Preparation method of ozone heterogeneous oxidation 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 resistance to toxicity and easy loss of catalysis Activation, low catalyst adsorption and other problems, to achieve strong adsorption, improve anti-toxicity and catalytic activity, inhibit the effect of precipitation

Inactive Publication Date: 2017-07-28
SICHUAN NORMAL UNIVERSITY
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  • Abstract
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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
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 2.75g attapulgite of -200 mesh to +400 mesh standard sieve Weight of soil, 3.75g diopside, 4.75g talc, 5.75g sodaite, 6.75g aluminum hydroxide, 7.75g lapis lazuli, lithium hypochlorite and bis(acetylacetonate)beryllium (3g): weight of porous material (31.5g)=1:10.5, heat up to 36°C, continue to stir 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 trioctylmethylammonium chloride and dissolve in 100ml of deionized water. The weight concentration of ...

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 1.45g attapulgite of -200 mesh to +400 mesh standard sieve Weight of soil, 1.65g diopside, 1.85g talc, 2.05g sodaite, 2.25g aluminum hydroxide, 2.45g lapis lazuli, lithium hypochlorite and bis(acetylacetonate)beryllium (0.6g): Porous material Weight (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-expanding modified carrier; put into 100ml ultrasonic reactor Carrier 11.5g, then add 2.2g of trioctylmethylammonium chloride dissolved in 26ml of deionized water aqueous solution, the weight concentration of the aqueous so...

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Abstract

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. The preparation method is to use attapulgite, diopside, talc, crystal soda, aluminum hydroxide and lapis lazuli porous materials as carriers, and after the carrier is modified by lithium hypochlorite and bis(acetylacetonate) beryllium to expand pores, add The surface active agent trioctylmethyl ammonium chloride is subjected to surface activation treatment under the action of ultrasonic waves, and then the ultrasonic surface activation carrier is mixed with the composite mineralizer borax and potassium sulfate in a hydrothermal reaction kettle, and the catalytic activity auxiliary agent precursor three (3 ‑Trifluoroacetyl‑D‑camphor) praseodymium (III), promethium tricyclopentadienyl, terbium triacetate hydrate, holmium oxalate decahydrate rare earth organometallic compound, catalytic active center component precursor common transition metal organic compound fuma Iron ferrous acid, nickel citrate and noble metal compound silver dithiocyanate (I) potassium, terpyridyl ruthenium chloride hexahydrate, hydrothermal under the action of emulsifier trimethylaminoethanol stearate ammonium iodide After the reaction, the reaction product is dried to remove moisture, and burned at a certain temperature in a muffle furnace to obtain a solid catalyst for ozone heterogeneous oxidation.

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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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/89B01J32/00C02F1/28C02F1/78C02F101/30
CPCB01J23/002B01J23/894B01J35/023B01J35/026B01J2523/00C02F1/281C02F1/725C02F1/78C02F2101/30
Inventor 朱明刘阳宋佳柠
Owner SICHUAN NORMAL UNIVERSITY
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