WO2016148710A1 - Compositions de revêtement comprenant de l'urée et systèmes de revêtement multicouches comprenant celles-ci - Google Patents

Compositions de revêtement comprenant de l'urée et systèmes de revêtement multicouches comprenant celles-ci Download PDF

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Publication number
WO2016148710A1
WO2016148710A1 PCT/US2015/021213 US2015021213W WO2016148710A1 WO 2016148710 A1 WO2016148710 A1 WO 2016148710A1 US 2015021213 W US2015021213 W US 2015021213W WO 2016148710 A1 WO2016148710 A1 WO 2016148710A1
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Prior art keywords
composition
basecoat
urea compound
coating
layer
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PCT/US2015/021213
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English (en)
Inventor
Stephen Brian ISTIVAN
Justin BOHN
John HIXENBAUGH
Craig D. NIEDERST
David R. Fenn
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Ppg Industries Ohio, Inc.
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Priority to PCT/US2015/021213 priority Critical patent/WO2016148710A1/fr
Publication of WO2016148710A1 publication Critical patent/WO2016148710A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/60—Additives non-macromolecular
    • C09D7/63—Additives non-macromolecular organic
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2202/00—Metallic substrate
    • B05D2202/10—Metallic substrate based on Fe
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50—Multilayers
    • B05D7/52—Two layers
    • B05D7/53—Base coat plus clear coat type
    • B05D7/534—Base coat plus clear coat type the first layer being let to dry at least partially before applying the second layer
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/21—Urea; Derivatives thereof, e.g. biuret

Definitions

  • the present invention relates to liquid coating compositions that comprise a film-forming compound; an aqueous medium; and a urea compound. Methods of using the same and multilayer coating systems comprising the same are also within the scope of the present invention.
  • Coating compositions are used in a wide variety of applications, including, for example, the automotive, appliance and industrial industries. Coatings are often used to provide decorative qualities and/or corrosion protection to the substrates over which they are applied. Such coatings typically have a largely defect-free surface, and in the case of automotive decorative finishes, also a very smooth surface. The automotive industry has particularly strict requirements as to the appearance of the coatings that are used.
  • Automotive coatings are typically applied by spray applicators and therefore have a high shear viscosity of less than 150 cp (centipoise) to allow the coating to flow through the spray applicator. If the coating composition is too viscous, a solvent, such as water or organic solvent, may be added to the coating composition to achieve the desired high shear viscosity. Addition of the solvent, however, while reducing the high shear viscosity may also reduce the total solids in the coating composition. As a result multiple passes of the spray gun and/or a slower pass or flow of coating as the substrate is sprayed may be needed to achieve the desired film build. Compositions having a desired high shear viscosity and solid content are sought.
  • a solvent such as water or organic solvent
  • the present invention provides a liquid coating composition
  • a liquid coating composition comprising, (i) a film-forming compound; (ii) an aqueous medium; and (iii) a urea compound having the structure: wherein Rl and R2 are independently H or an alkyl group.
  • the present invention also provides a method of increasing total solid content while maintaining or reducing the high shear viscosity of a liquid coating composition
  • a method of increasing total solid content while maintaining or reducing the high shear viscosity of a liquid coating composition comprising: incorporating a urea compound into the coating composition, wherein the urea compound has the structure: wherein Rl and R2 are independently H or an alkyl group.
  • the present invention further provides a process for forming a multilayer coating on a substrate, the process comprising: forming a first basecoat layer over at least a portion of a substrate by depositing a first basecoat composition over at least a portion of the substrate, optionally, drying or curing the first basecoat layer; forming a second basecoat layer on at least a portion of the first basecoat layer by depositing a second basecoat composition, which can be the same or different from the first basecoat composition, directly onto at least a portion of the first basecoat layer, optionally, drying or curing the second basecoat layer; forming a clear coat layer on at least a portion of the second basecoat layer by depositing a clear coat composition directly onto at least a portion of the second basecoat layer; and curing any uncured coating layer, wherein the first basecoat layer and/or second basecoat layer comprise a urea compound having the
  • Rl and R2 are independently H or an alkyl group.
  • the present invention also provides a method of decreasing high shear viscosity of a liquid coating composition, wherein the total solid content of the composition increases or does not decrease by more than 4% comprising:
  • urea compound incorporating a urea compound into the coating composition in an amount of 0.1 to 30 weight percent based on the total weight of solid content in the composition, wherein the urea compound has the structure:
  • Rl and R2 are independently H or an alkyl group.
