Radiation imagery chemistry: process – composition – or product th – Imaged product – Antifraud or antitampering
Reexamination Certificate
1999-09-09
2001-04-24
Goodrow, John (Department: 1753)
Radiation imagery chemistry: process, composition, or product th
Imaged product
Antifraud or antitampering
C283S081000, C283S094000
Reexamination Certificate
active
06221545
ABSTRACT:
BACKGROUND OF THE INVENTION
This invention relates to adhesives for use in multilayer laminates in which at least one of the layers includes an ink-bearing surface.
There has been an interest in printing images such as photographic images onto plastic substrates. It would be particularly desirable to use liquid toner-based electrophotographic printing for this purpose because this printing technique produces high quality images.
Once the image has been printed onto the surface of the plastic substrate, it is necessary to apply a protective film over the printed ink-bearing surface. The bond strength between the protective film and the printed surface must be sufficient to resist delamination under typical use conditions.
SUMMARY OF THE INVENTION
In one aspect, the invention features an adhesive composition that includes the reaction product of: (a) a polyester-based polyurethane; (b) an epoxy resin; (c) an epoxy-functional silane; and (d) an isocyanate-functional compound. The adhesive compositions are useful for preparing multilayer laminates in which a major surface of a first polymeric substrate is bonded to a major surface of a second polymeric substrate through the adhesive composition. One or both of those major surfaces includes an ink-bearing image.
The adhesive compositions exhibit good adhesion (as measured by the 180 degree peel strength) to both ink-bearing polymeric substrates and non-ink bearing polymeric substrates. The compositions are particularly useful where the ink is an electrophotographic ink. Examples of suitable electrophotographic inks include polymers having a Tg no greater than about 30° C., while in other embodiments the ink includes a polymer having a Tg greater than about 30° C.
One example of a suitable ink is derived from gel organosol-containing, liquid toner compositions described, e.g., in Baker et al., U.S. Pat. No. 5,652,282 and Baker et al., U.S. Pat. No. 5,698,616, each of which is hereby incorporated by reference. These toners include (a) a carrier liquid (e.g., an aliphatic hydrocarbon carrier liquid having a Kauri-Butanol number less than 30) and (b) a (co)polymeric steric stabilizer having a molecular weight greater than or equal to 50,000 Daltons and a polydispersity less than 15 covalently bonded to a thermoplastic (co)polymeric core that is insoluble in the carrier liquid. The core preferably has a Tg no greater than about 30° C. The toner may further include a colorant and a charge director. Also suitable are non-gel organosol-containing liquid toner compositions described, for example, in Baker et al., U.S. Pat. No. 5,886,067, hereby incorporated by reference.
Another example of a suitable ink is derived from liquid toners described in Landa et al., U.S. Pat. No. 4,794,651; Landa et al., U.S. Pat. No. 4,842,974; Landa et al., U.S. Pat. No. 5,047,306; Landa et al., U.S. Pat. No. 5,047,307; Landa et al., U.S. Pat. No. 5,192,638; Landa et al., U.S. Pat. No. 5,208,130; Landa et al., U.S. Pat. No. 5,225,306; Landa et al., U.S. Pat. No. 5,264,313; Landa et al., U.S. Pat. No. 5,266,435; Landa et al., U.S. Pat. No. 5,286,593; Landa et al., U.S. Pat. No. 5,346,796; Landa et al., U.S. Pat. No. 5,407,771 and Landa, WO92/17823 published Oct. 15, 1992 entitled “Polymer Blends,” each of which is hereby incorporated by reference.
The compositions are also useful with inks such as ink jet inks and lithographic inks. Any of these inks may be used alone or in combination with each other. For example, the ink-bearing surface may include electrophotographically printed areas featuring an electrophotographic ink and offset printed areas featuring a lithographic ink. Preferably, however, all the printed areas of the laminate are electrophotographically printed areas featuring an electrophotographic ink.
The adhesive compositions exhibit good adhesion to a number of polymeric substrates. In one preferred embodiment, the adhesive is used to bond a rigid core layer to a flexible overlay film, where at least one of these materials includes an ink-bearing surface. Preferably, at least one of the substrates is substantially transparent to permit viewing of the printed image on the ink-bearing surface.
Examples of suitable polymeric substrates are selected from the group consisting of polyvinyl chloride, vinyl chloride-vinyl acetate copolymers, polyesters, polyolefins, polycarbonates, and combinations thereof. Also suitable are microporous substrates such as Teslin™ films commercially available from PPG, Inc. of Pittsburgh, Pa. One preferred construction includes a polyvinyl chloride substrate adhesively bonded to a substantially transparent polyester overlay film.
The adhesive compositions are also useful for preparing laminated articles having more than two substrates. For example, the article may include a core substrate having a pair of opposed major surfaces, each of which is bonded to a separate overlay film. Such constructions are particularly useful for articles having printed images on two different surfaces.
In a second aspect, the invention features a lamination process for preparing the above-described articles. The ink-bearing image preferably is performed according to an electrophotographic imaging process that includes:
(i) charging the surface of an electrophotographic photoreceptor;
(ii) imagewise exposing the charged surface of the photoreceptor to radiation to dissipate charge in selected areas and thereby form a latent image on the photoreceptor surface;
(iii) contacting the latent image with a toner to form a toned image; and
(iv) transferring the toned image to the major surface of the first polymeric substrate.
The toner preferably is a liquid toner. Preferred liquid toners, in turn, include a film-forming polymer. In some embodiments, the film-forming polymer has a Tg no greater than about 30° C., while in other embodiments the film-forming polymer has a Tg greater than about 30° C. Following lamination, the article may subjected to a number of operations, including slitting, cutting, hole punching and drilling, foil stamping, sewing and grommeting, foil stamping, perforation, folding, surface texturing, and the like.
Other features and advantages of the invention will be apparent from the following description of the preferred embodiments thereof, and from the claims.
DETAILED DESCRIPTION
The invention will now be described further by way of the following examples.
The black, positive-acting, film-forming, electrophotographic ink used in the examples was prepared at an organosol/pigment ratio of 6 following the procedure described in Example 40 of U.S. Pat. No. 5,652,282 modified as follows.
The gel organosol prepared according to the procedure of Example 22 of U.S. Pat. No. 5,652,282 was mixed using a Silverson mixer (Model L2R, Silverson Machines, Ltd.) operated at the lowest speed setting. After mixing for five minutes, 1912 g of the homogenized organosol at 16.14% (w/w) solids in NORPAR 12 were combined with 1031 g of NORPAR 12 (Exxon Chemical Co., Houston, Tex.), 51 g of MONARCH 120 carbon black (Cabot Corp., Billerica, Mass.), and 6.08 g of Zirconium HEX-CEM (OMG Chemical Company, Cleveland, Ohio) in a 4.0 liter polyethylene container. This mixture was then milled in ten vertical bead mills, each having a capacity of 0.5 liter (Model 6TSG-1/4, Aimex Co. Ltd., Tokyo, Japan) by placing 300 g of millbase and 390 g of 1.3 mm diameter Potters glass beads (Potters Industries, Inc., Parsippany, N.J.) in each mill. Each mill was operated at 2,000 rpm for 1.5 hours without cooling water circulating through the cooling jacket of the milling chamber.
A portion of the 12% (w/w) solids toner concentrate thus formed was diluted to approximately 3% (w/w). This dilute toner sample exhibited the following properties, as determined using the test methods described in U.S. Pat. No. 5,652,282:
Number Mean Particle Size: 0.261 micron
Bulk Conductivity: 149 picoMhos/cm
Percent Free Phase Conductivity: 5%
Dynamic Mobility: 0.0402 micron-cm/[volt-second]
This 3% toner was tested on the toner plating apparatus described in U.S. Pat. No. 5,65
Baker James A.
Herman Gay L.
Jalbert Claire A.
Li Minyu
Morrison Eric D.
Goodrow John
Imation Corp.
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