JPS6347803B2 - - Google Patents
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- Publication number
- JPS6347803B2 JPS6347803B2 JP56082535A JP8253581A JPS6347803B2 JP S6347803 B2 JPS6347803 B2 JP S6347803B2 JP 56082535 A JP56082535 A JP 56082535A JP 8253581 A JP8253581 A JP 8253581A JP S6347803 B2 JPS6347803 B2 JP S6347803B2
- Authority
- JP
- Japan
- Prior art keywords
- thick
- yarn
- thin
- roller
- temperature
- 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
Links
- 238000010438 heat treatment Methods 0.000 claims description 20
- 229920000728 polyester Polymers 0.000 claims description 18
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 230000007704 transition Effects 0.000 claims description 5
- 238000004804 winding Methods 0.000 claims description 4
- 239000008186 active pharmaceutical agent Substances 0.000 claims 2
- 238000000034 method Methods 0.000 description 15
- 239000004744 fabric Substances 0.000 description 13
- 238000009987 spinning Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- -1 polyethylene terephthalate Polymers 0.000 description 8
- 238000009835 boiling Methods 0.000 description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 6
- 239000005020 polyethylene terephthalate Substances 0.000 description 6
- 230000007423 decrease Effects 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 239000003513 alkali Substances 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- CARJPEPCULYFFP-UHFFFAOYSA-N 5-Sulfo-1,3-benzenedicarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(S(O)(=O)=O)=C1 CARJPEPCULYFFP-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Description
本発明はポリエステルよりなるシツクアンドシ
ンヤーンの製造方法に関する。
ポリエステルシツクアンドシンヤーン、即ち繊
度が変化する単糸よりなるポリエステルヤーン
は、それによつて得られる布帛が特異な風合を呈
し、またこの布帛を染色すると霜降り状を呈する
ことから、特殊なヤーンとして知られている。
従来より、ポリエステルシツクアンドシンヤー
ンの製造方法として、ポリエステルヤーンの紡糸
中又は延伸中に、溝付ローラ又はガイドとの接触
角を変化させてヤーン張力を変動させる方法、2
成分よりなる複合繊維を紡糸する際に2成分の吐
出割合を変化させる方法等が知られている。しか
しながら、かかる方法では装置が複雑になり、し
かも生産性が悪いため工業的には実施されない。
また、ポリエステル未延伸糸を適当な倍率と温
度で延伸することによつてシツクアンドシンヤー
ンとする方法も知られている。しかしながら、こ
の方法によると、シツクアンドシンのパターン
は、使用する未延伸糸の経時変化によつて大きく
変動する。更に、この方法では、使用する未延伸
糸パツケージの内外層によつても、シツクアンド
シンのパターンが大きく変動する。従つて、この
方法では、所定のシツクアンドシンのパターンを
有するヤーンを安定して製造することはできず、
工業的に採用できない。
本発明者らは、特別な装置を使用せず、生産性
よく、所定のシツクアンドシンヤーンを安定して
製造する方法について鋭意検討の結果、ポリエス
テルを溶融紡糸し、一旦捲取ることなく特定の条
件で引取り、続いて特定の条件で延伸すれば、上
記目的を達成できることを知り、先に提案した。
しかしながら、この方法で得られたシツクアンド
シンヤーンを仮撚加工、撚糸加工に付すと、断
糸、毛羽が生じ易く、更にアルカリ減量加工を施
すとシツク部の強力が低下し摩擦堅牢度が悪化す
るという問題が起つてくる。
また、寸法安定性が悪く熱収縮率が大きい(沸
水収縮率で10%以上)ため、布帛にした後の熱処
理によつて、布帛の風合が硬くなつてしまうとい
う欠点もある。そこで、本発明者らは、これらの
問題点を解決すべく、更に検討を重ねた結果、特
定条件下で紡糸、延伸した後、特定の条件下で熱
処理すればよいことを見出し、本発明に到達し
た。
即ち、本発明はポリエステルを溶融吐出して
3500m/分以下の速度で引取り、引続いて一旦巻
取ることなくポリエステルの二次転移点以下の温
度及び下記式
167/S.S.+1.21≦D.R.≦2100/S.S.+1.12
〔式中、S.S.は引取速度(m/分)、D.R.は延伸
倍率(倍)である。〕
を満足する倍率で延伸し、更に弛緩状態にて140
〜180℃の温度で熱処理してから巻取ることを特
徴とするシツクアンドシンヤーンの製造方法であ
る。
本発明で言うポリエステルとはポリエチレンテ
レフタレートを主たる対策とするが、テレフタル
酸成分の一部(通常15モル%以下)を他の二塩基
酸成分、例えばイソフタル酸、5−スルホイソフ
タル酸、アジピン酸等で置き換えてもよく、エチ
レングリコール成分の一部又は全部を炭素数3〜
10のアルキレングリコール、特にブチレングリコ
ールで置き換えても、また一部であればポリオキ
シエチレングリコールの如きポリオキシアルキレ
ングリコールで置き換えてもよい。かかるポリエ
ステルの重合度は、ポリエステルの種類、製品の
シツクアンドシンヤーンの用途に応じて適宜選定
すべきである。通常ポリエチレンテレフタレート
の場合、35℃のo−クロロフエノール溶液で測定
した値より求めた極限粘度〔η〕にして0.55〜
0.7のものが好ましい。
上記ポリエステルを溶融押出しするに際して
は、特別の手段を採用する必要はなく、任意の方
法が採用され、紡糸に引続いて延伸するに当つて
も、任意の直延方式が採用されるが、通常、紡糸
口金下に給油ローラ、流体噴射ノズル、引取ロー
ラと予熱供給ローラを兼ねたローラを順に設け、
このローラの下流に段付加熱延伸ローラを設置し
た装置が設備的にコンパクトで製造上有利であ
る。
第1図は、好ましい直延方式の一例を示す概略
図であり、図中1は紡糸装置、Yは紡出ヤーン、
2はオイリングローラ、3は流体噴射ノズル、4
は予熱ローラを兼ねた引取ローラ、5はセパレー
トローラ、6は段付加熱延伸ローラ、7は交絡処
理ノズル、8はワインダーである。
紡糸装置1より紡出されたヤーンYは、オイリ
ングローラ2により油剤を付与され、流体噴射ノ
ズル3によつて交絡処理された後、延伸温度に予
熱した引取ローラ4にセパレートローラ5を介し
て数回巻かれて所定速度で引取られると同時に延
伸温度に予熱され、下流の段付加熱延伸ローラ6
により所定倍率に延伸され、ひきつづき、所定温
度に加熱された段付加熱延伸ローラ6に数回巻か
れて、該延伸ローラ6の大径部6aと小径部6b
との周速の基に基づく弛緩率の下で熱処理され、
次いで必要に応じて交絡処理ノズル7によつて交
絡を付与されワインダー8に捲取られる。
この際、流体噴射ノズル3によつて付与される
交絡数は、5〜40個/mの範囲が好ましい。ま
た、この交絡数を調整することによつてシツクア
ンドシンのパターンを制御することもできる。な
お、ここで言う交絡数は、流動パラフインを浮か
せた水にヤーンを入れて測定した未開繊個数であ
る。
また、引取速度即ち引取ローラ4の表面速度は
3500m/分以下にする必要がある。この引取速度
を3500m/分より速くすると、得られるヤーンの
シツク部とシン部のコントラストが不充分にな
る。この引取速度をあまりに遅くすると、生産性
が低下するので1000m/分以上が好ましい。
上記引取ローラ4の予熱温度即ち延伸温度は、
使用するポリエステルの二次転移点以下にすべき
である。二次転移点より高くすると、シツクアン
ドシンのコントラストが小さくなり且つシツクア
ンドシンの発生も不安定になる。また、この温度
をあまりに低くすると、この温度が雰囲気温度に
よつて変動し易くなり、そのためシツクアンドシ
ンの発生が不安定になるので、常温(通常25℃)
以上にするのが好ましい。
延伸倍率は、あまりに低いと、シツク部とシン
部が長くなつて充分なシツクアンドシンが発現し
難くなる。延伸倍率を高くすれば、シツクアンド
シンが発現するが、あまり高くすると、シツク部
とシン部の差が小さくなる。本発明者の数多くの
実験の結果、適正な延伸倍率は前記式を満足しな
ければならないことを究明した。即ち、適正な延
伸倍率D.R.(倍)は、引取速度によつて相違し、
引取速度をS.S.(m/分)とすれば下記式
167/S.S.+1.21≦D.R.≦2100/S.S.+1.12
を満足させる必要がある。この引取速度S.S.
(m/分)に対する適正延伸倍率の範囲を図示し
たものが第2図である。
尚、本発明においては、紡糸した糸条を一旦巻
取ることなく、連続して延伸することが必要で、
紡糸工程で一旦巻取つた後延伸すると、末延伸糸
の経時によつて、シツクアンドシンの形態に変化
が生じ、一定形態のシツクアンドシンヤーンを安
定に製造することができない。
かくして得られるシツクアンドシンヤーンに
は、弛緩状態下で140〜180℃の温度にて熱処理を
施す。この弛緩率は、特に限定されないが、5%
以下が常用され、特に1〜4%が好ましい。弛緩
率を大きくしすぎるとシツク部の配向が乱れて脆
化現象が起る傾向がみられ、更に延伸、熱処理装
置上でヤーンがたるんで、安定した状態で延伸、
熱処理が行なえなくなる傾向がみられる。伸長又
は定長での熱処理では、シツク部の細化が起り、
シツクアンドシン効果が低減し、熱収縮率も高く
なる傾向がある。また、熱処理温度が140℃未満
であると、仮撚加工、撚糸加工時に断糸、毛羽が
発生し易く、アルカリ減量加工によつてシツク部
の強力が低下して、摩擦堅牢度が悪化し、更に沸
水収縮率が10%以上と依然として高く、良好な風
合の布帛が得られないので不適当である。一方、
熱処理温度が180℃を越えるとシツク部の脆化が
起りはじめ、加工時の断糸、毛羽が再び発生する
ようになると共に、アルカリ減量加工によつて、
更にシツク部の脆化が促進され、布帛としたとき
の摩擦堅牢度が著しく低下するので避けなければ
ならない。
この弛緩熱処理は、第1図に示すような段付加
熱ローラ6を用いて行なうのが、装着をコンパク
トにするので望ましいが、特にこれに限定される
ものではなく、周速の異なる一対のローラ間にヒ
ーターを設けて、その間で弛緩熱処理する方式
等、従来公知の弛緩熱処理方式を任意に採用する
ことができる。
このように、前記特定の速度で引取り、続いて
前記特定の温度及び倍率で延伸し、その後前記特
定の温度で弛緩熱処理することによつて、はじめ
て、優れたシツクアンドシン効果を有し、加工性
が良好で、アルカリ処理によつてもシツク部の強
力低下、摩擦堅牢度の悪化が起らず、しかも寸法
安定性が良好で熱収縮率の小さいシツクアンドシ
ンヤーンが得られるのであつて、上記条件のいず
れを欠いても本発明の目的は達成されない。
なお、第1図においては、交絡処理ノズル7を
段付加熱延伸ローラ6の下流に設けているが、こ
れはヤーンの解舒性を良好にするためであつて、
設けなくても差支えない。
かくして得られるシツクアンドシンヤーンは、
そのまま織編してもよく、また熱処理、再延伸熱
処理、仮撚加工、延伸仮撚加工等を施してもよ
い。
以下に実施例をあげて本発明を更に説明する。
実施例中におけるシツクアンドシンの評価は次の
ようにした。
1 シツクアンドシンの形態
シツクアンドシンヤーンを筒編にし、染料と
してイーストマンコダツクポリエステルネイビ
ーブルーを用いて、100℃の熱水中で染色し、
シツク部(濃染部)とシツク部(淡染部)のコ
ントラスト、割合、周期を観察した。
2 摩擦堅牢度
シツクアンドシンヤーンに2000T/Mの撚り
をかけ、ジヨーゼツトに製織後、沸水中で20分
間リラツクス処理し、次いで180℃で45秒間プ
レセツトを施し、その後、濃度35g/のカ性
ソーダ水溶液中で煮沸処理して、15%の減量処
理を行ない、次いで110℃で45分間、イースト
ポリエステルネイビーブルーを用いて染色し、
160℃で45秒間フアイナルセツトしたものをサ
ンプル布帛として使用する。
測定は、該サンプル布帛の上に、水で湿めし
た綿布(カナキン)を重ね合せ、学振型摩擦試
験器(昭和重器(株)製)にて、500gの荷重下で、
100回擦過した後、綿布にサンプル布帛から摩
耗、脱落した着色繊維がどの程度付着している
かを肉眼で判定し、1〜5級にランク付けする
ことにより行う。1級は多量の着色繊維が付着
していて摩擦堅牢度が悪いものであり、5級は
全く着色繊維の付着が認められず摩擦堅牢度が
良好なものである。級が大きくなるにつれて摩
擦堅牢度が良くなることを示す。
実施例1〜11及び比較例1〜6
艶消剤として0.3重量%の二酸化チタンを含有
する極限粘度0.65のポリエチレンテレフタレート
を、第1図に示す装置(但し、延伸ローラ6の下
流の交絡処理ノズル7は使用せず)を用いて296
℃で溶融吐出し、10個/mの交絡を噴射ノズル3
によつて付与し、第1表記載の引取速度及び予熱
ローラ温度に設定して引取ローラ5を介して8回
巻回して引取りつつ予熱し、引取ローラ4と段付
加熱延伸ローラ6とによつて第1表記載の倍率で
延伸すると同時に段付加熱延伸ローラ6により
160℃で2.0%の弛緩率にて熱処理を施して75デニ
ール/36フイラメントの9Kg捲きのパツケージと
して捲取つた。得られたシツクアンドシンヤーン
の評価結果は第1表に示す通りであつた。
The present invention relates to a method for producing thick-and-thin yarn made of polyester. Polyester thick-and-thin yarn, that is, polyester yarn consisting of single yarns with varying fineness, is used as a special yarn because the fabric obtained from it exhibits a unique texture, and when this fabric is dyed, it exhibits a marbled appearance. Are known. Conventionally, as a method for manufacturing polyester thick-and-thin yarn, there is a method in which the yarn tension is varied by changing the contact angle with a grooved roller or guide during spinning or drawing of the polyester yarn.
A method is known in which the ejection ratio of two components is changed when spinning a composite fiber made of the components. However, such a method requires a complicated apparatus and has poor productivity, so it is not implemented industrially. Also known is a method of forming a thick-and-thin yarn by stretching undrawn polyester yarn at an appropriate ratio and temperature. However, according to this method, the thick-and-thin pattern varies greatly depending on the aging of the undrawn yarn used. Furthermore, in this method, the thick-and-thin pattern varies greatly depending on the inner and outer layers of the undrawn yarn package used. Therefore, this method cannot stably produce yarn with a predetermined thick-and-thin pattern;
Cannot be used industrially. As a result of intensive research into a method for stably manufacturing a specified thick-and-thin yarn with high productivity without using special equipment, the present inventors melt-spun polyester and created a specific yarn without having to wind it up. I learned that the above objective could be achieved by taking it under certain conditions and then stretching it under certain conditions, so I proposed it earlier.
However, when the thick-and-thin yarn obtained by this method is subjected to false twisting or twisting, yarn breakage and fluffing are likely to occur, and furthermore, when subjected to alkali reduction processing, the strength of the thick part decreases and the fastness to friction deteriorates. The problem arises. In addition, it has poor dimensional stability and a high thermal shrinkage rate (boiling water shrinkage rate of 10% or more), so it has the disadvantage that the texture of the fabric becomes hard when subjected to heat treatment after being made into a fabric. Therefore, in order to solve these problems, the present inventors conducted further studies and found that after spinning and drawing under specific conditions, it is sufficient to perform heat treatment under specific conditions. Reached. That is, the present invention melts and discharges polyester.
Take off at a speed of 3500 m/min or less, then take it off at a temperature below the secondary transition point of polyester without winding it up, and use the following formula: 167/SS+1.21≦DR≦2100/SS+1.12 [In the formula, SS is taken off. Speed (m/min) and DR are stretching ratios (times). ] Stretched at a magnification that satisfies
This is a method for producing thick-and-thin yarn, which is characterized by heat treatment at a temperature of ~180°C and then winding. The polyester referred to in the present invention is mainly made of polyethylene terephthalate, but a part of the terephthalic acid component (usually 15 mol% or less) is used as a component of other dibasic acids, such as isophthalic acid, 5-sulfoisophthalic acid, adipic acid, etc. It may also be replaced with a part or all of the ethylene glycol component having 3 to 3 carbon atoms.
10 may be replaced by an alkylene glycol, especially butylene glycol, or may be partially replaced by a polyoxyalkylene glycol such as polyoxyethylene glycol. The degree of polymerization of such polyester should be appropriately selected depending on the type of polyester and the use of the product as a thick-and-thin yarn. Normally, in the case of polyethylene terephthalate, the intrinsic viscosity [η] determined from the value measured in an o-chlorophenol solution at 35°C is 0.55~
A value of 0.7 is preferred. When melt-extruding the above-mentioned polyester, it is not necessary to adopt any special means, and any method can be adopted, and any direct stretching method can be adopted for stretching subsequent to spinning, but usually , an oil supply roller, a fluid injection nozzle, a roller that also serves as a take-up roller and a preheating supply roller are installed in this order under the spinneret.
An apparatus in which a stepped hot-stretching roller is installed downstream of this roller is compact in terms of equipment and advantageous in manufacturing. FIG. 1 is a schematic diagram showing an example of a preferable direct stretching method, in which 1 is a spinning device, Y is a spun yarn,
2 is an oiling roller, 3 is a fluid injection nozzle, 4
5 is a take-up roller that also serves as a preheating roller, 5 is a separate roller, 6 is a stepped hot stretching roller, 7 is an entangling treatment nozzle, and 8 is a winder. The yarn Y spun from the spinning device 1 is applied with an oil agent by an oiling roller 2, and after being entangled by a fluid jet nozzle 3, it is sent to a take-up roller 4 preheated to a drawing temperature via a separate roller 5, and then passed through a separate roller 5. At the same time as it is wound and taken off at a predetermined speed, it is preheated to the stretching temperature, and the downstream stage-additional hot stretching roller 6
is stretched to a predetermined magnification, and then wound several times around a stepped heat-stretching roller 6 heated to a predetermined temperature to form a large diameter portion 6a and a small diameter portion 6b of the stretching roller 6.
heat treated under a relaxation rate based on the circumferential velocity of
Then, if necessary, the fabric is entangled by an entangling treatment nozzle 7 and wound into a winder 8. At this time, the number of entanglements provided by the fluid injection nozzle 3 is preferably in the range of 5 to 40 pieces/m. Further, by adjusting the number of confounds, it is also possible to control the pick-and-thin pattern. Note that the number of entanglements referred to here is the number of unopened fibers measured by placing yarns in water in which liquid paraffin is suspended. In addition, the take-up speed, that is, the surface speed of the take-up roller 4 is
It is necessary to keep the speed below 3500m/min. If the take-up speed is higher than 3500 m/min, the resulting yarn will have insufficient contrast between the thick and thin portions. If the take-up speed is too slow, productivity will decrease, so it is preferably 1000 m/min or more. The preheating temperature of the take-up roller 4, that is, the stretching temperature is as follows:
It should be below the secondary transition point of the polyester used. If the temperature is higher than the second-order transition point, the contrast of the thick-and-thin becomes small and the occurrence of the sick-and-thin also becomes unstable. In addition, if this temperature is set too low, this temperature will easily fluctuate depending on the ambient temperature, which will make the occurrence of thick-and-thin unstable.
It is preferable to do the above. If the stretching ratio is too low, the thick and thin portions become long, making it difficult to develop sufficient thick and thin. If the stretching ratio is increased, thick and thin will appear, but if it is increased too much, the difference between the thick and thin portions will become small. As a result of numerous experiments conducted by the present inventors, it has been determined that an appropriate stretching ratio must satisfy the above formula. In other words, the appropriate stretching ratio DR (times) differs depending on the drawing speed.
If the take-up speed is SS (m/min), it is necessary to satisfy the following formula: 167/SS+1.21≦DR≦2100/SS+1.12. This pick-up speed SS
FIG. 2 illustrates the range of appropriate stretching ratios (m/min). In addition, in the present invention, it is necessary to draw the spun yarn continuously without winding it once.
When the yarn is once wound up in the spinning process and then stretched, the shape of the thick-and-thin yarn changes over time as the yarn is drawn at the end, making it impossible to stably produce a thick-and-thin yarn with a certain shape. The thus obtained thick-and-thin yarn is subjected to heat treatment at a temperature of 140-180°C under relaxed conditions. This relaxation rate is not particularly limited, but is 5%
The following is commonly used, and 1 to 4% is particularly preferred. If the relaxation rate is too high, the orientation of the thick part will be disordered and there will be a tendency for embrittlement to occur.Furthermore, the yarn will become slack on the drawing and heat treatment equipment, making it difficult to draw it in a stable state.
There is a tendency for heat treatment to become impossible. Heat treatment during elongation or constant length causes thinning of the thick part,
The stick-and-thin effect tends to be reduced and the heat shrinkage rate also tends to increase. In addition, if the heat treatment temperature is less than 140°C, yarn breakage and fuzz will easily occur during false twisting and twisting, and the strength of the thick part will decrease due to the alkali weight reduction process, resulting in poor friction fastness. Furthermore, the boiling water shrinkage rate is still high at 10% or more, making it impossible to obtain a fabric with a good feel, making it unsuitable. on the other hand,
When the heat treatment temperature exceeds 180℃, the thick part begins to become brittle, yarn breakage and fluffing occur again during processing, and due to alkali weight reduction processing,
Furthermore, this should be avoided because it promotes embrittlement of the thick portion and significantly reduces the fastness to friction when made into a fabric. It is preferable to carry out this relaxation heat treatment using a stepped heat roller 6 as shown in FIG. 1, since it can be installed compactly, but it is not particularly limited to this. Any conventionally known relaxation heat treatment method can be employed, such as a method in which a heater is provided between the two and the relaxation heat treatment is performed therebetween. In this way, only by drawing at the specific speed, then stretching at the specific temperature and magnification, and then performing relaxation heat treatment at the specific temperature, can an excellent thick and thin effect be obtained. It has good processability, and even when treated with alkali, there is no decrease in the strength of the thick part or deterioration of fastness to friction, and it is possible to obtain a thick-and-thin yarn with good dimensional stability and low heat shrinkage. , the object of the present invention cannot be achieved without any of the above conditions. In FIG. 1, the entangling treatment nozzle 7 is provided downstream of the stepped hot stretching roller 6, but this is to improve the unwinding property of the yarn.
There is no problem even if it is not provided. The thus obtained pick-and-thin yarn is
It may be woven or knitted as it is, or may be subjected to heat treatment, re-stretching heat treatment, false twisting, stretching false twisting, etc. The present invention will be further explained with reference to Examples below.
The evaluation of the SHICK-N-THIN in the Examples was carried out as follows. 1 Form of Thick and Thin The Thick and Thin yarn is knitted into a tube and dyed in hot water at 100℃ using Eastman Kodak Polyester Navy Blue as the dye.
The contrast, ratio, and period between the thick areas (dark dyed areas) and thick areas (light dyed areas) were observed. 2 Rubbing fastness Thick-and-thin yarn was twisted at 2000T/M, woven into a jersey, relaxed in boiling water for 20 minutes, then preset at 180°C for 45 seconds, and then washed with caustic soda at a concentration of 35 g/m. boiling in an aqueous solution to reduce weight by 15%, then dyeing with yeast polyester navy blue at 110°C for 45 minutes;
Use the final set at 160°C for 45 seconds as a sample fabric. The measurement was performed by placing a cotton cloth (Kanakin) moistened with water on top of the sample fabric, and using a Gakushin type friction tester (manufactured by Showa Juuki Co., Ltd.) under a load of 500 g.
After rubbing 100 times, the extent to which the colored fibers that have worn off and fallen off from the sample fabric adhere to the cotton fabric is visually judged and ranked from 1 to 5. Grade 1 indicates that a large amount of colored fibers are attached and the fastness to rubbing is poor, and Grade 5 is that in which no colored fibers are observed at all and the fastness to rubbing is good. This indicates that as the grade increases, the abrasion fastness improves. Examples 1 to 11 and Comparative Examples 1 to 6 Polyethylene terephthalate having an intrinsic viscosity of 0.65 and containing 0.3% by weight of titanium dioxide as a matting agent was prepared using the apparatus shown in FIG. 7 is not used) and 296
Melt and discharge at ℃ and spray 10 entanglements/m from injection nozzle 3.
The film is applied by a roller, set to the take-off speed and preheating roller temperature listed in Table 1, wound 8 times through the take-off roller 5, and preheated while being taken off. Therefore, while stretching at the magnification shown in Table 1, the stepwise hot stretching roller 6
It was heat treated at 160° C. with a relaxation rate of 2.0% and wound into a 9 kg package of 75 denier/36 filament. The evaluation results of the obtained thick and thin yarn were as shown in Table 1.
【表】
表からも明らかなように、紡糸引取速度が3500
m/分を越える比較例1は、シツクアンドシンの
コントラストが不充分となるが紡糸引取速度が
3500m/分以下の場合(実施例1〜3)は、良好
なシツクアンドシン形態が得られる。また、延伸
温度(予熱ローラ温度)が、1800m/分の速度で
紡糸、引取つたポリエチレンテレフタレート未延
伸糸の2次転移点(80℃)より高い温度になると
(比較例2)、やはりシツクアンドシンのコントラ
ストが不良となる。更に引取速度と、延伸倍率と
が
167/S.S.+1.21≦D.R.≦2100/S.S.+1.12
なる関係を満足する場合(実施例1〜11)は良好
なシツクアンドシン形態が得られるが、上記関係
式を満足しない場合(比較例3〜6)は、シツク
アンドシン形態において、コントラスト不良が発
生する。
比較例 7〜10
実施例1で使用したと同じポリエチレンテレフ
タレートを、296℃で溶融押出し、第2表記載の
引取速度で引取つた後、5Kg捲の未延伸糸パツケ
ージに巻き上げ、温度25℃、湿度65%の雰囲気中
2日間及び30日間放置したものを、それぞれ予熱
ローラ温度65℃、延伸倍率1.4倍で延伸した。得
られたシツクアンドシンヤーンの評価結果は第2
表に示した通りであつた。なお、第2表中の「2
日経時」、「30日経時」はそれぞれ、未延伸糸パツ
ケージを2日経過後延伸した場合と30日経過後延
伸した場合を示すものである。
尚、「パツケージ内外層差」とは未延伸糸パツ
ケージの内層部と外層部におけるシツクアンドシ
ンの形態の差を意味する。[Table] As is clear from the table, the spinning take-off speed is 3500
In Comparative Example 1, when the speed exceeds m/min, the contrast of the thick-and-thin is insufficient, but the spinning take-off speed is
When the speed is 3500 m/min or less (Examples 1 to 3), a good pick-and-thin configuration can be obtained. In addition, when the drawing temperature (preheating roller temperature) becomes higher than the secondary transition point (80°C) of the undrawn polyethylene terephthalate yarn spun and taken at a speed of 1800 m/min (Comparative Example 2), the The contrast becomes poor. Furthermore, when the take-up speed and the stretching ratio satisfy the relationship 167/SS+1.21≦DR≦2100/SS+1.12 (Examples 1 to 11), a good thick-and-thin form can be obtained, but the above relational expression If the above conditions are not satisfied (Comparative Examples 3 to 6), poor contrast occurs in the thick-and-thin mode. Comparative Examples 7 to 10 The same polyethylene terephthalate as used in Example 1 was melt-extruded at 296°C, taken off at the take-off speed listed in Table 2, and wound into a 5 kg undrawn yarn package at a temperature of 25°C and humidity. The samples were left in a 65% atmosphere for 2 days and 30 days, and then stretched at a preheating roller temperature of 65°C and a stretching ratio of 1.4 times. The obtained evaluation results of the Thick and Thin Yarn are the second
It was as shown in the table. In addition, “2” in Table 2
"Time after 30 days" and "Time after 30 days" indicate the cases where the undrawn yarn package was stretched after 2 days and when it was stretched after 30 days, respectively. The term "difference between the inner and outer layers of the package" means the difference in the shape of the thick-and-thin layer between the inner layer and the outer layer of the undrawn yarn package.
【表】【table】
【表】
未延伸糸の経時によつて、シツクアンドシンの
形態が変化すると共に、パツケージの内外層で
も、シツクアンドシン形態に差が生じ、一定の形
態を有するシツクアンドシンヤーンを安定に製造
することができない。
実施例12〜16、比較例11〜13
実施例1で使用したポリエチレンテレフタレー
トを第1図に示す装置を用いて295℃で溶融吐出
し、15個/mの交絡を噴射ノズル3によつて付与
し、50℃に加熱された引取ローラ4によつて2000
m/分の速度で引取つた後、該引取ローラ4と段
付加熱延伸ローラ6との間で1.8倍に延伸した。
次いで、段付加熱延伸ローラ6での弛緩率及び
該段付加熱延伸ローラ6の温度を第3表記載の通
り変更して、弛緩熱処理を施し、ワインダー8に
巻取つた。得られたシツクアンドシンヤーンの評
価結果を第3表に示す。[Table] As the undrawn yarn ages, the shape of the thick-and-thin changes, and differences occur in the shape of the thick-and-thin between the inner and outer layers of the package, making it difficult to stably produce thick-and-thin yarn with a constant shape. Can not do it. Examples 12 to 16, Comparative Examples 11 to 13 The polyethylene terephthalate used in Example 1 was melted and discharged at 295°C using the apparatus shown in Fig. 1, and 15 entanglements/m were imparted by the injection nozzle 3. 2000℃ by the take-up roller 4 heated to 50℃.
After being taken off at a speed of m/min, the film was stretched to 1.8 times between the take-off roller 4 and the stepped hot stretching roller 6. Next, the relaxation rate at the stepped hot-stretching roller 6 and the temperature of the stepped hot-stretching roller 6 were changed as shown in Table 3, a relaxation heat treatment was performed, and the film was wound into a winder 8. Table 3 shows the evaluation results of the obtained thick and thin yarn.
【表】【table】
【表】
糸条を弛緩させることなく定長で熱処理した比
較例11では、シツク部とシン部のコントラストが
不良となりシツクアンドシンの形態が悪化し、沸
水収縮率も高目になる。また、熱処理温度が140
〜180℃の範囲外になると(比較例8、9)加工
性が悪くなると共に摩擦堅牢度が低下する。特に
熱処理温度が140℃未満の場合(比較例12)は、
沸水収縮率が10%以上となり、この糸を使つた布
帛は風合が硬くなるという欠点が生ずる。これに
対して、140〜180℃の温度範囲で弛緩熱処理を施
した場合(実施例12〜16)は、加工性、摩擦堅牢
度共に良好で、沸水収縮率が低く、シツクアンド
シンヤーン形態が良好なシツクアンドシンヤーン
が得られる。[Table] In Comparative Example 11, in which the yarn was heat-treated at a constant length without relaxing it, the contrast between the thick part and the thin part was poor, the thick and thin form deteriorated, and the boiling water shrinkage rate was high. In addition, the heat treatment temperature is 140
When the temperature is outside the range of ~180°C (Comparative Examples 8 and 9), processability deteriorates and abrasion fastness decreases. Especially when the heat treatment temperature is less than 140℃ (Comparative Example 12),
The boiling water shrinkage rate is 10% or more, and fabrics using this yarn have the disadvantage of having a hard texture. On the other hand, when relaxation heat treatment was performed in the temperature range of 140 to 180°C (Examples 12 to 16), both processability and abrasion fastness were good, boiling water shrinkage was low, and the thick-and-thin yarn form was good. A good pick-and-thin yarn can be obtained.
第1図は本発明を実施するに適した装置の一例
を示す簡略図であり、第2図は紡糸速度S.S.
(m/分)に対する適正延伸倍率(倍)の範囲を
示す図表である。
3は流体噴射ノズル、4は予熱供給ローラを兼
ねた引取ローラ、6は段付加熱延伸ローラであ
る。
FIG. 1 is a simplified diagram showing an example of an apparatus suitable for carrying out the present invention, and FIG. 2 shows a spinning speed SS.
It is a chart showing the range of appropriate stretching ratio (times) with respect to (m/min). 3 is a fluid jet nozzle, 4 is a take-up roller that also serves as a preheating supply roller, and 6 is a stepped hot stretching roller.
Claims (1)
の速度で引取り、引続いて一旦巻取ることなくポ
リエステルの二次転移点以下の温度及び下記式 167/S.S.+1.21≦D.S.≦2100/S.S.+1.12 〔式中、S.S.は引取速度(m/分)、D.S.は延伸
倍率(倍)である。〕 を満足する倍率で延伸し、更に弛緩状態にて140
〜180℃の温度で熱処理してから巻取ることを特
徴とするシツクアンドシンヤーンの製造方法。[Claims] 1. Polyester is melted and discharged and taken up at a speed of 3500 m/min or less, and then the temperature is below the secondary transition point of the polyester without being wound up once, and the following formula 167/SS+1.21≦DS ≦2100/SS+1.12 [In the formula, SS is the drawing speed (m/min) and DS is the stretching ratio (times). ] Stretched at a magnification that satisfies
A method for producing thick-and-thin yarn characterized by heat treatment at a temperature of ~180°C and then winding.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8253581A JPS57199813A (en) | 1981-06-01 | 1981-06-01 | Production of thick and thih yarn |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8253581A JPS57199813A (en) | 1981-06-01 | 1981-06-01 | Production of thick and thih yarn |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57199813A JPS57199813A (en) | 1982-12-07 |
JPS6347803B2 true JPS6347803B2 (en) | 1988-09-26 |
Family
ID=13777193
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8253581A Granted JPS57199813A (en) | 1981-06-01 | 1981-06-01 | Production of thick and thih yarn |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57199813A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60134019A (en) * | 1983-12-21 | 1985-07-17 | Toray Ind Inc | Direct spinning and drawing of polyester yarn |
JPS63182412A (en) * | 1987-01-26 | 1988-07-27 | Asahi Chem Ind Co Ltd | Production of thick-and-thin yarn |
US4906519A (en) * | 1988-06-06 | 1990-03-06 | Basf Corporation | Variable denier filaments and method of producing same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5184918A (en) * | 1975-01-17 | 1976-07-24 | Toray Industries | ENSHINHOHO |
JPS551333A (en) * | 1978-06-16 | 1980-01-08 | Toray Industries | Production of special multifilament yarn |
-
1981
- 1981-06-01 JP JP8253581A patent/JPS57199813A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5184918A (en) * | 1975-01-17 | 1976-07-24 | Toray Industries | ENSHINHOHO |
JPS551333A (en) * | 1978-06-16 | 1980-01-08 | Toray Industries | Production of special multifilament yarn |
Also Published As
Publication number | Publication date |
---|---|
JPS57199813A (en) | 1982-12-07 |
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