CN103172124A - Method for preparing ferric oxide three-dimensional nanostructure through solid-state chemical reaction - Google Patents

Method for preparing ferric oxide three-dimensional nanostructure through solid-state chemical reaction Download PDF

Info

Publication number
CN103172124A
CN103172124A CN2013101324094A CN201310132409A CN103172124A CN 103172124 A CN103172124 A CN 103172124A CN 2013101324094 A CN2013101324094 A CN 2013101324094A CN 201310132409 A CN201310132409 A CN 201310132409A CN 103172124 A CN103172124 A CN 103172124A
Authority
CN
China
Prior art keywords
ferric oxide
dimensional nanostructure
sodium
solid state
state reaction
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
CN2013101324094A
Other languages
Chinese (zh)
Other versions
CN103172124B (en
Inventor
曹亚丽
李怡招
贾殿赠
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.)
Xinjiang University
Original Assignee
Xinjiang 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 Xinjiang University filed Critical Xinjiang University
Priority to CN201310132409.4A priority Critical patent/CN103172124B/en
Publication of CN103172124A publication Critical patent/CN103172124A/en
Application granted granted Critical
Publication of CN103172124B publication Critical patent/CN103172124B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

The invention provides a method for preparing a ferric oxide three-dimensional nanostructure through solid-state chemical reaction. The ferric oxide three-dimensional nanostructure is prepared from ferric salt or ferrous salt and a reducing agent, which are subjected to solid-state chemical reaction through by grinding or ball-milling, and then are subjected to aftertreatment. In the reaction process, a surfactant can be added to promote formation of the three-dimensional nanostructure product. The method has the advantages that the raw materials are cheap and easily available; the reaction operation is simple, little time is cost, and the volume production of nanostructures is easy; and the ferric oxide three-dimensional nanostructure prepared by the method has big specific surface area, can be applied to excellent gas sensitive, adsorbing, catalytic, electrode and carrier materials and has extensive application prospect.

