JPS63110223A - Anti-sweating material - Google Patents
Anti-sweating materialInfo
- Publication number
- JPS63110223A JPS63110223A JP25387186A JP25387186A JPS63110223A JP S63110223 A JPS63110223 A JP S63110223A JP 25387186 A JP25387186 A JP 25387186A JP 25387186 A JP25387186 A JP 25387186A JP S63110223 A JPS63110223 A JP S63110223A
- Authority
- JP
- Japan
- Prior art keywords
- activated carbon
- polymer
- water
- polyurethane
- dew condensation
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 59
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical class [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 62
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 47
- 238000010521 absorption reaction Methods 0.000 claims abstract description 30
- 229920000642 polymer Polymers 0.000 claims abstract description 29
- 239000000835 fiber Substances 0.000 claims abstract description 27
- 229920002635 polyurethane Polymers 0.000 claims abstract description 24
- 239000004814 polyurethane Substances 0.000 claims abstract description 24
- 239000002245 particle Substances 0.000 claims abstract description 14
- 238000009833 condensation Methods 0.000 claims description 29
- 230000005494 condensation Effects 0.000 claims description 25
- 230000002265 prevention Effects 0.000 claims description 21
- 229920006158 high molecular weight polymer Polymers 0.000 claims description 13
- 230000035699 permeability Effects 0.000 abstract description 14
- 238000004898 kneading Methods 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000003495 polar organic solvent Substances 0.000 abstract description 3
- 238000001179 sorption measurement Methods 0.000 abstract 1
- 239000004744 fabric Substances 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- 238000000576 coating method Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- 239000005871 repellent Substances 0.000 description 8
- 230000002940 repellent Effects 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000004677 Nylon Substances 0.000 description 4
- -1 acrylic ester Chemical class 0.000 description 4
- 230000015271 coagulation Effects 0.000 description 4
- 238000005345 coagulation Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000001877 deodorizing effect Effects 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 229920006264 polyurethane film Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000012982 microporous membrane Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000011527 polyurethane coating Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は高分子重合体を主体とするシート状物でありな
がら、結露防止性を有し、かつ透湿性、吸湿性、吸水性
、防水性のある衣料用の防寒衣および雨衣等に適した結
露防止材に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention is a sheet-like material mainly made of a high molecular weight polymer, but it has dew condensation prevention properties, and has moisture permeability, hygroscopicity, water absorbency, and waterproofing properties. The present invention relates to a dew-preventing material suitable for cold weather clothing, rain clothing, etc.
[従来の技術]
従来より各種の防水性コーティング布帛が提案され、実
用に供されている。特に安価で比較的製法の簡単な、た
とえば塩化ビニル、合成ゴム、アクリル酸エステル樹脂
、ウレタン樹脂、アミノ酸樹脂などを布帛状のIIl維
基材に被覆した防水性コーティング布帛がレインコート
などの防水衣料用途に使用されている。しかしながら、
これらの基材は防水性については一応の効果を示すもの
の、衣服として着用した時に、ムレによる不快感を与え
、またテントなどは使用時にその内部に水蒸気が凝結し
、水滴が天井から落るなどの欠点がある。[Prior Art] Various waterproof coated fabrics have been proposed and put into practical use. In particular, waterproof coating fabrics that are inexpensive and relatively easy to manufacture, such as vinyl chloride, synthetic rubber, acrylic ester resins, urethane resins, amino acid resins, etc. coated on fabric-like III fiber base materials, are used for waterproof clothing such as raincoats. used in however,
Although these base materials are somewhat effective in terms of waterproofness, when worn as clothing, they cause discomfort due to stuffiness, and when used in tents, water vapor condenses inside the tent, causing water droplets to fall from the ceiling. There are drawbacks.
一方着用時のむれを軽減するために透湿性を強調した防
水性布帛として、特公昭60−47954、特公昭60
−47955等にみられる透)♀性、防水性コーティン
グ布帛が提案され、実用に供されている。しかしこれら
の基材は透湿性や防水性について一応の効果を奏しては
いるものの、衣服として外気温の低いときに着用した場
合、衣服内の暖かい側、すなわちコーテイング膜面に水
滴が付着するいわゆる結露現象が発生するという欠点が
ある。On the other hand, as a waterproof fabric that emphasizes moisture permeability to reduce stuffiness when worn, Tokuko Sho 60-47954,
Transparent, waterproof coated fabrics such as those found in -47955 have been proposed and put into practical use. However, although these base materials have some effect in terms of moisture permeability and waterproofness, when worn as clothing when the outside temperature is low, water droplets may adhere to the warm side of the clothing, that is, the surface of the coating film. There is a drawback that condensation occurs.
[発明が解決しようとする問題点]
本発明の目的は上述した従来技術の欠点を改善し、高分
子重合体を主体とする素材でありながら、結露防止性を
有し、かつ透湿性、吸湿性、吸水性、防水性のある結露
防止剤を提供することにある。[Problems to be Solved by the Invention] The purpose of the present invention is to improve the above-mentioned drawbacks of the prior art, and to improve the above-mentioned drawbacks of the prior art, it is possible to use a material that is mainly made of a high molecular weight polymer, but has dew condensation prevention properties, moisture permeability, and moisture absorption. The purpose of the present invention is to provide an anti-condensation agent that has excellent water absorption, water absorption, and waterproof properties.
E問題点を解決するための手段]
本発明は上述した目的を達成するため、次のような構成
を有する。すなわち、
(1)活性炭粉末が10〜200重量%混線された高分
子重合体シートであって、かつ吸湿率が5.0%以上(
20℃、90%RH)で、吸水率が5.0%以上である
結露防止材。Means for Solving Problem E] In order to achieve the above-mentioned object, the present invention has the following configuration. That is, (1) A polymer sheet in which 10 to 200% by weight of activated carbon powder is mixed, and the moisture absorption rate is 5.0% or more (
An anti-condensation material having a water absorption rate of 5.0% or more at 20°C and 90% RH.
(2) 活性炭粉末が、粒子径が40〜250μでめ
る特許請求の範囲第(1)項記載の結露防止材。(2) The dew condensation prevention material according to claim (1), wherein the activated carbon powder has a particle size of 40 to 250 μm.
(3) 高分子重合体シートが、繊維基材に積層され
ていることを特徴とする特許請求の範囲第(1)項記載
の結露防止材。(3) The dew condensation prevention material according to claim (1), wherein the polymer sheet is laminated on a fiber base material.
(4)高分子重合体がポリウレタン重合体である特許請
求の範囲第(1)項記載の結露防止材。(4) The dew condensation prevention material according to claim (1), wherein the high molecular weight polymer is a polyurethane polymer.
(5) 高分子重合体シートが、結露水分量3 Mm
2・分以下である特許請求の範囲第(1)項記載の結露
防止材である。(5) The polymer sheet has a condensed moisture content of 3 Mm.
The dew condensation prevention material according to claim (1) has a dew condensation prevention material of 2 minutes or less.
本発明に使用する高分子重合体としては、合成ゴム、ポ
リウレタン、ポリテトラフルオロエチレン、シリコーン
樹脂、ポリエチレン、ポリプロピレン、ポリ塩化ビニル
、ポリアクリル酸エステル樹脂、アミノ酸樹脂等の高分
子重合体が適用できるが、特にポリウレタンが最適であ
る。As the high molecular weight polymer used in the present invention, high molecular weight polymers such as synthetic rubber, polyurethane, polytetrafluoroethylene, silicone resin, polyethylene, polypropylene, polyvinyl chloride, polyacrylic acid ester resin, and amino acid resin can be used. However, polyurethane is particularly suitable.
このポリウレタンとしてはポリエステル系またはポリエ
ーテル系のものが好ましく、一般に乾式または湿式凝固
法によって皮膜に形成することができる。The polyurethane is preferably polyester-based or polyether-based, and can generally be formed into a film by dry or wet coagulation.
また、高分子重合体に混練する粉末状の活性炭としでは
、おが屑、ヤシ殻、石炭などを主体として得られるもの
が使用可能である。Furthermore, as the powdered activated carbon to be kneaded into the high molecular weight polymer, those obtained mainly from sawdust, coconut shells, coal, etc. can be used.
粉末粒子の大きさは、高分子重合体をシート状に形成し
た際、凸凹を持った皮膜表面にすることが好ましく、粒
径は40μより大きく250μより細かいものが良い。Regarding the size of the powder particles, when the high molecular weight polymer is formed into a sheet, it is preferable that the film surface has an uneven surface, and the particle size is preferably larger than 40 μm and finer than 250 μm.
より好ましくは粒径60μより100μからなるものが
良い。粒径40μより細かい場合は、粒子が細かすぎる
ため、合成重合体をシート状の皮膜に形成したとき、表
面の凸凹が出にくく鏡面状態となるため、好ましくない
。More preferably, the particle size is 100μ rather than 60μ. If the particle size is smaller than 40 μm, the particles are too fine, and when the synthetic polymer is formed into a sheet-like film, the surface becomes difficult to have unevenness and becomes mirror-like, which is not preferable.
また粒径が250μより大きい場合は、粒子が大きすぎ
るため、合成重合体をシート状に膜形成したとき、厚さ
が不揃いになりやすく、また活性炭粉末が膜から飛び出
して他の物体と擦られた時に剥離したり、膜が破れたり
、あるいはその他の物体を傷つけたり、汚したすること
があるため好ましくない。In addition, if the particle size is larger than 250μ, the particles are too large, and when the synthetic polymer is formed into a sheet-like film, the thickness tends to be uneven, and the activated carbon powder may jump out of the film and rub against other objects. This is undesirable because it may peel off, the film may tear, or it may damage or stain other objects.
活性炭は吸湿率31.7%(20℃、90%RH)と高
い吸湿性に加えて、吸水性、脱臭性を有しており、綿繊
維の吸湿率が10〜12%(20°C190%R旧で必
るのに比べて著しく高い特性を有している。Activated carbon has a high moisture absorption rate of 31.7% (20℃, 90% RH), as well as water absorption and deodorizing properties. It has characteristics that are significantly higher than those required in the old R.
本発明では、この活性炭を粉末状にして高分子重合体に
混練しシート状に形成させることにより、その高分子重
合体が本来有する防水性や透湿性を低下させることなく
、結露防止性、吸湿性、吸水性を与えることができるよ
うになる。In the present invention, this activated carbon is powdered and kneaded with a polymer to form a sheet, thereby preventing dew condensation and moisture absorption without reducing the waterproofness and moisture permeability inherent to the polymer. It becomes possible to impart properties and water absorption properties.
この活性炭粉末の高分子重合体に対する混練比は、10
〜200重量%、さらに好ましくは30〜150重量%
であることが好ましい。10重伍%より少ない場合は吸
湿性が綿繊維の水準より低下するようになり、また20
0重量%より多い場合は高分子重合体を繊維基材などの
表面に皮膜状にコーティングするとき、その皮膜が剥離
、脱落しやすくなる。The kneading ratio of this activated carbon powder to the high molecular weight polymer was 10
~200% by weight, more preferably 30-150% by weight
It is preferable that If it is less than 10% by weight, the hygroscopicity will be lower than the level of cotton fiber, and if it is less than 20% by weight,
When the amount is more than 0% by weight, when coating the surface of a fiber base material with a high molecular weight polymer in the form of a film, the film is likely to peel off or fall off.
また本発明において、活性炭粉末を混練するに必たり、
他の吸水剤(アニオン系界面活性剤など)、脱臭剤、香
料などを混合するようにしてもよい。In addition, in the present invention, when kneading activated carbon powder,
Other water absorbing agents (such as anionic surfactants), deodorizing agents, fragrances, etc. may be mixed.
本発明において、前記活性炭含有高分子重合体シートは
、吸湿率が5,0%以上、好ましくは6.0%以上(2
0’C,90%RH)であり、かつ吸水率が5゜03以
上であることが重要である。In the present invention, the activated carbon-containing polymer sheet has a moisture absorption rate of 5.0% or more, preferably 6.0% or more (2.
It is important that the temperature is 0'C, 90% RH) and the water absorption rate is 5°03 or more.
本発明の高分子重合体シートは非多孔質でもよいが、好
ましくは微多孔質であるのが透湿性の上から選択される
。活性炭が透湿性、吸湿性、吸水性に対して相乗的に作
用する。The polymer sheet of the present invention may be non-porous, but microporous is preferably selected from the viewpoint of moisture permeability. Activated carbon acts synergistically on moisture permeability, hygroscopicity, and water absorption.
いずれにしても、結露防止作用を大きく向上するために
は、上記吸湿性と吸水性を満足する構成を選択する必要
がある。In any case, in order to greatly improve the dew condensation prevention effect, it is necessary to select a structure that satisfies the above-mentioned hygroscopicity and water absorption.
本発明の高分子重合体シートは、結露水分量が3 Mm
・分以下、好ましくは2 (]/m2・分以下であ
るものが、水滴の生成性の上から選択される。上記範囲
を越える結露水分量を有する場合は衣服や肌にヌレが生
じ易くなるので好ましくない。The polymer sheet of the present invention has a condensed water content of 3 Mm.
・Minutes or less, preferably 2 (]/m2・minutes or less, is selected based on the ability to form water droplets. If the amount of condensed water exceeds the above range, it tends to cause wetness on clothes and skin. So I don't like it.
また活性炭粉末を混練した高分子重合体は、それ単独で
微多孔を有するシート状物に形成して使用するようにし
てもよいが、好ましくは編織物、不織布などの布帛状と
した、繊維基材の表面に皮膜状にコーティングして使用
するのがよい。The high molecular weight polymer kneaded with activated carbon powder may be used by itself in the form of a microporous sheet, but it is preferably used in the form of a fabric such as a knitted fabric or a nonwoven fabric. It is best to use it by coating the surface of the material in the form of a film.
第1図は本発明に係る結露防止材の断面図である。第1
図において、結露防止材1は布帛状の繊維基材2の表面
に活性炭粉末3を混練した高分子重合体を皮膜4として
コーティングさせたものである。このコーティングによ
る皮膜は繊維基材2の両面に設けるようにしてもよい。FIG. 1 is a sectional view of the dew condensation prevention material according to the present invention. 1st
In the figure, a dew condensation prevention material 1 is made by coating the surface of a fabric-like fiber base material 2 with a film 4 of a high molecular weight polymer kneaded with activated carbon powder 3. This coating film may be provided on both sides of the fiber base material 2.
このように繊維基材2と皮膜4を複合させることにより
高分子重合体皮膜の引張強度や引裂強度が補強され、そ
の用途を著しく拡大することができるようになる。By combining the fiber base material 2 and the film 4 in this manner, the tensile strength and tear strength of the polymer film are reinforced, and its uses can be significantly expanded.
高分子重合体としてポリウレタン重合体を使用し、これ
を繊維基材にコーティングする方法を代表させて、以下
本発明の結露防止材を製造する方法の一例を説明する。An example of a method for manufacturing the dew condensation prevention material of the present invention will be described below, using a polyurethane polymer as a high molecular weight polymer and using a typical method of coating a fiber base material with the polyurethane polymer.
第一工程:繊維基材に対する活性炭粉末を混練したポリ
ウレタン重合体溶液の浸透が、繊維基材の厚さのに以下
に抑制するため、及び基材に旧水性機能を付与するため
の処理をあらかじめ後述のような処理を施す。First step: In order to suppress the penetration of the polyurethane polymer solution mixed with activated carbon powder into the fiber base material to less than the thickness of the fiber base material, and to give the base material a water-based function. Perform processing as described below.
第二工程:活性炭粉末を混合したポリウレタン重合体を
主体として含有する極性有機溶剤溶液を、前記第−工程
俊の繊維基材の少なくとも片面に塗布する。Second step: A polar organic solvent solution mainly containing a polyurethane polymer mixed with activated carbon powder is applied to at least one side of the fiber base material of the first step.
第三工程:第二工程後のシート状物を凝固液中に浸漬し
、活性炭を含有したポリウレタン微多孔性皮膜を形成さ
せる。Third step: The sheet material after the second step is immersed in a coagulation liquid to form a microporous polyurethane film containing activated carbon.
本発明では、第一工程を省略し、第二工程、第三工程を
実施するようにしてもよいが、吸湿性、透湿性を向上さ
せると共にコーティング布帛の風合を改良するためには
、第一工程の前処理を施すことが望ましい。この前処理
手段としては、繊維基材の表面でかつ活性炭含有ポリウ
レタン重合体溶液を塗布する面を加熱加圧して繊維の断
面形状を変形し、繊維間隙を狭くしておく方法、繊維基
材にシリコーン系あるいは弗素系などの撥水剤を施す方
法などがある。さらに接着性を改善するために下引きア
ンダーコートすることも好ましい。In the present invention, the first step may be omitted and the second and third steps may be carried out, but in order to improve the moisture absorption and moisture permeability as well as the feel of the coated fabric, the It is desirable to perform a one-step pretreatment. As a pretreatment method, the surface of the fiber base material and the surface to which the activated carbon-containing polyurethane polymer solution is applied is heated and pressurized to change the cross-sectional shape of the fibers and narrow the fiber gaps. There are methods of applying water repellents such as silicone-based or fluorine-based water repellents. It is also preferable to apply a subbing undercoat to further improve adhesion.
そしてこれらの前処理手段を繊維基材に適宜施すことに
より、活性炭含有ポリウレタン重合体溶液の塗布にあた
り、該重合体溶液の繊維基材に対する浸透を抑制すると
同時に該繊維基材を構成する繊維と合成重合体との結合
を弛緩する、従って、それによって風合が柔軟で吸湿性
、透湿性に富んだ活性炭含有樹脂コーティング布帛を得
ることができる。By appropriately applying these pretreatment means to the fiber base material, when applying the activated carbon-containing polyurethane polymer solution, it is possible to suppress the permeation of the polymer solution into the fiber base material, and at the same time to inhibit the synthesis with the fibers constituting the fiber base material. By relaxing the bond with the polymer, it is possible to obtain an activated carbon-containing resin-coated fabric that has a soft feel and is highly hygroscopic and moisture permeable.
なお、活性炭含有ポリウレタン重合体溶液が繊維基材の
厚さ方向に、その厚さの3分の1以上浸透していると、
浸透度、引裂強度などの物性や柔軟性が低下するように
なる。In addition, if the activated carbon-containing polyurethane polymer solution penetrates into the fiber base material in the thickness direction, one-third or more of the thickness of the fiber base material,
Physical properties such as permeability and tear strength, as well as flexibility, begin to decline.
また、上述の製造方法に使用するポリウレタン重合体溶
液の組成は、ポリウレタン重合体8〜25重量%を含有
するジメチルホルムアミドによって代表される極性有機
溶媒溶液に、弗素系撥水剤0.1〜1.0重量%、ポリ
イソシアネート類0゜2〜3重量%および非イオン界面
活性剤1〜10重量%を配合したものが好ましい。この
調合液に前記活性炭をポリウレタン重合体に対し10及
至200重量%混合し、湿式凝固法によって生成する。The composition of the polyurethane polymer solution used in the above manufacturing method is as follows: A polar organic solvent solution represented by dimethylformamide containing 8 to 25% by weight of the polyurethane polymer, and 0.1 to 1 to 1% of the fluorine-based water repellent. 0.0% by weight, 0.2 to 3% by weight of polyisocyanates, and 1 to 10% by weight of a nonionic surfactant. 10 to 200% by weight of the activated carbon based on the polyurethane polymer is mixed into this liquid mixture, and the mixture is produced by a wet coagulation method.
上記調合液の塗布方法としては、ナイフオーバーロール
コータ−その他通常のコーテイング機を使用し、任意の
厚さに均一に塗布する。The above-mentioned liquid mixture is coated uniformly to a desired thickness using a knife-over-roll coater or other ordinary coating machine.
・第三工程についてはとくに限定されないが、凝固浴と
してジメチルホルムアミド5及至15重1%を含有する
水溶液を用いるのが有利である。- The third step is not particularly limited, but it is advantageous to use an aqueous solution containing 5 to 15% by weight of dimethylformamide as the coagulation bath.
[実施例] 実施例において用いる評価項目について説明する。[Example] Evaluation items used in Examples will be explained.
(1) 皮膜の表面の凹凸:膜断面を走査型電子顕微
鏡で150倍の写真を取り、この写真上の直線10cm
間における膜表面に相当する断面の軌跡の長さを測定し
て表わした。(1) Irregularities on the surface of the film: Take a photograph of the cross section of the film at 150x magnification using a scanning electron microscope, and draw a 10cm straight line on the photograph.
The length of the locus of the cross section corresponding to the membrane surface between the two was measured and expressed.
(2)結露水分量:水温60℃の水2000〜4000
ccが入った容器の中に水面から5〜10CIn離し
て、氷の入った箱18X18X5on(タテXヨコX高
さ)を置き、箱の上面に9重9cm(タテXヨコ)の穴
を開け、その穴を寒くようにシート状物(試料>10X
10X10タテXヨコ)を貼り付け、60秒間に結露し
た水分It (A)を次式で測定した。(2) Condensation moisture content: 2,000 to 4,000 water at a water temperature of 60°C
Place an 18 x 18 x 5 on (vertical x horizontal x height) box containing ice at a distance of 5 to 10 CIn from the water surface in a container containing cc, and make 9-fold, 9-cm (vertical x horizontal) holes in the top of the box. Place a sheet of material (sample>10X) to cool the hole.
10×10 vertically and horizontally) was attached, and the moisture It (A) condensed in 60 seconds was measured using the following formula.
結露水分量(A>=B−C
B:60秒間結露させたシート状物総重量C:シート状
物の皮膜の付着水分をろ紙で拭き取った後の重量
(3) 吸湿率:JIS L1096 ただし繊
維基材の素材はポリアミド繊維など、化学、合成繊維で
構成されていること。20℃、90%RH条件下で実施
。Condensed moisture content (A>=B-C B: Total weight of sheet material with dew condensation for 60 seconds C: Weight after wiping off moisture on the film of sheet material with filter paper (3) Moisture absorption rate: JIS L1096 However, fiber The base material must be made of chemical or synthetic fibers such as polyamide fibers.Conducted at 20℃ and 90%RH conditions.
(4) 吸水率:10X10c1n(タテXヨコ〉厚
さ5 mmのダンボール紙に試料10X10X10タテ
Xヨコ)を貼り付け、水深的2〜3 rnmの中に試料
を下にして60秒間浸漬した後の吸水率(X%)を次式
で求めた。(4) Water absorption rate: 10 x 10 c1n (vertical x horizontal) After pasting a sample 10 x 10 x 10 vertical x horizontal on a 5 mm thick cardboard paper and immersing it in water at a depth of 2 to 3 nm with the sample facing down for 60 seconds. The water absorption rate (X%) was determined using the following formula.
吸水率X(%)= (Y−Z)/ZXI00Y:60秒
間浸漬後、ダンボール紙から試料を外し皮膜表面の付着
水分を口紙で
ふき取った後の試料の総重量。Water absorption rate X (%) = (Y-Z)/ZXI00Y: Total weight of the sample after being immersed for 60 seconds, removing the sample from the cardboard paper, and wiping off the moisture adhering to the film surface with a paper towel.
Z:浸漬する前の試料の重囲 (5) 透湿度:JIS Z−0208による。Z: Surrounding of sample before immersion (5) Moisture permeability: According to JIS Z-0208.
(6) 耐水圧:JIS L−1079によった。(6) Water pressure resistance: According to JIS L-1079.
染色されたナイロンタフタ(タテ・ヨコ70dナイロン
フィラメント使い、タテ密度Xヨコ密度=123 x8
7本/インチ)に弗素系撥水剤水分散液を絞り率60%
でパッディング処理し、乾燥熱処理を施す、弗素系撥水
剤の付着量は0.3重量%である。Dyed nylon taffeta (vertical and horizontal 70d nylon filament used, vertical density x horizontal density = 123 x 8
7 bottles/inch) with 60% squeezing rate of fluorine-based water repellent aqueous dispersion
The amount of fluorine-based water repellent applied is 0.3% by weight.
この処理を例えば基材の撥水加工ありとした。For example, this treatment was treated as water-repellent treatment of the base material.
ポリエステル系ポリウレタン溶液100重量部、ポリイ
ソシアネート4重量部、メチルエチルケトン30部より
なる塗料液(粘度6000 cos/25℃)を前期処
理済み生地にナイフフロートコーティング法により付着
ff130g/m2で塗布、乾燥し接着層とした。A coating liquid (viscosity 6000 cos/25°C) consisting of 100 parts by weight of polyester polyurethane solution, 4 parts by weight of polyisocyanate, and 30 parts of methyl ethyl ketone was applied to the previously treated fabric using the knife float coating method at a ff of 130 g/m2, dried and bonded. layered.
なあ、この接着層は布帛状の繊維基材と活性炭を含む微
多孔層を分離し、活性炭が繊維基材を汚染するのを防止
する機能ももつ。Incidentally, this adhesive layer also has the function of separating the fabric-like fiber base material and the microporous layer containing activated carbon, and preventing the activated carbon from contaminating the fiber base material.
次いでポリエステル系ポリウレタン18重量部、ヤシ殻
活性炭(74〜149μ)9重量部、およびジメチルホ
ルムアミド70重量部よりなるポリウレタン塗布液をナ
イフオーバーロールコータ−を用いて150 g/(W
et) 1布した後、ジメチルホルムアミド3重囲%含
む水中に浸漬凝固させ、水洗、急速熱風乾燥して活性炭
を含有した微細気孔を有するシート状物を得た。Next, a polyurethane coating solution consisting of 18 parts by weight of polyester polyurethane, 9 parts by weight of coconut shell activated carbon (74 to 149μ), and 70 parts by weight of dimethylformamide was coated at 150 g/(W) using a knife-over-roll coater.
et) After 1 cloth, it was immersed in water containing 3% dimethylformamide to coagulate, washed with water, and rapidly dried with hot air to obtain a sheet-like material containing activated carbon and having fine pores.
得られた結果を第1表に示す。The results obtained are shown in Table 1.
ただし、水準1は繊維基材としてポリエステル100%
のタフタに撥水カレンダ加工したものを用いた。そして
接着層となるポリウレタン溶液の塗布は行わず、直接活
性炭含有ポリウレタン溶液を塗布、湿式凝固させ、乾燥
させた。しかるのち、タフタとウレタン膜を剥離させて
得たものである。However, level 1 is 100% polyester as the fiber base material.
Taffeta treated with a water-repellent calender was used. Then, a polyurethane solution containing activated carbon was directly applied, wet-coagulated, and dried, without applying a polyurethane solution that would become an adhesive layer. After that, the taffeta and urethane film were peeled off.
なお比較例として次のものを挙げた。The following were listed as comparative examples.
比較例1は前記接着層まで処理した基布にヤシ殻活性炭
を混練しないポリエステル系ポリウレタンのジメチルホ
ルムアミド溶液を実施例と同様に塗布復温式凝固せしめ
て得たものである。Comparative Example 1 was obtained by applying a dimethylformamide solution of polyester polyurethane without kneading coconut shell activated carbon to the base fabric treated to the adhesive layer and coagulating it by reheating in the same manner as in the example.
比較例2はナイロンタフタに微細気孔を有する(湿式処
理による連続気泡)ポリウレタン皮膜をコーティングし
たB社の市販品である。Comparative Example 2 is a commercially available product from Company B in which nylon taffeta is coated with a polyurethane film having fine pores (open cells formed by wet treatment).
比較例3は綿100%の織物である。Comparative Example 3 is a 100% cotton fabric.
第1表から明らかなように、本実施例に係る結露防止材
は比較例1.2の微多孔質皮膜に活性炭を含まないもの
にくらべ、結露水分が少なく、吸湿率、吸水率、および
膜表面の凸凹が大きいという透湿性、防水性、結露防止
性が向上していることを示している。As is clear from Table 1, the dew condensation prevention material according to this example has less condensed water than the microporous film of Comparative Example 1.2, which does not contain activated carbon, and the moisture absorption rate, water absorption rate, and film This indicates that the moisture permeability, waterproofness, and dew condensation prevention properties are improved due to the large unevenness of the surface.
綿100%織物について膜表面の凸凹の大きいのは織物
の糸の凸凹が直接あられれ、他のものはコーティング表
面で偏平になっている点が異なる。For 100% cotton fabrics, the large unevenness on the membrane surface is due to the unevenness of the threads of the fabric being directly formed, whereas the other differences are that the coating surface is flattened.
また綿100%織物の吸湿率、透湿度、吸水率が多きく
、結露水分がOであるのは綿特有の特性であるが、耐水
性がOであり、防水機能はない。In addition, 100% cotton fabric has a high moisture absorption rate, moisture permeability, and water absorption rate, and its condensed moisture is O, which is a characteristic unique to cotton, but its water resistance is O, and it does not have a waterproof function.
[参考例] 第2表に示したものは次の条件で試料を作成した。[Reference example] The samples shown in Table 2 were prepared under the following conditions.
ポリウレタン25重量%を含有するケトン系溶剤溶液に
活性炭の粒径、混線率(対ポリウレタン重量比)をかえ
て投入し、スクリュー型攪拌機で混練した。この混練溶
液をナイロンフィラメント’100%使い織物にナイフ
コータを用いてioo g/、Tr12(Δet)塗布
し、乾燥処理を行ったのち、弗素系撥水剤1重量%含有
する溶液中に浸漬、ヒートセットを行ったのち、コーテ
ィング皮膜面を水洗、急速乾燥を行った。(非微多孔膜
)
第2図は第2表の結果のうち、膜表面の凸凹と結露水分
量の関係を示すグラフである。Activated carbon was added to a ketone solvent solution containing 25% by weight of polyurethane while changing the particle size and cross-mixing ratio (weight ratio to polyurethane), and kneaded with a screw type stirrer. This kneading solution was coated with ioo g/, Tr12 (Δet) using a knife coater on a fabric made of 100% nylon filament. After drying, it was immersed in a solution containing 1% by weight of a fluorine-based water repellent and heated. After setting, the coating film surface was washed with water and quickly dried. (Non-microporous membrane) FIG. 2 is a graph showing the relationship between the unevenness of the membrane surface and the amount of condensed water among the results in Table 2.
第3図は第2表の結果のうち膜表面の凸凹と吸湿率の関
係を示すグラフである。FIG. 3 is a graph showing the relationship between the unevenness of the film surface and the moisture absorption rate among the results shown in Table 2.
第2図からおよび第3図から明らかなように、膜表面の
凸凹が大きくなると結露水分量は減少し、吸湿率は増加
することがわかる。As is clear from FIGS. 2 and 3, it can be seen that as the unevenness of the film surface increases, the amount of condensed water decreases and the moisture absorption rate increases.
第2表からもわかるように、活性炭の粒径が大きくなる
程、また活性炭の混練率が増すほど、膜表面の凸凹は増
大する。As can be seen from Table 2, as the particle size of the activated carbon increases and as the kneading rate of the activated carbon increases, the unevenness of the membrane surface increases.
本実施例において、活性炭の粒径は変化させなかったも
のの、粒径を変化(膜表面の凸凹)させた場合にも同様
の傾向を示すものと推定される。Although the particle size of the activated carbon was not changed in this example, it is presumed that a similar tendency would be exhibited even if the particle size was changed (irregularities on the film surface).
[発明の効果]・
本発明の結露防止材は、上述したように微多孔性高分子
重合体の皮膜により、本来の防水性、透湿性を有するこ
とは勿論、混入された活性炭粉末により高い吸湿性、吸
水性、結露防止性を有するようになる。したがって外気
温の低い時に衣服として着用した場合であっても、その
内側に結露が発生するのを防止、または軽減させること
ができる。[Effects of the invention]- As mentioned above, the dew condensation prevention material of the present invention not only has inherent waterproofness and moisture permeability due to the microporous polymer film, but also has high moisture absorption due to the activated carbon powder mixed in. It has properties such as water absorption, and anti-condensation properties. Therefore, even when worn as clothing when the outside temperature is low, it is possible to prevent or reduce the formation of dew on the inside.
第1図は本発明に係る結露防止材の断面図である。第2
図は第2表の結果のうち、膜表面の凸凹と結露水分量の
関係を示すグラフである。第3図は第2表の結果のうち
、膜表面の凸凹と吸湿量の関係を示すグラフである。
図中
1:結露防止材 2:布帛状の繊維基材3:活性炭粉末
4:被膜FIG. 1 is a sectional view of the dew condensation prevention material according to the present invention. Second
The figure is a graph showing the relationship between the unevenness of the film surface and the amount of condensed water among the results in Table 2. FIG. 3 is a graph showing the relationship between the unevenness of the film surface and the amount of moisture absorption among the results shown in Table 2. In the figure: 1: Condensation prevention material 2: Fabric-like fiber base material 3: Activated carbon powder 4: Coating
Claims (5)
子重合体シートであつて、かつ吸湿率が5.0%以上(
20℃、90%RH)で、吸水率が5.0%以上である
結露防止材。(1) A polymer sheet kneaded with 10 to 200% by weight of activated carbon powder, and having a moisture absorption rate of 5.0% or more (
An anti-condensation material having a water absorption rate of 5.0% or more at 20°C and 90% RH.
許請求の範囲第(1)項記載の結露防止材。(2) The dew condensation prevention material according to claim (1), wherein the activated carbon powder has a particle size of 40 to 250 μm.
ることを特徴とする特許請求の範囲第(1)項記載の結
露防止材。(3) The dew condensation prevention material according to claim (1), wherein the polymer sheet is laminated on a fiber base material.
求の範囲第(1)項記載の結露防止材。(4) The dew condensation prevention material according to claim (1), wherein the high molecular weight polymer is a polyurethane polymer.
・分以下である特許請求の範囲第(1)項記載の結露防
止材。(5) The polymer sheet has a condensed water content of 3g/m^2
The dew condensation prevention material according to claim (1), which has a dew condensation prevention material of less than .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25387186A JPS63110223A (en) | 1986-10-27 | 1986-10-27 | Anti-sweating material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25387186A JPS63110223A (en) | 1986-10-27 | 1986-10-27 | Anti-sweating material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63110223A true JPS63110223A (en) | 1988-05-14 |
Family
ID=17257293
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25387186A Pending JPS63110223A (en) | 1986-10-27 | 1986-10-27 | Anti-sweating material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63110223A (en) |
-
1986
- 1986-10-27 JP JP25387186A patent/JPS63110223A/en active Pending
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