Acidizing corrosion inhibitor based on dimer indolizine derivative and preparation method and application of acidizing corrosion inhibitor
A technology of acidification corrosion inhibitor and indolezine, which is applied in the field of acidification corrosion inhibitor and its preparation, can solve problems such as application limitations, and achieve the effect of small influence, fast dissolution speed and good acid solubility
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Embodiment 1
[0038] Take pyridine and benzyl chloride with a molar ratio of 1:1, use the same molar amount of water as a solvent, heat and stir at 90-100°C for 8 hours, and obtain a dark yellow transparent liquid, which is a quaternary benzylpyridine chloride. Ammonium salt solution.
[0039] After the solvent water of the above-mentioned benzylpyridinium chloride quaternary ammonium salt solution is removed by heating and evaporating, N,N dimethylformamide is added as a solvent in the system, and triethylamine in an equimolar ratio with the initial raw material is added, and the process continues at 80 Heating and stirring at -100°C for 2 hours, benzylpyridinium chloride quaternary ammonium salt undergoes an intermolecular dimerization reaction to obtain a dimer indoleazine derivative, which is a dark brown liquid, evaporates and removes the solvent under heating, and becomes a corrosion inhibitor main agent.
[0040] The acidified corrosion inhibitor product can be obtained by mixing th...
Embodiment 2
[0042] Take quinoline and benzyl chloride with a molar ratio of 1:1, use the same molar amount of water as a solvent, heat and stir under reflux at 90-100°C for 6 hours, and obtain an orange-red transparent liquid, which is benzylquinoline chloride Quaternary ammonium salt solution.
[0043]After heating and evaporating the solvent water of the above-mentioned benzylquinoline quaternary ammonium salt solution, add acetonitrile to the system as a solvent, and add triethylamine in an equimolar ratio to the initial raw material, and continue heating and stirring at 80-100°C After 2 hours of reaction, benzylquinoline quaternary ammonium chloride undergoes an intermolecular dimerization reaction to obtain a dimer indolezine derivative, which is a dark brown liquid, and evaporates to remove the solvent under heating, which is the main agent of the corrosion inhibitor.
[0044] The acidified corrosion inhibitor product can be obtained by mixing the obtained main agent of corrosion in...
Embodiment 3
[0046] Take pyridine and ethyl α-bromoacetate with a molar ratio of 1:1, use the same molar amount of water as a solvent, heat and stir under reflux at 90-100°C for 4 hours, and obtain a dark yellow transparent liquid, which is brominated acetic acid Ethylpyridinium quaternary ammonium solution.
[0047] After heating and evaporating the solvent water of the above-mentioned bromoacetate-based pyridinium quaternary ammonium salt solution, add N,N dimethylformamide as a solvent to the system, and add triethylamine in an equimolar ratio to the initial raw material, and continue Heating and stirring reaction at 80-100°C for 2 hours, brominated ethyl acetate pyridinium quaternary ammonium salt undergoes intermolecular dimerization reaction to obtain dimer indoleazine derivatives, which are dark orange-red liquids, evaporate and remove the solvent under heating, It is the main agent of corrosion inhibitor.
[0048] The acidified corrosion inhibitor product can be obtained by mixing...
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