JPH0418071B2 - - Google Patents
Info
- Publication number
- JPH0418071B2 JPH0418071B2 JP60024088A JP2408885A JPH0418071B2 JP H0418071 B2 JPH0418071 B2 JP H0418071B2 JP 60024088 A JP60024088 A JP 60024088A JP 2408885 A JP2408885 A JP 2408885A JP H0418071 B2 JPH0418071 B2 JP H0418071B2
- Authority
- JP
- Japan
- Prior art keywords
- dyeing
- fiber
- wool
- weight
- solution
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 claims description 32
- 238000004043 dyeing Methods 0.000 claims description 26
- 239000000835 fiber Substances 0.000 claims description 17
- 229920003043 Cellulose fiber Polymers 0.000 claims description 15
- 239000000975 dye Substances 0.000 claims description 14
- 210000002268 wool Anatomy 0.000 claims description 14
- 239000000243 solution Substances 0.000 claims description 13
- 102000004169 proteins and genes Human genes 0.000 claims description 11
- 108090000623 proteins and genes Proteins 0.000 claims description 11
- 244000025254 Cannabis sativa Species 0.000 claims description 6
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 claims description 6
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 claims description 6
- 235000009120 camo Nutrition 0.000 claims description 6
- 235000005607 chanvre indien Nutrition 0.000 claims description 6
- 239000011487 hemp Substances 0.000 claims description 6
- 238000010025 steaming Methods 0.000 claims description 6
- 239000012670 alkaline solution Substances 0.000 claims description 5
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 235000019353 potassium silicate Nutrition 0.000 claims description 5
- 239000000985 reactive dye Substances 0.000 claims description 5
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
- 238000004804 winding Methods 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 229920000742 Cotton Polymers 0.000 description 10
- 239000000203 mixture Substances 0.000 description 8
- 238000005406 washing Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920000297 Rayon Polymers 0.000 description 6
- 239000002964 rayon Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004627 regenerated cellulose Substances 0.000 description 3
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 3
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 3
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 3
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000010014 continuous dyeing Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000009990 desizing Methods 0.000 description 2
- 229940061607 dibasic sodium phosphate Drugs 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 241001416177 Vicugna pacos Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- GTRGJJDVSJFNTE-UHFFFAOYSA-N chembl2009633 Chemical compound OC1=CC=C2C=C(S(O)(=O)=O)C=CC2=C1N=NC1=CC=CC=C1 GTRGJJDVSJFNTE-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- QKSIFUGZHOUETI-UHFFFAOYSA-N copper;azane Chemical compound N.N.N.N.[Cu+2] QKSIFUGZHOUETI-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010018 discharge printing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 for example Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000009981 jet dyeing Methods 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 210000000050 mohair Anatomy 0.000 description 1
- 229940045641 monobasic sodium phosphate Drugs 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- LIBWRRJGKWQFSD-UHFFFAOYSA-M sodium;2-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC=C1S([O-])(=O)=O LIBWRRJGKWQFSD-UHFFFAOYSA-M 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Coloring (AREA)
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はセルローズ系繊維と蛋白質系繊維とよ
りなる繊維構造物の染色方法に関するものであ
る。
(従来の技術)
従来セルローズ系繊維と羊毛等の蛋白質系繊維
の染色に関しては通常ウインス染色機又は液流染
色機によるバツチ染色が行われており、パツデイ
ング法では実施されていない。これはパツデイン
グ法では例えば再生繊維素繊維と羊毛とを均一に
染色することが困難であるからである。一方、綿
繊維構造物ではアルカリ性の染液を付与後ロール
アツプして染料を固着した後ソーピングする方法
が行なわれているが、羊毛等を含有する繊維構造
物には羊毛の染色性が問題があるため適用できな
い。
本発明考等はかかる欠陥のない染色方法を探究
の結果本発明を完成したものである。
(発明が解決しようとする問題点)
本発明の目的は均染性に優れしかも深みのある
色に染色しうるセルロース系繊維と蛋白質系繊維
とよりなる繊維構造物の染色法を提供するもので
ある。他の目的に斯かる染色をパツデイング法で
行なう染色方法を提供するにある。
(問題点を解決するための手段)
本発明方法はセルローズ系繊維と蛋白質系繊維
とよりなる繊維構造物を染色するに際し、ビニル
スルホン型反応性染料を含有する中性乃至酸性の
染液をパツデイング法にて付与後巻取つて放置し
た後乾燥し、次いでアルカリ溶液を付与後、蒸熱
処理することを特徴とする。
本発明に適用するセルローズ系繊維としてはビ
スコース法又は銅アンモニア法による再生繊維素
繊維、綿、麻等が挙げられるが再生繊維素繊維及
び麻が好ましく、再生繊維素繊維が特に好まし
い。
又蛋白質系繊維としては羊毛、アルパカ、モヘ
ーア、絹等が挙げられるが羊毛及び絹が好まし
い。
セルローズ系繊維と蛋白質系繊維との混合率は
通常セルローズ系繊維55〜90重量%、好ましくは
70〜85重量%と蛋白質系繊維10〜45重量%、好ま
しくは15〜30重量%である。両者の混合は混紡、
交撚、交織、交編のいずれでもよいが特に混紡が
好ましい。繊維構造物としては織物が特に好まし
い。
本発明に適用するビニルスルホン型反応性染料
は通常のものが使用され例えばヘキスト社のレマ
ゾール染料、住友化学(株)のスミフイツクス、三井
東圧(株)のセルマゾール、三菱化成(株)のダイラミラ
等が挙げられる。染液の濃度は特に限定すれば染
料の種類、色等により適宜決定すればよい。染液
のPHは中性乃至酸性に調整する必要があり、PH8
以下、好ましくは7以下、更に好ましくは6以
下、特に好ましくは5以下である。PHの調整は通
常酢酸ソーダ、ヘキサメタリン酸ソーダ或いは第
1リン酸ソーダ等で行なう。染液の温度は特に限
定されず通常の温度でよく、一般的には20〜30℃
でよい。
染液をパツデイング法で付与した繊維構造物は
一旦巻取り放置するが通常10〜60℃で放置する。
放置時間は温度により異なるが通常10〜50時間で
ある。好ましくは20〜30℃で20〜30時間放置す
る。この間に蛋白質系繊維がビニルスルホン型反
応性染料により染着される。
放置後繊維構造物を通常80℃以上、好ましくは
100〜120℃で乾燥し、アルカリ溶液、好ましくは
15〜25℃の40〜43度ボーメの水ガラス水溶液を付
与後、通常少なくとも100℃、好ましくは120〜
130℃の温度で蒸熱処理する。蒸熱処理時間は短
い方が好ましく高々1分程度である。
本発明の染色方法は一般に綿布帛に使用されて
いる連続染色機を適用することができる。
また、本発明の染色方法により染色した後、バ
ツト染料使いの抜染を行うこともできる。
(発明の効果)
本発明方法は通常の綿布帛の連続染色機を使用
して、均染性に優れしかも深みのある色を有する
繊維構造物が得られる。
また、低温染色と加熱短時間の染色であるた
め、省エネルギー、省水型の染色方法であると同
時に、染色された織物の風合も極めて良好であ
り、諸強力の低下も極めて低い水準である。
(実施例)
以下実施例で本発明を詳細に説明する。
実施例 1
レーヨン80重量%、羊毛20重量%の経糸30番単
糸(綿番手)経糸密度85本/吋、緯糸30番単糸
(綿番手)緯糸密度70本/吋の2/2綾組織で目
付165g/m2の混紡織物の無地染を下記の方法で
実施した。
上記混紡織物を80℃の湯で洗つた後、酵素糊抜
剤2g/を加えた60℃の湯で1時間処理し、充
分に湯洗し、脱水乾燥した。ビニルスルホン型反
応染料としてダイヤミラーレツドB(三菱化成(株)
製)40g/、スミフイツクス スカーレツトR
(住友化学(株)製)36g/、スミフイツクスブル
ーBB(住友化学(株)製)12g/を用い、尿素150
g/、ウール用均染剤ミグレガールWA−10
(日本染化(株)製)2g/、PH調節剤ヘキサメタ
リン酸ソーダ1g/、第1リン酸ソーダ2g/
、ニトロベンゼンスルホン酸ソーダ10g/、
酢酸10g/、アルギン酸ソーダ2.4g/より
成る無地染用染色液を作成し、上記混紡織物にピ
ツクアツプ率70%でパツデイングした後ロールア
ツプし30℃で24時間放置した。
放置後、120℃で乾燥し、40°ボーメの水ガラス
水溶液を常温でピツクアツプ率65%でパツドし、
100℃で1分間のスチーミングを行い、充分な湯
洗、水洗、脱水、乾燥して、均一なエンジ色のウ
ールライク風合のレーヨン、羊毛混紡無地染織物
を得た。
実施例1の無地染織物の染色堅牢度、引張り強
さ、引裂強さは後記第1表に示す。
実施例 2
レーヨン60重量%、絹40重量%の経糸30番単糸
(綿番手)経糸密度85本/吋、緯糸30番単糸(綿
番手)緯糸密度70本/吋のレーヨン、絹混紡織物
を下記の方法で染色した。
通常の方法で糊抜、精練した上記混紡織物にレ
マゾールブリリアントオレンジGD(ヘキスト(株)
製)60g/と、尿素100g/、絹均染剤ニツ
サンデイスパノールM−32A(日本油脂(株)製)2
g/、PH調節剤ヘキサメタリン酸ソーダ10g/
および第1リン酸ソーダ2g/、還元防止剤
ニトロベンベンスルホン酸ソーダ10g/、酢酸
10g/、アルギン酸ソーダ2.4g/より成る
染色溶液を、ピツクアツプ率70%でパデイングし
た後、ロールアツプして20℃で40時間放置した。
放置後120℃で乾燥した後、43°ボーメの水ガラス
水溶液をピツクアツプ率65%でパツドし、100℃、
1分間のスチーミングを行い、充分な湯洗、水
洗、乾燥を行つて、均染性に優れたオレンジ色の
シルクライクなレーヨン、絹混紡織物を得た。
実施例2の無地染織物の染色堅牢度、引張り強
さ、引裂強さを後記第1表に示す。
実施例 3
麻70重量%、羊毛30重量%の経糸30番単糸(綿
番手)経糸密度85本/吋、緯糸30番単糸(綿番
手)緯糸密度70本/吋の麻、羊毛混紡織物の染色
を下記の方法で実施した。
上記混紡織物を80℃の湯で洗つた後、酵素糊抜
剤2g/を加えた60℃の湯で1時間処理し、充
分に湯洗した。更に、トリポリリン酸ソーダ4
g/、精練漂白用活性剤サンデツトCKC−2
(三洋化成(株)製)2g/および過酸化水素15
g/より成る漂白浴で60℃、2時間の精練漂白
を行い、充分に湯洗、脱水、乾燥した。
染料としてレマゾール レツド3B(ヘキスト(株)
製)60g/を用いる外は、実施例1で用いたと
同様の染色液を作成し、上記麻、羊毛混紡織物に
ピツクアツプ率70%でパデイングし、ロールアツ
プして30℃で30時間放置した。放置後、120℃で
乾燥し、実施例1と同様に水ガラス水溶液をパツ
ド、スチーミング、湯洗、水洗、乾燥して、均染
性に優れた赤色の麻、羊毛混紡織物を得た。
実施例3の無地染織物の染色堅牢度、引張り強
さ、引裂き強さを後記第1表に示す。
【表】DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for dyeing a fibrous structure made of cellulose fibers and protein fibers. (Prior Art) Conventionally, cellulose fibers and protein fibers such as wool have been dyed in batches using a winch dyeing machine or jet dyeing machine, and have not been carried out by the pat dyeing method. This is because it is difficult to uniformly dye, for example, regenerated cellulose fibers and wool using the padding method. On the other hand, for cotton fiber structures, a method is used in which an alkaline dye solution is applied and then rolled up to fix the dye, followed by soaping. However, for fiber structures containing wool etc., there is a problem with the dyeability of wool. Therefore, it cannot be applied. The present inventors have completed the present invention as a result of searching for a dyeing method free of such defects. (Problems to be Solved by the Invention) An object of the present invention is to provide a method for dyeing a fiber structure made of cellulose fibers and protein fibers that has excellent level dyeing properties and can be dyed in deep colors. be. Another object of the present invention is to provide a dyeing method in which such dyeing is carried out by a padding method. (Means for Solving the Problems) When dyeing a fiber structure made of cellulose fibers and protein fibers, the method of the present invention involves dyeing a neutral to acidic dye solution containing a vinyl sulfone type reactive dye. It is characterized in that after being applied by a method, it is rolled up, left to stand, and then dried, then an alkaline solution is applied, and then a steaming treatment is performed. Examples of cellulose fibers to be used in the present invention include regenerated cellulose fibers produced by the viscose method or copper ammonia method, cotton, hemp, etc., with recycled cellulose fibers and hemp being preferred, and regenerated cellulose fibers being particularly preferred. Examples of protein fibers include wool, alpaca, mohair, and silk, with wool and silk being preferred. The mixing ratio of cellulose fiber and protein fiber is usually 55 to 90% by weight of cellulose fiber, preferably
70-85% by weight and protein fibers 10-45% by weight, preferably 15-30% by weight. A mixture of the two is a blend,
Any of mixed twisting, mixed weaving, and mixed knitting may be used, but mixed spinning is particularly preferred. A woven fabric is particularly preferred as the fibrous structure. Conventional vinyl sulfone type reactive dyes are used for the present invention, such as Remazol dye from Hoechst, Sumifix from Sumitomo Chemical Co., Selmazol from Mitsui Toatsu Co., Ltd., Dairamira from Mitsubishi Kasei Co., Ltd., etc. can be mentioned. The concentration of the dye solution may be determined as appropriate depending on the type of dye, color, etc., as long as it is not particularly limited. The PH of the dye solution must be adjusted to neutral or acidic, and should be adjusted to PH8.
Below, it is preferably 7 or less, more preferably 6 or less, particularly preferably 5 or less. The pH is usually adjusted using sodium acetate, sodium hexametaphosphate, dibasic sodium phosphate, or the like. The temperature of the dye solution is not particularly limited and may be any normal temperature, generally 20 to 30℃.
That's fine. The fibrous structure to which the dye solution has been applied by the padding method is once rolled up and left to stand, usually at 10 to 60°C.
The standing time varies depending on the temperature, but is usually 10 to 50 hours. Preferably, it is left to stand at 20-30°C for 20-30 hours. During this time, the protein fibers are dyed with a vinyl sulfone type reactive dye. After standing, the fiber structure is usually heated to 80℃ or higher, preferably
Dry at 100-120℃, alkaline solution, preferably
After applying a 40-43 degree Baume water glass aqueous solution at 15-25℃, usually at least 100℃, preferably 120-
Steam treatment at a temperature of 130℃. The shorter the steaming treatment time, the better, and it is about 1 minute at most. The dyeing method of the present invention can be applied to a continuous dyeing machine generally used for cotton fabrics. Further, after dyeing by the dyeing method of the present invention, discharge printing using a vat dye can also be performed. (Effects of the Invention) The method of the present invention uses a conventional continuous dyeing machine for cotton fabrics to obtain a fiber structure having excellent level dyeing properties and a deep color. In addition, because it is a low-temperature dyeing and short-time heating dyeing method, it is an energy- and water-saving dyeing method, and the texture of the dyed fabric is also extremely good, with an extremely low level of loss in strength. . (Example) The present invention will be explained in detail in the following example. Example 1 80% by weight of rayon, 20% by weight of wool, warp #30 single yarn (cotton count) warp density 85/inch, weft #30 single yarn (cotton count) weft density 70/inch 2/2 twill structure Plain dyeing of a blended fabric with a basis weight of 165 g/m 2 was carried out using the following method. After washing the blended fabric with hot water at 80°C, it was treated with hot water at 60°C containing 2 g of an enzyme desizing agent for 1 hour, thoroughly washed with hot water, and then dehydrated and dried. Diamirored B (Mitsubishi Kasei Corporation) as a vinyl sulfone type reactive dye
) 40g/Sumifits Scarlet R
(manufactured by Sumitomo Chemical Co., Ltd.) 36 g/, Sumifix Blue BB (manufactured by Sumitomo Chemical Co., Ltd.) 12 g/, urea 150
g/, wool leveling agent Migre Girl WA-10
(manufactured by Nippon Someka Co., Ltd.) 2g/, PH regulator sodium hexametaphosphate 1g/, dibasic sodium phosphate 2g/
, sodium nitrobenzene sulfonate 10g/,
A dyeing solution for plain dyeing consisting of 10 g of acetic acid and 2.4 g of sodium alginate was prepared and padded onto the above blended fabric at a pick-up rate of 70%, rolled up and left at 30°C for 24 hours. After leaving it to dry, it was dried at 120℃, and a 40℃ Baume water glass solution was padded at room temperature with a pick-up rate of 65%.
Steaming was performed at 100° C. for 1 minute, followed by sufficient hot water washing, water washing, dehydration, and drying to obtain a rayon/wool blend plain dyed fabric with a uniform dark red wool-like texture. The color fastness, tensile strength, and tear strength of the plain dyed fabric of Example 1 are shown in Table 1 below. Example 2 Rayon, silk blend fabric with 60% by weight rayon and 40% by weight silk, warp #30 single yarn (cotton count) warp density 85/inch, weft #30 single yarn (cotton count) weft density 70/inch was stained using the following method. Remazol Brilliant Orange GD (Hoechst Co., Ltd.)
(manufactured by Nippon Oil & Fats Co., Ltd.) 60g/, urea 100g/, silk leveling agent Nitsusan Dispanol M-32A (manufactured by Nippon Oil & Fats Co., Ltd.) 2
g/, PH regulator sodium hexametaphosphate 10g/
and monobasic sodium phosphate 2g/, reduction inhibitor nitrobenebensulfonic acid sodium 10g/, acetic acid
A dyeing solution consisting of 10 g/2.4 g of sodium alginate was padded at a pick-up ratio of 70%, then rolled up and left at 20° C. for 40 hours.
After being left to dry at 120°C, a 43° Baume water glass aqueous solution was applied at a pick-up rate of 65%, and the mixture was heated to 100°C.
Steaming was performed for 1 minute, followed by sufficient hot water washing, water washing, and drying to obtain an orange silk-like rayon/silk blended fabric with excellent level dyeing properties. The color fastness, tensile strength, and tear strength of the plain dyed fabric of Example 2 are shown in Table 1 below. Example 3 Hemp, wool blend fabric with 70% hemp and 30% wool by weight, warp #30 single yarn (cotton count) warp density 85/inch, weft #30 single yarn (cotton count) weft density 70/inch The staining was carried out using the following method. After washing the blended fabric with hot water at 80°C, it was treated with hot water at 60°C to which 2 g of an enzyme desizing agent had been added for 1 hour, and thoroughly washed in hot water. Furthermore, sodium tripolyphosphate 4
g/, activator for scouring bleaching Sandetto CKC-2
(manufactured by Sanyo Chemical Co., Ltd.) 2g/and hydrogen peroxide 15
Scouring and bleaching was carried out at 60°C for 2 hours in a bleach bath consisting of 500 g/ml, followed by thorough hot water washing, dehydration, and drying. Remazol Red 3B (Hoechst Co., Ltd.) as a dye
A dyeing solution similar to that used in Example 1 was prepared, except that 60 g/ml of the dyestuff was used, and the dye solution was padded onto the linen/wool blend fabric at a pick-up rate of 70%, rolled up, and left at 30° C. for 30 hours. After being left to stand, it was dried at 120°C, padded with an aqueous water glass solution, steamed, washed with hot water, washed with water, and dried in the same manner as in Example 1 to obtain a red hemp/wool blend fabric with excellent level dyeing properties. The color fastness, tensile strength, and tear strength of the plain dyed fabric of Example 3 are shown in Table 1 below. 【table】
Claims (1)
繊維構造物を染色するに際し、ビニルスルホン型
反応性染料を含有する中性乃至酸性の染液をパツ
デイング法にて付与後巻取つて放置した後乾燥
し、次いでアルカリ溶液を付与後蒸熱処理するこ
とを特徴とする繊維構造物の染色方法。 2 セルローズ系繊維が再生繊維素繊維又麻であ
る特許請求の範囲第1項記載の方法。 3 蛋白質系繊維が羊毛又は絹である特許請求の
範囲第1項記載の方法。 4 繊維構造物がセルローズ系繊維55〜90重量%
と蛋白質系繊維10〜45重量%とよりなる特許請求
の範囲第1項記載の方法。 5 巻取り後10〜30℃で放置する特許請求の範囲
第1項記載の方法。 6 放置時間が10〜50時間である特許請求の範囲
第1項記載の方法。 7 乾燥を80℃以上で行なう特許請求の範囲第1
項記載の方法。 8 アルカリ溶液が40〜43度ボーメの水ガラス水
溶液である特許請求の範囲第1項記載の方法。 9 蒸熱処理を少なくとも100℃で行なう特許請
求の範囲第1項記載の方法。 10 アルカリ溶液付与前に予備蒸熱処理を行な
う特許請求の範囲第1項記載の方法。[Scope of Claims] 1. When dyeing a fibrous structure made of cellulose fibers and protein fibers, a neutral to acidic dye solution containing a vinyl sulfone type reactive dye is applied by a patting method and then rolled up. 1. A method for dyeing a fibrous structure, which comprises: drying after being left to stand, then applying an alkaline solution and then subjecting it to a steam treatment. 2. The method according to claim 1, wherein the cellulose fiber is recycled cellulose fiber or hemp. 3. The method according to claim 1, wherein the protein fiber is wool or silk. 4 Fiber structure is 55-90% by weight of cellulose fibers
and 10 to 45% by weight of protein fiber. 5. The method according to claim 1, wherein the method is left at 10 to 30°C after winding. 6. The method according to claim 1, wherein the standing time is 10 to 50 hours. 7 Claim 1 in which drying is carried out at 80°C or higher
The method described in section. 8. The method according to claim 1, wherein the alkaline solution is a water glass aqueous solution having a temperature of 40 to 43 degrees Baumé. 9. The method according to claim 1, wherein the steaming treatment is carried out at a temperature of at least 100°C. 10. The method according to claim 1, wherein a preliminary steaming treatment is performed before applying the alkaline solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60024088A JPS61186580A (en) | 1985-02-08 | 1985-02-08 | Dyeing of fiber structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60024088A JPS61186580A (en) | 1985-02-08 | 1985-02-08 | Dyeing of fiber structure |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61186580A JPS61186580A (en) | 1986-08-20 |
JPH0418071B2 true JPH0418071B2 (en) | 1992-03-26 |
Family
ID=12128635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60024088A Granted JPS61186580A (en) | 1985-02-08 | 1985-02-08 | Dyeing of fiber structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61186580A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2731091B2 (en) * | 1992-08-10 | 1998-03-25 | 日清紡績株式会社 | Method for thickening cellulosic fiber structure |
JP4743389B2 (en) * | 2005-04-27 | 2011-08-10 | 株式会社吉野工業所 | Small discharge container |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5637381A (en) * | 1979-08-17 | 1981-04-11 | Bayer Ag | Dyeing of wool cellulose fiber blend |
-
1985
- 1985-02-08 JP JP60024088A patent/JPS61186580A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5637381A (en) * | 1979-08-17 | 1981-04-11 | Bayer Ag | Dyeing of wool cellulose fiber blend |
Also Published As
Publication number | Publication date |
---|---|
JPS61186580A (en) | 1986-08-20 |
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