Startup method of sulfuration type hydrogenation catalyst
A hydrogenation catalyst and a sulfurized type technology are applied in the field of the start-up of sulfurized hydrogenation catalysts, which can solve the problems of loss of active components and decrease in catalyst activity, and achieve the effects of saving start-up time, improving hydrogenation activity and being environmentally friendly.
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Embodiment 1
[0034] The preparation of embodiment 1 catalyst A
[0035] Get 100g oxidation state catalyst I, pass into the mixed gas of hydrogen and hydrogen sulfide, H 2 :H 2 S=4:1, heat up to 300°C for 6 hours of vulcanization, cool down and take out the catalyst to obtain a vulcanized catalyst. Spray and immerse with an aqueous solution of nickel citrate (2.5g / 100ml in terms of nickel), so that the introduced nickel citrate (in terms of nickel oxide) accounts for 0.5% of the weight of the sulfurized catalyst, and then treat it at 150°C under nitrogen protection After 6 hours, catalyst A was obtained.
[0036] Put catalyst A into the reactor, keep the nitrogen pressure at 3.4MPa, directly raise the temperature to 120°C, introduce straight-run diesel oil, continue to raise the temperature to 300°C, keep the temperature for 6 hours, then cool down to 280°C, replace the nitrogen with hydrogen, and replace the raw materials at the same time Oil, the hydrogenation reaction starts after 24 ho...
Embodiment 2
[0037] The preparation of embodiment 2 catalyst B
[0038] Take 100g of oxidation state catalyst II, pass through hydrogen, raise the temperature to 120°C and start to feed vulcanized oil, which contains CS 2 5% (v%), after constant temperature for 1 hour, continue to heat up to 230°C for 3 hours, then heat up to 320°C for 3 hours, cool down and take out the catalyst to obtain a vulcanized catalyst. Spray and immerse with an aqueous solution of cobalt citrate (concentration calculated as cobalt: 4.5g / 100ml), so that the introduced cobalt citrate (calculated as cobalt oxide) accounts for 1% of the weight of the sulfurized catalyst, and then treat it under air at 120°C for 12 hours, the catalyst B was obtained.
[0039] The start-up and reaction conditions are the same as in Example 1, and the hydrodesulfurization activity is shown in Table 2.
Embodiment 3
[0040] The preparation of embodiment 3 catalyst C
[0041] Get 100g oxidation state catalyst III, pass into the mixed gas of hydrogen and hydrogen sulfide, H 2 :H 2 S=4:1, heat up to 300°C for 6 hours of vulcanization, cool down and take out the catalyst to obtain a vulcanized catalyst. Spray and immerse with an aqueous solution of nickel citrate (2.5g / 100ml in terms of nickel), so that the introduced nickel citrate (in terms of nickel oxide) accounts for 0.5% of the weight of the sulfurized catalyst, and then treat it at 150°C under nitrogen protection After 6 hours, catalyst C was obtained.
[0042] Put catalyst C into the reactor, start the circulating compressor after the airtightness is qualified, raise the pressure to 4.0MPa with nitrogen, raise the temperature of the catalyst bed to 120°C, introduce coked kerosene (nitrogen content is 0.035wt%), and continue to raise the temperature to 300°C, keep the temperature constant for 6 hours, then cool down to 280°C, replace...
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