Printable paper; process for producing printable paper; and use thereof

Information

  • Patent Grant
  • 8357447
  • Patent Number
    8,357,447
  • Date Filed
    Thursday, March 12, 2009
    15 years ago
  • Date Issued
    Tuesday, January 22, 2013
    12 years ago
Abstract
A printable paper comprising a water-resistant support having two optionally subbed sides and a single layer on at least one of said optionally subbed sides, wherein said single layer has no substantial compositional variation, has a layer thickness of at least 3 μm, a pore volume of at least 1.2 mL/m2 and comprises at least one porous pigment; a process for producing a printable paper comprising the steps of: (i) optionally providing a water-resistant support having two sides with a subbing layer on at least one side; (ii) providing at least one side of said optionally subbed water-resistant support with a single layer having no substantial compositional variation, said single layer being applied to said optionally subbed water-resistant support as at least one wet aqueous layer in a single pass for each side of said water-resistant support, said at least one aqueous layer comprising at least one latex, at least one pigment, at least one binder and optionally at least one insolubilizing agent, wherein said latex is an anionic acrylic latex or an aliphatic polyurethane latex; and the use in printing of the above-described printable paper or that obtained by the above-described production process.
Description
FIELD OF THE INVENTION

The present invention concerns a printable paper, a process for producing printable paper, and the use thereof in offset printing.


BACKGROUND OF THE INVENTION

Synthetic papers may be classified into two different types: one with a fibrous structure like cellulose paper, with synthetic fibers made from polyamides, polyester, or polyolefins replacing the cellulose fibers; and one in which a film is directly extruded from a thermoplastic polymer. These products differ considerably in their structure from cellulose paper and thus present a variety of different problems.


Extruded film is produced either by the cast film process or the blown film process in which the melt is forced through a circular die. A variant of the blown film process is the extrusion of foamed film in which through the addition of blowing agents (usually low boiling hydrocarbons) it is possible to produce foamed film from a variety of polymers. Two methods are used for the biaxial stretching of cast film: the simultaneous stretching process, in which the stretching is carried out in both directions at the same time, and the two-stage process, in which the two stretching operations are carried out consecutively.


Extruded films have a smooth surface which depends more on the state of the chill rolls than on the material itself. There are no cavities with capillary activity such as between the fibers of cellulose paper or synthetic fiber webs. This combination of smooth surface, low absorbing power, and non-polar structure frequently makes it difficult to print on polymer films: drying times are long, and the adhesion of the printing ink is poor.


Lunk and Stange in 1971 in Angewandte Chemie International Edition, volume 10, pages 287-294 stated that one type of surface treatment to improve the printability of extruded films is the application of a pigment coating. In the paper industry, the improvement of the surface of cellulose paper with a pigment coating had been known for some time. Typical binders for these coatings were casein, polyacrylates, or copolymers of butadiene and styrene. China clay, barium sulfate, chalk, or titanium dioxide were used as pigments. In spite of their closed, smooth surface coated papers were sufficiently absorptive for letterpress and offset printing because of their high content of mineral filler. Coated polymer films had similar properties; they could also be used for all printing processes, and the print quality was equal to that of coated papers. However, the demands of the printing industry have increased since 1971 requiring papers with ever higher printability.


GB 2 177 413A discloses a coating composition for a plastics substrate and comprising an aqueous system containing polymeric binder, pigment and antistatic agent characterised in that the binder contains carboxyl groups, that the binder:pigment dry weight ratio is in the range 15:100 to 50:100, preferably 22:100 to 35:100, the antistatic agent comprises a water soluble ionic compound present in an amount corresponding to a dry weight:pigment ratio of from 0.4:100 to 2.5:100 and in that the composition also contains an insolubilizing agent which is capable of reacting with carboxyl groups of the binder on drying the composition to insolubilize (as hereinbefore defined) the binder.


U.S. Pat. No. 5,397,637 discloses a thermoplastic resin film with satisfactory printability having a coated layer comprising a quaternary ammonium salt copolymer comprising (a) a structural unit represented by formula (I):




embedded image



wherein A represents —O— or —NH—; R1 represents a hydrogen atom or a methyl group; R2 represents an alkylene group having from 2 to 4 carbon atoms or —CH2CH(OH)—CH2—; R3, R4, R5, and R6, which may be the same or different, each represents an alkyl group having from 1 to 3 carbon atoms; R7 represents an alkyl group having from 1 to 10 carbon atoms or an aralkyl group having from 7 to 10 carbon atoms; n represents an integer of from 1 to 3; and X represents a chlorine atom, a bromine atom or an iodine atom, (b) a structural unit represented by formula (II):




embedded image



wherein R8 represents a hydrogen atom or a methyl group; and R9 represents an alkyl group having from 1 to 22 carbon atoms, an aralkyl group having from 7 to 22 carbon atoms or a cycloalkyl group having from 5 to 22 carbon atoms, and (c) a structural unit derived from a monomer copolymerizable with monomers providing structural units (a) and (b) at a (a):(b):(c) weight ratio of 30 to 70:30 to 70:0 to 40.


JP 11-107194 discloses an offset-printable synthetic paper characterized by providing at least one side of a synthetic substrate with 1-7 g/m2 of a coating layer comprising 20 to 50 wt % of polyvinyl alcohol, 20 to 50 wt % of a polyurethane resin and 20 to 50 wt % of a silica pigment, with it being preferred that the polyurethane resin is a carboxyl-containing crosslinkable polyurethane resins or a polyester-based polyurethane resin and the particle size of the silica pigment is 2-5 μm, and the synthetic paper has 20-50% opacity determined in accordance with the JIS P 8138.


U.S. Pat. No. 6,300,393 discloses a paper coating composition comprising (a) at least one binder containing a plurality of functional groups capable of reacting with carboxylic acid anhydride moieties to form chemical bonds, and (b) at least one insolubilizing agent chosen from the group consisting of compounds containing a plurality of carboxylic acid anhydride moieties per molecukar entity.


WO 03/033577A discloses a printable, opaque coated sheet, suitable for use in contact and/or association with foodstuffs, the coating comprising by dry weight of the coat: (a) from about 30% to about 70% of a copolymer of an ethylenically unsaturated acid; (b) from about 30% to about 70% of an inert particulate filler; where the coating is substantially free from any reactive binder and/or cross-linking agent. WO 03/033577A further discloses that the ethylenically unsaturated acid is preferably neutralised by ammonia and not metal cations, since this has the advantage that on drying ammonia evaporates and acid groups become less moisture sensitive compared to metal cation stabilised ethylene acrylic acid (EAA) copolymer dispersions.


US 2004/0146699A1 discloses a composite plastics sheet which is printable on at least one surface, and comprises a base layer and optionally a printable layer forming the printable surface, characterized in that the base layer has a density of 0.65 g/mL or less, or, if there is no separate adhesive layer on the surface opposite the printable surface, a density of 0.7 g/mL or less.


US 2006/0257593A1 discloses a printing sheet comprising a substrate and, on at least one side of the substrate, an image receptive coating layer with a cumulative porosity volume of pore widths below 200 nm as measured using nitrogen intrusion methods of more than 0.006 cm3 per gram paper.


EP 1 743 976A1 discloses a coated printing sheet for sheet-fed offset printing with an image receptive coating layer on a paper substrate, characterized in that the image receptive coating layer comprises a top layer and/or at least one second layer below said top layer, said top and/or second layer comprising: a pigment part, wherein this pigment part is composed of 0 to 99 parts in dry weight of a fine particulate carbonate and/or of a fine particulate kaolin 1 to 100 parts in dry weight of a fine particulate silica and a binder part, wherein this binder part is composed of: 5-20 parts in dry weight of binder and less than 4 parts in dry weight of additives.


As the foregoing present certain disadvantages, a need exists for an improved paper for use in printing processes.


SUMMARY OF THE INVENTION

In one aspect the present invention provides a printable paper comprising a water-resistant support having two optionally subbed sides and a single layer on at least one of said optionally subbed sides, wherein said single layer has no substantial compositional variation, has a layer thickness of at least 3 μm, a pore volume of at least 1.2 mL/m2 and comprises at least one porous pigment.


A further aspect of the invention provides a process for producing a printable paper comprising the steps of: (i) optionally providing a water-resistant support having two sides with a subbing layer on at least one side; and (ii) providing at least one side of said optionally subbed water-resistant support with a single layer having no substantial compositional variation, said single layer being applied to said optionally subbed water-resistant support as at least one wet aqueous layer in a single pass for each side of said water-resistant support, said at least one aqueous layer comprising at least one latex, at least one pigment, at least one binder and optionally at least one insolubilizing agent, wherein said latex is an anionic acrylic latex or an aliphatic polyurethane latex.


Another aspect of the present invention contemplates the use in printing of the above-described printable paper or that obtained by the above-described production process.


Further aspects and advantages of the invention will become apparent from the detailed description of the invention.







DETAILED DESCRIPTION OF THE INVENTION
Definitions

The term “printable paper”, as used in disclosing the present invention, means paper or a paper-like material capable of being printed by at least one conventional contact or contactless printing technique e.g. offset printing, gravure printing, screen printing, flexographic printing, electrophotographic printing and ink-jet printing.


The term “overprintable”, as used in disclosing the present invention, means capable of being overprinted by conventional impact and/or non-impact printing processes.


The term “conventional printing processes”, as used in disclosing the present invention, includes but is not restricted to ink-jet printing, intaglio printing, screen printing, flexographic printing, offset printing, stamp printing, gravure printing, dye transfer printing, thermal sublimation printing and thermal and laser-induced processes.


The term “support”, as used in disclosing the present invention, means a “self-supporting material” so as to distinguish it from a “layer” which may be coated as a solution or dispersion, evaporated or sputtered on a support, but which itself is not self-supporting. It also includes an optional conductive surface layer and any treatment necessary for, or layer applied to aid, adhesion.


The term “subbing layer”, as used in disclosing the present invention, means any layer or layer configuration required to realize adhesion between the support and the single layer, but plays no role in the printing performance of the printable paper.


The term “water-resistant support”, as used in disclosing the present invention, means a support the surfaces of which are resistant to water e.g. synthetic paper and resin-coated cellulosic paper.


The term “layer”, as used in disclosing the present invention, means a (continuous) coating covering the whole area of the entity referred to e.g. a support.


The term “single layer”, as used in disclosing the present invention, means there is only one layer on each side of the water-resistant support, although it may be applied as a plurality of wet layers in a single pass. The “single layer” has receiving properties, since otherwise the “printable paper” would not be printable.


The term “no substantial compositional variation”, as used in disclosing the present invention, means that although the layer may be coated as a plurality of wet layers the layer resulting therefrom has a compositional variation of no more than 5% by weight.


The term “porous pigment”, as used in disclosing the present invention, embraces both pigments having primary particles having an internal porosity e.g. a silica gel particles and pigments whose primary particles have no internal porosity and have a specific surface area of at least 100 m2/g, which are present as secondary particles having an internal porosity as a result of the aggregation of the primary particles e.g. flame pyrolyzed inorganic particles such as the particles in the Aerosil® range produced by Degussa.


The term “latex”, as used in disclosing the present invention, means that the latex polymer is substantially insoluble in water i.e. having a solubility in water of less than 10 mg per 100 g water at a temperature of 25° C., is prepared by standard latex preparation techniques and is supplied and used as an aqueous dispersion.


The term “water-soluble binder”, as used in disclosing the present invention, means a binder with a solubility in water of at least 1 g per 100 g water at a temperature of 25° C.


The term “inorganic opacifying pigment”, as used in disclosing the present application, means a pigment capable of opacifying (i.e. rendering more opaque) which includes substantially white inorganic pigments having a refractive index of at least 1.4 and pigments, which as a dispersion in a polymer are capable upon stretching of causing opacity due to microvoiding.


The term “whitening agent”, as used in disclosing the present invention, means a white/colourless organic compound which exhibits a blue luminescence under the influence of ambient UV-light. The term “insolubilizing agent”, as used in disclosing the present invention, means an agent capable of insolubilizing the latex.


The term “colorant”, as used in disclosing the present invention, means dyes and pigments.


The term “dye”, as used in disclosing the present invention, means a colorant having a solubility of 10 mg/L or more in the medium in which it is applied and under the ambient conditions pertaining.


The term “pigment” is defined in DIN 55943, herein incorporated by reference, as an inorganic or organic, chromatic or achromatic colouring agent that is practically insoluble in the dispersion medium under the pertaining ambient conditions, hence having a solubility of less than 10 mg/L therein.


The term “synthetic paper”, as used in disclosing the present invention, means a paper-like material produced either by forming a web from synthetic fibres or by extruding a film from thermoplastic polymers optionally coated on one or both sides with a receiving layer.


The term “film”, as used in disclosing the present invention, is an extruded sheet of a particular composition or a sheet consisting of a multiplicity of films with the same or different compositions produced by co-extrusion of liquids with the same or different compositions in contact with one another. The terms film and foil are used interchangeably in the present disclosure. The term linear polyester, as used in disclosing the present invention, means a polyester comprising hydrocarbon dimethylene and dicarboxylate monomer units.


The term “non-transparent film”, as used in disclosing the present invention, means a film capable of providing sufficient contrast to a transparent image to make the image clearly perceptible. A non-transparent film can be an “opaque film”, but need not necessarily be completely opaque in that there is no residual translucence i.e. no light penetration through the film. Optical density in transmission as measured with a MacBeth TR924 densitometer through a visible filter can provide a measure of the non-transparency of a film. ISO 2471 concerns the opacity of paper backing and is applicable when that property of a paper is involved that governs the extent to which one sheet visually obscures printed matter on underlying sheets of similar paper and defines opacity as “the ratio, expressed as a percentage, of the luminous reflectance factor of a single sheet of the paper with a black backing to the intrinsic luminous reflectance factor of the same sample with a white reflecting backing. 80 g/m2 copy paper, for example, is white, non-transparent and has an optical density of 0.5 as measured with a MacBeth TR924 densitometer through a yellow filter according to ISO 5-2 and metallized films typically have an optical density ranging from 2.0 to 3.0.


