EP0122468B1 - Wärmeempfindliches Aufzeichnungsblatt - Google Patents
Wärmeempfindliches Aufzeichnungsblatt Download PDFInfo
- Publication number
- EP0122468B1 EP0122468B1 EP84102807A EP84102807A EP0122468B1 EP 0122468 B1 EP0122468 B1 EP 0122468B1 EP 84102807 A EP84102807 A EP 84102807A EP 84102807 A EP84102807 A EP 84102807A EP 0122468 B1 EP0122468 B1 EP 0122468B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- phthalic acid
- sensitive recording
- heat
- recording sheet
- heat sensitive
- 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
Links
- 239000011888 foil Substances 0.000 title 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 44
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- XIKIUQUXDNHBFR-UHFFFAOYSA-N monobenzyl phthalate Chemical group OC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 XIKIUQUXDNHBFR-UHFFFAOYSA-N 0.000 claims description 3
- SOMMOMFRWWYPHK-UHFFFAOYSA-N 2-(4-ethylphenoxy)carbonylbenzoic acid Chemical compound C1=CC(CC)=CC=C1OC(=O)C1=CC=CC=C1C(O)=O SOMMOMFRWWYPHK-UHFFFAOYSA-N 0.000 claims description 2
- GOVBKFNXUNXORO-UHFFFAOYSA-N 2-(4-methylphenoxy)carbonylbenzoic acid Chemical compound C1=CC(C)=CC=C1OC(=O)C1=CC=CC=C1C(O)=O GOVBKFNXUNXORO-UHFFFAOYSA-N 0.000 claims description 2
- MXOGJBKTZBIWOT-UHFFFAOYSA-N 2-phenoxycarbonylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OC1=CC=CC=C1 MXOGJBKTZBIWOT-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- -1 sensitizer Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- 238000005755 formation reaction Methods 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- RYHQDYUGPBZCFQ-UHFFFAOYSA-N 2'-anilino-3'-methyl-6'-piperidin-1-ylspiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound CC1=CC=2OC3=CC(N4CCCCC4)=CC=C3C3(C4=CC=CC=C4C(=O)O3)C=2C=C1NC1=CC=CC=C1 RYHQDYUGPBZCFQ-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 1
- JFNWGAYGVJGNBG-UHFFFAOYSA-N 2'-anilino-3'-methyl-6'-pyrrolidin-1-ylspiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound CC1=CC=2OC3=CC(N4CCCC4)=CC=C3C3(C4=CC=CC=C4C(=O)O3)C=2C=C1NC1=CC=CC=C1 JFNWGAYGVJGNBG-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- KECCFSZFXLAGJS-UHFFFAOYSA-N 4-methylsulfonylphenol Chemical compound CS(=O)(=O)C1=CC=C(O)C=C1 KECCFSZFXLAGJS-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- RCVMSMLWRJESQC-UHFFFAOYSA-N 7-[4-(diethylamino)-2-ethoxyphenyl]-7-(1-ethyl-2-methylindol-3-yl)furo[3,4-b]pyridin-5-one Chemical compound CCOC1=CC(N(CC)CC)=CC=C1C1(C=2C3=CC=CC=C3N(CC)C=2C)C2=NC=CC=C2C(=O)O1 RCVMSMLWRJESQC-UHFFFAOYSA-N 0.000 description 1
- 241001295925 Gegenes Species 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
- KASSDEATXUCRAV-UHFFFAOYSA-N butyl 4-hydroxybenzenesulfonate Chemical compound CCCCOS(=O)(=O)C1=CC=C(O)C=C1 KASSDEATXUCRAV-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000000332 coumarinyl group Chemical class O1C(=O)C(=CC2=CC=CC=C12)* 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical class 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000011160 magnesium carbonates Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000001454 recorded image Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/333—Colour developing components therefor, e.g. acidic compounds
- B41M5/3333—Non-macromolecular compounds
- B41M5/3335—Compounds containing phenolic or carboxylic acid groups or metal salts thereof
Definitions
- the invention relates to a heat-sensitive recording sheet which has a high degree of whiteness, which is retained better than before even over a long period of time.
- a heat-sensitive recording sheet is generally obtained by placing it on the surface of a support, e.g. B. a paper or film, etc., a coating composition which is obtained by finely grinding and dispersing a colorless chromogenic substance and a color developing material, e.g. B. a phenolic substance, mixing the dispersions obtained and adding a binder, filler, sensitizer, lubricant and other auxiliaries has been obtained.
- a support e.g. B. a paper or film, etc.
- a coating composition which is obtained by finely grinding and dispersing a colorless chromogenic substance and a color developing material, e.g. B. a phenolic substance, mixing the dispersions obtained and adding a binder, filler, sensitizer, lubricant and other auxiliaries has been obtained.
- the coating When exposed to heat or heat, the coating immediately undergoes a chemical reaction in which a color is formed. Depending on the choice of special, colorless chromogenic substances, various clear colors can be created.
- the heat-sensitive recording sheet should still have sufficient color-forming sensitivity for bright recordings with little heat input from the thermal head.
