US2501184A - Method of dyeing keratinous fibers - Google Patents
Method of dyeing keratinous fibers Download PDFInfo
- Publication number
- US2501184A US2501184A US529860A US52986044A US2501184A US 2501184 A US2501184 A US 2501184A US 529860 A US529860 A US 529860A US 52986044 A US52986044 A US 52986044A US 2501184 A US2501184 A US 2501184A
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- fibre
- acid
- dye
- aforesaid
- opening
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- Expired - Lifetime
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- 239000000835 fiber Substances 0.000 title claims description 40
- 238000000034 method Methods 0.000 title claims description 9
- 238000004043 dyeing Methods 0.000 title description 9
- 239000002253 acid Substances 0.000 claims description 21
- 239000000975 dye Substances 0.000 claims description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 12
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 10
- 239000003153 chemical reaction reagent Substances 0.000 claims description 10
- 102000011782 Keratins Human genes 0.000 claims description 6
- 108010076876 Keratins Proteins 0.000 claims description 6
- 230000008961 swelling Effects 0.000 claims description 6
- 239000004202 carbamide Substances 0.000 claims description 5
- 230000035699 permeability Effects 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- -1 guanadine Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 210000002268 wool Anatomy 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 235000011054 acetic acid Nutrition 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000036760 body temperature Effects 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical class CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000000982 direct dye Substances 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 210000004209 hair Anatomy 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
- MHIHRIPETCJEMQ-UHFFFAOYSA-N 2-nitrobutan-1-ol Chemical compound CCC(CO)[N+]([O-])=O MHIHRIPETCJEMQ-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
- 239000005711 Benzoic acid Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229940106008 d&c brown no. 1 Drugs 0.000 description 1
- AOMZHDJXSYHPKS-UHFFFAOYSA-L disodium 4-amino-5-hydroxy-3-[(4-nitrophenyl)diazenyl]-6-phenyldiazenylnaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(N=NC=3C=CC=CC=3)C(O)=C2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 AOMZHDJXSYHPKS-UHFFFAOYSA-L 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229960004592 isopropanol Drugs 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- YNTOKMNHRPSGFU-UHFFFAOYSA-N n-Propyl carbamate Chemical compound CCCOC(N)=O YNTOKMNHRPSGFU-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical class CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 229940080818 propionamide Drugs 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- ZQZJKHIIQFPZCS-UHFFFAOYSA-N propylurea Chemical compound CCCNC(N)=O ZQZJKHIIQFPZCS-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- VRDAELYOGRCZQD-NFLRKZIHSA-M sodium;4-[(2z)-2-[(5e)-5-[(2,4-dimethylphenyl)hydrazinylidene]-4,6-dioxocyclohex-2-en-1-ylidene]hydrazinyl]benzenesulfonate Chemical compound [Na+].CC1=CC(C)=CC=C1N\N=C(/C(=O)C=C\1)C(=O)C/1=N\NC1=CC=C(S([O-])(=O)=O)C=C1 VRDAELYOGRCZQD-NFLRKZIHSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct 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
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/6422—Compounds containing nitro or nitroso 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
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/645—Aliphatic, araliphatic or cycloaliphatic compounds containing amino 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
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/649—Compounds containing carbonamide, thiocarbonamide or guanyl 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
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/649—Compounds containing carbonamide, thiocarbonamide or guanyl groups
- D06P1/6491—(Thio)urea or (cyclic) derivatives
-
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/649—Compounds containing carbonamide, thiocarbonamide or guanyl groups
- D06P1/6492—(Thio)urethanes; (Di)(thio)carbamic acid derivatives; Thiuramdisulfide
-
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/649—Compounds containing carbonamide, thiocarbonamide or guanyl groups
- D06P1/6495—Compounds containing carbonamide -RCON= (R=H or hydrocarbons)
-
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/651—Compounds without nitrogen
- D06P1/65106—Oxygen-containing compounds
- D06P1/65118—Compounds containing hydroxyl 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
- 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
- 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
- D06P3/14—Wool
-
- 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
- D06P3/30—Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts
-
- 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
Definitions
- This invention relates to methods or media for dyeing keratinous fibres such as hair, wool, fur, feathers, etc, being particularly directed to the dyeing of these resistant fibres at low temperatures, as for example, in the range of human body tolerance.
- fibres such as wool
- dilute solutions of strong acids at high temperatures or concentrated solutions of certain weak acids at room temperature but in either event, the conditions of these treatments make them impractical for such use with resistant fibre of the class in the temperature range aforesaid, by virtue of their corrosive action in proximity of human tissue.
- the acid medium referred to above can be defined as a non-reducing weak acid or acid salt having a dissociation constant of 10- to 1G
- acid media having these properties which we have found useful in our method of dyeing, acetic acid, formic acid, propionic acid, tartaric acid, disodium hydrogen phosphate, malic acid, lactic acid, all of which are representative of the class defined aforesaid. Effective concentration of these acids or acid salts useful for dyeing purposes, in accordance with our discovery is from 1 to 15%.
- urea and its derivatives such as methyl-urea, propyl-urea, thio-urea, etc.
- carbamates and their derivatives such as urethane and propyl-carbamate, etc.
- amides and their derivatives such as formamide, acetamide, propionamide, etc.; salts of amines, such as guanadine, amylamine and butylamine, salts, etc; nitro-paraffines and their derivatives, such as nitro-methane, 2-nitro-1-propano1, 2- nitro-l-butanol, etc.; primary aliphatic alcohols, such as methyl, ethyl and iso-propyl alcohol; phenols, such as resorcinol, etc.; catechols, etc.
- the aforesaid water soluble organic reagents are usually applied in concentrations of 10 to 60%.
- nitro-paraifine series listed among the water soluble organic compounds are all effective as swelling agents acting on Opening fibres and are useful in association with weak acids under our procedure aforesaid, certain members of this group, namely Z-nitro-l-propanol and 2- :nitro-l-butanol, exemplifying nitro-paraifines having a labile hydrogen have been found to possess the properties by themselves of sufficiently opening keratin fibre to an extent that normally non-substantive dyes will be carried into the fibre for reaction therewith and deposit therein.
- a method for imparting color to keratinous fibre at body tolerance temperatures, with dyes normally non-substantive thereto which comprises treating the fibre with reagents incorporating a dye of the class aforesaid, said reagents consisting of dilute acetic acid having the characteristics of opening the fibre, and urea having the property of greatly swelling the keratin fibre and disrupting the secondary linkages thereof onl in the presence of and upon opening of th fibre by said acid, to increase the permeability of the fibre to the extent that the dye aforesaid penetrates and diffuses through the cuticle of the fibre.
- a method for imparting color to keratinous 4 fibre at body tolerance temperatures, with dyes normally non-substantive thereto which comprises treating the fibre with reagents incorporating a dye of the class aforesaid, said reagents consisting of dilute acetic acid having the characteristics of openin the fibre, and a mixture of urea and alcohol having the property of greatly swelling the keratin fibre and disrupting the secondary linkages thereof only in the presence of and upon opening of the fibre by said acid, to increase the permeability of the fibre to the extent that the dye aforesaid penetrates and diffuses through the cuticle of the fibre.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Coloring (AREA)
Description
Patented Mar. 21, 1950 METHOD F DYEING KERATINOUS FIBERS Edwin E. Michaels, Stamford, Conn., and Bernard Berk, New York, N. Y., assignors to Lawrence Richard Bruce, Incorporated, Stamford, Conn, a corporation of Connecticut No Drawing. Application April 6, 1944, Serial No. 529,860
2 Claims.
This invention relates to methods or media for dyeing keratinous fibres such as hair, wool, fur, feathers, etc, being particularly directed to the dyeing of these resistant fibres at low temperatures, as for example, in the range of human body tolerance.
Broadly, it is an object of this invention to provide for the dyeing of a resistant fibre of the character and within the range outlined aforesaid, by applying with and as a carrier for the dye, a composition incorporating respectively a medium, being or having the properties of a weak acid having the function of effecting a primary opening of the fibre, and a Water soluble organic medium functioning only in the presence of the first medium to effectuate a secondary opening of the fibre, thereby to increase the permeability of the fibre for the dyestufi.
Up to the present time, it has been known that fibres, such as wool, may be dyed upon treatment with dilute solutions of strong acids at high temperatures or concentrated solutions of certain weak acids at room temperature, but in either event, the conditions of these treatments make them impractical for such use with resistant fibre of the class in the temperature range aforesaid, by virtue of their corrosive action in proximity of human tissue.
In the prior art, particularly in the dyeing of textiles such as cotton or wool, certain water soluble organic compounds classified as dye assistants have been used to increase the solubility of normally slightly soluble dyes but such effect is of no avail in the treatment of keratinous fibre within the required body temperature range, in view of the resistance of the protein formation thereof to penetration.
We have found that weak acids of relatively low concentration and having a low dissociation constant when applied to a keratinous fibre at body temperature will react with the fibre to a high degree. This phenomenon may be explained by the Proctor-Wilson theory of swelling. Use has been made of the high degree of reaction of weak acids with keratinous fibres to a limited extent for imparting a surface coloration thereto by reacting dyestuff with these acids for absorption on the surface of the fibre. However, this limited opening of the fibre in the presence of dilute solutions of weak acids per se is not enough to permit the entrance of dye molecules to the fibres and the end product obtained by this step is a temporary soap fugitive surface coloration.
We have, as an object of this invention discovered that use can be made of the phenomenon involving the reaction of the weak acid with the keratin, for slightly opening the same to make accessible to the fibre a second group of reagents, namely, water soluble compounds of a class, which under the above condition acting on the slightly opened fibre by greatly swelling the same disrupting the secondary linkages thereof and further opening its pores to such an extent that normally non-substantive dye will be carried into the fibre for reaction therewith and deposit therein, to thereby dye the cuticle and cortex of the fibre and permanently coloring the keratin in such a manner as is useful for commercial processes.
The acid medium referred to above can be defined as a non-reducing weak acid or acid salt having a dissociation constant of 10- to 1G As examples of acid media having these properties which we have found useful in our method of dyeing, acetic acid, formic acid, propionic acid, tartaric acid, disodium hydrogen phosphate, malic acid, lactic acid, all of which are representative of the class defined aforesaid. Effective concentration of these acids or acid salts useful for dyeing purposes, in accordance with our discovery is from 1 to 15%.
Among the class of water soluble organic compound, we have found that the most useful in the effectuation of our procedure are: urea and its derivatives such as methyl-urea, propyl-urea, thio-urea, etc.; carbamates and their derivatives, such as urethane and propyl-carbamate, etc. amides and their derivatives such as formamide, acetamide, propionamide, etc.; salts of amines, such as guanadine, amylamine and butylamine, salts, etc; nitro-paraffines and their derivatives, such as nitro-methane, 2-nitro-1-propano1, 2- nitro-l-butanol, etc.; primary aliphatic alcohols, such as methyl, ethyl and iso-propyl alcohol; phenols, such as resorcinol, etc.; catechols, etc. The aforesaid water soluble organic reagents are usually applied in concentrations of 10 to 60%.
Following is a representative example of a treatment solution applicable in accordance With our invention to dye keratinous fibre, for instance, human hair, to a medium brown color.
We dissolve a mixture of dyes of the following proportion:
.6 gr. D & C Black No. 1 .5 gr. D & C Brown No. 1 .4 gr. External D & C Red #13 We may, for the purpose of increasing the ease of dissolving the dyestufi and contributing to its stability in the acid solution incorporate as part of the solvent a wetting agent such as those readily purchasable on the market under various trade-marks and of 1% benzoic acid.
Although in the aforesaid example we have indicated the use of a single water soluble organic reagent in association with the weak acid, we may apply an intermixture of more than one such reagent, as for example, we have successfully applied the following mixture in association with the dyestufi and the acid of Example 1. In lieu of urea we have used 20% urethane and ethyl alcohol.
Although the nitro-paraifine series listed among the water soluble organic compounds are all effective as swelling agents acting on Opening fibres and are useful in association with weak acids under our procedure aforesaid, certain members of this group, namely Z-nitro-l-propanol and 2- :nitro-l-butanol, exemplifying nitro-paraifines having a labile hydrogen have been found to possess the properties by themselves of sufficiently opening keratin fibre to an extent that normally non-substantive dyes will be carried into the fibre for reaction therewith and deposit therein.
Various changes and modifications may be made to the details of the invention without departing from the broader spirit and scope thereof, as set forth in the following claims.
We claim:
1. A method for imparting color to keratinous fibre at body tolerance temperatures, with dyes normally non-substantive thereto, which comprises treating the fibre with reagents incorporating a dye of the class aforesaid, said reagents consisting of dilute acetic acid having the characteristics of opening the fibre, and urea having the property of greatly swelling the keratin fibre and disrupting the secondary linkages thereof onl in the presence of and upon opening of th fibre by said acid, to increase the permeability of the fibre to the extent that the dye aforesaid penetrates and diffuses through the cuticle of the fibre.
2. A method for imparting color to keratinous 4 fibre at body tolerance temperatures, with dyes normally non-substantive thereto, which comprises treating the fibre with reagents incorporating a dye of the class aforesaid, said reagents consisting of dilute acetic acid having the characteristics of openin the fibre, and a mixture of urea and alcohol having the property of greatly swelling the keratin fibre and disrupting the secondary linkages thereof only in the presence of and upon opening of the fibre by said acid, to increase the permeability of the fibre to the extent that the dye aforesaid penetrates and diffuses through the cuticle of the fibre.
EDWIN B. MICHAELS.
BERNARD BERK.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,886,412 Martin Nov. 8, 1932 2,018,436 Brandt Oct. 22, 1935 2,116,521 Kritchevsky May 10, 1938 2,163,043 Kritchevsky June 20, 1939 2,183,754 Schlack Dec. 19, 1939 2,185,467 Kritchevsky Jan. 2, 1940 2,228,369 Schoeller Jan 14, 1941 2,238,949 Schlack Apr. 22, 1941 2,261,094 Speakman Oct. 28, 1941 2,303,932 Guild Dec. 1, 1942 FOREIGN PATENTS Number Country Date 44,949 France May 1, 1935 (1st addition to No. 771,270) 453,559 Great Britain 1935 828,616 France May 24, 1938 OTHER REFERENCES Jones and Mechan, Dispersion of Kcratins, Archives of Bio-Chemistry, vol. 2 (1943), pages 209-223.
Goodall Theory of Wool Dyeing, Soc. of Dyers and Colourists, February 1937, pages 5056.
Claims (1)
1. A METHOD FOR IMPARTING COLOR TO KERATINOUS FIBRE AT BODY TOLERANCE TEMPERATURES, WITH DYES NORMALLY NON-SUBSTANTIVE THERETO, WHICH COMPRISES TREATING THE FIBRE WITH REAGENTS INCORPORATING A DYE OF THE CLASS AFORESAID, SAID REAGENTS CONSISTING OF DILUTE ACETIC ACID HAVING THE CHARACTERISTICS OF OPENING THE FIBRE, AND UREA HAVING THE PROPERTY OF GREATLY SWELLING THE KERATIN FIBRE AND DISRUPTING THE SECONDARY LINKAGES THEREOF ONLY IN THE PRESENCE OF AND UPON OPENING OF THE FIBRE BY SAID ACID, TO INCREASE THE PERMEABILITY OF THE FIBRE TO THE EXTENT THAT THE DYE AFORESAID PENETRATES AND DIFFUSES THROUGH THE CUTICLE OF THE FIBRE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US529860A US2501184A (en) | 1944-04-06 | 1944-04-06 | Method of dyeing keratinous fibers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US529860A US2501184A (en) | 1944-04-06 | 1944-04-06 | Method of dyeing keratinous fibers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2501184A true US2501184A (en) | 1950-03-21 |
Family
ID=24111538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US529860A Expired - Lifetime US2501184A (en) | 1944-04-06 | 1944-04-06 | Method of dyeing keratinous fibers |
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| Country | Link |
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| US (1) | US2501184A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2643211A (en) * | 1949-11-30 | 1953-06-23 | Rayette Inc | Hair color-rinse concentrate |
| DE920388C (en) * | 1950-06-30 | 1954-11-22 | Warner Hudnut | Hair treatment preparations |
| US2717228A (en) * | 1951-04-23 | 1955-09-06 | Gillette Co | Hair waving composition |
| US2776668A (en) * | 1951-06-28 | 1957-01-08 | Rubinstein Inc H | Method and preparations for the permanent dyeing of keratinous material |
| US2890094A (en) * | 1955-11-21 | 1959-06-09 | Jos H Lowenstein & Sons Inc | Dyeing composition and method |
| DE974422C (en) * | 1951-11-22 | 1960-12-22 | Hoechst Ag | Means for the permanent deformation of scleroproteins, especially hair |
| US3100739A (en) * | 1958-02-25 | 1963-08-13 | Therachemie Chem Therapeut | Process for dyeing human hair with water soluble, quaternary ammonium containing dyes |
| US3215605A (en) * | 1962-04-25 | 1965-11-02 | Revlon | Method for coloring hair and other keratinaceous fibers with metal salts |
| US3261754A (en) * | 1956-04-21 | 1966-07-19 | Rapidol Ltd | Solvent dyeing of human hair |
| US3521989A (en) * | 1966-10-04 | 1970-07-28 | Commw Scient Ind Res Org | Method of dyeing wool and composition therefor |
| US4169706A (en) * | 1975-07-18 | 1979-10-02 | Ernst Kruchen | Method of cleaning poultry feathers |
| US5705030A (en) * | 1993-12-29 | 1998-01-06 | The United States Of America As Represented By The Secretary Of Agriculture | Fiber and fiber products produced from feathers |
| US6436380B1 (en) | 1992-12-31 | 2002-08-20 | Advantage Partners Llc | Baldness cosmetic and method of application |
| EP1454614A1 (en) * | 2003-03-06 | 2004-09-08 | KPSS-Kao Professional Salon Services GmbH | Composition for dyeing human hair |
| US6814957B1 (en) | 1992-12-31 | 2004-11-09 | Kenneth Pond | Baldness cosmetic and method of application |
| US20040231069A1 (en) * | 2003-03-06 | 2004-11-25 | Kpss-Kao Professional Salon Services Gmbh | Composition for dyeing human hair |
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| US2018436A (en) * | 1932-05-12 | 1935-10-22 | Firm Durand & Huguenin S A | Printing of animal fibers with mordant dyestuffs |
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| US2116521A (en) * | 1934-05-07 | 1938-05-10 | Rit Products Corp | Hair dyeing method and composition |
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| US2261094A (en) * | 1934-12-10 | 1941-10-28 | Speakman John Bamber | Treatment of keratins |
| US2303932A (en) * | 1940-03-02 | 1942-12-01 | Bruno T Guild | Personal cleaning composition |
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| US1886412A (en) * | 1929-08-02 | 1932-11-08 | Gaudit Jules Martin Dit | Dyeing and printing process |
| US2018436A (en) * | 1932-05-12 | 1935-10-22 | Firm Durand & Huguenin S A | Printing of animal fibers with mordant dyestuffs |
| US2228369A (en) * | 1933-12-20 | 1941-01-14 | Gen Aniline & Film Corp | Dyeing animal fibrous materials |
| US2116521A (en) * | 1934-05-07 | 1938-05-10 | Rit Products Corp | Hair dyeing method and composition |
| GB453559A (en) * | 1934-12-03 | 1936-09-03 | John Bamber Speakman | Improvements in the process for permanently waving keratin containing fibres |
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| US2238949A (en) * | 1936-02-06 | 1941-04-22 | Process of modifying the electro | |
| FR828616A (en) * | 1936-11-03 | 1938-05-24 | Ig Farbenindustrie Ag | Adjuvants for use in dyeing and dyeing process using substantive dyes |
| US2163043A (en) * | 1938-02-07 | 1939-06-20 | Rit Products Corp | Hair dyeing composition and method |
| US2185467A (en) * | 1938-10-03 | 1940-01-02 | Rit Products Corp | Hair dyeing composition and method |
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Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2643211A (en) * | 1949-11-30 | 1953-06-23 | Rayette Inc | Hair color-rinse concentrate |
| DE920388C (en) * | 1950-06-30 | 1954-11-22 | Warner Hudnut | Hair treatment preparations |
| US2717228A (en) * | 1951-04-23 | 1955-09-06 | Gillette Co | Hair waving composition |
| US2776668A (en) * | 1951-06-28 | 1957-01-08 | Rubinstein Inc H | Method and preparations for the permanent dyeing of keratinous material |
| DE974422C (en) * | 1951-11-22 | 1960-12-22 | Hoechst Ag | Means for the permanent deformation of scleroproteins, especially hair |
| US2890094A (en) * | 1955-11-21 | 1959-06-09 | Jos H Lowenstein & Sons Inc | Dyeing composition and method |
| US3261754A (en) * | 1956-04-21 | 1966-07-19 | Rapidol Ltd | Solvent dyeing of human hair |
| US3100739A (en) * | 1958-02-25 | 1963-08-13 | Therachemie Chem Therapeut | Process for dyeing human hair with water soluble, quaternary ammonium containing dyes |
| US3215605A (en) * | 1962-04-25 | 1965-11-02 | Revlon | Method for coloring hair and other keratinaceous fibers with metal salts |
| US3521989A (en) * | 1966-10-04 | 1970-07-28 | Commw Scient Ind Res Org | Method of dyeing wool and composition therefor |
| US4169706A (en) * | 1975-07-18 | 1979-10-02 | Ernst Kruchen | Method of cleaning poultry feathers |
| US6436380B1 (en) | 1992-12-31 | 2002-08-20 | Advantage Partners Llc | Baldness cosmetic and method of application |
| US6814957B1 (en) | 1992-12-31 | 2004-11-09 | Kenneth Pond | Baldness cosmetic and method of application |
| US5705030A (en) * | 1993-12-29 | 1998-01-06 | The United States Of America As Represented By The Secretary Of Agriculture | Fiber and fiber products produced from feathers |
| EP1454614A1 (en) * | 2003-03-06 | 2004-09-08 | KPSS-Kao Professional Salon Services GmbH | Composition for dyeing human hair |
| US20040231069A1 (en) * | 2003-03-06 | 2004-11-25 | Kpss-Kao Professional Salon Services Gmbh | Composition for dyeing human hair |
| US7135045B2 (en) | 2003-03-06 | 2006-11-14 | Kpss-Kao Professional Salon Services Gmbh | Composition for dyeing human hair |
| US20070006399A1 (en) * | 2003-03-06 | 2007-01-11 | Kpss-Kao Professional Salon Services Gmbh | Composition for Dyeing Human Hair |
| US7264639B2 (en) | 2003-03-06 | 2007-09-04 | Kpss-Kao Professional Salon Services Gmbh | Composition for dyeing human hair |
| AU2004200917B2 (en) * | 2003-03-06 | 2008-02-21 | Kpss-Kao Professional Salon Services Gmbh | Colouring composition for hair |
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