Surface active ionic liquid bactericide and application thereof in sterilization of oilfield injection water
A technology of ionic liquid and surface activity, applied in application, biocide, disinfectant, etc., to achieve strong bactericidal and drug resistance, high surface activity, and mild conditions
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example 1
[0015] The preparation of example 1N-alkyl imidazoles
[0016] In a 100mL three-necked flask, add imidazole and potassium hydroxide, the molar ratio of the two is 1:1~1.2, and dimethyl sulfoxide (10~20mL) is used as a solvent, and the frequency is 30kHz, the power is 100w, and under the protection of nitrogen, In an ultrasonic reactor with a reaction temperature of 20-25°C, ultrasonication for 1 to 2 hours, cooling down to 0°C, and at this temperature, use a constant pressure dropping funnel to slowly drop bromoalkane ( 1-bromobutane, bromopentane, bromohexane), then heated up to 20-25°C, ultrasonically reacted for 3-4 hours, after the reaction, added 20-30mL distilled water to the reaction, extracted with 20-30mL chloroform , and then washed the chloroform layer with distilled water (4 × 20 ~ 30mL), the chloroform layer with anhydrous MgSO 4 After drying for 8-10 hours, the desiccant was removed by suction filtration, and the chloroform was distilled off from the filtrate un...
example 2
[0017] The preparation of example 2N-butyl-3-octyl (decyl, dodecyl, tetradecyl) imidazole surface-active ionic liquid
[0018] In a 100mL three-necked bottle with a drying device, add N-butylimidazole and bromooctane (bromodecane, bromododecane, bromotetradecane) respectively, and the molar ratio of the two is 1:1 ~2, nitrogen protection, start the ultrasonic reactor (ultrasonic frequency 40kHz, power 100w) for 25~35min, stop the ultrasonic for 5~10min intermittently, keep the water temperature at 60~70℃, react for 5~6h, and track the reaction by TLC. After the reaction was completed, it was washed with a mixed solvent of ethyl acetate and n-hexane (4×15-25 mL), and the remaining mixed solvent was evaporated to obtain a yellow viscous N-butyl-3-octyl (decyl, dodecyl , tetradecyl) imidazole surface-active ionic liquid.
[0019] N-butyl-3-octylimidazole surface active ionic liquid product 1 H-NMR (400MH Z , CDCl 3 , δ / ppmrelativetoTMS) verified as follows: 10.19 (1H, s, im...
example 3
[0023] Preparation of Example 3N-pentyl-3-octyl (decyl, dodecyl, tetradecyl) imidazole surface-active ionic liquid
[0024] In a 100mL three-neck flask with a drying device, add N-pentylimidazole and bromooctane (bromodecane, bromododecane, bromotetradecane) respectively, and the molar ratio of the two is 1:1 ~2, Nitrogen protection, start ultrasound (ultrasonic frequency 40kHz, power 100w) for 25-35min, stop intermittent ultrasound for 5-10min, keep the water temperature at 60-70℃, react for 5-6h, TLC tracking. After the reaction was completed, it was washed with a mixed solvent of ethyl acetate and n-hexane (4×15-25 mL), and the residual mixed solvent was evaporated to obtain a yellow viscous N-pentyl-3-octyl (decyl, dodecyl , tetradecyl) imidazole surface-active ionic liquid.
[0025] N-pentyl-3-octylimidazole surface active ionic liquid product 1 H-NMR (400MH Z , CDCl 3 , δ / ppmrelativetoTMS) verified as follows: 10.26 (1H, s, imidazole ring), 7.35 (2H, d, imidazole ri...
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