JPH0339837B2 - - Google Patents
Info
- Publication number
- JPH0339837B2 JPH0339837B2 JP56095117A JP9511781A JPH0339837B2 JP H0339837 B2 JPH0339837 B2 JP H0339837B2 JP 56095117 A JP56095117 A JP 56095117A JP 9511781 A JP9511781 A JP 9511781A JP H0339837 B2 JPH0339837 B2 JP H0339837B2
- Authority
- JP
- Japan
- Prior art keywords
- paper
- thermal
- seconds
- smoothness
- support
- 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
- 239000000126 substance Substances 0.000 claims description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000002243 precursor Substances 0.000 claims description 6
- 230000000052 comparative effect Effects 0.000 description 15
- 238000007639 printing Methods 0.000 description 15
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 230000007935 neutral effect Effects 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 238000003809 water extraction Methods 0.000 description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 210000003128 head Anatomy 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 238000010009 beating Methods 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 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 2
- 238000003490 calendering Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- -1 malachite green lactone Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 239000010680 novolac-type phenolic resin Substances 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- 239000013055 pulp slurry Substances 0.000 description 2
- 210000004761 scalp Anatomy 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000007651 thermal printing Methods 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- XBQRPFBBTWXIFI-UHFFFAOYSA-N 2-chloro-4-[2-(3-chloro-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(O)C(Cl)=CC=1C(C)(C)C1=CC=C(O)C(Cl)=C1 XBQRPFBBTWXIFI-UHFFFAOYSA-N 0.000 description 1
- ZDRSNHRWLQQICP-UHFFFAOYSA-N 2-tert-butyl-4-[2-(3-tert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)(C)C)=C1 ZDRSNHRWLQQICP-UHFFFAOYSA-N 0.000 description 1
- PWDAUHQMJRBUHP-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3,3-bis[4-(dimethylamino)phenyl]-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C=CC(=CC=2)N(C)C)C(C(Cl)=C(Cl)C(Cl)=C2Cl)=C2C(=O)O1 PWDAUHQMJRBUHP-UHFFFAOYSA-N 0.000 description 1
- 229940073735 4-hydroxy acetophenone Drugs 0.000 description 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000006103 coloring component Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- ZSYJMXLJNPEAGP-UHFFFAOYSA-N methyl n-cyanocarbamate Chemical compound COC(=O)NC#N ZSYJMXLJNPEAGP-UHFFFAOYSA-N 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- 229950000975 salicylanilide Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000004383 yellowing 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
- B41M5/40—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
- B41M5/41—Base layers supports or substrates
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Description
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ãè¡šãDETAILED DESCRIPTION OF THE INVENTION The present invention relates to a thermal paper in which a paper support is provided with a thermosensitive layer containing a normally colorless or slightly pale dye precursor and a phenolic substance that causes the dye precursor to develop color when heated. The present invention relates to a thermal paper with improved printability, in which a thermal layer is provided on the cast surface of the glossy paper. Furthermore, the present invention relates to a thermal paper with good printability and less background fog, in which the extraction pH of the support is 6 to 9. It has been known for a long time that a dye precursor such as crystal violet lactone reacts with a phenolic substance to produce color, and the application of this reaction to thermal paper is described in, for example, Japanese Patent Publication No. 14039/1983. It has been described and is publicly known. The thermal paper of the present invention usually uses a colorless or slightly pale dye precursor and a phenolic substance.
Each of these is separately dispersed in the form of fine particles in an aqueous medium containing a binder, and the respective dispersions are mixed. A heat-sensitive coating liquid is made by adding white inorganic or organic pigments, binders, etc. as appropriate.
This coating liquid is applied to a support, dried, and then calendered to finish the surface in order to further improve the surface smoothness. Generally, when thermal paper is used in a thermal printing method such as a facsimile machine or a printer, an electric current is instantaneously applied to the thermal head to heat it, and the thermal paper is brought into contact with it to print in color. If the contact between the print head and the print head is insufficient, the color density of the print will be low, or the color will be shaded, making it difficult to read. In practice, in order to improve the adhesion between the paper and the head, the surface of the heat-sensitive layer is usually finished by passing a super calender to a Bec. smoothness level (JIS-P8119) of 200 to 1000 seconds. However, in recent high-speed printers and G-standard high-speed facsimile machines, the printing time is very short, so it has been found that even if the Beck smoothness is sufficiently high, unevenness occurs in the printing performance. The inventors of the present invention have conducted extensive studies regarding the reproducibility of printed dots (the shape of the heating resistor is directly reproduced on thermal paper) with printers and facsimile machines, and have found that the basic smoothness of the surface of the heat-sensitive layer alone is insufficient for printing. It was found that the reproducibility was not sufficient. Since the support used in thermal paper is generally paper, the thickness of each bulp fiber is related to the reproducibility of dots during printing, and in order to eliminate this effect,
It has been proposed to provide a heat-sensitive layer on an undercoated support (Japanese Unexamined Patent Publication No. 83841/1983).
However, although providing such an undercoat layer improves printing quality, it is difficult to implement because it requires two coats, which increases the cost. The present inventors investigated a method to improve dot reproducibility without undercoating, and found that
We have arrived at the present invention. The present invention uses glossy paper as a paper support to improve dot reproducibility to a satisfactory degree. Katatsuya paper is a base paper that is made using a circular wire paper machine and cast-dried using a mirror dryer such as a Yankee dryer, so that one side is extremely glossy and the other side is rough. The paper support for conventional thermal paper generally uses high-quality paper and does not use glossy paper. As a result, the smoothness of the paper support is poor, and thermal paper using this as a paper support has uncolored areas along the fiber flow during high-speed printing, and in severe cases, 2 to 4 dots with poor print reproducibility. occurs. This is mainly due to the pulp fibers of the support, and if a thick heat-sensitive layer is applied to eliminate the influence of the pulp fibers, the coloring components will not develop effectively during high-speed printing. This results in high costs. To describe the characteristics of the thermal paper using the paper support according to the present invention in more detail, since the paper support is made using a circular paper machine, the pulp fibers are also oriented in the thickness direction of the paper, making it difficult to make fourdrinier paper. Dots should not be blurred like when using a support in a machine. Since the paper support is cast-dried using a mirror dryer, the cast surface has some fibers that are keratinized and has a smooth finish. For that reason,
When applying a water-based heat-sensitive coating liquid, the smoothness of the support is less likely to return, and even without supercalender treatment, the coating is smoother than that of a paper support produced using a fourdrinier paper machine. The pressure of the super calender in post-processing can also be reduced, resulting in less pressure build-up on the surface of the thermal paper and good printing performance. The smoothness of the cast surface of the paper support was 80 to 300 seconds in terms of Beck smoothness, and the printing performance was particularly good when it was 100 seconds or more. Because the back surface of the support is not cast-dried, the back surface has large irregularities, and when printing with facsimile, there is a large frictional resistance with the platen roll, and the thermal paper runs smoothly. The Beck smoothness of the back surface is less than 50 seconds. As described in Japanese Patent Application Laid-Open No. 54-115255, the paper is smoothed by passing it between stainless steel rolls,
The smoothness of the surface on which the heat-sensitive layer is provided
