US2986831A - Process for lifting skin imprints - Google Patents
Process for lifting skin imprints Download PDFInfo
- Publication number
- US2986831A US2986831A US760071A US76007158A US2986831A US 2986831 A US2986831 A US 2986831A US 760071 A US760071 A US 760071A US 76007158 A US76007158 A US 76007158A US 2986831 A US2986831 A US 2986831A
- Authority
- US
- United States
- Prior art keywords
- film
- polymer
- liquid
- skin
- imprint
- 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.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 17
- 239000007788 liquid Substances 0.000 claims description 34
- 229920000642 polymer Polymers 0.000 claims description 30
- 239000000843 powder Substances 0.000 claims description 15
- 239000007787 solid Substances 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 13
- 239000011248 coating agent Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 238000010410 dusting Methods 0.000 claims description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 24
- 239000002904 solvent Substances 0.000 description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000428 dust Substances 0.000 description 8
- 229940073584 methylene chloride Drugs 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 239000004952 Polyamide Substances 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- 239000003380 propellant Substances 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000000443 aerosol Substances 0.000 description 4
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000008199 coating composition Substances 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 239000002390 adhesive tape Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 3
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 229940042935 dichlorodifluoromethane Drugs 0.000 description 2
- 229920002681 hypalon Polymers 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N methyl pentane Natural products CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical class FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical group CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical class CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004348 Glyceryl diacetate Substances 0.000 description 1
- 240000002636 Manilkara bidentata Species 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000016302 balata Nutrition 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- WGLUMOCWFMKWIL-UHFFFAOYSA-N dichloromethane;methanol Chemical compound OC.ClCCl WGLUMOCWFMKWIL-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 210000000416 exudates and transudate Anatomy 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 235000019443 glyceryl diacetate Nutrition 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- -1 magnesium oxide Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- KSCKTBJJRVPGKM-UHFFFAOYSA-N octan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-] KSCKTBJJRVPGKM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 229920000260 silastic Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C39/00—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor
- B29C39/02—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor for making articles of definite length, i.e. discrete articles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
Definitions
- This invention relates to a new process for lifting latent skin imprints from surfaces on which they are found.
- the object of this invention is to provide a method for lifting dusted skin prints from surfaces .of substantially any type, shape or size, while retaining the original clarity and definition of the dust-developed print.
- Another object is to provide a means for lifting dusted latent prints which, per se, forms a clearly readable, permanent, readily fileable record.
- the finely divided powder used for dusting the latent skin print can be any material conventionally used for the purpose, such as powdered graphite, charcoal, lampblack, aluminum or other powdered metal, boron nitride,
- the powder can be chosen to provide a contrasting color with the film.
- the powder is dusted on the surface bearing the latent skin print and the nonclinging excess removed in conventional fashion to develop the print, namely a print showing the characteristic pattern of the skin visibly outlined by the dust.
- the liquid coating composition essentially comprises a natural or synthetic polymer settable into a solid, flexible, strippable film which is also preferably non-tacky.
- the hardened film must not adhere so tenaciously to the surface to which it is applied that it cannot be readily re moved or stripped. Flexibility is important so that it can be removed and manipulated without breaking or tearing. Substantial freedom from tackiness is also desirable since this improves its handling and filing characteristics.
- Still another object is to provide a process for lifting dusted skin prints which is simple, easy to apply by anystrippable, flexible, preferably non-tacky, film, and then stripping the hardened film from the surface.
- the liquid coating flows over and conforms to the contours of the dusted print pattern without disturbing it.
- a finely-divided powder such as talc or a conditioning agent which does not obscure the embedded print pattern.
- a finely-divided powder such as talc or a conditioning agent which does not obscure the embedded print pattern.
- a finely-divided powder such as talc or a conditioning agent which does not obscure the embedded print pattern.
- Polymers and copolymers having the desired characteristics per se or by modification with such components as plasticizers to improve flexibility and strength, tackiness inhibitors such as finely divided inorganic mate rials which are insoluble in the fluid composition, e.g. magnesium oxide and other metal oxides, talc, silica and carbon black, and the like, are well known to those skilled in the art.
- the liquid coating compositions can also advantageously be colored by incorporation of a suitable dye or finely divided pigment so as to provide a'marked contrast with the dust employed to develop the latent print, thereby increasing clarity and readability of the embedded print.
- the liquid coating is preferably a fluid solution of a solid polymer dissolved in a volatile solvent, in which case setting of the applied coating can be rapidly achieved by evaporation of the solvent upon exposure of the large film surface to air.
- Such polymer solutions have the practical advantages of being preparable in the final form of use long in advance, of being packageable in a single container, and of requiring no further treatment to produce hardening.
- Films can be made from polymer solutions containing volatile solvents, which harden within a matter of minutes, in some cases as little as a minute or two. If desired, of course,-evaporation of the solvent and consequent hardening of the film can be speeded up by warming, but ordinarily this is not necessary.
- Any natural or synthetic solid polymer can be employed forour purpose, which can be dissolved in a volatile solvent to form a fluid solution and which, after evaporation .of the solvent forms a strippable, flexible, preferably'non-tacky film, either iperse or by modification with conditioningv components, such. .as plasticizers dispersed tackiness inhibitors, and the like.
- polyamides which are soluble in volatile solvents at ordinary temperatures, such as theN-alkoxyalkyl polyamide derivatives; acrylic and methacrylicresins and their, copolymers, such as polyacrylamide, polymerized unsaturated hydrocarbon and halogenated hydrocarbon;
- cosolvent systems such asv methylene chloride-methanol, chloroform methanol, ethanol-water, can be used for such reasons as improved solubility and reduced viscosity.
- the concentration of the dissolved polymer is not critical and is dictated only by such practical considerations asthe thickness of-film desired, the optium setting time for particular applications and the viscosity of the solution; About 5 to solutions areusually ade-:
- plasticizers which "can be employed include dibutyl and dioctylphthalate,.dibutyl and diethyl sebacate, trioctyl, triphenyland tricresylphosphate, butyl stearate, diacetin, high molecular weight alcohols, such as octanol, decanol, and the like.
- conditioners such as tackiness inhibitors
- tackiness inhibitors can also be dispersed in the polymer solution. In general, this will not be necessary,since-suitable polymers which form non-tacky films can readily be selected.
- Polymerizable liquids which can be. cured into a solid, strippable, flexible film after application to a surface can 4 a o a. p r ly redli uid n ym rts sh.ass ttaian ta.
- the liquid coatings can be applied to the surface bearing the dusted skin prints in any suitable and convenientmanner, although care should be taken not to apply it, in so forceful a manner as to disturb the dusted printas, V for example, by hard brushing.
- the liquid can be flowed. on as, for example, by dropping small amounts on the sur face and permitting it to flow into a film.
- the most convenient mode of application is by spray-- ing, which can be accomplished in any desired manner.
- the solution can be sprayed from a manually operated container or from one pressurized by an inert gas such as nitrogen or carbon dioxide. It can also, in some cases, v be sprayed as an aerosol, Where the particular polymer solution is miscible with a propellant agent maintained in the liquid state at normal temperatures by the application of pressure.
- Such propellant agents include, for example, methyl'chloride and various chlorofluoro methanes and ethanes, such as dichlorodifiuoromethane (Freon-12), monochlorodifluoromethane (Freon-22), and dichlorotetrafiuoroethane (Freon-114)
- dichlorodifiuoromethane Freon-12
- monochlorodifluoromethane Freon-22
- dichlorotetrafiuoroethane Freon-114
- Table I summarizes other film-forming polymer solutions which we have prepared and found suitable for our also be'employed.
- the curing agent can be beat applied purpose.
- Table l Polymer Concen- Solvent Other additives tratlon a Polyisobutylene 2 Do 10 1% o Polyisobutylene 2 I Mlerocrystalllne wax 10 phr.
- Tacklness inhibitor 1 Plastieizer to improve flexibility.
- Cocoon 560 and Cocoon 501 solutions of vinyl chlo' ride-vinyl acetate copolymer in methyl ethyl ketone.
- Hysol 6101-B a solution of a partially cured epoxy resin which drys to form a non-tacky film.
- EXAMPLE III A solution of N-methoxymethyl polyamide was prepared by dissolving 10 grams of the polymer in 100 ml. methanol/methylene chloride, 60/40. The solution was loaded into an aerosol container and pressurized with dichlorodifluoromethane (Freonl2) in a ratio of 50 parts polymer solution to 40 parts propellant liquid. The aerosol mixture was readily sprayed, forming films from 2 to 4 mls. in thickness with two passes of spray. The films were tack-free in less than 2 minutes and could be stripped in less than 10 minutes. The lifted imprints were clear and sharp.
