Title of Invention	A SUBSTRATE SUBSTANTIALLY TRANSPARENT WITH IMPROVED FUNCTIONALLY ADAPTABLE IN BUILDING, VEHICLES, URBAN FURNITURES AND DOMESTIC ELECTRICAL APPLIANCES.
Abstract	The invention relates to a substrate (1) substantially transparent with improved functionality adaptable in buildings, vehicles, urban furnitures, and domestic electrical appliances. It is provided on at least part of its surface with a first coating (2) comprising a layer or several stacked layers based on an at least partly oxidized derivative of silicon, selected from silicon dioxide, substoichiometric silicon oxides and a silicon oxycarbide, oxynitride or oxycarbonitride, said first coating (2) exhibiting hydrophilicity and being surmounted by a second coating (3) having photocatalytic properties, which comprises at least partly crystallized titanium oxide, said second coating (3) having a discontinuous or permeable structure.

Title of Invention

A SUBSTRATE SUBSTANTIALLY TRANSPARENT WITH IMPROVED FUNCTIONALLY ADAPTABLE IN BUILDING, VEHICLES, URBAN FURNITURES AND DOMESTIC ELECTRICAL APPLIANCES.

Abstract

The invention relates to a substrate (1) substantially transparent with improved functionality adaptable in buildings, vehicles, urban furnitures, and domestic electrical appliances. It is provided on at least part of its surface with a first coating (2) comprising a layer or several stacked layers based on an at least partly oxidized derivative of silicon, selected from silicon dioxide, substoichiometric silicon oxides and a silicon oxycarbide, oxynitride or oxycarbonitride, said first coating (2) exhibiting hydrophilicity and being surmounted by a second coating (3) having photocatalytic properties, which comprises at least partly crystallized titanium oxide, said second coating (3) having a discontinuous or permeable structure.

