Method for preparing sulfurization type hydro-cracking catalyst
A hydrocracking and catalyst technology, which is applied in the direction of physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of delayed start-up time, reduced catalyst hydrogenation activity, and high cost, so as to improve utilization efficiency and improve Hydrogenation performance, the effect of improving performance
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Embodiment 1
[0031] The catalyst catA involved in the present invention.
[0032] Prepare 500 ml of ammonium tetrathiomolybdate solution (a), the slurry contains 5g molybdenum / 100ml, prepares 40ml of nickel nitrate solution (b), contains 5g nickel / 100ml in the slurry, weighs 120g of amorphous silica-alumina dry rubber powder, 30gY molecular sieve powder (SiO 2 / Al 2 o 3 The molar ratio is 40, the unit cell constant is 2.432nm, the infrared acidity is 0.19mmol / g, and the specific surface area is 866m 2 / g, pore volume 0.52ml / g), added to 1500g water to make a slurry (c), 10g polyethylene glycol ether was dissolved in 100mL water to form a solution (d), (a) and (b) were slowly added to the slurry In (c), introduce solution (d) at the same time and stir evenly. Filter, wash, and dry the obtained material at 100° C. for 6 hours under the protection of an inert gas to obtain a catalyst intermediate. Put the catalyst intermediate into the rolling machine and mix evenly, then add 180g of adh...
Embodiment 2
[0034] Catalyst catB involved in the present invention
[0035] Prepare 200 ml of tetramethylammonium thiomolybdate slurry (a), the slurry contains 10g molybdenum / 100ml, prepare 15ml of nickel nitrate solution (b), the slurry contains 10g nickel / 100ml, weigh 110g of amorphous silica-alumina dry glue powder, 28gβ molecular sieve powder (SiO 2 / A1 2 o 3 =28 (molecular ratio), the unit cell constant is 1.198nm, the relative crystallinity is 95%, the infrared acidity is 0.174 mmol / g, and the specific surface area is 894m 2 / g, pore volume 0.541ml / g), was added to 1500g water to make a slurry (c), 8g polyoxyethylene amine was dissolved in 100mL water to form a solution (d), (a) and (b) were slowly added to the slurry ( c), introduce solution (d) at the same time, and stir evenly. Filter, wash, and dry the obtained material at 110° C. for 6 hours under the protection of an inert gas to obtain a catalyst intermediate. Put the catalyst intermediate into the rolling machine and mi...
Embodiment 3
[0037] Catalyst catC involved in the present invention
[0038] Prepare 500 ml of ammonium tetrathiotungstate solution (a), the slurry contains 5g tungsten / 100ml, prepare 40ml of nickel nitrate solution (b), the slurry contains 5g nickel / 100ml, weigh 120g of amorphous silica-alumina dry rubber powder, 30gY molecular sieve powder (SiO 2 / Al 2 o 3 The molar ratio is 40, the unit cell constant is 2.432nm, the infrared acidity is 0.19mmol / g, and the specific surface area is 866m 2 / g, pore volume 0.52ml / g), was added to 1500g water to make a slurry (c), 15g polyoxyethylene amide was dissolved in 100ml water to form a solution (d), (a) and (b) were slowly added to the slurry ( c), introduce solution (d) at the same time, and stir evenly. Filter, wash, and dry the obtained material at 100° C. for 6 hours under the protection of an inert gas to obtain a catalyst intermediate. Put the catalyst intermediate into the rolling machine and mix evenly, then add 180g of binder made by p...
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