CN109304172A - A kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications - Google Patents
A kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications Download PDFInfo
- Publication number
- CN109304172A CN109304172A CN201711133476.2A CN201711133476A CN109304172A CN 109304172 A CN109304172 A CN 109304172A CN 201711133476 A CN201711133476 A CN 201711133476A CN 109304172 A CN109304172 A CN 109304172A
- Authority
- CN
- China
- Prior art keywords
- catalyst
- mesoporous
- high dispersing
- nitrate
- microporous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/66—Silver or gold
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/002—Mixed oxides other than spinels, e.g. perovskite
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/615—100-500 m2/g
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/63—Pore volume
- B01J35/633—Pore volume less than 0.5 ml/g
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/64—Pore diameter
- B01J35/647—2-50 nm
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/06—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases
- F23G7/07—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases in which combustion takes place in the presence of catalytic material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Catalysts (AREA)
Abstract
The invention discloses a kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications, belong to petrochemical industry.Which solve precious metal catalyst combustion catalyst load capacity existing in VOCs catalytic combustion process is low, cause effectively to contact in reaction process it is poor, while the defects of noble metal catalyst is at high cost, sulfur resistive is not malicious.The present invention is using silver nitrate and aluminium isopropoxide as raw material, transition metal nitrate is auxiliary agent, and P123 is template, introduces hydrochloric acid, nitric acid or phosphoric acid and adjusts acid-base property, synthetic reaction is carried out by " solvent volatilization-solute self assembly " method, the mesoporous Ag-Al catalyst being finally prepared by roasting.The Ag-Al catalyst that the present invention is prepared has high reactivity to waste gas containing benzene, is 35000h in air speed‑1Under conditions of, reaction temperature is lower than 280 DEG C when conversion ratio is not less than 99%, and alternative noble metal catalyst is in catalytic combustion process.
Description
Technical field
The invention belongs to petrochemical industry, it is related to a kind of volatile organic compounds catalyst for catalytic combustion and its preparation
Method, especially a kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications.
Background technique
With China start to push forward comprehensively implementation " petroleum refining industry pollutant emission standard " (GB31570-2015) and
" petro chemical industry pollutant emission standard " (GB31571-2015), volatile organic compounds (VOCs) and Partial Feature are dirty
The discharge needs of dye object reach harsher requirement.Required in above-mentioned two standard the treatment effeciency of non-methane total hydrocarbons >=
97%, non-methane hydrocarbon emission limit value≤120mg/m3, benzene≤4mg/m is required in organic properties pollutant emission limit3, toluene
≤15mg/m3, dimethylbenzene≤20mg/m3.Traditional oil-gas recovery method, including absorption method, absorption process, membrane separation process, condensation method
And combinations thereof technique, such as absorption-absorption process, condensation-absorption method be difficult to reach so low emission request.Therefore, it is catalyzed
The popularization and application of burning process are extremely urgent tasks.
Currently, being directed to the catalytic combustion process of VOCs, what industrially application was more is noble metal catalyst, such as platinum group, palladium
Series catalysts.The advantages of noble metal catalyst is that its catalytic reaction activity is higher, and initiation temperature is lower.But due to noble metal
Very rare, price is very expensive, and leading to entire catalytic combustion system, the cost is relatively high, answers to limit its popularization
With.Meanwhile common noble metal catalyst is prepared using infusion process, is limited to the low-down load capacity of active component, usually
No more than 0.5wt.%, cause on carrier (such as γ-Al2O3Or SiO2) overwhelming majority that exposes is non-catalytic reaction activity
Carrier surface, be unfavorable for effectively contacting and subsequent reaction between reaction raw materials and catalyst activity component, thus seriously
Affect catalytic reaction activity.In addition, being produced for refinery, oil depot etc. in discharged VOCs, it will usually containing having for some
Machine sulfide, and noble metal catalyst is very easy to sulfur poisoning and leads to not play reactivity.