The term “voids or microvoids”, as used in disclosing the present invention, means microcells, minute closed cells, cavities, bubbles or pores or cellulation, which, for example, can be formed in an oriented polymeric film during stretching as the result of a void-initiating particle initiated by particles that are immiscible with the polyester matrix. The voids or microvoids can be unfilled or filled with air or a vapour of some sort. Even if initially unfilled the voids or microvoids may over time become filled with air or a vapour of some sort.


The term “foam”, as used in disclosing the present invention, means a substance that is formed by trapping many gas bubbles in a liquid or solid.


The term “apparent density”, as used in disclosing the present invention, means the weight of a 100 mm×100 mm piece of film with a thickness measured in contact with an inductive probe with ball tip 3 mm in diameter divided by its volume. This value assumes that the surfaces of the piece of film are flat and parallel to one another. This value corresponds to the apparent density values reported in EP-A 0 496 323 and WO 2005/105903A.


Printable Paper

Aspects of the present invention are realized by a printable paper comprising a water-resistant support having two optionally subbed sides and a single layer on at least one of said optionally subbed sides, wherein said single layer has no substantial compositional variation, has a layer thickness of at least 3 μm, a pore volume of at least 1.2 mL/m2 and comprises at least one porous pigment, with a pore volume of at least 1.5 mL/m2 being preferred.


The printing paper, according to the present invention, may be coated on both sides each with a single layer in a single pass. However, if coated on one side the non-coated side may be provided with an adhesive layer for label applications.


Porosity can be determined by standard techniques such as nitrogen porosimetry, in which nitrogen is condensed in the pores and calculating the pore volumes from the quantities of gas required to fill the pores, and mercury porosimetry, in which liquid mercury is forced into pores by increasing the external pressure, the amount of mercury required to fill the pores being increased incrementally.


According to a first embodiment of the printable paper, according to the present invention, the printable paper is exclusive of an antistatic agent comprising a water-soluble ionic inorganic compound.


According to a second embodiment of the printable paper, according to the present invention, the opacity of said printable paper determined according to ASTM D589 C/2° is greater than 90%.


According to a third embodiment of the printable paper, according to the present invention, the single layer further comprises a hardened melamine-formaldehyde resin e.g. by hardening Madurit MW15 from Vianova Resins N.V.


According to a fourth embodiment of the present invention, the single layer further contains a hardened proteinaceous substance e.g. by the hardening of the ammonium salt of casein.


Water-Resistant Support

According to a fifth embodiment of the printable paper, according to the present invention, said water-resistant support is provided with a subbing layer on at least one side thereof.


The term “water-resistant support”, as used in disclosing the present invention, means a support the surfaces of which are resistant to water. Such supports enable overcoating with aqueous solutions or dispersions without affecting the “water-resistant support”.


Water-resistant supports include resin-coated cellulosic paper, webs having a fibrous structure formed with synthetic fibers and webs in which a film is directly extruded from a thermoplastic polymer. The resin-coating of resin-coated cellulosic paper can be rendered non-transparent by the inclusion of opacifying pigments therein. Webs having a fibrous structure formed with synthetic fibers and webs in which a film is directly extruded from a thermoplastic polymer can be rendered non-transparent by the inclusion of opacifying pigments. Furthermore, webs in which a film is directly extruded from a thermoplastic polymer can be also rendered non-transparent by axial stretching-induced microvoid formation resulting from the presence of poorly compatible dispersions of amorphous high polymers with a higher glass transition temperature than the glass transition temperature or melting point of the matrix polymer and/or the crystalline high polymers which melt at a higher temperature than the glass transition temperature or melting point of the matrix polymer and axially stretching the extruded film. Widely used matrix polymers include polyethylene, polypropylene, polystyrene, polyamide and polyester.


According to a sixth embodiment of the printable paper, according to the present invention, said water-resistant support is resin-coated cellulosic paper, a web having a fibrous structure formed with synthetic fibers or a web in which a film is directly extruded from a thermoplastic polymer.


According to a seventh embodiment of the printable paper, according to the present invention, said water-resistant support comprises at least 50% by weight of a linear polyester.


According to an eighth embodiment of the printable paper, according to the present invention, said water-resistant support comprises at least 50% by weight of a linear polyester and an opacifying pigment, the opacifying pigment being preferably selected from the group consisting of silica, zinc oxide, zinc sulphide, lithopone, barium sulphate, calcium carbonate, titanium dioxide, aluminium phosphate and clays.


According to a ninth embodiment of the printable paper, according to the present invention, said water-resistant support is a non-transparent microvoided axially stretched directly extruded thermoplastic polymer comprising dispersed therein at least one amorphous high polymer with a higher glass transition temperature than the glass transition temperature of the thermoplastic polymer and/or at least one crystalline high polymer having a melting point which is higher than the glass transition of the thermoplastic polymer.


According to a tenth embodiment of the printable paper, according to the present invention, said water-resistant support is a non-transparent microvoided axially stretched directly extruded linear polyester having dispersed therein at least one amorphous high polymer having a higher glass transition temperature than that of said linear polyester and/or at least one crystalline high polymer having a higher melting point than the glass transition temperature of said linear polyester matrix, the amorphous high polymer preferably comprising at least one chain-polymerized block.


According to an eleventh embodiment of the printable paper, according to the present invention, said water-resistant support is a non-transparent microvoided axially stretched directly extruded linear polyester having dispersed therein at least one amorphous high polymer having a higher glass transition temperature than that of said linear polyester and/or at least one crystalline high polymer having a higher melting point than the glass transition temperature of said linear polyester matrix, wherein said at least amorphous high polymer is selected from the group consisting of polystyrene, styrene copolymers, SAN-polymers, polyacrylates, acrylate-copolymers, polymethacrylates and methacrylate-copolymers,


According to a twelfth embodiment of the printable paper, according to the present invention, said water-resistant support is a non-transparent microvoided axially stretched directly extruded linear polyester having dispersed therein at least one amorphous high polymer having a higher glass transition temperature than that of said linear polyester and/or at least one crystalline high polymer having a higher melting point than the glass transition temperature of said linear polyester matrix, wherein said crystalline high polymer is selected from the group consisting of polyethylene, preferably high density polyethylene, polypropylene, preferably isotactic polypropylene, and isotactic poly(4-methyl-1-pentene).


According to a thirteenth eleventh embodiment of the printable paper, according to the present invention, said water-resistant support is a non-transparent microvoided axially stretched directly extruded linear polyester having dispersed therein particles of a SAN-polymer and/or at least one crystalline high polymer which has a melting point at a higher temperature than the glass transition temperature of the polyester, with at least one crystalline high polymer selected from the group consisting of high density polyethylene, isotactic polypropylene and isotactic poly(4-methyl-1-pentene) being preferred.


According to a fourteenth embodiment of the printable paper, according to the present invention, said water-resistant support is a non-transparent microvoided axially stretched directly extruded linear polyester having dispersed therein particles of at least one amorphous high polymer with a higher glass transition temperature than the glass transition temperature of the linear polyester and/or isotactic poly(4-methyl-1-pentene), with at least one amorphous high polymer selected from the group consisting of SAN (styrene-acrylonitrile)-polymers and ABS (acrylonitrile-butadiene-styrene)-polymers being preferred.


According to a fifteenth embodiment of the printable paper, according to the present invention, said water-resistant support is a non-transparent microvoided axially stretched directly extruded linear polyester having dispersed therein 5 to 20% by weight of a styrene-acrylonitrile-block copolymer and 0.1 to 10% by weight of isotactic poly(4-methyl-1-pentene).


According to a sixteenth embodiment of the printable paper, according to the present invention, said water-resistant support further comprises an ingredient selected from the group consisting of whitening agents, UV-absorbers, light stabilizers, antioxidants, flame retardants and colorants.


Latex

According to a seventeenth embodiment of the printable paper, according to the present invention, the single layer further comprises a latex, the latex being preferably an anionic acrylic latex or an aliphatic polyurethane latex.


According to an eighteenth embodiment of the printable paper, according to the present invention, the latex is a self-crosslinking latex.


Suitable latexes are given in the table below:






















acid







solids
nr


latex


conc
[mg


nr


[wt %]
KOH/g]
pH
comonomers























01
Joncryl
BASF
42
90
8.5
styrene
2-ethyl-
ammonium



FLX5000





hexyl
acrylate









acrylate









α-methyl-









styrene


02
Joncryl
BASF
32
216 
8.3
styrene
α-methyl-
ammonium



8078





styrene
acrylate


03
Dispercoll
BAYER
40



aliphatic



U53





PU


04
Joncryl
BASF
46
<10  
8.5
styrene
acrylate
ammonium



FLX5010






acrylate


05
Joncryl
BASF
42
111*
7.8
styrene
acrylate
methacrylate



8050


06
Hycar PC84
Dow
48

6.0
styrene
acrylic
acrylonitrile




Chemical




acid
ethyl acrylate










N-hydroxy-










methyl-










acrylamide


07
Carboset
Goodrich
59

6
styrene
acrylate



GA2364


08
Joncryl
BASF
49
16
7.9
quat.
acrylate



8385




mod


09
Enorax
Collano
30

4.5
cationic
PU



PU950


10
wac-17XC
Takamatu
25

8
anionic
polyester




Oil & Fat




PU




Co. Ltd


11
Crom-
Cromogenia-


8.3
cationic
aliphatic



elastic
units




PU



C4480
S.A.


12
Mowilith
Clariant


6
vinyl
veova
acrylate



DM 2452




acetate
(vinyl









versatate)


13
Wellpur
Van Camp
30

5
cationic
aliphatic



FM10C
Chemicals




PU


14
Neorez
Avecia
40

8.3

aliphatic



R989





PU


15
Jetsize
Eka Nobel



cationic
styrene
acrylate



CE225




monomer


16
Hycar
Lubriziol
49



carboxy-



26084





modified









acrylic


17
Hycar 2679
Lubrizol
49


acrylic


18
Hycar 2671
Lubrizol
51



acrylate
acrylonitrile


19
Impranil
BAYER
60



anionic
polyester-



DLU





aliphatic
polyurethane


20
Impranil
BAYER





polyurethane



LP RSC1997


21
Impranil
BAYER





polyurethane



LP RSC3040


22
Bayhydrol
BAYER



XP2558


23
Airflex
Air
60



vinyl
ethylene



EP17
Products




acetate


24
Polysol
Showa
55



vinyl
ethylene



EVA550
Denko K.K.




acetate





*from low-MW alkali-soluble styrene/acrylate copolymer







In the case of those latexes with high pH's and good water and alkaline resistance, it is possible that the latex or a stabilizing dispersing agent is solubilized with ammonium hydroxide and with the evaporation of the ammonia the resins are rendered insoluble.


Suitable self-crosslinking resins are given in the Table below.





















solids





latex


conc
acid nr


nr


[wt %]
[mg KOH/g]
pH
comonomers






















25
Acronal
BASF
50

8.5-10
acrylic




LR 8977


26
Acronal
BASF
50

8.5-10
acrylic



S 760


27
Joncryl
BASF
41

8.3
acrylic



1580


28
Joncryl
BASF
41

8.2
acrylic



8380


29
Joncryl
BASF
40
23
8.1
acrylic



8383


30
Joncryl
BASF
41
27
8.2
acrylic



8384


31
Joncryl
BASF
49
16
7.9
acrylic



8385


32
Joncryl
BASF
40
18
8.0
acrylic



8386


33
Joncryl
BASF
43.5
50
9.6
acrylic



8300


34
Joncryl
BASF
42
26
7.6
acrylic



8311


35
Luhydran
BASF
45
0
 1.5-2.5
acrylic



S 937 T


36
NeoCryl
DSM Neo-



acrylate



XK-98
Resins


37
NeoPac
DSM Neo-



aliphatic
hybrid



R-9029
Resins



urethane










The mechanism of self-crosslinking is not disclosed. However, one skilled in the art would expect crosslinking to be accompanied by insolubilization.


Porous Pigment Particles

According to a nineteenth embodiment of the printable paper, according to the present invention, the porous pigment is an inorganic pigment and includes pigments having primary particles having an internal porosity and pigments whose primary particles have no internal porosity and have a specific surface area of at least 100 m2/g, which are present as secondary particles having an internal porosity as a result of the aggregation of the primary particles. Examples of such primary particles are flame pyrolyzed inorganic particles such as the particles in the Aerosil® range produced by Degussa.


According to a twentieth embodiment of the printable paper, according to the present invention, the at least one porous pigment is an polymeric pigment and includes polymeric pigments having primary particles having an internal porosity and pigments whose primary particles have no internal porosity and have a specific surface area of at least 100 m2/g, which are present as secondary particles having an internal porosity as a result of the aggregation of the primary particles.


According to a twenty-first embodiment of the printable paper, according to the present invention, the at least one porous pigment is a mixture of at least one inorganic porous pigment and at least one organic polymeric porous pigment.


Suitable porous inorganic pigments are given in the table below:





























Oil







Average



absorption






particle

Pore
Pore
capacity


PP-


Chemical
size

volume
diameter
[mL/
Surface


nr
Product name
Producer
composition
[μm]
pH
[mL/g]
[nm]
100 g]
treatment
























01
Sunsphere H53
Asahi Glass
SiO2
5

2
30
400



02
Sunsphere H33
Asahi Glass
SiO2
3

2
30
400


03
Sunsphere H52
Asahi Glass
SiO2
5

2
25
300


04
Sunsphere H32
Asahi Glass
SiO2
3

2
25
300


05
Sunsphere H52
Asahi Glass
SiO2
5

2
25
300


06
Sunsphere H32
Asahi Glass
SiO2
3

2
25
300


07
Sunsphere H51
Asahi Glass
SiO2
5

1
5
150


08
Sunsphere H31
Asahi Glass
SiO2
3

1
5
150


09
Sunsil 130H-SC
Sunjin
SiO2
7

1.4


methicone











treated


10
Sunsil 130SH
Sunjin
SiO2
7

2.2


none


11
Sunsil 130XH
Sunjin
SiO2
7

3.0


none


12
Syloid C803
Grace-
SiO2
3.4-4.0
2.9-3.7
2.0


none




Davison


13
Syloid C807
Grace-
SiO2
6.7-7.9
2.9-3.7
2.0


none




Davison


14
Syloid C2006
Grace-
SiO2
5.4-6.6
3.5
2.0


20%




Davison






special











organic


13
Syloid ED2
Grace-
SiO2
  3.9
6.0



none


15

Davison


16
Syloid ED5
Grace-
SiO2
 8.4-10.2
6.0-8.5
1.8


none




Davison


17
Syloid W500
Grace-
SiO2
7.8-9.4
8.7-9.7
1.2


none




Davison


18
Syloid W300
Grace-
SiO2
5.3-6.3
8.7-9.7
1.2


none




Davison


19
Syloid 72
Grace-
SiO2
4.5-5.7
6.0-8.0
1.2


npne




Davison


20
Syloid 74
Grace-
SiO2
5.9-7.5
6.0-8.0
1.2


none




Davison


21
Syloid 244
Grace-
SiO2
2.5-3.7
6.0-8.0
1.6


none




Davison


22
Spheron L1500
CCIC/Ikeda
SiO2
 3-15

1.46


23
Spheron P1500
CCIC/Ikeda
SiO2
7

0.65-0.7


24
ZeeoSphere
3M
SiO2;
5
>3


70



G200

Al2O3


25
Micral 9400
J. M. Huber
Al(OH)3


26
Digitex 1000
Engelhard
Kaolin-




Industries
based





pigment


27
Syloid SP500-
Grace-
SiO2



11007
Davison









Suitable porous polymeric pigments are given in the table below:
























Average



Oil absorption






particle

Pore
Pore
capacity


PP-


Chemical
size

volume
diameter
[mL/


nr
Product name
Producer
composition
[μm]
pH
[mL/g]
[nm]
100 g]







28
Submicron
Nippon
urea-form-
1-8#



500-1000



Filler
Kasei
aldehyde





resin


29
Micropearl
Matsumoto
PMMA
4.3

0.45



M305


30
Covabead LH170
LCW
PMMA
7.2

1.7 


31
Sunpmma-PH
Sunjin
PMMA
8

2.3-2.6
17
2.2


32
Deuteron OG874
Deuteron
ground

8.0





polymethyl





urea


33
Pergopak M6
Albemarle
polymethyl
0.3*





urea


34
Pergopak HP
Albemarle
polymethyl
0.125*





urea





#primary particle size 0.1-0.3 μm


*primary particle size






Porosity can be determined by standard techniques such as nitrogen porosimetry, in which nitrogen is condensed in the pores and calculating the pore volumes from the quantities of gas required to fill the pores, and mercury porosimetry, in which liquid mercury is forced into pores by increasing the external pressure, the amount of mercury required to fill the pores being increased incrementally.


Opacifying Pigments

According to a twenty-second embodiment of the printable paper, according to the present invention, the single layer further comprises at least one opacifying pigment.


Suitable opacifying pigments are given in the table below:





























Oil







Average



absorption






particle

Pore
Pore
capacity


OP-


Chemical
size

volume
diameter
[mL/
Surface


nr
Product name
Producer
composition
[μm]
pH
[mL/g]
[nm]
100 g]
treatment







01
SpaceRite S-11
Almatis
Al(OH)3
0.25-0.31
9.8


24-28



02
Pural BT
Sasol
Al(OH)3
5


03
Carbital 110
Zinchem
CaCO3
2


04
Carbital 120
Zinchem
CaCO3
5


05
Jetcoat 30
Specialty
CaCO3

7.0




Minerals
slurry


06
VPR350ME
SA Omya
CaCO3

6.5




Benelux
anionic





slurry


07
China Clay
Engelhard
China Clay
0.4
3.5-5.0 



Pigment ASP200
Industries


08
China Clay
Zinchem
China Clay
2



Grade B


09
Snowtex
Nissan
colloidal
10-20 nm
9.0-10.5




Chemical
SiO2


10
Hydragloss 90
J. M. Huber
fine





glossing





coating





clay


11
Artnr. 102143
Merck
Ca5(PO4)3OH


12
VITOSS
Orthovita
Ca3(PO4)2
0.1*


13
Kronos 2059
Kronos
TiO2

7.0


18-21


14
Ti Pure R900
Du Pont
TiO2
4
7.3


15
Finntitan RD5
Keyser &
TiO2
0.21
7.5


19




Mackay









Water-Soluble Binder

According to a twenty-third embodiment, of the printable paper, according to the present invention, the single layer further comprises at least one water-soluble binder.


According to a twenty-fourth embodiment, of the printable paper, according to the present invention, the water-soluble binder is a hydrolyzed polymer or copolymer of a vinylester.


According to a twenty-fifth embodiment, of the printable paper, according to the present invention, the water-soluble binder is a hydrolyzed polymer or copolymer of vinyl acetate, with a degree of hydrolysis of at least 85% being preferred, and a degree of hydrolysis of at least 87% being particularly preferred.


Suitable water-soluble binders include the hydrolyzed polyvinyl acetates given in the table below.
















Degree of
Residual acetyl



hydrolysis
(Vinyl acetate)



[mol %]
content [wt %]




















B01
Erkol 48 20
ACETEX
97.5-99.5



B02
Mowiol 10-74
Kuraray
74  




Specialties




Europe




(KSE)


B03
Airvol 350
Air
97.5-99.5




Products


B04
Airvol 540
Air
87-88




Products


B05
Mowiol 15-79
KSE
81.5
15.4


B06
Mowiol 3-83
KSE
82.6
14.6


B07
Mowiol 4-88
KSE
87.7
10.8


B08
Mowiol 5-88
KSE
87.7
10.8


B09
Mowiol 8-88
KSE
87.7
10.8


B10
Mowiol 18-88
KSE
87.7
10.8


B11
Mowiol 23-88
KSE
87.7
10.8


B12
Mowiol 26-88
KSE
87.7
10.8


B13
Mowiol 40-88
KSE
87.7
10.8


B14
Mowiol 47-88
KSE
87.7
10.8


B15
Mowiol 30-92
KSE
92.4
6.9


B16
Mowiol 3-96
KSE
97.2
2.7


B17
Mowiol 3-98
KSE
98.4
1.5


B18
Mowiol 6-98
KSE
98.4
1.5


B19
Mowiol 10-98
KSE
98.4
1.5


B20
Mowiol 20-98
KSE
98.4
1.5


B21
Mowiol 56-98
KSE
98.4
1.5


B22
Mowiol 28-99
KSE
99.4
0.6


B23
Poval PVA 203
Kuraray
88.0


B24
Poval PVA 205
Kuraray
87.8


B25
Poval PVA 217
Kuraray
88.0


B26
Poval PVA 220
Kuraray
88.0


B27
Poval PVA 224
Kuraray
88.0


B28
Poval PVA 226
Kuraray
87.5


B29
Poval PVA 235
Kuraray
88.0


B30
Poval PVA 403
Kuraray
80.0


B31
Poval PVA 405
Kuraray
81.5


B32
Poval PVA 420
Kuraray
79.5


B33
Poval PVA CST
Kuraray
96.0


B34
Poval PVA 613
Kuraray
93.5


B35
Poval PVA 624
Kuraray
95.5


B36
Poval PVA 706
Kuraray
91.5


B37
Poval PVA 103
Kuraray
98.5


B38
Poval PVA 105
Kuraray
98.5


B39
Poval PVA 110
Kuraray
98.5


B40
Poval PVA 117
Kuraray
98.5


B41
Poval PVA 124
Kuraray
98.5









Hardened Polyhydroxy-Resin

According to a twenty-sixth embodiment, of the printable paper, according to the present invention, the single layer further comprises at least one hardened initially water-soluble polyhydroxy resin.


According to a twenty-seventh embodiment of the present invention, the single layer further contains a hardened hydrolyzed polymer or copolymer of a vinyl ester e.g. by the hardening of POVAL R1130, a silanol modified polyvinyl alcohol.


Suitable water-soluble polyhydroxy resins include hydrolyzed polymers or copolymers of a vinylester; cellulose and cellulose derivatives; polysaccharides; and polyalkylene glycols.


Suitable hardeners include polyisocyanates, hydrolyzed polyalkoxysilanes e.g. tetraalkyl orthosilicates.


Insolubilization Agents

Insolubilization is a process in which either a solublization process is reversed e.g. by pH reduction if a pH-change brings about solublization e.g. by conversion of a carboxy group into a carboxylate ion e.g. by acidification or simple evaporation of ammonia if ammonium hydroxide is used to realize the solubilization. Such solubilization can apply to a latex or to a dispersing agent stabilizing a latex dispersion. Alternatively insolublization can be the addition of an insolubilizing agent such as formaldehyde, glutaraldehyde, glyoxal, glyoxal-derivatives, dimethylol urea, polyanionic metallic compounds (see GB 2177413A at page 2, line 5) and melamine-formaldehyde resins and carboxylic acid anhydrides which contain a plurality of anhydride moieties on each molecular entity (see U.S. Pat. No. 6,300,393). These insolubilization agents can catalyze, initiate a reaction with, complex with, cure or otherwise react with the species being insolubilized. Moreover, the insolubilizing agent may require activation in order for it to acquire insolubilizing properties e.g. by heating, exposure to electromagnetic radiation e.g. light, X-rays, electron beams etc., a change in pH or any other means.


According to a twenty-eighth embodiment of the printable paper, according to the present invention, the single layer further comprises at least one insolubilizing agent unless said latex is solubilized with ammonium hydroxide.


According to a twenty-ninth embodiment of the printable paper, according to the present invention, the single layer further comprises at least one insolubilizing agent selected from the group consisting of: polyisocyanates, formaldehyde, formaldehyde derivatives, glutaraldehyde, glyoxal, glyoxal-derivatives, dimethylol urea, polyanionic metallic compounds and melamine-formaldehyde resins, polyalkoxysilanes (e.g. tetraalkyl orthosilicates), and carboxylic acid anhydrides which contain a plurality of anhydride moieties on each molecular entity.


Suitable insolubilizing agents include:















IN01:
Bayhydur 3100, a hydrophilic aliphatic isocyanate based on



hexamethylene diisocyanate (HDI from Bayer


IN02:
Parez Resin 707, a dimethylol trimethylolmelamine formaldehyde



resin from Am Cyanamid


IN03:
Irgacure 500, a hydrophilic aliphatic isocyanate based on



hexamethylene diisocyanate (HDI from Bayer


IN04:
Bayhydur XP2547, a hydrophilic aliphatic isocyanate based on



hexamethylene diisocyanate (HDI from Bayer


IN05:
Irgacure 819DW, a UV-initiator from CIBA


IN06:
Irgacure 500, a UV-initiator from CIBA


IN07:
Berset ® 2115*, a glyoxal-based reactant as a light straw-



coloured liquid (46-48 wt %) from Bercen, Inc.


IN08:
Berset ® 2116*, a glyoxal-based reactant as a clear straw-



coloured liquid (49-51 wt %)from Bercen, Inc.


IN09:
Berset ® 2125*, a glyoxal-based reactant as a light straw-



coloured liquid (67-69 wt %)from Bercen, Inc.


IN10:
Berset ® 2185*, a glyoxal-based reactant from Bercen, Inc.


IN11:
Berset ® 2506*, a melamine-formaldehyde resin as a clear to



slightly hazy liquid (69-71 wt %) from Bercen, Inc.


IN12:
Berset ® 2700*, a cyclic amide condensate as a clear amber



solution (44-46 wt %) from Bercen, Inc.


IN13:
Berset ® 2720*, a ammonium zirconium carbonate as a clear to



slightly hazy solution (30.5-33.5 wt %)# from Bercen, Inc.


IN14:
Berset ® 2750*, a potassium zirconium carbonate as a clear to



slightly hazy solution (45-50 wt %) from Bercen, Inc.





*supplied by


#also available from Magnesium Elektron Ltd., Twickenham, England.






Matting Agents

According to a thirtieth embodiment of the printable paper, according to the present invention, the single layer further comprises a matting agent.


Suitable matting agents are given in the table below:















MA01:
a 7-8 μm grafted polymethylmethacrylate matting agent


MA02:
a 3-12 μm polyethylene wax


MA03:
Syloid C907, 7 μm silica particles from Grace-Davison


MA04:
Pergopak M, 6-20 μm polymethylurea particles from



Albemarle


MA05:
Syloid SP4-9701, 11 μm silica particles from Grace-Davison


MA06:
PMMA 10, 10 μm polymethylmethacrylate particles from



H.W. Sands


MA07:
PMMA 10TIGHT, 10 μm crosslinked polymethylmethacrylate



particles from H.W. Sands


MA08:
EPOSTAR L15, 10-15 μm benzoguanine-melamine/



formaldehyde particles from Nippon Shokubai


MA09:
Orgasol 3501 EXD NAT1, 10 μm polyamide particles from



Atochem S.A.


MA10:
Flo Beads EA209, 10 μm ethylene-acylic acid copolymer



particles from Sumitomo,


MA11:
Flo Beads CL2080, 12.5 μm polyethylene particles from



Sumitomo


MA12:
Tospearl 3120, 12 μm polydimethylsiloxane particles from



Toshiba


MA15
a 6 μm grafted polymethylmethacrylate matting agent









Preservative

According to a thirty-first embodiment of the printable paper, according to the present invention, the single layer further comprises a preservative. The purpose of a preservative is to act as a bactericide and fungicide to prevent the growth of mould.


According to a thirty-second embodiment of the printable paper, according to the present invention, further comprises a salt of 1,2-benzisothiazolin-3-one e.g. the sodium salt of 1,2-benzisothiazolin-3-one commercially available under the trade name “Proxel” and Bronidox K.


Process for Producing a Printable Paper

Aspects of the present invention are realized by a process for producing a printable paper comprising the steps of: (i) optionally providing a water-resistant support having two sides with a subbing layer on at least one side; (ii) providing at least one side of said optionally subbed water-resistant support with a single layer having no substantial compositional variation, said single layer being applied to said optionally subbed water-resistant support as at least one wet aqueous layer in a single pass for each side of said water-resistant support, said at least one aqueous layer comprising at least one latex, at least one pigment, at least one binder and optionally at least one insolubilizing agent, wherein said latex is an anionic acrylic latex or an aliphatic polyurethane latex.


