CH677857B5 - - Google Patents
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- Publication number
- CH677857B5 CH677857B5 CH2314/87A CH231487A CH677857B5 CH 677857 B5 CH677857 B5 CH 677857B5 CH 2314/87 A CH2314/87 A CH 2314/87A CH 231487 A CH231487 A CH 231487A CH 677857 B5 CH677857 B5 CH 677857B5
- Authority
- CH
- Switzerland
- Prior art keywords
- diallylamine
- group
- brookfield
- treatment
- base
- Prior art date
Links
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical class C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 claims abstract description 17
- 238000004043 dyeing Methods 0.000 claims abstract description 15
- 239000003999 initiator Substances 0.000 claims abstract description 14
- 229920000642 polymer Polymers 0.000 claims abstract description 12
- 239000004753 textile Substances 0.000 claims abstract description 11
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000178 monomer Substances 0.000 claims abstract description 6
- 125000000129 anionic group Chemical group 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 229920001519 homopolymer Polymers 0.000 claims description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 229920000768 polyamine Polymers 0.000 claims description 12
- 239000000975 dye Substances 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 239000000985 reactive dye Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 4
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 239000000982 direct dye Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 125000005001 aminoaryl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims description 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 2
- 125000002944 cyanoaryl group Chemical group 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 150000005690 diesters Chemical class 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 150000007522 mineralic acids Chemical class 0.000 claims 2
- 150000007524 organic acids Chemical class 0.000 claims 2
- 235000005985 organic acids Nutrition 0.000 claims 2
- 239000000758 substrate Substances 0.000 abstract description 5
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 229920006158 high molecular weight polymer Polymers 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 11
- 239000002585 base Substances 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000003929 acidic solution Substances 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000012458 free base Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000004045 reactive dyeing Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- LQCMNQDXLKGVLG-UHFFFAOYSA-N 1-propan-2-yl-4,5-dihydroimidazole;dihydrochloride Chemical compound Cl.Cl.CC(C)N1CCN=C1 LQCMNQDXLKGVLG-UHFFFAOYSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- RQGIHCLAHKOPPG-UHFFFAOYSA-N 2-methylbutanimidamide;dihydrochloride Chemical compound Cl.Cl.CCC(C)C(N)=N RQGIHCLAHKOPPG-UHFFFAOYSA-N 0.000 description 1
- XCENPWBBAXQVCG-UHFFFAOYSA-N 4-phenylpiperidine-4-carbaldehyde Chemical compound C=1C=CC=CC=1C1(C=O)CCNCC1 XCENPWBBAXQVCG-UHFFFAOYSA-N 0.000 description 1
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- ZTIBRLIVTVWLDO-UHFFFAOYSA-N Cl.Cl.CN(C(=N)CCC)C Chemical compound Cl.Cl.CN(C(=N)CCC)C ZTIBRLIVTVWLDO-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- -1 dial-lyl compound Chemical class 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 238000009967 direct dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- KJPUOJVUFLEJRP-UHFFFAOYSA-N n-[(4,6-dichloro-1,3,5-triazin-2-yl)methyl]-6-(naphthalen-2-yldiazenyl)naphthalen-2-amine Chemical compound ClC1=NC(Cl)=NC(CNC=2C=C3C=CC(=CC3=CC=2)N=NC=2C=C3C=CC=CC3=CC=2)=N1 KJPUOJVUFLEJRP-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- 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
- C08F126/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F126/02—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
- C08F126/04—Diallylamine
-
- 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
- D06P1/52—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 synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/5214—Polymers of unsaturated compounds containing no COOH groups or functional derivatives thereof
- D06P1/5242—Polymers of unsaturated N-containing compounds
-
- 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
- D06P5/08—After-treatment with organic compounds macromolecular
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerization Catalysts (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3622122 | 1986-07-02 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CH677857GA3 CH677857GA3 (en:Method) | 1991-07-15 |
| CH677857B5 true CH677857B5 (en:Method) | 1992-01-15 |
Family
ID=6304184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH2314/87A CH677857B5 (en:Method) | 1986-07-02 | 1987-06-19 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4864007A (en:Method) |
| JP (1) | JPS6323911A (en:Method) |
| CH (1) | CH677857B5 (en:Method) |
| FR (1) | FR2601022B1 (en:Method) |
| GB (1) | GB2192893B (en:Method) |
| IT (1) | IT1216828B (en:Method) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3706176A1 (de) * | 1987-02-26 | 1988-09-08 | Sandoz Ag | Mischung mit synergistischen eigenschaften |
| JPH0627137B2 (ja) * | 1989-09-22 | 1994-04-13 | 第一工業製薬株式会社 | ジアリルアミン及びその誘導体の重合方法 |
| EP0447352B1 (de) * | 1990-03-15 | 1994-12-21 | Ciba-Geigy Ag | Verfahren zur Verbesserung der Ausbeute und der Nassechtheiten von mit anionischen Farbstoffen auf Cellulosefasermaterial erzeugten Färbungen oder Drucken |
| US5382324A (en) * | 1993-05-27 | 1995-01-17 | Henkel Corporation | Method for enhancing paper strength |
| US5512636A (en) * | 1994-09-06 | 1996-04-30 | Betz Laboratories, Inc. | Cationic graft polymer agglomeration agents for mineral bearing ores |
| DE19509982A1 (de) * | 1995-03-18 | 1996-09-19 | Sandoz Ag | Textilnachbehandlungsmittel |
| GB9703814D0 (en) * | 1997-02-24 | 1997-04-16 | Ici Plc | Dyeing of textiles |
| WO2000024791A1 (en) | 1998-10-28 | 2000-05-04 | Penn State Research Foundation | Process for polymerization of allylic compounds |
| JP4631137B2 (ja) * | 2000-08-01 | 2011-02-16 | 日東紡績株式会社 | 末端にメルカプト基を有するアリルアミン類重合体およびその製造方法 |
| KR101762469B1 (ko) * | 2010-04-19 | 2017-07-27 | 니토 보세키 가부시기가이샤 | 디알릴아민 아세트산염 중합체의 제조 방법 |
| RU2439086C1 (ru) * | 2010-05-13 | 2012-01-10 | Государственное образовательное учреждение высшего профессионального образования Кабардино-Балкарский государственный университет им. Х.М. Бербекова | Поли-n, n-диаллиламиноэтановая кислота |
| KR101608226B1 (ko) | 2014-11-20 | 2016-04-14 | 주식회사 아모텍 | 감전보호소자 및 이를 구비한 휴대용 전자장치 |
| CN111205381A (zh) * | 2020-03-16 | 2020-05-29 | 中山市天信助剂实业有限公司 | 用于印染行业提高色牢度的环保型固色剂的制备方法 |
| GB2623090A (en) * | 2022-10-04 | 2024-04-10 | Sublino Ltd | Method of colouring |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3288770A (en) * | 1962-12-14 | 1966-11-29 | Peninsular Chem Res Inc | Water soluble quaternary ammonium polymers |
| JPS5618611A (en) * | 1979-07-24 | 1981-02-21 | Nippon Kayaku Co Ltd | Production of diallyldialkylammonium chloride |
| DE2946550A1 (de) * | 1979-11-17 | 1981-05-27 | Agfa-Gevaert Ag, 5090 Leverkusen | Polymere und verfahren zu ihrer herstellung |
| US4504640A (en) * | 1982-05-19 | 1985-03-12 | Nitto Boseki Co., Ltd. | Process for producing monoallylamine polymer |
| JPS6088018A (ja) * | 1983-10-21 | 1985-05-17 | Nitto Boseki Co Ltd | モノアリルアミンとジアリルアミン誘導体との共重合体の製造方法 |
| JPS60110987A (ja) * | 1983-11-15 | 1985-06-17 | 日東紡績株式会社 | 染色堅牢度向上法 |
| JPS61130318A (ja) * | 1984-11-29 | 1986-06-18 | Sumitomo Chem Co Ltd | ジアリルアミン重合体、その製法およびそれを含有する染色堅牢度向上剤 |
| JPS61231283A (ja) * | 1985-04-01 | 1986-10-15 | 日東紡績株式会社 | 染色堅牢度向上法 |
-
1987
- 1987-06-19 CH CH2314/87A patent/CH677857B5/de unknown
- 1987-06-25 IT IT8748099A patent/IT1216828B/it active
- 1987-06-26 FR FR878709112A patent/FR2601022B1/fr not_active Expired - Lifetime
- 1987-06-29 GB GB8715215A patent/GB2192893B/en not_active Expired - Lifetime
- 1987-06-30 US US07/068,462 patent/US4864007A/en not_active Expired - Fee Related
- 1987-07-01 JP JP62162516A patent/JPS6323911A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR2601022A1 (fr) | 1988-01-08 |
| GB2192893B (en) | 1990-07-04 |
| GB2192893A (en) | 1988-01-27 |
| US4864007A (en) | 1989-09-05 |
| FR2601022B1 (fr) | 1990-05-25 |
| IT8748099A0 (it) | 1987-06-25 |
| JPS6323911A (ja) | 1988-02-01 |
| CH677857GA3 (en:Method) | 1991-07-15 |
| GB8715215D0 (en) | 1987-08-05 |
| IT1216828B (it) | 1990-03-14 |
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