Marked coating composition and method for its authentication

Patent metadata

Field	Value
Publication number	US-2015132543-A1
Application number	US-201214361618-A
Country	US
Kind code	A1
Filing date	Nov 28, 2012
Priority date	Nov 30, 2011
Publication date	May 14, 2015
Grant date	—

Abstract

This invention relates to the field of authentication of coating compositions such as varnishes, inks and paints, and it is particularly useful in the field of authentication of such coating compositions when applied to substrates like banknotes or other valuable documents. It is particularly directed to a marked coating composition. e.g. an ink, that is marked with a marker (taggant) such as to allow for its authentication, and a method for authenticating such a marked coating composition. The marking is achieved by covalently binding a taggant to a coating composition component. e.g. such used for security documents. The taggant, which is not extractable through usual chemical treatments like washing methods or the use of solvents, can be detected and identified upon thermally induced chemical fragmentation with a PY-GC-MS apparatus. The marked ink or the marked substrate is thus authenticated as belonging to a particularly marked ink, varnish or batch.

First claim

1 . A composition, which is a marked coating composition (1), comprising
(i) a marked non-extractable component (5) comprising an oligomeric or polymeric moiety (2a) and at least one marker moiety (3a) bonded to the moiety (2a) via a covalent linking group (4); or (ii) an oligomeric or polymeric component (2) and at least one marker (3) comprising a marker moiety (3a) and a group capable of forming a linking group (4) to obtain the component (5) upon curing the composition (1); wherein the amount of the marker moiety (3a), based on the composition (1), is 0.001-1 wt.-%.

2 . The composition of claim 1 , wherein one marker moiety (3a) is present.

3 . The composition of claim 1 , wherein two or more different marker moieties (3a) are present, and preferably in a defined molecular ratio.

4 . The composition of claim 1 , wherein the moiety derived from the marker (3) and comprising the marker moiety (3a) and the covalent linking group (4) is selected from

wherein
R each independently is selected from H, D (deuterium), T (tritium), C 1-18 -alkyl, C 1-18 -alkenyl, C 1-18 -alkynyl, C 3-12 -cycloalkyl, C 3-12 -cycloalkenyl, C 1-12 -heterocycloalkyl, C 7-12 -aralkyl, Hal, CH 2 Hal, CHHal 2 , CHal 3 , CN, CXXR 2 , OR 2 , SR 2 , NR 2 R 3 , —N═N—Ar, ═N—NR 2 Ar, SiR 4 R 5 R 6 , X—P(X)(XR 2 )(XR 3 ), P(X)(XR 2 )(XR 3 ), SOR 2 , SO 2 R 2 , phenyl substituted with 1-3 groups R 2 different from H, or a 5-8-membered heteroaromatic group having at least on of O, S, N, NH and N(C 1-18 -alkyl) in the ring;
or two adjacent groups R separated by 2 or 3 carbon atoms together form a moiety selected from

R 1 each independently is selected from H, D (deuterium), T (tritium), C 1-18 -alkyl, Hal, CH 2 Hal, CHHal 2 , CHal 3 , CN, CXXR 2 , OR 2 , SR 2 , NR 2 R 3 , SiR 4 R 5 R 6 , P(X)(XR 2 )(XR 3 ), X—P(X)(XR 2 )(XR 3 ), SOR 2 and SO 2 R 2 ;
or in formulae (VIa)-(VId) two geminal groups R 1 , together with the carbon atom to which they are bound, each independently are C═O, C═NR 2 or C═S;