Description

A kind of solid state reaction prepares the method for ferric oxide three-dimensional nanostructure
Technical field
The present invention relates to a kind of method for preparing the ferric oxide three-dimensional nanostructure by solid state reaction, belong to the nano material synthesis technical field.
Background technology
Nano-sized iron oxide (the Fe of different crystalline phases 3O 4, γ-Fe 2O 3, α-Fe 2O 3) be widely used in a plurality of fields owing to having different characteristics.Nanometer Fe 3O 4And γ-Fe 2O 3Have magnetic and good biocompatibility, can be widely used in the fields such as target drug-carrying, medical imaging, magnetic storage and catalysis; Nanometer α-Fe 2O 3Have n-N-type semiconductorN characteristic and high stability, it has important application in fields such as sensor, lithium ion battery, catalysis.As everyone knows, the pattern of nano material has material impact to its character, and the three-dimensional hierarchical structure nano-sized iron oxide that is comprised of the structure primitive (as nanoparticle, nanometer rod, nanotube, nano wire, nanometer sheet etc.) of low-dimensional nano structure causes investigator's extensive concern due to the specific surface area with superelevation and the special performance relevant to its pattern.
At present, reported that several different methods is used for the preparation of ferric oxide three-dimensional nanostructure.At first make the precursor of iron content as people such as L. Wan in the ethylene glycol that refluxes, afterwards this precursor is heat-treated at different atmosphere and temperature, obtained respectively having the nanometer Fe of three-dimensional flower-shaped structure 3O 4, nanometer γ-Fe 2O 3With nanometer α-Fe 2O 3(Advanced Materials, 18 volumes, 2426-2431 page, 2006).L. the people such as Zhang by the booster action of microwave irradiation, adds block polymer in ethylene glycol, has synthesized rose-shaped nanometer Fe by iron(ic) chloride and sodium-acetate 3O 4(The Journal of Physical Chemistry C, 114 volumes, 6237-6242 page, 2010).T. at first the people such as Fei has synthesized the FeOOH precursor by solvent-thermal method, afterwards it is calcined, and has made flower-shaped α-Fe 2O 3Hierarchy (ACS Applied Materials ﹠amp; Interfaces, 3 volumes, 4689-4694 page, 2011).Can find out, although these ferric oxide three-dimensional nanostructures have the performances such as excellent air-sensitive and absorption, but the synthetic method more complicated for the preparation of these hierarchies, reaction is higher to equipment requirements, be unfavorable for industry's enlarging production, this has limited the widespread use in practice of ferric oxide classification nanostructure.
Given this, in order to realize the more simply preparation to the ferric oxide three-dimensional nanostructure, thereby effectively be applied in every field, be necessary to develop a kind of technique simple, easy to operate, be easy to realize amplifying the preparation method of production.
Summary of the invention
The object of the present invention is to provide a kind of method for preparing the ferric oxide three-dimensional nanostructure.The method adopts the simple operation method by using cheap raw material, can synthesize the different sorts ferric oxide with three-dimensional classification nanostructure through solid state reaction.
Technical scheme of the present invention is as follows:
A kind of solid state reaction prepares the method for ferric oxide three-dimensional nanostructure, and it comprises the following steps: the ratio that molysite or ferrous salt and reductive agent are 0.1 ~ 10:1 according to mol ratio is mixed; Can add tensio-active agent, the mass ratio of molysite or ferrous salt and tensio-active agent is 0.1 ~ 10:1; Grind or ball-milling reaction 20 ~ 60 minutes; Product is water, washing with alcohol respectively, 20 ~ 120 oC air drying 0.5 ~ 24 hour; Dried sample is in air atmosphere 200 ~ 600 oC heat-treated 1 ~ 5 hour, finally obtained the ferric oxide three-dimensional nanostructure.
Molysite of the present invention or ferrous salt are one or more in ferric iron or ferrous acetate, nitrate, vitriol or muriate.Described reductive agent is the reductive agent of solid form, comprises one or more in sodium borohydride, POTASSIUM BOROHYDRIDE, azanol, oxammonium hydrochloride, sodium hypophosphite, Trisodium Citrate, sodium oxalate, hydrazonium sulfate, glucose, xitix, citric acid, oxalic acid, amino acid etc.Described tensio-active agent agent is one or more in polyoxyethylene glycol, polyvinylpyrrolidone, sodium polystyrene sulfonate, sodium lauryl sulphate, Sodium dodecylbenzene sulfonate, sodium cetanesulfonate, cetyl trimethylammonium bromide, ethylenediamine tetraacetic acid (EDTA) etc.The hierarchy of prepared ferric oxide three-dimensional nanostructure for being comprised of the ultrathin nanometer sheet comprises Fe 3O 43-D nano, structure, γ-Fe 2O 33-D nano, structure, α-Fe 2O 33-D nano, structure.
Compared with prior art, the present invention has the following advantages: take solid state reaction as the basis, adopts raw material cheap and easy to get, operate by simple grinding or ball milling, then pass through suitable thermal treatment, can make and comprise Fe 3O 4, γ-Fe 2O 3And α-Fe 2O 3In interior ferric oxide three-dimensional nanostructure.The preparation method is simple, and product yield is high, the characteristics such as is easy to realize producing in enormous quantities and all makes the present invention have very wide application prospect.
Description of drawings
Fig. 1 is the Fe of first embodiment of the invention preparation 3O 4The transmission electron microscope photo of 3-D nano, structure.
Fig. 2 is the α-Fe of second embodiment of the invention preparation 2O 3The transmission electron microscope photo of 3-D nano, structure.
Fig. 3 is the Fe of third embodiment of the invention preparation 3O 4The transmission electron microscope photo of 3-D nano, structure.
Embodiment
The present invention is further elaborated below in conjunction with specific embodiment.These embodiment are interpreted as only being used for explanation the present invention and are not used in restriction protection scope of the present invention.After the content of having read the present invention's record, based on principle of the present invention, various changes or the modification that the present invention makes fallen into claims limited range of the present invention equally.
Embodiment one:
Get the FeCl of 3 mmol 24H 2O(0.60 g) with the NaBH of 6 mmol 4(0.23 g) at room temperature carried out griding reaction 40 minutes, and product water, washing with alcohol are 60 oC air drying 5 hours obtains Fe as shown in Figure 1 3O 43-D nano, structure.
Embodiment two:
Get the FeCl of 3 mmol 24H 2O(0.60 g) with the NaBH of 6 mmol 4(0.23 g), then add 0.87 g sodium lauryl sulphate, at room temperature carrying out griding reaction 40 minutes, product water, washing with alcohol are 20 oC air drying 24 hours, dried sample are in air atmosphere 600 oC thermal treatment 1 hour obtains α-Fe as shown in Figure 2 2O 33-D nano, structure.
Embodiment three:
Get the FeCl of 3 mmol 36H 2O(0.81 g) with the NaBH of 9 mmol 4(0.34 g) at room temperature carried out griding reaction 40 minutes, and product water, washing with alcohol are 30 oC air drying 10 hours obtains Fe as shown in Figure 3 3O 43-D nano, structure.

