Method for preparing propylene by butylene-containing C4 fractioning hydrocarbon dismutation
A C4 fraction and butene technology, applied in the field of C4 fraction hydrocarbon disproportionation to propylene, can solve the problems of poor catalyst stability and high raw material composition requirements
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Embodiment 1
[0016] Take 4 grams of prepared MgO and 1 gram of WO 3 / SiO 2 Catalyst, wherein the specific surface area of MgO is 126.2 m 2 / gram, after mixing, put it into the constant temperature section of a reactor with a length of 110 centimeters and an internal diameter of 2.5 centimeters, and fill it with glass balls up and down. The catalyst bed is activated by the following method before feeding: feed air at a rate of 6 liters / hour, gradually heat up to 550°C, and keep at this temperature for 4 hours, then switch the air to nitrogen and keep the temperature for 8 hours, Lower the temperature to 300°C, raise the pressure to 3.0MPa with nitrogen, and stop feeding nitrogen. After the activation is completed, the molar ratio of butene and ethylene contained in the carbon four cut hydrocarbons is 1:2 to feed the carbon four cut hydrocarbons and polymer grade ethylene, and the weight space velocity in terms of butene is 1.2 hours -1 . The C4 distillate hydrocarbons are first purif...
Embodiment 2
[0022] According to the conditions and methods of Example 1, the C4 cut hydrocarbons are fixed as raw material B. a) Only change MgO and WO in the catalyst 3 / SiO 2 The weight ratio, the evaluation results are shown in Table 3; b) Only the type of alkaline earth metal in the catalyst is changed, and CaO is used instead of MgO, and the evaluation results are shown in Table 4.
[0023] The reaction result on the catalyst with different weight composition in table 3
[0024]
[0025] Table 4 Reaction results on different component catalysts
[0026]
Embodiment 3
[0028] According to the conditions and methods of Example 1, the C4 cut hydrocarbons were fixed as raw material B, and only the specific surface area of MgO was changed. The results are shown in Table 5.
[0029] The reaction result of magnesium oxide containing different specific surface areas in the catalyst of table 5
[0030]
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