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
JPS591934B2 - Automatic control method of heat storage/dissipation system using metal hydrides - Google Patents
[go: Go Back, main page]

JPS591934B2 - Automatic control method of heat storage/dissipation system using metal hydrides - Google Patents

Automatic control method of heat storage/dissipation system using metal hydrides

Info

Publication number
JPS591934B2
JPS591934B2 JP55150823A JP15082380A JPS591934B2 JP S591934 B2 JPS591934 B2 JP S591934B2 JP 55150823 A JP55150823 A JP 55150823A JP 15082380 A JP15082380 A JP 15082380A JP S591934 B2 JPS591934 B2 JP S591934B2
Authority
JP
Japan
Prior art keywords
hydrogen gas
heat
pressure
holder
flow rate
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
JP55150823A
Other languages
Japanese (ja)
Other versions
JPS5774592A (en
Inventor
啓介 植田
祥 金沢
寿 樋高
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.)
Kawasaki Heavy Industries Ltd
Original Assignee
Kawasaki Heavy Industries 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 Kawasaki Heavy Industries Ltd filed Critical Kawasaki Heavy Industries Ltd
Priority to JP55150823A priority Critical patent/JPS591934B2/en
Publication of JPS5774592A publication Critical patent/JPS5774592A/en
Publication of JPS591934B2 publication Critical patent/JPS591934B2/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
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/14Thermal energy storage

Landscapes

  • Filling Or Discharging Of Gas Storage Vessels (AREA)

Description

【発明の詳細な説明】 この発明は、金属水素化物の水素吸、脱蔵の際の生成熱
を利用する蓄、放熱システムの自動コントロール方法に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an automatic control method for a heat storage and heat release system that utilizes the heat generated during hydrogen absorption and devolatilization of metal hydrides.

一般に水素貯蔵金属と称する。Generally called hydrogen storage metal.

ランタニド(Lanthanide、希土類)アクチニ
ド(Actinide)元素を含めて、周期律表第3〜
第5周期の遷位金属元素、又はそれらの元素を含む合金
例えばTiFe等は、ある温度、圧力条件のもとで大量
の水素ガスを吸蔵して金属水素化物を作わ易く、その過
程では発熱し、別のある温度、圧力条件のもとで水素を
脱蔵し、その過程では吸熱することが知られている。
Including the lanthanide (rare earth) and actinide elements, elements from periodic table 3 to
Transition metal elements in the fifth period, or alloys containing these elements, such as TiFe, easily absorb a large amount of hydrogen gas under certain temperature and pressure conditions to form metal hydrides, and in the process they generate heat. However, it is known that hydrogen is devolatilized under certain temperature and pressure conditions, and that it absorbs heat in the process.

水素貯蔵金属の上述の特性を利用することにより、金属
水素化物を蓄熱体に使つて、太陽熱、風力等の自然玉子
ルギーや工業廃熱等を蓄熱し、必要に応じてその熱を取
出して例えば僻地の菜園の温室暖房等に利用する蓄・放
熱システムの研究が活発になつてきた。
By utilizing the above-mentioned properties of hydrogen storage metals, metal hydrides can be used as heat storage bodies to store natural energy such as solar heat, wind power, industrial waste heat, etc., and extract the heat as needed, for example. Research into heat storage and radiation systems for use in heating greenhouses in vegetable gardens in remote areas has become active.

金属水素化物を保持して、これに水素ガスホルダーより
供給された水素ガスを接触させて水素を吸蔵させ、その
際発生する熱を取出し、外部より熱を与えて該金属に蓄
熱させ、その際脱蔵された水素ガスを水素ガスホルダー
に戻す熱交換器は反応槽と伝われる。
A metal hydride is held, hydrogen gas supplied from a hydrogen gas holder is brought into contact with the metal hydride, hydrogen is absorbed, the heat generated at that time is extracted, heat is given from the outside and the metal is stored, and at that time A heat exchanger that returns the devolatilized hydrogen gas to the hydrogen gas holder is called a reaction tank.

