CN108689423A - Monoclinic phase SmCO3(OH) preparation method of multilevel hierarchy crystallite - Google Patents

Monoclinic phase SmCO3(OH) preparation method of multilevel hierarchy crystallite Download PDF

Info

Publication number
CN108689423A
CN108689423A CN201811020458.8A CN201811020458A CN108689423A CN 108689423 A CN108689423 A CN 108689423A CN 201811020458 A CN201811020458 A CN 201811020458A CN 108689423 A CN108689423 A CN 108689423A
Authority
CN
China
Prior art keywords
crystallite
smco
multilevel hierarchy
preparation
monoclinic phase
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
CN201811020458.8A
Other languages
Chinese (zh)
Other versions
CN108689423B (en
Inventor
李凯斌
王书民
李盼
周春生
任有良
王丹
徐文文
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.)
Shangluo University
Original Assignee
Shangluo 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 Shangluo University filed Critical Shangluo University
Priority to CN201811020458.8A priority Critical patent/CN108689423B/en
Publication of CN108689423A publication Critical patent/CN108689423A/en
Application granted granted Critical
Publication of CN108689423B publication Critical patent/CN108689423B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F17/00Compounds of rare earth metals
    • C01F17/20Compounds containing only rare earth metals as the metal element
    • C01F17/247Carbonates
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/70Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • C01P2002/72Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/01Particle morphology depicted by an image
    • C01P2004/03Particle morphology depicted by an image obtained by SEM
    • 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
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/20Particle morphology extending in two dimensions, e.g. plate-like
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/50Agglomerated particles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

The invention discloses a kind of monoclinic phase SmCO3(OH) first Sm (NO are added under agitation in hexa by the preparation method of multilevel hierarchy crystallite3)3In solution, wherein Sm (NO3)3Molar ratio with hexa is(2:1)~(1:2);Reaction precursor liquid is placed under the conditions of 160 ~ 200 DEG C of microwave hydrothermals and reacts 15 ~ 60min, generates precipitation, after reaction cooled to room temperature;It isolates precipitation and washs drying, obtain SmCO3(OH) multilevel hierarchy crystallite.The present invention is with Sm (NO3)3For samarium source, multilevel hierarchy SmCO is realized under the conditions of microwave hydrothermal3(OH) successful structure;Short using the reaction time of microwave-hydrothermal method, instrument and equipment is simple, easy to operate, is easy to control;Obtained SmCO3(OH) purity of crystallite is high, crystallinity is strong, good dispersion.

