EP1711563A2 - Organosiliciumeinheiten enthaltende zubereitung auf acrylatbasis, deren herstellung und deren verwendung - Google Patents
Organosiliciumeinheiten enthaltende zubereitung auf acrylatbasis, deren herstellung und deren verwendungInfo
- Publication number
- EP1711563A2 EP1711563A2 EP04804783A EP04804783A EP1711563A2 EP 1711563 A2 EP1711563 A2 EP 1711563A2 EP 04804783 A EP04804783 A EP 04804783A EP 04804783 A EP04804783 A EP 04804783A EP 1711563 A2 EP1711563 A2 EP 1711563A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- preparation
- component
- acrylate
- optionally
- iii
- 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.)
- Ceased
Links
Classifications
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/442—Block-or graft-polymers containing polysiloxane sequences containing vinyl polymer sequences
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- 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
- C09D183/04—Polysiloxanes
- C09D183/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
-
- 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
-
- 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
Definitions
- the present invention relates to a special preparation containing acrylate-based organosilicon compounds, their preparation and their use.
- the substrate surface is usually pretreated, for example chemically by etching or by applying a primer.
- An aminoalkylalkoxysilane in water is often used as a primer.
- Organofunctional silanes and siloxanes are also used to modify the properties of
- a substrate surface can be created, for example, by a mechanical one
- EP 1 304 345 A2 discloses a mixture of aminoalkyl, alkoxy or hydroxy and optionally alkyl functional siloxanes which u. a. is used in paints and varnishes as a binder or adhesion promoter.
- the object of the present invention was to provide a further acrylate-based preparation containing organosilicon compounds.
- a particular concern was to create a radiation-curable, in To provide essential solvent-free printing ink for applications on plastic films.
- an acrylate-based preparation containing organosilicon compounds can advantageously be provided which, in addition to at least one acrylate,
- the present invention therefore relates to an acrylate-based preparation containing organosilicon compounds, the preparation in addition to at least one acrylate
- (v) optionally contains at least one reaction product of the present acrylate component with at least one component from the series (i), (ii) and (iii).
- Preparations according to the invention can thus contain at least one component (i) of the general formula I.
- groups R are identical or different and R represents a linear, cyclic, branched or substituted alkyl group, an alkoxy group or a hydroxyl group, groups R 'are identical or different and R' represents an alkoxy group or a hydroxy group, groups R "are the same or are different and R "stands for a silylaminoalkyl group bonded to a siloxane unit via Si-O-Si bond, x is 0 to ⁇ 2, y is> 0 to ⁇ 3, z is> 0 to ⁇ 3 and the Requirement (x + y + z) ⁇ 3, included.
- a preparation according to the invention also contains at least one component (ii) from the series 3- (4,5-dihydroimidazolyl) propyltrimethoxysilane and 3- (4,5-dihydroimidazolyl) propyltriethoxysilane or their reaction products.
- the starting materials or the components present in the preparation can also react with one another according to chemical understanding (also called reaction products here).
- the respective components present in the preparation can condense or co-condense, oligomerize, transesterify, hydrolyze, quilibrate, crosslink or follow a Michael addition - to name just a few examples.
- Preparations according to the invention can thus particularly preferably one component (iii) from the series of aminoalkylalkoxysilanes, for example, but not exclusively, 3-aminopropyltrialkoxysilanes, 3-aminopropylmethyldialkoxysilanes, N- (2-aminoethyl) -3-aminopropyltrialkoxysilanes, N- (2- Aminoethyl) -3- aminopropylmethyldialkoxysilane or corresponding reaction products of the aforementioned compounds contain, alkoxy here preferably being methoxy and ethoxy.
- Preparations according to the invention preferably also contain component (iv), the reaction products based on components (i), (ii) and / or (iii) having an average molar mass of 500 to 1,000 g / mol.
- a preparation according to the invention can contain a component (v), which is in particular the reaction product of a Michael addition based on component (ii) and the present acrylate component:
- X represents a further organic group and Y represents an organic radical, for example a silyl group, or the remainder of a reactive substrate surface, for example a corona-treated surface of a plastic film, or the remainder of a pigment present in the preparation, for example titanium dioxide.
- a preparation according to the invention contains an alcohol content of less than 5% by weight, and the present preparation is more advantageous Otherwise free of organic solvents.
- a present preparation preferably has a methanol, ethanol and / or isopropanol content of 1 ppm by weight to 3% by weight, particularly preferably 0.01 to 2% by weight.
- Preparations according to the invention preferably contain at least one acrylate from the urethane acrylate, functional acrylate, triacrylate and / or polyester acrylate base as the acrylate base.
- preparations according to the invention can contain a further content of color pigments, photoinitiators, UV absorbers - to name just a few examples - and / or further additives.
- the present invention furthermore relates to a process for the preparation of a preparation according to the invention, which is characterized in that an acrylate-containing starting composition, preferably an acrylate-containing lacquer or an acrylate-containing ink, in particular a printing ink, with components (i) and (ii) and, if appropriate brings together components (iii), (iv) and (v) and allows them to react with thorough mixing.
- an acrylate-containing starting composition preferably an acrylate-containing lacquer or an acrylate-containing ink, in particular a printing ink
- a mixture of aminoalkyl, alkoxy, optionally alkyl and optionally hydroxy-functional siloxanes is preferably used as component (i), at least one monomeric or oligomeric tetraalkoxysilane or (b) at least one for the preparation of this mixture Alkylalkoxysilane or (c) a mixture of at least one monomeric tetraalkoxysilane and / or an oligomeric tetraalkoxysilane and at least one alkylalkoxysilane, specifically hydrolyzed and precondensed by adding water and acid, and the siloxane-containing reaction mixture thus obtained adds at least one aminoalkyl-functional alkoxysilane (d), the Aminoalkylsilan condensed onto the siloxane units present in the reaction mixture and essentially enveloped, and alcohol removed from the system.
- oligomeric tetraethoxysilane is preferably used as compound (a).
- methyltrimethoxysilane, methyltriethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane or a mixture of at least two of the aforementioned alkoxysilanes is used as compound (b) in the preparation of component (i).
- Compounds (a) and (b) can also be used in a molar ratio of 1: 0 to 1: 1 as a mixture in the preparation of component (i) according to (c).
- An acid, in particular hydrogen chloride, is suitably used as the catalyst for the production of component (i).
- Aqueous hydrochloric acid preferably an approximately 37% hydrochloric acid, is preferably used in an amount of 60 to 100 ppm by weight, particularly preferably in an amount of 80 to 90 ppm by weight, in particular 84 ppm by weight, based on the amount of compounds (a) and (b) used.
- component (i) for hydrolysis and precondensation per mole of Si of components (a) and (b) preference is given in the preparation of component (i) for hydrolysis and precondensation per mole of Si of components (a) and (b) to a total of 0.7 to 1.6 moles, preferably 0.8 to 1.2, in particular preferably 0.85 to 1.0 mole of water.
- component (i) In the preparation of component (i), hydrolysis and precondensation of components (a) or (b) or (c) are carried out according to the invention in a solution diluted with alcohol.
- the reaction mixture suitably contains up to 60% by weight, preferably 20 to 45% by weight, of alcohol. Methanol or ethanol is preferably used.
- Hydrolysis and precondensation of the compounds (a) or (b) or (c) are preferably carried out in the preparation of component (i) under normal pressure at a temperature of 10 to 95 ° C., in particular over 2 to 3 hours at 70 to 80 ° C.
- At least one aminoalkyl-functional alkoxysilane is preferably added as compound (d) to component (i) in the preparation of component (i), compound (d) preferably being an aminoalkyl group from the series aminoethylamino propyl, aminoethylaminoethylamino propyl , N-methylaminopropyl, N- (n-butyl) aminopropyl, N-cyclohexylaminopropyl or N-phenylaminopropyl and at least one alkoxy group from the series methoxy, ethoxy or propoxy.
- the compounds (a), (b) and (d) are preferably used in a molar ratio of 1: 0: 1 to 1: 1: 1 in the preparation of component (i), ie. H.
- the molar ratio of components (a + b) to (d) is preferably 1: 1 to 2: 1.
- component (i) is carried out in such a way that the compound () after hydrolysis and precondensation of the compounds (a) or (b) or (c) at a temperature in the range from 30 to 100.degree. d) is added with thorough mixing, over a period of 5 minutes to 4 hours, in particular about 30 minutes at 70 to 80 ° C, suitably at a pH of 10 to 11, and then alcohol at a temperature in the range of 40 to 120 ° C, preferably from 80 to 90 ° C, removed from the system by distillation under normal pressure or under reduced pressure, so that (i) preferably contains less than 5% by weight of free alcohol.
- component (i) can also be produced according to the prior art and appropriate organosiloxanes used in the present process.
- EP 1 304 345 A2 discloses a mixture of aminoalkyl-alkoxy- or hydroxy- and optionally alkyl-functional siloxanes, which can suitably be used as component (i).
- EP 0 716 128 A2 disclose aqueous solutions of amino-functional organosilanes or organosiloxanes containing OH groups. These organosilane systems are practically completely hydrolyzed and the organofunctional silicon units are randomly distributed in the cocondensates and can also be used as amino-functional component (i) in the process according to the invention, taking into account the water content then present.
- Component (i) is suitably used in the process according to the invention with 0.05 to 15% by weight, preferably with 1 to 9% by weight, in particular with 3 to 7% by weight, based on the acrylate-containing preparation, for example one ready-to-use printing ink or an acrylic-based varnish.
- component (ii) in the present process preference is given to 3- (4,5- Dihydroimidazolyl) propyltriethoxysilane or 3- (4,5-dihydroimidazolyl) propyltriethoxysilane in an amount of 0.01 to 5% by weight, particularly preferably 0.1 to 3% by weight, in particular 0.5 to 1.5% by weight, based on the acrylate-containing preparation, ie, for example, a ready-to-use printing ink or an acrylate-based varnish.
- components (i) and (ii) together with component (iii) can be used in a weight ratio of 7: 1: 1 to 3: 0: 1, preferably 7: 0: 1 to 4: 1 : 1, particularly preferably from 5: 0: 1 to 5: 1: 1, where (iii) preferably from the series N- (2-aminoethyl) -3-aminopropyltrimethoxysilane, N- (2-aminoethyl) -3- aminopropyltriethoxysilane, N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, N- (2-aminoethyl) -3-aminopropylmethyldiethoxysilane, 3-
- components (i) and (ii) are preferably used in a weight ratio of 3: 0 to 7: 1.
- the product mixture obtained from components (i), (ii) and optionally (iii) is preferably added to an acrylate-containing composition with thorough mixing, according to the invention receives a ready-to-use, UV-curable preparation based on acrylate, which is particularly advantageous when applied due to excellent adhesive properties on substrate surfaces.
- the process according to the invention is carried out by first reacting component (i) by targeted hydrolysis and condensation of compounds (a) or (b) or (c) and then mixing the reaction products thus obtained with at least one compound in accordance with (d), if appropriate with further addition of water, can react.
- the reactions of the compounds (a) or (b) or (c) are suitably carried out in the presence of acid as a catalyst.
- acid as a catalyst.
- compound (d) is added, the pH in the reaction mixture generally rises to around 10 to 11.
- the reaction mixture is suitably allowed to react with thorough mixing and then alcohol can be at least partially removed from the system.
- component (i) is generally reacted with components (ii) and / or (iii) and, if appropriate, with the addition of auxiliary substances.
- the reactions described above can be carried out in suitable solvents or diluents. Alcohol formed during the reaction or solvents or diluents already present can be at least partially removed from the system after the reaction.
- the product mixture thus obtained is now mixed with an acrylate-based composition, in particular a lacquer or a printing ink, and is allowed to react, for example over about 30 to 60 minutes at room temperature.
- an acrylate-based composition in particular a lacquer or a printing ink
- the present acrylate-containing preparation can then be processed according to the invention.
- Preparations based on acrylate modified in this way are generally low-viscosity Systems and are characterized by excellent processability and excellent adhesive properties on the substrate surfaces treated with them.
- the present invention thus also relates to a preparation which can be obtained by the process according to the invention.
- the present invention furthermore relates to the use of a preparation according to the invention or one prepared or obtained according to the present method for the coating or labeling of natural substances, plastics, plastic foils, metal or metal foils.
- a preparation according to the invention is used for the coating of polyethylene (PE), polypropylene (PP), preferably oriented polypropylene (OPP), polyethylene terephthalate (PET), polyamide (PA), preferably oriented polyamide, aluminum or composite materials thereof, for example PPAM film (polypropylene / polyamide).
- a preparation according to the invention is used as a printing ink.
- a preparation according to the invention can be used particularly advantageously in the flexographic printing process.
- This printing process is part of the high pressure, whereby the elastic printing form (cliché) glued to a roller consists of parts that are to be printed, placed upside down, mirror-inverted parts and deeper lying, non-printing parts.
- the low-viscosity printing ink is brought from the ink tray onto the cliché by means of an anilox roller, which can take up different amounts of ink depending on the screening, and is transferred directly from this to the printing material.
- a preparation according to the invention for the production of a coating according to the flexographic printing process is therefore also an object.
- the coating of substrates with a preparation according to the invention can, however, also be carried out by means of customary paint application methods, such as painting, dipping, spraying, etc.
- Preparations according to the invention can advantageously be cured by irradiation.
- the coating is usually cured after the coating step.
- uniform curing of the present coating is advantageously achieved by UV curing under an inert gas.
- the use of a preparation according to the invention or such is also produced or obtained by the method according to the invention for a UV or electron beam crosslinking coating.
- Such coatings generally have excellent adhesion to one of the abovementioned substrates and usually have layer thicknesses of approximately ⁇ 100 ⁇ m, in particular from 0.5 to 80 ⁇ m, in particular from 1 to 50 ⁇ m.
- plastics, plastic films, metals, metal foils or composite materials made of metal and plastic which are advantageously provided with a coating according to the invention, are therefore also the subject of the present invention.
- the objects of the present invention include articles based on a material according to claim 34, for example — but not exclusively — plastics, plastic films, composite materials, etc.
- the present invention is illustrated by the following examples without restricting the scope.
- DYNASIL ® 40 submitted. The temperature is set to 70 ° C.
- Hydrochloric acid metered in with stirring.
- the reaction mixture is stirred for about 2 hours.
- 70 g of aminopropyltrimethoxysilane with a pH of 11 are added with stirring and a mixture of 5.5 g of water and 20 g of ethanol is added dropwise using a dropping funnel.
- the mixture is stirred at 75 to 80 ° C for a further 0.5 hour.
- Organosiloxane is a clear, colorless, low-viscosity liquid.
- the print sticks completely to the Tesa ® strip and, in comparison, does not show good adhesion to the PP film.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Paints Or Removers (AREA)
- Silicon Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE200410005824 DE102004005824A1 (de) | 2004-02-06 | 2004-02-06 | Organosiliciumeinheiten enthaltende Zubereitung auf Acrylatbasis, deren Herstellung und deren Verwendung |
PCT/EP2004/053419 WO2005075485A2 (de) | 2004-02-06 | 2004-12-13 | Organosiliciumeinheiten enthaltende zubereitung auf acrylatbasis, deren herstellung und deren verwendung |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1711563A2 true EP1711563A2 (de) | 2006-10-18 |
Family
ID=34801655
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP04804783A Ceased EP1711563A2 (de) | 2004-02-06 | 2004-12-13 | Organosiliciumeinheiten enthaltende zubereitung auf acrylatbasis, deren herstellung und deren verwendung |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1711563A2 (de) |
JP (1) | JP4773373B2 (de) |
CN (1) | CN1926201A (de) |
DE (1) | DE102004005824A1 (de) |
WO (1) | WO2005075485A2 (de) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3057576B1 (fr) * | 2016-10-14 | 2020-06-19 | Etablissements Tiflex | Nouvelle encre sol-gel destinee a l’impression par serigraphie |
CN106750318B (zh) * | 2016-12-08 | 2020-07-21 | 天津久日新材料股份有限公司 | 一种含有叔胺结构的聚硅氧烷丙烯酸酯及其制备方法和应用 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2621923A1 (fr) * | 1987-10-20 | 1989-04-21 | Rhone Poulenc Chimie | Composition organopolysiloxane a fonction cetiminoxy comportant un hydrogel comme agent de durcissement |
JP3226379B2 (ja) * | 1992-12-11 | 2001-11-05 | ポーラ化成工業株式会社 | ポリオルガノシロキサンおよびその製造方法 |
US5614324A (en) * | 1995-07-24 | 1997-03-25 | Gould Electronics Inc. | Multi-layer structures containing a silane adhesion promoting layer |
JP3895446B2 (ja) * | 1997-12-26 | 2007-03-22 | 株式会社ブリヂストン | 重合体の製造方法、得られた重合体、及びそれを用いたゴム組成物 |
JP2001131243A (ja) * | 1999-11-04 | 2001-05-15 | Shin Etsu Chem Co Ltd | 液状放射線硬化型樹脂組成物、光ファイバ用被覆材及び光ファイバ |
US7037953B2 (en) * | 2000-03-29 | 2006-05-02 | Sun Chemical Corporation | Radiation curable aqueous compositions |
DE10100384A1 (de) * | 2001-01-05 | 2002-07-11 | Degussa | Verfahren zur Modifizierung der Funktionalität von organofunktionellen Substratoberflächen |
DE10151264A1 (de) * | 2001-10-17 | 2003-04-30 | Degussa | Aminoalkylalkoxysiloxanhaltige Gemische, deren Herstellung und deren Verwendung |
JP2003157593A (ja) * | 2001-11-26 | 2003-05-30 | Dainippon Ink & Chem Inc | 紫外線硬化型組成物及びそれを用いた光ディスク |
-
2004
- 2004-02-06 DE DE200410005824 patent/DE102004005824A1/de not_active Withdrawn
- 2004-12-13 EP EP04804783A patent/EP1711563A2/de not_active Ceased
- 2004-12-13 CN CNA2004800426070A patent/CN1926201A/zh active Pending
- 2004-12-13 JP JP2006551740A patent/JP4773373B2/ja not_active Expired - Fee Related
- 2004-12-13 WO PCT/EP2004/053419 patent/WO2005075485A2/de active Application Filing
Non-Patent Citations (1)
Title |
---|
See references of WO2005075485A3 * |
Also Published As
Publication number | Publication date |
---|---|
JP4773373B2 (ja) | 2011-09-14 |
DE102004005824A1 (de) | 2005-08-25 |
JP2007520606A (ja) | 2007-07-26 |
WO2005075485A3 (de) | 2005-11-24 |
WO2005075485A2 (de) | 2005-08-18 |
CN1926201A (zh) | 2007-03-07 |
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