WO1980001577A1 - Resist printing process and means for its application - Google Patents
Resist printing process and means for its application Download PDFInfo
- Publication number
- WO1980001577A1 WO1980001577A1 PCT/CH1980/000009 CH8000009W WO8001577A1 WO 1980001577 A1 WO1980001577 A1 WO 1980001577A1 CH 8000009 W CH8000009 W CH 8000009W WO 8001577 A1 WO8001577 A1 WO 8001577A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- dyes
- anionic
- colorants
- value
- dye
- Prior art date
Links
Classifications
-
- 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
- D06P1/00—General 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
- D06P1/44—General 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 insoluble pigments or auxiliary substances, e.g. binders
- D06P1/60—General 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 insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
- D06P1/607—Nitrogen-containing polyethers or their quaternary derivatives
- D06P1/6076—Nitrogen-containing polyethers or their quaternary derivatives addition products of amines and alkylene oxides or oxiranes
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/26—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds
- C22B3/38—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds containing phosphorus
- C22B3/384—Pentavalent phosphorus oxyacids, esters thereof
- C22B3/3846—Phosphoric acid, e.g. (O)P(OH)3
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/26—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds
- C22B3/38—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds containing phosphorus
- C22B3/386—Polyphosphoric oxyacids, or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/26—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds
- C22B3/38—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds containing phosphorus
- C22B3/387—Cyclic or polycyclic compounds
-
- 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
- D06P5/12—Reserving parts of the material before dyeing or printing ; Locally decreasing dye affinity by chemical means
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S534/00—Organic compounds -- part of the class 532-570 series
- Y10S534/01—Mixtures of azo compounds
Definitions
- the present invention relates to a process for dyeing with anionic dyes to produce reservation or ilulticolor effects.
- the reservation agent can first be fixed and then colored further.
- dyeing can be carried out in the presence or absence of reservation agents. If these contain reactive groups, larger amounts of them are necessary after the wet-on-wet process; if only fiber-affine agents are used, a satisfactory reserve (or multicolor effect) is generally not possible.
- the selection of suitable dyes is limited in the latter process. If a dye is displaced in the absence of reservation agents at all (e.g. mechanically), satisfactory results can generally not be achieved either.
- the present invention therefore relates to a process for the production of reserves or colored effects on textile fabrics and yarns of natural or synthetic polyamides, in which the textile material to be dyed is first sulfonated with a conventional dyeing liquor containing anionic dyes with a K ′ value ⁇ 5 1: 1 and / or 1: 2 metal complex dyestuffs, pretreated, characterized in that one or more liquors, optionally containing anionic or disperse dyestuffs or corresponding brighteners, in which, in the presence of anionic dyestuffs, these are at least one unit lower, are then present Should have a K value than that used for the dyes for the fund coloring or brighteners, which contain one or more alkoxylated fatty acids or polyamines, are applied to the substrate and then subjected to a heat treatment to fix the dyes or brighteners.
- the K-value (or K'-value) is a quantity familiar to the dyeing chemist, for its determination be it on GB-PS 14 89 456, on Bayer-Farbenrevue 21, 32 (1972) or on ifelliand 6, 641 (1973 ) referred. This value is a measure of the coloring behavior of anionic dyes in connection with their possible combinations.
- Nylon yarn (type 846 Du Pont) is treated at 40 ° C. with a standard dye of known K value and the dye to be determined.
- the amounts of dye are chosen so that a standard intensity of 1/3 SI is achieved (in the bath there are 2 g / 1 NaH 2 PO 4 and 0.3 g / l Na 2 HPO 4 , pH: 6; the liquor / product ratio is 40: 1).
- the bath is heated to 100 ° C (1 ° C / min) and the color concentration is measured spectrometrically every 5 minutes (with fast absorption every 2.5 min).
- the calculations are carried out using computers [JSDC 74, 242, (1958)].
- the test is carried out in the presence of 2% of a cathionic leveling agent (commercial product: ethoxylated aminopropyl fatty amine). This value is called the K 'value.
- a cathionic leveling agent commercial product: ethoxylated aminopropyl fatty amine
- the first stage of the process according to the invention relates to the base coloring with an anionic dye with a K ′ value ⁇ 5, preferably ⁇ 6.
- This coloring is carried out in a known manner by padding, watering, plating and other methods at room temperature.
- Preferred anionic dyes are those with two or more sulfo groups or metal complex dyes with at least one sulfo group.
- Metal complex dyes are preferably 1: 2 or 1: 1 chromium or cobalt complexes, preferably the azo or azomethine series. These are from the color-in known dex.
- auxiliaries such as thickeners, dispersants and the like, can also be used in the liquors.
- the liquor is brought to a pH of 4-7, preferably 5-6.
- the pick-up is around 60-200%, preferably 80-120% (based on the weight of the goods, dry).
- a drop of solutions a) and b) are placed on a thin chromatography layer and dried (room temperature).
- the spot of solution a) is colored on the entire (diffuse) layer, that of solution b) may only be colored in the middle and must be almost colorless at the edge.
- alkoxylated fatty (poly) amines according to the invention are dispersants with leveling or retarding properties, preferably of the cathionically active or amphoteric type, but preferably of the cationic type. They contain no fiber-reactive groups and are preferably those of the formula I below
- m is 0 to 6, n 2 or 3, x, y u. z is 1 to 100 and together 10 to 100 is a C 10 -C 24 alkyl or alkenyl radical, A represents the ethylene or propylene radical and X is a -CO group or the direct bond.
- the compounds are in the form of their free bases or in protonated or quaternized form.
- R is preferably C 12 -C 24 alkyl or alkenyl, such as dodecyl, eexadecyl, octadecyl, octadecadienyl, arachinyl, behenyl, the alkyl groups (mixtures) of soybean fatty acids or tallow oils.
- m is preferably 1 to 3, especially 1.
- the sum xyz is preferably 15-80, especially 30-40, and the (AO) xyz chains are preferably of the ethylene glycol or ethylene-propylene-glycol type, preferably the former.
- the aforementioned compounds are preferably used as salts, optionally in quaternary form.
- Salts are, for example, those of the hydrohalic acids, for example the chlorides.
- Preferred quaternary salts are those which carry a C 1 -C 4 , alkyl or C 1 -C 4 alkylaryl group on the N atom, preferably the methyl or benzyl radical.
- anions are preferably Cl- or SO 4 - - .
- the preferred compounds are those of the general formula II (or salts thereof):
- the local application of the second approach containing the auxiliary means according to the invention takes place by means of printing systems of the type of stencil and / or rotary film printing, rotary relief printing or Spray pressure. Furthermore, spot-on sampling methods (known, for example, under the name TAK) and sampling methods for yarns (known, for example, under the name Space Deying) can be used according to the invention.
- spot-on sampling methods known, for example, under the name TAK
- sampling methods for yarns known, for example, under the name Space Deying
- the amounts of the auxiliaries to be used according to the invention in the second printing liquor or paste are about 1 to 15 g / 1, preferably 1 to 12 g / l, especially 4 to 8 g / l, based on the liquor or paste.
- the second approach contains a disperse and / or anion dye or corresponding brightener type.
- the anionic component (dye or brightener) must have at least one K value less than the first (for the fund coloring).
- Several pastes or liquors can also be applied simultaneously and one after the other.
- Preferred anionic dyes (or brighteners) have K values which are 2 to 6 lower than those for dyes in the fund coloring.
- Preferred anionic dyes are acid, metal complex or direct dyes, preferably acid dyes. All of these are known from the Color Index. Those of the Nyiosan E and N series are particularly preferred.
- the properties of the brighteners are said to be similar to those of the acid dyes.
- the second liquor can also contain conventional additives or auxiliaries such as thickeners.
- the pH of the liquor or paste is adjusted to 9-10, for example by weak alkalis (with a puffing effect) such as Na 3 PO 4 , Na 2 HPO 4 or the like; the additives must be compatible with alkali.
- the fixation takes place in a known manner by hot air or hot steam, preferably the latter, at 100-105 ° within 2-20, preferably 5-10 minutes.
- the washing and drying take place in a known and customary manner.
- the dyeing process according to the invention is a continuous process of the wet-on-wet type.
- the multicolor and reserve effects are sharp and pronounced, even with relatively small amounts of the alkoxylated fatty (poly) amines used according to the invention. This is particularly advantageous in carpet dyeing for reasons of energy and water savings.
- a reserve effect can also be achieved with a completely new dye range, and dyes that were previously unsuitable can now be used for this purpose.
- the process according to the invention is suitable in the broadest sense for fibers that can be dyed with anionic dyes, but especially for polyamides e.g. of natural origin, such as wool or silk, but especially for synthetic polyamide fibers, such as polyamide 6 or 66.
- the finished textile materials can be woven, knitted or tufted carpets, yarns and cables.
- a tufted carpet made of polyamide 66 is primed with a padding liquor of the following composition with a liquor absorption of 200%.
- the pH is adjusted to 5 with acetic acid.
- a fleet of the following composition is dripped onto the carpet primed in this way. For 1000 parts, this contains 15 parts of locust bean gum thickening (commercially available), 6 parts of aminopropyl tallowamine, 30-fold ethoxylated (reservation agent), 2 parts of trisodium phosphate.
- the carpet is treated with saturated steam at 100 ° for 10 minutes and then rinsed. A white patterned carpet with a brown background is obtained.
- Example 1 The procedure of Example 1 is followed, but a paint liquor is dripped on, which contains the following constituents (per 1000 parts): 3 parts of C.I. Acid Orange 156 (K 'value 2.5), 15 parts of locust bean gum thickening (commercially available), 6 parts of the auxiliary according to Example 1, 2 parts of trisodium phosphate.
- the carpet is steamed with saturated steam at 100 ° for 10 minutes and rinsed on it. It shows orange spots of good brilliance in the places of the applied drops.
- a knitted fabric made of polyamide 6 carpet yarn is primed with a liquor containing 1000 parts of 16 parts of CI Acid Green 106, otherwise according to the instructions in Example 1.
- the pick-up is 100%. It is then printed with a printing paste which contains the following constituents (per 1000) 3 parts of CI Acid Blue 40 (K 'value 2), 15 parts of locust beans Bread flour thickening (commercially available), 6 parts of the auxiliary according to Example 1, 2 parts of trisodium phosphate.
- a polyamide 6 loop carpet (Perlon type) is poured onto a pick-up by 120% with the following liquor (per 1000 parts): 12 parts CI Acid Green 106 (K 'value 8.5), 4 parts of ethereal thickener (commercial goods), 2 Share non-ionic emulsifier (commodity). The pH is adjusted to 6 (glacial acetic acid).
- the carpet treated in this way is partially printed with the following paste (per 1000 parts): 2.8 parts CI Acid Yellow 151 (K 'value 3), 2 parts CI Acid Yellow 127 (K' value 3.5), 2.8 parts CI Acid Orange 127 ( K 'value 3.5), 4 parts aminopropyl tallowamine, 30-fold ethoxylated, 15 parts alkali-resistant synthetic thickener, 1 part Na 3 PO 4 , 4 parts Na 2 HPO 4 .
- the carpet is then treated in saturated steam (100 °) for 10 minutes and then washed and dried. A yellow and orange pattern on a green background is obtained.
- the following dye mixture is used in the background: 2.2 parts of C.I. Acid Brown 298, 8.24 parts C.I. Acid Blue 80 (K'-value 9) and 0.7 parts C.I. Acid Green 106 and locally over-dyed with the following mixture: 2 parts C.I. Acid Orange (K 'value 2.5) and 0.4 parts C.I. Acid Blue 40 (K 'value 2). Equally good results are achieved.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Geology (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1149/79 | 1979-02-06 | ||
CH114979 | 1979-02-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1980001577A1 true WO1980001577A1 (en) | 1980-08-07 |
Family
ID=4203626
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CH1980/000009 WO1980001577A1 (en) | 1979-02-06 | 1980-01-29 | Resist printing process and means for its application |
Country Status (9)
Country | Link |
---|---|
US (2) | US4285691A (he) |
JP (1) | JPS55107588A (he) |
BE (1) | BE904563Q (he) |
CH (1) | CH660830GA3 (he) |
DE (1) | DE3003192C2 (he) |
FR (1) | FR2448595A1 (he) |
GB (1) | GB2043708B (he) |
IT (1) | IT1144053B (he) |
WO (1) | WO1980001577A1 (he) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0593392A1 (de) * | 1992-09-30 | 1994-04-20 | Ciba-Geigy Ag | Verfahren zum Färben von natürlichen und synthetischen Polyamidfasermaterialien mit Farbstoffmischungen |
WO1994023116A1 (de) * | 1993-04-02 | 1994-10-13 | Dlw-Aktiengesellschaft | Differentialdruck-verfahren |
EP0892105A1 (de) * | 1997-07-14 | 1999-01-20 | DLW Aktiengesellschaft | Verdrängungsdruckverfahren |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3222516C2 (de) * | 1981-06-25 | 1987-04-09 | Sandoz-Patent-GmbH, 7850 Lörrach | Reservedruckverfahren |
FR2611737B1 (fr) * | 1987-03-04 | 1993-07-23 | Sandoz Sa | Melanges de colorants anioniques pour la teinture de la laine |
DE3932869C2 (de) * | 1989-10-02 | 1996-03-21 | Zschimmer & Schwarz Gmbh & Co | Verwendung von Dialkylmonoaminalkoxylat-Verbindungen zum Reservieren von anionischen Färbungen auf Polyamidfasermaterial |
DE4219317A1 (de) * | 1991-06-17 | 1992-12-24 | Sandoz Ag | Faerbereihilfsmittel |
GB9120227D0 (en) * | 1991-09-23 | 1991-11-06 | Ici Plc | Printing process and pretreatment composition |
IT1261839B (it) * | 1992-08-03 | 1996-06-03 | Sandoz Ag | Procedimento per la produzione di effetti speciali di coloritura su prodotti tessili e miscele di coloranti impiegate. |
US5364417A (en) * | 1992-11-16 | 1994-11-15 | Milliken Research Corporation | Method of dyeing nylon fiber with acid dye: sullfamic acid |
US5478229A (en) * | 1993-01-29 | 1995-12-26 | The Japan Steel Works, Ltd. | Apparatus for forming hollow article |
JPH1046482A (ja) * | 1996-05-29 | 1998-02-17 | Ciba Specialty Chem Holding Inc | 天然及び合成ポリアミド繊維材料に防染性又は多色効果を与える方法 |
DE10109483A1 (de) * | 2001-02-28 | 2002-09-05 | Clariant Gmbh | Oxalkylierungsprodukte hergestellt aus Epoxiden und Aminen und deren Verwendung in Pigmentpräparationen |
US20050241077A1 (en) * | 2004-04-28 | 2005-11-03 | Soo Park H | Method of producing printed fabrics and the produced therefrom |
CN110192116B (zh) | 2017-01-25 | 2021-09-21 | 三菱电机株式会社 | 壳体及磁传感器装置 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2967755A (en) * | 1957-02-05 | 1961-01-10 | Sandoz Ltd | Leveling and stripping agents |
GB1006787A (en) * | 1963-01-05 | 1965-10-06 | Sandoz Ag | Improvements in or relating to polyoxyalkylated amine salts and process for the treatment of textile materials |
FR1567530A (he) * | 1967-05-26 | 1969-05-16 | ||
FR2046944A2 (en) * | 1969-06-20 | 1971-03-12 | Sandoz Sa | Polyamide textile mixed dyeing using acidic - dyes |
US4130589A (en) * | 1974-12-11 | 1978-12-19 | Sandoz Ltd. | Oxyalkylated alkyl polyamines as defoaming agents |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL102695C (he) * | 1955-11-28 | |||
US3074774A (en) * | 1959-10-16 | 1963-01-22 | Arkansas Company Inc | Discharge printing pastes and methods of application involving same |
ES367288A1 (es) * | 1968-05-17 | 1971-04-01 | Sandoz Ag | Procedimiento para tenir lana con colorantes reactivos. |
US3591325A (en) * | 1969-04-25 | 1971-07-06 | Arkansas Co Inc | Products and process for removing organic pigments and dyes from dyed and printed natural and synthetic textile materials |
CH544839A (de) * | 1970-05-22 | 1973-05-15 | Ciba Geigy Ag | Verfahren zur Erzeugung von Mehrton-Effekten auf Fasermaterial aus Polyacrylnitril oder Polyacrylnitrilcopolymeren |
DE2362741B2 (de) | 1973-12-17 | 1976-08-26 | Ausscheidung in: 23 65 814 Hoechst AG, 6000 Frankfurt | Verfahren zum erzielen von differenzierten farb- und fliesseffekten auf textilen flaechengebilden |
DE2424303C3 (de) | 1974-05-18 | 1983-12-01 | Hoechst Ag, 6230 Frankfurt | Verfahren zum Färben von Polyamid- Teppichmaterial nach einem Klotz-Kaltverweil-Verfahren |
DE2633615C3 (de) * | 1976-07-27 | 1981-08-13 | Bayer Ag, 5090 Leverkusen | Verfahren zum Färben von synthetischen Polyamid-Fasermaterialien |
-
1980
- 1980-01-28 IT IT47724/80A patent/IT1144053B/it active
- 1980-01-29 WO PCT/CH1980/000009 patent/WO1980001577A1/de unknown
- 1980-01-29 CH CH749680A patent/CH660830GA3/de unknown
- 1980-01-30 DE DE3003192A patent/DE3003192C2/de not_active Expired
- 1980-01-31 US US06/117,254 patent/US4285691A/en not_active Expired - Lifetime
- 1980-02-01 GB GB8003484A patent/GB2043708B/en not_active Expired
- 1980-02-04 JP JP1157380A patent/JPS55107588A/ja active Granted
- 1980-02-05 FR FR8002419A patent/FR2448595A1/fr active Granted
-
1981
- 1981-06-26 US US06/277,860 patent/US4411665A/en not_active Expired - Lifetime
-
1986
- 1986-04-09 BE BE1/011472A patent/BE904563Q/fr not_active IP Right Cessation
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2967755A (en) * | 1957-02-05 | 1961-01-10 | Sandoz Ltd | Leveling and stripping agents |
GB1006787A (en) * | 1963-01-05 | 1965-10-06 | Sandoz Ag | Improvements in or relating to polyoxyalkylated amine salts and process for the treatment of textile materials |
FR1567530A (he) * | 1967-05-26 | 1969-05-16 | ||
FR2046944A2 (en) * | 1969-06-20 | 1971-03-12 | Sandoz Sa | Polyamide textile mixed dyeing using acidic - dyes |
US4130589A (en) * | 1974-12-11 | 1978-12-19 | Sandoz Ltd. | Oxyalkylated alkyl polyamines as defoaming agents |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0593392A1 (de) * | 1992-09-30 | 1994-04-20 | Ciba-Geigy Ag | Verfahren zum Färben von natürlichen und synthetischen Polyamidfasermaterialien mit Farbstoffmischungen |
US5356445A (en) * | 1992-09-30 | 1994-10-18 | Ciba-Geigy Corporation | Process for dyeing natural or synthetic polyamide fibre material with dye mixtures |
WO1994023116A1 (de) * | 1993-04-02 | 1994-10-13 | Dlw-Aktiengesellschaft | Differentialdruck-verfahren |
EP0892105A1 (de) * | 1997-07-14 | 1999-01-20 | DLW Aktiengesellschaft | Verdrängungsdruckverfahren |
Also Published As
Publication number | Publication date |
---|---|
US4411665A (en) | 1983-10-25 |
FR2448595B1 (he) | 1983-06-24 |
JPS55107588A (en) | 1980-08-18 |
GB2043708A (en) | 1980-10-08 |
IT1144053B (it) | 1986-10-29 |
BE904563Q (fr) | 1986-07-31 |
US4285691A (en) | 1981-08-25 |
IT8047724A0 (it) | 1980-01-28 |
GB2043708B (en) | 1983-08-17 |
CH660830GA3 (he) | 1987-05-29 |
DE3003192A1 (de) | 1980-08-07 |
DE3003192C2 (de) | 1987-04-09 |
FR2448595A1 (fr) | 1980-09-05 |
JPS6316516B2 (he) | 1988-04-08 |
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