Synthesis method for amphoteric ion modified starch for well drilling fluid
A technology of zwitterions and synthetic methods, which is applied in drilling compositions, chemical instruments and methods, sulfonate preparation, etc., can solve the problem of inability to achieve the "reverse polyelectrolyte" effect, and the imbalance between polymer hydration performance and inhibition performance , Salt and calcium resistance of polymers, etc.
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Embodiment 1
[0025] First prepare methacryloyloxyethyl-N,N-dimethylpropanesulfonate (DMAPS)
[0026] Weigh 630gDM and put it into the reactor, then put it into the constant temperature water bath, heat and start stirring. Then weigh 122g PS, add it directly into DM, the reaction temperature is 35°C, stir and react for 1.5h to get the crude product of DMAPS. Transfer the crude DMAPS product to a large piece of filter paper, wrap it in a Soxhlet extractor, and use ethanol as a solvent to extract it for 1 hour. After the extraction, put the filter paper bag in a drying oven and dry it at 40°C to obtain The pure DMAPS monomer has a yield of 92.8%, (the yield is the ratio of the mass of the product actually obtained and the mass of the theoretical product obtained by the stoichiometric reaction).
Embodiment 2
[0032] Weigh 100g of starch and add deionized water to gelatinize at 60°C for 30min, 2 After 30min, add 5g of potassium persulfate, weigh 100g of AM and 170g of DMAPS in deionized water to dissolve and transfer to the gelatinized starch reactor. The total mass concentration of the monomer is 25%. Washing yielded a white precipitate. The white precipitate was dried at 70°C for 12 hours and crushed to obtain the final product.
Embodiment 3
[0034]Weigh 100g of starch and add deionized water to gelatinize at 60°C for 30 min, 2 After 30 min, add 3 g of potassium persulfate, weigh 80 g of AM and 150 g of DMAPS in deionized water to dissolve and transfer to the gelatinized starch reactor. The total mass concentration of the monomer is 20%. Washing yielded a white precipitate. The white precipitate was dried at 70°C for 12 hours and crushed to obtain the final product.
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