EP0482409A1 - Kohlefreies Papier mit erhöhter Geschwindigkeit - Google Patents
Kohlefreies Papier mit erhöhter Geschwindigkeit Download PDFInfo
- Publication number
- EP0482409A1 EP0482409A1 EP9191117025A EP91117025A EP0482409A1 EP 0482409 A1 EP0482409 A1 EP 0482409A1 EP 9191117025 A EP9191117025 A EP 9191117025A EP 91117025 A EP91117025 A EP 91117025A EP 0482409 A1 EP0482409 A1 EP 0482409A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- image
- alkyl
- forming component
- composition
- carbonless
- 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- Withdrawn
Links
- 229920005989 resin Polymers 0.000 claims abstract description 33
- 239000011347 resin Substances 0.000 claims abstract description 33
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims abstract description 32
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims abstract description 26
- 239000000049 pigment Substances 0.000 claims abstract description 22
- 239000011230 binding agent Substances 0.000 claims abstract description 17
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229960004889 salicylic acid Drugs 0.000 claims abstract description 16
- 239000008199 coating composition Substances 0.000 claims abstract description 15
- 239000007859 condensation product Substances 0.000 claims abstract description 15
- 150000002989 phenols Chemical class 0.000 claims abstract description 15
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 12
- 239000002184 metal Substances 0.000 claims abstract description 12
- 230000003993 interaction Effects 0.000 claims abstract description 10
- 239000006185 dispersion Substances 0.000 claims abstract description 8
- 239000000758 substrate Substances 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 35
- 230000000295 complement effect Effects 0.000 claims description 23
- 238000012546 transfer Methods 0.000 claims description 18
- 239000003094 microcapsule Substances 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 239000002243 precursor Substances 0.000 claims description 11
- 238000011161 development Methods 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 238000003825 pressing Methods 0.000 claims 1
- 238000000576 coating method Methods 0.000 abstract description 15
- 238000003384 imaging method Methods 0.000 abstract description 8
- 239000011248 coating agent Substances 0.000 description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical group [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-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
- 238000013019 agitation Methods 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- -1 e.g. Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 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 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-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
- PVULMDLILHXVIO-UHFFFAOYSA-N 2-nonoxybenzoic acid Chemical compound CCCCCCCCCOC1=CC=CC=C1C(O)=O PVULMDLILHXVIO-UHFFFAOYSA-N 0.000 description 1
- ISAVYTVYFVQUDY-UHFFFAOYSA-N 4-tert-Octylphenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C=C1 ISAVYTVYFVQUDY-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 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
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- YLZSIUVOIFJGQZ-UHFFFAOYSA-N bis[4-(dimethylamino)phenyl]methanol Chemical compound C1=CC(N(C)C)=CC=C1C(O)C1=CC=C(N(C)C)C=C1 YLZSIUVOIFJGQZ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 description 1
- 239000003593 chromogenic compound Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- QTWZICCBKBYHDM-UHFFFAOYSA-N leucomethylene blue Chemical compound C1=C(N(C)C)C=C2SC3=CC(N(C)C)=CC=C3NC2=C1 QTWZICCBKBYHDM-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 235000013550 pizza Nutrition 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003870 salicylic acids Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000007581 slurry coating method Methods 0.000 description 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-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
Definitions
- the present invention relates to carbonless copying systems, and more specifically, to compositions for use with coated front (CF) paper, which compositions provide enhanced image development speed for carbonless paper at below room temperature.
- CF coated front
- Standard carbonless copying systems or pressure sensitive copying paper include a plurality of substrates, e.g., paper sheets, arranged in a manifold, each sheet having one or more coatings on a surface thereof.
- the manifold is designed so that when external pressure caused by a typewriter, pen, or other instrument is applied to the outermost sheet, a colored image will be formed on at least one surface of each sheet of the manifold.
- the top sheet of the manifold to which the pressure is applied has a coating on its back surface.
- This coated back surface typically includes microcapsules containing an initially colorless chemically reactive color-forming dye precursor as the fill material.
- the front surface of the next sheet, which is adjacent to the back surface of the top sheet, is coated with a material containing a component, such as phenolic resin or reactive clay, that is capable of reacting with the colorless dye precursor contained in the microcapsules to produce a color.
