Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS608474B2 - Method for measuring burnup of fuel assembly - Google Patents
[go: Go Back, main page]

JPS608474B2 - Method for measuring burnup of fuel assembly - Google Patents

Method for measuring burnup of fuel assembly

Info

Publication number
JPS608474B2
JPS608474B2 JP51127355A JP12735576A JPS608474B2 JP S608474 B2 JPS608474 B2 JP S608474B2 JP 51127355 A JP51127355 A JP 51127355A JP 12735576 A JP12735576 A JP 12735576A JP S608474 B2 JPS608474 B2 JP S608474B2
Authority
JP
Japan
Prior art keywords
neutron
fuel assembly
fuel
burnup
neutrons
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
Application number
JP51127355A
Other languages
Japanese (ja)
Other versions
JPS5352894A (en
Inventor
精 植田
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.)
Toshiba Corp
Nippon Genshiryoku Jigyo KK
Original Assignee
Toshiba Corp
Nippon Genshiryoku Jigyo KK
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 Toshiba Corp, Nippon Genshiryoku Jigyo KK filed Critical Toshiba Corp
Priority to JP51127355A priority Critical patent/JPS608474B2/en
Publication of JPS5352894A publication Critical patent/JPS5352894A/en
Publication of JPS608474B2 publication Critical patent/JPS608474B2/en
Expired 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

  • Monitoring And Testing Of Nuclear Reactors (AREA)

Description

【発明の詳細な説明】 本発明は燃料集合体の燃焼度を測定する方法に関し、さ
らに詳しくは照射燃料から放出される中性子を利用する
燃焼度の測定方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for measuring burnup of a fuel assembly, and more particularly to a method for measuring burnup using neutrons emitted from irradiated fuel.

燃料集合体が原子炉に装荷されてから燃焼することによ
り、どれだけの熱エネルギーが当該燃料から取出された
かを表わす尺度を燃料集合体の燃焼度とよぶ。燃料集合
体は原子炉に装荷されて中性子の照射を受け照射燃料と
なるが、照射燃料中には中性子を放出する超ウラン元素
が生成される。照射燃料から放出される中性子を利用し
た燃焼度の測定方法を列挙すると次の通りである。
The burnup of a fuel assembly is a measure of how much thermal energy is extracted from the fuel when the fuel assembly is loaded into a nuclear reactor and burned. The fuel assembly is loaded into a nuclear reactor and irradiated with neutrons to become irradiated fuel, and transuranic elements that emit neutrons are generated in the irradiated fuel. The burnup measurement methods using neutrons emitted from irradiated fuel are listed below.

(11 燃焼度と中性子発生数との関係を利用する方法
。‘21 強度既知の外部中性子源を利用して中性子発
生数を求め燃焼度と中性子発生数との関係から求める方
法。
(11 A method that uses the relationship between burnup and the number of neutrons generated. '21 A method that uses an external neutron source of known intensity to determine the number of neutrons generated from the relationship between burnup and the number of neutrons generated.

(3’超ウラン元素Cm−242,Cm−244から放
出される中性子を他の核種から放出される中性子と区別
することにより、両者の比と燃焼度との関係から求める
方法。
(3' A method of determining neutrons emitted from transuranium elements Cm-242 and Cm-244 from the relationship between the ratio of the two and the burnup by distinguishing them from neutrons emitted from other nuclides.

これら3つの従来の測定方法は核分裂によって生じた中
性子の吸収により生成した超ウラン元素の生成量を測定
することによって間接的に燃焼度を求めているから間接
的な方法ということができる。
These three conventional measurement methods can be called indirect methods because they indirectly determine the burnup by measuring the amount of transuranium elements produced by absorption of neutrons generated by nuclear fission.

