Selective hydrogenation for preparing hexabydrobenzoic acid from benzoic acid
A technology of hexahydrobenzoic acid and benzoic acid, applied in the direction of ozone oxidation to prepare carboxylic acid, organic chemistry, etc., can solve the problem of less research
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example 1
[0024] Prepare the catalyst used in the present invention
[0025] (1) Preparation of carrier: Take 100 grams of CI hydrated alumina powder (manufactured by Condea, Germany), whose physical and chemical properties are shown in Table 1. Add 1.0 g of Squatia powder to the above-mentioned hydrated alumina powder and mix evenly, then add 50 ml of dilute nitric acid with a concentration of 3% by volume, stir and knead, then extrude into strips with an outer diameter of 1 mm, dry at 120°C for 2 hours, cut off Grow strips with a length of 2-3 mm, and bake at 850° C. for 4 hours to obtain carrier a, whose physical and chemical properties are shown in Table 2. The specific surface and pore volume in the physical and chemical properties are determined by low-temperature nitrogen adsorption BET method, and the number of acid centers is determined by NH 3 - Determination by TDP method (see "Zeolite Catalysis and Separation Technology", edited by Gao Zi et al., P19, China Petrochemical Pr...
example 2~5
[0034] This example is the benzoic acid selective hydrogenation activity experiment of catalyst.
[0035] Catalysts A, B, C, and D were evaluated for hydrogenation activity in a 20 ml fixed-bed reactor. Get 10 grams of catalyst and pack it into the reaction tube, raise the bed temperature to 180°C, pass hydrogen, the molar ratio of hydrogen to benzoic acid is 5:1, the reaction pressure is 1.0MPa, and the space velocity is 2 hours -1 ,use figure 1 The shown fixed bed reactor was used for trickle bed reaction, and the reaction results are shown in Table 4.
example 6
[0037] Catalyst A was placed in a 20 ml fixed-bed reaction device, and evaluation tests were carried out under different reaction conditions. The results are shown in Table 5.
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[0039] example
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[0042] Reaction conditions
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