Hydrogenation catalysts precuring method and start working method of hydrogenation process
A catalyst and presulfurization technology, which is applied in the direction of catalyst activation/preparation, chemical instruments and methods, and start-up of hydroprocessing operations, etc., can solve the problems that affect the start-up of hydrogenation units on time, increase processing costs, and take a long time to achieve The effect of reducing human body damage, uniform pre-vulcanization process, and high sulfur efficiency
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Embodiment 1
[0040] 50 g of the catalyst 100 g is impregnated in 10 g of organic solvent (organic solvent is coking kerosene fraction), the ratio of carbon number 9 to 12 in the organic solvent is not less than 50%, and the immersion time is 1 hour. Elemental sulfur 10g and 5g (NH 4 ) 2 S mixed. The impregnated catalyst was mixed with a vulcanizing agent, treated at 180° C. for 3 hours, and cooled naturally to obtain a pre-sulfided catalyst A. Mix the obtained presulfurized catalyst A with the remaining 50g of the unpresulfurized catalyst evenly, put it into a small reactor, and make it airtight, adjust the hydrogen partial pressure to 6.0MPa and start to raise the temperature at 20°C / h, and start to rise to 80°C Add vulcanized oil, and carry out closed-circuit circulation of the device. The vulcanized oil is straight-run kerosene, and the condition is that the volume ratio of hydrogen to oil is 350:1, and the volume space velocity is 2.0h -1 . When the temperature rises to 270°C, keep...
Embodiment 2
[0042] 70 g of the catalyst 100 g was immersed in 10 g of organic solvent (the organic solvent was a mixture of coker kerosene fraction and cottonseed oil at a volume ratio of 2:1), and the soaking time was 1 hour. Elemental sulfur 10g and 5g (NH 4 ) 2 S mixed. The impregnated catalyst was mixed with a vulcanizing agent, treated at 150° C. for 5 hours, and cooled naturally to obtain a pre-sulfided catalyst A. The obtained vulcanizing agent A and the remaining non-presulfurized catalyst are respectively loaded into a small reactor, and the presulfurized catalyst is loaded on the top of the remaining oxidation state catalyst. The airtightness is qualified, the hydrogen partial pressure is adjusted to 6.0MPa, and the temperature is raised at 20°C / h. When it rises to 80°C, the vulcanized oil is added, and the device is closed-circuited. The vulcanized oil is straight-run kerosene, and the condition is that the volume ratio of hydrogen to oil is 350:1. Volumetric space velocity ...
Embodiment 3
[0044] 30 g of the catalyst 100 g was immersed in 10 g of organic solvent (the organic solvent was a fraction of coked diesel oil), and the immersion time was 1 hour. Elemental sulfur 12g and 5g (NH 4 ) 2 S mixed. The impregnated catalyst was mixed with a vulcanizing agent, treated at 200° C. for 2 hours, and cooled naturally to obtain a pre-sulfided catalyst A. The obtained presulfided catalyst A and the oxidation state catalyst without presulfurization treatment are loaded into small reactors respectively, and the loading is to load the presulfided catalyst on the top of the oxidation state catalyst. The airtightness is qualified, the hydrogen partial pressure is adjusted to 6.0MPa, and the temperature is raised at 20°C / h. When it rises to 80°C, the vulcanized oil is added, and the device is closed-circuited. The vulcanized oil is straight-run kerosene, and the condition is that the volume ratio of hydrogen to oil is 350:1. Volumetric space velocity 2.0h -1 . When the t...
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