EP1856004A1 - Substrat für hydrophobe beschichtung - Google Patents
Substrat für hydrophobe beschichtungInfo
- Publication number
- EP1856004A1 EP1856004A1 EP06724895A EP06724895A EP1856004A1 EP 1856004 A1 EP1856004 A1 EP 1856004A1 EP 06724895 A EP06724895 A EP 06724895A EP 06724895 A EP06724895 A EP 06724895A EP 1856004 A1 EP1856004 A1 EP 1856004A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- substrate
- layer
- substrate according
- equal
- mineral layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/42—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating of an organic material and at least one non-metal coating
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/22—Surface treatment of glass, not in the form of fibres or filaments, by coating with other inorganic material
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/20—Materials for coating a single layer on glass
- C03C2217/21—Oxides
- C03C2217/213—SiO2
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/20—Materials for coating a single layer on glass
- C03C2217/21—Oxides
- C03C2217/214—Al2O3
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/20—Materials for coating a single layer on glass
- C03C2217/21—Oxides
- C03C2217/22—ZrO2
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/20—Materials for coating a single layer on glass
- C03C2217/28—Other inorganic materials
- C03C2217/281—Nitrides
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/70—Properties of coatings
- C03C2217/77—Coatings having a rough surface
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2218/00—Methods for coating glass
- C03C2218/10—Deposition methods
- C03C2218/15—Deposition methods from the vapour phase
- C03C2218/152—Deposition methods from the vapour phase by cvd
Definitions
- the present invention relates to a substrate, in particular a glass substrate, comprising a coating comprising at least one mineral layer, intended to receive a hydrophobic organic surface treatment, and relates to said substrate comprising at least one mineral layer and an organic hydrophobic layer.
- hydrophobic properties of a substrate are sought.
- the hydrophobic surface properties of the substrate allow the water to bead and slide more easily leaving less traces of limestone.
- the hydrophobic surface properties allow a better visibility because the drops of water evacuate more quickly.
- Hydrophobic organic treatments are known which can be applied to surfaces exposed to frequent exposure to water. However the lifespan of these treatments is quite limited in time. It is found that the hydrophobic properties decrease after a few months. This requires that organic treatments are reapplied regularly.
- EP 166 363-A discloses a transparent substrate coated with a first layer comprising a metal oxide, in particular TiO 2 , SiO 2 , ZrO 2 , deposited by a sol-gel type method.
- the substrate comprises a second layer based on a fluorinated silica compound.
- the product thus coated has a contact angle with water of 117 °.
- coated substrates known from the state of the art do not generally make it possible to obtain a good resistance in time to the hydrophobic properties eVou are obtained with complex manufacturing processes.
- Some substrates coated with the state of the art have very large roughness (of the order of one micron), which limits the possible applications.
- the subject of the present invention is a substrate, in particular of the glass type, comprising at least one inorganic layer of oxide, nitride or metal oxynite type (1), intended to receive a hydrophobic organic treatment (2).
- Said coated substrate is generally capable of prolonging the life of the organic treatment (2).
- the mineral layer (1) can be deposited by any type of known deposition method, such as pyrolytic methods, for example in the vapor phase (CVD).
- CVD vapor phase
- a particularly advantageous method is the vacuum cathode sputtering technique.
- This method has the advantage over pyrolytic methods of not requiring heating of the substrate and being independent of production lines of floated glass.
- This method also makes it easy to deposit layers composed of mixtures of different metallic elements.
- This method also makes it possible to envisage a variety of substrates such as printed substrates or substrates which have undergone prior treatment such as matting or sanding.
- the mineral layer is preferably deposited on the face opposite to the matted or sandblasted printed face.
- the exposed surface of the layer (1) preferably has a surface roughness Rmax (maximum distance between the maximum peak and the deepest valley) of less than or equal to 17 nm, preferably less than or equal to 13 nm, and more preferably less than or equal to 10 nm and greater than or equal to 0.5, preferably greater than or equal to 1 and more preferably greater than or equal to 1.2 nm and an average difference between peaks Sm preferably greater than or equal to 10 nm, more preferably still greater than or equal to 20 nm, even more preferably 30 nm and preferably less than or equal to 800 nm, more preferably less than 400 nm and even more preferably less than 200 nm.
- Rmax maximum distance between the maximum peak and the deepest valley
- substrates coated with mineral layers whose particular roughness has a Rmax of between 1 and 10 nm and an average difference between peaks (Sm) of between 10 and 250 nm give surprising results over the lifetime of the organic hydrophobic layer deposited on the mineral layer.
- a remarkable advantage of the substrates coated with the mineral layer according to the invention is that it is not necessary to deposit the organic hydrophobic layer immediately after the deposition of the mineral layer. In other words, there is no degradation of the activity of the mineral layer over time.
- This mineral layer remains active and retains its adhesion properties vis-à-vis the hydrophobic layer even if the substrate has been coated with the mineral layer for at least months, even years.