Summary of the invention
In order to solve above-mentioned defect existing in the prior art, the present invention passes through " solvent volatilization-solute self assembly " method
It is prepared for a kind of mesoporous Ag-Al catalyst of active component high degree of dispersion, alternative noble metal catalyst is for being catalyzed burner
Skill.
One of task of the invention is to provide a kind of high dispersing microporous/mesoporous Ag-Al catalyst.
A kind of high dispersing microporous/mesoporous Ag-Al catalyst, required raw material include catalyst activity component, auxiliary agent, catalyst carrier,
Template and solvent;
The catalyst activity component is selected from silver nitrate, and the auxiliary agent is nitrate;
The catalyst carrier is aluminium isopropoxide, and the template is selected from polyethylene oxide-polypropylene oxide-polycyclic oxygen second
Alkane triblock copolymer, the solvent are Organic Alcohol;
The mass content of Ag is 1~30% in the Ag-Al catalyst, and the mass content of the auxiliary agent is 0.1~20%,
The specific surface area of the Ag-Al catalyst is 250~400m2/g。
The direct bring advantageous effects of above-mentioned technical proposal are as follows:
Active component A g and auxiliary agent are anchored in mesopore orbit, not only facilitate the high degree of dispersion of active component, while solely
The interaction of special mesopore orbit structure feature and active component and mesopore orbit wall aluminium oxide can be reasonably resistant to organic sulfur
Poisoning effect of the compound to active component.Meanwhile high dispersing microporous/mesoporous Ag-Al catalyst specific surface area with higher and relatively narrow
Pore distribution enhances reaction raw materials in the diffusion of catalyst, promotes catalyst reaction activity.
As a preferred solution of the present invention, the nitrate solution is selected from cerous nitrate, lanthanum nitrate, manganese nitrate, nitric acid
The mixture of one or both of cobalt or zirconium nitrate.
As another preferred embodiment of the invention, the organic alcohol solvent is selected from methanol, ethyl alcohol, 1- propyl alcohol or 2- third
Alcohol.
Another task of the invention is to provide the preparation method of above-mentioned high dispersing microporous/mesoporous Ag-Al catalyst, successively includes
Following steps:
A weighs a certain amount of template and aluminium isopropoxide respectively, measures a certain amount of acid, is added sequentially to stir in container
Until dissolution;
B weighs a certain amount of silver nitrate solution and auxiliary agent is added in the container of step a, and stirs;
Step b is equipped with the container closure of silver nitrate solution and auxiliary agent by c, is stirred at room temperature;
After d opens vessel port, it is placed in baking oven and controls in 50~70 DEG C of dry no less than 12h;
E takes out the solid after drying in an oven, then is roasted up to high dispersing microporous/mesoporous Ag-Al catalyst.
Further, the additional amount of the template and the quality proportioning of aluminium isopropoxide are 0.1~0.7:1.
Further, above-mentioned roasting process carries out in Muffle furnace, with 1~2 DEG C/min of heating rate in roasting process
It is warming up to 500 DEG C and maintains 4 hours, and Muffle furnace air is in displacement circulation status.
Further, above-mentioned acid is hydrochloric acid, nitric acid or phosphoric acid, above-mentioned acid and the quality proportioning of aluminium isopropoxide be 0.3~
1:1。
In above-mentioned preparation method, committed step is to adjust content, assistant types and the content of active component silver and above-mentioned
The type and dosage of acid, the adjusting of mixing time and calcination procedure is added in the material ratio of the two and aluminium isopropoxide, and roasts
Program includes the parameters such as heating rate, platform temperature, maturing temperature again.By the adjusting of above-mentioned key parameter, can effectively adjust
Control the physical-chemical parameters such as the active composition of high dispersing microporous/mesoporous Ag-Al catalyst, surface topography, microstructure, pore property.
Another task of the invention is to provide application of the above-mentioned Ag-Al catalyst in catalytic combustion process.
Above-mentioned concrete application is embodied in: in catalytic combustion process, being handled the organic sulfur compound in VOCs.
Compared with prior art, high dispersing microporous/mesoporous Ag-Al method for preparing catalyst proposed by the present invention is novel, the object of product
Physicochemical nature parameters are easy to regulate and control, catalytic reaction activity and sulfur resistive poison better performances, while may be implemented extensive in factory
Metaplasia produces, and facilitates product and prepares conversion to industrial application from laboratory.
Compared with existing loaded noble metal catalyst, the Ag-Al catalyst used in the present invention is using novel
" solvent volatilization-solute self assembly " method is prepared, and active component can be highly dispersed in catalyst duct, to play
Higher reactivity;Meanwhile active component silver and auxiliary agent are anchored in mesopore orbit, it is mutual between cell walls aluminium oxide
Effect can effectively resist the poisoning effect of organic sulfur compound;Finally, novel is high dispersing microporous/mesoporous compared with noble metal catalyst
Ag-Al catalyst cost has to be declined more significantly, has more wide prospects for commercial application and economic benefit.
Ag-Al catalyst specific surface area with higher, reaches 250m prepared by the present invention2/ g or more, unique Jie
Hole pore distribution enhances the haptoreaction between VOCs and active component, lower to the initiation temperature of benzene, reaches 250 DEG C, complete
Full conversion temperature (conversion ratio >=99%) is not higher than 280 DEG C.Active component and the interaction of mesopore orbit wall inhibit simultaneously
Toxic action of the sulfide to catalyst.Therefore, the Ag-Al catalyst is in the zero-emission field that becomes of VOCs with wide application
Prospect and commercial value.
Detailed description of the invention
The present invention will be further described with reference to the accompanying drawing:
Fig. 1 is the high dispersing microporous/mesoporous Ag-Al catalyst electron scanning micrograph of the present invention;
Fig. 2 is the low temperature nitrogen adsorption desorption curve graph of high dispersing microporous/mesoporous Ag-Al catalyst;
Fig. 3 is high dispersing microporous/mesoporous Ag-Al catalyst graph of pore diameter distribution.
Specific embodiment
It is of the invention in order to make the invention proposes a kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications
Advantage, technical solution are clearer, clear, elaborate combined with specific embodiments below to the present invention.
Raw material needed for the present invention can be commercially available by commercial channel,
Template used dose of polyethylene oxide-polypropylene oxide-polyethylene oxide triblock copolymer of the invention, it is real below
It applies and is referred to as P123 in example.
Embodiment 1:
In the present embodiment, being prepared for the Ag-Al catalyst that the mass ratio of Ag:Ce:Al is about 10:2:88, (Ce is to help
Agent).
It is specific the preparation method is as follows:
Firstly, 21g template P123 is dissolved in the beaker for filling 400mL1- propyl alcohol, 32mL concentrated nitric acid and 41g are added
Aluminium isopropoxide is continuously vigorously stirred 30 minutes;
Secondly, by 6.8g silver nitrate (AgNO3) and 1.2g cerous nitrate (Ce (NO3)3·6H2O it) is sequentially added in above-mentioned solution
And it is stirred continuously;
Then, beaker mouth is covered with PET plastic film and bound, continuously stir 12 hours;
PET plastic film is removed, and is placed the beaker in vacuum oven, it is 14 hours dry at 55 DEG C;
Finally, the plastic-like solid in beaker is taken out, it is placed in Muffle furnace, is warming up to 2 DEG C/min of heating rate
500 DEG C and maintenance 4 hours, during which Muffle furnace air is constantly in displacement circulation status.It takes out when being down to room temperature to get height
Disperse mesoporous Ag-Al catalyst.
The mass ratio of each component Ag:Ce:Al is about 10:2:88 in catalyst manufactured in the present embodiment (in terms of oxide).
Electron microscope analysis and performance test are done to the high dispersing microporous/mesoporous Ag-Al catalyst that the present embodiment is prepared.Electronic Speculum point
As shown in FIG. 1, FIG. 1 is the scanning electron microscope (SEM) of high dispersing microporous/mesoporous Ag-Al catalyst characterization, Fig. 1 shows by new for analysis
In the Ag-Al catalyst of " solvent volatilization-solute self assembly " the method preparation of type, active component is gathered in one in a manner of piling up
It rises.
Fig. 2 is the low temperature nitrogen adsorption desorption curve of high dispersing microporous/mesoporous Ag-Al catalyst, and display Ag-Al catalyst has allusion quotation
The Type IV type of type shows that the Ag-Al catalyst has mesopore orbit feature, while its BET method specific surface area reaches
325m2/ g, Kong Rong have also reached 0.47cm3/g;
Fig. 3 is the graph of pore diameter distribution of high dispersing microporous/mesoporous Ag-Al catalyst, display product pore-size distribution is concentrated mainly on 1~
Between 8nm, most probable pore size is 6nm or so.
Embodiment 2:
In the present embodiment, being prepared for the Ag-Al catalyst that the mass ratio of Ag:La:Al is about 20:5:75, (La is to help
Agent).
Specific preparation method the following steps are included:
Firstly, 12g template P123 is dissolved in the beaker for filling 400mL methanol, adds 21mL concentrated hydrochloric acid and 27g is different
Aluminium propoxide is continuously vigorously stirred 30 minutes;
Secondly, by 5.3g silver nitrate (AgNO3) and 2.4g lanthanum nitrate (La (NO3)3·6H2O it) is sequentially added in above-mentioned solution
And it is stirred continuously;
Then, beaker mouth is covered with PET plastic film and bound, continuously stir 12 hours;
PET plastic film is removed, and is placed the beaker in vacuum oven, it is 16 hours dry at 55 DEG C;
Finally, the plastic-like solid in beaker is taken out, it is placed in Muffle furnace, is warming up to 2 DEG C/min of heating rate
500 DEG C and maintenance 4 hours, during which Muffle furnace air is constantly in displacement circulation status.It takes out when being down to room temperature to get height
Disperse mesoporous Ag-Al catalyst.
The mass ratio of each component Ag:La:Al is about 20:5:75 in catalyst manufactured in the present embodiment (in terms of oxide).
Pass through the Ag-La-Al catalyst of this kind of novel " solvent volatilization-solute self assembly " method preparation, the SEM result of gained sample
It is similar with Fig. 1 result, it was demonstrated that the Ag-Al catalyst series with similar microstructure can be prepared by this kind of method.
Low temperature nitrogen adsorption desorption the experimental results showed that, improve the content of active component and introduced after auxiliary agent lanthanum simultaneously, BET
There is a little decline in specific surface area, is 295m2/ g, Kong Rong have been also reduced to 0.42cm3/ g, and its Type IV type meso pore characteristics
No change has taken place.
Embodiment 3:
In the present embodiment, the Ag-Al catalyst (not adding auxiliary agent) that the mass ratio for being prepared for Ag:Al is about 25:75.
Specific preparation method the following steps are included:
Firstly, 18g template P123 is dissolved in the beaker for filling 400mL dehydrated alcohol, add 28mL concentrated nitric acid and
23g aluminium isopropoxide is continuously vigorously stirred 30 minutes;
Secondly, by 5.6g silver nitrate (AgNO3) be sequentially added in above-mentioned solution and be stirred continuously;
Then, beaker mouth is covered with PET plastic film and bound, continuously stir 16 hours;
PET plastic film is removed, and is placed the beaker in vacuum oven, it is 15 hours dry at 65 DEG C;
Finally, the plastic-like solid in beaker is taken out, it is placed in Muffle furnace, is heated up with 1.5 DEG C/min of heating rate
It to 500 DEG C and maintains 5 hours, during which Muffle furnace air is constantly in displacement circulation status.Taking-up when being down to room temperature, obtains
High dispersing microporous/mesoporous Ag-Al catalyst,
The mass ratio of each component Ag:Al is about 25:75 in the catalyst (in terms of oxide).
