JP2716695B2 - Blended yarn for clothing with humidity control function - Google Patents
Blended yarn for clothing with humidity control functionInfo
- Publication number
- JP2716695B2 JP2716695B2 JP61184666A JP18466686A JP2716695B2 JP 2716695 B2 JP2716695 B2 JP 2716695B2 JP 61184666 A JP61184666 A JP 61184666A JP 18466686 A JP18466686 A JP 18466686A JP 2716695 B2 JP2716695 B2 JP 2716695B2
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- hygroscopic
- denier
- moisture absorption
- fineness
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/207—Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
- D06M13/21—Halogenated carboxylic acids; Anhydrides, halides or salts thereof
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/02—Yarns or threads characterised by the material or by the materials from which they are made
- D02G3/04—Blended or other yarns or threads containing components made from different materials
- D02G3/045—Blended or other yarns or threads containing components made from different materials all components being made from artificial or synthetic material
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2401/00—Physical properties
- D10B2401/02—Moisture-responsive characteristics
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Mechanical Engineering (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Artificial Filaments (AREA)
- Drying Of Gases (AREA)
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、快適な衣料用繊維素材に関する。更に詳細
には調湿機能を有する衣料用素材の為の混紡糸に関す
る。
〔従来の技術及び問題点〕
合成繊維は多くの優れた特性を有するため広く利用さ
れるに到ったが、物が充足するにつれ快適な衣生活を求
める声が大きくなり、特に直接肌に接して用いられる基
礎衣料品の多くは天然繊維が用いられている。これは合
成繊維が吸水性、吸湿性の面で著しく劣るのも大きな原
因と考えられる。
従来より合成繊維に吸水性、吸湿性を付与するため数
多くの方法が提案されている(特開昭54−93121号公
報、特開昭60−155770号公報等)が、いずれも天然繊維
の特質を越えることが出来ない。特に吸湿性において天
然繊維以上の容量を有する改良は繊維としての諸物性が
著しく低下してしまうため実用化されていない。
又、天然繊維を見ると調湿機能から見て絹が最も優れ
ているが、取り扱いのし難さ、経済性等からみて極く限
られた範囲でしか実用化されておらず、主として綿が用
いられている。
〔発明の目的〕
本発明者は衣服内湿度の変化を追求した結果、吸湿性
の大きな繊維を出来るだけ絶乾に近い状態まで乾燥し着
用に供した場合、衣服内湿度の上昇が遅く、着用者はム
レ感の少ない時間を長く感じることができることを見出
した。一方、改質により吸湿量を増大させた繊維を用い
た場合は、繊維物性が著しく低下し実用にはそぐわない
ことが観察された。
そこで、これらの欠点を改善し、吸湿性の良さを生か
す方法について鋭意研究を続けた結果、まず吸湿性の強
いカルボキシメチル化レーヨン、ポリビニルアルコール
繊維を調べると吸水により収縮したり、乾燥後硬くなっ
たり、強度が著しく低下したりし、この欠点を補うため
非吸湿性繊維であるポリエステル、ポリプロピレン、ポ
リ塩化ビニルと混紡又は混繊した場合、非吸湿性繊維を
その比率が50重量%以上、好ましくは55〜65重量%とな
るような割合で混合することにより大きく改善され調湿
機能が保持される事を見出した。
当然のことではあるが、吸湿性改善の限度は繊維が水
に溶解しないことであり、繊維改質時の置換度、ベース
となる繊維の重合度が大きく影響する。溶解性をコント
ロールするため架橋等により調整の手段を講ずることも
可能である。
このようにして繊維物性から単独では実用にならない
カルボキシメチル化レーヨン、ポリビニルアルコール繊
維等の繊維を混紡することにより公知の工程を経て編織
物となし衣料用としたときムレを感じさせない快適な衣
料が得られることを見出した。
本発明はかかる知見に基づいて更に見当を重ね研究し
た結果完成したものである。
〔発明の構成〕
即ち、本発明は、少なくとも2種以上の繊維からなる
混紡糸において、ポリエステル、ポリプロピレン、ポリ
塩化ビニルから選ばれる1種もしくは2種以上の非吸湿
性繊維を50〜80重量%、及びカルボキシメチル化レーヨ
ン又はポリビニルアルコール繊維から選ばれる吸湿性繊
維を20〜50重量%含有し、温度20℃環境相対湿度65%に
おける平衡吸湿率が絶乾重量に対して15%以下であり、
温度29.5℃環境相対湿度96%における平衡吸湿率が絶乾
重量に対して35%以上であることを特徴とする調湿機能
を有する衣料用混紡糸に係わるものである。
本発明における混紡糸とはフィラメント繊維とステー
プル繊維より構成される糸を含む。
本発明に用いられる吸湿性繊維としては、温度29.5℃
環境相対湿度96%における平衡吸湿率が絶乾重量に対し
て70%以上であるものが好ましく、具体的には、カルボ
キシメチル化レーヨン、ポリビニルアルコール繊維等が
挙げられる。
セルロース系繊維はセルロースの重合度により、その
好ましいカルボキシメチル化の程度が異なり、例えばビ
スコースレーヨンの場合は0.15〜0.18程度が最も良い。
ポリノジックレーヨンのように分子量の大きな場合は0.
19〜0.22程度が最も良い。これ以上の置換度の場合は溶
解し易くなる。後架橋により溶解を抑えることも可能で
あり、最も簡単な方法としてアルミニウムイオンを用い
ることができる。しかし何れの方法によって得られたカ
ルボキシメチル化レーヨン繊維も単独では水に濡らして
乾燥した場合に、繊維をのりずけした如く硬くなり、ま
た引張強度も低下し、更に悪いことには、繊維の収縮が
起こり衣料品としたときの寸法安定性に欠けるなどの欠
点を有する。
他の例についても同様であり、ポリビニルアルコール
繊維の場合、平均重合度により鹸化の程度が異なるが、
所望の吸湿量を出すには、鹸化度98モル%以上がよい。
この繊維も単独ではカルボキシメチル化レーヨン繊維と
同様硬く強度低下もある。
本発明で用いられる非吸湿性繊維としては、温度20℃
環境相対湿度65%における平衡吸湿率が絶乾重量に対し
て5%以下であるものが好ましく、具体的には、一般に
市販されているポリエステル、ポリプロピレン、ポリ塩
化ビニルが挙げられ、又これらの表面に物理的変化を加
えたものや、化学的に改質を加えたもの、即ち微細な綿
状溝もしくは微細孔を有する繊維でもよい。吸湿性等の
改質を施したものは一般に強度が低く且つ吸湿性繊維と
の親和性が高いため吸水吸湿後の乾燥により硬くなる欠
点が有る。
本発明において、非吸湿性繊維の強度は吸湿性繊維の
脆さを補うため一定の大きさが必要であり、引張強度で
見ると乾燥状態でデニール当たり5.0g/D以上がよい。
又、繊度は肌に接して用いる為、出来るだけ細い方がよ
く3デニール以下が良い。好ましくは、0.8〜1.5デニー
ルがよい。
本発明の混紡糸は、非吸湿性繊維50〜80重量%、及び
吸湿性繊維20〜50重量%を含有し、温度20℃環境相対湿
度65%における平衡吸湿率が絶乾重量に対して15%以下
であり、温度29.5℃環境相対湿度96%における平衡吸湿
率が絶乾重量に対して35%以上である。特に非吸湿性繊
維の含有比率が55〜65重量%のものが好ましい。吸湿性
繊維と非吸湿性繊維の混綿は通常の方法で実施出来る。
繊維の繊度は出来るだけ細くし、糸は細い番手とし、撚
り数を多くすることにより強度を高めるとよい。更に非
吸湿性繊維を糸断面で見て外側に来るよう芯鞘構造の紡
績糸とすればなお望ましい。吸湿性繊維が長繊維である
場合は、公知の方法により非吸湿性繊維を鞘状に巻きつ
けた芯鞘構造が特に望ましい(特開昭52−59745号公報
参照)。
目的の糸を作る方法には、吸湿性繊維と非吸湿性繊維
を予め準備しておいて公知の方法により紡績する方法
と、予め混率を決めた吸湿性繊維ベース繊維と非吸湿性
繊維の混紡糸をチーズコーンに巻き吸湿性繊維に改質す
る方法がある。何れの方法を採用するかはケースバイケ
ースであるが、吸湿性を高めた場合には繊維物性面から
見て従来の装置を通過させにくくなるため、吸湿性ベー
ス繊維を所定量混綿し紡績糸又は混繊糸としたあと改質
反応により所望の物を得るとよい。
尚、本発明による混紡糸は、繊維の硬さ、及び表面物
性の変化のため以後の工程中における摩擦が大きくな
る。この欠点は工程油剤を選ぶことにより解決できる。
以上の方法により得られた混紡糸を用いて、例えば靴
下、肌着等の衣料品を作ると、特にムレ感のすくない快
適な製品が得られる。
〔発明の効果〕
以上説明したように、本発明の混紡糸はその構成成分
中に低い相対湿度条件下(例えば温度20℃相対湿度65
%)での吸湿量が少なく、比較的高い相対湿度条件下
(例えば温度29.5℃相対湿度96%)での吸湿量が多い成
分を含むため、人体表面の温度及び湿度上昇に伴い吸湿
機能を発揮し、衣服内環境の湿度上昇を緩和させる働き
を有し、更には外界の気流及び温度低下に伴う蒸気圧の
低下により放湿をし衣服内環境の温湿度変化を緩和する
ことができる。この働きのため、本発明の混紡糸を用い
て、官能的にはムレ感の少ない暑熱感の少ない肌着等の
基礎衣料を得ることができる。更には洗濯後の乾燥、衣
服保管時の環境変化においても通常の状態では、放湿も
よく、吸湿による保管中の不都合も起こり難い。
〔実施例〕
以下に実施例を挙げて本発明を更に詳細に説明する
が、本発明はこれらの実施例に限定されるものではな
い。
尚、実施中の%は重量%を示す。
実施例1
ポリエステル繊維
繊度2 デニール 80%
ビスコースレーヨン
繊度1.5デニール 20%
の混紡糸に、セルロース1モルに対して、目的とするカ
ルボキシメチル化度の3倍のモル数のモノクロル酢酸、
その2.2倍の水酸化ナトリウムを加えて、室温で30分間
マーセル化、続いて60℃で120分間カルボキシメチル化
を行い、過剰の水酸化ナトリウムを酢酸にて中和、水洗
し、油剤処理を行った後、60分間熱風乾燥を行って改質
糸を得た。カルボキシメチル化度は0.2であった。反応
後の繊維組成比は表1に示す如く変動した。
実施例2
ポリエステル繊維
繊度2 デニール 65%
ビスコースレーヨン
繊度1.5デニール 35%
の混紡糸を実施例1と同様の方法に従ってカルボキシメ
チル化した。カルボキシメチル化度は0.13であった。反
応後の繊維組成比は表1に示す如く変動した。
実施例3
ポリ塩化ビニール繊維
繊度2 デニール 65%
ビスコースレーヨン
繊度1.5デニール 35%
の混紡糸を実施例1と同様の方法に従ってカルボキシメ
チル化した。カルボキシメチル化度は0.13であった。
実施例4
ポリエステル繊維
繊度2 デニール 55%
ビスコースレーヨン
繊度1.5デニール 45%
の混紡糸を実施例1と同様の方法に従ってカルボキシメ
チル化した。カルボキシメチル化度は0.09であった。反
応後の繊維組成比は表1に示す如く変動した。
比較例1
ポリエステル繊維
繊度2 デニール 50%
ビスコースレーヨン
繊度1.5デニール 50%
の混紡糸を実施例1と同様の方法に従ってカルボキシメ
チル化した。カルボキシメチル化度は0.09であった。反
応後の繊維組成比は表1に示す如く変動した。
比較例2
ポリエステル繊維
繊度2 デニール 65%
ビスコースレーヨン
繊度1.5デニール 35%
の混紡糸である。
実施例5
ポリビニルアルコール繊維
(重合度1700、鹸化度99.0%)
繊度2 デニール 20%
ポリエステル繊維
繊度2 デニール 80%
上記2種の繊維を混綿し紡績糸とした。
実施例6
ポリビニルアルコール繊維
(重合度1700、鹸化度99.9%)
繊度1.5デニール 35%
ポリエステル繊維
繊度2 デニール 65%
上記2種の繊維を混綿し紡績糸とした。
実施例7
ポリビニルアルコール繊維
(重合度2000、鹸化度99.9%)
繊度2 デニール 45%
ポリエステル繊維
繊度2 デニール 55%
上記2種の繊維を混綿し紡績糸とした。
実施例8
ポリビニルアルコール繊維
(重合度1700、鹸化度99.9%)
繊度1.5デニール 30%
ポリプロピレン繊維
繊度2 デニール 70%
上記2種の繊維を混綿し紡績糸とした。
比較例3
ポリビニルアルコール繊維
(重合度2000、鹸化度99.9%)
繊度2 デニール 55%
ポリエステル繊維
繊度2 デニール 45%
上記2種の繊維を混綿し紡績糸とした。
比較例4
ポリビニルアルコール繊維
(重合度1700、鹸化度99.0%)
繊度2 デニール 15%
ポリエステル繊維
繊度2 デニール 85%
上記2種の繊維を混綿し紡績糸とした。
実施例1〜8及び比例例1〜4で得られた糸の強度、
吸湿率、吸湿性繊維の吸湿率及び乾燥時の硬さを評価
し、表1に示した。
又、参考例として、綿、羊毛、絹の評価結果も表1に
示した。
尚、吸湿率は試料の乾燥重量と所定の温度及び相対湿
度における重量とから、次の式により求めた。
吸湿率A;温度20℃相対湿度65%における平衡吸湿率。
吸湿率B;温度29.5℃相対湿度96%における平衡吸湿率実施例9
ポリエステル繊維
繊度2 デニール 65%
ビスコースレーヨン
繊度1.5デニール 35%
を実施例1と同様の方法に従ってカルボキシメチル化
し、カルボキシメチル化度0.14の40S混紡糸を得た。
これを2本引き揃えて、東レ・デュポン社製のオペロ
ン繊維20%と共に靴下を編成した。
又、比較例として、
綿40S 2本引き揃え 80%
オペロン 20%
で同様に靴下を編成した。
6月中旬より7月中旬にかけ、1ケ月間、男子パネラ
ー30名により着用テストを実施した。その結果を以下に
示す。 The present invention relates to a comfortable textile material for clothing. More particularly, it relates to a blend yarn for a clothing material having a humidity control function. [Conventional technology and problems] Synthetic fibers have come to be widely used because of their many excellent properties. Most of the basic clothing used is made of natural fibers. This is probably because synthetic fibers are remarkably inferior in water absorption and hygroscopicity. Many methods have conventionally been proposed for imparting water absorbency and hygroscopicity to synthetic fibers (JP-A-54-93121, JP-A-60-155770, etc.). Cannot be exceeded. In particular, an improvement having a capacity higher than that of the natural fiber in the hygroscopic property has not been put to practical use because the physical properties of the fiber are significantly reduced. In terms of the natural fiber, silk is the best in terms of the humidity control function, but it is only practically used in a very limited range in view of the difficulty in handling and economics. Used. [Object of the Invention] As a result of pursuing changes in humidity in clothes, the present inventor has found that, when fibers having large hygroscopicity are dried to a state as close to absolutely dry as possible and provided for wearing, the rise in humidity in clothes is slow, and Found that they can feel the time with less stuffiness longer. On the other hand, it was observed that when the fiber whose moisture absorption was increased by the modification was used, the physical properties of the fiber were remarkably reduced, which was not suitable for practical use. Therefore, as a result of intensive research on ways to improve these disadvantages and take advantage of the good hygroscopicity, firstly, when examining carboxymethylated rayon and polyvinyl alcohol fiber with strong hygroscopicity, they shrink due to water absorption and become hard after drying. Or, the strength is remarkably reduced, and in order to compensate for this drawback, when blended or blended with non-hygroscopic fibers such as polyester, polypropylene, and polyvinyl chloride, the ratio of the non-hygroscopic fibers is 50% by weight or more, preferably Was found to be greatly improved by mixing at a ratio of 55 to 65% by weight to maintain the humidity control function. As a matter of course, the limit of improvement in hygroscopicity is that the fiber is not dissolved in water, and the degree of substitution during fiber modification and the degree of polymerization of the base fiber are greatly affected. In order to control the solubility, it is also possible to take measures for adjustment by crosslinking or the like. In this way, carboxymethylated rayon, which is not practically used alone from the fiber physical properties, by knitting fibers such as polyvinyl alcohol fibers, etc., through a known process, a knitted fabric and a comfortable garment that does not feel stuffy when used for clothing. It was found that it could be obtained. The present invention has been completed as a result of further research based on such findings. [Constitution of the Invention] That is, the present invention relates to a blended yarn comprising at least two or more fibers, wherein one or two or more non-hygroscopic fibers selected from polyester, polypropylene and polyvinyl chloride are contained in an amount of 50 to 80% by weight. And 20 to 50% by weight of a hygroscopic fiber selected from carboxymethylated rayon or polyvinyl alcohol fiber, and the equilibrium moisture absorption at a temperature of 20 ° C and an environmental relative humidity of 65% is 15% or less based on the absolute dry weight,
The present invention relates to a blended yarn for clothing having a humidity control function, wherein the equilibrium moisture absorption at a temperature of 29.5 ° C. and an environmental relative humidity of 96% is 35% or more based on the absolute dry weight. The blended yarn in the present invention includes a yarn composed of a filament fiber and a staple fiber. The hygroscopic fiber used in the present invention has a temperature of 29.5 ° C.
It is preferable that the equilibrium moisture absorption at an environmental relative humidity of 96% is 70% or more based on the absolute dry weight, and specific examples thereof include carboxymethylated rayon and polyvinyl alcohol fiber. The preferable degree of carboxymethylation of the cellulosic fiber varies depending on the degree of polymerization of the cellulose. For example, in the case of viscose rayon, about 0.15 to 0.18 is the best.
0 if the molecular weight is large, such as polynosic rayon.
About 19-0.22 is best. If the degree of substitution is higher than this, it becomes easy to dissolve. Dissolution can be suppressed by post-crosslinking, and aluminum ions can be used as the simplest method. However, when the carboxymethylated rayon fiber obtained by any of the methods alone is wetted with water and dried, the fiber becomes hard as if the fiber has been peeled off, and the tensile strength is reduced. It has drawbacks such as shrinkage and lack of dimensional stability when made into clothing. The same applies to other examples, and in the case of polyvinyl alcohol fiber, the degree of saponification varies depending on the average degree of polymerization,
In order to obtain a desired moisture absorption, the saponification degree is preferably 98 mol% or more.
This fiber alone is hard and has a reduced strength similarly to the carboxymethylated rayon fiber. The non-hygroscopic fiber used in the present invention has a temperature of 20 ° C.
It is preferable that the equilibrium moisture absorption at an environmental relative humidity of 65% is 5% or less based on the absolute dry weight, and specifically, commercially available polyester, polypropylene and polyvinyl chloride are mentioned. The fibers may be those obtained by physically changing or chemically modified, that is, fibers having fine flocculent grooves or fine pores. Those having been modified in terms of hygroscopicity generally have low strength and high affinity with hygroscopic fibers, and thus have a drawback that they become harder by drying after absorbing water. In the present invention, the strength of the non-hygroscopic fiber needs to have a certain size in order to compensate for the brittleness of the hygroscopic fiber. In terms of tensile strength, it is preferably at least 5.0 g / D per denier in a dry state.
The fineness should be as thin as possible and 3 denier or less, because it is used in contact with the skin. Preferably, 0.8 to 1.5 denier is good. The blended yarn of the present invention contains 50 to 80% by weight of a non-hygroscopic fiber and 20 to 50% by weight of a hygroscopic fiber, and has an equilibrium moisture absorption at a temperature of 20 ° C. and an environmental relative humidity of 65% relative to the absolute dry weight. %, And the equilibrium moisture absorption at a temperature of 29.5 ° C and an environmental relative humidity of 96% is 35% or more based on the absolute dry weight. In particular, those having a non-hygroscopic fiber content ratio of 55 to 65% by weight are preferred. The cotton blending of the hygroscopic fiber and the non-hygroscopic fiber can be carried out by a usual method.
The fineness of the fiber should be as small as possible, the yarn should be fine, and the strength should be increased by increasing the number of twists. Further, it is more desirable that the non-hygroscopic fiber is a spun yarn having a core-sheath structure so that the non-hygroscopic fiber comes to the outside as viewed in the yarn cross section. When the hygroscopic fiber is a long fiber, a core-sheath structure in which a non-hygroscopic fiber is wound in a sheath shape by a known method is particularly desirable (see JP-A-52-59745). The method for producing the target yarn includes a method in which a hygroscopic fiber and a non-hygroscopic fiber are prepared in advance and spinning is performed by a known method, and a method in which a hygroscopic fiber base fiber and a non-hygroscopic fiber having a predetermined blending ratio are mixed. There is a method in which a yarn is wound around a cheese cone and modified into a hygroscopic fiber. Which method is adopted is case-by-case, but when the moisture absorption is increased, it becomes difficult to pass through the conventional device from the viewpoint of fiber physical properties. Alternatively, a desired product may be obtained by a modification reaction after forming a mixed fiber. In the blended yarn according to the present invention, the friction during the subsequent steps increases due to the change in the hardness and surface physical properties of the fiber. This disadvantage can be solved by selecting a process oil. When a garment such as a sock or an undergarment is made using the blended yarn obtained by the above method, a comfortable product with less stuffiness can be obtained. [Effects of the Invention] As described above, the blended yarn of the present invention has a low relative humidity condition (for example, a temperature of 20 ° C and a relative humidity of 65%) in its constituent components.
%) And contains a large amount of moisture under relatively high relative humidity conditions (for example, temperature of 29.5 ° C and relative humidity of 96%). In addition, it has a function of alleviating a rise in the humidity of the environment inside the clothes, and further, it can release moisture due to a decrease in the vapor pressure due to the airflow in the outside world and a decrease in the temperature, thereby mitigating changes in the temperature and humidity of the environment inside the clothes. Due to this function, it is possible to obtain a basic garment such as underwear with less sensation of heat and less hot feeling by using the blended yarn of the present invention. In addition, in a normal state, even after drying after washing and changes in the environment during storage of clothes, moisture is well released, and inconvenience during storage due to moisture absorption hardly occurs. [Examples] Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to these Examples. The percentages during the execution indicate weight percentages. Example 1 Polyester fiber Fineness 2 denier 80% Viscose rayon Monodenic acetic acid having a mole number of 3 times the intended carboxymethylation degree per 1 mole of cellulose was mixed with a blended yarn having a fineness of 1.5 denier 20%.
Add 2.2 times that amount of sodium hydroxide, perform mercerization at room temperature for 30 minutes, then perform carboxymethylation at 60 ° C for 120 minutes, neutralize excess sodium hydroxide with acetic acid, wash with water, and perform oil treatment. After that, hot air drying was performed for 60 minutes to obtain a modified yarn. The degree of carboxymethylation was 0.2. The fiber composition ratio after the reaction varied as shown in Table 1. Example 2 Polyester Fiber Fineness 2 Denier 65% Viscose Rayon A blended yarn having a fineness of 1.5 denier 35% was carboxymethylated in the same manner as in Example 1. The degree of carboxymethylation was 0.13. The fiber composition ratio after the reaction varied as shown in Table 1. Example 3 Polyvinyl chloride fiber Fineness 2 denier 65% Viscose rayon A blend yarn having a fineness 1.5 denier 35% was carboxymethylated in the same manner as in Example 1. The degree of carboxymethylation was 0.13. Example 4 Polyester Fiber Fineness 2 Denier 55% Viscose Rayon A blended yarn having a fineness 1.5 denier 45% was carboxymethylated in the same manner as in Example 1. The degree of carboxymethylation was 0.09. The fiber composition ratio after the reaction varied as shown in Table 1. Comparative Example 1 Polyester Fiber Fineness 2 Denier 50% Viscose Rayon A blended yarn having a fineness 1.5 denier 50% was carboxymethylated in the same manner as in Example 1. The degree of carboxymethylation was 0.09. The fiber composition ratio after the reaction varied as shown in Table 1. Comparative Example 2 Polyester Fiber Fineness 2 Denier 65% Viscose Rayon A blended yarn with a fineness of 1.5 denier 35%. Example 5 Polyvinyl alcohol fiber (degree of polymerization: 1700, degree of saponification: 99.0%) Fineness: 2 denier 20% Polyester fiber Fineness: 2 denier 80% The above two types of fibers were mixed to form a spun yarn. Example 6 Polyvinyl alcohol fiber (degree of polymerization: 1700, degree of saponification: 99.9%) Fineness: 1.5 denier 35% Polyester fiber: fineness: 2 denier 65% The above two kinds of fibers were mixed to form a spun yarn. Example 7 Polyvinyl alcohol fiber (degree of polymerization: 2,000, degree of saponification: 99.9%) Fineness: 2 denier 45% Polyester fiber: fineness: 2 denier 55% The above two types of fibers were mixed to form a spun yarn. Example 8 Polyvinyl alcohol fiber (degree of polymerization: 1700, degree of saponification: 99.9%) Fineness: 1.5 denier 30% Polypropylene fiber: fineness: 2 denier 70% The above two kinds of fibers were mixed to form a spun yarn. Comparative Example 3 Polyvinyl alcohol fiber (degree of polymerization: 2,000, degree of saponification: 99.9%) Fineness: 2 denier 55% Polyester fiber Fineness: 2 denier 45% The above two types of fibers were mixed to form a spun yarn. Comparative Example 4 Polyvinyl alcohol fiber (degree of polymerization: 1700, degree of saponification: 99.0%) Fineness: 2 denier 15% Polyester fiber: fineness: 2 denier 85% The above two kinds of fibers were mixed to form a spun yarn. Strength of the yarn obtained in Examples 1 to 8 and proportional examples 1 to 4,
The moisture absorption, the moisture absorption of the hygroscopic fiber, and the hardness during drying were evaluated, and the results are shown in Table 1. Table 1 also shows the evaluation results of cotton, wool, and silk as reference examples. The moisture absorption was determined by the following equation from the dry weight of the sample and the weight at a predetermined temperature and relative humidity. Moisture absorption A; Equilibrium moisture absorption at a temperature of 20 ° C and a relative humidity of 65%. Moisture absorption B; Equilibrium moisture absorption at 29.5 ° C and 96% relative humidity Example 9 Polyester fiber Fineness 2 denier 65% Viscose rayon 1.5 denier 35% fineness was carboxymethylated in the same manner as in Example 1 to obtain a 40S blended yarn having a carboxymethylation degree of 0.14. Two of these were aligned and a sock was knitted with 20% operon fiber manufactured by Dupont Toray. As a comparative example, socks were similarly knitted with two 40S cotton 80% operons. From mid-June to mid-July, 30 male panelists conducted a wearing test for one month. The results are shown below.
Claims (1)
て、ポリエステル、ポリプロピレン、ポリ塩化ビニルか
ら選ばれる1種もしくは2種以上の非吸湿性繊維を50〜
80重量%、及びカルボキシメチル化レーヨン又はポリビ
ニルアルコール繊維から選ばれる吸湿性繊維を20〜50重
量%含有し、温度20℃環境相対湿度65%における平衡吸
湿率が絶乾重量に対して15%以下であり、温度29.5℃環
境相対湿度96%における平衡吸湿率が絶乾重量に対して
35%以上であることを特徴とする調湿機能を有する衣料
用混紡糸。 2.非吸湿性繊維の温度20℃環境相対湿度65%における
平衡吸湿率が絶乾重量に対して5%以下であり、吸湿性
繊維の温度29.5℃環境相対湿度96%における平衡吸湿率
が絶乾重量に対して70%以上である特許請求の範囲第1
項記載の混紡糸。(57) [Claims] In a blended yarn comprising at least two or more fibers, one or two or more non-hygroscopic fibers selected from polyester, polypropylene and polyvinyl chloride are mixed with 50 to 50%.
80% by weight, and 20 to 50% by weight of hygroscopic fiber selected from carboxymethylated rayon or polyvinyl alcohol fiber. Equilibrium moisture absorption at a temperature of 20 ° C and a relative humidity of 65% is 15% or less based on the absolute dry weight. The equilibrium moisture absorption at a temperature of 29.5 ° C and a relative humidity of 96% is based on the absolute dry weight.
A blend yarn for clothing having a humidity control function of 35% or more. 2. The equilibrium moisture absorption of the non-hygroscopic fiber at a temperature of 20 ° C and an environmental relative humidity of 65% is 5% or less of the absolute dry weight, and the equilibrium moisture absorption of the hygroscopic fiber at a temperature of 29.5 ° C and an environmental relative humidity of 96% is an absolute dry weight. Claim 1 which is 70% or more with respect to
The blended yarn according to the above item.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61184666A JP2716695B2 (en) | 1986-08-06 | 1986-08-06 | Blended yarn for clothing with humidity control function |
EP87111036A EP0255697A3 (en) | 1986-08-06 | 1987-07-30 | Blended yarn having moisture conditioning |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61184666A JP2716695B2 (en) | 1986-08-06 | 1986-08-06 | Blended yarn for clothing with humidity control function |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6342929A JPS6342929A (en) | 1988-02-24 |
JP2716695B2 true JP2716695B2 (en) | 1998-02-18 |
Family
ID=16157231
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61184666A Expired - Lifetime JP2716695B2 (en) | 1986-08-06 | 1986-08-06 | Blended yarn for clothing with humidity control function |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0255697A3 (en) |
JP (1) | JP2716695B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011034257A1 (en) * | 2009-09-17 | 2011-03-24 | Hwang Duck Yeul | Method for manufacturing hair-blended yarn consisting of polyester stable fiber and viscose rayon stable fiber |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX9709322A (en) * | 1995-06-07 | 1998-02-28 | Allied Signal Inc | Carpet and yarns therefor. |
JP3260268B2 (en) * | 1995-12-18 | 2002-02-25 | 宇部興産株式会社 | Polypropylene resin composition |
JP4514865B2 (en) * | 1999-12-22 | 2010-07-28 | 旭化成せんい株式会社 | Wetting substrate and method of using the same |
CN114645352A (en) * | 2020-12-21 | 2022-06-21 | 上海纺织(集团)大丰纺织有限公司 | Viscose fiber and diacetate fiber blended yarn and manufacturing process thereof |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB767889A (en) * | 1954-03-05 | 1957-02-06 | Bemberg Ag | A method for the production of yarn or thread |
JPS589174B2 (en) * | 1975-11-14 | 1983-02-19 | 帝人株式会社 | Goseisen Ioriamimono |
JPS5520006A (en) * | 1978-07-28 | 1980-02-13 | Marukou Kogyo Kk | Noise filter circuit |
-
1986
- 1986-08-06 JP JP61184666A patent/JP2716695B2/en not_active Expired - Lifetime
-
1987
- 1987-07-30 EP EP87111036A patent/EP0255697A3/en not_active Withdrawn
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011034257A1 (en) * | 2009-09-17 | 2011-03-24 | Hwang Duck Yeul | Method for manufacturing hair-blended yarn consisting of polyester stable fiber and viscose rayon stable fiber |
Also Published As
Publication number | Publication date |
---|---|
JPS6342929A (en) | 1988-02-24 |
EP0255697A2 (en) | 1988-02-10 |
EP0255697A3 (en) | 1990-04-04 |
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