- a component such as phenolic resin or reactive clay
- the sheets of the carbonless copying system manifold are designated in the art by the terms CB for "coated back,” CFB for “coated front and back,” and CF for "coated front.”
- the CB or transfer sheet is usually the top sheet of the manifold and the sheet to which the external pressure is applied.
- the CFB sheets are the intermediate sheets of the manifold, each of which is able to have an image formed on its front surface by a pressure, and each of which also transmits the contents of ruptured microcapsules from its back surface to the front surface of the next sheet.
- the CF or recording sheet is the bottom sheet and is coated only on its front surface so that an image can be formed on it.
- the coating containing the microcapsules on the back surface of the sheets and to have the coating containing the reactive component for the capsules on the front surface of each of the sheets, the reverse arrangement is also possible.
- one of the reactive ingredients may be carried in the sheets themselves, rather than applied as surface coatings.
- the component that reacts with the colorless dye precursor may also be microencapsulated.
- a carbonless copying system CF coating incorporating a resin which is a phenol/aldehyde condensation product produced by the interaction of an alkyl-substituted salicylic acid, an alkyl-substituted phenol, an aldehyde and a metal source; along with a binder and a pigment; provides faster imaging than standard CF coatings which contain HRJ-2456, especially at temperatures below room temperature.
- the present invention provides a coating composition for use in carbonless copying systems.
- the composition comprises a phenol/aldehyde condensation product produced by the interaction of an alkyl-substituted salicylic acid, an alkyl-substituted phenol, an aldehyde and a metal source; a binder; and a pigment, wherein the composition is capable of providing enhanced image development at temperatures below 40°F.
- the present invention also provides a carbonless copying system comprising a recording substrate; a first image-forming component which is a mixture of (1) a phenol/aldehyde condensation product resin formed by the interaction of an alkyl-substituted salicylic acid, an alkyl-substituted phenol, an aldehyde and a metal source, (2) a binder, and (3) a pigment; and a complementary image-forming component, encapsulated in microcapsules and capable of reacting with the first image-forming component to produce a colored reaction product; the first image-forming component and the complementary image-forming component are arranged in juxtaposed contact with one another whereby the application of pressure in selected areas upon the carbonless system causes a colored image to form on corresponding areas of the recording substrate, wherein the system is capable of providing enhanced image development at temperatures below 40°F.
- a first image-forming component which is a mixture of (1) a phenol/aldehyde condensation product resin formed by the interaction of an alkyl-substi
- the present invention also provides a carbonless copying system comprising a recording substrate; a transfer substrate; a first image-forming component which is a mixture of (1) a phenol/aldehyde condensation product resin formed by the interaction of an alkyl-substituted salicylic acid, an alkyl-substituted phenol, an aldehyde and a metal source, (2) a binder, and (3) a pigment and is carried by the recording substrate; a complementary image-forming component encapsulated in microcapsules carried by the transfer substrate and capable of reacting with the first image-forming component to produce a colored reaction product; and the first image-forming component is arranged in juxtaposed contact with the complementary image-forming component whereby the application of pressure in selected areas upon the carbonless system causes colored images to form on corresponding areas of the recording substrate.
- the system is capable of providing enhanced image development at temperatures below 40°F.
- the present invention also provides a method of using the carbonless copy system of this invention at temperatures below room temperature, including temperatures below 40°F.
- a coating composition for use in carbonless copying systems.
- the composition comprises a resin which is a phenol/aldehyde condensation product produced by the interaction of an alkyl-substituted salicylic acid, an alkyl-substituted phenol, an aldehyde and a metal source; a binder; and a pigment.
- the coating composition is applied to a coated front (CF) sheet in a carbonless copying manifold.
- the alkyl-substituted salicylic acid is substituted with at least one alkyl group containing three or more carbon atoms. More preferably, the alkyl group contains at least four carbon atoms, even more preferably, four to twelve carbon atoms.
- Particularly useful are salicylic acids of the formula I: where R is an alkyl group containing from four to twelve carbon atoms.
- the group R is preferably octyl or nonyl, especially tertiary-octyl (derived from di-isobutene) and nonyl (derived from propylene trimer).
- the group R may also be a dodecyl group.
- the preferred group is the nonyl group.
- the alkylphenol component preferably contains at least one alkyl group containing at least three carbon atoms, more preferably, four to twelve carbon atoms.