Using waste gas containing benzene as raw material, the reactivity of catalyst in embodiment 1,2 and 3 is investigated, as shown in table 1.
Note: reaction velocity 35000h-1。
Embodiment 4:
In the present embodiment, be prepared for Ag-Al catalyst that the mass ratio of Ag:Ce:La:Al is about 15:5:5:75 (Ce,
La is auxiliary agent).
Specific preparation method the following steps are included:
Firstly, 32g template P123 is dissolved in the beaker for filling 400mL methanol, 42mL phosphoric acid and 49g isopropyl are added
Aluminium alcoholates is continuously vigorously stirred 30 minutes;
Secondly, by 9.6g silver nitrate (AgNO3), 2.0g cerous nitrate (Ce (NO3)3·6H2) and 2.2g lanthanum nitrate (La O
(NO3)3·6H2O it) is sequentially added in above-mentioned solution and is stirred continuously;
Then, beaker mouth is covered with PET plastic film and bound, continuously stir 18 hours;
PET plastic film is removed, and is placed the beaker in vacuum oven, it is 12 hours dry at 70 DEG C;
Finally, the plastic-like solid in beaker is taken out, it is placed in Muffle furnace, is warming up to 1 DEG C/min of heating rate
500 DEG C and maintenance 4 hours, during which Muffle furnace air is constantly in displacement circulation status.Taking-up when being down to room temperature, obtains height
Disperse mesoporous Ag-Al catalyst,
The mass ratio of each component Ag:Ce:La:Al is about 15:5:5:75 (with oxide in catalyst manufactured in the present embodiment
Meter).
Auxiliary agent selected by the present invention is cerous nitrate (Ce (NO3)3·6H2O), lanthanum nitrate (La (NO3)3·6H2O), manganese nitrate (Mn
(NO3)2), cobalt nitrate (Co (NO3)2·6H2O), zirconium nitrate (Zr (NO3)4·5H2O), under the guide of above-described embodiment 1-4,
Its unlisted auxiliary agent embodiment and combinations thereof can be realized obviously.
In addition, above-described embodiment 1-4 is not limitation of the invention, in the actual production process, technological parameter and
Proportion can be met needed for production by multiple amplification.
It should be understood that any equivalent way that those skilled in the art are made under the introduction of this specification, or
Obvious variant should all be within the scope of the present invention.
Claims (9)
1. a kind of high dispersing microporous/mesoporous Ag-Al catalyst, it is characterised in that: required raw material includes catalyst activity component, auxiliary agent, urges
Agent carrier, template and solvent;
The catalyst activity component is selected from silver nitrate, and the auxiliary agent is nitrate;
The catalyst carrier is aluminium isopropoxide, and the template is selected from polyethylene oxide-polypropylene oxide-polyethylene oxide three
Block copolymer, the solvent are Organic Alcohol;
The mass content of Ag is 1~30% in the Ag-Al catalyst, and the mass content of the auxiliary agent is 0.1~20%, described
The specific surface area of Ag-Al catalyst is 250~400m2/g。
2. high dispersing microporous/mesoporous Ag-Al catalyst according to claim 1, it is characterised in that: the nitrate solution is selected from
The mixture of one or both of cerous nitrate, lanthanum nitrate, manganese nitrate, cobalt nitrate or zirconium nitrate.
3. high dispersing microporous/mesoporous Ag-Al catalyst according to claim 1, it is characterised in that: the solvent Organic Alcohol is selected from
Ethyl alcohol, methanol, 1- propyl alcohol or 2- propyl alcohol.
