Preparation method of cyclic carbonate by chromium-based catalyst
A cyclic carbonate, chromium-based catalyst technology, used in chemical instruments and methods, physical/chemical process catalysts, catalytic reactions, etc., can solve problems such as low efficiency, save energy, shorten reaction time, and reduce pressure equipment. desired effect
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Embodiment 1
[0020] The chromium-based catalyst of the present embodiment prepares the method for cyclic carbonate, the steps are as follows:
[0021] Into a 10mL stainless steel autoclave, add 50mg (active component chromium 0.4mol%) catalyst conjugated chromium porphyrin bipyridine microporous polymer material, 12.5mmol propylene oxide and 0.9mmol co-catalyst tetra-n-butyl in turn. Ammonium bromide, feed carbon dioxide and keep the pressure at 0.1MPa, stir for 48 hours at a temperature of 25°C, cool at room temperature, slowly release the remaining carbon dioxide, filter and separate the catalyst, and purify to obtain the separation of the cyclic carbonate Yield was 85%.
Embodiment 2
[0023] The chromium-based catalyst of the present embodiment prepares the method for cyclic carbonate, the steps are as follows:
[0024] Into a 10mL stainless steel autoclave, add 50mg (active component chromium 0.3mol%) catalyst conjugated chromium porphyrin bipyridine microporous polymer material, 12.5mmol butylene oxide and 0.9mmol co-catalyst tetra-n-butyl in turn. ammonium bromide, introduced carbon dioxide and kept the pressure at 0.1 MPa, stirred for 48 hours at a temperature of 25 °C, cooled at room temperature, slowly released the remaining carbon dioxide, separated the catalyst by filtration, and purified to obtain cyclic carbonate. The isolated yield was 83%.
Embodiment 3
[0026] The chromium-based catalyst of the present embodiment prepares the method for cyclic carbonate, the steps are as follows:
[0027] Into a 10mL stainless steel autoclave, add 50mg (active component chromium 0.5mol%) catalyst conjugated chromium porphyrin bipyridine microporous polymer material, 12.5mmol epichlorohydrin and 0.9mmol co-catalyst tetra-n-butyl in turn. ammonium bromide, introduced carbon dioxide and kept the pressure at 0.1 MPa, stirred for 48 hours at a temperature of 25 °C, cooled at room temperature, slowly released the remaining carbon dioxide, separated the catalyst by filtration, and purified to obtain cyclic carbonate. The isolated yield was 86%.
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