- Reonl2 dichlorodifluoromethane
- EXAMPLE IV A commercially available aerosol solution of a polyacrylamide (Krylon #1301) produced satisfactory films when given a drying time of one-half hour after each pass.
- the resulting films were flexible, non-tacky and strippable.
- a process for lifting a latent skin imprint from a non-skin surface which comprises developing said imprint by dusting with a finely divided powder, coating the surface carrying the dusted imprint with a liquid composition consisting essentially of a polymer settable into a solid flexible, substantially non-tacky, strippable film, said dusting powder being insoluble in said liquid composition, setting the coating into a solid film, and separating the" film from said surface, said stripped film carrying embedded therein the finely divided powder in the pattern of said skin imprint.
- a process for lifting a latent skin imprint from a non-skin surface which comprises developing said imprint by dusting with a finely divided powder, coating the surface carrying the dusted imprint with a liquid composition consisting essentially of a solution of a solid polymer dissolved in a volatile solvent, said liquid coating, upon evaporation of the volatile solvent, forming a solid, flexible, substantially non-tacky, strippable film, said dusting powder being insoluble in said liquid composition, permitting said coating to set into a solid film, and separating the film from said surface, said stripped film carrying embedded therein the finely divided powder in the pattern of said skin imprint.
- liquid coating composition is a solution of a polyamide which is soluble in a volatile solvent at ordinary temperatures.
- liquid coating composition is a solution of an N-alkoxyalkyl polyamide in a mixture of methylene chloride and methanol.
- N-alkoxyalkyl substituent is N-methoxymethyl and the ratio of methylene chloride to methanol is from about 40:60 to :35.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Medicinal Preparation (AREA)
Description
Unite This invention relates to a new process for lifting latent skin imprints from surfaces on which they are found.
It is frequently necessary to identify latent skin prints, present on furniture, walls, utensils, paper and other surfaces, for criminal and other detection purposes. Such prints are usually developed or made more clearly visible by dusting with a finely-divided powder which clings to the oils and other body exudates impressed in a characteristic pattern onto the surface by contact with the skin of the fingers, palm or foot.
Identification of the developed prints generally requires comparison with prints recorded in official files. To make this posa'sible, it is usually necessary to make an accurate duplicate of the dusted print on an easily carried, fileable surface. This has hitherto been done by photographing the dusted print or by lifting it from its surface site by applying to it an adhesive tape which, upon withdrawal, removes the dust from the surface in the characteristic pattern of the skin print. Photography fails where the surface is inaccessible to the camera or is so curved as to produce distortion in the picture. Lifting by adhesive tape can be employed in such situations but has certain undesirable features. Pressure must be applied to the tape to ensure its adherence to the surface and the dust. Such application of pressure tends to spread the dust which, while clinging to the latent print, is not tenaciously held to the surface. To lift the print in its original definition, it is also necessary to apply pressure on the adhesive tape uniformly over the entire area. This is often diflicult to do particularly if the surface is curved. As a result the dust pattern picked up on the tape is usually difiused and fuzzy. The prepared tape is generally obtainable only in sheets or strips of limited width so that where a large surface area is to be covered, as, for example, in the case of a large hand print, the tape must be applied in sections with resulting distortion. Although no difficulty is ordinarily experienced with cylindrical curved surfaces, some distorting wrinkling occurs when the flat, non-elastic tape is applied to substantially spherical surfaces. The sticky tape, furthermore cannot be easily handled or filed so that it must either be covered with a non-tacky transparent liner or photographed.
The object of this invention is to provide a method for lifting dusted skin prints from surfaces .of substantially any type, shape or size, while retaining the original clarity and definition of the dust-developed print.
Another object is to provide a means for lifting dusted latent prints which, per se, forms a clearly readable, permanent, readily fileable record.
ate t 2,986,831 Patented June 6, 1961 faces. It is, furthermore, easy to store, carry and use,
being appliable from a container by any suitable means as, for example, by spraying or by dropping a small amount on the surface and allowing the liquid to spread into a film.
The finely divided powder used for dusting the latent skin print can be any material conventionally used for the purpose, such as powdered graphite, charcoal, lampblack, aluminum or other powdered metal, boron nitride,
metal oxides such as magnesium oxide, flour, talc, and the like, which is not soluble in the subsequently applied liquid coating. The powder can be chosen to provide a contrasting color with the film. The powder is dusted on the surface bearing the latent skin print and the nonclinging excess removed in conventional fashion to develop the print, namely a print showing the characteristic pattern of the skin visibly outlined by the dust.