Full Text	SUBSTRATE WITH A SELF-CLEANING COATING The invention relates to various types of material that may be found in buildings, vehicles, urban furniture or in domestic electrical appliances, namely in particular: transparent substrates, made of glass or polymer, intended to serve as glazing, for example as a display screen; ceramic or glass-ceramic substrates that can be used for example in domestic electrical appliances; architectural materials, such as roof tiles, floor tiles, stone, cementitious compositions and metal surfaces; and fibrous mineral materials, such as glass insulation wool or textile glass yarns, that can be used as filtration material, for making false ceilings, etc. Recent studies have been carried out for the purpose of trying to improve the comfort of these materials when in use, especially to make them easier to clean, and two broad approaches have been studied in order to give these materials such a functionality. According to a first approach, functional coatings having the feature of being highly hydrophilic have been studied and developed. This is especially the case for coatings based on silicon oxide or oxycarbide that can be deposited on glazing according to the teaching of patent WO 01/32578. This type of coating has a pronounced antisoiling effect with respect to dust, most particularly with respect to mineral dust: simply running water over the surface of such a coating, which is highly "wetting", allows the dust to be carried away. Such running water may be natural (rain) if the substrate is used outdoors and exposed appropriately. It may also be induced: this becomes a washing operation, but one that is very easy since there is no need to rub the substrate nor is there any need to use detergents. The substrates thus treated become soiled to a lesser extent and less quickly. It is thus possible to space out more conventional washing operations with detergents (especially as regards windows). However, this hydrophilic coating has a less pronounced effect with regard to organic dust (for example that from motor vehicle exhaust gas residues, various hydrocarbon residues in the vicinity of airports, or more simply fingerprints). Such organic soiling tends to accumulate on the surface of the coating, progressively reducing, at least locally, its hydrophilicity. Its fouling delay function is therefore real, but could be improved depending on the type of soiling encountered and on the type of pollution to which the substrate is exposed. According to a second approach, functional coatings having photocatalytic properties have been developed. These are especially coatings comprising TiO2 at least partially crystallized especially in the anatase form, which have for example been described in patents WO 97/10185, WO 97/10186, WO 99/44954 and WO 01/66271. This type of semiconducting material, based on an optionally doped metal oxide (there are also other oxides that can be photocatalytic, such as ZnO, etc), is capable through the effect of radiation of suitable wavelength, of initiating radical reactions that cause organic compounds to oxidize: this type of coating, when sufficiently exposed to ad hoc radiation (generally ultraviolet, and possibly visible range), is therefore very effective for degrading organic soiling. Furthermore, it has been discovered that, especially when the coatings are based on titanium oxide, they also exhibit a certain hydrophilicity when exposed for a sufficiently long time to said radiation. This coating is therefore very effective in that it can degrade organic soiling and, through its hydrophilicity, remove mineral soiling. However, its activity is dependent on its exposure (for a long enough time) to radiation (of sufficient intensity) of ad hoc wavelength. The behavior of this type of coating therefore depends strongly on the environmental conditions in the case of outdoor exposure, especially the sunshine and rain conditions. Likewise, in the absence of suitable illumination, its activity at night tends to be less than its activity during the day. The object of the invention is therefore to further improve the functionality imparted by these various types of "self-cleaning" or "fouling delay" coatings. The invention is aimed in particular at obtaining coatings that can be of enhanced efficiency and can be more "multipurpose" with regard to various aspects: firstly with regard to soiling of different chemical nature and then with regard to varied environmental conditions when the substrate is used outdoors. The object of the invention is more particularly to obtain coatings that can, even under mediocre irradiation conditions, and even at night, exhibit a certain antisoiling activity. The subject of the invention is firstly a substrate that may essentially be transparent, especially one based on glass or one or more polymers, or may be made of a ceramic or glass-ceramic, or may even be an architectural material (of the type comprising a wall render, a concrete slab or block, architectural concrete, roof tile, material of cementitious composition, terracotta, slate, stone, or may even be a fibrous substrate, based on glass of the mineral insulation wool type, or glass reinforcement yarns). This substrate is characterized in that it is provided on at least part of its surface with a first coating comprising a layer or several stacked layers preferably based on an at least partly oxidized derivative of silicon, chosen from silicon dioxide, substoichiometric silicon oxides and silicon oxycarbide, silicon oxynitride or silicon oxycarbonitride. This first coating is chosen so as to exhibit hydrophilicity and is surmounted by a second coating chosen so as to exhibit photocatalytic properties. This second coating preferably comprises at least partly crystallized titanium oxide, especially in anatase form. This second coating has a discontinuous/permeable structure. These terms are understood to mean that the second coating is sufficiently porous and sufficiently "noncovering" to allow access to a certain portion of the external surface of the subjacent first coating. It is advantageous to choose a distribution of the second (photocatalytic) coating on the first (hydrophilic) coating that is "regular", or as regular as possible, on the scale of 1 mm2 or 1 cm2 of substrate, and to have approximately the same amount and/or the same thickness of the second coating, which is preferably distributed approximately in the same way on this scale. Further details will be given later as regards the way in which the second coating is distributed on the first and how the structure of the second coating thus permits the subjacent coating to come into contact with the external atmosphere, but two cumulative or alternative situations are especially possible, namely the second coating may be chosen to have a thinness such that it is in fact in the form of islands distributed more or less randomly on the surface of the subjacent first coating. It may also have a porous structure, and an at least partly open porosity, that lets the water from the ambient atmosphere reach the first coating. Preferably, as regards the first coating and the second, the thicknesses remain within the interferential thickness range, for example of the order of at most one hundred nanometers in the case of the first coating. Especially in the case of coatings suitable for transparent substrates of the glazing type, these very small thicknesses guarantee that, even if the second coating is in fact only a collection of more or less separate islands, there is no inhomogeneity in the optical properties associated with the discontinuity of the second coating, especially no iridescence. It has therefore been discovered in the invention that there is a very considerable synergy between the two coatings with complementary properties: the hydrophilic first coating is effective more for mineral-type soiling, whatever the irradiation conditions. It can be active through the effect of rain or by water spray. The second coating is effective for organic soiling and even mineral soiling when it has a degree of hydrophilicity, its effectiveness being dependent on the conditions of exposure to the appropriate radiation (for most of the time ultraviolet and/or visible radiation). It is furthermore designed to leave (at least partly) the first, subjacent coating its antisoiling property, allowing water to pass through it (and the dust to be carried away therewith). Furthermore, the at least partly preserved hydrophilicity of the first coating retains its antifogging and anticondensation effects, which are also highly appreciated. This double coating is straightaway very multipurpose: in the presence of irradiation, the effectiveness in delaying fouling is very high, making use of the complementary properties of the two coatings. Even in the case of low irradiation (or at night), a certain effectiveness is retained, at least as regards mineral soiling, either thanks to natural rain or more simply by water spray. The subjacent (hydrophilic) first coating thus makes it possible to readily remove mineral soiling which is undesirable, as it is unattractive and also because its accumulation could end up deactivating/passivating the photocatalytic properties of the photocatalytic second coating. It is therefore truly a combination of effects that gives excellent results, whereas it might be expected that the photocatalytic second coating, owing to its discontinuous/porous character, would add nothing or almost nothing in terms of antisoiling properties to the subjacent hydrophilic coating, or, worse still, would remove the subjacent hydrophilic coating of its antisoiling, antifogging and anticondensation properties. Advantageously, the substrate according to the invention is essentially transparent, flat or curved, of the glazing type, impressed or not, as it is in this type of application that the accumulation of soiling that prevents visibility is the most irksome and that washing operations are really necessary in order to guarantee their transparency. Preferably, the first coating of hydrophilic character may be of the type described in the aforementioned patent WO 01/32578. Advantageously, it has a refractive index of between 1.45 and 1.80, especially between 1.50 and 1.75, for example between 1.55 and 1.68. Such a relatively low index, on a transparent substrate of the glass type, makes it possible to prevent a reflecting effect that may be deemed unattractive. This coating therefore advantageously comprises Si, 0, and possibly carbon and nitrogen. However, it may also include materials in a minor proportion compared with silicon, for example metals such as Al, Zn or Zr. This coating may be deposited by sol-gel or by pyrolysis, especially by CVD (chemical vapor deposition). The latter technique can be used to obtain SiOxCy or SiO2 coatings quite easily, especially by deposition directly on the ribbon of float glass in the case of glass substrates. However, it is also possible to deposit such a coating by a vacuum technique, for example sputtering using an Si (optionally doped) target or a silicon suboxide target (for example in an oxidizing and/or nitriding reactive atmosphere). This first coating preferably has a thickness of at least 5 nm, especially a thickness between 10 and200 nm, for example between30 and120 nm. To enhance its hydrophilicity, it has been shown that it is advantageous for this coating to have a certain roughness. This may especially take the form of nanoscale protuberances and/or indentations. They may more particularly be protuberances, at least some of which are not touching: it is thus possible to have a coating whose external face has a relatively smooth profile from which emerge protuberances that may be overlapping or touching, but at least some of which are discrete. Such surface