Method for preparing propylene by catalytic cracking olefin with four carbon or above
A catalytic cracking and olefin technology, applied in the production of bulk chemicals, hydrocarbon cracking to hydrocarbon production, organic chemistry, etc., can solve problems such as poor catalyst stability, and achieve the effect of improving stability, good resistance to carbon deposition and stability
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Embodiment 1~3
[0023] Molecular sieve silicon aluminum ratio has a significant impact on the stability of the catalyst. ZSM-5 molecular sieves with three silicon-aluminum ratios of A, B, and C were synthesized according to the ratio and crystallization conditions in Table 1.
[0024] Molecular sieve
[0025] 5 grams of ZSM-5 molecular sieve A was calcined at 600° C. for 10 hours in an air atmosphere. Then placed in 200 ml, 5% wt NH 4 NO 3 In the solution, exchange at a temperature of 85-90°C for 2 hours, and repeat 3 times. After the exchange, the hydrogen-type ZSM-5 molecular sieve was obtained by washing and drying at 120°C, and the catalyst A-1 was obtained. Catalyst B-1 and catalyst C-1 were prepared using molecular sieves B and C in the same manner.
Embodiment 4~5
[0027] C used in the experiment 4 The raw material comes from the raffinate mixed carbon four in the ethylene plant. The raw material composition is shown in Table 2.
[0028] project
Raw material composition (wt%)
1.81
n-butane
5.05
0.12
0.08
11.25
Butene-1
32.07
isobutene
43.39
maleic butene
6.20
C 4 above
0.04
[0029] Take 2 grams of catalyst A-1, activate the catalyst at 500°C under a nitrogen atmosphere for 2 hours before the reaction, and then use the raffinate mixed carbon four as raw material, at 500°C, the weight space velocity is 3 hours -1 The reaction is carried out under certain conditions. During the reaction, water is added to the raw material as a diluent gas, and the water / olefin weight ratio is 1.5. Take another 2 grams of B-1 catalyst, pre-reaction at 500 ° C, space velocity 3.0 hou...
Embodiment 7~9
[0032] Take 2 grams of A-1, B-1, and C-1 catalysts respectively, and pre-react at 500°C with a space velocity of 3.0 hours before the reaction -1 Under the water vapor atmosphere, after processing for 24 hours, A-2, B-2, and C-2 catalysts were prepared. Before the reaction, the catalyst was activated at 500°C under a nitrogen atmosphere for 2 hours, and then the residual mixed carbon four was used as raw material at 500°C with a weight space velocity of 3 hours -1 The reaction is carried out under certain conditions. During the reaction, water is added to the raw material as a diluent gas, and the water / olefin weight ratio is 1.5. The initial butene conversions of A-2, B-2, and C-2 after steam treatment were all greater than 75%. After a reaction time of 500 hours, the performance of the catalysts was compared.
[0033] Product distribution
[0034]It can be clearly seen from Table 2 that after the same time of reaction, the A-2 catalyst with the lowest silicon-alum...
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