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WO2011069690A1 - Marquage modifié à base de polymères cristaux liquides chiraux - Google Patents

Marquage modifié à base de polymères cristaux liquides chiraux Download PDF

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Publication number
WO2011069690A1
WO2011069690A1 PCT/EP2010/056874 EP2010056874W WO2011069690A1 WO 2011069690 A1 WO2011069690 A1 WO 2011069690A1 EP 2010056874 W EP2010056874 W EP 2010056874W WO 2011069690 A1 WO2011069690 A1 WO 2011069690A1
Authority
WO
WIPO (PCT)
Prior art keywords
liquid crystal
marking
composition
chiral
chiral liquid
Prior art date
Application number
PCT/EP2010/056874
Other languages
English (en)
Inventor
Thomas Tiller
Frédéric Gremaud
Andrea Callegari
Olivier Rozumek
Brahim Kerkar
Original Assignee
Sicpa Holding Sa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to UAA201208214A priority Critical patent/UA104660C2/ru
Priority to BR112012013585A priority patent/BR112012013585A2/pt
Priority to JP2012542408A priority patent/JP5659430B2/ja
Priority to ES10722053.5T priority patent/ES2498725T3/es
Priority to EA201290454A priority patent/EA022293B1/ru
Priority to CA2781460A priority patent/CA2781460A1/fr
Priority to EP10722053.5A priority patent/EP2509792B1/fr
Priority to AU2010330332A priority patent/AU2010330332A1/en
Application filed by Sicpa Holding Sa filed Critical Sicpa Holding Sa
Priority to AP2012006326A priority patent/AP3477A/xx
Priority to MX2012006205A priority patent/MX2012006205A/es
Priority to CN201080055597.XA priority patent/CN102648097B/zh
Priority to UY33083A priority patent/UY33083A/es
Priority to SA110310900A priority patent/SA110310900B1/ar
Priority to ARP100104529A priority patent/AR080628A1/es
Priority to TW099142551A priority patent/TW201137092A/zh
Publication of WO2011069690A1 publication Critical patent/WO2011069690A1/fr
Priority to TNP2012000235A priority patent/TN2012000235A1/en
Priority to IL219905A priority patent/IL219905A0/en
Priority to MA34915A priority patent/MA33778B1/fr
Priority to ZA2012/04130A priority patent/ZA201204130B/en
Priority to HK12113194.3A priority patent/HK1172296A1/xx

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M3/00—Printing processes to produce particular kinds of printed work, e.g. patterns
    • B41M3/14—Security printing
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B42—BOOKBINDING; ALBUMS; FILES; SPECIAL PRINTED MATTER
    • B42D—BOOKS; BOOK COVERS; LOOSE LEAVES; PRINTED MATTER CHARACTERISED BY IDENTIFICATION OR SECURITY FEATURES; PRINTED MATTER OF SPECIAL FORMAT OR STYLE NOT OTHERWISE PROVIDED FOR; DEVICES FOR USE THEREWITH AND NOT OTHERWISE PROVIDED FOR; MOVABLE-STRIP WRITING OR READING APPARATUS
    • B42D25/00—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof
    • B42D25/30—Identification or security features, e.g. for preventing forgery
    • B42D25/36—Identification or security features, e.g. for preventing forgery comprising special materials
    • B42D25/364—Liquid crystals
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/28—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/28—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating
    • B41M5/281—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating using liquid crystals only
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B42—BOOKBINDING; ALBUMS; FILES; SPECIAL PRINTED MATTER
    • B42D—BOOKS; BOOK COVERS; LOOSE LEAVES; PRINTED MATTER CHARACTERISED BY IDENTIFICATION OR SECURITY FEATURES; PRINTED MATTER OF SPECIAL FORMAT OR STYLE NOT OTHERWISE PROVIDED FOR; DEVICES FOR USE THEREWITH AND NOT OTHERWISE PROVIDED FOR; MOVABLE-STRIP WRITING OR READING APPARATUS
    • B42D25/00—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof
    • B42D25/20—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof characterised by a particular use or purpose
    • B42D25/21—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof characterised by a particular use or purpose for multiple purposes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B42—BOOKBINDING; ALBUMS; FILES; SPECIAL PRINTED MATTER
    • B42D—BOOKS; BOOK COVERS; LOOSE LEAVES; PRINTED MATTER CHARACTERISED BY IDENTIFICATION OR SECURITY FEATURES; PRINTED MATTER OF SPECIAL FORMAT OR STYLE NOT OTHERWISE PROVIDED FOR; DEVICES FOR USE THEREWITH AND NOT OTHERWISE PROVIDED FOR; MOVABLE-STRIP WRITING OR READING APPARATUS
    • B42D25/00—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof
    • B42D25/20—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof characterised by a particular use or purpose
    • B42D25/23—Identity cards
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B42—BOOKBINDING; ALBUMS; FILES; SPECIAL PRINTED MATTER
    • B42D—BOOKS; BOOK COVERS; LOOSE LEAVES; PRINTED MATTER CHARACTERISED BY IDENTIFICATION OR SECURITY FEATURES; PRINTED MATTER OF SPECIAL FORMAT OR STYLE NOT OTHERWISE PROVIDED FOR; DEVICES FOR USE THEREWITH AND NOT OTHERWISE PROVIDED FOR; MOVABLE-STRIP WRITING OR READING APPARATUS
    • B42D25/00—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof
    • B42D25/20—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof characterised by a particular use or purpose
    • B42D25/24—Passports
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B42—BOOKBINDING; ALBUMS; FILES; SPECIAL PRINTED MATTER
    • B42D—BOOKS; BOOK COVERS; LOOSE LEAVES; PRINTED MATTER CHARACTERISED BY IDENTIFICATION OR SECURITY FEATURES; PRINTED MATTER OF SPECIAL FORMAT OR STYLE NOT OTHERWISE PROVIDED FOR; DEVICES FOR USE THEREWITH AND NOT OTHERWISE PROVIDED FOR; MOVABLE-STRIP WRITING OR READING APPARATUS
    • B42D25/00—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof
    • B42D25/20—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof characterised by a particular use or purpose
    • B42D25/29—Securities; Bank notes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B42—BOOKBINDING; ALBUMS; FILES; SPECIAL PRINTED MATTER
    • B42D—BOOKS; BOOK COVERS; LOOSE LEAVES; PRINTED MATTER CHARACTERISED BY IDENTIFICATION OR SECURITY FEATURES; PRINTED MATTER OF SPECIAL FORMAT OR STYLE NOT OTHERWISE PROVIDED FOR; DEVICES FOR USE THEREWITH AND NOT OTHERWISE PROVIDED FOR; MOVABLE-STRIP WRITING OR READING APPARATUS
    • B42D25/00—Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof
    • B42D25/40—Manufacture
    • B42D25/405—Marking
    • B42D25/415—Marking using chemicals
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
    • C09D11/037—Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/50—Sympathetic, colour changing or similar inks
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
    • C09K19/58—Dopants or charge transfer agents
    • C09K19/586—Optically active dopants; chiral dopants
    • C09K19/588—Heterocyclic compounds
    • B42D2033/20—
    • B42D2033/26—
    • B42D2035/20—
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K2019/0444—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group
    • C09K2019/0448—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group the end chain group being a polymerizable end group, e.g. -Sp-P or acrylate
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/06—Substrate layer characterised by chemical composition
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
    • Y10T428/24835—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including developable image or soluble portion in coating or impregnation [e.g., safety paper, etc.]

Definitions

  • the present invention relates to a marking based on chiral nematic (also called cholesteric) liquid crystal polymers.
  • the invention also relates to a method for the modification of chiral nematic liquid-crystal films, in which a chiral nematic liquid- crystal layer is locally or selectively (one or more region(s)) modified with the aid of a modifying composition.
  • counterfeit products or goods with counterfeit conformity assessment marks can also represent serious health and safety problems.
  • Such products may include adulterated or contaminated food, hazardous toys, falsified electrical goods and spare parts for cars.
  • the World Health Organization has identified counterfeit medicines as an enormous threat to health, potentially causing serious harm to patients and sometimes leading to death.
  • a classic way to protect products or goods from counterfeit is to mark them with a unique identifier.
  • the marking can be in the form of, for example, a code, indicia or a data matrix.
  • WO 2003/049047 the entire disclosure of which is incoiporated by reference herein, describes a method and apparatus for applying unique composite indicia or makings to a succession of articles, in which each unique composite indicium comprises two or more indicia. At least part of each of the indicia may be co-located at a predetermined location on the article with such co-location being unique or distinct for each composite indicium for each article.
  • the indicium may be overprinted with one or more images, logos or colour-schemes.
  • a code e.g. an alphanumeric code
  • a code that is stored in a database may be derived from the composite indicium from one or more mathematical properties. The code may be later accessed for identifying or verifying the article with indicium.
  • WO 2006/1 18889 the entire disclosure of which is incoiporated by reference herein, relates to an article including a chemiluminescent substance. This document further relates to methods and a device which detect the presence of chemiluminescence for purposes of communicating information associated with the article. Useful applications of the invention include confirmation of the authenticity of an article or its contents, or conversely forgery detection.
  • the method according to the invention relates to an information step providing visible indicia.
  • WO 2009/121605 discloses a marking of polymeric liquid crystal material having predetermined optical characteristics allowing its authentication and reading by a machine and its authentication by the human eye. The marking is applied onto an item, good or article. The marking is in the form of indicia representing a unique code which allows for an easy authentication by the human eye and a secure tracking and tracing of the marked item, good or article throughout is life cycle.
  • the present invention provides a liquid crystal polymer marking.
  • the marking is obtainable by a process which comprises:
  • the at least one modifying composition may at least partially convert the first chiral liquid crystal state into a (predominantly or substantially) isotropic state.
  • the at least one modifying composition may at least partially convert the first chiral liquid crystal state into a second chiral liquid crystal state that is different from the first state.
  • in stage (iii) at least two or at least three different modifying compositions are applied simultaneously or consecutively.
  • the chiral liquid crystal precursor composition may comprise (i) one or more (e.g.
  • both the one or more nematic compounds A and the one or more chiral dopant compounds B may comprise at least one compound which comprises at least one polymerizable group.
  • all of the one or more nematic compounds A and all of the one or more chiral dopant compounds B may comprise at least one polymerizable group.
  • the chiral liquid crystal precursor composition may comprise at least one chiral dopant compound B of formula (I):
  • Ri, R 2 , Rj, R4, R5, R ⁇ profession R7 and R 8 each independently denote C
  • A] and A 2 each independently denote a group of formula (i) to (iii):
  • D 2 denotes a group of formula
  • n, o, p, q, r, s, and t each independently denote 0, 1, or 2;
  • y denotes 0, 1 , 2, 3, 4, 5, or 6;
  • z 0 if y equals 0 and z equals 1 if y equals 1 to 6.
  • the at least one modifying composition may comprise at least one compound that is selected from ketones having from 3 to about 6 carbon atoms (e.g., 3, 4, 5 or 6 carbon atoms), alkyl esters and dialkylamides of carboxylic acids which comprise a total of from 2 to about 6 carbon atoms (e.g., 2, 3, 4, 5 or 6 carbon atoms), dialkyl sulfoxides comprising a total of from 2 to about 4 carbon atoms (e.g., 2, 3 or 4 carbon atoms), and optionally substituted nitrobenzene.
  • the at least one modifying agent may comprise at least one of dimethyl ketone, methyl ethyl ketone, ethyl acetate, dimethyl formamide, dimethyl sulfoxide, and nitrobenzene.
  • the at least one modifying composition may comprise a second chiral liquid crystal precursor composition.
  • the first chiral liquid crystal precursor composition and the second chiral liquid crystal precursor composition may be identical.
  • the first and second chiral liquid crystal precursor compositions may be different from each other.
  • the second chiral liquid crystal precursor composition may differ from the first chiral liquid crystal precursor composition at least in that the second composition comprises at least one of the one or more chiral dopant compounds B in a concentration which is different from a concentration of the same chiral dopant compound in the first composition and/or at least in that the second composition comprises at least one chiral dopant compound B which is different from any of the one of the one or more chiral dopant compounds B that are present in the first composition.
  • the at least one modifying composition may comprise a chiral dopant composition.
  • the chiral dopant composition may comprise, for example, at least one chiral dopant compound C which is a compound of formula (I) as set forth above.
  • the chiral dopant composition may further comprise at least one chiral dopant compound D which is different from a compound of formula (I).
  • the modifying composition may further comprise at least one resin and/or at least one salt and/or at least one pigment and/or dye that absorbs in the visible or invisible region of the electromagnetic spectnam and/or at least one luminescent pigment and/or dye.
  • stage (ii) of the process may comprise a heating of the applied composition to a temperature of from about 55°C to about 150°C, e.g., from about 55°C to about 100°C, or from about 60°C to about 100°C.
  • stage (iii) of the process may comprise an application (e.g., deposition) of the at least one modifying composition by continuous ink-jet printing and/or drop-on-demand ink-jet printing and/or spray coating and/or valve-jet printing.
  • a stream of air may be passed over the surface of the one or more areas, preferably (substantially) parallel thereto.
  • the marking of the present invention may be in the form of at least one of an image, a picture, a logo, indicia, or a pattern representing a code selected from one or more of 1 -dimensional barcodes, stacked 1 -dimensional barcodes, 2- dimensional barcodes, 3 -dimensional barcodes, and a data matrix.
  • the present invention also provides a substrate which comprises (e.g., carries on a surface thereof) the marking of the present invention as set forth above, including the various aspects thereof.
  • the marking may serve as at least one of a security element, an authenticity element, an identification element, and a tracking and tracing element.
  • the substrate may be, or comprise, at least one of an identity document, a label, packaging, a banknote, a security document, a passport, a stamp, an ink-transfer film, and a reflective film.
  • the present invention also provides a security ink that comprises (i) one or more nematic compounds A and (ii) one or more chiral dopant compounds B which are capable of giving rise to a chol est eric state of the security ink upon application of heat thereto.
  • the security ink may comprise at least one chiral dopant compound B of formula (I) as set forth above.
  • the present invention also provides a method of providing a substrate with a liquid crystal polymer marking.
  • the method comprises: (i) applying a first chiral liquid crystal precursor composition onto at least one surface of a (solid) substrate;
  • the present invention also provides a substrate which comprises a marking (e.g., on at least one (outer) surface thereof).
  • the marking comprises a layer or film of a chiral liquid crystal polymer.
  • the layer or film comprises in at least one area (region) thereof a liquid crystal polymer that has at least one optical property which is different from an optical property of the remainder of the layer or film.
  • the liquid crystal polymer in the at least one area of the layer or film may comprise (e.g. may be in) an isotropic state. In another aspect, the liquid crystal polymer in the at least one area of the layer or film may comprise (e.g., may be in) an isotropic state.
  • the present invention also provides a substrate which comprises a marking (e.g., on at least one (outer) surface thereof).
  • the marking comprises a layer or film of a first chiral liquid ciystal polymer that has a first optical property.
  • the layer or film comprises in at least one area (region) thereof a second liquid crystal polymer that has at least one second optical property which is different from the first optical property.
  • the present invention also provides a substrate which comprises a marking (e.g., on at least one (outer) surface thereof).
  • the marking comprises a layer or film of a chiral liquid crystal polymer in a first chiral liquid crystal state.
  • the layer or film comprises in at least one area (region) thereof a liquid crystal polymer in a second chiral liquid crystal state that has at least one optical property which is different from an optical property of the polymer in the first chiral liquid crystal state.
  • Fig. 1 is a schematic drawing which illustrates nematic, smectic and cholesteric liquid crystals
  • Fig. 2 shows photographs of markings in accordance with the present invention.
  • the substrate for use in the present invention is not particularly limited and can be of various types.
  • the substrate may, for example, consist (essentially) of or comprise one or more of a metal (for example, in the form of a container such as a can for holding various items such as, e.g., beverages or foodstuffs), optical fibers, a woven, a coating, and equivalents thereof, a plastic material, glass (for example, in the form of a container such as a bottle for holding various items such as, e.g., beverages or foodstuffs), cardboard, packaging, paper, and a polymeric material.
  • a metal for example, in the form of a container such as a can for holding various items such as, e.g., beverages or foodstuffs
  • a plastic material, glass for example, in the form of a container such as a bottle for holding various items such as, e.g., beverages or foodstuffs
  • cardboard packaging, paper, and a polymeric material.
  • the substrate will preferably have
  • the substrate further will advantageously have a dark or black surface or background onto which the precursor composition is to be applied.
  • a dark or black background the light transmitted by the cholesteric liquid crystal material is largely absorbed by the background, whereby any residual backscattering from the background does not disturb the perception of the cholesteric liquid crystal material's own reflection with the unaided eye.
  • the reflection color of the cholesteric liquid crystal material is less visible when compared with a black or dark background, due to the strong backscattering from the background.
  • a cholesteric liquid crystal material can always be identified with the help of a circular polarization filter because it selectively reflects only one of the two possible circular polarized light components, in accordance with its chiral helical structure.
  • Non-limiting examples of suitable substrates include: cardboard darkened with black gravure ink (no overprinted varnish); cardboard darkened with black offset ink (no oveiprinted varnish); cardboard darkened with any black ink and overprinted with water based varnish; cardboard darkened with any black ink and oveiprinted with solvent varnish; metal treated with black coating.
  • any (preferably non-porous and preferably black) substrate (which may not necessarily be flat and may be uneven) whose coating is not soluble, or only slightly soluble, in the solvent(s) used in the chiral liquid precursor composition and in the modifying agent is a suitable substrate for the purposes of the present invention.
  • the chiral liquid crystal precursor composition that is used for making the marking according to the present invention and is applied (e.g., deposited) onto at least a part of at least one surface of the substrate comprises a mixture of (i) one or more nematic compounds A and (ii) one or more cholesteric (i.e., chiral dopant) compounds B (including cholesterol) which are capable of giving rise to a cholesteric state of the composition.
  • the pitch of the obtainable cholesteric state depends on the relative ratio of the nematic and the cholesteric compounds.
  • the (total) concentration of the one or more nematic compounds A in the chiral liquid crystal precursor composition for use in the present invention will be about five to about twenty times the (total) concentration of the one or more cholesteric compounds B,
  • a precursor composition with a high concentration of cholesteric compounds is not desirable (although possible in many cases) because the one or more cholesteric compounds tend to crystallize, thereby making it impossible to obtain the desired liquid crystal state having specific optical properties.
  • Nematic compounds A which are suitable for use in the chiral liquid crystal precursor composition are known in the art; when used alone (i.e., without cholesteric compounds) they arrange themselves in a state characterized by its birefringence.
  • Non- limiting examples of nematic compounds A which are suitable for use in the present invention are described in, e.g., WO 93/22397, WO 95/22586, EP-B-0 847 432, U.S. Patent No. 6,589,445, US 2007/0224341 Al and JP 2009-300662 A. The entire disclosures of these documents are incorporated by reference herein.
  • a preferred class of nematic compounds for use in the present invention comprises one or more (e.g., 1, 2 or 3) polymerizable groups, identical or different from each other, per molecule.
  • polymerizable groups include groups which are capable of taking part in a free radical polymerization and in particular, groups comprising a carbon-carbon double or triple bond such as, e.g., an acrylate moiety, a vinyl moiety or an acetylenic moiety.
  • Particularly preferred as polymerizable groups are acrylate moieties.
  • the nematic compounds for use in the present invention further may comprise one or more (e.g., 1 , 2, 3, 4, 5 or 6) optionally substituted aromatic groups, preferably phenyl groups.
  • Examples of the optional substiruents of the aromatic groups include those which are set forth herein as examples of substituent groups on the phenyl rings of the chiral dopant compounds of formula (I) such as, e.g., alkyl and alkoxy groups.
  • Examples of groups which may optionally be present to link the polymerizable groups and the aryl (e.g., phenyl) groups in the nematic compounds A include those which are exemplified herein for the chiral dopant compounds B of fonnula (I) (including those of formula (IA) and formula (IB) set forth below).
  • the nematic compounds A may comprise one or more groups of formula (i) to (iii) which are indicated above as meanings for A] and A 2 in formula (I) (and formulae (IA) and (IB)), typically bonded to optionally substituted phenyl groups.
  • Specific non-limiting examples of nematic compounds which are suitable for use in the present invention are given below in the Example.
  • the one or more nematic compounds A (and also the one or more chiral dopant compounds B) for use in the present invention to be substantially free of compounds which do not comprise any polymerizable group (i.e., to preferably comprise compounds without any polymerizable group merely as impurities, if at all). It also is preferred for the nematic compounds to be different from cellulose derivatives.
  • the one or more cholesteric (i.e., chiral dopant) compounds B for use in the chiral liquid crystal precursor composition (and also one or more chiral dopant compounds in a chiral dopant composition used as modifying composition) preferably comprise at least one polymerizable group.
  • suitable examples of the one or more chiral dopant compounds B include those of formula (I):
  • R[, R 2 , R3, 4, R5, R f i, R7 and R 8 each independently denote C C 6 alkyl and C] -C 6 alkoxy;
  • Ai and A 2 each independently denote a group of formula (i) to (iii):
  • D 1 denotes a group of formula
  • n 1 , or 2;
  • y denotes 0, 1 , 2, 3, 4, 5, or 6;
  • the one or more chiral dopant compounds B may comprise one or more isomannide derivatives of formula (IA):
  • R] R 2 R 3 , R4, R 5 , R f o R 7 and R 8 each independently denote Ci-C 6 alkyl and C[-C 6 alkoxy;
  • A, and A 2 each independently denote a group of formula (i) to (iii):
  • Dj denotes a group of formula
  • D 2 denotes a group of formula
  • (Re), m, n, o, p, q, r, s, and t each independently denote 0, 1 , or 2; y denotes 0, 1 , 2, 3, 4, 5, or 6; z equals 0 if y equals 0 and z equals 1 if y equals 1 to 6.
  • Rj, R 2 , R 3 , R , R5, Re, 7 and Rs each independently denote Ci-Q, alkyl.
  • Ri, R 2 , R3, R4, R5, Re, R7 and R 3 ⁇ 4 in formula (IA) (and in formula (I)) each independently denote Ci-C 6 alkoxy.
  • the one or more chiral dopant compounds B may comprise one or more isosorbide derivatives represented by formula (IB):
  • Ri, R 2 , R3, 4, R5, e, R7 and R s each independently denote C,-C 6 alkyl and Ci-Q, alkoxy;
  • Ai and A 2 each independently denote a group of formula (i) to (iii):
  • D 1 denotes a group of formula
  • D 2 denotes a group of formula
  • m, n, o, p, q, r, s, and t each independently denote 0, 1, or 2; y denotes 0, 1 , 2, 3, 4, 5, or 6; z equals 0 if y equals 0 and z equals 1 if y equals 1 to 6.
  • . R 2 , R 3 , R4, R 5 , R 6 , R 7 and Rg each independently denote C] -C 6 alkyl.
  • R s , R 2 , R 3 , R4, R5, R3 ⁇ 4, R 7 and Rg in formula (IB) each independently denote Ci-Cg alkoxy.
  • R t , R 2 , R 3 and R4 each independently denote C ⁇ -C alkyl; and
  • m, n, o, and p each independently denote 0, 1 , or 2.
  • Rj , R 2 , R 3 and R4 each independently denote Ci-Ce alkoxy; and
  • m, n, o, and p each independently denote 0, 1 , or 2.
  • the alkyl and alkoxy groups of R) , R 2 , R 3 , R4, R5, R 6 , R 7 and Rg in formulae (I), (I A) and (IB) may comprise 3, 4, 6 or 7 carbon atoms and in particular, 4 or 6 carbon atoms.
  • alkyl groups comprising 3 or 4 carbon atoms include isopropyl and butyl.
  • alkyl groups comprising 6 or 7 carbon atoms include hexyl, 2- methylpentyl, 3-methylpentyl, 2,2-dimethylpentyl, and 2,3-dimethylpentyl.
  • alkoxy groups comprising 3 or 4 carbon atoms include isopropoxy, but-l -oxy, but-2-oxy, and teri-butoxy.
  • alkoxy groups comprising 6 or 7 carbon atoms include hex-l -oxy, hex-2-oxy, hex-3-oxy, 2-methylpent-l -oxy, 2- methylpent-2-oxy, 2-methylpent-3-oxy, 2-methylpent-4-oxy, 4-methylpent-l-oxy, 3- methylpent-l -oxy, 3-methylpent-2-oxy, 3-methylpent-3-oxy, 2,2-dimethylpent-l-oxy, 2,2-dimethylpent-3-oxy, 2,2-dimethylpent-4-oxy, 4,4-dimethyIpent-l -oxy, 2,3- dimethylpent-l-oxy, 2,3-dimethylpent-2-oxy, 2,3-dimefhylpent-3-oxy, 2,3-dimethylpent- 4-oxy, and 3,4-dimethylpent-l-oxy.
  • Non-limiting specific examples of chiral dopant compounds B of formula (1) for use in the present invention are provided in the Example below.
  • the one or more chiral dopant compounds B will usually be present in the precursor composition in a total concentration of from about 0.1% to about 30% by weight, e.g., from about 0.1% to about 25%, or from about 0.1 %) to about 20% by weight, based on the total weight of the composition.
  • the one or more nematic compounds A will often be present in a concentration of from about 30% to about 50% by weight, based on the total weight of the precursor composition.
  • the application (e.g., deposition) of the precursor composition is preferably carried out with a printing technique, and in particular, a printing technique selected from at least one of continuous ink-jet printing, drop -on-demand ink-jet printing, and spray coating.
