CN1799990A - Preparation method of nanometer metal oxide and composite metal oxide - Google Patents

Preparation method of nanometer metal oxide and composite metal oxide Download PDF

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CN1799990A
CN1799990A CN 200510126625 CN200510126625A CN1799990A CN 1799990 A CN1799990 A CN 1799990A CN 200510126625 CN200510126625 CN 200510126625 CN 200510126625 A CN200510126625 A CN 200510126625A CN 1799990 A CN1799990 A CN 1799990A
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urea
metal oxide
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CN100368281C (en
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李国军
孙占如
任瑞铭
陈春焕
赵红
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Dalian Jiaotong University
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Abstract

The invention discloses a making method of nanometer metal oxide and composite metal oxide, which is characterized by the following: combining the macromolecular network gelatinization with micro-area deposition course; obtaining nanometer grade, even particle, narrow distribution, little agglomerating, controllable particle diameter spherical high pure metal oxide and or composite metal oxide particle; polymerizing small molecular organics into netted macromolecule at original position; making the soluble metal salt and urea solution into wet gel; hydrolyzing the urea at certain temperature in the steam; proceeding deposition reaction in the three-dimensional network mini-area; forming nanometer powder body through heat treating.

Description

The preparation method of a kind of nano-metal-oxide and complex metal oxides
Technical field
The present invention relates to nanotechnology, relate in particular to the preparation method of a kind of nano-metal-oxide and complex metal oxides.
Background technology
Nanotechnology is the crystallization of 20th century development in science and technology, is one of three big science and technology of 21 century.The preparation of nano-powder and complete processing and applied research are the important branch fields of nanotechnology, have contained each crossing domains such as chemical industry, material, electronics, military affairs, manufacturing, industry, and the aspects such as social concern that caused by nanotechnology.Nano-powder be meant grain size at 1nm to the nanoparticle between the 100nm.Owing to itself have surface effects, small-size effect, quantum size effect and macroscopical tunnel effect etc., make it show the property that is different from conventional material at aspects such as light, electricity, magnetic, mechanics and catalysis.Nano-metal-oxide and composite metal oxide powder as an important class material in chemical industry, electronics, metallurgy, aerospace, life. fields such as thing and medical science have broad application prospects.
The preparation method that nano-metal-oxide and complex metal oxides are commonly used is an alkaline chemical precipitation method in the soluble metal salts solution, through filtration, dry, high-temperature heat treatment, obtains nano-powder.As publication number is the patent document disclosed " composite oxide semiconductor preparation of nanomaterials " of CN1622283A, and this method technology is simple, easily suitability for industrialized production.But well-known, because the precipitated product that this method generates is gluey oxyhydroxide mostly, filtration time is long, has correspondingly increased the production cycle; Moreover easily form hydrogen bond between the throw out, and when filtration, drying, pyroprocessing, easily cause powder granule to reunite, grow up, be difficult to obtain the powder of uniform particles, good dispersity, hard aggregation-free.Though (Liu Jun etc., vacuum freeze-drying method prepare the research of nano aluminium oxide ceramics powder to some scholar, vacuum, 2004,41 (4): 80-83; Cao Aihong, the precipitator method prepare TiO 2The research of nano-powder and microwave drying, Henan chemical industry, 2002 (6): 9-11) adopt ways such as lyophilize, microwave drying to reduce reunion, but these measures need task equipment, and output is little, lacks practicality in industrial production.
Sol-gel method is a lot of method for preparing nano-metal-oxide and composite metal oxide powder of another research.It mainly adopts the organism of metal that hydrolysis formation colloidal sol takes place in the aqueous solution, and then polymerization reaction take place generates the gel with certain space structure, through super-dry, thermal treatment at a certain temperature obtains nano-metal-oxide and composite metal oxide powder then.As (O.Varnier etc., Sol-gelsynthesis of magnesium aluminum spinel from a heterometallic alkoxide, Mat Res Bull, 1994,29:479-488; ).But as we all know, this kind method shortcoming is that cost of material is relatively more expensive, and the production cycle is long.
People such as A.Douy (A.Douy et al, The polyacrylamide gel:A novel route to ceramicand glassy oxide powders, Materials Research Bulletin, 1989,24 (9): 1119-1126) and people (Wu Yanchun etc. such as Wu Yanchun, the chemical soft of nano NiO ultrafine powder synthesized, HeFei University of Technology's journal (natural science edition), 2003,26 (3): 404-406) with nitrate be raw material, in its aqueous solution, add acrylamide monomer, N, N '-methylene-bisacrylamide is as linking agent, obtain polyacrylamide-gel in action of evocating, dry postheat treatment obtains nano composite metal oxide and metal-oxide powder.Because the grid that forms can not stop metal ion to move in drying process, powder granule is reunited still relatively more serious.
(Zhao Jiupeng etc., organic gel method low temperature synthesizes Sr to people such as Zhao Jiupeng xBa 1-xNb 2O 5Powder, Journal of Inorganic Materials, 2004,19 (1): 75-80) and people (Zhang Bangqiang etc. such as Zhang Bangqiang, organic gel method prepares doping chromic acid lanthanum nano-powder, silicate journal, 2005,33 (4): 447-451) utilize organic gel method to synthesize nano-metal-oxide and composite oxide of metal powder, it is raw material that this method adopts metal nitrate, in its aqueous solution, add citric acid as complexing agent and ethylene glycol as linking agent, water-bath gel after drying, in low-temperature ignition, obtain nano-powder at last.This method gel, time of drying are long, and burning is violent, and powder granule size and pattern are difficult to control.
Summary of the invention
In view of the existing in prior technology shortcoming and defect, the object of the present invention is to provide a kind of preparation high quality nano level, epigranular, narrowly distributing, it is few to reunite, the method for size-controllable spherical metal oxide or composite metal oxide powder.
Technical solution of the present invention is achieved in that
The preparation method of a kind of nano-metal-oxide and complex metal oxides, it is characterized in that it combines polyacrylamide-gelization with the microcell precipitation process, preparation nano-metal-oxide and complex metal oxides, its technological process is as follows: one or more soluble metallic salt and urea are dissolved in the deionized water, stir, add monomer and linking agent again, be made into mixing solutions, and place and stir the initiator that the back adds gelation on the agitator, polymerization reaction take place forms macromolecule network wet gel body in 35-75 ℃ of temperature range then, it is heated in 80-120 ℃ of saturated steam, urea generation hydrolysis, form precipitation with the metal ion in the network microcell, last, according to the difference of final generation product, the wet gel of gained is directly calcined, making particle diameter is 10~100 nanometers, epigranular, size-controllable spherical metal oxide and composite metal oxide powder;
Described soluble metallic salt is meant to generate sedimentary soluble metal nitrate or vitriol with the hydrolysate of urea that its consumption calculates by the content of each metal ion species in the desired final product; Urea is as the precipitation agent of microcell precipitin reaction, and its consumption is 1.2~3 times of mole numbers pressing the effective metal total ion concentration of reaction ratio calculating; Monomer is selected acrylamide for use, and linking agent is selected N for use, and N '-methylene-bisacrylamide, both consumptions are 10: 1~3: 1 by weight; The initiator of gelation is selected ammonium persulphate for use, and its adding proportion is 10~20wt% ammonium persulfate solution that every 100ml mixing solutions drips 2~1ml.
Described mixing solutions can adopt one or more soluble metallic salt and urea is dissolved in and contain acrylamide monomer and N, and is formulated in the aqueous solution of N '-methylene-bisacrylamide.
Described soluble metallic salt employing can generate sedimentary soluble metal nitrate with the hydrolysate of urea preferable, and it forms corresponding ammonium nitrate by product when forming precipitation by metallic ion in the microcell precipitation process.
Described heat treated concrete calcining temperature and time need to decide according to the final product that generates, and residual byproduct of reaction C and N are eliminated in thermal treatment when obtaining required nano-powder.
Described various raw material comprises soluble metal nitrate, urea, acrylamide monomer, N, N '-methylene-bisacrylamide, ammonium persulphate, and its purity is more than the chemical pure.
The present invention proposes a kind of polymer-network gel method and the microcell precipitator method are combined and prepare the method for nanosize metal oxide and complex metal oxides.It is utilize small organic molecule under certain condition in-situ polymerization reticulate polymer, the aqueous solution that will contain soluble metallic salt and urea directly becomes wet gel, make hydrolysis of urea in the saturated steam at a certain temperature then, in the three-dimensional network microcell precipitin reaction taking place, obtains nano-powder through Overheating Treatment at last.Soluble metallic salt is introduced required metal ion in the final product; Urea is the precipitation agent as the microcell precipitin reaction; Small organic molecule, as acrylamide monomer, N, N '-methylene-bisacrylamide is as forming the high molecular raw material of network.Heat treated purpose is to obtain Single Phase Metal oxide compound or complex metal oxides in order to guarantee, and eliminates residual C and N.Thermal treatment temp is decided according to the product of ultimate demand.Because the effect of grid, being deposited in of generation is not easy to pass grid in the heat treatment process, the difficult reunion, thereby obtain particle tiny, reunite less, the powder of good dispersity.
With the powder that method provided by the present invention obtains, synthesis temperature is lower relatively, and powder granularity is little, and the sintering activity height is suitable for preparing high performance agglomerated material; Simultaneously, this method have technology simple, fast, cost is low, process is easy to control, be easy to advantage such as suitability for industrialized production.
Description of drawings
2 in accompanying drawing of the present invention, wherein
Fig. 1 is the XRD figure spectrum of embodiment 1 gained powder;
Fig. 2 is the transmission electron microscope photo of embodiment 1 gained powder.
Wherein, Fig. 2 is a Figure of abstract of the present invention.
Embodiment
Embodiment 1
Get 7.503g Al (NO 3) 39H 2O, 2.564gMg (NO 3) 26H 2O and 4.805g urea are dissolved in 80ml and contain the 5wt% acrylamide, acrylamide and N, N '-methylene-bisacrylamide mass ratio is in 5: 1 the mixing solutions, and then drip the ammonium persulfate solution of 0.8ml 20wt%, after stirring, be placed in 63 ℃ the water-bath heating until forming gel.Wet gel was placed in 110 ℃ the saturated steam heating 2 hours, and placed it in then in the box-type furnace, be warming up to 1000 ℃ of calcining 2h, promptly obtain white, particle diameter is the MgAl of 40~50nm 2O 4Nano-powder.As Fig. 1 is the X R D collection of illustrative plates of product, shows that product is single magnesium-aluminium spinel phase; Fig. 2 is the transmission electron microscope photo of prepared powder, shows that powder granule is a nano level, epigranular, and it is less to reunite.
Embodiment 2 and embodiment 3 compare with embodiment 1, and technological process is identical, and related parameter changes as shown in the table:
Figure A20051012662500061

Claims (5)

1, the preparation method of a kind of nano-metal-oxide and complex metal oxides, it is characterized in that it combines polyacrylamide-gelization with the microcell precipitation process, preparation nano-metal-oxide and complex metal oxides, its technological process is as follows: one or more soluble metallic salt and urea are dissolved in the deionized water, stir, add monomer and linking agent again, be made into mixing solutions, and place and stir the initiator that the back adds gelation on the agitator, polymerization reaction take place forms macromolecule network wet gel body in 35-75 ℃ of temperature range then, it is heated in 80-120 ℃ of saturated steam, urea generation hydrolysis, form precipitation with the metal ion in the network microcell, last, according to the difference of final generation product, the wet gel of gained is directly calcined, making particle diameter is 10~100 nanometers, epigranular, size-controllable spherical metal oxide and composite metal oxide powder;
Described soluble metallic salt is meant to generate sedimentary soluble metal nitrate or vitriol with the hydrolysate of urea that its consumption calculates by the content of each metal ion species in the desired final product; Urea is as the precipitation agent of microcell precipitin reaction, and its consumption is 1.2~3 times of mole numbers pressing the effective metal total ion concentration of reaction ratio calculating; Monomer is selected acrylamide for use, and linking agent is selected N for use, and N '-methylene-bisacrylamide, both consumptions are 10: 1~3: 1 by weight; The initiator of gelation is selected ammonium persulphate for use, and its adding proportion is 10~20wt% ammonium persulfate solution that every 100ml mixing solutions drips 2~1ml.
2, the preparation method of a kind of nano-metal-oxide according to claim 1 and complex metal oxides, it is characterized in that described mixing solutions adopts soluble metallic salt and urea with one or more to be dissolved in and to contain acrylamide monomer and N, formulated in the aqueous solution of N '-methylene-bisacrylamide.
3, the preparation method of a kind of nano-metal-oxide according to claim 1 and 2 and complex metal oxides, it is characterized in that described soluble metallic salt employing can generate sedimentary soluble metal nitrate with the hydrolysate of urea, it forms corresponding ammonium nitrate by product when forming precipitation by metallic ion in the microcell precipitation process.
4, the preparation method of a kind of nano-metal-oxide according to claim 1 and 2 and complex metal oxides, it is characterized in that described heat treated concrete calcining temperature and time needs decide according to the final product that generates, thermal treatment is residual byproduct of reaction C and the N of elimination when obtaining required nano-powder.
5, the preparation method of a kind of nano-metal-oxide according to claim 1 and 2 and complex metal oxides, it is characterized in that described various raw material, comprise soluble metal nitrate, urea, acrylamide monomer, N, N '-methylene-bisacrylamide, ammonium persulphate, its purity is more than the chemical pure.
CNB2005101266253A 2005-12-02 2005-12-02 Preparation method of nanometer metal oxide and composite metal oxide Expired - Fee Related CN100368281C (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016141613A (en) * 2015-02-05 2016-08-08 国立大学法人広島大学 Production method of metal oxide nanoparticle
CN107285391A (en) * 2017-06-01 2017-10-24 苏州乔纳森新材料科技有限公司 A kind of preparation method of magnetic Nano material
CN107986630A (en) * 2017-11-30 2018-05-04 华南协同创新研究院 A kind of preparation method of nano-bioactive glass powder
CN111613453A (en) * 2020-05-29 2020-09-01 大连交通大学 Preparation method of porous nickel cobaltate/graphene nano composite electrode material

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1112338C (en) * 1998-05-28 2003-06-25 中国科学技术大学 Method for preparing composite metal oxide ceramic powder material by using organic polymerization auxiliary prosess
JP3328649B2 (en) * 2001-04-04 2002-09-30 住友精化株式会社 Method for producing salt-resistant water-absorbent resin
CN1296284C (en) * 2004-08-09 2007-01-24 武汉大学 Process for preparing nano metal oxide material

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016141613A (en) * 2015-02-05 2016-08-08 国立大学法人広島大学 Production method of metal oxide nanoparticle
CN107285391A (en) * 2017-06-01 2017-10-24 苏州乔纳森新材料科技有限公司 A kind of preparation method of magnetic Nano material
CN107986630A (en) * 2017-11-30 2018-05-04 华南协同创新研究院 A kind of preparation method of nano-bioactive glass powder
CN111613453A (en) * 2020-05-29 2020-09-01 大连交通大学 Preparation method of porous nickel cobaltate/graphene nano composite electrode material
CN111613453B (en) * 2020-05-29 2022-02-08 大连交通大学 Preparation method of porous nickel cobaltate/graphene nano composite electrode material

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