The liquid coating composition essentially comprises a natural or synthetic polymer settable into a solid, flexible, strippable film which is also preferably non-tacky. The hardened film must not adhere so tenaciously to the surface to which it is applied that it cannot be readily re moved or stripped. Flexibility is important so that it can be removed and manipulated without breaking or tearing. Substantial freedom from tackiness is also desirable since this improves its handling and filing characteristics. Although desirable, it is not essential that the set film itself be completely non-tacky, since tackiness of the formed film, in many cases can be eliminated by light dusting Still another object is to provide a process for lifting dusted skin prints which is simple, easy to apply by anystrippable, flexible, preferably non-tacky, film, and then stripping the hardened film from the surface. The liquid coating flows over and conforms to the contours of the dusted print pattern without disturbing it. When the coating sets into a solid film, the dust, in the characteristic pattern of the print, is firmly embedded therein,
with a finely-divided powder, such as talc or a conditioning agent which does not obscure the embedded print pattern. Polymers and copolymers having the desired characteristics per se or by modification with such components as plasticizers to improve flexibility and strength, tackiness inhibitors such as finely divided inorganic mate rials which are insoluble in the fluid composition, e.g. magnesium oxide and other metal oxides, talc, silica and carbon black, and the like, are well known to those skilled in the art.
"The liquid coating compositions can also advantageously be colored by incorporation of a suitable dye or finely divided pigment so as to provide a'marked contrast with the dust employed to develop the latent print, thereby increasing clarity and readability of the embedded print.
. The liquid coatingis preferably a fluid solution of a solid polymer dissolved in a volatile solvent, in which case setting of the applied coating can be rapidly achieved by evaporation of the solvent upon exposure of the large film surface to air. Such polymer solutions have the practical advantages of being preparable in the final form of use long in advance, of being packageable in a single container, and of requiring no further treatment to produce hardening. Films can be made from polymer solutions containing volatile solvents, which harden within a matter of minutes, in some cases as little as a minute or two. If desired, of course,-evaporation of the solvent and consequent hardening of the film can be speeded up by warming, but ordinarily this is not necessary.
Any natural or synthetic solid polymer can be employed forour purpose, which can be dissolved in a volatile solvent to form a fluid solution and which, after evaporation .of the solvent forms a strippable, flexible, preferably'non-tacky film, either iperse or by modification with conditioningv components, such. .as plasticizers dispersed tackiness inhibitors, and the like.
Illustrative examples of solid polymers, which can be employed in our process as solutions in:yolatile solvents,
includethe polyamideswhich are soluble in volatile solvents at ordinary temperatures, such as theN-alkoxyalkyl polyamide derivatives; acrylic and methacrylicresins and their, copolymers, such as polyacrylamide, polymerized unsaturated hydrocarbon and halogenated hydrocarbon;
propanol, isopropanol, acetone, methylene chloride, chloroform, trichloroethylene, carbon tetrachloride,- hexane, benzene, petroleum ether and other volatile petroleum solvents, methyl ethyl ketone, cyclohexane, tetrahydrofuran, etc. In some cases, cosolvent systems, such asv methylene chloride-methanol, chloroform methanol, ethanol-water, can be used for such reasons as improved solubility and reduced viscosity.-
The concentration of the dissolved polymer is not critical and is dictated only by such practical considerations asthe thickness of-film desired, the optium setting time for particular applications and the viscosity of the solution; About 5 to solutions areusually ade-:
quate. In general, it is not desirable to increasethe concentration of the polymer'to the point'where viscosityis so excessive as to make application ofa thin coating difficult. The concentration at which this occurs varies, of-eourse, with different polymers and different solvents.- Pl'as ticizers suitable for the particular polymer can be dissolved in the polymer-volatile solvent-solution. Some examples of a few of the plasticizers which "can be employed include dibutyl and dioctylphthalate,.dibutyl and diethyl sebacate, trioctyl, triphenyland tricresylphosphate, butyl stearate, diacetin, high molecular weight alcohols, such as octanol, decanol, and the like.-
Other conditioners, such as tackiness inhibitors, can also be dispersed in the polymer solution. In general, this will not be necessary,since-suitable polymers which form non-tacky films can readily be selected.-
Polymerizable liquids which can be. cured into a solid, strippable, flexible film after application to a surface can 4 a o a. p r ly redli uid n ym rts sh.ass ttaian ta. tially polymerized polyamidesya catalyst introduced into a liquid monomer, a mixture of copolymerizable monomers, or a partially cured liquid polymer such as a liquid siloxane, liquid polysulfide polymer, liquid polyester, liquid epoxy, and liquid polyamide; or a reactive atmospheric component such as oxygen or moisture, as in the case of partially cured polyurethanes which harden by reaction with moisture in the air, Such polymerizable liquids are entirely feasible for our purpose, although, in some instances they may require longer setting times than volatile solvent solutions of solid polymers or mixing with a copolymerizablecomponent or a catalyst shortly prior to use.
