US3080254A - Heat-sensitive copying-paper - Google Patents
Heat-sensitive copying-paper Download PDFInfo
- Publication number
- US3080254A US3080254A US84854959A US3080254A US 3080254 A US3080254 A US 3080254A US 84854959 A US84854959 A US 84854959A US 3080254 A US3080254 A US 3080254A
- Authority
- US
- United States
- Prior art keywords
- heat
- copy
- sheet
- sensitive
- atom
- 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
- IJAPPYDYQCXOEF-UHFFFAOYSA-N phthalazin-1(2H)-one Chemical compound C1=CC=C2C(=O)NN=CC2=C1 IJAPPYDYQCXOEF-UHFFFAOYSA-N 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- 239000003638 chemical reducing agent Substances 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 229910000510 noble metal Inorganic materials 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 150000002926 oxygen Chemical class 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 24
- 239000003795 chemical substances by application Substances 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 12
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- 239000010410 layer Substances 0.000 description 8
- 229910052709 silver Inorganic materials 0.000 description 8
- 239000004332 silver Substances 0.000 description 8
- AQRYNYUOKMNDDV-UHFFFAOYSA-M silver behenate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O AQRYNYUOKMNDDV-UHFFFAOYSA-M 0.000 description 7
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 235000021357 Behenic acid Nutrition 0.000 description 5
- 229940116226 behenic acid Drugs 0.000 description 5
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 5
- -1 cetyl protocatechuate Chemical compound 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000001556 precipitation Methods 0.000 description 5
- 230000033458 reproduction Effects 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000006479 redox reaction Methods 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 3
- 229940081974 saccharin Drugs 0.000 description 3
- 235000019204 saccharin Nutrition 0.000 description 3
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 3
- LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 description 2
- GLDQAMYCGOIJDV-UHFFFAOYSA-N 2,3-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC(O)=C1O GLDQAMYCGOIJDV-UHFFFAOYSA-N 0.000 description 2
- WXTMDXOMEHJXQO-UHFFFAOYSA-N 2,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC=C1O WXTMDXOMEHJXQO-UHFFFAOYSA-N 0.000 description 2
- CFFZDZCDUFSOFZ-UHFFFAOYSA-N 3,4-Dihydroxy-phenylacetic acid Chemical compound OC(=O)CC1=CC=C(O)C(O)=C1 CFFZDZCDUFSOFZ-UHFFFAOYSA-N 0.000 description 2
- IBGBGRVKPALMCQ-UHFFFAOYSA-N 3,4-dihydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1O IBGBGRVKPALMCQ-UHFFFAOYSA-N 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
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- KBPUBCVJHFXPOC-UHFFFAOYSA-N ethyl 3,4-dihydroxybenzoate Chemical compound CCOC(=O)C1=CC=C(O)C(O)=C1 KBPUBCVJHFXPOC-UHFFFAOYSA-N 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000463 material 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
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- DDWXNUFFAFBJDG-UHFFFAOYSA-N 1-acetyl-2-sulfanylideneimidazolidin-4-one Chemical compound CC(=O)N1CC(=O)NC1=S DDWXNUFFAFBJDG-UHFFFAOYSA-N 0.000 description 1
- 150000004782 1-naphthols Chemical class 0.000 description 1
- XIROXSOOOAZHLL-UHFFFAOYSA-N 2',3',4'-Trihydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C(O)=C1O XIROXSOOOAZHLL-UHFFFAOYSA-N 0.000 description 1
- 229940082044 2,3-dihydroxybenzoic acid Drugs 0.000 description 1
- FLFWJIBUZQARMD-UHFFFAOYSA-N 2-mercapto-1,3-benzoxazole Chemical compound C1=CC=C2OC(S)=NC2=C1 FLFWJIBUZQARMD-UHFFFAOYSA-N 0.000 description 1
- 150000004786 2-naphthols Chemical class 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- YRNWIFYIFSBPAU-UHFFFAOYSA-N 4-[4-(dimethylamino)phenyl]-n,n-dimethylaniline Chemical compound C1=CC(N(C)C)=CC=C1C1=CC=C(N(C)C)C=C1 YRNWIFYIFSBPAU-UHFFFAOYSA-N 0.000 description 1
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 1
- PZSCUHISJBQKSN-UHFFFAOYSA-N 4-methoxy-1,2-dihydronaphthalen-1-ol Chemical compound C1=CC=C2C(OC)=CCC(O)C2=C1 PZSCUHISJBQKSN-UHFFFAOYSA-N 0.000 description 1
- KABUZPWVPGUDIR-UHFFFAOYSA-N 5-nitro-1,1-dioxo-1,2-benzothiazol-3-one Chemical compound [O-][N+](=O)C1=CC=C2S(=O)(=O)NC(=O)C2=C1 KABUZPWVPGUDIR-UHFFFAOYSA-N 0.000 description 1
- KVOJTUXGYQVLAJ-UHFFFAOYSA-N 6,7-dihydroxy-4-methylcoumarin Chemical compound C1=C(O)C(O)=CC2=C1OC(=O)C=C2C KVOJTUXGYQVLAJ-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- RPWFJAMTCNSJKK-UHFFFAOYSA-N Dodecyl gallate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC(O)=C(O)C(O)=C1 RPWFJAMTCNSJKK-UHFFFAOYSA-N 0.000 description 1
- 229910003803 Gold(III) chloride Inorganic materials 0.000 description 1
- 241000147041 Guaiacum officinale Species 0.000 description 1
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- UQTCSFPVHNDUOG-UHFFFAOYSA-N azanium 4-carboxy-2,6-dihydroxyphenolate Chemical compound [NH4+].OC(=O)C1=CC(O)=C([O-])C(O)=C1 UQTCSFPVHNDUOG-UHFFFAOYSA-N 0.000 description 1
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 1
- 229940116224 behenate Drugs 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000000555 dodecyl gallate Substances 0.000 description 1
- 229940080643 dodecyl gallate Drugs 0.000 description 1
- 235000010386 dodecyl gallate Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- HLVGXGQCLASQJU-UHFFFAOYSA-N gallic acid anilide Natural products OC1=C(O)C(O)=CC(C(=O)NC=2C=CC=CC=2)=C1 HLVGXGQCLASQJU-UHFFFAOYSA-N 0.000 description 1
- RJHLTVSLYWWTEF-UHFFFAOYSA-K gold trichloride Chemical compound Cl[Au](Cl)Cl RJHLTVSLYWWTEF-UHFFFAOYSA-K 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229940091561 guaiac Drugs 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000002923 metal particle Substances 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
- JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- TXGSOSAONMOPDL-UHFFFAOYSA-N propan-2-yl 3,4,5-trihydroxybenzoate Chemical compound CC(C)OC(=O)C1=CC(O)=C(O)C(O)=C1 TXGSOSAONMOPDL-UHFFFAOYSA-N 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 229960003371 protocatechualdehyde Drugs 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- LVXAMCUUNGCSAK-UHFFFAOYSA-N silver benzene-1,4-diol nitrate Chemical compound C1(O)=CC=C(O)C=C1.[N+](=O)([O-])[O-].[Ag+] LVXAMCUUNGCSAK-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- FZHLWVUAICIIPW-UHFFFAOYSA-M sodium gallate Chemical compound [Na+].OC1=CC(C([O-])=O)=CC(O)=C1O FZHLWVUAICIIPW-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- CVYDEWKUJFCYJO-UHFFFAOYSA-M sodium;docosanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O CVYDEWKUJFCYJO-UHFFFAOYSA-M 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000011787 zinc oxide 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/913—Material designed to be responsive to temperature, light, moisture
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/165—Thermal imaging composition
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/166—Toner containing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31975—Of cellulosic next to another carbohydrate
- Y10T428/31978—Cellulosic next to another cellulosic
- Y10T428/31982—Wood or paper
Definitions
- This invention is concerned with improvements in heatsensitive copying-paper useful in preparing copies of differentially radiation-absorptive graphic originals, such as printed matter, by thermographic reproduction processes, for example as described in Miller Patent No. 2,740,896. More particularly, the invention concerns improved heatscnsitive copying-papers of the type described in Owen application Serial No. 594,540, tiled lune 28, 1956, now Patent No. 2,910,377, and in which the visible change obtained is a result of an oxidation-reduction reaction involving the liberation of a free metal.
- a typical heatdsensitive copy-paper of the type just identitied includes in the visibly heatesensitive layer a waterinsoluble silver salt, eg. silver stearato, and an appropriate organic reducing agent, of which 4-methoxy-l-hydroxydihydronaphthalene is representative.
- a waterinsoluble silver salt eg. silver stearato
- an appropriate organic reducing agent of which 4-methoxy-l-hydroxydihydronaphthalene is representative.
- the image areas t-hus formed are sharply outlined and distinctly visible, but normally differ considerably in color and general appearance from the corresponding areas of the printed or typewritten or other graphic original. In other instances the image areas may be yellowish, or greenish, or other less desirable color.
