BG61860B2 - Синтетичен полиамид с подобрени багрилни свойства - Google Patents

Синтетичен полиамид с подобрени багрилни свойства Download PDF

Info

Publication number: BG61860B2
Authority: BG; Bulgaria
Prior art keywords: compound; synthetic polyamide; synthetic; acid; compounds
Prior art date: 1989-01-21

Application number

BG098622A

Other languages

Bulgarian (bg)

English (en)

Inventor

Bansi Kaul

Angelos Vougioukas

Original Assignee

Clariant Finance /Bvi/ Limited

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.)

1989-01-21

Filing date

1994-02-28

Publication date

1998-07-31

1989-01-21 Priority claimed from DE3901717A external-priority patent/DE3901717A1/de

1989-01-21 Priority claimed from DE3901716A external-priority patent/DE3901716A1/de

1989-09-09 Priority claimed from DE3930089A external-priority patent/DE3930089A1/de

1994-02-28 Application filed by Clariant Finance /Bvi/ Limited filed Critical Clariant Finance /Bvi/ Limited

1998-07-31 Publication of BG61860B2 publication Critical patent/BG61860B2/bg

Links

239000004952 Polyamide Substances 0.000 title claims abstract description 29
229920002647 polyamide Polymers 0.000 title claims abstract description 29
238000004043 dyeing Methods 0.000 title claims abstract description 7
150000001875 compounds Chemical class 0.000 claims abstract description 25
238000000034 method Methods 0.000 claims description 6
125000003277 amino group Chemical group 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims 1
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 5
238000004040 coloring Methods 0.000 abstract description 2
239000000975 dye Substances 0.000 description 9
239000000835 fiber Substances 0.000 description 6
239000000985 reactive dye Substances 0.000 description 5
239000004744 fabric Substances 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000000980 acid dye Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
YNOSXQQLBPOTLB-UHFFFAOYSA-J [Na+].[Cr+3].Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N\c1ccccc1C([O-])=O.Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N/c1ccccc1C([O-])=O Chemical compound [Na+].[Cr+3].Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N\c1ccccc1C([O-])=O.Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N/c1ccccc1C([O-])=O YNOSXQQLBPOTLB-UHFFFAOYSA-J 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
UHXQPQCJDDSMCB-UHFFFAOYSA-L disodium;3-[[9,10-dioxo-4-(2,4,6-trimethyl-3-sulfonatoanilino)anthracen-1-yl]amino]-2,4,6-trimethylbenzenesulfonate Chemical compound [Na+].[Na+].CC1=CC(C)=C(S([O-])(=O)=O)C(C)=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=C(C)C=C(C)C(S([O-])(=O)=O)=C1C UHXQPQCJDDSMCB-UHFFFAOYSA-L 0.000 description 2
GYGVRMLIQVFLPE-UHFFFAOYSA-L disodium;3-[[n-ethyl-4-[[4-[(3-sulfonatophenyl)diazenyl]naphthalen-1-yl]diazenyl]anilino]methyl]benzenesulfonate Chemical compound [Na+].[Na+].C=1C=C(N=NC=2C3=CC=CC=C3C(N=NC=3C=C(C=CC=3)S([O-])(=O)=O)=CC=2)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 GYGVRMLIQVFLPE-UHFFFAOYSA-L 0.000 description 2
238000000605 extraction Methods 0.000 description 2
239000002657 fibrous material Substances 0.000 description 2
BTLSLHNLDQCWKS-UHFFFAOYSA-N oxocan-2-one Chemical compound O=C1CCCCCCO1 BTLSLHNLDQCWKS-UHFFFAOYSA-N 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000000843 powder Substances 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
RRETZLLHOMHNNB-UHFFFAOYSA-M sodium;1-amino-9,10-dioxo-4-(2,4,6-trimethylanilino)anthracene-2-sulfonate Chemical compound [Na+].CC1=CC(C)=CC(C)=C1NC1=CC(S([O-])(=O)=O)=C(N)C2=C1C(=O)C1=CC=CC=C1C2=O RRETZLLHOMHNNB-UHFFFAOYSA-M 0.000 description 2
AXMCIYLNKNGNOT-UHFFFAOYSA-N sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfophenyl)methyl]amino]phenyl]methyl]-n-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S(O)(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-N 0.000 description 2
238000009987 spinning Methods 0.000 description 2
YAXWOADCWUUUNX-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidine Chemical class CC1CCCN(C)C1(C)C YAXWOADCWUUUNX-UHFFFAOYSA-N 0.000 description 1
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
WFGMRESWHYSOKC-UHFFFAOYSA-N 1,3,3,4-tetramethylpiperazin-2-one Chemical compound CN1CCN(C)C(C)(C)C1=O WFGMRESWHYSOKC-UHFFFAOYSA-N 0.000 description 1
FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 1
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical class CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 1
QEPXACTUQNGGHW-UHFFFAOYSA-N 2,4,6-trichloro-1h-triazine Chemical compound ClN1NC(Cl)=CC(Cl)=N1 QEPXACTUQNGGHW-UHFFFAOYSA-N 0.000 description 1
JECOQZILBFQPFS-UHFFFAOYSA-N 2,4,6-trichlorothiazine Chemical compound ClN1SC(Cl)=CC(Cl)=C1 JECOQZILBFQPFS-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
VVMPKPRQECVYDV-UHFFFAOYSA-N 5-butyl-2-[[4-(4-butyl-2-sulfoanilino)-5,8-dihydroxy-9,10-dioxoanthracen-1-yl]amino]benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(CCCC)=CC=C1NC(C=1C(=O)C2=C(O)C=CC(O)=C2C(=O)C=11)=CC=C1NC1=CC=C(CCCC)C=C1S(O)(=O)=O VVMPKPRQECVYDV-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
229920002292 Nylon 6 Polymers 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
150000001844 chromium Chemical class 0.000 description 1
239000011651 chromium Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 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
125000001033 ether group Chemical group 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
159000000011 group IA salts Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical class OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 1
-1 hypophosphoric acid alkali salts Chemical class 0.000 description 1
125000001841 imino group Chemical group [H]N=* 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002074 melt spinning Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
229920000933 poly (ε-caprolactam) Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
239000012254 powdered material Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000000047 product Substances 0.000 description 1
QUBWRMVVDDDDBG-UHFFFAOYSA-M sodium;1-amino-4-(4-butylanilino)-9,10-dioxoanthracene-2-sulfonate Chemical compound [Na+].C1=CC(CCCC)=CC=C1NC1=CC(S([O-])(=O)=O)=C(N)C2=C1C(=O)C1=CC=CC=C1C2=O QUBWRMVVDDDDBG-UHFFFAOYSA-M 0.000 description 1
238000010186 staining Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
150000003585 thioureas Chemical class 0.000 description 1
125000004306 triazinyl group Chemical group 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- D06P5/02—After-treatment
- D06P5/04—After-treatment with organic compounds
- D06P5/06—After-treatment with organic compounds containing nitrogen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- 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
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/6426—Heterocyclic compounds

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Textile Engineering (AREA)
Engineering & Computer Science (AREA)
General Chemical & Material Sciences (AREA)
Polyamides (AREA)
Compositions Of Macromolecular Compounds (AREA)
Coloring (AREA)
Artificial Filaments (AREA)
Processes Of Treating Macromolecular Substances (AREA)

BG098622A 1989-01-21 1994-02-28 Синтетичен полиамид с подобрени багрилни свойства BG61860B2 (bg)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE3901717A DE3901717A1 (de)	1989-01-21	1989-01-21	Synthetische polyamide mit verbesserter anfaerbbarkeit
DE3901716A DE3901716A1 (de)	1989-01-21	1989-01-21	Synthetische polyamide mit verbesserter anfaerbbarkeit sowie in der masse gefaerbte synthetische polyamide
DE3930089A DE3930089A1 (de)	1989-09-09	1989-09-09	Modifizierte synthetische polyamide

Publications (1)

Publication Number	Publication Date
BG61860B2 true BG61860B2 (bg)	1998-07-31

Family

ID=27198948

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BG098622A BG61860B2 (bg)	1989-01-21	1994-02-28	Синтетичен полиамид с подобрени багрилни свойства

Country Status (10)

Country	Link
EP (2)	EP0618256B1 (tr)
JP (1)	JP3041819B2 (tr)
KR (1)	KR100199220B1 (tr)
BG (1)	BG61860B2 (tr)
BR (1)	BR9000241A (tr)
CZ (2)	CZ291961B6 (tr)
DE (2)	DE69032665T2 (tr)
ES (2)	ES2120545T3 (tr)
SK (1)	SK280042B6 (tr)
TR (1)	TR28862A (tr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4131926A1 (de) *	1990-10-04	1992-04-09	Sandoz Ag	Verfahren zum nachbehandeln von mit anionischen farbstoffen gefaerbten substraten
DE59502905D1 (de) *	1994-04-15	1998-08-27	Basf Ag	Inhärent licht- und hitzestabilisierte polyamide
GB9609742D0 (en) *	1996-05-10	1996-07-17	Clariant Int Ltd	Improvements in or relating to organic compounds
GB9800935D0 (en)	1998-01-17	1998-03-11	Clariant Int Ltd	Improvements in or relating to organic compounds
US6197060B1 (en)	1999-01-19	2001-03-06	Smith & Nephew, Inc.	Otologic prostheses
KR100450381B1 (ko) *	2002-04-09	2004-10-01	주식회사 효성	열, 자외선 안정성이 우수한 개질 폴리아미드6의 제조방법
CN1882739B (zh)	2003-11-19	2011-01-26	西巴特殊化学品控股有限公司	提高色泽深度的方法
KR101723700B1 (ko) *	2009-06-30	2017-04-18	바스프 에스이	착색가능한 입자를 포함하는 폴리아미드 섬유 및 그의 제조 방법
KR20180050646A (ko) *	2015-09-04	2018-05-15	디아이씨 가부시끼가이샤	안정제 화합물, 액정 조성물 및 표시 소자
CN107849458B (zh)	2015-09-04	2021-07-27	Dic株式会社	液晶组合物及使用其的液晶显示元件

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1469633A1 (de) *	1965-06-11	1969-04-30	Basf Ag	Verfahren zur Herstellung von Farbstoffmischungen
NL6509284A (tr) *	1965-07-17	1966-01-25
JPS5857444A (ja) *	1981-09-29	1983-04-05	Sumitomo Chem Co Ltd	安定化された合成樹脂組成物
DE3233951A1 (de) *	1982-09-14	1984-03-15	Chemische Werke Hüls AG, 4370 Marl	Carbonamidgruppenhaltige formmassen oder formkoerper mit verbesserter bestaendigkeit gegen die einwirkung von licht
DE3233953A1 (de) *	1982-09-14	1984-03-15	Chemische Werke Hüls AG, 4370 Marl	Carbonamidgruppenhaltige formmassen oder formkoerper mit verbesserter bestaendigkeit gegen die einwirkung von licht
US4847333A (en) *	1985-09-30	1989-07-11	The Boeing Company	Blended polyamide oligomers

1990
- 1990-01-17 EP EP94109533A patent/EP0618256B1/en not_active Expired - Lifetime
- 1990-01-17 EP EP90810040A patent/EP0379470B1/en not_active Expired - Lifetime
- 1990-01-17 DE DE69032665T patent/DE69032665T2/de not_active Expired - Fee Related
- 1990-01-17 DE DE69025963T patent/DE69025963T2/de not_active Expired - Fee Related
- 1990-01-17 ES ES94109533T patent/ES2120545T3/es not_active Expired - Lifetime
- 1990-01-17 ES ES90810040T patent/ES2087141T3/es not_active Expired - Lifetime
- 1990-01-20 KR KR1019900000737A patent/KR100199220B1/ko not_active Expired - Fee Related
- 1990-01-22 BR BR909000241A patent/BR9000241A/pt not_active IP Right Cessation
- 1990-01-22 CZ CZ1990307A patent/CZ291961B6/cs not_active IP Right Cessation
- 1990-01-22 SK SK307-90A patent/SK280042B6/sk unknown
- 1990-01-22 JP JP2010780A patent/JP3041819B2/ja not_active Expired - Fee Related
- 1990-01-22 TR TR00106/90A patent/TR28862A/tr unknown
1994
- 1994-02-28 BG BG098622A patent/BG61860B2/bg unknown
2002
- 2002-05-07 CZ CZ20021588A patent/CZ292091B6/cs not_active IP Right Cessation

Also Published As

Publication number	Publication date
EP0379470A2 (en)	1990-07-25
ES2120545T3 (es)	1998-11-01
EP0379470B1 (en)	1996-03-20
ES2087141T3 (es)	1996-07-16
HK1012654A1 (en)	1999-08-06
DE69025963D1 (de)	1996-04-25
JPH02265966A (ja)	1990-10-30
KR900011825A (ko)	1990-08-02
DE69025963T2 (de)	1996-11-21
SK30790A3 (en)	1999-07-12
BR9000241A (pt)	1990-11-20
EP0618256A2 (en)	1994-10-05
EP0618256B1 (en)	1998-09-16
DE69032665T2 (de)	1999-02-25
CZ292091B6 (cs)	2003-07-16
DE69032665D1 (de)	1998-10-22
KR100199220B1 (ko)	1999-06-15
CZ30790A3 (cs)	2000-08-16
JP3041819B2 (ja)	2000-05-15
EP0379470A3 (en)	1992-03-18
TR28862A (tr)	1997-09-23
SK280042B6 (sk)	1999-07-12
EP0618256A3 (en)	1995-04-26
CZ291961B6 (cs)	2003-06-18

Publication	Publication Date	Title
RU2061007C1 (ru)	1996-05-27	Способ получения солей анионных красителей
DE69602199T2 (de)	1999-11-11	Lichtstabilisiertes polyamid-substrat und verfahren zu seiner herstellung
EP0461206B1 (en)	1994-03-02	Synthetic polyamides and their salts
KR20070004054A (ko)	2007-01-05	염색성 폴리올레핀 섬유 및 직물
EP0379470B1 (en)	1996-03-20	Improved dyeability of synthetic polyamide
EP0897412B1 (en)	2003-12-17	Improvements in or relating to organic polyamide compounds
US6218452B1 (en)	2001-04-17	Dyeability or mass coloration of synthetic polyamide
JP4381377B2 (ja)	2009-12-09	Ｕｖルミネセンス化合物のポリマー材料への組み込み方法
US4263197A (en)	1981-04-21	Process for dyeing linear polyamides in the melt
DE3901717A1 (de)	1990-07-26	Synthetische polyamide mit verbesserter anfaerbbarkeit
RU2068903C1 (ru)	1996-11-10	Композиция для получения модифицированного полиамида
DE3932912A1 (de)	1991-04-11	Sterisch gehinderte aminogruppen enthaltende synthetische polyamide
KR20030065597A (ko)	2003-08-06	수성 매질에서 분산 염색용 안료 염료의 용도
DE4309436A1 (de)	1994-09-29	Sauer modifizierte synthetishe Polyamide
US3492266A (en)	1970-01-27	Polyamides stabilized with potassium or sodium cyanocuprates
DE3930089A1 (de)	1991-03-21	Modifizierte synthetische polyamide
JPS5833895B2 (ja)	1983-07-22	分散アントラキノン染料
DE2148512A1 (de)	1972-04-06	Neue Triazol-Derivate
DE3446284A1 (de)	1985-07-11	Faerbeverfahren
KR790000860B1 (ko)	1979-07-27	합성 선상 폴리아미드를 염색하는 방법
Zhun-zhui et al.	1987	Use of chemically dyed low-molecular polycaproamide to prepare dyed polypropylene yarn
WO2002079300A1 (en)	2002-10-10	Wetfast polyamide fiber with high amino end group content
DE2641043C3 (de)	1982-05-13	Massefärben von Polyamiden
DE3932914A1 (de)	1991-04-11	Aufhellersalze
EP0174793A2 (en)	1986-03-19	Perinone compound