JPS61119784A - Dyeing of fiber structure - Google Patents

Dyeing of fiber structure

Info

Publication number
JPS61119784A
JPS61119784A JP59237069A JP23706984A JPS61119784A JP S61119784 A JPS61119784 A JP S61119784A JP 59237069 A JP59237069 A JP 59237069A JP 23706984 A JP23706984 A JP 23706984A JP S61119784 A JPS61119784 A JP S61119784A
Authority
JP
Japan
Prior art keywords
dyeing
aqueous solution
wool
fiber structure
dyed
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.)
Granted
Application number
JP59237069A
Other languages
Japanese (ja)
Other versions
JPH0453989B2 (en
Inventor
大隈 茂
原 正美
大森 義次
岡嶋 世志彦
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.)
Kanebo Rayon Ltd
Kanebo Ltd
Original Assignee
Kanebo Rayon Ltd
Kanebo Ltd
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 Kanebo Rayon Ltd, Kanebo Ltd filed Critical Kanebo Rayon Ltd
Priority to JP59237069A priority Critical patent/JPS61119784A/en
Publication of JPS61119784A publication Critical patent/JPS61119784A/en
Publication of JPH0453989B2 publication Critical patent/JPH0453989B2/ja
Granted legal-status Critical Current

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  • Coloring (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

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】 (産業上の利用分野) この発明は、再生繊維素繊維と羊毛とよりなる繊維構造
物の染色法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for dyeing a fiber structure made of recycled cellulose fibers and wool.

(従来技術) 再生繊維素繊維と羊毛とよりなるuA維槽構造物、反応
染料で染色するに際し、ウールを保護する酸性領域のp
■、たとえばp■6で染色すると、羊毛は染まるが、再
生繊維素繊維は染まらない欠点がある。又再生繊維素繊
維は、通常アルカリ性で反応染料による染色が行なわれ
ているが、通常の染色法で、前記繊維構造物を染色する
とウールが染まり難<、これまた同色に染まらない欠点
がある。
(Prior art) uA fibrous structure made of regenerated cellulose fibers and wool;
(2) For example, when dyeing with p (6), wool is dyed, but recycled cellulose fibers are not dyed. In addition, recycled cellulose fibers are usually dyed with alkaline reactive dyes, but when the fiber structure is dyed using a normal dyeing method, wool is difficult to dye and also has the disadvantage that it cannot be dyed to the same color.

特に黒、濃紺、濃赤等の濃色に染色するに際し、反応染
料による一浴同時染色は困難とされ、これら再生繊維素
繊維とウールよりなる繊維構造物の染色は、−浴二段法
又は二浴染色法が必要とされている。
In particular, when dyeing dark colors such as black, dark blue, and dark red, simultaneous dyeing in one bath with reactive dyes is considered difficult, and the dyeing of fiber structures made of recycled cellulose fibers and wool is carried out by - two-bath method or A two-bath dyeing method is needed.

(発明が解決しようとする問題点) 再生繊維素繊維と羊毛とよりなる繊維構造物を染色する
に際し、−浴二段、二浴染色法は、操作が煩雑であり、
染色コストの上昇をもたらす。−万一浴同時染色法は、
染色コストの低減をもたらすが、黒、濃紺、濃赤等の濃
色に染色する際、染まらない欠点がある。本発明の目的
は、前記繊維構造物の一浴同時染色法の提供にある。
(Problems to be Solved by the Invention) When dyeing a fiber structure made of recycled cellulose fibers and wool, the two-bath and two-bath dyeing methods are complicated in operation;
This results in an increase in dyeing costs. -In the unlikely event that the bath simultaneous staining method is
Although it reduces dyeing costs, it has the disadvantage that it cannot be dyed in deep colors such as black, dark blue, and dark red. An object of the present invention is to provide a method for simultaneous dyeing of the fiber structure in one bath.

(問題点を解決するための手段) 本発明方法は、再生繊維素繊維と羊毛とよりなる繊維構
造物を染色するに際し、pFI 9〜11゜好ましくは
pH9〜10のアルカリ性水溶液で前処理し、前記繊維
構造物のN/1ONaOH71(溶液に対する溶解度を
1〜4%好ましくは1〜2%及びバイμVり法吸水性を
10〜181、好ましくは11〜12cW4とせしめた
後、染色することを特徴とする。本発明に適用される再
生1a細素繊維としては、ビスコース法レーヨン、銅ア
ンモニア法レーヨンのいずれでも差し支えない。再生繊
維素繊維と羊毛よりなる繊維構造物は、これらの混紡糸
及びそれよりなる織編物又は再生繊維素繊維よりなる糸
条と羊毛糸との交撚糸、交織織物、交編編物等が挙げら
れる。再生w4維素繊維と羊毛との混合割合は、通常再
生繊維素繊細50〜97%、羊毛50〜8%であり、好
ましくは再生繊維素繊維70〜95%、羊毛80〜6%
である。
(Means for Solving the Problems) The method of the present invention involves pre-treating with an alkaline aqueous solution having a pFI of 9 to 11 degrees, preferably a pH of 9 to 10, when dyeing a fiber structure made of recycled cellulose fibers and wool. The fiber structure is dyed after the solubility in N/1ONaOH71 (solubility in solution is 1 to 4%, preferably 1 to 2%) and biμV water absorption is 10 to 181, preferably 11 to 12 cW4. The recycled 1a fine filament applied to the present invention may be either viscose process rayon or copper ammonia process rayon.The fiber structure made of recycled cellulose fiber and wool can be made of these blended yarns and Examples include woven and knitted fabrics made of the same, intertwisted yarns of yarns made of recycled cellulose fibers and wool yarn, interwoven fabrics, interwoven knitted fabrics, etc. The mixing ratio of recycled W4 cellulose fibers and wool is usually 50-97% fine, 50-8% wool, preferably 70-95% recycled cellulose fiber, 80-6% wool.
It is.

さらに本発明において、使用されるアルカリ性水溶液と
は、水酸化ナトリウム、炭酸ナトリウム、リン酸ナトリ
ウム又はアンモニアの水溶液が挙げられ、単独あるいは
混合して使用される。又過酸化水素と共存して使用する
こともできる。アルカリ性水溶液のpHは9〜11好ま
しくは9〜10に調整し、温度は通常60〜95°C1
好ましくは60〜80℃で、80〜60分温揚中で処理
する。
Furthermore, in the present invention, examples of the alkaline aqueous solution used include aqueous solutions of sodium hydroxide, sodium carbonate, sodium phosphate, or ammonia, which may be used alone or in combination. It can also be used in combination with hydrogen peroxide. The pH of the alkaline aqueous solution is adjusted to 9-11, preferably 9-10, and the temperature is usually 60-95°C.
It is preferably heated at 60 to 80°C for 80 to 60 minutes.

共存する過酸化水素の濃度はO〜50 g/l好ましく
は10 g71以下が良い。処理方法として、コールド
バッチ方式でも良い。
The concentration of coexisting hydrogen peroxide is O to 50 g/l, preferably 10 g/l or less. As a processing method, a cold batch method may be used.

前処理された繊維構造物は、染色により着色するのであ
るが、セルロース用反応染料、直接染粍スレン染料を用
いることができ、その方法としては、吸尽法、パッディ
ング法、コールドパッチ法等の適用が可能であり、通常
行なわれている繊維素繊維の染色法がそのまま使用でき
る。
The pretreated fiber structure is colored by dyeing, and reactive dyes for cellulose and direct dyeing thren dyes can be used, and methods include exhaustion method, padding method, cold patch method, etc. can be applied, and the commonly used dyeing method for cellulose fibers can be used as is.

一般的に、pET8〜9未満のアルカリ水溶液で前処理
すると、羊毛の脆化は少ないが、このpH範囲で染色し
た場合同色性を示さない。
Generally, when pre-treated with an alkaline aqueous solution having a pET of less than 8-9, the wool becomes less brittle, but when dyed in this pH range, it does not show the same color.

pH11を越えるアルカリ性水溶液で前処理し染色した
場合、同色性を示すが、羊毛の脆化が進み、風合の硬化
が顕著である。
When the wool is pretreated and dyed with an alkaline aqueous solution with a pH exceeding 11, it exhibits the same color property, but the wool becomes brittle and its texture becomes noticeably hardened.

前処理時のアルカリ性水溶液のp’EIと温度の組み合
わせで、風合が種々変化することは、当然のことである
が、前処理された繊維構造物のN/1ONaOHfII
解度が1〜4%好ましくは1〜2%及びパイシック法吸
水性が10〜181、好ましくは11〜12clIであ
ることが、同色性及び風合が良好となる範囲なのである
It goes without saying that the texture changes in various ways depending on the combination of p'EI of the alkaline aqueous solution and temperature during pretreatment, but the N/1ONaOHfII of the pretreated fiber structure
The solubility is 1 to 4%, preferably 1 to 2%, and the pisic method water absorption is 10 to 181, preferably 11 to 12clI, in which the same color property and hand feel are good.

(発明の効果) 本発明は、淡色、中色のみならず、これまで同色に染ま
らない欠点があった黒、濃紺、濃赤等の濃色でも一般的
に使用されている染色法で、同時染色が可能であり、羊
毛の脆化も少なく風合も良好である。
(Effect of the invention) The present invention is a dyeing method that is commonly used not only for light colors and medium colors, but also for dark colors such as black, dark blue, and dark red, which had the disadvantage of not being dyed in the same color. It can be dyed, has less brittleness, and has a good texture.

このような効果は、特定条件下でのアルカリ性水溶液で
処理し、N/1ONaOH水溶液に対する溶解度を1〜
4%、好ましくは1〜2%及びバイシック法吸水性を1
0〜18個、好ましくは11〜12αとせしめた繊維構
造物を着色することによりはじめて得られるものであり
、その工業的利用価値は大きい。
Such an effect can be obtained by treating with an alkaline aqueous solution under specific conditions and increasing the solubility in an N/1ONaOH aqueous solution from 1 to 1.
4%, preferably 1-2% and bisic method water absorption of 1
It can only be obtained by coloring a fiber structure with 0 to 18 α, preferably 11 to 12α, and its industrial utility value is great.

(実施例) 以下実施例を挙げて本発明を具体的に説明する。(Example) The present invention will be specifically explained below with reference to Examples.

な招、実施例記載の強力、白色度、アルカリ溶解度、吸
水性、染色性、風合は、下記の方法にて測定した。
In addition, strength, whiteness, alkali solubility, water absorption, dyeability, and texture described in the examples were measured by the following methods.

(1)  強力(g) 布帛からたて及びよこの糸を取り出し、テンシロンにて
糸強力を測定した。
(1) Tenacity (g) Warp and weft yarns were taken out from the fabric, and the yarn tenacity was measured using a Tensilon.

(2)  白色度(至) 積分球による反射光測定装置の附属した分光光度計を用
いて、波長400闘にて酸化マグネシウムに対する反射
率%を測定し、白さの指標とした。
(2) Whiteness (total) Using a spectrophotometer attached to a reflected light measuring device using an integrating sphere, the reflectance % with respect to magnesium oxide was measured at a wavelength of 400 cm, and was used as an index of whiteness.

(3)  アルカリ溶解度% N/1ONaOH溶液100倍量を使用し、65°Cに
て1時間処理し、処理前後の重量減少率を溶解度とした
(3) Alkali Solubility % Using 100 times the amount of N/1ONaOH solution, the solution was treated at 65°C for 1 hour, and the weight loss rate before and after the treatment was taken as the solubility.

(4)吸水性− JILT、 1096吸水速度(バイシック法)の測定
値をもって吸水性能とした。
(4) Water absorbency - The measured value of JILT, 1096 water absorption rate (Bisic method) was defined as water absorption performance.

(5)染色性 染色布の霜ぶり調の有無を目視判定した。(5) Stainability The presence or absence of a frosty tone on the dyed fabric was visually determined.

(6)風合 糊抜布の風合を5とし、梢々硬化4、少し硬化8、可成
り硬化2、硬化大1として平均値で表示した。
(6) Texture The texture of the starched fabric was set as 5, and was expressed as an average value, with 4 being slightly hard, 8 being slightly hard, 2 being quite hard, and 1 being very hard.

(実施例1) 線条工程にて、混紡率レーヨン80、羊毛20になるよ
うに混紡した後、紡績して808とし、これを緯糸に、
レーヨン808を経糸に、密度経100、緯72本/吋
の綾織物を製織した。
(Example 1) In the filament process, after blending so that the blend ratio is rayon 80 and wool 20, it is spun to 808, and this is used as a weft.
A twill fabric with a warp density of 100 and a weft of 72 threads/inch was woven using rayon 808 as the warp.

この織物を酵素糊抜剤によって糊抜を行ない、pT(9
,5及びI)H11のノニオン界面活性剤を含む炭酸ナ
トリウム水溶液にて、浴比1:80、i度80°Cで8
0分間前処理し、水洗後105°C熱風下にて乾燥した
This fabric was desized using an enzyme desizing agent, pT (9
, 5 and I) H11 in a sodium carbonate aqueous solution containing a nonionic surfactant at a bath ratio of 1:80 and a temperature of 80°C.
The sample was pretreated for 0 minutes, washed with water, and then dried under hot air at 105°C.

次いで](emajol Black B 6%owt
 、 RemajolBrilliant yello
w QB 4%owt、 HemajolQrange
 8R8%owt1芒硝50 g/l、炭酸ナトリウム
20 g/lを用いて、浴比1:80にて、60°Cで
60分染色を行ない、良好な黒染品を得た。比較例1は
、前処理しないもの(糊抜布)、比較例2は前処理時の
水溶液の1)F(を12.0とし、その他の条件は本発
明例1と全く同じである。
Next] (emajol Black B 6%owt
, RemajolBrilliant yellow
w QB 4%owt, HemajolQrange
Dyeing was carried out at 60°C for 60 minutes using 50 g/l of 8R8%owt1 Glauber's salt and 20 g/l of sodium carbonate at a bath ratio of 1:80 to obtain a good black dyed product. In Comparative Example 1, no pretreatment was performed (desizing cloth), in Comparative Example 2, 1)F(1) of the aqueous solution during pretreatment was set to 12.0, and other conditions were exactly the same as Example 1 of the present invention.

結果を第1表に示す。The results are shown in Table 1.

第  1  表 上記比較例1は、糊抜した布であるが、染色したものは
、霜ふり調であった。比較例2は、霜ふシ調を改善した
ものの、強力低下が大きく、風合の硬化も認められ、羊
毛の脆化が進んで好ましくない。
Table 1 Comparative Example 1 above was a starched cloth, but the dyed cloth had a frosty texture. In Comparative Example 2, although the frost-like appearance was improved, the strength was greatly reduced, the hand was hardened, and the wool became brittle, which is not preferable.

本発明例1及び2は、霜ふシ調を改善した良好な黒染品
が得られ、しかも強力の低下が少なく、風合の硬化も少
なかった。
In Examples 1 and 2 of the present invention, good black-dyed products with improved frost appearance were obtained, and there was little decrease in strength and hardening of hand.

(実施例2) レーヨン808を&l糸K、レーヨン80、羊毛20の
混紡糸808を緯糸に、密度経100、緯72(本/吋
)の平組織織物を、酵素糊抜剤によって糊抜を行ない、
過酸化水素(85%品)11/A’。
(Example 2) A plain weave fabric with a density of 100 and a weft of 72 (thin/inch), using rayon 808 &l yarn K, rayon 80, and wool 20 blended yarn 808 as the weft, was desized using an enzyme desizing agent. ,
Hydrogen peroxide (85% product) 11/A'.

ノニオン界面活性剤1 f/lを含む炭酸ナトリウム水
溶液にて、1) E[9,5、温度80℃で80分間前
処理し、水洗後105℃熱風下にて乾燥した0次いでx
ayacion yellow E−8N4G  6%
owt 。
Pretreated with an aqueous sodium carbonate solution containing 1 f/l of a nonionic surfactant, 1) E[9,5, at a temperature of 80°C for 80 minutes, washed with water and dried under hot air at 105°C.
ayacion yellow E-8N4G 6%
owt.

Kayacion HaQ n−8NG 6%owt 
、 xayac 1onBed A−8B  1%ow
tの処決で、実施例1と同様に染色を行ない、濃紺の染
色物を得た・比較例1は、前処理時の水溶液のI)Hを
8.6、比較例2は、I)Hな12.0とし、その他の
条件は本発明例1と全く同じである。結果を第2表に示
すO 第  2  表 上記比較例1では、白色度良好なものの、染色したもの
は霜ふり調であった。比較例2では、霜ふシ調を改善し
たものの、強力低下が大きく、風合の硬化も認められ、
羊毛の脆化が進んで好ましくない。
Kayacion HaQ n-8NG 6%owt
, xayac 1onBed A-8B 1%ow
Dyeing was carried out in the same manner as in Example 1 to obtain a dark blue dyed product.Comparative Example 1 had an I)H of 8.6 in the aqueous solution during pretreatment, and Comparative Example 2 had an I)H of 8.6. The other conditions were exactly the same as in Example 1 of the present invention. The results are shown in Table 2.Table 2 Although the above Comparative Example 1 had good whiteness, the dyed product had a frosty tone. In Comparative Example 2, although the frost texture was improved, there was a significant decrease in strength and hardening of the texture was observed.
This is undesirable because the wool becomes brittle.

本発明例1は、霜ふυ詞を改善し、しかも強力の低下が
少なく、風合の硬化も少なかった。
Inventive Example 1 had improved frost resistance, less decrease in strength, and less hardening of hand.

(実施例8) レーヨン80、羊毛20の混紡糸208を、経、緯糸に
密度経67、緯62(本/吋)の綾織物を、酵素糊抜剤
によって糊抜を行ない、過酸化水素(86%品) 10
 Vl 、 / =オフ界Wif&性剤1t/lを含む
炭酸ナトリウム水溶液にて、pHl010、温度80℃
で80分間処理し、水洗後105℃熱風下にて乾燥した
。次いで、実施例1と同様に染色を行ない、良好な黒染
品を得た。比較例1は、前処理しないもの(糊抜布)、
比較例21d、前処理時の水溶液のpHを8.0とし、
その他の条件は、本発明例1と全く同じである。
(Example 8) A twill fabric made of a blended yarn 208 of rayon 80 and wool 20, with a warp and weft density of 67 and 62 threads/inch, was desized using an enzyme desizing agent, and hydrogen peroxide (86 % product) 10
Vl, / = off-world Wif & sex agent 1t/l in sodium carbonate aqueous solution, pHl010, temperature 80°C
The sample was treated for 80 minutes, washed with water, and then dried under hot air at 105°C. Next, dyeing was carried out in the same manner as in Example 1, and a good black-dyed product was obtained. Comparative Example 1 is one without pre-treatment (sizing cloth),
Comparative Example 21d, the pH of the aqueous solution during pretreatment was 8.0,
The other conditions were exactly the same as those in Inventive Example 1.

結果を第8表に示す。The results are shown in Table 8.

第  8  表 上記比較例1では、糊抜布を染色したものであるが、霜
ふシ調となった。比較例2では、霜ふ如調を稍々改善し
たものの、風合が粗硬となった。
Table 8 In Comparative Example 1 above, the starched fabric was dyed, and the result was a frosty texture. In Comparative Example 2, although the frost texture was slightly improved, the texture became rough and hard.

本発明例1は、霜ふシ調を改善し、しかも強力の低下も
、風合の硬化も少なかった。
Inventive Example 1 improved the frost-like appearance, and there was also little decrease in strength and hardening of the texture.

(実施例4) 実施例2と同様の条件で、製織、糊抜、或は更に前処理
した生地を、Kayac i on Red E−8B
N501/l、Na0H(88°B ” ) 5 cc
/1 、尿素100y/1. yixer RC−FD
 (ヘキスト社製)  100t/lを含む染液をパッ
ドし、ロール巻きした後水分の蒸発を防止して、25℃
で15時間放置した後・洗浄し乾燥して美麗な赤色染色
物を得た。
(Example 4) Weaving, desizing, or further pretreatment under the same conditions as in Example 2 was carried out using Kayacion Red E-8B.
N501/l, Na0H (88°B”) 5 cc
/1, urea 100y/1. yixer RC-FD
(manufactured by Hoechst) After padding with a dye solution containing 100 t/l and rolling it, prevent moisture evaporation and dry at 25°C.
After leaving it for 15 hours, washing and drying, a beautiful red dyed product was obtained.

結果を第4表に示す。The results are shown in Table 4.

第  4  表 上記比較例1では、霜ふシ調で不満足のものであった。Table 4 Comparative Example 1 had an unsatisfactory frosty appearance.

比較例2では、霜ふり詞を改善したものの、強力低下が
大きく、風合の硬化も大きかった。
In Comparative Example 2, although the frosting was improved, the strength was significantly lowered and the texture was also significantly hardened.

本発明例1では、霜ふり調を改善し、しかも強力の低下
も少なく、風合の硬化も少なかった。
In Example 1 of the present invention, the frosting texture was improved, and there was little decrease in strength, and there was little hardening of the texture.

(実施例5) 実施例1の綾織物を、酵素糊抜剤によシ糊抜を行ない、
H2O2(85%品)10f/l、ラスタビルに109
5(ヘキスト社製、アニオン界面活性剤)7 t/l、
 pHt oを含む前処理液をパッドし、ロ−ル巻きに
した後、水分の蒸発を防止して、25℃で16時間放置
した後水洗乾燥した0次いで実施例4と同様に染色を行
ない、美麗な赤色染色物を得九〇 比較例1は、前処理しないもの(糊抜布)、比較例2は
、前処理液のpHを8.0とし、その他の条件は本発明
例1と全く同じである。比較例においては不満足な結果
を得た。
(Example 5) The twill fabric of Example 1 was desized using an enzyme desizing agent,
H2O2 (85% product) 10f/l, 109 in Rasta Building
5 (manufactured by Hoechst, anionic surfactant) 7 t/l,
After padding with a pre-treatment solution containing pH 0 and winding it into a roll, preventing moisture evaporation, leaving it for 16 hours at 25°C, washing with water and drying. A beautiful red dyed product was obtained.90 Comparative Example 1 is without pre-treatment (desizing cloth), Comparative Example 2 is that the pH of the pre-treatment liquid is 8.0, and the other conditions are exactly the same as Inventive Example 1. It's the same. In the comparative example, unsatisfactory results were obtained.

結果を第5表に示す。The results are shown in Table 5.

第  5  表 (実施例6) 実施例1と同様の条件で、製織、糊抜或は更に前処理し
゛た生地を、n1rect past Black B
1605%OWt、芒硝10%owt浴比1:80にて
80℃で60分染色を行ない、良好な黒染品を得た。
Table 5 (Example 6) Weaving, desizing, or further pre-treatment of the fabric under the same conditions as in Example 1 was performed using n1rect past Black B.
Dyeing was carried out at 80° C. for 60 minutes at a bath ratio of 1:80 of 1605% OWt and 10% Glauber's salt to obtain a good black dyed product.

結果を第6表に示す。The results are shown in Table 6.

第  6  表 上記比較例1は、糊抜した布であるが、染色したものは
霜ふり調であった。比較例2は、霜ふp調を改善したも
のの強力低下が大きく、風合の硬化も認められ、羊毛の
脆化が進んで好ましくない。
Table 6 Comparative Example 1 above was a starched cloth, but the dyed cloth had a frosty texture. In Comparative Example 2, although the frost and pep tone was improved, the strength was greatly reduced, hardening of the hand was observed, and the wool became brittle, which is not preferable.

本発明例1及び2は、霜ふυ詞を改善した良好な黒染品
が得られ、しかも強力の低下が少なく、風合の硬化も少
なかった。
In Examples 1 and 2 of the present invention, good black-dyed products with improved frosting were obtained, and there was little decrease in strength and hardening of hand.

Claims (7)

【特許請求の範囲】[Claims] (1)再生繊維素繊維と羊毛とよりなる繊維構造物を染
色するに際し、pH9〜11のアルカリ性水溶液で前処
理し、前記繊維構造物の 1/10N・NaOH水溶液に対する溶解度を1〜4%
及びバイレック法吸水性を10〜13cmとせしめた後
、染色することを特徴とする繊維構造物の染色法。
(1) When dyeing a fibrous structure made of recycled cellulose fibers and wool, pre-treat with an alkaline aqueous solution of pH 9 to 11 to reduce the solubility of the fibrous structure in a 1/10N NaOH aqueous solution to 1 to 4%.
and Byrek method: A method for dyeing a fiber structure, which comprises dyeing after making the water absorbency 10 to 13 cm.
(2)再生繊維素繊維がビスコース繊維である特許請求
の範囲第1項記載の染色法。
(2) The dyeing method according to claim 1, wherein the regenerated cellulose fibers are viscose fibers.
(3)繊維構造物が糸、織物又は編物である特許請求の
範囲第1項記載の染色法。
(3) The dyeing method according to claim 1, wherein the fiber structure is a yarn, a woven fabric, or a knitted fabric.
(4)繊維構造物が再生繊維素繊維50〜97%、羊毛
50〜8%よりなる特許請求の範囲第1項記載の染色法
(4) The dyeing method according to claim 1, wherein the fiber structure consists of 50 to 97% recycled cellulose fibers and 50 to 8% wool.
(5)アルカリ性水溶液が水酸化ナトリウム、炭酸ナト
リウム、リン酸ナトリウム又はアンモニアの水溶液ある
いは過酸化水素を共存する水溶液である特許請求の範囲
第1項記載の染色法。
(5) The dyeing method according to claim 1, wherein the alkaline aqueous solution is an aqueous solution of sodium hydroxide, sodium carbonate, sodium phosphate, or ammonia, or an aqueous solution containing hydrogen peroxide.
(6)染色を反応染料で行なう特許請求の範囲第1項記
載の染色法。
(6) The dyeing method according to claim 1, wherein dyeing is carried out using a reactive dye.
(7)染色を直接染料で行なう特許請求の範囲第1項記
載の染色法。
(7) The dyeing method according to claim 1, wherein dyeing is carried out using a direct dye.
JP59237069A 1984-11-10 1984-11-10 Dyeing of fiber structure Granted JPS61119784A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59237069A JPS61119784A (en) 1984-11-10 1984-11-10 Dyeing of fiber structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59237069A JPS61119784A (en) 1984-11-10 1984-11-10 Dyeing of fiber structure

Publications (2)

Publication Number Publication Date
JPS61119784A true JPS61119784A (en) 1986-06-06
JPH0453989B2 JPH0453989B2 (en) 1992-08-28

Family

ID=17009953

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59237069A Granted JPS61119784A (en) 1984-11-10 1984-11-10 Dyeing of fiber structure

Country Status (1)

Country Link
JP (1) JPS61119784A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005314845A (en) * 2004-04-30 2005-11-10 Seiren Co Ltd Inkjet printing cloth and method for producing the same
JP2008240175A (en) * 2007-03-26 2008-10-09 National Institute Of Advanced Industrial & Technology Method for photo-modifying regenerated fiber and apparatus therefor
CN103643563A (en) * 2013-11-30 2014-03-19 江苏金泰针织有限责任公司 Dyeing and finishing process for protein fiber-containing blended knitted fabric

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005314845A (en) * 2004-04-30 2005-11-10 Seiren Co Ltd Inkjet printing cloth and method for producing the same
JP2008240175A (en) * 2007-03-26 2008-10-09 National Institute Of Advanced Industrial & Technology Method for photo-modifying regenerated fiber and apparatus therefor
CN103643563A (en) * 2013-11-30 2014-03-19 江苏金泰针织有限责任公司 Dyeing and finishing process for protein fiber-containing blended knitted fabric

Also Published As

Publication number Publication date
JPH0453989B2 (en) 1992-08-28

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