Regeneration and reactivation method for carbon deposition inactivation catalyst
A technology for deactivating catalysts and catalysts, which is used in catalyst regeneration/reactivation, catalyst activation/preparation, chemical instruments and methods, etc.
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Embodiment 1
[0022] Take a deactivated type II active phase hydrotreating catalyst with a carbon deposit of 4.9% and a sulfur content of 10.1%, and perform charcoal regeneration under different conditions in an oxygen-containing atmosphere.
[0023] Condition 1: Take 500mL deactivated catalyst, raise the temperature to 550°C at a heating rate of 3°C / min, and keep the temperature at 550°C for 3 hours. The obtained sample is named C1, and its carbon content is 0.05%.
[0024]Condition 2: Take 500mL deactivated catalyst, heat up to 230°C at a heating rate of 3°C / min, keep the temperature at 230°C for 10 hours, then continue to heat up to 350°C at a constant temperature of 3°C / min for 3 hours, and obtain The sample named C2 has a carbon content of 1.42%.
[0025] Condition 3: take 500mL deactivated catalyst, heat up to 300°C at a heating rate of 3°C / min, keep the temperature at 300°C for 6 hours, then continue to heat up at a heating rate of 3°C / min to 380°C for 5 hours, and obtain The sample...
Embodiment 2
[0027] Activate the regenerants C1 and C2 with ammonia water and citric acid. Take the mixed solution of ammonia water and citric acid and spray and immerse C1 and C2 in equal volumes. The molar ratio of NH3 and citric acid in the solution to the Ni atom on the regenerant is 2:0.8:1. After the sample is left for 4 hours, dry it at 120°C for 4 hours. The obtained catalysts were designated as C1-1 and C2-1, respectively.
Embodiment 3
[0029] Regenerant C2 is activated with ethanolamine and ethylene glycol. Take the mixed solution of ethanolamine and ethylene glycol and spray and immerse C2 in equal volume. The molar ratio of ethanolamine and ethylene glycol in the solution to the Ni atom on the regenerant is 0.8:1:1. After the sample is left for 4 hours, dry it at 120°C for 4 hours. The obtained catalysts were designated as C2-2, respectively.
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