CN110203925B - Recovery method of overdue donkey-hide gelatin waste drug - Google Patents

Recovery method of overdue donkey-hide gelatin waste drug Download PDF

Info

Publication number
CN110203925B
CN110203925B CN201910439561.4A CN201910439561A CN110203925B CN 110203925 B CN110203925 B CN 110203925B CN 201910439561 A CN201910439561 A CN 201910439561A CN 110203925 B CN110203925 B CN 110203925B
Authority
CN
China
Prior art keywords
donkey
hide gelatin
overdue
waste
drugs
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
CN201910439561.4A
Other languages
Chinese (zh)
Other versions
CN110203925A (en
Inventor
侯宏英
刘显茜
余成义
李栋栋
代志鹏
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.)
Kunming University of Science and Technology
Original Assignee
Kunming 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 Kunming University of Science and Technology filed Critical Kunming University of Science and Technology
Priority to CN201910439561.4A priority Critical patent/CN110203925B/en
Publication of CN110203925A publication Critical patent/CN110203925A/en
Application granted granted Critical
Publication of CN110203925B publication Critical patent/CN110203925B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/30Active carbon
    • C01B32/312Preparation
    • C01B32/318Preparation characterised by the starting materials
    • C01B32/324Preparation characterised by the starting materials from waste materials, e.g. tyres or spent sulfite pulp liquor
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/054Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/362Composites
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H01M4/587Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
    • 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
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Environmental & Geological Engineering (AREA)
  • Composite Materials (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Secondary Cells (AREA)

Abstract

The invention discloses a method for recovering overdue donkey-hide gelatin waste drugs, which is characterized in that nitrogen/sulfur co-doped solid carbon microspheres are obtained by recovering the overdue donkey-hide gelatin waste drugs through hydrothermal reaction and pyrolysis carbonization; or adding ferroferric oxide nanospheres as templates to obtain nitrogen/sulfur co-doped hollow carbon nanospheres under the same condition; assembling the product and a sodium foil into a simulated sodium-ion battery, and testing the electrochemical sodium storage performance of the battery; the invention provides a new way and a new scheme for recycling overdue donkey-hide gelatin waste drugs based on the environmental protection concept of changing waste into valuable and recycling economy and aiming at exploring secondary non-medical value in the overdue drugs, and has the advantages of environmental friendliness, low cost and strong practicability, and has important social and environmental protection significance for developing green energy and recycling economy of the overdue donkey-hide gelatin waste drugs.

