Method for preparing alternating copolymer of maleic anhydride and vinyl acetate
A vinyl acetate and alternating copolymer technology, applied in the field of copolymerization, can solve problems such as adverse effects on human body and environment, complex reaction system, etc., and achieve the effects of low cost, simple operation process and environmental friendliness
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Embodiment 1
[0019] in CO 2Under the atmosphere, add 100 g of mixed monomers of maleic anhydride and vinyl acetate with a molar ratio of 1:1.1 and 4 g of azobisisobutyronitrile (AIBN) into a 1 L reactor, and seal the reactor. The temperature of the reaction kettle was raised to 35°C, the pressure was raised to 7.5MPa, the temperature was raised to 55°C after pre-dissolving for 1 hour, the pressure reached 8MPa, and the reaction was carried out at constant temperature and pressure for 12 hours. Extract and purify 3 times under the supercritical state, finally open the pressure reducing valve to exhaust, and when the non-supercritical state is reached, turn off the heating device. When the pressure in the reactor is zero and the temperature is room temperature, open the reactor to take out the powdery product, put it into a desiccator for analysis and testing. Characterization by infrared, nuclear magnetic resonance and elemental analysis shows that the copolymer has an alternating structur...
Embodiment 2
[0021] The specific operation is the same as in Example 1, the total weight of the mixed monomers is 150g, the molar ratio is 1: 1.1, the initiator is benzoyl peroxide, the consumption is 0.075g, the temperature is 65°C, the pressure is 25MPa, and the reaction time is 24h. Characterization by infrared, nuclear magnetic resonance and elemental analysis shows that the obtained copolymer has an alternating structure, a weight-average molecular weight of 50,000, and a monomer conversion rate of 82.8%.
Embodiment 3
[0023] The specific operation is the same as in Example 1, the total weight of the mixed monomers is 250g, and the molar ratio is 1: 1.05. The initiator is azobisisoheptanonitrile, and the consumption is 2.5g. The reaction pressure is 20MPa, and the reaction temperature is 70°C. It is 18h. Characterization by infrared, nuclear magnetic resonance and elemental analysis shows that the obtained copolymer has a weight average molecular weight of 20,000 and a monomer conversion rate of 87.5%.
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