This application relates generally to designs and transfers and specifically to a flocked stretchable design or transfer.
It is often desirable to decorate clothing or other articles with designs that have various surfaces, such as designs that have a flocked surface such that the surface is fuzzy. Using flocked designs works well with clothes or other articles that are not meant to be stretched. To date, flocked designs have not been used with stretchable articles since the flock adhesive layer and, thus, the design, tends to permanently splits or cracks, sometimes without recovery, as the material is stretched. This is undesirable since the design becomes severely deformed. It is also undesirable since the flock fibers may become detached from the transfer or design, leaving permanent holes, voids, or gaps in the design. Another undesirable aspect of using flocked designs on stretchable articles is that the stretchable article may not reform to its original size and shape near the flocked design due to the adhesive used to keep the flocked design on the clothing or article.
Today's fashions are often characterized by stretchable materials, whether the stretchable material is a knitted material, nylon, polyester, elastic or other material. Thus, a wide market of clothing does not use flocked designs because of the undesirable characteristics associated therewith. What is needed is a flocked stretchable design or transfer that can be stretched with the clothing or other article that will reform to its original design without loss of design quality or adhesion or integrity of the image.
The present invention describes a flocked stretchable design and a process for producing a flocked stretchable design, appliqué, or transfer. The design can have shape memory even when stretched to a high degree.
In one embodiment, the design is configured as a transfer. The transfer includes a sacrificial carrier layer or release sheet, a release adhesive or binder applied to the carrier layer, a plurality of (preferably multi-colored) flock fibers releasably or temporarily attached to the release adhesive, an elastic (e.g., elastomeric) film, and a first (preferably continuously distributed) activatable adhesive layer (e.g., a thermoset or hot melt thermoplastic adhesive) permanently bonded to a first side of the elastic film. The plurality of flock fibers is permanently bonded to the first side of elastic film using the first activatable adhesive layer. A second activatable, continuously or discontinuously distributed, (elastomeric) adhesive layer is bonded to an opposing, second side of the elastic film.
While not wishing to be bound by any theory, it is believed that, when the second activatable adhesive layer is discontinuously distributed, the gaps or spaces (or discontinuities) in the second activatable adhesive layer may assist the shape memory of the design. The discontinuities in the second activatable adhesive layer may not only provide expansion room for the adhesive when deformed but also prevent the adhesive from flowing into the deformation voids in the adjacent, stretched flock layer by reducing the total mass while still providing effective point-by-point adhesion. The discontinuities are preferably retained after the design is bonded to a suitable substrate. When the second discontinuous activatable adhesive is activated to bond the design to a desirable substrate, it is believed that the second discontinuous activatable adhesive layer soaks, flows, or “wicks” down into the substrate, vertically not laterally, on which the design or transfer is mounted maintaining the voids. This wicking can allow the substrate and the design to stretch at the same rate and reform to their respective original shapes without permanent deformation of either the substrate and the design or the interface between them.
In another embodiment, the design is direct flocked and includes the elastic film, the first (preferably wet coated) activatable adhesive layer, a plurality of flock fibers, and the second activatable adhesive layer. As will be appreciated, the design of this embodiment does not include a transfer carrier layer and a release adhesive.
In other embodiments, the present invention also includes methods of producing both the design of both configurations.
The various embodiments of the present invention can have a number of advantages compared to conventional designs. For example, the stretchable transfer or design of the present invention can prevent the flock fiber adhesive layer from becoming detached from the design or transfer, before, during and after the transfer or design is stretched. The design can have shape memory and can reform, after being stretched, substantially to its original shape and size without loss of original design integrity and aesthetic appeal. The design can, when stretched to a high degree, evidence an increase in the inter flock distance (i.e., the horizontal space between individual fibers) without the flock becoming disengaged from the substrate. The design can combine the multicolored plush design that is attainable with flocked fibers with high elasticity and shape memory. The flock fibers are stable and do not become detached from the design, before, during and after the transfer or design is stretched. The aesthetic quality of the design can be retained after any number of elastic deformations. The design can be applied to a variety of elastic substrates that have previously been unsuitable for flocked designs. Examples include highly elastic substrates such as Lycra®, and elastomeric materials, such as rubber and latex, elastic woven or knit waist band such as for men's underwear or women's panties, etc.
These and other objects, features, and advantages of the invention will become apparent from the following best mode description, the drawings and the claims.
