CN102531067B - Solid state method for preparing zinc ferrite nanorods - Google Patents
Solid state method for preparing zinc ferrite nanorods Download PDFInfo
- Publication number
- CN102531067B CN102531067B CN201210074265.7A CN201210074265A CN102531067B CN 102531067 B CN102531067 B CN 102531067B CN 201210074265 A CN201210074265 A CN 201210074265A CN 102531067 B CN102531067 B CN 102531067B
- Authority
- CN
- China
- Prior art keywords
- zinc ferrite
- nanorods
- solid state
- nanometer rod
- zinc
- 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.)
- Expired - Fee Related
Links
Images
Landscapes
- Compounds Of Iron (AREA)
Abstract
The invention discloses a method for preparing zinc ferrite nanorods. The method comprises the following steps of: mixing and grinding solid-state zinc acetate, ferrous chloride and oxalic acid to obtain a precursor; and calcining the precursor at 600DEG C for 2 hours to obtain one-dimensional zinc ferrite nanorods.
Description
Technical field
The present invention relates to a kind of method of preparing zinc ferrite nanometer rod by solid state reaction.
Background technology
Zinc ferrite (ZnFe
2o
4) be the composite oxides that a kind of Fe of take (III) oxide compound is main component, there is AB
2o
4spinel structure, belong to a kind of important spinel type wustite.Since 1930's, people just start it to study. at present along with people's going deep into its understanding, research in this respect has not only obtained considerable progress in theory, and as a kind of emerging functional materials, its range of application is in practice also increasingly extensive.Owing to thering is high desulfurization precision, high Sulfur capacity and high reaction activity, zinc ferrite has become the most representative complex metal oxides sweetening agent, its desulfurization rate and reproduction speed are all fast than zinc oxide, and after sulfuration, being easy to regenerate with air, steam, is a kind of efficient desulfurizing agent for high-temp gas of generally acknowledging; This compounds that it is found that oxygen vacancy the beginning of the nineties also has CO
2be reduced to the good catalytic performance .1996 of C, the researchs such as Li Xinyong find that oxygen vacancy zinc ferrite has good application prospect aspect control atmosphere pollution, can be CO in atmosphere
2, SO
2, NO
2conversion and utilization Deng material provide an effective approach, and in addition, as a kind of good catalyzer, it has been applied to the oxidative dehydrogenation of the synthetic and ethylbenzene of synthetic ammonia, F-T, butylene etc.; Because there is the features such as high resistivity, low magnetic coercive force, low eddy-current loss, high-curie temperature, so zinc ferrite is also a kind of soft magnetic material of excellent property, magnetic head materials, giant magnetic material and microwave magnetic material be can be used as, mutual inductance device, magnetic core bearing, transfer lever and magnetic recording material have been widely used at present; In absorbing material field, zinc ferrite is also a kind of important wave absorbing agent, can be applicable to the development of stealth material; The transparent inorganic pigment of ultra-fine zinc ferrite particle or a kind of excellent property, has the features such as heat-resisting, fast light and antirust; In addition it is found that it also has good gas-sensitive property; In recent years, researchist finds that zinc ferrite nanoparticle has stronger antibacterial effect, particularly evident to the sterilization effect of the bacteriums such as staphylococcus, withered grass bacterium and colibacillus.In addition, because the size of nanometer particle is less, the separation surface of its crystal grain is in neither long-range order, the height state of disarray of non-short range order again, this just makes it produce the surface effects that bulk material does not have, small-size effect, quantum effect and macro quanta tunnel effect, show that it has the physical propertiess such as the light different with conventional material, heat, electricity, magnetic, thereby arouse great concern.
The performance of material and its pattern, structure have much relations, and by the relation of research performance and pattern, we can be further from going to inquire into various reaction mechanisms, and the zinc ferrite of therefore preparing different-shape has very important effect.Wherein monodimension nanometer material receives more and more people's concern because of its various special propertys.
The preparation of zinc ferrite nanometer rod and performance study are large focal spots in current nanotechnology research field.At present, the method for preparing zinc ferrite nanometer rod mainly comprises thermal decomposition method under hydro-thermal or solvent thermal condition, in conjunction with the microemulsion method of calcining or coprecipitation method, electrospinning etc.Solid state chemistry synthesis method is not used solvent, has highly selective, high yield, simple technological process and other advantages, has become a kind of important method of nano materials.
Summary of the invention
The object of the present invention is to provide a kind of preparation method of zinc ferrite nanometer rod, do not using under the prerequisite of any tensio-active agent, utilize solid state reaction technique to prepare zinc ferrite nanometer rod by the control of calcination process temperature, for zinc ferrite nanometer rod synthetic provides a kind of simpler preparation method.
For the present invention, solid-state zinc acetate, iron protochloride and oxalic acid, as reactant, at room temperature synthesize presoma by grinding, and then thermolysis makes the monodimension nano stick being formed by nano particle accumulation.
The present invention does not use any tensio-active agent, uses process for solid phase synthesis to realize the synthetic, simple to operate, with low cost of zinc ferrite nanometer rod, and environmental friendliness, for the preparation of zinc ferrite nanometer rod provides a kind of new thinking.
accompanying drawing explanation
Fig. 1 is the powder diagram of prepared sample;
Fig. 2 is the scanning electron microscope (SEM) photograph of prepared zinc ferrite nanometer rod;
Fig. 3 is the transmission electron microscope picture of prepared zinc ferrite nanometer rod.
embodimentaccurately weigh 0.01 mol zinc acetate and 0.02 mol iron protochloride in different mortars, porphyrize mixing respectively, the oxalic acid that adds subsequently 0.03 mol porphyrize, after mixing, grind fast, along with the carrying out of grinding, mixture becomes the thick of yellow, and be attended by tart flavour and produce, continue to grind and within 40 minutes, to guarantee fully carrying out of reaction, with distilled water wash, suction filtration, naturally dry, obtain required presoma.Presoma is placed in to retort furnace, with the temperature rise rate of 5 ℃/min, rises to 600 ℃, this temperature calcining 2 hours, can obtain piling up in a certain direction by zinc ferrite nano particle the monodimension nano stick forming.
Claims (1)
1. the preparation method of a zinc ferrite nanometer rod, it is characterized in that in the situation that there is no tensio-active agent, mixed in molar ratio by solid-state zinc acetate, iron protochloride and oxalic acid with 1: 2: 3, directly grind and obtain presoma, presoma is placed in to retort furnace, temperature rise rate with 5 ℃/min rises to 600 ℃, this temperature calcining 2 hours, obtains being piled up in a certain direction by zinc ferrite nano particle the zinc ferrite nanometer rod of the one dimension forming.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210074265.7A CN102531067B (en) | 2012-03-20 | 2012-03-20 | Solid state method for preparing zinc ferrite nanorods |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210074265.7A CN102531067B (en) | 2012-03-20 | 2012-03-20 | Solid state method for preparing zinc ferrite nanorods |
Publications (2)
Publication Number | Publication Date |
---|---|
CN102531067A CN102531067A (en) | 2012-07-04 |
CN102531067B true CN102531067B (en) | 2014-04-09 |
Family
ID=46339288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201210074265.7A Expired - Fee Related CN102531067B (en) | 2012-03-20 | 2012-03-20 | Solid state method for preparing zinc ferrite nanorods |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN102531067B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103274474B (en) * | 2013-06-06 | 2015-03-11 | 吉林大学 | Rod-shaped zinc ferrite and its preparation method |
CN103601238B (en) * | 2013-11-07 | 2016-06-08 | 昆明理工大学 | A kind of microwave-assisted solid-state reaction method prepares the TiO of doping iron2The method of powder body |
