CN111634935A - Microwave preparation method of nano rare earth oxide - Google Patents
Microwave preparation method of nano rare earth oxide Download PDFInfo
- Publication number
- CN111634935A CN111634935A CN202010330543.5A CN202010330543A CN111634935A CN 111634935 A CN111634935 A CN 111634935A CN 202010330543 A CN202010330543 A CN 202010330543A CN 111634935 A CN111634935 A CN 111634935A
- Authority
- CN
- China
- Prior art keywords
- rare earth
- microwave
- earth oxide
- praseodymium
- neodymium
- 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.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F17/00—Compounds of rare earth metals
- C01F17/10—Preparation or treatment, e.g. separation or purification
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F17/00—Compounds of rare earth metals
- C01F17/20—Compounds containing only rare earth metals as the metal element
- C01F17/206—Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F17/00—Compounds of rare earth metals
- C01F17/20—Compounds containing only rare earth metals as the metal element
- C01F17/206—Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion
- C01F17/224—Oxides or hydroxides of lanthanides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F17/00—Compounds of rare earth metals
- C01F17/20—Compounds containing only rare earth metals as the metal element
- C01F17/206—Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion
- C01F17/241—Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion containing two or more rare earth metals, e.g. NdPrO3 or LaNdPrO3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
The invention discloses a microwave preparation method of nano rare earth oxide, which comprises the following steps of (1) surface treatment: taking rare earth salt solution to adjust the pH value to be alkaline, and adding a surface auxiliary agent to obtain rare earth-containing solution for surface treatment; (2) precipitation reaction: dropwise adding a precipitant into the rare earth-containing solution subjected to surface treatment while stirring, and aging, filtering and washing to obtain a corresponding rare earth precipitate; (3) microwave calcination: and placing the precipitate into a microwave reactor for microwave heating and calcining to obtain the nano rare earth oxide powder. The invention adopts a microwave heating calcination method and surface additives to prepare the nano rare earth oxide with uniform granularity, consistent appearance and good dispersibility.
Description
Technical Field
The invention relates to the field of rare earth, in particular to a microwave preparation method of a nanometer rare earth oxide.
Background
Praseodymium oxide (Pr)6O11) Is an inorganic compound, having the english name Praseodymium oxide, which can be used for glass, metallurgy, and as a phosphor additive, etc. Praseodymium oxide is one of the important products in light rare earth products. Because of its unique physical and chemical properties, it can be used in the fields of ceramics, glass, rare earth permanent magnet, rare earth cracking catalyst, rare earth polishing powder, grinding material and additive, etc., and is increasingly extensive and good in prospect. Since the 90 s, the praseodymium oxide production technology and equipment in China have been greatly improved and perfected, the product and the yield are increased rapidly, the praseodymium oxide can not only meet the requirements of domestic application amount and market, but also have a considerable amount of export. Therefore, the current production technology, product and yield of praseodymium oxide, the demand for domestic and foreign markets, and the like all belong to the same industry in the world. In the future, the praseodymium oxide industry in China can be expected to be developed more quickly. At present, rare earth resources in China still live at the top of the world, wherein the industrial reserve of praseodymium is about 210 ten thousand tons, which provides a full material basis for the continuous development of praseodymium industry in China in future and is also a unique advantage in China. Praseodymium oxide has a relatively high application prospect in the aspects of rare earth glass, rare earth ceramic, rare earth permanent magnet and the like, and also has a great number of applications in more aspects of corundum grinding wheels, polishing, petroleum catalytic cracking, steelmaking additives and the like.
Neodymium oxide is a rare earth oxide with wide application and is mainly applied to neodymium iron boron (Nd-Fe-B) permanent magnets, television glass shells, glass coloring, fluorescent materials, laser materials and rubber industrial additives, and because the neodymium oxide has elegant color tone and good color change effect, the neodymium oxide is also widely applied to high-tech fields such as ceramics, textile dyeing, superconduction and other functional materials, and the growth momentum is very strong. In recent years, research on the application of neodymium oxide in the field of catalysis is increasingly extensive, such as catalysis of polycarboxylic acid synthesis, fatty alcohol amination, rubber synthesis and the like, and particularly, nanometer neodymium oxide with large specific surface area has better properties and application and higher catalytic activity. The nano neodymium oxide with the concentration of 1.5-2.5% is added into the magnesium alloy or the aluminum alloy, so that the high-temperature performance, the air tightness and the corrosion resistance of the alloy can be improved, and the alloy can be widely used as aerospace materials. In addition, the nanometer yttrium oxide aluminum garnet doped with nanometer neodymium oxide generates short-wave laser beams, and is widely used for welding and cutting thin materials with the thickness of less than 10mm in industry. In medical treatment, the nanometer yttrium oxide aluminum garnet laser doped with nanometer neodymium oxide replaces a scalpel to be used for removing an operation or disinfecting a wound.
