US3218166A - Heat sensitive copy sheet - Google Patents
Heat sensitive copy sheet Download PDFInfo
- Publication number
- US3218166A US3218166A US239807A US23980762A US3218166A US 3218166 A US3218166 A US 3218166A US 239807 A US239807 A US 239807A US 23980762 A US23980762 A US 23980762A US 3218166 A US3218166 A US 3218166A
- Authority
- US
- United States
- Prior art keywords
- silver
- image
- reducing agent
- sheet
- soap
- 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
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- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 73
- 229910052709 silver Inorganic materials 0.000 claims description 73
- 239000004332 silver Substances 0.000 claims description 73
- 239000003638 chemical reducing agent Substances 0.000 claims description 63
- 239000000344 soap Substances 0.000 claims description 57
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 claims description 29
- 238000010438 heat treatment Methods 0.000 claims description 21
- IJAPPYDYQCXOEF-UHFFFAOYSA-N phthalazin-1(2H)-one Chemical compound C1=CC=C2C(=O)NN=CC2=C1 IJAPPYDYQCXOEF-UHFFFAOYSA-N 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 230000005855 radiation Effects 0.000 claims description 12
- AQRYNYUOKMNDDV-UHFFFAOYSA-M silver behenate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O AQRYNYUOKMNDDV-UHFFFAOYSA-M 0.000 claims description 12
- 150000007524 organic acids Chemical class 0.000 claims description 9
- 239000000376 reactant Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- 229940124024 weight reducing agent Drugs 0.000 description 58
- 239000011248 coating agent Substances 0.000 description 20
- 238000000576 coating method Methods 0.000 description 20
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 10
- 239000002131 composite material Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 6
- 150000002989 phenols Chemical class 0.000 description 6
- BOTGCZBEERTTDQ-UHFFFAOYSA-N 4-Methoxy-1-naphthol Chemical compound C1=CC=C2C(OC)=CC=C(O)C2=C1 BOTGCZBEERTTDQ-UHFFFAOYSA-N 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 4
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 4
- 150000004782 1-naphthols Chemical class 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
- 230000011514 reflex Effects 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 2
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 2
- YQUVCSBJEUQKSH-UHFFFAOYSA-N 3,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 235000021357 Behenic acid Nutrition 0.000 description 2
- 229920002799 BoPET Polymers 0.000 description 2
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
- 239000005041 Mylar™ Substances 0.000 description 2
- 229940116226 behenic acid Drugs 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000000586 desensitisation Methods 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- FBSFWRHWHYMIOG-UHFFFAOYSA-N methyl 3,4,5-trihydroxybenzoate Chemical compound COC(=O)C1=CC(O)=C(O)C(O)=C1 FBSFWRHWHYMIOG-UHFFFAOYSA-N 0.000 description 2
- -1 organic acid salts Chemical class 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229940079877 pyrogallol Drugs 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- YGOXSUSKUVELDI-UHFFFAOYSA-N 2,4,6-tris(2-methylbutan-2-yl)phenol Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=C(O)C(C(C)(C)CC)=C1 YGOXSUSKUVELDI-UHFFFAOYSA-N 0.000 description 1
- NICMVXRQHWVBAP-UHFFFAOYSA-N 2,6-ditert-butyl-4-octylphenol Chemical compound CCCCCCCCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NICMVXRQHWVBAP-UHFFFAOYSA-N 0.000 description 1
- MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 description 1
- ABJQKDJOYSQVFX-UHFFFAOYSA-N 4-aminonaphthalen-1-ol Chemical compound C1=CC=C2C(N)=CC=C(O)C2=C1 ABJQKDJOYSQVFX-UHFFFAOYSA-N 0.000 description 1
- DWRFAQWCIQVVFD-UHFFFAOYSA-N 4-methoxy-2-methylnaphthalen-1-ol Chemical compound C1=CC=C2C(OC)=CC(C)=C(O)C2=C1 DWRFAQWCIQVVFD-UHFFFAOYSA-N 0.000 description 1
- SXELZBOTXBNSQG-UHFFFAOYSA-N 4-methoxy-2-phenylnaphthalen-1-ol Chemical compound OC=1C2=CC=CC=C2C(OC)=CC=1C1=CC=CC=C1 SXELZBOTXBNSQG-UHFFFAOYSA-N 0.000 description 1
- FCPVSKGIQOYQRP-UHFFFAOYSA-N CCC.OC1=C(C2=CC=CC=C2C=C1)O.OC1=C(C2=CC=CC=C2C=C1)O Chemical compound CCC.OC1=C(C2=CC=CC=C2C=C1)O.OC1=C(C2=CC=CC=C2C=C1)O FCPVSKGIQOYQRP-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 206010044565 Tremor Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- PWAXUOGZOSVGBO-UHFFFAOYSA-N adipoyl chloride Chemical compound ClC(=O)CCCCC(Cl)=O PWAXUOGZOSVGBO-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 1
- 229940116224 behenate Drugs 0.000 description 1
- ZDZHCHYQNPQSGG-UHFFFAOYSA-N binaphthyl group Chemical group C1(=CC=CC2=CC=CC=C12)C1=CC=CC2=CC=CC=C12 ZDZHCHYQNPQSGG-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical group CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 239000006059 cover glass Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- IBKQQKPQRYUGBJ-UHFFFAOYSA-N methyl gallate Natural products CC(=O)C1=CC(O)=C(O)C(O)=C1 IBKQQKPQRYUGBJ-UHFFFAOYSA-N 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- XOOMNEFVDUTJPP-UHFFFAOYSA-N naphthalene-1,3-diol Chemical compound C1=CC=CC2=CC(O)=CC(O)=C21 XOOMNEFVDUTJPP-UHFFFAOYSA-N 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- ORYURPRSXLUCSS-UHFFFAOYSA-M silver;octadecanoate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCC([O-])=O ORYURPRSXLUCSS-UHFFFAOYSA-M 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- CVYDEWKUJFCYJO-UHFFFAOYSA-M sodium;docosanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O CVYDEWKUJFCYJO-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002344 surface layer Substances 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
- 239000002023 wood Substances 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
- G03C1/498—Photothermographic systems, e.g. dry silver
- G03C1/4989—Photothermographic systems, e.g. dry silver characterised by a thermal imaging step, with or without exposure to light, e.g. with a thermal head, using a laser
Definitions
- the film may contain a photosensitive aromatic hydroxy reducing agent, the image sheet then containing a water-insolublev silver 3,2'l8,166 Patented Nov. 16, 1965 ICC 2 z image sheet.
- the visible change occurring on uniformly heating the exposed intermediate film, with its remaining small amounts of photosensitive reducing agent at image areas, in contact with the image sheet containing the small amount of uniformly distributed non-photosensitive reducing agent, is of much greater intensity than could be ing comprising silver soap and a small amount of a light stable reducing agent.
- FIGURE 2 represents another embodiment in which both of -the reducing-agent cornponents are incorporated with the silver coating.
- the reducing agent is reactive with the silver soap at moderately elevated temperatures with liberation of free silver, accompanied by a visible change.
- Exposure to actinic radiation desensitizes the reducing agent, i.e. renders it nonreactive with the silver ion, and thus prevents occurrence of the image forming reaction at the I exposed areas when the two sheets are subsequentlyl heated in contacting face-to-face relationship.
- the reducing agents employed in the intermediate films are photosensitive, being rendered incapable of causing reduction of the silver ion when sut'- ciently 'exposed to actinic radiation.
- Other known reducing agents for silver ions-do not possess this property of photosen'sitivity, or are so slightly photosensitive as to be essentially, permanently stable under long continued exposure u'der ordi-nary storage and use conditions.v
- the incorporation of such materials into the silver soap coating of the image sheet causes pronounced darkening of the -sheet when heated.
- Excellent heat-sensitive copy sheets havey been made containing these light stable reducing agents inlintimate juxtaposition Withy the particles of v tion in the image or receptor sheet coating of certain essentially light-stable reducing agents for silver ion, and in significantly lesser amounts than normally required to produce desired image density on momentary heating-is effective-in providing fully defined, high density images while avoiding any darkening of background areas of the film, Mylar polyester film being thermographic copying procedure.
