Clean preparation method of hydrogenation catalyst carrier
A technology for hydrogenation catalysts and catalyst carriers, which is applied in the direction of catalyst carriers, chemical instruments and methods, physical/chemical process catalysts, etc., and can solve problems such as catalyst fracture, fragmentation, and destruction, and achieve the effects of easy operation and simple preparation methods
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preparation example Construction
[0026] The preparation process of the catalyst carrier of the present invention includes: mixing the modified catalyst carrier components, such as macroporous alumina powder and / or amorphous silica-alumina dry rubber powder, and other extrusion aids, such as pore expanders, lubricants, etc. After fully dry mixing, add organic acid binder to form and extrude, and the orifice plate of the extruder can be cylindrical, clover, four-leaf clover or other special shapes, and then low-temperature drying, microwave treatment, high-temperature roasting activation, prepared. Hydrotreating catalyst supports.
[0027] The preparation process of the catalyst carrier of the present invention will be specifically described below.
[0028] 1) To prepare an organic acid solution, weigh 1320g of oxalic acid (oxalic acid) white crystals, dissolve it in distilled water with constant temperature stirring at 50°C, and stir for 20 minutes to prepare a transparent 5000mL organic acid solution with a p...
example 1
[0035] Example 1 (Comparative Scheme)
[0036] Take 1280mL of dilute nitric acid solution (concentration is 4g nitric acid / 100mL), gradually add 720g of small-hole pseudo-boehmite (SB powder produced in Germany), after standing for 20 minutes, stir evenly to form a white translucent paste, stand still at room temperature After 8h, the adhesive was prepared. Take 580g of macroporous alumina (produced by Tianjin Chenoa Company, pore volume 0.80mL / g, specific surface area 295m 2 / g, 72.1% on a dry basis), add 6g of saffron powder, add 562.9g of binder, roll for 30 minutes, add an appropriate amount of distilled water to make the mixture into a paste that can be squeezed, extrude, extruder orifice plate 1.5mm diameter clover. The wet bar was dried at 120°C for 4 hours, then calcined at 550°C for 3 hours, code HT-1S.
example 2
[0037] Example 2 (Comparative Scheme)
[0038] The dilute nitric acid solution of Example 1 was replaced with an acetic acid solution (concentration: 13.2 g acetic acid / 100 mL), and the others were the same as in Example 1, and a carrier was prepared, numbered HT-2S.
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