Patent Application
20060159891
The present invention has to do with a process for manufacturing mechanically embossed synthetic surface coverings and the products obtained thereby. More particularly, the invention relates to floor coverings, which are mechanically embossed and processed to create selectively embossed surface areas, thereby creating products having a more realistic appearance including different gloss levels. These appearances include, for example, ceramic tile, stone, brick, sandstone, cork, wood, and in some embodiments textured lines or grout lines there between, as well as combinations thereof such as sandstone and ceramic tile, textured wood and smooth ceramic, cork and wood, and stone or slate in combination with ceramic tile.
Synthetic surface coverings including sheet flooring, wall coverings and tile are employed in residential, commercial and institutional applications where decorative effects, durability and ease of installation and maintenance are important considerations. These surface coverings can be designed to imitate a variety of masonry materials such as ceramic tile, stone and brick or they can be designed with unique combinations of color, particles and other decorative features that are not available in other types of surface coverings. In the current marketplace/consumers are increasingly demanding synthetic surface coverings with improved textural features such as features which realistically imitate not only the textures of materials such as ceramic tile, stone, brick, sandstone, cork, wood and combinations thereof, but also the texture of the grout or mortar which typically is used by a mason or other craftsman to fill the joints between such materials to secure them in their desired position relative to one another.
The surface covering industry has employed mechanical embossing, chemical embossing, combinations of mechanical and chemical embossing, screen printing and other techniques for years in order to obtain design effects and textures which meet consumer demands. In U.S. Pat. No. RE. 33,599 a process is described for obtaining selective matting on synthetic coverings by depositing on an expandable or nonexpandable support substrate (1) a polymer coating which contains at least one first polymerization initiator onto at least a first selected zone and (2) at least one second coating comprised of a crosslinkable monomer which contains at least one second polymerization initiator onto at least a second selected zone. The second zone may encompass at least a portion of the first zone. The first and second initiators are triggered by distinct “spectral zones”. Following pre-gelling, an overall graining operation is carried out over at least a portion of the surface followed by curing the first selected zone and thereby fixing the graining thereon. Then gelling is carried out to cause the graining in the second zone to smooth out. The product has a selectively matted appearance. Other methods of making differential gloss products are described in U.S. Pat. No. 4,298,646 and U.S. Pat. No. 4,491,616.
The surface texture effects of the present invention are obtained by creating relatively deep emboss depths as compared with the shallow graining or dusting techniques employed to obtain the matted or differential gloss effects of the patents noted above. More specifically, the present invention is directed to the realistic imitation in surface coverings not only of the surface texture of a variety of masonry materials such as ceramic tile, stone, brick, sandstone, cork, wood and combinations thereof, but also in some embodiments to the realistic imitation of the surface texture of the grout or mortar in the joints between such materials.
In accordance with the present invention, a novel process is provided for obtaining selective areas of distinctive appearance, e.g., textured grout lines, on the surface of a synthetic surface covering.
Accordingly the invention provides a new and improved method of making a surface covering as claimed in claim 1.
In the method according to the invention at least a portion (preferably the whole portion) of said first photoinitiator used in step (c) migrates into the gelled plastic layer and into the curable coating during and after step (e). In step (g) the softened curable coating is mechanical embossed overall with a specific structure such as that imitating grout. In step (h) said first photoinitiator is activated in an enclosure by means of an appropriate electromagnetic wave or light (for example UV light) so as to cure the curable coating in those areas overlying said printing ink. Upon exiting the activating enclosure, the product enters a fusion oven in step (i) wherein that portion of the curable coating, which does not overlie said printing ink and has thus not been cured, smoothes out such that the grout imitating texture disappears in those areas. The surface of the curable coating which has smoothed out may then optionally be mechanically embossed a second time but now with a structure which imitates for example the texture of stone, wood or the like. Thereafter, the product enters a second activating enclosure in step (k) where the curable coating in at least those unprinted areas thereof is cured by appropriate means (for example by electron beam irradiation) so as to cure the curable coating in those unprinted areas, i.e. those areas which do not overlie said printing ink.
Printing inks without inhibitors may also be printed in a pattern or design directly onto a substrate, which does not have a foamable plastic layer. The resultant product has a flat surface with different textures or appearances including, in some instances, a three-dimensional appearance. In this embodiment, should textured grout lines be part of the pattern or design, the textured grout lines will be flush with the top surface of the product, i.e. without relief.
In a further preferred embodiment, to obtain such a product, a foamable plastic layer containing a foaming agent is applied over a sheet substrate. The combination is then heated to gel the plastic layer without activating the foaming agent. A first printing ink containing a photoinitiator and an expansion inhibitor is then applied in a first pattern on the gelled plastic layer, whereupon a portion of the inhibitor migrates into the gelled plastic layer. Following the printing steps, a first, non-curable coating made from a plastisol or organosol is applied over the entire surface of the gelled plastic layer, including the first and optionally second printing inks. After this, a second, curable coating is applied over the first non curable coating and a portion of the photoinitiator in the printing ink migrates into the coatings. The coatings are then gelled, with or without a cooling step, followed by surface softening through the use of heat. The softened coatings are then mechanically embossed overall with a texture, such as that imitating grout, whereupon the product is cured by exposure within an enclosure to UV light to set the grout texture in those portions of the curable coating overlying the printing ink, which contains a photoinitiator. Upon exiting the UV enclosure, the product enters a fusion and expansion oven wherein that portion of the curable coating which does not overlie the printing ink containing the photoinitiator smooths out such that the grout imitating texture disappears in those areas. Furthermore, those portions of the gelled plastic layer, which do not contain the inhibitor applied with the printing ink, foam and expand. The surface of the curable coating which has smoothed out may then optionally be mechanically embossed a second time but now with a texture which imitates the texture of stone, wood or the like as hereto before described. Thereafter the product enters a second activating enclosure in step (k) where the curable coating in at least those unprinted areas thereof is cured by appropriate means so as to cure the curable coating in those unprinted areas, i.e. those areas which do not overlie said printing ink.
The curable coating preferably comprises an urethane-derived polymer, more preferably, it comprises polyurethane and most preferably it essentially consists in polyurethane.
The curable coating may also further comprise a thermal initiator, which is activated during step k) or even during step i), if a second embossing step is not used.
As will be appreciated by one of ordinary skill in the art, more than one printing ink can be used in the process and product of the invention and each of the inks can optionally contain a photoinitiator and/or an inhibitor. Of course, printing inks, which do not contain a photoinitiator or an inhibitor, can be employed in combination with inks, which do contain a photoinitiator, and/or an inhibitor in order to obtain desired decorative effects.
In still another embodiment of the invention, calendared and/or extruded sheets can be employed in place of the foamable and/or curable coatings as explained in the detailed description below.
In the method according to the invention, photoinitiator means an initiator adapted to initiate curing (for example crosslinking) of the curable coating when activated by a specific electromagnetic energy.
The second photoinitiator may be introduced in the curable coating at any time before the product entering the activating enclosure in step (k). In one embodiment, it is introduced after the product has left the activating enclosure of step (h) i.e. after said first photoinitiator of the printing ink has been activated in step (h). In such a case a liquid photoinitiator may be applied onto the surface of the curable coating.
In another embodiment, said second photoinitiator is introduced in the curable coating prior to step (h) i.e. before the product entering the activating enclosure in step (h). In this embodiment the second photoinitiator is selected among those which are not sensitive to the normal activating conditions of said first photoinitiator, and the activating conditions prevailing in the activating enclosure of step (h) are so adapted as to specifically prevent activating said second photoinitiator. In this embodiment different ways are possible to select a convenient second photoinitiator.
In a first convenient way said second photoinitiator is selected among those having a sensitivity to an activating energy which is higher than the energy necessary to activate said first photoinitiator.
Another convenient way consists in selecting said first photoinitiator among those which are sensitive to a first range of electromagnetic radiation and selecting a second photoinitiator which is sensitive to another range of electromagnetic radiation but not to said first range of electromagnetic radiation.
In a still further embodiment of the method according to the invention said second photoinitiator is selected among those having a migration time into said surface area of the curable coating greater than the migration time of said first photoinitiator into said surface area of the curable coating.
In the embodiments just described the second photoinitiator may be introduced in the curable coating by any convenient means. A particularly convenient means consists in applying said second photoinitiator as a liquid onto the whole surface of the curable coating for example by brushing, painting or spraying. Liquid solutions of said curable photoinitiator are especially preferred.
The activation of the photoinitiators in steps (h) and (k) is advantageously executed by means of electromagnetic radiations. Röntgen radiations are convenient. Ultra violet radiations (UV radiations) are preferred.
In a preferred embodiment of the method according to the invention it is preferred to select a curable coating, which is essentially free from any thermal curing or crosslinking initiator. More preferably, the curable coating is substantially free from any thermal curing or crosslinking inititiator.