  • the present invention is generally directed to liquid coating compositions comprising: (i) a film- forming compound, (ii) an aqueous medium and (iii) a urea compound having the structur
  • Rl and R2 are independently H or an alkyl group.
  • any film-forming compound can be used according to the present invention.
  • a “film- forming compound”, “film-former”, or like terms refers to a compound that can form a self-supporting continuous film on at least a horizontal surface of a substrate.
  • the film-forming compound can be a polymer or resin that can crosslink with itself and/or a crosslinking agent upon cure.
  • Conventional film- forming compounds used in automotive OEM coating compositions, automotive refmish coating compositions, industrial coating compositions, architectural coating compositions, coil coating compositions, and aerospace coating compositions, for example, could all be used according to the present invention.
  • Suitable non-limiting examples of film forming compounds include those made from, acrylic polymers, alkyd polymers, polyester polymers, polyurethane polymers, polyether polymers, polyepoxide polymers, silicon-containing polymers, and mixtures thereof.
  • the film forming compound can comprise a self-crosslinking compound and/or can comprise a compound that cures upon reaction with a crosslinker or curing agent.
  • Suitable crosslinkers can be determined by one skilled in the art based upon the resin selected, and generally include aminoplasts, polyisocyanates, polyacids, carbodiimide, anhydrides and mixtures thereof.
  • a particular example of a film-former is a mixture of a polyurethane acrylic latex and a melamine crosslinker.
  • Film-forming compound collectively refers to a resin and crosslinker in those systems in which cure is achieved by use of a crosslinker.
  • the film forming compound may exclude urea in any form other than the urea described herein.
  • the coating compositions of the present invention can comprise 10 weight percent or greater film forming compound, with weight percent based on the total weight of the composition, such as 20 weight percent or greater, or 40 weight percent or greater.
  • the amount of film forming compound does not include the urea compound, even if the urea reacts with the film forming components.
  • the present coating compositions also comprise an aqueous medium.
  • An "aqueous medium” is a liquid medium that is 50 weight percent or greater of water, with weight percent based on non-solid content of the coating composition.
  • the aqueous medium may comprise less than 50 weight percent of other solvents, either organic or inorganic; these solvents may be substantially fully miscible with or soluble in water.
  • Suitable organic solvents include an ester, ketone, glycol ether, alcohol, hydrocarbon or mixtures thereof.
  • Suitable ester solvents include alkyl acetates such as ethyl acetate, n-butyl acetate, n-hexyl acetate, and mixtures thereof.
  • ketone solvents include methyl ethyl ketone, methyl isobutyl ketone, and mixtures thereof.
  • suitable hydrocarbon solvents include toluene, xylene, aromatic hydrocarbons such as those available from Exxon-Mobil Chemical Company under the SOLVESSO trade name, and aliphatic hydrocarbons such as hexane, heptanes, nonane, and those available from Exxon-Mobil Chemical Company under the ISOPAR and VARSOL trade names.
  • the present coating compositions can comprise 20 weight percent or greater aqueous medium, such as 30 weight percent or greater or 40 weight percent or greater, with weight percent based on the total weight of the composition.
  • the present coating compositions also comprise a urea compound represented by Structure 1 :
  • Rl and R2 are independently H or an alkyl group.
  • alkyl is meant any carbon containing compound or residue thereof, typically having one to twelve carbons, including alkyl and aralkyl, cyclic or acyclic, linear or branched monovalent hydrocarbon groups.
  • urea compound and like terms refers to the monomeric form of urea or alkyl urea and not the oligomeric form or polymeric form of urea such as polyurea or polyurethane. It will be appreciated that when both Rl and R2 are H, structure 1 represents urea, and when Rl and R2 are both methyl, structure 1 represents dimethylurea, each of which are particularly suitable for use in the present compositions.
  • the urea compound may be obtained in dry solid form and added to the liquid coating compositions.
  • the urea compound can be incorporated in a liquid carrier, such as water, prior to adding to the liquid coating compositions.
  • a solution can comprise a urea compound in the solution at an amount of 20 to 50 weight percent, or in an amount of 30 to 45 weight percent based on the total weight of the solution.
