EP2721113A1 - Säurefarbstoffmischungen für polyamid und wolle enthaltend dimere säurefarbstoffe - Google Patents
Säurefarbstoffmischungen für polyamid und wolle enthaltend dimere säurefarbstoffeInfo
- Publication number
- EP2721113A1 EP2721113A1 EP12727801.8A EP12727801A EP2721113A1 EP 2721113 A1 EP2721113 A1 EP 2721113A1 EP 12727801 A EP12727801 A EP 12727801A EP 2721113 A1 EP2721113 A1 EP 2721113A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dye
- hydrogen
- acid
- sulfo
- wool
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/24—Polyamides; Polyurethanes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/24—Polyamides; Polyurethanes
- D06P3/241—Polyamides; Polyurethanes using acid dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
Definitions
- Acid dyes are mainly used to dye wool, others
- Acid dye on polyamide can differ significantly from those on wool. These are, for example, the color itself
- Acid dye mixture on polyamide, wool and on polyamide / wool blended fibers provides good reproducible colorations with good wet fastness.
- the present invention is an acid dye mixture comprising
- R1 is H, d-Ce-alkyl
- R 2 is H, C 1 -C 6 alkyl; b) from 5 to 30% by weight, preferably from 5 to 20% by weight, particularly preferably from 10 to 15% by weight, of at least one dye B having the general structure (B)
- R 3 is H, phenyl, where phenyl is substituted or unsubstituted
- C C double bond an unsubstituted or substituted phenyl ring, R6 H, sulfo;
- weight percentages are based on the total weight of the
- Acid dye mixture are related.
- the positive charge in formula (B) is usually substituted by a negative charge of a sulfo group contained in the molecule or by an equivalent of an anion, e.g. B. Cl " , VT S0 4 2" neutralized.
- sulfo is a radical of formula S0 3 M.
- M is preferably a single negative charge, hydrogen, an alkali metal or ammonium.
- alkali metal preferably means Li, Na, or K, especially Na.
- ammonium is preferably NH 4 + ,
- Substituted phenyl ring preferably denotes a phenyl radical which is mono- or polysubstituted, preferably mono-, di- or trisubstituted, by one or more substituents selected from the group consisting of C 1 -C 4 -alkyl, halogen, C 1 -C 4 -alkoxy, hydroxy, sulfo , Amino or nitro are particularly preferred substituents are methyl, Cl, amino, methoxy, ethoxy and sulfo.
- R 1 and R 2 independently of one another are hydrogen or methyl.
- R 3 is hydrogen, unsubstituted phenyl or phenyl substituted with amino, sulfo and / or ethoxy.
- R5 is hydrogen or methoxy, or in a likewise preferred embodiment, R4 and R5
- Preferred dyes of the formula (B) are those in which
- R3 is hydrogen or unsubstituted phenyl
- R4 is hydrogen or sulfo
- R5 is hydrogen or methoxy
- R6 is hydrogen or sulfo
- R3 is phenyl substituted with amino, sulfo and / or ethoxy
- R4 is hydrogen or sulfo
- R6 is hydrogen
- the dyes of the formulas (A) and (B) are known per se and can be prepared by known methods, for example as described in: Ulimann, 6.Aveml., 0.1002 / 14356007. a02_355, pages 1 - 68
- Another object of the present invention is a process for the preparation of the acid dye mixture described above, by mixing the at least one dye A with the at least one dye B in the weight ratios indicated above, for example in the form of their dry powder, press cake or preferably aqueous solutions.
- the dyes A and B can also be mixed together only in the dyebath.
- the dye mixtures according to the invention are particularly suitable for fibrous material which consists of natural and / or synthetic
- Polyamides consists of dyeing or printing in blue tones.
- the dye mixtures according to the invention are also suitable for producing inkjet printing inks and for printing with these fibrous material which consists of natural and / or synthetic polyamides or cellulose (eg paper).
- Another object of the invention is the use of said
- Another object of the invention is the use of said
- the dyeing is carried out according to known methods, such as. B. the
- the substrate to be dyed z. B. in the form of yarn, fabric, knitted or carpet. Fully-fashioned dyeings are also on delicate substrates, eg. Lambswool, cashmere, alpaca and mohair very well possible. Particularly suitable are the dye mixtures according to the invention for dyeing fine-denier fibers (microfibers).
- the dye mixtures according to the invention show good compatibility with known acid dyes. Accordingly, the dye mixtures may be used alone in a dyeing or printing process or as a blue component in a combination dyeing or printing composition along with other acid dyes of the same class, i. H. With
- Acid dyes which have comparable dyeing properties, such as fastness properties and Ausziehraten from Därbebad on the substrate.
- the dyes of the present invention may be used in conjunction with other acid dyes.
- the dye mixtures according to the invention are particularly suitable for dyeing wool, silk and all nylon types on which dyeings having a high level of fastness, in particular good light fastness and good
- the dye mixtures according to the invention can also be used as blue components in the trichromatic dyeing process or trichromatic printing process.
- Trichromiefärben or printing can be used on all conventional and known dyeing and printing methods, such as. B. the
- Trichromatic dye mixture used in the process of the invention depends on the desired shade. For a shade of brown you can
- a yellow component 20-40% by weight of a yellow component, 40-60% by weight of an orange or red component and 10-20% by weight of an acid dye mixture according to the invention are used as the blue component.
- parts are parts by weight and percentages are by weight.
- a dyebath of 40 ° C consisting of 2000 parts of water, 1 part of a weakly cationic, dye-affinity leveling agent based on an ethoxylated aminopropyl fatty acid amide, 0.25 parts of the following
- Example 1b (wool dyeing):
- a dyebath of 40 ° C consisting of 4000 parts of water, 1 part of a weakly dye affinity leveling agent with amphoteric character on the basis of a sulfated, ethoxylated fatty acid amide, 0.4 parts of the dye mixture of Example 1a, with 1 - 2 parts 40% Acetic acid was adjusted to pH 5, 100 parts of wool fabric are added. After 10 minutes at 40 ° C, the dyebath with a temperature increase of 1 ° C per minute on
- Wool fabric is taken out of the bath, rinsed with warm and then cold water and dried. The result is a blue level wool dyeing with good light and wet fastness with excellent levelness within the fiber (root-tip).
- the dyes of Examples 2 to 18 listed in the table below are mixed in the ratio Dye B: Dye A of 1: 9 or of 2: 8 and used for dyeing in analogy to Examples 1a and 1b.
- the dye mixtures of the invention provide on the respective substrate (polyamide or wool) well reproducible, level dyeings with very good wet and light fastness. 10
- a dye bath of 40 ° C consisting of 2000 parts of water, 1 part of a weakly cationic dye-like leveling agent based on an ethoxylated Aminopropylfettklamids, 0.3 parts of a dye mixture from Example 1a, with 1-2 parts of 40% acetic acid to pH 5.5, 100 parts of nylon 6,6 fabric are added. After 10 minutes at 40 ° C, the dyebath is heated with a temperature increase of 1.5 ° C per minute to 120 ° C and then left for 15-25 minutes at this temperature.
- Polyamide 6,6 fabric is removed from the dyebath, rinsed with warm and then cold water and dried. It results in a blue one
- Dye mixture from Example 1a which was adjusted to pH 5 with 1 to 2 parts of 40% acetic acid are added to 100 parts of polyamide 6.6 fabric. After 10 minutes at 40 ° C, the dyebath is heated with a temperature increase of 1 ° C per minute to 98 ° C and then left for 45 to 60 minutes at boiling temperature. It is then cooled to 70 ° C within 15 minutes. The dyed fabric is removed from the bath, rinsed with warm and then cold water and dried. The result is a level gray polyamide dyeing, which shows good light and wet fastness.
- Example 23 Example 23
- Example 24 (wool / polyamide blended fabric dyeing)
- a dyebath of 40 ° C consisting of 4000 parts of water, 1 part of a weakly dye affinity leveling agent with amphoteric character on the basis of a sulfated, ethoxylated fatty acid amide, 0.4 parts of the dye mixture of Example 1a, with 1 - 2 parts 40% Acetic acid adjusted to pH 5 100 parts of wool / polyamide blended fabric are added.
- the dyebath is heated to boiling temperature with a temperature increase of 1 ° C per minute and then left for 40 - 60 minutes at boiling temperature.
- the mixture is then cooled to 70 ° C within 20 minutes.
- the dyed wool / polyamide blend is removed from the bath, rinsed with warm and then cold water and dried. The result is a blue level wool / polyamide blend fabric dyeing with good light and wet fastness properties with excellent levelness within the wool fiber (root-lace) and equal shade on nylon and wool fibers.
- Example 1a prepared and a polyamide 6 fabric dyed analogously to Example 1a.
- Example 1b prepared and a wool fabric dyed analogously to Example 1b. It creates a restless appearance.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102011104362 | 2011-06-16 | ||
PCT/EP2012/002497 WO2012171638A1 (de) | 2011-06-16 | 2012-06-13 | Säurefarbstoffmischungen für polyamid und wolle enthaltend dimere säurefarbstoffe |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2721113A1 true EP2721113A1 (de) | 2014-04-23 |
Family
ID=46317338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP12727801.8A Withdrawn EP2721113A1 (de) | 2011-06-16 | 2012-06-13 | Säurefarbstoffmischungen für polyamid und wolle enthaltend dimere säurefarbstoffe |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP2721113A1 (zh) |
JP (1) | JP2014519543A (zh) |
KR (1) | KR20140041744A (zh) |
CN (1) | CN103619962A (zh) |
BR (1) | BR112013032249A2 (zh) |
MX (1) | MX2013014769A (zh) |
TW (1) | TW201313840A (zh) |
WO (1) | WO2012171638A1 (zh) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB201611573D0 (en) | 2016-07-01 | 2016-08-17 | Technip France Sas | Cracking furnace |
CN110128847B (zh) * | 2019-05-18 | 2020-09-29 | 上海雅运新材料有限公司 | 一种蓝色酸性染料组合物及其在纤维上的染色应用 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH624132A5 (zh) * | 1976-07-22 | 1981-07-15 | Ciba Geigy Ag | |
US4514187A (en) * | 1982-07-21 | 1985-04-30 | Ciba-Geigy Corporation | Process for dyeing differential-dyeing polyamide fibres |
EP0127579B1 (de) * | 1983-05-25 | 1987-10-07 | Ciba-Geigy Ag | Verfahren zum Trichromie-Färben oder -Bedrucken |
GB8424137D0 (en) * | 1983-09-29 | 1984-10-31 | Sandoz Ltd | Organic compounds |
JP3290486B2 (ja) * | 1992-12-14 | 2002-06-10 | 田岡化学工業株式会社 | ポリアミド繊維用染料組成物、その染色法及びその染色物 |
DE59607383D1 (de) * | 1995-02-10 | 2001-09-06 | Ciba Sc Holding Ag | Farbstoffmischungen und ihre Verwendung |
JP4073202B2 (ja) * | 2000-11-13 | 2008-04-09 | オリヱント化学工業株式会社 | レーザー光透過性着色樹脂組成物用着色剤及びその関連技術 |
ATE302822T1 (de) | 2000-12-05 | 2005-09-15 | Clariant Finance Bvi Ltd | Trichromie-faerbeverfahren |
WO2008017570A1 (en) * | 2006-08-10 | 2008-02-14 | Unilever Plc | Shading composition |
WO2008090091A1 (en) * | 2007-01-26 | 2008-07-31 | Unilever Plc | Shading composition |
ES2532473T3 (es) * | 2009-10-13 | 2015-03-27 | Unilever N.V. | Polímeros colorantes |
-
2012
- 2012-06-05 TW TW101120114A patent/TW201313840A/zh unknown
- 2012-06-13 MX MX2013014769A patent/MX2013014769A/es unknown
- 2012-06-13 JP JP2014515091A patent/JP2014519543A/ja active Pending
- 2012-06-13 WO PCT/EP2012/002497 patent/WO2012171638A1/de active Application Filing
- 2012-06-13 KR KR1020147001074A patent/KR20140041744A/ko not_active Application Discontinuation
- 2012-06-13 BR BR112013032249A patent/BR112013032249A2/pt not_active IP Right Cessation
- 2012-06-13 EP EP12727801.8A patent/EP2721113A1/de not_active Withdrawn
- 2012-06-13 CN CN201280029412.7A patent/CN103619962A/zh active Pending
Non-Patent Citations (1)
Title |
---|
See references of WO2012171638A1 * |
Also Published As
Publication number | Publication date |
---|---|
TW201313840A (zh) | 2013-04-01 |
MX2013014769A (es) | 2014-07-30 |
JP2014519543A (ja) | 2014-08-14 |
WO2012171638A1 (de) | 2012-12-20 |
CN103619962A (zh) | 2014-03-05 |
BR112013032249A2 (pt) | 2016-12-20 |
KR20140041744A (ko) | 2014-04-04 |
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RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: ARCHROMA IP GMBH |
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RIC1 | Information provided on ipc code assigned before grant |
Ipc: C09B 67/22 20060101ALI20160309BHEP Ipc: D06P 5/00 20060101AFI20160309BHEP Ipc: D06P 3/24 20060101ALI20160309BHEP |
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Effective date: 20160907 |