JPS6328428A - Drying agent - Google Patents

Drying agent

Info

Publication number
JPS6328428A
JPS6328428A JP17133686A JP17133686A JPS6328428A JP S6328428 A JPS6328428 A JP S6328428A JP 17133686 A JP17133686 A JP 17133686A JP 17133686 A JP17133686 A JP 17133686A JP S6328428 A JPS6328428 A JP S6328428A
Authority
JP
Japan
Prior art keywords
polytetrafluoroethylene
moisture
fine particles
moisture absorbent
hygroscopic
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
JP17133686A
Other languages
Japanese (ja)
Other versions
JPH0749091B2 (en
Inventor
Choichi Furuya
長一 古屋
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.)
SHIRAKAWA SEISAKUSHO KK
Original Assignee
SHIRAKAWA SEISAKUSHO KK
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 SHIRAKAWA SEISAKUSHO KK filed Critical SHIRAKAWA SEISAKUSHO KK
Priority to JP61171336A priority Critical patent/JPH0749091B2/en
Publication of JPS6328428A publication Critical patent/JPS6328428A/en
Publication of JPH0749091B2 publication Critical patent/JPH0749091B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Drying Of Gases (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

PURPOSE:To obtain a drying agent which is easy in handling and free in molding and deformation and high in strength and difficult-to cause a crack at a time for heating and regenerating it and is free from environmental pollution by a liquefied moisture absorbent by sticking moisture absorbent fine particles by polytetrafluoroethylene. CONSTITUTION:A drying agent is obtained by kneading moisture absorbent fine particles such as synthesized zeolite, polytetrafluoroethylene and solvent naphtha, etc., and molding this mixture into a sheet-shape or the like by pressurizing rolls and drying this molded article. Furthermore a moisture absorbent 3 such as lithium chloride is deposited on the moisture absorbent fine particles 1 by absorbing an alcoholic soln. of lithium chloride thereto and drying it and thereby the drying agent bonded by polytetrafluoroethylene 2 is obtained.

Description

【発明の詳細な説明】 「産業上の利用分野」 この発明は、ペレット状ないし、粉末のみならず、種々
の形状に成形することができ、しかも水分を吸収して液
化した吸湿剤が使用中に漏出することを防止するととも
に、吸湿剤の水分吸収能力を最大限に利用できるように
して、多量の水分を吸収保持できるようにした乾燥材に
関するものである。
Detailed Description of the Invention "Industrial Application Field" This invention is a moisture absorbent that can be molded into various shapes, including pellets and powder, and which absorbs moisture and liquefies it. The present invention relates to a desiccant material that absorbs and retains a large amount of moisture by preventing moisture from leaking into water and making maximum use of the moisture absorption ability of the moisture absorbent.

「従来の技術」 従来の乾燥材は、第5図に示すように吸湿性のある微粒
子をそのままか、またはペレット状の一定の形状に成型
して、本法気の透過性を有する除湿ロータ11等の容器
に入れて使用している。そして、この吸湿性のある粒子
に湿気を含んだ空気を供給して除湿し、またその一部に
加熱した再生空気を供給して吸湿性のある粒子を再生し
ながら使用するものが多い。
``Prior Art'' As shown in FIG. 5, conventional desiccant materials are made by using hygroscopic fine particles as they are or by molding them into a pellet-like shape to form a dehumidifying rotor 11 that is permeable to air. I use it in a container such as In many cases, the hygroscopic particles are supplied with humid air to dehumidify them, and some of the hygroscopic particles are supplied with heated regeneration air to regenerate the hygroscopic particles.

また、アスベスト布ないしその他の担持材に塩化リチウ
ム、塩化カルシウム等の吸ls剤を保持させた乾燥材も
知られている。
Also known is a drying material in which an asbestos cloth or other supporting material holds an absorbent such as lithium chloride or calcium chloride.

「発明が解決しようとする問題へ」 しかしながら、上記吸湿性のある粒子はペレット状ない
し粉末で使用されることが多く、その取扱いがjト常に
面倒で、使用中にこすり合わされて蛍粉化し、これが飛
散して環境を汚染してしまうという欠点があった。
``Towards the problem to be solved by the invention'' However, the above-mentioned hygroscopic particles are often used in the form of pellets or powder, which are always difficult to handle, and are rubbed together during use and turn into fluorescein. This has the disadvantage that it scatters and pollutes the environment.

また上記吸湿剤は、その吸湿能力が大きければ犬、きい
程、水分を吸収すると吸湿剤自身が液化するものが多く
(例えば、112化リチウム、臭化リチウム・、塩化カ
ルシウム等)、これらの液化した吸湿剤は、たとえ除湿
ロータ11等の容器に封入されていても、その系から漏
出し、他の機器や材料に付nすること等によって項境を
汚染しがちであるという欠点があった。
In addition, the higher the moisture absorption capacity of the moisture absorbent, the higher the moisture absorbency, and many of the moisture absorbents themselves liquefy when they absorb moisture (for example, lithium 112 chloride, lithium bromide, calcium chloride, etc.). Even if the hygroscopic agent is sealed in a container such as the dehumidifying rotor 11, it has the disadvantage that it tends to leak out of the system and contaminate the environment by being attached to other equipment or materials. .

この発Illは、これらの欠点を解消した乾燥材を提供
しようとするものである。
This invention aims to provide a desiccant material that eliminates these drawbacks.

「問題を解決するための手段」 すなわちこの発明の乾燥材は、従来例の上記欠(”尺を
解消するため、その実施例を説明する第1図に示された
ように、先ず第1に、水分を吸着して保持する性質を有
する吸湿性微粒子lを、ポリテトラフルオロエチレン2
で結着し、吸湿性微粒子1の周囲にポリテトラフルオロ
エチレン2の、1fM l−1伏字間4を形成し、この
、網目状空間4を木へ気の透過通路としたものである。
``Means for solving the problem'' In other words, in order to solve the above-mentioned deficiencies in the conventional example, the drying material of the present invention first solves the problems as shown in FIG. , hygroscopic fine particles l having the property of adsorbing and retaining moisture are added to polytetrafluoroethylene 2
The hygroscopic fine particles 1 are bound together to form a 1 fM l-1 hollow space 4 of polytetrafluoroethylene 2 around the hygroscopic fine particles 1, and this mesh space 4 is used as a passage for air to pass through to the wood.

そのため、内部の吸湿性微粒子に水へ気が容易に供給さ
れ、吸湿速度が大きい。
Therefore, water is easily supplied to the internal hygroscopic particles, resulting in a high moisture absorption rate.

また第2に、この発明の乾燥材は、水分を吸収して液化
する性質を有する吸湿剤3を吸湿性微粒子−1等の周囲
に拘持させ、これをポリテトラフルオロエチレン2で結
着し、吸湿剤3の周囲にポリテトラフルオロエチレン2
の、網目状空間4を形成し、この、網目状空間4を水)
N気の透過通路として吸湿剤3に水分を吸収させ、さら
に、網目状空間4の側壁をポリテトラフルオロエチレン
2の疎水性を有する面とし、水分をその表面I張力で保
持させて、水分を吸収した吸湿剤3の漏出防止と、吸湿
剤3の水分吸収能力を最大限に利用できるようにしたも
のである。すなわち、吸湿剤に水分が吸収されて吸湿剤
が液状になっても、1網「1伏字間4は撥水性のポリテ
トラフルオロエチレン2の、網目状−F間であるため、
外部に浸み出ることはない。
Secondly, the desiccant material of the present invention has a hygroscopic agent 3 having a property of absorbing moisture and liquefying it, which is held around the hygroscopic fine particles 1, etc., and bound with polytetrafluoroethylene 2. , polytetrafluoroethylene 2 is placed around the moisture absorbent 3.
form a mesh-like space 4, and fill this mesh-like space 4 with water)
Moisture is absorbed by the moisture absorbent 3 as a permeation path for N gas, and the side wall of the mesh space 4 is made into a hydrophobic surface of the polytetrafluoroethylene 2, and the moisture is retained by the surface I tension. This prevents the absorbed moisture absorbent 3 from leaking and makes maximum use of the moisture absorbing ability of the moisture absorbent 3. In other words, even if moisture is absorbed by the moisture absorbent and the moisture absorbent becomes liquid, the 1 mesh 4 is between the mesh and F of the water-repellent polytetrafluoroethylene 2.
It does not leak to the outside.

この場合の乾燥材は、実際にはシリカゲル等の吸湿性全
粒子lをポリテトラフルオロエチレン2で結着し、ある
いは塩化リチウム等の吸湿剤3をシリカゲル等の吸湿性
微粒子lに浸み込ませて。
In this case, the drying material is actually made by binding all hygroscopic particles such as silica gel with polytetrafluoroethylene 2, or by impregnating hygroscopic particles such as silica gel with a hygroscopic agent 3 such as lithium chloride. hand.

これをポリテトラフルオロエチレン2で結着し、ベレ7
)またはシート状に成形あるいは加工したものを用いる
。吸湿性微粒子1をポリテトラフルオロエチレン2で結
着すると、ポリテトラフルオロエチレン2の全粒子の周
囲に水分を保持する網目状空間4が多量に形成されるの
で、吸湿性微粒(−1や吸湿剤3の効果を最大限に発揮
させることができる。
This is bound with polytetrafluoroethylene 2, and the beret 7
) or molded or processed into a sheet. When hygroscopic fine particles 1 are bound with polytetrafluoroethylene 2, a large amount of mesh spaces 4 that retain moisture are formed around all the particles of polytetrafluoroethylene 2, so that hygroscopic fine particles (-1 and hygroscopic The effect of Agent 3 can be maximized.

第3に、第2図に示すように、吸湿性微粒子1を撥水性
を有するポリテトラフルオロエチレンの微孔性被膜5で
被覆すれば、液化した吸湿剤(水分)を保持している。
Thirdly, as shown in FIG. 2, if the hygroscopic fine particles 1 are coated with a microporous coating 5 made of water-repellent polytetrafluoroethylene, the liquefied hygroscopic agent (moisture) is retained.

網u伏字間4から、吸湿剤が漏出することもなく、多量
の水分を吸着して保持することができる。
A large amount of moisture can be adsorbed and retained without the moisture absorbent leaking out from the dotted lines 4.

しまたがってこの場合の乾燥材は、第1の場合の乾燥材
を内在するとともに、前記被膜がポリテトラフルオロエ
チレン多孔質膜または撥水性微粒子とポリテトラフルオ
ロエチレンの複合多孔質被膜である。すると水分を含む
気体は2疎木性を有するポリテトラフルオロエチレン多
孔質被膜をA&し、内部の吸湿性微粒子や吸湿剤に水分
を吸収ないし吸着され、やがては膨潤ないし液化するが
、その吸湿性微粒子ないし吸湿剤に保持ごれた水分は外
面の疎水性のポリテトラフルオロエチレンの被膜に遮断
されて外部に漏出することがない0表面がポリテトラフ
ルオロエチレンであるため、吸湿剤の微粉化等もなく、
クリーンな乾燥気体が得られる。
Moreover, the desiccant material in this case contains the desiccant material in the first case, and the coating is a polytetrafluoroethylene porous membrane or a composite porous coating of water-repellent fine particles and polytetrafluoroethylene. Then, the moisture-containing gas passes through the polytetrafluoroethylene porous coating, which has 2 lignophobic properties, and the moisture is absorbed or adsorbed by the hygroscopic fine particles and hygroscopic agent inside, and eventually swells or liquefies, but its hygroscopicity The moisture retained in the fine particles or moisture absorbent is blocked by the hydrophobic polytetrafluoroethylene coating on the outer surface and does not leak to the outside.Since the surface is polytetrafluoroethylene, the moisture absorbent can be pulverized, etc. Without any
Clean dry gas is obtained.

なお、前記被膜は、成形された乾燥材を補強する効果も
ある。
Note that the coating also has the effect of reinforcing the molded desiccant material.

さらにこの発明の乾燥材は、第3図に示す例のようにシ
ート状に成形された原反6に凹凸加工を施し、これを丸
めて使用することができる。したがって、その長さ方向
に水へ気を通すことかでさる。また、第4図に示す例の
ようにハニカム状に加工して所定の径の貫通孔8を右す
るハニカム構造物7とし、この貫通孔8に水蒸気を通す
ことによって使用することができる。
Furthermore, the desiccant material of the present invention can be used by applying unevenness to a sheet-shaped original fabric 6, as shown in the example shown in FIG. 3, and rolling it up. Therefore, it is important to allow air to pass through the water along its length. Further, as shown in the example shown in FIG. 4, the honeycomb structure 7 can be processed into a honeycomb shape and has through holes 8 of a predetermined diameter on the right side, and can be used by passing water vapor through the through holes 8.

「発明の効果」 この発明の乾燥材は以上のように構成されているので、
従来のベレット状ないし粉末のものと異なってその取扱
いが容易であり、しかも従来のベレット状ないし粉末の
ものはそれ以外の態様を取得ないが、この発明の乾燥剤
は自由に成形ないし変形でき、種々の態様を採り得るの
で広範な用途に使用することができる。
"Effects of the Invention" Since the drying material of this invention is configured as described above,
Unlike the conventional pellet-like or powder-like desiccant, it is easy to handle, and while the conventional pellet-like or powder-like desiccant does not have any other features, the desiccant of the present invention can be freely molded or deformed, Since it can take various forms, it can be used for a wide range of purposes.

また、非常に強度があり、加熱再生して使用する場合に
もクラックが入りにくく、長期間に亘って使用すること
ができる。
In addition, it is extremely strong and does not easily crack when used after being heated and regenerated, so it can be used for a long period of time.

さらに、液化した吸湿剤(水分)を保持している。tl
11目状空間から吸湿剤が漏出することもなく。
Furthermore, it retains liquefied moisture absorbent (moisture). tl
No moisture absorbent leaks from the 11-eye space.

外部環境を汚すことなく、多量の水分を吸着して保持す
ることができる。
It can adsorb and retain large amounts of moisture without polluting the external environment.

この発明の乾燥剤は、従来と同様の乾燥機用の乾燥材と
して、あるいは壁材等として使用することができる。ま
た特に、吸湿剤を含むものは水分を多植に吸収もしくは
放出できるので、湿度コントロール用の材料としても使
用できる。
The desiccant of the present invention can be used as a desiccant for conventional dryers, or as a wall material. Moreover, in particular, those containing a moisture absorbent can absorb or release moisture, so they can also be used as materials for humidity control.

以下、この発明の乾燥材を実施例にしたがって詳細に説
明する。
Hereinafter, the desiccant material of the present invention will be explained in detail according to Examples.

「実施例」 実施例1 合成ゼオライト(Silton  B  商品名木沢化
学株式会社製): PTFE (D−1商品名 ダイキ
ン工業株式会社製):ソルベントナフサを9:1:20
の割合で混練し、加圧ロールで所定の厚さのシート状に
成形した。このシート状物を280℃で3時間加熱し、
厚さ1.5mmのシートを得た。このシートを125c
m2に切り取り、150℃で乾燥すると14.OOgと
なりこれを試料1とした。この試料1を21℃、30%
RHで6時間放置したところ、水分を吸収して15.7
5gとなった。したがって1.75gの水分を吸収した
ことがわかる。
"Example" Example 1 Synthetic zeolite (Silton B, product name, manufactured by Kizawa Chemical Co., Ltd.): PTFE (D-1 product name, manufactured by Daikin Industries, Ltd.): Solvent naphtha in a ratio of 9:1:20
The mixture was kneaded in the following proportions and formed into a sheet with a predetermined thickness using a pressure roll. This sheet-like material was heated at 280°C for 3 hours,
A sheet with a thickness of 1.5 mm was obtained. This sheet is 125c
Cut into m2 pieces and dry at 150°C. 14. OOg, and this was designated as sample 1. This sample 1 was heated to 21℃ and 30%
When left at RH for 6 hours, it absorbed moisture and became 15.7
It became 5g. Therefore, it can be seen that 1.75 g of water was absorbed.

また上記試料1にLiClをアルコール溶液として4.
5g吸収させ、150℃で乾燥すると18.56gとな
り、これを試料2とした。この試料2を21℃、30%
RHで6時間数lしたところ、水分を吸収して27.4
0gとなり、8.84gの水分を吸収した。しかもシー
トの表面に口紙をつけても、水分その他の移動はなかっ
た。
In addition, 4. LiCl was added to the sample 1 as an alcohol solution.
When 5g was absorbed and dried at 150°C, the amount was 18.56g, which was designated as sample 2. This sample 2 was heated to 21℃ and 30%
When exposed to several liters at RH for 6 hours, it absorbed moisture and became 27.4
0g, and absorbed 8.84g of water. Furthermore, even when a paper was attached to the surface of the sheet, there was no movement of moisture or other substances.

実施例2 合成ゼオライト(SilLon  B  商品名水沢化
学株式会社製): PTFE (D−1商品名 ダイキ
ン工業株式会社製):ソルベントナフサを7=3・20
の割合で混練し 加圧ロールで所定の厚さのシート状に
成形した。このシート状物を280℃で3時間加熱し、
ソルベントナフサと界面活性剤を除いて厚さ0.75m
mのシートを(1)だ。このシートを125cm2に切
り取り、130℃で乾燥するとio、12gとなった。
Example 2 Synthetic zeolite (SilLon B trade name, manufactured by Mizusawa Chemical Co., Ltd.): PTFE (D-1 trade name, manufactured by Daikin Industries, Ltd.): Solvent naphtha at 7 = 3.20
The mixture was kneaded at a ratio of 1, and then formed into a sheet with a predetermined thickness using a pressure roll. This sheet-like material was heated at 280°C for 3 hours,
Thickness 0.75m excluding solvent naphtha and surfactant
The sheet of m is (1). This sheet was cut into 125 cm 2 and dried at 130° C. to give a weight of 12 g.

これに吸湿剤として、1.7gのLiCIをアルコール
溶液として浸み込ませた。これを130℃で乾燥すると
、l l 、82gの試#1が得られた。この試料を2
2℃、30%RHで2詩間jI!!置したところ、水分
を3.35g吸収して15.15gとなった。このとき
結露現象は、PTFEの網目のために起きない。
This was impregnated with 1.7 g of LiCI as a moisture absorbent in the form of an alcohol solution. When this was dried at 130° C., 82 g of sample #1 was obtained. This sample
2 poems at 2℃ and 30%RH! ! When it was left to stand, it absorbed 3.35g of water and became 15.15g. At this time, dew condensation does not occur due to the PTFE mesh.

実施例3 合成ゼオライト(ゼオスターNP  IQOP  商品
名 日本化学工業株式会社製): PTFE (D−1
商品名 ダイキン工業株式会社!A):ソルベントナフ
サを9:1:20の割合で混練し、加圧ロールで所定の
厚さのシート状に成形した。このシート状物を280℃
で3時間加熱し、厚さ1゜4mmのシートを得た。この
シートを100cm2に切り取り、150℃で乾燥する
と14.28gとなった。この試料を25℃、43%R
Hの室ニ3時間放置したところ、16.76gとなり、
水分を2.48g吸収した。
Example 3 Synthetic zeolite (Zeostar NP IQOP, trade name, manufactured by Nihon Kagaku Kogyo Co., Ltd.): PTFE (D-1
Product name Daikin Industries, Ltd.! A): Solvent naphtha was kneaded in a ratio of 9:1:20 and formed into a sheet of a predetermined thickness using a pressure roll. This sheet-like material was heated to 280°C.
The mixture was heated for 3 hours to obtain a sheet with a thickness of 1.4 mm. This sheet was cut into 100 cm 2 pieces and dried at 150° C. to give a weight of 14.28 g. This sample was heated at 25℃ and 43%R.
When I left it in room H for 3 hours, it weighed 16.76g.
Absorbed 2.48g of water.

実施例4 合成ゼオライト(ゼオスターNP  LOOP  商品
名 日木化学工業株式会社:V): PTFE (D−
1商品名 ダイキン工業株式会社製):ソルベントナフ
サを9.5:0.5:20の割合で混練し1加圧ロール
で所定の厚さのシート状に成形した。このシート状物を
280℃で3時間加熱し、11さ1.3mmのシートを
得た。このシートを100cm2に切り取り、150℃
で乾燥すると12.04gとなった。この試料を25℃
、40%RHの室に2時間数にしたところ、14.35
gとなり、水分を2.31g吸収した。
Example 4 Synthetic zeolite (Zeostar NP LOOP, trade name: Hiki Chemical Industry Co., Ltd.: V): PTFE (D-
1 (trade name, manufactured by Daikin Industries, Ltd.): Solvent naphtha was kneaded in a ratio of 9.5:0.5:20 and formed into a sheet of a predetermined thickness using one pressure roll. This sheet-like material was heated at 280° C. for 3 hours to obtain a sheet with a diameter of 11.3 mm. Cut this sheet into 100cm2 pieces and heat at 150°C.
When dried, the weight was 12.04 g. This sample was heated at 25°C.
, when placed in a room with 40% RH for 2 hours, the result was 14.35
g, and absorbed 2.31 g of water.

実施例5 シリカゲル(ミズカジルP73  商品名 水沢化学株
式会社製): PTFE (D−1商品名ダイキン工業
株式会社製):ソルベントナフサを7・3:20の割合
で混練し、加圧ロールで所定の厚ざのシート状に成形し
た。このシート状物を280℃で3時間加熱し、厚さ2
.0mmのシートを得た。このシートを125cm2!
l/]り取り、LiC1のアルコール溶液を4.5g浸
み込ませた。これを100℃で乾燥すると21.56g
となった。この試料を22℃、32%RHの室に3時間
放置したところ、9.00gの水分を吸収して30.5
6gとなった。そしてこの試料には、表面に水滴が生じ
ることはなかった。
Example 5 Silica gel (Mizukasil P73, trade name, manufactured by Mizusawa Chemical Co., Ltd.): PTFE (D-1, trade name, manufactured by Daikin Industries, Ltd.): Solvent naphtha were kneaded in a ratio of 7.3:20, and the mixture was mixed with a pressure roll to a predetermined level. It was formed into a thick sheet. This sheet-like material was heated at 280°C for 3 hours, and the thickness was 2
.. A sheet of 0 mm was obtained. This sheet is 125cm2!
1/] and soaked with 4.5 g of an alcohol solution of LiC1. When this is dried at 100℃, it weighs 21.56g.
It became. When this sample was left in a room at 22°C and 32% RH for 3 hours, it absorbed 9.00g of water and 30.5g of water was absorbed.
It became 6g. No water droplets were observed on the surface of this sample.

実施例6 合成ゼオライ) (TSZ640  商品名 東洋ソー
ダ株式会社製):PTFEファインパウダー(ポリフロ
ンファインパウダー 商品名 ダイキン工業株式会社製
)を6.5:3.5の割合でミキサーで混合し、この粉
末を380℃、200kg/cm2でプレスし、130
cm2.厚さ2゜0mmの板を得た。この板に吸湿剤と
してLiC1のアルコール溶液を3.Og浸み込ませた
。これを100℃で乾燥すると、34.69gとなった
。この試料を21℃、30%RHの室に5時間放置した
ところ、水分を吸収して40.72gとなり、6.03
gの水分を吸収した。この試料は強固で、プレス成形に
よりハニカム状等、必要に応じて最適な除湿板構造のも
のが得られた。
Example 6 Synthetic zeolite) (TSZ640, trade name, manufactured by Toyo Soda Co., Ltd.): PTFE fine powder (Polyflon Fine Powder, trade name, manufactured by Daikin Industries, Ltd.) were mixed in a mixer at a ratio of 6.5:3.5, and this The powder was pressed at 380℃ and 200kg/cm2, and
cm2. A plate with a thickness of 2°0 mm was obtained. An alcoholic solution of LiC1 was applied to this plate as a moisture absorbent. It was soaked with Og. When this was dried at 100° C., the weight was 34.69 g. When this sample was left in a room at 21°C and 30% RH for 5 hours, it absorbed water and weighed 40.72g, which was 6.03g.
Absorbed g of water. This sample was strong, and by press molding, a honeycomb-like or other suitable dehumidifying plate structure was obtained as required.

実施例7 アセチレンブラツク: PTFE (D−1商品名 ダ
イキン工業株式会社!W):ソルベントナフサを6:4
:20の割合で混、錬し、加圧ロールで所定の厚さのシ
ート状に成形した。このシート状物を280℃で3時間
加熱し、厚さ0.85mmのシートを得た。このシート
を160cm2切り取り、吸湿剤としてLiC1のメタ
ノール溶液を1.0g浸み込ませた。これを100℃で
20分加熱乾燥したところ5.20gであった。この試
料を22℃、32%RHの室に4時間数こしたところ、
8.08[となり、水分を1.92g吸収した。
Example 7 Acetylene black: PTFE (D-1 product name Daikin Industries, Ltd.!W): Solvent naphtha 6:4
:20 and then formed into a sheet of a predetermined thickness using a pressure roll. This sheet-like material was heated at 280° C. for 3 hours to obtain a sheet with a thickness of 0.85 mm. A 160 cm 2 piece of this sheet was cut out, and 1.0 g of a methanol solution of LiC1 was impregnated therein as a moisture absorbent. When this was heated and dried at 100° C. for 20 minutes, the weight was 5.20 g. When this sample was strained in a room at 22°C and 32% RH for several hours,
8.08[, and absorbed 1.92g of water.

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

第1図はこの発明の乾燥材の一実施例を示す概略断面図
、第2図は他の実施例を示す断面図、第3図および第4
図はこの発明の乾燥材を用いて形成した成形品の斜視図
、第5図は貨来の乾燥材の使用状態を示す概略図である
。 1・・・吸湿性a粒子 2・・・ポリテトラフルオロエチレン 3・・・吸湿剤       4・・・、IM [1伏
字間5・・・撥水性被膜 第 5 目 第1図 第2図 第3図 第 4 区
FIG. 1 is a schematic sectional view showing one embodiment of the desiccant material of the present invention, FIG. 2 is a sectional view showing another embodiment, and FIGS.
The figure is a perspective view of a molded article formed using the desiccant material of the present invention, and FIG. 5 is a schematic diagram showing the state in which the conventional desiccant material is used. 1... Hygroscopic a particles 2... Polytetrafluoroethylene 3... Hygroscopic agent 4..., IM [1 between blanks 5... Water repellent coating No. 5 Eye 1 Figure 2 Figure 3 Figure 4th ward

Claims (1)

【特許請求の範囲】 1、吸湿性微粒子をポリテトラフルオロエチレンで結着
したことを特徴とする乾燥材。 2、吸湿性微粒子が、吸湿剤を担持部材に担持させて形
成してなる特許請求の範囲第1項記載の乾燥材。 3、吸湿性微粒子が、親水性微粒子をポリテトラフルオ
ロエチレンで結着させてなり、これに吸湿剤を担持させ
てなる特許請求の範囲第2項記載の乾燥材。 4、吸湿性微粒子が、ポリテトラフルオロエチレンの多
孔質被膜または撥水性を有するポリテトラフルオロエチ
レン複合多孔質被膜で被覆されたことを特徴とする特許
請求の範囲第1項ないし第3項のいずれかに記載の乾燥
材。
[Scope of Claims] 1. A drying material characterized in that hygroscopic fine particles are bound with polytetrafluoroethylene. 2. The drying material according to claim 1, wherein the hygroscopic fine particles are formed by supporting a hygroscopic agent on a supporting member. 3. The desiccant material according to claim 2, wherein the hygroscopic fine particles are formed by binding hydrophilic fine particles with polytetrafluoroethylene and carrying a hygroscopic agent thereon. 4. Any one of claims 1 to 3, characterized in that the hygroscopic fine particles are coated with a polytetrafluoroethylene porous coating or a water-repellent polytetrafluoroethylene composite porous coating. Dried material listed in Crab.
JP61171336A 1986-07-21 1986-07-21 Dry material and method of manufacturing dry material Expired - Lifetime JPH0749091B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61171336A JPH0749091B2 (en) 1986-07-21 1986-07-21 Dry material and method of manufacturing dry material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61171336A JPH0749091B2 (en) 1986-07-21 1986-07-21 Dry material and method of manufacturing dry material

Publications (2)

Publication Number Publication Date
JPS6328428A true JPS6328428A (en) 1988-02-06
JPH0749091B2 JPH0749091B2 (en) 1995-05-31

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ID=15921336

Family Applications (1)

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

Country Link
JP (1) JPH0749091B2 (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63264125A (en) * 1987-04-18 1988-11-01 Kobe Steel Ltd Dry dehumidifying component
JP2002280166A (en) * 2001-01-12 2002-09-27 Japan Gore Tex Inc Organic el element
WO2004005303A1 (en) * 2002-07-02 2004-01-15 Ferro Corporation Benzene phosphinic acid with improved flowability
JP3885150B2 (en) * 2000-05-17 2007-02-21 ダイニック株式会社 Hygroscopic molded body
JP2011142099A (en) * 2001-01-12 2011-07-21 Nihon Gore Kk Porous adsorbing sheet made of polytetrafluoroethylene
JP2014193454A (en) * 2013-02-26 2014-10-09 Nippon Valqua Ind Ltd Adsorption sheet, manufacturing method for obtaining the adsorption sheet, recovery method of adsorption performance and adsorption method
JP2017170375A (en) * 2016-03-24 2017-09-28 花王株式会社 Composite water-absorbing polymer, and sanitary item containing the same
JP2018187544A (en) * 2017-04-28 2018-11-29 株式会社デンソー Adsorbent and adsorber including adsorbent
JP6466014B1 (en) * 2018-07-26 2019-02-06 株式会社アトムワーク Clothing having a thermal buffer composition and a moisture-containing composition
JP2020006313A (en) * 2018-07-06 2020-01-16 富士電機株式会社 Moisture adsorbent

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52107042A (en) * 1976-03-05 1977-09-08 Japan Synthetic Rubber Co Ltd Hygroscopic composition
JPS56155637A (en) * 1980-05-07 1981-12-01 Hodaka Kagaku Kk Production of brick composed of granular active agent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52107042A (en) * 1976-03-05 1977-09-08 Japan Synthetic Rubber Co Ltd Hygroscopic composition
JPS56155637A (en) * 1980-05-07 1981-12-01 Hodaka Kagaku Kk Production of brick composed of granular active agent

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63264125A (en) * 1987-04-18 1988-11-01 Kobe Steel Ltd Dry dehumidifying component
JP3885150B2 (en) * 2000-05-17 2007-02-21 ダイニック株式会社 Hygroscopic molded body
JP2002280166A (en) * 2001-01-12 2002-09-27 Japan Gore Tex Inc Organic el element
JP2011142099A (en) * 2001-01-12 2011-07-21 Nihon Gore Kk Porous adsorbing sheet made of polytetrafluoroethylene
WO2004005303A1 (en) * 2002-07-02 2004-01-15 Ferro Corporation Benzene phosphinic acid with improved flowability
JP2014193454A (en) * 2013-02-26 2014-10-09 Nippon Valqua Ind Ltd Adsorption sheet, manufacturing method for obtaining the adsorption sheet, recovery method of adsorption performance and adsorption method
JP2017170375A (en) * 2016-03-24 2017-09-28 花王株式会社 Composite water-absorbing polymer, and sanitary item containing the same
JP2018187544A (en) * 2017-04-28 2018-11-29 株式会社デンソー Adsorbent and adsorber including adsorbent
JP2020006313A (en) * 2018-07-06 2020-01-16 富士電機株式会社 Moisture adsorbent
JP6466014B1 (en) * 2018-07-26 2019-02-06 株式会社アトムワーク Clothing having a thermal buffer composition and a moisture-containing composition
WO2020022435A1 (en) * 2018-07-26 2020-01-30 株式会社アトムワーク Thermal buffer composition and clothing including water-containing composition
JP2020015840A (en) * 2018-07-26 2020-01-30 株式会社アトムワーク Clothing having heat buffer composition and moisture-containing composition

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