- the average roughness Ra (arithmetic mean deviation from mean line) of the mineral layer is preferably between 0.1 and 9 nm, preferably between 0.2 and 5 nm and even more preferably between 0.3 and 3 nm.
- the roughness values Ra, Rmax and Sm given are the values resulting from a roughness profile measured on a 3 ⁇ m line. These values are measured according to JIS B 0601 and ISO 468-1982. Other values can still be used to define the roughness, for example Rq or RMS (Root-mean square average of the roughness of the mean line), Rp (maximum height of the highest point of roughness above the mean line "), Rv ("max depth or the lowest point of roughness below the mean line ").
- the mineral layer (1) advantageously has an open porosity greater than 10%, preferably greater than 15% and more preferably greater than 20%.
- the mineral layer (1) preferably comprises a metal oxide, nitride or oxynitride whose binding energy is greater than 100 Kcal / mole, preferably greater than 110 Kcal / mole and more preferably greater than 120 Kcal / mole.
- the mineral layer (1) comprises an oxide, nitride or oxynitride of a metal or of several metals preferably chosen from Sn, Zr, Si, Al, Ce, La, Nd, Nb, Ta, and more preferably from Si , Zr and Al and their mixture.
- the mineral sub-layer (1) advantageously has a roughness such that its surface has a columnar structure.
- the mineral layer may be composed of a stack of 2 different sub-layers of different oxide, oxynitride or metal nitride.
- the present invention also relates to a glass substrate comprising at least one inorganic layer of oxide, nitride or metal oxyniture type (1), and comprising a hydrophobic organic layer (2) deposited on the mineral layer (1).
- the substrate thus coated has an angle of contact with the water greater than 70 °, preferably greater than 80 ° and more preferably greater than 90 °.
- the mineral layer has the effect of prolonging the life of the organic coating because the hydrophobic properties of the substrate previously coated with the mineral layer are maintained in time longer than when the organic treatment is directly deposited on the substrate. .
- the contact angle with the water measured after 6 months, is greater for the substrate coated with both the mineral layer (1) and the organic layer (2) than for the substrate coated only with the layer (2).
- the mineral layer has the effect of improving the sliding angle of the organic hydrophobic layer.
- a drop of water of 50 .mu.l was deposited on the substrate disposed horizontally and the substrate was progressively inclined.
- the slip angle is the inclination of the substrate relative to the horizontal, from which the drop of water begins to slide. It was found that the slip angle of the substrate coated with the inorganic layer and the organic layer was smaller than the slip angle of the substrate coated solely with the organic layer. In particular, the slip angle of the substrate coated solely with the organic layer is less than 25 °, preferably less than 20 °.
- various accelerated aging tests can be performed such as immersion of the coated substrate in an alkaline medium (0.1 N NaOH), immersion in an acid medium (H 2 SO 4 0.1N), the test cleveland (exposure of the substrate coated with damp vapors from a demineralised water tank heated to 50 0 C), the wet fog exposure test (40 0 C, 98% relative humidity), the test of UV exposure (60 ° C., UVA340 lamp).
- an alkaline medium 0.1 N NaOH
- immersion in an acid medium H 2 SO 4 0.1N
- the test cleveland exposure of the substrate coated with damp vapors from a demineralised water tank heated to 50 0 C
- the wet fog exposure test 40 0 C, 98% relative humidity
- the test of UV exposure 60 ° C., UVA340 lamp
- the contact angle with the water remains greater than 70 ° for a longer period for the substrate coated with the layers (1) and (2) relative to the substrate coated solely with the layer (2).
- the coated substrate is preferably neutral in transmission, these colorimetric indices (CIELAB) a * and b * are preferably between -10 and +3, more preferably between -5 and +2 and even more preferably between -5 and +2. 3 and +1.
- CIELAB colorimetric indices
- the substrate may be chosen from any type of substrate for which hydrophobic properties are desired, in particular substrates of the glass, glass-ceramic or metallic type.
- Preferred glass substrates are, for example, soda-lime glass that is clear, colored, printed, matt or sanded.
- the coated substrate can in particular be used for the manufacture of shower doors, for the formation of automotive glazing (mainly windshields), or architectural glazing (generally double glazing) whether for the outer or inner side of the building.
- automotive glazing mainly windshields
- architectural glazing generally double glazing
- FIGS. 1 to 4 representing the roughness profiles of the examples according to the invention 2 to 5 respectively.
- Each figure shows a front view of an area of 9 ⁇ m 2 of the sample and a graph showing the profile along a 3 ⁇ m line.
- the left column shows the roughness values according to 1 line and the right column takes the average values for the whole surface of 9 ⁇ m 2 .
- the samples are previously washed in the machine. They are pickled by annealing (15 min., At 250 0 C) to remove any trace of organic matter. The samples are then polished with cerium oxide and rinsed and ironed in a washing machine. a) 10 ml of an organic polydimethylsiloxane treatment (Daryl®) are applied to the surface of the samples with the aid of a paper, by exerting circular motions. The product is allowed to act for 24 hours at room temperature. Shorter times could be expected with higher temperatures.
