Ink composition for use on non-absorbent surfaces

Abstract

According to one aspect, an ink composition includes a colorant, one or more polymers such as a polyurethane siloxane, a surfactant, water, and a solvent. The ink composition has a total solids content of less than about 20% by weight. Further the ink has an initial surface tension of less than about 50 dynes per centimeter on application and the surface tension on drying should not increase by more than 20 percent.

Claims

1. An aqueous ink comprising: a first urethane silanol polymer and a second urethane silanol polymer; from about 0.5 to about 12% by weight of one or more colorants; from about 5 to about 35% by weight of a solvent; from about 0.03 to about 1.0% by weight of a pH modifier; and water, wherein the aqueous ink has a viscosity such that the aqueous ink can be applied to a non-absorbent surface layer, wherein the first urethane silanol polymer is polycarbonate based and is about 5.5% by weight and the second urethane silanol polymer is polyester based and is about 0.3% by weight.

2. The aqueous ink of claim 1, wherein the viscosity is from about 1 to about 20 mPa-s.

3. The aqueous ink of claim 1, further comprising from about 0.1 to about 5% by weight of a surfactant.

4. The aqueous ink of claim 1, further comprising from about 1 to about 20% by weight of a crosslinker.

5. The aqueous ink of claim 4, wherein the crosslinker is an iso-cyanate crosslinker.

6. The aqueous ink of claim 1, wherein the first urethane silanol and the second urethane silanol polymer are a self-crosslinking urethane silanol polymers.

7. The aqueous ink of claim 1, wherein the solvent is chosen from the group consisting of 1-(2-hydroxyethyl)-2-pyrrolidone, alcohols, polyols, glycerols, and glycols.

8. The aqueous ink of claim 4, wherein the surfactant is an ethoxylated molecule.

9. The aqueous ink of claim 1, wherein the pH modifier is dimethylethanolamine.

10. The aqueous ink of claim 1, wherein the ink has a dynamic surface tension at 25 degrees Celsius from about 20 to about 45 dynes/cm.

11. A method for high speed variable printing comprising the steps of: providing an aqueous ink, the aqueous ink comprising: a first urethane silanol polymer and a second urethane silanol polymer, wherein the first urethane silanol polymer is polycarbonate based and is about 5.5% by weight and the second urethane silanol polymer is polyester based and is about 0.3% by weight; from about 0.5 to about 12% by weight of a pigment; from about 5 to 35% by weight of a solvent; from about 0.03 to about 1.0% by weight of a pH modifier; and water, wherein the aqueous ink has a viscosity from about 1 to about 20 mPa-s; and applying the aqueous ink onto a non-absorbent substrate in a first layer.

12. The method of claim 11, the method further comprising the step of applying the aqueous ink in a plurality of further layers.

13. The method of claim 11, wherein the aqueous ink further comprises from about 0.1 to about 5.0% by weight of a surfactant.

14. The method of claim 11, the method further comprising the step of applying heat to crosslink the first urethane silanol polymer and the second urethane silanol polymer of the aqueous ink.

15. The aqueous ink of claim 1, wherein the aqueous ink has a ratio of colorant to polymer between about 2:1 and about 1:2 by weight.

16. The aqueous ink of claim 1, wherein the aqueous ink has a total solids content of less than about 20% by weight.

17. The aqueous ink of claim 2, wherein the aqueous ink has a viscosity from about 4 to 14 mPa-s.

Description

DETAILED DESCRIPTION

(1) An ink composition of the present application includes a colorant, a polyurethane siloxane, a solvent, water, and optionally a crosslinker. The ink composition has a total solids content of less than about 20% by weight, and a ratio of colorant to polyurethane between about 2:1 and 1:2 by weight. Further the ink has an initial surface tension of less than about 50 dynes per centimeter on application and the surface tension on drying should not increase by more than 20%.

(2) Such ink composition is suitable for use in a variety of high-speed printing systems. A non-absorbent print medium, such as metal foils, ceramics, plastics, highly coated papers or other similar substrates, receives ink using a variety of printing methods.

(3) The ink composition has a viscosity such that the ink composition can be applied to a substrate using a variety of printing methods. The viscosity may range from about 1.0 to 20.0 cP, preferably from about 4.0 cP to about 6.0 cP, although the preferred viscosity may depend in part on the requirements of the print system to be used.

(4) One important aspect of the present composition is that the initial surface tension of the ink be less than 50 dynes/cm. At this surface tension the ink will properly spread on the non-absorbent surface. It is preferred that the surface tension be less than 40 dynes/cm. Another important aspect is that on drying the surface tension of the ink not increase dramatically. It has been found that if the surface tension changes too greatly upon drying, the physical properties of the ink on the non-absorbent surface are degraded. In particular, the solvent resistance, the rub resistance and leveling of the ink on the non-absorbent surface are not satisfactory if the surface tension changes too much, more than 20%, on drying.

(5) Suitable surface active agents to provide the above surface tension properties include nonionic compounds comprised of silicone, ethylene oxide (EO), and propylene oxide (PO) such as Silwet Hydrostable 212, available from Momentive Performance Products (Albany, N.Y.), fluorinated nonionics such as Multiwet VE-LQ-(AP), available from Croda Industrial Chemicals (East Yorkshire, England) and the like. These surface active agents can be present in amounts ranging from about 0.1 to 3.0% by weight, more preferably less than 1.0% by weight.

(6) In other embodiments, the surfactant or surface modifying agent may include, for example, nonionic surfactants, such as poloxamer, ethoxylated acetylenediol, ethoxylated alcohols, or other ethoxylated surfactants. Any type of surfactant may be useful to include in the ink composition to impart the desired properties including anionic, nonionic, cationic, or other types of surfactants. In addition, leveling agents also can act as surface modifying agents in an amount of up to about 2.5% by weight.

(7) The ethoxylated acetylenediol based surfactants suitable for use include Air Products' Surfynol 400 series surfactants: Surfynol 420, 440, 465, and 485, respectively. The Surfynol 400 series surfactants by Air Products (Allentown, Pa.) are produced by reacting various amounts of ethylene oxide with 2,4,7,9-tetra-methyl-5-decyne-4,7-diol (Air Products' Surfynol 104), a nonionic molecule with a hydrophilic section in the middle of two symmetric hydrophobic groups.

(8) The ethoxylated alcohols based surfactants suitable for use include Tomadol series surfactants by Air Products (Allentown, Pa.). Tomadol ethoxylated alcohols are produced by a base-catalyzed condensation reaction of ethylene oxide with an alcohols of varying chain lengths ranging from C.sub.9 to C.sub.15.

(9) In one embodiment, the ink composition may be printed in a heated environment of about 120 degrees Fahrenheit (50 degrees Celsius).

(10) In another embodiment the ink composition may be printed onto a substrate and heated by a platen. The platen may be heated to a temperature of about 100 degrees Fahrenheit (40 degrees Celsius) or to a temperature of about 120 degrees Fahrenheit (50 degrees Celsius). The substrate is then heated to a temperature greater than 220 degrees Fahrenheit (100 degrees Celsius) for about ten minutes to unblock and enable crosslinking. The ink is then cured at about 300 degrees Fahrenheit (150 degrees Celsius) for ten minutes.

(11) Appropriate thickness is achieved by printing multiple layers prior to curing. The ink composition may be disposed in a layer having a thickness in the range from about 5 microns to about 15 microns. The desired ink thickness may be obtained by printing a number of layers of ink onto the substrate. In some embodiments, the thickness may be obtained by printing up to about 50 layers, preferably up to about 30 layers, and more preferably up to about 15 layers of ink over the substrate, although the number of layers depends on various factors such as, for example, selection of the means for applying the ink, fluid solids content of the ink composition, and mass flow rate.

(12) The polymer (polyurethane siloxane) acts as a binder to stabilize the colorant on the print medium and provides increased long term durability of a final product. Immediate durability refers to the ability of the ink composition to bond to the print medium quickly and move through a high speed printing press without transferring to elements of the press.

(13) Suitable polymers for the ink composition of the present application include urethane resin emulsions having a silanol group or a group capable of preparing a silanol group by hydrolysis, such urethane resins include Takelac WS-5000 (polyester based), Takelac WS-5100 (polycarbonate based), Takelac WS-4000 (polycarbonate based), and Takelac WS-6021 (polyether based), manufactured by Mitsui Chemicals, Inc. (Tokyo, Japan). These are self-crosslinking polyurethane dispersions that form siloxane bonds with the evaporation of water. Polymers may be self-crosslinking through heat and/or hydrolysis. Polymers may also be crosslinked via one or more crosslinkers or catalysts.

(14) In certain embodiments, suitable crosslinkers include blocked isocyanates wherein the application of heat enables crosslinking. A suitable crosslinker is Trixene Aqua BI 201 by Baxenden Chemicals Limited (Lancashire, England). This crosslinker becomes unblocked between 110 and 120 degrees Celsius.

(15) Certain embodiments comprise an epoxy binder. Suitable epoxy resins include DER 684-EK40 by Dow Chemical Company (Midland, Mich.). This resin is formed by reacting epichlorohydrin with bisphenol A to form diglycidyl ethers of bisphenol A.

(16) The colorant may be any conventional pigment or dye commercially available. Examples of suitable colorants include but, are not limited to, carbon black colorant such as Pro-Jet Black APD1000 by FujiFilm (New Castle, Del.), magenta colorant such as Cab-O-Jet 465 by Cabot Corp. (Boston, Mass.), cyan colorant such as Cab-O-Jet 450 or 452 by Cabot Corp. (Boston, Mass.), or yellow colorant such as Cab-O-Jet 470 by Cabot Corp. (Boston, Mass.) visibly opaque infra-red transmitting dyes such as Epolight 7527A by Epolin, Inc. (Newark, N.J.), white colorants composed of titanium dioxide such as Cyclojet White Ti-7510 and Cyclojet White TI-7530 by Lever Colors (Bensalem, Pa.), opacifiers such as Ludox AS 40 by Grace (Columbia, Md.), and metallic colorants containing aluminum, silver, or gold such as Jetfluid SB11025 and Jetfluid SB11028 by Eckart GmbH (Hartenstein, Germany).

(17) Visibly opaque infra-red transmitting dyes, such as Epolight 7527A, should transmit greater than 80% of light having a wavelength greater than 850 nm and should transmit between 5 and 15% of light having a wavelengths less than 550 nm.

(18) The total solids content of the ink composition is less than about 20% by weight. The ink composition may include about 0.5 to about 12 percent by weight of a colorant and about 3 to about 15 percent by weight of a polymer (polyurethane siloxane) and crosslinker. The ratio of colorant to polymer and crosslinker may range from about 2:1 to about 1:2.

(19) The ink composition of the present application may include water as a solvent. The composition may also include a water-soluble organic compound as a co-solvent. Suitable water-soluble or miscible organic components include: glycerin; alcohols, such as methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, sec-butyl alcohol, or tert-butyl alcohol; amides, such as dimethylformamide or dimethylacetamide; carboxylic acids; esters, such as ethyl acetate, methyl lactate, ethyl lactate, propyl lactate and ethylene carbonate; ethers, such as 2-butoxyethanol, tetrahydrofuran or dioxane; glycols, such as propylene glycol, and diethylene glycol; glycol esters; glycol ethers, such as propylene glycol methyl ether, dipropylene glycol methyl ether; ketones, such as acetone, diacetone, or methyl ethyl ketone; lactams, such as N-isopropyl caprolactam or N-ethyl valerolactam, 2-pyrrolidinone, N-methylpyrrolidinone, or N-(2-hydroxyethyl)-2-pyrrolidone; lactones, such as butyrolactone; organosulfides; sulfones, such as dimethylsulfone; organosulfoxides, such as dimethyl sulfoxide or tetramethylene sulfoxide; and derivatives thereof and mixtures thereof.

(20) Additional contemplated components in the ink composition include a solvent, a preservative such as Proxel GXL by Arch Biocides (Smyrna, Ga.), a humectant (e.g. propylene glycol), a biocide, a colorant, a polymer, a leveling agent, a salt, an inorganic compound, an organic compound, water, a viscosity adjuster such as Walocel CRT 30 by Dow Chemical Company (Midland, Mich.), a pH modifier such as diethanolamine or triethanolamine, and/or any combination thereof.

(21) The following examples further illustrate the disclosure but, of course, should not be construed as in any way limiting its scope.

EXAMPLE 1

(22) A black ink composition useful in the present disclosure was prepared having the following formulation:

(23) 35.7% by weight carbon black dispersion (Fuji APD 1000 Carbon Black) (14% solids),

(24) 28.4% by weight deionized water,

(25) 19.0% by weight polymer dispersion (Takelac AC WS-4000) (29% solids),

(26) 15.0% by weight humectant (2-hydroxyethyl pyrrolidone),

(27) 1.0% by weight polymer dispersion (Takelac AC WS-5000) (30% solids),

(28) 0.8% by weight surfactant (Silwet Hydrostable 212), and

(29) 0.08% by weight pH modifier (dimethylethanolamine)

(30) The water and hydroxyethyl pyrrolidone (HEP) were vigorously mixed and the polymer, pH modifier, and pigment were added very slowly. Later, the surfactant was added. After an additional period of vigorous mixing, the ink was finely filtered with a common filter system known to those having ordinary skill in the art of ink production.

(31) Viscosity of the ink at 32 degrees Celsius was 5.13 cP and the pH was 9.08. Surface tension at 25 degrees Celsius was 36.0 dynes/cm as measured using a SensaDyne tensiometer.

EXAMPLE 2

(32) A black infrared transmitting ink composition useful in the present disclosure was prepared having the following formulation:

(33) 42.9% by weight deionized water,

(34) 25.0% by weight polymer dispersion (Takelac AC WS-4000) (29% solids),

(35) 17.0% by weight humectant (2-hydroxyethyl pyrrolidone),

(36) 10.0% by weight colloidal silica dispersion (Ludox AS-40) (40% solids),

(37) 5.0% by weight visibly opaque IR transmitting dye solution (20% Epolight 7527A in hydroxyethyl pyrrolidone solution), and

(38) 0.1% by weight pH modifier (dimethylethanolamine)

(39) The dye solution and HEP were vigorously mixed and the polymer was added very slowly. After a period of vigorous mixing, the deionized water was added. Subsequently, the pH modifier was added and later the crosslinker was added. After a period of mixing, the silica dispersion was added and after an additional period of vigorous mixing, the ink was filtered.

(40) Viscosity of the ink at 32 degrees Celsius was 4.50 cP and the pH was 9.72. Surface tension at 25 degrees Celsius was 56.0 dynes/cm.

EXAMPLE 3

(41) A first white ink composition useful in the present disclosure was prepared having the following formulation:

(42) 33.7% by weight deionized water,

(43) 19.7% by weight humectant (2-hydroxyethyl pyrrolidone),

(44) 14.8% by weight titanium oxide dispersion (Cyclojet White TI-7510),

(45) 12.7% by weight polymer dispersion (Takelac AC WS-4000) (29% solids),

(46) 11.9% by weight crosslinker dispersion (Trixene BI 201) (40% solids),

(47) 6.4% by weight colloidal silica dispersion (Ludox AS-40) (40% solids),

(48) 0.4% by weight pH modifier (dimethylethanolamine, 50% in water),

(49) 0.3% by weight surfactant (Silwet Hydrostable 212), and

(50) 0.3% by weight preservative (Proxel GXL)

(51) The titanium oxide dispersion and the silica dispersion were mildly mixed and the polymer and crosslinker were added very slowly. After mild mixing, the deionized water, HEP, and preservative were added, after another period of mild mixing, the pH modifier was added. Then, the surfactant was added, and after mixing, the ink was filtered.

(52) The ink composition was 16.4% solids. Viscosity of the liquid ink at 32 degrees Celsius was 4.92 cP and the pH was 9.2. Surface tension at 25 degrees Celsius was 43.68 dynes/cm.

EXAMPLE 4

(53) A second white ink composition useful in the present disclosure was prepared having the following formulation:

(54) 44.5% by weight deionized water,

(55) 23.4% by weight polymer dispersion (Takelac AC WS-4000) (29% solids),

(56) 15.4% by weight titanium oxide dispersion (Cyclojet White TI-7530),

(57) 7.7% by weight humectant (2-hydroxyethyl pyrrolidone),

(58) 3.0% by weight surface tension modifier (2-butoxy ethanone),

(59) 3.4% by weight humectant (ethylene glycol),

(60) 1.7% by weight levelling agent (Silwet Hydrostable 212),

(61) 0.7% by weight surfactant (Surfynol 465),

(62) 0.1% by weight pH modifier (dimethylethanolamine), and

(63) 0.08% by weight preservative (Proxel GXL)

(64) The ink composition was 14.7% solids. Viscosity of the liquid ink at 32 degrees Celsius was 6.03 cP and the pH was 8.6. Surface tension at 25 degrees Celsius was 31.44 dynes/cm.

EXAMPLE 5

(65) A metallic ink composition useful in the present disclosure was prepared having the following formulation:

(66) 85.4% by weight aluminum dispersion (Eckart Jetfluid SB11028),

(67) 9.5% by weight solvent (dimethyl sulfoxide), and

(68) 5.1% by weight polymer solution (DER 684-EK40 epoxy resin, 20% solids in dimethyl sulfoxide)

(69) The aluminum dispersion, the polymer, and the aprotic solvent were mildly mixed. After a period of mild mixing, the ink was filtered.

(70) The ink composition was 4% solids. Viscosity of the ink at 32 degrees Celsius was 4.98 cP. Dynamic surface tension at 25 degrees Celsius was 31.8 dynes/cm, and static surface tension was 29.7 dynes/cm.

(71) All of the fonnulations of Examples 1-5 produced valuable printing inks with acceptable immediate and long term durability.

INDUSTRIAL APPLICABILITY

(72) 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.

(73) The use of the terms a and an and the and similar references 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 disclosure and does not pose a limitation on the scope of the disclosure unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the disclosure. Numerous modifications to the present disclosure will be apparent to those skilled in the art in view of the foregoing description. It should be understood that the illustrated embodiments are exemplary only, and should not be taken as limiting the scope of the disclosure.