US2601284A - Heat resistant panel - Google Patents

Heat resistant panel Download PDF

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Publication number
US2601284A
US2601284A US722840A US72284047A US2601284A US 2601284 A US2601284 A US 2601284A US 722840 A US722840 A US 722840A US 72284047 A US72284047 A US 72284047A US 2601284 A US2601284 A US 2601284A
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Prior art keywords
veneer
coating
approximately
resin
adhesive
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US722840A
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Charles B Hemming
Ray L Overholt
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United States Plywood Corp
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United States Plywood Corp
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    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04FFINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
    • E04F13/00Coverings or linings, e.g. for walls or ceilings
    • E04F13/07Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor
    • E04F13/08Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor composed of a plurality of similar covering or lining elements
    • E04F13/10Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor composed of a plurality of similar covering or lining elements of wood or with an outer layer of wood
    • 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]
    • Y10T428/31678Of metal
    • Y10T428/31688Next to aldehyde or ketone condensation product
    • 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]
    • Y10T428/31678Of metal
    • Y10T428/31692Next to addition polymer from unsaturated monomers
    • 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]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/3188Next to cellulosic
    • Y10T428/31895Paper or wood
    • Y10T428/31899Addition polymer of hydrocarbon[s] only
    • 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]
    • Y10T428/31942Of aldehyde or ketone condensation product
    • Y10T428/31949Next to cellulosic
    • Y10T428/31957Wood

Definitions

  • This invention relates to the woodworking eld, and particularly to the building material industry, the furniture industry, and the fancy container industry.
  • One of the objects of this invention is to provide a cigarette-proof, scorchproof, or burnproof material which will withstand the heat of cigarettes indelinitely, and, also, for a short period time, will withstand the heat of hot pans, hot irons, and other hot objects, without marring the nish or the veneer proper.
  • Another object of this invention is to provide a surface coating which will form a high finish on the veneer and make the veneer appear extremely brilliant and glossy, while at the same time the coating itself acts as a protective shield for the wood against marring by heat and water.
  • Still another object of the invention is to impart a finish to a wood veneer which by combination of a high refractive index and good wetting action, i. e., excellent, intimate contact between the iilm and the veneer with resultant displacement of air, brings out the contrast and texture in startling fashion but without staining or changing the color or tone of the veneer in any way.
  • a fourth object of this invention is to mask the grain and checks in the relatively inexpensive base material, such as, fir, by providing a layer of metal or inexpensive hardwood between the base material and the expensive face veneer.
  • a fth object of this invention is to provide on a panel a surface coating having a brilliant nish produced by heating certain resins and catalysts at low temperatures for a short period of time.
  • Cigarette-proof panels have been made in the past by taking a stack of thin paper sheets or rags, completely impregnating the stack with a resin, and subsequently subjecting the stack to a high pressure under heat. Large quantities of resin are expensive, and the initial cost and maintenance cost of high pressure presses, and solid, sturdy foundations and buildings to house such high pressure presses, are also expensive. In addition, the resulting product is not particularly attractive to most people because it looks artificial and lacks life. cult to produce at panels. This is the rst time, as far as is known, that a cigarette-proof or heat-proof board having a brilliant finish which sets off the grain has been made by the low pressure and, hence, inexpensive method.
  • Fig. 1 is a cross-sectional view of one embodiment of our invention showing not only the brilliant finish but also the metallic heat dispersing element.
  • Fig. 2 is a modified form of our invention illusstrating a different type base material, and having a brilliant surface coating applied to both sides of the panel.
  • Fig. 3 is a further modication and discloses a different base material and a metal heat conducting material between the base and the face veneer.
  • Fig. Ll is a still further modication of 'our invention and shows a lumber base material and a relatively inexpensive hardwood veneer between the base material and the expensive face veneer.
  • a plywood panel is indicated by numeral 4 and comprises veneers I, 2 and 3.
  • This base material is preferably iir plywood or pine plywood or some other of the inexpensive coniferous species.
  • the basic material has been illustrated as plywood. However, even though plywood performs much better than other materials due to its great strength per unit weight, it is understood that other base materials, such as illustrated in Figs. 2, 3 or 4, may be used.
  • thermosetting resin such as, phenol formaldehyde, urea formaldehyde, melamine aldehyde, furfural resin., polyvinyl resin, or any of the synthetic rubber cements, or a mixture of phenol formaldehyde resin and butadiene acrylonitrile synthetic rubber, or a mixture of synthetic rubber derivative mixed with phenol formaldehyde resin, or other adhesive which will bind metal to wood, may be applied.
  • thermosetting resins take a comparatively long time to set and are not suffrciently elastic or flexible after setting. Thermoplastic resins, on the other hand, are too elastic when set.
  • An aluminum sheet or aluminum foil, a copper sheet or copper foil, a copper clad iron plate., or some other appropriate metal element 6 is placed over the adhesive and a second layer of adhesive is applied to the metallic element. Since the wood base will absorb moisture from the adhesive, in most cases it will be found advantageous to apply bothcoats of adhesive to the metal foil.
  • both sides may be coated by one passing through the roller coating or glue spreading machine.
  • the adhesive should then be partially or fullydried before assembling the veneer to the metal element.
