CH102071A - Instrument à indications lumineuses. - Google Patents

Instrument à indications lumineuses.

Info

Publication number: CH102071A
Authority: CH; Switzerland
Prior art keywords: hydroxy; amino; anthraquinone; phenoxy; sep
Prior art date: 1922-04-24

Application number

Other languages

German (de)

English (en)

Inventor

Company American Radium

Original Assignee

Company American Radium

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.)

1922-04-24

Filing date

1922-04-24

Publication date

1923-11-16

1922-04-24 Application filed by Company American Radium filed Critical Company American Radium

1923-11-16 Publication of CH102071A publication Critical patent/CH102071A/fr

Links

239000000975 dye Substances 0.000 claims description 52
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 claims description 18
229950011008 tetrachloroethylene Drugs 0.000 claims description 18
239000000835 fiber Substances 0.000 claims description 14
238000000034 method Methods 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 9
239000003960 organic solvent Substances 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 8
229920002994 synthetic fiber Polymers 0.000 claims description 6
239000001000 anthraquinone dye Substances 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
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
239000004753 textile Substances 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 3
125000005142 aryl oxy sulfonyl group Chemical group 0.000 claims description 2
238000010014 continuous dyeing Methods 0.000 claims description 2
125000004663 dialkyl amino group Chemical group 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
239000004758 synthetic textile Substances 0.000 claims description 2
-1 acetyloxy, propionyloxy Chemical group 0.000 description 54
238000004043 dyeing Methods 0.000 description 17
239000004744 fabric Substances 0.000 description 17
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 12
238000010438 heat treatment Methods 0.000 description 11
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 8
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
238000001035 drying Methods 0.000 description 6
238000009998 heat setting Methods 0.000 description 6
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 6
238000005406 washing Methods 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
239000002657 fibrous material Substances 0.000 description 4
239000000463 material Substances 0.000 description 4
239000005020 polyethylene terephthalate Substances 0.000 description 4
238000001953 recrystallisation Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical class OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 4
239000012209 synthetic fiber Substances 0.000 description 4
LNACINMHAGNLER-UHFFFAOYSA-N 1-amino-4-hydroxy-2-(3-hydroxyphenoxy)anthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC(O)=C1 LNACINMHAGNLER-UHFFFAOYSA-N 0.000 description 3
229920002284 Cellulose triacetate Polymers 0.000 description 3
239000004952 Polyamide Substances 0.000 description 3
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
229920002647 polyamide Polymers 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
229920000139 polyethylene terephthalate Polymers 0.000 description 3
229920000098 polyolefin Polymers 0.000 description 3
229920002635 polyurethane Polymers 0.000 description 3
239000004814 polyurethane Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
WJGDGVNCJLKBJO-UHFFFAOYSA-N 1-amino-4-hydroxy-2-(2-hydroxyphenoxy)anthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC=C1O WJGDGVNCJLKBJO-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
150000007529 inorganic bases Chemical class 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
150000007530 organic bases Chemical class 0.000 description 2
229920000515 polycarbonate Polymers 0.000 description 2
239000004417 polycarbonate Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
JBUBYUZDOUATKW-UHFFFAOYSA-N 1-amino-4-hydroxy-2-(4-hydroxyphenoxy)anthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=C(O)C=C1 JBUBYUZDOUATKW-UHFFFAOYSA-N 0.000 description 1
MHXFWEJMQVIWDH-UHFFFAOYSA-N 1-amino-4-hydroxy-2-phenoxyanthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC=C1 MHXFWEJMQVIWDH-UHFFFAOYSA-N 0.000 description 1
AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 description 1
HDECRAPHCDXMIJ-UHFFFAOYSA-N 2-methylbenzenesulfonyl chloride Chemical compound CC1=CC=CC=C1S(Cl)(=O)=O HDECRAPHCDXMIJ-UHFFFAOYSA-N 0.000 description 1
NQGXOOJUAKCSLM-UHFFFAOYSA-N 2-phenoxyanthracene-9,10-dione Chemical class C=1C=C2C(=O)C3=CC=CC=C3C(=O)C2=CC=1OC1=CC=CC=C1 NQGXOOJUAKCSLM-UHFFFAOYSA-N 0.000 description 1
YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
IVJDJEYBDMAWSA-UHFFFAOYSA-N C(COCCOCCOCCOCCOCCOCCO)O.C(CCCCCCCC)C1=C(C=CC=C1)O Chemical compound C(COCCOCCOCCOCCOCCOCCO)O.C(CCCCCCCC)C1=C(C=CC=C1)O IVJDJEYBDMAWSA-UHFFFAOYSA-N 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
229920004934 Dacron® Polymers 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
ZRSKSQHEOZFGLJ-UHFFFAOYSA-N ammonium adipate Chemical compound [NH4+].[NH4+].[O-]C(=O)CCCCC([O-])=O ZRSKSQHEOZFGLJ-UHFFFAOYSA-N 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
HTWWKYKIBSHDPC-UHFFFAOYSA-N decanoyl decanoate Chemical compound CCCCCCCCCC(=O)OC(=O)CCCCCCCCC HTWWKYKIBSHDPC-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000003438 dodecyl group Chemical group [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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000005027 hydroxyaryl group Chemical group 0.000 description 1
239000005457 ice water Substances 0.000 description 1
238000009413 insulation Methods 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 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
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1

Classifications

- G—PHYSICS
- G04—HOROLOGY
- G04B—MECHANICALLY-DRIVEN CLOCKS OR WATCHES; MECHANICAL PARTS OF CLOCKS OR WATCHES IN GENERAL; TIME PIECES USING THE POSITION OF THE SUN, MOON OR STARS
- G04B19/00—Indicating the time by visual means
- G04B19/30—Illumination of dials or hands
- G04B19/32—Illumination of dials or hands by luminescent substances

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Coloring (AREA)

CH102071D 1922-04-24 1922-04-24 Instrument à indications lumineuses. CH102071A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH102071T		1922-04-24

Publications (1)

Publication Number	Publication Date
CH102071A true CH102071A (fr)	1923-11-16

Family

ID=4360583

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH102071D CH102071A (fr)	1922-04-24	1922-04-24	Instrument à indications lumineuses.

Country Status (1)

Country	Link
CH (1)	CH102071A (fr)

1922
- 1922-04-24 CH CH102071D patent/CH102071A/fr unknown

Publication	Publication Date	Title
EP0511166A1 (fr)	1992-10-28	Procédé de stabilisation photochimique et thermique de matériaux fibreux au polyamide avec un complexe du cuivre affin à la fibre et un diarylamide de l'acide oxalique
CH102071A (fr)	1923-11-16	Instrument à indications lumineuses.
DE1282214B (de)	1968-11-07	Verfahren zur Herstellung von Farbstoffen der Phthaloperinonreihe
EP0023022B1 (fr)	1984-04-11	Composés de coumarine, procédés pour leur fabrication, ainsi que les produits intermédiaires utilisés en soi et leur utilisation pour la teinture ou l'impression de textiles
DE1210504B (de)	1966-02-10	Verfahren zur Herstellung von Anthrachinonfarbstoffen
CH373012A (de)	1963-07-31	Verfahren zur Erzeugung echter Wollfärbungen mit Kupfer- oder Nickelphthalocyaninen
EP0507732B1 (fr)	1995-04-26	Acide oxalique diarylamide asymétrique
DE2005012A1 (de)	1971-08-12	Verfahren zum kontinuierlichen Far ben synthetischer Fasermaterialien
DE2512462C2 (de)	1977-05-12	Verfahren zum bedrucken oder klotzfaerben von polyester, cellulose-triacetat, cellulose 2 1/2 acetat und deren mischungen
DE1793172B2 (de)	1973-09-20	Anthrachinonfarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung
DE1811811A1 (de)	1970-02-19	Verfahren zum Faerben und Bedrucken von Textilmaterial aus synthetischen Polyamiden
DE2327013A1 (de)	1974-12-12	Anthrachinonfarbstoffe
DE2300591C3 (de)	1981-07-23	Verwendung von Nitroanthrachinonen zum Färben und Bedrucken von synthetischen Fasermaterialien
DE2238337C3 (de)	1975-01-02	Verfahren zum kontinuierlichen Färben von synthetischen Fasermaterialien aus organischen Lösemitteln
DE633599C (de)	1936-07-31	Verfahren zur Herstellung von sauren Farbstoffen und Verbindungen der Anthrapyrimidinreihe
DE1943535A1 (de)	1971-03-04	Verfahren zum kontinuierlichen Faerben synthetischer Fasermaterialien
DE2118019C3 (de)	1977-01-13	Ausziehverfahren zum Färben von synthetischen Fasermaterialien
DE2239930A1 (de)	1973-06-14	Verfahren zur faerbung von polyesterfasern
DE2405152A1 (de)	1974-08-15	Verfahren zur herstellung von sulfogruppenhaltige anthrachinonverbindungen
DE2510112C3 (de)	1979-09-06	Marineblaue Monoazo-Dispersionsfarbstoffe
CH159661A (de)	1933-01-31	Verfahren zur Gewinnung eines Gemisches von kristallinischem Silizium, Kaliumsulfid und Aluminiumoxyd aus Gesteinen.
DE1160126B (de)	1963-12-27	Verfahren zur Herstellung von wasserloeslichen Reaktivfarbstoffen der Anthrachinonreihe
DE1184879B (de)	1965-01-07	Verfahren zur Herstellung von 1-Hydroxy-2-brom-4-amino-anthrachinonen
DE1943536A1 (de)	1971-03-04	Verfahren zum kontinuierlichen Faerben synthetischer Fasermaterialien
DE2138866A1 (de)	1972-02-10	Verfahren zur Herstellung von Farbstoffen