反応槽は上記目的に対し、金属水素化物の粒子を保持す
るスペースと、該スペースに保持された金属水素化物に
水素ガスを供給し、脱蔵された水素ガスを回収するため
の通気性壁を介して上記金属保持スペースに接する水素
ガス保持スペースと、吸、脱蔵時の反応熱を取出すため
に上記金属保持スペース内に配設した熱交換管又は該ス
ペースの壁面としての熱交換面を有し、吸。脱蔵時の反
応熱は上記熱交管又は熱交換面を介して熱交換流体によ
り回収する。又水素ガス保持スペースは水素ガス配管を
介して水素ガスホルダーに接続されている。金属水素化
物の特長の一つとして、水素ガスの吸・脱蔵の速いこと
が挙げられるが、それは熱玉不ルギーの貯蔵と均一な利
用を目的とした蓄。
For the above purpose, the reaction tank has a space for holding metal hydride particles and a permeable wall for supplying hydrogen gas to the metal hydride held in the space and recovering the devolatilized hydrogen gas. A hydrogen gas holding space in contact with the metal holding space through the metal holding space, and a heat exchange pipe disposed within the metal holding space or a heat exchange surface as a wall surface of the space for extracting reaction heat during adsorption and devolatilization. S-suck. The reaction heat during devolatilization is recovered by a heat exchange fluid through the heat exchange tube or heat exchange surface. Further, the hydrogen gas holding space is connected to a hydrogen gas holder via a hydrogen gas pipe. One of the characteristics of metal hydrides is that they absorb and desorb hydrogen gas quickly, and this is because they are used for storage and uniform use of hot metal hydrides.

放熱システムに}いては欠点となる。もし、水素ガスを
金属に吸蔵させる放熱過程時に、何ら制御することなく
水素ガスを金属に与えて吸蔵させると、最初は砂地に水
が吸収される如く多量に吸蔵され、時間の経過と共に吸
蔵量が漸減し飽和して吸蔵が停止する。したがつて、そ
の時に発生する熱を熱交換流体で熱交換して得られる温
度は、第1図に実線で示すように、初期温度T。から急
速に上昇して最高温度Tmaxに達し、その後漸減して
前記T。になつて放熱が完了する。暖房等の使用目的に
対しては、第1図中に破線で示すような、全放熱期間に
わたつてほマ一定の温度Tmの熱が得られることが必要
であるが、そのためには金属に与えられる水素ガスの流
量をコントコールして、金属の吸収する水素ガスの質量
が放熱期間を通じて一定になるようにすることが必要で
ある。金属に供給する水素ガスの流量をコントロールす
るには、水素ガスホルダーと反応槽とを接続する水素ガ
ス配管に流量調節弁を設置して、放熱過程で水素ガスホ
ルダーと反応槽内の水素ガス圧力の差が変化しても常に
一定の質量流量になるように調節することが必要である
。従来、その制御は流量計(質量流量計)を用いて水素
ガスの流量(質量流量)を検出し、その検出値と設定値
との大小を比較して、電気式又は気二体制御式のコント
ローラで流量調節弁を,駆動させるようにしていた。
This is a drawback for heat dissipation systems. If hydrogen gas is applied to the metal without any control during the heat dissipation process to absorb hydrogen gas into the metal, a large amount will be absorbed at first, just like water is absorbed by sand, and as time passes, the amount of hydrogen gas absorbed will increase. gradually decreases and saturates, and storage stops. Therefore, the temperature obtained by exchanging the heat generated at that time with the heat exchange fluid is the initial temperature T, as shown by the solid line in FIG. The temperature rises rapidly from the temperature Tmax to reach the maximum temperature Tmax, and then gradually decreases to the temperature Tmax. heat dissipation is complete. For purposes such as heating, it is necessary to obtain heat at a nearly constant temperature Tm over the entire heat dissipation period, as shown by the broken line in Figure 1. It is necessary to control the flow rate of hydrogen gas provided so that the mass of hydrogen gas absorbed by the metal remains constant throughout the heat dissipation period. To control the flow rate of hydrogen gas supplied to the metal, a flow control valve is installed on the hydrogen gas piping connecting the hydrogen gas holder and the reaction tank, and the hydrogen gas pressure in the hydrogen gas holder and reaction tank is adjusted during the heat dissipation process. It is necessary to adjust the mass flow rate to always maintain a constant mass flow rate even if the difference between the two changes. Conventionally, this control has been carried out by detecting the flow rate (mass flow rate) of hydrogen gas using a flow meter (mass flow meter), comparing the detected value with a set value, and then using an electric or gas control type. The flow control valve was driven by a controller.

