WO2017039585A1 - Primer compositions - Google Patents

Primer compositions Download PDF

Info

Publication number
WO2017039585A1
WO2017039585A1 PCT/US2015/047447 US2015047447W WO2017039585A1 WO 2017039585 A1 WO2017039585 A1 WO 2017039585A1 US 2015047447 W US2015047447 W US 2015047447W WO 2017039585 A1 WO2017039585 A1 WO 2017039585A1
Authority
WO
WIPO (PCT)
Prior art keywords
primer composition
primer
polyvinyl alcohol
starch nanoparticles
latex dispersion
Prior art date
Application number
PCT/US2015/047447
Other languages
French (fr)
Inventor
Bor-Jiunn Niu
Tao Chen
Original Assignee
Hewlett-Packard Development Company, L.P.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hewlett-Packard Development Company, L.P. filed Critical Hewlett-Packard Development Company, L.P.
Priority to EP15903176.4A priority Critical patent/EP3265318B1/en
Priority to US15/569,511 priority patent/US20180087222A1/en
Priority to CN201580080539.5A priority patent/CN107690499B/en
Priority to PCT/US2015/047447 priority patent/WO2017039585A1/en
Publication of WO2017039585A1 publication Critical patent/WO2017039585A1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/18Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising waxes
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/20Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/20Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H19/22Polyalkenes, e.g. polystyrene
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/36Coatings with pigments
    • D21H19/44Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
    • D21H19/54Starch
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/50Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
    • D21H21/52Additives of definite length or shape
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5218Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5227Macromolecular coatings characterised by organic non-macromolecular additives, e.g. UV-absorbers, plasticisers, surfactants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5236Macromolecular coatings characterised by the use of natural gums, of proteins, e.g. gelatins, or of macromolecular carbohydrates, e.g. cellulose
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5254Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers

Definitions

  • inkjet printing has become a popular way of recording images on various media surfaces, particularly paper. Some of these reasons include low printer noise, variable content recording, capability of high speed recording, and multi-color recording. Additionally, these advantages can be obtained at a relatively low price to consumers. Though there has been great improvement in inkjet printing, accompanying this improvement are increased demands by consumers in this area, e.g., higher speeds, higher resolution, full color image formation, increased stability, etc. Additionally, inkjet printing is becoming more prevalent in high speed commercial printing markets, competing with more laborious offset and gravure printing technologies.
  • Coated media typically used for these more conventional types of printing can perform somewhat acceptably on high speed inkjet printing devices, but these types of media are not always acceptable for inkjet technology as it relates to image quality, gloss, abrasion resistance, and other similar properties.
  • FIG. 1 illustrates a method of coating a media substrate in accordance with an example of the present technology
  • FIG. 2 shows a cross-sectional view of a coated media substrate in accordance with an example of the present technology
  • FIG. 3 shows a cross-sectional view of a coated media substrate in accordance with an example of the present technology.
  • the primer compositions can be ink-receiving primer compositions, in that the primer compositions can be used to form coatings for receiving inks such as inkjet inks.
  • the primer compositions can be applied to a substrate to form an ink-receiving layer on the substrate before printing inkjet ink over or onto the primer layer.
  • a primer composition can be applied to offset coated paper.
  • offset coated papers are significantly different from paper specifically designed for inkjet printing. Commercial offset paper often includes a smooth, nonporous surface coating that is difficult to penetrate by aqueous liquids.
  • offset coatings include inorganic pigments such as calcium carbonate and clay, as well as hydrophobic polymers that interact poorly with water-based inks.
  • Polymers used in offset media can also sometimes include latex binders, polystyrenes, polyolefins (polypropylene, polyethylene, polybutadiene), polyesters (PET), polyacrylates, polymethacrylates, poly (maleic anhydride), and/or others.
  • latex binders polystyrenes, polyolefins (polypropylene, polyethylene, polybutadiene), polyesters (PET), polyacrylates, polymethacrylates, poly (maleic anhydride), and/or others.
  • water-based inks printed on offset media often have poor image quality, dry very slowly (sometimes taking more than 24 hours), and have poor durability after drying.
  • the primer compositions described herein can be applied to a media substrate, such as an offset media substrate as described above, to improve the ability of the substrate to receive water-based inks.
  • a primer composition can be coated on a media substrate to improve the durability of images printed with water-based inks.
  • a media substrate that is normally less suitable for printing with water-based inks, such as offset media can be coated with the primer composition prior to printing. This coated media substrate can interact with water-based inks and provide a printed image with good durability after the ink dries on the coated media substrate.
  • the primer composition can include a water soluble polymeric binder, e.g., partially water soluble (at least 5%), mostly water soluble (at least 50%), or fully water soluble (at least 99%) in the primer composition.
  • Water soluble polymers can interact better with water-based inks compared to the hydrophobic coatings of offset media.
  • many types of water soluble polymeric binder exhibit poor dry smearfastness immediately after printing due to poor wet film strength.
  • starches, cellulose, polyethylene oxide, and polyvinylpyrrolidone (PVP) are examples of water soluble polymers that can have poor dry smearfastness when used in primers on offset media.
  • the primer composition can include polyvinyl alcohol as the water soluble polymeric binder.
  • the primer composition can include a cationic salt.
  • the hydroxyl groups of the polyvinyl alcohol can interact with the cationic salt to form a complex-like structure. This structure can result in enhanced wet film strength of the primer layer and the ink printed on top of the primer layer.
  • inkjet ink is printed on top of the primer, the ink can have improved instant dry
  • primer compositions including polyvinyl alcohols can provide desirable dry smearfastness, it is difficult to achieve both dry
  • mixtures of polyvinyl alcohol with common starch, polyvinyl pyrrolidone, or polyethylene oxide can in some cases provide good dry smearfastness or good wet smearfastness, but not both at the same time.
  • certain primer compositions including a mixture of polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion have been found to provide better dry smearfastness and wet smearfastness at the same time.
  • the primer composition can be used on offset paper in a
  • a more immediate or instant dry and wet smearfastness of the printed image can be such that no smearing occurs when the printed paper is rewound into a roll after printing. Because the printed image does not need extra time to dry before rewinding the paper, the press can run at a high speed in some examples.
  • a primer composition can include from 5 wt% to 70 wt%, based on the total weight of the primer composition, of a binder which includes a polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion.
  • the primer composition can also include a wax, a cationic salt, and water.
  • the primer composition can also include other additives such as surfactants. It is notable that when the water and other volatiles evaporate off, the weight percentage of the various solids in the composition increase, i.e. in the ink-receiving primer layer discussed hereinafter.
  • the polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion can act as a binder in the primer composition.
  • the amount of these ingredients can be sufficient to act as a binder to bind the remaining ingredients of the primer composition to the substrate.
  • the binder content of the primer composition can be within a range such that there is sufficient binder to bind the other ingredients of the primer to the substrate, but not so much that the ink-receiving properties of the primer are compromised.
  • too much binder can, in some cases, make the primer layer less porous and negatively impact the solution stability of the primer. This can interfere with the interaction between the primer layer and water-based inks.
  • the total amount of binder present in the primer composition can be from 5 wt% to 70 wt%. In other examples, the total amount of binder can be from 5 wt% to 50 wt%, 10 wt% to 30 wt%, or 10 wt% to 20 wt%.
  • the primer composition can include polyvinyl alcohol in an amount from 1 wt% to 40 wt%, 2 wt% to 30 wt%, or 5 wt% to 20 wt%, based on the weight of all dry components of the primer composition.
  • the type of polyvinyl alcohol is not particularly limited with respect to the molecular weight and degree of hydrolysis of the polyvinyl alcohol.
  • the polyvinyl alcohol can have a weight-average molecular weight from 1 ,000 M w to 300,000 M w . In further examples, the polyvinyl alcohol can have an average molecular weight from about 20,000 M w to about 250,000 M w . In more specific examples, the polyvinyl alcohol can have an average molecular weight from about 27,000 M w to about 205,000 M w .
  • the degree of hydrolysis of the polyvinyl alcohol can be from about 75 mol% to about 100 mol%. In certain examples, the degree of hydrolysis can be from about 86 mol% to about 100 mol%.
  • hydroxyl groups on the polyvinyl alcohol can interact with the cationic salt in the primer composition to form a complex-like structure, which improves the instant smearfastness of printed images on a primer coated substrate.
  • Non-limiting examples of polyvinyl alcohols that can be used in the primer composition include Poval® 3-88 (Kuraray
  • the polyvinyl alcohol can in some cases be a mixture of two or more types of polyvinyl alcohol.
  • the total amount of the polyvinyl alcohols can be from 1 wt% to 40 wt%, 2 wt% to 30 wt%, 5 wt% to 20 wt%, based on the weight of all dry components of the primer composition.
  • the range relates to total concentrations of polyvinyl alcohol, whether there be one, two, three, etc., specific polyvinyl alcohol species present.
  • the primer in one example, the primer
  • composition can include a mixture of two types of polyvinyl alcohol having different molecular weights.
  • the binder can include starch nanoparticles.
  • Starch is a carbohydrate consisting of linear or branched polysaccharide chains. Starch is often available in granular form, with granules having an average diameter of 10 ⁇ to 100 ⁇ or larger.
  • Starch nanoparticles are different from this common form of starch in that the starch nanoparticles have a smaller, nano-sized average diameter. For example, starch nanoparticles can have an average diameter from 1 nm to 1 ⁇ .
  • the starch nanoparticles used in the binder for the present primer compositions can have an average diameter within this range of 1 nm to 1 ⁇ .
  • the starch nanoparticles can have an average diameter from 10 nm to 500 nm, 20 nm to 200 nm, or 50 nm to 150 nm.
  • suitable starch nanoparticles for use in the present primer compositions include Ecosphere® 2202D, 2260, 2330 and 2326 (EcoSynthetix Inc.)- These starch nanoparticles are cross-linked starch with a nanoparticle structure, and can yield better durability than traditional starches that are non-crosslinked polymers.
  • the primer composition can include starch nanoparticles in an amount from 1 wt% to 20 wt%, 1 wt% to 10 wt%, or 2 wt% to 5 wt% based on the weight of all dry components of the primer composition.
  • the primer composition can further include a polymer latex dispersion.
  • the polymer latex dispersion can include latex particles suspended in water or an aqueous system.
  • the latex particles can be present in an amount from about 10 wt% to about 70 wt% based on the weight of all dry components of the primer composition.
  • the latex particles can be present in an amount from 20 wt% to 60 wt% based on the weight of all dry components of the primer composition.
  • the primer composition can be predominantly (greater than 50 wt% by dry weight) made up of the latex particles, the polyvinyl alcohol, the starch nanoparticles, wax, and the cationic salt.
  • the polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax, and cationic salt can make up at least 80 wt% of all dry ingredients in the primer composition.
  • the latex particles can be used to improve the film strength of the primer layer.
  • the glass transition temperature (Tg) of the latex can be from 0°C to 100°C.
  • the latex polymer can be anionic, nonionic, or cationic. In some examples, the latex particles can be cationic latex particles.
  • the latex particles can be made of polymers and copolymers including acrylic polymers or copolymers, vinyl acetate polymers or copolymers, polyester polymers or copolymers, vinylidene chloride polymers or copolymers, butadiene polymers or copolymers, styrene-butadiene polymers or copolymers, acrylonitrile-butadiene polymers or copolymers.
  • the latex particles can include a vinyl acetate-based polymer, an acrylic polymer, a styrene polymer, a styrene-butadiene (SBR)-based polymer, a polyester-based polymer, a vinyl chloride-based polymer, an acid-based polymer, or the like.
  • the latex particles can be a polymer or a copolymer including acrylic polymers, vinyl-acrylic copolymers and acrylic-polyurethane copolymers.
  • the latex particles can be cationic acrylate latex.
  • the latex can be a vinyl acetate polymer.
  • the latex can be a SBR polymer.
  • the latex particles can have a weight average molecular weight (M w ) of 5,000 M w to 500,000 M w . In one example, the latex particles can range from 150,000 M w to 300,000 M w . In some examples, the average particle diameter of the latex particles can be from 10 nm to 1 ⁇ and, as other examples, from 10 nm to 500 nm, and in yet other examples, from 50 nm to 250 nm.
  • the particle size distribution of the latex is not particularly limited, and either latex having a broad particle size distribution or latex having a mono-dispersed particle size distribution may be used. It is also possible to use two or more kinds of polymer fine particles each having a mono-dispersed particle size distribution in combination
  • the primer composition can include additional binders.
  • additional binders include cellulose, polyethylene oxide, polyvinyl pyrrolidone, and others.
  • the additional binders can also be mixtures of two or more water soluble polymeric binders.
  • the additional binders can be present in a smaller amount than the combined polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion.
  • the combined polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion can make up at least 10 wt% by dry weight of all binders present in the primer composition.
  • the combined polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion can make up at least 80 wt% by dry weight of all binders present in the primer composition.
  • the primer composition can be substantially free of any binder other than the polyvinyl alcohol, starch
  • nanoparticles and polymer latex dispersion.
  • the primer composition can also include a wax.
  • the wax can act as a slip aid to contribute to abrasion resistance and coefficient of friction (COF) reduction.
  • Suitable waxes can include particles of a synthetic wax, natural wax, combinations of a synthetic wax and a natural wax, combinations of two or more different synthetic waxes, or combinations of two or more different natural waxes, for example.
  • the synthetic wax can include polyethylene, polypropylene, polybutadiene, polytetrafluoroethylene, polyvinylfluoride, polyvinyldiene fluoride, polychlorotrifluoroethylene,
  • perfluoroalkoxy polymer perfluoropolyether, polyurethane
  • the natural wax can include carnauba wax, paraffin wax, montan wax, candelilla wax, ouricury wax, sufarcane wax, retamo wax, or beeswax.
  • the wax can be a polyethylene wax, such as a high density polyethylene wax.
  • slip aids that can be used include Michemshield® 29235 (Michelman, Inc.), Ultralube® E846 (Keim-Additec Surface GmbH), and
  • a wax can be present in the primer composition at an amount of 1 wt% to 20 wt% of all dry ingredients in the primer composition. In other examples, the wax can be present in an amount of 5 wt% to 15 wt% of all dry ingredients in the primer composition
  • the primer composition can also include a cationic salt.
  • the cationic salt can be present in an amount sufficient to immobilize pigment colorants in the ink to be printed over the primer and to yield good image quality.
  • the primer composition can include the cationic salt in an amount from 10 wt% to 50 wt%, 1 0 wt% to 40 wt%, 15 wt% to 30 wt%, or 20 wt% to 30 wt% based on the weight of all dry components of the primer composition.
  • the cationic salt can include a metal cation.
  • the metal cation can be sodium, calcium, copper, nickel, magnesium, zinc, barium, iron, aluminum, chromium, or other metal.
  • the cationic salt can also include an anion.
  • the anion can be fluoride, chloride, iodide, bromide, nitrate, chlorate, acetate, or RCOO " where R is hydrogen or any low molecular weight hydrocarbon chain, e.g., C1 to C12.
  • the anion can be a carboxylate derived from a saturated aliphatic monocarboxylic acid having 1 to 6 carbon atoms or a carbocyclic monocarboxylic acid having 7 to 1 1 carbon atoms.
  • saturated aliphatic monocarboxylic acid having 1 to 6 carbon atoms may include formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, and/or hexanoic acid.
  • the cationic salt can be a polyvalent metal salt made up of a divalent or higher polyvalent metallic ion and an anion.
  • the cationic salt can include calcium chloride, calcium nitrate, magnesium nitrate, magnesium acetate, and/or zinc acetate.
  • the cationic salt can include calcium chloride or calcium nitrate (CaCI 2 or Ca(N03) 2 ).
  • the cationic salt can include calcium chloride (CaCI 2 ).
  • the cationic salt can also be a mixture of two or more different cationic salts.
  • the total amount of the mixture of cationic salts can be 10 wt% to 50 wt%, 10 wt% to 40 wt%, 15 wt% to 30 wt%, or 20 wt% to 30 wt% based on the weight of all dry components of the primer composition. Whatever range is considered, it is understood that the range relates to total concentrations of salts, whether there be one, two, three, etc., specific salt species present.
  • many coating compositions for inkjet printing include inorganic pigments to improve the absorption properties of the coating.
  • inorganic pigments can include, for example, clays such as kaolin clay or calcined clay, ground calcium carbonate, precipitated calcium carbonate, barium sulfate, titanium dioxide, silica, aluminum trihydrate, aluminum oxide, boehmite, or combinations thereof.
  • the present primer composition can be substantially devoid of inorganic pigments.
  • the primer composition can include an inorganic pigment.
  • the primer composition can include an inorganic pigment in an amount of about 5 wt% or less of all dry components of the primer composition.
  • the primer composition can include a relatively small amount of inorganic pigment, such as less than 5 wt%.
  • the primer composition can be acidic and can include an inorganic pigment that is compatible with acid, such as a clay.
  • the primer composition can also include other coating additives such as surfactants, rheology modifiers, defoamers, optical brighteners, biocides, pH controlling agents, dyes, and other additives for further enhancing the properties of the primer composition.
  • coating additives such as surfactants, rheology modifiers, defoamers, optical brighteners, biocides, pH controlling agents, dyes, and other additives for further enhancing the properties of the primer composition.
  • the total amount of such optional coating additives can be present, individually, in the range of 0.01 wt% to 5 wt% of all dry ingredients of the primer composition.
  • FIG. 1 provides an exemplary method of coating a media substrate 100.
  • the method includes applying 1 10 a primer composition to a media substrate, wherein the primer composition includes from 5 wt% to 70 wt% binder including polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion.
  • the primer composition further includes a wax, a cationic salt and water.
  • the primer composition used in the method can have any of the ingredients in the amounts described above with respect to the primer composition.
  • the method can include applying a primer composition that includes the polyvinyl alcohol in an amount from 1 wt% to 40 wt% of all dry ingredients in the primer composition, starch nanoparticles in an amount from 1 wt% to 20 wt%, and a polymer latex dispersion in an amount from 20 wt% to 70 wt% of all dry ingredients in the primer composition.
  • the method can include applying a primer composition in which polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax and cationic salt make up at least 80 wt% of all dry ingredients in the primer composition.
  • the method can include applying a primer composition that is substantially devoid of inorganic pigments.
  • the method can include applying a primer composition that includes an inorganic pigment in an amount of about 5 wt% or less of all dry components of the primer composition.
  • the composition can be applied to the substrate by any of a number of coating methods.
  • the substrate can be coated by spray coating, dip coating, cascade coating, roll coating, gravure coating, curtain coating, air knife coating, cast coating, Meyer rod coating, blade coating, film coating, metered size press coating, puddle size press coating, calender stack, and/or by using other known coating techniques.
  • the thickness selected for the coating layer can vary.
  • the primer composition can be applied at a dry coat weight from 0.1 gsm to 20 gsm. In another example, the primer composition can be applied to the substrate at a dry coat weight from 0.3 gsm to 10 gsm.
  • the primer composition can be applied to the substrate at a dry coat weight from 0.3 gsm to 5 gsm. In another example, the primer composition can be applied to the substrate at a dry coat weight from 0.3 gsm to 1 gsm.
  • the method of coating the media substrate can further include allowing a sufficient time for the primer layer to dry before printing ink on the primer layer.
  • the primer layer can be dried with infrared lamp, hot air and combination thereof.
  • the primer layer can retain from about 0.01 wt% to about 10 wt% water, based on the total weight of the coating, when the coating is dry enough to print on.
  • the coating can have from about 1 wt% to about 6 wt% water remaining when an image is printed on the coated substrate.
  • dry coat weight described herein refers to dry components, even if some water remains behind in the final formulation coating.
  • Ink can be printed on the primer layer. Printing can occur when the primer layer is partially dry or fully dry (i.e. dry to the touch but still may include some residual water).
  • the ink can be a water-based ink such as a water-based inkjet ink.
  • Inkjet inks generally include a colorant dispersed or dissolved in an ink vehicle.
  • liquid vehicle or “ink vehicle” refers to the liquid fluid in which a colorant is placed to form an ink. Ink vehicles are well known in the art, and a wide variety of ink vehicles may be used with the systems and methods of the present disclosure.
  • Such ink vehicles may include a mixture of a variety of different agents, including, surfactants, solvents, co-solvents, anti- kogation agents, buffers, biocides, sequestering agents, viscosity modifiers, surface-active agents, water, etc.
  • the liquid vehicle can carry solid additives such as polymers, latexes, UV curable materials, plasticizers, etc.
  • the colorant discussed herein can include a pigment and/or dye.
  • dye refers to compounds or molecules that impart color to an ink vehicle.
  • dye includes molecules and compounds that absorb electromagnetic radiation or certain wavelengths thereof.
  • dyes include those that fluoresce and those that absorb certain wavelengths of visible light. In most instances, dyes are water soluble.
  • pigment generally includes pigment colorants, magnetic particles, aluminas, silicas, and/or other ceramics, organo-metallics or other opaque particles.
  • the colorant can be a pigment.
  • additives may be employed to enhance the properties of the ink composition for specific applications.
  • these additives are those added to inhibit the growth of harmful microorganisms.
  • These additives may be biocides, fungicides, and other microbial agents, which are routinely used in ink formulations.
  • Suitable microbial agents include, but are not limited to, NUOSEPT® (Nudex, Inc.), UCARCIDETM (Union carbide Corp.), VANCIDE® (R.T. Vanderbilt
  • the present technology also extends to coated media substrates.
  • the media substrate can include a variety of types of base substrate, including paper media, nonporous media, swellable media, microporous media, photobase media, offset media, coated media, uncoated media, and other types of media including plastics, vinyl media, fabrics, woven substrate, etc.
  • the substrate can be a swellable media, a microporous media, or an offset media.
  • the primer composition according to the present technology can be especially useful for coating offset media, which typically has a very small pore diameter
  • a coated media substrate according to the present technology can include a media substrate and a primer layer coated on a surface of the media substrate.
  • the primer layer can include a binder having polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion.
  • the primer layer can also include a wax and a cationic salt.
  • FIG. 2 shows an example of a coated media substrate 200.
  • a base substrate 210 is coated with a primer layer 220.
  • ink jet ink 230 can be printed to form a printed image.
  • the image can have improved instant dry smearfastness after printing.
  • FIG. 3 shows another example of a coated media substrate 300.
  • the base substrate 310 has a primer layer 320 coated on both sides of the base substrate.
  • Ink jet ink 330 is used to print images one or on both sides of the coated substrate.
  • the coated media substrate can be used for double sided printing.
  • the base substrate can also include its own coating, such as the hydrophobic coating on offset paper.
  • Certain coatings (or pre-coatings) described herein can often already be present as part of a substrate, and these coatings are not the same as the primer layer primarily discussed in the context of the present disclosure.
  • Offset media or photobase for example, already include coatings on one or both side of a substrate material (and thus are considered to be part of the base substrate).
  • the primer compositions of the present disclosure are those which are overcoated with respect to the pre-applied coatings, or alternatively, to substrates that are not already pre-coated.
  • Such coatings i.e. the pre-coating and/or the primer compositions of the present disclosure, can be present on either one side of a media substrate or both.
  • the primer layer on the coated substrate can be formed by applying the primer compositions disclosed herein using any of the methods disclosed herein.
  • the primer layer can include any of the additional ingredients in any of the amounts disclosed for the primer compositions described herein.
  • the primer layer can include the polymer latex dispersion in an amount from 10 wt% to 70 wt% of all dry components of the primer layer.
  • polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax, and cationic salt can make up at least 80 wt% of all dry components of the primer layer.
  • a printing system can include an inkjet ink and a coated media substrate as described above.
  • the coated media substrate can include a media substrate and a primer layer coated on a surface of the media substrate.
  • the primer layer can include a polyvinyl alcohol, starch nanoparticles, a polymer latex dispersion, a wax and a cationic salt.
  • Substrate or “media substrate” includes any base material that can be coated in accordance with examples of the present disclosure, such as film base substrates, polymer substrates, conventional paper substrates, photobase substrates, offset media substrates, and the like. Further, pre-coated and film coated substrates can be considered a “substrate” that can be further coated in accordance with examples of the present disclosure.
  • Slip aid refers to materials that can be added to coating compositions herein to provide abrasion resistance to coatings of the present disclosure.
  • “Instant dry smearfastness” refers to the ability of a printed image to resist smearing when rubbed with a dry instrument such as a finger or a Rubber Eraser Tool, immediately after printing or within a short time of being printed.
  • the short time can be, for example, from 1 second to 30 seconds, from 1 second to 20 seconds, or from 5 seconds to 10 seconds.
  • the short time can be the time required for a printed image to travel from the inkjet printer to a rewinding roll.
  • a printed image on an HP T230 Web Press® takes from 5 seconds to 10 seconds to reach the rewinder after being printed.
  • “Instant wet smearfastness” refers to the ability of a printed image to resist smearing when rubbed with a wet instrument such as a wet finger immediately after printing or within a short time of being printed.
  • the short time can be, for example, from 1 second to 30 seconds, from 1 second to 20 seconds, or from 5 seconds to 10 seconds.
  • the short time can be the time required for a printed image to travel from the inkjet printer to a rewinding roll.
  • a printed image on an HP T230 Web Press® takes from 5 seconds to 10 seconds to reach the rewinder after being printed.
  • “Instant mechability” refers to the instant dry and wet smearfastness and the scratch resistance of a sample after printing, drying, and reaching the rewinding station.
  • presses such as the HP T230 Web Press® or the HP T350 Web Press® exhibit printing speeds that are commensurate of what is considered to be “high speed.”
  • the HP T350 Web Press® can print text and/or other images on media at a rate of 400 feet per minute. This capability would be considered high speed. In another example, and more generally, printing at 100 feet per minute would also be considered high speed.
  • a weight ratio range of about 1 wt% to about 20 wt% should be interpreted to include not only the explicitly recited limits of 1 wt% and about 20 wt%, but also to include individual weights such as 2 wt%, 1 1 wt%, 14 wt%, and sub-ranges such as 10 wt% to 20 wt%, 5 wt% to 15 wt%, etc.
  • PolyoxTM N750 polyethylene oxide
  • Ultralube® D-806 1 1 10 10 10 10 (polyethylene wax)
  • PolyoxTM N750 (polyethylene oxide) - - - - -
  • Ultralube® D-806 1 10 10 (polyethylene wax) Calcium Chloride 27 26 26 26
  • Example formulations 1 -9 were coated onto Sterling® Ultra Gloss (Verso Corporation), 60# paper with 2 g/m 2 (gsm) of dry coating weight. Samples were printed with an HP CM8060 M FP Edgeline printer, from Hewlett- Packard Co., Palo Alto, CA, USA (HP), using HP A50 pigment inks (i.e. aqueous inkjet ink for digital inkjet printing). The printing process used involved 2 passes and six dry spin conditions to mimic high-speed, digital, web press inkjet printing. Dry and wet smearfastness refer to the ability of the printed image to resist appearance degradation upon rubbing or smearing the image by dry or wet finger. For the dry and wet finger smearfastness tests, a dry or wet finger was placed against a printed area, pushed with force of about 50 g/in 2 , and drawn toward the tester. The finger was then released to check the tested area.
  • the visual ranking is based on a 1 to 5 scale, with 1 being the worst and 5 being the best. A ranking equal to or greater than 3 is considered good and acceptable. A ranking below 3 is considered poor and not acceptable.
  • Examples 1 -5 did not include starch nanoparticles. These examples did not provide sufficient wet finger smearfastness.
  • Example 6 included starch nanoparticles, but no polyvinyl alcohol. This example showed very poor dry finger smearfastness and wet finger smearfastness.
  • Examples 7-9 included both starch nanoparticles and polyvinyl alcohol (as well as latex particles).
  • Example 7 provided excellent wet finger smearfastness but marginal dry finger
  • Examples 8 and 9 both provided good dry finger smearfastness and wet finger smearfastness. Therefore, these examples show that, although neither starch nanoparticles nor polyvinyl alcohol can provide sufficient wet and dry smearfastness when used alone, the combination of these two binders, along with latex particles) unexpectedly provides good wet and dry smearfastness.