Description

Recovery method of overdue donkey-hide gelatin waste drug
Technical Field
The invention relates to a method for recovering expired donkey-hide gelatin waste drug, aims to develop and utilize secondary non-medical value in the expired donkey-hide gelatin waste drug, and belongs to the field of research of new energy materials.
Background
As a famous traditional Chinese medicine, donkey-hide gelatin is prepared by taking donkey skin as a raw material through decoction and concentration, mainly contains 18 amino acids and collagen hydrolysate with small molecular weight, and is widely used for treating diseases such as anemia, deficiency of both qi and blood, palpitation and insomnia, inappetence and the like. Unfortunately, the wide use and the over-demand of the donkey-hide gelatin drug inevitably lead to the fact that the donkey-hide gelatin drug cannot be used in the effective period in time and is wasted in the healing period. In particular, bottled liquid drugs are more likely to break down and contaminate groundwater systems or stab sanitation workers than other packaging formats. Incineration or centralized landfill are two main treatment modes for treating overdue waste drugs at present, but the two main treatment modes are contrary to the concepts of circular economy and sustainable development, so that a more friendly and reasonable management scheme needs to be found, and secondary non-medical values in the overdue drugs are fully utilized.
Considering that the overdue donkey-hide gelatin waste medicine contains abundant carbon elements and a small amount of nitrogen elements and sulfur elements, the overdue donkey-hide gelatin waste medicine may be a satisfactory nitrogen/sulfur co-doped carbon source precursor, but no relevant research report exists at present.
Disclosure of Invention
The invention provides a method for recycling overdue donkey-hide gelatin waste, which comprises the steps of adding water into the overdue donkey-hide gelatin waste to prepare a donkey-hide gelatin solution, carrying out hydrothermal reaction on the donkey-hide gelatin solution at the temperature of 180-200 ℃ for 3-6 h, then carrying out pyrolysis carbonization at the temperature of 600-900 ℃ for 1-3 h in a tubular furnace under an inert atmosphere, carrying out furnace cooling, and carrying out acid pickling, water washing and drying to obtain black powder.
A method for recycling overdue donkey-hide gelatin waste medicines comprises the steps of adding water to the overdue donkey-hide gelatin waste medicines to prepare a donkey-hide gelatin solution, adding template agent ferroferric oxide nanospheres, mixing uniformly, carrying out hydrothermal reaction on the mixture at 180-200 ℃ for 3-6 hours, then carrying out pyrolysis carbonization in a tubular furnace at 600-900 ℃ for 1-3 hours under inert atmosphere, carrying out furnace cooling, carrying out acid washing, water washing and drying to obtain black powder.
The concentration of the donkey-hide gelatin solution is 0.05-0.2 g/mL.
The mass ratio of the overdue donkey-hide gelatin waste drug to the ferroferric oxide nanospheres is 20-30: 1.
The obtained black powder and sodium foil are assembled into a simulated sodium ion battery, and the electrochemical sodium storage performance of the battery is tested by a constant current charge/discharge method.
Advantages of the invention
The invention is based on sustainable development concepts of circular economy and green energy, the overdue donkey-hide gelatin waste drug is recycled by adopting a hard template method and a carbonization method for the first time to obtain the nitrogen/sulfur co-doped solid carbon microspheres and hollow carbon nanosphere material, waste materials are changed into valuable, a new scheme for recycling the overdue drug is provided, the secondary non-medical value of the overdue drug is fully utilized, the application feasibility of the overdue drug in a sodium ion battery is explored, and the invention has important social and environmental protection significance for developing the green energy and the circular economy.
Drawings
FIG. 1 is an SEM photograph of a black powder charge prepared in example 1;
FIG. 2 is an XRD spectrum of black powder prepared in example 2;
FIG. 3 is an EDX surface scan of black powder prepared in example 3;
fig. 4 is a charge/discharge graph of a simulated sodium ion battery prepared in example 3;
FIG. 5 is a TEM image of a black powder prepared in example 4;
FIG. 6 is an XPS survey of a black powder prepared in example 5;
fig. 7 is a charge/discharge graph of a simulated sodium ion battery prepared in example 6;
fig. 8 is a graph of the cycle stability of a simulated sodium ion battery prepared in example 7.
Detailed Description
The present invention is further illustrated by the following examples, which are not intended to limit the scope of the invention.
Example 1
A method for recovering overdue colla Corii Asini waste medicine comprises the following steps:
diluting expired donkey-hide gelatin waste medicine with water to obtain a donkey-hide gelatin solution with the concentration of 0.05g/mL, adding the donkey-hide gelatin solution into a hydrothermal reaction kettle for hydrothermal reaction for 6 hours at 180 ℃, then carrying out pyrolysis carbonization for 1 hour at 900 ℃ in a tubular furnace in nitrogen atmosphere, cooling along with the furnace, and then carrying out acid washing, water washing and drying by using dilute hydrochloric acid with the concentration of 1mol/L to obtain black powder, namely the nitrogen/sulfur co-doped solid carbon microspheres.
The morphology was measured by SEM, and as shown in fig. 1, it can be seen from fig. 1 that the sample prepared by hydrothermal carbonization had microscopically a micro-spherical morphology with a diameter of about 2 to 6 μm.
