CN104646019B - Visible light-responded photocatalyst Li Cu3nbWO9and preparation method thereof - Google Patents

Visible light-responded photocatalyst Li Cu3nbWO9and preparation method thereof Download PDF

Info

Publication number
CN104646019B
CN104646019B CN201510088364.4A CN201510088364A CN104646019B CN 104646019 B CN104646019 B CN 104646019B CN 201510088364 A CN201510088364 A CN 201510088364A CN 104646019 B CN104646019 B CN 104646019B
Authority
CN
China
Prior art keywords
nbwo
licu
photochemical catalyst
visible light
preparation
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.)
Active
Application number
CN201510088364.4A
Other languages
Chinese (zh)
Other versions
CN104646019A (en
Inventor
方维双
苏和平
李洁
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.)
Guangzhou Boyi Intellectual Property Operation Co ltd
Shandong Xingqiang Chemical Industry Technology Research Institute Co ltd
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 CN201510088364.4A priority Critical patent/CN104646019B/en
Publication of CN104646019A publication Critical patent/CN104646019A/en
Application granted granted Critical
Publication of CN104646019B publication Critical patent/CN104646019B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Catalysts (AREA)

Abstract

The invention discloses the visible light responsive photocatalyst LiCu of a kind of high-efficient wide-frequency3NbWO9And preparation method thereof.The chemical constitution formula of this photochemical catalyst is LiCu3NbWO9.The invention also discloses the preparation method of above-mentioned material.The photochemical catalyst that the present invention obtains has the advantages such as spectral response range width, 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 industrial production and application.

Description

Visible light-responded photochemical catalystLiCu3NbWO9And preparation method thereof
Technical field
The present invention relates to a kind of visible light-responded photocatalyst Li Cu3NbWO9And 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 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 be photochemical catalyst 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.Photochemical catalyst has many kinds, and the most most representative is titanium dioxide (TiO2), utilize titanium dioxide that the organic matters such as the agricultural chemicals 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 photochemical catalyst practicality in decomposing harmful substances, it is indispensable for utilizing sunlight as light source.Irradiate the sunshine 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 sunshine 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 compound 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 photochemical catalyst 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, but in visible-range, its intrinsic photocatalytic effect is the most weak or does not has activity.
Although photocatalysis research has been carried out the several years, major part of exploring and develop to visible light-responded photochemical catalyst is the summary of experience drawn by great many of experiments at present, the most also cannot be from the crystal structure of compound, composition, its photocatalysis performance is predicted in the physicochemical properties such as molecular weight, therefore at present report to have visible light-responded photochemical catalyst kind the most 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 succeeded all the time, which greatly limits extensively application and the development of photochemical catalyst.We are to consisting of LiMg3NbWO9、LiZn3NbWO9And LiCu3NbWO9Sample carried out Photocatalytic Performance Study.Found that LiCu3NbWO9Band gap is 2.64eV, has the visible light-responded photocatalysis performance of excellence; LiMg3NbWO9And LiZn3NbWO9For insulator, under ultraviolet irradiation, the most do not show activity.
Summary of the invention
It is an object of the invention to provide and a kind of there is visible light-responded photocatalyst Li Cu3NbWO9And preparation method thereof.
The chemical constitution formula with visible light-responded photochemical catalyst that the present invention relates to is: LiCu3NbWO9
The preparation method of above-mentioned visible light-responded photochemical catalyst concretely comprises the following steps:
(1) by 99.9% analytically pure chemical raw material Li2CO3、CuO、Nb2O5And WO3Starting powder press LiCu3NbWO9Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and absolute ethyl alcohol, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) powder step (2) mixed is 1000 ~ 1050 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 diminish, less than 2 μm, i.e. obtains LiCu3NbWO9Powder.
Advantages of the present invention: LiCu3NbWO9The visible light-responded wide frequency range of photochemical catalyst, 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 industrial 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 photochemical catalyst in the present invention preferably in micron level, even nano particle, 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 Li Cu3NbWO9Addition 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 by wave filter, then irradiates photochemical catalyst;Catalysis time is set as 60 minutes.
Embodiment 1:
(1) by 99.9% analytically pure chemical raw material Li2CO3、CuO、Nb2O5And WO3Starting powder press LiCu3NbWO9Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and absolute ethyl alcohol, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) powder step (2) mixed is 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 diminish, less than 2 μm, i.e. obtains LiCu3NbWO9Powder.
Prepared photochemical catalyst, under the wavelength radiation of visible light more than 420nm, reaches 97.9% to methyl orange clearance in 60 minutes.
Embodiment 2:
(1) by 99.9% analytically pure chemical raw material Li2CO3、CuO、Nb2O5And WO3Starting powder press LiCu3NbWO9Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and absolute ethyl alcohol, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) powder step (2) mixed is 1020 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 diminish, less than 2 μm, i.e. obtains LiCu3NbWO9Powder.
Prepared photochemical catalyst, under the wavelength radiation of visible light more than 420nm, reaches 98.9% to methyl orange clearance in 60 minutes.
Embodiment 3:
(1) by 99.9% analytically pure chemical raw material Li2CO3、CuO、Nb2O5And WO3Starting powder press LiCu3NbWO9Composition weigh dispensing.
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and absolute ethyl alcohol, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves.
(3) powder step (2) mixed is 1050 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 diminish, less than 2 μm, i.e. obtains LiCu3NbWO9Powder.
Prepared photochemical catalyst, under the wavelength radiation of visible light more than 420nm, 60min reaches 98.6% 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 photochemical catalyst can be carried on matrix surface in the form of a film.

