Patent Application
20160177111
Disclosed herein is a nanosilver ink composition. More particularly, disclosed herein is a nanosilver ink composition comprising silver nanoparticles; a clay dispersion; and an ink vehicle.
Xerox Corporation has invented a nanosilver particle which is stabilized by an organoamine. U.S. Pat. No. 8,765,025, which is hereby incorporated by reference herein in its entirety, describes a metal nanoparticle composition includes an organic-stabilized metal nanoparticle and a solvent in which the solvent selected has the following Hansen solubility parameters: a dispersion parameter of about 16 MPa0.5, or more, and a sum of a polarity parameter and a hydrogen bonding parameter of about 8.0 MPa0.5 or less. U.S. Pat. No. 7,270,694, which is hereby incorporated by reference herein in its entirety, describes a process for preparing stabilized silver nanoparticles comprising reacting a silver compound with a reducing agent comprising a hydrazine compound by incrementally adding the silver compound to a first mixture comprising the reducing agent, a stabilizer comprising an organoamine, and a solvent.
U.S. patent application Ser. No. 13/866,704, which is hereby incorporated by reference herein in its entirety, describes stabilized metal-containing nanoparticles prepared by a first method comprising reacting a silver compound with a reducing agent comprising a hydrazine compound by incrementally adding the silver compound to a first mixture comprising the reducing agent, a stabilizer comprising an organoamine, and a solvent. U.S. patent application Ser. No. 14/188,284, which is hereby incorporated by reference herein in its entirety, describes conductive inks having a high silver content for gravure and flexographic printing and methods for producing such conductive inks.
Inks have been successfully formulated in non-polar solvents such as decalin and bicyclohexane and successfully printed using inkjet printing technologies. As printed electronics matures and moves to higher volume production, it is desirable to have inks that can be used in offset printing technologies such as flexography and gravure. Offset printing technologies provide ready established printing processes and equipment.
A gravure printing process is very similar to flexography except that it does not have an anilox roller and the image is engraved onto a metal cylinder. This makes gravure more expensive than flexo and high volume printing. One of the main advantages of gravure over flexo is the ability to consistently make high quality prints.
A need remains for inks that can be successfully employed in these offset technologies for printed electronics applications. Current inks include high loadings of silver nanoparticles, such as from about 50 to about 70 percent. Such inks have a very low viscosity, such as from about 8 to about 12 centipoise and typically greater than about 10 centipoise.
Gravure and flexographic processes provide a potentially efficient way to manufacture a number of conductive components at a lower cost than that of other printing applications. However, when used for flexographic printing, the low viscosity of current ink compositions results in very thin films, such as less than about 500 nanometers, and a minimum line width of about 125 nanometers. Thin, highly conductive films are good for certain applications such as memory devices.
However, there are a number of applications that require thicker films, such as RFID (Radio Frequency Identification) antennas which require a film having a thickness of about 10 to about 20 micrometers. When low viscosity ink is used in gravure printing processes, the ink overspreads. Higher viscosity ink is desired to print thicker films and to improve line resolution for flexographic printing and to prevent smearing for gravure printing. The current method for increasing ink viscosity is to increase silver loading, such as to from about 65 to about 75 percent. However, this is a costly solution which does not provide an adequate increase to ink viscosity. A need remains for an improved ink composition that can provide an adequate ink viscosity without negatively impacting ink performance.
The appropriate components and process aspects of each of the foregoing U. S. patents and Patent Publications may be selected for the present disclosure in embodiments thereof. Further, throughout this application, various publications, patents, and published patent applications are referred to by an identifying citation. The disclosures of the publications, patents, and published patent applications referenced in this application are hereby incorporated by reference into the present disclosure to more fully describe the state of the art to which this invention pertains.
Described is a nanosilver ink composition comprising silver nanoparticles; a clay dispersion; and an ink vehicle.
Also described is a process for preparing a nanosilver ink composition comprising combining silver nanoparticles; a clay dispersion; and an ink vehicle.
Also described is a process for forming conductive features on a substrate comprising providing a nanosilver ink composition comprising silver nanoparticles; a clay dispersion; and an ink vehicle; depositing the nanosilver ink composition onto a substrate to form deposited features; and heating the deposited features on the substrate to form conductive features on the substrate.
A nanosilver ink composition comprising silver nanoparticles; a clay dispersion; and an ink vehicle is provided.
Silver Nanoparticles. The ink composition herein comprises silver nanoparticles. The silver nanoparticles may have any shape or geometry. In embodiments, the silver nanoparticles have a spherical shape. The silver nanoparticles can have a diameter in the submicron range. In embodiments, the silver nanoparticles have a volume average particle size of from about 0.5 to about 100 nanometers (nm), or from about 1.0 to about 50 nm, or from about 1.0 to about 20 nm. The characteristics of the silver nanoparticles may be determined by any suitable technique and apparatus. Volume average particle diameter may be measured by means of a measuring instrument such as a light scattering particle sizer, operated in accordance with the manufacturer's instructions. Volume average particle diameter may also be measured by means of a measuring instrument such as a Beckman Coulter Multisizer 3, operated in accordance with the manufacturer's instructions.
The silver nanoparticles may be elemental silver, a silver alloy, or a combination thereof. In embodiments, the silver nanoparticles may be a base material coated or plated with pure silver, a silver alloy, or a silver compound. For example, the base material may be copper flakes with silver plating. The silver alloy may be formed from at least one metal selected from Au, Cu, Ni, Co, Pd, Pt, Ti, V, Mn, Fe, Cr, Zr, Nb, Mo, W, Ru, Cd, Ta, Re, Os, Ir, Al, Ga, Ge, In, Sn, Sb, Pb, Bi, Si, As, Hg, Sm, Eu, Th, Mg, Ca, Sr, and Ba, although not limited.
In embodiments, the silver compound may include either or both of (i) one or more other metals and (ii) one or more non-metals. Suitable other metals include, for example, Al, Au, Pt, Pd, Cu, Co, Cr, In, and Ni, particularly the transition metals, for example, Au, Pt, Pd, Cu, Cr, Ni, and mixtures thereof. Exemplary metal composites are Au—Ag, Ag—Cu, Au—Ag—Cu, and Au—Ag—Pd. Suitable non-metals in the metal composite include, for example, Si, C, and Ge. In certain embodiments the silver nanoparticles are composed of elemental silver. In embodiments, the silver particles can be selected from those described in U.S. patent application Ser. No. 14/188,284, which is hereby incorporated by reference herein in its entirety.
The silver nanoparticles can be stabilized metal-containing nanoparticles as described in U.S. patent application Ser. No. 13/866,704, which is hereby incorporated by reference herein in its entirety. In embodiments, the stabilized metal-containing nanoparticles are prepared by a first method comprising reacting a silver compound with a reducing agent comprising a hydrazine compound by incrementally adding the silver compound to a first mixture comprising the reducing agent, a stabilizer comprising an organoamine, and a solvent. In embodiments, the stabilized metal-containing nanoparticles are prepared by a second method comprising reacting a silver compound with a reducing agent comprising providing a second reaction mixture of the silver compound and the stabilizer, and adding the reducing agent to the second reaction mixture, wherein the silver compound, the stabilizer, and the reducing agent are the same in the first method and the second method. Stabilized metal-containing nanoparticles that contain silver and/or a silver alloy composite are prepared by reacting a silver compound and/or a silver complex with a reducing agent at a temperature between about 20° C. and about 60° C. The reaction is carried out by incrementally adding the silver compound or a mixture of the silver compound and a stabilizer to a solution containing (a) the reducing agent, which includes a hydrazine compound, (b) a stabilizer, which includes an organoamine, and (c) a solvent. Stabilized silver nanoparticles can be prepared by a process including (a) providing a mixture of a reducing agent, a stabilizer, and a solvent; and (b) (i) incrementally adding a silver compound to the mixture or (ii) incrementally adding a complex comprising a silver compound and an organoamine stabilizer to the mixture, wherein the temperature of the mixture is maintained below about 60° C., and wherein a soluble silver ion concentration remains low in the mixture. For further detail, see U.S. patent application Ser. No. 13/866,704.
The silver nanoparticles can be stabilized metal-containing nanoparticles prepared as described in U.S. Pat. No. 7,270,694, which is hereby incorporated by reference herein in its entirety. In embodiments, the silver nanoparticles can be prepared by a process comprising reacting a silver compound with a reducing agent comprising a hydrazine compound in the presence of a thermally removable stabilizer in a reaction mixture comprising the silver compound, the reducing agent, the stabilizer, and an optional solvent, to form a plurality of silver-containing nanoparticles with molecules of the stabilizer on the surface of the silver-containing nanoparticles. For further detail, see U.S. Pat. No. 7,270,694.
The silver nanoparticles can comprise a silver nanoparticle composition comprising solvents with specific Hansen solubility parameters as described in U.S. Pat. No. 8,765,025, which is hereby incorporated by reference herein in its entirety. In embodiments, the metal nanoparticle composition includes an organic-stabilized metal nanoparticle and a solvent in which the solvent selected has the following Hansen solubility parameters: a dispersion parameter of about 16 MPa0.5, or more, and a sum of a polarity parameter and a hydrogen bonding parameter of about 8.0 MPa0.5 or less. The metal nanoparticle composition is suitable for printing conductive lines that are uniform, smooth and narrow on various substrate surfaces. The metal nanoparticle composition is able to form printed conductive features having a coffee ring effect ratio of about 1.2 to about 0.8, a surface roughness of about 15 or less and a line width of about 200 microns or less. In embodiments, the metal nanoparticle is a silver nanoparticle having a stabilizer associated with a surface of the silver nanoparticle. The silver nanoparticle can, in embodiments, be selected from the group consisting of silver, silver-copper composite, silver-gold-copper composite, silver-gold-palladium composite, and combinations thereof. In embodiments, the stabilizer is an organoamine stabilizer. In embodiments, the organoamine stabilizer can be selected from the group consisting of nonylamine, decylamine, hexadecylamine, undecylamine, dodecylamine, tridecylamine, tetradecylamine, and combinations thereof. In certain embodiments, the silver nanoparticle is one having a stabilizer associated with a surface of the silver nanoparticle, the stabilizer consisting of an organoamine stabilizer, and a solvent, wherein the organoamine stabilizer is a primary alkylamine having at least 9 carbon atoms, wherein the solvent is one or more of decahydronaphthalene, cis-decahydronaphthalene and trans-decahydronaphthalene, and wherein a silver content in the silver nanoparticle is form about 80 weight percent to about 95 weight percent based on the total weight of the silver nanoparticle and the organoamine stabilizer. For further detail, see U.S. Pat. No. 8,765,025.
The silver nanoparticles can be present in the ink composition in any suitable or desired amount. In embodiments, the silver nanoparticles can be present in the ink in an amount of from about 35 to about 80 percent, or from about 40 to about 75 percent, or from about 50 to about 70 percent, based on the total weight of the ink composition.
The silver nanoparticles can be included in the ink composition in the form of a silver concentrate. The silver concentrate can comprise the selected silver nanoparticles and a solvent. The solvent can be selected from any suitable or desired solvent that can form the silver concentrate and be compatible with the other ink components. In embodiments, the silver concentrate solvent can be selected from the group consisting of decalin, bicyclohexane, tetralin, ISOPAR® (refined mineral spirits solvents available from Exxon), xylene, N,N-dimethylaniline, hexadecane, toluene, tetradecane, methyl naphthalene, tetrahydronaphthalene, tetramethyl benzene, ethyl benzene, and the like, and mixtures and combinations thereof. The silver concentrate can be formed by combining the solvent and the silver nanoparticles, optionally in a high speed mixer, stirring, optionally while maintaining the temperature at about 20° C. such as with cold water through a jacketed beaker, optionally with bubbling nitrogen through the dispersion. The silver nanoparticles can optionally be added in the form of a premade silver nanoparticle. In embodiments, the silver nanoparticle can be prepared as described in U.S. Pat. No. 8,765,025 or U.S. patent application Ser. No. 13/866,704, each of which are hereby incorporated by reference herein in their entireties.
Clay Dispersion. The ink composition herein includes a clay dispersion. The clay dispersion comprises clay, a clay dispersant, and a dispersion vehicle. The clay dispersion can be present in the ink composition at any suitable or desired amount. In embodiments, the clay dispersion is provided in the ink composition in an amount of from about 3 to about 50, or from about 4 to about 40, or from about 5 to about 30 percent by weight based on the total weight of the ink composition. It has been discovered that adding about 11.5 weight percent of clay dispersion to the nanosilver ink composition increased the ink viscosity by over 70 percent.
Any suitable or desired clay can be selected for the clay dispersion. In embodiments, the clay comprises an organoclay. In embodiments, the clay can be selected from the group consisting of montmorillonite, modified montmorillonite, and mixtures and combinations thereof. In certain embodiments, the clay selected is a modified montmorillonite designed for use in low to medium polarity printing inks. A specific example of a suitable clay is Claytone® HY commercially available from Southern Clay Products. The clay is added to the nanosilver ink composition to increase ink viscosity. It was surprisingly found that adding clay without any modifications does not increase ink viscosity. In the present embodiments, it was found that the clay needed to be dispersed in order to impact ink viscosity.
The clay can be present in the clay dispersion in any suitable or desired amount. In embodiments, the clay can be present in the clay dispersion in an amount of from about 3 to about 20 percent, or from about 5 to about 15 percent, or from about 6 to about 10 percent clay, based on the total weight of the clay dispersion.
The clay dispersant can comprise any suitable or desired dispersant. In embodiments, the clay dispersant can be selected from the group consisting of polyesters, polyester-amides, polyurethanes, and mixtures and combinations thereof. The dispersant can optionally be a polymeric dispersant, such as a polyester, such as those sold under the name Solsperse®, in embodiments, Solsperse® 1700, Solsperse® 32000, Solsperse® 13240, or Solsperse® J-180 available from The Lubrizol Corporation.
The dispersant can be provided in any suitable or desired amount. In embodiments, the dispersant can be present in an amount of from about 0.5 to about 10 percent, or from about 0.75 to about 5 percent, or from about 1 to about 3 percent total dispersant, based on the total weight of the clay dispersion.
The clay dispersion can optionally further comprise a synergist. Any suitable or desired synergist can be employed.
The clay dispersion further comprises a dispersion vehicle. Any suitable or desired vehicle can be selected. In embodiments, the clay dispersion vehicle can be a solvent, such as a material selected from the group consisting of decalin, bicyclohexane, tetralin, ISOPAR® (refined mineral spirits solvents available from Exxon), xylene, hexadecane, toluene, tetradecane, methyl naphthalene, tetrahydronaphthalene, tetramethyl benzene, ethyl benzene, and the like, and mixtures and combinations thereof.
The clay dispersion vehicle can be provided in any suitable or desired amount. In embodiments, the clay dispersion vehicle can be present in an amount of from about 60 to about 95 percent, or from about 70 to about 93 percent, or from about 75 to about 90 percent total vehicle, based on the total weight of the clay dispersion.
Ink Vehicle. The ink composition herein comprises an ink vehicle. Any suitable or desired ink vehicle can be selected. In embodiments, the ink vehicle can include a solvent, such as a non-polar organic solvent. The solvent can be used as a vehicle for dispersion of the silver nanoparticles to minimize or prevent the silver nanoparticles from agglomerating and/or optionally providing or enhancing the solubility or dispersibility of silver nanoparticles.
Any suitable or desired solvent can be selected. In embodiments, the solvent can be a non-polar organic solvent selected from the group consisting of hydrocarbons such as alkanes, alkenes, alcohols having from about 7 to about 18 carbon atoms such as undecane, dodecane, tridecane, tetradecane, hexadecane, 1-undecanol, 2-undecanol, 3-undecanol, 4-undecanol, 5-undecanol, 6-undecanol, 1-dodecanol, 2-dodecanol, 3-dedecanol, 4-dedecanol, 5-dodecanol, 6-dodecanol, 1-tridecanol, 2-tridecanol, 3-tridecanol, 4-tridecanol, 5-tridecanol, 6-tridecanol, 7-tridecanol, 1-tetradecanol, 2-tetradecanol, 3-tetradecanol, 4-tetradecanol, 5-tetradecanol, 6-tetradecanol, 7-tetradecanol, and the like; alcohols such as terpineol (α-terpineol), β-terpineol, geraniol, cineol, cedral, linalool, 4-terpineol, 3,7-dimethylocta-2,6-dien-lol, 2-(2-propyl)-5-methyl-cyclohexane-1-ol; isoparaffinic hydrocarbons such as isodecane, isododecane; commercially available mixtures of isoparaffins such as Isopar™ E, Isopar™ G, Isopar™ H, Isopar™ L, Isopar™ V, Isopar™ G, manufactured by Exxon Chemical Company; Shellsol® manufactured by Shell Chemical Company; Soltrol® manufactured by Chevron Phillips Chemical Company; Begasol® manufactured by Mobil Petroleum Co., Inc.; IP Solvent 2835 manufactured by Idemitsu Petrochemical CO., Ltd; naphthenic oils; aromatic solvents such as benzene, nitrobenzene, toluene, ortho-, meta-, and para-xylene, and mixtures thereof; 1,3,5-trimethylbenzene (mesitylene); 1,2-, 1,3-, and 1,4-dichlorobenzene and mixtures thereof, trichlorobenzene; cyanobenzene; phenylcyclohexane and tetralin; aliphatic solvents such as isooctane, nonane, decane, dodecane; cyclic aliphatic solvents such as dicyclohexyl and decalin; and mixtures and combinations thereof.