structuring is achieved most particularly with coatings obtained by pyrolysis. In general it is also possible using this type of technique to obtain quite dense coatings that adhere strongly to the carrier substrate, and are therefore durable, to the benefit of the invention of course. These protuberances/indentations vary in size, for example with a diameter distribution between 5 and 300 nm, especially 50 and 100 nm. The term "diameter" is understood here in the broad sense, by likening these protuberances/indentations to solid hemispheres (protuberances) or hemispherical voids (indentations). It goes without saying that this is an average size and that protuberances/indentations of more random shape, for example more elongated, are included. These protuberances and/or indentations may also have a height (in the case of protuberances) or a depth (in the case of indentations) of between 5 and 100 nm, especially between 10 and 50 nm. This gives an indication of the maximum value for each protuberance/indentation whose size it is desired to determine. One way of measuring these dimensions consists in carrying out measurements based on photographs taken by scanning electron microscopy (SEM). Such photographs can also be used to determine the distribution of these indentations/protuberances per unit area of the substrate. It is thus possible to have a number of protuberances/indentations for this first coating of between5 and300 per µm2, especially between20 and 200 per µm2, of coated substrate. One way of measuring these hydrophilicity-enhancing protuberances/indentations consists in measuring the rms roughness expressed in nm. This first coating may thus have an rms roughness of between 4 and 12 nm, especially between 5 and 10 nm, and more particularly between 6 and 9 nm. The second coating, that exhibiting photocatalytic properties, is preferably thin, that is to say it has a thickness of at most 10 nm, especially a thickness of at most 8 or 5 or 3 nm, in the regions where it actually overlaps the first coating. In fact, it may be so thin as to tend toward the detection limits of the machines normally used to evaluate interferential layer thicknesses. As mentioned above, the term "coating" is to be taken in its broadest sense insofar as this coating may be discontinuous, in the form of at least partly discrete islands, or so porous as to be considered as discontinuous. It is in fact just this point that is surprising in the invention, that such a coating, despite its very "tenuous" character, does provide a certain functionality. Its presence may, perhaps more justifiably, be quantified not so much by a thickness value but by the amount of material deposited per unit area of substrate (any discontinuity in the coating is thus taken into account). In the case here, this amount may advantageously be at most 10 micrograms per cm2, especially at most 5 or 3 micrograms per cm2. It is preferable for this to be within the range from about 0.5 to 3 micrograms per cm2, i.e. really very small amounts (compared with the amount of material per cm2 provided, for example, by an SiOC-based hydrophilic first coating with a thickness of around fifty nanometers, which is already about 10 micrograms per cm2 of substrate for an SiOC material, albeit less dense than bulk TiO2). Advantageously, this second coating will therefore be able to let the first coating "breathe" and allow at least part of the antisoiling activity associated with its hydrophilicity, that it would have in its absence, to be retained. The second coating is preferably deposited by sol-gel, or by CVD-type pyrolysis or by a vacuum technique of the sputtering type. From an industrial standpoint, it is most beneficial to produce this double coating continuously, by depositing the first coating and then the second by chemical vapor deposition on a ribbon of float glass, for example, when glass substrates are involved. Advantageously, the second coating is essentially based on optionally doped titanium oxide, consisting of grains or crystallites with a diameter of between 0.5 and 100 nm, especially between 2 and20 nm. Here again the term "diameter" is to be taken in the broad sense - it is more a determination of the size of the crystallites. The shape of the grains may approach that of a sphere or have an elongate shape of the rice grain type, or have a completely random shape. These grains/crystallites may be at least partly touching. They may also exhibit some cohesion owing to amorphous oxide that will incorporate/bind these crystallized grains. Preferably, the ratio of the diameter of the protuberances on the external surface of the first (hydrophilic) coating to that of the grains or crystallites of the second (photocatalytic) coating is at least 2, especially at least 4, 5 or even at least 10. Advantageously, the second coating will "follow" the roughness of the first, if there is any roughness, and even sometimes enhance it. Thus, the rms surface roughness in nm of the substrate coated with the hydrophilic first coating and with the photocatalytic second coating will be between 4 and 15 nm, especially between 5 and 12 nm, more particularly between 7 and 10 nm. Taking an embodiment described above in which the external surface of the first coating is provided with indentations/protuberances and in which the second coating comprises grains/crystallites, these grains/crystallites may be placed between these indentations/protuberances and optionally cover, at least partly, these indentations/protuberances. Advantageously, the transparent, especially glass, substrate of the glazing type, which is provided with the double coating according to the invention, has a light reflection RL on the coating(s) side of at most 12%, especially at most11%, under illuminant D65. This thus amounts to a coating of very low reflectivity that therefore does not penalize the substrate optically, which remains quite "neutral" optically. Its colorimetric response in reflection may be very slight, and in neutral colors fairly perceptible (or almost imperceptible) to the eye, and preferably in the green-blues. This colorimetric response may for example be quantified by a* and b* values in the (L,a,b) colorimetry system, in which preferably b* is of negative sign. Preferably b* and a* are negative. In absolute values, a* and b* are preferably less than 5 or 4 or 3. Advantageously, the combination of the first and second coatings has a photocatalytic activity characterized by a rate of degradation of palmitic acid of at least 5 nm/h, especially at least 10 nm/h when exposed to appropriate radiation, especially ultraviolet radiation. The conditions for the test measuring this rate of degradation will be explained in detail during the subsequent description of the examples. Also advantageously, the combination of the two coatings exhibits hydrophilicity characterized by a water contact angle of at most 10° or 5°, with or without exposure to radiation in the ultraviolet or the visible. The subject of the invention is also the application of the substrates according to the invention, especially those that are essentially transparent, to the manufacture of "self-cleaning" glazing that can provide, simultaneously, antisoiling, antifogging and anticondensation behavior. This may be glazing for buildings of the double-glazing type, vehicle windows of the windshield, rear window, sunroof, side window or rear-window type. They may also be windows for trains, aircraft and ships. It may also be utilitarian glazing, such as aquarium glass, shop window glass or greenhouse glass, or else glazing used in interior furnishings or in urban furniture. It may also be glazing used as display screens of the television, computer or telephone screen type. This type of coating may also be applied to electrically controllable glazing, such as wire-type or layer-type heated windows, electrochromic glazing, glazing incorporating a liquid-crystal film, electroluminescent glazing or photovoltaic glazing. The substrate according to the invention, apart from its application as glazing, may be made of any architectural material that can be used for manufacturing partitions, wall claddings, roofing, flooring, either indoors or outdoors (metal, wood, stone, cement, concrete, terracotta, ceramic, wall render, etc.). The substrate, if instead based on a mineral fibrous material (glass, rock, silica, etc.), may serve as filtration material or else may be used for false ceilings, which are not easy to clean. The invention will be described below with the aid of nonlimiting examples and figures 1 to 3. All the figures are SEM micrographs of the examples. In all the examples, the substrate 1 is a silica-soda-lime clear glass 4 mm in thickness (of the type of glass sold by Saint-Gobain Glass France under the name SGG Planilux). Example 1 This example relates to the deposition, on the glass 1 again in the form of a ribbon of float glass, of a first coating 2 based on silicon oxycarbide, denoted for convenience by SiOC (without prejudging the actual amount of oxygen and carbon in the coating). This coating 2 was deposited by CVD using Si precursors, in particular using an SiH4/ethylene mixture diluted in nitrogen, with the aid of a nozzle placed above and transversely to the ribbon float glass 1 of a flat glass production line, in the float chamber, when the glass was still at a temperature of about 600 to 700°C. The coating obtained had a thickness of about 50 nm and a refractive index of about 1.55. Still on the float line in the float chamber, and at the same glass temperature, the titanium-oxide-based coating 3 was deposited, by means of a second nozzle, using titanium isopropylate diluted in nitrogen. This coating was very thin, probably "noncovering" with respect to the subjacent coating. Its thickness was determined to be less than 5 nm, corresponding to an amount of TiO2 of the order of 1 microgram per cm of substrate. The photographs shown in figures 1a, 1b and 1c relate to this example 1, once the glass ribbon had been cut from the float line: they show, on two different scales, seen from above and, in the case of figure 1c, obliquely, the coating 2 that was seeded with pseudo-circular protuberances 4 in the plane of section, and having a diameter of about 30 to 70 nm. They also show traces of the coating 3, in the form of grains 5 much smaller in size than the protuberances 4. These grains lie between the protuberances 4 and perhaps also at least on these protuberances, but this is difficult to confirm just from these micrographs. These grains have a size of around 2 to 10 nm. The glass 1 was then subjected to two series of tests, one a natural aging test and the other an accelerated aging test. - Natural aging: The glass 1 provided with a double coating was exposed on the outside for 6 months at the Charles de Gaulle airport near Paris, so as to be inclined and in direct contact with rain and sunshine. This is because the environment of an airport is a very good test environment as it is a highly polluted atmosphere, especially polluted with higher hydrocarbon contents in the air than elsewhere. After 6 months, it was found that the glass retained a clean and wetting appearance: the glass treated according to the invention therefore has actual "self-cleaning" properties, even under environmental conditions that are neither very sunny nor very rainy, as encountered in the Paris region. It is therefore capable of ridding itself of organic soiling, even with a very thin if not discontinuous photocatalytic coating 3. In addition, it remains hydrophilic. For comparison, the uncoated glass of untreated SGG Planilux type, subjected to exactly the same environmental conditions, loses its wetting character after 15 days of exposure, with visible traces of droplets and dust. - Accelerated aging: The photocatalytic activity