The liquid coatings can be applied to the surface bearing the dusted skin prints in any suitable and convenientmanner, although care should be taken not to apply it, in so forceful a manner as to disturb the dusted printas, V for example, by hard brushing. The liquid can be flowed. on as, for example, by dropping small amounts on the sur face and permitting it to flow into a film.
The most convenient mode of application is by spray-- ing, which can be accomplished in any desired manner. The solution can be sprayed from a manually operated container or from one pressurized by an inert gas such as nitrogen or carbon dioxide. It can also, in some cases, v be sprayed as an aerosol, Where the particular polymer solution is miscible with a propellant agent maintained in the liquid state at normal temperatures by the application of pressure. Such propellant agents include, for example, methyl'chloride and various chlorofluoro methanes and ethanes, such as dichlorodifiuoromethane (Freon-12), monochlorodifluoromethane (Freon-22), and dichlorotetrafiuoroethane (Freon-114) EXAMPLE I N-methoxymethyl polyarnide solutions were prepared bydissolving 10 grams. of the polyamide in 100 ml. of methylene chloride/methapolin ratios varying from 40:60- to 135, These formed clear, non-gelling solutions of low viscosity, which couldbe sprayed onto a surface to form thin, flexible, non-tacky, strippable solid films inabout 2 to 10 minutes. When the solutions were applied to a surface carrying fingerprints dusted with finely divided powders, such as carbon black or talc, the dust patterns embedded in the stripped film duplicated perfectly the pattern originally developed on the surface. The stripped films, when mounted on cards, formed permanent, fileable records of the lifted prints.
Table I summarizes other film-forming polymer solutions which we have prepared and found suitable for our also be'employed. The curing agent can be beat applied purpose. Table l Polymer Concen- Solvent Other additives tratlon a Polyisobutylene 2 Do 10 1% o Polyisobutylene 2 I Mlerocrystalllne wax 10 phr.
l l chloride 5 Eth i chi ide/ at he 1 e n ene or ac o O 5 'o Dlbutyl sebacate? l0 phr.
20 Methylenechloride 23 .do 20 I Di-2ethylhexylphthalate 5phr. 20 Di-2-ethylhexyl phthalate 10 phr. 20 Di-Z-ethylhexyl phthalate i 15 phr.. 20 20 Di-Q-ethylhcxyl phthalate 5 phr. 20 Di-2-ethylhexyl phthalate 10 phr. 20 Dl-Zethylhexyl phthalate 15 phr. 10 do 10 Cyggghexanone/methyl chloride 10 Tetrah ydrofuran .4. 10 Methylene chloride.
S'ee footnotes at end of table.
Table I-Continued Polymer Concen- Solvent Other additives tration Methylene chloride ..do 30 40 10 15 20 Do 30 Chlorosulfonated polyethylene (Hypalon). 10 2-chl0ro-l,3-butadiene polymer (neoprene) 10 do Balata 10 Carbon tetrachloride Grams per 100 ml. solvent.
1 Polymers having molecular weights of 100,000, 120,000, 150,000, 200,000, and 300,000 were all employed in preparing the filmiorming solutlo 2 Molecular weight 100,000. 3 Parts per 100 parts resin. Vinyl chloride/vinyl acetate 90/10 5 Fluorinated vinyl chloride-vinyl ester copolyrner.
Tacklness inhibitor. 1 Plastieizer to improve flexibility.
EXAMPLE II The following commercially obtainable polymer solutions can be sprayed to form non-tacky, strippable, flexible films, which are excellent for our purpose:
Cocoon 560 and Cocoon 501, solutions of vinyl chlo' ride-vinyl acetate copolymer in methyl ethyl ketone.