本発明の目的は前述の間接的な方法と異なり、直接的方
法というべきもので、燃料集合体の内部または周囲に形
成される中性子スペクトル中性子東比の形で測定するこ
とによって燃料集合体の燃焼度を測定する方法を提供す
るにある。
The object of the present invention is different from the above-mentioned indirect method, and is a direct method, in which the combustion of a fuel assembly is determined by measuring the neutron spectrum formed in or around the fuel assembly in the form of neutron ratio. To provide a method to measure the degree of

以下本発明の原理を数式を用いて詳細に説明する。The principle of the present invention will be explained in detail below using mathematical formulas.

まず軽水のような中性子減速材と照射燃料とが供存する
体系について、熱中性子炉の理論に用いられる2群拡散
理論により中性子の振舞を表せば次式が得られる。すな
わち(2岬十ZsdF+DFBF2)○F;(し2f)
F◇F+(し2f)TOT+S【11(2aT+DTB
T2 )○T=2sdF◇F 【21ここにS=
中性子発生源強度 F=高速中性子群に対する指標 T=熱中性子群に対する指標 Zが,ZaT;F、T群の吸収断面積 23dF=F群の減速断面積 ○F,DT=F,T群の拡散係数 BF2,Bで=F,T群のバックリング 中F,07=F,T群の中性子東(少Fを高速中性子東
、?Tを熱中性子東とよぶ) (リ2f)F?F,(し2f)TOT=F,T群の中性
子による中性子発生率(この中性子発生率は当該体系に
中 性子発生源Sがあって形成する中性 子東に基づいて誘発核分裂が生ずる 場合の中性子発生率であって、? F,?Tは共に中性子発生源と誘発核 分裂によって構成される。
First, for a system in which a neutron moderator such as light water and irradiated fuel exist, the following equation can be obtained by expressing the behavior of neutrons using the two-group diffusion theory used in the theory of thermal neutron reactors. That is, (2 Cape 10 ZsdF + DFBF2)○F; (2f)
F◇F+(shi2f)TOT+S[11(2aT+DTB
T2 )○T=2sdF◇F [21 here S=
Neutron source strength F = Index for fast neutron group T = Index for thermal neutron group Z is ZaT; Absorption cross section of F, T group 23 dF = Deceleration cross section of F group ○ F, DT = Diffusion of F, T group With coefficient BF2, B = F, during buckling of T group F, 07 = F, neutron east of T group (small F is called fast neutron east, ?T is called thermal neutron east) (Li2f) F? F, (2f) TOT = neutron generation rate by neutrons of F, T group (this neutron generation rate is the neutron generation rate when there is a neutron source S in the system and induced fission occurs based on the neutron east formed Both ?F and ?T are composed of a neutron source and induced nuclear fission.

)‘2ー式から次の‘3’式が得られる ◇F/OT:(2aT+DTBT2 )/2SdF=(
ZaT/2sdF)(1十L2&2) ■ここに
び=DT/2aT=熱中性子拡散面積L虫T2の値は一
般に1に比べてかなりあるいは非常に小さいので?P/
ぐTに対するL沼T2の影響は4・さし・。
) The following '3' formula can be obtained from the '2-equation ◇F/OT: (2aT+DTBT2 )/2SdF=(
ZaT/2sdF) (10L2&2) ■Kokobi = DT/2aT = Thermal neutron diffusion area L Since the value of T2 is generally considerably or very small compared to 1? P/
The influence of L Swamp T2 on GuT is 4.

従って理論計算などで別に求めてもぐF/JTの値につ
いては誤差の原因とはならない。本発明の原理は【3}
式に基づくものである。
Therefore, the value of F/JT obtained separately by theoretical calculation etc. will not be a cause of error. The principle of the present invention is [3]
It is based on the formula.

