ES2599253T3 - Composiciones de revestimiento basadas en disolvente - Google Patents

Composiciones de revestimiento basadas en disolvente Download PDF

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Publication number
ES2599253T3
ES2599253T3 ES12805519.1T ES12805519T ES2599253T3 ES 2599253 T3 ES2599253 T3 ES 2599253T3 ES 12805519 T ES12805519 T ES 12805519T ES 2599253 T3 ES2599253 T3 ES 2599253T3
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coating compositions
hydroxyl functional
based coating
solvent based
reacting
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ES12805519.1T
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English (en)
Inventor
Cathy Li
Timothy I. Memmer
Daniel Bode
Stefan POSAKIWSKY
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Akzo Nobel Coatings International BV
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Akzo Nobel Coatings International BV
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F289/00Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds not provided for in groups C08F251/00 - C08F287/00
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D151/00Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D151/08Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D191/00Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Details Of Rigid Or Semi-Rigid Containers (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)

Abstract

Una composición de revestimiento curable preparada por un método que comprende: a) hacer reaccionar un aceite vegetal epoxidado con un material con funcionalidad hidroxilo en presencia de un catalizador ácido y un disolvente para formar un poliol de aceite con funcionalidad hidroxilo; b) mezclar el poliol de aceite con funcionalidad hidroxilo con un copolímero de poliolefina funcional para formar una mezcla; c) hacer reaccionar la mezcla con un componente de monómero etilénicamente insaturado en presencia de un iniciador para formar un copolímero de injerto; y d) mezclar el copolímero de injerto con un reticulante para formar la composición de revestimiento curable.

Description

imagen1
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imagen4
imagen5
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imagen10
Enamel Rater.
Se usó la resistencia a cloruro de cobre para medir la capacidad del sustrato revestido después de la retorta de agua para retener su integridad según experimenta un proceso de formación para producir un extremo para latas de bebida. En este ensayo, los extremos de lata fabricados se expusieron a una disolución de cloruro de cobre. El 5 cobre se depositará en cualquier grieta o fractura que pueda existir en el extremo. Se preparó una disolución de ensayo de sulfato de cobre con 2070 gramos de agua, 600 gramos de sulfato de cobre, 300 gramos de ácido clorhídrico y 30 gramos de Dowfax 2A1. El sulfato de cobre se disolvió en el agua destilada en un vaso de precipitados de 4000 ml, después se añadieron el ácido clorhídrico y Dowfax 2A1. El procedimiento de ensayo fue el siguiente: (1) llenar la bandeja hasta una profundidad de 12,7 mm (1/2 pulgadas) con la disolución de sulfato de
10 cobre; (2) hacer flotar los extremos con el lado interior hacia abajo sobre la disolución; (3) ajustar el temporizador durante 30 minutos; y (4) una vez transcurridos 30 minutos, retirar los extremos y sumergir en un recipiente de agua corriente. Se midió la corrosión visualmente usando una escala de 0-5. Una corrosión de 0 significa que no había manchas de cloruro de cobre en el extremo. Una corrosión de 5 significa que la película se había manchado completamente con cloruro de cobre.
15 Se usó un ensayo con ácido cítrico al 2% para simular una bebida ácida. Los extremos de la lata se sumergieron en la disolución de ácido cítrico al 2% durante 60 minutos a 121ºC (250ºF). Los resultados de ensayo se resumen en la Tabla 4. La corrosión en retorta y la adhesión se midieron de la misma manera que en los ejemplos anteriores.
Tabla 4
1
2 3 4 5 6
Retorta a 121ºC (250ºF) con vapor de agua (Enamel Rater)
17,9 6,1 73,37 10,23 0,8 3,67
Retorta de agua, sumergido 90 min a 121ºC (250ºF) (Enamel Rater)
6,3 6,1 43,10 5,2 2,6 4,23
Resistencia a la corrosión por exposición del metal a sulfato de cobre 30 minutos Pared del panel Remache Puntuación
1 < 1 < 1 0 < 1 < 1 0 1 < 1 0 < 1 0 0 0 0 0 0 0
ácido cítrico al 2% 60 min a 121ºC (250ºF)
Corrosión
1 1 1 0 0 0
Ampollas
No No No No No No
Adhesión
< 1 0 3 2 0 0
12

Claims (1)

  1. imagen1
    imagen2
ES12805519.1T 2011-12-21 2012-12-18 Composiciones de revestimiento basadas en disolvente Active ES2599253T3 (es)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201161578526P 2011-12-21 2011-12-21
US201161578526P 2011-12-21
EP12150245 2012-01-05
EP12150245 2012-01-05
PCT/EP2012/075875 WO2013092541A1 (en) 2011-12-21 2012-12-18 Solvent-based coating compositions

Publications (1)

Publication Number Publication Date
ES2599253T3 true ES2599253T3 (es) 2017-01-31

Family

ID=48667742

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Country Status (9)

Country Link
US (1) US9273226B2 (es)
EP (1) EP2794703B1 (es)
KR (1) KR102019726B1 (es)
CN (1) CN103998480B (es)
BR (1) BR112014014107B1 (es)
ES (1) ES2599253T3 (es)
MX (1) MX367933B (es)
RU (1) RU2605418C2 (es)
WO (1) WO2013092541A1 (es)

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US9593195B2 (en) 2013-03-15 2017-03-14 Akzo Nobel Coatings International B.V. Acrylic grafted polyether resins based on phenol stearic acid and coating compositions formed therefrom
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CN103739800B (zh) * 2014-01-14 2016-03-23 常州光辉化工有限公司 酚醛树脂漆用成膜物及其制备方法
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US9273226B2 (en) 2016-03-01
BR112014014107B1 (pt) 2020-12-08
BR112014014107A2 (pt) 2017-06-13
US20140364537A1 (en) 2014-12-11
EP2794703A1 (en) 2014-10-29
WO2013092541A1 (en) 2013-06-27
KR20140107300A (ko) 2014-09-04
MX2014007313A (es) 2014-07-28
CN103998480A (zh) 2014-08-20
EP2794703B1 (en) 2016-07-20
RU2014128543A (ru) 2016-02-20
KR102019726B1 (ko) 2019-09-09
CN103998480B (zh) 2016-10-19
RU2605418C2 (ru) 2016-12-20

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