したがつて制御用気体源又は電源装置が必要になり、き
らに電気を使用する場合は水素ガスを取扱う関係上防爆
対策が必要になり、装置が複雑になりかつコスト高にな
る欠点がjあつた。この発明は、金属水素化物による蓄
.放熱システムにおける従来の水素ガス流量調節弁の制
御方法の上述の欠点を解消した、簡単な構成で確実に目
的を達成することのできる自動コントロール方一法を提
供することを目的とする。
Therefore, a control gas source or power supply is required, and when using electricity, explosion-proof measures are required because hydrogen gas is handled, which has the disadvantage of complicating the equipment and increasing costs. Ta. This invention provides storage using metal hydrides. It is an object of the present invention to provide an automatic control method that eliminates the above-mentioned drawbacks of the conventional method of controlling a hydrogen gas flow rate control valve in a heat dissipation system and can reliably achieve the objective with a simple configuration.

以下、本発明を、その実施例を示す図面にもとずいて詳
細に説明する。
Hereinafter, the present invention will be explained in detail based on drawings showing embodiments thereof.

さきに説明した金属水素物による蓄.放熱システムに}
いて水素ガスの流量を一定にコントローqルした場合は
、放熱及び蓄熱過程で水素ガスホルダー及び反応槽内の
水素ガスの圧力は第2図に示す如く変化する。
Storage by the metal hydride explained earlier. For heat dissipation system}
When the flow rate of hydrogen gas is controlled to be constant, the pressure of the hydrogen gas in the hydrogen gas holder and reaction tank changes as shown in FIG. 2 during heat radiation and heat storage processes.

第2図の横軸は時間、縦軸は水素ガス圧力を示し、aは
放熱開始時点、bは放熱終了時点及び蓄熱開始時点、c
は蓄熱終了時点を示す。図中実線で示した曲線は水素ガ
スホルダー内水素ガス圧力を、一点鎖線で示した曲線は
反応槽内水素ガス圧力を示す。本発明の制御方法は、放
熱.蓄熱過程に}ける水素ガスホルダー内のこのような
圧力変化を利用して水素ガス流量調節弁の作動をコント
ロールするようにしたことを特徴とする。
In Fig. 2, the horizontal axis shows time, the vertical axis shows hydrogen gas pressure, a is the time when heat radiation starts, b is the time when heat radiation ends and heat storage starts, and c
indicates the end of heat storage. In the figure, the solid line indicates the hydrogen gas pressure in the hydrogen gas holder, and the dashed line indicates the hydrogen gas pressure in the reaction tank. The control method of the present invention includes heat radiation. The present invention is characterized in that the operation of the hydrogen gas flow rate control valve is controlled by utilizing such pressure changes within the hydrogen gas holder during the heat storage process.

第3図は、本発明の制御方法を適用した蓄.放熱システ
ムの配管系統図である。
FIG. 3 shows a storage system to which the control method of the present invention is applied. It is a piping system diagram of a heat radiation system.

