EP0036252B1 - Verfahren zum Bedrucken von Textilien - Google Patents
Verfahren zum Bedrucken von Textilien Download PDFInfo
- Publication number
- EP0036252B1 EP0036252B1 EP19810300721 EP81300721A EP0036252B1 EP 0036252 B1 EP0036252 B1 EP 0036252B1 EP 19810300721 EP19810300721 EP 19810300721 EP 81300721 A EP81300721 A EP 81300721A EP 0036252 B1 EP0036252 B1 EP 0036252B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- disperse
- dyestuffs
- dyestuff
- alkali
- carboxylic 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.)
- Expired
Links
- 238000000034 method Methods 0.000 title claims description 27
- 230000008569 process Effects 0.000 title claims description 22
- 239000004753 textile Substances 0.000 title claims description 21
- 238000007639 printing Methods 0.000 title claims description 17
- 239000000975 dye Substances 0.000 claims description 52
- 239000000463 material Substances 0.000 claims description 35
- 239000004115 Sodium Silicate Substances 0.000 claims description 20
- 239000003513 alkali Substances 0.000 claims description 20
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 20
- 239000004111 Potassium silicate Substances 0.000 claims description 14
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 claims description 14
- 229910052913 potassium silicate Inorganic materials 0.000 claims description 14
- 235000019353 potassium silicate Nutrition 0.000 claims description 14
- 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 claims description 12
- 238000010168 coupling process Methods 0.000 claims description 12
- 238000005859 coupling reaction Methods 0.000 claims description 12
- VGKYEIFFSOPYEW-UHFFFAOYSA-N 2-methyl-4-[(4-phenyldiazenylphenyl)diazenyl]phenol Chemical compound Cc1cc(ccc1O)N=Nc1ccc(cc1)N=Nc1ccccc1 VGKYEIFFSOPYEW-UHFFFAOYSA-N 0.000 claims description 10
- 230000000694 effects Effects 0.000 claims description 10
- 229920002994 synthetic fiber Polymers 0.000 claims description 9
- 239000004758 synthetic textile Substances 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 8
- JSFUMBWFPQSADC-UHFFFAOYSA-N Disperse Blue 1 Chemical compound O=C1C2=C(N)C=CC(N)=C2C(=O)C2=C1C(N)=CC=C2N JSFUMBWFPQSADC-UHFFFAOYSA-N 0.000 claims description 7
- TUXJTJITXCHUEL-UHFFFAOYSA-N disperse red 11 Chemical compound C1=CC=C2C(=O)C3=C(N)C(OC)=CC(N)=C3C(=O)C2=C1 TUXJTJITXCHUEL-UHFFFAOYSA-N 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
- 229910052681 coesite Inorganic materials 0.000 claims description 6
- 230000008878 coupling Effects 0.000 claims description 6
- 229910052906 cristobalite Inorganic materials 0.000 claims description 6
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 6
- 238000010018 discharge printing Methods 0.000 claims description 6
- 229910052682 stishovite Inorganic materials 0.000 claims description 6
- 229910052905 tridymite Inorganic materials 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- -1 alkali metal salt Chemical class 0.000 claims description 5
- 238000010025 steaming Methods 0.000 claims description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims description 5
- 239000002562 thickening agent Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims description 4
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 4
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 4
- 238000010019 resist printing Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- ZLCUIOWQYBYEBG-UHFFFAOYSA-N 1-Amino-2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=C(N)C(C)=CC=C3C(=O)C2=C1 ZLCUIOWQYBYEBG-UHFFFAOYSA-N 0.000 claims description 3
- 125000000686 lactone group Chemical group 0.000 claims description 3
- MIHADVKEHAFNPG-UHFFFAOYSA-N 2-Amino-5-nitrothiazole Chemical compound NC1=NC=C([N+]([O-])=O)S1 MIHADVKEHAFNPG-UHFFFAOYSA-N 0.000 claims description 2
- KVQZMLBWGHLHTR-UHFFFAOYSA-N 2-[4-(2,2-dicyanoethenyl)-n-ethyl-3-methylanilino]ethyl n-phenylcarbamate Chemical compound C=1C=C(C=C(C#N)C#N)C(C)=CC=1N(CC)CCOC(=O)NC1=CC=CC=C1 KVQZMLBWGHLHTR-UHFFFAOYSA-N 0.000 claims description 2
- 229940018167 2-amino-5-nitrothiazole Drugs 0.000 claims description 2