Description

Monoclinic phase SmCO3(OH) preparation method of multilevel hierarchy crystallite
Technical field
The invention belongs to micro/nano material technical fields, more particularly to a kind of monoclinic phase SmCO3(OH) multilevel hierarchy is micro- Brilliant preparation method.
Background technology
Rare earth element has 4fx5d0-16s2Electronic structure, because its atomic radius is big and easily lose outer layer 6s, 5d or 4f electronics, and there is very strong activity so that rare earth metal and its compound show typical light, electricity, magnetic and catalysis spy Property.Specific micro-/ nano manufacturing technology is introduced into the preparation process of functional rareearth material, make the advantage of rare earth material with The characteristic of micro/nano material is combined, and obtained micro-/ nano rare earth material is in rare earth permanent-magnetic material, hydrogen storage material, catalysis material The application of material, micro-/ nano rare earth phosphor and varistor etc. is not only expected to realize the upgrading of conventional industries, but also Will promote the advantage that the added value of rare earth material utilizes and further plays China's rare earth resources has important research valence Value and meaning.The rare earth metal subcarbonate of different-shape, such as fusiform CeOHCO3 [Zhao D L, Yang Q, Han Z H, et al. Biomolecule-assisted Synthesis of Rare Earth Hydroxycarbonates [J]. Solid State Sciences, 2008, 10: 31-39.], dodecahedron shape NdOHCO3 [Xu Z Y, Zhang Y J, Fang Z Y, et al. Controllable Synthesis and Optical Properties of NdOHCO3 Dodecahedral Microcrystals [J]. Materials Research Bulletin, 2010, 45: 74-79.]And dumbbell shaped PrOHCO3 [Zhao D L, Yang Q, Han Z H, et al. Rare Earth Hydroxycarbonate Materials with Hierarchical Structures: Preparation and Characterization, and Catalytic Activity of Derived Oxides [J]. Solid State Sciences, 2008, 10: 1028-103.]Etc. existing document report.
Pattern, size, crystal form and the exposure crystal face of inorganic semiconductor material have weight for its light, electricity, magnetic and chemical characteristic The influence wanted.Basic carbonate samarium is widely used in electronics and ceramic industry as a kind of important lanthanide rare compound-material Field.Because samarium is easily magnetized and is not easy demagnetization, basic carbonate samarium is expected to have in solid state electronic device and superconductor important Application.It is also widely used in the preparation of samarium oxide using basic carbonate samarium as presoma.In addition, some researches show that Eu3+It mixes Miscellaneous SmCO3(OH) it can be used for preparing optical conversion film to improve the utilization rate of light.Such as, octahedral shape SmCO3(OH) [Zhang Y J, He H M, Yang X Z, et al. Morphology-controlled Synthesis, Characterization, Growth Mechanism of SmCO3(OH) with High Uniform Size and Photoluminescence Property of SmCO3(OH): Eu3+ [J]. Powder Technology, 2012, 224: 175-182.]And diamond shape SmCO3(OH) [Yin X B, Zhang Y J, Fang Z Y, et al. Hydrothermal Synthesis of Rhombus-like SmCO3OH Microplates and Its Photoluminescence Property Doped with Eu3+ [J]. Chinese Journal of Chemical Physics, 2010, 23: 102-106.].Currently reported SmCO3(OH) preparation method mostly uses hydro-thermal method, system The standby period is long, and energy consumption is more, the SmCO prepared by conventional hydrothermal method3(OH) it is mostly two-dimensional structure(Such as diamond shape), the utilization to photon Rate is relatively low, needs doping with rare-earth ions such as Eu3+To improve its optical property.
Invention content
The purpose of the present invention is to provide a kind of monoclinic phase SmCO3(OH) preparation method of multilevel hierarchy crystallite, solves SmCO in the prior art3(OH) it is more than diamond structure and long preparation period, energy consumption and the problem low to photon utilization rate.
The technical solution adopted in the present invention is monoclinic phase SmCO3(OH) preparation method of multilevel hierarchy crystallite, is specifically pressed It is carried out according to following steps:
Under agitation Sm (NO are added in hexa by step 13)3In solution, continue to stir 10min and formed to react Precursor liquid;
Reaction precursor liquid is placed in microwave hydrothermal liner and reacts by step 2, generates precipitation, naturally cools to room after reaction Temperature;
Step 3 isolates the precipitation in step 2 and washs drying, obtains the flower-like structure SmCO that strip is self-assembled into3(OH) micro- It is brilliant.
Further, Sm (NO in the step 13)3A concentration of 0.2 ~ 0.5molL of solution-1, the pH of reaction precursor liquid =8~9。
Further, wherein Sm (NO in the step 13)3Molar ratio with hexa is(2:1)~(1:2).
Further, packing ratio of the reaction precursor liquid in microwave hydrothermal liner is 50% in the step 2.
Further, in the step 2 under the conditions of 160 ~ 200 DEG C of microwave hydrothermals react 15 ~ 60min, reaction temperature and Reaction time is determined according to the property and reaction condition of reactant, and the higher the reaction time of temperature is relatively short, temperature compared with Low the reaction time is appropriately extended, and full grown crystal can be obtained with this.
Further, the drying in the step 3 is dry 2 ~ 4h in 60 ~ 80 DEG C of electric vacunm drying case, dry Too high or too low for temperature and drying time is long or too short, cannot fully dry and non-caking powder.
The invention has the advantages that the present invention is with Sm (NO3)3For samarium source, not only as alkali source but also made using hexa For template, multilevel hierarchy SmCO is carried out using microwave-hydrothermal method3(OH) preparation of crystallite.Obtained SmCO3(OH) crystallite Purity is higher, and good crystallinity, oriented growth is apparent, and the flower-shaped multilevel hierarchy that strip is self-assembled into is presented, and flower-shaped multilevel hierarchy removes Be conducive to outside the conduction of electronics, the absorbability of light is also promoted.SmCO is prepared relative to traditional hydro-thermal method3(OH), The structure of product prepared by the present invention is 3D structures, and 3D structures are by one or more basic in zero dimension, one-dimensional and two dimension The composite material of structural unit composition, the 3D structures of same material are compared with other dimensions, because 3D structures have gathered other simultaneously The advantage of dimension can show more excellent photoelectric characteristic;And preparation process is completed in a relatively short time.The reaction is with water As reaction dissolvent, safety is good, and feasibility is strong, easy to operate, very economical, practical, has good industrial prospect.This The flower-shaped multilevel hierarchy that invention strip obtained is self-assembled into is conducive to the conduction of electronics so that SmCO3(OH) in solid-state electronic It has great application prospect in component and superconductor.
Description of the drawings
In order to more clearly explain the embodiment of the invention or the technical proposal in the existing technology, to embodiment or will show below There is attached drawing needed in technology description to be briefly described, it should be apparent that, the accompanying drawings in the following description is only this Some embodiments of invention for those of ordinary skill in the art without creative efforts, can be with Obtain other attached drawings according to these attached drawings.
Fig. 1 is the SmCO prepared by the present invention3(OH) X-ray diffraction of crystallite(XRD)Figure.
Fig. 2 is the SmCO prepared by the present invention3(OH) scanning electron microscope of crystallite(SEM)Figure.
Specific implementation mode
Below in conjunction with the embodiment of the present invention, technical scheme in the embodiment of the invention is clearly and completely described, Obviously, described embodiments are only a part of the embodiments of the present invention, instead of all the embodiments.Based in the present invention Embodiment, every other embodiment obtained by those of ordinary skill in the art without making creative efforts, all Belong to the scope of protection of the invention.
Embodiment 1:
Step 1 will analyze pure Sm (NO3)3·6H2O, which is dissolved in 50mL distilled water, is made Sm3+A concentration of 0.5molL-1It is molten Liquid;
Step 2 will analyze pure hexa addition 0.5molL under magnetic stirring-1 Sm(NO3)3In solution so that Sm3+Molar ratio with hexa is 2:1, continue to be added in 100mL microwave hydrothermals reaction liner after stirring 10min;It will Reaction precursor liquid is placed in microwave hydrothermal instrument, is warming up to 170 DEG C of reaction 30min, after reaction cooled to room temperature;
Step 3, product utilize distilled water and absolute ethyl alcohol centrifuge washing 4 times successively, are placed in 60 DEG C of electric vacunm drying case Dry 4 h, that is, obtain the bouquet that irregular sheet is self-assembled into, tightly packed between piece, and the size of bouquet is inhomogenous.
Embodiment 2:
Step 1 will analyze pure Sm (NO3)3·6H2O, which is dissolved in 50mL distilled water, is made Sm3+A concentration of 0.25molL-1It is molten Liquid;
Step 2 will analyze pure hexa addition 0.25molL under magnetic stirring-1 Sm(NO3)3In solution so that Sm3+Molar ratio with hexa is 1:1, continue to be added in 100mL microwave hydrothermals reaction liner after stirring 10min;It will Reaction precursor liquid is placed in microwave hydrothermal instrument, is warming up to 170 DEG C of reaction 45min, after reaction cooled to room temperature;
Step 3, product utilize distilled water and absolute ethyl alcohol centrifuge washing 5 times successively, are placed in 70 DEG C of electric vacunm drying case Dry 3 h obtain the flower-shaped multilevel hierarchy that strip is self-assembled into, and good dispersion, size uniformity.
Embodiment 3:
Step 1 will analyze pure Sm (NO3)3·6H2O, which is dissolved in 50mL distilled water, is made Sm3+A concentration of 0.4molL-1It is molten Liquid;
Step 2 will analyze pure hexa addition 0.4molL under magnetic stirring-1 Sm(NO3)3In solution so that Sm3+Molar ratio with hexa is 1.5:1, continue to be added in 100mL microwave hydrothermals reaction liner after stirring 10min; Reaction precursor liquid is placed in microwave hydrothermal instrument, is warming up to 200 DEG C of reaction 15min, after reaction cooled to room temperature;
Step 3, product utilize distilled water and absolute ethyl alcohol centrifuge washing 6 times successively, are placed in 80 DEG C of electric vacunm drying case Dry 2 h, that is, obtain the bouquet that irregular sheet is self-assembled into, tightly packed between piece, and the size of bouquet is inhomogenous.
Embodiment 4:
Step 1 will analyze pure Sm (NO3)3·6H2O, which is dissolved in 50mL distilled water, is made Sm3+A concentration of 0.35molL-1It is molten Liquid;
Step 2 will analyze pure hexa addition 0.35molL under magnetic stirring-1 Sm(NO3)3In solution so that Sm3+Molar ratio with hexa is 1:1.5, continue to be added in 100mL microwave hydrothermals reaction liner after stirring 10min; Reaction precursor liquid is placed in microwave hydrothermal instrument, is warming up to 180 DEG C of reaction 30min, after reaction cooled to room temperature;
Step 3, product utilize distilled water and absolute ethyl alcohol centrifuge washing 4 times successively, are placed in 80 DEG C of electric vacunm drying case Dry 2 h obtain the product of the mixing pattern of strip and flower-like structure.
Embodiment 5:
Step 1 will analyze pure Sm (NO3)3·6H2O, which is dissolved in 50mL distilled water, is made Sm3+A concentration of 0.2molL-1It is molten Liquid;
Step 2 will analyze pure hexa addition 0.2molL under magnetic stirring-1 Sm(NO3)3In solution so that Sm3+Molar ratio with hexa is 1:2, continue to be added in 100mL microwave hydrothermals reaction liner after stirring 10min;It will Reaction precursor liquid is placed in microwave hydrothermal instrument, is warming up to 160 DEG C of reaction 60min, after reaction cooled to room temperature;
Step 3, product utilize distilled water and absolute ethyl alcohol centrifuge washing 4 times successively, are placed in 60 DEG C of electric vacunm drying case Dry 4 h, that is, obtain the non-uniform random plate cross structure of size.
Sm in embodiment 23+Proportioning with the amount of hexa substance is 1:1, six methylenes in reaction system at this time Hydrolysis is changed into OH to urotropine mostly-And CO3 2-, with the Sm to dissociate in solution3+In conjunction with being formed by monoclinic phase SmCO3(OH) brilliant Core grows into elongate configuration in the two-dimensional direction, and three-dimensional flower-shaped knot is self-assembled under the action of intermolecular hydrogen bonding and Van der Waals force Structure and good dispersion, size are more uniform.
Fig. 1 is the SmCO prepared by the embodiment of the present invention 23(OH) XRD diagram of crystallite can obtain the product of preparation No. JCPDS is 41-0663, as SmCO3(OH), from which further follow that the purity of product is high, crystallinity is strong, crystal structure is monocline Phase, orientation growth are apparent.
Fig. 2 is the SmCO prepared by the embodiment of the present invention 23(OH) scanned photograph that crystallite is shot when amplifying 10,000 times, Product is the flower-like structure that strip is self-assembled into, good dispersion as seen from the figure.
For the present invention using hexa not only as alkali source but also as template, hexa is a kind of weak organic Alkali, when temperature be higher than 150 DEG C, NH can be decomposed into through hydrolytic process4 +,OH-And CO3 2-, and there are four mutually for hexa tool The structure feature of condensed Trianacyclohexane ring, is easily complexed with metal ion in liquid phase reaction course, and to product Nucleation and crystalline growth process play certain regulating and controlling effect.
Many experiments find that the pattern of suitable samarium ion concentrations on product has a certain impact, when samarium ion concentration mistake It cannot get three-dimensional multistage structure when small and excessive;The increase of hexa addition makes OH in reaction system-With CO3 2-Concentration increase, the nucleation amount of product increases, and a large amount of nucleus is in the state for growth of vying each other;In addition, reactant The presence of excessive hexa in system, can also be adsorbed on certain crystal faces of crystal grain, it is suppressed that difference is intercrystalline certainly Assembling process, and finally obtained part strip and the mixing pattern of flower-like structure and the production of random plate cross structure Object;As the addition for reducing hexa in reaction system, excessive Sm3+It is adsorbed on grain surface, is influenced in two-dimensional directional Reach full growth, obtained more particle and the mixing pattern of flower-shaped multilevel hierarchy that strip is self-assembled into.When reaction precursor liquid PH=8 ~ 9, product can be generated, adjust the addition of hexa, be to regulate and control to product morphology.It replaces Alkali source will be unable to obtain the multilevel hierarchy of the present invention, and when using sodium carbonate and urea for alkali source, product is octahedral structure.
The present invention provides a kind of microwave-hydrothermal methods being simple and efficient to prepare multilevel hierarchy SmCO3(OH) method of crystallite. The reaction time of microwave-hydrothermal method is short, and instrument and equipment is simple, easy to operate, is easy to control;The present invention chooses hexa Not only it had been used as alkali source but also had been used as template, and realized multilevel hierarchy SmCO under specified conditions3(OH) controlledly synthesis of crystallite.
Each embodiment in this specification is all made of relevant mode and describes, identical similar portion between each embodiment Point just to refer each other, and each embodiment focuses on the differences from other embodiments.Especially for system reality For applying example, since it is substantially similar to the method embodiment, so description is fairly simple, related place is referring to embodiment of the method Part explanation.
The foregoing is merely illustrative of the preferred embodiments of the present invention, is not intended to limit the scope of the present invention.It is all Any modification, equivalent replacement, improvement and so within the spirit and principles in the present invention, are all contained in protection scope of the present invention It is interior.

Claims (6)

1. monoclinic phase SmCO3(OH) preparation method of multilevel hierarchy crystallite, which is characterized in that specifically follow the steps below:
Under agitation Sm (NO are added in hexa by step 13)3In solution, continue before stirring 10min formation reactions Drive liquid;
Reaction precursor liquid is placed in microwave hydrothermal liner and reacts by step 2, generates precipitation, naturally cools to room after reaction Temperature;
Step 3 isolates the precipitation in step 2 and washs drying, obtains the flower-like structure SmCO that strip is self-assembled into3(OH) micro- It is brilliant.
2. monoclinic phase SmCO according to claim 13(OH) preparation method of multilevel hierarchy crystallite, which is characterized in that described Sm (NO in step 13)3A concentration of 0.2 ~ 0.5molL of solution-1, pH=8 ~ 9 of reaction precursor liquid.
3. monoclinic phase SmCO according to claim 13(OH) preparation method of multilevel hierarchy crystallite, which is characterized in that described Wherein Sm (NO in step 13)3Molar ratio with hexa is(2:1)~(1:2).
4. monoclinic phase SmCO according to claim 13(OH) preparation method of multilevel hierarchy crystallite, which is characterized in that described Packing ratio of the reaction precursor liquid in microwave hydrothermal liner is 50% in step 2.
5. monoclinic phase SmCO according to claim 13(OH) preparation method of multilevel hierarchy crystallite, which is characterized in that described 15 ~ 60min is reacted in step 2 under the conditions of 160 ~ 200 DEG C of microwave hydrothermals.
6. monoclinic phase SmCO according to claim 13(OH) preparation method of multilevel hierarchy crystallite, which is characterized in that described Drying in step 3 is dry 2 ~ 4h in 60 ~ 80 DEG C of electric vacunm drying case.
CN201811020458.8A 2018-09-03 2018-09-03 Monoclinic phase SmCO3(OH) preparation method of multilevel structure crystallite Active CN108689423B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811020458.8A CN108689423B (en) 2018-09-03 2018-09-03 Monoclinic phase SmCO3(OH) preparation method of multilevel structure crystallite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811020458.8A CN108689423B (en) 2018-09-03 2018-09-03 Monoclinic phase SmCO3(OH) preparation method of multilevel structure crystallite

Publications (2)

Publication Number Publication Date
CN108689423A true CN108689423A (en) 2018-10-23
CN108689423B CN108689423B (en) 2019-10-18

Family

ID=63841457

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811020458.8A Active CN108689423B (en) 2018-09-03 2018-09-03 Monoclinic phase SmCO3(OH) preparation method of multilevel structure crystallite

Country Status (1)

Country Link
CN (1) CN108689423B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112875741A (en) * 2021-01-28 2021-06-01 浙江师范大学 Broadband hydrated cerium oxycarbonate microwave absorbent, and preparation process and application thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105032392A (en) * 2015-07-27 2015-11-11 陕西科技大学 Method for preparing SmCO3 (OH)/ZnO nanocomposite by homogeneous hydrothermal method

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105032392A (en) * 2015-07-27 2015-11-11 陕西科技大学 Method for preparing SmCO3 (OH)/ZnO nanocomposite by homogeneous hydrothermal method

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
HANSONG XUE ET AL.: ""Microwave-Assisted Hydrothermal Synthesis of Sm2O3 Nanoparticles and their Optical Properties"", 《JOURNAL OF NANO RESEARCH》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112875741A (en) * 2021-01-28 2021-06-01 浙江师范大学 Broadband hydrated cerium oxycarbonate microwave absorbent, and preparation process and application thereof

Also Published As

Publication number Publication date
CN108689423B (en) 2019-10-18

Similar Documents

Publication Publication Date Title
Xu et al. Preparation of highly dispersed YAG nano-sized powder by co-precipitation method
Wang et al. Chemical co-precipitation synthesis and properties of pure-phase BiFeO3
CN102745675A (en) Preparation method of spinel-type magnetic MFe2O4/graphene composite material
CN103523824B (en) The preparation method of nano-sheet ferroelectric material for a kind of photocatalysis
CN108083316A (en) A kind of preparation method of nano rareearth oxidate powder body
CN105271405A (en) Material based on bismuth oxycarbonate or bismuth oxide nano tube and preparation method thereof
CN104528799A (en) Preparation method of ultrafine magnesium-based rare earth hexaaluminate powder
Qian et al. Control of the morphology and composition of yttrium fluoride via a salt-assisted hydrothermal method
CN103833080B (en) A kind of preparation method of molybdic acid cadmium porous ball
CN108689423B (en) Monoclinic phase SmCO3(OH) preparation method of multilevel structure crystallite
CN101759162B (en) Low-temperature liquid phase synthesizing method of monodisperse square crystalline phase ferrous selenide square nanometer sheet
CN103131417A (en) Eu doped YPO4 microballoon and preparation method thereof
CN105152192B (en) A kind of preparation method of magnesia/rare earth oxide core shell structure flower-like nanometer composite
CN105314672A (en) Method for preparing cobalt-doped zinc oxide nanorods through sol-gel
CN109879305B (en) Preparation of micron-sized monodisperse LaAlO3:xMm+Method for producing spherical particles
CN102320659B (en) Method for synthesizing lanthanum-vanadate nano material by adopting microwave-radiation method
CN105858707B (en) Preparing method for Sm2O3 nanocrystalline
CN103508492B (en) Method for rapidly preparing NdWO4(OH) nanopowder
CN106044831B (en) A kind of sluggish precipitation prepares sheet SmOHCO3Nanocrystalline method
CN105752957A (en) Method for preparing nano-scale rare-earth phosphate phosphor by self-sacrificing template method
CN101648726B (en) Hydrothermal synthesis method of LuO(OH) nanorods and Lu2O3 nanorods luminescent powder
CN103991907B (en) A kind of preparation method of manganous carbonate nanofiber ball
CN102464348A (en) Hydrothermal preparation method of lutetium oxide nanometer powder
CN108384544B (en) Tetragonal YPO4:Ln3+Spherical fluorescent particles and preparation method thereof
CN102001696A (en) Method for preparing magnesium-aluminum spinel nano particle powder

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