Image transfer sheet

Information

  • Patent Grant
  • 8541071
  • Patent Number
    8,541,071
  • Date Filed
    Monday, April 16, 2012
    12 years ago
  • Date Issued
    Tuesday, September 24, 2013
    11 years ago
Abstract
The present invention includes an article and method for transferring an image from one substrate to another. The method includes providing or obtaining an image transfer sheet that is comprised of a substrate layer, a release layer and an image-imparting layer that may comprise a low density polyethylene or other polymeric component having a melting temperature within a range of about 90 degrees C. to about 700 degrees C. An image is imparted to the low density polyethylene area with an image-imparting medium. A second image receiving substrate can be provided. The second image receiving substrate is contacted to the first image transfer sheet at the polymer, image-imparting layer. Heat is applied to the image transfer sheet so that the low density polyethylene encapsulates the image-imparting medium and transfers the encapsulates to the image receiving substrate, thereby forming a mirror image on the image receiving substrate.
Description
BACKGROUND

Image transfer to articles made from materials such as fabric, nylon, plastics and the like has increased in popularity over the past decade due to innovations in image development. On Feb. 5, 1974, La Perre et al. were issued a United States Patent describing a transfer sheet material markable with uniform indicia and applicable to book covers. This sheet material included adhered plies of an ink-receptive printable layer and a solvent-free, heat-activatable adhesive layer. The adhesive layer was somewhat tacky prior to heat activation to facilitate positioning of a composite sheet material on a substrate which was to be bonded. The printable layer had a thickness of 10 to 500 microns and had an exposed porous surface of thermoplastic polymeric material at least 10 microns thick.


Indicia were applied to the printable layer with a conventional typewriter. A thin film of temperature-resistant, low surface energy polymer, such as polytetrafluoroethylene, was laid over the printed surface and heated with an iron. Heating caused the polymer in the printable layer to fuse thereby sealing the indicia into the printable layer.


On Sep. 23, 1980, Hare was issued U.S. Pat. No. 4,224,358, which described a kit for applying a colored emblem to a t-shirt. The kit comprised a transfer sheet which included the outline of a mirror image of a message. To utilize the kit, a user applied a colored crayon to the transfer sheet and positioned the transfer sheet on a t-shirt. A heated instrument was applied to the reverse side of the transfer sheet in order to transfer the colored message.


The Greenman et al. patent, U.S. Pat. No. 4,235,657, issuing Nov. 25, 1980, described a transfer web for a hot melt transfer of graphic patterns onto natural, synthetic fabrics. The transfer web included a flexible substrate coated with a first polymer film layer and a second polymer film layer. The first polymer film layer was made with a vinyl resin and a polyethylene wax which were blended together in a solvent or liquid solution. The first film layer served as a releasable or separable layer during heat transfer. The second polymeric film layer was an ionomer in an aqueous dispersion. An ink composition was applied to a top surface of the second film layer. Application of heat released the first film layer from the substrate while activating the adhesive property of the second film layer thereby transferring the printed pattern and a major part of the first layer along with the second film layer onto the work piece. The second film layer bonded the printed pattern to the work piece while serving as a protective layer for the pattern.


The Sanders et al. patent, U.S. Pat. No. 4,399,209, issuing Aug. 16, 1983, describes an imaging system in which images were formed by exposing a photosensitive encapsulate to actinic radiation and rupturing the capsules in the presence of a developer so that there was a pattern reaction of a chromogenic material present in the encapsulate or co-deposited on a support with the encapsulate and the developer which yielded an image.


The Goffi patent, U.S. Pat. No. 4,880,678, issuing Nov. 14, 1989, describes a dry transfer sheet that comprises a colored film adhering to a backing sheet with an interposition of a layer of release varnish. The colored film included 30% to 40% pigment, 1% to 4% of cycloaliphatic epoxy resin, from 15% to 35% of vinyl copolymer and from 1% to 4% of polyethylene wax. This particular printing process was described as being suitable for transferring an image to a panel of wood.


The Kronzer et al. patent, U.S. Pat. No. 5,271,990, issuing Dec. 21, 1993, describes an image-receptive heat transfer paper that included a flexible paper based web base sheet and an image-receptive melt transfer film that overlaid a top surface of the base sheet. The image-receptive melt transfer film was comprised of a thermoplastic polymer melting at a temperature within a range of 65 degrees C. to 180 degrees C.


The Higashiyami et al. patent, U.S. Pat. No. 5,019,475, issuing May 28, 1991, describes a recording medium that included a base sheet, a thermoplastic resin layer formed on at least one side of the base sheet and a color developer layer formed on a thermoplastic resin layer and capable of color development by reaction with a dye precursor.





BRIEF DESCRIPTION OF THE DRAWINGS

The drawing illustrates generally, by way of example, but not by way of limitation, one embodiment discussed in the present document.



FIG. 1 illustrates a cross-sectional view of one embodiment of an image transfer sheet of the present invention.





SUMMARY

One embodiment of the present invention includes a method for transferring an image from one substrate to another. The method comprises providing an image transfer article, such as a sheet, which is comprised of a substrate layer, a release layer and an image-imparting layer that comprises a polymer component such as a low density polyethylene (LDPE) or Ethylene Acrylic Acid (EAA) or Ethylene Vinyl Acetate (EVA) or Methane Acrylic Ethylene Acrylic (MAEA) or mixtures of these materials, each having a melt index within a range of about 20 to about 1,200 degrees C.-g/10 minute (SI). An image is imparted to the polymer component of the image imparting layer through an image imparting medium such as ink or toner.


In one embodiment, an image receiving substrate is also provided. The image receiving substrate is contacted to the image transfer sheet and is specifically contacted to the polymer component of the image imparting layer. Heat is applied to the substrate layer of the image transfer sheet and is transferred to the polymer component of the image imparting layer so that the polymer, such as the LDPE, EAA, EVA, or MAEA encapsulates the image-imparting medium and transfers the encapsulates to the image receiving substrate thereby forming a mirror image on the image receiving substrate.


One other embodiment of the present invention includes an image transfer sheet that comprises a substrate layer, a release layer and an image imparting layer that comprises a polymeric layer such as a low density polyethylene layer, an EAA layer, an EVA layer, or an MAEA layer. An image receptive layer is a top polymer layer.


With one additional embodiment, an image transfer sheet of the present invention comprises an image imparting layer but is free from an image receptive layer such as an ink receptive layer. Image indicia are imparted, with this embodiment, using techniques such as color copy, laser techniques, toner or by thermo transfer from ribbon wax or from resin.


The LDPE polymer of the image imparting layer melts at a point within a range of about 43 degrees C. to about 300 degrees C. The LDPE has a melt index (MI) of about 60 to about 1,200 SI-g/10 minute.


The EAA has an acrylic acid concentration ranging from about 5% to about 25% by weight and has a MI of about 20 to about 1300 g/10 minutes. A preferred EAA embodiment has an acrylic acid concentration of 7% to 20% by weight and an MI range of 20 to 700.


The EVA has a MI within a range of about 20 to about 2300. The EVA has a vinyl acetate concentration ranging from about 10% to about 30% by weight.