When the time is set to 500 seconds or more, the Betzk smoothness of the back surface also becomes quite high, usually 350 seconds or more. When such thermal paper is used for facsimile printing, the frictional resistance against the platen roll is small and the running properties of the thermal paper are very poor. When Katatsuya paper made so that the water extraction pH is around neutral 6 to 9 is used as a paper support, the shelf life of thermal paper (texture after being left at 60â for 24 hours, 40â90 %RH after being left for 24 hours) and printability, making it possible to produce ideal thermal paper. Paper with a water extraction rating of 6 to 9 is a so-called neutral paper, and can be made using a commercially available neutral sizing agent and an internally added filler such as calcium carbonate, talc, or clay. Paper with an extraction pH of less than 6 is generally made by fixing it with vanium sulfate using rosin size, but as a paper support for thermal paper, printing properties are good if the Beck smoothness is 100 seconds or more. , there is a tendency that the long-term shelf life of the scalp becomes poor. Additionally, paper with a pH of over 9 tends to cause yellowing of the paper. The characteristics of the thermal paper of the present invention have been described above, and the materials used will be further described. Typical examples of the colorless to light-colored dye precursor used in the present invention are as follows, but the invention is not limited to these typical examples. Crystal violet lactone, malachite green lactone, 3,3-bis-(paradimethylaminophenyl)-4,5,6,7-tetrachlorophthalide, benzo-β-naphthospiropyran, 3-methyl-di-β -naphthospiropyran,
1,3,3-trimethyl-6'-chloro-8'-methoxyindolylbenzospiropyran, N-phenylrhodamine lactam, 3-ethylamino-6-
Chlorofluorane, 3-morpholino-5,6-benzofluorane, 3-diethylamino-6-methyl-7-chlorofluorane, 3-diethylamino-6,7-dimethylfluorane, 3-diethylamino-7,8- Benzofluorane, 3-diethylamino-6-methoxyfluorane, 3-diethylamino-7-dibenzylaminofluorane, 3-
Diethylamino-7-anilinofluorane, 3-
Diethylamino-5,6-benzo-7-benzylaminofluorane, 3-piperidino-6-methyl-7-anilinofluorane, 3-pyrrolidino-6
-Methyl-7-anilinofluorane, 3-N-ethyl-N-tolylamino-6-methyl-7-anilinofluorane, 3-diethylamino-7-(N
-3-trifluoromethylphenyl)aminofluorane, 3-N-methyl-N-cyclohexylamino-6-methyl-7-anilinofluorane. The phenolic substance used in the present invention has the property of liquefying or vaporizing at room temperature or higher, preferably 70°C or higher and reacting with the color-forming substance to cause it to develop a color, such as 4,4-isopropylidene diphenol, 4,4'-isopropylidene bis(2-chlorophenol), 4,4'-isopropylidene bis(2-tert-butylphenol), 4,4'-
Secondary butylidene diphenol, 4,4'-
Cyclohexylidene diphenol, 4-phenylphenol, 4-hydroxydiphenoxide, methyl-4-hydroxybenzoate, phenyl-
4-hydroxybenzoate, 4-hydroxyacetophenone, salicylic acid anilide, novolac type phenolic resin, halogenated novolac type phenolic resin, α-naphthol, β-naphthol,
2,2-bis(4-hydroxyphenyl)-n-
Mention may be made of phenolic substances such as heptane, but these examples are not intended to limit the scope of the invention. Among them, phenolic substances having two or more hydroxyl groups in one molecule generally exhibit particularly excellent effects. In the present invention, a normally colorless or light-colored color-forming substance and a phenolic substance are dispersed in a binder.
Specifically, it is preferable to grind the particles to a particle size of 5Ό or less. Large particles not only make the coated surface of the thermal paper rough and reduce its commercial value, but also sometimes cause pressure coloring. In addition, activators such as dispersants and antifoaming agents can be used as grinding aids if necessary, and talc can be used as a dewhitening agent or to prevent the coated material from sticking to the thermal head during thermal printing. Fillers such as clay, calcium carbonate, etc. can also be added. Additionally, a surfactant or the like may be added to improve coating properties. In addition, in order to reduce pressure coloring, which occurs when scratched, rubbed, or pressure causes stains on the scalp, waxes can be finely pulverized in the same way as color-forming substances and phenolic substances, or they can be made into an emulsion and placed in a dispersion. It is also possible to add it to. Thermofusible binders cannot be used because they stick to the heat-generating head, and highly water-soluble binders such as starch, polyvinyl alcohol, carboxymethyl cellulose, styrene-maleic acid copolymers, hydroxyethyl cellulose, and casein are generally used. Molecular agents are used. When coating, drying is performed at a relatively low temperature using a coater head such as an air knife, rubber blade, steel blade, roll, or extrusion. Furthermore, if the paper is coated only, the surface smoothness is poor, the adhesion to the heating head is poor, and the thermal conductivity is poor, so it cannot exhibit sufficient performance as a thermal paper. Smoothing treatment can also be carried out by methods such as , gloss calendering, brushing, etc. Next, in order to specifically explain the present invention, examples will be described and explained. Example 1 A wood pulp (LBKP 80% NBKP 20%) slurry beaten to a beating degree of 63°SR was internally added with rosin size at 1.2% based on the pulp and talc at 5% based on the pulp, and then an aqueous solution of vanium sulfate was added to make the pulp. The pH of the slurry was adjusted to 5.6, and paper was made using a circular mesh paper machine.
Weigh by drying with Yankee dryer
A 52 g/m 2 acidic monochrome paper was obtained. The base smoothness of the cast surface of this acidic monochrome paper is 154 seconds, and the water extraction pH is
It was 5.7. The Beck smoothness of the back surface was 13 seconds. Comparative Example 1 and Comparative Example 2 The final pulp slurry prepared in Example 1 was made into paper using a Fourdrinier paper machine, and dried using a multi-tube dryer to a weight of 52
g/m 2 of acidic high-quality paper was obtained. This acidic high-quality paper
The surface smoothness is 52 seconds, and the water extraction pH is 5.7.
It was hot. (Comparative Example 1). This paper was then finished using a super calender to achieve a smoothness of 150 seconds on the front surface. (Comparative Example 2). Example 2 Light calcium carbonate (trade name: Calcium Carbonate PC, manufactured by Shiraishi Kogyo) was added internally to a slurry of wood pulp (LBKP 80%, NBKP 20%) beaten to a degree of beating of 63°SR, and 10% of the pulp was added, and a sizing agent was added. As a fixing agent for the sizing agent, cationic starch (CATO-F, manufactured by National Starch) was added at 0.3% to the pulp and 0.6% to the pulp. The paper was made into a paper using a Yankee dryer and dried using a Yankee dryer to obtain a neutral glossy paper with a basis weight of 52 g/m 2 . The base smoothness of the cast surface of this neutral gloss paper is 130 seconds,
The water extraction pH was 8.2. The Beck smoothness of the back surface was 16 seconds. Comparative Example 3, Comparative Example 4 The final pulp slurry prepared in Example 2 was made into paper using a Fourdrinier paper machine, dried using a multi-tube dryer, and weighed.
A neutral high-quality paper of 52 g/m 2 was obtained. The surface smoothness of this neutral high-quality paper is 54 seconds, and the water extraction pH is 8.2.
It was hot. (Comparative Example 3). Furthermore, the paper of Comparative Example 3 was produced using a supercalender with a Beck smoothness of 150 seconds. (Comparative Example 4). Comparative Example 5 The paper obtained in Comparative Example 3 was passed between stainless steel rolls to check the smoothness of the side on which the heat-sensitive layer was to be provided.
Adjusted to 500 seconds. The Beck smoothness of the back surface of this paper was 380 seconds. Preparation of thermal paper A Liquid calcium carbonate PC 7 parts by weight Sodium polyacrylate 0.05 ã Water 7 ã B Liquid stearamide 1 part by weight 5% hydroxyethyl cellulose 5 ã C Liquid 4,4'-isopropylidene diphenol
1 part by weight 5% hydroxyethyl cellulose 5 D Solution 3-N-methyl-N-cyclohexylamino-
6-Methyl-7-anilinofluorane 1 part by weight 5% hydroxyethyl cellulose 5 Solution A was dispersed using a high-speed stirrer. Next, B, C,
Disperse D solution in a ball mill for 48 hours to obtain A:B:
A heat-sensitive coating liquid was prepared by mixing C:D in a weight ratio of 1:5:5:3. This heat-sensitive coating liquid was applied to the paper supports of Examples 1 and 2 and Comparative Examples 1 to 5 using an air knife coater so that the coating amount after drying was 7 g/ m2 , and the temperature was maintained at not higher than 60°C. Dry. (Examples 1 and 2 were coated on the cast side of glossy paper, and Comparative Examples 1 to 5 were coated on the front side of general high-quality paper.)
Furthermore, it was finished using a super calendar to achieve a Beck smoothness of 400 seconds. These thermal papers were tested using a facsimile tester manufactured by Matsushita Electronic Components at a voltage of 1.6V and a pulse width of 1.0ms.
Printing varies up to 3.3 ms, printing density, dot reproducibility, and shelf life of the background (texture change after storage at 60â for 24 hours...referred to as heat resistant shelf life), and 40â, 90%
Table 1 shows the results of examining the RH, skin change after 24 hours (referred to as humidity and heat storage stability). The thermal paper of Examples 1 and 2 and Comparative Examples 1 to 4 had a large frictional resistance with the platen roll during facsimile printing, and the thermal paper ran smoothly, but the paper of Comparative Example 5 The frictional resistance with the roll was small, and the running properties of the thermal paper were very poor, making it unusable for practical use. ãtableã
Claims (1)
ç©è³ªãäž»ãšããŠçµåããŠãªãæç±å±€ããçŽæ¯æäœ
äžã«èšããæç±çŽã«ãããŠãæç±å±€ãã䞞網æçŽ
æ©ã§æé ãçé¢ã®ã¿ãã€ã¹ã也ç¥ããçã€ãçŽã®
ãã€ã¹ãé¢ã«èšããããŠããŠã該ãã€ã¹ãé¢ã®ã
ãã¯å¹³æ»åºŠã100ã300ç§ã§ããã€ãçã€ãçŽã®ã
ã€ã¹ãé¢ãšå察åŽã®é¢ã®ããã¯å¹³æ»åºŠã50ç§ä»¥äž
ã§ããããšãç¹åŸŽãšããå°åæ§ãåäžããæç±
çŽã ïŒ çŽæ¯æäœã®æ°ŽæœåºPHããïŒãïŒã§ããç¹èš±è«
æ±ã®ç¯å²ç¬¬ïŒé èšèŒã®æç±çŽã[Scope of Claims] 1. A thermal paper in which a heat-sensitive layer mainly consisting of a combination of a colorless or light-colored dye precursor and a phenolic substance is provided on a paper support, wherein the heat-sensitive layer is made on a circular wire paper machine and is made on one side. Only the cast is provided on the cast surface of dry single-sided paper, and the base smoothness of the cast surface is 100 to 300 seconds, and the base smoothness of the opposite side of the single-sided glossy paper is 50 seconds. A thermal paper with improved printability characterized by the following: 2. The thermal paper according to claim 1, wherein the paper support has a water-extracted pH of 6 to 9.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56095117A JPS57208297A (en) | 1981-06-19 | 1981-06-19 | Heat-sensitive paper enhanced in printability |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56095117A JPS57208297A (en) | 1981-06-19 | 1981-06-19 | Heat-sensitive paper enhanced in printability |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57208297A JPS57208297A (en) | 1982-12-21 |
JPH0339837B2 true JPH0339837B2 (en) | 1991-06-17 |
Family
ID=14128892
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56095117A Granted JPS57208297A (en) | 1981-06-19 | 1981-06-19 | Heat-sensitive paper enhanced in printability |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57208297A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5865695A (en) * | 1981-10-16 | 1983-04-19 | Fuji Photo Film Co Ltd | Heat sensitive recording paper |
JPS5869090A (en) * | 1981-10-22 | 1983-04-25 | Fuji Photo Film Co Ltd | Heat sensitive recording paper |
JPS5869091A (en) * | 1981-10-22 | 1983-04-25 | Fuji Photo Film Co Ltd | Heat sensitive recording paper |
JPS5933180A (en) * | 1982-08-18 | 1984-02-22 | Oji Paper Co Ltd | Production of heat-sensitive recording paper |
JPH0679865B2 (en) * | 1984-08-31 | 1994-10-12 | å¯å£«åçãã€ã«ã æ ªåŒäŒç€Ÿ | Thermal recording material |
JPS61225396A (en) * | 1985-03-29 | 1986-10-07 | æ°çå補çŽæ ªåŒäŒç€Ÿ | Receiving paper for ink jet and thermal transfer |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54115255A (en) * | 1978-02-28 | 1979-09-07 | Canon Inc | Thermographic body |
-
1981
- 1981-06-19 JP JP56095117A patent/JPS57208297A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54115255A (en) * | 1978-02-28 | 1979-09-07 | Canon Inc | Thermographic body |
Also Published As
Publication number | Publication date |
---|---|
JPS57208297A (en) | 1982-12-21 |
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