INDUSTRIAL APPLICATION

Non-transparent microvoided axially stretched films, according to the present invention, can be used as synthetic paper for printing and other applications, as a relector in LCD displays and photovoltaic devices, as a support for imaging materials e.g. impact and non-impact (e.g. electrophotography, electrography and ink jet) receiving materials, photothermographic recording materials, substantially light-insensitive thermographic recording materials, dye sublimation printing, thermal transfer printing, etc., in security and anti-counterfeiting applications e.g. in tickets, labels, tags, an ID-card, a bank card, a legal document, banknotes and packaging and can also be integrated into packaging.


The invention is illustrated hereinafter by way of comparative examples and examples. The percentages and ratios given in these examples are by weight unless otherwise indicated.


Ingredients used in the EXAMPLES and COMPARATIVE EXAMPLES:


Slipping agents:






    • SL01: Tegoglide 482 a 65% by weight aqueous emulsion of a high molecular weight polydimethylsiloxane surfactant from Goldschmidt


      Surfactants:

    • S01: Synperonic 91/5, an alcohol ethoxylate with the composition C9-11H19-23O—(C2H4O)5H from Uniqema;

    • S02: MERSOLAT®H, a sodium pentadecylsulfonate from BAYER;

    • S03: ULTRAVON®W, a sodium arysulfonate from CIBA [UVONAC];

    • S04: DR247

    • S05: Arkopon T, a sodium salt of N-methyl-N-2-sulfoethyl-oleylamide supplied as a 40% concentrate by Avecia [OTIK];

    • S06: Envirogem AE01 a 100% mixture of esters from Air Products

    • S07: Zonyl FS0100 a mixture of ethoxylated non-ionic fluoro-surfactant from DuPont with the formula:

      F(CF2CF2)1-7CH2CH2O(CH2CH2O)yH where y=0 to ca. 15 from DuPont

    • POLYESTER:
























Inherent






MFI 270° C./
viscosity**


PET-


1.20 kg
[η]
Tg


nr


[cm3/10 min]
[dl/g]
[° C.]




















01
T03*
polyethylene terephthalate
34.8
0.60
80.5


02
T04*
polyethylene terephthalate
34.8
0.60
80.5


03
WP75#
polyester of 98.5 mol % terephthalate,

0.77
80




1.5 mol % isophthalate




and 100 mol % ethylene units


04
DP9990#
polyester of 90 mol % terephthalate,

0.60




10 mol % isophthalate




and 100 mol % ethylene units





*AGFA-GEVAERT N.V.


#La Seda


**inherent viscosity was determined in a 0.5 g/dL solution of 60 wt % phenol and 40 wt % ortho-dichlorobenzene at 25° C. in an Ubbelohde viscometer








    • STYRENE-ACRYLONITRILE COPOLYMERS:
























Wt %

MFI at





SAN-

acrylo-
Wt %
270° C./1.20 kg


Tg


nr

nitrile
styrene
[mL/10 min]
Mn
Mw
[° C.]






















01
TYRIL 905*
20
80
7.1


105.2


02
TYRIL 867E*
25
75
5.8


106.5


03
SAN 140*
27.5
72.5
53.2
47,640
99,820
108.8


04
LURAN 368R#
28
72
3.9


107.3


05
TYRIL 790*
29
71
12.1


106.3


06
SAN 124*
28.5
71.5
37.9
53,940
109,350
108.1


07
LURAN 388S#
33
67
3.6


108.7





*DOW CHEMICAL


#BASF


MFI = Melt Flow Index








    • TITANIUM DIOXIDE: Renol-white/PTX 506, a masterbatch from CLARIANT GmbH containing 65% by weight TiO2 and 35 wt % polyester

    • TPX DX820: a high rigidity isotactic poly(4-methyl-1-pentene) from MITSUI CHEMICAL





Examples 1 and 2
Production of Subbed Supports

A ca. 1100 μm thick extrudate with the composition given in Table 1 below was biaxially stretched according to the conditions given in Table 2 to provide a non-transparent microvoided biaxially stretched self-supporting film with a thickness of 150 μm.
















TABLE 1












UVITEX


EXAMPLE
IPA:TPA
PET02
PET04
SAN 06
TiO2
TPX 820
OB-one


nr
ratio
[wt %]
[wt %]
[wt %]
[wt %]
[wt %]
[wt %]






















1
0.0769
23.734
59.30
15.00
1.95

0.0260


2
0.0769
23.613
59.00
14.92
1.945
0.497
0.0259




















TABLE 2









Longitudinal





stretching
Transversal stretch













EXAMPLE

force
temperature

speed
Density


nr
ratio
[N/mm2]
[° C.]
ratio
[%/min]
[g/mL)





1/LS1/BS1
3.3
12
110
3.5
1000
1.2


2/LS1/BS1
3.3
12
110
3.5
1000
1.2









The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 and 2/LS1/BS1 were then subbed with subbing layers 1, a non-antistatic layer, subbing layer 2, an antistatic subbing layer composition, subbing layer 3, an antistatic subbing layer composition, subbing layer 4, a non-antistatic layer composition or subbing layer 5, an antistatic layer composition, on one or both sides of the support:












Subbing layer 1:









coverage in



dried layer



[mg/m2]














copolymer of 88% vinylidene chloride, 10%
79.1



methyl acrylate and 2% itaconic acid



Kieselsol ® 100F, a colloidal silica from BAYER
18.6



Surfactant No. 2, an anionic surfactant
0.4



Surfactant No. 3, an anionic surfactant
1.9




















Subbing layer 2:









coverage in



dried layer



[mg/m2]












poly(3,4-ethylenedioxythiophene)/polystyrene sulphonic
2.58


acid (1:2.46 by weight)


Bronidox K
0.02


copolymer of 88% vinylidene chloride, 10% methyl
147.3


acrylate and 2% itaconic acid stabilized with surfactant S05


Kieselsol ® 100F, a colloidal silica from BAYER
16.4


sorbitol
[24.7*]


Surfactant S02, an anionic surfactant
0.74





*will substantially evaporate/sublime during the drying process
















Subbing layer 3:










wt %




solids
coverage in



in coating
dried layer



dispersion
[mg/m2]













poly(3,4-ethylenedioxythiophene)/polystyrene
6.01
 2.838


sulphonic acid (1:2.46 by weight)


sorbitol
28.06
[13*]  


Proxel Ultra 5
0.03
0.01


Surfactant S01, a non-ionic surfactant
1.66
0.78


a terephthalic acid, isophthalic acid, 5-sulfo-
64.24
30.2 


isophthalic acid, ethylene glycol (53:40:7:100


molar ratio) copolyester





*will substantially evaporate/sublime during the drying process
















Subbing layer 4:









coverage in



dried layer



[mg/m2]












copolymer of 88% vinylidene chloride, 10% methyl
80.85


acrylate and 2% itaconic acid stabilized with surfactant S05


Kieselsol ® 100F, a colloidal silica from BAYER
18.75


Surfactant S02, an anionic surfactant
0.4



















Subbing layer 5:










wt %
coverage



solids
in



in coating
dried layer



dispersion
[mg/m2]













poly(3,4-ethylenedioxythiophene)/polystyrene
1.30
4.69


sulphonic acid (1:2.46 by weight)


copolymer of 88% vinylidene chloride, 10%
82.16
294.54


methyl acrylate and 2% itaconic acid stabilized


with surfactant S05


Kieselsol 100F-30, a colloidal silca from BAYER
9.13
32.72


Surfactant S02, an anionic surfactant
0.30
0.11


glucose
6.94
[24.9*]


Proxel Ultra 5
0.005
0.03


sorbitol
0.16
[0.57*]





*will substantially evaporate/sublime during the drying process






Optimalization of the Receiving Layer Composition
Example 3
Screening of Different Latexes

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 1 was coated with the compositions in Table 3 in the case of EXAMPLES 3/1 to 3/3 together with small quantities of Tego Glide 482, a high molecular weight polydimethylsiloxane from Goldschmidt, and the surfactant S04; in the case of EXAMPLES 3/4 to 3/8 just with quantities of the surfactant S04; in the case of EXAMPLES 3/9 to 3/19 with a mixture of two surfactants (S04 and S05); in the case of EXAMPLES 3/20 to 3/28 with a mixture of two surfactants (S05 and S06); in the case of EXAMPLES 3/26; in the case of EXAMPLES 3/27 to 3/31 without further additives; and in the case of EXAMPLES 3/32 to 3/38 with a mixture of two surfactants (S05 and S06).















TABLE 3









Porous

Wt ratio





pigment
Latex
porous

printing properties
















Example

coverage

coverage
pigment
ballpen
dry time




nr
nr
[mg/m2]
nr
[g/m2]
to latex
writability
[min]
set-off
mottle



















3/1
PP21
760
01
2000
0.380
repulsion











in centre


3/2
PP21
760
PAZ
2000
0.380
v. good


3/3
PP21
760
02
2000
0.380
good


3/4
PP21
762
01
2031
0.375
good


3/5
PP21
762
02
2031
0.375
repulsion








in centre


3/6
PP21
762
MS16826
2031
0.375
good
5
no


3/7
PP21
762
MS5291
2031
0.375
repulsion








in centre


3/8
PP21
762
L23
2031
0.375

5
no


3/9
PP21
762
01
2031
0.375
repulsion

strong
yes








in centre


3/10
PP21
2031
01
2031
1.00
good

no
slight


3/11
PP21
1500
01
2031
0.739
moderate

no
slight








density


3/12
PP21
762
L24
2031
0.375
v.

yes
strong








moderate








density


3/13#
PP21
1500
L24
2031
0.739
good

no
slight


3/14
PP21
762
L23
2031
0.375
repulsion

no
slight








in centre


3/15#
PP21
1500
L23
2031
0.739
repulsion

no
no








in centre


3/16
PP21
762
04
2031
0.375
repulsion

strong
yes








in centre


3/17
PP21
1500
04
2031

v. good

yes
yes


3/18
PP21
762
05
2031
0.375
repulsion

strong
yes








in centre


3/19
PP21
1500
05
2031
0.739
repulsion

no
no








in centre


3/20
PP21
990
01
2010
0.491
repulsion

slight
yes








in centre


3/21*
PP21
990
L23
2010
0.491


no
slight


3/22
PP21
990
06
2010
0.491


slight
yes


3/23
PP21
990
07
2010
0.491


slight
yes


3/24
PP21
1500
MS60054
2031
0.739


yes
yes


3/25
PP21
762
05
2031
0.375


yes
slight


3/26
PP21
1500
05
2031
0.739


no


3/27##
PP21

B01




no
slight


3/28**
PP21

B01




no
no


3/29***
PP21

B01




no
no


3/30#
PP21
750
MS16357
2000
0.375



yes


3/31#
PP21
1500
MS16357
2000
0.750



no


3/32
PP21
750
CP3077
2000
0.375


yes
no


3/33
PP21
750
CE1611
2000
0.375


yes
slight


3/34
PP21
1500
CE1611
2000
0.750


yes
no


3/35
PP21
1000
08
2000
0.500


slight
yes


3/36
PP21
1000
09
2000
0.500


slight
yes


3/37
PP21
1000
10
2000
0.500


strong
yes


3/38****
PP21
1000
10
2000
0.500


v.
no










strong





#poor adhesion


*not scratch-resistant PAZ = MS16686


##hardened with 100% glyoxal at pH 4


**hardened with 50% tetramethyl orthosilicate at pH 4


***hardened with 100% tetramethyl orthosilicate at pH 4


****hardened with 0.999 g/m2 MS15262







MS16357 POVAL R1130


A lack of adhesion between the support and the single layer is remediable by adapting the modifying the subbing layer or by providing a subbing layer comprising the plurality of subbing layers required to realize adhesion between the support and the single layer.


Example 4
Screening of Different latexes

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 4 with 0.04 g/m2 of the surfactant S07.














TABLE 4









Porous






pigment
Latex
Wt ratio
Binder
















cover-

cover-
porous

cover-




age

age
pigment

age


Example nr
nr
[g/m2]
nr
[g/m2]
to latex
nr
[g/m2]

















4/1
PP21
1.5
L04
2.0
0.75




4/2
PP21
2.0
L04
2.0
1.0




4/3
PP21
2.0
L04
2.0
1.0
B01
0.2


4/4
PP21
1.5
L32
2.0
0.75




4/5
PP21
2.0
L32
2.0
1.0




4/6
PP21
2.0
L32
2.0
1.0
B01
0.2


4/7
PP21
1.5
L20
2.0
0.75




4/8
PP21
2.0
L20
2.0
1.0




4/9
PP21
2.0
L20
2.0
1.0
B01
0.2


4/10
PP21
1.5
L19
2.0
0.75




4/11
PP21
2.0
L19
2.0
1.0




4/12
PP21
2.0
L19
2.0
1.0
B01
0.2


4/13
PP21
1.5
L22
2.0
0.75




4/14
PP21
2.0
L22
2.0
1.0




4/15
PP21
2.0
L22
2.0
1.0
B01
0.2


4/16
PP21
2.0
L04
2.0
1.0
B01
0.2


4/17
PP21
2.0
L04
2.0
1.0
B01
0.2


4/18
PP21
1.5
04
2.0
0.75




4/19
PP21
2.0
04
2.0
1.0




4/20
PP21
2.0
04
2.0
1.0
B01
0.2


4/21
PP21
1.5
L16
2.0
0.75




4/22
PP21
2.0
L16
2.0
1.0




4/23
PP21
2.0
L16
2.0
1.0
B01
0.2


4/24
PP21
1.5
L17
2.0
0.75




4/25
PP21
2.0
L17
2.0
1.0




4/26
PP21
2.0
L17
2.0
1.0
B01
0.2


4/27
PP21
1.5
L18
2.0
0.75




4/28
PP21
2.0
L18
2.0
1.0




4/29
PP21
2.0
L18
2.0
1.0
B01
0.2


4/30*
PP21
2.2
L21
2.14
0.973
B01
 0.22





*MMA01 in concentration of 0.1 g/m2






Printing tests were carried out on a Heidelberg GTO46 printing press with a K+E800 ink and as fountain 4% AGFA FS330 with 10% isopropanol. The results of qualitative printability tests are summarized in Table 5.












TABLE 5










IGT




tests



Printing tests
drying
















Wt ratio



Dot
time to




porous



gain
avoid


Example

pigment
ballpen
Tape test

50%
set-off


nr
Latex
to latex
writability
dry [10 min]
mottle
screen
[s]

















4/1
L04
0.75
repulsion
OK
yes
24
>58





in centre


4/2
L04
1.0
repulsion
cohesive
no
25
48





in centre
break


4/3
L04
1.0
repulsion
OK
no
25
31





in centre


4/4
L32
0.75
repulsion
OK
yes
26
31





in centre


4/5
L32
1.0
repulsion
OK
slight
25
31





in centre


4/6
L32
1.0
good
OK
no
25
9


4/7
L20
0.75
repulsion
cohesive
yes
26





in centre
break


4/8
L20
1.0
repulsion
delaminates
yes
25





in





centre/cracking


4/9
L20
1.0
repulsion
OK
yes
24





in





centre/





cracking


4/10
L19
0.75
good
delaminates


4/11
L19
1.0
good
delaminates


4/12
L19
1.0
repulsion
delaminates





in centre


4/13
L22
0.75
repulsion
OK





in centre/





cracking


4/14
L22
1.0
repulsion
cohesive





in centre
break


4/15
L22
1.0
repulsion
OK





in centre


4/16
L04
1.0

OK
no
25


4/17
L04
1.0

OK
no
26


4/18
04
0.75

OK
strong
29


4/19
04
1.0

slight
strong
27






cohesive






break


4/20
04
1.0

OK
no
27


4/21
L16
0.75

OK
slight
28


4/22
L16
1.0

strong
no
26






cohesive






break


4/23
L16
1.0

slight
no
25






cohesive






break


4/24
L17
0.75

delaminates
slight
29


4/25
L17
1.0

delaminates
strong
27


4/26
L17
1.0

OK
slight
27


4/27
L18
0.75

delaminates
strong
27


4/28
L18
1.0

delaminates
no
27


4/29
L18
1.0

strong
no
27






cohesive






break


4/30*
L21
0.973

OK
no
27





*Linimark evaluation of scratch resistance carried out with a Roberta apparatus gave a force before scratching was observed of 31 mN






Table 6 summarize the findings of EXAMPLES 3 and 4 in respect of the choice of latex for use in the single layer coated on at least on side of an optionally subbed support.










TABLE 6





latex



nr


















01
Joncryl
BASF
REFERENCE; pH 8.5; poor mottle; no



FLX5000

alkali resistance; water resistant





[fensterklar]


02
Joncryl
BASF
cf. FLX 5000; pH 8.3; ammonia-



8078

neutralized; poor mottle; non alkali-





resistant; poorer drying than REF;





poor adhesion


03
Joncryl
BASF
pH 8.5; better alkali-resistance; poor



FLX5010

mottle; water resistant


04
Joncryl
BASF
cf. FLX 5000; pH 7.8; partially



8050

neutralized resin; with as emulsifier





a low-molecular-weight alkali-soluble





styrene/acrylate copolymer; poor





mottle; non alkali-resistant


05
Hycar
Dow
pH 6.0; cf. FLX 5000; poor mottle; non



PC84
Chemical
alkali-resistant; self-crosslinking


06
Carboset
Goodrich
PH 5.5, 6.5; cf. FLX 5000; poor



GA2364

mottle; non alkali-resistant


07
Joncryl
BASF
pH 7.9; self-crosslinking; cf. FLX



8385

5000; poor mottle; no alkali





resistance


08
Enorax
Collano
pH 4.5; very good (better than FLX



PU950

5000); no longer commercially





available


09
wac-17XC
Takamatu
pH 7, 9; cf. FLX 5000; poor mottle; no




Oil & Fat
alkali resistance




Co. Ltd


10
Crom-
Cromogenia-
pH 8.3; cf. FLX 5000; better mottle;



elastic
units
no alkali resistance



C4480
S.A.


11
Mowilith
Clariant
pH 5, 7; cf. FLX 5010; no alkali



DM 2452

resistance


12
Wellpur
Van Camp
pH 4, 6; no mottle; alkali resistant;



FM10C
Chemicals
layer appears flocked; rough to touch


13
Neorez
Avecia
pH 8.3; cf. FLX 5000; no alkali



R989

resistance; mottle better


14
Jetsize
Eka Nobel
cf. FLX 5010; better alkali-



CE225

resistance; poor mottle









Example 5
Screening of Different Porous pigments

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 1 was coated with the compositions in Table 7 in the case of EXAMPLES 5/1 to 5/15 together with small quantities of Tego Glide 482, a high molecular weight polydimethylsiloxane from Goldschmidt, and surfactant S04; in the case of EXAMPLES 5/16 to 5/xx with















TABLE 7









Porous

Wt ratio





pigment
Latex
porous

printing properties
















Example

coverage

coverage
pigment
ballpen
dry time
set-



nr
nr
[mg/m2]
nr
[g/m2]
to latex
writability
[min]
off
mottle



















5/1
PP21
76
01
203
0.374
repulsion











in centre


5/2


01
203

no


5/3
PP13
76
01
203
0.374
good


5/4
OP03
76
01
203
0.374
v. poor


5/5
OP04
76
01
203
0.374
poor


5/6
OP07
76
01
203
0.374
poor


5/7
OP08
76
01
203
0.374
poor


5/8
OP11
76
01
203
0.374
good


5/9
PP21
760
01
2000
0.380
repulsion








in centre


5/10
PP21
1500
01
2000
0.750
repulsion








in centre


5/11
PP21
2000
01
2000
1.00 
denser
5
no








but








repulsion








in centre


5/12
OP13
760
01
2000
0.380
no


5/13
PP21
375
01
2000
0.188
v. poor



OP13
375


0.188


5/14
OP13
760
01
2000
0.380
v. poor









Example 6
Screening of Different Porous Pigments

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 8 with in the case of EXAMPLES 6/1 to 6/38 with a mixture of two surfactants (S05 and S06).













TABLE 8










Wt ratio



Ex-
Porous pigment
Latex
porous
Binder














ample

coverage

coverage
pigment

coverage


nr
nr
[g/m2]
nr
[g/m2]
to latex
nr
[g/m2]

















6/1
PP21
1.5
L05
2.0
0.75




6/2
PP21
0.75
L05
2.0
0.375




6/3
PP21
0.75
L05
2.0
0.375





OP06
0.25


6/4
PP21
0.75
L05
2.0
0.375





OP06
0.50


6/5
PP21
0.75
L05
2.0
0.375





OP06
0.75


6/6
OP06
0.75
L05
2.0





6/7
OP06
0.25
L05
2.0





6/8
PP21
1.5
L01
2.0
0.75




6/9
PP21
2.0
L01
2.0
1.0




6/10
PP01
1.5
L01
2.0
0.75




6/11
PP01
2.0
L01
2.0
1.0




6/12
PP02
1.5
L01
2.0
0.75




6/13
PP02
2.0
L01
2.0
1.0




6/14
PP21
1.0
L01
2.0
0.5




6/15
PP21
1.5
L01
2.0
0.75




6/16
PP21
2.0
L01
2.0
1.00




6/17
OP01
1.0
L01
2.0
0.5




6/18
OP01
1.5
L01
2.0
0.75




6/19
OP01
2.0
L01
2.0
1.00




6/20
OP02
1.0
L01
2.0
0.5




6/21
OP02
1.5
L01
2.0
0.75




6/22
OP02
2.0
L01
2.0
1.00




6/23
PP28
1.0
L01
2.0
0.5




6/24
PP28
1.5
L01
2.0
0.75




6/25
PP28
2.0
L01
2.0
1.00




6/26
PP21
1.5
L01
2.0
0.75




6/27
PP21
1.0
L01
2.0
0.75





PP28
0.5


6/28
PP21
0.75
L01
2.0
0.75





PP28
0.75


6/29
PP21
0.5
L01
2.0
0.75





PP28
1.0


6/30
PP28
1.5
L01
2.0
0.75




6/31
PP21
1.0
L01
2.0
0.75





PP02
0.5


6/32
PP21
0.75
L01
2.0
0.75





PP02
0.75


6/33
PP21
0.5
L01
2.0
0.75





PP02
1.0


6/34
PP02
1.5
L01
2.0
0.75




6/35
PP21
1.5
L01
2.0
0.75




6/36
PP15
1.5
L01
2.0
0.75




6/37
PP12
1.5
L01
2.0
0.75




6/38
PP28
1.5
L01
2.0
0.75











Printing tests were carried out on a A.B. Dick D9890 printing press with a K+E800 ink and as fountain 4% Emerald Premium with 10% isopropanol and an IGT Global Standard Tester 2. The results are summarized in Table 9.













TABLE 9









Weight
Printing tests
IGT tests

















ratio


Dot
penetration

time to




porous


gain
test
penetration
avoid


Example
Porous
pigment


50%
length
test
set-off


nr
pigments
to latex
set-off
mottle
screen
[mm]
OD
[s]


















6/1
PP21
0.75
no
yes






6/2
PP21
0.375
v.
yes





strong


6/3
PP21
0.375
strong
yes



OP06


6/4
PP21
0.375
yes
yes



OP06


6/5
PP21
0.375
slight
yes



OP06


6/6
OP06

very
yes





strong


6/7
OP06

yes
yes


6/8
PP21
0.75

yes

125.0


6/9
PP21
1.0

slight

103.0


6/10
PP01
0.75

slight

88.7


6/11
PP01
1.0

slight

89.7


6/12
PP02
0.75

slight

106.3


6/13
PP02
1.0

ca. no

94.3


6/14
PP21
0.5

yes


6/15
PP21
0.75

yes


6/16
PP21
1.00

slight


6/17
OP01
0.5
v.
?





strong


6/18
OP01
0.75
v.
?





strong


6/19
OP01
1.00
v.
?





strong


6/20
OP02
0.5
strong
yes


6/21
OP02
0.75
strong
no


6/22
OP02
1.00
strong
no


6/23
PP28
0.5

slight


6/24
PP28
0.75

no


6/25
PP28
1.00

no


6/26
PP21
0.75
yes
yes

111.0


6/27
PP21
0.75
yes
no

90.0



PP28


6/28
PP21
0.75
no
no

84.3



PP28


6/29
PP21
0.75
no
no

87.3



PP28


6/30
PP28
0.75
no
no

76.3


6/31
PP21
0.75
no
yes

124.3



PP02


6/32
PP21
0.75
no
slight

110.3



PP02


6/33
PP21
0.75
no
slight

108.3



PP02


6/34
PP02
0.75
no
slight

104.3


6/35
PP21
0.75
no
yes

121.3


6/36
PP15
0.75
slight
yes

142.0


6/37
PP12
0.75
slight
yes

120.0


6/38
PP28
0.75
slight
yes

131.0









Replacement of PP21 with PP28 (submicron filler from Nippon Kasei) brings about a reduction in mottle, which is already evident at a coverage of 0.5 g/m2, and also more rapid drying as seen by the strongly reduced penetration length in the results with the IGT Global Standard Tester 2. Replacement of P21 with PP02 (Sunsphere H33) also brings about a reduction in mottle, but less than with PP28.


Example 7
Combination of an Inorganic Porous Pigment and an Organic Polymeric Porous Pigment

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 10 with 0.04 g/m2 of the surfactant S07.














TABLE 10









Porous






pigment
Latex
Wt ratio
Binder
















cover-

cover-
porous

cover-




age

age
pigment

age


Example nr
nr
[g/m2]
nr
[g/m2]
to latex
nr
[g/m2]

















7/1
PP21
1.5
L04
2.0
0.75
B01
0.2


7/2
PP21
1.75
L04
2.0
1.0
B01
0.2


7/3
PP21
2.0
L04
2.0
1.0
B01
0.2


7/4
PP21
1.0
L04
2.0
0.75
B01
0.2



PP28
0.5


7/6
PP21
1.5
L04
2.0
0.875
B01
0.2



PP28
0.25


7/7
PP21
1.5
L04
2.0
1.0
B01
0.2



PP28
0.5


7/8
PP21
1.0
L04
2.0
0.75
B01
0.2



PP34
0.5


7/10
PP21
1.5
L04
2.0
0.875
B01
0.2



PP34
0.25


7/11
PP21
1.5
L04
2.0
1.0
B01
0.2



PP34
0.5


7/12
PP21
1.0
L04
2.0
0.75
B01
0.2



PP33
0.5


7/14
PP21
1.5
L04
2.0
0.875
B01
0.2



PP33
0.25


7/15
PP21
1.5
L04
2.0
1.0
B01
0.2



PP33
0.5


7/16
PP21
1.0
L04
2.0
0.75
B01
0.2



PP32
0.5


7/18
PP21
1.5
L04
2.0
0.875
B01
0.2



PP32
0.25


7/19
PP21
1.5
L04
2.0
1.0
B01
0.2



PP32
0.5









Printing tests were carried out on a Heidelberg GTO46 printing press with a K+E800 ink and as fountain 4% AGFA FS330 with 10% isopropanol and an IGT Global Standard Tester 2. The results are summarized in Table 11.













TABLE 11









Weight
Printing tests
IGT tests

















ratio


Dot
penetration

time to




porous


gain
test
penetration
avoid


Example
Porous
pigment
scratch

50%
length
test
set-off


nr
pigments
to latex
resistance
mottle
screen
[mm]
OD
[s]


















7/1
PP21
0.75
not OK
no
29
123.0
0.37
>58


7/2
PP21
1.0
not OK
no
29
106.0
0.50
24


7/3
PP21
1.0
not OK
no
28
90.0
0.60
9


7/4
PP21
0.75
OK
v. good
28
93.0
0.49
>58



PP28


7/6
PP21
0.875
not OK
v. good
29
97.0
0.51
31



PP28


7/7
PP21
1.0
not OK
v. good
28
83.0
0.61
24



PP28


7/8
PP21
0.75
OK
no
29
95.0
0.43
>58



PP34


7/10
PP21
0.875
not OK
no
28
92.0
0.50
39



PP34


7/11
PP21
1.0
not OK
v. good
28
82.0
0.55
24



PP34


7/12
PP21
0.75
OK
no
29
114.0
0.43
>58



PP33


7/14
PP21
0.875
OK
no
28
97.0
0.48
39



PP33


7/15
PP21
1.0
not OK
no
28
92.0
0.57
18



PP33


7/16
PP21
0.75
OK
no
30
114.0
0.42
>58



PP32


7/18
PP21
0.875
ca. OK
no
29
105.0
0.50
24



PP32


7/19
PP21
1.0
OK
no
28
99.0
0.52
18



PP32









There was no significant difference in dot gain or ink acceptance. Furthermore, no set-off was observed and there was no difference in ink adhesion. Moreover, the papers of EXAMPLES 7/4, 7/7, 7/8 and 7/14 gave very uniform ink layers. PP28 (Submicron filler from Nippon Kasei) and PP34 have a higher absorption speed than PP21 and PP28 (Submicron filler from Nippon Kasei) had the highest absorption capacity of the inorganic porous pigments evaluated.


Example 8
Combination of Porous and Opacifying Pigments

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 12 with Latex 04 with different combinations of porous and opacifying pigments.














TABLE 12









Porous pigment
Latex
Binder
Surfactants















Example

coverage

coverage

coverage

coverage


nr
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]





8/1
PP21
2.0
L04
2.2
B01
0.20
S07
0.01


FLX5010


8/2
PP21
1.5
L04
2.2
B01
0.20
S07
0.01


8/3
PP21
1.0
L04
2.0
B01
0.20
S07
0.01


8/4
PP21
0.5
L04
2.0
B01
0.20
S07
0.01


8/5


L04
2.2
B01
0.20
S07
0.01


8/6
PP21
1.5
L04
2.0
B01
0.20
S07
0.01



OP05
0.5


8/7
PP21
1.0
L04
2.2
B01
0.20
S07
0.01



OP05
1.0


8/8
PP21
0.5
L04
2.0
B01
0.20
S07
0.01



OP05
1.5


8/9
P05
2.0
L04
2.0
B01
0.20
S07
0.01


8/10
PP21
1.5
L04
2.2
B01
0.20
S07
0.01



OP10
0.5


8/11
PP21
1.0
L04
2.0
B01
0.20
S07
0.01



OP10
1.0


8/12
PP21
0.5
L04
2.2
B01
0.20
S07
0.01



OP10
1.5


8/13
OP10
2.0
L04
2.0
B01
0.20
S07
0.01


8/14
PP21
1.5
L04
2.0
B01
0.20
S07
0.01



PP25
0.5


8/15
PP21
1.0
L04
2.2
B01
0.20
S07
0.01



PP25
1.0


8/16
PP21
0.5
L04
2.0
B01
0.20
S07
0.01



PP25
1.5


8/17
PP25
2.0
L04
2.2
B01
0.20
S07
0.01


8/18
PP21
1.5
L04
2.0
B01
0.20
S07
0.01



OP09
0.5


8/19
PP21
1.0
L04
2.0
B01
0.20
S07
0.01



OP09
1.0


8/20
PP21
0.5
L04
2.2
B01
0.20
S07
0.01



OP09
1.5


8/21
OP09
2.0
L04
2.0
B01
0.20
S07
0.01


8/22
PP21
1.5
L04
2.2
B01
0.20
S07
0.01



PP26
0.5


8/23
PP21
1.0
L04
2.0
B01
0.20
S07
0.01



PP26
1.0


8/24
PP21
0.5
L04
2.0
B01
0.20
S07
0.01



PP26
1.5


8/25
PP26
2.0
L04
2.2
B01
0.20
S07
0.01









These papers were then subjected to printing tests using a Heidelberg GTO46 printing press with a K+E 123w ink and a fountain of 4% AGFA FS330 with 10% isopropanol. The resulting prints were evaluated on the basis of tape tests, powder tests, dot-gain evaluated with a Gretag Spectroeye densitometer, print mottle and scratch resistance with the results being given in Table 13 below.

















TABLE 13















IGT test




Tape
Dot



time to



Pigment
test
gain
Surface


avoid















Example

coverage
dry
50%
energy
print
Set-
set-off


nr.
nr
[g/m2]
[10 min]
screen
[mN/m]
mottle
off
[s]


















8/1
PP21
2.0

31
<36
no
no
9


FLX5010


8/2
PP21
1.5

33
<36
no
no
48


8/3
PP21
1.0

36
<36
yes
no
>58


8/4
PP21
0.5

36
38-40
strong
strong
>>58


8/5



29
36
strong
moderate


8/6
PP21
1.5

33
36
yes
no



OP05
0.5


8/7
PP21
1.0

35
42
strong
no



OP05
1.0


8/8
PP21
0.5

36
36
strong
no



OP05
1.5


8/9
OP05
2.0

37
42
strong
no


8/10
PP21
1.5

34
<36
moderate
no



OP10
0.5


8/11
PP21
1.0

36
<36
yes
no



OP10
1.0


8/12
PP21
0.5

38
36
strong
yes



OP10
1.5


8/13
OP10
2.0

15
<<36
v.
v.








strong
strong


8/14
PP21
1.5

32
<36
no
no
24



PP25
0.5


8/15
PP21
1.0

34
<36
slight
no
>58



PP25
1.0


8/16
PP21
0.5

36
36
yes
no
>>58



PP25
1.5


8/17
PP25
2.0

33
<36
strong
yes
>>58


8/18
PP21
1.5

33
<36
yes
no



OP09
0.5


8/19
PP21
1.0

34
36
strong
no



OP09
1.0


8/20
PP21
0.5

36
42
strong
strong



OP09
1.5


8/21
OP09
2.0

39
36
v.
v.








strong
strong


8/22
PP21
1.5

31
<36
slight
no
>58



PP26
0.5


8/23
PP21
1.0

32
38
yes
no
>>58



PP26
1.0


8/24
PP21
0.5

34
36
strong
no
>>58



PP26
1.5


8/25
PP26
2.0

32
36
strong
no
>>58









Decreasing the PP21-content increase mottle and dot gain with at PP21-contents below 1 g/m2 poor drying, set-off and poor ink adhesion.


Replacement of PP21 with OP05 (Jetcoat 30, CaCO3) resulted in a strong increase in print mottle and poorer ink adhesion, although Jetcoat 30 provides a contribution to the ink-drying process, allbeit small.


Replacement of PP21 with OP10 (Hydragloss 90, china clay/kaolin) resulted in a strong increase in print mottle and poorer ink adhesion. Moreover, OP10 provided no contribution to the ink-drying process.


Replacement of PP21 with PP25 [Micral 9400, [Al(OH)3] resulted in an improvement in ink adhesion and a slight increase in mottle. Moreover, PP25 contributed to the drying process, although less strongly than PP21 as shown by the complete replacement of PP21 with PP25 resulting in poor drying and strong mottle.


Replacement of PP21 with OP09 (Snowtex ST40, colloidal silica) resulted in a strong increase in print mottle and poorer ink adhesion. Moreover, OP09 provided no contribution to the ink-drying process.


Replacement of PP21 with PP26 (Digitex 1000, kaolin) had no effect on the mottle and improved the drying and ink adhesion.


Example 9
Screening of Different Water-Soluble Binders

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 14 with Latex 03 and Latex 04 with different binders to investigate whether this might reduce the print mottle.














TABLE 14









Porous pigment
Latex
Binder
Surfactants















Example

coverage

coverage

coverage

coverage


nr
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]





9/1
PP21
2.2
L03
2.2


S07
0.01


Dispercoll


U53


9/2
PP21
2.0
L03
2.0


S07
0.01


9/3
PP21
2.2
L03
2.2
B01
0.22
S07
0.01


9/4
PP21
2.0
L03
2.0
B01
0.20
S07
0.01


9/5
PP21
2.0
L03
2.0
B01
0.20
S07
0.01


9/6
PP21
2.2
L03
2.2
B02
0.22
S07
0.01


9/7
PP21
2.0
L03
2.0
B02
0.60
S07
0.01


9/8
PP21
2.2
L03
2.2
B03
0.22
S07
0.01


9/9
PP21
2.2
L03
2.2
B04
0.22
S07
0.01


9/10
PP21
2.0
L03
2.0
B01
0.20
S07
0.01







IN02
0.20


9/11
PP21
2.2
L04
2.2


S07
0.01


FLX5010


9/12
PP21
2.2
L04
2.2
B01
0.22
S07
0.01


9/13
PP21
2.2
L04
2.2
B01
0.22
S07
0.01


9/14
PP21
2.2
L04
2.2
B02
0.22
S07
0.01


9/15
PP21
2.2
L04
2.2
B02
0.22
S07
0.01


9/16
PP21
2.2
L04
2.2
B02
0.33
S07
0.01


9/17
PP21
2.2
L04
2.2
B02
0.44
S07
0.01


9/18
PP21
2.2
L04
2.2
B02
0.50
S07
0.01


9/19
PP21
2.2
L04
2.2
B03
0.22
S07
0.01


9/20
PP21
2.2
L04
2.2
B04
0.22
S07
0.01









These papers were then subjected to printing tests using a Heidelberg GTO46 printing press with a K+E 123w ink and a fountain of 4% Emerald Premium with 10% isopropanol. The resulting prints were evaluated on the basis of tape tests, powder tests, dot-gain evaluated with a Gretag Spectroeye densitometer, print mottle and scratch resistance with the results being given in Table 15 below.














TABLE 15









Binder

Dot gain















Example

coverage
Tape test
Powder
50%
print
Scratch


nr.
nr
[g/m2]
dry 10 min
test
screen
mottle
resistance





9/1


strong
OK
20
no
OK


Dispercoll


cohesive


U53


break


9/2


strong
OK

yes
OK





cohesive





break


9/3
B01
0.22
strong
light
22
no
OK





cohesive





break


9/4
B01
0.20
OK
powdery
33
no
OK


9/5
B01
0.20
light
powdery

no
OK





cohesive





break


9/6
B02
0.22
strong
light
20
yes
OK





cohesive





break


9/7
B02
0.20
strong
OK
31
no
OK





cohesive





break


9/8
B03
0.22
strong
OK
22
no
OK





cohesive





break


9/9
B04
0.22
strong
OK
22
no
OK





cohesive





break


9/10
B01
0.20
OK
OK

slight
OK



IN02
0.20


FLX5010


light
light
23
no
OK


9/11


cohesive





break


9/12
B01
0.22
OK
OK
19
no
OK


9/13
B01
0.22


26
no
OK


9/14
B02
0.22
strong
OK
23
yes
OK





cohesive





break


9/15
B02
0.22


27
no
OK


9/16
B02
0.33


27
no
OK


9/17
B02
0.44


28
no
OK


9/18
B02
0.50


28
no
OK


9/19
B03
0.22
OK
OK
24
no
OK


9/20
B04
0.22
OK
OK
24
no
OK









Surprisingly it was found that the papers with L03 as latex exhibited strong cohesive fracture in the receiving layer, whether or not a binder was used except when a combination of B01 and IN02 was used. The papers with L04 as latex only exhibited strong cohesive fracture when a polyvinyl alcohol with a low degree of hydrolysis, e.g. 74%, was used as a binder and the use polyvinyl alcohol with a degree of hydrolysis of at least 87-88% improved the resistance of the receiving layer to cohesive fracture. Increasing the concentration of B02 was not possible due to foaming and high viscosities.


Example 10
Printing Performance with Added Binder and/or Hardeners

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 16 including a binder to improve reduce the print mottle.















TABLE 16









Porous


matting




pigment
Latex
Binder
agent
Surfactants

















Example

coverage

coverage

coverage

coverage

coverage


nr
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]





10/1
PP21
2.0
L01
2.0
B01
0.2
MA01
0.06
S05
0.02


FLX5000








S06
0.04


10/2
PP21
3.0
L01
3.0
B01
0.3
MA01
0.06
S05
0.02


FLX5000








S06
0.04


10/3
PP21
2.0
L01
2.0
B01
0.2
MA01
0.06
S05
0.02


FLX5000








S06
0.04


10/4
PP21
2.0
L01
2.0
B01
0.2
MA01
0.06
S05
0.02


FLX5000








S06
0.04


10/5
PP21
2.0
L03
2.0
B01
0.2
MA01
0.06
S05
0.02


Dispercoll








S06
0.04


U53


10/6
PP21
2.0
L01
2.0
B01
0.2
MA01
0.06
S05
0.02


FLX5000








S06
0.04









These papers were then subjected to printing tests using an A.B. Dick 9860 with a K+E 123w ink and a fountain of 4% Emerald Premium in isopropanol. During the printing first the quantity of fountain was varied for a constant quantity of ink and then the quantity of fountain was kept constant and the quantity of ink varied. The resulting prints were evaluated on the basis of solid optical densities and dot gain with a Gretag Spectroeye densitometer with the results being given in Table 17. Furthermore, print penetration and drying time tests were carried out on the papers with an IGT Global Standard Tester 2, with the results also being given in Table 17.











TABLE 17









Example nr














10/1
10/2
10/3
10/4
10/5
10/6










Fountain environment













optimum
45%
45% Dg
45% Dg
45% Dg
45%
45% Dg



Dg



Dg


window below
10%
10%
10%
 5%
10%
10%


window above
20%
15%
15%
15%
30%
30%







Ink environment













optimum ink setting
10
10
10

8



window below
0
0
0

4


window above
10
5
5

8







dot gain for 50% screen at optimum setting













Gretag Spectroeye
26%
23%
24%
25%
22%
28%


mottle
slight
slight
v. slight
v. slight
no
v. slight







print penetration test with IGT Global Standard Tester 2













length of ink streak
89.3
90.7
90.3
91.3
89.0
90.3


on rotating drum


[mm]


optical density
0.59
0.67
0.56
0.57
0.49
0.56







set-off test with Huber set-off ink with IGT Global Standard Tester 2













drying time [s]
8
>11
>11
7
5
5









Using the paper of EXAMPLE 10/1 as a reference, the paper of EXAMPLE 10/2 with an increased layer thickness gave a marginally improved set-off performance and significantly reduced dot gain. The paper of EXAMPLE 10/3 with Zonyl FS0100, S07, as a surfactant rather than a mixture of surfactants exhibited similar set-off properties, but exhibited significantly reduced dot gain. However, the paper of EXAMPLE 10/4 with double the quantity of surfactant S07 resulted in a further reduction in dot gain, but at the expense of coating defects. Adding the silica and binder together, as in the paper of EXAMPLE 10/6, had no effect on the printing performance.


A comparison of the printing performance of the paper of EXAMPLE 10/5 with that of EXAMPLE 10/1 shows that the change in the latex from Latex 01 to Latex 03 resulted in a significant improvement: a reduction in set-off, i.e. in drying speed together with a significant reduction in dot gain.


Example 11

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 18 including a binder to improve reduce the print mottle.














TABLE 18









Porous pigment
Latex
Binder
Surfactant















Example

coverage

coverage

coverage

coverage


nr
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]





11/1
PP21
2.6
L04
2.6
B01
0.26
S07
0.01


FLX5010


11/2
PP21
3.0
L04
3.0
B01
0.30
S07
0.01


FLX5010


11/3
PP21
4.0
L04
4.0
B01
0.40
S07
0.01


FLX5010


11/4
PP21
2.0
L04
2.0
B01
0.20
S07
0.01


FLX5010


11/5
PP21
2.6
L03
2.6
B01
0.26
S07
0.01


Dispercoll


U53


11/6
PP21
3.0
L03
3.0
B01
0.30
S07
0.01


Dispercoll


U53


11/7
PP21
4.0
L03
4.0

0.40
S07
0.01


Dispercoll


U53


11/8
PP21
2.0
L03
2.0

0.20
S07
0.01


Dispercoll


U53









Print penetration tests were carried out on the papers of EXAMPLES 11/1 to 11/8 with an IGT Global Standard Tester 2, with the results also being given in Table 19.











TABLE 19









Example nr
















11/1
11/2
11/3
11/4
11/5
11/6
11/7
11/8











print penetration test with IGT Global Standard Tester 2















length of ink streak
109.7
113.3
89.7
100.3
83.3
88
81
85.7


on rotating drum [mm]


optical density
0.54
0.51
0.66
0.55
0.60
0.69
0.80
0.53









The results in Table xx clearly show the more rapid penetration of ink into layers containing Latex 03, Dispercoll U53, compared to comparable layers containing Latex 04, JONCRYL FLX5010.


Example 12
Evaluation of Matting Agents

The non-transparent microvoided biaxially stretched self-supporting films 1/LS1/BS1 coated with subbing layer 3 was coated with the compositions in Table 20 including different matting agents to improve the transport properties of the papers.















TABLE 20









Porous


matting




pigment
Latex
Binder
agent
Surfactants

















Example

coverage

coverage

coverage

coverage

coverage


nr
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]
nr
[g/m2]





12/1
PP21
2.2
L04
2.2
B01
0.22


S07
0.01


FLX5010


12/2
PP21
2.2
L04
2.2
B01
0.22


S07
0.01


12/3
PP21
2.2
L04
2.2
B01
0.22


S07
0.01


12/4
PP21
2.2
L04
2.2
B01
0.22
MA01
0.05
S07
0.01


12/5
PP21
2.2
L04
2.2
B01
0.22
MA01
0.1
S07
0.01


12/6
PP21
2.2
L04
2.2
B01
0.22
MA01
0.1
S07
0.01


12/7
PP21
2.2
L04
2.2
B01
0.22
MA01
0.1
S07
0.01


12/8
PP21
2.2
L04
2.2
B01
0.22
MA01
0.1
S07
0.01


12/9
PP21
2.2
L04
2.2
B01
0.22
MA01
0.15
S07
0.01


12/10
PP21
2.2
L04
2.2
B01
0.22
MA01
0.20
S07
0.01


12/11
PP21
2.2
L04
2.2
B01
0.22
MA01
0.25
S07
0.01


12/12
PP21
2.2
L04
2.2
B01
0.22
MA01
0.25
S07
0.01


12/13
PP21
2.2
L04
2.2
B01
0.22
MA01
0.30
S07
0.01


12/14
PP21
2.2
L04
2.2
B01
0.22
MA01
0.5
S07
0.01


12/15
PP21
2.2
L04
2.2
B01
0.22
MA02
0.1
S07
0.01


12/16
PP21
2.2
L04
2.2
B01
0.22
MA03
0.1
S07
0.01


12/17
PP21
2.2
L04
2.2
B01
0.22
MA04
0.1
S07
0.01


12/18
PP21
2.2
L04
2.2
B01
0.22
MA05
0.1
S07
0.01


12/19
PP21
2.2
L04
2.2
B01
0.22
MA06
0.1
S07
0.01


12/20
PP21
2.2
L04
2.2
B01
0.22
MA07
0.1
S07
0.01


12/21
PP21
2.2
L04
2.2
B01
0.22
MA08
0.1
S07
0.01


12/22
PP21
2.2
L04
2.2
B01
0.22
MA09
0.1
S07
0.01


12/23
PP21
2.2
L04
2.2
B01
0.22
MA10
0.04
S07
0.01


12/24
PP21
2.2
L04
2.2
B01
0.22
MA10
0.06
S07
0.01


12/25
PP21
2.2
L04
2.2
B01
0.22
MA10
0.08
S07
0.01


12/26
PP21
2.2
L04
2.2
B01
0.22
MA10
0.1
S07
0.01


12/27
PP21
2.2
L04
2.2
B01
0.22
MA10
0.1
S07
0.01


12/28
PP21
2.2
L04
2.2
B01
0.22
MA11
0.1
S07
0.01


12/29
PP21
2.2
L04
2.2
B01
0.22
MA12
0.04
S07
0.01


12/30
PP21
2.2
L04
2.2
B01
0.22
MA12
0.06
S07
0.01


12/31
PP21
2.2
L04
2.2
B01
0.22
MA12
0.08
S07
0.01


12/32
PP21
2.2
L04
2.2
B01
0.22
MA12
0.1
S07
0.01


12/33
PP21
2.2
L04
2.2
B01
0.22
MA12
0.1
S07
0.01









The papers were evaluated in a series of tests to establish the physical effect of the matting agents on the surface smoothness and the frictional coefficient between sheets. Surface roughness was determined by Bekk tests and Perth-O-meter measurements.


Furthermore the scratch resistance was evaluated qualitatively using a nail test and quantitatively using the Linimark evaluation method with a Roberta apparatus giving the threshold force at and above which scratching was observed. The results are summarized in Table 21 below.















TABLE 21









matting

Ra from





agent
Bekk
Pert-O-
Static
Scratch resistance tests















Example

coverage
test
meter
frictional
nail
Lini-mark
Lini-mark


nr
nr
[g/m2]
[sec]
[μm]
coefficient
test
wet [mN]
dry [mN]


















12/1


2285
0.36
0.76
OK




12/2


1205


ca.








OK


12/3


1701


ca.








OK


12/4
MA01
0.05
1175


ca.








OK


12/5
MA01
0.1
1407
0.34
0.61
OK


12/6
MA01
0.1
1147


ca.








OK


12/7
MA01
0.1
1406


ca.








OK


12/8
MA01
0.1
1737


OK
21
33


12/9
MA01
0.15
1108


ca.








OK


12/10
MA01
0.20
1187


ca.








OK


12/11
MA01
0.25
1025
0.50
0.61
OK


12/12
MA01
0.25
1061


ca.








OK


12/13
MA01
0.30
1009


ca.








OK


12/14
MA01
0.5
854
0.48
0.55
ca.








OK


12/15
MA02
0.1
409
0.37
0.69
v.








good


12/16
MA03
0.1
1153
0.33
0.78
not








OK


12/17
MA04
0.1
152.3
0.58
0.84
not








OK


12/18
MA05
0.1
423


ca.








OK


12/19
MA06
0.1
258


ca.








OK


12/20
MA07
0.1
685


ca,








OK


12/21
MA08
0.1
291


OK


12/22
MA09
0.1
566


OK


12/23
MA10
0.04
462


OK
15
20


12/24
MA10
0.06
392


OK
15
26


12/25
MA10
0.08
245


OK
17
29


12/26
MA10
0.1
491


OK


12/27
MA10
0.1
228


OK
19
34


12/28
MA11
0.1
816


ca.








OK


12/29
MA12
0.04
116


ca.








OK


12/30
MA12
0.06
61


ca.








OK


12/31
MA12
0.08
49


ca.








OK


12/32
MA12
0.1
170


OK


12/33
MA12
0.1
34


ca.








OK









The Bekk tests showed that a greater surface roughness was realized with matting agents MA02 and MA04 to MA12 than with MA01 or MA03, whereas according to the Pert-O-meter measurements papers with MA01 and MA04 exhibited higher R, values than with MA02 and MA03. The frictional measurements showed a significant reduction in friction with matting agents MA01 and MA02, whereas the paper of EXAMPLE 12/13 exhibited no significant change and the paper of EXAMPLE 12/14 showed an increase in frictional coefficients.


Printing evaluation was carried out using a Heidelberg GTO46 printing press with a K+E 123W ink and a fountain of 4% Emerald Premium with 10% isopropanol with an Azura printing plate exposed at 275 mJ/cm2 with a CREO exposure station. The printing results are summarized in Table 22 below.
















TABLE 22










Tape



IGT test



matting agent
test

dot gain

time to














Example

coverage
dry
Powder
for 50%
Print
avoid set-off


nr
nr
[g/m2]
[10 min]
test
screen
mottle
[s]

















12/1


OK
slight
27
no



12/2



OK

yes/no
9


12/3


OK
v. slight
24
yes/no


12/4
MA01
0.05

OK

no
24


12/5
MA01
0.1
OK
v. slight
26
no


12/6
MA01
0.1

OK

no
13


12/7
MA01
0.1
OK
v. slight
23
yes/no


12/8
MA01
0.1
OK
OK
28
no


12/9
MA01
0.15

OK

yes/no
18


12/10
MA01
0.20

OK

yes/no
18


12/11
MA01
0.25
OK
v. slight
26
no


12/12
MA01
0.25

OK

yes/no
18


12/13
MA01
0.30

OK

yes/no
18


12/14
MA01
0.5
OK
v. slight
27
no


12/15
MA02
0.1
OK
v. slight
29
no


12/16
MA03
0.1
OK
slight
31
no


12/17
MA04
0.1
OK
v. slight
26
no


12/18
MA05
0.1
OK
powdery
23
yes/no


12/19
MA06
0.1
OK
v. slight
23
yes/no


12/20
MA07
0.1
OK
v. slight
23
yes/no


12/21
MA08
0.1
OK
v. slight
23
yes/no


12/22
MA09
0.1
OK
powdery
23
yes/no


12/23
MA10
0.04
OK
OK
28
no


12/24
MA10
0.06
OK
OK
28
no


12/25
MA10
0.08
OK
OK
28
no


12/26
MA10
0.1
OK
v. good
23
yes/no


12/27
MA10
0.1
OK
OK
28
no


12/28
MA11
0.1
OK
powdery
23
yes/no


12/29
MA12
0.04
OK
OK
28
no


12/30
MA12
0.06
OK
OK
27
no


12/31
MA12
0.08
OK
OK
27
no


12/32
MA12
0.1
OK
v. slight
22
yes/no


12/33
MA12
0.1
OK
OK
27
no









An increase in dot gain was observed with papers with MA02 and MA03 and a slight reduction in the case of MA01 and MA04 to MA12. The scratch resistance of the papers was improved with the matting agents MA2 (polyethylene particles), MA8 (benzoguanine-melamine/formaldehyde particles), MA9 (polyamide particles) and MA 10 (ethylene-acrylic acid copolymer particles), was acceptable with the matting agent MA1, but deteriorated with matting agents MA3 and MA4.


Example 13
Printing Performance

The film 1/LS1/BS1 subbed with subbing layer 3 was coated with a single layer on both sides of the different receiving layer with the compositions and coating weights given in Table 23.
















TABLE 23











Slip agent/







Porous

matting


Coating


Example
Latex
pigment
Binder
agent
Surfactant
Proxel
wt



















nr
nr
wt %
nr
wt %
nr
wt %
nr
wt %
nr
wt %
wt %
[g/m2]






















13/1
L01
67.8
PP21
25.4


SL01
6.8



2.95


FLX5000


13/2
L01
67.5
PP21
25.3


SL01
6.8
S05
0.2

2.96


FLX5000








S06
0.1


13/3
L01
55.4
PP21
41.5


MA15
2.8
S05
0.2

3.61


FLX5000








S06
0.1


13/4
L04
47.58
PP21
47.48
B01
4.76


S07
0.18

4.84


FLX5010


13/5
L03
47.5
PP21
47.5
B01
4.8


S07
0.2

4.38


Dispercoll


U53


13/6
L04
46.62
PP21
46.51
B01
4.66
MA01
2.0
S07
0.17
0.004
4.94


FLX5010









A single layer with the composition of EXAMPLE 6 was also successfully coated on film 1/LS1/BS1 subbed with subbing layers 4 and 5. Furthermore, it could be coated on corona-treated PGA paper, corona-treated KLEPA paper and also on cast-coated paper.


The most significant differences in the papers of EXAMPLES 3 to 8 lie in the coating weight of the porous pigment PP21 rising from 0.75 g/m2 for the papers of EXAMPLES 3 and 4 to 1.5 g/m2 in the case of the paper of EXAMPLE 5 to 2.9 g/m2 in the case of the papers of EXAMPLES 6 and 7. This had a parallel effect on the drying behaviour of the papers, since the porosity of the receiving layers is determined by the quantity of porous pigment present therein, with the papers of EXAMPLES 3 and 4 exhibiting poor drying behaviour, whereas drying was acceptable in the case of the papers of EXAMPLES 5, 6 and 7. The scratch resistance of the papers of EXAMPLES 3, 4 and 5 was good, that of the paper of EXAMPLE 6 poor and those of the papers of EXAMPLES 7 and 8 made acceptable by the incorporation of a water-soluble binder to counter problems due to flaking.


The different latexes used had an influence upon the alkali resistance in which the paper of EXAMPLES 13/1, 13/2 and 13/3 with JONCRYL FLX5000 scored poorly, whereas the papers of EXAMPLES 13/4, 13/5 and 13/6 with JONCRYL FLX5010, also a styrene-acrylic latex and DISPERCOLL U53, a polyurethane resin scored well in this regard. However, DISPERCOLL U53 scored poorly in respect of UV-stability, whereas JONCRYL FLX 5000 and 5010 scored well in this regard.


The surface energies of the papers of EXAMPLES 13/3, 13/4, 13/5 and 13/6 were measured via contact angle measurements and the polar and disperse contributions determined. The results are summarized in Table 24.











TABLE 24









Surface free energy











Example nr
γSp mN/m
γSd mN/m
γS mN/m
liquids used














13/3
0.00
34.12
34.12
all liquids


13/4
0.79
41.92
42.71
only glycerine



2.59
42.46
45.06
all liquids


13/5
34.40
27.16
61.56
only glycerine


13/6
4.63
39.86
44.49
all liquids









These papers were then subjected to printing tests using a Heidelbery GT052 printing press equipped with a Dahlgren fountain system, which allowed the quantity of fountain by printing to be accurately set. During the printing first the quantity of fountain was varied for a constant quantity of ink and then the quantity of fountain was kept constant and the quantity of ink varied. The resulting prints were evaluated on the basis of solid optical densities and dot gain with a Gretag Spectroeye densitometer with the results being given in Table 25.











TABLE 25









Example nr














13/1
13/2
13/3
13/4
13/5
13/6










Fountain environment













optimum


50% Dg
55% Dg
50% Dg
60% Dg


window below


20%
25%
20%
25%


window above


5%
20%
25%
25%







Ink environment











optimum ink setting
8
8
8
8


window below
4
4
4
4


window above
2
6
6
10 







dot gain for 50% screen at optimum setting











Gretag Spectroeye
30%
19%
16%
16%









The papers of EXAMPLES 13/1 and 13/2 had an acceptable printing window, but set-off was a problem due to the poor drying performance of these papers. EXAMPLES 13/4 and 13/5 had clearly a greater printing window and less dot gain than the paper of EXAMPLE 13/3. Furthermore, the paper of EXAMPLE 5 exhibited print mottle, which was not observed with the papers of EXAMPLES 13/4 and 13/5. The papers of EXAMPLES 13/4 and 13/5 exhibited no set-off, rapid drying even at high ink settings, stable printing performance and exhibited identical printing behaviour to paper. No significant difference was observed between the printing performances of the papers of EXAMPLES 13/4 and 13/5.


Example 14
Optimalization of Receiving Layer Composition

The subbed film 1/LS1/BS1 was coated with a single layer on both sides of the different receiving layer compositions in Table 26.

















TABLE 26








wt










ratio


Total



latex

latex/
binder
Surfactact
coating
pore
oil


Example
L04
PP 12
porous
B01
S07
weight
volume*
absorption*


nr
[g/m2]
[g/m2]
pigment
[g/m2]
[g/m2]
[g/m2]
[mL/m2]
[mg/m2]























14/1
2
2
1.00
0.20
0.01

3.2
60


14/2
3
2
1.50
0.20
0.01

3.2
60


14/3
4
2
2.00
0.20
0.01

3.2
60


14/4
4
3
1.33
0.20
0.01

4.8
90


14/5
4
4
1.00
0.20
0.01

6.4
120


14/6
4
3
2.00
0.20
0.01

4.8
90


14/7
2
0.75
2.67
0.20
0.01

1.2
22.5


14/8
2
1
2.00
0.20
0.01

1.6
30


14/9
2
1.25
1.60
0.20
0.01

2
37.5


14/10
2
1.5
1.33
0.20
0.01

2.4
45


14/11
2
1.75
1.14
0.20
0.01

2.8
52.5


14/12
2
2
1.00
0.20
0.01

3.2
60


14/13
2.5
1.5
1.67
0.20
0.01

2.4
45


14/14
3
1.5
2.00
0.20
0.01

2.4
45


14/15
3.5
1.5
2.33
0.20
0.01

2.4
45


14/16
4
1.5
2.67
0.20
0.01

2.4
45


14/17
2
2
1.00
0.20
0.01
4.20
3.2
60


14/18
1.75
1.75
1.00
0.17
0.01
3.67
2.8
52.5


14/19
1.5
1.5
1.00
0.15
0.01
3.15
2.4
45


14/20
1.25
1.25
1.00
0.12
0.01
2.62
2
37.5


14/21
1
1
1.00
0.10
0.01
2.10
1.6
30


14/22
0.75
0.75
1.00
0.07
0.01
1.57
1.2
22.5


14/23
0.5
0.5
1.00
0.05
0.01
1.05
0.8
15


14/24
1.5
1.5
1.00
0.20
0.01
3.20
2.4
45


14/25
1.0
1.0
1.00
0.20
0.01
2.20
1.6
30


14/26
0.5
0.5
1.00
0.20
0.01
1.20
0.8
15





*calculated on the basis of the coverage of porous pigment from a pore volume of 1.6 mL/g and oil absorption of 300 g/100 g






These papers were then subjected to printing tests using a Heidelberg GT052 printing press with K+E 123w ink and a 4% Emerald Premium fountain with 10% isopropanol. This printing press was equipped with a Dahlgren fountain system, which allowed the quantity of fountain by printing to be accurately set.


The print quality was evaluated both by qualitative visual inspection tests and quantitative tests with an IGT Global Tester-2 in which the drying time to avoid set-off was determined according to ISO 3783 and ink penetration evaluated on the basis of the track formed and optical density of a 0.6 μL coloured dibutyl phthalate droplet applied to a paper with the receiving layer composition being evaluated on a rotating drum according to NEN 1836. The results are also given in Table 27.












TABLE 27










tests with IGT Global



visual inspection
Standard Tester-2











tests

time to














pore
oil

drying
ink penetration
avoid















Example
volume*
absorption*
print
set-
time
length

set-off


nr
[mL/m2]
[mg/cm2]
mottle
off
[hr]
[mm]
OD
[s]


















14/1
3.2
60
no







14/2
3.2
60
yes


14/3
3.2
60
yes


14/4
4.8
90
yes


14/5
6.4
120
no


14/6
4.8
90
yes


14/7
1.2
22.5
yes
yes


14/8
1.6
30
yes
yes


14/9
2
37.5
yes
no


14/10
2.4
45
yes
no


14/11
2.8
52.5
yes
no


14/12
3.2
60
no
no


14/13
2.4
45
yes
no


14/14
2.4
45
yes
slight


14/15
2.4
45
yes
yes


14/16
2.4
45
yes
yes


14/17
3.2
60
no
no

105.3
0.53
3


14/18
2.8
52.5
no
no

108.7
0.51
3


14/19
2.4
45
no
no

112.0
0.5
4


14/20
2
37.5
no
no

109.3
0.48
5


14/21
1.6
30
no
yes
>24
116.0
0.41
6


14/22
1.2
22.5
yes/no
yes
>24
126.3
0.36
>13


14/23
0.8
15
yes
yes
>120
143.0
0.29
>13


14/24
2.4
45
no
no

115.3
0.51
3


14/25
1.6
30
no
no

121.3
0.42
5


14/26
0.8
15
no
yes
>24
139.7
0.33
>13









The results in Table 27 clearly show for receiving layers based on Latex 04 and porous pigment PP21 that the combined requirements of avoiding print mottle and avoiding set-off with sufficiently rapid drying could only be realized with a ca. 1:1 weight ratio of Latex 04 to porous pigment PP21 together with a sufficient coverage of both ingredients i.e. sufficient porosity. These results clearly show that the required results were only realized at or above a theoretically available pore volume in the layer of 1.5 mL/m2. Print mottle is due to the solvent content of the printing ink being absorbed too slowly and set-off is due to the ink drying insufficiently quickly.


It has been surprisingly found that excellent printing behaviour can be obtained by practicing the various aspects of the present invention, these aspects including but not limited to coating a water-resistant support with a single layer with a layer thickness of at least 3 μm, a pore volume of at least 1.2 mL/m2 and which comprises at least one porous pigment.


The papers of the present invention provide, among other advantages, satisfactory printing under a wide range of printing conditions ensuring a constant printing quality over a long print run, e.g., variation in the quantity of ink, variation in the quantity of fountain in offset printing, with sufficiently fast drying to avoid offset of the image on following sheets (so-called ghost images) while ensuring that the ink is completely transferred to the paper during the printing process. These papers also exhibit acceptable whiteness, so not affect the colour of the print, exhibit acceptable opacity, are water-resistant, exhibit good scratch resistance, exhibit good chemical resistance to acids and alkali's and/or are suitable for outside applications, i.e., are resistant to UV-exposure and oxidation.


The present invention may include any feature or combination of features disclosed herein either implicitly or explicitly or any generalisation thereof. In view of the foregoing description it will be evident to a person skilled in the art that various modifications may be made within the scope of the invention.


Having described in detail preferred embodiments of the current invention, it will now be apparent to those skilled in the art that numerous modifications can be made therein without departing from the scope of the invention as defined in the following claims.


All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.


The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.


Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Of course, variations of those preferred embodiments will become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.

Claims
  • 1. A printable paper comprising a water-resistant support having two optionally subbed sides and a single layer on at least one of said optionally subbed sides, wherein said single layer has no substantial compositional variation, has a layer thickness of at least 3 μm, a pore volume of at least 1.2 mL/m2 and comprises at least one porous pigment, wherein said water-resistant support is a non-transparent microvoided axially stretched directly extruded linear polyester having dispersed therein from 5 to 20% by weight of at least one amorphous high polymer having a higher glass transition temperature than that of said linear polyester and from 0.1 to 10% by weight of at least one crystalline high polymer having a higher melting point than the glass transition temperature of said linear polyester, wherein said crystalline high polymer is isotactic poly(4-methyl-1-pentene), wherein said amorphous high polymer is selected from the group consisting of polystyrene, styrene copolymers, styrene-acrylonitrile-polymers, polyacrylates, acrylate-copolymers, polymethacrylates and methacrylate-copolymers.
  • 2. The printable paper according to claim 1, wherein said single layer further comprises at least one latex.
  • 3. The printable paper according to claim 2, wherein said at least one latex is an anionic acrylic latex or an aliphatic polyurethane latex.
  • 4. The printable paper according to claim 1, wherein said single layer further comprises at least one water-soluble binder.
  • 5. The printable paper according to claim 4, wherein said at least one water soluable binder is a hydrolyzed homo or copolymer of a vinylester.
  • 6. The printable paper according to claim 5, wherein said hydrolyzed homo or copolymer of a vinylester is a hydrolyzed homo or copolymer of vinyl acetate.
  • 7. The printable paper according to claim 2, wherein said single layer further comprises at least one insolubilizing agent unless said at least one latex is solubilized with ammonium hydroxide.
  • 8. The printable paper according to claim 7, wherein said insolubilizing agent is selected from the group consisting of: polyisocyanates, formaldehyde, formaldehyde derivatives, glutaraldehyde, glyoxal, glyoxal-derivatives, dimethylol urea, polyanionic metallic compounds and melamine-formaldehyde resins, and carboxylic acid anhydrides which contain a plurality of anhydride moieties on each molecular entity.
  • 9. The printable paper according to claim 1, wherein said single layer further comprises at least one hardened initially water-soluble polyhydroxy resin.
  • 10. The printable paper according to claim 1, wherein said water-resistant support is resin-coated cellulosic paper, a web having a fibrous structure formed with synthetic fibers or a web in which a film is directly extruded from a thermoplastic polymer.
  • 11. The printable paper according to claim 1, wherein said water-resistant support comprises at least 50% by weight of a linear polyester.
  • 12. The printable paper according to claim 1, wherein said styrene-acrylonitrile-polymer block copolymer.
  • 13. The printable paper according to claim 1, wherein said amorphous high polymer is styrene-acrylonitrile-block copolymer.
  • 14. The printable paper according to claim 13, wherein said single layer further comprises at least one latex.
  • 15. The printable paper according to claim 14, wherein said at least one latex is an anionic acrylic latex or an aliphatic polyurethane latex.
  • 16. The printable paper according to claim 13, wherein said single layer further comprises at least one water-soluble binder.
  • 17. A process for producing a printable paper according to claim 1 comprising the steps of: (i) optionally providing a water-resistant support having two sides with a subbing layer on at least one side; (ii) providing at least one side of said optionally subbed water-resistant support with a single layer having no substantial compositional variation, said single layer being applied to said optionally subbed water-resistant support as at least one wet aqueous layer in a single pass for each side of said water-resistant support, said at least one aqueous layer comprising at least one latex, at least one pigment, at least one binder and optionally at least one insolubilizing agent, wherein said latex is an anionic acrylic latex or an aliphatic polyurethane latex.
  • 18. The process according to claim 17, wherein said at least one pigment is a porous pigment or has a specific surface area greater than 100 m2/g.
  • 19. A process for utilizing a printable paper comprising: (a) providing a printable paper according to claim 1 and (b) subjecting the printable paper to a contact or contactless printing technique, technique.
  • 20. A process for utilizing a printable paper according to claim 1 comprising: (a) obtaining a printable paper by a process comprising the steps of: (i) optionally providing a water-resistant support having two sides with a subbing layer on at least one side; and (ii) providing at least one side of said optionally subbed water-resistant support with a single layer having no substantial compositional variation, said single layer being applied to said optionally subbed water-resistant support as at least one wet aqueous layer in a single pass for each side of said water-resistant support, said at least one aqueous layer comprising at least one latex, at least one pigment, at least one binder and optionally at least one insolubilizing agent, wherein said latex is an anionic acrylic latex or an aliphatic polyurethane latex, and (b) subjecting the printable paper to a contact or contactless printing technique.
Priority Claims (1)
Number Date Country Kind
08102728 Mar 2008 EP regional
CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 61/037,472 filed on Mar. 18, 2008, and the benefit of European Patent Application No. 08102728.6 filed on Mar. 18, 2008, each of which is incorporated by reference.

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Entry
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Related Publications (1)
Number Date Country
20090239057 A1 Sep 2009 US
Provisional Applications (1)
Number Date Country
61037472 Mar 2008 US