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JPH0528797B2 - - Google Patents

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Publication number
JPH0528797B2
JPH0528797B2 JP61017975A JP1797586A JPH0528797B2 JP H0528797 B2 JPH0528797 B2 JP H0528797B2 JP 61017975 A JP61017975 A JP 61017975A JP 1797586 A JP1797586 A JP 1797586A JP H0528797 B2 JPH0528797 B2 JP H0528797B2
Authority
JP
Japan
Prior art keywords
nuclear fuel
cladding tube
ppm
cladding
weight
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.)
Expired - Lifetime
Application number
JP61017975A
Other languages
Japanese (ja)
Other versions
JPS62194490A (en
Inventor
Masafumi Nakatsuka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Nuclear Fuel Development Co Ltd
Original Assignee
Nippon Nuclear Fuel Development Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Nuclear Fuel Development Co Ltd filed Critical Nippon Nuclear Fuel Development Co Ltd
Priority to JP61017975A priority Critical patent/JPS62194490A/en
Publication of JPS62194490A publication Critical patent/JPS62194490A/en
Publication of JPH0528797B2 publication Critical patent/JPH0528797B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/30Nuclear fission reactors

Landscapes

  • Glass Compositions (AREA)
  • Catalysts (AREA)
  • Monitoring And Testing Of Nuclear Reactors (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔発明の利用分野〕 本発明は核燃料要素に関するものである。 〔発明の背景〕 核燃料要素の被覆管構成材料の元素に関しては
ASTM規格、ASTMB353−77aが知られている。 一般に、核燃料要素は被覆管内に複数個の核燃
料ペレツトが積層収納されると共に、被覆管の両
端開口が端栓により密閉されている。核燃料ペレ
ツトは核分裂性の酸化物燃料粉末を、例えば長さ
と直径との比が約1の円柱状ペレツトに成形焼結
されたものである。また、このように構成された
核燃料要素の被覆管には、核燃料ペレツトとの間
で冷却材が接触することおよび化学反応が生じる
ことを阻止する機能と、燃料から放出された放射
性核分裂生成物が冷却材中に侵入するのを阻止す
る機能とが要求されている。従つてこのような機
能を満足しない被覆管、すなわち被覆管が破損し
たような場合には、冷却系プラントの放射能レベ
ルが上昇し、安全を確保するために原子炉の運転
を停止しなければならなくなる。 一方、水冷型原子炉に用いられる核燃料要素の
被覆管は、一般にジルコニウムおよびそれらの合
金系材料で形成されている。ジルコニウムおよび
その合金は中性子吸収断面積が小さく、かつ約
400℃以下の温度で強靭で延性がよく、冷却材と
して用いられる水蒸気とも反応しない特性を有し
ている。 しかし乍ら現在までの運転経験によると、ジル
コニウムおよびその合金で形成された被覆管で
も、中性子照射を受けることによる材料強度の低
下および核分裂生成物との化学反応による腐食な
どの相互作用に基づく脆性割れが発生している。
このような望ましくない現象は次のようにして発
生するものと考えられる。 すなわち核燃料ペレツトで発生した熱を被覆管
の外表面に効率よく伝えるには、被覆管の内側面
と核燃料ペレツトとの間に形成されるギヤツプを
数十ミクロン以下に設定する必要がある。一方、
運転時には核燃料ペレツトが発熱するので、ペレ
ツト自身が熱応力で割れてその破面の喰い違い
や、さらには燃焼と共に核燃料ペレツト内に核分
裂生成物が累積して起こる体積膨張などが原因し
て、被覆管が核燃料ペレツトによつて押し拡げら
れ応力を受ける。被覆管が受ける歪の円周方向の
平均値はさほど大きくはないが、核燃料ペレツト
に生じたクラツク近傍の壁には局部的に歪が集中
するのみならず、この歪は降伏応力以上に達す
る。さらに、核分裂に伴なつて核燃料ペレツトか
らヨウ素およびヨウ素化合物、セシウムおよびセ
シウム化合物などの腐食性ガスが発生し、この腐
食性ガスは被覆管内の自由空間、すなわちクラツ
クなどに集まる。とりわけ被覆管の特に歪が集中
している部分近傍に腐食性ガスが集まり易い。 一般に、腐食性ガスの雰囲気中で応力(特に降
伏応力以上)が作用すると、材料の延性が低減
し、応力腐食割れと称される脆性破壊現象が発生
する。応力腐食割れは温度、応力、腐食性ガスの
濃度、溶存酸素、合金の組成、熱処理、加工度な
どによつても左右され、その発生メカニズムは単
一ではない。これらの望ましくない破壊を防止す
る目的で被覆管を内張りする概念は周知であり、
米国特許3502549号公報、米国特許3625821号公
報、特開昭51−69792号公報、特開昭51−69795号
公報、特開昭51−69796号公報および特開昭51−
71497号公報において、ライナー材としてMo、
W、Nb、Ni、Fe、Mg、Cu、純Zr、Al、Ni−
Cr合金、アルミ化コーテング、珪素化コーテン
グ等が示されている。 しかし乍らこのような障壁材としてのライナー
材のあるものは、中性子吸収断面積が大きく炉の
経済性を低下させるなどの欠点がある。また、ラ
イナー材を用いると被覆管の製造工程が増すだけ
でなく、固有の技術的問題および経済的不利を生
じる問題があつた。 〔発明の目的〕 本発明は以上の点に鑑みなされたものであり、
耐応力腐食割れ性能を増大し、信頼性、経済性を
向上することを可能とした核燃料要素を提供する
ことを目的とするものである。 〔発明の概要〕 すなわち本発明は被覆管の内部に核燃料ペレツ
トが密封されている核燃料要素において、前記被
覆管が炭素濃度80重量ppm以下で、かつ酸素濃度
600重量ppm以下のジルコニウム合金から形成さ
れたものであることを特徴とするものであり、こ
れによつて被覆管の応力腐食割れが起こり難くな
る。 発明者はどのようにすれば耐応力腐食割れ性が
向上できるかを検討した。ジルコニウム合金を構
成する元素のうち、高温(約350℃)における強
度を増加させるのはジルコニウム中に固溶する主
として酸素などの元素である。この他に結晶粒内
に分散し、被覆管の強度を増加させる主要な元素
に炭素がある。従来、炭素は約140重量ppm程度
含まれているが、この濃度をさらに低下させるこ
とは工業的に可能である。また、従来酸素濃度は
被覆管の使用初期の強度を確保するための約1100
から1300重量ppmに定めていたが、本発明では被
覆管の高温強度を低く押えるためには炭素と共に
酸素の濃度を制限すれば、燃料と被覆管との相互
作用に起因する応力腐食割れに対してすぐれた被
覆管が得られる点に着目した。 〔発明の実施例〕 第1表には本発明の実施例で用いるジルコニウ
ム合金のジルコニウムを除いた化学組成が示して
あり、イ、ロ、ハ、ニのうちハ、ニは従来例、
イ、ロは実施例である。まず、原子炉級ジルカロ
イ−2の化学組成規格(ASTM、B−353、
Grade、RA−1)を満足する次の量の合金元素
をジルコニウム中に添加する。すなわち錫1.20か
ら1.70重量%、鉄0.07から0.20重量%、クロム
0.05から0.15重量%、ニツケル0.03から0.08重量
