ES2565502T3 - Métodos de recubrimiento de una lata de comida o bebida - Google Patents
Métodos de recubrimiento de una lata de comida o bebida Download PDFInfo
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- ES2565502T3 ES2565502T3 ES11169890.8T ES11169890T ES2565502T3 ES 2565502 T3 ES2565502 T3 ES 2565502T3 ES 11169890 T ES11169890 T ES 11169890T ES 2565502 T3 ES2565502 T3 ES 2565502T3
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- B65D17/00—Rigid or semi-rigid containers specially constructed to be opened by cutting or piercing, or by tearing of frangible members or portions
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- 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
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- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
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- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
- Y10T428/1393—Multilayer [continuous layer]
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- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
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- Y10T428/31681—Next to polyester, polyamide or polyimide [e.g., alkyd, glue, or nylon, etc.]
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- Y10T428/31688—Next to aldehyde or ketone condensation product
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- 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
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- 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
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- Y10T428/31696—Including polyene monomers [e.g., butadiene, etc.]
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Abstract
Un método de recubrimiento de una lata de comida o bebida, comprendiendo el método: proporcionar una composición de recubrimiento que comprende un polímero de látex polimerizado por emulsión, en la que el polímero de látex polimerizado por emulsión: (i) comprende un producto de reacción de un componente de monómero etilénicamente insaturado polimerizado en presencia de una dispersión acuosa de una sal de polímero, en el que el componente de monómero etilénicamente insaturado incluye al menos un monómero que contiene un grupo funcional oxirano, y (ii) está sustancialmente libre de bisfenol A de enlace y compuestos de glicidil éter aromático; y aplicar la composición de recubrimiento a un sustrato de metal antes o después de formar el sustrato de metal en una lata de comida o bebida o una porción de la misma.
Description
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divalente, preferentemente ciclohexileno. Se contempla que Y pueda ser tan grande como se desee para la aplicación particular, que un experto en la materia puede determinar fácilmente.
Preferentemente, Y proporciona estabilidad hidrolítica a al menos uno de los enlaces éster adyacentes a R1 en la Fórmula I. Esto puede conseguirse mediante la selección de Y que incluye un grupo estéricamente voluminoso que está en la proximidad (preferentemente dentro de dos átomos) de al menos uno de los átomos de oxígeno del éster en la Fórmula I.
En ciertas realizaciones, R1 tiene la fórmula -(C(R2)2)s- en la que s es al menos 2, y preferentemente, s es al menos 3, en la que cada R2 es como se ha definido anteriormente. Ejemplos de dichos grupos R1 incluyen, por ejemplo, neopentileno, butiletilpropileno y -CH2-CH(CH3)-CH2-.
En ciertas realizaciones, Y tiene la fórmula
-[Zw-C(R2)2-O-C(O)-R3-C(O)-O-C(R2)2-]vZw-,
en la que w es 0 o 1, v es de 1 a 10, cada R2 es como se ha definido anteriormente, cada R3 es independientemente un grupo orgánico divalente, y cada Z es independientemente un grupo orgánico divalente.
En ciertas realizaciones, R3 es un grupo alifático saturado divalente (es decir, grupo alquileno ramificado o no ramificado), un grupo alicíclico divalente, un grupo arileno, o combinaciones de los mismos. En ciertas realizaciones, R3 es un grupo alquileno(C3-C20) (ramificado o no ramificado) o un grupo fenileno.
En ciertas realizaciones, Z es un grupo alifático saturado divalente (es decir, grupo alquileno ramificado o no ramificado), un grupo alicíclico divalente, un grupo aromático divalente (es decir, un grupo arileno), o combinaciones de los mismos.
Preferentemente, Z proporciona estabilidad hidrolítica a al menos uno de los enlaces de éster adyacentes a R1 en la Fórmula I y/o a un enlace de éster adyacente contenido dentro de Y. Esto puede conseguirse por la selección de Z que incluye un grupo estéricamente voluminoso que está en la proximidad (preferentemente en el rango de dos átomos de distancia) de al menos uno de los átomos de oxígeno del éster.
En los segmentos de Fórmula I, n es preferentemente 0 (es decir, R no está presente). Si n es 1 y R está presente, sin embargo, es preferentemente un grupo alquileno(C1-C4), y más preferentemente un resto alquileno(C1-C4).
En los segmentos de Fórmula I, cada Ar tiene preferentemente menos de 20 átomos de carbono, más preferentemente menos de 11 átomos de carbono, e incluso más preferentemente menos de 8 átomos de carbono. Preferentemente, Ar tiene al menos 4 átomos de carbono, más preferentemente al menos 5 átomos de carbono, e incluso más preferentemente, al menos 6 átomos de carbono.
En ciertas realizaciones, cada Ar es un grupo fenileno. En ciertas realizaciones, cada Ar es un grupo fenileno de la fórmula -C6(R4)4-, en la que cada R4 es independientemente hidrógeno, un halógeno, o un grupo orgánico, y en la que dos grupos R4 pueden unirse para formar un anillo que contiene opcionalmente uno o más heteroátomos. En ciertas realizaciones, R4 es hidrógeno o un grupo orgánico, en las que dos grupos R4 pueden unirse para formar un anillo de 6 miembros. Preferentemente, R4 es hidrógeno.
Pueden prepararse polímeros de poliéster tales como estos mediante una variedad de métodos a partir de los compuestos de Fórmula II:
HO-Ar-Rn-C(O)-O-R1-O-C(O)-Rn-Ar-OH
en la que Ar, R, R1 y n son como se ha definido anteriormente. Dichos compuestos pueden prepararse, por ejemplo, mediante la reacción de esterificación de un mol de un diol (por ejemplo, HO-R1-OH tales como, por ejemplo, 1,4ciclohexano dimetanol, neopentilglicol, 2-butil-2-etil-1,3-propano diol, o 2-metil-1,3-propano diol) con dos moles de un ácido (por ejemplo, ácido 4-hidroxi benzoico). Como alternativa, dichos compuestos pueden prepararse, por ejemplo, mediante la reacción de transesterificación de un mol de un diol (por ejemplo, 1,4-ciclohexano dimetanol, neopentil glicol, 2-butil-2-etil-1,3-propano diol, o 2-metil-1,3-propano diol) con dos moles de un éster (por ejemplo, 4-hidroxi metil benzoato, 4-hidroxi etil benzoato, o 4-hidroxi butil benzoato).
Pueden prepararse polímeros de Fórmula I mediante métodos que implican desarrollar el peso molecular de los compuestos de Fórmula II. En ciertas realizaciones, los compuestos de Fórmula II (por ejemplo, fenoles dihídricos) pueden hacerse reaccionar con un diepóxido para desarrollar el peso molecular. Por ejemplo, compuestos de Fórmula II (por ejemplo, fenoles dihídricos) pueden hacerse reaccionar en gran medida con diepóxidos no basados en BPA y BPF de la misma manera que el Bisfenol A o Bisfenol F lo hace, para generar polímeros que pueden formularse con reticulantes y aditivos para recubrimientos para envasado rígido. Por ejemplo, los compuestos de Fórmula II pueden hacerse reaccionar con un diepóxido para formar un polímero que incluya segmentos -CH2
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soldada, cada lata requiere típicamente una capa de recubrimiento líquido, que protege la "soldadura" expuesta de la corrosión posterior u otros efectos al producto alimenticio contenido. Los recubrimientos líquidos que tienen este papel se denominan "tiras de costura lateral". Las tiras de costura lateral típicas se aplican por pulverización y se curan rápidamente con el calor residual de la operación de soldadura además de un horno térmico, ultravioleta, y/o electromagnético pequeño.
Otras aplicaciones comerciales del recubrimiento y métodos de curado también contemplan, por ejemplo, electrorrecubrimiento, recubrimiento por extrusión, laminado, recubrimiento en polvo, y similares.
Los recubrimientos preferidos de la presente invención muestran una o más de las propiedades que se han descrito en la Sección de Ejemplos. Los recubrimientos más preferidos de la presente invención muestran una o más de las siguientes propiedades: valor de exposición de metal de menos de 3 mA; valor de exposición de metal después del daño por caída de menos de 3,5 mA; resultados de extracción global de menos de 50 ppm; proporción de adhesión de 20; proporción de alteración superficial del color de al menos 7; agrietamiento leve o ausencia en un ensayo de impacto inverso; sin agrietamiento (proporción de 10) en un ensayo de impacto domo; biselado por debajo de 0,51 cm (0,2 pulgadas); intervalo COF de 0,055 a 0,095; y después de la pasteurización o esterilización en retorta, una continuidad de menos de 20 mA.
A continuación, se resumen las realizaciones divulgadas en la presente solicitud:
1. Un método de recubrimiento de una lata de comida o bebida, el método comprende:
formar una composición que comprende un polímero de látex polimerizado por emulsión, que comprende:
formar una sal de un polímero ácido- o anhídrido-funcional y una amina en un transportador que comprende agua para formar una dispersión acuosa; combinar un componente de monómero etilénicamente insaturado con la dispersión acuosa; y polimerizar el componente de monómero etilénicamente insaturado en presencia de la dispersión acuosa para formar un polímero de látex polimerizado por emulsión; y
aplicar la composición que comprende el polímero de látex polimerizado por emulsión a un sustrato de metal antes de o después de conformar el sustrato de metal en una lata de comida o bebida o parte de la misma.
- 2.
- El método del punto 1, en el que la aplicación de la composición a un sustrato de metal comprende aplicar la composición al sustrato de metal en forma de una bobina o lámina plana, endurecer el polímero de látex polimerizado por emulsión, y formar el sustrato en una lata de comida o bebida o parte de la misma.
- 3.
- El método del punto 2, en el que conformar el sustrato en una lata o parte de la misma comprende conformar el sustrato en una tapa de lata o un cuerpo de lata.
- 4.
- El método del punto 2, en el que la lata es una lata de comida embutida de 2 piezas, lata de comida de 3 piezas, tapa de lata de comida, lata embutida y planchada, tapa de lata de bebida, y similares.
- 5.
- El método del punto 1, en el que el sustrato de metal comprende acero o aluminio.
- 6.
- El método del punto 1, en el que la aplicación de la composición a un sustrato de metal comprende la aplicación de la composición al sustrato de metal después de que el sustrato de metal se forme en una lata o parte de la misma.
- 7.
- El método del punto 1, en el que la combinación de un componente de monómero etilénicamente insaturado con la dispersión acuosa comprende añadir el componente de monómero etilénicamente insaturado a la dispersión acuosa.
- 8.
- El método del punto 7, en el que el componente de monómero etilénicamente insaturado se añade progresivamente a la dispersión acuosa.
- 9.
- El método del punto 1, en el que el componente de monómero etilénicamente insaturado comprende una mezcla de monómeros.
- 10.
- El método del punto 9, en el que la mezcla de monómeros comprende al menos un monómero que contiene un grupo funcional oxirano.
- 11.
- El método del punto 10, en el que la mezcla de monómeros comprende al menos un monómero alfa, betaetilénicamente insaturado que contiene un grupo funcional oxirano.
- 12.
- El método del punto 10, en el que el monómero que contiene un grupo funcional oxirano está presente en el
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en miliamperios. Típicamente, se someten inicialmente a ensayo las continuidades de la tapa y después, las tapas se someten a pasteurización o esterilización en retorta.
Los recubrimientos preferidos de la presente invención pasan inicialmente menos de 10 miliamperios (mA) cuando
5 se someten a ensayo como se ha descrito anteriormente, más preferentemente menos de 5 mA, lo más preferible menos de 2 mA, y de forma óptima menos de 1 mA. Después de la pasteurización o esterilización en retorta, los recubrimientos preferidos proporcionan continuidades de menos de 20 mA, más preferentemente menos de 10 mA, incluso más preferentemente menos de 5 mA, e incluso más preferentemente menos de 2 mA.
10 Lista de Materias Primas e Ingredientes
La siguiente tabla enumera algunas de las materias primas e ingredientes usados en los siguientes ejemplos. Como apreciará el experto en la materia, pueden sustituirse por materiales o proveedores alternativos
- Nombre Químico
- Nombre Comercial Proveedor Ubicación
- Ácido Metacrílico Glacial
- Rohm & Haas Philadelphia, PA
- Butil Acrilato
- Rohm & Haas Philadelphia, PA
- Estireno
- Rohm & Haas Philadelphia, PA
- Peróxido de Benzoílo
- Norac Company Helena, AR
- Butanol
- Dow Midland, MI
- Butil éter de Etilenglicol
- Butyl Cellosolve/Dowanol EB Dow Midland, MI
- Butil Metacrilato
- Rohm & Haas Philadelphia, PA
- Peroctoato de t-Butilo
- Arkema Philadelphia, PA
- Etil acrilato
- Rohm & Haas Philadelphia, PA
- Ácido acrílico
- Rohm & Haas Philadelphia, PA
- Hidroxipropilmetacrilato
- ROCRYL 410 Rohm & Haas Philadelphia, PA
- Hidroxietil metacrilato
- ROCRYL 400 Rohm & Haas Philadelphia, PA
- Dimetiletanol amina
- Huntsman Chemical Dallas, TX
- Glicidil metacrilato
- SR 379 Sartomer, Inc Warrington, PA
- Peróxido de Hidrógeno
- Ashland Chemical Pittsburgh, PA
- Benzoína
- Estron Calvert City, KY
- N-Isobutoximetacrilamida
- Monómero CYLINK IBMA Cytec Ind. West Patterson, NJ
- Alcohol amílico
- Dow Midland, MI
- Butil éter de Propilenglicol
- DOWANOL PNB Dow Midland, MI
- Alcohol etoxilado secundario
- TERGITOL 15-S-7 Dow Midland, MI
- sec-butanol
- Dow Midland, MI
- Cera de Polietileno
- Slipayd 404 Elementis Staines, UK
- Fenólico basado en Fenol Termoestable
- SD-912B Valspar Minneapolis, MN
- Emulsión de cera de Carnuba
- Michemlube 160 PFE Michelman Cincinnati, OH
- Alcohol isooctílico
- Aldrich Chemical Milwaukee, WI
- Cera de Polietileno
- Lanco Glidd 5118 Lubrizol Wickliffe, OH
- Dipropilenglicol
- Aldrich Chemical Milwaukee, WI
- Ácido Isoftálico
- BP Amoco Chicago, IL
- Óxido de Dibutil estaño
- Fastcat 4201 Arkema Philadelphia, PA
- Xileno
- Exxon Newark, NJ
- Anhídrido Trimelítico
- BP Amoco Chicago, IL
- Complejo de Hierro
- Hamp-OL 4,5 % Iron Traylor Chemical Orlando, FL
- Ácido eritórbico
- Aldrich Chemical Milwaukee, WI
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- Nombre Químico
- Nombre Comercial Proveedor Ubicación
- T-Butilhidoperóxido
- Trigonox A-W70 Akzo Philadelphia, PA
- Etilenglicol
- Ashland Chemical Pittsburgh, PA
- Ácido sebácico
- Ivanhoe Indutries Tampa. FL
- 1,4-ciclohexano dimetanol al 90 % en agua
- CHDM-90 Eastman Kingsport, TN
- Ácido Buti Estanoico
- Fastcat 4100 Arkema Philadelphia, PA
- Ácido 4-Hidroxibenzoico
- Acros Organics through Fisher Scientific Houston, TX
- Diglicidil éter de 1,4ciclohexano dimetanol
- Erisys GE-22 CVC Specialty Chemicals Maple Shade, NJ
- Yoduro de etiltrifenil fosfonio
- Catalyst 1201 Deepwater Chemicals Woodward, OK
- Anhídrido succínico
- JLM Marketing Tampa, FL
- Bisfenol A
- Dow Midland, MI
- Diglicidil éter de Bispenol A
- Epon 828 Resolution Performance Products Houston, TX
- Metilisobutil cetona
- Dow Midland, MI
- Éster dibásico
- Dupont Wilminton, DE
- Metil éter de propilenglicol
- Dowanol PM Dow Midland, MI
Ejemplo de Referencia 1: Realización 1. Preparación de Acrílico Ácido-Funcional
Se preparó una premezcla de 512,6 partes de ácido metacrílico glacial (MAA), 512,6 partes de acrilato de butilo (BA), 114,0 partes de estireno, y 73,2 partes de peróxido de benzoílo (humedad al 70 %) en un recipiente separado. Se equipó un matraz de 3 litros con un agitador, condensador de reflujo, termopar, manta calefactora, y una atmósfera protectora de nitrógeno. Se añadió el diez por ciento de la premezcla al matraz junto con 405,9 partes de butanol y 30,6 partes de agua desionizada. A la premezcla restante se añadieron 496,1 partes de butanol y 38,3 partes de agua desionizada. Con la atmósfera protectora de nitrógeno fluyendo en el matraz, los contenidos se calentaron a 93 ºC. A 93 ºC, el calentamiento externo se detuvo y se dejó que el material aumentase su temperatura durante quince minutos. Después de quince minutos, el lote estaba a 97 ºC, y la premezcla restante se añadió uniformemente durante dos horas manteniendo de 97 ºC a 100 ºC. Cuando la adición de premezcla se completó, el recipiente de premezcla se aclaró con 5 partes de butanol. El lote se mantuvo a la misma temperatura durante dos horas y media. El calentamiento fue discontinuo y se añadieron 317,7 partes de butil cellosolve. El prepolímero acrílico resultante tuvo sólidos (NV) al 44,3 %, con un índice de acidez de 313 y una viscosidad Brookfield (según se determina por la norma ASTM D-2196) de 4.990 centipoise (cps).
Ejemplo de Referencia 1: Realización 2. Preparación de Acrílico Ácido-Funcional
Se preparó una premezcla de 677,7 partes de ácido metacrílico glacial, 677,7 partes de metacrilato de butilo (BMA), 150,8 partes de estireno, y 96,9 partes de peróxido de benzoilo (humedad al 70 %) se preparó en un recipiente separado. Se equipó un matraz de 5 litros con un agitador, condensador de reflujo, termopar, manta calefactora, y una atmósfera protectora de nitrógeno. Se añadió el diez por ciento de la premezcla al matraz junto con 536,9 partes de butanol y 40,7 partes de agua desionizada. A la premezcla restante se añadieron 758,1 partes de butanol y 50,6 partes de agua desionizada. Con la atmósfera protectora de nitrógeno fluyendo en el matraz, los contenidos se calentaron a 93 ºC. A 93 ºC, el calentamiento externo se detuvo y se dejó que el material aumentase su temperatura durante diez minutos. Después de diez minutos, el lote estaba a 98 ºC, y la premezcla restante se añadió uniformemente durante dos horas manteniendo de 97 ºC a 100 ºC. El lote se mantuvo a la misma temperatura durante tres horas. El calentamiento fue discontinuo y el lote se enfrió. El prepolímero acrílico resultante tuvo NV al 49,9 %, con un índice de acidez de 304 y una viscosidad Brookfield de 101.000 centipoise.
Ejemplo de Referencia 1: Realización 3. Preparación de Acrílico Ácido-Funcional
Se preparó una premezcla de 802,6 partes de ácido metacrílico glacial, 807 partes de metacrilato de butilo, 178,5 partes de estireno, 80,3 partes de peroctoato de t-butilo, 838,5 partes de butanol y 59,9 partes de agua desionizada en un recipiente separado. Se equipó un matraz de 5 litros con un agitador, condensador de reflujo, termopar, manta calefactora, y una atmósfera protectora de nitrógeno. Se añadieron al matraz de 5 litros 635,8 partes de butanol y 48,1 partes de agua desionizada. El matraz se calentó a 94 ºC. A 94 ºC, se añadieron 12,5 partes de peroctoato de t-butilo. El lote se mantuvo durante cinco minutos después de lo cual la premezcla se añadió durante dos horas y
21
Tabla 5: Experimento de Diseño de Emulsión
- Ejemplo 3:
- Realización 11 Realización 12 Realización 13 Realización 14 Realización 15 Realización 16 Realización 17 Realización 18
- Proporción Acrílico/ Monómero
- 73/27 65/35
- Composición de Monómero 1
- Composición de Monómero 2 Composición de Monómero 1 Composición de Monómero 2
- Nivel GMA
- Bajo Alto Bajo Alto Bajo Alto Bajo Alto
- Monómeros
- Estireno
- 42 39 33 33 43 41 33 33
- BA
- 54 53 40 41 54 53 40 40
- BMA
- 0 0 23 18 0 0 24 21
- GMA
- 4 8 4 8 3 6 3 6
- 32,0 %l
- 31,3 % 31,6 % 31,9 % 31,6 % 32,0 % 31,7 % 32,0 %
- Viscosidad (Copa Ford n.º 4)
- -- 63 s -- -- 35 s 210 s 42 s ---
- Viscosidad Brookfield (cps)
- 10.000 -- 10.000 695 -- -- -- 1.384
- Índice de acidez
- 74,7 72,9 74,9 70,2 101 96,1 101 96,5
Se sometieron a ensayo las estructuras reticulares de la Tabla 5 sin modificación o formulación adicional, y los resultados se muestran en la Tabla 6. Cada composición se depositó sobre aluminio Alcoa ALX con un peso de película de 1,1-1,25 miligramos por centímetro cuadrado (mg/cm2) (7-8 miligramos por pulgada cuadrada (msi)) y se curó durante 10 segundos para conseguir un pico de temperatura de metal de 215 ºC (420°F) en un horno de bobina alimentado por gas.
Tabla 6: Rendimiento de Película de Tapa de Bebida
- Control basado en agua1
- Ej. 3: Realización 11 Ej. 3: Realización 12 Ej. 3: Realización 13 Ej. 3: Realización 14 Ej. 3: Realización 15 Ej. 3: Realización 16 Ej. 3: Realización 17 Ej. 3: Realización 18
- Agrietamiento
- Ninguno Ninguno Ninguno Ninguno Ninguno Ninguno Leve Ninguno Ninguno
- Resistencia MEK
- 19 5 6 3 7 5 6 4 8
- Biselado4
- 0,343 0,013 0,020 0,071 0,003 0,020 0,013 0,030 0,013
- Retorta de Agua2
- Alteración superficial del color
- 9,5 10 9,5 9,5 9,5 9 10 8 10
- Adhesión
- 10 10 10 10 10 10 10 10 10
- Pasteurizaión3
- Alteración superficial del color
- 10 10 10 10 10 10 10 10 10
- Adhesión
- 10 10 10 10 10 10 10 10 10
- Continuidad de la Tapa
- Inicial
- 0 0,22 25,3 11,5 57,8 17,7 133,5 27,5 132,2
- Después de Retorta2
- 8,4 31,8 No Sometido a Ensayo 31,7 No Sometido a Ensayo No Sometido a Ensayo No Sometido a Ensayo 34,3 No Sometido a Ensayo
- 1 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 13Q80AG. 2 90 minutos a 121 ºC (250 ºF). 3 30 minutos a 85 ºC (185 ºF). 4 Realizado después de una pasteurización de 45 minutos a 85 ºC (185 ºF). Medido en centímetros.
10 Ejemplo 3: Realizaciones 5b y 19-25
Se preparó un diseño de experimento según el Ejemplo 2: La realización 4, como sal acrílica de ácido funcional y el proceso que se ha indicado anteriormente se describe en la Tabla 7. El Ejemplo 3: Realización 5b, se incluyó como 15 una de las variables y fue una repetición de la Realización 5.
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Tabla 7: Experimento de Diseño de Emulsión
- Ejemplo 3:
- Realización 19 Realización 20 Realización 5b Realización 21 Realización 22 Realización 23 Realización 24 Realización 25
- Proporción Acrílico/Monóm ero
- 73/27 65/35
- Composición de Monómero 1
- Composición de Monómero 2 Composición de Monómero 1 Composición de Monómero 2
- Nivel GMA
- Bajo Alto Bajo Alto Bajo Alto Bajo Alto
- Monómeros
- Estireno
- 42 39 33 33 43 41 33 33
- BA
- 54 53 40 41 54 53 40 40
- BMA
- 0 0 23 18 0 0 24 21
- GMA
- 4 8 4 8 3 6 3 6
- Sólidos
- 31,5 % 31,6 % 31,6 % 31,4 % 31,3 % 31,6 % 31,5 % 31,7 %
- Viscosidad (Copa Ford n.º 4)
- 55 s 60 s 50 s 56 s 106 s --- 70 s ---
- Viscosidad Brookfield (cps)
- --- --- --- --- --- 2.624 --- 3.000
- Índice de acidez
- 71,9 73,0 69,0 68,3 95,4 92,5 94,7 98,0
Las estructuras reticulares a partir de la Tabla 7 se cometieron a ensayo sin modificación o formulación adicional, y los resultados se muestran en la Tabla 8. Cada composición se depositó sobre aluminio Alcoa ALX con un peso de lámina de 1,1-1,25 mg/cm2 (7-8 msi) y se curó durante 10 segundos para conseguir un pico de temperatura de metal de 215 ºC (420 ºF) en un horno de bobina alimentado por gas.
Tabla 8. Rendimiento de Película de Tapa de Bebida
- Control basado en agua1
- Ej. 3: Realización 19 Ej. 3: Realización 20 Ej. 3: Realización 5b Ej. 3: Realización 21 Ej. 3: Realización 22 Ej. 3: Realización 23 Ej. 3: Realización 24 Ej. 3: Realización 25
- Agrietamiento
- Ninguno Ninguno Ninguno Ninguno Ninguno Ninguno Leve Ninguno Sí
- MEK
- 19 4 7 4 10 6 11 4 6
- Biselado4
- 0,343 0,064 0,051 0,038 0,033 0,056 0,013 0,046 0,013
- Retorta de Agua2
- Alteración superficial del color
- 9,5 9,5 9,5 10 10 9,5 10 7 9,5
- Adhesión
- 10 10 10 10 10 10 10 10 10
- Pasteurizaión3
- Alteración superficial del color
- 10 10 10 10 10 10 10 10 10
- Adhesión
- 10 10 10 10 10 10 10 10 10
- Continuidad de la Tapa
- Inicial
- 0 5,5 2,6 6,0 12,3 20,2 61,2 1,9 93,6
- Después de Retorta2
- 8,4 23,5 143 23,4 134,0 78,8 No Sometido a Ensayo 52,5 No Sometido a Ensayo
- 1 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 13Q80AG. 2 90 minutos a 121 ºC (250 ºF). 3 30 minutos a 85 ºC (185 ºF). 4 Realizado después de una pasteurización de 45 minutos a 85 ºC (185 ºF). Medido en centímetros.
10 Ejemplo 3: Realizaciones 26-33 Se preparó un diseño de experimento según el Ejemplo 2: La realización 11 como la sal acrílica de ácido funcional y el proceso que se ha indicado anteriormente se describe en la Tabla 9. 15
27
- Control basado en agua1
- Ejemplo 4: Realización 3 Ejemplo 4: Realización 4
- Impacto en Domo
- 10 10 10
- Resistencia a Isopropanol
- >100 >100 5 - 10
- Retorta de Agua2
- Alteración superficial del color
- 7 10 10
- Adhesión
- 10 10 10
- Ensayo de Detergente Joy
- Alteración superficial del color
- 7 10 10
- Adhesión
- 10 10 10
- Extracciones globales3
- <0,1 ppm4 <0,1 ppm4 <0,1 ppm4
- 1 Recubrimiento de lata de bebida interior disponible comercialmente de Valspar código 10Q45AF. 2 90 minutos a 121 ºC (250 ºF). 3 2 horas a 65,56 ºC (150 ºF) en etanol acuoso al 90 %. 4 Por debajo del límite de detección de corriente.
Como se puede ver en la Tabla 17, los recubrimientos de la presente invención se comparan de forma favorable al recubrimiento de epoxi-acrilato comercial, y existe un beneficio sustancial en la resistencia a retorta.
