Aromatic hydrocarbon hydrogenation catalyst and its preparation method
A technology for hydrogenation of aromatics and catalysts, applied in chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, etc., can solve the problem of low hydrogenation activity of aromatics and achieve high hydrogenation Effects of hydrogen reactivity, simplification of operation, and shortening of the production process
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Embodiment 1
[0021] Weigh 84.75g of basic nickel carbonate powder, add 1.0mol L -1 36.0mL of boric acid solution, then add 1.0mol·L -1 64.0mL of ammonium metatungstate solution, and mix the above materials evenly. Dry the mixed material at 100°C for 5 hours, and then roast the material at 350°C for 5 hours. The calcined material is pressed into tablets to obtain the catalyst, which consists of (based on the weight of the catalyst): NiO=75.6%, B 2 o 3 = 1.9%, WO 3 = 22.5%. Catalyst A has an average pore diameter of 5.30nm and a pore volume of 0.278ml·g -1 , the specific surface area is 242m 2 g -1 . Its composition and properties are shown in Table 1.
[0022] The activity evaluation experiment of catalyst hydrogenation reaction adopts flow type differential reactor-gas chromatography device as the activity evaluation device. The reaction raw material is containing 120mg·L -1 Carbon disulfide in ethylbenzene liquid. The catalyst was first reduced at 400°C for 3 hours under a hyd...
Embodiment 2
[0027] The preparation steps are as in Example 1. Weigh 84.75 g of basic nickel carbonate and add 1.0 mol L -1 144.0mL of boric acid solution, then add 1.0mol·L -1 107.0mL of ammonium metatungstate solution, mixed evenly, dried at 100°C for 5h, and then roasted at 450°C for 3h. The catalyst was obtained by tablet molding, and its composition and properties are shown in Table 1.
[0028] The activity evaluation of the catalyst is the same as in Example 1, and the results are shown in Table 2.
Embodiment 3
[0030] The preparation steps are as in Example 1. Weigh 84.75 g of basic nickel carbonate and add 1.0 mol L -1 108.0mL of boric acid solution, and then add 27.90g of ammonium paratungstate powder, mix well and bake at 450°C for 5h. Tablet 1 obtained Catalyst C, its composition and properties.
[0031] The activity evaluation of the catalyst is the same as in Example 1, and the results are shown in Table 2.
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