US20040191484A1 - Strippable laminate finish - Google Patents
Strippable laminate finish Download PDFInfo
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- US20040191484A1 US20040191484A1 US10/821,560 US82156004A US2004191484A1 US 20040191484 A1 US20040191484 A1 US 20040191484A1 US 82156004 A US82156004 A US 82156004A US 2004191484 A1 US2004191484 A1 US 2004191484A1
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- topcoat
- intermediate coating
- coated substrate
- coating
- strip agent
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group; Thio analogues thereof
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
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- 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
- B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
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- 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
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0017—Multi-phase liquid compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3945—Organic per-compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—Solvents
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
- C11D7/5022—Organic solvents containing oxygen
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- 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
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/32—Processes for applying liquids or other fluent materials using means for protecting parts of a surface not to be coated, e.g. using stencils, resists
- B05D1/322—Removable films used as masks
- B05D1/325—Masking layer made of peelable film
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- 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
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/06—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
- B05D3/061—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation using U.V.
- B05D3/065—After-treatment
- B05D3/067—Curing or cross-linking the coating
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/2034—Monohydric alcohols aromatic
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24479—Structurally defined web or sheet [e.g., overall dimension, etc.] including variation in thickness
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
- Y10T428/265—1 mil or less
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2139—Coating or impregnation specified as porous or permeable to a specific substance [e.g., water vapor, air, etc.]
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2213—Coating or impregnation is specified as weather proof, water vapor resistant, or moisture resistant
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/259—Coating or impregnation provides protection from radiation [e.g., U.V., visible light, I.R., micscheme-change-itemave, high energy particle, etc.] or heat retention thru radiation absorption
Definitions
- This invention relates to a strippable laminate finish, a strippable laminate finish kit, and methods for applying and for removing a finish.
- UV light curable coating compositions typically provide a desirable combination of properties including rapid cure, high gloss and good durability. Due to these properties and their generally good scratch and detergent resistance, UV light curable coating compositions have been used as floor finishes. Eventually even a UV light cured floor finish will show the effects of wear, and will require removal and renewal. UV cured floor finishes generally are not regarded as being removable using conventional chemical floor stripping agents. Instead, more aggressive removal techniques such as floor sanding or aggressive burnishing may be employed, thereby leading to removal of a portion of the underlying floor surface. This has discouraged the use of UV cured floor finishes.
- the present invention provides, in one aspect, a coated substrate comprising a strippable intermediate coating atop the substrate, and a strip agent-permeable coating atop the intermediate coating, wherein the strip agent-permeable coating is less strippable and more wear-resistant than the intermediate coating.
- the substrate comprises a floor
- the strip agent-permeable coating comprises a UV curable floor finish
- the intermediate coating comprises a metal-crosslinked acrylic
- the strip agent comprises a chemical strip agent containing a phenyl alcohol.
- the strip agent-permeable coating (which in the interest of brevity could be referred to as the topcoat, even though it may itself be overcoated with one or more other layers) protects the underlying intermediate coating and substrate from abrasion, dirt, and other environmental effects.
- a strip agent e.g., chemical strip agent
- the intermediate coating breaks down due to the action of the strip agent, thereby enabling removal of the intermediate coating and topcoat without the need for the use of aggressive removal techniques such as floor sanding or aggressive burnishing.
- the invention provides a strippable laminate finish kit, comprising one or more containers of a strippable intermediate coating and a strip agent-permeable topcoat, wherein the topcoat is less strippable and more wear resistant than the intermediate coating.
- the strippable laminate finish kit optionally includes a strip agent.
- the invention provides a strip agent concentrate containing a polar solvent that is denser than water, and a sufficiently low level of cosolvent or surfactant so that upon mixing with water a pseudo-stable aqueous dispersion forms which will phase-separate following application to a surface.
- the invention provides a method for applying a finish to a substrate, comprising the steps of applying to the substrate a strippable intermediate coating, allowing the intermediate coating to dry or harden, and applying a strip agent-permeable topcoat to the intermediate coating, wherein the topcoat is less strippable and more wear resistant than the intermediate coating.
- the invention provides a method for removing a multilayer laminate finish having a topcoat and an intermediate later atop a substrate, comprising the steps of applying to the topcoat a strip agent (e.g., a chemical strip agent), allowing the strip agent to permeate through the topcoat to attack the intermediate layer, and removing the intermediate layer and topcoat by mopping, vacuuming, mild abrasion or other measures that do not remove substantial portions of the underlying substrate.
- a strip agent e.g., a chemical strip agent
- FIG. 1 shows a view in cross-section of a floor coated with a laminate finish of the invention.
- FIG. 2 shows a view in cross-section of a wall coated with a laminate finish of the invention.
- FIG. 3 shows a view in cross-section of the application of a chemical strip agent to a laminate finish in the invention.
- FIG. 4 shows a view in cross-section illustrating removal of a laminate finish of the invention.
- a coating is regarded as being “strippable” if when subjected to the action of a suitable strip agent, the coating can readily be removed from the substrate using simple, non-abrasive measures such as a mop and detergent solution, or mildly abrasive but substrate-non-damaging measures such as a nonwoven floor scrub pad.
- Strippability preferably is evaluated using the Second Strippability Evaluation Method (7 point scale) set out below in the Example section, using Test Strip Agent K and a 10 minute strip agent standing time.
- a topcoat is regarded as being “strip agent-permeable” if when coated atop the desired strippable coating and subjected to the action of a suitable strip agent, the strip agent permeates or otherwise penetrates the topcoat sufficiently so that the both the topcoat and strippable coating can be removed from the substrate.
- Strip agent permeability can be enhanced by a mechanically roughening the topcoat (using, for example, a nonwoven floor scrub pad, brush or other mild abrasive measure) just prior to stripping.
- a topcoat will be regarded as being strip agent-permeable even if such mechanical roughening is required, so long as the required mechanical roughening does not damage the underlying substrate.
- a topcoat is regarded as being more wear resistant than an underlying strippable intermediate coating when the topcoat exhibits lower weight loss than the underlying intermediate coating using a Taber Abrasion test conducted according to ASTM D4060-95.
- topcoat 14 is a UV-curable floor finish whose wear resistance and durability protect underlying intermediate coating 12 and floor 10 from dirt, scuffing and other environmental factors.
- Intermediate coating 12 is a metal-catalyzed acrylic floor finish having lower wear resistance than topcoat 14 . If used alone on floor 10 , intermediate coating 12 could readily be stripped from floor 10 using a conventional chemical floor stripping agent. If used alone on floor 10 , topcoat 12 would not be strippable (or might only be stripped with difficulty) from floor 10 using such a stripping agent.
- FIG. 2 shows a wall 20 overcoated with wallpaper 22 and protective laminate finish 24 containing intermediate coating 26 and topcoat 28 .
- Topcoat 28 is an acrylic latex paint whose wear resistance and durability protect underlying intermediate coating 26 .
- wallpaper 22 and wall 20 from scuffing, abrasion and other wear or damage.
- Intermediate coating 26 is a metal-catalyzed acrylic coating having lower wear resistance than topcoat 28 . If used alone on wall 20 , intermediate coating 22 could readily be stripped from wall 20 using a thickened version of a conventional chemical floor stripping agent. If used alone on wall 20 , topcoat 24 would not be strippable (or might only be stripped with difficulty) from wall 20 using such a stripping agent.
- FIG. 3 shows the application of chemical stripping agent 30 to the laminate finish 11 of FIG. 1, and FIG. 4 shows the subsequent removal of the softened laminate finish 11 .
- agent 30 permeates and penetrates topcoat 14 but does not significantly soften or otherwise attack topcoat 14 .
- agent 30 causes intermediate coating 12 to soften and break apart.
- Intermediate coating 12 loosens its bond with floor 10 and begins a gradual disintegration process (illustrated in FIG. 4) that eventually causes intermediate coating 12 and topcoat 14 to break up into small particles such as particles 42 , 43 and 44 .
- Vacuum 48 facilitates removal of the residue of the laminate finish 11 from floor 12 .
- flooring materials that can be coated include resilient materials such as vinyl flooring, vinyl composite flooring, and synthetic sports floors; and non-resilient materials such as concrete, marble and wood.
- Other substrates that can be coated include walls, ceilings, labels, emblems, indoor and outdoor signs, and vehicles such as automobiles.
- a variety of intermediate coating materials can be employed. Suitable intermediate coating materials should be strippable using a strip agent that is capable of permeating the topcoat. Thus, the choice of intermediate coating material will be determined in part by the chosen topcoat and stripping agent. Waterborne intermediate coatings materials are preferred for ease of application. Water-soluble acid-containing polymers crosslinked using transition metals (e.g., metal crosslinked acrylics) are a particularly preferred class of intermediate coating materials. These can be stripped using a variety of strip agents (described in more detail below) that dissolve the intermediate coating or attack the crosslinking site.
- strip agents described in more detail below
- Preferred intermediate coatings will have a rating of 6 or more, more preferably a rating of 7, when coated alone on a vinyl composite tile substrate and evaluated using second Strippability Evaluation Method (7 point scale), using Test Strip Agent K and a 10 minute strip agent standing time.
- Suitable commercially available metal crosslinked acrylic polymers include Gemstar LaserTM and Taj MahalTM acrylic finishes from Ecolab Inc.; High NoonTM acrylic finish from Butchers; CitationTM acrylic finish from Buckeye International, Inc., SignatureTM, VectraTM, and CompleteTM acrylic finishes from SC Johnson Professional Products; Upper LimitsTM acrylic finish from Spartan Chemical Co.; and materials such as those described in U.S. Pat. Nos. 4,517,330 and 5,319,018 and the patents cited therein.
- Strippable floor coatings designated as “sealers” e.g., Over and UnderTM floor sealer, available from S. C. Johnson Professional Products
- Strippable coatings based on polyvinylacetates could also be used.
- two or more layers of different intermediate coatings can be employed in laminate finishes of the invention, in order to optimize properties such as adhesion to the substrate or to the topcoat, wear resistance, strippability, etc.
- topcoat materials can be used in the invention. Suitable topcoat materials should be less strippable than the intermediate coating, and should be permeable by a chemical strip agent that is capable of stripping the intermediate coating material. Thus, the choice of topcoat material will be determined in part by the chosen intermediate coating material and stripping agent. Preferred topcoat materials will have a rating of 5 or less, and more preferably a rating of 3 or less, if coated alone on a vinyl composite tile substrate and evaluated using the second Strippability Evaluation Method (7 point scale), Test Strip Agent K and a 10 minute strip agent standing time. When the intermediate coating and topcoat are each coated alone and compared using such an evaluation method, they preferably will have at least a 1 point differential, more preferably at least a 2 point differential, and most preferably at least a 4 point differential in observed strippability rating values.
- topcoat materials e.g. two-part thermally curable or one-part photocurable materials
- topcoat materials that are waterborne or otherwise substantially solvent free (e.g., 100 percent solids low viscosity formulations) are preferred for environmental reasons.
- the topcoat is not metal crosslinked.
- Suitable topcoat materials include urethanes, acrylics, epoxies, melamines and blends or copolymers thereof.
- Waterborne UV curable acrylates and urethanes are particularly preferred topcoat materials. These tend to be less strippable and more wear resistant than the metal crosslinked acrylic intermediate coatings mentioned above, and are permeable by strip agents that can be used to remove such intermediate coating materials.
- Suitable commercially or experimentally available topcoat materials include UV curable acrylates, urethanes and urethane acrylates (including aliphatic polyester urethane acrylates) such as the materials designated as 935-63 through 935-67; 935-75B; 935-76 and 935-80 through 935-82 series of UV curable coatings from UV Coatings Limited; RoShieldTM 3120 UV curable acrylate coating from Rohm & Haas; and NeoRadTM NR-3709 UV curable aliphatic urethane coating from Zeneca Resins, and materials such as those described in U.S. Pat. Nos. 5,453,451 and 5,773,487.
- a variety of other coating resins that can be cured using suitable crosslinking agents, thermal initiators or photoinitiators can be employed, including Courtmaster IITM waterborne acrylic urethane available from Ecolab, Inc.; LaromerTM PE 55W polyester acrylate, LR 8895 polyester acrylate, LR 8949 aliphatic urethane and LR 8983 aromatic urethane waterborne acrylic ester resins, all available from BASF Corp.; ViaktinTM VTE 6155 aliphatic urethane acrylate. VTE 6165 aromatic urethane acrylate and VTE 6169 aliphatic polyester urethane radiation curing resins, all available from Vianova Resins GmbH & Co.
- topcoats can be employed in laminate finishes of the invention, in order to optimize properties such as adhesion to the intermediate coating, laminate surface appearance or properties, wear resistance, strippability, etc.
- Suitable strip agents include compositions containing phenyl alcohols (e.g., benzyl alcohol); glycol ethers (e.g., propylene glycol methyl ether; phenoxy ethanol; phenoxy propanol; and Ethyl CarbitolTM, Butyl CarbitolTM and Butyl CellosolveTM, all available from Union Carbide Corp.); metasilicates; alkanolamines (e.g., monoethanolamine); and caustic agents such as sodium or potassium hydroxide.
- Compositions containing phenyl alcohols are preferred for laminate finishes employing acrylate or urethane topcoats owing to the relatively high rate at which phenyl alcohols penetrate such topcoats and their ease of use and low odor.
- a particularly preferred strip agent concentrate contains a polar solvent that is denser than water, and a sufficiently low level of cosolvent or surfactant so that upon mixing with water a pseudo-stable aqueous dispersion forms which will phase-separate following application to a surface.