- ALLWOAVDORUJLA-UHFFFAOYSA-N Rebamipida Chemical compound C=1C(=O)NC2=CC=CC=C2C=1CC(C(=O)O)NC(=O)C1=CC=C(Cl)C=C1 ALLWOAVDORUJLA-UHFFFAOYSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 150000001448 anilines Chemical class 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- 239000003906 humectant Substances 0.000 claims description 2
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- GLQWRXYOTXRDNH-UHFFFAOYSA-N thiophen-2-amine Chemical class NC1=CC=CS1 GLQWRXYOTXRDNH-UHFFFAOYSA-N 0.000 claims description 2
- 150000003577 thiophenes Chemical class 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 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 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000000986 disperse dye Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- RQLMZSLFKGNXTO-UHFFFAOYSA-N 1-amino-4-hydroxy-2-(6-hydroxyhexoxy)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC(OCCCCCCO)=C2N RQLMZSLFKGNXTO-UHFFFAOYSA-N 0.000 description 1
- BBFRYSKTTHYWQZ-UHFFFAOYSA-N 4-anilino-3-nitro-n-phenylbenzenesulfonamide Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)NC=2C=CC=CC=2)=CC=C1NC1=CC=CC=C1 BBFRYSKTTHYWQZ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- RQILFETZQXVWKX-UHFFFAOYSA-N ac1l570z Chemical compound C1=CC=C2N(C(C3=CC=C4C(=O)N(C(C=5C(C#N)=CC6=C3C4=5)=O)CCCOC)=O)C6=NC2=C1 RQILFETZQXVWKX-UHFFFAOYSA-N 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N aconitic acid Chemical compound OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 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 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001733 carboxylic acid esters Chemical group 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- FFYADPKAFBYAMU-UHFFFAOYSA-N ethane-1,2-diol;urea Chemical compound NC(N)=O.OCCO FFYADPKAFBYAMU-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- LVWZTYCIRDMTEY-UHFFFAOYSA-N metamizole Chemical compound O=C1C(N(CS(O)(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 LVWZTYCIRDMTEY-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical group [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 239000007762 w/o emulsion 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
- D06P3/34—Material containing ester groups
- D06P3/52—Polyesters
- D06P3/54—Polyesters using dispersed dyestuffs
-
- 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
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/15—Locally discharging the dyes
- D06P5/151—Locally discharging the dyes with acids or bases
Definitions
- This invention relates to an improved process for the resist or discharge printing of synthetic textile materials.
- Resist printing is a method of textile printing in which an undyed textile material is first printed with a substance (the resist) which prevents the uptake or fixation of a subsequently applied dyestuff, so that there is obtained a white pattern on a coloured ground, or a pattern of contrasting colour to the ground by incorporating suitable dyestuffs or colour-producing substances in the resist print paste.
- a substance the resist
- Discharge printing is a method of textile printing in which dyed textile material is printed with a chemical composition (the discharge) that destroys the dyestuff locally to give a white pattern, or in which a second dyestuff, applied simultaneously with the discharge, produces a pattern of contrasting colour.
- GB-A-1543724 describes and claims a process for producing discharge printing effects in a coloured ground shade on a synthetic textile material, which comprises applying to that area of the material where the ground shade and the discharge effect are wanted one or more disperse dyes which contain at least one carboxylic ester group but are free from carboxylic acid and sulphonic acid groups, and in a separate stage applying to the material where the discharge effect is wanted a printing paste which is alkaline or becomes alkaline on heating or steaming and which does not contain any reducing agent, thereafter heating or steaming the material and thereafter washing the material.
- stages 1 and 3 can be reversed, so that the dyestuff is applied to the textile material before the alkaline print paste.
- stage 5 in which the textile material is subjected to the action of heat or steam, the disperse dyestuff in contact with the alkali is converted into a water-soluble form, whilst the disperse dyestuff which is not in contact with the alkali is fixed on the textile material.
- the water-soluble form of the dyestuff is then removed from the textile material by the washing treatment of stage 6.
- stage 2 it would be desirable if, in the above process, the first drying operation (stage 2) could be eliminated so that stage 1 is followed immediately by stage 3.
- This "wet-on-wet" process would have the advantages that the process has one stage less, with consequent saving in drying plant occupation time, and also the saving in the energy used to effect drying.
- GB-A-1481741 describes the production of multicolour effects using alkali sensitive disperse dyes of a different type to GB-A-1543724 applied in conjunction with alkaline agents.
- wet-on-wet resist or discharge prints having sharp definition between the different coloured areas of the print can be obtained if the alkali used in the print paste is sodium or potassium silicate and if specific types of alkali dischargeable dyestuffs are applied.
- a process for producing resist or discharge printing effects on a synthetic textile material which comprises applying to the textile material, in either order (i) an alkaline printing paste which may contain one or more disperse dyestuffs free from sulphonic acid, carboxylic acid and carboxylic acid ester groups, the said dyestuffs being unaffected by alkali at the concentration present, and (ii) a printing paste or passing liquor containing at least one alkali dischargeable disperse dyestuff free from sulphonic acid and carboxylic acid groups, and free from carboxylic acid ester groups which if hydrolysed would leave free carboxylic acid groups attached to the dyestuff molecule, thereafter heating or steaming the material and thereafter washing the material characterised by the presence of sodium or potassium silicate in (i), a carboxylic acid in (ii), and without drying between the application of (i) and (ii).
- alkali-dischargeable dyestuffs which are used in the process according to the present invention may be broadly classified as follows:
- miscellaneous dyestuffs C.I. Disperse Violet 88, C.I. Disperse Yellow 180, C.I. Disperse Violet 48, C.I. Disperse Blue 92, C.I. Disperse Yellow 93, C.I. Disperse Yellow 201, C.I. Disperse Yellow 88, C.I. Disperse Yellow 210, C.I. Disperse Red 203 and C.I. Disperse Yellow 202.
- dyestuffs which may be used in the present process are those which discharge only partially (i.e. do not give a white discharge) and which do not leave a weak enough stain to allow all shades of illumination to be used, but which do show an even residual shade that allows the use of such dyestuffs for limited illuminated shades and which may be used for shading purposes.
- miscellaneous dyestuffs of formulae Red which is disclosed in GB-A-859899, and Red which is disclosed in GB-A-1027968, together with C.I. Disperse Red 72, C.I. Disperse Blue 139, C.I. Disperse Orange 55, C.I. Disperse Red 329 and C.I. Disperse Violet 40.
- Any disperse dyestuff which undergoes chromophore destruction in the presence of alkali to an extent such as to make it suitable for a ground shade in discharge printing may be used in the present process, provided that it is free from -COOH, -S0 3 H and -COOR- groups as defined in claim 1.
- the sodium silicate which is used in the above process may be any of those grades of sodium silicate which are commercially available and is preferably a sodium silicate in which the molecular ratio of SiO 2 to Na 2 0 is from 1.65:1.0 to 4.0:1.0.
- the potassium silicate which is used preferably has a molecular ratio of Si0 2 to K 2 0 of from 2.0:1 to 4.0:1.
- the amount of sodium or potassium silicate which is used in the printing paste (I) must provide sufficient alkali to discharge the disperse dyestuff in the padding liquor or printing paste (ii), and may be from 50 to 300 parts by weight per 1000 parts by weight of printing paste.
- a sodium or potassium silicate having a high molecular ratio of SiO 2 to Na 2 0 or K 2 0 can be replaced in the printing paste by a smaller quantity of sodium or potassium silicate having a lower molecular ratio of Si0 2 to Na 2 0 or K 2 0, without affecting the result.
- the printing paste containing the sodium or potassium silicate may also contain a humectant such as ethylene glycol urea or, preferably, glycerol, a dye solvent such as polyethylene glycol, for example, a polyethylene glycol having a molecular weight in the region of 300, and a thickening agent.
- a humectant such as ethylene glycol urea or, preferably, glycerol
- a dye solvent such as polyethylene glycol, for example, a polyethylene glycol having a molecular weight in the region of 300
- a thickening agent e.glycerol
- suitable thickeners are starch derivatives such as starch ethers, carob-seed gum ethers, modified carboxymethylcelluloses and combinations of these, optionally in admixture with water-in-oil or oil-in-water emulsion.
- the padding liquor or print paste used to apply the alkali-dischargeable disperse dyestuff will also contain a carboxylic acid, for example, citric acid, to prevent premature interaction of the dyestuff with the alkaline sodium or potassium silicate, and may contain a thickener such as one of those thickeners already mentioned above.
- a carboxylic acid for example, citric acid
- a thickener such as one of those thickeners already mentioned above.
- adjuvants which are conventionally employed in the application of disperse dyestuffs to synthetic textile materials from such media, for example carriers, fixation assistants, level dyeing assistants, dispersing agents and antifoam agents.
- the heat treatment to which the textile material is subjected after the application of the print paste containing the sodium or potassium silicate and the print paste or padding liquor containing the disperse dyestuff can comprise a heat treatment for a short period at temperatures from 150° to 220°C. It is, however, preferred to subject the textile material to a steaming treatment, for example, saturated steam at 100°C for a few minutes followed by a dry heat treatment at 160° to 220°C or superheated steam at 150° to 200°C, or the use of saturated steam under pressure at 115° to 150°C.
- the synthetic textile material used in the process of the invention can be in the form of nonwoven fabric, felt, woven or knitted goods, or carpets.
- synthetic textile materials there may be mentioned secondary cellulose acetate and cellulose triacetate, polypropylene, acrylic, polyamide, and preferably aromatic polyester textile material.
- the alkali-dischargeable disperse dyestuff can be used together with a reactive dye whose reactive groups, such as sulphato- ethylsulphone groups, form a dye-fibre bond with the hydroxyl groups of the cellulose textile material which is hydrolysed under the alkaline conditions in those areas where the alkaline print paste is applied, or a reactive dyestuff containing one or more phosphonic acid groups which does not fix on cellulose in the presence of alkali.
- a reactive dye whose reactive groups, such as sulphato- ethylsulphone groups, form a dye-fibre bond with the hydroxyl groups of the cellulose textile material which is hydrolysed under the alkaline conditions in those areas where the alkaline print paste is applied, or a reactive dyestuff containing one or more phosphonic acid groups which does not fix on cellulose in the presence of alkali.
- the disperse. dyestuff or dyestuffs which are optionally used in the alkaline printing paste containing sodium or potassium silicate can be any of the disperse dyestuffs free from -S0 3 H, --COOH and ⁇ COOR groups (as defined in claim 1) and not adversely affected by alkali which are conventionally employed in colouring synthetic textile materials. Examples of such dyestuffs are given in, for example, the Third Edition of the Colour Index which was published in 1971.
- a resist print paste comprising: is printed on to a woven polyethylene terephthalate textile material, and without drying the textile material is then coated over all, including that part which has already been printed with the above resist paste, with the following print paste comprising:
- the textile material is then dried on drying cylinders for 2 minutes at approximately 95°C, high temperature steamed at 170°C, for 8 minutes, washed off using the six-stage washing sequence described above and finally dried.
- the resulting blue on white pattern has excellent definition.
- sodium silicate used in the above example is replaced by the same amount of a sodium silicate in which the molecular ratio of Si0 2 to Na 2 0 is 1.65:1.0 a similar result is obtained; the amount of this latter sodium silicate can also be reduced to 100 parts without adverse effect on the sharpness of the resulting print.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Coloring (AREA)
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT81300721T ATE11310T1 (de) | 1980-03-13 | 1981-02-20 | Verfahren zum bedrucken von textilien. |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8008597 | 1980-03-13 | ||
GB8008597 | 1980-03-13 | ||
GB8014139 | 1980-04-29 | ||
GB8014139 | 1980-04-29 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0036252A2 EP0036252A2 (de) | 1981-09-23 |
EP0036252A3 EP0036252A3 (en) | 1981-11-18 |
EP0036252B1 true EP0036252B1 (de) | 1985-01-16 |
Family
ID=26274812
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19810300721 Expired EP0036252B1 (de) | 1980-03-13 | 1981-02-20 | Verfahren zum Bedrucken von Textilien |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0036252B1 (de) |
DE (1) | DE3168222D1 (de) |
ES (1) | ES8207251A1 (de) |
PT (1) | PT72662B (de) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3041014A1 (de) * | 1980-10-31 | 1982-06-16 | Cassella Ag, 6000 Frankfurt | Verfahren zur herstellung von aetzreservedrucken von textilmaterialien |
DE3312488A1 (de) * | 1983-04-07 | 1984-10-11 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung alkalisch aetzbarer faerbungen und drucke |
US4559781A (en) * | 1983-10-31 | 1985-12-24 | Allied Corporation | Master cylinder |
JPS6219105A (ja) * | 1985-07-18 | 1987-01-27 | ワイケイケイ株式会社 | 図柄、文字入り面フアスナ−の製造方法 |
DE3718565A1 (de) * | 1987-06-03 | 1988-12-15 | Basf Ag | Verfahren zur herstellung von aetzdrucken |
GB8920004D0 (en) | 1989-09-05 | 1989-10-18 | John Green & Son Plc | Printing of fabrics |
ITSA20120006A1 (it) * | 2012-05-10 | 2013-11-11 | Oz Anadolu Kimya Sanayi Ve Ticaret Anonim Sirketi | Innovazione nelle paste corrodenti per la stampa tessile. |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2322323A (en) * | 1941-04-16 | 1943-06-22 | Celanese Corp | Discharge printing of textiles |
ZA745027B (en) * | 1973-08-16 | 1975-08-27 | Hoechst Ag | Process for obtaining irregular shadow dyeings on polyester fibres and mixtures thereof |
ZA744836B (en) * | 1973-08-16 | 1975-08-27 | Hoechst Ag | Process for obtaining multicolor effects |
GB1543724A (en) * | 1975-08-13 | 1979-04-04 | Ici Ltd | Process for the production of discharge printing effects on synthetic textile materials |
GB1512321A (en) * | 1976-01-05 | 1978-06-01 | Ici Ltd | Colouration process for cellulose textile materials |
DE2836391C2 (de) * | 1978-08-19 | 1988-04-14 | Cassella Ag, 6000 Frankfurt | Verfahren zum Färben und Bedrucken von synthetischem hydrophobem Fasermaterial |
DE3064390D1 (en) * | 1979-07-18 | 1983-09-01 | Ici Plc | Substituted 2,7-dioxo-2,7-dihydrobenzo(1:2-b; 5,6-b1)difuran or dipyrrole dyestuffs, processes for their preparation and their use for the colouration of aromatic polyester textile materials |
-
1981
- 1981-02-20 EP EP19810300721 patent/EP0036252B1/de not_active Expired
- 1981-02-20 DE DE8181300721T patent/DE3168222D1/de not_active Expired
- 1981-03-12 ES ES500294A patent/ES8207251A1/es not_active Expired
- 1981-03-13 PT PT7266281A patent/PT72662B/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE3168222D1 (en) | 1985-02-28 |
EP0036252A2 (de) | 1981-09-23 |
ES500294A0 (es) | 1982-09-01 |
EP0036252A3 (en) | 1981-11-18 |
PT72662A (en) | 1981-04-01 |
ES8207251A1 (es) | 1982-09-01 |
PT72662B (en) | 1982-03-19 |
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