GB920390A - Shaped materials containing coloured copolymers - Google Patents
Shaped materials containing coloured copolymersInfo
- Publication number
- GB920390A GB920390A GB1696361A GB1696361A GB920390A GB 920390 A GB920390 A GB 920390A GB 1696361 A GB1696361 A GB 1696361A GB 1696361 A GB1696361 A GB 1696361A GB 920390 A GB920390 A GB 920390A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acryloylamino
- coupling product
- diazotized
- vinyl
- butyl acrylate
- 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
- 229920001577 copolymer Polymers 0.000 title abstract 3
- 239000000463 material Substances 0.000 title abstract 2
- 230000008878 coupling Effects 0.000 abstract 6
- 238000010168 coupling process Methods 0.000 abstract 6
- 238000005859 coupling reaction Methods 0.000 abstract 6
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 abstract 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 abstract 2
- LBSXSAXOLABXMF-UHFFFAOYSA-N 4-Vinylaniline Chemical compound NC1=CC=C(C=C)C=C1 LBSXSAXOLABXMF-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 238000012662 bulk polymerization Methods 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- WNVPACYPJUPHON-UHFFFAOYSA-N n-(4-aminophenyl)prop-2-enamide Chemical compound NC1=CC=C(NC(=O)C=C)C=C1 WNVPACYPJUPHON-UHFFFAOYSA-N 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 abstract 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- HGWQOFDAUWCQDA-UHFFFAOYSA-N 4-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(O)=CC=C(S(O)(=O)=O)C2=C1 HGWQOFDAUWCQDA-UHFFFAOYSA-N 0.000 abstract 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- ZVHNRPZXUCYKCU-UHFFFAOYSA-N N-(3-acetyl-4-amino-9,10-dioxoanthracen-1-yl)prop-2-enamide Chemical compound NC1=C(C=C(C=2C(C3=CC=CC=C3C(C12)=O)=O)NC(C=C)=O)C(C)=O ZVHNRPZXUCYKCU-UHFFFAOYSA-N 0.000 abstract 1
- SLADURSJMUIBEG-UHFFFAOYSA-N N-[9,10-dioxo-4-(prop-2-enoylamino)anthracen-1-yl]benzamide Chemical compound C(C=C)(=O)NC1=CC=C(C=2C(C3=CC=CC=C3C(C12)=O)=O)NC(C1=CC=CC=C1)=O SLADURSJMUIBEG-UHFFFAOYSA-N 0.000 abstract 1
- DWDZEJQBVCZSEW-UHFFFAOYSA-N N-[9,10-dioxo-5-(prop-2-enoylamino)anthracen-1-yl]benzamide Chemical compound C(C=C)(=O)NC1=CC=CC=2C(C3=C(C=CC=C3C(C12)=O)NC(C1=CC=CC=C1)=O)=O DWDZEJQBVCZSEW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004159 Potassium persulphate Substances 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- 229950011260 betanaphthol Drugs 0.000 abstract 1
- OTXQUGSUXRBUTC-UHFFFAOYSA-N butan-1-ol;toluene Chemical compound CCCCO.CC1=CC=CC=C1 OTXQUGSUXRBUTC-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 abstract 1
- 239000012969 di-tertiary-butyl peroxide Substances 0.000 abstract 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 abstract 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 abstract 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 abstract 1
- 150000002689 maleic acids Chemical class 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical group 0.000 abstract 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical class C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 abstract 1
- HFGXCYUIVSCHDN-UHFFFAOYSA-N n-(4-amino-2,5-dimethoxyphenyl)prop-2-enamide Chemical compound COC1=CC(NC(=O)C=C)=C(OC)C=C1N HFGXCYUIVSCHDN-UHFFFAOYSA-N 0.000 abstract 1
- YFIHOXAQIJAIHN-UHFFFAOYSA-N n-(4-phenyldiazenylphenyl)prop-2-enamide Chemical compound C1=CC(NC(=O)C=C)=CC=C1N=NC1=CC=CC=C1 YFIHOXAQIJAIHN-UHFFFAOYSA-N 0.000 abstract 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 abstract 1
- 235000019394 potassium persulphate Nutrition 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- -1 vinylidene halides Chemical class 0.000 abstract 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
- 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
- D06P1/0056—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres
- D06P1/006—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres by using dyes with polymerisable groups, e.g. dye ---CH=CH2
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/62—Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Structural Engineering (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB57856A DE1184949B (de) | 1960-05-14 | 1960-05-14 | Herstellung von transparentfarbigen Formkoerpern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB920390A true GB920390A (en) | 1963-03-06 |
Family
ID=6971859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1696361A Expired GB920390A (en) | 1960-05-14 | 1961-05-10 | Shaped materials containing coloured copolymers |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE603733A (enrdf_load_stackoverflow) |
| CH (2) | CH479644A (enrdf_load_stackoverflow) |
| DE (1) | DE1184949B (enrdf_load_stackoverflow) |
| FR (1) | FR1291903A (enrdf_load_stackoverflow) |
| GB (1) | GB920390A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3536440A (en) * | 1966-06-03 | 1970-10-27 | Bayer Ag | Process for the dyeing and printing of fibre substrates |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL287281A (enrdf_load_stackoverflow) * | 1961-12-29 | |||
| FR2280672A1 (fr) * | 1974-08-02 | 1976-02-27 | Ugine Kuhlmann | Copolymeres structurellement colores a base de colorants cyanovinyl-azoiques |
-
0
- BE BE603733D patent/BE603733A/xx unknown
-
1960
- 1960-05-14 DE DEB57856A patent/DE1184949B/de active Pending
-
1961
- 1961-05-05 CH CH530761A patent/CH479644A/de not_active IP Right Cessation
- 1961-05-05 CH CH997961A patent/CH380697A/de unknown
- 1961-05-10 GB GB1696361A patent/GB920390A/en not_active Expired
- 1961-05-13 FR FR861859A patent/FR1291903A/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3536440A (en) * | 1966-06-03 | 1970-10-27 | Bayer Ag | Process for the dyeing and printing of fibre substrates |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1184949B (de) | 1965-01-07 |
| CH380697A (de) | 1964-10-15 |
| BE603733A (enrdf_load_stackoverflow) | |
| FR1291903A (fr) | 1962-04-27 |
| CH997961A4 (enrdf_load_stackoverflow) | 1964-04-30 |
| CH479644A (de) | 1969-10-15 |
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