CN1970145A - Catalyst for promoting ozone freeradical yield and its preparation method - Google Patents

Catalyst for promoting ozone freeradical yield and its preparation method Download PDF

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CN1970145A
CN1970145A CNA2005101256054A CN200510125605A CN1970145A CN 1970145 A CN1970145 A CN 1970145A CN A2005101256054 A CNA2005101256054 A CN A2005101256054A CN 200510125605 A CN200510125605 A CN 200510125605A CN 1970145 A CN1970145 A CN 1970145A
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component
catalyst
ozone
sintering
preparation
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刘英慧
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/20Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters

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Abstract

It relates to a catalyst for forming ozone free radicals mixed with Al2O3, CuSO4, TiO2 and metal oxidization, with Al2O3 ingredient 20-40%, CuSO4 10%-20%, TiO2 10%-30%, with the metal oxidization mixture formed by Na(Mg,Fe,Mn,Li,Al)3Al6[Si6O18](BO3)3(OH,F)4 or K(Li,Al)3[(F,OH,O)2|(Si,Al)4O10], with ingredient 20-40%, going through the processes of mixing with ingredients, and sintering to get catalysts. With the function of ultra violet, ultra sonic, electromagnetic wave, electrical field and magnetic filed, it greatly improves the generating quantity of ozone free radicals with improved treatment effects for polluted water and air.

Description

Improve the Catalysts and its preparation method of ozone freeradical yield
Technical field
The present invention relates to a kind of Catalysts and its preparation method that improves ozone freeradical yield, particularly a kind of can be under the effect in electromagnetic wave or ultrasonic wave or electric field or magnetic field, ozone decomposed fast and significantly improve metal oxide catalyst and this Preparation of catalysts method of ozone freeradical yield.
Background technology
As everyone knows, drink contaminated water and can cause the generation of corresponding disease, the water of Wu Raning also can produce direct influence to vegeto-animal growth simultaneously, and the harmful substance in the water can be accumulated in the animal and plant body, and human edible these animals and plants will bring harm to health.In addition, the necessary air-polluting of life increases the weight of equally also threatening human beings'health, with regard to present known human the disease that takes a disease more than 80% with to drink unclean water relevant with the air of edible contaminated food products and aspiration contamination.
Along with people improve day by day to the protection of healthy living, natural environment consciousness, the poisonous and harmful substance of discharging is controlled, cleared up, sewage is administered and the work that air purifies has been obtained the general attention of people.
In high concentration, high harm, in the processing of high toxicity organic sewage, at present oxidizing process that adopt more, its basic principle mainly is to utilize the strong oxidation characteristic of hydroxyl radical free radical, and oxidation Decomposition is difficult to the mode of other biochemical oxidations oxidation processes that organic pollution materials carried out.The method that produces hydroxyl radical free radical is more, and ozone is a kind of method that is commonly used to produce free radical.This province of ozone has strong oxidability, and its oxidation-reduction potential is 2.07V, is only second to fluorine (oxidation-reduction potential is 3.0V) and hydroxyl radical free radical (oxidation-reduction potential is 2.79).Ozone and free radical thereof can the most of organic matters of oxidation, simultaneously to bacterium, microorganism such as fungi and virus also has very strong oxidation, they can directly be had an effect with microorganism, the structure of destroy microorganisms, stop metabolism growth and the breeding of microorganism, cause the dissolving death of microorganism.
Ozone and organic reaction are by two Basic Ways, the one, direct reaction, this reaction is selectively as ozone, the 2nd, indirect reaction, in this reaction, ozone is oxidant with the free radical that decomposition reaction generates, the not only rapid but also non-selectivity of the indirect reaction of these free radical types.Because the oxidation reaction non-selectivity of free radical, they almost can all organic matters of oxidation, are confined to some specific pollutant unlike ozone molecule.Hence one can see that, if decomposition that can accelerate ozone makes it generate a large amount of ozone free radicals, just can the air of the water of pollution and pollution be carried out efficiently, purified treatment completely.
Because the generating mode of ozone free radical normally generates in the decomposable process of above-mentioned ozone, therefore, its formation efficiency is lower, can't satisfy the efficient purification treatment requirement to sewage, air.
Summary of the invention
The objective of the invention is at the efficient of above-mentioned ozone free radical that selective oxidation reaction generates lower, can't satisfy efficient purification treatment requirement to sewage, air, and provide a kind of catalyst and this Preparation of catalysts method thereof that improves ozone freeradical yield, can prepare described catalyst easily by described preparation method, this catalyst can improve the growing amount of free radical under the radiation in ultraviolet ray, ultrasonic wave, electromagnetic wave, electric field, magnetic field, improve sewage and air-polluting governance efficiency.
For achieving the above object, a kind of catalyst that improves ozone freeradical yield of the present invention, this catalyst comprises Al 2O 3, CuSO 4, TiO 2Mixture with metal oxide; Described Al 2O 3Component be 20-40%, be used for carrier as catalyst; Described CuSO 4Component be 10%-20%; Described TiO 2Component be 10%-30%; The mixture of described metal oxide is Na (Mg, Fe, Mn, Li, AL) 3AL 6[Si 6O 18] (BO 3) 3(OH, F) 4Or K (Li, Al) 3[(F, OH, O) 2| (Si, Al) 4O10], the component of the mixture of this metal oxide is 20-40%.
A kind of method for preparing catalyst of the present invention, it may further comprise the steps:
Step 1, will weigh form described catalyst each component mix, obtain compound;
Step 2, described compound is carried out sintering, the temperature value of sintering is 1000 ℃-1200 ℃;
Step 3, with the cooling of the described compound behind the sintering, obtain described catalyst.
As shown from the above technical solution, the present invention will be as the Al of carrier 2O 3With CuSO 4, TiO 2After the high temperature sintering combination, constitute catalyst with the mixture of metal oxide, this catalyst can be under the radiation in ultraviolet ray, ultrasonic wave, electromagnetic wave, electric field, magnetic field, the amount that makes ozone decompose the free radical that generates is greatly improved, when being used for that sewage and contaminated air are carried out governance process, governance efficiency and regulation effect are significantly improved.
Below, also the present invention is described in further detail in conjunction with the accompanying drawings by specific embodiment.
Description of drawings
Figure 1 shows that the flow chart of a preferred embodiment of method for preparing catalyst of the present invention.
The specific embodiment
Catalyst of the present invention comprises Al 2O 3, CuSO 4, TiO 2With the mixture of metal oxide, and through the sintered combination formation.Al 2O 3Be shaped as graininess, shared component is 20-40% in catalyst.Al 2O 3Be used for the carrier as catalyst, its concrete embodiment that forms is as follows:
Embodiment one
Al 2O 3Component is 20-40%
CuSO 4Component is 10%-20%
TiO 2Component is 10%-30%
Na (Mg, Fe, Mn, Li, AL) 3AL 6[Si 6O 18] (BO 3) 3(OH, F) 4Component is 20-40%
The ZnO component is 5%-25%
The AgO component is 2%-8%
Fe 2O 3Component is 10%-30%
Ce elemental constituent is 1%-5%
Embodiment two
Al 2O 3Component is 20-40%
CuSO 4Component is 10%-20%
TiO 2Component is 10%-30%
K (Li, Al) 3[(F, OH, O) 2| (Si, Al) 4O 10] component is 20-40%
The NiO component is 10%-20%
WO 3Component is 10%-30%
MnO 2Component is 3%-6%
The oxide component of Ru is 1%-5%
Among above-mentioned two embodiment, the selecting for use of oxide, interpolation and consumption, can match flexibly at the concrete water of processing or pollution level, major pollutants attribute and the desired degree of treatment of gas of needing, and Ce element that adds or the oxide of Ru, can also substitute with the oxide of the oxide of Nd element or Rh element or Pd element or Pt element or Ce element and Nd element, Rh element, Pd element, Pt element, its objective is in order to improve activity of such catalysts.
A preparation method's of the present invention most preferred embodiment may further comprise the steps:
Each component of step 11, the composition catalyst that will weigh is mixed, and obtains compound;
Step 12, compound is carried out sintering at 1050 ℃, the time of sintering is 4-8 hour, and brings up to 1050 ℃ with constant speed in 1 hour;
Step 13, with the cooling of the described compound behind the sintering, obtain described catalyst.
In above-mentioned preparation process, sintering temperature also can be controlled at 1000 ℃-1200 ℃, and the concrete time can be set according to concrete needs.
It should be noted last that: above embodiment is the unrestricted technical scheme of the present invention in order to explanation only, although the present invention is had been described in detail with reference to the foregoing description, those of ordinary skill in the art is to be understood that: still can make amendment or be equal to replacement the present invention, and not break away from the spirit and scope of the present invention.

Claims (8)

1, a kind of catalyst that improves ozone freeradical yield is characterized in that described catalyst comprises Al 2O 3, CuSO 4, TiO 2Mixture with metal oxide; Described Al 2O 3Component be 20-40%, be used for carrier as catalyst; Described CuSO 4Component be 10%-20%; Described TiO 2Component be 10%-30%; The mixture of described metal oxide is Na (Mg, Fe, Mn, Li, AL) 3AL 6[Si 6O 18] (BO 3) 3(OH, F) 4Or K (Li, Al) 3[(F, OH, O) 2| (Si, Al) 4O10], the component of the mixture of this metal oxide is 20-40%.
2, the catalyst of raising ozone freeradical yield according to claim 1 is characterized in that described Al 2O 3Be graininess.
3, the catalyst of raising ozone freeradical yield according to claim 1 and 2 is characterized in that also comprising in the described catalyst that component is that NiO and/or the component that the ZnO of 5%-25% and/or AgO that component is 2%-8% and/or component are 10%-20% is the WO of 10%-30% 3And/or component is the Fe of 10%-30% 2O 3And/or component is the MnO of 3%-6% 2,
4, the catalyst of raising ozone freeradical yield according to claim 1 and 2, it is characterized in that in the described catalyst also increasing that component is arranged is the Ce element of 1%-5% or the oxide of Nd element or Ru element or Rh element or Pd element or Pt element or described Ce element, Nd element, Ru element, Rh element, Pd element and Pt element, be used to improve described activity of such catalysts.
5, a kind of based on the arbitrary described Preparation of catalysts method of aforesaid right requirement 1-4, it is characterized in that may further comprise the steps:
Each component of step 1, the described catalyst of composition that will weigh is mixed, and obtains compound;
Step 2, described compound is carried out sintering, the temperature value of sintering is 1000 ℃-1200 ℃;
Step 3, with the cooling of the described compound behind the sintering, obtain described catalyst.
6, preparation method according to claim 5 is characterized in that, the sintering time in the described step 2 is 4-8 hour.
7, preparation method according to claim 5 is characterized in that, the sintering temperature in the described step 2 was brought up to 1000 ℃-1200 ℃ with constant speed in 1 hour.
According to claim 5,6 or 7 described preparation methods, it is characterized in that 8, described sintering temperature is 1050 ℃.
CNA2005101256054A 2005-11-24 2005-11-24 Catalyst for promoting ozone freeradical yield and its preparation method Pending CN1970145A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103120922A (en) * 2013-02-06 2013-05-29 浙江工商大学 Gas plasma discharging reactor loaded with salt catalyst and application method
CN104014346A (en) * 2014-05-16 2014-09-03 程帆 Heterogeneous metal catalyst for ozonation enhancement as well as preparation method and application of catalyst
CN111704129A (en) * 2020-07-02 2020-09-25 张德志 Preparation method of graphene oxide
CN114870906A (en) * 2021-02-05 2022-08-09 陕西青朗万城环保科技有限公司 Method and device for generating catalyst
WO2023249571A1 (en) * 2022-06-23 2023-12-28 Ponglikhittanon Apichet Method and system for gas treatment and purification using modified advanced oxidation technology

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103120922A (en) * 2013-02-06 2013-05-29 浙江工商大学 Gas plasma discharging reactor loaded with salt catalyst and application method
CN104014346A (en) * 2014-05-16 2014-09-03 程帆 Heterogeneous metal catalyst for ozonation enhancement as well as preparation method and application of catalyst
CN111704129A (en) * 2020-07-02 2020-09-25 张德志 Preparation method of graphene oxide
CN114870906A (en) * 2021-02-05 2022-08-09 陕西青朗万城环保科技有限公司 Method and device for generating catalyst
WO2023249571A1 (en) * 2022-06-23 2023-12-28 Ponglikhittanon Apichet Method and system for gas treatment and purification using modified advanced oxidation technology

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