A clean preparation method for 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. It can solve the problems of catalyst breakage, fragmentation, and inability to meet preparation requirements, and achieves simple and easy preparation methods. The effect of the operation
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preparation example Construction
[0026] The preparation process of the catalyst carrier of the present invention comprises: modifying the catalyst carrier components such as macroporous alumina powder and / or amorphous silica-alumina colloidal powder, and other extrusion aids, such as pore-enlarging agents, lubricants, etc. After fully dry mixing, add organic acid binder to shape and extrude. The orifice of the extruder can be cylindrical, clover, four-leaf clover or other special shapes, and then dry at low temperature, microwave treatment, and high-temperature roasting to activate. Hydrotreating catalyst support.
[0027] The preparation process of the catalyst carrier of the present invention will be described in detail below.
[0028] 1) Prepare an organic acid solution, weigh 1320g of oxalic acid (oxalic acid) white crystals, dissolve it in distilled water stirred at a constant temperature of 50°C, and stir for 20 minutes to prepare a transparent 5000mL organic acid solution with a pH value of about 0.9. ...
example 1
[0035] Example 1 (comparison scheme)
[0036] Take 1280mL dilute nitric acid solution (concentration: 4g nitric acid / 100mL), gradually add 720g small-pore pseudo-boehmite (SB powder produced in Germany), after standing still for 20min, 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 Chenoya Company, with a pore volume of 0.80mL / g and a specific surface area of 295m 2 / g, dry basis 72.1%), add 6g of scallop powder, and 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 extruded, extruded, extruded machine orifice 1.5mm clover in diameter. The wet strips were dried at 120°C for 4 hours, and then calcined at 550°C for 3 hours, numbered HT-1S.
example 2
[0037] Example 2 (comparison scheme)
[0038] The dilute nitric acid solution in Example 1 was replaced with acetic acid solution (concentration: 13.2g acetic acid / 100mL), and the others were the same as in Example 1 to prepare a carrier, numbered HT-2S.
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