EP0023660B1 - Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques - Google Patents
Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques Download PDFInfo
- Publication number
- EP0023660B1 EP0023660B1 EP80104279A EP80104279A EP0023660B1 EP 0023660 B1 EP0023660 B1 EP 0023660B1 EP 80104279 A EP80104279 A EP 80104279A EP 80104279 A EP80104279 A EP 80104279A EP 0023660 B1 EP0023660 B1 EP 0023660B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dyestuff
- alkali
- dye
- reactive
- printing paste
- 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
- 239000000203 mixture Substances 0.000 title claims description 28
- 238000000034 method Methods 0.000 title claims description 22
- 230000000694 effects Effects 0.000 title claims description 11
- 229920000728 polyester Polymers 0.000 title claims description 8
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000000975 dye Substances 0.000 claims description 39
- 239000000835 fiber Substances 0.000 claims description 22
- 239000003513 alkali Substances 0.000 claims description 19
- 230000002378 acidificating effect Effects 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 12
- 229920006395 saturated elastomer Polymers 0.000 claims description 11
- 239000003638 chemical reducing agent Substances 0.000 claims description 9
- 230000007935 neutral effect Effects 0.000 claims description 9
- 238000010025 steaming Methods 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- 125000000129 anionic group Chemical group 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 238000004040 coloring Methods 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 238000005470 impregnation Methods 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 238000010019 resist printing Methods 0.000 claims 6
- 239000000986 disperse dye Substances 0.000 description 29
- 238000007639 printing Methods 0.000 description 27
- 239000000985 reactive dye Substances 0.000 description 27
- 239000004744 fabric Substances 0.000 description 18
- 239000000984 vat dye Substances 0.000 description 16
- 238000001035 drying Methods 0.000 description 13
- 239000000976 ink Substances 0.000 description 12
- 229920003043 Cellulose fiber Polymers 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 238000005530 etching Methods 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- 239000002202 Polyethylene glycol Substances 0.000 description 8
- 239000012669 liquid formulation Substances 0.000 description 8
- 229920001223 polyethylene glycol Polymers 0.000 description 8
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 8
- -1 alkaline earth metal salts Chemical class 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000002657 fibrous material Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000004627 regenerated cellulose Substances 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229920000161 Locust bean gum Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000711 locust bean gum Substances 0.000 description 3
- 235000010420 locust bean gum Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 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 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- CXHHBNMLPJOKQD-UHFFFAOYSA-N methyl hydrogen carbonate Chemical compound COC(O)=O CXHHBNMLPJOKQD-UHFFFAOYSA-N 0.000 description 2
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 2
- 235000019799 monosodium phosphate Nutrition 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 238000010405 reoxidation reaction Methods 0.000 description 2
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical group COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- AKQMZZOTFNLAQJ-UHFFFAOYSA-N 1,1,2,2-tetrafluorocyclobutane Chemical compound FC1(F)CCC1(F)F AKQMZZOTFNLAQJ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- IHDBZCJYSHDCKF-UHFFFAOYSA-N 4,6-dichlorotriazine Chemical group ClC1=CC(Cl)=NN=N1 IHDBZCJYSHDCKF-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
- ORLGPUVJERIKLW-UHFFFAOYSA-N 5-chlorotriazine Chemical group ClC1=CN=NN=C1 ORLGPUVJERIKLW-UHFFFAOYSA-N 0.000 description 1
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- RDXLYGJSWZYTFJ-UHFFFAOYSA-N Niridazole Chemical compound S1C([N+](=O)[O-])=CN=C1N1C(=O)NCC1 RDXLYGJSWZYTFJ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical class 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical class 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- POJOORKDYOPQLS-UHFFFAOYSA-L barium(2+) 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonate Chemical compound [Ba+2].C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O.C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O POJOORKDYOPQLS-UHFFFAOYSA-L 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000010017 direct printing Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical group C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- SBGKURINHGJRFN-UHFFFAOYSA-N hydroxymethanesulfinic acid Chemical compound OCS(O)=O SBGKURINHGJRFN-UHFFFAOYSA-N 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229960005130 niridazole Drugs 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
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical class C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000001017 thiazole dye Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- 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
-
- 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
Definitions
- EP-A1-21 432 (not pre-published) is in turn concerned with conversion and etching reserve articles which are obtained when a reactive dye or a mixture of reactive and vat dyes is printed on cellulose fabric as a base in the weakly acidic medium and then a specially activated one Reducing agent from neutral medium and possibly the vat dye is overprinted, whereupon the simultaneous fixation of both dye classes takes place according to a two-phase process.
- the object of the present invention was therefore to produce white and colored reserves on mixed materials made of polyester and cellulose fibers.
- This object is achieved according to the invention by applying a slightly acidic preparation to the mixed material, the at least one etchable reactive dye which stains both types of fibers, or a mixture of at least one etchable reactive dye and at least one disperse dye which is mixed with alkali in a water-soluble anionic Form can be transferred, and possibly contains a neutral fixing aid for reactive dyes, then an alkaline etching reserve printing paste is printed on this rear impregnation, which contains a reducing agent and possibly a non-etchable dye in addition to the alkali, followed by fixing with superheated steam or saturated steam in conjunction with hot air takes place, and if the acidic preparation does not contain the neutral fixing aid, treatment with alkaline agents and a steaming process follow.
- White reserves are obtained by this process.
- vat dyes, alkali-stable or viable disperse dyes or a combination of such dyes are added to the alkaline printing paste.
- conversion articles can also be produced if non-etchable dyes are added to the acidic preparation.
- the colored substrates according to the invention comprise mixed materials made of polyester fibers, in particular polyethylene glycol terephthalate fibers, and natural and regenerated cellulose fibers in all usual mixing ratios.
- the weakly acidic preparation is advisable by padding or splashing, however also applied by printing, especially when large-area patterns (decks) are pre-printed.
- the embodiment of the process according to the invention in which the acidic preparation contains one or more etchable reactive dyes which stain both types of fibers, has the advantage that there are no fission products of disperse dyes which can be difficult to remove from the cellulose fiber. These dyes are preferably applied together with the neutral fixing aid for reactive dyes, whereupon they are fixed in a superheated steam atmosphere.
- Disperse dyes which can be converted into a water-soluble anionic form with alkali, in particular at a higher temperature, are known.
- the alkali solubility of these dyes is dependent on functional groups, especially esterified carboxy groups or phenolic or enolic hydroxyl groups or a combination of such groups.
- these disperse dyes no longer attach to the polyester fiber and can also be easily removed from the cellulose fiber.
- the neutral fixing aid for reactive dyes causes the reactive dye to be fixed on the fund in the course of the steaming operation with superheated steam.
- these auxiliaries are alkali metal or alkaline earth metal salts of aliphatic or aromatic, preferably low molecular weight, mono- or polycarboxylic acids, in particular alkali metal or alkaline earth metal salts of multiply halogenated low molecular weight aliphatic carboxylic acids and low molecular weight cyclic carbonic acid esters.
- the alkaline etching can p aste be printed without intermediate drying. In general, however, intermediate drying is recommended.
- the etching paste contains alkali, preferably in the form of alkali hydroxide or carbonate or a mixture of both, and a reducing agent which is customary in etching and vat printing inks, preferably a stabilized sulfinate, in particular the sodium salt of hydroxymethanesulfinic acid.
- a suitable dye or a mixture of dyes is added to the alkaline etching paste, which is selected from the range of vat dyes, the alkali-stable dispersion dyes and the combinable dispersion dyes. Combinations of several dyes from different classes are also possible.
- the alkaline printing paste contains a vat dye
- treatment with saturated steam at atmospheric pressure follows.
- the vat dye is incubated so that it can be drawn onto the cellulose portion of the mixed fiber material.
- vat dyes are very sensitive to temperatures above 100 ° C during the fixing process, but high-temperature fixing is required for the dyes on the polyester fiber portion, it is advisable to add an auxiliary agent that releases water above 100 ° C. This prevents or otherwise at least strongly suppresses the clouding of the color tone.
- auxiliary agent that releases water above 100 ° C. This prevents or otherwise at least strongly suppresses the clouding of the color tone.
- auxiliary agents of this type are aqueous dispersions of polymers, for example ethylene polymers, but especially organic dicarboxylic acids which are expediently used in the form of their salts, for example their alkali metal salts. From these aids, 50 to 400 g per kilogram of printing paste are appropriately added.
- colored reserves are generated with the aid of alkali-stable disperse dyes which are added to the alkaline etching paste.
- This alkali-stable disperse dye is advantageously used in combination with a vat dye which has the same shade.
- colored reserve effects are generated with the aid of combinable disperse dyes, which penetrate into the cellulose fiber in a coupled form, where they are firmly anchored in the course of the reoxidation.
- the fixation of the coloring depends on the dyes used. As mentioned, a saturated steam treatment is required when using vat dyes, which can be omitted if, apart from the reactive dyes, only disperse dyes are used. If saturated steam treatment is carried out, the destruction of the reactive dye by the reducing agent and the conversion of the alkali-sensitive disperse dye into its water-soluble anionic form take place in this step.
- the disperse dyes are expediently fixed in the same unit as a previous saturated steam treatment with superheated steam or hot air in connection with saturated steam. This also promotes reoxidation of the vat dye. If the acidic preparation contains the neutral fixing aid for reactive dyes, the reactive dye is also fixed in this step.
- the reactive dye is steamed after the fixation of the other dyes process fixed.
- alkali is applied to the fiber material, preferably in the form of alkali hydroxide, carbonate, bicarbonate, phosphate or silicate or a mixture of such alkalis. It can be applied in any manner, for example by spraying, padding or splashing.
- the subsequent steaming process is advantageously carried out as short-term steaming in saturated steam, which requires 2 to 20 seconds.
- the reactive dyes which can be used in the process according to the invention can belong to the various organic dye classes, for example azo, anthraquinone and phthalocyanine dyes, which contain at least one P-hydroxyethylsulfonic sulfuric acid ester group, vinylsulfonyl group, monochlorotriazine group, dichlorotriazine group, 2,2,3,3-tetrafluorocyclobutane contain acroylamlnooeuvre, vinylsulfonylamino group, ß-Hydroxyäthylsulfonylaminosulfuric acid ester group, P-phenylsulfonylpropionylamino group or a dichloroquinoxaline radical.
- organic dye classes for example azo, anthraquinone and phthalocyanine dyes, which contain at least one P-hydroxyethylsulfonic sulfuric acid ester group, vinylsulfonyl group, monochlor
- the disperse dyes that can be converted into a water-soluble anionic form with alkali, preferred are those whose cleavage products are easy to eliminate. Dyes which contain one or more carboxylic acid ester groups and nitro-thiazole dyes are preferred.
- Disperse dyes with anthraquinone structure which can be linked, and naphthalene di- and tetracarboxylic acid derivatives and quinophthalone derivatives, which are resistant to alkali and reducing agents, are suitable for the colored etching reserve effects.
- Vat dyes are in particular indigoide, thioindigoide, anthraquinone or naphthochinoid compounds, which are advantageously used in the commercially available dough form.
- locust bean gum ether thickeners come into consideration. Of this, 50 to 200 g of a 4 to 8% strength aqueous preparation are expediently added per liter of liquor.
- Suitable thickeners for the printing pastes are, for example, mixtures of degraded types of rubber and low-viscosity alginates or locust bean gum carboxymethyl ether and starch carboxymethyl ether.
- the goods are treated with superheated steam for 8 minutes at 180 ° C, briefly rinsed, reoxidized at 50 ° C with 2 g / I hydrogen peroxide and 5 ml / I acetic acid, rinsed again and finally with 0.5 g / I of a 20-fold oxyethylated nonylphenol washed at 90 ° C, rinsed and dried.
- a brilliant red print is obtained on a greenish-yellow background with good fastness properties.
- the goods After printing and drying, the goods are steamed for 10 minutes at 102 ° C in saturated steam and then for 7 minutes at 175 ° C in superheated steam.
- the further treatment is carried out as in Example 1.
- the knitted fabric is printed with an ink of the same composition as in Example 1, but with
- the fabric After printing and drying, the fabric is padded with 50 g / l acetic acid in a block bath with a squeezing effect of 70% and then steamed for 8 minutes at 175 ° C in superheated steam.
- the result is a deep blue print on a red background with good fastness properties.
- the fabric After drying, the fabric is printed with a printing ink which, apart from the dye, contains the same constituents as described in Example 1.
- the printed and dried goods are steamed for 7 minutes at 180 ° C in superheated steam, with a squeezing effect of 70% padded with a liquor of 100 g / l 32.5% sodium hydroxide solution and 150 g / l sodium carbonate and 8 seconds in saturated steam Steamed 102 ° C.
- Completion is as in example 1.
- the printed and dried fabric is passed through superheated steam at 180 ° C. for 7 minutes and then further treated as in Example 1.
- the fabric is printed with a printing ink which is composed according to Example 1, but contains no glycerol and 150 g sodium formaldehyde sulfoxylate and correspondingly 160 g water or thickener.
- a printing ink which is composed according to Example 1, but contains no glycerol and 150 g sodium formaldehyde sulfoxylate and correspondingly 160 g water or thickener.
- the goods are treated with superheated steam at 180 ° C. for 8 minutes, briefly rinsed, reoxidized as usual, washed with 0.5 g / l of a 20-fold ethylated nonylphenol at 90 ° C., rinsed and dried.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Claims (8)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2930541 | 1979-07-27 | ||
| DE19792930541 DE2930541A1 (de) | 1979-07-27 | 1979-07-27 | Verfahren zur herstellung von reserveeffekten auf mischmaterialien aus polyester- und cellulosefasern |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP0023660A2 EP0023660A2 (fr) | 1981-02-11 |
| EP0023660A3 EP0023660A3 (en) | 1981-05-06 |
| EP0023660B1 true EP0023660B1 (fr) | 1983-09-28 |
Family
ID=6076962
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP80104279A Expired EP0023660B1 (fr) | 1979-07-27 | 1980-07-21 | Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP0023660B1 (fr) |
| DE (2) | DE2930541A1 (fr) |
Families Citing this family (4)
| 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 |
| DE3439532A1 (de) * | 1984-10-29 | 1986-04-30 | Hoechst Ag, 6230 Frankfurt | Verfahren zum erzeugen von weiss- und buntreserven auf polyamidfasermaterialien |
| DE4446943A1 (de) * | 1994-12-28 | 1996-07-04 | Cassella Ag | Verfahren zum Färben von Polyester und polyesterhaltigen Textilmaterialien |
| CN103451800B (zh) * | 2013-09-03 | 2016-02-03 | 无锡市天然绿色纤维科技有限公司 | 一种色纺纱线及其加工方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1929231B2 (de) * | 1969-06-10 | 1973-08-23 | Farbwerke Hoechst AG, vormals Mei ster Lucius & Bruning, 6000 Frankfurt | Verfahren zur herstellung rapportlos gemusterter druckartikel auf textilen flaechengebilden aus nativen oder regenerierten cellulosefasern |
| GB1543724A (en) * | 1975-08-13 | 1979-04-04 | Ici Ltd | Process for the production of discharge printing effects on synthetic textile materials |
| DE2836391C2 (de) * | 1978-08-19 | 1988-04-14 | Cassella Ag, 6000 Frankfurt | Verfahren zum Färben und Bedrucken von synthetischem hydrophobem Fasermaterial |
| DE2856283A1 (de) * | 1978-12-27 | 1980-07-17 | Cassella Ag | Verfahren zur herstellung von reserveeffekten auf polyester-zellulose-mischfaser-textilien |
| DE3065361D1 (en) * | 1979-07-02 | 1983-11-24 | Hoechst Ag | Two-phase printing process for the manufacture of conversion style and discharge resist articles |
-
1979
- 1979-07-27 DE DE19792930541 patent/DE2930541A1/de not_active Withdrawn
-
1980
- 1980-07-21 DE DE8080104279T patent/DE3065045D1/de not_active Expired
- 1980-07-21 EP EP80104279A patent/EP0023660B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| EP0023660A2 (fr) | 1981-02-11 |
| DE3065045D1 (en) | 1983-11-03 |
| DE2930541A1 (de) | 1981-02-12 |
| EP0023660A3 (en) | 1981-05-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0013378B1 (fr) | Procédé pour la réalisation d'effets de réserve sur des matières textiles fibreuses mixtes polyester-cellulose | |
| EP0029804B1 (fr) | Procédé d'impression ou de teinture par foulardage de matières textiles en fibres cellulosiques ou en mélanges de ces fibres avec des fibres synthétiques, pâtes d'impression ou bains de foulardage pour la mise en oeuvre du procédé | |
| EP0023660A2 (fr) | Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques | |
| DE887636C (de) | Bestaendiges, wasserloesliches Farbstoffpraeparat | |
| EP0021432B1 (fr) | Procédé d'impression en deux phases pour la préparation d'articles de conversion et de rongeant-réserve | |
| DE2926651A1 (de) | Zweiphasendruckverfahren zur herstellung von konversions- und aetzreserveartikeln | |
| DE3235348A1 (de) | Verfahren zum bedrucken von textilmaterial | |
| EP0124086B1 (fr) | Procédé pour réaliser des impressions d'une réserve | |
| EP0062183B1 (fr) | Procédé d'impression à réserve | |
| DE812069C (de) | Verfahren zur Herstellung von echten Drucken | |
| DE574355C (de) | Verfahren zur Herstellung von Drucken oder Buntreserven von unloeslichen Azofarbstoffen auf der Faser neben Drucken oder unter Klotzungen von Kuepenfarbstoffen aus Estersalzen von Leukokuepenfarbstoffen | |
| DE228694C (fr) | ||
| AT40419B (de) | Verfahren zur Herstellung von Chromlacken der Beizenfarbstoffe auf der Faser. | |
| AT62838B (de) | Verfahren zum Drucken von Küpenfarbstoffen der Anthrachinonreihe. | |
| DE208998C (fr) | ||
| DE3841482A1 (de) | Einphasen-verfahren zur herstellung von drucken mit reaktivfarbstoffen neben azo-entwicklungsfarbstoffen auf alkalisch vorgrundierten textilien | |
| DE1810306B2 (de) | Verfahren zur herstellung von reserveeffekten mit reaktivfarbstoffen unter reaktivfarbstoffen oder aus mischungen von reaktivfarbstoffen unterschiedlicher fixierbarkeit | |
| DE622976C (de) | Verfahren zur Herstellung von Azofarbstoffen auf Cellulosefasern | |
| DE1810307C3 (de) | Verfahren zur Herstellung von Reserveeffekten unter Färbungen oder Drucken mit Dispersionsfarbstoffen auf textlien Flächengebilden aus Synthesefasern | |
| DE3430006A1 (de) | Verfahren zum drucken mit reaktiv- und dispersionsfarbstoffen | |
| DE578649C (de) | Verfahren zur Herstellung von Vordruckreserven unter Oxydationsfarbstoffen, namentlich Anilinschwarz | |
| DE267408C (fr) | ||
| AT33316B (de) | Verfahren zur Herstellung von Ätzreserven unter Küpenfarbstoffen auf mittelst Hydrosulfiten ätzbaren Färbungen. | |
| DE197150C (fr) | ||
| DE626686C (de) | Verfahren zum Reservieren von Faerbungen aus Estersalzen von Leukokuepenfarbstoffen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Designated state(s): CH DE FR GB IT |
|
| PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
| AK | Designated contracting states |
Designated state(s): CH DE FR GB IT |
|
| 17P | Request for examination filed |
Effective date: 19811009 |
|
| ITF | It: translation for a ep patent filed | ||
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Designated state(s): CH DE FR GB IT LI |
|
| REF | Corresponds to: |
Ref document number: 3065045 Country of ref document: DE Date of ref document: 19831103 |
|
| ET | Fr: translation filed | ||
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Effective date: 19840731 Ref country code: CH Effective date: 19840731 |
|
| PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
| 26N | No opposition filed | ||
| GBPC | Gb: european patent ceased through non-payment of renewal fee | ||
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19850329 |
|
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19850402 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19881118 |