CN105689015A - Visible light responded layered titanic acid photocatalyst as well as peroxidation modifying method and application of visible light responded layered titanic acid photocatalyst - Google Patents

Visible light responded layered titanic acid photocatalyst as well as peroxidation modifying method and application of visible light responded layered titanic acid photocatalyst Download PDF

Info

Publication number
CN105689015A
CN105689015A CN201610178898.0A CN201610178898A CN105689015A CN 105689015 A CN105689015 A CN 105689015A CN 201610178898 A CN201610178898 A CN 201610178898A CN 105689015 A CN105689015 A CN 105689015A
Authority
CN
China
Prior art keywords
titanic acid
layered titanic
visible light
responded
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
CN201610178898.0A
Other languages
Chinese (zh)
Inventor
孔新刚
曾超斌
黄剑锋
吴建鹏
殷立雄
欧阳海波
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.)
Shaanxi University of Science and Technology
Original Assignee
Shaanxi University of Science and 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 Shaanxi University of Science and Technology filed Critical Shaanxi University of Science and Technology
Priority to CN201610178898.0A priority Critical patent/CN105689015A/en
Publication of CN105689015A publication Critical patent/CN105689015A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00Regeneration or reactivation of catalysts, in general
    • B01J38/48Liquid treating or treating in liquid phase, e.g. dissolved or suspended
    • B01J38/70Wet oxidation of material submerged in liquid
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86Catalytic processes
    • B01D53/8678Removing components of undefined structure
    • B01D53/8687Organic components
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/063Titanium; Oxides or hydroxides thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/30Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
    • B01J35/39Photocatalytic properties
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/30Treatment of water, waste water, or sewage by irradiation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/207Transition metals
    • B01D2255/20707Titanium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/80Type of catalytic reaction
    • B01D2255/802Photocatalytic
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/30Organic compounds
    • C02F2101/308Dyes; Colorants; Fluorescent agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Environmental & Geological Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Toxicology (AREA)
  • Hydrology & Water Resources (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Water Supply & Treatment (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Catalysts (AREA)

Abstract

The invention discloses a visible light responded layered titanic acid photocatalyst as well as a peroxidation modifying method and application of the visible light responded layered titanic acid photocatalyst, and belongs to the field of photocatalytic materials. The visible light responded layered titanic acid photocatalyst yellow powder is obtained by the following steps: adding layered titanic acid white powder into an H2O2 water solution; after stirring to react, filtering and washing with de-ionized water; drying. Ti-O-O- coordination bonds exist between TiO6 octahedral layers of the prepared visible light responded layered titanic acid photocatalyst. Compared with products of solid-phase high-temperature doping modification and heterogeneous semi-conductive compounding, H2O2 peroxidation modified layered titanic acid has the advantages of rapid modifying speed, simple technical process and easiness of controlling, is suitable for large-batch production and the like. The lot of Ti-O-O- coordination bonds exist between the TiO6 octaheadral layers of the prepared visible light responded layered titanic acid photocatalyst prepared by the method, and the forbidden bandwidth is 2.2eV to 2.5eV; the visible light catalytic activity is stronger than that of commercial titanium dioxide P25, so that the visible light responded layered titanic acid photocatalyst can be widely applied to the aspect of degrading environment pollutants or organic matters.

