A novel hydrate kinetic inhibitor and its preparation method
A technology of kinetic inhibitor and hydrate inhibitor, which is applied to chemical instruments and methods, drilling compositions, etc., can solve the problems of unsatisfactory inhibitory effect, loss of inhibitory effect, limited application range, etc., and achieve good inhibitory effect. , the effect of reducing the generation rate, wide applicability
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Embodiment 1
[0028] Embodiment 1: The hydrate kinetics inhibitor (referred to as PVPSCH for short) as shown in formula II 2 COOH) synthesis
[0029]
[0030] Among them, the average value of n is 478.
[0031] The synthetic method comprises the following steps: Weigh 352mg (2mmol) of the chain initiator azobisisobutyronitrile into a 250mL eggplant-shaped reaction bottle, seal it with a rubber stopper, and then vacuumize and blow nitrogen three times; slowly add N-vinylpyrrole oxalanone monomer 20mL (206mmol), mercaptoacetic acid 0.56mL (about 5mmol) and N,N-dimethylformamide solvent 100mL, use liquid nitrogen to freeze-pump-heat cycle 3 times; Reaction at high temperature for 7 hours; the obtained initial product was cooled to room temperature and then slowly dripped into 1000mL cold ethyl acetate for recrystallization, suction filtration, and the obtained solid was dried in a vacuum oven at 45°C for 48 hours and then dried at 105°C After drying for 1 hour, the target product was obta...
Embodiment 2
[0034] Embodiment 2: The hydrate kinetic inhibitor (PVPSCH 2 CH 2 COOH) synthesis
[0035]
[0036] Among them, the average value of n is 1665.
[0037]The synthesis method comprises the following steps: Weigh 176mg (1mmol) of the chain initiator azobisisobutyronitrile into a 100mL eggplant-shaped reaction bottle, seal it with a rubber stopper, and then vacuumize and blow nitrogen for 3 times; slowly add N-vinylpyrrole 11mL of oxalanone monomer, 0.28mL of 3-mercaptopropionic acid (about 2.5mmol) and 50mL of N,N-dimethylformamide solvent, freezing with liquid nitrogen-pumping-heating cycle 3 times; ℃ for 12 hours; the obtained primary product was cooled to room temperature and then slowly dripped into 400mL of cold ethyl acetate for recrystallization and suction filtration. Drying under high temperature for 1 hour, the target product was obtained. The weight average molecular weight (Mw) is 184908, its 13 CNMR spectrum (D 2 O as a solvent) such as Figure 4 As shown, ...
Embodiment 3
[0038] Embodiment 3: inhibition effect evaluation
[0039] The method for inhibiting effect evaluation of the present invention is as follows:
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