Patent Application
20070281855
The present invention is an oxidation catalyst system that lends itself to one-step application to a substrate or surface, the choice of which is not a limitation of the present invention. By way of illustrative example, the system described herein can be used in the oxidation of CO back to CO2. However, it will be readily understood by one of ordinary skill in the art that the novel aspects of the present invention can be extended to a wide variety of oxidation (and oxidation/reduction) processes.
In accordance with the present invention, an oxidation catalyst system is created when particles of an oxidation catalyst are dispersed in a sol-gel binder. In the illustrative example, the oxidation catalyst is platinum-coated tin oxide. More specifically, particles of platinum-coated tin oxide are fabricated in a size range that is comparable to the size of pigments used in conventional paint products that can be brushed or sprayed onto a substrate or surface. Accordingly, in this example, the particles of platinum-coated tin oxide (or other suitable catalyst material) have diameters on the order of approximately 10 microns or less.
As would be understood in the art of such particle fabrication, a tin oxide dust is first made by mixing tin metal and nitric acid. One method for coating the tin oxide with platinum is described in U.S. Pat. No. 4,912,082, the contents of which are hereby incorporated by reference. Briefly, the tin oxide dust is mixed with a solution containing a platinum precursor, such as tetraamine platinum (II) hydroxide [Pt(NH3)4(OH)2] dissolved in water, which coats the tin oxide particles. The platinum-coated tin oxide is then heated/sintered, resulting in a conversion of the platinum precursor on the tin oxide to platinum metal. As would be understood in the art of such catalyst formulation, other established methods could also be used. If agglomeration of the platinum-coated tin oxide particles occurs during this heating step, the material is simply re-ground to create small particles suitable for dispersion. Depending on the particular oxidation application, the weight percent of platinum in the platinum-coated tin oxide is typically in the range of 3-20% platinum.
The sol-gel binder in which the oxidation catalyst particles are mixed can be made from any of a variety of precursors that, when processed, form a porous sol-gel network. For example, suitable sol-gel precursors include silica, alumina, zirconia, ceria, vanadia, metal oxides, and mixtures of these precursors. In the illustrative example, an alumina sol-gel binder was prepared for use with the platinum-coated tin oxide oxidation catalyst particles. A detailed description of sol-gel preparation is provided by X. J. Wang et al. in “Phase Trans Formation of Er3−-doped Al2O3 Powders Prepared by the Sol-Gel Method,” J. Mater. Res., Vol. 18, No. 10, 2003, pp. 2401-2405, the contents of which are hereby incorporated by reference. Briefly, an aqueous solution of aluminum isopropoxide was refluxed at 90° C. under vigorous stirring for two hours. After heating, a small amount of nitric acid was added to catalyze the hydrolysis of the alumina and refluxed for an additional 16 hours resulting in the formation of a clear sol.
The above-described platinum-coated tin oxide particles were then mixed with the above-described clear sol. The sizing of the particles as described above provided for their dispersion in the sol-gel binder. In testing various examples of this exemplary formulation, it was found that effective “CO-to-CO2” oxidation resulted when there was approximately 10-20% by weight of the platinum-coated tin oxide particles in the sol-gel mixture. When this mixture turns to a gel, an embodiment of the present invention's oxidation catalyst system is formed.
Prior to gel formation, the mixture of the oxidation catalyst particles in the porous sol-gel binder can be applied in one step by brushing or spraying. If the mixture is too viscous for conventional paint applications or if the mixture gels too quickly, the mixture may need to be “thinned”. That is, the particle-binder mixture (while the binder is in its sol state) can be thinned as necessary for ease of application and/or to retard the “sol-to-gel” conversion of the sol-gel binder. Such thinning is a process well-known in the paint formulation art with the thinner being selected to prevent unwanted reactions with the sol-gel binder and the oxidation catalyst particles. For the illustrated example of alumina sol-gel and platinum-coated tin oxide particles, a suitable thinner is 2-butanone or methyl ethyl ketone (MEK) as it is also known.
Once the above-described oxidation catalyst system in its sol state is coated (e.g., sprayed, brushed, etc.) on a substrate or surface, some drying time is required to allow any excess water to be removed. The coating can also be exposed to low temperature heat (e.g., on the order of 100-110° C. for the illustrated example) to speed up the drying process.
The advantages of the present invention are numerous. The oxidation catalyst system described herein can be applied in one step while the system's binder is in its sol state. Such application involves conventional painting techniques. The system is therefore readily applied to cloth-based filters, flexible substrates, thin screens, etc., using just the amount of material needed to coat the substrate. The sol-gel binder provides for (i) mechanical stabilization of the oxidation catalyst particles within the porous structure of the sol-gel binder, (ii) adhesion of the “system” to a substrate, and (iii) catalytic conversion of CO to CO2 and water owing to the porous nature of the sol-gel binder. Tests of the present invention yielded effective catalytic reactions.
Although the invention has been described relative to a specific embodiment thereof, there are numerous variations and modifications that will be readily apparent to those skilled in the art in light of the above teachings. It is therefore to be understood that, within the scope of the appended claims, the invention may be practiced other than as specifically described.
The invention was made in part by employees of the United States Government and may be manufactured and used by or for the Government of the United States of America for governmental purposes without the payment of any royalties thereon or therefor.
