[0001] This invention relates generally to the metallization of a substrate and more specifically
to a process for coating a substrate with a specular metallic coating using electron
beam curing as one step in the process.
[0002] Various processes are known for the metallization of a substrate surface in web or
sheet form. One such process involves the lamination of a thin metal foil to a substrate
by the use of aqueous or non-aqueous solvent based adhesives. This process is commonly
used for the metallization of paper or board and the most common metal used is aluminum
foil. The thinnest commercially available foils have a thickness of 7 to 9um. The
gloss and finish of the final product depend not on the substrate but on the gloss
and finish given to the foil during the lamination process. This process is disadvantageous
from an economy viewpoint because the price of metal foil is high and a relatively
thick coating is required.
[0003] Another commonly used process is vacuum metallization, wherein vaporized metal is
condensed onto the substrate to be metallized. This procedure must take place in a
vacuum on the order of 10
-4 Torr (1.33x10-2 Pa). It is only at these low pressures that the molecules of metallic
vapor issuing from the evaporation source can reach the web without being blocked
or oxidized by gases. Clearly, this process is well adapted to materials which will
not degas or contain volatile substances such as moisture, plasticizers, monomers
or residual solvents. Thus, the substrate used should typically be coated as the direct
metallization of uncoated paper results in a poor finish. In order to improve the
finish, it is necessary to prevarnish the paper substrate. Good results are obtained
only if the paper is not too absorbent and if the prelaquer is very evenly distributed
on the entire substrate surface.
[0004] Furthermore, when this process is applied to materials that substantially degas,
such as paper and cardboard, vacuum metallization causes a loss of moisture content
and subsequent permanent deformation of the substrate. Moreover, rehumidification
may be required in order to avoid deterioration of the mechanical properties of the
substrate.
[0005] Other processes which have been used in the past for coating surfaces include the
so-called "transfer metallization" process described in U.S. Patent No.4,215,170 to
Oliva. Briefly, this process involves coating a substrate or a transfer agent with
varnish, laminating the substrate and the transfer agent together before the varnish
is dried, drying the varnish and separating the transfer agent from the substrate.
The disclosure of U.S. Patent No. 4,215,170 is hereby incorporated by reference.
[0006] The Patent to Oliva discloses that the transfer agent which is used to carry and
transfer metallizing agent may be either polypropylene, polyethylene, cellulose acetate,
polyvinyl chloride, polyvinylidene chloride, regenerated cellulose and similar materials.
The transfer metallization process sometimes involves a curing of the varnish which
may require from 24 to 26 hours depending upon the ambient conditions. This curing
time between lamination and separation interferes with immediate inspection and further
treatment, such as slitting or printing, of the metallized products.
[0007] The search has continued for improved processes which require substantially less
curing time. This invention was made as a result of that search.
[0008] Accordingly, a general object of the present invention is to avoid or substantially
alleviate the above-mentioned problems of the prior art.
[0009] A more specific object of the present invention is to provide a process for coating
a substrate wherein the drying time after lamination is minimized.
[0010] Another object of the present invention is to use electron beam curing in the metallization
process in order to substantially reduce drying time in the final product.
[0011] Other objects and advantages of the present invention will become apparent from the
following summary of the invention and description of its preferred embodiments.
[0012] The present invention provides a process for coating a substrate with a specular
metallic coating and comprises:
(a) coating a transfer agent with a metallic coating;
(b) coating a portion of at least one of the substrate and the coated transfer agent
with varnish;
(c) laminating the substrate and the transfer agent together before the varnish is
cured;
(d) curing the varnish by using electron beam curing; and
(e) separating the transfer agent from the substrate.
[0013] The varnish coating may be applied to the entire surface or be selectively applied
by gravure printing or the like.
[0014] The metallic film provides the substrate with the appearance of a specular metallic
finish. The transfer agent may be reused in subsequent processes. Furthermore, the
coating and laminating steps may be carried out simultaneously.
[0015] The accompanying drawing is a flow diagram of the metallization process in accordance
with the present invention.