4. the preparation method of high dispersing microporous/mesoporous Ag-Al catalyst according to claim 1, which is characterized in that successively include
Following steps:
A weighs a certain amount of template and aluminium isopropoxide respectively, measures a certain amount of acid, be added sequentially in container stirring until
Dissolution;
B weighs a certain amount of silver nitrate solution and auxiliary agent is added in the container of step a, and stirs;
Step b is equipped with the container closure of silver nitrate solution and auxiliary agent by c, is stirred at room temperature;
After d opens vessel port, it is placed in baking oven controlled at 50~70 DEG C of dry no less than 12h;
E takes out the solid after drying in an oven, then is roasted up to high dispersing microporous/mesoporous Ag-Al catalyst.
5. the preparation method of high dispersing microporous/mesoporous Ag-Al catalyst according to claim 4, it is characterised in that: the template
The quality proportioning of the additional amount aluminium isopropoxide of agent is 0.1~0.7:1.
6. the preparation method of high dispersing microporous/mesoporous Ag-Al catalyst according to claim 4, it is characterised in that: roasting process
It carries out, be warming up to 500 DEG C in the roasting process with 1~2 DEG C/min of heating rate and maintain 4 hours in Muffle furnace, and
Muffle furnace air is in displacement circulation status.
7. the preparation method of high dispersing microporous/mesoporous Ag-Al catalyst according to claim 4, it is characterised in that: in step c
12~18h is stirred at room temperature.
8. the preparation method of high dispersing microporous/mesoporous Ag-Al catalyst according to claim 4, it is characterised in that: the acid
For hydrochloric acid, nitric acid or phosphoric acid, the quality proportioning of the acid and aluminium isopropoxide is 0.3~1:1.
9. application of the high dispersing microporous/mesoporous Ag-Al catalyst according to claim 1 in catalytic combustion process.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201711133476.2A CN109304172A (en) | 2017-11-16 | 2017-11-16 | A kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201711133476.2A CN109304172A (en) | 2017-11-16 | 2017-11-16 | A kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications |
Publications (1)
Publication Number | Publication Date |
---|---|
CN109304172A true CN109304172A (en) | 2019-02-05 |
Family
ID=65205410
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201711133476.2A Pending CN109304172A (en) | 2017-11-16 | 2017-11-16 | A kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109304172A (en) |
Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7211238B2 (en) * | 2003-03-12 | 2007-05-01 | Abb Lummus Global Inc. | Mesoporous aluminum oxide, preparation and use thereof |
CN101992105A (en) * | 2010-11-12 | 2011-03-30 | 大连理工大学 | Sliver-based bimetallic catalyst for catalyzing oxidation of volatile organic contaminant, preparation method and application thereof |
CN102240570A (en) * | 2010-05-11 | 2011-11-16 | 北京化工大学 | Catalyst with meso pore characteristics and application thereof |
CN102441375A (en) * | 2011-11-03 | 2012-05-09 | 华东理工大学 | Homogeneous mesoporous rhodium oxide / alumina composite catalysis material, preparation method and application thereof |
CN103157491A (en) * | 2011-12-12 | 2013-06-19 | 中国科学院生态环境研究中心 | Mesoporous metal oxide-supported palladium catalyst used for catalytic oxidation of volatile organic compounds |
CN103203233A (en) * | 2013-05-03 | 2013-07-17 | 云南大学 | Palladium-based catalyst for methane catalytic combustion and preparation of palladium-based catalyst |
CN103285865A (en) * | 2012-02-23 | 2013-09-11 | 南京工程学院 | Catalyst for synthesizing benzaldehyde by carrying out liquid-phase high-selectivity catalytic oxidation on methylbenzene |