of the treated glass according to example 1 was firstly measured by what is called the palmitic acid test. This test consists in depositing, on 15 cm2 of the surface of the treated glass, by spraying, a palmitic acid solution (8 grams of acid per 1 l of chloroform) with a glass/spray distance of 20 cm, on a vertical substrate in 3 to 4 successive passes. Next, the glass is weighed in order to determine the thickness in nanometers of palmitic acid deposited (by weighing the glass specimen before deposition of the palmitic acid). The glass was then exposed to UVA with an intensity of about 30 W/m2. The photocatalytic activity was then calculated as the rate of disappearance v (in nm/h) of palmitic acid, this rate being defined as follows: v(nm/h) = palmitic acid thickness (nm) / (2 x t ½ disappearance (h)). The value v for the treated surface of the treated glass was initially about 10 nm/h. Its water contact angle was 5 - this surface was therefore strongly hydrophilic and also photocatalytic. • Variable environment test This test was carried out according to the NF P 78 451 standard. It involves subjecting the glass to 4 cycles per 24 hours, with hold periods of 2 hours at 55°C and 95% relative humidity, then 1 hour at -15°C, with transitions lasting 1 hour 30 minutes. The water contact angle was measured every 10 days as follows: the glass was exposed for 20 minutes to UV and then stored in the dark for 72 hours. The measurement was then carried out, this being an average of three measurements on three different drops. After 10 days of testing, the water contact angle, which was 5° initially, increased to 10°. Then, after 20 days, the water contact angle dropped to 5°. This 5° value then remained approximately constant for up to 55 days. These measurements therefore merely prove that the hydrophilicity of the treated glass is indeed preserved over time, this hydrophilicity probably being a combination of the hydrophilicity of the first and of the second coating. • High humidity test This test was carried out according to the EN 1096-2 standard. It involves subjecting the glass to a temperature of 40°C in a chamber saturated with moisture, with a relative humidity of greater than 95%, with water having a conductivity of less than 30 µS and a pH of greater than 5 running over the treated face of the glass. The treated glass having undergone this test was then exposed for 10 and 20 days to UV and then stored for 72 hours in the dark, as in the previous test. The water contact angle measurement was also an average of three measurements. After 10 days, the water contact angle was 10° and after 20 days it had dropped back down to 5°. • Neutral salt fog test This test was carried out according to the EN 1036 standard. It involves placing the glass in a chamber at 35°C with a fine spray of hot (35°C) neutral (5% NaCl in water) brine, the treated surface being exposed to this fog. The water contact angle of the treated surface was again measured under the same conditions as the previous two tests. The contact angle remained at 5° for 55 days. Example 2 This example is similar to example 1, but the coating 3 was "thicker", by sputtering a larger amount of titanium oxide precursor: in the case of example 2, the amount of TiO2 deposited on the coating 2 was about 2.3 micrograms per cm2 of substrate. The SEM photographs of figures 2a, 2b and 2c show the treated surface seen from above and obliquely, on two different scales: they show a structure similar to that of example 1. The initial photocatalytic activity of the treated surface was 20 nm/h and its initial water contact angle was 5°. After 15 days of the variable environmental test, the water contact angle was 10°. It was even 18° after 15 days of high-humidity testing (same conditions as in example 1). Everything occurs as if the presence in larger quantity of the photocatalytic TiO2 increases the photocatalytic activity of the coating by a factor of 2, but there should be a reason (not yet explained) why the hydrophilicity decreases slightly after accelerated environmental aging. However, it should be noted that a hydrophilic coating is still present, within the meaning of the term "hydrophilic", with a water contact angle of at most 20° after having undergone the tests. For comparison, figure 3 shows an SEM photograph seen from above of a glass coated only with the SiOC coating 2: the protuberances may again be seen, but the TiO2 grains lying between these protuberances are no longer present. WE CLAIM 1. A substrate (1) substantially transparent with improved functionality adaptable in buildings, vehicles, urban furnitures, and domestic electrical appliances, characterized in that it is provided on at least part of its surface with a first coating (2) comprising a layer or several stacked layers based on an at least partly oxidized derivative of silicon, selected from silicon dioxide, substoichiometric silicon oxides and a silicon oxycarbide, oxynitride or oxycarbonitride, said first coating (2) exhibiting hydrophilicity and being surmounted by a second coating (3) having photocatalytic properties, which comprises at least partly crystallized titanium oxide, said second coating (3) having a discontinuous or permeable structure. 2. The substrate as claimed in claim 1, comprising glass or polymer, intended to serve as glazing, for example, a display screen. 3. The substrate as claimed in claim 1, comprising ceramic or glass-ceramic adaptable in domestic electrical appliances. 4. The substrate as claimed in claim 1, comprising architectural material for example, roof tile, architectural concrete, a wall render, concrete slab cr block, material of cementitious composition, terracotta, slate, stone, or metal surface. 5. The substrate as claimed in claim 1, comprising fibrous mineral materials for example, glass-insulation wool or textile glass yarns. 6. The substrate as claimed in claim 1, wherein said substrate is substantially transparent, flat or curved, of the impressed glazing type. 7. The substrate (1) as claimed in one of the preceding claims, wherein the refractive index of the first coating (2) is between 1.45 and 1.80, preferably 1.50 and 1.75, more preferably 1.55 to 1.68. 8. The substrate (1) as claimed in one of the preceding claims, wherein the first coating (2) is deposited by sol-gel or by pyrolysis, in particular chemical vapor deposition (CVD) or by a vacuum technique of the sputtering type. 9. The substrate (1) as claimed in one of the preceding claims, wherein the first coating (2) has a minimum thickness of 5 nm, preferably between 10 and 200 nm, and more preferably between 30 and 120 nm. 10.The substrate (1) as claimed in one of the preceding claims, wherein the first coating (2) is rough and has an external surface with one cf nanoscale protuberances and indentations, or a combination of both. 11.The substrate (1) as claimed in claim 6, wherein the first coating (2) has an external surface exhibiting protuberances some of the protuberances are not touching each other. 12.The substrate (1) as claimed in claim 10, or claim 11, wherein the first coating (2) has, on the external surface, one of protuberances and indentations, or a combination of both with a diameter of between 5 and 300 nm, preferably between 50 and 100 nm. 13.The substrate (1) as claimed in claims 10 to 11, wherein the first coating (2) has on the external surface, one of protuberances and indentations or a combination of both with one of a height and a depth of between 5 and 100 nm, preferably between 10 and 50 nm. 14.The substrate (1) as claimed in claims 10 to 13, wherein the first coating (2) has an external surface comprising between 5 and 300 protuberances, preferably between 20 and 200 protuberances per µm2 of the substrate. 15.The substrate (1) as claimed in claims 10 to 14, wherein the first coating (2) has an rms roughness of between 4 and 12 nm, preferably between 5 and 10 nm and more preferably between 6 and 9 nm. 16.The substrate (1) as claimed in one of the preceding claims, wherein the second coating (3) has a maximum thickness of 10 nm, preferably 8 or 5 or 3 nm, in the regions of overlap with the first coating (2). 17.The substrate (1) as claimed in one of the preceding claims, wherein the second coating (3) is based on optionally doped titanium oxide comprising grains or crystallites with a diameter of between 0.5 and 100 nm, preferably between 2 and 20 nm. 18.The substrate (1) as claimed in claim 10 and claim 17, wherein the second coating (3) is based on optionally doped titanium oxide comprising grains or crystallites, the minimum diameter of the first coating (2) to the diameter of the grains or crystallites of the second coating (3) is 2, particularly 4, 5 or 10. 19.The substrate (1) as claimed in one of the preceding claims, wherein the substrate provided with the first (2) and second (3) coatings has an rms roughness of between 4 and 15 nm, preferably between 5 and 12 nm and more preferably between 7 and 10 nm. 20.The substrate (1) as claimed in one of the receding claims, wherein the second coating (3) follows the roughness of the first coating (2). 21.The substrate as claimed in claim 11 and 17, wherein the grains/crystallites of the second coating (3) lie between one of the indentations and protuberances or a combination of both of the external surface of the first coating (2) and partially cover, said one of the indentations and protuberances, or a combination of both. 22.The substrate (1) as claimed in one of the preceding claims, wherein the second coating (3) corresponds to a maximum amount of material of 10 micrograms per cm2 of substrate, preferably 5 or 3 micrograms per cm2 of the substrate, more preferably about 0.5 to 3 micrograms per cm2. 23.The substrate (1) as claimed in cone of preceding claims, wherein the second coating (3) is deposited by sol-gel, by pyrolysis, preferably chemical vapor deposition or by a vacuum technique of the sputtering type. 24.The glass substrate (1) as claimed in one of the preceding claims, wherein the first and second coatings are deposited by chemical vapor deposition on a ribbon of float glass. 25.The substrate (1) as claimed in one of the preceding claims, comprising, when provided with the first and second coatings, a maximum light reflection on the coating side Ri of 12%, preferably 11%, more preferably combined with a* and b* values such that 2 26.The substrate (1) as claimed in one of the preceding claims, wherein the combination of the first and second coatings (2, 3) exhibits photocatalytic activity characterized by a minimum rate of palmitic acid degradation of 5 nm/h, preferably 10 nm/h. 27.The substrate (1) as claimed in one of the preceding claims, wherein the combination of the first and second coatings (2, 3) exhibits hydrophilicity characterized by a water maximum contact angle of 20°, preferably 10°, or 5° with or without exposure to radiation in the ultraviolet and/or in the ordinarily visible context. 28. A "self-cleaning", particularly antifogging, anticondensation and antisoiling, glazing, comprising a substrate as claimed in any of the preceding claims. The invention relates to a substrate (1) substantially transparent with improved functionality adaptable in buildings, vehicles, urban furnitures, and domestic electrical appliances. It is provided on at least part of its surface with a first coating (2) comprising a layer or several stacked layers based on an at least partly oxidized derivative of silicon, selected from silicon dioxide, substoichiometric silicon oxides and a silicon oxycarbide, oxynitride or oxycarbonitride, said first coating (2) exhibiting hydrophilicity and being surmounted by a second coating (3) having photocatalytic properties, which comprises at least partly crystallized titanium oxide, said second coating (3) having a discontinuous or permeable structure.