The black powder prepared in the embodiment is used as a negative electrode active material, and is assembled with a sodium foil to form a simulated sodium ion battery, and the charge/discharge performance and the cycle stability performance of the simulated sodium ion battery are tested by adopting a constant current charge/discharge method.
Example 2
A method for recovering overdue colla Corii Asini waste medicine comprises the following steps:
adding water into overdue donkey-hide gelatin waste medicines to prepare a donkey-hide gelatin solution with the concentration of 0.1g/mL, adding the donkey-hide gelatin solution into a hydrothermal reaction kettle for hydrothermal reaction for 4 hours at 190 ℃, then carrying out pyrolysis carbonization for 2 hours at 800 ℃ in a tubular furnace in a nitrogen atmosphere, cooling along with the furnace, and then carrying out acid washing, water washing and drying by using dilute hydrochloric acid with the concentration of 1mol/L to obtain black powder, namely the nitrogen/sulfur co-doped solid carbon microspheres.
By testing the XRD, as shown in fig. 2, it is understood from fig. 2 that diffraction peaks corresponding to graphite crystal planes (002) and (101) appear around 2 θ =23 ° and 2 θ =44 °, but both peaks are broadened and weak in intensity, indicating that the degree of graphitization of the carbon material is low.
The black powder prepared in the embodiment is used as a negative electrode active material, and is assembled with a sodium foil to form a simulated sodium ion battery, and the charge/discharge performance and the cycling stability performance of the simulated sodium ion battery are tested by adopting a constant current charge/discharge method.
Example 3
A method for recovering expired donkey-hide gelatin waste medicine comprises the following specific steps:
adding water into overdue donkey-hide gelatin waste medicine to prepare a donkey-hide gelatin solution with the concentration of 0.2g/mL, adding the donkey-hide gelatin solution into a hydrothermal reaction kettle for hydrothermal reaction at 200 ℃ for 3 hours, then carrying out pyrolysis carbonization at 600 ℃ for 3 hours in a tubular furnace in argon atmosphere, cooling along with the furnace, and then washing, washing and drying by using dilute hydrochloric acid with the concentration of 1mol/L to obtain black powder, namely the nitrogen/sulfur co-doped solid carbon microspheres.
The elemental composition of the sample was tested by EDX scanning, as shown in fig. 3, it can be seen from fig. 3 that the sample contains a small amount of three chemical elements of oxygen, nitrogen and sulfur in addition to the abundant carbon element, and exhibits a spherical profile corresponding to the morphology, indicating that the main component of the sample is carbon, and at the same time contains a small amount of functional groups containing nitrogen, oxygen and sulfur.
The black powder prepared in the embodiment is used as a negative electrode active material, and is assembled with a sodium foil to form a simulated sodium ion battery, and the simulated sodium ion battery is tested by a constant current charge/discharge method under the current density of 50mA/g, as shown in FIG. 4, as can be seen from FIG. 4, the first circle of discharge specific capacity is 580mAh/g, the 2 nd circle of discharge specific capacity shows irreversible capacity loss, the reversible discharge specific capacity is 378mAh/g, the 50 th circle is basically stabilized at 300mAh/g and basically coincides with the 100 th circle of discharge curve, and the nitrogen/sulfur co-doped solid carbon microsphere negative electrode has good sodium storage performance.
Example 4
A method for recovering expired donkey-hide gelatin waste medicine comprises the following specific steps:
(1) dissolving 0.6g of ferric trichloride hexahydrate, 1.2g of sodium citrate, 0.4g of urea and 0.3g of polyacrylamide in 40mL of distilled water to form a green clear solution, carrying out hydrothermal reaction in a 50mL hydrothermal reaction kettle at 200 ℃ for 12 hours, washing with water and drying to obtain a ferroferric oxide nanosphere template;
(2) and (2) adding water into overdue donkey-hide gelatin waste drugs to prepare a donkey-hide gelatin solution, wherein the concentration of the donkey-hide gelatin solution is 0.05g/mL, adding the ferroferric oxide nanospheres prepared in the step (1) according to the mass ratio of the overdue donkey-hide gelatin waste drugs to the ferroferric oxide nanospheres of 20:1, uniformly mixing, adding the mixture into a hydrothermal reaction kettle, carrying out hydrothermal reaction for 6 hours at 180 ℃, carrying out pyrolysis carbonization for 1 hour at 900 ℃ in a tubular furnace in an argon atmosphere, cooling along with the furnace, and carrying out acid washing, water washing and drying by using dilute hydrochloric acid with the concentration of 1mol/L to obtain black powder, namely the nitrogen/sulfur co-doped hollow carbon nanospheres.
The morphology of the sample is measured by TEM, as shown in FIG. 5, it can be seen from FIG. 5 that the prepared sample microscopically exhibits a hollow nanometer spherical morphology with a diameter of about 200-300 nm.
The black powder prepared in the embodiment is used as a negative electrode active material, and is assembled with a sodium foil to form a simulated sodium ion battery, and the charge/discharge performance and the cycle stability performance of the simulated sodium ion battery are tested by adopting a constant current charge/discharge method.
Example 5
A method for recovering expired donkey-hide gelatin waste medicine comprises the following specific steps:
(1) dissolving 0.6g of ferric trichloride hexahydrate, 1.2g of sodium citrate, 0.4g of urea and 0.3g of polyacrylamide in 40mL of distilled water to form a green clear solution, performing hydrothermal reaction for 12 hours at 200 ℃ in a 50mL hydrothermal reaction kettle, and washing and drying to obtain a ferroferric oxide nanosphere template;
(2) and (2) adding water into overdue donkey-hide gelatin waste drugs to prepare a donkey-hide gelatin solution, wherein the concentration of the donkey-hide gelatin solution is 0.1g/mL, adding the ferroferric oxide nanospheres prepared in the step (1) according to the mass ratio of the overdue donkey-hide gelatin waste drugs to the ferroferric oxide nanospheres of 30:1, uniformly mixing, adding the mixture into a hydrothermal reaction kettle, carrying out hydrothermal reaction for 5 hours at 190 ℃, carrying out pyrolysis carbonization for 3 hours at 600 ℃ in a tubular furnace in nitrogen atmosphere, cooling along with the furnace, and carrying out acid washing, water washing and drying by using dilute hydrochloric acid with the concentration of 1mol/L to obtain black powder, namely the nitrogen/sulfur co-doped hollow carbon nanospheres.
The XPS tests show that the element composition is shown in FIG. 6, and as can be seen from FIG. 6, the XPS full spectrum shows a strong carbon element signal peak and three weak oxygen, nitrogen and sulfur element signal peaks, which indicates that the main component of the obtained material is carbon, and in addition, nitrogen and sulfur elements are successfully doped into the carbon structure.
The black powder prepared in the embodiment is used as a negative electrode active material, and is assembled with a sodium foil to form a simulated sodium ion battery, and the charge/discharge performance and the cycling stability performance of the simulated sodium ion battery are tested by adopting a constant current charge/discharge method.
Example 6
A method for recovering overdue colla Corii Asini waste medicine comprises the following steps:
(1) dissolving 0.6g of ferric trichloride hexahydrate, 1.2g of sodium citrate, 0.4g of urea and 0.3g of polyacrylamide in 40mL of distilled water to form a green clear solution, performing hydrothermal reaction for 12 hours at 200 ℃ in a 50mL hydrothermal reaction kettle, and washing and drying to obtain a ferroferric oxide nanosphere template;
(2) adding water into overdue donkey-hide gelatin waste medicines to prepare a donkey-hide gelatin solution, wherein the concentration of the donkey-hide gelatin solution is 0.2g/mL, adding the ferroferric oxide nanospheres prepared in the step (1) according to the mass ratio of the overdue donkey-hide gelatin waste medicines to the ferroferric oxide nanospheres of 25:1, uniformly mixing, adding the mixture into a hydrothermal reaction kettle, carrying out hydrothermal reaction for 3 hours at 200 ℃, carrying out pyrolysis carbonization for 2.5 hours at 700 ℃ in a tubular furnace in nitrogen atmosphere, cooling along with the furnace, and carrying out acid washing, water washing and drying by using dilute hydrochloric acid with the concentration of 1mol/L to obtain black powder, namely the nitrogen/sulfur co-doped hollow carbon nanospheres.
The black powder prepared in the embodiment is used as a negative electrode active material, the black powder and a sodium foil are assembled to form a simulated sodium ion battery, the charge/discharge performance of the simulated sodium ion battery is tested by current densities of 0.05, 0.1, 0.2, 0.5, 1.0, 2.0 and 5.0A/g, the charge/discharge curve is shown in figure 7, and as shown in figure 7, when the current density is gradually increased, the reversible discharge specific capacity is correspondingly reduced from 365mAh/g to 322, 302, 266, 222, 174 and 98mAh/g, which shows that the nitrogen/sulfur co-doped hollow carbon nanosphere negative electrode material has good charge/discharge performance.
Example 7
A method for recovering overdue colla Corii Asini waste medicine comprises the following steps:
(1) dissolving 0.6g of ferric trichloride hexahydrate, 1.2g of sodium citrate, 0.4g of urea and 0.3g of polyacrylamide in 40mL of distilled water to form a green clear solution, performing hydrothermal reaction for 12 hours at 200 ℃ in a 50mL hydrothermal reaction kettle, and washing and drying to obtain a ferroferric oxide nanosphere template;
(2) adding water into overdue donkey-hide gelatin waste drugs to prepare a donkey-hide gelatin solution, wherein the concentration of the donkey-hide gelatin solution is 0.15g/mL, adding the ferroferric oxide nanospheres prepared in the step (1) according to the mass ratio of the overdue donkey-hide gelatin waste drugs to the ferroferric oxide nanospheres of 26:1, uniformly mixing, carrying out hydrothermal reaction on the mixture at 190 ℃ for 4 hours, carrying out pyrolysis carbonization on the mixture at 800 ℃ in a tubular furnace in nitrogen atmosphere for 2 hours, cooling along with the furnace, and carrying out acid washing, water washing and drying by using dilute salt with the concentration of 1mol/L to obtain black powder, namely the nitrogen/sulfur co-doped hollow carbon nanospheres.
The black powder prepared in the embodiment is used as a negative electrode active material, the black powder and a sodium foil are assembled to form a simulated sodium ion battery, the cycling stability of the simulated sodium ion battery is tested by current densities of 0.5A/g and 2.0A/g, as shown in fig. 8, when the battery is cycled for 500 cycles at 0.5A/g, the reversible discharge specific capacity of the battery is maintained at 266mAh/g, and when the battery is cycled for 1000 cycles at 2.0A/g, the nitrogen/sulfur co-doped hard carbon microsphere negative electrode still has the reversible discharge specific capacity of 174mAh/g, and in addition, the coulomb efficiency under two current densities is maintained at about 100%, which indicates that the nitrogen/sulfur co-doped hollow carbon nanosphere negative electrode material has good long-term cycling stability.

Claims (1)

1. A method for recycling overdue donkey-hide gelatin waste medicines is characterized in that water is added into the overdue donkey-hide gelatin waste medicines to prepare a donkey-hide gelatin solution, then ferroferric oxide nanospheres are added into the donkey-hide gelatin solution and mixed uniformly, the mixture is subjected to hydrothermal reaction at 180-200 ℃ for 3-6 hours, then the mixture is pyrolyzed and carbonized at 600-900 ℃ for 1-3 hours under an inert atmosphere, and after furnace cooling, acid washing, water washing and drying are carried out to obtain black powder which is hollow carbon sodium rice balls doped with nitrogen/sulfur;
the concentration of the donkey-hide gelatin solution is 0.05-0.2 g/mL;
the mass ratio of the expired donkey-hide gelatin waste medicine to the ferroferric oxide nanospheres is 20-30: 1.
CN201910439561.4A 2019-05-24 2019-05-24 Recovery method of overdue donkey-hide gelatin waste drug Active CN110203925B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910439561.4A CN110203925B (en) 2019-05-24 2019-05-24 Recovery method of overdue donkey-hide gelatin waste drug

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910439561.4A CN110203925B (en) 2019-05-24 2019-05-24 Recovery method of overdue donkey-hide gelatin waste drug

Publications (2)

Publication Number Publication Date
CN110203925A CN110203925A (en) 2019-09-06
CN110203925B true CN110203925B (en) 2022-07-19

Family

ID=67788429

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910439561.4A Active CN110203925B (en) 2019-05-24 2019-05-24 Recovery method of overdue donkey-hide gelatin waste drug

Country Status (1)

Country Link
CN (1) CN110203925B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117243978B (en) * 2023-10-31 2024-02-27 山东大学 Nanometer colla Corii Asini and its preparation method and application in treating aplastic anemia

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20130106591A (en) * 2012-03-20 2013-09-30 고려대학교 산학협력단 Method for preparation of hematite iron oxide with different nanostructures and hematite iron oxide thereby
CN103855366A (en) * 2012-11-28 2014-06-11 中国科学院大连化学物理研究所 Nitrogen-doped porous carbon material for lithium-air battery positive electrode
CN105129765A (en) * 2015-07-22 2015-12-09 复旦大学 Highly-ordered mesoporous carbon spheres and preparation method thereof
CN105368449A (en) * 2015-10-27 2016-03-02 山西大学 Nitrogen-doped multi-color fluorescent carbon dot and preparation method and application thereof
CN105575673A (en) * 2016-03-11 2016-05-11 北京化工大学 Preparation method of nitrogen and oxygen in-situ doped porous carbon electrode material and application thereof
CN105694356A (en) * 2016-03-14 2016-06-22 北京科技大学 Porous hollow phenolic resin nanospheres and carbon nanospheres and preparation method
CN107039191A (en) * 2017-05-09 2017-08-11 同济大学 A kind of preparation method of the hollow mesoporous Nano carbon balls of nitrogen functionalization
CN108666536A (en) * 2017-03-31 2018-10-16 北京化工大学 A kind of Cr2O3/ C compounds and its preparation method and application
CN109095451A (en) * 2018-07-23 2018-12-28 昆明理工大学 A kind of expired useless medicine vitamin B1The recoverying and utilizing method of injection

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20130106591A (en) * 2012-03-20 2013-09-30 고려대학교 산학협력단 Method for preparation of hematite iron oxide with different nanostructures and hematite iron oxide thereby
CN103855366A (en) * 2012-11-28 2014-06-11 中国科学院大连化学物理研究所 Nitrogen-doped porous carbon material for lithium-air battery positive electrode
CN105129765A (en) * 2015-07-22 2015-12-09 复旦大学 Highly-ordered mesoporous carbon spheres and preparation method thereof
CN105368449A (en) * 2015-10-27 2016-03-02 山西大学 Nitrogen-doped multi-color fluorescent carbon dot and preparation method and application thereof
CN105575673A (en) * 2016-03-11 2016-05-11 北京化工大学 Preparation method of nitrogen and oxygen in-situ doped porous carbon electrode material and application thereof
CN105694356A (en) * 2016-03-14 2016-06-22 北京科技大学 Porous hollow phenolic resin nanospheres and carbon nanospheres and preparation method
CN108666536A (en) * 2017-03-31 2018-10-16 北京化工大学 A kind of Cr2O3/ C compounds and its preparation method and application
CN107039191A (en) * 2017-05-09 2017-08-11 同济大学 A kind of preparation method of the hollow mesoporous Nano carbon balls of nitrogen functionalization
CN109095451A (en) * 2018-07-23 2018-12-28 昆明理工大学 A kind of expired useless medicine vitamin B1The recoverying and utilizing method of injection

Also Published As

Publication number Publication date
CN110203925A (en) 2019-09-06

Similar Documents

Publication Publication Date Title
Sha et al. Hierarchical carbon-coated acanthosphere-like Li4Ti5O12 microspheres for high-power lithium-ion batteries
WO2021223597A1 (en) Oxygen reduction catalyst employing graphite of negative electrode of waste battery, and preparation method therefor
CN107221665A (en) A kind of preparation method of Zinc ion battery barium oxide combination electrode material
CN105692703A (en) Lithium-enriched manganese-based cathode material, preparation method thereof, and lithium ion battery
WO2015188662A1 (en) Method of manufacturing long-life lithium-sulfur battery anode
Ding et al. Synthesis and electrochemical properties of Co3O4 nanofibers as anode materials for lithium-ion batteries
CN104201363A (en) Carbon-coated Li3VO4 lithium ion battery anode material and preparation method thereof
WO2022121400A1 (en) Coating agent, fast-charging graphite, preparation method therefor and application thereof, and battery
CN108493458B (en) High-performance echinoid nickel oxide/nickel cobaltate microsphere lithium oxygen battery positive electrode catalytic material and preparation method thereof
CN103441258B (en) The preparation method of the coated porous lithium titanate powdery of a kind of carbon
CN108172834B (en) Preparation method of low-cost graphene modified negative electrode material
CN104821238A (en) Method for preparing electrode material molybdate for super capacitor and application thereof
CN107026256B (en) Thermal battery anode material FexCo1-xS2Powder and preparation method thereof
Wu et al. Electrochemical characterization of hollow urchin-like MnO2 as high-performance cathode for aqueous zinc ion batteries
Li et al. Synthesis of porous NiO nanorods as high‐performance anode materials for lithium‐ion batteries
CN104157876A (en) Preparation method of porous carbon-tin nanocomposite material for lithium battery cathode
CN103165888B (en) Preparation method of FeF 3 nanorod with lithium intercalation activity
CN105390677A (en) Carbon self-coated semiconductor metal oxide nanosheet and graphene composite material and application thereof
CN109319757B (en) Method for preparing hollow open onion carbon lithium ion battery cathode material
Dong et al. Zn-Ce based bimetallic organic frameworks derived ZnSe/CeO2 nanoparticles encapsulated by reduced graphene oxide for enhanced sodium-ion and lithium-ion storage
CN103400969B (en) A kind of preparation method of high-performance lithium battery anode material of lithium iron phosphate/carbon composite powder
CN105428612A (en) Nano MoO2-MoSe2@SFC lithium ion battery negative electrode material and preparation method therefor
CN110203925B (en) Recovery method of overdue donkey-hide gelatin waste drug
CN107256953B (en) A kind of high-performance anode material of lithium-ion battery (VO)2P2O7The preparation method of/C composite
Wang et al. Preparation of nitrogen-doped three-dimensional hierarchical porous carbon/sulfur composite cathodes for high-performance aluminum-sulfur batteries

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