FI112371B - Oksastettujen funktionalisoitujen polyorganosiloksaanien vesidispersiot, menetelmä niiden valmistamiseksi sekä niiden käyttö kovettuvien silikonikoostumusten valmistamiseen - Google Patents
Oksastettujen funktionalisoitujen polyorganosiloksaanien vesidispersiot, menetelmä niiden valmistamiseksi sekä niiden käyttö kovettuvien silikonikoostumusten valmistamiseen Download PDFInfo
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- FI112371B FI112371B FI943483A FI943483A FI112371B FI 112371 B FI112371 B FI 112371B FI 943483 A FI943483 A FI 943483A FI 943483 A FI943483 A FI 943483A FI 112371 B FI112371 B FI 112371B
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- FI
- Finland
- Prior art keywords
- grafted
- functionalized
- aqueous dispersions
- ethylenically unsaturated
- polyorganosiloxanes
- Prior art date
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- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
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- 238000004821 distillation Methods 0.000 description 2
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- 229920002545 silicone oil Polymers 0.000 description 2
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
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- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
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- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
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- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical group CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
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- 150000007513 acids Chemical class 0.000 description 1
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- 229910052783 alkali metal Inorganic materials 0.000 description 1
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- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
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- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
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- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
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- 235000019395 ammonium persulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
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- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000011230 binding agent Substances 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
- BVFSYZFXJYAPQJ-UHFFFAOYSA-N butyl(oxo)tin Chemical compound CCCC[Sn]=O BVFSYZFXJYAPQJ-UHFFFAOYSA-N 0.000 description 1
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- 239000011248 coating agent Substances 0.000 description 1
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- 229920005565 cyclic polymer Polymers 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
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- 229920005645 diorganopolysiloxane polymer Polymers 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000004213 low-fat Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
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- 238000002156 mixing Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005447 octyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 125000000466 oxiranyl 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 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
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
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- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
-
- 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
- C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
- C08F283/124—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes on to polysiloxanes having carbon-to-carbon double bonds
-
- 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
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
- C08F290/14—Polymers provided for in subclass C08G
- C08F290/148—Polysiloxanes
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/10—Block or graft copolymers containing polysiloxane sequences
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Silicon Polymers (AREA)
- Paints Or Removers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9309095 | 1993-07-23 | ||
| FR9309095A FR2707991B1 (fr) | 1993-07-23 | 1993-07-23 | Dispersions aqueuses de polyorganosiloxanes fonctionnalisés greffés, leur procédé de préparation et leur utilisation pour la réalisation de compositions silicones durcissables. |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI943483A0 FI943483A0 (fi) | 1994-07-22 |
| FI943483A FI943483A (fi) | 1995-01-24 |
| FI112371B true FI112371B (fi) | 2003-11-28 |
Family
ID=9449565
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI943483A FI112371B (fi) | 1993-07-23 | 1994-07-22 | Oksastettujen funktionalisoitujen polyorganosiloksaanien vesidispersiot, menetelmä niiden valmistamiseksi sekä niiden käyttö kovettuvien silikonikoostumusten valmistamiseen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5618879A (zh) |
| EP (2) | EP1273631B1 (zh) |
| CN (1) | CN1052244C (zh) |
| CA (1) | CA2128048C (zh) |
| DE (2) | DE69434629T2 (zh) |
| ES (1) | ES2254558T3 (zh) |
| FI (1) | FI112371B (zh) |
| FR (1) | FR2707991B1 (zh) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2729406B1 (fr) * | 1995-01-16 | 1997-04-18 | Rhone Poulenc Chimie | Utilisation a titre d'antiadherent et/ou d'hydrofugeant de polyorganosiloxanes fonctionnalises, greffes |
| US5973068A (en) * | 1996-11-07 | 1999-10-26 | Shin-Etsu Chemical Co., Ltd. | Silicone resin-containing emulsion composition, method for making same, and article having a cured film of same |
| JP3876946B2 (ja) * | 1998-01-20 | 2007-02-07 | 信越化学工業株式会社 | 帯電付与部材用コーティング剤及びそれを用いた電子写真用キャリア |
| FR2784115B1 (fr) | 1998-10-05 | 2000-12-15 | Rhodia Chimie Sa | Composition de revetements contenant des silicones fonctionnalisees |
| US6387997B1 (en) * | 1999-11-10 | 2002-05-14 | Ppg Industries Ohio, Inc. | Solvent-free film-forming compositions, coated substrates and method related thereto |
| DE10041163A1 (de) * | 2000-08-21 | 2002-03-07 | Basf Ag | Haarkosmetische Formulierungen |
| EP1713844B1 (de) * | 2004-03-11 | 2007-05-30 | Wacker Chemie AG | Verfahren zur herstellung von silikonhaltigen mischpolymerisaten |
| DE102004053314A1 (de) * | 2004-11-04 | 2006-05-11 | Wacker Chemie Ag | Verfahren zur Herstellung von mit Silikon modifizierten Polymerisaten |
| DE102005000824A1 (de) | 2005-01-05 | 2006-07-13 | Consortium für elektrochemische Industrie GmbH | Nanopartikelhaltige Organocopolymere |
| DE102005042752A1 (de) * | 2005-09-08 | 2007-03-15 | Wacker Chemie Ag | Hydrophile Silikonorganocopolymere |
| DE102006037270A1 (de) | 2006-08-09 | 2008-02-14 | Wacker Chemie Ag | Selbstdispergierbare Silikoncopolymerisate und Verfahren zu deren Herstellung und deren Verwendung |
| DE102006037271A1 (de) * | 2006-08-09 | 2008-02-14 | Wacker Chemie Ag | Vernetzbare reaktive Silikonorganocopolymere sowie Verfahren zu deren Herstellung und deren Verwendung |
| US20080085942A1 (en) * | 2006-10-05 | 2008-04-10 | Scott Jackson | Coating system, method of coating, and coated articles |
| DE102010062054A1 (de) | 2010-11-26 | 2012-05-31 | Wacker Chemie Ag | Wässriges Hybridbindemittel für Fugenmörtel |
| SG11201803293SA (en) * | 2015-10-22 | 2018-05-30 | Illumina Inc | Filler fluid for fluidic devices |
| DE102015223246A1 (de) * | 2015-11-24 | 2017-05-24 | Wacker Chemie Ag | Organocopolymer-Dispersionen |
| CN111212859B (zh) * | 2017-11-27 | 2023-06-06 | 三菱化学株式会社 | 含橡胶接枝聚合物、含有含橡胶接枝聚合物的树脂组合物及其成形体 |
| CN110396197B (zh) * | 2019-08-09 | 2024-07-23 | 雅思汀娜（北京）科技有限公司 | 一种硅油接枝聚合物以及一种疏水镀膜液及其制备方法和一种疏水膜 |
| EP4077485B1 (en) | 2019-12-18 | 2023-05-17 | Wacker Chemie AG | Crosslinkable reactive silicone organic copolymers dispersions |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3575910A (en) * | 1965-08-25 | 1971-04-20 | Dow Corning | Siloxane-acrylate copolymers and emulsions thereof |
| GB1149935A (en) * | 1966-10-14 | 1969-04-23 | Dow Corning | Siloxane-acrylate co-polymers, and emulsions thereof |
| IE892033L (en) * | 1988-07-07 | 1990-01-07 | Smc Patents Ltd | Aqueous emulsion copolymers with siloxane functionality |
| FR2644169B1 (zh) * | 1989-03-08 | 1991-05-24 | Thone Poulenc Chimie | |
| DE4119857A1 (de) * | 1991-06-17 | 1992-12-24 | Basf Lacke & Farben | Ueberzugsmittel auf der basis von carboxylgruppenhaltigen polymeren und epoxidharzen |
| DE69210542T2 (de) * | 1991-11-07 | 1996-10-31 | Takemoto Oil & Fat Co Ltd | Beschichtungsmittel |
-
1993
- 1993-07-23 FR FR9309095A patent/FR2707991B1/fr not_active Expired - Fee Related
-
1994
- 1994-07-08 EP EP02014319A patent/EP1273631B1/fr not_active Expired - Lifetime
- 1994-07-08 ES ES02014319T patent/ES2254558T3/es not_active Expired - Lifetime
- 1994-07-08 DE DE69434629T patent/DE69434629T2/de not_active Expired - Fee Related
- 1994-07-08 EP EP94420195A patent/EP0635526B1/fr not_active Expired - Lifetime
- 1994-07-08 DE DE69434035T patent/DE69434035T2/de not_active Expired - Fee Related
- 1994-07-14 CA CA002128048A patent/CA2128048C/fr not_active Expired - Fee Related
- 1994-07-22 CN CN94108005A patent/CN1052244C/zh not_active Expired - Fee Related
- 1994-07-22 FI FI943483A patent/FI112371B/fi active
-
1996
- 1996-03-25 US US08/621,320 patent/US5618879A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| FI943483A0 (fi) | 1994-07-22 |
| EP0635526B1 (fr) | 2004-09-29 |
| DE69434035T2 (de) | 2005-02-03 |
| EP1273631B1 (fr) | 2006-02-15 |
| DE69434629D1 (de) | 2006-04-20 |
| CA2128048C (fr) | 2000-05-23 |
| EP0635526A1 (fr) | 1995-01-25 |
| US5618879A (en) | 1997-04-08 |
| DE69434629T2 (de) | 2006-08-10 |
| CA2128048A1 (fr) | 1995-01-24 |
| FR2707991A1 (fr) | 1995-01-27 |
| DE69434035D1 (de) | 2004-11-04 |
| CN1103071A (zh) | 1995-05-31 |
| FI943483A (fi) | 1995-01-24 |
| ES2254558T3 (es) | 2006-06-16 |
| EP1273631A2 (fr) | 2003-01-08 |
| EP1273631A3 (fr) | 2003-08-06 |
| FR2707991B1 (fr) | 1995-09-15 |
| CN1052244C (zh) | 2000-05-10 |
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Legal Events
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| PC | Transfer of assignment of patent |
Owner name: BLUESTAR SILICONES FRANCE Free format text: BLUESTAR SILICONES FRANCE |