- the phenols are phenols substituted in the para-position with an alkyl group containing four to twelve carbon atoms, particularly tertiary-butyl, tertiary-octyl, nonyl (derived from propylene trimer) and dodecyl.
- the preferred material is the tertiary-octyl group.
- the alkyl substituted group in the para position is represented by R' in formula II below.
- the aldehyde is preferably formaldehyde, although the formaldehyde may be supplied, for example, from paraformaldehyde or a similar source of formaldehyde.
- the preferred metal source is zinc oxide.
- the phenol/aldehyde condensation product may be synthesized by combining and heating the alkyl-substituted salicylic acid, the alkyl-substituted phenol, the aldehyde, the metal source and water.
- EPA 0,338,808 discloses a general example of a suitable manufacturing process: 750 parts nonylsalicylic acid, 523 parts p-t-octylphenol, 199 parts 50% formaldehyde solution, 3 parts of Daxad 30 (a wetting agent of proprietary composition available from W.R. Grace & Co.), 69 parts water and 103 parts of zinc oxide are heated to reflux with agitation. After the reaction takes place, heating is discontinued and additional wetting agent is added. The mixture is cooled with agitation, and further diluted with water. The mixture is then filtered to obtain the phenol/aldehyde condensation product.
- Daxad 30 a wetting agent of proprietary composition available from W.R. Grace & Co.
- the resin dispersion which is a component of the coating composition of the invention may be HRJ-10176 or HRJ-10802, which are trademark names of resins manufactured and supplied by Schenectady Chemicals, Inc. of Schenectady, New York. Applicant has been informed by Schenectady Chemicals, Inc. that HRJ-10176 and HRJ-10802 are each within the scope of the description and/or the claims of the phenol/aldehyde condensation product of EPA 0,338,808.
- the resin component of the coating composition of the invention is preferably present in an amount ranging from 7 to 40 parts, more preferably from 10 to 20 parts, per 100 parts of the pigment and resin. Unless otherwise stated, "parts" in this invention are parts by weight.
- the pigment component of the coating composition of the present invention can be any of those pigments known to be useful in coating compositions for carbonless copying paper.
- the pigments can be selected from, for example, Ansilex (Kaolin product manufactured by Engelhard), Hydral (hydrated alumina manufactured by Alcoa), M-60 (calcium carbonate - 70% dispersion in water manufactured by Mississippi Lime Co.) and Exsilon (Kaolin product manufactured by Engelhard).
- the pigment is used in an amount preferably ranging from 60 to 93 parts, more preferably from 80 to 90 parts, per 100 parts of the pigment and resin.
- the binder component of the coating composition of the present invention can be any of those binders known to be useful in coating compositions for carbonless copying paper.
- the binders can be selected from, for example, Penford Gum (PG) 290, Penford Gum (PG) 380 (both manufactured by Pennick and Ford) and latex.
- the binder is used in an amount of preferably ranging from 5 to 25 parts, more preferably from 10 to 20 parts, per 100 parts of the pigment and resin.
- compositions of the present invention can include, for example, dispersing agents, such as, Tamol 850 (anionic polymer-type dispersing agent) and Colloid 230 (dispersing agent manufactured by Colloids, Inc.); ph adjustment agents, such as, ammonia 26°Be (alkaline pH adjuster); and cross-linking agents, such as, Sunrez 700m (a starch cross-linking agent manufactured by Sun Chemicals, Inc.).
- dispersing agents such as, Tamol 850 (anionic polymer-type dispersing agent) and Colloid 230 (dispersing agent manufactured by Colloids, Inc.)
- ph adjustment agents such as, ammonia 26°Be (alkaline pH adjuster)
- cross-linking agents such as, Sunrez 700m (a starch cross-linking agent manufactured by Sun Chemicals, Inc.).
- a carbonless copying system includes a recording substrate, a first image-forming component, and a complementary image-forming component.
- the first image-forming component in accordance with the invention is a mixture of a resin dispersion which is a phenol/aldehyde condensation product formed by the interaction of an alkyl-substituted salicylic acid, an alkyl-substituted phenol, an aldehyde and a metal source; a binder; and a pigment.
- the resin may preferably be HRJ-10176 or HRJ-10802.
- the complementary image-forming component is encapsulated in microcapsules and is capable of reacting with the first image-forming component to produce a colored reaction product.
- the first image-forming component and the complementary image-forming component are arranged in juxtaposed contact with one another whereby the application of pressure in selected areas upon the carbonless system causes a colored image to form on corresponding areas of the recording substrate.
- the complementary image-forming component is preferably a colorless dye precursor encapsulated in microcapsules.
- Representative colorless dye precursors that can be utilized as the complementary image-forming component include, for example, crystal violet lactone, benzol leucomethylene blue, rhodamine lactam, the p-toluene sulfonate of Michler's hydrol, and any of the various chromogenic compounds that are capable of changing from a colorless to a colored form on contact with an acidic substance.
- the microcapsules utilized for enveloping the dye precursor material may comprise a shell or wall of polymeric material, may have generally continuous walls and may range from about 0.1 to about 500 microns in diameter.
- the complementary image-forming component is carried by a transfer substrate which is in juxtaposed contact with the recording substrate.
- the image-forming component may be adhered to the transfer substrate by utilizing a known binder.
- the recording substrate and the transfer substrate are arranged adjacent to one another so that the first image-forming component and the complementary image-forming component are in juxtaposed, i.e., pressure sensitive, contact with respect to one another.
- pressure is applied to the transfer substrate at locations corresponding to areas containing the complementary image-forming component, microcapsules of the complementary image-forming component are ruptured and the contained dye precursor is released to contact and react with the first image-forming component on the recording substrate to form a standard colored image thereon.
- both the first image-forming component and the complementary image-forming component can be applied to the recording substrate.
- a transfer substrate can be utilized wherein the complementary image-forming component is carried on the transfer substrate and a first image-forming component is carried by the recording substrate.
- the external pressure is necessary to cause the microcapsules containing the complementary image-forming component to rupture may be applied to either the recording substrate itself, or in the embodiment utilizing the transfer substrate, to the transfer substrate.
- the carbonless copying system of the invention may also contain a plurality of intermediate substrates, or CFB (coated front and back) sheets, located between the transfer substrate and the recording substrate.
- CFB substrate sheets are coated on the front side of the recording substrate with the first image-forming component (corresponding to the component on the recording substrate) and are also coated on the back side with the complementary image-forming component (corresponding to the component on the transfer substrate).
- the intermediate sheets are capable of functioning as both recording and transfer sheets by forming the colored reaction products on their front side like the recording substrate, and they also enable the transfer of the complementary image-forming components to successive sheets, like the transfer substrate. This enables the formation of multiple copies of sheets, each sheet containing the standard colored images.
- the coating compositions of the examples were applied to the recording substrate by utilizing a hand drawdown with a wire round rod. A slurry was placed on the paper and the wire round rod was pulled across the surface of the paper by hand to spread the slurry coating. After the substrate was coated, the substrate was placed in a drying oven until the coating reached ambient humidity.
- Table 1 illustrates that the enhanced speed CF coating of the present invention (HRJ-10176 resin) provides for faster imaging than the standard CF coating (HRJ-2456 resin), both at room temperature and at 32°F.
- HRJ-10176 resin the enhanced speed CF coating of the present invention
- HRJ-2456 resin the standard CF coating
- the faster imaging is more pronounced at 32°F. It can be seen that, at 32°F, it takes 5 minutes for carbonless paper utilizing the resin of the invention to form an image having a % reflectance of 59.9.
- the % reflectance is 79.1 after 5 minutes, and it takes 20 minutes to form an image having a % reflectance of 58.7.
- both HRJ-10176 and HRJ-10802 provide faster imaging than conventional HRJ-2456 at room temperature and also at 32°F.
- the faster imaging is more pronounced at 32°F.
- a production sample (55 gal drum) of HRJ-10176 was used for testing in the lab (compared to a sample of HRJ-2456 and lab sample of HRJ-10176).
- the improved results achieved by the resin of the invention may be due to the fact that the resin of the invention is a condensation product of a salicylic acid.
- Salicylic acid may act as an enhancer to assist the dye in reacting with the resin.
Landscapes
- 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 |
---|---|---|---|
US60261990A | 1990-10-24 | 1990-10-24 | |
US602619 | 1996-02-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0482409A1 true EP0482409A1 (de) | 1992-04-29 |
Family
ID=24412094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP9191117025A Withdrawn EP0482409A1 (de) | 1990-10-24 | 1991-10-07 | Kohlefreies Papier mit erhöhter Geschwindigkeit |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0482409A1 (de) |
JP (1) | JPH04263986A (de) |
AU (1) | AU8606691A (de) |
CA (1) | CA2054032A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0584969A2 (de) * | 1992-08-20 | 1994-03-02 | Moore Business Forms, Inc. | Beschichtungszusammensetzung zum Erzeugen eines kohlenstoffreien Kopierpapiers sowie damit verschichteles papier |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0268878A2 (de) * | 1986-11-05 | 1988-06-01 | MITSUI TOATSU CHEMICALS, Inc. | Salicylsäurecopolymere und die Metallsalze, Herstellungsverfahren, Farbeentwickler mit diesen Copolymer-Metallsalzen und Aufzeichnungsschichten damit |
EP0338808A2 (de) * | 1988-04-20 | 1989-10-25 | Schenectady International, Inc. | Alkylsalicylat-Harz für Kopierpapier ohne Kohlenstoff und dessen Verwendung zu Aufzeichnungszwecken |
EP0361040A2 (de) * | 1988-08-15 | 1990-04-04 | MITSUI TOATSU CHEMICALS, Inc. | Geruchlose von polyvalenten Metallen modifizierte Salizylsäurecopolymere, deren Herstellungsverfahren und ihre Verwendung als Farbentwicklungsmittel für druckempfindliche Aufzeichnungspapierschichten |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50145739A (de) * | 1974-05-15 | 1975-11-22 |
-
1991
- 1991-10-07 EP EP9191117025A patent/EP0482409A1/de not_active Withdrawn
- 1991-10-23 AU AU86066/91A patent/AU8606691A/en not_active Abandoned
- 1991-10-23 JP JP3304039A patent/JPH04263986A/ja active Pending
- 1991-10-23 CA CA 2054032 patent/CA2054032A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0268878A2 (de) * | 1986-11-05 | 1988-06-01 | MITSUI TOATSU CHEMICALS, Inc. | Salicylsäurecopolymere und die Metallsalze, Herstellungsverfahren, Farbeentwickler mit diesen Copolymer-Metallsalzen und Aufzeichnungsschichten damit |
EP0338808A2 (de) * | 1988-04-20 | 1989-10-25 | Schenectady International, Inc. | Alkylsalicylat-Harz für Kopierpapier ohne Kohlenstoff und dessen Verwendung zu Aufzeichnungszwecken |
EP0361040A2 (de) * | 1988-08-15 | 1990-04-04 | MITSUI TOATSU CHEMICALS, Inc. | Geruchlose von polyvalenten Metallen modifizierte Salizylsäurecopolymere, deren Herstellungsverfahren und ihre Verwendung als Farbentwicklungsmittel für druckempfindliche Aufzeichnungspapierschichten |
Non-Patent Citations (3)
Title |
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PATENT ABSTRACTS OF JAPAN vol. 12, no. 340 (M-740)(3187) 13 September 1988 & JP-A-63 099 983 ( MITSUI TOATSU CHEM INC ) 2 May 1988 * |
PATENT ABSTRACTS OF JAPAN vol. 13, no. 115 (C-578)(3463) 20 March 1989 & JP-A-63 289 017 ( MITSUI TOATSU CHEM INC ) 25 November 1988 * |
WORLD PATENTS INDEX LATEST Section PQ, Week 8826, Derwent Publications Ltd., London, GB; Class P75, AN 88-178& JP-A-63 115 782 (MITSUI TOATSU CHEM INC) 20 May 1988 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0584969A2 (de) * | 1992-08-20 | 1994-03-02 | Moore Business Forms, Inc. | Beschichtungszusammensetzung zum Erzeugen eines kohlenstoffreien Kopierpapiers sowie damit verschichteles papier |
EP0584969A3 (de) * | 1992-08-20 | 1995-01-25 | Moore Business Forms Inc | Beschichtungszusammensetzung zum Erzeugen eines kohlenstoffreien Kopierpapiers sowie damit verschichteles papier. |
Also Published As
Publication number | Publication date |
---|---|
AU8606691A (en) | 1992-04-30 |
JPH04263986A (ja) | 1992-09-18 |
CA2054032A1 (en) | 1992-04-25 |
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