JP2007521996A - 容器内面のコーティング方法、および、内部コーティングを含む容器 - Google Patents
容器内面のコーティング方法、および、内部コーティングを含む容器 Download PDFInfo
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- JP2007521996A JP2007521996A JP2006553248A JP2006553248A JP2007521996A JP 2007521996 A JP2007521996 A JP 2007521996A JP 2006553248 A JP2006553248 A JP 2006553248A JP 2006553248 A JP2006553248 A JP 2006553248A JP 2007521996 A JP2007521996 A JP 2007521996A
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- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
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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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
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- B65D25/14—Linings or internal coatings
-
- 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
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
-
- 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]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Paints Or Removers (AREA)
- Details Of Rigid Or Semi-Rigid Containers (AREA)
- Laminated Bodies (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54438504P | 2004-02-12 | 2004-02-12 | |
| PCT/US2005/004330 WO2005080517A1 (en) | 2004-02-12 | 2005-02-11 | Methods of coating interior container surfaces and containers containing internal coatings |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007521996A true JP2007521996A (ja) | 2007-08-09 |
| JP2007521996A5 JP2007521996A5 (enExample) | 2008-03-27 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006553248A Withdrawn JP2007521996A (ja) | 2004-02-12 | 2005-02-11 | 容器内面のコーティング方法、および、内部コーティングを含む容器 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20050196629A1 (enExample) |
| EP (1) | EP1718709A1 (enExample) |
| JP (1) | JP2007521996A (enExample) |
| KR (1) | KR20070001160A (enExample) |
| CN (1) | CN1946819A (enExample) |
| AU (1) | AU2005214337A1 (enExample) |
| CA (1) | CA2555242A1 (enExample) |
| WO (1) | WO2005080517A1 (enExample) |
| ZA (1) | ZA200606381B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015514639A (ja) * | 2012-02-17 | 2015-05-21 | ヴァルスパー・ソーシング・インコーポレーテッド | ポリマーの官能化のための方法と材料及び官能化ポリマーを含むコーティング |
| JP2016522283A (ja) * | 2013-05-16 | 2016-07-28 | ザ コカ・コーラ カンパニーThe Coca‐Cola Company | 食品および飲料梱包用のポリマー組成物およびコーティング |
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| AR108133A1 (es) | 2016-04-15 | 2018-07-18 | Valspar Sourcing Inc | Composiciones de revestimiento que contienen copolímeros libres de estireno |
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| MX2020002136A (es) | 2017-08-25 | 2020-07-20 | Swimc Llc | Promotores y composiciones de adhesion para recipientes y otros articulos. |
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| EP3676342A4 (en) | 2017-09-01 | 2021-07-07 | Swimc LLC | MULTI-STAGE POLYMERIC LATEX, COATING COMPOSITIONS CONTAINING SUCH LATEX, AND ARTICLES WHICH ARE COATED |
| EP3450352A1 (en) * | 2017-09-01 | 2019-03-06 | PPG Industries Ohio, Inc. | Use of a coating composition |
| GB201717996D0 (en) * | 2017-10-31 | 2017-12-13 | Portal Medical Ltd | Medicament dispenser device |
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| MX2020013686A (es) | 2018-06-20 | 2021-05-27 | Ppg Ind Ohio Inc | Resina de poliéster acrilico y composición de recubrimiento acuosa que contiene la misma. |
| EP3827057A1 (en) | 2018-07-25 | 2021-06-02 | PPG Industries Ohio Inc. | An acrylic polyester resin and an aqueous or powder coating composition containing the same |
| MX2021000947A (es) | 2018-07-25 | 2021-06-23 | Ppg Ind Ohio Inc | Un producto recubierto con una composición de recubrimiento acuosa o en polvo que comprende una resina de poliéster acrílico. |
| WO2020159758A1 (en) * | 2019-01-30 | 2020-08-06 | Fujifilm Electronic Materials U.S.A., Inc. | Container and method of preparing the same |
| CN115151593B (zh) * | 2019-12-24 | 2023-10-03 | Ppg工业俄亥俄公司 | 涂料组合物 |
| WO2023012721A1 (en) * | 2021-08-05 | 2023-02-09 | Dirty Labs Inc. | Laundry product dispensing system |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4087026A (en) * | 1971-09-15 | 1978-05-02 | Petterson Tor H | Barrier package |
| FR2429062A1 (fr) * | 1978-06-22 | 1980-01-18 | Voisin Ets A | Dispositif de prelevement, de transfert et de coulee d'un metal en fusion |
| US4507339A (en) * | 1982-01-15 | 1985-03-26 | American Can Company | Coated metal container and method of making the same |