Pr-Nd, metal Pr-Nd, is a silver gray metal ingot. The total content of rare earth is more than 99 percent. The neodymium content in the metal is about 75 percent, and the praseodymium content is about 25 percent. The metal praseodymium neodymium is easy to oxidize in the air, belongs to low-toxicity material, and has the toxicity equivalent to that of iron. The rare earth element is hardly absorbed because it is almost completely hydrolyzed in the animal body to form a hydroxide colloid and precipitate. Can be stored in dry environment for a long time. The praseodymium-neodymium alloy is a main raw material for producing high-performance neodymium-iron-boron permanent magnet materials. The percentage of the neodymium iron boron permanent magnet material in the cost of the neodymium iron boron permanent magnet material is about 27%. The praseodymium-neodymium oxide is used for deep processing and for glass, ceramics, magnetic materials and the like. The Dy-Fe alloy is mainly used for making Nd-Fe-B permanent-magnet material, giant magnetostrictive alloy, magneto-optical recording material and nuclear fuel diluent.
At present, a precipitation method, an extraction separation method and an ion exchange method are mostly adopted in the method for preparing the nanometer rare earth oxide (praseodymium oxide or neodymium oxide or praseodymium neodymium oxide), wherein the precipitation method cannot be applied to industrial production due to low rare earth recovery rate, small yield and high cost, and the prepared praseodymium oxide (or neodymium oxide or praseodymium neodymium oxide) has larger granularity and different shapes and is uncontrollable in the heating process due to nonuniform agglomeration caused by internal and external heating of particles during high-temperature reaction of the precipitation method; the extraction separation method has wide application in industrial production, but has the defects of complex process and high consumption cost of an extracting agent; the ion exchange method has the defects of long preparation process, troublesome operation, low rare earth recovery rate, low product purity and yield and the like.
Disclosure of Invention
In order to solve the technical problems, the invention provides a method for preparing a nano rare earth oxide (praseodymium oxide, neodymium oxide or praseodymium neodymium oxide) by adopting a precipitation method and a microwave heating calcination method, and the method ensures that the prepared nano rare earth oxide has uniform granularity and good dispersibility.
The purpose of the invention is realized by the following technical scheme:
a microwave preparation method of nanometer rare earth oxide comprises the following steps,
(1) surface treatment: taking rare earth salt solution to adjust the pH value to be alkaline, and adding a surface auxiliary agent to obtain rare earth-containing solution for surface treatment;
(2) precipitation reaction: dropwise adding a precipitant into the rare earth-containing solution subjected to surface treatment while stirring, and aging, filtering and washing to obtain a rare earth precipitate;
(3) microwave calcination: and placing the rare earth precipitate into a microwave reactor for microwave heating and calcining to obtain the nano rare earth oxide powder.
Preferably, the rare earth salt solution is praseodymium salt, neodymium salt or praseodymium-neodymium salt; the concentration of the rare earth salt solution is 0.1-2 mol/L.
Preferably, in the step (1), the surface auxiliary agent is one of stearic acid, polyacrylamide, citric acid and sodium dodecyl sulfate.
Preferably, the addition amount of the surface auxiliary agent is 5-15% of the molar mass of the rare earth salt solution.
Preferably, the precipitant in step (2) is any one or a combination of oxalic acid, carbonic acid, ammonium bicarbonate, oxalate and carbonate, and when the precipitant is a combined precipitant, the ratio of oxalate: carbonate 1:0.2-1.8 or oxalate: carbonate radical: bicarbonate radical 0.8-1.5: 0.5-2: 0.1-0.5.
Preferably, the addition amount of the precipitant is in a molar ratio of precipitant: rare earth is added in a ratio of 1-3: 1.
