CH438738A - Verfahren zur Herstellung von stickstoffhaltigen Pfropfpolymerisaten - Google Patents
Verfahren zur Herstellung von stickstoffhaltigen PfropfpolymerisatenInfo
- Publication number
- CH438738A CH438738A CH2461A CH2461A CH438738A CH 438738 A CH438738 A CH 438738A CH 2461 A CH2461 A CH 2461A CH 2461 A CH2461 A CH 2461A CH 438738 A CH438738 A CH 438738A
- Authority
- CH
- Switzerland
- Prior art keywords
- polymer
- weight
- graft
- olefinically unsaturated
- polymers
- Prior art date
Links
- 229920000578 graft copolymer Polymers 0.000 title claims description 35
- 238000000034 method Methods 0.000 title claims description 23
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 title claims description 13
- 238000004519 manufacturing process Methods 0.000 title description 3
- 229920000642 polymer Polymers 0.000 claims description 54
- 239000000178 monomer Substances 0.000 claims description 43
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 22
- 239000004593 Epoxy Substances 0.000 claims description 17
- 239000004215 Carbon black (E152) Substances 0.000 claims description 16
- 229930195733 hydrocarbon Natural products 0.000 claims description 16
- 150000002430 hydrocarbons Chemical class 0.000 claims description 16
- 229920001223 polyethylene glycol Polymers 0.000 claims description 16
- 239000002202 Polyethylene glycol Substances 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 15
- 238000010559 graft polymerization reaction Methods 0.000 claims description 14
- 229920001451 polypropylene glycol Polymers 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 229920005601 base polymer Polymers 0.000 claims description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 5
- 150000002825 nitriles Chemical class 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000002685 polymerization catalyst Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- 230000007717 exclusion Effects 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- FCYVWWWTHPPJII-UHFFFAOYSA-N 2-methylidenepropanedinitrile Chemical compound N#CC(=C)C#N FCYVWWWTHPPJII-UHFFFAOYSA-N 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 description 28
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000000047 product Substances 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 9
- 150000003839 salts Chemical group 0.000 description 8
- 229920001519 homopolymer Polymers 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- -1 aliphatic alcohols Chemical class 0.000 description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 4
- 235000019400 benzoyl peroxide Nutrition 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 229920001515 polyalkylene glycol Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000001291 vacuum drying Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- GELKGHVAFRCJNA-UHFFFAOYSA-N 2,2-Dimethyloxirane Chemical compound CC1(C)CO1 GELKGHVAFRCJNA-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- LWQAYTWMEQUUFP-UHFFFAOYSA-K [K].I[Bi](I)I Chemical compound [K].I[Bi](I)I LWQAYTWMEQUUFP-UHFFFAOYSA-K 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002168 ethanoic acid esters Chemical class 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- RGBXDEHYFWDBKD-UHFFFAOYSA-N propan-2-yl propan-2-yloxy carbonate Chemical compound CC(C)OOC(=O)OC(C)C RGBXDEHYFWDBKD-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
- 238000010626 work up procedure Methods 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/06—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polyethers, polyoxymethylenes or polyacetals
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF30229A DE1111394B (de) | 1960-01-05 | 1960-01-05 | Verfahren zur Herstellung von Pfropfpolymerisaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH438738A true CH438738A (de) | 1967-06-30 |
Family
ID=37056983
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH2461A CH438738A (de) | 1960-01-05 | 1961-01-03 | Verfahren zur Herstellung von stickstoffhaltigen Pfropfpolymerisaten |
Country Status (7)
| Country | Link |
|---|---|
| BE (1) | BE598847A (enExample) |
| CH (1) | CH438738A (enExample) |
| DE (1) | DE1111394B (enExample) |
| FR (1) | FR1277220A (enExample) |
| GB (1) | GB969965A (enExample) |
| NL (1) | NL259615A (enExample) |
| SE (1) | SE305323B (enExample) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL269903A (enExample) * | 1960-10-04 | |||
| CA1077641A (en) * | 1974-08-28 | 1980-05-13 | Donald W. Simroth | Polymer/polyols and process for production thereof |
| US4494956A (en) * | 1982-12-14 | 1985-01-22 | Ciba-Geigy Corporation | Process for pad dyeing cellulosic textile materials |
| CA1318054C (en) * | 1988-10-03 | 1993-05-18 | Hans-Ulrich Berendt | Graft polymers which are water-soluble or dispersible in water, their preparation and use |
| EP0364399A3 (de) * | 1988-10-03 | 1992-04-29 | Ciba-Geigy Ag | Wasserlösliche oder in Wasser dispergierbare Mischpolymerisate, deren Herstellung und Verwendung |
| DE4440212A1 (de) * | 1994-11-10 | 1996-05-15 | Basf Schwarzheide Gmbh | Verfahren zur Herstellung von zelligen Polyurethanen |
| DE19526979A1 (de) | 1995-07-25 | 1997-01-30 | Basf Ag | Verfahren zur Herstellung von Hartschaumstoffen auf Isocyanatbasis |
| DE19528537A1 (de) | 1995-08-03 | 1997-02-06 | Basf Ag | Flammgeschützte Hartschaumstoffe auf Isocyanatbasis |
| JP4424995B2 (ja) | 2002-03-15 | 2010-03-03 | ビーエーエスエフ ソシエタス・ヨーロピア | 双峰の粒度分布を有するグラフトポリオール、このグラフトポリオールの製造、及びこのグラフトポリオールのポリウレタン製造のために使用する方法 |
| DE10226416A1 (de) * | 2002-06-13 | 2004-01-08 | Basf Ag | Polyoxyalkylen-substituierte Alkylendiamine und deren Verwendung in kosmetischen Formulierungen |
| DE102005063376B4 (de) | 2005-11-26 | 2018-10-11 | Tougas Oilfield Solutions Gmbh | Pfropfcopolymere und deren Verwendung |
| DE102007061883A1 (de) | 2007-12-20 | 2009-06-25 | Bayer Materialscience Ag | Viskoelastischer Polyurethanschaumstoff |
| DE102008000243A1 (de) | 2008-02-06 | 2009-08-13 | Evonik Goldschmidt Gmbh | Neuartige Kompatibilisierungsmittel zur Verbesserung der Lagerstabilität von Polyolmischungen |
| MX2011007402A (es) | 2009-01-12 | 2011-08-03 | Basf Se | Espumas de poliuretano flexibles, altamente elasticas. |
| EP2226344B1 (de) | 2009-03-02 | 2017-08-02 | Basf Se | Abriebbeständiger Polyurethanformkörper mit verbesserten Dauerbiegeeigenschaften |
| US8759411B2 (en) | 2010-02-01 | 2014-06-24 | Basf Se | Derivatives of diphosphines as flame retardants for polyurethanes |
| JP5814944B2 (ja) | 2010-02-01 | 2015-11-17 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | ポリウレタン用難燃剤としてのジホスフィン誘導体 |
| WO2011141266A1 (de) | 2010-04-15 | 2011-11-17 | Basf Se | Verfahren zur herstellung von flammgeschützten polyurethan-schaumstoffen |
| DE102011050220A1 (de) | 2011-05-09 | 2012-11-15 | Bayer Materialscience Aktiengesellschaft | Schwach modifizierte Präpolymere und ihre Anwendungen |
| CN103003323B (zh) | 2010-07-13 | 2016-03-02 | 拜耳知识产权有限责任公司 | 轻微改性的预聚物及其用途 |
| DE102010027052A1 (de) | 2010-07-13 | 2012-01-19 | Bayer Materialscience Ag | Verfahren zur Herstellung von isocyanatgruppenhaltigen Polyurethan-Präpolymeren |
| WO2012065299A1 (en) | 2010-11-16 | 2012-05-24 | Basf Se | Dimensionally stable low-density polyurethane moldings |
| US9062158B2 (en) | 2010-12-02 | 2015-06-23 | Basf Se | Polyester polyols based on aromatic dicarboxylic acids |
| EP2465657A1 (de) | 2010-12-16 | 2012-06-20 | Basf Se | Verfahren zur Herstellung niederdichter Polyurethanformkörper |
| EP2492297A1 (de) | 2011-02-23 | 2012-08-29 | Basf Se | Polyesterpolyole auf Basis aromatischer Dicarbonsäuren und daraus hergestellte Polyurethanhartschäume |
| EP2527381A1 (de) | 2011-05-26 | 2012-11-28 | Basf Se | Hochelastische Polyurethanschaumstoffe, enthaltend Ricinusöl |
| EP2602023A1 (de) | 2011-12-07 | 2013-06-12 | Basf Se | Katalysatorkombination zur Herstellung von Polyurethanschaumstoffformkörpern |
| BR112014017433A8 (pt) | 2012-01-18 | 2017-07-04 | Basf Se | processo para a produção de uma sola de sapato de poliuretano e sola de sapato de poliuretano |
| WO2013127647A1 (de) | 2012-03-01 | 2013-09-06 | Basf Se | Polyetheresterpolyole und ihre verwendung zur herstellung von polyurethan-hartschaumstoffen |
| EP2690118A1 (de) | 2012-07-27 | 2014-01-29 | Basf Se | Polyurethane enthaltend Phosphorverbindungen |
| EP2799459A1 (de) | 2013-05-03 | 2014-11-05 | Basf Se | Polyurethane enthaltend Halogenverbindungen |
| ES2704427T3 (es) | 2012-09-13 | 2019-03-18 | Basf Se | Poliuretanos que contienen compuestos de halógenos |
| EP2730596A1 (de) | 2012-11-13 | 2014-05-14 | Basf Se | Polyurethanweichschaumstoffe enthaltend Pflanzensamen |
| EP2746309A1 (de) | 2012-12-19 | 2014-06-25 | Basf Se | Hydrolysebeständige Polyurethanformkörper aus Polyesterpolyurethan |
| EP2818489A1 (de) | 2013-06-28 | 2014-12-31 | Basf Se | Hydrolysebeständige Polyurethanformkörper |
| CN105745243A (zh) | 2013-11-08 | 2016-07-06 | 巴斯夫欧洲公司 | 聚氨酯密封剂 |
| US20180086872A1 (en) | 2015-04-17 | 2018-03-29 | Basf Se | Polyurethanes with reduced aldehyde emission |
| CN109071758A (zh) | 2016-05-12 | 2018-12-21 | 巴斯夫欧洲公司 | 无粘性的聚氨酯软质泡沫 |
| EP3455271B1 (de) | 2016-05-12 | 2021-02-10 | Basf Se | Viskoelastische schaumstoffe mit hoher dichte |
| KR102436173B1 (ko) | 2016-06-15 | 2022-08-24 | 바스프 에스이 | 폴리올 중의 폴리아미드 분산액 및 이의 제법 |
| EP3649178A1 (de) | 2017-07-05 | 2020-05-13 | Basf Se | Schwefelhaltige polyesterpolyole, deren herstellung und verwendung |
| CN111093930B (zh) | 2017-09-13 | 2023-05-26 | 巴斯夫欧洲公司 | 经三轴压缩的拉胀的聚氨酯泡沫和三聚氰胺泡沫 |
| IL293877B2 (en) | 2019-12-17 | 2025-08-01 | Basf Se | A flexible foaming process for producing thermally insulated articles |
| WO2021229044A1 (en) | 2020-05-14 | 2021-11-18 | Basf Se | Electrically dissipative polyurethane foams and use thereof in trench breakers or pipeline pillows |
| WO2021259832A1 (en) | 2020-06-22 | 2021-12-30 | Basf Se | Viscoelastic elastomeric polyurethane foams, process for preparing them and use thereof |
| MX2023001018A (es) | 2020-07-24 | 2023-03-01 | Basf Se | Estructura multicapa y un proceso para preparar la misma. |
| WO2023036801A1 (en) | 2021-09-07 | 2023-03-16 | Basf Se | Ionic monomer- based polyurethane foams and use thereof in trench breakers or pipeline pillows or thermally insulative material |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1081230A (en) * | 1913-01-07 | 1913-12-09 | Howard Hunt Pen Company C | Pen-making machine. |
-
0
- NL NL259615D patent/NL259615A/xx unknown
- BE BE598847D patent/BE598847A/xx unknown
-
1960
- 1960-01-05 DE DEF30229A patent/DE1111394B/de active Pending
-
1961
- 1961-01-03 CH CH2461A patent/CH438738A/de unknown
- 1961-01-04 SE SE8761A patent/SE305323B/xx unknown
- 1961-01-05 FR FR848898A patent/FR1277220A/fr not_active Expired
- 1961-01-05 GB GB56761A patent/GB969965A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE1111394B (de) | 1961-07-20 |
| NL259615A (enExample) | |
| BE598847A (enExample) | |
| GB969965A (en) | 1964-09-16 |
| SE305323B (enExample) | 1968-10-21 |
| FR1277220A (fr) | 1961-11-24 |
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