- a particularly effective and preferred phenol is 4,4'-isopropylidenediphenol (bisphenol A) which is now commonly used, inter alia because of its stability, low cost, availability in trade, etc.
- 4,4'-isopropylidenediphenol has the disadvantage that it requires a higher color formation temperature. It is therefore not well suited for recordings in which the amount of heat supplied is small and difficulties such as sticking to the thermal head, etc. can easily arise.
- the color formation temperature of a heat-sensitive sheet must be such that the colorless chromogenic dye or an organic acid such as a phenol is melted or liquid due to the application of heat. If both color forming materials have higher melting points, a substance with a lower melting point is added. The color formation reaction can occur at a lower temperature if one of the farting materials is dissolved due to the melting of this substance.
- heat-fusible substances with a low melting point e.g. B. various waxes, fatty acid amides, alkylated bisphenols, substituted biphenylalkanes, coumarin compounds or diphenylamines, as sensitizers or melting point depressants.
- the color formation reaction can only take place when the sensitizer has melted, so that a thermal response sufficient for rapid dynamic recording to the small amount of heat delivered in short time pulses cannot be achieved.
- the invention is therefore based on the object of providing a heat-sensitive recording sheet which, because of its advantageous thermal responsiveness, enables intensive, clear, high-density recording with rapid recording.
- the heat-sensitive recording sheet is said to have a high degree of whiteness, which is retained better over a longer period than before.
- the heat-sensitive recording sheet is said to provide an excellent copy paper for a thermal copying machine of the infrared or strobe type when coated on a thin base paper or a film.
- the coating amount should be reduced and the productivity should be increased in the production thereof.
- a heat-sensitive recording sheet which contains a phthalic acid monoester of the general formula as a color developing agent in the color formation layer in the R for -C 6 H 5 , -CH 2 is where X is alkyl, halogen or alkoxy.
- Color developing agents used to date are phenolic substances such as bisphenol A, p-hydroxybenzoic acid ester, etc.
- organic carboxylic acids are also described in Japanese Patent Publication 4160/1968, Japanese Patent Laid-Open 39139/1978, etc., but they are described because of the insufficient color developing ability and unstable background whiteness not used in practice.
- FR-A-2 243 830 describes heat-sensitive recording sheets which contain, in addition to conventional additives, a colorless or slightly colored chromogenic dye in the color formation layer and a phthalic acid monoester as color developing agent.
- phthalic acid monoesters can include cycloalkyl esters or alkyl esters with at least 4 carbon atoms, the alkyl esters in the alkyl part being unsubstituted or substituted with oxygen functions, such as a hydroxyl, etherified hydroxy or acyloxy group.
- the phthalic acid monoesters according to the invention have a much better color development capacity and a considerably more stable degree of whiteness of the background than the known organic carboxylic acids.
- Typical examples of the phthalic acid monoesters according to the invention are phthalic acid monophenyl ester, phthalic acid monobenzyl ester, phthalic acid monomethylphenyl ester, phthalic acid monoethylphenyl ester, phthalic acid monoalkylbenzyl ester, phthalic acid monohalobenzyl ester, phthalic acid monoalkoxybenzyl ester, etc.
- the phthalic acid monoesters used in the invention can be used alone or in a mixture with organic acids or phenols, such as bisphenol A (4,4'-isopropylidenediphenol), p, p '- (1-methyl-n-hexylidene) diphenol, p-tertiary butylphenol, p-phenylphenol, p-hydroxylbenzoic acid ester, novolactypphenol resin, 4-hydroxy-1-methylsulfonylbenzene, 4-hydroxy-1-butyloxysulfonylbenzene, etc. can be used.
- organic acids or phenols such as bisphenol A (4,4'-isopropylidenediphenol), p, p '- (1-methyl-n-hexylidene) diphenol, p-tertiary butylphenol, p-phenylphenol, p-hydroxylbenzoic acid ester, novolactypphenol resin, 4-hydroxy-1-methylsulfonylbenzene
- the amount of the phthalic acid monoesters according to the invention and the type and amount of the other constituents which are chosen depending on the desired effect and the suitability for recording purposes are not particularly limited.
- phthalic acid monoester 1-20 parts by weight of a filler per 1 part by weight of the chromogenic dye and 10-20% by weight, based on the total solids content, of a binder.
- Dispersions A and B were separately ground to a particle size of 3 ⁇ m by a ball mill, and then mixed together in the following ratio to produce the heat-sensitive coating colors.
- working examples 1-a to 1-d according to the invention give a recording sheet with a good whiteness and a less reduction in time compared to the sheet according to comparative experiment 1-e in which bisphenol A was used.
- the exemplary embodiments according to the invention result in a highly dynamic image density during rapid recording with a facsimile machine.
- phthalic acid monobenzyl ester has exceptional effects.
- the dispersions were ground separately into a dispersion by means of an attritor until the particle size was 3 1 1 m. The dispersions were then mixed together in the ratio described below to produce heat sensitive coating colors.
- Heat-sensitive recording sheets were produced as in Example 1.
- the heat-sensitive recording sheet of the present invention gives a high whiteness of the background and good durability at high humidity compared to the sheet of Comparative Experiment 2 in which bisphenol A was used together with a sensitizer.
- the heat-sensitive recording sheet according to the invention has an astonishingly high image density when recorded quickly with a facsimile machine in comparison with the sheet of comparative experiment 2.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58041436A JPS59167294A (ja) | 1983-03-15 | 1983-03-15 | 感熱記録シ−ト |
JP41436/83 | 1983-03-15 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0122468A2 EP0122468A2 (de) | 1984-10-24 |
EP0122468A3 EP0122468A3 (en) | 1984-12-27 |
EP0122468B1 true EP0122468B1 (de) | 1987-07-01 |
Family
ID=12608317
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP84102807A Expired EP0122468B1 (de) | 1983-03-15 | 1984-03-14 | Wärmeempfindliches Aufzeichnungsblatt |
Country Status (4)
Country | Link |
---|---|
US (1) | US4498091A (enrdf_load_stackoverflow) |
EP (1) | EP0122468B1 (enrdf_load_stackoverflow) |
JP (1) | JPS59167294A (enrdf_load_stackoverflow) |
DE (1) | DE3464474D1 (enrdf_load_stackoverflow) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6046293A (ja) * | 1983-08-24 | 1985-03-13 | Jujo Paper Co Ltd | 感熱記録紙 |
JPS60122191A (ja) * | 1983-12-06 | 1985-06-29 | Ricoh Co Ltd | 感熱記録材料 |
JPS62148288A (ja) * | 1985-12-24 | 1987-07-02 | Kanzaki Paper Mfg Co Ltd | 感熱記録体 |
JPS6317081A (ja) * | 1986-07-10 | 1988-01-25 | Kanzaki Paper Mfg Co Ltd | 感熱記録体 |
EP0608579B1 (en) * | 1993-01-29 | 1997-04-16 | Agfa-Gevaert N.V. | A heat and light sensitive imaging element |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3911171A (en) * | 1973-09-14 | 1975-10-07 | Agfa Gevaert A Naamloze Vennoo | Thermographic recording process |
US3965282A (en) * | 1973-09-14 | 1976-06-22 | Agfa-Gevaert N.V. | Thermographic recording material |
-
1983
- 1983-03-15 JP JP58041436A patent/JPS59167294A/ja active Granted
-
1984
- 1984-03-14 DE DE8484102807T patent/DE3464474D1/de not_active Expired
- 1984-03-14 EP EP84102807A patent/EP0122468B1/de not_active Expired
- 1984-03-15 US US06/590,199 patent/US4498091A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US4498091A (en) | 1985-02-05 |
EP0122468A2 (de) | 1984-10-24 |
EP0122468A3 (en) | 1984-12-27 |
DE3464474D1 (en) | 1987-08-06 |
JPH0211439B2 (enrdf_load_stackoverflow) | 1990-03-14 |
JPS59167294A (ja) | 1984-09-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE3114681C2 (de) | "Wärmeempfindliches Aufzeichnungsblatt" | |
EP0211263B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP0171810B1 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
DE3540627C2 (enrdf_load_stackoverflow) | ||
EP0307836B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
DE3331078C2 (de) | Wärmeempfindliches Aufzeichnungsblatt und Verfahren zu dessen Herstellung | |
DE3801837A1 (de) | Waermeempfindliche aufzeichnungsmaterialien | |
EP0251209B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP0248405B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP0287121B1 (de) | Wärme- und lichtempfindliches Aufzeichnungsmaterial und Aufzeichnungsverfahren | |
EP0122468B1 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
EP0173232A2 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
EP0058345B2 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
EP0181646A2 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
EP0286116B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP0224075B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
DE4026866A1 (de) | Hitzeempfindliches aufzeichnungsmedium | |
DE3414297C2 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP0137982B1 (de) | Wärmeempfindliches Aufzeinungsblatt | |
EP0066813B1 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
EP0422680B1 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
EP0135901B1 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
DE3342149A1 (de) | Waermeempfindliches aufzeichnungsblatt | |
EP0421278B1 (de) | Wärmeempfindliches Aufzeichnungsblatt | |
DE69415382T2 (de) | Wärmeempfindliches Aufzeichnungsmaterial |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Designated state(s): BE DE FR GB |
|
AK | Designated contracting states |
Designated state(s): BE DE FR GB |
|
17P | Request for examination filed |
Effective date: 19850128 |
|
17Q | First examination report despatched |
Effective date: 19860306 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): BE DE FR GB |
|
REF | Corresponds to: |
Ref document number: 3464474 Country of ref document: DE Date of ref document: 19870806 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
REG | Reference to a national code |
Ref country code: FR Ref legal event code: CD |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19950306 Year of fee payment: 12 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19950309 Year of fee payment: 12 Ref country code: DE Payment date: 19950309 Year of fee payment: 12 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19950428 Year of fee payment: 12 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19960314 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Effective date: 19960331 |
|
BERE | Be: lapsed |
Owner name: NIPPON PAPER INDUSTRIES CO. LTD Effective date: 19960331 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19960314 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19961129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19961203 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |