GB2258660A - Anti-stokes luminescent material - Google Patents

Anti-stokes luminescent material Download PDF

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Publication number
GB2258660A
GB2258660A GB9117543A GB9117543A GB2258660A GB 2258660 A GB2258660 A GB 2258660A GB 9117543 A GB9117543 A GB 9117543A GB 9117543 A GB9117543 A GB 9117543A GB 2258660 A GB2258660 A GB 2258660A
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United Kingdom
Prior art keywords
materials
material according
particles
stokes
ppm
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
GB9117543A
Other versions
GB9117543D0 (en
GB2258660B (en
Inventor
Robin Bratchley
Derek Michael Wallace
Ranby Peter Whitten
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
De la Rue International Ltd
Original Assignee
Thomas De la Rue and Co Ltd
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.)
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Publication date
Application filed by Thomas De la Rue and Co Ltd filed Critical Thomas De la Rue and Co Ltd
Priority to GB9117543A priority Critical patent/GB2258660B/en
Publication of GB9117543D0 publication Critical patent/GB9117543D0/en
Publication of GB2258660A publication Critical patent/GB2258660A/en
Application granted granted Critical
Publication of GB2258660B publication Critical patent/GB2258660B/en
Priority to HK79396A priority patent/HK79396A/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D11/00Inks
    • C09D11/50Sympathetic, colour changing or similar inks
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B42BOOKBINDING; ALBUMS; FILES; SPECIAL PRINTED MATTER
    • B42DBOOKS; 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
    • B42D25/00Information-bearing cards or sheet-like structures characterised by identification or security features; Manufacture thereof
    • B42D25/30Identification or security features, e.g. for preventing forgery
    • B42D25/36Identification or security features, e.g. for preventing forgery comprising special materials
    • B42D25/378Special inks
    • B42D25/382Special inks absorbing or reflecting infrared light
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/08Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
    • C09K11/77Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
    • C09K11/7766Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals
    • C09K11/7767Chalcogenides
    • C09K11/7769Oxides
    • C09K11/7771Oxysulfides
    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06KGRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
    • G06K19/00Record carriers for use with machines and with at least a part designed to carry digital markings
    • G06K19/06Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code
    • G06K19/08Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code using markings of different kinds or more than one marking of the same kind in the same record carrier, e.g. one marking being sensed by optical and the other by magnetic means
    • G06K19/10Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code using markings of different kinds or more than one marking of the same kind in the same record carrier, e.g. one marking being sensed by optical and the other by magnetic means at least one kind of marking being used for authentication, e.g. of credit or identity cards
    • G06K19/14Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code using markings of different kinds or more than one marking of the same kind in the same record carrier, e.g. one marking being sensed by optical and the other by magnetic means at least one kind of marking being used for authentication, e.g. of credit or identity cards the marking being sensed by radiation

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Theoretical Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Luminescent Compositions (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

An anti-Stokes luminescent material is prepared from a fused mixture of rare earth compounds and, if necessary, other components, is in the form of particles no more than 40 mu m in size and has substantially the same luminescence as the fused mixture. The material is preferably doped with yttrium oxysulphide, and is used in inks.