S-llS-E, a solution of a terpolymer of vinyl chloride, vinylidene chloride and methyl acrylate.
Hysol 6101-B, a solution of a partially cured epoxy resin which drys to form a non-tacky film.
EXAMPLE III A solution of N-methoxymethyl polyamide was prepared by dissolving 10 grams of the polymer in 100 ml. methanol/methylene chloride, 60/40. The solution was loaded into an aerosol container and pressurized with dichlorodifluoromethane (Freonl2) in a ratio of 50 parts polymer solution to 40 parts propellant liquid. The aerosol mixture was readily sprayed, forming films from 2 to 4 mls. in thickness with two passes of spray. The films were tack-free in less than 2 minutes and could be stripped in less than 10 minutes. The lifted imprints were clear and sharp.
EXAMPLE IV A commercially available aerosol solution of a polyacrylamide (Krylon #1301) produced satisfactory films when given a drying time of one-half hour after each pass.
EXAMPLE V Peroxide polymerization catalysts were added to the following liquid silicone polymers and the catalyzed liquid applied as a film and allowed to set.
(A) Silastic QS5330. Curing was complete in 5 minutes.
(B) Silicone 81712. Curing was complete in 1 hour.
The resulting films were flexible, non-tacky and strippable.
Although this invention has been described with reference to illustrative embodiments thereof, it will be apparent to those skilled in the art that the principles of this invention can be embodied in other inventions but within the scope of the claims.
We claim:
1. A process for lifting a latent skin imprint from a non-skin surface which comprises developing said imprint by dusting with a finely divided powder, coating the surface carrying the dusted imprint with a liquid composition consisting essentially of a polymer settable into a solid flexible, substantially non-tacky, strippable film, said dusting powder being insoluble in said liquid composition, setting the coating into a solid film, and separating the" film from said surface, said stripped film carrying embedded therein the finely divided powder in the pattern of said skin imprint.
2. A process for lifting a latent skin imprint from a non-skin surface which comprises developing said imprint by dusting with a finely divided powder, coating the surface carrying the dusted imprint with a liquid composition consisting essentially of a solution of a solid polymer dissolved in a volatile solvent, said liquid coating, upon evaporation of the volatile solvent, forming a solid, flexible, substantially non-tacky, strippable film, said dusting powder being insoluble in said liquid composition, permitting said coating to set into a solid film, and separating the film from said surface, said stripped film carrying embedded therein the finely divided powder in the pattern of said skin imprint.
3. The process of claim 2 in which the liquid coating composition is a solution of a polyamide which is soluble in a volatile solvent at ordinary temperatures.
4. The process of claim 3 in which the liquid coating composition is a solution of an N-alkoxyalkyl polyamide in a mixture of methylene chloride and methanol.
5. The process of claim 4 in which the N-alkoxyalkyl substituent is N-methoxymethyl and the ratio of methylene chloride to methanol is from about 40:60 to :35.
6. The process of claim 5 in which the polymer solution is admixed with a miscible propellant liquid which is maintained in the liquid state at normal temperatures by the application of pressure.