As shown in
The elastic film should be durable, thermally stable, and able to resist the various treatments including but not limited to flocking and/or lamination process, applying chemicals, washing, heating, drying, both during the flocking process and after the design or transfer has been heat applied to the article. The term “elastic” as used herein means those materials that have the ability to regain, at least substantially, their original shape after a load is removed. The elastic film preferably has a modulus of elasticity of less than about 11.25 pounds per foot (“lbf”) (50 N). The modulus of elasticity for the material selected is preferably above about 0.5 lbf (2.22 N) (where the modulus is defined as the force required to pull a ¼ inch sample from 3 inches to 6 inches). As the modulus of elasticity (Young's Modulus) is a fundamental material constant, the modulus is an index of the stiffness of the material. A higher value of the modulus indicates a more brittle material (i.e. glass, ceramics). A very low value represents a elastomeric material (i.e. rubber). The elastic film preferably has an elongation of at least about 200% and more preferably at least about 300% and a recovery of at least about 75% and more preferably at least about 95%. The recovery is the percent of the film's shape retained after the film is stretched to 100% of its original length at a rate of 30 inches per minute and the stretched film allowed to retract freely for 1 minute.
The elastic material can be of any suitable composition, such as rubber, polyurethane, and elastomers. Particularly preferred elastic materials include natural vulcanized rubber and elastomers, such as styrene-butadiene copolymer, polychloroprene (neoprene), nitrile rubber, butyl rubber, polysulfide rubber (Thiokol), cis-1,4-polyisoprene, ethylene-propylene terpolymers (EPDM rubber), silicone rubber, (thermoplastic) polyurethane such as Spandex, and polyurethane rubber. As will be appreciated, “elastomers” refer to synthetic thermosetting (typically high) polymers having properties similar to those of vulcanized natural rubber, namely the ability to be stretched to at least twice their original length and to retract quickly to approximately their original length when released. It has been found that materials with the trade name Clarense® from Bemis, Lycra® from Du Pont, and Dorlastan® from Bayer work well with the present invention.
The elastic film preferably has a thickness ranging from about 1 mil to 25 mils and more preferably, from about 1 mil to 15 mils.
The first activatable adhesive layer 13 is applied to the elastic film 12. The first activatable adhesive layer is preferably distributed continuously over the first surface 18 of the elastic film. The first activatable adhesive preferably has a thickness ranging from about 1 mil to 10 mils and more preferably from about 1 mil to about 3 mils. The first activatable adhesive layer provides a permanent grip of the flock fibers. The first activatable adhesive layer can be applied to the elastic film in any number of ways, e.g., applied as a liquid using suitable techniques or as a pre-formed film and either can be applied to the flock fibers simultaneously. Suitable adhesives for the first activatable adhesive are described in detail below.
The plurality of flock fibers 14 are flocked onto the first activatable adhesive layer through general and conventional flocking methods and techniques. The flock can be of multiple colors, which can be arranged in a pre-selected design, or can be of a single color. The flock 14 used in any of the processes discussed herein can be any electrostatically chargeable fiber, such as fibers made from rayon, nylon, cotton, acrylic, and polyester. Preferably, the flock has a melting and/or softening point that is greater than the temperatures experienced by the flock during activation of the first and second adhesives. Due to its low melt point, acrylic flock is undesirable in many applications. The flock is also preferably resilient under the temperatures and pressures experienced in design manufacturing and later application processes to resist softening, deformation, and melting. Resilient flock, such as rayon, nylon, and terepthalate (e.g., poly(cyclohexylene-dimethylene terephthalate) polymer flock, is particularly preferred. In most applications, the flock orientation is at least substantially orthogonal (perpendicular) to the first side of the elastic film.
