JPH1085582A - Reaction vessel for solid-gas reaction powder - Google Patents

Reaction vessel for solid-gas reaction powder

Info

Publication number
JPH1085582A
JPH1085582A JP8262502A JP26250296A JPH1085582A JP H1085582 A JPH1085582 A JP H1085582A JP 8262502 A JP8262502 A JP 8262502A JP 26250296 A JP26250296 A JP 26250296A JP H1085582 A JPH1085582 A JP H1085582A
Authority
JP
Japan
Prior art keywords
gas
reaction
solid
hydrogen
storage alloy
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.)
Granted
Application number
JP8262502A
Other languages
Japanese (ja)
Other versions
JP3640476B2 (en
Inventor
Hiroyuki Mitsui
宏之 三井
Hiroshi Aoki
博史 青木
Hideto Kubo
秀人 久保
Takashi Fuji
敬司 藤
Nobuo Fujita
信雄 藤田
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.)
Toyota Industries Corp
Toyota Motor Corp
Toyota Central R&D Labs Inc
Original Assignee
Toyota Motor Corp
Toyota Central R&D Labs Inc
Toyoda Automatic Loom Works 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 Toyota Motor Corp, Toyota Central R&D Labs Inc, Toyoda Automatic Loom Works Ltd filed Critical Toyota Motor Corp
Priority to JP26250296A priority Critical patent/JP3640476B2/en
Publication of JPH1085582A publication Critical patent/JPH1085582A/en
Application granted granted Critical
Publication of JP3640476B2 publication Critical patent/JP3640476B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/32Hydrogen storage

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  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
  • Hydrogen, Water And Hydrids (AREA)

Abstract

(57)【要約】 【課題】 固気反応粉末の膨張に伴う応力の集中を抑制
し,反応ガスの流通と熱交換を効率的に行うことの出来
る小形で高性能の反応容器の提供。 【解決手段】 反応容器1は,固気反応粉末(水素吸蔵
合金81)を収容する容器11と,容器を上下方向に複
数の区画に区分し固気反応粉末を載置し且つ反応ガスを
透過することのできる仕切り棚15と,熱媒を流通させ
固気反応粉末と熱交換を行う伝熱管21と,伝熱管21
に装着され固気反応粉末と熱媒との間の伝熱を促進する
伝熱フィン25と,反応ガスを導入又は排出させるガス
管と,容器内の反応ガスを透過させ上記ガス管と連結さ
れているガス透過管35とを有する。伝熱管21は,各
区画内の固気反応粉末に接するよう配置されている。
PROBLEM TO BE SOLVED: To provide a small, high-performance reaction vessel capable of suppressing the concentration of stress accompanying expansion of a gas-solid reaction powder and efficiently carrying out reaction gas flow and heat exchange. SOLUTION: A reaction vessel 1 has a vessel 11 for accommodating a solid-gas reaction powder (hydrogen storage alloy 81), and the vessel is vertically divided into a plurality of sections, on which the solid-gas reaction powder is placed and a reaction gas is permeated. A heat transfer tube 21 through which a heat medium flows and exchanges heat with the solid-gas reaction powder;
A heat transfer fin 25 mounted on the tub for promoting heat transfer between the solid-gas reaction powder and the heat medium, a gas pipe for introducing or discharging the reaction gas, and a gas pipe for allowing the reaction gas in the vessel to permeate and being connected to the gas pipe. And a gas permeable tube 35. The heat transfer tubes 21 are arranged so as to be in contact with the solid-gas reaction powder in each section.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【技術分野】本発明は,水素吸蔵合金等の固気反応粉末
の反応容器に関する。
TECHNICAL FIELD The present invention relates to a reaction vessel for a solid-gas reaction powder such as a hydrogen storage alloy.

【0002】[0002]

【従来技術】水素吸蔵合金の反応容器を小形化し,水素
の吸蔵と放出を効率的に行うには,水素吸蔵時の発熱を
効率良く外部に取り除き,水素放出時の反応熱を外部か
ら効率良く供給してやらなければならない。それに加え
て,水素吸蔵合金は,水素の吸蔵時に膨張し,水素放出
時に収縮するから,容器は水素吸蔵合金の膨張収縮によ
る応力に耐えなければならない。
2. Description of the Related Art In order to reduce the size of a hydrogen storage alloy reaction vessel and efficiently store and release hydrogen, heat generated during hydrogen storage is efficiently removed to the outside, and the reaction heat during hydrogen release is efficiently reduced from the outside. I have to supply it. In addition, since the hydrogen storage alloy expands when storing hydrogen and contracts when releasing hydrogen, the container must withstand the stress caused by the expansion and contraction of the hydrogen storage alloy.

【0003】そのため,例えば図11に示すように,水
素吸蔵合金の反応容器9は,円筒形の容器90とし,内
部に可撓性の熱媒細管91を多数配置して熱交換を促進
すると共に,水素透過性のフィルターからなるガス透過
管92を配置し,水素ガスを導入又は導出する。同図に
おいて,符号911は伝熱フィンである。
For this reason, as shown in FIG. 11, for example, a hydrogen-absorbing alloy reaction vessel 9 is a cylindrical vessel 90 in which a large number of flexible heating medium thin tubes 91 are disposed to promote heat exchange. A gas permeable tube 92 composed of a hydrogen permeable filter is arranged to introduce or discharge hydrogen gas. In the figure, reference numeral 911 denotes a heat transfer fin.

【0004】また,水素吸蔵合金の初期活性化,即ち水
素吸蔵合金を加熱脱気と加圧吸蔵の繰り返しにより水素
吸蔵可能にする過程において,一般的に水素吸蔵合金が
微粉化するため,特に容器底部において発生する水素吸
蔵合金の圧密化の不具合にも対応するものでなければな
らない。即ち,水素吸蔵合金が部分的に圧密化すると応
力が一部に集中したり,水素ガスの流れを閉塞化する等
の不具合を生ずるから,これを防止またはこれに対処で
きるようにしなければならない。
[0004] In addition, during the initial activation of the hydrogen storage alloy, that is, in the process of enabling the hydrogen storage alloy to store hydrogen by repeating heating and deaeration and pressurization storage, the hydrogen storage alloy is generally pulverized. It must also cope with the problem of consolidation of the hydrogen storage alloy occurring at the bottom. In other words, if the hydrogen storage alloy is partially consolidated, problems such as concentration of stress locally or blockage of the flow of hydrogen gas occur. Therefore, it is necessary to prevent or cope with such problems.

【0005】そして,特開平7−286794号公報で
は,容器の下部に断熱性の緩衝部を設ける方法が提案さ
れている。また,特開平7−269795号公報には,
水素吸蔵合金を充填し水素吸蔵合金の膨張力を受ける内
部分割容器を容器内に複数設け,この内部分割容器と外
殻を構成する容器とにより反応容器を構成する方法が提
案されている。そして,水素吸蔵合金の膨張力は,複数
の内部分割容器が負担し,反応ガスの圧力は外殻の容器
が受容する。
[0005] Japanese Patent Application Laid-Open No. 7-286794 proposes a method in which a heat insulating buffer is provided at a lower portion of a container. Also, Japanese Patent Application Laid-Open No. Hei 7-269975 discloses that
A method has been proposed in which a plurality of internal divided containers are provided in a container filled with a hydrogen storage alloy and receive the expansion force of the hydrogen storage alloy, and a reaction container is constituted by the internal divided containers and a container constituting an outer shell. Then, the expansion force of the hydrogen storage alloy is borne by the plurality of inner divided containers, and the pressure of the reaction gas is received by the outer shell container.