7. The process of claim 6 in which the propellant liquid is dichloro-difluoromethane.
8. The process of claim 2 in which the polymer is a. vinyl polymer.
9. The process of claim 8 in which the polymer is a vinyl chloride copolymerized with vinyl acetate.
10. The process of claim 2 in which the polymer is a vinyl polymer containing chlorine and fluorine substitucuts.
11. The process of claim 1 in which the polymer is a liquid silicone.
References Cited in the file of this patent UNITED STATES PATENTS 1,259,981 Hedrick Mar. 19, 1918 1,497,972 Bock June 17, 1924 1,833,287 Hadley Nov. 24, 1931 1,937,575 Joyce Dec. 5, 1933 1,951,203 Pitman Mar. 13, 1934 2,020,376 Rich Nov. 12, 1935 2,238,073 Patten Apr. 15, 1941 (Other references on following page) 7 3,. E UNITED STATES PATENTS FOREIGNPATENTS 2,312,913- Kirby -Mar. 2, 1943v 594,075 Grgaglirjtain Nov. 3, 1947 2,313,807: Gurry Mar. 16, 1943 r 2,615,820 Schwoegler Oct. 28, 1952 OTHER REFERENCES 2,634,216 Pineles er a1. Apr. 7, 1953 Surface Finish of Reduction Gear Teeth, by J. A. 2,639,216 Barth May 19, 1953 Davies, dated 1945. Class 18-'--Reshape Digest. 2,744,628 Engstrum Dec. 18, 1 956 2,819,196 Munro Jah. 7, 1958
Claims (1)
1. A PROCESS FOR LIFTING A LATENT SKIN IMPRINT FROM A NON-SKIN SURFACE WHICH COMPRISES DEVELOPING SAID IMPRINT BY DUSTING WITH A FINELY DIVIDED POWDER, COATING THE SURFACE CARRYING THE DUSTED IMPRINT WITH A LIQUID COMPOSITION CONSISTING ESSENTIALLY OF A POLYMER SETTABLE INTO A SOLID FLEXIBLE, SUBSTANTIALLY NON-TACKY, STRIPPABLE FILM, SAID DUSTING POWDER BEING INSOLUBLE IN SAID LIQUID COMPOSITION, SETTING THE COATING INTO A SOLID FILM, AND SEPARATING THE FILM FROM SAID SURFACE, SAID STRIPPED FILM CARRYING EMBEDDED THEREIN THE FINELY DIVIDED POWDER IN THE PATTERN OF SAID SKIN IMPRINT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US760071A US2986831A (en) | 1958-09-10 | 1958-09-10 | Process for lifting skin imprints |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US760071A US2986831A (en) | 1958-09-10 | 1958-09-10 | Process for lifting skin imprints |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2986831A true US2986831A (en) | 1961-06-06 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US760071A Expired - Lifetime US2986831A (en) | 1958-09-10 | 1958-09-10 | Process for lifting skin imprints |
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Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3029538A (en) * | 1961-06-15 | 1962-04-17 | Atlantic Res Corp | Process for taking skin prints |
| US3132036A (en) * | 1960-12-29 | 1964-05-05 | Herbert L Macdonell | Method of developing latent fingerprints |
| US3146144A (en) * | 1960-06-23 | 1964-08-25 | Jerome H Lemelson | Printing process |
| US3301046A (en) * | 1964-10-14 | 1967-01-31 | Kennedy F Rubert | Method of obtaining permanent record of surface flow phenomena |
| US3549397A (en) * | 1969-02-03 | 1970-12-22 | World Associates Inc | Method for developing finger prints |
| US4176205A (en) * | 1976-03-24 | 1979-11-27 | Rockwell International Corporation | Fingerprint powder and method of application |
| US4226740A (en) * | 1979-02-09 | 1980-10-07 | Criminalistics, Inc. | Infra-red responsive fingerprint composition and method of making |
| US4258073A (en) * | 1978-03-02 | 1981-03-24 | Payne John M | Taking of finger prints |
| US4426204A (en) | 1981-08-05 | 1984-01-17 | Carl Schleicher & Schull Gmbh & Co. Kg | Process for the marking of carrierless polymeric membranes and asymmetric carrierless polymeric membrane |
| WO1990015573A1 (en) * | 1989-06-16 | 1990-12-27 | The United States Department Of Energy | Fingerprint detection |
| US5281293A (en) * | 1992-06-08 | 1994-01-25 | Frame Curtis C | Device for lifting and processing latent fingerprints or other evidence |
| US20060165871A1 (en) * | 2005-01-27 | 2006-07-27 | Dierk Lubbers | Clear silicone material for the registration of fingerprints |
| US20080136159A1 (en) * | 2006-12-07 | 2008-06-12 | Jessica Lynn Zarate | Lifting and Preserving Bloody Impressions for Law Enforcement |
| US20100040765A1 (en) * | 2006-12-07 | 2010-02-18 | Jessica Lynn Zarate | Lifting and Preserving Bloody Impressions for Law Enforcement |
| US20100136208A1 (en) * | 2006-12-07 | 2010-06-03 | Jessica Lynn Zarate | Lifting and Preserving Bloody Impressions for Law Enforcement |
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| US1259981A (en) * | 1917-06-04 | 1918-03-19 | Edwin Hedrick | Method of fixing finger-prints. |
| US1497972A (en) * | 1921-06-01 | 1924-06-17 | Fingerprint Machine Corp | Composition for fingerprinting and method |
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| US1951203A (en) * | 1934-03-13 | Means fob transferring impressions | ||
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| US2238073A (en) * | 1938-11-18 | 1941-04-15 | Murray K Patten | Method of producing display sign material |
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| US2639216A (en) * | 1949-02-11 | 1953-05-19 | Diamond Alkali Co | Removal of halide ions from chromate liquors |
| US2744628A (en) * | 1952-10-18 | 1956-05-08 | Jeffrey Mfg Co | Jigging apparatus |
| US2819196A (en) * | 1954-06-09 | 1958-01-07 | Munro James Milton | Method of transferring a picture |
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| US1833287A (en) * | 1931-11-24 | louis | ||
| US1937575A (en) * | 1933-12-05 | Latent print lifting means | ||
| US1951203A (en) * | 1934-03-13 | Means fob transferring impressions | ||
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| US1259981A (en) * | 1917-06-04 | 1918-03-19 | Edwin Hedrick | Method of fixing finger-prints. |
| US1497972A (en) * | 1921-06-01 | 1924-06-17 | Fingerprint Machine Corp | Composition for fingerprinting and method |
| US2238073A (en) * | 1938-11-18 | 1941-04-15 | Murray K Patten | Method of producing display sign material |
| US2313807A (en) * | 1941-02-03 | 1943-03-16 | Gladys P Curry | Fingerprinting |
| US2312913A (en) * | 1941-08-18 | 1943-03-02 | Du Pont | Polyamide coated film element |
| GB594075A (en) * | 1943-07-01 | 1947-11-03 | Ici Ltd | Coated flexible sheet material |
| US2634216A (en) * | 1948-08-25 | 1953-04-07 | United Shoe Machinery Corp | Method for forming removable protective coverings |
| US2639216A (en) * | 1949-02-11 | 1953-05-19 | Diamond Alkali Co | Removal of halide ions from chromate liquors |
| US2615820A (en) * | 1949-03-01 | 1952-10-28 | Nox Rust Chemical Corp | Removable protective coating |
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Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3146144A (en) * | 1960-06-23 | 1964-08-25 | Jerome H Lemelson | Printing process |
| US3132036A (en) * | 1960-12-29 | 1964-05-05 | Herbert L Macdonell | Method of developing latent fingerprints |
| US3029538A (en) * | 1961-06-15 | 1962-04-17 | Atlantic Res Corp | Process for taking skin prints |
| US3301046A (en) * | 1964-10-14 | 1967-01-31 | Kennedy F Rubert | Method of obtaining permanent record of surface flow phenomena |
| US3549397A (en) * | 1969-02-03 | 1970-12-22 | World Associates Inc | Method for developing finger prints |
| US4176205A (en) * | 1976-03-24 | 1979-11-27 | Rockwell International Corporation | Fingerprint powder and method of application |
| US4258073A (en) * | 1978-03-02 | 1981-03-24 | Payne John M | Taking of finger prints |
| US4226740A (en) * | 1979-02-09 | 1980-10-07 | Criminalistics, Inc. | Infra-red responsive fingerprint composition and method of making |
| US4426204A (en) | 1981-08-05 | 1984-01-17 | Carl Schleicher & Schull Gmbh & Co. Kg | Process for the marking of carrierless polymeric membranes and asymmetric carrierless polymeric membrane |
| WO1990015573A1 (en) * | 1989-06-16 | 1990-12-27 | The United States Department Of Energy | Fingerprint detection |
| US5079029A (en) * | 1989-06-16 | 1992-01-07 | Saunders George C | Fingerprint detection |
| US5281293A (en) * | 1992-06-08 | 1994-01-25 | Frame Curtis C | Device for lifting and processing latent fingerprints or other evidence |
| US20060165871A1 (en) * | 2005-01-27 | 2006-07-27 | Dierk Lubbers | Clear silicone material for the registration of fingerprints |
| US8142833B2 (en) * | 2005-01-27 | 2012-03-27 | Coltene Ag | Clear silicone material for the registration of fingerprints |
| US20080136159A1 (en) * | 2006-12-07 | 2008-06-12 | Jessica Lynn Zarate | Lifting and Preserving Bloody Impressions for Law Enforcement |
| US20100040765A1 (en) * | 2006-12-07 | 2010-02-18 | Jessica Lynn Zarate | Lifting and Preserving Bloody Impressions for Law Enforcement |
| US20100136208A1 (en) * | 2006-12-07 | 2010-06-03 | Jessica Lynn Zarate | Lifting and Preserving Bloody Impressions for Law Enforcement |
| US8025852B2 (en) * | 2006-12-07 | 2011-09-27 | Jessica Lynn Zarate | Lifting and preserving bloody impressions for law enforcement |
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