Field of the Invention
[0001] The invention relates to a process for laser marking of a liquid crystal film. The
invention further relates to a liquid crystal film obtained by this method and to
its use in optical, decorative or security applications, for optical information storage
or the preparation of liquid crystal pigments.
Background and Prior Art
[0002] Liquid crystal polymer (LCP) films comprising polymerised liquid crystal material
can be produced with various properties which are especially suitable for optical,
decorative or security applications and for optical information storage.
[0003] Thus, reflective LCP films with an angular dependant reflection colour can be generated
from cholesteric liquid crystal mixtures, or nematic LCP films can be used in applications
such as hot stamping foils. These films are usually prepared by coating a thin layer
of a polymerisable LC mixture onto a substrate, aligning the mixture into uniform
orientation and polymerising the mixture to fix the structure.
[0004] For several applications it is desired to add further patterns or images to the LCP
film. In prior art this is usually achieved by the use of two or more steps of photopolymerisation,
e.g. by polymerisation under different conditions and/or using photoisomerisable,
photoorienting or thermochromic materials that change their properties between the
different curing steps, in combination with photomasking techniques and/or photopolymerisation
with linear polarised light.
[0005] Another method to provide a visible marking in an LCP film is reported in US 6,207,240.
This reference describes an effect coating of a cholesteric liquid crystal polymer
(CLCP) with viewing angle dependent reflection colour which further comprises absorption
type pigments exhibiting a specific absorption colour. A marking, such as a symbol
or text, is generated in the CLCP coating by laser irradiation. The laser radiation
carbonises the CLCP material in the irradiated area. As a result, the colour of the
substrate on which the CLCP is coated, or the colour of absorption pigments incorporated
into the CLCP, become visible in the irradiated area. However, the method as described
for example in US 6,207,240 is limited to cholesteric LC materials and requires high
powered lasers to carbonize the material such that the markings are visible.
[0006] It is an aim of the present invention to provide a process for marking a liquid crystal
film that does not have the drawbacks of prior art, yields markings with good visibility,
is time and cost-effective, does not have the limitations of the prior art materials,
can be applied to a broad variety of substrates, surfaces and objects, and allows
a fast, reliable and economic fabrication even at large scales.
[0007] A further aim of this invention relates to a liquid crystal film comprising a marking
obtained by the process according to this invention, which is particularly suitable
for optical, decorative, security, authentification or identification applications.
[0008] A further aim of this invention is to provide an advantageous use of a marked liquid
crystal film according to this invention.
[0009] Further aims of this invention relate to security, authentification or identification
markings or devices and optical data storage devices, which are difficult to counterfeit.
[0010] Other aims of the present invention are immediately evident to the person skilled
in the art from the following detailed description.
[0011] The inventors have found that these aims can be achieved by providing a process for
laser marking of a liquid crystal film according to the present invention.
Summary of the Invention
[0012] The invention relates to a process for generating a marking in a liquid crystal film
by laser irradiation, wherein the liquid crystal film comprises a polymerised liquid
crystal material and one or more interference pigments.
[0013] The invention further relates to a liquid crystal film with a laser marking obtained
by the process as described above and below.
[0014] The invention further relates to the use of a liquid crystal film as described above
and below in optical, decorative, security, authentification or identification applications,
for optical information storage or for the preparation of liquid crystal pigments.
[0015] The invention further relates to a film, marking, thread or device for optical, decorative,
security, authentification or identification purposes, comprising a liquid crystal
film as described above and below or comprising one or liquid crystal pigments prepared
from such a film.
[0016] The invention further relates to documents of value, hot stamping foils, transfer
foils, reflective foils and optical data storage devices, each comprising at least
one film, marking, thread or device according to this invention.
Definition of Terms
[0017] The term 'film' as used in this application includes self-supporting, i.e. free-standing,
films that show more or less pronounced mechanical stability and flexibility, as well
as coatings or layers on a supporting substrate or between two substrates.
[0018] The term 'liquid crystal or mesogenic material' or 'liquid crystal or mesogenic compound'
means materials or compounds comprising one or more rod-shaped, board-shaped or disk-shaped
mesogenic groups, i.e. groups with the ability to induce liquid crystal phase behaviour.
Liquid crystal compounds with rod-shaped or board-shaped groups are also known in
the art as 'calamitic' liquid crystals. Liquid crystal compounds with a disk-shaped
group are also known in the art as 'discotic' liquid crystals. The compounds or materials
comprising mesogenic groups do not necessarily have to exhibit a liquid crystal phase
themselves. It is also possible that they show liquid crystal phase behaviour only
in mixtures with other compounds, or when the mesogenic compounds or materials, or
the mixtures thereof, are polymerised.
[0019] For the sake of simplicity, the term 'liquid crystal material' is used hereinafter
for both liquid crystal materials and mesogenic materials, and the term 'mesogen'
is used for the mesogenic groups of the material.
[0020] The 'director' is the preferred orientation direction of the long molecular axes
(in case of calamitic compounds) or short molecular axis (in case of discotic compounds)
of the mesogens in a liquid crystal material.
[0021] The term 'planar structure' or 'planar orientation' refers to a layer or film of
liquid crystal material wherein the director is substantially parallel to the plane
of the film or layer.
[0022] The term 'homeotropic structure' or 'homeotropic orientation' refers to a layer or
film of liquid crystal material wherein the director is substantially perpendicular
to the film plane, i.e. substantially parallel to the film normal.
[0023] The term 'tilted structure' or 'tilted orientation' refers to a layer or film of
liquid crystal material wherein the director is tilted at an angle of between 0 and
90 degrees relative to the film plane.
[0024] The term 'splayed structure' or 'splayed orientation' means a tilted orientation
as defined above, wherein the tilt angle varies monotonuously in the range from 0
to 90 °, preferably from a minimum to a maximum value, in a direction perpendicular
to the film plane.
[0025] For sake of simplicity, a film comprising liquid crystal material with a tilted,
splayed, low tilted, planar and homeotropic orientation or structure is hereinafter
also referred to as 'tilted film', 'splayed film', 'low tilt film', 'planar film'
and 'homeotropic film', respectively.
Detailed Description of the Invention
[0026] The present invention relates to a way of laser marking a pattern or design into
a liquid crystal polymer film that comprises interference pigments, which are selected
to absorb at least partially the laser energy, like for example the commercially available
Iriodin® LS range of pigments (from Merck KGaA, Darmstadt, Germany).
[0027] The method according to the present invention has significant advantages over prior
art technology. Thus, the use of expensive special materials, curing masks, at least
two stages of photopolymerisation and/or more than one coating process is avoided.
Also, where the current invention implies the usual coating and curing stages for
preparing the polymer film, the manufactured film can simply and quickly be marked
by incorporating a laser stage after the curing stage and before the rewind. The speed
of laser marking is thus not a limiting factor in the speed of film production.
[0028] To prepare a polymer film, the polymerisable liquid crystal material comprising the
laser absorbing interference pigments is typically applied as a thin layer on a substrate,
aligned into uniform orientation, polymerised or crosslinked to fix the orientation
molecules, and optionally the substrate is removed from the polymerised film. A marking
for example in the form of a pattern, design or text is then inscribed into the film
by exposure to laser intensity light. The interference pigments incorporated into
the liquid crystal material are activated by the laser to give rise to the additional
markings. The absorption of energy by the pigment causes a localised heating of the
surrounding liquid crystal material which in turns destroys the optical properties
(reflection of polarised light, birefringence etc.) of the liquid crystal material.
This in turn can be seen as a visible effect in the liquid crystal polymer layer,
namely a loss of angular colour dependence in the case of cholesteric liquid crystal
polymers and a loss of birefringence in the case of nematic liquid crystal polymers.
The effect in nematic materials will be particularly apparent when viewed through
a linear polariser.
[0029] Preferably the polymerisable liquid crystal material is a nematic, smectic, chirai
nematic (cholesteric) or chiral smectic material.
[0030] Preferably, in case of nematic liquid crystal materials, the polymerised material
exhibits planar orientation, although other orientations like for example tilted or
splayed are also possible.