- Example l A mixture of equimolar proportions of auric behenate and behenic acid is first prepared by precipitation from a mixture of two mols of the water-soluble sodium salt of commercial behenic acid ⁇ and one mol of auric chloride. Five grams of the washed and dried product is intimately dispersed, by prolonged grinding in a ball mill, in a solution of 2 grams of polystyrene resin binder in 93 grams of a mixture of equal parts of acetone and commercial heptane. Separately there is prepared a solution of 3.75 grams of hydroquinone in a solution of 14.5 grams of the styrene resin in 8O grams of the solvent mixture.
- the dispersion of metal salt and solution of reducing agent are mixed in the ratio of 2 parts of the former to one part of the latter, and a rst portion of the mixture is applied in a thin uniform layer to map overlay tracing paper and dried at room temperature.
- the resulting sheet is a pale yellow in color. It changes to a reddish purple when placed in momentary contact with a suitably heated metal test bar or when employed in the thermographic reproduction process.
- Example 2 Silver behenate is prepared by precipitation from an equimolar mixture of silver nitrate and sodium behenate. The water-insoluble salt is washed, dried, and dispersed in a solution of polystyre-ne in methyl ethyl ketone. Hydroquinone is separately dissolved in a solution of polystyrene in a 1:1 mixture of acetone and heptane. Equal quantities of the two products are mixed together to form a mixture having the formula Parts ,by Weight Silver behenate l0 Hydroquinone 4 Binder 12 Volatile liquid vehicle 174 Toning Agent Gm./20 g Sheet Image Color Mixture Color (none) White. Yellow-brown.
- Example A rnixture of silver behenate and 10% behenic acid is iirst prepared, and 10 parts of the mixture then ball milled with a solution of 4 parts of ethyl cellulose in 86 parts of acetone. Three grams of spiroindane and 4 grams of ethyl cellulose are separately dissolved in 93 grams of acetone. Equal weights of dispersion and solution are mixed together, coated on a thin transparent carrier web at a thickness of two mils, and dried at room temperature.
- a further coating of a dispersion of 30 parts of zinc oxide and one part of silica gel in a solution of 3 parts of styreneisobutylene copolymer in 66 parts of commercial heptane is applied at 1.5 mils thickness and dried to form a contrasting white opaque protective layer.
- the sheet yields yellow-brown image areas visible through the transparent carrier when heated in the thermographic process or on the test bar. Copy produced on such sheets is distinct and vlegible ybut lacks esthetic appeal when contrasted lwith the black-on-white typed or printed original.
- Another copy-sheet is prepared in the same manner except that to the mixture of silver salt dispersion and reducing agent solution there is ii-rst added 2% of phthalazinone. Heat-image areas produced on this sheet are black, and the copy has substantially lthe appearance of the original.
- Example 4 A copy-sheet prepared as in Example 3 except that gum guaiac is substituted in equal amount for the Spiroindane produces heat-image areas which are yellowish green in color.
- the incorporation of two percent of phthalazinone (two parts in 16) parts or the coatable liquid mixture) results in the formation or" deep blueblack heat-image m'eas and in much more attractive copies.
- Example 5 A mix-ture of equal molar amounts of silver behenate and behenic acid is dispersed in a solution of polystyrene resin in a 1:1 mixture of acetone and heptane. Tertiarybutyl catechol is separately dissolved in another portion of the same binder solution. The two compositions are mixed together, a small amount of phthalazirionc is mixed in, and the mixture is coated on paper and dried. rl'he proportions of silver half soap, t-butyl -catechol, and phthalazinone are approximately 50:50zl. The resulting copy-sheet provides black images. In the absence of the phthalazinone the image areas obtained are yellowish brown.
- Phthalazinone is effective in small amounts, provides a particularly pleasing appearance to the heat-developed image areas without imparting any observable co-lor to the unheated portions, and is a preferred toning agent in my heat-sensitive copy-sheets.
- Barbituric acid, 2- benzoxazolethiol, and 1-ace-tyl-2-thiohydantoin are fully as effective as phthalazinone.
- Saccharin is somewhat less effective, and much larger amounts of this material are ⁇ ordinarily required, e.g. as indicated in connection with Example 2.
- Other examples of toning agents of about the same effectiveness as saccharin include: 5- nitrosaccharin; Z-hydroxybenzthiazole; imidazole; 2-
- the metal salt is suspended in a volatile vehicle such as methylethyl ketone, Ithe reducing agent is dissolved in the slurry, the mixture is spread over a test sheet, a few small particles or crystals of the compound bein-g tested are sprinkled over a portion of the coating and worked into the slurry with a stirring rod, the coating is permitted to dry, and the sheet is then placed into brief ⁇ contact with a metal test bar at conversion temperature.
- a volatile vehicle such as methylethyl ketone
- a solution of about one-half gram of hydroquinone in a slurry of one gram of silver behenate in l0 grams of methylethyl ketone is spread on a strip of white filter paper and powdered phthalazinone is dusted onto half of the coated area and mixed in.