  • a printing technique selected from at least one of continuous ink-jet printing, drop -on-demand ink-jet printing, and spray coating.
  • ink-jet printing is employed.
  • the industrial ink-jet printers, commonly used for numbering, coding and marking applications on conditioning lines and printing presses, are particularly suitable.
  • Preferred ink-jet printers include single nozzle continuous ink-jet printers (also called raster or multi level deflected printers) and drop- on-demand ink-jet printers, in particular valve-jet printers.
  • the thickness of the applied precursor composition will usually be from about 3 to about 20 ⁇ , e.g., from about 5 to about 15 ⁇ .
  • the precursor composition will usually comprise a solvent to adjust its viscosity to a value which is suitable for the employed application (printing) teclinique.
  • Typical viscosity values for ink-jet printing inks are in the range of from about 4 to about 30 mPa.s at 25°C. Suitable solvents are known to those of skill in the art.
  • Non-limiting examples thereof include low-viscosity, slightly polar and aprotic organic solvents, such as, e.g., methyl ethyl ketone (MEK), acetone, ethyl acetate, ethyl 3-ethoxypropionate, toluene and mixtures of two or more thereof.
  • MEK methyl ethyl ketone
  • the precursor composition for use in the present invention will usually also comprise at least one conductivity agent (for example, a salt).
  • the conductivity agent will have a non-negligible solubility in the composition.
  • Non-limiting examples of suitable conductivity agents include salts such as, e.g., tetraalkyl ammonium salts (e.g., tetrabutyl ammonium nitrate, tetrabutyl ammonium perchlorate and tetrabutyl ammonium hexafluorophosphate), alkali metal thiocyanates such as potassium thiocyanate and alkali metal perchlorates such as lithium perchlorate.
  • the conductivity agent will be present in a concentration which is sufficient to provide the conductivity which is required or desirable. Of course, mixtures of two or more different conductivity agents (salts) can be used.
  • the composition for use in the present invention is to be cured/polymerized by UV radiation the composition will also comprise at least one photoinitiator that shows a non-negligible solubility in the composition.
  • photoinitiators include a-hydroxyketones such as 1 - hydroxy-cyclohexyl -phenyl-ketone and a mixture (e.g., about 1 : 1) of 1-hydroxy- cyclohexyi-phenyl -ketone and one or more of benzophenone, 2-hydroxy-2-methyl ⁇ l- phenyl-l -propanone, and 2 -hydroxy- 1 -[4-(2-hydroxyetlioxy)phenyl]-2-methyl-l- propanone; phenylglyoxylates such as methylbenzoylformate and a mixture of oxy- phenyl-acetic acid 2-[2-oxo-2-phenyl-acetoxy
  • the precursor composition is to be cured by a method which is different from irradiation with UV light such as, e.g., by means of high-energy particles (e.g., electron beams), X-rays, gamma-rays, etc.
  • a photoinitiator can, of course, be dispensed with.
  • the chiral liquid crystal precursor composition for use in the present invention may also comprise a variety of other optional components which are suitable and/or desirable for achieving a particular desired property of the composition and in general, may comprise any components/substances which do not adversely affect a required property of the precursor composition to any significant extent.
  • optional components are resins, silane compounds, sensitizers for the photoinitators (if present), etc.
  • the composition may comprise one or more silane compounds which show a non-negligible solubility in the composition.
  • Non-limiting examples of suitable silane compounds include optionally polymerizable silanes such as those of formula R1R2R3-S1-R4 wherein R ] > R 2 , and R 3 independently represent alkoxy and alkoxyalkoxy having a total of from 1 to about 6 carbon atoms and R 4 represents vinyl, allyl, (C M o)alkyl, (meth)acryloxy(Cj_6)alkyl, and glycidyloxy(C i .
  • optionally polymerizable silanes such as those of formula R1R2R3-S1-R4 wherein R ] > R 2 , and R 3 independently represent alkoxy and alkoxyalkoxy having a total of from 1 to about 6 carbon atoms and R 4 represents vinyl, allyl, (C M o)alkyl, (meth)acryloxy(Cj_6)alkyl, and glycidyloxy(C i .
  • the concentration of the one or more silane compounds, if present, in the precursor composition will usually be from about 0.5% to about 5% by weight, based on the total weight of the composition.
  • the precursor composition is brought to a first chiral liquid crystal state having specific optical properties.
  • the chiral liquid crystal precursor composition is heated, the solvent contained in the composition, if present, is evaporated and the promotion of the desired chiral liquid crystal state takes place.
  • the temperature used to evaporate the solvent and to promote the formation of the liquid crystal state depends on the components of the chiral liquid crystal precursor composition and will in many cases range from about 55°C to about 150°C, e.g., from about 55°C to about 100°C, preferably from about 60°C to about 100°C.
  • suitable heating sources include conventional heating means and in particular, radiation sources such as, e.g., an IR lamp.
  • the required heating time depends on several factors such as, e.g., the components of the precursor composition, the type of heating device and the intensity of the heating (energy output of the heating device). In many cases a heating time of from about 1 second to about 30 seconds such as, e.g., not more than about 20 seconds, not more than about 10 seconds, or not more than about 5 seconds will be sufficient.
  • the term "specific optical properties" is to be understood as a liquid crystal state with a specific pitch that reflects a specific wavelength range.
  • An advantage of the precursor composition which contains a chiral dopant compound according to formula (1) and related formulae is the ability to generate a stable liquid crystal state quickly after the heating (and evaporation of the solvent).
  • the liquid crystal states which are obtained after heating and evaporation of the solvent with precursor compositions of the prior art see, e.g., EP 1 299 375, EP 1 669 431 , and EP 1 339 812, the entire disclosures of which are incorporated by reference herein) very often can easily be disrupted by minor temperature changes.
  • a (at least one) modifying composition is applied onto one or more regions of the applied composition in the first chiral liquid crystal state.
  • the modifying composition is capable of changing the first chiral liquid crystal state (optionally upon heating, depending on the type of modifying composition).
  • the modifying composition may be applied while the chiral liquid crystal precursor composition is still in a heated state (e.g., immediately following the completion of the heating operation) or may be applied after the chiral liquid crystal precursor composition has cooled down to at least some extent (e.g., is at substantially room temperature).
  • the cooling of the precursor composition can be accelerated by means known to those of skill in the art such as, e.g., by blowing ambient air onto the previously heated composition.
  • Applying the modifying composition to the precursor composition in a cooled-down state may improve the resolution of the marking.
  • applying the modifying composition immediately after completion of the heating operation may be desirable if the entire process of making the marking is to be conducted in an as simple and speedy as possible manner.
  • the modifying composition for use in the present invention will not extract any of the compounds which form the chiral liquid crystal state and will also not modify the chemical stmcture of these compounds to any significant extent (and preferably, not at all). Without wishing to be bound by any theory, it is speculated that the modifying composition will initiate a very localized and controlled reorganization of the liquid crystal state. In this regard, it should be noted that the method of the present invention is fast and easy to implement industrially, and does not require complex means.
  • the modifying composition depending on its nature will usually modify the first chiral liquid crystal state from a (predominantly or substantially) anisotropic state which is characterized by specific optical properties to:
  • the modifying composition may, for example, be or comprise a modifying agent.
  • the modifying agent will usually comprise one or more aprotic organic compounds which are liquid at room temperature and preferably have a relatively high dipole moment and a relatively high dielectric constant.
  • Non-limiting examples thereof include ketones having from 3 to about 6 carbon atoms, alkyl esters and dialkylamides of carboxylic acids which comprise a total of from 2 to about 6 carbon atoms, dialkyl sulfoxides comprising a total of from 2 to about 4 carbon atoms, and optionally substituted (e.g., alkyl-substituted) nitrobenzene such as, e.g., dimethyl ketone, methyl ethyl ketone, ethyl acetate, dimethyl formamide, dimethyl sulfoxide, nitrobenzene, nitrotoluene, and mixtures of two or more thereof.
  • PrefeiTed compounds for use in the modifying agent include acetone, methyl ethyl ketone and ethyl acetate.
  • a modifying agent for use in the present invention may further comprise one or more resins to adjust its viscosity.
  • the resin(s) must be compatible with the application (e.g., printing) technique that is to be employed.
  • Non-limiting examples of resins which may be suitable, depending on the particular circumstances, include polyesters resins such as, e.g, DYNAPOL® L 1203 , L 205, L 206, L 208, L 210, L 41 1, L 651 , L658, L 850, L 912, L 952, LH 530, LH 538, LH 727, LH 744, LH 773, LH 775, LH 818, LH 820, LH 822, LH 912, LH 952, LH 530, LH 538, LH 727, LH 744, LH 773, LH 775, LH 818, LH 820, LH 822, LH 823, LH 826, LH 828, LH
  • the one or more resins are selected from DYNAPOL® L 1203 , L 205, L 206, L 208, L 210, L 41 1 , L 651 , L658, L 850, L 912, L 952, LH 530, LH 538, LH 727, LH 744 from Evonik.
  • a typical concentration range for the one or more resins is from about 3% to about 15% by weight, based on the total weight of the modifying agent.
  • the modifying agent may further comprise one or more conductivity agents such as, e.g., salts which are to impart sufficient conductivity to the modifying agent so as to allow its use in combination with a printer such as, e.g., a continuous ink-jet printer.
  • suitable conductivity agents include those which are set forth above as examples of conductivity agents for use in the precursor composition of the present invention such as, e.g., tetrabutyl ammonium nitrate, tetrabutyl ammonium perchlorate, tetrabutyl ammonium hexafiuorophosphate, potassium thiocyanate, lithium perchlorate and other conductivity agents known in the art.
  • the modifying agent comprises a solvent or a solvent mixture
  • the first chiral liquid crystal state will locally (in one or more region(s)) switch from a (predominantly or substantially) anisotropic state to a (predominantly or substantially) isotropic state.
  • the modifying composition may be or comprise a second chiral liquid crystal precursor composition.
  • the second chiral liquid crystal precursor composition which is applied in one or more areas on the first chiral liquid precursor composition in the first chiral liquid crystal state may be the same as or different from the first chiral liquid crystal precursor composition.
  • everything that is set forth above with respect to the first chiral liquid precursor composition e.g., components, application methods, etc. applies equally and without exception also to the second chiral liquid precursor composition.
  • the one or more chiral dopant compounds B will usually be present in the second chiral liquid crystal precursor composition in a total concentration of from about 0.1 % to about 30% by weight, e.g., from about 0.1 % to about 25%, or from about 0.1% to about 20% by weight, based on the total weight of the second composition.
  • the one or more nematic compounds A will often be present in the second chiral liquid crystal precursor composition in a concentration of from about 30% to about 50% by weight, based on the total weight of the second precursor composition.
  • the one or more differences may relate to, e.g., one or more of the compounds A and B that are present in these compositions and/or to the concentrations of one or more of these compounds.
  • a or the only difference between these compositions may be that one or more (or all) of the chiral dopant compounds B are present in the second composition in a concentration/concentrations that is/are different from the corresponding concentration/concentrations in the first composition.
  • first and second compositions may be that the one or more chiral dopant compounds B in the first composition are of formula (I) above and/or related formulae and at least one of the one or more chiral dopant compounds B in the second composition is different from formula (I) and/or related formulae.
  • at least one of the one or more chiral dopant compounds B in the second composition may be an isosorbide or isomannide derivative as described in, e.g., EP-B-0 847 432, GB-A-2 330 139, and U.S. Patent No. 6,589,445, the entire disclosures of which are incorporated by reference herein.
  • the second precursor composition After the application (e.g. deposition) of the second chiral liquid crystal precursor composition to one or more areas of the first chiral liquid crystal precursor composition in the first chiral liquid crystal state having first specific optical properties, the second precursor composition is brought to a second chiral liquid crystal state having second specific optical properties.
  • the solvent contained in the composition if present, is evaporated and the promotion of the desired second chiral liquid crystal state takes place.
  • the temperature used to evaporate the solvent and to promote the formation of the second liquid crystal state depends on the components of the second chiral liquid crystal precursor composition and will in many cases range from about 55°C to about 150°C, e.g., from about 55°C to about 100°C, preferably from about 60°C to about 100°C.
  • suitable heating sources include conventional heating means and in particular, radiation sources such as, e.g., an IR lamp.
  • the marking according to the present invention is not identical or comparable to a simple supeiposition of two chiral nematic liquid crystal layers. This constitutes a significant difference and a great advantage over the existing prior art.
  • first chiral liquid crystal precursor composition is deposited on a substrate and brought to the first chiral liquid crystal state this state is characterized by a pitch pi .
  • second chiral liquid crystal precursor composition is deposited on one or more areas of the applied first composition and brought to the second chiral liquid crystal state the second state is characterized by a pitch p2 (which may be the same or different from pi ).
  • the product that is obtained after stage (iv) and further cured/polymerized in stage (v) of the process of the present invention is not a supeiposition of a first chiral liquid crystal state having a pitch i and a second chiral liquid crystal state having a pitch p2. Rather, an area carrying the second chiral liquid crystal precursor composition, once brought to the second chiral liquid crystal state, has a pitch p2 ! which is different from pi and p2 but it is somewhat dependent on the nature of pi . Without wishing to be bound by any theory it is speculated that the first chiral liquid crystal state has an impact on the formation of the second chiral liquid crystal state.
  • the induction of the first chiral liquid crystal state on the second chiral liquid crystal precursor composition will accelerate and promote a second chiral liquid crystal state which is different from the chiral liquid crystal state that would be expected based solely on the second chiral liquid ciystal precursor composition alone.
  • the marking according to the present invention is controlled by the first chiral liquid crystal precursor composition which is only known by the producer of the marking. From different first chiral liquid crystal precursor compositions a large number of specific markings and codings can be generated and stored in a specific database which contains all of the markings or codings produced. Without wishing to be bound by any theory it is speculated that the second precursor composition will initiate a very local and controlled reorganization of the first chiral liquid crystal state. It further is to be noted that the method of the present invention is fast and easy to implement industrially, and does not require complex means.
  • the modifying composition may be or comprise a chiral dopant composition.
  • the chiral dopant composition preferably comprises one or more (e.g., one, two, three or four) chiral dopant compounds C of formula (I) set forth above and/or related formulae.
  • the chiral dopant composition comprises at least one chiral dopant compound C and at least one other chiral dopant D which is different from a compound of formula (I) and related formulae.
  • the at least one chiral dopant compound D may be selected, for example, from the derivatives of isosorbides and isomannides which are disclosed in, e.g., EP-B-0 847 432, GB-A-2 330 139, and U.S. Patent No. 6,589,445, the entire disclosures of which are incorporated by reference herein.
  • chiral dopant compounds C which are preferably present in the chiral dopant composition
  • the chiral dopant compounds B set forth above may, for example, be used. Accordingly, everything that is set forth above with respect to compounds B applies equally and without exception also to compounds C. Also, it is to be appreciated that a (or the only) chiral dopant compound C that is present in the chiral dopant composition may be identical to a (or the only) chiral dopant compound B that is present in the chiral liquid crystal precursor composition.
  • the chiral dopant composition will usually comprise the one or more chiral dopant compounds in a total concentration of from about 0.1 % to about 30% by weight, e.g., from about 0.1 % to about 25%, or from about 0.1 % to about 20% by weight, based on the total weight of the composition. Often, the total concentration will be from 3% to 10% by weight, e.g., from 5% to 8% by weight, based on the total weight of the precursor composition.
  • the composition will usually comprise a solvent to adjust its viscosity to a value which is suitable for the employed application (printing) technique.
  • Typical viscosity values for ink-jet printing inks are in the range of from about 4 to about 30 mPa.s at 25°C. Suitable solvents are known to those of skill in the art.
  • Non-limiting examples thereof include low-viscosity, slightly polar and aprotic organic solvents, such as, e.g., methyl ethyl ketone (MEK), acetone, ethyl acetate, ethyl 3-ethoxypropionate, toluene and mixtures of two or more thereof.
  • MEK methyl ethyl ketone
  • Others suitable components needed for printing techniques used in the context of the present invention may also be present (resins, salts, etc.) and are known to those of skilled in the art.
  • the chiral dopant composition may comprise one or more conductivity agents such as, e.g., salts which are to impart sufficient conductivity to the chiral dopant composition so as to allow its use in combination with a printer such as, e.g., a continuous ink-jet printer.
  • suitable conductivity agents include those which are set forth above as examples of conductivity agents for use in the precursor composition of the present invention such as, e.g., tetrabutyl ammonium nitrate, tetrabutyl ammonium perchlorate, tetrabutyl ammonium hexafluorophosphate, potassium thiocyanate, lithium perchlorate and other conductivity agents known in the art,
  • the chiral dopant composition After the application of the chiral dopant composition to one or more areas of the chiral liquid crystal precursor composition in the first chiral liquid crystal state having first specific optical properties, at least one of the one or more areas is brought to a second chiral liquid crystal state having second specific optical properties. To that end at least a part of the one or more areas onto which the chiral dopant composition has been applied is heated, the solvent contained in the composition, if present, is evaporated and the promotion of the desired second chiral liquid crystal state takes place.
  • the temperature used to evaporate the solvent and to promote the formation of the second liquid crystal state depends on, e.g., the components of chiral dopant composition and will in many cases range from about 55°C to about 150°C, e.g., from about 55°C to about 100°C, preferably from about 60°C to about 100°C.