Abstract

The present disclosure is drawn to primer compositions which can include a binder including polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion. The primer competitions can also include a wax, a cationic salt, and water.

Description

PRIMER COMPOSITIONS
BACKGROUND
[0001 ]There are several reasons that inkjet printing has become a popular way of recording images on various media surfaces, particularly paper. Some of these reasons include low printer noise, variable content recording, capability of high speed recording, and multi-color recording. Additionally, these advantages can be obtained at a relatively low price to consumers. Though there has been great improvement in inkjet printing, accompanying this improvement are increased demands by consumers in this area, e.g., higher speeds, higher resolution, full color image formation, increased stability, etc. Additionally, inkjet printing is becoming more prevalent in high speed commercial printing markets, competing with more laborious offset and gravure printing technologies. Coated media typically used for these more conventional types of printing, e.g., offset or gravure printing, can perform somewhat acceptably on high speed inkjet printing devices, but these types of media are not always acceptable for inkjet technology as it relates to image quality, gloss, abrasion resistance, and other similar properties. BRIEF DESCRIPTION OF THE DRAWINGS
[0002] Additional features and advantages of the disclosure will be apparent from the detailed description which follows, taken in conjunction with the accompanying drawings, which together illustrate, by way of example, features of the present technology.
[0003] FIG. 1 illustrates a method of coating a media substrate in accordance with an example of the present technology; [0004] FIG. 2 shows a cross-sectional view of a coated media substrate in accordance with an example of the present technology; and
[0005] FIG. 3 shows a cross-sectional view of a coated media substrate in accordance with an example of the present technology.
[0006] Reference will now be made to several examples that are illustrated herein, and specific language will be used herein to describe the same. It will nevertheless be understood that no limitation of the scope of the disclosure is thereby intended. DETAILED DESCRIPTION
[0007] The present disclosure is drawn to primer compositions. In some examples, the primer compositions can be ink-receiving primer compositions, in that the primer compositions can be used to form coatings for receiving inks such as inkjet inks. The primer compositions can be applied to a substrate to form an ink-receiving layer on the substrate before printing inkjet ink over or onto the primer layer. In one example, a primer composition can be applied to offset coated paper. Typically, offset coated papers are significantly different from paper specifically designed for inkjet printing. Commercial offset paper often includes a smooth, nonporous surface coating that is difficult to penetrate by aqueous liquids. In many cases, offset coatings include inorganic pigments such as calcium carbonate and clay, as well as hydrophobic polymers that interact poorly with water-based inks. Polymers used in offset media can also sometimes include latex binders, polystyrenes, polyolefins (polypropylene, polyethylene, polybutadiene), polyesters (PET), polyacrylates, polymethacrylates, poly (maleic anhydride), and/or others. As a result of the hydrophobic and nonporous properties of offset media, water-based inks printed on offset media often have poor image quality, dry very slowly (sometimes taking more than 24 hours), and have poor durability after drying.
[0008] The primer compositions described herein can be applied to a media substrate, such as an offset media substrate as described above, to improve the ability of the substrate to receive water-based inks. For example, a primer composition can be coated on a media substrate to improve the durability of images printed with water-based inks. In one example, a media substrate that is normally less suitable for printing with water-based inks, such as offset media, can be coated with the primer composition prior to printing. This coated media substrate can interact with water-based inks and provide a printed image with good durability after the ink dries on the coated media substrate.
[0009] In further detail, the primer composition can include a water soluble polymeric binder, e.g., partially water soluble (at least 5%), mostly water soluble (at least 50%), or fully water soluble (at least 99%) in the primer composition. Water soluble polymers can interact better with water-based inks compared to the hydrophobic coatings of offset media. However, many types of water soluble polymeric binder exhibit poor dry smearfastness immediately after printing due to poor wet film strength. For example, starches, cellulose, polyethylene oxide, and polyvinylpyrrolidone (PVP) are examples of water soluble polymers that can have poor dry smearfastness when used in primers on offset media.
[0010] Poor dry smearfastness immediately after printing can be problematic because the printed image can be easily smeared if the image is rubbed or otherwise disturbed soon after printing. For example, when using an HP high speed Web Press®, the printing is a continuous process and the paper is rewound as a roll after printing. The image or text printed on the paper can be smeared when the paper is rewound if the dry durability is poor. Prior solutions to this problem have included reducing the printing speed, increasing drying temperature, or increasing the drying zone. Several disadvantages are associated with these solutions, however. For example, increasing the drying time requires reducing the production rate, which increases the cost or time cost of printing. Harsh drying conditions can cause increased paper cockle. Increasing the size of the drying zone makes the printing system occupy a larger space, which increases the total cost or space cost of printing.
[0011 ] Surprisingly, certain primer compositions including polyvinyl alcohols and other components have been found to provide much better dry smearfastness immediately after printing. Thus, the primer composition can include polyvinyl alcohol as the water soluble polymeric binder. In addition to the polyvinyl alcohol, the primer composition can include a cationic salt. Thus, the hydroxyl groups of the polyvinyl alcohol can interact with the cationic salt to form a complex-like structure. This structure can result in enhanced wet film strength of the primer layer and the ink printed on top of the primer layer. When inkjet ink is printed on top of the primer, the ink can have improved instant dry
smearfastness.
[0012]Although primer compositions including polyvinyl alcohols can provide desirable dry smearfastness, it is difficult to achieve both dry
smearfastness and wet smearfastness at the same time. Poor wet smearfastness can cause poor mechability because the printed substrate can often be rewound before the primer layer and image are completely dry. Mixtures of different water soluble polymeric binders can be used to adjust the dry smearfastness and wet smearfastness of the primer composition. However, many mixtures of water soluble polymeric binders are unable to provide both good dry smearfastness and good wet smearfastness. For example, mixtures of polyvinyl alcohol with common starch, polyvinyl pyrrolidone, or polyethylene oxide can in some cases provide good dry smearfastness or good wet smearfastness, but not both at the same time. However, certain primer compositions including a mixture of polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion have been found to provide better dry smearfastness and wet smearfastness at the same time.
[0013] The primer composition can be used on offset paper in a
continuous printing system such as the HP high speed Web Press® mentioned above. In some cases, a more immediate or instant dry and wet smearfastness of the printed image can be such that no smearing occurs when the printed paper is rewound into a roll after printing. Because the printed image does not need extra time to dry before rewinding the paper, the press can run at a high speed in some examples. These advantages can be obtained without compromising print quality.
[0014] With this description in mind, in some examples, the present technology provides primer compositions. In one example, a primer composition can include from 5 wt% to 70 wt%, based on the total weight of the primer composition, of a binder which includes a polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion. The primer composition can also include a wax, a cationic salt, and water. In some examples, the primer composition can also include other additives such as surfactants. It is notable that when the water and other volatiles evaporate off, the weight percentage of the various solids in the composition increase, i.e. in the ink-receiving primer layer discussed hereinafter.
[0015] The polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion can act as a binder in the primer composition. Generally, the amount of these ingredients can be sufficient to act as a binder to bind the remaining ingredients of the primer composition to the substrate. In some examples, the binder content of the primer composition can be within a range such that there is sufficient binder to bind the other ingredients of the primer to the substrate, but not so much that the ink-receiving properties of the primer are compromised. As an example, too much binder can, in some cases, make the primer layer less porous and negatively impact the solution stability of the primer. This can interfere with the interaction between the primer layer and water-based inks. In some examples, the total amount of binder present in the primer composition can be from 5 wt% to 70 wt%. In other examples, the total amount of binder can be from 5 wt% to 50 wt%, 10 wt% to 30 wt%, or 10 wt% to 20 wt%.
[0016] In further detail, the primer composition can include polyvinyl alcohol in an amount from 1 wt% to 40 wt%, 2 wt% to 30 wt%, or 5 wt% to 20 wt%, based on the weight of all dry components of the primer composition.
[0017] The type of polyvinyl alcohol is not particularly limited with respect to the molecular weight and degree of hydrolysis of the polyvinyl alcohol.
However, in some examples, the polyvinyl alcohol can have a weight-average molecular weight from 1 ,000 Mw to 300,000 Mw. In further examples, the polyvinyl alcohol can have an average molecular weight from about 20,000 Mw to about 250,000 Mw. In more specific examples, the polyvinyl alcohol can have an average molecular weight from about 27,000 Mw to about 205,000 Mw. The degree of hydrolysis of the polyvinyl alcohol can be from about 75 mol% to about 100 mol%. In certain examples, the degree of hydrolysis can be from about 86 mol% to about 100 mol%. It is believed that the hydroxyl groups on the polyvinyl alcohol can interact with the cationic salt in the primer composition to form a complex-like structure, which improves the instant smearfastness of printed images on a primer coated substrate. Non-limiting examples of polyvinyl alcohols that can be used in the primer composition include Poval® 3-88 (Kuraray
America, Inc.) (14,000 Mw, 86.7-88.7 mol% hydrolysis); Poval® 4-88 (Kuraray America, Inc.) (31 ,000 Mw, 86.7-88.7 mol% hydrolysis); Poval® 4-98 (Kuraray America, Inc.) (27,000 Mw, 98-98.8 mol% hydrolysis); Poval® 5-88 (Kuraray America, Inc.) (37,000 Mw, 86.7-88.7 mol% hydrolysis); Poval® 8-88 (Kuraray America, Inc.) (67,000 Mw, 86.7-88.7 mol% hydrolysis); Poval® 13-88 (Kuraray America, Inc.) (86.7-88.7 mol% hydrolysis); Poval® 18-88 (Kuraray America, Inc.) (130,000 Mw, 86.7-88.7 mol% hydrolysis); Poval® 23-88 (Kuraray America, Inc.) (150,000 Mw, 86.7-88.7 mol% hydrolysis); Poval® 26-88 (Kuraray America, Inc.) (160,000 Mw, 86.7-88.7 mol% hydrolysis); and Poval® 40-88 (Kuraray America, Inc.) (205,000 Mw, 86.7-88.7 mol% hydrolysis).
[0018] The polyvinyl alcohol can in some cases be a mixture of two or more types of polyvinyl alcohol. In such examples, the total amount of the polyvinyl alcohols can be from 1 wt% to 40 wt%, 2 wt% to 30 wt%, 5 wt% to 20 wt%, based on the weight of all dry components of the primer composition.
Whatever range is considered, it is understood that the range relates to total concentrations of polyvinyl alcohol, whether there be one, two, three, etc., specific polyvinyl alcohol species present. In one example, the primer
composition can include a mixture of two types of polyvinyl alcohol having different molecular weights.
[0019] In addition to the polyvinyl alcohol, the binder can include starch nanoparticles. Starch is a carbohydrate consisting of linear or branched polysaccharide chains. Starch is often available in granular form, with granules having an average diameter of 10 μιη to 100 μιη or larger. Starch nanoparticles are different from this common form of starch in that the starch nanoparticles have a smaller, nano-sized average diameter. For example, starch nanoparticles can have an average diameter from 1 nm to 1 μιη. The starch nanoparticles used in the binder for the present primer compositions can have an average diameter within this range of 1 nm to 1 μιη. In some examples, the starch nanoparticles can have an average diameter from 10 nm to 500 nm, 20 nm to 200 nm, or 50 nm to 150 nm. [0020] Non-limiting examples of suitable starch nanoparticles for use in the present primer compositions include Ecosphere® 2202D, 2260, 2330 and 2326 (EcoSynthetix Inc.)- These starch nanoparticles are cross-linked starch with a nanoparticle structure, and can yield better durability than traditional starches that are non-crosslinked polymers. In some examples, the primer composition can include starch nanoparticles in an amount from 1 wt% to 20 wt%, 1 wt% to 10 wt%, or 2 wt% to 5 wt% based on the weight of all dry components of the primer composition.
[0021 ] The primer composition can further include a polymer latex dispersion. The polymer latex dispersion can include latex particles suspended in water or an aqueous system. In some examples, the latex particles can be present in an amount from about 10 wt% to about 70 wt% based on the weight of all dry components of the primer composition. In further examples, the latex particles can be present in an amount from 20 wt% to 60 wt% based on the weight of all dry components of the primer composition. Additionally, the primer composition can be predominantly (greater than 50 wt% by dry weight) made up of the latex particles, the polyvinyl alcohol, the starch nanoparticles, wax, and the cationic salt. In one example, the polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax, and cationic salt, can make up at least 80 wt% of all dry ingredients in the primer composition.
[0022] The latex particles can be used to improve the film strength of the primer layer. In one example, the glass transition temperature (Tg) of the latex can be from 0°C to 100°C. The latex polymer can be anionic, nonionic, or cationic. In some examples, the latex particles can be cationic latex particles.
[0023] In other examples, the latex particles can be made of polymers and copolymers including acrylic polymers or copolymers, vinyl acetate polymers or copolymers, polyester polymers or copolymers, vinylidene chloride polymers or copolymers, butadiene polymers or copolymers, styrene-butadiene polymers or copolymers, acrylonitrile-butadiene polymers or copolymers. In another example, the latex particles can include a vinyl acetate-based polymer, an acrylic polymer, a styrene polymer, a styrene-butadiene (SBR)-based polymer, a polyester-based polymer, a vinyl chloride-based polymer, an acid-based polymer, or the like. In one aspect, the latex particles can be a polymer or a copolymer including acrylic polymers, vinyl-acrylic copolymers and acrylic-polyurethane copolymers. In another aspect, the latex particles can be cationic acrylate latex. In one specific aspect, the latex can be a vinyl acetate polymer. In another specific aspect, the latex can be a SBR polymer.
[0024] Generally, the latex particles can have a weight average molecular weight (Mw) of 5,000 Mw to 500,000 Mw. In one example, the latex particles can range from 150,000 Mw to 300,000 Mw. In some examples, the average particle diameter of the latex particles can be from 10 nm to 1 μιη and, as other examples, from 10 nm to 500 nm, and in yet other examples, from 50 nm to 250 nm. The particle size distribution of the latex is not particularly limited, and either latex having a broad particle size distribution or latex having a mono-dispersed particle size distribution may be used. It is also possible to use two or more kinds of polymer fine particles each having a mono-dispersed particle size distribution in combination
[0025] In some cases, the primer composition can include additional binders. Non-limiting examples of such binders include cellulose, polyethylene oxide, polyvinyl pyrrolidone, and others. The additional binders can also be mixtures of two or more water soluble polymeric binders. In some examples, if additional binders are present then the additional binders can be present in a smaller amount than the combined polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion. In further examples, the combined polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion can make up at least 10 wt% by dry weight of all binders present in the primer composition. In still further examples, the combined polyvinyl alcohol, starch nanoparticles, and polymer latex dispersion can make up at least 80 wt% by dry weight of all binders present in the primer composition. In a specific example, the primer composition can be substantially free of any binder other than the polyvinyl alcohol, starch
nanoparticles, and polymer latex dispersion.
[0026]The primer composition can also include a wax. In some examples, the wax can act as a slip aid to contribute to abrasion resistance and coefficient of friction (COF) reduction. Suitable waxes can include particles of a synthetic wax, natural wax, combinations of a synthetic wax and a natural wax, combinations of two or more different synthetic waxes, or combinations of two or more different natural waxes, for example. In some examples, the synthetic wax can include polyethylene, polypropylene, polybutadiene, polytetrafluoroethylene, polyvinylfluoride, polyvinyldiene fluoride, polychlorotrifluoroethylene,
perfluoroalkoxy polymer, perfluoropolyether, polyurethane,
polyethylenechlorotrifluoroethylene, polyethylene-vinyl acetate, epoxy resin, silicone resin, polyamide resin, polyamide, or polyester resin. In some examples, the natural wax can include carnauba wax, paraffin wax, montan wax, candelilla wax, ouricury wax, sufarcane wax, retamo wax, or beeswax. In one example, the wax can be a polyethylene wax, such as a high density polyethylene wax.
Commercially available slip aids that can be used include Michemshield® 29235 (Michelman, Inc.), Ultralube® E846 (Keim-Additec Surface GmbH), and
Ultralube® D-806 (Keim-Additec Surface GmbH), for example. In some examples, a wax can be present in the primer composition at an amount of 1 wt% to 20 wt% of all dry ingredients in the primer composition. In other examples, the wax can be present in an amount of 5 wt% to 15 wt% of all dry ingredients in the primer composition
[0027]The primer composition can also include a cationic salt. The cationic salt can be present in an amount sufficient to immobilize pigment colorants in the ink to be printed over the primer and to yield good image quality. In some examples, the primer composition can include the cationic salt in an amount from 10 wt% to 50 wt%, 1 0 wt% to 40 wt%, 15 wt% to 30 wt%, or 20 wt% to 30 wt% based on the weight of all dry components of the primer composition.
[0028] The cationic salt can include a metal cation. In some examples, the metal cation can be sodium, calcium, copper, nickel, magnesium, zinc, barium, iron, aluminum, chromium, or other metal. The cationic salt can also include an anion. In some examples, the anion can be fluoride, chloride, iodide, bromide, nitrate, chlorate, acetate, or RCOO" where R is hydrogen or any low molecular weight hydrocarbon chain, e.g., C1 to C12. In a more specific example, the anion can be a carboxylate derived from a saturated aliphatic monocarboxylic acid having 1 to 6 carbon atoms or a carbocyclic monocarboxylic acid having 7 to 1 1 carbon atoms. Examples of saturated aliphatic monocarboxylic acid having 1 to 6 carbon atoms may include formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, and/or hexanoic acid. In some cases, the cationic salt can be a polyvalent metal salt made up of a divalent or higher polyvalent metallic ion and an anion. In certain examples, the cationic salt can include calcium chloride, calcium nitrate, magnesium nitrate, magnesium acetate, and/or zinc acetate. In one aspect, the cationic salt can include calcium chloride or calcium nitrate (CaCI2 or Ca(N03)2). In one additional specific aspect, the cationic salt can include calcium chloride (CaCI2). The cationic salt can also be a mixture of two or more different cationic salts. In such examples, the total amount of the mixture of cationic salts can be 10 wt% to 50 wt%, 10 wt% to 40 wt%, 15 wt% to 30 wt%, or 20 wt% to 30 wt% based on the weight of all dry components of the primer composition. Whatever range is considered, it is understood that the range relates to total concentrations of salts, whether there be one, two, three, etc., specific salt species present.
[0029] Many coating compositions for inkjet printing include inorganic pigments to improve the absorption properties of the coating. Such inorganic pigments can include, for example, clays such as kaolin clay or calcined clay, ground calcium carbonate, precipitated calcium carbonate, barium sulfate, titanium dioxide, silica, aluminum trihydrate, aluminum oxide, boehmite, or combinations thereof. However, in some examples, the present primer composition can be substantially devoid of inorganic pigments. In other examples, the primer composition can include an inorganic pigment. In some examples, the primer composition can include an inorganic pigment in an amount of about 5 wt% or less of all dry components of the primer composition. Thus, the primer composition can include a relatively small amount of inorganic pigment, such as less than 5 wt%. In certain examples, the primer composition can be acidic and can include an inorganic pigment that is compatible with acid, such as a clay.
[0030]The primer composition can also include other coating additives such as surfactants, rheology modifiers, defoamers, optical brighteners, biocides, pH controlling agents, dyes, and other additives for further enhancing the properties of the primer composition. The total amount of such optional coating additives can be present, individually, in the range of 0.01 wt% to 5 wt% of all dry ingredients of the primer composition.
[0031 ] The present technology also extends to methods of coating a media substrate. FIG. 1 provides an exemplary method of coating a media substrate 100. The method includes applying 1 10 a primer composition to a media substrate, wherein the primer composition includes from 5 wt% to 70 wt% binder including polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion. The primer composition further includes a wax, a cationic salt and water.
[0032]The primer composition used in the method can have any of the ingredients in the amounts described above with respect to the primer composition. In a particular example, the method can include applying a primer composition that includes the polyvinyl alcohol in an amount from 1 wt% to 40 wt% of all dry ingredients in the primer composition, starch nanoparticles in an amount from 1 wt% to 20 wt%, and a polymer latex dispersion in an amount from 20 wt% to 70 wt% of all dry ingredients in the primer composition. In a further example, the method can include applying a primer composition in which polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax and cationic salt make up at least 80 wt% of all dry ingredients in the primer composition. In yet another example, the method can include applying a primer composition that is substantially devoid of inorganic pigments. In another example, the method can include applying a primer composition that includes an inorganic pigment in an amount of about 5 wt% or less of all dry components of the primer composition.
[0033] The composition can be applied to the substrate by any of a number of coating methods. In accordance with examples of the present disclosure, the substrate can be coated by spray coating, dip coating, cascade coating, roll coating, gravure coating, curtain coating, air knife coating, cast coating, Meyer rod coating, blade coating, film coating, metered size press coating, puddle size press coating, calender stack, and/or by using other known coating techniques. The thickness selected for the coating layer can vary. In one example, the primer composition can be applied at a dry coat weight from 0.1 gsm to 20 gsm. In another example, the primer composition can be applied to the substrate at a dry coat weight from 0.3 gsm to 10 gsm. In another example, the primer composition can be applied to the substrate at a dry coat weight from 0.3 gsm to 5 gsm. In another example, the primer composition can be applied to the substrate at a dry coat weight from 0.3 gsm to 1 gsm.
[0034]The method of coating the media substrate can further include allowing a sufficient time for the primer layer to dry before printing ink on the primer layer. The primer layer can be dried with infrared lamp, hot air and combination thereof. The primer layer can retain from about 0.01 wt% to about 10 wt% water, based on the total weight of the coating, when the coating is dry enough to print on. In some examples, the coating can have from about 1 wt% to about 6 wt% water remaining when an image is printed on the coated substrate. Thus, it is understood that the "dry coat weight" described herein refers to dry components, even if some water remains behind in the final formulation coating.
[0035] Ink can be printed on the primer layer. Printing can occur when the primer layer is partially dry or fully dry (i.e. dry to the touch but still may include some residual water). In some cases, the ink can be a water-based ink such as a water-based inkjet ink. Inkjet inks generally include a colorant dispersed or dissolved in an ink vehicle. As used herein, "liquid vehicle" or "ink vehicle" refers to the liquid fluid in which a colorant is placed to form an ink. Ink vehicles are well known in the art, and a wide variety of ink vehicles may be used with the systems and methods of the present disclosure. Such ink vehicles may include a mixture of a variety of different agents, including, surfactants, solvents, co-solvents, anti- kogation agents, buffers, biocides, sequestering agents, viscosity modifiers, surface-active agents, water, etc. Though not part of the liquid vehicle per se, in addition to the colorants, the liquid vehicle can carry solid additives such as polymers, latexes, UV curable materials, plasticizers, etc.
[0036] Generally the colorant discussed herein can include a pigment and/or dye. As used herein, "dye" refers to compounds or molecules that impart color to an ink vehicle. As such, dye includes molecules and compounds that absorb electromagnetic radiation or certain wavelengths thereof. For example, dyes include those that fluoresce and those that absorb certain wavelengths of visible light. In most instances, dyes are water soluble. Furthermore, as used herein, "pigment" generally includes pigment colorants, magnetic particles, aluminas, silicas, and/or other ceramics, organo-metallics or other opaque particles. In one example, the colorant can be a pigment.
[0037] Consistent with the formulation of this disclosure, various other additives may be employed to enhance the properties of the ink composition for specific applications. Examples of these additives are those added to inhibit the growth of harmful microorganisms. These additives may be biocides, fungicides, and other microbial agents, which are routinely used in ink formulations.
Examples of suitable microbial agents include, but are not limited to, NUOSEPT® (Nudex, Inc.), UCARCIDE™ (Union carbide Corp.), VANCIDE® (R.T. Vanderbilt
Co.), PROXEL® (ICI America), ACTICIDE® (Thor Specialties Inc.) and combinations thereof.
[0038] The present technology also extends to coated media substrates.
The media substrate can include a variety of types of base substrate, including paper media, nonporous media, swellable media, microporous media, photobase media, offset media, coated media, uncoated media, and other types of media including plastics, vinyl media, fabrics, woven substrate, etc. In certain examples, the substrate can be a swellable media, a microporous media, or an offset media.
The primer composition according to the present technology can be especially useful for coating offset media, which typically has a very small pore diameter
(often referred to a nonporous) and hydrophobic surface that does not interact well with water based inks.
[0039] In one example, a coated media substrate according to the present technology can include a media substrate and a primer layer coated on a surface of the media substrate. The primer layer can include a binder having polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion. The primer layer can also include a wax and a cationic salt.
[0040] FIG. 2 shows an example of a coated media substrate 200. A base substrate 210 is coated with a primer layer 220. On top of the primer layer, ink jet ink 230 can be printed to form a printed image. The image can have improved instant dry smearfastness after printing. [0041 ] FIG. 3 shows another example of a coated media substrate 300. In this example, the base substrate 310 has a primer layer 320 coated on both sides of the base substrate. Ink jet ink 330 is used to print images one or on both sides of the coated substrate. Thus, the coated media substrate can be used for double sided printing. Although not shown in the figures, the base substrate can also include its own coating, such as the hydrophobic coating on offset paper. Certain coatings (or pre-coatings) described herein can often already be present as part of a substrate, and these coatings are not the same as the primer layer primarily discussed in the context of the present disclosure. Offset media or photobase, for example, already include coatings on one or both side of a substrate material (and thus are considered to be part of the base substrate). The primer compositions of the present disclosure, conversely, are those which are overcoated with respect to the pre-applied coatings, or alternatively, to substrates that are not already pre-coated. Such coatings, i.e. the pre-coating and/or the primer compositions of the present disclosure, can be present on either one side of a media substrate or both.
[0042] The primer layer on the coated substrate can be formed by applying the primer compositions disclosed herein using any of the methods disclosed herein. As such, the primer layer can include any of the additional ingredients in any of the amounts disclosed for the primer compositions described herein. In a specific example, the primer layer can include the polymer latex dispersion in an amount from 10 wt% to 70 wt% of all dry components of the primer layer.
Additionally, the polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax, and cationic salt can make up at least 80 wt% of all dry components of the primer layer.
[0043] In yet another example of the present technology, a printing system can include an inkjet ink and a coated media substrate as described above. The coated media substrate can include a media substrate and a primer layer coated on a surface of the media substrate. The primer layer can include a polyvinyl alcohol, starch nanoparticles, a polymer latex dispersion, a wax and a cationic salt. [0044] It is noted that, as used in this specification and the appended claims, the singular forms "a," "an," and "the" include plural referents unless the content clearly dictates otherwise.
[0045] "Substrate" or "media substrate" includes any base material that can be coated in accordance with examples of the present disclosure, such as film base substrates, polymer substrates, conventional paper substrates, photobase substrates, offset media substrates, and the like. Further, pre-coated and film coated substrates can be considered a "substrate" that can be further coated in accordance with examples of the present disclosure.
[0046] "Slip aid" refers to materials that can be added to coating compositions herein to provide abrasion resistance to coatings of the present disclosure.
[0047] "Instant dry smearfastness" refers to the ability of a printed image to resist smearing when rubbed with a dry instrument such as a finger or a Rubber Eraser Tool, immediately after printing or within a short time of being printed. The short time can be, for example, from 1 second to 30 seconds, from 1 second to 20 seconds, or from 5 seconds to 10 seconds. In some cases, the short time can be the time required for a printed image to travel from the inkjet printer to a rewinding roll. In one example, a printed image on an HP T230 Web Press® takes from 5 seconds to 10 seconds to reach the rewinder after being printed.
[0048] "Instant wet smearfastness" refers to the ability of a printed image to resist smearing when rubbed with a wet instrument such as a wet finger immediately after printing or within a short time of being printed. The short time can be, for example, from 1 second to 30 seconds, from 1 second to 20 seconds, or from 5 seconds to 10 seconds. In some cases, the short time can be the time required for a printed image to travel from the inkjet printer to a rewinding roll. In one example, a printed image on an HP T230 Web Press® takes from 5 seconds to 10 seconds to reach the rewinder after being printed.
[0049] "Instant mechability" refers to the instant dry and wet smearfastness and the scratch resistance of a sample after printing, drying, and reaching the rewinding station. [0050] When referring to "high speed" as it related to a digital printing press, presses such as the HP T230 Web Press® or the HP T350 Web Press® exhibit printing speeds that are commensurate of what is considered to be "high speed." For example, the HP T350 Web Press® can print text and/or other images on media at a rate of 400 feet per minute. This capability would be considered high speed. In another example, and more generally, printing at 100 feet per minute would also be considered high speed.
[0051 ]As used herein, the term "about" is used to provide flexibility to a numerical range endpoint by providing that a given value may be "a little above" or "a little below" the endpoint. The degree of flexibility of this term can be dictated by the particular variable and can be determined based on experience and the associated description herein.
[0052]As used herein, a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience. However, these lists should be construed as though each member of the list is individually identified as a separate and unique member. Thus, no individual member of such list should be construed as a de facto equivalent of any other member of the same list solely based on their presentation in a common group without indications to the contrary.
[0053] Concentrations, dimensions, amounts, and other numerical data may be presented herein in a range format. It is to be understood that such range format is used merely for convenience and brevity and should be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. For example, a weight ratio range of about 1 wt% to about 20 wt% should be interpreted to include not only the explicitly recited limits of 1 wt% and about 20 wt%, but also to include individual weights such as 2 wt%, 1 1 wt%, 14 wt%, and sub-ranges such as 10 wt% to 20 wt%, 5 wt% to 15 wt%, etc.
[0054] As a further note, in the present disclosure, it is noted that when discussing the coated media substrate, the method of coating a substrate, or the primer compositions herein, each of these discussions can be considered applicable to each of these examples, whether or not they are explicitly discussed in the context of that example. Thus, for example, in discussing details about the coated media substrate per se, such discussion also refers to the methods and primer compositions described herein, and wee versa.
[0055] The following examples illustrate some of the primer compositions, coated media substrates, systems, and methods that are presently known.
However, it is to be understood that the following are only exemplary or illustrative of the application of the principles of the present compositions, systems, and methods. Numerous modifications and alternative compositions, systems, and methods may be devised without departing from the spirit and scope of the present disclosure. The appended claims are intended to cover such modifications and arrangements. Thus, while the examples have been described above with particularity, the following provide further detail in connection with what are presently deemed to be the acceptable examples.
EXAMPLES [0056] Formulation Examples 1 -9 were prepared according to Tables 1 A and 1 B. Examples 7-9 are examples prepared according to the present technology and Examples 1 -6 are comparative examples.
Table 1 A
Example No. 1 2 3 4 5 Ingredient Dry Wt%
Poval® 4-88 2 2 2 2 (polyvinyl alcohol)
Poval® 18-88 9 18 9 9 9 (polyvinyl alcohol)
Penford® Gum 280 (starch) - - 4 - - Ecosphere® 2202D
(starch nanoparticles)
Polyvinyl pyrrolidone (30,000 Mw) - - - 4 -
Polyox™ N750 (polyethylene oxide) - - - - 4
Litex® 9710 50 45 48 48 48
(carboxylated styrene-butadiene
copolymer latex)
Ultralube® D-806 1 1 10 10 10 10 (polyethylene wax)
Calcium Chloride 27 26 26 26 26 (cationic salt)
TEGO® Wet 510 1 1 1 1 1 (surfactant)
Table 1 B
Example No. 6 7 8 9 Ingredient Dry Wt%
Poval® 4-88 2
(polyvinyl alcohol)
Poval® 18-88 4 9 9 (polyvinyl alcohol)
Penford® Gum 280 (starch) - - - -
Ecosphere® 2202D 1 1 9 4 4 (starch nanoparticles)
Polyvinyl pyrrolidone (30,000 Mw) - - - -
Polyox™ N750 (polyethylene oxide) - - - -
Litex® 9710 50 50 48 50
(carboxylated styrene-butadiene
copolymer latex)
Ultralube® D-806 1 1 10 10 10 (polyethylene wax) Calcium Chloride 27 26 26 26
(cationic salt)
TEGO® Wet 510 1 1 1 1
(surfactant)
Poval® (from Kuraray America, Inc.)
Ultralube® (from Keim-Additec Surface GmbH)
TEGO® (from Evonik Resource Efficiency GmbH)
Ecosphere® (from EcoSynthetix Inc.)
Litex® (from Synthomer LLC)
Polyox™ (from Dow Chemical Company)
Penford® Gum (from Penford Products Co.)
[0057] The Example formulations 1 -9 were coated onto Sterling® Ultra Gloss (Verso Corporation), 60# paper with 2 g/m2 (gsm) of dry coating weight. Samples were printed with an HP CM8060 M FP Edgeline printer, from Hewlett- Packard Co., Palo Alto, CA, USA (HP), using HP A50 pigment inks (i.e. aqueous inkjet ink for digital inkjet printing). The printing process used involved 2 passes and six dry spin conditions to mimic high-speed, digital, web press inkjet printing. Dry and wet smearfastness refer to the ability of the printed image to resist appearance degradation upon rubbing or smearing the image by dry or wet finger. For the dry and wet finger smearfastness tests, a dry or wet finger was placed against a printed area, pushed with force of about 50 g/in2, and drawn toward the tester. The finger was then released to check the tested area.
[0058]The results of the dry finger smearfastness test and wet finger smearfastness test are shown in Table 2. For the dry and wet finger
smearfastness tests, the visual ranking is based on a 1 to 5 scale, with 1 being the worst and 5 being the best. A ranking equal to or greater than 3 is considered good and acceptable. A ranking below 3 is considered poor and not acceptable.
Table 2: Visual Ranking of Performance
Example No. Dry Finger Smearfastness Wet Finger Smearfastness 1 3.5 2.5
2 3.5 2.5
3 3 2.5
4 3.25 2.5
5 3.25 2.5
6 1 .5 1 .5
7 2.5 4
8 3.5 3
9 3.25 3
[0059] Examples 1 -5 did not include starch nanoparticles. These examples did not provide sufficient wet finger smearfastness. Example 6 included starch nanoparticles, but no polyvinyl alcohol. This example showed very poor dry finger smearfastness and wet finger smearfastness. Examples 7-9 included both starch nanoparticles and polyvinyl alcohol (as well as latex particles). Example 7 provided excellent wet finger smearfastness but marginal dry finger
smearfastness. Examples 8 and 9 both provided good dry finger smearfastness and wet finger smearfastness. Therefore, these examples show that, although neither starch nanoparticles nor polyvinyl alcohol can provide sufficient wet and dry smearfastness when used alone, the combination of these two binders, along with latex particles) unexpectedly provides good wet and dry smearfastness.
[0060]While the disclosure has been described with reference to certain examples, various modifications, changes, omissions, and substitutions can be made without departing from the spirit of the disclosure. It is intended, therefore, that the disclosure be limited only by the scope of the following claims.

Claims

CLAIMS What Is Claimed Is:
1 . A primer composition, comprising:
5 wt% to 70 wt% of a binder including polyvinyl alcohol, starch
nanoparticles, and a polymer latex dispersion;
a wax;
a cationic salt; and
water.
2. The primer composition of claim 1 , wherein the polymer latex dispersion is selected from an SBR-based latex dispersion, a cationic acrylate latex disperison, a polyvinyl acetate latex dispersion, and combinations thereof.
3. The primer composition of claim 2, wherein the starch nanoparticles are crosslinked starch nanoparticles.
4. The primer composition of claim 1 , wherein the cationic salt is present in an amount from 10 wt% to 50 wt% of all dry components of the primer composition.
5. The primer composition of claim 1 , wherein the cationic salt comprises a cation of a metal selected form the group consisting of sodium, calcium, copper, nickel, magnesium, zinc, barium, iron, aluminum and chromium.
6. The primer composition of claim 1 , wherein the polymer latex dispersion is present in an amount from 10 wt% to 70 wt% of all dry components of the primer composition.
7. The primer composition of claim 6, wherein the polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax, and cationic salt make up at least 80 wt% of all dry components of the primer composition.
8. The primer composition of claim 1 , wherein the polyvinyl alcohol is a mixture of two different polyvinyl alcohols with different weight-average molecular weights.
9. The primer composition of claim 1 , wherein the primer composition further comprises an inorganic pigment in an amount of about 5 wt% or less of all dry components of the primer composition.
10. A method of coating a media substrate, comprising applying a primer composition to a media substrate, wherein the primer composition comprises:
from 5 wt% to 70 wt% binder including polyvinyl alcohol, starch
nanoparticles, and a polymer latex dispersion;
a wax;
cationic salt; and
water.
1 1 . The method of claim 10, wherein the polymer latex dispersion is present in an amount from 10 wt% to 70 wt% of all dry components of the primer composition, and wherein the polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax, and cationic salt make up at least 80 wt% of all dry components of the primer composition.
12. The method of claim 10, wherein the starch nanoparticles are crosslinked starch nanoparticles.
13. A coated media substrate, comprising:
a media substrate; and an ink-receiving primer layer coated on a surface of the media substrate, the primer layer comprising:
from 5 wt% to 90 wt% binder including polyvinyl alcohol, starch nanoparticles, and a polymer latex dispersion;
a wax; and
a cationic salt.
14. The coated media substrate of claim 13, wherein the media substrate is a smooth, nonporous offset media substrate.
15. The coated media substrate of claim 13, wherein the starch nanoparticles are crosslinked starch nanoparticles, wherein the polymer latex dispersion is present in an amount from 10 wt% to 70 wt% of all dry components of the primer layer, and wherein the polyvinyl alcohol, starch nanoparticles, polymer latex dispersion, wax, and cationic salt make up at least 80 wt% of all dry components of the primer layer.
PCT/US2015/047447 2015-08-28 2015-08-28 Primer compositions WO2017039585A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP15903176.4A EP3265318B1 (en) 2015-08-28 2015-08-28 Primer compositions
US15/569,511 US20180087222A1 (en) 2015-08-28 2015-08-28 Primer compositions
CN201580080539.5A CN107690499B (en) 2015-08-28 2015-08-28 Primer composition
PCT/US2015/047447 WO2017039585A1 (en) 2015-08-28 2015-08-28 Primer compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2015/047447 WO2017039585A1 (en) 2015-08-28 2015-08-28 Primer compositions

Publications (1)

Publication Number Publication Date
WO2017039585A1 true WO2017039585A1 (en) 2017-03-09

Family

ID=58188215

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2015/047447 WO2017039585A1 (en) 2015-08-28 2015-08-28 Primer compositions

Country Status (4)

Country Link
US (1) US20180087222A1 (en)
EP (1) EP3265318B1 (en)
CN (1) CN107690499B (en)
WO (1) WO2017039585A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102021106141A1 (en) 2021-03-12 2022-09-15 Adesiv GmbH Water-based dispersion paint system and use of the dispersion paint system and substrate

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102156031B1 (en) * 2015-08-28 2020-09-15 휴렛-팩커드 디벨롭먼트 컴퍼니, 엘.피. Primer composition
CN110424182A (en) * 2019-07-08 2019-11-08 浙江金龙纸业有限公司 Environmentally friendly compounding Cypres of one kind and preparation method thereof
WO2021050071A1 (en) * 2019-09-12 2021-03-18 Hewlett-Packard Development Company, L.P. Pre-treatments for packaging print media
EP3967802B1 (en) * 2020-09-11 2023-03-29 Basf Se Consolidated nonwoven

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5084492A (en) * 1989-09-28 1992-01-28 Standard Register Company High solids cf printing ink
US5102856A (en) * 1990-11-07 1992-04-07 The Standard Register Company High solids self-contained printing ink
US20030021962A1 (en) * 2001-04-20 2003-01-30 Debabrata Mukherjee Ink jet printable heat transfer paper
US20060014014A1 (en) * 2002-09-04 2006-01-19 Van Den Abbeele Henk Jan F Vapor screen composition
US20140212591A1 (en) * 2013-01-31 2014-07-31 Hewlett-Packard Development Company, L.P. Pre-treatment coating

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1176255A1 (en) * 2000-07-24 2002-01-30 The Dow Chemical Company Use of starch dispersions as binder in coating compositions and process for preparing the starch dispersions
CN1981316A (en) * 2004-06-08 2007-06-13 艾利丹尼森公司 Method of providing printable decorative labels for customization of portable electronic devices
US9132686B2 (en) * 2008-05-27 2015-09-15 Hewlett-Packard Development Company, L.P. Media for use in inkjet printing
BR112012002250B1 (en) * 2009-07-31 2020-11-03 Hewlett - Packard Development Company, Lp coating composition, method for making a coating composition, media sheet and method for forming a media sheet
US8449665B2 (en) * 2010-01-08 2013-05-28 Hewlett-Packard Development Company, L.P. Coating compositions including starch nanoparticles
US8821998B2 (en) * 2012-04-13 2014-09-02 Newpage Corporation Recording medium for inkjet printing
US9286530B2 (en) * 2012-07-17 2016-03-15 Cognex Corporation Handheld apparatus for quantifying component features
EP2951026B1 (en) * 2013-01-31 2018-03-21 Hewlett-Packard Development Company L.P. Pre-treatment coating
CN104968741B (en) * 2013-01-31 2017-04-12 惠普发展公司,有限责任合伙企业 Swellable pre-treatment coating
EP3099511B1 (en) * 2014-01-30 2020-10-28 Hewlett-Packard Development Company, L.P. Print media for inkjet printing

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5084492A (en) * 1989-09-28 1992-01-28 Standard Register Company High solids cf printing ink
US5102856A (en) * 1990-11-07 1992-04-07 The Standard Register Company High solids self-contained printing ink
US20030021962A1 (en) * 2001-04-20 2003-01-30 Debabrata Mukherjee Ink jet printable heat transfer paper
US20060014014A1 (en) * 2002-09-04 2006-01-19 Van Den Abbeele Henk Jan F Vapor screen composition
US20140212591A1 (en) * 2013-01-31 2014-07-31 Hewlett-Packard Development Company, L.P. Pre-treatment coating

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102021106141A1 (en) 2021-03-12 2022-09-15 Adesiv GmbH Water-based dispersion paint system and use of the dispersion paint system and substrate

Also Published As

Publication number Publication date
EP3265318A4 (en) 2018-01-10
EP3265318A1 (en) 2018-01-10
CN107690499B (en) 2021-04-27
CN107690499A (en) 2018-02-13
US20180087222A1 (en) 2018-03-29
EP3265318B1 (en) 2019-10-02

Similar Documents

Publication Publication Date Title
US11365325B2 (en) Primer compositions
EP3265318B1 (en) Primer compositions
EP2951026B1 (en) Pre-treatment coating
EP2762533B1 (en) Pre-Treatment Coating
EP2701922A1 (en) Recording media
JP2005022415A (en) Inkjet recording material containing siloxane copolymer surfactant
US10414937B2 (en) Pre-treatment coating compositions
EP3265319B1 (en) Primer compositions
US20180086935A1 (en) Primer compositions
US10759963B2 (en) Pre-treatment coating compositions
WO2016118161A1 (en) Coated print media
WO2021050103A1 (en) Pre-treatments for publishing print media
EP3341207A1 (en) Coated print media
CN107921806B (en) Sizing composition
WO2016105413A1 (en) Coated print medium
JP2004050554A (en) Inkjet recording sheet

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 15903176

Country of ref document: EP

Kind code of ref document: A1

REEP Request for entry into the european phase

Ref document number: 2015903176

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 15569511

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE