JPH0442321B2 - - Google Patents

Info

Publication number
JPH0442321B2
JPH0442321B2 JP61025285A JP2528586A JPH0442321B2 JP H0442321 B2 JPH0442321 B2 JP H0442321B2 JP 61025285 A JP61025285 A JP 61025285A JP 2528586 A JP2528586 A JP 2528586A JP H0442321 B2 JPH0442321 B2 JP H0442321B2
Authority
JP
Japan
Prior art keywords
gas
tritium
zrco
hydrogen
hydride
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
JP61025285A
Other languages
Japanese (ja)
Other versions
JPS62182101A (en
Inventor
Tetsuyuki Konishi
Masatada Nagasaki
Hiroshi Katsuta
Juji Naruse
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.)
Japan Atomic Energy Agency
Original Assignee
Japan Atomic Energy Research Institute
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 Japan Atomic Energy Research Institute filed Critical Japan Atomic Energy Research Institute
Priority to JP61025285A priority Critical patent/JPS62182101A/en
Priority to CA000529235A priority patent/CA1320336C/en
Publication of JPS62182101A publication Critical patent/JPS62182101A/en
Publication of JPH0442321B2 publication Critical patent/JPH0442321B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C16/00Alloys based on zirconium
    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21FPROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F9/00Treating radioactively contaminated material; Decontamination arrangements therefor
    • G21F9/02Treating gases
    • 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
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/32Hydrogen storage

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Hydrogen, Water And Hydrids (AREA)
  • Gas Separation By Absorption (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はトリチウムガスの回収、貯蔵、供給法
に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for collecting, storing and supplying tritium gas.

(従来の技術) 従来、トリチウムを含む水素同位体の混合ガス
(以下単にトリチウムガスと称する)の回収、貯
蔵及び供給には、活性ウラン金属を容器中に封入
した、所謂ウランベツドが広く用いられてきた。
しかしながら、金属ウランは核燃料物質であり、
その入手、加工、及び使用が法的に規制、制限さ
れており、実用上極めて不便である。またウラン
及びその水素化物粉末は化学的に活性であり、空
気中で発火する性質を持つため、この取扱いには
不活性ガス雰囲気を必要とし、事故時の危険性も
大きい。その上、焼結性や他金属と共融する性質
により、水素化による発熱や加熱時の温度制御に
注意する必要があり、取扱いが容易ではない。
(Prior Art) Conventionally, a so-called uranium bed, in which active uranium metal is sealed in a container, has been widely used for the collection, storage, and supply of a mixed gas of hydrogen isotopes containing tritium (hereinafter simply referred to as tritium gas). Ta.
However, uranium metal is a nuclear fuel material;
Its acquisition, processing, and use are legally regulated and restricted, making it extremely inconvenient in practice. Furthermore, since uranium and its hydride powder are chemically active and have the property of igniting in the air, handling them requires an inert gas atmosphere, which poses a high risk in the event of an accident. Furthermore, due to its sinterability and eutectic properties with other metals, it is necessary to pay attention to heat generation due to hydrogenation and temperature control during heating, making it difficult to handle.

以上のウラン金属の欠点を避けるため、Ti、
Zr、Y、ZrAl等の金属や合金が同様の目的で試
みられている。しかしながら、これらの材料はい
ずれも水素化物の平衡分解圧が低く、図1に示す
ように、室温でのトリチウム回収には有用である
が、約1気圧のトリチウムガスを放出させる必要
のある供給時には800℃以上の高温を必要とし、
安定性、特にトリチウム透過の面から500℃以下
が望ましいとされているトリチウム使用機器の材
料としては適さない。最近、金属間化合物の
ZrNiの使用も試みられているが、これは、3水
素化物は平衡分解圧が高く供給の目的に使用でき
るものの、1水素化物は容易に分解しない。この
ため、3水素化物としてはトリチウムを吸収し、
次に、これを放出させる場合、分解により得られ
るトリチウムは吸収された量の2/3であり、残り
1/3は分解しない1水素化物として金属中に残り、
再使用できないため、著しく不経済である。
To avoid the above drawbacks of uranium metal, Ti,
Metals and alloys such as Zr, Y, and ZrAl have been tried for similar purposes. However, all of these materials have low equilibrium decomposition pressures for hydrides, and while they are useful for tritium recovery at room temperature, as shown in Figure 1, they are not suitable for supplying tritium gas that needs to be released at approximately 1 atm. Requires high temperature of 800℃ or more,
It is not suitable as a material for equipment that uses tritium, which is said to be desirably below 500°C in terms of stability, especially tritium permeation. Recently, intermetallic compounds
The use of ZrNi has also been attempted, but the trihydride has a high equilibrium decomposition pressure and can be used for feeding purposes, but the monohydride does not decompose easily. Therefore, as a trihydride, it absorbs tritium,
Next, when releasing tritium, the tritium obtained by decomposition is 2/3 of the absorbed amount, and the remaining 1/3 remains in the metal as a monohydride that does not decompose.
It is extremely uneconomical because it cannot be reused.

(発明が解決しようとする問題点) 本発明の目的は、以下の欠点を除き、核燃料物
質や500℃以上の高温を用いずにトリチウムガス
の回収、貯蔵、供給を一つつの装置で行うことを
可能にするトリチウムガスの回収、貯蔵及び供給
方法を提供することにある。
(Problems to be Solved by the Invention) The purpose of the present invention is to recover, store, and supply tritium gas in one device without using nuclear fuel materials or high temperatures of 500°C or higher, except for the following drawbacks: The purpose of the present invention is to provide a method for recovering, storing, and supplying tritium gas.

(問題点を解決するための手段) 本願発明者は、この目的達成のため鋭意研究の
結果、金属間化合物ZrCoの室温付近における水
素化反応によつて気相中のトリチウムガスを回収
し、水素化物の状態で貯蔵し、これを加熱分解せ
しめて再びトリチウムガスの供給に使用すること
を発想し、本願発明に到達するを得た。
(Means for Solving the Problem) As a result of intensive research to achieve this objective, the inventor of the present application recovered tritium gas in the gas phase through a hydrogenation reaction of the intermetallic compound ZrCo at around room temperature, and hydrogen The present invention was developed based on the idea of storing tritium in the form of tritium, thermally decomposing it, and using it again to supply tritium gas.

即ち、実用上ウランとほぼ同等な水素平衡圧を
持つ物質、金属間化合物ZrCo、又はこれを主成
分とする合金(以下単にZrCoと称する)を用い
て、トリチウムガスを室温付近で10-3Pa程度の
分圧まで回収し、これを水素化物の状態で固定、
貯蔵し、またこれを約400℃まで加熱して回収さ
れたトリチウムを1気圧付近の圧力で供給せんと
するものである。
In other words, tritium gas is heated at 10 -3 Pa at around room temperature using a material that has a hydrogen equilibrium pressure almost equivalent to that of uranium, the intermetallic compound ZrCo, or an alloy mainly composed of ZrCo (hereinafter simply referred to as ZrCo). The partial pressure is recovered to a certain level, and this is fixed in the hydride state.
The plan is to store the tritium, heat it to about 400°C, and then supply the recovered tritium at a pressure of around 1 atmosphere.

本発明で使用するZrCoは粉末、或いは小片と
して密閉容器中に封入する。これにトリチウムガ
スを含む気体を接触、或いは流通させることによ
りZrCoの水素化反応が起りトリチウムガスの回
収が行われる。このとき気相中に残留するトリチ
ウムガスの分圧は室温付近で10-3Pa前後であり、
吸収容量はZrCo1g当たりトリチウムガス約150
c.c.〔NTP〕である。
ZrCo used in the present invention is sealed in a closed container as a powder or small pieces. By contacting or flowing a gas containing tritium gas thereto, a hydrogenation reaction of ZrCo occurs and tritium gas is recovered. At this time, the partial pressure of tritium gas remaining in the gas phase is around 10 -3 Pa near room temperature,
Absorption capacity is approximately 150 tritium gas per gram of ZrCo
cc [NTP].

吸収されたトリチウムガスはZrCo水素化物と
してそのまま貯蔵される。容器内でトリチウムは
ごくわずか気相に残留する他はすべて水素化物と
して固定されるため、漏洩による周囲の汚染や容
器破損時の大量トリチウムガスの放出の危険が少
なく、ガスのままでの貯蔵や、また同じ水素化物
でも自然性、発火性を有するウランの場合に比較
するとより安全である。
The absorbed tritium gas is directly stored as ZrCo hydride. Inside the container, tritium remains in the gas phase, and everything else is fixed as hydride, so there is little risk of contaminating the surrounding area due to leakage or releasing a large amount of tritium gas if the container is broken, and it can be stored as a gas. It is also safer than uranium, which is a natural and flammable hydride.