%、鉄+クロム+ニツケル0.18から0.38重量%で
ある。次に従来の上記規格では炭素は270重量
ppm以下であるが、実施例イ、ロは炭素濃度が
夫々50、80重量ppm、酸素濃度が夫々400、600重
量ppmとし、他の不純物元素は上記規格を満足す
るようなジルコニウムインゴツトとした。従来例
ハ、ニは炭素濃度が夫々140、170重量ppm、酸素
濃度が夫々1100、1300重量ppmと上述のように従
来の炭素濃度約140重量ppm、酸素濃度約1100か
ら1300重量ppmを満足するインゴツトとした。
FIELD OF APPLICATION OF THE INVENTION The present invention relates to nuclear fuel elements. [Background of the Invention] Regarding the elements of the cladding material of nuclear fuel elements,
The ASTM standard ASTMB353-77a is known. Generally, in a nuclear fuel element, a plurality of nuclear fuel pellets are stacked and stored in a cladding tube, and both openings of the cladding tube are sealed with end plugs. Nuclear fuel pellets are formed by forming and sintering fissile oxide fuel powder into cylindrical pellets having, for example, a length to diameter ratio of about 1. In addition, the cladding tube of a nuclear fuel element configured in this manner has the function of preventing the coolant from coming into contact with the nuclear fuel pellets and preventing chemical reactions from occurring, and the function of preventing radioactive fission products released from the fuel. A function is required to prevent coolant from entering the coolant. Therefore, in the event that the cladding tube does not satisfy these functions, that is, the cladding tube is damaged, the radioactivity level in the cooling system plant will increase, and reactor operation must be stopped to ensure safety. It will stop happening. On the other hand, cladding tubes of nuclear fuel elements used in water-cooled nuclear reactors are generally made of zirconium and alloys thereof. Zirconium and its alloys have a small neutron absorption cross section and approximately
It is strong and ductile at temperatures below 400°C, and has the property of not reacting with water vapor, which is used as a coolant. However, according to operational experience to date, even cladding tubes made of zirconium and its alloys are susceptible to brittleness due to a decrease in material strength due to neutron irradiation and corrosion due to chemical reactions with nuclear fission products. Cracks have occurred.
It is thought that such an undesirable phenomenon occurs as follows. That is, in order to efficiently transfer the heat generated by the nuclear fuel pellet to the outer surface of the cladding tube, it is necessary to set the gap formed between the inner surface of the cladding tube and the nuclear fuel pellet to several tens of microns or less. on the other hand,
During operation, nuclear fuel pellets generate heat, so the pellets themselves crack due to thermal stress, resulting in discrepancies in the fracture surfaces, and furthermore, fission products accumulate within the nuclear fuel pellets as they burn, resulting in volumetric expansion. The tube is expanded and stressed by the nuclear fuel pellets. Although the average value of the strain to which the cladding tube is subjected in the circumferential direction is not very large, the strain is not only locally concentrated on the wall near the crack that occurs in the nuclear fuel pellet, but this strain reaches more than the yield stress. Further, as nuclear fission occurs, corrosive gases such as iodine and iodine compounds, cesium and cesium compounds are generated from nuclear fuel pellets, and these corrosive gases collect in free spaces within the cladding tube, such as cracks. In particular, corrosive gas tends to collect near parts of the cladding where strain is particularly concentrated. Generally, when stress (particularly greater than yield stress) is applied in a corrosive gas atmosphere, the ductility of the material decreases and a brittle fracture phenomenon called stress corrosion cracking occurs. Stress corrosion cracking is also affected by temperature, stress, concentration of corrosive gas, dissolved oxygen, alloy composition, heat treatment, degree of processing, etc., and the mechanism by which it occurs is not unique. The concept of lining cladding pipes to prevent these undesirable fractures is well known;
