CN110205095A - One kind being directed to the efficient wave absorbing agent and preparation method thereof of 2 ~ 18GHz frequency range - Google Patents

One kind being directed to the efficient wave absorbing agent and preparation method thereof of 2 ~ 18GHz frequency range Download PDF

Info

Publication number
CN110205095A
CN110205095A CN201910496709.8A CN201910496709A CN110205095A CN 110205095 A CN110205095 A CN 110205095A CN 201910496709 A CN201910496709 A CN 201910496709A CN 110205095 A CN110205095 A CN 110205095A
Authority
CN
China
Prior art keywords
absorbing agent
nanosphere
solution
nanometer rods
wave absorbing
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
CN201910496709.8A
Other languages
Chinese (zh)
Other versions
CN110205095B (en
Inventor
刘初阳
方罡
杨赟
彭康森
张艳婷
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.)
Nanjing University of Aeronautics and Astronautics
Original Assignee
Nanjing University of Aeronautics and Astronautics
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 Nanjing University of Aeronautics and Astronautics filed Critical Nanjing University of Aeronautics and Astronautics
Priority to CN201910496709.8A priority Critical patent/CN110205095B/en
Publication of CN110205095A publication Critical patent/CN110205095A/en
Application granted granted Critical
Publication of CN110205095B publication Critical patent/CN110205095B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00Compounds of iron
    • C01G49/02Oxides; Hydroxides
    • C01G49/08Ferroso-ferric oxide [Fe3O4]
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K9/00Screening of apparatus or components against electric or magnetic fields
    • H05K9/0073Shielding materials
    • H05K9/0081Electromagnetic shielding materials, e.g. EMI, RFI shielding
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/10Particle morphology extending in one dimension, e.g. needle-like
    • C01P2004/16Nanowires or nanorods, i.e. solid nanofibres with two nearly equal dimensions between 1-100 nanometer
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/30Particle morphology extending in three dimensions
    • C01P2004/32Spheres
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/80Particles consisting of a mixture of two or more inorganic phases

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nanotechnology (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Composite Materials (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Electromagnetism (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)
  • Soft Magnetic Materials (AREA)
  • Hard Magnetic Materials (AREA)

Abstract

The invention discloses a kind of efficient wave absorbing agent for 2~18GHz frequency range, which is nanosphere and the Fe that nanometer rods coexist3O4/ Cu compound, wherein n (Fe)/n (Cu)=27:7~27:3.The present invention utilizes the reproducibility of solvent ethylene glycol, and Fe is formed in situ3O4The compound of/Cu.And by adjusting Fe3+/Cu2+Molar ratio, control compound in simple substance Cu content.When simple substance Cu content reaches a certain level in system, is conducive to the forming core of crystal grain a direction and grows up, the form for promoting part nanosphere to coexist to nanometer rods transformation, formation nanosphere and nanometer rods.Nanosphere has bigger serface, can increase the reflection inside electromagnetic wave to enhance the absorption to electromagnetic wave;And nanometer rods are then conducive to the transmission of electronics, and material internal is made to form conductive network easily to enhance dielectric loss.Wave absorbing agent of the invention, when with a thickness of~2mm, the reachable -53.43dB of RL is lost in most strong reflection, while maximum effectively Absorber Bandwidth is up to 5.84GHz.The Fe that this nanosphere and nanometer rods coexist3O4The bandwidth of/Cu composite wave-absorbing agent is better than current most of Fe3O4Based composites.

