Patent Application
20070116904
Inkjet printing has become a popular way of recording images on various media surfaces, particularly paper, for a number of reasons, including, low printer noise, capability of high-speed recording, and multi-color recording. Additionally, these advantages of inkjet printing can be obtained at a relatively low price to consumers. Though there has been great improvement in inkjet printing, improvements are followed by increased demands from consumers for higher speeds, higher resolution, full color image formation, increased stability, etc.
In recent years, as digital cameras and other digital image collecting devices have advanced, image recording technology has attempted to keep pace by improving inkjet image recording on paper sheets and the like. The desired quality level of the inkjet recorded images (“hard copy”) is that of traditional silver halide photography. In other words, consumers would like inkjet recorded images that have the color reproduction, image density, gloss, etc. that is as close to those of silver halide photography as possible.
Traditional recording sheets for the inkjet printing process are not adequate to provide silver halide quality images. Particularly, there is a need to improve ink absorption capacity, ink absorption rate or dry time, image quality, and gloss.
In one aspect of the present system and method, an ink receiving substrate includes a base substrate and a microporous coating formed on the base substrate. The microporous coating includes a high surface area fumed alumina and a high molecular weight polyvinyl alcohol binder.
In another embodiment, a method for forming an ink receiving substrate includes providing a base substrate, combining a high surface area fumed alumina with a high molecular weight polyvinyl alcohol binder to form a coating, and dispensing a layer of the coating on at least one surface of the base substrate.
The accompanying drawings illustrate various embodiments of the present system and method and are a part of the specification. The illustrated embodiments are merely examples of the present system and method and do not limit the scope thereof.
Throughout the drawings, identical reference numbers designate similar, but not necessarily identical, elements.
The present specification discloses an exemplary microporous ink recording material having improved ink dry time, gloss, and capacity compared to microporous ink recording materials incorporating low surface area fumed alumina materials. According to one exemplary embodiment disclosed herein, the microporous ink recording material includes a layer of high surface area fumed alumina such as VP Alu 3. Further details of the present ink recording material will be provided below.
Before particular embodiments of the present system and method are disclosed and described, it is to be understood that the present system and method are not limited to the particular process and materials disclosed herein as such may vary to some degree. It is also to be understood that the terminology used herein is used for the purpose of describing particular embodiments only and is not intended to be limiting, as the scope of the present system and method will be defined only by the appended claims and equivalents thereof.
As used in the present specification and in the appended claims, the term “ink” is defined to include liquid compositions that can include colorants, such as pigments and/or dyes, as well as liquid vehicles configured to carry the colorants to a substrate. Liquid vehicles are well known in the art, and a wide variety of liquid vehicle components may be used in accordance with embodiments of the present exemplary system and method. Such liquid vehicles may include a mixture of a variety of different agents, including without limitation, surfactants, co-solvents, buffers, biocides, viscosity modifiers, sequestering agents, stabilizing agents, and water. Though not liquid per se, the liquid vehicle can also carry other solids, such as polymers, UV curable materials, plasticizers, salts, etc.
Concentrations, 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 range of approximately 1 wt % to about 20 wt % should be interpreted to include not only the explicitly recited concentration limits of 1 wt % to about 20 wt %, but also to include individual concentrations such as 2 wt %, 3 wt %, 4 wt %, and sub-ranges such as 5 wt % to 15 wt %, 10 wt % to 20 wt %, etc.
As used in the present specification and the appended claims, the term “high surface area fumed alumina” is meant to be understood as including any fumed alumina particles having a surface area greater than approximately 110 m2 per gram.
Additionally, as used herein, the term “high molecular weight polyvinyl alcohol binder” or “high molecular weight PVA binder” shall be interpreted as including any polyvinyl alcohol based binder having a molar mass of 300,000 grams per mol or more. According to one exemplary embodiment, high molecular weight polyvinyl alcohol binders shall be interpreted as including, but not being limited to, Poval 235 and Poval 245, manufactured by Kuraray America, Inc.