Preferably, the precipitant is added at a rate of 0.5-3L/min.
Preferably, the frequency of the microwave heating calcination in the step (3) is 915 +/-50 MHz or 2450 +/-50 MHz, and the power is 1-10 kw.
Preferably, the microwave heating calcination temperature is 800-1200 ℃, and the calcination time is 2-6 h.
Preferably, the microwave output means includes one or a combination of a continuous wave and a pulse wave.
The invention has the following beneficial effects:
1. in the preparation process, the surface auxiliary agent is added, a layer of diaphragm is generated on the surface of the generated crystal grain, the surface energy of the diaphragm is reduced, the crystal grain is prevented from growing in the precipitation process, and the agglomeration of the crystal grain is prevented; the nano powder particles prepared by the aid are finer and more uniform in size.
2. The adding speed of the precipitant is controlled, so that the precipitant is more uniform, the formed precipitant is dispersed in the solution and is covered with the surface auxiliary agent in a complexing manner, meanwhile, the combined precipitant can achieve a better precipitation effect, a coprecipitate is formed, and the dispersibility of the precipitant is better.
3. The invention adopts the microwave heating technology, the surface and the inside of the crystal grains are simultaneously heated in the heating and calcining process, the heating is rapid, the heat conduction is uniform, the resonance is generated in the material to generate heat through the oscillation of the specific microwave frequency, the heating rate and the time are controllable, the decomposed gas is rapidly expanded after the surface auxiliary agent and the oxalic acid/carbonic acid reach the decomposition or combustion temperature, a certain explosion effect is realized, and the prepared product is more delicate, the specific surface area is higher, the granularity is uniform, and the shape of the nano rare earth oxide is consistent.
4. The microwave heating method has the advantages that the heating process is controllable, the heating efficiency is high, the defect of high energy consumption in the traditional preparation method can be effectively reduced, and the microwave heating method has important application prospects.
Detailed Description
In order to make those skilled in the art better understand the technical solutions in the present application, the following will clearly and completely describe the technical solutions in the present application with reference to the embodiments, and it is obvious that the described embodiments are only a part of the embodiments of the present application, and all other embodiments obtained by a person of ordinary skill in the art without making creative efforts based on the embodiments in the present application shall fall within the protection scope of the present application.
Example 1
A microwave preparation method of nanometer praseodymium oxide comprises the following steps,
(1) surface treatment: adjusting the pH value of a praseodymium salt solution with the concentration of 0.1mol/L to be alkaline, and adding stearic acid with the molar mass of 5% of the praseodymium salt solution to obtain a praseodymium-containing solution for surface treatment;
(2) precipitation reaction: adding oxalic acid dropwise into the praseodymium-containing solution subjected to surface treatment at the speed of 0.5L/min while stirring, and aging, filtering and washing to obtain praseodymium-containing precipitate; the oxalic acid: praseodymium is added according to a molar ratio of 1: 1;
(3) microwave calcination: putting the praseodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 1h at the frequency of 915 +/-50 MHz, the power of 1kw and the temperature of 800 ℃ to obtain nano praseodymium oxide powder; the microwave output mode is a continuous wave mode.
Example 2
A microwave preparation method of nanometer neodymium oxide comprises the following steps,
(1) surface treatment: adjusting the pH value of a neodymium salt solution with the concentration of 2mol/L to be alkaline, and adding polyacrylamide with the molar mass of 15% of the neodymium salt solution to obtain a neodymium-containing solution with surface treatment; the rare earth salt solution is;
(2) precipitation reaction: dropwise adding ammonium bicarbonate into the neodymium-containing solution subjected to surface treatment at the speed of 3L/min while stirring, and aging, filtering and washing to obtain a neodymium-containing precipitate; the ammonium bicarbonate: the molar ratio of neodymium is 3: 1;
(3) microwave calcination: putting the neodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 5h at the frequency of 2450 +/-50 MHz, the power of 10kw and the temperature of 1200 ℃ to obtain nano neodymium oxide powder; the microwave output mode is a pulse wave mode.