[0016] The instant invention is directed to the process for the production of a metallic
coated substrate through use of an electron beam curing technique. A transfer agent
that has a glossy polished surface is metallized in a vacuum chamber. The transfer
agent may be finely finished or may have a structured surface. The surface of the
final product will be a replica of the surface of the transfer agent. The adhesion
of the evaporated metal must be low and in particular less than that of the varnish
to be employed. Suitable transfer agents include untreated polypropylene, polyethylene,
polyvinyl chloride, regenerated cellulose, polyamide and release coated polyester
films. Such transfer agents are disclosed in detail in U.S. Patent No. 4,215,170.
[0017] The transfer agent is metallized by any known technique such as vacuum metallization,
chemical deposition or any other coating process. Suitable metals for deposition include
aluminum, copper, silver, nickel, thin gold, their alloys and other vaporizable metals.
The metal deposited will have a thickness of generally less than about 100OR (0.1µm),
typically less than about 500Å (0.05pm), and preferably less than about 200Å (0.02µm).
The quantity of metal deposited may be monitored by optical or resistance measurements.
The variation of metal thickness across the width of the web should not fluctuate
over too wide a range so that the final product will appear to have a homogeneous
metallic surface.
[0018] The substrate which is to be coated with the metallic film may be in a web or sheet
form and have a rough or smooth surface. Suitable substrates include any sheet material
such as paper, cardboard, wood, leather and other fabrics.
[0019] Next a substrate is completely coated with varnish or selectively coated with varnish
through use of method such as rotogravure, or lithography, flexography or other coating
methods and the transfer agent is laminated to the substrate.
[0020] For some of the applicable coating processes, and in particular, for coating by the
rotogravure process, the varnish is reduced with suitable solvents to create a predetermined
viscosity for application with the coating equipment. In such cases, a drying step
is added to the process to evaporate the solvents after application of the varnish.
The varnish performs different functions during the transfer operation. The varnish
serves to level and smooth the surface of the substrate. The coating of the varnish
may be applied over the metal deposited on the transfer film or on the substrate.
It is also possible to use the laminating press to control directly the amount of
varnish deposited.
[0021] The optimum amount of varnish that may be applied is readily determined by those
skilled in this art. This amount varies depending upon the viscosity of the varnish,
the degree to which the varnish is reduced with solvents, the pressure used during
the lamination step, the hardness of the pressure rolls, and the porosity and surface
irregularities of the substrate.
[0022] As noted above, when the varnish is reduced with a solvent, an additional station
for drying is necessary to remove the solvent before lamination.
[0023] After the varnish is coated on the metallized surfaces or the substrate, a laminating
step takes place before the varnish cures. The lamination is preferably carried out
under slight pressure without heating the laminating rollers. The varnish will adhere
to the metallized surface and will assume the surface characteristics on the transfer
agent.
[0024] After lamination, the complex formed by the transfer agent and the substrate is passed
through an electron beam curing apparatus as described below. After curing, separation
takes place. This step may take place immediately after curing due to the inherent
advantages of the electron beam curing technique.
[0025] Separation substantially immediately after lamination is a great improvement over
previous metallization processes which require long curing times. Immediate delamination
allows immediate inspection of the final metallized product.
[0026] The transfer agent and substrate may be separated onto two separate rollers. After
separation, the transfer agent may be reused numerous times, which is economically
advantageous.
[0027] The finished product comprises a substrate which has a smooth specular metallic coating
which appears to be continuous and smooth. This transfer technique may also be applied
in cases where the varnish is deposited only on selected surfaces. Thus, only certain
portions of the substrate would have a metallic appearance.
[0028] The coated substrate may also then be fed through additional printing stations rather
than immediately rewound. The advantages of immediate curing are greatly utilized
in such an instance. The advantages of immediate curing are particulary important
if the printing of the varnish is done on the substrate in selective patterns, since
printing in registration with those patterns can immediately be accomplished at the
subsequent print stations.
[0029] The final product may be subject to various other processes such as cutting, embossing,
die-stamping, slitting, lacquering and printing. These latter operations require usual
techniques such as offset, rotogravure, flexography, silk screen and others which
are all well-known to those skilled in this art.
[0030] The process and product of the instant invention will now be described in detail
with reference to the figure.