Description

A kind of efficient wave absorbing agent and preparation method thereof for 2~18GHz frequency range
Technical field
The invention belongs to absorbing material technical fields, and in particular to a kind of efficient wave absorbing agent for 2~18GHz frequency range and Preparation method.
Background technique
The high speed development of current electromagnetic wave technology, electronic equipment is ubiquitous in people's lives, brings a large amount of Electromagnetic interference and pollution seriously threaten the health of people;And militarily, modern war is exactly an information war, For the catbird seat occupied in war, the stealth technology for improving weaponry is extremely urgent.It is exactly currently with most 2~18GHz of centimeter wave, therefore developing the efficient wave absorbing agent of a kind of " thin, light, wide, strong " in the wave band is one extremely important Task.
Fe3O4It is in ferrimagnetism, since dielectric loss with higher and magnetic loss are extensive with inverse spinel structure Be applied to absorbing material, but single-phase Fe3O4The problems such as absorbing material thickness is larger and stability is poor is not able to satisfy existing For the requirement of absorbing material.Therefore, Fe3O4The compound absorbing material of base becomes the emphasis of people's research.It is well known that in addition to Outside the intrinsic properties of material itself, pattern is also an important parameter for influencing Absorbing Materials.The spherical pattern of nanometer has Helping to improve electromagnetic wave by increasing specific surface area enhances the absorption to electromagnetic wave in internal multiple reflections;And nano bar-shape Pattern is then conducive to the transmission of electronics, and material internal is made to form conductive network easily to enhance dielectric loss.Using nanosphere and receive The Fe that rice stick coexists3O4/ Cu compound is as absorbing material, on the one hand, the pattern that nanosphere and nanometer rods coexist combines The above nanosphere and nanometer rods advantage.On the other hand in addition to can use Fe3O4Itself dielectric loss and magnetic loss and Cu's High conductivity is lost outside electromagnetic wave, can also utilize Fe3O4The space charge of heterogeneous interface gathers the interface to be formed between Cu Loss is to enhance the absorption to electromagnetic wave.Absorbing property is improved by the combination of more loss mechanisms.
However, to obtain nanosphere and Fe that nanometer rods coexist3O4/ Cu compound, the Fe for needing accurate control to be added3+/ Cu2+Molar ratio.In fact, in forming process, if Fe3+/Cu2+Molar ratio is excessive, Cu2+Fe can mainly be entered3O4Lattice in To replace Fe2+Ion forms single-phase Cu2+Adulterate Fe3O4.Only work as Fe3+/Cu2+When molar ratio is reduced to OK range, into Enter Fe3O4Cu2+It reaches capacity, can just start to generate simple substance Cu, obtain Fe3O4/ Cu composite material.Also, when Cu simple substance is in body When reaching a certain concentration in system, Fe can be become3O4Nucleation point, be conducive to crystal grain a direction forming core and grow up, promote part Nanosphere changes to nanometer rods, the Fe that finally acquisition nanosphere and nanometer rods coexist3O4/ Cu compound.And if Fe3+/Cu2+Mole Magnetic phase Fe than too small, in system3O4Content is very few, can cause being greatly reduced for system magnetic loss, seriously destroy impedance matching Situation will be unfavorable for the raising of absorbing property.Therefore, excellent absorbing property is obtained in 2~18GHz frequency range, be critical to essence The really Fe that control is added3+/Cu2+Molar ratio.
Summary of the invention
The purpose of the present invention is to provide it is a kind of for 2~18GHz frequency range have efficient wave-sucking performance wave absorbing agent and its Preparation method.
The present invention is directed to the efficient wave absorbing agent of 2~18GHz frequency range, has following microscopic appearance and chemical component: nanosphere The Fe coexisted with nanometer rods3O4/ Cu compound, wherein n (Fe)/n (Cu)=23:7~27:3.
The preparation method of efficient wave absorbing agent for 2~18GHz frequency range of the invention, comprising the following steps:
1) (3-x): x in molar ratio, x=0.3~0.7 weigh iron chloride and copper chloride is placed in beaker, by 60~ The ethylene glycol of 100ml is added in beaker and stirs 5~15min, and sufficiently dissolution obtains solution A;Wherein, iron chloride and copper chloride Total mol concentration is 1.5~2.5mol/L.
2) 7.2~8.0g sodium acetate is added into solution A, and stirs 0.5~1.5h and obtains solution B;Solution B is packed into In 100ml reaction kettle, it is placed in baking oven, keep the temperature 18 at 180~220 DEG C~for 24 hours, the final solution for obtaining layering;
3) supernatant liquor is gone, collects the black powder of reaction kettle bottom, it is repeatedly clear with deionized water and dehydrated alcohol It washes, and dry 6~12h in 60~80 DEG C of vacuum oven, obtains Fe3O4/ Cu powder.
Compared with the background art, the invention has the advantages that:
By designing chemical composition, Fe is controlled3+/Cu2+Molar ratio, obtain the Fe that nanosphere and nanometer rods coexist3O4/Cu Compound.Increase absorption of the reflection enhancement to electromagnetic wave inside electromagnetic wave, nanometer rods structure using the bigger serface of nanosphere The good conductive network built enhances dielectric loss, Fe3O4With Cu itself respectively strong natural resonance loss and high conductivity and Interfacial polarization between them, the collective effect of these more loss mechanisms improve the absorbing property of 2~18GHz frequency range.This hair Bright Fe3O4/ Cu composite absorber is when with a thickness of~2mm, the strongest reachable -53.43dB of reflection loss RL, and maximum has Absorber Bandwidth is imitated up to 5.84GHz.The Fe that this nanosphere and nanometer rods coexist3O4The composite material of base absorbs bandwidth and is better than mesh Preceding most of Fe3O4Based composites are expected to have application back well in the electro-magnetic wave absorption field of 2~18GHz frequency range Scape.
Detailed description of the invention
Fig. 1 is the pure Fe that embodiment 1 obtains3O4The SEM shape appearance figure and 2~18GHz absorbing property of wave absorbing agent are with frequency Variation relation curve;
Fig. 2 is the Fe that embodiment 2 obtains3O4The SEM shape appearance figure of/Cu [n (Fe)/n (Cu)=29:1] composite wave-absorbing agent and 2~18GHz absorbing property with frequency variation relation curve;
Fig. 3 is the Fe that embodiment 3 obtains3O4The SEM shape appearance figure of/Cu [n (Fe)/n (Cu)=27:3] composite wave-absorbing agent and 2~18GHz absorbing property with frequency variation relation curve;
Fig. 4 is the Fe that embodiment 4 obtains3O4The SEM shape appearance figure of/Cu [n (Fe)/n (Cu)=25:5] composite wave-absorbing agent and 2~18GHz absorbing property with frequency variation relation curve;
Fig. 5 is the Fe that embodiment 5 obtains3O4The SEM shape appearance figure of/Cu [n (Fe)/n (Cu)=23:7] composite wave-absorbing agent and 2~18GHz absorbing property with frequency variation relation curve.
Specific embodiment
The present invention is further illustrated with reference to embodiments.
Embodiment 1:
1) it weighs 0.01mol iron chloride to be placed in beaker, the ethylene glycol of 80ml is added in beaker and is stirred 10min, Sufficiently dissolution obtains solution A;
2) 7.2g sodium acetate is added into solution A, and stirs 0.5h and obtains solution B;
3) solution B is fitted into 100ml reaction kettle, is placed in baking oven, keep the temperature 20h at 200 DEG C, be finally layered Solution;
4) supernatant liquor is gone, collects the black powder of reaction kettle bottom, it is repeatedly clear with deionized water and dehydrated alcohol It washes three times, and the dry 6h in 60 DEG C of vacuum oven, obtains pure Fe3O4Powder.
The absorbing property of 2~18GHz frequency range radar absorbent material made from this example is same using Agilent vector network analyzer The test of axis method of testing.It is when test that absorbing material powder and solid paraffin 7:3 in mass ratio of the invention is uniformly mixed at 80 DEG C It is tested after conjunction.
Fig. 1 is the pure Fe of 2~18GHz radar absorbent material that embodiment 1 obtains3O4SEM shape appearance figure and absorbing property with frequency The variation relation curve of rate;It can be seen that when with a thickness of 3.45mm, RL < -10dB frequency range covering 5.68~ 8.64GHz, Effective frequency width of absorption reaches 2.96GHz, while most strong absworption peak reaches -41.79dB.
Embodiment 2:
1) 2.9:0.1 weighs iron chloride in molar ratio and copper chloride is placed in beaker, and the ethylene glycol of 80ml is added and is burnt In cup and 10min is stirred, sufficiently dissolution obtains solution A;
2) 7.2g sodium acetate is added into solution A, and stirs 0.5h and obtains solution B;
3) solution B is fitted into 100ml reaction kettle, is placed in baking oven, keep the temperature 20h at 200 DEG C, be finally layered Solution;
4) supernatant liquor is gone, collects the black powder of reaction kettle bottom, it is repeatedly clear with deionized water and dehydrated alcohol It washes three times, and the dry 6h in 60 DEG C of vacuum oven, obtains Fe3O4/ Cu powder.
The absorbing property of 2~18GHz frequency range radar absorbent material made from this example is same using Agilent vector network analyzer The test of axis method of testing.It is when test that absorbing material powder and solid paraffin 7:3 in mass ratio of the invention is uniformly mixed at 80 DEG C It is tested after conjunction.