- Daryl® organic polydimethylsiloxane treatment
- a 5 nm thick ZrO 2 layer is deposited by vacuum magnetic sputtering with a Zr metal target in an argon and oxygen atmosphere on clear soda-lime glass samples.
- the coated glass has a neutral coloration in transmission.
- a 5 nm Si (Al) N x layer is deposited by vacuum magnetic sputtering with a metal Si target having 8% Al in a nitrogen and argon atmosphere.
- the coated glass has a neutral coloration in transmission.
- a 25 nm layer of Si and Zr oxynitride is deposited by vacuum magnetic co-sputtering with a Zr metal target and a Zr Si (Al 8%) metal target in a mixed argon, oxygen atmosphere. and nitrogen.
- the coated glass has a neutral coloration in transmission.
- a 5 nm layer of Si and Zr oxynitride is deposited as in the previous point.
- the coated glass has a neutral coloration in transmission.
- One of the organic treatments (a to c) above is deposited, in the same manner as in Comparative Example 1 above, on each of the glasses coated with one of the mineral layers (2 to 5).
- the hydrophobic properties of the coated substrates are measured by the contact angle with water.
- the angle of contact with the water is measured initially and after accelerated aging tests in alkaline medium and in acid medium. Sliding angles are also measured initially for water drops of 50 ⁇ L.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06724895A EP1856004A1 (de) | 2005-02-28 | 2006-02-27 | Substrat für hydrophobe beschichtung |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05101496 | 2005-02-28 | ||
EP06724895A EP1856004A1 (de) | 2005-02-28 | 2006-02-27 | Substrat für hydrophobe beschichtung |
PCT/EP2006/060295 WO2006089964A1 (fr) | 2005-02-28 | 2006-02-27 | Substrat pour revêtement hydrophobe |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1856004A1 true EP1856004A1 (de) | 2007-11-21 |
Family
ID=34938831
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP06724895A Withdrawn EP1856004A1 (de) | 2005-02-28 | 2006-02-27 | Substrat für hydrophobe beschichtung |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP1856004A1 (de) |
WO (1) | WO2006089964A1 (de) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1765740B1 (de) | 2004-07-12 | 2007-11-07 | Cardinal CG Company | Wartungsarme beschichtungen |
JP5129975B2 (ja) | 2006-04-11 | 2013-01-30 | 日本板硝子株式会社 | 向上した低保守特性を有する光触媒コーティング |
US20080011599A1 (en) | 2006-07-12 | 2008-01-17 | Brabender Dennis M | Sputtering apparatus including novel target mounting and/or control |
EP2261186B1 (de) | 2007-09-14 | 2017-11-22 | Cardinal CG Company | Pflegeleichte beschichtungstechnologie |
EP3541762B1 (de) | 2016-11-17 | 2022-03-02 | Cardinal CG Company | Statisch-dissipative beschichtungstechnologie |
FR3063288B1 (fr) * | 2017-02-28 | 2019-03-22 | Saint-Gobain Glass France | Article pour piece humide comprenant un vitrage hydrophobe |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0649597B2 (ja) * | 1989-08-24 | 1994-06-29 | トヨタ自動車株式会社 | 撥水性ガラス |
FR2722493B1 (fr) * | 1994-07-13 | 1996-09-06 | Saint Gobain Vitrage | Vitrage hydrophobe multicouches |
JP3498881B2 (ja) * | 1996-05-27 | 2004-02-23 | セントラル硝子株式会社 | 撥水性ガラスの製法 |
DE10018671C2 (de) * | 2000-04-14 | 2002-09-26 | Nanogate Technologies Gmbh | Verfahren zur Erzeugung einer hydrophoben Oberfläche von Gegenständen aus silikatkeramischen Werkstoffen sowie Gegenstand mit einer hydrophoben Oberfläche |
DE10063739B4 (de) * | 2000-12-21 | 2009-04-02 | Ferro Gmbh | Substrate mit selbstreinigender Oberfläche, Verfahren zu deren Herstellung und deren Verwendung |
KR20040052516A (ko) * | 2001-11-08 | 2004-06-23 | 니혼 이타가라스 가부시키가이샤 | 피막 피복 물품, 및 이것을 이용한 기능성 피막 피복 물품 |
-
2006
- 2006-02-27 WO PCT/EP2006/060295 patent/WO2006089964A1/fr active Application Filing
- 2006-02-27 EP EP06724895A patent/EP1856004A1/de not_active Withdrawn
Non-Patent Citations (1)
Title |
---|
See references of WO2006089964A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2006089964A1 (fr) | 2006-08-31 |
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Legal Events
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17P | Request for examination filed |
Effective date: 20070928 |
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AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR |
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17Q | First examination report despatched |
Effective date: 20080227 |
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DAX | Request for extension of the european patent (deleted) | ||
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
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18D | Application deemed to be withdrawn |
Effective date: 20080909 |