In accordance with the present invention, to achieve a multicolor and/or textured effect, the flock 14 is applied through the image screen which is preferably a gauze-like mesh screen made of polyester monofilament material or by inkjet printing or sublimation transfer before the first and second activatable adhesive layers and elastic film are applied to the flock. The multicolor effect is achieved by using different precolored flock. A textured effect is achieved by using flock fibers of different length and passing flock fibers of substantially the same or uniform length in batches through the open section of the barrier. As used herein, precolored flock means that the flock has been colored before being flocked, adhered stuck or otherwise applied to the release adhesive. Depending on the overall design texture and the color or number of colors of flock which are to be used, an appropriate number of barriers or screens are prepared to have open sections to permit passage of flock in a predetermined configuration, texture pattern, and/or color pattern. Alternatively, a single screen may be sequentially masked for this purpose. In either case, the open sections of each mask or screen are designed to permit passage of flock fibers in a configuration which corresponds to areas of the final design including any surrounding bleed areas which correspond to only one color and/or flock length, which is preferably one of a plurality of colors and/or fiber lengths of a color and/or texture pattern, intended to be used in the final or overall design. The screen also serves to mask areas which are not intended to receive a particular color or texture. In accordance with the present invention, each different color and/or different length of flock is preferably applied sequentially using a different screen to result in the particular precolored flock and/or flock of predetermined length passing through the open section of the screen onto a corresponding section of the release adhesive 21 to form a color and/or texture pattern.
The present invention generally utilizes the general materials and flocking techniques found in U.S. Pat. Nos. 3,793,050; 4,292,100; and 4,396,662 and UK patent application Nos. 2,065,031 and 2,126,951 all of which are incorporated by reference herein. The present invention can also utilize flocking materials and techniques such as those described in U.S. Pat. Nos. 4,810,549; 5,047,103; 5,207,851; 5,346,746; 5,597,637; 5,858,156; 6,010,764; 6,083,332; and 6,110,560 as well as copending patent applications U.S. application Ser. Nos. 29/058,551 filed Aug. 19, 1996; 09/548,839 filed Apr. 13, 2000; 09/621,830 filed Jul. 24, 2000; 09/735,721 filed Dec. 13, 2000; 09/629,746 filed Jul. 31, 2000; 09/973,113 filed Oct. 9, 2001; 60/327,642 filed Oct. 5, 2001; 60/344,863 filed Nov. 8, 2001; 60/366,580 filed Mar. 21, 2002; 60/332/,647 filed Nov. 21, 2001 and 60/393,362 filed Jul. 3, 2002, 10/265,206 filed Oct. 4, 2002, and 10/394,357, filed Mar. 21, 2003, of which I am an inventor. These patents and patent applications are also incorporated herein as if set forth in their entireties.
Returning again to
The term “discontinuous” means that the adhesive, when applied to the elastic film, does not coat the entirety of the film but allows for holes or voids, shown in
To prevent elimination of the voids when the discontinuous adhesive film is thermally adhered to the elastic film and/or substrate, it is preferred that the viscosity of the adhesive film be high enough such that there is no lateral flow together to melt and flow into the voids between the adhesive segments. The thickness of the second activatable, discontinuously distributed, adhesive layer preferably ranges from about 1 mil to 25 mils and more preferably from about 2 mils to 10 mils and even more preferably from about 2 mils to 5 mils.
Any suitable adhesive can be used for the first and second activatable adhesives. The first and second activatable adhesives typically have differing compositions. As will be appreciated, suitable adhesives fall into two general categories, namely organic and inorganic adhesives, with organic adhesives being preferred. Although either natural organic or synthetic adhesives are suitable, synthetic adhesives are preferred. Synthetic adhesives include elastomer-solvent cements, thermoplastic resins (for hot-melts) (e.g., polyethylene, isobutylene, polyamides, and polyvinyl acetate), thermosetting resins (e.g., epoxy, phenoformaldehyde, polyvinyl butryal, and cyanoacrylates), polyesters, polynrethanes, and silicone polymers and cements. Of the synthetic adhesives, thermoplastic (hot melt) resins and thermosetting resins are preferred. Thermoset adhesives solidify or set irreversibly when heated above a certain temperature. This property is usually associated with a cross-linking reaction of the molecular constituents induced by heat or radiation.
Suitable thermoset adhesives can include curing agents or catalysts such as organic peroxides, sulfur, isocyanate, oxalic acids, or diammonium phosphate. Thermosetting resins such as methylol-melamines, urea formaldehyde condensates or phenol formaldehyde condensates may be incorporated to improve durability or abrasion resistance of the design. Suitable examples of thermosetting adhesives include polyethylene, phenolics, alkyds, amino resins, polyesters, epoxides, and silicones. For use with the present invention a polyester, a polyurethane, or a polyamide second activatable, discontinuously distributed, adhesive layer is preferred.
