Corrosion inhibitor and preparation method
A technology of corrosion inhibitor and solvent, which is applied in the field of water-soluble corrosion inhibitor and its preparation, can solve the problems of corrosion inhibitor corrosion and achieve good corrosion inhibition performance
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Embodiment 1
[0018] Prepare the corrosion inhibitor according to the following steps:
[0019] Lauric acid and tetraethylenepentamine were reacted at 160°C for 3 hours, cooled to 50°C; added carbon disulfide, reacted at 40°C for 2 hours, added formaldehyde, stirred until no longer exothermic, added phosphorous acid, and heated to 80°C React for 1 hour to prepare modified imidazoline derivatives; wherein, the molar ratio of lauric acid, tetraethylenepentamine, carbon disulfide, formaldehyde and phosphorous acid is 1:1:1:1:0.5.
[0020] Add modified imidazoline derivatives, 1,4-butynediol, thiourea, sodium dodecylbenzenesulfonate, and urotropine to isopropyl in a mass ratio of 20:2:12:5:4 Among the alcohols, the mass content of isopropanol was 57%, and the corrosion inhibitor product A was obtained after stirring.
Embodiment 2
[0022] Prepare the corrosion inhibitor according to the following steps:
[0023] Lauric acid and polyethylene polyamine were reacted at 230°C for 5 hours, cooled to 60°C; added carbon disulfide, reacted at 70°C for 4 hours, added formaldehyde, stirred until no longer exothermic, added phosphorous acid, and heated to 90°C React for 2 hours to prepare modified imidazoline derivatives; wherein, the molar ratio of lauric acid, polyethylene polyamine, carbon disulfide, formaldehyde and phosphorous acid is 1:1.1:1:2:2.
[0024] Add modified imidazoline derivatives, 1,4-butynediol, thiourea, sodium dodecylbenzenesulfonate, and urotropine into water at a mass ratio of 50:1:1:1:2, and the water The mass content is 45%, and the corrosion inhibitor product B is obtained after stirring.
Embodiment 3
[0026] Prepare the corrosion inhibitor according to the following steps:
[0027] Oleic acid and polyethylene polyamine were reacted at 200°C for 4 hours, cooled to 55°C; added carbon disulfide, reacted at 60°C for 3 hours, added formaldehyde, stirred until no longer exothermic, added phosphorous acid, and heated to 85°C After reacting for 1.5 hours, a modified imidazoline derivative was obtained; wherein, the molar ratio of oleic acid, polyethylene polyamine, carbon disulfide, formaldehyde, and phosphorous acid was 1:1.05:1:1.5:1.
[0028] Add modified imidazoline derivatives, 1,4-butynediol, thiourea, sodium dodecylbenzenesulfonate, and urotropine to isopropanol in a mass ratio of 36:1.5:6.5:3:3 Among them, the mass content of isopropanol is 50%, and the corrosion inhibitor product C is obtained after stirring.
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