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JPS597916B2 - total heat exchanger - Google Patents
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JPS597916B2 - total heat exchanger - Google Patents

total heat exchanger

Info

Publication number
JPS597916B2
JPS597916B2 JP51032213A JP3221376A JPS597916B2 JP S597916 B2 JPS597916 B2 JP S597916B2 JP 51032213 A JP51032213 A JP 51032213A JP 3221376 A JP3221376 A JP 3221376A JP S597916 B2 JPS597916 B2 JP S597916B2
Authority
JP
Japan
Prior art keywords
heat exchange
harmful gas
heat exchanger
total heat
exchange plate
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
JP51032213A
Other languages
Japanese (ja)
Other versions
JPS52115459A (en
Inventor
基之 名和
幾男 小野
正雄 牧
豊 高橋
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP51032213A priority Critical patent/JPS597916B2/en
Publication of JPS52115459A publication Critical patent/JPS52115459A/en
Publication of JPS597916B2 publication Critical patent/JPS597916B2/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
    • Y02BCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
    • Y02B30/00Energy efficient heating, ventilation or air conditioning [HVAC]
    • Y02B30/56Heat recovery units

Landscapes

  • Treating Waste Gases (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Air Filters, Heat-Exchange Apparatuses, And Housings Of Air-Conditioning Units (AREA)
  • Heat-Exchange Devices With Radiators And Conduit Assemblies (AREA)

Description

【発明の詳細な説明】 本発明は、全熱交換器においてそこを通過する空側流の
接触する熱交換面に有害ガス除去剤を配置し、人体に有
害な、NOX、SO2、H2Sなどの有害ガスの室内流
入防止を目的とするものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a total heat exchanger in which a harmful gas remover is disposed on the heat exchange surface in contact with the empty stream passing through the total heat exchanger, and removes harmful gases such as NOX, SO2, H2S, etc. that are harmful to the human body. The purpose is to prevent harmful gases from entering indoors.

本発明は有害ガスの除去と併せて、不飽和化合物等に帰
因するところの種々悪臭ガスの室内流入防止をも、目的
とするものである。
In addition to removing harmful gases, the present invention also aims to prevent various foul-smelling gases caused by unsaturated compounds from entering the room.

本発明は有害ガス除法済りを熱交換板の間隔規定部材と
して使用することを目的とするものである。
The object of the present invention is to use a material that has undergone harmful gas removal as a spacing regulating member for heat exchange plates.

従来、全熱交換器を通過する流れに対し、フィルターを
用いて空気流の清浄化を計るものがあつた。しかし、単
なるフィルターのみでは、NOx等のガス状の有害物質
の除去は不可能であつた。以下本発明の実施例につき添
付図面に泊つて詳細に説明する。第1図において、熱交
換器1は内筒2と外筒3を有し、両筒間は半径方向に区
切る熱交換板4にて、複数室に分割されている。
Conventionally, a filter has been used to purify the air flow passing through a total heat exchanger. However, it has been impossible to remove gaseous harmful substances such as NOx using a simple filter alone. Embodiments of the present invention will be described in detail below with reference to the accompanying drawings. In FIG. 1, a heat exchanger 1 has an inner cylinder 2 and an outer cylinder 3, and the space between the two cylinders is divided into a plurality of chambers by a heat exchange plate 4 that partitions the cylinder in the radial direction.

熱交換板4は紙等の適温、適温性を有するもので構成さ
れている。第1図は、複数室の一部を示したものである
。熱交換板4は、例えば、ABCD、A’B’C!D’
、A″B″C″D″にて示されるものである。ABCD
なる熱交換板4と、A’B’C’D’なる熱交換板4と
で区画された室において、CDD′C′にて形成される
閉鎖扇形部5は閉鎖状であシ、他端のABB’A’ に
て形成される開口扇形部6は、開口状態である。また開
口部7は、前記室の閉鎖扇形部5の近傍において、円周
方向に開口している。A′B′σDfなる熱交換板4と
、AIB″C″DIなる熱交換板4とで区画された室に
訃いて、A′B′BIAIにて形成される閉鎖扇形部8
は閉鎖状態であり、他端のσD′ D/′CIにて形成
される開口扇形部9は開口状態である。
The heat exchange plate 4 is made of a material having an appropriate temperature, such as paper. FIG. 1 shows a portion of a plurality of rooms. The heat exchange plate 4 is, for example, ABCD, A'B'C! D'
, A″B″C″D″. ABCD
In a chamber partitioned by heat exchange plates 4 of A'B'C'D' and heat exchange plates 4 of A'B'C'D', a closed fan-shaped portion 5 formed by CDD'C' is closed, and the other end is closed. The open fan-shaped portion 6 formed at ABB'A' is in an open state. Further, the opening 7 opens in the circumferential direction in the vicinity of the closed fan-shaped portion 5 of the chamber. A closed sector section 8 formed by A'B'BIAI is located in a chamber partitioned by a heat exchange plate 4 named A'B'σDf and a heat exchange plate 4 named AIB''C''DI.
is in a closed state, and the open fan-shaped portion 9 formed by σD'D/'CI at the other end is in an open state.

また開口部10は、前記室の閉鎖扇形部8の近傍に訃い
て、円周方向に開口している。第2図に卦いて、熱交換
器1は、壁11に設置されて訃り、開口部10は室内1
2、開口部7は室外13に位置する如〈形成している。
Further, the opening 10 is located in the vicinity of the closed fan-shaped portion 8 of the chamber and opens in the circumferential direction. In FIG. 2, the heat exchanger 1 is installed in the wall 11 and the opening 10 is in the room 1.
2. The opening 7 is formed so as to be located outside the room 13.

第3図において、14は有害ガス除法済qであり、熱交
換板4の表面に付加されている。
In FIG. 3, reference numeral 14 indicates a noxious gas removed q, which is attached to the surface of the heat exchange plate 4.

有害ガス除去剤の成分は、亜塩素酸塩(NaClO2ま
″たはKClO2)、水酸化カルシウム、硫酸カルシウ
ムである。第5図に卦いて、有害ガス除去剤14は、熱
交換板4の両面に突出し、第6図に示す如く、A,b両
方向の流れに接触する如く、配置されている。
The components of the harmful gas remover are chlorite (NaClO2 or KClO2), calcium hydroxide, and calcium sulfate.As shown in FIG. As shown in FIG. 6, it is arranged so as to be in contact with the flow in both directions A and B.

第8図に卦いて、有害ガス除去剤14は、熱交換板4間
の間隔を設定する如く、配置されている。次に作用を説
明する。第1図に卦いて、開口部7より流入する流れa
は、熱交換板ABCD,A′B′C′D′にて区画され
た室を通過し、開口扇形部6よう流出す?(フアンは図
示せず)、また開口部10より流入する流れbは、熱交
換板A5B′C′D′,AIBICIDIにて区画され
た室を通過し、開口扇形部9より流出する。
As shown in FIG. 8, the harmful gas remover 14 is arranged so as to set the interval between the heat exchange plates 4. Next, the effect will be explained. In Figure 1, the flow a flowing in from the opening 7
passes through a chamber divided by heat exchange plates ABCD, A'B'C'D' and flows out to the opening fan-shaped section 6? (The fan is not shown), and the flow b flowing in from the opening 10 passes through a chamber partitioned by the heat exchange plates A5B'C'D' and AIBICIDI, and flows out from the opening fan-shaped part 9.

(フアンは図示せず)第2図に卦いて示す如く、流れa
は室外13の空気が室内12に流入するものであり、流
れbは室内12の空気が室外13に流出するものである
(The fan is not shown) As shown in Figure 2, the flow a
Flow b is the flow of air from the outside 13 flowing into the room 12, and flow b is the flow of air from the room 12 flowing out to the outside 13.

この時、第1図において、A′BfC5D′にて示され
る熱交換板4が両流れの間に介在し、これにより高温高
湿の流れは、低温低湿の流れに、顕熱と潜熱の移動を生
じさせる。な卦夏期、室内冷房時はaからbに、冬期、
室内暖房時はbからaに熱の移動を生じる。したがつて
、室内での冷暖房機器に対する負荷を増加させることな
く、換気を行なうことが可能である。この時、熱交換板
4には、第3図に示す如く、有害ガス除去剤14が配置
されているため、第4M1fも1Δブ襦+1り ら1f
今嘘テブ1△スλT八,7′→下記に示す反応によ勺除
去される。
At this time, a heat exchange plate 4 indicated by A'BfC5D' in FIG. cause During the summer, from a to b during indoor cooling, during the winter,
During indoor heating, heat transfers from b to a. Therefore, ventilation can be performed without increasing the load on indoor heating and cooling equipment. At this time, since the harmful gas removing agent 14 is arranged on the heat exchange plate 4 as shown in FIG.
Now, it is removed by the reaction shown below.

すなわち、第2図において流れaに示される室外13か
らの空気中に、自動車の排ガス等によるNOxが、混入
していても、有害ガス除去剤の働きにより、室内12へ
送りこまれる空気は、NOxの混入していないものとな
る。
That is, even if the air from the outdoor 13 shown by flow a in FIG. 2 contains NOx due to automobile exhaust gas, etc., the air sent into the indoor 12 will be free of NOx due to the action of the harmful gas remover. It will be free of contaminants.

また、流れbに示される室内12からの空気中に、燃焼
ガス等によるNOxが混入していても、有害ガス除去剤
の働きにより、室外13へ送られる空気はNOxの混入
していないものとなる。
Furthermore, even if the air from the indoor 12 shown in flow b is mixed with NOx due to combustion gas, etc., the air sent to the outdoor 13 is assumed to be free of NOx due to the action of the harmful gas remover. Become.

第5図において、熱交換板4を通して配置された有害ガ
ス除去剤14は、空気中の水蒸気を禾用して、前記反応
を卦こさすことかられかる如く、吸湿性が強い。第6図
に訃いて、有害ガス除去剤14は、流れA,bに含まれ
ているNOxを吸収すると共に、高温高湿の流れより湿
気を吸収し、低温低湿の側に放湿することや、吸収時に
生じた凝縮潜熱を但温低湿側の幸気に与えることにより
、潜熱交換の効率をも増加しようとするものである。第
7図に}いて、熱交換板4に配置された有害ガス除去剤
14は第8図に示す如く、熱交換板4間の間隔を設定す
る如く配置されているため、流れA,bが生じても流れ
による熱交換板4相互位置の変形を生じさせないもので
ある。有害ガス除去剤の付加により、自動車の排ガス等
に含まれるNOxを除去した新鮮空気の導入が可能とな
ることや、室内での燃焼によるNOxを室外へ排出する
こともない。
In FIG. 5, the harmful gas removing agent 14 disposed through the heat exchange plate 4 has strong hygroscopicity as can be seen from the fact that it uses water vapor in the air to carry out the reaction. As shown in FIG. 6, the harmful gas remover 14 absorbs NOx contained in flows A and B, and also absorbs moisture from the high temperature and high humidity flow and releases it to the low temperature and low humidity side. The idea is to increase the efficiency of latent heat exchange by imparting the latent heat of condensation generated during absorption to the atmosphere at a lower temperature and humidity. In FIG. 7, the harmful gas remover 14 placed on the heat exchange plates 4 is arranged so as to set the interval between the heat exchange plates 4, as shown in FIG. Even if the flow occurs, the mutual position of the heat exchange plates 4 will not be deformed due to the flow. By adding a harmful gas remover, it is possible to introduce fresh air from which NOx contained in automobile exhaust gas, etc. has been removed, and NOx caused by combustion indoors is not discharged outdoors.

また、有害ガス除去剤の付加により、熱交換板表面に起
伏が生じ、通過空気流の乱れを増加するため、熱交換効
率が向土することや有害ガス除去剤の有する吸湿機能に
よV).潜熱の交換が助長され、熱交換効率が向上する
In addition, the addition of the harmful gas remover causes undulations on the surface of the heat exchange plate, which increases the turbulence of the passing airflow, resulting in a decrease in heat exchange efficiency and due to the hygroscopic function of the harmful gas remover. .. The exchange of latent heat is facilitated and the heat exchange efficiency is improved.

また、有害ガス除去剤を同時に熱交換板の間隔設定に使
用する時、熱交換板の変形がなく、熱交換の動作が確実
に行なわれるものである。
Furthermore, when the harmful gas remover is used at the same time to set the spacing between the heat exchange plates, the heat exchange plates are not deformed and the heat exchange operation is performed reliably.

以上、アルカリ金属の亜塩素酸塩、硫酸カルシウム、水
酸化カルシウムの組成物について、NOxにSO2除去
効果は式で反応は進行し、NOx除去反応よりも、反応
速度は速い。
As described above, for the composition of alkali metal chlorite, calcium sulfate, and calcium hydroxide, the reaction proceeds according to the formula for NOx and SO2 removal reaction, and the reaction rate is faster than the NOx removal reaction.

NOx除去の為の操作条件としては、環境濃度レベルの
NOxに関して空間速度SV=50,000(h−1)
程度まで10001)の除去率が得られるのに対してS
O2の場合には空間速度SV=100,000(h−1
)まで100(!l)除去率が得られる。一方、この系
はNaClO2またはKClO2を用いているので、そ
の酸化力に基づく脱臭性能がある。トリエチルアミン、
メチルメルカプタン等の悪臭物質に対しては特に有効で
ある。
The operating conditions for NOx removal are: space velocity SV = 50,000 (h-1) for NOx at the environmental concentration level;
S
In the case of O2, the space velocity SV = 100,000 (h-1
), a removal rate of 100 (!l) can be obtained. On the other hand, since this system uses NaClO2 or KClO2, it has deodorizing performance based on its oxidizing power. triethylamine,
It is particularly effective against malodorous substances such as methyl mercaptan.

NaClO2(KClO2)系が最もNOx除去能力そ
の造粒性が優れているが、他にもKMnO4Na2S2
O3,Na2SO3.CO(NH2)2系等の組成物が
有効である。
The NaClO2 (KClO2) system has the best NOx removal ability and granulation properties, but there are also KMnO4Na2S2
O3, Na2SO3. Compositions based on CO(NH2)2 and the like are effective.

それ等とNOxとの反応は、下記の通りである。これ等
1〜4の反応あるいは先のNaClO2系の反応はいづ
れも液相反応であるが、これ等の基物質にアルカリ卦よ
びセメント剤(これは水硬化性物質として定義されるが
)を加えて混練し、造粒成型した場合に、造粒品は独得
の活性反応性を示。
The reaction between them and NOx is as follows. These reactions 1 to 4 and the above NaClO2-based reaction are all liquid phase reactions, but when an alkali and a cement agent (which is defined as a hydraulic substance) are added to these base materials, When kneaded and granulated, the granulated product exhibits unique active reactivity.

その理由はNaClO2,KMnO4,・・・CO(N
H2)2などは水に対する溶解度が非常に大きい(50
〜709%/100qH20)のに対して、セメント剤
はほとんど溶解しない。そこで、造粒操作の際、水(場
合によつては、アルコールの添加が有効である)のセメ
ントに対する水和当量以上の添加状態から硬化乾燥させ
る際に水は内部から、組成物構成微粒子の間隙を毛細管
現象によつて移動し、表面に集つてそこから蒸発する際
にこれ等の易水溶性物質は、表面に集まり乾燥と共にそ
こで再結晶化する。その為に表面に多量の反応物質が集
まv、反応操作の際の表面の反応性(活性)を高めてい
ることがその理由であると考えられる。1〜4の系で3
,4系はやや反応速度が遅い。
The reason is that NaClO2, KMnO4,...CO(N
H2) 2 etc. have very high solubility in water (50
~709%/100qH20), whereas the cement agent hardly dissolves. Therefore, during the granulation operation, water (in some cases, addition of alcohol is effective) is added to the cement in an amount exceeding the hydration equivalent, and during hardening and drying, water is absorbed from the inside of the fine particles constituting the composition. As they move through the gap by capillary action, collect on the surface and evaporate from there, these easily water-soluble substances collect on the surface and recrystallize there as they dry. The reason for this is thought to be that a large amount of reactants gather on the surface, increasing the reactivity (activity) of the surface during reaction operations. 3 in the system of 1 to 4
, 4 system has a slightly slow reaction rate.

造粒性等の実用面では、NaClO2またはKClO2
系の組成物が最も性能が良く優れている。
In terms of practical aspects such as granulation properties, NaClO2 or KClO2
The system composition has the best performance and is excellent.

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

第1図は本発明の実施例に訃ける全熱交換器を示す斜視
図、第2図は全熱交換器の使用例を示す断面図、第3図
は熱交換板の平面図、第4図は熱交換板の配列状態を示
す説明図、第5図は熱交換板の第2実施例を示す平面図
、第6図は第5図の熱交換板の配列状態を示す説明図、
第7図は熱交換板の第3実施例を示す平面図、第8図は
第7図の熱交換板の配列状態を示す説明図である。 1・・・・・・熱交換器、2・・・・・・内筒、3・・
・・・・外筒、4・・・・・・熱交換板、5・・・・・
・閉鎖扇形部、6・・・・・・開口扇形部、7・・・・
・・開口部、8・・・・・・閉鎖扇形部、9・・・・・
・開口扇形部、10・・・・・・開口部、11・・・・
・・壁、12・・・・・・室内、13・・・・・・室外
、14・・・・・・有害ガス除去剤。
FIG. 1 is a perspective view showing a total heat exchanger according to an embodiment of the present invention, FIG. 2 is a sectional view showing an example of use of the total heat exchanger, FIG. 3 is a plan view of a heat exchange plate, and FIG. The figure is an explanatory diagram showing the arrangement of the heat exchange plates, FIG. 5 is a plan view showing the second embodiment of the heat exchange plate, and FIG. 6 is an explanatory diagram showing the arrangement of the heat exchange plates in FIG. 5.
FIG. 7 is a plan view showing a third embodiment of the heat exchange plate, and FIG. 8 is an explanatory diagram showing the arrangement of the heat exchange plates in FIG. 1...Heat exchanger, 2...Inner cylinder, 3...
...Outer cylinder, 4...Heat exchange plate, 5...
・Closed fan-shaped part, 6... Open fan-shaped part, 7...
・・Opening portion, 8・・Closing fan-shaped portion, 9・・・・
・Opening fan-shaped part, 10...Opening part, 11...
...Wall, 12...Indoor, 13...Outdoor, 14...Harmful gas remover.

Claims (1)

【特許請求の範囲】 1 交互に対向流を形成して対向流間の熱交換板により
全熱交換を行なわしめる機構を設け、熱交換板を紙等の
吸湿性を有する材料で、構成するとともに前記熱交換板
に有害ガス除法剤を添付した構成を有することを特徴と
する全熱交換器。 2 有害ガス除去剤がアルカリ金属の亜塩素酸塩、過マ
ンガン酸塩、亜硫酸塩、チオ硫酸塩、或いは尿素の群か
ら選んだ1種以上と、アルカリおよびセメント材に水を
加えて混練して造粒物に形成してなる有害ガス除去剤を
、熱交換板の表面に付加したことを特徴とする特許請求
の範囲第1項記載の全熱交換器。 3 有害ガス除去剤が、アルカリ金属の亜塩素酸塩、水
酸化カルシウム、硫酸カルシウムにより構成したことを
特徴とする特許請求の範囲第1項記載の全熱交換器。 4 有害ガス除去剤を熱交換板に開口した孔の中に配設
し、前記交換板両面の対向流に接触することを特徴とす
る特許請求の範囲第1項記載の全熱交換器。 5 有害ガス除去剤を熱交換板の間隔を規定する如く配
設したことを特徴とする特許請求の範囲第1項記載の全
熱交換器。
[Scope of Claims] 1. A mechanism is provided that alternately forms countercurrents and performs total heat exchange using heat exchange plates between the countercurrents, and the heat exchange plates are made of a hygroscopic material such as paper, and A total heat exchanger characterized in that the heat exchange plate has a structure in which a harmful gas removal agent is attached. 2. The harmful gas remover is made by mixing one or more selected from the group of alkali metal chlorites, permanganates, sulfites, thiosulfates, or urea with water and an alkali and cement material. 2. The total heat exchanger according to claim 1, wherein a harmful gas removing agent formed into granules is added to the surface of the heat exchange plate. 3. The total heat exchanger according to claim 1, wherein the harmful gas removing agent is composed of an alkali metal chlorite, calcium hydroxide, and calcium sulfate. 4. The total heat exchanger according to claim 1, characterized in that the harmful gas removing agent is disposed in holes opened in the heat exchange plate and comes into contact with countercurrents on both sides of the exchange plate. 5. The total heat exchanger according to claim 1, characterized in that the harmful gas removing agent is arranged to define the interval between the heat exchange plates.
JP51032213A 1976-03-23 1976-03-23 total heat exchanger Expired JPS597916B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51032213A JPS597916B2 (en) 1976-03-23 1976-03-23 total heat exchanger

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51032213A JPS597916B2 (en) 1976-03-23 1976-03-23 total heat exchanger

Publications (2)

Publication Number Publication Date
JPS52115459A JPS52115459A (en) 1977-09-28
JPS597916B2 true JPS597916B2 (en) 1984-02-21

Family

ID=12352631

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51032213A Expired JPS597916B2 (en) 1976-03-23 1976-03-23 total heat exchanger

Country Status (1)

Country Link
JP (1) JPS597916B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5926859B2 (en) * 1978-05-19 1984-07-02 松下電器産業株式会社 total heat exchanger

Also Published As

Publication number Publication date
JPS52115459A (en) 1977-09-28

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