  • Adhesive may also be applied by spraying, dipping, or other conventional ways of coating.
  • a veneer preferably an expensive veneer, such as, teak, mahogany, etc., of the order of 1/24 inch to 175 inch, is placed.
  • a heat and water resistant protective coating c of a polyester resin, such as, styrene alkyd and a catalyst is applied.
  • the coating may be applied by spraying, dipping or otherwise coating the outer surface of the thin veneer.
  • the resin in order to obtain an exceptionally brilliant finish, the resin must be entirely free of all dirt or dust.
  • Favorableresults may be obtained in an Vair conditioned room, but the following procedure has been found to be the best method of applying the resin to the veneer.
  • a temporary metallic transfer plate (not shown in the drawing), preferably a chromium plated metal of some kind, such as, iron, steel, stainless steel, etc., having a smooth finish' and high polish, is rubbed liberally with a parting agent, such as, a fatty component of certain vegetable oils, such as, soy bean and castor, generally known as lethicin, carnauba wax, silicone grease, etc., and subsequently is covered with the resin coating.
  • the temporary transfer plateA is then heated so that the resin will become firm or gelled in its intermediate stage.
  • the time for the resin to gell is short, i. e., thirty minutes or less, and the temperature comparatively low, i. e., approximately 150 F.
  • styrene alkyd with a benzoyl peroxide lcatalyst will set in twenty minutes at 150 F. temperature
  • styrene alkyd with a tertiary butyl hydroperoxide catalyst will set in ten minutes Aat 150 F. temperature.
  • the rapidity with which the resin becomes firm is exceedingly important because the output of the plant is directly proportional to this rate.
  • the temporary transfer plate with the gelled coating 8 applied to it is positioned with the coating 8 against the veneer i.
  • the various separate laminations of elements I, 2, 3, 5, E. l. 8, and the transfer plate are placed in a conventional plywood or similar hot press, such as, 'a high frequency press.
  • a conventional plywood or similar hot press such as, 'a high frequency press.
  • the reason for the above action is that the partially cured resin probably has more adhesion for the relatively coarse surface of the Wood veneer than for the smooth surface of the metal transfer plate. Also parting is aided by a slight shrinkage of the coating film, and is further encouraged by the use of a parting agent as mentioned previously. Furthermore, the partially cured film is still thermoplastic. The net result is that the veneer surface will pull the nlm off the metal surface so that a true permanent transfer is achieved at theV same time that complete polymerization of the resin occurs.
  • One or more coats 8 may be applied to the veneer. However, the second coat normally will not be applied until the preceding coat has partially dried. If desired, a clear priming coat for elasticity and toughness, or an adhesive,lmay be used between the coating 8 and the veneer However, if a proper catalyst in the correct percentages is used, a priming coat or an adhesive becomes unnecessary.
  • styrene alkyd type We have found the styrene alkyd type to be particularly effective in producing a brilliant finish.
  • Two ofthe styrene alkyds known as Selectron 5003 and Selectron 5G07, made by Pittsburgh Plate Glass Company, to which tertiary butyl hydroperoxide has been added in the above proportions produces a brilliantI finish which is perfect in transfer and in reliability of results.
  • “Solectron 5003 and 5007 can be specifically identified as conjoint copolymers of styrene and the reaction product of a dibasic acid and a polyhydric alcohol.
  • the preferred acids are phthalic, maleic, and adipic acids.
  • the preferred alcohols are glycerine, and ethylene glycol.
  • the catalyst which has produced unexpected and unlocked for results is tertiary butylhydroperoxide.
  • the critical range of tertiary butyl hydroperoxide is, ⁇ for example, approximately two parts by Weight of tertiary butyl hydroperoxide to parts by weight of styrene' alkyd.
  • Other catalysts, such benzoyl peroxide, lauroyl peroxide; para tertiary butyl perobenzoate, etc. are satisfactory but do not produce as good results.
  • polyester resins or allylresins, etc. upon heating in the presence of a catalyst, expel the solvent, if any, and change into a viscous or gel stage, after which they gradually show-a further increase Vin viscosity. If further heating :is .applied,'the massbecomes hard and nally becomes a strong, infusible, clear, colorless solid. This conversion to a thermo-hardened 'resin' ⁇ occurs without the evolution of water, ammonia, or other by-product.
  • Solvents are generally necessary for thinning the solution or dispersion to obtain adequate flow for application to a surface. ⁇ Ketones are used because they are the best solvents for the polyester resins, and because they can be relatively easily expelled from the film. If all solvent is not expelled from the nlm, poisoning takes place, and the resin will not cure.
  • the appropriate thickness range of the coating film is .008 to .015". If the film is too thick, excessive shrinkage and cracking will be experienced. If the lilm is too thin, there will be insuicient material and a hungry finish results.
  • the coating Due to the fact that the outside of the coating, particularly while it is wet and being processed, is next to and is protected by the transfer plate, the coating remains clear, clean, dust, bubble, and imperfection free. Furthermore, it photographically acquires all the perfections or imperfections in minutest detail of the surface of the transfer plate and thus will faithfully reproduce the desired type finish and degree of brilliance required by judicious choice of the type transfer plate, as well as the type resin coating q and catalyst. In other words, the polish of the transfer plate is imitated reliably. Consequently, the coating of the panel is of great brilliance due to the high refractive index of the coating and the wetting action of the resin.
  • the first type, directly applied coating is from the class of compound copolymers or polyesters of the styrene-free type, such as, a monomeric form of an organic ester of allyl alcohol and methyl methacrylate mixed in the proportion of a monomeric form of an organic ester of allyl alcohol 65% by weight and methyl methacrylate
  • the second type coating is a mixed polyester containing diallyl phthalate, such as, a -50 mixture by weight of an organic ester of allyl alcohol and a mixture of organic allyl esters to which it is unnecessary to add either styrene or methyl methacrylate.
  • the second type coating can be used in the plate transfer method as well as by direct application, but inasmuch as the direct application method produces equally satisfactorytresults for this type resin, the transfer plate method normally would not be used.
  • the transfer plate method will not work with a monomeric form of an organic ester of allyl alcohol methyl methacrylate resin so the direct application method obviously must be used.
  • Fig. 2 illustrates a modified form of our invention, in which the base material or base member I0 comprises a three-ply board having the two outer plies I and 3 of wood veneer and the center ply or core of imitation wood or synthetic wood 9, such as, Masonite, "Ceiotex,” insulation board, or a mixture of sawdust and cotton, or any other combination.
  • the metal plate is eliminated and the base veneer 'I having a heat resistant coating applied thereto is secured directly to the base member I0.
  • the high luster coating 8 could be applied to the base member as well as to the face veneer.
  • the method of applying the coating 8 to the base member would be as stated above, namely, either by applying the coating directly to the base member or by applying the coating to a transfer plate and then aiiixing it to the base member. Normally, however, the coating will be applied only to the face veneer.
  • Fig. 3 illustrates a modied form of our device in which the base member I I is formed of a one-piece synthetic wood, such as, Masonite, Celotex," wallboard, insulation board, etc. As illustrated in this iigure a metallic plate is inserted between the base member and the veneer, but no coating is applied to the veneer.
  • a metallic plate is inserted between the base member and the veneer, but no coating is applied to the veneer.
  • Fig. 4 illustrates another modified form of our invention in which a single piece of lumber, such as, of the coniferous species, is used as the base member I 2 and a veneer of inexpensive hardwood such as beech or birch is interposed'between the expensive face veneer and the base member.
  • a single piece of lumber such as, of the coniferous species
  • the metal plate 6 has two functions, namely, to shield the grain of the coniferous base and to dissipate and conduct the heat of the cigarette or hot pan away from the immediate area to other portions of the panel and thereby equalize the temperature throughout the entire panel.
  • the thin veneer of hardwood I3 serves merely to mask the grain of thebase :material from showing through to the rare or expensive face veneer.
  • metal plate 6 of Fig. 1l could be applied to Fig. 2, or could ⁇ be substituted for hardwood veneer I3 in Fig. 4.
  • element I3 of Fig. 4 could be substituted for metal plate 6 in Fig. l.
  • a cement-asbestos fiber mixture could be used in place of the metallic sheet in Fig. 1 since a cigarette will not mar the coating or the face veneer when such a ply is placed beneath the veneer and a heat resistant coating, such as, an organic ester of allyl alcohol, and a mixture of organic allyl esters to which it is unnecessary to add either styrene or methyl methacrylate is used.
  • a heat resistant coating such as, an organic ester of allyl alcohol, and a mixture of organic allyl esters to which it is unnecessary to add either styrene or methyl methacrylate is used.
  • the foregoing resins are capable of being used effectively not only in a heatproof or heat resistant construction having a metal underlay but also as a brilliant coating for any type surface.
  • the coating 8 illustrated in Fig. 2 could be applied to either the expensive hardwood veneer I4 or to the fir lumber base I2 as illustrated in Fig. 4, where the primary consideration may be to obtain a brilliant, long lasting, wear resistant 1inish and the heat resistant quality is a secondary consideration.
  • a coloring agent is very vlikely to be desirable and may on occasions be necessary. When the finish is applied to wood veneers, there will be occasions when a little color added to the top lm may be desirable to control tone.
  • the mentioned resins have great resistance to I abrasion and marring and withstand the effects of wear, Water, alcoholic beverages, etc., in a suy perior manner, while remaining remarkably clear.
  • the resins named are -inherently fire resistant to a limited extent.
  • any re retarding elements such as, sulfamic acid derivatives, ammonium bromide, ammonium phosphates, borax, zinc chloride, cellulose acetate, and mixtures of these materials may be incorporated into the resin.
  • a low pressure laminated material comprising a wood base member, a metal sheet, a wood veneer, and an ladhesive comprising polyvinyl butyral mixed with phenol formaldehyde; said base member and said veneer each being directly secured at one face thereof to an opposite surface of said metal sheet by said adhesive; and a heat resistant coating applied to the other face of said veneer and comprising approximately 65 parts by weight of a monomeric form of organic ester of allyl alcohol, approximately 35 parts by weight of methyl methacrylate, and approximately V2 parts kloy Weight of tertiary butyl hydroperoxide'.
  • a low pressure laminated material comprising a Wood base member, ⁇ a metal sheet, a wood veneer, and an adhesive comprising from approximately to approximately 75% by Weight of polyvinyl butyral mixed with from approximately 25% t0 approximately 50% by weight of phenol formaldehyde; said base member and said veneer each being .directly secured at one face thereof to an opposite surface of said metal sheet by said adhesive; and a heat resistant coating applied to the other face 0f said veneer and comprising approximately parts by weight of a monomeric form of organic ester of allyl alcohol, and approximately 35 parts by weight of methyl methacrylate, and approximately 2 parts by vweight of tertiary butyl hydroperoxide.

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  • Engineering & Computer Science (AREA)
  • Architecture (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Civil Engineering (AREA)
  • Structural Engineering (AREA)
  • Laminated Bodies (AREA)

Description

June 24, 1952 C, B, HEMMlNG ETAL 2,601,284
HEAT RESISTANT PANEL Filed Jan. 18, 1947 "NCM @Non @Mmmm o@ IN VEN T OR. GYM/H5915. #EMM/N6 RAY L. OVERHOLT BY A. hb.
Patented June 24, 1952 HEAT RESISTANT PANEL Charles B. Hemming and Ray L. Overholt, New
Rochelle, N. Y., assignors to United States Plywood Corporation, New York, N. Y., a corporation of New York Application January 1S, 1947, Serial No. 722,840
2 Claims. 1
This invention relates to the woodworking eld, and particularly to the building material industry, the furniture industry, and the fancy container industry.
One of the objects of this invention is to provide a cigarette-proof, scorchproof, or burnproof material which will withstand the heat of cigarettes indelinitely, and, also, for a short period time, will withstand the heat of hot pans, hot irons, and other hot objects, without marring the nish or the veneer proper.
Another object of this invention is to provide a surface coating which will form a high finish on the veneer and make the veneer appear extremely brilliant and glossy, while at the same time the coating itself acts as a protective shield for the wood against marring by heat and water.
Still another object of the invention is to impart a finish to a wood veneer which by combination of a high refractive index and good wetting action, i. e., excellent, intimate contact between the iilm and the veneer with resultant displacement of air, brings out the contrast and texture in startling fashion but without staining or changing the color or tone of the veneer in any way.
A fourth object of this invention is to mask the grain and checks in the relatively inexpensive base material, such as, fir, by providing a layer of metal or inexpensive hardwood between the base material and the expensive face veneer.
A fth object of this invention is to provide on a panel a surface coating having a brilliant nish produced by heating certain resins and catalysts at low temperatures for a short period of time.
Other and further objects will appear from a reading of the following specifications.
Cigarette-proof panels have been made in the past by taking a stack of thin paper sheets or rags, completely impregnating the stack with a resin, and subsequently subjecting the stack to a high pressure under heat. Large quantities of resin are expensive, and the initial cost and maintenance cost of high pressure presses, and solid, sturdy foundations and buildings to house such high pressure presses, are also expensive. In addition, the resulting product is not particularly attractive to most people because it looks artificial and lacks life. cult to produce at panels. This is the rst time, as far as is known, that a cigarette-proof or heat-proof board having a brilliant finish which sets off the grain has been made by the low pressure and, hence, inexpensive method.
Furthermore, it is dif- With the foregoing and other objects in view, the invention resides in the novel arrangement and combination of parts and in the details of construction and process of manufacture herenafter described and claimed, it being understood that changes in the precise embodiment oi the invention herein described may be made within the scope of what is claimed without departing from the spirit of the invention. It will be further understood that our invention is susceptible of embodiment in many and various forms, some of which are illustrated. in the accompanying drawing, and that the structural details or particular steps of the method herein set forth may be varied to suit particular purposes and still remain within our inventive concept.
Referring to the drawings:
Fig. 1 is a cross-sectional view of one embodiment of our invention showing not only the brilliant finish but also the metallic heat dispersing element.
Fig. 2 is a modified form of our invention illusstrating a different type base material, and having a brilliant surface coating applied to both sides of the panel. i
Fig. 3 is a further modication and discloses a different base material and a metal heat conducting material between the base and the face veneer.
Fig. Ll is a still further modication of 'our invention and shows a lumber base material and a relatively inexpensive hardwood veneer between the base material and the expensive face veneer.
A plywood panel is indicated by numeral 4 and comprises veneers I, 2 and 3. This base material is preferably iir plywood or pine plywood or some other of the inexpensive coniferous species. The basic material has been illustrated as plywood. However, even though plywood performs much better than other materials due to its great strength per unit weight, it is understood that other base materials, such as illustrated in Figs. 2, 3 or 4, may be used.
To one side ci the plywood panel a synthetic resin adhesive 5, preferably a thermosetting resin, such as, phenol formaldehyde, urea formaldehyde, melamine aldehyde, furfural resin., polyvinyl resin, or any of the synthetic rubber cements, or a mixture of phenol formaldehyde resin and butadiene acrylonitrile synthetic rubber, or a mixture of synthetic rubber derivative mixed with phenol formaldehyde resin, or other adhesive which will bind metal to wood, may be applied. However, thermosetting resins take a comparatively long time to set and are not suffrciently elastic or flexible after setting. Thermoplastic resins, on the other hand, are too elastic when set. The result of the use of the foregoing resins for a metallic plate or metallic foil to wood adhesion has been that the shrinkage of the heat resistantJ finish has caused peeling of the finish with age. These faults have been eliminated by the discovery of an intermediate adhesive which is neither strictly thermosetting nor strictly thermoplastic and might, be described as a thermosetting resin which is slightly plasticized. This new adhesive formed of polyvinyl butyral mixed with alcohol soluble, unmodified phenol formaldehyde in equal proportions by weight, or 75% polyvinyl butyral to 25% alcohol soluble, unmodied phenol formaldehyde by weight produces startling results.
An aluminum sheet or aluminum foil, a copper sheet or copper foil, a copper clad iron plate., or some other appropriate metal element 6 is placed over the adhesive and a second layer of adhesive is applied to the metallic element. Since the wood base will absorb moisture from the adhesive, in most cases it will be found advantageous to apply bothcoats of adhesive to the metal foil.
If the adhesive is applied to the metal element, both sides may be coated by one passing through the roller coating or glue spreading machine. Preferably, the adhesive should then be partially or fullydried before assembling the veneer to the metal element. Adhesive may also be applied by spraying, dipping, or other conventional ways of coating. Above the second layer of adhesive, a veneer preferably an expensive veneer, such as, teak, mahogany, etc., of the order of 1/24 inch to 175 inch, is placed.
Tothe outer side of the veneer a heat and water resistant protective coating c, of a polyester resin, such as, styrene alkyd and a catalyst is applied, The coating may be applied by spraying, dipping or otherwise coating the outer surface of the thin veneer. However, in order to obtain an exceptionally brilliant finish, the resin must be entirely free of all dirt or dust. Favorableresults may be obtained in an Vair conditioned room, but the following procedure has been found to be the best method of applying the resin to the veneer. A temporary metallic transfer plate (not shown in the drawing), preferably a chromium plated metal of some kind, such as, iron, steel, stainless steel, etc., having a smooth finish' and high polish, is rubbed liberally with a parting agent, such as, a fatty component of certain vegetable oils, such as, soy bean and castor, generally known as lethicin, carnauba wax, silicone grease, etc., and subsequently is covered with the resin coating. The temporary transfer plateA is then heated so that the resin will become firm or gelled in its intermediate stage. The time for the resin to gell is short, i. e., thirty minutes or less, and the temperature comparatively low, i. e., approximately 150 F. For example, styrene alkyd with a benzoyl peroxide lcatalyst will set in twenty minutes at 150 F. temperature, while styrene alkyd with a tertiary butyl hydroperoxide catalyst will set in ten minutes Aat 150 F. temperature. The rapidity with which the resin becomes firm is exceedingly important because the output of the plant is directly proportional to this rate.
The temporary transfer plate with the gelled coating 8 applied to it is positioned with the coating 8 against the veneer i. The various separate laminations of elements I, 2, 3, 5, E. l. 8, and the transfer plate are placed in a conventional plywood or similar hot press, such as, 'a high frequency press. After the assembly has been in the hot press for a time range of from approximately 5 to 25 minutes at approximately 300 E. and approximately 200 pounds per square inch pressure, due to the action of the catalyst which is critical in this portion of the procedure, the resinous coating leaves the metal plate and attaches securely and permanently to the veneer. There is nothing critical about the specic pressure which is used as long as it is sufficient to bond the various laminations together.
The reason for the above action is that the partially cured resin probably has more adhesion for the relatively coarse surface of the Wood veneer than for the smooth surface of the metal transfer plate. Also parting is aided by a slight shrinkage of the coating film, and is further encouraged by the use of a parting agent as mentioned previously. Furthermore, the partially cured film is still thermoplastic. The net result is that the veneer surface will pull the nlm off the metal surface so that a true permanent transfer is achieved at theV same time that complete polymerization of the resin occurs.
One or more coats 8 may be applied to the veneer. However, the second coat normally will not be applied until the preceding coat has partially dried. If desired, a clear priming coat for elasticity and toughness, or an adhesive,lmay be used between the coating 8 and the veneer However, if a proper catalyst in the correct percentages is used, a priming coat or an adhesive becomes unnecessary.
We have found the styrene alkyd type to be particularly effective in producing a brilliant finish. Two ofthe styrene alkyds, known as Selectron 5003 and Selectron 5G07, made by Pittsburgh Plate Glass Company, to which tertiary butyl hydroperoxide has been added in the above proportions produces a brilliantI finish which is perfect in transfer and in reliability of results. "Solectron 5003 and 5007 can be specifically identified as conjoint copolymers of styrene and the reaction product of a dibasic acid and a polyhydric alcohol. The preferred acids are phthalic, maleic, and adipic acids. The preferred alcohols are glycerine, and ethylene glycol. Successful applications have been made of the following other infusible and insoluble resins with appropriate catalysts: allyl esters, allyl alkyds, acrylate esters polymerized'with an alkyd ester, polyvinyl chloride-diallyl succinate, vstyrene-divinyl benzene, isobutyl urea formaldehyde, isobutyl melamine formaldehyde and other resins of these general types.
The catalyst which has produced unexpected and unlocked for results is tertiary butylhydroperoxide. The critical range of tertiary butyl hydroperoxide is, `for example, approximately two parts by Weight of tertiary butyl hydroperoxide to parts by weight of styrene' alkyd. Other catalysts, such benzoyl peroxide, lauroyl peroxide; para tertiary butyl perobenzoate, etc. are satisfactory but do not produce as good results.
The polyester resins or allylresins, etc., upon heating in the presence of a catalyst, expel the solvent, if any, and change into a viscous or gel stage, after which they gradually show-a further increase Vin viscosity. If further heating :is .applied,'the massbecomes hard and nally becomes a strong, infusible, clear, colorless solid. This conversion to a thermo-hardened 'resin' `occurs without the evolution of water, ammonia, or other by-product.
Solvents are generally necessary for thinning the solution or dispersion to obtain adequate flow for application to a surface. `Ketones are used because they are the best solvents for the polyester resins, and because they can be relatively easily expelled from the film. If all solvent is not expelled from the nlm, poisoning takes place, and the resin will not cure.
The appropriate thickness range of the coating film is .008 to .015". If the film is too thick, excessive shrinkage and cracking will be experienced. If the lilm is too thin, there will be insuicient material and a hungry finish results.
Due to the fact that the outside of the coating, particularly while it is wet and being processed, is next to and is protected by the transfer plate, the coating remains clear, clean, dust, bubble, and imperfection free. Furthermore, it photographically acquires all the perfections or imperfections in minutest detail of the surface of the transfer plate and thus will faithfully reproduce the desired type finish and degree of brilliance required by judicious choice of the type transfer plate, as well as the type resin coating q and catalyst. In other words, the polish of the transfer plate is imitated reliably. Consequently, the coating of the panel is of great brilliance due to the high refractive index of the coating and the wetting action of the resin. Good contact between the coating and the veneer takes place since there is a iiow of the coating during the transfer and the grain is therefore enhanced. The high gloss produced by the highly polished surface of the transfer plate is not diminished subsequently because the aluminum caul in the hot press is also highly polished.
The above transfer method for coating panels or other wood surface articles is, of course, longer and more expensive than spraying or brush coating the face veneer direct. However, we have found two general types of coatings which produce a brilliant heat resistant finish if applied directly to the veneer and subsequently the board is placed in a press for forming and polishing. The first type, directly applied coating, is from the class of compound copolymers or polyesters of the styrene-free type, such as, a monomeric form of an organic ester of allyl alcohol and methyl methacrylate mixed in the proportion of a monomeric form of an organic ester of allyl alcohol 65% by weight and methyl methacrylate The second type coating is a mixed polyester containing diallyl phthalate, such as, a -50 mixture by weight of an organic ester of allyl alcohol and a mixture of organic allyl esters to which it is unnecessary to add either styrene or methyl methacrylate.
The second type coating can be used in the plate transfer method as well as by direct application, but inasmuch as the direct application method produces equally satisfactorytresults for this type resin, the transfer plate method normally would not be used. The transfer plate method will not work with a monomeric form of an organic ester of allyl alcohol methyl methacrylate resin so the direct application method obviously must be used.
Fig. 2 illustrates a modified form of our invention, in which the base material or base member I0 comprises a three-ply board having the two outer plies I and 3 of wood veneer and the center ply or core of imitation wood or synthetic wood 9, such as, Masonite, "Ceiotex," insulation board, or a mixture of sawdust and cotton, or any other combination. In this modification the metal plate is eliminated and the base veneer 'I having a heat resistant coating applied thereto is secured directly to the base member I0.
If desired, the high luster coating 8 could be applied to the base member as well as to the face veneer. The method of applying the coating 8 to the base member would be as stated above, namely, either by applying the coating directly to the base member or by applying the coating to a transfer plate and then aiiixing it to the base member. Normally, however, the coating will be applied only to the face veneer.
Fig. 3 illustrates a modied form of our device in which the base member I I is formed of a one-piece synthetic wood, such as, Masonite, Celotex," wallboard, insulation board, etc. As illustrated in this iigure a metallic plate is inserted between the base member and the veneer, but no coating is applied to the veneer.
Fig. 4 illustrates another modified form of our invention in which a single piece of lumber, such as, of the coniferous species, is used as the base member I 2 and a veneer of inexpensive hardwood such as beech or birch is interposed'between the expensive face veneer and the base member.
In cases where coniferous wood such as `fir lumber or fir plywood is used asthe base material, the grain of this base material will show through the thin outer Veneer unless an intermediate sheet is interposed in order to mask this grain raising of the hard and soft grain of the summer and spring growth of the base material. Therefore, the metal plate 6 has two functions, namely, to shield the grain of the coniferous base and to dissipate and conduct the heat of the cigarette or hot pan away from the immediate area to other portions of the panel and thereby equalize the temperature throughout the entire panel.
In Fig. 4 the thin veneer of hardwood I3 serves merely to mask the grain of thebase :material from showing through to the rare or expensive face veneer.
It is understood that the drawing is only illustrative of the invention. For example, metal plate 6 of Fig. 1l could be applied to Fig. 2, or could `be substituted for hardwood veneer I3 in Fig. 4. Likewise, element I3 of Fig. 4 could be substituted for metal plate 6 in Fig. l. Also, a cement-asbestos fiber mixture could be used in place of the metallic sheet in Fig. 1 since a cigarette will not mar the coating or the face veneer when such a ply is placed beneath the veneer and a heat resistant coating, such as, an organic ester of allyl alcohol, and a mixture of organic allyl esters to which it is unnecessary to add either styrene or methyl methacrylate is used. Furthermore, in certain cases it may be desirable to dispense with the base member and use only the metal plate and the veneer, with or without the coating.
It is also understood that the foregoing resins are capable of being used effectively not only in a heatproof or heat resistant construction having a metal underlay but also as a brilliant coating for any type surface. For example, the coating 8 illustrated in Fig. 2 could be applied to either the expensive hardwood veneer I4 or to the fir lumber base I2 as illustrated in Fig. 4, where the primary consideration may be to obtain a brilliant, long lasting, wear resistant 1inish and the heat resistant quality is a secondary consideration.
Mixed synthetic resin-synthetic elastomer or high polymer adhesivesV are mentioned as being preferable Where a: metal plate is used. However, any of the less expensive common phenol formaldehydes, urea formaldehydes, or melamine resins, in solvents of Water, alcohol, or acetone, may be used in the construction as illustrated by I in Fig. 4. Also, a dry lm glue, such as, tissue paper or other thin paper impregnated with an appropriate resin, might be used. The hardwood veneer I3 does need to be grade A, but can be of a poor quality both as to soundness and color.
A coloring agent is very vlikely to be desirable and may on occasions be necessary. When the finish is applied to wood veneers, there will be occasions when a little color added to the top lm may be desirable to control tone.
The mentioned resins have great resistance to I abrasion and marring and withstand the effects of wear, Water, alcoholic beverages, etc., in a suy perior manner, while remaining remarkably clear. The resins named are -inherently fire resistant to a limited extent. However, if desired, any re retarding elements, such as, sulfamic acid derivatives, ammonium bromide, ammonium phosphates, borax, zinc chloride, cellulose acetate, and mixtures of these materials may be incorporated into the resin.
It can thus be seen that we have invented a new and extremely saleable, heatproof material for room construction, elevator cabs, table tops, furniture generally, etc., having a very striking and brilliant nish, which can be taken from the press While the press is hot, will resist wearing and marring to a great extent, and `which will not `sweat when a cigarette cr other hot object is placed thereon. As a building material, the exquisite finish will be desirable and inherently thematerial will tend to be re resistant.
What We claim is:
l. As a new article of manufacture, a low pressure laminated material comprising a wood base member, a metal sheet, a wood veneer, and an ladhesive comprising polyvinyl butyral mixed with phenol formaldehyde; said base member and said veneer each being directly secured at one face thereof to an opposite surface of said metal sheet by said adhesive; and a heat resistant coating applied to the other face of said veneer and comprising approximately 65 parts by weight of a monomeric form of organic ester of allyl alcohol, approximately 35 parts by weight of methyl methacrylate, and approximately V2 parts kloy Weight of tertiary butyl hydroperoxide'.
2. As a new article of manufacture, a low pressure laminated material comprising a Wood base member, `a metal sheet, a wood veneer, and an adhesive comprising from approximately to approximately 75% by Weight of polyvinyl butyral mixed with from approximately 25% t0 approximately 50% by weight of phenol formaldehyde; said base member and said veneer each being .directly secured at one face thereof to an opposite surface of said metal sheet by said adhesive; and a heat resistant coating applied to the other face 0f said veneer and comprising approximately parts by weight of a monomeric form of organic ester of allyl alcohol, and approximately 35 parts by weight of methyl methacrylate, and approximately 2 parts by vweight of tertiary butyl hydroperoxide.
CHARLES B. ,HEMM'ING,. RAY L. OVERHOLT.
REFERENCES. CT ED The following references are of record in the iile or"v this patent:
UNITED STATES PATENTS Number Name Date 1,019,408 Baekeland et al. Mar. 5, 1912 1,824,690 Schneider Sept. 22, 19.31 1,972,307 Loetscher Sept. 4, 1934 2,011,130 Ward Aug. 1 3, 1935 2,256,108 Blake Sept. 1,6, 19,41 2,273,891 Pollack et al Feb. k24, 1942 2,306,295 Casto Dec. 22, A1942 2,396,098 Haas Mar. 5, 1946 2,401,281 Y Webb May 28, 1946 2,419,614 'Welch Apr. 29, 1947 2,431,374 DAlelo Nov. 25, 1947 2,443,740 Kropa June 22, 1948 2,444,655 Kroeker et al. July 6, 1948 FORElGN 'PATENTS Number l Country Date .fi-40.5.7.8 Great Britain Jan. ,2. 1.936

Claims (1)

1. AS A NEW ARTICLE OF MANUFACTURE, A LOW PRESSURE LAMINATED MATERIAL COMPRISING A WOOD BASE MEMBER, A METAL SHEET, A WOOD VENEER, AND AN ADHESIVE COMPRISING POLYVINYL BUTYRAL MIXED WITH PHENOL FORMALDEHYDE; SAID BASE MEMBER AND SAID VENEER EACH BEING DIRECTLY SECURED AT ONE FACE THEREOF TO AN OPPOSITE SURFACE OF SAID METAL SHEET BY SAID ADHESIVE; AND A HEAT RESISTANT COATING APPLIED TO THE OTHER FACE OF SAID VENEER AND COMPRISING APPROXIMATELY 65 PARTS BY WEIGHT OF A MONOMERIC FORM OF ORGANIC ESTER OF ALLYL ALCOHOL, APPROXIMATELY 35 PARTS BY WEIGHT OF METHYL METHACRYLATE, AND APPROXIMATELY 2 PARTS BY WEIGHT OF TERTIARY BUTYL HYDROPEROXIDE.
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2745779A (en) * 1952-10-11 1956-05-15 Ritter Eugen Johann Method of making laminated panels and product thereof
US3013914A (en) * 1958-03-11 1961-12-19 Du Pont Terephthalic acid copolyester compositions
US3027291A (en) * 1957-09-09 1962-03-27 Diamond Alkali Co Composition and method of preventing adhesion
US3076773A (en) * 1958-10-17 1963-02-05 Diamond Alkali Co Aqueous emulsion of an organic solvent-siloxane mixture
US3087566A (en) * 1958-12-30 1963-04-30 Bolt Beranek & Newman Soundproofing panel structure
US3511731A (en) * 1966-05-25 1970-05-12 Panneaux Landais Sopaland Soc Composite panel and an improved manufacturing method therefor
US3981537A (en) * 1975-05-21 1976-09-21 Champion International Corporation Person's body weight support in furniture assembly
US4165409A (en) * 1978-02-23 1979-08-21 Jack Maine Method of fabricating wood composite panels having enhanced fire retardancy
US4272581A (en) * 1978-10-06 1981-06-09 James Cooley Heat resistant decorative laminate
WO2003072351A1 (en) * 2002-02-21 2003-09-04 Murcia Philippe R Composite material paneling and method of making same
US20120067508A1 (en) * 2006-10-10 2012-03-22 Booth Carl F Fire resistant veneer assembly for aircraft interiors
WO2014031528A3 (en) * 2012-08-21 2014-05-22 Milwaukee Composites, Inc. Flooring assembly with heat dissipation layer

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US1824690A (en) * 1931-09-22 Method of coating fabrics with cellulose derivatives
US1972307A (en) * 1932-02-02 1934-09-04 Emil C Loetscher Uniting synthetic resin and metal
US2011130A (en) * 1932-03-16 1935-08-13 Neil C Ward Burnproof material
GB440578A (en) * 1933-10-16 1936-01-02 Formica Insulation Company Improvements in heat-dissipating laminated products and in processes for their production
US2256108A (en) * 1938-07-26 1941-09-16 Polaroid Corp Process for transferring lightpolarizing films from one support to another
US2273891A (en) * 1939-02-18 1942-02-24 Pittsburgh Plate Glass Co Method of polymerizing polymerizable materials containing more than one polymerizable grouping
US2306295A (en) * 1939-05-04 1942-12-22 Lloyd V Casto Method of making laminated furniture panels
US2401281A (en) * 1942-04-10 1946-05-28 Oscar H Webb Composite structure
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US2431374A (en) * 1943-12-30 1947-11-25 Pro Phy Lac Tie Brush Company Copolymers of diallyl maleate and saturated monohydric alcohol esters of maleic and fumaric acids
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2745779A (en) * 1952-10-11 1956-05-15 Ritter Eugen Johann Method of making laminated panels and product thereof
US3027291A (en) * 1957-09-09 1962-03-27 Diamond Alkali Co Composition and method of preventing adhesion
US3013914A (en) * 1958-03-11 1961-12-19 Du Pont Terephthalic acid copolyester compositions
US3076773A (en) * 1958-10-17 1963-02-05 Diamond Alkali Co Aqueous emulsion of an organic solvent-siloxane mixture
US3087566A (en) * 1958-12-30 1963-04-30 Bolt Beranek & Newman Soundproofing panel structure
US3511731A (en) * 1966-05-25 1970-05-12 Panneaux Landais Sopaland Soc Composite panel and an improved manufacturing method therefor
US3981537A (en) * 1975-05-21 1976-09-21 Champion International Corporation Person's body weight support in furniture assembly
US4165409A (en) * 1978-02-23 1979-08-21 Jack Maine Method of fabricating wood composite panels having enhanced fire retardancy
US4272581A (en) * 1978-10-06 1981-06-09 James Cooley Heat resistant decorative laminate
WO2003072351A1 (en) * 2002-02-21 2003-09-04 Murcia Philippe R Composite material paneling and method of making same
US20120067508A1 (en) * 2006-10-10 2012-03-22 Booth Carl F Fire resistant veneer assembly for aircraft interiors
WO2014031528A3 (en) * 2012-08-21 2014-05-22 Milwaukee Composites, Inc. Flooring assembly with heat dissipation layer
US9567754B2 (en) 2012-08-21 2017-02-14 Milwaukee Composites, Inc. Flooring assembly with heat dissipation layer

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