CN104264087A - Preparation method for Zr (zirconium)-Nb (niobium)-Cu (copper) system alloy - Google Patents

Preparation method for Zr (zirconium)-Nb (niobium)-Cu (copper) system alloy Download PDF

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CN104264087A
CN104264087A CN201410548854.3A CN201410548854A CN104264087A CN 104264087 A CN104264087 A CN 104264087A CN 201410548854 A CN201410548854 A CN 201410548854A CN 104264087 A CN104264087 A CN 104264087A
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cold rolling
annealing
time
alloy
preparation
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CN104264087B (en
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柏广海
王荣山
张晏玮
梅金娜
刘二伟
耿建桥
杜晨曦
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China General Nuclear Power Corp
CGN Power Co Ltd
Suzhou Nuclear Power Research Institute Co Ltd
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China General Nuclear Power Corp
CGN Power Co Ltd
Suzhou Nuclear Power Research Institute Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/16Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of other metals or alloys based thereon
    • C22F1/18High-melting or refractory metals or alloys based thereon
    • C22F1/186High-melting or refractory metals or alloys based thereon of zirconium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C16/00Alloys based on zirconium

Abstract

The invention relates to a preparation method for a Zr (zirconium)-Nb (niobium)-Cu (copper) system alloy. The preparation method includes the steps of forging, quenching, hot extrusion, primary annealing, primary cold rolling and annealing, secondary cold rolling and annealing, and tertiary cold rolling and annealing, wherein in the primary cold rolling and annealing process, a workpiece after the primary annealing is treated with primary cold rolling, and treated with annealing treatment within a temperature range of 500 to 550 DEG C after the deformation reaches 50 to 70 percent; in the secondary cold rolling and annealing process, the workpiece after the primary cold rolling and annealing is treated with secondary cold rolling, and is treated with annealing treatment within a temperature range of 500 to 550 DEG C after the deformation reaches 50 to 70 percent; in the tertiary cold rolling and annealing process, the workpiece after the secondary cold rolling and annealing is treated with tertiary cold rolling, and is treated with annealing treatment within a temperature range of 450 to 520 DEG C after the deformation reaches 50 to 70 percent. Second-phrase particles of the Zr-Nb-Cu system alloy prepared through the method are distributed in a fine and dispersed manner; the corrosion resistance of the alloy prepared through the method is over 25 percent higher than that of alloys prepared through the traditional technique.