[0031] The figure illustrates a block diagram of the process of the instant invention. Patent
No. 4,215,170, which is incorporated herein by reference, differs in several important
respects as will be described below. Transfer agent 20 is a plastic film which is
preferably untreated polypropylene, or polyethylene polyester or polyvinyl chloride,
and must be finely finished since it will impart the final surface to the metallized
portions of the final product. The most efficient form of production of metallic coated
surfaces occurs when transfer agent 20 is in the form of an elongated web of material
which may be fed by roller means in accordance with the techniques described in U.S.
Patent No. 4,215,170.
[0032] The transfer agent undergoes the step of metallic deposition at step 22 in accordance
with the method of metallization described in detail in U.S. Patent No. 4,215,170.
Briefly transfer agent 20 is fed into a conventional vacuum chamber where a metal
such as aluminum is deposited upon the transfer agent. While thicker metallic coatings
may be desirable for some applications, the resultant metallic film on the transfer
agent preferably has a thickness of approximately 100Å to 500i (0.01 to 0.05pm) and
this extremely small thickness permits minimal use of metallic materials yet upon
conclusion of the process gives the appearance of a completely metallized and continuous
metal surface.
[0033] Substrate 24, the composition of which has been described above, may be in web or
sheet form and have a rough or smooth surface. The substrate is completely coated
or selectively coated with varnish at predetermined locations with gravure, lithography,
flexography or other printing processes at step 26.
[0034] As noted above, lithographic and other forms of printing require the addition of
reducing solvents to the varnish, in which case additional drying stations may be
necessary for removal of the solvents prior to lamination.
[0035] The selectively coated substrate 24 and the transfer agent are laminated at step
28. More particularly, the respective webs of substrate 24 and transfer agent 20 are
brought together in face-to-face relationship between a pair of rollers and pressure
is applied to laminate substrate 24 to transfer agent 20. The pressure required and
the types of rollers used for lamination are described in U.S. Patent No. 4,215,170.
[0036] Subsequent to lamination the varnish is cured at step 30. In U.S. Patent No. 4,215,170,
curing was allowed to occur naturally in approxinmately 24 hours or the curing was
speeded up by the application of heat or the exposure to radiation. Each of these
curing methods required at least a minimal interval between lamination and separation,
thus delaying processing of the final product. The instant invention eliminates this
disadvantage. More particularly, the electron beam curing apparatus shown in block
diagram form at 30 can be of the type manufactured by Energy Sciences, Inc., 8 Gill
Street, Woburn, Massachusetts 01801. This apparatus operates on the principal that
when accelerated electrons penetrate into material they lose speed and transfer their
energy into the material to be treated. The transferred energy excites molecules and
forms a cloud of secondary electrons and free radicals which initiate chemical chain
reactions in specific materials. There are two major applications of electron beam
treatment, the simplest involves cross-linking and vulcanization, i.e., bonding between
adjacent polymer chains and the second involves electron initiated free radical polymerization.
[0037] The electron beam curing apparatus with which we are here concerned consists of several
main elements.
[0038] The source of the electrons is a heated filament, the cathode. From here the electrons
are accelerated, in vacuum, towards an electron transmissible window, which represents
a grounded anode. A high voltage potential applied between the cathode and the anode
accelerates the emitted electrons close to the speed of light.
[0039] The window, a thin metal foil, separates vacuum in the accelerator from atmospheric
pressure in the treatment zone. The acceleration is done in an evacuated environment
to avoid collisions with gas molecules and to prevent cathode oxidation.
[0040] There are two different types of industrial electron accelerators. An earlier design
utilizes a pencil-shaped beam of electrons from a point source which is accelerated
through a multistage accelerator tube and then scanned by an electromagnetic field
through the window over the width of the product to be treated. This type of equipment
is normally used for applications above 300 kV. Later designs, based on a linear cathode,
generate a curtain of electrons over the entire product width without the need of
scanning the beam. The electron beam curing apparatus discussed above is described
in a 1979 publication of Energy Sciences Incorporated entitled "ELECTRO CURTAIN".
[0041] With the electron beam curing process described above, the varnish coating is cured
by exposure for a few milliseconds to the curtain of electrons without the use of
heat. Since the product is completely, and essentially instantaneously cured, it is
immediately available for further processing.
