JPH0359130A - Polyester blended yarn having different shrinkage - Google Patents
Polyester blended yarn having different shrinkageInfo
- Publication number
- JPH0359130A JPH0359130A JP1190279A JP19027989A JPH0359130A JP H0359130 A JPH0359130 A JP H0359130A JP 1190279 A JP1190279 A JP 1190279A JP 19027989 A JP19027989 A JP 19027989A JP H0359130 A JPH0359130 A JP H0359130A
- Authority
- JP
- Japan
- Prior art keywords
- shrinkage
- yarn
- fiber
- polyester
- less
- 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
Landscapes
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Artificial Filaments (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野1
本発明は透けを防止し、ミルキーな光沢、ふくらみ、ド
レープ性、ソフト感に富み、特に従来技術では創出しえ
なかった、繊細なドライタッチ風合を有する薄地織編物
を構成する糸条として好適であるポリエステル収縮差混
繊糸に関する。[Detailed Description of the Invention] [Industrial Application Field 1] The present invention prevents see-through, has a milky luster, fullness, drapability, and a soft feel, and especially has a delicate dry touch that could not be created with conventional technology. The present invention relates to a polyester shrinkage blend yarn suitable as a yarn constituting a thin woven or knitted fabric having a texture.
[従来の技術]
現在、ポリエステル繊維はこのN維が持つイージーケア
性などから衣料用途に広く用いられている。この衣料1
1途の中で、特に薄地衣料の分野においては光の透過性
の制御、いわゆる透けの防止が不可欠である。この目的
のために、光遮蔽剤として酸化チタン等の艶消し剤を含
有させたポリエステル繊維が薄地衣料用として広く用い
られて成功をおさめている。また酸化チタン等の粒子は
、単に繊維中の光遮蔽剤とじて動くのみではなく最終製
品である織編物から合成繊維特有のヌメリ感をなくし、
サランとしたドライタッチな風合やミルキーな光沢を付
与する効果を持っている。これは繊維中の艶消し剤が光
を乱反射するとともに、織編物を製造する際に通常行わ
れるアルカリ減量処理によりm維表面近辺の艶消し剤が
脱落し繊維の表面にm細な凹凸が発現するためであると
考えられている。[Prior Art] Currently, polyester fibers are widely used in clothing applications due to the easy care properties of N fibers. This clothing 1
Particularly in the field of thin clothing, it is essential to control light transmittance, that is, to prevent so-called see-through. For this purpose, polyester fibers containing matting agents such as titanium oxide as light shielding agents have been widely used successfully for thin clothing. In addition, particles such as titanium oxide not only move with the light shielding agent in the fibers, but also eliminate the sliminess characteristic of synthetic fibers from the final woven or knitted fabric.
It has the effect of imparting a saran dry touch texture and a milky luster. This is because the matting agent in the fibers diffusely reflects light, and the matting agent near the surface of the fibers falls off due to the alkali weight loss treatment that is normally performed when manufacturing woven and knitted fabrics, creating fine irregularities on the surface of the fibers. It is believed that this is for the purpose of
ところが、衣料に関する消費者M識の高揚とともに、こ
れらの特性を満足しただけの織編物ではII腐なものと
なりつつあり、多様化、高級化に対応できない欠点がク
ローズアップされてきた。特にこれらの織編物にはふく
らみ、ドレープ性といった風合は付与しえなかった。However, with the rise in consumer awareness regarding clothing, woven and knitted fabrics that only satisfy these characteristics are becoming obsolete, and the drawbacks of not being able to respond to diversification and luxury have been highlighted. In particular, these woven and knitted fabrics could not be given any texture such as fullness or drapability.
一方、ポリエステル収縮差混繊糸を用いた織編物は、ふ
くらみとドレープ性およびソフト感を同時に付与するこ
とができることから重要視されており、これに関する技
術としては、特公昭55−22586号公報、特公昭5
B−3064号公報あるいは特開昭58−120816
号公報などに開示されている。これらのポリエステル収
縮差混繊糸はシルキー織編物を目的としたもので、絹の
ような光沢が不可欠であるため、酸化チタン等の艶消し
剤は全く含まないか、含んでいたとしてもわずかな量を
含んだポリエステルが用いられるのが通常であった。こ
のため当然のごとく透けを防止するといった点において
は劣っていた。On the other hand, woven and knitted fabrics using polyester differential shrinkage mixed fiber yarns are considered important because they can provide fullness, drapability, and a soft feel at the same time, and related technologies include Japanese Patent Publication No. 55-22586; Tokuko Showa 5
B-3064 publication or JP-A-58-120816
It is disclosed in the publication number etc. These polyester differential shrinkage blend yarns are intended for silky woven and knitted fabrics, and because a silk-like luster is essential, they do not contain matting agents such as titanium oxide at all, or even if they do contain them, they contain only a small amount. Typically, a polyester containing a certain amount was used. For this reason, it was naturally inferior in terms of preventing see-through.
この問題を解決する方法として収縮差渡織糸の収縮率の
大なる繊維群にのみ艶消し剤を含有させる技術が特開昭
61−275434 @公報に開示されている。この技
術によれば、収縮率の小なるm、m群にはMP!消し剤
を含有させず、含金属リン化合物とアルカリ土類金属化
合物を含有させることにより微細孔を生じせしめ、さら
に収縮率の大なる繊維群に艶消し剤を含有させることに
よって深色性、鮮明性に優れ、ソフトでふくらみがあっ
て、透けのない#1編物を提供する繊維を創出すること
が可能である。ところがかかる繊維による#1編物にお
いては織編物表面において浮き上がった状態にある収縮
率の小なるaim群に艶消し剤が含有されていないため
に、ミルキーな光沢がなく全体的な風合としては満足の
いくものではない。As a method for solving this problem, a technique is disclosed in JP-A No. 61-275434@, in which a matting agent is contained only in a group of fibers having a large shrinkage rate in a shrinkable cross weave yarn. According to this technology, MP! By not containing an erasing agent but containing a metal-containing phosphorus compound and an alkaline earth metal compound, fine pores are created, and by adding a matting agent to the fiber group with a high shrinkage rate, deep color and vividness can be achieved. It is possible to create fibers that have excellent elasticity and provide a #1 knitted fabric that is soft, full, and non-see-through. However, in the #1 knitted fabric made of such fibers, since no matting agent is contained in the aim group with a low shrinkage rate that floats on the surface of the woven or knitted fabric, there is no milky luster and the overall texture is satisfactory. It's not something you can do.
[発明が解決しようとする課題]
本発明は、かかる従来技術の問題点を解消し、透けを防
止し、ミルキーな光沢、ふくらみ、ドレープ性、ソフト
感に富み特に従来技術では創出しえなかった繊18なド
ライタッチ風合を有する薄地織編物を構成する糸条とし
て好適であるポリエステル収縮差混繊糸を得ることを目
的とするものである。[Problems to be Solved by the Invention] The present invention solves the problems of the prior art, prevents see-through, and provides milky luster, fullness, drapability, and a soft feel that could not be created using the prior art. The object of the present invention is to obtain a polyester shrinkage differential fiber yarn that is suitable as a yarn constituting a thin woven or knitted fabric having a dry touch feel of 18%.
[課題を解決するための手段]
本発明者らは前記した本発明の目的は、熱収縮率の異な
る少なくとも2種のgAN群からなり、沸水収縮率が3
2%以下で沸収DFLが5%以上28%以下である収縮
差混繊糸であって、該収縮差混繊糸を構成する繊維群の
うち少なくとも最も収縮率の小なる繊rff1群(以下
低収縮糸と称する)の全てが艶消し剤を1.3重量%以
上10.0重量%以下含有していることを特徴とするポ
リエステル収縮差混繊糸によって達成することができる
ことを見出した。[Means for Solving the Problems] The object of the present invention as described above by the present inventors is to provide a gAN group consisting of at least two types of gAN having different heat shrinkage rates, and a boiling water shrinkage rate of 3.
A shrinkage mixed fiber yarn having a boiling point DFL of 5% or more and 28% or less at a temperature of 2% or less, and at least the fibers rff1 group (hereinafter referred to as It has been found that this can be achieved by using a polyester differential shrinkage mixed yarn characterized in that all of the low shrinkage yarns (referred to as low shrinkage yarns) contain a matting agent in an amount of 1.3% by weight or more and 10.0% by weight or less.
本発明において、目標としているミルキーな光沢と従来
技術にはない繊細なドライタッチ風合を有し、なおかつ
透けが防止された薄地織編物を得るためには収縮差al
t糸を構成する低収縮糸の全てに艶消し剤を含有させる
ことが必要である。ただし艶消し剤含有量は1.3重層
%以上10.0重量%以下であることが必要である。艶
消し剤含有量が1.3重量%に満たないとミルキーな光
沢、繊1なドライタッチ風合および透けの防止(以下防
透は性と称する)のいずれの特性も満足しえない。なお
艶消し剤含有屋が2.0重量%以上になると特にミルキ
ーな光沢がよりマイルドになって好ましい。他方艶消し
剤含有量が10重量%を超えると、糸強度が低く製織時
もしくは製編時に毛羽などが発生し易くなる。In the present invention, in order to obtain a thin woven or knitted fabric that has the targeted milky luster and a delicate dry touch texture that is not found in the conventional technology, and is also prevented from being see-through, it is necessary to
It is necessary to contain a matting agent in all of the low shrinkage yarns that make up the T yarn. However, the content of the matting agent must be 1.3% to 10.0% by weight. If the matting agent content is less than 1.3% by weight, none of the characteristics of milky gloss, silky dry touch texture, and prevention of see-through (hereinafter referred to as "resistance") cannot be satisfied. It is preferable that the content of the matting agent is 2.0% by weight or more, since the milky gloss becomes milder. On the other hand, if the content of the matting agent exceeds 10% by weight, the yarn strength will be low and fuzz will easily occur during weaving or knitting.
また製糸工程における操業性の面からも、艶消し剤含有
量が101i最%を超えると紡糸時の濾材の目詰まりが
著しくなるために、長時間安定な紡糸が困難になる。な
お艶消し剤の含有量が7重量%以下となると糸の強度低
下がほとんどなくなるのでより好ましい。Also, from the viewpoint of operability in the spinning process, if the content of the matting agent exceeds the maximum 101%, clogging of the filter medium during spinning becomes significant, making stable spinning for a long period of time difficult. Note that it is more preferable that the content of the matting agent is 7% by weight or less, since there is almost no decrease in the strength of the yarn.
本発明の目標とする防透は性は、織編物を構成する収縮
差混繊糸の一部の単糸群が、特定量の艶消し剤を含有さ
せることにより達成できる。The anti-transparent property targeted by the present invention can be achieved by including a specific amount of a matting agent in some of the single yarn groups of the shrinkage mixed fiber yarns constituting the woven or knitted fabric.
ここにおいて、収縮差混繊糸の全ての繊維に艶消し剤を
1.3重量%以上10.0重量%以下含有させると防透
は性がさらに良好となり好ましい。Here, it is preferable that all the fibers of the differential shrinkage mixed yarn contain a matting agent in an amount of 1.3% by weight or more and 10.0% by weight or less, since the anti-transparent property is further improved.
ただし低収縮糸の場合と同様に艶消し剤含有量が1.3
重量%以下ではほとんど防透は性の効果はなく、また艶
消し剤含有量が10重量%を超えると、糸強度が低く製
編織時に毛羽などが発生し易く、また操業性の面からも
艶消し剤含有量が10重量%を超えると紡糸時の濾材の
目詰まりが著しくなるために、長時間安定な紡糸が困難
になる。このため艶消し剤含有屋は10重量%以下が好
ましい。また艶消し剤の含有量が7重量%以下となると
糸の強度低下がほとんどなくな゛るのでざらに好ましい
。However, as in the case of low shrinkage yarn, the matting agent content is 1.3
If the content of the matting agent is less than 10% by weight, the yarn strength will be low and fuzz will easily occur during weaving, and the matting agent will not be as effective in terms of workability. If the content of the erasing agent exceeds 10% by weight, clogging of the filter medium during spinning becomes significant, making stable spinning for a long time difficult. Therefore, the content of the matting agent is preferably 10% by weight or less. Further, it is particularly preferable that the content of the matting agent is 7% by weight or less, since there is almost no decrease in the strength of the yarn.
本発明において目標としているソフト感を付与させるに
は、収縮差混繊糸の洲本収縮率(以下BWSと称するン
が32%以下である必要がある。BWSが32%を越え
た場合には、得られた織編物は粗硬感が強すぎて商品価
値のないものとなる。なあ、ソフト感をより高度なもの
とするために、BWSは28%以下が好ましい。In order to impart the soft feel targeted in the present invention, the Sumoto shrinkage rate (hereinafter referred to as BWS) of the differential shrinkage blend yarn must be 32% or less. If the BWS exceeds 32%, The obtained woven or knitted fabric has too strong a rough and hard feel and has no commercial value.In order to achieve a higher level of soft feel, the BWS is preferably 28% or less.
本発明において、目標としている豊かなふくらみおよび
繊細なドライタッチ風合を付与させるには、収縮差混繊
糸の沸収DFL (以下DFLと称する)が5%以上2
8%以下である必要がある。特にvanなドライタッチ
風合を織編物に付与させるには、既に述べたとおり収縮
差混繊糸を構成する低収縮糸の全てに艶消し剤を特定量
含有させただけでは必要条件を満たしたにすぎず、更に
DELが5%以上28%以下である必要がある。DFL
が5%未満の場合、得られた織編物は十分なふくらみの
ないペーパーライクなものになってしまい、またドライ
タッチ風合も通常糸と変わらないものとなってしまい本
発明る繊細なドライタッチ風合は付与し得ない。In the present invention, in order to provide the targeted rich fullness and delicate dry touch texture, the boiling point DFL (hereinafter referred to as DFL) of the differential shrinkage blend yarn must be 5% or more.
It needs to be 8% or less. In particular, in order to impart a vanishing dry-touch texture to a woven or knitted fabric, simply adding a specific amount of a matting agent to all of the low-shrinkage yarns that make up the differential shrinkage blend yarn does not satisfy the necessary conditions. Furthermore, the DEL must be 5% or more and 28% or less. D.F.L.
If it is less than 5%, the resulting woven or knitted fabric will be paper-like without sufficient bulge, and the dry touch texture will be the same as that of ordinary yarn. Texture cannot be imparted.
ここにおいてDFLが9%以上となるとふくらみがより
豊かになって好ましい。他方DFLが28%を越えると
織編物の表面で低収縮糸が座屈してしまい、表面外観を
均斉としがたくなりふくらみのみならず、W!編物の全
般的な風合の低下が顕著になり、本発明の目的とする高
度な風合を有する織編物を得ることが不可能である。Here, when the DFL is 9% or more, the swelling becomes richer, which is preferable. On the other hand, if the DFL exceeds 28%, the low shrinkage yarn will buckle on the surface of the woven or knitted material, making it difficult to maintain a uniform surface appearance, resulting in not only fullness but also W! The overall feel of the knitted fabric deteriorates significantly, making it impossible to obtain a woven or knitted fabric with the high level of feel that is the objective of the present invention.
ここにおいて、DELが23%以下の場合、taIIl
なドライタッチ風合がより高度なものとなって好ましい
。なおりWS、DFLの測定法に関しては後述する。Here, if DEL is 23% or less, taIIl
The dry touch texture is more advanced, which is preferable. The method for measuring WS and DFL will be described later.
本発明の特徴は収縮差混繊糸の低収縮糸に艶消し剤を含
有せしめた点にある。収縮差混繊糸中の低収縮糸は織編
物の表面において浮き上がった状態にあり、これは織編
物中の通常糸に比べ特異的な状態にあるといえる。本発
明の目標とする繊細なドライタッチ風合は、艶消し剤に
より微細な凹凸を有した繊維を織編物の表面上でこのよ
うな特異的な状態にすることにより創出することが可能
である。この原因は明らかではないが、アルカリ減量処
理による艶消し剤の脱落により微細な凹凸を有し、この
ために触ったときの単位繊度あたりの接触面積が小さく
、また艶消し剤の表面凝着エネルギーが小さいために、
単糸の表面摩擦特性が大きく変化しているIIAMが織
編物の表面において浮き上がり、比較的動きやすい状態
にあるために起こるものと考えられる。The feature of the present invention is that the low shrinkage yarn of the differential shrinkage mixed fiber yarn contains a matting agent. The low shrinkage yarns in the differential shrinkage blend yarn are in a floating state on the surface of the woven or knitted fabric, and this can be said to be in a unique state compared to normal yarns in the woven or knitted fabric. The delicate dry-touch texture that is the goal of the present invention can be created by using a matting agent to bring the fibers, which have minute irregularities, into such a specific state on the surface of the woven or knitted fabric. . The cause of this is not clear, but due to the shedding of the matting agent due to alkali weight loss treatment, there are fine irregularities, which results in a small contact area per unit fineness when touched, and the surface adhesion energy of the matting agent. Because of the small
This is thought to occur because IIAM, whose surface frictional properties of the single yarn have changed significantly, floats on the surface of the woven or knitted fabric and is relatively mobile.
本発明の収縮差混繊糸はw4維形成性の優れたポリエス
テルからなることが必要で、好ましくはポリエチレンテ
レフタレートが良い。このポリエステルあるいはポリエ
チレンテレフタレートは製造工程において副生成される
範囲内でジエチレングリコールなどを主鎖に含んでいて
もかまわない。特に収縮差混繊糸の製造方法の中で生産
性の点で最も優れた紡糸混繊方式をとることが可能とな
るので、低収縮糸をポリエステルとし、収縮率の最も大
なるR維群(以下高収縮糸と称する)を第三成分を共重
合せしめた共重合ポリエステルとすることが好ましい。The differential shrinkage mixed fiber yarn of the present invention needs to be made of polyester with excellent W4 fiber formation properties, and polyethylene terephthalate is preferable. This polyester or polyethylene terephthalate may contain diethylene glycol or the like in its main chain as long as it is by-produced during the manufacturing process. In particular, it is possible to use the spinning blend method, which is the most excellent in terms of productivity among the methods for producing differential shrinkage blend yarns, so polyester is used as the low shrinkage yarn, and the R fiber group (with the highest shrinkage rate) ( It is preferable that the copolymerized polyester (hereinafter referred to as high shrinkage yarn) is copolymerized with a third component.
ここにおいて安定な製糸が可能であって、なおかつ既に
述べた収縮差混繊糸の収縮特性が容易に得られるため、
共重合量は5モル%以上18モル%以下とすることがよ
り好ましい。Stable yarn spinning is possible here, and the shrinkage characteristics of the shrinkage mixed fiber yarn described above can be easily obtained.
The amount of copolymerization is more preferably 5 mol% or more and 18 mol% or less.
更に、この高収縮系に用いられる共重合ポリエステルを
、特定の共重合ポリエステルとすることにより、アルカ
リ減量処理を単位表面積当たりのアルカリ減量速度比で
低収縮糸よりも高収縮糸の方が1.3以上3.1以下大
きくすると好ましい。高収縮糸と低収縮糸との間に、こ
のようなアルカリ減量速度差を有する収縮差混繊糸は、
織編物の仕上げ工程において通常行なわれるアルカリ減
量処理により、繊細なドライタッチ風合とドレープ性を
同時に最も良好な状態とすることが容易になる。Furthermore, by using a specific copolymerized polyester as the copolymerized polyester used in this high-shrinkage system, the alkali weight loss rate ratio per unit surface area of the high-shrinkage yarn is higher than that of the low-shrinkage yarn. It is preferable to increase it by 3 or more and 3.1 or less. Differential shrinkage blend yarns with such a difference in alkali weight loss rate between high shrinkage yarns and low shrinkage yarns are
The alkaline weight loss treatment that is usually carried out in the finishing process of woven or knitted fabrics makes it easy to achieve the best possible delicate dry touch texture and drape properties at the same time.
なお、高収縮系と低収縮糸とのアルカリ減量速度の違い
の尺度である、単位表面積当たりのアルカリ減量速度比
の測定法に関しては後述する。The method for measuring the alkali weight loss rate ratio per unit surface area, which is a measure of the difference in alkali weight loss rate between high shrinkage yarns and low shrinkage yarns, will be described later.
通常、収縮差混繊糸の高収縮糸に用いられる共重合ポリ
エステルの第三成分としては、シュウ酸、セバシン酸、
フタル酸、イソフタル酸などのジカルボン酸類、ジエチ
レングリコール、ポリエチレングリコール、ネオペンチ
ルグリコール等のグ1)コール類の他、ビスフェノール
A、ビスフェノールスルフォン等や、これらのうちの2
種以上の第三成分を同時に共重合させたものが挙げられ
る。本発明における特定の共重合ポリエステルとしては
、これらの共重合ポリエステルのうちアルカリ減量速度
がポリエステルのアルカリ減量速度よりも単位表面積当
たりのアルカリ減量速度比で1.3以上3.1以下大ぎ
くするものを好適に選択できる。特にビスフェノールA
1.0モル%以上とイソフタルfi3.0モル%以上
をともに、第三成分を共重合した共重合ポリエステルを
高収縮糸とする収縮差混繊糸は、製糸が容易であり、最
終製品である#1編物のふくらみがより高度なものとな
るので好ましい。Usually, the third component of copolyester used for high shrinkage yarn of differential shrinkage blend yarn is oxalic acid, sebacic acid,
In addition to dicarboxylic acids such as phthalic acid and isophthalic acid, glycols such as diethylene glycol, polyethylene glycol, and neopentyl glycol, bisphenol A, bisphenol sulfone, etc., and two of these.
Examples include those in which more than one type of third component is copolymerized at the same time. Specific copolymerized polyesters in the present invention include those whose alkali weight loss rate is greater than the alkali weight loss rate of the polyester by 1.3 or more and 3.1 or less in terms of alkali weight loss rate ratio per unit surface area. can be suitably selected. Especially bisphenol A
A differential shrinkage blend yarn in which a copolymerized polyester containing 1.0 mol% or more and 3.0 mol% or more of isophthalic fi and a third component is copolymerized as a high shrinkage yarn is easy to spin and is a final product. #1 is preferable because the knitted fabric has a higher degree of fullness.
ざらに、ビスフェノールA 1.0モル%以上4.8モ
ル%以下とイソフタルm3.0モル%以上をともに第三
成分として共重合した共重合ポリエステルを高収縮糸と
する収縮差混繊糸は、最終製品である織編物の退色堅牢
度が良好となり好ましい。なお高収縮糸と低収縮糸を構
成する共重合ポリエステルおよびポリエステルの固有粘
度の差は0.03以下であることが好ましく、高収縮系
がより高い固有粘度であることがより好ましい。この差
が0.03を越えると、収縮差混繊糸にクルミが発生し
製糸性および製織性、製編性が悪化する傾向がある。こ
こにおいて、固有粘度は25°Cオルソクロロフェノー
ル中で測定した1直である。In general, a differential shrinkage blend yarn using a copolymerized polyester copolymerized with 1.0 mol% or more of bisphenol A and 4.8 mol% or less of bisphenol A and 3.0 mol% or more of isophthalic m as a third component is used as a high shrinkage yarn. This is preferable because the fading fastness of the final product, woven or knitted product, is good. Note that the difference in intrinsic viscosity between the copolymerized polyester and polyester constituting the high-shrinkage yarn and the low-shrinkage yarn is preferably 0.03 or less, and it is more preferable that the high-shrinkage yarn has a higher intrinsic viscosity. When this difference exceeds 0.03, walnuts occur in the differentially shrinkage blended yarn, which tends to deteriorate spinning, weaving, and knitting properties. Intrinsic viscosity here is one unit measured in orthochlorophenol at 25°C.
本発明に用いられる艶消し剤としては、酸化チタン、酸
化ジルコニウム、酸化マグネシウム、酸化アルミニウム
、酸化ケイ素、酸化アンチモン、酸化亜鉛、タングステ
ン酸鉛、タングステン酸カルシウム、炭酸カルシウム等
、本発明の効果を発現し、ポリエステルに安定して分散
できるものであればいずれもかまわないが、分散性の面
から、酸化チタン、酸化ケイ素、酸化亜鉛、炭酸カルシ
ウムが好ましい。The matting agents used in the present invention include titanium oxide, zirconium oxide, magnesium oxide, aluminum oxide, silicon oxide, antimony oxide, zinc oxide, lead tungstate, calcium tungstate, calcium carbonate, etc., which exhibit the effects of the present invention. However, any material may be used as long as it can be stably dispersed in polyester, but from the viewpoint of dispersibility, titanium oxide, silicon oxide, zinc oxide, and calcium carbonate are preferable.
添加する艶消し剤の平均粒径は、分散性の観点から、1
μm以下が好ましく、更に好ましくは0.7μIll以
下である。更に製糸性の観点から最大粒径は、5μff
i以下が好ましく、更に好ましくは3μm以下である。From the viewpoint of dispersibility, the average particle size of the matting agent to be added is 1.
The thickness is preferably .mu.m or less, more preferably 0.7 .mu.Ill or less. Furthermore, from the viewpoint of spinning properties, the maximum particle size is 5 μff.
i or less is preferable, and more preferably 3 μm or less.
本発明の収縮差混繊糸は、熱収縮率の異なる少なくとも
2種のm雄部からなることが必要であるが、製糸が容易
なことから2種のl!維群であることが好ましい。また
、収縮差混繊糸中の低収縮糸の単糸数は、高収縮糸の単
糸数以上とすると、ふくらみ及びamなドライタッチ風
合がさらに良好となって好ましい。また単糸の断面形状
に関しては高収縮糸は特に限定はないが、低収縮糸はミ
ルキーな光沢を付与する上で三角断面、T壁断面、三葉
断面などの異形断面であることが好ましい。The differential shrinkage mixed fiber yarn of the present invention needs to be composed of at least two types of m-male portions having different heat shrinkage rates, but since it is easy to spin, there are two types of l-male portions. Preferably, it is a group of fibers. Further, it is preferable that the number of single yarns of the low shrinkage yarns in the differential shrinkage yarn is equal to or greater than the number of single yarns of the high shrinkage yarns, as this will further improve the fluffiness and the ampery dry touch feel. There are no particular limitations on the cross-sectional shape of the single yarn for high-shrinkage yarns, but low-shrinkage yarns preferably have irregular cross-sections such as triangular cross-sections, T-wall cross-sections, and trilobal cross-sections in order to impart a milky luster.
本発明の収縮差混繊糸は、例えば、特公昭51−306
20号公報や特開昭49−72449号公報などに示さ
れるような通常の混繊紡糸と延伸により得られる。この
製糸工程において、製編織における工程通過性を向上さ
せるために流体交絡処理を付与することが好ましい。た
だし交絡点がtjfifm物表面における低収縮糸の浮
き上がりをおさえるために、過度の交絡は風合の低下を
もたらす。The shrinkage mixed fiber yarn of the present invention can be used, for example, in Japanese Patent Publication No. 51-306
It can be obtained by conventional mixed fiber spinning and drawing as shown in Japanese Patent Application Laid-Open No. 49-72449. In this yarn spinning process, it is preferable to apply fluid entanglement treatment to improve process passability in weaving, knitting and weaving. However, since the intertwining points prevent the low shrinkage yarn from lifting up on the surface of the tjfifm object, excessive intertwining results in a deterioration of the texture.
好ましい交絡度の範囲は5〜60コ/mである。The preferred degree of entanglement is in the range of 5 to 60 pieces/m.
交絡度が5コ/mに達しない場合、工程通過性を向上の
程度が実用のレベルに達しないため好ましくない。なお
、交絡度の測定法は特開昭48−28708号公報に示
された方法に従う。If the degree of entanglement does not reach 5 co/m, the degree of improvement in process passability will not reach a practical level, which is not preferable. Note that the method for measuring the degree of entanglement follows the method disclosed in Japanese Patent Application Laid-Open No. 48-28708.
ここで、本発明における収縮差混繊糸の糸特性の測定法
に関して述べる。Here, a method for measuring the yarn properties of the differential shrinkage mixed fiber yarn in the present invention will be described.
■沈水収縮率(BWS>
収縮差混繊糸を100 mQ/dの荷重下で試料長(L
o>を測定したのち無荷重の状態で20分間沸水処理を
行なう。処理後100 mMdの荷重下で試料長(Ll
〉を測定する。BWSは■式で表される。■ Submerged shrinkage rate (BWS) The sample length (L
After measuring o>, a boiling water treatment is performed for 20 minutes under no load. After treatment, the sample length (Ll
>Measure. BWS is expressed by the formula ■.
BWS= (L o−11) /L o xloo(%
〉■
■沸収DFL (DEL>
収縮差混繊糸を高収縮糸と低収縮糸とに分けた後、それ
ぞれ100 mMdの荷重下で試料長(Lho、Lp
o)を測定し、無荷重の状態で20分聞沸水処理を行な
う。処理後100 mg/dの荷重下で試料長(Lh+
、Ll+)を測定する。■の方法に従ってそれぞれの導
水収縮率(BWSh、BWSl)を算出する。BWS= (L o−11) /L o xloo(%
〉 ■ ■ Boiling yield DFL (DEL> After dividing the differential shrinkage mixed fiber yarn into high shrinkage yarn and low shrinkage yarn, the sample lengths (Lho, Lp
o) was measured, and treated with boiling water for 20 minutes under no load. After treatment, the sample length (Lh+
, Ll+). Calculate each water conduction shrinkage rate (BWSh, BWSl) according to method (2).
DFLは■式で表される。DFL is expressed by the formula (■).
DFL= (BWSh−BWSx )/ (100−B
WSh)X100 (%〉・・・・・・■■単単位面
面積当りのアルカリ減量速度比■の処理の後、試料を無
荷重の状態で用乾し、次いで2mMdの荷重下で170
℃の乾熱処理を3分間行う。この処理の後、試料の断面
写真をi彰する。次いで3.5%の水酸化ナトリウム水
溶液で沸りn!温度にて処理し、15%〜30%減量す
る。さらにその試料断面写真を撮影して、断面積の変化
から高収縮糸と低収縮糸のアルカリ減量速度比を算出す
る。さらに高収縮糸と低収縮糸の単糸繊度比、密度比か
らアルカリ減H!1理前の両者の表面積比を算出する。DFL= (BWSh-BWSx)/(100-B
WSh)
Dry heat treatment at ℃ is performed for 3 minutes. After this treatment, a cross-sectional photograph of the sample is presented. Next, boil n! with 3.5% sodium hydroxide aqueous solution. Process at temperature to reduce weight by 15% to 30%. Furthermore, a cross-sectional photograph of the sample is taken, and the alkali weight loss rate ratio of the high-shrinkage yarn and the low-shrinkage yarn is calculated from the change in cross-sectional area. Furthermore, alkali reduction H is obtained from the single yarn fineness ratio and density ratio of high shrinkage yarn and low shrinkage yarn! 1. Calculate the surface area ratio of both.
この2つの比から単位表面積当りのアルカリ減量速度比
率を算出する。From these two ratios, the alkali weight loss rate ratio per unit surface area is calculated.
[実施例] 以下、具体例をあげて本発明を説明する。[Example] The present invention will be explained below by giving specific examples.
実施例1
テレフタル酸/エチレングリコールスラリを用いてエス
テル化反応を行なった後、平均粒径0.5μmで最大粒
径2μmの酸化チタンのエチレングリコール溶液(13
,5CI/100mQ)を添ハUし、通常の重合反応を
行ない酸化チタン含有量の異なるポリエチレンテレフタ
レートのチップ(チップI>8種を得た。他方テレフタ
ル酸/エチレングリコール及びイソフタル酸/エチレン
グリコールスラリを用い、エステル化反応を行なった後
、ビスフェノール八と平均粒径0.5μmで最大粒径2
μmの酸化チタンのエチレンクリ] −ル溶液(13,
5g/100mQ)を添7JOt、、通常の重合反応を
行ない酸化チタン含有量の異なるイソフタル酸10.5
モル%、ビスフェノールA3.5モル%共重合ポリエチ
レンテレフタレートのチップ(チップII)2種を得た
。このようにして得られたチップ■とチップ■を表1の
水準NQ1〜水準Nα9に示す種々の組合せ、吐出孔径
の異なる紡糸口金を装着した紡糸閑により、紡糸温度2
90℃、紡糸速度1300 m7分で混繊未延伸糸を紡
糸した、さらにこの混繊未延伸糸を延伸速度800 m
7分でホットロール(温度90’C)−熱板(温度10
0℃〜180℃)の方式により延伸し、表1水lN01
〜水準NQ9に示す収縮特性をもつ75デニール36フ
イラメント(高収縮糸二三角断面、37,5デニール1
8フイラメント、低収縮糸二三角断面、37.5デニー
ル18フイラメント)の収縮差混繊糸を得た。なお延伸
の際にはエア交絡を施し20コ/mの交絡を付与させ、
延伸倍率は延伸糸の伸度が30%〜40%の範囲になる
ように調整した。また高収縮糸の固有粘度は0.85で
、低収縮糸の固有粘度は0.64であった。Example 1 After carrying out an esterification reaction using a terephthalic acid/ethylene glycol slurry, an ethylene glycol solution of titanium oxide (13
, 5CI/100mQ) was added, and a normal polymerization reaction was carried out to obtain polyethylene terephthalate chips with different titanium oxide contents (Chip I > 8 types.On the other hand, terephthalic acid/ethylene glycol and isophthalic acid/ethylene glycol slurries were added. After carrying out the esterification reaction using bisphenol 8, the average particle size is 0.5 μm and the maximum particle size is 2.
μm of titanium oxide in ethylene glycol solution (13,
5g/100mQ) was added to 7JOt, and 10.5JOt of isophthalic acid with different titanium oxide contents was subjected to a normal polymerization reaction.
Two types of chips (Chip II) of copolymerized polyethylene terephthalate containing 3.5 mol% of bisphenol A were obtained. The chips ■ and chips ■ obtained in this way were combined into various combinations shown in levels NQ1 to Nα9 in Table 1, and were spun at a spinning temperature of 2 using a spinning machine equipped with spinnerets having different discharge hole diameters.
The mixed fiber undrawn yarn was spun at 90°C and a spinning speed of 1300 m for 7 minutes, and the mixed fiber undrawn yarn was further drawn at a drawing speed of 800 m.
Hot roll (temperature 90'C) - hot plate (temperature 10'C) in 7 minutes
Table 1 Water lN01
~75 denier 36 filament with shrinkage characteristics shown in level NQ9 (high shrinkage thread two triangular cross section, 37.5 denier 1
A differential shrinkage mixed fiber yarn with 8 filaments, low shrinkage yarn, two triangular cross sections, 37.5 denier (18 filaments) was obtained. In addition, during stretching, air entanglement was applied to give 20 entanglements/m,
The stretching ratio was adjusted so that the elongation of the drawn yarn was in the range of 30% to 40%. Further, the intrinsic viscosity of the high shrinkage yarn was 0.85, and the intrinsic viscosity of the low shrinkage yarn was 0.64.
なお表1には単位表面積当たりのアルカリ減量速度比の
測定結果も示した。Table 1 also shows the measurement results of the alkali weight loss rate ratio per unit surface area.
この糸を経糸及び緯糸として用い、織り密度をそれぞれ
105本/インチ、85本/インチで製織し平織物とし
た後、98℃熱水でリラックス精練、170℃で仕上げ
セットし、更に減量率23〜25%のアルカリ減量処理
を行ない織布とした。Using this yarn as the warp and weft, we weave at a weaving density of 105 yarns/inch and 85 yarns/inch, respectively, to make a plain weave. After relaxing scouring with hot water at 98°C, finishing and setting at 170°C, and further reducing the weight loss by 23 The woven fabric was subjected to an alkali weight loss treatment of ~25%.
この織布を用いてふくらみ、ソフト感、!a細なドライ
タッチ風合、ミルキーな光沢、ドレープ性を官能評価に
より判定した。This woven fabric gives you a full and soft feeling! A fine dry touch texture, milky luster, and drapability were evaluated by sensory evaluation.
なお、防透は性の判定は、スガ試験機株式会社製SMカ
ラーコンピューターを用いて、この織布の背後に、白色
体及び黒色体を置いて測定したそれぞれのL値の差を3
ランクに分は防透は性の尺度とした。The anti-transparent property is determined by measuring the difference in L value between a white body and a black body by placing a white body and a black body behind this woven fabric using an SM color computer manufactured by Suga Test Instruments Co., Ltd.
In terms of rank, impermeability was used as a measure of sex.
表1において、水準Nα1.2および9は本発明の効果
を確認するための比較例である。In Table 1, levels Nα1.2 and 9 are comparative examples for confirming the effects of the present invention.
比較例である水1lP=Nα1ではaimなドライタッ
チ風合、ミルキーな光沢、防透は性が満足できるもので
はない。これは低収縮糸中の酸化チタン量が少なすぎる
ためである。In the comparative example of water 1lP=Nα1, the aim dry touch texture, milky gloss, and anti-transparency properties are not satisfactory. This is because the amount of titanium oxide in the low shrinkage yarn is too small.
比較例である水準Nα2においても、繊IBなドライタ
ッチ風合、ミルキーな光沢が満足できるものではない。Even at level Nα2, which is a comparative example, the fiber IB dry touch texture and milky gloss are not satisfactory.
これも低収縮糸中の酸化チタン量が少なすぎるためであ
る。This is also because the amount of titanium oxide in the low shrinkage yarn is too small.
比較例である水準Nα9は、表1に示した項目において
は良好であるが、織布の引き裂き強力が低く、また製織
時に発生した多数の毛羽のために品位が低下し、商品価
値のないものとなってしまった。また、紡糸時の濾材層
の目詰まりによる濾圧上昇が大きく、5時間以上の安定
な紡糸が困難であった。Level Nα9, which is a comparative example, is good in terms of the items shown in Table 1, but the tearing strength of the woven fabric is low, and the quality is degraded due to a large number of fuzz generated during weaving, and it has no commercial value. It became. Furthermore, the filtration pressure increased significantly due to clogging of the filter layer during spinning, making stable spinning for 5 hours or more difficult.
本発明の実施例である水準1’IQ3〜水準Nα8は、
良好な風合が得られている。ただし水準NQ7および水
準Nα8の織布においては収縮差混繊糸の強度低下によ
ると考えられる引き裂き強力の若干の低下が見られた。Level 1'IQ3 to level Nα8 which are examples of the present invention are as follows:
A good texture is obtained. However, in the woven fabrics of level NQ7 and level Nα8, a slight decrease in tearing strength was observed, which is considered to be due to a decrease in the strength of the differentially shrinkage mixed fiber yarn.
(以下余白)
実施例2
テレフタル酸/エチレングリコール及びイソフタル酸/
エチレングリコールスラリを用い、エステル化反応を行
なった後、ビスフェノール八と平均粒径0.5μmで最
大粒径2μmの酸化チタンのエチレングリコール)8液
(13,5CI/100mQ>を添加して通常の重合反
応を行ない、酸化チタンを3.F41%含んだ4種の共
重合ポリエチレンテレフタレートのチップ(チップ■)
を得た。これら種々のチップ■と実施例1水準Nα5の
チップエ(酸化チタン3.5重量%含有)とを表2に示
す組合せで、実施例1の方法により製糸、製織し織布と
し同様の評価を行なった。(Left below) Example 2 Terephthalic acid/ethylene glycol and isophthalic acid/
After carrying out an esterification reaction using an ethylene glycol slurry, 8 liquids (13,5CI/100mQ> of ethylene glycol of titanium oxide with an average particle size of 0.5 μm and a maximum particle size of 2 μm) and bisphenol 8 were added. Four types of copolymerized polyethylene terephthalate chips containing 3.F and 41% titanium oxide after polymerization reaction (chip ■)
I got it. Using the combinations shown in Table 2 of these various chips (1) and Chip A (containing 3.5% by weight of titanium oxide) at the level Nα5 of Example 1, yarn was spun and woven according to the method of Example 1, and woven fabrics were used for the same evaluation. Ta.
ただし、水準No、19については、アルカリ減員率を
19%におさえ、他の工程は実施例1の方法に従い同様
の評価を行なった。However, for level No. 19, the alkali reduction rate was kept at 19%, and the other steps were evaluated in the same manner as in Example 1.
表2において、水準N(110,16および17は本発
明の効果を確認するための比較例である。In Table 2, levels N (110, 16, and 17 are comparative examples for confirming the effects of the present invention).
比較例である水準Nα10は1!細なドライタッチ及び
ふくらみが満足できるものではない。これはDFLが不
足しているためである。In the comparative example, the level Nα10 is 1! Fine dry touch and swelling are not satisfactory. This is due to the lack of DFL.
比較例である水準N016は、繊細なドライタッチ及び
ふくらみが満足できるものではない。Level No. 016, which is a comparative example, is not satisfactory in terms of delicate dry touch and swelling.
また織物表面において低収縮糸が座屈がみられ、風合が
かなり悪化していた。これはDFLが大きすぎるためで
ある。In addition, buckling of the low shrinkage yarns was observed on the surface of the fabric, and the texture was considerably deteriorated. This is because DFL is too large.
比較例である水INα17は、繊細なドライタッチ、ふ
くらみ及びソフト感が満足できるものではない。また水
準Nα16と同様に織物表面において低収縮糸が座屈が
みられ、風合がかなり悪化していた。これはDFL、B
SWが大きすぎるためである。Water INα17, which is a comparative example, is not satisfactory in terms of delicate dry touch, fullness, and soft feel. Also, as with level Nα16, buckling of the low shrinkage yarns was observed on the surface of the fabric, and the feel was considerably deteriorated. This is DFL, B
This is because SW is too large.
本発明の実施例である水準Nα11〜15.18および
19は、いずれも良好な風合を有している。特に水準N
α12は良い風合を持った織物であった。水準Nα18
はほぼ良好な風合を持った織物であったが、若干繊細な
ドライタッチが低下ぎみであった。Levels Nα11 to Nα15.18 and 19, which are examples of the present invention, all have good texture. Especially level N
α12 was a fabric with a good texture. Level Nα18
The fabric had almost good texture, but the slightly delicate dry touch was on the verge of deterioration.
なお、水準No、13〜19は他の水準に比べ退色堅牢
度が若干低下した。In addition, the fading fastness of level Nos. 13 to 19 was slightly lower than that of the other levels.
[発明の効果コ
本発明は収縮差混繊糸の収縮特性を特定するとともに、
低収縮糸群に艶消し剤を含有せしめることによって、透
けを防止し、ミルキーな光沢、ふくらみ、ドレープ性、
ソフト感に富み独特なハリ、コシをもっており、特に従
来技術では創出しえなかったしっとりした繊細なドライ
タッチ風合を有する織編物を構成する糸条として好適な
ポリエステル収縮差混繊糸とするものである。すなわち
、従来技術では酸化チタン等の粒子を添加させた。*維
をアルカリ減退処理することでドライタッチ風合を得る
ことはできたもののサラッとしたタッチのものしか得ら
れず、本発明の収縮差混繊糸により得られるしつとりし
た繊細なタッチは、従来技術からは予期できない新しい
風合である。[Effects of the Invention] The present invention specifies the shrinkage characteristics of differential shrinkage mixed fiber yarns, and
By incorporating a matting agent into the low-shrink yarn group, it prevents see-through and creates a milky luster, fullness, drapability,
A polyester differential shrinkage blend yarn that is rich in softness and has a unique firmness and stiffness, and is especially suitable as yarn for composing woven and knitted fabrics that have a moist and delicate dry touch texture that could not be created with conventional technology. It is. That is, in the prior art, particles of titanium oxide or the like were added. *Although it was possible to obtain a dry touch texture by subjecting the fibers to alkali reduction treatment, only a smooth touch was obtained; This is a new texture that cannot be expected from conventional technology.
Claims (3)
り、沸水収縮率が32%以下で沸収DFLが5%以上2
8%以下である収縮差混繊糸であって、該収縮差混繊糸
を構成する繊維群のうち少なくとも最も収縮率の小なる
繊維群の全てが艶消し剤を1.3重量%以上10.0重
量%以下含有していることを特徴とするポリエステル収
縮差混繊糸。(1) Consisting of at least two types of fiber groups with different heat shrinkage rates, boiling water shrinkage rate is 32% or less and boiling point DFL is 5% or more2
A shrinkage mixed fiber yarn having a shrinkage ratio of 8% or less, at least all of the fiber groups having the smallest shrinkage percentage among the fiber groups constituting the shrinkage mixed fiber yarn contain a matting agent of 1.3% by weight or more. A polyester shrinkage differential blend yarn characterized by containing .0% by weight or less.
を1.3重量%以上10.0重量%以下含有しているこ
とを特徴とする請求項(1)記載のポリエステル収縮差
混繊糸。(2) The shrinkable polyester according to claim (1), wherein all the fiber groups constituting the differential shrinkage blend yarn contain a matting agent of 1.3% by weight or more and 10.0% by weight or less. Differential blend yarn.
群はポリエステルとし、収縮率の最も大なる繊維群は第
三成分を5モル%以上18モル%以下共重合した共重合
ポリエステルとすることを特徴とする請求項(1)また
は(2)記載のポリエステル収縮差混繊糸。(3) The fiber group with the smallest shrinkage percentage constituting the differential shrinkage mixed fiber yarn is polyester, and the fiber group with the largest shrinkage percentage is a copolymerized polyester copolymerized with a third component of 5 mol% or more and 18 mol% or less. The polyester differential shrinkage mixed fiber yarn according to claim (1) or (2), characterized in that:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1190279A JPH0359130A (en) | 1989-07-21 | 1989-07-21 | Polyester blended yarn having different shrinkage |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1190279A JPH0359130A (en) | 1989-07-21 | 1989-07-21 | Polyester blended yarn having different shrinkage |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0359130A true JPH0359130A (en) | 1991-03-14 |
Family
ID=16255521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1190279A Pending JPH0359130A (en) | 1989-07-21 | 1989-07-21 | Polyester blended yarn having different shrinkage |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0359130A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05239726A (en) * | 1992-02-21 | 1993-09-17 | Teijin Ltd | Sensible bulky yarn |
| JP2002302835A (en) * | 2001-04-04 | 2002-10-18 | Nippon Ester Co Ltd | Heteroshrinkable polyester combined filament yarn |
| JP2007009369A (en) * | 2005-06-30 | 2007-01-18 | Toray Ind Inc | Woven knitted fabric made of blended yarn |
| JP2022045950A (en) * | 2020-09-10 | 2022-03-23 | クラレトレーディング株式会社 | Different shrinkage mixed yarn and fabric made from it |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59228014A (en) * | 1983-06-03 | 1984-12-21 | Toyobo Co Ltd | Silky polyester filament yarn |
| JPS6113009A (en) * | 1984-06-29 | 1986-01-21 | 川崎重工業株式会社 | Connection of steel pipe structural member |
| JPS63196735A (en) * | 1987-02-10 | 1988-08-15 | 帝人株式会社 | Production of spun like processed yarn |
-
1989
- 1989-07-21 JP JP1190279A patent/JPH0359130A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59228014A (en) * | 1983-06-03 | 1984-12-21 | Toyobo Co Ltd | Silky polyester filament yarn |
| JPS6113009A (en) * | 1984-06-29 | 1986-01-21 | 川崎重工業株式会社 | Connection of steel pipe structural member |
| JPS63196735A (en) * | 1987-02-10 | 1988-08-15 | 帝人株式会社 | Production of spun like processed yarn |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05239726A (en) * | 1992-02-21 | 1993-09-17 | Teijin Ltd | Sensible bulky yarn |
| JP2002302835A (en) * | 2001-04-04 | 2002-10-18 | Nippon Ester Co Ltd | Heteroshrinkable polyester combined filament yarn |
| JP2007009369A (en) * | 2005-06-30 | 2007-01-18 | Toray Ind Inc | Woven knitted fabric made of blended yarn |
| JP2022045950A (en) * | 2020-09-10 | 2022-03-23 | クラレトレーディング株式会社 | Different shrinkage mixed yarn and fabric made from it |
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