- y Paper is a preferrred substrate for the image sheet. Itmay be of any desired weight.
- the reactive coating may also be applied to other heat-resisting substrates, e.g. wood, glass, and fabric.
- the transparent carrier of the intermediate sheet will ordinarily be a thin plastic a preferred example. Thin unfilled paper is also useful.
- the reactive components will ordinarily be retained in place on the carrier or substrate by means of minimal amounts of film-forming binder materials. Suitable subcoats or prime coats may be used to insure proper bonding of the active coating, particularly on the transparent films.
- the reactants may alternatively be introduced into fibrous paper-like webs during the formation thereof -and in the substantial absence of any nlm-forming binder components.
- n Silver soaps of long-chain fatty acids e.g. silver behenate and silver stearate, are colorless, visibly stable ⁇ toward light, insoluble in many volatile liquid vehicles,
- Photosensitive reducing agents which have been found effective include l-hydroxy-rl-methoxy naphthalene, 1- hydroxy-2-methyl-4-methoxy naphthalene, l-hydroxy-4- ethoxy naphthalene, 4,4'dimethoxyl,1dihydroxy2,2' binaphthyl, l,l'-dihydroxy-LZ'-binaphthyl, 1,4-dihydroxy napthtalene, 1,3-dihydroxy naphthalene, 1-hydroxy-4- amino naphthalene, the bis-dihydroxynaphthalene-dimethylmethane condensation product of 1,5-dihydroxy naphthalene and acetone, 1-hydroxy-2-phenyl-4-methoxy naphthalene, the condensation product of two mols of 1,5-dihydroxynaphthalene and one mol of adipoyl chloride.
- the photosensitive reducing agent may be an alpha-naphthol having attached directly to the hydroxy. substituted aromatic ring a preponderance of electron donor groups which may be alkyl, aryl, alkoxy, aryloxy, hydroxy or amino.
- Readily volatile photosensitive reducing agents are employed in the intermediate sheet of the two-sheet composite; materials lof lesser volatility are Ti useful in unitary copy-sheets in which all of the reactants are contained in a single layer.
- a particularly effective light stable silver ion reducing agent which has given excellent results in the practice of the invention is 2,6-ditertiarybutyl-p-cresol, also known as Ionol or CAO-3.
- Ionol also known as Ionol or CAO-3.
- this material reduces the silver ionand produces a visible change when the sheet is heated for a somewhat longer time and at somewhat higher temperature than is normally the case in thermographic copying processes.
- the sheet fails to provide the required density of image when so heated, and remains virtually unchanged when heated for a time and at a temperature such as are ordinarily encountered in thermographic copying processes.
- the test is run as follows: a blend of 0.25 g. of silver behenate, 0.25 g. of the reducing agent, 0.05 g. of phthalazinone, and 3 ml. of methylethyl ketone is prepared by thorough mixing, yand a single drop of the mixture is placed on a small thin cover glass and allowed to dry. The glass is placed on the iiat surface of a metal plate heated to 100 C. and the time required to cause rapid darkening of the dry ilm is noted. It is assumed that the sample reaches the plate temperature within the first second, and accordingly no correction is applied for this period.
- a convenient means for obtaining the desired thorough mixing is an ordinary electrically driven high speed dental mixer. A few small glass beads may be added to assist in the mixing if desired. In any event the reactants must be thoroughly mixed so that the color change occurs uniformly throughout the entire ⁇ lm on the glass slide.
- test with p,pmethy1enebis(N,Ndimethyl aniline) requires some 70 seconds to develop full color change. With these materials the test mixture does not undergo the required rapid darkening, in which the full color change takes place within not more than one or two seconds, and usually even more rapidly.
- Ionol requiring six to eight seconds for the color change in the described test, provides intense blacliimage and clean white background areas when similarly employed.
- Other useful light stable reducing agents having analogous image amplifying properties, and the time required for them to produce rapid blackening in the test described, include: 2,6-ditertiarybutyl-li-methoxymethyl phenol, 8-9 seconds; 2,6-ditertiarybutyl-li-etbyl penol, 13-14 seconds; 2,6-ditertiarybutyl-4-octyl phenol, 17-20 seconds; p-cresol, 10 seconds; 2,4,6-tritertiaryamyl phenol, 25 seconds; and 4,4'methylenebis(2,6-ditertiarybutylphenol), l2 seconds.
- a photosensitive volatilizable reducing agent in the intermediate sheet permits the 'preparation of reproductions of graphie originals capable of providing differential light images and is ordinarily preferred.
- Other reducing agents may be substituted where heat images are to be employed, as in direct thermographic copying or in printing with heated metal typeor stylus.
- the coating on the intermediate film may contain pyrogallol or catechol in place of l-hydroxy-4-methoxy naphthalene, and images may be produced on animage sheet containing silver soap and small amounts of Ionol by locally heating the intermediate lm at image areas in contact with the image sheet.
- reducing agents with Ionol or i the like and withthe silver soap in a one-sheet heat-sensitive copy-paper which may at the same time be photosensitive if desired.
- a combination of silvery behenate, phthalazinone, Ionol and 1-hydroxy-4-methoxy naphthalene provides a coating which converts rapidly to an intense black on brief heating ybut which after exposure to actinic light does not darken beyond a Weak brownish black even on prolonged heating.
- Example 1 A mixture of equal mol percent of silver behenate and behenic acid is prepared by reacting together one m01V of silver nitrate and two mols of sodium behenate, made from commercial behenic acid, in acidic aqueous medium.
- the Washed and dried precipitate is in the form of a fine powder fusing at about C. and melting to a liquid at about 175 C.
- a coating mixture is prepared by mixi the coating assuming a dull brownish black appearance when the sheet is heated, for example for 2 minutes at C.
- a light-sensitive film product is prepared by applying to one mil (.001 inch) Mylar transparent polyester film a thin uniform coating of a blend of 50 parts by weight of ethyl cellulose, 1.4 parts of 1-hydroxy-4-methoxynaphthalene, and 0.3 part of erythrosin B. The mixture is applied from solution in acetone. The weight of the dried coating is 0.2 gram per square foot.
- the film is placed with its coated surface in contact with a printed original having light-absorptive inked image areas on a reliective white paper background and which is then uniformly exposed through the film, i.e. in the reflex position, to intense illumination from a bank of tungsten filament lamps for a time just suliicient to desensitize the coating completely at the background areas.
- a typical exposure time may be 12-15 seconds.
- the image areas are also affected but to a significantly lesser extent due to absorption in the image areas of the graphic original of that portion of the actinic radiation not previously absorbed in the sensitive coating.
- the exposed film is next placed with its coated surface against the coated sheet surface and the composite is heated, for example between rolls or platens, for 4-5 seconds at 12S-140 C.
- a copy of the graphic original is produced on the coated sheet.
- the image areas are a dense black; the background areas remain visibly unchanged.
- Heating a similary exposed film in contact with a coated sheet from which the 2,6-di-t-butyl-4-methy1- phenol has been omitted produces a faint and incomplete copy of the original, with brownish image areas ⁇
- Films coated with much larger amounts of the 1-hydroxy-4- methoxynaphthalene and exposed to complete desensitization at background areas produce darker but still incomplete image areas when heated in contact with such silvercoated sheets, and require excessive exposure for desensitization.
- Example 2 Essentially the same results are obtained when the phthalazinone of the foregoing example is replaced with phthalic anhydride as the toner for the silver image. More specifically, the silver soap mixture differs from that of Example 1 in substituting 2.6 parts of phthalic acid for the 5.2 parts of phthalazinone, and by increasing the amount of 2,6-di-tertiary-butyl-Lt-methylpheibl from 2.2 parts to 8 parts. On heating the reflex-exposed lightsensitive film in Contact with the coated image paper, there is developed on the latter a blue-brown image.
- Example 3 An image sheet prepared as in Examples 1 and 2 with a silver soap coating on a paper-like carrier may be converted into a unitary copy-sheet by the application of a further coating over the silver soap layer.
