CN104043444A - Visible light responsive photocatalyst Li2ZnW2O8 and preparation method thereof - Google Patents

Visible light responsive photocatalyst Li2ZnW2O8 and preparation method thereof Download PDF

Info

Publication number
CN104043444A
CN104043444A CN201410237915.4A CN201410237915A CN104043444A CN 104043444 A CN104043444 A CN 104043444A CN 201410237915 A CN201410237915 A CN 201410237915A CN 104043444 A CN104043444 A CN 104043444A
Authority
CN
China
Prior art keywords
visible light
preparation
znw
photochemical catalyst
photocatalyst
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201410237915.4A
Other languages
Chinese (zh)
Inventor
唐莹
李洁
方亮
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guilin University of Technology
Original Assignee
Guilin University of Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guilin University of Technology filed Critical Guilin University of Technology
Priority to CN201410237915.4A priority Critical patent/CN104043444A/en
Publication of CN104043444A publication Critical patent/CN104043444A/en
Pending legal-status Critical Current

Links

Landscapes

  • Catalysts (AREA)

Abstract

The invention discloses a visible light responsive photocatalyst Li2ZnW2O8 and a preparation method thereof. The chemical composition formula of the photocatalyst is Li2ZnW2O8. The invention also discloses a preparation method of the material. The photocatalyst obtained by the invention has the advantages of wide spectral response range, high light conversion efficiency, good stability and the like, and can decompose harmful chemical substances and organic biomasses and kill bacteria under visible light irradiation. In addition, the visible light responsive photocatalyst has the characteristics of simple preparation method, low synthesis temperature and low cost, thus being suitable for industrial production and application.

Description

Visible light-responded photocatalyst Li 2znW 2o 8and preparation method thereof
Technical field
The present invention relates to a kind of visible light-responded photocatalyst Li 2znW 2o 8and 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 and be realize sustainable development, improve people's living standard and safeguard national security in the urgent need to.
From phase late 1970s, people proposed to utilize in photochemical catalyst decomposition water and atmosphere in the organic matter such as agricultural chemicals 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 the photon having absorbed higher than its band-gap energy, hole and electronics are generated, these holes and electronics carry out respectively oxidation reaction and reduction reaction, 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), utilize titanium dioxide to decompose the organic matter such as agricultural chemicals and odorant in water and in atmosphere, but 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 have a local work of uviol lamp, almost can not utilize visible ray, 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.Irradiate near sunshine medium wavelength visible light intensity maximum 500nm to earth's surface, wavelength is that the energy of the visible region of 400nm ~ 750nm is approximately 43% of sunshine gross energy, so for efficient utilization, the R and D of bismuth series photocatalyst have obtained a series of great achievements, and bismuthous compound is as BiVO 4, Bi 2moO 6, Bi 2mo 2o 9, Bi 2mo 3o 12and Bi 2wO 4be reported in and under visible ray, there is good absorption.A series of niobiums (tantalum) hydrochlorate photochemical catalyst is because the photocatalytic activity having compared with high is widely studied.For example, 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 thering is good photocatalysis performance.
Although photocatalysis research has been carried out the several years, but at present report to have visible light-responded photochemical catalyst kind still very limited, still exist that light conversion efficiency is low, poor stability and the problem such as spectral response range is narrow, be very necessary so research and develop the new visible light-responded high efficiency photocatalyst that has.We are to synthetic noval chemical compound Li in research 2znW 2o 8carry out Photocatalytic Performance Study, found that Li 2znW 2o 8band gap be 2.1eV, there is excellent visible light-responded photocatalysis performance.
 