| DE3590249T1 (de) * | 1984-05-30 | 1986-06-26 | Sunstar Giken K.K., Takatsuki, Osaka | Polyurethan-Klebstoff |
| US5128387A (en) * | 1987-07-28 | 1992-07-07 | Borden, Inc. | Extensible and pasteurizable radiation curable coating for metal |
| US5128391A (en) * | 1988-02-24 | 1992-07-07 | Borden, Inc. | Extensible and pasteurizable radiation curable coating for metal containing organofunctional silane adhesion promoter |
| DE3840809A1 (de) * | 1988-11-29 | 1990-05-31 | Grace Gmbh | Verfahren zur herstellung von beschichteten bzw. lackierten behaeltern aus metall und deren verwendung |
| JPH05271614A (ja) * | 1992-01-29 | 1993-10-19 | Kansai Paint Co Ltd | 水性着色塗料組成物及びそれを用いる塗装方法 |
| DE4242518C2 (de) * | 1992-12-16 | 1996-10-02 | Bollig & Kemper | Wäßrige Polymerdispersionen für Klarlacke |
| ITTS940003U1 (it) * | 1994-03-07 | 1995-09-07 | Maurizio Chiodo | Involucro di protezione per bevende ed alimenti in genere contenuti in lattina |
| DE19625774A1 (de) * | 1996-06-27 | 1998-01-02 | Hoechst Ag | Selbstvernetzende wäßrige Dispersionen von Polyestern und Vinylpolymeren |
| DE19720292C1 (de) * | 1997-05-15 | 1998-06-04 | Ppg Industries Inc | Strahlenhärtbares Beschichtungsmittel und seine Verwendung zur Herstellung von Mehrschichtlackierungen, insbesondere zur Beschichtung von Verpackungsbehältern |
| GB9807213D0 (en) * | 1998-04-04 | 1998-06-03 | Ici Ltd | Aqueous coating composition |
| US5994462A (en) * | 1998-06-11 | 1999-11-30 | The Dexter Corporation | Solid coating compositions for powder and extrusion applications |
| US6037414A (en) * | 1998-09-02 | 2000-03-14 | E. I. Du Pont Nemours And Company | Polymeric pigment dispersant having an acrylic backbone, polyester side chains, cyclic imide groups and quaternary ammonium groups |
| US6485794B1 (en) * | 1999-07-09 | 2002-11-26 | Ecolab Inc. | Beverage container and beverage conveyor lubricated with a coating that is thermally or radiation cured |
| EP1149874A1 (en) * | 2000-04-17 | 2001-10-31 | Dainippon Ink And Chemicals, Inc. | Polymerizable unsaturated polyester resin composition |
| BR0110847B1 (pt) * | 2000-05-19 | 2012-05-29 | composição aglutinante reticulável aquosa, composição de revestimento, método de revestir um substrato, revestimento reticulado, e, composição de vedação aquosa. | |
| DE10144531B4 (de) * | 2001-09-11 | 2006-01-19 | Henkel Kgaa | UV-härtende anti-fingerprint Beschichtungen, Verfahren zum Beschichten und Verwendung eines lösmittelfreien Überzugsmittels |
| TWI254719B (en) * | 2001-09-28 | 2006-05-11 | Nippon Catalytic Chem Ind | (Meth)acrylic crosslinked fine particles and method of manufacturing the same |
| EP1485212B1 (en) * | 2002-02-12 | 2016-05-18 | Valspar Sourcing, Inc. | Method of coating a packaging container using crosslinkable polyester-polyurethane |
| US20040132895A1 (en) * | 2002-08-30 | 2004-07-08 | Ambrose Ronald R. | Compositions and methods for coating food cans |
| US7745508B2 (en) * | 2002-08-30 | 2010-06-29 | Ppg Industries Ohio, Inc. | Compositions and methods for coating food cans |
-
2005
- 2005-02-11 WO PCT/US2005/004330 patent/WO2005080517A1/en not_active Ceased
- 2005-02-11 CA CA002555242A patent/CA2555242A1/en not_active Abandoned
- 2005-02-11 US US11/056,718 patent/US20050196629A1/en not_active Abandoned
- 2005-02-11 KR KR1020067017505A patent/KR20070001160A/ko not_active Withdrawn
- 2005-02-11 EP EP20050722942 patent/EP1718709A1/en not_active Withdrawn
- 2005-02-11 JP JP2006553248A patent/JP2007521996A/ja not_active Withdrawn
- 2005-02-11 AU AU2005214337A patent/AU2005214337A1/en not_active Abandoned
- 2005-02-11 CN CNA2005800121363A patent/CN1946819A/zh active Pending
-
2006
- 2006-08-01 ZA ZA200606381A patent/ZA200606381B/xx unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015514639A (ja) * | 2012-02-17 | 2015-05-21 | ヴァルスパー・ソーシング・インコーポレーテッド | ポリマーの官能化のための方法と材料及び官能化ポリマーを含むコーティング |
| JP2016522283A (ja) * | 2013-05-16 | 2016-07-28 | ザ コカ・コーラ カンパニーThe Coca‐Cola Company | 食品および飲料梱包用のポリマー組成物およびコーティング |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005080517A1 (en) | 2005-09-01 |
| CA2555242A1 (en) | 2005-09-01 |
| AU2005214337A1 (en) | 2005-09-01 |
| US20050196629A1 (en) | 2005-09-08 |
| ZA200606381B (en) | 2007-12-27 |
| CN1946819A (zh) | 2007-04-11 |
| KR20070001160A (ko) | 2007-01-03 |
| EP1718709A1 (en) | 2006-11-08 |
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