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Method of preparation of solid catalyst by ozone heterogeneous oxidation

A heterogeneous oxidation, solid catalyst technology, applied in the direction of catalyst activation/preparation, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problems of poor toxicity resistance, low catalyst adsorption, It is easy to lose catalytic activity and other problems, and achieve the effect of strong adsorption, inhibition of melting and precipitation, and improvement of anti-toxicity and catalytic activity

Inactive Publication Date: 2017-08-25
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 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

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Embodiment 1

[0007] Example 1: 1.35g lithium hypochlorite, 1.65g bis(acetylacetonate) beryllium, 140ml deionized water, were added to a sealable reactor with a volume of 500ml, stirred and mixed, and the weight concentration of the aqueous solution was 2.1%, the time Lithium chlorate: bis(acetylacetonate) beryllium weight ratio = 1:1.2; add deionized water to wash to neutrality, dry at 103 ° C to remove moisture, sieve 2.75g diatoms with -200 mesh ~ +400 mesh standard sieve Pure, 3.75g kyanite, 4.75g fluorite, 5.75g glauberite, 6.75g sodium saltpeter, 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, and dry at 103°C to obtain 31g of modified pore-enlarging carrier; in a 500ml ultrasonic reactor, put 31g of pore-enlarging modified carrier, Then add an aqueous solution of 3.25g monoalkyl ether trimethyl ammonium chloride dissolved in 100ml deionized water, ...

Embodiment 2

[0008] Example 2: 0.24g lithium hypochlorite, 0.36g bis(acetylacetonate) beryllium, 10ml deionized water were added to a sealable reactor with a volume of 100ml and stirred and mixed uniformly. The weight concentration of the aqueous solution was 5.7%. Lithium chlorate: bis(acetylacetonate) beryllium weight ratio = 1:1.5; add deionized water to wash to neutrality, dry at 103 ° C to remove moisture, sieve -200 mesh ~ +400 mesh standard sieve 1.45g diatom Weight of pure, 1.65g kyanite, 1.85g fluorite, 2.05g glauberite, 2.25g sodium saltpeter, 2.45g dolomite, 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 and react for 5.8h, filter, and dry at 105°C to obtain 11.5g of modified pore-enlarging carrier; in a 100ml ultrasonic reactor, put into the pore-enlarging modified carrier 11.5g, then add 2.2g of monoalkyl ether trimethyl ammonium chloride dissolved in 26ml of deionized water solution, ...

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Abstract

The invention relates to a method of preparation of solid catalyst by ozone heterogeneous oxidation, belongs to the technical field of environmental protection and chemical engineering catalysts. Diatom pure, kyanite, fluorite, glauberite, nitratine and dolomite are adopted as carriers after subjecting to bore-reaming by lithium hypochlorite and di-(acetylacetone) beryllium, activating treatment is conducted by the subjoining of surfactant mono alkyl ether trimethyl ammonium chloride under the action of ultrasonic waves, then the carriers are subject to hydrothermal reaction in a hydrothermal reaction kettle with a composite mineralizer borax and potassium sulfate, precursors of catalytic coagent tri-(acetylacetonate hexafluoride) yttrium (III) dihydrate, tricyclic cyclopentadienyl promethium, tri-(2, 2, 6, 6-tetramethyl-3, 5-pimelic ketonic acid) gadolinium, tri-[N, N-di-(trimethylsilyl) amine] erbium, catalytic active core precursor of pyruvic acid isonicotinoyl hydrazone vanadium, cobalt gluconate, and di-thiocyanate radical combined silver (I) potassium acid, dichloro-diamine platinum under the action of emulsifier stearamide propyl dimethylamine lactate, after stoving, the moisture content is removed, and a solid catalyst by ozone heterogeneous oxidation is obtained by firing in a muffle furnace.

Description

technical field [0001] The invention relates to a preparation method of an ozone heterogeneous oxidation solid catalyst, belonging to the technical field of environmental protection and chemical catalysts. Background technique [0002] Ozone oxidation technology utilizes the characteristics of strong ozone oxidation ability, 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. Low ozone utilization leads to high operating costs for water treatment. At the same time, organic pollutants are removed. The low rate and easy to cause secondary pollution of water body limit its application; the ozone heterogeneous catalytic oxidation technology has the advantages of easy separation, recovery and reus...

Claims

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Application Information

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IPC IPC(8): B01J23/89B01J32/00B01J20/20B01J20/30C02F1/28C02F1/78C02F101/30
CPCB01J20/04B01J20/043B01J20/045B01J20/046B01J20/06B01J20/103B01J20/14B01J20/20C02F1/281C02F1/725C02F1/78B01J23/898B01J37/084B01J37/10C02F2101/30C02F2305/02B01J2220/4812B01J2220/42B01J2220/4806B01J35/60
Inventor 朱明刘阳魏玉君
Owner SICHUAN NORMAL UNIVERSITY
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