Summary of the invention
The object of this invention is to provide a kind of visible light-responded photocatalyst Li that has 2znW 2o 8and preparation method thereof.
The chemical composition general formula with visible light-responded photochemical catalyst the present invention relates to is: Li 2znW 2o 8.
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, ZnO and WO 3, by Li 2znW 2o 8chemical formula weigh batching.
(2) raw material step (1) being prepared mixes, and puts into ball grinder, adds zirconia ball and distilled water, and ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) being mixed is 600 ~ 620 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then by ball mill pulverizing means, average diameter of particles diminished, and lower than 2 μ m, obtains Li 2znW 2o 8powder.
Of the present invention beneficial effect: the spectral response range of the photochemical catalyst that the present invention obtains is wide that the high and good stability of light conversion efficiency has the effect of decomposing harmful chemical, organic-biological matter and sterilization under radiation of visible light; 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, the composite oxides in order to obtain using in the present invention, first use solid-phase synthesis to prepare powder, various oxides or carbonate as raw material measured than mixing according to target constitutional chemistry, more synthetic in air atmosphere under normal pressure.
2, in order effectively to 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.The oxide powder of preparing with solid-phase synthesis, its particle is compared with large and surface area is less, but can particle diameter be diminished by ball mill pulverizing means.
3, photocatalysis experiment of the present invention is using methyl orange as simulation organic pollution, and its concentration is 20mg/L; Photocatalyst Li 2znW 2o 8addition be 1g/L; Light source uses the xenon lamp of 300W, and the vessel that reactive tank uses pyrex to make, obtain by wave filter the light that wavelength is greater than 420nm long wavelength, then light irradiation catalyst; Catalysis time is set as 60 minutes.
Embodiment 1:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, ZnO and WO 3, by Li 2znW 2o 8chemical formula weigh batching.
(2) raw material step (1) being prepared mixes, and puts into ball grinder, adds zirconia ball and distilled water, and ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) being mixed is 600 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then by ball mill pulverizing means, average diameter of particles diminished, and lower than 2 μ m, obtains Li 2znW 2o 8powder.
Prepared photochemical catalyst, is greater than at wavelength under the radiation of visible light of 420nm, methyl orange clearance is reached to 98.7% in 60 minutes.
Embodiment 2:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, ZnO and WO 3, by Li 2znW 2o 8chemical formula weigh batching.
(2) raw material step (1) being prepared mixes, and puts into ball grinder, adds zirconia ball and distilled water, and ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) being mixed is 610 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then by ball mill pulverizing means, average diameter of particles diminished, and lower than 2 μ m, obtains Li 2znW 2o 8powder.
Prepared photochemical catalyst, is greater than at wavelength under the radiation of visible light of 420nm, methyl orange clearance is reached to 99.5% in 60 minutes.
Embodiment 3:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, ZnO and WO 3, by Li 2znW 2o 8chemical formula weigh batching.
(2) raw material step (1) being prepared mixes, and puts into ball grinder, adds zirconia ball and distilled water, and ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves.
(3) powder step (2) being mixed is 620 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then by ball mill pulverizing means, average diameter of particles diminished, and lower than 2 μ m, obtains Li 2znW 2o 8powder.
Prepared photochemical catalyst, is greater than at wavelength under the radiation of visible light of 420nm, and 60min reaches 98.4% 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 with the form of film.

Claims (1)

1. a visible light-responded photochemical catalyst, is characterized in that the chemical constitution formula of described photochemical catalyst is: Li 2znW 2o 8;
Preparation method's concrete steps of described photochemical catalyst are:
(1) by 99.9% analytically pure chemical raw material Li 2cO 3, ZnO and and WO 3, by Li 2znW 2o 8chemical formula weigh batching;
(2) raw material step (1) being prepared mixes, and puts into ball grinder, adds zirconia ball and distilled water, and ball milling 8 hours, is mixed and finely ground, and takes out and dries, and crosses 200 mesh sieves;
(3) powder step (2) being mixed is 600 ~ 620 DEG C of pre-burnings, and is incubated 6 hours, naturally cools to room temperature, then makes average diameter of particles lower than 2 μ m by ball mill pulverizing means, obtains Li 2znW 2o 8powder.
CN201410237915.4A 2014-06-02 2014-06-02 Visible light responsive photocatalyst Li2ZnW2O8 and preparation method thereof Pending CN104043444A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410237915.4A CN104043444A (en) 2014-06-02 2014-06-02 Visible light responsive photocatalyst Li2ZnW2O8 and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410237915.4A CN104043444A (en) 2014-06-02 2014-06-02 Visible light responsive photocatalyst Li2ZnW2O8 and preparation method thereof

Publications (1)

Publication Number Publication Date
CN104043444A true CN104043444A (en) 2014-09-17

Family

ID=51497133

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410237915.4A Pending CN104043444A (en) 2014-06-02 2014-06-02 Visible light responsive photocatalyst Li2ZnW2O8 and preparation method thereof

Country Status (1)

