Method for producing lubricating oil base oil
A technology for lubricating base oil and production method, which is applied in the petroleum industry, processing hydrocarbon oil, etc., can solve problems such as poor pour point depressant effect and low yield, and achieve the effect of improving yield and pour point depressant effect.
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example 1
[0025] This example illustrates the catalyst I used in the method provided by the invention and its preparation method.
[0026]The ZSM-22 molecular sieve used in this example was synthesized according to the patent U.S. Pat. No. 4,556,477 method. Weigh 286 grams of silica sol (silica content 25% by weight), and add 298 grams of distilled water to obtain a silica sol solution. Take by weighing 10 grams of aluminum sulfate (product of Beijing Chemical Plant, analytically pure, aluminum oxide content 15.3 weight %), be dissolved in 260 grams of distilled water; Take by weighing 23 grams of potassium hydroxide (product of Beijing Chemical Plant, analytically pure), be dissolved in 263 grams of distilled water. Under vigorous stirring, the aluminum sulfate solution was slowly added dropwise to the potassium hydroxide solution, and then the silica sol solution was added dropwise to the solution, and the stirring was continued for 15 minutes. Under vigorous stirring, 50 grams of 1...
example 2
[0030] This example illustrates the catalyst I used in the method provided by the invention and its preparation method.
[0031] The ZSM-22 molecular sieve synthesized in 173.3 gram alumina powders (same example 1) and 70 gram example 1 is mixed homogeneously, extruded into the trilobal bar that circumscribed circle diameter is 1.4 millimeters, dried 4 hours in 120 ℃ of air, 560 ℃ under an air atmosphere for 4 hours to prepare the catalyst carrier Z2.
[0032] Take 100 grams of carrier Z2, impregnate it with 80 milliliters of tetraammine platinum dichloride solution containing 0.3 grams of platinum for 4 hours, dry it in air at 120° C. for 4 hours, and roast it in a tube furnace at 450° C. for 4 hours to obtain catalyst C2. The composition of catalyst C2 is listed in Table 1.
example 3
[0034] This example illustrates the catalyst II used in the method provided by the invention and its preparation method.
[0035] The SAPO-11 molecular sieve used in this example was synthesized according to the method of Example 16 in the patent U.S. Pat. No. 4,440,871. Weigh 420 grams of 85% by weight phosphoric acid, add 880 grams of distilled water, 276 grams of pseudoboehmite (alumina content of 74.2% by weight, water content of 25.8% by weight), and stir evenly to obtain a mixture S1. Weigh 1298.4 grams of 40% by weight aqueous solution of hydroxytetra-n-butylamine and 52 grams of fumed silica gel (92.8% by weight of silicon oxide, 7.2% by weight of water), and stir evenly to obtain a mixture S2. The mixtures S1 and S2 were mixed, and 204 g of di-n-propylamine were added with stirring to obtain a reaction mixture. The reaction mixture was packed into a polytetrafluoroethylene-sealed reaction kettle, crystallized at 200°C for 24 hours, filtered, washed to neutrality, and...
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