Full Text

SUBSTRATE WITH A SELF-CLEANING COATING
The invention relates to various types of material that may be found in
buildings, vehicles, urban furniture or in domestic electrical appliances, namely
in particular:
transparent substrates, made of glass or polymer, intended to serve as
glazing, for example as a display screen;
ceramic or glass-ceramic substrates that can be used for example in
domestic electrical appliances;
architectural materials, such as roof tiles, floor tiles, stone, cementitious
compositions and metal surfaces; and
fibrous mineral materials, such as glass insulation wool or textile glass
yarns, that can be used as filtration material, for making false ceilings, etc.
Recent studies have been carried out for the purpose of trying to improve
the comfort of these materials when in use, especially to make them easier to
clean, and two broad approaches have been studied in order to give these
materials such a functionality.
According to a first approach, functional coatings having the feature of
being highly hydrophilic have been studied and developed. This is especially the
case for coatings based on silicon oxide or oxycarbide that can be deposited on
glazing according to the teaching of patent WO 01/32578. This type of coating
has a pronounced antisoiling effect with respect to dust, most particularly with
respect to mineral dust: simply running water over the surface of such a coating,
which is highly "wetting", allows the dust to be carried away. Such running
water may be natural (rain) if the substrate is used outdoors and exposed
appropriately. It may also be induced: this becomes a washing operation, but
one that is very easy since there is no need to rub the substrate nor is there any
need to use detergents. The substrates thus treated become soiled to a lesser
extent and less quickly. It is thus possible to space out more conventional
washing operations with detergents (especially as regards windows). However,
this hydrophilic coating has a less pronounced effect with regard to organic dust
(for example that from motor vehicle exhaust gas residues, various hydrocarbon
residues in the vicinity of airports, or more simply fingerprints). Such organic
soiling tends to accumulate on the surface of the coating, progressively
reducing, at least locally, its hydrophilicity. Its fouling delay function is
therefore real, but could be improved depending on the type of soiling
encountered and on the type of pollution to which the substrate is exposed.
According to a second approach, functional coatings having
photocatalytic properties have been developed. These are especially coatings
comprising TiO2 at least partially crystallized especially in the anatase form,
which have for example been described in patents WO 97/10185, WO 97/10186,
WO 99/44954 and WO 01/66271. This type of semiconducting material, based on
an optionally doped metal oxide (there are also other oxides that can be
photocatalytic, such as ZnO, etc), is capable through the effect of radiation of
suitable wavelength, of initiating radical reactions that cause organic compounds
to oxidize: this type of coating, when sufficiently exposed to ad hoc radiation
(generally ultraviolet, and possibly visible range), is therefore very effective for
degrading organic soiling. Furthermore, it has been discovered that, especially
when the coatings are based on titanium oxide, they also exhibit a certain
hydrophilicity when exposed for a sufficiently long time to said radiation. This
coating is therefore very effective in that it can degrade organic soiling and,
through its hydrophilicity, remove mineral soiling. However, its activity is
dependent on its exposure (for a long enough time) to radiation (of sufficient
intensity) of ad hoc wavelength. The behavior of this type of coating therefore
depends strongly on the environmental conditions in the case of outdoor
exposure, especially the sunshine and rain conditions. Likewise, in the absence
of suitable illumination, its activity at night tends to be less than its activity
during the day.
The object of the invention is therefore to further improve the
functionality imparted by these various types of "self-cleaning" or "fouling
delay" coatings. The invention is aimed in particular at obtaining coatings that
can be of enhanced efficiency and can be more "multipurpose" with regard to
various aspects: firstly with regard to soiling of different chemical nature and
then with regard to varied environmental conditions when the substrate is used
outdoors. The object of the invention is more particularly to obtain coatings that
can, even under mediocre irradiation conditions, and even at night, exhibit a
certain antisoiling activity.
The subject of the invention is firstly a substrate that may essentially be
transparent, especially one based on glass or one or more polymers, or may be
made of a ceramic or glass-ceramic, or may even be an architectural material
(of the type comprising a wall render, a concrete slab or block, architectural
concrete, roof tile, material of cementitious composition, terracotta, slate,
stone, or may even be a fibrous substrate, based on glass of the mineral
insulation wool type, or glass reinforcement yarns). This substrate is
characterized in that it is provided on at least part of its surface with a first
coating comprising a layer or several stacked layers preferably based on an at
least partly oxidized derivative of silicon, chosen from silicon dioxide,
substoichiometric silicon oxides and silicon oxycarbide, silicon oxynitride or
silicon oxycarbonitride. This first coating is chosen so as to exhibit hydrophilicity
and is surmounted by a second coating chosen so as to exhibit photocatalytic
properties. This second coating preferably comprises at least partly crystallized
titanium oxide, especially in anatase form. This second coating has a
discontinuous/permeable structure. These terms are understood to mean that
the second coating is sufficiently porous and sufficiently "noncovering" to allow
access to a certain portion of the external surface of the subjacent first coating.
It is advantageous to choose a distribution of the second (photocatalytic) coating
on the first (hydrophilic) coating that is "regular", or as regular as possible, on
the scale of 1 mm2 or 1 cm2 of substrate, and to have approximately the same
amount and/or the same thickness of the second coating, which is preferably
distributed approximately in the same way on this scale. Further details will be
given later as regards the way in which the second coating is distributed on the
first and how the structure of the second coating thus permits the subjacent
coating to come into contact with the external atmosphere, but two cumulative
or alternative situations are especially possible, namely the second coating may
be chosen to have a thinness such that it is in fact in the form of islands
distributed more or less randomly on the surface of the subjacent first coating.
It may also have a porous structure, and an at least partly open porosity, that
lets the water from the ambient atmosphere reach the first coating. Preferably,
as regards the first coating and the second, the thicknesses remain within the
interferential thickness range, for example of the order of at most one hundred
nanometers in the case of the first coating. Especially in the case of coatings
suitable for transparent substrates of the glazing type, these very small
thicknesses guarantee that, even if the second coating is in fact only a collection
of more or less separate islands, there is no inhomogeneity in the optical
properties associated with the discontinuity of the second coating, especially no
iridescence.
It has therefore been discovered in the invention that there is a very
considerable synergy between the two coatings with complementary properties:
the hydrophilic first coating is effective more for mineral-type soiling, whatever
the irradiation conditions. It can be active through the effect of rain or by water
spray. The second coating is effective for organic soiling and even mineral soiling
when it has a degree of hydrophilicity, its effectiveness being dependent on the
conditions of exposure to the appropriate radiation (for most of the time
ultraviolet and/or visible radiation). It is furthermore designed to leave (at least
partly) the first, subjacent coating its antisoiling property, allowing water to
pass through it (and the dust to be carried away therewith). Furthermore, the at
least partly preserved hydrophilicity of the first coating retains its antifogging
and anticondensation effects, which are also highly appreciated.
This double coating is straightaway very multipurpose: in the presence of
irradiation, the effectiveness in delaying fouling is very high, making use of the
complementary properties of the two coatings. Even in the case of low
irradiation (or at night), a certain effectiveness is retained, at least as regards
mineral soiling, either thanks to natural rain or more simply by water spray. The
subjacent (hydrophilic) first coating thus makes it possible to readily remove
mineral soiling which is undesirable, as it is unattractive and also because its
accumulation could end up deactivating/passivating the photocatalytic
properties of the photocatalytic second coating. It is therefore truly a
combination of effects that gives excellent results, whereas it might be
expected that the photocatalytic second coating, owing to its
discontinuous/porous character, would add nothing or almost nothing in terms of
antisoiling properties to the subjacent hydrophilic coating, or, worse still, would
remove the subjacent hydrophilic coating of its antisoiling, antifogging and
anticondensation properties.
Advantageously, the substrate according to the invention is essentially
transparent, flat or curved, of the glazing type, impressed or not, as it is in this
type of application that the accumulation of soiling that prevents visibility is the
most irksome and that washing operations are really necessary in order to
guarantee their transparency.
Preferably, the first coating of hydrophilic character may be of the type
described in the aforementioned patent WO 01/32578. Advantageously, it has a
refractive index of between 1.45 and 1.80, especially between 1.50 and 1.75,
for example between 1.55 and 1.68. Such a relatively low index, on a
transparent substrate of the glass type, makes it possible to prevent a reflecting
effect that may be deemed unattractive.
This coating therefore advantageously comprises Si, 0, and possibly
carbon and nitrogen. However, it may also include materials in a minor
proportion compared with silicon, for example metals such as Al, Zn or Zr. This
coating may be deposited by sol-gel or by pyrolysis, especially by CVD (chemical
vapor deposition). The latter technique can be used to obtain SiOxCy or SiO2
coatings quite easily, especially by deposition directly on the ribbon of float
glass in the case of glass substrates. However, it is also possible to deposit such
a coating by a vacuum technique, for example sputtering using an Si (optionally
doped) target or a silicon suboxide target (for example in an oxidizing and/or
nitriding reactive atmosphere).
This first coating preferably has a thickness of at least 5 nm, especially a
thickness between 10 and200 nm, for example between30 and120 nm.
To enhance its hydrophilicity, it has been shown that it is advantageous
for this coating to have a certain roughness. This may especially take the form of
nanoscale protuberances and/or indentations. They may more particularly be
protuberances, at least some of which are not touching: it is thus possible to
have a coating whose external face has a relatively smooth profile from which
emerge protuberances that may be overlapping or touching, but at least some of
