CN104722309A - Visible-light-responded photocatalyst K2Ni2Sb8O23 and preparation method thereof - Google Patents
Visible-light-responded photocatalyst K2Ni2Sb8O23 and preparation method thereof Download PDFInfo
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- CN104722309A CN104722309A CN201510099374.8A CN201510099374A CN104722309A CN 104722309 A CN104722309 A CN 104722309A CN 201510099374 A CN201510099374 A CN 201510099374A CN 104722309 A CN104722309 A CN 104722309A
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Abstract
The invention discloses a broadband and efficient visible-light-responded photocatalyst K2Ni2Sb8O23 and a preparation method thereof. The chemical composition formula of the photocatalyst is K2Ni2Sb8O23. The invention further discloses the preparation method of the photocatalyst. The photocatalyst disclosed by the invention has the advantages of wide spectral response range, high light conversion efficiency, good stability and the like; the photocatalyst plays a role in decomposing harmful chemical substances and organic biomass and sterilizing under the irradiation of visible light; in addition, the preparation method is simple, is low in synthesis temperature and low in cost and is applicable to industrial production and application.
Description
Technical field
The present invention relates to a kind of visible light-responded photochemical catalyst K
2ni
2sb
8o
23and preparation method thereof, belong to inorganic field of photocatalytic material.
Background technology
Along with socioeconomic development, people more and more 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 to utilize in photochemical catalyst decomposition water and the organic matter such as agricultural chemicals in air and odorant, and scribble the application example such as self-cleaning of the surface of solids of photochemical catalyst.The principle of light-catalyzed reaction is that photochemical catalyst is after absorbing the photon higher than its band-gap energy, generate hole and electronics, these holes and electronics carry out oxidation reaction and reduction reaction respectively, reach the object of decomposing harmful chemical, organic-biological matter and sterilization.Photochemical catalyst has many kinds, and wherein most representative is titanium dioxide (TiO
2), titanium dioxide has been utilized to decompose organic matters such as the agricultural chemicals in water and in air and odorants, but the band gap of titanium dioxide is 3.2eV, only under the ultraviolet irradiation shorter than 400nm, just activity can be shown, can only at indoor or the local work having uviol lamp, almost can not utilize visible ray, this limits the use of titanium dioxide optical catalyst greatly.
Consider the practicality of photochemical catalyst in decomposing harmful substances, utilize sunshine to be indispensable as light source.Irradiate maximum to sunshine medium wavelength intensity of visible ray near 500nm on earth's surface, wavelength is the energy of the visible region of 400nm ~ 750nm is approximately 43% of sunshine gross energy, so in order to efficient utilization, the R and D of bismuth series photocatalyst have achieved a series of great achievement, and bismuthous compound is as BiVO
4, Bi
2moO
6, Bi
2mo
2o
9, Bi
2mo
3o
12and Bi
2wO
4be in the news and there is good absorption under visible light.A series of niobium (tantalum) hydrochlorate photochemical catalyst is widely studied owing to having higher photocatalytic activity.Such as, niobate photocatalyst Pb
3nb
4o
13, BiNbO
4and Bi
2mNbO
7(M=Al, Ga, In, Y, rare earth element and Fe) etc. with niobium potassium compound oxide photocatalyst as KNbO
3, KNb
3o
8, K
4nb
6o
17and K
6nb
10.6o
30deng all, there is good photocatalysis performance, but its intrinsic photocatalytic effect is very weak or do not have activity in visible-range.
Although photocatalysis research has carried out the several years, the current exploration to visible light-responded photochemical catalyst is the summary of experience drawn by great many of experiments with exploitation major part, in theory also cannot from the crystal structure of compound, composition, the physicochemical properties such as molecular weight are predicted its photocatalysis performance, therefore at present report to have visible light-responded photochemical catalyst kind still very limited, and it is low to there is light conversion efficiency, synthesis difficulty, poor stability and the problem such as spectral response range is narrow, research and develop that new preparation method is simple and to have the visible light-responded high efficiency photocatalyst of wideband be that this area scientific and technical personnel thirst for solving always but are difficult to the difficult problem that succeeds all the time, which greatly limits extensive use and the development of photochemical catalyst.We are to consisting of K
2ni
2sb
8o
23, Li
2ni
2sb
8o
23and K
2zn
2sb
8o
23sample carried out Photocatalytic Performance Study.Found that K
2ni
2sb
8o
23band gap width is 2.49eV, has excellent visible light-responded photocatalysis performance; Li
2ni
2sb
8o
23and K
2zn
2sb
8o
23for insulator, under ultraviolet irradiation, also do not show activity.