- the coating dries rapidly.
- the dusted portion becomes black, whereas the remaining portions turn yellowish brown.
- the image-forming reaction involves the reduction of a noble metal salt to free metal in an oxidation-reduction reaction.
- Silver behenate is a preferred salt, being colorless, visibly stable toward light, insoluble in the volatile liquid vehicle, and moisture-resistant.
- the presence of free behenic acid increases the moisture-resistant properties of the sheet.
- the salt, with or without the free acid is produced in the desired physical form aad chemical purity without dicul-ty and at reasonable cost.
- Silver stearato has been successfully substituted for silver behenate, and silver salts of 'many other organic 'acids have also been found useful in these heat-sensitive compositions and copying-papers.
- a partial list of such organic acids includes oleic, lauric, hydroxystearic, acetic, phthalic, terephthalic, butyric, rn-nit-robenzoic, salicylic, phcnylacetic, pyromellitic, p-phenylbenzoic, undecylenic, camphoric, furoic, acetamidobenzoic and o-aminobenzoic.
- Reducing agents which have been found useful with such compounds in the formulation of heat-sensitive copy.
- - sheets include: pyrogallol; 4-azeloyl-'bis-pyrogallol; 4- istearoyl pyrogallol; galloacetophenone; di-tertiary-butyl pyrogallol; gallic acid anilide; methyl gallate, ethyl galllate; normaland iso-propyl gallate; lbutyl gallate; dodecyl gallate; gallic acid; ammonium gallate; ethyl protocatechuate; cetyl protocatechuate; 2,5-dihydroxy benzoic acid, l-hydroxy-Z-naphthoic acid; Z-hydroxy, S-naphthoic acid; phloroglucinol; catechol; 2,3-naphthalene diol; 4- lauroyl catechol; sodium gallate; protocatechualdehyde; 4-methyl esculet
- These compounds are cyclic or aromatic ⁇ compounds having an active hydrogen atom attached to an atom of carbon, oxygen or nitrogen which in turn is attached to an atom of the cyclic ring. They are capable of causing the reduction of silver ion and precipitation of metallic silver on being dissolved at moderate temperature in la solution of ⁇ aqueous silver nitrate in an organic solvent.
- the reactant materials are preferably applied to a ⁇ thin exible carrier or backing, such as paper or transparent film, in conjunction with a film-forming polymeric or resinous binder.
- the binder may itself serve the function of a carrier film; or the reactants may be supported in a fibrous web in the substantial absence of binder. Waxes, fibrous materials, pigments, fillers, dyes, fusible or infusible particulate materials, and various other additives may ⁇ be included for special purposes.
- the metal salt and organic reducing agent are preferably intermixcd prior to coating, but may be applied in separate but contiguous layers if desired, in which case the toning ,agent is present ⁇ at least in the metal salt layer.
- the size of the metal particles vaygipearing in the heated image areas of copy-sheets las hereinbefore described is significantly increased by the incorporation of the toning agent in the heat-sensitive layer.
- the silver particles precipitated from silver nitrate solution by addition of an acetone solution of hydroquinone or the like are found to have a dilferent shape and an increased apparent volume when precipitation occurs in the presence of a toning agent. increase in apparent volume of precipitate may also be observed on addition of small amounts of a toning agent to the silver nitrate-hydroquinone mixture after initial precipitation.
- silver metal as normally precipitated carries with it adsorbed silver ions; that the toning agents are acidic, or contain labile hydrogen atoms, and permit anion formation; that fusion of one or more of the components of the heat-sensitive coupling permits in effect van ionization of the acidic toning agent along with oxidation-reduction reaction of the maior reactants; that the resulting E anions then neutralize the adsorbed silver ions to permit the growth of particle size', and that the increased size of particles provides for increased internal reliection within the particles, resulting in a darker-appearing image.
- a heat-sensitive chemically reactive copy-sheet suitable for the preparation from diierentially radiationabsorptive graphic originals of thermographic reproductions having dark-colored image areas of pleasing appearance comprising a thin iiexible carrier web coated with a visibly heat-sensitive coating comprising (l) a lmJforrning binder, (2) a noble metal salt of -an organic acid, an-d (3) a cyclic organic reducing agent for the noble metal ions, having an active hydrogen atom attached to an atom which is selected from the class of oxygen, nitrogen and carbon atoms and is directly attached to an atom of the cyclic ring, and additionally including (4) va significant small proportion, suicient to cause observable darkening of the therrnographic image, of phthalazinone.
