Background of the Invention In recent years, a significant industry has developed which involves the application of customer-selected designs, messages, illustrations, and the like (referred to collectively hereinafter as "customer-selected graphics") on articles of clothing, such as T-shirts, sweat shirts, and the like. These customer-selected graphics typically are commercially available products tailored for a specific end-use and are printed on a release or transfer paper. The graphics are transferred to the article of clothing by means of heat and pressure, after which the release or transfer paper is removed.

Heat transfer papers having an enhanced receptivity for images made by wax-based crayons, thermal printer ribbons, and impact ribbon or dot-matrix printers, are well known in the art. Typically, a heat transfer sheet comprises a cellulosic base sheet and an image- receptive coating on a surface of the base sheet. The image-receptive coating usually contains one or more film-forming polymeric binders, as well as, other additives to improve the transferability and printability of the coating. Other heat transfer sheets comprise a cellulosic base sheet and an image-receptive coating, wherein the image-receptive coating is formed by melt extrusion or by laminating a film to the base sheet. The surface of the coating or film may then be

roughened by, for example, passing the coated base sheet through an embossing roll.

Much effort has been directed at generally improving the transferability of an image-bearing laminate (coating) to a substrate.

For example, an improved cold-peelable heat transfer material has been described in U. S. Patent No. 5,798,179, which allows removal of the base sheet immediately after transfer of the image-bearing laminate ("hot peelable heat transfer material") or some time thereafter when the laminate has cooled ("cold peelable heat transfer material"). Moreover, additional effort has been directed to improving the crack resistance and washability of the transferred laminate. The transferred laminate must be able to withstand multiple wash cycles and normal"wear and tear"without cracking or fading.

Various techniques have been used in an attempt to improve the overall quality of the transferred laminate and the article of clothing containing the same. For example, plasticizers and coating additives have been added to coatings of heat transfer materials to improve the crack resistance and washability of image-bearing laminates on articles of clothing. However, cracking and fading of the transferred image-bearing coating continues to be a problem in the art of heat transfer coatings.

Conventional heat transfer materials result in less than desirable finished products due to the relatively large thickness of the transfer coating. In conventional"hot peel"heat transfer processes, a relatively thick transfer coating layer is required to avoid quality problems, such as splitting of the transfer coating while the base sheet is removed. In conventional"cold peel"heat transfer processes, all of the transfer coating is released from the base sheet, forming a relatively thick coating. Typically, in these processes the transfer coating thickness is at least 40 grams per square meter (gsm). The relatively thick coatings fill the gaps within and between adjacent yarns of the coated fabric, forming bridges over the yarn gaps. The bridges tend to crack when the fabric is washed, resulting in a very poor appearance.

Furthermore, the thick transfer coating tends to become sticky when exposed to hot air, such as found in a clothes dryer, such that garments stick together if dried in a hot clothes dryer.

In addition to the problems of cracking and fading of the transferred image-bearing coating, the breathability of the coated article of clothing continues to be a problem using conventional heat transfer coatings. Conventional heat transfer coatings, whether

applied using a hot-peelable heat transfer material or a cold-peelable heat transfer material, require a minimal coating thickness in order to produce a continuous image-bearing coating. This results in a finished article of clothing having negligible breathability.

What is needed in the art is a heat transfer material, which substantially resists cracking while maintaining or enhancing the breathability of the coating. What is also needed in the art is a heat transfer material having a heat fusible coating thereon, wherein the heat fusible coating enables the production of a finished, image- bearing, article of clothing having breathability.

Summary of the Invention The present invention addresses some of the difficulties and problems discussed above by the discovery of a heat transfer material having a unique structure, which enables the transfer of a continuous, image-bearing coating onto an article of clothing, wherein the transfer coating thickness is less than conventional transfer coatings. The heat transfer material of the present invention may be applied, using a hot or cold peelable method, without the processability and quality problems associated with conventional heat transfer materials.

The heat transfer material of the present invention contains an interior meltable layer, a surface meltable layer, and a release coating layer. The release coating layer separates the two meltable layers.

During application with heat and pressure, the interior meltable layer, release coating layer, and surface meltable layer penetrate into the yarn interstices, or other undulations, of a given substrate to be coated.

However, only the surface meltable layer transfers to the substrate. The resulting transfer coating has a coating thickness less than conventional coatings, which provides improved breathability of the coated substrate.

The present invention is also directed to a method of making a printable heat transfer material having the above described structure. The method includes the steps of applying a release coating to an interior meltable layer and applying a surface meltable layer to the release coating layer.

The present invention is further directed to a method of transfer coating using the above described printable heat transfer material. The method includes the steps of applying heat and pressure to the heat transfer material and removing the interior meltable layer and release layer from the coated substrate.

These and other features and advantages of the present invention will become apparent after a review of the following detailed description of the disclosed embodiments and the appended claims.

Brief Description of the Drawings Fig. 1 is a fragmentary sectional view of a first embodiment of a printable heat transfer material of the present invention.

Fig. 2 is a fragmentary sectional view of a second embodiment of a printable heat transfer material of the present invention.

Detailed Description of the Invention The present invention is directed to a unique heat transfer material for use in transferring an image-bearing coating onto a substrate, such as an article of clothing. The heat transfer material of the present invention may be used in both hot and cold peel transfer processes, resulting in an image-bearing coating having superior crack resistance, washability, and breathability compared to conventional image-bearing coatings. The heat transfer material of the present invention produces superior results due to its unique multi-layer structure.

The heat transfer material of the present invention comprises at least two meltable layers separated by a release coating layer. The first meltable layer, designated an interior meltable layer (or base coating), along with the release layer, provide a"penetrating effect"to the heat transfer sheet, which forces the second meltable layer, designated the surface meltable layer (or print coating), into the interstices of a given substrate to be coated, such as a T-shirt. In addition to the layers above, the heat transfer material of the present invention may include one or more of the following layers: a base substrate, a sub-coating layer, and a top coating layer. Each of the individual layers of the heat transfer material, when present, provides a desirable property to the overall heat transfer sheet.

The heat transfer material of the present invention may comprise various layers as discussed above. In one embodiment of the present invention, shown in Fig. 1, the heat transfer material 10 comprises a first meltable layer (interior meltable layer) 11; a release layer 12, provided on a surface 13 of first meltable layer 11; and a second meltable layer (surface meltable layer or print layer) 14, provided on a surface 15 of release layer 12. In a further embodiment

of the present invention, shown in Fig. 2, the heat transfer material 20 comprises a base layer 21; a first meltable layer (interior meltable layer) 23, provided on a surface 22 of base layer 21; a release layer 25, provided on a surface 24 of first meltable layer 23; a sub-coating layer 27, provided on a surface 26 of release layer 25; a second meltable layer (surface meltable layer) 29, provided on a surface 28 of sub-coating layer 27; and a top coating layer 31, provided on a surface 30 of second meltable layer 29. Each of the above-mentioned individual layers of the heat transfer materials of the present invention are described below.

The interior meltable layer of the heat transfer material of the present invention may comprise any material capable of melting and conforming to the surface of a substrate to be coated. Desirably, the interior meltable layer has a melt flow index of less than about 500 and a melting temperature and/or a softening temperature of less than about 400°F. As used herein,"melting temperature"and"softening temperature"are used to refer to the temperature at which the meltable layer melts and/or flows under conditions of shear. More desirably, the interior meltable layer has a melt flow index of from about 0.5 to about 100, and a softening temperature of from about 150°F to about 300°F. Even more desirably, the interior meltable layer has a melt flow index of from about 2 to about 50, and a softening temperature of from about 200°F to about 250°F.

Since the interior meltable layer is not transferred to the coated substrate, the composition and thickness of the interior meltable layer may vary considerably, as long as the layer is meltable and conformable. The interior meltable layer may comprise one or more thermoplastic polymers including, but not limited to, polyolefins and ethylene-containing homopolymers and copolymers. In addition to the thermoplastic polymer (s), other materials may be added to the interior meltable layer to provide improved melt flow properties, such as plasticizers in solid or liquid form. Further, other materials may be added to improve the coating characteristics in liquid carriers including, but not limited to, surfactants and viscosity modifiers. Desirably, the interior meltable layer comprises up to about 5 wt% of one or more additives, based on the total weight of the dry interior meltable layer.

Suitable surfactants include, but are not limited to, an ethoxylated alcohol surfactant available from Union Carbide (Danbury, CT) under the tradename TERGITOL 15-S40, and a nonionic surfactant available

from Union Carbide under the tradename TRITON X100. Suitable viscosity modifiers include, but are not limited to, polyethylene oxide available from Union Carbide under the tradename POLYOX N60K and methylcellulose.

In an alternative embodiment of the present invention, the interior meltable layer may be in the form of a melt-extruded film.

The extruded film may comprise one or more of the above-described materials having the desired meltability and conformability properties.

In one embodiment of the present invention, the interior meltable layer comprises an extruded film of ELVAX 3200, a wax modified ethylene-vinyl acetate copolymer having a melt index of 30 available from DuPont (Wilmington, DE); an extruded film of ENGAGE 8200, a metallocene catalyzed, highly branched polyethylene having a melt index of 5 available from Dow Chemical Company (Midland, MI); or a combination of the ELVAX 3200 or ENGAGE 8200 material with one or more co-extruded layers. In a further embodiment of the present invention, the interior meltable layer comprises a co-extruded film having a layer of ELVAX 3200 and a layer of SURLYN 1702, an ethylene-methacrylic acid ionomer having a melt index of 15, also available from DuPont.

