CN102205247B - Composite oxide photocatalyst LiCuNb3-xTaxO9 with visible light response and preparation method thereof - Google Patents
Composite oxide photocatalyst LiCuNb3-xTaxO9 with visible light response and preparation method thereof Download PDFInfo
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- CN102205247B CN102205247B CN201110075001A CN201110075001A CN102205247B CN 102205247 B CN102205247 B CN 102205247B CN 201110075001 A CN201110075001 A CN 201110075001A CN 201110075001 A CN201110075001 A CN 201110075001A CN 102205247 B CN102205247 B CN 102205247B
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- visible light
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Abstract
The invention discloses a composite oxide photocatalyst with visible light response. The general formula of the chemical composition of the composite oxide photocatalyst is LiCuNb3-xTaxO9, and x is more than or equal to 0 and less than or equal to 3. The composite oxide photocatalyst is prepared by the following steps of: weighing and proportioning 99.9 percent analytically pure chemical raw materials such as Li2CO3, CuO, Nb2O5 and Ta2O5 according to the chemical formula LiCuNb3-xTaxO9, wherein x is more than or equal to 0 and less than or equal to 3; mixing the proportioned raw materials, putting the raw materials into a ball milling jar, adding zirconia spheres and anhydrous ethanol, performing ball milling for 12 hours, mixing, grinding, taking out, drying, and sieving with a sieve of 200 meshes; pre-sintering the uniformly mixed powder at the temperature of between 800 and 1,000 DEG C, preserving the heat for 8 to 10 hours, naturally cooling to room temperature, reducing the diameters of the particles by crushing through a ball mill and the like till the diameters of the particles are less than 2 microns to obtain composite oxide photocatalyst LiCuNb3-xTaxO9 powder. The preparation method is simple and low in cost; and the prepared photocatalyst has excellent catalytic performance, has the effect of decomposing harmful chemical substances under the irradiation of visible light, and has good stability and good application prospect.
Description
Technical field
The present invention relates to a kind of visible light responded composite oxide photocatalyst LiCuNb
3-xTa
xO
9(0≤x≤3) and preparation method thereof belong to inorganic field of photocatalytic material.
Background technology
Along with The development in society and economy, people more and more pay close attention to for the energy and ecological environment, solve energy shortage and problem of environmental pollution and be to realize sustainable development, raising people's living standard and pressing for of safeguarding national security.
From phase late 1970s, people proposed to utilize in the photochemical catalyst decomposition water with atmosphere in organic matters such as agricultural chemicals and odorant, and application examples such as self-cleaning that scribble the surface of solids of photochemical catalyst.The principle of light-catalyzed reaction is that photochemical catalyst is after having absorbed the photon that is higher than its band-gap energy; Hole and electronics have been generated; These holes and electronics carry out oxidation reaction and reduction reaction respectively, reach the purpose of decomposing harmful chemical, organic-biological matter and sterilization.Photochemical catalyst has many kinds, and wherein most representative is titanium dioxide (TiO
2); Utilized titanium dioxide in the water with atmosphere in organic matters such as agricultural chemicals and odorant decompose; Yet the band gap of titanium dioxide is 3.2eV, only under the ultraviolet irradiation shorter than 400nm, just can show activity, can only be indoor or the local work of uviol lamp arranged; Almost can not utilize visible light, this has limited the use of titanium dioxide optical catalyst greatly.
Consider the practicality of photochemical catalyst in decomposing harmful substances, utilizing sunshine is indispensable as light source.Irradiation is maximum near sunshine medium wavelength visible light intensity 500nm on the face of land; Wavelength is that the energy of the visible region of 400nm-750nm approximately is 43% of a sunshine gross energy; So in order to utilize solar spectrum efficiently, searching has the attention that visible light-responded photochemical catalyst has caused people.
Catalysis material is having important application prospects aspect the solution energy and the environmental problem.In the last few years; Photochemical catalyst has caused countries in the world scientist's concern; Many famous research institutions and enterprise drop into the research that huge fund is engaged in photochemical catalyst mechanism and application in succession, and photochemical catalyst has begun to get in many fields such as antibiotic, deodorization, antifouling and water treatments to be applied the stage.Some scientists think that because photochemical catalyst has good depollution of environment effect, along with going deep into of various countries' research work, this new material will become one of 21 century brand-new material product the most likely.
Though photocatalysis research has been carried out the several years; But at present report to have visible light-responded photochemical catalyst kind still very limited; Problem such as exist still that light conversion efficiency is low, poor stability and spectrum respective range are narrow is very necessary so research and develop the new visible light-responded high efficiency photocatalyst that has.
Summary of the invention
The purpose of this invention is to provide a kind of have visible light responded composite oxide photocatalyst and preparation method.
Provided by the invention have a visible light responded composite oxide photocatalyst, and its chemical composition general formula is: LiCuNb
3-xTa
xO
9, 0≤x≤3 wherein.
