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Preparation method of ferrocene-modified Fenton catalyst for iron-based metal-organic framework material

A technology of iron-based metals and organic frameworks, applied in organic compound/hydride/coordination complex catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems that are rarely used in advanced oxidation processes, etc. Achieve low cost, mild reaction conditions, and environmental friendliness

Active Publication Date: 2017-12-29
UNIV OF JINAN
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Therefore, ferrocene is usually used as a redox mediator in electrochemical detection, biocatalysis, electrosynthesis, etc., but rarely used in advanced oxidation processes.

Method used

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  • Preparation method of ferrocene-modified Fenton catalyst for iron-based metal-organic framework material
  • Preparation method of ferrocene-modified Fenton catalyst for iron-based metal-organic framework material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] (1) Preparation of MIL-101(Fe)-Fc catalyst

[0022] NH 2 -Preparation of MIL-101(Fe): 0.675 g FeCl 3 ·6H 2 O and 0.224 g of 2-amino-terephthalic acid were dissolved in 15 mL of N, N-dimethylformamide (DMF), stirred at room temperature for 10 min, and then encapsulated in polytetrafluoroethylene In a lined reactor, react at 110 °C for 24 h, cool to room temperature; centrifuge, then heat-treat in 50 ml ethanol at 60 °C for 3 h, perform a total of two heat treatments to remove the adsorbed impurities, and finally in Dry in vacuum at 60 °C for 24 h.

[0023] Preparation of MIL-101(Fe)-Fc catalyst: 0.1 g NH 2 - Disperse MIL-101(Fe) in 15 mL ethanol, stir magnetically for 5 min; then add 0.0214 g ferrocene formaldehyde, then heat and reflux at 80 °C for 2 h; centrifuge, wash with ethanol and deionized water three times each , and finally dried under vacuum at 60 °C for 24 h.

[0024] (2) Catalyst performance evaluation

[0025] The organic pollutant bisphenol A was se...

Embodiment 2

[0028] (1) Preparation of MIL-53(Fe)-Fc catalyst

[0029] NH 2 - Preparation of MIL-53(Fe): 0.543 g of 2-aminoterephthalic acid was ultrasonically dispersed in 15 mL of DMF, and then 0.8109 g of FeCl was added 3 ·6H 2O, magnetically stirred for 15 min; reacted in a Teflon-lined autoclave at 150 °C for 5 h; cooled to room temperature, centrifuged, washed with water and ethanol, and finally vacuum-dried at 60 °C for 24 h to obtain NH 2 -MIL-53(Fe).

[0030] Preparation of MIL-53(Fe)-Fc catalyst: 0.1 g NH 2 -MIL-53(Fe) was dispersed in 15 mL of ethanol, stirred magnetically for 5 min; then added 0.0214 g of ferrocene formaldehyde, and then heated to reflux at 80 °C for 2 h; centrifuged, washed three times with ethanol and deionized water , and finally dried under vacuum at 60 °C for 24 h.

[0031] (2) Catalyst performance evaluation

[0032] The organic pollutant bisphenol A was selected as the probe molecule to study the performance of the prepared catalyst. Add 5 mg of c...

Embodiment 3

[0035] (1) Preparation of MIL-88B(Fe)-Fc catalyst

[0036] NH 2 -Preparation of MIL-88B(Fe): 0.379 g of 2-aminoterephthalic acid was ultrasonically dispersed in 15 mL of DMF and 1.2 mL of 2 mol / L NaOH mixed solution, and then 1.212 g of Fe(NO 3 ) 3 9H 2 O, magnetically stirred for 15 min; reacted in a polytetrafluoroethylene-lined autoclave at 100 °C for 12 h; cooled to room temperature, centrifuged, washed with water and ethanol, and finally vacuum-dried at 60 °C for 24 h.

[0037] Preparation of MIL-88B(Fe)-Fc catalyst: 0.1 g NH 2 -MIL-88B(Fe) was dispersed in 15 mL ethanol, stirred magnetically for 5 min; then added 0.0214 g ferrocene formaldehyde, and then heated to reflux at 80 °C for 2 h; centrifuged, washed three times with ethanol and deionized water , and finally dried under vacuum at 60 °C for 24 h.

[0038] (2) Catalyst performance evaluation

[0039] The organic pollutant bisphenol A was selected as the probe molecule to study the performance of the prepared ...

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Abstract

The invention discloses a preparation method of a ferrocene-modified Fenton catalyst for an iron-based metal-organic framework material. The preparation method comprises the following steps of firstly, synthesizing amino-containing iron-based metal-organic framework material (NH2-MIL(Fe)) by a solvent thermal method; then, enabling the amino group in the NH2-MIL(Fe) and the carbanyl group in ferrocenecarboxaldehyde to generate condensation function by a post-modifying method, and immobilizing ferrocene onto the NH2-MIL(Fe), so as to prepare the MIL(Fe)-Fc catalyst. The catalyst has the advantages that the catalyzing activity is high, the environment-friendly effect is realized, the recycling is easy, the reutilization effect is realized, the organic pollutants in water can be efficiently degraded in the wider pH (potential of hydrogen) range, and the application prospect is larger.

Description

technical field [0001] The invention belongs to the field of wastewater treatment, and in particular relates to a method for preparing a ferrocene-modified iron-based metal-organic framework material-like Fenton catalyst. Background technique [0002] The advanced oxidation technology based on sulfate radicals has been developed rapidly in recent years. It uses persulfate (S 2 o 8 2− ) as an oxidant, which can be catalytically decomposed in a variety of ways to generate highly oxidative sulfate radicals (SO 4 −• ), for example, activation methods such as ultraviolet light, heat, transition metals, etc. Among these activation methods, the catalytic activity of homogeneous iron or cobalt salts is greatly affected by the pH value, which cannot be recycled and has potential toxicity. Therefore, heterogeneous catalysts such as Fe 3 o 4 、Co 3 o 4 become a research hotspot. where Fe 3 o 4 It is a heterogeneous Fenton-like catalyst with excellent performance, which can c...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J31/22C02F1/00C02F101/34
CPCB01J31/1691B01J2531/0225B01J2531/0252B01J2531/842C02F1/00C02F2101/345
Inventor 王钰国伟林郭怀苏王瑞芹韩凤卫静
Owner UNIV OF JINAN