The interior meltable layer of the heat transfer material of the present invention may have a layer thickness, which varies considerably depending upon a number of factors including, but not limited to, the substrate to be coated, the press temperature, and the press time. Desirably, the interior meltable layer has a thickness of less than about 5 mil. (0.13 mm). More desirably, the interior meltable layer has a thickness of from about 0.5 mil. to about 4.0 mil. Even more desirably, the interior meltable layer has a thickness of from about 1.0 mil. to about 2.0 mil.

In addition to the interior meltable layer, the heat transfer material of the present invention comprises a release coating layer.

The release coating layer separates the transferable material of the heat transfer sheet from the non-transferable material of the heat transfer sheet. Like the interior meltable layer, the release coating layer does not transfer to a coated substrate. Consequently, the release coating layer may comprise any material having release characteristics, which is also conformable when heated. Desirably, the release coating layer does not melt or become tacky when heated, and provides release of an image-bearing coating during a hot or cold peelable transfer

process. The release coating layer may be adjacent to a surface of the interior meltable layer or may be separated from the interior meltable layer by one or more layers.

A number of release coating layers are known to those of ordinary skill in the art, any of which may be used in the present invention. Typically, the release coating layer comprises a cross-linked polymer having essentially no tack at transfer temperatures (e. g.

177°C) and a glass transition temperature of at least about 0°C. As used herein, the phrase"having essentially no tack at transfer temperatures"means that the release coating layer does not stick to an overlaying layer to an extent sufficient to adversely affect the quality of the transferred image. Suitable polymers include, but are not limited to, silicone-containing polymers, acrylic polymers and poly (vinyl acetate). Further, other materials having a low surface energy, such as polysiloxanes and fluorocarbon polymers, may be used in the release coating layer, particularly in cold peel applications.

Desirably, the release coating layer comprises a cross-linked silicone- containing polymer or a cross-linked acrylic polymer. Suitable silicone- containing polymers include, but are not limited to, SYL-OFF 7362, a silicone-containing polymer available from Dow Corning Corporation (Midland, MI). Suitable acrylic polymers include, but are not limited to, HYCAR 26672, an acrylic latex available from B. F. Goodrich, Cleveland, OH; MICHEM Prime 4983, an ethylene-acrylic acid copolymer dispersion available from Michelman Chemical Company, Cincinnati, OH; HYCAR 26684, an acrylic latex also available from B. F. Goodrich, Cleveland, OH; and RHOPLEX SP 100, an acrylic latex available from Rohm & Haas, Philadelphia, PA.

The release coating layer may further contain additives including, but not limited to, a cross-linking agent, a release-modifying additive, a curing agent, a surfactant and a viscosity-modifying agent.

Suitable cross-linking agents include, but are not limited to, XAMA7, an aziridine cross-linker available from B. F. Goodrich. Suitable release- modifying additives include, but are not limited to, SYL-OFF 7210, a release modifier available from Dow Corning Corporation. Suitable curing agents include, but are not limited to, SYL-OFF 7367, a curing agent available from Dow Corning Corporation. Suitable surfactants include, but are not limited to, TERGITOL 15-S40, available from Union Carbide; TRITON X100, available from Union Carbide; and Silicone Surfactant 190, available from Dow Corning Corporation. In

addition to acting as a surfactant, Silicone Surfactant 190 also functions as a release modifier, providing improved release characteristics, particularly in cold peel applications.

The release coating layer may have a layer thickness, which varies considerably depending upon a number of factors including, but not limited to, the substrate to be coated, the thickness of the interior meltable layer, the press temperature, and the press time. Desirably, the release coating layer has a thickness, which does not restrict the flow of the interior meltable layer and, which provides a continuous physical barrier between the transferable material and the non- transferable material of the heat transfer sheet. Typically, the release coating layer has a thickness of less than about 1 mil. (26 microns).

More desirably, the release coating layer has a thickness of from about 0.05 mil. to about 0.5 mil. Even more desirably, the release coating layer has a thickness of from about 0.08 mil. to about 0.33 mil.

The thickness of the release coating layer may also be described in term of a basis weight. Desirably, the release coating layer has a basis weight of less than about 6 lb./144 yd2 (22.5 gsm). More desirably, the release coating layer has a basis weight of from about 3.0 lb./144 yd2 (11.3 gsm) to about 0.3 lb./144 yd2 (1.1 gsm). Even more desirably, the release coating layer has a basis weight of from about 2.0 lb./144 yd2 (7.5 gsm) to about 0.5 lb./144 yd2 (1.9 gsm).

The heat transfer material of the present invention further comprises a surface meltable (or print coating) layer. Like the interior meltable layer, the surface meltable layer is capable of melting and conforming to the surface of a substrate to be coated. In addition, the surface meltable layer provides a print surface for the heat transfer sheet and is formulated to minimize feathering of a printed image and bleeding or loss of the image when the transferred image is exposed to water. The surface meltable layer is adapted to be printable by any method of printing including, but not limited to, ink jet printing, laser color copying, offset printing or other imaging methods. In some embodiments of the present invention, the surface meltable layer is adapted to be printable by an ink jet printer. In other embodiments, the surface meltable layer is adapted to be printable by color laser copiers. In still other embodiments, the surface meltable layer is adapted to be printable by thermal ribbon printers. Further, the surface meltable layer is capable of adhering directly to a given

substrate, such as a T-shirt, or indirectly to the substrate via additional intermediate layers to insure good image washability.

Although the melt flow properties of the surface meltable layer are not critical to the present invention, it is desirable for the surface meltable layer to have a high melt flow index and a low softening point. Desirably, the surface meltable layer has a melt flow index of more than about 10, and a softening temperature of less than about 350°F. More desirably, the surface meltable layer has a melt flow index of from about 20 to about 20,000, and a softening temperature of from about 150°F to about 300°F. Even more desirably, the surface meltable layer has a melt flow index of from about 30 to about 10,000, and a softening temperature of from about 200°F to about 250°F.

The surface meltable layer of the heat transfer sheet of the present invention may include one or more components including, but not limited to, particulate thermoplastic materials, film-forming binders, a cationic polymer, a humectant, cyclohexane dimethanol dibenzoate, ink viscosity modifiers, weak acids, surfactants, a dispersent, a plasticizer, and a buffering agent. Each component of the surface meltable layer provides a particular feature to the printable layer.

The surface meltable layer may contain one or more thermoplastic particles. Desirably, the particles have a largest dimension of less than about 50 micrometers. More desirably, the particles have a largest dimension of less than about 20 micrometers.

Suitable powdered thermoplastic polymers include, but are not limited to, polyolefins, polyesters, polyamides, and ethylene-vinyl acetate copolymers. In one embodiment of the present invention, the surface meltable layer contains thermoplastic particles in the form of micronized high density polyethylene powder available from Micropowders, Inc., Scarsdale, NY under the tradenames MPP635VF and MPP635G; co-polyamide 6-12 particles having an average particle size of 10 microns available from Elf Atochem, Paris, France under the tradename ORGASOL 3501 EXDNAT 1; polyester powder available from Image Polymers Inc., Wilmington, MA under the tradename ALMACRYL P-501; or a combination thereof.

The surface meltable layer may also contain one or more film- forming binders. Desirably, the one or more film-forming binders are present in an amount of from about 10 to about 100 weight percent, based on the weight of the thermoplastic polymer. More desirably,

the amount of binder is from about 10 to about 50 weight percent.

Suitable binders include, but are not limited to, polyacrylates, polyethylenes, ethylene-acrylic acid copolymers, and ethylene-vinyl acetate copolymers. Desirably, the binders are heat-softenable at temperatures of less than or about 350°F. In one embodiment of the present invention, the surface meltable layer contains one or more film-forming binders in the form of an ethylene-acrylic acid copolymer dispersion available from Michelman, Chemical Company, Cincinnati, OH under the tradename MICHEM Prime 4983; a similar ethylene- acrylic acid copolymer dispersion also available from Michelman, Chemical Company, Cincinnati, OH under the tradename MICHEM (g Prime 4990; another ethylene-acrylic acid copolymer dispersion also available from Michelman, Chemical Company, Cincinnati, OH under the tradename MICHEM Prime 4990R; or an ethylene-vinyl acetate copolymer binder available from Air Products, Allentown, PA under the tradename AIRFLEX 540.

Further, the surface meltable layer may comprise a cationic polymer. In some instances, the cationic polymer enhances the retention of print on the surface of the surface meltable layer, particularly in the case of ink jet ink. Desirably, the cationic polymer is present in an amount from about 2 to about 20 weight percent, based on the weight of the thermoplastic polymer. Suitable cationic polymers include, but are not limited to, an amide-epichlorohydrin polymer, polyacrylamides with cationic functional groups, polyethyleneimines, and polydiallylamines. In one embodiment of the present invention, the surface meltable layer contains a cationic polymer in the form of a poly (N, N-dimethylethylamino methacrylate), quaternized with methyl chloride, available from Allied Colloids as a water solution under the tradename ALCOSTAT 567 or a poly (diallyldimethyl) ammonium chloride, also available from Allied Colloids as a water solution under the tradename ALCOSTAT 167.

The surface meltable layer of the heat transfer sheet may also contain one or more of the following: a surfactant and a viscosity modifier. Suitable surfactants include anionic, nonionic, or cationic surfactants. Desirably, the surfactant is a nonionic or cationic surfactant, such as those described above. Examples of anionic surfactants include, but are not limited to, linear and branched-chain sodium alkylbenzenesulfonates, linear and branched-chain alkyl sulfates, and linear and branched-chain alkyl ethoxy sulfates. Cationic

surfactants include, but are not limited to, tallow trimethylammonium chloride. More desirably, the surfactant is a nonionic surfactant.

Examples of nonionic surfactants include, but are not limited to, alkyl polyethoxylates, polyethoxylated alkylphenols, fatty acid ethanol amides, complex polymers of ethylene oxide, propylene oxide, and alcohols, and polysiloxane polyethers. Suitable viscosity modifiers include, but are not limited to, a polyethylene oxide thickener available from Union Carbide under the tradename POLYOX N60K; methylcellulose available from Dow Chemical under the tradename METHOCEL A-15; and hydroxypropylcellulose available from Hercules (Wilmington, DE) under the tradename KLUCEL L.

In one embodiment of the present invention, the surface meltable layer comprises one or more of the above-described components and cyclohexane dimethanol dibenzoate. The amount of cyclohexane dimethanol dibenzoate in the surface meltable layer may vary depending on the overall coating composition. Desirably, the amount of cyclohexane dimethanol dibenzoate in the surface meltable layer is up to about 50 wt% based on the total weight percent of the dry coating layer. More desirably, the amount of cyclohexane dimethanol dibenzoate in the surface meltable layer is from about 10 wt% to about 30 wt% based on the total weight percent of the dry coating layer. Even more desirably, the amount of cyclohexane dimethanol dibenzoate in the surface meltable layer is from about 15 wt% to about 25 wt% based on the total weight percent of the dry coating layer.

In a further embodiment of the present invention, the surface meltable layer comprises a dispersent and/or a buffering agent.

Suitable dispersents for the surface meltable layer of the present invention include, but are not limited to, KLUCEL L; TRITON X100; TAMOL (8) 731, available Rohm && Haas 15-S40, available from Union Carbide. Suitable buffering agents for the surface meltable layer of the present invention include, but are not limited to, sodium carbonate.

The surface meltable layer of the heat transfer material of the present invention may have a layer thickness, which varies considerably depending upon a number of factors including, but not limited to, the substrate to be coated, the thickness of the interior meltable layer, the thickness of the release coating layer, the press temperature, and the press time. Desirably, the surface meltable layer

has a thickness of less than about 2 mil. (52 microns). More desirably, the surface meltable layer has a thickness of from about 0.5 mil. to about 1.5 mil. Even more desirably, the surface meltable layer has a thickness of from about 0.7 mil. to about 1.5 mil.

The thickness of the surface meltable layer may also be described in term of a basis weight. Desirably, the surface meltable layer has a basis weight of less than about 12 lb./144 yd2 (48 gsm).

More desirably, the surface meltable layer has a basis weight of from about 8.0 lb./144 yd2 (30.2 gsm) to about 2.0 lb./144 yd2 (7.5 gsm).

Even more desirably, the surface meltable layer has a basis weight of from about 8.0 lb./144 yd (30.2 gsm) to about 3.0 lb./144 yd2 (11.2 gsm).

In addition to the layers described above, the heat transfer sheet of the present invention may comprise a base substrate. Suitable base substrates include, but are not limited to, cellulosic nonwoven webs and polymeric films. A number of suitable base substrates are disclosed in U. S. Patents Nos. 5,242,739; 5,501,902; and 5,798,179; the entirety of which are incorporated herein by reference. Desirably, the base substrate comprises paper. A number of different types of paper are suitable for the present invention including, but not limited to, common litho label paper, bond paper, and latex saturated papers.

The heat transfer material of the present invention may further comprise a sub-coating layer. The sub-coating layer may be positioned next to or separate from the surface meltable layer. Desirably, the sub- coating layer is directly above the release coating layer, so as to provide a desired amount of adhesion between the release coating layer and an overlaying layer, such as the surface meltable layer. The sub-coating layer provides an adequate amount of adhesion for manufacture, sheeting, handling, and printing of the heat transfer material, yet low enough adhesion for easy release after transfer. The sub-coating layer also provides protection to the surface meltable layer, which improves the washability of the transferred coating. A number of sub-coating layers are known to those of ordinary skill in the art, any of which may be used in the present invention. Suitable sub-coating layers for use in the present invention are disclosed in U. S.

Patent No. 5,798,179, the entirety of which is incorporated herein by reference.

In one embodiment of the present invention, the sub-coating layer of the heat transfer material comprises at least one film-forming

binder material. The sub-coating layer of the heat transfer material may further comprise one or more powdered thermoplastic polymers.

Suitable film-forming binder materials and powdered thermoplastic polymers include, but are not limited to, those described above.

Desirably, the film-forming binder material is ethylene-acrylic acid copolymer dispersion available from Michelman, Chemical Company, Cincinnati, OH under the tradename MICHEM Prime 4990 or an acrylic latex available from B. F. Goodrich, Cleveland, OH under the tradename HYCAR 26684. Desirably, the thermoplastic polymer particles are co-polyamide 6-12 particles having an average particle size of 10 microns available from Elf Atochem, Paris, France under the tradename ORGASOL 3501 EXDNAT 1; micronized high density polyethylene powder available from Micropowders, Inc., Scarsdale, NY under the tradename MPP635VF; polyester powder available from Image Polymers Inc., Wilmington, MA under the tradename ALMACRYL P-501; or a combination thereof. More desirably, the thermoplastic polymer particles are ORGASOL 3501 EXDNAT 1 particles. The sub-coating layer may include other additives such as those described above for the surface meltable layer.

The thickness of the sub-coating layer may vary considerably depending upon the desired properties of the image-bearing transfer coating. Desirably, the sub-coating layer has a basis weight of less than about 6 lb./144 yd (22.8 gsm). More desirably, the sub-coating layer has a basis weight of from about 5.0 lb./144 yd2 (18.9 gsm) to about 0.5 lb./144 yd2(1.9 gsm). Even more desirably, the sub-coating layer has a basis weight of from about 4.0 lb./144 yd2 (15.1 gsm) to about 1.0 lb./144 yd2 (3.8 gsm).

The heat transfer sheet of the present invention may further comprise a top coating layer to enhance absorption of ink jet inks and prevent feathering. The top coating layer may contain a wetting agent and an ink viscosity modifier. Desirably, the top coating layer comprises one or more cationic polymers. Suitable cationic polymers include, but are not limited to, poly (N, N-dimethylethylamino methacrylate), quarternized with methyl chloride, sold under the tradename, ALCOSTAT 567 from Allied Colloids. Other materials may be added to the top coating layer including, but not limited to, plasticizers, surfactants, and viscosity modifiers. Suitable viscosity modifiers include, but are not limited to, polyethylene oxide available

from Union Carbide under the tradename POLYOX N60K, as well as, methylcellulose or hydroxyethyl cellulose. In one embodiment of the present invention, the heat transfer sheet includes a top coating layer comprising a mixture of 2 parts by weight (pbw) of ALCOSTAT 567, 2 pbw of POLYOX N60K, and 1 pbw of KLUCEL L.

The thickness of the top coating layer may vary considerably depending upon a number of factors including, but not limited to, the desired properties of the image-bearing transfer coating, the type of print, and the printing means. Desirably, the top coating layer has a basis weight of less than about 2 lb./144 yd (7.5 gsm). More desirably, the top coating layer has a basis weight of from about 1.0 lb./144 yd2 (3. 8 gsm) to about 0.1 lb./144 yd2 (0.4 gsm). Even more desirably, the top coating layer has a basis weight of from about 0.75 lb./144 yd2 (2.8 gsm) to about 0.25 lb./144 yd2 (0.9 gsm).

The image-bearing coating of the heat transfer sheet, comprising one or more of the above-described coating layers, may be transferred to an article of clothing, or other porous substrate, by applying heat and pressure to the coating. Desirably, the image- bearing coating of the heat transfer sheet melts and penetrates into the interstices of the substrate, as opposed to merely coating the substrate surface. In order to penetrate into a fabric, the combined thickness of the sub-coating layer, surface meltable layer, and top coating layer, when present, is desirably greater than about 1.0 mil. More desirably, the combined thickness of the sub-coating layer, surface meltable layer, and top coating layer is about 1.5 to about 3 mils.

In the present invention, the first meltable layer also conforms to the surface of the fabric, or other substrate, which may have an irregular (not flat) surface. This further enhances the penetration of the second meltable layer into low areas of the material. However, since only the second meltable layer transfers, a minimal amount of polymer may be left on the surface of the fabric. Since the yarns of the fabric are free from excess polymer, which forms polymer bridges and fills the valleys between adjacent yarns, the fabric feel and stretch are much improved over conventionally transfer-coated fabrics.

The amount of polymer actually transferred to the fabric or substrate may be as little as about 10 grams per square meter (gsm), as opposed to conventional amounts in the range of about 50 gsm.

Desirably, the basis weight of the image-bearing coating is less than about 40 gsm. More desirably, the basis weight of the image-bearing

coating is less than about 30 gsm. Even more desirably, the basis weight of the image-bearing coating is less than about 20 gsm.

The present invention is also directed to a method of making a printable heat transfer material. The method comprises forming a first or interior meltable layer, applying a release coating layer onto the interior meltable layer, and applying a second or surface meltable coating onto the release coating layer. In one embodiment of the present invention, one or more of the above-described coating compositions are applied to the interior meltable layer by known coating techniques, such as by solution, roll, blade, and air-knife coating procedures. Each individual coating may be subsequently dried by any drying means known to those of ordinary skill in the art.

Suitable drying means include, but are not limited to, steam-heated drums, air impingement, radiant heating, or a combination thereof. In an alternative embodiment, one or more of the above-described layers may be extrusion coated onto the surface of the interior meltable layer or a coating thereon. Any extrusion coating techniques, well known to those of ordinary skill in the art, may be used in the present invention.

In one embodiment of the present invention, a corona discharge process may be used to enhance the adhesion between the interior meltable layer and the release coating, applied to the interior meltable layer. Corona discharge methods are well known in the art. Suitable apparatus for performing the corona discharge step include, but are not limited to, treaters available from Enercon Industries, Corporation, Menomonee Falls, WI. Desirably, the corona discharge step used in the present invention applies an amount of treatment to the interior meltable layer to produce a surface tension of greater than about 40 dynes. In some cases, the corona discharge step produces an interior meltable layer having a surface tension of from about 40 to 50 dynes.

It should be noted that a corona discharge treatment may be applied to other layers of the heat transfer sheet, although such treatments are not necessary.

If desired, any of the foregoing coating layers may contain other materials, such as processing aids, release agents, pigments, deglossing agents, antifoam agents, and the like. The use of these and similar materials is well known to those having ordinary skill in the art.

The present invention is further directed to a method of transfer coating a substrate using the above-described heat transfer material.

The method comprises applying a sufficient amount of heat and pressure to the heat transfer material to melt the interior meltable

layer and the surface meltable layer of the heat transfer material, and removing the interior meltable layer and release layer from the coated substrate. Any known heating means may be used in the present invention including, but not limited to, a household iron and a commercial heating press. Heating temperature and press time may vary depending on a number of factors including, but not limited to, heating means, heating temperature, pressure applied, heat transfer sheet materials, and substrate structure.

The heat transfer sheet of the present invention may be used in hot peelable transfer processes, as well as, cold peelable transfer processes. As used herein, the phrase"hot peelable transfer process" refers to a process wherein one or more meltable layers is still in a molten state when a non-transferable portion of a heat transfer sheet is removed. Such a process allows release of the heat transfer sheet via splitting of the meltable layer (s). As used herein, the phrase"cold peelable transfer process"refers to a process wherein a non- transferable portion of a heat transfer sheet is removed from a transferable portion of the heat transfer sheet after the heat transfer sheet has cooled below the softening temperature of the transferable portion.

The present invention is further described by the examples which follow. Such examples, however, are not to be construed as limiting in any way either the spirit or scope of the present invention.

In the examples, all parts are parts by weight unless stated otherwise.

EXAMPLES Multiple transfers were performed using a variety of heat transfer materials. Each heat transfer sheet contained one or more of the following layers: base substrate; internal meltable layer; release coating layer; surface meltable layer; sub-coating layer; and top coating layer. A detailed description of each layer follows.

The coatings free of suspended particulate, such as some of the silicone release coatings, were made to the desired composition and dried to remove any solvent. Coatings containing suspended particulate were prepared using water as the dispersing medium. Water and/or solvent, if present in the coating, was removed by a drying step after applying the coating. Typically, drying took place for a period of about two minutes in a forced air oven at a temperature ranging from about 80°C to 110°C. A lower temperature of about 80°C was used to dry the ink jet print coatings. However, it should be

noted that any drying step may be used to remove water from the coating as long as the drying step does not negatively impact the coating.

Coatings containing polymeric powders or plasticizers were dispersed by putting the coating through a colloid mill and/or Cowles mixer.

BaseSubstrats BP1 BP1 was a 20 lb. (20 lb./144 yd2) bond paper from Neenah Paper, Roswell, GA, (a subsidiary of Kimberly-Clark Corporation) designated Avon Brilliant Classic Crest. The basis weight was 75 gsm and the thickness was 4 mils.

BP2 BP2 was a 20 lb. (20 lb./144 yd2) paper impregnated with a saturant comprising 100 dry parts AIRVOLs 107 (polyvinyl alcohol from Air Products), 50 dry parts titanium dioxide, and 4 dry parts of a sizing agent, SUNSIZE'137 (stearated melamine resin from Sequa Chemical, Chester, SC). The mixture was applied at about 12.5% total solids content in water. The saturant pickup was 15 parts per 100 parts fiber weight.

BP3 BP3 was a 22.5 lb. (22.5 lb./144 yd) litho label paper having a clay print coating on the backside. The paper was available from Interlake Paper Company, Wisconsin Rapids, WI, under the tradename REPAP° 9365.

BP4 BP4 was a 13 lb. (13 lb./144 yd2) base paper impregnated with an acrylic saturant comprising HYCAR 26083, a soft acrylic latex (available from B. F. Goodrich, Cleveland, OH). The saturant pickup was 30 parts per 100 parts paper weight to yield a total weight of 16.9 lb./144 yd2.

BP5 BP5 was a 15.2 lb. (15.2 lb./144 yd2) base paper impregnated with an acrylic saturant comprising HYCAR 26083. A frontside of the

impregnated paper was coated with a 4.0 lb./144 yd2 coating comprising 100 parts of ULTRAWHTTE 90 clay (available from Englehard, Iselin, NJ) and 35 parts HYCAR 26084 acrylic latex (available from B. F. Goodrich, Cleveland, OH). A backside of the impregnated paper was coated with a 5.5 lb./144 yd2 coating comprising 100 parts ULTRAWHITE 90 clay and 24 parts RHOPLEX HA16 acrylic binder (available from Rohm & Haas Company, Philadelphia, PA).

BP6 BP6 was a 24 lb. (24 lb./144 yd2) Neenah Avon Brilliant Classic Crest calendered to a thickness of 4.5 mils, available from Neenah Paper.

BP7 BP7 was a 24 lb. (24 lb./144 yd2) Neenah Avon Brilliant Classic Crest calendered to a thickness of 3.5 mils.

Internal Meltable (Base Coating) Layers BC1 BC1 was a film comprising NUCREL 599, an ethylene- methacrylic acid co-polymer having a melt index of 500, available from Dupont. The film had a thickness of 1.8 mil.

BC2 BC2 was a film comprising a 50/50 blend of NUCREL 599 and BYNEL 1124, an ethylene-vinylacetate-acid co-polymer having a melt index of 30, available from DuPont. The film had a thickness of 1.8 mil.

BC3 BC3 was a co-extruded film comprising a layer of EL VAX 3200 (a wax modified EVA copolymer having a melt index of 30, available from DuPont) having a thickness of 1.2 mil., and a layer of SURLYN 1702 (an ethylene-methacrylic acid ionomer having a melt index of 15, also available from DuPont) having a thickness of 0.6 mil.

BC4 BC4 was an extruded film comprising ELVAX 3200 and having a thickness of 1.8 mil.

BC5 BC5 was an extruded film comprising ENGAGE 8200, a metallocene catalyzed, highly branched, polyethylene, available from Dow Chemical Company (Midland, MI). The film had a thickness of 1.8 mil and a melt flow index of 5.

Release Coating Layers All of the release coatings were applied to a substrate using a Meyer rod technique and dried in a forced air oven at about 225°F (107°C).

RC1 Release coating RC1 was a mixture of the following components: SANCOR 776 100 dry parts XAMA7 5 dry parts SANCOR 776 is a polyurethane emulsion available from B. F.

Goodrich, Cleveland, OH.

XAMA7 is an aziridine cross-linker available from B. F. Goodrich.

The ingredients were mixed and applied to provide a dry coating weight of 1.5 lb./144 yd2 or about 5.7 gsm.

RC2 Release coating RC2 was identical to RC1 except that the release coating was applied to provide a dry coating weight of 0.6 lb./144 yd2 or about 2.3 gsm.

Release coating RC3 was a mixture of the following components: SANCOR 815 100 dry parts

XAMA7 5 dry parts SANCOR 815 is a hard polyurethane emulsion available from B. F. Goodrich, Cleveland, OH.

The ingredients were mixed and applied to provide a dry coating weight of 0.6 lb./144 yd2 or about 2.3 gsm.

RC4 Release coating RC4 was a mixture of the following components: SYL-OFF 7362 100 dry parts SYL-OFF 7210 0.2 dry parts SOL-OFF 7367 0.3 dry parts SYL-OFF 7362 is a silicone polymer available from Dow Corning Corporation (Midland, MI).

SYL-OFF 7210 is a release modifier available from Dow Corning Corporation.

SYL-OFF 7367 is a curing agent available from Dow Corning Corporation.

The ingredients were dissolved in toluene at 16 wt% total solids content. The release coating was applied to provide a dry coating weight of 0.35 lb./144 yd2 or about 1.3 gsm.

RC5 Release coating RC5 was identical to RC4 except that the release coating was applied to provide a dry coating weight of 0.7 lb./144 yd2 or about 2.6 gsm.

RC6 Release coating RC6 was a mixture of the following components: SYL-OFF 7362 100 dry parts SYL-OFF 7210 18.8 dry parts

SYL-OFF 7367 0.9 dry parts The ingredients were dissolved in toluene at 16 wt% total solids content. The release coating was applied to provide a dry coating weight of 0.7 lb./144 yd2 or about 2.6 gsm.

RC7 Release coating RC7 was a mixture of the following components: SYL-OFF 7362 100 dry parts SYL-OFF 7210 31.2 dry parts SYL-OFF 7367 1.9 dry parts The ingredients were dissolved in toluene at 16 wt% total solids content. The release coating was applied to provide a dry coating weight of 0.35 lb./144 yd2 or about 1.3 gsm.

RC8 Release coating RC8 was identical to RC7 except that the release coating was applied to provide a dry coating weight of 0.7 lb./144 yd2 or about 2.6 gsm.

RC9 Release coating RC9 was identical to RC7 except that the release coating was applied to provide a dry coating weight of 1.0 lb./144 yd or about 3.8 gsm.

RC10 Release coating RC10 was a mixture of the following components: HYCAR 26672 100 dry parts CELITE 263 30 dry parts NOPCOTE C-104 25 dry parts Silicone Surfactant 190 10 dry parts XAMA7 10 dry parts TRITON X100 3 dry parts

ammonia 2 parts HYCAR 26672 is an acrylic latex available from B. F. Goodrich, Cleveland, OH.

CELITE 263 is diatomaceous earth (de-glosser) available from Hydrite Chemical Company, Milwaukee, WI.

NOPCOTE C-104 is a 50% solids emulsion of calcium stearate available from Henkel Corporation, Ambler, PA.

Silicone Surfactant 190 is a release agent available from Dow Corning.

TRITON X100 is a nonionic surfactant available from Union Carbide.

The ingredients were mixed to provide 33 wt% total dry solids content. The release coating was applied to provide a dry coating weight of 1.5 lb./144 yd2or about 5.7 gsm.

RC11 Release coating RC11 was identical to RC10 except that the CELITE 263 was not present. The release coating was applied to provide a dry coating weight of 0.3 lb./144 yd2 or about 1.1 gsm.

RC12 Release coating RC12 was identical to RC10 except that the CELITE# 263 and NOPCOTE# C-104 were not present. The release coating was applied to provide a dry coating weight of 1.0 lb./144 yd2 or about 3.8 gsm.

RC13 Release coating RC13 was a mixture of the following components: HYCAR 26672 dry parts Silicone Surfactant 190 5 dry parts XAMA7 10 dry parts TRITON X100 3 dry parts ammonia 1 part POLYOX N60K 1 part

POLYOX N60K is a polyethylene oxide thickener available from Union Carbide, Danbury, CT.

The ingredients were mixed to provide 33 wt% total dry solids content. The release coating was applied to provide a dry coating weight of 1.0 lb./144 yd2 or about 3.8 gsm.

RC14 Release coating RC14 was identical to RC13 except that the release coating was applied to provide a dry coating weight of 0.5 lb./144 yd2 or about 1.9 gsm.

RC15 Release coating RC15 was identical to RC13 except that the Silicone Surfactant 190 was not present. The release coating was applied to provide a dry coating weight of 1.0 lb./144 yd or about 3.8 gsm.

RC16 Release coating RC16 was a mixture of the following components: MICHEM Prime 4983 100 dry parts XAMA7 10 dry parts TRITON X100 3 dry parts ammonia 2 parts MICHEM Prime 4983 is an ethylene-acrylic acid copolymer dispersion available from Michelman, Chemical Company, Cincinnati, OH.

The ingredients were mixed to provide 33 wt% total dry solids content. The release coating was applied to provide a dry coating weight of 1.0 lb./144 yd2 or about 3.8 gsm.

RC17 Release coating RC17 was a mixture of the following components: HYCAR 26684 100 dry parts TRITON X100 10 dry parts ammonia 1 part HYCAR 26684 is an acrylic latex available from B. F. Goodrich, Cleveland, OH.

The ingredients were mixed with water to provide 25 wt% total solids content. The release coating was applied to provide a dry coating weight of 1.0 lb./144 yd2or about 3.8 gsm.

RC18 Release coating RC18 was identical to RC12 except that the release coating was applied to provide a dry coating weight of 0.6 lb./144 yd2or about 2.3 gsm.

RC19 Release coating RC19 was a mixture of the following components: Q2-5211 0.2 dry parts RHOPLEX SP-100 200 dry parts CARBOWAX 8000 S. S. 20 dry parts Silicone Surfactant 190 4 dry parts XAMA7 10 dry parts ammonia 1.1 parts Q2-5211 is a surfactant available from Dow Corning, Midland, MI.

RHOPLEX SP-100 is an acrylic latex available from Rohm & Haas, Philadelphia, PA.

CARBOWAX 8000 is a polyethylene oxide available from Union Carbide, Danbury, CT.

The ingredients were mixed to provide 27.0 wt% total dry solids content. The pH was adjusted to within a range of 9 to 10. The XAMA7 was added to the mixture just prior to the coating process.

The release coating was applied to provide a dry coating weight of 2.0 lb./144 yd2or about 7.5 gsm.

Print Coating (Surface Meltable) Layers-Thermal Wax Ribbon Printers The following surface meltable coatings were used with Thermal Wax Ribbon printers. Each coating was applied using a Meyer rod technique and dried in a forced air oven at about 200°F (93°C). The particular Meyer rod used for a given coating (i. e., the Meyer rod number, such as number 6) was selected according to the desired basis weight of the final coating.

PCT1 Surface meltable coating PCT1 was a mixture of the following components: MPP635VF micropowder 100 dry parts TRITON X100 3 dry parts MICHEM Prime 4983 50 dry parts MPP635VF micropowder is a micronized high density polyethylene powder available from Micropowders, Inc., Scarsdale, NY, having an average particle size of 6 microns.

The mixture was dispersed in a Colloid mill. The total solids content was 37 wt% total dry solids in water. The surface meltable coating was applied to provide a dry coating weight of 2.0 lb./144 yd2 or about 7.5 gsm.

PCT2 Surface meltable coating PCT2 was identical to PCT1 except that the surface meltable coating was applied to provide a dry coating weight of 3.0 lb./144 yd2 or about 11.3 gsm.

PCT3 Surface meltable coating PCT3 was identical to PCT1 except that the surface meltable coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.1 gsm.

PCT4 Surface meltable coating PCT4 was a mixture of the following components: MPP635VF micropowder 100 dry parts TRITON X100 3 dry parts MICHEM Prime 4983 100 dry parts The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The surface meltable coating was applied to provide a dry coating weight of 3.0 lb./144 yd or about 11.3 gsm.

PCT5 Surface meltable coating PCT5 was identical to PCT4 except that the surface meltable coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.1 gsm.

PCT6 Surface meltable coating PCT6 was a mixture of the following components: MPP635G micropowder 100 dry parts TRITON X100 3 dry parts MICHEM Prime 4983 200 dry parts MPP635G micropowder is a micronized high density polyethylene powder having an average particle size of 12 microns, available from Micropowders, Inc., Scarsdale, NY.

The mixture was dispersed in a Colloid mill. The total solids content was 25 wt% total dry solids in water. The surface meltable coating was applied to provide a dry coating weight of 3.0 lb./144 yd2 or about 11.3 gsm.

PCT7 Surface meltable coating PCT7 was identical to PCT6 except that the surface meltable coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.1 gsm.

PCT8 Surface meltable coating PCT8 was a mixture of the following components: MICHEM Prime 4990 100 dry parts ORGASOL 3501 EXDNAT 1 40 dry parts BENZOFLEX 352 20 dry parts MPP635VF micropowder 20 dry parts TRITON X100 3 dry parts MICHEM Prime 4990 is an ethylene-acrylic acid copolymer dispersion available from Michelman, Chemical Company, Cincinnati, OH.

ORGASOL 3501 EXDNAT 1 is a 10 micron average particle size co-polyamide 6-12 available from Elf Atochem, Paris, France.

BENZOFLEX 352 is a cyclohexane dimethanol dibenzoate <BR> <BR> R<BR> <BR> powder available from VELSICOL Chemical Corporation, Rosemont, IL.

The BENZOFLEX 352 powder was ground to an average particle size of about 8 microns by Powdersize, Inc., Quakertown, PA.

The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The surface meltable coating was applied to provide a dry coating weight of 3.0 lb./144 yd2 or about 11.3 gsm.

PCT9 Surface meltable coating PCT9 was identical to PCT8 except that the surface meltable coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.1 gsm.

Print Coating (Surface Meltable) Layers-Laser Copiers The following surface meltable coatings were used with Laser copiers. Each coating was applied using a Meyer rod technique and dried in a forced air oven at about 200°F (93°C).

LCP1 Surface meltable coating LCP1 was identical to PCT8.

LCP2 Surface meltable coating LCP2 was identical to PCT9.

LCP3 Surface meltable coating LCP3 was identical to PCT8 except that the surface meltable coating was applied to provide a dry coating weight of 2.0 lb./144 yd2 or about 7.5 gsm.

LCP4 Surface meltable coating LCP4 was identical to PCT4.

LCP5 Surface meltable coating LCP5 was a mixture of the following components: MICHEM Prime 4990 100 dry parts ORGASOL 3501 EXDNAT 1 100 dry parts TRITON X100 5 dry parts The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The surface meltable coating was applied to provide a dry coating weight of 2.5 lb./144 yd2 or about 9.4 gsm.

LCP6 Surface meltable coating LCP6 was a mixture of the following components: MICHEM Prime 4990 100 dry parts ALMACRYL P-501 100 dry parts TRITON X100 3 dry parts

ALMACRYL P-501 is a powdered polyester available from Image Polymers Inc., Wilmington, MA The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The surface meltable coating was applied to provide a dry coating weight of 2.3 lb./144 yd2 or about 8.7 gsm.

Print Coating (Surface Meltable) Layers-Ink jet Printers The following surface meltable coatings were used with ink jet printers. Each coating was applied using a Meyer rod technique and dried in a forced air oven at about 180°F (82°C).

PHI Ink jet print coating PIJ1 was a mixture of the following components: ORGASOL 3501 EXDNAT 1 100 dry parts ALMACRYL) P-501 50 dry parts MICHEM Prime 4990 25 dry parts TERGITOL 15-S40 5 dry parts Sodium carbonate 2 dry parts POLYOX N60K 4 dry parts ALCOSTAT 567 2 dry parts METHOCEL A-15 1 dry part ALCOSTAT 567 is a poly (N, N-dimethylethylamino methacrylate), quaternized with methyl chloride, available from Allied Colloids (Suffolk, VA) as a water solution.

METHOCEL A-15 is a methylcellulose available from Dow Chemical Company, Midland, MI.

The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 5.5 lb./144 yd2 or about 20.7 gsm.

PIU2 Ink jet print coating PIJ2 was a mixture of the following components: ORGASOL 3501 EXDNAT 1 100 dry parts MICHEM Prime 4990 25 dry parts TRITON X100 5 dry parts Sodium carbonate 1 dry part POLYOX N60K 2 dry parts The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.1 gsm.

Piu3 Ink jet print coating PIJ3 was a mixture of the following components: ORGASOL 3501 EXDNAT 1 100 dry parts MICHEM Prime 4990 45 dry parts TRITON X100 5 dry parts Sodium carbonate 1 dry part KLUCELt) L 5 dry parts BENZOFLEX 352 40 dry parts The BENZOFLEX 352 powder was ground to an average particle size of about 8 microns by Powdersize, Inc. The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 3.5 lb./144 yd2 or about 13.2 gsm.

Pipi4 Ink jet print coating PIJ4 was identical to PIJ3 except that the ink jet print coating was applied to provide a dry coating weight of 5.0 lb./144 yd2 or about 18.9 gsm.

PIJ5 Ink jet print coating PIJ5 was a mixture of the following components: ORGASOL# 3501 EXDNAT 1 100 dry parts AIRFLEX 540 10 dry parts POLYOX N60K 10 dry parts ALCOSTAT 167 5 dry parts TRITON X100 5 dry parts AIRFLEX 540 is an ethylene-vinyl acetate copolymer binder available from Air Products, Allentown, PA.

The mixture was dispersed in a Colloid mill. The total solids content was 17 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 2.5 lb./144 yd2 or about 9.4 gsm.

Pu Ink jet print coating PIJ6 was a mixture of the following components: ORGASOL 3501 EXDNAT 1 100 dry parts AIRFLEX 540 20 dry parts POLYOX N60K 5 dry parts ALCOSTAT 167 2.5 dry parts TRITON X100 5 dry parts The mixture was dispersed in a Colloid mill. The total solids content was 23 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 4.0 lb./144 yd or about 15.1 gsm.

PIJ7 Ink jet print coating PIJ7 was a mixture of the following components: ORGASOL 3501 EXDNAT 1 100 dry parts

MICHEM Prime 4990 25 dry parts TRITON X100 5 dry parts Sodium carbonate 1 dry part POLYOX#POLYOX#N60K 2 parts ALCOSTAT 167 3 dry parts The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 5.0 lb./144 yd2 or about 18.9 gsm.

PIJ8 Ink jet print coating PIJ8 was a mixture of the following components: ORGASOL# 3501 EXDNAT 1 100 dry parts MICHEM Prime 4990 45 dry parts TRITON X100 5 dry parts Sodium carbonate 1 dry part KLUCEL (E) L dry parts BENZOFLEX# 352 40 dry parts ALCOSTAT 167 3 dry parts The BENZOFLEX 352 powder was ground to an average particle size of about 8 microns by Powdersize, Inc. The mixture was dispersed in a Colloid mill. The total solids content was 30 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 5.0 lb./144 yd2 or about 18.9 gsm.

PIJ9 Ink jet print coating PIJ9 was a mixture of the following components: ORGASOL 3501 EXDNAT 1 100 dry parts MICHES) Prime 4990 25 dry parts TRITON X100 5 dry parts

POLYOX N60K 2 dry parts ALCOSTAT 167 5 dry parts The mixture was dispersed in a Colloid mill. The total solids content was about 25 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.0 gsm.

PIJ10 Ink jet print coating PIJ10 was a mixture of the following components: ORGASOL# 3501 EXDNAT 1 100 dry parts MICHEM Prime 4990 25 dry parts AIRFLEX 540 10 dry parts TRITON X100 5 dry parts POLYOX N60K 1 dry parts ALCOSTAT 167 2 dry parts The mixture was dispersed in a Colloid mill. The total solids content was about 25 wt% total dry solids in water. The print coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.0 gsm.

PIJ11 Ink jet print coating PIJ11 was a mixture of the following components: TRITON X100 1 dry part BENZOFLEX 352 41.2 dry parts KLUCEL L 5 dry parts ORGASOL 3501 EXDNAT 1 100 dry parts MICHEM Prime 4990R 85 dry parts KLUCEL L/ALCOSTAT# 167 8 dry parts ammonia 2 parts

KLUCEL L is a hydroxypropyl cellulose available from Hercules, Wilmington, DE.

ALCOSTAT 167 is a poly (diallyldimethylammonium) chloride, available from Allied Colloids (Suffolk, VA) as a water solution.

The BENZOFLEX 352 powder was ground to an average particle size of about 8 microns by Powdersize, Inc., Quakertown, PA.

The first four components of the mixture were dispersed in a Cowles dissolver for about 30 minutes. The MICHEM Prime 4990R and ammonia were then added. Lastly, the KLUCEL L/ALCOSTAT 167 mixture was added. The KLUCEL L/ALCOSTAT 167 mixture comprised 1 dry part KLUCEL L and 3 dry parts ALCOSTAT 167.

The total solids content of the coating was 23.8 wt% total dry solids in water. The surface meltable coating was applied to provide a dry coating weight of 4.5 lb./144 yd2 or about 17.0 gsm.

Sub-Coating Layers The following layers were used as sub-coating layers between a release layer and a print coating layer, particularly ink jet print coating layers. Each coating was applied using a Meyer rod technique and dried in a forced air oven at about 200°F (93°C).

SC1 Sub-coating SC1 was a mixture of the following components: MICHEM Prime 4990 100 dry parts TRITON X100 3 dry parts The total solids content was about 30 wt% total dry solids in water. The sub-coating was applied to provide a dry coating weight of 1.9 lb./144 yd2or about 7.2 gsm.

SC2 Sub-coating SC2 was identical to LCP5.

SC3 Sub-coating SC3 was identical to LCP6.

SC4 Sub-coating SC4 was a mixture of the following components: HYCAR# 26672 100 dry parts TERGITOL 15-S40 3 dry parts The total solids content was about 20 wt% total dry solids in water. The sub-coating was applied to provide a dry coating weight of 0.7 lb./144 yd2or about 2.6 gsm.

SC5 Sub-coating SC5 was a mixture of the following components: HYCAR# 26672 50 dry parts MICHEM Prime 4990 50 dry parts TERGITOL 15-S40 3 dry parts The total solids content was about 30 wt% total dry solids in water. The sub-coating was applied to provide a dry coating weight of 1.8 lb./144 yd2 or about 6.8 gsm.

SC6 Sub-coating SC6 was a mixture of the following components: MICHEM Prime 4983 100 dry parts The total solids content was about 25 wt% total dry solids in water. The sub-coating was applied to provide a dry coating weight of 2.0 lb./144 yd2 or about 7.5 gsm.

SC7 Sub-coating SC7 was identical to PCT8.

SC8 Sub-coating SC8 was a mixture of the following components: BENZOFLEX# 352 50 dry parts ORGASOL 3501 EXDNAT 1 25 dry parts

MICHEM Prime 4990 35 dry parts The BENZOFLEX 352 powder was ground to an average particle size of about 8 microns by Powdersize, Inc. The mixture was dispersed in a Colloid mill. The total solids content was about 30 wt% total dry solids in water. The sub-coating was applied to provide a dry coating weight of 3.0 lb./144 yd2 or about 11.3 gsm.

SC9 Sub-coating SC9 was a mixture of the following components: BENZOFLEX 352 70 dry parts MICHEM Prime 4990 30 dry parts TRITON X100 2.1 dry parts The BENZOFLEX 352 powder was ground to an average particle size of about 8 microns by Powdersize, Inc. The mixture was dispersed in a Colloid mill. The total solids content was about 30 wt% total dry solids in water. The sub-coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.1 gsm.

SC10 Sub-coating SC10 was a mixture of the following components: MICHEM Prime 4990 100 dry parts ORGASOL 3501 EXDNAT 1 40 dry parts TRITON X100 2 dry parts The mixture was dispersed in a Colloid mill. The total solids content was about 30 wt% total dry solids in water. The sub-coating was applied to provide a dry coating weight of 4.0 lb./144 yd2 or about 15.1 gsm.

SC11 Sub-coating SC11 was a mixture of the following components: MICHEM Prime 4990 100 dry parts ORGASOL 3501 EXDNAT 1 40 dry parts

BENZOFLEX 352 40 dry parts TERGITOL 15-S40 2 dry parts POLYOX N60K 1 dry parts ammonia 0.55 parts isopropyl alcohol drops (to defoam) TERGITOL 15-S40 is an ethoxylated alcohol surfactant available from Union Carbide (Danbury, CT).

The BENZOFLEX 352 powder was ground to an average particle size of about 8 microns by Powdersize, Inc., Quakertown, PA.

The mixture was dispersed in a Cowles dissolver, a high shear mixer, for about 30 minutes. The total solids content was 33.8 wt% total dry solids in water. Drops of isopropyl alcohol were added as needed to control foaming. The surface meltable coating was applied to provide a dry coating weight of 4.5 lb./144 yd2 or about 17.0 gsm.

Top Coat Layers The following layer was used as a top coating layer for overcoating a print coating layer, particularly ink jet print coating layers. The layer was applied using a Meyer rod technique and dried in a forced air oven at about 180°F (82°C).

TC1 Top coating layer TC1 was a mixture of the following components: POLYOX (E) N60K 66 dry parts ALCOSTAT 167 0.66 dry parts KLUCEL L 0.33 dry parts The mixture was dispersed in a Colloid mill. The total solids content was 1.65 wt% total dry solids in water. The top coating was applied to provide a dry coating weight of 0.25 lb./144 yd or about 0.9 gsm.

EXAMPLE 1 Preparation of Heat Transfer Materials Having a Thermal Ribbon Printed ImageThereon Heat transfer materials were prepared from the above- described layers. The components of the heat transfer materials are shown below in Table 1. Images were printed onto the heat transfer materials using a thermal ribbon printer.

Table 1. Thermal Ribbon Printable Designs Sample # Base Paper Base Coat Release Print Coat Coat TR1 BP3 BC1 RC1 PCT1 TR2 BP3 BC1 RC2 PCT2 TR3 BP3 BC1 RC2 PCT4 TR4 BP3 BC1 RC3 PCT4 TR5 BP3 BC1 RC4 PCT4 TR6 BP3 BC1 RC5 PCT4 TR7 BP3 BC1 RC5 LCP5 TR8 BP1 BC2 RC6 LCP5 TR9 BP1 BC2 RC6 LCP6 TR10 BP1 BC2 RC6 PCT4 TR11 BP1 BC2 RC 13 PCT2 TR12 BP1 BC2 RC14 PCT4 TR13 BP1 BC2 RC14 PCT9 TR14 BP1 BC2 RC15 PCT6 TR15 BP1 BC2 RC16 PCT9 TR16* BP3 BC1 NONE PCT1 * Comparative example having no release coat.

For good thermal ribbon printing results, smoothness of the base substrate is known to be a desirable factor. Better printing results are obtained when there is good contact between the heat transfer sheet and the ribbon. Further, the smoothness of the surface meltable (print) coating layer is known to be a desirable factor for producing good print results. Better print results are obtained when the surface meltable (print) coating bonds well to the wax ribbon pigments.

Coatings containing meltable ethylene-acrylic acid copolymer binders with meltable, fine particulate polymers worked particularly well.

A surface meltable layer coating basis weight of as little as about 3 lb. per 144 yd2 (11.3 gsm) was suitable for use with the thermal ribbon printers.

Each sample was tested for color wash retention,"hand,"and tackiness. As used herein, the term"hand"is used in its customary way (i. e., the feel and stiffness of a given sample). The results are given in Table 4 below.

EXAMPLE 2 Preparation of Heat Transfer Materials Having a Laser Color Copier Printed Image Thereon Heat transfer materials were prepared from the above- described layers using the procedure outlined in Example 1. The components of the heat transfer materials are shown below in Table 2.

Images were copied onto the heat transfer materials using a Canon 700 laser color copier.

Table 2. Color Laser Copier Designs Sample Base Paper Base Coat Release Print Coat Coat CLC1 BP1 BC2 RC5 PCT4 CLC2 BP1 BC2 RC5 LCP5 CLC3 BP1 BC2 RC5 LCP6 CLC4 BP1 BC2 RC14 PCT8 CLC5 BP1 BC2 RC14 PCT9 CLC6 BP1 BC2 RC14 LCP3 CLC7 BP1 BC2 RC16 PCT9 CLC8* BP1 BC2 CLC9** BP6 RC10 BC1 * Comparative example using hot removal of paper, having a single layer of meltable coating.

** Comparative example using cold removal of paper, having a release coat and an outside single layer of meltable coating.

Bond papers such as BP1 and BP6 in the tables above worked well for photocopier grades, due to their stiffness, conductivity, caliper, and smoothness required for photocopying.

For photocopying, the surface meltable or top coating does not need to be as smooth as in thermal ribbon printing. Very similar coating compositions to the thermal ribbon types worked well for photocopying.

A surface meltable layer coating basis weight of as little as about 3 lb. per 144 yd2 (11.3 gsm) was suitable for use with photocopying.

Each sample was tested for color wash retention,"hand,"and tackiness. The results are given in Table 5 below.

EXAMPLE 3 Preparationof Heat Transfer Materials Having an Ink Jet Printed Image Thereon Heat transfer materials were prepared from the above- described layers using the procedure outlined in Example 1. The components of the heat transfer materials are shown below in Table 3.

Images were printed onto the heat transfer materials using an ink jet printer.

Table 3. Ink Jet Printable Designs Sample Base Base Coat Release Sub-Print Top Coat Paper Coat Coat Coat IJ1 BP3 BC1 RC6 SC1 PIJ1 NONE IJ2 BP3 BC1 RC6 LCP5 PIJ1 NONE (SC2) IJ3 BP3 BC1 RC6 LCP6 PIJ1 NONE (SC3) BC3RC6SC4PIJ1NONEIJ4BP2 BC3RC6SC5PIJ1NONEIJ5BP2 BC1RC10NONEPIJ2TC1IJ6BP2 IJ7 BP 1 BC2 RC11 NONE PIJ2 TC1 IJ8 BP1 BC2 RC11 SC6 PIJ2 TC1 BC2RC11SC7PIJ2TC1IJ9BP1 (PCT8) BC2RC11SC8PIJ2TC1IJ10BP1 IJ11 BP1 BC2 RC11 SC9 PIJ2 TC1 IJ12 BP1 BC2 RC11 NONE PIJ2 NONE IJ13 BP1 BC2 RC11 NONE PIJ3 TC1 IJ14 BP 1 BC2 RC12 NONE PIJ2 NONE IJ15 BP1 BC2 RC12 NONE PIJ2 TC1 BC2RC12PCT8PIJ2NONEIJ16BP1 IJ17 BP1 BC2 RC12 PCT8 PIJ2 TC1 IJ18 BP1 BC2 RC12 NONE PIJ5 NONE BC2RC12NONEPIJ6NONEIJ19BP1 BC2RC10NONEPIJ6NONEIJ20BP1 IJ21 BP 1 BC2 RC10 NONE PIJ9 NONE BC2RC10NONEPIJ4TC1IJ22BP1 BC2RC13NONEPIJ4TC1IJ23BP1 IJ24 BP1 BC2 RC14 NONE PIJ4 TC1 IJ25 BP1 BC2 RC13 SC9 PIJ4 TC1 BC2RC14SC9PIJ4TC1IJ26BP1 IJ27 BP1 BC2 RC 13 NONE PIJ7 NONE 1BC2RC13SC9PIJ7NONEIJ28BP BC2RC13NONEPIJ8NONEIJ29BP1 IJ30 BP1 BC2 RC17 NONE PIJ8 NONE NONERC10BC1PIJ2TC1IJ31*BP6 IJ32* BP 6 NONE RC10 BC1 PIJ3 TC1 IJ33BP3NONENONEBC1PIJ2TC1 IJ34 BP7 BC4 RC12 SC10 PIJ10 NONE IJ35 BP7 BC4 RC12 SC9 PIJ10 NONE IJ36 BP7 BC4 RC18 SC10 PIJ10 NONE IJ37 BP7 BC5 RC12 SC10 PIJ10 NONE IJ38 BP7 BC5 RC18 SC10 PIJ10 NONE IJ39 BP6 BC5 RC19 SC11 Pljll NONE

* Comparative example having a meltable layer only on the outer surface of the release coat. Cold removal of paper.

** Comparative example having no release coat and hot removal of paper.

For ink jet printing, any of the base papers were suitable. As far as ink jet printing results, surface meltable or top coating containing polyamide powder, ORGASOL# 3501 EXD NAT 1, provided the best results. The polyamide powders were very receptive to the ink jet inks. Further, the melting point and melt viscosity were low enough and the particle size was particularly suitable for the formation of a microporous coating.

MICHEM Prime EAA suspensions were again determined to be the binders of choice, although acceptable results were also obtained with an EVA latex, AIRFLEX# 540. AIRFLEX# 540 AIRFLEX not melt and flow as well as the MICHEM Prime EAA suspensions.

Retention of the ink jet inks was enhanced by the addition of a cationic polymer, particularly ALCOSTAT 167. ALCOSTAT 167 was determined to be compatible with the non-ionic latex AIRFLEX 540.

Compatibility of ALCOSTAT 167 with anionic MICHEM Prime 4990 was improved by the addition of TRITON X100 and KLUCEL L or POLYOXt) N60K.

For ink jet printing, better print results were obtained with a surface meltable coating basis weight of from about 4.0 lb./144 yd2 to about 5.0 lb./144 yd2.

Each sample was tested for color wash retention,"hand,"and tackiness. The results are given in Table 6 below.

EXAMPLE 4 Testing of Heat Transfer Materials Having a Thermal Ribbon Printed Image Thereon Transfers of the images were made using a hand ironing technique or a heating press. A cushioning material was placed onto a hard surface. A piece of cloth or blotter paper was suitable as a cushioning material. A substrate to be coated was then placed onto the cushioning material. Then, the heat transfer material was placed onto the substrate.

When an iron was used, the heat transfer material was ironed for three minutes, applying pressure onto the heat transfer material.

The ironing strokes were slow and in the longest direction of the heat transfer material. The iron used was a Procter-Silex model 17109 or 13117. When a heating press was used, the heat transfer material was pressed for up to 30 seconds. The images were multi-colored test patterns covering nearly all the heat transfer material surface. The heat transfer material was removed after cooling.

The heat transfer materials described in Table 1 above were transferred to substrates using a hot or cold peelable method. The substrates used were either 100% cotton T-shirt material (cotton) or 50/50 cotton/polyester (cotton/poly) material. The heat pressed samples were pressed for 30 sec at 350°F using a Hix Model 600 press from Hix Corporation, Pittsburg, KS. A few of the heat pressed samples were also pressed for 10 sec at 350°F using the same equipment.

The coated substrates were tested for the following properties: color wash retention,"hand,"and tackiness. For each property, a number value from"1"to"5"was assigned. The rating system is explained below.

A rating of"5"in color retention indicated that there was a noticable, but small, decrease in color intensity after five washings. A rating of"1"indicated that very little color remained after five washings. Ratings of"2"to"4"indicated progressively poorer color retention from"4"to"2".

A rating of"5"in hand indicated that the difference in feel between the original fabric and the image-bearing fabric was barely noticable. A rating of"1"indicated that the image-bearing fabric was very stiff, smooth, and non-porous. Ratings of"2"to"4"indicated progressively poorer hand from"4"to"2".

A rating of"5"in tackiness indicated that two image-bearing fabrics did not adhere to one another after being pressed together on a heat transfer press at 215°F and subsequently cooled. A rating of"1" indicated that the two image-bearing fabrics adhered strongly to one another after the above-described test, resulting in damaged images.

Ratings of"2"to"4"indicated progressively more tackiness from"2" to"4".

The testing results are shown below in Table 4.

Table 4. Thermal Ribbon Print Test Results Sample Fabric Transfer Paper Color"Hand"Tacki-Other Method Removal Wash ness Retention TR1 Cotton Press Hot 1 5 5 1 TR2 Cotton Press Hot 2 5 5 TR3 Cotton Press Hot 3 5 5 TR4 Cotton Press Hot 1 5 5 1 TR5 Cotton Press Cold 3 3 5 2,3 TR6 Cotton Press 3 5 Cold TR7 Cotton Press Cold 3 5 5 2 TR8 Cotton Press Cold 3 5 5 2 TR9 Cotton Press Cold 3 5 5 2 TR10 Cotton Press Cold 3 5 5 2 TR11 Cotton/Press Cold 3 4 5 4 Poly TR12 Cotton/Press Cold 4 4 5 4 Poly TR13 Cotton/Press Cold 5 4 5 4 Poly TR14 Cotton/Press Hot 4 5 5 6 Poly TR13 Cotton Iron Cold 5 4 5 6 TR14 Cotton/Iron Hot 5 5 5 Poly TR15 Cotton/Press* Hot 4 5 5 Poly TR15 Cotton/Iron Hot 5 5 5 Poly TR16 Cotton/Press* Hot 4 3 3 7 Poly

* Transferred well after 10 sec. pressing also.

Other key: 1. Incomplete transfer.

2. The surface meltable (print) coating contained voids due to the water repellancy of the release coating.

3. Some of the interior meltable coating actually went through the release coating and into the fabric; the release coating still functioned.

4. The surface meltable (print) coating became loose while processing through the printer, as the coating had a tendency to adhere to the wax ribbon.

5. The paper was difficult to remove after ironing; this was not the case with the efficient, rapid, heating of the heating press.

6. Print was somewhat grainy.

7. Comparative example.

EXAMPLE 5 Testing of Heat Transfer Materials Having a Laser Color Copier Printed Image Thereon The heat transfer materials described in Table 2 above were transferred to substrates and tested using the heat transfer procedure and testing procedure as outlined in Example 4. The testing results are shown below in Table 5.

Table 5. Laser Copier Test Results Sample Fabric Transfer Paper Color"Hand"Tacki-Other Method Removal Wash ness Retention Cotton Press Cold 2 5 5 1 CLC2 Cotton Press Cold 3 5 5 1 CLC3 Cotton Press Cold 4 5 5 1 CLC4 Cotton/Press Cold 4 4 5 Poly CLC5 Cotton/Press Cold 5 4 5 Poly CLC5 Cotton/Iron Cold 5 4 5 Poly CLC5 Cotton/Press Hot 5 5 5 Poly CLC6 Cotton/Press Cold 4 4 5- Poly CLC7 Cotton/Press Hot 5 5 5- Poly CLC8 Cotton/Press Hot 4 3 2 2 Poly

CLC9 Cotton/Press Hot 3 3 4 2 Poly Other key: 1. The surface meltable (print) coating had some voids due to the water repellancy of the release coating.

2. Comparative sample.

EXAMPLE 6 Testingof Heat Transfer Materials Having an Ink Jet Printed Image Thereon The heat transfer materials described in Table 3 above were transferred to substrates and tested using the heat transfer procedure and testing procedure as outlined in Example 4. The testing results are shown below in Table 6.

Table 6. Ink Jet Printable Test Results Sample Fabric Transfer Paper Color"Hand"Tacki-Other Method Removal Wash ness Retention IJ 1 Cotton Press Cold 4 5 5 1,2 IJ2 Cotton Press Cold 5 1,2,3 IJ3 Cotton Press Cold 4 5 5 1,2 IJ4 Cotton Press Cold 4 5 5 1,2 IJ5 Cotton Press Cold 4 5 5 1,2 IJ6 Cotton/Iron Cold 4 3 3 1,4 Poly IJ7 Cotton/Iron Cold 4 4 5 1,4 Poly IJ7 Cotton/Press Cold 5 4 5 1 Poly IJ7 Cotton/Press Cold 5 4 5 5 Poly IJ7 Cotton/Press Cold 4 4 5 6 Poly IJ8 Cotton/Iron Cold 5 4 5 1,3 Poly IJ9 Cotton/Iron Cold 5 4 5 1,3 Poly IJ10 Cotton/Iron Cold 5 4 5 1 Poly IJ11 Cotton/Iron Cold 5 4 5 1 Poly Ull Cotton/Press Cold 5 5 5 5 Poly IJ11 Cotton/Iron Cold 5 4 5 6 Poly IJ12 Cotton/Press Cold 4 4 5 1 Pot IJ12 Cotton/Press Cold 4 4 5 5 Poly IJ12 Cotton/Press Cold 3 4 5 6 Poly IJ13 Cotton/Press Cold 3 4 5 6 Poly IJ14 Cotton/Iron Cold 4 4 5 1 Poly IJ15 Cotton/Press Cold 4 4 5 1 Poly IJ16 Cotton/Iron Cold 4 4 5 1 Poly IJ16 Cotton/Iron Cold 4 4 5 5 Poly IJ16 Cotton/Iron Cold 3 4 5 6 Poly IJ17 Cotton/Press Hot 5 5 5 1 Poly IJ17 Cotton/Iron Cold 5 4 5 1 Poly IJ17 Cotton/Iron Cold 5 4 5 5 Poly IJ17 Cotton/Iron Cold 5 4 5 6 Poly IJ18 Cotton/Iron Cold 2 5 5 1,4 Poly IJ18 Cotton/Press Cold 2 5 5 1,4 Poly IJ19 Cotton/Press Cold 4 4 5 1 Poly IJ19 Cotton/Iron Cold 4 4 5 1,4 Poly IJ20 Cotton/Iron Cold 4 3 4 1,4 Poly IJ21 Cotton/Iron Cold 3 4 4 1,4 Poly IJ22 Cotton/Press Cold 4 4 5 1 Poly IJ23 Cotton/Press Cold 4 4 5 1 Poly IJ24 Cotton/Press Cold 4 4 5 1 Poly IJ25 Cotton/Iron Cold 5 4 5 1 Poly IJ25 Cotton/Iron Cold 5 4 5 5 Poly IJ25 Cotton/Iron Cold 5 4 5 5 Pot IJ25 Cotton/Press Hot 5 5 5 1 1 Poly IJ26 Cotton/Press Cold 5 4 5 1 Poly IJ27 Cotton/Press Cold 5 4 5 1 Poly IJ27 Cotton/Press Cold 5 4 5 5 Pol IJ27 Cotton/Press Cold 5 4 5 6 Poly IJ28 Cotton/Press Cold 5 4 5 1 Poly IJ28 Cotton/Press Cold 5 4 5 5 Poly IJ28 Cotton/Press Cold 5 4 5 6 Pol IJ29 Cotton/Press Cold 5 4 5 1 Poly IJ29 Cotton/Press Cold 5 4 5 5 Pol IJ29 Cotton/Press Cold 4 4 5 6 Poly IJ29 Cotton/Iron Cold 5 4 5 1 Poly IJ30 Cotton/Press Cold 5 4 5 1 Poly IJ31 Cotton/Iron Cold 4 2 2 6,7 Pol IJ31 Cotton/Press Cold 4 3 3 6,7 Poly IJ32 Cotton/Press Cold 4 3 3 6,4 Poly IJ32 Cotton/Iron Cold 4 3 3 6,7 Poly IJ33 Cotton/Press Hot 4 4 3 1 Pol IJ33 Cotton/Iron Hot 4 4 3 1,8 Poly IJ33 Cotton/Press Hot 4 4 3 5 Pol IJ33 Cotton/Press Hot 4 4 3 5 Poly IJ34 Cotton Press Cold 4 4 5 9 IJ34 Cotton Iron Cold 4 4 5 9 IJ35 Cotton Press Cold 3 4 5 9 IJ35 Cotton Iron Cold 4 4 5 9 IJ35 Cotton Press Cold 4 4 5 9 IJ36 Cotton Press Cold 4 4 5 9 IJ37 Cotton Press Cold 4 4 5 9 IJ38 Cotton Press Cold 4 4 5 8,9 IJ39 Cotton Press Cold 4 4 5 6 IJ39 Cotton Iron Cold 4 4 5 6

Other key: 1. Canon BJ600 Printer 2. There were voids in the sub-coating and/or surface meltable (print) coating due to water repellency of the release coating.

3. Some of the interior meltable coating actually went through the release coating and into the fabric; the release coating still functioned.

4. Slight cracking of the image-bearing coating after 5 washes.

5. Epson Stylus 800 printer 6. Hewlett Packard 694 Printer 7. Moderate to severe cracking of the image- bearing coating after 5 washes.

8. The paper was hard to remove. The image- bearing coating of the fabric stretched and became distorted.

9. Epson Photo Stylus Printer.

While the specification has been described in detail with respect to specific embodiments thereof, it will be appreciated that those skilled in the art, upon attaining an understanding of the foregoing, may readily conceive of alterations to, variations of, and equivalents to these embodiments. Accordingly, the scope of the present invention should be assessed as that of the appended claims and any equivalents thereto.