【0006】[0006]

【解決しようとする課題】しかしながら,従来の水素吸
蔵合金の反応容器には,次のような問題がある。図11
に示す反応容器9は,水素吸蔵合金の活性化時に容器9
0の下方に水素吸蔵合金の部分的な圧密化が生じ,水素
の流れを阻害する閉塞領域等が生じやすいという問題が
ある。そのため,水素ガスの拡散が妨げられると共に水
素吸蔵合金の体積膨張による応力がそこに集中し,また
反応熱の熱交換能力も低下する。
However, the conventional hydrogen storage alloy reaction vessel has the following problems. FIG.
The reaction vessel 9 shown in FIG.
There is a problem that the hydrogen storage alloy is partially densified below 0, and a closed region or the like that obstructs the flow of hydrogen is easily generated. Therefore, the diffusion of hydrogen gas is hindered, and the stress due to the volume expansion of the hydrogen storage alloy is concentrated thereon, and the heat exchange capacity of the reaction heat is also reduced.

【0007】また,断熱性の緩衝材を設ける方法(特開
平7−286794号公報)や,複数の内部分割容器を
容器の内部に設ける方法(特開平7−269795号公
報)は,反応に関与しない無駄な空間が増大し,容器が
大形化するという問題がある。本発明は,かかる従来の
問題点に鑑みてなされたものであり,固気反応粉末の膨
張に伴う応力の集中を抑制し,反応の進行と熱交換を効
率的に行うことの出来る小形で高性能の反応容器を提供
しようとするものである。
Further, a method of providing a heat insulating cushioning material (Japanese Patent Application Laid-Open No. 7-286794) and a method of providing a plurality of internal divided containers inside the container (Japanese Patent Application Laid-Open No. 7-269797) are involved in the reaction. There is a problem that the useless space increases and the container becomes large. SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned conventional problems, and it is a small and highly efficient device capable of suppressing the concentration of stress due to the expansion of the solid-gas reaction powder and efficiently conducting the reaction and heat exchange. It is intended to provide a reaction vessel of high performance.

【0008】[0008]

【課題の解決手段】本発明は,固気反応粉末に反応ガス
を吸脱させる反応容器であって,固気反応粉末を収容し
外殻を形成する容器と,容器を上下方向に複数の区画に
区分すると共に上記固気反応粉末を載置し反応ガスを透
過することのできる仕切り棚と,熱媒を流通させ上記固
気反応粉末と熱交換を行う伝熱管と,この伝熱管に装着
され固気反応粉末と熱媒との間の伝熱を促進する伝熱フ
ィンと,上記容器の内と外との間に反応ガスを導入又は
排出させるガス管と,容器内の反応ガスを透過させ上記
ガス管と連結されているガス透過管とを有しており,上
記伝熱管は,上記仕切り棚によって分けられた各区画内
の固気反応粉末に接するよう配置されていることを特徴
とする固気反応粉末の反応容器にある。
The present invention relates to a reaction vessel for absorbing and desorbing a reaction gas into a gas-solid reaction powder, comprising a container for containing the gas-solid reaction powder to form an outer shell, and a plurality of compartments arranged vertically. A partition shelf on which the solid-gas reaction powder is placed and through which the reaction gas can pass, a heat transfer tube which circulates a heat medium and exchanges heat with the solid-gas reaction powder, and is mounted on the heat transfer tube. A heat transfer fin for promoting heat transfer between the solid-gas reaction powder and the heating medium, a gas pipe for introducing or discharging a reaction gas between the inside and the outside of the container, and a passage for allowing the reaction gas in the container to pass therethrough. A gas permeable tube connected to the gas tube, wherein the heat transfer tube is arranged so as to be in contact with the solid-gas reaction powder in each section divided by the partition shelf. It is in the reaction vessel for the solid-gas reaction powder.

【0009】本発明にかかる反応容器は,仕切り棚によ
って容器内が上下方向に配置された複数の区画によって
区分されている。容器内を上下方向に区分けすることに
より,水素吸蔵合金等の固気反応粉末が一部に偏在せず
均一に分散する。そのため,例えば水素吸蔵合金の初期
活性化により微粉化した場合に,粉末が一部で圧密化す
るような不具合が生じにくくなる。そのため,固気反応
粉末の応力が一部に集中することがなく,固気反応粉末
から放出または吸蔵される反応ガスはスムースに拡散す
る。
The reaction vessel according to the present invention is divided into a plurality of compartments vertically arranged in the vessel by a partition shelf. By dividing the inside of the container in the vertical direction, the solid-gas reaction powder such as a hydrogen storage alloy is uniformly dispersed without being partially distributed. Therefore, for example, when the hydrogen storage alloy is pulverized by the initial activation, a problem that the powder partially consolidates hardly occurs. Therefore, the stress of the gas-solid reaction powder does not concentrate on a part, and the reaction gas released or occluded from the gas-solid reaction powder diffuses smoothly.

【0010】また,仕切り棚は反応ガスを透過させるか
ら,容器内に反応ガスがムラなく満たされることにな
る。そして,各区画内における固気反応粉末の膨張力
は,各区画毎に吸収することになり,応力は全体に分散
される。そして,各区画は,閉じた入れ物等ではなく仕
切り棚によって区分けされるだけであるから,各区画の
間に無駄なスペースが生ぜず,固気反応粉末を容器内に
無駄なく収容することが出来るから,容器を小形化する
ことができる。
[0010] Further, since the reaction gas permeates the partition shelf, the reaction gas is uniformly filled in the container. Then, the expansion force of the solid-gas reaction powder in each section is absorbed in each section, and the stress is dispersed throughout. Since each section is separated by a partition shelf instead of a closed container, no wasteful space is created between the sections and the solid-gas reaction powder can be stored in the container without waste. Therefore, the size of the container can be reduced.

【0011】また,容器に注入または抽出される反応ガ
スは,ガス透過性フィルターのガス透過管とガス管とを
介して行われる。一方,伝熱管は,上記仕切り棚によっ
て分けられた各区画毎にそれぞれの固気反応粉末に接す
るよう配置されているから,反応促進に必要な熱交換を
効率的に行うことができ,固気反応粉末の反応を促進す
る。
Further, the reaction gas injected or extracted into the container is supplied through a gas permeable pipe and a gas pipe of a gas permeable filter. On the other hand, since the heat transfer tubes are arranged so as to be in contact with the solid-gas reaction powder in each section divided by the partition shelf, the heat exchange required for promoting the reaction can be performed efficiently, and the solid-gas Promotes the reaction of the reaction powder.

