JPH0222356B2 - - Google Patents
Info
- Publication number
- JPH0222356B2 JPH0222356B2 JP14398281A JP14398281A JPH0222356B2 JP H0222356 B2 JPH0222356 B2 JP H0222356B2 JP 14398281 A JP14398281 A JP 14398281A JP 14398281 A JP14398281 A JP 14398281A JP H0222356 B2 JPH0222356 B2 JP H0222356B2
- Authority
- JP
- Japan
- Prior art keywords
- neutron
- piping
- multiplication
- shield
- nuclear fuel
- 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
Links
- 238000012545 processing Methods 0.000 claims description 16
- 238000012958 reprocessing Methods 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 11
- 230000002269 spontaneous effect Effects 0.000 claims description 8
- 239000003758 nuclear fuel Substances 0.000 claims description 7
- 230000005251 gamma ray Effects 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 3
- 238000012544 monitoring process Methods 0.000 claims description 3
- 239000006096 absorbing agent Substances 0.000 claims description 2
- 230000004907 flux Effects 0.000 claims 4
- 238000012806 monitoring device Methods 0.000 claims 2
- 230000000694 effects Effects 0.000 description 5
- 230000004992 fission Effects 0.000 description 3
- 239000002915 spent fuel radioactive waste Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
Classifications
-
- 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
-
- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
Landscapes
- Monitoring And Testing Of Nuclear Reactors (AREA)
Description
【発明の詳細な説明】
本発明は核燃料再処理系(以下再処理系)の未
臨界性監視法および装置に係る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a subcriticality monitoring method and apparatus for a nuclear fuel reprocessing system (hereinafter referred to as a reprocessing system).
使用済燃料中には、核分裂性核種であるU−
235,Pu−239等や自発中性子を放出する核種で
あるCm−242,Cm−244,Pu−238、Pu−240が
混在し、さらに強いガンマ線を放出する核分裂生
成核種が混在する。再処理系で使用済燃料は、硝
酸に溶解され液化され処理液とされるが、この液
中には前記各核種と共に減速材となる水素が含ま
れている。自発中性子はU−235,Pu−239等に
吸収された核分裂を誘発する。すなわち、処理液
は中性子増倍体系となつている。したがつて、
Pu−239やU−235の濃度が高い場合とか、配管
や処理槽が大きい場合には、それらの内部の処理
液を未臨界に保持することが安全上きわめて重要
である。 Spent fuel contains U-, a fissile nuclide.
235, Pu-239, etc., nuclides that emit spontaneous neutrons, such as Cm-242, Cm-244, Pu-238, and Pu-240, are mixed, as well as fission-produced nuclides that emit even stronger gamma rays. In the reprocessing system, spent fuel is dissolved in nitric acid and liquefied to form a treatment liquid, which contains hydrogen, which serves as a moderator, along with the above-mentioned nuclides. Spontaneous neutrons induce nuclear fission absorbed by U-235, Pu-239, etc. In other words, the processing liquid has a neutron multiplication system. Therefore,
When the concentration of Pu-239 or U-235 is high, or when the piping or processing tank is large, it is extremely important for safety to maintain the processing liquid inside the subcritical state.
ところで、使用済燃料再処理溶液の中には核分
裂生成物(FP)の他に、核分裂性核種U−235,
Pu−239,Pu−241および核分裂を殆ど起こさな
いPu−238,Pu−240等が含まれている。また、
極く微量ながらCm−242やCm−244等が含まれ
ている。これらはkeff値に顕著に影響を与えるも
の(U−235,Pu−239,Pu−241)と、keff値に
は殆ど影響がなく、自発中性子放出率の高いもの
(Cm−242,Cm−244,Pu−240,Pu−238)に
分類できる。 By the way, in addition to fission products (FP), the spent fuel reprocessing solution contains fissile nuclides U-235,
It contains Pu-239, Pu-241, and Pu-238, Pu-240, which hardly cause nuclear fission. Also,
It contains elements such as Cm-242 and Cm-244, although in extremely small amounts. These include those that significantly affect the k eff value (U-235, Pu-239, Pu-241) and those that have a high spontaneous neutron emission rate (Cm-242, Cm −244, Pu−240, Pu−238).
