Preparation method of sulfuration 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 problems such as delayed start-up time, toxicity, and low metal utilization rate, so as to improve hydrogenation performance and avoid Effect of low solubility and improved utilization efficiency
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Embodiment 1
[0030] The present invention relates to a catalyst catA.
[0031] Prepare 250 ml of ammonium heptamolybdate solution (a), 100ml of 10g molybdenum in the solution, 500ml of 10wt% ammonium sulfide solution (b), prepare 40ml of nickel nitrate solution (c), the slurry contains 5g nickel / 100ml, weigh 120g Amorphous silica-alumina dry rubber powder, 30gY molecular sieve powder (SiO 2 / Al 2 O 3 Molar ratio is 40, unit cell constant is 2.432nm, infrared acidity is 0.19mmol / g, specific surface area is 866m 2 / g, pore volume 0.52ml / g), add to 1500g water to make a slurry (d), slowly add (a), (b) and (c) to the slurry (d), stir evenly, and control the system temperature to 65℃ After reacting for 1 hour, it is filtered, washed, and the obtained material is dried at 100°C for 6 hours under the protection of inert gas to obtain a catalyst intermediate. After the catalyst intermediate is put into a roller compactor and mixed uniformly, 180g of a binder made by peptizing nitric acid and SB alumi...
Embodiment 2
[0033] The present invention relates to the catalyst catB.
[0034] Prepare 400 ml ammonium tetramolybdate solution (a), the solution contains 5g molybdenum 100 / ml, prepare 15wt% ammonium sulfide solution 300ml (b), prepare 30ml nickel nitrate solution (c), the slurry contains 8 nickel / 100ml, weigh Take 110g amorphous silicon-aluminum dry rubber powder, 28g β molecular sieve powder (SiO 2 / A1 2 O 3 =28 (molecular ratio), unit cell constant is 1.198nm, relative crystallinity is 95%, infrared acidity is 0.174mmol / g, specific surface area is 894m 2 / g, pore volume 0.54lml / g), add to 1500g of water to make a slurry (d), slowly add (a), (b) and (c) to the slurry (d), stir evenly, and control the system temperature to 65℃ After reacting for 1 hour, filter, wash, and dry the obtained material at 110°C for 5 hours under the protection of inert gas to obtain a catalyst intermediate. After the catalyst intermediate is put into a roller compactor and mixed uniformly, 180g of a binder made b...
Embodiment 3
[0036] The present invention relates to the catalyst catC.
[0037] Prepare 250 ml of ammonium metatungstate solution (a), 100ml of 10g tungsten in the solution, 500ml of 10wt% ammonium sulfide solution (b), prepare 40ml of nickel nitrate solution (c), the slurry contains 5g nickel / 100ml, weigh 120g Amorphous silica-alumina dry rubber powder, 30gY molecular sieve powder (SiO 2 / Al 2 O 3 Molar ratio is 40, unit cell constant is 2.432nm, infrared acidity is 0.19mmol / g, specific surface area is 866m 2 / g, pore volume 0.52ml / g), add to 1500g water to make a slurry (d), slowly add (a), (b) and (c) to the slurry (d), stir evenly, and control the system temperature at 60℃ After reacting for 1 hour, filter, wash, and dry the obtained material at 100°C for 6 hours under the protection of inert gas to obtain a catalyst intermediate. After the catalyst intermediate is put into a roller compactor and mixed uniformly, 180g of a binder made by peptizing nitric acid and SB alumina is added, kne...
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