[0031] In a preferred embodiment the polymerisable liquid crystal material is a nematic
liquid crystal material. A film prepared from such a material is transparent when
viewed at normal conditions, but shows a pattern of interference colours when viewed
through a linear polariser against a reflective background or when viewed between
two linear polarisers. The laser marking will thus appear in such a film as a black
marking in the interference pattern of the nematic material when viewed thorugh a
polariser or between two polarisers.
[0032] The above embodiment is particularly suitable for use as false-proof security markings
or security threads on banknotes or documents of value, by which the document is easy
to authenticate when viewed either directly in the case of cholesteric materials,
or, in the case of nematic materials, when viewed through one polariser against a
reflective background or between two polarisers.
[0033] The pigments incorporated into the liquid crystal film are preferably selected from
pearlescent or interference pigment flakes comprising a substrate of e.g. mica, SiO
2, Al
2O
3, TiO
2 or glass that is coated with one or more layers of e.g. titanium dioxide, iron oxide,
titanium iron oxide or chrome oxide or combinations thereof, or flakes comprising
combinations of metal and metal oxide. Further preferred are metal flakes of e.g.
aluminium coated with layers of iron oxide layers and/or silicium dioxide. Particularly
suitable pearlescent pigments are the commercially available Iriodin® pigments, such
as Iriodin LS800, LS820 or LS825, Xirallic® or Colourstream® pigments (from Merck
KGaA, Darmstadt, Germany), or Paliochrome® pigments(from BASF AG, Ludwigshafen, Germany).
[0034] The amount of the interference pigments in the liquid crystal material is preferably
from 0.05 to 30 %, in particular from 0.1 to 10 %, very preferably from 0.5 to 5 %.
[0035] Further additives, like for example absorptive pigments or dyes can also be incorporated
into the films to provide additional effects.
[0036] The laser used for marking the film can be a commercially available laser. The wavelength
of laser irradiation is typically in the range from 150 to 1100 nm. Suitable and preferred
lasers are selected from the group comprising CO
2 lasers, Nd:YAG lasers, frequency-tripled Nd:YAG lasers (355 nm), frequency-quadrupled
Nd:YAG lasers (266 nm) or UV lasers. Preferred UV lasers are excimer lasers, such
as F
2 excimer lasers (157 nm), ArF excimer lasers (193 nm), KrCl excimer lasers (222 nm),
KrF excimer lasers 248 nm), XeCl excimer lasers (308 nm) and XeF excimer lasers (351
nm).
[0037] The lasers have typically an energy density (power) of 0.3 mJ cm
-1 to 50 J cm
-1, preferably of 0.5 mJ cm
-1 to 20 J cm
-1 and particularly 1 mJ cm
-1 to 10 J cm
-1.
[0038] The pulse frequency is typically from 0.1 to 10000 Hz, preferably from 1.0 to 1000
Hz. The pulse length is typically from 0.1 to 1000 ns, preferably from 1.0 to 100
ns.
[0039] The above values should not be taken as exclusive for the inventive process. Other
wavelengths, powers and pulse lengths and frequencies may also be used to produce
the same effect. Operating conditions for different machines will be different from
those stated above and the nature of conditions required will depend upon the size
and definition of the required marking.
[0040] Preferred embodiments of the invention relate to a method wherein
- the liquid crystal material is a nematic material,
- the liquid crystal material is crosslinked,
- the liquid crystal material shows birefringent patterns when viewed between linear
polarisers,
- the interference pigments are selected from the group comprising coated mica, silica
or alumina pigments
- the interference pigments are selected from the group comprising Iriodin® Pigments,
in particular Iriodin® LS800 or LS825 (commercially available from Merck KgaA, Darmstadt,
Germany),
- the laser light has a wavelength of 800 to 1200 nm,
- the laser light has a power of from 50 to 150 W,
- the laser light has a pulse length from 1 to 100 nsec.
[0041] The above described technique can be applied to any LC material.
[0042] The liquid crystal material can be applied onto a substate by conventional coating
techniques like spin-coating or blade coating. It can also be applied to the substrate
by conventional printing techniques which are known to the expert, like for example
screen printing, offset printing, reel-to-reel printing, letter press printing, gravure
printing, rotogravure printing, flexographic printing, intaglio printing, pad printing,
heat-seal printing, ink-jet printing or printing by means of a stamp or printing plate.