Referring to
A clear, non-curable polymeric coating is next applied over the entire surface of the gelled plastic layer including the first and second printing inks. A second, curable coating is then applied over the non-curable coating.
The photoinitiators residing in the first and second printing inks subsequently migrate into the curable coating, which has been applied over the non-curable coating and the inks. The photoinitiators must be chosen so that the rate at which they will migrate from the printing inks into the curable coating is compatible with the speed of the overall process of making the surface covering. The combination of substrate, plastic layer, first and second printing inks, and non curable and curable coatings is then heated to gel the curable coating. The surface of the both coatings is then softened by heat whereupon the softened both coatings are mechanically embossed with an overall textured roll using conventional techniques. The textured roll preferably imitates the texture of sand, cementitious grout, mortar, cork, terrazzo or the like as hereto before described.
To fix the embossed texture in those areas of the curable coating overlying the first and second printing inks, the curable coating enters an enclosure wherein it is irradiated with an UV light of defined energy and wave spectrum. So the UV photoinitiators of both inks which have migrated into the curable coating are activated resulting in a curing (for example crosslinking) of the curable polymeric coating those areas overlying the first and second printing inks.
The product is then placed into a fusion oven where it is heated to about 170° C. to 220° C. preferably to about 185-195° C. The effect is that those portions of the curable coating which do not overlie either the first or second printing ink will fluidise and relax such that the deformations of the curable coating in these areas attributable to the mechanical embossing by means of the textured roll disappear, i.e. smooth over. Additionally, that portion of the foamable plastic layer which does not underlie the second printing ink containing an inhibitor, foams and expands.
The product may then be subjected to a second mechanical embossing step, again by conventional techniques, wherein another texture such as the natural look of stone, wood or the like, as hereinbefore described, is applied to the surface of the curable coating which has smoothed out.
A solution of a curing photoinitiator is applied onto the surface of the curable coating.
The product is then introduced into another enclosure where it is lighted with an UV light of correctly selected energy and wave spectrum so as to have the UV curing photoinitiator of the curable coating activated, resulting in a curing (for example a crosslinking) of the curable polymeric coating in those areas which are outside the first and second printing inks.
An important feature of the process and product of the present invention is that the entire surface of the product may be initially textured in the first mechanical embossing step without necessitating a special patterned texturing roller controlled in register with the design or decoration of the surface covering. This is because the surface areas of the curable coating which are not fixed after the first mechanical embossing step will be softened during the subsequent fusion and expansion treatment and will become smooth because of heat relaxation of plastic memories as taught in U.S. Pat. No. 3,887,678.
A product having the construction illustrated in FIGS. 2 to 4 is prepared by the process of
A clear, non curable coating 5 (see
A curable coating 7 is then applied over the non-curable coating 5.
After heating both the non curable 5 and the curable coating 7 to gel and soften it, the softened coatings 5,7 are mechanically embossed in a first embossing step with a textured roll to create a first texture 8. The textured curable coating is then subjected to ultra violet light 9 to activate the UV photoinitiators of both inks and thus cure that portion (and only that portion) of the curable coating 7 overlying both ink patterns or designs 3, 4. Thereafter the product is heated in an oven to cause that portion of the coatings 5,7 which does not overlie the printing inks 3, 4 to smooth out so that the textures attributable to the first mechanical embossing step disappear in that portion (see
A solution of a curing UV photoinitiator (not shown) is applied onto the surface of the curable coating 7.
The product is then subjected to ultraviolet light 10 to activate the curing UV photoinitiator and thus cure those portions of the curable coating, which are outside the printing ink areas 3 and 4.
Each component of the product and each step of the process of the invention will now be described with reference to various preferred and alternative embodiments.
The Substrate
The substrate is a relatively flat, fibrous or non-fibrous, backing sheet material, such as a fibrous, felted or matted, relatively flat sheet of overlapping, intersecting fibers. The substrate can, if desired, comprise felts or papers, which are woven or non-woven. It can comprise knitted or otherwise fabricated textile material or fabrics made from cellulose, glass, natural or synthetic organic fibers, or natural or synthetic inorganic fibers, or supported or non-supported webs or sheets made therefrom, or filled or unfilled thermoplastic or thermoset polymeric materials. It can also comprise a compact or foamed layer. These and other substrate base materials are well known in the art and need not be further detailed here.
The Foamable Plastic Layer
The foamable plastic layer, when used, can be comprised of any suitable material known in the art for producing foamed plastic layers on a substrate, but is typically a polyvinylchloride (“PVC”) plastisol, an organosol, a polyolefin, an ionomer, plasticized PVC or thermoplastic rubber. This layer can be pigmented or free of pigmentation. If the layer is pigmented, a color is preferably selected which is the average of the colors of the end product so that the appearance and aesthetics of the product are maintained during its working life. To one skilled in the art, the average color means the color perceived when one looks at a surface from a distance of more than about five feet (about 1.5 m).
The foamable plastic layer may include any of the various PVC resin materials normally used in connection with coating of decorative sheet materials and may specifically include, but are not limited to, those described in U.S. Pat. No. 3,458,337. While a suitable foaming agent or blowing agent as taught by the above-mentioned patent may be used, a blend of azodicarbonamide (“ABFA”) and p.p'oxybis (benzene sulfonyl hydrazide) (“OBSH”) foaming agents can be used instead. Additional conventional ingredients such as stabilizers, foaming or blowing agent catalysts, etc. can be used, of course the catalyst is required if chemical inhibition is required. Although the preferred foamable plastic layer is a PVC homopolymer resin, other vinyl chloride resins can be employed. Other synthetic resins are suitable such as polystyrene, substituted polystyrene (preferably wherein the substituents are selected from the group consisting of alkyl having 1-10 carbons, preferably 1-4 carbons, and aryl having 6-14 carbons), polyolefins such as polyethylene and polypropylene, acrylates and methacrylates, polyamide, polyesters and any other natural or synthetic resin.
The composition of the foamable plastic layer must be compatible with the underlying substrate and the printing inks and, when gelled, must provide a smooth and uniform surface for the first and second printing inks. The composition also must be otherwise compatible with the overall product composition and, therefore, within the principles of this invention. As indicated, it is not essential that a plastisol be used as the foamable plastic layer. Organosols and aqueous latexes are also of use, employing as the dispersing or suspending media, organic solvents and water, respectively, rather than plasticizers as in the case of a plastisol.
The foamable plastic layer is substantially uniformly applied in its liquid state to the underlying substrate by conventional means such as a knife-over roll coater, direct roll coater, rotary screen, draw down bar, reverse roll coater or wire wound bar. The particular means for applying the foamable plastic layer does not relate to the essence of the invention, and any suitable coating means can be employed.
The thickness of the foamable, liquid plastic layer as it is applied to the underlying surface is substantially uniform and is in the range from about 2 to about 30 mils (about 50 to about 765 μm), preferably from about 6 to about 16 mils (about 150 to about 410 μm). The layer can be thicker or thinner as may be required by the particular product application.
Instead of a foamable plastic layer, a plastic layer which does not contain a foaming or blowing agent can be applied to the underlying substrate in the same manner as described above.
Gelling
After the foamable, liquid, plastic layer containing a foaming agent is applied over the substrate, the combination is heated for a period of time and at a temperature sufficient to gel the plastic layer, but not sufficient to activate or decompose the blowing or foaming agent. This can be done in an oven or on a heated chrome drum. If an oven is used for the gelling step, a residence time in the oven from about 0.5 minutes to about 3.5 minutes at an oven temperature from about 120° C. to 160° C. will give good results. If a chrome drum is used, a dwell time on the drum from about 8 seconds to about 30 seconds at a drum temperature of from about 110° C. to about 140° C. will give good results. The higher temperatures are used with shorter residence or dwell times and lower temperatures with longer times. The layer is then cooled to provide a surface suitable for printing. Cooling is generally accomplished by contacting the surface of the foamable, gelled plastic layer (and sometimes the underside of the substrate) with one or more cooling drums. Ambient or chilled water is circulated through the drums. Cooling may be enhanced with the use of fans or blowers. The same gelling process can be employed if the plastic layer does not contain a foaming or blowing agent as will be apparent to those skilled in the art. Also calendaring or extrusion techniques followed by lamination onto a substrate of a sheet of similar formulations as above can be used to prepare the printable layer.