The preparation method of above-mentioned visible light responded composite oxide photocatalyst, carry out according to the following steps:
1) with 99.9% analytically pure chemical raw material Li
2CO
3, CuO, Nb
2O
5And Ta
2O
5, press LiCuNb
3-xTa
xO
9Chemical formula weigh batching, wherein 0≤x≤3;
2) step (1) confected materials is mixed, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 12h mixes levigately, takes out oven dry, 200 mesh sieves;
3) powder that step (2) is mixed is 800-1000 ℃ of pre-burning, and is incubated 8 one 10h, naturally cools to room temperature, through pulverizing means such as ball mills particle diameter diminished then, is lower than 2 μ m, can obtain composite oxide photocatalyst Li CuNb
3-xTa
xO
9Powder.
Preparation method of the present invention is simple, cost is low, and the photochemical catalyst of preparation has excellent catalytic performance, under radiation of visible light, has the effect of decomposing harmful chemical, organic-biological matter and sterilization.
The specific embodiment
To specify the present invention below:
1, in order to obtain employed composite oxides among the present invention, at first use solid-phase synthesis to prepare powder, promptly mix various oxides or carbonate according to target composition stoichiometric proportion as raw material, synthetic in air atmosphere under normal pressure again.
2, in order effectively to utilize light, the size of the photochemical catalyst among the present invention is preferably in micron level, or even nano particle, and specific area is bigger.With the oxide powder of solid-phase synthesis preparation, its particle is big and surface area is less, but can particle diameter diminished through pulverizing means such as ball mills.
3, as the simulation organic pollution, its concentration is 20mg/L with methyl orange in photocatalysis experiment of the present invention; The addition of bismuth-system compound oxide photocatalyst is 1g/L; Light source uses the xenon lamp of 300W, and the vessel that reactive tank uses pyrex to process obtain the light of wavelength greater than 420nm long wavelength, irradiates light catalyst then through wave filter; The catalysis time set is 120min.
Embodiment 1:
1) with 99.9% analytically pure chemical raw material Li
2CO
3, CuO, Nb
2O
5, press LiCuNb
3O
9The chemical formula weigh batching;
2) confected materials is mixed, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 12h mixes levigately, takes out oven dry, 200 mesh sieves;
3) the above-mentioned powder that mixes is 800 ℃ of pre-burnings, and insulation 8h, naturally cools to room temperature, through pulverizing means such as ball mills particle diameter diminished then, is lower than 2 μ m, can obtain composite oxide photocatalyst Li CuNb
3O
9Powder.
Prepared photochemical catalyst, under the radiation of visible light of wavelength greater than 420nm, 120min reaches 97.8% to the methyl orange clearance.
Embodiment 2:
1) with 99.9% analytically pure chemical raw material Li
2CO
3, CuO, Ta
2O
5, press LiCuTa
3O
9The chemical formula weigh batching;
2) confected materials is mixed, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 12h mixes levigately, takes out oven dry, 200 mesh sieves;
3) the above-mentioned powder that mixes is 1000 ℃ of pre-burnings, and insulation 10h, naturally cools to room temperature, through pulverizing means such as ball mills particle diameter diminished then, is lower than 2 μ m, can obtain composite oxide photocatalyst Li CuTa
3O
9Powder.
Prepared photochemical catalyst, under the radiation of visible light of wavelength greater than 420nm, 120min reaches 98.8% to the methyl orange clearance.
Embodiment 3:
1) with 99.9% analytically pure chemical raw material Li
2CO
3, CuO, Nb
2O
5, Ta
2O
5, press LiCuNb
2TaO
9The chemical formula weigh batching;
2) confected materials is mixed, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 12h mixes levigately, takes out oven dry, 200 mesh sieves;
3) the above-mentioned powder that mixes is 850 ℃ of pre-burnings, and insulation 9h, naturally cools to room temperature, through pulverizing means such as ball mills particle diameter diminished then, is lower than 2 μ m, can obtain composite oxide photocatalyst Li CuNb
2TaO
9Powder.
Prepared photochemical catalyst, under the radiation of visible light of wavelength greater than 420nm, 120min reaches 97.6% to the methyl orange clearance.
Embodiment 4:
1) with 99.9% analytically pure chemical raw material Li
2CO
3, TiO
2, Nb
2O
5, Ta
2O
5, press LiCuNbTa
2O
9The chemical formula weigh batching.
2) chemical raw material for preparing is mixed, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 12h mixes levigately, takes out oven dry, 200 mesh sieves.
3) the above-mentioned powder that mixes is 920 ℃ of pre-burnings, and insulation 9h, naturally cools to room temperature, pulverizes through ball mill then particle diameter is diminished, and reaches about 2 μ m, can obtain composite oxide photocatalyst Li CuNbTa
2O
9Powder.
Prepared photochemical catalyst, under the radiation of visible light of wavelength greater than 420nm, 120min reaches 98.2% to the methyl orange clearance.
The present invention never is limited to above embodiment.Have and Nb, the element of Ta analog structure and chemical property such as V, Sb etc. also can make the photochemical catalyst with analogous crystalline structure of the present invention and performance.The bound of each raw material, interval value, and the bound of technological parameter (like temperature, time etc.), interval value can both realize the present invention, do not enumerate embodiment one by one at this.
The made photocatalyst powder of above inventive embodiments can be carried on the multiple matrix surface.Matrix can be glass, pottery, active carbon, quartz sand etc., and photochemical catalyst can be carried on matrix surface with the form of film.
Claims (1)
1. composite oxides is characterized in that the chemical composition general formula of said composite oxides is: LiCuNb in visible light-responded Application in Photocatalysis
3-xTa
xO
9, 0≤x≤3 wherein;
The preparation method of described composite oxides is characterized in that step is:
1) with 99.9% analytically pure chemical raw material Li
2CO
3, CuO, Nb
2O
5And Ta
2O
5, press LiCuNb
3-xTa
xO
9Chemical formula weigh batching, wherein 0≤x≤3;
2) step (1) confected materials is mixed, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 12h mixes levigately, takes out oven dry, 200 mesh sieves;
3) powder that step (2) is mixed is 800-1000 ℃ of pre-burning, and insulation 8-10h, naturally cools to room temperature, through ball mill pulverizing means particle diameter is diminished then, is lower than 2 μ m, can obtain composite oxide photocatalyst Li CuNb
3-xTa
xO
9Powder.
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CN103157458B (en) * | 2013-04-01 | 2015-04-15 | 桂林理工大学 | Visible-light-responsive tantalate photocatalyst LiMTa3O9 and preparation method thereof |
CN103495423A (en) * | 2013-09-23 | 2014-01-08 | 桂林理工大学 | Visible-light response wolframate photocatalyst Li2CuW2O8 and preparation method thereof |
CN103877968B (en) * | 2014-04-07 | 2016-05-18 | 桂林理工大学 | Visible light-responded photocatalyst Li3Nb3Si2O13And preparation method thereof |
CN104069866A (en) * | 2014-06-30 | 2014-10-01 | 桂林理工大学 | Photocatalyst LiCu2V3O10 in response to visible light and preparation method thereof |
CN104383936A (en) * | 2014-11-12 | 2015-03-04 | 桂林理工大学 | Photocatalyst Li2Cu2Ge2O7 with visible light response and preparation method thereof |
CN104667942A (en) * | 2015-02-26 | 2015-06-03 | 桂林理工大学 | Photocatalyst LiCuNb5O14 with visible light response and preparation method thereof |
CN104646004A (en) * | 2015-02-26 | 2015-05-27 | 桂林理工大学 | Photocatalyst LiCu2Nb7O20 with visible light response and preparation method thereof |
CN104722309B (en) * | 2015-03-06 | 2016-11-02 | 三峡大学 | Visible light-responded photochemical catalyst K2ni2sb8o23and preparation method thereof |
CN104741129A (en) * | 2015-03-06 | 2015-07-01 | 三峡大学 | Visible light responding photocatalyst LiCuTa5O14 and preparation method thereof |
CN104722310A (en) * | 2015-03-06 | 2015-06-24 | 三峡大学 | Visible-light-responded photocatalyst LiCu2Ta7O20 and preparation method thereof |
CN105561972A (en) * | 2015-12-22 | 2016-05-11 | 桂林理工大学 | Visible-light-response photocatalyst LiTaGeO5 and preparation method thereof |
CN105688887A (en) * | 2016-01-13 | 2016-06-22 | 三峡大学 | Visible-light response photocatalyst BaLi4Ge5O13 and preparation method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1618516A (en) * | 2004-09-28 | 2005-05-25 | 北京联合大学生物化学工程学院 | Composite nano-photo-catalyst used for purifying air |
CN101402043A (en) * | 2008-10-30 | 2009-04-08 | 大连理工大学 | Visible light photocatalysis air purification material and air purification method |
-
2011
- 2011-03-24 CN CN201110075001A patent/CN102205247B/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1618516A (en) * | 2004-09-28 | 2005-05-25 | 北京联合大学生物化学工程学院 | Composite nano-photo-catalyst used for purifying air |
CN101402043A (en) * | 2008-10-30 | 2009-04-08 | 大连理工大学 | Visible light photocatalysis air purification material and air purification method |
Non-Patent Citations (1)
Title |
---|
Mineo Sato等.Structure of New Perovskite-related Compounds, LiCuM3O9(M=Nb,Ta).《J. MATER. CHEM.》.1993,第3卷(第3期),233-236. * |
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