JPH0549476B2 - - Google Patents
Info
- Publication number
- JPH0549476B2 JPH0549476B2 JP63304284A JP30428488A JPH0549476B2 JP H0549476 B2 JPH0549476 B2 JP H0549476B2 JP 63304284 A JP63304284 A JP 63304284A JP 30428488 A JP30428488 A JP 30428488A JP H0549476 B2 JPH0549476 B2 JP H0549476B2
- Authority
- JP
- Japan
- Prior art keywords
- transfer
- coating layer
- transfer tape
- plastic
- tape according
- 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
- 238000012546 transfer Methods 0.000 claims description 107
- 239000011247 coating layer Substances 0.000 claims description 60
- 238000000576 coating method Methods 0.000 claims description 27
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 26
- 229920003023 plastic Polymers 0.000 claims description 26
- 239000004033 plastic Substances 0.000 claims description 26
- 239000011248 coating agent Substances 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 22
- 239000003086 colorant Substances 0.000 claims description 19
- 239000000049 pigment Substances 0.000 claims description 18
- 239000006185 dispersion Substances 0.000 claims description 15
- 229920002678 cellulose Polymers 0.000 claims description 14
- 239000001913 cellulose Substances 0.000 claims description 13
- 239000011230 binding agent Substances 0.000 claims description 7
- 238000012937 correction Methods 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 229920002635 polyurethane Polymers 0.000 claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000001856 Ethyl cellulose Substances 0.000 claims description 5
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical group CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 5
- 229920001249 ethyl cellulose Polymers 0.000 claims description 5
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000000975 dye Substances 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- 239000012463 white pigment Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 239000000981 basic dye Substances 0.000 claims description 2
- 239000007850 fluorescent dye Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 11
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- -1 polyethylene terephthalate Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 239000004014 plasticizer Substances 0.000 description 5
- 235000010215 titanium dioxide Nutrition 0.000 description 5
- 229910000323 aluminium silicate Inorganic materials 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000012831 Printan Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical group CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000004815 dispersion polymer Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000004447 silicone coating Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 229920001864 tannin Polymers 0.000 description 2
- 239000001648 tannin Substances 0.000 description 2
- 235000018553 tannin Nutrition 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000896 Ethulose Polymers 0.000 description 1
- 239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- AOADSHDCARXSGL-ZMIIQOOPSA-M alkali blue 4B Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC2=CC=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C2=CC=CC=C2)=CC=C1N.[Na+] AOADSHDCARXSGL-ZMIIQOOPSA-M 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 230000000181 anti-adherent effect Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001761 ethyl methyl cellulose Substances 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical class OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- WGPCGCOKHWGKJJ-UHFFFAOYSA-N sulfanylidenezinc Chemical compound [Zn]=S WGPCGCOKHWGKJJ-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
- B41M5/025—Duplicating or marking methods; Sheet materials for use therein by transferring ink from the master sheet
- B41M5/03—Duplicating or marking methods; Sheet materials for use therein by transferring ink from the master sheet by pressure
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65H—HANDLING THIN OR FILAMENTARY MATERIAL, e.g. SHEETS, WEBS, CABLES
- B65H37/00—Article or web delivery apparatus incorporating devices for performing specified auxiliary operations
- B65H37/002—Web delivery apparatus, the web serving as support for articles, material or another web
- B65H37/005—Hand-held apparatus
- B65H37/007—Applicators for applying coatings, e.g. correction, colour or adhesive coatings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J29/00—Details of, or accessories for, typewriters or selective printing mechanisms not otherwise provided for
- B41J29/26—Devices, non-fluid media or methods for cancelling, correcting errors, underscoring or ruling
- B41J29/36—Devices, non-fluid media or methods for cancelling, correcting errors, underscoring or ruling for cancelling or correcting errors by overprinting
- B41J29/367—Devices, non-fluid media or methods for cancelling, correcting errors, underscoring or ruling for cancelling or correcting errors by overprinting sheet media carrying a pigmented transferable correction layer
-
- 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
- B41M5/10—Duplicating or marking methods; Sheet materials for use therein by using carbon paper or the like
-
- 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
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M2205/00—Printing methods or features related to printing methods; Location or type of the layers
- B41M2205/16—Correction processes or materials
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Decoration By Transfer Pictures (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Laminated Bodies (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
産業上の利用分野:
本発明は、支持材と圧感接着被膜とを有し、支
持材と圧感接着被膜との間に、プラスチツク結合
転写被覆層が配置され、プラスチツク結合転写被
覆層は圧感接着被膜に対し、支持材に対するより
強い接着力を有する修正およびマーキング用の可
撓性多層転写テープに関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application: The present invention comprises a support material and a pressure sensitive adhesive coating, a plastic bond transfer coating layer is disposed between the support material and the pressure sensitive adhesive coating, and a plastic bond transfer coating layer is disposed between the support material and the pressure sensitive adhesive coating. Transfer coating layers relate to flexible multilayer transfer tapes for correction and marking with stronger adhesion to the support as opposed to pressure-sensitive adhesive coatings.
従来の技術:
顔料を含む液体系を、ミスタイプした表示を隠
蔽するために使用する多数の方法が公知である。
事務所では揮発性の高い有機溶剤を含む白色顔料
分散液が、タイプした文字等の修正のためブラシ
で適用される。しかし、高揮発性有機溶剤の蒸発
は環境に有害である。蒸発が終了し、修正タイプ
が可能になるまで比較的長時間待つことが必要で
ある。ブラシによる修正分散液の適用によれば一
般に均一な被覆層は得られない。Prior Art: A number of methods are known in which liquid systems containing pigments are used to conceal mistyped indicia.
In the office, a white pigment dispersion containing a highly volatile organic solvent is applied with a brush to correct typed text, etc. However, evaporation of highly volatile organic solvents is harmful to the environment. It is necessary to wait for a relatively long time until the evaporation is finished and modification types are possible. Application of the modified dispersion by brush generally does not result in a uniform coating.
比較的良好な修正は、多層の可撓性転写シート
を記載したドイツ国特許出願公開第2626891号明
細書により可能となり、この多層シートは接着性
分離層で被覆された可撓性支持材、ポリビニルア
ルコール結合した転写層および薄い接着被膜から
なる。転写層は顔料としてチタン白をも含有す
る。支持材を除去した後、転写層はミスタイプし
た文字の修正被膜として役立つ。下記に本発明と
関連して説明するようなハンド転写ロールでの使
用は記載されておらず、試験で判明したように、
修正被膜の所望のすつきりとした剥離は得られな
い。 A relatively good modification is made possible by DE 26 26 891, which describes a multilayer flexible transfer sheet, which consists of a flexible support coated with an adhesive separation layer, polyvinyl Consists of an alcohol-bonded transfer layer and a thin adhesive coat. The transfer layer also contains titanium white as pigment. After removing the support, the transfer layer serves as a correction coating for mistyped characters. It is not described for use with hand transfer rolls as described below in connection with the present invention and, as found in testing,
The desired smooth release of the correction coating cannot be achieved.
