EP0419659A1 - Farbentwickler für druckempfindliches speichermedium, wässrige dispersion eines farbentwicklers und verfahren zur herstellung - Google Patents
Farbentwickler für druckempfindliches speichermedium, wässrige dispersion eines farbentwicklers und verfahren zur herstellung Download PDFInfo
- Publication number
- EP0419659A1 EP0419659A1 EP89907826A EP89907826A EP0419659A1 EP 0419659 A1 EP0419659 A1 EP 0419659A1 EP 89907826 A EP89907826 A EP 89907826A EP 89907826 A EP89907826 A EP 89907826A EP 0419659 A1 EP0419659 A1 EP 0419659A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- color developer
- parts
- color
- rosin
- aqueous dispersion
- 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.)
- Withdrawn
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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
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/132—Chemical colour-forming components; Additives or binders therefor
- B41M5/155—Colour-developing components, e.g. acidic compounds; Additives or binders therefor; Layers containing such colour-developing components, additives or binders
Definitions
- the present invention relates to a color developer for pressure-sensitive recording medium, an aqueous dispersion of a color developer and a process for preparing the same.
- Pressure-sensitive recording mediums represented by a pressure-sensitive copying paper which is generally known as a no carbon copying paper develop color when the pressure-sensitive recording mediums are mechanically pressured by means of hand-writing, a typewriter and the like, and are the mediums which can provide plural copied papers at a time. Accordingly, in accordance with the recent high growth of information in the industrial environment, the used amount has been rapidly increased.
- the coloring principle of the pressure-sensitive recording mediums is based upon the generation of a color reaction caused by the contact of a color developer with a pressure-sensitive colorless dye solution flowed from a microcapsule destroyed by printing pressure of a typewriter and the like between the coated surface of an upper paper coated with a microcapsule of a non-volatile type solvent containing an electron donative organic compound (so-called pressure-sensitive colorless dye) and the coated surface of a lower paper coated with an aqueous coating composition containing an electron acceptive color developer.
- inorganic solid acid such as activated clay or attapulgite, various phenolic resins, aliphatic or aromatic carboxylic acids and metallic salts thereof have been conventionally used (Japanese Unexamined Patent Publication No. 32011/1973).
- the inorganic solid acid has defects that the inorganic solid acid type color developer is influenced by light, gas, moisture and the like and the printed mark generated from the developer easily disappears or fades, and the viscosity index is wrong when the inorganic solid acid is used in a paint.
- the phenolic resin has defects that color fastness to light at printing is low and the color developer layer is yellowed by light and gas.
- aromatic carboxylic acid polyvalent metallic salts have been used because the metallic salts is excellent in color fastness to light at printing and shows little yellowing of a color developer layer caused by light or gas.
- polyvalent metallic salts of salicylic acids have been widely used.
- the polyvalent metallic salts of salicylic acids have the above-mentioned various excellent properties, the polyvalent metallic salts have a serious defect of poor waterproofness at printing.
- salicylic acids wherein various oil soluble groups are introduced into the aromatic ring remove the above-mentioned defects to a certain degree.
- the salicylic acids are sufficiently practical matters, and in particular there is a room for improving initial color-forming properties and waterproofness.
- a method for coating a substrate for a recording medium with a color developer As a method for coating a substrate for a recording medium with a color developer, a method for coating a support such as paper with an aqueous dispersion of a color developer is well known.
- a method for preparing the above-mentioned aqueous dispersion for instance, a method for using a water soluble polymer such as polyvinyl alcohol, sodium polyacrylate or sodium polystyrenesulfonate as a dispersing agent, and wet grinding the dispersing agent, water and a color developer by means of Kady mill, sand mill, ball mill or the like, has been generally employed.
- the particle size of the color developer in the obtained aqueous dispersion is usually at least 1 ⁇ m. Therefore, the storage stability of the dispersion deteriorate and the surface area of the color developer comes to be small. Accordingly, there is a defect that desired color developing properties are not exhibited.
