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JPH0373798B2 - - Google Patents
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JPH0373798B2 - - Google Patents

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Publication number
JPH0373798B2
JPH0373798B2 JP11575284A JP11575284A JPH0373798B2 JP H0373798 B2 JPH0373798 B2 JP H0373798B2 JP 11575284 A JP11575284 A JP 11575284A JP 11575284 A JP11575284 A JP 11575284A JP H0373798 B2 JPH0373798 B2 JP H0373798B2
Authority
JP
Japan
Prior art keywords
heat exchange
esterified cellulose
total heat
film
cellulose
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
JP11575284A
Other languages
Japanese (ja)
Other versions
JPS60259897A (en
Inventor
Fumihide Ootsuki
Taishin Mori
Yutaka Igarashi
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.)
Toyo Netsu Kogyo Kaisha Ltd
Original Assignee
Toyo Netsu Kogyo Kaisha 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 Toyo Netsu Kogyo Kaisha Ltd filed Critical Toyo Netsu Kogyo Kaisha Ltd
Priority to JP11575284A priority Critical patent/JPS60259897A/en
Publication of JPS60259897A publication Critical patent/JPS60259897A/en
Publication of JPH0373798B2 publication Critical patent/JPH0373798B2/ja
Granted legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F28HEAT EXCHANGE IN GENERAL
    • F28FDETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
    • F28F21/00Constructions of heat-exchange apparatus characterised by the selection of particular materials

Landscapes

  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Drying Of Gases (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Laminated Bodies (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

イ 発明の目的 産業上の利用分野 本発明は全熱交換器に関するものである。 最近、住宅やビルの換気装置として熱交換器が
利用される様になり、特に顕熱交換だけではなく
潜熱交換も同時に行なうという全熱交換器が非常
に有用なものとして普及しつつある。 この全熱交換は熱交換すべき2種の気流を熱伝
導性と透湿性を有する素子で仕切つて達成される
ものである。本発明はこの全熱交換素子に関する
ものである。 従来の技術 従来の全熱交換素子としては、例えば特公昭50
−6382号の如く繊維質基材に吸湿性を有する有機
高分子樹脂を含浸付着せしめたもの、特公昭52−
10214号の如く親水性の有機高分子をフイルムを
単独で用いるもの、特公昭51−42334号の如く高
沸点多価アルコール等を含浸させた和紙又はアス
ベスト紙又は素焼きのセラミツクを用いるもの、
特開昭54−37955号の如く再生セルロースの中空
状膜に多価アルコールを含浸させたもの、特開昭
54−136570号の如く添加剤を含んだ親水性高分子
の溶液を多孔質材に含浸させてから添加材を除去
して造孔させこれに吸湿性物質を付着させたも
の、などがあげられる。 発明が解決しようとする問題点 これら従来技術において、例えば親水性高分子
を用いたものは耐水接着性が悪く素子同志を接着
させた部分が含水して剥離しやすいという大きな
欠点を有し、さらにこの親水性高分子を用いたも
のは低湿度時に透湿性が著るしく低下するという
問題点を持つている。同様に多価アルコールを用
いたものも吸湿時の接着性が弱いという短所を有
するものである。 また、これら従来技術はいずれも未だ満足すべ
き全熱交換性を有するとは云えず、この素子とし
て最も重要な物性つまりガスバリヤー性(不透気
性)と透湿性とをさらに向上させることが望まし
いと考えられる。 本発明は耐水接着性を改善しかつ透湿性とガス
バリヤー性にすぐれ、したがつて全熱交換性を向
上させることができる全熱交換素子を提供しよう
とするものである。 ロ 発明の構成 本発明の構成は、エステル化セルロースと、親
水性及び柔軟性が該エステル化セルロースよりも
大でかつそれ自身でフイルム形成能を有し該エス
テル化セルロースに対して相溶性を有する有機高
分子物質と、を含む透湿性フイルムを必須成分と
することを特徴とする全熱交換素子、を要旨とす
るものである。 問題点を解決するための手段 まずエステル化セルロースの高透湿性に着眼
し、これを単独で用いたり種々なる可塑剤を用い
て研究したが通常の可塑剤配合では透湿性が低下
し、また可塑剤が経時的に移行したり溶出したり
するので経時変化が大きいという欠点があること
を知り、さらに各種物質の配合検討を重ねたとこ
ろ、本発明と同時に提出した特許出願(特開昭60
−259896号公報参照)の如く、エステル化セルロ
ースの透湿性を維持しフイルム形成性を向上させ
しかも耐水接着性が改良されるという特定条件の
有機物質を見い出すことに成功した。それと同時
にこの特定条件の有機物質以外にも可塑剤として
作用することはないが好適なブレンド物質として
エステル化セルロースに配合でき全熱交換性を向
上させ耐水接着性を改良させることができる有機
高分子物質を選出することに成功したのである。 この有機高分子物質はエステル化セルロースと
相溶性があつて親水性及び柔軟性がエステル化セ
ルロースよりも大きくかつそれ自身でフイルム形
成能を有するというものである。 本発明においてエステル化セルロースとは、例
えば最も一般的なものとして酢酸セルロースがあ
げられ、前記の有機高分子物質としては、例えば
低酢化酢酸セルロース、低ケン化度ポリビニルア
ルコール、部分エステル化ポリアクリル酸などが
あげられる。 低酢化酢酸セルロースは基剤となる酢化度の高
い酢酸セルロースよりも親水性及び柔軟性が大き
くそれ自体でフイルム形成能を有しかつ当然に基
剤酢酸セルロースと相溶性を有するものである。 また、低ケン化度ポリビニルアルコールも上記
と同様親水性と柔軟性は酢酸セルロースよりも大
きくそれ自身でフイルム形成能があり酢酸セルロ
ースとの相溶性も有するものである。 なお、高ケン化度のポリビニルアルコールでは
酢酸セルロースとの相溶性が悪くなり、本発明の
目的には使用できないのである。 同様に部分エステル化ポリアクリル酸も上記2
種類の高分子物質と同様本発明に必要な上記物性
を備えたものである。 これら高分子物質の親水性がエステル化セルロ
ースよりも小さいと透湿性が低下し、またこれら
の高分子物質の柔軟性がエステル化セルロースよ
りも低いものではエステル化セルロースのもろさ
をカバーすることができなくなり、さらにこれら
高分子物質にフイルム形成能がない場合はエステ
ル化セルロースにブレンドするとこの配合物もフ
イルム形成能が低くなりガスバリヤー性が低下す
るのである。 なお、これら高分子物質がエステル化セルロー
スに配合されるためには相溶性が必要であること
は当然である。 また本発明におけるこれら高分子物質は上記3
種のものに限定されるものではなく、前記条件を
満足する他の如何なる有機高分子物質であつても
よいことは勿論である。 本発明素子は前記の如き有機高分子物質とエス
テル化セルロースとを適当な溶剤中で混合配合
し、これをコーテイング乾燥して透湿性フイルム
としたものである。本発明素子はこのフイルムを
単独で用いるものであつてもよいが、大抵の場合
は基材紙等の多孔性シート上にこの透湿性フイル
ムを形成させる処理をして得られたものを一体に
して使用するものである。 なお、エステル化セルロースと前記の有機高分
子物質の配合率は特に限定する必要はないが通常
前者を90〜50重量部に対して後者を10〜50重量部
配合したものが好適である。 作 用 本発明素子はエステル化セルロースが前記高分
子物質によつて柔軟化されてそのもろさがカバー
され、かつ前記高分子物質の親水性によつて透湿
性が向上し、フイルム形成性も向上するのでガス
バリヤー性にすぐれ、したがつて全熱交換性が改
良され、しかも前記高分子物質によつて耐水接着
性も良好となるのである。 実施例 1 酢化度55%で重合度150の酢酸セルロース70重
量部とブレンド高分子物質として酢化度45%で重
合度110の酢酸セルロース30重量部とをアセトン
90/メタノール10の混合溶剤に配合してブレンド
し、基材紙に固形分5g/m2となる様にコートし
風乾燥80℃にて5分間熱処理し試験片とした。 実施例 2 実施例1と同じ酢酸セルロース70重量部とブレ
ンド高分子物質としてケン化度40%のポリビニー
ルアルコール30重量部とを実施例1と同様にして
基材紙に同一付着量にコートし同様にして熱処理
し試験片とした。 比較例 1 実施例1のブレンド高分子物質の代りに酢化度
61%で重合度360の酢酸セルロースを用いて、溶
剤として塩化メチレンを使用し、他の条件は全部
実施例1と同様にして基材紙に同一付着量にコー
トし同様にして熱処理し試験片とした。 比較例 2 実施例1のブレンド高分子物質の代りに親水性
可塑剤としてポリエチレングリコールを用いて、
他の条件は実施例1と同様にして試験片を得た。 ブランクテスト 1 実施例1に用いた基材紙のみ試験片とした。 ブランクテスト 2 実施例1に用いた基材紙に実施例1の基剤酢酸
セルロースのみの溶液を固形分5g/m2の付着量
となる様にコートし同様にして熱処理して試験片
とした。 以上の各試験片についてそれぞれ蛇腹式仕切面
を介して全熱交換する全熱交換器を製作し、各々
RH62%・32℃の外気とRH40%・25℃の室内空
気との対向式全熱交換を行ない、湿度の交換効率
つまり潜熱交換効率、炭酸ガス移行率(ガス移行
性)、耐水接着性、カール現象等を測定したとこ
ろ次表の如き結果が得られた。
B. Field of Industrial Application of the Invention The present invention relates to a total heat exchanger. Recently, heat exchangers have come to be used as ventilation systems for houses and buildings, and in particular, total heat exchangers, which perform not only sensible heat exchange but also latent heat exchange at the same time, are becoming popular as extremely useful devices. This total heat exchange is achieved by partitioning the two types of air streams to be heat exchanged by an element having thermal conductivity and moisture permeability. The present invention relates to this total heat exchange element. Conventional technology As a conventional total heat exchange element, for example, the
−6382, in which a fibrous base material is impregnated with a hygroscopic organic polymer resin, Special Publication No. 52-
Those using a hydrophilic organic polymer film alone, such as No. 10214, those using Japanese paper or asbestos paper or unglazed ceramic impregnated with high boiling point polyhydric alcohol, etc., as shown in Japanese Patent Publication No. 51-42334.
A hollow membrane of regenerated cellulose impregnated with polyhydric alcohol as in JP-A No. 54-37955;
54-136570, in which a porous material is impregnated with a solution of a hydrophilic polymer containing additives, the additives are removed, pores are formed, and a hygroscopic substance is attached to the porous material. . Problems to be Solved by the Invention Among these conventional techniques, for example, those using hydrophilic polymers have a major drawback that they have poor water-resistant adhesion, and the parts where the elements are bonded contain water and are easily peeled off. Products using this hydrophilic polymer have a problem in that their moisture permeability is significantly reduced at low humidity. Similarly, those using polyhydric alcohol also have the disadvantage of weak adhesiveness when moisture is absorbed. In addition, none of these conventional technologies can be said to have satisfactory total heat exchange properties, and it is desirable to further improve the most important physical properties of this element, namely gas barrier properties (air impermeability) and moisture permeability. it is conceivable that. The present invention aims to provide a total heat exchange element that has improved water-resistant adhesion, excellent moisture permeability and gas barrier properties, and can therefore improve total heat exchange performance. B. Structure of the Invention The structure of the present invention consists of an esterified cellulose, which has greater hydrophilicity and flexibility than the esterified cellulose, has film-forming ability by itself, and is compatible with the esterified cellulose. The gist of the present invention is a total heat exchange element characterized by having, as an essential component, a moisture permeable film containing an organic polymer substance. Measures to solve the problem First, we focused on the high moisture permeability of esterified cellulose, and conducted research using it alone or with various plasticizers. After learning that the agent had the disadvantage of large changes over time as it migrated or eluted over time, and after further considering the combination of various substances, the patent application filed at the same time as the present invention (Japanese Patent Application Laid-Open No.
259896), we have succeeded in finding an organic substance that meets specific conditions, maintaining the moisture permeability of esterified cellulose, improving film forming properties, and improving water-resistant adhesion. At the same time, organic polymers that do not act as plasticizers but can be blended with esterified cellulose as a suitable blend material to improve total heat exchangeability and water-resistant adhesion can also be used in addition to organic substances under these specific conditions. They succeeded in selecting a substance. This organic polymer substance is compatible with esterified cellulose, has greater hydrophilicity and flexibility than esterified cellulose, and has film-forming ability by itself. In the present invention, esterified cellulose includes, for example, cellulose acetate as the most common one, and examples of the organic polymer substances include, for example, low acetate cellulose acetate, low saponification degree polyvinyl alcohol, partially esterified polyacrylic Examples include acids. Low-acetyl cellulose acetate is more hydrophilic and flexible than the base cellulose acetate with a high degree of acetate, has film-forming ability by itself, and is naturally compatible with the base cellulose acetate. . Similarly to the above, low saponification degree polyvinyl alcohol has greater hydrophilicity and flexibility than cellulose acetate, has film-forming ability by itself, and is compatible with cellulose acetate. Note that polyvinyl alcohol with a high degree of saponification has poor compatibility with cellulose acetate and cannot be used for the purpose of the present invention. Similarly, partially esterified polyacrylic acid is also used in the above 2.
Like other types of polymeric substances, it has the above-mentioned physical properties necessary for the present invention. If the hydrophilicity of these polymeric substances is lower than that of esterified cellulose, the moisture permeability will decrease, and if the flexibility of these polymeric substances is lower than that of esterified cellulose, it may not be possible to compensate for the brittleness of esterified cellulose. Furthermore, if these polymeric substances do not have film-forming ability, when blended with esterified cellulose, this blend also has a low film-forming ability and gas barrier properties. Note that it is a matter of course that these polymeric substances must be compatible in order to be blended into the esterified cellulose. In addition, these polymeric substances in the present invention are the above-mentioned 3
It goes without saying that the material is not limited to these types of materials, and may be any other organic polymer material that satisfies the above conditions. The device of the present invention is prepared by mixing and blending the above-mentioned organic polymeric substance and esterified cellulose in a suitable solvent, and coating and drying the mixture to form a moisture-permeable film. The device of the present invention may use this film alone, but in most cases, this film is formed by processing a porous sheet such as a base paper to form an integral film. It is used for The blending ratio of the esterified cellulose and the above-mentioned organic polymeric substance is not particularly limited, but it is usually preferable to mix 90 to 50 parts by weight of the former to 10 to 50 parts by weight of the latter. Function: In the device of the present invention, the esterified cellulose is softened by the polymer substance to cover its brittleness, and the hydrophilicity of the polymer substance improves moisture permeability and film forming properties. Therefore, it has excellent gas barrier properties, thus improving total heat exchange properties, and also has good water-resistant adhesive properties due to the polymeric substance. Example 1 70 parts by weight of cellulose acetate with a degree of acetylation of 55% and a degree of polymerization of 150 and 30 parts by weight of cellulose acetate with a degree of acetylation of 45% and a degree of polymerization of 110 as a blended polymer substance in acetone.
The mixture was blended in a mixed solvent of 90% methanol and 10% methanol, coated on a base paper to a solid content of 5 g/m 2 , air-dried and heat-treated at 80° C. for 5 minutes to prepare a test piece. Example 2 70 parts by weight of the same cellulose acetate as in Example 1 and 30 parts by weight of polyvinyl alcohol with a degree of saponification of 40% as a blended polymer substance were coated on the base paper in the same amount as in Example 1. A test piece was heat-treated in the same manner. Comparative Example 1 Acetylation degree instead of the blended polymer material of Example 1
Cellulose acetate with a polymerization degree of 61% and 360 was used, methylene chloride was used as the solvent, and all other conditions were the same as in Example 1, and the base paper was coated to the same amount and heat treated in the same manner. And so. Comparative Example 2 Using polyethylene glycol as a hydrophilic plasticizer instead of the blended polymer material of Example 1,
A test piece was obtained under the same conditions as in Example 1 except for the following conditions. Blank Test 1 Only the base paper used in Example 1 was used as a test piece. Blank test 2 The base paper used in Example 1 was coated with a solution of only the base cellulose acetate from Example 1 to a solid content of 5 g/m 2 and heat treated in the same manner to obtain a test piece. . For each of the above test specimens, we manufactured a total heat exchanger that exchanged total heat through the bellows-type partition surface, and
A two-way total heat exchange between outside air at RH 62% and 32℃ and indoor air at RH 40% and 25℃ is performed to improve humidity exchange efficiency, that is, latent heat exchange efficiency, carbon dioxide transfer rate (gas transferability), water resistance adhesion, and curl. When the phenomena were measured, the results shown in the following table were obtained.

【表】 なお、耐水接着性において○印は試験片をエチ
レン酢酸ビニル樹脂で貼合し5分間水中に浸漬し
て剥離しなかつたことを示している。またカール
現象は経時的に変化の大きいものを×印とし、や
や変化するものを△印とし変化のほとんどないも
のを○印とした。 この表より、実施例1および2は潜熱交換性つ
まり透湿性にすぐれ、しかもガスバリヤー性も良
好でかつ耐水接着性も高いことが認められ、比較
例1は基剤酢酸セルロースのもろさをカバーでき
ないのでブランクテスト2と同様カール現象が著
るしいという欠点を有するものとなつている。ま
た、比較例2はガスバリヤー性及び耐水接着性が
悪く、ブランクテスト1はガスバリヤー性が非常
に低いものとなつている。 さらに実施例1及び2は酢酸セルロースの欠点
であるもろさをカバーしフイルム形成性を向上さ
せているのである。 ハ 発明の効果 以上詳細に説明した様に本発明における全熱交
換素子は、エステル化セルロースに柔軟性と親水
性の高い高分子物質をブレンドすることによつて
エステル化セルロースの透湿性を向上させると共
にそのもろさをカバーし、かつフイルム形成性を
改良してそのガスバリヤー性を向上させ、したが
つて全熱交換素子として非常に有用であり、しか
も耐水接着性にすぐれているので素子間の接着部
が吸湿時に剥れることもないというすぐれた効果
を奏するものである。
[Table] Note that in terms of water-resistant adhesion, the mark ○ indicates that the test piece was laminated with ethylene vinyl acetate resin and did not peel off after being immersed in water for 5 minutes. In addition, regarding the curl phenomenon, those with large changes over time are marked with an "x", those with a slight change are marked with a △, and those with almost no change are marked with an ○. From this table, it can be seen that Examples 1 and 2 have excellent latent heat exchange properties, that is, moisture permeability, and also have good gas barrier properties and high water-resistant adhesion, while Comparative Example 1 cannot overcome the brittleness of the base cellulose acetate. Therefore, like Blank Test 2, this test has the disadvantage that the curling phenomenon is significant. Furthermore, Comparative Example 2 had poor gas barrier properties and water-resistant adhesive properties, and Blank Test 1 had very low gas barrier properties. Furthermore, Examples 1 and 2 overcome the fragility, which is a drawback of cellulose acetate, and improve film-forming properties. C. Effects of the Invention As explained in detail above, the total heat exchange element of the present invention improves the moisture permeability of esterified cellulose by blending the esterified cellulose with a polymeric substance having high flexibility and hydrophilicity. At the same time, it overcomes its brittleness, improves its film formation properties, and improves its gas barrier properties, making it extremely useful as a total heat exchange element.Moreover, it has excellent water-resistant adhesion properties, making it suitable for adhesion between elements. This has the excellent effect of preventing the parts from peeling off when they absorb moisture.

Claims (1)

【特許請求の範囲】 1 エステル化セルロースと、親水性及び柔軟性
が該エステル化セルロースよりも大でかつそれ自
身でフイルム形成能を有し該エステル化セルロー
スに対して相溶性を有する有機高分子物質と、を
含む透湿性フイルムを必須成分とすることを特徴
とする全熱交換素子。 2 多孔性シート上に必須成分である透湿性フイ
ルムが処理されている特許請求の範囲第1項記載
の全熱交換素子。
[Scope of Claims] 1. Esterified cellulose, and an organic polymer that has greater hydrophilicity and flexibility than the esterified cellulose, has film-forming ability by itself, and is compatible with the esterified cellulose. A total heat exchange element characterized in that an essential component is a moisture permeable film containing a substance. 2. The total heat exchange element according to claim 1, wherein a moisture permeable film, which is an essential component, is treated on the porous sheet.
JP11575284A 1984-06-05 1984-06-05 Total heat exchange element Granted JPS60259897A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11575284A JPS60259897A (en) 1984-06-05 1984-06-05 Total heat exchange element

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11575284A JPS60259897A (en) 1984-06-05 1984-06-05 Total heat exchange element

Publications (2)

Publication Number Publication Date
JPS60259897A JPS60259897A (en) 1985-12-21
JPH0373798B2 true JPH0373798B2 (en) 1991-11-22

Family

ID=14670169

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11575284A Granted JPS60259897A (en) 1984-06-05 1984-06-05 Total heat exchange element

Country Status (1)

Country Link
JP (1) JPS60259897A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010167339A (en) * 2009-01-21 2010-08-05 Seiichi Manabe Apparatus and method of removing moisture in gas
JP7089178B2 (en) * 2018-07-23 2022-06-22 ダイキン工業株式会社 Total heat exchange element and its manufacturing method
CN116940797A (en) * 2021-03-02 2023-10-24 三菱制纸株式会社 Moisture permeable film for total heat exchange element and total heat exchange element

Also Published As

Publication number Publication date
JPS60259897A (en) 1985-12-21

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