Description

The preparation method of a kind of Zr-Nb-Cu system alloy
Technical field
The invention belongs to alloy heat processing technique technical field, be specifically related to the preparation method of a kind of Zr-Nb-Cu system alloy.
Background technology
Zirconium alloy is light water reactor dyestuff cladding material, and the performance of zirconium alloy cladding determines the burnup of nuclear fuel, and the economy of nuclear power is also closely related with it, therefore has higher requirement to the performance of Reactor fuel element cladding material zirconium alloy.The corrosion resistance nature that the new zirconium alloy of commercial applications is as good in M5, Zirlo and E110 have at present.Domestic also at exploitation N18, N36 and C7 new zirconium alloy.Because C7 zirconium alloy with the addition of a small amount of Cu element on Zr-1Nb alloy basis, with Zr-Nb alloy phase ratio, its matrix α zr/ β zrall can there is considerable change in the behavior of growing up of phase transformation and second phase particles.And the comparatively large and skewness of the Zr-Nb-Cu system alloy second phase particles size that the complete processing of prior art is prepared, affect the corrosion resistance nature of alloy.
Summary of the invention
Technical problem to be solved by this invention overcomes the deficiencies in the prior art, the preparation method of a kind of Zr-Nb-Cu system alloy is provided, the distribution of the second phase particles of Zr-Nb-Cu system alloy prepared by the method less and even dispersion, makes the corrosion resistance nature of alloy significantly improve.
For solving above technical problem, the present invention adopts following technical scheme:
A preparation method for Zr-Nb-Cu system alloy, described preparation method comprises the following steps:
(1) forge: the zirconium alloy product containing Nb and Cu element is forged at 800 ~ 900 DEG C;
(2) quench: quench after the product after step (1) being forged is incubated 20 ~ 40min at 1000 ~ 1050 DEG C;
(3) hot extrusion: the product after step (2) being quenched carries out hot extrusion at 550 ~ 600 DEG C;
(4) anneal first: the product after step (3) hot extrusion is annealed at 500 ~ 550 DEG C;
(5) three cold rolling and annealing: the product after step (4) being annealed first carries out three cold rolling and annealing again, obtained Zr-Nb-Cu system alloy;
In step (5), described three concrete steps that are cold rolling and annealing are as follows:
First time is cold rolling and anneal: it is cold rolling that the product after described step (4) being annealed first carries out first time, after deflection reaches 50 ~ 70%, at 500 ~ 550 DEG C, carries out anneal;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 50 ~ 70%, carry out anneal at 500 ~ 550 DEG C;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 50 ~ 70%, carry out anneal at 450 ~ 520 DEG C.
Described first time, cold rolling and in annealing annealing time was 0.5 ~ 1.5 hour.
Cold rolling and in annealing the annealing time of described second time is 0.5 ~ 1.5 hour.
Described third time, cold rolling and in annealing annealing time was 1.5 ~ 4 hours.
Described annealing time is first 2 ~ 4 hours.
Described Zr-Nb-Cu system alloy is that Zr and inevitable impurity form by Nb 0.6-1.2wt.%, Cu 0.01-0.1wt.%, surplus.
Described Zr-Nb-Cu system alloy is Zr-1Nb-0.01Cu alloy or Zr-1.1Nb-0.05Cu alloy.
Described Zr-Nb-Cu system second phase particles in alloy is small and dispersed distribution.
Due to the enforcement of technique scheme, the present invention compared with prior art tool has the following advantages:
The Zr-Nb-Cu system alloy phase ratio prepared with traditional preparation methods, the Zr-Nb-Cu system alloy that preparation method of the present invention prepares, the distribution of the size of particles of its second-phase less and even dispersion, corrosion resistance nature improves more than 25%.
Accompanying drawing explanation
The second phase particles distribution metallograph of the Zr-1Nb-0.01Cu alloy of Fig. 1 prepared by embodiment 1;
The second phase particles distribution metallograph of the Zr-1Nb-0.01Cu alloy of Fig. 2 prepared by embodiment 2;
The second phase particles distribution metallograph of the Zr-1.1Nb-0.05Cu alloy of Fig. 3 prepared by embodiment 3;
The second phase particles distribution metallograph of the Zr-1Nb-0.01Cu alloy of Fig. 4 prepared by comparative example 1;
The second phase particles distribution metallograph of the Zr-1Nb-0.01Cu alloy of Fig. 5 prepared by comparative example 2;
The second phase particles distribution metallograph of the Zr-1.1Nb-0.05Cu alloy of Fig. 6 prepared by comparative example 3;
Fig. 7 is the surrosion graphic representation of the prepared Zr-1Nb-0.01Cu alloy of embodiment 1 and comparative example 1;
Fig. 8 is the surrosion graphic representation of the prepared Zr-1Nb-0.01Cu alloy of embodiment 2 and comparative example 2;
Fig. 9 is the surrosion graphic representation of the prepared Zr-1.1Nb-0.05Cu alloy of embodiment 3 and comparative example 3.
Embodiment
Below by specific embodiment, the invention will be further described.
The preparation method of Zr-Nb-Cu system of the present invention alloy, comprises the following steps:
(1) forge: the zirconium alloy product containing Nb and Cu element is forged at 800 ~ 900 DEG C;
(2) quench: carry out quench (quenching can be carried out in atmosphere) after the product after step (1) being forged is incubated 20 ~ 40min at 1000 ~ 1050 DEG C;
(3) hot extrusion: the product after step (2) being quenched carries out hot extrusion at 550 ~ 600 DEG C;