  • the urea compound can be present in coating compositions in an amount of 0.1 to 30 weight percent, based on the total solid weight of the composition, such as in an amount of 1 to 20, or in an amount of 2 to 12 weight percent.
  • the urea compound can also be present in an amount of 0.1 weight percent or greater, based on the total solid weight in the coating composition, such as in an amount of 2 weight percent or greater.
  • the urea compound can be present in an amount of 30 weight percent or less, based on the total solid weight in the coating composition, such as in an amount of 12 weight percent or less.
  • the total solid content of a coating composition can be measured by the methods outlined in the examples.
  • the urea compound can further be present in an amount of 1 weight percent or greater, based on the total weight of the water in the coating composition, such as in an amount of 5 weight percent or greater.
  • a weight percent described herein is based on the total weight of water, the calculation includes all of the water in the system, including water that comes in through the resin, any additives and the like, and does not include any other solvent.
  • the urea compound maybe selected and incorporated in an amount to increase the solids content while still achieving the desired coating high shear viscosity.
  • the coating compositions of the present invention may optionally include additional materials such as fillers, colorants, waxes, extenders, rheology modifiers, adhesion promoters, pigments, dispersants, plasticizers, anti-oxidants, hindered amine light stabilizers, UV light absorbers and stabilizers, surfactants, flow control agents, thixotropic agents, fillers, organic cosolvents, abrasion resistant particles, catalysts, grind vehicles, and other customary auxiliaries that are known to those skilled in the art.
  • “Colorant” is defined in U.S. Patent No. 8,614,286, at column 7, lines 5 to 23, which are incorporated by reference herein.
  • a urea compound according to the present invention increases the total weight percent of solids in a coating composition while at the same time decreasing the high shear viscosity. This is in contrast to many reactive diluents known in the art, which increase solids but typically also significantly increase high shear viscosity. This is also in contrast to organic solvents, which typically decrease high shear viscosity but do not increase the solids content. Similarly, water is often used to reduce the high shear viscosity of a coating composition but will also decrease the total solids content. Use of a urea compound instead of water, therefore, to decrease the high shear viscosity of a coating composition will serve to increase the total solids content of the composition.
  • the coating compositions of the present invention can have a higher total solids content than, and a high shear viscosity within plus or minus 20% of, a coating composition in which the urea compound has been replaced with an equal weight amount of water, such as a high shear viscosity within plus or minus 15% or plus or minus 10%>.
  • the present coatings can also have a higher total solids content than, and a high shear viscosity within plus 20% of, a coating composition in which the urea compound is replaced with an equal weight amount of water, such as within 15%, within 10% or within 8%.
  • the coating compositions of the present invention can have, for example, a high shear viscosity in the range of 40 cp to 150 cp, such as 80 cp to 120 cp.
  • high shear viscosity refers to viscosity as measured on a Brookfield model CAP- 2000+ viscometer (BYK-Gardner GmbH, Geretsried , DE) using a #4 Spindle at a speed of 300 RPM and at 25°C.
  • the present invention further provides a method for using a urea compound in a liquid coating composition to increase total solids content in the coating while decreasing the high shear viscosity of the coating.
  • the urea compound can be incorporated in an aqueous coating composition in an amount of 0.1 to 45 weight percent, or in an amount of 1 to 30 weight percent, or in an amount of 3 to 18 weight percent based on the total water content of the aqueous coating composition.
  • the total solid content of the composition will increase, while the high shear viscosity of the composition will be within plus or minus 20%> of the high shear viscosity if water were used in an equal weight amount to achieve a reduction in the coating composition high shear viscosity.
  • the present invention also provides a method of decreasing high shear viscosity of a liquid coating composition, wherein the total solid content of the composition increases or does not decrease by more than 4%.
  • the urea compound content can be incorporated into the coating composition in an amount of 0.1 to 30 weight percent, such as in an amount of 1 to 20 weight percent, or in an amount of 2 to 12 weight percent based on the total weight of solid content in the composition. According to the present invention, for example, if a urea compound is incorporated into a coating composition in a sufficient amount to decrease the high shear viscosity, while the total solid content of the coating composition can increase or not decrease by more than 4%.
  • a urea compound can be incorporated into the coating composition in an amount to decrease the high shear viscosity while the total solid content of the composition can increase or not decrease to less than 96% of the original total solid content. For example, if a coating composition has an initial total solid content of 50 weight percent, the addition of a urea compound can increase the total solid content to more than 50 weight percent or not decrease the total solid content to less than 48 weight percent.
  • the coating compositions of the present invention can be applied to any substrates known in the art. These substrates can be, for example, metallic or non- metallic.
  • Metallic substrates include tin, steel, tin-plated steel, chromium passivated steel, galvanized steel, aluminum, aluminum foil, coiled steel or other coiled metal.
  • Non-metallic substrates including polymeric, plastic, polyester, polyolefm, polyamide, cellulosic, polystyrene, polyacrylic, poly(ethylene naphthalate), polypropylene, polyethylene, nylon, EVOH, polylactic acid, other "green” polymeric substrates, poly(ethyleneterephthalate) ("PET”), polycarbonate, polycarbonate acrylobutadiene styrene (“PC/ABS”), polyamide, wood, veneer, wood composite, particle board, medium density fiberboard, cement, stone and the like.
  • the substrate can be one that has been already treated in some manner, such as to impart visual and/or color effect, a protective pretreatment or other coating layer, and the like.
  • the coating compositions of the present invention can be applied by any means standard in the art, such as electrocoating, spraying, electrostatic spraying, dipping, rolling, brushing, and the like.
  • the high shear viscosity of the coating compositions of the present invention can be adjusted to a desired high shear viscosity without negatively impacting the total solid content of the coating compositions. Accordingly, spray application is a particularly suitable method of application.
  • the coating compositions of the present invention can, for example, be used in the formation of multilayer coating systems, which may include two or more layers at least one of which may be deposited from any of the coating compositions described above.
  • multilayer coating systems may include a basecoat layer and a clear coat layer.
  • the multilayer coating systems can further include a second basecoat layer and an optional electrodeposition coat layer.
  • the coating compositions of the present invention are particularly suitable for use in a compact coating process.
  • a “compact coating process” or “compact process” is one in which at least one curing step has been eliminated from a standard automotive coating process; stated another way, one or more curing steps are combined in a compact coating process in that one or more coating layers may be deposited on a previous coating layer, which may optionally be dried but not cured, in a "wet-on-wet” application and the layers cured simultaneously.
  • a compact process will eliminate the use of, and need to cure, a primer-surfacer layer; in the compact process a standard primer-surfacer layer can be replaced with a first basecoat layer.
  • Some compact coating processes apply two basecoat layers, also known as a first basecoat layer (Bl) and a second basecoat layer (B2), to a substrate.
  • the liquid coating compositions disclosed herein can be used as a basecoat composition that forms either or both the first basecoat layer and second basecoat layer.
  • the optional electrodeposition coating compositions of the multilayer coating systems may include conventional anionic or cationic electrodepositable coating compositions, such as epoxy or polyurethane -based coatings. Suitable
  • the cured electrodeposited layer if used, can have a dry-film thickness has high as 100 micrometers, such as 15 to 50 micrometers.
  • the basecoats when they are used in multilayer coating systems, they can be deposited from the present coating compositions.
  • Other suitable basecoat compositions that may be used in multilayer coating systems of the present invention are discussed in U.S. Pat. Nos. 8,152,982 and 8,846,156. If two or more basecoats are used, the basecoats can be the same or different. "Different" can include two different coating compositions according to the present invention. After application to at least a portion of the substrate, the first basecoat composition can be dried at ambient or elevated temperatures such as by forced air, or thermally cured.
  • “Dried”, “drying” and like terms when used in reference to an application of the coating layers, refers to removal of at least some water and/or solvent from the coating composition at temperatures lower than those needed to cure the coating and includes, for example, processes such as flashing or dehydrating.
  • drying can include a "flash", which is generally performed by exposing a coated substrate to ambient or slightly elevated temperatures (typically 40°C or lower) for a brief period of time (typically 30 seconds to 20 minutes) to remove some solvent(s) but not as much as in a dehydrating process, in which a coated substrate is exposed to temperature (typically in the range of 40°C to 121°C) for a period of time sufficient to remove solvents but insufficient to cure the coated substrate, such as 1 to 10 minutes.
  • ambient it is meant that at least a portion of the solvents, e.g. including water or organic solvents, in the coating compositions can be removed without the aid of heat or other energy, for example, without baking in an oven, use of forced air, or the like.
  • a second basecoat layer can be deposited on at least a portion of substrate coated with the first basecoat and the coated substrate subjected again to a drying step as described above. If the first basecoat was only dried, and not cured, then the two basecoat layers can be cured simultaneously at this time. It will be appreciated that one curing step can therefore be eliminated by the wet-on- wet application of the second basecoat over the uncured first basecoat and simultaneous curing of the two basecoats together.
  • the dry-film thickness of the first and second basecoat layers can be as high as 100 micrometers, but usually ranges from 1 to 50, such as from 5 to 30, or from 10 to 25 micrometers.
  • the multilayer coating systems can further comprise a clear coat layer.
  • a clear coat layer will be understood as a coating that is substantially transparent. A clear coat can therefore have some degree of color, provided it does not make the clear coat opaque or otherwise affect, to any significant degree, the ability to see the underlying substrate.
  • the clear coat layer can be formed from either one component ("IK"), or multi-component compositions such as two component (“2K”) or more.
  • IK one component
  • 2K multi-component compositions
  • a IK composition will be understood as referring to a composition wherein all the coating components are maintained in the same container after manufacture, during storage, etc., while a 2K or multi-component composition will have two or more components that are stored separately and mixed just prior to application. Clear coat compositions are known in the art for automotive applications.
  • the multilayer coating systems of the present invention can include, for example, a clear coat layer deposited on at least a portion of the substrate coated with the one or more basecoat layers as described above.
  • the clear coat layer can be applied to a basecoat layer and cured using any conventional means. It will be appreciated that the clear coat can be applied to a dried but uncured basecoat and the layers cured simultaneously, or the basecoat(s) can be cured prior to application of the clear coat. Once applied and cured, the clear coat layer can have a dry- film thickness of 100 micrometers such as from 30 to 50 micrometers.
  • the multilayer coating systems of the present invention which can comprise two layers including one or two basecoat layers and/or a clear coat layer, wherein at least one of the basecoat layers is formed from a coating composition of the present invention, can demonstrate equivalent or improved appearance, as measured by shortwave or longwave scanning with a Byk Wave-scan Dual machine, as compared to similar multilayer coating systems that do not use a urea compound.
  • a multilayer coating system can exhibit an improvement in appearance of at least 0.5 units, such as 1.0 or more units, based on shortwave scanning, as compared to similar cured multilayer coating systems having the same components but lacking the urea compound.
  • the shortwave and longwave appearance number are determined in accordance with a Byk Wave-scan Dual (BYK-Gardner GmbH, Geretsried, DE at standard temperature (25°C).
  • the present invention is also directed to a method for forming a multilayer coating system on a substrate, the method comprising: forming a first basecoat layer over at least a portion of a substrate by depositing a first basecoat composition over at least a portion of the substrate; optionally, drying or curing the first basecoat layer; optionally forming a second basecoat layer over at least a portion of the first basecoat layer by depositing a second basecoat composition directly onto at least a portion of the first basecoat layer; optionally, drying or curing the second basecoat layer;
  • first basecoat layer and/or second basecoat layer comprise a urea compound having Structure 1.
  • the second basecoat composition can be the same or different from the first basecoat composition. It will be appreciated that the first and second basecoat, if used, can be cured individually, can be cured simultaneously, in both cases prior to forming the subsequent coating layer, or can be cured simultaneously with the clear coat.
  • the process can further include the step of forming an
  • electrodeposition coating layer by electrodepositing an electrodepositable coating composition on at least a portion of the substrate prior to the step of forming the first basecoat layer.
  • the electrodeposition coating layer can be dried or cured prior to forming the first basecoat layer.
  • polymer is meant to refer to prepolymers, oligomers and both homopolymers and copolymers; the prefix “poly” refers to two or more.
  • any endpoints of those ranges and/or numbers within those ranges can be combined with the scope of the present invention.
  • “Including”, “such as”, “for example” and like terms means “including/such as/for example but not limited to”.
  • a liquid coating composition comprising:
  • Rl and R2 are independently H or an alkyl group.
  • a method for coating a substrate comprising:
  • a method of increasing total solid content while maintaining or reducing the high shear viscosity of a liquid coating composition comprising:
  • urea compound incorporating a urea compound into the coating composition, wherein the urea compound has the structure:
  • Rl and R2 are independently H or an alkyl group.
