Catalyst for preparing isopropamide by aminating acetone as well as preparation method and application thereof
A technology for the production of isopropylamine and catalysts by acetone ammoniation, which is applied in the preparation of amino compounds, organic compounds, physical/chemical process catalysts, etc. It can solve the problems of poor selectivity and low conversion rate, and achieve high repeatability and high conversion The effect of high efficiency and simple preparation steps
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Embodiment 1
[0037]Calculate and weigh a certain amount of nickel nitrate dissolved in water to prepare a solution according to the active component content of the load. The volume of the solution is equal to the volume of the liquid absorbed by the alumina carrier. The alumina carrier is impregnated by an equal volume impregnation method (by Beijing Chemical Industry Research Institute). Production) 1-2 hours, drying at 120°C for 2-4 hours. Next, the saturated aqueous solution of ammonium bicarbonate is impregnated to obtain alumina supporting 5-20 wt% nickel. The active component nickel can be impregnated in steps. The above catalyst is loaded into the reactor and reduced by introducing hydrogen at 200-500° C. for 8-10 hours to obtain the isopropylamine catalysts A-1, A-2 and A-3 of the present invention. The specific data of catalysts A-1, A-2 and A-3 are listed in Table 1.
Embodiment 2~6
[0047] Examples 2 to 6 evaluated catalysts A-1, A-2, A-3, B-1 and B-2, respectively.
[0048] The catalyst was evaluated using a fixed bed reactor. The amount of catalyst used for each evaluation was 50 ml. The starting materials and reaction products were analyzed using an Agilent 6890A gas chromatograph.
[0049] Using acetone as raw material, the reaction conditions are: normal pressure, reaction temperature of 110 °C, and volumetric space velocity of acetone solution of 0.5 h. -1 , Acetone: H 2 :NH 3 Molar ratio 1:3:3, under this reaction condition, carry out hydroamination reaction to produce isopropylamine, and the evaluation result is listed in Table 2.
[0050] Table 2 Catalyst evaluation results
[0051] catalyst
[0052] As can be seen from the data in Table 2, the catalyst of the present invention compared with the existing catalyst, the acetone conversion rate is high catalytic activity, the selectivity to isopropylamine is the high selectivity of th...
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