発明が解決しようとする課題:
本発明の課題は、前記の修正およびマーキング
用の転写テープを、プラスチツク結合転写被覆層
を隠蔽すべき個所にきれいにかつくつきりと適用
することができ、かつ手動器具の使用によつても
紙へ簡単、迅速かつ均一に適用しうるようにさら
に改善することである。OBJECT OF THE INVENTION It is an object of the present invention to be able to apply the correction and marking transfer tape neatly and firmly to the areas where the plastic-bonded transfer coating layer is to be hidden, and without using manual tools. Another object of the present invention is to further improve the ease, speed and uniformity of application to paper by the use of .
課題を解決するための手段:
この課題は、本発明により、プラスチツク結合
転写被覆層が可溶性セルロース誘導体を含有し、
該誘導体は転写被覆層中に約0.5〜5重量%の量
で存在することによつて解決される。Means for Solving the Problem: This problem is achieved by the present invention, wherein the plastic-bonded transfer coating layer contains a soluble cellulose derivative;
The derivative is present in the transfer coating layer in an amount of about 0.5 to 5% by weight.
本発明による可撓性の転写テープの支持材は、
望ましくはタイプライターリボンの支持材と関連
して使用されるようなプラスチツクフイルム、た
とえばポリエチレンテレフタラート、ポリプロピ
レン、ポリエチレン、ポリ塩化ビニルおよびポリ
カーボネートからなる。シリコーン塗被紙も支持
材として適当である。シリコーン被膜は、プラス
チツク結合転写被覆層と支持材との間の付着力を
減少する。シリコーン被膜の代わりに、種々の粘
着防止剤、たとえばポリテトラフルオロエチレン
を使用することもできる。 The flexible transfer tape support according to the invention comprises:
It preferably comprises plastic films such as those used in connection with typewriter ribbon supports, such as polyethylene terephthalate, polypropylene, polyethylene, polyvinyl chloride and polycarbonate. Silicone coated papers are also suitable as supports. The silicone coating reduces adhesion between the plastic bonded transfer coating layer and the support. Instead of silicone coatings, various antiblocking agents can also be used, such as polytetrafluoroethylene.
作用:
支持材の厚さは望ましくは約10〜60μmとくに
約15〜55μmであり、プラスチツク結合被覆層は
約5〜40μm、とくに約15〜25μmの厚さを有し、
圧感接着被膜の厚さは約1〜8μm、とくに約2
〜5μmである。本発明の転写テープを最適にす
るため、圧感接着被膜と転写被覆層の厚さの比を
約1:4〜1:12とくに約1:8〜1:10に選ぶ
のが適当である。Effect: The thickness of the support material is preferably about 10 to 60 μm, especially about 15 to 55 μm, the plastic bonding layer has a thickness of about 5 to 40 μm, especially about 15 to 25 μm,
The thickness of the pressure-sensitive adhesive film is about 1 to 8 μm, especially about 2 μm.
~5μm. In order to optimize the transfer tape according to the invention, it is suitable to choose a thickness ratio of pressure-sensitive adhesive coating and transfer coating layer of about 1:4 to 1:12, in particular about 1:8 to 1:10.
圧感接着被膜は、市販の圧感接着剤からなつて
いてもよい。これらは高い接着力を有する弾性的
かつ永久接着性の粘着物を形成し、外界温度で限
定圧力下に種々の表面に即時に接着する材料であ
る。これらは、有利には支持材上にすでに配置さ
れている転写被覆層に水溶液の形で適用される。
それというのもこうすればすでに形成したプラス
チツク結合転写被覆層は再び溶解しないからであ
る。このタイプの圧感接着剤のうちアクリレート
系のものがとくに有利である。出発材料はゴム、
ポリアクリレート、ポリビニルエーテルまたはポ
リビニルイソブチレン系の粘性溶液または分散液
である。ポリアクリレート系材料が有利である。
適当な市販製品は、Ucecryl 913Rおよび
Ucecryl PC80(ベルギー国、Ammelicht在、
UCB社から市販)ならびにプラスチツク分散液
VP859/6(Freihoff社から市販)である。望ま
しくは、通常水性媒体中に存在する適用すべき圧
感接着剤は湿潤剤または表面活性剤(Byk Wの
商標で市販)を含有する。圧感接着被膜を形成す
るための圧感接着剤の前記溶液または分散液は、
とくに約1〜5g/m2、有利には約2〜4g/m2
の量で転写被覆層に適用される。 The pressure sensitive adhesive coating may consist of a commercially available pressure sensitive adhesive. These are materials that form elastic, permanently adhesive adhesives with high adhesive strength and adhere instantly to various surfaces under limited pressure at ambient temperatures. These are preferably applied in the form of an aqueous solution to the transfer coating layer already arranged on the support.
This is because in this way the already formed plastic-bonded transfer coating layer does not dissolve again. Of this type of pressure-sensitive adhesives, those based on acrylates are particularly advantageous. The starting material is rubber,
Viscous solutions or dispersions based on polyacrylate, polyvinyl ether or polyvinyl isobutylene. Polyacrylate materials are preferred.
Suitable commercially available products include Ucecryl 913R and
Ucecryl PC80 (located in Ammericht, Belgium)
commercially available from UCB) and plastic dispersions
VP859/6 (commercially available from Freihoff). Desirably, the pressure-sensitive adhesive to be applied, which is usually present in an aqueous medium, contains a wetting agent or a surfactant (sold under the trademark Byk W). The solution or dispersion of a pressure-sensitive adhesive for forming a pressure-sensitive adhesive coating comprises:
In particular about 1 to 5 g/m 2 , advantageously about 2 to 4 g/m 2
is applied to the transfer coating layer in an amount of .
プラスチツク結合転写被覆層を形成するのに
は、熱可塑性または熱弾性ポリマーを溶液または
分散液の形で使用するのが望ましい。本発明の範
囲内では次の物質が課題解決のため有利に使用さ
れる:
(a) 分子量15000〜50000のポリウレタン、たとえ
ばStahl−ChemieのPermuthane U4924または
Bayer社のDesmolac2100、
(b) 分子量20000〜30000の線状飽和ポリエステ
ル、たとえばGoodyear Tire&Rubber社の
Vitel PE 307、
(c) スチレン−イソプレン−スチレンコーポリマ
ー、たとえばShell−Chemie社のCariflexTR
1107、
(d) アクリレートおよびメタクリレート、たとえ
ばRo¨hm社のPexigum7H、
(e) ジフエニルカルボン酸変性ポリアミド、たと
えばRhone−Poulenc社の Scope30または
Emery Chemicals社のEmerez 1533、
(f) ビニルプロピオネート系ポリマー分散液、た
とえばBASF社のPropiofan 6D、
(g) カルボキシメチル基含有水溶性ポリメタクリ
レート、たとえばRo¨hm社のRohagit SD15。 Preferably, the thermoplastic or thermoelastic polymer is used in the form of a solution or dispersion to form the plastic bond transfer coating layer. Within the scope of the invention, the following substances are advantageously used for solving the problem: (a) Polyurethanes with a molecular weight of 15,000 to 50,000, such as Permuthane U4924 from Stahl-Chemie or
Desmolac 2100 from Bayer; (b) Linear saturated polyesters with molecular weights between 20,000 and 30,000, such as from Goodyear Tire & Rubber.