[0043] Suitable substrates include films, paper, board, leather, cellulose sheeting, textiles,
plastics, glass, ceramics and metals. Suitable plastic substrates are for example
films of polyester such as polyethyleneterephthalate (PET) or polyethylenenaphthalate
(PEN), polyvinylalcohol (PVA), polycarbonate (PC) or triacetylcellulose (TAC), especially
preferably PET or TAC films.
[0044] In a preferred embodiment the substrate is a metallic or metallised film of e.g.
aluminium. Further preferred are substrates covered by one or more layers of pearlescent
or intereference pigments or liquid crystal pigments, or mixtures thereof, which are
dispersed in a transparent binder.
[0045] The substrate or at least the surface of the substrate covered by the liquid crystal
material is preferably flat, like e.g. a foil, film or sheet, and has preferably a
thickness smaller than 200 µm, in particular smaller than 60 µm, most preferably smaller
than 20 µm.
[0046] The substrate surface is preferably planar, but may also be structured, patterned
and/or have a relief. The shape, structure, pattern and/or relief of the substrate
is preferably adapted to the desired application of the liquid crystal film. Suitable
structuring and patterning techniques are well known to the one skilled in the art,
in particular in the fields of precision engineering and microtechnology, and include
lithography, etching, cutting, stamping, punching, embossing, molding and electron
discharge machining techniques.
[0047] It is also possible to use a reflective substrate comprising a hologram or kinegram,
a holographic layer with an embossed, patterned or structured surface, or a layer
of reflective holographic pigments. Light reflected by higher regions of the structured
surface will interfere with light reflected by lower regions of the structured surface,
thereby forming a holographic image.
[0048] The liquid crystal material may be applied onto one side or on both sides of the
substrate. It may for example be printed onto discrete regions of the substrate to
form a pattern or image, or printed or coated onto the entire substrate to form a
continuous layer or film.
[0049] Preferably the liquid crystal film is prepared by applying a mixture comprising the
liquid crystal material and one or more interference pigments onto the substrate.
The mixture can also be applied as solution, dispersion or emulsion of the liquid
crystal material in a suitable solvent, and the solvent is then evaporated before
or during polymerisation. Preferably a solution is used. The solvent may evaporate
with or without the use of external forces such as heat or reduced pressure.
[0050] The liquid crystal material may additionally comprise a polymeric binder or one or
more monomers capable of forming a polymeric binder and/or one or more dispersion
auxiliaries. Suitable binders and dispersion auxiliaries are disclosed for example
in WO 96/02597. Especially preferred are liquid crystal materials not containing a
binder or dispersion auxiliary.
[0051] The polymerisable liquid crystal material preferably comprises at least one polymerisable
mesogenic compound having one polymerisable functional group (monoreactive compound)
and at least one polymerisable mesogenic compound having two or more polymerisable
functional groups (di- or multireactive compound).
[0052] If di- or multireactive compounds are present in the polymerisable material, a three-dimensional
polymer network is formed and the planar orientation of the LC material is permanently
fixed. A polymer film made of such a network is self-supporting and shows a high mechanical
and thermal stability and a low temperature dependence of its physical and optical
properties.
[0053] By varying the concentration of the di- and multireactive compounds the crosslink
density of the polymer film and thereby its physical and chemical properties such
as the glass transition temperature, which is also important for the temperature dependence
of the optical properties of the optical retardation film, the thermal and mechanical
stability or the solvent resistance can be tuned easily.
[0054] A preferred polymerisable liquid crystal material comprises
- 3 - 60 %, very preferably 5 to 35 % of one or more direactive achiral mesogenic compounds,
- 20 - 90 %, very preferably from 30 to 80 % of one or more monoreactive achiral mesogenic
compounds,
- 0.05 to 30 %, in particular 0.1 to 10 %, very preferably 0.5 to 5 %of one or more
interference pigments,
- 0 to 15 %, preferably 0.5 to 10 % of one or more photoinitiators.
[0055] The polymerisable mesogenic mono-, di- or multireactive compounds used for the present
invention can be prepared by methods which are known per se and which are described,
for example, in standard works of organic chemistry such as, for example, Houben-Weyl,
Methoden der organischen Chemie, Thieme-Verlag, Stuttgart. Typical examples are described
for example in WO 93/22397; EP 0 261 712; DE 19504224; DE 4408171 and DE 4405316.
The compounds disclosed in these documents, however, are to be regarded merely as
examples that do not limit the scope of this invention.
[0058] In the above formulae, P is a polymerisable group, preferably an acryl, methacryl,
vinyl, vinyloxy, propenyl ether, epoxy or styryl group, x and y are each independently
1 to 12 , A is 1,4-phenylene that is optionally mono- di or trisubstituted by L
1 or 1,4-cyclohexylene, v is 0 or 1, Z
0 is -COO-, -OCO-, -CH
2CH
2- or a single bond, Y is a polar group, Ter is a terpenoid radical like e.g. menthyl,
Chol is a cholesteryl group, R
0 is an unpolar alkyl or alkoxy group, and L
1 and L
2 are each independently H, F, Cl, CN or an optionally halogenated alkyl, alkoxy, alkylcarbonyl,
alkoxycarbonyl or alkoxycarbonyloxy group with 1 to 7 C atoms.
[0059] The term 'polar group' means a group selected from F, Cl, CN, NO
2, OH, OCH
3, OCN, SCN, an optionally fluorinated carbonyl or carboxyl group with up to 4 C atoms
or a mono- oligo- or polyfluorinated alkyl or alkoxy group with 1 to 4 C atoms. The
term 'unpolar group' means an alkyl group with 1 or more, preferably 1 to 12 C atoms
or an alkoxy group with 2 or more, preferably 2 to 12 C atoms.
[0060] In case CLC materials are used, these preferably comprise a nematic or smectic host
material and one or more chiral dopants that induce a helical twist in the host material.
The chiral dopants can be polymerisable or not. They can be mesogenic or liquid crystal
compounds, but do not necessarily have to be liquid crystalline.
[0061] Suitable polymerisable chiral compounds can be selected for example from the above
formulae. Suitable non polymerisable chiral compounds can be selected e.g. from the
commercially available chiral dopants R/S 811, R/S 1011, R/S 2011 or CB 15 (from Merck
KGaA, Darmstadt, Germany). Very preferred are chiral compounds with a high helical
twisting power (HTP), in particular compounds comprising a sorbitol group as described
in WO 98/00428, compounds comprising a hydrobenzoin group as described in GB 2,328,207,
chiral binaphthyl derivatives as described in WO 02/94805, chiral binaphthol acetal
derivatives as described in WO 02/34739, chiral TADDOL derivatives as described in
WO 02/06265, and chiral compounds having at least one fluorinated linkage group and
a terminal or central chiral group as described in WO 02/06196 and WO 02/06195. The
amount of chiral dopants in the liquid crystal material is preferably less than 15
%, in particular from 0.01 to 10 %, very preferably from 0.1 to 5 % by weight of the
total liquid crystal material (without solvent).
[0062] Planar alignment of the liquid crystal material can be achieved for example by shearing
the material, e.g. by means of a doctor blade. It is also possible to apply an alignment
layer, for example a layer of rubbed polyimide or sputtered SiO
x, on top of at least one of the substrates. Planar alignment can also be achieved
by rubbing the substrate without applying an additional alignment layer, e.g. by means
of a rubbing cloth or a rubbing roller. If a rubbed substrate is used for the preparation
of a retardation film according to the invention, the direction of the optical axis
of the film usually corresponds to the rubbing direction of the substrate.
[0063] Planar alignment with a low tilt angle can also be achieved or enhanced by adding
one or more surfactants to the polymerizable mesogenic material. Suitable surfactants
are described for example in J. Cognard, Mol.Cryst.Liq.Cryst.
78, Supplement 1, 1-77 (1981). Particularly preferred are non-ionic surfactants, e.g.
non-ionic fluorocarbon surfactants, like the commercially available Fluorad® (from
3M), or Zonyl FSO ® (from DuPont).
