CN107652786B - 涂料组合物 - Google Patents
涂料组合物 Download PDFInfo
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- CN107652786B CN107652786B CN201710970413.6A CN201710970413A CN107652786B CN 107652786 B CN107652786 B CN 107652786B CN 201710970413 A CN201710970413 A CN 201710970413A CN 107652786 B CN107652786 B CN 107652786B
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- 239000008199 coating composition Substances 0.000 title claims abstract description 161
- 239000006185 dispersion Substances 0.000 claims abstract description 84
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- 239000000203 mixture Substances 0.000 claims abstract description 59
- 239000002904 solvent Substances 0.000 claims abstract description 24
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- 229920000642 polymer Polymers 0.000 claims description 19
- 229920005601 base polymer Polymers 0.000 claims description 14
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 13
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- VATRWWPJWVCZTA-UHFFFAOYSA-N 3-oxo-n-[2-(trifluoromethyl)phenyl]butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1C(F)(F)F VATRWWPJWVCZTA-UHFFFAOYSA-N 0.000 claims description 3
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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
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- 239000002270 dispersing agent Substances 0.000 description 6
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- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 6
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- 238000006243 chemical reaction Methods 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
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- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 4
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 4
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
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- 125000002947 alkylene group Chemical group 0.000 description 4
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
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- 239000001257 hydrogen Substances 0.000 description 4
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- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 4
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- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
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- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
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- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
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- 229910000166 zirconium phosphate Inorganic materials 0.000 description 1
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 description 1
Classifications
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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
- C09D123/00—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers
- C09D123/02—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D123/10—Homopolymers or copolymers of propene
- C09D123/12—Polypropene
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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
- C09D123/00—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers
- C09D123/02—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D123/10—Homopolymers or copolymers of propene
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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
- 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
- C09D133/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
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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
- C09D151/003—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
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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
