Polymer clay stabilizer containing Beta-cyclodextrin structure and synthesis method thereof
A clay stabilizer and polymer technology, applied in the field of polymer clay stabilizer and its synthesis, can solve the problems of inability to produce multi-point adsorption, resistance to erosion, formation transformation, etc., and achieve rigidity enhancement, viscosity increase, and inhibition of hydration. the effect of expansion
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Embodiment 1
[0020] Embodiment 1: the preparation of XBH monomer
[0021] Add 100ml of deionized water and 1.5g of sodium hydroxide to a single-necked flask to make a 1.5% alkali solution, after cooling down, add 34.05g (0.03mol) β - After the cyclodextrin was stirred until it became clear, 3.4242 g (0.03 mol) AGE was added dropwise at room temperature for 5 minutes and reacted for 7 hours. After the reaction, neutralized with 85% phosphoric acid and filtered under reduced pressure to remove unreacted β -cyclodextrin, the filtrate was dissolved with ethanol and centrifuged to separate the salt, and the supernatant was distilled under reduced pressure to obtain a light yellow viscous liquid XBH.
Embodiment 2
[0022] Example 2: Synthesis of AM / NaAA / AMPS / XBH Tetrapolymer
[0023]First weigh AA and AMPS according to the ratio in Table 1, put them into a 250mL jar and dissolve them with distilled water, cool to room temperature, add AM and XBH, and dissolve them completely at room temperature, adjust the pH to 7 with NaOH solution, and blow nitrogen 20min, add the pre-prepared sodium bisulfite solution, stir for 5min, then add ammonium persulfate solution, continue to pass nitrogen for 10min, at a constant temperature of 35 o C under sealed reaction 8h. Precipitate with absolute ethanol, crush the precipitate into particles, soak it in absolute ethanol at 40 o C drying for 2 days to obtain AM / NaAA / AMPS / XBH tetrapolymer:
[0024] Table 1 Quaternary polymer synthesis drug dosage
[0025]
Embodiment 3
[0026] Example 3: Structural characterization of AM / NaAA / AMPS / XBH tetrapolymer
[0027] The infrared spectrograms of monomer XBH and tetrapolymer AM / NaAA / AMPS / XBH synthesized by embodiments 1 and 2 are as follows figure 1 shown. In the monomer XBH spectrum, 3342.03cm -1 -OH stretching vibration peak at 1675.84cm -1 and 1602.56cm -1 It is the characteristic peak of -C=C-, 1427.07cm -1 、1353.78cm -1 、1282.43cm -1 everywhere is β- The characteristic peak of cyclodextrin ring, 1151.29cm -1 、1081.87cm -1 and 1035.59cm -1 is the characteristic peak of ether bond. From the polymer spectrum in the figure, –OH and –NH 2 The stretching vibration peak is at 3427.88cm -1 (compared with 3342.03 in XBH, the peak is broadened, so –OH and –NH 2 overlap), –C=O stretching vibration peak at 1675.84cm -1 , 1451.92cm -1 、1407.78cm -1 and 1324.86cm -1 everywhere is β- The characteristic peak of the cyclodextrin ring, –SO 3 - Stretching vibration peak at 1191.79cm -1 place.
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