CN105377703A - 用于包装制品诸如食品和饮料容器的涂料组合物 - Google Patents
用于包装制品诸如食品和饮料容器的涂料组合物 Download PDFInfo
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- CN105377703A CN105377703A CN201480038126.6A CN201480038126A CN105377703A CN 105377703 A CN105377703 A CN 105377703A CN 201480038126 A CN201480038126 A CN 201480038126A CN 105377703 A CN105377703 A CN 105377703A
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- UYAAVKFHBMJOJZ-UHFFFAOYSA-N diimidazo[1,3-b:1',3'-e]pyrazine-5,10-dione Chemical compound O=C1C2=CN=CN2C(=O)C2=CN=CN12 UYAAVKFHBMJOJZ-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
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- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
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- NRZWYNLTFLDQQX-UHFFFAOYSA-N p-tert-Amylphenol Chemical compound CCC(C)(C)C1=CC=C(O)C=C1 NRZWYNLTFLDQQX-UHFFFAOYSA-N 0.000 description 1
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- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical class C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 229940116423 propylene glycol diacetate Drugs 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
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- 230000035939 shock Effects 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
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- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
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- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
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- 238000011105 stabilization Methods 0.000 description 1
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- 125000001036 sulfinic acid ester group Chemical group 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
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- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
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- 150000003752 zinc compounds Chemical class 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
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- B05D1/00—Processes for applying liquids or other fluent materials
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- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/28—Processes for applying liquids or other fluent materials performed by transfer from the surfaces of elements carrying the liquid or other fluent material, e.g. brushes, pads, rollers
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- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
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- B32B15/082—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising vinyl resins; comprising acrylic resins
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- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/085—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyolefins
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- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/095—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyurethanes
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- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/098—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising condensation resins of aldehydes, e.g. with phenols, ureas or melamines
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
- B65D25/14—Linings or internal coatings
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- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/02—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of acids, salts or anhydrides
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- 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
-
- 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
-
- 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
- C08F290/12—Polymers provided for in subclasses C08C or C08F
- C08F290/126—Polymers of unsaturated carboxylic acids or derivatives thereof
-
- 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
- C09D151/003—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 by reactions only involving unsaturated carbon-to-carbon 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
- 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
- C09D151/006—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 block copolymers containing at least one sequence of polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Mechanical Engineering (AREA)
- Dispersion Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Paints Or Removers (AREA)
- Details Of Rigid Or Semi-Rigid Containers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
Claims (54)
Priority Applications (1)
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CN201710699525.2A CN107541119B (zh) | 2013-07-02 | 2014-07-01 | 用于包装制品诸如食品和饮料容器的涂料组合物 |
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US201361842043P | 2013-07-02 | 2013-07-02 | |
US61/842,043 | 2013-07-02 | ||
PCT/US2014/045063 WO2015002958A1 (en) | 2013-07-02 | 2014-07-01 | Coating compositions for packaging articles such as food and beverage containers |
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CN201710699525.2A Division CN107541119B (zh) | 2013-07-02 | 2014-07-01 | 用于包装制品诸如食品和饮料容器的涂料组合物 |
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CN105377703A true CN105377703A (zh) | 2016-03-02 |
CN105377703B CN105377703B (zh) | 2017-09-08 |
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CN201710699525.2A Active CN107541119B (zh) | 2013-07-02 | 2014-07-01 | 用于包装制品诸如食品和饮料容器的涂料组合物 |
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US (2) | US10351714B2 (zh) |
EP (1) | EP3016868B1 (zh) |
CN (2) | CN105377703B (zh) |
PL (1) | PL3016868T3 (zh) |
WO (1) | WO2015002958A1 (zh) |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2060654A (en) * | 1979-09-29 | 1981-05-07 | Kansai Paint Co Ltd | Water-dispersed acrylic graft polymer coating composition |
WO1989001498A1 (en) * | 1987-08-13 | 1989-02-23 | The Valspar Corporation | Aqueous coating compositions |
CN1146996A (zh) * | 1995-07-24 | 1997-04-09 | 巴斯福公司 | 制备疏水改性的乳液聚合物和得到的聚合物及涂料组合物 |
Family Cites Families (79)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3297621A (en) | 1965-01-04 | 1967-01-10 | Archer Daniels Midland Co | Two step polymerization of tetrapolymer |
BE757936A (fr) | 1969-10-23 | 1971-04-01 | Bayer Ag | Procede de preparation de polymeres anioniques modifies en emulsion |
GB1421114A (en) | 1972-07-14 | 1976-01-14 | Canadian Ind | Thermosettable synthetic addition polymers |
US4198330A (en) | 1974-04-19 | 1980-04-15 | American Cyanamid Company | Polyurethane latices modified by a vinyl polymer |
US3991216A (en) | 1974-05-16 | 1976-11-09 | Ppg Industries, Inc. | Beverage containers coated with a water based liner |
CA1065988A (en) | 1974-05-16 | 1979-11-06 | Roger M. Christenson | Water-based liners for beverage containers |
GB1574721A (en) | 1976-03-03 | 1980-09-10 | Canadian Ind | Process for preparing aqueous copolymer emulsions |
US4148670A (en) | 1976-04-05 | 1979-04-10 | Amchem Products, Inc. | Coating solution for metal surface |
US4129712A (en) | 1976-08-17 | 1978-12-12 | M&T Chemicals Inc. | Interpolymers, method of preparing the same and emulsions thereof, and metal cans coated with the interpolymers |
CA1102465A (en) | 1976-08-26 | 1981-06-02 | Andreas Lindert | Protective coating for metal articles |
JPS567367Y2 (zh) | 1976-09-09 | 1981-02-18 | ||
JPS5339387A (en) | 1976-09-24 | 1978-04-11 | Nippon Jiyunyaku Kk | Method of making aquaous emulsion polymer |
US4151143A (en) | 1977-08-19 | 1979-04-24 | American Cyanamid Company | Surfactant-free polymer emulsion coating composition and method for preparing same |
NZ191816A (en) | 1978-10-24 | 1981-03-16 | Canadian Ind | Preparation of aqueous copolymer emulsion |
US4289674A (en) | 1978-11-29 | 1981-09-15 | Ppg Industries, Inc. | Base-solubilized acrylic polymers and aqueous resinous dispersions of acrylic polymers and epoxy resins |
US4289811A (en) | 1980-02-21 | 1981-09-15 | Celanese Corporation | Stable aqueous dispersions of mixed resins and process for use as coating compositions |
US4480058A (en) | 1980-12-04 | 1984-10-30 | Scm Corporation | Aqueous epoxy ester emulsions |
NZ205206A (en) | 1982-08-12 | 1986-07-11 | Scm Corp | Water-dispersed coating compositions containing alkylol acrylamide-containing copolymers |
US4499212A (en) | 1982-09-13 | 1985-02-12 | Scm Corporation | Thermosetting acrylic latexes |
US4567246A (en) | 1982-12-16 | 1986-01-28 | Celanese Corporation | Water-swellable crosslinked polymeric microgel particles and aqueous dispersions of organic film-forming resins containing the same |
US4547612A (en) | 1984-09-25 | 1985-10-15 | Mobil Oil Corporation | Production of lubricant and/or heavy distillate range hydrocarbons by light olefin upgrading |
US4487859A (en) | 1983-11-21 | 1984-12-11 | Scm Corporation | Self-curing water dispersed polymers |
US4503173A (en) | 1983-12-19 | 1985-03-05 | Scm Corporation | Self-curing water dispersed polymer blends |
DE3544337A1 (de) | 1985-12-14 | 1987-06-19 | Hoechst Ag | Polymerisatdispersionen, verfahren zu ihrer herstellung, sowie deren anwendung als bindemittel |
US4692491A (en) | 1985-12-30 | 1987-09-08 | Ppg Industries, Inc. | Polymer emulsion products |
US4647612A (en) | 1985-12-30 | 1987-03-03 | Ppg Industries, Inc. | Polymer emulsion products |
AU590104B2 (en) | 1986-08-20 | 1989-10-26 | Glidden Company, The | Thermosetting emulsion polymers |
GB8721538D0 (en) | 1987-09-14 | 1987-10-21 | Polyvinyl Chemie Holland Bv | Aqueous dispersions |
US4894397A (en) | 1988-04-21 | 1990-01-16 | S. C. Johnson & Son, Inc. | Stable emulsion polymers and methods of preparing same |
AU613550B2 (en) | 1989-01-17 | 1991-08-01 | Ppg Industries, Inc. | Use of mixed polymeric surfactants for improved properties |
US4948822A (en) | 1989-02-27 | 1990-08-14 | National Starch And Chemical Investment Holding Corporation | Laminating adhesives |
US4948834A (en) | 1989-03-27 | 1990-08-14 | Ppg Industries, Inc. | Vinyl chloride-olefin copolymers having good color stability and flexibility for container coatings |
JP2760102B2 (ja) | 1989-08-04 | 1998-05-28 | ジェイエスアール株式会社 | 金属コーティング用水性共重合体分散液およびその組成物 |
US5166272A (en) | 1990-04-02 | 1992-11-24 | Ppg Industries, Inc. | Emulsion polymers and coating compositions prepared therefrom |
US5244960A (en) | 1990-04-02 | 1993-09-14 | Ppg Industries, Inc. | Thermosetting waterborne coating compositions prepared from aqueous emulsion polymers |
US5173526A (en) | 1991-04-26 | 1992-12-22 | Air Products And Chemicals, Inc. | Aqueous polyurethane-vinyl polymer dispersions for coating applications |
DE4113839A1 (de) | 1991-04-27 | 1992-10-29 | Basf Ag | Verfahren zur herstellung einer emulgatorfreien polymerdispersion |
US5308890A (en) | 1993-02-26 | 1994-05-03 | Rohm And Haas Company | Emulsion polymer blend of a multi-stage latex and a non-film forming latex |
US5461125A (en) | 1993-04-30 | 1995-10-24 | Minnesota Mining And Manufacturing Company | Waterborne core-shell latex polymers |
US5714539A (en) | 1993-10-04 | 1998-02-03 | Ppg Industries, Inc. | Polymeric surfactant and latex made therefrom |
GB9408748D0 (en) | 1994-05-03 | 1994-06-22 | Zeneca Resins Bv | Production of aqueous polymer compositions |
GB9408725D0 (en) | 1994-05-03 | 1994-06-22 | Zeneca Resins Bv | Production of aqueous polymer compositions |
PL320422A1 (en) | 1994-11-29 | 1997-09-29 | Vianova Kunstharz Ag | Two-stage process of obtaining self-crosslinking copolymeric dispersions and their application in lacquers |
US5869590A (en) | 1995-04-12 | 1999-02-09 | Eastman Chemical Company | Waterborne polymers having pendant allyl groups |
EP0747442B1 (en) | 1995-06-07 | 2003-09-03 | National Starch and Chemical Investment Holding Corporation | Modified aqueous polyurethane dispersions and methods for making same |
JP4381510B2 (ja) | 1998-07-01 | 2009-12-09 | 三井化学株式会社 | 水性分散体組成物及びその製造方法 |
CA2283373A1 (en) | 1998-09-25 | 2000-03-25 | Akzo Nobel Nv | Aqueous cross-linkable polymer composition for use in coatings |
JP3159191B2 (ja) | 1998-12-09 | 2001-04-23 | 日本電気株式会社 | 半導体装置 |
GB9927432D0 (en) | 1999-11-20 | 2000-01-19 | Avecia Bv | Aqueous polymer emulsions |
GB0023514D0 (en) | 2000-09-26 | 2000-11-08 | Ici Plc | Aqueous dispersion of addition polymer particles |
JP2002155234A (ja) | 2000-11-24 | 2002-05-28 | Dainippon Ink & Chem Inc | 製缶塗料用水性樹脂組成物及びそれを用いた金属缶 |
US20020155235A1 (en) | 2001-02-13 | 2002-10-24 | Taylor James W. | Crosslinked coatings |
US6646041B2 (en) | 2001-09-25 | 2003-11-11 | Imperial Chemical Industries Plc | Aqueous dispersion of addition polymer particles |
US6683145B2 (en) | 2001-10-26 | 2004-01-27 | Basf Corporation | Hydrophobic lattices and coating compositions containing them |
US6872789B2 (en) | 2001-11-07 | 2005-03-29 | Akzo Nobel N.V. | Cross-linkable polymer composition |
US6762240B2 (en) | 2002-04-19 | 2004-07-13 | Ppg Industries Ohio, Inc. | Highly crosslinked polymer particles and coating compositions containing the same |
US7001952B2 (en) | 2002-04-19 | 2006-02-21 | Ppg Industries Ohio, Inc. | Coating compositions containing polyurethane dispersions and highly crosslinked polymer particles |
GB2397578B (en) | 2002-12-17 | 2004-12-08 | Ici Plc | Aqueous dispersions of polyurethane-addition polymer hybrid particles especially for use in coating compositions |
WO2004099261A1 (en) | 2003-05-06 | 2004-11-18 | Nuplex Resins B.V. | Emulsion polymerization process, polymer dispersion and film-forming composition |
US7241830B2 (en) | 2004-05-07 | 2007-07-10 | Ppg Industries Ohio, Inc. | Organic solvent-free film-forming compositions, multi-layer composite coatings, and related methods |
ATE376575T1 (de) | 2004-06-11 | 2007-11-15 | Nuplex Resins Bv | Mehrstufige wässrige polymerdispersion |
EP2420542B2 (en) | 2004-10-20 | 2018-09-19 | Valspar Sourcing, Inc. | Article and method of coating |
JP4682892B2 (ja) | 2005-04-19 | 2011-05-11 | セイコーエプソン株式会社 | マイクロカプセルの製造方法、マイクロカプセル、電気泳動表示装置および電子機器 |
US8281981B2 (en) | 2007-07-11 | 2012-10-09 | International Paper Company | Shipping and display container |
CN102256525B (zh) | 2008-12-16 | 2014-06-25 | 迪瓦西公司 | 地面涂饰施放器 |
WO2010097353A1 (en) | 2009-02-24 | 2010-09-02 | Akzo Nobel Coatings International B.V. | Latex emulsions and coating compositions formed from latex emulsions |
US9394456B2 (en) | 2009-02-24 | 2016-07-19 | Akzo Nobel Coatings International B.V. | Latex emulsions and coating compositions formed from latex emulsions |
BR112012001172B1 (pt) | 2009-07-17 | 2021-03-23 | Swimc Llc | Artigo, e, método |
EP2371870B1 (en) | 2010-04-01 | 2012-07-11 | Rohm and Haas Company | Multistage emulsion polymer and coatings formed therefrom |
US20120077030A1 (en) | 2010-09-23 | 2012-03-29 | Basf Se | Multistage preparation of aqueous pressure-sensitive adhesive dispersions for producing self-adhesive articles |
ES2529671T3 (es) | 2010-12-20 | 2015-02-24 | Dsm Ip Assets B.V. | Composición acuosa bio-renovable de polímero vinílico |
RU2615700C2 (ru) * | 2010-12-29 | 2017-04-06 | Акцо Нобель Коатингс Интернэшнл Б.В. | Латексные эмульсии и покрывающие композиции, образованные из латексных эмульсий |
WO2012109278A2 (en) | 2011-02-07 | 2012-08-16 | Valspar Sourcing, Inc. | Coating compositions for containers and other articles and methods of coating |
US20120302690A1 (en) | 2011-05-27 | 2012-11-29 | Ppg Industries Ohio, Inc. | Grafted acrylic comprising water soluble and water insoluble portions and lattices and coatings comprising the same |
EP2599844A1 (en) | 2011-12-02 | 2013-06-05 | PPG Industries Ohio Inc. | Coating composition for a food or beverage can |
EP2814746B1 (en) * | 2012-02-17 | 2019-09-18 | Swimc Llc | Methods and materials for the functionalization of polymers and coatings including functionalized polymer |
CA2912536C (en) | 2013-05-16 | 2021-12-14 | The Coca-Cola Company | Polymer compositions and coatings for food and beverage packaging |
EP3016868B1 (en) | 2013-07-02 | 2023-09-27 | Swimc Llc | Coating compositions for packaging articles such as food and beverage containers |
KR101884537B1 (ko) | 2013-07-02 | 2018-08-01 | 발스파 소싱 인코포레이티드 | 식품 및 음료 용기와 같은 패키징 물품을 위한 코팅 조성물 |
-
2014
- 2014-07-01 EP EP14741763.8A patent/EP3016868B1/en active Active
- 2014-07-01 PL PL14741763.8T patent/PL3016868T3/pl unknown
- 2014-07-01 US US14/902,501 patent/US10351714B2/en active Active
- 2014-07-01 CN CN201480038126.6A patent/CN105377703B/zh active Active
- 2014-07-01 CN CN201710699525.2A patent/CN107541119B/zh active Active
- 2014-07-01 WO PCT/US2014/045063 patent/WO2015002958A1/en active Application Filing
-
2019
- 2019-07-11 US US16/508,755 patent/US10829646B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2060654A (en) * | 1979-09-29 | 1981-05-07 | Kansai Paint Co Ltd | Water-dispersed acrylic graft polymer coating composition |
WO1989001498A1 (en) * | 1987-08-13 | 1989-02-23 | The Valspar Corporation | Aqueous coating compositions |
CN1146996A (zh) * | 1995-07-24 | 1997-04-09 | 巴斯福公司 | 制备疏水改性的乳液聚合物和得到的聚合物及涂料组合物 |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109219641A (zh) * | 2016-05-26 | 2019-01-15 | Ppg工业俄亥俄公司 | 涂覆有乳液聚合的胶乳聚合物的包装 |
CN113416458A (zh) * | 2016-05-26 | 2021-09-21 | Ppg工业俄亥俄公司 | 涂覆有乳液聚合的胶乳聚合物的包装 |
CN109790248A (zh) * | 2016-06-27 | 2019-05-21 | 华纳巴布科克绿色化学学院有限责任公司 | 无双酚a的交联聚合物组合物 |
CN109715739A (zh) * | 2016-07-15 | 2019-05-03 | Swimc有限公司 | 具有降低的风味剥落性质的胶乳涂料组合物 |
CN111247213A (zh) * | 2017-09-01 | 2020-06-05 | 宣伟投资管理有限公司 | 多级聚合物胶乳、含有该胶乳的涂料及其涂布的制品 |
TWI779096B (zh) * | 2018-09-14 | 2022-10-01 | 美國商Swimc有限公司 | 多級聚合物膠乳、含有該膠乳的塗料及其塗布的製品 |
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US10829646B2 (en) | 2020-11-10 |
CN107541119A (zh) | 2018-01-05 |
CN107541119B (zh) | 2020-12-04 |
US20160376446A1 (en) | 2016-12-29 |
PL3016868T3 (pl) | 2024-02-05 |
EP3016868A1 (en) | 2016-05-11 |
US10351714B2 (en) | 2019-07-16 |
US20190338144A1 (en) | 2019-11-07 |
CN105377703B (zh) | 2017-09-08 |
EP3016868B1 (en) | 2023-09-27 |
WO2015002958A1 (en) | 2015-01-08 |
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