- C09D191/00—Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
- C09D191/06—Waxes
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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
- 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
- C09D5/024—Emulsion paints including aerosols characterised by the additives
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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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
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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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/65—Additives macromolecular
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- 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
- C08G77/445—Block-or graft-polymers containing polysiloxane sequences containing polyester sequences
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- 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
- C08G77/46—Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L2201/54—Aqueous solutions or dispersions
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/08—Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/06—Waxes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31692—Next to addition polymer from unsaturated monomers
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Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9169406B2 (en) * | 2003-08-25 | 2015-10-27 | Dow Global Technologies Llc | Coating compositions |
| EP3115428B1 (en) * | 2012-12-28 | 2019-08-28 | Dow Global Technologies LLC | A coating composition and articles made therefrom |
| WO2014105464A1 (en) * | 2012-12-28 | 2014-07-03 | Dow Global Technologies Llc | Coating compositions |
| US20170183506A1 (en) * | 2014-06-12 | 2017-06-29 | Dow Global Technologies Llc | Powder coatings |
| CN107207124B (zh) * | 2014-12-23 | 2020-04-21 | 智能包装有限公司 | 用于消费品的涂覆有含有白藜芦醇的层的容器 |
| WO2018119275A1 (en) | 2016-12-23 | 2018-06-28 | Saint-Gobain Abrasives, Inc. | Coated abrasives having a performance enhancing composition |
| US10808144B2 (en) | 2017-05-22 | 2020-10-20 | Ppg Industries Ohio, Inc. | Polyolefin silicon coating composition |
| JP7128659B2 (ja) * | 2017-06-15 | 2022-08-31 | ダウ グローバル テクノロジーズ エルエルシー | 機能性ポリオレフィンフィルムでコーティングされた紙 |
| MX2020002451A (es) | 2017-09-11 | 2020-07-20 | Honeywell Int Inc | Composiciones de pintura que incluyen formulaciones de copolimero para mejorar la adhesion a sustratos metalicos. |
| CN108250848A (zh) * | 2017-12-26 | 2018-07-06 | 重庆安特管业有限公司 | 一种管道浸塑工艺 |
| US11174409B2 (en) * | 2018-05-01 | 2021-11-16 | Dow Global Technologies Llc | Coated metal food container article |
| JP7419357B2 (ja) * | 2018-10-17 | 2024-01-22 | ダウ グローバル テクノロジーズ エルエルシー | コーティング組成物、コーティングされた布、コーティングされた布を作製する方法、およびコーティングされた布から作製された物品 |
| SG10201909497UA (en) * | 2018-10-22 | 2020-05-28 | Dow Global Technologies Llc | Coating compositions |
| KR102470778B1 (ko) * | 2018-12-17 | 2022-11-28 | 주식회사 엘지화학 | 열가소성 폴리에스테르 엘라스토머 수지 조성물, 이의 제조방법 및 이를 포함하는 성형품 |
| KR102538846B1 (ko) * | 2018-12-21 | 2023-06-01 | 주식회사 엘지화학 | 열가소성 폴리에스테르 엘라스토머 수지 조성물 및 이의 제조방법, 이를 포함하는 성형품 |
| US12031049B2 (en) | 2019-01-08 | 2024-07-09 | Kansai Paint Co., Ltd. | Aqueous coating material composition |
| KR20220099551A (ko) | 2019-11-14 | 2022-07-13 | 에스더블유아이엠씨 엘엘씨 | 금속 패키징 분말 코팅 조성물, 코팅된 금속 기재, 및 방법 |
| US20220411675A1 (en) | 2019-12-05 | 2022-12-29 | Mitsui Chemicals, Inc. | Aqueous dispersion and laminate |
| WO2021225764A1 (en) | 2020-05-05 | 2021-11-11 | Dow Global Technologies Llc | Paper coated with a functional polyolefin film |
| MX2022015653A (es) * | 2020-06-12 | 2023-01-16 | Swimc Llc | Composicion de revestimiento para recipientes para bebidas. |
| KR102230601B1 (ko) * | 2021-01-29 | 2021-03-22 | 최병선 | 수성티타늄 페인트 및 그 도장방법 |