[0064] Reviews of further alignment techniques are given for example by I. Sage in "Thermotropic
Liquid Crystals", edited by G. W. Gray, John Wiley & Sons, 1987, pages 75-77, and
by T. Uchida and H. Seki in "Liquid Crystals - Applications and Uses Vol. 3", edited
by B. Bahadur, World Scientific Publishing, Singapore 1992, pages 1-63. A review of
alignment materials and techniques is given by J. Cognard, Mol. Cryst. Liq. Cryst.
78, Supplement 1 (1981), pages 1-77.
[0065] Polymerisation of the material takes place by exposing it to heat or actinic radiation.
Actinic radiation means irradiation with light, like UV light, IR light or visible
light, irradiation with X-rays or gamma rays or irradiation with high energy particles,
such as ions or electrons. Preferably polymerisation is carried out by UV irradiation.
As a source for actinic radiation for example a single UV lamp or a set of UV lamps
can be used. When using a high lamp power the curing time can be reduced. Another
possible source for actinic radiation is a laser, like e.g. a UV laser, an IR laser
or a visible laser.
[0066] The polymerisation is carried out in the presence of an initiator absorbing at the
wavelength of the actinic radiation. For example, when polymerising by means of UV
light, a photoinitiator can be used that decomposes under UV irradiation to produce
free radicals or ions that start the polymerisation reaction. When curing polymerisable
compounds with acrylate or methacrylate groups, preferably a radical photoinitiator
is used, when curing polymerisable compounds with vinyl and epoxide groups, preferably
a cationic photoinitiator is used. It is also possible to use a polymerisation initiator
that decomposes when heated to produce free radicals or ions that start the polymerisation.
As a photoinitiator for radical polymerisation for example the commercially available
Irgacure® or Darocure® initiators (from Ciba Geigy AG) can be used, whereas in case
of cationic photopolymerisation the commercially available UVI 6974® (Union Carbide)
can be used. The polymerisable material preferably comprises 0.01 to 10 %, very preferably
0.05 to 5 %, in particular 0.1 to 3 % of a polymerisation initiator. UV photoinitiators
are preferred, in particular radicalic UV photoinitiators.
[0067] The curing time is dependent, inter alia, on the reactivity of the polymerisable
material, the thickness of the printed layer, the type of polymerisation initiator
and the power of the UV lamp. The curing time according to the invention is preferably
not longer than 10 minutes, particularly preferably not longer than 5 minutes and
very particularly preferably shorter than 2 minutes. For mass production short curing
times of 3 minutes or less, very preferably of 1 minute or less, in particular of
30 seconds or less, are preferred.
[0068] The polymerisable liquid crystal material can additionally comprise one or more other
suitable components or additives such as, for example, catalysts, sensitizers, stabilizers,
inhibitors, co-reacting monomers, surface-active compounds, lubricating agents, wetting
agents, dispersing agents, hydrophobing agents, adhesive agents, flow improvers, defoaming
agents, deaerators, diluents, reactive diluents, auxiliaries, colourants, dyes or
pigments.
[0069] Suitable additives are disclosed for example in WO 00/47694, the entire disclosure
of which is incorporated into this application by reference.
[0070] In particular the addition of stabilizers is preferred in order to prevent undesired
spontaneous polymerisation of the polymerisable material for example during storage.
As stabilizers in principal all compounds can be used that are known to the skilled
in the art for this purpose. These compounds are commercially available in a broad
variety. Typical examples for stabilizers are 4-ethoxyphenol or butylated hydroxytoluene
(BHT).
[0071] Other additives, like e.g. chain transfer agents, can also be added to the polymerisable
liquid crystal material in order to modify the physical properties of the resulting
polymer film. When adding a chain transfer agent, such as monofunctional thiol compounds
like e.g. dodecane thiol or multifunctional thiol compounds like e.g. trimethylpropane
tri(3-mercaptopropionate), or a mesogenic or liquid crystalline thiol, to the polymerisable
material, the length of the free polymer chains and/or the length of the polymer chains
between two crosslinks in the inventive polymer film can be controlled. When the amount
of the chain transfer agent is increased, the polymer chain length in the obtained
polymer film is decreasing.
[0072] It is also possible, in order to increase crosslinking of the polymers, to add up
to 20% of a non mesogenic compound with two or more polymerisable groups to the polymerisable
liquid crystal material alternatively or in addition to the di- or multireactive polymerisable
mesogenic compounds to increase crosslinking of the polymer. Typical examples for
direactive non mesogenic monomers are alkyl diacrylates or alkyl dimethacrylates with
alkyl groups of 1 to 20 C atoms. Typical examples for non mesogenic monomers with
more than two polymerisable groups are trimethylpropane trimethacrylate or pentaerythritol
tetraacrylate.
[0073] In another preferred embodiment the polymerisable liquid crystal material comprises
up to 70%, preferably 3 to 50 % of a non mesogenic compound with one polymerisable
group. Typical examples for monoreactive non mesogenic monomers are alkyl acrylates
or alkyl methacrylates with alkyl groups of 1 to 20 C atoms.
[0074] It is also possible to add, for example, a quantity of up to 20% by weight of a non
polymerisable liquid crystal compound to adapt the optical properties of the resulting
polymer film.
[0075] The polymerisation is preferably carried out in the liquid crystal phase of the polymerisable
liquid crystal material. Therefore, preferably polymerisable mesogenic compounds or
mixtures with low melting points and broad liquid crystal phase ranges are used. The
use of such materials allows to reduce the polymerisation temperature, which makes
the polymerisation process easier and is a considerable advantage especially for mass
production. The selection of suitable polymerisation temperatures depends mainly on
the clearing point of the polymerisable material and inter alia on the softening point
of the substrate. Preferably the polymerisation temperature is at least 30 degrees
below the clearing temperature of the polymerisable mesogenic mixture. Polymerisation
temperatures below 120 °C are preferred. Especially preferred are temperatures below
90 °C, in particular temperatures of 60 °C or less.
[0076] The liquid crystal film obtained by the inventive process can be used in optical
elements, like reflective polarisers, retardation films, compensators, colour filters
or holographic elements, especially in films with patterned optical properties, for
the preparation of liquid crystal pigments, in decorative and security applications,
especially in security markings that are applied to items or documents of value for
easy identification or prevention of falsification, in nonlinear optics, optical recording
or information storage.
[0077] The liquid crystal film according to the present invention is especially useful as
security marking for authentification, identification, verification or prevention
of copying or counterfeiting of high value documents like ID cards, passports, bank
notes, credit cards, or any product with money value like stamps, tickets, shares,
cheques etc.. The film can be either included in a laminate or adhesively bound to
the surface of the document or as a transparent or watermark area.
[0078] The liquid crystal film can be used for direct application e.g. onto an article,
device or document, or as thread, hologram, transfer foil or hot stamping foil in
decorative or security applications as mentioned above or for the identification of
hidden images, informations or patterns. It can be applied to consumer products or
household objects, car bodies, foils, packing materials, clothes or woven fabric,
incorporated into plastic, or applied as security marking or thread on documents of
value.
[0079] In the foregoing and in the following examples, unless otherwise indicated, all temperatures
are set forth uncorrected in degrees Celsius and all parts and percentages are by
weight. Unless stated otherwise, the preferred amounts of mixture components as given
above and below relate to a solventless mixture.
Example 1
[0081] Compounds (A), (B) and (D) can be prepared according to or in analogy to the methods
described in D.J.Broer et al., Makromol.Chem.
190, 3201-3215 (1989). Compound (C) and its preparation are described in GB 2,280,445.
Irgacure 907 ® is a commercially available photoinitiator (Ciba Geigy). Iriodin LS800
® is a commercially available interference pigment (Merck KGaA).
[0082] The solution is coated onto a clear TAC substrate using a white K Bar with a wet
film thickness of ca. 4µm. The solvent is allowed to evaporate off at 50°C and the
coated film then laminated using another TAC laminate. Curing is achieved by irradiation
with UV radiation (Mercury vapour lamp). The cured, laminated product is then marked
by exposure to laser intensity light. The laser used was a Nd:YAG laser at 1064 nm
with a power of 100 W.
[0083] When viewed between crossed polarisers, or if the film is viewed through a single
linear polariser against a reflective background, the unmarked film shows distinct
birefringence colours as the polariser is roated. After laser irradiation the film
in the marked region shows as a uniform colour that does not change as the polariser
is rotated.