Hydrogenation active protective agent with ivb group metal-containing alumina as carrier, preparation and application
A hydrogenation activity protection, alumina carrier technology, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve downstream catalyst deactivation and other problems
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Embodiment 1
[0035] Example 1 illustrates the macroporous alumina carrier used in the catalyst provided by the present invention and its preparation method.
[0036] Example 1
[0037] Take by weighing the dry rubber powder (dry basis is 73% that Changling Refinery Catalyst Factory produces, and wherein pseudo-boehmite content is 68%, and gibbsite content is 5 weight %, and surplus is amorphous alumina) 1000 gram, 36 grams of fennel powder (product of Henan Lankao Tianjing Rubber Factory), 25g hydroxymethyl cellulose are mixed homogeneously. Take 12g of titanium tetrachloride and dissolve it with 1000mL deionized water to form a salt solution; take 20mL of nitric acid and add 200mL of deionized water to prepare a dilute acid solution; Aluminum stone powder, kneading for 20 minutes. Extrude into a butterfly bar with an outer diameter of φ1.1mm on a twin-screw extruder. The wet strip was dried at 120°C for 4 hours and calcined at 880°C for 4 hours to obtain carrier Z1. The physical and c...
Embodiment 2
[0042] Get the carrier Z1200 grams that embodiment 1 prepares, use 500 milliliters to contain V 2 o 5 50 g / L, NiO14 g / L mixed solution of ammonium metavanadate and nickel nitrate was impregnated for 1 hour, filtered, dried at 120°C for 4 hours, and calcined at 400°C for 3 hours to obtain protective agent C1. The composition of protective agent C1 is listed in Table 2.
Embodiment 3
[0046] Get the carrier Z1200 grams that embodiment 1 prepares, use 500 milliliters to contain V 2 o 5 18 g / L, NiO 29 g / L mixed solution of ammonium metavanadate and nickel nitrate was impregnated for 1 hour, filtered, dried at 120°C for 4 hours, and calcined at 400°C for 3 hours to obtain protective agent C2. The composition of protectant C2 is listed in Table 2.
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