Vitel PE 307, (c) Styrene-isoprene-styrene copolymers, such as Shell-Chemie's CariflexTR
1107, (d) acrylates and methacrylates, such as Pexigum 7H from Ro¨hm, (e) diphenylcarboxylic acid-modified polyamides, such as Scope 30 from Rhone-Poulenc or
Emerez 1533 from Emery Chemicals, (f) Vinylpropionate polymer dispersions, such as Propiofan 6D from BASF, (g) Water-soluble polymethacrylates containing carboxymethyl groups, such as Rohagit SD15 from Ro¨hm.
このリストは完全とは云えず、かつ選択に関し
ての制限でもない。とくにバインダプラスチツク
の性質が本発明の要旨を形成しないので、他のバ
インダが使用可能であることは当業者には容易に
明らかである。 This list is neither complete nor limiting in terms of selection. It will be readily apparent to those skilled in the art that other binders can be used, particularly as the nature of the binder plastic does not form the subject matter of the invention.
本発明の最適の実施形を達成するため、転写被
覆層を形成するためのバインダプラスチツクを選
択する際、使用する可塑剤の性質を考慮に入れな
ければならない。可塑剤は、転写被覆層を修正ま
たは隠蔽すべき表面へ適用する際、一般には薄い
圧感接着被膜に浸透せず、修正すべき個所または
そこに施された着色剤と接触せず、かつ着色剤を
不所望に溶解して転写被覆層の変色を伴うことの
ないものを使用しなければならない。シリコー
ン、ヒマシ油および鉱油のような通常の可塑剤が
適当なことが明らかになつた。他の分野で有利に
使用される他の可塑剤、たとえばフタレートおよ
びオレイルアルコールは不適当である。例外的な
場合、可塑剤の不利な効果を防止するため、プラ
スチツク結合転写被覆層にいわゆる“レーキ”を
添加することができる。レーキは移行する着色剤
を沈殿させ、または不溶性にするので、着色剤が
適用した転写被覆層へ移行してそれを再着色する
ことがない。適当なレーキはタンニンおよびタン
ニン誘導体である。一般にインキおよびインデイ
アインキの分野で公知のタイプのレーキを使用す
ることができる。レーキはとくにプラスチツク結
合転写被覆層中に約0.5〜5重量%、とくに1.5〜
3.5重量%の量が存在する。約2〜2.5重量%がと
くに有利である。 In order to achieve optimal practice of the invention, the nature of the plasticizer used must be taken into account when selecting a binder plastic for forming the transfer coating layer. When the transfer coating layer is applied to the surface to be modified or concealed, the plasticizer generally does not penetrate the thin pressure-sensitive adhesive coating, does not come into contact with the area to be modified or the colorant applied thereto, and does not interfere with the colorant. It is necessary to use a material that does not cause undesired dissolution and discoloration of the transfer coating layer. Common plasticizers such as silicones, castor oil and mineral oil have proven suitable. Other plasticizers which are used advantageously in other fields, such as phthalates and oleyl alcohol, are unsuitable. In exceptional cases, so-called "lakes" can be added to the plastic bonded transfer coating layer in order to prevent the adverse effects of plasticizers. The lake precipitates or renders the migrating colorant insoluble so that it does not migrate to the applied transfer coating layer and recolor it. Suitable lakes are tannins and tannin derivatives. Lakes of the type generally known in the ink and India ink art can be used. The lake is preferably about 0.5 to 5% by weight, especially 1.5 to 5% by weight, in the plastic bond transfer coating layer.
An amount of 3.5% by weight is present. About 2-2.5% by weight is particularly advantageous.
本発明による転写テープを製造する間、転写被
覆層形成のため選択したバインダプラスチツクは
とくに溶液の形にされ、またはポリマー分散液が
存在する場合分散液として使用される。溶剤の選
択は使用するプラスチツクの性質による。エタノ
ール、イソプロパノールおよびブタノールのよう
なアルコール;アセトンおよびメチルエチルケト
ンのようなケトン;メチル−およびエチルアセテ
ートのようなエステル;トルエンのような芳香族
炭化水素;沸点範囲70〜140℃のベンジンのよう
な脂肪族炭化水素の群からの低沸点または中沸点
有機溶剤を単独または混合物で使用し、ならびに
水を単独で使用するかまたは低沸点水溶性有機溶
剤と混合して使用するのが有利である。溶液また
は分散液中のプラスチツク濃度は、本発明にとり
重要ではない。概略の目安としてのこの濃度は、
約3〜15重量%、とくに約4〜10重量%の範囲で
ある。転写被覆層を形成するため、前記溶液また
は分散液は、支持材へとくに15〜25g/m2、とく
に有利に18〜22g/m2の量で適用される。 During the production of the transfer tape according to the invention, the binder plastic selected for forming the transfer coating layer is preferably in the form of a solution or, if a polymer dispersion is present, used as a dispersion. The choice of solvent will depend on the nature of the plastic used. Alcohols such as ethanol, isopropanol and butanol; ketones such as acetone and methyl ethyl ketone; esters such as methyl- and ethyl acetate; aromatic hydrocarbons such as toluene; aliphatics such as benzine with a boiling point range of 70-140°C It is advantageous to use low-boiling or medium-boiling organic solvents from the group of hydrocarbons, alone or in mixtures, and to use water alone or in admixture with low-boiling water-soluble organic solvents. The concentration of plastic in the solution or dispersion is not critical to the invention. As a rough guide, this concentration is
It ranges from about 3 to 15% by weight, especially from about 4 to 10% by weight. To form the transfer coating layer, the solution or dispersion is applied to the support in an amount of preferably 15 to 25 g/m 2 , particularly preferably 18 to 22 g/m 2 .
本発明における“着色剤”とは、極めて広義の
ものを表わし、染料および顔料を含むすべての色
彩を付与する物質の集合名詞であり、その際顔料
は充てん剤の性質をも有する。染料は不溶性顔料
と異なり水、有機溶剤またはバインダプラスチツ
クに可溶性の着色剤である。着色は直接現れても
よいが、蛍光によつて発現してもよい。蛍光は、
たとえば蛍光発光色の場合に適用される。本発明
の転写テープをタイプした文字、画像表示等の修
正に使用する場合、プラスチツク結合転写被覆層
はとくにチタン白、沈降炭酸カルシウム、アルミ
ナまたはコロイドケイ酸のような白色顔料を含
む。転写被覆層を着色する場合、使用する着色剤
はクロムエロー、オーカー、酸化鉄レツド、コバ
ルトブルー、ウルトラマリンブルー、ベルリンブ
ルーのような無機顔料またはアルカリブルー、フ
タロシアニン、アジ染料、アントラキノノイド、
金属錯体顔料のような有機顔料ならびにカーボン
ブラツクおよび酸化鉄ブラツクである。蛍光染料
の例はDayglo社のBlaze Orange T50、Ciba
Geigy社のMaxilonbrillant Flavin 10 GFF、
Bayer A.G.社のPyraninおよびBASF社の
Basonyl−Rot 540である。 The term "colorant" in the present invention has a very broad meaning and is a collective noun for all color-imparting substances, including dyes and pigments, where the pigments also have filler properties. Dyes are colorants that, unlike insoluble pigments, are soluble in water, organic solvents, or binder plastics. Coloring may appear directly or may be expressed by fluorescence. Fluorescence is
For example, this applies to fluorescent light emission colors. When the transfer tape of the invention is used for modifying typed characters, image displays, etc., the plastic bonded transfer coating layer contains white pigments such as titanium white, precipitated calcium carbonate, alumina or colloidal silicic acid, among others. When coloring the transfer coating layer, the colorants used are inorganic pigments such as chrome yellow, ocher, iron oxide red, cobalt blue, ultramarine blue, Berlin blue, or alkali blue, phthalocyanine, azide dye, anthraquinonoid,
organic pigments such as metal complex pigments and carbon black and iron oxide black. Examples of fluorescent dyes are Dayglo's Blaze Orange T50, Ciba
Geigy's Maxilonbrillant Flavin 10 GFF,
Bayer AG's Pyranin and BASF's
Basonyl-Rot 540.
