Molecular sieve catalyst, preparing method and use thereof
A molecular sieve and catalyst technology, applied in the field of modified molecular sieve catalyst, can solve the problems of reducing the economic benefit of aromatization, and achieve the effect of high reaction stability
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[0029] Example 1
[0030] Preparation of common catalyst:
[0031] 1) After calcining, the Na-type ZSM-5 molecular sieve (with a silicon-to-aluminum ratio of 55) and 30%wt SB powder (that is, styrene-butadiene, imported from Germany) are extruded and formed, dried, calcined, and then processed After ammonia exchange and roasting, the H-type molecular sieve catalyst used is obtained, and the catalyst is crushed into particles of 20-40 mesh before loading into the reactor, which is recorded as P.
[0032] 2) Place 5g of the catalyst obtained in step 1 in a continuous-flow fixed-bed reactor with an inner diameter of 10mm. The liquefied gas feedstock is heated at 350℃, 5atm, 2h -1 The catalyst was contacted under the condition of weight space velocity, and the reaction results are shown in Table 1.
[0033] Preparation of the catalyst of the present invention:
[0034] After calcination, 20g of Na-type ZSM-5 molecular sieve (with a silicon-to-aluminum ratio of 55) is placed in 1000ml,...
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[0039] Example 2
[0040] The above catalysts P and AT were treated with steam respectively, the steam treatment temperature was 530°C, the treatment time was 3h, and the resulting catalysts were denoted as P-530 and AT-530, respectively. Except that the reaction temperature was increased to 365°C, other reaction conditions were the same as in Example 1. The reaction results are shown in Table 2.
[0041] Cumulative response
[0042] It can be seen from Table 2 that the catalysts P and AT undergo high temperature hydrothermal treatment, and the modified catalyst AT-530 of the present invention shows better aromatization stability than P-530, and the amount of carbon deposit on the catalyst is still almost equal .
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