Description

A kind of visible light-responded layered titanic acid photocatalyst and superoxidized modified methods and applications thereof
Technical field
The invention belongs to field of photocatalytic material, be specifically related to a kind of visible light-responded layered titanic acid photocatalyst and superoxidized modified methods and applications thereof。
Background technology
Metatitanic acid (H due to layer structure1.07Ti1.73O4, H2Ti4O9, H2Ti3O7, H2Ti5O11, H0.67Ti1.83O4Deng) there is open structure, research emphasis is concentrated mainly on stripped laminar metatitanic acid by Chinese scholars, thus synthesizing the derivates nanometer sheet of two-dimensional layer metatitanic acid nanometer sheet or two-dimensional nano titanium dioxide, the material of these two dimensions has the performance of excellence。Owing to the energy gap of layered titanic acid itself is bigger, can only to ultraviolet light response, can not being well applied to photocatalysis field, Most scholars is main or with other quasiconductor composition hetero-junctions, it is applied to photocatalysis, which also limits its application in photocatalysis field。
Oxygen-rich silicon dioxide titanium is found to have good visible light photocatalysis active。(Chem.Commun.2014,50,6923-6926) are current, prepare what the method for oxygen-rich silicon dioxide titanyl obtained mainly by the peroxide xerogel of Heat Treated Titanium。(Adv.Funct.Mater.2011,21,3744-3752) first H2O2Aqueous solution and butyl titanate react the peroxide generating soluble titanium, are then passed through the peroxide xerogel of drying to obtain titanium。But, use H2O2Aqueous solution processes titania cannot generate oxygen-rich silicon dioxide titanium, but in some Ti-O-O-coordinate bonds of titania Surface Creation。This is owing to titanium dioxide is a solid construction, H2O2Molecule can not enter into and to cause inside titania。
At present layered titanic acid is applied to photocatalysis field and has a lot, due to its energy gap relatively big (Eg=3.1~3.5eV), only under ultraviolet light conditions, there is photocatalytic activity。Ultraviolet light only accounts for about 5% in solar spectrum, in order to improve the layered titanic acid utilization rate to sunlight, is presently mainly by layered titanate carrying out solid phase high temperature dopant or carrying out what Heterogeneous Composite realized with other quasiconductor。But the modified speed of these methods is slow, complex process is wayward, is not suitable for producing in enormous quantities。
Summary of the invention
In order to overcome the defect existed in above-mentioned prior art, it is an object of the invention to provide a kind of visible light-responded layered titanic acid photocatalyst and superoxidized modified methods and applications thereof, the method can improve layered titanic acid photocatalysis performance under visible light, reaches the superoxidized modified purpose that layered titanic acid is visible light-responded。
The present invention is achieved through the following technical solutions:
The invention discloses a kind of superoxidized modified method of visible light-responded layered titanic acid photocatalyst, layered titanic acid white powder is joined H2O2In aqueous solution, after stirring reaction, filter, with deionized water wash, dry, obtain visible light-responded layered titanic acid photocatalyst yellow powder body。
Layered metatitanic acid white powder is the titanate with stratiform open architecture, such as H1.07Ti1.73O4、H2Ti4O9、H2Ti3O7、H2Ti5O11、H0.67Ti1.83O4Deng。
Described layered titanic acid white powder and H2O2The amount ratio of aqueous solution is (0.5~1) g:(50~200) mL。
Described H2O2The mass concentration of aqueous solution is 15%~35%。
Described mixing time is 1~10min。
Described baking temperature is 40~80 DEG C。
The invention also discloses and adopt the visible light-responded layered titanic acid photocatalyst prepared with the aforedescribed process, the TiO of this visible light-responded layered titanic acid photocatalyst6Ti-O-O-coordinate bond is there is between octahedral layer。
The energy gap of this visible light-responded layered titanic acid photocatalyst is 2.2~2.5eV。
The invention also discloses the application in degraded environmental contaminants or Organic substance of the above-mentioned visible light-responded layered titanic acid photocatalyst。
Compared with prior art, the present invention has following useful technique effect:
The inventive method selection H2O2Layered titanic acid is carried out superoxidized modified by aqueous solution, owing to layered titanic acid has open architecture, H2O2Molecule is easily advanced into TiO6Between octahedral layer, and and TiO6Titanium in octahedral layer forms Ti-O-O-coordinate bond and then the energy gap of reduction layered titanic acid, has reached layered titanic acid and has had the purpose of photocatalytic activity under visible light。Modified with solid phase high temperature dopant and heterogeneous partly lead compound phase ratio, H2O2It is fast that superoxidized modified layered titanic acid has modified speed, and technical process is simple, it is easy to controls, is suitable in advantages such as production in enormous quantities。
The present invention utilizes the open architecture characteristic of layered titanic acid, dexterously by H2O2Molecule is incorporated into inside (the namely TiO of layered titanic acid6Between between octahedral layer) so that the TiO of the visible light-responded layered titanic acid photocatalyst of preparation6There is substantial amounts of Ti-O-O-coordinate bond between octahedral layer, its energy gap is 2.2~2.5eV, and the visible light catalysis activity than commercialization titanium dioxide P25 is all strong, therefore, there is extensive use in degraded environmental contaminants or Organic substance。
Accompanying drawing explanation
Fig. 1 is a stratiform H prepared by the present invention1.07Ti1.73O4With b peroxidating stratiform H1.07Ti1.73O4Color camera;
Fig. 2 is a stratiform H prepared by the present invention1.07Ti1.73O4With b peroxidating stratiform H1.07Ti1.73O4XRD spectra;
Fig. 3 is stratiform H prepared by the present invention1.07Ti1.73O4With peroxidating stratiform H1.07Ti1.73O4UV-vis DRS spectrogram;
Fig. 4 is stratiform H prepared by the present invention1.07Ti1.73O4With peroxidating stratiform H1.07Ti1.73O4Transient photocurrents figure;
Fig. 5 is stratiform H prepared by the present invention1.07Ti1.73O4With peroxidating stratiform H1.07Ti1.73O4Visible Light Induced Photocatalytic figure to RhB dyestuff。
Detailed description of the invention
Below in conjunction with specific embodiment, the present invention is described in further detail, and the explanation of the invention is not limited。
Embodiment 1
According to layered titanic acid and H2O2The consumption of aqueous solution is 0.5g:200mL, by layered titanic acid H1.07Ti1.73O4White powder joins the H that concentration is 5%2O2In aqueous solution, after stirring 1min, filter, deionized water wash, at 40 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 2
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:50mL, by layered titanic acid white powder H1.07Ti1.73O4Join the H that concentration is 30%2O2In aqueous solution, after stirring 10min, filter, deionized water wash, at 80 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 3
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:50mL, by layered titanic acid white powder H1.07Ti1.73O4Join the H that concentration is 30%2O2In aqueous solution, after stirring 1min, filter, deionized water wash, at 55 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 4
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:50mL, by layered titanic acid white powder H2Ti4O9Join the H that concentration is 10%2O2In aqueous solution, after stirring 5min, filter, deionized water wash, at 55 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 5
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:150mL, by layered titanic acid white powder H2Ti4O9Join the H that concentration is 5%2O2In aqueous solution, after stirring 2min, filter, deionized water wash, at 55 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 6
According to layered titanic acid and H2O2The consumption of aqueous solution is 0.5g:50mL, by layered titanic acid white powder H2Ti4O9Join the H that concentration is 5%2O2In aqueous solution, after stirring 1min, filter, deionized water wash, at 40 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 7
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:200mL, by layered titanic acid white powder H2Ti5O11, join the H that concentration is 30%2O2In aqueous solution, after stirring 10min, filter, deionized water wash, at 80 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 8
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:100mL, by layered titanic acid white powder H2Ti5O11, join the H that concentration is 10%2O2In aqueous solution, after stirring 5min, filter, deionized water wash, at 60 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 9
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:50mL, by layered titanic acid white powder H2Ti5O11, join the H that concentration is 30%2O2In aqueous solution, after stirring 2min, filter, deionized water wash, at 80 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 10
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:200mL, by layered titanic acid white powder H0.67Ti1.83O4Join the H that concentration is 30%2O2In aqueous solution, after stirring 10min, filter, deionized water wash, at 80 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 11
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:100mL, by layered titanic acid white powder H0.67Ti1.83O4Join the H that concentration is 10%2O2In aqueous solution, after stirring 5min, filter, deionized water wash, at 60 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Embodiment 12
According to layered titanic acid and H2O2The consumption of aqueous solution is 1g:50mL, by layered titanic acid white powder H0.67Ti1.83O4Join the H that concentration is 30%2O2In aqueous solution, after stirring 2min, filter, deionized water wash, at 80 DEG C, obtain yellow peroxidating layered titanic acid powder body after dry 1h。
Referring to Fig. 1, from fig. 1, it can be seen that powder body is white in a, peroxidating stratiform H in b1.07Ti1.73O4Present yellow。Referring to Fig. 2, as can be seen from Figure 2, the all of diffraction maximum of layered titanic acid is all substantially identical with peroxidating layered titanic acid, layer structure after hydrogen peroxide process and untreated front not change are described, simply in the diffraction maximum of (020) crystal face from 9.68 ° of left shift to 9.12 °, corresponding TiO6Octahedral layer spacing has expanded 9.697nm to from 9.137nm, illustrates that hydrogen peroxide enters interlayer so that interlamellar spacing increases。Fig. 3 is stratiform H prepared by the present invention1.07Ti1.73O4With peroxidating stratiform H1.07Ti1.73O4UV-vis DRS spectrogram, as can be seen from Figure 3, it was shown that the absorption band edge of peroxidating layered titanic acid light is 550nm, namely energy gap is 2.2eV。
Fig. 4 is stratiform H prepared by the present invention1.07Ti1.73O4With peroxidating stratiform H1.07Ti1.73O4Transient photocurrents figure;As can be seen from Figure 4, peroxidating layered titanic acid can effectively suppress efficiently separating of photo-generate electron-hole。Fig. 5 is stratiform H prepared by the present invention1.07Ti1.73O4With peroxidating stratiform H1.07Ti1.73O4Visible Light Induced Photocatalytic figure to RhB dyestuff;As can be seen from Figure 5, the relative layered titanic acid of peroxidating layered titanic acid is greatly improved, and the visible light catalysis activity than commercialization titanium dioxide P25 is all strong。
Above said content is in conjunction with concrete preferred implementation further description made for the present invention, it is not all of or unique embodiment, the conversion of any equivalence that technical solution of the present invention is taked by those of ordinary skill in the art by reading description of the present invention, the claim being the present invention is contained。

Claims (9)

1. the superoxidized modified method of layered titanic acid photocatalyst one kind visible light-responded, it is characterised in that layered titanic acid white powder is joined H2O2In aqueous solution, after stirring reaction, filter, with deionized water wash, dry, obtain visible light-responded layered titanic acid photocatalyst yellow powder body。
2. the superoxidized modified method of visible light-responded layered titanic acid photocatalyst according to claim 1, it is characterised in that layered metatitanic acid white powder is the titanate with stratiform open architecture。
3. the superoxidized modified method of visible light-responded layered titanic acid photocatalyst according to claim 1, it is characterised in that described layered titanic acid white powder and H2O2The amount ratio of aqueous solution is (0.5~1) g:(50~200) mL。
4. the superoxidized modified method of visible light-responded layered titanic acid photocatalyst according to claim 1, it is characterised in that described H2O2The mass concentration of aqueous solution is 15%~35%。
5. the superoxidized modified method of visible light-responded layered titanic acid photocatalyst according to claim 1, it is characterised in that described mixing time is 1~10min。
6. the superoxidized modified method of visible light-responded layered titanic acid photocatalyst according to claim 1, it is characterised in that described baking temperature is 40~80 DEG C。
7. adopt in claim 1~6 the visible light-responded layered titanic acid photocatalyst that the method described in any one prepares, it is characterised in that the TiO of this visible light-responded layered titanic acid photocatalyst6Ti-O-O-coordinate bond is there is between octahedral layer。
8. visible light-responded layered titanic acid photocatalyst according to claim 7, it is characterised in that the energy gap of this visible light-responded layered titanic acid photocatalyst is 2.2~2.5eV。
9. the application in degraded environmental contaminants or Organic substance of the visible light-responded layered titanic acid photocatalyst described in claim 7 or 8。
CN201610178898.0A 2016-03-25 2016-03-25 Visible light responded layered titanic acid photocatalyst as well as peroxidation modifying method and application of visible light responded layered titanic acid photocatalyst Pending CN105689015A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610178898.0A CN105689015A (en) 2016-03-25 2016-03-25 Visible light responded layered titanic acid photocatalyst as well as peroxidation modifying method and application of visible light responded layered titanic acid photocatalyst

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610178898.0A CN105689015A (en) 2016-03-25 2016-03-25 Visible light responded layered titanic acid photocatalyst as well as peroxidation modifying method and application of visible light responded layered titanic acid photocatalyst

Publications (1)

Publication Number Publication Date
CN105689015A true CN105689015A (en) 2016-06-22

Family

ID=56232879

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610178898.0A Pending CN105689015A (en) 2016-03-25 2016-03-25 Visible light responded layered titanic acid photocatalyst as well as peroxidation modifying method and application of visible light responded layered titanic acid photocatalyst

Country Status (1)

Country Link
CN (1) CN105689015A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106861669A (en) * 2017-02-27 2017-06-20 陕西科技大学 A kind of porous laminated structure metatitanic acid particle and preparation method thereof
CN106925260A (en) * 2017-02-27 2017-07-07 陕西科技大学 A kind of Ag2Titanium oxide of O cluster intercalations and its preparation method and application
CN106944035A (en) * 2017-02-27 2017-07-14 陕西科技大学 A kind of oxygen auto-dope stratiform niobium oxide powder and its preparation method and application
CN108511730A (en) * 2018-05-03 2018-09-07 陕西科技大学 A kind of holey Zn2Ti3O8/TiO2Nano combined platy particle and its preparation method and application
CN109092055A (en) * 2018-10-16 2018-12-28 上海朗绿建筑科技股份有限公司 A kind of formaldehyde adsorbent and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101757937A (en) * 2009-11-24 2010-06-30 江苏工业学院 Titanium dioxide intercalation photocatalysed composite material and preparation method thereof
CN102266748A (en) * 2011-06-09 2011-12-07 中山大学 Method for preparing titanic acid/titanium dioxide mixed nano-powder material
CN103170320A (en) * 2013-04-02 2013-06-26 常州大学 Preparation method of stratified columnar titanium dioxide photocatalyst
CN103950944A (en) * 2014-04-25 2014-07-30 浙江大学 Sheet mineral and nano titanium dioxide intercalating composite material and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101757937A (en) * 2009-11-24 2010-06-30 江苏工业学院 Titanium dioxide intercalation photocatalysed composite material and preparation method thereof
CN102266748A (en) * 2011-06-09 2011-12-07 中山大学 Method for preparing titanic acid/titanium dioxide mixed nano-powder material
CN103170320A (en) * 2013-04-02 2013-06-26 常州大学 Preparation method of stratified columnar titanium dioxide photocatalyst
CN103950944A (en) * 2014-04-25 2014-07-30 浙江大学 Sheet mineral and nano titanium dioxide intercalating composite material and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
YAN WANG ET AL.: ""Recoverable visible light photocatalytic activity of wide band gap nanotubular titanic acid induced by H2O2-pretreatment"", 《APPLIED CATALYSIS B: ENVIRONMENTAL》 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106861669A (en) * 2017-02-27 2017-06-20 陕西科技大学 A kind of porous laminated structure metatitanic acid particle and preparation method thereof
CN106925260A (en) * 2017-02-27 2017-07-07 陕西科技大学 A kind of Ag2Titanium oxide of O cluster intercalations and its preparation method and application
CN106944035A (en) * 2017-02-27 2017-07-14 陕西科技大学 A kind of oxygen auto-dope stratiform niobium oxide powder and its preparation method and application
CN106861669B (en) * 2017-02-27 2019-06-04 陕西科技大学 A kind of porous laminated structure metatitanic acid particle and preparation method thereof
CN106944035B (en) * 2017-02-27 2019-08-06 陕西科技大学 A kind of oxygen auto-dope stratiform niobium oxide powder and its preparation method and application
CN106925260B (en) * 2017-02-27 2020-05-19 陕西科技大学 Ag2O-cluster intercalated titanium oxide and preparation method and application thereof
CN108511730A (en) * 2018-05-03 2018-09-07 陕西科技大学 A kind of holey Zn2Ti3O8/TiO2Nano combined platy particle and its preparation method and application
CN109092055A (en) * 2018-10-16 2018-12-28 上海朗绿建筑科技股份有限公司 A kind of formaldehyde adsorbent and preparation method thereof

Similar Documents

Publication Publication Date Title
Zhu et al. Hierarchical ZnO decorated with CeO2 nanoparticles as the direct Z-scheme heterojunction for enhanced photocatalytic activity
CN105689015A (en) Visible light responded layered titanic acid photocatalyst as well as peroxidation modifying method and application of visible light responded layered titanic acid photocatalyst
Wang et al. Synthesis of gC 3 N 4/NiO p–n heterojunction materials with ball-flower morphology and enhanced photocatalytic performance for the removal of tetracycline and Cr 6+
US9868114B2 (en) Preparation method of fluorine-doped lamellar black titanium dioxide nano material
CN102974373B (en) Preparation method of visible-light photocatalytic material
CN103285861B (en) An Ag3VO4/TiO2 compound nano-wire having visible light activity, a preparation method and applications thereof
CN108993604B (en) High visible light activity AgIn5S8/UIO-66-NH2Composite material and preparation method and application thereof
CN106669744B (en) Ag2Mo2O7@ AgBr composite photocatalyst and preparation method thereof
CN106000431B (en) Sheet CdS/BiOCl composite nano materials and preparation method thereof
CN105170173B (en) A kind of perovskite material/organic polymer composite photo-catalyst, preparation and application
Cao et al. A novel Bi12TiO20/g-C3N4 hybrid catalyst with a bionic granum configuration for enhanced photocatalytic degradation of organic pollutants
Abdellatif et al. A highly efficient dual-phase GaN (O)/Nb2O5 (N) photocatalyst prepared through nitridation and reoxidation process for NO removal
CN103877966A (en) Preparation method of heterostructure photocatalyst
Selvaratnam et al. TiO2-MgO mixed oxide nanomaterials for solar energy conversion
CN103613130B (en) Preparation method of titanium dioxide nanowire-lead sulfide quantum dot composite material
CN105879857A (en) Titanium dioxide rod catalyst doped with bismuth molybdate nanosheets
Garay-Rodríguez et al. Photocatalytic evaluation of composites of Ba3Li2Ti8O20-CuO in the reduction of CO2 to formaldehyde under visible light irradiation
CN105905940A (en) Preparation method of nickel titanate/titanium dioxide composite nanomaterial
CN104226320B (en) The preparation method of vanadium boron codope titanium dioxide and nickel oxide composite photo-catalyst
Wu et al. Solvothermal synthesis of Bi2O3/BiVO4 heterojunction with enhanced visible-light photocatalytic performances
Tavakoli-Azar et al. Enhanced photocatalytic activity of ZrO2-CdZrO3-S nanocomposites for degradation of Crystal Violet dye under sunlight
CN104998666B (en) A kind of method and catalyst applications for preparing bowknot shape fluorine oxygen bismuth photochemical catalyst
CN107362792A (en) A kind of preparation method of strontium titanates/niobic acid tin composite nano materials
CN105080573B (en) One kind prepares SnS using microwave-hydrothermal method2/SnO2The method of nano-photo catalytic composite
CN106944035B (en) A kind of oxygen auto-dope stratiform niobium oxide powder and its preparation method and application

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

Application publication date: 20160622

RJ01 Rejection of invention patent application after publication