GB2217233A - Paper coating - Google Patents

Paper coating Download PDF

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Publication number
GB2217233A
GB2217233A GB8908201A GB8908201A GB2217233A GB 2217233 A GB2217233 A GB 2217233A GB 8908201 A GB8908201 A GB 8908201A GB 8908201 A GB8908201 A GB 8908201A GB 2217233 A GB2217233 A GB 2217233A
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GB
United Kingdom
Prior art keywords
coat
paper
smectite
pigment
coats
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Withdrawn
Application number
GB8908201A
Other versions
GB8908201D0 (en
Inventor
Howard Goodman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imerys Minerals Ltd
Original Assignee
ECC International Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by ECC International Ltd filed Critical ECC International Ltd
Publication of GB8908201D0 publication Critical patent/GB8908201D0/en
Publication of GB2217233A publication Critical patent/GB2217233A/en
Withdrawn legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/80Paper comprising more than one coating
    • D21H19/82Paper comprising more than one coating superposed
    • D21H19/822Paper comprising more than one coating superposed two superposed coatings, both being pigmented
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/502Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording characterised by structural details, e.g. multilayer materials
    • B41M5/506Intermediate layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/502Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording characterised by structural details, e.g. multilayer materials
    • B41M5/508Supports
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5218Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)

Description

1 c1 A -v 1 221723,35 PAPER COATING
This invention relates to coated paper suitable for printing by the rotogravure process or by offset lithographjp and to'methoas of preparing the same. THE PRIOR ART
GB-2039789 discloses an electrostatic imaging sheet wherein one side of the sheet is electrically conductive and the other side of the sheet has a continuous dielectric layer comprising a nixture of a smectite clay and an electrically insulating polymer.
THE INVENTION According to a first aspect of the present invention there is provided a paper suitable for printing by offset lithography and/or by a rotogravure process, comprising a cellulosic sheet material provided with first and second pigmented coats each of which is hydrophilic, water absorbent and porous, said first coat being a base coat and said second coat being a top coat; wherein the pigment of one of said coats is predominantly of non smectite-type nature, whilst the pigment of the other of the said coats is predominantly of a smectite-type nature comprising at least 60% by weight of a water-swellable smectite-type clay.
According to a second aspect of the present invention there is provided a method of preparing paper suitable for printing by offset lithography and/or by a rotogravure process which method includes the steps of applying the following pigmented coats to a cellulosic sheet material; (i) a first, or base, coat; and (ii) a second, or top, coat; wherein the pigment of one of said coats-is predominantly of non smectite- type nature and the pigment of the other of said coats is predominantly of a smectite-type nature comprising at least 60% by weight of a waterswellable smectite-type clay.
L f According to a third aspect of the present invention there is provided a method of printing an image on a paper, using a rotogravure or an offset lithography printing process, the paper on which the image is printed comprising a - cellulosic sheet material provided with first and second pigmented coats each of which is hydrophilic, water absorbent -and porous, said first coat being a base coat and said second coat being a top coat; wherein the pigment of one o said coats is predominantly of non smectite-type nature, whilst the pigment of the other of the said coats is predominantly of a smectite-type nature comprising at least 60% by weight of a water-swellable smectite-type clay.
In order to be suitable for use in an offset lithographic printing process, both the base coat and the top coat of a paper according to the present invention need to be hydrophilic, water absorbent and porous so that water can be transported rapidly away from the surface of the paper.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The smectite-type clay may, for example, be bentonite, montmorillonite, hectorite, saponite or fullers earth, but especially preferred is a natural bentonite which has, or has been treated to have, predominantly sodium ions in its exchangeable.cation sites. Preferably, the pigment which is predominantly of a smectite-type nature contain at least 75%, more preferably at least 90%, by weight of the smectite-type qlay.
The pigment employed in the other coating may, for example, be a white pigment, other than a smectite-type clay, such as a kaolin clay, a natural or a synthetic calcium carbonate, talc or a natural or synthetic calcium sulphate. Alternatively, other conventional pigments may be employed. It is possible that the pigment in the other coating may, in some instances, 4 4 also contain a minor amount of a smectite-type clay.
The paper may be provided with further coatings. It is preferred however, that the material comprises two coatings,'the top coating including a pigment which is predominantly smectite-type clay, typically bentonite, whilst the other coating, or base coating, includes a pigment which is substantially non-smectite in nature. It is, however, within the scope of the invention to provide a paper in which the'pigment of the base coating is predominantly smectite clay in nature and the top coating substantially non-smectite clay. Most preferably, the base coating contains kaolin and the top coating bentonite.
Each of the coatings is preferably bound together by an adhesive which may, for instance, be one of the conventional adhesives used in paper coating, such as a rubber latex, for example an acrylic copolymer latex (styrene butadiene rubber latex), or a starch. When the pigment is not a smectite-type clay, the quantity of adhesive solids required is in the range of from 1 to 20 parts by weight to 100 parts by weight of the pigment. When the pigment is predominantly of a smectite type nafure, the quantity of adhesive solids may be up to 300 parts by weight to 100 parts by weight of the pigment; in some circumstances, if the smectitetype coat is the base coat, the pigment may be employed in the absence of an adhesive as it has been found that adequate adhesion of the clay to the cellulosic fibres is achieved without the presence of an adhesive. When an adhesive is used it is found that for a paper intended for rotogravure printing a latex adhesive is preferred and especially an acrylic copolymer latex. Generally the quantity of adhesive used will be in the range from 1 to 300 parts by weight of dry polymer to 100 parts by weight of dry smectite clay.
Preferably, the pigment of the coat which is predominantly smectite-type in nature is provided by applying to the sheet material an aqueous suspension comprising up to 20% by weight of a pigment comprising at least 60% by weight of a water-swellable smectite 5 clay. DETAILED DESCRIPTION
The invention is further illustrated by the following Examples.
EXAMPLE 1
A rotogravure base paper of substance weight 38 gm-2 (grams per square metre) was coated by means of a laboratory coating apparatus of the type described in British Patent Specification No. 1032536 running at a speed-of 200m min-l. Three different coating procedures were used, namely:A single coat of a composition consisting of 100 parts by weight of a kaolin clay, 5 parts by weight of an acrylic copolymer latex adhesive (dry basis), and water to form a suspension containing 57.4% by weight of total solids. The kaolin clay had a particle size distribution such that 6% by weight consisted of particles having an equivalent spherical diameter larger than 10 microns and 43% by weight consisted of particles having an equivalent spherical diameter smaller than 2 microns. The latex contained 50% weight of acrylic copolymer solids. Samples of the base paper were coated with the composition at four different coat weights.
2. a). A base coat of an aqueous suspension containing 5% by weight of the European bentonite.having sodium and calcium exchangeable cations. The coat weight of bentonite applied to the base paper was 0.5 gm-2. b). A top coat of the same composition as was described under 1 above applied at four different coat weights.
3. a). A base coat of the same composition as was described under 1 above applied at four different coat weights.
b). A top coat of the same aqueous suspension of bentonite as was described under 2a. above at a coat weight of 0.5 gm-2.
Samples of the hand-coated sheets were printed with test rotogravure prints on a Winston-e proof press using the technique described in the article "Realistic paper tests for various printing processes" by A. Swan, published in "Printing Technology". Vol 13, No. 1, April 1969, pages 9-22. A gravure, printing cylinder was used with an area of deeply etched cells to give a solid black area and an area of less deeply etched cells to give a half tone area. The gloss of the solid black areas on the tests prints was measured by the Tappi Standard Method No. T480 ts-65 and the print density of the solid black areas was determined according to the formula:Print density = ogjo (1/reflectance) Where the reflectance is the fraction of the incident light of wavelength 574 nm reflected back from the black area.