トリチウムガスの供給は、このZrCo水素化物
を加熱して行われる。この水素化物の平衡分圧は
図1に示すとおりであり、必要なトリチウムガス
の圧力に対応する温度に水素化物を加熱すること
により、純粋なトリチウムガスを得ることができ
る。例えば、1気圧のトリチウムガスを得るには
水素化物を約400℃に加熱すればよく、このとき、
ZrNiの場合のように、1水素化物をつくること
はないので、水素化物中の大部分のトリチウムが
ガスとして放出される。
Tritium gas is supplied by heating this ZrCo hydride. The equilibrium partial pressure of this hydride is as shown in FIG. 1, and pure tritium gas can be obtained by heating the hydride to a temperature corresponding to the required pressure of tritium gas. For example, to obtain tritium gas at 1 atm, hydride can be heated to about 400°C;
Since no monohydride is formed as in the case of ZrNi, most of the tritium in the hydride is released as a gas.

本発明の方法によるトリチウムガスの吸収、放
出を行う装置の例を図2に示す。
An example of an apparatus for absorbing and releasing tritium gas according to the method of the present invention is shown in FIG.

ZrCoは水素化に伴い粉末化する性質があるた
め、飛散を防ぐ図中のように耐熱性のあるフイ
ルター中に保持するのが実用上便利である。
Since ZrCo has the property of turning into powder when hydrogenated, it is practically convenient to hold it in a heat-resistant filter 2 as shown in 1 in the figure to prevent it from scattering.

ほぼ純粋な水素同位体ガスが回収対象の場合
は、ガスは導入口により密封容器中に吸入さ
れ、回収される。水素以外を含む混合ガスが対象
の場合は、ガスを導入口から導入口へZrCo
を通して流通することにより、ガス中の水素同位
体のみが選択的に吸収され、水素をほとんど含ま
ぬガスがより得られる。残留するトリチウム
(水素)の分圧は温度が低いほど低いが作動温度
は室温付近が便利であり、また実際には水素化発
熱により吸収時のZrCoの温度は室温より高いの
が普通である。反応速度が室温で十分大きい。
When substantially pure hydrogen isotope gas is to be recovered, the gas is sucked into the sealed container 6 through the inlet 4 and recovered. If the target is a mixed gas containing other than hydrogen, transfer the gas from inlet 4 to inlet 5 .
By flowing through the gas, only hydrogen isotopes in the gas are selectively absorbed, and a gas containing almost no hydrogen can be obtained from 5 . Although the partial pressure of residual tritium (hydrogen) is lower as the temperature is lower, it is convenient for the operating temperature to be around room temperature, and in reality, the temperature of ZrCo during absorption is usually higher than room temperature due to hydrogenation heat generation. The reaction rate is sufficiently high at room temperature.

回収されたトリチウムの貯蔵は導入口及び導
出口を閉じて行われる。このとき密封容器
中は前述の吸収操作の結果としてほぼ真空または
水素以外のガスのみであり、トリチウム分圧が低
いため万一容器に洩れや破損が生じても大量トリ
チウムの放出は起こらない。
The recovered tritium is stored by closing the inlet 4 and the outlet 5 . At this time, the inside of the sealed container 6 is almost a vacuum or contains only gas other than hydrogen as a result of the above-mentioned absorption operation, and since the partial pressure of tritium is low, even if the container leaks or breaks, a large amount of tritium will not be released. .

トリチウムガスの供給はヒーターに通電して
行われる。温度は前述のように必要なトリチウム
ガスの圧力に応じて設定する。ZrCoが所定温
度に達したときまたはを開放することによつ
て純粋なトリチウムガスが得られる。必要量のト
リチウムガスを取出したのち、又はを閉じヒ
ーターを切れば、容器内のトリチウムガスは
再びZrCoに吸収される。
Tritium gas is supplied by energizing the heater 3 . The temperature is set according to the required pressure of tritium gas as described above. Pure tritium gas is obtained by opening 4 or 5 when ZrCo 1 reaches a predetermined temperature. After taking out the required amount of tritium gas, if 4 or 5 is closed and the heater 3 is turned off, the tritium gas in the container 6 will be absorbed into ZrCo again.

以上のようにトリチウムガスの回収、貯蔵、供
給は、本発明の方法により一つの装置で高温を用
いずに行なうことができる。材料であるZrCoは
ウランと異なり、核燃料物質でも放射性物質でも
なく、しかも空気中での発火性を有しないので容
易に取扱うことができ、安全性も高く、また安価
である。なお、上述の一連の操作はまた、低分圧
の、或いは希薄なトリチウムガスを分離、回収
し、また精製、昇圧する方法としても利用可能で
ある。
As described above, tritium gas can be recovered, stored, and supplied by the method of the present invention in one device without using high temperatures. Unlike uranium, the material ZrCo is neither a nuclear fuel material nor a radioactive material, and it is not flammable in the air, so it is easy to handle, highly safe, and inexpensive. Note that the above series of operations can also be used as a method for separating and recovering low partial pressure or dilute tritium gas, as well as for purifying and pressurizing it.

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

第1図は、本発明と同種目的への使用が考えら
れる各種物質の平衡水素圧、つまり物質と水素が
接して吸収または放出が起こり平衡に達している
ときの気相での水素分圧の温度変化を表わす。例
えば、ZrCoは50℃のときは気相の水素分圧が
10-3tarrになるまで水素を吸収または放出する。
ZrNi、Ti、Zrは600℃以下では1気圧以上の圧力
の水素を放出することはできない。第2図は、本
発明の実施例を図示したものである。 図において、1…ZrCo、2…フイルター、3
…ヒーター線、4…ガス導入口、5…ガス導出
口、6…密封容器。
Figure 1 shows the equilibrium hydrogen pressure of various substances considered to be used for the same purpose as the present invention, that is, the hydrogen partial pressure in the gas phase when the substance and hydrogen come into contact and absorption or release occurs and equilibrium is reached. Represents temperature change. For example, for ZrCo, when the temperature is 50℃, the hydrogen partial pressure in the gas phase is
It absorbs or releases hydrogen up to 10 -3 tarr.
ZrNi, Ti, and Zr cannot release hydrogen at a pressure of 1 atmosphere or more at temperatures below 600°C. FIG. 2 illustrates an embodiment of the invention. In the figure, 1...ZrCo, 2...filter, 3
... Heater wire, 4... Gas inlet, 5... Gas outlet, 6... Sealed container.

Claims (1)

【特許請求の範囲】[Claims] 1 金属間化合物ZrCo、又はこれを主成分とす
る合金との水素化反応により気相中のトリチウム
を含む水素同位体ガスを回収し、これを水素化物
として貯蔵し、またこれを加熱、分解せしめるこ
とによつて再びトリチウムガスの供給を行うこと
を特徴とするトリチウムガスの回収、貯蔵及び供
給法。
1. Collect tritium-containing hydrogen isotope gas in the gas phase through a hydrogenation reaction with the intermetallic compound ZrCo or an alloy containing ZrCo as a main component, store this as a hydride, and heat and decompose it. A method for recovering, storing and supplying tritium gas, characterized by supplying tritium gas again.
JP61025285A 1986-02-07 1986-02-07 Method for recovery, storage and supply of tritium gas Granted JPS62182101A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP61025285A JPS62182101A (en) 1986-02-07 1986-02-07 Method for recovery, storage and supply of tritium gas
CA000529235A CA1320336C (en) 1986-02-07 1987-02-06 Method of recovery, storage and supply of gaseous tritium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61025285A JPS62182101A (en) 1986-02-07 1986-02-07 Method for recovery, storage and supply of tritium gas

Publications (2)

Publication Number Publication Date
JPS62182101A JPS62182101A (en) 1987-08-10
JPH0442321B2 true JPH0442321B2 (en) 1992-07-13

Family

ID=12161748

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61025285A Granted JPS62182101A (en) 1986-02-07 1986-02-07 Method for recovery, storage and supply of tritium gas

Country Status (2)

Country Link
JP (1) JPS62182101A (en)
CA (1) CA1320336C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03134131A (en) * 1989-10-18 1991-06-07 Japan Metals & Chem Co Ltd Alloy for handling isotope of hydrogen
WO2016034745A2 (en) * 2015-09-22 2016-03-10 Cylenchar Limited A method for concentrating and/or entrapping radioisotopes from an aqueous solution
CN112226663B (en) * 2020-10-20 2021-10-29 浙江大学 ZrCo-based hydrogen isotope storage alloy with high cycle capacity and its preparation and application

Also Published As

Publication number Publication date
JPS62182101A (en) 1987-08-10
CA1320336C (en) 1993-07-20

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