CN116550320A - Synthesis method of manganese dioxide nano material with neuron-like cell structure - Google Patents

Synthesis method of manganese dioxide nano material with neuron-like cell structure Download PDF

Info

Publication number
CN116550320A
CN116550320A CN202310536414.5A CN202310536414A CN116550320A CN 116550320 A CN116550320 A CN 116550320A CN 202310536414 A CN202310536414 A CN 202310536414A CN 116550320 A CN116550320 A CN 116550320A
Authority
CN
China
Prior art keywords
manganese dioxide
manganese
cell structure
neuron
nanomaterial
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.)
Granted
Application number
CN202310536414.5A
Other languages
Chinese (zh)
Other versions
CN116550320B (en
Inventor
郝新丽
郑钰涛
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.)
Hebei GEO University
Original Assignee
Hebei GEO University
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 Hebei GEO University filed Critical Hebei GEO University
Priority to CN202310536414.5A priority Critical patent/CN116550320B/en
Publication of CN116550320A publication Critical patent/CN116550320A/en
Application granted granted Critical
Publication of CN116550320B publication Critical patent/CN116550320B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C02F1/72Treatment of water, waste water, or sewage by oxidation
    • C02F1/725Treatment of water, waste water, or sewage by oxidation by catalytic oxidation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/32Manganese, technetium or rhenium
    • B01J23/34Manganese
    • 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
    • B01J35/40Catalysts, in general, characterised by their form or physical properties characterised by dimensions, e.g. grain size
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G45/00Compounds of manganese
    • C01G45/02Oxides; Hydroxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/70Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • C01P2002/72Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/01Particle morphology depicted by an image
    • C01P2004/03Particle morphology depicted by an image obtained by SEM
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/64Nanometer sized, i.e. from 1-100 nanometer
    • 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/30Wastewater or sewage treatment systems using renewable energies
    • Y02W10/37Wastewater or sewage treatment systems using renewable energies using solar energy

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Environmental & Geological Engineering (AREA)
  • Water Supply & Treatment (AREA)
  • Inorganic Chemistry (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

The invention relates to the technical field of manganese dioxide nano materials, and provides a synthesis method of a manganese dioxide nano material with a neuron-like cell structure, which comprises the following steps: KMnO 4 Mixing the solution with a divalent manganese salt solution to obtain a mixture, and reacting to obtain a manganese dioxide nano material; KMnO in the mixture 4 And a molar ratio of divalent manganese salt of 1:2; the reaction temperature is 90 ℃ and the reaction time is 1.5h. Through the technical scheme, the problem of poor degradation effect of the manganese dioxide nano material in the prior art is solved.

Description

Synthesis method of manganese dioxide nano material with neuron-like cell structure
Technical Field
The invention relates to the technical field of manganese dioxide nano materials, in particular to a synthesis method of a manganese dioxide nano material with a neuron-like cell structure.
Background
Manganese dioxide has great application potential in catalyzing and degrading organic dye, and can decompose hydrogen peroxide to produce hydroxyl radical with strong oxidizing property, and the hydroxyl radical can effectively oxidize and degrade the organic dye. Some researches at home and abroad adopt manganese dioxide to catalyze and degrade organic dye, and common preparation methods of the manganese dioxide mainly comprise the following steps: anodic electrodeposition, coprecipitation, sol-gel, ultrasonic assisted redox, electrokinetic deposition, decomposition, hydrothermal, etc. The manganese dioxide material prepared at present has a flower-like structure, a one-dimensional structure, a particle structure and the like, and manganese dioxide with different structures and morphologies has different degradation effects. At present, the synthesized manganese dioxide nano material has the problem of poor degradation effect.
Disclosure of Invention
The invention provides a synthesis method of manganese dioxide nano-materials with neuron-like cell structures, which solves the problem of poor degradation effect of manganese dioxide nano-materials in the related technology.
The technical scheme of the invention is as follows:
the synthesis method of the manganese dioxide nano material with the neuron-like cell body structure comprises the following steps: KMnO 4 Mixing the solution with a divalent manganese salt solution to obtain a mixture, and reacting to obtain the manganese dioxide nano material with the neuron-like cell structure; KMnO in the mixture 4 And a molar ratio of divalent manganese salt of 1:2; the reaction temperature is 90 ℃ and the reaction time is 1.5h.
As a further technical scheme, the KMnO 4 The concentration of the solution is 0.020-0.030mol/L.
As a further technical scheme, the KMnO 4 The concentration of the solution was 0.025mol/L.
As a further technical scheme, the concentration of manganese ions in the divalent manganese salt solution is 0.05-0.15mol/L
As a further technical scheme, the concentration of manganese ions in the divalent manganese salt solution is 0.1mol/L.
As a further technical scheme, the divalent manganese salt comprises one of manganese acetate, manganese sulfate and manganese nitrate.
As a further technical scheme, the divalent manganese salt is manganese acetate.
According to the technical scheme, after the reaction, the obtained precipitate is filtered, washed by distilled water, dried and ground to obtain the manganese dioxide nano material with the neuron-like cell structure.
The invention also comprises the manganese dioxide nanomaterial with the neuron-like cell structure obtained by the synthesis method of the manganese dioxide nanomaterial with the neuron-like cell structure.
As a further technical scheme, the manganese dioxide nanomaterial with the neuron-like cell structure is applied to degradation of organic dye.
As a further technical scheme, the organic dye is rhodamine B.
The working principle and the beneficial effects of the invention are as follows:
1. according to the invention, the manganese dioxide nanomaterial of neuron cell bodies is obtained after reaction by controlling the molar ratio of potassium permanganate to divalent manganese salt to be 1:2, and the manganese dioxide nanomaterial has high degradation performance, is reacted for 60min, has a degradation rate of rhodamine B as high as 99.30%, is fast in degradation reaction, and has a degradation rate higher than that of the manganese dioxide nanomaterial with a flower-like and one-dimensional structure measured at 5min, 20min, 40min and 60 min.
2. In the invention, when the reaction temperature is 90 ℃ and the reaction time is 1.5h, under the reaction condition, KMnO is controlled 4 The molar ratio of the manganese dioxide salt to the divalent manganese salt is 1:2, so that the prepared manganese dioxide nano material has higher degradability.
Drawings
The invention will be described in further detail with reference to the drawings and the detailed description.
FIG. 1 is a Scanning Electron Microscope (SEM) topography (5 ten thousand times) of a manganese dioxide nanomaterial of example 1 of the present invention;
FIG. 2 is a Scanning Electron Microscope (SEM) topography (1 ten thousand times) of a manganese dioxide nanomaterial of example 1 of the present invention;
FIG. 3 is a Scanning Electron Microscope (SEM) topography (5 ten thousand times) of the manganese dioxide nanomaterial of comparative example 1 of the present invention;
FIG. 4 is a Scanning Electron Microscope (SEM) topography (3 ten thousand times) of the manganese dioxide nanomaterial of comparative example 2 of the present invention;
FIG. 5 is a Scanning Electron Microscope (SEM) topography (1 ten thousand times) of the manganese dioxide nanomaterial of comparative example 3 of the present invention;
FIG. 6 is a Scanning Electron Microscope (SEM) topography (3 ten thousand times) of a manganese dioxide nanomaterial of comparative example 4 of the present invention;
FIG. 7 is an X-ray diffraction (XRD) spectrum of a manganese dioxide nanomaterial of example 1 of the present invention;
FIG. 8 is an X-ray diffraction (XRD) spectrum of a manganese dioxide nanomaterial of comparative example 1 of the present invention;
FIG. 9 is an X-ray diffraction (XRD) spectrum of a manganese dioxide nanomaterial of comparative example 3 of the present invention;
FIG. 10 is an X-ray diffraction (XRD) spectrum of a manganese dioxide nanomaterial of comparative example 4 of the present invention;
FIG. 11 is a graph showing the ultraviolet-visible spectrum of the degradation process of manganese dioxide nanomaterial of example 1 of the present invention;
FIG. 12 is a graph of the ultraviolet-visible spectrum of the degradation process of the manganese dioxide nanomaterial of comparative example 1 of the present invention;
