CN1431051A - Visible light catalyst with molecular sieve of silica-alumina media poves as substrate and its preparing method - Google Patents
Visible light catalyst with molecular sieve of silica-alumina media poves as substrate and its preparing method Download PDFInfo
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- CN1431051A CN1431051A CN 03117252 CN03117252A CN1431051A CN 1431051 A CN1431051 A CN 1431051A CN 03117252 CN03117252 CN 03117252 CN 03117252 A CN03117252 A CN 03117252A CN 1431051 A CN1431051 A CN 1431051A
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Abstract
A visual light catalyst based on metaporous Si-Al molecular sieve for removing aldehyde from air is prepared from the metaporous Si-Al molecular sieves MCM-41 and AlMCM-41 and AlMCM-41 and transition metal. The ratio of Si, Al and transition metal is 55-95%; 1-10%:0.1-1 %. Its advantage is high activity.
Description
Affiliated field
The present invention relates to photocatalysis and material chemistry technical field, especially a kind of is the visible light catalyst and preparation method thereof of matrix with the sial mesopore molecular sieve.
Background technology
Along with the enhancing of people's environmental consciousness, the material that exploitation can combine with the Nature resource, or green product have become a main trend to reduce the degree of environmental disruption and to promote quality of the life.In this numerous material, photochemical catalyst is important developing direction wherein.
After the research of the 1970's, first piece of relevant photochemical catalyst was delivered, the researcher of countries in the world dropped into this field one after another.To after nineteen ninety develops relevant commercial product for Japan, photochemical catalyst exploitation and the agitation of using have more been started.In these researchs because titanium dioxide has powerful redox ability, high chemical stability and nontoxic characteristic, thereby photocatalysis research is again the center of gravity of research with the titanic oxide material.Now from the clean requirement of life at home, and even to prevention and control of air pollution, the antibiotic demand of removing practical uses such as mould, fwaater resources protection, all make light-catalysed application enlarge day by day, commercialization speed is accelerated greatly at united states, japan and other countries after 97 years.
Yet, must use special light sources just to produce effect based on the first generation photochemical catalyst of titanium dioxide less than the ultraviolet light of 390nm, almost sharp have more than is neededly have only about 3% to be the sunshine of ultraviolet light.Therefore it is very important and urgent developing responsive to visible light type second generation photochemical catalyst.Because without the special installation of ultraviolet light, sunshine gets final product, so the range of application of visible light catalyst is more more extensive than ultraviolet light catalyst, united states, japan and other countries all rests on development at present.Method commonly used is to go modifying titanium dioxide to reach the purpose that absorbs visible light with transition metal, as number of patent application 01113065.2, name is called the Chinese patent of " preparation method of visual light reaction type nm TiO 2-base optical catalyst ", this patent is just used doped with metal elements titanium dioxide, but does not have carrier.Also the ion beam apparatus of useful costliness removes modifying titanium dioxide with nitrogen, sees R.Asahi, TMorikawa, T.Ohwaki, K.Aoki, and Y.Taga, Science, 2001,293,269-271.But the used light source of the document still has tangible ultraviolet light, and also there is a big difference from practice.
Chinese patent 0115865.4 discloses a kind of name and has been called " visible light responsing type photochemical catalyst ", and this patent is the mixed layer with titanium dioxide and silica, but does not use doped with metal elements.According to applicant's research, there is not mesoporous material to make carrier, there is not containing transition metal yet, visible light catalysis activity is extremely low.
Summary of the invention
It is visible light catalyst of matrix and preparation method thereof that the present invention proposes with the sial mesopore molecular sieve, it adopts transition metal, visible light catalyst as modifications such as Co, and find under visible light the best ultraviolet light catalyst Degussa P25 of effect that can produce with Germany first, active suitable ultraviolet light under to the activity of acetaldehyde degradation reaction.
Purpose of the present invention realizes by following technical measures: with sial mesopore molecular sieve MCM-41 and AlMCM-41 is matrix, it is characterized in that: be doped with transition metal, according to silicon: aluminium: transition metal=55-95%: 1-10%: 0.1-1%, supported titanium dioxide or not supported titanium dioxide all can.
The specific area of above-mentioned visible light catalyst is at 500-1000m
2Between/the g, pore volume is at 0.4-0.8cm
3Between/the g, average pore diameter is between 2.2-3.3nm.
