GB2136354A - Fingerprinting System - Google Patents
Fingerprinting System Download PDFInfo
- Publication number
- GB2136354A GB2136354A GB08305897A GB8305897A GB2136354A GB 2136354 A GB2136354 A GB 2136354A GB 08305897 A GB08305897 A GB 08305897A GB 8305897 A GB8305897 A GB 8305897A GB 2136354 A GB2136354 A GB 2136354A
- Authority
- GB
- United Kingdom
- Prior art keywords
- impregnated
- card
- pad
- solution
- fingerprint
- 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
Links
- 239000000243 solution Substances 0.000 claims abstract description 53
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims abstract description 24
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000002253 acid Substances 0.000 claims abstract description 9
- 239000007864 aqueous solution Substances 0.000 claims abstract description 8
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000473 propyl gallate Substances 0.000 claims abstract description 6
- 229940075579 propyl gallate Drugs 0.000 claims abstract description 6
- 235000010388 propyl gallate Nutrition 0.000 claims abstract description 6
- 239000005725 8-Hydroxyquinoline Substances 0.000 claims abstract description 5
- 229960003540 oxyquinoline Drugs 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- 239000000758 substrate Substances 0.000 claims description 13
- 239000002904 solvent Substances 0.000 claims description 10
- 238000003384 imaging method Methods 0.000 claims description 9
- 239000011505 plaster Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- 239000003906 humectant Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical group [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 claims description 4
- 229910021578 Iron(III) chloride Inorganic materials 0.000 claims description 3
- 150000001491 aromatic compounds Chemical class 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 235000011187 glycerol Nutrition 0.000 claims description 3
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 3
- 229910052914 metal silicate Inorganic materials 0.000 claims description 3
- VERMEZLHWFHDLK-UHFFFAOYSA-N benzene-1,2,3,4-tetrol Chemical compound OC1=CC=C(O)C(O)=C1O VERMEZLHWFHDLK-UHFFFAOYSA-N 0.000 claims 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 229960002089 ferrous chloride Drugs 0.000 claims 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 239000003599 detergent Substances 0.000 abstract description 7
- 238000004140 cleaning Methods 0.000 abstract description 6
- 239000004744 fabric Substances 0.000 abstract description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000004033 plastic Substances 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical class OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000000976 ink Substances 0.000 description 6
- 239000011148 porous material Substances 0.000 description 5
- -1 alkylene glycol Chemical compound 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000004922 lacquer Substances 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- BRRSNXCXLSVPFC-UHFFFAOYSA-N 2,3,4-Trihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1O BRRSNXCXLSVPFC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000011928 denatured alcohol Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 229940096992 potassium oleate Drugs 0.000 description 2
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 239000004699 Ultra-high molecular weight polyethylene Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- JBTHDAVBDKKSRW-UHFFFAOYSA-N chembl1552233 Chemical compound CC1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 JBTHDAVBDKKSRW-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- WUUZKBJEUBFVMV-UHFFFAOYSA-N copper molybdenum Chemical compound [Cu].[Mo] WUUZKBJEUBFVMV-UHFFFAOYSA-N 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002984 plastic foam Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 150000004322 quinolinols Chemical class 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000005437 stratosphere Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/117—Identification of persons
- A61B5/1171—Identification of persons based on the shapes or appearances of their bodies or parts thereof
- A61B5/1172—Identification of persons based on the shapes or appearances of their bodies or parts thereof using fingerprinting
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medical Informatics (AREA)
- Biophysics (AREA)
- Pathology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
Abstract
Fingerprints images are formed by applying the distal portion 29 of a finger 32 to a porous pad 10 impregnated with a solution of marking compound. The finger portion may be prewetted or cleaned with cloth 30 impregnated with detergent solution. The finger 32 is then applied to a square 36 of a fingerprint card 38 impregnated with a developer for the marking compound e.g. an aqueous solution of polyhydroxy developer such as 8-hydroxy-quinoline and propyl gallate containing a high molecular weight dibasic acid such as azelaic acid. A fingerprint image 40 immediately develops. Traces of the image can be removed with a cleaning solution impregnated cloth 42. <IMAGE>
Description
SPECIFICATION
Improved Fingerprinting System
Technical Field
The present inventions relate to an inkless fingerprint identification system and, more particularly, to a system and method for directly imaging fingerprints on a fingerprint card without the need for application of a fluid developer.
