Ozone heterogeneous oxidation solid catalyst preparation method

A heterogeneous oxidation, solid catalyst technology, used in catalyst activation/preparation, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc. The problem of low catalyst adsorption can achieve strong adsorption, improve anti-toxicity and catalytic activity, and inhibit the effect of precipitation.

Inactive Publication Date: 2017-08-18
SICHUAN NORMAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In view of the problems of low catalyst adsorption, poor anti-toxicity and easy loss of catalytic activity in the current preparation method of ozone heterogeneous oxidation solid catalyst, a multi-component porous carrier was developed to enhance the adsorption of the catalyst through pore expansion and surface activation. Rare earth metal organic compounds as precursors of catalytic active additives, common transition metal organic compounds and noble metal compounds as precursors of catalytic active centers and multi-component porous carriers through hydrothermal reaction and high temperature calcination to prepare ozone heterogeneous oxidation containing multiple metals The preparation method of solid catalyst to improve the anti-toxicity and catalytic activity of the catalyst is characterized in that component A and deionized water are added into a sealable reactor and stirred to prepare an aqueous solution, and the weight concentration of component A is controlled to be 2% to 6%. After the preparation is completed, add component B under stirring, raise the temperature to 35°C-50°C, continue to stir

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0007] Embodiment 1:1.35g lithium hypochlorite, 1.65g bis(acetylacetonate) beryllium, 140ml deionized water, join volume and be that in the sealable reactor of 500ml, stir and mix evenly, the weight concentration of this aqueous solution is 2.1%, times Lithium chlorate: bis(acetylacetonate) beryllium weight ratio = 1:1.2; add deionized water to wash to neutral, dry at 103°C to remove moisture, and then sieve -200 mesh to +400 mesh standard sieve 2.75g γ-oxidized Weight of aluminum, 3.75g barite, 4.75g fluorite, 5.75g glauberite, 6.75g hydrotalcite, 7.75g alunite, lithium hypochlorite and bis(acetylacetonate)beryllium (3g): weight of porous material ( 31.5g) = 1:10.5, heat up to 36°C, continue stirring for 3.2h, filter, dry at 103°C and obtain 31g of pore-enlarging modified carrier; put 31g of pore-enlarging modified carrier into a 500ml ultrasonic reactor, Then add 3.25g dimethyl dioctadecyl ammonium chloride and be dissolved in the aqueous solution of 100ml deionized water, t...

Embodiment 2

[0008] Embodiment 2: 0.24g lithium hypochlorite, 0.36g bis(acetylacetonate) beryllium, 10ml deionized water, join volume and be that in the sealable reactor of 100ml, stir and mix evenly, the weight concentration of this aqueous solution is 5.7%, times Lithium chlorate: bis(acetylacetonate) beryllium weight ratio = 1:1.5; add deionized water to wash to neutral, dry at 103°C to remove moisture, and then sieve -200 mesh to +400 mesh standard sieve 1.45g gamma-oxidized Weight of aluminum, 1.65g barite, 1.85g fluorite, 2.05g glauberite, 2.25g hydrotalcite, 2.45g alunite, lithium hypochlorite and bis(acetylacetonate)beryllium (0.6g): weight of porous material (11.7g)=1:19.5, heat up to 48°C, continue to stir for 5.8h, filter, dry at 105°C and obtain 11.5g of pore-enlarging modified carrier; in a 100ml ultrasonic reactor, put the pore-enlarging modified carrier 11.5g, then add 2.2g dimethyl dioctadecyl ammonium chloride and dissolve in 26ml deionized water, the weight concentration ...

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Abstract

The invention belongs to the technical field of environment protection and chemical catalysts and relates to an ozone heterogeneous oxidation solid catalyst preparation method. The preparation method includes: taking porous mineral materials including gamma-aluminum oxide, barite, fluorite, glauberite, hydrotalcite and alunite as carriers; subjecting the carriers to lithium hypochlorite and bis(acetylacetone)beryllium broaching modification; adding surfactant dioctadecyldimethyl ammonium chloride for surface activation under the action of ultrasonic waves; subjecting the carriers to hydrothermal reaction, with a complex mineralizer composed of borax and potassium sulfate, catalytic activity auxiliary agent precursors including tetra(2,2,6,6-tetramethyl-3,5-hydrochelidonic acid)cerium (IV), terbium acetate hydrate and tri(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octenyldiketone)dysprosium (III) and catalytic activity central precursors including lysine manganese, L-aspartic acid molybdenum, tetraammine dichloropalladium and cis-dichlorodiamineplatinum, in a hydrothermal reactor under the action of tri(cetyl)methyl ammonium bromide serving as an emulsifying agent; drying to remove moisture, and firing in a muffle furnace at a certain temperature to obtain an ozone heterogeneous oxidation solid catalyst.

Description

technical field [0001] The invention relates to a preparation method of a solid catalyst for ozone heterogeneous oxidation, which belongs to the technical fields of environmental protection and chemical catalysts. Background technique [0002] Ozone oxidation technology utilizes the strong oxidation ability of ozone, which can oxidize and decompose many organic pollutants, and is widely used in wastewater treatment. Ozone catalytic oxidation technology is divided into ozone homogeneous catalytic oxidation and ozone heterogeneous catalytic oxidation. Ozone homogeneous catalytic oxidation has catalysts that are difficult to separate, recycle and reuse, and the low utilization rate of ozone leads to high water treatment operation costs. Ozone heterogeneous catalytic oxidation technology has the advantages of easy separation and recovery of catalysts and reusable use, high ozone utilization rate, and high removal rate of organic pollutants, which reduces water treatment. The ad...

Claims

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Application Information

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IPC IPC(8): B01J23/656B01J32/00B01J20/20B01J20/30C02F1/28C02F1/78C02F101/30
CPCB01J23/6562B01J20/0248B01J20/0281B01J20/045B01J20/046B01J20/06B01J20/08B01J20/20B01J35/10B01J37/084B01J37/10B01J2220/42B01J2220/4806B01J2220/4812C02F1/281C02F1/725C02F1/78C02F2101/30C02F2305/02
Inventor 朱明范耀月石小阳
Owner SICHUAN NORMAL UNIVERSITY
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