Summary of the invention
The object of this invention is to provide and a kind of there is visible light-responded photochemical catalyst K
2ni
2sb
8o
23and preparation method thereof.
The chemical constitution formula with visible light-responded photochemical catalyst that the present invention relates to is: K
2ni
2sb
8o
23.
Preparation method's concrete steps of above-mentioned visible light-responded photochemical catalyst are:
(1) by 99.9% analytically pure chemical raw material K
2cO
3, NiO and Sb
2o
5starting powder press K
2ni
2sb
8o
23composition weigh batching.
(2) raw material mixing step (1) prepared, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) mixed 950 ~ 1000 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, is then pulverized by ball mill and average diameter of particles is diminished, lower than 2 μm, namely obtain K
2ni
2sb
8o
23powder.
Advantage of the present invention: K
2ni
2sb
8o
23the visible light-responded wide frequency range of photochemical catalyst, the high and good stability of light conversion efficiency, has the effect of decomposing harmful chemical, organic-biological matter and sterilization under visible light illumination; Preparation method is simple in addition, synthesis temperature is low, and cost is low, is applicable to industrial production and application.
Detailed description of the invention
To be specifically described the present invention below:
1, in order to obtain the composite oxides used in the present invention, first use solid-phase synthesis to prepare powder, namely using as the various oxide of raw material or carbonate according to the metering of target constitutional chemistry than mixing, then to synthesize in air atmosphere at ambient pressure.
2, in order to effectively utilize light, the size of the photochemical catalyst in the present invention is preferably in micron level, or even nano particle, and specific area is larger.With oxide powder prepared by solid-phase synthesis, its particle is comparatively large and surface area is less, but can pulverize means by ball mill makes particle diameter diminish.
3, photocatalysis experiment of the present invention is using methyl orange as simulation organic pollution, and its concentration is 20mg/L; Photochemical catalyst K
2ni
2sb
8o
23addition be 1g/L; Light source uses the xenon lamp of 300W, the vessel that reactive tank uses pyrex to make, and obtains the light that wavelength is greater than 420nm, then irradiate photochemical catalyst by wave filter; Catalysis time is set as 60 minutes.
Embodiment 1:
(1) by 99.9% analytically pure chemical raw material K
2cO
3, NiO and Sb
2o
5starting powder press K
2ni
2sb
8o
23composition weigh batching.
(2) raw material mixing step (1) prepared, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) mixed 950 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, is then pulverized by ball mill and average diameter of particles is diminished, lower than 2 μm, namely obtain K
2ni
2sb
8o
23powder.
Prepared photochemical catalyst, under being greater than the radiation of visible light of 420nm, reaches 97.2% to methyl orange clearance in 60 minutes at wavelength.
Embodiment 2:
(1) by 99.9% analytically pure chemical raw material K
2cO
3, NiO and Sb
2o
5starting powder press K
2ni
2sb
8o
23composition weigh batching.
(2) raw material mixing step (1) prepared, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) mixed 980 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, is then pulverized by ball mill and average diameter of particles is diminished, lower than 2 μm, namely obtain K
2ni
2sb
8o
23powder.
Prepared photochemical catalyst, under being greater than the radiation of visible light of 420nm, reaches 98.7% to methyl orange clearance in 60 minutes at wavelength.
Embodiment 3:
(1) by 99.9% analytically pure chemical raw material K
2cO
3, NiO and Sb
2o
5starting powder press K
2ni
2sb
8o
23composition weigh batching.
(2) raw material mixing step (1) prepared, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) mixed 1000 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, is then pulverized by ball mill and average diameter of particles is diminished, lower than 2 μm, namely obtain K
2ni
2sb
8o
23powder.
Prepared photochemical catalyst, be greater than the radiation of visible light of 420nm at wavelength under, 60min reaches 98.2% to methyl orange clearance.
The present invention is never limited to above embodiment.Bound, the interval value of each temperature can realize the present invention, do not enumerate embodiment at this.
The made photocatalyst powder of above inventive embodiments can be carried on multiple matrix surface.Matrix can be glass, pottery, active carbon or quartz sand etc., and photochemical catalyst can be carried on matrix surface in the form of a film.