[0042] A slight heat build-up due to the energy transfer of the electrons and the chemical
action can be observed. Normally, the heat build-up will not exceed a few degrees
depending on the curing dose and the thickness of the reactive layer. Thus the equipment
for electron beam curing can be described as a "cold oven" in which the reaction is
initiated by the creation of free radicals by high energy electrons rather than by
thermal effects.
[0043] The particular dose or treatment level required to cure a particular product depends
on the type of material being cured and the thickness of the material.
[0044] Typically, a dose of between 1 and 6 megarads will be used, depending on the material
and thickness of the varnish or adhesive, as well as the substrate and the transfer
agent. Typically also, the voltage of the beam using the equipment described depends
on the thickness of the substrate that the beam is required to penetrate. Therefore
it is preferable to cure through the transfer agent or film, since it is thin and
consistent, rather than through the substrate, which is coarse and inconsistent in
thickness.
[0045] The present invention is further illustrated by the following examples. All particulars
and percentages in the examples, as are those in the specification and claims, are
by weight unless otherwise specified.
EXAMPLE 1
[0046] A varnish of the following composition:

having a viscosity of 24 seconds measured with a cup (Ford Nr. 4) is printed on a
30 micron thick transfer agent of untreated biaxially oriented polypropylene film
which has been vacuum metallized prior to the varnish coating.
[0047] The transfer agent is laminated at a speed of 40 to 50 meters/minute with a 80 gr/sqm
woodfree coated paper substrate and passed under the electron beam of the unit described
hereinabove. The varnish is polymerized and the transfer agent and the substrate are
immediately delaminated.
[0048] The transfer agent is clean and may be reused in the process. The metallized finished
product is dry, has a specular surface, and can immediately be subjected to further
processing, if desired.
EXAMPLE 2
[0049] A varnish designated CD 4336-51 (Lord Corp.) having a viscosity of 87 seconds in
a number 2 Zahn cup, is substituted for the varnish composition given in Example 1
in the procedure described in Example 1. A dose of 2 Mrad electron beam radiation
is used to cure the CD 4336-51 varnish.
EXAMPLE 3
[0050] The preparation of a metallized substrate in register is performed on a six color
gravure press which has been installed with a laminating/electron beam/ delaminating
unit between the first and second printing units.
[0051] A varnish of the following composition:

is printed in a design at a speed of 50 meters/minute on a woodfree coated substrate
and dried in an oven at 100
oC, but not cured. At the end of the drying step, the varnish-printed paper is laminated
with a vacuum metallized oriented polyethylene film (transfer agent), passed under
the electron beam in order to polymerize the varnish, and delaminated immediately
thereafter, before entering the second printing unit.
[0052] The metallic design is overprinted in-line with a yellow transparent ink to give
a specular gold effect.
EXAMPLE 4
[0053] In the process of Example 3, a varnish of the following composition is used:

[0054] This varnish, as prepared, has a viscosity of 21 seconds in a number 2 Zahn cup.
The varnish is printed on a woodfree coated paper as described above and then dried
in an oven at about 70°C to increase the viscosity of the varnish to about 90 Pascal-seconds
(Pa's). The dried, but uncured, varnish-printed substrate is laminated to the metallized
transfer agent, passed through the electron beam curing unit where the varnish is
cured with a dose of 2 Mrad, and immediately delaminated to separate the now metallized
substrate from the reusable transfer agent. As the substrate is separated from the
transfer agent, it proceeds directly into the second print unit where the metallized
design is overprinted, in substantial registry, with a yellow ink to give a specular
gold effect.
EXAMPLE 5
[0055] A varnish of the following composition:

having a viscosity of 24 seconds in a number 2 Zahn cup is printed in a design by
the same procedure as described in Examples 3 and 4. This varnish is dried, however,
to achieve a viscosity on the order of 7 Pa's prior to entering the laminating/electron
beam curing /delaminating unit. Again, a 2 Mrad dosage of electron beam radiation
is used to substantially instantaneously cure the varnish so as to permit immediate
delamination of the reusable transfer agent and uniterrupted travel of the metallized
substrate into the second printing unit. At the second printing unit, the metallized
design is overprinted, in substantial registry, with an orange ink to give a specular
copper effect.
