Regeneration method of deactivated catalyst
A deactivated catalyst and catalyst technology, applied in catalyst regeneration/reactivation, molecular sieve catalysts, chemical instruments and methods, etc., can solve problems such as difficult separation of macromolecular by-products, molecular sieve structure damage, metal platinum accumulation, etc. Hydrogen/dehydrogenation reactivity, improvement of dispersion, effects of avoiding damage
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Embodiment 1
[0031] Preparation of Catalyst E-1 of the Invention.
[0032] Add 1450ml of organic solution into a 2000ml flask (the volume ratio of ethanol and benzene is 2:1), and deactivate the Pt / ZSM-22 deactivation catalyst (FD-1, Carbon content is 7.24wt%), and the catalyst number after 2 hours of distillation is Ea-1.
[0033] Take 100g of Ca-1 catalyst, add 15g of nickel nitrate (nickel content 3.0wt%) solution for impregnation, and prepare a nickel-containing sample with an atomic ratio of Ni to Pt of 3:1, and then heat up at a rate of 3°C / min. The temperature was kept at 250°C for 10 hours, and then the temperature was raised to 410°C for 3 hours at a rate of 3°C / min to obtain the catalyst E-1 of the present invention.
Embodiment 2
[0035] The preparation of catalyst E-2 of the present invention
[0036] Take 100g of Ea-1 catalyst, add 10g of nickel acetate (8.0wt% nickel content) solution for impregnation to prepare a nickel-containing sample, wherein the atomic ratio of Ni to Pt is 5:1, and then the temperature is increased at a rate of 3°C / min , heated to 240°C for 10 hours, and then continued to heat up to 420°C for 3 hours at a rate of 3°C / min. The obtained catalyst was numbered Eb-1. Its physical and chemical properties are shown in Table 2, and the results are shown in Table 3
Embodiment 3
[0038] The preparation of catalyst E-3 of the present invention
[0039] Add 1450ml of organic solvent (the volume ratio of gasoline and kerosene is 1:1) into a 2000ml flask to treat the deactivated catalyst FD-1 after industrial operation, and the catalyst number after 2 hours of distillation is Cb-1.
[0040] Take 120g of Cb-1 catalyst, add 50g of nickel sulfate (Ni content 2.0wt%) solution for impregnation to prepare a nickel-containing sample, wherein the atomic ratio of Ni to Pt is 6:1, and then increase the temperature at a rate of 3°C / min , heated to 280° C. for 8 hours, and then continued to heat up to 350° C. for 5 hours at a rate of 3° C. / min to obtain the catalyst E-3 of the present invention. Its physical and chemical properties are shown in Table 3, and the reaction results are shown in Table 4.
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