In embodiments, two or more solvents can be used.
The ink vehicle can be present in the ink composition in any suitable or desired amount. In embodiments, the ink vehicle is present in an amount of from about 5 to about 50 weight percent, or from about 10 to about 40 weight percent, or from about 10 to about 30 weight percent, based on the total weight of the nanosilver ink composition.
In embodiments, the ink composition is a high-viscosity composition. In embodiments, the ink disclosed herein has a viscosity of from about 8 to about 100, or from about 10 to about 80, or from about 15 to about 60 centipoise at a temperature of about 25° C. In embodiments, the ink has a viscosity of from about 15 to about 60 centipoise at a temperature in the range of from about 20 to about 30° C.
The nanosilver ink compositions can be prepared by any suitable or desired method. In embodiments, the nanosilver ink compositions can be prepared by combining silver nanoparticles; a clay dispersion; and an ink vehicle, as described herein, with optional stirring, optionally with roll milling.
The fabrication of conductive features, such as an electrically conductive element, from the nanosilver ink composition can be carried out by depositing the composition on a substrate using any suitable deposition technique including flexographic and gravure printing processes at any suitable time prior to or subsequent to the formation of other optional layer or layers on the substrate. Thus deposition of the nanosilver ink composition on the substrate can occur either on a substrate or on a substrate already containing layered material, for example, a semiconductor layer and/or an insulating layer.
The substrate upon which the metal features are deposited may be any suitable substrate including silicon, glass plate, plastic film, sheet, fabric, or paper. For structurally flexible devices, plastic substrates such as polyester, polycarbonate, polyimide sheets, and the like, may be used. The thickness of the substrate can be any suitable thickness such as about 10 micrometers to over 10 millimeters with an exemplary thickness being from about 50 micrometers to about 2 millimeters, especially for a flexible plastic substrate, and from about 0.4 to about 10 millimeters for a rigid substrate such as glass or silicon.
Heating the deposited nanosilver ink composition can be to any suitable or desire temperature, such as to from about 70° C. to about 200° C., or any temperature sufficient to induce the metal nanoparticles to “anneal” and thus form an electrically conductive layer which is suitable for use as an electrically conductive element in electronic devices. The heating temperature is one that does not cause adverse changes in the properties of previously deposited layers or the substrate. In embodiments, use of low heating temperatures allows use of low cost plastic substrates which have an annealing temperature of below 200° C.
The heating can be for any suitable or desire time, such as from about 0.01 second to about 10 hours. The heating can be performed in air, in an inert atmosphere, for example under nitrogen or argon, or in a reducing atmosphere, for example, under nitrogen containing from about 1 to about 20 percent by volume hydrogen. The heating can also be performed under normal atmospheric pressure or at a reduced pressure of, for example, about 1000 mbars to about 0.01 mbars.
Heating encompasses any technique that can impart sufficient energy to the heated material or substrate to (1) anneal the metal nanoparticles and/or (2) remove the optional stabilizer from the metal nanoparticles. Examples of heating techniques include thermal heating (for example, at hot plate, an oven, and a burner), infra-red (“IR”) radiation, laser beam, flash light, microwave radiation, or ultraviolet (“UV”) radiation, or a combination thereof.
In embodiments, after heating, the resulting electrically conductive line has a thickness ranging from about 0.1 to about 20 micrometers, or from about 0.15 to about 10 micrometers. In certain embodiments, after heating, the resulting electrically conductive line has a thickness of from about 0.25 to about 5 micrometers.
The conductivity of the resulting metal element produced by heating the deposited nanosilver ink composition is, for example, more than about 100 Siemens/centimeter (S/cm), more than about 1,000 S/cm, more than about 2,000 S/cm, more than about 5,000 S/cm, more than about 10,000 S/cm, or more than about 50,000 S/cm.
The resulting elements can be used for any suitable or desired application, such as for electrodes, conductive pads, interconnects, conductive lines, conductive tracks, and the like, in electronic devices such as thin film transistors, organic light emitting diodes, RFID tags, photovoltaic, displays, printed antenna, and other electronic devise which required conductive elements or components.
The following Examples are being submitted to further define various species of the present disclosure. These Examples are intended to be illustrative only and are not intended to limit the scope of the present disclosure. Also, parts and percentages are by weight unless otherwise indicated.
Preparation of Silver Concentrate. To a jacketed beaker was added decalin (35 grams) (Evonik Industries) and then stirred with a high speed mixer at 2000 RPM. To this was added silver nano paste (200 grams) (91.32% Ash, prepared according to the procedure described in U.S. Pat. No. 7,270,694, which is hereby incorporated by reference herein in its entirety), over 5 minutes allowing the paste to be dispersed by the mixer. After the addition the dispersion was maintained at 20° C. with cold water through the jacketed beaker while bubbling nitrogen through the dispersion. After 6 hours the concentrate was poured into a glass bottle to afford 175 grams of silver concentrate having 78.26% silver content.
Preparation of Silver Concentrate. To a jacketed beaker was added decalin (35 grams) (Evonik Industries) and then stirred with a high speed mixer at 2000 RPM. To this was added silver nano paste (200 grams) (92.37% Ash, prepared according to the procedure described in U.S. Pat. No. 7,270,694), over 5 minutes allowing the paste to be dispersed by the mixer. After the addition the dispersion was maintained at 20° C. with cold water through the jacketed beaker while bubbling nitrogen through the dispersion. After 6 hours the concentrate was poured into a glass bottle to afford 175 grams of silver concentrate have 78.37% silver content.
Preparation of Clay Dispersion 1. Into a clean 30 milliliter bottle were added the following: 0.161 grams Solsperse® J-180 from The Lubrizol Corporation, 7.26 grams decalin (99.6% purity) from Evonik Industries and the bottle was placed on a jar mill and rotated slowly to effect solution. Into the 30 milliliter bottle were placed 70.0 grams ⅛ inch diameter Grade 1000 440C stainless steel shot from Hoover Precision Products and 0.806 gram Claytone® HY from Southern Clay Products, the latter of which were added slowly while gently swirling the bottle to encourage wetting of the clay. After addition of all the clay, the 30 milliliter bottle containing the clay pre-dispersion was placed on a jar mill and milled slowly at about 30 RPM for 30 minutes to give Clay Dispersion 1.
Preparation of Clay Dispersion 2. Into a clean 30 milliliter bottle were added the following: 0.161 grams Solsperse® 17000 polymeric dispersant from The Lubrizol Corporation, 7.26 grams decalin (99.6% purity) from Evonik Industries and the bottle was placed on a jar mill and rotated slowly to effect solution. Into the 30 milliliter bottle were placed 70.0 grams ⅛ inch diameter Grade 1000 440C stainless steel shot from Hoover Precision Products and 0.806 gram Claytone® HY from Southern Clay Products, the latter of which were added slowly while gently swirling the bottle to encourage wetting of the clay. After addition of all the clay, the 30 milliliter bottle containing the clay pre-dispersion was placed on a jar mill and milled slowly at about 30 RPM for 30 minutes to give Clay Dispersion 2.
Preparation of Ink Example 1. To a 30 milliliter plastic bottle was added 12.446 grams of silver concentrate from Example 1B. This was followed by decalin solvent (1.907 grams) (Evonik Industries) and bicyclohexyl solvent (0.689 grams) (Solutia, Eastman Chemical Company). Glass beads (6.01 grams) were added to the mixture. The sample was purged with argon, tightly sealed using 3M 764 vinyl green tape and roll-milled at 175 RPM for 2 hours. Ink rheology was measured using Ares G2 Rheometer from TA Instruments using a 50 millimeter cone, 0.053 gap. A rate sweep was run from 400 to 4 S−1 at 25° C. Table 1 below shows ink formulation and Table 2 shows ink properties.
Preparation of Ink Example 2. To a 30 milliliter plastic bottle was added 10.80 grams of silver concentrate from Example 1A. This was followed by decalin solvent (1.540 grams) (Evonik Industries), bicyclohexyl solvent (0.544 grams) (Solutia, Eastman Chemical Company) and Claytone® HY clay (0.130 grams). Glass beads (6.20 grams) were added to the mixture. The sample was purged with argon, tightly sealed using 3M 764 vinyl green tape and roll-milled at 175 RPM for 2 hours. Ink rheology was measured using Ares G2 Rheometer from TA instruments using a 50 millimeter cone, 0.053 gap. A rate sweep was run from 400 to 4 S−1 at 25° C. Table 1 below shows ink formulation and Table 2 shows ink properties.
Preparation of Ink Example 3. To a 30 milliliter plastic bottle was added 12.465 grams of silver concentrate from Example 1B. This was followed by Claytone® HY Clay Dispersion 1 from Example 2 (1.061 grams), decalin solvent (0.865 grams) (Evonik Industries) and bicyclohexyl solvent (0.652 grams) (Solutia, Eastman Chemical Company). Glass beads (6.20 grams) were added to the mixture. The sample was purged with argon, tightly sealed using 3M 764 vinyl green tape and roll-milled at 175 RPM for 2 hours. Ink rheology was measured using Ares G2 Rheometer from TA Instruments using a 50 millimeter cone, 0.053 gap. A rate sweep was run from 400 to 4 S−1 at 25° C. Table 1 below shows ink formulation and Table 2 shows ink properties.
Preparation of Ink Example 4. Ink Example 4 was prepared in the same way as Ink Example 3 (Example 6) except that Claytone® HY Clay Dispersion 2 from Example 3 was used.
Preparation of Ink Example 5. Ink Example 5 was prepared in the same way as Ink Example 3 (Example 6) except that Claytone® HY Clay Dispersion 2 from Example 3 was used.
AOP meaning Additive on Pigment.
The viscosity data were obtained at 25° C. on an Ares G2 Rheometer from TA Instruments using a 50 millimeter cone, 0.053 gap. A rate sweep was run from 1000 to 4 S−1.
Viscosities of ink Examples 1 and 2 are similar although ink Example 2 comprised 1 weight percent clay. Adding unprocessed clay to the ink did not increase the ink viscosity. Clay dispersions prepared by dispersing clay in Solsperse® J-180 and Solsperse® 17000 and adding the clay concentrates to the ink increased viscosities as shown in Table 2. As the amount of clay concentrate increases, viscosity increases. Viscosity profiles of ink Example 1 (Control), Example 4, and Example 5 are shown in
Ink examples 1, 4, and 5 were printed using a Flexi-proof printer (RK Printcoat Instruments, Royston, UK) having a design as shown in
Resistance measurements on the conductivity lines shown in
Resistivity is an average of the 50, 100, 600 and 1,000 micrometer line (measured the 2 lines on each side) and 2 prints were assessed. Bulk silver conductivity is the bulk silver conductivity (6.3×105 s/cm) divided by the sample conductivity. A very conductive sample will give a value of 1. The printed films were still conductive indicating that the clay was not negatively impacting ink performance. Adding the clay concentrate decreased conductivity but not as much as has been observed with other additives. Other polymer additives depress conductivity by 2 orders of magnitude. The bulk conductivity of the control Ink Example 1 was 2.27×bulk silver and that of the ink Examples 5 of the of the present disclosure was 7.25×bulk silver. A bulk silver conductivity ratio of less than 10 is acceptable. In embodiments, the ink herein has a bulk conductivity that is more than about 50,000 S/cm. Thus, a novel nanosilver ink composition is provided comprising clay additives in the form of clay dispersions. The inks have higher viscosity than the control ink. The inks have been shown to have better printability by flexography and are expected to show improved gravure printability as well. The printed images have acceptable conductivity.
It will be appreciated that various of the above-disclosed and other features and functions, or alternatives thereof, may be desirably combined into many other different systems or applications. Also that various presently unforeseen or unanticipated alternatives, modifications, variations or improvements therein may be subsequently made by those skilled in the art which are also intended to be encompassed by the following claims. Unless specifically recited in a claim, steps or components of claims should not be implied or imported from the specification or any other claims as to any particular order, number, position, size, shape, angle, color, or material.