Claims (1)

1. a visible light-responded photochemical catalyst, it is characterised in that the chemical constitution formula of described photochemical catalyst is LiCu3NbWO9
The preparation method of described photochemical catalyst concretely comprises the following steps:
(1) by 99.9% analytically pure chemical raw material Li2CO3、CuO、Nb2O5And WO3Starting powder press LiCu3NbWO9Composition weigh dispensing;
(2) raw material mixing step (1) prepared, puts in ball grinder, adds zirconia ball and absolute ethyl alcohol, ball milling 8 hours, be mixed and finely ground, take out and dry, cross 200 mesh sieves;
(3) powder step (2) mixed is 1000 ~ 1050 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 be less than 2 μm, i.e. obtains LiCu3NbWO9Powder.
CN201510088364.4A 2015-02-26 2015-02-26 Visible light-responded photocatalyst Li Cu3nbWO9and preparation method thereof Active CN104646019B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510088364.4A CN104646019B (en) 2015-02-26 2015-02-26 Visible light-responded photocatalyst Li Cu3nbWO9and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510088364.4A CN104646019B (en) 2015-02-26 2015-02-26 Visible light-responded photocatalyst Li Cu3nbWO9and preparation method thereof

Publications (2)

Publication Number Publication Date
CN104646019A CN104646019A (en) 2015-05-27
CN104646019B true CN104646019B (en) 2016-08-24

Family

ID=53237951

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510088364.4A Active CN104646019B (en) 2015-02-26 2015-02-26 Visible light-responded photocatalyst Li Cu3nbWO9and preparation method thereof

Country Status (1)

Country Link
CN (1) CN104646019B (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103433052A (en) * 2013-09-05 2013-12-11 桂林理工大学 Visible-light-responsive photocatalyst Ba2WCuO6 and preparation method thereofore
CN103433048A (en) * 2013-09-09 2013-12-11 桂林理工大学 Visible-light-responsive photocatalyst Cu3Nb2O8 and preparation method thereof
CN103480364A (en) * 2013-10-14 2014-01-01 桂林理工大学 Photocatalyst La responsive to visible light7Nb3W4O30And method for preparing the same
CN103495423A (en) * 2013-09-23 2014-01-08 桂林理工大学 Visible-light response wolframate photocatalyst Li2CuW2O8 and preparation method thereof
CN104307532A (en) * 2014-10-13 2015-01-28 桂林理工大学 Visible-light response photocatalyst CuSnW2O9 and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103433052A (en) * 2013-09-05 2013-12-11 桂林理工大学 Visible-light-responsive photocatalyst Ba2WCuO6 and preparation method thereofore
CN103433048A (en) * 2013-09-09 2013-12-11 桂林理工大学 Visible-light-responsive photocatalyst Cu3Nb2O8 and preparation method thereof
CN103495423A (en) * 2013-09-23 2014-01-08 桂林理工大学 Visible-light response wolframate photocatalyst Li2CuW2O8 and preparation method thereof
CN103480364A (en) * 2013-10-14 2014-01-01 桂林理工大学 Photocatalyst La responsive to visible light7Nb3W4O30And method for preparing the same
CN104307532A (en) * 2014-10-13 2015-01-28 桂林理工大学 Visible-light response photocatalyst CuSnW2O9 and preparation method thereof

Also Published As

Publication number Publication date
CN104646019A (en) 2015-05-27

Similar Documents

Publication Publication Date Title
CN104368330B (en) Visible light-responded photocatalyst Li2bi3nb7o23and preparation method thereof
CN104437503B (en) Visible light-responded photocatalyst Li2cu2si4o11and preparation method thereof
CN104667905A (en) Photocatalyst LiSm2NbO6 with visible light response and preparation method thereof
CN104190400B (en) Visible light-responded photocatalyst Ca3La4V2O14And preparation method thereof
CN104324725B (en) Visible light-responded photocatalyst Li2si3ta8o27and preparation method thereof
CN104275199B (en) A kind of visible light-responded fluorine-containing photochemical catalyst and preparation method thereof
CN104069849B (en) Visible light-responded photocatalyst Li3ti2vO8and preparation method thereof
CN105688887A (en) Visible-light response photocatalyst BaLi4Ge5O13 and preparation method thereof
CN104722309B (en) Visible light-responded photochemical catalyst K2ni2sb8o23and preparation method thereof
CN104437465B (en) Visible light-responded photocatalyst Li Nb2bO7and preparation method thereof
CN104492419B (en) Visible light-responded photocatalyst Li Bi3b4o11and preparation method thereof
CN104645992B (en) Visible light-responded photocatalyst Li3cu2bO5and preparation method thereof
CN104275176B (en) Visible light-responded photocatalyst Ca3Nb3V5O23And preparation method thereof
CN104324719B (en) Visible light-responded photocatalyst and preparation method thereof
CN104190407B (en) Visible light-responded photocatalyst SrBi2w6o22and preparation method thereof
CN104437506B (en) Visible light-responded photocatalyst Li2cu4o5and preparation method thereof
CN104437461B (en) Visible light-responded photocatalyst Li3bi5o9and preparation method thereof
CN104525208B (en) Visible light-responded photocatalyst Li Fe2b3o8and preparation method thereof
CN104437507B (en) Visible light-responded photocatalyst Li4cuO3and preparation method thereof
CN104437514B (en) Visible light-responded photocatalyst Co3znFeSbO8and preparation method thereof
CN104399463B (en) Visible light-responded photocatalyst Li Cu2b3o7and preparation method thereof
CN104383908B (en) Visible light-responded photocatalyst InNdMg7o10and preparation method thereof
CN104307506B (en) Visible light-responded photocatalyst CaNb4v2o16and preparation method thereof
CN104190403B (en) Visible light-responded photocatalyst Y3VNb2O12And preparation method thereof
CN104646019B (en) Visible light-responded photocatalyst Li Cu3nbWO9and 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
C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20201210

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: 20201210

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

TR01 Transfer of patent right