WO2016016084A1 - Wärmeempfindliches aufzeichnungsmaterial mit salicylsäure-derivat als mit einem farbstoffvorläufer reaktionsfähiger (farb-)entwickler - Google Patents
Wärmeempfindliches aufzeichnungsmaterial mit salicylsäure-derivat als mit einem farbstoffvorläufer reaktionsfähiger (farb-)entwickler Download PDFInfo
- Publication number
- WO2016016084A1 WO2016016084A1 PCT/EP2015/066874 EP2015066874W WO2016016084A1 WO 2016016084 A1 WO2016016084 A1 WO 2016016084A1 EP 2015066874 W EP2015066874 W EP 2015066874W WO 2016016084 A1 WO2016016084 A1 WO 2016016084A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- heat
- sensitive recording
- recording layer
- salicylic acid
- recording material
- Prior art date
Links
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
-
- 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
- B41M5/323—Organic colour formers, e.g. leuco dyes
- B41M5/327—Organic colour formers, e.g. leuco dyes with a lactone or lactam ring
- B41M5/3275—Fluoran compounds
-
- 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
- B41M5/337—Additives; Binders
- B41M5/3372—Macromolecular compounds
-
- 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
- B41M5/337—Additives; Binders
- B41M5/3377—Inorganic compounds, e.g. metal salts of organic acids
Definitions
- the invention first relates to a heat-sensitive recording material having a web-shaped substrate and at least one heat-sensitive recording layer formed on at least one of the two sides of the web-shaped substrate, said heat-sensitive recording layer at least one dye precursor and at least one salicylic acid derivative than with this at least one dye precursor contains reactive (color) developer.
- reactive (color) developer to be reactive with a dye precursor, in the context of the present invention in all its embodiments proposed here, means that this at least one salicylic acid derivative reacts with this at least one dye precursor with sufficient supply of external heat to form a visually recognizable printed image.
- Heat-sensitive and color-responsive to the supply of external heat recording materials have been known for many years and enjoy a basically unbroken popularity, which is due, inter alia, that their use for the ticket and / or proof of purchase issuing businessman with great advantages connected is. Because the color-forming components, that is, dye precursors and color-responsive developers (also called color acceptors) in such heat-sensitive recording processes are contained in the recording material itself, the toner and color-cartridge-free thermal printers, which are therefore thermally sensitive in their function no longer need to be controlled by anyone regularly, be set up in large numbers. Thus, this innovative technology has largely prevailed, especially in public transport and retail.
- Bisphenol A that is 2,2 bis (4-hydroxyphenyl) propane, and Bisphenol-S, which is 4,4'-dihydroxydiphenylsulfone,
- thermosensitive recording material comprising
- thermosensitive recording layer is the heat-sensitive recording layer further
- the (color) developer that is the 3,5-di ( ⁇ -methylbenzyl) salicylic acid, auxiliary component according to the invention introduced above, whereby the function of this auxiliary component supporting the (color) developer can be described as a proton transfer inhibitor ,
- 3,5-di ( ⁇ -methylbenzyl) salicylic acid also to be named as 2-hydroxy-3,5-bis (1-phenylethyl) benzoic acid, can be represented as a component according to the following FIG. 1.
- FIG. 1 is a diagrammatic representation of FIG. 1:
- 3,5-di ( ⁇ -methylbenzyl) salicylic acid is a derivative of salicylic acid.
- Another known salicylic acid derivative is acetylsalicylic acid, which is known under the trade name Aspirin® as a very common analgesic. So go both Aspirin ® as well as this side proposed as (color) developer for heat-sensitive recording layer 3,5-di ( ⁇ -methylbenzyl) salicylic acid respectively from the same starting molecule.
- Salicylic acid as such can be obtained from accessory constituents of wood by oxidative separation of the glucoside saline. Specific high concentrations are included, for example, in the bark of willows. It is hardly necessary to emphasize that 3,5-di (a-methylbenzyl) salicylic acid is largely or completely biodegradable.
