Preparation method of magnetic mesoporous free radical controlled polymer ion printing adsorbing agent
A technology of ion imprinting and free radicals, applied in chemical instruments and methods, alkali metal compounds, alkali metal oxides/hydroxides, etc., can solve problems that have not been reported yet
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Embodiment 1
[0032] (1) Synthesis of magnetic mesoporous SBA-15 (Fe 3 o 4 SBA-15)
[0033] Weigh 0.1 g Fe(NO 3 ) 3 9H 2 Dissolve O in 5 mL of methanol, continue to add 0.1 g of SBA-15, stir well until the mixture is uniform, and then place it in an oven at 80°C for drying. The solid obtained after drying was fully ground into powder, exposed to acetic acid vapor at 80 °C for 1 h, and then dried in the open at 80 °C to remove physically adsorbed acetic acid molecules. Finally, put the dried orange-yellow powder into the tube furnace, N 2 Under protection, the temperature was programmed to rise to 400°C at 5°C / min and kept for 20 minutes to obtain Fe-doped 3 o 4 particles of magnetic mesoporous SBA-15 (Fe 3 o 4 SBA-15).
[0034] (2) Benzylated Fe on the surface 3 o 4 Preparation of SBA-15 (Fe 3 o 4 SBA-15-Cl)
[0035] Take 0.1 g Fe synthesized in the above step (1) 3 o 4 Disperse SBA-15 in 10 mL of anhydrous toluene, continue to add 0.1 mL of 4-chloromethyl-phenyltri...
Embodiment 2
[0046] (1) Synthesis of magnetic mesoporous SBA-15 (Fe 3 o 4 SBA-15)
[0047] Weigh 0.2 g Fe(NO 3 ) 3 9H 2 Dissolve O in 5 mL of methanol, continue to add 0.1 g of SBA-15, stir well until the mixture is uniform, and then place it in an oven at 80°C for drying. The solid obtained after drying was fully ground into powder, exposed to acetic acid vapor at 80 °C for 1 h, and then dried in the open at 80 °C to remove physically adsorbed acetic acid molecules. Finally, put the dried orange-yellow powder into the tube furnace, N 2 Under protection, the temperature was raised to 400°C at a rate of 5°C / min and kept for 20 min to obtain Fe-doped 3 o 4 particles of magnetic mesoporous SBA-15 (Fe 3 o 4 SBA-15).
[0048] (2) Benzylated Fe on the surface 3 o 4 Preparation of SBA-15 (Fe 3 o 4 SBA-15-Cl)
[0049] Take 0.3 g Fe synthesized in the above step (1) 3 o 4 SBA-15 was dispersed in 15 mL of anhydrous toluene, and 0.3 mL of 4-chloromethyl-phenyltrimethoxysilane...
Embodiment 3
[0060] (1) Synthesis of magnetic mesoporous SBA-15 (Fe 3 o 4 SBA-15)
[0061] Weigh 0.4 g Fe(NO 3 ) 3 9H 2 Dissolve O in 5 mL of methanol, continue to add 0.1 g of SBA-15, stir well until the mixture is uniform, and then place it in an oven at 80°C for drying. The solid obtained after drying was fully ground into powder, exposed to acetic acid vapor at 80 °C for 1 h, and then dried in the open at 80 °C to remove physically adsorbed acetic acid molecules. Finally, put the dried orange-yellow powder into the tube furnace, N 2 Under protection, the temperature was raised to 400°C at a rate of 5°C / min and kept for 20 min to obtain Fe-doped 3 o 4 particles of magnetic mesoporous SBA-15 (Fe 3 o 4 SBA-15).
[0062] (2) Benzylated Fe on the surface 3 o 4 Preparation of SBA-15 (Fe 3 o 4 SBA-15-Cl)
[0063] Take 0.7 g Fe synthesized in the above step (1) 3 o 4 SBA-15 was dispersed in 25 mL of anhydrous toluene, and 0.625 mL of 4-chloromethyl-phenyltrimethoxysilane...
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