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Dendrimer functionalized mesoporous material as well as preparation method and application thereof

A technology of dendritic molecules and mesoporous materials, applied in chemical instruments and methods, energy wastewater treatment, ion exchange water/sewage treatment, etc., to achieve good stability, excellent regeneration performance, reusability, and high specific surface area

Active Publication Date: 2022-06-03
DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there are no reports on dendrimer functionalized mesoporous materials with strong anion exchange function and their application in the removal of non-steroidal anti-inflammatory drugs in water.

Method used

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  • Dendrimer functionalized mesoporous material as well as preparation method and application thereof
  • Dendrimer functionalized mesoporous material as well as preparation method and application thereof
  • Dendrimer functionalized mesoporous material as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] The preparation method of the G1 dendrimer functionalized mesoporous material for rapidly and efficiently removing NSAIDs in water comprises the following steps:

[0034] (1) Dissolve 13.8g P123 and 7.6g mass concentration 35% concentrated hydrochloric acid in 250mL water, fully stir until P123 is completely dissolved until transparent, add 24.8g ethyl orthosilicate dropwise under vigorous stirring, the mixed solution is at 35 ℃ water bath with continuous stirring for 12h. The mixture was then transferred into a reaction kettle and hydrothermally treated at 130 °C for 24 h. The resulting white precipitate was filtered and washed repeatedly with water. Finally, the product was calcined at 550 °C for 2 h to obtain large-pore SBA-15; the obtained SBA-15 was soaked in 3 mol / L hydrochloric acid solution overnight, and then dewatered and activated at 160 °C for 6 h;

[0035](2) Disperse 4g of the above activated SBA-15 in 110mL of anhydrous toluene, add 4mL of 3-aminopropyl...

Embodiment 2

[0038] A preparation method of a G2 dendrimer functionalized mesoporous material for rapidly and efficiently removing non-steroidal anti-inflammatory drugs in water, comprising the following steps:

[0039] (1) The same as step (1) in Example 1, SBA-15 was obtained.

[0040] (2) same as step (2) in embodiment 1, obtain NH 2 -SBA-15.

[0041] (3) The same as step (3) in Example 1, a half-generation dendrimer functionalized G0.5-SBA-15 was obtained. G0.5-SBA-15 was placed in 100 mL of 80% methanol aqueous solution, 0.6 g of methylamine was added, and the reaction was refluxed at 80 °C for 4 h. The above reaction solution was filtered, washed with methanol and acetone in turn, and vacuum-dried at 60°C for 3 hours to obtain a dendrimer with a secondary amine as an end group. G2-SBA-15 was synthesized by the quaternization end-capping reaction of amines.

Embodiment 3

[0043] A preparation method of a G3 dendrimer functionalized mesoporous material for rapidly and efficiently removing non-steroidal anti-inflammatory drugs in water, comprising the following steps:

[0044] (1) The same as step (1) in Example 1, SBA-15 was obtained.

[0045] (2) same as step (2) in embodiment 1, obtain NH 2 -SBA-15.

[0046] (3) Same as step (3) in Example 2, obtain 1.5-generation dendrimer functionalized G1.5-SBA-15. Put G1.5-SBA-15 in 100 mL of 80% methanol aqueous solution, add 1.2 g Methylamine was refluxed at 80°C for 4h. The above reaction solution was filtered, washed with methanol and acetone in turn, and vacuum-dried at 60°C for 3 hours to obtain a dendrimer with a secondary amine as an end group. G3-SBA-15 was synthesized by quaternization end-capping reaction of amines.

[0047] see attached figure 2 The TEM image of G3-SBA-15 in the dendrimer-functionalized mesoporous silicon still maintains a highly ordered pore structure, which will be very...

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Abstract

The invention discloses a dendrimer functionalized mesoporous material for rapidly and efficiently removing non-steroidal anti-inflammatory drugs in water and a preparation method of the dendrimer functionalized mesoporous material, and belongs to the field of water purification functional materials. The preparation method comprises the following steps: aminating large-aperture mesoporous silicon synthesized by copolycondensation to obtain amino-functionalized mesoporous silicon, and alternately carrying out multiple repeated nucleophilic ring-opening reactions with resorcinol diglycidyl ether and methylamine by using an amino group on the mesoporous silicon as a core through a divergent method to obtain a half-generation dendrimer Gn-0. 5 with an epoxy group as a terminal group. The Gn-0. 5 and micromolecule tertiary amine are further subjected to an end capping reaction, and the whole-generation dendrimer Gn with the quaternary ammonium cation as the end group is prepared. The dendrimer functionalized mesoporous material prepared by the invention not only has the advantages of high specific surface area and rapid mass transfer of an ordered mesoporous material and high density of dendrimer functional groups, but also has the hydrophobic effect of phenyl and the strong anion exchange function of quaternary ammonium, and has the advantages of high adsorption rate, high adsorption capacity and strong selectivity to organic anions; the method is suitable for rapidly and efficiently removing anionic drugs such as non-steroidal anti-inflammatory drugs in water.

Description

technical field [0001] The invention relates to the field of water purification functional materials, in particular to a dendrimer functionalized mesoporous material for rapidly and efficiently removing non-steroidal anti-inflammatory drugs from water, and a preparation method and application thereof. Background technique [0002] Non-steroidal anti-inflammatory drugs (NSAIDs) are a class of antipyretic, analgesic and anti-inflammatory drugs commonly used in clinical practice. The use of NSAIDs in my country is increasing year by year, and the amount of NSAIDs is close to that of antibiotics. Commonly used are ibuprofen, diclofenac and naphthalene. Pusheng et al. In recent years, NSAIDs pollutants have been detected in sewage, surface water, groundwater and drinking water all over the world, and have been proved to have certain hazards to the ecological environment and human health. In 2012, the European Commission listed diclofenac as a new One of the 12 priority pollutants...

Claims

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Application Information

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IPC IPC(8): C08G83/00C02F1/28C02F1/42C02F101/30
CPCC08G83/003C08G83/004C02F1/285C02F1/42C02F2001/422C02F2101/30Y02W10/37
Inventor 李云齐亚·阿曼德张亦弛陈吉平
Owner DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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