USRE36742E - Two component powder coating system and method for coating a heat sensitive substrate therewith - Google Patents

Two component powder coating system and method for coating a heat sensitive substrate therewith Download PDF

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Publication number
USRE36742E
USRE36742E US09/271,388 US27138899A USRE36742E US RE36742 E USRE36742 E US RE36742E US 27138899 A US27138899 A US 27138899A US RE36742 E USRE36742 E US RE36742E
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United States
Prior art keywords
coating
powder
epoxy resin
curing agent
low temperature
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US09/271,388
Inventor
Glenn D. Correll
Andrew T. Daly
Joseph J. Kozlowski
Richard P. Haley
Jeno Muthiah
Paul R. Horinka
Eugene P. Reinheimer
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Rohm and Haas Chemicals LLC
Original Assignee
Correll; Glenn D.
Daly; Andrew T.
Kozlowski; Joseph J.
Haley; Richard P.
Muthiah; Jeno
Horinka; Paul R.
Reinheimer; Eugene P.
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Application filed by Correll; Glenn D., Daly; Andrew T., Kozlowski; Joseph J., Haley; Richard P., Muthiah; Jeno, Horinka; Paul R., Reinheimer; Eugene P. filed Critical Correll; Glenn D.
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/182Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/02Processes for applying liquids or other fluent materials performed by spraying
    • B05D1/04Processes for applying liquids or other fluent materials performed by spraying involving the use of an electrostatic field
    • B05D1/06Applying particulate materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/182Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents
    • C08G59/184Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents with amines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/50Amines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/68Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
    • C08G59/686Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/03Powdery paints
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment 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
    • B05D3/02Pretreatment 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 baking
    • B05D3/0218Pretreatment, e.g. heating the substrate
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment 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
    • B05D3/02Pretreatment 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 baking
    • B05D3/0218Pretreatment, e.g. heating the substrate
    • B05D3/0227Pretreatment, e.g. heating the substrate with IR heaters
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment 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
    • B05D3/02Pretreatment 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 baking
    • B05D3/0254After-treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment 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
    • B05D3/02Pretreatment 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 baking
    • B05D3/0254After-treatment
    • B05D3/0263After-treatment with IR heaters
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31511Of epoxy ether
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/4935Impregnated naturally solid product [e.g., leather, stone, etc.]
    • Y10T428/662Wood timber product [e.g., piling, post, veneer, etc.]

Definitions

  • This invention relates to a two-component powder coating system by which the curing of a coating occurs at a significantly faster rate and/or at a significantly lower temperature and produces an exceptionally smooth surface.
  • This invention also relates to thermally stable powder coating whereby white coatings do not yellow during thermal curing.
  • This invention also relates to the electrostatic coating of metal and, in particular, to the triboelectric coating of wood with a coating powder and low temperature curing of that coating having a pleasing smoothness.
  • coating powders have been made by the extrusion of a mixture of resins and curing agents to obtain a homogeneous mixture and then grinding the extrudate and screening the comminuted product to obtain the desired particle sizes and particle size distribution.
  • the powder is then electrostatically sprayed onto a substrate, traditionally a metal substrate, and cured at temperatures much higher than 200° F.
  • the curing of powder coatings on heat sensitive materials has been limited by the fact that the extrusion of a mixture of a resin and a low temperature curing agent, i.e., one that is active at 200° F. or less, would cause the coating powder to gel in the extruder because the extrusion typically generates enough heat to raise the temperature to 200° F.
  • Boise Cascade shows the use of hand-held electrostatic spray guns in coating its electrically conducting particleboard.
  • the epoxy resin is first extruded with a small amount of catalyst or with a low level of a low temperature curing agent and then ground and classified in the usual manner. Additional amounts of the low temperature curing agent in powder form are then blended with the powdered extrudate raise the level of curing agent while avoiding the pre-gelation problem. Surprisingly, the time required to obtain a smooth cured film is lowered significantly. It was surprising, also, that a low gloss film was achieved at cure temperatures much lower than 300° F.
  • thermosetting powder coating system in which the thermosetting of an extruded mixture of a self-curing epoxy resin and (A) a catalyst or (B) an amount of a low temperature curing agent insufficient to cause substantial curing of the resin during extrusion is facilitated by the separate addition of a low temperature curing agent; said extruded mixture and said separately added low temperature curing agent both being in powder form and being blended to form a coating powder.
  • the curing system of this invention may be used in coating glass, ceramics, and graphite-filled composites as well as metallic substrates such as steel and aluminum but its particular utility in the coating of heat sensitive subsrates such as plastics, paper, cardboard and woods makes it highly appealing as a commercially viable alternative to the liquid coatings that have been almost universally used in the past.
  • wood is defined as any lignocellulosic material whether it comes from trees or other plants and whether it be in its natural forms, shaped in a saw mill, separated into sheets and made into plywood, or chipped and made into particleboard, or its fibers have been separated, felted, and compressed.
  • the particle board may be standard or treated to enhance its electrical conductivity. Wood having a moisture content of from 3 to 10% by weight is suitable for the purposes of this invention.
  • a porous particleboard, pre-coated with a conductive liquid coating composition and cured, may also serve as a substrate for the coating powder of this invention. For example, a smooth 2-3 mil thick powder coating is achieved on a 0.5 to 1 mil thick UV or thermally cured pre-coat. Without the precoat, a smooth powder coating must be about 9 mils thick.
  • a particularly favored embodiment of the system is one in which competing reactions are taking place simultaneously, said reactions being:
  • Epoxy resins which are useful in the practice of this invention are exemplified by, but not limited to, those produced by the reaction of epichlorohydrin and a bisphenol, e.g., bisphenol A.
  • Preferred epoxy resins include those sold under the trademarks ARALDITE GT-7072, 7004, 3032, 6062, and 7220, and EPON 1007F, 1009F, and 1004, all of which are 4,4'-isopropylidenediphenolepichlorohydrin resins.
  • the epoxy resin is self-curing, i.e., it reacts via homopolymerization during curing of the powder coating.
  • a catalyst is required to cause the reaction to progress at a commercially acceptable rate.
  • a preferred catalyst for this invention is an epoxy adduct of an imidazole having the general formula: ##STR1## wherein R 1 , R 2 , R 3 , and R 4 are independently hydrogen or any substituent which is not reactive with the epoxy resin.
  • suitable imidazoles include imidazole, 2-methyl imidazole, and 2-phenyl imidazole.
  • Suitable adducts of such imidazoles with a bisphenol A epoxy resin are available commercially from Shell Chemical Company under its trademark EPON, e.g., EPON P-101, and also from Ciba-Geigy Corporation under its designation XU HT 261.
  • EPON e.g., EPON P-101
  • XU HT 261 Ciba-Geigy Corporation
  • imidazole is used herein to mean both the substituted and unsubstituted imidazoles.
  • the adducted imidazole acts as a catalyst, moving from one epoxy group to another as it facilitates epoxy ring opening and cure reactions. Imidazoles, in themselves, tend to be insoluble in epoxy resins. Thus, the purpose for adducting them to an epoxy resin is to make them compatible with the epoxy system.
  • the imidazole adduct is used in the systems, methods, and powders of this invention at a level of from about 0.1 to about 8 parts per hundred parts of the extruded resin (phr), preferably at about 2 phr.
  • the 2-phenyl imidazole may be used as the catalyst for curing the epoxy resin with or without the low temperature curing agent.
  • the 2-phenyl imidazole which is available from the SWK Chemical Co., may be used as such at accordingly lower levels.
  • the imidazoles as adducts or non-adducts, may also used at higher levels as a separately added curing agent to the extruded mixture of the resin and catalyst. When this is done, the amount of imidazole adduct is controlled so that the total amount is no more than about 12 phr.
  • the low temperature curing agent may be selected from among the many that are commercially available but an epoxy adduct of an aliphatic polyamine having a primary amino group is preferable.
  • a suitable curing agent of that type is available from Ciba Ceigy as its PF LMB 5218 hardener.
  • a similar product is sold under the trademark ANCAMINE 2337 XS by Air Products & Chemicals.
  • An epoxy adduct of an aliphatic polyamine having a secondary amino group available under the trademark ANCAMINE 2014 AS is preferred for white and light colored coatings.
  • the amount of low temperature curing agent that may be added separately as component (B) to the pulverized extrudate of resin and catalyst is from about 2 to about 40 phr and the preferred amount is from about 30 to about 35 phr.
  • the ratio of the low temperature curing agent to the catalyst in the extrudate is from about 1:3 to about 400:1 but preferably from about 2:1 to about 15:1.
  • the coating powder may also contain a flow control agent in the range of from about 0.5 to about 2.0 phr.
  • the flow control agents include the MODAFLOW poly (alkylacrylate) products and the SURFYNOL acetylenic diols; they may be used singly or in combination.
  • Anti-oxidants may also be used at a concentration of from about 0.5 to about 2.0 phr to prevent the discoloration of the coatings even at the relatively low curing temperatures suitable for the purposes of this invention.
  • anti-oxidants examples include sodium hypophosphite, tris-(2,4-di-t-butyl phenyl) phosphite (sold under the trademark IRGAFOS 168), and calcium bis([monoethyl(3,5-di-t-butyl-4-hydroxybenzyl)phosphonate] (sold under the trademark IRGANOX 1425). Mixtures of anti-oxidants may be used.
  • Pigments, optical brighteners, fillers such as calcium carbonate and bentonite clays, texturizing agents such as particulate rubber, and other conventional additives may also be present.
  • a particularly desirable textured finish may be obtained by the addition of from about 14 to about 20 phr of the rubber to the coating composition along with calcium carbonate at a rubber to carbonate ratio of from about 0.7:1 to about 1.5:1 by weight.
  • Titanium oxide, in an amount of from about 5 to about 50 phr or more, is an example of a pigment that may be used.
  • An optical brightener exemplified by 2,2'-(2,5-thiophenediyl)bis[5-t-butylbenzoxazole, sold under the trademark UVITEX OB, may be present at from about 0.1 to about 0.5 phr.
  • the term resin includes the resin per se and the crosslinking agent whether it is in the extrudate or it is added separately but it does not include the catalyst.
  • the coating powder of this invention may be applied by any of the conventional powder coating methods but the application of the powder by triboelectric guns is preferred in particular situations such as when the wooden substrate is profiled.
  • the grooves and ridges present a particular problem for electrostatic coating processes because of the Faraday effect. Because the electrical field generated by friction as the powder flows along the TEFLON plastic surfaces inside the gun is relatively small in comparison with the field in a corona-discharge cloud, the powder particles may be deposited more efficiently into Faraday cage areas with triboelectric guns.
  • Wooden cabinet doors are examples of a profiled wooden substrate as are the doorskins represented by the drawings in U.S. Pat No.
  • 5,489,460 which is incorporated herein by reference to further illustrate the type of wooden panels that are particularly susceptible to powder coating by the method of this invention.
  • the grooves and sharp edges of such panels are covered very well on a flat line coating apparatus with nozzles arrayed to direct a portion of the powder against them.
  • Such panels as well as flat-surfaced panels such as those used to make ping-pong tables are particularly well coated by triboelectric guns on a flat line conveyor having electrically conductive bands around the circumference of the conveyor belt.
  • Apparatus for such coating is disclosed in a series of patents assigned to the Nordson Corporation. These are U.S. Pat. Nos. 4,498,913; 4,590,884; 4,723,505; 4,871,380; 4,910,047: and 5,018,909; all of which are incorporated herein by reference.
  • a suitable flat line powder coating apparatus comprises such a conveyor extending through a powder coating booth, wherein a wooden article supported and moved by the conveyor belt is coated triboelectrically by a plurality of guns situated adjacent one another and in one or more tiers.
  • the powder is forced into the guns under about 40 psi pressure and air at about 20 psi is passed into the powder conduits just before the powder passes into the nozzles.
  • the article bearing the powder is then conveyed through a curing oven having several heating zones, some of which are heated by IR lamps, others by heat convection, and still others by a combination of those two.
  • the coating and curing line speeds may be the same or different depending on the the length of the curing oven.
  • the line speed through the powder application booth may be from about 5 to about 150 feet per minute but it is preferably from about 20 to about 100 feet per minute.
  • the line speed through the curing oven may be from about 5 to about 20 feet per minute, depending on the oven temperature and the particular coating powder used.
  • the curing temperature may range from about 180° up to but not including the decomposition temperature of the powder. It is preferred to maintain the cure temperature within the range of from about 190° to about 290° F. and still more preferred to keep the cure temperature at from about 250° to about 290° F. When a crystalline epoxy resin is used, a cure temperature of about 180° F. is particularly suitable. It is preferred that the coating and curing line speeds be adjusted to the oven length so that they are balanced.
  • Preheating of the panel before the coating step is preferred in some instances, e.g., to help the powder reach its flow temperature in the first zone of the oven and it also minimizes outgassing during cure.
  • the oven may have several heating zones of the IR and convection types and also a combination of the two.
  • the TRIAB Speedoven sold by Thermal Innovations Corporation is suitable for the purposes of this invention.
  • a wooden panel bearing a coating powder of this invention may be cured in a gas-fired IR oven available from Thermal Innovations Corporation by pre-heating the panel in the oven at an emitter temperature of about 1800° F. for from about 4 to about 10 seconds and post-heating at the same emitter temperature for from about 6 to about 10 seconds.
  • the surface of the panel next to the IR emitter was about 310° F. after the pre-heating and the post-heating, alike.
  • the surface opposite the IR emitter was about 50° F. as it left the oven.
  • Such relatively cool panels may be stacked atop one another as they come out of the oven. A higher emitter temperature may be used for proportionally shorter times.
  • the film thickness of the cured coating is at least about 1 mil and it may be as much as about 8 mils or even higher if there is a practical need for such. Film thicknesses of from about 4 to about 6 mils are achieved regularly by the method of this invention, even at coating line speeds of about 100 feet per minute.
  • Coating powders were made as described above from the following components:
  • Example 2 The powders of these examples were electrostatically coated on steel panels and cured at 225° F. for 10 minutes to obtain 1.8-2.2 mil thick films. As shown in Table 2, the superior solvent resistance of Examples 1 and 3 demonstrate that faster cure is achieved using this technology. Neither the conventionally extruded material (Control) nor the blend with no catalyst in Component A (Example 2) achieved full cure.
  • the coating powders of Examples 9 and 10 were deposited on pre-heated wooden panels by tribocharging guns and post-heated on a flat-line conveyor in an oven heated by IR and convection heating according to the conditions given in Table 5 wherein the results are given also.
  • the coating powder of Example 16 is the same as that of example 1 except for the addition of 0.1 part by weight of an optical brightener to both Components A and B.
  • the coating powder of Example 17 is the same as that of Example 16 except for the addition of 1.0 part by weight of IRGAFOS 168 anti-oxidant to both Components A and B of the powder of Example 16.
  • the coating powder of Example 18 is the same as that of Example 16 except for the addition of 1.0 part of IRGANOX 1425 to both Components A and B of the powder of Example 16.
  • a coating powder of Comparative Example 1 is the same as the powder of Example 16 except for the addition of 1.0 part of IRGANOX 1098 to both Components A and B of the powder of Example 16.
  • the powders of Examples 9 and 16-18, as well as the powder of the Comparative Example were deposited by a hand-operated tribocharging gun on to a surface of a 0.5 inch thick wooden panel whose temperature was about 230°-250° F. and then cured at 300°-310° F. for 30 and 60 seconds.
  • the powders of Examples 1, 9, and 10 were deposited by a hand-operated tribocharging gun on to a surface of a 0.75 inch thick wooden panel whose temperature was about 250°-270° F. and then cured at 300°-310° F. for 30, 60, and 90 seconds.
  • the SK white color shift of each cured coating is given in Table 6.
  • a cured coating having a tight, fine texture, and a slightly dry feel was obtained when a coating powder, made as described above and having a 70:30 weight ratio of Component A to Component B, was sprayed onto a horizontal panel which had been pre-heated for 5 minutes in a 350° F. oven and then heated for 10 minutes at the same temperature.
  • the cured coating had an MEK rating of 4. When the oven temperatures was 300° F., the MEK rating was the same but the coating felt less dry.

Abstract

.[.Wood.]. .Iadd.A heat sensitive substrate .Iaddend.is .[.electrostatically.]. coated with a thermosetting powder coating system in which a mixture of a self-curing epoxy resin and a catalyst therefore is extruded and .Iadd.pulverized and .Iaddend.a low temperature curing agent .[.are both.]. .Iadd.a .Iaddend.pulverized and the powders are blended with conventional additives to make a coating powder which is deposited on .[.a wooden.]. .Iadd.the .Iaddend.substrate and heated to cure. The mixture of resin and catalyst does not cure within the extruder but it is made to cure at low temperatures by the separate addition of the curing agent. A small amount of the low temperature curing agent, insufficient to cause substantial curing during extrusion may be used in place of the catalyst.

Description

This is a continuation in part of application Ser. No. 08/729,608 filed Oct. 11, 1996; which is a C-I-P of Ser. No. 08/643,694 filed on May 6, 1996 both now abandoned
BACKGROUND OF THE INVENTION
This invention relates to a two-component powder coating system by which the curing of a coating occurs at a significantly faster rate and/or at a significantly lower temperature and produces an exceptionally smooth surface. This invention also relates to thermally stable powder coating whereby white coatings do not yellow during thermal curing. This invention also relates to the electrostatic coating of metal and, in particular, to the triboelectric coating of wood with a coating powder and low temperature curing of that coating having a pleasing smoothness.
Traditionally, coating powders have been made by the extrusion of a mixture of resins and curing agents to obtain a homogeneous mixture and then grinding the extrudate and screening the comminuted product to obtain the desired particle sizes and particle size distribution. The powder is then electrostatically sprayed onto a substrate, traditionally a metal substrate, and cured at temperatures much higher than 200° F. The curing of powder coatings on heat sensitive materials such as wood, plastic, and the like has been limited by the fact that the extrusion of a mixture of a resin and a low temperature curing agent, i.e., one that is active at 200° F. or less, would cause the coating powder to gel in the extruder because the extrusion typically generates enough heat to raise the temperature to 200° F. or higher. It has been thought throughout the art that the curing agent must be mixed with the resin by extrusion to obtain a uniform cure and film appearance. It has also been commonly accepted that a low gloss film must be cured at a high temperature, e.g., about 300° F. or higher.
The powder coating of wood has been much talked about in the literature but very little has been said as to how it may be accomplished. As Douglas S. Richart said in his article published in the April, 1996 issue of POWDER COATINGS, the coating of wood with a low temperature cure powder is next to impossible because the coating must be cured at a temperature below 200° F. and the resin must have a flow temperature of about 10 to 20 degrees lower than that. Such a resin tends to block during storage at normal temperatures. Richart goes on to say that the curing agent must be sufficiently reactive that the powder will cure in a reasonable time at such low temperatures. But that leads to a possible thermosetting of the resin in the extruder. He speaks of electrostatically spraying a powder having a blocked isocyanate onto wood, heating the coating in infrared and other type ovens to form a smooth coating and curing the smooth coating with ultra-violet radiation.
In its technical bulletins, Boise Cascade shows the use of hand-held electrostatic spray guns in coating its electrically conducting particleboard.
In this invention, the epoxy resin is first extruded with a small amount of catalyst or with a low level of a low temperature curing agent and then ground and classified in the usual manner. Additional amounts of the low temperature curing agent in powder form are then blended with the powdered extrudate raise the level of curing agent while avoiding the pre-gelation problem. Surprisingly, the time required to obtain a smooth cured film is lowered significantly. It was surprising, also, that a low gloss film was achieved at cure temperatures much lower than 300° F.
SUMMARY OF THE INVENTION
It is an object of this invention, therefore, to provide a coating powder for heat sensitive substrates.
It is a related object of this invention to provide a method for coating wood without the problems associated with volatile organic solvents.
It is another object of this invention to provide a low temperature process for producing a smooth, low gloss coating on wood.
These and other objects of the invention which will become apparent from the following description are achieved by a thermosetting powder coating system in which the thermosetting of an extruded mixture of a self-curing epoxy resin and (A) a catalyst or (B) an amount of a low temperature curing agent insufficient to cause substantial curing of the resin during extrusion is facilitated by the separate addition of a low temperature curing agent; said extruded mixture and said separately added low temperature curing agent both being in powder form and being blended to form a coating powder.
DETAILED DESCRIPTION OF THE INVENTION
The curing system of this invention may be used in coating glass, ceramics, and graphite-filled composites as well as metallic substrates such as steel and aluminum but its particular utility in the coating of heat sensitive subsrates such as plastics, paper, cardboard and woods makes it highly appealing as a commercially viable alternative to the liquid coatings that have been almost universally used in the past. For the purposes of this invention, wood is defined as any lignocellulosic material whether it comes from trees or other plants and whether it be in its natural forms, shaped in a saw mill, separated into sheets and made into plywood, or chipped and made into particleboard, or its fibers have been separated, felted, and compressed. It is exemplified by lumber, panels, molding, siding, oriented strand board, hardboard, medium density fiberboard, and the like. The particle board may be standard or treated to enhance its electrical conductivity. Wood having a moisture content of from 3 to 10% by weight is suitable for the purposes of this invention. A porous particleboard, pre-coated with a conductive liquid coating composition and cured, may also serve as a substrate for the coating powder of this invention. For example, a smooth 2-3 mil thick powder coating is achieved on a 0.5 to 1 mil thick UV or thermally cured pre-coat. Without the precoat, a smooth powder coating must be about 9 mils thick.
A particularly favored embodiment of the system is one in which competing reactions are taking place simultaneously, said reactions being:
(A) a catalyzed self-curing of a portion of an epoxy resin present in an extruded mixture of the resin and a catalyst, and
(B) a crosslinking reaction between another portion of the extruded resin and a low temperature curing agent.
Epoxy resins which are useful in the practice of this invention are exemplified by, but not limited to, those produced by the reaction of epichlorohydrin and a bisphenol, e.g., bisphenol A. Preferred epoxy resins include those sold under the trademarks ARALDITE GT-7072, 7004, 3032, 6062, and 7220, and EPON 1007F, 1009F, and 1004, all of which are 4,4'-isopropylidenediphenolepichlorohydrin resins.
The epoxy resin is self-curing, i.e., it reacts via homopolymerization during curing of the powder coating. Generally, a catalyst is required to cause the reaction to progress at a commercially acceptable rate. A preferred catalyst for this invention is an epoxy adduct of an imidazole having the general formula: ##STR1## wherein R1, R2, R3, and R4 are independently hydrogen or any substituent which is not reactive with the epoxy resin. Examples of suitable imidazoles include imidazole, 2-methyl imidazole, and 2-phenyl imidazole. Suitable adducts of such imidazoles with a bisphenol A epoxy resin are available commercially from Shell Chemical Company under its trademark EPON, e.g., EPON P-101, and also from Ciba-Geigy Corporation under its designation XU HT 261. For the purposes of this invention, the term imidazole is used herein to mean both the substituted and unsubstituted imidazoles. Although applicants are not bound to any theory, it is believed that an imidazole adducts to epoxy resins by an opening of the epoxy ring that results in the epoxy oxygen bonding to the C═N bond of the imidazole ring. The adducted imidazole acts as a catalyst, moving from one epoxy group to another as it facilitates epoxy ring opening and cure reactions. Imidazoles, in themselves, tend to be insoluble in epoxy resins. Thus, the purpose for adducting them to an epoxy resin is to make them compatible with the epoxy system. As a catalyst, the imidazole adduct is used in the systems, methods, and powders of this invention at a level of from about 0.1 to about 8 parts per hundred parts of the extruded resin (phr), preferably at about 2 phr. For enhanced color stability, the 2-phenyl imidazole may be used as the catalyst for curing the epoxy resin with or without the low temperature curing agent. The 2-phenyl imidazole, which is available from the SWK Chemical Co., may be used as such at accordingly lower levels.
The imidazoles, as adducts or non-adducts, may also used at higher levels as a separately added curing agent to the extruded mixture of the resin and catalyst. When this is done, the amount of imidazole adduct is controlled so that the total amount is no more than about 12 phr.
Otherwise, the low temperature curing agent may be selected from among the many that are commercially available but an epoxy adduct of an aliphatic polyamine having a primary amino group is preferable. A suitable curing agent of that type is available from Ciba Ceigy as its PF LMB 5218 hardener. A similar product is sold under the trademark ANCAMINE 2337 XS by Air Products & Chemicals. An epoxy adduct of an aliphatic polyamine having a secondary amino group available under the trademark ANCAMINE 2014 AS is preferred for white and light colored coatings. The amount of low temperature curing agent that may be added separately as component (B) to the pulverized extrudate of resin and catalyst is from about 2 to about 40 phr and the preferred amount is from about 30 to about 35 phr. The ratio of the low temperature curing agent to the catalyst in the extrudate is from about 1:3 to about 400:1 but preferably from about 2:1 to about 15:1.
The coating powder may also contain a flow control agent in the range of from about 0.5 to about 2.0 phr. Examples of the flow control agents include the MODAFLOW poly (alkylacrylate) products and the SURFYNOL acetylenic diols; they may be used singly or in combination. Anti-oxidants may also be used at a concentration of from about 0.5 to about 2.0 phr to prevent the discoloration of the coatings even at the relatively low curing temperatures suitable for the purposes of this invention. Examples of the anti-oxidants that are useful in this invention include sodium hypophosphite, tris-(2,4-di-t-butyl phenyl) phosphite (sold under the trademark IRGAFOS 168), and calcium bis([monoethyl(3,5-di-t-butyl-4-hydroxybenzyl)phosphonate] (sold under the trademark IRGANOX 1425). Mixtures of anti-oxidants may be used.
Pigments, optical brighteners, fillers such as calcium carbonate and bentonite clays, texturizing agents such as particulate rubber, and other conventional additives may also be present. A particularly desirable textured finish may be obtained by the addition of from about 14 to about 20 phr of the rubber to the coating composition along with calcium carbonate at a rubber to carbonate ratio of from about 0.7:1 to about 1.5:1 by weight. Titanium oxide, in an amount of from about 5 to about 50 phr or more, is an example of a pigment that may be used. An optical brightener, exemplified by 2,2'-(2,5-thiophenediyl)bis[5-t-butylbenzoxazole, sold under the trademark UVITEX OB, may be present at from about 0.1 to about 0.5 phr.
For the purposes of this invention, the term resin includes the resin per se and the crosslinking agent whether it is in the extrudate or it is added separately but it does not include the catalyst.
The coating powder of this invention may be applied by any of the conventional powder coating methods but the application of the powder by triboelectric guns is preferred in particular situations such as when the wooden substrate is profiled. The grooves and ridges present a particular problem for electrostatic coating processes because of the Faraday effect. Because the electrical field generated by friction as the powder flows along the TEFLON plastic surfaces inside the gun is relatively small in comparison with the field in a corona-discharge cloud, the powder particles may be deposited more efficiently into Faraday cage areas with triboelectric guns. Wooden cabinet doors are examples of a profiled wooden substrate as are the doorskins represented by the drawings in U.S. Pat No. 5,489,460, which is incorporated herein by reference to further illustrate the type of wooden panels that are particularly susceptible to powder coating by the method of this invention. The grooves and sharp edges of such panels are covered very well on a flat line coating apparatus with nozzles arrayed to direct a portion of the powder against them.
Such panels as well as flat-surfaced panels such as those used to make ping-pong tables are particularly well coated by triboelectric guns on a flat line conveyor having electrically conductive bands around the circumference of the conveyor belt. Apparatus for such coating is disclosed in a series of patents assigned to the Nordson Corporation. These are U.S. Pat. Nos. 4,498,913; 4,590,884; 4,723,505; 4,871,380; 4,910,047: and 5,018,909; all of which are incorporated herein by reference. A suitable flat line powder coating apparatus comprises such a conveyor extending through a powder coating booth, wherein a wooden article supported and moved by the conveyor belt is coated triboelectrically by a plurality of guns situated adjacent one another and in one or more tiers. The powder is forced into the guns under about 40 psi pressure and air at about 20 psi is passed into the powder conduits just before the powder passes into the nozzles. The article bearing the powder is then conveyed through a curing oven having several heating zones, some of which are heated by IR lamps, others by heat convection, and still others by a combination of those two. The coating and curing line speeds may be the same or different depending on the the length of the curing oven. The line speed through the powder application booth may be from about 5 to about 150 feet per minute but it is preferably from about 20 to about 100 feet per minute. The line speed through the curing oven, on the other hand, may be from about 5 to about 20 feet per minute, depending on the oven temperature and the particular coating powder used. The curing temperature may range from about 180° up to but not including the decomposition temperature of the powder. It is preferred to maintain the cure temperature within the range of from about 190° to about 290° F. and still more preferred to keep the cure temperature at from about 250° to about 290° F. When a crystalline epoxy resin is used, a cure temperature of about 180° F. is particularly suitable. It is preferred that the coating and curing line speeds be adjusted to the oven length so that they are balanced.
Preheating of the panel before the coating step is preferred in some instances, e.g., to help the powder reach its flow temperature in the first zone of the oven and it also minimizes outgassing during cure. The oven may have several heating zones of the IR and convection types and also a combination of the two. The TRIAB Speedoven sold by Thermal Innovations Corporation is suitable for the purposes of this invention. A wooden panel bearing a coating powder of this invention may be cured in a gas-fired IR oven available from Thermal Innovations Corporation by pre-heating the panel in the oven at an emitter temperature of about 1800° F. for from about 4 to about 10 seconds and post-heating at the same emitter temperature for from about 6 to about 10 seconds. When a medium density fiberboard (at about 40° F.), was pre-heated and post-heated at 1800° F. for about 6 seconds and 6.5 seconds, respectively, the surface of the panel next to the IR emitter was about 310° F. after the pre-heating and the post-heating, alike. The surface opposite the IR emitter was about 50° F. as it left the oven. Such relatively cool panels may be stacked atop one another as they come out of the oven. A higher emitter temperature may be used for proportionally shorter times.
The film thickness of the cured coating is at least about 1 mil and it may be as much as about 8 mils or even higher if there is a practical need for such. Film thicknesses of from about 4 to about 6 mils are achieved regularly by the method of this invention, even at coating line speeds of about 100 feet per minute.
The invention is more specifically described in the following working examples wherein parts are by weight unless otherwise stated.
EXAMPLES 1-4 AND CONTROL
Coating powders were made as described above from the following components:
______________________________________                                    
             COMPONENTS                                                   
             (A)                                                          
             RESIN    (A)           (B)                                   
             WITH     RES-    (A**) PIG-                                  
             CATAL-   IN      CRY-  MENT  (B*)                            
             YST &    PIG-    STAL- CUR-  CAT-                            
             PIG-     MENT    LINE  ING   AL-                             
             MENT     ONLY    EPOXY AGENT YST                             
______________________________________                                    
Crystalline Epoxy RSS                                                     
             --       --      50    --    --                              
1407                                                                      
Epoxy Resin GT-7072                                                       
             100      100     50    --    --                              
Imidazole Adduct P-101                                                    
             2        --      --    --    100                             
Acrylate Flow Acid                                                        
             1.4      1.4     1.4   1.4   --                              
Benzoin      .8       .8      --    .8    --                              
Pigments     .079     .079    --    .079  --                              
TiO.sub.2 R-902                                                           
             60       60      --    60    --                              
Amine Adduct LMB-                                                         
             --       --      --    100   --                              
5218                                                                      
UVI 6974 Catalyst*                                                        
             --       --      2     --    --                              
______________________________________                                    
 *substantially nonfunctional under these conditions                      
              TABLE 1                                                     
______________________________________                                    
          Control                                                         
          1      2      3     4    Coventional Extrusion                  
______________________________________                                    
Component A                                                               
          70     --     100   --   100                                    
Component A*                                                              
          --     70     --    --   --                                     
A**       --     --     --    70   --                                     
Component B                                                               
          30     30     --    --   --                                     
Component B*                                                              
          --     --     3     --   --                                     
LMB 5218 adduct                                                           
          --     --     --    30   --                                     
______________________________________                                    
The powders of these examples were electrostatically coated on steel panels and cured at 225° F. for 10 minutes to obtain 1.8-2.2 mil thick films. As shown in Table 2, the superior solvent resistance of Examples 1 and 3 demonstrate that faster cure is achieved using this technology. Neither the conventionally extruded material (Control) nor the blend with no catalyst in Component A (Example 2) achieved full cure.
              TABLE 2                                                     
______________________________________                                    
EXAMPLE 1        2        3      4      Control                           
______________________________________                                    
MEK     Moderate Rubs     No     Moderate                                 
                                        Rubs                              
Resistance                                                                
        Rub Off  Through  Effect Rub Off                                  
                                        Through                           
(50 Double                                                                
Rubs)                                                                     
Impact  140 in-lbs                                                        
                 80 in-lbs                                                
                          60 in-lbs                                       
                                 100 in-lbs                               
                                        0 in-lbs                          
Resistance                                                                
(Direct)                                                                  
60° Gloss                                                          
        40       15       78     32     80                                
Orange Peel                                                               
        Slight   Moderate Slight Very   Slight                            
                                 Slight                                   
______________________________________                                    
                                  TABLE 3                                 
__________________________________________________________________________
Examples 5-8                                                              
            Line Preheat                          Mek Rate                
            Speed                                                         
                 Setting                                                  
                       Line Speed in                                      
                              Actual Temp.        50 Double               
                                                       Thick-             
Ex. #                                                                     
   Powder                                                                 
       Substrate                                                          
            of Coating                                                    
                 IR or Conv.                                              
                       Curing Oven                                        
                              Exiting IR                                  
                                     Appearance   Rub  ness               
__________________________________________________________________________
5  Ex. 1                                                                  
       MDF  30 ft/min                                                     
                 None  5 ft/min                                           
                              290° F.                              
                                     No outgrassing/slight                
                                                  #4llow                  
                                                       4+                 
                                     Low Gloss/Smooth                     
6  Ex. 1                                                                  
       MDF  30 ft/min                                                     
                 None  6 ft/min                                           
                              240° F.                              
                                     Slight Outgrassing/white             
                                                  #3   4+                 
                                     Higher Gloss/Slight OP               
7  Ex. 1                                                                  
       MDF  30 ft/min                                                     
                 None  5 ft/min                                           
                              260° F.                              
                                     No outgrassing/slight                
                                                  #4llow                  
                                                       4+                 
                                     Low Gloss/Smooth                     
8  Ex. 1                                                                  
       MDF  30 ft/min                                                     
                 Yes   10 ft/min                                          
                              250-280° F.                          
                                     No outgrassing/slight                
                                                  #4llow                  
                                                       4+                 
                 5 ft/mm             Low Gloss/Smooth                     
                 preheat                                                  
                 speed 180-                                               
                 200° F.                                           
__________________________________________________________________________
______________________________________                                    
                 COMPONENTS                                               
                 (A)    (B)      (C)  (D)                                 
______________________________________                                    
Epoxy Resin GT-7072                                                       
                 100    --       100  --                                  
Imidazole Adduct P-101                                                    
                 2.0    --       --   --                                  
2-Phenyl imidazole                                                        
                 --     --       2.0  --                                  
Flow Aids                                                                 
MODAFLOW 2000    1.0    1.0      1.0  1.0                                 
(SURFYNOL-104-S) 1.0    1.0      1.0  1.0                                 
TiO.sub.2 R-902  30     30       30   30                                  
Amine Adduct LMB-5218                                                     
                 --     100      --   100                                 
Polyethylene (Grade 6A)                                                   
                 2.0    2.0      2.0  2.0                                 
Sodium hypophosphite                                                      
                 1.0    1.0      1.0  1.0                                 
Optical brightener                                                        
                 0.1    0.1      0.1  0.1                                 
______________________________________                                    
              TABLE 4                                                     
______________________________________                                    
         Component Component Component                                    
                                     Component                            
EXAMPLE  A         B         C       D                                    
______________________________________                                    
9        65        35        --      --                                   
10       --        --        70      30                                   
______________________________________                                    
EXAMPLES 11-15
The coating powders of Examples 9 and 10 were deposited on pre-heated wooden panels by tribocharging guns and post-heated on a flat-line conveyor in an oven heated by IR and convection heating according to the conditions given in Table 5 wherein the results are given also.
                                  TABLE 5                                 
__________________________________________________________________________
                  Board                                                   
            Line Speed                                                    
                  Temperature                                             
                         Line Speed in                                    
                                Actual Temp.    Mek Rate 50               
Ex. #                                                                     
   Powder                                                                 
       Substrate                                                          
            of Coating                                                    
                  Before Coating                                          
                         Curing Oven                                      
                                Exiting IR                                
                                       Appearance                         
                                                Double Rub                
                                                      Thickness           
__________________________________________________________________________
11 Ex. 9                                                                  
       MDF  30 ft/min                                                     
                  290 (°F.)                                        
                         15 ft/min                                        
                                290° F.                            
                                       Good     #4    5 mils              
12 Ex. 9                                                                  
       UV-P*                                                              
            30 ft/min                                                     
                  280 (°F.)                                        
                         15 ft/min                                        
                                300° F.                            
                                       Very good                          
                                                #4-5  5 mils              
13 Ex. 9                                                                  
       UV-P*                                                              
            100 ft/min                                                    
                  290 (°F.)                                        
                         15 ft/min                                        
                                290° F.                            
                                       No pinholes                        
                                                #4-5  3+                  
14 Ex. 9                                                                  
       MDF  Hand spray                                                    
                  280° F.                                          
                          5 ft/min                                        
                                280° F.                            
                                       Very slightly yellow               
                                                --    --                  
                                       Smooth                             
15  Ex. 10                                                                
       MDF  20 ft/min                                                     
                  280° F.                                          
                          5 ft/min                                        
                                285° F.                            
                                       Whiter than Ex. 14                 
                                                --    --                  
                                       Slight Microtexture                
__________________________________________________________________________
 *UV-P stands for particleboard precoated with a UV cured liqud coating   
EXAMPLES 16-18
The coating powder of Example 16 is the same as that of example 1 except for the addition of 0.1 part by weight of an optical brightener to both Components A and B. The coating powder of Example 17 is the same as that of Example 16 except for the addition of 1.0 part by weight of IRGAFOS 168 anti-oxidant to both Components A and B of the powder of Example 16. The coating powder of Example 18 is the same as that of Example 16 except for the addition of 1.0 part of IRGANOX 1425 to both Components A and B of the powder of Example 16. A coating powder of Comparative Example 1 is the same as the powder of Example 16 except for the addition of 1.0 part of IRGANOX 1098 to both Components A and B of the powder of Example 16. The powders of Examples 9 and 16-18, as well as the powder of the Comparative Example were deposited by a hand-operated tribocharging gun on to a surface of a 0.5 inch thick wooden panel whose temperature was about 230°-250° F. and then cured at 300°-310° F. for 30 and 60 seconds. The powders of Examples 1, 9, and 10 were deposited by a hand-operated tribocharging gun on to a surface of a 0.75 inch thick wooden panel whose temperature was about 250°-270° F. and then cured at 300°-310° F. for 30, 60, and 90 seconds. The SK white color shift of each cured coating, as measured with a MacBeth 2020+ spectrophotometer using the CIELAB COLORSPACE Delta B-(+) yellowness scale, is given in Table 6.
              TABLE 6                                                     
______________________________________                                    
         Panel  Delts B*+                                                 
EXAMPLE    Thickness                                                      
                    30 secs.  60 secs.                                    
                                    90 secs.                              
______________________________________                                    
 9          0.5 in. 1.7       2.0   --                                    
16         "        3.9       7.9   --                                    
17         "        2.1       3.0   --                                    
18         "        3.4       6.0   --                                    
Comp. Ex.  "        7.7       13.5  --                                    
 1         0.75     4.7       9.1   9.5                                   
 9         "        2.5       4.2   4.5                                   
10         "        1.5       2.7   2.8                                   
______________________________________                                    
                     (A)    (B)                                           
______________________________________                                    
Epoxy Resin GT-7072  100    --                                            
Imidazole Adduct P-101                                                    
                     2.0    --                                            
Flow Aid             1.0    1.0                                           
Carbon black         3.0    3.0                                           
Amine adduct LMB-5218                                                     
                     --     100                                           
Polyethyene (Grade 6A)                                                    
                     2.0    2.0                                           
Calcium carbonage    15.0   15.0                                          
Nitrile rubber       17.0   17.0                                          
(NIPOL 1422)                                                              
______________________________________                                    
A cured coating having a tight, fine texture, and a slightly dry feel was obtained when a coating powder, made as described above and having a 70:30 weight ratio of Component A to Component B, was sprayed onto a horizontal panel which had been pre-heated for 5 minutes in a 350° F. oven and then heated for 10 minutes at the same temperature. The cured coating had an MEK rating of 4. When the oven temperatures was 300° F., the MEK rating was the same but the coating felt less dry.

Claims (6)

The subject matter claimed is:
1. A method for coating wood comprising electrostatically spraying a coating powder selected from the group consisting of
(A) a blend comprising (i) a powdered, extruded mixture of a self-curing epoxy resin and a catalyst therefore, and (ii) a powdered, low temperature curing agent; and
(B) a blend comprising (i) a powdered, extruded mixture of a self-curing epoxy resin and an amount of a low temperature curing agent insufficient to cause substantial curing of the resin during extrusion, and (ii) a sufficient amount of the same or different low temperature curing agent in powder form to complete the curing of the resin onto a surface of the wood to a thickness of from about 3 to about 6 mils, and curing the powder at a temperature of from about 180° F. up to but not including the decomposition temperature of the blend.
2. The method of claim 1 wherein the low temperature curing agent is an epoxy resin adduct of an aliphatic polyamine having a primary amino group.
3. The method of claim 1 wherein the catalyst is an epoxy adduct of an imidazole having the general formula: ##STR2## wherein R1, R2, R3, and R4 are independently hydrogen or any substituent which is not reactive with the epoxy resin.
4. The method of claim 1 wherein the electrostatic spraying is triboelectric. .Iadd.
5. A method for coating a heat sensitive substrate comprising applying a coating powder selected from the group consisting of
(A) a blend comprising
(i) a powdered, extruded mixture of an epoxy resin and a catalyst therefore, and (ii) a powdered, low temperature curing agent; and
(B) a blend comprising
(i) a powdered, extruded mixture of an epoxy resin and an amount of a low temperature curing agent insufficient to cause substantial curing of the resin during extrusion, and (ii) a sufficient amount of the same or different low temperature curing agent in powder form to complete the curing of the resin
onto a surface of the substrate to a thickness of at least about 1 mil, and curing the powder at a temperature of from about 180° F. up to but not including the decomposition temperature of the blend..Iaddend..Iadd.
6. The method of claim 5 wherein the low temperature curing agent is an epoxy resin adduct of an alipbatic polyamine having a primary or secondary amino group..Iaddend..Iadd.7. The method of claim 5 wherein the powder is electrostatically sprayed onto the surface..Iaddend..Iadd.8. The method of claim 5 wherein the catalyst is an imidazole having the general formula: ##STR3## wherein R1, R2, R3, R4 are independently hydrogen or any substituent which is not reactive with the epoxy resin..Iaddend..Iadd.9. The method of claim 2 wherein the catalyst is an epoxy adduct of an imidazole having the general formula: ##STR4## wherein R1, R2, R3, R4 are independently hydrogen or any substituent which is not reactive with the epoxy resin..Iaddend..Iadd.10. The method of claim 2 wherein the catalyst is an imidazole having the general formula: ##STR5## wherein R1, R2, R3, R4 are independently hydrogen or any substituent which is not reactive with the epoxy resin..Iaddend.
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US08/917,043 Expired - Lifetime US6077610A (en) 1996-05-06 1997-08-19 Two component powder coating system and method for coating wood therewith
US08/914,490 Expired - Lifetime US5907020A (en) 1996-05-06 1997-08-19 Two component powder coating system and method for coating wood therewith
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US08/917,043 Expired - Lifetime US6077610A (en) 1996-05-06 1997-08-19 Two component powder coating system and method for coating wood therewith
US08/914,490 Expired - Lifetime US5907020A (en) 1996-05-06 1997-08-19 Two component powder coating system and method for coating wood therewith

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8187702B1 (en) 2011-01-21 2012-05-29 The Diller Corporation Decorative laminate and method of making
US8496762B2 (en) 2011-02-04 2013-07-30 Roberto Zoboli Aluminum treatment compositions

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2166450C (en) * 1995-01-20 2008-03-25 Ronald Salovey Chemically crosslinked ultrahigh molecular weight polyethylene for artificial human joints
EP0877769B1 (en) * 1996-02-02 2002-05-02 Vantico AG Process for coating a heat-sensitive substrate by using a storage-stable moulding powder based on epoxy resins
JP4005184B2 (en) * 1997-09-01 2007-11-07 インターメタリックス株式会社 Powder coating and film formation method using the powder coating
EP0916709B2 (en) * 1997-11-04 2010-02-17 Morton International, Inc. A one-component, low temperature curable coating powder
US6890999B2 (en) * 1997-11-04 2005-05-10 Rohm And Haas Company Coating powder of epoxy resin and low temperature curing agent
US6703070B1 (en) * 1997-11-04 2004-03-09 Morton International, Inc. One-component, low temperature curable coating powder
US6153267A (en) * 1999-03-10 2000-11-28 Morton International Inc. Method of applying a coating powder to a substrate
WO2001018130A1 (en) * 1999-09-02 2001-03-15 Gmbh Clariant Method for brightening workpieces by powder coating
US6238750B1 (en) 1999-10-12 2001-05-29 Rohm And Haas Company Powder coating involving compression of the coating during curing
US6294610B1 (en) 1999-11-29 2001-09-25 Rohm And Haas Company Coating powders for heat-sensitive substrates
US6479585B2 (en) 2000-05-26 2002-11-12 H. B. Fuller Licensing & Financing Inc. Power coating of carboxyl-functional acrylic resin and polyepoxy resin
US6541544B1 (en) 2000-05-26 2003-04-01 H. B. Fuller Licensing & Financing, Inc. Textured weatherable powder coatings
US6601357B2 (en) 2000-09-06 2003-08-05 George Tunis Un-reinforced thermoplastic coating
US6537671B2 (en) 2000-12-05 2003-03-25 Alpha Coating Technologies, Llc Coating powders having enhanced electrostatic chargeability
US7223477B2 (en) * 2000-12-05 2007-05-29 Alpha Coating Technologies, Llc Coating powders having enhanced flexability
US6627131B2 (en) * 2001-02-09 2003-09-30 Georgia-Pacific Resins, Inc. Method for introducing an additive to a composite panel
US7091286B2 (en) * 2002-05-31 2006-08-15 Ppg Industries Ohio, Inc. Low-cure powder coatings and methods for using the same
US6737163B2 (en) * 2002-05-31 2004-05-18 Ppg Industries Ohio, Inc. Low-cure powder coatings and methods for using the same
US6964722B2 (en) * 2002-08-07 2005-11-15 Trio Industries Holdings, L.L.C. Method for producing a wood substrate having an image on at least one surface
US6998365B2 (en) * 2003-09-29 2006-02-14 Ppg Industries Ohio, Inc. Catalysts for low-cure powder coatings and methods for using the same
US20090004496A1 (en) * 2004-07-27 2009-01-01 Orica Australia Pty Ltd System for Providing Powder Coated Reconstituted Cellulosic Substrate
GB0423349D0 (en) * 2004-10-21 2004-11-24 Hexcel Composites Ltd Fibre reinforced assembly
US7637558B2 (en) * 2004-11-12 2009-12-29 Société en Commandite Prolam System and method for providing reinforcement and/or moisture protection at discrete locations on a wooden cargo-carrying floor
US8026310B2 (en) * 2005-03-10 2011-09-27 Alpha Coating Technologies, Inc Coating powder of epoxy resin, styrene-maleimide curing agent and a second curing agent
US20060204759A1 (en) * 2005-03-10 2006-09-14 Jeno Muthiah Low temperature curing coating powder
GB2428395B (en) * 2005-07-19 2007-09-05 Ian Webb A process of powder coating and a powder coating apparatus
US20070193179A1 (en) * 2006-01-27 2007-08-23 Prolam, Societe En Commandite Wooden laminated floor product to improve strength, water protection and fatigue resistance
CA2605215C (en) * 2006-10-02 2014-12-02 Prolam, Societe En Commandite Utilization of coloration to improve the detection of "hit or miss" defects when using scanner equipment and an automated saw to remove defects in wood pieces
US20120151872A1 (en) * 2007-10-09 2012-06-21 Stormwall Systems Llc Wall panel and method of fabrication and use
EP2342286B1 (en) * 2008-11-07 2014-06-25 DSM IP Assets B.V. Heat-curable powder coating composition
JP2012508279A (en) 2008-11-07 2012-04-05 ディーエスエム アイピー アセッツ ビー.ブイ. Thermosetting powder coating composition
US20140364540A1 (en) 2009-02-26 2014-12-11 Jotun Powder Coatings (N) As Powder coating
AU2011249732B2 (en) 2010-05-06 2013-12-12 Covestro (Netherlands) B.V. Low temperature heat-curable powder coating composition comprising a crystalline polyester resin, an amorphous resin and a peroxide
PL2566923T3 (en) 2010-05-06 2017-07-31 Dsm Ip Assets B.V. Low temperature cure heat-curable powder coating composition comprising a crystalline polyester resin, an amorphous polyester resin, a crosslinking agent and a thermal radical initiator
EP2450109A1 (en) * 2010-11-09 2012-05-09 Grumble & Marker Industries, Inc. Powder coating
CN102353471B (en) * 2011-07-06 2013-05-22 西安交通大学 Linear temperature sensor and manufacturing method thereof
FR2987762A1 (en) * 2012-03-08 2013-09-13 Epi Nouvelles Technologies Epi Nt Method for applying e.g. decorative powder on metal part, involves preceding electrostatic pulverization of painting powders by step of pre-heating of metal parts to be painted such that parts are presented at predetermined temperature
US8721396B1 (en) * 2013-03-12 2014-05-13 BTD Wood Powder Coating, Inc. Method for preparing and buffing a powder coated wood substrate
US9358580B1 (en) 2013-03-12 2016-06-07 BTD Wood Powder Coating, Inc. Method for preparing and top coating a powder coated wood substrate
CA2909325C (en) 2013-04-26 2021-01-26 Dsm Ip Assets B.V. Vinyl functionalized urethane resins for powder coating compositions
ES2661250T3 (en) 2013-11-21 2018-03-28 Dsm Ip Assets B.V. Thermosetting powder coating compositions comprising methyl substituted benzoyl peroxide
US9630197B1 (en) 2016-03-08 2017-04-25 Troy Greenberg Dynamic powder dispersing system
JP6521918B2 (en) * 2016-08-24 2019-05-29 トヨタ自動車株式会社 Heat sink manufacturing method
CN112094567A (en) * 2020-08-25 2020-12-18 上海汉中涂料有限公司 Waterborne epoxy high-gloss terrace varnish
CN113621264A (en) * 2021-06-23 2021-11-09 天津西敦粉漆科技有限公司 Method for preparing low-temperature curing powder coating in post-mixing mode, related composite nano low-temperature curing catalyst and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3384610A (en) * 1964-05-25 1968-05-21 Dexter Corp Fluidized bed coatings containing powdered epoxy resin compositions and method for preparing the same
DE2418754A1 (en) * 1973-04-18 1974-11-07 Morton Norwich Products Inc Latent hardener for epoxy resins - contg. aromatic acid anhydride and imidazole cpd
US5212263A (en) * 1991-01-10 1993-05-18 Morton International, Inc. Textured epoxy powder coating

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB963557A (en) * 1962-10-11 1964-07-08 Shell Int Research Epoxy resin composition
IT944499B (en) * 1971-01-18 1973-04-20 Beatrice Foods Co ELECTROSTATIC METHOD FOR THE APPLICATION OF A MULTI-LAYER COATING AND PRODUCT THUS OBTAINED
BE789216A (en) * 1971-10-01 1973-03-26 Shell Int Research OMPOSITIES WERKWIJZE TER BEREIDING VAN POEDERVORMIGE DEKLAAGC
US4009301A (en) * 1974-09-05 1977-02-22 Owens-Illinois, Inc. Method for powder coating
DE3815288A1 (en) * 1988-05-05 1989-11-16 Kurt Weigel Process for the preparation of powder coatings having unusual properties
CA1326096C (en) * 1988-08-19 1994-01-11 Katugi Kitagawa Epoxy resin powder coating composition with excellent adhesibility
IT1243350B (en) * 1990-07-18 1994-06-10 Hoechst Italia PROCEDURE FOR THE COATING OF HEAT-SENSITIVE MATERIALS WITH POWDER PAINT
US5344672A (en) * 1992-05-14 1994-09-06 Sanderson Plumbing Products, Inc. Process for producing powder coated plastic product
US5407978A (en) * 1993-05-07 1995-04-18 Minnesota Mining And Manufacturing Company Rapid curing powder epoxy coating compositions having increased flexibility, incorporating minor amounts of aliphatic triepoxides
SE504784C2 (en) * 1995-08-10 1997-04-21 Herberts Powder Coatings Ab Process for powder coating and powder for carrying out the process
EP0877769B1 (en) * 1996-02-02 2002-05-02 Vantico AG Process for coating a heat-sensitive substrate by using a storage-stable moulding powder based on epoxy resins
US5686185A (en) * 1996-06-28 1997-11-11 Morton International, Inc. Disbondment resistant epoxy powder coating composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3384610A (en) * 1964-05-25 1968-05-21 Dexter Corp Fluidized bed coatings containing powdered epoxy resin compositions and method for preparing the same
DE2418754A1 (en) * 1973-04-18 1974-11-07 Morton Norwich Products Inc Latent hardener for epoxy resins - contg. aromatic acid anhydride and imidazole cpd
US5212263A (en) * 1991-01-10 1993-05-18 Morton International, Inc. Textured epoxy powder coating

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8187702B1 (en) 2011-01-21 2012-05-29 The Diller Corporation Decorative laminate and method of making
US8496762B2 (en) 2011-02-04 2013-07-30 Roberto Zoboli Aluminum treatment compositions

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EP0942050B1 (en) 2006-01-18
ES2205125T3 (en) 2004-05-01
CA2202336C (en) 2000-07-18
DE69735142D1 (en) 2006-04-06
EP0806445B1 (en) 2003-08-13
EP0806445A2 (en) 1997-11-12
DE69724032D1 (en) 2003-09-18
MX9703117A (en) 1998-12-31
US5907020A (en) 1999-05-25
US6077610A (en) 2000-06-20
EP1424142A1 (en) 2004-06-02
DE69724032T2 (en) 2004-02-19
CA2202336A1 (en) 1997-11-06
EP0806445B2 (en) 2010-11-17
ES2257007T3 (en) 2006-07-16
US5714206A (en) 1998-02-03
EP0806445A3 (en) 1998-07-22
DE69724032T3 (en) 2011-06-09
EP0942050A2 (en) 1999-09-15
DE69735142T2 (en) 2006-10-26
ES2205125T5 (en) 2011-04-08

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