Example 3
A microwave preparation method of nanometer praseodymium neodymium oxide comprises the following steps,
(1) surface treatment: taking a praseodymium-neodymium salt solution with the concentration of 0.5mol/L to adjust the pH value to be alkaline, and adding citric acid with the molar mass of 10% of the praseodymium-neodymium salt solution to obtain a praseodymium-neodymium containing solution with surface treatment;
(2) precipitation reaction: dropwise adding a precipitator into the praseodymium-neodymium-containing solution subjected to surface treatment at the speed of 1.5L/min while stirring, and aging, filtering and washing to obtain a praseodymium-neodymium-containing precipitate; the precipitant is oxalate: carbonate 1: 0.2; the precipitating agent is: praseodymium and neodymium are mixed according to the molar ratio of 2: 1;
(3) microwave calcination: placing the praseodymium-neodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 2h at the frequency of 2450 +/-50 MHz, the power of 8kw and the temperature of 1000 ℃ to obtain nanometer praseodymium-neodymium oxide powder; the microwave output mode comprises a continuous wave mode and a pulse wave mode.
Example 4
A microwave preparation method of nanometer praseodymium oxide comprises the following steps,
(1) surface treatment: adjusting the pH value of a praseodymium salt solution with the concentration of 0.9mol/L to be alkaline, and adding sodium dodecyl sulfate with the molar mass of 12% of the praseodymium salt solution to obtain a praseodymium-containing solution for surface treatment;
(2) precipitation reaction: dripping a precipitator into the praseodymium-containing solution subjected to surface treatment at the speed of 2.7L/min while stirring, and aging, filtering and washing to obtain praseodymium-containing precipitate; the precipitant is oxalate: carbonate radical: bicarbonate radical 0.8: 2: 0.5; the precipitating agent is: praseodymium is added according to the molar ratio of 2.5: 1;
(3) microwave calcination: putting the praseodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 4 hours at the frequency of 2450 +/-50 MHz, the power of 3kw and the temperature of 900 ℃ to obtain nanometer praseodymium oxide powder; the microwave output mode comprises a mode of combining continuous waves and pulse waves.
Example 5
A microwave preparation method of nanometer neodymium oxide comprises the following steps,
(1) surface treatment: adjusting the pH value of a neodymium salt solution with the concentration of 1.5mol/L to be alkaline, and adding polyacrylamide with the molar mass of 8% of the neodymium salt solution to obtain a neodymium-containing solution with surface treatment;
(2) precipitation reaction: dropwise adding a precipitator into the neodymium-containing solution subjected to surface treatment at the speed of 1.8L/min while stirring, and aging, filtering and washing to obtain a neodymium-containing precipitate; the precipitant is oxalate: carbonate 1: 1.8; the precipitating agent is: neodymium in a molar ratio of 1.5: 1;
(3) microwave calcination: putting the neodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 3h at the frequency of 915 +/-50 MHz, the power of 4kw and the temperature of 1100 ℃ to obtain nano neodymium oxide powder; the microwave output mode comprises a continuous wave mode and a pulse wave mode.
Example 6
A microwave preparation method of nanometer praseodymium neodymium oxide comprises the following steps,
(1) surface treatment: taking a praseodymium-neodymium salt solution with the concentration of 1.5mol/L to adjust the pH value to be alkaline, and adding polyacrylamide with the molar mass of 8% of the praseodymium-neodymium salt solution to obtain a praseodymium-neodymium containing solution with surface treatment;
(2) precipitation reaction: dropwise adding a precipitator into the praseodymium-neodymium-containing solution subjected to surface treatment at the speed of 2.6L/min while stirring, and aging, filtering and washing to obtain a praseodymium-neodymium-containing precipitate; the precipitant is oxalate: carbonate 1: 1.2; the precipitating agent is: praseodymium and neodymium are expressed in a molar ratio of 2.2: 1;
(3) microwave calcination: placing the praseodymium-neodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 3h at the frequency of 915 +/-50 MHz, the power of 4kw and the temperature of 1100 ℃ to obtain nanometer praseodymium-neodymium oxide powder; the microwave output mode comprises a continuous wave mode and a pulse wave mode.