本発明の転写テープ、とくにプラスチツク結合
転写被覆層の最適の隠蔽力の制御は顔料含有量に
よつて行われる。最適の顔料含有量は選択したバ
インダ、実際の顔料および添加した添加物のよう
な種々のフアクタにより変化するが、とくに臨界
的な値または範囲を記載することはできない。プ
ラスチツク/顔料の比の概略の目安として、約
1:1〜1:12とくに1:3〜1:8さらに有利
には約1:4〜1:7の重量比が示される。 Control of the optimum hiding power of the transfer tapes of the present invention, particularly of the plastic bonded transfer coating layer, is effected by the pigment content. The optimum pigment content will vary depending on various factors such as the binder selected, the actual pigment and any additives added, and no particularly critical value or range can be stated. As a rough guide for the plastic/pigment ratio, a weight ratio of approximately 1:1 to 1:12, in particular 1:3 to 1:8, more preferably approximately 1:4 to 1:7, is indicated.
本発明による転写テープのプラスチツク結合転
写被覆層の主要成分は、剥離助剤としての可溶性
セルロース誘導体である。このような剥離助剤の
使用によつてのみ支持材へ転写被覆層を適用する
際、引張応力条件下にすつきりとした剥離が確実
に達成される。とくに有利なセルロース誘導体
は、有機溶剤および(または)水に可溶のセルロ
ースエーテル、たとえばメチル、エチル、ヒドロ
キシエチル、エチルヒドロキシエチルおよびカル
ボキシメチルセルロース;セルロースエステル、
たとえばセルロースアセテート、アセトブチレー
トおよびプロピオネートである。しかし多数の他
の可溶性セルロース誘導体も適当であり、所望の
効果が得られる。可溶性セルロース誘導体中のセ
ルロース基礎構造が重要であり、エチル基等のよ
うな導入基によりとくに選択された溶剤に可溶性
である誘導体が得られる。 The main component of the plastic-bonded transfer coating layer of the transfer tape according to the invention is a soluble cellulose derivative as a release aid. Only through the use of such a release aid can a clean release be achieved under conditions of tensile stress when applying the transfer coating to the support. Particularly preferred cellulose derivatives are cellulose ethers soluble in organic solvents and/or water, such as methyl, ethyl, hydroxyethyl, ethylhydroxyethyl and carboxymethylcellulose; cellulose esters,
Examples are cellulose acetate, acetobutyrate and propionate. However, many other soluble cellulose derivatives are also suitable and achieve the desired effect. The cellulose basic structure in the soluble cellulose derivatives is important, and introduced groups such as ethyl groups result in derivatives that are soluble in particularly selected solvents.
転写被覆層に添加されるセルロース誘導体の量
は厳密を要せず、プラスチツク、顔料および添加
する他の添加物の性質に依存する。とくに、約
1.5〜3.5重量%の量が有利である。約2〜2.5重量
%の範囲がさらに有利である。これらの値は乾燥
物質に関する。セルロース誘導体とプラスチツク
の量比は、転写被覆層の組成のための基礎として
使用することもできる。概略の目安としてセルロ
ース誘導体とプラスチツクとの比は、約1:2〜
1:20、とくに約1:4〜1:10が挙げられる。 The amount of cellulose derivative added to the transfer coating layer is not critical and depends on the nature of the plastic, pigment and other additives added. In particular, about
Amounts of 1.5 to 3.5% by weight are advantageous. A range of about 2-2.5% by weight is even more advantageous. These values relate to dry matter. The quantity ratio of cellulose derivative to plastic can also be used as a basis for the composition of the transfer coating layer. As a rough guide, the ratio of cellulose derivative to plastic is approximately 1:2 to
1:20, especially about 1:4 to 1:10.
適用法および支持材に適用される転写被覆層の
性質を制御するため、転写被覆層へさらに他の添
加物を加えることができる。これはとくにアルミ
ノケイ酸塩のような隠蔽力改善剤、たとえばカー
ボンブラツクのような着色剤、たとえばCiba
Geigy社のPrintanのような没食子酸誘導体の形
の、とくに塩基性染料の前記レーキである。 Further additives can be added to the transfer coating layer to control the application method and properties of the transfer coating layer applied to the support. This is especially true of hiding power improvers such as aluminosilicates, colorants such as carbon black, e.g. Ciba
Said lakes of basic dyes, especially in the form of gallic acid derivatives, such as Geigy's Printan.
本発明の転写テープの個々の被膜の前記材料
は、一般に圧感接着被膜と転写被覆層との間の付
着張力[ジユプレの式に相当する付着仕事によつ
て定義される(K.L.Wolf“Physik und Chemie
der Grenzfla¨chen”Springer Velag 1957、p164
参照)]が支持材と転写被覆層との間の付着張力
よりも高いという基本的要求を満足する。特殊な
ケースとしてこれが充足されない場合、適当な接
着防止剤をこの基本的要求充足のため支持材へ適
用しなければならない。このような場合、支持材
上に形成される転写被覆層は他の材料、とくに接
触する紙に対し非接着性であるというもう1つの
要求が考慮される。そこで次の付着張力条件によ
り本発明の転写テープを効果的に使用することが
でき、その際記号Sは種々の材料の間の付着張力
比、すなわちS1は紙/圧感接着被膜、S2は転写被
覆層/圧感接着被膜、S3は転写被覆層支持材、S4
は転写被覆層/紙、S5は圧感接着被覆層/支持材
の比を表わし、次の要求が考慮される:S1はS3よ
り高く、S2はS3より高く、S5はS2よりもつと小さ
く、かつS5はS3より小さい。さらに基材、とくに
紙へ適用した転写被覆層の自由表面は外側へ接着
力を有してはならない、すなわちS4はゼロである
か、またはゼロに近い。換言すれば、適用した転
写被覆層は手または紙と接触する際に粘着性であ
つてはならない。 The materials of the individual coatings of the transfer tapes of the invention are generally defined by the adhesion tension between the pressure-sensitive adhesive coating and the transfer coating layer [work of adhesion corresponding to the Giuplet equation (KLWolf “Physik und Chemie
Springer Velag 1957, p164
)] is higher than the adhesion tension between the support material and the transfer coating layer. If, in special cases, this is not fulfilled, a suitable anti-adhesive agent must be applied to the support material in order to fulfill this basic requirement. In such cases, another requirement is taken into account, that the transfer coating formed on the support is non-adhesive to other materials, in particular to the paper with which it comes in contact. The transfer tape of the invention can then be used effectively with the following adhesion tension conditions, where the symbol S is the adhesion tension ratio between the various materials, i.e. S 1 is the paper/pressure-sensitive adhesive coating, S 2 is the adhesion tension ratio between the various materials. Transfer coating layer/pressure-sensitive adhesive coating, S 3 is transfer coating layer support material, S 4
is the ratio of transfer coating layer/paper, S 5 is the ratio of pressure-sensitive adhesive coating layer/support material, the following requirements are taken into account: S 1 is higher than S 3 , S 2 is higher than S 3 , S 5 is higher than S 2 , and S 5 is smaller than S 3 . Furthermore, the free surface of the transfer coating applied to the substrate, in particular paper, must have no outward adhesion, ie S 4 is zero or close to zero. In other words, the applied transfer coating layer should not be tacky on contact with the hand or paper.
本発明の転写テープを製造する有利な方法の特
徴は、前記セルロース誘導体を含有する適当なプ
ラスチツク溶液を、常法、たとえばドクタブレー
ドで可撓性フイルムの形の支持材に適用し、溶剤
を高めた温度で蒸発させ、次に圧感接着剤を含む
水性分散液をドクタブレードまたはロールコータ
のような通常の適用法によつて、形成されたプラ
スチツク結合転写被覆層に適用し、引き続いて水
を蒸発させることである。 A feature of the advantageous process for producing the transfer tapes of the invention is that a suitable plastics solution containing said cellulose derivatives is applied in a customary manner, for example with a doctor blade, to a support in the form of a flexible film, and the solvent is enriched. The aqueous dispersion containing the pressure-sensitive adhesive is then applied to the formed plastic bond transfer coating layer by conventional application methods such as a doctor blade or roll coater, followed by evaporation of the water. It is to let.
本発明による転写テープを使用する場合、圧感
接着剤を備える転写被覆層をロール転写すると同
時に支持材を巻込むことのできる市販のアプリケ
ータを使用するのが有利である。それによつて本
発明の転写テープはとくに容易に扱うことができ
る。アプリケータは、市販の手動器具によつて形
成される。このタイプのとくに適当な器具は、い
わゆるハンドローラであり、転写リボンを巻いた
供給スプールは容易に握りうるケーシング内に配
置され、リボンはケーシングから突出するアプリ
ケータ脚から導出され、この脚からケーシング内
の巻取スプールへ巻戻される。ケーシング内のス
プールの間の適当なギヤにより転写リボンが常に
適当に緊張していることが保証される。転写リボ
ンを使用するために、使用者はケーシングを手に
取り、アプリケータ脚によつて端部エツジ上を通
過する外側の剥離可能の転写被覆層を転写すべき
支持材(たとえば修正を行うためのタイプした紙
シート)に対して圧着する。圧着の間使用者は器
具を基材に対して動かし、それによつてたとえ
ば、隠蔽被覆層または蛍光被覆層が支持材へ転写
され、可撓性支持材は供給スプールから繰出さ
れ、巻取スプールに巻取られる。 When using the transfer tape according to the invention, it is advantageous to use commercially available applicators which are capable of roll-transferring the transfer coating layer with the pressure-sensitive adhesive and simultaneously winding up the support material. The transfer tape according to the invention is thereby particularly easy to handle. The applicator is formed by a commercially available manual instrument. A particularly suitable device of this type is a so-called hand roller, in which a supply spool wrapped with transfer ribbon is arranged in an easily grippable casing, the ribbon being led out from an applicator leg projecting from the casing, and from which the casing It is rewound onto the take-up spool inside. Appropriate gearing between the spools within the casing ensures that the transfer ribbon is properly tensioned at all times. To use a transfer ribbon, the user picks up the casing and attaches the outer peelable transfer coating layer to the support material to be transferred (e.g. for making modifications), which is passed over the end edge by the applicator leg. (typed paper sheet). During crimping, the user moves the instrument relative to the substrate, thereby transferring, for example, an opaque or fluorescent coating layer to the support, and the flexible support being unwound from a supply spool and onto a take-up spool. It is wound up.
本発明の転写テープは、事務所、学校および家
庭で誤つてタイプした文字、マーキング、図面を
隠蔽し、修正タイプする目的の修正手段として使
用するためとくに適する。転写テープのもう1つ
の用途は表面、文書またはサインもしくはそれら
の有色マーキングであり、その際転写リボンは有
色顔料を含む転写被覆層を有する。もう1つの用
途はテキストの点、記号または図面の説明、強調
である。この目的には転写被覆層はとくに透明で
あり、昼光蛍光着色剤で着色される。ここに挙げ
たすべての使用例では乾式で適用され、すなわち
液膜のにじみおよび有害な溶剤の蒸発がないの
で、直ちに再タイプしうることがとくに有利であ
る。このように本発明の転写テープによれば、た
とえば隠蔽被覆層を支持材へ容易に、迅速かつ均
一に適用することができる。本発明の転写テープ
の転写被覆層が透明、すなわちたとえば被覆顔料
を含まない場合、これは着色作用のない単なる隠
蔽のためおよび空気等の作用に敏感な印字の保存
または保護のため使用することができる。 The transfer tape of the present invention is particularly suitable for use as a correction means for the purpose of concealing and correcting erroneously typed letters, markings and drawings in offices, schools and homes. Another use of transfer tapes is the colored marking of surfaces, documents or signs or the like, the transfer ribbon having a transfer coating layer containing colored pigments. Another use is the explanation and emphasis of text points, symbols or drawings. For this purpose, the transfer coating layer is particularly transparent and colored with a daylight fluorescent colorant. In all the applications mentioned here, it is applied dry, ie without smearing of liquid films and evaporation of harmful solvents, so that immediate retyping is particularly advantageous. Thus, according to the transfer tape of the present invention, for example, a concealing coating layer can be applied easily, quickly and uniformly to a support material. If the transfer coating layer of the transfer tape according to the invention is transparent, i.e. does not contain coating pigments, for example, it can be used for mere concealment without any coloring effect and for the preservation or protection of prints that are sensitive to effects such as air. can.
実施例: 次に本発明を例によつて説明する。Example: The invention will now be explained by way of example.