【0012】上記の結果,固気反応粉末の反応は,容器
内において効率的かつ均一にに進行し,容器に対する応
力の集中も生じない。それ故,本発明にかかる反応容器
は,相対的に小形軽量化することが可能となる。上記の
ように,本発明によれば,固気反応粉末の膨張に伴う応
力の集中を抑制し,反応の進行と熱交換を効率的に行う
ことの出来る小形で高性能の反応容器を提供することが
できる。
As a result, the reaction of the solid-gas reaction powder proceeds efficiently and uniformly in the container, and no concentration of stress on the container occurs. Therefore, the reaction vessel according to the present invention can be made relatively small and lightweight. As described above, according to the present invention, there is provided a small, high-performance reaction vessel capable of suppressing the concentration of stress due to expansion of a solid-gas reaction powder and efficiently performing the reaction and exchanging heat. be able to.

【0013】なお,請求項2記載のように,上記仕切り
棚の形状は,横端部を上方に湾曲させ,容器の垂直壁面
に漸次近接するようすることが好ましい(図1,湾曲部
151参照)。このように,湾曲形状とすることによ
り,仕切り棚は湾曲部において撓み易くなり,固気反応
粉末が膨張する方向に撓むことにより膨張力を吸収する
ことができる。そして,本発明の反応容器は,請求項3
記載のように,水素吸蔵合金の水素吸蔵,放出反応に極
めて好適である。
It is preferable that the shape of the partition shelf is such that the lateral end is curved upward so as to gradually approach the vertical wall surface of the container (see FIG. 1, curved portion 151). ). As described above, the curved shape allows the partition shelf to be easily bent at the curved portion, and can absorb the expansion force by bending in the direction in which the solid-gas reaction powder expands. And, the reaction vessel of the present invention is characterized by claim 3.
As described, it is extremely suitable for hydrogen storage and release reactions of hydrogen storage alloys.

【0014】[0014]

【発明の実施の形態】BEST MODE FOR CARRYING OUT THE INVENTION

実施形態例1 本例は,固気反応粉末としての水素吸蔵合金(MH)に
反応ガスとしての水素ガスを吸脱させる反応容器であ
る。,図1,図2に示すように,反応容器1は,水素吸
蔵合金81を収容し外殻を形成する容器11と,容器1
1を上下方向に複数の区画に区分すると共に水素吸蔵合
金81を載置し水素ガスを透過することのできる仕切り
棚15と,熱媒を流通させ水素吸蔵合金81と熱交換を
行う伝熱管21と,伝熱管21に装着され水素吸蔵合金
81と熱媒との間の伝熱を促進する伝熱フィン25と,
容器11の内と外との間に反応ガスを導入又は排出させ
るガス管31(図2)と,容器11内の水素がスを透過
させるガス透過性フィルターからなりガス管31と連結
されているガス透過管35とを有している。
Embodiment 1 This embodiment is a reaction vessel in which a hydrogen storage alloy (MH) as a solid-gas reaction powder absorbs and desorbs hydrogen gas as a reaction gas. As shown in FIG. 1 and FIG. 2, a reaction vessel 1 includes a vessel 11 that contains a hydrogen storage alloy 81 and forms an outer shell, and a vessel 1.
1 is divided into a plurality of sections in the vertical direction, and a hydrogen storage alloy 81 is placed on the partition shelf 15 through which hydrogen gas can pass, and a heat transfer tube 21 through which a heat medium flows to exchange heat with the hydrogen storage alloy 81. A heat transfer fin 25 mounted on the heat transfer tube 21 to promote heat transfer between the hydrogen storage alloy 81 and the heat medium;
A gas pipe 31 (FIG. 2) for introducing or discharging a reaction gas between the inside and the outside of the vessel 11 and a gas permeable filter through which hydrogen in the vessel 11 permeates are connected to the gas pipe 31. And a gas permeable tube 35.

【0015】そして,伝熱管21は,仕切り棚15によ
って分けられた各区画内の水素吸蔵合金81に接するよ
う配置されている。また,仕切り棚15は,図1に示す
ように,横端部を上方に湾曲させ,容器11の垂直壁面
111に漸次近接するよう形成されている。以下,それ
ぞれについて説明を補足する。
The heat transfer tubes 21 are arranged so as to be in contact with the hydrogen storage alloy 81 in each section divided by the partition shelf 15. As shown in FIG. 1, the partition shelf 15 is formed such that the lateral end is curved upward and gradually approaches the vertical wall surface 111 of the container 11. The following is a supplementary explanation for each.

【0016】反応容器1は,図1,図2に示すように,
断面形状が正方形に近い方形で奥行き方向に長い箱形の
形状を有する。そして,容器11は,5枚の仕切り棚1
5により上下方向に6つの区画に区分けされている。ま
た,伝熱管21は,各区画内において前後方向に等間隔
で配置され,それぞれの区画における伝熱管21の右端
部は他の区画の端部と接続され,左端部下方3区画の伝
熱管21の端部は熱媒の流入口211(図2)と接続さ
れ,上方3区画の伝熱管21の端部は熱媒の流出口21
2(図2)に接続されている。また,ガス透過管35
は,上部中央と中心部とに奥行き方向に延設されてお
り,それぞれの端部はガス管31に接続されている。
As shown in FIG. 1 and FIG.
It has a box-like shape with a rectangular cross section close to a square and long in the depth direction. And the container 11 has five partition shelves 1
5 are vertically divided into six sections. The heat transfer tubes 21 are arranged at equal intervals in the front-rear direction in each section, and the right end of the heat transfer tube 21 in each section is connected to the end of another section, and the heat transfer tubes 21 in the three sections below the left end. Is connected to the heat medium inlet 211 (FIG. 2), and the ends of the heat transfer tubes 21 in the upper three sections are connected to the heat medium outlet 21.
2 (FIG. 2). In addition, the gas permeable tube 35
Are extended in the depth direction at the upper center and the center, and each end is connected to the gas pipe 31.

【0017】反応容器1を構成する各部材11,21,
25,31は,ガス透過管35及び仕切り棚15を除き
アルミニウム合金からなる。そして,容器11と伝熱管
21とは,アルミ押出し成形により一体構造となってい
る。水素吸蔵合金81は,伝熱管21及び伝熱フィン2
5の周りに充填されている。なお,水素吸蔵合金81
は,容器11の前後の端面または側面に設けた充填口
(図示略)から充填される。また,ガス透過管35及び
仕切り棚15は,ステンレス焼結体により形成されてい
る。
Each member 11, 21, constituting the reaction vessel 1
25 and 31 are made of an aluminum alloy except for the gas permeable tube 35 and the partition shelf 15. And the container 11 and the heat transfer tube 21 have an integral structure by aluminum extrusion molding. The hydrogen storage alloy 81 is composed of the heat transfer tube 21 and the heat transfer fin 2.
5 is filled around. The hydrogen storage alloy 81
Is filled from a filling port (not shown) provided on the front or rear end face or side face of the container 11. Further, the gas permeable tube 35 and the partition shelf 15 are formed of a sintered stainless steel.