5 Ejemplo 5: Realización 1. Recubrimiento de Bobina de la Tapa de Bebida
Se agitaron en un tarro con un agitador, 483,25 partes de la emulsión del Ejemplo 3: Realización 5 con 16,75 partes de cera SLIPAYD 404. La mezcla se agitó durante 10 minutos para hacerla uniforme. Después, la mezcla se filtró. La mezcla tuvo aproximadamente sólidos al 31 %. La mezcla se aplicó a 7-8 miligramos por pulgada cuadrada (msi)
10 (1,1-1,25 mg/cm2) sobre aluminio ALX Alcoa y se secó en horno durante 10 segundos (s) para conseguir un pico de temperatura de metal de 204 ºC (400 ºF) en un horno de bobina. También se aplicó a 7-8 msi (1,1-1,25 mg/cm2) sobre aluminio ALX Alcoa y se secó en horno durante 10 segundos para conseguir un pico de temperatura de metal de 224 ºC (435 ºF) en un horno de bobina. Las propiedades de película se muestran en la Tabla 18.
15 Tabla 18: Propiedades de Película de Tapa de Bebida
- Control basado en agua1
- Ejemplo 5 Realización 1
- Secado en horno
- 10 s para conseguir 204 ºC (400 ºF) 10 s para conseguir 224 ºC (435 ºF) 10 s para conseguir 204 ºC (400 ºF) 10 s para conseguir 224 ºC (435 ºF)
- Res. MEK
- 23 35 4 4
- Biselado2
- 0,500 0,193 0,018 0,010
- Dowfax3
- Alteración superficial del color
- 4 9 4 9
- Adhesión
- 10 10 10 10
- Pasteurización 4
- Alteración superficial del color
- 6 9 5 10
- Adhesión
- 10 10 10 10
- Retorta de Agua5
- Alteración superficial del color
- 6,5 10 5,5 10
- Adhesión
- 10 10 10 10
- Continuidades de Tapa
- Inicial Después Inicial Después Inicial Después Inicial Después
- Pasteurización4
- 0,13 0,33 0,06 0,28 2,76 21,35 1,5 17,9
- Retorta de Agua5
- 0,016 2,22 0,06 0,52 4,16 22,9 1,4 17,55
- 1 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 13Q80AG.
33
Tabla 21: Formulación de Tapa de Bebida
- Ejemplo 5 Realización 5
- Composición
- Ejemplo 3, Realización 38
- 90,80
- Dowanol PNP 1
- 2,425
- Dowanol DPNB 1
- 2,425
- Alcohol Isooctílico
- 1,54
- Michem Lube 160 PFE
- 0,57
- Lanco Glidd 5118 2
- 2,24
- Sólidos (%)
- 27,5 - 29,5
- Viscosidad (Copa Ford n.º 4)
- 20 s - 30 s
- 1 Disponible comercialmente de Dow Chemical 2 Lubricante disponible comercialmente de Lubrizol Corp.
Tabla 22: Rendimiento de Película de la Formulación de Tapa de Bebida
- Control Basado en Agua1
- Ejemplo 5 Realización 5
- Secado en horno
- 10 s para conseguir 204 ºC (400 ºF) 10 s para conseguir 215 ºC (420 ºF) 10 s para conseguir 204 ºC (400 ºF) 10 s para conseguir 215 ºC (420 ºF)
- Res. MEK
- 34 40 10 8
- Biselado4
- 0,178 0,094 0,074 0,038
- Dureza al Lápiz
- 3H - 4H 3H HB HB
- COF
- 0,068 0,076 0,068 0,075
- Pasteurización2
- Alteración superficial del color
- 10 10 9 10
- Adhesión
- 10 10 10 10
- Retorta de Agua3
- Alteración superficial del color
- 9 10 8 9
- Adhesión
- 10 10 10 10
- Continuidades de Tapa
- Inicial Después Inicial Después Inicial Después Inicial Después
- Pasteurización2
- 0,0 0,1 1,1 17,6 0,5 0,7 0,5 4,3
- Retorta de Agua3
- 0,05 0,15 1,4 11,2 0,15 0,35 0,78 10,5
- 1 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 13Q80AG. 2 30 minutos a 85 ºC (185 ºF). 3 90 minutos a 121 ºC (250 ºF). 4 Realizado después de una pasteurización de 45 minutos a 85 ºC (185 ºF). Medido en centímetros.
5 Los resultados a partir de la Tabla 22 muestran que una formulación de tapa de bebida de la presente invención puede proporcionar un rendimiento similar a un recubrimiento de tapa de bebida acuoso basado en epoxi comercial incluso con una resistencia de disolvente menor como se mide por dobles frotamientos MEK. También hay un beneficio adicional en una mejor resistencia al biselado.
10 Ejemplo 6: Látex con Estabilizador de Poliéster
El Ejemplo 6 se diseña para ilustrar que el uso de una sal de polímero ácido-funcional diferente como estabilizador para una emulsión de la presente invención. 15 Etapa A
Se equipó un matraz de 2 litros con un agitador, columna de relleno, colector Dean Stark, condensador de reflujo, termopar, manta calefactora, y una atmósfera protectora de nitrógeno. Al matraz se añadieron 700,1 partes de
35
premezcla de monómero se aclaró con 81,6 partes de agua desionizada, que se añadió también al matraz. Los contenidos del matraz se agitaron durante 10 minutos, después de lo cual se añadió el 10 % de la tercera premezcla dentro de un minuto. Una vez que estuvo el 10 % de la tercera premezcla, la temperatura se aumentó a 37 ºC y el lote se mantuvo durante cinco minutos. Después de cinco minutos, la cantidad restante de la tercera premezcla se
5 añadió durante 45 minutos. La temperatura se dejó aumentar sin calor externo aplicado. Durante la adición la temperatura máxima fue de 57 ºC. Después de que la adición se completara la temperatura fue de 51 ºC. El control de temperatura se ajustó a 52 ºC. La tercera premezcla se aclaró con 108,4 partes de agua desionizada y se añadió al lote. El lote se mantuvo durante 1,5 horas y se enfrío después. Este proporcionó una emulsión al 33,1 % en sólidos, índice de acidez de 27,1, pH de 7,9, y una viscosidad de 12 s (Copa Ford Número 4).
10 Etapa D
Se añadieron a 1473,75 partes de la emulsión de la Etapa C, 26,25 partes de DMEOA para aumentar el pH a 8,6. Usando 1330,18 partes de este material de pH aumentado, se añadieron 89,51 partes de etilenglicol, 16,65 partes
15 de éster dibásico, 16,67 partes de DOWANOL PM, 5,17 partes de xileno, 17,5 partes de una solución de sólidos al 50 % de un fenólico fenol-formaldehído, y 24,57 partes de MICHEM 160 PFE. Se determinó esta formulación para que tuviera sólidos al 30,1 %, viscosidad Ford Número 4 de 12 segundos y 1,05 kg/l (8,75 libras por galón).
La composición de la Etapa D se aplicó a paneles de aluminio sin cromo y se secó en horno durante 10 segundos
20 para conseguir un pico de temperatura de metal de 215 ºC (420 ºF). Un segundo conjunto se secó en horno durante 10 segundos para conseguir un pico de temperatura de metal de 227 ºC (440 ºF). Los resultados del ensayo de la tapa de bebida de este ejemplo, frente a unas fórmulas de control basadas en agua y basadas en disolvente comerciales, se muestran en las Tablas 26 y 27.
- Tabla 26
- Ensayo Comparativo de Curado del Ejemplo 9 Etapa D a 215 ºC (420 ºF)
- Control basado en Agua1
- Control basado en Disolvente2 Ejemplo 9 Etapa D
- MEK
- 44 34 38
- Biselado3
- 0,0457 0,0457 0,000
- COF
- 0,061 0,066 0,063
- Pasteurización4
- Alteración superficial del color
- 10 10 8 a 96
- Adhesión
- 10 10 10
- Retorta de Agua5
- Alteración superficial del color
- 10 10 4 a 106
- Adhesión
- 10 10
- Continuidad de Tapa
- Inicial Después Inicial Después Inicial Después
- Pasteurización
- 0,08 0,12 0,0 0,30 0,0 0,5
- Retorta de Agua
- 0,10 0,4 0,02 0,72 0,27 1,2
- 1 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 13Q80AG. 2 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 92X205S. 3 Realizado después de una pasteurización de 45 minutos a 85 ºC (185 ºF). Medido en centímetros (cm). 4 30 minutos a 85 ºC (185 ºF). 5 90 minutos a 121 ºC (250 ºF). 6 Alteración superficial del color inicial observada que mejora dentro de 5 minutos.
39
- Tabla 27
- Ensayo Comparativo de Curado del Ejemplo 9 Etapa D a 227 ºC (440 ºF)
- Control basado en Agua1
- Control basado en Disolvente2 Ejemplo 9 Etapa D
- MEK
- 52 37 40
- Biselado3
- 0,0559 0,0356 0,000
- COF
- 0,059 0,065 0,063
- Pasteurización4
- Alteración superficial del color
- 10 10 8 a 106
- Adhesión
- 10 10 10
- Retorta de Agua5
- Alteración superficial del color
- 10 10 6 a 106
- Adhesión
- 10 10
- Continuidad de Tapa
- Inicial Después Inicial Después Inicial Después
- Pasteurización
- 0,0 0,48 0,07 0,23 0,1 0,8
- Retorta de Agua
- 0,05 0,4 0,25 1,5 0,35 0,8
- 1 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 13Q80AG. 2 Recubrimiento de tapa de bebida disponible comercialmente de Valspar código 92X205S. 3 Realizado después de una pasteurización de 45 minutos a 85 ºC (185 ºF). Medido en cm. 4 30 minutos a 85 ºC (185 ºF). 5 90 minutos a 121 ºC (250 ºF). 6 Alteración superficial del color inicial observada que mejora dentro de 5 minutos.
Ejemplo 10
5 El Ejemplo 10 ilustra el uso de una sal de polímero ácido-funcional diferente como estabilizador para una emulsión de la presente invención.
Etapa 1
10 Se colocan aproximadamente 1055 partes de BPA en un matraz junto con aproximadamente 1684 partes de resina epoxi líquida (EPON 828), 85 partes de metil isobutil cetona, y de 2 a 3 partes de Catalyst 1201. La temperatura se ajusta a 160 ºC y los contenidos se calientan después durante aproximadamente tres horas para conseguir un valor epoxi del material de aproximadamente 0,003. El lote se ajusta después para que tenga 2684,2 partes de este
15 material en el matraz. Añadido al matraz hay 145,0 partes de metil isobutil cetona y 294,7 partes de anhídrido succínico. La temperatura se mantiene a 120-135 ºC durante dos horas. Después de mantener dos horas, se añaden 124,8 partes de agua desionizada y una premezcla de 214,2 partes de DMEA con 265,8 partes de agua desionizada. Después, se añaden 6325,8 partes de agua desionizada. El material se enfría, y debería dar como resultado un producto con valores objetivo de sólidos del 26 % al 27 %, un índice de acidez de aproximadamente 72,
20 un pH de aproximadamente 7 a 9, y una viscosidad Ford Número 4 de 15 Segundos. Este material se usa en la Etapa 2.
Etapa 2
25 Se equipa un matraz de 5 litros con un agitador, condensador de reflujo, termopar, manta calefactora, y una atmósfera protectora de nitrógeno. En el matraz se añaden aproximadamente 1183 partes del material de la Etapa 1 y 780 partes de agua desionizada. Se prepara una premezcla de 7,25 partes de ácido eritórbico, 6,5 partes de DMEA, y 77 partes de agua desionizada. Esta premezcla inicial y 0,18 partes de HAMP-OL 4,5 % Iron se añaden al matraz. Los contenidos del matraz se calientan a 30 ºC. En un recipiente separado se prepara una premezcla de
30 monómero de 249 partes de estireno, 114 de BA, 107 partes de BMA, 178 partes de HEMA, 36 partes de IBMA, y 28 partes de GMA. Se prepara una tercera premezcla de 7,25 partes de TRIGONOX A-W70 y 82,2 partes de agua desionizada. Una vez que se han preparado todas las premezclas y el matraz está a 30 ºC, se ajusta el agitador a 240 rpm y se añade toda la premezcla de monómero. El recipiente de premezcla de monómero se aclara con 82
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CN101040016B (zh) | 2004-10-20 | 2011-08-03 | 威士伯采购公司 | 用于罐的涂料组合物和涂覆方法 |
US7644356B2 (en) * | 2005-06-10 | 2010-01-05 | Hewlett-Packard Development Company, L.P. | Constraint-based albuming of graphic elements |
ATE453508T1 (de) | 2005-08-11 | 2010-01-15 | Valspar Sourcing Inc | Beschichtungen frei von bisphenol-a und aromatischem glycidyl-ether |
BRPI0616274B1 (pt) | 2005-10-18 | 2017-12-05 | Valspar Sourcing, Inc. | Container understanding a metal food or drink container, method for preparing a container undertaking a metal food or drink container, and coating composition |
US20090061219A1 (en) * | 2007-08-28 | 2009-03-05 | Valspar Sourcing, Inc. | Composition for Coating Glass |
US8227027B2 (en) * | 2007-12-07 | 2012-07-24 | Presspart Gmbh & Co. Kg | Method for applying a polymer coating to an internal surface of a container |
BRPI0821167A2 (pt) * | 2007-12-07 | 2017-05-09 | Valspar Sourcing Inc | artigo revestido, e, método |
US9801865B2 (en) | 2008-09-24 | 2017-10-31 | The United States Of America As Represented By The Department Of Veteran Affairs | Materials and methods for diagnosis, prevention and/or treatment of stress disorders and conditions associated with abeta peptide aggregation |
US9394456B2 (en) | 2009-02-24 | 2016-07-19 | Akzo Nobel Coatings International B.V. | Latex emulsions and coating compositions formed from latex emulsions |
ES2655318T3 (es) * | 2009-02-24 | 2018-02-19 | Akzo Nobel Coatings International B.V. | Emulsiones de látex y composiciones de revestimiento formadas a partir de emulsiones de látex |
RU2539981C2 (ru) | 2009-03-05 | 2015-01-27 | Акцо Нобель Коатингс Интернэшнл Б.В. | Привитые акриловые сополимеры масляных полиолов с гидроксильными функциональными группами |
BRPI1014965B1 (pt) | 2009-04-09 | 2019-09-17 | Swimc Llc | Artigo, e, composição para revestimento |
CN102388080B (zh) | 2009-04-09 | 2014-09-24 | 威士伯采购公司 | 聚酯涂料组合物 |
WO2011009024A1 (en) * | 2009-07-17 | 2011-01-20 | Valspar Sourcing, Inc. | Coating compositions for cans and methods of coating |
EP3208289A1 (en) | 2009-07-17 | 2017-08-23 | Valspar Sourcing, Inc. | Coating composition and articles coated therewith |
CN102741319A (zh) | 2009-09-18 | 2012-10-17 | 威士伯采购公司 | 包含不饱和聚合物的涂料组合物 |
FR2953155B1 (fr) * | 2009-12-02 | 2011-12-30 | Peugeot Citroen Automobiles Sa | Procede de preparation de la caisse d'un vehicule automobile avant peinture |
MX2012011843A (es) | 2010-04-16 | 2012-11-12 | Valspar Sourcing Inc | Composiciones de revestimiento para envasar articulos y metodos de revestimiento. |
KR20170045394A (ko) * | 2010-08-30 | 2017-04-26 | 에이케이 스틸 프로퍼티즈 인코포레이티드 | 최종 형태가 스테인리스강인 아연 코팅 탄소강 |
WO2012036699A1 (en) | 2010-09-17 | 2012-03-22 | Empire Technology Development Llc | Partially hydrogenated bisphenol-a-based polymers as substitutes for bisphenol-a-based polymers |
CN106010157A (zh) * | 2010-10-15 | 2016-10-12 | 威士伯采购公司 | 用于金属基材的聚酯基涂料组合物 |
MY160309A (en) * | 2010-10-20 | 2017-02-28 | Valspar Sourcing Inc | Water-based coating system with improved adhesion to a wide range of coated and uncoated substrates including muffler grade stainless steel |
US9345656B2 (en) | 2010-12-02 | 2016-05-24 | Dsm Ip Assets B.V. | Acrylic polymer |
EP2658935B1 (en) | 2010-12-28 | 2016-03-09 | Akzo Nobel Coatings International B.V. | High acid large particle size latex emulsions, enhanced stabilization of high acid large particle size latex emulsions, and coating compositions formed therefrom |
EP2658933B1 (en) | 2010-12-29 | 2017-03-01 | Akzo Nobel Coatings International B.V. | Latex emulsions and coating compositions formed from latex emulsions |
US9617446B2 (en) | 2010-12-29 | 2017-04-11 | Akzo Nobel Coatings International B.V. | Adhesion promoter resin compositions and coating compositions having the adhesion promoter resin compositions |
PL3878912T3 (pl) * | 2011-02-07 | 2023-06-26 | Swimc Llc | Kompozycje powłokowe do pojemników i innych wyrobów i sposoby powlekania |
PL2505625T3 (pl) | 2011-03-31 | 2013-11-29 | Henkel Ag & Co Kgaa | Kompozycja lakierowa do wewnętrznych powierzchni puszek |
US8227561B1 (en) | 2011-05-02 | 2012-07-24 | Empire Technology Development Llc | Bisphenol-A replacement materials |
PL2705068T3 (pl) | 2011-05-02 | 2015-08-31 | Ppg Ind Ohio Inc | Kompozycje powłokowe zawierające 2,2’-bifenol |
US9670378B2 (en) | 2011-05-23 | 2017-06-06 | Ppg Industries Ohio, Inc. | Coating compositions with improved adhesion to containers |
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 |
US10442953B2 (en) | 2011-08-29 | 2019-10-15 | Ppg Industries Ohio, Inc. | Aqueous-based coating composition containing hydroxy-terminated polybutadiene |
HUE061699T2 (hu) | 2011-09-27 | 2023-08-28 | Crown Packaging Technology Inc | Eljárás dobozvég készítésére és dobozvég felhasználása játék játszására |
US9187221B2 (en) | 2011-09-27 | 2015-11-17 | Crown Packaging Technology, Inc. | Can ends having machine readable information |
EP2599844A1 (en) | 2011-12-02 | 2013-06-05 | PPG Industries Ohio Inc. | Coating composition for a food or beverage can |
US9260625B2 (en) | 2011-12-21 | 2016-02-16 | Akzo Nobel Coatings International B.V. | Water-based coating compositions |
ES2599253T3 (es) | 2011-12-21 | 2017-01-31 | Akzo Nobel Coatings International B.V. | Composiciones de revestimiento basadas en disolvente |
CN104024353A (zh) | 2011-12-28 | 2014-09-03 | 阿克佐诺贝尔国际涂料股份有限公司 | 用酚醛树脂固化的乙酰乙酸酯官能胶乳乳液和由其形成的涂料组合物 |
CN104244940B (zh) | 2012-02-16 | 2018-07-20 | 阿克索生物医药公司 | 减少胃肠道的弯曲杆菌定植 |
EP2814746B1 (en) * | 2012-02-17 | 2019-09-18 | Swimc Llc | Methods and materials for the functionalization of polymers and coatings including functionalized polymer |
CN104334474B (zh) | 2012-04-18 | 2017-10-31 | 威士伯采购公司 | 适合用于保护含金属基材包括食物和饮料包装体的低voc水基涂料组合物 |
KR102072593B1 (ko) * | 2012-06-19 | 2020-02-03 | 다우 글로벌 테크놀로지스 엘엘씨 | 수계 블렌드 조성물 및 그의 제조 방법 |
CN104540744B (zh) | 2012-08-09 | 2017-08-25 | 威士伯采购公司 | 容器涂层体系 |
AU2013299578A1 (en) | 2012-08-09 | 2015-02-19 | Valspar Sourcing, Inc. | Compositions for containers and other articles and methods of using same |
DE102012223356A1 (de) | 2012-12-17 | 2014-06-18 | Henkel Ag & Co. Kgaa | Verfahren zur Herstellung beschichteter Dosendeckel |
DE102012223355A1 (de) | 2012-12-17 | 2014-06-18 | Henkel Ag & Co. Kgaa | Hochvernetzende Lackformulierung für Doseninnenflächen |
US10358571B2 (en) | 2013-03-01 | 2019-07-23 | The Sherwin-Williams Company | Aqueous coating compositions including phenolic resin(s) |
ES2662851T3 (es) * | 2013-03-15 | 2018-04-10 | Akzo Nobel Coatings International B.V. | Composiciones de revestimiento formadas a partir de emulsiones de látex compuestas de copolímero de (poli)etileno y ácido (met)acrílico |
CN105339441B (zh) * | 2013-05-16 | 2019-01-08 | 可口可乐公司 | 用于食品和饮料包装的聚合物组合物和涂层 |
CN103275656B (zh) * | 2013-05-29 | 2015-07-08 | 北京化工大学 | 固化后具有结构胶性能的反应型压敏胶黏剂及其制备方法 |
US10308905B2 (en) | 2013-06-19 | 2019-06-04 | Isp Investments Llc | Method of removing phenols from a liquid |
CN105377703B (zh) | 2013-07-02 | 2017-09-08 | 威士伯采购公司 | 用于包装制品诸如食品和饮料容器的涂料组合物 |
MX2016000069A (es) * | 2013-07-02 | 2016-03-01 | Valspar Sourcing Inc | Composiciones de revestimiento para articulos de envasado tales como envases de alimentos y bebidas. |
US20150017359A1 (en) | 2013-07-11 | 2015-01-15 | Ppg Industries Ohio, Inc. | Coating compositions with improved adhesion to containers |
US10486865B2 (en) | 2013-10-02 | 2019-11-26 | The Sherwin-Williams Company | Removable closure and coating system |
CN105593131A (zh) | 2013-10-02 | 2016-05-18 | 威士伯采购公司 | 可移除封闭物和涂层体系 |
US10526277B2 (en) | 2013-10-17 | 2020-01-07 | Swimc Llc | Food or beverage containers coated with polymers of di(amido(alkyl)phenol) compounds |
US9464209B2 (en) | 2013-10-21 | 2016-10-11 | Ppg Industries Ohio, Inc. | Container coating compositions |
CN106133235B (zh) | 2014-04-07 | 2020-11-24 | 陶氏环球技术有限责任公司 | 用于碳纤维的施胶组合物 |
CN106536624B (zh) | 2014-04-14 | 2019-11-19 | 宣伟投资管理有限公司 | 制备用于容器和其它制品的组合物的方法以及使用所述组合物的方法 |
EP3146009A4 (en) | 2014-05-19 | 2017-12-06 | Valspar Sourcing, Inc. | Polyethers containing non-bisphenolic cyclic groups |
US10077352B2 (en) * | 2014-09-16 | 2018-09-18 | Eastman Chemical Company | Polymeric compositions with improved noise suppression |
EP3889159B1 (en) * | 2014-10-23 | 2024-06-05 | Inpria Corporation | Organometallic solution based high resolution patterning compositions |
US11981822B2 (en) | 2014-12-24 | 2024-05-14 | Swimc Llc | Crosslinked coating compositions for packaging articles such as food and beverage containers |
MX2017007830A (es) | 2014-12-24 | 2017-09-18 | Valspar Sourcing Inc | Composiciones de revestimiento libres de estireno para envasar articulos tales como envases de alimentos y bebidas. |
PL3741818T3 (pl) | 2014-12-24 | 2022-10-10 | Swimc Llc | Kompozycje powłokowe dla artykułów opakowaniowych, takich jak pojemniki na żywność i napoje |
US11059989B2 (en) * | 2017-06-30 | 2021-07-13 | Valspar Sourcing, Inc. | Crosslinked coating compositions for packaging articles such as food and beverage containers |
JP5968491B1 (ja) | 2015-04-20 | 2016-08-10 | 東洋製罐株式会社 | 液膜を有する構造体及びその製造方法 |
ES2750820T3 (es) | 2015-05-29 | 2020-03-27 | Ppg Ind Ohio Inc | Envase recubierto de un polímero de látex polimerizado en emulsión |
TWI614275B (zh) | 2015-11-03 | 2018-02-11 | Valspar Sourcing Inc | 用於製備聚合物的液體環氧樹脂組合物 |
WO2017106626A1 (en) * | 2015-12-16 | 2017-06-22 | Commonwealth Scientific And Industrial Research Organisation | Terpene derived coating composition |
CN108779383A (zh) | 2015-12-23 | 2018-11-09 | Swimc有限公司 | 用金属碱中和的表面活性剂制得的胶乳聚合物和包含此类聚合物的抗发白性涂料组合物 |
AR108133A1 (es) * | 2016-04-15 | 2018-07-18 | Valspar Sourcing Inc | Composiciones de revestimiento que contienen copolímeros libres de estireno |
FR3051395B1 (fr) * | 2016-05-20 | 2018-05-11 | Constellium Neuf-Brisach | Bande metalloplastique pour emballage alimentaire rigide et procede de fabrication |
EP3464478B1 (en) * | 2016-05-26 | 2020-12-09 | PPG Industries Ohio, Inc. | Packaging coated with an emulsion polymerized latex polymer |
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 |
EP3497023A4 (en) * | 2016-08-10 | 2020-07-29 | Swimc Llc | IMPROVING EDGE FORMATION AND EDGE HULL PERFORMANCE OF COIL COATINGS |
MX2019004562A (es) | 2016-10-19 | 2019-08-05 | Swimc Llc | Polimeros acrilicos y composiciones que contienen tales polimeros. |
CN110337474B (zh) * | 2016-12-21 | 2022-07-26 | 宣伟投资管理有限公司 | 含有反应性羰基的聚合物和含有所述聚合物的涂料组合物 |
US10800866B2 (en) | 2017-01-17 | 2020-10-13 | Behr Process Corporation | Self-healing resin |
CA3056987A1 (en) * | 2017-04-07 | 2018-10-11 | Akzo Nobel Coatings International B.V. | Coating compositions containing a hydroxyphenyl functional polymer and a latex polymer |
CN109423129B (zh) * | 2017-06-21 | 2020-08-28 | 广东华润涂料有限公司 | 适用于在三片罐上形成侧缝条或侧缝涂层的水性涂料组合物 |
WO2019040823A1 (en) | 2017-08-25 | 2019-02-28 | The Sherwin-Williams Company | MEMBRANE PROMOTERS AND COMPOSITIONS FOR CONTAINERS AND OTHER ARTICLES |
EP3676342A4 (en) | 2017-09-01 | 2021-07-07 | Swimc LLC | MULTI-LEVEL POLYMERS LATIZES, COATING COMPOSITIONS WITH SUCH LATIZES AND ARTICLES COATED WITH IT |
AU2018325278B2 (en) * | 2017-09-01 | 2023-11-30 | Swimc Llc | Multi-stage polymeric latexes, coating compositions containing such latexes, and articles coated therewith |
GB2581894B (en) * | 2017-10-16 | 2022-07-13 | Videojet Technologies Inc | A continuous inkjet ink composition |
MX2020005616A (es) | 2017-12-11 | 2020-09-22 | Sherwin Williams Co | Metodo para elaborar polimeros dispersables en agua y dispersos en agua. |
EP3498738A1 (en) | 2017-12-15 | 2019-06-19 | PPG Industries Ohio, Inc. | A coating composition |
CN108034341B (zh) * | 2017-12-28 | 2020-01-21 | 日照德联化工有限公司 | 一种基于有机氟不饱和聚酯树脂乳液的汽车漆及其制备方法 |
US10752799B2 (en) | 2018-02-07 | 2020-08-25 | Ppg Industries Ohio, Inc. | Self-curing coating compositions |
JP7232022B2 (ja) * | 2018-04-13 | 2023-03-02 | 東洋インキScホールディングス株式会社 | 水性塗料組成物、缶用部材、及び缶 |
US11390705B2 (en) | 2018-05-11 | 2022-07-19 | Carbon, Inc. | Reactive particulate materials useful for additive manufacturing |
EP3802714A4 (en) * | 2018-06-11 | 2022-03-23 | Swimc Llc | PACKAGING COATING WITH WATER-DISPERSABLE ACRYLIC BLOCK COPOLYMER |
CN108794703B (zh) * | 2018-06-27 | 2020-12-18 | 常州光辉化工有限公司 | 一种具有优良耐盐雾功能的聚丙烯酸酯防腐乳液的制备方法 |
CN113474421B (zh) * | 2018-12-13 | 2023-02-28 | Ppg工业俄亥俄公司 | 用作交联剂的聚羟基烷基酰胺材料 |
JP2022523790A (ja) * | 2019-03-01 | 2022-04-26 | ダウ グローバル テクノロジーズ エルエルシー | 粘着付与剤組成物 |
KR20220099551A (ko) | 2019-11-14 | 2022-07-13 | 에스더블유아이엠씨 엘엘씨 | 금속 패키징 분말 코팅 조성물, 코팅된 금속 기재, 및 방법 |
WO2021194722A1 (en) * | 2020-03-26 | 2021-09-30 | Michelman, Inc. | Low-blushing coating formulations and associated uses |
US11597791B2 (en) * | 2020-03-27 | 2023-03-07 | Ppg Industries Ohio, Inc. | Crosslinking material and uses thereof |
US20240101860A1 (en) * | 2021-01-29 | 2024-03-28 | Ppg Industries Ohio, Inc. | Coating composition |
JP2022148614A (ja) * | 2021-03-24 | 2022-10-06 | 富士フイルムビジネスイノベーション株式会社 | 複合樹脂粒子分散液の製造方法、感圧接着剤の製造方法、圧力応答性樹脂の製造方法、静電荷像現像用トナーの製造方法、及び、複合樹脂粒子分散液 |
WO2022246120A1 (en) | 2021-05-19 | 2022-11-24 | Swimc Llc | Methods of coating metal substrates and making metal packaging, coated metal substrates, metal packaging, and powder coating composition systems |
WO2023111186A1 (en) | 2021-12-16 | 2023-06-22 | Allnex Austria Gmbh | Coating composition |
Family Cites Families (353)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1234060A (en) | 1913-04-30 | 1917-07-17 | Gen Electric | Incandescent electric lamp. |
NL173809B (nl) * | 1951-11-17 | Rca Corp | Beeldopneeminrichting met kleurcodeerstrookfilterstelsel. | |
US3242123A (en) * | 1962-11-21 | 1966-03-22 | Union Carbide Corp | Glycidyl acrylate-styrene-ethyl acrylate-itaconic acid interpolymers |
GB1096912A (en) * | 1963-08-06 | 1967-12-29 | Ici Ltd | Synthetic polymers |
US3335119A (en) | 1963-08-08 | 1967-08-08 | Dal Mon Research Co | Fusible, convertible alkenyl aryl polymers |
DE1495745C3 (de) | 1963-09-19 | 1978-06-01 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung wäßriger, emulgatorfreier Polyurethan-Latices |
US3377406A (en) * | 1963-12-16 | 1968-04-09 | Shell Oil Co | Process of esterification of polyepoxides with ethylenically unsaturated monocarboxylic acids in the presence of onium salts of inorganic acids |
US3297621A (en) | 1965-01-04 | 1967-01-10 | Archer Daniels Midland Co | Two step polymerization of tetrapolymer |
NL137295C (es) | 1965-11-03 | |||
JPS4833015B1 (es) * | 1967-06-02 | 1973-10-11 | Nippon Paint Co Ltd | |
US3477990A (en) | 1967-12-07 | 1969-11-11 | Shell Oil Co | Process for reacting a phenol with an epoxy compound and resulting products |
US3547885A (en) | 1968-03-08 | 1970-12-15 | Sun Oil Co | Process for curing polyepoxides with anhydrides and phosphonium halide catalysts therefor |
CH515981A (de) | 1968-07-10 | 1971-11-30 | Bayer Ag | Lack |
US3568486A (en) | 1969-01-31 | 1971-03-09 | Montgomery H A Co | Preparation of metal for deforming operations |
BE757936A (fr) † | 1969-10-23 | 1971-04-01 | Bayer Ag | Procede de preparation de polymeres anioniques modifies en emulsion |
CA955347A (en) | 1970-06-29 | 1974-09-24 | Nippon Oils And Fats Company Limited | Paint compositions capable of being cured by irradiation of electron ray |
US3810859A (en) | 1970-07-22 | 1974-05-14 | Goodrich Co B F | Thickenable alkyl acrylate latices |
US3694407A (en) * | 1970-08-11 | 1972-09-26 | Shell Oil Co | Epoxy-containing condensates,their preparation and use |
US3948855A (en) * | 1971-09-16 | 1976-04-06 | The Dow Chemical Company | Process for reacting a phenol with a vicinal epoxy compound in the presence of phosphorus or carbon containing acid, ester or acid ester |
US3738862A (en) * | 1971-11-08 | 1973-06-12 | Shell Oil Co | Process for preparing reinforced laminates in situ with epoxy-polyhydric phenol condensates |
US3819567A (en) | 1971-12-03 | 1974-06-25 | Du Pont | Sealer composition of an acrylic-epoxy ester graft copolymer and an epoxy resin |
US3880793A (en) * | 1972-03-30 | 1975-04-29 | Kansai Paint Co Ltd | Emulsifiers for emulsion polymerization of vinyl monomers |
GB1421114A (en) | 1972-07-14 | 1976-01-14 | Canadian Ind | Thermosettable synthetic addition polymers |
US3862914A (en) | 1972-11-01 | 1975-01-28 | Mobil Oil Corp | Water-based coatings from polyepoxides and polycarboxylic acid monoanhydrides |
JPS5339387Y2 (es) | 1973-07-26 | 1978-09-25 | ||
GB1482969A (en) * | 1973-10-12 | 1977-08-17 | Kansai Paint Co Ltd | Non-flammable binder compositions |
US4303488A (en) | 1973-11-06 | 1981-12-01 | E. I. Du Pont De Nemours And Company | Electrocoating with water-borne coating composition made from epoxy resin, polymeric acid and tertiary amine |
US4247439A (en) | 1973-11-06 | 1981-01-27 | E. I. Du Pont De Nemours And Company | Water-borne coating composition made from epoxy resin, polymeric acid and tertiary amine |
US3945961A (en) | 1973-11-21 | 1976-03-23 | American Cyanamid Company | Novel cross-linking agents and their use in electrophoretic coating composition |
US3997694A (en) | 1973-12-12 | 1976-12-14 | E. I. Du Pont De Nemours And Company | Container coated with a ductile coating of an acrylic polymer having reactive sites and an epoxy resin |
US3943187A (en) * | 1973-12-12 | 1976-03-09 | E. I. Du Pont De Nemours And Company | Ductile coating composition of an acrylic polymer having reactive sites and an epoxy resin |
US4021396A (en) * | 1973-12-12 | 1977-05-03 | E. I. Du Pont De Nemours And Company | Aqueous coating composition of an acrylic polymer having reactive sites and an epoxy resin |
US4198330A (en) † | 1974-04-19 | 1980-04-15 | American Cyanamid Company | Polyurethane latices modified by a vinyl polymer |
CA1065988A (en) * | 1974-05-16 | 1979-11-06 | Roger M. Christenson | Water-based liners for beverage containers |
US3991216A (en) * | 1974-05-16 | 1976-11-09 | Ppg Industries, Inc. | Beverage containers coated with a water based liner |
US4033920A (en) * | 1974-06-14 | 1977-07-05 | Kansai Paint Company, Ltd. | Process for producing unsaturated resin emulsion |
US4076676A (en) * | 1975-02-04 | 1978-02-28 | E. I. Du Pont De Nemours And Company | Aqueous coating composition from aminoplast and reaction product of tertiary amine and polymer containing terminal epoxy groups |
US4105811A (en) | 1975-02-07 | 1978-08-08 | Polygulf Associates | Method of protectively coating metallic aluminum containing substrate |
JPS51146534A (en) | 1975-06-12 | 1976-12-16 | Asahi Chem Ind Co Ltd | Powder coating composition |
US4048141A (en) * | 1975-11-06 | 1977-09-13 | The Dow Chemical Company | Latent catalysts for promoting reaction of epoxides with phenols and/or carboxylic acids |
US4028294A (en) * | 1975-11-10 | 1977-06-07 | Mobil Oil Corporation | Epoxy modified acrylic latices and method of producing same |
US4064087A (en) | 1976-01-05 | 1977-12-20 | Ppg Industries, Inc. | Method for preparing polymers in aqueous medium |
GB1574721A (en) | 1976-03-03 | 1980-09-10 | Canadian Ind | Process for preparing aqueous copolymer emulsions |
JPS52108488A (en) * | 1976-03-08 | 1977-09-10 | Kao Corp | Preparation of liquid resin dispersions |
US4122052A (en) * | 1976-03-09 | 1978-10-24 | Kansai Paint Company, Limited | Emulsion composition |
US4148670A (en) | 1976-04-05 | 1979-04-10 | Amchem Products, Inc. | Coating solution for metal surface |
US4212781A (en) | 1977-04-18 | 1980-07-15 | Scm Corporation | Modified epoxy resins, processes for making and using same and substrates coated therewith |
US4308185A (en) | 1976-05-11 | 1981-12-29 | Scm Corporation | Graft polymer compositions of terminated epoxy resin, processes for making and using same, and substrates coated therewith |
US4147679A (en) | 1976-06-02 | 1979-04-03 | Ppg Industries, Inc. | Water-reduced urethane coating compositions |
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 (es) | 1976-09-09 | 1981-02-18 | ||
JPS5339387A (en) | 1976-09-24 | 1978-04-11 | Nippon Jiyunyaku Kk | Method of making aquaous emulsion polymer |
JPS5397083U (es) | 1977-01-11 | 1978-08-07 | ||
JPS5397083A (en) | 1977-02-03 | 1978-08-24 | Nippon Paint Co Ltd | Production of aqueous resin dispersion for coating |
US4136075A (en) | 1977-04-27 | 1979-01-23 | A. E. Staley Manufacturing Company | Acrylic copolymer coatings |
US4144155A (en) * | 1977-08-15 | 1979-03-13 | Japan Atomic Energy Research Institute | Radiation process for producing a reactive aqueous emulsion |
US4151143A (en) * | 1977-08-19 | 1979-04-24 | American Cyanamid Company | Surfactant-free polymer emulsion coating composition and method for preparing same |
US4482673A (en) | 1978-06-12 | 1984-11-13 | Scm Corporation | Aqueous coating composition comprising self-emulsifiable ester of epoxy and acid containing addition polymer and method of its preparation |
US4442246A (en) * | 1978-06-12 | 1984-04-10 | Scm Corporation | Aqueous coating composition comprising self-emulsifiable ester of epoxy and acid containing addition polymer |
US4191596A (en) | 1978-09-06 | 1980-03-04 | Union Carbide Corporation | Method and compositions for coating aluminum |
US4212776A (en) * | 1978-10-16 | 1980-07-15 | Mobil Oil Corporation | Self crosslinking water dispersible epoxy ester-acrylate polymers |
NZ191816A (en) | 1978-10-24 | 1981-03-16 | Canadian Ind | Preparation of aqueous copolymer emulsion |
US4174333A (en) | 1978-11-02 | 1979-11-13 | Ppg Industries, Inc. | Carboxylated amide polymers and coating compositions containing same |
DE2850872A1 (de) | 1978-11-24 | 1980-06-04 | Bayer Ag | Wasserverduennbare lackbindemittel fuer chemikalienfeste beschichtungen |
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 |
US4296011A (en) * | 1979-03-09 | 1981-10-20 | Desoto, Inc. | Epoxy ester copolymer aqueous dispersions |
US4247659A (en) * | 1979-03-09 | 1981-01-27 | Desoto, Inc. | Epoxy ester copolymer soluble in water with the aid of an amine |
US4285847A (en) * | 1979-04-11 | 1981-08-25 | Scm Corporation | Polymerization process and product |
US4304701A (en) | 1979-06-01 | 1981-12-08 | Ppg Industries, Inc. | Aqueous acrylic polymer dispersions |
US4413015A (en) | 1979-06-21 | 1983-11-01 | Mobil Oil Corporation | Storage stable water-dilutable acid adducted epoxy based coating for metal food contact surfaces |
US4329266A (en) | 1979-09-29 | 1982-05-11 | Kansai Paint Co., Ltd. | Water-dispersed coating composition comprising an acrylic graft polymer containing carboxyl groups, hydroxyl and/or amide groups |
US4294737A (en) * | 1979-12-28 | 1981-10-13 | Desoto, Inc. | Water soluble epoxy ester copolymers for interior can use |
US4289811A (en) * | 1980-02-21 | 1981-09-15 | Celanese Corporation | Stable aqueous dispersions of mixed resins and process for use as coating compositions |
US4404336A (en) * | 1980-05-27 | 1983-09-13 | Desoto, Inc. | Water soluble epoxy ester copolymers for interior can use |
JPS6039283B2 (ja) | 1980-06-12 | 1985-09-05 | 日立化成工業株式会社 | ポリブタジエン変性不飽和ポリエステルの製造法 |
US4347333A (en) | 1980-06-16 | 1982-08-31 | S. C. Johnson & Son, Inc. | Emulsion coating composition containing silicone and acrylic polymer |
US4337185A (en) * | 1980-06-23 | 1982-06-29 | The Dow Chemical Company | Process for making cationic structured particle latexes using reactive polymeric surfactants |
US4480058A (en) * | 1980-12-04 | 1984-10-30 | Scm Corporation | Aqueous epoxy ester emulsions |
US4443568A (en) * | 1981-10-26 | 1984-04-17 | Scm Corporation | Polymerization process and product |
US4423165A (en) | 1982-04-16 | 1983-12-27 | E. I. Du Pont De Nemours And Company | Water-borne coating composition made from epoxy resin, first polymeric acid, tertiary amine and second polymeric acid |
US4440897A (en) | 1982-06-01 | 1984-04-03 | Ppg Industries, Inc. | Process of making substantially external surfactant-free vinyl polymer emulsion products |
US4477609A (en) * | 1982-07-15 | 1984-10-16 | Inmont Corporation | Hydrosol coating compositions having improved stability |
FI832883A (fi) | 1982-08-12 | 1984-02-13 | Scm Corp | Vattenhaltig sjaelvhaerdbar polymerblandning |
US4499212A (en) | 1982-09-13 | 1985-02-12 | Scm Corporation | Thermosetting acrylic latexes |
US4425451A (en) * | 1982-09-29 | 1984-01-10 | Desoto, Inc. | Epoxy-phosphate aqueous dispersions |
US4461857A (en) * | 1982-09-29 | 1984-07-24 | Desoto, Inc. | Thermosetting aqueous coating compositions containing epoxy-phosphate dispersions |
US4546014A (en) * | 1982-12-16 | 1985-10-08 | Celanese Corporation | Water-swellable crosslinked polymeric microgel particles and aqueous dispersions of organic film-forming resins containing the same |
US4560714A (en) | 1982-12-16 | 1985-12-24 | Celanese Corporation | Water-swellable crosslinked polymeric microgel particles and aqueous dispersions of organic film-forming resins containing the same |
US4539348A (en) * | 1982-12-16 | 1985-09-03 | Celanese Corporation | Water-swellable crosslinked polymeric microgel particles and aqueous dispersions of organic film-forming resins containing the same |
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 |
US4446258A (en) * | 1982-12-30 | 1984-05-01 | Mobil Oil Corporation | Aqueous coating comprising dispersible epoxy resin-acid polymer ester and diluent polymer, and method of preparation |
US4444923A (en) * | 1982-12-30 | 1984-04-24 | Mobil Oil Corporation | Process for preparing aqueous coatings comprising dispersible epoxy resin-acid polymer ester |
US4476262A (en) * | 1982-12-30 | 1984-10-09 | Mobil Oil Corporation | Aqueous coatings comprising ionic polymer ester and diluent polymer with reduced monomer residue and method of preparation |
US4497946A (en) * | 1983-04-13 | 1985-02-05 | Desoto, Inc. | Epoxy phosphate-carboxyl copolymers and aqueous coatings containing the same |
US4487859A (en) | 1983-11-21 | 1984-12-11 | Scm Corporation | Self-curing water dispersed polymers |
US4487861A (en) | 1983-11-28 | 1984-12-11 | Scm Corporation | Aqueous polymeric blends |
US4503173A (en) | 1983-12-19 | 1985-03-05 | Scm Corporation | Self-curing water dispersed polymer blends |
US4629491A (en) | 1983-12-20 | 1986-12-16 | Allied Corporation | Oxidized sulfur derivatives of diaminophosphinyl compounds as urease inhibitors and urease inhibited urea based fertilizer compositions |
FR2557116B1 (fr) * | 1983-12-21 | 1988-07-22 | Inmont Corp | Compositions de revetement de resine epoxyphenolique acrylatee solubles dans l'eau |
US4600737A (en) * | 1983-12-21 | 1986-07-15 | Inmont Corporation | Water dilutable acrylated epoxy-phenolic coating compositions |
US4501831A (en) * | 1983-12-27 | 1985-02-26 | Chu Shaw C | Aqueous coating compositions and process for their preparation from epoxy acidic acrylic polymer and polyfunctional amine |
US4507425A (en) * | 1984-01-12 | 1985-03-26 | The B. F. Goodrich Company | Process for preparing stable poly(vinylidene halide) latices |
US4579888A (en) * | 1984-04-10 | 1986-04-01 | Toyo Ink Manufacturing Co., Ltd. | Aqueous resin dispersion |
US4585814A (en) * | 1984-05-14 | 1986-04-29 | Desoto, Inc. | Epoxy-maleate-phosphate copolymers |
US4572610A (en) | 1984-05-21 | 1986-02-25 | Desoto, Inc. | Optical fiber buffer coated with halogenated dihydroxy-terminated polybutadienes |
JPS6145059A (ja) | 1984-08-06 | 1986-03-04 | 株式会社アイジー技術研究所 | サイデイングボ−ド |
US5344858A (en) * | 1984-09-10 | 1994-09-06 | Ppg Industries, Inc. | Coating from phosphated epoxy and COOH-vinyl addition resins |
US4638020A (en) * | 1984-11-23 | 1987-01-20 | Ppg Industries, Inc. | Aqueous composition comprising a phosphated epoxy and non-self dispersible resin |
US4644030A (en) | 1985-02-01 | 1987-02-17 | Witco Corporation | Aqueous polyurethane - polyolefin compositions |
FR2577935B1 (fr) | 1985-02-26 | 1988-06-17 | Saint Gobain Vitrage | Couche adhesive a base de polyurethane et son utilisation dans les vitrages feuilletes |
US4623680A (en) | 1985-06-03 | 1986-11-18 | Celanese Corporation | Aqueous epoxy resin dispersions for can coating use |
DE3544337A1 (de) | 1985-12-14 | 1987-06-19 | Hoechst Ag | Polymerisatdispersionen, verfahren zu ihrer herstellung, sowie deren anwendung als bindemittel |
US4670500A (en) | 1985-12-20 | 1987-06-02 | Pennzoil Company | Surface coating composition |
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 |
DE3601560A1 (de) * | 1986-01-21 | 1987-07-23 | Herberts Gmbh | Waessriges, hitzehaertbares ueberzugsmittel, dessen verwendung und damit beschichtete gegenstaende |
US4703071A (en) * | 1986-01-27 | 1987-10-27 | The Glidden Company | Stabilized aqueous coatings containing zinc oxide |
US5093392A (en) * | 1986-05-05 | 1992-03-03 | The Glidden Company | Epoxy-acrylic graft polymers with aminoplast |
US5051470A (en) * | 1986-05-05 | 1991-09-24 | The Glidden Company | Epoxy-acrylic graft polymers |
US4683273A (en) * | 1986-05-27 | 1987-07-28 | The Glidden Company | Polyester and epoxy resin coating |
DE3627860A1 (de) * | 1986-08-16 | 1988-02-18 | Basf Lacke & Farben | Waessriges ueberzugsmittel, verfahren zu seiner herstellung sowie seine verwendung zur beschichtung von dosen |
AU590104B2 (en) | 1986-08-20 | 1989-10-26 | Glidden Company, The | Thermosetting emulsion polymers |
US4898911A (en) * | 1986-11-20 | 1990-02-06 | Kanegafuchi Kagaku Kogyo Kabushiki | Resin composition |
WO1988005455A1 (en) | 1987-01-27 | 1988-07-28 | Toyo Seikan Kaisha, Ltd. | Emulsion type water paint, process for its production, and process for applying same |
EP0294599A3 (de) * | 1987-06-12 | 1990-05-09 | F. Hoffmann-La Roche Ag | Tricyclische Pyridonderivate |
MX169357B (es) * | 1987-08-13 | 1993-09-30 | Valspar Corp | Composicion de revestimiento en composicion acuosa |
GB8721538D0 (en) † | 1987-09-14 | 1987-10-21 | Polyvinyl Chemie Holland Bv | Aqueous dispersions |
JPH0543830Y2 (es) | 1987-10-28 | 1993-11-05 | ||
AU2376188A (en) | 1987-10-30 | 1989-05-04 | Ppg Architectural Finishes, Inc. | Alkyd based waterborne deck stain composition |
US4871810A (en) * | 1987-11-13 | 1989-10-03 | E. I. Du Pont De Nemours And Company | Composition comprising melt blended product of thermoplastic resin and two ethylene copolymers containing coreactive groups |
US5087603A (en) | 1987-12-14 | 1992-02-11 | Nippon Shokubai Co., Ltd. | Heat-sensitive recording paper having an overcoat layer formed from an aqueous crosslinkable resin dispersion |
US5087842A (en) | 1988-01-06 | 1992-02-11 | Digital Equipment Corporation | Delay circuit having one of a plurality of delay lines which may be selected to provide an operation of a ring oscillator |
US4894397A (en) | 1988-04-21 | 1990-01-16 | S. C. Johnson & Son, Inc. | Stable emulsion polymers and methods of preparing same |
FR2638466B1 (fr) | 1988-11-03 | 1993-05-07 | Atochem | Procede pour revetir des substrats metalliques a l'aide d'un primaire en poudre et d'un revetement superficiel applique par trempage, compositions de primaire en poudre utilisees et materiaux composites obtenus |
US4906684A (en) | 1988-12-09 | 1990-03-06 | Rtz Chemicals, Ltd. | Ambient temperature curing polymer compositions containing acetoacetoxyethyl methacrylate, glycidyl methacrylate and a polymerizable acid |
AU613550B2 (en) | 1989-01-17 | 1991-08-01 | Ppg Industries, Inc. | Use of mixed polymeric surfactants for improved properties |
US5096992A (en) | 1989-03-20 | 1992-03-17 | Reeves Brothers, Inc. | Use of modified diisocyanates for preparing linear thermoplastic polyurethane elastomers having improved properties |
US4948834A (en) * | 1989-03-27 | 1990-08-14 | Ppg Industries, Inc. | Vinyl chloride-olefin copolymers having good color stability and flexibility for container coatings |
EP0394589B1 (en) | 1989-04-25 | 1994-03-09 | Toyo Ink Manufacturing Co., Ltd. | Aqueous coating composition for cans |
US4946911A (en) * | 1989-05-22 | 1990-08-07 | The Dow Chemical Company | Epoxy resin and water borne coatings therefrom |
AU5383290A (en) * | 1989-06-12 | 1990-12-13 | Ppg Industries, Inc. | Vinyl chloride latex composition having improved stability and durability properties |
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 |
US5116888A (en) * | 1989-09-22 | 1992-05-26 | The Glidden Company | Epoxy-acrylic graft copolymers with phosphonium cocatalysts carbon-graft |
US4963602A (en) * | 1989-11-13 | 1990-10-16 | Hi-Tek Polymers, Inc. | Aqueous epoxy resin-acrylic resin coating compositions containing also phenoxy, novolac and resole resin combination |
US5196481A (en) * | 1989-11-13 | 1993-03-23 | Glidden Company | Acrylic terpolymer surfactant for aqueous dispersed epoxy/acrylic binders |
US5201436A (en) * | 1989-11-13 | 1993-04-13 | The Glidden Company | Can coating of epoxy resin, acrylic copolymer and acrylic surfactant |
US5244960A (en) | 1990-04-02 | 1993-09-14 | Ppg Industries, Inc. | Thermosetting waterborne coating compositions prepared from aqueous emulsion polymers |
US5166272A (en) | 1990-04-02 | 1992-11-24 | Ppg Industries, Inc. | Emulsion polymers and coating compositions prepared therefrom |
US5212241A (en) * | 1990-05-25 | 1993-05-18 | The Glidden Company | Glycidyl-epoxy-acrylic copolymers |
US5157078A (en) * | 1990-05-25 | 1992-10-20 | The Glidden Company | Glycidyl-epoxy-acrylic copolymers |
US5082742A (en) | 1990-09-24 | 1992-01-21 | Monsanto Company | Composite of a styrenic polymer adhered to a polyolefin |
US5043380A (en) | 1990-10-29 | 1991-08-27 | The Dexter Corporation | Metal container coating compositions comprising an acrylic polymer latex, melamine formaldehyde resin and an phenol formaldehyde resin |
US5166289A (en) | 1990-12-19 | 1992-11-24 | Exxon Chemical Patents Inc. | Thermoset coating composition having improved hardness |
US5196055A (en) | 1991-01-23 | 1993-03-23 | The Sherwin-Williams Company | VOC compliant pretreatment primers |
US5500463A (en) * | 1991-03-11 | 1996-03-19 | Nippon Paint Co., Ltd. | Aqueous resin composition and method for forming coating film on can body |
US5177129A (en) * | 1991-04-22 | 1993-01-05 | The Valspar Corporation | Interior can coating compositions containing cyclodextrins |
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 |
JP2808999B2 (ja) | 1991-07-11 | 1998-10-08 | 東洋インキ製造株式会社 | 水性塗料組成物 |
DE4131706C2 (de) * | 1991-09-24 | 1994-10-20 | Basf Lacke & Farben | Verfahren zur Herstellung einer wäßrigen Beschichtungszusammensetzung, wäßrige Beschichtungszusammensetzungen sowie deren Verwendung zur Beschichtung von Emballagen |
