EP0138809B1 - Stempeldekor mittels hitzeübertragung und dessen substrate - Google Patents

Stempeldekor mittels hitzeübertragung und dessen substrate Download PDF

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Publication number
EP0138809B1
EP0138809B1 EP19830901669 EP83901669A EP0138809B1 EP 0138809 B1 EP0138809 B1 EP 0138809B1 EP 19830901669 EP19830901669 EP 19830901669 EP 83901669 A EP83901669 A EP 83901669A EP 0138809 B1 EP0138809 B1 EP 0138809B1
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EP
European Patent Office
Prior art keywords
layer
laminate
article
substrate
transfer
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Expired
Application number
EP19830901669
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English (en)
French (fr)
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EP0138809A1 (de
EP0138809A4 (de
Inventor
Mary G. Boyd
Donald R. Smith
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dennison Manufacturing Co
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Dennison Manufacturing Co
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Publication date
Application filed by Dennison Manufacturing Co filed Critical Dennison Manufacturing Co
Priority to AT83901669T priority Critical patent/ATE36280T1/de
Publication of EP0138809A1 publication Critical patent/EP0138809A1/de
Publication of EP0138809A4 publication Critical patent/EP0138809A4/de
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Publication of EP0138809B1 publication Critical patent/EP0138809B1/de
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B44—DECORATIVE ARTS
    • B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
    • B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
    • B44C1/16—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like
    • B44C1/165—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like for decalcomanias; sheet material therefor
    • B44C1/17—Dry transfer
    • B44C1/1712—Decalcomanias applied under heat and pressure, e.g. provided with a heat activable adhesive
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65C—LABELLING OR TAGGING MACHINES, APPARATUS, OR PROCESSES
    • B65C9/00—Details of labelling machines or apparatus
    • B65C9/20—Gluing the labels or articles
    • B65C9/24—Gluing the labels or articles by heat

