DE2400923A1 - Verfahren zur herstellung von dispersionen in organischen fluessigkeiten - Google Patents
Verfahren zur herstellung von dispersionen in organischen fluessigkeitenInfo
- Publication number
- DE2400923A1 DE2400923A1 DE19742400923 DE2400923A DE2400923A1 DE 2400923 A1 DE2400923 A1 DE 2400923A1 DE 19742400923 DE19742400923 DE 19742400923 DE 2400923 A DE2400923 A DE 2400923A DE 2400923 A1 DE2400923 A1 DE 2400923A1
- Authority
- DE
- Germany
- Prior art keywords
- parts
- weight
- tert
- dispersions
- meth
- 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.)
- Pending
Links
- 239000006185 dispersion Substances 0.000 title claims description 28
- 239000007788 liquid Substances 0.000 title claims description 10
- 238000002360 preparation method Methods 0.000 title claims description 7
- 238000000034 method Methods 0.000 title claims description 5
- 230000008569 process Effects 0.000 title claims description 4
- 229920000642 polymer Polymers 0.000 claims description 21
- 229920001577 copolymer Polymers 0.000 claims description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 9
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 8
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 229920003180 amino resin Polymers 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 229920001187 thermosetting polymer Polymers 0.000 claims 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 description 14
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 4
- 229920002521 macromolecule Polymers 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method 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
- 239000002904 solvent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- -1 hydroxypropyl Chemical group 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical compound CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- VOXYRZQCFVVAOZ-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.CC(O)COC(C)COC(C)CO VOXYRZQCFVVAOZ-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- 241000592335 Agathis australis Species 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KFKPWTFHOVSSSI-UHFFFAOYSA-N butyl 2-hydroxyprop-2-enoate Chemical compound CCCCOC(=O)C(O)=C KFKPWTFHOVSSSI-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- MSYLJRIXVZCQHW-UHFFFAOYSA-N formaldehyde;6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound O=C.NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 MSYLJRIXVZCQHW-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- JTRJYFZORBIJMZ-UHFFFAOYSA-N n-hexyl-n-octyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCC)CCCCCCCC JTRJYFZORBIJMZ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000008096 xylene 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
- C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
Landscapes
- 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)
- Paints Or Removers (AREA)
- Polymerisation Methods In General (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT90173A AT320279B (de) | 1973-02-01 | 1973-02-01 | Verfahren zur Herstellung von Dispersionen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2400923A1 true DE2400923A1 (de) | 1974-08-22 |
Family
ID=3502444
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19742400923 Pending DE2400923A1 (de) | 1973-02-01 | 1974-01-09 | Verfahren zur herstellung von dispersionen in organischen fluessigkeiten |
Country Status (10)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4764447A (en) * | 1985-07-17 | 1988-08-16 | Ricoh Co., Ltd. | Non-aqueous type resin dispersion and electrophotographic developer containing said resin |
| CA1335908C (en) * | 1988-10-07 | 1995-06-13 | Junji Oshima | Core-shell polymer, composition containing the polymers and its molded articles. |
| US5496905A (en) * | 1995-03-10 | 1996-03-05 | The Goodyear Tire & Rubber Company | Paint resin for use in paraffinic solvents |
| DE10010417C1 (de) * | 2000-03-03 | 2001-09-27 | Basf Coatings Ag | Wäßrige Sprühdosenlacke |
| US11440985B2 (en) * | 2017-01-19 | 2022-09-13 | Nissan Chemical Corporation | Underlayer film-forming composition for use in forming a microphase-separated pattern |
-
1973
- 1973-02-01 AT AT90173A patent/AT320279B/de active
-
1974
- 1974-01-04 IT IT1908774A patent/IT1006726B/it active
- 1974-01-09 DE DE19742400923 patent/DE2400923A1/de active Pending
- 1974-01-28 FR FR7402734A patent/FR2216303B3/fr not_active Expired
- 1974-01-29 PL PL16840774A patent/PL88578B1/pl unknown
- 1974-01-29 CS CS59974A patent/CS175471B2/cs unknown
- 1974-01-29 CA CA191,173A patent/CA1042582A/en not_active Expired
- 1974-01-31 GB GB461374A patent/GB1440282A/en not_active Expired
- 1974-02-01 JP JP1291474A patent/JPS49107391A/ja active Pending
- 1974-02-01 SU SU742000728A patent/SU629885A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| SU629885A3 (ru) | 1978-10-25 |
| PL88578B1 (enrdf_load_stackoverflow) | 1976-09-30 |
| CA1042582A (en) | 1978-11-14 |
| IT1006726B (it) | 1976-10-20 |
| GB1440282A (en) | 1976-06-23 |
| AT320279B (de) | 1975-02-10 |
| JPS49107391A (enrdf_load_stackoverflow) | 1974-10-11 |
| CS175471B2 (enrdf_load_stackoverflow) | 1977-05-31 |
| FR2216303A1 (enrdf_load_stackoverflow) | 1974-08-30 |
| FR2216303B3 (enrdf_load_stackoverflow) | 1976-11-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0506703B1 (de) | Lösliche vernetzbare copolymerisate auf der basis von vinylester-, vinylaromat- und acrylatmonomeren, verfahren zu ihrer herstellung sowie ihre verwendung in beschichtungsmitteln | |
| EP0363723B1 (de) | Verfahren zur Herstellung eines mehrschichtigen Überzuges, wässrige Beschichtungszusammensetzungen, wasserverdünnbare Polyacrylatharze und Verfahren zur Herstellung von wasserverdünnbaren Acrylatharzen | |
| DE3834638C2 (enrdf_load_stackoverflow) | ||
| DE3706095A1 (de) | Polysiloxan-haltiges harz und verfahren zu seiner herstellung | |
| DE2260211A1 (de) | Polymerisate, verfahren zu ihrer herstellung und ihre verwendung | |
| DE1520610A1 (de) | Polymerisate fuer hitzehaertbare UEberzugsmassen und Verfahren zu deren Herstellung | |
| EP0575931B1 (de) | In Zweistufenfahrweise hergestellte Vinylpolymerisate und ihre Verwendung als Lackbindemittel | |
| EP0995780B1 (de) | Wässrige, selbstvernetzende Copolymerisatdispersionen, ein Verfahren zu ihrer Herstellung und ihre Verwendung in Bindemitteln für Lacke | |
| DE2349154C2 (de) | Ein- oder mehrstufiges Verfahren zur Herstellung von Harzen | |
| DE2334084A1 (de) | Verfahren zur herstellung nichtwaesseriger polymerisatdispersionen | |
| DE68928225T2 (de) | Wässrige Anstrichzusammensetzung | |
| DE3913001A1 (de) | Hydroxylgruppenhaltiges bindemittel, verfahren zu dessen herstellung und seine verwendung | |
| DE3888774T2 (de) | Nichtwässrige Dispersion, Verfahren zu deren Herstellung und Anwendung. | |
| DE60127149T2 (de) | WÄSSRIGE DISPERSION von ADDITIONSPOLYMERTEILCHEN | |
| DE69509656T2 (de) | Katalytische zusammensetzungen und daraus hergestellte beschichtungen | |
| DE3622566C2 (enrdf_load_stackoverflow) | ||
| EP0416360B1 (de) | Sekundäre Aminogruppen aufweisende Copolymerisate, ein Verfahren zu ihrer Herstellung und ihre Verwendung als Bindemittel oder Bindemittelkomponente | |
| EP0655481A1 (de) | Wässrige Polymerdispersionen als Bindemittel für blockfeste, kratzfeste und chemikalienbeständige Beschichtungen | |
| DE2400923A1 (de) | Verfahren zur herstellung von dispersionen in organischen fluessigkeiten | |
| DE3779773T2 (de) | Verfahren zur herstellung einer dispersion von teilchen eines gelierten polymers. | |
| EP0022514A1 (de) | Wässrige Dispersion auf Grundlage von (Meth-)Acrylsäurederivaten, ihre Herstellung und Verwendung | |
| DE69004992T2 (de) | Selbstvernetzende wässrige Harzdispersion. | |
| WO1990015086A1 (de) | Carboxylgruppen und ggf. tertiäre aminogruppen enthaltende copolymere, verfahren zu ihrer herstellung und ihre verwendung in beschichtungsmassen | |
| DE3050850C2 (de) | Verfahren zur Herstellung einer wäßrigen Polymerdispersion | |
| DE69507402T2 (de) | Wässrige Polymerdispersionen für die Beschichtigung von Holz |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHW | Rejection |