Description

LUMINESCENT MATERIALS AND THEIR PREPARATION This invention relates to materials that can be used, fo exanple, as markers for authenticating itens such as security documents, and to their preparation.
Luminescent materials such as fluorescent and phosphorescent materials are commonly used in banknotes and the like for security verification purposes. The commercially-used luminophors obey Stokes Law, in that their emissions are at a lower energy than that of the exciting radiation. For example, such materials when illuminated with ultraviolet radiation will emit in the visible.
Anti-Stckes cr, as they are otherwise known, "upconverting" materials emit light (visible or ultraviolet) which has a shorter wavelength than the activating radiation. For the purpose of this specification, Anti-Stokes materials absorb infrared radiation, typically fro 700 to 1300 nm, and emit in the visible. Anti-Stokes materials emit photons at higher energy, and this can arise if two or more incident photons result in ore eritte ct if higher energy).
Anti-Stcr;es materials ha- seer. lim ted application to security items.
Inorganic luminescent pigments are normally refractory solids and, if the particle size is reduced by grinding, then their luminescent efficiency decreases rapidly, as is well known. Unfortunately, the smallest acceptable anti Stokes particle size previously available is much larger than is normally acceptable for security printing inks. It has not hitherto been possible to rake satisfactory ink formulations which contain anti-Stokes materials suitable for the main security printing methods, i.e. intaglio, letterpress or lithography, owing to their requirement for small particles.
For use in currency, particularly severe demands are placed on inks. The inks must retain their properties for the life of the document, withstanding the rigours and challenges of handling, wetting and contamination.
Similarly stringent properties must also apply to other security documents which have a long life and whose value is associated with the integrity of the document.
Security documents by their very nature need to incorporate a variety of different measures in order to defeat counterfeiting. At one extreme, visual measures are designed to be seen with the naked eye. At the other extreme, sophisticated and expensive detectors may be employed, say attached to banknote sorting equipment, to validate banknotes and the like. Many of these features may be invisible under normal viewing conditions.
US-A-4047033 discloses documents including anti-Stokes fluoride materials. Such materials are generally unsuitable for security documents, however, since they are liable to hydrolysis which causes a reduction of their luminescence, and because they are difficult to produce in finely particulate form, i.e. less than 20 4m in size. The particles disclosed in US-A-4047033 are adapted for screen inks, and are therefore relatively large.
GB-A-2089385 discloses ferrite, perovskite and garnet-type storage phosphor materials for security documents that absorb in the IR, emitting in the UC.
AU-A-0562509 and AU-A-0571276 describe fluoride, oxide or mixed rare earth oxyfluoride anti-Stokes luminescent materials and their use in security documents. Inks are not described. Some of such materials are liable to hydrolysis; they are difficult to reduce to a suitably small particle size while maintaining fluorescence efficiency. The former document discloses precipitation, sieving and crushing, to obtain small particles.
US-A-4387112 discloses credit cards marked with inorganic storage phosphors, e.g. a mixed phosphor such as SrS(Eu,Sm). They are used in finely-divided form, apparently after grinding. The luminescent properties of almost all phosphors are adversely affected by grinding.
According to the present invention, an anti-Stokes luminescent material cr,mprises a doped rare earth compound that is in the form cf particles no greater than 40 jim in size and whose luminescence is substantially at least the same as that of a fused mass of the component compounds.
A material of the invention is in the form of particles which are suitable for use in printing by intaglio, letterpress or offset lithography. For this purpose, the particles have a maximum diameter of no more than 40 pm, more preferably no more than 20 pm, and most preferably below 10 Mm, e.g. 1 to 5 Mm or even 1 to 2 jim.
Particles of such a size can be produced, without grinding, by a process in which, for a doped rare earth oxysulphide, oxides of the rare earths are fused with sulphides or elemental sulphur, the fused mass is leached with water to extract soluble residues, and dried as a powder. Some milling may then be appropriate, depending on the desired particle size.