図に}いて、水素ガスホルダー1と反応槽8とを繋ぐ水
素ガス配管15,16の間には、流量(質量流量)調節
弁2が設けられている。該流量調節弁2の二ードル弁と
して形成された弁体21を下端に有るを弁棒22は弁箱
23をグランドパツキン24で気密を保持して貫通した
後、その上端はシリンダー3内に摺動可能に配設された
ピストン31に取付けられている。該ピストン31の土
面とシリンダー3の上端内面との間にはベローズ4が設
けられ、ベローズ4内空間41と水素ガスホルダー1と
は管17で連結されている。管17には止弁13が設け
られている。ピストン31の下面とシリンダ3の下端内
面との間には圧縮スプリング5が設けられ、ピストン3
1を上方に押圧している。弁棒22には手動スタート装
置6が取付けられている。反応槽8内には金属水素化物
粒子を保持する通気性壁体で構成された容器12が設け
られ、該容器12内には両端が反応槽外に延びた熱交換
用流体管9が設けられている。又、ベローズ4と止弁1
3の間の水素ガス配管17には、本システムに水素ガス
を充填するため、止弁10及び減圧弁11を有する管1
8を介して水素ガスボンベ7が接続されて於り、また必
要の場合、このシステムより水素ガスを抜き取るため、
止弁14を有する管19が接続されている。
In the figure, a flow rate (mass flow rate) control valve 2 is provided between hydrogen gas pipes 15 and 16 that connect the hydrogen gas holder 1 and the reaction tank 8. The valve body 21 formed as a needle valve of the flow rate control valve 2 is located at the lower end, and the valve stem 22 penetrates the valve body 23 while maintaining airtightness with the gland packing 24, and then the upper end thereof is slid into the cylinder 3. It is attached to a movably arranged piston 31. A bellows 4 is provided between the ground surface of the piston 31 and the inner surface of the upper end of the cylinder 3, and the internal space 41 of the bellows 4 and the hydrogen gas holder 1 are connected by a pipe 17. The pipe 17 is provided with a stop valve 13 . A compression spring 5 is provided between the lower surface of the piston 31 and the inner surface of the lower end of the cylinder 3.
1 is pressed upward. A manual start device 6 is attached to the valve stem 22. Inside the reaction tank 8, there is provided a container 12 composed of an air-permeable wall for holding metal hydride particles, and inside the container 12 there is provided a heat exchange fluid pipe 9 whose both ends extend outside the reaction tank. ing. Also, bellows 4 and stop valve 1
A hydrogen gas pipe 17 between pipes 1 and 3 has a stop valve 10 and a pressure reducing valve 11 in order to fill this system with hydrogen gas.
8 to which a hydrogen gas cylinder 7 is connected and, if necessary, to extract hydrogen gas from this system.
A pipe 19 with a stop valve 14 is connected.

流量調整弁2は、ベローズ内のガス圧及び弁箱23内の
ガス圧が共に一定の圧力P1以上になると、スプリング
5の押上刃、ガス圧P,による弁体21の押上刃および
ベローズ4の弾力やグランドパツセン24の摩擦力等の
機械的力などの合計された力よりもベローズ内のガス圧
がピストン31を下方に押す力の方が大きくなり、弁は
閉止状態になるように設計されている。又、流量調整弁
2の流量係数Cvは水素ガスホルダー1の圧力と、反応
槽8の圧力との差が第2図のa−b間の両曲線の差で示
されるように変動しても、質量流量が一定になるように
設計されている。以上の如く構成された蓄.放熱システ
ムのコントロール作用を以下に説明する。
In the flow regulating valve 2, when the gas pressure inside the bellows and the gas pressure inside the valve box 23 both exceed a certain pressure P1, the push-up blade of the spring 5, the push-up blade of the valve body 21 due to the gas pressure P, and the push-up blade of the bellows 4 are activated. The valve is designed so that the force of the gas pressure in the bellows pushing the piston 31 downward is greater than the total force of mechanical forces such as elasticity and frictional force of the gland fitting 24, and the valve is closed. has been done. Moreover, the flow rate coefficient Cv of the flow rate adjustment valve 2 changes even if the difference between the pressure of the hydrogen gas holder 1 and the pressure of the reaction tank 8 changes as shown by the difference between the curves a and b in FIG. , designed to have a constant mass flow rate. A storage configured as described above. The control action of the heat dissipation system will be explained below.

(放熱開始前の圧力状態は、水素ガス
ホルダー内圧力はほ\゛P,5で反応槽8の圧力P2よ
りはるかに高く、弁箱23内のガスが弁体21を押し上
げる力が小さいため、流量調整弁2は閉止状態にある。
(圧力P1は金属の種類}よび利用する熱の1温度によ
つて決定される。)放熱を開始する際、手動スタート装
置6を手動で作動させ弁2を開状態にすると、水素ガス
ホルダー1内の水素ガス管15、升2、管16を流れて
反応槽8へ流れ込む。
(The pressure state before the start of heat radiation is that the pressure inside the hydrogen gas holder is approximately P,5, which is much higher than the pressure P2 in the reaction tank 8, and the force of the gas in the valve box 23 pushing up the valve body 21 is small. The flow rate regulating valve 2 is in a closed state.
(The pressure P1 is determined by the type of metal and the temperature of the heat used.) When starting heat radiation, when the manual start device 6 is manually operated to open the valve 2, the hydrogen gas holder 1 The hydrogen gas flows through the hydrogen gas pipe 15, square 2, and pipe 16 inside, and flows into the reaction tank 8.