- the present invention aims at providing an excellent color developer and an excellent aqueous dispersion thereof improved in initial color-forming properties and waterproofness which are the defects of the above-mentioned polyvalent metallic salts of salicylic acids while maintaining color-forming properties, NO x gas yellowing resistance and the like, and remarkably improved in storage stability which is a defect of a method for preparing an aqueous dispersion thereof.
- the present inventors have been eagerly studied concerning a compound which can be used together with polyvalent metallic salts of salicylic acids.
- a specific polyvalent metallic salt of a rosin-modified phenolic resin is used, it has been for the first time found that the initial color-forming properties and waterproofness which are the defects of a salicylic acid color developer are remarkably improved while maintaining the merits of the salicylic acid color developer.
- the present invention has been accomplished based upon the novel finding.
- the present invention relates to (1) a color developer for pressure-sensitive recording medium characterized in that a polyvalent metallic salt of a salicylic acid and a polyvalent metallic salt of a rosin-modified phenolic resin are contained, (2) an aqueous dispersion of a color developer containing the color developer, and (3) a method for preparing an aqueous dispersion of a color developer characterized in that an amorphous oligomer and polyvinyl alcohol are used as a dispersing agent when a color developer is mechanically emulsified and dispersed in the presence of a dispersing agent and a solvent.
- salicylic acids mean salicylic acid and various known salicylic acid derivatives, and various salicylic acid derivatives can be effectively used.
- salicylic acid derivatives having an alkyl group of at least 8 carbon atoms, desirably 12 to 20 carbon atoms can be particularly preferably used.
- salicylic acid derivatives are, for instance, 3-methyl salicylic acid, 5-methyl salicylic acid, 3-ethyl salicylic acid, 5-ethyl salicylic acid, 3-t-butyl salicylic acid, 5-t-butyl salicylic acid, 3-phenyl salicylic acid, 5-phenyl salicylic acid, 3,5-di-t-butyl salicylic acid, 3-methyl-5-phenyl salicylic acid, 3-t-butyl-5-(p-t-butylbenzyl) salicylic acid, 3-cyclohexyl-5-( ⁇ , ⁇ -dimethylbenzyl) salicylic acid, 3-phenyl-5-( ⁇ , ⁇ -methylbenzyl) salicylic acid, 3-phenyl-5-( ⁇ , ⁇ -dimethylbenzyl) salicylic acid, 3,5-di( ⁇ -dimethylbenzyl) salicylic acid, 3,5-di( ⁇ , ⁇ -dimethylbenzyl) salicylic acid, and the like.
- salicylic acid-formaldehyde condensate Known various condensates of salicylic acids such as salicylic acid-formaldehyde condensate are also included in the above-mentioned salicylic acids.
- the plasticizer resistance of an image is particularly remarkably improved.
- rosin-modified phenolic resin is defined to as follows.
- the phenols various known phenols, for instance, carbolic acid, cresol, p-t-butylphenol
- rosins which are starting materials of a rosin-modified phenolic resin
- natural rosins such as gum rosin, wood rosin and tall oil rosin
- modified rosins such as disproportionated rosins, hydrogenated rosin, polymerized rosin, rosin modified with maleic acid, rosin modified with fumalic acid and formaldehyde-modified resin
- hydrogenated rosin and disproportionated rosin it is preferable to use hydrogenated rosin and disproportionated rosin.
- Both of salicylic acids and rosin-modified phenolic resin can be easily obtained as polyvalent metallic salts thereof by reacting with a polvalent metallic compound described later with heating in the presence of a catalyst and a solvent described later.
- a polyvalent metallic compound described later for instance, compounds of polyvalent metallic compounds such as magnesium, aluminium, calcium or zinc can be used without any limitation.
- oxides, hydroxides, oxides, hydroxides, chlorides, carbonates and sulfates of the polyvalent metal, and the like can be exemplified.
