DE10225652B4 - Seitenkettenmodifizierte Copolymerwachse - Google Patents
Seitenkettenmodifizierte Copolymerwachse Download PDFInfo
- Publication number
- DE10225652B4 DE10225652B4 DE10225652A DE10225652A DE10225652B4 DE 10225652 B4 DE10225652 B4 DE 10225652B4 DE 10225652 A DE10225652 A DE 10225652A DE 10225652 A DE10225652 A DE 10225652A DE 10225652 B4 DE10225652 B4 DE 10225652B4
- Authority
- DE
- Germany
- Prior art keywords
- acrylic acid
- chain
- side chain
- tetramethylpiperidinol
- long
- 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 - Fee Related
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 57
- 239000001993 wax Substances 0.000 title claims abstract description 39
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims abstract description 37
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 21
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 19
- 150000001336 alkenes Chemical class 0.000 claims abstract description 16
- 239000004711 α-olefin Substances 0.000 claims abstract description 13
- 125000005396 acrylic acid ester group Chemical group 0.000 claims abstract description 9
- 230000000269 nucleophilic effect Effects 0.000 claims abstract description 9
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 5
- 238000006243 chemical reaction Methods 0.000 claims abstract description 5
- 150000001412 amines Chemical class 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 19
- -1 perfluoroalkyl alcohols Chemical class 0.000 claims description 17
- 150000001298 alcohols Chemical class 0.000 claims description 14
- 239000003760 tallow Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 150000002191 fatty alcohols Chemical class 0.000 claims description 9
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims description 8
- 235000013162 Cocos nucifera Nutrition 0.000 claims description 8
- 244000060011 Cocos nucifera Species 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 8
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 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 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- UFCONGYNRWGVGH-UHFFFAOYSA-N 1-hydroxy-2,2,3,3-tetramethylpiperidine Chemical compound CC1(C)CCCN(O)C1(C)C UFCONGYNRWGVGH-UHFFFAOYSA-N 0.000 claims description 5
- VUZNLSBZRVZGIK-UHFFFAOYSA-N 2,2,6,6-Tetramethyl-1-piperidinol Chemical compound CC1(C)CCCC(C)(C)N1O VUZNLSBZRVZGIK-UHFFFAOYSA-N 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 claims description 5
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 claims description 4
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 4
- 239000004435 Oxo alcohol Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 claims description 4
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims description 4
- 239000004611 light stabiliser Substances 0.000 claims description 4
- GMTCPFCMAHMEMT-UHFFFAOYSA-N n-decyldecan-1-amine Chemical compound CCCCCCCCCCNCCCCCCCCCC GMTCPFCMAHMEMT-UHFFFAOYSA-N 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- UHVHCDKGRUZQBG-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethyl-1-oxidopiperidin-1-ium Chemical compound CC1(C)CCCC(C)(C)[N+]1(O)[O-] UHVHCDKGRUZQBG-UHFFFAOYSA-N 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 239000005871 repellent Substances 0.000 claims description 3
- 150000001414 amino alcohols Chemical class 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 239000006224 matting agent Substances 0.000 claims description 2
- 230000002940 repellent Effects 0.000 claims description 2
- 239000012748 slip agent Substances 0.000 claims description 2
- MTYYQFUGDQTTGX-UHFFFAOYSA-N 1-hydroxy-2,2,3,3-tetramethyl-1-oxidopiperidin-1-ium Chemical compound CC1(C([N+](CCC1)(O)[O-])(C)C)C MTYYQFUGDQTTGX-UHFFFAOYSA-N 0.000 claims 1
- 150000003926 acrylamides Chemical class 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 48
- 239000000203 mixture Substances 0.000 description 22
- 239000002253 acid Substances 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 12
- 239000000047 product Substances 0.000 description 9
- GVKORIDPEBYOFR-UHFFFAOYSA-K [butyl-bis(2-ethylhexanoyloxy)stannyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)O[Sn](CCCC)(OC(=O)C(CC)CCCC)OC(=O)C(CC)CCCC GVKORIDPEBYOFR-UHFFFAOYSA-K 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 5
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 238000013459 approach Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- SWZOQAGVRGQLDV-UHFFFAOYSA-N 4-[2-(4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)ethoxy]-4-oxobutanoic acid Chemical compound CC1(C)CC(O)CC(C)(C)N1CCOC(=O)CCC(O)=O SWZOQAGVRGQLDV-UHFFFAOYSA-N 0.000 description 1
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229920003247 engineering thermoplastic Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- AQYSYJUIMQTRMV-UHFFFAOYSA-N hypofluorous acid Chemical class FO AQYSYJUIMQTRMV-UHFFFAOYSA-N 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- AWGZKFQMWZYCHF-UHFFFAOYSA-N n-octylprop-2-enamide Chemical compound CCCCCCCCNC(=O)C=C AWGZKFQMWZYCHF-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- LCZVKKUAUWQDPX-UHFFFAOYSA-N tert-butyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]amino]ethyl]amino]acetate Chemical compound CC(=O)OC1=CC=CC=C1CN(CC(=O)OC(C)(C)C)CCN(CC(=O)OC(C)(C)C)CC1=CC=CC=C1OC(C)=O LCZVKKUAUWQDPX-UHFFFAOYSA-N 0.000 description 1
- OLBWDGJTEXRJLY-UHFFFAOYSA-N tetradecyl 3-(2,2,4,4-tetramethyl-21-oxo-7-oxa-3,20-diazadispiro[5.1.11^{8}.2^{6}]henicosan-20-yl)propanoate Chemical compound O1C2(CCCCCCCCCCC2)N(CCC(=O)OCCCCCCCCCCCCCC)C(=O)C21CC(C)(C)NC(C)(C)C2 OLBWDGJTEXRJLY-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/14—Esterification
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (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)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10225652A DE10225652B4 (de) | 2002-06-08 | 2002-06-08 | Seitenkettenmodifizierte Copolymerwachse |
| PCT/EP2003/005671 WO2003104289A1 (de) | 2002-06-08 | 2003-05-30 | Seitenkettenmodifizierte copolymerwachse |
| HK05111364.0A HK1079226B (en) | 2002-06-08 | 2003-05-30 | Side-chain-modified copolymer waxes |
| US10/516,929 US20060036013A1 (en) | 2002-06-08 | 2003-05-30 | Side-chain-modified copolymer waxes |
| JP2004511356A JP2005529204A (ja) | 2002-06-08 | 2003-05-30 | 側鎖変性されたコポリマーワックス |
| CNB03813165XA CN1284803C (zh) | 2002-06-08 | 2003-05-30 | 侧链改性的共聚物蜡 |
| EP03732502A EP1523507A1 (de) | 2002-06-08 | 2003-05-30 | Seitenkettenmodifizierte copolymerwachse |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10225652A DE10225652B4 (de) | 2002-06-08 | 2002-06-08 | Seitenkettenmodifizierte Copolymerwachse |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE10225652A1 DE10225652A1 (de) | 2003-12-24 |
| DE10225652B4 true DE10225652B4 (de) | 2004-10-28 |
Family
ID=29594350
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10225652A Expired - Fee Related DE10225652B4 (de) | 2002-06-08 | 2002-06-08 | Seitenkettenmodifizierte Copolymerwachse |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20060036013A1 (enExample) |
| EP (1) | EP1523507A1 (enExample) |
| JP (1) | JP2005529204A (enExample) |
| CN (1) | CN1284803C (enExample) |
| DE (1) | DE10225652B4 (enExample) |
| WO (1) | WO2003104289A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1681046A3 (de) * | 2004-11-13 | 2008-07-30 | Clariant Produkte (Deutschland) GmbH | Kosmetische, pharmazeutische und dermatologische Zubereitungen enthaltend Copolymerwachse |
| DE102005007980A1 (de) * | 2005-02-22 | 2006-02-23 | Clariant Gmbh | Kosmetische, pharmazeutische oder dermatologische Zubereitungen enthaltend Copolymerwachse |
| ES2340903A1 (es) * | 2008-09-22 | 2010-06-10 | Repsol Ypf, S.A. | Pelicula polimerica, procedimiento de obtencion y usos de la misma. |
| DE102009013902A1 (de) * | 2009-03-19 | 2010-09-23 | Clariant International Limited | Verwendung von Copolymerisaten als Additive für Lacke |
| DE102011014250A1 (de) * | 2011-03-17 | 2012-09-20 | Clariant International Ltd. | Pulverlackzusammensetzung zum Strukturieren und Texturieren von Lackoberflächen |
| CN115141547B (zh) * | 2022-06-01 | 2023-04-11 | 科顺防水科技股份有限公司 | 非固化防水涂料及其制备方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE590775A (enExample) * | 1959-05-15 | |||
| US4413096A (en) * | 1981-04-13 | 1983-11-01 | Ciba-Geigy Corporation | α-Olefin copolymers containing pendant hindered amine groups |
| CH669956A5 (enExample) * | 1985-07-13 | 1989-04-28 | Sandoz Ag | |
| US4885325A (en) * | 1985-07-13 | 1989-12-05 | Sandoz Ltd. | Water dispersible quaternized aminoamide-modified waxes useful as textile finishing agents |
| DE4139601C2 (de) * | 1991-11-30 | 1994-09-08 | Hoechst Ag | Copolymerisate und ihre Verwendung als Gleit- und Trennmittel für die Verarbeitung thermoplastischer Kunststoffe |
| DE60132318T2 (de) * | 2000-03-03 | 2009-01-08 | E.I. Du Pont De Nemours And Co., Wilmington | Verfahren zum vernetzen von ethylen-acrylester-polymeren |
| FR2826454B1 (fr) * | 2001-06-26 | 2003-10-17 | Bio Merieux | Cartes d'analyse |
-
2002
- 2002-06-08 DE DE10225652A patent/DE10225652B4/de not_active Expired - Fee Related
-
2003
- 2003-05-30 EP EP03732502A patent/EP1523507A1/de not_active Withdrawn
- 2003-05-30 JP JP2004511356A patent/JP2005529204A/ja not_active Withdrawn
- 2003-05-30 US US10/516,929 patent/US20060036013A1/en not_active Abandoned
- 2003-05-30 WO PCT/EP2003/005671 patent/WO2003104289A1/de not_active Ceased
- 2003-05-30 CN CNB03813165XA patent/CN1284803C/zh not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| Derwent-Abstract 1992-120228 der JP 04063880 * |
Also Published As
| Publication number | Publication date |
|---|---|
| HK1079226A1 (en) | 2006-03-31 |
| DE10225652A1 (de) | 2003-12-24 |
| US20060036013A1 (en) | 2006-02-16 |
| WO2003104289A1 (de) | 2003-12-18 |
| CN1284803C (zh) | 2006-11-15 |
| CN1659191A (zh) | 2005-08-24 |
| JP2005529204A (ja) | 2005-09-29 |
| EP1523507A1 (de) | 2005-04-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0941257B1 (de) | Polar modifizierte polypropylen-wachse | |
| EP0014746B1 (de) | Schmieröladditive | |
| EP0719290B1 (de) | Copolymerisate sowie deren reaktionsprodukte mit aminen als kraftstoff- und schmierstoffadditiv | |
| EP0036597B1 (de) | Schaumdämpfungsmittel und dessen Verwendung in Kunstharz-, Lack- und Farbdispersionen | |
| DE3339103A1 (de) | Additive fuer schmieroele | |
| WO1993022358A1 (de) | Copolymerisate aus carbonsäuren und quartären ammoniumverbindungen und ihre verwendung als verdickungs- oder dispergiermittel | |
| DE1136111B (de) | Verfahren zur Modifikation von butylkautschukartigen Mischpolymerisaten | |
| DE10225652B4 (de) | Seitenkettenmodifizierte Copolymerwachse | |
| EP0815150B1 (de) | Copolymerisate aus ungesättigten dicarbonsäuren oder deren anhydriden und vinylterminierten oligoolefinen sowie deren umsetzungsprodukte mit nucleophilen agentien | |
| DE4021095A1 (de) | Viskositaetsindex-verbesserer und verfahren zu seiner herstellung | |
| DE102009013902A1 (de) | Verwendung von Copolymerisaten als Additive für Lacke | |
| EP0447785B1 (de) | Polyacrylsäureester mit Ammoniumsalzgruppen | |
| EP2065411B1 (de) | Wachsartige Ionomere | |
| DE3017926A1 (de) | Fluoralkylacyloxysilane und deren verwendung | |
| EP2550318B1 (de) | Pe-wachsdispersionen bei der beschichtung von kunststoffen | |
| DE69224626T2 (de) | Zusammensetzungen und Verfahren zur Verbesserung des Schlupfes von Polyolefinen und der Adhäsion von auf Wasser basierenden Tinten auf Polyolefinen | |
| EP0028384B1 (de) | Oxidationsprodukte von Äthylen-Copolymerisaten und deren Verwendung | |
| WO2009033892A1 (de) | Verfahren zur beschichtung von oberflächen und dafür geeignete wässrige formulierungen | |
| EP2062925B1 (de) | Ionomere aus Poly-1-Olefinwachsen | |
| EP0201702A2 (de) | Wässrige Wachsdispersionen als Konservierungsmittel für Metall- und Lackoberflächen, ihre Verwendung und ein Verfahren zum Konservieren von Metall- und Lackoberflächen | |
| DE69319581T2 (de) | Verfahren zur Verbesserung des Bedruckens von Polyolefine mit wässrigen Druckfarbe | |
| JP2005529204A5 (enExample) | ||
| DE102009034914A1 (de) | Pigmentkonzentrate | |
| EP0931101A1 (de) | Neue polymer-in-polymer-dispersion als vi-verbesserer | |
| EP0358067B1 (de) | Vinylchloridcopolymerisate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OP8 | Request for examination as to paragraph 44 patent law | ||
| 8364 | No opposition during term of opposition | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: CLARIANT PRODUKTE (DEUTSCHLAND) GMBH, 65929 FRANKF |
|
| 8339 | Ceased/non-payment of the annual fee |