WO2006100201A1 - Sicherheitskit und sicherheitstinte - Google Patents
Sicherheitskit und sicherheitstinte Download PDFInfo
- Publication number
- WO2006100201A1 WO2006100201A1 PCT/EP2006/060768 EP2006060768W WO2006100201A1 WO 2006100201 A1 WO2006100201 A1 WO 2006100201A1 EP 2006060768 W EP2006060768 W EP 2006060768W WO 2006100201 A1 WO2006100201 A1 WO 2006100201A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- security
- ink
- marking substance
- colorant
- kit according
- Prior art date
Links
Classifications
-
- 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
Definitions
- the present invention relates to a security kit containing a security ink and a decoder substrate, wherein the security ink contains a colorant and a marking substance and colorant and marking substance have opposite solubilities and wherein the decoder substrate is capable of receiving the marking substance.
- counterfeit protection is the use of additional secondary information that is unobservable to the naked eye because of its inconspicuous nature.
- organic molecules which can be excited to fluorescence in printing processes or in printing fluids, whereby the security against counterfeiting is likewise increased.
- these methods have the disadvantage that they either require a very high expenditure on equipment or, because of their low specificity, can not provide the sharp delimitation necessary for precise identification.
- the present invention relates to a security kit containing a security ink and a decoder substrate, wherein the security ink contains at least one colorant and at least one marking substance and colorant and marking substance have opposite solubilities and wherein the decoder substrate is capable of receiving the marking substance.
- the security ink contains at least one colorant and at least one marking substance and colorant and marking substance have opposite solubilities and wherein the decoder substrate is capable of receiving the marking substance.
- colorants all colorants are generally suitable, which are used for example in inks.
- colorants which are very readily soluble in water but difficult or insoluble in hydrocarbons, such as, for example, toluene, acetone, chloroform, ligroin, hexane, cyclohexane, acetoacetic ester, diethyl ether, ethanol, methanol or methylene chloride.
- colorants are Cl. Reactive Black 8 and 31, Cl. Reactive Red 23, 120, 141 and 180, Cl. Direct Blue 86 and 199, Cl. Direct Yellow 86 and 132, Cl. Direct Black 168, Cl. Acid Yellow 23, Cl. Acid Red 52, Cl. Acid Black 194 and Cl. Food Black 2.
- Marking substances in the sense of the present application are, for example, soluble substances, such as water-soluble dyes such as Cl. Acid Yellow 83 or soluble fluorescent compounds, especially optical brighteners, or organic compounds, which in an azo coupling reaction as
- Coupling component i.e., form by reaction with a diazonium salt an azo dye.
- Preferred optical brighteners are, in particular, commercially available products which belong, for example, to the diaminostilbenedisulfonic acids, heteroaromatic ethylene endevates, coumarins, diarylpyrazolines, naphthalic imides, quinolones or benzoxazole, benzisoxazole and benzimidazole systems.
- strongly fluorescent compounds from the product classes of triazoles and benzothiazoles can be used with advantage.
- Coupling components which can act as marking substances in the context of the present invention are derived, in particular, from the series of pyridones, pyrazolones, Aminobenzene derivatives, hydroxybenzene derivatives, aminonaphthalene derivatives and hydroxynaphthalene derivatives.
- Preferred marking substances in the context of the present application are water-insoluble compounds, such as commercially available optical brighteners for plastics and synthetic fibers, such as, for example, Cl. Fluorescent Brightener 127, 184, 199 and 393, as well as other strongly fluorescent substances, which are free of water-solubilizing substituents such as sulfonic acid or carboxylic acid groups (for example Cl. Solvent Yellow 160), and in particular water-soluble substances, such as commercial optical brightener for
- Cellulosic fibers such as cotton and paper such as Cl.
- Colorant and marker must have opposite solubilities. In the context of the present invention, this means that if the colorant is, for example, water-insoluble, the marking substance must be water-soluble and that the marking substance must be water-insoluble if the colorant is water-soluble.
- the claimed security inks are preferably aqueous inks containing a water-insoluble colorant and, accordingly, a water-soluble marking substance.
- Particularly preferred safeness inks are commercially available carbon black inks containing as a marker a fluorescent compound or an organic compound capable of acting as a coupling component in an azo coupling reaction.
- soot inks, which as a marker substance a mixture of fluorescent compound and an organic compound, which in an azo coupling reaction as
- Coupling component can contain, are particularly preferred.
- the content of marking substance is preferably 0.01 to 2 wt.%, Based on the total weight of the security ink.
- a decoder substrate is understood as meaning a substrate which can receive the marking substance and on which the marking substance is visible or can be made visible. It is included here that the decoder substrate is absorbent and thus can bind water or organic liquids in which the marking substance is dissolved.
- Preferred decoder substrates are flat textile or non-textile substrates. Particularly preferred flat textile substrates are, for example, those of cellulose, cotton, wool, silk, polyamide, polyacrylonitrile, polypropylene or polyester. Particularly preferred flat non-textile substrates are, for example, those of paper, polyester, polyuretane, rubber, nitrocellulose and leather.
- a most preferred decoder substrate is filter paper.
- the security kit according to the invention is advantageously used in such a way that the security ink is used to describe or print a write-on or printable substrate, for example paper or a planar plastic substrate. If the document created in this way is to be checked for authenticity, the marking substance is transferred to the decoder substrate from a small point in the font or print, where it is visible or made visible there. The transfer and visualization of the marking substance is dependent on this. If, for example, a water-soluble fluorescent compound is used as the marking substance, a preferred decoder substrate is filter paper which is moistened with water and brought into intimate contact with the substrate to be tested for a few seconds. The marking substance diffused on the decoder substrate can then be identified by exposure to UV light and assignment of the chromatic fluorescence.
- an organic compound which can act as a coupling component in an azo coupling reaction is used as the marking substance, then a transfer to a moistened filter paper is likewise suitable. There, the contact then takes place with a suitable diazonium salt (for example a commercially available fast dyeing salt) and the characterization of the developed azo dye. Depending on the marking substance are also further detection methods used. An example is NIR spectroscopy.
- the safety kit according to the invention can in addition to security ink and
- Decoder substrate also contain other agents.
- Such further agents are, for example, agents which are necessary for the detection of the marking substance, that is, for example, diazonium salts (fast dyeing salts) for the detection of an organic marking substance.
- the claimed safety inks are known in part.
- the abstract of KR 10 2004 0060393 A describes inks which contain not only insoluble pigments but also fluorescent dyes.
- the present invention thus also relates to an aqueous security ink containing at least one water-insoluble colorant and an organic compound capable of acting as a coupling component in an azo coupling reaction.
- Preferred water-insoluble colorants and organic compounds capable of acting as a coupling component in an azo coupling reaction are the colorants or compounds referred to above as preferred.
- the security inks according to the invention contain colorants in amounts of, for example, from 0.1% by weight to 50% by weight, preferably in amounts of from 1% by weight to 30% by weight and more preferably in amounts of from 1% by weight to 15 wt .-% based on the total weight of the ink.
- the organic compound capable of acting as a coupling component in an azo coupling reaction must be contained in the security ink of the present invention at least in such an amount as to allow reliable detection of the azo dye developed on the decoder substrate. Usually are to 0.01 to 2 wt.%, Based on the total weight of the security ink sufficient.
- the security inks according to the invention may of course also contain other auxiliaries and additives which are customary in inks. The skilled person is informed about these means.
- the advantages of the security kit according to the invention are, in particular, the simple application, since testing for the authenticity of a document can be carried out practically everywhere without major technical effort. Likewise, no special requirements for the creation of the information carrier necessary because z. B. for the creation of marked documents by the method described commercial printer paper and printer can be used without further pretreatment. On the other hand, the mark can not be detected without the downstream identification by means of decoder substrate, so that it is not immediately apparent whether there is a marked product at all.
- Example 2 To 100 g of a commercially available pigment ink based on Cl. Pigment Blue 15: 4, Cl. Pigment Red 122 and Cl. Pigment Yellow 74 is 0.1 g of Cl. Fluorescent Brightener 260 given. The authenticity of a document printed with this ink is ensured by being one with little water moistened cellulose filter paper for approx. 5 seconds on a printed area of the document. Under UV light, the impression is made visible on the cellulose filter paper.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BRPI0609139-3A BRPI0609139A2 (pt) | 2005-03-19 | 2006-03-15 | kit de segurança e tinta de segurança |
CA002602001A CA2602001A1 (en) | 2005-03-19 | 2006-03-15 | Security kit and security ink |
JP2008501308A JP2008533267A (ja) | 2005-03-19 | 2006-03-15 | セキュリティキットおよびセキュリティインク |
US11/908,978 US20080163777A1 (en) | 2005-03-19 | 2006-03-15 | Security Kit and Security Ink |
EP06725084A EP1863887A1 (de) | 2005-03-19 | 2006-03-15 | Sicherheitskit und sicherheitstinte |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005012747.9 | 2005-03-19 | ||
DE102005012747 | 2005-03-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006100201A1 true WO2006100201A1 (de) | 2006-09-28 |
Family
ID=36130077
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/060768 WO2006100201A1 (de) | 2005-03-19 | 2006-03-15 | Sicherheitskit und sicherheitstinte |
Country Status (8)
Country | Link |
---|---|
US (1) | US20080163777A1 (de) |
EP (1) | EP1863887A1 (de) |
JP (1) | JP2008533267A (de) |
CN (1) | CN101128552A (de) |
BR (1) | BRPI0609139A2 (de) |
CA (1) | CA2602001A1 (de) |
TW (1) | TW200641070A (de) |
WO (1) | WO2006100201A1 (de) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6477064B2 (ja) * | 2015-03-12 | 2019-03-06 | コニカミノルタ株式会社 | 水系インクおよびインクジェット捺染方法 |
KR102585243B1 (ko) * | 2021-05-26 | 2023-10-05 | 한국생산기술연구원 | 위변조 방지를 위한 형광 잉크 조성물, 형광 잉크 조성물의 제조 방법 및 잉크 조성물을 이용한 위변조를 방지하는 보안 문서 |
WO2024058928A1 (en) * | 2022-09-14 | 2024-03-21 | Eastman Kodak Company | Printing fluorescent aqueous colored inks and methods of inkjet printing |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5720801A (en) * | 1996-11-06 | 1998-02-24 | Nadan; Wendy | Water resistant security ink composition |
WO2000053597A2 (en) * | 1999-03-10 | 2000-09-14 | Ciba Specialty Chemicals Holding Inc. | Benzofuran-2-ones as colorants for organic materials |
EP1067155A1 (de) * | 1998-03-25 | 2001-01-10 | Nippon Kayaku Kabushiki Kaisha | Neue anthrapyridonverbindungen, magentatintenzusammensetzungen auf wasserbasis sowie verfahren zur tintenstrahlaufzeichnung |
US6413305B1 (en) * | 2000-02-07 | 2002-07-02 | The Standard Register Company | Thermochromic ink composition |
US20020096086A1 (en) * | 2000-09-21 | 2002-07-25 | Greig Chisholm | Azo orange pigment composition |
US20020107309A1 (en) * | 1995-06-13 | 2002-08-08 | Joseph Malanga | Water-based intaglio printing ink |
US6491749B1 (en) * | 1998-10-21 | 2002-12-10 | Ciba Specialty Chemicals Corporation | Core-extended perylene bisimides |
DE10259033A1 (de) * | 2002-12-17 | 2004-07-08 | Heinz Prof. Dr. Langhals | Composite aus Erdalkali-Erdmetallionen und organischen Farbstoffen, ein neuer Typ von Farbpigmenten |
-
2006
- 2006-03-15 CN CNA2006800063771A patent/CN101128552A/zh active Pending
- 2006-03-15 CA CA002602001A patent/CA2602001A1/en not_active Abandoned
- 2006-03-15 BR BRPI0609139-3A patent/BRPI0609139A2/pt not_active Application Discontinuation
- 2006-03-15 EP EP06725084A patent/EP1863887A1/de not_active Withdrawn
- 2006-03-15 WO PCT/EP2006/060768 patent/WO2006100201A1/de active Application Filing
- 2006-03-15 JP JP2008501308A patent/JP2008533267A/ja not_active Withdrawn
- 2006-03-15 US US11/908,978 patent/US20080163777A1/en not_active Abandoned
- 2006-03-16 TW TW095109013A patent/TW200641070A/zh unknown
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020107309A1 (en) * | 1995-06-13 | 2002-08-08 | Joseph Malanga | Water-based intaglio printing ink |
US5720801A (en) * | 1996-11-06 | 1998-02-24 | Nadan; Wendy | Water resistant security ink composition |
EP1067155A1 (de) * | 1998-03-25 | 2001-01-10 | Nippon Kayaku Kabushiki Kaisha | Neue anthrapyridonverbindungen, magentatintenzusammensetzungen auf wasserbasis sowie verfahren zur tintenstrahlaufzeichnung |
US6491749B1 (en) * | 1998-10-21 | 2002-12-10 | Ciba Specialty Chemicals Corporation | Core-extended perylene bisimides |
WO2000053597A2 (en) * | 1999-03-10 | 2000-09-14 | Ciba Specialty Chemicals Holding Inc. | Benzofuran-2-ones as colorants for organic materials |
US6413305B1 (en) * | 2000-02-07 | 2002-07-02 | The Standard Register Company | Thermochromic ink composition |
US20020096086A1 (en) * | 2000-09-21 | 2002-07-25 | Greig Chisholm | Azo orange pigment composition |
DE10259033A1 (de) * | 2002-12-17 | 2004-07-08 | Heinz Prof. Dr. Langhals | Composite aus Erdalkali-Erdmetallionen und organischen Farbstoffen, ein neuer Typ von Farbpigmenten |
Also Published As
Publication number | Publication date |
---|---|
US20080163777A1 (en) | 2008-07-10 |
CA2602001A1 (en) | 2006-09-28 |
JP2008533267A (ja) | 2008-08-21 |
TW200641070A (en) | 2006-12-01 |
EP1863887A1 (de) | 2007-12-12 |
CN101128552A (zh) | 2008-02-20 |
BRPI0609139A2 (pt) | 2010-02-23 |
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