FIG. 13 is a graph of the ultraviolet visible spectrum of the degradation process of the manganese dioxide nanomaterial of comparative example 3 of the present invention.
Detailed Description
The technical solutions of the embodiments of the present invention will be clearly and completely described below in conjunction with the embodiments of the present invention, and it is apparent that the described embodiments are only some embodiments of the present invention, not all embodiments. All other embodiments, which can be made by one of ordinary skill in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
Example 1
KMnO 4 The solution (0.025 mol/L,200 mL) was poured into Mn (CH) 3 COO) 2 In the solution (0.1 mol/L,100 mL), after reacting for 1.5h in a constant temperature water bath kettle at 90 ℃, carrying out suction filtration on the obtained precipitate, washing with distilled water, drying in an oven, grinding into powder to obtain manganese dioxide nano material, wherein a Scanning Electron Microscope (SEM) topography chart is shown in FIG. 1 and FIG. 2, an XRD spectrum chart is shown in FIG. 7, and the obtained product is shown as MnO 2
Comparative example 1
KMnO 4 The solution (0.05 mol/L,200 mL) was poured into Mn (CH) 3 COO) 2 In solution (0.1 mol/L,100 mL)After reacting for 1.5h in a constant temperature water bath kettle at 90 ℃ under stirring, filtering the obtained precipitate, washing with distilled water, drying in an oven, grinding into powder to obtain manganese dioxide nanomaterial, wherein a Scanning Electron Microscope (SEM) topography is shown in FIG. 3, an XRD spectrum is shown in FIG. 8, and the obtained product is K 0.46 Mn 2 O 4 ·1.4H 2 O (birnessite type MnO) 2 )。
Comparative example 2
KMnO 4 The solution (0.034 mol/L,200 mL) was poured into Mn (CH) 3 COO) 2 In the solution (0.1 mol/L,100 mL), the obtained precipitate is subjected to suction filtration after being reacted for 1.5h in a constant temperature water bath kettle at 90 ℃ under the stirring condition, and is washed by distilled water, is put into an oven for drying and is ground into powder, so that the manganese dioxide nano material is obtained, and a Scanning Electron Microscope (SEM) morphology graph is shown in figure 4.
Comparative example 3
KMnO 4 The solution (0.00625 mol/L,200 mL) was poured into Mn (CH) 3 COO) 2 In the solution (0.1 mol/L,100 mL), after reacting for 1.5h under the condition of stirring in a constant-temperature water bath at 90 ℃, carrying out suction filtration on the obtained precipitate, washing with distilled water, drying in an oven, grinding into powder to obtain manganese dioxide nano material, wherein a Scanning Electron Microscope (SEM) topography is shown as figure 5, an XRD spectrum is shown as figure 9, and the obtained product is MnO x A complex.
Comparative example 4
KMnO 4 The solution (0.025 mol/L,200 mL) was poured into Mn (CH) 3 COO) 2 In the solution (0.1 mol/L,100 mL), after reacting for 2 hours in a constant temperature water bath kettle at 90 ℃, carrying out suction filtration on the obtained precipitate, washing with distilled water, putting into a baking oven for drying, and grinding into powder to obtain manganese dioxide nano material, wherein a Scanning Electron Microscope (SEM) morphology chart is shown in figure 6, an XRD spectrum is shown in figure 10, and the obtained product is shown as K 0.46 Mn 2 O 4 ·1.4H 2 O (birnessite type MnO) 2 )。
Comparative examples 1-3 modified KMnO compared to example 1 4 And Mn (CH) 3 COO) 2 From FIGS. 1 to 2, the molar ratio of (C)In the present invention, the manganese dioxide nanomaterial prepared in example 1 is of a neuronal cell-like structure, and as can be seen from fig. 3 to 4, the manganese dioxide nanomaterial prepared in comparative examples 1 to 2 is of a flower-like structure, and as can be seen from fig. 5, the manganese dioxide nanomaterial prepared in comparative example 3 is of a one-dimensional structure.
As a result of changing the time during the preparation process as compared with example 1 in comparative example 4, it can be seen from fig. 6 that the manganese dioxide nanomaterial prepared in comparative example 4 has a particle structure, indicating that the manganese dioxide nanomaterial having a neuronal cell-like structure cannot be synthesized by changing the preparation time.
Test example-catalytic test
Under the condition of pH 3, 100mL of rhodamine B (RhB) solution with concentration of 10mg/L is degraded by using 10mg of manganese dioxide nanomaterial, the catalytic performance of the manganese dioxide nanomaterial of example 1 and the manganese dioxide nanomaterial of comparative examples 1 and 3 are respectively measured, ultraviolet visible spectrum diagrams of degradation processes are shown in figures 11-13, and degradation rates of different reaction times are shown in table 1.
TABLE 1 degradation rates of manganese dioxide nanomaterials of example 1 and comparative examples 1 and 3 at different times
5min(%) 20min(%) 40min(%) 60min(%)
Example 1 93.34 98.83 99.44 99.43
Comparative example 1 90.49 98.59 99.27 99.32
Comparative example 3 79.91 92.40 97.64 99.10
As can be seen from Table 1, the degradation rates of the manganese dioxide nanomaterial of example 1 in 5min, 20min, 40min and 60min are all larger than those of comparative example 1 and comparative example 3, and the degradation rate of the manganese dioxide nanomaterial of example 1 in 60min is as high as 99.43%, which indicates that the manganese dioxide nanomaterial of neuron-like cell structure prepared by the invention has high degradation rate, quick degradation reaction and good catalytic performance. The performance of the manganese dioxide nanomaterial with the particle structure is similar to that of the manganese dioxide nanomaterial with the flower-shaped structure, so that the manganese dioxide nanomaterial with the particle structure obtained in comparative example 4 is not subjected to a catalytic test.
The foregoing description of the preferred embodiments of the invention is not intended to be limiting, but rather is intended to cover all modifications, equivalents, alternatives, and improvements that fall within the spirit and scope of the invention.

