Propylene gas-phase epoxidation catalyst used at ordinary pressure and preparation method of catalyst
A catalyst and epoxidation technology, applied in the direction of metal/metal oxide/metal hydroxide catalyst, physical/chemical process catalyst, chemical instrument and method, etc., can solve the problem of high reaction pressure, achieve high activity and save energy and cost, cost reduction effect
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Embodiment 1
[0020] Example 1: Bi 2 SiO 5 / SiO 2 Synthesis of carrier: publication number CN101229510A discloses a bismuth-containing bismuth silicate (Bi) with mesoporous characteristics synthesized by hydrothermal method 2 SiO 5 ) Catalytic material, carrier Bi 2 SiO 5 / SiO 2Synthesize according to its synthesis steps.
[0021] Catalyst Fe 2 o 3 -MoO 3 -Bi 2 SiO 5 / SiO 2 Preparation of (Si / Bi=50, Mo / Bi=2, Fe / Mo=0.1): Weigh about 80 g of the above Bi 2 SiO 5 / SiO 2 The carrier was dispersed by adding 500 ml of deionized water, and stirred in an ice-water bath for 0.5 h; 1.82 g of ferric ammonium EDTA was weighed and dissolved in 500 mL of deionized water according to the molar ratio Fe / Mo=0.1, and added dropwise to Add the above carrier powder slurry, and continue stirring for 0.5 h in an ice-water bath environment; then weigh 8.08 g of molybdic acid according to the molar ratio Mo / Bi=2, dissolve it in 500 mL deionized water, add it dropwise to the above slurry, and Stir i...
Embodiment 2
[0023] Embodiment 2: as the catalyst system of embodiment 1, but according to Mo / Bi=5, the mol ratio of Fe / Mo=0.2 prepares catalyst Fe 2 o 3 -MoO 3 -Bi 2 SiO 5 / SiO 2 , and the molybdenum precursor is ammonium paramolybdate, and the iron precursor is ferric ammonium citrate; the stirring condition for loading the active component is -10 ℃ for 2 h, and the ultrasonic impregnation condition is -10 ℃ for 2 h with ultrasonic vibration. The obtained samples were dried at 80 °C for 5 h, ground and calcined at 400 °C for 15 h, and other reaction conditions were the same as in Example 1. The results of the epoxidation reaction are shown in Table 1.
Embodiment 3
[0024] Example 3: The catalyst system as in Example 1, but the iron precursor is iron acetylacetonate. When loading the active components, the stirring condition is 20 °C for 8 h, and the ultrasonic impregnation condition is 20 °C ultrasonic vibration impregnation for 10 h, the impregnated The resulting slurry was dried at 120 °C for 20 h, and the resulting particles were calcined at 550 °C for 8 h after drying. When evaluating the epoxidation activity, the reaction temperature was 400°C, the pressure was 0.2 MPa, air was used as the oxygen source, and the air purity was greater than 99.9%. Fujian Xinhang Industrial Gas Co., Ltd., and other reaction conditions were the same as in Example 1. The results of the epoxidation reaction are shown in Table 1.
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