- a heat-sensitive chemically reactive copy-sheet suitable for the preparati-on, from differenti-ally radiationabsorptive graphic originals, of thermographic reproductions having dense black to blue-black image areas said copy-sheet including a visibly heat-sensitive layer comprising a chemically reactive heat-sensitive mixture of a silver salt of an organic acid and an organic reducing agent for the silver ions, and phthalazinone in a small amount suicient to cause observable darkening of the thermographic image.
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- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
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Description
March 5, 1963 E. A. GRANT, JR 3,080,254
HEAT-SENSITIVE COPYING-PAPER Filed Oct. 26, 1959 70/7//79 age/77'.' 50c/Qing.
Unite Stats 3,080,254 Patented Mar. 5, 1953 This invention is concerned with improvements in heatsensitive copying-paper useful in preparing copies of differentially radiation-absorptive graphic originals, such as printed matter, by thermographic reproduction processes, for example as described in Miller Patent No. 2,740,896. More particularly, the invention concerns improved heatscnsitive copying-papers of the type described in Owen application Serial No. 594,540, tiled lune 28, 1956, now Patent No. 2,910,377, and in which the visible change obtained is a result of an oxidation-reduction reaction involving the liberation of a free metal.
A typical heatdsensitive copy-paper of the type just identitied includes in the visibly heatesensitive layer a waterinsoluble silver salt, eg. silver stearato, and an appropriate organic reducing agent, of which 4-methoxy-l-hydroxydihydronaphthalene is representative. Localized heating of the sheet in the thermographic reproduction pnocess, or, for test purposes, by momentary contact with a metal test bar heated to .a suitable conversion temperaure in the range of about 90-l50 C., causes a visible change to occur in the heat-sensitive layer. The initially white or lightly colored layer is darkened to a brownish appearance at the heated area. The image areas t-hus formed are sharply outlined and distinctly visible, but normally differ considerably in color and general appearance from the corresponding areas of the printed or typewritten or other graphic original. In other instances the image areas may be yellowish, or greenish, or other less desirable color.
It has now been found that the color of the image areas obtained on heating these metal-liberating copy-sheets to conversion temperature may be desirably and leffectively darkened, so that the resulting copy appears in the form of dense black or 'blue-black images on an essentially white background. Copies of typewritten correspondence, printed pages and the like having essentially the appearance of the original are thereby made possible.
The just-described improvement in image appearance is achieved, in accordance with t-he principles of my invention, by including with the metal-liberating heat-sensitive composition a signiiicant small proportion of a heterocyclic organic toning agent containing at least two hetero atoms in the heterocyclic ring, of which at least one is Ia. nitrogen atom.
The following examples and the appended drawing describe specic heatesensitive copy-sheets illustrating the principles of the invention, which however is not to be construed as limited thereto.
Example l A mixture of equimolar proportions of auric behenate and behenic acid is first prepared by precipitation from a mixture of two mols of the water-soluble sodium salt of commercial behenic acid `and one mol of auric chloride. Five grams of the washed and dried product is intimately dispersed, by prolonged grinding in a ball mill, in a solution of 2 grams of polystyrene resin binder in 93 grams of a mixture of equal parts of acetone and commercial heptane. Separately there is prepared a solution of 3.75 grams of hydroquinone in a solution of 14.5 grams of the styrene resin in 8O grams of the solvent mixture. The dispersion of metal salt and solution of reducing agent are mixed in the ratio of 2 parts of the former to one part of the latter, and a rst portion of the mixture is applied in a thin uniform layer to map overlay tracing paper and dried at room temperature. The resulting sheet is a pale yellow in color. It changes to a reddish purple when placed in momentary contact with a suitably heated metal test bar or when employed in the thermographic reproduction process.
To a second portion of the liquid mixture is added 0.1% of phthalazinone. This portion likewise is applied to paper and dried, providing a heat-sensitive copy-paper which converts from pale yellow to deep blue-black when heated as just described.
Example 2 Silver behenate is prepared by precipitation from an equimolar mixture of silver nitrate and sodium behenate. The water-insoluble salt is washed, dried, and dispersed in a solution of polystyre-ne in methyl ethyl ketone. Hydroquinone is separately dissolved in a solution of polystyrene in a 1:1 mixture of acetone and heptane. Equal quantities of the two products are mixed together to form a mixture having the formula Parts ,by Weight Silver behenate l0 Hydroquinone 4 Binder 12 Volatile liquid vehicle 174 Toning Agent Gm./20 g Sheet Image Color Mixture Color (none) White. Yellow-brown.
0.05 ..-do Black. 0.08 ---do Do. Saccharin 0.3 -do Darkbrown-black.
Example A rnixture of silver behenate and 10% behenic acid is iirst prepared, and 10 parts of the mixture then ball milled with a solution of 4 parts of ethyl cellulose in 86 parts of acetone. Three grams of spiroindane and 4 grams of ethyl cellulose are separately dissolved in 93 grams of acetone. Equal weights of dispersion and solution are mixed together, coated on a thin transparent carrier web at a thickness of two mils, and dried at room temperature. A further coating of a dispersion of 30 parts of zinc oxide and one part of silica gel in a solution of 3 parts of styreneisobutylene copolymer in 66 parts of commercial heptane is applied at 1.5 mils thickness and dried to form a contrasting white opaque protective layer. The sheet yields yellow-brown image areas visible through the transparent carrier when heated in the thermographic process or on the test bar. Copy produced on such sheets is distinct and vlegible ybut lacks esthetic appeal when contrasted lwith the black-on-white typed or printed original.
Another copy-sheet is prepared in the same manner except that to the mixture of silver salt dispersion and reducing agent solution there is ii-rst added 2% of phthalazinone. Heat-image areas produced on this sheet are black, and the copy has substantially lthe appearance of the original.
Example 4 A copy-sheet prepared as in Example 3 except that gum guaiac is substituted in equal amount for the Spiroindane produces heat-image areas which are yellowish green in color. The incorporation of two percent of phthalazinone (two parts in 16) parts or the coatable liquid mixture) results in the formation or" deep blueblack heat-image m'eas and in much more attractive copies.
Similarly, the substitution of l,5dihydroxynaphthalene for the spiroindane of Example 3 results in a heat-sensitive copy-sheet which normally provides yellowish brown image areas, but with small amounts of phthaliazinone provides black images.
Example 5 A mix-ture of equal molar amounts of silver behenate and behenic acid is dispersed in a solution of polystyrene resin in a 1:1 mixture of acetone and heptane. Tertiarybutyl catechol is separately dissolved in another portion of the same binder solution. The two compositions are mixed together, a small amount of phthalazirionc is mixed in, and the mixture is coated on paper and dried. rl'he proportions of silver half soap, t-butyl -catechol, and phthalazinone are approximately 50:50zl. The resulting copy-sheet provides black images. In the absence of the phthalazinone the image areas obtained are yellowish brown.
Phthalazinone is effective in small amounts, provides a particularly pleasing appearance to the heat-developed image areas without imparting any observable co-lor to the unheated portions, and is a preferred toning agent in my heat-sensitive copy-sheets. Barbituric acid, 2- benzoxazolethiol, and 1-ace-tyl-2-thiohydantoin are fully as effective as phthalazinone. Saccharin is somewhat less effective, and much larger amounts of this material are `ordinarily required, e.g. as indicated in connection with Example 2. Other examples of toning agents of about the same effectiveness as saccharin include: 5- nitrosaccharin; Z-hydroxybenzthiazole; imidazole; 2-
thiazole; and l\T,N-ethylenethiourea.
The effectiveness of the toning action obtained with these and other equivalent nitrogen-containing heterocyclic toning agents will vary with the particular toning agent and the amount thereof, and with the specific natu-re of the noble metal salt and the organic reducing agent, and with other factors. A test procedure is available, however, by means of which effective toning agents may be selected for any speelt-led composition. in this test, the metal salt is suspended in a volatile vehicle such as methylethyl ketone, Ithe reducing agent is dissolved in the slurry, the mixture is spread over a test sheet, a few small particles or crystals of the compound bein-g tested are sprinkled over a portion of the coating and worked into the slurry with a stirring rod, the coating is permitted to dry, and the sheet is then placed into brief` contact with a metal test bar at conversion temperature. For example, a solution of about one-half gram of hydroquinone in a slurry of one gram of silver behenate in l0 grams of methylethyl ketone is spread on a strip of white filter paper and powdered phthalazinone is dusted onto half of the coated area and mixed in. The coating dries rapidly. When placed on a metal rod heated to 120 C., the dusted portion becomes black, whereas the remaining portions turn yellowish brown. With compounds which have no toning action, no observable difference in color is obtained between the two areas of the test strip.
The image-forming reaction involves the reduction of a noble metal salt to free metal in an oxidation-reduction reaction. Silver behenate is a preferred salt, being colorless, visibly stable toward light, insoluble in the volatile liquid vehicle, and moisture-resistant. The presence of free behenic acid increases the moisture-resistant properties of the sheet. The salt, with or without the free acid, is produced in the desired physical form aad chemical purity without dicul-ty and at reasonable cost. Silver stearato has been successfully substituted for silver behenate, and silver salts of 'many other organic 'acids have also been found useful in these heat-sensitive compositions and copying-papers. A partial list of such organic acids includes oleic, lauric, hydroxystearic, acetic, phthalic, terephthalic, butyric, rn-nit-robenzoic, salicylic, phcnylacetic, pyromellitic, p-phenylbenzoic, undecylenic, camphoric, furoic, acetamidobenzoic and o-aminobenzoic.
Reducing agents which have been found useful with such compounds in the formulation of heat-sensitive copy.- sheets include: pyrogallol; 4-azeloyl-'bis-pyrogallol; 4- istearoyl pyrogallol; galloacetophenone; di-tertiary-butyl pyrogallol; gallic acid anilide; methyl gallate, ethyl galllate; normaland iso-propyl gallate; lbutyl gallate; dodecyl gallate; gallic acid; ammonium gallate; ethyl protocatechuate; cetyl protocatechuate; 2,5-dihydroxy benzoic acid, l-hydroxy-Z-naphthoic acid; Z-hydroxy, S-naphthoic acid; phloroglucinol; catechol; 2,3-naphthalene diol; 4- lauroyl catechol; sodium gallate; protocatechualdehyde; 4-methyl esculetin; 3,4-dihydroxy henzoic acid; 2,3-dihydroxy benzoic acid; hydroquinone; 4,4'-dihydroxy biphenyl; 3,4-dihydroxyphenylacetic acid; 4(3',4-dihydroxy phenylazo)benzoic acid; 2,2methylene `bis-3,4,5-trihydroxybenzoic acid; orthoand pana-phenylene diamine; tetramethyl benzidine; 4,4',4diethylamino triphenylmethane; o, m, and p-aminobenzoic acids; alpha and beta naphthols; 4-methoxy, l-hydroxy-dihydronaphthalene; and tetrahydroquinoline. These compounds are cyclic or aromatic `compounds having an active hydrogen atom attached to an atom of carbon, oxygen or nitrogen which in turn is attached to an atom of the cyclic ring. They are capable of causing the reduction of silver ion and precipitation of metallic silver on being dissolved at moderate temperature in la solution of `aqueous silver nitrate in an organic solvent.
The reactant materials are preferably applied to a` thin exible carrier or backing, such as paper or transparent film, in conjunction with a film-forming polymeric or resinous binder. In somewhat larger amounts the binder may itself serve the function of a carrier film; or the reactants may be supported in a fibrous web in the substantial absence of binder. Waxes, fibrous materials, pigments, fillers, dyes, fusible or infusible particulate materials, and various other additives may `be included for special purposes. The metal salt and organic reducing agent are preferably intermixcd prior to coating, but may be applied in separate but contiguous layers if desired, in which case the toning ,agent is present `at least in the metal salt layer.
By means of the electron microscope it has been observed that the size of the metal particles vaygipearing in the heated image areas of copy-sheets las hereinbefore described is significantly increased by the incorporation of the toning agent in the heat-sensitive layer. Again, the silver particles precipitated from silver nitrate solution by addition of an acetone solution of hydroquinone or the like are found to have a dilferent shape and an increased apparent volume when precipitation occurs in the presence of a toning agent. increase in apparent volume of precipitate may also be observed on addition of small amounts of a toning agent to the silver nitrate-hydroquinone mixture after initial precipitation. In possible explanation of these effects as well as of the toning effect generally, it is suggested that silver metal as normally precipitated carries with it adsorbed silver ions; that the toning agents are acidic, or contain labile hydrogen atoms, and permit anion formation; that fusion of one or more of the components of the heat-sensitive coupling permits in effect van ionization of the acidic toning agent along with oxidation-reduction reaction of the maior reactants; that the resulting E anions then neutralize the adsorbed silver ions to permit the growth of particle size', and that the increased size of particles provides for increased internal reliection within the particles, resulting in a darker-appearing image. But regardless of theory, it has been shown that darker and more pleasing image-forming areas are obtainable by incorporation, in heat-sensitive copy-sheets employing metalliberating oxidation-reduction reaction com-positions, of heterocyclic organic toning agents containing at least two hetero atoms of which at least one is a nitrogen atom.
What I claim is as follows:
1. A heat-sensitive chemically reactive copy-sheet suitable for the preparation from diierentially radiationabsorptive graphic originals of thermographic reproductions having dark-colored image areas of pleasing appearance, said copy-sheet comprising a thin iiexible carrier web coated with a visibly heat-sensitive coating comprising (l) a lmJforrning binder, (2) a noble metal salt of -an organic acid, an-d (3) a cyclic organic reducing agent for the noble metal ions, having an active hydrogen atom attached to an atom which is selected from the class of oxygen, nitrogen and carbon atoms and is directly attached to an atom of the cyclic ring, and additionally including (4) va significant small proportion, suicient to cause observable darkening of the therrnographic image, of phthalazinone.
2. A heat-sensitive chemically reactive copy-sheet suitable for the preparati-on, from differenti-ally radiationabsorptive graphic originals, of thermographic reproductions having dense black to blue-black image areas, said copy-sheet including a visibly heat-sensitive layer comprising a chemically reactive heat-sensitive mixture of a silver salt of an organic acid and an organic reducing agent for the silver ions, and phthalazinone in a small amount suicient to cause observable darkening of the thermographic image.
References Cited in the file of this patent UNITED STATES PATENTS 2,514,650 Knott et al. July l1, 1950 2,699,393 Weyde r Ian. 11, 1955 2,910,377 Owen Oct. 27, 1959
Claims (1)
1. A HEAT-SENSITIVE CHEMICALLY REACTIVE COPY-SHEET SUITABLE FOR THE PREPARATION FROM DIFFERENTLY RADIATIONABSORPTIVE GRAPHIC ORIGINALS OF THERMOGRAPHIC REPRODUCTIONS HAVING DARK-COLORED IMAGE AREAS OF PLEASING APPEARANCE, SAID COPY-SHEET COMPRISING A THIN FLEXIBLE CARRIER WEB COATED WITH A VISIBLY HEAT-SENSITIVE COATING COMPRISING (1) A FILM-FORMING BINDER, (2) A NOBLE METAL SALT OF AN ORGANIC ACID, AND (3) A CYCLIC ORGANIC REDUCING AGENT FOR THE NOBLE METAL IRONS, HAVING AN ACTIVE HYDROGEN ATOM ATTACHED TO AN ATOM WHICH IS SELECTED FROM THE CLASS OF OXYGEN, NITROGEN AND CARBON ATOMS AND IS DIRECTLY ATTACHED TO AN ATOM OF THE CYCLIC RING, AND ADDITIONALLY INCLUDING (4) A SIGNIFICANT SMALL PROPORTION, SUFFICIENT TO CAUSE OBSERVABLE DARKENING OF THE THERMOGRAPHIC IMAGE OF PHTHALAZINONE.
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US84854959 US3080254A (en) | 1959-10-26 | 1959-10-26 | Heat-sensitive copying-paper |
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US84854959 US3080254A (en) | 1959-10-26 | 1959-10-26 | Heat-sensitive copying-paper |
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US3342618A (en) * | 1962-12-31 | 1967-09-19 | Ibm | Thermographic copying material |
US3446648A (en) * | 1965-09-27 | 1969-05-27 | Minnesota Mining & Mfg | Reactive copying sheet and method of using |
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US3515559A (en) * | 1966-09-30 | 1970-06-02 | Minnesota Mining & Mfg | Dry process proof sheet composition |
US3816139A (en) * | 1970-04-13 | 1974-06-11 | Nashua Corp | Thermographic copy sheet containing phthalimide |
US3839041A (en) * | 1970-06-03 | 1974-10-01 | Eastman Kodak Co | Stabilizer precursors in photothermographic elements and compositions |
US3844797A (en) * | 1972-04-27 | 1974-10-29 | Agfa Gevaert | Photosensitive recording material |
US3847612A (en) * | 1973-02-02 | 1974-11-12 | Minnesota Mining & Mfg | Light-sensitive heat-developable sheet material |
US3885967A (en) * | 1973-05-07 | 1975-05-27 | Fuji Photo Film Co Ltd | Thermally developable light-sensitive element |
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 |
US4076534A (en) * | 1973-10-16 | 1978-02-28 | Fuji Photo Film Co., Ltd. | Heat developable light-sensitive material |
US4268626A (en) * | 1978-08-28 | 1981-05-19 | Asahi Kasei Kogyo Kabushiki Kaisha | Dry image forming material |
US4349623A (en) * | 1979-06-15 | 1982-09-14 | Fuji Photo Film Co., Ltd. | Silver halide photographic materials |
US4379835A (en) * | 1980-12-22 | 1983-04-12 | Minnesota Mining And Manufacturing Company | Black image from a thermographic imaging system |
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US5529889A (en) * | 1992-03-02 | 1996-06-25 | Canon Kabushiki Kaisha | Heat developable photosensitive material and image forming method which uses the same |
US5541055A (en) * | 1993-09-28 | 1996-07-30 | Canon Kabushiki Kaisha | Heat developing photosensitive material and image formed by using the same |
US5547831A (en) * | 1992-11-18 | 1996-08-20 | Canon Kabushiki Kaisha | Dry process silver salt photosensitive material and image forming method making use of this dry process silver salt photosensitive material |
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