The Printing Inks
In the foregoing preferred embodiment, a first printing ink containing a photoinitiator is applied in a first pattern or design onto the gelled plastic layer. Then, a second printing ink containing a photoinitiator and an expansion inhibitor is applied in a second pattern or design onto the gelled plastic layer. Suitable printing inks include those normally used in the manufacture of surface coverings. These include plastisol, solvent-based systems and water-based systems. Of course, in addition to the first and to the second printing ink, other printing inks which do not contain a photoinitiator or an expansion inhibitor can be applied to obtain design objectives. Furthermore, it is not necessary to employ both the first and second printing inks as long as at least one printing ink with a photoinitiator is employed. Either ink can be employed alone or in combination with other printing inks which do not contain a photoinitiator or an expansion inhibitor. If no foamable plastic layer is employed then inks having an expansion inhibitor are not employed.
The first, second and other printing inks may be pigmented or non-pigmented and may include organic pigments or inorganic pigment particles such as titanium dioxide, iron oxide, carbon black, mica, pearlescent and the like. Decorative reflective particles such as metallics, may also be included as part of one or more printing ink compositions. The types and components of the first, second and other printing inks can be the same or different.
The first and second printing inks contain a photoinitiator. By way of example only, and not by limitation, the following ultraviolet crosslinking initiators may be used in accordance with the present invention: benzophenone, 2-chloro-thioxanthone, 2-methyl-thioxanthone, 2-isopropyl-thioxanthone, benzoin, 4,4′-dimethoxybenzoin, benzoin ethyl ether, benzoin isopropyl ether, benzyldimethylketal, 1,1,1-trichloro-acetophenone, 1-phenyl-1,2-propanedione-2-(ethoxycarbonyl)-oxide, diethoxyacetophenone, and dibenzosuberone. The inks containing the photoinitiators should contain about 1% to about 15%, preferably about 10% by weight of photoinitiator.
The second printing ink also contains an expansion inhibitor. By way of example only, and not by limitation, the following inhibitors may be used in accordance with the present invention: benzotriazole, tolyltriazole, fumaric acid and trimellitic anhydride. The specific expansion inhibitor which is used does not relate to the essence of the present invention and many other suitable and acceptable expansion inhibitors are available to one of ordinary skill in the art.
Printing of the inks onto the gelled plastic layer can be effected by rotogravure, flexigraphic, screen printing, pad or knurled printing, or other printing techniques conventionally employed in making floor or wall covering products.
When the second printing ink is applied to the gelled plastic layer, the inhibitor present in the second printing ink migrates into the gelled plastic layer beneath the second printing ink.
It will be appreciated that in the present invention that one ink, two inks or multiple inks may be used to print patterns or designs on the substrate or on the gelled plastic layer. Each ink may optionally contain a photoinitiator and/or an inhibitor. Of course ink without photoinitiators or inhibitors can be used to obtain design objectives. It will also be appreciated that the order of printing is not critical and is not to be construed as a limitation of the invention. Furthermore, it is to be understood that the print areas of the inks may overlap.
The Non Curable Coating
After the printing inks have been applied to the gelled plastic layer, a liquid, non curable coating is applied over the entire surface of the gelled plastic layer including over the first and second printing inks.
The thickness of the non curable coating as it is applied in its liquid, tacky, ungelled state to the gelled plastic layer and inks is substantially uniform and is in the range from about 80 μm to about 400 μm, preferably from about 100 μm to about 250 μm. The coating can be thinner or thicker as may be required by the particular product application. The non curable coating is applied by conventional means such as described above with respect to application of the foamable plastic layer. The particular means for applying the non-curable coating does not relate to the essence of the invention and any suitable coating means can be employed.
The non-curable coating is preferably a clear (transparent) layer but it can be slightly tinted as long as it remains translucent and allows electromagnetic radiations (preferably UV) penetration. The non-curable coating may also contain solid particulates such as chips, flakes, flitters, etc.
This non-curable coating is essentially free of any thermal curing, crosslinking or polymerisation initiator. In the preferred embodiment, the photoinitiators residing in the first and second printing inks then migrate through that portion of the non curable layer which was applied over the first and second printing inks into the curable coating applied above. The non-curable coating is adhered onto the printed gelled plastic layer by any convenient means known in the art, for example laminating.
The Curable Coating
In the method according to the invention a curable coating is applied onto the non-curable coating and advantageously comprise and preferably consist in polyurethane.
Heating and First Embossing Step
To prepare the coatings for mechanical embossing, both the curable coating and the non-curable coating are softened by heating. The product is passed through an oven maintained at a temperature from about 100° C. to about 160° C., preferably from about 130° C. to about 140° C., for a residence time from about 1 to 5 minutes. A hot air recirculating oven and/or an infrared (“IR”) oven operated at these temperatures is generally employed. The product surface is then softened by heat, preferably by means of an IR oven, to a temperature from about 120° C. to 190° C., preferably 150° C. to 170° C., as measured by a pyrometer, before the embossing rollers nip.
Once the coatings have been adequately softened, they are mechanically embossed by means of a textured roll, which imitates the texture of sand, cementitious grout, mortar or the like as hereinbefore described. The textured roll operates under a pressure that depends upon the degree of texturing desired as is known by a person having ordinary skill in the art.
First Ultraviolet (“UV”) Curing
The product may be cooled before it is UV cured. It is not a requirement but it reduces the fumes in the UV enclosure, which would reduce the UV transference to the product. Once the first embossing step has been completed, the product enters an enclosure where it is subjected to the radiations of a UV lamp to cure that portion of the curable coating overlying the first and second printing inks containing a photoinitiator. This step fixes the embossed texture into the surface areas of the coating disposed over the ink containing the photoinitiator.
The UV curing step can occur in a UV reactor wherein the product is subjected to about 10 to about 150 millijoules per square centimeter (mJ/cm2), preferably about 30 mJ/cm2, at about 20 to about 160 watts per cm of adjustable power using H-type, V-type, or D-type bulbs, preferably H-type bulbs.
Fusion and Expansion
After portions of the curable coating have been cured in the above-described enclosure, the product obtained therefrom is introduced to a fusion oven maintained at a temperature from about 170° C. to about 220° C., preferably about 190° C. The product has a residence time in the oven from about 0.5 to about 3 minutes. A hot air recirculating oven and/or an IR oven operated at these temperatures is generally employed.
Subjecting the product to these temperatures for this period of time fuses the substrate, the plastic layer, the printing inks and the coatings together and foams and expands those portions of the foamable plastic layer which do not underlie the second printing ink which contains an inhibitor. Furthermore, those portions (i.e., surface areas) of the curable coating which were not previously cured, i.e., do not overlie either the first or second printing inks, will relax such that the deformation and texturing in the still curable coating in these areas attributable to the first mechanical embossing step to this portion disappear, i.e. smooth over. More particularly, during this step that portion of the curable coating which has not been cured (crosslinked) during UV exposure undergoes relaxation, which has the effect of smoothing the textured surface, while that portion of the curable coating that has been cured during UV curing retains its textured appearance. This relaxation phenomenon is one that requires the first overall embossing to be conducted at a temperature as low as possible to minimize the plastic component of the mechanical deformation induced in the curable coating by the embossing roll.
Second Embossing Step (Optional)
After being removed from the fusion oven, those portions of the curable coating (now the cured coating) which do not overlie the printing inks and hence have smoothed out, are mechanically embossed a second time by means, known to those of ordinary skill in the art, such as a texture roll, or other conventional means containing textures such as the natural looking texture of stone, wood or the like as hereto before described.
Second Ultraviolet (“UV”) Curing
The product from the Fusion Step (or optionally the Second Embossing Step) may be cooled before it is UV cured for reasons explained hereabove regarding the First Ultraviolet Curing. The product then enters an enclosure where it is subjected to the radiations of a UV lamp to cross-link that portion of the curable coating overlying the unprinted areas. This step fixes the embossed texture into those surface areas of the coating.
The UV curing step can occur in a UV reactor wherein the product is subjected to about 400 to about 1000 millijoules per square centimeter (mJ/cm2), preferably about 600 mJ/cm2, of focused or diffused UV radiation, preferably focused radiation, at about 200 to about 600 milliwatts per cm of adjustable power using H-type, V-type, or D-type bulbs, preferably H-type bulbs. Such a UV reactor is available from 1 ST (Germany).
Use of Calendared or Extruded Layers
As noted above, calendared or extruded sheets can be employed as layers in place of any one or both of the foamable layer and/or curable layer. When a foamable sheet is employed it is formed by calendering or an extrusion die at a temperature below the decomposition temperature of the foaming or blowing agent, or the catalyzed foaming or blowing agent. When a sheet is used in place of the curable layer, it is processed by calendering or an extrusion die under conditions which do not significantly decompose the peroxide, so that it remains a curable layer. When sheet materials are used they are laminated to the underlying surface of the product by employing techniques known by those having ordinary skill in the art.
| Number | Date | Country | Kind |
|---|---|---|---|
| 03101984.7 | Jul 2003 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP04/51286 | 6/29/2004 | WO | 12/30/2005 |
