Dewaxing catalyst for lubricant oil distillate and its uses
A catalyst and lubricating oil technology, which is applied in the lubricating oil hydrodewaxing catalyst and its application in the lubricating oil hydrodewaxing process, and can solve the problems of easy cracking, lower liquid yield, matching of acid function and hydrogenation function Inappropriate and other issues
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[0019] Provide a kind of specific preparation method of catalyst of the present invention below, but not limited to this method, concrete steps are:
[0020] (1) Fully kneading molecular sieves, inorganic refractory oxides, extrusion aids, water and peptizers together to form a plastic paste, extruded into strips, dried and roasted to obtain a catalyst carrier;
[0021] (2) Using an aqueous solution containing an active metal component, selectively adding a water-soluble compound containing an auxiliary agent, drying and roasting to obtain the catalyst of the present invention;
[0022] Wherein zinc can be before step (2), impregnate the catalyst support that step (1) obtains with zinc-containing aqueous solution, through drying, roasting, obtain zinc-containing catalyst support; Also can impregnate on the catalyst support together with active metal component; Also The active metal can be dipped first, followed by zinc; one of the first two methods is preferred.
[0023] The ...
Embodiment 1
[0042] A kind of preparation method of catalyst of the present invention
[0043] Take 200 grams of S-1 carrier, use the 3 ) 4 Cl 2 Saturated impregnation with a solution of zinc acetate, then dried at 100°C for 8 hours, and calcined at 500°C for 3 hours in an air atmosphere to obtain a catalyst of the present invention containing 0.6wt% Pt and 2.4wt% Zn, numbered as E-1, which The physical and chemical properties are shown in Table 3, and the reaction results are shown in Table 4.
Embodiment 2
[0045] A kind of preparation method of catalyst of the present invention
[0046] Take 200 grams of S-2 carrier, use a solution containing palladium nitrate and zinc chloride to carry out ion exchange at 60°C for 12 hours, then dry at 110°C for 6 hours, and bake at 480°C for 4 hours in an air atmosphere to obtain 0.8wt The catalyst of the present invention with %Pd and 0.6wt% Zn is numbered E-2, its physicochemical properties are shown in Table 3, and the reaction results are shown in Table 4.
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