which are discrete. Such surface structuring is achieved most particularly with
coatings obtained by pyrolysis. In general it is also possible using this type of
technique to obtain quite dense coatings that adhere strongly to the carrier
substrate, and are therefore durable, to the benefit of the invention of course.
These protuberances/indentations vary in size, for example with a
diameter distribution between 5 and 300 nm, especially 50 and 100 nm. The
term "diameter" is understood here in the broad sense, by likening these
protuberances/indentations to solid hemispheres (protuberances) or
hemispherical voids (indentations). It goes without saying that this is an average
size and that protuberances/indentations of more random shape, for example
more elongated, are included.
These protuberances and/or indentations may also have a height (in the
case of protuberances) or a depth (in the case of indentations) of between 5 and
100 nm, especially between 10 and 50 nm. This gives an indication of the
maximum value for each protuberance/indentation whose size it is desired to
determine.
One way of measuring these dimensions consists in carrying out
measurements based on photographs taken by scanning electron microscopy
(SEM).
Such photographs can also be used to determine the distribution of these
indentations/protuberances per unit area of the substrate. It is thus possible to
have a number of protuberances/indentations for this first coating of between5
and300 per µm2, especially between20 and 200 per µm2, of coated substrate.
One way of measuring these hydrophilicity-enhancing
protuberances/indentations consists in measuring the rms roughness expressed
in nm. This first coating may thus have an rms roughness of between 4 and
12 nm, especially between 5 and 10 nm, and more particularly between 6 and
9 nm.
The second coating, that exhibiting photocatalytic properties, is
preferably thin, that is to say it has a thickness of at most 10 nm, especially a
thickness of at most 8 or 5 or 3 nm, in the regions where it actually overlaps the
first coating. In fact, it may be so thin as to tend toward the detection limits of
the machines normally used to evaluate interferential layer thicknesses. As
mentioned above, the term "coating" is to be taken in its broadest sense insofar
as this coating may be discontinuous, in the form of at least partly discrete
islands, or so porous as to be considered as discontinuous. It is in fact just this
point that is surprising in the invention, that such a coating, despite its very
"tenuous" character, does provide a certain functionality.
Its presence may, perhaps more justifiably, be quantified not so much by
a thickness value but by the amount of material deposited per unit area of
substrate (any discontinuity in the coating is thus taken into account). In the
case here, this amount may advantageously be at most 10 micrograms per cm2,
especially at most 5 or 3 micrograms per cm2. It is preferable for this to be
within the range from about 0.5 to 3 micrograms per cm2, i.e. really very small
amounts (compared with the amount of material per cm2 provided, for example,
by an SiOC-based hydrophilic first coating with a thickness of around fifty
nanometers, which is already about 10 micrograms per cm2 of substrate for an
SiOC material, albeit less dense than bulk TiO2).
Advantageously, this second coating will therefore be able to let the first
coating "breathe" and allow at least part of the antisoiling activity associated
with its hydrophilicity, that it would have in its absence, to be retained.
The second coating is preferably deposited by sol-gel, or by CVD-type
pyrolysis or by a vacuum technique of the sputtering type.
From an industrial standpoint, it is most beneficial to produce this double
coating continuously, by depositing the first coating and then the second by
chemical vapor deposition on a ribbon of float glass, for example, when glass
substrates are involved.
Advantageously, the second coating is essentially based on optionally
doped titanium oxide, consisting of grains or crystallites with a diameter of
between 0.5 and 100 nm, especially between 2 and20 nm. Here again the term
"diameter" is to be taken in the broad sense - it is more a determination of the
size of the crystallites. The shape of the grains may approach that of a sphere or
have an elongate shape of the rice grain type, or have a completely random
shape. These grains/crystallites may be at least partly touching. They may also
exhibit some cohesion owing to amorphous oxide that will incorporate/bind
these crystallized grains.
Preferably, the ratio of the diameter of the protuberances on the external
surface of the first (hydrophilic) coating to that of the grains or crystallites of
the second (photocatalytic) coating is at least 2, especially at least 4, 5 or even
at least 10.
Advantageously, the second coating will "follow" the roughness of the
first, if there is any roughness, and even sometimes enhance it. Thus, the rms
surface roughness in nm of the substrate coated with the hydrophilic first
coating and with the photocatalytic second coating will be between 4 and
15 nm, especially between 5 and 12 nm, more particularly between 7 and 10 nm.
Taking an embodiment described above in which the external surface of
the first coating is provided with indentations/protuberances and in which the
second coating comprises grains/crystallites, these grains/crystallites may be
placed between these indentations/protuberances and optionally cover, at least
partly, these indentations/protuberances.
Advantageously, the transparent, especially glass, substrate of the glazing
type, which is provided with the double coating according to the invention, has a
light reflection RL on the coating(s) side of at most 12%, especially at most11%,
under illuminant D65. This thus amounts to a coating of very low reflectivity that
therefore does not penalize the substrate optically, which remains quite
"neutral" optically. Its colorimetric response in reflection may be very slight,
and in neutral colors fairly perceptible (or almost imperceptible) to the eye, and
preferably in the green-blues. This colorimetric response may for example be
quantified by a* and b* values in the (L,a*,b*) colorimetry system, in which
preferably b* is of negative sign. Preferably b* and a* are negative. In absolute
values, a* and b* are preferably less than 5 or 4 or 3.
Advantageously, the combination of the first and second coatings has a
photocatalytic activity characterized by a rate of degradation of palmitic acid of
at least 5 nm/h, especially at least 10 nm/h when exposed to appropriate
radiation, especially ultraviolet radiation. The conditions for the test measuring
this rate of degradation will be explained in detail during the subsequent
description of the examples.
Also advantageously, the combination of the two coatings exhibits
hydrophilicity characterized by a water contact angle of at most 10° or 5°, with
or without exposure to radiation in the ultraviolet or the visible.
The subject of the invention is also the application of the substrates
according to the invention, especially those that are essentially transparent, to
the manufacture of "self-cleaning" glazing that can provide, simultaneously,
antisoiling, antifogging and anticondensation behavior. This may be glazing for
buildings of the double-glazing type, vehicle windows of the windshield, rear
window, sunroof, side window or rear-window type. They may also be windows
for trains, aircraft and ships. It may also be utilitarian glazing, such as aquarium
glass, shop window glass or greenhouse glass, or else glazing used in interior
furnishings or in urban furniture. It may also be glazing used as display screens of
the television, computer or telephone screen type. This type of coating may also
be applied to electrically controllable glazing, such as wire-type or layer-type
heated windows, electrochromic glazing, glazing incorporating a liquid-crystal
film, electroluminescent glazing or photovoltaic glazing.
The substrate according to the invention, apart from its application as
glazing, may be made of any architectural material that can be used for
manufacturing partitions, wall claddings, roofing, flooring, either indoors or
outdoors (metal, wood, stone, cement, concrete, terracotta, ceramic, wall
render, etc.).
The substrate, if instead based on a mineral fibrous material (glass, rock,
silica, etc.), may serve as filtration material or else may be used for false
ceilings, which are not easy to clean.
The invention will be described below with the aid of nonlimiting
examples and figures 1 to 3. All the figures are SEM micrographs of the
examples. In all the examples, the substrate 1 is a silica-soda-lime clear glass
4 mm in thickness (of the type of glass sold by Saint-Gobain Glass France under
the name SGG Planilux).
Example 1
This example relates to the deposition, on the glass 1 again in the form of
a ribbon of float glass, of a first coating 2 based on silicon oxycarbide, denoted
for convenience by SiOC (without prejudging the actual amount of oxygen and
carbon in the coating). This coating 2 was deposited by CVD using Si precursors,
in particular using an SiH4/ethylene mixture diluted in nitrogen, with the aid of a
nozzle placed above and transversely to the ribbon float glass 1 of a flat glass
production line, in the float chamber, when the glass was still at a temperature
of about 600 to 700°C. The coating obtained had a thickness of about 50 nm and
a refractive index of about 1.55. Still on the float line in the float chamber, and
at the same glass temperature, the titanium-oxide-based coating 3 was
deposited, by means of a second nozzle, using titanium isopropylate diluted in
nitrogen. This coating was very thin, probably "noncovering" with respect to the
subjacent coating. Its thickness was determined to be less than 5 nm,
corresponding to an amount of TiO2 of the order of 1 microgram per cm of
substrate. The photographs shown in figures 1a, 1b and 1c relate to this example
1, once the glass ribbon had been cut from the float line: they show, on two
different scales, seen from above and, in the case of figure 1c, obliquely, the
coating 2 that was seeded with pseudo-circular protuberances 4 in the plane of
section, and having a diameter of about 30 to 70 nm. They also show traces of
the coating 3, in the form of grains 5 much smaller in size than the
protuberances 4. These grains lie between the protuberances 4 and perhaps also
at least on these protuberances, but this is difficult to confirm just from these
micrographs. These grains have a size of around 2 to 10 nm.
The glass 1 was then subjected to two series of tests, one a natural aging
test and the other an accelerated aging test.
- Natural aging:
The glass 1 provided with a double coating was exposed on the outside for 6
months at the Charles de Gaulle airport near Paris, so as to be inclined and in
direct contact with rain and sunshine. This is because the environment of an
airport is a very good test environment as it is a highly polluted atmosphere,
especially polluted with higher hydrocarbon contents in the air than elsewhere.
After 6 months, it was found that the glass retained a clean and wetting
appearance: the glass treated according to the invention therefore has actual
"self-cleaning" properties, even under environmental conditions that are neither
very sunny nor very rainy, as encountered in the Paris region. It is therefore
capable of ridding itself of organic soiling, even with a very thin if not
discontinuous photocatalytic coating 3. In addition, it remains hydrophilic. For
comparison, the uncoated glass of untreated SGG Planilux type, subjected to
exactly the same environmental conditions, loses its wetting character after 15
days of exposure, with visible traces of droplets and dust.
- Accelerated aging:
