EP0111564A1 - Color-developing sheet for pressure-sensitive recording - Google Patents
Color-developing sheet for pressure-sensitive recording Download PDFInfo
- Publication number
- EP0111564A1 EP0111564A1 EP83901395A EP83901395A EP0111564A1 EP 0111564 A1 EP0111564 A1 EP 0111564A1 EP 83901395 A EP83901395 A EP 83901395A EP 83901395 A EP83901395 A EP 83901395A EP 0111564 A1 EP0111564 A1 EP 0111564A1
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- European Patent Office
- Prior art keywords
- color
- compound
- clay mineral
- acid
- developing
- 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.)
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- -1 aluminum compound Chemical class 0.000 claims abstract description 18
- 239000011973 solid acid Substances 0.000 claims abstract description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000002734 clay mineral Substances 0.000 claims abstract description 13
- 150000003752 zinc compounds Chemical class 0.000 claims abstract description 10
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000002253 acid Substances 0.000 claims abstract description 8
- 239000011777 magnesium Substances 0.000 claims abstract description 8
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 8
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 5
- 238000001035 drying Methods 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims abstract description 5
- 239000002609 medium Substances 0.000 claims abstract description 4
- 239000003513 alkali Substances 0.000 claims abstract description 3
- 239000012736 aqueous medium Substances 0.000 claims abstract description 3
- 230000003472 neutralizing effect Effects 0.000 claims abstract description 3
- 150000002681 magnesium compounds Chemical class 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 6
- 239000004615 ingredient Substances 0.000 abstract 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 230000014759 maintenance of location Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 150000002989 phenols Chemical class 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- MOZDKDIOPSPTBH-UHFFFAOYSA-N Benzyl parahydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OCC1=CC=CC=C1 MOZDKDIOPSPTBH-UHFFFAOYSA-N 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000013808 oxidized starch Nutrition 0.000 description 2
- 239000001254 oxidized starch Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- CVNOWLNNPYYEOH-UHFFFAOYSA-N 4-cyanophenol Chemical compound OC1=CC=C(C#N)C=C1 CVNOWLNNPYYEOH-UHFFFAOYSA-N 0.000 description 1
- DIRCLGLKRZLKHG-UHFFFAOYSA-N 4-hydroxybenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=C(O)C=C1 DIRCLGLKRZLKHG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000002524 electron diffraction data Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000011092 plastic-coated paper Substances 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- PCHQDTOLHOFHHK-UHFFFAOYSA-L zinc;hydrogen carbonate Chemical compound [Zn+2].OC([O-])=O.OC([O-])=O PCHQDTOLHOFHHK-UHFFFAOYSA-L 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
- B41M5/124—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
- B41M5/1555—Inorganic mineral developers, e.g. clays
Definitions
- This invention relates to a color-developing sheet having a novel constitution for pressure-sensitive recording.
- the pressure-sensitive recording material comprises usually a color-forming sheet having an electron-donative leuco dye on the surface and a color-developing sheet having a color developer, which is electron attractive, on the surface.
- a color-forming reaction based on electron transfer is utilized for recording by bringing both the surfaces into contact with each other and applying printing pressure thereto.
- the color developer is one of the principal components of this recording material.and various color developers have hitherto been proposed.
- activated clay which is obtained by treating a natural clay mineral with acid to a slight or medium extent, phenol compounds, phenolic resins of novolak type, and metal salts of aromatic carboxylic acids.
- Activated clay first mentioned which is the oldest of the above color developers, is insufficient in an essential property, i.e. the color developing ability. Hence, there are cases where activated clay has been replaced with some of the above-mentioned organic color developers.
- a clay mineral having a layer structure build up of regular tetrahedrons of silica is treated with an acid so as to give a silica content of 82 - 96.5% by weight on a dry basis (dried at 105°C for 3 hours);
- a magnesium component and/or aluminum component is introduced into the acid-treated clay mineral by bringing it, in an aqueous medium, into contact with a magnesium compound and/or aluminum compound soluble at least partially in the medium and if this soluble compound is other than the hydroxide, by neutralizing it with alkali or acid to form the hydroxide; and if desired, the resulting clay mineral is dried (hereinafter this color developer is referred to as "semi-synthetic solid acid").
- the semi-synthetic solid acid can be regarded as a new type of color developer capable of offsetting sufficiently drawbacks of conventional activated clays and expected to be comparable or superior in the color developing ability to organic color developers.
- the present inventors evaluated by various tests the aptitude of the semi-synthetic solid acid, which is a new type of inorganic color developer prepared in the above process, for use in the color-developing layer for pressure-sensitive recording. As a result, a marked improvement in the color developing ability and a good retention of the colored image density under high humidity conditions were surely recognized and hence distinct differences were observed between this semi-synthetic solid acid and the clay mineral group color developer so far known and used. On the other hand, it was found as a drawback of the semi-synthetic solid acid that some fastness, for example, light fastness, of the color image formed in the color-developing layer employing the semi-synthetic solid acid is rather deteriorated.
- the phenol compound used jointly with the semi-synthetic solid acid in this invention may be either a low molecular weight phenol compound or a phenolic resin.
- suitable phenol compounds which do not cause such a side reaction as the discoloration or coloration of the blank areas or the degradation are, for example, alkyl, aralkyl, or aryl p-hydroxybenzoates, p-hydroxybenzonitrile, p-hydroxybenzenesulfonamide, 4-hydroxybenzophenone, 2,4-dihydroxybenzophenone, dialkyl, diaralkyl, or diaryl 4-hydroxyphthalic acid esters, and various hindered phenols. Suitable amounts thereof used are 1-100 parts per 100 parts of the semi-synthetic solid acid.
- Especially effective zinc compounds used in this invention are, for example, zinc oxide, zinc hydroxide, zinc carbonate, basic zinc carbonate, zinc sulfide, zinc phosphate, and zinc salts of various organic acids. Suitable amounts thereof used are 1-100 parts per 100 parts of the semi-synthetic solid acid.
- the semi-synthetic solid acid used in this invention is derived from a clay mineral having a layer structure build up of regular tetrahedrons of silica, and this color developer for pressure-sensitive copying paper is featured by
- Preferred examples of the above color developer for pressure-sensitive copying paper used in this invention satisfy the above conditions (A), (B), and (C) and additionally the condition that (D) the atomic ratio of [silicon]/[the sum of magnesium and/or aluminum] therein is 12/1.5 - 12/12, particularly 12/3 - 12/10.
- the sum of magnesium and/or aluminum in the above atomic ratio means the amount of the contained one.
- the combined use of the semi-synthetic solid acid, phenol compound, and zinc compound gives a color-developing sheet for pressure-sensitive recording materials which is far more improved in the fastness of the color image than does the use of the semi-synthetic solid acid alone.
- the simultaneous addition of the phenol compound and zinc compound has excellent effects particularly in improving the fastness of the color image formed as compared with the separate addition of the compounds. That is, a synergistic effect is observed in the former case.
- the color-developing layer for pressure-sensitive recording is formed by; mixing the semi-synthetic solid acid, one or more of the zinc compounds, one or more of the phenol compounds, a binder, a dispersant, some other additive, and if desired, a pigment such as clay, kaolin, satin white, calcium carbonate, titanium white, magnesium oxide, talc, alumina, aluminum hydroxide, urea resin pigment, or plastic pigment; applying the resulting coating liquid on a sheet-like support such as paper, plastic film, plastic-coated paper, or the like by using an air knife coater, blade coater, roll coater, flexo coater, gravure coater, rubber doctor coater, curtain coater, or some other coating means; and drying the coat.
- a pigment such as clay, kaolin, satin white, calcium carbonate, titanium white, magnesium oxide, talc, alumina, aluminum hydroxide, urea resin pigment, or plastic pigment
- the color developing layer in this invention is formed by using the semi-synthetic solid acid as color developer and using cojointly the zinc compound and the phenol compound.
- this invention has been successful in providing a pressure-sensitive recording system unprecedentedly markedly improved in all the color forming rate, formed color density, fastness of the formed color image (to light, water, humidity, plasticizer, oxidizing gas, etc.), and stability (retention of color developing ability, resistance to yellowing) of the image-less areas (blank areas).
- the formed color density, the retention thereof under high humidity conditions, and the fastness of the formed color image to NOx are improved, the fading with light is reduced, and the blank areas do not undergo the yellowing.
- samples were prepared without adding either benzyl p-hydroxybenzoate or zinc oxide (sample A), without adding benzyl p-hydroxybenzoate but with adding the same amount of zinc oxide (sample C), and without adding zinc oxide but with adding the same amount of benzyl p-hydroxybenzoate (sample B) were prepared in the same manner as the above.
- Color-forming sheets (CB) herein used were prepared as follows: A solution of electron-donative leuco dyes in a high boiling solvent having the composition:
- micro-capsuled with a melamine resin according to the method of U.S. Patent No. 4,233,178.
- To 100 parts (dry basis) of the micro-capsules were added 25 parts of wheat starch and 150 parts of a 10% aqueous solution of oxidized starch.
- the resulting mixture was coated on 40-g/m 2 base paper to give a dry coating weight of 5 g/m 2 .
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Color Printing (AREA)
Abstract
Description
- This invention relates to a color-developing sheet having a novel constitution for pressure-sensitive recording.
- The pressure-sensitive recording material comprises usually a color-forming sheet having an electron-donative leuco dye on the surface and a color-developing sheet having a color developer, which is electron attractive, on the surface. In this recording material, a color-forming reaction based on electron transfer is utilized for recording by bringing both the surfaces into contact with each other and applying printing pressure thereto.
- Accordingly, the color developer is one of the principal components of this recording material.and various color developers have hitherto been proposed. For example, there have been proposed activated clay, which is obtained by treating a natural clay mineral with acid to a slight or medium extent, phenol compounds, phenolic resins of novolak type, and metal salts of aromatic carboxylic acids.
- Activated clay first mentioned, which is the oldest of the above color developers, is insufficient in an essential property, i.e. the color developing ability. Hence, there are cases where activated clay has been replaced with some of the above-mentioned organic color developers.
- On the other hand, a novel color developer has been proposed recently which is prepared by a semi-synthetic process (Japanese Patent Application Kokai No. 15996/82).
- It is a color developer for use in pressure-sensitive recording materials which is prepared in the following way: A clay mineral having a layer structure build up of regular tetrahedrons of silica is treated with an acid so as to give a silica content of 82 - 96.5% by weight on a dry basis (dried at 105°C for 3 hours); a magnesium component and/or aluminum component is introduced into the acid-treated clay mineral by bringing it, in an aqueous medium, into contact with a magnesium compound and/or aluminum compound soluble at least partially in the medium and if this soluble compound is other than the hydroxide, by neutralizing it with alkali or acid to form the hydroxide; and if desired, the resulting clay mineral is dried (hereinafter this color developer is referred to as "semi-synthetic solid acid"). This technique has brought about an improvement in the color-developing ability for electron-donative leuco dyes, long lasting of the color-developing effect under high humidity conditions, and less decay with time of the formed color density. Thus, the semi-synthetic solid acid can be regarded as a new type of color developer capable of offsetting sufficiently drawbacks of conventional activated clays and expected to be comparable or superior in the color developing ability to organic color developers.
- The present inventors evaluated by various tests the aptitude of the semi-synthetic solid acid, which is a new type of inorganic color developer prepared in the above process, for use in the color-developing layer for pressure-sensitive recording. As a result, a marked improvement in the color developing ability and a good retention of the colored image density under high humidity conditions were surely recognized and hence distinct differences were observed between this semi-synthetic solid acid and the clay mineral group color developer so far known and used. On the other hand, it was found as a drawback of the semi-synthetic solid acid that some fastness, for example, light fastness, of the color image formed in the color-developing layer employing the semi-synthetic solid acid is rather deteriorated.
