Silicon-containing zwitterionic coating inhibitor and preparation method thereof
A technology of coating inhibitors and zwitterions, which is applied in the field of silicon-containing zwitterionic coating inhibitors and its preparation, can solve the difficulty of performance control, the difficulty of rheological stability control of drilling fluid, and the increase of drilling fluid system. Viscosity and other issues can be improved to improve the adsorption strength and capacity, which is beneficial to field application and has a good coating inhibition effect
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Embodiment 1
[0015] Mix 40.00g of acrylamide, 50.00g of sodium acrylate, 8.00g of diallyldimethylammonium chloride, 2.00g of methyl vinyl chlorosilane, 0.5g of alkyl polyoxyethylene ether and 233.33g of water, stir and dissolve to form The monomer solution is ready for use; add 120.00g cyclohexane and 0.20g sorbitan monolaurate dispersant to the four-necked flask, stir and dissolve; take 13.35g of the prepared monomer solution, and gradually add it dropwise until the oil is filled with In the flask with the same phase, a reverse phase suspension was formed, and 0.003g potassium persulfate was added, heated to 50°C under a nitrogen atmosphere and kept for self-reaction for 1 hour. When the water phase does not increase significantly, the azeotropy is stopped, the temperature is lowered and the obtained polymer particles are filtered out, and the sample is obtained after vacuum drying at 80°C.
Embodiment 2
[0017] Mix 60.00g of acrylic acid, 30.00g of potassium methacrylate, 5.00g of diallyldimethylammonium chloride, 5.00g of vinyltrichlorosilane, 1.00g of sodium dodecylbenzenesulfonate and 66.67g of water, and stir Dissolve to form a monomer solution for later use; add 100.00g cyclohexane and 4.00g polyoxyethylene sorbitan monooleate dispersant to the four-neck flask, stir and dissolve; take 69.33g of the prepared monomer solution, and gradually add Put it into the flask with the oil phase to form a reverse phase suspension, add 0.42g of azobisisobutylamidine hydrochloride, heat to 45°C under nitrogen atmosphere and keep self-reaction for 4 hours. Boil off the water, and when the water phase in the lower layer of the water separator no longer increases significantly, stop the azeotropy, cool down and filter out the obtained polymer particles, and vacuum-dry at 80°C to obtain a sample.
Embodiment 3
[0019] Mix 50.00g of acrylamide, 32.00g of potassium acrylate, 8.00g of diallyldimethylammonium chloride, 10.00g of vinyl trichlorosilane, 2.00g of alkylphenol polyoxyethylene ether OP-10 and 150.00g of water, Stir and dissolve to form a monomer solution for later use; add 100.00 g of cyclohexane, 1.00 g of polyoxyethylene sorbitan monooleate and 1.00 g of sorbitan monolaurate dispersant to a four-neck flask, and stir to dissolve; Take 51.00g of the prepared monomer solution, and gradually add it dropwise to the flask with the oil phase to form a reverse phase suspension, and add 0.10g of ammonium persulfate, heat to 55°C under nitrogen atmosphere, and then keep self-reaction for 2 hours After the reaction, the water was removed by vacuum azeotropy, and when the water phase in the lower layer of the water separator no longer increased significantly, the azeotropy was stopped, the temperature was lowered and the obtained polymer particles were filtered out, and the sample was ob...
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