Fig. 2 is 2~18GHz radar absorbent material Fe that embodiment 2 obtains3O4The SEM shape appearance figure and absorbing property of/Cu with The variation relation curve of frequency;It can be seen that when with a thickness of 2.25mm, RL < -10dB frequency range covering 13.20~ 17.20GHz, Effective frequency width of absorption reaches 4.00GHz, while most strong absworption peak reaches -20.09dB.
Embodiment 3:
1) 2.7:0.3 weighs iron chloride in molar ratio and copper chloride is placed in beaker, and the ethylene glycol of 80ml is added and is burnt In cup and 10min is stirred, sufficiently dissolution obtains solution A;
2) 7.2g sodium acetate is added into solution A, and stirs 0.5h and obtains solution B;
3) solution B is fitted into 100ml reaction kettle, is placed in baking oven, kept the temperature at 180 DEG C for 24 hours, be finally layered Solution;
4) supernatant liquor is gone, collects the black powder of reaction kettle bottom, it is repeatedly clear with deionized water and dehydrated alcohol It washes three times, and the dry 6h in 60 DEG C of vacuum oven, obtains Fe3O4/ Cu powder.
The absorbing property of 2~18GHz frequency range radar absorbent material made from this example is same using Agilent vector network analyzer The test of axis method of testing.It is when test that absorbing material powder and solid paraffin 7:3 in mass ratio of the invention is uniformly mixed at 80 DEG C It is tested after conjunction.
Fig. 3 is 2~18GHz radar absorbent material Fe that embodiment 3 obtains3O4The SEM shape appearance figure and absorbing property of/Cu with The variation relation curve of frequency;It can be seen that when with a thickness of 2.25mm, RL < -10dB frequency range covering 12.40~ 17.36GHz, Effective frequency width of absorption reaches 4.96GHz, while most strong absworption peak reaches -49.76dB.
Embodiment 4:
1) 2.5:0.5 weighs iron chloride in molar ratio and copper chloride is placed in beaker, and the ethylene glycol of 80ml is added and is burnt In cup and 10min is stirred, sufficiently dissolution obtains solution A;
2) 7.5g sodium acetate is added into solution A, and stirs 1.0h and obtains solution B;
3) solution B is fitted into 100ml reaction kettle, is placed in baking oven, keep the temperature 22h at 200 DEG C, be finally layered Solution;
4) supernatant liquor is gone, collects the black powder of reaction kettle bottom, it is repeatedly clear with deionized water and dehydrated alcohol It washes three times, and the dry 9h in 60 DEG C of vacuum oven, obtains Fe3O4/ Cu powder.
The absorbing property of 2~18GHz frequency range radar absorbent material made from this example is same using Agilent vector network analyzer The test of axis method of testing.It is when test that absorbing material powder and solid paraffin 7:3 in mass ratio of the invention is uniformly mixed at 80 DEG C It is tested after conjunction.
Fig. 4 is 2~18GHz radar absorbent material Fe that embodiment 4 obtains3O4The SEM shape appearance figure and absorbing property of/Cu with The variation relation curve of frequency;It can be seen that when with a thickness of 1.9mm, RL < -10dB frequency range covering 11.60~ 17.44GHz, Effective frequency width of absorption reaches 5.84GHz, while most strong absworption peak reaches -53.43dB.
Embodiment 5:
1) 2.3:0.7 weighs iron chloride in molar ratio and copper chloride is placed in beaker, and the ethylene glycol of 80ml is added and is burnt In cup and 10min is stirred, sufficiently dissolution obtains solution A;
2) 8g sodium acetate is added into solution A, and stirs 1.5h and obtains solution B;
3) solution B is fitted into 100ml reaction kettle, is placed in baking oven, kept the temperature at 180 DEG C for 24 hours, be finally layered Solution;
4) supernatant liquor is gone, collects the black powder of reaction kettle bottom, it is repeatedly clear with deionized water and dehydrated alcohol It washes three times, and the dry 12h in 60 DEG C of vacuum oven, obtains Fe3O4/ Cu powder.
The absorbing property of 2~18GHz frequency range radar absorbent material made from this example is same using Agilent vector network analyzer The test of axis method of testing.It is when test that absorbing material powder and solid paraffin 7:3 in mass ratio of the invention is uniformly mixed at 80 DEG C It is tested after conjunction.
Fig. 5 is 2~18GHz radar absorbent material Fe that embodiment 5 obtains3O4The SEM shape appearance figure and absorbing property of/Cu with The variation relation curve of frequency;It can be seen that when with a thickness of 1.7mm, RL < -10dB frequency range covering 13.44~ 18.00GHz, Effective frequency width of absorption reaches 4.56+GHz, while most strong absworption peak reaches -40.434dB.

Claims (2)

1. a kind of efficient wave absorbing agent for 2~18 ghz bands, characterized in that the wave absorbing agent has following microscopic appearance and change It studies point: the Fe that nanosphere and nanometer rods coexist3O4/ Cu compound, wherein n (Fe)/n (Cu)=23:7~27:3.
2. the preparation method of the efficient wave absorbing agent described in claim 1 for being directed to 2~18 ghz bands, which is characterized in that step It is as follows:
1) (3-x): x in molar ratio, x=0.3~0.7 weigh iron chloride and copper chloride is placed in beaker, by 60~100ml's Ethylene glycol is added in beaker and stirs 5~15min, and sufficiently dissolution obtains solution A;Wherein, the total moles of iron chloride and copper chloride Concentration is 1.5~2.5mol/L;
2) 7.2~8.0g sodium acetate is added into solution A, and stirs 0.5~1.5h and obtains solution B;Solution B is packed into 100ml In reaction kettle, it is placed in baking oven, keep the temperature 18 at 180~220 DEG C~for 24 hours, the final solution for obtaining layering;
3) supernatant liquor is gone, collects the black powder of reaction kettle bottom, is cleaned repeatedly with deionized water and dehydrated alcohol, and Dry 6~12h, obtains Fe in 60~80 DEG C of vacuum oven3O4/ Cu powder.
CN201910496709.8A 2019-06-10 2019-06-10 Efficient wave absorbing agent for 2-18 GHz frequency band and preparation method thereof Active CN110205095B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910496709.8A CN110205095B (en) 2019-06-10 2019-06-10 Efficient wave absorbing agent for 2-18 GHz frequency band and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910496709.8A CN110205095B (en) 2019-06-10 2019-06-10 Efficient wave absorbing agent for 2-18 GHz frequency band and preparation method thereof

Publications (2)

Publication Number Publication Date
CN110205095A true CN110205095A (en) 2019-09-06
CN110205095B CN110205095B (en) 2020-10-16

Family

ID=67791704

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910496709.8A Active CN110205095B (en) 2019-06-10 2019-06-10 Efficient wave absorbing agent for 2-18 GHz frequency band and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110205095B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113707464A (en) * 2021-08-27 2021-11-26 西北大学 Nano iron oxide/copper composite material and preparation method and application thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101417822A (en) * 2008-11-24 2009-04-29 中国科学院长春应用化学研究所 Method for preparing super paramagnetic mesoporous ferriferrous oxide nano particle
CN101703936A (en) * 2009-11-30 2010-05-12 上海交通大学 Magnetic nano catalyst and preparation method thereof
CN101717122A (en) * 2009-12-04 2010-06-02 华中师范大学 Method for preparing ferroferric oxide nano-piece through microwave method
CN101844963A (en) * 2010-02-04 2010-09-29 广东理文化工研发有限公司 Method for preparing perfluoroalkyl iodide
CN103263886A (en) * 2013-06-06 2013-08-28 湖北大学 Hydrothermal preparation method and application of magnetic ferroferric oxide nanochain
CN104437344A (en) * 2014-10-13 2015-03-25 中南大学 Copper doped composite magnetic nano-material and preparation and application thereof
CN106040240A (en) * 2016-05-27 2016-10-26 中南民族大学 Nanometer Cu0/Fe3O4 compound, method for preparing same and application of nanometer Cu0/Fe3O4 compound to treating organic wastewater by means of catalytically activating molecular oxygen
CN107519873A (en) * 2017-07-31 2017-12-29 江苏大学 A kind of preparation method and application of Cu based metal catalysts

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101417822A (en) * 2008-11-24 2009-04-29 中国科学院长春应用化学研究所 Method for preparing super paramagnetic mesoporous ferriferrous oxide nano particle
CN101703936A (en) * 2009-11-30 2010-05-12 上海交通大学 Magnetic nano catalyst and preparation method thereof
CN101717122A (en) * 2009-12-04 2010-06-02 华中师范大学 Method for preparing ferroferric oxide nano-piece through microwave method
CN101844963A (en) * 2010-02-04 2010-09-29 广东理文化工研发有限公司 Method for preparing perfluoroalkyl iodide
CN103263886A (en) * 2013-06-06 2013-08-28 湖北大学 Hydrothermal preparation method and application of magnetic ferroferric oxide nanochain
CN104437344A (en) * 2014-10-13 2015-03-25 中南大学 Copper doped composite magnetic nano-material and preparation and application thereof
CN106040240A (en) * 2016-05-27 2016-10-26 中南民族大学 Nanometer Cu0/Fe3O4 compound, method for preparing same and application of nanometer Cu0/Fe3O4 compound to treating organic wastewater by means of catalytically activating molecular oxygen
CN107519873A (en) * 2017-07-31 2017-12-29 江苏大学 A kind of preparation method and application of Cu based metal catalysts

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113707464A (en) * 2021-08-27 2021-11-26 西北大学 Nano iron oxide/copper composite material and preparation method and application thereof

Also Published As

Publication number Publication date
CN110205095B (en) 2020-10-16

Similar Documents

Publication Publication Date Title
Chen et al. Interconnected magnetic carbon@ NixCo1-xFe2O4 nanospheres with core–shell structure: An efficient and thin electromagnetic wave absorber
CN113025271B (en) Ti 3 C 2 T x Preparation method of MXene @ ZnO composite wave-absorbing material
CN112292015B (en) MXene/PPy composite wave absorbing agent and preparation method thereof
CN108795379A (en) A kind of preparation method of three-dimensional netted multi-walled carbon nanotube/Ni ferrite composite wave-suction material
CN104099062B (en) Compounded wave-absorbing material of grapheme/four-pin zinc oxide whisker and preparation method thereof
CN113388254B (en) MoCo bimetal sulfide/carbon fiber composite material and preparation method thereof
CN103467079A (en) Preparation method for grapheme/Ni0.8Zn0.2Ce0.06Fe1.94O4 nano wave-absorbing material
CN112456562A (en) Ferrite-based composite material and preparation method and application thereof
CN112442334A (en) Barium ferrite carbon sphere composite wave-absorbing material and preparation method thereof
CN112752496A (en) Hollow nitrogen-doped nickel oxide/nickel/carbon composite material, preparation method and application
CN112341992A (en) Composite wave-absorbing material and preparation method and application thereof
CN106350003A (en) Preparation method of porous graphene/ferroferric oxide composite absorbing material
CN110205095A (en) One kind being directed to the efficient wave absorbing agent and preparation method thereof of 2 ~ 18GHz frequency range
CN113999651A (en) Nickel-cobalt dual-ligand metal-organic framework material and preparation method and application thereof
CN102807840B (en) Preparation method for nanometer Fe3O4-SrFe12O19 compound wave absorption material
CN110340376B (en) Flower-shaped nickel wire wave-absorbing material and preparation method thereof
CN100429023C (en) Magnetic micro powder and method for making same
CN114727575A (en) Layered multi-loss mechanism wave-absorbing material and preparation method thereof
CN112875768B (en) One-dimensional coralliform NiS/Ni3S4@PPy@MoS2Wave absorber, preparation method and application
CN110586933B (en) High-temperature-resistant modification method of zirconium dioxide coated FeCo absorbent
CN114956192A (en) Lanthanum-cobalt co-doped barium ferrite dual-waveband wave-absorbing powder material and preparation method thereof
CN115491178B (en) CoFe (CoFe) 2 O 4 Preparation and application of mesoporous carbon core-shell wave-absorbing material
CN110157378B (en) Walnut shell biomass C/Fe3O4Preparation method of/Cu microwave absorbing material
CN115505910B (en) Magnetic metal @ SiC wave-absorbing powder and preparation method thereof
CN113104850B (en) Preparation method of double-loss type electromagnetic wave-absorbing material and electromagnetic wave-absorbing material

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