A further measurement of print density was performed on the reverse side of the paper in the region of the solid black area in order to determine the degree of "strike through" of the printing ink.
In addition, the degree of "speckle" in the half tone area of each print was determined by estimating the percentage of gravure printing dots which were missing from the test print. In addition the gloss of an un-printed area of each coated paper sample was also measured by the TAPPI Standard Method No. T480ts-65. The results obtained are set forth in Table I below:- W W M, 0 0 (v F M-f LM Ln 0 n 0 TABLE 1
Coating Coat weight Close of Gloss of Print density A missing procedure of kaolin unprinted solid solid reverse dote (half comppition paper black black of solid tone area) (9m-) area area area 1 2.2 34 51 1.74 0.26 4.6 1 3.6 42 55 1.76 0.26 3.4 1 5.7 49 48 1.64 0.25 2.4 1 7.2 52 50 1.67 0.22 1.2 2 1.6 32 64 1.95 0.24 4.7 2 2.7 34 65 1.94 0.24 5.1 2 5.7 41 60 1.82 0.24 2.5 2 8.1 46 54 1.70 0.24 1.9 3 2.7 36 65 1.98 0.22 5.1 3 4.1 43 73 2.06 0.21. 3.3 3 6.2 48 75 2.11 0.20 2.4 3 7.7 50 73 2.08 0.19 1.0 01 %I, 1 1 a 1 a 11 These results show that the application of a coating of 0.5 gm-2 of bentonite to the base paper as one coat in a two-coat procedure effects an increase in the gloss,and print density of the solid black printed area. When the bentonite is applied as a base coat the increase is relatively small but when the bentonite suspension is applied as a top coat over a coating containing kaolin the increase in both gloss and print density is surprisingly large even thougIr the gloss of the un-printed area is substantially unaffected by the presence of the bentonite. The half-tone print qualities, as indicated by the percentage of missing dots, are also substantially unaffected by the presence of the bentonite coating.
EXAMPLE 2
An offset base paper of substance weight 65 gm-2 was coated by means of the laboratory coating apparatus used in Example 1 running at a speed of 400 m min-1 firstly with a composition consisting of:
100 parts by weight of a kaolin clay 11 parts by weight of styrene butadiene rubber latex (dry basis) 1 part by weight of sodium carboxymethyl cellulose; -water to form a suspension containing 60.8% by weight of total solids The kaolin clay had a particle size distribution such that 0.2% by weight consisted of particles having an equivalent spherical diameter larger than 10 microns and 10% by weight consisted of particles having an equivalent spherical diameter smaller than 2 microns. The latex contained 50% by weight of styrene butadiene rubber solids. Samples of the base paper were coated with this composition at four different coat weights.
Samples of the paper coated with the composition described above at four different coat weight were each treated with a second coating composition which consisted of a 5% by weight suspension in water of a European bentonite having sodium and calcium exchangeable cations at a coat weight of 0.5 gm- 2.
SampIes.of the coated paper were tested for offset lithography printing properties by means of an IGT Model AC2 printability tester. The paper samples were clipped to the moving sector of the instrument which was set to move at a constant velocity- of 1 ms-1. An aluminium alloy damping roll of face width 25 mm and a rubber covered printing roll of face width 20 mm were rotatably and removabiy mounted on spindles provided on the fixed part of the instrument with the damping roll contacting the surface of the paper sample 70 mm in advance of the line of contact of the printing roll with the paper surface in the sense of the direction of relative motion between the sector bearing the paper sample and the rolls. As a result of this configuration each paper sample was printed with a strip of solid colour 20 mm in width, the first 70 mm 20" being printed on dry paper and the remaining 140 mm on pre-wetted paper. During operation the damping roll was biased against the paper sample with a force of 25 kg and the printing roll was biased against the sample with a force of 50 kg. Both the damping roll and the printing roll had an overall diameter of 68 mm.