  • suitable heating sources include conventional heating means and in particular, radiation sources such as, e.g., an IR lamp.
  • the deposition of the modifying composition is performed onto one or more regions of the chiral liquid crystal precursor composition in the first liquid crystal state preferably with a printing technique and in particular, a technique selected from continuous ink-jet printing, drop- on-demand ink-jet printing, valve-jet printing and spray coating.
  • a printing technique in particular, a technique selected from continuous ink-jet printing, drop- on-demand ink-jet printing, valve-jet printing and spray coating.
  • ink-jet techniques are used for applying the modifying composition.
  • the industrial ink-jet printers commonly used for numbering and coding and marking applications on conditioning lines and printing presses, are particularly suitable.
  • Preferred ink-jet printers are single nozzle continuous ink-jet printers (also called raster or multi level deflected printers) and drop-on-demand ink-jet printers, in particular valve-jet printers.
  • a stream of air is passed over the surface of the precursor composition, preferably (substantially) parallel thereto.
  • the stream of air can be generated by any means, e.g., with an industrial hair dryer.
  • the stream of air will preferably not be intense and/or of high speed.
  • the temperature of the air will usually be ambient (e.g., about 20°C) but may also be somewhat lower or higher, e.g., up to about 60°C, up to about 40°C, or up to about 30°C.
  • the phrase "immediately after the application of the modifying composition" is intended to mean without delay, e.g., within a period of not more than about 10 seconds, for example, not more than about 5 seconds, not more than about 3 seconds, not more than about 2 seconds, or not more than about 1 second following the completion of the application of the modifying composition.
  • the area of the applied (first) precursor composition onto which the modifying composition is applied will usually be from about 0.1 % to about 99.9% of the total area of the applied precursor composition.
  • the area will often be at least about 1 %, e.g., at least about 5% or at least about 10% and not higher than about 99%, e.g., not higher than about 95% or not higher than about 90% of the total area of the applied precursor composition.
  • the marking according to the present invention may be in the form of an image, a picture, a logo, indicia, and/or a pattern representing a ( D, 2D, 3D) code such as, e.g., a 1 -dimensional barcode, a stacked 1 -dimensional barcode, a 2 -dimensional barcode, a 3 ⁇ dimensional barcode and/or a data matrix.
  • a corresponding dimensional barcode e.g., a 1 -dimensional barcode, a stacked 1 -dimensional barcode, a 2 -dimensional barcode, a 3 ⁇ dimensional barcode and/or a data matrix.
  • the different modifying compositions may comprise two different chiral dopant compositions, or they may comprise a chiral dopant composition and a modifying agent and a second chiral liquid crystal precursor composition, or they may comprise two different second chiral liquid crystal precursor compositions and a modifying agent, or they may comprise a (at least one) modifying agent, a (at least one) second chiral liquid crystal precursor composition, and a (at least one) chiral dopant composition, etc.
  • first modifying composition and to thereafter apply a different second modifying composition in at least a part of the region(s) in which the initially applied first modifying composition has been applied (and, optionally, also in one or more regions where the first modifying composition has not been applied).
  • stage (iv) which is not required for a modifying composition which modifies the first chiral liquid crystal state locally in the one or more areas such as the modifying agent
  • stage (iv) which is not required for a modifying composition which modifies the first chiral liquid crystal state locally in the one or more areas such as the modifying agent
  • the precursor composition after the application of the modifying agent (and optionally, the passing of air over the surface of the precursor composition) to further modify the chiral liquid crystal state and/or to remove any residual solvent that was present in the modifying agent.
  • an (additional) heating operation after the application of the modifying agent does not result in any significant additional advantages.
  • the temperature used for this (optional) heating operation will in many cases range from about 55°C to about 150°C, e.g., from about 55°C to about 100°C, or from about 60°C to about 100°C.
  • suitable heating sources include conventional heating means and in particular, radiation sources such as, e.g., an IR lamp.
  • the printing process can be carried out with a multi-head system (with, e.g., two, three, four, five or more heads) wherein each head contains a different modifying composition.
  • a multi-head system with, e.g., two, three, four, five or more heads
  • each head contains a different modifying composition.
  • An advantage of such a configuration is that during the printing process one can obtain a sequentially different modification of the first liquid crystal state and therefore a great number of unique markings.
  • the multi-head system one can also obtain different zones with different optical properties on the same marking, which constitute in itself a unique marking (especially when it is in the form of a data matrix). Examples of such data matrices with various multicolor data matrices are described in, e.g., WO 2008/127950 and WO 01/24106, the entire disclosures of which are incorporated by reference herein.
  • the modifying composition may further comprise one or more pigments and/or dyes which absorb in the visible or invisible region of the electromagnetic spectrum and/or may further comprise one or more pigments and/or dyes which are luminescent.
  • suitable pigments and/or dyes which absorb in the visible or invisible region of the electromagnetic spectrum include phthalocyanine derivatives.
  • suitable luminescent pigments and/or dyes include Ianthanide derivatives. The presence of pigment(s) and/or dye(s) will enhance and reinforce the security of the marking against counterfeiting.
  • the modifying composition for use in the present invention may comprise any other components/substances which do not adversely affect the required properties of the modifying composition to any significant extent.
  • the marking according to the present invention is finally obtained by curing and/or polymerizing the composition in the first chiral liquid ciystal state that has been locally modified (in one or more regions) by the application of the modifying composition.
  • the fixing or hardening is preferably performed by irradiation with UV- light, which induces polymerization of the polymerizable groups present in the precursor composition (and optionally in the modifying composition).
  • the marking according to the invention is easy to implement industrially, and reliable.
  • Another advantage of the marking according to the present invention is that the natural random variations inherently present in the printing process according to the present invention can be used as a unique identifier ("fingerprint") which is virtually impossible to reproduce.
  • fingerprint unique identifier
  • the cured and/or polymerized precursor composition in the chiral liquid crystal state is a marking.
  • the modifying composition serves to generate a "marking within/on a marking”.
  • the marking according to the present invention can be incorporated, for example, in a security feature, an authenticity feature, an identification feature or a tracking and tracing feature.
  • a security feature is an overt feature with a 3D effect
  • a marking according to the present invention is prepared as follows:
  • a chiral liquid crystal precursor composition (1 ) was prepared as follows:
  • a chiral dopant compound B of formula (I) shown above i.e., (3R,3aR,6R,6aR)- hexahydrofuro[3,2-b]furan-3,6-diyl bis(4-(4-(acryloyloxy)-3-methoxyberi2oyloxy)-3- methoxy-benzoate) (7.5 g), a nematic compound Al , i.e., benzoic acid, 4-[[[4-[(l -oxo-2- propen- l -yl)oxy]butoxy]carbonyl]oxy]- l,r-(2-methyl-l ,4-phenylene) ester (22.0 g), a nematic compound A2, i.e., 2 -methyl- 1 ,4-phenylene bis(4-(4-(acryloyloxy)butoxy) ⁇ benzoate) (14.0 g), and acetone (49.9 g) were
  • a chiral liquid crystal precursor composition (2) was prepared as follows: A chiral dopant compound B of formula (I) shown above, i.e., (3R,3aR,6R,6aR)-6-(4-(4- (acryIoyloxy)-3-methoxybenzoyloxy)-3-methoxybenzoyloxy)hexahydrofuro[3,2-b]furan- 3-yl 4-(4-(acryloyloxy)benzoyloxy)-3-methoxybenzoate (9.0 g), a nematic compound Al , i.e., benzoic acid, 4-[[[4-[(l-oxo-2-propen-l-yl)oxy]butoxy]carbonyl]oxy]-l, -(2- methyl-l ,4-phenylene) ester (16.0 g), a nematic compound A2, i.e., 2 -methyl- 1 ,4- phenylene bis
  • the chiral liquid crystal precursor composition (1 ) or (2) was then used to print a plain pattern by continuous ink-jet printing on a paper substrate with a dark background.
  • the (first) chiral liquid crystal state was developed from the plain pattern by exposure to an 1R lamp for about 1 to 5 seconds (depending on the substrate).
  • a marking or design was then printed on top of the developed pattern, with a continuous ink-jet printer with a multi-head (three heads).
  • the printing was done sequentially with three solutions, i.e., (a), (b) and (c): (a) a solution (in droplet form) of a resin (5 to 15 % by weight) and of lithium perchlorate (0.6 % by weight) in methyl ethyl ketone or acetone; this solution resulted in an isotropic state in the areas of application;
  • a modified chiral liquid crystal state in the application areas was developed by exposure of the resultant product including the marking to an 1R lamp for about 1 to 5 seconds (depending on the substrate). This resulted locally in a novel anisotropic state different from the first chiral liquid crystal state.
  • the resultant product with the marking printed thereon was then cured by a UV dryer with a mercury low-pressure lamp having a UV irradiance of 10 mW/cm 2 .
  • nematic compound A2 in the above-described procedure the following other compounds may, for example, be employed:

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Finance (AREA)
  • Accounting & Taxation (AREA)
  • Business, Economics & Management (AREA)
  • Manufacturing & Machinery (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Liquid Crystal (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Liquid Crystal Substances (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Credit Cards Or The Like (AREA)
  • Ink Jet (AREA)
  • Ink Jet Recording Methods And Recording Media Thereof (AREA)
  • Duplication Or Marking (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

L'invention porte sur un marquage de polymères cristaux liquides qui peut être obtenu par un procédé qui consiste à appliquer une composition précurseur de cristaux liquides chiraux sur un substrat, à chauffer la composition à un état cristal liquide chiral, à appliquer sur au moins une zone de la composition précurseur une composition de modification, si nécessaire, à chauffer ladite ou lesdites zones pour les amener à un état cristal liquide modifié et, par la suite, à faire durcir et/ou à polymériser le produit ainsi obtenu.
PCT/EP2010/056874 2009-12-08 2010-05-19 Marquage modifié à base de polymères cristaux liquides chiraux WO2011069690A1 (fr)

Priority Applications (20)

Application Number Priority Date Filing Date Title
CN201080055597.XA CN102648097B (zh) 2009-12-08 2010-05-19 以手性液晶聚合物为基础的改性标志
BR112012013585A BR112012013585A2 (pt) 2009-12-08 2010-05-19 marcação modificada com base em polímeros cristalinos líquidos quirais
ES10722053.5T ES2498725T3 (es) 2009-12-08 2010-05-19 Marcaje modificado a base de polímeros de cristales líquidos quirales
EA201290454A EA022293B1 (ru) 2009-12-08 2010-05-19 Модифицированная маркировка на основе хиральных жидкокристаллических полимеров
CA2781460A CA2781460A1 (fr) 2009-12-08 2010-05-19 Marquage modifie a base de polymeres cristaux liquides chiraux
EP10722053.5A EP2509792B1 (fr) 2009-12-08 2010-05-19 Marquage modifié à base de polymères cristaux liquides chiraux
AU2010330332A AU2010330332A1 (en) 2009-12-08 2010-05-19 Modified marking based on chiral liquid crystal polymers
MX2012006205A MX2012006205A (es) 2009-12-08 2010-05-19 Marcado modificado a base de polimeros de cristal liquido quiral.
AP2012006326A AP3477A (en) 2009-12-08 2010-05-19 Modified marking based on chiral liquid crystal polymers
UAA201208214A UA104660C2 (ru) 2009-12-08 2010-05-19 Модифицированная маркировка на основе хиральных жидкокристаллических полимеров
JP2012542408A JP5659430B2 (ja) 2009-12-08 2010-05-19 キラル液晶ポリマーポリマーをベースにした改質されたマーキング
SA110310900A SA110310900B1 (ar) 2009-12-08 2010-12-06 وسم معدل يعتمد على بوليمرات بلورية سائلة كيرالية
UY33083A UY33083A (es) 2009-12-08 2010-12-06 Marcado modificado a base de polimeros de cristal liquido quiral
ARP100104529A AR080628A1 (es) 2009-12-08 2010-12-07 Marcado modificado a base de polimeros de cristal liquido quiral
TW099142551A TW201137092A (en) 2009-12-08 2010-12-07 Modified marking based on chiral liquid crystal polymers
TNP2012000235A TN2012000235A1 (en) 2009-12-08 2012-05-17 Modified marking based on chiral liquid crystal polymers
IL219905A IL219905A0 (en) 2009-12-08 2012-05-21 Modified marking based on chiral liquid crystal polymers
MA34915A MA33778B1 (fr) 2009-12-08 2012-05-31 Marquage modifié à base de polymères cristaux liquides chiraux
ZA2012/04130A ZA201204130B (en) 2009-12-08 2012-06-06 Modified marking based on chiral liquid crystal polymers
HK12113194.3A HK1172296A1 (en) 2009-12-08 2012-12-20 Modified marking based on chiral liquid crystal polymers

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US26765409P 2009-12-08 2009-12-08
US61/267,654 2009-12-08

Publications (1)

Publication Number Publication Date
WO2011069690A1 true WO2011069690A1 (fr) 2011-06-16

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Country Status (25)

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US (1) US8426014B2 (fr)
EP (1) EP2509792B1 (fr)
JP (1) JP5659430B2 (fr)
KR (1) KR20120104568A (fr)
CN (1) CN102648097B (fr)
AP (1) AP3477A (fr)
AR (1) AR080628A1 (fr)
AU (1) AU2010330332A1 (fr)
BR (1) BR112012013585A2 (fr)
CA (1) CA2781460A1 (fr)
CL (1) CL2012001499A1 (fr)
CO (1) CO6541581A2 (fr)
EA (1) EA022293B1 (fr)
ES (1) ES2498725T3 (fr)
HK (1) HK1172296A1 (fr)
IL (1) IL219905A0 (fr)
MA (1) MA33778B1 (fr)
MX (1) MX2012006205A (fr)
SA (1) SA110310900B1 (fr)
TN (1) TN2012000235A1 (fr)
TW (1) TW201137092A (fr)
UA (1) UA104660C2 (fr)
UY (1) UY33083A (fr)
WO (1) WO2011069690A1 (fr)
ZA (1) ZA201204130B (fr)

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JP2014005402A (ja) * 2012-06-26 2014-01-16 Kishu Giken Kogyo Kk インクジェット用インク
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WO2015004129A1 (fr) 2013-07-10 2015-01-15 Sicpa Holding Sa Marquage comprenant un code imprimable et une couche de polymère de cristal liquide chiral
WO2015188890A1 (fr) 2014-06-10 2015-12-17 Sicpa Holding Sa Substrat présentant un marquage fragmenté
US9834031B2 (en) 2012-12-20 2017-12-05 Sicpa Holding Sa Chiral liquid crystal polymer layer or pattern comprising randomly distributed craters therein
US9987866B2 (en) 2014-03-31 2018-06-05 Sicpa Holding Sa Marking comprising a chiral liquid crystal polymer and a luminescent substance

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UA103132C2 (ru) * 2009-12-08 2013-09-10 Сікпа Холдінг Са Маркировка на основе модифицированных хиральных жидкокристаллических полимеров
AU2010330333A1 (en) * 2009-12-08 2012-06-21 Sicpa Holding Sa Marking based on chiral liquid crystal polymers
BR112012013141A2 (pt) * 2009-12-08 2017-04-04 Sicpa Holding Sa marcação de polímero de cristal líquido quiral
US8613507B2 (en) * 2010-10-18 2013-12-24 Xerox Corporation Curable phase change inks containing functionalized isosorbides
US8844801B2 (en) * 2010-11-26 2014-09-30 International Business Machines Corporation Identification and trace of items within an assembly or manufacturing process
AR086508A1 (es) 2011-05-27 2013-12-18 Sicpa Holding Sa Sustrato con una marcacion de polimero de cristal liquido modificado
KR20150013896A (ko) * 2012-05-25 2015-02-05 캠브리지 엔터프라이즈 리미티드 습윤 중합체 용액 상의 액정 액적 레이저 공진기의 프린팅 및 이로부터 제조된 생성물
TW201520216A (zh) 2013-10-21 2015-06-01 Sicpa Holding Sa 對掌性摻雜物與使用聚合性液晶材料標記之識別法及鑑別法
US20170228632A1 (en) * 2016-02-05 2017-08-10 Entrust Datacard Corporation Identification documents with radiation curable material and related methods
GB201803979D0 (en) * 2018-03-13 2018-04-25 Johnson Matthey Plc Security device, method of making a security device and method of authenticating a product

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Cited By (9)

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Publication number Priority date Publication date Assignee Title
JP2013087109A (ja) * 2011-10-21 2013-05-13 Dic Corp 重合性キラル化合物
JP2014005402A (ja) * 2012-06-26 2014-01-16 Kishu Giken Kogyo Kk インクジェット用インク
JP2014005401A (ja) * 2012-06-26 2014-01-16 Kishu Giken Kogyo Kk インクジェット用インク
US9834031B2 (en) 2012-12-20 2017-12-05 Sicpa Holding Sa Chiral liquid crystal polymer layer or pattern comprising randomly distributed craters therein
WO2015004129A1 (fr) 2013-07-10 2015-01-15 Sicpa Holding Sa Marquage comprenant un code imprimable et une couche de polymère de cristal liquide chiral
US9579922B2 (en) 2013-07-10 2017-02-28 Sicpa Holding Sa Marking comprising a printable code and a chiral liquid crystal polymer layer
US9987866B2 (en) 2014-03-31 2018-06-05 Sicpa Holding Sa Marking comprising a chiral liquid crystal polymer and a luminescent substance
WO2015188890A1 (fr) 2014-06-10 2015-12-17 Sicpa Holding Sa Substrat présentant un marquage fragmenté
US10565485B2 (en) 2014-06-10 2020-02-18 Sicpa Holding Sa Substrate with a fragmented marking thereon

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UY33083A (es) 2011-06-01
EP2509792B1 (fr) 2014-07-02
SA110310900B1 (ar) 2014-04-14
IL219905A0 (en) 2012-07-31
HK1172296A1 (en) 2013-04-19
TN2012000235A1 (en) 2013-12-12
JP5659430B2 (ja) 2015-01-28
AR080628A1 (es) 2012-04-25
CO6541581A2 (es) 2012-10-16
EA022293B1 (ru) 2015-12-30
TW201137092A (en) 2011-11-01
KR20120104568A (ko) 2012-09-21
UA104660C2 (ru) 2014-02-25
AU2010330332A1 (en) 2012-06-21
BR112012013585A2 (pt) 2017-03-28
CA2781460A1 (fr) 2011-06-16
JP2013512801A (ja) 2013-04-18
EA201290454A1 (ru) 2013-01-30
CL2012001499A1 (es) 2012-10-05
AP2012006326A0 (en) 2012-06-30
MX2012006205A (es) 2012-06-28
AP3477A (en) 2015-12-31
ZA201204130B (en) 2013-09-25
EP2509792A1 (fr) 2012-10-17
CN102648097B (zh) 2015-02-04
US20110135853A1 (en) 2011-06-09
CN102648097A (zh) 2012-08-22
ES2498725T3 (es) 2014-09-25
US8426014B2 (en) 2013-04-23
MA33778B1 (fr) 2012-11-01

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