Composite-oxide catalyst and process for production of acrylic acid using said catalyst
A composite oxide and catalyst technology, which is applied in the preparation of organic compounds, metal/metal oxide/metal hydroxide catalysts, carbon-based compounds, etc. Excellent effect with excellent catalyst life
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[0029] That is, other acrylic acid production methods mentioned in the present invention are acrylic acid production methods including the following steps: introducing a mixed gas containing high concentrations of propylene and oxygen and practically no steam into a tank filled with molybdenum and Step (1) of preparing acrolein-containing gas in a fixed-bed multi-tubular first reactor of a composite oxide catalyst having bismuth as an essential component, introducing the acrolein-containing gas into a reactor filled with molybdenum and vanadium In the fixed-bed multi-tubular second reactor of the composite oxide catalyst, the step (2) of preparing acrylic acid-containing gas, and the step of introducing the above-mentioned acrylic acid-containing gas into an acrylic acid absorption tower to form a high-concentration acrylic acid solution for trapping ( 3) It is characterized in that, as the composite oxide catalyst filled in the above-mentioned fixed-bed multi-tubular second re...
Embodiment 1
[0052] (Preparation of Fe-Mo precursor)
[0053] While heating and stirring 500 ml of pure water, 21.9 g of ammonium paramolybdate was dissolved therein. In addition, 33.4 g of iron nitrate was dissolved in 150 ml of pure water while heating and stirring. After mixing the obtained two solutions, the mixture was kept at a temperature of 80° C. for 1 hour while stirring, and then the water was removed, followed by heat treatment at 500° C. for 3 hours. The obtained solid matter was pulverized to a particle size of 100 μm or less to prepare a Fe—Mo precursor.
[0054] (catalyst preparation)
[0055] While heating and stirring 2000 ml of pure water, 328 g of ammonium paramolybdate, 96.6 g of ammonium metavanadate, and 53.5 g of ammonium paratungstate were dissolved therein. Moreover, while heating and stirring 200 g of pure water, 79.8 g of copper nitrate and 4.8 g of antimony trioxide were added. After mixing the two obtained solutions, add the pre-prepared Fe-Mo precursor, p...
Embodiment 2
[0068] (Preparation of Fe-Mo precursor)
[0069] While heating and stirring 500 ml of pure water, 87.5 g of ammonium paramolybdate was dissolved therein. In addition, 133 g of iron nitrate was dissolved in 150 ml of pure water while heating and stirring. After mixing the obtained two solutions, the mixture was kept at a temperature of 80° C. for 1 hour while stirring, and then the water was removed, followed by heat treatment at 500° C. for 3 hours. The obtained solid matter was pulverized to a particle size of 100 μm or less to prepare a Fe—Mo precursor.
[0070] (catalyst preparation)
[0071] While heating and stirring 2000 ml of pure water, 262.5 g of ammonium paramolybdate, 96.6 g of ammonium metavanadate, and 53.5 g of ammonium paratungstate were dissolved therein. Moreover, while heating and stirring 200 g of pure water, 79.8 g of copper nitrate and 4.8 g of antimony trioxide were added. After mixing the two obtained solutions, add the pre-prepared Fe-Mo precursor, ...
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