すなわち核分裂が進む(燃焼が進む)に従って熱中性吸
収断面積の特に大きなU−235やPu−239などの
ような核分裂性核種の量が減損して行くため、2aTの
値は次第に減少する。この現象をさらに詳しく次に説明
する。燃料としてウランを用いる場合を考えると、燃焼
が進むにつれてU−235が減損し、Pu−239,P
u−240,Pu−241などの核分裂性の核種や核分
裂片が生成する。U−235の減損は2aTを小さくす
るが、Pu−240,Pu−241、核分裂片等の生成
は逆に28丁を大きくする。Pu−240の生成はさら
に2sdFの値を僅かであるが減少させる。これらのこ
とを考えるとJF/OTの値は燃焼の進行に伴なつて増
大するのか減少するのかかからないが、軽水炉燃料など
転換比が1よりある程度小さいもの、すなわち燃焼に従
ってU−235の減損がPu−239などの生成より速
やかに進行する場合には、2aTは減少効果の方が勝り
、?F/?Tの値は減少する。核分裂片の吸収断面積は
Xe−135を除いては小さく、Xe−135は半減期
が短いので原子炉停止後10日もたつと消滅してしまう
。このため原子炉停止後10日もたつと、2aTの増大
に寄与する核分裂片の生成の効果は小さい。Pu−24
0が生成すると2sdpの値は僅かではあるが減少する
ので、結局SaTと2sdFの減少の速やかさの違いに
よってめF/◇Tの値が減少するか増大するかが決まる
。U−235の濃縮度が高くなると、燃焼に伴なつてU
−235の減損がPu−239などの生成よりはるかに
早く進行するため、?F/?Tの値は減少する。プルト
ニウムをウランの中に富化した燃料では、U−2粉から
のPu一239の生成より最初から富化されていたPu
−239の減損の方が燃焼に伴なつて早く進行するため
、JF/◇Tの値は減少することが多いが、Pu−24
0のプルトニウム中に占める割合が特に大きい場合、必
ずしもぐF/JTの値は減少するとは限らない。転換比
が1より大きいといわれる高速増殖炉の場合は、炉心部
が濃縮度の高いウランや富化度の高いプルトニウムが用
いられ「プランケツト部には減損ウランなどが用いられ
る。高速増殖炉で転換比が1より大きい、すなわち燃焼
に伴なつて核分裂性核種が増殖されるというのは、炉心
とプランケツトを一括して考えた場合であって、炉心部
ではU−235やPu一239などの核分裂性核種が減
損し、プランケット部ではPu−239が増大する。従
って炉心部の燃料に着目してOF/OTの測定を行なえ
ば、この値は減少し、プランケツト部の燃料の場合は逆
に増大する。次に沸騰水型原子炉(以下BWRと略す。
That is, as nuclear fission progresses (combustion progresses), the amount of fissile nuclides such as U-235 and Pu-239, which have particularly large thermal neutral absorption cross sections, is depleted, so the value of 2aT gradually decreases. This phenomenon will be explained in more detail below. Considering the case where uranium is used as fuel, as combustion progresses, U-235 is depleted and Pu-239, P
Fissile nuclides and fission fragments such as u-240 and Pu-241 are generated. Depletion of U-235 reduces 2aT, but production of Pu-240, Pu-241, fission fragments, etc. conversely increases 28 guns. The production of Pu-240 further reduces the value of 2sdF, albeit slightly. Taking these things into consideration, the value of JF/OT does not matter whether it increases or decreases as combustion progresses, but it does not matter whether the value of JF/OT increases or decreases as combustion progresses. If it progresses more quickly than the production of -239 etc., the reduction effect of 2aT is superior, and? F/? The value of T decreases. The absorption cross section of fission fragments is small except for Xe-135, and Xe-135 has a short half-life, so it disappears 10 days after the reactor is shut down. For this reason, 10 days after the nuclear reactor is shut down, the effect of the production of fission fragments that contributes to an increase in 2aT is small. Pu-24
When 0 is generated, the value of 2sdp decreases, albeit slightly, so whether the value of F/◇T decreases or increases is ultimately determined by the difference in the speed of decrease of SaT and 2sdF. As the enrichment of U-235 increases, U-235 increases as it burns.
Because the depletion of -235 proceeds much faster than the production of Pu-239 etc.? F/? The value of T decreases. In the fuel enriched with plutonium in uranium, the Pu-239 that was enriched from the beginning was generated from the U-2 powder.
Since the depletion of -239 progresses faster with combustion, the value of JF/◇T often decreases, but the value of Pu-24
If the proportion of 0 in plutonium is particularly large, the value of F/JT does not necessarily decrease. In the case of fast breeder reactors whose conversion ratio is said to be greater than 1, highly enriched uranium or highly enriched plutonium is used for the reactor core, and depleted uranium is used for the plunger part. The fact that the conversion ratio is greater than 1, that is, that fissile nuclides are multiplied during combustion, is when considering the reactor core and the plunket as a whole. fissile nuclides are depleted, and Pu-239 increases in the plunket part.Therefore, if OF/OT is measured focusing on the fuel in the reactor core, this value will decrease; On the contrary, it increases.Next is the boiling water reactor (hereinafter abbreviated as BWR).