【0018】ガス透過管35を構成するガス透過性フィ
ルターは,1μm透過フィルターであり,水素透過性の
仕切り棚15は空隙径10μmで厚さ0.4〜0.5m
mのシートである。上記透過指数の決定は,使用する水
素吸蔵合金の活性化処理後の粒径分布に基づいて決定し
たが,後述する実験に使用した水素吸蔵合金81におい
ては,1〜30μmの範囲においてほぼ同様の結果が得
られている。ガス透過管35は,本例では2本とし水素
吸蔵合金81の充填容積の減少を抑制したが,1本以上
であればよい。
The gas permeable filter constituting the gas permeable tube 35 is a 1 μm permeable filter, and the hydrogen permeable partition shelf 15 has a gap diameter of 10 μm and a thickness of 0.4 to 0.5 m.
m. The above-mentioned permeation index was determined on the basis of the particle size distribution of the hydrogen storage alloy used after the activation treatment. However, in the case of the hydrogen storage alloy 81 used in the experiments described later, almost the same was observed in the range of 1 to 30 μm. The results have been obtained. In this example, the number of the gas permeation tubes 35 is two, and the decrease in the filling volume of the hydrogen storage alloy 81 is suppressed.

【0019】伝熱フィン25は,肉厚0.25mmのア
ルミニウムシートを容器の長手方向に積層したものであ
り,伝熱管21にロウづけされている。そして,水素吸
蔵合金81は,各区画に均一に充填され,水素吸蔵合金
の充填量は,粉体工学で一般的に採用されているタップ
密度を基準とした。なお,水素吸蔵合金のタップ密度
は,水素吸蔵合金の活性化前と活性化後とで変化する
が,容器に収容する水素吸蔵合金81の充填率(充填密
度/真密度)は,活性化前のタップ密度と活性化後のタ
ップ密度の間で選択することが好ましい。
The heat transfer fins 25 are formed by laminating aluminum sheets having a thickness of 0.25 mm in the longitudinal direction of the container, and are brazed to the heat transfer tubes 21. The hydrogen storage alloy 81 is uniformly filled in each section, and the filling amount of the hydrogen storage alloy is based on the tap density generally used in powder engineering. Although the tap density of the hydrogen storage alloy changes before and after activation of the hydrogen storage alloy, the filling rate (filling density / true density) of the hydrogen storage alloy 81 contained in the container is determined before activation. It is preferable to select between the tap density after activation and the tap density after activation.

【0020】本例の反応容器1では,活性化後の水素吸
蔵合金のタップ密度の110%程度に充填率(充填密度
/真密度)を大きくしても,反応容器1に過大な応力の
発生は,認められず,また容器内部での水素ガスの透過
性も良好な結果が得られている。しかしながら,水素吸
蔵合金81の充填率を,活性化前のタップ密度まで上昇
させた場合には,本例の反応容器1が破損することは無
かったが,内部における水素ガスの透過性が低下する傾
向が見られた。そのため,水素吸蔵合金の充填率(充填
密度/真密度)は,活性化前のタップ密度以下に設定す
ることが好ましいと思われる。
In the reaction vessel 1 of this embodiment, even if the filling rate (filling density / true density) is increased to about 110% of the tap density of the activated hydrogen storage alloy, excessive stress is generated in the reaction vessel 1. Was not observed, and good results were also obtained for the permeability of hydrogen gas inside the container. However, when the filling rate of the hydrogen storage alloy 81 was increased to the tap density before activation, the reaction vessel 1 of this example was not damaged, but the permeability of hydrogen gas in the interior was reduced. A trend was seen. Therefore, it seems that it is preferable to set the filling rate (filling density / true density) of the hydrogen storage alloy to be equal to or less than the tap density before activation.

【0021】反応容器1に収容された水素吸蔵合金81
は,始めに活性化(水素化)処理が行われる。即ち,加
熱脱気と水素加圧とを繰り返し,水素吸蔵合金が水素ガ
スを吸蔵できるようにし,この過程で水素吸蔵合金は水
素ガスの進入により微粉化する。前記のように,内部が
区画に分けられていない従来の反応容器では,この過程
において微粉化した水素吸蔵合金が容器の下方に偏在
し,活性化初期に発生する大きな膨張力により水素吸蔵
合金が圧密化し,その結果過大な応力の集中が生じてい
た。
Hydrogen storage alloy 81 stored in reaction vessel 1
First, an activation (hydrogenation) process is performed. That is, heat degassing and hydrogen pressurization are repeated so that the hydrogen storage alloy can store hydrogen gas, and in this process, the hydrogen storage alloy is pulverized by the entry of hydrogen gas. As described above, in the conventional reaction vessel in which the interior is not divided into compartments, in this process, the finely divided hydrogen storage alloy is unevenly distributed below the vessel, and the large expansion force generated in the early stage of the activation causes the hydrogen storage alloy to become inactive. The consolidation resulted in excessive stress concentration.

【0022】しかしながら,本例では,仕切り棚15に
より内部空間が6つの区画に区分けされているから,水
素吸蔵合金81は下方に集まることなく分散配置され,
水素吸蔵合金の圧密化は回避される。そして,水素ガス
の拡散はスムースに行われるようになる。次に,水素吸
蔵合金を活性化した後における本例の反応容器1におけ
る応力発生状況と水素ガスの流入流出速度の結果を,従
来の反応容器と比較して示す。なお,従来の反応容器の
場合には,応力の集中が予測されるため,比較に用いた
反応容器は,安全が高くより強度の大きい円筒形の容器
(図11)を採用し,それぞれの反応容器1,9の内容
積はぼ同一とした。
However, in this embodiment, since the internal space is divided into six sections by the partition shelf 15, the hydrogen storage alloys 81 are dispersed and arranged without gathering downward.
Consolidation of the hydrogen storage alloy is avoided. Then, the diffusion of the hydrogen gas is performed smoothly. Next, the state of stress generation and the results of hydrogen gas inflow and outflow velocities in the reaction vessel 1 of this example after activating the hydrogen storage alloy are shown in comparison with those of the conventional reaction vessel. In the case of the conventional reaction vessel, stress concentration is expected. Therefore, the reaction vessel used for comparison is a cylindrical vessel (Fig. 11) that is safe and has higher strength. The inner volumes of the containers 1 and 9 were almost the same.

【0023】始めに,応力の発生状況の測定結果を示
す。応力の発生状況の測定は,水素吸蔵合金から水素を
全量放出させ,その後約250リットル/minの速度
で水素ガスを吸蔵させ,その時の容器11の表面の歪み
の大きさを測定した。図3は,水素吸蔵合金に対する吸
蔵水素量(H/M)の増加に対して,容器にかかる最大
応力と水素ガスのガス圧による応力との比R1がどのよ
うに変化したかを示すものである。
First, the results of measurement of the state of occurrence of stress will be described. For the measurement of the stress generation state, the entire amount of hydrogen was released from the hydrogen storage alloy, and then hydrogen gas was stored at a rate of about 250 liter / min, and the magnitude of the strain on the surface of the container 11 at that time was measured. FIG. 3 shows how the ratio R1 between the maximum stress applied to the container and the stress due to the gas pressure of hydrogen gas changes with the increase in the amount of stored hydrogen (H / M) for the hydrogen storage alloy. is there.

