EP0080642A1 - Procédé de teinture - Google Patents
Procédé de teinture Download PDFInfo
- Publication number
- EP0080642A1 EP0080642A1 EP82110546A EP82110546A EP0080642A1 EP 0080642 A1 EP0080642 A1 EP 0080642A1 EP 82110546 A EP82110546 A EP 82110546A EP 82110546 A EP82110546 A EP 82110546A EP 0080642 A1 EP0080642 A1 EP 0080642A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dye
- liquors
- parts
- radical
- dyeing
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 28
- 238000004043 dyeing Methods 0.000 title claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- 239000000975 dye Substances 0.000 claims description 29
- 239000000835 fiber Substances 0.000 claims description 17
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 14
- 229920003043 Cellulose fiber Polymers 0.000 claims description 8
- 239000000985 reactive dye Substances 0.000 claims description 8
- 239000011780 sodium chloride Substances 0.000 claims description 8
- 239000004952 Polyamide Substances 0.000 claims description 7
- 229920002647 polyamide Polymers 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- 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 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 239000001488 sodium phosphate Substances 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 229910000403 monosodium phosphate Inorganic materials 0.000 claims description 3
- 235000019799 monosodium phosphate Nutrition 0.000 claims description 3
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000000732 arylene group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910000402 monopotassium phosphate Inorganic materials 0.000 claims description 2
- 235000019796 monopotassium phosphate Nutrition 0.000 claims description 2
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims 2
- JTNCEQNHURODLX-UHFFFAOYSA-N 2-phenylethanimidamide Chemical compound NC(=N)CC1=CC=CC=C1 JTNCEQNHURODLX-UHFFFAOYSA-N 0.000 claims 1
- 229910021538 borax Inorganic materials 0.000 claims 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 claims 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 claims 1
- 235000019797 dipotassium phosphate Nutrition 0.000 claims 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims 1
- 229910000397 disodium phosphate Inorganic materials 0.000 claims 1
- 235000019800 disodium phosphate Nutrition 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 235000011056 potassium acetate Nutrition 0.000 claims 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 claims 1
- 239000011833 salt mixture Substances 0.000 claims 1
- 235000015424 sodium Nutrition 0.000 claims 1
- 239000001632 sodium acetate Substances 0.000 claims 1
- 235000017281 sodium acetate Nutrition 0.000 claims 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 claims 1
- 235000010339 sodium tetraborate Nutrition 0.000 claims 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 claims 1
- -1 glycidyl radical Chemical class 0.000 description 32
- 235000002639 sodium chloride Nutrition 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 239000002964 rayon Substances 0.000 description 4
- 210000002268 wool Anatomy 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical group 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000013505 freshwater Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000009981 jet dyeing Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000009970 yarn dyeing Methods 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
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
- 150000008043 acidic salts Chemical class 0.000 description 1
- 239000003513 alkali 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
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- HTHKZOCCOVYKKI-UHFFFAOYSA-N dinaphthalen-1-ylmethanedisulfonic acid;sodium Chemical compound [Na].C1=CC=C2C(C(C=3C4=CC=CC=C4C=CC=3)(S(=O)(=O)O)S(O)(=O)=O)=CC=CC2=C1 HTHKZOCCOVYKKI-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 238000009975 hank dyeing Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000979 synthetic dye Substances 0.000 description 1
- 239000004753 textile 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
- D06P3/82—Textiles which contain different kinds of fibres
- D06P3/8204—Textiles which contain different kinds of fibres fibres of different chemical nature
- D06P3/8223—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups
- D06P3/8238—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups using different kinds of dye
- D06P3/8252—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups using different kinds of dye using dispersed and reactive dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/0056—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres
- D06P1/0064—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres by using reactive polyfunctional compounds, e.g. crosslinkers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/10—Material containing basic nitrogen containing amide groups using reactive 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
- 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
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
- D06P3/66—Natural or regenerated cellulose using reactive dyes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/917—Wool or silk
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/924—Polyamide fiber
Definitions
- the present invention relates to a new dyeing process based on the pull-out principle.
- the process according to the invention is characterized in that dye liquors are used which, in addition to the dye or a dye mixture, contain one or more salts, at least one compound containing a glycidyl radical and, if appropriate, further auxiliaries.
- the process of the invention is particularly suitable for dyeing cellulose fiber materials and / or polyamide materials and cellulose fiber materials and / or fiber mixtures containing reactive dyes using the pull-out principle.
- Suitable salts in the process according to the invention are primarily neutral reacting salts, optionally in a mixture with weakly acidic or weakly alkaline reacting salts.
- Q is only zero if m and n are zero and the glycidyl radical is bound to a heteroatom of Z.
- the bridge member Y is preferably bonded to a nitrogen atom of Z.
- the aliphatic and cycloaliphatic hydrocarbon radicals are, in particular, optionally branched radicals having up to 8 carbon atoms.
- Preferred aliphatic radicals Z and preferred alkyl radicals R and R 1 are those having 1-5 carbon atoms.
- Preferred cycloaliphatic radicals Z and cycloalkyl radicals R 1 are the cyclopentyl and the cyclohexyl radical.
- Aryl or aralkyl are especially phenyl or benzyl.
- A stands for example for a C 2 -C 6 alkylene or a phenylene radical.
- heterocyclic radicals Z are the 1,3,5-hexahydrotriazine radical or radicals of the formula called, wherein R 2 for hydrogen or together for oxygen, R 3 for hydrogen or methyl and B for or -CH 2 - stand, or the grouping represents an o-phenylene radical.
- the compounds containing glycidyl groups are alcohols, their esters with acids, e.g. with phosphoric acid.
- the amounts of compounds containing glycidyl radical to be used by the process according to the invention depend on the depth of color to be achieved and the liquor ratio.
- the following reactive dye classes are preferably suitable as dyes suitable for the process according to the invention for dyeing cellulose: organic dyes from the series of the anthraquinone, azo, azo metal complex series, formazane, oxazine and phthalocyanine series, the at least one fiber-reactive group such as the sulfatoethylsulfonyl , Monochlorotriazinyl, dichlorotriazinyl, dichloroquinoxalinyl, trichloropyrimidinyl, monofluorotriazinyl, 2,4-difluoro-5-chloropyrimidinyl, 2-fluoro-5-chloro-6-methylpyrimidinyl, 4-fluoro-5-chloropyrimidinyl group .
- Fibers are used to dye the non-cellulose portion of the respective mixed fiber using the dyes customary for the corresponding fiber, such as, for example, dispersion dyes, in the usual concentration ratios.
- the dyes customary for the corresponding fiber such as, for example, dispersion dyes, in the usual concentration ratios.
- the process according to the invention is particularly suitable for dyeing cellulose fibers and fibers containing cellulose.
- cellulose fibers cotton, rayon, rayon.
- polyester fibers The following fibers are listed as a mixture with cellulose: polyester fibers, polyamide fibers.
- the method according to the invention is also suitable for dyeing wool or wool in a mixture with other fibers such as e.g. Acrylate, polyester, polyamide fibers.
- the starting pH value and the amount and type of auxiliary substances which may have been added should be selected.
- auxiliaries are: leveling agents, dispersants, antioxidants, carrier substances, etc.
- the amounts of salt to be used depend on the color depth and the desired dyeing temperature or the liquor ratio, and can be determined in a simple manner by preliminary use.
- the saise used in the process according to the invention can also be used alone and / or in a mixture.
- Mixtures of 30 to 120 g / l, preferably 50-80 g / l of a neutral salt such as sodium chloride or sodium sulfate with 0.2 to 4 g / 1 of a weakly alkaline or weakly acidic reaction have proven to be advantageous.
- the initial pH of the dye bath depends on the tissue to be dyed.
- suitable for setting the desired initial pH value suitable for setting the desired initial pH value. Addition of weak acids like acetic acid.
- an initial pH of the dye liquor which is between pH 5 and pH 8 (in particular between pH 6.5 and 7.5).
- the final pH of the above-mentioned dye liquors is then from pH 8 to pH 11.5, preferably from pH 9.5 to 10.5.
- dyeing wool one selects an initial pH value between pH 2 and pH 5, the final pH value then being between pH 5 and pH 7.
- the added glycidyl compound leads to a continuous increase in pH with increasing temperature, the increase profile of which depends on various factors, e.g. also depends on the reaction of the reactive dye with the cellulose fiber and on the type of glycidyl compound used.
- glycidyl compounds are added to the dye liquors used which, when they are cleaved, first release alkali and then acid (e.g. esters from alcohols containing phosphoric acid and glycidyl groups, in which case the pH of the dye liquor initially rises slowly and thus favors a dyeing of the cellulose or polyamide portion of the fiber, the pH then finally falling again due to the slowly released phosphoric acid and fostering of the other portion of the fiber (eg polyester) in the acidic range).
- the pH range therefore rises from pH 5 to 8 to values around pH 8-10 and then falls towards the end of the dyeing process without addition of acid at temperatures from 80 to 130 ° C to values from pH 5 to pH 7.
- the process according to the invention is generally carried out in such a way that the initial temperatures are between 20 and 40 ° C. and the final temperatures between 45 and 125 ° C.
- the process can advantageously also be carried out at a constant temperature, for example at 65 °.
- 100 parts of a mercerized cotton yarn are placed in the form of cross-wound bobbins on the yarn dyeing machine in 1000 parts of a liquor consisting of 90 parts of common salt, 8 parts of the compound of the formula 2 parts of dye II and 900 parts of water.
- the initial pH of the liquor is 6.9.
- the liquor is heated at a rate of 1/2 ° / min. heated to 95 ° C and 15 min. kept at this temperature.
- the final pH of the liquor is 9.2.
- the exhausted remaining liquor is then drained off and the dyeing obtained is rinsed cold and warm and, as usual, for 10 minutes. cooked with fresh water. A clear blue color is obtained.
- the initial pH of the liquor is 7.5. It will be in 60 min. warmed to 95 ° C and dyed at this temperature for 1 hour. The pH of the liquor slowly rises to pH 9.2 and then gradually drops to 6.5.
- the initial pH of the liquor is 8.2. It is dyed at 60 ° C for 2 hours. During this time, the pH slowly increases to 11.3. After the usual rinsing and boiling soaps you get a level, deep green color with good fastness properties.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Structural Engineering (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813147153 DE3147153A1 (de) | 1981-11-27 | 1981-11-27 | Faerbeverfahren |
| DE3147153 | 1981-11-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0080642A1 true EP0080642A1 (fr) | 1983-06-08 |
| EP0080642B1 EP0080642B1 (fr) | 1986-10-15 |
Family
ID=6147396
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP82110546A Expired EP0080642B1 (fr) | 1981-11-27 | 1982-11-16 | Procédé de teinture |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4439206A (fr) |
| EP (1) | EP0080642B1 (fr) |
| JP (1) | JPS5891876A (fr) |
| DE (2) | DE3147153A1 (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59116482A (ja) * | 1982-12-23 | 1984-07-05 | 住友化学工業株式会社 | 混用繊維材料の染色法 |
| JPS63315680A (ja) * | 1987-06-17 | 1988-12-23 | 日本サ−ファクタント工業株式会社 | 反応性染料用均染剤及び染色方法 |
| EP0620311B1 (fr) * | 1993-04-15 | 1998-02-11 | Nippon Sanmo Sensyoku Co.,Ltd. | Laine modifiée et procédé pour rendre la laine non rétrécissable |
| US5655936A (en) * | 1995-12-18 | 1997-08-12 | Yazaki Corporation | Self locking, constant pressure electrical terminal for threaded studs |
| US6066183A (en) * | 1998-04-13 | 2000-05-23 | I-Hwa Industrial Co., Ltd. | Liquid dispersed dye of the azo or anthraquinone type |
| US6520384B2 (en) * | 2001-04-30 | 2003-02-18 | Ketan C. Mehta | Apparatus and method for nasal rinse |
| USD627458S1 (en) | 2009-12-16 | 2010-11-16 | Water Pik, Inc. | Vessel for sinus cavity rinse |
| USD676126S1 (en) | 2010-06-25 | 2013-02-12 | Water Pik, Inc. | Faceted nasal seal |
| US9061096B2 (en) | 2009-12-16 | 2015-06-23 | Water Pik, Inc. | Powered irrigator for sinus cavity rinse |
| USD676125S1 (en) | 2010-06-25 | 2013-02-12 | Water Pik, Inc. | Faceted nasal seal with bottom rim |
| USD629884S1 (en) | 2009-12-16 | 2010-12-28 | Water Pik, Inc. | Powered irrigator for sinus cavity rinse |
| USD653953S1 (en) | 2009-12-16 | 2012-02-14 | Water Pik, Inc. | Squeeze bottle |
| US8888752B2 (en) * | 2009-12-16 | 2014-11-18 | Water Pik, Inc. | Bottle for sinus cavity rinse |
| US8486029B2 (en) * | 2009-12-16 | 2013-07-16 | Water Pik, Inc. | Pot for sinus cavity rinse |
| USD634630S1 (en) | 2009-12-16 | 2011-03-22 | Water Pik, Inc. | Nozzle |
| USD634631S1 (en) | 2009-12-16 | 2011-03-22 | Water Pik, Inc. | Nozzle and collar |
| USD630314S1 (en) | 2009-12-16 | 2011-01-04 | Water Pik, Inc. | Vessel with handle for sinus cavity rinse |
| US8991660B2 (en) * | 2009-12-16 | 2015-03-31 | Water Pik, Inc. | Squeeze bottle for sinus cavity rinse |
| EP2534206B1 (fr) * | 2010-02-09 | 2014-04-02 | Unilever PLC | Polymères colorants |
| US8409152B2 (en) | 2010-06-25 | 2013-04-02 | Water Pik, Inc. | Faceted nasal seal |
| USD670373S1 (en) | 2010-12-16 | 2012-11-06 | Water Pik, Inc. | Powered irrigator for sinus cavity rinse |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE503812C (de) * | 1925-12-10 | 1930-08-08 | I G Farbenindustrie Akt Ges | Verfahren zur Darstellung farbiger Kondensationsprodukte von Kuepenfarbstoffen |
| FR1216308A (fr) * | 1957-09-25 | 1960-04-25 | Ciba Geigy | Procédé de teinture de matières polyhydroxylées |
| DE1239266B (de) * | 1962-04-28 | 1967-04-27 | Basf Ag | Verfahren zum Faerben und bzw. oder Bedrucken von Textilgut |
| US3501259A (en) * | 1958-10-28 | 1970-03-17 | American Cyanamid Co | Process for simultaneous coloration and finishing of cellulose fibers and reactive dyes therefor |
| DE1619464A1 (de) * | 1966-02-23 | 1970-10-29 | Hoechst Ag | Verfahren zum Faerben von Cellulosefasern mit Reaktivfarbstoffen oder von Mischungen aus Cellulose- und Polyesterfasern mit Reaktiv- und Dispersionsfarbstoffen |
| DE2020917A1 (de) * | 1969-05-07 | 1970-11-19 | Ciba Geigy | Zubereitungen von Polyadditionsprodukten,Verfahren zu deren Herstellung und Verwendung |
| GB1236882A (en) * | 1968-09-25 | 1971-06-23 | Manuf De Prod Chim Protex | Improvement in methods of dyeing and printing textile fibres |
| GB2028876A (en) * | 1978-09-01 | 1980-03-12 | Bayer Ag | Process for dyeing and printing cellulose fibres with reactive dyestuffs |
| EP0021044A1 (fr) * | 1979-06-01 | 1981-01-07 | Bayer Ag | Procédé de teinture de fibres cellulosiques et de mélanges fibreux contenant des fibres cellulosiques avec des colorants réactifs |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3673558A (en) * | 1970-05-04 | 1972-06-27 | Ciba Ltd | Polyaddition products and process for their manufacture |
| DE2914142A1 (de) * | 1979-04-07 | 1980-11-13 | Bayer Ag | Verfahren zum einbadigen, einstufigen faerben oder bedrucken von cellulosefasern mit faserreaktiven dispersionsfarbstoffen |
| DE2838274A1 (de) * | 1978-09-01 | 1980-03-13 | Bayer Ag | Verfahren zum faerben und bedrucken von cellulosefasern mit reaktivfarbstoffen |
-
1981
- 1981-11-27 DE DE19813147153 patent/DE3147153A1/de not_active Withdrawn
-
1982
- 1982-11-03 US US06/439,099 patent/US4439206A/en not_active Expired - Fee Related
- 1982-11-16 DE DE8282110546T patent/DE3273813D1/de not_active Expired
- 1982-11-16 EP EP82110546A patent/EP0080642B1/fr not_active Expired
- 1982-11-24 JP JP57204720A patent/JPS5891876A/ja active Pending
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE503812C (de) * | 1925-12-10 | 1930-08-08 | I G Farbenindustrie Akt Ges | Verfahren zur Darstellung farbiger Kondensationsprodukte von Kuepenfarbstoffen |
| FR1216308A (fr) * | 1957-09-25 | 1960-04-25 | Ciba Geigy | Procédé de teinture de matières polyhydroxylées |
| US3501259A (en) * | 1958-10-28 | 1970-03-17 | American Cyanamid Co | Process for simultaneous coloration and finishing of cellulose fibers and reactive dyes therefor |
| DE1239266B (de) * | 1962-04-28 | 1967-04-27 | Basf Ag | Verfahren zum Faerben und bzw. oder Bedrucken von Textilgut |
| DE1619464A1 (de) * | 1966-02-23 | 1970-10-29 | Hoechst Ag | Verfahren zum Faerben von Cellulosefasern mit Reaktivfarbstoffen oder von Mischungen aus Cellulose- und Polyesterfasern mit Reaktiv- und Dispersionsfarbstoffen |
| GB1236882A (en) * | 1968-09-25 | 1971-06-23 | Manuf De Prod Chim Protex | Improvement in methods of dyeing and printing textile fibres |
| DE2020917A1 (de) * | 1969-05-07 | 1970-11-19 | Ciba Geigy | Zubereitungen von Polyadditionsprodukten,Verfahren zu deren Herstellung und Verwendung |
| GB2028876A (en) * | 1978-09-01 | 1980-03-12 | Bayer Ag | Process for dyeing and printing cellulose fibres with reactive dyestuffs |
| EP0021044A1 (fr) * | 1979-06-01 | 1981-01-07 | Bayer Ag | Procédé de teinture de fibres cellulosiques et de mélanges fibreux contenant des fibres cellulosiques avec des colorants réactifs |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3147153A1 (de) | 1983-06-01 |
| DE3273813D1 (en) | 1986-11-20 |
| JPS5891876A (ja) | 1983-05-31 |
| EP0080642B1 (fr) | 1986-10-15 |
| US4439206A (en) | 1984-03-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0080642A1 (fr) | Procédé de teinture | |
| EP0347685B1 (fr) | Mélanges de colorants de dispersion bleus | |
| EP0545207A1 (fr) | Mélange de colorants réactifs ayant des caractéristiques de combinaison améliorées | |
| EP0044483B1 (fr) | Procédé de teinture réactive | |
| DE2914111C2 (de) | Verfahren zum Färben von Cellulosematerialien mit Reaktivfarbstoffen nach dem Ausziehverfahren | |
| DE2803309A1 (de) | Textilbehandlungsverfahren unter verwendung organischer saeurespender | |
| EP0023341B1 (fr) | Adjuvant de foulardage, procédé pour sa préparation et procédé de teinture de fibres cellulosiques resp. de mélanges de fibres cellulosiques avec des fibres synthétiques avec des colorants au soufre, des colorants de cuve au soufre, des colorants de cuve et des colorants réactifs | |
| EP0742270B1 (fr) | Mélange de colorants réactifs de phtalocyanine | |
| DE2835035A1 (de) | Verfahren zum faerben von cellulosefasern mit reaktivfarbstoffen nach der ausziehmethode | |
| EP0596323A2 (fr) | Mélange de colorants de phtalocyanine réactifs | |
| EP0330967A2 (fr) | Procédé de teinture de matières fibreuses synthétiques | |
| EP0093935A1 (fr) | Mélanges de colorants | |
| EP0062865B1 (fr) | Procédé de teinture | |
| EP0379872A1 (fr) | Procédé pour colorer des produits synthétiques en fibres | |
| EP0273300A2 (fr) | Procédé de teinture en un seul bain et une seule étape de mélanges de fibres en polyester pouvant être teintes sans véhiculeur et de fibres cellulosiques | |
| DE4441369A1 (de) | Mischungen von Azofarbstoffen für schwarze Farbtöne | |
| DE3427806C2 (fr) | ||
| DE2108876C3 (de) | Verfahren zum einbadigen Färben von Mischungen aus Cellulose- und Polyamidfasern nach der Ausziehmethode | |
| DE2607007A1 (de) | Farbstoffverbindungen, verfahren zu deren herstellung und verwendung derselben | |
| EP0045068A1 (fr) | Procédé de teinture en semi-continu de matières constituées de fibres cellulosiques, tricotées sur métiers circulaires, utilisant des colorants de développement azoiques | |
| EP0264346A1 (fr) | Procédé de teinture de matières fibreuses en polyamides naturels ou synthétiques avec des colorants à complexes métallifères 1:1 | |
| DE2512520C2 (de) | Verfahren zum faerben von cellulosefasern, stickstoffhaltigen fasern, synthetischen fasern und deren mischungen | |
| DE1801715C3 (de) | Verfahren zum einbadigen Färben von Mischungen aus Cellulose-, Polyester- und Polyacrylnitrilfasern | |
| DE1619513C (de) | Verfahren zum Färben von Mischungen aus Cellulose- und Polyesterfasern | |
| DE3801112A1 (de) | Verfahren zum faerben von cellulosefasermaterialien |
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 |
|
| 17P | Request for examination filed |
Effective date: 19821116 |
|
| AK | Designated contracting states |
Designated state(s): CH DE FR GB IT LI |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): CH DE FR GB IT LI |
|
| ET | Fr: translation filed | ||
| REF | Corresponds to: |
Ref document number: 3273813 Country of ref document: DE Date of ref document: 19861120 |
|
| ITF | It: translation for a ep patent filed | ||
| 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 | ||
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19881116 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Effective date: 19881130 Ref country code: CH Effective date: 19881130 |
|
| 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: 19890731 |
|
| 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: 19890801 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |