EP0302013A1 - Verfahren zum Färben von textilen Flächengebilden aus Polyamiden - Google Patents
Verfahren zum Färben von textilen Flächengebilden aus Polyamiden Download PDFInfo
- Publication number
- EP0302013A1 EP0302013A1 EP88810495A EP88810495A EP0302013A1 EP 0302013 A1 EP0302013 A1 EP 0302013A1 EP 88810495 A EP88810495 A EP 88810495A EP 88810495 A EP88810495 A EP 88810495A EP 0302013 A1 EP0302013 A1 EP 0302013A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dyes
- dye
- dyeing
- anionic
- sulfonic acid
- 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- Withdrawn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
- 238000000034 method Methods 0.000 title claims abstract description 31
- 238000004043 dyeing Methods 0.000 title claims abstract description 16
- 239000004952 Polyamide Substances 0.000 title claims abstract description 10
- 229920002647 polyamide Polymers 0.000 title claims abstract description 10
- 239000004753 textile Substances 0.000 title claims abstract description 8
- 239000004744 fabric Substances 0.000 title claims abstract description 5
- 239000000975 dye Substances 0.000 claims abstract description 56
- 125000000129 anionic group Chemical group 0.000 claims abstract description 16
- -1 melamine compound Chemical class 0.000 claims abstract description 13
- 230000002378 acidificating effect Effects 0.000 claims abstract description 10
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 8
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 8
- 230000003287 optical effect Effects 0.000 claims abstract description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 6
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract description 4
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims abstract description 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 4
- 125000005843 halogen group Chemical group 0.000 claims abstract description 3
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 16
- 210000002268 wool Anatomy 0.000 claims description 11
- 238000004040 coloring Methods 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000000987 azo dye Substances 0.000 claims description 4
- 238000005470 impregnation Methods 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 3
- 150000004056 anthraquinones Chemical class 0.000 claims description 3
- 230000000699 topical effect Effects 0.000 claims description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 15
- 239000002253 acid Substances 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- 229910052804 chromium Inorganic materials 0.000 description 6
- 239000000434 metal complex dye Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 150000003863 ammonium salts Chemical class 0.000 description 5
- 150000007974 melamines Chemical class 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 239000002657 fibrous material Substances 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000985 reactive dye Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 238000010186 staining Methods 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
- DWRLZGBQVFEEKS-UHFFFAOYSA-N 3-[[4,6-bis(3-sulfoanilino)-1,3,5-triazin-2-yl]amino]benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC(NC=2N=C(NC=3C=C(C=CC=3)S(O)(=O)=O)N=C(NC=3C=C(C=CC=3)S(O)(=O)=O)N=2)=C1 DWRLZGBQVFEEKS-UHFFFAOYSA-N 0.000 description 2
- 229920000161 Locust bean gum Polymers 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 150000004700 cobalt complex Chemical class 0.000 description 2
- 230000009918 complex formation Effects 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000000711 locust bean gum Substances 0.000 description 2
- 235000010420 locust bean gum Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-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
- MRERMGPPCLQIPD-NBVRZTHBSA-N (3beta,5alpha,9alpha,22E,24R)-3,5,9-Trihydroxy-23-methylergosta-7,22-dien-6-one Chemical compound C1C(O)CCC2(C)C(CCC3(C(C(C)/C=C(\C)C(C)C(C)C)CCC33)C)(O)C3=CC(=O)C21O MRERMGPPCLQIPD-NBVRZTHBSA-N 0.000 description 1
- KZMAWJRXKGLWGS-UHFFFAOYSA-N 2-chloro-n-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-n-(3-methoxypropyl)acetamide Chemical compound S1C(N(C(=O)CCl)CCCOC)=NC(C=2C=CC(OC)=CC=2)=C1 KZMAWJRXKGLWGS-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- FBWSRAOCSJQZJA-UHFFFAOYSA-N 4-iminonaphthalen-1-one Chemical compound C1=CC=C2C(=N)C=CC(=O)C2=C1 FBWSRAOCSJQZJA-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
- 240000008886 Ceratonia siliqua Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 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
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- PDWCVHGVTVOSIE-UHFFFAOYSA-N [nitro(diphenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)([N+](=O)[O-])C1=CC=CC=C1 PDWCVHGVTVOSIE-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
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
- 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
-
- 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
-
- 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
- D06P1/62—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 low-molecular-weight organic compounds with sulfate, sulfonate, sulfenic or sulfinic groups
- D06P1/628—Compounds containing nitrogen
-
- 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
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/917—Wool or silk
-
- 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
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/924—Polyamide fiber
Definitions
- the amount of the melamine compound depends in particular on the amount of dye used and the desired reserve or colored print, an amount of 50 to 150 g per liter of reserve preparation having proven to be advantageous.
- the melamine compound advantageously contains 1 to 4, preferably 2 to 3 acidic water-solubilizing groups, which can in particular be carboxyl or sulfonic acid groups.
- a melamine compound can contain only carboxyl groups or only sulfonic acid groups as well as both carboxyl and sulfo groups.
- R1, R2 and R3 may be the same or different.
- R1, R2 and R3 each represent phenyl.
- the melamine compounds used in the process according to the invention are known per se or can be prepared by methods known per se.
- the melamine compounds used in the process according to the invention are either in the form of the free acid or preferably as their salts.
- suitable salts are the alkali metal, alkaline earth metal or ammonium salts or the salts of an organic amine.
- Examples include the sodium, potassium or ammonium salts or the salt of triethanolamine.
- anionic dyes used for the process according to the invention are known from the Color Index. Basically all anionic dyes are suitable.
- the anionic dyes are, for example, salts of heavy metal-containing or metal-free mono-, dis- or polyazo dyes including the formazan dyes and the anthraquinone, xanthene, nitro, triphenylmethane, naphthoquinoneimine and phthalocyanine dyes.
- the anionic character of these dyes can be caused by metal complex formation alone and / or preferably by acidic, salt-forming substituents, such as carboxylic acid groups, sulfuric acid and phosphophonic acid ester groups, phosphonic acid groups or sulfonic acid groups.
- These dyes can also have so-called reactive groups in the molecule, which form a covalent bond with the material to be colored. Acidic, metal-free dyes or reactive dyes which have a single sulfonic acid group and which preferably have at least two sulfonic acid groups are preferred.
- the 1: 1 metal complex dyes preferably have one or two sulfonic acid groups. As metal, they contain a heavy metal atom, such as copper, nickel or, in particular, chromium.
- the 1: 2 metal complex dyes contain a heavy metal atom as the central atom, such as a cobalt atom or in particular a chromium atom.
- Two complex-forming components are connected to the central atom, at least one of which is a dye molecule, but preferably both are dye molecules. The two dye molecules involved in the complex formation can be the same or different from one another.
- the 1: 2 metal complex dyes can, for example, two azomethine molecules, one Disazo dye and a monoazo dye or preferably contain two monoazo dye molecules.
- the azo dye molecules can have water-solubilizing groups such as acid amide, alkylsulfonyl or the above acidic groups. Preference is given to 1: 2 cobalt or 1: 2 chromium complexes of monoazo dyes which have acid amide groups, alkylsulfonyl groups or a total of a single sulfonic acid group.
- anionic dyes can also be used.
- dye mixtures of at least 2 or 3 anionic dyes can be used.
- the amount of dyes used depends on the desired depth of color of the reserve and color printing. In general, amounts of 0.02 to 10 percent by weight, in particular 0.05 to 5 percent by weight, based on the fiber material used, have proven successful.
- anionic optical brighteners can also be used.
- synthetic polyamide silk or especially wool alone or mixtures of wool and polyamide are to be mentioned.
- the synthetic polyamide comes e.g. that from adipic acid and hexamethylenediamine (polyamide 6,6), from ⁇ -caprolactam (polyamide 6), from ⁇ -aminoundecanoic acid (polyamide 11), from ⁇ -aminoonanthic acid (polyamide 7), from ⁇ -amino-pelargonic acid (polyamide 8) or from sebacic acid and hexamethylenediamine (polyamide 6.10).
- the fiber materials are flat, especially floor coverings, such as Carpet or other home textiles such as upholstery fabrics, curtains or wall coverings.
- Both the preparations for topical application of the reservation agent alone or in combination with the dye or optical brightener and the dyeing liquors for overdyeing advantageously contain mineral acids, such as sulfuric acid or phosphoric acid, or organic acids, such as formic acid, acetic acid, oxalic acid or preferably citric acid . You can also use salts like Contain ammonium acetate, ammonium sulfate or sodium acetate. The acids are used primarily to adjust the pH of the preparations or liquors, which is usually 3 to 7, preferably 3.5 to 4.5.
- the dyes or optical brighteners In addition to the melamine compounds (reservation agents), the dyes or optical brighteners, other auxiliaries customary in dyeing technology can also be used. They are e.g. Dispersing agents, leveling agents, electrolytes, wetting agents, defoamers, anti-foaming agents, thickeners or wool protection agents.
- the reserve print or the local coloration is done according to the usual methods for printing. They can be done using drops, pressure rollers or stencils. This local application can be carried out on dry or pre-wetted goods. It is advantageous to use real dyes such as reactive and / or metal complex dyes for the local coloring.
- the heat treatment after the reservation or local coloring is usually carried out with saturated steam at 100-105 ° C or hot air at 120-160 ° C for pre-fixing and generally takes 5 to 20 minutes, preferably 7 to 15 minutes when using saturated steam and 60 to 120 seconds with hot air. After this pre-fixation, the over-staining takes place to produce the background staining.
- the dyeing is preferably carried out using acid dyes, which generally have migration properties.
- the background coloring can be produced by the exhaust process, impregnation process, continuously or semi-continuously, or also by printing.
- the impregnation can be applied e.g. Spray, splash or pour the dye liquor.
- the liquor ratio can be selected within a wide range, for example 1: 3 to 1: 100, preferably 1:10 to 1:40. It is convenient to work at a temperature of 30 to 98 ° C, preferably 50 to 70 ° C.
- the liquor application is expediently 250 to 800% by weight.
- the goods are then subjected to a second heat treatment process in order to fix the applied dyes. This fixation can also be carried out using the cold dwell method.
- the heat treatment is preferably carried out by a steaming process with treatment in a steamer with possibly superheated steam at a temperature of 98 to 105 ° C.
- the dyes can be fixed in accordance with the cold residence process by storing the impregnated and preferably rolled-up goods at room temperature (15 to 30 ° C) e.g. during 3 to 24 hours, the cold residence time being known to depend on the dye.
- the dyeings produced are washed and dried in the customary manner.
- the process according to the invention enables fiber material of the same quality to be dyed in a simple manner in different shades of color, which is of great importance particularly in the production of carpets because carpets can be produced which show a balanced picture with regard to the stability and gloss of the pile.
- the process is also economical because there is usually no need for intermediate washing and / or drying and expensive storage of large quantities of pre-colored material.
- a wool cut pile carpet which is locally printed as described in Example 2 (a), is impregnated on a fleet applicator with a fleet application of 400% with an aqueous dye liquor which contains 0.12 g of a dye of the formula (101) in liters. 0.045 g of a dye of the formula (102), 0.085 g of a dye of the formula (103), 1 g of the mixture of coconut fatty acid diethanolamide and the ammonium salt of the acid sulfuric acid ester of the adduct of 3 moles of ethylene oxide and 1 mole of lauryl alcohol (1: 1.7) and Contains 2 g locust bean gum thickener (commercially available) and adjusted to pH 4 with citric acid. The goods are then steamed for 10 minutes with saturated steam at 100 ° C. The pattern shows a yellow tone on a beige basic tone in the printed areas.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH2862/87 | 1987-07-27 | ||
CH286287 | 1987-07-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0302013A1 true EP0302013A1 (de) | 1989-02-01 |
Family
ID=4243256
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88810495A Withdrawn EP0302013A1 (de) | 1987-07-27 | 1988-07-19 | Verfahren zum Färben von textilen Flächengebilden aus Polyamiden |
Country Status (6)
Country | Link |
---|---|
US (1) | US4859207A (enrdf_load_stackoverflow) |
EP (1) | EP0302013A1 (enrdf_load_stackoverflow) |
JP (1) | JPS6445882A (enrdf_load_stackoverflow) |
KR (1) | KR890002488A (enrdf_load_stackoverflow) |
AU (1) | AU602783B2 (enrdf_load_stackoverflow) |
NZ (1) | NZ225548A (enrdf_load_stackoverflow) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0874081A1 (en) * | 1997-04-24 | 1998-10-28 | Basf Corporation | Dyeing articles composed of melamine and aramid fibers |
EP0874080A1 (en) * | 1997-04-24 | 1998-10-28 | Basf Corporation | Dyeing articles composed of melamine fiber and cellulose fiber |
RU2131953C1 (ru) * | 1996-07-17 | 1999-06-20 | Товарищество с ограниченной ответственностью "Институт технических сукон" | Способ изготовления маркированного игрального сукна |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4989213A (en) * | 1989-10-30 | 1991-01-29 | Polaroid Corporation | Narrow divergence, single quantum well, separate confinement, algaas laser |
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 |
US6524492B2 (en) | 2000-12-28 | 2003-02-25 | Peach State Labs, Inc. | Composition and method for increasing water and oil repellency of textiles and carpet |
US20020124323A1 (en) * | 2001-01-09 | 2002-09-12 | Cliver James D. | Process for patterning textile materials and fabrics made therefrom |
CN104015510B (zh) * | 2014-06-06 | 2016-09-07 | 无锡贝旭环球电子商务有限公司 | 一种使涤纶毛毯绒面印花具有3d效果的生产方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3097911A (en) * | 1963-07-16 | Process of reserving wool with bis-tri- | ||
DE1290519B (de) * | 1962-08-22 | 1969-03-13 | Hoechst Ag | Verfahren zum streifenfreien Faerben von Textilmaterialien aus Polyamiden |
DE1619548A1 (de) * | 1967-09-09 | 1971-02-11 | Hoechst Ag | Verfahren zum Faerben von Textilmaterialien aus Polyamidfasern mit kationischen Farbstoffen |
DE1769702A1 (de) * | 1967-07-03 | 1971-09-02 | Sandoz Ag | Verfahren zum Reservieren von Fasermaterial aus natuerlichen Polyamiden oder mit sauren Farbstoffen anfaerbbaren synthetischen Materialien |
DE2244060A1 (de) * | 1972-09-08 | 1974-03-28 | Hoechst Ag | Verfahren zum gleichmaessigen faerben von polyamidmaterialien |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH942967A4 (enrdf_load_stackoverflow) * | 1967-07-03 | 1972-03-30 |
-
1988
- 1988-07-19 EP EP88810495A patent/EP0302013A1/de not_active Withdrawn
- 1988-07-19 US US07/221,401 patent/US4859207A/en not_active Expired - Fee Related
- 1988-07-25 NZ NZ225548A patent/NZ225548A/xx unknown
- 1988-07-26 KR KR1019880009382A patent/KR890002488A/ko not_active Withdrawn
- 1988-07-26 AU AU20016/88A patent/AU602783B2/en not_active Ceased
- 1988-07-27 JP JP63185703A patent/JPS6445882A/ja active Granted
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3097911A (en) * | 1963-07-16 | Process of reserving wool with bis-tri- | ||
DE1290519B (de) * | 1962-08-22 | 1969-03-13 | Hoechst Ag | Verfahren zum streifenfreien Faerben von Textilmaterialien aus Polyamiden |
DE1769702A1 (de) * | 1967-07-03 | 1971-09-02 | Sandoz Ag | Verfahren zum Reservieren von Fasermaterial aus natuerlichen Polyamiden oder mit sauren Farbstoffen anfaerbbaren synthetischen Materialien |
DE1619548A1 (de) * | 1967-09-09 | 1971-02-11 | Hoechst Ag | Verfahren zum Faerben von Textilmaterialien aus Polyamidfasern mit kationischen Farbstoffen |
DE2244060A1 (de) * | 1972-09-08 | 1974-03-28 | Hoechst Ag | Verfahren zum gleichmaessigen faerben von polyamidmaterialien |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2131953C1 (ru) * | 1996-07-17 | 1999-06-20 | Товарищество с ограниченной ответственностью "Институт технических сукон" | Способ изготовления маркированного игрального сукна |
EP0874081A1 (en) * | 1997-04-24 | 1998-10-28 | Basf Corporation | Dyeing articles composed of melamine and aramid fibers |
EP0874080A1 (en) * | 1997-04-24 | 1998-10-28 | Basf Corporation | Dyeing articles composed of melamine fiber and cellulose fiber |
US5885307A (en) * | 1997-04-24 | 1999-03-23 | Basf Corporation | Dyeing articles composed of melamine fiber and cellulose fiber |
US5891813A (en) * | 1997-04-24 | 1999-04-06 | Basf Corporation | Articles having a chambray appearance and process for making them |
CN1107139C (zh) * | 1997-04-24 | 2003-04-30 | 美国Basf公司 | 对耐热及抗燃纤维进行染色的方法及耐热抗燃条纹织物 |
Also Published As
Publication number | Publication date |
---|---|
US4859207A (en) | 1989-08-22 |
AU2001688A (en) | 1989-01-27 |
NZ225548A (en) | 1989-11-28 |
AU602783B2 (en) | 1990-10-25 |
KR890002488A (ko) | 1989-04-10 |
JPS6445882A (en) | 1989-02-20 |
JPH0470430B2 (enrdf_load_stackoverflow) | 1992-11-10 |
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