CN104085930B (en) * | 2014-06-30 | 2015-11-18 | 陕西师范大学 | A kind of preparation method of bigger serface porous flake zinc ferrite |
CN106745302B (en) * | 2017-02-27 | 2018-07-27 | 陕西科技大学 | A kind of coralloid zinc ferrite powder of three-dimensional network and preparation method thereof |
CN115893504A (en) * | 2022-01-10 | 2023-04-04 | 中南大学 | Microwave-assisted preparation method of magnetic zinc ferrite |
CN116903254B (en) * | 2023-07-24 | 2024-03-08 | 吉林省一米阳光医疗器械科技有限公司 | Anti-biological adhesion functional glass ceramic material and preparation method and application thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3411215A1 (en) * | 1984-03-27 | 1985-10-10 | Basf Ag, 6700 Ludwigshafen | METHOD FOR PRODUCING TRANSPARENT GOLD-YELLOW, TEMPERATURE-STABLE TWO-PHASE PIGMENTS OF THE GENERAL FORMULA XZNO.ZNFE (DOWN ARROW) 2 (DOWN ARROW) O (DOWN ARROW) 4 (DOWN ARROW) |
CN100415653C (en) * | 2005-03-24 | 2008-09-03 | 上海大学 | Prepn process of nanometer spinel type ZnFe2O4 |
-
2012
- 2012-03-20 CN CN201210074265.7A patent/CN102531067B/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN102531067A (en) | 2012-07-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102531067B (en) | Solid state method for preparing zinc ferrite nanorods | |
Mary Jacintha et al. | Comparative studies of spinel MnFe2O4 nanostructures: structural, morphological, optical, magnetic and catalytic properties | |
Köferstein et al. | Preparation and characterization of nanosized magnesium ferrite powders by a starch-gel process and corresponding ceramics | |
Salavati-Niasari et al. | Preparation of NiO nanoparticles from metal-organic frameworks via a solid-state decomposition route | |
Ishaq et al. | Characterization and antibacterial activity of nickel ferrite doped α-alumina nanoparticle | |
Kombaiah et al. | Studies on the microwave assisted and conventional combustion synthesis of Hibiscus rosa-sinensis plant extract based ZnFe2O4 nanoparticles and their optical and magnetic properties | |
Zahid et al. | Metal ferrites and their graphene-based nanocomposites: synthesis, characterization, and applications in wastewater treatment | |
Woo et al. | Sol–gel mediated synthesis of Fe2O3 nanorods | |
Basavaraja et al. | Solvothermal synthesis and characterization of acicular α-Fe 2 O 3 nanoparticles | |
Sarangi et al. | Low temperature synthesis of single-phase α-Fe2O3 nano-powders by using simple but novel chemical methods | |
CN102190483A (en) | Three-dimensional micro-nano material composed of nano CoFe2O4 and preparation method thereof | |
Paul et al. | Facile synthesis of α-Fe2O3 nanoparticles and their catalytic activity in oxidation of benzyl alcohols with periodic acid | |
Hu et al. | ZnO/Co3O4 Porous Nanocomposites Derived from MOFs: Room‐Temperature Ferromagnetism and High Catalytic Oxidation of CO | |
CN103101980A (en) | Preparation method of multiaperture ferrite | |
Qu et al. | Fabrication of a 3D Hierarchical Flower‐Like MgO Microsphere and Its Application as Heterogeneous Catalyst | |
Cao et al. | Synthesis of Mn2O3 homogeneous core/hollow-shell structures with excellent adsorption performance | |
Lloreda-Jurado et al. | Pore morphology evolution and atom distribution of doped Fe2O3 foams developed by freeze-casting after redox cycling | |
Yang et al. | Synthesis of well-crystallized birnessite using ethylene glycol as a reducing reagent | |
Veranitisagul et al. | BaFe12O19 from thermal decomposition of bimetallic triethanolamine complex as magnetic filler for bioplastics | |
CN103553032B (en) | Method for preparing reduced graphene oxide/cerium oxide nano-bulk composite | |
Landge et al. | Solvent-free synthesis of nanoparticles | |
Ma et al. | Studies on redox H2–CO2 cycle on CoCrxFe2− xO4 | |
Drmota et al. | Synthesis of strontium hexaferrite nanoparticles prepared using co-precipitation method and microemulsion processing | |
CN108298597B (en) | Preparation method of ferrous spinel of divalent metal | |
Farghali et al. | Photocatalytic activity and magnetic properties of nanocrystallite strontium hexaferrite prepared by self-flash combustion |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20140409 Termination date: 20150320 |
|
EXPY | Termination of patent right or utility model |