- polyvinylpyrrolidone can be described as preventing or at least hindering the above-mentioned proton transfer from the (color) developer to the dye precursor and therefore preventing the "climate" buildup, that is, the undesirable whitening of the recording layer .
- Polyvinylpyrrolidone whose preferred molecular weight in the context of the present invention is ideally in a range from 9,100 to 10,500 g / mol, can be represented according to the following FIG. 2.
- FIG. 2 is a diagrammatic representation of FIG. 1
- the heat-sensitive recording material proposed on this side thus has a heat-sensitive recording layer which in a surprising, but completely convincing manner for the recording material a.) Has high sensitivity to desired print image-initiating heat, for example caused by the energy pulses of a thermal printing head . b. ) a sufficient and convincing white for the market without unduly annoying background graying and
- the 3,5-di ( ⁇ -methylbenzyl) salicylic acid used as the (color) developer is a most or fully biodegradable component that, through a common starter molecule, is related to products used in both humanitarian and veterinary medical and therapeutic applications to make obsolete all sorts of concerns about health concerns and biodegradability.
- Polyvinylpyrrolidone is well known as a component for use in the cosmetics industry, here inter alia in hair spray, and in the food industry, so that this component is beyond any doubt in terms of their health and environmental safety.
- thermosensitive recording material proposed here preferably comprises as a possible dye precursor in the thermosensitive recording layer at least one substance selected from the list comprising: 3-diethylamino-6-methyl-7-anilinofluoran, 3-dibutylamino-6-methyl 7-anilinofluoran, 3- (N-methyl-N-propyl) amino-6-methyl-7-anilinofluoran, 3- (N-ethyl-N-isoamyl) amino-6-methyl-7-anilinofluoran, 3- ( N-methyl-N-cyclohexyl) amino-6-methyl-7-anilinofluoran, 3- (N-ethyl-N-tolyl) amino-6-methyl-7-anilinofluoran and 3- (N-ethyl-N-tetrahydrofuryl) amino-6-methyl-7-anilinofluoran.
- 3-dibutylamino-6-methyl-7-anilinofluoran also known as O
- the heat-sensitive recording layer on an amount of dye precursor preferably based on fluoran, in particular 3-dibutylamino-6-methyl-7-anilinofluoran, which ideally in a range of 0.20 g / m 2 to 0.70 g / m 2 , more preferably in a range of 0.30 g / m 2 to 0.50 g / m 2 .
- fluoran in particular 3-dibutylamino-6-methyl-7-anilinofluoran
- thermosensitive recording material with a sufficient whiteness of the heat-sensitive recording layer to ensure a wt .-% (atro) related ratio of
- the present invention also provides that the heat-sensitive recording material according to the invention can completely dispense with sensitizers, which in the context of the present invention as preferred and consistent is seen.
- sensitizers which can be included to increase the thermal sensitivity, be used in such a case, in particular sensitisers such as: 2- (2H-benzotriazol-2-yl) -p-cresol, benzyl-p-benzyloxy benzoate, methylolstearamide, stearic acid amide, p-benzylbiphenyl, 1, 2-di (phenoxy) ethane, 1, 2-di (m-methylphenoxy) ethane, m-terphenyl, dibenzyl oxalate, benzyl naphthyl ether, dimethyl terephthalate and diphenylsulfone.
- sensitisers such as: 2- (2H-benzotriazol-2-yl) -p-cresol, benzyl-p-benzyloxy benzoate, methylolstearamide, stearic acid amide, p-benzylbiphenyl, 1, 2-di (phenoxy)
- Suitable binders for incorporation into the heat-sensitive recording layer are, for example, water-soluble binders such as starch, hydroxyethylcellulose, methylcellulose, carboxymethylcellulose, gelatin, casein, polyvinyl alcohols, modified polyvinyl alcohols, ethylene-vinyl alcohol copolymers, sodium polyacrylates, acrylamide acrylate Copolymers, acrylamide-acrylate-methacrylate terpolymers and alkali metal salts of styrene-maleic anhydride copolymer or ethylene-maleic anhydride copolymer, which binders can be used alone or in combination with one another; Water-insoluble latex binders such as styrene-butadiene copolymers, acrylonitrile-butadiene copolymers and methyl acrylate-butadiene copolymers are also suitable as binders for incorporation into the heat-sensitive recording layer.
- water-soluble binders such as starch,
- the heat-sensitive recording layer may further contain lubricants and release agents such as waxes, in particular paraffin, oxidized paraffin, polyethylene, polyethylene oxide, stearamides and castor wax.
- lubricants and release agents such as waxes, in particular paraffin, oxidized paraffin, polyethylene, polyethylene oxide, stearamides and castor wax.
- stearates such as Zinc stearate or calcium stearate, because the zinc or calcium contained therein destabilizes the 3,5-di ( ⁇ -methylbenzyl) salicylic acid, whereby their color-forming reaction with the dye precursors occurs in no time without the energy pulse of a thermal print head.
- pigments preferably inorganic pigments and most preferably one or more pigments selected from the list comprising kaolin and aluminum (hydr) oxide, in which kaolin is considered particularly suitable here.
- kaolin is considered particularly suitable here.
- Less suitable in the context of the present invention is primarily calcium carbonate, which due to its pH-orientation in the alkaline range can cause a purple-like base color in the heat-sensitive recording layer.
- a dispersant for the preparation of a pigment dispersion for subsequent incorporation into the heat-sensitive recording layer for example, offer carboxylated polyacrylates, but this is particularly preferred sulfonated polyvinyl alcohol, its combination with the polyvinyl alcohol as the preferred binder for incorporation into the heat-sensitive recording layer than in a very special measure is considered preferred.
- a range of from 12 to 30% by weight (atro) based on the total weight of the heat-sensitive recording layer is particularly suitable, which is narrowed down by the increasing danger of possible thermal printing head Deposits and upwards by an increasing reduction of the sensitivity to the print image causing heat of the thermal printheads.
- Roll coating coater, knife coater, curtain coater or air brush are particularly suitable as coating apparatus for applying the heat-sensitive recording layer.
- the recording layer is preferably between 2 and 6 g / m 2 and even better between 2.2 and 4.8 g / m 2 .
- the heat-sensitive recording material according to the invention comprises a pigment-containing intermediate layer, which is arranged between the substrate and heat-sensitive recording layer.
- Suitable pigments of the intermediate layer are both organic cavity pigments and inorganic pigments, the latter preferably selected from the group comprising natural and calcined kaolin, silica and here especially bentonite and aluminum (hydr) oxide and boehmite here in particular.
- organic cavity pigments and inorganic pigments the latter preferably selected from the group comprising natural and calcined kaolin, silica and here especially bentonite and aluminum (hydr) oxide and boehmite here in particular.
- such an intermediate layer can make a positive contribution to the leveling of the surface to be coated, which reduces the amount of coating color necessarily to be applied for the heat-sensitive recording layer. For this reason, offer to coat the pigment-containing intermediate layer leveling coating, such as Walzenstreichwerke, doctor blade and (roll) doctor blade coating.
- the pigments of this intermediate layer can absorb the heat-liquefied wax constituents of the thermosensitive recording layer in the typeface formation and thus promote a safe and rapid operation of the heat-induced recording.
- the basis weight of the pigment-containing intermediate layer is preferably between 5 and 20 g / m 2, and more preferably between 7 and 11 g / m 2 .
- the heat-sensitive recording material proposed here does not require the heat-sensitive recording layer covering protective layer. If it is nevertheless applied to improve the recording material proposed here against environmental influences such as moisture and UV irradiation, such a protective layer is particularly suitable, which in addition to a diacetone-modified polyvinyl alcohol in a first possible embodiment, further binders, in particular mixtures of different Car- boxyl phenomenon- or Has silanol-modified polyvinyl alcohols. These then make up a maximum of 40 wt .-%, preferably at most 15 wt .-%, - based on the total amount of binder in the protective layer - from.
- the protective layer as a binder exclusively diacetone-modified polyvinyl alcohol.
- the binder content in the protective layer is in a range of from 35 to 65% by weight based on the total weight of the protective layer ,
- Suitable crosslinking aids in the protective layer are, in particular, those selected from the group comprising: boric acid, polyamine, epoxy resin, dialdehyde, formaldehyde oligomers, epiochlorohydrin resin, adipic acid dihydrazide, dimethylurea, melamine-formaldehyde. It is also possible to use mixtures of different crosslinking aids.
- the ratio of the weight% of the binder, in particular of the diacetone-modified polyvinyl alcohol, to the crosslinking aid is in the range from 20: 1 to 5: 1 and more preferably in one Range from 12: 1 to 7: 1.
- the protective layer additionally contains an inorganic pigment.
- the inorganic pigment is selected from the group comprising silicon dioxide, aluminum hydroxide, bentonite, kaolin or a mixture of said inorganic pigments.
- roller coater, knife coater, curtain coater or air brush are particularly suitable as coating devices for applying the protective layer covering the heat-sensitive recording layer.
- the basis weight of the protective layer is preferably between 1, 0 and 3.0 g / m 2 and more preferably between 1, 4 and 2.3 g / m 2 .
- paper Although not limited to paper as a substrate in the context of the present invention, paper and is particularly preferred here ⁇ a non-surface treated base paper, that is a base paper not treated in a size press or a coating device, and
- a base paper with a low pH is recommended.
- the use of calcium carbonate as a pigment within the base paper is possible but not preferred because of possible influence on the heat-sensitive recording layer in the form of graying it.
- kaolin, aluminum (hydr) oxide and especially boehmite and bentonite are particularly well suited as pigments within the base paper.
- films of, for example, polypropylene, polyolefin, and polyolefin-coated papers as substrate are possible to the same extent, although not preferred with regard to the environmental effects of such plastic or plastic-coated papers, without such an embodiment being exclusive having.
- a paper pulp of eucalyptus pulp and other pulp fibers with fillers and water is recognized. Further constituents of the pulp to be added are resin glue for Masseleimung with an amount of 0.6 wt .-% (atro), based on the total weight of the pulp, and other conventional additives, such as kaolin as a pigment and optical brightener. After completion of the pulp this is then fed to a fourdrinier paper machine, where it is processed into a paper web with a basis weight of 35 g / m 2 .
- the paper web is fed into a integrated into the paper machine roller blade coater, where on the front side a pigmented intermediate layer with a basis weight of 9 g / m 2 is applied.
- the coating composition used for the formation of the intermediate layer is
- the paper web is still dried within the paper machine by means of radiant heaters and in contact with hot rolls, smoothed here in a Mehrwalzenglätttechnik and then rolled up as Halbfertigpapiertambour.
- the semi-finished paper drum produced in this way is fed to a coating machine, where the continuously unrolled paper web is fed to a doctor blade coater, where the application of prepared coating compositions in each case to form heat-sensitive recording layers each with a basis weight of 4.2 g / m 2 on the previously applied and already dried pigmented intermediate layer happens.
- a coating machine where the continuously unrolled paper web is fed to a doctor blade coater, where the application of prepared coating compositions in each case to form heat-sensitive recording layers each with a basis weight of 4.2 g / m 2 on the previously applied and already dried pigmented intermediate layer happens.
- the coating composition used for forming the heat-sensitive recording layer there are used:
- the heat-sensitive recording layer is then dried by means of hot-air floating dryer and in contact with hot rolls and smoothed in a Mehrwalzenglätttechnik. Finally, the reeling of the now completed heat-sensitive recording materials according to the invention and the comparative heat-sensitive recording material takes place.
- thermosensitive recording material As claimed, the examples fully confirm the expectations of the world and fully demonstrate the advantages of a thermosensitive recording material as claimed.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Inorganic Chemistry (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201580041620.2A CN106573486B (zh) | 2014-07-29 | 2015-07-23 | 具有水杨酸衍生物作为能与染料前体反应的色彩显色剂的热敏性记录材料 |
US15/329,903 US10131169B2 (en) | 2014-07-29 | 2015-07-23 | Heat-sensitive recording material with salicylic acid derivative as (color) developer reactive with a dye precursor |
KR1020177005461A KR20170038028A (ko) | 2014-07-29 | 2015-07-23 | 염료 전구체와 반응할 수 있는 현색제로서 살리실산 유도체를 이용한 감열 기록 재료 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP14178948.7 | 2014-07-29 | ||
EP14178948.7A EP2979888B1 (de) | 2014-07-29 | 2014-07-29 | Wärmeempfindliches Aufzeichnungsmaterial mit Salicylsäure-Derivat als mit einem Farbstoffvorläufer reaktionsfähiger (Farb-)Entwickler |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2016016084A1 true WO2016016084A1 (de) | 2016-02-04 |
Family
ID=51225428
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2015/066874 WO2016016084A1 (de) | 2014-07-29 | 2015-07-23 | Wärmeempfindliches aufzeichnungsmaterial mit salicylsäure-derivat als mit einem farbstoffvorläufer reaktionsfähiger (farb-)entwickler |
Country Status (6)
Country | Link |
---|---|
US (1) | US10131169B2 (de) |
EP (1) | EP2979888B1 (de) |
KR (1) | KR20170038028A (de) |
CN (1) | CN106573486B (de) |
ES (1) | ES2623811T3 (de) |
WO (1) | WO2016016084A1 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6649620B2 (ja) * | 2016-04-20 | 2020-02-19 | 王子ホールディングス株式会社 | 感熱記録体 |
JP6717055B2 (ja) * | 2016-05-27 | 2020-07-01 | 王子ホールディングス株式会社 | 感熱記録体 |
CN110759800A (zh) * | 2018-07-27 | 2020-02-07 | 南京理工大学 | 一种高能高力学性能电控固体推进剂 |
CN116729012B (zh) * | 2023-06-12 | 2024-09-06 | 河南东方印新材料科技有限公司 | 一种机打纹身转印膜及其生产工艺和使用方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62259887A (ja) * | 1986-05-07 | 1987-11-12 | Fuji Photo Film Co Ltd | 感熱記録材料 |
US5326739A (en) * | 1990-08-06 | 1994-07-05 | Mitsui Toatsu Chemicals, Incorporated | Process for producing 3,5-di(α-methylbenzyl)salicylic acid derivative, and use of polyvalent-metal-modified product thereof as color developer |
US5382560A (en) * | 1991-12-18 | 1995-01-17 | Sanyo Chemical Industries, Ltd. | Color developers and sheets thereof |
US20100048395A1 (en) * | 2008-08-20 | 2010-02-25 | Fujifilm Corporation | Thermosensitive recording material |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10054219C2 (de) * | 2000-11-01 | 2003-04-24 | Mitsubishi Hitec Paper Flensbu | Aufzeichnungsmaterial für das Tintenstrahl-Druckverfahren |
US7021214B2 (en) * | 2003-01-27 | 2006-04-04 | Ricoh Company, Ltd. | Method for issuing label with thermosensitive adhesive |
US20040258857A1 (en) | 2003-06-16 | 2004-12-23 | Eastman Kodak Company | Imaging media with high elastic modulus and improved long term stability |
JP3945705B2 (ja) * | 2003-06-25 | 2007-07-18 | 三光株式会社 | 増感剤分散体の製造方法及び感熱記録体 |
JP2006103312A (ja) * | 2004-09-08 | 2006-04-20 | Ricoh Co Ltd | 透過型感熱記録材料およびその製造方法 |
US7906458B2 (en) * | 2006-09-15 | 2011-03-15 | Ricoh Company, Ltd. | Heat-sensitive recording material and production method thereof |
CN101676119B (zh) * | 2008-09-18 | 2012-10-10 | 张镇华 | 改性水杨酸型树脂显色剂 |
EP2546066B2 (de) | 2011-07-14 | 2018-06-27 | Mitsubishi HiTec Paper Europe GmbH | Druckempfindliches Aufzeichnungsmaterial und Verfahren zur Herstellung |
PL2574645T3 (pl) | 2011-09-30 | 2015-03-31 | Mitsubishi Hitec Paper Europe Gmbh | Akceptor barwy reagujący z prekursorem barwnika w sposób tworzący barwę i wrażliwy na ciepło materiał zapisujący z takim akceptorem barwy |
-
2014
- 2014-07-29 ES ES14178948.7T patent/ES2623811T3/es active Active
- 2014-07-29 EP EP14178948.7A patent/EP2979888B1/de not_active Not-in-force
-
2015
- 2015-07-23 CN CN201580041620.2A patent/CN106573486B/zh not_active Expired - Fee Related
- 2015-07-23 US US15/329,903 patent/US10131169B2/en active Active
- 2015-07-23 KR KR1020177005461A patent/KR20170038028A/ko unknown
- 2015-07-23 WO PCT/EP2015/066874 patent/WO2016016084A1/de active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62259887A (ja) * | 1986-05-07 | 1987-11-12 | Fuji Photo Film Co Ltd | 感熱記録材料 |
US5326739A (en) * | 1990-08-06 | 1994-07-05 | Mitsui Toatsu Chemicals, Incorporated | Process for producing 3,5-di(α-methylbenzyl)salicylic acid derivative, and use of polyvalent-metal-modified product thereof as color developer |
US5382560A (en) * | 1991-12-18 | 1995-01-17 | Sanyo Chemical Industries, Ltd. | Color developers and sheets thereof |
US20100048395A1 (en) * | 2008-08-20 | 2010-02-25 | Fujifilm Corporation | Thermosensitive recording material |
Also Published As
Publication number | Publication date |
---|---|
CN106573486B (zh) | 2019-04-19 |
US10131169B2 (en) | 2018-11-20 |
EP2979888A1 (de) | 2016-02-03 |
KR20170038028A (ko) | 2017-04-05 |
US20170267007A1 (en) | 2017-09-21 |
ES2623811T3 (es) | 2017-07-12 |
EP2979888B1 (de) | 2017-02-22 |
CN106573486A (zh) | 2017-04-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3109059B1 (de) | Wärmeempfindliches aufzeichnungsmaterial | |
EP2033799B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP2979888B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial mit Salicylsäure-Derivat als mit einem Farbstoffvorläufer reaktionsfähiger (Farb-)Entwickler | |
EP3305538A1 (de) | Wärmeempfindliches aufzeichnungsmaterial | |
EP2910384B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial mit einer neuartigen Farbakzeptor-Kombination | |
EP2329959B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial mit Barrierebeschichtung | |
EP2574645B1 (de) | Mit einem Farbstoffvorläufer farbbildend reagierender Farbakzeptor und wärmeempfindliches Aufzeichnungsmaterial mit einem solchen Farbakzeptor | |
EP2279877B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP2033801A1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP2329955B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial mit Authentizitätsmerkmal | |
EP2765007B1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
WO2009033590A1 (de) | Wärmeempfindliches aufzeichnungsmaterial mit rückseitenbeschichtung | |
EP2070714B1 (de) | Verfahren zur Herstellung eines wärmeempfindlichen Aufzeichnungsmaterials | |
DE102016219569A1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP1925459B1 (de) | Verfahren zur Herstellung eines wärmeempfindlichen Aufzeichnungsmaterials mit Authentifikationsmerkmal | |
EP2758249B1 (de) | Aufzeichnungsmaterial zur offset-bedruckung | |
DE102006050420B3 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP2480415B1 (de) | Wärmeempfindliches aufzeichnungsmaterial mit rückseitenbeschichtung | |
EP2505374A1 (de) | Wärmeempfindliches Aufzeichnungsmaterial, seine Verwendung und Verfahren zu seiner Herstellung | |
DE102016219567A1 (de) | Wärmeempfindliches Aufzeichnungsmaterial | |
EP2517889A1 (de) | Wärmeempfindliches Aufzeichnungsmaterial mit Authentifikationsmerkmal | |
EP2414173A1 (de) | Wärmeempfindliches aufzeichnungsmaterial |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 15742222 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 15329903 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 20177005461 Country of ref document: KR Kind code of ref document: A |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 15742222 Country of ref document: EP Kind code of ref document: A1 |