia water (0.1moL) in the funnel, and slowly add it into the above-mentioned three-neck flask within 2min. After the dropwise addition, raise the temperature to 75°C and react at a constant temperature for 1h. To 180°C, polymerize for 30 minutes, stop heating, and naturally cool ...
Embodiment 2
[0038] The other steps are the same as in Example 1, except that the polymerization time of maleic anhydride and ammonia water to generate polysuccinimide is 40 minutes, and the performance test results are shown in Table 2
[0039] Table 2
[0040] PASP / SB concentration (mg / L) Mass loss (g) Corrosion inhibition rate η(%) 0 0.2285 _ 10 0.0723 68.4 20 0.0604 73.6 40 0.0399 82.5 80 0.0221 90.3
[0041] Example 2 is the effect of the polymerization time of polysuccinimide on the corrosion inhibition performance of modified polyaspartic acid with Schiff base structure.
Embodiment 3
[0043] Other steps are the same as in Example 1, except that 1gPSI and 1.5g of thiocarbazide are dissolved in a 100mL single-necked flask with 30mL of distilled water, and the performance test results are shown in Table 3
[0044] table 3
[0045] PASP / SB concentration (mg / L) Mass loss (g) Corrosion inhibition rate η(%) 0 0.2285 _ 10 0.0687 69.9 20 0.0581 74.6 40 0.0398 82.6 80 0.0203 91.1
[0046] Example 3 is the effect of the grafting ratio of the intermediate product PASP-CD on the corrosion inhibition performance of the modified polyaspartic acid with Schiff base structure.
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