)の標準的な燃料集合体(平均濃度2.5%のウラン燃
料)を燃焼させた場合について定量的に説明する。第1
図は前記のBWR燃料集合体の燃焼度と中性子東比との
関係を示す校正曲線の図である。
We will quantitatively explain the case where a standard fuel assembly (uranium fuel with an average concentration of 2.5%) is burned. 1st
The figure is a diagram of a calibration curve showing the relationship between the burnup of the BWR fuel assembly and the neutron east ratio.

この校正曲線の作成には相対変化を計算で求め、絶対値
は新燃料など燃焼度既知の燃料集合体を用いて測定する
のが便利である。図において(ZaT/23dF)の値
(相対値で示す)はほぼ直線的に減少しているが、20
〜3鷹Wd/t以上の燃焼度で曲線1の減少はゆるやか
になっている。その主な原因はPu−240とPu−2
41の生成により2aTの減少が抑制されるためである
。実際に達成される燃焼度はこの計算例に用いた燃料集
合体の場合せいぜい3のWd/t程度であるため曲線1
の曲がり2の補正は理論計算で行なうことができる。本
例より大きな燃焼度をうるよう設計された燃料集合体で
はU−235などの濃縮度は2.5%より大きくされる
。濃縮度が高くなれば曲線の曲り2は高燃焼度の側にず
れるので、前記のような曲りの補正は前記例と同機に理
論計算で行なうことができる。濃縮度が2〜2.5%程
度の場合は曲り2は低燃焼度の側にずれるが、そのよう
な燃焼の場合は達成できる燃焼度の最高値も低下するの
で曲りの補正はやはり同様に行なうことができる。濃縮
度が1.5%程度以下の燃料を濃縮度が比較的高い燃料
と一緒に原子炉に装荷して比較的高い燃焼度を得ようと
する場合には、U−235の減損に伴なうSaTの減少
効果とPu−239,Pu−240,Pu−241など
の生成に伴なうZ幻の増大効果とが相殺し合い、OF/
ふの変化が複雑かつ小さくなるので、‘3’式の原理を
そのまま適用できない。
To create this calibration curve, it is convenient to calculate the relative change and measure the absolute value using a fuel assembly with known burnup, such as new fuel. In the figure, the value of (ZaT/23dF) (shown as a relative value) decreases almost linearly, but when 20
The decrease in curve 1 becomes gradual at burn-up of ~3 Wd/t or higher. The main causes are Pu-240 and Pu-2
This is because the production of 41 suppresses the decrease in 2aT. The burnup actually achieved is at most about 3 Wd/t for the fuel assembly used in this calculation example, so the curve 1
Correction of the curve 2 can be performed by theoretical calculation. In a fuel assembly designed to obtain a higher burnup than this example, the enrichment of U-235 or the like is set to be greater than 2.5%. Since the curve 2 of the curve shifts to the high burnup side as the enrichment level increases, the above-mentioned curve correction can be performed by theoretical calculation for the same aircraft as in the above example. When the enrichment is about 2 to 2.5%, bend 2 shifts to the low burnup side, but in such a combustion case, the maximum burnup that can be achieved also decreases, so the correction for the bend is still the same. can be done. When attempting to obtain a relatively high burnup by loading fuel with an enrichment of about 1.5% or less into a reactor together with fuel with a relatively high enrichment, the OF/
Since the change in pressure becomes complex and small, the principle of the '3' formula cannot be applied as is.

