Preparation method for amphoteric ion modified starch for well drilling fluid
A zwitterion and drilling fluid technology, which is applied in the direction of drilling compositions, chemical instruments and methods, etc., can solve the constraints of polymer salt and calcium resistance, the imbalance between polymer hydration performance and inhibition performance, and the inability to achieve "reverse" Polyelectrolyte effect and other issues
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Embodiment 1
[0024] First prepare N,N-dimethylallyl propane sulfonate.
[0025] Weigh 430g of N,N-dimethylallylamine (DA) into the reactor, then put it into a constant temperature water bath, heat and start stirring. Then weigh 122g of 1,3-propane sultone (PS), add it directly into DA, the reaction temperature is 45°C, stir and react for 3 hours to obtain N,N-dimethylallyl propane sulfonate (DAPS) crude products. Transfer the crude DAPS product to a large piece of filter paper, wrap it in a Soxhlet extractor, and use ethanol as a solvent to extract for 3 hours. After the extraction, put the filter paper bag in a drying box and dry it at 50°C to obtain Pure DAPS monomer with a yield of 94.3%.
Embodiment 2
[0031] Weigh 100g of starch and add deionized water to gelatinize at 60°C for 30min, 2 Add 5g potassium persulfate after processing for 30min, weigh 100g AM respectively, add 170g DAPS into deionized water for dissolving, then transfer to the gelatinized starch reactor, the total mass concentration of monomer is 25%, after reacting for 5h, a colloidal solid is obtained, and the Washing with acetone gave a white precipitate. The white precipitate was dried at 70° C. for 12 h and crushed to obtain the final product.
Embodiment 3
[0033] Weigh 100g of starch and add deionized water to gelatinize at 60°C for 30min, 2Add 3g potassium persulfate after processing for 30min, weigh 80g AM respectively, add 150g DAPS into deionized water to dissolve and then transfer to gelatinized starch reactor, the total mass concentration of monomer is 20%, after reacting for 6h, a colloidal solid is obtained, and Washing with acetone gave a white precipitate. The white precipitate was dried at 70° C. for 12 h and crushed to obtain the final product.
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