Before each test the damping roll was loaded with a substantially identical weight of water. namely approximately 0.6 g of water per square metre of roll surface area by condensation of water vapour on the surface of the roll. The damping roll was-placed in a refrigerator having an internal temperature of -8 + 10C and a coiled temperature probe connected to a digital thermometer was placed in the central spindle hole of the roll. When the temperature recorded by the thermometer had fallen to +50C the roll was transferred to a desiccator in which a humidity of 55% RH was A maintained by means of a saturated solution of sodium dichromate. When the temperature of the atmosphere in the thermometer had fallen to +50C the roll was transferred to a desiccator in which a humidity of 55% 5 RH was maintained by means of a saturated solution of.sodium dichromate. The temperature of the atmosphere in the laboratory was controlled at 20 + 10C. The roll was left in the desiccator for a time of 1 minute 55 seconds and the printability test was performed after another 5 seconds using a printing roll which had been pre-inked with Ault & Wiborg 4-Colour Process Gloss Magenta offset lithography ink.
The block of solid colour printed on the dry and pre-wetted areas, respectively, of the paper samples was tested for print gloss by means of a Hunterlab Glossmeter Model D16 and at an angle of 750 with the normal to the paper surface in accordance with TAPPI Standard No. T480ts-65, the mean of five determinations for each area being recorded. 20 The block of solid colour printed on the dry and pre-wetted areas, respectively, was also tested for print density by means of a Macbeth RD514 Reflection Densitometer, in- this case the mean of ten determinations for each area being recorded. In addition the gloss of an un-printed area of each coated paper sample was also measured by the TAPPI Standard Method No. T480ts-65. The results obtained are set forth in Table II below:- 1 w w Ni M >-a -j (A Ln 0 ui 0 Ln 0 TABLE 11
Coat weight Coat weight Gloss of Gloss of solid Print density of kaolin of bentonite unprinted colour area composition composition paper (9m-2) (9m-2) Dry Wet Dry Wet 2.7 0 7 15 15 1.03 1.04 4.3 0 9 23 21 1.08 1.07 6.2 0 12 30 29 1.14 1.14 8.1 0 13 33 33 1.12 1.13 2.7 o.5 0 20 16 1.04 0.94 4.3 0.5 11 39 23 1.12 0.92 6.2 0.5 14 39 34 1.17 1.00 8.1 0.5 14 38 33 1.15 0.94 0 1 -A 0 i 1 These results show that although the gloss of the un-printed paper for a given coat weight remains substantially the same. there is a significant increase in the gloss of the block of colour printed on the dry area. The print density remains almost unchanged when a top coat of the bentonite composition is applied except for a small decrease in the print density on the pre-wetted area.
EXAMPLE 3
A matt offset printing base paper of substance weight 59 gm-2 was coated in two stages, each stage being by means of the laboratory coating apparatus used in Examples 1 and 2 running at a speed of 4000 m min-1. In the first stage the coating composition used consisted of: 100 parts by weight of natural calcium carbonate 11 parts by weight of a styrene butadiene rubber latex (dry basis) 0.5 parts by weight of sodium carboxymethyl cellulose 0.1 part by weight of sodium hydroxide water to form a uspension containing 66.9% by weight of total solids. The natural calcium carbonate was a ground marble having a particle size distribution such that 1% by weight consisted of particles having an equivalent spherical diameter larger than 10 microns and-90% by weight consisting of particles having an equivalent spherical diameter small than 2 microns. The latex contained 50% by weight of styrene butadiene rubber solids ' In the second stage, samples of the paper coated with the above calcium carbonate containing composition were tested with three different suspensions in water of the same bentonite as was used in Examples 1 and 2. The three suspensions contained respectively 4%, 8% and 12% by weight of bentonite, but in each case the coat weight of bentonite actually applied to the paper was about 5 gm-2.
The same offset lithography printing tests as are described in Example 2 were performed on the paper samples coated in two stages and, as a comparison, on a sample coated only with the calcium carbonate containing composition. In addition the gloss of an un-printed area of each coated paper sample was also 10 measured by the TAPPI Standard Method No. T480ts65.
The results obtained are set forth in Table III below:- z k LAJ Ni m -4 F Lm 0 Lri 0 Ul CD by weight 00 of bentonite in suspension paper TABLE III
Gloss of Gloss of solid unprinted colour area dry wet Print density dry wet 0 23 44 46 1.28 1.30 4 27 51 51 1.29 1.26 8 28 57 56 1.32 1.29 12 28 57 54 1.36 1.30 8 f 9 1 -1 W 1 14- These results show the gloss of the solid colour printed area increases to a greater extent than the gloss of the un-printed paper. both on the dry and on the pre-wetted areas of paper, as the proportion by weight of bentonite in the second coating composition increases. The print density of the solid colour area printed on dry paper also increases although the print density of the solid colour printed on-pre- wetted paper remains substantially unchanged.
i

Claims (15)

1. A paper, suitable for printing, comprising a cellulosic sheet material provided with first and second pigmented coats each of which is hydrophilic, water absorbent and porous. said first coat being a base coat and said second coat being a top coat; wherein the pigment of one of said coats is predominantly of non smectite-type nature, whilst the pigment of the other of the said coats is-predominantly of a smectite-type nature comprising at least 60% by weight of.a water- swellable smectite-type clay._
2. A paper as claimed in claim 1, wherein the coat comprising predominantly a smectite-type clay as the pigment is the top coat.
3. A paper as claimed in claim 1, wherein the coat comprising predominantly a smectite-type clay as the pigment is-the base coat.
4. A paper as claimed in claim 1. 2 or 3, wherein said first and second coats are the only coats provided on the sheet material.
5. A paper as claimed in claim 1, 2 or 3, wherein the sheet material is provided with one or more further coats between said base and top coats.
6. A paper as claimed in any preceding claim, wherein the coat weight of the smectite-type clay coat is no greater than 5 g.m-2.
7. A paper as claimed in any preceding claim.
wherein one or both of the base and top coats also includes an adhesive.
8. A paper as claimed in any preceding claim, wherein the pigment of said other of the coats comprises at least 75% by weight of the smectite-type clay.
9. A paper as claimed in claim 8, wherein the pigment of said other of the coats comprises at least 90% by weight of the smectite-type clay.
D applying to the sheet material an aqueous suspension comprising up to 20% by weight of a pigment comprising at least 60% by weight of a waterswellable smectite clay.
16. A method according to claim 15, wherein the aqueous suspension domprises no greater than 15% by weight of the pigment comprising smectite-type clay.
17. A method of printing an image on a paper, using a rotogravure or an offset lithography printing process, the paper on which the image is printed comprising a cellulosic sheet material provided with first and second pigmented coats each of which is hydrophilic, water absorbent and porous, said first coat being a base coat and said second coat being a top coat; wherein the pigment of one of said coats is predominantly of non smectite-type nature, whilst the pigment of the other of the said coats is predominantly of a smectite-type nature comprising at least 60% by weight of a water-swellable smectite-type clay.
18. A paper substantially as hereinbefore described, with reference to the accompanying Examples.
19. A method of preparing a paper substantially as hereinbefore described, with reference to the accompanying drawings.
1W9 atThe nt 0Moe. B House, M71 Holborla, London WC1R 4TP. Purther 00ples m&ybe obtLndtmmnle ptor&m.
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10. A paper as claimed in Claim 2, or any of Claims 3 to 9 when appendant to Claim 2, wherein the pigment of said base coat is predominantly a white pigment other than a smectite-type clay.
11. A paper,, suitable for printing, compr ising a cellulosic sheet material provided with first and second coats each of which is generally hydrophilic in nature and comprises at least 70% by weight pigment, said first coat being a base coat and said second coat being a top coat, wherein the pigment of the base coat is predominantly of a non-smectite nature and the pigment of the top coat comprises at least 60% by weight of a water-swellable smectite-type clay and forms a coating having a coat weight no greater than 5 g.m-2.
12. A paper as claimed in claim 11, wherein the major pigment in the base coat is a white pigment other than a smectite-type clay.
13. A paper as claimed in Claim 12, wherein the major pigment in the base layer is a kaolin clay, a natural or synthetic calcium carbonate, talc or a natural or synthetic calcium sulphate.
14. A method of preparing paper suitable for printing which method includes the steps of applying the following pigmented coats to a cellulosic sheet material; (i) a first, or base, coat; and (ii) a second, or top, coat; wherein the pigment of one of said coats is predominantly of non-smectite-type nature and the pigment of the other of said coats is predominantly of a smectite-type nature comprising at least 60% by weight of a water-swellable smectite-type clay.
15. A method of preparing paper as claimed in claim 14,, wherein the pigment of the coat which is predominantly smectite-type in nature is provided by 1
GB8908201A 1988-04-12 1989-04-12 Paper coating Withdrawn GB2217233A (en)

Applications Claiming Priority (1)

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GB888808552A GB8808552D0 (en) 1988-04-12 1988-04-12 Paper coating

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GB8908201D0 GB8908201D0 (en) 1989-05-24
GB2217233A true GB2217233A (en) 1989-10-25

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GB888808552A Pending GB8808552D0 (en) 1988-04-12 1988-04-12 Paper coating
GB8908201A Withdrawn GB2217233A (en) 1988-04-12 1989-04-12 Paper coating

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GB888808552A Pending GB8808552D0 (en) 1988-04-12 1988-04-12 Paper coating

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EP (1) EP0337771A1 (en)
JP (1) JPH02503933A (en)
BR (1) BR8906809A (en)
FI (1) FI895929A0 (en)
GB (2) GB8808552D0 (en)
WO (1) WO1989009852A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2299036A (en) * 1995-03-22 1996-09-25 Coated Papers Limited Coated Paper

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4438306A1 (en) * 1994-10-26 1996-05-02 Sued Chemie Ag Pigments for print media using the inkjet printing process
DE19527161A1 (en) * 1995-07-25 1997-01-30 Sued Chemie Ag Pigment mixture and coating color with improved gravure suitability
FR2768161B1 (en) * 1997-09-10 1999-10-15 Ahlstrom Paper Group Research IMPROVED PRINTABLE PAPER OR CARDBOARD, MANUFACTURING METHOD AND USE
SE538111C2 (en) * 2013-10-09 2016-03-08 Stora Enso Oyj Process for manufacturing a web-shaped composite as well as a single composite made by the method
EP3156540A1 (en) 2015-10-12 2017-04-19 Omya International AG Process for the deinking of coated paper or paperboard

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE736450C (en) * 1940-08-01 1943-06-17 Johannes Bauer Dipl Ing Process for the production of coated papers
US2371266A (en) * 1942-06-26 1945-03-13 Reconstruction Finance Corp Surface sized paper product
US3508952A (en) * 1967-06-28 1970-04-28 Grace W R & Co Coated paper article and process therefor
GB1363563A (en) * 1972-01-21 1974-08-14 Scm Corp Electroconductive paper
GB2039789B (en) * 1978-11-13 1983-04-13 Fellows A Electrostatic imaging sheet
DE3506278A1 (en) * 1985-02-22 1986-08-28 Inst Zellstoff & Papier METHOD FOR IMPROVING THE HOLDOUT OF PRINT INKS, VARNISHES AND COATING MEASURES ON FABRIC MATERIALS OF FIBERS, AND MEASURES FOR IMPLEMENTING THE METHOD AND AREA PRODUCED BY IT

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2299036A (en) * 1995-03-22 1996-09-25 Coated Papers Limited Coated Paper

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BR8906809A (en) 1990-12-04
GB8908201D0 (en) 1989-05-24
JPH02503933A (en) 1990-11-15
WO1989009852A1 (en) 1989-10-19
EP0337771A1 (en) 1989-10-18
GB8808552D0 (en) 1988-05-11
FI895929A0 (en) 1989-12-12

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