Example 7
A microwave preparation method of nanometer praseodymium oxide comprises the following steps,
(1) surface treatment: adjusting the pH value of a praseodymium salt solution with the concentration of 1.5mol/L to be alkaline, and adding polyacrylamide with the molar mass of 8% of the praseodymium salt solution to obtain a praseodymium-containing solution for surface treatment;
(2) precipitation reaction: dripping a precipitator into the praseodymium-containing solution subjected to surface treatment at the speed of 2.7L/min while stirring, and aging, filtering and washing to obtain praseodymium-containing precipitate; the precipitant is oxalate: carbonate radical: bicarbonate radical 1.5: 0.5: 0.1; the precipitating agent is: praseodymium is added according to the molar ratio of 2.1: 1;
(3) microwave calcination: putting the praseodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 3h at the frequency of 915 +/-50 MHz, the power of 4kw and the temperature of 1100 ℃ to obtain nano praseodymium oxide powder; the microwave output mode comprises a continuous wave mode and a pulse wave mode.
Example 8
A microwave preparation method of nanometer neodymium oxide comprises the following steps,
(1) surface treatment: adjusting the pH value of a neodymium salt solution with the concentration of 1.5mol/L to be alkaline, and adding polyacrylamide with the molar mass of 8% of the neodymium salt solution to obtain a neodymium-containing solution with surface treatment;
(2) precipitation reaction: dropwise adding a precipitator into the neodymium-containing solution subjected to surface treatment at the speed of 2.7L/min while stirring, and aging, filtering and washing to obtain a neodymium-containing precipitate; the precipitant is oxalate: carbonate radical: bicarbonate radical 1: 1.5: 0.2; the precipitating agent is: neodymium in a molar ratio of 1.1: 1;
(3) microwave calcination: putting the neodymium-containing precipitate into a microwave reactor, and carrying out microwave heating calcination for 3h at the frequency of 915 +/-50 MHz, the power of 4kw and the temperature of 1100 ℃ to obtain nano neodymium oxide powder; the microwave output mode comprises a continuous wave mode and a pulse wave mode.
While embodiments of the invention have been disclosed above, it is not intended to be limited to the uses set forth in the specification and examples. It can be applied to all kinds of fields suitable for the present invention. Additional modifications will readily occur to those skilled in the art. The invention is therefore not to be limited to the specific details described herein, without departing from the general concept as defined by the appended claims and their equivalents.
Claims (10)
1. A microwave preparation method of nanometer rare earth oxide is characterized in that: comprises the following steps of (a) carrying out,
(1) surface treatment: taking rare earth salt solution to adjust the pH value to be alkaline, and adding a surface auxiliary agent to obtain rare earth-containing solution for surface treatment;
(2) precipitation reaction: dropwise adding a precipitant into the rare earth-containing solution subjected to surface treatment while stirring, and aging, filtering and washing to obtain a rare earth precipitate;
(3) microwave calcination: and placing the rare earth precipitate into a microwave reactor for microwave heating and calcining to obtain the nano rare earth oxide powder.
2. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the rare earth salt solution is praseodymium salt, neodymium salt or praseodymium-neodymium salt; the concentration of the rare earth salt solution is 0.1-2 mol/L.
3. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the surface auxiliary agent in the step (1) is one of stearic acid, polyacrylamide, citric acid and sodium dodecyl sulfate.
4. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the addition amount of the surface additive is 5-15% of the molar mass of the rare earth salt solution.
5. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the precipitant in step (2) is any one or combination of oxalic acid, carbonic acid, ammonium bicarbonate, oxalate and carbonate, and when the precipitant is a combined precipitant, the ratio of oxalate: carbonate 1:0.2-1.8 or oxalate: carbonate radical: bicarbonate radical 0.8-1.5: 0.5-2: 0.1-0.5.
6. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the addition amount of the precipitant is as follows according to mol ratio: rare earth is added in a ratio of 1-3: 1.
7. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the precipitant is added at a rate of 0.5-3L/min.
8. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the frequency of microwave heating calcination in the step (3) is 915 +/-50 MHz or 2450 +/-50 MHz, and the power is 1-10 kw.
9. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the microwave heating calcination temperature is 800-1200 ℃, and the calcination time is 2-6 h.