- Another preferred strip agent concentrate contains about 1 to 75 wt. percent of an ether alcohol solvent having a solubility in water of less than about 5 wt. % of the solvent. and about 1 to 75 wt. % of an ether alcohol solvent/coupler having a solubility in water of about 20 to about 100 wt. % of the solvent/coupler, wherein the vapor pressure of the concentrate is less than 1 millimeter Hg.
- Concentrates of this type are described in copending application Ser. No. 09/383,000 filed Aug. 25, 1999, the disclosure of which is incorporated by reference.
- Suitable commercially available strip agents include HawkTM, FreedomTM and Care Strip Low OdorTM stripper concentrates from Ecolab, Inc.; JuggernautTM stripper concentrate from Buckeye International, Inc.; Fuller 3100TM Super Concentrate from H. B. Fuller, Inc. and Twist and FillTM stripper concentrate from 3M.
- the intermediate coating, topcoat and strip agent can contain a variety of adjuvants to alter the performance of properties of each component before or after application to a substrate.
- adjuvants include leveling agents and other surface-active agents, defoamers, solvents to accelerate or to slow the drying rate, waxes, fillers, indicators and colorants. They types and amounts of such adjuvants will be apparent to those skilled in the art.
- compositions of the invention can be applied using a variety of methods, including spraying, brushing, roll coating and flood coating. Mop application is preferred for coating floors. Typically the substrate should first be cleaned and any loose debris removed. One or more coats of the intermediate coating (diluted if necessary with water or another suitable solvent) are applied to the substrate, and allowed to dry. Three to five coats of the intermediate coating topically will be preferred for coating floors. When used on floors, each coat of the intermediate coating preferably will have a dry coating thickness of about 2.5 to about 75 micrometers, more preferably about 2.5 to about 20 micrometers, and the overall intermediate dry coating thickness preferably will be about 5 to about 38 micrometers, more preferably about 5 to about 20 micrometers.
- each coat of the topcoat preferably will have a dry coating thickness of about 2.5 to about 75 micrometers, more preferably about 2.5 to about 20 micrometers, and the overall topcoat dry coating thickness preferably will be about 5 to about 38 micrometers, more preferably about 5 to about 20 micrometers.
- the laminate finish preferably will have an overall dry coating thickness of about 10 to about 75 micrometers, more preferably about 12 to about 38 micrometers.
- the laminate finish composition can thereafter receive normal maintenance until such time as it is desired to remove and renew the laminate finish.
- the laminate finish can be stripped by optionally abrading the topcoat with a suitably mild abrasive (e.g., a green or black Scotch-BriteTM Floor Maintenance pad from 3M) and then applying a coating of the desired strip agent.
- the strip agent should be allowed to stand for a suitable time (e.g., for a minute or more, and typically between about 5 and about 15 minutes) while it permeates through the topcoat and attacks the intermediate coating.
- the substrate can be allowed to dry and new layers of the intermediate coat and topcoat can be applied to renew the laminate finish.
- compositions of the invention typically will be sold in the form of a kit containing the intermediate coating and topcoat in containers (e.g., separate containers) together with suitable directions for carrying out the methods of the invention.
- the intermediate coating or topcoat could be packaged as concentrates intended to be typically will be mixed with water or another suitable solvent at about a 15-40% solids level.
- the kit will include a container of the strip agent.
- the strip agent typically will be mixed with water or another suitable solvent at about a 5-30% by weight.
- the kit can also contain undercoat materials (e.g., leveling coatings) that can be applied to the substrate before application of the intermediate coating, and overcoat materials (e.g., wax finishes) that can be applied atop the topcoat.
- a set of 150 mm square white or black vinyl composite floor tiles from Armstrong Tile or from American Biltrite Limited were coated with 2 coats of a waterborne metal-catalyzed acrylic floor finish (Gemstar LaserTM, Ecolab Inc.) applied at a 20% solids level. Tiles coated only with this acrylic floor finish can readily be stripped in less than 30 minutes using all of the Test Strip Agents listed below.
- Each coat was allowed to air dry before application of the second coat. The total coating thickness after the second coat had dried was about 10 micrometers (at 5 micrometers per coat).
- This first set of coated tiles and a second set of uncoated tiles were next coated with various waterborne UV curable coating formulations.
- the UV curable coating formulations were applied at a 30% solids level with each coat being allowed to air dry before application of the next coat.
- Two coats of the UV curable coating formulation were applied to each of the metal-catalyzed acrylic floor finish coated tiles in the first set.
- the total dried coating thickness for these two UV curable coats was about 15 micrometers (at 7.5 micrometers per coat), yielding a combined coating thickness of about 25 micrometers.
- Three coats of the UV curable coating formulation were applied to each of the uncoated tiles in the second set.
- the total dried coating thickness for these three UV curable coats was about 22.5 micrometers (at 7.5 micrometers per coat).
- Test Strip Agents Aqueous solutions of the following.
- Test Strip Agents diluted with deionized water were used in the examples: Test Strip Agent A: Concentrate 1 at 1:9 dilution (10% in water) Test Strip Agent B: Concentrate 2 at 1:9 dilution (10% in water); formed a clear solution Test Strip Agent C: Concentrate 2 at 1:4 dilution (20% in water); formed a cloudy solution Test Strip Agent D: Concentrate 3 at 1:9 dilution (10% in water) Test Strip Agent E: Concentrate 3 at 1:4 dilution (20% in water) Test Strip Agent F: Concentrate 4 at 1:9 dilution (10% in water) Test Strip Agent G: Concentrate 4 at 1:5 dilution (20% in water) Test Strip Agent H: Concentrate 5 at 1:9 dilution (10% in water) Test Strip Agent I: Concentrate 5 at 1:4 dilution (20% in water) Test Strip Agent J: Concentrate 1 at 1:4 dilution (20% in water) Test Strip Agent K: Dilute solution 6 Test Strip Agent L: Concentr
- Coated tiles were placed on a level surface and flooded with a sufficient quantity of a 10% aqueous solution of Test Strip Agent A to form a 50 mm diameter circular pool on the surface of each coated tile.
- the Test Strip Agent solution was allowed to remain on the tiles for approximately 20 minutes.
- a nonwoven abrasive scrub pad (Scotch-BriteTM green abrasive, 3M) was used make 10 circular rubs on each tile.
- the tiles were rinsed with tap water, blotted dry and rated according to the following scale:
- a 50 mm diameter by 38 mm high carbon steel cylinder with a weight of 571 grams was wrapped with a green nonwoven pad (Scotch-BriteTM Floor Maintenance Disc, 3M).
- the cylinder exerted a pressure of 2.8 kPa and mimicked the pressure applied by a standard electric floor burnisher.
- the coated tiles were placed on a level surface and flooded with a sufficient quantity of a 15% aqueous solution of various Test Strip Agents to form a 50 mm diameter circular pool on the surface of the coated tiles.
- the Strip Agent solution was allowed to remain on the coated tiles for 10 minute or 20 minute standing times.
- the cylinder was then rolled 10 times over each tile.
- the tiles were rinsed with tap water, blotted dry and rated according to the following scale:
- Example 2 Using the method of Example 1, a waterborne UV curable coating formulation obtained from UV Coatings Limited (identified as “936-66-2”, a 75:25 blend of an aliphatic polyester urethane and an acrylic resin) was applied as a topcoat to vinyl composite tiles, with and without a strippable intermediate coating composition between the tile and the topcoat. Using the Second Strippability Evaluation Method (7 Point Scale), the coatings were evaluated for strippability. Test Strip Agents B and C were employed for 10 minute or 30 minute standing times. The results are set out below in Table 2. TABLE 2 Intermediate Test Strip Standing 7 Point Scale Run No. coating?
- Two waterborne UV curable coating formulations were prepared from the ingredients set out below in Table 3: TABLE 3 Formulation Formulation Ingredient A, Parts B, Parts VIAKTIN TM VTE 6165 resin 1 42.86 VIAKTIN TM VTE 6169 resin 2 42.86 Irgacure 500 photoinitiator 3 1.57 1.57 Wax 325 polymer emulsion 4 1.05 0.53 Wax 43N polymer emulsion 4 1.05 1.58 PI-35 defoamer 5 0.1 0.1 FC-120 fluorosurfactant 6 0.05 0.05 Deionized water 53.32 53.32
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Abstract
A coated substrate comprises a strippable intermediate coating on a substrate, and a strip agent-permeable coating or topcoat on the intermediate coating. The topcoat is less strippable and more wear-resistant than the intermediate coating. In a preferred embodiment, the substrate comprises a floor, the topcoat comprises a UV curable floor finish, the intermediate coating comprises a metal-crosslinked acrylic, and the strip agent comprises a chemical strip agent containing a phenyl alcohol.
When the topcoat eventually becomes worn and must be renewed, a strip agent (e.g., chemical strip agent) can be applied to the topcoat. The strip agent penetrates the topcoat and attacks the intermediate coating, thereby enabling removal of the intermediate coating and topcoat without aggressive removal techniques such as sanding.
Certain laminate finishes, strip agents, methods for using these finishes and strip agents; and methods for removing a multilayer laminate finish are used to prepare and to renew the coated substrate.
Description
- This invention relates to a strippable laminate finish, a strippable laminate finish kit, and methods for applying and for removing a finish.
- UV light curable coating compositions typically provide a desirable combination of properties including rapid cure, high gloss and good durability. Due to these properties and their generally good scratch and detergent resistance, UV light curable coating compositions have been used as floor finishes. Eventually even a UV light cured floor finish will show the effects of wear, and will require removal and renewal. UV cured floor finishes generally are not regarded as being removable using conventional chemical floor stripping agents. Instead, more aggressive removal techniques such as floor sanding or aggressive burnishing may be employed, thereby leading to removal of a portion of the underlying floor surface. This has discouraged the use of UV cured floor finishes.
- The present invention provides, in one aspect, a coated substrate comprising a strippable intermediate coating atop the substrate, and a strip agent-permeable coating atop the intermediate coating, wherein the strip agent-permeable coating is less strippable and more wear-resistant than the intermediate coating. In a preferred embodiment, the substrate comprises a floor, the strip agent-permeable coating comprises a UV curable floor finish, the intermediate coating comprises a metal-crosslinked acrylic, and the strip agent comprises a chemical strip agent containing a phenyl alcohol.
- The strip agent-permeable coating (which in the interest of brevity could be referred to as the topcoat, even though it may itself be overcoated with one or more other layers) protects the underlying intermediate coating and substrate from abrasion, dirt, and other environmental effects. When the topcoat eventually becomes worn and must be renewed, a strip agent (e.g., chemical strip agent) can be applied to the topcoat whereupon the strip agent will penetrate the topcoat and attack the underlying intermediate coating. The intermediate coating breaks down due to the action of the strip agent, thereby enabling removal of the intermediate coating and topcoat without the need for the use of aggressive removal techniques such as floor sanding or aggressive burnishing.
- In another aspect, the invention provides a strippable laminate finish kit, comprising one or more containers of a strippable intermediate coating and a strip agent-permeable topcoat, wherein the topcoat is less strippable and more wear resistant than the intermediate coating. The strippable laminate finish kit optionally includes a strip agent.
- In a further aspect, the invention provides a strip agent concentrate containing a polar solvent that is denser than water, and a sufficiently low level of cosolvent or surfactant so that upon mixing with water a pseudo-stable aqueous dispersion forms which will phase-separate following application to a surface.
- In a further aspect, the invention provides a method for applying a finish to a substrate, comprising the steps of applying to the substrate a strippable intermediate coating, allowing the intermediate coating to dry or harden, and applying a strip agent-permeable topcoat to the intermediate coating, wherein the topcoat is less strippable and more wear resistant than the intermediate coating.
- In yet a further aspect, the invention provides a method for removing a multilayer laminate finish having a topcoat and an intermediate later atop a substrate, comprising the steps of applying to the topcoat a strip agent (e.g., a chemical strip agent), allowing the strip agent to permeate through the topcoat to attack the intermediate layer, and removing the intermediate layer and topcoat by mopping, vacuuming, mild abrasion or other measures that do not remove substantial portions of the underlying substrate.
- FIG. 1 shows a view in cross-section of a floor coated with a laminate finish of the invention.
- FIG. 2 shows a view in cross-section of a wall coated with a laminate finish of the invention.
- FIG. 3 shows a view in cross-section of the application of a chemical strip agent to a laminate finish in the invention.
- FIG. 4 shows a view in cross-section illustrating removal of a laminate finish of the invention.
- As used in connection with this invention, a coating is regarded as being “strippable” if when subjected to the action of a suitable strip agent, the coating can readily be removed from the substrate using simple, non-abrasive measures such as a mop and detergent solution, or mildly abrasive but substrate-non-damaging measures such as a nonwoven floor scrub pad. Strippability preferably is evaluated using the Second Strippability Evaluation Method (7 point scale) set out below in the Example section, using Test Strip Agent K and a 10 minute strip agent standing time.
- As used in connection with this invention, a topcoat is regarded as being “strip agent-permeable” if when coated atop the desired strippable coating and subjected to the action of a suitable strip agent, the strip agent permeates or otherwise penetrates the topcoat sufficiently so that the both the topcoat and strippable coating can be removed from the substrate. Strip agent permeability can be enhanced by a mechanically roughening the topcoat (using, for example, a nonwoven floor scrub pad, brush or other mild abrasive measure) just prior to stripping. A topcoat will be regarded as being strip agent-permeable even if such mechanical roughening is required, so long as the required mechanical roughening does not damage the underlying substrate.
- As used in connection with this invention, a topcoat is regarded as being more wear resistant than an underlying strippable intermediate coating when the topcoat exhibits lower weight loss than the underlying intermediate coating using a Taber Abrasion test conducted according to ASTM D4060-95.
- Referring now to FIG. 1.
floor 10 is overcoated withlaminate finish 11 containingintermediate coating 12 andtopcoat 14. Topcoat 14 is a UV-curable floor finish whose wear resistance and durability protect underlyingintermediate coating 12 andfloor 10 from dirt, scuffing and other environmental factors.Intermediate coating 12 is a metal-catalyzed acrylic floor finish having lower wear resistance thantopcoat 14. If used alone onfloor 10,intermediate coating 12 could readily be stripped fromfloor 10 using a conventional chemical floor stripping agent. If used alone onfloor 10,topcoat 12 would not be strippable (or might only be stripped with difficulty) fromfloor 10 using such a stripping agent. - FIG. 2 shows a
wall 20 overcoated withwallpaper 22 andprotective laminate finish 24 containingintermediate coating 26 andtopcoat 28. Topcoat 28 is an acrylic latex paint whose wear resistance and durability protect underlyingintermediate coating 26.wallpaper 22 andwall 20 from scuffing, abrasion and other wear or damage.Intermediate coating 26 is a metal-catalyzed acrylic coating having lower wear resistance thantopcoat 28. If used alone onwall 20,intermediate coating 22 could readily be stripped fromwall 20 using a thickened version of a conventional chemical floor stripping agent. If used alone onwall 20,topcoat 24 would not be strippable (or might only be stripped with difficulty) fromwall 20 using such a stripping agent. - FIG. 3 shows the application of
chemical stripping agent 30 to thelaminate finish 11 of FIG. 1, and FIG. 4 shows the subsequent removal of the softenedlaminate finish 11. As shown in FIG. 3,agent 30 permeates and penetratestopcoat 14 but does not significantly soften or otherwise attacktopcoat 14. On reachingintermediate coating 12.agent 30 causesintermediate coating 12 to soften and break apart.Intermediate coating 12 loosens its bond withfloor 10 and begins a gradual disintegration process (illustrated in FIG. 4) that eventually causesintermediate coating 12 andtopcoat 14 to break up into small particles such asparticles mop 46 andwater 47, the disintegration process can be accelerated.Vacuum 48 facilitates removal of the residue of thelaminate finish 11 fromfloor 12. - A variety of substrates can be coated with the laminate finishes of the invention. For example, flooring materials that can be coated include resilient materials such as vinyl flooring, vinyl composite flooring, and synthetic sports floors; and non-resilient materials such as concrete, marble and wood. Other substrates that can be coated include walls, ceilings, labels, emblems, indoor and outdoor signs, and vehicles such as automobiles.
- A variety of intermediate coating materials can be employed. Suitable intermediate coating materials should be strippable using a strip agent that is capable of permeating the topcoat. Thus, the choice of intermediate coating material will be determined in part by the chosen topcoat and stripping agent. Waterborne intermediate coatings materials are preferred for ease of application. Water-soluble acid-containing polymers crosslinked using transition metals (e.g., metal crosslinked acrylics) are a particularly preferred class of intermediate coating materials. These can be stripped using a variety of strip agents (described in more detail below) that dissolve the intermediate coating or attack the crosslinking site. Preferred intermediate coatings will have a rating of 6 or more, more preferably a rating of 7, when coated alone on a vinyl composite tile substrate and evaluated using second Strippability Evaluation Method (7 point scale), using Test Strip Agent K and a 10 minute strip agent standing time. Suitable commercially available metal crosslinked acrylic polymers include Gemstar Laser™ and Taj Mahal™ acrylic finishes from Ecolab Inc.; High Noon™ acrylic finish from Butchers; Citation™ acrylic finish from Buckeye International, Inc., Signature™, Vectra™, and Complete™ acrylic finishes from SC Johnson Professional Products; Upper Limits™ acrylic finish from Spartan Chemical Co.; and materials such as those described in U.S. Pat. Nos. 4,517,330 and 5,319,018 and the patents cited therein. Strippable floor coatings designated as “sealers” (e.g., Over and Under™ floor sealer, available from S. C. Johnson Professional Products) and strippable coatings based on polyvinylacetates could also be used. If desired, two or more layers of different intermediate coatings can be employed in laminate finishes of the invention, in order to optimize properties such as adhesion to the substrate or to the topcoat, wear resistance, strippability, etc.
- A variety of topcoat materials can be used in the invention. Suitable topcoat materials should be less strippable than the intermediate coating, and should be permeable by a chemical strip agent that is capable of stripping the intermediate coating material. Thus, the choice of topcoat material will be determined in part by the chosen intermediate coating material and stripping agent. Preferred topcoat materials will have a rating of 5 or less, and more preferably a rating of 3 or less, if coated alone on a vinyl composite tile substrate and evaluated using the second Strippability Evaluation Method (7 point scale), Test Strip Agent K and a 10 minute strip agent standing time. When the intermediate coating and topcoat are each coated alone and compared using such an evaluation method, they preferably will have at least a 1 point differential, more preferably at least a 2 point differential, and most preferably at least a 4 point differential in observed strippability rating values.
- Polymerizable topcoat materials (e.g. two-part thermally curable or one-part photocurable materials) are preferred due to their durability. In addition, topcoat materials that are waterborne or otherwise substantially solvent free (e.g., 100 percent solids low viscosity formulations) are preferred for environmental reasons. Preferably the topcoat is not metal crosslinked. Suitable topcoat materials include urethanes, acrylics, epoxies, melamines and blends or copolymers thereof. Waterborne UV curable acrylates and urethanes are particularly preferred topcoat materials. These tend to be less strippable and more wear resistant than the metal crosslinked acrylic intermediate coatings mentioned above, and are permeable by strip agents that can be used to remove such intermediate coating materials. Suitable commercially or experimentally available topcoat materials include UV curable acrylates, urethanes and urethane acrylates (including aliphatic polyester urethane acrylates) such as the materials designated as 935-63 through 935-67; 935-75B; 935-76 and 935-80 through 935-82 series of UV curable coatings from UV Coatings Limited; RoShield™ 3120 UV curable acrylate coating from Rohm & Haas; and NeoRad™ NR-3709 UV curable aliphatic urethane coating from Zeneca Resins, and materials such as those described in U.S. Pat. Nos. 5,453,451 and 5,773,487. A variety of other coating resins that can be cured using suitable crosslinking agents, thermal initiators or photoinitiators can be employed, including Courtmaster II™ waterborne acrylic urethane available from Ecolab, Inc.; Laromer™ PE 55W polyester acrylate, LR 8895 polyester acrylate, LR 8949 aliphatic urethane and LR 8983 aromatic urethane waterborne acrylic ester resins, all available from BASF Corp.; Viaktin™ VTE 6155 aliphatic urethane acrylate. VTE 6165 aromatic urethane acrylate and VTE 6169 aliphatic polyester urethane radiation curing resins, all available from Vianova Resins GmbH & Co. KG; 98-283W urethane acrylate, available from Hans Rahn & Co.; and materials such as those described in U.S. Pat. No. 5,830,937. If desired, two or more layers of different topcoats can be employed in laminate finishes of the invention, in order to optimize properties such as adhesion to the intermediate coating, laminate surface appearance or properties, wear resistance, strippability, etc.
- Suitable strip agents include compositions containing phenyl alcohols (e.g., benzyl alcohol); glycol ethers (e.g., propylene glycol methyl ether; phenoxy ethanol; phenoxy propanol; and Ethyl Carbitol™, Butyl Carbitol™ and Butyl Cellosolve™, all available from Union Carbide Corp.); metasilicates; alkanolamines (e.g., monoethanolamine); and caustic agents such as sodium or potassium hydroxide. Compositions containing phenyl alcohols are preferred for laminate finishes employing acrylate or urethane topcoats owing to the relatively high rate at which phenyl alcohols penetrate such topcoats and their ease of use and low odor.
- A particularly preferred strip agent concentrate contains a polar solvent that is denser than water, and a sufficiently low level of cosolvent or surfactant so that upon mixing with water a pseudo-stable aqueous dispersion forms which will phase-separate following application to a surface.
- Another preferred strip agent concentrate contains about 1 to 75 wt. percent of an ether alcohol solvent having a solubility in water of less than about 5 wt. % of the solvent. and about 1 to 75 wt. % of an ether alcohol solvent/coupler having a solubility in water of about 20 to about 100 wt. % of the solvent/coupler, wherein the vapor pressure of the concentrate is less than 1 millimeter Hg. Concentrates of this type are described in copending application Ser. No. 09/383,000 filed Aug. 25, 1999, the disclosure of which is incorporated by reference.
- Suitable commercially available strip agents include Hawk™, Freedom™ and Care Strip Low Odor™ stripper concentrates from Ecolab, Inc.; Juggernaut™ stripper concentrate from Buckeye International, Inc.; Fuller 3100™ Super Concentrate from H. B. Fuller, Inc. and Twist and Fill™ stripper concentrate from 3M.
- The intermediate coating, topcoat and strip agent can contain a variety of adjuvants to alter the performance of properties of each component before or after application to a substrate. Useful adjuvants include leveling agents and other surface-active agents, defoamers, solvents to accelerate or to slow the drying rate, waxes, fillers, indicators and colorants. They types and amounts of such adjuvants will be apparent to those skilled in the art.
- The compositions of the invention can be applied using a variety of methods, including spraying, brushing, roll coating and flood coating. Mop application is preferred for coating floors. Typically the substrate should first be cleaned and any loose debris removed. One or more coats of the intermediate coating (diluted if necessary with water or another suitable solvent) are applied to the substrate, and allowed to dry. Three to five coats of the intermediate coating topically will be preferred for coating floors. When used on floors, each coat of the intermediate coating preferably will have a dry coating thickness of about 2.5 to about 75 micrometers, more preferably about 2.5 to about 20 micrometers, and the overall intermediate dry coating thickness preferably will be about 5 to about 38 micrometers, more preferably about 5 to about 20 micrometers.
- Next, one or more coats of the topcoat (diluted if necessary with water or another suitable solvent) can be applied to the intermediate coating as soon as the intermediate coating has dried to the touch. The topcoat is applied, and cured or allowed to dry or harden. Three to five coats of the topcoat typically will be preferred for coating floors. When used on floors, each coat of the topcoat preferably will have a dry coating thickness of about 2.5 to about 75 micrometers, more preferably about 2.5 to about 20 micrometers, and the overall topcoat dry coating thickness preferably will be about 5 to about 38 micrometers, more preferably about 5 to about 20 micrometers. When used on floors, the laminate finish preferably will have an overall dry coating thickness of about 10 to about 75 micrometers, more preferably about 12 to about 38 micrometers.
- The laminate finish composition can thereafter receive normal maintenance until such time as it is desired to remove and renew the laminate finish. The laminate finish can be stripped by optionally abrading the topcoat with a suitably mild abrasive (e.g., a green or black Scotch-Brite™ Floor Maintenance pad from 3M) and then applying a coating of the desired strip agent. The strip agent should be allowed to stand for a suitable time (e.g., for a minute or more, and typically between about 5 and about 15 minutes) while it permeates through the topcoat and attacks the intermediate coating. After the finish softens sufficiently, it can be removed using a variety of techniques including vacuuming, mopping or wiping. Removal will usually be made easier if water or a suitable detergent solution is applied to the softened finish. The substrate can be allowed to dry and new layers of the intermediate coat and topcoat can be applied to renew the laminate finish.
- The compositions of the invention typically will be sold in the form of a kit containing the intermediate coating and topcoat in containers (e.g., separate containers) together with suitable directions for carrying out the methods of the invention. If desired, the intermediate coating or topcoat could be packaged as concentrates intended to be typically will be mixed with water or another suitable solvent at about a 15-40% solids level. Optionally the kit will include a container of the strip agent. The strip agent typically will be mixed with water or another suitable solvent at about a 5-30% by weight. The kit can also contain undercoat materials (e.g., leveling coatings) that can be applied to the substrate before application of the intermediate coating, and overcoat materials (e.g., wax finishes) that can be applied atop the topcoat.
- The invention is further illustrated in the following non-limiting examples, in which all parts and percentages are by weight unless otherwise indicated. In the examples the following procedures were employed:
- A set of 150 mm square white or black vinyl composite floor tiles from Armstrong Tile or from American Biltrite Limited were coated with 2 coats of a waterborne metal-catalyzed acrylic floor finish (Gemstar Laser™, Ecolab Inc.) applied at a 20% solids level. Tiles coated only with this acrylic floor finish can readily be stripped in less than 30 minutes using all of the Test Strip Agents listed below. Each coat was allowed to air dry before application of the second coat. The total coating thickness after the second coat had dried was about 10 micrometers (at 5 micrometers per coat). This first set of coated tiles and a second set of uncoated tiles were next coated with various waterborne UV curable coating formulations. The UV curable coating formulations were applied at a 30% solids level with each coat being allowed to air dry before application of the next coat. Two coats of the UV curable coating formulation were applied to each of the metal-catalyzed acrylic floor finish coated tiles in the first set. The total dried coating thickness for these two UV curable coats was about 15 micrometers (at 7.5 micrometers per coat), yielding a combined coating thickness of about 25 micrometers. Three coats of the UV curable coating formulation were applied to each of the uncoated tiles in the second set. The total dried coating thickness for these three UV curable coats was about 22.5 micrometers (at 7.5 micrometers per coat). Thus the two sets of tiles were coated to nearly similar overall thicknesses, at 25 micrometers for the tiles in the first set and 22.5 micrometers thickness for the tiles in the second set. Both sets of tiles were passed through a UV curing apparatus containing an H bulb mercury vapor lamp operated at 1935 joule/sec per cm2 and 4.9 meters per minute.
Test Strip Agents Aqueous solutions of the following. Test Strip Agents diluted with deionized water were used in the examples: Test Strip Agent A: Concentrate1 at 1:9 dilution (10% in water) Test Strip Agent B: Concentrate2 at 1:9 dilution (10% in water); formed a clear solution Test Strip Agent C: Concentrate2 at 1:4 dilution (20% in water); formed a cloudy solution Test Strip Agent D: Concentrate3 at 1:9 dilution (10% in water) Test Strip Agent E: Concentrate3 at 1:4 dilution (20% in water) Test Strip Agent F: Concentrate4 at 1:9 dilution (10% in water) Test Strip Agent G: Concentrate4 at 1:5 dilution (20% in water) Test Strip Agent H: Concentrate5 at 1:9 dilution (10% in water) Test Strip Agent I: Concentrate5 at 1:4 dilution (20% in water) Test Strip Agent J: Concentrate1 at 1:4 dilution (20% in water) Test Strip Agent K: Dilute solution6 Test Strip Agent L: Concentrate7 at 1:4 dilution (20% in water) - Coated tiles were placed on a level surface and flooded with a sufficient quantity of a 10% aqueous solution of Test Strip Agent A to form a 50 mm diameter circular pool on the surface of each coated tile. The Test Strip Agent solution was allowed to remain on the tiles for approximately 20 minutes. Using light and consistent pressure, a nonwoven abrasive scrub pad (Scotch-Brite™ green abrasive, 3M) was used
make 10 circular rubs on each tile. The tiles were rinsed with tap water, blotted dry and rated according to the following scale: - 1) No effect
- 2) Chemical attack on surface (non tacky)
- 3) Slight removal in spots or abrasion (random scratches on the surface of the coating)
- 4) Incomplete strip (may strip completely in some areas, especially where topcoat was porous, but not in other areas. Coating is slightly soft or tacky)
- 5) Partial strip with softened coating in all areas
- 6) Complete strip
- A 50 mm diameter by 38 mm high carbon steel cylinder with a weight of 571 grams was wrapped with a green nonwoven pad (Scotch-Brite™ Floor Maintenance Disc, 3M). When rolled over a coated tile substrate, the cylinder exerted a pressure of 2.8 kPa and mimicked the pressure applied by a standard electric floor burnisher. The coated tiles were placed on a level surface and flooded with a sufficient quantity of a 15% aqueous solution of various Test Strip Agents to form a 50 mm diameter circular pool on the surface of the coated tiles. The Strip Agent solution was allowed to remain on the coated tiles for 10 minute or 20 minute standing times. The cylinder was then rolled 10 times over each tile. The tiles were rinsed with tap water, blotted dry and rated according to the following scale:
- 1) No effect
- 2) Minimal chemical attack on coating
- 3) Moderate chemical attack on coating
- 4) Severe chemical attack on coating with onset of stripping
- 5) Incomplete strip (may strip completely in some areas, especially where coating was porous, but not in other areas. Finish is slightly soft or tacky)
- 6) Partial strip with softened finish in all areas
- 7) Complete strip
- Using the First Strippability Evaluation Method (6 Point Scale) set out above, several waterborne UV curable coating formulations obtained from UV Coatings Limited were applied to tiles and evaluated for strippability with and without the use of a strippable intermediate coating composition between the tile and the topcoat. The results are set out below in Table 1.
TABLE 1 Intermediate 6 Point Scale Run No. coating? Overcoat Evaluation 1-1 No 935-62 1 1-2 Yes 935-62 3 1-3 No 935-63 1 1-4 Yes 935-63 4 1-5 No 935-64 3 1-6 Yes 935-64 5 1-7 No 935-65 4 1-8 Yes 935-65 5 1-9 Yes 935-651 5 - The results in Table 1 show that for each of the tested UV curable topcoat formulations, strippability was improved hen the intermediate coat was present.
- Using the method of Example 1, a waterborne UV curable coating formulation obtained from UV Coatings Limited (identified as “936-66-2”, a 75:25 blend of an aliphatic polyester urethane and an acrylic resin) was applied as a topcoat to vinyl composite tiles, with and without a strippable intermediate coating composition between the tile and the topcoat. Using the Second Strippability Evaluation Method (7 Point Scale), the coatings were evaluated for strippability. Test Strip Agents B and C were employed for 10 minute or 30 minute standing times. The results are set out below in Table 2.
TABLE 2 Intermediate Test Strip Standing 7 Point Scale Run No. coating? Agent Time, min Evaluation 2-1 No B 10 2 2-2 Yes B 10 7 2-3 No B 30 3 2-4 Yes B 30 7 2-5 No C 10 5 2-6 Yes C 10 7 2-7 No C 30 4 2-8 Yes C 30 7 2-9 No D 10 1 2-10 Yes D 10 1 2-11 No D 30 1 2-12 Yes D 30 5 2-13 No E 10 1 2-14 Yes E 10 2 2-15 No E 30 1 2-16 Yes E 30 7 2-17 No F 10 2 2-18 Yes F 10 6 2-19 No F 30 2 2-20 Yes F 30 7 2-21 No G 10 3 2-22 Yes G 10 6 2-23 No G 30 3 2-24 Yes G 30 7 2-25 No H 10 4 2-26 Yes H 10 6 2-27 No H 30 4 2-28 Yes H 30 7 2-29 No I 10 4 2-30 Yes I 10 6 2-31 No I 30 4 2-32 Yes I 30 7 2-33 No A 10 1 2-34 Yes A 10 1 2-35 No A 30 1 2-36 Yes A 30 2 2-37 No J 10 1 2-38 Yes J 10 1 2-39 No J 30 1 2-40 Yes J 30 4 - The results in Table 2 show that for each of the tested UV curable topcoat formulations, strippability was improved when the intermediate coat was present. The laminate finish formulations were completely strippable with most of the Test Strip Agents, whereas the corresponding topcoat was not completely strippable with any of the Test Strip Agents. Complete stripping of the laminate finish formulations was achieved in less than 6 minutes using Test Strip Agent B, and in less than 1 minute using Test Strip Agent C.
- Two waterborne UV curable coating formulations were prepared from the ingredients set out below in Table 3:
TABLE 3 Formulation Formulation Ingredient A, Parts B, Parts VIAKTIN ™ VTE 6165 resin1 42.86 VIAKTIN ™ VTE 6169 resin2 42.86 Irgacure 500 photoinitiator3 1.57 1.57 Wax 325 polymer emulsion4 1.05 0.53 Wax 43N polymer emulsion4 1.05 1.58 PI-35 defoamer5 0.1 0.1 FC-120 fluorosurfactant6 0.05 0.05 Deionized water 53.32 53.32 - Using the method of Example 1, these compositions were applied as topcoats to vinyl composite tiles, with and without a strippable intermediate coating composition between the tile and the topcoat. Using the Second Strippability Evaluation Method (7 Point Scale), the coatings were evaluated for strippability. Test Strip Agent L was employed for a 10 minute standing time. The results are set out below in Table 4.
TABLE 4 Intermediate 7 Point Scale Run No. coating? Topcoat Test Strip Agent Evaluation 3-1 No A L 2 3-2 Yes A L 7 3-3 No B L 2 3-4 Yes B L 7 - Various modifications and alterations of this invention will be apparent to those skilled in the art without departing from the scope and spirit of this invention. It should be understood that this invention is not limited to the illustrative embodiments set forth above.
Claims (30)
1. A coated substrate comprising a strippable intermediate coating atop the substrate, and a strip agent-permeable coating atop the intermediate coating, wherein the strip agent-permeable coating comprised a waterborne composition and is less strippable and more durable than the intermediate coating.
2. A coated substrate according to claim 1 , wherein the substrate comprises a floor.
3. A coated substrate according to claim 2 , wherein the substrate comprises a resilient flooring material.
4. A coated substrate according to claim 3 , wherein the substrate comprises a vinyl or vinyl composite tile.
5. A coated substrate according to claim 1 , wherein the substrate comprises a wall, ceiling, label, emblem, sign or vehicle.
6. A coated substrate according to claim 1 , wherein the intermediate coating comprises a metal-catalyzed acrylic finish.
7. A coated substrate according to claim 1 , wherein the intermediate coating has a strippability rating of 6 or more on a 7 point scale, corresponding to at least partial strip with softened finish in all areas, using a test strip agent made using a 25% water solution of a concentrate that contained 59% softened water, 6% sodium xylene sulfonate, 4.5% potassium hydroxide, 10% monoethanolamine, 0.2% tetrasodium EDTA, 10% ethylene glycol phenyl ether and 0.05% fluorosurfactant, and a 10 minute standing time.
8. A coated substrate according to claim 1 , wherein the intermediate coating has a thickness of about 5 to about 38 micrometers.
9. A coated substrate according to claim 1 , wherein the topcoat comprises a polymerized material.
10. A coated substrate according to claim 1 , wherein the topcoat comprised a one-part photopolymerizable material.
11. A coated substrate according to claim 1 , wherein the topcoat comprised a UV curable material.
12. A coated substrate according to claim 1 , wherein the topcoat comprises an acrylate, urethane or acrylated urethane.
13. A coated substrate according to claim 12 , wherein the topcoat comprises an aromatic urethane.
14. A coated substrate according to claim 12 , wherein the topcoat comprises an aliphatic polyester urethane.
15. A coated substrate according to claim 1 , wherein the topcoat is not metal crosslinked.
16. A coated substrate according to claim 1 , wherein the topcoat has a strippability rating of 4 or less on a 7 point scale, corresponding to no more than severe chemical attack on the topcoat and the onset of stripping, using a test strip agent made using a 25% water solution of a concentrate that contained 59% softened water, 6% sodium xylene sulfonate, 4.5% potassium hydroxide, 10% monoethanolamine, 0.2% tetrasodium EDTA, 10% ethylene glycol phenyl ether and 0.05% fluorosurfactant, and a 10 minute standing time.
17. A coated substrate according to claim 1 , wherein the topcoat has a thickness of about 5 to about 38 micrometers.
18. A coated substrate according to claim 1 , wherein the intermediate coating or topcoat comprise two or more different layers of materials.
19. A coated substrate according to claim 1 , wherein the substrate comprises a floor and the strip agent-permeable coating comprises a UV curable finish.
20-30 cancelled.
31. A method for applying a finish to a substrate, comprising:
a) applying to the substrate a strippable intermediate coating;
b) allowing the intermediate coating to dry or harden; and
c) applying a strip agent-permeable topcoat to the intermediate coating, wherein the topcoat comprises a waterborne composition and is less strippable and more durable than the intermediate coating.
32. A method according to claim 31 , wherein the topcoat is UV cured.
33. A method according to claim 31 , wherein the intermediate coating is applied in two or more coats.
34. A method according to claim 31 , wherein the topcoat is applied in two or more coats.
35. A method according to claim 34 , wherein each of said two or more coats is UV cured before application of any further coat.
36. A method for removing a finish from a substrate, comprising:
a) applying a strip agent to a laminate finish comprising a strip agent-permeable coating atop a strippable intermediate coating atop a substrate, wherein the strip agent-permeable coating comprises a waterborne composition and is less strippable and more durable than the intermediate coating;
b) allowing the strip agent to permeate through the topcoat to attack the intermediate layer; and
c) removing the intermediate layer and topcoat without removing substantial portions of the underlying substrate.
37. A method according to claim 36 , wherein permeation of the strip agent through the topcoat is enhanced by a mechanically roughening the topcoat prior to applying the strip agent.
38. A method according to claim 36 , wherein removal of the intermediate layer and topcoat occurs in less than 10 minutes after application of the strip agent.
39. A coated substrate according to claim 1 , wherein the topcoat comprises a urethane.
40. A method according to claim 31 , wherein the topcoat comprises a urethane.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US10/821,560 US20040191484A1 (en) | 2000-04-28 | 2004-04-09 | Strippable laminate finish |
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US56017000A | 2000-04-28 | 2000-04-28 | |
US10/821,560 US20040191484A1 (en) | 2000-04-28 | 2004-04-09 | Strippable laminate finish |
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US56017000A Division | 1999-08-25 | 2000-04-28 |
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US09/838,884 Abandoned US20020028621A1 (en) | 2000-04-28 | 2001-04-20 | Strippable laminate finish |
US10/821,560 Abandoned US20040191484A1 (en) | 2000-04-28 | 2004-04-09 | Strippable laminate finish |
US10/822,120 Abandoned US20040191505A1 (en) | 2000-04-28 | 2004-04-09 | Strippable laminate finish |
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US09/838,884 Abandoned US20020028621A1 (en) | 2000-04-28 | 2001-04-20 | Strippable laminate finish |
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US10/822,120 Abandoned US20040191505A1 (en) | 2000-04-28 | 2004-04-09 | Strippable laminate finish |
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AT (1) | ATE402249T1 (en) |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080280061A1 (en) * | 2007-05-07 | 2008-11-13 | Roger Questel | Method for sealing natural stone |
US20100330372A1 (en) * | 2007-05-17 | 2010-12-30 | Johnsondiversey, Inc. | Surface coating system and method |
US9868862B2 (en) | 2011-05-25 | 2018-01-16 | Diversey, Inc. | Surface coating system and method of using surface coating system |
Also Published As
Publication number | Publication date |
---|---|
US20040191505A1 (en) | 2004-09-30 |
US20020028621A1 (en) | 2002-03-07 |
US6544942B1 (en) | 2003-04-08 |
ATE402249T1 (en) | 2008-08-15 |
DE60134969D1 (en) | 2008-09-04 |
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