Patent Application
20070110919
The invention relates to a method of producing photocatalytically active coatings on polymers in a cold-gas spraying process, wherein powder particles of the photocatalytically active material are accelerated in a carrier gas to speeds of up to 1,500 m/s and upon impact penetrate into the surface of the polymer to a depth of several micrometers to form a mechanically firmly adhering laminar structure with the polymer. The carrier gas is relaxed at an output pressure of up to 6.3 MPa and an output temperature of up to 800° C. in a supersonic nozzle or sonic nozzle and in the process is accelerated to speeds of up to 1,500 m/s.
It is known to apply coatings to substrates of many different types by means of various methods. Investigations are described in the literature where photocatalytically active coatings are produced by different methods. See, e.g., German Patent No. DE 10119288, U.S. Patent Application No. 2002/0168466 and H. Ohsaki et al., Plasma Treatment for Crystallization of Amorphous Thin Films, Proceed. 5th ICCG, Saarbrücken, 2004. Plasma spraying has been disclosed in articles by F. X. Ye et al., Investigation of the Photocatalytic Efficiencies of Plasma Sprayed TiO2—Fe2O3 Coatings (S. 169-174) and by N. Berger-Keller et al., Influence of Plasma Spray Parameters on Microstructural Characteristics of TiO2 Deposits (S. 1403-1408), both of which appeared in Thermal Spray 2003: Advancing the Science & Applying the Technology, C. Moreau and B. Marple (Eds.), ASM International Materials Park, Ohio (2003). Chemical vapor deposition (CVD) of photocatalytically active coatings has been described by S. A. O'Neill et al., Chem. Mater., 15, 46-50 (2003), and the sol-gel coating of photocatalytically active coatings has been described by M. Z. Atashbar, et al., Thin Solid Films, 326, 238-244 (1998). Other deposition methods include high-speed flame spraying (HVOF) and sputtering. It is the object of this work to achieve an optimal method of operation of the photocatalytic layer, for example TiO2, for the respective application by means of targeted process parameters.
It is also known that titanium dioxide occurs in different modifications. In addition to the stable rutile phase, titanium dioxide can also occur in the photocatalytically active anatase phase which, however, irreversibly changes to rutile above the temperature range of from 600-800° C. The titanium dioxide can be produced in different manners as powder in the form of the anatase phase. During conventional thermal spraying of anatase powders, however, this TiO2 phase changes partially or completely to the rutile phase, whereby the photocatalytic characteristics of the produced layer are impaired or lost. This disadvantage can be partially compensated by doping with Nb2O5. The effects of doping have been described by M. Sacerdoti et al., J. Sold State Chem., 177, 1781-1788 (2004), J. Arbiol et al., J. Appl. Phys., 92(2), 853 (2002), B. M. Reddy et al., J. Mater. Sci. Lett., 17, 1913-1915 (1998), and H. Cui et al., J. Solid State Chem., 115, 187-191 (1995).
The formation on polymer substrates of oxide coatings using reactive magnetron sputtering and electron beam evaporation, respectively, has been described by Y. Shigesato (Proceed. 5th ICCG, Saarbrücken, 2004) and K. Lau et al. (Proceed. 5th ICCG, Saarbrücken, 2004). These methods require high expenditures and cost and the produced layers are of a thickness of only some 100 nanometers. TiO2 layers can also be produced by dip coating which has to be followed by a calcining step. Because of the thermal stress, this process and most thermal spraying methods are not suitable for the coating of polymers.