The photocatalytic activity of the treated glass according to example 1
was firstly measured by what is called the palmitic acid test. This test consists in
depositing, on 15 cm2 of the surface of the treated glass, by spraying, a palmitic
acid solution (8 grams of acid per 1 l of chloroform) with a glass/spray distance
of 20 cm, on a vertical substrate in 3 to 4 successive passes. Next, the glass is
weighed in order to determine the thickness in nanometers of palmitic acid
deposited (by weighing the glass specimen before deposition of the palmitic
acid). The glass was then exposed to UVA with an intensity of about 30 W/m2.
The photocatalytic activity was then calculated as the rate of disappearance
v (in nm/h) of palmitic acid, this rate being defined as follows:
v(nm/h) = palmitic acid thickness (nm) / (2 x t ½ disappearance (h)).
The value v for the treated surface of the treated glass was initially about
10 nm/h. Its water contact angle was 5 - this surface was therefore strongly
hydrophilic and also photocatalytic.
• Variable environment test
This test was carried out according to the NF P 78 451 standard. It
involves subjecting the glass to 4 cycles per 24 hours, with hold periods of 2
hours at 55°C and 95% relative humidity, then 1 hour at -15°C, with transitions
lasting 1 hour 30 minutes. The water contact angle was measured every 10 days
as follows: the glass was exposed for 20 minutes to UV and then stored in the
dark for 72 hours. The measurement was then carried out, this being an average
of three measurements on three different drops.
After 10 days of testing, the water contact angle, which was 5° initially,
increased to 10°. Then, after 20 days, the water contact angle dropped to 5°.
This 5° value then remained approximately constant for up to 55 days. These
measurements therefore merely prove that the hydrophilicity of the treated
glass is indeed preserved over time, this hydrophilicity probably being a
combination of the hydrophilicity of the first and of the second coating.
• High humidity test
This test was carried out according to the EN 1096-2 standard. It involves
subjecting the glass to a temperature of 40°C in a chamber saturated with
moisture, with a relative humidity of greater than 95%, with water having a
conductivity of less than 30 µS and a pH of greater than 5 running over the
treated face of the glass. The treated glass having undergone this test was then
exposed for 10 and 20 days to UV and then stored for 72 hours in the dark, as in
the previous test. The water contact angle measurement was also an average of
three measurements. After 10 days, the water contact angle was 10° and after
20 days it had dropped back down to 5°.
• Neutral salt fog test
This test was carried out according to the EN 1036 standard. It involves
placing the glass in a chamber at 35°C with a fine spray of hot (35°C) neutral
(5% NaCl in water) brine, the treated surface being exposed to this fog. The
water contact angle of the treated surface was again measured under the same
conditions as the previous two tests. The contact angle remained at 5° for 55
days.
Example 2
This example is similar to example 1, but the coating 3 was "thicker", by
sputtering a larger amount of titanium oxide precursor: in the case of
example 2, the amount of TiO2 deposited on the coating 2 was about 2.3
micrograms per cm2 of substrate. The SEM photographs of figures 2a, 2b and 2c
show the treated surface seen from above and obliquely, on two different
scales: they show a structure similar to that of example 1. The initial
photocatalytic activity of the treated surface was 20 nm/h and its initial water
contact angle was 5°. After 15 days of the variable environmental test, the
water contact angle was 10°. It was even 18° after 15 days of high-humidity
testing (same conditions as in example 1). Everything occurs as if the presence in
larger quantity of the photocatalytic TiO2 increases the photocatalytic activity of
the coating by a factor of 2, but there should be a reason (not yet explained)
why the hydrophilicity decreases slightly after accelerated environmental aging.
However, it should be noted that a hydrophilic coating is still present, within the
meaning of the term "hydrophilic", with a water contact angle of at most 20°
after having undergone the tests.
For comparison, figure 3 shows an SEM photograph seen from above of a
glass coated only with the SiOC coating 2: the protuberances may again be seen,
but the TiO2 grains lying between these protuberances are no longer present.
WE CLAIM
1. A substrate (1) substantially transparent with improved functionality
adaptable in buildings, vehicles, urban furnitures, and domestic electrical
appliances, characterized in that it is provided on at least part of its
surface with a first coating (2) comprising a layer or several stacked layers
based on an at least partly oxidized derivative of silicon, selected from
silicon dioxide, substoichiometric silicon oxides and a silicon oxycarbide,
oxynitride or oxycarbonitride, said first coating (2) exhibiting hydrophilicity
and being surmounted by a second coating (3) having photocatalytic
properties, which comprises at least partly crystallized titanium oxide, said
second coating (3) having a discontinuous or permeable structure.
2. The substrate as claimed in claim 1, comprising glass or polymer,
intended to serve as glazing, for example, a display screen.
3. The substrate as claimed in claim 1, comprising ceramic or glass-ceramic
adaptable in domestic electrical appliances.
4. The substrate as claimed in claim 1, comprising architectural material for
example, roof tile, architectural concrete, a wall render, concrete slab cr
block, material of cementitious composition, terracotta, slate, stone, or
metal surface.
5. The substrate as claimed in claim 1, comprising fibrous mineral materials
for example, glass-insulation wool or textile glass yarns.
6. The substrate as claimed in claim 1, wherein said substrate is substantially
transparent, flat or curved, of the impressed glazing type.
7. The substrate (1) as claimed in one of the preceding claims, wherein the
refractive index of the first coating (2) is between 1.45 and 1.80,
preferably 1.50 and 1.75, more preferably 1.55 to 1.68.
8. The substrate (1) as claimed in one of the preceding claims, wherein the
first coating (2) is deposited by sol-gel or by pyrolysis, in particular
chemical vapor deposition (CVD) or by a vacuum technique of the
sputtering type.
9. The substrate (1) as claimed in one of the preceding claims, wherein the
first coating (2) has a minimum thickness of 5 nm, preferably between 10
and 200 nm, and more preferably between 30 and 120 nm.
10.The substrate (1) as claimed in one of the preceding claims, wherein the
first coating (2) is rough and has an external surface with one cf
nanoscale protuberances and indentations, or a combination of both.
11.The substrate (1) as claimed in claim 6, wherein the first coating (2) has
an external surface exhibiting protuberances some of the protuberances
are not touching each other.
12.The substrate (1) as claimed in claim 10, or claim 11, wherein the first
coating (2) has, on the external surface, one of protuberances and
indentations, or a combination of both with a diameter of between 5 and
300 nm, preferably between 50 and 100 nm.
13.The substrate (1) as claimed in claims 10 to 11, wherein the first coating
(2) has on the external surface, one of protuberances and indentations or
a combination of both with one of a height and a depth of between 5 and
100 nm, preferably between 10 and 50 nm.
14.The substrate (1) as claimed in claims 10 to 13, wherein the first coating
(2) has an external surface comprising between 5 and 300 protuberances,
preferably between 20 and 200 protuberances per µm2 of the substrate.
15.The substrate (1) as claimed in claims 10 to 14, wherein the first coating
(2) has an rms roughness of between 4 and 12 nm, preferably between 5
and 10 nm and more preferably between 6 and 9 nm.
16.The substrate (1) as claimed in one of the preceding claims, wherein the
second coating (3) has a maximum thickness of 10 nm, preferably 8 or 5
or 3 nm, in the regions of overlap with the first coating (2).
17.The substrate (1) as claimed in one of the preceding claims, wherein the
second coating (3) is based on optionally doped titanium oxide comprising
grains or crystallites with a diameter of between 0.5 and 100 nm,
preferably between 2 and 20 nm.
18.The substrate (1) as claimed in claim 10 and claim 17, wherein the second
coating (3) is based on optionally doped titanium oxide comprising grains
or crystallites, the minimum diameter of the first coating (2) to the
diameter of the grains or crystallites of the second coating (3) is 2,
particularly 4, 5 or 10.
19.The substrate (1) as claimed in one of the preceding claims, wherein the
substrate provided with the first (2) and second (3) coatings has an rms
roughness of between 4 and 15 nm, preferably between 5 and 12 nm and
more preferably between 7 and 10 nm.
20.The substrate (1) as claimed in one of the receding claims, wherein the
second coating (3) follows the roughness of the first coating (2).
21.The substrate as claimed in claim 11 and 17, wherein the
grains/crystallites of the second coating (3) lie between one of the
indentations and protuberances or a combination of both of the external
surface of the first coating (2) and partially cover, said one of the
indentations and protuberances, or a combination of both.
22.The substrate (1) as claimed in one of the preceding claims, wherein the
second coating (3) corresponds to a maximum amount of material of 10
micrograms per cm2 of substrate, preferably 5 or 3 micrograms per cm2
of the substrate, more preferably about 0.5 to 3 micrograms per cm2.
23.The substrate (1) as claimed in cone of preceding claims, wherein the
second coating (3) is deposited by sol-gel, by pyrolysis, preferably
chemical vapor deposition or by a vacuum technique of the sputtering
type.
24.The glass substrate (1) as claimed in one of the preceding claims, wherein
the first and second coatings are deposited by chemical vapor deposition
on a ribbon of float glass.
25.The substrate (1) as claimed in one of the preceding claims, comprising,
when provided with the first and second coatings, a maximum light
reflection on the coating side Ri of 12%, preferably 11%, more preferably
combined with a* and b* values such that 2 26.The substrate (1) as claimed in one of the preceding claims, wherein the
combination of the first and second coatings (2, 3) exhibits photocatalytic
activity characterized by a minimum rate of palmitic acid degradation of 5
nm/h, preferably 10 nm/h.
27.The substrate (1) as claimed in one of the preceding claims, wherein the
combination of the first and second coatings (2, 3) exhibits hydrophilicity
characterized by a water maximum contact angle of 20°, preferably 10°,
or 5° with or without exposure to radiation in the ultraviolet and/or in the
ordinarily visible context.
28. A "self-cleaning", particularly antifogging, anticondensation and
antisoiling, glazing, comprising a substrate as claimed in any of the
preceding claims.
The invention relates to a substrate (1) substantially transparent with
improved functionality adaptable in buildings, vehicles, urban furnitures, and
domestic electrical appliances. It is provided on at least part of its surface
with a first coating (2) comprising a layer or several stacked layers based on
an at least partly oxidized derivative of silicon, selected from silicon dioxide,
substoichiometric silicon oxides and a silicon oxycarbide, oxynitride or
oxycarbonitride, said first coating (2) exhibiting hydrophilicity and being
surmounted by a second coating (3) having photocatalytic properties, which
comprises at least partly crystallized titanium oxide, said second coating (3)
having a discontinuous or permeable structure.

