Preparation method of adsorbent for CO pressure swing adsorption
A pressure swing adsorption and adsorbent technology, which is applied in the chemical industry and can solve the problems of low mechanical strength and low adsorption efficiency.
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Embodiment 1
[0037] Weigh 1gX molecular sieve, add 17g of sodium aluminate solution with mass concentration of 40%, and 20g of tetrapropylammonium bromide solution with mass concentration of 6%, then crystallize at 120°C for 5h, cool, wash and dry. The first modified carrier.
[0038] Afterwards, the first modified carrier is placed in water so that the mass ratio of the first modified carrier to water is 3:7, and then ethylenediamine is added so that the mass ratio of water to ethylenediamine is 5:1. Then, it was treated in gas-solid phase at 160° C. for 15 hours, washed with water and dried to obtain a second modified carrier.
[0039] Weigh 10 g of the second modified carrier, mix it with 3 g of cuprous chloride and an appropriate amount of water, mix it evenly, extrude it, leave it to stand and then dry it to obtain an adsorbent precursor.
[0040] The obtained adsorbent precursor was placed in a muffle furnace, calcined at 200°C for 5 hours, then soaked in a 5% hydrochloric acid solu...
Embodiment 2
[0043] Weigh 1g SAPO-34 molecular sieve, add 25g mass concentration of 40% aluminum sulfate solution, 15g mass concentration of 5% n-propylamine solution and 12g mass concentration of 5% phosphoric acid solution, then crystallize at 110 ° C for 4h, after cooling, washing with water and drying to obtain the first modified carrier.
[0044]Afterwards, the first modified carrier was placed in water so that the mass ratio of the first modified carrier to water was 3:7, and then n-butylamine was added to make the mass ratio of water to ethylenediamine 6:1. Then, it was treated in gas-solid phase at 150° C. for 12 hours, washed with water and dried to obtain a second modified carrier.
[0045] Weigh 10 g of the second modified carrier, mix it with 3 g of cuprous chloride and an appropriate amount of water, mix it evenly, extrude it, leave it to stand and then dry it to obtain an adsorbent precursor.
[0046] The prepared adsorbent precursor was placed in a muffle furnace, calcined ...
Embodiment 3
[0049] Adsorbent C was prepared in the same manner as in Example 1, except that aluminum acetate was used instead of sodium aluminate in Example 1.
[0050] The mechanical strength of the adsorbent C and the carbon monoxide adsorption capacity at 18° C. and a carbon monoxide pressure of 760 mmHg were tested, and the results are shown in Table 1.
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