Dehydrogenation catalyst, preparation method and application thereof, and method for preparing cyclohexanone by cyclohexanol dehydrogenation
A dehydrogenation catalyst and cyclohexanol technology are applied in the field of cyclohexanol dehydrogenation to prepare cyclohexanone, and can solve the problems of long time, low dehydrogenation temperature, unfavorable industrial application and the like
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0015] The invention provides a method for preparing a dehydrogenation catalyst, the method comprising: under co-precipitation conditions, contacting the soluble salt of the dehydrogenation active component with a precipitating agent capable of precipitating the cation of the soluble salt in water and then filtering to obtain Solid precipitate, dry or not dry the solid precipitate and roast; wherein, the dehydrogenation active component contains Zn element, Ca element and Ba element, and the molar ratio of Zn element, Ca element and Ba element 3-1000:5-50:1, and the contacting is carried out in the presence of an organic compound containing a functional hydroxyl group.
[0016] According to the preparation method of the dehydrogenation catalyst of the present invention, as long as the molar ratio of Zn element, Ca element and Ba element in the dehydrogenation active component is guaranteed to be 3-1000: 5-50: 1, and the contact is carried out in the The purpose of the present ...
preparation Embodiment 1
[0035] Configuration 2L concentration is the mixed aqueous solution of barium nitrate, calcium nitrate and zinc nitrate (wherein the molar ratio of zinc element: calcium element: barium element is 5: 20: 1) that concentration is 30% by weight;
[0036] Add 6g of monoethanolamine to the aforementioned mixed aqueous solution to obtain a mixed aqueous solution containing alcoholamine;
[0037] At 70°C, the aforementioned mixed aqueous solution containing alkanolamine was contacted with an aqueous sodium carbonate solution with a concentration of 2 mol / L for 2 hours, wherein the amount of sodium carbonate was controlled so that barium ions, calcium ions and zinc ions were all precipitated, and then the precipitated The material was filtered off and washed (washing until no nitrate was detected, using FeSO 4 solution and concentrated sulfuric acid test, which is called the nitrate ring test), and then baked at 610°C for 5 hours to obtain C1.
preparation Embodiment 2-8
[0039] Prepare the dehydrogenation catalyst C2-C8 according to the method for Preparation Example 1, the difference is that in the preparation process, the temperature of active components, co-precipitation and roasting temperature etc. change to some extent (see Table 1 for details, wherein it is the same as that of Preparation Example 1 The same conditions are not listed again).
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 