CN103433030B - Visible light-responded tungstates photochemical catalyst Sr 2wO 5and preparation method thereof - Google Patents
Visible light-responded tungstates photochemical catalyst Sr 2wO 5and preparation method thereof Download PDFInfo
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- CN103433030B CN103433030B CN201310399558.7A CN201310399558A CN103433030B CN 103433030 B CN103433030 B CN 103433030B CN 201310399558 A CN201310399558 A CN 201310399558A CN 103433030 B CN103433030 B CN 103433030B
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- Prior art keywords
- photochemical catalyst
- preparation
- visible light
- tungstates
- responded
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- 239000003054 catalyst Substances 0.000 title claims abstract description 26
- 238000002360 preparation method Methods 0.000 title claims abstract description 12
- 239000000126 substance Substances 0.000 claims abstract description 12
- 239000000843 powder Substances 0.000 claims description 13
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000000498 ball milling Methods 0.000 claims description 5
- 239000013064 chemical raw material Substances 0.000 claims description 5
- 230000003292 diminished effect Effects 0.000 claims description 5
- 230000000694 effects Effects 0.000 abstract description 3
- 230000003197 catalytic effect Effects 0.000 abstract description 2
- 238000005286 illumination Methods 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract description 2
- 230000001699 photocatalysis Effects 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- 238000007146 photocatalysis Methods 0.000 description 5
- 239000011941 photocatalyst Substances 0.000 description 5
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 4
- 229940012189 methyl orange Drugs 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 238000010532 solid phase synthesis reaction Methods 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- VEUKJXRCHYAIAW-UHFFFAOYSA-N [Nb].[K] Chemical compound [Nb].[K] VEUKJXRCHYAIAW-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000001621 bismuth Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- RHDUVDHGVHBHCL-UHFFFAOYSA-N niobium tantalum Chemical class [Nb].[Ta] RHDUVDHGVHBHCL-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
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- Catalysts (AREA)
Abstract
The invention discloses a kind of visible light-responded photochemical catalyst Sr
2wO
5and preparation method thereof.The chemical constitution formula of this photochemical catalyst is Sr
2wO
5.The invention also discloses the preparation method of above-mentioned material.Preparation method of the present invention is simple, cost is low, and the photochemical catalyst of preparation has excellent catalytic performance, has the effect of decomposing harmful chemical under visible light illumination, and good stability, have a good application prospect.
Description
Technical field
The present invention relates to a kind of visible light-responded photochemical catalyst Sr
2wO
5and 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 or 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.
Although photocatalysis research has carried out the several years, but at present report to have visible light-responded photochemical catalyst kind still very limited, still also exist that light conversion efficiency is low, poor stability and the problem such as spectrum respective range is narrow, so it is very necessary for researching and developing the new visible light-responded high efficiency photocatalyst that has.We are to Ba
2wO
5, Sr
2wO
5and Ca
2wO
5carry out Photocatalytic Performance Study Deng tungstates, found that Sr
2wO
5there is excellent visible light-responded photocatalysis performance, but Ba
2wO
5and Ca
2wO
5but not there is visible light-responded photocatalysis performance.
Summary of the invention
The object of this invention is to provide and a kind of there is visible light-responded photochemical catalyst Sr
2wO
5and preparation method thereof.
The chemical constitution formula with visible light-responded photochemical catalyst that the present invention relates to is: Sr
2wO
5.
Preparation method's concrete steps of above-mentioned visible light-responded photochemical catalyst are:
(1) by 99.9% analytically pure chemical raw material SrCO
3and WO
3, by Sr
2wO
5chemical formula 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 1050 ~ 1100 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then pulverizes means by ball mill and particle diameter is diminished, lower than 2 μm, namely obtain Sr
2wO
5powder.
Preparation method of the present invention is simple, cost is low, and the photochemical catalyst of preparation has excellent catalytic performance, has the effect of decomposing harmful chemical, organic-biological matter and sterilization under visible light illumination.
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 Sr
2wO
5addition 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 long wavelength, then irradiate photochemical catalyst by wave filter; Catalysis time is set as 120 minutes.