再処理溶液系から放出される中性子を測定する
と、keffに依存する因子と自発中性子放出率の大
きさに比例する因子との積に比例した値が得られ
る。ところが、後者はkeffには事実上殆ど影響が
ないので、後者の効果を相殺しないと未臨界度を
正しく監視することはできない。例えば、keff値
が大きくてもCm−242,Cm−244,Pu−240,
Pu−238等の濃度が低いと、中性子計数率は比較
的小さくなり、一見安全のように見えても臨界に
近付いているおそれもあり得る。 When measuring the neutrons emitted from the reprocessing solution system, a value proportional to the product of a factor dependent on k eff and a factor proportional to the magnitude of the spontaneous neutron emission rate is obtained. However, since the latter has virtually no effect on k eff , the degree of subcriticality cannot be correctly monitored unless the latter effect is canceled out. For example, even if the k eff value is large, Cm−242, Cm−244, Pu−240,
When the concentration of Pu-238 etc. is low, the neutron count rate becomes relatively low, and even if it appears safe at first glance, there is a possibility that it may approach criticality.
本発明は上記の事情に基きなされたもので、自
発中性子放出核種の濃度如何に拘らず、高精度で
未臨界性を監視し得る再処理系の未臨界性監視法
および装置を得ることを目的としている。 The present invention was made based on the above circumstances, and an object thereof is to provide a subcriticality monitoring method and device for a reprocessing system that can monitor subcriticality with high accuracy regardless of the concentration of spontaneous neutron-emitting nuclides. It is said that
本発明においては、再処理系に必要な配管に対
し、中性子増倍率が特に小さくなるようにした流
路を並列または直列に設け、前記流路における中
性子計数率を用いて、前記配管の中性子計数率か
ら配管内を流れる処理中の自発中性子放出核種濃
度変化の効果を除去する如くして前記目的を達成
している。 In the present invention, a flow path whose neutron multiplication factor is particularly small is provided in parallel or in series with the piping necessary for the reprocessing system, and the neutron counting rate of the piping is performed using the neutron count rate in the flow path. The above objective is achieved by removing from the rate the effect of changes in the concentration of spontaneous neutron-emitting nuclides flowing through the pipe during processing.
以下、本発明の詳細を説明する。いま、同一組
成の処理液が中性子増倍効果がほぼ無視できる流
路(以下A流路)と、無視できない流路(以下B
流路)とをそれぞれ流れているものとする。 The details of the present invention will be explained below. Now, when processing liquids with the same composition are used, there is a channel in which the neutron multiplication effect can be almost ignored (hereinafter referred to as channel A), and a channel in which the neutron multiplication effect cannot be ignored (hereinafter referred to as channel B).
It is assumed that the flow path) and the flow path are respectively flowing.
A流路、B流路で測定した中性子計数率をそれ
ぞれφ0,φとし、実効増倍率をそれぞれk0,k
比例定数をそれぞれα0,αとすると、
φ0=α0S0/1−k0 …(1)
φ0=αS/1−k …(2)
となる。なお、式(1),(2)中S0,Sは単位体積当り
の中性子放出率である。而して、前記したように
同一組成の処理液が両流路を流れるのであるか
ら、S=S0であり、
式(1),(2)の比から
k=1−(α/α0)(φ0/φ)(1−k0) …(3)
が得られる。 Let the neutron count rates measured in the A channel and the B channel be φ 0 and φ, respectively, and the effective multiplication factors are k 0 and k, respectively.
When the proportionality constants are α 0 and α, respectively, φ 0 =α 0 S 0 /1−k 0 (1) φ 0 =αS/1−k (2). Note that S 0 and S in equations (1) and (2) are neutron emission rates per unit volume. As mentioned above, since the processing liquid with the same composition flows through both flow paths, S=S 0 , and from the ratio of equations (1) and (2), k=1−(α/α 0 )(φ 0 /φ) (1−k 0 ) …(3) is obtained.
式(3)中のφ0,φは測定により求める。また、
A流路の流路断面積を小さくしたり、流路中に中
性子吸収体を配置したりしてk0<<1となるよう
にし、種々の組成の処理液を用いて実験と解析を
行なうことによりα/α0を求める。前記の如くk0
<<1を実現すれば、式(3)は
k≒1−(α/α0)(φ/φ0) …(4)
となり、上記の如くして求めたφ0,φ,α/α0
を式(4)に代入してkを得ることができる。 φ 0 and φ in equation (3) are determined by measurement. Also,
Experiments and analyzes will be conducted using treatment liquids of various compositions by reducing the cross-sectional area of channel A and placing a neutron absorber in the channel so that k 0 <<1. Find α/α 0 by As mentioned above, k 0
If <<1 is realized, equation (3) becomes k≒1−(α/α 0 )(φ/φ 0 ) …(4), and φ 0 , φ, α/α obtained as above 0
k can be obtained by substituting into equation (4).
次に、処理槽の増倍率kxも、
kx=1−(αx/α)(φ/φx)(1−k) …(5)
で与えられる式(5)中kは式(4)により与えられる。
また、φ,φxは測定により求め、αx/αは計算
により求められる。 Next, the multiplication factor k x of the treatment tank is also given by k x = 1 - (αx / α) (φ / φx) (1 - k) ... (5) In equation (5), k is given by equation (4) is given by
Further, φ and φx are determined by measurement, and αx/α is determined by calculation.
