Solid alkali catalyst, preparation and use thereof
A solid base catalyst and solvent technology, which is applied in the direction of catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems such as low product yield, difficult catalyst regeneration, and difficult separation of homogeneous catalysts. Reduce operating units, eliminate adverse effects, and greatly promote the effect of the process
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Embodiment 1
[0042] Embodiment 1: the preparation of solid particle type solid base SX1
[0043] Under stirring, 7.86 g of calcium nitrate tetrahydrate was dissolved in 400 ml of ethanol, and stirring was continued for 30 minutes. 200 ml of deionized solution dissolved with 3.51 g of sodium carbonate was slowly added dropwise to the above solution, the precipitate was centrifuged, washed 4 times with deionized water, and then dried in an oven at 110° C. for 24 hours. The obtained sample was calcined at 1200° C. for 0.5 hour to obtain solid particle type solid base SX1. SX1 has a particle size of 400 microns.
Embodiment 2
[0044] Embodiment 2: the preparation of solid particle type solid base SX2
[0045] Under stirring, 7.86 g of calcium nitrate tetrahydrate was dissolved in 15.72 ml of deionized water and stirring was continued for 60 minutes. 200 ml of deionized solution dissolved with 10.55 g of sodium carbonate was slowly added dropwise to the above solution, centrifuged to separate the precipitate, washed 4 times with deionized water, and then placed in an oven at 110° C. for 24 hours to dry. The obtained sample was calcined at 700° C. for 10 hours to obtain solid particle type solid base SX2. SX2 has a particle size of 280 microns.
Embodiment 3
[0046] Embodiment 3: the preparation of solid particle type solid base SX3
[0047] Under stirring, 8 g of calcium nitrate tetrahydrate, 1.14 g of potassium nitrate and 0.66 g of sodium chloride were dissolved in 400 ml of ethanol and stirring was continued for 30 minutes. 200 ml of deionized solution dissolved with 15 g of sodium carbonate was slowly added dropwise to the above solution, centrifuged to separate the precipitate, washed with deionized water for 4 times, and then placed in a Dewar flask at -20°C to dry at low temperature for one week. The obtained solid sample was calcined at 850° C. for 4 hours to obtain solid particle type solid base SX3. SX3 has a particle size of 320 microns.
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