Classifications

• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
  • C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
• • 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
  • B05D3/04—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 gases
  • B05D3/0493—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 gases using vacuum
• • 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
  • B05D7/06—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 to wood
  • B05D7/08—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 to wood using synthetic lacquers or varnishes
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
  • B05D7/50—Multilayers
  • B05D7/52—Two layers
  • B05D7/54—No clear coat specified
  • B05D7/544—No clear coat specified the first layer is let to dry at least partially before applying the second layer
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
  • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
  • C04B41/52—Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
  • C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
  • C04B41/61—Coating or impregnation
  • C04B41/70—Coating or impregnation for obtaining at least two superposed coatings having different compositions
• • 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
  • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
  • C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation

Definitions

• This invention relates to a method of applying a powder coating to a non-metallic substrate, such as for example cement bound particle board
• Powder coating is the term given to the application of a decorative coating principally to metallic articles
• the coating is applied to the article in an electrostatic field by propelling dry pigmented particles from a special gun, which is friction or electrostatically activated, towards the article the particles being attracted to the article by electrostatic forces
• the particles adhere to the surface of the article, and depending upon the force of the electrostatic field, successive particles adhere until the required build up is achieved whereafter any surplus powder falls from the article and may be recovered
• the article is then moved through a suitable oven at elevated temperatures usually in the range of 140°C, to 185°C, or at lower temperatures in the presence of ultra violet light, to cause the powder particles to melt, flow, coalesce and cure to form a coating
• powder coating are very tough and resistant to wear and in exterior grades resistant to weathering
• the powder coating method is solventless and because the powder can be recovered for reuse, wastage is virtually nil
• the thickness of the coating on the article may be very accurately controlled
• the method is of particular application to articles of complex shape Powder coatings are further characterised by their flexibility and adhesion so that, after powder coating, an article such as a flat sheet may be post formed over curves or edges
• One powder coating technique requires that the article to be coated must be able to sustain an electrostatic field for the particles of the powder coating composition to adhere thereto It is possible that an article which does not retain an electrostatic field could be dampened or wetted in order for the particles of the powder coating composition to adhere to the article However oven heating of the article may lead to the commencement of decomposition or to "blowing' as gasses escape through the coalescing powder film from the heated article
• fusion coating wherein the article is preheated before applying the powder coating, such as in a fluidized bed
• PCT Patent Application No PCT/GB 97/01464 (WO 97/45591 ) to Windsor Technologies Limited teaches a method of applying a powder coating to a length of a lignoceliulosic material
• the method includes the steps of impregnating the material with an impregnating composition comprising either a dicarboxylic anhydride or a t ⁇ carboxylic anhydride dissolved in a suitable non-aqueous solvent or an isocyanate thermosetting resin dissolved in a suitable non-aqueous solvent or a combination of the two, if necessary removing from the impregnated length of material any excess of the impregnating composition removing the non-aqueous solvent or solvents, placing the impregnated length of lignoceliulosic material in an electrostatic field or in a fluidised bed and applying a powder coating composition thereto so that the powder coating composition adheres thereto and then subjecting the length of lignoceliulosic material to elevated temperatures to poly
• UK Patent No 1 ,348,272 teaches the powder coating of a length of paper while still damp with abrasion resistant particles, such as quartz or corundum, in which the electrostatic attraction is achieved by the presence of water This however necessitates the drying of the material before the curing of the either pre- or post- applied thermosetting resin
• the binder composition comprises a polymer having a degree of unsaturation between 300 and 1800 grams per mole of unsaturated group (WPU), having a molecular weight n between 800 and 6800 and a viscosity between 1 dPas and 800 dPas, and a cross-linking agent having vinyl ether, vinyl ester or (meth)acrylate functional groups
• WPU grams per mole of unsaturated group
• the polymer is preferably an unsaturated polyester and/or an unsaturated polyacrylate
• the binder composition can be used in the preparation of powder paint formulations which can be applied to heat-sensitive substrates such as wood and plastic and which can be cured with UV or electron beam radiation
• composition containing a polyester resin which is selected from (i) a pre-accelerated, unsaturated polyester resm containing a latent catalyst therefor, dissolved in a suitable non-aqueous solvent, and
• step (c) placing the substrate from step (b) in an electrostatic field or in a fluidised bed and applying a powder coating composition to the substrate so that the powder coating composition adheres to the substrate, and
• step (d) then subjecting the substrate of step (c) to an elevated temperature to polymerise and/or cross-link the polyester resm in or on the substrate and to cure the powder coating composition to form the powder coating
• the non-metallic substrate may be for example a length of a lignoceliulosic material, e g a length of paper or cardboard or wood, a length of a fibre board such as medium density fibre board, high density fibre board, or a fibre reinforced phenolic composite, a cementitious product such as a fibre cement or cement bound particle board, or a cement expanded mineral composite product, or the like
• the method of the invention may include various optional steps
• step (e) after step (b) and before step (c) pre-heating the substrate or
• step (f) after step (b) and before step (c) subjecting the substrate to a vacuum or
• step (g) after step (b) and before step (c) pre-heating the substrate and then subjecting the substrate to a vacuum
• the composition may include a dicarboxylic anhydride or a t ⁇ carboxylic anhydride dissolved in a suitable solvent such as a non-aqueous solvent which may be the same as or compatible with the non-aqueous solvent for the polyester resm, or such as water
• the composition may also include a styrene polymer dissolved in a suitable non-aqueous solvent which may be the same as or compatible with a non- aqueous solvent for the polyester resm DESCRIPTION OF EMBODIMENTS
• the crux of the invention is that a non-metallic substrate is either impregnated or surface coated with a polyester resm and in this way is modified so that it induces an electrostatic attraction that the surface of the substrate is stabilised, hardened and strengthened, that the polyester resm in the treated substrate forms a chemical linkage to the applied powder coating, and that the chemical reactions involved do not emit a gas, which all contribute to the successful powder coating of the substrate
• Step (a) of the method of the invention is to impregnate the substrate or to apply to the surface of the substrate a composition comprising a pre-accelerated polyester resin containing a latent catalyst therefor either dissolved in a suitable non-aqueous solvent or mixed or dispersed in water
• the polyester resin may be any suitable unsaturated polyester resm
• An example of a suitable resin is an isophtha c neopentyl glycol unsaturated polyester resm, developed for applications where good chemical and water resistance are essential
• a specific example is NCS Ultraset 993 by NCS Resins of South Africa which is especially designed for filament winding, marine swimming pools and PVC laminate applications This resm has the following properties
• a rigid polyester resin such as NCS 33410 which is a rigid isophthalic resm with an adipic acid modified unsaturated polyester resin, particularly the isophthalics such as 8130 by NCS Resins of South Africa, added in an amount of up 50% by weight of the rigid polyester resin, so as to render the resin more flexible
• the properties of cured 8130 are
• the unsaturated polyester resin must be pre-accelerated
• the resm is pre-accelerated typically with a cobalt naphthanate or a cobalt octoate in white spirits, in an amount of from 0,25% to 1 ,5% inclusive by weight on the weight of the resin
• the resin is thereafter catalysed with a latent catalyst which will decompose and trigger polymerisation at temperatures in the region of 60°C upwards, more typically above 80°C
• suitable latent catalysts are a di-tertiary-butyl peroxy 3,3,5-tr ⁇ - methyl cyclohexane in t ⁇ -butyl phthalate such as T ⁇ ganox 29B 240 or T ⁇ ganox 29B 50 by Akzo Chemie and benzoyl peroxide formulations such as tert-butyl perbenzoate, sold by Interox under the codes TBTB and others
• the unsaturated polyester resin may be dissolved in a suitable non-aqueous solvent
• a suitable non-aqueous solvent The choice of solvent is dictated by cost toxicity evaporative rate and compatibility with the other components of the composition
• suitable non-aqueous solvents are dichloromethane and acetone
• the unsaturated polyester resin may be one which is dispersible or miscible in water, in which case water may oe used as the carrier
• the composition preferably contains the polyester resin in an amount of from 15% to 40% inclusive of the polyester resin by weight of the composition
• the remainder of the composition is made up of the non-aqueous solvent or water, optionally an additional component such as an anhydride or a styrene polymer as is discussed in more detail below, the pre-accelerator, and the catalyst
• the catalyst is preferably present in an amount of from 0 2% to 0,8% by weight of the composition
• composition may also include a dicarboxylic anhydride selected from the group consisting of maleic anhydride, phthalic anhydride succmic anhydride and tetrahydrophthahc anhydride or a t ⁇ carboxylic anhydride such as t ⁇ mellitic anhydride
• a dicarboxylic anhydride selected from the group consisting of maleic anhydride, phthalic anhydride succmic anhydride and tetrahydrophthahc anhydride or a t ⁇ carboxylic anhydride such as t ⁇ mellitic anhydride
• anhydride is maleic anhydride
• the anhydride is dissolved in a suitable solvent which must be compatible with the solvent for the resin, or water
• a suitable solvent which must be compatible with the solvent for the resin, or water
• the anhydride is dissolved in the same solvent as the resm, for example dichloromethane or acetone
• the purpose of the anhydride is to maximise the electrostatic attraction of the treated non-metallic substrate It is also chosen for compatibility with the polyester resm
• the preferred anhydride is maleic anhydride which has a di-elect ⁇ c loss factor of 0,97 in dichloromethane
• the anhydride is preferably present in an amount of from 1 % to 6%, more preferably from 1 to 4%, by weight of the composition
• the composition may also include a styrene polymer, e g a styrene homopolymer, copolymer or terpolymer
• the styrene polymer may be a homopolymer, e g polystyrene, or a copolymer such as styrene acrylonit ⁇ le or styrene polybutadiene, or a terpolymer such as acrylonitnle polybutadiene styrene or a blend between them
• styrene polymer imposes resistance to water uptake and to water ingress on the treated material minimises dimensional change, particularly shrinkage on drying, improves hardness
• styrene polymers have high resistance to chemicals
• the homopolymer polystyrene itself is very hard Polystyrene has a specific gravity of 1 ,05 to 1 ,07 and a percentage water absorption after 24 hours of immersion of between 0,04 and 0,06%
• the copolymerisation of styrene with another monomer imposes special properties such as toughness
• the styrene polymer may be dissolved in any suitable non-aqueous solvent which may be the same as, or compatible with, the solvent used for the polyester resin
• the styrene polymer may be dissolved in dichloromethane or acetone, or may be dissolved in toluene to render it compatible with the polyester resin composition
• the styrene polymer is preferably present in an amount of from 1 % to 5% by weight of the composition
• the substrate may be impregnated with the composition in any suitable manner Examples of methods of impregnation are to be found in PCT/GB 97/00440 (WO 97/32074) and PCT/GB 97/01464 (WO 97/44591 ) both of which are incorporated herein by reference
• the impregnation may be carried out by irrigating the substrate with the composition or by immersing the substrate in the composition
• the substrate may simply be surface coated with the composition, again in any suitable manner, such as for example by spraying
• step (a) if necessary there may be removed from the impregnated or coated substrate any excess of the composition
• step (b) the non-aqueous solvent or the water is removed This may be achieved using electronically induced heat such as infrared induced heat, or any other suitable method When the solvent is a non-aqueous solvent it may be recaptured for reuse
• the treated substrate may be pre-heated or may be subjected to a vacuum or may be pre-heated and then subjected to a vacuum, the purpose being to de-gas and de-humidify the substrate to minimise gassing during the powder coating step
• step (c) of the method of the invention the substrate is placed in an electrostatic field or in a fluidised bed and a powder coating composition is applied thereto
• the powder coating composition in the form of a finely divided pre- formulated dry powder, is propelled towards the surface of the substrate from a suitably charged applicator gun, either friction or electrostatic, such that the particles of the powder coating composition adhere to the surface of the substrate
• Electrostatic charged guns are preferred such as the Super Carona by Gema Any particles of the powder coating composition that do not adhere to the surface of the substrate, fall from the substrate and may be recovered
• suitable powders are polyurethanes or epoxy polyesters for interior use or pure polyesters for exterior use, in gloss, suede or matte, in textures, hammer tones, metallics, pearlescents, wrinkle finishes or multi colours
• Curing temperatures are from as low as 100°C in the presence of ultra violet light using photosensitive catalysis, or in the range of 140°C -185°C with a cure time of 5 to 15 minutes
• step (d) of the method of the invention the substrate is subjected to an elevated temperature to polymerise and/or cross-link the polyester resin in or on the substrate and to cure the powder coating composition to form the powder coating
• the length of the substrate may be passed through a space heater in which the temperature of the substrate is raised to a level above 140 C C, more usually up to 185°C
• a preferred form of heating is surface heating using infrared
• a typical formulation of a composition for impregnation or surface coating of a substrate is as follows Acetone 350
• a substrate such as a length of medium density fibre board is impregnated with the above composition and any excess of the composition is then removed
• the treated substrate is powder coated with a suitable powder coating composition and the polyester resm and powder coating are then set and cured
• the result is a length of medium density fibre board with a decorative powder coating, which may be used for the formation of wall units or cupboards or the like

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• 2000
  • 2000-10-20 CA CA002388420A patent/CA2388420A1/en not_active Abandoned
  • 2000-10-20 JP JP2001533913A patent/JP2003512922A/ja active Pending
  • 2000-10-20 AU AU78114/00A patent/AU769055B2/en not_active Ceased
  • 2000-10-20 CN CN00814810A patent/CN1382074A/zh active Pending
  • 2000-10-20 WO PCT/IB2000/001510 patent/WO2001030927A2/en not_active Application Discontinuation
  • 2000-10-20 EP EP00968163A patent/EP1230039A2/de not_active Withdrawn

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