(4) anneal first: the product after step (3) hot extrusion is annealed at 500 ~ 550 DEG C, anneals 2 ~ 4 hours;
(5) three cold rolling and annealing: the product after step (4) being annealed first carries out three cold rolling and annealing again, obtained Zr-Nb-Cu system alloy;
In step (5), three times concrete steps that are cold rolling and annealing are as follows:
First time is cold rolling and anneal: it is cold rolling that the product after step (4) being annealed first carries out first time, after deflection reaches 50 ~ 70%, at 500 ~ 550 DEG C, carries out anneal, anneals 0.5 ~ 1.5 hour;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 50 ~ 70%, carry out anneal at 500 ~ 550 DEG C, anneal 0.5 ~ 1.5 hour;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 50 ~ 70%, carry out anneal at 450 ~ 520 DEG C, anneal 1.5 ~ 4 hours.
Described first time, cold rolling and in annealing annealing time was 0.5 ~ 1.5 hour.
Cold rolling and in annealing the annealing time of described second time is 0.5 ~ 1.5 hour.
Described third time, cold rolling and in annealing annealing time was 1.5 ~ 4 hours.
Described annealing time is first 2 ~ 4 hours.
Embodiment 1
The present embodiment provides a kind of preparation method of Zr-1Nb-0.01Cu alloy, consisting of of this Zr-1Nb-0.01Cu alloy: Nb1wt%, Cu0.01wt%, Zr surplus and inevitably impurity, and this preparation method comprises the following steps:
(1) forge: the zirconium alloy product containing Nb and Cu element is forged at 800 ~ 900 DEG C;
(2) quench: quench after the product after step (1) being forged is incubated 20min at 1020 DEG C;
(3) hot extrusion: the product after step (2) being quenched carries out hot extrusion at 550 ~ 600 DEG C;
(4) anneal first: the product after step (3) hot extrusion is annealed at 550 DEG C, anneals 2 hours;
(5) three cold rolling and annealing: the product after step (4) being annealed first carries out three cold rolling and annealing again, obtained Zr-Nb-Cu system alloy;
In step (5), three times concrete steps that are cold rolling and annealing are as follows:
First time is cold rolling and anneal: it is cold rolling that the product after step (4) being annealed first carries out first time, after deflection reaches 55%, at 520 DEG C, carries out anneal, anneals 1 hour;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 55%, carry out anneal at 520 DEG C, anneal 1 hour;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 65%, carry out anneal at 520 DEG C, anneal 2 hours.
Embodiment 2
The present embodiment provides a kind of preparation method of Zr-1Nb-0.01Cu alloy, consisting of of this Zr-1Nb-0.01Cu alloy: Nb1wt%, Cu0.01wt%, Zr surplus and inevitably impurity, and this preparation method comprises the following steps:
(1) forge: the zirconium alloy product containing Nb and Cu element is forged at 800 ~ 900 DEG C;
(2) quench: quench after the product after step (1) being forged is incubated 20min at 1020 DEG C;
(3) hot extrusion: the product after step (2) being quenched carries out hot extrusion at 550 ~ 600 DEG C;
(4) anneal first: the product after step (3) hot extrusion is annealed at 550 DEG C, anneals 2 hours;
(5) three cold rolling and annealing: the product after step (4) being annealed first carries out three cold rolling and annealing again, obtained Zr-Nb-Cu system alloy;
In step (5), three times concrete steps that are cold rolling and annealing are as follows:
First time is cold rolling and anneal: it is cold rolling that the product after step (4) being annealed first carries out first time, after deflection reaches 55%, at 550 DEG C, carries out anneal, anneals 1 hour;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 55%, carry out anneal at 550 DEG C, anneal 1 hour;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 65%, carry out anneal at 460 DEG C, anneal 4 hours.
Embodiment 3
The present embodiment provides a kind of preparation method of Zr-1.1Nb-0.05Cu alloy, consisting of of this Zr-1.1Nb-0.05Cu alloy: Nb1.1wt%, Cu0.05wt%, Zr surplus and inevitably impurity, and this preparation method comprises the following steps:
(1) forge: the zirconium alloy product containing Nb and Cu element is forged at 800 ~ 900 DEG C;
(2) quench: quench after the product after step (1) being forged is incubated 20min at 1020 DEG C;
(3) hot extrusion: the product after step (2) being quenched carries out hot extrusion at 550 ~ 600 DEG C;
(4) anneal first: the product after step (3) hot extrusion is annealed at 550 DEG C, anneals 2 hours;
(5) three cold rolling and annealing: the product after step (4) being annealed first carries out three cold rolling and annealing again, obtained Zr-Nb-Cu system alloy;
In step (5), three times concrete steps that are cold rolling and annealing are as follows:
First time is cold rolling and anneal: it is cold rolling that the product after step (4) being annealed first carries out first time, after deflection reaches 55%, at 540 DEG C, carries out anneal, anneals 1 hour;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 55%, carry out anneal at 540 DEG C, anneal 1 hour;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 65%, carry out anneal at 520 DEG C, anneal 2 hours.
Temperature during three times in the preparation method of traditional Zr-Nb-Cu alloy cold rolling and annealing cold roller and deformed is higher, and annealing time is longer, i.e. (a) first cold rolling and annealing: after cold rolling reduction reaches 50 ~ 60%, anneal 2-4 hour at 560-600 DEG C; B () second time is cold rolling and anneal: after cold rolling reduction reaches 50-60%, anneal 2-4 hour at 560-600 DEG C; C () third time is cold rolling and anneal: after cold rolling reduction reaches 50-60%, anneal 8-10 hour at 560-600 DEG C.Illustrate below by comparative example:
