Synthetic method and applications of modified polyaspartic acid with Schiff base structure
A technology of polyaspartic acid and synthesis method, which is applied in the field of modified polyaspartic acid corrosion inhibitors, can solve the problems of poor corrosion inhibition performance and no published modified polyaspartic acid corrosion inhibitors, etc. To achieve the effect of protection from corrosion
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Embodiment 1
[0021] First, maleic anhydride and ammonia are used for thermal condensation reaction to produce polysuccinimide. Polysuccinimide is ring-opened by thiocarbazide amino under NaOH alkaline conditions to obtain an intermediate product, and then the intermediate product and p-chlorobenzaldehyde Aldamine condensation reaction, glacial acetic acid as a catalyst, water phase reaction.
[0022] Synthesis of modified polyaspartic acid with Schiff base structure
[0023] 9.802g (0.1moL) maleic anhydride was dissolved in a 250mL three-necked flask filled with 10ml of distilled water and placed in a 70°C water bath with heating and stirring for 10min.
[0024] Take 9mL of ammonia water (0.1moL) into the funnel, slowly add it to the above three-necked flask within 2min, after the dripping is completed, raise the temperature to 75℃, react at a constant temperature for 1h, then pass argon into the flask as a protective gas, and the oil bath heats up When the temperature reaches 180°C, the polymer...
Embodiment 2
[0038] The other steps are the same as in Example 1. The difference is that the thermal polycondensation reaction of maleic anhydride and ammonia water produces polysuccinimide. The polymerization time is 40 minutes. The performance test results are shown in Table 2.
[0039] Table 2
[0040] PASP / SB concentration (mg / L)
[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] The other steps are the same as in Example 1, except that 1g PSI and 1.5g thiocarbazide are dissolved in a 100mL single-neck flask filled with 30mL distilled water. The performance test results are shown in Table 3
[0044] table 3
[0045] PASP / SB concentration (mg / L)
[0046] Example 3 is the effect of the grafting rate of the intermediate product PASP-CD on the corrosion inhibition performance of modified polyaspartic acid with a Schiff base structure.
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