CN110606742B - TiO for nuclear power2-Gd2O3Burnable poison ceramic material and preparation method thereof - Google Patents
TiO for nuclear power2-Gd2O3Burnable poison ceramic material and preparation method thereof Download PDFInfo
- Publication number
- CN110606742B CN110606742B CN201911016644.9A CN201911016644A CN110606742B CN 110606742 B CN110606742 B CN 110606742B CN 201911016644 A CN201911016644 A CN 201911016644A CN 110606742 B CN110606742 B CN 110606742B
- Authority
- CN
- China
- Prior art keywords
- tio
- solution
- ceramic material
- nuclear power
- burnable poison
- 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.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/50—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on rare-earth compounds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/62605—Treating the starting powders individually or as mixtures
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/62605—Treating the starting powders individually or as mixtures
- C04B35/62645—Thermal treatment of powders or mixtures thereof other than sintering
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C3/00—Reactor fuel elements and their assemblies; Selection of substances for use as reactor fuel elements
- G21C3/42—Selection of substances for use as reactor fuel
- G21C3/58—Solid reactor fuel Pellets made of fissile material
- G21C3/62—Ceramic fuel
- G21C3/623—Oxide fuels
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3231—Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
- C04B2235/3232—Titanium oxides or titanates, e.g. rutile or anatase
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/656—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
- C04B2235/6562—Heating rate
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/656—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
- C04B2235/6567—Treatment time
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/658—Atmosphere during thermal treatment
- C04B2235/6581—Total pressure below 1 atmosphere, e.g. vacuum
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/658—Atmosphere during thermal treatment
- C04B2235/6582—Hydrogen containing atmosphere
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E30/00—Energy generation of nuclear origin
- Y02E30/30—Nuclear fission reactors
Abstract
The invention discloses TiO for nuclear power2‑Gd2O3The burnable poison ceramic material and the preparation method thereof solve the problem that TiO which can be effectively applied to nuclear power operation environment and effectively improve the safety and the economical efficiency of nuclear power is not found in the prior art2‑Gd2O3Problems with burnable poison materials. The invention comprises (1) preparing Gd (NO)3)3And Ti (NO)3)4Preparing saturated (NH)4)2CO3A solution; (2) will saturate (NH)4)2CO3Adding the solution into the mixed solution for reaction to obtain a precipitate after the reaction; (3) cleaning the precipitate, and drying to obtain precursor powder; (4) placing the precursor powder at 500-550 ℃, preserving heat for 5-7 h, taking out and grinding to obtain powder; (5) and pressing and molding the powder, and sintering to obtain a finished product. The invention has the advantages of high density, high strength, high inherent safety and the like, and is suitable for advanced nuclear power water-cooled power stacks.
Description
Technical Field
The invention relates to the field of composite ceramic materials, in particular to TiO for nuclear power2-Gd2O3A burnable poison ceramic material and a preparation method thereof.
Background
TiO2/B is widely adopted in nuclear power reactors at home and abroad, particularly in reactor cores of pressurized water reactor nuclear power stations4The C burnable poison material is used for controlling the initial reactivity of the reactor, realizing flattening the power distribution of the reactor core, improving the fuel consumption and prolonging the refueling period, thereby reducing the nuclear power operation cost and improving the operationSafety and reliability. However, with the increasing fuel consumption and core power of the advanced nuclear reactor of the new generation, Al2O3/B4C burnable poison materials not only accelerate swelling but also reduce their chemical stability, thereby affecting the safety and economics of nuclear reactor operation.
In order to solve the problems, the existing pressurized water reactor nuclear fuel element is designed by adopting a zirconium alloy cladding. The method for preparing the composite ceramic material at home and abroad mainly comprises a ball milling method, a powder metallurgy method and the like. However, the composite ceramic material prepared by the method has the defects of difficult internal uniformity control, difficult densification, more internal pores and defects and the like, and generates a large amount of dust in the preparation process, thereby polluting the environment and damaging the body health of personnel.
And, due to TiO2-Gd2O3When the porosity of the composite ceramic material is too large, water vapor can be adsorbed, so that the zirconium alloy cladding material is subjected to hydrogen embrittlement corrosion; TiO22Matrix and Gd2O3Degree of solid solution to TiO2-Gd2O3The service performance of the composite ceramic material under high temperature conditions also has important influence. Thus, TiO prepared by the existing method2-Gd2O3The burnable poison material can not further improve the safety and the economical efficiency of nuclear power operation; nor is there any document describing how to prepare TiO suitable for use in a nuclear fuel element of a hydropneumatic reactor2-Gd2O3A method of burnable poison materials.
Disclosure of Invention
The technical problem to be solved by the invention is as follows: TiO which can be effectively applied to nuclear power operation environment and can effectively improve the safety and the economical efficiency of nuclear power is not found in the prior art2-Gd2O3The problem of burnable poison material, and aims to provide TiO for nuclear power2-Gd2O3A burnable poison ceramic material and provides the TiO for nuclear power2-Gd2O3A method for preparing a burnable poison ceramic material.
The invention is realized by the following technical scheme:
TiO for nuclear power2-Gd2O3The preparation method of the burnable poison ceramic material is characterized by comprising the following steps:
(1) preparation of Gd (NO)3)3And Ti (NO)3)4Preparing saturated (NH)4)2CO3A solution;
(2) will saturate (NH)4)2CO3Adding the solution into the mixed solution for reaction to obtain a precipitate after the reaction;
(3) cleaning the precipitate, and drying to obtain precursor powder;
(4) placing the precursor powder at 500-550 ℃, preserving heat for 5-7 h, taking out and grinding to obtain powder;
(5) and pressing and molding the powder, and sintering to obtain a finished product.
The finished product prepared by the method is TiO2-Gd2O3Burnable poison material, finished product of the invention and Al2O3/B4C has the following advantages compared with the prior art: one is a lower swelling rate; second is TiO2Matrix and Gd2O3A readily formable solid solution minimizes the problem of homogeneity of burnable poison materials; III is TiO2The substrate has excellent chemical stability to the cladding alloy and primary coolant.
And, TiO prepared by the coprecipitation method of the present invention2-Gd2O3The burnable poison material can form a uniform displacement type solid solution, has the characteristics of high density, high strength and the like, and can overcome the defect that the zirconium alloy cladding material is subjected to hydrogen embrittlement corrosion due to the fact that water vapor is adsorbed when the porosity is too large. Also, the TiO prepared by the method of the present invention2-Gd2O3The burnable poison material has the advantages of good uniformity, purity and crystal structure of chemical components of the obtained material, low sintering temperature, higher mechanical strength and the like. Through detection, the TiO prepared by the invention2-Gd2O3The density of the burnable poison material is greater than 94.8% T.D.
Thus, the high density, good microstructure TiO of the present invention2-Gd2O3The burnable poison material lays a foundation for the research of the burnable poison material with high inherent safety for nuclear power, provides technical support, and has higher academic value and engineering application value.
Further, the sintering in the step (5) is vacuum sintering, and the sintering conditions are as follows: vacuum degree of 10-2～10-3Pa, a sintering temperature of 1600-1650 ℃, a heat preservation time of 3-4H, a temperature rise rate of 30 ℃/min, and a sintering atmosphere of H2。
Further, the drying conditions of the step (3) are as follows: drying for 5-6 h at 150-170 ℃.
Further, in the step (3), the precipitate is washed by absolute ethyl alcohol for 2-3 times.
Further, the reaction temperature of the step (2) is 50-55 ℃, and the reaction process is saturated (NH)4)2CO3The adding speed of the solution is 2-4 ml/min, and the pH value of the reaction solution is kept at 6.5-8.5 in the reaction process.
Further, Gd (NO)3)3And Al (NO)3)3The preparation process of the mixed solution comprises the following steps:
gd with a purity of 99.9 percent2O3Drying the powder, adding deionized water, and dissolving with concentrated nitric acid under stirring to obtain Gd (NO)3)3A solution;
adding deionized water and absolute ethyl alcohol into nano titanium oxide powder, and adding concentrated nitric acid to dissolve the mixture under the condition of stirring to prepare a titanium sol solution;
mixing prepared Gd (NO)3)3The solution is dropped into the titanium sol solution and is continuously stirred for 20-25 min, and Gd (NO) can be formed3)3And Ti (NO)3)4The mixed solution of (1).
Further, the saturation (NH)4)2CO3The preparation process of the solution is as follows: analytically pure solid ammonium carbonate is put into a container, deionized water is added and the mixture is continuously addedStirring to make saturated (NH)4)2CO3And (3) solution.
Further, the step (2) is saturated with (NH)4)2CO3After the solution addition was completed, anhydrous ethanol was added.
TiO for nuclear power2-Gd2O3The burnable poison ceramic material is the TiO for nuclear power2-Gd2O3The finished product is prepared by the preparation method of the burnable poison ceramic material.
Wherein, TiO2-Gd2O3TiO in burnable poison ceramic material2The mass percentage of (B) is less than 15%.
Compared with the prior art, the invention has the following advantages and beneficial effects:
1. TiO produced by the invention2-Gd2O3The density of the burnable poison material is more than 95.5 percent T.D, the mechanical property (bending strength and fracture toughness) is excellent, the burnable poison material is suitable for an advanced nuclear power water-cooled power reactor, and the intrinsic safety is high;
2. the invention has no strict requirements on process equipment, is easy to realize, and has good sintering performance and good microstructure.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is further described in detail below with reference to examples, and the exemplary embodiments and descriptions thereof are only used for explaining the present invention and are not used as limitations of the present invention.
Example 1
TiO2-Gd for nuclear power2O3A method of preparing a burnable poison ceramic material, comprising:
firstly, drying the nano titanium oxide powder for 3h at 500 ℃, weighing 100g of nano titanium oxide powder, putting the nano titanium oxide powder into a beaker, adding 100ml of deionized water and 30ml of absolute ethyl alcohol into the beaker, and adding 20ml of concentrated nitric acid into the beaker under the condition of rapid stirring to dissolve the mixture to obtain a stable titanium sol solution. Weighing 5.3g of dried gadolinium trioxide powder according to the mass ratio of gadolinium trioxide in the materialPlacing into a dissolving tank, adding 30ml deionized water, adding 7ml concentrated nitric acid under rapid stirring for dissolving for 28min, and filtering to obtain clear filtrate (Gd (NO)3)3And (3) solution. Mixing prepared Gd (NO) under the condition of rapid stirring3)3Slowly dropping the solution into the titanium sol solution, and continuously stirring for 25min to form uniform Gd (NO)3)3And Ti (NO)3)4The solution was mixed. 100g of analytically pure solid ammonium carbonate are weighed into a beaker, deionized water is added to the beaker and the mixture is stirred rapidly to form saturated (NH)4)2CO3And (3) solution.
In the second step, Gd (NO) is added3)3And Ti (NO)3)4Adding the mixed solution into a precipitation tank, starting stirring, heating to the reaction temperature of 50 ℃, and then adding saturated (NH)4)2CO3Dripping the solution into a precipitation tank at a speed of 2ml/min, adjusting the pH value of the mixed solution to keep the pH value at about 7, carrying out strong stirring while dripping to fully react, adding 30ml of absolute ethyl alcohol after the addition is finished, and precipitating the mixed solution after a period of time to completely react and lose fluidity. And then filtering the precipitate to obtain a filter cake, washing the filter cake for 2 times by using absolute ethyl alcohol, and drying at 150 ℃ for 6 hours to obtain precursor powder.
Thirdly, keeping the dried precursor powder in a box furnace at 500 ℃ for 7h, taking out after air cooling and grinding to obtain TiO2-Gd2O3And (3) powder. Finally, the dried and calcined powder is pressed and molded (the molding pressure is 50MPa, the sample size is 50mm multiplied by 10mm) under the vacuum degree of 2.5 multiplied by 10-3Pa, sintering temperature: 1600 ℃, the heat preservation time is 4H, the heating rate is 30 ℃/min, and the sintering atmosphere is H2Vacuum sintering under the conditions of (1) to obtain compact TiO2-Gd2O3A burnable poison ceramic material.
Example 2
The difference between this embodiment and embodiment 1 is that the specific process parameters of each step in this embodiment are different, and the specific settings are as follows:
in the second step, the pH of the mixed solution was maintained at about 8 during the reaction.
In the third step, the heat preservation temperature of the precursor powder is 520 ℃, and the heat preservation time is 6 hours; the vacuum sintering temperature is 1630 ℃, and the heat preservation time is 3.5 h.
Example 3
The difference between this embodiment and embodiment 1 is that the specific process parameters of each step in this embodiment are different, and the specific settings are as follows:
in the third step, the heat preservation temperature of the precursor powder is 550 ℃, and the heat preservation time is 5 hours; the vacuum sintering temperature is 1650 ℃, and the heat preservation time is 3 h.
Example 4
This example differs from example 1 in that Gd is present in this example2O3In different weight percentages, TiO in this example2-Gd2O3TiO in burnable poison ceramic material2Is 5% by weight.
Example 5
This example differs from example 1 in that Gd is present in this example2O3In different weight percentages, TiO in this example2-Gd2O3TiO in burnable poison ceramic material2Is 13% by weight.
Example 6
This example is a comparative example of examples 1 to 3, and the difference between this example and example 1 is that the process parameters of the steps in this example are different, and the specific settings are as follows:
in the second step, the pH of the mixed solution was maintained at about 6 during the reaction.
In the third step, the heat preservation temperature of the precursor powder is 570 ℃, and the heat preservation time is 4 hours; the vacuum sintering temperature is 1670 ℃, and the heat preservation time is 3 hours.
Example 7
This example is a comparative example of examples 1 to 3, and the difference between this example and example 1 is that the process parameters of the steps in this example are different, and the specific settings are as follows:
in the second step, the pH of the mixed solution was maintained at about 9 during the reaction.
In the third step, the heat preservation temperature of the precursor powder is 480 ℃, and the heat preservation time is 8 hours; the vacuum sintering temperature is 1580 ℃, and the heat preservation time is 5 hours.
TiO prepared by the method described in examples 1-72-Gd2O3The burnable poison ceramic material is detected, the detected items comprise the detection of compactness, bending strength and fracture toughness, and the detection results are shown in Table 1
TABLE 1
| Compactness (relative density) | Bending strength | Fracture toughness | |
| Example 1 | 96.0％ | 300.8MPa | 4.02MPa.m1/2 |
| Example 2 | 96.8％ | 301.5MPa | 4.04MPa.m1/2 |
| Example 3 | 95.9％ | 300.6MPa | 4.02MPa.m1/2 |
| Example 4 | 95.7％ | 300.2MPa | 4.03MPa.m1/2 |
| Example 5 | 96.5％ | 301.1MPa | 3.98MPa.m1/2 |
| Example 6 | 95.6％ | 299.1MPa | 3.96MPa.m1/2 |
| Example 7 | 95.5％ | 298.8MPa | 3.97MPa.m1/2 |
As is clear from the results shown in Table 1, TiO produced by the method of the present invention2-Gd2O3The burnable poison ceramic material has higher density and excellent mechanical property, and can effectively lay a foundation for the research of the burnable poison material with high inherent safety for nuclear power and provide technical support.
The above-mentioned embodiments are intended to illustrate the objects, technical solutions and advantages of the present invention in further detail, and it should be understood that the above-mentioned embodiments are merely exemplary embodiments of the present invention, and are not intended to limit the scope of the present invention, and any modifications, equivalent substitutions, improvements and the like made within the spirit and principle of the present invention should be included in the scope of the present invention.
Claims (9)
1. TiO for nuclear power2-Gd2O3The preparation method of the burnable poison ceramic material is characterized by comprising the following steps:
(1) preparation of Gd (NO)3)3And Ti (NO)3)4Preparing saturated (NH)4)2CO3A solution;
(2) will saturate (NH)4)2CO3Adding the solution into the mixed solution for reaction to obtain a precipitate after the reaction;
(3) cleaning the precipitate, and drying to obtain precursor powder;
(4) placing the precursor powder at 500-550 ℃, preserving heat for 5-7 h, taking out and grinding to obtain powder;
(5) pressing and molding the powder, and sintering to obtain a finished product;
the reaction temperature of the step (2) is 50-55 ℃, and the reaction process is saturated (NH)4)2CO3The adding speed of the solution is 2-4 ml/min, and the pH value of the reaction solution is kept at 6.5-8.5 in the reaction process.
2. TiO for nuclear power according to claim 12-Gd2O3The preparation method of the burnable poison ceramic material is characterized in that the sintering in the step (5) is vacuum sintering, and the sintering conditions are as follows: vacuum degree of 10-2～10-3Pa, a sintering temperature of 1600-1650 ℃, a heat preservation time of 3-4H, a temperature rise rate of 30 ℃/min, and a sintering atmosphere of H2。
3. TiO for nuclear power according to claim 12-Gd2O3The preparation method of the burnable poison ceramic material is characterized in that the drying conditions in the step (3) are as follows: drying for 5-6 h at 150-170 ℃.
4. According to the claims3 the TiO for nuclear power2-Gd2O3The preparation method of the burnable poison ceramic material is characterized in that in the step (3), the precipitate is cleaned by absolute ethyl alcohol for 2-3 times.
5. TiO for nuclear power according to claim 12-Gd2O3The preparation method of the burnable poison ceramic material is characterized in that Gd (NO)3)3And Al (NO)3)3The preparation process of the mixed solution comprises the following steps:
gd with a purity of 99.9 percent2O3Drying the powder, adding deionized water, and dissolving with concentrated nitric acid under stirring to obtain Gd (NO)3)3A solution;
adding deionized water and absolute ethyl alcohol into nano titanium oxide powder, and adding concentrated nitric acid to dissolve the mixture under the condition of stirring to prepare a titanium sol solution;
mixing prepared Gd (NO)3)3The solution is dropped into the titanium sol solution and is continuously stirred for 20-25 min, and Gd (NO) can be formed3)3And Ti (NO)3)4The mixed solution of (1).
6. TiO for nuclear power according to claim 12-Gd2O3The method for preparing the burnable poison ceramic material is characterized in that the saturated (NH)4)2CO3The preparation process of the solution is as follows:
analytically pure solid ammonium carbonate is placed in a container, deionized water is added and stirring is continued until saturation (NH)4)2CO3And (3) solution.
7. TiO for nuclear power according to claim 12-Gd2O3The preparation method of the burnable poison ceramic material is characterized in that (NH) is saturated in the step (2)4)2CO3After the solution addition was completed, anhydrous ethanol was added.
8. TiO for nuclear power2-Gd2O3The burnable poison ceramic material is characterized by being a finished product prepared by the preparation method of any one of claims 1 to 7.
9. TiO for nuclear power according to claim 82-Gd2O3Burnable poison ceramic material, characterized in that the TiO is2-Gd2O3TiO in burnable poison ceramic material2The mass percentage of (B) is less than 15%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201911016644.9A CN110606742B (en) | 2019-10-24 | 2019-10-24 | TiO for nuclear power2-Gd2O3Burnable poison ceramic material and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201911016644.9A CN110606742B (en) | 2019-10-24 | 2019-10-24 | TiO for nuclear power2-Gd2O3Burnable poison ceramic material and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN110606742A CN110606742A (en) | 2019-12-24 |
| CN110606742B true CN110606742B (en) | 2022-02-22 |
Family
ID=68895086
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201911016644.9A Active CN110606742B (en) | 2019-10-24 | 2019-10-24 | TiO for nuclear power2-Gd2O3Burnable poison ceramic material and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN110606742B (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102947890A (en) * | 2010-05-11 | 2013-02-27 | 钍能源股份有限公司 | Fuel assembly |
| CN103007302A (en) * | 2012-12-12 | 2013-04-03 | 中国科学院宁波材料技术与工程研究所 | Gd2O3-TiO2 composite nanoparticle as well as preparation method and application thereof |
| CN103449811A (en) * | 2013-08-23 | 2013-12-18 | 中国核动力研究设计院 | Co-precipitation preparation method of ZrO2/Gd203 composite ceramic material for nuclear power |
| CN104751903A (en) * | 2015-03-11 | 2015-07-01 | 中国核动力研究设计院 | TiO2 doped UO2-10wt% Gd2O3 burnable poison and preparation method of TiO2 doped UO2-10wt% Gd2O3 burnable poison |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03205597A (en) * | 1990-01-05 | 1991-09-09 | Nippon Nuclear Fuel Dev Co Ltd | Production of nuclear fuel pellet of mixed oxide |
-
2019
- 2019-10-24 CN CN201911016644.9A patent/CN110606742B/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102947890A (en) * | 2010-05-11 | 2013-02-27 | 钍能源股份有限公司 | Fuel assembly |
| CN103007302A (en) * | 2012-12-12 | 2013-04-03 | 中国科学院宁波材料技术与工程研究所 | Gd2O3-TiO2 composite nanoparticle as well as preparation method and application thereof |
| CN103449811A (en) * | 2013-08-23 | 2013-12-18 | 中国核动力研究设计院 | Co-precipitation preparation method of ZrO2/Gd203 composite ceramic material for nuclear power |
| CN104751903A (en) * | 2015-03-11 | 2015-07-01 | 中国核动力研究设计院 | TiO2 doped UO2-10wt% Gd2O3 burnable poison and preparation method of TiO2 doped UO2-10wt% Gd2O3 burnable poison |
Also Published As
| Publication number | Publication date |
|---|---|
| CN110606742A (en) | 2019-12-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN107322002B (en) | Rare earth oxide doped tungsten-based composite powder and preparation method thereof | |
| CN113289693B (en) | Ammonia decomposition catalyst and preparation method and application thereof | |
| CN106630985B (en) | A kind of positive lithium metasilicate ceramic bead of tritium proliferation nanostructure and preparation method thereof | |
| CN108554407B (en) | Nano copper-based catalyst and preparation method thereof | |
| CN112675865B (en) | High-activity and high-stability supported nickel catalyst and preparation method and application thereof | |
| CN108658038B (en) | Based on LiAlH4Hydrogen storage material and method for producing the same | |
| CN101894594B (en) | Sub-stoichiometric UO2-xPreparation process of annular core block | |
| CN110606742B (en) | TiO for nuclear power2-Gd2O3Burnable poison ceramic material and preparation method thereof | |
| CN110729064B (en) | Al for nuclear power2O3-Gd2O3Burnable poison ceramic material and preparation method thereof | |
| CN110218092B (en) | UO added with trace elements2-ZrO2Ceramic material and preparation method thereof | |
| CN108525668B (en) | Preparation method of sepiolite nanofiber loaded cobalt-aluminum composite oxide | |
| CN102416475B (en) | Method for preparing nuclear functional material tungsten-tantalum alloy plate | |
| CN115073183B (en) | High-entropy boride nano powder and sol-gel preparation method thereof | |
| CN103449811B (en) | Co-precipitation preparation method of ZrO2/Gd203 composite ceramic material for nuclear power | |
| CN112694331B (en) | Method for preparing uranium dioxide composite fuel pellet by doping graphene oxide | |
| CN114835492A (en) | Rare earth-based zirconium-hafnium composite ceramic material and preparation method and application thereof | |
| CN103342389A (en) | Bi2WO6 with ordered macrostructure and preparation method thereof | |
| CN109382113B (en) | Perovskite type oxide catalyst, preparation method and application thereof | |
| CN110255614B (en) | Stable zirconia powder and preparation method and application thereof | |
| CN109529852A (en) | Nanoscale Ni-Fe/Al2O3 catalyst and its preparation method and application | |
| CN112316948B (en) | Method for preparing amorphous catalyst for methanation | |
| CN104795112B (en) | A kind of CaO doping UO2 10wt%Gd2O3 burnable poisons and preparation method thereof | |
| CN113753948B (en) | Method for preparing nano polycrystalline zirconia by ultrahigh pressure/high temperature phase change method | |
| CN115971011B (en) | High-entropy composite oxide hydrogen-resistant coating and preparation method thereof | |
| RU2734692C1 (en) | Method of producing fuel compositions based on uranium dioxide with the addition of a burnable neutron absorber |
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 |