Hydrophobic monomer and hydrogen for drilling leaking stoppage based on monomer
A hydrophobic monomer and alkenyl amide technology, applied in the field of petroleum additives, can solve the problems of plugging failure, repeated leakage, poor deformability, etc.
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Embodiment 1
[0061] Preparation of hydrophobic monomer
[0062] In a dry three-necked flask with a stirrer, a condenser and a dropping funnel, 2850 mL of xylene and 66.04 g of compound II (m=10) were added, and 114.45 g of isophorone diisocyanate was added to the dropping funnel. Stir until the compound II in the flask is fully dissolved. Then the water bath was heated to a temperature of 54°C, and vacuum was applied for 2.0 hours while heating to remove water. Under the protection of nitrogen, add 0.08 g of dibutyl tin dilaurate. The isophorone diisocyanate in the dropping funnel was dropped into the three-necked flask, and the reaction was carried out for 3.5 hours under stirring. Then, the reaction temperature was raised to 65° C., and under the protection of nitrogen, 0.0572 g of dibutyl tin dilaurate and 50.55 g of N-methylol acrylamide were added respectively, and the reaction was continued for 4.5 hours with stirring. After the reaction, the acetone was distilled off under reduced p...
Embodiment 2
[0064] Preparation of hydrogel
[0065] 14.22g of acrylamide, 32.43g of sodium methacrylate, 22.93g of sodium 2-acrylamide-2-methylpropanesulfonate and 800mL of water were sequentially added into the reactor, and stirred until completely dissolved. Then, 2.96g of the hydrophobic monomer prepared in Example 1 and 36.35g of sodium dodecylbenzene sulfonate were added, and stirring was continued to solubilize the hydrophobic monomer in the micelles of sodium dodecylbenzene sulfonate. Nitrogen was applied for 30 minutes. Vent the air. Add 0.7254g(NH 4 ) 2 S 2 O 8 , And the temperature is increased to 40°C under the condition of continuous nitrogen flow, and the reaction is continued for 12 hours to obtain a colloidal product. The target product can be obtained by washing with absolute ethanol, crushing, and drying.
Embodiment 3
[0067] Preparation of hydrogel
[0068] 34.70g of N,N-dimethylacrylamide, 47.02g of sodium acrylate, 30.93g of sodium p-styrene sulfonate and 2140mL of water were sequentially added into the reactor, and stirred until completely dissolved. Then add 9.84 g of the hydrophobic monomer prepared in Example 1 and 46.18 g of sodium octadecyl benzene sulfonate, continue to stir to solubilize the hydrophobic monomer in the micelles of sodium octadecyl benzene sulfonate, and blow nitrogen for 30 minutes. Vent the air. Add 1.68g(NH 4 ) 2 S 2 O 8 , And under the condition of continuous nitrogen flow, the temperature is raised to the predetermined reaction temperature of 55 DEG C, and the reaction is continued for 8 hours to obtain a colloidal product. The target product can be obtained by washing with absolute ethanol, crushing, and drying.
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