Transition metal in the above-mentioned visible light catalyst includes manganese, iron, chromium, cobalt, nickel, vanadium, tungsten.
Above-mentioned visible light catalyst and the MCM-41 aperture similar with the AlMCM-41 matrix is at other mesoporous material of 2-10nm, and as MCM-48, HMS, the TiMCM-41 material also can be used as matrix.
A kind of preparation method of as above-mentioned visible light catalyst is characterized in that: a. softex kw and dissolution of sodium hydroxide in deionized water; B. in a, add tetraethoxysilance; The soluble-salt of transition metal that c. will be to be mixed dissolves in the appropriate amount of deionized water by solubility, waits to dissolve the back and adds among a; D. with above-mentioned mixed liquor in reactor in 90-120 ℃ of crystallization 5-7 days, filter, washing is dried; E. dry thing is calcined in 500-600 ℃ of air atmosphere and promptly obtained not that supported titanium dioxide is the visible light catalyst of matrix with MCM-41 in 6 hours; F. alchlor is water-soluble and add among a, repeat b-e, promptly obtaining not, supported titanium dioxide is the visible light catalyst of matrix with AlMCM-41; G. with e or f gained sample dispersion in the pure isopropyl alcohol of reagent, add titanium isopropoxide thereupon, be stirred to dried; H. dry thing being calcined in 400-500 ℃ of air atmosphere and promptly being obtained supported titanium dioxide in 3 hours is the visible light catalyst of matrix with MCM-41 or AlMCM-41.
The above-mentioned soluble-salt that is used to prepare visible light catalyst includes villaumite, nitrate, acetate.
Description of drawings:
Fig. 1 be Degussa P25 under visible light (＞420nm), the product carbon dioxide is with the change curve of light application time.
Fig. 2 is that (300nm＜λ＜410nm), acetaldehyde and product carbon dioxide are with the change curve of light application time under ultraviolet light for Degussa P25.
Fig. 3 is the X-ray diffractogram of the prepared visible light catalyst of the present invention.
Fig. 4 is the nitrogen adsorption isotherm figure of the prepared visible light catalyst of the present invention, and solid line is the absorption line, and dotted line is the desorption line.Fig. 3,4 show the mesoporous characteristic of prepared visible light catalyst.
Fig. 5 is the ultraviolet-visible of the prepared visible light catalyst of the present invention spectrogram that diffuses, and shows that prepared visible light catalyst has absorption in visible-range.
Fig. 6 is one of the prepared visible light catalyst of the present invention TiO
2/ Co-MCM-41 under visible light (＞420nm), acetaldehyde and product carbon dioxide are with the change curve of light application time.
Fig. 7 be one of the prepared visible light catalyst of the present invention Co-MCM-41 under visible light (＞420nm), acetaldehyde and product carbon dioxide are with the change curve of light application time.
Photocatalytic activity evaluation method provided by the invention
The model reaction that the acetaldehyde degradation reaction is estimated as photocatalytic activity in the air.The 1000W high-pressure sodium lamp is as light source, and catalyst amount is about 0.15 gram.When carrying out the visible light catalytic experiment, remove to guarantee to filter ultraviolet light with two tablet filters, a slice is for filtering the interference filter below the 400nm, and another sheet is for allowing the coloured glass filter that passes through more than the 420nm.Under such condition, use typical ultraviolet light catalyst, P25 does not have any activity as photochemical catalyst, sees Fig. 1, thereby has proved conclusively and do not have ultraviolet light to pass through.Carrying out ultraviolet catalytic when experiment, the interference filter that can allow 300nm＜λ＜410nm pass through with a slice.This wave band is comparatively typical ultraviolet light range.Go to detect acetaldehyde concentration and product with look-matter coupling, carbon dioxide is with the variation of light application time.As a comparison, Fig. 2 is that (300nm＜λ＜410nm), acetaldehyde and product carbon dioxide are with the variation of light application time under ultraviolet light for Degussa P25.
The photocatalytic activity of visible light catalyst
A. (λ＞420nm) under the visible light condition
Under the visible light condition, prepared visible light catalyst can be converted into carbon dioxide to acetaldehyde, and exemplary is seen Fig. 6, and 7.Different with other low activity visible light catalyst of having reported, the speed that the acetaldehyde of our prepared visible light catalysts under the visible light condition is converted into carbon dioxide is 0.42 hour
-1, can with the best speed of ultraviolet light catalyst (Degussa P25) under ultraviolet light conditions of the effect that Germany produces (0.56 hour
-1) quite.But as previously mentioned, P25 does not have activity at all under the visible light condition.