- zinc oxide, zinc hydroxide, zinc chloride, zinc sulfate, magnesium oxide, aluminium oxide, calcium oxide, titan oxide, manganese oxide, magneisum hydroxide, aluminium hydroxide, calcium hydroxide, and the like can be exemplified.
- zinc oxide it is preferable to use zinc oxide.
- a catalyst used when preparing a polyvalent metallic salt of salicylic acids and a polyvalent metallic salt of rosin-modified phenolic resin which are used in the above-mentioned color developers for instance, inorganic ammonium salts such as ammonium carbonate and ammonium bicarbonate, alkali hydroxides such as sodium hydroxide, potassium hydroxide, and the like are exemplified.
- the used amount of the catalyst cannot be absolutely determined, but is usually 0.05 to 1.0 equivalent, preferably 0.1 to 0.4 equivalent per one equivalent of a metal in the polyvalent metallic compound. When the used amount of the catalyst is so smaller than 0.05 equivalent, it takes a long time for the reaction, and when the used amount is so greater than 0.1 equivalent, there is no meaning and it comes to be merely economically disadvantageous.
- a solvent used in the above-mentioned reaction for instance, eters, ketones, acetic acid esters and the like can be exemplified.
- the reaction temperature is usually 40° to 100°C, preferably 60° to 80°C.
- the reaction time is 1 to 6 hours.
- a polyvalent metallic salt of salicylic acid and a polyvalent metallic salt of a rosin-modified phenolic resin which are color developing components in the present invention are prepared by filtration and distrillation of a resulting product to remove unreacted inorganic compounds and a solvent from the product.
- the color developer of the present invention is a mixture of a polyvalent metallic salt of salicylic acids and a polyvalent metallic salt of a rosin-modified phenolic resin as mentioned above.
- the ratio of them is not particularly limited.
- the amount of the latter, i.e. the polyvalent metallic salt of a rosin-modified phenolic resin is usually adjusted to 0.1 to 100 parts by weight or so, preferably 0.1 to 50 parts by weight, more preferably 0.1 to 10 parts weight based upon 100 parts by weight of the former, i.e. the polyvalent metallic salt of salicylic acids.
- a method for coating the obtained color developer onto a substrate for a recording medium there is no limitation as to a method for coating the obtained color developer onto a substrate for a recording medium, and known methods can be adopted as they are. That is, for instance, various known methods such as a method for coating an aqueous paint, in which aqueous dispersion of the color developer is used, onto a substrate such as paper; a method for applying the color developer during paper sheet formation; a method for coating a solution or dispersion, which is prepared by mixing the color developer with an organic solvent, onto the surface of a substrate and drying it can be adopted.
- a wet grinding method comprising using a water soluble polymer such as polyvinyl alcohol, sodium polyacrylate or sodium polystyrenesulfonate as a dispersing agent, adding the color developer of the present invention into the aqueous solution of the dispersing agent and wet grinding them by means of Kady mill, sand mill, ball mill or the like to give a dispersion
- a method comprising dissolving the color developer in a suitable solvent, adding a protective colloid of polyvinyl alcohol carboxymethyl cellulose, ethylene-maleic anhydride copolymer or the like, water and if necessary, a suitable emulsifier, mechanically emulsifying them by means of a homogenizer and distilling an organic solvent from them under reduced pressure as occasion demands to give a dispersion, and the like can be adopted, and thereby improvement of waterproofness of printing which is the purpose of the present invention can be achieved.
- a water soluble polymer such as polyvinyl alcohol, sodium polyacrylate
- the method for preparing the aqueous dispersion of the present invention has been developed in order to improve storage stability of the aqueous dispersion.
- the storage stability is remarkably improved by mechanically emulsifying the color developer of the present invention in the coexistence of a specific dispersing agent, i.e. amorphous oligomer and polyvinyl alcohol.
- amorphous oligomer for instance, rosin ester, terpene resin, terpenephenolic resin, aromatically modified terpene resin, petroleum resin, hydrogenated petroleum resin, hydrogenated terpene resin, and the like are exemplified, and the amorphous oligomer is selected from one or more of them and used. Among them, it is preferable to use rosin ester and hydrogenated petroleum resin. It is preferable that the polyvinyl alcohol has an average polymerization degree of 100 to 2400 and a saponification value of 80 to 90 % by mole.
- the used amount of the amorphous oligomer is 10 to 100 % by weight, preferably 20 to 50 % by weight of a polyvalent metallic salt compound.
- the used amount of the polyvinyl alcohol is 1 to 30 % by weight, preferably 1 to 10 % by weight of solid components of the color developer and the amorphous oligomer to be emulsified.
- emulsifying known emulsifier and the like can be added thereto within a range that physical properties of the aqueous solution of the color developer are not impared.
- the method comprises the steps of dissolving the above-mentioned color developer in a suitable solvent such as ketones such as methyl ethyl ketone and methyl isobutyl ketone, acetic acid esters such as ethyl acetate and butyl acetate, and aromatic hydrocarbon solvents such as toluene and xylene; adding polyvinyl alcohol and water thereto and pre-emulsifying them sufficiently while keeping the temperature constantly to a range of 30° to 80°C; emulsifying and dispersing them with a homogenizer; and removing a solvent from them by distillation under reduced pressure to give a purposed aqueous dispersion of the color developer.
- a suitable solvent such as ketones such as methyl ethyl ketone and methyl isobutyl ketone, acetic acid esters such as ethyl acetate and butyl acetate, and aromatic hydrocarbon solvents such as toluene and xy
- a paint having a suitable viscosity and coating properties is prepared by properly mixing the aqueous dispersion prepared by the above-mentioned method with kaoline, calcium carbonate, starch, synthetic or natural latex, and the like.
- the content of the color developer in the paint is 5 to 60 % by weight, preferably 5 to 20 % by weight of the total amounts of solid components. When the content is less than 5 % by weight, color-forming properties are not sufficiently exhibited, and when the content exceeds 60 % by weight, there is a tendency that characteristics of paper of a color developing paper deteriorate.
- the amount of the color developer coated on a substrate such as paper is adjusted to 0.1 to 3.0 g/m2, preferably 0.2 to 0.7 g/m2 n a dry state.
- a lower paper can be prepared by applying the color developer of the present invention in accordance with the above-mentioned method.
- a capsule can be produced by dissolving various known color couplers such as triallylmethane compounds, diphenylmethane compounds, xanthene compounds, thiazine compounds, spiropyran compounds in a solvent such as an aliphatic hydrocarbon such as alkylnaphthalene, alkylated diphenylalkane, alkylated triphenyldimethane or alkylated diphenyl, kerosene, chlorinated diphenyl, chlorinated paraffin, cotton seed oil, linseed oil or soya bean oil in a known method for producing a capsule.
- a solvent such as an aliphatic hydrocarbon such as alkylnaphthalene, alkylated diphenylalkane, alkylated triphenyldimethane or alkylated diphenyl, kerosene, chlorinated diphenyl, chlorinated paraffin, cotton seed oil, linseed oil or soya bean oil
- a method for producing a capsule for instance, a method for producing a capsule in which coacervation is used, disclosed in USP 2,800,457 and U.S. Patent No. 2,800,458; a method for producing a capsule in which interfacial polymerization method is used, disclosed in U.K. Patent No. 990,443 and U.S. Patent No. 3,287,154; a method for producing a capsule in which precipitate of polymer is used, disclosed in U.S. Patent No. 3,418,250, U.S. Patent No. 3,660,304 and the like; a method for producing a capsule in which polymerization method of a reactant from the inner part of a drop of oil, disclosed in U.S. Patent No. 3,726,804 and U.S. Patent No. 3,796,669; and the like are exemplified.
- a flask equipped with an agitator, a Liebig-Graham condenser and a temperature gauge was charged with 1000 part of gum rosin, 1000 parts of carbolic acid and 0.7 part of paratoluenesulfonic acid as a catalyst, and the temperature was raised to 150° to 170°C.
- the reaction was carried out at the same temperature for 5 hours, and further the temperature was raised to 250° to 260°C while the carbolic acid was distilled off to give about 1250 parts of rosin-phenol addition reaction product.
- the product had an acid value of 107 and a softening point of 110°C.
- a reactor which is the same as that used in Preparation Example 1 was charged with 1000 parts of gun rosin, 1000 parts of carbolic acid and 0.6 part of paratoluenesulfonic acid as a catalyst, and the temperature was raised to 150° to 170°C. The reaction was carried out at the same temperature for 7 hours. After that, the temperature was decreased to about 100°C, and 2.7 parts of 5 % aqueous solution of lithium hydroxide was added thereto to carry out the neutralization of paratoluenesulfonic acid.
- the temperature was rasied to 290° to 300°C while unreacted carbolic acid was distilled off, and the polymerization reaction was carried out at the same temperature for 5 hours to give about 920 parts of rosin-phenol addition reaction product.
- the product had an acid value of 55 and a softening point of 150°C.
- a flask equipped with an agitator, a Liebig-Graham condenser and a temperature gauge was charged with 1000 parts of zinc 3,5-di-( ⁇ -methylbenzyl)salicylate and 50 parts of zinc salt of rosin-modified phenolic resin obtained in Preparation Example 1, and they were melted and mixed together at 180°C with stirring to give about 1050 parts of a color developer.
- Example 2 The same procedure of Example 1 was repeated except that 50 parts of zinc salt of rosin-modified phenolic resin obtained in Preparation Example 2 was used instead of 50 parts of the zinc salt of rosin-modified phenolic resin obtained in Preparation Example 1 to give about 1050 parts of a color developer.
- Example 2 The same procedure of Example 1 was repeated except that 1000 parts of zinc 3,5-di-tertiallybutylsalicylate was used instead of 1000 parts of zinc 3,5-di-( ⁇ -methylbenzyl)salicylate to give about 1050 parts of a color developer.
- Example 2 The same procedure of Example 1 was repeated except that the used amount of the zinc salt of rosin-modified phenolic resin was changed to 500 parts to give about 1500 parts of a color developer.
- Example 2 To 30 parts of the color developer obtained in Example 1, 15 parts of 10 % aqueous solution of sodium polyacrylate was added, and they were subjected to wet grinding by means of a ball mill for 24 hours to give a dispersion. To 5 parts of the dispersion, 22.5 parts of 50 % calcium carbonate slurry and 3.1 parts of styrenebutadiene latex (content of non-volatile components 48 %) were added, and they were kneaded for 90 minutes by means of a paint shaker to give a paint. The obtained paint was applied to a woodfree paper by means of a bar coater so that the weight of solid component was 5 g/m2 to give a color developing sheet.
- Example 5 The same procedure of Example 5 was repeated except that 30 parts of the color developer obtained in Example 2, 3 or 4 was used instead of 30 parts of the color developer obtained in Example 1 to give a color developing sheet.
- Example 2 The same procedure of Example 1 was repeated except that the amount of the zinc salt of rosin-modified phenolic resin was changed from 50 parts to 1500 parts to give about 2500 parts of a color developer for comparison.
- Example 5 the same procedure of Example 5 was repeated except that 30 parts of the above color developer for comparison was used instead of 30 parts of the color developer obtained in Example 1 to give a color developing sheet.
- Example 5 The same procedure of Example 5 was repeated except that 30 parts of zinc 3,5-di-tertiallybutyl-salicylate was used instead of 30 parts of the color developer obtained in Example 1 to give a color developing sheet.
- Example 5 The same procedure of Example 5 was repeated except that 30 parts of zinc 3,5-di-( ⁇ -methylbenzyl)salicylate was used instead of 30 parts of the color developer obtained in Example 1 to give a color developing sheet.
- an aqueous dispersion of the color developer improved in initial color-forming properties and waterproofness which have been the defects of conventional color developers for pressure-sensitive recording medium of polyvalent metallic salt of salicylic acids, can be prepared. Since in the color developer for pressure-sensitive recording medium of the present invention, inexpensive rosin-modified phenolic resin is used as a starting material, production cost is markedly decreased.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Color Printing (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP78986/89 | 1989-03-29 | ||
JP1078986A JPH02255375A (ja) | 1989-03-29 | 1989-03-29 | 感圧記録体用顕色剤、顕色剤の水性分散液およびその製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0419659A1 true EP0419659A1 (de) | 1991-04-03 |
EP0419659A4 EP0419659A4 (en) | 1991-07-03 |
Family
ID=13677217
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19890907826 Withdrawn EP0419659A4 (en) | 1989-03-29 | 1989-06-30 | Color developer for pressure-sensitive recording medium, aqueous dispersion of color developer, and process for its preparation |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0419659A4 (de) |
JP (1) | JPH02255375A (de) |
AU (1) | AU615319B2 (de) |
WO (1) | WO1990011190A1 (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005040242A1 (fr) * | 2003-10-29 | 2005-05-06 | Zonglai Liu | Composition de resine a developpant de couleur, emulsion et processus de preparation de celle-ci |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0218810A2 (de) * | 1985-07-19 | 1987-04-22 | Jujo Paper Co., Ltd. | Farbentwicklungsmittel für druckempfindliches Aufzeichnungsblatt und Farbentwicklungsblatt dafür |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU560131B2 (en) * | 1977-12-02 | 1987-04-02 | Barry, Graham Charles | Invisible ink structure |
AU539032B2 (en) * | 1978-12-29 | 1984-09-06 | Appleton Papers Inc. | Furo(3,4-b) pyridin-5-(7)-one derivatives |
AU521189B2 (en) * | 1979-11-22 | 1982-03-18 | Mitsubishi Paper Mills Ltd. | Colour developing sheet for no-carbon copying process |
JPS56139991A (en) * | 1980-04-01 | 1981-10-31 | Mitsubishi Paper Mills Ltd | Developer sheet for no-carbon duplicating paper |
JPS58122891A (ja) * | 1982-01-14 | 1983-07-21 | Takahashi Ink Kagaku Kogyosho:Kk | 顕色インキ |
JPS59174384A (ja) * | 1983-03-24 | 1984-10-02 | Mitsubishi Paper Mills Ltd | 画像記録材料 |
JPS63176176A (ja) * | 1987-01-16 | 1988-07-20 | Jujo Paper Co Ltd | 感圧複写紙用顕色シ−ト |
JPH0520807A (ja) * | 1991-07-12 | 1993-01-29 | Matsushita Electric Ind Co Ltd | フロツピーデイスク装置 |
JPH0799968B2 (ja) * | 1991-12-24 | 1995-11-01 | 神奈川県 | 培地挿入式自動播種装置 |
-
1989
- 1989-03-29 JP JP1078986A patent/JPH02255375A/ja active Pending
- 1989-06-30 WO PCT/JP1989/000658 patent/WO1990011190A1/ja not_active Application Discontinuation
- 1989-06-30 EP EP19890907826 patent/EP0419659A4/en not_active Withdrawn
- 1989-06-30 AU AU38552/89A patent/AU615319B2/en not_active Ceased
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0218810A2 (de) * | 1985-07-19 | 1987-04-22 | Jujo Paper Co., Ltd. | Farbentwicklungsmittel für druckempfindliches Aufzeichnungsblatt und Farbentwicklungsblatt dafür |
Non-Patent Citations (1)
Title |
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See also references of WO9011190A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO1990011190A1 (en) | 1990-10-04 |
AU615319B2 (en) | 1991-09-26 |
EP0419659A4 (en) | 1991-07-03 |
AU3855289A (en) | 1990-10-22 |
JPH02255375A (ja) | 1990-10-16 |
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