Water base drilling fluid, and preparation method and application thereof
A water-based drilling fluid and drilling fluid technology, applied in the field of drilling fluid, can solve the problems of high pollution, high cost, etc., and achieve the effect of enhancing the filtration loss reduction ability and strong inhibition
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Embodiment 1
[0038] Preparation of N,N-Dimethylallylaminopropanesulfonate
[0039] 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 93.7%.
Embodiment 2
[0045] Preparation of 4-vinylpyridinepropanesulfonate ylide (VPPS)
[0046] (1) Weigh 105g of 4-vinylpyridine (4-VP), 125g of 1,3-propane sultone (PS), 500g of organic solvent benzene, and 0.75g of diethylhydroxylamine;
[0047] (2) Divide the organic solvent benzene into three parts equally, dissolve and mix with 4-vinylpyridine, 1,3-propane sultone and auxiliary agent diethylhydroxylamine respectively;
[0048] (3) Add the obtained three mixed solutions into the reactor one by one, react at 70°C for 2h, then filter under reduced pressure, wash with benzene for 2-3 times, and dry at 50°C for 15h to obtain 4-ethylene Based on pyridyl propane sulfonate ylide (VPPS), 2136g of light yellow solid powder product was finally obtained after calculation.
Embodiment 3
[0050] Weigh 72g DAPS, 42g acrylamide (AM), 11g VPPS, add a certain amount of deionized water to dissolve and transfer to the reactor, the total monomer concentration is 25%. Access to N 2 Deoxygenation was performed for 1 hour, and the temperature was raised to 65° C., kept for 30 minutes, and then 1.3 g of potassium persulfate was added. After 6 hours of reaction, a gel-like solid was obtained, which was precipitated with acetone to obtain a white precipitate. After drying at 110°C for 24 hours, it was pulverized to obtain a zwitterionic copolymer.
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