Documents:

1523-kolnp-2004-granted-abstract.pdf

1523-kolnp-2004-granted-claims.pdf

1523-kolnp-2004-granted-correspondence.pdf

1523-kolnp-2004-granted-description (complete).pdf

1523-kolnp-2004-granted-drawings.pdf

1523-kolnp-2004-granted-examination report.pdf

1523-kolnp-2004-granted-form 1.pdf

1523-kolnp-2004-granted-form 18.pdf

1523-kolnp-2004-granted-form 2.pdf

1523-kolnp-2004-granted-form 3.pdf

1523-kolnp-2004-granted-form 5.pdf

1523-kolnp-2004-granted-gpa.pdf

1523-kolnp-2004-granted-letter patent.pdf

1523-kolnp-2004-granted-reply to examination report.pdf

1523-kolnp-2004-granted-specification.pdf

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Patent Number

222880

Indian Patent Application Number

1523/KOLNP/2004

PG Journal Number

35/2008

Publication Date

29-Aug-2008

Grant Date

27-Aug-2008

Date of Filing

12-Oct-2004

Name of Patentee

SAINT-GOBAIN GLASS FRANCE

Applicant Address

LES MIROIRS, 18, AVENUE D'ALSACE, F-92400 COURBEVOIE

Inventors:

#	Inventor's Name	Inventor's Address
1	AZZOPARDI, MARIE-JOSE	52, BOULEVARD DE LA LIBERATION, F-94300 VINCENNES
2	BRASY, SEBASTIEN	35, RUE CHARLES CAILLE F-60150 MONTMACQ

PCT International Classification Number

C03C 17/34

PCT International Application Number

PCT/FR03/01219

PCT International Filing date

2003-04-16

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	02/04774	2002-04-17	France