Country Link
CN (1) CN104043444A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104226302A (en) * 2014-09-20 2014-12-24 桂林理工大学 Visible-light response photocatalyst Nd2ZnW3O13 and preparation method thereof
CN104307510A (en) * 2014-10-26 2015-01-28 桂林理工大学 Visible light responding photocatalyst Li4SnWO7 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
CN104667942A (en) * 2015-02-26 2015-06-03 桂林理工大学 Photocatalyst LiCuNb5O14 with visible light response and preparation method thereof
CN105268426A (en) * 2015-10-10 2016-01-27 桂林理工大学 Visible light responsive photocatalyst Li3Zn2Nd5O11 and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103111283A (en) * 2013-03-24 2013-05-22 桂林理工大学 Visible-light responsive oxide photocatalyst Li2M2Mo3O12 and preparation method thereof
CN103191719A (en) * 2013-04-01 2013-07-10 桂林理工大学 Visible-light-responded photocatalyst Li4M5O17 and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103111283A (en) * 2013-03-24 2013-05-22 桂林理工大学 Visible-light responsive oxide photocatalyst Li2M2Mo3O12 and preparation method thereof
CN103191719A (en) * 2013-04-01 2013-07-10 桂林理工大学 Visible-light-responded photocatalyst Li4M5O17 and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104226302A (en) * 2014-09-20 2014-12-24 桂林理工大学 Visible-light response photocatalyst Nd2ZnW3O13 and preparation method thereof
CN104307510A (en) * 2014-10-26 2015-01-28 桂林理工大学 Visible light responding photocatalyst Li4SnWO7 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
CN104667942A (en) * 2015-02-26 2015-06-03 桂林理工大学 Photocatalyst LiCuNb5O14 with visible light response and preparation method thereof
CN105268426A (en) * 2015-10-10 2016-01-27 桂林理工大学 Visible light responsive photocatalyst Li3Zn2Nd5O11 and preparation method thereof

Similar Documents

Publication Publication Date Title
CN103877968B (en) Visible light-responded photocatalyst Li3Nb3Si2O13And preparation method thereof
CN104069866A (en) Photocatalyst LiCu2V3O10 in response to visible light and preparation method thereof
CN104190398A (en) Visible light responding photocatalyst Bi2Sm4Ti5O19 and preparation method thereof
CN104069865A (en) Photocatalyst LiFe2V3O11 in response to visible light and preparation method thereof
CN104368330A (en) Photocatalyst Li2Bi3Nb7O23 with visible light response and preparation method thereof
CN103521210A (en) Photocatalyst Bi3Sb3Zn2O14 with visible light response
CN104043444A (en) Visible light responsive photocatalyst Li2ZnW2O8 and preparation method thereof
CN103521213A (en) Photocatalyst LiLaV2O7 with visible-light response and preparation method thereof
CN104190400A (en) Visible light responding photocatalyst Ca3La4V2O14 and preparation method thereof
CN104258844A (en) Photocatalyst YVWO7 capable of responding visible light and preparation method of photocatalyst YVWO7
CN104190404B (en) Visible light-responded photochemical catalyst SmNbMo2O10And preparation method thereof
CN103551163A (en) Visible-light response photocatalyst Bi2Fe2W3O15 as well as preparation method thereof
CN103480364A (en) Photocatalyst La responsive to visible light7Nb3W4O30And method for preparing the same
CN103877967B (en) Visible light-responded photocatalyst Li 3nb 3bi 2o 12and preparation method thereof
CN104324725A (en) Visible-light response light catalyst Li2Si3Ta8O27 and preparation method thereof
CN104069849A (en) Photocatalyst Li3Ti2VO8 in response to visible light and preparation method thereof
CN104001530B (en) Visible light-responded photocatalyst Li VP2O8And preparation method thereof
CN103418370B (en) Visible light-responded photochemical catalyst Ca3WO6And preparation method thereof
CN104001527A (en) Visible-light-responsive photocatalyst Li3Ti2PO8 and preparation method thereof
CN104492419A (en) Visible light responding photocatalyst LiBi3B3O11 and preparation method thereof
CN104307509A (en) Visible light responding photocatalyst Li3LaWO6 and preparation method thereof
CN104307532A (en) Visible-light response photocatalyst CuSnW2O9 and preparation method thereof
CN104324719A (en) Visible light responding photocatalyst and preparation method thereof
CN104190407A (en) Visible light responding photocatalyst SrBi2W6O22 and preparation method thereof
CN104069850A (en) Photocatalyst LiTi2V3O12 in response to visible light and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20140917