CN104437465A - Visible light responded photocatalyst LiNb2BO7 and preparation method thereof - Google Patents

Visible light responded photocatalyst LiNb2BO7 and preparation method thereof Download PDF

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CN104437465A
CN104437465A CN201410825542.2A CN201410825542A CN104437465A CN 104437465 A CN104437465 A CN 104437465A CN 201410825542 A CN201410825542 A CN 201410825542A CN 104437465 A CN104437465 A CN 104437465A
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photocatalyst
visible light
preparation
photochemical catalyst
linb
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CN104437465B (en
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唐莹
苏和平
蒋雪雯
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Guangzhou Boyi Intellectual Property Operation Co ltd
Shandong Xingqiang Chemical Industry Technology Research Institute Co ltd
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Guilin University of Technology
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Abstract

The invention discloses a visible light responded photocatalyst LiNb2BO7 and the preparation method thereof. The chemical constitution formula of the photocatalyst is LiNb2BO7. The invention further discloses a preparation method of the aforementioned material. The obtained photocatalyst has the advantages of wide spectral response range, high light conversion efficiency, good stability, and the like. Under the irradiation of visible light, the photocatalyst has effects of resolving harmful chemical substances, organic biomass, and sterilization; additionally, the preparation method is simple, the synthesizing temperature is low, and the photocatalyst is applicable to industrial production and application.

Description

Visible light-responded photocatalyst Li Nb 2bO 7and preparation method thereof
Technical field
The present invention relates to a kind of visible light-responded photocatalyst Li Nb 2bO 7and 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 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 LiNb 2bO 7, LiTa 2bO 7, LiV 2bO 7sample carried out Photocatalytic Performance Study.Found that LiNb 2bO 7for semiconductor, band gap is 2.55eV, has excellent visible light-responded photocatalysis performance; LiTa 2bO 7band gap width is greater than 3.2eV, can only show activity under ultraviolet irradiation, and LiV 2bO 7sample is insulator, can not show activity under ultraviolet irradiation.
 
Summary of the invention
The object of this invention is to provide and a kind of there is visible light-responded photocatalyst Li Nb 2bO 7and preparation method thereof.
The chemical constitution formula with visible light-responded photochemical catalyst that the present invention relates to is: LiNb 2bO 7.
Preparation method's concrete steps of above-mentioned visible light-responded photochemical catalyst are:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, Nb 2o 5and H 3bO 3starting powder press LiNb 2bO 7composition 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 730 ~ 780 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 LiNb 2bO 7powder.
The spectral response range of the photochemical catalyst that the present invention obtains is wide, 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; Photocatalyst Li Nb 2bO 7addition 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 Li 2cO 3, Nb 2o 5and H 3bO 3starting powder press LiNb 2bO 7composition 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 730 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 LiNb 2bO 7powder.
Prepared photochemical catalyst, under being greater than the radiation of visible light of 420nm, reaches 97.9% to methyl orange clearance in 60 minutes at wavelength.
Embodiment 2:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, Nb 2o 5and H 3bO 3starting powder press LiNb 2bO 7composition 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 760 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 LiNb 2bO 7powder.
Prepared photochemical catalyst, under being greater than the radiation of visible light of 420nm, reaches 98.6% to methyl orange clearance in 60 minutes at wavelength.
Embodiment 3:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, Nb 2o 5and H 3bO 3starting powder press LiNb 2bO 7composition 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 780 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 LiNb 2bO 7powder.
Prepared photochemical catalyst, be greater than the radiation of visible light of 420nm at wavelength under, 60min reaches 97.8% 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 LiNb 2bO 7;
Preparation method's concrete steps of described photochemical catalyst are:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, Nb 2o 5and H 3bO 3starting powder press LiNb 2bO 7composition 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 730 ~ 780 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 LiNb 2bO 7powder.
CN201410825542.2A 2014-12-28 2014-12-28 Visible light-responded photocatalyst Li Nb2bO7and preparation method thereof Active CN104437465B (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106000388A (en) * 2016-07-23 2016-10-12 桂林理工大学 Visible light response photocatalyst LiB3Sn2O9 and method for preparing same
CN106040219A (en) * 2016-06-27 2016-10-26 桂林理工大学 Broadband high-efficiency visible light response photocatalyst LiBSnO4 and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1736583A (en) * 2005-08-18 2006-02-22 清华大学 Synthesis method of boron-doped nanometer oxide and use thereof
CN101780405A (en) * 2009-01-20 2010-07-21 华东交通大学 Preparation method of boron-doped titanium dioxide visible-light responsive photocatalyst
CN101947440A (en) * 2010-10-29 2011-01-19 哈尔滨工业大学 Preparation method of boron-doped modified TiO2 photocatalyst
CN103877967A (en) * 2014-04-07 2014-06-25 桂林理工大学 Visible-light response photocatalyst Li3Nb3Bi2O12 and preparation method thereof
CN103877968A (en) * 2014-04-07 2014-06-25 桂林理工大学 Visible-light response photocatalyst Li3Nb3Si2O13 and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1736583A (en) * 2005-08-18 2006-02-22 清华大学 Synthesis method of boron-doped nanometer oxide and use thereof
CN101780405A (en) * 2009-01-20 2010-07-21 华东交通大学 Preparation method of boron-doped titanium dioxide visible-light responsive photocatalyst
CN101947440A (en) * 2010-10-29 2011-01-19 哈尔滨工业大学 Preparation method of boron-doped modified TiO2 photocatalyst
CN103877967A (en) * 2014-04-07 2014-06-25 桂林理工大学 Visible-light response photocatalyst Li3Nb3Bi2O12 and preparation method thereof
CN103877968A (en) * 2014-04-07 2014-06-25 桂林理工大学 Visible-light response photocatalyst Li3Nb3Si2O13 and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106040219A (en) * 2016-06-27 2016-10-26 桂林理工大学 Broadband high-efficiency visible light response photocatalyst LiBSnO4 and preparation method thereof
CN106000388A (en) * 2016-07-23 2016-10-12 桂林理工大学 Visible light response photocatalyst LiB3Sn2O9 and method for preparing same

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