US5264469A (en) | 1991-10-01 | 1993-11-23 | The Valspar Corporation | Aqueous epoxy resin-based coating compositions useful for coating metal containers |
WO1993008154A1 (en) | 1991-10-18 | 1993-04-29 | Akzo Nobel N.V. | SYNTHESIS OF α,φ-BIS(p-HYDROXYBENZOYLOXY) ALKANE |
GB9122594D0 (en) * | 1991-10-24 | 1991-12-04 | Ici Plc | Plastisol compositions |
US5252669A (en) * | 1991-12-19 | 1993-10-12 | Ppg Industries, Inc. | Grafted, thermoplastic, waterborne polymer and coating composition |
AU658736B2 (en) | 1992-05-26 | 1995-04-27 | Nippon Paint Co., Ltd. | Coating composition process for forming a coating composite and a multi-layer coating composite |
US5252637A (en) * | 1992-06-12 | 1993-10-12 | The Glidden Company | Low VOC, high molecular weight epoxy emulsion coatings |
JP2752862B2 (ja) | 1992-08-28 | 1998-05-18 | 日本エヌエスシー株式会社 | 一成分系水性プライマー組成物 |
JP2886007B2 (ja) | 1992-10-23 | 1999-04-26 | 鐘淵化学工業株式会社 | 塗料用硬化性組成物 |
AU5733594A (en) | 1992-11-30 | 1994-06-22 | Bulk Chemicals, Inc. | A method and composition for treating metal surfaces |
JP3503646B2 (ja) | 1993-01-21 | 2004-03-08 | 日本ゼオン株式会社 | アルカリ可溶性オリゴマーの水性分散液及びこれを用いて水性重合体分散液を製造する方法 |
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 |
US5387625A (en) * | 1993-05-18 | 1995-02-07 | The Dexter Corporation | Waterborne coating composition for metal containers |
US5506328A (en) | 1993-05-24 | 1996-04-09 | Olin Corporation | Low VOC, moisture curable, two-component coating compositions based on organic polyisocyanates |
US5290828A (en) | 1993-06-11 | 1994-03-01 | The Glidden Company | Aqueous dispersed acrylic grafted epoxy polyester protective coatings |
US5726244A (en) * | 1995-08-10 | 1998-03-10 | Basf Corporation | Aqueous coating compositions for environmental etch resistant coatings |
US5504145A (en) | 1993-08-31 | 1996-04-02 | The Thompson Minwax Company | Water-dispersible poly(urethane-urea) compositions |
JP3804993B2 (ja) * | 1993-09-20 | 2006-08-02 | キヤノン株式会社 | インクジェット記録方法、係る方法に用いる記録液及び機器 |
US5714539A (en) * | 1993-10-04 | 1998-02-03 | Ppg Industries, Inc. | Polymeric surfactant and latex made therefrom |
JP3503647B2 (ja) | 1993-10-19 | 2004-03-08 | 日本ゼオン株式会社 | 水性塗被用組成物 |
WO1995017450A1 (de) | 1993-12-23 | 1995-06-29 | Vianova Resins Aktiengesellschaft | Verfahren zur herstellung von wasserverdünnbaren lackbindemitteln auf der basis von acrylatcopolymerisaten und deren verwendung |
JPH07188353A (ja) | 1993-12-27 | 1995-07-25 | Taisei Kako Kk | 水性アクリル−ウレタン複合体にもとづく常温硬化性水性樹脂組成物及びこれを用いたコーティング剤又はインキ |
EP0669382A1 (en) | 1994-02-28 | 1995-08-30 | Dsm N.V. | Use of a polyester in the preparation of coatings for the interior of can ends |
US5723555A (en) * | 1994-03-29 | 1998-03-03 | Ppg Industries, Inc. | Vinyl resins containing alkoxyacrylamide-polyol reaction products and use in epoxy resin blends for coatings |
US5428084A (en) * | 1994-03-29 | 1995-06-27 | Ppg Industries, Inc. | Defunctionalized epoxy resins useful in coatings |
US5464885A (en) | 1994-04-04 | 1995-11-07 | The Glidden Company | Low VOC, aqueous dispersed, epoxy-ester acrylic graft coatings |
US6140386A (en) | 1994-04-19 | 2000-10-31 | Vanderhoff; John W. | Aqueous coating compositions, methods for making same and uses thereof |
GB9408725D0 (en) | 1994-05-03 | 1994-06-22 | Zeneca Resins Bv | Production of aqueous polymer compositions |
GB9408748D0 (en) | 1994-05-03 | 1994-06-22 | Zeneca Resins Bv | Production of aqueous polymer compositions |
US5576361A (en) | 1995-04-20 | 1996-11-19 | The Glidden Company | Zero VOC, aqueous dispersed, polyester modified acrylic-epoxy microgel polymers |
US5508325A (en) * | 1995-01-19 | 1996-04-16 | The Glidden Company | Aqueous dispersed, acrylic grafted epoxy microgel protective coatings |
US5554671A (en) * | 1994-05-25 | 1996-09-10 | The Glidden Company | Low VOC, aqueous dispersed acrylic epoxy microgels |
JP3358873B2 (ja) | 1994-06-28 | 2002-12-24 | 日本エヌエスシー株式会社 | プライマー用水溶液 |
JP3412919B2 (ja) | 1994-07-13 | 2003-06-03 | 関西ペイント株式会社 | 缶外面用水性塗料 |
US5521246A (en) | 1994-07-25 | 1996-05-28 | Air Products And Chemicals, Inc. | Low temperature self-crosslinking aqueous urethane-vinyl polymers for coating applications |
US5612415A (en) | 1994-07-28 | 1997-03-18 | Basf Corporation | Process for coating a substrate with coatings including high Tg acrylic polymers and coated article obtained thereby |
US5623085A (en) | 1994-09-23 | 1997-04-22 | Rohm And Haas Company | Method for reducing microfoam in a spray-applied waterborne composition |
US5527840B1 (en) * | 1994-10-04 | 1999-08-10 | Valspar Corp | Aqueous coating composition |
EP0794970B1 (de) * | 1994-11-29 | 1998-09-09 | Vianova Resins Aktiengesellschaft | Verfahren zur zweistufigen herstellung von wässrigen, selbstvernetzenden copolymerisatdispersionen und deren verwendung für lacke |
AUPN023294A0 (en) | 1994-12-22 | 1995-01-27 | Commonwealth Scientific And Industrial Research Organisation | Polymerisable monomers and polymers |
JP3392247B2 (ja) * | 1995-02-02 | 2003-03-31 | 関西ペイント株式会社 | 水性被覆組成物 |
US5869590A (en) | 1995-04-12 | 1999-02-09 | Eastman Chemical Company | Waterborne polymers having pendant allyl groups |
US5576063A (en) | 1995-04-21 | 1996-11-19 | Basf Corporation | Multiple layer coating method |
US5532297A (en) * | 1995-05-26 | 1996-07-02 | The Glidden Company | Divinyl benzene modified, aqueous dispersed, acrylic graft coatings |
EP0747442B1 (en) † | 1995-06-07 | 2003-09-03 | National Starch and Chemical Investment Holding Corporation | Modified aqueous polyurethane dispersions and methods for making same |
JP3817761B2 (ja) * | 1995-09-18 | 2006-09-06 | 関西ペイント株式会社 | 水性被覆組成物 |
NZ299466A (en) | 1995-10-05 | 1998-01-26 | Rohm & Haas | Coating composition comprising a polymer from acetoacetate-functional monomer |
JP3060091B2 (ja) * | 1995-11-20 | 2000-07-04 | 三洋化成工業株式会社 | 光ディスク用オーバーコート組成物 |
US5830952A (en) * | 1996-02-22 | 1998-11-03 | The Dexter Corporation | Water-dispersible polymer and coating composition containing the same |
JPH09227824A (ja) | 1996-02-23 | 1997-09-02 | Kansai Paint Co Ltd | 水性塗料組成物 |
US5907012A (en) | 1996-04-08 | 1999-05-25 | H.B. Fuller Licensing & Financing, Inc. | Water-based polyurethane-urea laminating adhesives and primers |
TW377370B (en) | 1996-04-12 | 1999-12-21 | Du Pont | Waterborne fluoropolymer solutions for treating hard surfaces |
US5672653A (en) | 1996-05-13 | 1997-09-30 | Elf Atochem North America, Inc. | Anionic waterborne polyurethane dispersions |
US5686511A (en) | 1996-06-28 | 1997-11-11 | The Valspar Corporation | Esterifying epoxy resin with carboxyl polymer and quenching |
US5693723A (en) | 1996-07-01 | 1997-12-02 | Basf Corporation | Low voc curable coating composition utilizing carbamate-functional compound |
DE69636600T2 (de) * | 1996-08-12 | 2007-08-16 | Toyo Ink Mfg. Co., Ltd. | Wässrige dispersionszusammensetzung |
DE19633769A1 (de) * | 1996-08-22 | 1998-02-26 | Basf Lacke & Farben | Dispersion zur Herstellung eines elektrophoretisch abscheidbaren Tauchlackes |
US5962620A (en) | 1996-08-26 | 1999-10-05 | Tyndale Plains-Hunter, Ltd. | Hydrophicic and hydrophobic polyether polyurethanes and uses therefor |
US5993972A (en) | 1996-08-26 | 1999-11-30 | Tyndale Plains-Hunter, Ltd. | Hydrophilic and hydrophobic polyether polyurethanes and uses therefor |
US6048924A (en) | 1996-09-10 | 2000-04-11 | Dainippon Ink And Chemicals, Inc. | Aqueous resin composition and aqueous paint |
US6083585A (en) | 1996-09-23 | 2000-07-04 | Bp Amoco Corporation | Oxygen scavenging condensation copolymers for bottles and packaging articles |
US5763012A (en) | 1996-10-16 | 1998-06-09 | Basf Aktiengesellschaft | Coating of substrates |
DE19645663A1 (de) | 1996-11-06 | 1998-05-07 | Bayer Ag | Biologisch abbaubare und kompostierbare Formkörper |
JP2837142B2 (ja) | 1996-11-14 | 1998-12-14 | 大成化工株式会社 | 水性アクリル−ウレタン複合体である常温硬化性水性樹脂組成物及びこれを用いたコーティング剤又はインキ |
JP3155480B2 (ja) | 1996-12-05 | 2001-04-09 | 日本エヌエスシー株式会社 | 一液常温架橋型エマルジョン組成物およびその製法 |
JPH10273621A (ja) * | 1997-01-28 | 1998-10-13 | Nkk Corp | プレコート鋼板用塗料組成物並びにプレコート鋼板及びその製造方法 |
US5733970A (en) * | 1997-01-28 | 1998-03-31 | The Glidden Company | Aqueous dispersed, epoxy crosslinked maleated oil microgel polymers for protective coatings |
GB9708823D0 (en) * | 1997-05-01 | 1997-06-25 | Glidden Co | Aqueous dispersed,latex polymer modified acrylic-epoxy copolymer,microgel polymers for protective coatings |
US6008273A (en) | 1997-05-09 | 1999-12-28 | The Dexter Corporation | Waterborne coating compositions for metal containers |
EP0881243B1 (en) | 1997-05-19 | 2004-11-17 | Nisshinbo Industries, Inc. | Curing agent for powder coatings, powder coating composition comprising said curing agent, and powder coating film |
US5976615A (en) | 1997-07-09 | 1999-11-02 | Basf Corporation | Carbamate curable coating composition and method for improved adhesion |
US5942563A (en) * | 1997-07-18 | 1999-08-24 | The Glidden Company | Aqueous dispersed acrylic-epoxy, branched epoxy protective coatings |
US6136927A (en) * | 1997-09-24 | 2000-10-24 | Ppg Industries Ohio, Inc. | Phosphatized amine chain-extended epoxy polymeric compounds |
JP3726452B2 (ja) * | 1997-10-28 | 2005-12-14 | 松下電工株式会社 | 積層体成形用サーマルバリア |
US6150429A (en) | 1997-10-30 | 2000-11-21 | Foster-Miller, Inc. | Polyester/vinyl dioxolane based coating compositions |
AU751366B2 (en) | 1997-11-17 | 2002-08-15 | Delta Airlines, Inc. | Surface treatments for articles and vehicles |
US6262217B1 (en) | 1997-12-15 | 2001-07-17 | Lord Corporation | Polyurethane compositions |
US6087417A (en) * | 1998-01-16 | 2000-07-11 | The Valspar Corporation | Epoxy resin/acid/tertiary amine reaction product with reactive diluent |
US6054208A (en) | 1998-01-16 | 2000-04-25 | Avery Dennison Corporation | Film forming mixtures, image bearing films and image bearing retroreflective sheeting |
DE19805421C1 (de) | 1998-02-11 | 1999-06-02 | Basf Coatings Ag | Beschichtungsmittel und dessen Verwendung sowie Verfahren zu dessen Herstellung |
DE69924974T2 (de) | 1998-02-18 | 2006-02-23 | PPG Industries Ohio, Inc., Cleveland | Mehrkomponentige zusammengesetzte beschichtungsmasse und beschichtetes substrat |
FR2776662B1 (fr) | 1998-03-25 | 2000-05-05 | Atochem Elf Sa | Dispersions aqueuses de polyurethane et leur procede de preparation |
GB9807213D0 (en) | 1998-04-04 | 1998-06-03 | Ici Ltd | Aqueous coating composition |
US6126999A (en) | 1998-04-13 | 2000-10-03 | Tomasino; Randolf R. | Urethane-acrylic rubber coating and method of forming a vehicle bed liner |
IT1301690B1 (it) | 1998-06-11 | 2000-07-07 | Sinco Ricerche Spa | Miscele di resine poliestere aventi elevate proprieta' di barriera aigas. |
US6365673B1 (en) | 1998-06-22 | 2002-04-02 | E. I. Du Pont De Nemours And Company | Low viscosity imine reactive diluents and coating compositions made therefrom |
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 |
WO2000011094A1 (fr) | 1998-08-20 | 2000-03-02 | Asahi Glass Company Ltd. | Dispersion aqueuse de copolymere fluore et composition pour substance d'enduction a base d'eau |
CA2283373A1 (en) | 1998-09-25 | 2000-03-25 | Akzo Nobel Nv | Aqueous cross-linkable polymer composition for use in coatings |
US6251973B1 (en) | 1998-11-23 | 2001-06-26 | Akzo Nobel N.V. | Coatings and coating compositions of a reactive group-containing polymer, a hydrazide and a silane |
US6458468B1 (en) | 1999-01-28 | 2002-10-01 | Eastman Chemical Company | Photocurable coatings for polyester articles |
US7303797B1 (en) | 1999-02-16 | 2007-12-04 | E.I. Du Pont De Nemours And Company | Gas barrier coating system for polymeric films and rigid containers |
US6359062B1 (en) * | 1999-03-02 | 2002-03-19 | The Valspar Corporation | Coating compositions |
DE19912794A1 (de) | 1999-03-16 | 2000-09-21 | Grace W R & Co | BADGE-freie Dosenbeschichtung |
US6420040B1 (en) | 1999-04-30 | 2002-07-16 | The Valspar Corporation | Coating composition for metal substrates |
US6635735B1 (en) | 1999-06-16 | 2003-10-21 | Nihon Yamamura Glass Co., Ltd. | Coating composition |
AU771282B2 (en) | 1999-07-30 | 2004-03-18 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
US6300422B1 (en) | 1999-08-25 | 2001-10-09 | Lilly Industries, Inc. | Tris(alkoxycarbonylamino)triazine crosslinked waterborne coating system |
US6114430A (en) | 1999-08-25 | 2000-09-05 | H.B. Fuller Licensing & Financing, Inc. | Aqueous paint compositions comprising polyether amides |
EP1081199A1 (en) | 1999-09-06 | 2001-03-07 | Dsm N.V. | Composition |
US6194513B1 (en) | 1999-09-22 | 2001-02-27 | Olin Corporation | Tintable water-based coating composition |
US6255366B1 (en) * | 1999-10-01 | 2001-07-03 | Eastman Chemical Company | Sulfopolymers as emulsion stabilizers with improved coagulum level |
AU775474B2 (en) | 1999-10-04 | 2004-08-05 | Daikin Industries, Ltd. | Highly weathering-resistant powder coating composition |
JP2001146572A (ja) | 1999-11-19 | 2001-05-29 | Jsr Corp | コーティング組成物およびそれより得られる硬化膜 |
GB9927432D0 (en) | 1999-11-20 | 2000-01-19 | Avecia Bv | Aqueous polymer emulsions |
DE10010405A1 (de) | 2000-03-03 | 2001-09-13 | Basf Coatings Ag | Wäßrige (Meth)Acrylatcopolymerisat-Dispersionen, Verfahren zu ihrer Herstellung und ihre Verwendung |
KR20010100849A (ko) * | 2000-03-27 | 2001-11-14 | 사사키 요시오 | 수성 도료용 수지 조성물 및 수성 도료 조성물 |
WO2001092366A1 (en) | 2000-05-25 | 2001-12-06 | Battelle Memorial Institute | Reversible crosslinked polymers, benzyl crosslinkers and method |
DE10033851A1 (de) | 2000-07-12 | 2002-01-24 | Solutia Austria Gmbh Werndorf | Wässrige Polyurethandispersionen enthaltend Polybutadien-Bausteine |
US7459167B1 (en) | 2000-07-27 | 2008-12-02 | 3M Innovative Properties Company | Biocidal polyurethane compositions and methods of use |
US6514619B2 (en) * | 2000-08-30 | 2003-02-04 | Dainippon Ink And Chemicals, Inc. | Aqueous resin composition and coated metal material having cured coating of the same |
GB0023514D0 (en) | 2000-09-26 | 2000-11-08 | Ici Plc | Aqueous dispersion of addition polymer particles |
JP2002129095A (ja) | 2000-10-20 | 2002-05-09 | Kansai Paint Co Ltd | 水性被覆組成物 |
US6465559B1 (en) | 2000-10-30 | 2002-10-15 | Crompton Corporation | Sizing composition |
US6339125B1 (en) | 2000-10-30 | 2002-01-15 | Crompton Corporation | Cationic polyurethane dispersion and composition containing same |
JP2002138245A (ja) * | 2000-11-01 | 2002-05-14 | Kansai Paint Co Ltd | 水性被覆組成物 |
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 |
US6800717B2 (en) | 2001-05-23 | 2004-10-05 | Air Products And Chemicals, Inc. | Acid catalyzed copolymerization of water and epoxy resin and uses thereof |
US6689200B2 (en) | 2001-07-25 | 2004-02-10 | The Sherwin-Williams Company | Film-forming water-based water repellent coating compositions |
US7063895B2 (en) | 2001-08-01 | 2006-06-20 | National Starch And Chemical Investment Holding Corporation | Hydrophobically modified solution polymers and their use in surface protecting formulations |
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 |
US6930143B2 (en) | 2001-11-01 | 2005-08-16 | Arco Chemical Technology, L.P. | Acrylic latex composition |
US6872789B2 (en) | 2001-11-07 | 2005-03-29 | Akzo Nobel N.V. | Cross-linkable polymer composition |
AU2003217377A1 (en) | 2002-02-12 | 2003-09-04 | Valspar Sourcing, Inc. | Method of coating a packaging container using crosslinkable polyester-polyurethane |
US6784248B2 (en) | 2002-02-15 | 2004-08-31 | Ppg Industries Ohio, Inc. | Thermosetting compositions containing alternating copolymers of isobutylene type monomers |
EP1485436B1 (en) * | 2002-03-08 | 2007-07-04 | Valspar Sourcing, Inc. | Coatings having low volatile organic compound content |
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 |
JP4228585B2 (ja) * | 2002-05-01 | 2009-02-25 | 東洋製罐株式会社 | 金属包装体用水性塗料及びその塗料を用いた金属包装体 |
US6790904B2 (en) | 2002-06-03 | 2004-09-14 | Ppg Industries Ohio, Inc. | Liquid coating of film-forming resin and particles chemically modified to lower surface tension |
US20030232386A1 (en) | 2002-06-17 | 2003-12-18 | Shah Dinesh O. | Assay conjugate and uses thereof |
JP4165130B2 (ja) | 2002-06-24 | 2008-10-15 | 東洋インキ製造株式会社 | 塗料組成物 |
EP2128209B1 (en) | 2002-08-01 | 2015-12-23 | Valspar Sourcing, Inc. | Coating composition for metal substrates |
GB0218125D0 (en) | 2002-08-05 | 2002-09-11 | Mckeown Colm | A robot harvesting system |
US7745508B2 (en) | 2002-08-30 | 2010-06-29 | Ppg Industries Ohio, Inc. | Compositions and methods for coating food cans |
DE10252627A1 (de) | 2002-11-11 | 2004-05-27 | Surface Specialties Germany Gmbh & Co. Kg | Bindemittel und ihre Anwendung als Beschichtungsmaterial für die Beschichtung von Metallbehältern |
US7268176B2 (en) | 2002-12-12 | 2007-09-11 | Ppg Industries Ohio, Inc. | Additives for imparting mar and scratch resistance and compositions comprising the same |
GB2397578B (en) | 2002-12-17 | 2004-12-08 | Ici Plc | Aqueous dispersions of polyurethane-addition polymer hybrid particles especially for use in coating compositions |
JP3865693B2 (ja) | 2002-12-26 | 2007-01-10 | 日本ペイント株式会社 | アルミニウム−亜鉛合金メッキ鋼板処理用水性樹脂組成物、被覆方法及びアルミニウム−亜鉛合金メッキ鋼板 |
US6831136B2 (en) | 2003-01-14 | 2004-12-14 | Sartomer Technology Company, Inc. | Amino-terminated polybutadienes |
US6806314B2 (en) | 2003-02-03 | 2004-10-19 | Ppg Industries Ohio, Inc. | Coating of Hydroxy-functional polymer(s), crosslinker, and 1,3- and 1,4-cyclohexane dimethanols |
DE10308103A1 (de) | 2003-02-26 | 2004-09-09 | Bayer Ag | Wässrige Beschichtungsmittel auf Basis von PUR-PAC-Hybriddispersionen |
BRPI0408909B1 (pt) | 2003-04-02 | 2016-08-02 | Valspar Sourcing Inc | método para formar uma dispersão, composição, método para revestir um artigo, e, artigo |
WO2004099261A1 (en) | 2003-05-06 | 2004-11-18 | Nuplex Resins B.V. | Emulsion polymerization process, polymer dispersion and film-forming composition |
US7728068B2 (en) | 2003-06-12 | 2010-06-01 | Valspar Sourcing, Inc. | Coating compositions containing reactive diluents and methods |
CN1234060C (zh) | 2003-06-12 | 2005-12-28 | 凌阳科技股份有限公司 | 一种音乐档案产生及播放的方法 |
DE10332723A1 (de) | 2003-07-18 | 2005-02-03 | Degussa Ag | Lösungsmittelhaltige Beschichtungszusammensetzungen |
JP4591654B2 (ja) | 2003-08-08 | 2010-12-01 | 東洋インキ製造株式会社 | 水性塗料組成物及び該塗料組成物の製造方法 |
JP2007502350A (ja) | 2003-08-13 | 2007-02-08 | ヴァルスパー ソーシング,インク. | 水系ポリウレタン‐ポリエチレン系組成物 |
JP4344673B2 (ja) | 2003-10-15 | 2009-10-14 | フタムラ化学株式会社 | ガスバリアフィルム |
WO2005037923A1 (ja) | 2003-10-15 | 2005-04-28 | Mitsui Takeda Chemicals, Inc. | ガスバリア性水性樹脂組成物及びそれを用いた積層フィルム |
JP4661046B2 (ja) | 2003-12-19 | 2011-03-30 | 東洋インキ製造株式会社 | ポリマーエマルジョン含有水性塗料組成物 |
US7867555B2 (en) | 2004-02-13 | 2011-01-11 | Valspar Sourcing Inc. | Dispersion-coated powder coloring system |
US7375174B2 (en) | 2004-03-04 | 2008-05-20 | Basf Corporation | Acrylic composition and a curable coating composition including the same |
WO2005087875A1 (en) | 2004-03-05 | 2005-09-22 | The Sherwin-Williams Company | High energy curable coatings comprising thermoplastic polymers |
EP1584638A1 (en) | 2004-03-29 | 2005-10-12 | Imperial Chemical Industries Plc. | Coating composition based on modified epoxy resins |
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 |
JP4621460B2 (ja) | 2004-09-07 | 2011-01-26 | 出光サートマー株式会社 | 液状重合体組成物 |
CN101040016B (zh) † | 2004-10-20 | 2011-08-03 | 威士伯采购公司 | 用于罐的涂料组合物和涂覆方法 |
US7479519B2 (en) | 2004-10-27 | 2009-01-20 | Mallard Creek Polymers, Inc. | Curable urethane polymer adhesives and coatings |
US7666951B2 (en) | 2005-02-24 | 2010-02-23 | Ppg Industries Ohio, Inc. | Coating compositions that include a polyester polyol, related coated substrates, multi-layer coating and methods |
US7919146B2 (en) | 2005-03-17 | 2011-04-05 | Dsm Ip Assets B.V. | Aqueous polyurethane compositions |
WO2006125118A2 (en) | 2005-05-13 | 2006-11-23 | The Regents Of The University Of California | Vertical axis wind turbines |
US7475786B2 (en) | 2005-08-03 | 2009-01-13 | Ppg Industries Ohio, Inc. | Can coatings, methods for coating can and cans coated thereby |
BRPI0616274B1 (pt) | 2005-10-18 | 2017-12-05 | Valspar Sourcing, Inc. | Container understanding a metal food or drink container, method for preparing a container undertaking a metal food or drink container, and coating composition |
JP2007238698A (ja) | 2006-03-07 | 2007-09-20 | Toyo Ink Mfg Co Ltd | ポリマーエマルジョン含有水性塗料組成物 |
US7858162B2 (en) | 2006-04-06 | 2010-12-28 | Ppg Industries Ohio, Inc. | Food cans coated with a composition comprising an acrylic polymer |
MX2008014684A (es) | 2006-05-16 | 2008-11-28 | Du Pont | Composicion de recubrimiento altamente productiva para repintado automotriz. |
US7981515B2 (en) | 2006-05-30 | 2011-07-19 | Ppg Industries Ohio, Inc. | Bis epoxy polyesters and food cans coated with a composition comprising same |
WO2007138111A1 (en) | 2006-06-01 | 2007-12-06 | Cytec Surface Specialties, S.A. | Pressure sensitive adhesives |
EP2035475B1 (en) | 2006-07-05 | 2019-06-12 | Swimc Llc | Water-dispersible polyurethane polymer |
ATE528332T1 (de) | 2006-07-12 | 2011-10-15 | Mitsubishi Chem Corp | Verfahren zur herstellung von polyurethan und verwendung von danach hergestelltem polyurethan |
US8138262B2 (en) | 2006-11-21 | 2012-03-20 | Ppg Industries Ohio, Inc. | Waterborne, radiation-curable coating compositions and related methods |
JP2008297379A (ja) | 2007-05-30 | 2008-12-11 | Toyo Ink Mfg Co Ltd | 水性塗料及びその製造方法 |
US20090047531A1 (en) | 2007-08-17 | 2009-02-19 | Ppg Industries Ohio, Inc. | Packages having radiation-curable coatings |
JP5065190B2 (ja) | 2007-09-04 | 2012-10-31 | ローム アンド ハース カンパニー | 低腐食性硬化性組成物 |
US8227027B2 (en) | 2007-12-07 | 2012-07-24 | Presspart Gmbh & Co. Kg | Method for applying a polymer coating to an internal surface of a container |
US20090220795A1 (en) | 2008-02-29 | 2009-09-03 | Ppg Industries Ohio, Inc. | Composites comprising a multi-layer coating system |
GB0822674D0 (en) | 2008-12-12 | 2009-01-21 | Nuplex Resins Bv | A crosslinkable polymer binder |
US20100160561A1 (en) | 2008-12-24 | 2010-06-24 | Ppg Industries Ohio, Inc. | Copolymers of alpha-olefin type monomers and curable film-forming compositions containing them |
PL2382262T3 (pl) | 2009-01-20 | 2016-02-29 | Ppg Ind Ohio Inc | Przezroczyste, bezbarwne kompozycje pochłaniające promieniowanie podczerwone, zawierające nanocząstki niestechiometrycznego tlenku wolframu |
ES2655318T3 (es) | 2009-02-24 | 2018-02-19 | Akzo Nobel Coatings International B.V. | Emulsiones de látex y composiciones de revestimiento formadas a partir de emulsiones de látex |
EP2451880B1 (en) | 2009-07-07 | 2014-04-16 | Ak Steel Properties, Inc. | Polymer coated metallic substrate and method for making |
EP3208289A1 (en) | 2009-07-17 | 2017-08-23 | Valspar Sourcing, Inc. | Coating composition and articles coated therewith |
WO2011019082A1 (ja) | 2009-08-10 | 2011-02-17 | 独立行政法人科学技術振興機構 | オートファジーの測定方法 |
US9708504B2 (en) | 2010-04-01 | 2017-07-18 | Ppg Industries Ohio, Inc. | Branched polyester polymers and coatings comprising the same |
WO2011135536A2 (en) | 2010-04-29 | 2011-11-03 | Agricultural Research Organisation | Novel ruminant feed |
US9346959B2 (en) | 2010-12-08 | 2016-05-24 | Ppg Industries Ohio, Inc. | Non-aqueous dispersions comprising a nonlinear acrylic stabilizer |
EP2658933B1 (en) | 2010-12-29 | 2017-03-01 | Akzo Nobel Coatings International B.V. | Latex emulsions and coating compositions formed from latex emulsions |
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 |
US20130052380A1 (en) | 2011-08-29 | 2013-02-28 | Ppg Industries Ohio, Inc. | Coating compositions for food and beverage containers |
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