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Preparation method of ozone heterogeneous oxidized solid catalyst

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

Inactive Publication Date: 2017-08-08
SICHUAN NORMAL UNIV
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  • Summary
  • 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
Comparison scheme
Effect test

Embodiment 1

[0008] 1.35g lithium hypochlorite, 1.65g two (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%, lithium hypochlorite: 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 sieve -200 mesh to +400 mesh standard sieve 2.75g medical stone, 3.75g Weight of wollastonite, 4.75g potassium feldspar, 5.75g boronite, 6.75g fly ash, 7.75g coal gangue, lithium hypochlorite and bis(acetylacetonate) beryllium (3g): weight of porous material (31.5 g)=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, and then Add 3.25g of octadecyltrimethylammonium chloride and dissolve in 100ml deionized water, the weight concentration of the aq...

Embodiment 2

[0010] 0.24g lithium hypochlorite, 0.36g two (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%, lithium hypochlorite: 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 sieve 1.45g of medical stone, 1.65g of -200 mesh to +400 mesh standard sieve Weight of wollastonite, 1.85g potassium feldspar, 2.05g boronite, 2.25g fly ash, 2.45g coal gangue, 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 11.5g of pore-enlarging modified carrier g, then add 2.2g of octadecyltrimethylammonium chloride and be dissolved in 26ml deionized water aqueous solution, the w...

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Abstract

The invention relates to a preparation method of an ozone heterogeneous oxidized solid catalyst, and belongs to the technical field of environmental protection and chemical catalyst. The preparation method comprises the following steps: taking maifanite, wollastonite, potassium feldspar, szaibelyite, coal ash and coal gangue as carriers, performing lithium hypochlorite and bis(acetylacetonato) beryllium reaming, adding octadecyl trimethyl ammonium chloride to perform activating treatment under an ultrasonic effect; and then enabling the active carriers to perform hydrothermal reaction with the compound mineralizing agent borax and potassium sulfate, catalytic active promoter precursors yttrium tri(hexafluoroacetylacetone) (III) dihydrate, lanthanum stearate, cerium(IV)-2,2,6,6-tetramethylheptanedionate, erbium tris[bis(trimethylsilyl)amide], catalytic active center precursors titanocene ring substituted salicylic complex, L-aspartic acid molybdenum, sodium hexanitrorhodate(III) and dichlorodiamminoplatinum under the effect of hexadecyl dimethylamino ethyl sulfate, drying to remove the moisture, firing in a muffle furnace 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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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/652B01J20/20B01J20/30C02F1/78
CPCB01J20/04B01J20/06B01J20/08B01J20/10B01J20/103B01J20/16B01J20/20C02F1/725C02F1/78B01J23/6525B01J37/084B01J37/10C02F2305/02B01J2220/4806B01J2220/42B01J2220/4812B01J35/60
Inventor 朱明夏梦琦石雨晴
Owner SICHUAN NORMAL UNIV