このような場合にはエネルギーが鉾V以下の中性子だけ
に着目し「中性子スペクトルと燃焼度との関係を利用し
て中性子スペクトルに関する測定値から燃焼度を求める
のがよい。中性子検出器としてはたとえばデイスプロシ
ウム(Dy)とPu一般9の箔を燃料集合体の内部に挿
入して熱中性子により放射化すると、燃料が進んだ燃料
では、燃料の中にPu−239などが生成しているため
、0.$V近傍の中性子を多く吸収して0。$V付近の
中性子東が低下するが、〜0.1eV以下の中性子はあ
まり吸収しないため、中性子検出器のPu−23$管と
DX箔との反応率の比は燃焼が進むにつれて減小する。
Pu−239の箔は比較的エネルギーの高い熱中性子(
0.1〜0.&V付近)に感じ易く、Dyは比較的エネ
ルギーの低い熱中性子(約0.1eV以下)に感じ易い
。従って前記Pu−23群筈とDX箔との反応率の比は
比較的エネルギーの高い熱中性子東と低いそれとの比と
みなすことができる。熱中性子の範囲でこのような比を
糊式のように解析的に表現することは困難なため、すで
に高度に開発されている熱中性子多群輸送計算理論に基
づく数値計算コード(たとえばTHERMOSコード)
を用いればよい。前記の説明では中性子検出器としてP
u−239とDyの箔を用いたが、燃料中に生成したP
u−240,Am−241などによる中性子東の低下に
敏感なln,Rhなどの箔をPu−23巽贋の代りに用
いてもよく、あわせて用いてもよい。また箔の状態に限
定しなくてもよい。次にBWR燃料集合体を水プール中
に設置した場合を考える。
In such cases, it is best to focus only on neutrons with energy below Hoko V and use the relationship between the neutron spectrum and burnup to determine the burnup from the measured value of the neutron spectrum.As a neutron detector, for example, When a foil of disprosium (Dy) and Pu general 9 is inserted inside a fuel assembly and activated by thermal neutrons, Pu-239 etc. are generated in the fuel in the advanced fuel. , absorbs many neutrons near 0.$V, and the neutron east near 0.$V decreases, but neutrons below ~0.1eV are not absorbed much, so the Pu-23$ tube of the neutron detector and DX The ratio of reaction rate to foil decreases as combustion progresses.
Pu-239 foil has relatively high energy thermal neutrons (
0.1~0. &V), and Dy tends to be sensitive to relatively low-energy thermal neutrons (approximately 0.1 eV or less). Therefore, the ratio of reaction rates between the Pu-23 group and the DX foil can be regarded as the ratio between thermal neutrons with relatively high energy and those with relatively low energy. Since it is difficult to express such a ratio analytically in the range of thermal neutrons like a glue formula, numerical calculation codes (e.g. THERMOS code) based on the already highly developed thermal neutron multigroup transport calculation theory are used.
You can use In the above explanation, P is used as a neutron detector.
Although U-239 and Dy foils were used, P generated in the fuel
Foils such as ln and Rh, which are sensitive to the decrease in neutron energy due to u-240, Am-241, etc., may be used in place of the Pu-23 foil, or may be used in combination. Moreover, it does not have to be limited to the state of foil. Next, consider the case where the BWR fuel assembly is installed in a water pool.