- a mixture of 0.1 part by weight of 4-methoxy-l-naphthol, 5 parts of ethyl cellulose, and 95 parts of methanol is coated at a 3-mil orifice over the silver soap coating of an image sheet prepared as described in Example 1, and the sheet is dried, forming a unitary heat-sensitive copy sheet with which copies of graphic originals may be prepared by thermographic back-print copying procedures.
- Such copies may be desensitized against further heat-induced visible change in the unprinted areas by exposure to ultraviolet radiation.
- the sheet may first be exposed to an ultraviolet radiation image. as by exposure through a negative transparency or a stencil, and the unexposed areas then developed by heating to produce a visible pattern.
- a heat-sensitive copy sheet product capable o'f providing high contrast dense black images on a white background when briefly heated at image areas to conversion temperature within the approximate range of 90-150" C., said product containing, uniformly applied over a paperlike carrier and in position for heat-induced inter-reaction, reactants comprising a silver soap of an organic acid, a toner for the silver image, a di-tertiaryalkyl substituted phenol first reducing agent for the silver ion in an amount of at least about 0.01 mol per mol of silver soap and in- (i vsufiicient to form with said silver soap a dense image when briefly heated therewith, and a photosensitve different active-hydrogen aromatic organic second reducing agent for said silver ion in an amount no greater than that of said first reducing agent, said first reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at
- a heat-sensitive copy sheet product capable of providing high contrast dense black images on a white background when briefly heated at image areas to conversion temperature Within the approximate range of -150 C., said product containing, uniformly applied over a paperlike carrier and in position for heat-induced inter-reaction, reactants comprising a silver soap of an Iorganic acid, phthalazinone toner for the silver image, a di-tertiaryalkyl substituted phenol first reducing agent for the silver ion in an amount within the range of approximately 0.01 to 0.4 mol per mol of silver soap and insufficient to form with said silver soap a dense image
- said first reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at C. before rapidly dark
- said image sheet including a layer consisting essentially of a silver soap of an organic acid, a toner for the silver image, and a di-tertiaryalkyl substituted first reducing agent in an amount of at least about 0.01 mol per mol of said silver soap and insufficient to form with said silver soap a dense image on briey heating said image sheet at 150 C. and characterized as forming with an equal weight of silver behenate and onefifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C. before rapidly darkening at that temperature; said intermediate sheet having image and background areas, said image areas including a volatilizable activehydrogen aromatic organic second reducing agent for the silver ion.
- a two-sheet heat-sensitive copy sheet composite capable of providing high contrast dense black images on a White background when briey heated in face-to-face contact at image areas to conversion temperature Within the approximate range of 90-150 C. and comprising: an image sheet including a layer comprising a silver soap of an organic acid, a toner for the silver image, and a ditertiaryalkyl substituted phenol first reducing agent for the silver ion in an amount of at least about 0.01 mol per mol of silver soap and insufiicient to form with said silver soap a dense image when said sheet is briefly heated, said first reducing agent being further characterized as forming with an equal weight of silver behenate and onefifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C.
- an intermediate sheet including a photosensitve volatilizable active-hydrogen aromatic organic second reducing agent for said silver ion in a concentration no greater than that of said first reducing agent and which on exposure to actinic radiation is rendered incapable of reducing silver ion on briey heating with silver soap at 150 C.
- a two-sheet heat-sensitive copy sheet composite capable of providing high contrast dense black images on a white background when briefly heated in face-tofacc contact at image areas to conversion temperature within the approximate .range of 90-150 C. and comprising; an image sheet including a layer comprising a silver soap of an organic acid, phthalazinone toner for the silver image, and a di-tertiaryalkyl substituted phenol tirst reducing agent for the silver ion in an amount within the approximate rangcof 0.01 to 0.4 mol per mol of silver soap and insuliicient to lor-m ywith said silver soap a dense image when said sheet is bricliy heated, said iirst reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said weight ot ⁇ phthalazinone a uniformly blended trace deposit requiring at least six seconds prehcat at 100 C.
- an intermediate sheet including a photosensitive volatilizable substituted alpha-naphthol second reducing agent for said silver ion in a concentration no greater than that of said rst reducing agent and which on exposure to actiaic radiation is rendered incapable of reducing silver ion on briefly heating with silver soap at 150 C.
- the transparent intermediate sheet includes a transparent carrier film having a coating comprising the photosensitive second reducing agent and a photoreducible dye.
- a visible change consistingessentially of a silver soap of an organic acid, a toner for the silver image, and a di-tertiaryalkyl substituted phenol iirst reducing agent in an amount of at least about 0.01 mol per mol of said silver soap and insulicient to form with said silver soap a dense image on briefly heating said image sheet at 150 C.
- said first reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said Weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C. before rapidly darkening at that temperature.
- a visible change consisting essentially of a silver soap of an organic acid, phthalazinone toner for the silver image, and a di-tertiarya liyl substituted phenol rst reducing agent in an amount within the approximate range of 0.01 to 0.4 mol per mol of said silver soap and insuicient to form with said silver soap a dense image on briefly heating said image sheet at 150 C., said lirst reducing agent being further characterized as forming with an equal weight of silver behcnate and one-fifth said? weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds prcheat at 100 C. bcl lore rapidly darkening at that temperature.
- An image sheet comprising a paper-like backing and a coating thereon comprising a silver soap, phthalazinonc. and 2,6-ditertiarybutyl-p-ciesol, the amount of 2,6- ditertiarybutyl-p-cresol being within the approxiate range of 0.0i to 0.4 -mol per mol of silver soap and insuiiicient to form with said soap a dense image on briefly heating said image sheet at 150 C.
- a heat-sensitive copy sheet product capable of providing high contrast dense black images on a white background when hrictly heated at image areas to conversion temperature within the approximate range of -150 C., said product containing, in position for image-forming heat-induced interreaction, reactants comprising a silver soap ot an organic acid, a toner for the silver image, a ditertiarybutyl alkyl phenol reducing agent for silver ion in an amount of at least about 0.01 mol per mol of silver soap and insufficient to form with said silver soap a dense image when briefly heated therewith and further characterized as forming with an equal Weight of silver behenate and onc-fth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at C.
- a photosensitive alpha-naphthol reducing agent for silver ion which reducing agent on exposure to actinic radiation is rendered incapable of reducing silver ion in a test procedure involving briefly heating with silver soap at C.
- a heat-sensitive copy sheet product including an image sheet and a transparent intermediate sheet in faceto-face contact; said image sheet including a surface ⁇ layer comprising a silver soap of an organic acid, a toner for the silver image, and a 2,-ditertiaryalkyl-4-alkyl phenol reducing agent for silver ion in an amount of at least about 0.01 mol per mol of silver soap and insulticient to form with said silver soap a dense image on brieliy heating an image area of said image sheet, said phenol being further characterized as forming with an equal Weight of silver behenate and one-litth said Weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C.
- said intermediate sheet including a surface layer comprising a photosensitive alpha-naphthol reducing agent for silverfion, said alpha-naphthol being further characterized as being rendered incapable oi' reducing silver ion, in a test procedure involving brieily heating with silver soap at 150 C., by exposure to actinic radiation.
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Description
Nov. 16, 1965 HEAT J. L. REITTER SENSITIVE COPY SHEET led NOV. 23, 1962 INVENTOR.
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United States Patent 3,213,166 l HEAT SENSl'I'lVE COPY SHEET John L. Reiner, St. Paul, Minn., assigner to Minnesota Mining & Manufacturing Company, St. Paul, Minima corporation of Delaware n Filed Nov. 23, 1962, Ser. No. 239,807 14 Claims. (Cl. 96-67) This invention relates to the copying of graphic originals, including those printed in various colors as well as black and white, by processes whereby the visible copy is produced through the application of heat. The invention has particular reference to improved copy-sheet materials with which copies of superior image density and contrast are made possible.