B. (300nm＜λ＜410nm) under ultraviolet light conditions
The visible light catalyst of the present invention's preparation not only has considerable activity under the visible light condition, and its activity is (1.3 hours under ultraviolet light conditions
-1) also than the activity (0.56 hour of the ultraviolet light catalyst (Degussa P25) of the marketization
-1) much higher.
The specific embodiment:
Embodiment one
2.4g softex kw and 0.5g dissolution of sodium hydroxide in the 33g deionized water, add the 5g tetraethoxysilance under strong agitation.The 0.12g cobalt nitrate is dissolved in the 5g deionized water, and add in the aforementioned solution.In 100 ℃ of crystallization 5 days, filter in reactor, washing is dried; Dry thing calcined in 550 ℃ of air atmospheres promptly obtained not that supported titanium dioxide is the responsive to visible light type photochemical catalyst of matrix with MCM-41 in 6 hours;
Embodiment two
2.0g softex kw and 0.3g dissolution of sodium hydroxide are in the 30g deionized water; The 0.5g alchlor is water-soluble and add in the aforementioned solution; Under strong agitation, add the 4.5g tetraethoxysilance.The 0.15g cobalt nitrate is dissolved in the 4g deionized water, and add in the aforementioned solution.In 100 ℃ of crystallization 5 days, filter in reactor, washing is dried; Dry thing calcined in 550 ℃ of air atmospheres promptly obtained not that supported titanium dioxide is the responsive to visible light type photochemical catalyst of matrix with AlMCM-41 in 6 hours;
Embodiment three
1.5g example 1 or example 2 gained sample dispersion in the 120ml isopropyl alcohol, are added the 2g titanium isopropoxide thereupon, be stirred to dried; Calcining in 450 ℃ of air atmospheres and promptly obtaining supported titanium dioxide in 3 hours is the responsive to visible light type photochemical catalyst of matrix with MCM-41 or AlMCM-41.
Embodiment four
5.5g softex kw and 1.0g dissolution of sodium hydroxide in the 70g deionized water, add the 15g tetraethoxysilance under strong agitation.The 0.35g chromic nitrate is dissolved in the 8g deionized water, and add in the aforementioned solution.In 100 ℃ of crystallization 5 days, filter in reactor, washing is dried; Dry thing calcined in 550 ℃ of air atmospheres promptly obtained not that supported titanium dioxide is the responsive to visible light type photochemical catalyst of matrix with MCM-41 in 6 hours.
Embodiment five
2.4g softex kw and 0.33g dissolution of sodium hydroxide are in the 30g deionized water; The 0.25g alchlor is water-soluble and add in the aforementioned solution; Under strong agitation, add the 6.5g tetraethoxysilance.The 0.2g manganese nitrate is dissolved in the 5g deionized water, and add in the aforementioned solution.In 100 ℃ of crystallization 5 days, filter in reactor, washing is dried; Dry thing calcined in 550 ℃ of air atmospheres promptly obtained not that supported titanium dioxide is the responsive to visible light type photochemical catalyst of matrix with AlMCM-41 in 6 hours;
Embodiment six
7.0g softex kw and 1.0g dissolution of sodium hydroxide in the 60g deionized water, add the 12g tetraethoxysilance under strong agitation.The 0.25g ferric nitrate is dissolved in the 6g deionized water, and add in the aforementioned solution.In 100 ℃ of crystallization 5 days, filter in reactor, washing is dried; Dry thing calcined in 550 ℃ of air atmospheres promptly obtained not that supported titanium dioxide is the responsive to visible light type photochemical catalyst of matrix with MCM-41 in 6 hours.
The present invention compares with all patents of seeing and document, does not need expensive device, with visible light catalyst＞420nm can See that the effect under the light is quite active with the ultraviolet light catalyst (Degussa P25) of the marketization, and at 300nm＜λ＜410nm Activity under the ultraviolet light is better than Degussa P25 greatly. Can be used for the removal of air and indoor aldehydes.