第2図aにおいて燃料集合体3は多数の核燃料榛4から
なりこれらの燃料棒4がチャンネルボックス5の内部に
収められている。各燃料綾間は水プールの水6で占めら
れており、この水は減速材としての働きをする。チャン
ネルボックス5の外部もプール水7でみたされ、この水
は反射材の働きをする。第2図bは第2図aの矢印A−
Aの方向の中性子東分布を示す図である。図において熱
中性子東◇Tは反射材7の中で大きく盛り上っているが
、これは主として燃料集合体3内から洩れ出した高速中
性子が反射材7で減速されて熱中性子化されるためであ
る。燃料集合体内部に生じた熱中性子が洩れて反射材7
に出てくるのは僅かであるため、反射材中の熱中性子東
はほぼ燃料集合体内部の高速中性子東でFに比例する。
従って反射村内の熱中性子東と燃料集合体内部の熱中性
子東との比は剛式のJF/OTにほぼ比例することがわ
かる。次に反射材7の中で減速されていない高速中性子
東を測定する方法を説明する。
In FIG. 2a, the fuel assembly 3 consists of a large number of nuclear fuel rods 4, and these fuel rods 4 are housed inside a channel box 5. Each fuel twill is occupied by water 6 from a water pool, which acts as a moderator. The outside of the channel box 5 is also filled with pool water 7, and this water acts as a reflective material. Figure 2b is the arrow A- in Figure 2a.
It is a figure which shows the neutron east distribution in the direction of A. In the figure, thermal neutrons East◇T are greatly raised inside the reflector 7, but this is mainly because the fast neutrons leaking from within the fuel assembly 3 are decelerated by the reflector 7 and converted into thermal neutrons. It is. Thermal neutrons generated inside the fuel assembly leak and strike the reflective material 7.
Since only a small amount of thermal neutrons come out in the reflector, the thermal neutrons in the reflector are almost proportional to F in the fast neutrons inside the fuel assembly.
Therefore, it can be seen that the ratio of thermal neutron east within the reflection village to thermal neutron east inside the fuel assembly is approximately proportional to the rigid JF/OT. Next, a method of measuring fast neutrons that are not decelerated in the reflector 7 will be explained.

反射材内の高速中性子東は燃料集合体内部のそれに比例
するため、反射材内の高速中性子東と燃料集合体内の熱
中性子束との比は同様に{3}式の?F/◇Tに比例す
る。次にのべる方法は燃料集合体の側定に鉛、炭素、重
水、空洞等のような熱中性子を導き易い物質(以下熱中
性子誘導体とよぶ)をおき、燃料集合体内部の熱中性子
を集合体外部へ導出することによって熱中性子東を集合
体外部で測定し、一方高速中性子は反射材を構成してい
る水の領域に導き減速させて熱中性子とし、両領域の熱
中性子東の比が【3}式の◇F/?Tの値に比例すると
ころから燃焼度を求めるものである。
Since the fast neutron flux in the reflector is proportional to that inside the fuel assembly, the ratio between the fast neutron flux in the reflector and the thermal neutron flux in the fuel assembly is similarly expressed in equation {3}? F/◇Proportional to T. The next method is to place materials that easily guide thermal neutrons (hereinafter referred to as thermal neutron derivatives) such as lead, carbon, heavy water, cavities, etc. in the fuel assembly, and aggregate thermal neutrons inside the fuel assembly. Thermal neutrons are measured outside the assembly by being guided outside, while fast neutrons are guided into the water region that makes up the reflective material and decelerated to become thermal neutrons, and the ratio of thermal neutrons in both regions is [ 3) ◇F/? The burnup is determined from the value that is proportional to the value of T.

集合体外部で直接高速中性子東を測定してもよく、この
場合前記熱中性子誘導体内で高速中性子東を測定しても
よい。第3図は燃料集合体3の内部または周囲の少なく
とも一方に中性子検出器を装着した実施例であって、図
aは燃料集合体内部の多数の核燃料榛4の中の1本を引
抜き、そこに金箔などの中性子検出器を装着した棒状中
性子検出装置8を取付けた図である。同図bは穣状中性
子検出装置8と8aを取付けた図であって検出装置8a
は燃料集合体3の周辺の反射材7中に設置されている。
同図cも棒状中性子検出装置8と8aを設置した例であ
って装置8は前記熱中性子誘導体9の内部に、装置8a
は反射材7の中に設置されている。第3図a,bおよび
cは前述の方法における中性子検出装置の配置の代表例
である。第4図は停止中のBWR原子炉炉心内に棒状中
性子検出装置8を装着した図である。
Fast neutron east may be measured directly outside the assembly, or in this case fast neutron east may be measured within the thermal neutron derivative. FIG. 3 shows an embodiment in which a neutron detector is installed inside or around at least one of the fuel assemblies 3, and FIG. It is a diagram in which a rod-shaped neutron detection device 8 equipped with a neutron detector such as gold foil is attached. FIG.
are installed in the reflective material 7 around the fuel assembly 3.
FIG.
is installed inside the reflective material 7. Figures 3a, b and c are representative examples of the arrangement of neutron detection devices in the method described above. FIG. 4 is a diagram showing the rod-shaped neutron detection device 8 installed in the core of a BWR nuclear reactor that is stopped.