本発明においては上記の如くして配管または処
理槽の未臨界度を監視する。 In the present invention, the subcriticality of the piping or treatment tank is monitored as described above.
以下、図面につき本発明の実施例を説明する。 Embodiments of the present invention will be described below with reference to the drawings.
第1図において、再処理系の配管1に並列に分
岐管2が設けてあり、この分岐管2にはU字状の
屈曲部2aが設けてある。なお、U字状の屈曲部
2aに両脚片は配管1とU字状の底部に相当する
分岐管の直状部との間に配置した中性子遮蔽体3
を貫通している。なお、配管1および前記直状部
には、それぞれガンマ線遮蔽体4,5で包囲した
中性子検出器6,7が対向されている。 In FIG. 1, a branch pipe 2 is provided in parallel with a pipe 1 of a reprocessing system, and this branch pipe 2 is provided with a U-shaped bent portion 2a. In addition, both leg pieces of the U-shaped bent part 2a are neutron shielding bodies 3 arranged between the pipe 1 and the straight part of the branch pipe corresponding to the bottom of the U-shape.
penetrates through. Note that neutron detectors 6 and 7 surrounded by gamma ray shields 4 and 5 are opposed to the pipe 1 and the straight portion.
上記の構成において、分岐管2の流路断面積を
小とし配管1内を流れる処理液が分流した時の増
倍率が特に小さくなるようにしておけば、検出器
6,7の出力を用い、前記式(3)〜(4)につき説明し
たのと同様にして、配管1の増倍率kを求めるこ
とができ、処理液中の自発中性子放出核種の濃度
如何に拘らず、配管1の未臨界度を正確に監視、
評価することができる。 In the above configuration, if the cross-sectional area of the branch pipe 2 is made small so that the multiplication factor when the processing liquid flowing in the pipe 1 is divided is particularly small, the outputs of the detectors 6 and 7 can be used to The multiplication factor k of the pipe 1 can be determined in the same manner as explained for the above equations (3) to (4), and regardless of the concentration of spontaneous neutron-emitting nuclides in the processing liquid, the subcriticality of the pipe 1 can be determined. Accurately monitor the degree of
can be evaluated.
第2図は本発明の他の実施例を示す。この実施
例では分岐管2に代え、配管1内にB4Cなどの中
性子吸収材から成る中空円筒状の増倍抑制体8が
設置してある。また、検出器6は増倍抑制体8が
ない位置において、検出器7は増倍抑制体8があ
る位置においてそれぞれ配管1に対向されてい
る。なお、配管1には、増倍抑制体8の両端に対
向する位置にフランジ状の中性子遮蔽体9,10
が取り付けられている。 FIG. 2 shows another embodiment of the invention. In this embodiment, instead of the branch pipe 2, a hollow cylindrical multiplication suppressor 8 made of a neutron absorbing material such as B 4 C is installed inside the pipe 1. Further, the detector 6 is opposed to the pipe 1 at a position where the multiplication suppressor 8 is not present, and the detector 7 is opposed to the pipe 1 at a position where the multiplication suppressor 8 is present. The piping 1 is provided with flange-shaped neutron shields 9 and 10 at positions facing both ends of the multiplication suppressor 8.
is installed.
この実施例にあつては、配管1の一部に増倍抑
制体8が設けてあるので、その部分の増倍率k0は
他の部分のそれより小となる。増倍抑制体8の大
きさ、肉厚、その組成等を適宜選定し、k<<1
とすれば増倍抑制体8を配置した部分は、第1図
の実施例の分岐管2と同様に取扱うことができ、
前記実施例と同様にして配管1の未臨界性を監視
することができる。 In this embodiment, since the multiplication suppressor 8 is provided in a part of the pipe 1, the multiplication factor k 0 in that part is smaller than that in other parts. The size, thickness, composition, etc. of the multiplication suppressor 8 are appropriately selected, and k<<1.
If so, the part where the multiplication suppressor 8 is arranged can be handled in the same way as the branch pipe 2 of the embodiment shown in FIG.
The subcriticality of the pipe 1 can be monitored in the same manner as in the previous embodiment.
第3図は本発明の第3の実施例を示す。この図
において、第1図の実施例における配管1は、そ
の一端において処理槽11に開口しており、処理
槽11にはガンマ線遮蔽体12に包囲された中性
子検出器13が対向されている。 FIG. 3 shows a third embodiment of the invention. In this figure, the piping 1 in the embodiment of FIG. 1 opens into a processing tank 11 at one end, and a neutron detector 13 surrounded by a gamma ray shield 12 is opposed to the processing tank 11.
この実施例では、第1図に示した実施例により
求めた配管の増倍率kおよび検出器13の出力を
用いて、前記の式(5)によつて、処理槽11の増倍
率kxを求めることができ、処理槽11の未臨界度
を正確に監視、評価することができる。 In this embodiment, the multiplication factor k x of the processing tank 11 is calculated by the above equation (5) using the multiplication factor k of the piping obtained in the embodiment shown in FIG. 1 and the output of the detector 13. The degree of subcriticality of the processing tank 11 can be accurately monitored and evaluated.
第1図、第2図、第3図はそれぞれ本発明の第
1、第2、第3の実施例の模式図である。
1……配管、2……分岐管、3,9,10……
中性子遮蔽体、4,6,12……ガンマ線遮蔽
体、6,7,13……中性子検出器、8……増倍
抑制体、11……処理槽。
FIG. 1, FIG. 2, and FIG. 3 are schematic diagrams of the first, second, and third embodiments of the present invention, respectively. 1... Piping, 2... Branch pipe, 3, 9, 10...
Neutron shield, 4, 6, 12... Gamma ray shield, 6, 7, 13... Neutron detector, 8... Multiplication suppressor, 11... Processing tank.
Claims (1)
される中性子束と、上記処理液と同じ組成の処理
液が流れ、中性子増倍率を特に小さくした流路か
ら放出される中性子束とを測定し、それらの中性
子束の比を求め、中性子計数率の自発中性子放出
核種の濃度依存性を除去したことを特徴とする核
燃料再処理系の未臨界性監視法。 2 核燃料再処理系配管に中性子増倍率が特に小
さくなるよう小径とした分岐管を設け、この分岐
管と上記配管との間には中性子遮蔽体を設け、上
記分岐管の側面で上記中性子遮蔽体の反対側およ
び上記配管の側面で上記中性子遮蔽体の反対側
に、ガンマ線遮蔽体で包囲した中性子検出器をそ
れぞれ配置したことを特徴とする核燃料再処理系
の未臨界性監視装置。 3 核燃料再処理系配管内の一部に中性子吸収体
から成る増倍抑制体を配置し、配管の増倍抑制体
のない位置およびある位置に、ガンマ線遮蔽体で
包囲された中性子検出器をそれぞれ対向させ、各
中性子検出器間には中性子遮蔽体を配置したこと
を特徴とする核燃料再処理系の未臨界性監視装
置。[Claims] 1. Neutron flux emitted from nuclear fuel reprocessing system piping through which a processing liquid flows, and neutron flux emitted from a flow path in which a processing liquid having the same composition as the processing liquid flows and has a particularly low neutron multiplication factor. A subcriticality monitoring method for a nuclear fuel reprocessing system, characterized in that the dependence of the neutron count rate on the concentration of spontaneous neutron emitting nuclides is removed by measuring the neutron fluxes and the neutron fluxes. 2 A branch pipe with a small diameter is provided in the nuclear fuel reprocessing system piping so that the neutron multiplication factor is particularly small, a neutron shield is provided between this branch pipe and the above piping, and the neutron shield is installed on the side of the branch pipe. A subcriticality monitoring device for a nuclear fuel reprocessing system, characterized in that a neutron detector surrounded by a gamma ray shield is disposed on the opposite side of the neutron shield and on the side of the piping opposite to the neutron shield. 3 A multiplication suppressor made of a neutron absorber is placed in a part of the nuclear fuel reprocessing system piping, and a neutron detector surrounded by a gamma ray shield is placed in the piping at a position without the multiplication suppressor and at a position where the multiplication suppressor is located. 1. A subcriticality monitoring device for a nuclear fuel reprocessing system, characterized in that neutron detectors are faced to each other and a neutron shield is placed between each neutron detector.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56143982A JPS5845599A (en) | 1981-09-14 | 1981-09-14 | Method and device for monitoring sub-criticality of nuclear fuel reprocessing system |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56143982A JPS5845599A (en) | 1981-09-14 | 1981-09-14 | Method and device for monitoring sub-criticality of nuclear fuel reprocessing system |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5845599A JPS5845599A (en) | 1983-03-16 |
| JPH0222356B2 true JPH0222356B2 (en) | 1990-05-18 |
Family
ID=15351558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56143982A Granted JPS5845599A (en) | 1981-09-14 | 1981-09-14 | Method and device for monitoring sub-criticality of nuclear fuel reprocessing system |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5845599A (en) |
-
1981
- 1981-09-14 JP JP56143982A patent/JPS5845599A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5845599A (en) | 1983-03-16 |
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