The present invention further includes a kit for image transfer. The kit comprises an image transfer sheet that is comprised of a substrate layer, a release layer and an image imparting layer made of a polymer such as LDPE, EAA, EVA, or MAEA or mixtures of these polymers that melt at a temperature within a range of about 100 degrees C. to about 700 degrees C. The LDPE has a melt index of about 60 to about 1,200 (SI)-g/minute. The kit can also include a device for imparting an image-imparting medium to the polymer component of the image imparting layer of the image transfer sheet. One kit embodiment additionally includes an image receiving substrate, such as an ink receptive layer, that is an element of the image transfer sheet.


DETAILED DESCRIPTION

In one embodiment of the present invention, an image transfer sheet, illustrated generally at 10 in FIG. 1, is comprised of a substrate layer 12, a release layer 14 comprising a silicone coating and a peel layer 16 that together have a thickness of about 3 to 8 mils. The peel layer 16 can also be referred to as an image imparting layer 16, and can comprise a polymer component selected from one or more of a low density polyethylene (LDPE), ethylene acrylic acid (EAA), ethylene vinyl acetate (EVA), or methane acrylic ethylene acetate (M/EAA), having a melt index of about 20 to about 1200 (SI) g/10 minute and a polymer thickness of about 0.7 to about 2.3 mils of polymer or (20 g/m2 to 50 g/m2 with a melting point range of 40 degrees C. to 450 degrees C.). The release layer 14 is sandwiched between the substrate layer 12 and the peel layer 16 comprising a polymeric material such as LDPE, EAA, EVA or M/EAA.


Another embodiment of the present invention also includes a method for transferring an image from one substrate to another. The method comprises a step of providing or obtaining an image transfer sheet 10 that is comprised of a substrate or base layer 12, such as box paper with a base weight of 75 g/m2 to 162 g/m2, a release layer 14, comprising a silicone coating, and a peel layer 16 that includes one or more of the polymers LDPE, EAA, EVA, or M/EAA at a thickness of about 1.5 mils and having a melt index, MI, within a range of 60 degrees C. to 1300 degrees C. Next, an image is imparted to the polymer component of the peel layer 16 utilizing a top coating image-imparting material such as ink or toner. The ink or toner may be applied utilizing any conventional method such as an ink jet printer or an ink pen or color copy or a laser printer. The ink may be comprised of any conventional ink formulation. An ink jet coating is preferred.


The image transfer sheet 10 is, in one embodiment, applied to a second substrate, also called the image receiving substrate, so that the polymeric component of the peel layer 16 contacts the second substrate. The second substrate may be comprised of materials such as cloth, paper and other flexible or inflexible materials. Once the image transfer sheet 10 contacts the second substrate, a source of heat, such as an iron or other heat source, is applied to the image transfer sheet 10 and heat is transferred through the substrate 12 and the release layer 14 to the peel layer 16. The peel layer 16 transfers the image to the second substrate. The application of heat to the transfer sheet 10 results in ink or other image-imparting media within the polymeric component of the peel layer being changed in form to particles encapsulated by the polymeric substrate such as the LDPE, EAA, EVA or M/EAA immediately proximal to the ink or toner. The encapsulated ink particles or encapsulated toner particles are then transferred to the second substrate in a minor image to the ink image or toner image on the polymeric component of the peel layer while the portion of the polymer of the peel layer 16 not contacting the ink or toner and encapsulating the ink or toner is retained on the image transfer sheet 10.


When image imparting media and techniques such as color copy, laser techniques, toner or thermo transfer from ribbon wax or resin are employed, it is not necessary to apply an image receiving layer to the image transfer sheet.


As used herein, the term “melt index” refers to the value obtained by performing ASTM D-1238 under conditions of temperature, applied load, timing interval and other operative variables which are specified therein for the particular polymer being tested.


It is believed that the addition of ink or toner to the image imparting layer, specifically, to the LDPE or to the EAA, EVA, or E/MAA polymeric component, locally lowers the melting point of the polymeric component material such as LDPE, EAA, EVA, or E/MAA which either contacts the ink or toner or is immediately adjacent to the ink or toner. Thus, an application of heat to the polymeric component of the peel layer 16 results in a change in viscosity of the low density polyethylene or other polymeric material contacted by the ink or toner and immediately adjacent to the ink or toner as compared to the surrounding polymeric media. It is believed that the polymeric component such as LDPE, EAA, EVA or E/MAA polyethylene locally melts with the ink or toner. However, as heat is removed and the area cools, the polymeric component solidifies and encapsulates the ink or toner. The solidification-encapsulation occurs substantially concurrently with transfer of the ink-LDPE or ink-EAA, ink-EVA or ink-E/MAA or other polymer mixture to the receiving substrate.


Because the polymeric component of the peel layer 16 generally has a high melting point, the application of heat, such as from an iron, does not result in melting of this layer or in a significant change in viscosity of the overall peel layer 16. The change in viscosity is confined to the polymeric component that actually contacts the ink or toner or is immediately adjacent to the ink or toner. As a consequence, a mixture of the polymeric component and ink or toner is transferred to the second substrate sheet as an encapsulate whereby the polymeric component encapsulates the ink or toner. It is believed that the image transfer sheet of the present invention is uniquely capable of both cold peel and hot peel with a very good performance for both types of peels.


One polymeric component, the low density polyethylene ethylene-acrylic acid (EAA) polymeric component, is formed as a product of the co-polymerization of ethylene and acrylic acid forming a polymer with carboxyl groups. The low density EAA polymer is more amorphous than low density polyethylene which causes the EAA to decrease in melting point as compared to LDPE. The carboxyl groups of the acrylic acid group of EAA also provide chemical functional groups for hydrogen bonding.


In one preferred EAA polymer embodiment, acrylic acids are present in a concentration of 5% to 25% by weight of the EAA formulation. The EAA has a melt index ranging from 20 to 1200. The most preferred EAA formulation has an acrylic acid concentration of 10% to 20% by weight. This EAA embodiment has a MI of 60 to 500.


Other polymeric materials that may be used include an ethylene melt with acrylic acid copolymer resin and with a melt flow index ranging from 20 to 1,500 DS/minute and preferably having a melt flow index of 50 to 100 DS/minute. This ethylene-acrylic acid polymer melt, known as E/MAA, along with ethylene acrylic acid, EAA, or ethylene vinyl acetate (EVA) with acetate percentages ranging from 4% to 30% and preferably 11% to 20% may be used as the polymer in the peel layer 16. One other preferred E/MAA embodiment has a MI of 60 to 600. One preferred embodiment of E/MAA and EAA includes an acid content within a concentration range of 4% to 25%.


One other polymeric material that may be used is EVA with Vinyl Acetate contents. This polymer has a MI of 100 to 2300. The vinyl acetate contents range from approximately 10% to 30% by weight. In one preferred embodiment, the EVA includes vinyl acetate contents of 10% to 28%, with a melt index within a range of 10 to 600. In one other preferred embodiment, the EVA has an MI within a range of 20 to 600. It is also contemplated that a polyethylene copolymer dispersion may be suitable for use in this layer.


The melt flow indices of these polymer components range from 100 DS/minute to 2,500 DS/minute with a preferable range of 20 to 700 DS/minute. Each of these polymeric components, in addition to a Surlyninoma resin are usable with or without additives, such as slip additives, UV absorbents, optical brighteners, pigments, antistatics and other additives conventionally added to this type of polymer. All of these polymeric components have softening points within a range of 40 degrees C. to 300 degrees C.


The sheet and method of the present invention accomplish with a simple elegance what other methods and transfer sheets have attempted to accomplish with a great deal of complexity. The sheet and method of the present invention do not require complicated coloring or image-generating systems such as preformed encapsulates. The image transfer sheet and method, furthermore, do not require complicated layer interaction in order to transfer a stable image to an image receiving substrate. The image transfer sheet of the present invention merely requires a user to impart an image to the polymeric component of the peel or image imparting layer with a material such as ink or toner. In one embodiment, once the image is transferred, the user contacts the peel layer 16 to the second or receiving substrate and applies a source of heat such as an iron. The capacity of the polymeric component of the peel layer to encapsulate an image-imparting media such as ink or toner renders this image transfer sheet exceedingly versatile.


The substrate layer 12 of the image transfer sheet 10 is preferably made of paper but may be made of any flexible or inflexible material ranging from fabric to polypropylene. Specific substrate materials include polyester film, polypropylene, or other film having a matte or glossy finish. In one embodiment, the substrate is a base paper having a weight-to-surface area within a range of 60 g/m2 to 245 g/m2 and preferably a range of 80 g/m2 to 145 g/m2. The substrate has a thickness that falls within a range of 2.2 to 12.0 mils and a preferred thickness of 3 to 8.0 mils, as measured in a Tappi 411 test procedure.


The substrate layer may be coated with clay on one side or both sides. The substrate layer may be resin coated or may be free of coating if the substrate is smooth enough. In one embodiment, overlying the substrate is a silicone coating. The silicone coating has a range of thickness of 0.1 to 2.0 mils with a preferred thickness range of 0.1 to 0.7 mils. The silicone coating has a release in g/inch within a range of 50 to 1100 and a preferred release of 65 to 800 g/inch as measured by a Tappi-410 method. Other release coatings such as fluorocarbon, urethane, or acrylic base polymer may be used.


The silicone-coated layer acts as a release-enhancing layer. It is believed that when heat is applied to the image transfer sheet, thereby encapsulating the image-imparting media such as ink or toner with low density polyethylene, Ethylene Acrylic Acid (EAA), Ethylene Vinyl Acetate (EVA) or Methane Acrylic Ethylene Acrylic (MAEA), or mixtures of these materials, local changes in temperature and fluidity of the low density polyethylene or other polymeric material occurs. These local changes are transmitted into the silicone-coated release layer and result in local, preferential release of the low density polyethylene encapsulates.


This local release facilitates transfer of a “clean” image from the image transfer sheet to the final substrate. By “clean” image is meant an image with a smooth definition.


The silicone-coated release layer is an optional layer that may be eliminated if the image receiving surface 17 of the peel layer 16 is sufficiently smooth to receive the image. In instances where a silicone-coated release layer is employed, a silicone-coated paper with silicone deposited at 0.32 to 2.43 g/m2 is employed. The silicone-coated paper preferably has a release value between 50 g/in. and 700 g/in. The paper may be coated on a backside for curl control or other function, printability or heat stabilities.


A top surface of the silicone may be treated with a corona treatment or chemical treatment prior to application of the polymeric component or on top of the polymer in order to provide better adhesion or to improve washability of the image transferred.


One desirable quality of the polymeric component, LDPE, EVA, EAA or M/EAA, is that it has a capacity to coat any fibers or other types of discontinuities on the image receiving substrate and to solidify about these fibers or discontinuities. This coating and solidification on fibers or any other type of discontinuity in the receiving substrate aids in imparting a permanency to the final, transferred image. Because the image-generated media, such as ink or toner, is actually encapsulated in the low density polyethylene or other polymeric component material, the image transferred along with the LDPE, EVA, EAA or M/EAA, is a permanent image that cannot be washed away or removed with conventional physical or chemical perturbations such as machine washing. The polymeric materials LDPE, EVA, EAA, or M/EAA are relatively inert to chemical perturbations. In one embodiment, the LDPE, EVA, EAA, or M/EAA is applied to either the substrate or the release layer 14 in a thickness within a range of 0.5 mils to 2.8 mils or 10 g/m2 to 55 g/m2 and preferably 22 g/m2 to 48 g/m2.


Overlying the polymeric component containing peel layer 16 can be a prime layer GAT with polyethylene dispersion or an EAA or EVA dispersion. This layer can have a high melting index within a range of 200 to 2,000. The EAA emulsion dispersion has an MI of 200 to 2000 and has an acrylic acid concentration of 7% to 25% by weight. The EVA dispersion has an MI of 200 to 2500 and an acetate or other acrylic polymer concentration of 7% to 33% by weight.


A fifth layer can be an ink jet coating receptor layer having a thickness of 3 g/m2 to 30 g/m2. Overlying the ink jet coating receptor layer can be an ink jet top coating layer having a thickness of 4 g/m2 to 30 g/m2. In one embodiment, the ink jet coating receptor layer and ink jet top coating layer are combined to create a single layer having a heavier coat weight. This layer is not required when image imparting techniques such as color copy, laser, toner, or thermo transfer from ribbon wax or resin are employed.


In one embodiment, the image transfer sheet of the present invention is made by applying a low density polyethylene, or a low density polyethylene ethylene acrylic acid or an ethylene vinyl acetate (10% to 28%) of vinyl acetate to the substrate utilizing a process such as extrusion, hot melt, slot die, or a “roll on” process or other similar process.


The low density polyethylene preferably has a melt index within a range of 20 to 1,200 g/10 minutes and most preferably a melt index of 100 to 700-g/minute. An acceptable melt flow rate measured at 125 degrees C. and 325 grams falls within a range of 7 to 30 g/10 min., with a preferred range of 8 to 20 g/10 min., as measured by ASTM Test Method D-1238. An Equivalent Melt Index, EMI, which is equal to 66.8 times (Melt Flow Rate at 125 degrees C., 325 grams) 0.83, may acceptably range from 30 to 2000 g/10 min., and preferably ranges from 200 to 800 g/10 min. The Melting Point, Tm, ranges from 43 degrees C. to 250 degrees C. with a preferred range of 65 degrees C. to 150 degrees C. as measured in ASTM Test Method D-3417. The Vicat Softening Point of the LDPE ranges from 43 degrees C. to 150 degrees C. as measured by ASTM Test Method D-1525.


The ethylene vinyl acetate (EVA) has a melt index of 200 to 2500 dg/minute with a preferred index range of 200 to 1200 dg/min. The Ring and Ball Softening Point ranges from 67 degrees C. to 200 degrees C., with a preferred range of 76 degrees C. to 150 degrees C. The percent vinyl acetate in the EVA is within a range of 5% to 33% and preferably within a range of 10% to 33%. The metoacrylic acid or ethylene acrylic acid also known as Nucryl™ has a concentration of about 4% to 20% acrylic acid and a melt index within a range of 50 to 1,300-g/minute. The preferable range is 200 to 600-g/minute.


The EAA/EMAA has a Melt Index of 20 to 1300 dg/min., with a preferred range of 60 to 700 dg/min., as measured in ASTM Test Method D-1238. The Vicat Softening Point ranges from 43 degrees C. to 225 degrees C., with a preferred range of 43 degrees C. to 150 degrees C., as measured by ASTM Test 43 degrees C. to 150 degrees C. The EAA/EMAA has a percent acrylic acid concentration within a range of 5% to 25%, with a preferred range of 7% to 22% by weight. The Melt Flow Rate ranges from 7 to 90 g/10 min., with a preferred range of 7 to 65 g/10 min., as measured by ASTM test method D-1238.


Twenty-eight g/m2 to 50 g/m2 can be applied to a substrate. The application thickness of one of the LDPE, EAA, EVA or Nucryl™ is 1 to 2 mils in thickness. The most preferred range of thickness of 1.0 to 2.2 mils.


In one embodiment, the polymeric components of LDPE, EAA, EVA or Nucryl™ is applied to a silicone-release coated paper. The silicone-release coating is applied to paper or film to basis WT 80 g/m2 an application quantity of 80 g/m2 to 200 g/m2 and preferably at a rate of 95 g/m2 to 170 g/m2.


Application of the polymeric component to the substrate, such as release coated paper, may be by extrusion, roll coater, any coating process, slot-die or hot melt extrusion. Other acceptable methods of application include an air knife or rod blade application. The polymeric component may be prime coated with a corona treatment or chemical treatment with acrylic acid emulsion having a melt index of 300 to 2,000-g/min., or an EVA emulsion, chemical primer or corona treatment or may be eliminated if chemical treatment for adhesion was applied. A top coat may be applied over the polymeric component. The final application is an ink jet coating of two or three passes to deposit 4 g/m2 to 30 g/m2 depending on particular printing applications.


One embodiment of the image transfer sheet is described in Table 1 with respect to layer identity, interlayer relationship and rate of application of each layer.











TABLE 1








Layer Type
Applications (in g/m2, unless




otherwise indicated)



Base paper
70 to 160 (layer barrier coating 3 to




10 applied on one or both sides of




the base paper)



Silicone coating (or other
0.4 to 2 lbs/3000 SF



release coating)




Corona treatment (may or




may not be necessary)




Film or peel layer
20 to 50



Corona treatment (or other
 1 to 5



chemical treatment)




Ink jet coating
 4 to 35 (the ink jet coating could




be applied in one, two, three or




additional passes)









The film layer may be applied as a cold peel or as a hot peel.


Presented herein is an example of one preferred embodiment of the image transfer sheet of the present invention. This example is presented to illustrate particular layers and particular specification for the layers and is not intended to limit the scope of the present invention.


EXAMPLE

In one embodiment, the image transfer sheet included a first substrate layer of base paper having a basis weight of 65 g/m2 to 145 g/m2 and preferably falling within a range of 97 g/m2 to 138 g/m2. While paper is described, it is contemplated that materials such as polyester film, polypropylene or polyethylene or other film of 142 to 1,000 gauge matte or glossy finish may be employed. In instances where paper is used, the paper may be clay coated on one side or both sides, or polymer coated.


Overlaying the base substrate paper layer was a release layer comprising silicone. Other acceptable release coatings include fluorocarbon or other acrylic, urethane release coatings and so on. The release layer had a release value ranging from 50 g/in. to 2,000 g/in., and preferably a range of 80 g/in. to 500 g/in. The release layer may be omitted if the base paper has a surface of sufficient smoothness.


A third layer, which is a peel layer of the image transfer sheet, includes a low density polyethylene or other polymer polyethylene applied at a thickness of 0.5 mils to 2.8 mils or 10 g/m2 to 55 g/m2 and preferably 22 g/m2 to 48 g/m2. Other acceptable materials for use in the third layer include acrylic acid of 5% to 22% ethylene vinyl acetate, 10% to 28% (EVA) with a melt index ranging from 30 to 2,000. In one preferred embodiment, the melt index was 60 to 500. In addition to the materials mentioned, the third layer may also be comprised of a polyethylene copolymer dispersion.


The LDPE or EVA or polyethylene copolymer dispersion is primed with GAT with a high melt index ranging from 200 to 2,000. A preferred range is 200 to 2,000. It is contemplated that this primer layer is optional.


A fifth layer is a first layer of ink jet coating receptor laid down in a concentration of 3 g/m2 to 30 g/m2.


A sixth layer which is a third ink jet top coating is laid down at a concentration of 4 g/m2 to 15 g/m2. It is possible that the ink jet top coating could be laid down in a single pass in order to make a single layer with a heavier coat weight.


The above Detailed Description includes references to the accompanying drawing, which forms a part of the Detailed Description. The drawing shows, by way of illustration, a specific embodiment in which the present image transfer sheets, method and kits can be practiced.


The above description is intended to be illustrative, and not restrictive. For example, the above-described embodiments and examples can be used in combination with each other. Other embodiments can be used, such as by one of ordinary skill in the art upon reviewing the above description. Also, in the above Detailed Description, various features can be grouped together to streamline the disclosure. This should not be interpreted as intending that an unclaimed disclosed feature is essential to any claim. Rather, inventive subject matter can lie in less than all features of a particular disclosed embodiment. Thus, the following claims are hereby incorporated into the Detailed Description, with each claim standing on its own as a separate embodiment. The scope of the invention should be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.


In the appended claims, the terms “including” and “in which” are used as the plain-English equivalents of the respective terms “comprising” and “wherein.” Also, in the following claims, the terms “including” and “comprising” are open-ended, that is, an assembly, assembly, device, article, kit, or process that includes elements in addition to those listed after such a term in a claim are still deemed to fall within the scope of that claim. Moreover, in the following claims, the terms “first,” “second,” and “third,” etc. are used merely as labels, and are not intended to impose numerical requirements on their objects.


The Abstract is provided to comply with 37 C.F.R. §1.72(b), to allow the reader to quickly ascertain the nature of the technical disclosure. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims.

Claims
  • 1. An image transfer article, comprising: a removable substrate including a first and a second substrate surface, the first substrate surface abutting a release-enhancing coating; anda peel member overlaying, and peelable from, the release-enhancing coating, the peel member including a polymer component configured to carry image indicia to be transferred,wherein a local melting point of the polymer component that is contacted by, or immediately adjacent to, the image indicia is reduced relative to the remaining portions of the polymer component.
  • 2. The image transfer article of claim 1, wherein a surface of the release-enhancing coating abutting the peel member is one or both of corona treated or chemically treated prior to being overlaid with the peel member.
  • 3. The image transfer article of claim 1, wherein the release-enhancing coating includes silicone.
  • 4. The image transfer article of claim 1, wherein the release-enhancing coating has a thickness ranging from about 0.1 mils to about 2 mils, inclusive.
  • 5. The image transfer article of claim 1, wherein the polymer component has a thickness ranging from about 0.5 mils to about 2.8 mils, inclusive, and is configured to receive image-imparting media forming the image indicia from a copying or printing process.
  • 6. The image transfer article of claim 1, wherein the polymer component includes at least one of low density polyethylene, ethylene vinyl acetate, a copolymer of ethylene and acrylic acid, or ethylene acrylic acid.
  • 7. The image transfer article of claim 6, wherein the polymer component includes ethylene acrylic acid having an acrylic acid concentration within a range of 10% to 20% by weight, inclusive, or having a melt index within a range of 60 to 500, inclusive.
  • 8. The image transfer article of claim 1, further comprising an image-receptive member overlaying the peel member and configured to receive image-imparting media forming the image indicia from a copying or printing process.
  • 9. An image transfer article, comprising: a removable substrate including a first and a second substrate surface, the first substrate surface abutting a release-enhancing coating; anda peel member overlaying, and peelable from, the release-enhancing coating, the peel member including a polymer component configured to carry image indicia to be transferred,wherein the polymer component is configured to encapsulate the image indicia and coat discontinuities of an image receiving substrate when heat is applied to the polymer component, the polymer component further configured to solidify about the discontinuities when the application of heat is discontinued.
  • 10. The image transfer article of claim 9, wherein the discontinuities include fibers of the image receiving substrate.
  • 11. The image transfer article of claim 9, wherein a surface of the release-enhancing coating abutting the peel member is one or both of corona treated or chemically treated prior to being overlaid with the peel member.
  • 12. The image transfer article of claim 9, wherein the polymer component has a thickness ranging from about 0.5 mils to about 2.8 mils, inclusive, and is configured to receive image-imparting media forming the image indicia from a copying or printing process.
  • 13. The image transfer article of claim 9, wherein the polymer component includes at least one of low density polyethylene, ethylene vinyl acetate, a copolymer of ethylene and acrylic acid, or ethylene acrylic acid.
  • 14. The image transfer article of claim 9, further comprising an image-receptive member overlaying the peel member and configured to receive image-imparting media forming the image indicia from a copying or printing process.
  • 15. An assembly, comprising: an image transfer article, comprising: a removable substrate including a first and a second substrate surface, the first substrate surface abutting a release-enhancing coating;a peel member overlaying, and peelable from, the release-enhancing coating, the peel member including a polymer component; andimage indicia imparted to the polymer component; andan image receiving substrate contactable with the peel member;wherein the polymer component is configured to encapsulate the image indicia when heat is applied, and the encapsulated image indicia is bondable to the image receiving substrate, andwherein a local melting point of the polymer component that is contacted by, or immediately adjacent to, the image indicia is reduced relative to the remaining portions of the polymer component.
  • 16. The assembly of claim 15, wherein the release-enhancing coating includes silicone.
  • 17. The assembly of claim 15, wherein the release-enhancing coating has a thickness ranging from about 0.1 mils to about 2 mils, inclusive, thereby allowing sufficient heat to reach the peel member for encapsulating the image indicia on the image receiving substrate.
  • 18. The assembly of claim 15, wherein the polymer component has a thickness ranging from about 0.5 mils to about 2.8 mils, inclusive, and is configured to receive image-imparting media forming the image indicia from a copying or printing process.
  • 19. The assembly of claim 15, wherein the polymer component includes at least one of low density polyethylene, ethylene vinyl acetate, a copolymer of ethylene and acrylic acid, or ethylene acrylic acid.
  • 20. The assembly of claim 15, wherein the image receiving substrate is a light-colored fabric.
RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 12/955,512 filed Nov. 29, 2010, now allowed, which is a continuation of U.S. application Ser. No. 11/054,717 filed Feb. 9, 2005, now U.S. Pat. No. RE 42,541, which is a reissue of U.S. application Ser. No. 09/150,983 filed Sep. 10, 1998, now U.S. Pat. No. 6,551,692, the entirety of each of the disclosures of which are explicitly incorporated by reference herein. This application is also related to U.S. application Ser. No. 09/535,937 filed Mar. 24, 2000, now U.S. Pat. No. 6,497,781, the entirety of which is explicitly incorporated by reference herein.

US Referenced Citations (156)
Number Name Date Kind
3790439 La Perre et al. Feb 1974 A
3922435 Asnes Nov 1975 A
4102456 Morris Jul 1978 A
4169169 Kitabatake Sep 1979 A
4224358 Hare Sep 1980 A
4235657 Greenman et al. Nov 1980 A
4284456 Hare Aug 1981 A
4399209 Sanders et al. Aug 1983 A
4461793 Blok et al. Jul 1984 A
4548857 Galante Oct 1985 A
4549824 Sachdev et al. Oct 1985 A
4594276 Relyea Jun 1986 A
4685984 Powers et al. Aug 1987 A
4758952 Harris, Jr. et al. Jul 1988 A
4863781 Kronzer Sep 1989 A
4880678 Goffi Nov 1989 A
4966815 Hare Oct 1990 A
4980224 Hare Dec 1990 A
5019475 Higashiyama et al. May 1991 A
5028028 Yamada et al. Jul 1991 A
5045383 Maeda et al. Sep 1991 A
5059580 Shibata et al. Oct 1991 A
5097861 Hopkins et al. Mar 1992 A
5110389 Hiyoshi et al. May 1992 A
5133819 Croner Jul 1992 A
5139917 Hare Aug 1992 A
5217793 Yamane et al. Jun 1993 A
5236801 Hare Aug 1993 A
5242739 Kronzer et al. Sep 1993 A
5252531 Yasuda et al. Oct 1993 A
5271990 Kronzer et al. Dec 1993 A
5320885 Yamane et al. Jun 1994 A
5334439 Kawaguchi et al. Aug 1994 A
5350474 Yamane Sep 1994 A
5362703 Kawasaki et al. Nov 1994 A
5372884 Abe et al. Dec 1994 A
5400246 Wilson et al. Mar 1995 A
5407724 Mimura et al. Apr 1995 A
5431501 Hale et al. Jul 1995 A
5434598 Shimomine et al. Jul 1995 A
5501902 Kronzer Mar 1996 A
5521229 Lu et al. May 1996 A
5614345 Gumbiowski et al. Mar 1997 A
5620548 Hare Apr 1997 A
5665476 Oez Sep 1997 A
5707925 Akada et al. Jan 1998 A
5770268 Kuo et al. Jun 1998 A
5798161 Kita et al. Aug 1998 A
5798179 Kronzer Aug 1998 A
5821028 Maejima et al. Oct 1998 A
5833790 Hare Nov 1998 A
5861355 Olson et al. Jan 1999 A
5905497 Vaughan et al. May 1999 A
5917730 Rittie et al. Jun 1999 A
5925712 Kronzer Jul 1999 A
5942335 Chen et al. Aug 1999 A
5948586 Hare Sep 1999 A
5962149 Kronzer Oct 1999 A
5981045 Kuwabara et al. Nov 1999 A
5981077 Taniguchi Nov 1999 A
6017611 Cheng et al. Jan 2000 A
6033739 Kronzer Mar 2000 A
6033824 Hare et al. Mar 2000 A
6036808 Shaw-Klein et al. Mar 2000 A
6042914 Lubar Mar 2000 A
6054223 Tsuchiya et al. Apr 2000 A
6066387 Ueda et al. May 2000 A
6071368 Boyd et al. Jun 2000 A
6083656 Hare et al. Jul 2000 A
6087061 Hare et al. Jul 2000 A
6090520 Hare et al. Jul 2000 A
6096475 Hare et al. Aug 2000 A
6106982 Mientus et al. Aug 2000 A
6113725 Kronzer Sep 2000 A
6120888 Dolsey et al. Sep 2000 A
6139672 Sato et al. Oct 2000 A
6177187 Niemoller et al. Jan 2001 B1
6180256 Sargeant Jan 2001 B1
6200668 Kronzer Mar 2001 B1
6242082 Mukoyoshi et al. Jun 2001 B1
6245710 Hare Jun 2001 B1
6258448 Hare Jul 2001 B1
6265128 Hare et al. Jul 2001 B1
6294307 Hare Sep 2001 B1
6331374 Hare et al. Dec 2001 B1
6338932 Hare et al. Jan 2002 B2
6340550 Hare et al. Jan 2002 B2
6358660 Agler et al. Mar 2002 B1
6383710 Hare et al. May 2002 B2
6423466 Hare Jul 2002 B2
6428878 Kronzer Aug 2002 B1
6450633 Kronzer Sep 2002 B1
6495241 Sato et al. Dec 2002 B2
6497781 Dalvey et al. Dec 2002 B1
6506445 Popat et al. Jan 2003 B2
6509131 Hare et al. Jan 2003 B2
6521327 Franke Feb 2003 B1
6531216 Williams et al. Mar 2003 B1
6539652 Barry Apr 2003 B1
6551692 Dalvey et al. Apr 2003 B1
6582803 Cole et al. Jun 2003 B2
6638604 Bamberg et al. Oct 2003 B1
6638682 Hare et al. Oct 2003 B2
6667093 Yuan et al. Dec 2003 B2
6677009 Boyd et al. Jan 2004 B2
6703086 Kronzer et al. Mar 2004 B2
6723773 Williams et al. Apr 2004 B2
6753050 Dalvey et al. Jun 2004 B1
6786994 Williams et al. Sep 2004 B2
6849312 Williams Feb 2005 B1
6869910 Williams et al. Mar 2005 B2
6871950 Higuma et al. Mar 2005 B2
6875487 Williams et al. Apr 2005 B1
6878423 Nakanishi Apr 2005 B2
6884311 Dalvey et al. Apr 2005 B1
6916589 Hare et al. Jul 2005 B2
6916751 Kronzer Jul 2005 B1
6951671 Mukherjee et al. Oct 2005 B2
6998211 Riley et al. Feb 2006 B2
7001649 Wagner et al. Feb 2006 B2
7008746 Williams et al. Mar 2006 B2
7021666 Hare Apr 2006 B2
7022385 Nasser Apr 2006 B1
7026024 Chang et al. Apr 2006 B2
7081324 Hare et al. Jul 2006 B1
7160411 Williams et al. Jan 2007 B2
7220705 Hare May 2007 B2
7238410 Kronzer Jul 2007 B2
7361247 Kronzer Apr 2008 B2
7364636 Kronzer Apr 2008 B2
7749581 Dalvey et al. Jul 2010 B2
7754042 Dalvey et al. Jul 2010 B2
7766475 Dalvey et al. Aug 2010 B2
7771554 Dalvey et al. Aug 2010 B2
RE41623 Schwendimann et al. Sep 2010 E
7824748 Dalvey et al. Nov 2010 B2
RE42541 Dalvey et al. Jul 2011 E
20010051265 Williams et al. Dec 2001 A1
20020025208 Sato et al. Feb 2002 A1
20020048656 Sato et al. Apr 2002 A1
20020192434 Yuan et al. Dec 2002 A1
20030008112 Cole et al. Jan 2003 A1
20030021962 Mukherjee et al. Jan 2003 A1
20040100546 Horvarth May 2004 A1
20040146700 Boyd et al. Jul 2004 A1
20050048230 Dalvey et al. Mar 2005 A1
20070172609 Williams Jul 2007 A1
20070172610 Williams Jul 2007 A1
20070221317 Kronzer et al. Sep 2007 A1
20070231509 Xu et al. Oct 2007 A1
20080149263 Dalvey et al. Jun 2008 A1
20080302473 Dalvey et al. Dec 2008 A1
20080305253 Dalvey et al. Dec 2008 A1
20080305288 Dalvey et al. Dec 2008 A1
20100323132 Dalvey et al. Dec 2010 A1
20110067806 Dalvey et al. Mar 2011 A1
Foreign Referenced Citations (11)
Number Date Country
0466503 Jan 1992 EP
0782931 Jul 1997 EP
0881092 Dec 1998 EP
0899121 Mar 1999 EP
0933225 Aug 1999 EP
2295973 Jun 1996 GB
63122592 May 1988 JP
1037233 Feb 1989 JP
7276833 Oct 1995 JP
8085269 Apr 1996 JP
WO-0073570 Dec 2000 WO
Non-Patent Literature Citations (131)
Entry
U.S. Appl. No. 12/875,445, filed Sep. 3, 2010, Image Transfer on a Colored Base.
“U.S. Appl. No. 09/150,983, Final Office Action mailed Aug. 2, 2000”, 9 pgs.
“U.S. Appl. No. 09/150,983, Non-Final Office Action mailed Jan. 30, 2001”, 7 pgs.
“U.S. Appl. No. 09/150,983, Non-Final Office Action mailed Apr. 11, 2000”, 5 pgs.
“U.S. Appl. No. 09/150,983, Non-Final Office Action mailed Dec. 28, 1999”, 5 pgs.
“U.S. Appl. No. 09/150,983, Notice of Allowance mailed Nov. 19, 2002”, 8 pgs.
“U.S. Appl. No. 09/150,983, Response filed Feb. 16, 2000 to Non-Final Office Action Dec. 28, 1999”, 3 pgs.
“U.S. Appl. No. 09/150,983, Response filed Jun. 20, 2000 to Non-Final Office Action mailed Apr. 11, 2000”, 7 pgs.
“U.S. Appl. No. 09/150,983, Response filed Aug. 7, 2002 to Non-Final Office Action filed Jan. 30, 2001”, 9 pgs.
“U.S. Appl. No. 09/391,910, Restriction Requirement mailed Jun. 18, 2001”, 5 pgs.
“U.S. Appl. No. 09/535,937, Non-Final Office Action mailed Nov. 29, 2001”, 8 pgs.
“U.S. Appl. No. 09/535,937, Notice of Allowance mailed Sep. 10, 2002”, 9 pgs.
“U.S. Appl. No. 09/535,937, Preliminary Amendment mailed Mar. 24, 2000”, 1 pg.
“U.S. Appl. No. 09/535,937, Response filed May 28, 2002 to Non-Final Office Action mailed Nov. 29, 2001”, 6 pgs.
“U.S. Appl. No. 09/541,845, Final Office Action mailed Nov. 25, 2003”, 4 pgs.
“U.S. Appl. No. 09/541,845, Non-Final Office Action mailed Apr. 16, 2003”, 4 pgs.
“U.S. Appl. No. 09/541,845, Notice of Allowance mailed May 4, 2004”, 4 pgs.
“U.S. Appl. No. 09/541,845, Response filed Jan. 10, 2003 to Restriction Requirementmailed Aug. 22, 2002”, 1 pg.
“U.S. Appl. No. 09/541,845, Response filed Mar. 23, 2004 to Final Office Action mailed Nov. 25, 2003”, 6 pgs.
“U.S. Appl. No. 09/541,845, Response filed Jul. 15, 2003 to Non-Final Office Action mailed Apr. 14, 2003”, 5 pgs.
“U.S. Appl. No. 09/541,845, Restriction Requirement mailed Aug. 22, 2002”, 5 pgs.
“U.S. Appl. No. 09/541,845, Supplemental Notice of Allowability mailed Jan. 26, 2005”, 2 pgs.
“U.S. Appl. No. 09/541,845, Supplemental Restriction Requirement mailed Jan. 6, 2003”, 5 pgs.
“U.S. Appl. No. 09/661,532, Final Office Action mailed May 20, 2003”, 8 pgs.
“U.S. Appl. No. 09/661,532, Non-Final Office Action mailed Mar. 1, 2002”, 9 pgs.
“U.S. Appl. No. 09/661,532, Notice of Allowance mailed Feb. 12, 2004”, 4 pgs.
“U.S. Appl. No. 09/661,532, Response filed Aug. 20, 2003 to Final Office Action mailed May 20, 2003”, 5 pgs.
“U.S. Appl. No. 09/661,532, Response filed Aug. 30, 2002 to Non-Final Office Action mailed Mar. 1, 2002”, 8 pgs.
“U.S. Appl. No. 09/661,532, Response filed Dec. 23, 2002 to Restriction Requirement mailed Nov. 26, 2002”, 2 pgs.
“U.S. Appl. No. 09/661,532, Restriction Requirement mailed Nov. 26, 2002”, 5 pgs.
“U.S. Appl. No. 10/719,220, Non-Final Office Action mailed Sep. 9, 2004”, 3 pgs.
“U.S. Appl. No. 10/719,220, Preliminary Amendment filed Nov. 21, 2003”, 3 pgs.
“U.S. Appl. No. 10/911,249, Examiner Interview Summary mailed Jan. 15, 2010”, 4 pgs.
“U.S. Appl. No. 10/911,249, Final Office Action filed Jul. 26, 2005”, 3 pgs.
“U.S. Appl. No. 10/911,249, Final Office Action filed Dec. 8, 2006”, 3 pgs.
“U.S. Appl. No. 10/911,249, Final Office Action filed Dec. 14, 2006”, 3 pgs.
“U.S. Appl. No. 10/911,249, Final Office Action mailed Jun. 30, 2009”, 5 pgs.
“U.S. Appl. No. 10/911,249, Final Office Action mailed Jan. 29, 2008”, 6 pgs.
“U.S. Appl. No. 10/911,249, Non-Final Office Action filed Feb. 8, 2005”, 5 pgs.
“U.S. Appl. No. 10/911,249, Non-Final Office Action filed Mar. 13, 2007”, 4 pgs.
“U.S. Appl. No. 10/911,249, Non-Final Office Action mailed Mar. 16, 2010”, 6 pgs.
“U.S. Appl. No. 10/911,249, Non-Final Office Action mailed Sep. 20, 2007”, 5 pgs.
“U.S. Appl. No. 10/911,249, Notice of Allowance mailed Mar. 25, 2008”, 4 pgs.
“U.S. Appl. No. 10/911,249, Notice of Allowance mailed Aug. 20, 2010”, 16 pgs.
“U.S. Appl. No. 10/911,249, Preliminary Amendment mailed Aug. 4, 2004”, 4 pgs.
“U.S. Appl. No. 10/911,249, Response filed Jan. 5, 2009 to Final Office Action mailed Dec. 5, 2008”, 10 pgs.
“U.S. Appl. No. 10/911,249, Response filed Jan. 24, 2007 to Non Final Office Action mailed Dec. 14, 2006”, 8 pgs.
“U.S. Appl. No. 10/911,249, Response filed Jan. 26, 2006 to Final Office Action filed Jul. 26, 2005”, 7 pgs.
“U.S. Appl. No. 10/911,249, Response filed Feb. 18, 2008 to Final Office Action filed Jan. 29, 2008”, 7 pgs.
“U.S. Appl. No. 10/911,249, Response filed Mar. 11, 2009 to Final Office Action mailed Feb. 9, 2009”, 13 pgs.
“U.S. Appl. No. 10/911,249, Response filed May 4, 2005 to Non-Final Office Action filed Feb. 8, 2005”, 6 pgs.
“U.S. Appl. No. 10/911,249, Response filed Jun. 7, 2010 to Non Final Office Action mailed Mar. 16, 2010”, 14 pgs.
“U.S. Appl. No. 10/911,249, Response filed Jul. 11, 2007 to Non-Final Office Action mailed Mar. 13, 2007”, 11 pgs.
“U.S. Appl. No. 10/911,249, Response filed Jul. 29, 2008 to Final Office Action mailed Jan. 29, 2008”, 19 pgs.
“U.S. Appl. No. 10/911,249, Response filed Nov. 30, 2009 to Non Final Office Action mailed Sep. 21, 2009”, 17 pgs.
“U.S. Appl. No. 10/911,249, Response filed Dec. 14, 2007 to Non Final Office Action mailed Sep. 20, 2007”, 9 pgs.
“U.S. Appl. No. 10/911,249, Response to Non-Compliant Amendment filed Nov. 24, 2008”, 25 pgs.
“U.S. Appl. No. 10/911,249, Response to Notice of Non-Compliant Amendment filed Jun. 2, 2005”, 5 pgs.
“U.S. Appl. No. 11/054,717, Final Office Action mailed Mar. 29, 2010”, 5 pgs.
“U.S. Appl. No. 11/054,717, Final Office Action mailed Jun. 1, 2007”, 4 pgs.
“U.S. Appl. No. 11/054,717, Non-Final Office Action mailed Jan. 9, 2009”, 10 pgs.
“U.S. Appl. No. 11/054,717, Non-Final Office Action mailed Jul. 15, 2010”, 4 pgs.
“U.S. Appl. No. 11/054,717, Non-Final Office Action mailed Sep. 11, 2007”, 3 pgs.
“U.S. Appl. No. 11/054,717, Non-Final Office Action mailed Oct. 23, 2006”, 4 pgs.
“U.S. Appl. No. 11/054,717, Notice of Allowance mailed Nov. 3, 2010”, 21 pgs.
“U.S. Appl. No. 11/054,717, Preliminary Amendment filed Feb. 9, 2005”, 3 pgs.
“U.S. Appl. No. 11/054,717, Response filed May 11, 2009 to Non Final Office Action mailed Jan. 9, 2009”, 12 pgs.
“U.S. Appl. No. 11/054,717, Response filed Jun. 1, 2010 to Final Office Action mailed Mar. 29, 2010”, 11 pgs.
“U.S. Appl. No. 11/054,717, Response filed Aug. 1, 2007 to Final Office Action mailed Jun. 1, 2007”, 6 pgs.
“U.S. Appl. No. 11/054,717, Response filed Aug. 10, 2010 to Non Final Office Action mailed Jul. 15, 2010”, 9 pgs.
“U.S. Appl. No. 11/054,717, Response filed Oct. 10, 2007 to Non-Final Office Action mailed Sep. 11, 2007”, 5 pgs.
“U.S. Appl. No. 11/054,717, Response filed Nov. 26, 2008 to Restriction Requirement mailed Nov. 20, 2008”, 9 pgs.
“U.S. Appl. No. 11/054,717, Response filed Dec. 5, 2006 to Non-Final Office Action mailed Oct. 23, 2006”, 9 pgs.
“U.S. Appl. No. 11/054,717, Restriction Requirement mailed Nov. 20, 2009”, 5 pgs.
“U.S. Appl. No. 11/054,717, Supplemental Amendment filed Oct. 24, 2008”, 8 pgs.
“U.S. Appl. No. 11/054,717, Supplemental Amendment filed Sep. 30, 2008”, 10 pgs.
“U.S. Appl. No. 12/034,932, 312 Amendment filed Jul. 1, 2010”, 2 pgs.
“U.S. Appl. No. 12/034,932, Examiner Interview Summary mailed Jan. 15, 2010”, 4 pgs.
“U.S. Appl. No. 12/034,932, Final Office Action mailed May 7, 2010”, 4 pgs.
“U.S. Appl. No. 12/034,932, Non-Final Office Action mailed Sep. 10, 2009”, 5 pgs.
“U.S. Appl. No. 12/034,932, Notice of Allowance mailed Jun. 9, 2010”, 4 pgs.
“U.S. Appl. No. 12/034,932, Preliminary Amendment filed Aug. 18, 2008”, 14 pgs.
“U.S. Appl. No. 12/034,932, PTO Response to 312 Amendment mailed Jul. 8, 2010”, 2 pgs.
“U.S. Appl. No. 12/034,932, Response filed Feb. 10, 2010 to Non Final Office Action mailed Sep. 10, 2009”, 16 pgs.
“U.S. Appl. No. 12/034,932, Response filed May 14, 2010 to Final Office Action mailed May 7, 2010”, 7 pgs.
“U.S. Appl. No. 12/193,562, Examiner Interview Summary mailed Jan. 13, 2010”, 4 pgs.
“U.S. Appl. No. 12/193,562, Final Office Action mailed Mar. 24, 2010”, 5 pgs.
“U.S. Appl. No. 12/193,562, Non-Final Office Action mailed Sep. 9, 2009”, 5 pgs.
“U.S. Appl. No. 12/193,562, Notice of Allowance mailed Jun. 15, 2010”, 8 pgs.
“U.S. Appl. No. 12/193,562, Response filed May 24, 2010 to Final Office Action mailed Mar. 24, 2010”, 8 pgs.
“U.S. Appl. No. 12/193,562, Response filed Dec. 9, 2009 to Non-Final Office Action mailed Sep. 9, 2009”, 17 pgs.
“U.S. Appl. No. 12/193,562, Supplemental Response filed Feb. 9, 2010 to Non Final Office Action mailed Sep. 9, 2009”, 9 pgs.
“U.S. Appl. No. 12/193,573, Examiner Interview Summary filed May 19, 2010”, 1 pg.
“U.S. Appl. No. 12/193,573, Examiner Interview Summary mailed Jan. 13, 2010”, 4 pgs.
“U.S. Appl. No. 12/193,573, Non-Final Office Action mailed Apr. 7, 2009”, 11 pgs.
“U.S. Appl. No. 12/193,573, Non-Final Office Action mailed Sep. 11, 2009”, 5 pgs.
“U.S. Appl. No. 12/193,573, Notice of Allowance mailed May 5, 2010”, 9 pgs.
“U.S. Appl. No. 12/193,573, Response filed Feb. 10, 2010 to Non Final Office Action mailed Sep. 11, 2009”, 18 pgs.
“U.S. Appl. No. 12/193,573, Response filed Jun. 15, 2009 to Non Final Office Action mailed Apr. 7, 2009”, 19 pgs.
“U.S. Appl. No. 12/193,578, 312 Amendment filed May 19, 2010”, 2 pgs.
“U.S. Appl. No. 12/193,578, Non-Final Office Action mailed Feb. 11, 2009”, 12 pgs.
“U.S. Appl. No. 12/193,578, Non-Final Office Action mailed Sep. 11, 2009”, 5 pgs.
“U.S. Appl. No. 12/193,578, Notice of Allowance mailed Apr. 22, 2010”, 7 pgs.
“U.S. Appl. No. 12/193,578, PTO Response to 312 Amendment mailed Jun. 4, 2010”, 2 pgs.
“U.S. Appl. No. 12/193,578, Response filed Feb. 10, 2010 to Non Final Office Action mailed Sep. 11, 2009”, 20 pgs.
“U.S. Appl. No. 12/193,578, Response filed Jun. 15, 2009 to Non-Final Office Action mailed Feb. 11, 2009”, 16 pgs.
“U.S. Appl. No. 12/218,260, Examiner Interview Summary mailed Jun. 10, 2010”, 3 pgs.
“U.S. Appl. No. 12/218,260, Examiner Interview Summary filed May 24, 2010”, 1 pg.
“U.S. Appl. No. 12/218,260, Examiner Interview Summary mailed Apr. 23, 2010”, 3 pgs.
“U.S. Appl. No. 12/218,260, Non Final Office Action mailed Nov. 3, 2009”, 3 pgs.
“U.S. Appl. No. 12/218,260, Non-Final Office Action mailed Jan. 2, 2009”, 11 pgs.
“U.S. Appl. No. 12/218,260, Notice of Allowance mailed Apr. 1, 2010”, 9 pgs.
“U.S. Appl. No. 12/218,260, Preliminary Amendment filed Jul. 11, 2008”, 9 pgs.
“U.S. Appl. No. 12/218,260, Preliminary Amendment filed Sep. 10, 2009”, 10 pgs.
“U.S. Appl. No. 12/218,260, Response filed Apr. 2, 2009 to Non Final Office Action mailed Jan. 2, 2009”, 7 pgs.
“U.S. Appl. No. 12/218,260, Response filed Dec. 3, 2009 to Non Final Office Action mailed Nov. 3, 2009”, 12 pgs.
“U.S. Appl. No. 12/218,260, Supplemental Notice of Allowability mailed Jun. 10, 2010”, 6 pgs.
“U.S. Appl. No. 12/875,445 , Response filed Nov. 1, 2011 to Non Final Office Action mailed Sep. 26, 2011”, 12 pgs.
“U.S. Appl. No. 12/875,445, Non Final Office Action mailed Sep. 26, 2011”, 6 pgs.
“U.S. Appl. No. 12/875,445, Non-Final Office Action mailed Dec. 2, 2011”, 5 pgs.
“U.S. Appl. No. 12/955,512, Non Final Office Action mailed Nov. 10, 2011”, 7 pgs.
“U.S. Appl. No. 12/955,512, Notice of Allowance mailed Feb. 21, 2012”, 6 pgs.
“U.S. Appl. No. 12/955,512, Response filed Jan. 26, 2012 to Non Final Office Action mailed Nov. 10, 2011”, 13 pgs.
“International Application Serial No. PCT/US00/24633, International Search Report mailed Nov. 30, 2000”, 7 pgs.
“International Application Serial No. PCT/US99/20823, International Preliminary Examination Report mailed Sep. 19, 2000”, 14 pgs.
“International Application Serial No. PCT/US99/20823, International Search Report mailed Dec. 13, 1999”, 8 pgs.
“International Application Serial No. PCT/US99/20823, International Written Opinion mailed May 16, 2000”, 15 pgs.
“U.S. Appl. No. 12/875,445 , Response filed Aug. 13, 2012 to Final Office Action mailed Jun. 13, 2012”, 10 pgs.
“U.S. Appl. No. 12/875,445 , Response filed Aug. 29, 2012 to Non Final Office Action mailed Aug. 24, 2012”, 9 pgs.
“U.S. Appl. No. 12/875,445, Non Final Office Action mailed Aug. 24, 2012”, 6 pgs.
“U.S. Appl. No. 12/875,445, Notice of Allowance mailed Sep. 19, 2012”, 6 pgs.
Related Publications (1)
Number Date Country
20120202020 A1 Aug 2012 US
Continuations (2)
Number Date Country
Parent 12955512 Nov 2010 US
Child 13447886 US
Parent 11054717 Feb 2005 US
Child 12955512 US