Coating processes – Coating remains adhesive or is intended to be made adhesive – Pressure sensitive adhesive
Reexamination Certificate
2001-11-29
2003-11-25
Bareford, Katherine A. (Department: 1762)
Coating processes
Coating remains adhesive or is intended to be made adhesive
Pressure sensitive adhesive
C427S505000, C427S516000, C427S561000, C427S566000, C427S208400, C427S428010
Reexamination Certificate
active
06652908
ABSTRACT:
BACKGROUND OF THE INVENTION
EP 0 622 127 B1 discloses that, by way of a roller, pressure-sensitive, solvent-free adhesive coats are placed onto a substrate. The application device used comprises single-manifold or multimanifold dies.
Owing to an applied difference in speed between the coated roller or the receiving substrate, the premetered adhesive film is reduced in its thickness, so that thin pressure-sensitive adhesive coats can be transferred to substrates.
A disadvantage of the known method is that pressure-sensitive adhesive coats can be received from smooth, untreated rollers only by nonrelease-coated substrates, or that the roller coated with the pressure-sensitive adhesive must exhibit a release effect, which can be produced by way of a fluorocarbon coat or Teflon coat. This release coat diminishes in the course of its lifetime and is sensitive to external influences such as wear, dirt, and mechanical damage. Furthermore, release rollers produced with fluorocarbon or Teflon coatings lack sufficient release properties with respect to acrylate hot-melt pressure-sensitive adhesives in the case of machine stoppages, so that the result is not a robust process without laborious cleaning operations of the coated roller in conjunction with down times.
Likewise known from the prior art is the gravure roller coating method, with hot-melt adhesives metered by way of a die.
The disadvantage of the gravure roller method, however, is that, depending on the type of hot-melt adhesive, the structure of the engraved roller surface is transferred to the adhesive film when the coat of adhesive is transferred to a substrate. A further disadvantage of the gravure roller coating method is that, at relatively high coating speeds, full discharge of the engraved structures is not possible and there may therefore be uneven application of adhesive. With release-coated substrates, moreover, the reception of the adhesive film by structured roller surfaces is again very difficult.
It is an object of the present invention to provide a method of producing a solvent-free pressure-sensitive adhesive coating on substrates, especially release-coated substrates, which avoids the disadvantages of the prior art.
SUMMARY OF THE INVENTION
The invention accordingly describes a method of producing a coating of solvent-free pressure-sensitive adhesive systems on substrates, especially release-coated substrates, in which
a fluid film is applied to a rotating roller by means of a fluid applicator, the pressure-sensitive adhesive system is applied in one or more layers to the fluid film by means of an adhesive applicator, so that the fluid film is located between roller and pressure-sensitive adhesive system, and
the roller is contacted with the substrate, so that the pressure-sensitive adhesive system is transferred from the roller to the substrate (release-coated and nonrelease-coated).
DETAILED DESCRIPTION
The contacting of the substrate takes place in particular by way of a second roller. Substrates used include papers, films, nonwovens and release-coated materials such as release papers, films, and the like.
The second roller, also referred to as the contact roller, preferably has a rubber coating and is pressed against the roller with a linear pressure of preferably from 50 to 500 N/mm, in particular at from 100 to 200 N/mm. The contact roller preferably has a Shore hardness (A) of 40-100, in particular a Shore hardness of 60-80 shore (A).
The substrate is preferably brought into contact with the roller in such a way that the speed of the roller surface coincides with that of the substrate. Where, however, it is intended that a reduction in thickness should take place along with the reception of the adhesive film, the substrate may also have a higher speed.
In a first advantageous embodiment, the roller is a steel roller, a chrome-plated steel roller, a rubber roller or a silicone rubber roller and or is manufactured from elastic material. Furthermore, the roller may be smooth or may have a slightly structured surface. The smooth roller may preferably have a chrome coating, Optionally, the chrome-plated steel roller may possess a high-gloss-polished surface with a roughens R
z
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The coating roller may also, however, be rubberized, preferably with a rubber hardness of from 40 to 100 shore (A), in particular with a hardness of 60-80 shore (A). The roll coating may, in accordance with the prior art, comprise ethylene-propylene terpolymer (EPDM), VITON® fluoroelastomer or silicone rubber, or other elastic materials.
It has also proven advantageous for the roller to be temperature-controllable, preferably in a range from −10° C. to 200° C., with very particular preference from 2° C. to 50° C.
The placement of the pressure-sensitive adhesive system onto the roller takes place in particular by means of a single-channel or multichannel nozzle or a slot die. The fluid-laden roller is preferably coated contactlessly with the adhesive film emerging from the die. The distance of the die from the roller may be preferably from 0 to 60 mm, in particular from 1 to 10 mm.
Furthermore, the fluid applicator should also be temperature-controllable, in order to bring agents which are present in but insensitive to the adhesive formulation to temperatures associated with desired fluid properties.
The fluid may be wiped on or carried on; it is, however, also possible for the fluid to be brought onto the roller contactlessly, by spraying, for example.
In another advantageous embodiment of the invention, the pressure-sensitive film is crosslinked prior to transfer to the substrate, in particular by means of electron beams, UV rays or a combination of the two techniques.
Typical exposure means employed in the context of the inventive embodiment of the method are linear cathode systems, scanner systems, or multiple longitudinal cathode systems, where the equipment in question comprises electron beam accelerators.
The acceleration voltages are situated in the range between 40 kV and 350 kV, preferably from 80 kV to 300 kV. The output doses range between 5 and 150 kGy, in particular from 20 to 90 kGy.
As UV crosslinking units it is possible in particular to employ two medium-pressure mercury lamps each with an output of 120 W/cm or one medium-pressure mercury lamp having an output of 240 W/cm. The doses set are preferably from 10 to 300 mJ/cm
2
.
The pressure-sensitive adhesive film may be crosslinked thermally, by way of the temperature of the coated roller, and it is also possible for thermal crosslinking to be used supplementarily.
The fluid film is preferably water and/or distilled water, with or without additions such as alcohol, wetting agents and/or agents insensitive to the adhesive formulation, such as plasticizers or liquid aging inhibitors.
To achieve uniform wetting, the surface tension of the fluid should be lower than the surface tension of the roller that is to be wetted.
As the pressure-sensitive adhesive system, use is made in particular of acrylic, natural rubber, synthetic rubber or EVA adhesives.
Examples of low molecular mass acrylic hotmelts employed include copolymers of (meth)acrylic acid and esters thereof having from 1 to 25 carbon atoms, maleic, fumaric and/or itaconic acid and/or their esters, substituted (meth)acrylamides, maleic anhydride, and other vinyl compounds, such as vinyl esters, especially vinyl acetate, vinyl alcohols and/or vinyl ethers.
The acrylic hotmelts may further be blended with one or more additives such as aging inhibitors, crosslinkers, light stabilizers, ozone protectants, fatty acids, resins, plasticizers, and accelerators.
Furthermore, they may have been filled with one or more fillers such as fibers, carbon black, zinc oxide, solid microbeads, silica, silicates, and chalk, the addition of blocking-free isocyanates also being possible.
In the case of rubber/synthetic rubber as a starting material for the adhesive, further variation possibilities exist, whether said material is from the group of the natural rubbers or the synthetic rubbers or whether it
Guldbrandsen Lars
Hirsch Ralf
Möller Dieter
Neuhaus-Steinmetz Hermann
Schulz Stefan
Bareford Katherine A.
Norris & McLaughlin & Marcus
tesa AG
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