EP0017618B1 - Procédé d'azurage optique de fibres en polyester par épuisement du bain - Google Patents
Procédé d'azurage optique de fibres en polyester par épuisement du bain Download PDFInfo
- Publication number
- EP0017618B1 EP0017618B1 EP80810098A EP80810098A EP0017618B1 EP 0017618 B1 EP0017618 B1 EP 0017618B1 EP 80810098 A EP80810098 A EP 80810098A EP 80810098 A EP80810098 A EP 80810098A EP 0017618 B1 EP0017618 B1 EP 0017618B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dispersion
- process according
- fluorescent whitening
- whitening agent
- dye
- 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 32
- 229920000728 polyester Polymers 0.000 title claims description 25
- 238000005282 brightening Methods 0.000 title description 10
- 239000006185 dispersion Substances 0.000 claims description 32
- 239000000975 dye Substances 0.000 claims description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 239000002270 dispersing agent Substances 0.000 claims description 11
- 238000004043 dyeing Methods 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 7
- 239000000986 disperse dye Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 4
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims description 3
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- 239000006081 fluorescent whitening agent Substances 0.000 claims 8
- NGQSLSMAEVWNPU-UHFFFAOYSA-N 1,2-bis(2-phenylethenyl)benzene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1C=CC1=CC=CC=C1 NGQSLSMAEVWNPU-UHFFFAOYSA-N 0.000 claims 1
- GLIKXZUJKIVGIE-UHFFFAOYSA-N 2-[2-(2-phenylethenyl)phenyl]-1,3-benzoxazole Chemical compound C=1C=CC=C(C=2OC3=CC=CC=C3N=2)C=1C=CC1=CC=CC=C1 GLIKXZUJKIVGIE-UHFFFAOYSA-N 0.000 claims 1
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 claims 1
- 229960002218 sodium chlorite Drugs 0.000 claims 1
- 230000002087 whitening effect Effects 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 18
- 239000000835 fiber Substances 0.000 description 15
- -1 aromatic halogenated hydrocarbons Chemical class 0.000 description 10
- 230000003287 optical effect Effects 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 238000004061 bleaching Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 4
- 235000021286 stilbenes Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 3
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- ZUBJEHHGZYTRPH-KTKRTIGZSA-N [(z)-octadec-9-enyl] hydrogen sulfate Chemical compound CCCCCCCC\C=C/CCCCCCCCOS(O)(=O)=O ZUBJEHHGZYTRPH-KTKRTIGZSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical class ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- DQBNLFRFALCILS-UHFFFAOYSA-N 1-[(2-sulfonaphthalen-1-yl)methyl]naphthalene-2-sulfonic acid Chemical compound C1=CC=C2C(CC3=C4C=CC=CC4=CC=C3S(=O)(=O)O)=C(S(O)(=O)=O)C=CC2=C1 DQBNLFRFALCILS-UHFFFAOYSA-N 0.000 description 1
- LWEAHXKXKDCSIE-UHFFFAOYSA-N 2,3-di(propan-2-yl)naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(C(C)C)C(C(C)C)=CC2=C1 LWEAHXKXKDCSIE-UHFFFAOYSA-N 0.000 description 1
- QZEDXQFZACVDJE-UHFFFAOYSA-N 2,3-dibutylnaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 QZEDXQFZACVDJE-UHFFFAOYSA-N 0.000 description 1
- CHZLVSBMXZSPNN-UHFFFAOYSA-N 2,4-dimethylbenzenesulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C(C)=C1 CHZLVSBMXZSPNN-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- RBABXJPJIHMBBP-WXUKJITCSA-N 2-[(e)-2-[4-[(e)-2-(2-cyanophenyl)ethenyl]phenyl]ethenyl]benzonitrile Chemical compound N#CC1=CC=CC=C1\C=C\C(C=C1)=CC=C1\C=C\C1=CC=CC=C1C#N RBABXJPJIHMBBP-WXUKJITCSA-N 0.000 description 1
- WFYSPVCBIJCZPX-UHFFFAOYSA-N 2-[4-(1,3-benzoxazol-2-yl)naphthalen-1-yl]-1,3-benzoxazole Chemical compound C12=CC=CC=C2C(C=2OC3=CC=CC=C3N=2)=CC=C1C1=NC2=CC=CC=C2O1 WFYSPVCBIJCZPX-UHFFFAOYSA-N 0.000 description 1
- UGFSLKRMHPGLFU-UHFFFAOYSA-N 2-[5-(1,3-benzoxazol-2-yl)thiophen-2-yl]-1,3-benzoxazole Chemical compound C1=CC=C2OC(C3=CC=C(S3)C=3OC4=CC=CC=C4N=3)=NC2=C1 UGFSLKRMHPGLFU-UHFFFAOYSA-N 0.000 description 1
- CBCZQJLYYRPMRI-UHFFFAOYSA-N 2-benzylnaphthalene-1-sulfonic acid Chemical compound C1=CC2=CC=CC=C2C(S(=O)(=O)O)=C1CC1=CC=CC=C1 CBCZQJLYYRPMRI-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- XNOVXSVWOMRJCP-UHFFFAOYSA-N 2-hexyl-3-propylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CCCCCC)=C(CCC)C=C21 XNOVXSVWOMRJCP-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
- DLHGMUSMPXAUDH-UHFFFAOYSA-N 4-[2-(5,6-dimethyl-1,3-benzoxazol-2-yl)ethenyl]benzonitrile Chemical compound O1C=2C=C(C)C(C)=CC=2N=C1C=CC1=CC=C(C#N)C=C1 DLHGMUSMPXAUDH-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 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
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229910001919 chlorite Inorganic materials 0.000 description 1
- 229910052619 chlorite group Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000004816 dichlorobenzenes Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000010327 methods by industry Methods 0.000 description 1
- QLAXRNXBCBELEB-UHFFFAOYSA-N methyl 4-[2-(5,6-dimethyl-1,3-benzoxazol-2-yl)ethenyl]benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1C=CC1=NC2=CC(C)=C(C)C=C2O1 QLAXRNXBCBELEB-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001057 purple pigment Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- GIPRGFRQMWSHAK-UHFFFAOYSA-M sodium;2-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=CC=C1S([O-])(=O)=O GIPRGFRQMWSHAK-UHFFFAOYSA-M 0.000 description 1
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002759 woven fabric 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
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
- D06L4/686—Fugitive optical brightening; Discharge of optical brighteners in discharge paste; Blueing; Differential optical brightening
-
- 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
- Y10S8/922—Polyester fiber
Definitions
- the present invention relates to a new, improved process for the optical brightening of polyester fibers in the exhaust process with the aid of conventional polyester brighteners with the use of shading dyes.
- the process according to the invention for the optical brightening of polyester fibers in the drawing-out process by treating the fibers in an aqueous polyester brightener which is stable under the application conditions and which absorbs onto the substrate and a small amount of a blue to violet disperse dye or mixtures of such dyes as shading dye is thereby characterized in that the treatment in said dispersion is carried out at a pH of more than 9.
- the dispersion has a pH between 11 and 14, e.g. B. between 11 and 13.5, in particular between 11 and 12.5.
- the pH is adjusted using a suitable alkaline substance, preferably using alkali metal hydroxides, in particular using KOH, but especially NaOH.
- the treatment is carried out in the customary manner at a temperature between room temperature and 140 ° C., in particular between 50 ° and 130 ° C.
- the fiber material is advantageously used at a lower temperature (for example 50 ° C.), whereupon the temperature is increased (e.g. to 120 ° C).
- HT high temperature
- carrier is added to the treatment bath that is common in dyeing practice.
- carrier addition it is also possible to achieve very good results at lower temperatures, for example below 100 ° C.
- carrier addition can also be used under HT conditions.
- Suitable carriers are those customary in dyeing practice, e.g. B. aromatic hydrocarbons, aromatic halogenated hydrocarbons and esters and ethers of aromatic carboxylic acids.
- Preferred carriers are dichlorobenzenes and trichlorobenzenes, optionally also diphenyl and mixtures of the substances mentioned.
- the duration of the treatment of the textiles in the brightener dispersion can vary within wide limits, but an application period of at least 20 to 30 ° minutes is advantageous.
- the amount of brightener (pure substance) in the dispersion can, depending on the brightener used, vary between 0.002 and 0.5%, based on the material to be lightened.
- the amount of shading dye is, depending on the dye and the desired shade, about 0.0025-2.5%, preferably 0.025-1.25%, based on the amount of brightener (pure substance) used.
- polyester brighteners are used as brighteners, which in practice are applied together with shading dyes. These are mostly benzoxazole, stilbene and naphthalimide brighteners.
- rings A, B and C may also contain simple radicals, such as lower alkyl or alkoxy groups or chlorine atoms, especially 2,5-bis-benzoxazol-2-yl-thiophene, 2,5-bis- (5- Methyl-benzoxazol-2-yl) ethylene and 1,4-bis-benzoxazol-2-yl-naphthalene; or the formula where n is 0 or 1 and rings A and B may be further substituted, e.g. B.
- stilbene brighteners are those of the formulas respectively. wherein the rings A, B and C can carry different substituents, such as. As alkyl, alkoxy, chlorine, cyano, carboxy and its derivatives, etc., to mention, in particular the compounds 2-cyano-4- (naphtho (1,2-d) v-triazol-2-yl) -4'- chlorstilbene, 4- (naphtho [1,2-dlv-triazol-2-yl) -4'-methoxycarbonylstilbene, and 1,4-bis- (2-cyanostyryl) benzene.
- substituents such as alkyl, alkoxy, chlorine, cyano, carboxy and its derivatives, etc.
- naphthalimide brighteners are those of the formula in which R i and R 2 are hydrogen or alkoxy, especially those in which R 1 is hydrogen and R 2 is methoxy or in which R 1 and R 2 are each ethoxy.
- Blue to violet disperse dyes are used as shading dyes, which of course have to be suitable for treatment in an alkaline liquor.
- Acylaminoanthraquinone dyes are preferably used, in particular those of the formula wherein the benzene rings A may be optionally substituted, e.g. B. by alkyl, alkoxy, halogen, etc.
- Dyes whose benzene rings A are unsubstituted or substituted in the para position with chlorine or methoxy are particularly suitable.
- the aqueous dispersion advantageously also contains one or more dispersants and, if appropriate, wetting agents, stabilizers and / or other customary dyeing auxiliaries.
- Suitable dispersants include: alkali metal salts, especially sodium salts of alkyl or alkylarylsulfonic acids and carboxylic acids, alkali metal salts, especially sodium salts of condensation products of arylsulfonic acids with formaldehyde, macromolecular substances which are suitable for liquefaction and dispersion, carboxylates of the polymerized maleic acid type polymerized acrylic acid and copolymers of maleic acid with allyl acetate.
- Examples of such dispersants are: lauryl sulfate sodium salt, oleyl sulfate sodium salt, oleyl sulfate diethanolamine salt, benzylnaphthalenesulfonic acid Na, di- (2-sulfo-1-naphthyl) methane di-Na salt, m-xylenesulfonic acid Na, dodecylbenzenesulfonic acid Na Na salt, dodecylbenzenesulfonic acid, diethanolamine, diisopropylnaphthalenesulfonic acid Na, di-n-butylnaphthalenesulfonic acid Na, n-propyl-n-hexylnaphthalenesulfonic acid Na, N-oleylmethyl taurine Na salt, Na salt of the condensation product of naphthalenesulfonic acid and formaldehyde acid formaldehyde , Benzenesulfonic acid sodium salt, cum
- particularly preferred dispersants are nonionic, water-soluble ethoxylated or propoxylated fatty alcohols and alkylphenols and fatty alcohol polyglycol ethers, for example alkanols, alkenols (C 8 -C 22 ) with different amounts of ethyleneoxy or propyleneoxy groups, alkyl or arylpolyglycol ethers with up to 50 ethyleneoxy or propyleneoxy groups, such as octyl, nonyl or dodecylphenol polyglycol ether.
- the individual components can be introduced separately into the treatment bath, which is already alkaline or is only then adjusted to the desired pH.
- Such dispersions contain brightener and dye in the desired ratio. They are made by adding brightener and dye, preferably made together with a dispersant in a small amount of water. It is advantageous if this dispersion is subjected to grinding (for example in a ball mill) in order to obtain particle sizes of less than 10 ⁇ m, preferably less than 2 ⁇ m.
- this stock dispersion can then be introduced (calculated on the desired amount of brightener in the bath) into the treatment bath, which may also contain a dispersant and / or other auxiliaries.
- the treatment bath which may also contain a dispersant and / or other auxiliaries.
- the bleaching bath can then be bleached directly.
- Sodium chloride is preferably added to the liquor, the alkaline bath is acidified and then heated to about boiling temperature.
- polyester fibers naturally also include polyester fibers in blended fabrics, eg. B. in mixed fabrics polyester / cotton.
- the nuanced lightening of such blended fabrics by the process according to the invention can also be advantageous with the lightening of the cotton content, with the bleaching (e.g. with peroxide) and / or the various conventional finishing and finishing processes (e.g. crease-resistant, wash and wear, soft grip and other equipment) can be combined.
- 0.4 g of the stock dispersion described under a) and 0.2 g of a dispersant are processed into a dispersion with 400 ml of water and the latter is made alkaline with 0.8 ml of NaOH 30%.
- polyester staple fabric (washed and heat-set at 1800 C for 20 seconds) are wound evenly onto bobbin tubes as a fabric tape of approx. 250 x 12 cm and treated with the dispersion just described in an HT dyeing machine.
- the fleet had an initial pH of 11.5.
- the temperature is 50 ° C, after that heated to 130 ° C within 30 minutes and then left at this temperature for 30 minutes.
- the mixture is then cooled to 70 ° C., the liquor is drained off, the fabric is rinsed twice warm and dried in a drying cabinet at 80 ° C. for 5 minutes.
- the lightened fabric has a high degree of whiteness with perfect levelness.
- Example 1b As described in Example 1b), 0.4 g of this stock dispersion is processed into a liquor (pH approx. 11.5) and thus 40 g of polyester staple fabric is lightened in the manner given there.
- the treated fabric also has a high degree of whiteness with perfect levelness.
- polyester brightener used is that of the formula a, you also get a highly lightened polyester fabric of excellent levelness.
- Example 1 a 0.4 g of the stock dispersion described in Example 1 a) and 0.2 g of a dispersant (adduct of 35 ethylene oxide groups with stearyl alcohol) are processed into a dispersion with 400 ml of water and the latter made alkaline with 0.8 ml of NaOH 30%.
- a dispersant adduct of 35 ethylene oxide groups with stearyl alcohol
- polyester staple fabric (washed and heat-set at 180 ° C for 30 seconds) are evenly wound onto bobbin tubes as a fabric tape of approx. 250x12 cm and treated with the dispersion just described in an HT dyeing machine.
- the fleet had an initial pH of 11.5.
- the fabric is introduced at 50 ° C. and the liquor is heated to 120 ° C. in 30 minutes, treated at this temperature for 15 minutes, cooled to 70 ° C., 0.8 g of sodium chloride 80% is added and the liquor is made up with 1 , 4 ml of formic acid 85% to a pH of 3-4.
- the mixture is heated to about 100 ° C. in 20 minutes, treated at this temperature for 30 minutes, then the liquor is drained off, rinsed and dried.
- the piece of fabric is immaculate and has a high degree of whiteness.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Coloring (AREA)
Claims (10)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH291979 | 1979-03-29 | ||
| CH2919/79 | 1979-03-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0017618A1 EP0017618A1 (fr) | 1980-10-15 |
| EP0017618B1 true EP0017618B1 (fr) | 1983-03-02 |
Family
ID=4244560
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP80810098A Expired EP0017618B1 (fr) | 1979-03-29 | 1980-03-24 | Procédé d'azurage optique de fibres en polyester par épuisement du bain |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US4283197A (fr) |
| EP (1) | EP0017618B1 (fr) |
| DE (1) | DE3062164D1 (fr) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4426004A1 (de) * | 1994-07-22 | 1996-01-25 | Basf Ag | Verfahren zum optischen Aufhellen von Polyamiden |
| ATE435271T1 (de) * | 2004-09-23 | 2009-07-15 | Unilever Nv | Zusammensetzungen zur wäschebehandlung |
| GB0421145D0 (en) * | 2004-09-23 | 2004-10-27 | Unilever Plc | Laundry treatment compositions |
| ES2322864T3 (es) * | 2004-09-23 | 2009-06-30 | Unilever N.V. | Composiciones de tratamiento de ropa sucia. |
| DE102004051174A1 (de) * | 2004-10-20 | 2006-05-04 | BSH Bosch und Siemens Hausgeräte GmbH | Beleuchtungsvorrichtung für ein wasserführendes Haushaltsgerät |
| AU2007207050A1 (en) * | 2006-01-18 | 2007-07-26 | Basf Se | Process for the treatment of fiber materials |
| CN101370923B (zh) * | 2006-01-18 | 2012-01-11 | 西巴控股公司 | 处理纤维材料的方法 |
| US20080177089A1 (en) | 2007-01-19 | 2008-07-24 | Eugene Steven Sadlowski | Novel whitening agents for cellulosic substrates |
| WO2009074488A1 (fr) * | 2007-12-10 | 2009-06-18 | Basf Se | Formulation de colorant et procédé pour le traitement de matériaux à base de fibres |
| EP2382299B1 (fr) * | 2009-01-26 | 2013-03-13 | Unilever PLC | Incorporation de colorant dans une composition détergente de traitement du linge |
| US8715368B2 (en) | 2010-11-12 | 2014-05-06 | The Procter & Gamble Company | Thiophene azo dyes and laundry care compositions containing the same |
| ES2544539T3 (es) | 2011-05-26 | 2015-09-01 | Unilever N.V. | Composición líquida para lavandería |
| WO2015112341A1 (fr) * | 2014-01-22 | 2015-07-30 | The Procter & Gamble Company | Composition de traitement de textile |
| CN112853526A (zh) * | 2020-12-30 | 2021-05-28 | 湖北鸿鑫化工有限公司 | 一种提高pp扁丝白度的方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1072348B (de) * | 1956-10-01 | 1960-06-02 | The Procter & Gamble Company, Cincinnati, Ohio (V. St. A.) | Waschmittel |
| US3755201A (en) * | 1971-07-26 | 1973-08-28 | Colgate Palmolive Co | Laundry product containing mixed dye bluing agents |
| DE2727112C3 (de) | 1977-06-16 | 1981-06-04 | Öffentliche Prüfstelle und Textilinstitut für Vertragsforschung e.V., 4150 Krefeld | Verfahren zum Vorreinigen und Färben von textilen Materialien |
-
1980
- 1980-03-17 US US06/130,949 patent/US4283197A/en not_active Expired - Lifetime
- 1980-03-24 DE DE8080810098T patent/DE3062164D1/de not_active Expired
- 1980-03-24 EP EP80810098A patent/EP0017618B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| EP0017618A1 (fr) | 1980-10-15 |
| DE3062164D1 (en) | 1983-04-07 |
| US4283197A (en) | 1981-08-11 |
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