Comparative example 1
This comparative example provides a kind of preparation method of Zr-1Nb-0.01Cu alloy, consisting of of this Zr-1Nb-0.01Cu alloy: Nb1wt%, Cu0.01wt%, Zr surplus and inevitably impurity, this preparation method is except step (5) three times is cold rolling and except annealing process, all the other steps (i.e. step (1) ~ (4)) are identical with embodiment 1.
In the step (5) of this comparative example, three times concrete steps that are cold rolling and annealing are as follows:
First time cold rolling and annealing: the product after step (4) being annealed first carries out first cold rolling, after deflection reaches 55%, carries out anneal at 580 DEG C, anneals 4 hours;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 55%, carry out anneal at 580 DEG C, anneal 4 hours;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 65%, carry out anneal at 580 DEG C, anneal 8 hours.
Comparative example 2
This comparative example provides a kind of preparation method of Zr-1Nb-0.01Cu alloy, consisting of of this Zr-1Nb-0.01Cu alloy: Nb1wt%, Cu0.01wt%, Zr surplus and inevitably impurity, this preparation method is except step (5) three times is cold rolling and except annealing process, all the other steps are identical with embodiment 2 with (i.e. step (1) ~ (4)).
In the step (5) of this comparative example, three times concrete steps that are cold rolling and annealing are as follows:
First time cold rolling and annealing: the product after step (4) being annealed first carries out first cold rolling, after deflection reaches 55%, carries out anneal at 580 DEG C, anneals 2 hours;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 55%, carry out anneal at 580 DEG C, anneal 2 hours;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 65%, carry out anneal at 580 DEG C, anneal 10 hours.
Comparative example 3
This comparative example provides a kind of preparation method of Zr-1.1Nb-0.05Cu alloy, consisting of of this Zr-1.1Nb-0.05Cu alloy: Nb1.1wt%, Cu0.05wt%, Zr surplus and inevitably impurity, this preparation method is except step (5) three times is cold rolling and except annealing process, all the other steps (i.e. step (1) ~ (4)) are identical with embodiment 3.
In the step (5) of this comparative example, three times concrete steps that are cold rolling and annealing are as follows:
First time cold rolling and annealing: the product after step (4) being annealed first carries out first cold rolling, after deflection reaches 55%, carries out anneal at 560 DEG C, anneals 4 hours;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 55%, carry out anneal at 560 DEG C, anneal 4 hours;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 65%, carry out anneal at 560 DEG C, anneal 10 hours.
Carry out metallurgical analysis to the Zr-Nb-Cu alloy prepared by embodiment 1 ~ 3 and comparative example 1 ~ 3, result is as shown in Fig. 1 ~ 6.
Comparison diagram 1 and Fig. 4, the second phase particles of embodiment 1 is small and dispersed distribution, and particle average size is 45.1nm; The second-phase size of comparative example 1 is comparatively large, and distribution of sizes is uneven, and particle average size is 60.2nm.
Comparison diagram 2 and Fig. 5, the second phase particles of embodiment 2 is small and dispersed distribution, and particle average size is 42.4nm; The second-phase size of comparative example 2 is comparatively large, and distribution of sizes is uneven, and particle average size is 67.1nm.
Comparison diagram 3 and Fig. 6, the second phase particles of embodiment 3 is small and dispersed distribution, and particle average size is 39.1nm; The second-phase size of comparative example 3 is comparatively large, and distribution of sizes is uneven, and particle average size is 58.7nm.
From above-mentioned comparing result, compare traditional technology, adopt preparation method of the present invention, in zirconium alloy, second phase particles thinning effect is obvious, and the mean sizes of second phase particles reduces more than 25%.
Corrosion resistance nature test is carried out to the Zr-Nb-Cu alloy prepared by embodiment 1 ~ 3 and comparative example 1 ~ 3, draws surrosion curve, as shown in Fig. 7 ~ 9.The corrosive medium adopted is 360 ° of C/18.6 MPa/3.5 ppm Li+1000 ppm B aqueous solution.
As can be seen from Figure 7, compare ratio 1, the corrosion resistance nature of the Zr-1Nb-0.01Cu alloy that embodiment 1 is prepared improves 25%.
As can be seen from Figure 8, compare ratio 2, the corrosion resistance nature of the Zr-1Nb-0.01Cu alloy that embodiment 2 is prepared improves 28%.
As can be seen from Figure 9, compare ratio 3, the corrosion resistance nature of the Zr-1.1Nb-0.05Cu alloy that embodiment 3 is prepared improves more than 25%.
From above-mentioned comparing result, compare traditional technology, adopt preparation method of the present invention, the corrosion resistance nature of zirconium alloy is greatly enhanced, and improves more than 25%.
Preparation method of the present invention is applicable to the preparation of Zr-(0.6-1.2) Nb-(0.01-0.1) Cu system alloy.
Above to invention has been detailed description; its object is to allow the personage being familiar with this art can understand content of the present invention and be implemented; can not limit the scope of the invention with this; and the invention is not restricted to the embodiments described; the equivalence change that all spirit according to the present invention are done or modification, all should be encompassed within protection scope of the present invention.