10. The microwave preparation method of nano rare earth oxide according to claim 1, characterized in that: the microwave output mode comprises either one or two combination modes of continuous waves and pulse waves.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010330543.5A CN111634935A (en) | 2020-04-24 | 2020-04-24 | Microwave preparation method of nano rare earth oxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010330543.5A CN111634935A (en) | 2020-04-24 | 2020-04-24 | Microwave preparation method of nano rare earth oxide |
Publications (1)
Publication Number | Publication Date |
---|---|
CN111634935A true CN111634935A (en) | 2020-09-08 |
Family
ID=72324703
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010330543.5A Pending CN111634935A (en) | 2020-04-24 | 2020-04-24 | Microwave preparation method of nano rare earth oxide |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111634935A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114180613A (en) * | 2021-12-13 | 2022-03-15 | 包头稀土研究院 | Method for preparing rare earth oxide by recycling ammonia and carbon and application of rare earth oxide |
CN115010165A (en) * | 2022-05-20 | 2022-09-06 | 全南县新资源稀土有限责任公司 | Preparation method of rare earth carbonate and preparation method of rare earth oxide |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1417127A (en) * | 2002-12-16 | 2003-05-14 | 中国科学院长春应用化学研究所 | Prepn process of RE nano oxide |
CN1921935A (en) * | 2004-02-26 | 2007-02-28 | 罗狄亚化学公司 | Composition based on oxides of zirconium, praseodymium, lanthanum or neodymium, method for the preparation and use thereof in a catalytic system |
CN102161508A (en) * | 2011-02-12 | 2011-08-24 | 河北联合大学 | Method for synthesizing zinc vanadate micron/nano materials by adopting microwave radiation method |
CN102205985A (en) * | 2011-04-02 | 2011-10-05 | 南昌大学 | Preparation method for yttrium oxide with different specific surface area |
CN104973615A (en) * | 2015-06-26 | 2015-10-14 | 山东大学 | Microwave burning preparation method of nano gadolinium oxide powder |
CN105858706A (en) * | 2015-01-22 | 2016-08-17 | 湖南稀土金属材料研究院 | Method for preparing yttrium oxide powder |
CN106277021A (en) * | 2015-06-12 | 2017-01-04 | 常州卓煜新材料科技有限公司 | A kind of large-specific surface area nano Dineodymium trioxide preparation method |
CN106573792A (en) * | 2014-08-15 | 2017-04-19 | 稀土盐分离提纯有限公司 | Method for extraction and separation of rare earth elements |
CN108083316A (en) * | 2016-11-22 | 2018-05-29 | 厦门稀土材料研究所 | A kind of preparation method of nano rareearth oxidate powder body |
CN108217710A (en) * | 2018-01-24 | 2018-06-29 | 常州市卓群纳米新材料有限公司 | A kind of preparation method for being conducive to stablize neodymia particle size distribution |
CN108585015A (en) * | 2018-06-19 | 2018-09-28 | 四川江铜稀土有限责任公司 | A kind of method that microwave calcination prepares lanthana |
CN109019656A (en) * | 2018-09-28 | 2018-12-18 | 包头稀土研究院 | The production method of nano rareearth oxidate powder body |
-
2020
- 2020-04-24 CN CN202010330543.5A patent/CN111634935A/en active Pending
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1417127A (en) * | 2002-12-16 | 2003-05-14 | 中国科学院长春应用化学研究所 | Prepn process of RE nano oxide |
CN1921935A (en) * | 2004-02-26 | 2007-02-28 | 罗狄亚化学公司 | Composition based on oxides of zirconium, praseodymium, lanthanum or neodymium, method for the preparation and use thereof in a catalytic system |
CN102161508A (en) * | 2011-02-12 | 2011-08-24 | 河北联合大学 | Method for synthesizing zinc vanadate micron/nano materials by adopting microwave radiation method |
CN102205985A (en) * | 2011-04-02 | 2011-10-05 | 南昌大学 | Preparation method for yttrium oxide with different specific surface area |
CN106573792A (en) * | 2014-08-15 | 2017-04-19 | 稀土盐分离提纯有限公司 | Method for extraction and separation of rare earth elements |
CN105858706A (en) * | 2015-01-22 | 2016-08-17 | 湖南稀土金属材料研究院 | Method for preparing yttrium oxide powder |
CN106277021A (en) * | 2015-06-12 | 2017-01-04 | 常州卓煜新材料科技有限公司 | A kind of large-specific surface area nano Dineodymium trioxide preparation method |
