JPS5942112B2 - 合成繊維類の染色方法 - Google Patents
合成繊維類の染色方法Info
- Publication number
- JPS5942112B2 JPS5942112B2 JP52045426A JP4542677A JPS5942112B2 JP S5942112 B2 JPS5942112 B2 JP S5942112B2 JP 52045426 A JP52045426 A JP 52045426A JP 4542677 A JP4542677 A JP 4542677A JP S5942112 B2 JPS5942112 B2 JP S5942112B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- fibers
- dyeing
- synthetic fibers
- groups
- 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
- 238000004043 dyeing Methods 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 12
- 229920002994 synthetic fiber Polymers 0.000 title claims description 9
- 239000012209 synthetic fiber Substances 0.000 title claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 10
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000000835 fiber Substances 0.000 description 15
- -1 methoxycarbonylmethyl group Chemical group 0.000 description 13
- 229920000728 polyester Polymers 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 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
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 125000004744 butyloxycarbonyl group Chemical group 0.000 description 2
- 229920006239 diacetate fiber Polymers 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 238000001819 mass spectrum Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 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 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 2
- 229920006304 triacetate fiber Polymers 0.000 description 2
- NKEWBOPVULFSFJ-UHFFFAOYSA-N 1,3-dihydroperimidin-2-one Chemical group C1=CC(NC(O)=N2)=C3C2=CC=CC3=C1 NKEWBOPVULFSFJ-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
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920006306 polyurethane fiber Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/12—Perinones, i.e. naphthoylene-aryl-imidazoles
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Coloring (AREA)
- Photoreceptors In Electrophotography (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52045426A JPS5942112B2 (ja) | 1977-04-20 | 1977-04-20 | 合成繊維類の染色方法 |
| US05/895,948 US4268671A (en) | 1977-04-20 | 1978-04-13 | Fluorescent dyes |
| DE19782816606 DE2816606A1 (de) | 1977-04-20 | 1978-04-17 | Fluoreszierende farbstoffe |
| GB15235/78A GB1582626A (en) | 1977-04-20 | 1978-04-18 | Fluorescent dyes |
| FR7811520A FR2388026A1 (fr) | 1977-04-20 | 1978-04-19 | Colorants fluorescents heterocycliques |
| CH424378A CH638552A5 (de) | 1977-04-20 | 1978-04-20 | Fluoreszierende farbstoffe. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52045426A JPS5942112B2 (ja) | 1977-04-20 | 1977-04-20 | 合成繊維類の染色方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53130383A JPS53130383A (en) | 1978-11-14 |
| JPS5942112B2 true JPS5942112B2 (ja) | 1984-10-12 |
Family
ID=12718946
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52045426A Expired JPS5942112B2 (ja) | 1977-04-20 | 1977-04-20 | 合成繊維類の染色方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4268671A (enExample) |
| JP (1) | JPS5942112B2 (enExample) |
| CH (1) | CH638552A5 (enExample) |
| DE (1) | DE2816606A1 (enExample) |
| FR (1) | FR2388026A1 (enExample) |
| GB (1) | GB1582626A (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6162565A (ja) * | 1984-09-04 | 1986-03-31 | Mitsubishi Chem Ind Ltd | ペリノン系化合物 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3103403A (en) * | 1963-09-10 | Dyeing of polyester fibers with com- | ||
| US2770625A (en) * | 1953-07-21 | 1956-11-13 | Bayer Ag | Anthraquinone dyestuffs |
| DE1215844B (de) * | 1962-10-12 | 1966-05-05 | Basf Ag | Verfahren zur Herstellung von Perimidon-6, 7-dicarbonsaeureimiden |
| DE2238378C3 (de) * | 1972-08-04 | 1975-01-09 | Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt | Perlnonfarbstoffe und Verfahren zu Ihrer Herstellung |
| JPS5225180A (en) * | 1975-08-19 | 1977-02-24 | Mitsubishi Chem Ind | Dyeing method of synthetic fibers |
-
1977
- 1977-04-20 JP JP52045426A patent/JPS5942112B2/ja not_active Expired
-
1978
- 1978-04-13 US US05/895,948 patent/US4268671A/en not_active Expired - Lifetime
- 1978-04-17 DE DE19782816606 patent/DE2816606A1/de not_active Ceased
- 1978-04-18 GB GB15235/78A patent/GB1582626A/en not_active Expired
- 1978-04-19 FR FR7811520A patent/FR2388026A1/fr active Granted
- 1978-04-20 CH CH424378A patent/CH638552A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53130383A (en) | 1978-11-14 |
| GB1582626A (en) | 1981-01-14 |
| FR2388026B1 (enExample) | 1984-09-21 |
| DE2816606A1 (de) | 1978-10-26 |
| FR2388026A1 (fr) | 1978-11-17 |
| CH638552A5 (de) | 1983-09-30 |
| US4268671A (en) | 1981-05-19 |
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