Method for producing mixed xylene by methylbenzene methylation
A technology of mixing xylene and methylation, which is applied in the direction of organic chemistry, condensation between hydrocarbons and non-hydrocarbons to produce hydrocarbons, etc. The effect of improving utilization rate, good technical effect, and improving catalyst life
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Embodiment 1
[0038] Take SiO 2 / Al 2 o 3 50g of hydrogen-type ZSM-5 molecular sieve with a molar ratio of 250, 21g of pseudoboehmite, and 1.5g of scallop powder were mixed for 20 minutes to obtain intermediate A. Take 15ml of nitric acid solution (mixing nitric acid with a mass concentration of 69% and water It is mixed according to the volume ratio of 1:1), and 1.4g magnesium oxide is dissolved in the nitric acid solution to obtain solution B, which is poured into A, kneaded and shaped, and roasted at 540°C for 5 hours to obtain a 1cm-long The strip catalyst C. C was treated with steam at 500°C for 2 hours to obtain a catalyst, which was designated as C1.
[0039] Four fixed bed reactors are connected in series. Each reactor adopts Φ2.54*60cm stainless steel tube, and is heated in three sections, and the temperature difference in the constant temperature section is less than ±1°C. The C1 catalyst is distributed in the constant temperature sections of four reactors, each reactor has t...
Embodiment 2
[0043] Adopt implementation 1 same method to prepare ZSM-5 molecular sieve catalyst, wherein SiO 2 / Al 2 o 3 The molar ratio is 350. Denote it as C2.
[0044] Get the C2 catalyst 40g and load the reactor in equal portions, and the reactor structure is the same as that of Example 1. The methylating reagent used was methanol. The number of reactors connected in series and the reaction conditions are shown in Table 1. The test results are shown in Table 2.
[0045]
Embodiment 3
[0047] Get C1 catalyst 40g and load the reactor in equal parts, and the reactor structure is identical with embodiment 1. The methylating agent used is dimethyl ether. The number of reactors connected in series and the reaction conditions are shown in Table 1. The test results are shown in Table 2.
[0048]
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