Preparation method of sulfurization type hydro-cracking catalyst
A hydrocracking and catalyst technology, applied in the direction of physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of low metal utilization, toxicity, and delayed start-up time, so as to achieve flexible active metal content and avoid Effect of low solubility and improved hydrogenation performance
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Embodiment 1
[0030] The catalyst catA involved in the present invention.
[0031] Prepare 500 ml of ammonium tetrathiomolybdate slurry (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), was added into 1500g water to make a slurry (c), slowly added (a) and (b) into the slurry (c), and stirred 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 adhesive made by peptizing nitric acid and SB alumina, knead, and roll to make a paste that can be extruded, and extruded into...
Embodiment 2
[0033] The catalyst catB involved in the present invention.
[0034] 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 (molar ratio), the unit cell constant is 1.198nm,
[0035] The relative crystallinity is 95%, the infrared acidity is 0.174mmol / g, and the specific surface area is 894m 2 / g, pore volume 0.54ml / g), was added into 1500g water to make a slurry (c), slowly added (a) and (b) into the slurry (c), and stirred 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 mix evenly, then add 180g of adhesive made by peptizing nitric acid and SB alumina, knead, and roll to make a pa...
Embodiment 3
[0037] The catalyst catC involved in the present invention.
[0038] Prepare 500 ml of ammonium tetrathiotungstate slurry (a), the slurry contains 5g tungsten 100ml, prepare nickel nitrate solution 40ml (b), the slurry contains 5g nickel / 100ml, weigh 120g amorphous silica aluminum 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 into 1500g water to make a slurry (c), slowly added (a) and (b) into the slurry (c), and stirred 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 adhesive made by peptizing nitric acid and SB alumina, knead, and roll to make a paste that can be extruded, and extruded into strips . ...
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