CN103303903A (en) * | 2013-06-09 | 2013-09-18 | 中国检验检疫科学研究院 | Metal or metal oxide loaded mesoporous carbon material and preparation method thereof |
CN104138756A (en) * | 2014-08-02 | 2014-11-12 | 孙超 | Supported catalyzer for low-temperature catalytic combustion of VOCs and method for preparing supported catalyzer for low-temperature catalytic combustion of VOCs |
CN104148040A (en) * | 2014-07-24 | 2014-11-19 | 华东师范大学 | Aluminum matrix-mesoporous alumina composite material and preparation method and application of aluminum matrix-mesoporous alumina composite material |
CN104588020A (en) * | 2014-12-17 | 2015-05-06 | 中国人民解放军防化学院 | Preparation method of ordered mesoporous alumina supported metal catalyst |
CN104923215A (en) * | 2015-05-07 | 2015-09-23 | 中国石油大学(北京) | Precious-metal-supported ordered mesoporous alumina material, and synthetic method and application thereof |
CN105618061A (en) * | 2016-01-29 | 2016-06-01 | 太原理工大学 | Slurry bed carbon dioxide methanation bimetallic catalyst and preparation method and application thereof |
CN106732552A (en) * | 2016-11-04 | 2017-05-31 | 昆明贵研催化剂有限责任公司 | A kind of meso-porous alumina loads the preparation method and applications of palladium-based catalyst |
CN107096527A (en) * | 2017-05-22 | 2017-08-29 | 西安石油大学 | A kind of normal-temperature efficient catalysis oxidation formaldehyde catalyst, preparation method and application |
CN107398295A (en) * | 2017-08-03 | 2017-11-28 | 江西国君环保科技有限公司 | A kind of catalyst and preparation method for catalytic purification VOC |
-
2017
- 2017-11-16 CN CN201711133476.2A patent/CN109304172A/en active Pending
Patent Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7211238B2 (en) * | 2003-03-12 | 2007-05-01 | Abb Lummus Global Inc. | Mesoporous aluminum oxide, preparation and use thereof |
CN102240570A (en) * | 2010-05-11 | 2011-11-16 | 北京化工大学 | Catalyst with meso pore characteristics and application thereof |
CN101992105A (en) * | 2010-11-12 | 2011-03-30 | 大连理工大学 | Sliver-based bimetallic catalyst for catalyzing oxidation of volatile organic contaminant, preparation method and application thereof |
CN102441375A (en) * | 2011-11-03 | 2012-05-09 | 华东理工大学 | Homogeneous mesoporous rhodium oxide / alumina composite catalysis material, preparation method and application thereof |
CN103157491A (en) * | 2011-12-12 | 2013-06-19 | 中国科学院生态环境研究中心 | Mesoporous metal oxide-supported palladium catalyst used for catalytic oxidation of volatile organic compounds |
CN103285865A (en) * | 2012-02-23 | 2013-09-11 | 南京工程学院 | Catalyst for synthesizing benzaldehyde by carrying out liquid-phase high-selectivity catalytic oxidation on methylbenzene |
CN103203233A (en) * | 2013-05-03 | 2013-07-17 | 云南大学 | Palladium-based catalyst for methane catalytic combustion and preparation of palladium-based catalyst |
CN103303903A (en) * | 2013-06-09 | 2013-09-18 | 中国检验检疫科学研究院 | Metal or metal oxide loaded mesoporous carbon material and preparation method thereof |
CN104148040A (en) * | 2014-07-24 | 2014-11-19 | 华东师范大学 | Aluminum matrix-mesoporous alumina composite material and preparation method and application of aluminum matrix-mesoporous alumina composite material |
CN104138756A (en) * | 2014-08-02 | 2014-11-12 | 孙超 | Supported catalyzer for low-temperature catalytic combustion of VOCs and method for preparing supported catalyzer for low-temperature catalytic combustion of VOCs |
CN104588020A (en) * | 2014-12-17 | 2015-05-06 | 中国人民解放军防化学院 | Preparation method of ordered mesoporous alumina supported metal catalyst |
CN104923215A (en) * | 2015-05-07 | 2015-09-23 | 中国石油大学(北京) | Precious-metal-supported ordered mesoporous alumina material, and synthetic method and application thereof |