EXAMPLE 6
[0056] A serigraphic impression is realized with an ink of the following composition:

[0057] The printing is performed on a coated board of 120 grams/sqm. The printed substrate
is immediately laminated with a vacuum metallized oriented polypropylene film and
polymerized with the electron beam curing unit. The delamination takes place immediately
after the drying operation.
EXAMPLE 7
[0058] A varnish designated KC80-384 (Sun, GPI) is printed by lithography on a coated board.
The printed substrate is immediately laminated with a vacuum metallized, biaxially
oriented, untreated polypropylene film and passed through the electron beam curing
unit where it is cured with a dose of 3 Mrad electron beam radiation. The polypropylene
film is immediately delaminated from the coated board.
[0059] 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, however, is not to be construed as limited to the particular
forms disclosed, since these are to be regarded as illustrative rather than restrictive.
Variations and changes may be made by those skilled in this art without departing
from the spirit of the invention.
1. A process for the metallization of a substrate employing a reusable transfer agent
comprising the steps of;
depositing on said transfer agent a film of metal particles of the order of magnitude
of substantially less than 1000 R (0.1pm) in thickness,
coating a portion of at least one of said substrate and said metallized transfer agent
with electron beam-curable varnish,
laminating said substrate and said transfer agent together before said varnish is
cured,
curing said varnish substantially instantaneously with electron beam radiation and
separating said transfer agent from said substrate immediately after said curing step
is completed.
2. The process as claimed in claim 1 wherein said transfer agent is a resin selected
from the group consisting of polypropylene, polyethylene, polyvinyl chloride, polyamide
and regenerated cellulose.
3. The process as claimed in claim 1 or claim 2 wherein said metal particles are of
metals selected from the group consisting of aluminum, silver, gold, copper, nickel,
tin and platinum and alloys of said metals.
4. The process as claimed in any preceding claim wherein said varnish is coated in
a particular design not covering the entire surface of said substrate.
5. The process as claimed in any preceding claim wherein said substrate is selected
from the group consisting of paper, cardboard, wood, leather and plastic.
6. The process as claimed in any preceding claim wherein said electron beam curing
step polymerizes said varnish.
7. A metallized substrate formed by the process of any preceding claim.
8. A process for producing a specular metallic coating on at least predetermined portions
of a substrate, the process comprising the steps of:
depositing a thin film of metal particles on a transfer agent;
coating said at least a predetermined portion of at least one of said substrate and
said metallized transfer agent with an electron beam-curable varnish;
laminating said substrate and said metallized transfer agent together before said
varnish is cured to form a laminated product;
exposing said laminated product to electron beam radiation so as to substantially
instantaneously cure said varnish;
delaminating said transfer agent from said substrate substantially immediately after
performing said step of exposing; and
printing in substantial registry with the metallic coating on said at least a predetermined
portion of said substrate.
9. The process as claimed in claim 8 wherein said coating step and said printing step
are performed by use of a gravure press.
10. The process as claimed in claim 8 or claim 9 wherein said thin film of metal particles
has a thickness of the order of magnitude of substantially less than 1000 i (0.1pm).
11. The process as claimed in any one of claims 8 to 10 wherein said transfer agent
is a resin selected from the group consisting of polypropylene, polyethylene, polyvinyl
chloride, polyamide and regenerated cellulose.
12. The process as claimed in claim 11 wherein said transfer agent has a structured
surface, thereby causing said metallic coating to be formed as a replica of the structured
surface of said transfer agent.
13. The process as claimed in any one of claims 8 to 12 wherein prior to said exposing
step said laminated product is -oriented so that the transfer agent side is first
exposed to the source of electron beam radiation.
14. The process as claimed in any one of claims 8 to 13 further comprising the steps
of:
diluting said varnish with a solvent prior to said coating step; and
evaporating at least a portion of said solvent so as to increase the viscosity of
said varnish prior to said laminating step.
15. The process as claimed in claim 14 wherein said evaporating step comprises drying
said varnish in an oven at an elevated temperature.