Since fingerprint patterns of ridge endings and ridge bifurcations do not vary with time for an individual and the pattern on each finger for any individual is unique and differentiates that individual from the rest of the society, fingerprint comparison is an absolute means of identification.
This fact has been accepted by the scientific community and by the courts. Fingerprint identification is legally recognized forensic evidence of an individual's presence at a scene or assocation with property or instruments used in a crime. Fingerprint identification is also used commercially such as on identification cards for security systems, check identification means, and in many non-criminal government agencies.
Any reliable fingerprint identification system requires imaging a distinct print pattern on a substrate. Even in commercial identification systems such as with checks, it is important that the system be inoffensive to the subject. The early inking systems were difficult to utilize since it required much skill, training and care to provide a distinct print without ink running between ridges and obliterating substantial areas of the print image. Furthermore, the inking system was messy to use to both the operator and the subject requiring towelettes or a trip to a wash basin in order to remove the ink.
There have been several different inkless fingerprint systems proposed such as magnetisable powder system disclosed in U.S.
Patent No. 3,831,552 or various imaging systems based on reaction between metal salts and polyhydroxy aromatic compounds. One very convenient implementation of this imaging reaction as an inkless fingerprinting system is the impregnation of a pad with one of the metal salts such as an iron chloride.
After the subject applies the distal surface of his finger against the pad to form a thin coating of the metal salt the finger is then pressed against the substrate such as a check or fingerprint card with a rolling motion. The substantially invisible fingerprint is then developed in a developer appartus having a tray for receiving the card and an aerosol, pressurized container for dispersing a spray of developer onto the invisible fingerprint pattern.
The metallic salt on the card and the spray applied organic developing compound quickly react to form a colored compound which renders the fingerprint visible to form a permanent record.
However, due to the belief that the accumulation of fluorocarbons in the stratosphere will deplete the ozone layer and cause excessive ultraviolet radiation on the surface of the earth, the U.S.
Government has restricted and in some cases eliminated the use of fluorocarbons as a propellant.
Disclosure of the Invention
An improved fingerprinting identification system is provided in accordance with the present invention. This system eliminates the use of propellants for any nature and does not require the spray application of developer. The system of the invention provides a dark, distinct fingerprint image as a permanent record of a substrate in a simple, efficient and reliable manner and uses techniques and materials familiar to operators of fingerprinting systems. The fingerprint image in the present invention develops rapidly and distinctly and forms a permanent record for use in any of the security or forensic procedures previously practiced in the fingerprinting field.
In accordance with the present invention, the chemical developer previously applied by spray is directely impregnated into the porous substrate.
Therefore, on transfer of the metal salt pattern to the impregnated substrate a print of the finger ridge pattern will develop. There have been other attempts to develop a developer impregnated or coated card system such as U.S. Patent 2,082,735. However, that patent requires that the trihydroxybenzoic acid be applied to the card as a coating, in a lacquer or other vehicle such as a glue-pigment composition. Lacquer coatings are not suitable for pre-printed cards because the solvent will dissolve the pre-inked matter such as the matrix of boxes for receiving the individual fingerprint impressions. Furthermore, a cured lacquer will ride on top of the surface as a shiny skin film which may tear or separate from the surface.Furthermore, the lacquer encapsulates the developer and renders unavailable# some of the ink compound within the cured interior portion of the coating, leaving only the surface trihydroxybenzene compounds available for marking reaction with-the metal salt.
It was therefore decided to attempt to prepare a card treated such that the marking compound would be impregnated into a surface layer or throughout the body of-the card. In this manner, either uncoated or pre-inked stock could be used to form the dry-imaging fingerprint card of the invention. However, in early attempts to utilize such cards it was found that the cards worked well when fresh in that an image would develop very quickly or "pop up" so as to be visible within a short time after application of the metal salt carrying fingerprint to the card. However, if these cards were allowed to sit for a few days or a few weeks, the image would only slowly develop over a very long period of time.After much experimentation of the various additives to control penetration viscosity and marking ability, it was found that the addition to the impregnant of a high molecular weight dibasic acid containing at least six carbon atoms, suitably azelaic acid provides an impregnating composition that results in a treated fingerprint card that gives
instant imaging to form a distinct, very dark
fingerprint image.
Another, unexpected result was the discovery
that relatively low concentrations of azelaic acid,
typically 2 to 5 percent by weight, were effective in
adapting the solvent solution to be used as a
printing "ink" or fluid. This feature is of special
important as it provides a fast, simple and
economical means of coating, impregnating or
imprinting cards of a variety of sizes with the
tryhydroxybenzene solution being deposited only in
certain sharply defined areas, such as for example
the rectangular section of a fingerpring card
described by the points A-B-C-D in Figure 3.
Other aspects of the invention relate to an
improved pad composition in which the sawdust
ingredient utilized in Patent No. 3,960,632 is
replaced with a very finely divided silicate
material. Another aspect of the invention relates
to the discovery that application of a detergent composition to the distal portions of the fingertips
before application of the fingers to the pad
containing the metal salt results in much darker,
immediate imaging when the fingerprint patterns
are transferred to the impregnated card.
These and many other objects in attendant
advantages of the invention will become apparent
as the invention becomes better understood by
reference to the following detailed description
when considered in conjunction with the
accompanying drawings.
Brief Description of the Drawings
Figure 1 is in a perspective view of the finger
print marking solution impregnated pad from the
invention;
Figure 2 is a sectional view taken along the line 2-2 of figure 1;
Figure 3 is a front elevational view of a
fingerprint card treated in accordance with the
invention;
Figure 4 is a sectional view taken along the line 4-4 of figure 3;
Figures 5A, B, C, D and E are schematic views
of the steps utilized in preparing a fingerprint
record in the system of the invention.
Referring now to figures 1 and 2, the applicator
1 0 for applying the solution of fingerprinting
marking compound to a finger comprises a
container 12 receiving a porous matrix 14
impregnated with marking solution A reservoir of
solution may be provided by disposing a porous
resilient member 16 such as a felt disc in the
bottom of the container.
The propous pad member 14 is preferably fairly
rigid so that only the ridges of the distal ends of
the finger are wetted and moistened by the
marking solution. The pad is formed of a material
that is inert to the marking solution, either an
inorganic material such as plaster or a porous
plastic such as the UHMWPE plastic sheeting
produced by The Porex Division of Glasrock
(Fairburn, Georgia) or the Porelon plastic parts
produced by The Porelon Inc. subsidiary of
Johnson Way (Cookeville, Tennessee).
While both porous plaster and porous plastic pads have been found to work in accordance with the concept of this invention, the size of the microscopic pores have been observed to determine the sharpness, clarity or resolution of the resultant fingerprint image. Macroporous plastic pads, for example, which have pore openings or cells greater than 10 microns in diameter, produce a coarse fingerprint image wherein the cell structure is apparent and some detail is lost.
Microporous plastics and plaster pads molded in accordance with the present invention, have a much finer pore structure with openings less than 10 microns in diameter. These produce the clearest, sharpest prints in which every detail of the fingerprint ridge is preserved and no overall pore pattern is discernible.
A high porosity pad is formed by adding 1 to 10% of a finely divided silica, or a finly divided metal silicate absorbant such as diatomaceous earth to a white plaster formulation. The porous pad composition may also contain 0.1 to 2% of a coloring agent such as a red oxide dye. The dry ingredients are dispersed in about 100 to 500milliliters of tap water on a dry basis. A suitable example of practice follows:
EXAMPLE 1
10 ounces of tap water are placed into a onequart blender container and the blender turned on at low speed. 0.8 grams of Oxide Red No. 103 and 5 grams of HiSil T-600 silica are then added and blended at high speed for a minute. This red liquid is poured into a two-quart mixing bowl and 514 grams of white plaster is added slowly into the mixing bowl and stirred for two minutes.After the mixture has deaerated for one minute it is remixed for a minute and then poured into a suitable mold cavity on a vibrating table and vibrated for 15 to 20 seconds. The vibrator is then turned "off" and the felt pad is placed on the top of the mold. The pad is allowed to cure for about35 minutes and then removed from the mold. The pad may be subjected to a final heat cure at a temperature of about 80-1 500F for a period of about 2-20 hours under moderate air flow. The dried pad is then removed from the mold and placed in a container 12 in the inverted position with the felt layer 16 at the bottom. The pad 10 is now ready for impregnation with marking solution. The pad is totally immersed in the solution and should be soaked into the pad for a period of at least five days, preferably at least two weeks even though it appears to penetrate earlier.
The pad soaking solution comprises a solution of a water-soluble metal salt marking compound and a water soluble humectant. The solution may also contain a small amount of a wetting agent or detergent. The solution generally contains, on a relative basis, 20 to 100 parts by weight of humectant; 2 to 30 parts by weight of metal salt; and optionally 0 to 100 parts of water. A small amount of detergent such as 1 to 10 grams of
Aerosol OT (75% AQ) may be added. The ingredients are mixed to form a clear solution which is then soaked into the pad and allowed to penetrate for at least 24 hours preferably at least 5 days as discussed. The solution enters the cells of the porous plaster matrix and the remainder is stored in the felt pad reservoir. The pad may be regenerated by resoaking after many hours of service.The pad can be formed of other materials such as rigid plastic foams and the like.
The soluble metal salt reactive with the hydroxyphenolic compound can be a metal from groups I to VIII of the periodic table and the anion may be inorganic such as halide, sulfate or ferrocyanide. A preferred marking ingredient, due to cost, availability, nontoxicity and safety, is ferric chloride. Ferric chloride may be used in a mixture with 5 to 30% of its weight of ferrous chíoride.
The solvent for the salt is preferably a liquid that does not evaporate under ambient conditions and also preferably as a humectant in order to keep the pad from drying out under normal conditions.
Preferred solvent-humectahts are materials such as glycerine, an alkylene glycol such as ethylene glycol or propylene glycol or various low molecular weight polyether liquids based on ethylene and/or propylene oxide; A suitable example of a pad soaking solution follows:
EXAMPLE 2
Material Amount
Glycerine 23,866 grams
FeCI3 6H20 5,818 grams FOCI, ~ 4H2O 763 grams
Aerosol OT 8m1 Referring now to figures 3 and 4, the hydroxyaromatic compound that forms the marking reaction with the metal salt is impregnated into a substrate, suitably a fibrous substrate such as a paper check or ID card 20, by impregnation from solution.The card 20 will have a data receiving area 22 on the top portion thereof and a fingerprint matrix receiving portion 24 in the lower half thereof, bounded by points A-B-C-D.
The marking solution need only be impregnated into the fingerprint portion 24 of the card.
The metal salt is preferably a salt of a transition metal such as iron, titanium, vanadium, chromium, magnesium, cobalt, nickel, copper molybdenum, tungsten and the like with an anion such as ferride, citrate, sulfate, nitrate, stearate, acetate, formate, phosphate and the like.