R 2 , R 3 each independently is selected from H, D (deuterium), C 1-18 -alkyl, C 1-18 -alkenyl, C 1-18 -alkynyl, C 3-12 -cycloalkyl, C 3-12 -cycloalkenyl, C 1-12 -heterocycloalkyl, C 7-12 -aralkyl, CH 2 Hal, CHHal 2 , CHal 3 , SiR 4 R 5 R 6 , phenyl and a 5-8-membered heteroaromatic group having at least on of O, S, N, NH and N(C 1-18 -alkyl) in the ring;
R 4 , R 5 and R 6 each independently are selected from C 1-18 -alkyl, O(C 1-18 -alkyl) and N(C 1-18 -alkyl);
Hal is F, Cl, Br or I;
Ar is an aromatic group;
X is O, NH, N(C 1-18 -alkyl) or S; and
m, n, p each are a number in the range of 0-20; and
(i) at least one, preferably one to four, and more preferably one or two, group(s) R is/are a covalent linking group (4) linking the marker moiety (3a) to the oligomeric or polymeric moiety (2a), and each independently is selected from a bond, (3a)-COO-(2a), (3a)-CONR 2 -(2a), (3a)-O—CO—O-(2a), (3a)-O—CO—NR 2 -(2a), (3a)-NH—CO—NR 2 -(2a), (3a)-O-(2a), (3a)-S-(2a) or (3a)-NR 2 -(2a), wherein (3a) and (2a) indicate the positions of the marker moiety (3a) and the oligomeric or polymeric moiety (2a), respectively; and
(ii) at least one R or R 2 which is not a covalent linking group (4) is not H.

5 . The composition of claim 1 , wherein the moiety (2a) is a resin component or a varnish component.

6 . The composition of claim 1 , which further comprises one or more additional components (6) selected from pigments, dyestuffs, luminescent compounds, oils, resins, solvents, reactive diluents, plasticizers, waxes, fillers, driers, anti-oxidants, surfactants, defoaming agents, catalysts, UV-stabilizers and photoinitiators.

7 . The composition of claim 1 , which is a marked ink.

8 . The composition of claim 7 , which is a staining ink.

9 . The composition of claim 1 , which comprises two or more different marked non-extractable components (5).

10 . An article, comprising a substrate to which a composition (1) of claim 1 and comprising a marked non-extractable component (5) is applied.

11 . The article of claim 10 , wherein the substrate is a banknote or a value document, and the composition (1) is printed on the substrate.

12 . A method for preparing an article comprising applying the composition (1) of claim 1 on a substrate by a printing method, selected from offset, flexographic, gravure, intaglio, inkjet, letterpress, screen printing and combinations thereof, or by a method selected from brushing, roll-coating, spin coating, knife coating, casting, pouring, spraying and combinations thereof.

13 . A method of authenticating a composition (1) of claim 1 present in an article, comprising the steps of
(S 100 ) collecting a sample of the composition (1) from the substrate to obtain a collected sample;
(S 200 ) submitting the collected sample to thermally induced chemical fragmentation conditions to obtain chemical fragmentation products derived from the unit formed of the at least one marker moiety (3a) and the covalent linking group (4) covalently bonded to the oligomeric or polymeric moiety (2a);
(S 300 ) analyzing the chemical products of the chemical sample fragmentation; and
(S 400 ) authenticating the composition (1) by comparing these chemical products to one or more reference substances.

14 . The method of claim 13 , wherein step (S 200 ) comprises pyrolysis of the collected sample at a temperature of 300-600° C., and preferably 450-570° C.

15 . The method of claim 13 , wherein the chemical products of the chemical fragmentation are subjected to (S 210 ) chemical modification during step (S 200 ).

16 . The method of claim 13 , which further comprises a step (S 220 ) of accumulating the marker (3) and/or the chemical products obtained in the chemical fragmentation (S 200 ) and/or modification (S 210 ) in an accumulation means before step (S 300 ).

17 . The method of claim 13 , wherein in step (S 300 ) using gas chromatography (GC) is used for separating different products of the sample fragmentation, and a mass spectrometry (MS) is used for identifying one or more of these products.

18 . The method of claim 17 , wherein a combined pyrolysis-gas chromatography-mass spectrometer, PY-GC-MS, is used to perform the steps (S 200 ) and (S 300 ).

Assignees

• Sicpa Holding Sa

Inventors

• Nouzille Eric
• Demange Raynald
• Degott Pierre

Classifications

• C09D11/03

  characterised by features other than the chemical nature of the binder · CPC title

• B42D25/36

  comprising special materials · CPC title

• B42D25/405

  Marking · CPC title

• Y10T428/24802

  Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] · CPC title

• G07D7/14

  using chemical means · CPC title