CO2 responsive polymer microsphere based on interpenetrating network structure and preparation method of CO2 responsive polymer microsphere
An interpenetrating network structure and polymer technology, applied in the field of CO2 responsive polymer microspheres and their preparation, can solve problems such as inhibiting response performance, and achieve the effects of high yield, mild reaction conditions and simple operation.
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Embodiment 1
[0035] (1) Dissolve 12.30 g of acrylamide and 0.61 g of cross-linking agent methylenebisacrylamide (the cross-linking degree is 4.9 wt%) in deionized water to obtain solution I, and dissolve 0.1 g of initiator AIBI in deionized water to obtain a solution Ⅱ. At room temperature, pass nitrogen gas into the two solutions to remove oxygen for 0.5h. Dissolve 0.5g of emulsifier Span-60 in cyclohexane to obtain emulsifier solution. 2 Under protection, deoxygenated solution I and solution II were added dropwise to the emulsifier solution simultaneously. After solution I and solution II were added dropwise, the N 2 Protect, stir and react at 60°C for 6 hours, isolate the microspheres obtained after the reaction, alternately wash the microspheres with ethanol and deionized water to remove impurities, and then vacuum dry to obtain the skeleton polymer microspheres (polyacrylamide microspheres);
[0036] (2) Mix 1.05g of the skeleton polymer microspheres obtained in step (1) with 2.8g of ...
Embodiment 2
[0038] (1) Dissolve 12.30 g of acrylamide and 0.025 g of cross-linking agent methylenebisacrylamide (the cross-linking degree is 0.2 wt%) in deionized water to obtain solution I, and dissolve 0.1 g of initiator AIBI in deionized water to obtain For solution II, pass nitrogen gas into the two solutions at room temperature to deoxygenate for 0.5h, dissolve 0.5g of emulsifier Span-60 in cyclohexane to obtain emulsifier solution, and store in N 2Under protection, deoxygenated solution I and solution II were added dropwise to the emulsifier solution simultaneously. After solution I and solution II were added dropwise, the N 2 Protect, stir and react at 60°C for 6 hours, isolate the microspheres obtained after the reaction, alternately wash the microspheres with ethanol and deionized water to remove impurities, and then vacuum dry to obtain the skeleton polymer microspheres (polyacrylamide microspheres);
[0039] (2) After mixing 1.05g of skeleton polymer microspheres obtained in st...
Embodiment 3
[0041] (1) Dissolve 12.30 g of acrylamide and 0.12 g of cross-linking agent methylenebisacrylamide (the cross-linking degree is 0.97 wt%) in deionized water to obtain solution I, and dissolve 0.1 g of initiator AIBI in deionized water to obtain For solution II, pass nitrogen gas into the two solutions at room temperature to deoxygenate for 0.5h, dissolve 0.5g of emulsifier Span-60 in cyclohexane to obtain emulsifier solution, and store in N 2 Under protection, deoxygenated solution I and solution II were added dropwise to the emulsifier solution simultaneously. After solution I and solution II were added dropwise, the N 2 Protect, stir and react at 60°C for 6h, isolate the microspheres obtained after the reaction, alternately wash the microspheres with ethanol and deionized water to remove impurities, and then vacuum dry to obtain the skeleton polymer microspheres (polyacrylamide microspheres). Infrared spectrum see figure 2 ;
[0042] (2) 1.05 g of the skeleton polymer mic...
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