【0024】最大応力とガス圧応力の比R1が1である
ことは,水素吸蔵合金の膨張による応力が容器11に発
生していないことを示す。また,図3の曲線61は,本
例の反応装置1を用い水素吸蔵合金81の充填率を50
%とした場合を示し,曲線951,952は図11に示
す反応容器9において水素吸蔵合金の充填率を40%と
した場合と充填率を48%とした場合を示している。
The fact that the ratio R1 between the maximum stress and the gas pressure stress is 1 indicates that no stress is generated in the container 11 due to the expansion of the hydrogen storage alloy. The curve 61 in FIG. 3 indicates that the filling rate of the hydrogen storage alloy 81 was 50% using the reactor 1 of this example.
%, And curves 951 and 952 show a case where the filling rate of the hydrogen storage alloy is set to 40% and a case where the filling rate is set to 48% in the reaction vessel 9 shown in FIG.

【0025】同図から分かるように,本例の反応容器1
の場合(曲線61)には,吸蔵水素量(H/M)の増加
に対して最大応力とガス圧応力の比R1は大きく変化せ
ず上記比R1が1前後であるのに対して,従来装置を用
いて水素吸蔵合金の充填率をほぼ同じ48%とした場合
(曲線962)には,上記比R1が大幅に上昇し8倍を
越えてしまう(なお,H/Mが0.8以下でデータ採取
を完了したのは,後述する図4に示すように,容器の耐
力限界に近づいて来たためである)。また,曲線951
が示すように,従来装置において水素吸蔵合金の充填率
を本例の容器より2割落として40%とした場合にも,
吸蔵水素量(H/M)が多くなると上記比R1が約3倍
に上昇し,本例の反応容器1の2倍以上となる。
As can be seen from the figure, the reaction vessel 1 of this embodiment
In the case of (curve 61), the ratio R1 between the maximum stress and the gas pressure stress does not change significantly with an increase in the amount of stored hydrogen (H / M), and the ratio R1 is about 1, whereas When the filling rate of the hydrogen storage alloy is set to approximately the same 48% using the apparatus (curve 962), the ratio R1 increases significantly and exceeds 8 times (H / M is 0.8 or less). The reason for completing the data collection is that the container is approaching the proof stress limit as shown in FIG. Also, curve 951
As shown in the figure, even when the filling rate of the hydrogen storage alloy in the conventional apparatus is set at 40%, which is 20% lower than the container of the present example,
When the amount of stored hydrogen (H / M) increases, the ratio R1 increases about three times, and becomes twice or more that of the reaction vessel 1 of this example.

【0026】一方,図4は,水素吸蔵合金に対する吸蔵
水素量(H/M)の増加に対して,容器にかかる最大応
力と容器材料(アルミ合金)の0.2%耐力との比R2
がどのように変化したかを示すものである。そして,図
4の曲線62は,本例の反応装置1を用い水素吸蔵合金
81の充填率を50%とした場合を示し,曲線961,
962は図11に示す反応容器9において水素吸蔵合金
の充填率を40%とした場合と充填率を48%とした場
合を示している。
On the other hand, FIG. 4 shows a ratio R2 between the maximum stress applied to the container and the 0.2% proof stress of the container material (aluminum alloy) with respect to the increase in the amount of stored hydrogen (H / M) with respect to the hydrogen storage alloy.
Shows how has changed. 4 shows a case where the filling rate of the hydrogen storage alloy 81 is set to 50% using the reactor 1 of the present example, and a curve 961,
Reference numeral 962 denotes a case where the filling rate of the hydrogen storage alloy is set to 40% and a case where the filling rate is set to 48% in the reaction vessel 9 shown in FIG.

【0027】曲線62から分かるように,本例の反応容
器1の場合には,0.2%耐力との比R2は,吸蔵水素
量(H/M)が多い領域で若干の増加が見られるだけで
あり,この増加は,水素吸蔵合金の平衡圧力が上昇する
領域に相当し内部の水素ガス圧の上昇によるものであ
る。一方,曲線962が示すように,従来装置を用いて
水素吸蔵合金の充填率を本例の容器とほぼ同じ48%と
した場合には,上記比R2が大幅に上昇しH/M比0.
7以上で0.2%耐力を越える結果が得られている。
As can be seen from the curve 62, in the case of the reaction vessel 1 of the present example, the ratio R2 with respect to the 0.2% proof stress slightly increases in a region where the amount of stored hydrogen (H / M) is large. This increase corresponds to a region where the equilibrium pressure of the hydrogen storage alloy increases and is due to an increase in the internal hydrogen gas pressure. On the other hand, as shown by the curve 962, when the filling rate of the hydrogen storage alloy is set to 48%, which is almost the same as that of the container of the present example, using the conventional apparatus, the above ratio R2 greatly increases, and the H / M ratio becomes 0.1%.
A result exceeding 0.2% proof stress is obtained at 7 or more.

【0028】また,曲線961が示すように,従来装置
において水素吸蔵合金の充填率を本例の容器より2割落
として40%とした場合にも,吸蔵水素量(H/M)が
多くなると上記比R2が大幅に上昇する。上記結果は,
本例の反応容器1を用いることにより,大幅に小形にし
て同じ量の水素吸蔵合金の反応を処理可能なことを示し
ている。
Further, as shown by the curve 961, even when the filling rate of the hydrogen storage alloy in the conventional apparatus is set to 40%, which is 20% lower than that of the container of this embodiment, the hydrogen storage amount (H / M) increases. The above ratio R2 greatly increases. The above result is
It is shown that the use of the reaction vessel 1 of this example makes it possible to treat the reaction of the same amount of hydrogen storage alloy in a significantly smaller size.

【0029】次に,反応容器1,9の水素透過性能の評
価結果を示す。水素透過性能の評価は,反応容器に流入
流出する水素流量を指標とした(伝熱フィンのフィンピ
ッチは両容器とも2mmで同一)。図5は水素吸蔵時に
おける水素流量(水素吸蔵合金の単位重量当たりの水素
流量リットル/min)を示し,図6は水素放出時にお
ける水素流量(水素吸蔵合金の単位重量当たりの水素流
量リットル/min)を示すものである。水素吸蔵時の
測定は,初期の吸蔵水素量H/Mを0.3とし,伝熱管
21に流入させる熱媒の温度を35℃一定とし,水素ガ
スの圧力は35℃の水素吸蔵合金の平衡圧力に対して
0.3MPa高い一定の値とした。
Next, the evaluation results of the hydrogen permeation performance of the reaction vessels 1 and 9 will be shown. The hydrogen permeation performance was evaluated by using the flow rate of hydrogen flowing into and out of the reaction vessel as an index (the fin pitch of the heat transfer fins was 2 mm in both vessels and was the same). FIG. 5 shows the hydrogen flow rate during storage of hydrogen (hydrogen flow rate per unit weight of hydrogen storage alloy in liter / min), and FIG. 6 shows the hydrogen flow during hydrogen release (hydrogen flow rate per unit weight of hydrogen storage alloy in liter / min). ). In the measurement at the time of hydrogen storage, the initial amount of stored hydrogen H / M was 0.3, the temperature of the heating medium flowing into the heat transfer tube 21 was fixed at 35 ° C., and the pressure of the hydrogen gas was 35 ° C. The pressure was set to a constant value 0.3 MPa higher than the pressure.

【0030】図5の曲線97は,従来の反応容器9にお
ける水素吸蔵合金の単位重量当たりの水素流量を示し,
曲線63は本例の水素流量を示す。同図から分かるよう
に,本例の反応容器1は従来容器に比べて極めて良好な
水素吸蔵特性を示す。これは,従来装置では,容器内部
における水素拡散が不十分であり,ガス透過管35の近
傍の水素吸蔵合金では良好な水素吸蔵が行われるがガス
透過管35から遠い場所の水素吸蔵合金では水素ガスが
到達せず,吸蔵が少ないことを示すものである。その結
果,流入する水素ガス流量は,大幅に少なくなる。
A curve 97 in FIG. 5 shows a hydrogen flow rate per unit weight of the hydrogen storage alloy in the conventional reaction vessel 9.
Curve 63 shows the hydrogen flow rate of this example. As can be seen from the figure, the reaction vessel 1 of the present example exhibits extremely good hydrogen storage characteristics as compared with the conventional vessel. This is because in the conventional apparatus, hydrogen diffusion inside the container is insufficient, and the hydrogen storage alloy near the gas permeation pipe 35 performs good hydrogen storage, but the hydrogen storage alloy far from the gas permeation pipe 35 does not. This indicates that the gas did not reach and the occlusion was small. As a result, the flow rate of the flowing hydrogen gas is significantly reduced.

【0031】一方,本例では,容器内部を区分けし,水
素吸蔵合金の分布を均一化しているため,全域での水素
ガスの透過拡散性が良好となる。また,前記のように,
水素吸蔵合金の圧密化が生じないため,圧密化による水
素ガスの拡散阻害も生じない。なお,時間の経過ととも
に両曲線63,97の流量の差は小さくなるが,それは
吸蔵可能水素量が同一量であるためである。
On the other hand, in this embodiment, since the inside of the container is divided and the distribution of the hydrogen storage alloy is made uniform, the hydrogen gas permeation / diffusion is improved over the entire region. Also, as mentioned above,
Since the compaction of the hydrogen storage alloy does not occur, the diffusion of hydrogen gas is not hindered by the compaction. It should be noted that the difference between the flow rates of the curves 63 and 97 becomes smaller with the passage of time because the amount of storable hydrogen is the same.

【0032】一方,図6に示す水素ガス放出時の測定条
件は,初期の吸蔵水素量(H/M)を0.7に設定し,
伝熱管21に流入させる熱媒の温度を10℃一定とし,
水素ガスは,大気圧中に放出させた。図6の曲線98
は,従来装置における水素吸蔵合金の単位重量当たりの
水素流量を示し,曲線64は本例の水素流量を示す。
On the other hand, the measurement conditions at the time of releasing hydrogen gas shown in FIG. 6 are as follows: the initial amount of stored hydrogen (H / M) is set to 0.7;
The temperature of the heat medium flowing into the heat transfer tube 21 is kept constant at 10 ° C.
Hydrogen gas was released into the atmosphere. Curve 98 in FIG.
Indicates the hydrogen flow rate per unit weight of the hydrogen storage alloy in the conventional device, and curve 64 indicates the hydrogen flow rate in this example.

【0033】水素放出の場合には,開始直後にには容器
内部の圧力に対応して容器の内部に存在する水素ガスが
放出されるため,両曲線64,98間に大きな差がない
が,時間の経過と共に新たに水素吸蔵合金から放出され
る水素が主体となり,両装置における水素透過性の差が
流出ガス流量の差として徐々に表れてくる。なお,水素
吸蔵時よりも両者の差が少ないのは,水素放出時には水
素吸蔵合金が収縮するため従来装置の場合にも水素ガス
の拡散は比較的容易となるためと思われる。
In the case of hydrogen release, immediately after the start, hydrogen gas existing inside the container is released in accordance with the pressure inside the container, so that there is no large difference between the curves 64 and 98. With the passage of time, hydrogen newly released from the hydrogen storage alloy becomes the main component, and the difference in hydrogen permeability between the two devices gradually appears as the difference in the outflow gas flow rate. The reason why the difference between the two is smaller than that during hydrogen storage is considered to be that diffusion of hydrogen gas is relatively easy even in the case of the conventional apparatus because the hydrogen storage alloy shrinks during hydrogen release.

【0034】上記のように,本例の反応容器1によれ
ば,水素ガスの透過性が良好であり,水素ガスの流入流
出速度を大きくすることができるから,反応容器1から
得られる熱出力を大きくすることができる。また,容器
内部における水素透過性が良好であることから,内部で
の反応がほぼ均一かつ連続的にに進行するため,モデル
化による数値解析が容易となり,例えば伝熱管や伝熱フ
ィンの最適化設計が容易となる。何故ならば,従来装置
のように,水素吸蔵合金に圧密化が生じ,例えばガス流
通路に閉塞部等が形成されると,数値解析が困難とな
り,また使用したモデルとの乖離が大きくなるからであ
る。
As described above, according to the reaction vessel 1 of the present embodiment, since the hydrogen gas permeability is good and the flow rate of the hydrogen gas can be increased, the heat output obtained from the reaction vessel 1 can be increased. Can be increased. In addition, because the hydrogen permeability inside the vessel is good, the reaction inside the vessel proceeds almost uniformly and continuously, so that numerical analysis by modeling is easy, for example, optimization of heat transfer tubes and heat transfer fins Design becomes easy. This is because, as in the conventional device, when the hydrogen storage alloy is compacted and, for example, an obstruction is formed in the gas flow passage, numerical analysis becomes difficult and the deviation from the model used increases. It is.

【0035】また,反応容器の強度設計の場合にも,応
力の集中,偏在がないことから,内部のガス圧に対する
強度を中心にした設計が可能となり,設計が容易である
と共に,容器の強度を低く設定することが可能となる。
即ち,応力の集中を考慮しなければならない場合には,
その予測が困難であることから,経験等に基づき安全サ
イドに強度を設定することになるからである。
Also, in the case of the strength design of the reaction vessel, since there is no concentration and uneven distribution of stress, it is possible to design the strength mainly with respect to the internal gas pressure. Can be set low.
That is, when the concentration of stress must be considered,
This is because the prediction is difficult, and the strength is set on the safe side based on experience and the like.

【0036】更に,本例の仕切り棚15は,図1に示す
ように,横端部を上方に湾曲させた湾曲部151を設け
てあり,湾曲部151が撓むことにより水素吸蔵合金の
膨張による応力を分担することができる。また,湾曲に
よる水素透過面積の増加により水素ガスの透過を容易に
することができる。上記のように,本例の反応容器1に
よれば,小形にして同様の性能を得ることができ,同様
の大きさではより優れた性能を発揮することができる。
Further, as shown in FIG. 1, the partition shelf 15 of this embodiment is provided with a curved portion 151 having a lateral end curved upward, and the curved portion 151 is bent to expand the hydrogen storage alloy. Can be shared. In addition, the permeation of hydrogen gas can be facilitated by increasing the hydrogen permeation area due to the curvature. As described above, according to the reaction vessel 1 of the present example, the same performance can be obtained by reducing the size, and more excellent performance can be exhibited with the same size.

【0037】実施形態例2 本例は,図7に示すように,実施形態例1において,容
器11の内壁の全周に沿ってガス透過性のシート16を
配置したもう一つの実施形態例である。本例によれば,
上記シート16がクッションとなり,容器11に加えら
れる水素吸蔵合金81の膨張力を低減することができ,
また,本シート16は仕切り棚15とは異なり水素吸蔵
合金を保持する機能が必要ないことから,空隙径の大き
なものを使用でき,シート16内を水素ガスが容易に流
通可能なため水素ガスの拡散を促進する効果がある。ま
た,シート16は,容器の内外間の断熱層としての効果
がある。その他については実施形態例1と同様である。
Second Embodiment As shown in FIG. 7, this embodiment is another embodiment in which the gas permeable sheet 16 is arranged along the entire circumference of the inner wall of the container 11 in the first embodiment. is there. According to this example,
The sheet 16 serves as a cushion, and the expansion force of the hydrogen storage alloy 81 added to the container 11 can be reduced.
Further, unlike the partition shelf 15, the sheet 16 does not require a function of holding the hydrogen storage alloy, so that a sheet having a large void diameter can be used. It has the effect of promoting diffusion. Further, the sheet 16 has an effect as a heat insulating layer between the inside and the outside of the container. Others are the same as the first embodiment.

【0038】実施形態例3 本例は,図8に示すように,実施形態例1において,伝
熱管21の周囲の伝熱フィン26をスパイラル状とした
もう一つの実施形態例である。即ち,伝熱フィン26
は,図9に示すように,伝熱管21の周囲にスパイラル
状に形成されている。その結果,水素吸蔵合金が伝熱フ
ィン26に沿って長手方向に,重力あるいは振動を加え
ることで移動可能であるから,水素吸蔵合金を充填する
のが容易となる。
Third Embodiment As shown in FIG. 8, this embodiment is another embodiment in which the heat transfer fins 26 around the heat transfer tube 21 in the first embodiment are spirally formed. That is, the heat transfer fins 26
Are formed in a spiral shape around the heat transfer tube 21 as shown in FIG. As a result, the hydrogen storage alloy can be moved in the longitudinal direction along the heat transfer fins 26 by applying gravity or vibration, so that the hydrogen storage alloy can be easily filled.

【0039】伝熱フィン26は,実施形態例1の伝熱フ
ィン25よりも放熱面積が小さいことから,熱交換性能
は劣るが水素吸蔵合金81をより多く充填することが可
能である。その他については実施形態例1と同様であ
る。
Since the heat transfer fin 26 has a smaller heat radiation area than the heat transfer fin 25 of the first embodiment, the heat transfer fin 26 is inferior in heat exchange performance, but can be filled with the hydrogen storage alloy 81 more. Others are the same as the first embodiment.

【0040】実施形態例4 本例は,実施形態例1から実施形態例3において,仕切
り棚15におけるガス透過用の細孔の大きさを場所毎に
変化させるようにしたもう一つの実施形態例である。即
ち,下の段の仕切り棚15ほど細孔の径を大きく且つ粗
くし,上の仕切り棚15ほど細孔の径を小さく且つ密に
する。
Fourth Embodiment This embodiment is another embodiment in which the size of the gas permeation pores in the partitioning shelf 15 is changed for each location in the first to third embodiments. It is. In other words, the diameter of the pores is made larger and coarser as the partition 15 is lower, and the diameter of the pores is made smaller and denser as the partition 15 is upper.

【0041】その結果,容器11の下方の仕切り棚15
の水素透過性が良好となり,ガス透過管35との距離の
差による水素ガスの回収または浸透の差がなくなり,容
器11内の場所によらず均一に水素吸蔵合金の反応を促
進することができる。その他,については,実施形態例
1〜実施形態例3と同様である。
As a result, the partition shelf 15 below the container 11
Has a good hydrogen permeability, and there is no difference in the recovery or permeation of hydrogen gas due to the difference in the distance from the gas permeable pipe 35, and the reaction of the hydrogen storage alloy can be promoted uniformly regardless of the location in the container 11. . Others are the same as those of the first to third embodiments.

【0042】実施形態例5 本例は,図10に示すように,実施形態例1において,
水素吸蔵合金81を収容する区画のうちガス透過管35
の存在する最上段の区画41の上下幅L1を他の区画の
上下幅L2よりも大きくしたもう一つの実施形態例であ
る。本例によれば,各区画の水素吸蔵合金81は,自重
により区画の下の方に集まり易いから,ガス透過管35
の存在する区画41(最上段)の上部に水素ガス流通路
が形成される。そのため,ガス透過管35に加えて上記
水素ガス流通路によって容器全体に水素ガスの拡散が可
能であるから,全体の水素ガスの拡散性が向上する。そ
の他については実施形態例1と同様である。
Fifth Embodiment As shown in FIG. 10, this embodiment is different from the first embodiment in that
The gas permeable pipe 35 of the compartment containing the hydrogen storage alloy 81
This is another embodiment in which the upper and lower widths L1 of the uppermost section 41 in which is present are larger than the upper and lower widths L2 of the other sections. According to this example, the hydrogen storage alloy 81 in each section is likely to gather below the section due to its own weight.
A hydrogen gas flow passage is formed in the upper part of the section 41 (the uppermost stage) in which is present. For this reason, the hydrogen gas can be diffused to the entire vessel by the hydrogen gas flow passage in addition to the gas permeable pipe 35, so that the diffusivity of the entire hydrogen gas is improved. Others are the same as the first embodiment.

【0043】[0043]

【発明の効果】上記のように,本発明によれば,固気反
応粉末の膨張に伴う応力の集中を抑制し,反応の進行と
熱交換を効率的に行うことの出来る小形で高性能の反応
容器を得ることができる。
As described above, according to the present invention, it is possible to suppress the concentration of stress accompanying the expansion of the solid-gas reaction powder, and to achieve a small, high-performance device capable of efficiently conducting the reaction and exchanging heat. A reaction vessel can be obtained.

【0044】[0044]

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

【図1】実施形態例1の水素吸蔵合金の反応容器の正面
断面図。
FIG. 1 is a front sectional view of a hydrogen storage alloy reaction container according to a first embodiment.

【図2】図1のA−A矢視線断面図。FIG. 2 is a sectional view taken along line AA of FIG.

【図3】実施形態例1の反応容器における吸蔵水素量
(H/M)と,容器にかかる最大応力のガス圧力に対す
る比R1との関係を従来装置と比較して示した図。
FIG. 3 is a diagram showing the relationship between the amount of stored hydrogen (H / M) in the reaction vessel of Embodiment 1 and the ratio R1 of the maximum stress applied to the vessel to the gas pressure in comparison with a conventional apparatus.

【図4】実施形態例1の反応容器における吸蔵水素量
(H/M)と,容器にかかる最大応力の容器の0.2%
耐力に対する比R2との関係を従来装置と比較して示し
た図。
FIG. 4 shows the amount of stored hydrogen (H / M) in the reaction vessel of Embodiment 1 and 0.2% of the maximum stress applied to the vessel.
The figure which showed the relationship with the ratio R2 with respect to proof stress compared with the conventional apparatus.

【図5】実施形態例1の反応容器における水素吸蔵合金
の単位重量当たりの吸蔵水素流量の時間変化を従来装置
と比較して示した図。
FIG. 5 is a diagram showing a time change of a flow rate of stored hydrogen per unit weight of a hydrogen storage alloy in a reaction vessel of Embodiment 1 in comparison with a conventional apparatus.

【図6】実施形態例1の反応容器における水素吸蔵合金
の単位重量当たりの放出水素流量の時間変化を従来装置
と比較して示した図。
FIG. 6 is a diagram showing a change over time of a flow rate of released hydrogen per unit weight of the hydrogen storage alloy in the reaction vessel of Embodiment 1 in comparison with a conventional apparatus.

【図7】実施形態例2の水素吸蔵合金の反応容器の正面
断面図。
FIG. 7 is a front sectional view of a hydrogen storage alloy reaction container according to a second embodiment.

【図8】実施形態例3の水素吸蔵合金の反応容器の正面
断面図。
FIG. 8 is a front sectional view of a hydrogen storage alloy reaction container according to a third embodiment.

【図9】実施形態例3の伝熱フィンを伝熱管に装着した
状態を示す部分拡大図。
FIG. 9 is a partially enlarged view showing a state in which the heat transfer fin according to the third embodiment is mounted on a heat transfer tube.

【図10】実施形態例5の水素吸蔵合金の反応容器の正
面断面図。
FIG. 10 is a front sectional view of a hydrogen storage alloy reaction container according to a fifth embodiment.

【図11】従来の水素吸蔵合金の反応容器の正面断面
図。
FIG. 11 is a front sectional view of a conventional hydrogen storage alloy reaction vessel.

【符号の説明】[Explanation of symbols]

1...反応容器, 11...容器, 15...仕切り棚, 21...伝熱管, 25,26...伝熱フィン, 35...ガス透過管, 81...水素吸蔵合金(固気反応粉末), 1. . . 10. reaction vessel, . . Container, 15. . . Partition shelf, 21. . . Heat transfer tubes, 25, 26. . . Heat transfer fins, 35. . . Gas permeation tube, 81. . . Hydrogen storage alloy (solid-gas reaction powder),

───────────────────────────────────────────────────── フロントページの続き (72)発明者 三井 宏之 愛知県愛知郡長久手町大字長湫字横道41番 地の1 株式会社豊田中央研究所内 (72)発明者 青木 博史 愛知県愛知郡長久手町大字長湫字横道41番 地の1 株式会社豊田中央研究所内 (72)発明者 久保 秀人 愛知県刈谷市豊田町2丁目1番地 株式会 社豊田自動織機製作所内 (72)発明者 藤 敬司 愛知県刈谷市豊田町2丁目1番地 株式会 社豊田自動織機製作所内 (72)発明者 藤田 信雄 愛知県豊田市トヨタ町1番地 トヨタ自動 車株式会社内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Hiroyuki Mitsui 41, Yokomichi, Yokomichi, Nagakute-cho, Aichi-gun, Aichi Prefecture Inside Toyota Central R & D Laboratories Co., Ltd. 41 No. 1 Yokomichi, Toyota Central Research Institute, Inc. (72) Inventor Hideto Kubo 2-1-1, Toyota-cho, Kariya-shi, Aichi Prefecture Inside Toyota Industries Corporation (72) Inventor Keiji Fuji, Kariya-shi, Aichi Prefecture 2-1-1 Toyota Town Inside Toyota Industries Corporation (72) Inventor Nobuo Fujita 1-1 Toyota Town Toyota City, Aichi Prefecture Inside Toyota Motor Corporation

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 固気反応粉末に反応ガスを吸脱させる反
応容器であって,固気反応粉末を収容し外殻を形成する
容器と,容器を上下方向に複数の区画に区分すると共に
上記固気反応粉末を載置し反応ガスを透過することので
きる仕切り棚と,熱媒を流通させ上記固気反応粉末と熱
交換を行う伝熱管と,この伝熱管に装着され固気反応粉
末と熱媒との間の伝熱を促進する伝熱フィンと,上記容
器の内と外との間に反応ガスを導入又は排出させるガス
管と,容器内の反応ガスを透過させ上記ガス管と連結さ
れているガス透過管とを有しており,上記伝熱管は,上
記仕切り棚によって分けられた各区画内の固気反応粉末
に接するよう配置されていることを特徴とする固気反応
粉末の反応容器。
1. A reaction container for absorbing and desorbing a reaction gas into a gas-solid reaction powder, the container containing the gas-solid reaction powder and forming an outer shell, and the container is vertically divided into a plurality of sections. A partition shelf on which the solid-gas reaction powder is placed and through which the reaction gas can pass, a heat transfer tube through which a heat medium flows to exchange heat with the solid-gas reaction powder, and a solid-gas reaction powder attached to the heat transfer tube. A heat transfer fin for promoting heat transfer between the heating medium, a gas pipe for introducing or discharging a reaction gas between the inside and the outside of the vessel, and a connection with the gas pipe for allowing the reaction gas in the vessel to pass therethrough Wherein the heat transfer tube is disposed in contact with the solid-gas reaction powder in each section divided by the partition shelf. Reaction vessel.
【請求項2】 請求項1において,前記仕切り棚は,横
端部を上方に湾曲させ,容器の垂直壁面に漸次近接する
よう形成されていることを特徴とする固気反応粉末の反
応容器。
2. A reaction vessel for solid-gas reaction powder according to claim 1, wherein the partition shelf has a lateral end curved upward and is formed so as to gradually approach a vertical wall surface of the vessel.
【請求項3】 請求項1または請求項2において,前記
固気反応粉末は水素吸蔵合金であり,反応ガスは水素ガ
スであることを特徴とする水素吸蔵合金の反応容器。
3. The hydrogen storage alloy reaction vessel according to claim 1, wherein the solid-gas reaction powder is a hydrogen storage alloy, and the reaction gas is a hydrogen gas.
JP26250296A 1996-09-10 1996-09-10 Reaction vessel for solid gas reaction powder Expired - Fee Related JP3640476B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26250296A JP3640476B2 (en) 1996-09-10 1996-09-10 Reaction vessel for solid gas reaction powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26250296A JP3640476B2 (en) 1996-09-10 1996-09-10 Reaction vessel for solid gas reaction powder

Publications (2)

Publication Number Publication Date
JPH1085582A true JPH1085582A (en) 1998-04-07
JP3640476B2 JP3640476B2 (en) 2005-04-20

Family

ID=17376701

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3640476B2 (en)

Also Published As

Publication number Publication date
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