Low-concentration methane separation adsorbent based on compounding of attapulgite nanorod crystal and two-dimensional metal organic framework and preparation method of low-concentration methane separation adsorbent
A technology of metal-organic framework and nanorod crystals, which is applied in separation methods, methane capture, and dispersed particle separation, etc., can solve the problems of no mention of methane/nitrogen separation ratio, no advantages, complex composition, etc., and achieve efficient selection Excellent adsorption capacity, low cost, and low adsorption opening pressure
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Embodiment 1
[0049] (1) Attapulgite nanorod crystals with a high aspect ratio greater than 20 and the silane coupling agent hydrolyzate are refluxed for 2 hours at a mass volume ratio of 50:1 g / ml; filtered, washed with distilled water until neutral;
[0050] (2) 1g of 4,4'-bipyridyl was dissolved in 100ml of ethanol to obtain solution A;
[0051] (3) 5g 2,5-dihydroxybenzoic acid and 0.8g copper nitrate trihydrate were dissolved in 100ml water to obtain solution B;
[0052] (4) Add 0.2g of neutral attapulgite nanorod crystals prepared in step (1) into solution A, then slowly add solution B, and mix evenly with ultrasonic waves;
[0053] (5) Put the mixed solution obtained in step (4) into an autoclave, let stand at 180° C. for 24 hours, and filter to obtain green needle-shaped crystals;
[0054] (6) Heat the green needle-shaped crystals to 110° C., and vacuum-dry for 5 hours to prepare the finished adsorbent.
Embodiment 2
[0056] (1) Attapulgite nanorod crystals with a high aspect ratio greater than 20 and a silane coupling agent hydrolyzate are refluxed for 2 hours at a mass volume ratio of 100:1 g / ml for 2 hours; filtered, washed with distilled water until neutral;
[0057] (2) 1g of 4,4'-bipyridyl was dissolved in 100ml of ethanol to obtain solution A;
[0058] (3) 5g 2,5-dihydroxybenzoic acid and 0.8g copper nitrate trihydrate were dissolved in 100ml water to obtain solution B;
[0059] (4) Add 0.2g of neutral attapulgite nanorod crystals prepared in step (1) into solution A, then slowly add solution B, and mix evenly with ultrasonic waves;
[0060] (5) Put the mixed solution obtained in step (4) into an autoclave, let stand at 200° C. for 20 hours, and filter to obtain green needle-shaped crystals;
[0061] (6) Heat the green needle-shaped crystals to 120° C., and vacuum-dry for 6 hours to prepare the finished adsorbent.
Embodiment 3
[0063] (1) Attapulgite nanorod crystals with a high aspect ratio greater than 20 and a silane coupling agent hydrolyzate are refluxed for 2 hours at a mass volume ratio of 75:1 g / ml and refluxed for 2 hours; filtered, washed with distilled water until neutral;
[0064] (2) 1g of 4,4'-bipyridyl was dissolved in 100ml of ethanol to obtain solution A;
[0065] (3) 5g 2,5-dihydroxybenzoic acid and 0.8g copper nitrate trihydrate were dissolved in 100ml water to obtain solution B;
[0066] (4) Add 0.2g of neutral attapulgite nanorod crystals prepared in step (1) into solution A, then slowly add solution B, and mix evenly with ultrasonic waves;
[0067] (5) Put the mixed solution obtained in step (4) into an autoclave, let stand at 180° C. for 24 hours, and filter to obtain green needle-shaped crystals;
[0068] (6) Heat the green needle-shaped crystals to 110° C., and vacuum-dry for 5 hours to prepare the finished adsorbent.
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