U.S. Pat. No. 3,502,549, U.S. Pat. No. 3,625,821, JP-A-51-69792, JP-A-51-69795, JP-A-51-69796, and JP-A-Sho. 51-
In Publication No. 71497, Mo as a liner material,
W, Nb, Ni, Fe, Mg, Cu, pure Zr, Al, Ni−
Cr alloys, aluminized coatings, silicided coatings, etc. are shown. However, some liner materials used as barrier materials have drawbacks such as a large neutron absorption cross section, which reduces the economic efficiency of the reactor. Additionally, the use of liner materials not only increases the manufacturing process of the cladding, but also presents inherent technical problems and economic disadvantages. [Object of the invention] The present invention has been made in view of the above points,
The object of the present invention is to provide a nuclear fuel element that has increased stress corrosion cracking resistance and improved reliability and economic efficiency. [Summary of the Invention] That is, the present invention provides a nuclear fuel element in which nuclear fuel pellets are sealed inside a cladding tube, in which the cladding tube has a carbon concentration of 80 ppm or less and an oxygen concentration of 80 ppm or less.
It is characterized by being formed from a zirconium alloy of 600 ppm or less by weight, which makes stress corrosion cracking of the cladding less likely to occur. The inventor investigated how stress corrosion cracking resistance could be improved. Among the elements constituting the zirconium alloy, the elements that increase the strength at high temperatures (approximately 350°C) are mainly elements such as oxygen, which are dissolved in zirconium. In addition, carbon is a major element that is dispersed within the crystal grains and increases the strength of the cladding. Conventionally, carbon is contained at about 140 ppm by weight, but it is industrially possible to further reduce this concentration. In addition, the conventional oxygen concentration was approximately 1100 to ensure the initial strength of the cladding tube.
However, in the present invention, in order to keep the high temperature strength of the cladding tube low, limiting the concentration of oxygen as well as carbon will prevent stress corrosion cracking caused by the interaction between the fuel and the cladding tube. We focused our attention on the fact that an excellent cladding tube could be obtained. [Embodiments of the Invention] Table 1 shows the chemical compositions of the zirconium alloys used in the embodiments of the present invention, excluding zirconium.
A and B are examples. First, the chemical composition standard (ASTM, B-353,
The following amount of alloying elements satisfying Grade, RA-1) are added to zirconium. i.e. 1.20-1.70% by weight of tin, 0.07-0.20% by weight of iron, chromium
0.05 to 0.15% by weight, 0.03 to 0.08% by weight of nickel, and 0.18 to 0.38% by weight of iron + chromium + nickel. Next, according to the conventional standards mentioned above, carbon weighs 270
ppm or less, but in Examples A and B, the carbon concentration was 50 and 80 ppm by weight, respectively, the oxygen concentration was 400 and 600 ppm by weight, respectively, and the other impurity elements were zirconium ingots that satisfied the above specifications. . Conventional examples C and D have carbon concentrations of 140 and 170 ppm by weight, respectively, and oxygen concentrations of 1100 and 1300 ppm by weight, respectively, satisfying the conventional carbon concentration of about 140 ppm by weight and oxygen concentration of about 1100 to 1300 ppm by weight, as described above. It was made into an ingot.

【表】【table】

〔発明の効果〕〔Effect of the invention〕

上述のように本発明は耐応力腐食割れ性能が増
大し、信頼性、経済性が向上するようになつて、
耐応力腐食割れ性能を増大し、信頼性、経済性を
向上することを可能とした核燃料要素を得ること
ができる。
As mentioned above, the present invention has increased stress corrosion cracking resistance, improved reliability and economical efficiency,
It is possible to obtain a nuclear fuel element with increased stress corrosion cracking resistance and improved reliability and economic efficiency.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の核燃料要素の一実施例の被覆
管製造工程図、第2図は同じく一実施例の製造し
た被覆管の円周方向破断伸び特性図である。
FIG. 1 is a process diagram for manufacturing a cladding tube according to one embodiment of the nuclear fuel element of the present invention, and FIG. 2 is a diagram showing the elongation at break in the circumferential direction of the cladding tube manufactured according to the same embodiment.

Claims (1)

【特許請求の範囲】 1 被覆管の内部に核燃料ペレツトが密封されて
いる核燃料要素において、前記被覆管が炭素濃度
80重量ppm以下で、かつ酸素濃度600重量ppm以
下のジルコニウム合金から形成されたものである
ことを特徴とする核燃料要素。 2 前記ジルコニウム合金が、ジルカロイから形
成されたものである特許請求の範囲第1項記載の
核燃料要素。
[Scope of Claims] 1. A nuclear fuel element in which nuclear fuel pellets are sealed inside a cladding tube, wherein the cladding tube has a carbon concentration
A nuclear fuel element characterized in that it is formed from a zirconium alloy with an oxygen concentration of 80 ppm or less and an oxygen concentration of 600 ppm or less. 2. The nuclear fuel element of claim 1, wherein the zirconium alloy is formed from Zircaloy.
JP61017975A 1986-01-31 1986-01-31 Nuclear fuel element Granted JPS62194490A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61017975A JPS62194490A (en) 1986-01-31 1986-01-31 Nuclear fuel element

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61017975A JPS62194490A (en) 1986-01-31 1986-01-31 Nuclear fuel element

Publications (2)

Publication Number Publication Date
JPS62194490A JPS62194490A (en) 1987-08-26
JPH0528797B2 true JPH0528797B2 (en) 1993-04-27

Family

ID=11958726

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61017975A Granted JPS62194490A (en) 1986-01-31 1986-01-31 Nuclear fuel element

Country Status (1)

Country Link
JP (1) JPS62194490A (en)

Also Published As

Publication number Publication date
JPS62194490A (en) 1987-08-26

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