Methods have recently been devised for producing copies of printed or other graphic originalsby first preferentially desensitizing a sensitive intermediate film at reflective background areas of the original through reflex` light exposure, and'then` heating the film in contact with;
asuitable receptor or'image sheet which is thereby visibly changed at areas corresponding to the'still sensitive image areas of the intermediate film. Typically, the film may contain a photosensitive aromatic hydroxy reducing agent, the image sheet then containing a water-insolublev silver 3,2'l8,166 Patented Nov. 16, 1965 ICC 2 z image sheet. The visible change occurring on uniformly heating the exposed intermediate film, with its remaining small amounts of photosensitive reducing agent at image areas, in contact with the image sheet containing the small amount of uniformly distributed non-photosensitive reducing agent, is of much greater intensity than could be ing comprising silver soap and a small amount of a light stable reducing agent. FIGURE 2 represents another embodiment in which both of -the reducing-agent cornponents are incorporated with the silver coating.
In the'association indicated in FIGURE 1, the two soap in a single (sheets form/'a heat-sensitive copy sheet product, stable under room-.temperature storage `but reactive to provide dense black image areas on the silver-coated sheet when locally heated, for example by momentary contact with soap. The reducing agent is reactive with the silver soap at moderately elevated temperatures with liberation of free silver, accompanied by a visible change. Exposure to actinic radiation desensitizes the reducing agent, i.e. renders it nonreactive with the silver ion, and thus prevents occurrence of the image forming reaction at the I exposed areas when the two sheets are subsequentlyl heated in contacting face-to-face relationship.
The amount of reducing agent present in the interheated metal type or a heated metal test bar, or by transfer of a heat pattern from a differentially radiation-absorptive original in heat-conductive contact with the comn posite and subjected briefly to intense irradiation in the therefore limited. Accordingly it has beenv found dimcult to obtain image areas having 'sufciently high optical density to provide fully satisfactory `contrast in the final copy. Toners and other such adivants are useful in pro viding darker image areas, materials such as phthalazinone being particularly effective, but such materials havel not completely solved the problem of obtaining fully defined, dense, high contrast images in copies prepared by the methods hereinabove outlined.
As previously notcd,.the reducing agents employed in the intermediate films are photosensitive, being rendered incapable of causing reduction of the silver ion when sut'- ciently 'exposed to actinic radiation. Other known reducing agents for silver ions-do not possess this property of photosen'sitivity, or are so slightly photosensitive as to be essentially, permanently stable under long continued exposure u'der ordi-nary storage and use conditions.v The incorporation of such materials into the silver soap coating of the image sheet causes pronounced darkening of the -sheet when heated. Excellent heat-sensitive copy sheets havey been made containing these light stable reducing agents inlintimate juxtaposition Withy the particles of v tion in the image or receptor sheet coating of certain essentially light-stable reducing agents for silver ion, and in significantly lesser amounts than normally required to produce desired image density on momentary heating-is effective-in providing fully defined, high density images while avoiding any darkening of background areas of the film, Mylar polyester film being thermographic copying procedure. y Paper is a preferrred substrate for the image sheet. Itmay be of any desired weight. The reactive coating may also be applied to other heat-resisting substrates, e.g. wood, glass, and fabric. The transparent carrier of the intermediate sheet will ordinarily be a thin plastic a preferred example. Thin unfilled paper is also useful.
The reactive components will ordinarily be retained in place on the carrier or substrate by means of minimal amounts of film-forming binder materials. Suitable subcoats or prime coats may be used to insure proper bonding of the active coating, particularly on the transparent films. The reactants may alternatively be introduced into fibrous paper-like webs during the formation thereof -and in the substantial absence of any nlm-forming binder components. n Silver soaps of long-chain fatty acids, e.g. silver behenate and silver stearate, are colorless, visibly stable `toward light, insoluble in many volatile liquid vehicles,
and moisture-resistant; and these materials either alone or blended with additional fatty acid are preferred for use in the invention, although many other readily reducible normally solid organic acid salts of noble metals are also useful.
Photosensitive reducing agents which have been found effective include l-hydroxy-rl-methoxy naphthalene, 1- hydroxy-2-methyl-4-methoxy naphthalene, l-hydroxy-4- ethoxy naphthalene, 4,4'dimethoxyl,1dihydroxy2,2' binaphthyl, l,l'-dihydroxy-LZ'-binaphthyl, 1,4-dihydroxy napthtalene, 1,3-dihydroxy naphthalene, 1-hydroxy-4- amino naphthalene, the bis-dihydroxynaphthalene-dimethylmethane condensation product of 1,5-dihydroxy naphthalene and acetone, 1-hydroxy-2-phenyl-4-methoxy naphthalene, the condensation product of two mols of 1,5-dihydroxynaphthalene and one mol of adipoyl chloride.
. More generally, the photosensitive reducing agent may be an alpha-naphthol having attached directly to the hydroxy. substituted aromatic ring a preponderance of electron donor groups which may be alkyl, aryl, alkoxy, aryloxy, hydroxy or amino. Readily volatile photosensitive reducing agents are employed in the intermediate sheet of the two-sheet composite; materials lof lesser volatility are Ti useful in unitary copy-sheets in which all of the reactants are contained in a single layer.
A particularly effective light stable silver ion reducing agent which has given excellent results in the practice of the invention is 2,6-ditertiarybutyl-p-cresol, also known as Ionol or CAO-3. Combined in small proportions with the silver soap and phthalazinone toner in the image sheet coating, e.g. within the approximate limits of 0.01 to 0.4 mol per mol of silver soap, this material reduces the silver ionand produces a visible change when the sheet is heated for a somewhat longer time and at somewhat higher temperature than is normally the case in thermographic copying processes. However the sheet fails to provide the required density of image when so heated, and remains virtually unchanged when heated for a time and at a temperature such as are ordinarily encountered in thermographic copying processes. At considerably higher concentrations of the Ionol, for exam ple at equal molar concentrationswith the silver soap, an excellent light stable heat-sensitive copysheet is produced. The transfer of extremely small amounts of a photosensitive silver ion reducing agent such as 1hydroxy 4-rnethoxy naphthalene to the Ionol-deiicient coated sheet followed by brief heating at thermographic temperatures, i.e. within the approximate range of 90 to 150 C., results in the formation of visible images of high density. The amount of 1-hydroxy-4-methoxy naphthalene required is far less than the additional amount of Ionol which must be employed to provide comparable image density, and the time andternperature requirements are also reduced.
A number of other nonphotosensitive or light stable reducing agents for silver ion have also been found useful in the practice of the invention. It has been found impossible adequately to define these materials in terms of common structure or formula. However it has been found that those active-hydrogen aromatic organic reducing agents are useful which are characterized by requiring an induction period of at least about six seconds at 100 C. before reactingv rapidly with silver beben-ate and phthalazinone to a dense blackmass.
The test is run as follows: a blend of 0.25 g. of silver behenate, 0.25 g. of the reducing agent, 0.05 g. of phthalazinone, and 3 ml. of methylethyl ketone is prepared by thorough mixing, yand a single drop of the mixture is placed on a small thin cover glass and allowed to dry. The glass is placed on the iiat surface of a metal plate heated to 100 C. and the time required to cause rapid darkening of the dry ilm is noted. It is assumed that the sample reaches the plate temperature within the first second, and accordingly no correction is applied for this period.
A convenient means for obtaining the desired thorough mixing is an ordinary electrically driven high speed dental mixer. A few small glass beads may be added to assist in the mixing if desired. In any event the reactants must be thoroughly mixed so that the color change occurs uniformly throughout the entire `lm on the glass slide.
With some materials a gradual darkening is observed over an extended heating period. As an example, the test with p,pmethy1enebis(N,Ndimethyl aniline) requires some 70 seconds to develop full color change. With these materials the test mixture does not undergo the required rapid darkening, in which the full color change takes place within not more than one or two seconds, and usually even more rapidly.
When tested as just described, many of the reducing agents ordinarily suggested for use with silver soap in thermographic heat-sensitive copy sheet formulations cause complete blackening of the test sample within the rst second or at most within two to four seconds; and these materials have been found ineffective for the purposes of the invention. Thus, methyl gallate requires one to two seconds; catechol and pyrogallol require less than one second; protocatechuic acid and spiroindane require four seconds. image sheets coated with mixtures of these compounds and silver soap show pronounced darkening at background areas, or almost no improvement in image area density, when heated in contact with a reflex-exposed intermediate lilm as hereinbefore described.
On the contrary, Ionol, requiring six to eight seconds for the color change in the described test, provides intense blacliimage and clean white background areas when similarly employed. Other useful light stable reducing agents having analogous image amplifying properties, and the time required for them to produce rapid blackening in the test described, include: 2,6-ditertiarybutyl-li-methoxymethyl phenol, 8-9 seconds; 2,6-ditertiarybutyl-li-etbyl penol, 13-14 seconds; 2,6-ditertiarybutyl-4-octyl phenol, 17-20 seconds; p-cresol, 10 seconds; 2,4,6-tritertiaryamyl phenol, 25 seconds; and 4,4'methylenebis(2,6-ditertiarybutylphenol), l2 seconds.
The use of a photosensitive volatilizable reducing agent in the intermediate sheet permits the 'preparation of reproductions of graphie originals capable of providing differential light images and is ordinarily preferred. Other reducing agents may be substituted where heat images are to be employed, as in direct thermographic copying or in printing with heated metal typeor stylus. As an example, the coating on the intermediate film may contain pyrogallol or catechol in place of l-hydroxy-4-methoxy naphthalene, and images may be produced on animage sheet containing silver soap and small amounts of Ionol by locally heating the intermediate lm at image areas in contact with the image sheet. It is also possible to combine other classes of reducing agents with Ionol or i the like and withthe silver soap in a one-sheet heat-sensitive copy-paper which may at the same time be photosensitive if desired. For example, a combination of silvery behenate, phthalazinone, Ionol and 1-hydroxy-4-methoxy naphthalene provides a coating which converts rapidly to an intense black on brief heating ybut which after exposure to actinic light does not darken beyond a Weak brownish black even on prolonged heating.
The following examples will serve further to illustrate but not to limit the invention.
Example 1 A mixture of equal mol percent of silver behenate and behenic acid is prepared by reacting together one m01V of silver nitrate and two mols of sodium behenate, made from commercial behenic acid, in acidic aqueous medium.
The Washed and dried precipitate is in the form of a fine powder fusing at about C. and melting to a liquid at about 175 C. A coating mixture is prepared by mixi the coating assuming a dull brownish black appearance when the sheet is heated, for example for 2 minutes at C.
Increasing the amount of 2,6-di-t-buty1-4-methyl-phenol component to 12.6 parts in the above formula produces a sheet which permanently darkens to an intense black when` briey heated, for example for 6 seconds at 100 C. or on momentary contact with a metal test bar at 120 C., and which therefore is effective as a heat-sensitive copy sheet in the thermographic copying of differentially radiationabsorptive graphic originals.
A light-sensitive film product is prepared by applying to one mil (.001 inch) Mylar transparent polyester film a thin uniform coating of a blend of 50 parts by weight of ethyl cellulose, 1.4 parts of 1-hydroxy-4-methoxynaphthalene, and 0.3 part of erythrosin B. The mixture is applied from solution in acetone. The weight of the dried coating is 0.2 gram per square foot.
The film is placed with its coated surface in contact with a printed original having light-absorptive inked image areas on a reliective white paper background and which is then uniformly exposed through the film, i.e. in the reflex position, to intense illumination from a bank of tungsten filament lamps for a time just suliicient to desensitize the coating completely at the background areas. A typical exposure time may be 12-15 seconds. The image areas are also affected but to a significantly lesser extent due to absorption in the image areas of the graphic original of that portion of the actinic radiation not previously absorbed in the sensitive coating.
The exposed film is next placed with its coated surface against the coated sheet surface and the composite is heated, for example between rolls or platens, for 4-5 seconds at 12S-140 C. A copy of the graphic original is produced on the coated sheet. The image areas are a dense black; the background areas remain visibly unchanged.
Heating a similary exposed film in contact with a coated sheet from which the 2,6-di-t-butyl-4-methy1- phenol has been omitted produces a faint and incomplete copy of the original, with brownish image areas` Films coated with much larger amounts of the 1-hydroxy-4- methoxynaphthalene and exposed to complete desensitization at background areas produce darker but still incomplete image areas when heated in contact with such silvercoated sheets, and require excessive exposure for desensitization.
Example 2 Essentially the same results are obtained when the phthalazinone of the foregoing example is replaced with phthalic anhydride as the toner for the silver image. More specifically, the silver soap mixture differs from that of Example 1 in substituting 2.6 parts of phthalic acid for the 5.2 parts of phthalazinone, and by increasing the amount of 2,6-di-tertiary-butyl-Lt-methylpheibl from 2.2 parts to 8 parts. On heating the reflex-exposed lightsensitive film in Contact with the coated image paper, there is developed on the latter a blue-brown image.
Example 3 An image sheet prepared as in Examples 1 and 2 with a silver soap coating on a paper-like carrier may be converted into a unitary copy-sheet by the application of a further coating over the silver soap layer. A mixture of 0.1 part by weight of 4-methoxy-l-naphthol, 5 parts of ethyl cellulose, and 95 parts of methanol is coated at a 3-mil orifice over the silver soap coating of an image sheet prepared as described in Example 1, and the sheet is dried, forming a unitary heat-sensitive copy sheet with which copies of graphic originals may be prepared by thermographic back-print copying procedures. Such copies may be desensitized against further heat-induced visible change in the unprinted areas by exposure to ultraviolet radiation. Alternatively, the sheet may first be exposed to an ultraviolet radiation image. as by exposure through a negative transparency or a stencil, and the unexposed areas then developed by heating to produce a visible pattern.
1. A heat-sensitive copy sheet product capable o'f providing high contrast dense black images on a white background when briefly heated at image areas to conversion temperature within the approximate range of 90-150" C., said product containing, uniformly applied over a paperlike carrier and in position for heat-induced inter-reaction, reactants comprising a silver soap of an organic acid, a toner for the silver image, a di-tertiaryalkyl substituted phenol first reducing agent for the silver ion in an amount of at least about 0.01 mol per mol of silver soap and in- (i vsufiicient to form with said silver soap a dense image when briefly heated therewith, and a photosensitve different active-hydrogen aromatic organic second reducing agent for said silver ion in an amount no greater than that of said first reducing agent, said first reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C. before rapidly darkening at that temperature, and said second reducing agent on exposure to actinic radiation being rendered incapable of reducing silver ion on briefly heating with silver soap at 150 C.
2. A heat-sensitive copy sheet product capable of providing high contrast dense black images on a white background when briefly heated at image areas to conversion temperature Within the approximate range of -150 C., said product containing, uniformly applied over a paperlike carrier and in position for heat-induced inter-reaction, reactants comprising a silver soap of an Iorganic acid, phthalazinone toner for the silver image, a di-tertiaryalkyl substituted phenol first reducing agent for the silver ion in an amount within the range of approximately 0.01 to 0.4 mol per mol of silver soap and insufficient to form with said silver soap a dense image When briefiy heated therewith, and a photosensitive substituted alpha-napthol second reducing agent for said silver ion in an amount no greater than that of said first reducing agent, said first reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at C. before rapidly darkening at that temperature, and said second reducing agent on exposure to actinic radiation being rendered incapable of reducing silver ion on briey heating with silver soap at C.
3. In combination for preparing a visible image, a two-sheet composite of an image sheet and an intermediate sheet in face-to-face contact; said image sheet including a layer consisting essentially of a silver soap of an organic acid, a toner for the silver image, and a di-tertiaryalkyl substituted first reducing agent in an amount of at least about 0.01 mol per mol of said silver soap and insufficient to form with said silver soap a dense image on briey heating said image sheet at 150 C. and characterized as forming with an equal weight of silver behenate and onefifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C. before rapidly darkening at that temperature; said intermediate sheet having image and background areas, said image areas including a volatilizable activehydrogen aromatic organic second reducing agent for the silver ion.