Claims (8)

1. a preparation method for Zr-Nb-Cu system alloy, described preparation method comprises the following steps:
(1) forge: the zirconium alloy product containing Nb and Cu element is forged at 800 ~ 900 DEG C;
(2) quench: quench after the product after step (1) being forged is incubated 20 ~ 40min at 1000 ~ 1050 DEG C;
(3) hot extrusion: the product after step (2) being quenched carries out hot extrusion at 550 ~ 600 DEG C;
(4) anneal first: the product after step (3) hot extrusion is annealed at 500 ~ 550 DEG C;
(5) three cold rolling and annealing: the product after step (4) being annealed first carries out three cold rolling and annealing again, obtained Zr-Nb-Cu system alloy;
It is characterized in that:
In step (5), described three concrete steps that are cold rolling and annealing are as follows:
First time is cold rolling and anneal: it is cold rolling that the product after described step (4) being annealed first carries out first time, after deflection reaches 50 ~ 70%, at 500 ~ 550 DEG C, carries out anneal;
Cold rolling and the annealing of second time: the product after cold rolling for first time and annealing is carried out second time cold rolling, after deflection reaches 50 ~ 70%, carry out anneal at 500 ~ 550 DEG C;
Third time cold rolling and annealing: the product after cold rolling for second time and annealing is carried out third time cold rolling, after deflection reaches 50 ~ 70%, carry out anneal at 450 ~ 520 DEG C.
2. the preparation method of Zr-Nb-Cu system according to claim 1 alloy, is characterized in that: described first time, cold rolling and in annealing annealing time was 0.5 ~ 1.5 hour.
3. the preparation method of Zr-Nb-Cu system according to claim 1 alloy, is characterized in that: cold rolling and in annealing the annealing time of described second time is 0.5 ~ 1.5 hour.
4. the preparation method of Zr-Nb-Cu system according to claim 1 alloy, is characterized in that: described third time, cold rolling and in annealing annealing time was 1.5 ~ 4 hours.
5. the preparation method of Zr-Nb-Cu system according to claim 1 alloy, is characterized in that: described annealing time is first 2 ~ 4 hours.
6. the preparation method of Zr-Nb-Cu system according to claim 1 alloy, is characterized in that: described Zr-Nb-Cu system alloy is that Zr and inevitable impurity form by Nb 0.6-1.2wt.%, Cu 0.01-0.1wt.%, surplus.
7. the preparation method of Zr-Nb-Cu system according to claim 1 alloy, is characterized in that: described Zr-Nb-Cu system alloy is Zr-1Nb-0.01Cu alloy or Zr-1.1Nb-0.05Cu alloy.
8. the preparation method of Zr-Nb-Cu system according to claim 1 alloy, is characterized in that: described Zr-Nb-Cu system second phase particles in alloy is small and dispersed distribution.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109692880A (en) * 2018-12-19 2019-04-30 西部超导材料科技股份有限公司 A kind of Zr-Nb alloy bar material and its extruding method
CN111842486A (en) * 2020-06-24 2020-10-30 江苏圣珀新材料科技有限公司 Cold rolling process of high-temperature alloy GH4169
CN112458337A (en) * 2020-04-13 2021-03-09 国核锆铪理化检测有限公司 Zirconium alloy, preparation method of zirconium alloy and zirconium alloy section
CN112481522A (en) * 2020-04-13 2021-03-12 国核锆铪理化检测有限公司 Zirconium alloy, preparation method of zirconium alloy and zirconium alloy section
CN113355619A (en) * 2021-06-04 2021-09-07 西安交通大学 Heat treatment method for preventing thermal mechanical processing cracking of zirconium alloy