Claims (9)

1. The synthesis method of the manganese dioxide nano material with the neuron-like cell body structure is characterized by comprising the following steps of: KMnO 4 Mixing the solution with a divalent manganese salt solution to obtain a mixture, and reacting to obtain the manganese dioxide nano material with the neuron-like cell structure; the said mixingKMnO in the compound 4 And a molar ratio of divalent manganese salt of 1:2; the reaction temperature is 90 ℃ and the reaction time is 1.5h.
2. The method of claim 1, wherein KMnO 4 The concentration of the solution is 0.020-0.030mol/L.
3. The method for synthesizing manganese dioxide nanomaterial of neuronal cell structure according to claim 1, wherein the concentration of manganese ions in the divalent manganese salt solution is 0.05-0.15mol/L.
4. The method of synthesizing a neuronal cell structure manganese dioxide nanomaterial according to claim 1, wherein the divalent manganese salt comprises one of manganese acetate, manganese sulfate and manganese nitrate.
5. The method of claim 4, wherein the manganese dioxide nano-material is manganese acetate.
6. The method for synthesizing the manganese dioxide nanomaterial with the neuron-like cell structure according to claim 1, wherein after the reaction, the obtained precipitate is filtered, washed by distilled water, dried and ground to obtain the manganese dioxide nanomaterial with the neuron-like cell structure.
7. A manganese dioxide nanomaterial of neuronal cell structure obtainable by the method of synthesis of a manganese dioxide nanomaterial of neuronal cell structure as claimed in any of claims 1 to 6.
8. The use of manganese dioxide nanomaterial of neuronal cell like structure according to claim 7 for degrading organic dyes.
9. The use of manganese dioxide nanomaterial of neuronal cell structure according to claim 8 for degrading organic dye, wherein the organic dye is rhodamine B.
CN202310536414.5A 2023-05-12 2023-05-12 Synthesis method of manganese dioxide nano material with neuron-like cell structure Active CN116550320B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202310536414.5A CN116550320B (en) 2023-05-12 2023-05-12 Synthesis method of manganese dioxide nano material with neuron-like cell structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202310536414.5A CN116550320B (en) 2023-05-12 2023-05-12 Synthesis method of manganese dioxide nano material with neuron-like cell structure

Publications (2)

Publication Number Publication Date
CN116550320A true CN116550320A (en) 2023-08-08
CN116550320B CN116550320B (en) 2024-02-02

Family

ID=87499714

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202310536414.5A Active CN116550320B (en) 2023-05-12 2023-05-12 Synthesis method of manganese dioxide nano material with neuron-like cell structure

Country Status (1)

