Catalyst for dewaxing lubricating oil base oil produced by Fischer-Tropsch synthetic wax and preparation method and application of catalyst
A technology for lubricating base oil and Fischer-Tropsch synthetic wax, which is applied in the direction of molecular sieve catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems such as unsatisfactory turbidity reduction effect and blank catalyst for lubricating base oil dewaxing
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[0051] According to the method for preparing catalyst of the present invention, preferably, in step (1), the process of said surface passivation-shrinkage cavity treatment comprises:
[0052] (a) mixing the passivation-shrinkage agent with a solvent to prepare the first solution;
[0053] (b) contacting the acidic molecular sieve with the first solution at 20-90°C, followed by the first drying and the first calcination;
[0054] Preferably, the conditions for the first drying include: the temperature is 40-120°C, and the time is 1-12h;
[0055] The conditions for the first calcination include: the temperature is 200-600°C, and the time is 1-12h.
[0056] As long as the purpose of dissolving the passivation-shrinker agent can be achieved, the solvent can be selected from solvents known in the art. Preferably, the solvent is selected from water, methanol, ethanol, low-carbon (carbon number≤10) alkanes, such as butane, n-pentane, isopentane, n-heptane, n-hexane, etc.
[0057] ...
Embodiment 1
[0093](1) Mix 1.78g tetraethyl orthosilicate and 100mL n-hexane evenly, add 20g H-type SAPO-11 molecular sieve (average pore size is 0.6nm) to the obtained solution, stir at 70°C for 6h, then heat up to 90°C and evaporate Dry solvent. The obtained powder was dried in an oven at 120° C. for 4 hours, and then transferred to a muffle furnace for calcination at 550° C. for 4 hours to obtain a modified molecular sieve with an average pore size of 0.5 nm.
[0094] (2) Evenly mix the modified molecular sieve with 40g of alumina and 1.2g of scallop powder, then add a solution consisting of 1.8g of nitric acid and 42g of deionized water, knead in a kneader and extrude into a clover in an extruder Type, the strip obtained was dried at 120°C for 8h and calcined at 500°C for 6h to obtain the carrier.
[0095] (3) Dissolve 0.95g of chloroplatinic acid completely in 36mL of deionized water, add the obtained solution to the carrier described in step (2), then dry in an oven at 120°C for 12h...
Embodiment 2
[0097] (1) Mix 1.5g methyl silicone oil and 100mL n-heptane evenly, add 20g H-type mercerized molecular sieve (average pore size: 0.7nm) to the resulting solution, stir at 50°C for 8h, then heat up to 90°C and evaporate the solvent to dryness. The obtained powder was dried in an oven at 120 °C for 4 h, and then transferred to a muffle furnace for calcination at 550 °C for 4 h. Repeat the above steps once to obtain a modified molecular sieve with an average pore size of 0.4 nm.
[0098] (2) The modified molecular sieve is uniformly mixed with 30g aluminum oxide and 1g scallop powder, then added a solution composed of 2g nitric acid and 35g deionized water, kneaded in a kneader and extruded into a bar shape in an extruder, The strip obtained was dried at 120° C. for 8 hours, and calcined at 500° C. for 6 hours to obtain a carrier.
[0099] (3) Dissolve 0.44g tetraammineplatinum dichloride completely in 30mL deionized water, drop the obtained solution into the carrier described ...
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