CN105618061A (en) * | 2016-01-29 | 2016-06-01 | 太原理工大学 | Slurry bed carbon dioxide methanation bimetallic catalyst and preparation method and application thereof |
CN106732552A (en) * | 2016-11-04 | 2017-05-31 | 昆明贵研催化剂有限责任公司 | A kind of meso-porous alumina loads the preparation method and applications of palladium-based catalyst |
CN107096527A (en) * | 2017-05-22 | 2017-08-29 | 西安石油大学 | A kind of normal-temperature efficient catalysis oxidation formaldehyde catalyst, preparation method and application |
CN107398295A (en) * | 2017-08-03 | 2017-11-28 | 江西国君环保科技有限公司 | A kind of catalyst and preparation method for catalytic purification VOC |
Non-Patent Citations (2)
Title |
---|
GONZALEZ P V ET AL.: ""Thermally Stable Mesoporous Alumina Synthesized with Non-Ionic"", 《MICROPOROUS MESOPOROUS》 * |
贾忱等: ""介孔氧化铝的合成及其催化乙醇脱水的性能"", 《石油化工》 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Masui et al. | Total oxidation of toluene on Pt/CeO2–ZrO2–Bi2O3/γ-Al2O3 catalysts prepared in the presence of polyvinyl pyrrolidone | |
Overbury et al. | XANES Studies of the Reduction Behavior of (Ce 1-y Zr y) O 2 and Rh/(Ce 1-y Zr y) O 2 | |
Parlett et al. | Mesoporous Silicas as Versatile Supports to Tune the Palladium‐Catalyzed Selective Aerobic Oxidation of Allylic Alcohols | |
Ge et al. | Performance study of modified Pt catalysts for the complete oxidation of acetone | |
US20050176580A1 (en) | Catalyst for partial oxidation of hydrocarbon, process for producing the same, process for producing hydrogen-containing gas with the use of the catalyst and method of using hydrogen-containing gas produced with the use of the catalyst | |
CN105797767B (en) | A kind of diesel vehicle oxidation catalyst with low temperature active and preparation method thereof | |
CN110064399A (en) | The preparation of core-shell structure coated with silica cobaltosic oxide catalyst for propane improvement and product and application | |
Cao et al. | Improved activity and durability of Rh-based three-way catalyst under diverse aging atmospheres by ZrO2 support | |
CN100522349C (en) | Novel gamma aluminium oxide catalyst and producing technology | |
CN109225216B (en) | Anti-aging catalyst for purifying volatile organic compounds and preparation method thereof | |
Wang et al. | In situ confinement of PdO within zeolite as robust adsorbent/catalyst for toluene elimination | |
CN109304172A (en) | A kind of high dispersing microporous/mesoporous Ag-Al catalyst, preparation method and applications | |
Vergunst et al. | Carbon coating of ceramic monolithic substrates | |
CN114258322A (en) | Methane oxidation catalyst and methods of making and using same | |
CN101443119A (en) | Sulfur resistant emissions catalyst | |
Xu et al. | Mechanistic understanding of oxygen spillover enables efficient propane combustion over Pt/AlSOx catalyst | |
CN101116821A (en) | Non-uniform combustion catalyst and uses thereof | |
Banus et al. | Structured catalyst for the catalytic combustion of soot: Co, Ba, K/ZrO2 supported on Al2O3 foam | |
CN107345161A (en) | A kind of method for hydrogen cracking of coal tar | |
CN111375423A (en) | High-temperature catalytic combustion catalyst and preparation method thereof | |
CN105688904A (en) | Method for preparing toluene catalytic combustion monolithic catalysts and application | |
Benard et al. | Comparing monolithic and membrane reactors in catalytic oxidation of propene and toluene in excess of oxygen | |
Liao et al. | Preparation of Pd/(Ce1− xYx) O2/γ-Al2O3/cordierite catalysts and its catalytic combustion activity for methane | |
JP4298071B2 (en) | Exhaust gas purification material and method for producing the same | |
Zhou et al. | Enhanced hydrophobic microporous Pt/silica with high adsorption and catalytic oxidation for trace toluene removal |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |