JP3666616B2 - Method for producing high bulk and thick woven fabric - Google Patents

Method for producing high bulk and thick woven fabric Download PDF

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Publication number
JP3666616B2
JP3666616B2 JP08392396A JP8392396A JP3666616B2 JP 3666616 B2 JP3666616 B2 JP 3666616B2 JP 08392396 A JP08392396 A JP 08392396A JP 8392396 A JP8392396 A JP 8392396A JP 3666616 B2 JP3666616 B2 JP 3666616B2
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Japan
Prior art keywords
yarn
polyester fiber
knitted fabric
producing
fiber yarn
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JPH09273046A (en
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全央 松田
雄一郎 表
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Toyobo Co Ltd
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Toyobo Co Ltd
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  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
  • Woven Fabrics (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は、ソフトでふくらみのある、優れた風合いを有する嵩高厚地織編物の製造方法に関し、具体的には自己伸長糸と収縮糸の混繊糸からなる衣料用高嵩高厚地織編物の製造方法に関する。
【0002】
【従来の技術】
ポリエステル繊維は取り扱いやすく、適度の着用耐久性があり、さらに価格の面でも他の合成繊維に比べて有利であり衣料用繊維として極めて広い用途を有している。それらポリエステル繊維で作られた製品の中には、紡糸、延伸、加工、減量、染色等の工程において、様々な機能、風合いを与えたものが多く出ている。中でも、ソフトでふくらみを持った製品、従来の天然繊維にはなかった新しい風合いを持つ製品は消費者の側から多く望まれている。
【0003】
これらふくらみを持った製品を作る方法の一つとして、仮撚加工糸や収縮率の異なった原糸を混繊した異収縮混繊糸を用いる方法が知られている。仮撚加工糸は仮撚された状態で熱セットした後、解撚する事により得られる嵩高性に富んだ捲縮糸であるが、加工速度が遅いためにコストが高い、仮撚加工時に繊維断面が変形するためにくすんだ光沢になる、さらに糸構造的に均一であるために風合い的な特徴が出せない等の点から審美性に欠け高級用途への使用は不適当である。
【0004】
一方、異収縮混繊糸はポリエステル繊維の製造工程において紡糸、延伸条件の違いにより繊維の収縮率が変化することを利用したものであり、例えば別個に延伸熱セットした2種類のフィラメントを延伸機上または、延伸後に混繊することにより得られる。この混繊糸を製編織後に布帛状で熱処理することにより収縮差に応じた糸長差が発現し布帛にふくらみが生じる。
【0005】
しかしながら、この手法では収縮時の布帛拘束力が大きく十分な糸長差が出ないために目標とする風合いを得るには至っていない。そこで、さらに大きなふくらみ、ソフトさを得るための方法として、高収縮糸と加熱下で伸長する自己伸長糸を混繊する方法がある。
【0006】
自己伸長糸に関しては、ポリエチレンテレフタレートポリマーを紡糸、延伸して得られる糸を収縮処理する(特公昭41−1205号公報、特公昭43−28262号公報、特公平4−018051号公報)、あるいはポリエステル未延伸糸を収縮熱処理し、ついで延伸する(特公昭46−3372号公報、特公昭63−372号公報)、ポリエステル半延伸糸を弛緩熱処理する(特公平2−293410号公報)、ポリエステルマルチフィラメント部分配向未延伸糸を他のマルチフィラメントと混繊し次いで弛緩熱処理する(特開平6−299430号公報)などがあるが、いずれも従来の完成糸を製造する工程に加え、延伸、熱処理等の糸加工の手間がかかり経済面、作業面共に改善が望まれている。
【0007】
また、上記製造法において太繊度繊維を得ようとする場合、弛緩熱処理時のヒーター温度を高くするかあるいは加工速度を下げる必要があり生産性が低下するだけでなく、コストの面でも不利となり、さらに単糸間の熱処理ムラも大きくなるなど工業的に問題がある。
【0008】
【発明が解決しようとする課題】
本発明は上記従来技術の有する問題点を克服し、且つ従来の方法で製造することは困難とされた優れた風合い、ソフトでふくらみのある高嵩高厚地織編物をトータルデニールの大きいマルチフィラメントの高配向未延伸糸と延伸糸の混繊糸を用いて経済的かつ効率的に製造することを目的とする。
【0009】
【課題を解決するための手段】
本発明者らはポリエステル高配向未延伸糸をキャリヤー能を有する有機化合物を含む溶液で処理後、乾熱処理をすることにより自己伸長することを見出し、先に提案した。そして、上記目的を達成するためにさらなる鋭意検討を重ねた結果、この処理方法を用いると従来の方法では困難であったトータルデニールの大きい2種類の繊維群からなる混繊糸に十分な糸長差を付与でき、高嵩高性の布帛を経済的かつ効率的に得られることを見出し本発明に到達した。
【0010】
本発明におけるポリエステルとは繊維形成性のポリエステルであれば特に限定はされないが、例えばテレフタル酸、イソフタル酸、2,6−ナフタレンジカルボン酸を主たるカルボン酸成分とし、エチレングリコール、プロピレングリコールもしくはテトラメチレングリコールを主たるグリコール成分とするポリエチレンテレフタレート、ポリエチレンイソフタレート、ポリブチレンテレフタレート、あるいはポリエチレン2,6−ナフタレート等の線状ポリエステルを主成分としたものが好ましく、特にポリエチレンテレフタレートが好ましい。
【0011】
また、これらは用途によっては難燃性、易染性、制電性等の機能性の化合物が共重合或は混合していても、ダル剤、無機粒子及び種々の機能性微粒子等の添加剤が含まれていても構わない。
【0012】
本発明に用いるポリエステル繊維糸Aは上記の繊維形成性のポリエステルを例えば紡糸捲取速度2000から4500m/min.の範囲で溶融紡糸することにより得られ、ヤーンデニールが50以上150以下で、構造一体性パラメーターが0.1以上0.6以下、密度が1.36g/cm3 以下のものである。ここで言う構造一体性パラメーターとは湿熱80℃、0.2g/dの荷重下で30秒処理したときの伸長率であり、丸断面の時は複屈折(以後Δnとする)で代用しても構わない。その場合は、Δnは30×10-3〜60×10-3のものが好ましい。ここでのΔnは、ベレックコンペンセーターを装着した偏光顕微鏡によりレタデーションを測定し、レタデーションと繊維径により求められるものである。
【0013】
ヤーンデニールが50未満であると従来の方法を採用しても製造が可能となり、本発明の効果が活かせないだけでなく、混繊糸を構成する延伸糸の割合が増加しふくらみが不足する。また150以上であると混繊糸を構成する収縮糸の割合が減少し布帛の寸法安定性が悪くなる。
【0014】
構造一体性パラメーターが0.6を超えると配向性が不十分でキャリヤー処理時に結晶化が不十分であり、収縮が大きく自己伸長性が得られない。また、0.1未満であるとキャリヤー処理時に表層の結晶化が大きく同様に自己伸長性が得られない。従って、0.15〜0.4が好ましく、さらには0.2〜0.3がより好ましい。
【0015】
密度が1.36g/cm3 を超えると後加工での配向結晶化増加量が少なく自己伸長能が不十分となるから1.36g/cm3 以下が好ましく、更に好ましくは1.35g/cm3 以下である。
【0016】
本発明に用いるポリエステル繊維Bの沸水収縮率は12〜60%である。また、好ましくはヤーンデニールが30以上100以下、切断伸度が25以上40%以下、乾熱収縮応力の最大ピーク値が0.2g/d以上で最大ピーク温度が100℃以上のものである。
【0017】
ヤーンデニールが30未満であると、混繊糸を構成するポリエステル繊維糸Aの割合が増加し自己伸長後にポリエステル繊維糸Bに応力集中が生じ、着用時に変形しやすく寸法安定性を保つことができず実用性に欠ける。また、ヤーンデニールが100を超えると混繊糸を構成する自己伸長糸の割合が少なくなりふくらみ不足となり風合いが悪くなる。
【0018】
切断伸度が40%を超えると得られる布帛の寸法安定性が不良で実用性が低い。また、25%未満であると延伸操業性が低下し好ましくないうえ、製編織時の工程通過性を考慮すると切断伸度は25%以上とすることが望ましい。
【0019】
沸水収縮率が12%未満であると自己伸長糸との糸長差が不足して嵩高効果が不十分となり、60%を超える繊維は工業的に安定に製造することが難しい。また、乾熱収縮応力の最大ピーク値が0.2g/d未満であると、拘束力の大きい布帛中での収縮が不足し、糸長差が不十分となり嵩高性が十分出ない。更に好ましくは0.3g/d以上である。さらに、最大収縮応力のピーク温度が100℃未満であると、キャリヤー処理時に熱セットされ、収縮の発現が少なくなり、糸長差が小さく嵩高性に欠ける。更に好ましくは150℃以下である。
【0020】
本発明におけるポリエステル混繊糸は上記2種類の繊維群からなり、混繊糸を構成するポリエステル繊維糸Aとポリエステル繊維糸Bの構成比率はデニール比率で30:70から70:30であり、該混繊糸のトータルデニールは80以上250以下である。
【0021】
ポリエステル繊維糸Aの構成比率が30%未満すなわちポリエステル繊維糸Bの構成比率が70%を超えると、ふくらみが不十分であり風合いが悪くなる。また、繊維糸Aの構成比率が70%を超える、すなわち繊維糸Bの構成比率が30%未満であると、収縮糸である繊維糸Bに応力が集中し製編織工程の通過性が悪くなるだけでなく、布帛の寸法安定性も悪くなる。
【0022】
混繊糸のトータルデニールが80未満であると、従来技術で十分に対応でき本発明の効果が活かせない。また250を超えると衣料用途としての汎用性に乏しくなる。
【0023】
本発明におけるポリエステル繊維糸Aの断面形状は特に限定されないが、シルクライクな光沢発現あるいはドライな触感を期待する場合には三角断面が好ましい。一方、ポリエステル繊維糸Bに関しても断円形状は特に限定されないが、強度保持、紡糸操業性の観点から丸断面が好ましく、発色性効果を期待する場合には多葉断面を用いることもできる。
【0024】
本発明に用いられるポリエステル繊維糸Aの単糸デニールは0.5以上3dpf以下、延伸糸の単糸デニールは2以上5dpf以下が好ましい。
【0025】
ポリエステル繊維糸Aの単糸デニールが0.5dpf未満のものは製糸困難であり、3dpfを超えると風合い的にかたくなり実用性に欠ける。また、ポリエステル繊維糸Bの単糸デニールが2dpf未満であると強度保持としての役割が果たせず寸法変形しやすい。逆に5dpfを超えると布帛としてのソフトさに欠け実用性がなく、フィラメント数を極端に減らす必要がある。
【0026】
両者を混繊した後製編織するが、例えば糊付け工程やウオータージェットルームでの乾燥工程等の後述するキャリヤー処理工程に至るまでの工程で70℃を超える熱履歴を与えないことが重要であり、その理由はキャリヤー処理前に収縮応力を発現させないためである。
【0027】
本発明におけるポリエステルに対してキャリヤー能を有する有機化合物とは安息香酸、安息香酸エステル等の安息香酸誘導体、サリチル酸、サリチル酸エステル等のサリチル酸誘導体、フェノール、m−クレゾール等のフェノール類、モノクロロベンゼン、トリクロロベンゼン等のハロゲン化芳香族類、アセトフェノン等のケトン類、ハロゲン化フェノール類、フェニルフェノール類、アソニール等のエーテル類、ジ−およびトリフェニルメタン類、ジフェニル誘導体、メチルナフタレン、ナフトール等のナフタレン類、アニリン類等の主に芳香族系の有機化合物誘導体のいずれか1種又は2種以上の混合物をいう。
【0028】
これら、ポリエステルに対してキャリヤー能を有する有機化合物は、水系、有機溶剤系のいずれでも良い。また、ポリエステルに対してキャリヤー能を有する有機化合物以外に乳化剤、精練剤、分散剤、均染剤、PH緩衝剤等各種助剤および各種染料を場合によっては数種含んでいても良い。
【0029】
これらの処理は、処理自体単独で行うことも、精練工程、染色工程等と同時に行うこともでき、処理方法としては、精練浴と共に処理する、染色浴と共に処理する等の方法がある。また、単独で行う場合は本発明の処理方法以前にポリエステルのガラス転移点以上の温度がかからなければ、どの時点で行っても構わない。
【0030】
これらの処理はポリエステル繊維糸のガラス転移点以下で開始することが重要である。すなわち、ガラス転移点以上で処理を開始すると、処理液による収縮抑制機能が働く前に、原糸の収縮が生じ伸長しない。ゆえに、製品自体に欠点が多く発生し、風合いも硬くなり、ふくらみもでない。従って、キャリヤー能を有する0.5以上20%owf以下の濃度の有機化合物を含む溶液中で、ガラス転移点以下の温度で処理を開始し最終到達温度が70℃以上100℃以下になるようにして収縮を抑制し、その後の工程にて乾熱120℃以上190℃以下で処理することにより自発伸長を発現させる。
【0031】
処理工程の作業性、コストからは、開始温度はガラス転移点以下でできるだけ高い方が望ましく、処理時間も短くすることができる。有機化合物の濃度に関しても、高い方が望ましいが、20%owfを超えると溶液との相溶性、安全性、処理液コスト等に問題が生じてくる。逆に0.5%owf未満であると収縮抑制の効果が小さく、後の乾熱処理時の伸長性が低下する。好ましくは4以上15%owf以下である。
【0032】
キャリヤー処理最終温度が100℃を超えると、高圧処理釜が必要でコストが高くなり、70℃未満であると結晶化による低収縮化不十分で乾熱処理時の伸長性が低下する。
【0033】
上記の方法で伸長処理された製品は伸長した時点で安定であり、その後の精練、セット、減量、染色、加工等の工程ではなんら問題を生じない。
【0034】
以下、実施例により本発明を説明する。
【実施例】
以下実施例により本発明を説明する。
尚、本発明の評価に用いた測定方法以下の通りである。
〔沸水収縮率(SHW)〕
d(デニール)×1/30gに相当する荷重を加え、原糸50.0cmの長さにあらかじめ印を付けておきガーゼに包んだ後、沸水中に30分間浸漬し、風乾した後同荷重を加えて印の間の長さ(L)を測定し、以下の式で算出した。
SHW(%)=100×(50−L)/50
〔乾熱収縮応力の最大ピーク値と最大ピーク温度〕
0.05g/dの初荷重を加え、室温から300℃まで20℃/分の昇温速度で昇温した時の収縮応力の変化を測定し、その最大ピーク値と最大ピーク温度を各々の値とした。
〔密度〕
n−ヘプタンと四塩化炭素からなる密度勾配管を用いて30℃で測定した。
(実施例1〜7、比較例1〜7)
ポリエチレンテレフタレートを常法により紡速2000から4500m/min.で溶融紡糸して得た丸断面または三角断面の高配向未延伸糸と、紡速1300〜3000m/min.で紡糸し、延伸して得た延伸糸を試料I〜VIIIおよび試料i〜vi、IXとしてそれぞれ得た(表1および表2)。これらの糸を交絡ノズルを用いて流体交絡混繊を行い、得られた混繊糸に1200回/mのS撚を付与して70℃で熱セットし、これを経糸及び緯糸として用い、これらを2本交互に打ち込んだ平組織の織物をなし、得られた織物に処理を施した。処理方法は以下に示す。
【0035】
織物サンプル5.0gをオルト−フェニルフェノール系のキャリヤーであるテトロシンOEN(山川薬品(株))が2g/lの濃度(キャリヤー濃度10%owf相当、有機物質濃度約6.0%owf相当)に分散し、調整されたエマルジョンの処理液250mlに入れ(浴比1:50)、ミニカラー染色機にて処理温度30℃で開始し、撹拌しながら1℃/min.の速度で昇温していき、浴温度を80℃まで昇温した後、20分撹拌を行い、冷却して取り出した。処理後、洗浄および乾燥を行い製品を得た。得られた製品はポリエステル織物の風合い評価の経験の長い染色加工技術者3名によってソフトさ、ふくらみ程度、風合いの新規性を判定した。その結果を表3に示す。
【0036】
実施例1〜7はいずれも従来にないソフトさふくらみを有しており、風合い的に優れたものであった。中でも実施例1〜3及び6、7は非常に嵩高性に富み、優れた風合いを有していた。また、キャリヤー濃度を1%owfとした以外は実施例1と全く同条件で処理した場合、およびキャリヤー濃度を18%owfとした以外は実施例1と全く同条件で処理時した場合共に風合い的には実施例1で得られた織物には劣るものの十分な嵩高性を有していた。
【0037】
比較例1、2および6〜9はソフトさふくらみ共に欠け風合い的に良いものではなかった。また、比較例3は風合い的には良いものの寸法変化し易く実用的に欠けるものであった。比較例4は風合い的には良いが、糸が太過ぎるため汎用性に欠ける。比較例5は風合い的には優れているものの、目的とする厚地織物が得られない。
【0038】
また、処理時に浴中にサンプルに使用した各高配向未延伸糸及び延伸糸を入れ、伸長率及び収縮率を以下の方法で測定した。d(デニール)×1/30gに相当する荷重を加え、原糸50.0cmの長さにあらかじめ印を付けておきガーゼに包んだ後、織物サンプルと一緒にキャリヤー能を有する処理液中に入れ、処理後風乾した後、引き続き160℃のオーブンで30分間処理し、処理後に同荷重を加えて印の間の長さ(W)を測定した。それぞれの値は以下の式で算出した。
伸長率(%)=100×(W−50)/50
収縮率(%)=100×(50−W)/50
この結果も表3に示す。
【0039】
(比較例8、9)
高配向未延伸糸IIと延伸糸iの混繊糸を用い、処理温度を下記条件とする以外は実施例1〜7と同じ条件にて処理し、その後冷却して取り出した。
110℃まで昇温した後、110℃で20分撹拌(比較例8)
50℃まで昇温した後、50℃で20分撹拌(比較例9)
【0040】
【表1】

Figure 0003666616
【0041】
【表2】
Figure 0003666616
【0042】
【表3】
Figure 0003666616
【0043】
【発明の効果】
本発明におけるトータルデニールの大きい2種類の繊維群からなるポリエステル混繊糸を用いた厚地織編物へのキャリヤー能を有する有機化合物での処理は、一方のポリエステル繊維群の収縮能を抑制すると共に、自己伸長性を与える作用効果がある。そこで、かかるポリエステル混繊糸布帛にこの処理を行うことにより、従来行っていたポリエステル高配向未延伸糸への、延撚、延伸仮撚、弛緩熱処理等の工程を削減できるだけでなく、ソフトでふくらみのある独特の風合いを有した製品を低コストでかつ効率的に製造することが可能となる。[0001]
BACKGROUND OF THE INVENTION
TECHNICAL FIELD The present invention relates to a method for producing a soft and swelled bulky thick woven fabric having an excellent texture, and more specifically, a method for producing a high bulky thick woven fabric for clothing comprising a blended yarn of self-stretching yarn and shrinking yarn. About.
[0002]
[Prior art]
Polyester fibers are easy to handle, have moderate wear durability, and are advantageous over other synthetic fibers in terms of price, and have a very wide range of uses as clothing fibers. Many products made of these polyester fibers have been given various functions and textures in processes such as spinning, drawing, processing, weight loss, and dyeing. Among them, many products are desired from the consumer side that are soft and swelled, and products that have a new texture not found in conventional natural fibers.
[0003]
As a method for producing a product having such a bulge, there is known a method using false twisted yarn or different shrinkage mixed yarn obtained by mixing raw yarns having different shrinkage rates. False twisted yarn is a crimped yarn with high bulkiness that is obtained by untwisting after heat setting in the false twisted state, but the cost is high due to slow processing speed. It is unsuitable for use in high-grade applications because it has a dull luster due to the deformation of the cross section and lacks aesthetics because it is uniform in the yarn structure and cannot produce a textured characteristic.
[0004]
On the other hand, different shrinkage blended yarns utilize the fact that the shrinkage rate of the fibers changes depending on the spinning and drawing conditions in the polyester fiber manufacturing process. For example, two types of filaments that have been separately drawn and heat set are drawn into a drawing machine. It can be obtained by blending up or after stretching. When this mixed yarn is heat-treated in the form of a fabric after weaving and weaving, a yarn length difference corresponding to the difference in shrinkage is developed, and the fabric is swelled.
[0005]
However, in this method, since the fabric restraining force at the time of contraction is large and a sufficient yarn length difference does not occur, a target texture has not been obtained. Therefore, as a method for obtaining a larger swell and softness, there is a method of blending a high shrinkage yarn and a self-extension yarn that elongates under heating.
[0006]
Regarding the self-elongating yarn, a yarn obtained by spinning and drawing a polyethylene terephthalate polymer is subjected to shrinkage treatment (Japanese Patent Publication No. 41-1205, Japanese Patent Publication No. 43-28262, Japanese Patent Publication No. 4-018051), or polyester. An undrawn yarn is subjected to shrink heat treatment and then drawn (Japanese Examined Patent Publication No. 46-3372 and Japanese Examined Patent Publication No. 63-372), and a polyester semi-drawn yarn is subjected to relaxation heat treatment (Japanese Examined Patent Publication No. 2-293410). The partially oriented undrawn yarn is mixed with other multifilaments and then subjected to relaxation heat treatment (Japanese Patent Laid-Open No. Hei 6-299430). It takes time and effort for yarn processing, and improvements in both economic and work aspects are desired.
[0007]
Also, when trying to obtain a thick fiber in the above production method, it is necessary to increase the heater temperature during the relaxation heat treatment or lower the processing speed, not only productivity is lowered, but also in terms of cost, Further, there are industrial problems such as uneven heat treatment between single yarns.
[0008]
[Problems to be solved by the invention]
The present invention overcomes the above-mentioned problems of the prior art, and has an excellent texture, soft and swelled high bulky thick fabric knitted fabric that is difficult to manufacture by the conventional method. An object is to economically and efficiently produce a blended yarn of oriented undrawn yarn and drawn yarn.
[0009]
[Means for Solving the Problems]
The present inventors have found that the polyester highly oriented undrawn yarn is self-stretched by treating it with a solution containing an organic compound having a carrier ability and then subjecting it to a dry heat treatment. As a result of further earnest studies to achieve the above object, a yarn length sufficient for a blended yarn composed of two types of fiber groups having a large total denier, which was difficult with the conventional method when this processing method was used. The present inventors have found that a difference can be imparted and a highly bulky fabric can be obtained economically and efficiently.
[0010]
The polyester in the present invention is not particularly limited as long as it is a fiber-forming polyester. For example, terephthalic acid, isophthalic acid, 2,6-naphthalenedicarboxylic acid is the main carboxylic acid component, and ethylene glycol, propylene glycol or tetramethylene glycol. The main component is linear terephthalate such as polyethylene terephthalate, polyethylene isophthalate, polybutylene terephthalate, or polyethylene 2,6-naphthalate having a main glycol component, and polyethylene terephthalate is particularly preferable.
[0011]
In addition, depending on the use, additives such as dull agents, inorganic particles and various functional fine particles may be used even if functional compounds such as flame retardant, dyeability, and antistatic properties are copolymerized or mixed. May be included.
[0012]
For the polyester fiber yarn A used in the present invention, the above fiber-forming polyester is used, for example, at a spinning take-up speed of 2000 to 4500 m / min. The yarn denier is 50 to 150, the structural integrity parameter is 0.1 to 0.6, and the density is 1.36 g / cm 3 or less. The structural integrity parameter here refers to the elongation when treated for 30 seconds under a load of 80 ° C. and a load of 0.2 g / d. In the case of a round cross section, birefringence (hereinafter referred to as Δn) is substituted. It doesn't matter. In that case, Δn is preferably 30 × 10 −3 to 60 × 10 −3 . Here, Δn is obtained by measuring the retardation with a polarizing microscope equipped with a Berek compensator and calculating the retardation and fiber diameter.
[0013]
When the yarn denier is less than 50, the production is possible even if the conventional method is adopted, and not only the effect of the present invention cannot be utilized, but also the ratio of the drawn yarn constituting the mixed yarn is increased and the swelling is insufficient. On the other hand, if it is 150 or more, the ratio of the shrink yarn constituting the mixed yarn is reduced, and the dimensional stability of the fabric is deteriorated.
[0014]
When the structural integrity parameter exceeds 0.6, the orientation is insufficient and crystallization is insufficient during the carrier treatment, resulting in large shrinkage and no self-extension. On the other hand, if it is less than 0.1, the surface layer is greatly crystallized during the carrier treatment, and self-stretchability cannot be obtained. Therefore, 0.15-0.4 is preferable, and 0.2-0.3 is more preferable.
[0015]
When the density exceeds 1.36 g / cm 3 , the amount of increase in orientation crystallization in post-processing is small and the self-extension ability is insufficient, so 1.36 g / cm 3 or less is preferable, and more preferably 1.35 g / cm 3. It is as follows.
[0016]
The boiling water shrinkage of the polyester fiber B used in the present invention is 12 to 60%. Preferably, the yarn denier is 30 to 100, the elongation at break is 25 to 40%, the maximum peak value of dry heat shrinkage stress is 0.2 g / d or more, and the maximum peak temperature is 100 ° C. or more.
[0017]
If the yarn denier is less than 30, the proportion of the polyester fiber yarn A constituting the mixed yarn increases, stress concentration occurs in the polyester fiber yarn B after self-elongation, and it is easy to be deformed when worn and can maintain dimensional stability. It lacks practicality. On the other hand, when the yarn denier exceeds 100, the ratio of the self-stretching yarn constituting the blended yarn is decreased, resulting in insufficient swelling and poor texture.
[0018]
If the cut elongation exceeds 40%, the resulting fabric has poor dimensional stability and low utility. Further, if it is less than 25%, the stretching operability is lowered, which is not preferable, and the cut elongation is preferably 25% or more in consideration of process passability during weaving and weaving.
[0019]
If the boiling water shrinkage is less than 12%, the yarn length difference from the self-stretching yarn is insufficient and the bulkiness effect becomes insufficient, and fibers exceeding 60% are difficult to produce industrially stably. Further, when the maximum peak value of the dry heat shrinkage stress is less than 0.2 g / d, the shrinkage in the fabric having a large restraining force is insufficient, the yarn length difference is insufficient, and the bulkiness is not sufficiently obtained. More preferably, it is 0.3 g / d or more. Further, when the peak temperature of the maximum shrinkage stress is less than 100 ° C., heat setting is performed during the carrier treatment, shrinkage is reduced, the yarn length difference is small, and the bulkiness is lacking. More preferably, it is 150 degrees C or less.
[0020]
The polyester blended yarn in the present invention is composed of the above two types of fiber groups, and the composition ratio of the polyester fiber yarn A and the polyester fiber yarn B constituting the blended yarn is 30:70 to 70:30 in terms of denier, The total denier of the blended yarn is 80 or more and 250 or less.
[0021]
When the constituent ratio of the polyester fiber yarn A is less than 30%, that is, the constituent ratio of the polyester fiber yarn B exceeds 70%, the bulge is insufficient and the texture becomes poor. Further, if the constituent ratio of the fiber yarn A exceeds 70%, that is, if the constituent ratio of the fiber yarn B is less than 30%, stress concentrates on the fiber yarn B that is a shrink yarn, and the passability in the weaving and knitting process deteriorates. In addition, the dimensional stability of the fabric also deteriorates.
[0022]
If the total denier of the blended yarn is less than 80, the conventional technique can sufficiently cope with the effect of the present invention. On the other hand, if it exceeds 250, the versatility for apparel will be poor.
[0023]
The cross-sectional shape of the polyester fiber yarn A in the present invention is not particularly limited, but a triangular cross-section is preferable when a silky gloss expression or a dry tactile sensation is expected. On the other hand, the round shape of the polyester fiber yarn B is not particularly limited, but a round cross section is preferable from the viewpoint of strength retention and spinning operability, and a multi-leaf cross section can be used when a coloring effect is expected.
[0024]
The single yarn denier of the polyester fiber yarn A used in the present invention is preferably 0.5 to 3 dpf, and the single yarn denier of the drawn yarn is preferably 2 to 5 dpf.
[0025]
Polyester fiber yarn A having a single yarn denier of less than 0.5 dpf is difficult to produce yarn, and if it exceeds 3 dpf, it feels harder and lacks practicality. Further, if the single yarn denier of the polyester fiber yarn B is less than 2 dpf, the polyester fiber yarn B does not serve as strength maintenance and is likely to undergo dimensional deformation. Conversely, if it exceeds 5 dpf, the softness of the fabric is lacking and there is no practicality, and the number of filaments must be extremely reduced.
[0026]
It is important not to give a heat history exceeding 70 ° C. in the process up to the carrier treatment process described later, such as a gluing process or a drying process in a water jet loom, for example, after knitting and weaving both. The reason is that shrinkage stress is not developed before the carrier treatment.
[0027]
The organic compound having carrier ability with respect to the polyester in the present invention includes benzoic acid derivatives such as benzoic acid and benzoic acid esters, salicylic acid derivatives such as salicylic acid and salicylic acid esters, phenols such as phenol and m-cresol, monochlorobenzene, triphenyl. Halogenated aromatics such as chlorobenzene, ketones such as acetophenone, halogenated phenols, phenylphenols, ethers such as asynol, di- and triphenylmethanes, diphenyl derivatives, naphthalenes such as methylnaphthalene and naphthol, It means any one kind or a mixture of two or more kinds of mainly aromatic organic compound derivatives such as anilines.
[0028]
These organic compounds having carrier ability with respect to polyester may be either water-based or organic solvent-based. Further, in addition to the organic compound having carrier ability with respect to the polyester, various kinds of auxiliary agents such as emulsifiers, scouring agents, dispersants, leveling agents, pH buffering agents, and various dyes may be included in some cases.
[0029]
These treatments can be performed alone or simultaneously with the scouring step, the dyeing step, and the like. The treatment method includes a treatment with a scouring bath and a treatment with a dyeing bath. Moreover, when performing independently, as long as the temperature beyond the glass transition point of polyester is not applied before the processing method of this invention, you may carry out at any time.
[0030]
It is important that these treatments start below the glass transition point of the polyester fiber yarn. That is, when the treatment is started at the glass transition point or higher, the raw yarn shrinks and does not elongate before the shrinkage suppressing function by the treatment liquid works. Therefore, many defects occur in the product itself, the texture becomes hard, and there is no swelling. Therefore, the treatment is started at a temperature not higher than the glass transition point in a solution containing an organic compound having a carrier ability and having a concentration of not less than 0.5 and not more than 20% owf so that the final temperature reaches not less than 70 ° C. and not more than 100 ° C. The shrinkage is suppressed, and spontaneous elongation is caused to develop by treatment at a dry heat of 120 ° C. or higher and 190 ° C. or lower in the subsequent steps.
[0031]
From the workability and cost of the treatment process, it is desirable that the starting temperature is as high as possible below the glass transition point, and the treatment time can be shortened. A higher concentration of the organic compound is also desirable, but if it exceeds 20% owf, problems arise in compatibility with the solution, safety, cost of the processing solution, and the like. Conversely, if it is less than 0.5% owf, the effect of suppressing shrinkage is small, and the extensibility during the subsequent dry heat treatment is lowered. Preferably, it is 4 or more and 15% owf or less.
[0032]
If the final carrier treatment temperature exceeds 100 ° C, a high-pressure treatment kettle is required and the cost is high, and if it is less than 70 ° C, low shrinkage due to crystallization is insufficient and the extensibility during dry heat treatment is lowered.
[0033]
The product stretched by the above method is stable when stretched, and does not cause any problems in the subsequent steps such as scouring, setting, weight loss, dyeing, and processing.
[0034]
Hereinafter, the present invention will be described by way of examples.
【Example】
The following examples illustrate the invention.
The measurement method used for the evaluation of the present invention is as follows.
[Boiling water shrinkage (SHW)]
Apply a load corresponding to d (denier) x 1/30 g, mark the length of the original yarn 50.0 cm in advance, wrap it in gauze, immerse it in boiling water for 30 minutes, air-dry and then apply the same load. In addition, the length (L) between the marks was measured and calculated by the following formula.
SHW (%) = 100 × (50−L) / 50
[Maximum peak value and maximum peak temperature of dry heat shrinkage stress]
The initial load of 0.05 g / d was applied, and the change in shrinkage stress when the temperature was increased from room temperature to 300 ° C. at a rate of temperature increase of 20 ° C./min was measured. It was.
〔density〕
It measured at 30 degreeC using the density gradient tube which consists of n-heptane and carbon tetrachloride.
(Examples 1-7, Comparative Examples 1-7)
Polyethylene terephthalate was spun at a spinning speed of 2000 to 4500 m / min. A highly oriented undrawn yarn having a round or triangular cross section obtained by melt spinning at a spinning speed of 1300 to 3000 m / min. The drawn yarns obtained by spinning and drawing were obtained as Samples I to VIII, Samples i to vi, and IX, respectively (Tables 1 and 2). These yarns are subjected to fluid entanglement using a entanglement nozzle, S twist of 1200 times / m is applied to the obtained mixed yarn and heat-set at 70 ° C., and this is used as warp and weft. A fabric having a plain structure in which two yarns were alternately driven was formed, and the resulting fabric was treated. The processing method is shown below.
[0035]
Tetrocin OEN (Yamakawa Yakuhin Co., Ltd.), an ortho-phenylphenol carrier, has a concentration of 2 g / l (equivalent to a carrier concentration of 10% owf, equivalent to an organic substance concentration of about 6.0% owf). Dispersed and prepared in 250 ml of the prepared emulsion treatment solution (bath ratio 1:50), started at a treatment temperature of 30 ° C. in a mini-color dyeing machine, and stirred at 1 ° C./min. The bath temperature was raised to 80 ° C., stirred for 20 minutes, cooled and taken out. After the treatment, washing and drying were performed to obtain a product. The obtained product was judged for softness, bulge degree and novelty of texture by three dyeing engineers with long experience in texture evaluation of polyester fabrics. The results are shown in Table 3.
[0036]
Each of Examples 1 to 7 had a soft swell that was not found in the past, and was excellent in texture. Among them, Examples 1 to 3, 6, and 7 were very bulky and had an excellent texture. In addition, when the treatment is performed under exactly the same conditions as in Example 1 except that the carrier concentration is 1% owf, and when the treatment is performed under exactly the same conditions as in Example 1 except that the carrier concentration is 18% owf, both are textured. Although it was inferior to the woven fabric obtained in Example 1, it had sufficient bulkiness.
[0037]
In Comparative Examples 1, 2 and 6-9, neither soft bulge nor good texture was found. Moreover, although the comparative example 3 was good in texture, it was easy to change in dimensions and was practically lacking. Comparative Example 4 is good in texture, but lacks versatility because the yarn is too thick. Although the comparative example 5 is excellent in texture, the intended thick fabric is not obtained.
[0038]
Moreover, each highly oriented unstretched yarn and stretched yarn used for the sample were put in the bath at the time of processing, and the elongation and shrinkage were measured by the following methods. Apply a load equivalent to d (denier) x 1/30 g, mark the length of the original yarn 50.0 cm in advance and wrap it in gauze, then put it in a treatment solution with carrier ability together with the fabric sample After the treatment, it was air-dried, and subsequently treated in an oven at 160 ° C. for 30 minutes. After the treatment, the same load was applied to measure the length (W) between the marks. Each value was calculated by the following formula.
Elongation rate (%) = 100 × (W−50) / 50
Shrinkage rate (%) = 100 × (50−W) / 50
The results are also shown in Table 3.
[0039]
(Comparative Examples 8 and 9)
A mixed yarn of highly oriented undrawn yarn II and drawn yarn i was used, and the treatment temperature was the same as in Examples 1 to 7 except that the following conditions were satisfied. Thereafter, the yarn was cooled and taken out.
After heating up to 110 ° C., the mixture was stirred at 110 ° C. for 20 minutes (Comparative Example 8).
After heating up to 50 ° C., the mixture was stirred at 50 ° C. for 20 minutes (Comparative Example 9).
[0040]
[Table 1]
Figure 0003666616
[0041]
[Table 2]
Figure 0003666616
[0042]
[Table 3]
Figure 0003666616
[0043]
【The invention's effect】
In the present invention, the treatment with the organic compound having a carrier ability to the thick ground knitted fabric using the polyester mixed yarn composed of two kinds of fiber groups having a large total denier suppresses the shrinkage ability of one polyester fiber group, Has the effect of giving self-extension. Therefore, by performing this treatment on such a polyester blended fiber fabric, not only can the conventional steps such as drawing, drawing false twisting, relaxation heat treatment, etc., be performed on the polyester highly oriented undrawn yarn, but also soft and bulge. It is possible to efficiently produce a product having a certain unique texture at a low cost.

Claims (7)

ヤーンデニールが50〜150で構造一体性パラメーターが0.1〜0.6のポリエステル繊維糸Aと、沸水収縮率が12〜60%のポリエステル繊維糸Bとからなる混繊糸を用いて製編織し、次いでキャリヤー能を有する有機化合物を含む溶液中で最終到達温度を70〜100℃となる条件で処理し、その後120〜190℃で乾熱処理することを特徴とする厚地織編物の製造方法。 Knitting and weaving using a blended yarn composed of a polyester fiber yarn A having a yarn denier of 50 to 150 and a structural integrity parameter of 0.1 to 0.6 and a polyester fiber yarn B having a boiling water shrinkage of 12 to 60% Next, a method for producing a thick knitted fabric knitted fabric, which is treated in a solution containing an organic compound having a carrier ability under a condition that the final temperature reaches 70 to 100 ° C., followed by a dry heat treatment at 120 to 190 ° C. 混繊後の工程で70℃を超える工程を経由することなくキャリヤー処理工程に供することを特徴とする請求項1記載の厚地織編物の製造方法。 The method for producing a thick woven or knitted fabric according to claim 1, wherein the method is subjected to a carrier treatment step without passing through a step exceeding 70 ° C in the step after blending. キャリヤー能を有する有機化合物が0.5〜20%owfの濃度で溶液中に含有されてなることを特徴とする請求項1又は2記載の厚地織編物の製造方法。 3. The method for producing a thick woven or knitted fabric according to claim 1, wherein the organic compound having carrier ability is contained in the solution at a concentration of 0.5 to 20% owf. ポリエステル繊維糸Aの密度が1.36g/cm 3 以下の高配向未延伸糸であることを特徴とする請求項1〜3のいずれかに記載の厚地織編物の製造方法。The density of the polyester fiber yarn A is 1.36 g / cm 3 The method for producing a thick woven or knitted fabric according to any one of claims 1 to 3, wherein the yarn is the following highly oriented undrawn yarn. ポリエステル繊維糸Bのヤーンデニールが30〜100で、切断伸度が25〜40%、乾熱収縮応力の最大ピーク値が0.2g/d以上で最大ピーク温度が100℃以上の延伸糸であることを特徴とする請求項1〜4のいずれかに記載の厚地織編物の製造方法。 Polyester fiber yarn B is a drawn yarn having a yarn denier of 30 to 100, a cut elongation of 25 to 40%, a maximum peak value of dry heat shrinkage stress of 0.2 g / d or more and a maximum peak temperature of 100 ° C. or more. The method for producing a thick woven or knitted fabric according to any one of claims 1 to 4. 混繊糸を構成するポリエステル繊維糸Aとポリエステル繊維糸Bの構成比率がデニール比で30:70〜70:30であることを特徴とする請求項1〜5のいずれかに記載の厚地織編物の製造方法。 The thick woven or knitted fabric according to any one of claims 1 to 5, wherein the polyester fiber yarn A and the polyester fiber yarn B constituting the blended yarn have a denier ratio of 30:70 to 70:30. Manufacturing method. キャリヤー能を有する有機化合物を含む溶液処理をポリエステル繊維糸Aのガラス転移点温度以下で処理を開始することを特徴とする請求項1〜6のいずれかに記載の厚地織編物の製造方法。The method for producing a thick woven or knitted fabric according to any one of claims 1 to 6, wherein the solution treatment containing an organic compound having a carrier ability is started at a temperature equal to or lower than the glass transition temperature of the polyester fiber yarn A.
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