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Method for preparing ozone heterogeneous oxidized solid catalyst

A heterogeneous oxidation, solid catalyst technology, applied in heterogeneous catalyst chemical elements, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problem of poor anti-toxicity, catalyst adsorption Low, easy to lose catalytic activity and other problems, to achieve strong adsorption, inhibit precipitation, improve anti-toxicity and catalytic activity.

Inactive Publication Date: 2017-08-15
SICHUAN NORMAL UNIVERSITY
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  • Abstract
  • Description
  • Claims
  • Application Information

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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 for 3h-6h, filter, and dry the reaction product at 102°C-106°C to obtain a modified carrier for pore expansion; pore expansion Put the modified carrier into the ultrasonic reactor, add the aqueous solution prepared by C component and deionized water, the weight concentration of C component is 3%~8%, stir and mix evenly, control the ultrasonic power density to 0.3~0.8W / m 3 , frequency 20kHz ~ 30kHz, 40 ℃ ~ 55 ℃, ultrasonic vibration 2h ~ 5h, the ultrasonic surface activation carrier mixture is obtained; the ultrasonic surface activation carrier mixture is transferred to the hydrothermal reaction kettle, and then add D component and deionized water to prepare The aqueous solution, the weight concentration of D component is 40% ~ 55%, by weight, the weight ratio of D component deionized aqueous solution: ultrasonic surface activation carrier mixture = 1: (1.5 ~ 2), control temperature 120 ℃ ~ 180°C, the hydrothermal reaction time is 8h~16h, and then dried to obtain fine particles; the fine particles are burned in a muffle furnace at 600°C~950°C for 3h~8h to obtain a solid catalyst for ozone heterogeneous oxidation

Method used

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Examples

Experimental program
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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: the weight ratio of bis(acetylacetonate) beryllium=1:1.2; add deionized water to wash to neutral, dry at 103°C to remove moisture, and then sieve 2.75g diatoms of -200 mesh to +400 mesh standard sieve Pure, 3.75g kyanite, 4.75g hydrotalcite, 5.75g alunite, 6.75g soda saltpetre, 7.75g dolomite, weight of 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 of dodecyl dimethyl hydroxyethyl ammonium chloride and dissolve it in 100ml of deionized water. The w...

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: the weight ratio of bis(acetylacetonate) beryllium=1:1.5; add deionized water to wash to neutral, dry at 103°C to remove moisture, and then sieve 1.45g diatoms of -200 mesh to +400 mesh standard sieve Pure, 1.65g kyanite, 1.85g hydrotalcite, 2.05g alunite, 2.25g sodium saltpeter, 2.45g dolomite, weight of 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 of dodecyl dimethyl hydroxyethyl ammonium chloride and dissolve in 26ml deionized water, the weight...

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Abstract

The invention relates to a method for preparing an ozone heterogeneous oxidized solid catalyst, which belongs to the technical fields of environmental protection and a chemical catalyst. The preparation method comprises the following steps: diatom pure, kyanite, hydrotalcite, alum stone, nitratine and dolostone are taken as carriers, the carriers are subjected to hole-reaming modification through lithium hypochlorite and dis(acetylacetone)beryllium, a surfactant dodecyl dimethyl hydroxyethyl ammonium chloride is added, surface activation treatment is carried out under supersonic wave effect, then the carriers after ultrasonic surface activation are subjected to a hydro-thermal reaction with a composite mineralizer borax and potassium sulfate, a catalytic activity auxiliary agent predecessor tri(hexafluoroacetylacetone)yttrium (III)dehydrate, tricyclopentadiene promethium, tri(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octylene dione)dysprosium (III), tri(trifluoromethanesulfonimide)ytterbium, a catalytic activity central composite predecessor common transition metallorganic compound pyruvate iso-nicotinoylhydrazone vanadium, cobalt gluconate and hexanitro rhodium trisodium, dipotassium hexachloroosmium in a hydro-thermal reaction vessel under effect of an emulsifier dioctadecalkyl ammonium bromide, the reaction products are dried to remove the moisture, in a muffle furnace, and the product is calcinated to obtain the ozone heterogeneous oxidized 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): B01J23/89B01J32/00C02F1/28C02F1/78C02F101/30
CPCC02F1/281C02F1/725C02F1/78B01J23/002B01J23/898C02F2101/30B01J2523/00B01J35/40B01J35/50B01J2523/36B01J2523/3731B01J2523/3762B01J2523/3787B01J2523/55B01J2523/845B01J2523/822B01J2523/825
Inventor 朱明刘阳魏玉君
Owner SICHUAN NORMAL UNIVERSITY
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