Country Link
CN (1) CN116550320B (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6230622A (en) * 1985-08-02 1987-02-09 Chuo Denki Kogyo Kk Production of manganese dioxide
CN101798118A (en) * 2010-03-11 2010-08-11 湘潭大学 Preparation method of manganese dioxide one-dimensional nanomaterial
CN102910680A (en) * 2012-10-22 2013-02-06 天津大学 Preparation method for preparing manganese dioxides in various crystal forms
US20130064972A1 (en) * 2010-03-26 2013-03-14 Hideki Koyanaka Methods for synthesizing nanometer-sized manganese dioxides having ramsdellite-type crystal structures as well as methods for producing hydroxide ion-derived proton, electron and oxygen using manganese dioxides
CN109437309A (en) * 2018-11-26 2019-03-08 郝新丽 A kind of synthetic method of shuttle-type structure manganese carbonate nano material
CN113181943A (en) * 2021-03-15 2021-07-30 广东工业大学 MnO (MnO)2Composite g-C3N4Material, preparation method and application thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6230622A (en) * 1985-08-02 1987-02-09 Chuo Denki Kogyo Kk Production of manganese dioxide
CN101798118A (en) * 2010-03-11 2010-08-11 湘潭大学 Preparation method of manganese dioxide one-dimensional nanomaterial
US20130064972A1 (en) * 2010-03-26 2013-03-14 Hideki Koyanaka Methods for synthesizing nanometer-sized manganese dioxides having ramsdellite-type crystal structures as well as methods for producing hydroxide ion-derived proton, electron and oxygen using manganese dioxides
CN102910680A (en) * 2012-10-22 2013-02-06 天津大学 Preparation method for preparing manganese dioxides in various crystal forms
CN109437309A (en) * 2018-11-26 2019-03-08 郝新丽 A kind of synthetic method of shuttle-type structure manganese carbonate nano material
CN113181943A (en) * 2021-03-15 2021-07-30 广东工业大学 MnO (MnO)2Composite g-C3N4Material, preparation method and application thereof

Also Published As

Publication number Publication date
CN116550320B (en) 2024-02-02

Similar Documents

Publication Publication Date Title
US10486138B2 (en) Method for hydrothermal synthesis of three dimensional Bi4MoO9/TiO2 nanostructure heterojunction
CN110918126B (en) Preparation method of flower-shaped molybdenum disulfide combined UiO-66 photocatalyst
Zhou et al. Fabrication of walnut-like BiVO4@ Bi2S3 heterojunction for efficient visible photocatalytic reduction of Cr (VI)
CN106493386A (en) The octahedral shape Nanoalloy of octahedra Nanoalloy and porous, Preparation Method And The Use
Wang et al. Optimized design of BiVO4/NH2-MIL-53 (Fe) heterostructure for enhanced photocatalytic degradation of methylene blue and ciprofloxacin under visible light
KR101830575B1 (en) Ag-ZnFe2O4@rGO Nanocomposite Photocatalyst for Efficient Treatment of Organic Wastes under Ultraviolet and Visible Light and the Preparation Method Thereof
CN113402726B (en) Prussian blue analogue nano-framework material and preparation method and application thereof
US20230372918A1 (en) Photocatalytic material for efficient photocatalytic removal of high-concentration nitrate, and preparation method and use thereof
EP2921456A2 (en) Material used in the removal of contaminants from liquid matrices
CN109621961B (en) Method for in-situ preparation of metal high-dispersion catalyst by growing two-dimensional nanosheets
CN114272944B (en) Silver phosphate/cobalt tungstate composite sound catalytic material and preparation method and application thereof
CN105772039A (en) Fluorine and boron co-doped TiO2 nano-plate with crystal planes (001) and oxygen vacancy, method for preparing fluorine and boron co-doped TiO2 nano-plate and application thereof
CN113830826A (en) Method for preparing shell-core structure mesoporous quantum titanium oxide by precipitation-self-assembly method
CN115069265A (en) Preparation and application of active carbon fiber loaded cobalt-manganese bimetallic oxide catalyst
CN114308073B (en) Preparation method and application of composite catalyst
CN113818043A (en) Bismuth vanadate-metal organic complex composite photoelectrode and preparation method and application thereof
CN108404926B (en) Amorphous ferric vanadate/bismuth vanadate/graphene composite photocatalyst and preparation method and application thereof
CN116550320B (en) Synthesis method of manganese dioxide nano material with neuron-like cell structure
CN114084907A (en) Mesoporous manganese dioxide synthesized by redox method, metal-doped mesoporous manganese dioxide and method
CN113600174A (en) Bismuth-bismuth oxycarbonate composite photocatalyst and preparation method and application thereof
CN113415821A (en) Hollow ZnxCd1-xPreparation method and application of S solid solution nanosphere
CN111545245A (en) Iron ion doped metal organic framework material and preparation method thereof
CN116676633A (en) Shape-adjustable Pt-TiO 2 Preparation method and application of catalyst
CN114917932B (en) For CO 2 Photo-reduction synthesis of CO and H 2 Catalyst, preparation method and application thereof
CN116943692A (en) Bismuth ferrite/bismuth oxysulfate/ferric oxide strip composite material and preparation method and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant