JPS5966582A - Mono-bath dyeing of mixed article - Google Patents

Mono-bath dyeing of mixed article

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Publication number
JPS5966582A
JPS5966582A JP57173677A JP17367782A JPS5966582A JP S5966582 A JPS5966582 A JP S5966582A JP 57173677 A JP57173677 A JP 57173677A JP 17367782 A JP17367782 A JP 17367782A JP S5966582 A JPS5966582 A JP S5966582A
Authority
JP
Japan
Prior art keywords
fibers
dyeing
bath
fiber
dye
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
Application number
JP57173677A
Other languages
Japanese (ja)
Inventor
武居 庄治
康弘 木下
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP57173677A priority Critical patent/JPS5966582A/en
Publication of JPS5966582A publication Critical patent/JPS5966582A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明はセルロース系繊維とポリエステル繊維とを含有
する混用品(以下単に混用品という。)の−浴染色法に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a bath dyeing method for a mixed product containing cellulose fibers and polyester fibers (hereinafter simply referred to as a mixed product).

従来、混用品の染色には二浴染色法が用いられている。Conventionally, a two-bath dyeing method has been used for dyeing mixed products.

すなわち、第−浴で分散染料でポリエステル繊維を目的
の色相に染色し、中間に還元洗浄を施してポリエステル
繊維の表面染着染料、およびセルロース繊維に汚染した
分散染料を分解除去し、さらに第二浴目でセルロース繊
維を直接染料又は反応性染料で染色するという非常に煩
雑・な染色法を用いていた。この様に一浴目と二浴目と
の間に還元洗浄を入れて二浴染色を実施する理由は以下
のとおりである。すなわち−浴目のポリエステル繊維の
分散染料染色時に、セルロース系繊維が分散染料によっ
て汚染され、このセルロース繊維への汚染分散染料が混
用品の染色堅牢度を低下さセるためである。又、この汚
染分散染料は染色バッチ毎にその程度はばらつくもので
あり、二浴目でセルロース繊維を直接染料又は反応性染
料で目標色相に合わせることが非常に困難となるためで
ある。
That is, in the first bath, polyester fibers are dyed to the desired hue with disperse dyes, and in the middle, reduction washing is performed to decompose and remove the dyes dyed on the surface of the polyester fibers and the disperse dyes that have contaminated the cellulose fibers. A very complicated dyeing method was used in which cellulose fibers were dyed with direct dyes or reactive dyes in the bath. The reason why two-bath dyeing is performed by inserting reduction washing between the first and second baths is as follows. That is, when dyeing polyester fibers with disperse dyes, the cellulose fibers are contaminated with the disperse dyes, and the disperse dyes that stain the cellulose fibers reduce the color fastness of the mixed product. Moreover, the degree of this staining disperse dye varies from dyeing batch to dyeing batch, and it is very difficult to match the target hue to the cellulose fibers with direct dyes or reactive dyes in the second bath.

ここで分散染料と直接染料又□は分散染料と反応性染料
との混合染色浴を用いてこれら混用品を−浴法で染色し
、その後還元洗浄を行なえばよいと考。
Here, it is thought that it is possible to dye these mixed products using a mixed dyeing bath of disperse dyes and direct dyes, or □ of disperse dyes and reactive dyes, and then perform reduction washing.

えられるが、分散染料と直接染料との組み合わせ7.、
合ンヤ7L;” ”o ’ −’;l系繊・維い汚染、
た亦門門料、1除去して堅牢度4能をゆ土さ”るにはセ
ル・−ス 、。
However, the combination of disperse dye and direct dye7. ,
Ainya 7L;""o'-';L fiber/fiber contamination,
It is necessary to remove 1 and remove 4 properties of fastness by using cellulose.

系繊維に染着した直接染料の脱落を起こす程度の□強力
な処理条件で還元洗浄をすることが必要となり、結局セ
ルロース系繊維側を目標の色相にすることが困難となる
。一方分散染料と反応性染料との組み合わせの一浴で□
染色する場合\ポリ亜ステ □ル繊維を目標の色相に染
着させる温度(通常/、30°C)では市販の反応性染
料の多くは熱分解してしまい、セルロース系繊維を目標
色相に染色することができない。以上のこじから従来技
術では側繊維混用品を目標の色に堅牢に染色するには二
浴法をとらざるを得ず、合理的な一浴法が実行できるの
はポリエステル繊維側を未染色で残す色柄染色品の場合
のみであった。
It is necessary to perform reduction cleaning under strong treatment conditions that cause the direct dye dyed on the cellulose fibers to come off, and it becomes difficult to achieve the target hue on the cellulose fiber side. On the other hand, in a bath of a combination of disperse dye and reactive dye □
When dyeing\Polyester □At the temperature at which cellulose fibers are dyed to the target hue (usually 30°C), most commercially available reactive dyes decompose thermally, making it difficult to dye cellulose fibers to the target hue. Can not do it. As a result of the above, conventional techniques have no choice but to use a two-bath method in order to dye side-fiber-mixed products to the target color in a durable manner, and a rational one-bath method is only possible when the polyester fiber side is undyed. This was only in the case of dyed products with colored patterns.

本発明者らはこれらの問題を解決し、混用品を堅牢に染
色する一浴法について鋭意検討した結果、セルロース系
繊維に分散染料が殆んど汚染せず1、、竹?直接染料又
91反応1染11E’j (7) * ′b *  Z
 M tf& lik染色条件内で分散染料により良好
に染色されるポ□    、、。
The inventors of the present invention solved these problems and conducted intensive studies on a one-bath method for dyeing blended products in a durable manner.As a result, the disperse dye hardly contaminates the cellulose fibers.1.Bamboo? Direct dye or 91 reaction 1 dye 11E'j (7) * 'b * Z
□, which dyes well with disperse dyes within Mtf&lik dyeing conditions.

リエメテル繊維を見い出すことにより本発明に、達した
The present invention was achieved by discovering riemeter fibers.

すなわち本発明は、混用品を一浴で染色するに際し、該
ポリエステル繊維が実質的にポリエチレンテレフタレー
トよりなり、測定周波数/ / OHy、における力学
的損失正接(tanδ)のピーク温度(’l”max)
(°C)がlo’z°C以下で、かつ−δのピーク値(
−δ)maXが0.08を越える構造特性を有するポリ
エチレンテレフタレート繊維、を用いれば分散染料によ
るセルロース系繊維の汚染が少なくなり、堅牢な混用品
染色物を得られることがわかり、本発明に至った。
That is, in the present invention, when dyeing a mixed product in one bath, the polyester fiber is substantially made of polyethylene terephthalate, and the peak temperature ('l''max) of the mechanical loss tangent (tan δ) at the measurement frequency / / OHy.
(°C) is below lo'z°C, and the peak value of -δ (
-δ) It was found that using polyethylene terephthalate fibers having a structural characteristic of ma Ta.

本発明で君うポリエチレンテレフタレートとは、エチレ
ンテレフタレートを繰返し単位とした線状重合物で、第
三読分としてイソフタル酸、スルホン化イソフタル酸の
ナトリウム塩、ポリエチレングリコールなどを重量比で
s%未満を共重合せしめてなるものを含む。又、通常合
成繊維に添加される艶消剤、安定剤、制電剤などを含ん
でもよい。
The polyethylene terephthalate used in the present invention is a linear polymer with ethylene terephthalate as a repeating unit, and the third component is isophthalic acid, sodium salt of sulfonated isophthalic acid, polyethylene glycol, etc. in a proportion of less than s% by weight. Including those formed by copolymerization. It may also contain matting agents, stabilizers, antistatic agents, etc. that are usually added to synthetic fibers.

又、重合度については通常の繊□維形成用の範囲であれ
ば特に薊限はない。
Furthermore, there is no particular limit to the degree of polymerization as long as it is within the range for normal fiber formation.

従来、ボ1′Jエステルより去る衣料用繊維は、紡速コ
θOcm/4)以下で紡糸された未延伸繊維を3〜S倍
に延伸して製造していた。この様な延伸糸は、極めそ強
固な舶楚形領域を有し、測定周波数/1011zにおけ
名力学的抗失正接(fanδ)のピーク温度(Tmax
)は7.2 h〜/ 、? s”C付近にあり、分散染
料でハ?O℃付近の高温下で染色され、染色後のTm 
axも/2A’〜/ 3 !r’c付近にある。
Conventionally, clothing fibers from Bo1'J esters have been produced by drawing undrawn fibers spun at a spinning speed of θOcm/4) or less by a factor of 3 to S. Such a drawn yarn has an extremely strong wave-shaped region, and has a peak temperature (Tmax) of the nominal mechanical anti-loss tangent (fan δ) at the measurement frequency /10
) is 7.2 h~/,? s”C, dyed with disperse dye at high temperature around 0℃, Tm after dyeing
Ax is also /2A'~/3! Located near r'c.

最近生産性の面から紡糸工程のみで延伸せずにt)(維
を得る、いわゆるPOYあるいは高速紡糸繊維と言った
省力化を図った方法□が徐々に採用されつつある。
Recently, from the viewpoint of productivity, labor-saving methods such as so-called POY or high-speed spinning fibers, in which fibers are obtained only in the spinning process without drawing, are gradually being adopted.

1)OYと称するものは、はぼ3oOOV分程度の紡速
で紡糸された繊維であって□、延伸仮□撚工程でもって
延伸と仮燃を同時に行ない嵩高糸を得るための原糸であ
る。この様なPOYよ□り得られた嵩高糸の(幼nδ)
max は染色前後において0. / 0付近、Tni
AxはTmaxは90″C付近にあるが染色中に30%
を越える収縮率を示し、染色前後において、?(7′C
における初期モジュラスはs Of/d未満である。し
かも、引張強度は−r/d以下、伸度はざ0%以上あり
衣料用繊維としては実用に供されていない。  ・又、
高速紡糸繊維すなわち紡速が’1000m/分〜t00
0m/分で紡糸され、延伸されていない繊維は、(ta
fIδ)maxはおおむね0. / 0以上、Tmax
は/10〜//3″C付近にあるが、700〜130℃
で染色された後め(taiδ)maxはo、tyg〜θ
/ンで、Tmaxは/ / & 〜/ 2.11”Cに
なる。すなわち染色中に熱水の作用により微細構造が変
化する。
1) What is referred to as OY is a fiber spun at a spinning speed of approximately 3 oOOV minutes, and is a raw yarn for obtaining bulky yarn by simultaneously performing drawing and pre-twisting in the drawing and pre-twisting process. . Bulky yarn obtained from such POY (young nδ)
max is 0. before and after staining. / around 0, Tni
Ax and Tmax are around 90″C, but 30% during staining.
Showing a shrinkage rate exceeding ? before and after staining? (7'C
The initial modulus at is less than s Of/d. Furthermore, the tensile strength is less than -r/d and the elongation is more than 0%, so it is not put to practical use as a clothing fiber. ·or,
High speed spun fibers, that is, spinning speed is 1000 m/min ~ t00
Fibers spun at 0 m/min and not drawn are (ta
fIδ)max is approximately 0. / 0 or more, Tmax
is around /10~//3''C, but 700~130℃
The tai δ max stained with is o, tyg ~ θ
/n, Tmax becomes / / & ~/ 2.11"C. That is, the microstructure changes due to the action of hot water during dyeing.

したがって、従来ポリエステル繊維で本発明に言う如き
測定周波数/ / ’OHzにおけるiδのピーク温度
Tmax (”C)が105℃以下で、かつ−δのピー
ク値(−δ)がo、ogを越える構造特性を有し、衣料
用繊維として実用化されているものは存在しなかった。
Therefore, conventional polyester fibers have a structure in which the iδ peak temperature Tmax ("C) at the measurement frequency / / 'OHz as referred to in the present invention is 105°C or less, and the -δ peak value (-δ) exceeds o, og. There were no fibers with these characteristics that had been put to practical use as clothing fibers.

分散染料がポリエステル繊維に染着するのは、その無定
形領域である。無定形領域の構造を表現する特性値とし
て、上記Tmaxと(tallIδ)maxの値が適切
である。
It is in the amorphous region that the disperse dye dyes the polyester fiber. The values of Tmax and (tallIδ)max are suitable as characteristic values expressing the structure of the amorphous region.

T maxは通常ガラス転移温度の約りO′C高濡に位
置し、(tarlδ)maxは、、温度Tmaxにおけ
る熱運動の活発化した無定形領域内の分子鎖の量に関係
する。
T max is usually located at an O'C high temperature around the glass transition temperature, and (tarl δ) max is related to the amount of molecular chains in the amorphous region with activated thermal motion at the temperature T max.

本発明において、Tmaxおよび(−δ)rnaxは無
定形領域内部の、分子鎖のミクロブラウン運動に原因し
て発現する力学吸、収(αa吸収)に関する値を意味す
る。したがって定性的−は(勧δ)maxが大きいほど
無定ゎ領域t 6を多く’、’rl′。687.低いや
1、無定う領域内の分子鎖のミクロンラウン運動が低温
で活発化し、分散染料が低温で染まり易くなる。  □
本発明者らは、分散染實がポリエステル繊維内□部−浸
透、拡散する現象が(−δ)maxおよびT+naxと
密接に関係し、さらに分散染料によるセルロース系維へ
の汚染に力える影響を検討した結果、本発明に達した。
In the present invention, Tmax and (-δ)rnax mean values related to mechanical absorption (αa absorption) caused by micro-Brownian motion of molecular chains inside the amorphous region. Therefore, qualitatively, the larger the (recommendation δ)max, the more the indeterminate area t6', 'rl'. 687. At a low temperature of 1, the micron round motion of the molecular chains within the indeterminate region becomes active at low temperatures, making it easier for disperse dyes to dye at low temperatures. □
The present inventors have discovered that the phenomenon in which disperse dyes permeate and diffuse into polyester fibers is closely related to (-δ)max and T+nax, and that the effect of disperse dyes on contamination of cellulose fibers is closely related to (-δ)max and T+nax. As a result of study, we have arrived at the present invention.

すなわち、ポリエステル繊維の測定周波数//θHzに
おける(−δ)maxの値がo、ogを越え、かつTm
axが/ 0 、t”C以下であれば、分散染料の染着
性がよく、一方、セルロース系繊維への分散染料汚染も
少なくなる。
That is, the value of (-δ)max at the measurement frequency //θHz of polyester fiber exceeds o, og, and Tm
When ax is / 0 , t''C or less, the dyeability of the disperse dye is good, and on the other hand, staining of the cellulose fibers with the disperse dye is reduced.

本発明のセルロース系繊維とは、ビスツースレーヨン、
キュプラレーヨン、ポリノジックレーヨン等の再生セル
ロースm#および綿、麻等の天然繊維を含むものである
。セルロース系繊維およびポリエステル繊維は長繊維、
短繊維のいずれでもよく、これらは混紡、混繊、交撚、
交編、交織等いずれの混用形態をも含むものであり、そ
の混用比率は、少なくともS重量%以上である。
The cellulose fibers of the present invention include bistoothrayon,
It contains regenerated cellulose m# such as cupra rayon and polynosic rayon, and natural fibers such as cotton and hemp. Cellulose fibers and polyester fibers are long fibers,
Any short fibers may be used, and these may be blended, blended, intertwisted,
It includes any mixed forms such as mixed knitting and mixed weaving, and the mixing ratio thereof is at least S weight % or more.

本発明法の混用品は、セA−ロース系繊維およびポリエ
ステル繊維を各々S重量%以上含んでいるものであり、
その他ポリアミド繊維、ボリプ四ピレン繊維、アクリル
繊維等の合成繊維や絹、羊毛等の天然繊維を第3、第グ
成分として含有していても差し支えない。
The mixed product produced by the method of the present invention contains S A-loin fiber and polyester fiber each in an amount of S weight % or more,
Other synthetic fibers such as polyamide fibers, polypyrene fibers, acrylic fibers, and natural fibers such as silk and wool may also be contained as the third and fourth components.

本発明法の一浴染色法とは、セルロース系m維用染料と
ポリエステル繊維用染料とを同浴に添加して一つの洛中
で両繊維を同時に染色することを意味し、−浴目の途中
で染色浴の条件を変化させる方”法′(−浴□二門法)
を含むも゛のである。
The one-bath dyeing method of the present invention means that a cellulose textile dye and a polyester fiber dye are added to the same bath and both fibers are dyed simultaneously in one bath. A method of changing the conditions of the dyeing bath (-bath □ two gate method)
It also includes.

本□発明の□方法においぞ染色が終了した時点で、分散
染□料窃銘′柄、使用1度によっては若生セルロース系
繊維1が汚染される場合がある。こ□の程度の汚染“染
□料”’tri’、セルロース系繊維に染着した直接染
料又は反応性染料に退色等の損傷を与えない温和な還元
洗浄又はソーピングを実施することで除去が可能であり
、堅牢度向上およびセルロース系繊維の目標色□達成が
可能となる。
When the dispersion dyeing is completed in the method of the present invention, the young cellulose fiber 1 may be contaminated depending on the type of dispersion dye stolen or once used. This degree of contamination can be removed by mild reduction cleaning or soaping that does not cause damage such as fading to the direct dyes or reactive dyes dyed on cellulose fibers. This makes it possible to improve the fastness and achieve the target color □ of cellulose fibers.

本発明で言うような構造特性を有するポリエステル繊維
は、紡速11000m1分以上で紡糸した未延伸ポリ、
エステル$a1iaを、220℃乃至300℃に加熱し
た乾熱空気中又仲過熱水蒸気中又は、両者の混合雰囲気
中で熱処理することにより得られる。なおこの際、繊維
に掛る張力は/ f/d以下、にする必要がある。この
得られたポリエステル繊維は、そのままか、又は常法に
より仮撚加工するか、紡績原料としてのトウ、ステーブ
ルファイバーにしてもその構造特性は変らず、本発明の
範囲に含まれる0 次にJ本発明を構成するポリエチレンテレラタレート繊
維の力□学的損失正接(tar+δ)の測定法を示す。
Polyester fibers having the structural characteristics as referred to in the present invention include undrawn polyester fibers spun at a spinning speed of 11,000 m/min or more;
It is obtained by heat-treating ester $alia in dry hot air heated to 220° C. to 300° C., in medium superheated steam, or in a mixed atmosphere of both. At this time, the tension applied to the fibers needs to be less than /f/d. The obtained polyester fiber may be used as it is, or may be false-twisted by a conventional method, or may be made into tow or stable fiber as a spinning raw material without changing its structural characteristics and is within the scope of the present invention. J A method for measuring the mechanical loss tangent (tar+δ) of the polyethylene terelatate fiber constituting the present invention is shown.

東洋ポールドウ□イン社製レオパイブロン(Rhco−
vibron ) DDV−nc型動的粘弾性測定装置
を用い、試料約0.7 =、 、測定周波数/10H9
、昇温速度10”ヴ分で乾燥空気中にて各湿度における
ーδを測定する。
Toyo Pole Do□In Co., Ltd. Rheo-Pybron (Rhco-
Vibron) Using a DDV-NC type dynamic viscoelasticity measurement device, the sample was approximately 0.7 =, , measurement frequency/10H9
, -δ at each humidity is measured in dry air at a temperature increase rate of 10''.

勧δ一温度曲線から−δのピーク温度(Tmax ) 
(”C)と、ピーク値〔(−δ)max 〕  が得ら
れる。
-δ peak temperature (Tmax) from the recommended δ-temperature curve
(''C) and the peak value [(-δ)max] are obtained.

次に、実施例を挙げて本発明の詳細な説明する。Next, the present invention will be explained in detail by giving examples.

実施例1 紡速<100θm/分で紡糸されたポリエチレンテレフ
タレート繊維左Od/21/、tを2グざ°Cの空気中
でθgs秒□間、糸に掛かる張力を□0.0’3V/d
に規制し熱処理した( ’Tmax ’ / 0 ”C
+(−δ)max O,、Lo 9 ] 6又同時に比
較□のため紡速13θorn/分で、紡糸後30”Cで
33倍に延伸した!r Od/ 2(1’の繊維につい
ても同様に熱処理した〔Tmax : / l A”C
,(−δ)mayθ/−り〕。これら繊維のそれぞれを
ベソベル・グ(層化成製、、再生セルロース繊維) 、
s odと共に混用率(SQ%/SO%)で常法により
ストライプ柄の交編l・リコットに編立てた。
Example 1 Polyethylene terephthalate fibers spun at a spinning speed of <100 θm/min (Left Od/21/, t = 2 gps) Tension applied to the yarn was □0.0'3 V/ in θgs seconds □ in air at °C. d
('Tmax' / 0"C)
+(-δ)max O,, Lo 9 ] 6 Also for simultaneous comparison □, the spinning speed was 13θorn/min, and after spinning, the fiber was drawn 33 times at 30"C!r Od/2 (same as for 1' fiber) Heat treated to [Tmax: / l A”C
, (-δ) may θ/-ri]. Each of these fibers is made of besobel (layer chemically made, regenerated cellulose fiber),
It was knitted into a striped pattern interlaced l/ricott by a conventional method using a mixed ratio (SQ%/SO%) with s od.

こhら編地を780″c、  lIo秒間乾熱セットし
た後、下記染色条件でそれぞ:れ染色し、続い”Cソー
ピング、フィックス処理を行ない、さらに/90″Cx
1Iθ秒乾熱セットして仕」二けた。これら染色編地の
堅牢度およびベンベルブ繊維部分の汚染度を表/に、示
した。
After dry heat setting these knitted fabrics at 780"C for 10 seconds, they were dyed under the following dyeing conditions, followed by "C soaping and fixing treatment, and then /90"Cx.
I set it to dry heat for 1Iθ seconds and finished it. Table 1 shows the fastness of these dyed knitted fabrics and the degree of contamination of the benvelub fibers.

〈染色条件〉 染  料二分散染料 ダイアニツクスポルドーGR−8F(三菱化成製)13
%0@ ・ 直接染料 カヤラススブラルビンl(日本化革製)/、O%owf 助    剤: 芒   硝            
 /−2鳴owfデモールN(第−工業製薬製)/f/
1染色泪度:/θO℃、/30℃ 染色時間=60分 浴    比 :/:、20.: 〈ソービイグ〉 。
<Dyeing conditions> Dye bidisperse dye Dianic Spordo GR-8F (manufactured by Mitsubishi Kasei) 13
%0@ ・ Direct dye Kayarasu Subralbin l (made by Nippon Kazai Co., Ltd.) /, O%owf Auxiliary agent: Glauber's salt
/-2owf Demol N (manufactured by Dai-Kogyo Seiyaku) /f/
1 Dyeing depth: /θO℃, /30℃ Dyeing time = 60 minutes Bath ratio: /:, 20. :〈Soubiig〉.

、 炭酸ソーダ           0.A;Y/l
・□ スコアo −ル、 FC−2!;0 (花王アトラス製
) 7に、、、f/lり00×、20分 〈フィックス処理〉 7二9Lカツa7KP(ElゆイtJJ)”  Q%o
vrflfxコθ分       □ 表    /′ 水堅牢度 : JIS−L−OgllA(B法)汚染度
(級):汚染用グレースケール判定・  (5級):汚
染少  (7級):汚染天衣/かられかる様に、本発明
法の染色編地はいずれの染色湿度でも汚染性、堅牢度が
良好であるのに対し、本発明法外の比較、トリフット編
地の場合、/θO″C,染色ではポリエステル繊維部分
の発色性が不十分であり、ベンベルブ繊維部分は堅牢度
、汚染性いずれも不十分である。又これを/30°C染
色したものはポリエステル繊維部分の発色性は十分とな
るものの、ベンペルグ繊維側の堅牢度、汚染性は著しく
低いものしか得られなかった。
, carbonated soda 0. A;Y/l
・□ Score o-ru, FC-2! ;0 (manufactured by Kao Atlas) 7, f/l 00x, 20 minutes <Fix processing> 729L cut a7KP (El Yui tJJ)" Q%o
vrflfx θ min □ Table /' Water fastness: JIS-L-OgllA (Method B) Contamination degree (grade): Gray scale judgment for contamination (Grade 5): Low contamination (Grade 7): Contaminated heaven/from As can be seen, the knitted fabric dyed using the method of the present invention has good stain resistance and fastness at any dyeing humidity, whereas in the case of the tri-foot knitted fabric using the method other than the method of the present invention, /θO″C, dyeing In this case, the color development of the polyester fiber part is insufficient, and the fastness and stain resistance of the benvelub fiber part are insufficient.Also, when this is dyed at /30°C, the color development of the polyester fiber part is sufficient. However, the fastness and stain resistance of the Bemperg fibers were only extremely low.

実施例コ 実施例/の紡速7000m7%糸の熱処理系を、仮撚ヒ
ーター長o、 g 1nを有する仮撚加工機にて、仮撚
ヒータ一温度、200℃に設定し、スピンドルに該糸条
を引掛は撚数11000t/m、延伸比11.:19 
、糸速、/9(。
The heat treatment system for the 7% yarn at a spinning speed of 7000 m and 7% in Example 1 was set to 200° C. with a false twisting heater length o and g 1n, and the yarn was placed on the spindle. The number of twists is 11,000t/m, and the stretching ratio is 11. :19
, yarn speed, /9(.

V分で仮撚加工、した。又同時比較の紡速i、yoom
Z分糸の熱処理系も同様仮撚機にて仮撚ヒータ一温度を
2.20℃に設定し、スピンドルに該糸条を引掛け、撚
数’I 000 Vm %延伸比0.970.糸速/、
2θm/7f+ 、 ’9仮撚加工した。これら加工糸
のそれぞれを、ベンベルブ(脂化成製再生セルロース繊
維)qo、dと共に、経、ポリニス、チル繊維1.緯ベ
ンベルグ繊維の交織り7タに常法にて製織した。これら
の織物を/70.’C・×30秒間乾熱セットした後、
下記栄件で紡速。
False twisting was performed for V minutes. Also, the spinning speed i, yoom of simultaneous comparison
The heat treatment system for the Z-divided yarn was similarly set using a false twisting machine, with the temperature of the false twisting heater set at 2.20°C, and the yarn was hooked onto the spindle, with the number of twists 'I 000 Vm % drawing ratio 0.970. Yarn speed/
2θm/7f+, '9 false twisting process. Each of these processed yarns, along with Benbelb (regenerated cellulose fiber manufactured by Fukkasei) qo and d, were used as warp, poly varnish, and chill fiber 1. Seven tassels of weft Bemberg fibers were woven in a conventional manner. These fabrics /70. 'C・× After dry heat setting for 30 seconds,
The spinning speed is as below.

11000 m/’t3−糸タフタiま、染色湿度/ 
00.7Gで、又紡速/′300″′分糸1y、p、+
i染色温度″′”C,3よ一/3゜°Cでそれぞれ染色
し、グO′Cで70分間湯洗、続いてソーピングした後
、/gO”cXJO秒間乾、熱セットして仕上げた。
11000 m/'t3-yarn taffeta, dyeing humidity/
00.7G, spinning speed/'300''' yarn 1y, p, +
i dyed at a dyeing temperature of ``''C, 3 to 1/3°C, washed in hot water for 70 minutes at GUO'C, then soaped, dried for 2 seconds at /gO'C, and finished by heat setting. .

〈染色条件〉 染  料:分散染料 ダイア二゛ンクスネービーブル−、!R−8!、(三菱
化成製)/2q%− 反応染料 (サント′社製)” ’   i 7 Q % owf
助    剤 : 芒    硝  左Of/l   
      ’ソーダ灰 7%owf 染色時間:各温度×グよ分      :浴    比
 : / : 2θ 〈ソーピング条件〉 モノゲン /グ/l    900×、lO’これら各
染色タフタ織物の堅牢度および発色性を表−に示した。
<Dyeing conditions> Dye: Disperse dye Diamond Navy Blue! R-8! , (manufactured by Mitsubishi Kasei) / 2q% - Reactive dye (manufactured by Santo')
Auxiliary agent: mirabilite left Of/l
'Soda ash 7%owf Dyeing time: Each temperature It was shown to.

表−かられかる様に本発明法の一浴染色織物は、発色性
、堅牢度共良好である。
As can be seen from the table, the monobath dyed fabric produced by the method of the present invention has good color development and fastness.

一方比較りフタの場合、100°C染色品はポリエステ
ル繊維の発色性が不十分で、かつ堅牢度性能も若干低い
。又これを7.30℃染色したものはボリエ表  ユ 洗濯堅牢度: JIS−L−Ogケ喧A−2法)ステル
繊維の発色性は十分なるものの、ペンベルブ繊維は染料
分解のため使用反応染料の色相とは全く異なるものとな
った。
On the other hand, in the case of the lid, the 100°C dyed product has insufficient color development of polyester fibers and also has slightly low fastness performance. In addition, this was dyed at 7.30℃ (Bollier table) Washing fastness: JIS-L-Og A-2 method) Although the color development of Stell fiber is sufficient, Penvelve fiber uses reactive dyes because the dye decomposes. The hue was completely different from that of .

実施例3 フェノール/テトラクロロエタンの、l//の混合溶媒
中で、3!f’cにおける固有粘度〔η〕(以下〔η〕
と表わす)が0.1.9のポリエチレンテレ7り■ノー
トを、紡糸温度302°Cで、孔径03古咽φ、孔数、
r+の紡糸口金より紡出し、糸条に平行方向の、22℃
の冷却風で冷却固化させた後、油剤を付与し6SoOV
分の速度で巻取った。得られた3 0d/l l/−f
のポリエチレンテレフタレ−1・繊維を、2’l!;”
Cに加熱した空気中でo、gs秒間、繊維に掛ける張力
を、39/d。
Example 3 In a mixed solvent of phenol/tetrachloroethane, 3! Intrinsic viscosity at f'c [η] (hereinafter [η]
A polyethylene telegraph with a diameter of 0.1.9 (represented as
Spun from an r+ spinneret, parallel to the yarn at 22°C.
After cooling and solidifying with cooling air, an oil agent is applied and 6SoOV
It was wound at a speed of 1 minute. Obtained 30d/l l/-f
2'l of polyethylene terephthalate fibers! ;”
The tension applied to the fiber for o, gs seconds in air heated to C is 39/d.

/ f/d 、 0.j f/dと変えて熱処理した。/ f/d, 0. j f/d was changed and heat treated.

これら熱処理した繊維および未処理繊維の(tanδ)
maxlTmayを表3に示した。
(tan δ) of these heat-treated fibers and untreated fibers
maxlTmay is shown in Table 3.

得られた4/種の繊維を実施例/と同様に編立て染色処
理し、仕上げした。これら編地の堅牢度およびベンペル
グ繊維部分の汚染度も表3に示した。
The obtained fibers of Type 4 were knitted, dyed and finished in the same manner as in Example. Table 3 also shows the fastness of these knitted fabrics and the degree of staining of the Bemperg fibers.

本発明法の範囲外である張力3グ/d処理系および未処
理系はいずれの染色温度でも堅牢度、ベンベルブ汚染性
が悪く、又/ 00 ’C染色ではポリエステル繊維部
分の発色が不十分であった。−力木発明法の範囲内にあ
る張力/2/dおよびθ31/d処理系はいずれの染色
温度においても発色性および堅牢衣    3 上段:染色温度ioo″C T段:  #   130℃ 度、汚染性が優れていた。
The 3 g/d tension treated system and the untreated system, which are outside the scope of the present invention, have poor fastness and benbel stain resistance at any dyeing temperature, and /00'C dyeing results in insufficient color development in the polyester fiber portion. there were. - The tension/2/d and θ31/d treatment systems within the range of the strength wood invention method have good color development and fastness at any dyeing temperature. It had excellent characteristics.

特許出願人 旭化成工業株式会社 代理人弁理士  星   野      透4Patent applicant: Asahi Kasei Industries, Ltd. Representative Patent Attorney Hoshi No Toru 4

Claims (1)

【特許請求の範囲】 (])、セルロース系m維とポリエステル繊維をそれぞ
れ少なくとも5・重量%以上含有する混用品を一浴で染
色するに際し、該ポリエステル繊維が、実質的にポリエ
チレンテレフタレートよりなり、測定周波数7/ OI
Iy、における力学的損失正接(−δ)のビーク高度(
T max )(’C)が105℃以下で、かっ幼iδ
のピーク値(:(tanδ)max 、)がo、tog
を越える構造特性・を有することを特徴とする混用品の
一浴・染色法。 (2)、ポリエステル繊維が、紡速qooom7g以上
で紡糸され1.2.2θ〜、:ioo’cの温度範囲内
で0/f/d以下の張力下で熱処理せしめたものである
′特許請求の範囲第1項記載の混用品の一浴染色法。
[Claims] (]) When dyeing a mixed product containing at least 5% by weight or more of cellulose m-fibers and polyester fibers in one bath, the polyester fibers substantially consist of polyethylene terephthalate, Measurement frequency 7/OI
The peak height (
T max )('C) is below 105℃,
The peak value (:(tanδ)max,) is o, tog
A single-bath dyeing method for mixed products characterized by having structural characteristics exceeding . (2) A polyester fiber is spun at a spinning speed of 7g or more and heat-treated under a tension of 0/f/d or less within a temperature range of 1.2.2θ to :ioo'c. A one-bath dyeing method for the mixed product according to item 1.
JP57173677A 1982-10-02 1982-10-02 Mono-bath dyeing of mixed article Pending JPS5966582A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57173677A JPS5966582A (en) 1982-10-02 1982-10-02 Mono-bath dyeing of mixed article

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57173677A JPS5966582A (en) 1982-10-02 1982-10-02 Mono-bath dyeing of mixed article

Publications (1)

Publication Number Publication Date
JPS5966582A true JPS5966582A (en) 1984-04-16

Family

ID=15965047

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57173677A Pending JPS5966582A (en) 1982-10-02 1982-10-02 Mono-bath dyeing of mixed article

Country Status (1)

Country Link
JP (1) JPS5966582A (en)

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