CN104190407B - Visible light-responded photocatalyst SrBi2w6o22and preparation method thereof - Google Patents
Visible light-responded photocatalyst SrBi2w6o22and preparation method thereof Download PDFInfo
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- CN104190407B CN104190407B CN201410493068.8A CN201410493068A CN104190407B CN 104190407 B CN104190407 B CN 104190407B CN 201410493068 A CN201410493068 A CN 201410493068A CN 104190407 B CN104190407 B CN 104190407B
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Abstract
The invention discloses a kind of visible light-responded photocatalyst SrBi2W6O22And preparation method thereof.The chemical constitution formula of this photocatalyst is SrBi2W6O22.The invention also discloses the preparation method of above-mentioned material.The photocatalyst that the present invention obtains has the advantages such as spectral response range width, light conversion efficiency height and good stability and has decomposition harmful chemical, organic-biological matter and the effect of sterilization under visible light illumination；Additionally preparation method is simple, synthesis temperature is low, low cost, is suitable for commercial production and application.
Description
Technical field
The present invention relates to a kind of visible light-responded photocatalyst SrBi2W6O22And preparation method thereof, belong to inorganic field of photocatalytic material.
Background technology
Along with socioeconomic development, people increasingly pay close attention to for the energy and ecological environment, solve energy shortage and problem of environmental pollution be realize sustainable development, improve people's living standard and safeguard national security in the urgent need to.
From phase late 1970s, there has been proposed and utilize in photocatalyst decomposition water and the Organic substance such as pesticide in air and odorant, and scribble the application example such as self-cleaning of the surface of solids of photocatalyst.The principle of light-catalyzed reaction be photocatalyst after absorbing higher than the photon of its band-gap energy, generate hole and electronics, these holes and electronics carry out oxidation reaction and reduction reaction respectively, reach to decompose harmful chemical, organic-biological matter and the purpose of sterilization.Photocatalyst has many kinds, and the most most representative is titanium dioxide (TiO2), utilize titanium dioxide that the Organic substances such as the pesticide in water and in air and odorant are decomposed, but the band gap of titanium dioxide is 3.2eV, under the ultraviolet irradiation shorter than 400nm, only just can show activity, can only be at indoor or the local work having uviol lamp, being little to utilize visible ray, this greatly limits the use of titanium dioxide optical catalyst.
In view of photocatalyst practicality in decomposing harmful substances, it is indispensable for utilizing sunlight as light source.Irradiate the sunlight medium wavelength maximum intensity of visible ray near 500nm to earth's surface, wavelength is that the energy of the visible region of 400nm ~ 750nm is about the 43% of sunlight gross energy, so in order to utilize efficiently, the R and D of bismuth series photocatalyst have been achieved for a series of great achievement, bismuthous complex such as BiVO4、Bi2MoO6、Bi2Mo2O9、Bi2Mo3O12And Bi2WO4It is in the news and there is good absorption under visible light.A series of niobiums (tantalum) hydrochlorate photocatalyst is widely studied owing to having higher photocatalytic activity.Such as, niobate photocatalyst Pb3Nb4O13、BiNbO4And Bi2MNbO7(M=Al, Ga, In, Y, rare earth element and Fe) etc. and niobium potassium compound oxide photocatalyst such as KNbO3、KNb3O8、K4Nb6O17And K6Nb10.6O30Deng all having preferable photocatalysis performance.
Although photocatalysis research has been carried out the several years, but at present report to have visible light-responded photocatalyst kind the most limited, there are still that light conversion efficiency is low, poor stability and the problem such as spectral response range is narrow, so it is the most necessary for researching and developing the new visible light-responded high efficiency photocatalyst that has.We are to consisting of BaBi2W6O22、SrBi2W6O22、CaBi2W6O22、PbBi2W6O22Compound carried out Photocatalytic Performance Study, found that SrBi2W6O22Band gap be 2.73 eV, have excellence visible light-responded photocatalysis performance, the band gap width of other sample is both greater than 3.0eV, just can only can show activity under ultraviolet irradiation.
Summary of the invention
It is an object of the invention to provide and a kind of there is visible light-responded photocatalyst SrBi2W6O22And preparation method thereof.
The chemical constitution formula with visible light-responded photocatalyst that the present invention relates to is: SrBi2W6O22。
The preparation method of above-mentioned visible light-responded photocatalyst concretely comprises the following steps:
(1) by 99.9% analytically pure chemical raw material SrCO3、Bi2O3And WO3Starting powder press SrBi2W6O22Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and distilled water, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) by the powder of step (2) mix homogeneously 850 ~ 900 DEG C of pre-burnings, and it is incubated 6 hours, naturally cools to room temperature, then pulverize means by ball mill and make average diameter of particles diminish, less than 2 μm, i.e. obtain SrBi2W6O22Powder.
The spectral response range width of the photocatalyst that the present invention obtains, light conversion efficiency height and good stability, there is decomposition harmful chemical, organic-biological matter and the effect of sterilization under visible light illumination；Additionally preparation method is simple, synthesis temperature is low, low cost, is suitable for commercial production and application.
Detailed description of the invention
Present invention will be described in detail below:
1, in order to obtain the composite oxides used in the present invention, prepare powder first by solid-phase synthesis, i.e. various oxides or the carbonate as raw material is mixed according to target constitutional chemistry metering ratio, then synthesize in air atmosphere at ambient pressure.
2 in order to effectively utilize light, the size of the photocatalyst in the present invention preferably in micron level, even nanoparticle, and specific surface area is bigger.The oxide powder prepared with solid-phase synthesis, its particle is relatively big and surface area is less, but can be by ball mill pulverizing means and make particle diameter diminish.
3, the photocatalysis experiment of the present invention is using methyl orange as simulation organic pollution, and its concentration is 20mg/L；Photocatalyst SrBi2W6O22Addition be 1g/L；Light source uses the xenon lamp of 300W, and reactive tank uses the vessel that pyrex is made, and obtains the wavelength light more than 420nm long wavelength by wave filter, then irradiates photocatalyst；Catalysis time is set as 60 minutes.
Embodiment 1:
(1) by 99.9% analytically pure chemical raw material SrCO3、Bi2O3And WO3Starting powder press SrBi2W6O22Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and distilled water, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) by the powder of step (2) mix homogeneously 850 DEG C of pre-burnings, and it is incubated 6 hours, naturally cools to room temperature, then pulverize means by ball mill and make average diameter of particles diminish, less than 2 μm, i.e. obtain SrBi2W6O22Powder.
Prepared photocatalyst, under the wavelength radiation of visible light more than 420nm, reaches 97.6% to methyl orange clearance in 60 minutes.
Embodiment 2:
(1) by 99.9% analytically pure chemical raw material SrCO3、Bi2O3And WO3Starting powder press SrBi2W6O22Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and distilled water, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) by the powder of step (2) mix homogeneously 880 DEG C of pre-burnings, and it is incubated 6 hours, naturally cools to room temperature, then pulverize means by ball mill and make average diameter of particles diminish, less than 2 μm, i.e. obtain SrBi2W6O22Powder.
Prepared photocatalyst, under the wavelength radiation of visible light more than 420nm, reaches 97.3% to methyl orange clearance in 60 minutes.
Embodiment 3:
(1) by 99.9% analytically pure chemical raw material SrCO3、Bi2O3And WO3Starting powder press SrBi2W6O22Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and distilled water, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) by the powder of step (2) mix homogeneously 900 DEG C of pre-burnings, and it is incubated 6 hours, naturally cools to room temperature, then pulverize means by ball mill and make average diameter of particles diminish, less than 2 μm, i.e. obtain SrBi2W6O22Powder.
Prepared photocatalyst, under the wavelength radiation of visible light more than 420nm, 60min reaches 98.1% to methyl orange clearance.
The present invention is never limited to above example.The bound of each temperature, interval value can realize the present invention, embodiment numerous to list herein.
The made photocatalyst powder of above inventive embodiments can be carried on multiple matrix surface.Matrix can be glass, pottery, activated carbon or quartz sand etc., and photocatalyst can be carried on matrix surface in the form of a film.
Claims (1)
1. a visible light-responded photocatalyst, it is characterised in that the chemical constitution formula of described photocatalyst is SrBi2W6O22；
The preparation method of described photocatalyst concretely comprises the following steps:
(1) by 99.9% analytically pure chemical raw material SrCO3、Bi2O3And WO3Starting powder press SrBi2W6O22Composition weigh dispensing；
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and distilled water, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves；
(3) by the powder of step (2) mix homogeneously 850 ~ 900 DEG C of pre-burnings, and it is incubated 6 hours, naturally cools to room temperature, then pulverize means by ball mill and make average diameter of particles be less than 2 μm, i.e. obtain SrBi2W6O22Powder.
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| CN104624182A (en) * | 2015-01-13 | 2015-05-20 | 三峡大学 | Visible-light response photo catalyst Sr3Li3BiW2O12 and preparation method thereof |
| CN104874391A (en) * | 2015-05-23 | 2015-09-02 | 桂林理工大学 | Visible light responding photocatalyst SrLiBi3W5O21 and preparation method thereof |
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| JP2012140275A (en) * | 2010-12-28 | 2012-07-26 | Ohara Inc | Glass ceramic and production method therefor |
| CN103433030B (en) * | 2013-09-05 | 2016-01-13 | 桂林理工大学 | Visible light-responded tungstates photochemical catalyst Sr 2wO 5and preparation method thereof |
| CN103495411A (en) * | 2013-09-23 | 2014-01-08 | 桂林理工大学 | Visible-light response photocatalyst Sr2Bi3V3O14 and preparation method thereof |
| CN103551140B (en) * | 2013-11-11 | 2016-03-02 | 桂林理工大学 | Visible light-responded photochemical catalyst Sr 6w 2v 2o 17and preparation method thereof |
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Effective date of registration: 20201208 Address after: No.25-1, Gangcheng Road, dongyinggang Economic Development Zone, Hekou District, Dongying City, Shandong Province Patentee after: Shandong Xingqiang Chemical Industry Technology Research Institute Co.,Ltd. Address before: Room 502, building 1, No. 40, xiayuangang East Street, Tianhe District, Guangzhou City, Guangdong Province Patentee before: Guangzhou Boyi Intellectual Property Operation Co.,Ltd. Effective date of registration: 20201208 Address after: Room 502, building 1, No. 40, xiayuangang East Street, Tianhe District, Guangzhou City, Guangdong Province Patentee after: Guangzhou Boyi Intellectual Property Operation Co.,Ltd. Address before: 541004 the Guangxi Zhuang Autonomous Region Guilin Construction Road No. 12 Patentee before: GUILIN University OF TECHNOLOGY |