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59226158A (en) * 1983-06-06 1984-12-19 Hitachi Ltd Manufacture of fuel structural member with high corrosion resistance
JPH02250947A (en) * 1989-03-23 1990-10-08 Nippon Nuclear Fuel Dev Co Ltd Corrosion-resistant zirconium-base alloy
CN103650659B (en) * 2005-12-27 2010-03-10 西北有色金属研究院 A kind of preparation method of used by nuclear reactor zirconium-base alloy sheet material
CN102181749A (en) * 2011-06-02 2011-09-14 苏州热工研究院有限公司 Zirconium alloy for nuclear pressurized water reactor and preparation method thereof
CN103194650A (en) * 2013-04-10 2013-07-10 苏州热工研究院有限公司 Preparation method of Zr-1Nb alloy

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59226158A (en) * 1983-06-06 1984-12-19 Hitachi Ltd Manufacture of fuel structural member with high corrosion resistance
JPH02250947A (en) * 1989-03-23 1990-10-08 Nippon Nuclear Fuel Dev Co Ltd Corrosion-resistant zirconium-base alloy
CN103650659B (en) * 2005-12-27 2010-03-10 西北有色金属研究院 A kind of preparation method of used by nuclear reactor zirconium-base alloy sheet material
CN102181749A (en) * 2011-06-02 2011-09-14 苏州热工研究院有限公司 Zirconium alloy for nuclear pressurized water reactor and preparation method thereof
CN103194650A (en) * 2013-04-10 2013-07-10 苏州热工研究院有限公司 Preparation method of Zr-1Nb alloy

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109692880A (en) * 2018-12-19 2019-04-30 西部超导材料科技股份有限公司 A kind of Zr-Nb alloy bar material and its extruding method
CN112458337A (en) * 2020-04-13 2021-03-09 国核锆铪理化检测有限公司 Zirconium alloy, preparation method of zirconium alloy and zirconium alloy section
CN112481522A (en) * 2020-04-13 2021-03-12 国核锆铪理化检测有限公司 Zirconium alloy, preparation method of zirconium alloy and zirconium alloy section
CN112458337B (en) * 2020-04-13 2022-02-18 国核宝钛锆业股份公司 Zirconium alloy and preparation method of zirconium alloy profile
CN111842486A (en) * 2020-06-24 2020-10-30 江苏圣珀新材料科技有限公司 Cold rolling process of high-temperature alloy GH4169
CN113355619A (en) * 2021-06-04 2021-09-07 西安交通大学 Heat treatment method for preventing thermal mechanical processing cracking of zirconium alloy

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