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EP0455055B1 - Teinture avec des colorants réactifs en bains fixes suivant le procédé par épuisement - Google Patents

Teinture avec des colorants réactifs en bains fixes suivant le procédé par épuisement Download PDF

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Publication number
EP0455055B1
EP0455055B1 EP91106186A EP91106186A EP0455055B1 EP 0455055 B1 EP0455055 B1 EP 0455055B1 EP 91106186 A EP91106186 A EP 91106186A EP 91106186 A EP91106186 A EP 91106186A EP 0455055 B1 EP0455055 B1 EP 0455055B1
Authority
EP
European Patent Office
Prior art keywords
dyeing
parts
liquor
dye
salt
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
Application number
EP91106186A
Other languages
German (de)
English (en)
Other versions
EP0455055A2 (fr
EP0455055A3 (en
Inventor
Dietrich Dr. Hildebrand
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.)
Bayer AG
Original Assignee
Bayer AG
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Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Publication of EP0455055A2 publication Critical patent/EP0455055A2/fr
Publication of EP0455055A3 publication Critical patent/EP0455055A3/de
Application granted granted Critical
Publication of EP0455055B1 publication Critical patent/EP0455055B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/66Natural or regenerated cellulose using reactive dyes
    • D06P3/666Natural or regenerated cellulose using reactive dyes reactive group not directly attached to heterocyclic group
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/0004General aspects of dyeing
    • D06P1/002Processing by repeated dyeing, e.g. in different baths
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/38General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes
    • D06P1/382General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes reactive group directly attached to heterocyclic group
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/38General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes
    • D06P1/384General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes reactive group not directly attached to heterocyclic group
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/66Natural or regenerated cellulose using reactive dyes
    • D06P3/663Natural or regenerated cellulose using reactive dyes reactive group directly attached to heterocyclic group
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/916Natural fiber dyeing
    • Y10S8/918Cellulose textile

Definitions

  • the present invention relates to a process for the salt-saving dyeing of cellulose fiber material with reactive dyes from electrolyte-containing baths at 40 ° C to 130 ° C by the exhaust method.
  • cellulose fiber materials such as cotton, cellulose materials and linen are usually dyed from dyebaths containing 5 to 120 g / l of sodium chloride or sodium sulfate, which, depending on the dyeing temperature, have a pH of 6 to 12 at 40 to 130 ° C.
  • the salt necessary for drawing up the dye onto the fiber material is added at the beginning of the dyeing process before the dye and in the other method after the dye has been added.
  • the addition of the salt before adding the dye is preferred for technical reasons because of the easier handling.
  • the start of the dyeing process with the liquor containing the salt is therefore a technically established procedure.
  • the introduction of the salt into the dyeing liquor can be done by using salt, i.e. Let in a highly concentrated salt solution or by adding salt in solid form to the circulating liquor.
  • the liquor containing the salt is drained off and the dyed textile material is cleaned of non-fixed residual dye by rinsing and washing.
  • the salt content of the drained remaining liquor is 5 to 120 g / l depending on the color depth of the dyeing carried out.
  • the total salt consumption of the coloring is 2.5 to 250 kg per 100 kg of dyed material, depending on the color depth.
  • the salt content of the residual reactive dyeing liquors is therefore not only an ecological burden on the wastewater, but also represents a significant proportion of the total chemical costs to be used for the preparation of the reactive dyeing.
  • a process has now been found for dyeing cellulose materials from salt-containing baths with reactive dyes using the exhaust method, which is characterized in that the exhausted bath used for the previous dyeing is adjusted after the volume, salinity, initial pH value and dye concentration can be reused without further cleaning operation.
  • the reuse of a dye liquor that has already been used thus permits at least partial reuse of the amount of salt used for the previous dyeing.
  • the portion of the remaining liquor that remains in the material to be separated after dyeing when the material to be dyed and the remaining liquor are separated is removed by a repeated rinsing process.
  • the amount of salt contained in the remaining liquor portion bound by the material to be dyed is thus transferred to the rinsing liquor and, because of its low concentration, is only of interest in special cases.
  • the rinsing liquors can also be partially collected and used again for subsequent staining.
  • the amounts of salt bound in the material to be dyed and removed by the rinsing process are replaced by adding fresh salt of the same type.
  • the amount of residual liquor bound by the material to be dyed is 200-300%, based on the amount of textile material used. Accordingly, by re-use of residual reactive dye liquors saves 1 to 200 kg salt (table salt or sodium sulfate) per 100 kg of the textile material to be dyed, depending on the color depth, liquor length and retention capacity of the goods.
  • the dyeing time required to achieve the desired depth of color is extended by about 15-60 minutes and / or the dyeing temperature is increased after reaching the desired depth of color, for example by 10 ° C. to 20 ° C.
  • the dyeing is carried out in a known manner, for example by automated control of the addition of alkali or the pH (cf. Le A 25 166). It is expedient to use dyeing units which have a conductivity measuring cell for automatic control and adjustment of a defined electrolyte content.
  • the dyeing units expediently contain an additional vessel for holding the dyeing liquor mentioned.
  • Alkali metal hydroxides (LiOH, NaOH, KOH) are preferably used as the fixing alkali. Soda can also be used, for example.
  • the process according to the invention can be used to dye one after the other using the same or different dyes.
  • water-soluble reactive dyes are suitable as reactive dyes, for example those of the azo, anthraquinone, phthalocyanine, formazane or triphendioxazine series.
  • the process is preferably suitable for dyes with a reactive substituent on a 5- or 6-membered aromatic-heterocyclic ring, for example a sym.
  • a reactive substituent on a 5- or 6-membered aromatic-heterocyclic ring for example a sym.
  • Triazinyl, pyrimidinyl or quinoxalinyl ring Possible reactive substituents are, for example, Cl, Br, F, ammonium, hydrazinium, pyridinium (with substituents such as COOH, CH3).
  • the process is particularly suitable for dyes with a monochlorotriazinyl, monofluorotriazinyl, mono-nicotinyltriazinyl, 2,6-difluoro-5-chloro-pyrimidinyl or 5-chloro-6-fluoropyrimidinyl radical.
  • 100 parts of a bleached cotton material are treated for one hour in a dyeing machine with 2000 parts of a 50 ° C. aqueous liquor which contains 2 parts of dye I, 1 part of sodium bicarbonate, 12.6 parts of caustic soda and 100 parts of sodium chloride in solution.
  • the exhausted dye bath is allowed to drain into a storage container.
  • the retention capacity of the goods is 300 parts of the fleet used.
  • the expired fleet consists of 1,700 parts of the original fleet.
  • the dyeing unit is then filled twice with fresh water at 60 ° C. and drained off after a treatment of 5 minutes. The drained fleet is led into the sewage system.
  • the dyeing is then treated twice with water at 80 ° C. for 10 minutes each.
  • the stained fleets are drained. Then it is filled with 1700 parts of fresh water, brought to the boiling temperature and treated for 10 minutes.
  • the liquor is drained, rinsed cold with fresh water and the dyeing is removed from the dyeing unit.
  • the dyeing unit is then loaded with 100 parts of a bleached, undyed cotton material.
  • the 60 parts of sodium chloride in solid form are added to the remaining liquor of the first color transferred to the storage container and brought into solution by means of an agitator.
  • the alkaline liquor is then adjusted to pH 6 using a dilute hydrochloric acid dissolved in 25 parts of water, the acid required being determined in a preliminary test.
  • the neutral, saline liquor is then pumped back into the dyeing unit and heated to 50 ° C. After this temperature has been reached, a 50 ° C. warm solution of 4 parts of dye II in 150 parts of water is prepared while metering in linearly over 45 minutes.
  • the dyeing is then treated twice with water at 80 ° C. for 10 minutes each.
  • the stained fleets are drained.
  • the liquor is drained, rinsed cold with fresh water and the dye is removed from the dyeing unit.
  • a blue dyeing is obtained in the first dyeing process and a red dyeing with good fastness properties in each case in the second dyeing process.
  • 100 parts of a bleached cotton material are treated for one hour in a dyeing machine with 1000 parts of an 80 ° C. aqueous liquor of pH 9.4 which contains 2 parts of dye III, 2 parts of sodium bicarbonate, 4 parts of soda and 80 parts of sodium chloride. Thereafter, treatment is carried out at 95 ° C. for 10 minutes and the liquor is pumped off and transferred to a batch vessel which has a volume which corresponds to 100% of the dyeing volume of the dyeing unit.
  • the pumped out fleet consists of 700 parts of the original dyeing fleet.
  • the dyeing unit is then filled twice with fresh water at 60 ° C and drained after 5 minutes; the drained fleet is fed into the sewage system.
  • the dyeing is then treated twice with water at 80 ° C. for 10 minutes each.
  • the stained fleets are drained.
  • the dyeing unit is then equipped with 100 parts of a corresponding undyed cotton material.
  • the residual liquor of the first dyeing transferred into the batch vessel is adjusted to pH 6 with 100 parts of an aqueous solution containing dilute hydrochloric acid and 100 parts of an aqueous solution are added which contain 20 parts of sodium chloride, then 2 parts of dye III are dissolved in 100 parts Water was added and the dye liquor obtained was transferred to the dyeing unit.
  • the liquor is heated to 80 ° C. and allowed to circulate with the goods for 30 minutes.
  • an aqueous solution which contain 2 parts of sodium bicarbonate and 4 parts of soda, are metered in uniformly over a 30-minute period with vigorous liquor circulation according to a linear dosing curve.
  • the dyeing is then carried out for 1 hour at this temperature and then the remaining liquor is pumped off, as in the first dyeing, and the dyeing is rinsed and aftertreated.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Claims (3)

  1. Procédé de teinture par étapes successives de matières à base de fibres cellulosiques à l'aide de colorants réactifs d'après la technique de l'épuisement en bain unique, caractérisé en ce qu'on réutilise le bain épuisé ayant servi à la teinture précédente, après ajustement du volume, de la teneur en sel, de la valeur initiale de pH et de la concentration en colorant nécessaires pour chaque teinture suivante sans autre opération de purification.
  2. Procédé suivant la revendication 1, caractérisé en ce que lorsque la profondeur de teinte désirée a été atteinte, on maintient la température de teinture pendant 15 à 60 minutes à la valeur correspondante ou à 10-20°C au-dessus de la valeur correspondante.
  3. Procédé suivant les revendications 1-2, caractérisé en ce qu'on utilise, pour compléter le bain de teinture de l'opération de teinture précédente, les bains de rinçage venant de l'opération de teinture précédente.
EP91106186A 1990-05-01 1991-04-18 Teinture avec des colorants réactifs en bains fixes suivant le procédé par épuisement Expired - Lifetime EP0455055B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4013987A DE4013987A1 (de) 1990-05-01 1990-05-01 Faerben mit reaktivfarbstoffen aus stehenden baedern nach dem ausziehverfahren
DE4013987 1990-05-01

Publications (3)

Publication Number Publication Date
EP0455055A2 EP0455055A2 (fr) 1991-11-06
EP0455055A3 EP0455055A3 (en) 1992-02-26
EP0455055B1 true EP0455055B1 (fr) 1994-03-16

Family

ID=6405514

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91106186A Expired - Lifetime EP0455055B1 (fr) 1990-05-01 1991-04-18 Teinture avec des colorants réactifs en bains fixes suivant le procédé par épuisement

Country Status (4)

Country Link
US (1) US5139533A (fr)
EP (1) EP0455055B1 (fr)
JP (1) JPH04228686A (fr)
DE (2) DE4013987A1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5330539A (en) * 1991-12-18 1994-07-19 Hoechst Celanese Corporation Fiber reactive dyes - applications with low salt
DE59409489D1 (de) * 1993-05-18 2000-09-28 Dystar Textilfarben Gmbh & Co Triphendioxazinverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Farbstoffe
US6056790A (en) * 1998-05-27 2000-05-02 Georgia Tech Research Corp. Method for automated dyebath reuse
US6753956B2 (en) 1998-05-27 2004-06-22 Georgia Tech Research Corp. Automated analysis system for a dyebath
JP2001146690A (ja) * 1999-11-24 2001-05-29 Hakuto Co Ltd 染色残液の再使用方法および染料除去剤の再生方法
US20090223001A1 (en) * 2008-03-05 2009-09-10 Kenneth Kuk-Kei Wang Dyed, bleach-resistant fabrics and garments
BRPI0804658B1 (pt) * 2008-08-11 2012-06-26 processo de tingimento têxtil de fibras celulósicas e suas combinações com outras fibras com banhos de tingimentos reutilizados, sem realizar nenhum tratamento de depuração posterior.
CN103233332B (zh) * 2013-04-12 2014-02-19 机械科学研究总院先进制造技术研究中心 一种筒子纱染色过程的曲线逼近控制方法
CN104018309A (zh) * 2014-05-26 2014-09-03 浙江俏尔婷婷服饰有限公司 一种活性染料染色后残液回用的方法
CN104195848B (zh) * 2014-08-25 2016-01-20 际华三五四三针织服饰有限公司 同色-深色活性染料染针织物续缸染色方法
CN109778561B (zh) * 2019-01-24 2021-07-06 西安工程大学 基于异位矿化技术纤维素纤维活性染料染色盐回用方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1619590C3 (de) * 1965-11-05 1973-10-31 Imperial Chemical Industries Ltd., London Verfahren zum Farben von Cellu losetextilmaterialien
US4152113A (en) * 1978-01-26 1979-05-01 Hanes Corporation System for dyeing hosiery goods
US4292039A (en) * 1980-03-24 1981-09-29 Farris Clyde A Method and apparatus for controlling dissolved solid concentrations
EP0204656A1 (fr) * 1985-05-14 1986-12-10 Ciba-Geigy Ag Procédé de teinture de matiére textile hydrophobe

Also Published As

Publication number Publication date
EP0455055A2 (fr) 1991-11-06
DE4013987A1 (de) 1991-11-07
JPH04228686A (ja) 1992-08-18
US5139533A (en) 1992-08-18
DE59101179D1 (de) 1994-04-21
EP0455055A3 (en) 1992-02-26

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