JPH03213535A - Woven or knitted fabric - Google Patents
Woven or knitted fabricInfo
- Publication number
- JPH03213535A JPH03213535A JP2007503A JP750390A JPH03213535A JP H03213535 A JPH03213535 A JP H03213535A JP 2007503 A JP2007503 A JP 2007503A JP 750390 A JP750390 A JP 750390A JP H03213535 A JPH03213535 A JP H03213535A
- Authority
- JP
- Japan
- Prior art keywords
- woven
- knitted fabric
- fabric
- present
- polymer
- 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
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 53
- 229920000642 polymer Polymers 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229920000728 polyester Polymers 0.000 claims abstract description 17
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000005977 Ethylene Substances 0.000 claims abstract description 10
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 5
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 4
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 4
- 239000000835 fiber Substances 0.000 claims description 39
- 238000010521 absorption reaction Methods 0.000 claims description 18
- 238000009792 diffusion process Methods 0.000 claims 1
- -1 polyethylene terephthalate Polymers 0.000 abstract description 18
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 7
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 7
- 238000007127 saponification reaction Methods 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 4
- 239000002759 woven fabric Substances 0.000 abstract description 4
- 230000003578 releasing effect Effects 0.000 abstract 2
- 230000001268 conjugating effect Effects 0.000 abstract 1
- 239000002131 composite material Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 238000009987 spinning Methods 0.000 description 13
- 239000000306 component Substances 0.000 description 11
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 238000010586 diagram Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 238000013329 compounding Methods 0.000 description 5
- 210000004243 sweat Anatomy 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002433 hydrophilic molecules Chemical class 0.000 description 3
- 230000035900 sweating Effects 0.000 description 3
- 229920006230 thermoplastic polyester resin Polymers 0.000 description 3
- 230000004580 weight loss Effects 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- CSPVUHYZUZZRGF-RNFRBKRXSA-N (4R,6R)-hydroxy-2,2,6-trimethylcyclohexanone Chemical compound C[C@@H]1C[C@@H](O)CC(C)(C)C1=O CSPVUHYZUZZRGF-RNFRBKRXSA-N 0.000 description 2
- 229930185327 Actinol Natural products 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical group O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 description 1
- SHSGDXCJYVZFTP-UHFFFAOYSA-N 4-ethoxybenzoic acid Chemical compound CCOC1=CC=C(C(O)=O)C=C1 SHSGDXCJYVZFTP-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 239000007832 Na2SO4 Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Landscapes
- Knitting Of Fabric (AREA)
- Multicomponent Fibers (AREA)
- Woven Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、エチレン酢酸ビニル共重合体のケン化物ポリ
マー(以下エチレンビニルアルコールコポリマーと称す
)と熱可塑性ポリエステル樹脂を混合または複合させた
繊維を用いて得られる吸湿及び放湿性に優れた織編物に
関するものであり、例えばインナー 中表、スポーツ衣
料等の用途に好適に使用することができるものである。Detailed Description of the Invention (Field of Industrial Application) The present invention provides fibers made by mixing or composing a saponified ethylene vinyl acetate copolymer (hereinafter referred to as ethylene vinyl alcohol copolymer) with a thermoplastic polyester resin. This invention relates to a woven or knitted fabric that has excellent moisture absorption and moisture release properties, and can be suitably used for, for example, innerwear, sports clothing, and the like.
(従来の技術)
ポリエステル繊維は、天然繊維には見られない優れた強
度、弾性、耐摩耗性、耐薬品性、耐候性、形態安定性な
ど、そのすぐれた汎用特性により繊維としてきわめて多
量に生産、消費されているが、その反面、肌着やスポー
ツウェアー等の衣料素材としては、疎水性のために、発
汗した汗をすばやく、効果的に吸収して、放散すること
ができないので、発汗時には、衣服内の湿度が上昇し、
むれ感や、肌のぬれ等の不快感を生ずるという欠点があ
る。(Conventional technology) Polyester fibers are produced in extremely large quantities as fibers due to their excellent general-purpose properties such as excellent strength, elasticity, abrasion resistance, chemical resistance, weather resistance, and morphological stability that are not found in natural fibers. However, on the other hand, as clothing materials such as underwear and sportswear, due to their hydrophobic nature, they cannot quickly and effectively absorb and dissipate sweat, so when sweating, The humidity inside the clothes increases,
It has the disadvantage of causing discomfort such as stuffiness and wet skin.
(発明が解決しようとする課題)
このような欠点を改善すべく、ポリエステル繊維の親水
化が多方面に亘り研究されている。例えば、親水性化合
物をポリエステルにグラフト重合させる手法が試みられ
ているが、親水性化合物を多量に導入すれば、繊維基材
の本来の性質が損ねられ、実用に供し得ないものとなる
し、一方、親水性化合物を減少させれば十分な親水性は
得られず、発汗時の不快感は解消されない。ゆえに、単
なる共重合等によるポリマー改質には限界があり、依然
として、肌着や、スポーツウェアー等の衣料素材として
は十分に改善されていないのが実情である。(Problems to be Solved by the Invention) In order to improve these drawbacks, various studies have been conducted on making polyester fibers hydrophilic. For example, attempts have been made to graft-polymerize a hydrophilic compound onto polyester, but if a large amount of hydrophilic compound is introduced, the original properties of the fiber base material will be impaired, making it impractical. On the other hand, if the amount of hydrophilic compounds is reduced, sufficient hydrophilicity cannot be obtained and discomfort during sweating cannot be alleviated. Therefore, there are limits to polymer modification through simple copolymerization, and the reality is that it has not yet been sufficiently improved as a material for clothing such as underwear and sportswear.
(課題を解決するための手段)
本発明者等は、上記の問題点を解決すべく研究を行なっ
た結果、本発明に到達した。すなわち本発明は、エチレ
ン含量が30〜70モル%のエチレンビニルアルコール
コポリマー(A)と熱可塑性ポリエステル系ポリマー(
B)が重量比率(A) : (B)−5:95〜60:
40の範囲で合わされた単繊維繊度5デニール以下の多
成分系繊維からなる織編物であって、該織編物が次の吸
湿率(X)および吸水放散速度(Y)
X > 1.5%
Y > 1.5%/分
を満足することを特徴とする織編物である。(Means for Solving the Problems) The present inventors conducted research to solve the above problems, and as a result, they arrived at the present invention. That is, the present invention comprises an ethylene vinyl alcohol copolymer (A) having an ethylene content of 30 to 70 mol% and a thermoplastic polyester polymer (
B) has a weight ratio of (A): (B)-5:95 to 60:
A woven or knitted fabric made of multicomponent fibers with a single fiber fineness of 5 deniers or less combined in the range of 40, the woven or knitted fabric having the following moisture absorption rate (X) and water absorption/dissipation rate (Y) X > 1.5% Y >1.5%/min.
(作 用)
以下、図面等に基づいて、さらに詳しく、本発明の織編
物について説明する。(Function) Hereinafter, the woven or knitted fabric of the present invention will be explained in more detail based on the drawings and the like.
本発明の織編物は、好ましくは、ケン化度95モル%以
上にしてエチレン成分含量が30〜70モル%のエチレ
ンビニルアルコール系コポリマーと熱可塑性ポリエステ
ル樹脂が重量比率5:95〜60:40の範囲で混合ま
たは複合された繊維から成る織編物で、該織編物を構成
する繊維の、単繊維の繊度が5デニール以下で、該織編
物の厚さが1mm以下、目付250g/m’以下である
織編物であって、該織編物が1.5%<X、1.5%/
分〈Yを満足することを特徴とする吸湿及び放湿性にす
ぐれた織編物である。The woven or knitted fabric of the present invention preferably contains an ethylene vinyl alcohol copolymer with a saponification degree of 95 mol% or more and an ethylene component content of 30 to 70 mol% and a thermoplastic polyester resin in a weight ratio of 5:95 to 60:40. A woven or knitted fabric made of fibers mixed or composited within a range, where the single fiber fineness of the fibers constituting the woven or knitted fabric is 5 denier or less, the thickness of the woven or knitted fabric is 1 mm or less, and the basis weight is 250 g/m' or less. A certain woven or knitted fabric, the woven or knitted fabric has 1.5%<X, 1.5%/
This is a woven or knitted fabric with excellent moisture absorption and moisture release properties, which satisfies the condition <Y.
本発明で言うXは絶乾状態から、20℃×85%RHへ
の吸湿率(%)を示し、これは、発汗時に生ずるむれ感
等の着心地に影響を及ぼすものである。In the present invention, X indicates the moisture absorption rate (%) from an extremely dry state to 20° C. x 85% RH, which affects the comfort of the wearer, such as the feeling of stuffiness that occurs when sweating.
すなわち、吸湿率Xが1.5%以下であると、衣服がほ
とんど吸湿しないので、発汗した気体状の汗を効果的に
外部に発散できず、着心地の向上は期持
・できない。Yは、20℃×65%RH環境下で、ポリ
エチレンフィルム上に一定量の水滴をのせ、その上に該
織編物をのせた時の織編物の吸水放散速度を示すもので
あり、肌に直に接する衣服が、発汗した汗を吸水し、布
帛内部で拡散しながら、蒸発、乾燥する状態をシミュレ
ートするものである。That is, if the moisture absorption rate X is 1.5% or less, the clothing hardly absorbs moisture, so the gaseous sweat cannot be effectively released to the outside, and the comfort cannot be expected to improve. Y indicates the water absorption and dissipation rate of the woven or knitted fabric when a certain amount of water droplets are placed on a polyethylene film and the woven or knitted fabric is placed on top of it in an environment of 20°C x 65% RH. This simulates the situation in which clothing in contact with the fabric absorbs sweat and evaporates and dries as it diffuses inside the fabric.
Yが1.5%/分以下であると、発汗した汗が皮膚に溜
り、衣服の濡れ時間も長くなるので、べとつき感や湿潤
感等の不快感が持続し、好ましくない。If Y is less than 1.5%/min, sweat accumulates on the skin and the time the clothes are wet becomes longer, resulting in persistent unpleasant sensations such as stickiness and dampness, which is not preferable.
さらにこのようなXおよびYを満足するためには、該織
編物の厚さが1mm以下、目付250g/m’以下であ
ることが好ましく、モして該織編物を構成する繊維の単
繊維の繊度が5デニール以下であることが必要である。Furthermore, in order to satisfy X and Y, the thickness of the woven or knitted fabric is preferably 1 mm or less and the basis weight is 250 g/m' or less, and the monofilament of the fibers constituting the woven or knitted fabric is preferably It is necessary that the fineness is 5 denier or less.
該織編物の厚さが1mmを越えると、織編物が吸水して
も、水分を効果的に放散することができず好ましくない
。すなわち、Yの測定において、吸水された水分は、厚
さ方向にはすばやく移動するが、横方向には広がらない
ため、吸水放散速度Yが十分には満足されず、目的とす
るすぐれた汗処理効果は得られない。また、目付が25
0g/m2を越えると、当然厚さも厚くなり、前述の理
由により好ましくない。該織編物を構成する繊維の、単
繊維の繊度が5drを越えると、織編物が吸水しても、
水分の蒸発面積が絶対的に小さいため、Yが満足されず
肌のぬれが持続し、好ましくない。If the thickness of the woven or knitted fabric exceeds 1 mm, even if the woven or knitted fabric absorbs water, the water cannot be effectively dissipated, which is not preferable. In other words, when measuring Y, absorbed water moves quickly in the thickness direction, but does not spread in the lateral direction, so the water absorption and dissipation rate Y is not fully satisfied, and the desired excellent sweat treatment is not achieved. No effect will be obtained. Also, the basis weight is 25
If it exceeds 0 g/m2, the thickness will naturally increase, which is not preferable for the reasons mentioned above. If the single fiber fineness of the fibers constituting the woven or knitted fabric exceeds 5 dr, even if the woven or knitted fabric absorbs water,
Since the area for water evaporation is absolutely small, Y is not satisfied and the skin remains wet, which is not preferable.
本発明でいう厚さ、目付はJ I S L 1096
に準拠した次の方法で測定される。厚さの測定は、試料
の5ケ所以上について、一定時間、一定圧力のもとで、
厚さが落ちついてから測定し、その平均値で示す。この
一定時間とは、一般には10秒間をいい、一定圧力とは
、JISに規定された圧力であり、例えば、普通の織物
では、240g/cm2、普準状態で24時間以上調湿
し、重量を測り、その平均値を1m2当りの重量に換算
する。The thickness and basis weight in the present invention are JIS L 1096.
Measured using the following method in accordance with The thickness is measured at 5 or more locations on the sample for a certain period of time under a certain pressure.
Measurements are taken after the thickness has settled down, and the average value is shown. This fixed time generally refers to 10 seconds, and the fixed pressure is the pressure specified in JIS. Measure and convert the average value to the weight per 1 m2.
次に本発明でいうXの測定は、10cmX loam以
上の試験片を採取し、その絶乾重量(W、)と、温度2
0℃、湿度85%RHに調湿された容器内に、かかる試
験片を放置し、試験片が十分に調湿された時の重量(W
)を測定し、以下の式を用いて、Xの値を算出する。Next, the measurement of X in the present invention involves taking a test piece of 10 cm x loam or more, and measuring its absolute dry weight (W) and temperature 2.
The test piece was left in a container whose humidity was adjusted to 0°C and 85% RH, and the weight (W
) is measured, and the value of X is calculated using the following formula.
また本発明でいう織編物の吸水放散速度Yの測定は下記
■〜■の手順で試験を行なうものである。Furthermore, the water absorption/dissipation rate Y of the woven or knitted fabric as referred to in the present invention is measured by testing according to the following procedures (1) to (4).
■ 試験片を10cmX Loamに裁断する。■ Cut the test piece into 10cm x loam pieces.
■ 採取した試験片を温度20 ’C1C10o±5%
RHの環境下で5時間以上放置して平衡状態にする。■ The sampled test piece was heated to a temperature of 20'C1C10o±5%.
Leave it in an RH environment for 5 hours or more to reach an equilibrium state.
■ 20℃、60±5%環境下において、元の重量とし
て、ポリエチレンフィルムと試験片を天秤を用いて測定
した後、ポリエチレンフィルム上に20±2℃の蒸留水
1gを正確に秤量する。(2) Measure the original weight of the polyethylene film and test piece using a balance in an environment of 20°C and 60±5%, and then accurately weigh 1 g of distilled water at 20±2°C onto the polyethylene film.
■ Igの蒸留水をのせたポリエチレンフィルムを平ら
なアルミバットに移し、その上に試験片をかぶせて放置
し時刻を測る。■ Transfer the polyethylene film containing Ig distilled water to a flat aluminum vat, cover it with the test piece, leave it to stand, and measure the time.
■ 次いで3°、5°、 10’、 20’、・・・・
・60′、・・・・・と順次時間経過毎にアルミバット
を除く全型−
量を秤量して、水分残存量を求める。■ Then 3°, 5°, 10', 20', etc.
・60', etc. Weigh the entire mold except for the aluminum bat as time passes and determine the amount of remaining moisture.
■ 注水した蒸留水1gを100とし、時間毎の水分残
存重量を%で示して、減量カーブをプロットする。(1) Taking 1 g of the distilled water poured as 100, plot the weight loss curve by showing the residual weight of water per hour in %.
■ 水分残存重量が100%から10%まで減少するの
に要する時間より、織編物の吸水放散速度Yを算出する
。(2) Calculate the water absorption/dissipation rate Y of the woven or knitted fabric from the time required for the residual moisture weight to decrease from 100% to 10%.
本発明の織編物は、いかなる組織でも良く、例えば、平
織、綾織、朱子織、平編、ゴム編、パール編、鎖編、デ
ンビー編、コード編、インレイ編、アトラス編等あげら
れるが、これに限定されるものでない。また、かかる織
編物は、100%が該混合または複合繊維である必要は
なく、他の天然あるいは合成繊維との混繊糸、交わん糸
、あるいは、交織、交編物であってもよい。The woven or knitted fabric of the present invention may have any structure, such as plain weave, twill weave, satin weave, plain knit, rubber knit, purl knit, chain knit, Denby knit, cord knit, inlay knit, atlas knit, etc. It is not limited to. Furthermore, such a woven or knitted fabric does not need to be made up of 100% of the mixed or composite fibers, but may be a blended yarn, interlaced yarn, or interwoven or interwoven fabric with other natural or synthetic fibers.
次に本発明の織編物の構成をさらに詳しく説明する。Next, the structure of the woven or knitted fabric of the present invention will be explained in more detail.
本発明でいう熱可塑性ポリエステル樹脂とは、例えば、
テレフタール酸、イソフタル酸、ナフタリン2.6−ジ
カルボン酸、フタール酸、α、β−8
(4−カルボキシフェノキシ)エタン、4.4°−ジカ
ルボキシジフェニル、5−ナトリウムスルホンイソフタ
ル酸などの芳香族ジカルボン酸、または、これらのエス
テル類とエチレングリコール、ジエチレングリコール、
■、4°−ブタンジオール、ネオペンチルグリコール、
シクロヘキサン、1.4’−ジメタツール、ポリエチレ
ングリコール、ポリテトラメチレングリコールなどのジ
オール化合物とから合成される繊維形成性ポリエステル
であり、構成単位の80モル%以上が、特に90モル%
以上がエチレンテレフタレート単位又はブチレンテレフ
タレート単位であるポリエステルが好ましい。また、ポ
リエステル中には、少量の添加剤、螢光増白剤、安定剤
あるいは、紫外線吸収剤などを含んでいても良い。The thermoplastic polyester resin referred to in the present invention is, for example,
Aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, naphthalene 2.6-dicarboxylic acid, phthalic acid, α, β-8 (4-carboxyphenoxy)ethane, 4.4°-dicarboxydiphenyl, 5-sodium sulfone isophthalic acid Acids or their esters and ethylene glycol, diethylene glycol,
■, 4°-butanediol, neopentyl glycol,
It is a fiber-forming polyester synthesized from diol compounds such as cyclohexane, 1,4'-dimetatool, polyethylene glycol, polytetramethylene glycol, etc., and 80 mol% or more of the constituent units are particularly 90 mol%.
Polyesters in which the above units are ethylene terephthalate units or butylene terephthalate units are preferred. The polyester may also contain small amounts of additives, fluorescent whitening agents, stabilizers, ultraviolet absorbers, and the like.
目的とする吸湿及び放湿性に優れた織編物を得る方法と
しては、特に、ポリエチレンテレフタレート、又は、ポ
リブチレンテレフタレートを主成分とするポリエステル
樹脂とケン化度95%以上にしてエチレン成分含量が3
0〜70モル%のエチレンビニルアルコールコポリマー
の2成分が、それぞれ、2成分ポリマーの集合状態が残
る程度に混合、または、複合させて繊維化することが重
量である。As a method for obtaining the desired woven or knitted fabric with excellent moisture absorption and moisture release properties, in particular, a polyester resin containing polyethylene terephthalate or polybutylene terephthalate as a main component and a saponification degree of 95% or more and an ethylene component content of 3.
The weight is that 0 to 70 mol% of the two components of the ethylene vinyl alcohol copolymer are mixed or composited to form fibers to such an extent that the aggregate state of the two component polymers remains.
吸湿性を有し、かつ繊維形成能を有する樹脂としては種
々のポリマーが知られているが、これらのポリマーのう
ちで特にエチレン酢酸ビニル共重合体ケン化物が吸湿時
のヤング率が高く、濡れた時にもベト付き感が少ない点
で優れている。Various polymers are known as resins that have hygroscopicity and fiber-forming ability, but among these polymers, saponified ethylene-vinyl acetate copolymer has a particularly high Young's modulus when absorbing moisture, and has a high wettability. It is excellent in that it does not feel sticky even when applied.
エチレンビニルアルコールコポリマー(以下、EVAL
と略記する場合がある)としては、ケン化度が95%以
上のケン化度物でエチレン成分が30〜70モル%のE
VALが最適である。EVAL中のエチレン成分含量が
高くなれば、当然に水酸基(OH)が減少するため、目
的とする親水性が得られなくなり、好ましくない。また
、エチレン成分含量が低くなりすぎると、溶融成型性が
低下するとともに、ポリエステルと紡糸直前に混合した
後、繊維化する際、曳糸性が不良となり、単糸切れ、断
糸が多くなり好ましくない。また、ポリエステルの紡糸
温度である250℃以上での耐熱性も不十分となること
からも適当でない。従って、高ケン化度EVALでエチ
レン成分含量が30〜70モル%のものが本目的の繊維
を得るためには適しているといえる。EVALの水酸基
はアルデヒド化合物によりアセタール化されていてもよ
く、より好ましくはジアルデヒド化合物、例えばグルタ
ルアルデヒドやグリオキザール等によりアセタール化さ
れている場合である。Ethylene vinyl alcohol copolymer (hereinafter referred to as EVAL)
) is a saponified product with a saponification degree of 95% or more and an ethylene component of 30 to 70 mol%.
VAL is optimal. If the content of the ethylene component in EVAL increases, the number of hydroxyl groups (OH) naturally decreases, making it impossible to obtain the desired hydrophilicity, which is not preferable. In addition, if the ethylene component content is too low, the melt formability will decrease, and when it is mixed with polyester immediately before spinning and then turned into fibers, the spinnability will be poor and single yarn breakage and yarn breakage will increase, so it is not preferable. do not have. Further, it is not suitable because the heat resistance at 250° C. or higher, which is the spinning temperature of polyester, is insufficient. Therefore, it can be said that EVAL with a high degree of saponification and an ethylene component content of 30 to 70 mol% is suitable for obtaining the fiber of the present purpose. The hydroxyl group of EVAL may be acetalized with an aldehyde compound, more preferably with a dialdehyde compound such as glutaraldehyde or glyoxal.
本発明において、EVALとポリエステルの重量比率を
5:95〜60:40の範囲で混合または複合させる必
要がある。E V A Lの重量比率が5重量%未満に
なると本発明のE V A Lのポリマー物性に基づく
親水性、特に、吸湿性の特性が顕在化しなくなり、好ま
しくない。また、60重量%以上になると、紡糸工程性
、延伸工程性が低下してくるため、好ましくないと共に
、繊維物性的にも本来のポリエステルの性能が低下し、
強度が低くなるため、好ましくない。また、用いるEV
ALの重合度があまり低くなると、紡糸時にポリエステ
ルとの溶融粘度差が大きくなり過ぎ、混合または複合ポ
リマーのバランスが悪くなり、紡糸性が低下し好ましく
ない。J I S −K −6730−1977に準拠
した190℃下2160gの荷重下でのメルトインデッ
クスが20以下であることが紡糸性から好ま1.い。In the present invention, it is necessary to mix or combine EVAL and polyester in a weight ratio of 5:95 to 60:40. If the weight ratio of EV A L is less than 5% by weight, the hydrophilic properties, especially the hygroscopic properties based on the polymer physical properties of the EV A L of the present invention will not become apparent, which is not preferable. Moreover, if it exceeds 60% by weight, the spinning process properties and the drawing process properties will deteriorate, which is not preferable, and the original performance of the polyester will decrease in terms of fiber properties.
This is not preferable because the strength becomes low. In addition, the EV used
If the degree of polymerization of AL is too low, the difference in melt viscosity from polyester during spinning becomes too large, the balance of the mixed or composite polymer deteriorates, and spinnability deteriorates, which is not preferable. From the viewpoint of spinnability, it is preferable that the melt index is 20 or less at 190° C. and under a load of 2160 g according to JIS-K-6730-1977. stomach.
さらに、本発明でいう混合とは、例えば(A)側ポリマ
ーと(B)側ポリマーをそれぞれ別々に溶融押出しし、
紡糸ノズルに至る前に、(A)対(B)の比率が所定の
重量比率となるように、スタチツクミキザーにより、あ
る程度均一あるいは不均一に混合させた後、紡糸ノズル
より押出すことにより、繊維化することである。また複
合とは、代表的には、(A)側ポリマーと(B)側ポリ
マーをそれぞれ別々に溶融押出しし、紡糸ノズルに至る
前に、(A)対(B)の比率が所定の重量比率となるよ
うに複合させた後、紡糸ノズルより押出すことにより、
繊維化することであり、例えば、繊維断面形態が芯鞘型
(第1図)やバイメタル型(第4図)、多層張り合せ型
(第5図)などがある。Furthermore, mixing in the present invention means, for example, melt-extruding the (A) side polymer and the (B) side polymer separately,
Before reaching the spinning nozzle, the ratio of (A) to (B) is mixed uniformly or non-uniformly to a certain extent using a static mixer so that the ratio is a predetermined weight ratio, and then extruded from the spinning nozzle. , to become fibrous. Composite typically means that the (A) side polymer and the (B) side polymer are melt-extruded separately, and the ratio of (A) to (B) is adjusted to a predetermined weight ratio before reaching the spinning nozzle. After compounding so that it becomes, by extruding it from a spinning nozzle,
For example, the cross-sectional shape of the fibers may be a core-sheath type (Fig. 1), a bimetal type (Fig. 4), or a multilayer laminated type (Fig. 5).
さらにまた、本発明は、かかる混合及びかかる複合を組
み合せて繊維化しても良く、例えば、芯鞘型繊維におい
て、芯成分に該(B)ポリマーを用い、鞘成分に該(A
)ポリマーと該(B)ポリマーの2成分を混合させたも
のを用いた複合繊維でも良い。Furthermore, in the present invention, such mixtures and composites may be combined to form fibers. For example, in a core-sheath type fiber, the (B) polymer is used as the core component and the (A) polymer is used as the sheath component.
) Polymer and the (B) polymer may be used as composite fibers made of a mixture of two components.
またさらに、本発明は、かかる混合または、複合繊維が
仮撚捲縮加工等の高次加工により、5角、6角に類似し
た繊維断面形状になったり、紡糸時の異形断面ノズルに
より、3葉形、T形、4葉形、5葉形、6葉形、7葉形
、8葉形等の多葉形や、各種の断面形状となっても本発
明の目的とする吸湿及び放湿にすぐれた織編物を得るこ
とができる。Furthermore, the present invention provides that the composite fiber can be formed into a fiber cross-sectional shape similar to pentagonal or hexagonal by high-order processing such as false twisting and crimping, or can be made into a three-sided fiber by using an irregular cross-sectional nozzle during spinning. Even if it has a multi-lobed shape such as leaf-shaped, T-shaped, four-lobed, five-lobed, six-lobed, seven-lobed, eight-lobed, etc., or various cross-sectional shapes, it can absorb and release moisture as the object of the present invention. It is possible to obtain excellent woven or knitted fabrics.
第1図〜7図は(A)側ポリマーと(B)側ポリマーか
ら成る複合繊維の例示であって、第1図は芯側か(B)
側ポリマー、鞘側が(A)側ポリマーあるいは、(A)
、 (B)混合ポリマーであるか、他の場合はどちらが
(A)側であっても良く、また真円である必要もなく楕
円や長方形や三角形、多角、形、多葉形であっても差し
つかえない。Figures 1 to 7 are examples of composite fibers consisting of a polymer on the (A) side and a polymer on the (B) side, and Figure 1 shows the core side (B).
side polymer, sheath side is (A) side polymer or (A)
, (B) is a mixed polymer, or in other cases, it does not matter which side is on the (A) side, and it does not need to be a perfect circle, but may be oval, rectangular, triangular, polygonal, shaped, or multilobed. I can't help it.
第8図は、本発明の織編物のもつ、放湿特性を説明する
線図てあり、かかる線図より本発明におけるY値が算出
される。FIG. 8 is a diagram illustrating the moisture release characteristics of the woven or knitted fabric of the present invention, and the Y value in the present invention is calculated from this diagram.
第9図は、本発明における織編物の吸水放散速度Yの測
定方法を説明する概略図である。FIG. 9 is a schematic diagram illustrating a method for measuring the water absorption/dissipation rate Y of a woven or knitted fabric according to the present invention.
以下、実施例により、本発明の織編物の具体的構成、効
果について説明するが、これによって本発明はなんら限
定されるものではない。Hereinafter, the specific structure and effects of the woven or knitted fabric of the present invention will be explained with reference to Examples, but the present invention is not limited thereto.
実施例1
エチレン含有量が48モル%のエチレンビニルアルコー
ルコポリマー(A)と固有粘度が0.70のポリエチレ
ンテレフタレート(B)を用いて、それぞれ別々の押出
し機にて溶融押出しし、(A)と(B)との複合比率が
30ニア0重量%となるよう複合させた後、その横断面
が第5図で示されるような多層複合繊維となるよう、紡
糸ノズルより、吐出m 3C1g/ m1ns紡糸巻き
取り速度1200m/minの条件で溶融紡糸した。得
られた紡糸原糸を通常のローラープレート方式の延伸機
を用いて、ホットローラー75℃、ホットプレート12
0℃、延伸倍率2.9倍の条件で延伸し、77d/24
fのマルチフィラメントを得た。単繊維の繊度は3.2
デニールであった。得られたマルチフィラメントを経糸
及び緯糸として使い厚さ0.7mm、目付160g/m
”のI/Iの平織物を製織した。製織工程も特に問題な
〈実施できた。かかる平織物をNN32C031/12
を含有する組成液の入った80℃の浴槽中で30分間糊
抜きした後、180℃で熱ト
セラし、その後約20%のアルカリ減量を実施した後、
以下の方法により染色した。Example 1 An ethylene vinyl alcohol copolymer (A) with an ethylene content of 48 mol% and a polyethylene terephthalate (B) with an intrinsic viscosity of 0.70 were melt-extruded using separate extruders to obtain (A) and After compounding so that the compounding ratio with (B) is 30 nia 0% by weight, the spinning nozzle discharges m3C1g/m1ns so that the cross section becomes a multilayer composite fiber as shown in Figure 5. Melt spinning was performed at a winding speed of 1200 m/min. The obtained spun yarn was heated with a hot roller at 75°C and a hot plate 12 using a normal roller plate type drawing machine.
Stretched at 0°C and a stretching ratio of 2.9 times, 77d/24
A multifilament of f was obtained. The fineness of single fiber is 3.2
It was denier. The obtained multifilament was used as the warp and weft with a thickness of 0.7 mm and a fabric weight of 160 g/m.
"I/I plain woven fabric was woven.The weaving process was also particularly problematic.
After de-sizing for 30 minutes in a bath at 80°C containing a composition solution containing the following, heat treatment was carried out at 180°C, and after that an alkali weight loss of about 20% was carried out.
It was stained by the following method.
文中に記載する方法に基づいて、測定、評価された。Measured and evaluated based on the method described in the text.
実施例2
実施例1と同一のエチレンビニルアルコールコポリマー
(A)とポリエチレンテレフタレート(B)を用いて、
それぞれ別々の押出し機にて溶融押出しし、(A)と(
B)の複合比率が50 : 50重量%となるよう複合
させた後、その横断面が第1図で示されるような芯鞘型
複合繊維となるよう、該複合ポリマーを紡糸ノズルより
、吐出量18g/min、紡糸巻き取り速度1000m
/minの条件で溶融紡糸した。得られた紡糸原糸を通
常のローラープレート方式の延伸機を用いて、ホットロ
ーラー75℃、ホットプレート125℃、延伸倍率3.
3倍の条件で延伸し、50d/24fのマルチフィラメ
ントを得た。単繊維の繊度は2デニールであった。得ら
れたマルチフィラメントを用いて厚さ0.18mm、目
付70g/m’の平織物[相])、厚さ1 、3mm、
目付200g/m’のフライス組織の編地(■)を作成
した。かかる織編物をアクチノールR−1001g/ρ
を含有した80℃の浴槽中で20分間糊抜きした後、グ
ルタルアルデヒド2g/ρ、硫酸8g/ρを含有する組
成液の入った浴槽に浸漬させ、90℃で50分間処理を
行い、その後、未架橋のアルデヒド基を消失させるため
、HtOa 5cc/12を含有する組成液にて80℃
、30分間処理した。次いで180℃で熱セットした後
、実施例1と同様の方法により染色し最後に170℃で
仕上げセットした。Example 2 Using the same ethylene vinyl alcohol copolymer (A) and polyethylene terephthalate (B) as in Example 1,
Melt extrusion was performed using separate extruders to obtain (A) and (
After compounding B) so that the compounding ratio is 50:50% by weight, the composite polymer is discharged from a spinning nozzle at a rate so that the cross section becomes a core-sheath type composite fiber as shown in FIG. 18g/min, spinning winding speed 1000m
Melt spinning was carried out under the conditions of /min. The obtained spun yarn was heated with a hot roller at 75°C, a hot plate at 125°C, and a stretching ratio of 3.
A multifilament of 50 d/24 f was obtained by stretching under 3 times the stretching conditions. The fineness of the single fiber was 2 denier. Using the obtained multifilament, a plain weave fabric with a thickness of 0.18 mm and a basis weight of 70 g/m' (phase), a thickness of 1 mm, 3 mm,
A milled knitted fabric (■) with a basis weight of 200 g/m' was prepared. Actinol R-1001g/ρ
After desizing for 20 minutes in a bath at 80°C containing In order to eliminate uncrosslinked aldehyde groups, the composition solution containing 5 cc/12 HtOa was heated at 80°C.
, and treated for 30 minutes. Then, after heat setting at 180°C, dyeing was carried out in the same manner as in Example 1, and finally finishing setting was carried out at 170°C.
得られた織編物は風合が非常に良好であり、本文中に記
載する方法に基づいて、測定、評価された。The obtained woven or knitted fabric had a very good feel, and was measured and evaluated based on the method described in the text.
実施例3
実施例1と同一のエチレンビニルアルコールコポリマー
とポリエチレンテレフタレートを用いて、その横断面が
第1図で示されるような芯鞘型複合繊維となるよう、芯
部には、かかるポリエチレンテレフタレートを用いて、
鞘部には、かかるエチレンビニルアルコールコポリマー
とかかるポリエチレンテレフタレートをスタチックミキ
サーにより混合比率15:85重量%となるよう混合さ
せ、かつ、かかる複合繊維の芯鞘複合比が1・2となる
よう該複合ポリマーを吐出量29g/min、紡糸巻き
取り速度800m/minの条件で溶融紡糸した。得ら
れた紡糸原糸を通常のローラープレート方式の延伸機を
用いて、ホットローラー75°C1ホツトプレート12
0℃、延伸倍率3.1倍の条件で延伸し、107d/3
6fのマルチフィラメントを得た。単繊維の繊度は3デ
ニールであった。得られたマルチフィラメントを用い、
厚さ0.9mm、目付130g/m”のマルチフィラメ
ントを用い、厚さ0 、9mn+、目付130g/m2
のフライス組織の編地を作成した。かかる編地をアクチ
ノールR−1001g/ρを含有した98°Cの浴槽中
で20分間糊抜きした後、180℃で熱セットし、その
後、130℃の高温水下で20分間処理した後、約20
%のアルカリ減量を実施した。その後の染色は、架橋剤
のNa2SO4及びH3BO3を除いた実施例1と同様
の方法により行なった。Example 3 Using the same ethylene vinyl alcohol copolymer and polyethylene terephthalate as in Example 1, such polyethylene terephthalate was added to the core so that the cross section became a core-sheath composite fiber as shown in FIG. make use of,
For the sheath portion, the ethylene vinyl alcohol copolymer and the polyethylene terephthalate are mixed in a static mixer at a mixing ratio of 15:85% by weight, and the composite fiber is mixed so that the core/sheath composite ratio is 1.2. The composite polymer was melt-spun under conditions of a discharge rate of 29 g/min and a spinning winding speed of 800 m/min. The obtained spun yarn was heated with a hot roller at 75°C1 using a normal roller plate type drawing machine.
Stretched at 0°C and a stretching ratio of 3.1 times, 107d/3
A 6f multifilament was obtained. The fineness of the single fiber was 3 denier. Using the obtained multifilament,
Using multifilament with a thickness of 0.9mm and a basis weight of 130g/m2, thickness 0, 9mm+, basis weight 130g/m2
A knitted fabric with a milling structure was created. The knitted fabric was desized in a 98°C bath containing Actinol R-1001g/ρ for 20 minutes, then heat set at 180°C, and then treated under high temperature water at 130°C for 20 minutes. 20
% alkali weight loss was carried out. The subsequent staining was carried out in the same manner as in Example 1 except that the crosslinking agents Na2SO4 and H3BO3 were excluded.
得られた編地は、風合が非常に良好であり、本文中に記
載する方法に基づいて測定評価された。The obtained knitted fabric had a very good feel, and was measured and evaluated based on the method described in the text.
比較例1
単繊維の繊度が2デニールである通常のポリエステルか
ら成る厚さ0.08mm、目付55g/m2の1/lの
平織物を本文中に記載する方法に基づいて測定、評価し
た。Comparative Example 1 A 1/l plain woven fabric with a thickness of 0.08 mm and a basis weight of 55 g/m 2 made of ordinary polyester with a single fiber fineness of 2 denier was measured and evaluated based on the method described in the text.
以上、実施例1〜3及び比較例1で示した織編物の、本
文中で記載する方法に準拠したX及びYの測定結果を第
1表及び第8図にまとめた。The results of measuring X and Y of the woven and knitted fabrics shown in Examples 1 to 3 and Comparative Example 1 according to the method described in the text are summarized in Table 1 and FIG. 8.
かかる第1表及び第8図かられかるように、実施例1,
2■)、3品は比較例2 ((Bl)、比較例1品に比
べて、吸湿率X及び織編物の吸水、放散速度Yにおいて
、優れた結果が得られており、本発明の特徴が現われて
いる。As can be seen from Table 1 and FIG. 8, Example 1,
2■) and 3 products obtained superior results in terms of moisture absorption rate X and water absorption and dissipation rate Y of woven and knitted fabrics compared to Comparative Example 2 ((Bl) and Comparative Example 1 product, which is a feature of the present invention. is appearing.
さらに、かかる実施例1〜3及び比較例1で示した織編
物を婦人用ブラウスに縫製し、パネラ−による人工気象
室での着用テストを行なった結果、実施例I、20)、
3品は、いづれも実施例2@)、比較例1品に比べて、
ムレ感やべとつき感が少なく快適であるという、パネラ
−の評価を得た。Furthermore, the woven and knitted fabrics shown in Examples 1 to 3 and Comparative Example 1 were sewn into women's blouses, and a panel wear test was conducted in an artificial climate chamber. As a result, Examples I, 20),
All three products were compared to Example 2@) and Comparative Example 1.
It was rated by panelists as being comfortable with little stuffiness or stickiness.
第
■
表
(発明の効果)
以上述へた通りの本発明によれば、ポリエステル繊維の
有する優れた汎用特性を生かして、かつ、吸湿及び放湿
性に優れた織編物が得られ、インチ中表、スポーツ衣料
等の用途に好適な、快適性にすぐれた衣料用素材が提供
されるものである。Table ■ (Effects of the Invention) According to the present invention as described above, it is possible to obtain a woven or knitted fabric that takes advantage of the excellent general-purpose properties of polyester fibers and has excellent moisture absorption and moisture release properties. The present invention provides a clothing material with excellent comfort and suitable for use in sports clothing and the like.
第1図〜7図は本発明を構成する代表的な多成分系繊維
の断面図である。第8図は、実施例および比較例で得ら
れた織編物のもつ・放湿特性を示す図であり、かかる図
より本発明におけるY値が算出される。第9図は、本発
明における織編物の吸水放散速度Yの測定方法を説明す
る概略図である。1 to 7 are cross-sectional views of typical multicomponent fibers constituting the present invention. FIG. 8 is a diagram showing the moisture release characteristics of the woven and knitted fabrics obtained in Examples and Comparative Examples, and the Y value in the present invention is calculated from this diagram. FIG. 9 is a schematic diagram illustrating a method for measuring the water absorption/dissipation rate Y of a woven or knitted fabric according to the present invention.
Claims (1)
共重合体のケン化ポリマー(A)と熱可塑性ポリエステ
ル系ポリマー(B)が重量比率(A):(B)=5:9
5〜60:40の範囲で合わされた単繊維繊度5デニー
ル以下の多成分系繊維からなる織編物であつて、該織編
物が次の吸湿率(X)および吸水放散速度(Y) X>1.5% Y>1.5%/分 を満足することを特徴とする織編物。[Claims] The saponified polymer (A) of an ethylene vinyl acetate copolymer having an ethylene content of 30 to 70 mol% and the thermoplastic polyester polymer (B) have a weight ratio (A):(B)=5: 9
A woven or knitted fabric consisting of multicomponent fibers with a single fiber fineness of 5 denier or less combined in a ratio of 5 to 60:40, the woven or knitted fabric having the following moisture absorption rate (X) and water absorption/diffusion rate (Y) X>1 A woven or knitted fabric characterized by satisfying .5% Y>1.5%/min.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007503A JP2849424B2 (en) | 1990-01-16 | 1990-01-16 | Woven and knitted fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007503A JP2849424B2 (en) | 1990-01-16 | 1990-01-16 | Woven and knitted fabric |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03213535A true JPH03213535A (en) | 1991-09-18 |
JP2849424B2 JP2849424B2 (en) | 1999-01-20 |
Family
ID=11667586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007503A Expired - Fee Related JP2849424B2 (en) | 1990-01-16 | 1990-01-16 | Woven and knitted fabric |
Country Status (1)
Country | Link |
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JP (1) | JP2849424B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06228820A (en) * | 1993-01-28 | 1994-08-16 | Kanebo Ltd | Durable water repellent and lightweight fiber structure |
WO2006008916A1 (en) * | 2004-07-02 | 2006-01-26 | Kuraray Co., Ltd. | Fabric and clothes for atopic dermatitis patients |
CN102534973A (en) * | 2012-01-31 | 2012-07-04 | 东华大学 | Colorful knitting fabric |
CN103397443A (en) * | 2013-07-26 | 2013-11-20 | 浙江鹏远新材料有限公司 | Halogen-free flame-retardant polyethylene plastic woven cloth and method for manufacturing same |
CN104195670A (en) * | 2014-08-16 | 2014-12-10 | 青岛供八方塑料有限公司 | Agricultural plastic woven fabric for greenhouses and preparation method thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS551372A (en) * | 1978-11-21 | 1980-01-08 | Gunze Kk | Fabric lettoff apparatus |
-
1990
- 1990-01-16 JP JP2007503A patent/JP2849424B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS551372A (en) * | 1978-11-21 | 1980-01-08 | Gunze Kk | Fabric lettoff apparatus |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06228820A (en) * | 1993-01-28 | 1994-08-16 | Kanebo Ltd | Durable water repellent and lightweight fiber structure |
WO2006008916A1 (en) * | 2004-07-02 | 2006-01-26 | Kuraray Co., Ltd. | Fabric and clothes for atopic dermatitis patients |
JPWO2006008916A1 (en) * | 2004-07-02 | 2008-05-01 | 株式会社クラレ | Fabrics and clothes for patients with atopic dermatitis |
CN102534973A (en) * | 2012-01-31 | 2012-07-04 | 东华大学 | Colorful knitting fabric |
CN103397443A (en) * | 2013-07-26 | 2013-11-20 | 浙江鹏远新材料有限公司 | Halogen-free flame-retardant polyethylene plastic woven cloth and method for manufacturing same |
CN104195670A (en) * | 2014-08-16 | 2014-12-10 | 青岛供八方塑料有限公司 | Agricultural plastic woven fabric for greenhouses and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2849424B2 (en) | 1999-01-20 |
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