CH362046A - Verfahren zur Entfernung optischer Aufhellmittel von synthetischen Textilfasern - Google Patents

Verfahren zur Entfernung optischer Aufhellmittel von synthetischen Textilfasern

Info

Publication number: CH362046A
Authority: CH; Switzerland
Prior art keywords: fibers; synthetic; parts; liquor; swelling agent
Prior art date: 1959-10-01

Application number

CH7244459A

Other languages

German (de)

English (en)

Inventor

Gottfried Dr Duerig

Wilhelm Dr Geigy

Original Assignee

Ciba Geigy

Priority date (The priority date 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 date listed.)

1959-10-01

Filing date

1959-10-01

Publication date

1962-01-31

1959-10-01 Application filed by Ciba Geigy filed Critical Ciba Geigy

1959-10-01 Priority to CH7244459A priority Critical patent/CH362046A/de

1960-04-22 Priority to ES0257541A priority patent/ES257541A1/es

1962-01-31 Publication of CH362046A publication Critical patent/CH362046A/de

Links

239000000835 fiber Substances 0.000 title claims description 26
238000000034 method Methods 0.000 title claims description 19
229920002994 synthetic fiber Polymers 0.000 title claims description 12
230000003287 optical effect Effects 0.000 title claims description 5
239000004758 synthetic textile Substances 0.000 title claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 27
230000008961 swelling Effects 0.000 claims description 13
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 claims description 8
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 8
239000012209 synthetic fiber Substances 0.000 claims description 8
229920002284 Cellulose triacetate Polymers 0.000 claims description 6
239000004952 Polyamide Substances 0.000 claims description 6
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 claims description 6
229920002647 polyamide Polymers 0.000 claims description 6
229920000915 polyvinyl chloride Polymers 0.000 claims description 6
239000004800 polyvinyl chloride Substances 0.000 claims description 6
229920000728 polyester Polymers 0.000 claims description 5
229920001522 polyglycol ester Polymers 0.000 claims description 4
150000001875 compounds Chemical class 0.000 claims description 3
238000004043 dyeing Methods 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
229920002239 polyacrylonitrile Polymers 0.000 claims description 3
239000007788 liquid Substances 0.000 claims description 2
125000002971 oxazolyl group Chemical group 0.000 claims 1
239000005977 Ethylene Substances 0.000 description 13
239000000203 mixture Substances 0.000 description 13
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 6
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 5
238000009835 boiling Methods 0.000 description 5
238000005282 brightening Methods 0.000 description 5
229940117389 dichlorobenzene Drugs 0.000 description 5
239000002657 fibrous material Substances 0.000 description 5
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 3
239000008149 soap solution Substances 0.000 description 3
RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 2
BMRVLXHIZWDOOK-UHFFFAOYSA-N 2-butylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CCCC)=CC=C21 BMRVLXHIZWDOOK-UHFFFAOYSA-N 0.000 description 2
MMSGPUZNNKBAMN-UHFFFAOYSA-N 3-ethyl-4-hydroxyheptane-2,3,4-tricarboxylic acid Chemical compound CCC(C(O)=O)C(O)(C(O)=O)C(CC)(CC)C(O)=O MMSGPUZNNKBAMN-UHFFFAOYSA-N 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
229960001047 methyl salicylate Drugs 0.000 description 2
-1 oxazole radicals Chemical class 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
DSPHFASHOJAOKN-UHFFFAOYSA-N 1-[(7-oxobenzo[a]phenalen-2-yl)amino]anthracene-9,10-dione Chemical compound C1=CC2=CC(NC3=C4C(=O)C5=CC=CC=C5C(C4=CC=C3)=O)=CC(C=3C(=CC=CC=3)C3=O)=C2C3=C1 DSPHFASHOJAOKN-UHFFFAOYSA-N 0.000 description 1
PHTXBNIMGMVGRA-UHFFFAOYSA-N 1-benzyl-2-heptadecylbenzimidazole Chemical compound CCCCCCCCCCCCCCCCCC1=NC2=CC=CC=C2N1CC1=CC=CC=C1 PHTXBNIMGMVGRA-UHFFFAOYSA-N 0.000 description 1
WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 1
CDMGNVWZXRKJNS-UHFFFAOYSA-N 2-benzylphenol Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1 CDMGNVWZXRKJNS-UHFFFAOYSA-N 0.000 description 1
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
NKBASRXWGAGQDP-UHFFFAOYSA-N 5-chlorosalicylic acid Chemical compound OC(=O)C1=CC(Cl)=CC=C1O NKBASRXWGAGQDP-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical group [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
239000004067 bulking agent Substances 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
AFYCEAFSNDLKSX-UHFFFAOYSA-N coumarin 460 Chemical compound CC1=CC(=O)OC2=CC(N(CC)CC)=CC=C21 AFYCEAFSNDLKSX-UHFFFAOYSA-N 0.000 description 1
239000000986 disperse dye Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
239000000463 material Substances 0.000 description 1
QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical group COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
235000010292 orthophenyl phenol Nutrition 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
229920006149 polyester-amide block copolymer Polymers 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000000344 soap Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000271 synthetic detergent Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
238000005406 washing Methods 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
- D06P5/13—Fugitive dyeing or stripping dyes
- D06P5/138—Fugitive dyeing or stripping dyes fugitive dyeing

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Treatment Of Fiber Materials (AREA)

CH7244459A 1959-10-01 1959-10-01 Verfahren zur Entfernung optischer Aufhellmittel von synthetischen Textilfasern CH362046A (de)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
CH7244459A CH362046A (de)	1959-10-01	1959-10-01	Verfahren zur Entfernung optischer Aufhellmittel von synthetischen Textilfasern
ES0257541A ES257541A1 (es)	1959-10-01	1960-04-22	Procedimiento para el desplazamiento del equilibrio de aclaradores ëpticos entre bano acuoso y fibras sinteticas

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH7244459A CH362046A (de)	1959-10-01	1959-10-01	Verfahren zur Entfernung optischer Aufhellmittel von synthetischen Textilfasern

Publications (1)

Publication Number	Publication Date
CH362046A true CH362046A (de)	1962-01-31

Family

ID=4531794

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH7244459A CH362046A (de)	1959-10-01	1959-10-01	Verfahren zur Entfernung optischer Aufhellmittel von synthetischen Textilfasern

Country Status (2)

Country	Link
CH (1)	CH362046A (es)
ES (1)	ES257541A1 (es)

1959
- 1959-10-01 CH CH7244459A patent/CH362046A/de unknown
1960
- 1960-04-22 ES ES0257541A patent/ES257541A1/es not_active Expired

Also Published As

Publication number	Publication date
ES257541A1 (es)	1960-11-01

Publication	Publication Date	Title
EP0058637A1 (de)	1982-08-25	Stabile Präparation eines Behandlungsmittels für textile Substrate
DE2410824C3 (de)	1980-01-03	Oberflächenaktive Stoffmischung und Verfahren zum Nachwaschen von bedrucktem Textilgut aus Polyesterfasern und Polyesterfasern enthaltenden Mischungen
CH677167B5 (es)	1991-10-31
DE1114461B (de)	1961-10-05	Lichtechte optische Aufheller fuer Polyacrylnitril
DE1006383B (de)	1957-04-18	Verfahren zur Verbesserung der Anfaerbbarkeit von geformten Gebilden aus Polyestern auf Terephthalsaeurebasis
CH362046A (de)	1962-01-31	Verfahren zur Entfernung optischer Aufhellmittel von synthetischen Textilfasern
DE1054198B (de)	1959-04-02	Gefaerbte Wasch- oder Waschhilfsmittel
DE2834412C2 (es)	1988-01-14
DE546406C (de)	1932-03-12	Verfahren zur Darstellung von ester- und saeureamidartigen Kondensationsprodukten
DE1094696B (de)	1960-12-15	Verfahren zum optischen Aufhellen von Materialien aus Polyestern
DE2708449C3 (de)	1981-01-08	Verfahren zum gleichmäßigen Färben von bahnförmigen Textilien aus modifizierten Polyesterfasern auf Baumfärbeapparaten
DE2002285B2 (de)	1973-08-16	Verfahren zum verbessern der textilen und faerberischen eigenschaften von textilmaterialien, die aus polyestern bestehen oder diese enthalten
DE744609C (de)	1944-01-21	Wasch-, Netz-, Dispergier- und Emulgiermittel
DE1039161B (de)	1958-09-18	Verfahren zur Herstellung von Pigmentfarbstoffen der Anthrachinonreihe
DE2124495C3 (de)	1980-10-02	Ausziehverfahren zum Färben von synthetischen Fasermaterialien
DE202006019521U1 (de)	2007-03-08	Waschmittelzusatz
DE2118019C3 (de)	1977-01-13	Ausziehverfahren zum Färben von synthetischen Fasermaterialien
DE1955310A1 (de)	1971-05-13	Verwendung von waessrigen Dispersionen von Mischungen aus Benzoxazol- und Phenyloxazolderivaten zum optischen Aufhellen
DE662092C (de)	1938-07-18	Behandlungsbaeder
DE2040864A1 (de)	1971-03-04	Verfahren zum optischen Aufhellen von organischen Fasersubstraten
AT131584B (de)	1933-01-25	Verfahren zum Waschen von Textilmaterialien.
DE1261105B (de)	1968-02-15	Verfahren zum Faerben von Textilfasern oder -faeden aus hochmolekularen, hydrophoben, organischen Stoffen
AT136197B (de)	1934-01-10	Behandlungsbäder für Materialien aller Art.
AT71149B (de)	1916-02-10	Verfahren zum Färben von Rohware, insbesondere mit substantiven Farbstoffen.
DE887861C (de)	1953-08-27	Schmaelzmittel