Embodiment 1:
(1) by 99.9% analytically pure chemical raw material SrCO
3and WO
3, by Sr
2wO
5chemical formula 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 1050 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then pulverizes means by ball mill and particle diameter is diminished, lower than 2 μm, namely obtain Sr
2wO
5powder.
Prepared photochemical catalyst, under being greater than the radiation of visible light of 420nm, reaches 97.9% to methyl orange clearance in 120 minutes at wavelength.
Embodiment 2:
(1) by 99.9% analytically pure chemical raw material SrCO
3and WO
3, by Sr
2wO
5chemical formula 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 1075 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then pulverizes means by ball mill and particle diameter is diminished, lower than 2 μm, namely obtain Sr
2wO
5powder.
Prepared photochemical catalyst, under being greater than the radiation of visible light of 420nm, reaches 98.9% to methyl orange clearance in 120 minutes at wavelength.
Embodiment 3:
(1) by 99.9% analytically pure chemical raw material SrCO
3and WO
3, by Sr
2wO
5chemical formula 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 1100 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then pulverizes means by ball mill and particle diameter is diminished, lower than 2 μm, namely obtain Sr
2wO
5powder.
Prepared photochemical catalyst, be greater than the radiation of visible light of 420nm at wavelength under, 120min reaches 98.6% 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. tungstates is as an application for visible light-responded photochemical catalyst, it is characterized in that the chemical constitution formula of described tungstates is: Sr
2wO
5;
Preparation method's concrete steps of described tungstates are:
(1) by 99.9% analytically pure chemical raw material SrCO
3and WO
3, by Sr
2wO
5chemical formula 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 1050 ~ 1100 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then pulverizes means by ball mill and particle diameter is diminished, lower than 2 μm, namely obtain Sr
2wO
5powder.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310399558.7A CN103433030B (en) | 2013-09-05 | 2013-09-05 | Visible light-responded tungstates photochemical catalyst Sr 2wO 5and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310399558.7A CN103433030B (en) | 2013-09-05 | 2013-09-05 | Visible light-responded tungstates photochemical catalyst Sr 2wO 5and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103433030A CN103433030A (en) | 2013-12-11 |
| CN103433030B true CN103433030B (en) | 2016-01-13 |
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ID=49686799
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|---|---|---|---|
| CN201310399558.7A Expired - Fee Related CN103433030B (en) | 2013-09-05 | 2013-09-05 | Visible light-responded tungstates photochemical catalyst Sr 2wO 5and preparation method thereof |
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| Country | Link |
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Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104190407B (en) * | 2014-09-24 | 2016-08-24 | 桂林理工大学 | Visible light-responded photocatalyst SrBi2w6o22and preparation method thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102372305A (en) * | 2010-08-13 | 2012-03-14 | 范晓星 | Mesoporous tungstate photocatalysis material and preparation method thereof |
| CN103111288A (en) * | 2013-03-24 | 2013-05-22 | 桂林理工大学 | Visible-light responsive tungstenic composite oxide photocatalyst Li2WO4 and preparation method thereof |
-
2013
- 2013-09-05 CN CN201310399558.7A patent/CN103433030B/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102372305A (en) * | 2010-08-13 | 2012-03-14 | 范晓星 | Mesoporous tungstate photocatalysis material and preparation method thereof |
| CN103111288A (en) * | 2013-03-24 | 2013-05-22 | 桂林理工大学 | Visible-light responsive tungstenic composite oxide photocatalyst Li2WO4 and preparation method thereof |
Non-Patent Citations (2)
| Title |
|---|
| Emissions and photocatalytic selectivity of SrWO4: Ln3+(Eu3+,Tb3+,Sm3+ and Dy3+) prepared by a supersonic microwave co-assistance method;Yuhui Zheng et al;《Photochemical & Photobiological Sciences》;20120710;第11卷;第1567-1574页 * |
| 钨酸锶微粉的阳极氧化法制备及其光催化性能研究;李旭云等;《中国陶瓷》;20130531;第49卷(第5期);第40-42页 * |
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