The adhesive can have any form, namely be in the form of a liquid, solid (such as a pre-formed film), or a gas (which is condensed onto the desired surface). As will be appreciated, liquid adhesives include without limitation, water-based, solvent based, or curable liquid systems. Water-based adhesives generally consist of a binder, usually an emulsion polymer, and a viscosity builder. Water-based adhesives may also contain plasticizers, thermosetting resins, curing catalysts, stabilizers and various other additives known in the art. The emulsion polymer is generally chosen from acrylic, vinyl-acrylic, vinyl, urethane, and styrene-butadiene latexes. The viscosity is dictated by the substrate and the specific adhesive. Suitable viscosity builders are typically water soluble polymers such as such as carboxymethyl cellulose, hydroxyethyl cellulose, polyoxyethylenes and natural gums as well as alkyl swellable polymers, such as, highly carboxylated acrylic emulsion polymers.
Plasticizers may be added to alter the properties of the design or to improve the flow and levelling characteristics of the adhesive. Where the primary goal is the latter, fugitive plasticizers, such as, the phthalate esters may be employed. If the intent is to alter the properties of the finished goods, then more permanent plasticizers such as low molecular weight polyesters may be used.
Solvent adhesives include those fully reacted soluble polymers, such as, acrylic homo and copolymers, polyesters, polyamides or polyurethanes and two package systems, such as, polyester polyols with diisocyanates, or isocyanate prepolymers and epoxies with polyamines. The polymer or prepolymer is dissolved in a suitable solvent which is preferably low boiling, and then thickened to the proper viscosity in a manner similar to that used for the water-base adhesives. Catalysts, cross-linking agents, stabilizers, pigments, or dyes may also be incorporated.
Curable liquid systems include 2 part urethanes, e.g., a dlisocyanate and a polymeric polyol, flexible epoxy systems, e.g., liquid epoxy resins or solutions of solid epoxy resins co-reacted with polyamides or polyamines and dimercaptans and a polyene with a peroxide. Also, hot melts can be used, such as polyethylene-vinylacetate copolymer, polyethylene-ehylacrylate copolymer, and a plasticized polyvinyl chloride in the form of a plastisol which can be heated to fuse and then cure. In one design configuration, the first activatable adhesive is preferably a thermoset adhesive while the second activatable adhesive is preferably a hot melt thermoplastic adhesive. The preferred adhesive for the first activatable adhesive is a thermosetting or thennoplastic hot melt film. To provide the desired discontinuities 15, preferred, pre-formed adhesive films for the second activatable adhesive include (spun) web adhesives such as the Sharnet® adhesive from Bostik-Findley.
The release adhesive 21 is applied to the carrier film to bind the flock fibers in a certain orientation before the flock fibers are collectively bonded by the first activatable adhesive layer. The release adhesive is a composition which when subjected to the usual curing conditions, e.g., heat, ultra-violet, etc., will not permanently set or permanently adhere to the substrate or to the flock. Such compositions typically include but are not limited to waxes, low molecular weight polyethylenes, polystyrenes, hot melt slurries (such as polyesters, polyamides, polyethylenes, and urethane hot melt), and the like. Additionally, starched-based adhesives such as, canary dextron and British Gum; gums, such as gum arabic and gum tragacanth; water soluble, non-curing polymers, such polyvinyl alcohols, particularly hydrolyzed polyvinyl acetate and the like may be used. Another example of appropriate composition is glycerine and urea.
To produce a transfer according to the present invention and with reference to
To produce the design 10 through a direct flock method according to the present invention and with reference to
In one continuous process configuration shown in
The hot melt adhesive 16 is then applied to the binder 17 as a separate layer. In addition, other heat sensitive adhesives, such as polyvinyl chloride, thermoplastic acrylic resin, polyethylene, polyamide, polyurethane, paraffin and rubber derivative may be used for this purpose, with polyurethane being preferred.
In an alternative embodiment, the second activatable layer is continuously distributed as opposed to being discontinuously distributed. To prevent loss of shape memory or design appearance, the adhesive layer is selected to have the proper stretch and recovery characteristics. Examples of suitable adhesives include polyurethanes, polyesters, polyamides, polyolefins, and other elastomeric adhesives.
In one alternative embodiment, the elastic film 12 of the present invention can be used as the film backing of a co-molded direct flock and flock transfer such as that described in U.S. patent application Ser. No. 60/393362, filed Jul. 3, 2002, or in place of the barrier layer 204 described in
In another alternative embodiment, the elastic film 12 and second activatable adhesive layer 11 of the present invention can also be used as an optional layer in the screen printed resin film design or transfer made from a liquid plastic dispersion such as that described in U.S. patent application Ser. Nos. 60/332,647, filed Nov. 21, 2001; 60/344,862 filed Nov. 8, 2001; and 60/327,642, filed Oct. 5, 2001. The entireties of these patent applications are incorporated herein as fully set forth.
In yet another alternative embodiment, the design is configured as a sew-on patch. When so configured, the second activatable adhesive layer can be eliminated or can be used sparingly to provide additional bonding capabilities, such as alignment before stitching. The elastomeric film provides integrity and can be sewn on.
As one can observe from
The principles, preferred embodiments and modes of operation of the present invention have been described in the foregoing specification. The invention which is intended to be protected herein should not, however, be construed as limited to the particular forms disclosed, as these are to be regarded as illustrative rather than restrictive. Variations and changes may be made by those skilled in the art without departing from the spirit of the present invention. Accordingly, the foregoing best mode of carrying out the invention should be considered exemplary in nature and not as limiting to the scope and spirit of the invention as set forth in the appended claims.
The present application claims the benefits of U.S. Provisional Patent Application Ser. Nos. 60/403,992, filed Aug. 16 2002; and 60/405,473, filed Aug. 23, 2002, all to Abrams, each of which is incorporated herein by this reference.
Number | Name | Date | Kind |
---|---|---|---|
1905999 | Ellis | Apr 1933 | A |
2592602 | Saks | Apr 1952 | A |
2636837 | Summers | Apr 1953 | A |
2999763 | Sommer | Sep 1961 | A |
3215584 | McConnell et al. | Nov 1965 | A |
3314845 | Perri | Apr 1967 | A |
3377232 | Mencock et al. | Apr 1968 | A |
3459579 | Newman | Aug 1969 | A |
3496054 | Baigas | Feb 1970 | A |
3529986 | Kappas et al. | Sep 1970 | A |
3565742 | Stephens et al. | Feb 1971 | A |
3622434 | Newman | Nov 1971 | A |
3644267 | Jackson, Jr. et al. | Feb 1972 | A |
3657060 | Haigh | Apr 1972 | A |
3660200 | Anderson et al. | May 1972 | A |
3674611 | Petry et al. | Jul 1972 | A |
3772132 | Dulin, Jr. | Nov 1973 | A |
3775205 | Hermann et al. | Nov 1973 | A |
3793050 | Mumpower, Jr. | Feb 1974 | A |
3803453 | Hull | Apr 1974 | A |
3816211 | Haigh | Jun 1974 | A |
3837946 | Gribbin | Sep 1974 | A |
3887737 | Baxter et al. | Jun 1975 | A |
3900676 | Alderson | Aug 1975 | A |
3903331 | Klein | Sep 1975 | A |
3917883 | Jepson | Nov 1975 | A |
3936554 | Squier | Feb 1976 | A |
3956552 | Geary | May 1976 | A |
3961116 | Klein | Jun 1976 | A |
3969559 | Boe | Jul 1976 | A |
3979538 | Gilman et al. | Sep 1976 | A |
3989869 | Neumaier et al. | Nov 1976 | A |
4018956 | Casey | Apr 1977 | A |
4025678 | Frank | May 1977 | A |
4031281 | Keeling | Jun 1977 | A |
4034134 | Gregorian et al. | Jul 1977 | A |
4035532 | Gregorian et al. | Jul 1977 | A |
4062992 | Power et al. | Dec 1977 | A |
4088708 | Riew | May 1978 | A |
4120713 | Jensen et al. | Oct 1978 | A |
4142929 | Otomine et al. | Mar 1979 | A |
4201810 | Higashiguchi | May 1980 | A |
4218501 | Kameya et al. | Aug 1980 | A |
4269885 | Mahn | May 1981 | A |
4273817 | Matsuo et al. | Jun 1981 | A |
4282278 | Higashiguchi | Aug 1981 | A |
4292100 | Higashiguchi | Sep 1981 | A |
4314813 | Masaki | Feb 1982 | A |
4340632 | Wells et al. | Jul 1982 | A |
4362773 | Shikinami | Dec 1982 | A |
4362924 | Story et al. | Dec 1982 | A |
4385588 | Bennetot | May 1983 | A |
4387214 | Passmore et al. | Jun 1983 | A |
4390387 | Mahn | Jun 1983 | A |
4396662 | Higashiguchi | Aug 1983 | A |
4405401 | Stahl | Sep 1983 | A |
4423106 | Mahn | Dec 1983 | A |
4430372 | Knoke et al. | Feb 1984 | A |
4438533 | Hefele | Mar 1984 | A |
4465723 | Knoke et al. | Aug 1984 | A |
4574018 | Masuda et al. | Mar 1986 | A |
4588629 | Taylor | May 1986 | A |
4652478 | Maii | Mar 1987 | A |
4668323 | Lenards et al. | May 1987 | A |
4681791 | Shibahashi et al. | Jul 1987 | A |
4687527 | Higashiguchi | Aug 1987 | A |
4741791 | Howard et al. | May 1988 | A |
4810549 | Abrams et al. | Mar 1989 | A |
4895748 | Squires | Jan 1990 | A |
4931125 | Volkmann et al. | Jun 1990 | A |
4966801 | Becker et al. | Oct 1990 | A |
4980216 | Römpp | Dec 1990 | A |
5008130 | Lenards | Apr 1991 | A |
5026591 | Henn et al. | Jun 1991 | A |
5041104 | Seal | Aug 1991 | A |
5043375 | Henning et al. | Aug 1991 | A |
5047103 | Abrams et al. | Sep 1991 | A |
5059452 | Squires | Oct 1991 | A |
5077116 | Lefkowitz | Dec 1991 | A |
5198277 | Hamilton et al. | Mar 1993 | A |
5207851 | Abrams | May 1993 | A |
5248536 | Du Katz | Sep 1993 | A |
5346746 | Abrams | Sep 1994 | A |
5350474 | Yamane | Sep 1994 | A |
5352507 | Bresson et al. | Oct 1994 | A |
5383996 | Dressler | Jan 1995 | A |
5447462 | Smith et al. | Sep 1995 | A |
5489359 | Yamane | Feb 1996 | A |
5529650 | Bowers et al. | Jun 1996 | A |
5534099 | Yamamoto | Jul 1996 | A |
5597637 | Abrams et al. | Jan 1997 | A |
5622587 | Barthelman | Apr 1997 | A |
5693400 | Hamilton et al. | Dec 1997 | A |
5762379 | Salmon et al. | Jun 1998 | A |
5766397 | Jones | Jun 1998 | A |
5771796 | Morrison et al. | Jun 1998 | A |
5804007 | Asano | Sep 1998 | A |
5858156 | Abrams et al. | Jan 1999 | A |
5900096 | Zemel | May 1999 | A |
5912065 | Kukoff | Jun 1999 | A |
5981009 | Iacono et al. | Nov 1999 | A |
6010764 | Abrams | Jan 2000 | A |
6083332 | Abrams | Jul 2000 | A |
6110560 | Abrams | Aug 2000 | A |
6113149 | Dukatz | Sep 2000 | A |
6114023 | Schwarz et al. | Sep 2000 | A |
6146485 | Iacono et al. | Nov 2000 | A |
6152038 | Wagner et al. | Nov 2000 | A |
6170881 | Salmon et al. | Jan 2001 | B1 |
6171678 | Holeschovsky et al. | Jan 2001 | B1 |
6202549 | Mitsam et al. | Mar 2001 | B1 |
6224707 | Lion | May 2001 | B1 |
6247215 | Van Alboom et al. | Jun 2001 | B1 |
6249297 | Lion | Jun 2001 | B1 |