The preferred marking ingredients are quinolinol derivatives, preferably 8-hydroxyquinoline and various substitute derivatives thereof alone or in combination with a polyhydroxy phenol compound, such as trihydroxy benzoic acid, pyrogallol, catechol, gallic acid, propyl gallate, and the like. The marking reaction should be such as to give a clear and distinct image, preferably a very dark, black colored image. The impregnating composition is formed as a solution in a common solvent. Solvents such as acetone are utilizable, however, for inhalation reasons and due to the tendency of acetone to dissolve preprinted areas of the fingerprint card, it is preferred to utilize an alcohol solvent, suitably a lower alkanol such as methanol, ethanol or mixtures thereof.The marking composition contains, based on 100 grams of solvent, 10 to 40 parts by weight of marking compound, and 1 to 10 parts of the high molecular weight dibasic/acid additive of the invention. The composition may also contain from 0.1 to 3 parts of a finely divided silica as a thickener. The preferred composition contains a mixture of a trihydroxybenzene such as propyl galla#te# and 8-hydroxyquinoline in a ratio of at least five to one of the gallate to the hydroxy-quinoline, preferably at least ten to one. The preferred dibasic acid is azelaic acid. A card impregnating solution is made by heating the solvent gently with stirring to dissolve ingredients while maintaining a maximum temperature of 450 until the azelaic acid is dissolved, then removing the heat and adding the finely divided silica such as Cab-0-Sil, if desired.
A suitable example of practice follows.
EXAMPLE 3
Material Amount
Denatured alcohol 1540 Ml Propyl Gallate 240 grams 8-Hydroxy-Quinoíine 1 5;75 grams
Azelaic Acid 60 grams
Cab-O-Sil M5 7.5 grams
The cards are coated with this solution or preferably imprinted by means of the water fountain of an offset press on a basis of 0.01 to
10 pounds of impregnating solution for 3,000 square feet of cards. It has been determined that for normal~ cards and good imaging, the coating basis can generally be 0.5 to 1.0 pounds per 3,000 square feet of cards.
Many different dibasic fatty acids and fatty acid salts were investigated since impregnated cards, after aging for several weeks did not "pop up" (produce an image instantly) when the fingertip wetted with iron chloride solution was applied to them. A standard solution based on 205 (ml) by weight of denatured alcohol and 32 grams propyl gallate to 2.1 grams of 8-hydroxyquinoline was prepared. To each of these solutions was added 8 grams by weight of either stearic acid, palmitic acid, azelaic acid, or potassium oleate. All of these solutions, including a control solution without any additive, were coated onto standard FBI fingerprint cards. The card impregnated with the solution containing azelaic acid gave the darkest print.
Potassium oleate also gave a dark image but the solution appeared to be unstable. The control image popped up when cards were freshly coated but developed slowly with cards that had been stored for several weeks. Impregnating solution for the card treated with the solution containing azelaic acid, when further modified to include 1 gram of Cab-O-Sil M5 (finely divided silica), gave a further improved fingerprint definition.
While the exact mechanism is unknown, by which fresh cards pop up and aged cards produce a fingerprint image that develops slowly, it is likely that the trihydroxybenzene, or other polyhydroxyphenolic compounds used, with time, gradually diffuse away from the surface into the body of the card stock making them less available for instant reaction.
Azelaic acid and other dibasic fatty acids that are soluble in the card coating solution appear to enhance or intensify the image, to serve as a carrier for the polyhydroxy phenolic reagents used, and to act as a filler or blocking agent. In this last role, the dibasic acid could conceivably fill the pores or interstices of the fingerprint card or other fibrous substrate, thereby preventing the reagent solution from diffusing away from the card surface.
Thus, the high molecular weight, dibasic acids of this invention appear to serve at least four unique functions: First, they act as an intensifier to increase the density of the fingerprint image; second, they serve as fillers or carriers to hold the color forming reagents at the fingerprint card surface keeping them available for instant reaction; third, they function as viscosity builders, solution thickeners, or tackifying agents to enable the reagent solution to assume the properties of a fluid ink, capable of being imprinted in welldefined areas by means of a printing process such as offset lithography; and, fourth, they prevent the freshly formed fingerprint from feathering, bleeding or blotting as the moist image is prone to do by virtue of the wicking action of paper fibers.
This feathering problem has been a particular drawback with prior art inkless fingerprint solutions.
It was further discovered during the development of the invention that the darkness of the immediate fingerprint varied from time to time and with different operators. After investigation it was discovered that this usually cccured when the surface of the pad was dry. This can be remedied by rewetting the pad with salt solution or, more conveniently and reliably, by prewetting the fingers with an aqueous solution of detergent prior to fingerprinting resulted in significant image enhancement. A convenient form of practicing such a step would be to impregnate the detergent solution onto a fibrous substrate such as paper or cloth.It is not known whether the image enhancement is a result of the wetting agent of the simple fact of pre-moistening of the finger before application to the pad or of the removal of natural oils from the skin surface which would repel the pad solution and therefore prevent application of a uniform layer on the finger. A suitable solution for use in impregnating the fibrous substrate would contain an aqueous solution of a suitable surfactant such as Triton X100 or Aerosol OT. An example of a suitable solution follows:
EXAMPLE 4
Material Amount
Triton-x 100 1-2 grams 10-1 5 less 1% Isopropyl alcohol
remainder preservatives and
buffer water
The process of the invention is an inkless system in terms of avoiding handling greasy
conventional inks.However, the repeated use of the system within a short period of time may
result in staining of the fingertips of the user or
operator. It is therefore desirable to provide a cleaning solution to remove the stains. The cleaning solution may contain an organic solvent for the marking compound such as a non
hazardous alcohol suitably methanol, ethanol or
propanol and a soluble metal chelating agent such as citric acid. The solution may also contain a surfactant. Again the cleaning solution can be conveniently impregnated into a fibrous substrate such as paper or cloth and can be cut into small pieces such as found in commercial hand wiping products.An example of a suitable solution follows:
EXAMPLE 5
Material Amount
Distilled water 500 Ml
2-Propanol 400 MI
Citric acid 130 grams Aerosol OT 2 MI
We have found that the impregnated paper product previously described to pre-wet the fingers before use of the system may be utilized as the cleaning solution after use of the system if it is formulated to contain a marking compound solvent such as propanol.
Referring now to Figures 5A to 5E, the system of the invention may be provided in a kit form such that all parts may be integrated and used together in a cooperative mode. In a description of the complete use of the system, the distal portion 29 of a finger 32 is pre-wetted with a detergent solution impregnated into cloth 30. The wetted finger 32 is then applied to the top surface 34 of a marking compound impregnated, porous plaster or porous plastic pad 10. The finger of the subject 32 containing an invisible pattern of marking compound, is then applied to a correlated square 36 of a developer impregnated fingerprint card 38. A fingerprint pattern 40 immediately develops. The finger 32 of the user is then cleansed with a cleaning solution impregnated pad 42.
It is to be realized that only preferred embodiments of the invention have been described and that numerous substitutions, alterations and modifications are all permissible without departing from the spirit and scope of the invention as defined in the following claims.
Claims (21)
1. A method of producing a print of a finger or other body part comprising the steps of:
applying a .marking compound to said part to form an image;
transferring said image to a card impregnated with a developer for said marking compound and forming a dark image on said card.
2. A method according to Claim 1 in which said marking compound is a water soluble metal salt and the developer comprises a polyhydroxy aromatic compound.
3. A method according to claim 2, in which the metal salt is dissolved in an aqueous solution impregnated into a porous pad and said solution also contains a humectant.
4. A method according to claim 3, in which the pad is a porous plaster containing a finely divided silica or metal silicate.
5. A method according to claim 4, in which the metal salt is an iron chloride.
6. A method according to claim 5, in which the chloride is a mixture of ferrous chloride and ferric chloride.
7. A method according to claim 3, in which an aqueous solution is applied to the part before application of the part to the pad.
8. A method according to claim 7 in which the aqueous solution is impregnated into a fibrous substrate.
9. A method according to Claim 8 further including the step of removing any developed image from said body part by wiping the body part with a fibrous substrate impregnated with a solvent for the developed image.
10. A method according to Claim 2 in which the card is impregnated only in the fingerprint receiving area thereof.
1 1. A method according to Claim 10 in which the impregnant comprises an aqueous solution containing a dibasic organic acid containing at least 6 carbon atoms.
12. A method according to Claim 1 1 in which the marking compound comprises a mixture of a quinolinol and a trihydroxy phenol.
13. A method according to Claim 12 which the acid is azelaic acid and the mixture comprises 82 hydroxyquinoline and propyl gal late.
14. A pad for applying a marking compound to a finger or other body part comprising 1 to 10% by weight of a porous plaster pad containing a finely divided silica or metal silicate impregnated with a solution of water soluble marking compound and a humectant.
15. A pad according to Claim 14 in which the compound is iron chloride and the humectant is glycerine.
16. A fingerprint imaging device comprising:
a card having a first information receiving area and a second fingerprint receiving area;
at least said second area being impregnated with an aqueous solution of a polyhydroxy developing marking compound containing 2.to 5 percent by weight of a water soluble dibasic fatty acid containing at least 6 carbon atoms.
17. A card according to Claim 16 in which only said second area is impregnated.
18. A card according to Claim 17 in which the marking compound is a mixture of a quinolinol and a trihydroxy aromatic compound.
19. A card according to Claim 18 in which the mixture comprises 8-hydroxy-quinoline and propyl gal late.
20. A card according to Claim 19 in which the dibasic acid contains 8 to 18 carbon atoms.
21. A card according to Claim 20 in-which the dibasic acid is azelaic acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB08305897A GB2136354B (en) | 1983-03-03 | 1983-03-03 | Fingerprinting system |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB08305897A GB2136354B (en) | 1983-03-03 | 1983-03-03 | Fingerprinting system |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB8305897D0 GB8305897D0 (en) | 1983-04-07 |
| GB2136354A true GB2136354A (en) | 1984-09-19 |
| GB2136354B GB2136354B (en) | 1986-05-29 |
Family
ID=10538933
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB08305897A Expired GB2136354B (en) | 1983-03-03 | 1983-03-03 | Fingerprinting system |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2136354B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0296121A3 (en) * | 1987-06-15 | 1990-05-30 | Lipatec Etablissement | Individual distributor of reactive liquid for fingerprints |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB414840A (en) * | 1933-04-18 | 1934-08-16 | Charles Frederick Thackray | A new or improved method or process of taking foot impressions, and a chart or pad device for use in connection therewith |
| GB428386A (en) * | 1933-11-13 | 1935-05-13 | William Heinecke | Improved method of producing visible finger or like imprints |
| GB852919A (en) * | 1957-07-15 | 1960-11-02 | Reed Kenneth J | Improvements in or relating to the production of finger print impressions |
| GB1534746A (en) * | 1975-12-18 | 1978-12-06 | Identicator Corp | Two part inkless applicator for fingerprints and method of retaining fingerprints |
-
1983
- 1983-03-03 GB GB08305897A patent/GB2136354B/en not_active Expired
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB414840A (en) * | 1933-04-18 | 1934-08-16 | Charles Frederick Thackray | A new or improved method or process of taking foot impressions, and a chart or pad device for use in connection therewith |
| GB428386A (en) * | 1933-11-13 | 1935-05-13 | William Heinecke | Improved method of producing visible finger or like imprints |
| GB852919A (en) * | 1957-07-15 | 1960-11-02 | Reed Kenneth J | Improvements in or relating to the production of finger print impressions |
| GB1534746A (en) * | 1975-12-18 | 1978-12-06 | Identicator Corp | Two part inkless applicator for fingerprints and method of retaining fingerprints |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0296121A3 (en) * | 1987-06-15 | 1990-05-30 | Lipatec Etablissement | Individual distributor of reactive liquid for fingerprints |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2136354B (en) | 1986-05-29 |
| GB8305897D0 (en) | 1983-04-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19930303 |