SU448654A3 - Способ крашени полиамидных и шерст ных волокон - Google Patents
Способ крашени полиамидных и шерст ных волоконInfo
- Publication number
- SU448654A3 SU448654A3 SU1649124A SU1649124A SU448654A3 SU 448654 A3 SU448654 A3 SU 448654A3 SU 1649124 A SU1649124 A SU 1649124A SU 1649124 A SU1649124 A SU 1649124A SU 448654 A3 SU448654 A3 SU 448654A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- wool
- formula
- complexes
- dyeing
- wool fibers
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 11
- 239000000835 fiber Substances 0.000 title description 10
- 210000002268 wool Anatomy 0.000 title description 10
- 238000004043 dyeing Methods 0.000 title description 9
- 239000004952 Polyamide Substances 0.000 title description 8
- 229920002647 polyamide Polymers 0.000 title description 8
- 239000000975 dye Substances 0.000 description 16
- 229910001385 heavy metal Inorganic materials 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- -1 monoazo compound Chemical class 0.000 description 3
- 125000000542 sulfonic acid group Chemical group 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000000536 complexating effect Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 2
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- DMLAVOWQYNRWNQ-UHFFFAOYSA-N azobenzene Chemical compound C1=CC=CC=C1N=NC1=CC=CC=C1 DMLAVOWQYNRWNQ-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 238000009988 textile finishing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/69—Two or more oxygen atoms
-
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
- C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
- C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
- C09B29/3617—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
- C09B29/3621—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring
- C09B29/3626—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O)
-
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/12—Disazo dyes from other coupling components "C"
- C09B31/14—Heterocyclic components
- C09B31/153—Heterocyclic components containing a six-membered ring with one nitrogen atom as the only ring hetero-atom
-
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
- C09B35/10—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type
- C09B35/18—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type from heterocyclic compounds
- C09B35/185—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type from heterocyclic compounds from pyridine or pyridone components
-
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/025—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups of azo-pyridone series
-
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/002—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
- C09B62/006—Azodyes
- C09B62/0067—Azodyes with heterocyclic compound as coupling component
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH607170A CH561757A5 (enExample) | 1970-04-23 | 1970-04-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU448654A3 true SU448654A3 (ru) | 1974-10-30 |
Family
ID=4303765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1649124A SU448654A3 (ru) | 1970-04-23 | 1971-04-23 | Способ крашени полиамидных и шерст ных волокон |
Country Status (13)
| Country | Link |
|---|---|
| AT (1) | AT304720B (enExample) |
| BE (1) | BE766181A (enExample) |
| BR (1) | BR7102444D0 (enExample) |
| CA (1) | CA970773A (enExample) |
| CH (1) | CH561757A5 (enExample) |
| CS (1) | CS176156B2 (enExample) |
| DD (1) | DD96245A5 (enExample) |
| DE (1) | DE2118945C2 (enExample) |
| FR (1) | FR2086281B1 (enExample) |
| GB (1) | GB1343641A (enExample) |
| NL (1) | NL7105479A (enExample) |
| SU (1) | SU448654A3 (enExample) |
| ZA (1) | ZA712627B (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE786726A (fr) * | 1971-07-27 | 1973-01-26 | Ciba Geigy | Composes azoiques, leur procede d'obtention et leur emploi comme matieres colorantes |
| JP2013504647A (ja) * | 2009-09-11 | 2013-02-07 | フジフィルム・イメイジング・カラランツ・リミテッド | 染料およびインクジェット印刷におけるそれらの使用 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE947215C (de) * | 1952-01-30 | 1956-08-09 | Ciba Geigy | Verfahren zum Echtfaerben von anodisch oxydiertem Aluminium |
| DE1023161B (de) * | 1954-03-26 | 1958-01-23 | Cfmc | Verfahren zur Herstellung von Monoazofarbstoffen und deren Metallkomplexverbindungen |
| FR1136430A (fr) * | 1954-09-28 | 1957-05-14 | Bayer Ag | Colorants monoazoïques métallifères et leur procédé de production |
| DE951524C (de) * | 1954-09-30 | 1956-10-31 | Bayer Ag | Verfahren zur Herstellung von Azofarbstoffen |
| DE960753C (de) * | 1955-08-17 | 1957-03-28 | Bayer Ag | Verfahren zur Herstellung metallhaltiger Monoazofarbstoffe |
| DE1058172B (de) * | 1955-11-04 | 1959-05-27 | Bayer Ag | Verfahren zur Herstellung metallhaltiger Monoazofarbstoffe |
| DE1100845B (de) * | 1956-06-01 | 1961-03-02 | Geigy Ag J R | Verfahren zur Herstellung von metallisierbaren Azofarbstoffen und ihren Schwermetallkomplex-verbindungen |
| DE1085987B (de) * | 1958-01-23 | 1960-07-28 | Bayer Ag | Verfahren zur Herstellung metallhaltiger Monoazofarbstoffe |
| FR1211082A (fr) * | 1958-10-02 | 1960-03-14 | Cfmc | Nouveaux colorants azoïques basiques. application à la teinture des fibres acryliquues |
| CH493519A (de) * | 1965-04-29 | 1970-07-15 | Geigy Ag J R | Verfahren zur Herstellung von 2,3-Pyridindiol |
| CH471782A (de) * | 1966-08-31 | 1969-04-30 | Geigy Ag J R | Verfahren zur Herstellung eines neuen, substituierten 2,3-Pyridindiols |
| CH480410A (de) * | 1967-01-09 | 1969-10-31 | Geigy Ag J R | Verfahren zur Herstellung von wasserlöslichen Azopyrimidinfarbstoffen |
| CH502415A (de) * | 1968-07-02 | 1971-01-31 | Cassella Farbwerke Mainkur Ag | Verfahren zur Herstellung wasserlöslicher Azofarbstoffe |
-
1970
- 1970-04-23 CH CH607170A patent/CH561757A5/xx not_active IP Right Cessation
-
1971
- 1971-04-19 DE DE2118945A patent/DE2118945C2/de not_active Expired
- 1971-04-20 CS CS2849A patent/CS176156B2/cs unknown
- 1971-04-22 NL NL7105479A patent/NL7105479A/xx not_active Application Discontinuation
- 1971-04-22 GB GB1082271*[A patent/GB1343641A/en not_active Expired
- 1971-04-22 FR FR7114403A patent/FR2086281B1/fr not_active Expired
- 1971-04-22 DD DD154605A patent/DD96245A5/xx unknown
- 1971-04-22 AT AT347071A patent/AT304720B/de not_active IP Right Cessation
- 1971-04-23 BR BR2444/71A patent/BR7102444D0/pt unknown
- 1971-04-23 CA CA111,149A patent/CA970773A/en not_active Expired
- 1971-04-23 SU SU1649124A patent/SU448654A3/ru active
- 1971-04-23 BE BE766181A patent/BE766181A/xx unknown
- 1971-04-23 ZA ZA712627A patent/ZA712627B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2118945A1 (de) | 1971-11-04 |
| AT304720B (de) | 1973-01-25 |
| FR2086281B1 (enExample) | 1974-04-26 |
| DE2118945C2 (de) | 1982-12-02 |
| ZA712627B (en) | 1972-01-26 |
| BR7102444D0 (pt) | 1973-05-24 |
| CH561757A5 (enExample) | 1975-05-15 |
| FR2086281A1 (enExample) | 1971-12-31 |
| GB1343641A (en) | 1974-01-16 |
| CA970773A (en) | 1975-07-08 |
| NL7105479A (enExample) | 1971-10-26 |
| DD96245A5 (enExample) | 1973-03-12 |
| BE766181A (fr) | 1971-10-25 |
| CS176156B2 (enExample) | 1977-06-30 |
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