6264775 | Holeschovsky et al. | Jul 2001 | B1 |
6296908 | Reihs et al. | Oct 2001 | B1 |
6299715 | Langsdorf et al. | Oct 2001 | B1 |
6350504 | Alboom et al. | Feb 2002 | B1 |
6376041 | Morrison et al. | Apr 2002 | B1 |
6387472 | Reck et al. | May 2002 | B1 |
6428877 | Suss et al. | Aug 2002 | B1 |
6436506 | Pinter et al. | Aug 2002 | B1 |
6451148 | Jenner | Sep 2002 | B1 |
6481015 | Lanier | Nov 2002 | B1 |
6676796 | Pinter et al. | Jan 2004 | B2 |
6787589 | Weaver et al. | Sep 2004 | B2 |
6841240 | Gorny et al. | Jan 2005 | B2 |
7229680 | Crompton | Jun 2007 | B1 |
20010008039 | Alboom et al. | Jul 2001 | A1 |
20010008672 | Norvell et al. | Jul 2001 | A1 |
20020098329 | Abrams | Jul 2002 | A1 |
20030129353 | Abrams | Jul 2003 | A1 |
20030203152 | Higgins et al. | Oct 2003 | A1 |
20040170799 | Carr et al. | Sep 2004 | A1 |
20050081985 | Abrams | Apr 2005 | A1 |
20050136211 | McGovern et al. | Jun 2005 | A1 |
20050158508 | Abrams | Jul 2005 | A1 |
20050266204 | Abrams | Dec 2005 | A1 |
20050268407 | Abrams | Dec 2005 | A1 |
20060251852 | Abrams | Nov 2006 | A1 |
20070003761 | Miyazono et al. | Jan 2007 | A1 |
20070022548 | Abrams | Feb 2007 | A1 |
20070026189 | Abrams | Feb 2007 | A1 |
Number | Date | Country |
---|---|---|
E 93 557 | Aug 1988 | AT |
E 135 427 | Aug 1996 | AT |
606651 | Feb 1991 | AU |
653994 | Oct 1994 | AU |
0506601 | Mar 1996 | BE |
757595 | Apr 1967 | CA |
2010076 | Aug 1990 | CA |
1306411 | Aug 1992 | CA |
2064300 | Sep 1992 | CA |
3883517 | May 1994 | DE |
69208910 | Aug 1996 | DE |
19734316 | Feb 1999 | DE |
EP 0506601 | May 1996 | DK |
0122656 | Oct 1984 | EP |
0210304 | Feb 1987 | EP |
0280296 | Aug 1988 | EP |
0351079 | Jan 1990 | EP |
0506601 | Sep 1992 | EP |
0685014 | Jun 1997 | EP |
0913271 | Oct 1998 | EP |
0989227 | Mar 2000 | EP |
2543984 | Oct 1984 | FR |
2659094 | Sep 1991 | FR |
2784619 | Oct 1998 | FR |
2846202 | Apr 2004 | FR |
1171296 | Nov 1969 | GB |
1466271 | Dec 1973 | GB |
2065031 | Dec 1979 | GB |
2126951 | Sep 1983 | GB |
2214869 | Sep 1989 | GB |
0506601 | Sep 1992 | GB |
55104 | Apr 1984 | IE |
0329787 | Aug 1993 | IT |
24637BE96 | Jun 1996 | IT |
55079143 | Jun 1980 | JP |
56-147171 | Nov 1980 | JP |
356058824 | May 1981 | JP |
56107080 | Aug 1981 | JP |
56108565 | Aug 1981 | JP |
56141877 | Nov 1981 | JP |
358062027 | Apr 1983 | JP |
359115885 | Jul 1984 | JP |
S61-146368 | Jul 1986 | JP |
64-61299 | Mar 1989 | JP |
5-201196 | Aug 1993 | JP |
08-267625 | Oct 1996 | JP |
2001270019 | Oct 2001 | JP |
220373 | Sep 1999 | KR |
2003063833 | Jul 2003 | KR |
306099 | Jun 1989 | NO |
62640 | Jul 1993 | TW |
WO 7901146 | Dec 1979 | WO |
WO 8901829 | Mar 1989 | WO |
WO 9009289 | Aug 1990 | WO |
WO 9419530 | Sep 1994 | WO |
WO 0209925 | Feb 2000 | WO |
WO 0207959 | Jan 2002 | WO |
WO 02058854 | Dec 2002 | WO |
WO 03031083 | Apr 2003 | WO |
WO 2004005023 | Jan 2004 | WO |
WO 2004005413 | Jan 2004 | WO |
WO 2004005600 | Jan 2004 | WO |
WO 2005035235 | Apr 2005 | WO |
WO 2005118948 | Dec 2005 | WO |
886259 | Apr 1990 | ZA |
922154 | Feb 1993 | ZA |
Number | Date | Country | |
---|---|---|---|
20040055692 A1 | Mar 2004 | US |
Number | Date | Country | |
---|---|---|---|
60403992 | Aug 2002 | US | |
60405473 | Aug 2002 | US |