- In view of the above, the present inventors made extensive studies in the search for a means of improving the fastness of the color image formed in such a color-developing layer. As a result, this invention has been accomplished through new finding that the addition of any of various known antioxydants such as aromatic amines and hindered phenols and any of ultraviolet absorbers such as benzotriazole derivatives is little effective, but the addition of necessary amounts of a phenol compound and a zinc compound markedly improves the light fastness of the color image formed; in particular the use of a selected phenol compound together with a zinc compound gives a semi-synthetic solid acid-containing color-developing layer really excellent in practical use which does not cause any objectionable side reaction such as the yellowing of the blank areas (image-less areas on the color-developing layer).
- The phenol compound used jointly with the semi-synthetic solid acid in this invention may be either a low molecular weight phenol compound or a phenolic resin. Especially suitable phenol compounds which do not cause such a side reaction as the discoloration or coloration of the blank areas or the degradation are, for example, alkyl, aralkyl, or aryl p-hydroxybenzoates, p-hydroxybenzonitrile, p-hydroxybenzenesulfonamide, 4-hydroxybenzophenone, 2,4-dihydroxybenzophenone, dialkyl, diaralkyl, or diaryl 4-hydroxyphthalic acid esters, and various hindered phenols. Suitable amounts thereof used are 1-100 parts per 100 parts of the semi-synthetic solid acid.
- Especially effective zinc compounds used in this invention are, for example, zinc oxide, zinc hydroxide, zinc carbonate, basic zinc carbonate, zinc sulfide, zinc phosphate, and zinc salts of various organic acids. Suitable amounts thereof used are 1-100 parts per 100 parts of the semi-synthetic solid acid.
- The semi-synthetic solid acid used in this invention is derived from a clay mineral having a layer structure build up of regular tetrahedrons of silica, and this color developer for pressure-sensitive copying paper is featured by
- (A) indicating an electron diffraction pattern based on the crystals of the above layer structure built up of regular tetrahedrons of silica,
- (B) indicating no X-ray diffraction pattern based on the above layer structure, and
- (C) containing at least silicon and magnesium and/or aluminum as elements besides oxygen.
- Preferred examples of the above color developer for pressure-sensitive copying paper used in this invention satisfy the above conditions (A), (B), and (C) and additionally the condition that
(D) the atomic ratio of [silicon]/[the sum of magnesium and/or aluminum] therein is 12/1.5 - 12/12, particularly 12/3 - 12/10. Herein, when only one of magnesium and aluminum is contained, the sum of magnesium and/or aluminum in the above atomic ratio means the amount of the contained one. - As stated above, it has been found in this invention that the combined use of the semi-synthetic solid acid, phenol compound, and zinc compound gives a color-developing sheet for pressure-sensitive recording materials which is far more improved in the fastness of the color image than does the use of the semi-synthetic solid acid alone. Moreover, as will be shown later in Examples, the simultaneous addition of the phenol compound and zinc compound has excellent effects particularly in improving the fastness of the color image formed as compared with the separate addition of the compounds. That is, a synergistic effect is observed in the former case.
- In this invention, the color-developing layer for pressure-sensitive recording is formed by; mixing the semi-synthetic solid acid, one or more of the zinc compounds, one or more of the phenol compounds, a binder, a dispersant, some other additive, and if desired, a pigment such as clay, kaolin, satin white, calcium carbonate, titanium white, magnesium oxide, talc, alumina, aluminum hydroxide, urea resin pigment, or plastic pigment; applying the resulting coating liquid on a sheet-like support such as paper, plastic film, plastic-coated paper, or the like by using an air knife coater, blade coater, roll coater, flexo coater, gravure coater, rubber doctor coater, curtain coater, or some other coating means; and drying the coat.
- As described above, the color developing layer in this invention is formed by using the semi-synthetic solid acid as color developer and using cojointly the zinc compound and the phenol compound. In this way, this invention has been successful in providing a pressure-sensitive recording system unprecedentedly markedly improved in all the color forming rate, formed color density, fastness of the formed color image (to light, water, humidity, plasticizer, oxidizing gas, etc.), and stability (retention of color developing ability, resistance to yellowing) of the image-less areas (blank areas). In particular, it is noteworthy that the formed color density, the retention thereof under high humidity conditions, and the fastness of the formed color image to NOx are improved, the fading with light is reduced, and the blank areas do not undergo the yellowing.
- Referring now to a typical example, preferred embodiments of this invention are illustrated in more detail. In the following example, "parts" are all by weight.
- The following mixture was ball-milled for two days.
-
- Then, 100 parts of a semi-synthetic solid acid (tradename: Silton SS-1, mfd. by Mizusawa Chem. Ind. Co., Ltd.),
- 10 parts of zinc oxide, and 50 parts of the above dispersion of benzyl p-hydroxybenzoate prepared by the wet grinding were dispersed in 200 parts of water dissolving 1 part of sodium pyrophosphate. To the resulting dispersion were added 50 parts of a 10% aqueous solution of oxidized starch and 50 parts of a 48% SBR latex to prepare a coating liquid. It was coated on 40-g/m2 base paper to give a dry coating weight of 4.5 g/m2. Thus, color-developing sheets (CF) were prepared (sample D).
- For the purpose of comparative tests, samples were prepared without adding either benzyl p-hydroxybenzoate or zinc oxide (sample A), without adding benzyl p-hydroxybenzoate but with adding the same amount of zinc oxide (sample C), and without adding zinc oxide but with adding the same amount of benzyl p-hydroxybenzoate (sample B) were prepared in the same manner as the above.
-
- was micro-capsuled with a melamine resin according to the method of U.S. Patent No. 4,233,178. To 100 parts (dry basis) of the micro-capsules were added 25 parts of wheat starch and 150 parts of a 10% aqueous solution of oxidized starch. The resulting mixture was coated on 40-g/m2 base paper to give a dry coating weight of 5 g/m2.
- A specimen of each of the thus obtained CF sheets (4 types) and a specimen of the CB sheets were superposed so as to oppose the coating surfaces and were super- calendered. After one or more days, tests of exposure to sunlight and room scattered light and other fastness tests were conducted on the thus colored specimens of the color-developing sheets (Table 1).
- From Table 1, a synergy is observed in the effect of this invention. In other words, when (the retentions of the samples B, C, and D) (%) - (the retention of the sample A) (%) are designated as ΔB, ΔC, and ΔD(%) in the sunlight exposure tests, ΔB = 11(%), ΔC = 2(%), and ΔD = 23(%) and therefore ΔD > ΔB + ΔC.
- The same relations are found in the NOx exposure, room scattered light exposure, and plasticizer exposure test results.
- Thus, according to this invention, much greater improvements in the fastness of the color image have been attained by combined use of the phenol compound and the zinc compound than by separate use of these compounds.
Claims (1)
- A color-developing sheet for pressure-sensitive recording, characterized in that the color-developing layer of the sheet contains (a) a semi-synthetic solid acid prepared by (1) treating a clay mineral which has a layer structure built up of regular tetrahedrons of silica, with an acid so as to give a silica content of 82 - 96.5% by weight on a dry basis (drying at 105°C for 3 hours), (2) bringing the resulting clay mineral, in an aqueous medium, into contact with a magnesium compound and/or aluminum compound soluble at least partially in the medium and if this soluble compound is other than the hydroxide, neutralizing it with alkali or acid to form the hydroxide, thus introducing a magnesium component and/or alumihum component into the acid-treated clay mineral, and (3) if desired, drying the resulting clay mineral, (B) a phenol compound, and (C) a zinc compound.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57107022A JPS58222880A (en) | 1982-06-22 | 1982-06-22 | Color developing layer for pressure-sensitive recording |
JP107022/82 | 1982-06-22 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0111564A1 true EP0111564A1 (en) | 1984-06-27 |
EP0111564A4 EP0111564A4 (en) | 1984-09-28 |
EP0111564B1 EP0111564B1 (en) | 1987-09-09 |
Family
ID=14448524
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP83901395A Expired EP0111564B1 (en) | 1982-06-22 | 1983-05-04 | Color-developing sheet for pressure-sensitive recording |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0111564B1 (en) |
JP (1) | JPS58222880A (en) |
AU (1) | AU1518383A (en) |
DE (1) | DE3373441D1 (en) |
WO (1) | WO1984000131A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0134818A1 (en) * | 1983-01-26 | 1985-03-27 | Mitsubishi Paper Mills, Ltd. | No carbon required paper for letter printer |
EP0160106A1 (en) * | 1983-10-31 | 1985-11-06 | Mitsubishi Paper Mills, Ltd. | Process for manufacturing color-developing sheet for image-recording material |
WO1995005422A1 (en) * | 1993-08-12 | 1995-02-23 | Süd-Chemie AG | Process for producing neutral to alkaline dye coupling developer pigments |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0044645A1 (en) * | 1980-07-03 | 1982-01-27 | Mizusawa Kagaku Kogyo Kabushiki Kaisha | Novel clay mineral color developer for pressure sensitive recording paper and process for producing same |
EP0105376A1 (en) * | 1982-03-03 | 1984-04-18 | Mitsubishi Paper Mills, Ltd. | Color-developing sheet for use in no-carbon recording system |
-
1982
- 1982-06-22 JP JP57107022A patent/JPS58222880A/en active Granted
-
1983
- 1983-05-04 AU AU15183/83A patent/AU1518383A/en not_active Abandoned
- 1983-05-04 DE DE8383901395T patent/DE3373441D1/en not_active Expired
- 1983-05-04 EP EP83901395A patent/EP0111564B1/en not_active Expired
- 1983-05-04 WO PCT/JP1983/000137 patent/WO1984000131A1/en active IP Right Grant
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0044645A1 (en) * | 1980-07-03 | 1982-01-27 | Mizusawa Kagaku Kogyo Kabushiki Kaisha | Novel clay mineral color developer for pressure sensitive recording paper and process for producing same |
EP0105376A1 (en) * | 1982-03-03 | 1984-04-18 | Mitsubishi Paper Mills, Ltd. | Color-developing sheet for use in no-carbon recording system |
Non-Patent Citations (2)
Title |
---|
No further relevant documents disclosed * |
See also references of WO8400131A1 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0134818A1 (en) * | 1983-01-26 | 1985-03-27 | Mitsubishi Paper Mills, Ltd. | No carbon required paper for letter printer |
EP0134818B1 (en) * | 1983-01-26 | 1991-03-13 | Mitsubishi Paper Mills, Ltd. | No carbon required paper for letter printer |
EP0160106A1 (en) * | 1983-10-31 | 1985-11-06 | Mitsubishi Paper Mills, Ltd. | Process for manufacturing color-developing sheet for image-recording material |
EP0160106A4 (en) * | 1983-10-31 | 1986-11-26 | Mitsubishi Paper Mills Ltd | METHOD OF MANUFACTURING A COLOR DEVELOPMENT SHEET FOR AN IMAGE RECORDING MATERIAL. |
WO1995005422A1 (en) * | 1993-08-12 | 1995-02-23 | Süd-Chemie AG | Process for producing neutral to alkaline dye coupling developer pigments |
US5637552A (en) * | 1993-08-12 | 1997-06-10 | Sud-Chemie A.G. | Process for producing neutral to alkali color developer pigments |
Also Published As
Publication number | Publication date |
---|---|
AU1518383A (en) | 1984-01-26 |
DE3373441D1 (en) | 1987-10-15 |
JPH0227956B2 (en) | 1990-06-20 |
EP0111564B1 (en) | 1987-09-09 |
WO1984000131A1 (en) | 1984-01-19 |
JPS58222880A (en) | 1983-12-24 |
EP0111564A4 (en) | 1984-09-28 |
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