Patent Application
20080078304
The composition of the present invention comprises a liquid vehicle and a water soluble alkylated or hydroxyalkylated branched polyethyleneimine. Prior to alkylation or hydroxyalkylation, branched polyethyleneimines comprise a combination of primary, secondary and tertiary amino groups, typically in a molar ratio of approximately 1:2:1. In accordance with the invention, at least 1% of the primary amino groups of the branched polyethyleneimine polymer are alkylated or hydroxyalkylated with at least one alkyl or hydroxyalkyl group having 4-6 carbon atoms. In a preferred embodiment, at least 3 mole percent of the substitutable hydrogens of the primary and secondary amino groups of the branched polyethyleneimine are alkylated or hydroxyalkylated with alkyl or hydroxyalkyl groups having 4-6 carbon atoms. Specific examples of such compounds include hydroxybutylated PEI, and hexylated-PEI.
When employing alkyl groups having 4-6 carbon atoms, to maintain adequate solubility it is preferred that only 1-10 mole percent of the substitutable hydrogens of the amino groups of the branched polyethyleneimine are alkylated with such alkyl groups. In such case, in a further preferred embodiment at least 5 percent of the remaining substitutable hydrogens of the amino groups of the branched polyethyleneimine may be hydroxyalkylated with hydroxyalkyl groups having 1-3 carbon atoms. In a specific preferred embodiment, 1-10 mole percent of the substitutable hydrogens of the amino groups of the branched polyethyleneimine may be alkylated with hexyl groups and any amino groups of the branched polyethyleneimine having remaining substitutable hydrogens may be fully hydroxyethylated.
When employing hydroxyalkyl groups having 4-6 carbon atoms, they may be employed at any mole percent of the hydroxyalkyl groups having 4-6 carbon atoms wherein water solubility is maintained. In a specific embodiment, the amino groups of the branched polyethyleneimine having substitutable hydrogens may be fully hydroxybutylated. In an alternative embodiment, hydroxyalkyl groups having 4-6 carbon atoms may be employed to hydroxyalkylate a first portion of the amino groups of the branched polyethyleneimine having substitutable hydrogens, and hydroxyalkyl groups having 1-3 carbon atoms may be employed to hydroxyalkylate a second portion of the amino groups of the branched polyethyleneimine, up to a fully alkoxylated position.
Alkylated, hydroxyalkylated, and alkylated/hydroxyalkylated branched polyethyleneimine polymers employed in the present invention may be prepared by alkylating and/or hydroxyalkylating commercially available branched PEI polymers employing conventional alkylation and hydroxyalkylation chemistry.
When employed with anionic water soluble dyes, such specific branched polyethyleneimine polymers comprising such 4-6 carbon atom alkyl and hydroxyalkyl substituents have been found to surprisingly result in increased optical density, as well as providing additionally desired attributes of improved waterfastness. By limiting the length of the alkyl groups, and or the amount of substitution with such specific substituents, the solubility of the PEI derivatives may be controlled so as also not to be substantially detrimentally altered as compared to the unsubstituted derivatives.
Branched polyethyleneimine polymers employed in accordance with the invention typically will have a molecular weight range of approximately 10,000 to 60,000, although lower or higher molecular weight polymers may also be useful.
By incorporating an anionic dye soluble in the liquid vehicle, compositions in accordance with the invention may provide waterfast, dye-based ink that is suitable for inkjet printing. The use of a dye based ink is preferable in compositions of the invention, as the viscosity of the solutions allows for runnability in a CIJ printing system. The dye in the ink jet ink composition of such embodiment of the present invention is water soluble and preferably selected from the group consisting of Direct Dyes, Acid Dyes, and Food Dyes. For ink jet ink compositions, the water soluble branched polyethyeleneimine polymer is preferably present in an amount of from about 0.5 to 5.0% by dry weight basis, and the anionic dye is preferably present in an amount of from about 1.0 to 5.0% by dry weight basis, more preferably between about 2% and 4% by weight.
While the compositions of the invention may include a dye to form an ink composition, compositions in accordance with the invention without dye incorporated therein are also useful, and may be employed, e.g., to be coated or printed on a substrate either before or after printing of a dye composition in order to improve the properties of the printed dye. In accordance with a further embodiment, the present invention is accordingly also directed towards a medium for printing an ink jet image on, comprising a substrate and a surface layer comprising an alkylated or hydroxyalkylated branched polyethyleneimine coated from a composition in accordance with the present invention.
It is understood and known in the art that waterfastness is substrate dependent. The composition of the present invention is particularly adaptable for incorporation into an ink jet printing apparatus for forming images by causing the ink to be expelled as droplets onto a substrate, thereby generating an image on a wide variety of substrates. Additionally, the present invention allows for the addition of other chemicals necessary for particular substrates. For example, when necessitated, a surfactant may be added when high gloss substrates are used.
It will be appreciated that while inclusion of a PEI polymer increases waterfastness, there may also be premature interaction between the anionic dye and the cationic PEI while within the drop generator. Thus, it is preferred to prevent this interaction until it becomes desirable. In a further aspect of such embodiment, a dimethylaminoethanol (“DMAE”) base may be included in an amount sufficient to provide a pH of above 10 to reduce the cationic charge on the polymer to a minimum and discourage electrostatic interactions between the polyethyleneimine and the dye. After jetting, the DMAE evaporates, reducing the pH and allowing the PEI and dye to interact and create a waterfast ink.
In some systems, it may be anticipated that other chemicals may be required for proper application of the present ink formulation. For example, defoamers, biocides to reduce bacterial growth, anticorrosion to protect hardware, surfactant which are dependent upon the desired substrate, alcohols, buffers, and etc of which aid in the specialization of the ink formulation for a particular usage. In particular embodiments, e.g., other additives that may optionally be included in the compositions of the invention include a corrosion inhibitor in an amount from 0 to 0.2 wt. % such as an alkanolamino-group; a wetting agent of from 0 to 1 wt. %, such as an ethoxylated glycol ether; a lower aliphatic alcohol having one hydroxy group and up to five carbon atoms in a straight or branched chain in an amount of 0 to 10 wt. %; and a biocide from 0 to 0.5 wt. % such as dehydroacetic acid. The compositions may also include an optional defoamer such as phosphate esters, silicone or non-silicone defoamer or acetylenic diol.
The following synthesis examples are provided as representative of techniques for preparation of alkylated, hydroxyalkylated, and alkylated/hydroxyalkylated branched polyethyleneimine polymers that may be employed in the present invention. As indicated above, such polymers may be prepared by alkylating and/or hydroxyalkylating commercially available branched PEI polymers employing conventional alkylation and hydroxyalkylation chemistry.
18 g of branched polyethyleneimine (PEI) was dissolved in 180 ml of THF. 4.11 ml of hexylbromide was added to the solution, and the reaction refluxed for 48 hours at 75-85 C. After 48 hours, 1.16 g of NaOH was dissolved in MeOH and the solution was added to the reaction as it continued to reflux for 24 hours. Once completed, the reaction was allowed to settle for 24 hours, filtered, and solvent was removed on a rotary evaporator. The resulting yellow sample was dried under vacuum, resulting in 7% hexylated branched polyethyleneimine (7% HPEI).
15 g of 7% hexylated branched polyethyleneimine (7% HPEI) was dissolved in 125 ml of ethanol. 25 ml of rinse, alongside the solution and a bomb container, were allowed to sparge with N2 for 12-15 min. Each was added to the bomb along with 4.09 ml of propylene oxide. The reaction was heated to 60 C (5-7 hours) and then allowed to cool overnight. Once removed from the bomb, the reaction was evaporated for 24 hours and was dissolved in H2O and transferred to 8 k MWCO dialysis tubing for 48 hours. The sample was then dried down to a desired percentage of solid in solution for delivery. GPC MW: 3,260. PDI: 1.944.
15 g of 7% hexylated branched polyethyleneimine (7% HPEI) was dissolved in 125 ml of ethanol. 25 ml of rinse, alongside the solution and a bomb container, were allowed to sparge with N2 for 12-15 min. Each was added to the bomb along with 7.66 ml of propylene oxide. The reaction was heated to 60 C (5-7 hours) and then allowed to cool overnight. Once removed from the bomb, the reaction was evaporated for 24 hours and was dissolved in H2O and transferred to 8 k MWCO dialysis tubing for 48 hours. The sample was then dried down to a desired percentage of solid in solution for delivery. GPC MW: 3,278. PDI: 1.885.
An ink made in accordance with an embodiment of the present invention may be manufactured as follows:
The following preparations provide a comparison of use of alkylated and hydroxyalkylated branched polyethyleneimines in accordance with the invention with a currently used ink formulation, such as the Kodak FD 1096 black ink. Alkylation or hydroxyalkylation in accordance with the current invention provides the benefit of substituted primary and secondary amino-groups without loosing substantial solubility, while also providing greater optical density. In each example, the category of “Other” designates convention biocide, alcohol, glycol, or other additive. In Examples 1-3, the branched PEI employed in each case was fully hydroxyalkylated.
To determine the effectiveness of each solution in each example above, the solutions were applied onto a variety of substrates with a #6 drawn down rod, including Laser MOCR Bond, Sterling Ultra Gloss, Smart Paper Kromekote, IP Carolina Cover C1S, and UPM Digibright/Brite 72. The inked substrates were then evaluated for waterfastness and print intensity. While repeat measurements were taken at 0, 24, and 48 hours, only the initial evaluation results are shown below, as one skilled in the art will appreciate that waterfastness and optical density improve with drying time. The results are summarized below, wherein optical density/waterfastness are provided for each substrate:
As can be determined from the results above, the optical density and waterfastness remain highly dependent upon the selected substrate. The four-carbon hydroxyalkyl-derivative, however, showed the overall best optical density and waterfastness by a significant margin, especially on the coated substrates.
Alkylated PEI derivatives were also prepared with varying degrees of amino-group substitution. For the following examples, 3, 5, and 7% hexylated polyethyleneimine were used.
Example solutions were treated similar to manner described above, and the results include:
Optical density and waterfastness for the hexylated PEI were drastically increased as compared to the standard hydroxyethylated PEI derivative traditionally used in inks. While the percentage of alkylation of the amino-groups made slight differences in the observed values on some substrates, generally, there was a significant increase in the observed values on the coated substrates with increased alkylation.
Partially alkylated and partially hydroxyalkylated PEI derivatives were also prepared with varying degrees of amino-group substitution. For the following examples, 7% hexylated and either 23% or 43% hydroxypropylated polyethyleneimine were used.
Example solutions were treated similar to manner described above, and the average optical density/waterfastness results for coated substrates and uncoated substrates are reported below:
Optical density and waterfastness for the hexylated/hydroxypropylated PEI were drastically increased as compared to results previously reported for the standard hydroxyethylated PEI derivative traditionally used in inks, and even further improved relative to the results for the individually hexylated or hydroxypropylated PEI examples previously reported.
The present invention is useful in the field of ink jet printing, and has the advantage of formulating a modified composition for coating or printing for use in ink jet printing which has increased composition solubility and increased printed ink waterfastness.
The invention has been described in detail with particular reference to certain preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention.