Claims (6)
1, with the sial mesopore molecular sieve is the visible light catalyst of matrix, be to be matrix with sial mesopore molecular sieve MCM-41 and AlMCM-41, it is characterized in that: according to silicon: aluminium: transition metal=55-95%: 1-10%: 0.1-1% is doped with transition metal, supported titanium dioxide or not supported titanium dioxide all can.
2, according to the described visible light catalyst of claim 1, it is characterized in that: specific area is at 500-1000m
2Between/the g, pore volume is at 0.4-0.8cm
3Between/the g, average pore diameter is between 2.2-3.3nm.
3,, it is characterized in that described transition metal includes manganese, iron, chromium, cobalt, nickel, vanadium, tungsten according to the described visible light catalyst of claim 1.
4,, it is characterized in that and the MCM-41 aperture similar other mesoporous material that as MCM-48, HMS, the TiMCM-41 material also can be used as matrix at 2-10nm with the AlMCM-41 matrix according to the described visible light catalyst of claim 1.
5, a kind of preparation method of visible light catalyst according to claim 1 is characterized in that:
A. softex kw and dissolution of sodium hydroxide in deionized water;
B. in a, add tetraethoxysilance;
The soluble-salt of transition metal that c. will be to be mixed dissolves in the appropriate amount of deionized water by solubility, waits to dissolve the back and adds among a;
D. with above-mentioned mixed liquor in reactor in 90-120 ℃ of crystallization 5-7 days, filter, washing is dried;
E. dry thing is calcined in 500-600 ℃ of air atmosphere and promptly obtained not that supported titanium dioxide is the visible light catalyst of matrix with MCM-41 in 6 hours;
F. alchlor is water-soluble and add among a, repeat b-e, promptly obtaining not, supported titanium dioxide is the visible light catalyst of matrix with AlMCM-41;
G. with e or f gained sample dispersion in the pure isopropyl alcohol of reagent, add titanium isopropoxide, be stirred to dried;
H. dry thing being calcined in 400-500 ℃ of air atmosphere and promptly being obtained supported titanium dioxide in 3 hours is the visible light catalyst of matrix with MCM-41 or AlMCM-41.
6,, it is characterized in that soluble-salt comprises villaumite, nitrate, acetate according to the preparation method of the described visible light catalyst of claim 4.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB031172520A CN1189243C (en) | 2003-01-25 | 2003-01-25 | Visible light catalyst with molecular sieve of silica-alumina media poves as substrate and its preparing method |
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| CNB031172520A CN1189243C (en) | 2003-01-25 | 2003-01-25 | Visible light catalyst with molecular sieve of silica-alumina media poves as substrate and its preparing method |
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| CN1189243C CN1189243C (en) | 2005-02-16 |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1297478C (en) * | 2003-11-28 | 2007-01-31 | 上海家化联合股份有限公司 | Molecular sieve based nano composite anti-ultraviolet material, its preparation method and use |
| CN101760272A (en) * | 2010-01-08 | 2010-06-30 | 浙江大学 | Method for removing hydrogen sulfide in methane by photocatalytic oxidation |
| CN101733139B (en) * | 2009-12-28 | 2011-06-22 | 哈尔滨工业大学 | Method for preparing nano TiO2/SBA-15 photocatalyst |
| CN110252384A (en) * | 2019-06-20 | 2019-09-20 | 大连理工大学 | A kind of sub-nanometer cluster transition metal oxide/MCM-41 composite material, preparation method and applications |
-
2003
- 2003-01-25 CN CNB031172520A patent/CN1189243C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1297478C (en) * | 2003-11-28 | 2007-01-31 | 上海家化联合股份有限公司 | Molecular sieve based nano composite anti-ultraviolet material, its preparation method and use |
| CN101733139B (en) * | 2009-12-28 | 2011-06-22 | 哈尔滨工业大学 | Method for preparing nano TiO2/SBA-15 photocatalyst |
| CN101760272A (en) * | 2010-01-08 | 2010-06-30 | 浙江大学 | Method for removing hydrogen sulfide in methane by photocatalytic oxidation |
| CN110252384A (en) * | 2019-06-20 | 2019-09-20 | 大连理工大学 | A kind of sub-nanometer cluster transition metal oxide/MCM-41 composite material, preparation method and applications |
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|---|---|
| CN1189243C (en) | 2005-02-16 |
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