Definitions

  • the present invention relates to heat transfer decoration, as well as to the decoration of objects using a deformable pad.
  • the invention further relates to the design of labels transferable by these methods.
  • a widely employed prior art method for imprinting designs onto articles using a heat transfer labelling process employs a paper base sheet or web coated with a label consisting of a release layer over which a design is imprinted in ink.
  • labels of the above description are transferred to bottles or other articles using heat and pressure by feeding the article to a transfer site, where the preheated label-bearing web is impressed against the bottle to transfer the label.
  • Patents illustrative of the above method and apparatus commonly assigned with the present application, include U.S. Patent Nos. 2,981,432, 3,064,714; 3,079,979; 3,208,897, 3,231,448, 3,261,734; and 4,214,937.
  • pad-transfer decorator Another type of apparatus which possesses special advantages in the decoration of objects of unusual conformation is the so-called pad-transfer decorator.
  • This apparatus utilizes a deformable pad, typically comprised of a silicone elastomer.
  • the pad receives an ink impression to be transferred to an article by pressing against an intaglio plate which had been previously coated with ink with any excess ink removed.
  • the invention-bearing pad is then pressed against the article to be labelled, to which it imparts the ink impression.
  • the deformable pad is adaptable to a wide variety of article conformations.
  • This decorative method and apparatus involves assembly-line equipment of a simpler design than the above-discussed heat-tranfer decorators, and therefore requires fewer adjustments in retooling to articles of a variety of sizes and shapes. However, this process only transfers one color of ink at a time, and is thus slow and cumbersome if multicolored designs are required. Also, since there is no protective coating covering the ink design, it
  • U.S. Patent No. 3,887,420 discloses the use of a silicone rubber pad to transfer designs from a decorative laminate to ceramic articles.
  • the laminate includes a base layer such as a paper sheet overlayed with a coating of wax.
  • the wax coating is coated with a film layer (Film B), which in turn is overcoated with an ink design layer and a second film (Film A).
  • Film B is alleged to become adhesive while the wax coating and Film B become molten and nonadhesive.
  • the transfer pad purportedly sticks to Film A when it is pressed against the laminate so that as the transfer pad is withdrawn, the substrate compposed of the paper sheet and wax coating separates from ths remainder of the laminate.
  • the laminate adhering to the transfer pad is pressed onto a ceramic article, and the temperature of the laminate is dropped to within a narrow 5.6°C (10°F) temperature range. At this temperature, Film B becomes adhesive and Film A is alleged to exhibit diminished adhesion.
  • the laminate is alledged to adhere to the article and released from the transfer pad as the pad is withdrawn.
  • the film layers A and B are each adhesive over only a very narrow 5.6°C (10°F) temperature range, making it impracticable to control the described process within the context of an automated process, since each film layer most in turn be heated or cooled to within the required 5.6°C (10°F) temperature range to make the process workable. Precise heating or cooling of Film A and Film B to within such narrow temperature ranges is impossible to acheive or control within the split second time intervals required by an automated assembly process.
  • This reference does not disclose the use of an independent pad heater, nor details of pad composition, surface texture, or other parameters crucial to its implementation.
  • the inclusion of a wax layer to form part of the decorative substrate has the disadvantage that as the substrate is released from Film B there will be a strong tendency for a portion of the wax to remain attached to Film B. This will interfere with the adhesive characteristics of Film B as the laminate is transferred from the transfer pad to an object.
  • U.S. Patent No. 3,616,176 discloses a heat transfer laminate of a type related to that disclosed in U.S. Patent 3,616,015.
  • the laminate is composed of a base sheet, with a polyamide layer covering the base sheet and a decorative ink layer covering the polyamide layer.
  • Sufficient heat is applied to the laminate to heat the polyamide layer at or above its softening point, and the laminate is then pressed onto the surface of an article with the decorative ink layer coming into direct contact.
  • the polyamide layer cools to a temperature below its softening point and the base sheet is removed.
  • the decorative layer becomes fused or heat sealed to the article.
  • Another object of the invention is that the technique be readily adapted to rapid and efficient operation.
  • a related object is a multicolored decoration capability without the need for successive decorative stages.
  • Yet another object of the invention is the provision of a decorative process which is adaptable to a variety of articles. Such technique, for example, should be suited to the decoration of plastic, glass, and ceramic articles.
  • Still another object of the invention is the achievement of high quality decoration of articles.
  • the method of the invention should impart a desired image completely and without significant distortion.
  • a particular object in this regard is the provision of high glass images.
  • a further object of the invention is the provision of durable, reasonably inexpensive decoration.
  • Another object of the invention is to provide a method adapted for use with a decorative laminate which achieves -multicolor pad transfer decoration in a single transfer operation.
  • Another object of the invention is to provide such a method for use with a decorative laminate which permanently adheres to any articles without subsequent firing of the laminate.
  • a further object of the invention is to achieve a pad transfer method which satisfies the above criteria while being compatible with automated operation.
  • Yet another object of the invention is to provide an improved method, by the use of a particular type of resinous adhesive/release layer, which yields both very favourable release of the laminate from the support and also adhesion of the laminate to a receiving article.
  • a method of transferring a decorative laminate from a support to an article comprising a resinous adhesive/release layer in contact with the support, there being no intermediate wax-based release layer between the adhesive/release layer and the support, and a design layer; the method comprising heating the laminate to a first temperature above the melting point of the adhesive/release layer by applying heat to the support; heating the surface of an elastomeric member to a second temerature below the first temperature; contacting the laminate under pressure with the heated elastomeric member so that the laminate adheres to the elastomeric member and separates from the support upon withdrawal of the elastomeric member; impressing the laminate against the article to bond the adhesive/release thereto; and withdrawing the elastomeric member from the article, whereupon the laminate remains adhered to the article; characterised in that the adhesive/release layer comprises a polyamide which is the polymerization product of a diamine with a dimerized fatty acid.
  • the transfer substrate includes an adhesive/release layer which is softened by the heating of the support member and separated therefrom during the first transfer.
  • This layer also functions as an adhesive, forming a permanent bond to the article during the second transfer.
  • the transfer substrate further includes an ink design layer over the adhesive layer.
  • the substrate includes a protective coating layer over the ink layer; this layer may be omitted in many applications.
  • the transfer substrate further includes a barrier layer intermediate the adhesive/release layer and the ink layer.
  • the barrier layer where included, functions to prevent absorption of ink into the resinous coating.
  • the invention has the advantage that the transfer substrate may be composed of either a single colored decorative design or a multicolored decorative design including halftone colors. Another advantage of the invention is that the transfer substrate may be transferred to virtually any type of article irrespective of its shape or degree of surface curvature without causing distortion to the design imprint.
  • the article may, for example, be composed of ceramic, glass, plastic, paper foil, and a variety of polymeric materials, and the surface to which the transfer substrate is transposed may be flat or include compound curves, irregular surfaces, or recessed panels.
  • a preferred decorative lamiante for use with the method of the invention includes a paper sheet or web, which is coated on one side with the various layers constituting the transfer substrate.
  • the transfer substrate includes a resinous coating layer in contact with the support (i.e. the adhesive/release layer), an ink layer covering the resinous coating layer and a protective coating layer over the ink layer.
  • the barrier layer where included is of the same composition as the protective coating.
  • the adhesive/release layer includes a plasticizer such as castor oil, which may be modified by the addition of erucamide (a fatty amide of cis-13-decosenoic acid).
  • a plasticizer such as castor oil
  • erucamide a fatty amide of cis-13-decosenoic acid
  • Particularly favourable properties are achieved in this layer when it comprises at least 80 percent by weight polyamide resin, the balance being a plasticizer.
  • Additional plasticizer may be included in the formulation of the adhesive/release layer to increase its fluidity.
  • erucamide is included in the adhesive/release layer the above-mentioned proportions are suitably adjusted so that the polyamide resin comprises at least 70 percent of the formulation, more preferably between 70 and 90 percent.
  • the ratio of plasticizer to erucamide is in the range 5/1 to 15/1.
  • the preferred polyamide resin is composed of the polymerization product of a linear methylene diamine and dimerized fatty acid.
  • Specific polyamide resins which have been found to be particularly suitable are the polymerization products of hexamethylene diamine and dimerized linoleic acid, and tetramethylene diamine and dimerized oleic acid.
  • a preferred plasticizer is castor oil.
  • Alternative plasticizers may include rosin esters, chlorinated paraffins, aliphatic esters, epoxy esters, alkyl aromatic phthalates, glycol esters, and alkyl aromatic phosphates.
  • a preferred composition for the dried protective coating and optional barrier layer consists of the combination of a polymer (i) which is a film forming, multiaromatic, acid-based polyester, preferably linear which is reinforced by a second polymer (ii) containing bulky ring structures such as polymerized rosin esters.
  • the multiaromatic acid-based polyester (Polymer (i)) should comprise between about 50 to 80 percent by weight of the dried protective coating layer or the optional barrier layer with the polymerized rosin ester (Polymer (ii)) comprising the balance of the mixture, i.e. between about 20 to 50 percent by weight.
  • the multiaromatic acid-based polyester (Polymer (i)) is preferably composed of the polymer condensation products of polyester forming reactants of one or more glycols reacted with naphthalic or phthalic acids.
  • a preferred rosin ester (Polymer (ii)) is formed typically of the reaction product of a polyhydric alcohol, maleic anhydride or phenol aldehyde reacted with rosin acids such as abietic and pimaric acids.
  • the rosin ester (Polymer (ii)) is preferably composed of methyl abietate, methyl hydroabietate, glyceryl hydroabietate or ester gum.
  • the ink layer may be composed of a single colored ink or may include a multiplicity of differentily colored inks.
  • the ink may be composed of any conventional nitrocellulose ink, preferably a polyamide- nitrocellulose ink.
  • inks having an acrylic polyester, or vinyl base are also particularly suitable.
  • the ink layer is preferably composed of an isobutyl methacrylate ink modified with maleic rosin and polyisoprene.
  • inks having a polyamidenitrocellulose or vinyl base may be adopted if the substrate does include a protective layer.
  • the basis weight of the dried resinous coating layer may advantageously fall in the range 0.68­6.8 kg (1.5 to 15 Ibs)/ream, and the dried protective coating layer or barrier layer from about 0.22-1.36 kg (0.5 to 3 Ibs)/ream, (2.79 m 2 (3000 sq. ft.) per ream).
  • heat is conducted through an exposed undersurface of a support web, supplied from a heated platen or the like. Sufficient heat is supplied to tackify the protective coating layer (or ink layer, where the protective coating is omitted) and to soften and begin to melt the adhesive/release layer. As a result, the protective coating adheres to the surface of the transfer pad, and the softened resinous coating is released from the support web.
  • a suitable platen temperature to achieve the above objects is in the range 166­216°C (330°F to 420°F), more preferably between 171-193°C (340°F and 380°F), for automatic operation.
  • the transfer pad is heated to a surface temperature around 56-111°C (100°F-200°F) lower than the platen's temperature.
  • the heating of the transfer pad occurs as a natural result of the label pick-up process whereby the pad at least indirectly contacts the heated platen.
  • the heated pad serves to maintain the adhesive/release layer in a softened, tackified state and permits the eventual release of the transfer substrate.
  • An illustrative temperature range is between about 66-149°C (150°F-300°F). The various temperatures are dependent on the mechanical design of the transfer apparatus, and will tend to be lower for a given label chemistry with higher transfer pressures and lower cycle speeds.
  • a preferred composition for the transfer pad is an elastomeric material.
  • Silicone rubber has the advantages of being easily molded in a variety of configurations, and having suitable deformability as known in the prior pad transfer art. In the present invention, this material enjoys the aditional significant advantage of withstanding the elevated temperatures which are characteristic of the transfer process.
  • a particular property of some importance in the transfer of smooth, glossy labels is that the pad surface have a relatively smooth texture.
  • the decorative laminate 5 of the invention is composed of a support 10, typically a substrate composed of a paper sheet or web which is affixed at least on one side to a transfer substrate 7.
  • Transfer substrate 7 as best shown in Figures 1 and 2, is preferably composed of a resinous coating layer 20, an ink layer 30 and a protective coating 40.
  • the laminate 5 and substrate 7 may include a barrier layer 25 between ink layer 30 and resinous coating 20.
  • Laminate 5 is formed by providing support 10 with a resinous coating 20 on at least one side of support 10. Resinous coating 20 is overcoated with an ink layer 30 composed of letters or designs imprinted in ink. Ink layer 30 is in turn provided with an overcoating of protective coating layer 40.
  • the transfer substrate 7 may also be provided with a resinous barrier coating between ink layer 30 and resinous coating 20.
  • the barrier coating 25 illustrated in Figure 3 may typically be of the same comopsition as protective coating 40 and prevents absorption of the ink into the resinous coating 20.
  • Use of a protective coating layer 40 is particularly advantageous when the container contents includes corrosive or abrasive elements such as alcohol, cosmetics, toiletries, food and dairy products, beverages or frozen goods.
  • the protective coating layer 40 may be omitted from the transfer substrate 7 as illustrated in Figures 4 and 5.
  • Protective coating layer 40 may be omitted in labelling applications, particularly wherein the transfer substrate 7 will not be exposed to harsh chemicals or corrosive elements, for example when applied to tags or containers holding chemically inactive material.
  • the transfer substrate 7 may be composed of resinous coating 20 overcoated with an ink layer 30 as illustrated in Figure 4.
  • the transfer substrate 7 without a protective coating layer is affixed to support 10 as shown in Figure 4 to form a decorative laminate 5.
  • a barrier layer 25 may be included between ink layer 30 and resinous coating 20 to form a transfer substrate 7 as illustrated in Figure 5 which does not have a protective coating layer. The barrier layer 25 prevents absorption of the ink into the resinous coating 20.
  • the laminate of the invention is particularly suitable for use in automated processes.
  • a support 10 typically in the form of a web carrying a plurality of transfer substrate 7 aligned in single rows are passed under a flexible transfer pad 50.
  • the transfer pad 50 preferably composed of silicon rubber and support substrate 10 are each first heated. Transfer pad 50 is then pressed onto substrate 7 as it is passed under the pad 50 so that the pad comes into contact with the protective coating layer 40 or ink layer 30 if the substrate 7 does not include a protective layer 40. As the transfer pad 50 is withdrawn, substrate 7 adheres to the pad and the support 10 separates from substrate 7. Substrate 7 is then pressed onto an article so that the resinous coating layer 20 contacts the article.
  • substrate 7 As the transfer pad 50 is withdrawn it separates from substrate 7, and substrate 7 adheres to the article. A permanent bond between resinous coating layer 20 and the article then forms. If substrate 7 includes a protective coating 40, the ink design in ink layer 30 is distinctly visible through protective coating 40 after substrate 7 has been transferred to the article. Protective coating 40 dries to a smooth, glossy finish which protects ink layer 30 from the environment.
  • the first step of the process sufficient heat is applied to the exposed surface of support 10, to heat the substrate to a temperature which is above the melting point of the resinous coating 20.
  • Support 10 is heated to a temperature typically between about 28-83°C (50°F to 150°F) above the melting point of the resinous coating 20.
  • support 10 is heated to between about 166 ⁇ 216°C (330°F to 420°F), more preferably 171-182 0 C (340°F-360°F), so that the protective coating 40 (or ink layer 30, if protective coating is not included in substrate 7) becomes tacky, and resinous coating 20 softens and begins to melt enough the permit the support to be removed from transfer substrate 7.
  • the rubber transfer pad 50 preferably composed of silicon rubber, having a smooth contact surface is heated to a temperature which is lower than the temperature to which support 10 is heated, preferably 56-111°C (100° to 200°F) lower than the temperature of support 10.
  • the transfer pad 50 is heated to between about 66­149°C 150°F to 300°F, more preferably 66-121°C (150°F-250°F).
  • the various disclosed temperatures are dependent on the mechanical characteristics of the transfer apparatus as well as the label chemistry and will generally be lower at higher transfer pressures and lower cycle speeds.
  • Transfer pad 50 will be heated as a normal incident of the transfer process, inasmuch as it will periodically, at least indirectly, contact the means for heating support 10. If this heating effect is insufficient in the context of a given system, an independent heater should be provided for pad 50.
  • the hot transfer pad 50 is pressed against laminate 10 so as to make pressure contact with the protective coating 40 or ink layer 30 in the event protective coating 40 is omitted.
  • the transfer pad is then withdrawn as shown in Figure 2, at which time coating 20 splits to separate from support 10 thus releasing support 10.
  • the coating 40 or ink layer 30 is sufficiently adhesive that the substrate 7 adheres to the transfer pad.
  • the substrate 7 is left in adhesive contact with the transfer pad 50 and resinous coating 20 is exposed to the environment.
  • the hot transfer pad 50 and adhering substrate 7 is then pressed onto a surface of either a flat or three-dimensional object including articles having compound curves, irregular surfaces, or recessed panels so that the exposed coating layer 20 comes into pressure contact with the article.
  • the article may consist of any of a wide range of materials including ceramic, plastic, or glass.
  • the time interval between steps three and four is preferably less than about 5 seconds, more preferably between about 0.2 to 5 seconds.
  • coating 20 will be sufficiently tacky up to temperatures from about 66-149°C (150-300°C).
  • coating 20 As coating 20 comes into contact with article 60, it exhibits a tacky adhesive quality which is greater than the adhesive force between substrate 7 and transfer pad 50.
  • Pad 50 is withdrawn from article 60 in a fifth step of the process.
  • the time interval between the moment of contact of substrate 7 with the article and the moment of withdrawal of pad 50 away from the article is preferably less than about 1 second and as low as about 0.2 second, preferably between 0.2 and 0.5 second.
  • Coating 20 also functions to permanently bond substrate 7 to the article as the substrate is left to dry under ambient conditions.
  • the resinous coating layer 20 may be termed an "adhesive/release” layer, in that it provides the dual functionality as a release layer to permit separation of substrate 10 in one step of the process, and ultimately as a permanent adhesive to bond the ink layer 30 to an article.
  • protective coating 40 when included in the substrate forms a hard, protective lacquer coating over ink layer 30 forming a chemical and abrasion resistant protective layer, thus sealing the ink layer from exposure to moisture vapor, oxygen, grease, and other corrosive elements in the environment.
  • the resulting laminate has the property that the design, which may be either a single or multiple colored design, shows distinctly therethrough regardless of the type of curvature of the surface to which it has been applied and regardless of whether the article is composed of ceramic, glass, or plastic.
  • the outline of the protective coating layer 40 or the resinous coating 20 on the article is essentially invisible to normal inspection.
  • the coating layer 20 and protective coating 40 remain permanently affixed to article 60 as an integral part of the transfer substrate.
  • ink layer 30 is exposed directly to the environment.
  • the affixed substrate is not subjected to firing, but it should be appreciated that if article 60 is composed of glass, an inorganic flux material may be added to form ink layer 30. In this case, if substrate 7 is exposed to high temperature firing, the organic layers 20 and 40 are volatilized leaving ink layer 30 fused to the article.
  • compositions of the respective layers comprising the decorative laminate 7 are set forth as follows with reference made to the accompanying tables.
  • the support 10 may be any support member or web to hold imprint substrate 7 securely attached thereto. However, it is preferable to have support 10 composed of a paper sheet more preferably a paper sheet that is clay-coated to improve its smoothness quality and to retard penetration of the resinous coating 20 into the paper sheet as heat is applied to the back of the paper.
  • the paper sheet may be any type of paper preferably Kraft-type paper having a thickness of between about 0.05-0.06 mm (2 to 2.5 mils) and a basis weight of between about 12-18 kg (26 to 40 Ibs)/ream (279 m 3 (3000 sq. ft.) per ream).
  • Goating layer 20 is preferably composed of a polyamide resin having a softening point advantageously between about 96°C ⁇ 105°C.
  • the polyamide resin is preferably composed of the polymerization product of a linear methylene diamine and dimerized fatty acid.
  • a polyamide resin which has been determined to be particularly advantageous is the polymerization products of hexamethylene diamine and dimerized linoleic acid, and tetramethylene diamine and dimerized oleic acid.
  • Table I is particularly suitable for resinous coating layer 20, since it has been discovered to have the required release properties permitting the easy removal of substrate 10 in one step of the process and ultimately as a permanent adhesive to bond ink layer 30 to article 60 in another step as discussed in the foregoing.
  • the coating layer 20 is made preferably by admixing the components shown in Table I in the weight proportions by weight indicated in Table I to form a polyamide resinous solution.
  • the mixture is prepared at ambient temperature and utilizing conventional mixing equipment.
  • the preferred polyamide resin shown in Table I is sold under the tradename EMEREZ 1537 by Emery Industries of Cincinnati, OH.
  • the polyamide resin EMEREZ 1537 is the polymerization product of the type above-mentioned, namely, the product of a methylene diamine such as hexamethylenediamine and a dimerized fatty acid such as dimerized linoleic acid. It has a softening point between 110 to 120°C, a viscosity at 160°C of 3.5 to 5.0 poise (0.35 to 0.5 Pa.s) a Gardner color index (max.) of 4.0, an acid value of 4.0 max., and density at 25°C of 8.1 lbs./gal. (0.97 kg per litre).
  • the resinous solution is typically prepared by dissolving the polyamide resin EMEREZ 1537 in isopropyl alcohol and toluene in the proportions indicated in Table I and then modifying the resulting solution with about 4 to 16 percent by weight castor oil plasticizer and further by the addition of 2 to 8 percent by weight of erucamide (e.g. Kanamide E).
  • erucamide e.g. Kanamide E
  • the resulting polyamide resinous dispersion has a typical preferred composition as set forth in Table I.
  • Erucamide is a fatty amide of cis-13- decosenoic acid sold under the tradename KENAMIDE E by Humko Sheffield Chemical Div. of Kraftco Corp., Memphis, TN.
  • the erucamide additive permits the use of an increased amount of castor oil plasticizer which enhances the fluidity of the resinous coating layer.
  • the fatty amide KENAMIDE-E has an average molecular weight of 335, an iodine value between about 70 to 80, a capillary melting point of about 76 to 86°C and a Gardner color maximum of 5.
  • the polyamide resinous solution having a typical composition illustrated in Table I may be applied to the support 10 by any conventional printing method, for example, by gravure, silk screen, offset, or flexographic printing methods.
  • the gravure method is preferred because better process print can be realized by this method as well as better economy and color consistency with long runs.
  • the solvents are evaporated and the resulting dried resinous coating (20) has a typical preferred composition as shown in Table I.
  • the dried resinous coating (20) covering support 10 has a basis weight preferably of between about 0.68-6.8 kg (1.5 to 15 Ibs.)/ream, more preferably between about 1.4-2.3 kg (3 to 5 lbs.)/ream (279 m 2 (3000 sq. ft.) per ream) and has a melt viscosity in the range of 0.35-0.85 Pa.s (3.5 to 8.5 poise) at 160°C.
  • Ink layer 30 may be composed of any conventional type of ink of any color including halftone colors.
  • the inks which are preferable have the property that they do not soak into the resinous coating when applied without a barrier layer.
  • the present invention has the advantage that multicolored inks can be used to produce a multicolored design image, that is, multicolored design images transferable in one pass.
  • a preferred ink is a polyamide-nitrocellulose ink.
  • the polyamide is a dimerized fatty acid copolymerized with a linear diamine which constitutes about 80 weight percent of the ink and the remainder is essentially nitrocellulose.
  • Alternative inks having an acrylic, polyester, or vinyl base may also be employed.
  • ink layer 30 is preferably composed of an isobutyl methacrylate-type ink which exhibits suitable adhesive and release characteristics to allow substrate 7 to be transferred to pad 50 and thence released therefrom as substrate 7 is pressed onto an article.
  • a preferred ink of this type has been determined to be an ink having isobutyl methacrylate binder modified with maleic rosin and polyisoprene.
  • the protective coating layer 40 has a preferred formulation shown in Table II. It is composed essentially of a film-forming, multiaromatic, acid-based polyester designated polymer (I) and a second reinforcing polymer (ii) which contains a bulky ring structure such as a polymerized rosin ester.
  • the reinforcing polymer (ii) desirably may constitute between about 20 to 50 weight percent and preferably about 20 weight percent of the dried protective layer (40).
  • the polymers (i) and (ii) should be soluble in the same or miscible solvents, such as toluene and methyethyl ketone.
  • the polymers (i) and (ii) may have a refractive index of about 1.5.
  • the multiaromatic acid-based polyester (Polymer (i)) is preferably composed of the reaction products of the polymer condensation products of polyester forming reactants of one or more glycols reacted with naphthalic, or phthalic acids.
  • a preferred polyester polymer (i) is a linear multiaromatic acid-based polyester such as that available under the trademark VITEL PE200 or VITEL PE222 from Goodyear Company of Akron, OH.
  • the polyesters sold under the above VITEL trademark are aromatic acid-based polyesters having yellow, amorphous granules of Acid Number from 1 to 10, preferably 1 to 4, a Shore Durometer Hardness of about 75 to 80D, a specific gravity of about 1.25, and a ring and ball softening point of about 150 to 170°C.
  • a preferred reinforcing polyester polymer (ii) is a rosin ester formed typically by reaction of polyhydric alcohols, maleic anhydride or phenol aldehyde and rosin acids such as abietic and pimeric acids.
  • the rosin ester, (Polymer (ii)) is preferably composed of methyl abietate, methyl hydroabietate, glyceryl hydroabietate, or ester gum.
  • a preferred reinforcing polymer (ii) of this type is sold under the trademark NEOLYN 23-75T from Hercules Chemical Company of Wilmington, Delaware.
  • a preferred protective coating layer 40 is formed of a polyester solution having the typical preferred composition set forth in Table II.
  • the polyester resinous solution is prepared by admixing the constituents in the proportions set forth in Table II utilizing conventional mixing techniques.
  • the polyester resinous solution is coated onto ink layer 30 by conventional printing methods such as by gravure, silk screen offset, or flexographic methods.
  • the gravure method is preferred because better process print and sharper coloring can be realized by this printing method as well as better economy and color consistency with long runs.
  • the dried protective coating layer 40 has a basis weight preferably between about 0.23-1.4 kg (0.5 to 3 Ibs.)/ream (279 m 2 (3000 sq. ft.) per ream).
  • the same preferred formulation above-described and as shown in Table II for the dried protective coating layer 40 may be used as an optional barrier layer 25 between ink layer 30 and the resinous coating layer 20.
  • the method of preparing the barrier layer may also be the same as above-described for preparing the protective coating 40 by utilizing the same preferred polyester resinous solution formulation illustrated in Table II. If a barrier coating is used, the dried barrier layer between ink layer 30 and resinous coating 20 typically has a basis weight of between about 0.23­1.4 kg (0.5 to 3 Ibs)/ream. Inclusion of a barrier coating is optional, but its use further protects ink layer 30 from having moisture vapor, oxygen, and grease absorbed to it through resinous coating 20.
  • the transfer pad is preferably composed of silicone rubber. It has been found to be advantageous to provide the silicon rubber pad with a smooth surface and a convex curvature facing transfer substrate 7 so that the transfer substrate 7 has a smooth, glossy surface after it has been transferred to the article.
  • Any commercially available room temperature or heat curable silicone rubber may be suitable to make the pad.
  • the pad may be formed by casting room temperature vulcanisable silicone rubber with a suitable curing agent in proportion typically of 10 parts by weight silicon rubber to 1 part by weight curing agent.
  • a suitable room temperature vulcanizable silicone rubber can be purchased under the tradename RTV 700, and the curing agent under the tradename BETA 5, both available from General Electric Company of Pittsfield, MA.
  • the cast silicone rubber pad product preferably has a Shore A hardness of about 4 to 35.
  • a support 10 in the form of paper web carrying a multiplicity of transfer substrates 7 aligned in single rows were passed under a silicone rubber transfer pad 50 having a smooth surface.
  • An automatic conveyer was used to pass the transfer substrates 7 to and under the transfer pad 50.
  • the paper web was composed of Kraft-type paper having a basis weight of between about 9-18 kg (20 to 40 pounds) per ream and the substrate 7 was made in accordance wihh the specification set forth in Example II.
  • the support 10 was heated to a temperature of about 177°C (350°F). At this temperature level the protective coating 40 became tacky and the resinous coating softened and began to melt.
  • the silicone transfer rubber pad 50 was heated to between about 93-121 0 C (200 to 250°F). As each heated substrate 7 in turn passed under hot transfer pad 50, the smooth surface of the transfer pad made pressure contact with protective coating 40 in an automatic operation. As transfer pad 50 was withdrawn, the resinous coating 20 partially separated from support 10, thus releasing substrate 7 from support 10 exposing coating 20 to the environment, with coating 40 adhered to the transfer pad.
  • the transfer pad 50 and adhering substrate 7 was then pressed onto the surface of an article 60 which was conveyed to the vicinity of the transfer pad.
  • Article 60 was comprised of a polyethylene, and had compound curves and irregular surfaces.
  • the time interval between the moment of release of substrate 7 from support 10 to the moment of contact of substrate 7 with the article was about one second.
  • the paper web (support 10) which was affixed with the remaining substrates 7 was conveyed automatically under transfer pad 50. As each substrate 7 in turn passed under the transfer pad, the above-described sequence was repeated to transpose a substrate 7 from the web to another article. The process was repeated automatically until all the articles on the assembly line were imprinted with a substrate 7.
  • a web of support 10 composed of Kraft-type paper sheet having a basis weight of about 11.8-18.1 kg (26 to 40 Ibs)/ream was fed through a gravure printer.
  • the resinous coating (20) is formed over predesignated portions on the paper sheet by utilizing conventional gravure printing to apply the polyamide resinous solution to the paper sheet.
  • the polyamide resinous solution may be prepared in accordance with the formulation set forth in Table I as described in the foregoing. To facilitate the application of the resinous solution, it may be diluted further with solvent as desired, preferably so that its viscosity is about 25 sec. as measured with a #4 Ford cup. As the paper web was passed through the gravure printer, a coating of the polyamide resinous solution was uniformly applied to cover predesignated portions on a side of the paper sheet.
  • the coated paper was then passed through a conventional convective coater dryer wherein the coating is dried at about 93-121 0 C (200° to 250°F) evaporating the solvents and producing a dried resinous coating layer (20) having a composition typically as shown in Table I and a basis weight of between about 0.68­6.8 kg (1.5 to 15 Ibs.)/ream (2.79 m 2 (3000 sq. ft.)/ream).
  • ink layer 30 composed of isobutylmethacrylate ink modified with maleic rosin and polyisoprene was applied over the dried resinous coating.
  • a single ink color or multicolored inks including halftones may be applied to produce an imprint design or any number of colors.
  • the substrate overcoated with ink layer 30 was further passed sequentially to conventional convective drying carried out at about 93-121 0 C (200 to 250°F) to dry the ink.
  • the dried substrate was then again passed through a gravure printer wherein the polyester resinous solution was applied over ink layer 30.
  • a polyester resinous solution was then applied in accordance with the formulation set forth in Table II as described in the foregoing. However, to facilitate application of this solution by gravure imprinting, the solution was first further diluted with solvent to yield a viscosity of about 20 seconds as measured with a #4 Ford cup.
  • the substrate overcoated with the polyester resinous solution was dried in conventional convective coater dryers operating at about 93-121 * C (200°F to 250°F) until the polyester resinous solution dried to form a dried protective layer 40 having the typical preferred composition shown in Table II, and a basis weight of between about 0.23-1.4 kg (0.5 to 3 lbs.)/ream.
  • a label-bearing web was produced as in Example II with the following modification.
  • the substrate overcoated with dried resinous coating 20 was passed through a gravure printer in order to apply a barrier coating 25 over ink layer 30.
  • the barrier coating 25 was composed of the area polyester resinous solution shown in Table II.
  • the barrier coating was dried in conventional convective coater driers at about 93-121 0 C (200°F to 250°F) forming a barrier having typically the same composition as that of bhe dried protective layer 40 set forth in Table II and a basis weight between about 0.23-1.4 kg (0.5 to 3 lbs.)/ream.
  • the substrate 7 was formed of a coating layer 20, optional barrier layer 25, ink layer 30 and dried protective coating 40.
  • rows of individual substrates 7 may be printed onto support substrate 10 in mass production automated fashion.
  • Example 11 The process of the invention was carried out in accordance with Example 11 and the laminate 5 and substrate 7 were manufactured as set forth in Example II except that ink layer 30 was not overcoated with protective coating 40. Instead substrate 7 was formed as illustrated in Figures 4 or 5 with the free surface of ink layer 30 exposed.
  • transfer pad 50 was pressed onto substrate 7 the pad made direct contact with the exposed surface of ink layer 30 and after substrate 7 was transferred to article 60 the free surface of ink layer 30 was left exposed to the environment.
  • ink layer 30 was formed by employing an ink formed of conventional pigment, a binder solvent, and a binder composed of a film-forming isobutyl methacrylate ink modified with maleic rosin and polyisoprene.
  • the isobutyl methacrylate was present in the binder in an amount between about 60 to 80 percent by weight of the binder, the maleic rosin between about 15 to 25 percent by weight and the polyisoprene between about 5 to 15 percent by weight of the binder.
  • a typical preferred binder used in forming ink layer 30 was composed of 70 parts by weight isobutyl methacrylate modified with 20 parts by weight maleic rosin and 10 parts by weight polyisoprene.
  • the ink layer 30 was coated onto resinous coating 20 or alternatively onto barrier layer 25 and dried in the manner set forth in Example II to form the substrate 7 illustrated in Figures 4 and 5 respectively.
  • the dried ink layer 30 had a basis weight of between about 0.23-0.9 kg (0.5 to 2 Ibs.)/ream.
  • the ink layer 30 in the embodiment exhibited the required adhesive characteristics to permit transfer of substrate 7 to transfer pad 50 and thence to article 60 when the process of the invention was carried out as set forth in Example I.
  • the ink design in ink layer 30 was left indelibly imprinted on article 60.
  • Ink layer 30 exhibited abrasion and corrosion resisting properties sufficient to permit a variety of applications, particularly where article 60 contains chemically inactive and nontoxic components and where article 60 is not intended to come into contact frequently with highly abrasive materials.
  • transfer substrate 7 is removed from substrate 10, transferred to heated pad 50 and then to the desired article within the context of an automated process in the foregoing description, it should be appreciated that other variations including manual transfer of substrate 7 are also within the scope of the present invention.
  • the preferred substrate compositions disclosed herein admit suitable substitutions for the various components, within the scope of the adhesive/release laminate and the process for transferring this laminate to articles.
  • the quantity of a ream represents 500 sheets.

Landscapes

  • Decoration By Transfer Pictures (AREA)
  • Laminated Bodies (AREA)

Claims (7)

1. Verfahren zum Übertragen eines Dekorlaminats (5) von einem Trägermaterial (10) auf einen Gegenstand (60), bei dem das Verbundmaterial eine harzartige Klebe/Ablöseschicht (20) in Kontakt mit dem Trägermaterial, wobei keine Ablöseschicht auf Wachsbasis zwischen der Klebe/Ablöseschicht (20) und dem Trägermaterial vorhanden ist, und eine Dekorschicht (30:40) aufweist; wobei das Verfahren umfaßt: das Erwärmen des Laminats auf eine erste Temperatur oberhalb des Schmelzpunktes der Kleber-Ablöseschicht (20) dadurch, daß dem Trägermaterial Wärme zugeführt wird; das Erwärmen der Oberfläche eines elastomeren Elements (50) auf eine zweite unterhalb der ersten liegende Temperatur; die Herstellung eines Druckkontaktes zwischen dem Laminat (5) und dem erwärmten elastomeren Element (50), so daß das Laminat an dem elastomeren Element haften bleibt und beim Zurückziehen des elastomeren Elements von dem Trägermaterial (10) abgetrennt wird; das Pressen des Laminats (5) gegen den Gegenstand (60), um die Klebe/Ablöseschicht (20) damit zu verbinden; und das Entfernen des elastomeren Elements (50) von dem Gegenstand, wonach das Laminat an dem Gegenstand (60) haften bleibt; daudrch gekennzeichnet, daß die Klebe/Ablöseschicht (20) ein Polyamid enthält, welches das Polymerisationsprodukt eines Diamins mit einer dimerisierten Fettsäure ist.
2. Verfahren nach Anspruch 1 oder 2, bei dem das Übertragungslaminat (5) ohne nachfolgendes Brennen des Laminats dauerhaft an dem Gegenstand (60) haften bleibt.
3. Verfahren nach Anspruch 1 oder 2, bei dem die erste Temperatur in dem Bereich von 166°C-216°C (330°F-420°F) liegt.
4. Verfahren nach einem der vorhergehenden Ansprüche, in dem die zweite Temperatur in dem Bereich von 66°C-149°C (150°F-300°F) liegt.
5. Verfahren nach einem der Ansprüche 1 bis 4, bei dem das Laminat (5) weiterhin eine Schutzschicht (40) über der Dekorschicht (30:40) aufweist.
6. Verfahren nach einem der-Ansprüche 1 bis 5, bei dem das Laminat (5) weitherin eine Sperrschicht (25) zwischen der Klebe/Ablöseschicht (20) und der Dekorschicht (30:40) aufweist.
7. Verfahren nach einem der Ansprüche 1 bis 6, bei dem das elastomere Element (50) Silikongummi mit einer platten konvexen Oberfläche enthält.
EP19830901669 1983-03-10 1983-04-12 Stempeldekor mittels hitzeübertragung und dessen substrate Expired EP0138809B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT83901669T ATE36280T1 (de) 1983-03-10 1983-04-12 Stempeldekor mittels hitzeuebertragung und dessen substrate.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US47390683A 1983-03-10 1983-03-10
US473906 1983-03-10

Publications (3)

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EP0138809A1 EP0138809A1 (de) 1985-05-02
EP0138809A4 EP0138809A4 (de) 1985-07-30
EP0138809B1 true EP0138809B1 (de) 1988-08-10

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EP19830901669 Expired EP0138809B1 (de) 1983-03-10 1983-04-12 Stempeldekor mittels hitzeübertragung und dessen substrate

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EP (1) EP0138809B1 (de)
JP (1) JPS60500854A (de)
CA (1) CA1222684A (de)
DE (1) DE3377634D1 (de)
WO (1) WO1984003473A1 (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1319862C (en) * 1986-01-14 1993-07-06 Bruce E. Johnson Composite useful for paint transfer and method of use and preparation thereof
GB8610692D0 (en) * 1986-05-01 1986-06-04 Brittains Tr Ltd Transfer
US5215826A (en) * 1990-09-25 1993-06-01 Rexham Industries Corp. Surfacing film with thermoformable carrier layer
DE102017104658B4 (de) * 2017-03-06 2022-06-23 Leonhard Kurz Stiftung & Co. Kg Verfahren zur Herstellung eines Decals und ein Decal sowie ein Verfahren zum Dekorieren von Oberflächen von Gegenständen

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2268262A (en) * 1941-12-30 Configurable platen fob label
NL132089C (de) * 1900-01-01
US3616176A (en) * 1967-11-07 1971-10-26 Gen Mills Inc Polyamide decal
US3887420A (en) * 1971-04-30 1975-06-03 Pictorial Prod Inc Offset transfer of decalcomanias
US4288479A (en) * 1973-09-24 1981-09-08 Design Cote Corp. Radiation curable release coatings
DK153348C (da) * 1974-06-03 1988-11-14 Dennison Mfg Co Overfoeringsetiket og fremgangsmaade til fremstilling deraf
FR2300841A1 (fr) * 1975-02-13 1976-09-10 Noridem Etudes Procede Supports provisoires et leur procede de fabrication
US4016021A (en) * 1976-03-29 1977-04-05 Fleur Lee Heat sealing unit and method of making same
US4068033A (en) * 1976-11-17 1978-01-10 Commercial Decal, Inc. Heat-releasable decalcomanias and adhesive composition therefor
US4187223A (en) * 1976-12-29 1980-02-05 Sterling Drug Inc. 3-[4-(Disubstituted-amino)phenyl]-3-(diphenylamino)phthalides
JPS5465614A (en) * 1977-11-01 1979-05-26 Toppan Printing Co Ltd Copying sheet for polyamide
US4303717A (en) * 1979-08-23 1981-12-01 Commercial Decal, Inc. Heat release layer for decalcomanias
US4373984A (en) * 1980-07-16 1983-02-15 Voorwood Company Machine for applying transfer foil to a shaped edge of a substrate
US4597815A (en) * 1980-11-29 1986-07-01 Nissha Printing Co., Ltd. Transfer printing

Also Published As

Publication number Publication date
DE3377634D1 (en) 1988-09-15
EP0138809A1 (de) 1985-05-02
WO1984003473A1 (en) 1984-09-13
CA1222684A (en) 1987-06-09
JPS60500854A (ja) 1985-06-06
EP0138809A4 (de) 1985-07-30

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