Preparation method for hydrodewaxing catalyst and catalyst prepared by using same, and application of catalyst
A hydrodewaxing and catalyst technology, which is applied in molecular sieve catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of complex process start-up process, and achieve the effect of high yield and high isomerization selectivity.
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[0028] The invention provides a method for preparing a hydrodewaxing catalyst, the method comprising: a. first impregnating a molecular sieve-inorganic oxide carrier with a solution containing a hydrogenation active metal salt, followed by drying, roasting and reduction in sequence to obtain Supported catalyst; wherein, the molecular sieve is a molecular sieve with a one-dimensional elliptical pore structure, and the minor axis of the one-dimensional elliptical pore structure is The major axis of the one-dimensional elliptical hole structure is b. The supported catalyst obtained in step a is impregnated with water for the second time and dried to obtain a hydrodewaxing catalyst; wherein, the weight loss of the hydrodewaxing catalyst after roasting at 450°C for 4 hours is 0.2-5.0% by weight, preferably 0.5-2.0% by weight.
[0029] According to the method of the present invention, the weight loss refers to the ratio of the loss of catalyst weight before and after calcination ...
specific Embodiment approach
[0032] According to a specific embodiment of the method of the present invention, the preparation method of the molecular sieve-inorganic oxide carrier may be: mixing the molecular sieve with the matrix, extruding, drying and calcining. When forming by extrusion molding, an appropriate amount of extrusion aid and / or adhesive can be added, and then extruded. The type and amount of the extrusion aid and peptizer are well known to those skilled in the art, and will not be repeated here. The drying temperature is preferably 100-200°C, more preferably 120-150°C, and the drying time is preferably 1-20 hours, more preferably 2-10 hours. The calcination temperature is preferably 400-650°C, more preferably 500-600°C, and the calcination time is preferably 1-15 hours, more preferably 2-10 hours.
[0033] According to the method of the present invention, the hydrogenation active metal salt can be a soluble hydrogenation active metal salt commonly used in the art, for example, it can be ...
Embodiment 1
[0047] Describe the catalyst provided by the invention and its preparation method.
[0048] After mixing the organic template, the silicon source and the aluminum source, the crystallization was carried out in a stainless steel reaction kettle at 400 Rpm at 160° C. for 96 hours to obtain 100% ZSM-22 molecular sieve. Among them, the organic template is ethyl pyridinium bromide, and the aluminum source is Al 2 (SO4) 3 ·16H 2 O, the silicon source is silica sol (SiO 2 Content is 30% by weight), the SiO of feeding 2 / Al 2 o 3 60, H 2 O / SiO 2 40,OH - / SiO 2 0.3, K + / SiO 2 is 0.43, template / SiO 2 The silicon-aluminum molar ratio of ZSM-22 molecular sieve is 67. Gained molecular sieve 100 grams to contain 20% by weight NH 4 NO 3 1000 ml of the solution was treated at 80° C. for 4 hours, filtered, and treated 3 times in total by the above method. The treated molecular sieves were dried at 120° C. for 4 hours. The hydrogen ZSM-22 molecular sieve was obtained.
[0049...
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