Method for preparing cyclic carbonate by transforming copper-based catalyst into carbon dioxide
A technology of cyclic carbonate and copper-based catalysts, applied in chemical instruments and methods, physical/chemical process catalysts, organic compounds/hydrides/coordination complex catalysts, etc., can solve the problems of low efficiency and save energy , short response time, and reduced pressure equipment requirements
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Embodiment 1
[0020] The copper-based catalyst of the present embodiment converts carbon dioxide to prepare the method for cyclic carbonate, the steps are as follows:
[0021] Into a 10mL stainless steel autoclave, sequentially add 50mg (active component copper 0.5mol%) catalyst conjugated copper porphyrin microporous polymer material, 12.5mmol propylene oxide and 0.9mmol cocatalyst tetra-n-butyl bromide Ammonium, feed carbon dioxide and keep the pressure at 0.1MPa, stir at 25°C for 48 hours, cool at room temperature, slowly release the remaining carbon dioxide, filter and separate the catalyst, and obtain the isolated yield of cyclic carbonate after purification 92%.
Embodiment 2
[0023] The copper-based catalyst of the present embodiment converts carbon dioxide to prepare the method for cyclic carbonate, the steps are as follows:
[0024] Into a 10mL stainless steel autoclave, add 50mg (active component copper 0.2mol%) of catalyst-conjugated copper porphyrin microporous polymer material, 12.5mmol of butylene oxide and 0.9mmol of cocatalyst tetra-n-butyl bromide ammonium chloride, feed carbon dioxide and keep the pressure at 0.1 MPa, stir at 25°C for 48 hours, cool at room temperature, slowly release the remaining carbon dioxide, filter and separate the catalyst, and obtain the isolated product of cyclic carbonate after purification The rate is 90%.
Embodiment 3
[0026] The copper-based catalyst of the present embodiment converts carbon dioxide to prepare the method for cyclic carbonate, the steps are as follows:
[0027] Into a 10mL stainless steel autoclave, add 50mg (active component copper 0.4mol%) of catalyst-conjugated copper porphyrin microporous polymer material, 12.5mmol epichlorohydrin and 0.9mmol cocatalyst tetra-n-butyl bromide ammonium chloride, feed carbon dioxide and keep the pressure at 0.1 MPa, stir at 25°C for 48 hours, cool at room temperature, slowly release the remaining carbon dioxide, filter and separate the catalyst, and obtain the isolated product of cyclic carbonate after purification The rate is 92%.
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