Claims (6)

1. a solid state reaction prepares the method for ferric oxide three-dimensional nanostructure, it comprises the following steps: molysite or ferrous salt are mixed with reductive agent, can add tensio-active agent, grind or ball-milling reaction, product obtains final ferric oxide three-dimensional nanostructure after washing, drying and thermal treatment.
2. prepare the method for ferric oxide three-dimensional nanostructure according to a kind of solid state reaction claimed in claim 1, it is characterized in that: the mol ratio of molysite or ferrous salt and reductive agent is 0.1 ~ 10:1; The mass ratio of molysite or ferrous salt and tensio-active agent is 0.1 ~ 10:1; The time of grinding or ball-milling reaction is 20 ~ 60 minutes; Product is water, washing with alcohol respectively, 20 ~ 120 oC air drying 0.5 ~ 24 hour; Dried sample is in air atmosphere 200 ~ 600 oC heat-treated 1 ~ 5 hour.
3. prepare the method for ferric oxide three-dimensional nanostructure according to a kind of solid state reaction claimed in claim 1, it is characterized in that: the molysite that uses or ferrous salt are one or more in ferric iron or ferrous acetate, nitrate, vitriol or muriate.
4. prepare the method for ferric oxide three-dimensional nanostructure according to a kind of solid state reaction claimed in claim 1, it is characterized in that: the reductive agent that uses is the reductive agent of solid form, comprises one or more in sodium borohydride, POTASSIUM BOROHYDRIDE, azanol, oxammonium hydrochloride, sodium hypophosphite, Trisodium Citrate, sodium oxalate, hydrazonium sulfate, glucose, xitix, citric acid, oxalic acid, amino acid etc.
5. prepare the method for ferric oxide three-dimensional nanostructure according to a kind of solid state reaction claimed in claim 1, it is characterized in that: the tensio-active agent that uses is one or more in polyoxyethylene glycol, polyvinylpyrrolidone, sodium polystyrene sulfonate, sodium lauryl sulphate, Sodium dodecylbenzene sulfonate, sodium cetanesulfonate, cetyl trimethylammonium bromide, ethylenediamine tetraacetic acid (EDTA) etc.
6. prepare the method for ferric oxide three-dimensional nanostructure according to a kind of solid state reaction claimed in claim 1, it is characterized in that: the hierarchy of prepared ferric oxide three-dimensional nanostructure for being comprised of the ultrathin nanometer sheet comprises Fe 3O 43-D nano, structure, γ-Fe 2O 33-D nano, structure, α-Fe 2O 33-D nano, structure.
CN201310132409.4A 2013-04-17 2013-04-17 Method for preparing ferric oxide three-dimensional nanostructure through solid-state chemical reaction Expired - Fee Related CN103172124B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310132409.4A CN103172124B (en) 2013-04-17 2013-04-17 Method for preparing ferric oxide three-dimensional nanostructure through solid-state chemical reaction

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310132409.4A CN103172124B (en) 2013-04-17 2013-04-17 Method for preparing ferric oxide three-dimensional nanostructure through solid-state chemical reaction

Publications (2)

Publication Number Publication Date
CN103172124A true CN103172124A (en) 2013-06-26
CN103172124B CN103172124B (en) 2014-08-06

Family

ID=48632405

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310132409.4A Expired - Fee Related CN103172124B (en) 2013-04-17 2013-04-17 Method for preparing ferric oxide three-dimensional nanostructure through solid-state chemical reaction

Country Status (1)

Country Link
CN (1) CN103172124B (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104402067A (en) * 2014-12-05 2015-03-11 渤海大学 Method for preparing mesoporous metal oxide with large specific surface area by virtue of direct thermal decomposition
CN105762354A (en) * 2016-05-17 2016-07-13 安徽师范大学 Flower-like ferric oxide nanometer material, preparation method thereof, lithium ion battery negative pole and lithium ion battery
CN105798323A (en) * 2016-03-18 2016-07-27 西北师范大学 Method for preparing transition metal-boron alloy material with large specific surface area on ball milling-assisted interface
CN106799232A (en) * 2016-12-15 2017-06-06 浙江工业大学 Iron based ammonia synthesis catalyst of Nanoscale Iron modification prepared by a kind of solid state chemical reaction and its preparation method and application
CN106927511A (en) * 2017-04-17 2017-07-07 吉林大学 A kind of high-energy ball milling preparation method of magnetic ferroferric oxide nanometer powder
CN107311238A (en) * 2017-08-02 2017-11-03 浙江理工大学 A kind of preparation method of the hollow ferroso-ferric oxide microballoon of superparamagnetic
CN107720808A (en) * 2017-09-29 2018-02-23 张家港江苏科技大学产业技术研究院 A kind of method of low temperature preparation high-purity Nano-class Asia titanium oxide
CN110038572A (en) * 2019-04-30 2019-07-23 南开大学 A kind of α-Fe for degradable organic pollutant2O3/ Fe photochemical catalyst and preparation method thereof
CN111235625A (en) * 2020-01-21 2020-06-05 江苏理工学院 Iron oxide single crystal nano spherical particle and molten salt method synthesis method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09142847A (en) * 1995-11-22 1997-06-03 Tdk Corp Magnetitic magnetic powder, magnetic toner using the same and their production
CN1212261A (en) * 1998-04-08 1999-03-31 新疆大学 Method for preparing nanometre material by solid phase chemical reaction
CN102167291A (en) * 2011-03-18 2011-08-31 复旦大学 Method for preparing mesoporous metal oxide through pyrolysis of oxalate

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09142847A (en) * 1995-11-22 1997-06-03 Tdk Corp Magnetitic magnetic powder, magnetic toner using the same and their production
CN1212261A (en) * 1998-04-08 1999-03-31 新疆大学 Method for preparing nanometre material by solid phase chemical reaction
CN102167291A (en) * 2011-03-18 2011-08-31 复旦大学 Method for preparing mesoporous metal oxide through pyrolysis of oxalate

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
李亚东等: "室温固相法制备纳米γ-Fe2O3过程中形貌影响研究", 《信息记录材料》, vol. 8, no. 1, 31 December 2007 (2007-12-31), pages 10 - 13 *
王桂萍等: "室温固相法制备纳米Fe2O3", 《沈阳理工大学学报》, vol. 32, no. 1, 28 February 2013 (2013-02-28) *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104402067A (en) * 2014-12-05 2015-03-11 渤海大学 Method for preparing mesoporous metal oxide with large specific surface area by virtue of direct thermal decomposition
CN104402067B (en) * 2014-12-05 2016-09-28 渤海大学 A kind of method that directly high specific surface area and mesoporous metal-oxide is prepared in thermal decomposition
CN105798323B (en) * 2016-03-18 2018-04-06 西北师范大学 The method that ball milling assistant interface prepares bigger serface transition metal boron alloy material
CN105798323A (en) * 2016-03-18 2016-07-27 西北师范大学 Method for preparing transition metal-boron alloy material with large specific surface area on ball milling-assisted interface
CN105762354B (en) * 2016-05-17 2018-04-13 安徽师范大学 A kind of flower-shaped ferric oxide nano-material and preparation method thereof, negative electrode of lithium ion battery and lithium ion battery
CN105762354A (en) * 2016-05-17 2016-07-13 安徽师范大学 Flower-like ferric oxide nanometer material, preparation method thereof, lithium ion battery negative pole and lithium ion battery
CN106799232A (en) * 2016-12-15 2017-06-06 浙江工业大学 Iron based ammonia synthesis catalyst of Nanoscale Iron modification prepared by a kind of solid state chemical reaction and its preparation method and application
CN106799232B (en) * 2016-12-15 2019-08-06 浙江工业大学 A kind of iron based ammonia synthesis catalyst and its preparation method and application of the Nanoscale Iron modification of solid state chemical reaction preparation
CN106927511A (en) * 2017-04-17 2017-07-07 吉林大学 A kind of high-energy ball milling preparation method of magnetic ferroferric oxide nanometer powder
CN107311238A (en) * 2017-08-02 2017-11-03 浙江理工大学 A kind of preparation method of the hollow ferroso-ferric oxide microballoon of superparamagnetic
CN107720808A (en) * 2017-09-29 2018-02-23 张家港江苏科技大学产业技术研究院 A kind of method of low temperature preparation high-purity Nano-class Asia titanium oxide
CN110038572A (en) * 2019-04-30 2019-07-23 南开大学 A kind of α-Fe for degradable organic pollutant2O3/ Fe photochemical catalyst and preparation method thereof
CN111235625A (en) * 2020-01-21 2020-06-05 江苏理工学院 Iron oxide single crystal nano spherical particle and molten salt method synthesis method thereof
CN111235625B (en) * 2020-01-21 2022-01-25 江苏理工学院 Iron oxide single crystal nano spherical particle and molten salt method synthesis method thereof

Also Published As

Publication number Publication date
CN103172124B (en) 2014-08-06

Similar Documents

Publication Publication Date Title
CN103172124B (en) Method for preparing ferric oxide three-dimensional nanostructure through solid-state chemical reaction
Wang et al. Efficient ferrite/Co/porous carbon microwave absorbing material based on ferrite@ metal–organic framework
Zhang et al. Carbon supported PdNi alloy nanoparticles on SiO 2 nanocages with enhanced catalytic performance
Wang et al. Hydrothermal synthesis of hierarchical core–shell manganese oxide nanocomposites as efficient dye adsorbents for wastewater treatment
CN103157803B (en) A kind of solid state reaction prepares the method for Nanoalloy
Qin et al. Hydrothermal synthesis and characterization of single-crystalline α-Fe2O3nanocubes
CN102745675A (en) Preparation method of spinel-type magnetic MFe2O4/graphene composite material
Zhang et al. Active cobalt induced high catalytic performances of cobalt ferrite nanobrushes for the reduction of p-nitrophenol
CN103413921B (en) Spinel magnetic ferrite/molybdenum disulfide nanometer composite material as well as preparation method and application thereof
CN103466702B (en) Method for preparing porous bismuth oxide nano-material without template
CN104150540A (en) Heavy metal ion adsorbent ferrite hollow spheres MFe2O4
CN102826613B (en) Preparation method of graphene-based ferroferric oxide nano-composite material
CN101525157B (en) Method for preparing water-soluble ferrite nano-particle
Bao et al. Design of magnetic triple-shell hollow structural Fe3O4/FeCo/C composite microspheres with broad bandwidth and excellent electromagnetic wave absorption performance
CN102659188A (en) Magnetic ferric oxide micrometer flower material with multi-stage structure and preparation method thereof
Yin et al. Controlled synthesis of hollow α-Fe2O3 microspheres assembled with ionic liquid for enhanced visible-light photocatalytic activity
CN108941611A (en) A kind of preparation method and product of ferromagnetic nano wire
CN105741996B (en) A kind of preparation method of the superparamagnetic nano particle based on low temperature plasma
CN104003448A (en) [Alpha]-phase ferric oxide porous core-shell microspheres and controllable synthetic preparation method thereof
Zhang et al. Room-temperature synthesis of Ni nanoparticles as the absorbent used for sewage treatment
Liu et al. Modified solvothermal synthesis of magnetic microspheres with multifunctional surfactant cetyltrimethyl ammonium bromide and directly coated mesoporous shell
Jung et al. 3-D self-assembly of flower-like particles via microwave irradiation for water treatment
CN104124022A (en) Carbon-nanometer-tube-based magnetic nanometer composite material and manufacturing method thereof
CN106186046A (en) A kind of preparation method of low cost one-dimension zinc oxide nano-powder
CN108971509B (en) Preparation method of iron-nickel alloy nano material with controllable particle size

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: 20140806

Termination date: 20150417

EXPY Termination of patent right or utility model