Although, more generally, the invention relates to any anti-Stokes material that is prepared from a fused mixture of rare earth compounds and, if necessary, other components, a particularly suitable material is doped yttrium oxysulphide, in which the dopants comprise, by weight of the oxysulphide, 4 to 50t of one or more of Er, Yb and Ho, and 1 to 50 ppm of one or more other lanthanide elements. Such a material is described in another Patent Application filed in the name of Thomas De La Rue and Company Ltd and on the same day, entitled "Luminescent Materials and Their use in Security Documents".
The oxysulphide described in the copending Application has the general chemical composition Y202S:A, where A is a primary rare earth dopant selected from Yb, Er or a mixture of Yb and Er. One such composition, i.e. Y202S:Yb,Er, is usually characterised by green emission on IR stimulation.
The total level of doping is generally no more than 30%, and typically less than 25%. For example, the material comprises 2 to 10 Er and s to 15 b. The weight ratio of Yb to Er ray be approximately 1:3.
Other rare earth elements can have a marked effect on luminescent properties, even when present in very small amounts. The amounts of these elements present must be carefully controlled. In the case cf Y202S:Yb,Er, good results may be achieved if one or more of La, Ce, Pr, Nd, Sm, Eu, Gd, Tb and Dy is present in an amount of less than 3 ppm and, in certain instances, less than 1 ppm. Higher levels of Ho, Tm and Lu can improve luminescent efficiency, e.g. when present at 2-20 ppm.
The purity of the starting materials will determine the performance cf the proA.uct. It is preferred to use at least 99.999% pure yttriu oxide, and 99.99% pure ytterbium and erbium oxides.
The doped oxysulphide may be prepared by firing a blend of, say, BDH Chemicals Ltd. AnalaR quality flux materials with pure yttrium oxide, ytterbium oxide and erbium oxide, e.g. at 11000C for 1 hour. The firing time and temperature may be varied within the ranges 0.5 to 4 hours and 1000 to 1200 C, wile 1050-1150 C and 1-2 hours give consistent resits. A fIrIng schedule of 1 hour at 11000C is suitable on this sza'e.
The ratio of yttrium : ytterblur : erbium in the blend, before firing, may be varied. Some increase in brightness may be obtained by adjusting the ytterbium content.
The value of the materials used in the present invention includes their stability and their high anti Stokes efficiency. They are therefore useful as markers in security documents, for preventing counterfeiting.
Security items are items whose value is established or increased by being difficult to counterfeit or alter fraudulently. Examples of security documents, which may incorporate materials of the invention, are banknotes, currency, share certificates, bonds, passports, driving licences, permits, travel tickets, lottery tickets, plastic credit cards, charge cards, cash withdrawal cards, cheque cards, travellers' cheques and bank cheques, smart cards and remote access control cards.
A security document incorporating a material of the invention may conveniently be prepared by applying an ink containing the material. The security printed item may be a banknote.
The ink will normally be used to print, by letter press, intaglio or offset, invisible designs and security features. Alternatively, the materials may be incorporated into coloured inks, to enhance the anti-counterfeiting level of the printing. This may be done, for example, by incorporating the material into a banknote-numbering ink.
Intaglio and letterpress inks are preferred.
Letterpress can achieve 5 jim of ink film. Intaglio ink printing can give printed thicknesses of, say, 5 to 70 jim.
An ink of the invention comprises, in addition to the anti-Stokes material, conventional components such as a colourant and a vehicle. For example, the ink may be prepared by thoroughly mixing an extender, wax, anti-Stokes material and any other security additives with resins components of an ink vehicle, and a hydrocarbon solvent.
These components are then further dispersed, typically using a triple-roll mill, at a suitable pressure. Once the correct degree of dispersion has been reached, further solvent and other components may be added.
A security document of the invention may be authenticated by irradiation with infrared light, and observation of the visible light thus produced. The means of irradiation may be, for example, a near infrared-emitting gas laser, laser diode or infraredemitting diode. Laser diodes or infrared emitting diodes, for example GaAs(Si) emitting at 940 nm, may conveniently be employed with matching materials. Alternatively, tungsten-halogen light sources, suitably filtered to remove visible light, may be used.
The materials of the invention have relatively narrow absorption and emission bands. The emission of the illuminating source must therefore be matched to the absorbance of the material and, in the case of machine-reading, this must be matched to the detector.
