JPH0418070B2 - - Google Patents
Info
- Publication number
- JPH0418070B2 JPH0418070B2 JP59230922A JP23092284A JPH0418070B2 JP H0418070 B2 JPH0418070 B2 JP H0418070B2 JP 59230922 A JP59230922 A JP 59230922A JP 23092284 A JP23092284 A JP 23092284A JP H0418070 B2 JPH0418070 B2 JP H0418070B2
- Authority
- JP
- Japan
- Prior art keywords
- dyeing
- dye
- acid
- integer
- aliphatic monocarboxylic
- 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
- 238000004043 dyeing Methods 0.000 claims description 35
- -1 oxyalkylene ether Chemical compound 0.000 claims description 12
- 229920000728 polyester Polymers 0.000 claims description 8
- 239000000835 fiber Substances 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 150000005846 sugar alcohols Polymers 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003945 anionic surfactant Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 125000006353 oxyethylene group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 239000002253 acid Substances 0.000 description 6
- 238000005187 foaming Methods 0.000 description 6
- 239000000986 disperse dye Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 241000083869 Polyommatus dorylas Species 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- YXZRCLVVNRLPTP-UHFFFAOYSA-J turquoise blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Cu+2].NC1=NC(Cl)=NC(NC=2C=C(NS(=O)(=O)C3=CC=4C(=C5NC=4NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)NC=4NC(=C6C=C(C=CC6=4)S([O-])(=O)=O)NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)N5)C=C3)C(=CC=2)S([O-])(=O)=O)=N1 YXZRCLVVNRLPTP-UHFFFAOYSA-J 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- HZUBBVGKQQJUME-UHFFFAOYSA-N 1,5-diamino-2-bromo-4,8-dihydroxyanthracene-9,10-dione Chemical compound O=C1C2=C(N)C(Br)=CC(O)=C2C(=O)C2=C1C(O)=CC=C2N HZUBBVGKQQJUME-UHFFFAOYSA-N 0.000 description 1
- VDPWYLLVHRYGOQ-UHFFFAOYSA-N 7-ethyloctadecane Chemical compound CCCCCCCCCCCC(CC)CCCCCC VDPWYLLVHRYGOQ-UHFFFAOYSA-N 0.000 description 1
- BLMUTSBGJBEFFR-UHFFFAOYSA-N 7-ethyltetradecane Chemical compound CCCCCCCC(CC)CCCCCC BLMUTSBGJBEFFR-UHFFFAOYSA-N 0.000 description 1
- SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 1
- CWEKGCILYDRKNV-KPOOZVEVSA-L Orange B Chemical compound [Na+].[Na+].CCOC(=O)c1[nH]n(-c2ccc(cc2)S([O-])(=O)=O)c(=O)c1\N=N\c1ccc(c2ccccc12)S([O-])(=O)=O CWEKGCILYDRKNV-KPOOZVEVSA-L 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009981 jet dyeing Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000013987 orange B Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Landscapes
- Coloring (AREA)
Description
〔産業上の利用分野〕
本発明は、ポリエステル系繊維の染色助剤に関
する。
〔従来の技術〕
従来、ポリエステル繊維の染色は染め足の揃つ
た分散染料と染色助剤として、高級脂肪酸エステ
ル型非イオン界面活性剤あるいはこれらとアルキ
ルエーテルサルフエートやアリールエーテルサル
フエート型などのアニオン界面活性剤の混合物を
染浴に加え、高温高圧下で均染染色する方法がと
られていた。近年、ポリエステル繊維染色の合理
化をさらに進めるために、昇温時間の短縮や経済
的染料使い(アゾ系分散染料使い)による染色コ
スト低減、あるいは高品質な染色を得るための高
堅牢度染料使い(アゾ系分散染料使い)などの要
望が強い。これらはいずれも均染染色を行うため
には余りにも過酷な染色条件であり、特に経済的
染料使いを狙つた染色処方すなわち、染め足の異
なるアゾ系染料とアンスラキノン系染料との組合
せなどは、均染に染色することは非常に困難なも
のであつた。
現在これらの問題を解決するために、昇温速度
を従来よりダウンさせたり、染色助剤の使用量を
増加するなどによつて対処しているが、完全に不
均染を解決するには至つておらず、染色不良をし
ばしば起している。
〔発明が解決しようとする問題点〕
本発明者らは染め足の異なる染料を二種以上使
用してポリエステル系繊維を染色する場合でも、
標準的な昇温速度以上で染色することができ、染
色時間を短縮することができる染色助剤を得るべ
く鋭意検討した結果、本発明に到達した。
〔問題点を解決するための手段〕
本発明は分子中にオキシエチレン基を30〜80重
量%含有する、3〜8価の多価アルコールのオキ
シアルキレンエーテルとジカルボン酸および脂肪
族モノカルボン酸との混合エステル(A)および必要
により、()多価アルコールのオキシアルキレ
ンエーテルの脂肪族モノカルボン酸エステル(B)お
よび/またはアニオン界面活性剤(C)からなること
を特徴とするポリエステル系繊維用染色助剤であ
る。
混合エステル(A)を形成するジカルボン酸として
は炭素数2〜18のジカルボン酸たとえば、脂肪族
ジカルボン酸〔コハク酸、アジピン酸、アゼライ
ン酸、セバシン酸、ドデカン二塩基酸、ヘキサデ
カン二塩基酸、エイコサン二塩基酸、7−エチル
テトラデカン二塩基酸
7−エチルオクタデカン二塩基酸
など〕;
脂肪族不飽和ジカルボン酸(フマル酸、マレイ
ン酸、不飽和長鎖二塩基酸たとえば
HOOC(CH2)6CH=CH(CH2)6COOH、
[Industrial Field of Application] The present invention relates to a dyeing aid for polyester fibers. [Prior art] Traditionally, polyester fibers have been dyed using disperse dyes with uniform dyeing legs and higher fatty acid ester type nonionic surfactants, or these and anions such as alkyl ether sulfates and aryl ether sulfates as dyeing aids. A method was used in which a mixture of surfactants was added to the dye bath and level dyeing was carried out under high temperature and pressure. In recent years, in order to further streamline polyester fiber dyeing, efforts have been made to reduce dyeing costs by shortening heating time and using economical dyes (using azo disperse dyes), or by using high fastness dyes to obtain high quality dyeing ( There is a strong demand for products using azo disperse dyes. All of these are too harsh dyeing conditions for level dyeing, and dyeing recipes aimed at economical dye use, such as combinations of azo dyes and anthraquinone dyes with different dyeing depths, are particularly difficult. However, it was extremely difficult to dye evenly. Currently, efforts are being made to solve these problems by lowering the heating rate and increasing the amount of dyeing aids used, but this has not yet completely resolved uneven dyeing. This often results in poor dyeing. [Problems to be Solved by the Invention] The present inventors have solved the problem even when dyeing polyester fibers using two or more types of dyes with different dyeing depths.
As a result of intensive studies to obtain a dyeing aid that can dye at a rate higher than the standard heating rate and shorten the dyeing time, the present invention was arrived at. [Means for solving the problems] The present invention uses an oxyalkylene ether of a trihydric to octahydric alcohol containing 30 to 80% by weight of oxyethylene groups in the molecule, a dicarboxylic acid, and an aliphatic monocarboxylic acid. (A) and, if necessary, (B) an aliphatic monocarboxylic acid ester of an oxyalkylene ether of a polyhydric alcohol and/or an anionic surfactant (C). It is a dyeing aid. Dicarboxylic acids forming the mixed ester (A) include dicarboxylic acids having 2 to 18 carbon atoms, such as aliphatic dicarboxylic acids [succinic acid, adipic acid, azelaic acid, sebacic acid, dodecane dibasic acid, hexadecane dibasic acid, eicosane Dibasic acid, 7-ethyltetradecane dibasic acid 7-Ethyl octadecane dibasic acid ]; Aliphatic unsaturated dicarboxylic acids (fumaric acid, maleic acid, unsaturated long chain dibasic acids such as HOOC(CH 2 ) 6 CH=CH(CH 2 ) 6 COOH,
以下実施例により本発明をさらに説明するが、
本発明はこれに限定されるものではない。実施例
1〜9および比較例1〜4の本発明の染色助剤お
よび比較品を第1表に示す。
The present invention will be further explained below with reference to Examples.
The present invention is not limited to this. The dyeing aids of the present invention and comparative products of Examples 1 to 9 and Comparative Examples 1 to 4 are shown in Table 1.
【表】
実施例 10
実施例1〜9の染色助剤および比較例1〜4の
化合物について、(イ)均染性試験、(ロ)分散性試験お
よび(ハ)起泡性試験を行い、その結果を第2表およ
び第3表に示した。[Table] Example 10 The dyeing aids of Examples 1 to 9 and the compounds of Comparative Examples 1 to 4 were subjected to (a) level dyeing test, (b) dispersibility test, and (c) foaming test, The results are shown in Tables 2 and 3.
【表】【table】
(イ) 均染性試験
下記の染色条件でポリエステルタフタを染色
し、染色布の左側部、右側部のL、a、b値を
測色し、色差(△E)を算出した。△Eの数値
が小さいものが均染染色であることを示す。
染料
ホロン ブリリアント ブルー SRグラン
200% 0.3%o・w・f・〔サンド化学(株)
製〕
パラニイル イエロー 3G 0.5%o.w.f.
〔B・A・S・F社製〕
染料
スミカロン イエロー SE−3GLコンク
0.25%o・w・f・
スミカロン ブリリアント レツド SE−
BL 0.5%o・w・f・
スミカロン ブルー SE−RF 0.5%o・
w・f・〔住友化学(株)製〕
染料
ホロン イエローブラウン S−2RL 0.088
%o・w・f・
ホロン ブロンルビン 2GFL 0.011%o・
w・f・
ホロン ネービー 2GLN 0.139%o・w・
f・〔サンド化学(株)製〕
染料
ダイアニツクス ブリリアント イエロー
5GE 0.2%o・w・f・
ダイアニツクス レツド BN−SE 0.25%
o・w・f・
ダイアニツクス ターコイズブルー GFS
0.65%o・w・f・〔三菱化成(株)製〕
染 浴
染料;上記
染色助剤;0.3g/(固形分)
PH;4(80%酢酸 0.3c.c./
浴比;1:20
温度、時間;60℃〓130℃(2℃/分昇温)、
130℃、30分染色、130℃〓90℃(3℃/分降
温)、湯洗、水洗、乾燥
測色;測色色差計 DICOM ND−504DE〔日
本電色(株)製〕
(ロ) 分散性試験
カラーペツトホルダーにポリエステルメリヤ
スを巻き付け下記条件で染色し、染色布の最内
部の染料の凝集付着状態(ケーシングスポツ
ト)の多少を肉眼判定した。染料凝集物のほと
んど付着していないものを5級、著しく付着し
ているものを1級と判定し、その間を5段階に
ランク付けした。
(条件)
染料
ダイアニツクス ターコイズブルー GFS
3%o・w・f・〔三菱化成(株)製〕
レゾリン ブルー FBL 3%o・w・f・
〔バイエル社製〕
染料
カヤロン ポリエステル オレンジ Bコン
ク 3%o・w・f・〔日本化薬(株)製〕
ダイアニツクス レツド BN−SE 3%
o・w・f・〔三菱化成(株)製〕
浴比;1:20
PH;5(80%酢酸 0.3c.c./)
温度、時間;60℃×5分、60℃〓90℃(1℃/
分昇温)90℃で取り出し
染色機;カラーペツト24〔辻井染機(株)製〕
(ハ) 起泡性試験
下記染浴5を試験機に入れ、溶液循環させ
る。加熱昇温して各温度到達後液流を停止し、
5秒後の起泡量を測定した。
(条件)
染 浴
染色助剤
ダイアニツクス ブラツク HG−FS 5
g/
ダイアニツクス オレンジ B−SE 5g/
〔三菱化成(株)製〕
PH;5(80%酢酸 0.3c.c./)
循環流速;2/分、ノズル径1mm
試験機;高圧噴射液流起泡試験機
〔発明の効果〕
本発明の染色助剤は、二種以上の染め足の異な
る分散染料を用いて、急昇温による苛酷な染色条
件においても染め面の良好な均染染色を可能なら
しめ、再現性良好な染色ができる。
低起泡性であるため、ラピツド液流染色機にお
いても、全く起泡によるトラブルは発生しない。
(B) Level dyeing test Polyester taffeta was dyed under the following dyeing conditions, and the L, a, and b values of the left and right sides of the dyed cloth were measured to calculate the color difference (ΔE). A small value of ΔE indicates level dyeing. Dye Holon Brilliant Blue SR Gran
200% 0.3% o.w.f. [Sandoz Chemical Co., Ltd.]
Made by Paranil Yellow 3G 0.5%owf
[Manufactured by B.A.S.F.] Dye Sumikalon Yellow SE-3GL Conch
0.25% o・w・f・ Sumikaron Brilliant Red SE−
BL 0.5%o・w・f・ Sumikaron Blue SE−RF 0.5%o・
w・f・[Sumitomo Chemical Co., Ltd.] Dye Holon Yellow Brown S-2RL 0.088
%o・w・f・ Holon Bronrubin 2GFL 0.011%o・
w・f・ Holon Navy 2GLN 0.139% o・w・
f. [Manufactured by Sandoz Kagaku Co., Ltd.] Dye Dianics Brilliant Yellow
5GE 0.2%o・w・f・dianics Red BN-SE 0.25%
o・w・f・dianics turquoise blue GFS
0.65% o・w・f・[manufactured by Mitsubishi Kasei Corporation] Dye bath Dye; above Dyeing aid; 0.3 g/(solid content) PH; 4 (80% acetic acid 0.3 cc/bath ratio; 1:20 Temperature; Time: 60℃〓130℃ (2℃/min temperature increase),
130℃, 30 minutes dyeing, 130℃〓90℃ (temperature decrease 3℃/min), hot water washing, water washing, drying Colorimetry: Colorimetric color difference meter DICOM ND-504DE [manufactured by Nippon Denshoku Co., Ltd.] (b) Dispersion Property Test A polyester knitted cloth was wrapped around a colored pet holder and dyed under the following conditions, and the degree of coagulation and adhesion of the dye (casing spot) in the innermost part of the dyed cloth was visually determined. A sample with hardly any dye aggregates attached was graded as 5th grade, a sample with a significant amount of dye aggregate was graded as 1st grade, and the in-between grades were ranked into 5 levels. (Conditions) Dye Dianics Turquoise Blue GFS
3%o・w・f・[manufactured by Mitsubishi Kasei Corporation] Resolin Blue FBL 3%o・w・f・
[Manufactured by Bayer] Dye Kayalon Polyester Orange B Conc 3% o・w・f・[Manufactured by Nippon Kayaku Co., Ltd.] Dianics Red BN-SE 3%
o・w・f・[manufactured by Mitsubishi Kasei Corporation] Bath ratio: 1:20 PH: 5 (80% acetic acid 0.3cc/) Temperature, time: 60℃ x 5 minutes, 60℃〓90℃ (1℃/
Dyeing machine: Colorpet 24 [manufactured by Tsujii Someki Co., Ltd.] (c) Foaming test Place dye bath 5 below into the test machine and circulate the solution. The temperature is increased and the liquid flow is stopped after each temperature is reached.
The amount of foaming was measured after 5 seconds. (Conditions) Dye bath Dyeing aid Dianics Black HG-FS 5
g/ Dianics Orange B-SE 5g/
[Made by Mitsubishi Kasei Corporation] PH: 5 (80% acetic acid 0.3 cc/) Circulating flow rate: 2/min, nozzle diameter 1 mm Testing machine: High-pressure injection liquid flow foaming tester [Effects of the invention] Dyeing assistant of the present invention The agent uses two or more types of disperse dyes with different dyeing feet to enable level dyeing with good dyed surfaces even under severe dyeing conditions due to rapid temperature rise, and dyeing with good reproducibility. Since it has low foaming properties, no troubles due to foaming occur even in rapid jet dyeing machines.
Claims (1)
量%含有する、3〜8価の多価アルコールのオキ
シアルキレンエーテルとジカルボン酸および脂肪
族モノカルボン酸との混合エステル(A)、および必
要により()多価アルコールのオキシアルキレ
ンエーテルの脂肪族モノカルボン酸エステル(B)お
よび/またはアニオン界面活性剤(C)からなること
を特徴とするポリエステル系繊維用染色助剤。 2 (A)が一般式 {式中Xはジカルボン残基;Aはアルキレン基;
Yは3〜8価の多価アルコール残基;ZはHまた
はRCOで、Rは脂肪族モノカルボン酸残基であ
る。(ただし、Zの少なくとも1個はRCOであ
る)oは3〜8の整数、nは0〜50の整数、nの合計は
4〜200の整数である。)で示される化合物である
特許請求の範囲の第1項記載の助剤。[Claims] 1 () A mixed ester of an oxyalkylene ether of a trihydric to octahydric alcohol, a dicarboxylic acid, and an aliphatic monocarboxylic acid, containing 30 to 80% by weight of oxyethylene groups in the molecule ( A dyeing aid for polyester fibers, characterized in that it consists of A), and optionally () an aliphatic monocarboxylic acid ester of an oxyalkylene ether of a polyhydric alcohol (B) and/or an anionic surfactant (C). 2 (A) is a general formula {In the formula, X is a dicarboxylic residue; A is an alkylene group;
Y is a trivalent to octavalent polyhydric alcohol residue; Z is H or RCO, and R is an aliphatic monocarboxylic acid residue. (However, at least one of Z is RCO.) o is an integer of 3 to 8, n is an integer of 0 to 50, and the total of n is an integer of 4 to 200. ) The auxiliary agent according to claim 1, which is a compound represented by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59230922A JPS61108781A (en) | 1984-10-31 | 1984-10-31 | Dyeing aid for polyester fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59230922A JPS61108781A (en) | 1984-10-31 | 1984-10-31 | Dyeing aid for polyester fiber |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61108781A JPS61108781A (en) | 1986-05-27 |
JPH0418070B2 true JPH0418070B2 (en) | 1992-03-26 |
Family
ID=16915383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59230922A Granted JPS61108781A (en) | 1984-10-31 | 1984-10-31 | Dyeing aid for polyester fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61108781A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5186658B2 (en) * | 2001-06-20 | 2013-04-17 | 松本油脂製薬株式会社 | Polyester fiber oligomer inhibitor |
DE10130357A1 (en) * | 2001-06-23 | 2003-01-02 | Clariant Gmbh | Pesticide preparations containing copolymers |
JP2007254904A (en) * | 2006-03-22 | 2007-10-04 | Komatsu Seiren Co Ltd | Polyester-based textile product for recycling, method for decoloring polyester-based textile product for recycling, and method for recycling polyester-based textile product |
JP4614912B2 (en) * | 2006-05-16 | 2011-01-19 | 日華化学株式会社 | Oligomer remover for polyester fiber materials |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51122020A (en) * | 1975-04-04 | 1976-10-25 | Ciba Geigy Ag | Propylene oxide reaction products * their preparation or dying or printing method by utilizing said products |
-
1984
- 1984-10-31 JP JP59230922A patent/JPS61108781A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51122020A (en) * | 1975-04-04 | 1976-10-25 | Ciba Geigy Ag | Propylene oxide reaction products * their preparation or dying or printing method by utilizing said products |
Also Published As
Publication number | Publication date |
---|---|
JPS61108781A (en) | 1986-05-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH11158402A (en) | Disperse dye composition and method for coloring hydrophobic material therewith | |
KR100395145B1 (en) | Dyeing of disperse dye compositions and hydrophobic materials using them | |
US4396393A (en) | Dye mixtures and their use | |
JPH0418070B2 (en) | ||
US4343620A (en) | Propylene oxide polyadducts containing carboxyl groups and their salts | |
EP0491386B1 (en) | Disperse dye mixture and dyeing method employing it | |
JPH10237335A (en) | Disperse dye composition | |
EP0235088B1 (en) | Halfesters of maleic acid or phthalic acid and alkoxylated fatty amines | |
US4362530A (en) | Dyeing auxiliaries containing mixed anionic, cationic and non-ionic ethylene oxide adducts | |
US3681005A (en) | Dyeing wool in fibrous material containing wool with 1:2 metal complex azo dyes,acid and aromatic hydro-carbons,carboxylic acids/esters or phenols | |
US4432770A (en) | Rapid dyeing of polyester fibers with a mixture of disperse dyes | |
US4097233A (en) | Basic dye composition | |
DE3347572A1 (en) | MIXTURES OF BLUE DISPERSION AZO DYES FOR DYEING POLYESTER FIBERS | |
EP0373247A1 (en) | Dye-leveling agent and dyeing method | |
GB2147319A (en) | Level dyeing of wool fibres | |
CN104884539B (en) | It is a kind of blue to black disperse dye compound and its application | |
JPS5911364A (en) | Dyeing of hydrophobic fiber | |
US4191532A (en) | Organic compounds | |
JP3746341B2 (en) | Disperse dye composition and method for dyeing hydrophobic fibers using the same | |
JP2913254B2 (en) | Water-insoluble disperse dye composition and method for dyeing polyester fiber using the same | |
KR20080052651A (en) | Dyeing of wool fibres | |
JPH08100132A (en) | Orange disperse dye composition and dyeing hydrophobic fiber material using the same | |
CN114231051B (en) | High-fastness disperse dye composition, disperse dye, and preparation method and application thereof | |
JPH10140029A (en) | Disperse dye composition and dyeing of hydrophobic fibers by using the same | |
KR20040062427A (en) | Use of pigments as disperse dyestuffs |