  • a process for forming a multilayer coating system on a substrate comprising:
  • first basecoat layer forming a first basecoat layer over at least a portion of a substrate by depositing a first basecoat composition over at least a portion of the substrate;
  • forming a second basecoat layer on at least a portion of the first basecoat layer by depositing a second basecoat composition, which is the same or different from the first basecoat composition, directly onto at least a portion of the first basecoat layer; optionally, drying or curing the second basecoat layer; forming a clear coat layer on at least a portion of the second basecoat layer by depositing a clear coat composition directly onto at least a portion of the second basecoat layer; and
  • first basecoat layer and/or second basecoat layer comprise a urea compound having the structure:
  • Rl and R2 are independently H or an alkyl group.
  • composition wherein the total solid content of the composition increases or does not decrease by more than 4% comprising:
  • urea compound incorporating a urea compound into the coating composition in an amount of 0.1 to 30 weight percent based on the total weight of solid content in the composition, wherein the urea compound has the structure:
  • Rl and R2 are independently H or an alkyl group.
  • a white basecoat composition was prepared according to Example 1 described in US 8,846,156 B2, which is incorporated in pertinent part herein, and had 22 weight percent resin solids, 30 weight percent pigment solids, 54 weight percent total solids, 8 weight percent organic solvent and 38 weight percent water, with all weight percents based on the total weight of the composition. This basecoat was used as a control.
  • Example 2 urea or water was incorporated in the control basecoat composition (Example 1) in amounts shown below in Table 1.
  • the urea compound, added as a solid, or the water was added to the control basecoat composition and stirred for at least ninety (90) minutes.
  • the total water content was based on the water content in the entire basecoat composition including, for example, the water content of the resin but did not include an other solvents.
  • Basecoat % Urea Level is defined as the ratio of grams of urea added as a percentage of the total grams of non- volatile materials (i.e. solid content) in the basecoat multiplied by one hundred.
  • 4Basecoat % Additional Water Level is defined as the ratio of grams of additional water added as a percentage of the total grams of non-volatile materials (i.e. solid content) in the basecoat multiplied by one hundred.
  • Examples 2, 4, 6 and 8 demonstrate that urea can be used to decrease the high shear viscosity of a basecoat composition while increasing the solids content of a basecoat.
  • Examples 3, 5, 7 and 9 in contrast, while water served to reduce the high shear viscosity of the basecoat, the total solids content of the composition also decreased.
  • the high shear viscosity of the present compositions (Examples 2, 4, 6 and 8) was within approximately 12% of the compositions comprising water instead (Examples 3, 5, 7 and 9).
  • a high shear viscosity that was still suitable for spray application was achieved, as was an increase in the total solids.
  • a gray basecoat composition was prepared according to Example 8 described in US 8,846,156 B2, which is incorporated in pertinent part herein, and had 29 weight percent resin solids, 15 weight percent pigment solids, 46 weight percent total solids, 12 weight percent organic solvent and 42 weight percent water, with all weight percents based on the total weight of the composition. This basecoat was used as a control.
  • urea or additional water was incorporated in the control basecoat composition (Example 10) in amounts shown below in Table 3 directly to the control basecoat composition (Example 10) and stirred for at least ninety (90) minutes.
  • the urea compound was added as a solution made by combining the amount of urea and water indicated and mixing as a solution for ninety (90) minutes.
  • the total water content was based on the water content in the entire basecoat composition including, for example, the water content of the resin but did not include an other solvents.
  • Basecoat % Urea Level is defined as the ratio of grams of urea added as a percentage of the total grams of nonvolatile materials (i.e. solid content) in the basecoat multiplied by one hundred.
  • 'Basecoat % Additional Water Level is defined as the ratio of grams of additional water added as a percentage of the total grams of non-volatile materials (i.e. solid content) in the basecoat multiplied by one hundred.
  • the total water content was based on the water content in the entire basecoat composition including, for example, the water content of the resin but did not include any other solvents.
  • Basel refers to the gray basecoat of Example 10 and Base2 refers to the white basecoat of Example 1.
  • Either a urea solution or additional water was added to Base2 as indicated in the above table.
  • the urea solution was prepared by mixing the indicated amount of water and urea for ninety (90) minutes.
  • Each Basel and Base2 was spray applied using a Compuspray Automatic Test Panel Machine (Spraymaiton, Inc.) equipped with a 95 AR spraygun (Binks, Inc.) at 60 PSI using a 10 inch fan patter, 2 inch index distance, 6 inch initial index position up from bottom, and 10 strokes per coat. Both Basel and Base 2 were spray applied in an environment controlled to 70-75° F. (21-24° C.) and 50-60% relative humidity onto 4 inch by 12 inch (10 cm by 30 cm) steel panels that were coated with cured 6060CZ electrocoat commercially available from PPG Industries, Inc. Basel was applied in one coat and then flashed at ambient temperature for 5 minutes.
  • Base2 was then applied in two coats, without a flash between coats, and then flashed at ambient temperature for 5 minutes and then dehydrated for 5 minutes at 185° F. (85° C).
  • the film thicknesses of Basel and Base2 were approximately 0.6 mils (15 microns) and 0.8 mils (20 microns), respectively. Dry film thickness measurements were made using a Feritscope FMP30 (Fischer, Windsor T).
  • TKAPOIOOO a 2K clear coat composition commercially available from PPG Industries, Inc.
  • the clear coated panels were allowed to flash for 10 minutes at ambient conditions and baked for 30 minutes at 285° F. (140° C).
  • the clear coat had a dry film thickness of approximately 1.8 mils (45 microns).
  • Appearance was measured using a Byk Wave-scan Dual instrument (BYK- Gardner GmbH, Geretsried , DE). Longwave, shortwave, and DOI (GM) values were taken and the average of three measurements reported in Table 6 below. All measurements were taken at standard temperatures (25°C). Lower BYK Wave-scan values of longwave and shortwave are more desirable; higher values of DOI(GM) and total solids are more desirable.
  • 13 % B2 Urea Level is defined as the ratio of grams of urea added as a percentage of the total grams of non-volatile materials (i.e. solid content) in the white B2 basecoat multiplied by one hundred.
  • 14 % B2 Additional Water Level is defined as the ratio of grams of water added as a percentage of the total grams of non- volatile materials (i.e. solid content) in the white B2 basecoat multiplied by one hundred.
  • Example 19 The solids and appearance data for Examples 1, 19 and 20 demonstrate the benefit of using a urea compound in at least one basecoat composition on the appearance of cured multilayer coating system. While lower longwave and shortwave numbers and higher DOI numbers were achieved with either additional water (Example 19) or urea (Example 20) as compared to the control, overall better appearance and higher solids can be achieved when using a urea solution as compared to an equal weight amount of water.

Abstract

L'invention concerne une composition de revêtement liquide, qui comprend (i) un composé filmogène ; (ii) un milieu aqueux ; et (iii) un composé urée. L'invention concerne également des procédés d'utilisation d'une telle composition de revêtement, et des systèmes de revêtement multicouches comprenant une telle composition de revêtement.
PCT/US2015/021213 2015-03-18 2015-03-18 Compositions de revêtement comprenant de l'urée et systèmes de revêtement multicouches comprenant celles-ci WO2016148710A1 (fr)

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Publication number Priority date Publication date Assignee Title
US4108001A (en) * 1976-09-23 1978-08-22 Westinghouse Electric Corp. Urea composition for forming thermoparticulating coating
GB2137218A (en) * 1980-11-05 1984-10-03 Tikkurilan Vaeritehtaat Oy Coating composition
EP0211359A1 (fr) * 1985-07-26 1987-02-25 Union Carbide Corporation Compositions de revêtement à forte teneur en solides
EP0212380A2 (fr) * 1985-08-01 1987-03-04 Union Carbide Corporation Compositions aqueuses de matériaux pour revêtement contenant une haute teneur en substance solide
WO1995026378A1 (fr) * 1994-03-29 1995-10-05 Henkel Corporation Composition et procede permettant de rendre la peinture moins collante
WO1996014144A1 (fr) * 1994-11-02 1996-05-17 Union Carbide Chemicals & Plastics Technology Corporation Procede et appareil servant a doser et melanger des fluides compressibles et non compressibles
WO1996035740A1 (fr) * 1995-05-08 1996-11-14 Henkel Corporation Dispersion de resine aminique avec reduction de la concentration d'aldehyde, procede correspondant et procede selon l'invention permettant de supprimer la tendance au collant de la peinture
WO1998058989A1 (fr) * 1997-06-20 1998-12-30 Coloplast A/S Revetement hydrophile et procede de preparation dudit revetement
WO2006063304A1 (fr) * 2004-12-10 2006-06-15 Basf Corporation Composition de revetement
EP1801161A1 (fr) * 2004-10-12 2007-06-27 Toray Industries, Inc. Formulation de resine impermeable aux gaz et pellicule impermeable aux gaz
JP2008037917A (ja) * 2006-08-02 2008-02-21 Sakura Color Prod Corp 水性絵具組成物
DE102007018652A1 (de) * 2007-04-20 2008-10-23 Bayer Materialscience Ag Nanoharnstoffe zur Reduzierung des VOC-Wertes wässriger Dispersionen
US20090011274A1 (en) * 2006-03-08 2009-01-08 Hiroyuki Ogata Coated Steel Sheet, Finished Product, Panel for Use in Thin Television Sets, and Method for Manufacturing Coated Steel Sheet
JP2009067910A (ja) * 2007-09-14 2009-04-02 Asahi Kasei Chemicals Corp 水性塗料用添加剤及び、水性塗料組成物
WO2011091806A1 (fr) * 2010-01-27 2011-08-04 El Sayed Kamel Morsy Elbaialy Composition ignifuge et anti-termites et articles revêtus de celle-ci
US20110281115A1 (en) * 2010-05-13 2011-11-17 Kania Charles M Curable film-forming compositions containing ortho-hydroxyl aromatic functional acrylic polymers

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4108001A (en) * 1976-09-23 1978-08-22 Westinghouse Electric Corp. Urea composition for forming thermoparticulating coating
GB2137218A (en) * 1980-11-05 1984-10-03 Tikkurilan Vaeritehtaat Oy Coating composition
EP0211359A1 (fr) * 1985-07-26 1987-02-25 Union Carbide Corporation Compositions de revêtement à forte teneur en solides
EP0212380A2 (fr) * 1985-08-01 1987-03-04 Union Carbide Corporation Compositions aqueuses de matériaux pour revêtement contenant une haute teneur en substance solide
WO1995026378A1 (fr) * 1994-03-29 1995-10-05 Henkel Corporation Composition et procede permettant de rendre la peinture moins collante
WO1996014144A1 (fr) * 1994-11-02 1996-05-17 Union Carbide Chemicals & Plastics Technology Corporation Procede et appareil servant a doser et melanger des fluides compressibles et non compressibles
WO1996035740A1 (fr) * 1995-05-08 1996-11-14 Henkel Corporation Dispersion de resine aminique avec reduction de la concentration d'aldehyde, procede correspondant et procede selon l'invention permettant de supprimer la tendance au collant de la peinture
WO1998058989A1 (fr) * 1997-06-20 1998-12-30 Coloplast A/S Revetement hydrophile et procede de preparation dudit revetement
EP1801161A1 (fr) * 2004-10-12 2007-06-27 Toray Industries, Inc. Formulation de resine impermeable aux gaz et pellicule impermeable aux gaz
WO2006063304A1 (fr) * 2004-12-10 2006-06-15 Basf Corporation Composition de revetement
US20090011274A1 (en) * 2006-03-08 2009-01-08 Hiroyuki Ogata Coated Steel Sheet, Finished Product, Panel for Use in Thin Television Sets, and Method for Manufacturing Coated Steel Sheet
JP2008037917A (ja) * 2006-08-02 2008-02-21 Sakura Color Prod Corp 水性絵具組成物
DE102007018652A1 (de) * 2007-04-20 2008-10-23 Bayer Materialscience Ag Nanoharnstoffe zur Reduzierung des VOC-Wertes wässriger Dispersionen
JP2009067910A (ja) * 2007-09-14 2009-04-02 Asahi Kasei Chemicals Corp 水性塗料用添加剤及び、水性塗料組成物
WO2011091806A1 (fr) * 2010-01-27 2011-08-04 El Sayed Kamel Morsy Elbaialy Composition ignifuge et anti-termites et articles revêtus de celle-ci
US20110281115A1 (en) * 2010-05-13 2011-11-17 Kania Charles M Curable film-forming compositions containing ortho-hydroxyl aromatic functional acrylic polymers

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