4. A two-sheet heat-sensitive copy sheet composite capable of providing high contrast dense black images on a White background when briey heated in face-to-face contact at image areas to conversion temperature Within the approximate range of 90-150 C. and comprising: an image sheet including a layer comprising a silver soap of an organic acid, a toner for the silver image, and a ditertiaryalkyl substituted phenol first reducing agent for the silver ion in an amount of at least about 0.01 mol per mol of silver soap and insufiicient to form with said silver soap a dense image when said sheet is briefly heated, said first reducing agent being further characterized as forming with an equal weight of silver behenate and onefifth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C. before rapidly darkening at that temperature; and an intermediate sheet including a photosensitve volatilizable active-hydrogen aromatic organic second reducing agent for said silver ion in a concentration no greater than that of said first reducing agent and which on exposure to actinic radiation is rendered incapable of reducing silver ion on briey heating with silver soap at 150 C.
5. A two-sheet heat-sensitive copy sheet composite capable of providing high contrast dense black images on a white background when briefly heated in face-tofacc contact at image areas to conversion temperature within the approximate .range of 90-150 C. and comprising; an image sheet including a layer comprising a silver soap of an organic acid, phthalazinone toner for the silver image, and a di-tertiaryalkyl substituted phenol tirst reducing agent for the silver ion in an amount within the approximate rangcof 0.01 to 0.4 mol per mol of silver soap and insuliicient to lor-m ywith said silver soap a dense image when said sheet is bricliy heated, said iirst reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said weight ot` phthalazinone a uniformly blended trace deposit requiring at least six seconds prehcat at 100 C. before rapidly darkening at that temperature; and an intermediate sheet including a photosensitive volatilizable substituted alpha-naphthol second reducing agent for said silver ion in a concentration no greater than that of said rst reducing agent and which on exposure to actiaic radiation is rendered incapable of reducing silver ion on briefly heating with silver soap at 150 C.
6. A two-sheet composite as deiined in claim 4 in which the intermediate sheet is transparent.
7. A two-sheet composite as defined in claim 5 in which the intermediate sheet is transparent.
8. A two-sheet composite as defined in claim 6 in which the transparent intermediate sheet includes a transparent carrier film having a coating comprising the photosensitive second reducing agent and a photoreducible dye.
Si. A two-sheet composite as defined in claim 7 in which the transparent intermediate sheet includes a transparent carrier film having a coating comprising the photoscasitive second reducing agent and a photoreducible dye.
10. Animage sheet for forming dense black images on brief exposure, at a conversion temperature within the approximate range of 90 to 150 C., to trace amounts of a volatilizable substituted alpha-naphthol second silver ion reducing agent, said sheet including a layer requiring extended exposure to a temperature in excess of 150 C. to produce a visible change and consistingessentially of a silver soap of an organic acid, a toner for the silver image, and a di-tertiaryalkyl substituted phenol iirst reducing agent in an amount of at least about 0.01 mol per mol of said silver soap and insulicient to form with said silver soap a dense image on briefly heating said image sheet at 150 C., said first reducing agent being further characterized as forming with an equal weight of silver behenate and one-fifth said Weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C. before rapidly darkening at that temperature.
lll. An image sheet for tor-ming dense black images on brief exposure, at a conversion temperature within the approximate range of 90 to 150 C., to trace amounts ot a volatilizabie substituted alpha-naphthol second silver ion reducing agent, said sheet including a layer requiring extended exposure to a temperature in excess of 150 C. to produce a visible change and consisting essentially of a silver soap of an organic acid, phthalazinone toner for the silver image, and a di-tertiarya liyl substituted phenol rst reducing agent in an amount within the approximate range of 0.01 to 0.4 mol per mol of said silver soap and insuicient to form with said silver soap a dense image on briefly heating said image sheet at 150 C., said lirst reducing agent being further characterized as forming with an equal weight of silver behcnate and one-fifth said? weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds prcheat at 100 C. bcl lore rapidly darkening at that temperature.
l2. An image sheet comprising a paper-like backing and a coating thereon comprising a silver soap, phthalazinonc. and 2,6-ditertiarybutyl-p-ciesol, the amount of 2,6- ditertiarybutyl-p-cresol being within the approxiate range of 0.0i to 0.4 -mol per mol of silver soap and insuiiicient to form with said soap a dense image on briefly heating said image sheet at 150 C.
13. A heat-sensitive copy sheet product capable of providing high contrast dense black images on a white background when hrictly heated at image areas to conversion temperature within the approximate range of -150 C., said product containing, in position for image-forming heat-induced interreaction, reactants comprising a silver soap ot an organic acid, a toner for the silver image, a ditertiarybutyl alkyl phenol reducing agent for silver ion in an amount of at least about 0.01 mol per mol of silver soap and insufficient to form with said silver soap a dense image when briefly heated therewith and further characterized as forming with an equal Weight of silver behenate and onc-fth said weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at C. before rapidly darkening at that temperature, and, in an amount no greater than that of said phenol, a photosensitive alpha-naphthol reducing agent for silver ion, which reducing agent on exposure to actinic radiation is rendered incapable of reducing silver ion in a test procedure involving briefly heating with silver soap at C.
14. A heat-sensitive copy sheet product including an image sheet and a transparent intermediate sheet in faceto-face contact; said image sheet including a surface `layer comprising a silver soap of an organic acid, a toner for the silver image, and a 2,-ditertiaryalkyl-4-alkyl phenol reducing agent for silver ion in an amount of at least about 0.01 mol per mol of silver soap and insulticient to form with said silver soap a dense image on brieliy heating an image area of said image sheet, said phenol being further characterized as forming with an equal Weight of silver behenate and one-litth said Weight of phthalazinone a uniformly blended trace deposit requiring at least six seconds preheat at 100 C. before rapidly darkening at that temperature; and said intermediate sheet including a surface layer comprising a photosensitive alpha-naphthol reducing agent for silverfion, said alpha-naphthol being further characterized as being rendered incapable oi' reducing silver ion, in a test procedure involving brieily heating with silver soap at 150 C., by exposure to actinic radiation.
References Cited by the Esaminer UNITED STATES PATENTS 2,910,377 10/1959 Owen IVI-36.9 3,074,809 1/1963 Owen 117-368 3,094,417 6/1963 Workman 117-369 3,094,619 6/1963 Grant 117-36.8
E WlLLlAhl D. MARTlN, Primary Examiner.
MURRAY KATZ, Examiner.
Claims (1)
1. A HEAT-SENSITIVE COPY SHEET PRODUCT CAPABLE OF PROVIDING HIGH CONTRAST DENSE BLACK IMAGES ON A WHITE BACKGROUND WHEN BRIEFLY HEATED AT IMAGE AREAS TO CONVERSION TEMPERATURE WITHIN THE APPROXIMATE RANGE OF 90-150*C., SAID PRODUCT CONTAINING, UNIFORMLY APPLIED OVER A PAPERLIKE CARRIER AND IN POSITION FOR HEAT-INDUCED INTER-REACTION, REACTANTS COMPRISING A SILVER SOAP OF AN ORGANIC ACID, A TONER FOR THE SILVER IMAGE, A DI-TERTIARYALKYL SUBSTITUTED PHENOL FIRST REDUCING AGENT FOR THE SILVER ION IN AN AMOUNT OF AT LEAST ABOUT 0.1 MOL PER MOL OF SILVER SOAP AND INSUFFICIENT TO FORM WITH SAID SILVER SOAP A DENSE IMAGE WHEN BRIEFLY HEATED THEREWITH, AND A PHOTOSENSITIVE DIFFERENT ACTIVE-HYDROGEN AROMATIC ORGANIC SECOND REDUCING AGENT FOR SAID SILVER ION IN AN AMOUNT NO GREATER THAN THAT OF SAID FIRST REDUCING AGENT, SAID FIRST REDUCING AGENT BEING FURTHER CHARACTERIZED AS FORMING WITH AN EQUAL WEIGHT OF SILVER BEHENATE AND ONE-FIFTH SAID WEIGHT OF PHTHALAZINONE A UNIFORMLY BLENDED TRACE DEPOSIT REQUIRING AT LEAST SIX SECONDS PREHEAT AT 100*C. BEFORE RAPIDLY DARKENING AT THAT TEMPERATURE, AND SAID SECOND REDUCING AGENT ON EXPOSURE TO ACITINIC RADIATION BEING RENDERED INCAPABLE OF REDUCING SILVER ION ON BRIEFLY HEATING WITH SILVER SOAP AT 150*C.
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DENDAT1250842D DE1250842B (en) | 1962-11-23 | Heat sensitive copying material | |
NL300853D NL300853A (en) | 1962-11-23 | ||
US239807A US3218166A (en) | 1962-11-23 | 1962-11-23 | Heat sensitive copy sheet |
GB44452/63A GB1071021A (en) | 1962-11-23 | 1963-11-11 | Copy-sheet product |
ES0293547A ES293547A1 (en) | 1962-11-23 | 1963-11-15 | Heat sensitive copy sheet |
BE640183A BE640183A (en) | 1962-11-23 | 1963-11-20 | |
SE12849/63A SE328472B (en) | 1962-11-23 | 1963-11-21 | |
CH1433663A CH454188A (en) | 1962-11-23 | 1963-11-22 | Heat-sensitive sheet-like copying material |
DK549463AA DK121305B (en) | 1962-11-23 | 1963-11-22 | Heat-sensitive copying material. |
FR954747A FR1383197A (en) | 1962-11-23 | 1963-11-22 | Heat sensitive copy sheet |
NL63300853A NL139485B (en) | 1962-11-23 | 1963-11-22 | HEAT-SENSITIVE COPY MATERIAL. |
AT940263A AT268875B (en) | 1962-11-23 | 1963-11-22 | Heat sensitive copier material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US239807A US3218166A (en) | 1962-11-23 | 1962-11-23 | Heat sensitive copy sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
US3218166A true US3218166A (en) | 1965-11-16 |
Family
ID=22903826
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US239807A Expired - Lifetime US3218166A (en) | 1962-11-23 | 1962-11-23 | Heat sensitive copy sheet |
Country Status (10)
Country | Link |
---|---|
US (1) | US3218166A (en) |
AT (1) | AT268875B (en) |
BE (1) | BE640183A (en) |
CH (1) | CH454188A (en) |
DE (1) | DE1250842B (en) |
DK (1) | DK121305B (en) |
ES (1) | ES293547A1 (en) |
GB (1) | GB1071021A (en) |
NL (2) | NL139485B (en) |
SE (1) | SE328472B (en) |
Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3409438A (en) * | 1963-08-26 | 1968-11-05 | Minnesota Mining & Mfg | Photosensitive heat developable copysheet |
US3446648A (en) * | 1965-09-27 | 1969-05-27 | Minnesota Mining & Mfg | Reactive copying sheet and method of using |
US3455687A (en) * | 1964-11-28 | 1969-07-15 | Eastman Kodak Co | Photothermographic copying process |
US3460946A (en) * | 1966-02-03 | 1969-08-12 | Minnesota Mining & Mfg | Image receptor sheets containing organic silver salts and metal ion image |
US3529963A (en) * | 1966-08-23 | 1970-09-22 | Du Pont | Image-yielding elements and processes |
US3547648A (en) * | 1968-01-26 | 1970-12-15 | Minnesota Mining & Mfg | Copy-sheet |
US3847612A (en) * | 1973-02-02 | 1974-11-12 | Minnesota Mining & Mfg | Light-sensitive heat-developable sheet material |
DE2440678A1 (en) * | 1974-08-24 | 1976-03-04 | Agfa Gevaert Ag | IMPROVED PHOTOGRAPHICAL RECORDING MATERIAL FOR THE PRODUCTION OF COPIES IN THE DRY PROCESS |
US4001026A (en) * | 1972-06-13 | 1977-01-04 | Agfa-Gevaert N.V. | Method and materials for thermoplastic recording |
US4123282A (en) * | 1975-09-08 | 1978-10-31 | Minnesota Mining And Manufacturing Company | Photothermographic toners |
EP0683428A1 (en) * | 1994-05-17 | 1995-11-22 | Agfa-Gevaert N.V. | Thermal transfer imaging system based on the heat transfer of a reducing agent for reducing a silver source to metallic silver |
EP0730196A2 (en) * | 1995-03-02 | 1996-09-04 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
US5558972A (en) * | 1994-06-27 | 1996-09-24 | Agfa-Gevaert | Thermal transfer printing of a reducing agent to a silver source contained in an image receiving layer |
US5587269A (en) * | 1994-03-25 | 1996-12-24 | Afga-Gevaert N.V. | Thermal transfer imaging process and donor element for use therein |
US5587268A (en) * | 1994-03-25 | 1996-12-24 | Agfa-Gevaert N.V. | Thermal transfer imaging process |
US5587270A (en) * | 1994-03-10 | 1996-12-24 | Agfa-Gevaert N.V. | Thermal imaging process and an assemblage of a donor and receiving element for use therein |
US5589317A (en) * | 1994-03-10 | 1996-12-31 | Agfa-Gevaert N.V. | Thermal transfer imaging process |
US5595854A (en) * | 1994-03-25 | 1997-01-21 | Agfa-Gevaert N.V. | Method for the formation of heat mode image |
US5601962A (en) * | 1994-03-25 | 1997-02-11 | Agfa-Gevaert N.V. | Thermal transfer process wherein a reducing agent and toning agent are transferred to a receiving element containing a thermoreducible silver source |
US5627008A (en) * | 1994-03-25 | 1997-05-06 | Agfa-Gevaert N.V. | Thermal transfer printing process using a mixture of reducing agents for image-wise reducing a silver source |
US5637550A (en) * | 1995-03-02 | 1997-06-10 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
EP0795997A1 (en) * | 1996-03-14 | 1997-09-17 | Agfa-Gevaert N.V. | Producing a contone image by sequentially exposing a thermo-sensitive imaging material by means of a set of radiation beams |
US5719005A (en) * | 1994-12-27 | 1998-02-17 | Agfa-Gevaert, N.V. | Method for the formation of an improved photo mode image |
EP1211093A1 (en) * | 2000-11-30 | 2002-06-05 | Agfa-Gevaert | Thermographic recording material with improved image tone |
US6586363B2 (en) | 2000-11-30 | 2003-07-01 | Agfa-Gevaert | Thermographic recording material with improved image tone |
US6664211B2 (en) | 2000-11-30 | 2003-12-16 | Agfa-Gevaert | Thermographic recording material with improved image tone |
US9125829B2 (en) | 2012-08-17 | 2015-09-08 | Hallstar Innovations Corp. | Method of photostabilizing UV absorbers, particularly dibenzyolmethane derivatives, e.g., Avobenzone, with cyano-containing fused tricyclic compounds |
US9145383B2 (en) | 2012-08-10 | 2015-09-29 | Hallstar Innovations Corp. | Compositions, apparatus, systems, and methods for resolving electronic excited states |
US9867800B2 (en) | 2012-08-10 | 2018-01-16 | Hallstar Innovations Corp. | Method of quenching singlet and triplet excited states of pigments, such as porphyrin compounds, particularly protoporphyrin IX, with conjugated fused tricyclic compounds have electron withdrawing groups, to reduce generation of reactive oxygen species, particularly singlet oxygen |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2220618C2 (en) * | 1972-04-27 | 1985-01-10 | Agfa-Gevaert Ag, 5090 Leverkusen | Image receiving material |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2910377A (en) * | 1956-06-28 | 1959-10-27 | Minnesota Mining & Mfg | Heat-sensitive copying-paper |
US3074809A (en) * | 1959-10-26 | 1963-01-22 | Minnesota Mining & Mfg | Heat-sensitive copying-paper |
US3094619A (en) * | 1961-01-03 | 1963-06-18 | Minnesota Mining & Mfg | Ultra-violet radiation-desensitizable thermographic copy-sheet and method |
US3094417A (en) * | 1961-01-03 | 1963-06-18 | Minnesota Mining & Mfg | Heat sensitive copy sheet, process of making and using |
-
0
- NL NL300853D patent/NL300853A/xx unknown
- DE DENDAT1250842D patent/DE1250842B/en active Pending
-
1962
- 1962-11-23 US US239807A patent/US3218166A/en not_active Expired - Lifetime
-
1963
- 1963-11-11 GB GB44452/63A patent/GB1071021A/en not_active Expired