Furthermore, cold gas spraying (CGS) has been described as a method for coating a metal surface with another metal (see, e.g., J. Voyer et al., Development of Cold Gas Sprayed Coatings, S. 71-78, Thermal Spray 2003: Advancing the Science & Applying the Technology, C. Moreau and B. Marple (Eds.), ASM International Materials Park, Ohio (2003)). For building up a firmly adhering layer, the ductile behavior of the powder as well as of the surface to be coated play an important role. Metallic powders, such as Cu, Al, Ni, Ti and their alloys are blasted at a high speed of typically between 500 and 1,000 m/s and at temperatures of typically up to 300° C. onto a substrate and, as a result of plastic deformation, build up a firmly adhering layer there. The temperature of the process gas by means of which the particles area accelerated and heated typically amounts to from 300-600° C. It is therefore very clearly below the melting point of the powdery material as well as of the substrate. As disclosed by T. Stoltenhoff in Proc. ITSC, May 5-8, 2003, Orlando, Fla., during cold gas spraying of metal coatings, the metal powder particles undergo only slight changes in microstructure, crystal structure and oxidation state. An important process parameter is the speed of the particles before they impact on the substrate surface. In this case, each material has a critical speed above which the adhesion takes place. The impact speed of the particles is important for achieving a strong bond. Adhesion takes place when a material-specific critical speed is exceeded. This is determined by the characteristics of the material of the powder and the substrate and, in addition, depends on the temperature of the particles and of the substrate at the moment of the impact.
C. J. Li et al. (Proc. ITSC, May 10-12, 2004, Osaka, Japan) have disclosed the formation using powder spraying of thin, discontinuous TiO2 layers on a metal substrate. The thickness of the layer amounted to <15 μm. However, still no closed layer could be produced, so that its photocatalytic effect was limited because the UV energy was not optimally utilized. It has not been known from the literature that polymer surfaces can be coated with oxidic powders by means of cold-gas spraying.
Our own work has shown that photocatalytically very efficient layers can be applied to polymer surfaces by means of cold-gas spraying. The layers are characterized by a considerable layer thickness (>15 μm) which, on the one hand, protects the polymer substrate from degradation by UV radiation, which is not ensured in the case of other low-temperature coating processes, and, on the other hand, can optimally utilize the UV energy. The high photocatalytic activity is determined particularly by the high specific surface of the layer, that is its high roughness or porosity.
In contrast to a metal surface, the powder particles, when the polymer surface is bombarded, penetrate several μm deep into the polymer, and a firm bond is formed between the oxidic powder and the polymer. In the case of conventional coating techniques of polymer surfaces with oxidic layers, the considerable difference in the thermal coefficient of expansion leads to problems (forming of cracks, chipping, etc., as described by R. P. Shimshock in Proceed. 5th ICCG, Saarbrücken, 2004). Oxide/polymer bonds, which were produced by cold-gas spraying, surprisingly do not exhibit the expected temperature-related sensitivity.
For coating PET, PSU and PEEK surfaces with TiO2, the cold-gas spraying parameters listed in Table 1 were selected. PET is an abbreviation for polyethylene terephthalate, PSU is an abbreviation for polysulfone and PEEK is an abbreviation for polyetheerether ketone.
A schematic illustration of an exemplary system for cold gas spraying is shown in
Using the parameters of Table 1, homogeneous thin firmly adhering anatase layers were obtained whose structure was determined by micro-Raman spectroscopy. It is found that the layer consists entirely of the photocatalytically particularly active anatase modification of the titanium dioxide (
The layers were tested with respect to their photocatalytic efficiency in contact with a solution of 4-chlorophenol and sodium perchlorate under UV irradiation (λ>320 nm). A schematic of a Miniphoto reactor 300 for determining the photocatalytic activity of titanium dioxide layers is shown in
The coated test specimens 310 had the dimension of 12×8 mm. They were fixed in a standard cell for spectroscopy, which was filled with an aqueous solution of a 0.01 molar 4-chlorophenol and a 0.01 molar sodium perchlorate solution. The specimen fixed in the cell was irradiated by means of polychromatic UV light (wavelength>320 nm). In order to measure the photocatalytic activity, the pH change, which is proportional to the photocatalytic activity, was continuously measured by means of an electrode 320. A specimen of the same size, which was covered with a sedimented and calcined layer of TiO2 powder of Degussa Company, was used as the comparison specimen. A plot of the kinetic dependence of the pH value versus irradiation time via the photocatalytic reduction of 4-chlorophenol is shown in
All of the above-mentioned references are herein incorporated by reference in their entirety to the same extent as if each individual reference was specifically and individually indicated to be incorporated herein by reference in its entirety.
While the invention has been described with reference to preferred embodiments, it is to be understood that variations and modifications may be resorted to as will be apparent to those skilled in the art. Such variations and modifications are to be considered within the purview and scope of the invention as defined by the claims appended hereto.