(な}、スタート装置は、1反応槽8の圧力またはその
中の金属水素化物や熱交換流体の温度などの信号で1駆
動させてもよい。)水素ガスが流れてホルダー1内の圧
力がP1より若干低いP1′になつた時点で、スタート
装置6を解除する。スタート装置6を解除した後、水素
ニガスホルダ一1の圧力は第2図のA,b間の実線で示
すように時間の経過と共に減少してゆき、一方反応槽8
内の圧力は鎖線で示す如く時間の経過と共に増大してゆ
く。それに伴つて流量調整弁2の開度はスプリング5、
弁体21の押上刃の合計二が漸次大きくなり、ベローズ
4内の水素ガスの押下刃は漸次・」・さくなり、ホルダ
ー1と反応槽8の圧力差が小さくなる程弁2の開度は増
大し、弁の両側の圧力差の変動にか\わらず弁の流量(
質量流量)は常に一定に保持される。したがつてその間
反応槽内8内の金属は一定質量の水素を吸蔵し、一定温
度の熱が熱交換流体管9を介して熱交換流体により回収
され、温室の暖房等に利用される。放熱過程が終了する
と、水素ガスホルダー1の圧力と反応槽8の圧力は第2
図のbの時点で示す.ように等しい温度Pmになるか、
または殆んど等しい温度になる。金属に吸蔵された水素
を元のホルダー1に戻す蓄熱過程は、風力、太陽熱、工
業廃熱から得られる熱を熱交換用流体により、熱交換用
流体管9を・介して反応槽8内の金属に与えることによ
つて行なわれる。
(The starting device may be driven by a signal such as the pressure of the reaction tank 8 or the temperature of the metal hydride or heat exchange fluid therein.) When hydrogen gas flows, the pressure inside the holder 1 increases. When the temperature reaches P1', which is slightly lower than P1, the starting device 6 is released. After releasing the starter device 6, the pressure in the hydrogen gas holder 1 decreases over time as shown by the solid line between A and b in FIG.
The internal pressure increases over time as shown by the chain line. Accordingly, the opening degree of the flow rate regulating valve 2 is adjusted by the spring 5,
The total number of push-up blades of the valve body 21 gradually increases, the push-down blade of hydrogen gas in the bellows 4 gradually becomes smaller, and the smaller the pressure difference between the holder 1 and the reaction tank 8, the more the valve 2 opens. increases, and the flow rate of the valve (
mass flow rate) is always kept constant. Therefore, during that time, the metal in the reaction tank 8 stores a certain mass of hydrogen, and heat at a certain temperature is recovered by the heat exchange fluid through the heat exchange fluid pipe 9 and used for heating the greenhouse or the like. When the heat dissipation process is completed, the pressure in the hydrogen gas holder 1 and the pressure in the reaction tank 8 are reduced to the second level.
Shown at point b in the figure. Will the temperature Pm be the same as that?
Or almost the same temperature. The heat storage process in which the hydrogen absorbed in the metal is returned to the original holder 1 is to transfer heat obtained from wind power, solar heat, and industrial waste heat into the reaction tank 8 through the heat exchange fluid pipe 9 using a heat exchange fluid. It is done by giving it to the metal.

その際、弁2は開状態にあるので、ホルダー1内の圧力
は反応槽8内の圧力と一緒に上昇する。したがつて、第
2図のb−c間では実線の曲線と鎖線の曲線とは重なる
。蓄熱過程が進むにしたがつてホルダー1及び反応槽8
の圧力は上昇し続け、その圧力がP1以上になると弁2
が閉止状態となるため、ホルダー1の圧力はそれ以上に
は上昇することはなく、蓄熱過程が終了する。
At this time, since the valve 2 is in an open state, the pressure inside the holder 1 increases together with the pressure inside the reaction tank 8. Therefore, between b and c in FIG. 2, the solid line curve and the dashed line curve overlap. As the heat storage process progresses, the holder 1 and the reaction tank 8
The pressure continues to rise, and when the pressure exceeds P1, valve 2
is in a closed state, the pressure in the holder 1 does not rise any further, and the heat storage process ends.

この時点(第2図のc)で反応槽8への熱の供給を停止
すると反応槽8内の金属が冷えて槽内の圧力は放熱過程
スタート時の圧力P2に戻る。
When the supply of heat to the reaction tank 8 is stopped at this point (c in FIG. 2), the metal inside the reaction tank 8 cools down and the pressure inside the tank returns to the pressure P2 at the start of the heat dissipation process.

またホルダー1内の圧力も水素ガスの冷えた分の圧力降
下があり、スタート時の圧力に戻る。再度、このシステ
ムから熱を回収する場合は、前述の手順を繰返せばよい
Moreover, the pressure inside the holder 1 also decreases due to the cooling of the hydrogen gas, and returns to the starting pressure. If heat is to be recovered from the system again, the above steps can be repeated.

以上の如く、本発明のコントロール方法によれば、始動
時にスタート装置を手で操作する以外は、蓄.放熱過程
の水素ガスホルダーの変化するガスの圧力を利用して、
流量調節弁の開閉及び開度の制御が行なわれるため、コ
ントローラが不要となり、これを作動させる圧力ガス源
や電源が不要となるばかりでなく、電気を使用しないた
め防爆対策が不要となり、構造が簡単になりコストダウ
ンにも効果がある。
As described above, according to the control method of the present invention, except for manually operating the starting device at the time of starting, no storage is required. Utilizing the changing gas pressure of the hydrogen gas holder during the heat dissipation process,
Since the opening/closing and opening degree of the flow control valve is controlled, a controller is not required, and a pressure gas source or power source to operate it is not required.Since no electricity is used, there is no need for explosion-proof measures, and the structure is simple. It is simple and effective in reducing costs.

上記の如く、電源等の他の施設を必要としないため、電
力の供給されていない僻地のローカルエ坏ルギ一、例え
ば野菜々園の温室の暖房等に本システムを利用する場合
、特に有利である。
As mentioned above, since no other facilities such as a power source are required, this system is particularly advantageous when used for local energy use in remote areas where there is no electricity supply, such as heating greenhouses in vegetable gardens. .

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

第1図は金属水素化物による蓄・放熱システムの水素ガ
ス流量を制御しない場合と制御した場合の放熱特性を示
す曲線図、第2図は水素ガス流量を制御した上記システ
ムに}ける放熱過程と蓄熱過程での水素ガスホルダー及
び反応槽内圧力変化曲線図、第3図は本発明の方法を実
施する蓄・放熱システムの一例の配管系統図である。 1・・・水素ガスホルダー、2・・・流量調節升、8・
・・反応槽、9・・・熱交換流体管、12・・・金属水
素化物容器。
Fig. 1 is a curve diagram showing the heat dissipation characteristics of the heat storage/dissipation system using metal hydrides when the hydrogen gas flow rate is not controlled and when the hydrogen gas flow rate is controlled, and Fig. 2 is a curve diagram showing the heat dissipation characteristics of the above system with the hydrogen gas flow rate controlled. FIG. 3 is a diagram of a pressure change curve in a hydrogen gas holder and a reaction tank during a heat storage process, and a piping system diagram of an example of a heat storage/dissipation system implementing the method of the present invention. 1...Hydrogen gas holder, 2...Flow rate adjustment box, 8.
... Reaction tank, 9... Heat exchange fluid pipe, 12... Metal hydride container.