CN104973615A (en) * | 2015-06-26 | 2015-10-14 | 山东大学 | Microwave burning preparation method of nano gadolinium oxide powder |
CN108083316A (en) * | 2016-11-22 | 2018-05-29 | 厦门稀土材料研究所 | A kind of preparation method of nano rareearth oxidate powder body |
CN108217710A (en) * | 2018-01-24 | 2018-06-29 | 常州市卓群纳米新材料有限公司 | A kind of preparation method for being conducive to stablize neodymia particle size distribution |
CN108585015A (en) * | 2018-06-19 | 2018-09-28 | 四川江铜稀土有限责任公司 | A kind of method that microwave calcination prepares lanthana |
CN109019656A (en) * | 2018-09-28 | 2018-12-18 | 包头稀土研究院 | The production method of nano rareearth oxidate powder body |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114180613A (en) * | 2021-12-13 | 2022-03-15 | 包头稀土研究院 | Method for preparing rare earth oxide by recycling ammonia and carbon and application of rare earth oxide |
JP2023087632A (en) * | 2021-12-13 | 2023-06-23 | 包頭稀土研究院 | Method of producing rare-earth oxide by recycling ammonium and carbon, and use of rare-earth oxide |
JP7335404B2 (en) | 2021-12-13 | 2023-08-29 | 包頭稀土研究院 | Method of preparing rare earth oxides by recycling ammonium and carbon and use of rare earth oxides |
CN114180613B (en) * | 2021-12-13 | 2024-04-12 | 包头稀土研究院 | Method for preparing rare earth oxide by recycling ammonia and carbon and application of rare earth oxide |
CN115010165A (en) * | 2022-05-20 | 2022-09-06 | 全南县新资源稀土有限责任公司 | Preparation method of rare earth carbonate and preparation method of rare earth oxide |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101234750B (en) | Method of preparing superfine micro-particle and nano granule | |
CN108946827B (en) | Ultra-small particle size nickel-cobalt-manganese hydroxide and preparation method thereof | |
CN108689422B (en) | Preparation method of large-specific-surface-area nano gadolinium oxide powder | |
CN111634935A (en) | Microwave preparation method of nano rare earth oxide | |
CN102560172A (en) | Method for preparing dispersion-strengthened copper with high strength and high conductivity | |
CN110980788A (en) | Method for preparing superfine dysprosium oxide | |
CN103962570A (en) | Preparation method of nickel nanopowder | |
CN109052450B (en) | Preparation method of high-purity gadolinium oxide | |
CN105161246A (en) | Nickel-zinc ferrite/polyacrylic acid nano-composite material and preparation method thereof | |
CN102491742A (en) | Method and apparatus for preparing manganese and copper co-doped ZnO diluted magnetic semiconductor material | |
CN113800574B (en) | Nickel-manganese-iron-aluminum-lithium positive electrode material and preparation method thereof | |
CN102557151B (en) | Method for preparing nanometer ferroferric oxide powder by reducing at one step | |
WO2024088057A1 (en) | Vanadium oxide and rare earth double-doped ferrite magnetic composite film slurry preparation process and coating method | |
CN116199270B (en) | Treatment process for reducing wastewater in cobalt oxide production process | |
CN103508492B (en) | Method for rapidly preparing NdWO4(OH) nanopowder | |
CN111533158A (en) | Microwave calcination preparation method of dysprosium oxide nano powder | |
CN111253152B (en) | Fast-attenuation high-light-efficiency scintillation material and preparation method thereof | |
CN103121723A (en) | Low-calcium-magnesium high-purity manganous-manganic oxide and preparation method for same | |
CN112877746A (en) | Method for preparing high-purity lutetium aluminum garnet precursor | |
CN101898785B (en) | Method for reducing content of Al2O3 in neodymium carbonate and praseodymium-neodymium carbonate product | |
CN102502782A (en) | Preparation method of chrome-manganese codope ZnO diluted magnetic semiconductor material and device | |
CN110526701A (en) | A kind of method that ferrite solid waste cycling and reutilization prepares electromagnetic wave absorbent material | |
CN108585823B (en) | Preparation method of monodisperse YAG microcrystalline powder | |
CN115159557B (en) | Preparation method of nano dysprosium oxide | |
CN116199251B (en) | Method for efficiently preparing gallium oxyhydroxide |
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 |