Iron-based catalyst with high carbon hydrocarbon selectivity as well as preparation method and application thereof
An iron-based catalyst, a selective technology, applied in catalyst activation/preparation, carbon compound catalysts, catalysts, etc., to achieve the effect of simplifying the preparation process and reducing the cost of catalysts
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Embodiment 1
[0033] (1) First, 34.75 grams of ferric sulfate is placed in a beaker, add 69.5 grams of deionized water, stirred with a magnet for 5 minutes to obtain a ferrous sulfate solution, add 15.75 grams of oxalic acid to the inside, and add 1.41 grams. Sodium tartrate, yellow turbid fluid, fully stirred to dispersed mixed; place the cloudy fluid in the centrifugal cup, centrifuged under 4000 rpm, 5 minute conditions, washed with 75 ml of deionized water, then centrifuged Separated, followed by pressing the supernatant twice; transferring the yellow precipitate after washing into the beaker, dried in an oven at 90 ° C for 12 hours, and fired at 500 ° C for 10 hours to give a brick powder, The powder tablets are formed into particles, which is recorded as a catalyst 1;
[0034] (2) Test of catalyst reaction performance: 1 gram catalyst 1 for fixing bed reactor evaluation, reduction temperature at 300 ° C, CO / N 2After 6 hours at atmospheric pressure reducing = 3, at 235 ℃, 1.6MPa, H 2 / C...
Embodiment 2
[0036] (1) first weighing 34.75 grams of ferrous sulfate placed in a beaker was added 52.5 g of deionized water, stirred with a magnetic ferrous sulfate solution was obtained after 5 minutes, 12.5 g of oxalic acid was added to the inside, while adding 2.82 g of sodium potassium tartrate, generating yellow turbid solution was sufficiently stirred until dispersed uniformly mixed; the turbid solution placed in a centrifuge cup and centrifuged at 4000 rpm / min for 5 minutes conditions, the precipitate was washed with 75 ml of deionized water, centrifuged again separation, the supernatant was removed after the above-described operation is repeated twice; yellow precipitate after washing was transferred to a beaker placed in a dry oven at 110 deg.] C for 10 hours, and calcined 600 ℃ 9 hours, to give brick-red powder, the pressed powder molded into particles, referred to as the catalyst 2;
[0037] (2) a reaction catalyst performance test: 1 g of catalyst 2 was evaluated in a fixed bed ...
Embodiment 3
[0039] (1) first weighing 34.75 grams of ferrous sulfate placed in a beaker was added 97.3 g of deionized water, stirred with a magnetic ferrous sulfate solution was obtained after 5 minutes, 22.58 grams of oxalic acid was added to the inside, while adding 8.47 g of sodium potassium tartrate, generating yellow turbid solution was sufficiently stirred until dispersed uniformly mixed; the turbid solution placed in a centrifuge cup and centrifuged at 4000 rpm / min for 5 minutes conditions, the precipitate was washed with 75 ml of deionized water, centrifuged again separation, the supernatant was removed after the above-described operation is repeated twice; yellow precipitate after washing was transferred to a beaker placed in a dry oven at 120 deg.] C for 12 hours, and calcined 650 ℃ 6 hours, to give brick-red powder, the pressed powder molded into pellets, as catalyst 3;
[0040] (2) a reaction catalyst performance test: 1 g of catalyst 3 used in evaluation of a fixed bed reactor,...
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