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SiO2@MIL-88A core-shell material for degrading organic printing and dyeing waste and preparation process of SiO2@MIL-88A core-shell material

A core-shell and waste technology, applied in the fields of material engineering and photocatalytic degradation, to achieve the effects of high catalytic activity, mild preparation conditions and large specific surface area

Pending Publication Date: 2021-12-21
SHANGHAI NORMAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, how to use the porous structure, high catalytic activity, and efficient ligand-metal charge transfer (LMCT) characteristics of MOF materials to construct green and efficient photolytic water purification materials urgently needs to be explored.

Method used

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  • SiO2@MIL-88A core-shell material for degrading organic printing and dyeing waste and preparation process of SiO2@MIL-88A core-shell material
  • SiO2@MIL-88A core-shell material for degrading organic printing and dyeing waste and preparation process of SiO2@MIL-88A core-shell material
  • SiO2@MIL-88A core-shell material for degrading organic printing and dyeing waste and preparation process of SiO2@MIL-88A core-shell material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0103] a. Take 50mL n-propanol, 15.2mL H 2 O, 4.75mL of ammonia water was added to the reaction flask in turn, cooled, stirred at 450rpm, 13mL of tetraethyl silicate in propanol (0.23mL / L) was added dropwise, and reacted for 30min to obtain silicon ball seed solution.

[0104] b. Take 5mL of the above-mentioned seed liquid mixed by ultrasonic, 25mL of propanol, 5.7mL of H 2 0. Add 4mL ammonia water to a 250mL eggplant-shaped flask successively (keep the stirring speed at 450rpm). Continue to add 16mL of ammonia water at 25°C, use a syringe pump, add 59mL of 0.23mol / L tetraethyl silicate / propanol solution at 30mL / h, after the addition is complete (about 2h), slowly reduce the speed to 350rpm, and stir overnight ( 8h or more). Suction filtration to obtain silica spheres, which were washed with water and ethanol in turn, and then vacuum-dried at 55°C for 12 hours for use.

[0105] c, take 500mg of the above SiO 2 The spheres were dispersed in 50mL of ethanol, and refluxed at ...

Embodiment 2

[0108] a, take 50mL n-propanol, 15mL H 2 0, 5mL of ammonia water were sequentially added to the reaction flask, the temperature was lowered, stirred at 520rpm, 15mL of tetraethyl silicate in propanol (0.23mL / L) was added dropwise, and reacted for 40min to obtain silicon ball seed solution.

[0109] b. Take 5mL of the above seed liquid mixed by ultrasonic, 25mL of propanol, 6mL of H 2 0. Add 4.5mL ammonia water to a 250mL eggplant-shaped flask in turn (keep the stirring speed at 450rpm). Continue to add 18mL of ammonia water at 25°C, use a syringe pump, add 60mL of 0.22mol / L tetraethyl silicate / propanol solution at 28mL / h, after the addition is complete (about 2h), slowly reduce the speed to 3300rpm, and stir overnight ( 8h or more). Suction filtration to obtain silica spheres, which were washed with water and ethanol in turn, and then vacuum-dried at 60°C for 12 hours for use.

[0110] c, take 550mg of the above SiO 2 The spheres were dispersed in 50mL of ethanol and reflu...

Embodiment 3

[0113] First, accurately weigh 50.0 mg of acid red (AR-18) into a 50.0 mL volumetric flask, add deionized water to volume, and prepare a 1.0 mg / mL dye solution. The test system is 1.0mL of dye solution, 1.03mL of 30% hydrogen peroxide, 50.0mL of deionized water (at this time, the concentration of dye is about 20mg / L, and the concentration of hydrogen peroxide is about 10mmol / L), after adding 20mg of SiO 2 @MIL-88A core-shell catalyst, stirred under sunlight, and started timing, took about 2mL of samples every 10 minutes, and measured its UV-Vis absorption spectrum. It can be seen that the UV absorption spectrum intensity of AR-18 gradually weakens with time ( Figure 4 ), the reaction solution turns from red to colorless, and its degradation rate (R) reaches 85% in 20min after calculation ( Figure 9 ).

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Abstract

The invention discloses a SiO2@MIL-88A core-shell material for degrading organic printing and dyeing waste and a preparation process thereof. The preparation method comprises the following steps: (1) by taking a silicon dioxide sphere as a carrier, modifying a carboxylic acid functional group on the surface of the silicon sphere through 3-aminopropyltriethoxysilane and succinic anhydride; and (2) adding carboxylic acid silicon balls into a reaction solution for synthesizing the MIL-88A through an in-situ synthesis method, and loading the MOFs crystal (MIL-88A) on the silicon balls under the coordination action of carboxylic acid, thereby obtaining the SiO2@MIL-88A core-shell material.

Description

technical field [0001] The invention relates to the technical field of material engineering and photocatalytic degradation, in particular to a core-shell material—SiO2, which is a metal-organic framework material (MOFs) wrapped with silicon dioxide for degrading organic printing and dyeing waste. 2 @MIL-88A and its preparation process. Background technique [0002] With the rapid development of industry and economy, the shortage of water resources and the pollution of water environment are serious problems affecting the sustainable development of human society. Among them, the high pollution characteristics of the textile printing and dyeing industry have always attracted the attention of environmental protection. In recent years, great efforts have been made in developing effective technologies to mitigate water pollution, and methods including adsorption, biological treatment, membrane separation, and advanced oxidation have been widely used in wastewater treatment. Amon...

Claims

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Application Information

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IPC IPC(8): B01J31/22B01J35/00C02F1/30C02F1/72C02F101/30
CPCB01J31/1633B01J31/1691B01J31/2239C02F1/725C02F1/722C02F1/30B01J2531/842C02F2305/026C02F2305/10C02F2101/308B01J35/397
Inventor 谭春霞刘国华刘凯泓程探宇刘锐
Owner SHANGHAI NORMAL UNIVERSITY
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