例 1:
着色剤含有転写被覆層を形成するため、まず下
記の分散液を調製する:
溶剤可溶性ポリウレタン(Permuthane
U4924)(イソプロピルアルコール/トルエン
混合比1:1中25%) 19.0重量部
イソプロパノール 10.0重量部
トルエン 35.0重量部
レーキ(Printan G) 1.0重量部
エチルセルロールN7(剥離助剤) 1.0重量部
2酸化チタン(Kronos RN34) 29.0重量部
アルミノケイ酸塩P820(隠蔽力改善剤)
5.0重量部
カーボンブラツク(Printax 140V)(着色剤)
0.01重量部
100.01重量部
上記被覆剤をドクタブレードにより18g/m2の
量でシリコーン塗被紙支持材に適用した。次に溶
剤を約100℃の熱風通過によつて蒸発させた。下
記組成を有する水性分散液をドクタブレードを使
用して着色剤含有隠蔽被覆層の表面に適用した:
アクリレート系圧感接着剤(Freihoffのプラス
チツク分散液VP859/6)(アクリルエステル
系コーポリマー) 66.9重量部
水 33.0重量部
湿潤剤または表面活性剤(Byk W) 0.1重量部
100.0重量部
圧感接着剤をドクタブレードで2g/m2の厚さ
に適用した。次に水分を約100℃の熱風通過によ
つて蒸発させた。Example 1: To form a colorant-containing transfer coating layer, the following dispersion is first prepared: Solvent-soluble polyurethane (Permuthane)
U4924) (25% in isopropyl alcohol/toluene mixing ratio 1:1) 19.0 parts by weight Isopropanol 10.0 parts by weight Toluene 35.0 parts by weight Lake (Printan G) 1.0 parts by weight Ethylcellulose N7 (peeling aid) 1.0 parts by weight Titanium dioxide (Kronos RN34) 29.0 parts by weight Aluminosilicate P820 (hiding power improver)
5.0 parts by weight Carbon Black (Printax 140V) (colorant)
0.01 parts by weight 100.01 parts by weight The above coating was applied to the silicone-coated paper support by means of a doctor blade in an amount of 18 g/m 2 . The solvent was then evaporated by passing hot air at about 100°C. An aqueous dispersion having the following composition was applied to the surface of the colorant-containing hiding coating layer using a doctor blade: Acrylate pressure-sensitive adhesive (Freihoff's plastic dispersion VP859/6) (acrylic ester copolymer) 66.9wt. Part water 33.0 parts by weight Wetting agent or surfactant (Byk W) 0.1 parts by weight 100.0 parts by weight The pressure-sensitive adhesive was applied with a doctor blade to a thickness of 2 g/m 2 . The moisture was then evaporated by passing hot air at about 100°C.
得られた転写テープは、紙にタイプした文字を
隠蔽するためとくに適当であつた。被覆片は迅
速、均一に適用し、その上に直ちに再タイプする
ことができた。適用は、市販のハンドローラを用
いて行つた。 The resulting transfer tape was particularly suitable for concealing typed characters on paper. The coating strip could be applied quickly and evenly and immediately retyped over. Application was carried out using a commercially available hand roller.
例 2:
例1を変更して、着色剤含有転写被覆層を形成
するために、次の配合を使用した:
ポリウレタン(Bayer社のDesmolac2100)
5.0重量部
メチルエチルケトン 30.0重量部
トルエン 28.6重量部
Maxilonbrillantflavin 10GFF(BASF社)
1.0重量部
Basonyl−Rot 540(BASF社) 0.4重量部
2酸化チタン(Kronos社のRN34) 29.0重量部
アルミノケイ酸塩P820(Degussa社) 5.0重量部
エチルセルロースN7(Hercules社) 1.0重量部
得られた転写テープの転写被覆層は良好な隠蔽
力を有し、着色(オレンジ)され、蛍光を示され
なかつた。Example 2: Modifying Example 1, the following formulation was used to form a colorant-containing transfer coating: Polyurethane (Desmolac 2100 from Bayer)
5.0 parts by weight Methyl ethyl ketone 30.0 parts by weight Toluene 28.6 parts by weight Maxilonbrillantflavin 10GFF (BASF)
1.0 parts by weight Basonyl-Rot 540 (BASF) 0.4 parts by weight Titanium dioxide (RN34 from Kronos) 29.0 parts by weight Aluminosilicate P820 (Degussa) 5.0 parts by weight Ethylcellulose N7 (Hercules) 1.0 parts by weight Transfer obtained The transfer coating layer of the tape had good hiding power and was colored (orange) and showed no fluorescence.
例 3:
例1を変更して、着色剤含有転写被覆層を形成
するために、下記配合を使用した:
線状飽和ポリエステル(Good year社の
VitelPE 700) 4.0重量部
メチルエチルケトン 30.0重量部
トルエン 31.0重量部
白色顔料(硫化亜鉛)(Sachtleben GmbH社
のSachtolithL) 25.0重量部
エチルセルロースN7(Hercules社) 1.0重量部
Blaze Orange T15(Dayglo社) 9.0重量部
得れた転写テープの転写被覆層は良好な隠蔽力
を有し、着色(オレンジ)され、蛍光を示した。Example 3: Modifying Example 1, the following formulation was used to form a colorant-containing transfer coating: Linear saturated polyester (from Good Year)
VitelPE 700) 4.0 parts by weight Methyl ethyl ketone 30.0 parts by weight Toluene 31.0 parts by weight White pigment (zinc sulfide) (Sachtolith L from Sachtleben GmbH) 25.0 parts by weight Ethylcellulose N7 (Hercules) 1.0 parts by weight Blaze Orange T15 (Dayglo) 9.0 parts by weight Obtained The transfer coating layer of the transferred transfer tape had good hiding power and was colored (orange) and fluorescent.
例 4:
例1を変更して、着色剤含有転写被覆層を形成
するために下記配合を使用した:
スチレン−イソプレン−スチレンコ−ポリマー
(Shell社のCariplex TR 1107) 4.7重量部
メチルエチルケトン 42.0重量部
トルエン 42.0重量部
Redglo Soluble Toner GF13(Redglo社)
8.0重量部
エチルセルロースN22(Hercules社) 1.0重量部
ステアリン酸アルミニウムAlugel TH34
0.8重量部
ケイ酸(Degussa社のAerosil 200) 1.0重量部
得られた転写テープの転写被覆層は透明で着色
(オレンジ)していた。Example 4: Modifying Example 1, the following formulation was used to form the colorant-containing transfer coating layer: Styrene-isoprene-styrene copolymer (Cariplex TR 1107 from Shell) 4.7 parts by weight Methyl ethyl ketone 42.0 parts by weight Toluene 42.0 parts by weight Redglo Soluble Toner GF13 (Redglo)
8.0 parts by weight Ethyl cellulose N22 (Hercules) 1.0 parts by weight Aluminum stearate Alugel TH34
0.8 parts by weight Silicic acid (Aerosil 200 from Degussa) 1.0 parts by weight The transfer coating layer of the resulting transfer tape was transparent and colored (orange).
例 5:
例1を変更して、着色剤含有転写被覆層を形成
するために、下記配合を使用した:
ビニルプロピオネート系ポリマー分散液
(BASF社のPropionfan 6D) 20.0重量部
2酸化チタン(Kronos社のRNCX) 30.0重量部
アルミノケイ酸塩P820 5.0重量部
水 28.5重量部
水溶性メチルセルロース(Wolff&Co.社の
Walocel MW50GB) 1.0重量部
イソプロパノール 14.0重量部
シリコーンを含まないハロゲン化した有機化合
物の水溶液(Ho¨chst AG社の抑泡剤 SF)
1.0重量部
ナトリウムジオクチルスルホサクシネート
(Lutensit ABO/BASF社の湿潤剤)
0.5重量部
得られた転写テープの転写被覆層は良好な隠蔽
力を有し、白色であつた。Example 5: Modifying Example 1, the following formulation was used to form a colorant-containing transfer coating layer: Vinyl propionate-based polymer dispersion (Propionfan 6D from BASF) 20.0 parts by weight of titanium dioxide ( RNCX from Kronos) 30.0 parts aluminosilicate P820 5.0 parts water 28.5 parts water-soluble methylcellulose (from Wolff & Co.
Walocel MW50GB) 1.0 parts by weight Isopropanol 14.0 parts by weight Silicone-free aqueous solution of halogenated organic compounds (foam suppressor SF from Ho¨chst AG)
1.0 parts by weight Sodium dioctyl sulfosuccinate (Lutensit ABO/BASF wetting agent)
0.5 parts by weight The transfer coating layer of the resulting transfer tape had good hiding power and was white in color.
Claims (1)
感接着被膜との間にプラスチツク結合転写被覆層
が配置され、プラスチツク結合転写被覆層は圧感
接着被膜に対し、支持材に対するよりも強い接着
力を有する可撓性の多層転写テープにおいて、プ
ラスチツク結合転写被覆層が可溶性セルロース誘
導体を含有し、該誘導体は転写被覆層中に0.5〜
5重量%の量で存在することを特徴とする修正お
よびマーキング用の可撓性多層転写テープ。 2 セルロース誘導体がエチルセルロースである
請求項1記載の転写テープ。 3 支持材がプラスチツクまたはシリコーン塗被
紙またはその双方からなる請求項1または2記載
の転写テープ。 4 転写被覆層がプラスチツク結合剤としてポリ
ウレタンを含む請求項1から3までのいずれか1
項記載の転写テープ。 5 ポリウレタンが脂肪族1成分ポリウレタンで
ある請求項4記載の転写テープ。 6 着色剤が転写被覆層中に存在する請求項1か
ら5までのいずれか1項記載の転写テープ。 7 着色剤が顔料である請求項6記載の転写テー
プ。 8 顔料が隠蔽力の高い白色顔料である請求項7
記載の転写テープ。 9 顔料が有機または無機有色顔料である請求項
7記載の転写テープ。 10 テキストの文字または図の表示を強調する
ため、着色剤が蛍光染料である請求項6記載の転
写テープ。 11 塩基性染料を添加する場合、転写被覆層が
この染料のためのレーキを含む請求項1から10
までのいずれか1項記載の転写テープ。 12 圧感接着被膜と転写被覆層の厚さの比が
1:4〜1:12である請求項1から11までのい
ずれか1項記載の転写テープ。 13 手動器具の中に巻取つた形の請求項1記載
の転写テープ。 14 可溶性セルロース誘導体を含むプラスチツ
ク溶液を常用アプリケータによつて可撓性支持材
へ適用し、高めた温度で溶剤を蒸発させ、次に圧
感接着剤を含む水性分散液を形成し、転写被覆層
へ常用のアプリケータによつて適用し、次いで水
を蒸発させることを特徴とする修正およびマーキ
ング用の可撓性多層転写テープの製法。[Scope of Claims] 1 A support material and a pressure-sensitive adhesive coating, wherein a plastic-bonded transfer coating layer is disposed between the support material and the pressure-sensitive adhesive coating, and the plastic-bonded transfer coating layer provides support to the pressure-sensitive adhesive coating. In a flexible multilayer transfer tape that has a stronger adhesion to the material, the plastic-bonded transfer coating layer contains a soluble cellulose derivative, which is present in the transfer coating layer in an amount of 0.5 to
Flexible multilayer transfer tape for correction and marking, characterized in that it is present in an amount of 5% by weight. 2. The transfer tape according to claim 1, wherein the cellulose derivative is ethyl cellulose. 3. A transfer tape according to claim 1 or 2, wherein the support material comprises plastic or silicone coated paper or both. 4. Any one of claims 1 to 3, wherein the transfer coating layer contains polyurethane as a plastic binder.
Transfer tape as described in section. 5. The transfer tape according to claim 4, wherein the polyurethane is an aliphatic one-component polyurethane. 6. Transfer tape according to any one of claims 1 to 5, wherein a colorant is present in the transfer coating layer. 7. The transfer tape according to claim 6, wherein the colorant is a pigment. 8. Claim 7, wherein the pigment is a white pigment with high hiding power.
Transfer tape as described. 9. The transfer tape according to claim 7, wherein the pigment is an organic or inorganic colored pigment. 10. The transfer tape according to claim 6, wherein the coloring agent is a fluorescent dye to emphasize the display of text characters or figures. 11. If a basic dye is added, the transfer coating layer comprises a lake for this dye.
The transfer tape according to any one of the preceding items. 12. The transfer tape according to any one of claims 1 to 11, wherein the ratio of the thicknesses of the pressure sensitive adhesive coating and the transfer coating layer is from 1:4 to 1:12. 13. The transfer tape of claim 1 in the form of a roll in a hand-held instrument. 14 A plastic solution containing a soluble cellulose derivative is applied to a flexible support by a conventional applicator, the solvent is evaporated at elevated temperature, and an aqueous dispersion containing a pressure-sensitive adhesive is then formed to form a transfer coating layer. A process for the preparation of a flexible multilayer transfer tape for correction and marking, characterized in that it is applied by a conventional applicator to a surface and then the water is evaporated.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3741022A DE3741022C3 (en) | 1987-12-03 | 1987-12-03 | Multilayer, flexible transfer belt |
DE3741022.9 | 1987-12-03 | ||
DE3835783A DE3835783C2 (en) | 1987-12-03 | 1988-10-20 | Multilayer flexible transfer belt, method of manufacture and uses thereof |
DE3835783.6 | 1988-10-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0214185A JPH0214185A (en) | 1990-01-18 |
JPH0549476B2 true JPH0549476B2 (en) | 1993-07-26 |
Family
ID=25862407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63304284A Granted JPH0214185A (en) | 1987-12-03 | 1988-12-02 | Flexible multilayer transfer ribbon and manufacture thereof |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0318804B1 (en) |
JP (1) | JPH0214185A (en) |
KR (1) | KR920010112B1 (en) |
AR (1) | AR247849A1 (en) |
AU (1) | AU618768B2 (en) |
BR (1) | BR8806405A (en) |
DE (3) | DE3741022C3 (en) |
DK (1) | DK173619B1 (en) |
ES (1) | ES2051287T3 (en) |
FI (1) | FI97286C (en) |
MX (1) | MX169629B (en) |
NO (1) | NO176832C (en) |
PT (1) | PT89133B (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3741022C3 (en) * | 1987-12-03 | 1994-12-22 | Pelikan Ag | Multilayer, flexible transfer belt |
DE3925130A1 (en) * | 1989-07-28 | 1991-01-31 | Pelikan Ag | MULTILAYER, FLEXIBLE MARKING BAND |
DE69121158T2 (en) * | 1990-10-05 | 1996-12-19 | Fuji Kagaku Shikogyo | Transfer strips for correction |
DE4137936A1 (en) * | 1991-11-18 | 1993-05-19 | Pelikan Ag | TRANSFER TAPE |
WO1996028308A1 (en) * | 1995-03-14 | 1996-09-19 | Pritt Produktionsgesellschaft Mbh | Multi-layer, flexible transfer strip, a process for its production and its use in a hand device |
JP2688184B2 (en) * | 1995-04-07 | 1997-12-08 | フジコピアン株式会社 | Pressure-sensitive correction tape |
US6162492A (en) * | 1996-01-26 | 2000-12-19 | Citius Burotechnik Gmbh | Multi-layer correction and/or marking material, process for its production and its use |
DE19617850C1 (en) | 1996-05-03 | 1997-06-05 | Henkel Kgaa | Multilayered flexible transfer strip with auxiliary support and pressure sensitive adhesive layer |
DE19744957C1 (en) * | 1997-10-10 | 1999-07-29 | Pritt Produktionsgesellschaft | Multi-layer, flexible correction tape |
JP3705325B2 (en) * | 1998-06-10 | 2005-10-12 | 株式会社トンボ鉛筆 | Pressure sensitive transfer correction tape |
BR9916910B1 (en) * | 1999-01-15 | 2009-01-13 | correction tape having dye migration blocking properties. |
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JPS61286194A (en) * | 1985-06-14 | 1986-12-16 | Alps Electric Co Ltd | Thermal transfer medium |
JPS62130888A (en) * | 1985-12-04 | 1987-06-13 | Alps Electric Co Ltd | Thermal transfer medium |
JPS62191192A (en) * | 1985-12-24 | 1987-08-21 | イ−ストマン コダック カンパニ− | Cellulose group bonding agent for pigment dative element used for pigment heat transfer |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1147244B (en) * | 1958-10-01 | 1963-04-18 | Columbia Ribbon Carbon Mfg | Transfer media and process for its manufacture |
US3515572A (en) * | 1958-11-26 | 1970-06-02 | Tipp Ex Fabrikation | Transfer sheet for obliterating typed character |
NL287666A (en) * | 1962-01-20 | |||
GB1135020A (en) * | 1965-05-21 | 1968-11-27 | Dabisch Wolfgang | Typewriter ink ribbon |
GB1171925A (en) * | 1966-06-24 | 1969-11-26 | Carbon Paper Co Ltd | Process for Producing a Copying Paper. |
GB1219567A (en) * | 1966-12-16 | 1971-01-20 | Datacopy Ltd | Improvements in and relating to transfer sheets |
DE6902468U (en) * | 1968-01-24 | 1969-09-25 | Abrogio Cuneo | TYPEWRITER TAPE ALSO FOR CORRECTING TYPOGRAPHICAL ERRORS |
US3942621A (en) * | 1970-04-28 | 1976-03-09 | Mac Karlan | Method of and article for masking |
US3924728A (en) * | 1974-02-04 | 1975-12-09 | Columbia Ribbon Carbon Mfg | Pressure-adhesive correction materials and method for producing same |
DE2626891A1 (en) * | 1976-06-16 | 1977-12-29 | Ernst Dipl Chem Dr Beyer | Correcting sheet for covering errors on paper - contains plastic carrier foil, adhesive separating layer, pigment layer and adhesive layer |
DE3143320C2 (en) * | 1981-10-31 | 1984-10-11 | Pelikan Ag, 3000 Hannover | Foil writing set for overhead projection |
DE3741022C3 (en) * | 1987-12-03 | 1994-12-22 | Pelikan Ag | Multilayer, flexible transfer belt |
-
1987
- 1987-12-03 DE DE3741022A patent/DE3741022C3/en not_active Expired - Lifetime
-
1988
- 1988-10-20 DE DE3835783A patent/DE3835783C2/en not_active Expired - Lifetime
- 1988-11-22 EP EP88119402A patent/EP0318804B1/en not_active Expired - Lifetime
- 1988-11-22 DE DE3889201T patent/DE3889201D1/en not_active Expired - Lifetime
- 1988-11-22 AU AU25808/88A patent/AU618768B2/en not_active Ceased
- 1988-11-22 ES ES88119402T patent/ES2051287T3/en not_active Expired - Lifetime
- 1988-11-30 PT PT89133A patent/PT89133B/en not_active IP Right Cessation
- 1988-11-30 NO NO885336A patent/NO176832C/en unknown
- 1988-11-30 MX MX1400488A patent/MX169629B/en unknown
- 1988-11-30 DK DK198806678A patent/DK173619B1/en not_active IP Right Cessation
- 1988-12-01 BR BR888806405A patent/BR8806405A/en not_active IP Right Cessation
- 1988-12-01 FI FI885585A patent/FI97286C/en active IP Right Grant
- 1988-12-01 AR AR88312601A patent/AR247849A1/en active
- 1988-12-02 JP JP63304284A patent/JPH0214185A/en active Granted
- 1988-12-03 KR KR1019880016154A patent/KR920010112B1/en not_active IP Right Cessation
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56106893A (en) * | 1979-12-28 | 1981-08-25 | Toppan Printing Co Ltd | Transfer sheet |
JPS58101095A (en) * | 1981-12-12 | 1983-06-16 | Fuji Kagakushi Kogyo Co Ltd | Heat transfer recording medium |
JPS60234891A (en) * | 1984-05-07 | 1985-11-21 | Pentel Kk | Correction sheet for thermal transfer material |
JPS6122709A (en) * | 1984-07-09 | 1986-01-31 | 日新電機株式会社 | Switchboard |
JPS6124893A (en) * | 1984-07-16 | 1986-02-03 | 動力炉・核燃料開発事業団 | Heat-insulating material structure |
JPS61286194A (en) * | 1985-06-14 | 1986-12-16 | Alps Electric Co Ltd | Thermal transfer medium |
JPS62130888A (en) * | 1985-12-04 | 1987-06-13 | Alps Electric Co Ltd | Thermal transfer medium |
JPS62191192A (en) * | 1985-12-24 | 1987-08-21 | イ−ストマン コダック カンパニ− | Cellulose group bonding agent for pigment dative element used for pigment heat transfer |
Also Published As
Publication number | Publication date |
---|---|
JPH0214185A (en) | 1990-01-18 |
KR890009649A (en) | 1989-08-03 |
DE3835783A1 (en) | 1990-04-26 |
MX169629B (en) | 1993-07-15 |
AR247849A1 (en) | 1995-04-28 |
DK667888D0 (en) | 1988-11-30 |
DE3741022C2 (en) | 1989-11-23 |
DK173619B1 (en) | 2001-05-07 |
FI885585A (en) | 1989-06-04 |
PT89133B (en) | 1993-05-31 |
PT89133A (en) | 1989-12-29 |
DE3889201D1 (en) | 1994-05-26 |
AU618768B2 (en) | 1992-01-09 |
AU2580888A (en) | 1989-06-15 |
DE3741022C3 (en) | 1994-12-22 |
KR920010112B1 (en) | 1992-11-16 |
NO176832B (en) | 1995-02-27 |
DK667888A (en) | 1989-06-04 |
EP0318804A3 (en) | 1990-11-07 |
DE3741022A1 (en) | 1989-06-15 |
FI97286C (en) | 1996-11-25 |
FI97286B (en) | 1996-08-15 |
NO885336D0 (en) | 1988-11-30 |
NO176832C (en) | 1995-06-14 |
EP0318804A2 (en) | 1989-06-07 |
FI885585A0 (en) | 1988-12-01 |
DE3835783C2 (en) | 1998-02-19 |
EP0318804B1 (en) | 1994-04-20 |
BR8806405A (en) | 1989-08-22 |
ES2051287T3 (en) | 1994-06-16 |
NO885336L (en) | 1989-06-05 |
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