Claims (1)

【特許請求の範囲】[Claims] 1 反応槽内に保持された金属水素化物に、水素ガスホ
ルダーより供給された水素ガスを接触させて水素を吸蔵
させその際放熱された熱を熱交換流体により回収利用し
、放熱終了後の金属水素化物に外部より熱を与えて蓄熱
させ、その際脱蔵された水素ガスを前記水素ガスホルダ
ーに回収する蓄放熱システムの自動コントロール方法に
おいて、前記ガスホルダーと反応槽とを連結する水素ガ
ス配管に流量調節弁を設け、その開閉及び流量の調節の
制御を、蓄・放熱過程における水素ガスホルダー内の水
素ガスの変動する圧力を利用して行うようにしたことを
特徴とする自動コントロール方法。
1 The metal hydride held in the reaction tank is brought into contact with hydrogen gas supplied from a hydrogen gas holder to absorb hydrogen, and the heat radiated at this time is recovered and used by a heat exchange fluid, and the metal hydride is removed after the heat radiation is completed. Hydrogen gas piping connecting the gas holder and the reaction tank in an automatic control method for a heat storage and release system in which heat is applied to a hydride from the outside to store the heat, and hydrogen gas devolatilized at the time is recovered in the hydrogen gas holder. 1. An automatic control method characterized in that a flow rate adjustment valve is provided in the holder, and the opening/closing and flow rate adjustment of the valve is controlled by utilizing the fluctuating pressure of hydrogen gas in a hydrogen gas holder during heat storage and heat release processes.
JP55150823A 1980-10-29 1980-10-29 Automatic control method of heat storage/dissipation system using metal hydrides Expired JPS591934B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55150823A JPS591934B2 (en) 1980-10-29 1980-10-29 Automatic control method of heat storage/dissipation system using metal hydrides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55150823A JPS591934B2 (en) 1980-10-29 1980-10-29 Automatic control method of heat storage/dissipation system using metal hydrides

Publications (2)

Publication Number Publication Date
JPS5774592A JPS5774592A (en) 1982-05-10
JPS591934B2 true JPS591934B2 (en) 1984-01-14

Family

ID=15505179

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55150823A Expired JPS591934B2 (en) 1980-10-29 1980-10-29 Automatic control method of heat storage/dissipation system using metal hydrides

Country Status (1)

Country Link
JP (1) JPS591934B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103913078A (en) * 2014-04-16 2014-07-09 曾建 High-temperature waste gas heat recycling device

Also Published As

Publication number Publication date
JPS5774592A (en) 1982-05-10

Similar Documents

Publication Publication Date Title
JPS6248160B2 (en)
US8323364B2 (en) Control system for an on-demand gas generator
WO2006034127A2 (en) System for maintaining hydrogen purity in electrical generators and method thereof
EP0271732B1 (en) Method of and device for storing and transforming heat and generating cold
CN114077271B (en) A high-temperature chloride salt photothermal and energy storage cycle simulation experiment platform and experiment method
CN118729840A (en) A thermochemical heat storage device and heat storage method based on metal hydride
WO2006057984A2 (en) System for monitoring the health of electrical generators and method thereof
CN118129067A (en) Energy recovery type supercritical compressed carbon dioxide energy storage system and constant pressure energy release method
JPS591934B2 (en) Automatic control method of heat storage/dissipation system using metal hydrides
US4100744A (en) Installation for the production of energy which utilizes a source of heat or natural thermic differences in level
WO2023048653A9 (en) System and method of multl-thermal energy storage for excess heat froman exothermic reactor
CN214426511U (en) Pressure stabilizing device suitable for heat storage system
JPS5738673A (en) Open/close device driven by solar heat
JPS591949B2 (en) Control method for heat exchange device with built-in hydrogen storage metal
CN108758333B (en) Carbon dioxide constant temperature and pressure regulating vaporization device
Fujitani et al. Development of hydrogen-absorbing rare earth-Ni alloys for a− 20° C refrigeration system
JPH08128596A (en) Gas evaporator and gas supply method
CN116592263B (en) An overpressure hydrogen utilization device for hydrogen storage tank
JPS5819955B2 (en) Air conditioning equipment
JPH0218281B2 (en)
US5996349A (en) Ammonia cell
JPS56144359A (en) Liquefied gas type solar heat collector
CN205374432U (en) Detect device that stores up hydrogen alloy powder and inhale hydrogen process volume change
CA2424865A1 (en) Method of absorption-desorption of hydrogen storage alloy and hydrogen storage alloy and fuel cell using said method
CN206929752U (en) A kind of shell-and-plate steam generator