Photodetectors tend te have a ..ide absorption band which may be narrowed by the use of filters or spectral discriminators.
For the purposes of this specification, the ultraviolet, visible and infrared regions cover from 200 to 399 nm, 400 to 699 nm, and 700 to 1300 nm, respectively.
The printed ink may be viewed by exposure with an infrared diode emitting at appro tes 940 nr (peak wavelength) Materials of the invention normally will exhibit a shift of at least 100 nm from the illuminating source, and preferably of 200 nm or more. For example, cn irradiation with an infrared diode emitting at a peak wavelength around 940 nm, it is possible te observe crange, green, yelloworange fluorescences.
An advantage of the invention is that it is not obvious from visible examination of the, say, intaglio printing that the printing has an area responsive emitter. The effect is not obvious in its own right, and there are of course many posible physical effects which might be used. Such an effect is therefore deeply hidden, and it will therefore not be readily detectable by a potential counterfeiter.
In order to disguise the effect of those materials which do not themselves luminesce on exposure to ultraviolet illumination, it is possible to mix normal (Stokes) luminophors with the anti-Stokes material. In certain cases, an IR-activated anti-Stokes luminophor which emits in the visible may cause a fluorescent material of emitting absorbance to emit at a longer wavelength.
A particulate material of the invention has substantially the same luminescence, at a given wavelength, as the fused mixture of compounds from which it may be prepared. The loss of luminescence is preferably no moro than 50%, and more preferably no more than 25%.
The following Examples illustrate the invent on.
"3N's Grade" and "4N's Grade" indicate a purity of respectively 99.9% and 99.99%.
Example 1 The following materials were milled together in a pint size porcelain mill jar with porcelain balls for 2 hours: 78.74 g yttrium oxide (3N's grade) 14.96 g ytterbium oxide (4N's grade) 6.30 g erbium oxide (4N's grade) 250 ml water After milling, the porcelain balls were separated from the slurry of rate earth oxides, the latter was filtered and the mixed rare earth oxides were dried and then sieved.
20 g of this mixed oxide powder was intimately mixed with: 7.48 g potassium fluoride 5.52 g sodium carbonate 5.52 g sulphur and heated at 11000 for 1 holr in a cered alunina cruclk'e. When csa the fused mass .as soaked in water until it softened oon to a fine pc-dr which was then filtered off, washed with more ater, dried and sieved.
This material, on irradiation with IR, emitted green radiation. The material was then milled.
The particle size was determined microscopically and at least 90% of the particles had a maximum diameter of less than 40 jim.
In addition to using the purest available components, the crucible was of recystallised alumina. Contamination was avoided wherever possible.
Ytrrium oxysulphide phosphors are usually fairly resistant to grinding, but can be prepared in fine particle size ranges. Milling can be used to reduce the particle size further but generally such grinding is avoided if possible.
Examples 2 to 5 Doped yttrium oxysulphide phosphors were prepared by the procedure of Example 1. In Example 3, the oxide was of Norwegian origin and supplied by Berkshire Ores Ltd as their "phosphor grade". In Example 4, the oxide was supplied by The Propane Company, as their "phosphor grade".
In Examples 2 and 5, the oxides were from different suppliers.
The rare earth compositions were determined by using an inductively-coupled plasma atomic emission spectrometer and an inductively-coupled plasma mass spectrometer. The results are tabulated below: Element Ex. 2 Ex. 3 Ex. 4 Ex. 5 Y 58.9% 61.1% 61.2% 59.9% Er 4.738 4.878 4.838 4.85% Yb 12.8% 11.0% 10.9% 10.8% Ho 17.3 ppm < 1 ppm < 1 ppm < 1 ppm Tm 7.5 ppm < 1 ppm < 1 ppm 4.7 ppm Lu 8.2 ppm 3.1 ppm 2.5 ppm 4.8 ppm In each case, the La, Gd, Tb and Dy content was each less than 1 ppm, the Nd, Sa and Eu content was each less than 2 ppm, and the Ce and Pr content each less than 3 ppm.
The sulphur content (11.75%) for Example 2 was determined separately, and the oxygen content (11.828) by subtraction.
Particle size determination was made by optical microscopy taking the maximum diameter of the particles and assessing an approximate distribution range and average particle size.
Results are as follows (all values in jim): Example Number Majority Maximum Maximum No. Average ( > 50t) 2 13 5-20 30 5 3 15 10-20 35 5 4 11 6-12 26 4 5 13 6-18 30 4 These sizes are those which result from the preparation without milling. Normally some milling is carried out to reduce the particle range, especially to reduce the size of the larger particles so that the material may be incorporated in an ink formulation. For the above letterpress ink formulations are prepared. These is no significant reduction in luminosity on milling.

Claims (7)

1. An anti-Stokes luminescent material as prepared from a fused mixture of rare earth compounds and, if necessary, other components, that is in the form of particles no more than 40 jim in size and that has substantially the same luminescence as the fused mixture.
2. A material according to claim 1, which comprises doped yttrium oxysulphide.
3. A material according to either preceding claim, in which the average size of the particles is no more than 20 jim.
4. A material according to claim 3, in which the average size of the particles is 1 to 10 m.
5. An ink comprising a material according to any preceding claim, a vehicle and, optionally, a colourant.
6. A security document or authenticated item bearing a material according to any of claims 1 to 4.
7. A method for preparing a material according to any of claims 1 to 4, which comprises leaching the fused mixture with water to extract soluble residues and, if necessary, milling the precipitated product.
GB9117543A 1991-08-14 1991-08-14 Luminescent materials and their preparation Expired - Fee Related GB2258660B (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB9117543A GB2258660B (en) 1991-08-14 1991-08-14 Luminescent materials and their preparation
HK79396A HK79396A (en) 1991-08-14 1996-05-09 Luminescent materials and their preparation

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GB9117543A GB2258660B (en) 1991-08-14 1991-08-14 Luminescent materials and their preparation

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GB2258660A true GB2258660A (en) 1993-02-17
GB2258660B GB2258660B (en) 1995-06-07

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998039392A1 (en) * 1997-03-05 1998-09-11 Riedel-De Haen Gmbh Non-green anti-stokes luminescent substance
EP1117060A1 (en) * 2000-01-10 2001-07-18 Sicpa Holding S.A. Authentication of a security article
US6479133B1 (en) * 1998-02-02 2002-11-12 Giesecke & Devrient Gmbh Document having a value
US6506476B1 (en) * 1998-02-02 2003-01-14 Glesecke & Devrient Gmbh Printed document having a value, with luminescent authenticity feature
US6613137B2 (en) 2000-01-10 2003-09-02 Sicpa Holding S.A. Coating composition, preferably printing ink for security applications, method for producing a coating composition and use of glass ceramics
DE10208397A1 (en) * 2002-02-27 2003-09-11 Honeywell Specialty Chemicals Anti-Stokes phosphor composition
US6731785B1 (en) 1999-07-26 2004-05-04 Cummins-Allison Corp. Currency handling system employing an infrared authenticating system
US6841092B2 (en) 2001-03-16 2005-01-11 Bundesdruckerei Gmbh Anti-stokes fluorescent compositions and methods of use
EP1679549A2 (en) 2005-01-07 2006-07-12 E.I.Du pont de nemours and company Imaging element for use as a recording element and process of using the imaging element
DE102005032831A1 (en) * 2005-06-30 2007-01-04 Bundesdruckerei Gmbh Holmium-doped anti-Stokes phosphors and security features with these phosphors
DE102006047851A1 (en) * 2006-10-10 2008-04-17 Giesecke & Devrient Gmbh Authenticity feature in the form of luminescent substances
WO2008132223A2 (en) * 2007-04-30 2008-11-06 Österreichische Staatsdruckerei Gmbh Use of a luminophore as security feature security printing ink method and device for checking a document and document and security feature
US8328102B2 (en) 2009-12-21 2012-12-11 Honeywell International Inc. Method and authentication apparatus for authenticating value documents
EP2570468A1 (en) 2011-09-13 2013-03-20 Bundesdruckerei GmbH Anti-stokes luminescent substances and use thereof in security documents
WO2015086497A1 (en) * 2013-12-10 2015-06-18 Polysecure Gmbh Marked layer structure, process for producing it and use thereof
DE102016120979A1 (en) 2016-11-03 2018-05-03 Bundesdruckerei Gmbh Method for checking the authenticity of a security feature and arrangement for checking the authenticity of a security document with a security feature
DE102019122010A1 (en) * 2019-08-15 2021-02-18 Polysecure Gmbh Article comprising fluorescent marker particles and methods of identifying the same

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111815334A (en) * 2020-06-22 2020-10-23 深圳市丰腾防伪技术有限公司 Anti-counterfeiting tracing method based on cipher

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GB650459A (en) * 1946-05-03 1951-02-28 Franz Urbach Improvements in photographic recording and luminescent materials therefor
EP0092240A1 (en) * 1982-04-20 1983-10-26 Fuji Photo Film Co., Ltd. Radiation image storage panel
US4586811A (en) * 1982-04-23 1986-05-06 Ricoh Company, Ltd. Confidential document reproduction prevention method

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Publication number Priority date Publication date Assignee Title
GB650459A (en) * 1946-05-03 1951-02-28 Franz Urbach Improvements in photographic recording and luminescent materials therefor
EP0092240A1 (en) * 1982-04-20 1983-10-26 Fuji Photo Film Co., Ltd. Radiation image storage panel
US4586811A (en) * 1982-04-23 1986-05-06 Ricoh Company, Ltd. Confidential document reproduction prevention method

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6802992B1 (en) 1997-03-05 2004-10-12 Wieczoreck Juergen Non-green anti-stokes luminescent substance
WO1998039392A1 (en) * 1997-03-05 1998-09-11 Riedel-De Haen Gmbh Non-green anti-stokes luminescent substance
US6479133B1 (en) * 1998-02-02 2002-11-12 Giesecke & Devrient Gmbh Document having a value
US6506476B1 (en) * 1998-02-02 2003-01-14 Glesecke & Devrient Gmbh Printed document having a value, with luminescent authenticity feature
US6731785B1 (en) 1999-07-26 2004-05-04 Cummins-Allison Corp. Currency handling system employing an infrared authenticating system
US6613137B2 (en) 2000-01-10 2003-09-02 Sicpa Holding S.A. Coating composition, preferably printing ink for security applications, method for producing a coating composition and use of glass ceramics
AU775293B2 (en) * 2000-01-10 2004-07-29 Sicpa Holding S.A. Article authentication
WO2001052175A1 (en) * 2000-01-10 2001-07-19 Sicpa Holding S.A. Article authentication
EP1117060A1 (en) * 2000-01-10 2001-07-18 Sicpa Holding S.A. Authentication of a security article
DE10113267B4 (en) 2001-03-16 2019-05-09 Bundesdruckerei Gmbh Use of an anti-Stokes phosphor in security documents
US6841092B2 (en) 2001-03-16 2005-01-11 Bundesdruckerei Gmbh Anti-stokes fluorescent compositions and methods of use
DE10208397A1 (en) * 2002-02-27 2003-09-11 Honeywell Specialty Chemicals Anti-Stokes phosphor composition
EP1679549A2 (en) 2005-01-07 2006-07-12 E.I.Du pont de nemours and company Imaging element for use as a recording element and process of using the imaging element
DE102005032831A1 (en) * 2005-06-30 2007-01-04 Bundesdruckerei Gmbh Holmium-doped anti-Stokes phosphors and security features with these phosphors
US8367188B2 (en) 2006-10-10 2013-02-05 Giesecke & Devrient Gmbh Authenticity mark in the form of luminescent substances
DE102006047851A1 (en) * 2006-10-10 2008-04-17 Giesecke & Devrient Gmbh Authenticity feature in the form of luminescent substances
WO2008132223A2 (en) * 2007-04-30 2008-11-06 Österreichische Staatsdruckerei Gmbh Use of a luminophore as security feature security printing ink method and device for checking a document and document and security feature
WO2008132223A3 (en) * 2007-04-30 2009-01-15 Oesterreichische Staatsdrucker Use of a luminophore as security feature security printing ink method and device for checking a document and document and security feature
US8328102B2 (en) 2009-12-21 2012-12-11 Honeywell International Inc. Method and authentication apparatus for authenticating value documents
EP2570468A1 (en) 2011-09-13 2013-03-20 Bundesdruckerei GmbH Anti-stokes luminescent substances and use thereof in security documents
WO2015086497A1 (en) * 2013-12-10 2015-06-18 Polysecure Gmbh Marked layer structure, process for producing it and use thereof
DE102016120979A1 (en) 2016-11-03 2018-05-03 Bundesdruckerei Gmbh Method for checking the authenticity of a security feature and arrangement for checking the authenticity of a security document with a security feature
WO2018083017A1 (en) 2016-11-03 2018-05-11 Bundesdruckerei Gmbh Method for the authentication of a security feature and assembly for the authentication of a security document having a security feature
DE102019122010A1 (en) * 2019-08-15 2021-02-18 Polysecure Gmbh Article comprising fluorescent marker particles and methods of identifying the same

Also Published As

Publication number Publication date
HK79396A (en) 1996-05-17
GB9117543D0 (en) 1991-10-02
GB2258660B (en) 1995-06-07

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