EP0780509A1 - Procédé amélioré de teinture ou d'impression de polyoléfines - Google Patents
Procédé amélioré de teinture ou d'impression de polyoléfines Download PDFInfo
- Publication number
- EP0780509A1 EP0780509A1 EP95203603A EP95203603A EP0780509A1 EP 0780509 A1 EP0780509 A1 EP 0780509A1 EP 95203603 A EP95203603 A EP 95203603A EP 95203603 A EP95203603 A EP 95203603A EP 0780509 A1 EP0780509 A1 EP 0780509A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dyeing
- carbon atoms
- polyolefin
- printing
- per weight
- 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- Withdrawn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
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 32
- 238000004043 dyeing Methods 0.000 title claims abstract description 24
- 238000000034 method Methods 0.000 title claims abstract description 19
- -1 dialkylaminoalkyl methacrylamide Chemical compound 0.000 claims abstract description 28
- 239000000835 fiber Substances 0.000 claims abstract description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000005977 Ethylene Substances 0.000 claims abstract description 8
- 229920001577 copolymer Polymers 0.000 claims abstract description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 238000002156 mixing Methods 0.000 claims abstract description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims abstract description 4
- 238000010014 continuous dyeing Methods 0.000 claims description 6
- 235000019864 coconut oil Nutrition 0.000 claims description 3
- 239000003240 coconut oil Substances 0.000 claims description 3
- 238000010016 exhaust dyeing Methods 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims description 3
- 239000012752 auxiliary agent Substances 0.000 claims 2
- 239000004743 Polypropylene Substances 0.000 description 13
- 229920001155 polypropylene Polymers 0.000 description 13
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 12
- 239000000975 dye Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 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 6
- 239000002253 acid Substances 0.000 description 6
- 239000000980 acid dye Substances 0.000 description 6
- 229920001038 ethylene copolymer Polymers 0.000 description 5
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 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 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- GVLHHJPRNMDLLL-UHFFFAOYSA-M sodium 7-amino-8-[[4-chloro-2-(trifluoromethyl)phenyl]diazenyl]-3-sulfonaphthalen-1-olate Chemical compound NC1=CC=C2C=C(C=C(O)C2=C1N=NC1=CC=C(Cl)C=C1C(F)(F)F)S(=O)(=O)O[Na] GVLHHJPRNMDLLL-UHFFFAOYSA-M 0.000 description 2
- 238000010025 steaming Methods 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- GDFCSMCGLZFNFY-UHFFFAOYSA-N Dimethylaminopropyl Methacrylamide Chemical compound CN(C)CCCNC(=O)C(C)=C GDFCSMCGLZFNFY-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000019233 fast yellow AB Nutrition 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
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000983 mordant dye Substances 0.000 description 1
- SHIJZXKPKFJRIS-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-2-methylprop-2-enamide;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.CCN(CC)CCNC(=O)C(C)=C SHIJZXKPKFJRIS-UHFFFAOYSA-N 0.000 description 1
- DCBBWYIVFRLKCD-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2-methylprop-2-enamide Chemical compound CN(C)CCNC(=O)C(C)=C DCBBWYIVFRLKCD-UHFFFAOYSA-N 0.000 description 1
- 150000002814 niacins Chemical class 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- NTOOJLUHUFUGQI-UHFFFAOYSA-M sodium;4-(4-acetamidoanilino)-1-amino-9,10-dioxoanthracene-2-sulfonate Chemical compound [Na+].C1=CC(NC(=O)C)=CC=C1NC1=CC(S([O-])(=O)=O)=C(N)C2=C1C(=O)C1=CC=CC=C1C2=O NTOOJLUHUFUGQI-UHFFFAOYSA-M 0.000 description 1
- KFLRWGSAMLBHBV-UHFFFAOYSA-M sodium;pyridine-3-carboxylate Chemical compound [Na+].[O-]C(=O)C1=CC=CN=C1 KFLRWGSAMLBHBV-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/46—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyolefins
-
- 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
- D06P1/613—Polyethers without nitrogen
- D06P1/6131—Addition products of hydroxyl groups-containing compounds with oxiranes
- D06P1/6133—Addition products of hydroxyl groups-containing compounds with oxiranes from araliphatic or aliphatic alcohols
-
- 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
- D06P1/613—Polyethers without nitrogen
- D06P1/6131—Addition products of hydroxyl groups-containing compounds with oxiranes
- D06P1/6135—Addition products of hydroxyl groups-containing compounds with oxiranes from aromatic alcohols or from phenols, naphthols
-
- 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
- D06P1/613—Polyethers without nitrogen
- D06P1/6136—Condensation products of esters, acids, oils, oxyacids with oxiranes
-
- 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
- D06P1/65131—Compounds containing ether or acetal 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
- D06P1/653—Nitrogen-free carboxylic acids or their salts
- D06P1/6533—Aliphatic, araliphatic or cycloaliphatic
-
- 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
- D06P3/79—Polyolefins
- D06P3/791—Polyolefins using acid dyes
Definitions
- This invention relates to an improved method for dyeing and printing of polyolefins. Especially the invention relates in improvements of fixation speed of acid dyes on acid dyeable polyolefins. Also, the invention relates to fibers and articles made of these fibres containing this dyeable polyolefin.
- Polyolefins such as polypropylene and polyethylene have excellent physical and mechanical properties and excellent processability.
- the dyeing of polyolefins, especially polypropylene, polyolefin fibers and articles made from the fibers with conventional acid dyes and dyeing technologies has been very difficult because of the hydrophobicity and the lack of sites where hydrogen bonds or electrostatic attraction can operate, it has been very difficult to dye fabricated articles of these polymers.
- crystalline polypropylene fibers are lightweight and strong and they have good heat-retaining properties. These fibers have been expected to have wide applications, but have still limited use because it has not been able to dye them by ordinary dyeing methods.
- a dyeable polyolefin which is obtained by blending 0,1 - 30 % by weight ethylene/aminoalkylacrylatecopolymer.
- ethylene/aminoalkylacrylatecopolymer Preferably it is a copolymer of ethylene and dimethylaminoethylmethacrylate.
- EP 269293 describes a method to incorporate dyesites in polyolefin matrix in order to obtain electrostatic attraction between acid dyestuffs and the polyolefin matrix.
- the corresponding copolymer is a copolymer of ethylene and dialkyl aminoalkylacrylamide.
- This the dyeable composition comprises 100 parts per weight polyolefin, 1-20 parts per weight the above mentioned copolymer and also 0-3 parts per weight at least one alkali metal salt of an organic carboxylic acid having 7-24 carbon atoms.
- modified polyolefins especially polypropylenes
- contain functional groups rendering it dyeable with acid dyes still the polypropylene matrix is very unpolar and therfor hydrophobic. A way to obtain deep enough colours with very long dyeing times is not attractive.
- Acid dyes are polar and water soluble and the dyeing happens from an aqueous solution.
- the combination of polar and unpolar phases is the subject of this invention.
- auxiliaries according to this invention are fatty alcohols or alkyl phenols of polyalkoxylated carboxylic acids of general formula (I): R - O -((CH 2 ) n - O) m - CH 2 - COOH (I) where
- Typical addition levels of the auxiliary (I) are 2-50 g/kg for printing paste, from 0.1-5 % on weight of fabric (owf) for exhaust dyeing and 1-50 g/litre for continuous dyeing applications, in particular with a liquid Pick Up (P.U.) of 100 %.
- the lower addition levels are for light shades, and the higher addition levels are for deep shades.
- This invention further concerns the fibers made from the dyeable polyolefin composition and the articles made from these fibers.
- the dyeable polyolefin composition according to this invention comprises a melt blended mixture of
- the polyolefin composition comprises
- the polyolefins (A) used in this invention are crystalline homopolymers of ⁇ -olefins like polyethylene, polypropylene, polybutene-1, poly-4-methylpentene-1 or various crystalline copolymers of those ⁇ -olefins. Most preferably the polyolefin is crystalline homopolymer or copolymer of propylene.
- the suitable melt index of polyolefins is 0.5 - 800.
- Suitable dialkylaminoalkyl methacrylamide or methacrylate comonomers for ethylene copolymers (B) are for example dimethylaminoethyl methacrylamide or methacryate, dimethylaminopropyl methacrylamide or methacrylate diethylaminoethyl methacrylamide or methacrylate.
- the alkyl groups are C 1 -C 4 alkyl groups, but most preferably the comonomer is dimethylaminopropyl methacrylamide.
- a suitable proportion of the comonomer unit in the ethylene copolymer is 5-60 % by weight, preferably 10-50 % by weight.
- the amount of ethylene copolymer (B) is 1-20 parts per weigth, based on 100 parts per weight polyolefin, preferably 2-10 parts per weight.
- the alkali metal salt of an organic carboxylic acid (C) is e.g. sodium, potassium or lithium salt of organic acids, such as higher fatty acids having 10-24 carbon atoms, aromatic acids or nicotinic acids.
- organic acids such as higher fatty acids having 10-24 carbon atoms, aromatic acids or nicotinic acids.
- Sodium or potassium stearate or benzoate, sodium p-tert-butylbenzoate or sodium nicotinate are preferred.
- the composition can be produced by conventional mixing methods, preferably by melt blending using an extruder or other suitable equipment.
- the dyeable polyolefin composition can be formed into fibers by conventional methods like melt spinning methods, but can also be fabricated into other forms such as films, sheets, tubes and into any extruded shape.
- the anionic dyes such as acid dyes, pre-metallised acid dyes, direct dyes or acid mordant dyes are dissolved in an exhaust dyeing bath, a continuous dyeing liquor, or a printing paste, which is adjusted to a suitable acidic condition by inorganic or organic acids such as acetic, oxalic, formic, citric, benzoic acid etc.
- the fibers or fiber products are then brought into contact with the dye solotion and heat treated at about 100 °C.
- This heat treatment especially when fiber products are dyed or printed, is very critical point in the process and should be made efficiently and with a high speed.
- the auxiliaries according to this invention make the high speed possible.
- the fixation time without the auxiliaries in the printing process is about 3 to 15 minutes, depending on depth of the shade. Light shades fix at 3 minutes, dark shades need 15 minutes for full dyestuff fixation. But according to this invention, the fixation time can be shortened to about 1.5 to 5 minutes depending on the depth of the shade.
- Polypropylene, melt index 18, (produced by Borealis N.V.) and 7 % by weight a copolymer of ethylene and dimethylaminopropyl methacrylamide (EDMAPMA) were melt blended and spun into filaments (1250/65 dtex) and tufted into a carpet.
- the carpets have been printed with a mixture of Colour Index (C.I.) Acid Yellow 216:1, C.I. Acid Red 266 and C.I. Acid Blue 40 to have a dark brown trichromatic colour.
- the printing paste contains a thickener such as a Guar Gum, the dyestuffs and citric acid to ensure the protonation of the acid dyesites in the modified polypropylene.
- the citric acid is added until pH value of 3.0-3.5 is obtained.
- Printing paste 1 contains the above mentioned elements (comparative)
- Printing paste 2 contains on top of above mentioned components 20 g/kg of fixation speed improvement auxiliary (I), where
- the carpets After printing, in order to fix the applied amount of dyestuff, the carpets go into a steamer for 2 minutes. Steaming conditions are 100 °C and relative humidity 50 %. After the fixation in the steamer, the carpets are rinsed in cold water and the colour depth of the fixed dyestuffs is evaluated visually or by means of spectrophotometer.
- the carpet printed with the paste 2 has the double colour depth of the carpet printed with paste 1.
- the same polypropylene composition as in example 1 was melt spun into fibers which were used to make hanks, which have been exhaust dyed with C.I Acid Red 266 to obtain a deep red colour.
- An exhaust dyebath is prepared with a solution of 2 % on weight of fabric (owf) of C.I. Acid Red 266 containing phormic acid to protonate the acid dyesites in the modified polypropylene.
- the pH is adjusted to 3.0-3.5.
- the hanks were put into the exhaust dyebath and heated up until 100 °C and stayed there until dyestuff exhaustion is obtained.
- the dyeing time for full exhaustion with dyebath 2 is 20 minutes and the dyeing time for exhaust dyebath 1 is 45 minutes.
- Example 2 Same dyeable polypropylene composition as in Example 1 was melt spun into multifilaments and tufted into a loop pile carpet.
- the carpets were continuos dyed by liquor application of the baths at P.U. of 250 %. After application, the colours were fixed by means of a steaming treatment (100 °C, 50 % relative humidity).
- the colour depth of the carpet dyed with bath 2 is double the colour depth of the carpet dyed with bath 1.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Coloring (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP95203603A EP0780509A1 (fr) | 1995-12-22 | 1995-12-22 | Procédé amélioré de teinture ou d'impression de polyoléfines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP95203603A EP0780509A1 (fr) | 1995-12-22 | 1995-12-22 | Procédé amélioré de teinture ou d'impression de polyoléfines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0780509A1 true EP0780509A1 (fr) | 1997-06-25 |
Family
ID=8220991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP95203603A Withdrawn EP0780509A1 (fr) | 1995-12-22 | 1995-12-22 | Procédé amélioré de teinture ou d'impression de polyoléfines |
Country Status (1)
| Country | Link |
|---|---|
| EP (1) | EP0780509A1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999044207A1 (fr) * | 1998-02-25 | 1999-09-02 | Abb Ab | Cable electrique de courant continu |
| EP2609170A1 (fr) | 2010-08-27 | 2013-07-03 | Board Of Regents, The University Of Texas System | Agents tensio-actifs alcoxy carboxylates |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3385652A (en) * | 1963-08-21 | 1968-05-28 | Union Carbide Corp | Dyeing polyolefin articles with soluble dye and a short chain polyethylene glycol ether |
| US3926553A (en) * | 1970-02-02 | 1975-12-16 | Uniroyal Inc | Method of rendering polyolefins dyeable with anionic dyes |
| EP0039207A1 (fr) * | 1980-04-25 | 1981-11-04 | Sumitomo Chemical Company, Limited | Procédé de teinture de matières fibreuses en polyoléfine |
| EP0269293A2 (fr) * | 1986-11-05 | 1988-06-01 | Sumitomo Chemical Company, Limited | Composition à base d'une poly-alpha-oléfine, apte à la teinture, et d'un copolymère |
-
1995
- 1995-12-22 EP EP95203603A patent/EP0780509A1/fr not_active Withdrawn
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3385652A (en) * | 1963-08-21 | 1968-05-28 | Union Carbide Corp | Dyeing polyolefin articles with soluble dye and a short chain polyethylene glycol ether |
| US3926553A (en) * | 1970-02-02 | 1975-12-16 | Uniroyal Inc | Method of rendering polyolefins dyeable with anionic dyes |
| EP0039207A1 (fr) * | 1980-04-25 | 1981-11-04 | Sumitomo Chemical Company, Limited | Procédé de teinture de matières fibreuses en polyoléfine |
| EP0269293A2 (fr) * | 1986-11-05 | 1988-06-01 | Sumitomo Chemical Company, Limited | Composition à base d'une poly-alpha-oléfine, apte à la teinture, et d'un copolymère |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999044207A1 (fr) * | 1998-02-25 | 1999-09-02 | Abb Ab | Cable electrique de courant continu |
| EP2609170A1 (fr) | 2010-08-27 | 2013-07-03 | Board Of Regents, The University Of Texas System | Agents tensio-actifs alcoxy carboxylates |
| US8822391B2 (en) | 2010-08-27 | 2014-09-02 | Board Of Regents, The University Of Texas System | Alkoxy carboxylate surfactants |
| US9783729B2 (en) | 2010-08-27 | 2017-10-10 | Board Of Regents, The University Of Texas Systems | Alkoxy carboxylate surfactants |
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