- 1963-11-15 ES ES0293547A patent/ES293547A1/en not_active Expired
- 1963-11-20 BE BE640183A patent/BE640183A/xx unknown
- 1963-11-21 SE SE12849/63A patent/SE328472B/xx unknown
- 1963-11-22 NL NL63300853A patent/NL139485B/en not_active IP Right Cessation
- 1963-11-22 AT AT940263A patent/AT268875B/en active
- 1963-11-22 DK DK549463AA patent/DK121305B/en unknown
- 1963-11-22 CH CH1433663A patent/CH454188A/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2910377A (en) * | 1956-06-28 | 1959-10-27 | Minnesota Mining & Mfg | Heat-sensitive copying-paper |
US3074809A (en) * | 1959-10-26 | 1963-01-22 | Minnesota Mining & Mfg | Heat-sensitive copying-paper |
US3094619A (en) * | 1961-01-03 | 1963-06-18 | Minnesota Mining & Mfg | Ultra-violet radiation-desensitizable thermographic copy-sheet and method |
US3094417A (en) * | 1961-01-03 | 1963-06-18 | Minnesota Mining & Mfg | Heat sensitive copy sheet, process of making and using |
Cited By (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3409438A (en) * | 1963-08-26 | 1968-11-05 | Minnesota Mining & Mfg | Photosensitive heat developable copysheet |
US3455687A (en) * | 1964-11-28 | 1969-07-15 | Eastman Kodak Co | Photothermographic copying process |
US3446648A (en) * | 1965-09-27 | 1969-05-27 | Minnesota Mining & Mfg | Reactive copying sheet and method of using |
US3460946A (en) * | 1966-02-03 | 1969-08-12 | Minnesota Mining & Mfg | Image receptor sheets containing organic silver salts and metal ion image |
US3529963A (en) * | 1966-08-23 | 1970-09-22 | Du Pont | Image-yielding elements and processes |
US3547648A (en) * | 1968-01-26 | 1970-12-15 | Minnesota Mining & Mfg | Copy-sheet |
US4001026A (en) * | 1972-06-13 | 1977-01-04 | Agfa-Gevaert N.V. | Method and materials for thermoplastic recording |
US3847612A (en) * | 1973-02-02 | 1974-11-12 | Minnesota Mining & Mfg | Light-sensitive heat-developable sheet material |
DE2440678A1 (en) * | 1974-08-24 | 1976-03-04 | Agfa Gevaert Ag | IMPROVED PHOTOGRAPHICAL RECORDING MATERIAL FOR THE PRODUCTION OF COPIES IN THE DRY PROCESS |
US4013473A (en) * | 1974-08-24 | 1977-03-22 | Agfa-Gevaert N.V. | Recording materials and image receiving materials for producing copies in a dry way |
US4123282A (en) * | 1975-09-08 | 1978-10-31 | Minnesota Mining And Manufacturing Company | Photothermographic toners |
US5589317A (en) * | 1994-03-10 | 1996-12-31 | Agfa-Gevaert N.V. | Thermal transfer imaging process |
US5587270A (en) * | 1994-03-10 | 1996-12-24 | Agfa-Gevaert N.V. | Thermal imaging process and an assemblage of a donor and receiving element for use therein |
US5587269A (en) * | 1994-03-25 | 1996-12-24 | Afga-Gevaert N.V. | Thermal transfer imaging process and donor element for use therein |
US5587268A (en) * | 1994-03-25 | 1996-12-24 | Agfa-Gevaert N.V. | Thermal transfer imaging process |
US5595854A (en) * | 1994-03-25 | 1997-01-21 | Agfa-Gevaert N.V. | Method for the formation of heat mode image |
US5601962A (en) * | 1994-03-25 | 1997-02-11 | Agfa-Gevaert N.V. | Thermal transfer process wherein a reducing agent and toning agent are transferred to a receiving element containing a thermoreducible silver source |
US5627008A (en) * | 1994-03-25 | 1997-05-06 | Agfa-Gevaert N.V. | Thermal transfer printing process using a mixture of reducing agents for image-wise reducing a silver source |
US5547809A (en) * | 1994-05-17 | 1996-08-20 | Agfa-Gevaert, N.V. | Thermal transfer imaging system based on the heat transfer of a reducing agent for reducing a silver source to metallic silver |
EP0683428A1 (en) * | 1994-05-17 | 1995-11-22 | Agfa-Gevaert N.V. | Thermal transfer imaging system based on the heat transfer of a reducing agent for reducing a silver source to metallic silver |
US5558972A (en) * | 1994-06-27 | 1996-09-24 | Agfa-Gevaert | Thermal transfer printing of a reducing agent to a silver source contained in an image receiving layer |
US5719005A (en) * | 1994-12-27 | 1998-02-17 | Agfa-Gevaert, N.V. | Method for the formation of an improved photo mode image |
EP0730196A3 (en) * | 1995-03-02 | 1998-01-21 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
US5637550A (en) * | 1995-03-02 | 1997-06-10 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
EP0730196A2 (en) * | 1995-03-02 | 1996-09-04 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
EP0795997A1 (en) * | 1996-03-14 | 1997-09-17 | Agfa-Gevaert N.V. | Producing a contone image by sequentially exposing a thermo-sensitive imaging material by means of a set of radiation beams |
EP1211093A1 (en) * | 2000-11-30 | 2002-06-05 | Agfa-Gevaert | Thermographic recording material with improved image tone |
US6586363B2 (en) | 2000-11-30 | 2003-07-01 | Agfa-Gevaert | Thermographic recording material with improved image tone |
US6664211B2 (en) | 2000-11-30 | 2003-12-16 | Agfa-Gevaert | Thermographic recording material with improved image tone |
US9765051B2 (en) | 2012-08-10 | 2017-09-19 | Hallstar Innovations Corp. | Compositions, apparatus, systems, and methods for resolving electronic excited states |
US9145383B2 (en) | 2012-08-10 | 2015-09-29 | Hallstar Innovations Corp. | Compositions, apparatus, systems, and methods for resolving electronic excited states |
US9611246B2 (en) | 2012-08-10 | 2017-04-04 | Hallstar Innovations Corp. | Compositions, apparatus, systems, and methods for resolving electronic excited states |
US9867800B2 (en) | 2012-08-10 | 2018-01-16 | Hallstar Innovations Corp. | Method of quenching singlet and triplet excited states of pigments, such as porphyrin compounds, particularly protoporphyrin IX, with conjugated fused tricyclic compounds have electron withdrawing groups, to reduce generation of reactive oxygen species, particularly singlet oxygen |
US9926289B2 (en) | 2012-08-10 | 2018-03-27 | Hallstar Innovations Corp. | Compositions, apparatus, systems, and methods for resolving electronic excited states |
US10632096B2 (en) | 2012-08-10 | 2020-04-28 | HallStar Beauty and Personal Care Innovations Company | Method of quenching singlet and triplet excited states of photodegradable pigments, such as porphyrin compounds, particularly protoporphyrin IX, with conjugated fused tricyclic compounds having electron withdrawing groups, to reduce generation of singlet oxygen |
US9125829B2 (en) | 2012-08-17 | 2015-09-08 | Hallstar Innovations Corp. | Method of photostabilizing UV absorbers, particularly dibenzyolmethane derivatives, e.g., Avobenzone, with cyano-containing fused tricyclic compounds |
Also Published As
Publication number | Publication date |
---|---|
NL139485B (en) | 1973-08-15 |
DE1250842B (en) | 1967-09-28 |
AT268875B (en) | 1969-02-25 |
NL300853A (en) | |
BE640183A (en) | 1964-03-16 |
SE328472B (en) | 1970-09-14 |
CH454188A (en) | 1968-04-15 |
DK121305B (en) | 1971-10-04 |
ES293547A1 (en) | 1964-01-01 |
GB1071021A (en) | 1967-06-07 |
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