原子炉停止中十字型制御棒10は炉心に全挿入されてお
り「1本の制御棒は破線11で囲まれた4本の燃料集合
体を支配している。棒状中性子検出装置8は燃料集合体
内に、検出装置8bは燃料集合体外部に設置されている
。炉心からの中性子漏洩がないため第3図aの8の位置
に比して20〜5針部まどの中性子東が得られる。本発
明にかかる方法ほどの型の原子炉の燃料集合体の燃焼度
測定に応用できる。
During reactor shutdown, the cross-shaped control rods 10 are fully inserted into the reactor core, and one control rod controls four fuel assemblies surrounded by broken lines 11. Inside the body, the detection device 8b is installed outside the fuel assembly.Since there is no neutron leakage from the reactor core, neutrons from 20 to 5 needles can be obtained compared to the position 8 in FIG. 3a. The method according to the invention can be applied to burnup measurements of fuel assemblies of nuclear reactors of the same type.

照射燃料から放出される中性子放出率が低い場合には外
部から人為的に中性子源を装着してもよい。また本発明
の方法は、燃料集合体のみならず集合体を構成する1本
1本の核燃料榛の燃焼度測定にも応用できる。
If the neutron emission rate from the irradiated fuel is low, a neutron source may be artificially attached from the outside. Furthermore, the method of the present invention can be applied not only to fuel assemblies but also to measuring the burn-up of each nuclear fuel ray that constitutes the assembly.

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

第1図はBWR原子炉の燃料集合体において熱中性子吸
収断面積と高速中性子減速断面積との比が燃料の燃焼度
によって変化することを示す図、第2図aはBWR原子
炉の燃料集合体の断面図「同図bは直線A−Aにそう高
速中性子と熱中性子の中性子東分布曲線を示す図、第3
図a〜cは燃料集合体の内部または周囲に中性子検出装
置を設置した断面図、第4図は停止中の原子炉炉心内部
に中性子検出装置をそう入した図である。 1・・…・燃焼度曲線、2…・・・曲り〜 3……燃料
集合体、亀……核燃料棒、5・・・・・0チャンネルボ
ックス、6……減速材〜 ?……反射材、8,8a……
中性子検出装置、9……熱中性子誘導体、】0・・・・
・・制御榛。 ゲイ図 才2図 才3図 才千斑
Figure 1 shows how the ratio of the thermal neutron absorption cross section to the fast neutron moderation cross section changes depending on the burnup of the fuel in the fuel assembly of a BWR reactor, and Figure 2 a shows the fuel assembly of a BWR reactor. Cross-sectional view of the body "Figure b is a diagram showing the neutron east distribution curves of fast neutrons and thermal neutrons on the straight line A-A.
Figures a to c are cross-sectional views of a neutron detection device installed inside or around a fuel assembly, and FIG. 4 is a view of the neutron detection device installed inside the reactor core while it is stopped. 1...Burnup curve, 2...Bend~ 3...Fuel assembly, Tortoise...Nuclear fuel rod, 5...0 channel box, 6...Moderator~? ...Reflective material, 8,8a...
Neutron detection device, 9... thermal neutron derivative, ]0...
...control. Gay figure 2 figure figure 3 figure figure Chimura

Claims (1)

【特許請求の範囲】[Claims] 1 多数の核燃料棒からなる燃料集合体と媒質により構
成される体系の、前記燃料集合体の内部または外部の少
なくともいずれか一方において、中性子検出器によりエ
ネルギー的に性質の異なる2種類の中性子束を測定し、
それら中性子束から中性子束比を求め、前記中性子束比
を用いて燃焼度と中性子束比との関係を示す校正曲線か
ら燃料集合体の燃焼度を測定する方法。
1. In a system composed of a fuel assembly consisting of a large number of nuclear fuel rods and a medium, two types of neutron fluxes having different energetic properties are detected by a neutron detector inside or outside of the fuel assembly. measure,
A method of determining the neutron flux ratio from these neutron fluxes, and using the neutron flux ratio to measure the burnup of the fuel assembly from a calibration curve showing the relationship between the burnup and the neutron flux ratio.
JP51127355A 1976-10-25 1976-10-25 Method for measuring burnup of fuel assembly Expired JPS608474B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51127355A JPS608474B2 (en) 1976-10-25 1976-10-25 Method for measuring burnup of fuel assembly

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51127355A JPS608474B2 (en) 1976-10-25 1976-10-25 Method for measuring burnup of fuel assembly

Publications (2)

Publication Number Publication Date
JPS5352894A JPS5352894A (en) 1978-05-13
JPS608474B2 true JPS608474B2 (en) 1985-03-02

Family

ID=14957876

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51127355A Expired JPS608474B2 (en) 1976-10-25 1976-10-25 Method for measuring burnup of fuel assembly

Country Status (1)

Country Link
JP (1) JPS608474B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7336349B2 (en) * 2019-10-11 2023-08-31 三菱重工業株式会社 Subcriticality measuring device and subcriticality measuring method

Also Published As

Publication number Publication date
JPS5352894A (en) 1978-05-13

Similar Documents

Publication Publication Date Title
KR910007146B1 (en) Method and apparatus for determining the nearness to criticality of a nuclear reactor
US8401141B2 (en) Axial void fraction distribution measurement method and neutron multiplication factor evaluating method
JP5752467B2 (en) Reactor fuel non-destructive burnup evaluation method and apparatus
Sasahara et al. Neutron and gamma ray source evaluation of LWR high burn-up UO2and MOX spent fuels
JPS608473B2 (en) Method for measuring burnup of irradiated fuel
JP3103361B2 (en) Measurement method of burnup of nuclear fuel
JP3041101B2 (en) Measurement method of effective multiplication factor of spent fuel assembly loading system
JP2003043183A (en) Heating rate measurement method for irradiated fuel
JPS608474B2 (en) Method for measuring burnup of fuel assembly
JP3026455B2 (en) Burnup measurement method for irradiated fuel assemblies
JPH045356B2 (en)
JP4261011B2 (en) Method and apparatus for measuring change in reactivity and effective resonance integral depending on fuel temperature
JPH04269697A (en) Non-destructive inspection device for reactor fuel rod
JP4664645B2 (en) Method for measuring neutron emission rate of irradiated fuel assemblies
Hachiya et al. Lattice parameter measurements on cluster-type fuel for advanced thermal reactor
JP3115092B2 (en) Effective gain measurement method and neutron detector placement method
Smith et al. Experimental studies of U238 resonance neutron capture in UO2 fuel rods
JPH0426718B2 (en)
JPH0317115B2 (en)
GB917776A (en) Method of measuring the amount of material fissile by thermal neutrons and present in any arbitrary substance, particularly for controlling the state of exhaustion of fuel elements in nuclear reactors
Yokoyama et al. Neutron emission characteristics of spent boiling water reactor fuel
JPS6316298A (en) Nondestructive measuring method of spent nuclear fuel aggregate
JPS6138432B2 (en)
Perret et al. Toward Reanalysis of the Tight-Pitch HCLWR-PROTEUS Phase II Experiments
Spivak et al. Measurements of η for U233, U235 AND Pu239 With epithermal neutrons with epithermal neutrons