Claims (1)
1. a visible light-responded photochemical catalyst, is characterized in that the chemical constitution formula of described photochemical catalyst is K
2ni
2sb
8o
23;
Preparation method's concrete steps of described photochemical catalyst are:
(1) by 99.9% analytically pure chemical raw material K
2cO
3, NiO and Sb
2o
5starting powder press K
2ni
2sb
8o
23composition weigh batching;
(2) raw material mixing step (1) prepared, put into ball grinder, add zirconia ball and absolute ethyl alcohol, ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves;
(3) powder step (2) mixed 950 ~ 1000 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, is then pulverized by ball mill and makes average diameter of particles lower than 2 μm, namely obtain K
2ni
2sb
8o
23powder.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105126859A (en) * | 2015-09-20 | 2015-12-09 | 桂林理工大学 | Photocatalyst Sr3Li3Fe2Sb5O20 with visible light response performance and preparation method of photocatalyst Sr3Li3Fe2Sb5O20 |
CN105251501A (en) * | 2015-11-19 | 2016-01-20 | 桂林理工大学 | Visible-light responding photocatalyst Li4Sm2NiTiO8 and preparation method thereof |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3954956A (en) * | 1973-12-14 | 1976-05-04 | E. I. Du Pont De Nemours And Company | Ternary oxides with the cubic KSbO3 crystal structure |
SU1109367A1 (en) * | 1981-12-03 | 1984-08-23 | Ордена Трудового Красного Знамени Институт Нефтехимических Процессов Им.Акад.Ю.Г.Мамедалиева | Process for preparing c9-c14 monoolefins |
CN102205247A (en) * | 2011-03-24 | 2011-10-05 | 桂林理工大学 | Composite oxide photocatalyst LiCuNb3-xTaxO9 with visible light response and preparation method thereof |
CN103480383A (en) * | 2013-10-12 | 2014-01-01 | 桂林理工大学 | Visible-light-responsive photocatalyst Sr2CuBi2O6 and preparation method thereof |
CN103480361A (en) * | 2013-10-12 | 2014-01-01 | 桂林理工大学 | Visible-light-responsive photocatalyst K2MoV2O9 and preparation method thereof |
CN103985851A (en) * | 2014-05-28 | 2014-08-13 | 武汉大学 | Sodium ion battery anode material and sodium iron battery comprising anode material |
CN104205439A (en) * | 2012-03-23 | 2014-12-10 | 法拉典有限公司 | Metallate electrodes |
CN104261816A (en) * | 2014-09-27 | 2015-01-07 | 桂林理工大学 | Low dielectric constant microwave dielectric ceramic NaBi2Sb3O11 capable of being sintered at low temperatures |
-
2015
- 2015-03-06 CN CN201510099374.8A patent/CN104722309B/en active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3954956A (en) * | 1973-12-14 | 1976-05-04 | E. I. Du Pont De Nemours And Company | Ternary oxides with the cubic KSbO3 crystal structure |
SU1109367A1 (en) * | 1981-12-03 | 1984-08-23 | Ордена Трудового Красного Знамени Институт Нефтехимических Процессов Им.Акад.Ю.Г.Мамедалиева | Process for preparing c9-c14 monoolefins |
CN102205247A (en) * | 2011-03-24 | 2011-10-05 | 桂林理工大学 | Composite oxide photocatalyst LiCuNb3-xTaxO9 with visible light response and preparation method thereof |
CN104205439A (en) * | 2012-03-23 | 2014-12-10 | 法拉典有限公司 | Metallate electrodes |
CN103480383A (en) * | 2013-10-12 | 2014-01-01 | 桂林理工大学 | Visible-light-responsive photocatalyst Sr2CuBi2O6 and preparation method thereof |
CN103480361A (en) * | 2013-10-12 | 2014-01-01 | 桂林理工大学 | Visible-light-responsive photocatalyst K2MoV2O9 and preparation method thereof |
CN103985851A (en) * | 2014-05-28 | 2014-08-13 | 武汉大学 | Sodium ion battery anode material and sodium iron battery comprising anode material |
CN104261816A (en) * | 2014-09-27 | 2015-01-07 | 桂林理工大学 | Low dielectric constant microwave dielectric ceramic NaBi2Sb3O11 capable of being sintered at low temperatures |
Non-Patent Citations (1)
Title |
---|
J.R.GANARRI ET AL.: "The Chemical Bonds in MeSb204 (Me=Mn,Ni,Fe,Zn)lsomorphous Compounds: Thermal Expansion,Force Constants, Energies", 《JOURNAL OF SOLID STATE CHEMISTRY》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105126859A (en) * | 2015-09-20 | 2015-12-09 | 桂林理工大学 | Photocatalyst Sr3Li3Fe2Sb5O20 with visible light response performance and preparation method of photocatalyst Sr3Li3Fe2Sb5O20 |
CN105251501A (en) * | 2015-11-19 | 2016-01-20 | 桂林理工大学 | Visible-light responding photocatalyst Li4Sm2NiTiO8 and preparation method thereof |
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