| EP4341349A4 (en) | 2021-05-19 | 2025-07-16 | Swimc Llc | METHODS FOR COATING METAL SUBSTRATES AND MANUFACTURING METAL PACKAGING, COATED METAL SUBSTRATES, METAL PACKAGING AND POWDER COATING COMPOSITION SYSTEMS |
| CN114196289B (zh) * | 2021-12-27 | 2022-09-27 | 有沣(厦门)实业有限公司 | 一种喷涂用色漆及其制备工艺 |
| EP4655350A1 (en) * | 2023-01-26 | 2025-12-03 | PPG Industries Ohio Inc. | Wear resistant and lubricating coating composition for flexible substrates |
| CN116554596A (zh) * | 2023-04-28 | 2023-08-08 | 宁波东海塑料有限公司 | 一种抗油污的塑料油箱及其制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998002305A1 (en) * | 1996-07-15 | 1998-01-22 | Mobil Oil Corporation | Metallized multilayer packaging film |
| CN1651239A (zh) * | 2004-02-06 | 2005-08-10 | 株式会社神户制钢所 | 树脂涂布金属板及其制造方法 |
| CN102498043A (zh) * | 2009-07-24 | 2012-06-13 | 陶氏环球技术有限责任公司 | 涂布的容器装置、其制备方法 |
Family Cites Families (163)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4076698A (en) | 1956-03-01 | 1978-02-28 | E. I. Du Pont De Nemours And Company | Hydrocarbon interpolymer compositions |
| US3245934A (en) | 1960-12-19 | 1966-04-12 | Pennsalt Chemicals Corp | Production of finely divided polyolefin from preformed polymeric gel |
| US3422049A (en) | 1961-12-20 | 1969-01-14 | Nat Distillers Chem Corp | Process of preparing finely divided thermoplastic resins |
| US3746681A (en) | 1961-12-20 | 1973-07-17 | Nat Distillers Chem Corp | Process of preparing finely divided thermoplastic resins |
| US3166613A (en) | 1962-02-08 | 1965-01-19 | Eastman Kodak Co | Polyolefin powder process |
| US3900438A (en) * | 1964-03-20 | 1975-08-19 | Rohm & Haas | Copolymer-wax composition |
| US3432483A (en) | 1965-02-18 | 1969-03-11 | Nat Distillers Chem Corp | Continuous process for preparing finely divided polymers |
| US3456044A (en) | 1965-03-12 | 1969-07-15 | Heinz Erich Pahlke | Biaxial orientation |
| CA849081A (en) | 1967-03-02 | 1970-08-11 | Du Pont Of Canada Limited | PRODUCTION OF ETHYLENE/.alpha.-OLEFIN COPOLYMERS OF IMPROVED PHYSICAL PROPERTIES |
| US3554994A (en) | 1967-04-03 | 1971-01-12 | Standard Oil Co | Process for altering the particle size distribution of alpha monoolefin polymers |
| US3741253A (en) | 1971-03-30 | 1973-06-26 | Grace W R & Co | Laminates of ethylene vinyl acetate polymers and polymers of vinylidene chloride |
| US3908050A (en) | 1974-06-19 | 1975-09-23 | Continental Can Co | Metal coating compositions prepared from aqueous dispersions of carboxyl containing polyester resins |
| JPS5647208B2 (enExample) | 1974-11-29 | 1981-11-09 | ||
| US4352849A (en) | 1981-03-26 | 1982-10-05 | W. R. Grace & Co. | Coextruded, heat-shrinkable, multi-layer, polyolefin packaging film |
| US4597920A (en) | 1981-04-23 | 1986-07-01 | E. I. Du Pont De Nemours And Company | Shrink films of ethylene/α-olefin copolymers |
| DE3127133A1 (de) | 1981-07-09 | 1983-01-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von polyolefinen und deren copolymerisaten |
| US4543399A (en) | 1982-03-24 | 1985-09-24 | Union Carbide Corporation | Fluidized bed reaction systems |
| US4588790A (en) | 1982-03-24 | 1986-05-13 | Union Carbide Corporation | Method for fluidized bed polymerization |
| US5324800A (en) | 1983-06-06 | 1994-06-28 | Exxon Chemical Patents Inc. | Process and catalyst for polyolefin density and molecular weight control |
| US4599392A (en) | 1983-06-13 | 1986-07-08 | The Dow Chemical Company | Interpolymers of ethylene and unsaturated carboxylic acids |
| JPS60142076U (ja) | 1984-02-27 | 1985-09-20 | 関東自動車工業株式会社 | トルクレンチ |
| US4551380A (en) | 1984-05-10 | 1985-11-05 | W. R. Grace & Co., Cryovac Div. | Oriented heat-sealable multilayer packaging film |
| US4818785A (en) | 1985-04-16 | 1989-04-04 | Mitsui Petrochemical Industries, Ltd. | Fine particulate crosslinked amorphous copolymer and preparation and use thereof |
| US5059481A (en) | 1985-06-17 | 1991-10-22 | Viskase Corporation | Biaxially stretched, heat shrinkable VLDPE film |
| US4897455A (en) | 1985-06-21 | 1990-01-30 | Exxon Chemical Patents Inc. | Polymerization process |
| US4808561A (en) | 1985-06-21 | 1989-02-28 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
| US4689351A (en) | 1985-10-08 | 1987-08-25 | Mitsubishi Yuka Badische Co., Ltd. | Process for producing foamed particles of propylene copolymer resin |
| US4798081A (en) | 1985-11-27 | 1989-01-17 | The Dow Chemical Company | High temperature continuous viscometry coupled with analytic temperature rising elution fractionation for evaluating crystalline and semi-crystalline polymers |
| US4752597A (en) | 1985-12-12 | 1988-06-21 | Exxon Chemical Patents Inc. | New polymerization catalyst |
| US5008288A (en) | 1986-01-06 | 1991-04-16 | Alfred Stracher | Carnitine directed pharmaceutical agents |
| US4865902A (en) | 1986-01-17 | 1989-09-12 | E. I. Du Pont De Nemours And Company | Multilayered polyolefin high shrinkage, low-shrink force shrink film |
| US4749616A (en) | 1986-06-20 | 1988-06-07 | Mobil Oil Corporation | Heat sealable aqueous latex coating composition for polymer film |
| US5198401A (en) | 1987-01-30 | 1993-03-30 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| PL276385A1 (en) | 1987-01-30 | 1989-07-24 | Exxon Chemical Patents Inc | Method for polymerization of olefines,diolefins and acetylene unsaturated compounds |
| IL85097A (en) | 1987-01-30 | 1992-02-16 | Exxon Chemical Patents Inc | Catalysts based on derivatives of a bis(cyclopentadienyl)group ivb metal compound,their preparation and their use in polymerization processes |
| US5391629A (en) | 1987-01-30 | 1995-02-21 | Exxon Chemical Patents Inc. | Block copolymers from ionic catalysts |
| CA1324749C (en) | 1987-04-10 | 1993-11-30 | Vincent Wayne Herran | Flexible stretch/shrink film |
| US4988781A (en) | 1989-02-27 | 1991-01-29 | The Dow Chemical Company | Process for producing homogeneous modified copolymers of ethylene/alpha-olefin carboxylic acids or esters |
| US4963419A (en) | 1987-05-13 | 1990-10-16 | Viskase Corporation | Multilayer film having improved heat sealing characteristics |
| US4837084A (en) | 1987-07-02 | 1989-06-06 | W. R. Grace & Co.-Conn. | Thermoplastic multi-layer packaging film and bags made therefrom |
| US4820557A (en) | 1987-09-17 | 1989-04-11 | W. R. Grace & Co.-Conn. | Thermoplastic packaging film of low I10 /I2 |
| US4912075A (en) | 1987-12-17 | 1990-03-27 | Exxon Chemical Patents Inc. | Method for preparing a supported metallocene-alumoxane catalyst for gas phase polymerization |
| US4937217A (en) | 1987-12-17 | 1990-06-26 | Exxon Chemical Patents Inc. | Method for utilizing triethylaluminum to prepare an alumoxane support for an active metallocene catalyst |
| US4937301A (en) | 1987-12-17 | 1990-06-26 | Exxon Chemical Patents Inc. | Method for preparing a supported metallocene-alumoxane catalyst for gas phase polymerization |
| US5120867A (en) | 1988-03-21 | 1992-06-09 | Welborn Jr Howard C | Silicon-bridged transition metal compounds |
| US5017714A (en) | 1988-03-21 | 1991-05-21 | Exxon Chemical Patents Inc. | Silicon-bridged transition metal compounds |
| US5086025A (en) | 1988-03-29 | 1992-02-04 | Exxon Chemical Patents Inc. | Method for preparing a silica gel supported metallocene-alumoxane catalyst |
| US5147949A (en) | 1988-03-29 | 1992-09-15 | Exxon Chemical Patents Inc. | Polymerization process using a silica gel supported metallocene-alumoxane catalyst |
| US4871705A (en) | 1988-06-16 | 1989-10-03 | Exxon Chemical Patents Inc. | Process for production of a high molecular weight ethylene a-olefin elastomer with a metallocene alumoxane catalyst |
| FR2634212B1 (fr) | 1988-07-15 | 1991-04-19 | Bp Chimie Sa | Appareillage et procede de polymerisation d'olefines en phase gazeuse dans un reacteur a lit fluidise |
| DE3830535A1 (de) | 1988-09-08 | 1990-03-22 | Basf Ag | Verfahren zur herstellung von waessrigen synthesewachsdispersionen |
| US4952451A (en) | 1988-11-17 | 1990-08-28 | W. R. Grace & Co.-Conn. | Stretch/shrink film with improved oxygen transmission |
| ATE137770T1 (de) | 1989-10-10 | 1996-05-15 | Fina Technology | Metallocenkatalysator mit lewissäure und alkylaluminium |
| US5763549A (en) | 1989-10-10 | 1998-06-09 | Fina Technology, Inc. | Cationic metallocene catalysts based on organoaluminum anions |
| ES2071086T5 (es) | 1989-10-30 | 2002-01-16 | Fina Technology | Preparacion de catalizadores metalocenicos para polimerizacion de olefina. |
| US5387568A (en) | 1989-10-30 | 1995-02-07 | Fina Technology, Inc. | Preparation of metallocene catalysts for polymerization of olefins |
| DE4005947A1 (de) | 1990-02-26 | 1991-08-29 | Basf Ag | Loesliche katalysatorsysteme zur polymerisation von c(pfeil abwaerts)2(pfeil abwaerts)- bis c(pfeil abwaerts)1(pfeil abwaerts)(pfeil abwaerts)0(pfeil abwaerts)-alk-1-enen |
| EP0551277B2 (en) | 1990-06-22 | 2005-03-09 | ExxonMobil Chemical Patents Inc. | Aluminum-free monocyclopentadienyl metallocene catalysts for olefin polymerization |
| US5272236A (en) | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
| US5243001A (en) | 1990-11-12 | 1993-09-07 | Hoechst Aktiengesellschaft | Process for the preparation of a high molecular weight olefin polymer |
| US5189192A (en) | 1991-01-16 | 1993-02-23 | The Dow Chemical Company | Process for preparing addition polymerization catalysts via metal center oxidation |
| US5272200A (en) | 1991-02-15 | 1993-12-21 | Kuraray Co., Ltd. | Aqueous dispersion and substrate coated with the same |
| FI924965L (fi) | 1991-03-04 | 1992-11-03 | Dow Chemical Co | Foerfarande foer foerbaettring av termooksidativ stabilitet av etenpolymerer |
| US5228531A (en) | 1991-06-14 | 1993-07-20 | Deere & Company | Battery hold-down mechanism |
| DE4120009A1 (de) | 1991-06-18 | 1992-12-24 | Basf Ag | Loesliche katalysatorsysteme zur herstellung von polyalk-1-enen mit hohen molmassen |
| US5721185A (en) | 1991-06-24 | 1998-02-24 | The Dow Chemical Company | Homogeneous olefin polymerization catalyst by abstraction with lewis acids |
| US5288531A (en) | 1991-08-09 | 1994-02-22 | The Dow Chemical Company | Pouch for packaging flowable materials |
| TW300901B (enExample) | 1991-08-26 | 1997-03-21 | Hoechst Ag | |
| US5847053A (en) | 1991-10-15 | 1998-12-08 | The Dow Chemical Company | Ethylene polymer film made from ethylene polymer blends |
| DE59210001D1 (de) | 1991-10-15 | 2005-02-17 | Basell Polyolefine Gmbh | Verfahren zur Herstellung eines Olefinpolymers unter Verwendung von Metallocenen mit speziell substituierten Indenylliganden |
| JPH05105791A (ja) | 1991-10-15 | 1993-04-27 | Mitsubishi Petrochem Co Ltd | プロピレン重合体水性分散液 |
| US5278272A (en) | 1991-10-15 | 1994-01-11 | The Dow Chemical Company | Elastic substantialy linear olefin polymers |
| US5677383A (en) | 1991-10-15 | 1997-10-14 | The Dow Chemical Company | Fabricated articles made from ethylene polymer blends |
| US6316549B1 (en) | 1991-10-15 | 2001-11-13 | The Dow Chemical Company | Ethylene polymer fiber made from ethylene polymer blends |
| KR100253826B1 (ko) | 1991-12-30 | 2000-04-15 | 그레이스 스티븐 에스. | 에틸렌 공중합체의 중합방법 |
| DE4206714A1 (de) * | 1992-03-04 | 1993-09-09 | Sandoz Ag | Wachsdispersionen, deren herstellung und verwendung |
| US5238892A (en) | 1992-06-15 | 1993-08-24 | Exxon Chemical Patents Inc. | Supported catalyst for 1-olefin(s) (co)polymerization |
| US6448341B1 (en) | 1993-01-29 | 2002-09-10 | The Dow Chemical Company | Ethylene interpolymer blend compositions |
| BR9405715A (pt) | 1993-01-29 | 1995-11-28 | Dow Chemical Co | Processo para preparar um composição de interpolímero de etileno/a-olefina e composição de interpolímero de etileno/a-olefina |
| US5419960A (en) | 1993-04-30 | 1995-05-30 | Mobil Oil Corp. | Coated films with good low temperature sealing properties an hot tack |
| DE69431222T2 (de) | 1993-06-07 | 2003-04-17 | Mitsui Chemicals, Inc. | Übergangsmetallverbindung, und diese enthaltender Polymerisationkatalysator |
| US5360648A (en) | 1993-06-24 | 1994-11-01 | The Dow Chemical Company | Pouch for packaging flowable materials |
| JPH07233341A (ja) | 1994-02-23 | 1995-09-05 | Nippon Parkerizing Co Ltd | 自己析出型水性コーティング組成物 |
| WO1995032235A1 (en) | 1994-05-24 | 1995-11-30 | Exxon Chemical Patents Inc. | Improved propylene copolymer heat seal resin and articles therefrom |
| DE4428382C2 (de) | 1994-08-11 | 1996-09-19 | Henkel Kgaa | Verwendung eines wäßrigen Primers für unpolare Kunststoffe |
| US5545504A (en) | 1994-10-03 | 1996-08-13 | Xerox Corporation | Ink jettable toner compositions and processes for making and using |
| US5792534A (en) | 1994-10-21 | 1998-08-11 | The Dow Chemical Company | Polyolefin film exhibiting heat resistivity, low hexane extractives and controlled modulus |
| JP2759620B2 (ja) * | 1995-01-31 | 1998-05-28 | 株式会社神戸製鋼所 | 樹脂塗装金属板及びその製造方法 |
| GB9505658D0 (en) | 1995-03-21 | 1995-05-10 | Univ London | Hormone and growth factor mimetics |
| ZA963193B (en) | 1995-04-27 | 1996-10-25 | Coutaulds Films Holdings Limit | Heat sealed polymeric films |
| US5539021A (en) | 1995-06-05 | 1996-07-23 | The Dow Chemical Company | Process for preparing high internal phase ratio emulsions and latexes derived thereof |
| US5574091A (en) | 1995-06-05 | 1996-11-12 | The Dow Chemical Comapny | Aqueous dispersions of olefin copolymers |
| US6221191B1 (en) | 1996-06-07 | 2001-04-24 | Qpf, L.L.C. | Polyester-containing biaxially-oriented polypropylene films and method of making the same |
| US5635248A (en) * | 1995-06-07 | 1997-06-03 | Rohm And Haas Company | Method of producing coating on reconstituted wood substrate |
| US5869575A (en) | 1995-08-02 | 1999-02-09 | The Dow Chemical Company | Ethylene interpolymerizations |
| TW421626B (en) | 1995-09-12 | 2001-02-11 | Dow Chemical Co | Pouches for packaging flowable materials |
| US5879768A (en) | 1995-10-06 | 1999-03-09 | The Dow Chemical Company | Pouches for packaging flowable materials |
| US5721025A (en) | 1995-12-05 | 1998-02-24 | The Dow Chemical Company | Pouches for packaging flowable materials in pouches |
| US6525157B2 (en) | 1997-08-12 | 2003-02-25 | Exxonmobile Chemical Patents Inc. | Propylene ethylene polymers |
| US5938437A (en) | 1998-04-02 | 1999-08-17 | Devincenzo; John | Bony anchor positioner |
| JP5144860B2 (ja) | 1998-07-02 | 2013-02-13 | エクソンモービル・ケミカル・パテンツ・インク | プロピレン−オレフィンコポリマー |
| DE19831278A1 (de) | 1998-07-13 | 2000-01-27 | Borealis Ag | Heterophasige Polyolefinlegierungen |
| US6448321B1 (en) | 1998-07-16 | 2002-09-10 | Mitsui Chemicals, Inc. | Aqueous dispersion, its production method, and its use |
| US6130266A (en) | 1999-02-04 | 2000-10-10 | Kaneka Corporation | Pre-expanded particles of propylene resin, process for preparing the same and flow-restricting device |
| US6528574B1 (en) | 1999-03-11 | 2003-03-04 | E. I. Du Pont De Nemours And Company | Blends of aqueous dispersions of fluoropolymers and aqueous dispersions of ethylene/acid or ionomeric copolymers |
| US6143825A (en) * | 1999-05-14 | 2000-11-07 | Montell Technology Company Bv | Adhesive propylene polymer compositions suitable for coating substrates |
| US6448621B1 (en) | 1999-06-04 | 2002-09-10 | Mrinal Thakur | Sensor apparatus using an electrochemical cell |
| WO2001009259A1 (en) * | 1999-07-30 | 2001-02-08 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
| AU771282B2 (en) * | 1999-07-30 | 2004-03-18 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
| US6455636B2 (en) | 2000-01-19 | 2002-09-24 | Sumitomo Chemical Company, Limited | Thermoplastic resin composition |
| GB0004898D0 (en) | 2000-03-02 | 2000-04-19 | Ici Plc | Extrusion process |
| AU2001272386A1 (en) | 2000-05-03 | 2001-11-12 | Heinz Stemmler Jr. | Composition for coating sausages and hard cheeses |
| AU2001270858A1 (en) | 2000-07-17 | 2002-01-30 | Smithkline Beecham Plc | Novel processes for the preparation of 4-phenylpiperidine derivatives |
| EP1312654B1 (en) | 2000-07-31 | 2006-05-03 | Mitsui Chemicals, Inc. | Aqueous dispersion composition for imparting chipping resistance |
| JP2002047444A (ja) | 2000-08-01 | 2002-02-12 | Mitsui Chemicals Inc | ガスバリア性皮膜形成性組成物、ガスバリア性付与方法及び付与物 |
| US6548600B2 (en) | 2000-09-22 | 2003-04-15 | Dupont Dow Elastomers L.L.C. | Thermoplastic elastomer compositions rheology-modified using peroxides and free radical coagents |
| JP4968993B2 (ja) | 2000-09-28 | 2012-07-04 | ユニチカ株式会社 | ポリエステル樹脂水性分散体およびその製造方法 |
| GB0025213D0 (en) | 2000-10-14 | 2000-11-29 | Avecia Bv | Polyester polymer compositions |
| WO2002055598A1 (en) * | 2001-01-15 | 2002-07-18 | Unitika Ltd. | Aqueous polyolefin resin dispersion |
| JP3699935B2 (ja) * | 2001-01-15 | 2005-09-28 | ユニチカ株式会社 | ポリオレフィン樹脂水性分散体及びその製造方法 |
| US20020146509A1 (en) | 2001-02-06 | 2002-10-10 | Kodokian George K. | Micronization process and polymer particles produced therefrom |
| JP2002241957A (ja) | 2001-02-14 | 2002-08-28 | Nippon Paint Co Ltd | 金属表面処理剤、金属表面処理方法および表面処理金属材料 |
| EP1234862B1 (en) * | 2001-02-22 | 2007-04-11 | Rohm And Haas Company | Aqueous coating composition |
| US6887909B2 (en) | 2001-03-30 | 2005-05-03 | Kansai Paint Co., Ltd. | Processes for producing aqueous alkyd resin dispersions |
| US6623866B2 (en) | 2001-04-04 | 2003-09-23 | Exxonmobil Oil Corporation | Multilayer films including anti-block |
| EP1377616A1 (en) | 2001-04-12 | 2004-01-07 | ExxonMobil Chemical Patents Inc. | Propylene ethylene copolymers |
| JPWO2003025058A1 (ja) | 2001-09-12 | 2004-12-24 | 住友精化株式会社 | エチレン／ビニルアルコール系共重合体水性分散液 |
| WO2003027170A1 (de) | 2001-09-15 | 2003-04-03 | Siemens Axiva Gmbh & Co. Kg | Verfahren zur herstellung feinster partikel aus schmelzbaren feststoffen |
| US20040027593A1 (en) | 2001-10-12 | 2004-02-12 | David Wilkins | Techniques for resolution independent rendering of images |
| US6960635B2 (en) | 2001-11-06 | 2005-11-01 | Dow Global Technologies Inc. | Isotactic propylene copolymers, their preparation and use |
| JP2005508415A (ja) | 2001-11-06 | 2005-03-31 | ダウ グローバル テクノロジーズ インコーポレイティド | アイソタクチックプロピレンコポリマー類、その製法および用途 |
| US20030157354A1 (en) | 2002-02-15 | 2003-08-21 | Van Veghel Michael W. | Transparent, coated, shrinkable, oriented polypropylene film |
| CN1264908C (zh) * | 2002-04-26 | 2006-07-19 | 三菱化学株式会社 | 聚丙烯类水性分散体、聚丙烯类复合水性乳液组合物及其用途 |
| US20050124753A1 (en) * | 2002-04-26 | 2005-06-09 | Mitsubishi Chemical Corporation | Polypropylene type aqueous dispersion, polypropylene type composite aqueous emulsion composition and its use |
| TWI234503B (en) | 2002-08-26 | 2005-06-21 | Jsr Corp | Composition for polishing pad and using this polishing pad |
| US7579407B2 (en) | 2002-11-05 | 2009-08-25 | Dow Global Technologies Inc. | Thermoplastic elastomer compositions |
| JP5174057B2 (ja) * | 2003-04-18 | 2013-04-03 | ユニチカ株式会社 | 塩素化ポリオレフィン樹脂水性分散体 |
| KR101009945B1 (ko) * | 2003-05-22 | 2011-01-20 | 유니티카 가부시끼가이샤 | 폴리올레핀 수지 수성 분산체, 그 제조방법 및 이것을이용한 수성 도료 |
| US7416094B2 (en) * | 2003-07-01 | 2008-08-26 | Leonard R. Sokola, Sr. | Dinnerware with attached figure and diet reminder |
| US8779053B2 (en) * | 2003-08-25 | 2014-07-15 | Dow Global Technologies Llc | Coating compositions |
| US7803865B2 (en) | 2003-08-25 | 2010-09-28 | Dow Global Technologies Inc. | Aqueous dispersion, its production method, and its use |
| US8357749B2 (en) * | 2003-08-25 | 2013-01-22 | Dow Global Technologies Llc | Coating composition and articles made therefrom |
| US9169406B2 (en) * | 2003-08-25 | 2015-10-27 | Dow Global Technologies Llc | Coating compositions |
| US7763676B2 (en) | 2003-08-25 | 2010-07-27 | Dow Global Technologies Inc. | Aqueous polymer dispersions and products from those dispersions |
| US8158711B2 (en) | 2003-08-25 | 2012-04-17 | Dow Global Technologies Llc | Aqueous dispersion, its production method, and its use |
| TW200517426A (en) | 2003-08-25 | 2005-06-01 | Dow Global Technologies Inc | Aqueous dispersion, its production method, and its use |
| US7947776B2 (en) | 2003-08-25 | 2011-05-24 | Dow Global Technologies Llc | Aqueous dispersion, its production method, and its use |
| US8349929B2 (en) * | 2003-08-25 | 2013-01-08 | Dow Global Technologies Llc | Coating composition and articles made therefrom |
| WO2005026275A1 (en) | 2003-09-05 | 2005-03-24 | Exxonmobil Oil Corporation | Coated substrates having good very low temperature sealing properties |
| JP5706058B2 (ja) | 2004-02-13 | 2015-04-22 | スミス アンド ネフュー オルトペディクス アクチェンゲゼルシャフト | 創傷治療組成物 |
| US7858706B2 (en) | 2004-03-17 | 2010-12-28 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
| US20050288290A1 (en) * | 2004-06-28 | 2005-12-29 | Borzilleri Robert M | Fused heterocyclic kinase inhibitors |
| JP5041661B2 (ja) * | 2004-11-02 | 2012-10-03 | 大日本塗料株式会社 | プラスチック基材用下塗塗料組成物及びその塗装方法 |
| US8287949B2 (en) * | 2005-07-07 | 2012-10-16 | Dow Global Technologies Inc. | Aqueous dispersions |
| US9547246B2 (en) | 2006-03-03 | 2017-01-17 | Dow Global Technologies Llc | Aqueous dispersions for use as toners |
| DE102006059680A1 (de) | 2006-12-18 | 2008-06-19 | Bayer Materialscience Ag | Colöserfreie, selbstvernetzende PUR-Dispersionen |
| JP5290532B2 (ja) | 2007-03-26 | 2013-09-18 | ユニチカ株式会社 | ポリエステル樹脂水分散体混合物、およびその製造方法、それから得られる皮膜形成物ならびに該皮膜を利用した包装袋 |
| JP2009091426A (ja) * | 2007-10-05 | 2009-04-30 | Unitika Ltd | 水性分散体、その製造法および積層体 |
| JP5290318B2 (ja) * | 2007-11-29 | 2013-09-18 | ダウ グローバル テクノロジーズ エルエルシー | トナーとして有用なコンパウンドおよびその形成方法 |
| EP2113541A1 (en) * | 2008-04-28 | 2009-11-04 | Borealis AG | Adhesive propylene polymer composition suitable for extrusion coating of paper substrates |
| US8592013B2 (en) * | 2009-07-24 | 2013-11-26 | Dow Global Technologies, Llc. | Coated container device, method of making the same |
| JP6225180B2 (ja) * | 2012-06-19 | 2017-11-01 | ダウ グローバル テクノロジーズ エルエルシー | 水性ブレンド組成物およびその製造方法 |
| WO2014105464A1 (en) * | 2012-12-28 | 2014-07-03 | Dow Global Technologies Llc | Coating compositions |
-
2013
- 2013-01-08 US US13/736,492 patent/US9169406B2/en not_active Expired - Lifetime
- 2013-11-20 BR BR112015011080-0A patent/BR112015011080B1/pt active IP Right Grant
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- 2013-11-20 KR KR1020157016182A patent/KR102129646B1/ko active Active
- 2013-11-20 US US14/646,512 patent/US20150299495A1/en not_active Abandoned
- 2013-11-20 EP EP17192687.6A patent/EP3293227B1/en active Active
- 2013-11-20 JP JP2015543138A patent/JP6348502B2/ja active Active
- 2013-11-20 BR BR122020004387-3A patent/BR122020004387B1/pt active IP Right Grant
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-
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- 2015-09-23 US US14/863,087 patent/US9416291B2/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998002305A1 (en) * | 1996-07-15 | 1998-01-22 | Mobil Oil Corporation | Metallized multilayer packaging film |
| CN1651239A (zh) * | 2004-02-06 | 2005-08-10 | 株式会社神户制钢所 | 树脂涂布金属板及其制造方法 |
| CN102498043A (zh) * | 2009-07-24 | 2012-06-13 | 陶氏环球技术有限责任公司 | 涂布的容器装置、其制备方法 |
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| EP2922914B1 (en) | 2017-11-01 |
| BR122020004387B1 (pt) | 2021-06-29 |
| US20140141268A1 (en) | 2014-05-22 |
| BR112015011080A2 (pt) | 2019-12-17 |
| US20150299495A1 (en) | 2015-10-22 |
| KR102129646B1 (ko) | 2020-07-02 |
| JP2016501292A (ja) | 2016-01-18 |
| US9169406B2 (en) | 2015-10-27 |
| BR112015011080B1 (pt) | 2021-01-19 |
| JP6348502B2 (ja) | 2018-06-27 |
| EP3293227A1 (en) | 2018-03-14 |
| EP3293227B1 (en) | 2021-01-06 |
| CN104822758A (zh) | 2015-08-05 |
| WO2014081841A1 (en) | 2014-05-30 |
| US20160009935A1 (en) | 2016-01-14 |
| EP2922914A1 (en) | 2015-09-30 |
| CN104822758B (zh) | 2017-11-10 |
| KR20150087345A (ko) | 2015-07-29 |
| CN107652786A (zh) | 2018-02-02 |
| US9416291B2 (en) | 2016-08-16 |
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