In the following description, for purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the present system and method for producing an exemplary microporous ink recording material having improved ink dry time, gloss, and ink capacity. It will be apparent, however, to one skilled in the art, that the present method may be practiced without these specific details. Reference in the specification to “one embodiment” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment. The appearance of the phrase “in one embodiment” in various places in the specification are not necessarily all referring to the same embodiment.
Exemplary Structure
The computing device (110) that is controllably coupled to the servo mechanism (120), as shown in
The moveable carriage (140) of the present printing system (100) illustrated in
As an image or text is printed on the ink receiving structure (170), the computing device (110) may controllably position the moveable carriage (140) and direct one or more of the inkjet dispensers (150) to selectively dispense an inkjet ink at predetermined locations on the ink receiving structure (170) as digitally addressed drops, thereby forming the desired image or text. The inkjet material dispensers (150) used by the present printing system (100) may be any type of inkjet dispenser configured to perform the present method including, but in no way limited to, thermally actuated inkjet dispensers, mechanically actuated inkjet dispensers, electrostatically actuated inkjet dispensers, magnetically actuated dispensers, piezoelectrically actuated dispensers, continuous inkjet dispensers, etc. Additionally, the present ink receiving structure (170) may receive inks from non-inkjet sources such as, but in no way limited to, screen printing, stamping, pressing, gravure printing, and the like.
The material reservoir (130) that is fluidly coupled to the inkjet material dispenser (150) houses and supplies an inkjet ink (160) to the inkjet material dispenser. The material reservoir may be any container configured to hermetically seal the pigment-based inkjet ink (160) prior to printing.
The present system and methods provide a porous ink receiving structure (170) with enhanced image quality, the composition of which will now be described in detail below.
Exemplary Composition
One exemplary composition of the present exemplary ink receiving structure (170) configured to receive an inkjet ink (160) is illustrated in
Resin Coated Base Paper
The present exemplary ink receiving structure (170) is formed on a resin coated base layer (172) or support. According to one exemplary embodiment, any number of the usual resin coated base supports used in the manufacture of transparent or opaque photographic material may also be employed in the practice of the present system and method. Examples include, but are not limited to, clear films, such a cellulose esters, including cellulose triacetate, cellulose acetate, cellulose propionate, or cellulose acetate butyrate, polyesters, including poly(ethylene terephthalate), polyimides, polycarbonates, polyamides, polyolefins, poly(vinyl acetals), polyethers, polyvinyl chloride, and polysulfonamides. Polyester film supports, and especially poly(ethylene terephthalate), such as manufactured by du Pont de Nemours under the trade designation of MELINEX, may be selected because of their excellent dimensional stability characteristics. Further, opaque photographic materials may be used as the resin coated base layer (172) including, but in no way limited to, baryta paper, polyethylene-coated papers, and voided polyester.
Non-photographic materials, such as transparent films for overhead projectors, may also be used for the support material. Examples of such transparent films include, but are not limited to, polyesters, diacetates, triacetates, polystyrenes, polyethylenes, polycarbonates, polymethacrylates, cellophane, celluloid, polyvinyl chlorides, polyvinylidene chlorides, polysulfones, and polyimides.
While the present exemplary ink receiving structure (170) is described within the context of utilizing a resin coated base layer (172), any number of additional support materials may be used as a base layer by the present exemplary system and method. Additional support materials that may be incorporated by the present system and method to serve as the resin coated base layer (172) include plain paper of various different types, including, but in no way limited to, plain papers, pigmented papers, and cast-coated papers, as well as metal foils, such as foils made from alumina.
High Surface Area Fumed Alumina
As illustrated in
According to one exemplary embodiment, the resin coated base layer (172) is coated with high surface area fumed alumina layer (174). The high surface area fumed alumina is mixed with a high molecular weight PVA binder and then disposed on the resin coated base layer (172). According to this exemplary embodiment, the high surface area fumed alumina may be any fumed alumina having an aggregate size between approximately 100-110 nm. Additionally, according to the present exemplary embodiment, the phrase “high surface area fumed alumina” will be meant to include any fumed alumina having a surface area greater than approximately 110 m2/gram. Commercially available examples of high surface area fumed alumina include, but are in no way limited to, VP Alu 3® powder supplied by Degussa Company.
According to one exemplary embodiment, the use of the high surface area fumed alumina provides higher gloss than traditional fumed silica due to the increased surface area. Specifically, the high surface area fumed alumina generates a higher glossed surface area due to the increased surface area exposed by the resin coated base layer. Additionally, the dry time and ink capacity associated with the high surface area fumed alumina is increased.
However, according to one exemplary embodiment, the high surface area fumed alumina may be more prone to cracking than fumed alumina. Consequently, one exemplary embodiment of the present high surface area fumed alumina layer (174) includes a very high molecular weight polyvinyl alcohol binder. According to one exemplary embodiment, any number of high molecular weight PVA binders may be used in connection with the high surface area fumed alumina including, but in no way limited to, Poval 235 and Poval 245, commercially available from Kuraray, Inc.
According to the present exemplary embodiment, the binder/fumed alumina ratio is from approximately 10 to 40 parts based on the fumed alumina. The incorporation of a high molecular weight PVA binder reduces the likelihood of cracking due to the high surface area of the pigment.
In addition to the above-mentioned components, the high surface area fumed alumina layer (174) may also contain any number of surfactants, buffers, plasticizers, and other additives that are well known in the art. According to one exemplary embodiment, a buffer such as boric acid may be included in quantities of approximately 1.0 to 1.2% wt.
During application, the high surface area fumed alumina layer (174) can be coated onto the resin coated base layer (172) by any number of material dispensing machines and/or methods including, but in no way limited to, a slot coater, a curtain coater, a cascade coater, a blade coater, a rod coater, a gravure coater, a Mylar rod coater, a wired coater, and the like. Further details of the method of formation of the present exemplary high surface area fumed alumina layer will be provided below with reference to
Exemplary Formation
Once the powder is acquired, a dispersant is prepared (step 310). According to one exemplary embodiment, the dispersant may be an acetic acid solution in deionized water. The amount of dispersant used may vary depending on the weight percent of desired solids in the final dispersion. According to one exemplary embodiment targeting approximately 45% wt solids, a 4% wt of acetic acid solution in deionized water may be prepared.
With the high area fumed alumina powder acquired (step 300) and the dispersant prepared (step 310), the next step in the preparation of the high surface area fumed alumina layer (174;
With the alumina powder incorporated into the dispersion, the dispersion is allowed to cool (step 330) to room temperature. Once cooled appropriately, the fumed alumina dispersion may then be combined with a high molecular weight PVA water solution (step 340). According to one exemplary embodiment, the step of combining the high surface area fumed alumina dispersion with the high molecular weight PVA water solution (step 340) includes adding a desired amount of the high molecular weight PVA water solution into the fumed alumina dispersion followed by mixing and the inclusion of appropriate amounts of deionized water and boric acid to maintain a desired solid % wt and pH.
With the high surface area fumed alumina mixture prepared, it may then be applied to a desired resin coated base (step 350). According to one exemplary embodiment, the high surface area fumed alumina mixture may be applied to a desired resin coated base layer (step 350) using any number of known coating techniques including, but in no way limited to, a slot coater, a curtain coater, a cascade coater, a blade coater, a rod coater, a gravure coater, a Mylar rod coater, a wired coater, and the like. Further details and examples of the present exemplary high surface area fumed alumina mixture, as well as its performance compared to traditional coating will be provided below.
According to a first exemplary embodiment, a plurality of coating mixtures were produced using the exemplary method illustrated in
A first mixture was generated using VP Alu 3® powder from Degussa Company as a high surface area fumed alumina example. The dispersion prepared for the study targeted 45% wt as final solids using 4% wt of Acetic Acid solution in D.I. Water as dispersant. The preparation of dispersion was done by mixing the VP Alu 3® powder into the dispersant using partially baffled mixing tank and a Rushton turbine (6 blades turbine of θ=1.5″). The rotational speed was set to allow good visible vertical circulation and varied from approximately 650 rpm at the beginning to approximately 4,000 rpm at the end of the process. After all of the powder was incorporated into dispersion the mixing process was allowed for additional 20 minutes and the samples for the actual solids content and particles size distribution were taken. Finally, the dispersion was allowed to sit for approximately 2 hours to allow it to cool down to room temperature and viscosity and pH measurements were taken. At this point the dispersion was ready for use in the preparation of the coating mixtures (the lacquers).
With the dispersion prepared, the lacquers (coating mixtures) were generated by adding the desired amount of PVA's water solution into the dispersion, mixed well followed with adding necessary amount of D.I. water and boric acid while mixing. Lacquers were prepared using both high and low molecular weight PVA binders. Each mixture was stirred for additional 5-10 minutes, sampled for solids, particle size and aged over night and sampled for viscosity and pH before coating.
Similarly, a second mixture was prepared using AluC® from the Degussa Company as a standard fumed alumina example. Two different dispersions were prepared for the study: 1) A20 and 2) A40. Both dispersions are targeted 45% wt as final solids using 2% wt and 4% wt of Acetic Acid solutions in D.I. Water respectively as dispersant. The preparation of dispersions were done by mixing the AluC® powder into the dispersant using partially baffled mixing tank and a Rushton turbine (6 blades turbine of θ=1.5″). The rotational speed was set to allow good visible vertical circulation and varied from approximately 650 rpm at the beginning to approximately 1,800 rpm at the end of the process. After all of the powder was incorporated into dispersion the mixing process was allowed for additional 20 minutes and the samples for the actual solids content and particles size distribution were taken. Finally, the dispersion was allowed to sit for approximately 2 hours to allow it to cool down to room temperature and the measurement for viscosity and pH was taken. At this point the dispersion was ready for use in the preparation of the coating mixtures (the lacquers).
The coating mixtures (the lacquers) were prepared by adding the desired amount of PVA water solution into the A20 or A40 dispersion, mixed well followed with adding necessary amount of D.I. water and boric acid while mixing. Again, both high density and low density PVA binders were used in various lacquer mixtures. Each mixture was stirred for additional 5-10 minutes, sampled for solids, particle size and let aged over night and sampled for viscosity and pH before coating.
With the experimental coatings prepared, the coatings were applied on a resin coated paper. Five sheets were coated of each lacquer with the targeted 35 gsm and dried at 60° C. in a convection oven with air flow. The dry sheets were cut to 11″×8.5″ size and evaluated for: a) water capacity; b) gloss (at 20o, 60o and 85o); c) smudge drying time; d) coalescence; e) gamut and f) cracks.
According to the above-mentioned experiment, both the high surface area fumed alumina (VP Alu 3®)) and the low surface area fumed alumina (AluC®) produced Mercedes cracks when coated with the lower molecular weight PVA binder. However, when combined with the higher molecular weight PVA binder, the cracks were not present for either the high surface area fumed alumina (VP Alu 3®) or the low surface area fumed alumina (AluC®). However, when combined with the high molecular weight PVA binder, the coating incorporating the high surface area fumed alumina (VP Alu 3®) exhibited higher relative capacity, lower smudge drying time, lower coalescence, higher gamut and gloss properties than the coating incorporating the low surface area fumed alumina (AluC®).
In conclusion, the above-mentioned example illustrates a number of benefits that may be provided by the present exemplary system and method, according to one exemplary embodiment. More specifically, the exemplary microporous ink recording material incorporating a layer of high surface area fumed alumina in combination with a high molecular weight binder generates improved ink dry time, gloss, and capacity compared to low surface area fumed alumina.
The preceding description has been presented only to illustrate and describe exemplary embodiments of the present system and method. It is not intended to be exhaustive or to limit the system and method to any precise form disclosed. Many modifications and variations are possible in light of the above teaching. It is intended that the scope of the system and method be defined by the following claims.
