US20120064240A1 - Transparent aqua-based nano sol-gel composition and method of applying the same - Google Patents

Transparent aqua-based nano sol-gel composition and method of applying the same Download PDF

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US20120064240A1
US20120064240A1 US13/297,696 US201113297696A US2012064240A1 US 20120064240 A1 US20120064240 A1 US 20120064240A1 US 201113297696 A US201113297696 A US 201113297696A US 2012064240 A1 US2012064240 A1 US 2012064240A1
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transparent
hours
glass
gel
aqua
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Wen-Chuan Liu
Chien-Kuo Huang
Shiaw-Tseh Chiang
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ONID Tech (Shanghai) Corp
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    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/006Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character
    • C03C17/007Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character containing a dispersed phase, e.g. particles, fibres or flakes, in a continuous phase
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/006Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character
    • C03C17/008Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character comprising a mixture of materials covered by two or more of the groups C03C17/02, C03C17/06, C03C17/22 and C03C17/28
    • C03C17/009Mixtures of organic and inorganic materials, e.g. ormosils and ormocers
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/22Surface treatment of glass, not in the form of fibres or filaments, by coating with other inorganic material
    • C03C17/23Oxides
    • C03C17/25Oxides by deposition from the liquid phase
    • C03C17/256Coating containing TiO2
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/28Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
    • C03C17/30Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with silicon-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/043Improving the adhesiveness of the coatings per se, e.g. forming primers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/06Coating with compositions not containing macromolecular substances
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D4/00Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • C09D4/06Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/16Antifouling paints; Underwater paints
    • C09D5/1606Antifouling paints; Underwater paints characterised by the anti-fouling agent
    • C09D5/1612Non-macromolecular compounds
    • C09D5/1618Non-macromolecular compounds inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/16Antifouling paints; Underwater paints
    • C09D5/1656Antifouling paints; Underwater paints characterised by the film-forming substance
    • C09D5/1662Synthetic film-forming substance
    • C09D5/1675Polyorganosiloxane-containing compositions
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10Optical coatings produced by application to, or surface treatment of, optical elements
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10Optical coatings produced by application to, or surface treatment of, optical elements
    • G02B1/18Coatings for keeping optical surfaces clean, e.g. hydrophobic or photo-catalytic films
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C2217/00Coatings on glass
    • C03C2217/40Coatings comprising at least one inhomogeneous layer
    • C03C2217/425Coatings comprising at least one inhomogeneous layer consisting of a porous layer
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C2217/00Coatings on glass
    • C03C2217/40Coatings comprising at least one inhomogeneous layer
    • C03C2217/43Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
    • C03C2217/46Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase
    • C03C2217/47Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase consisting of a specific material
    • C03C2217/475Inorganic materials
    • C03C2217/477Titanium oxide
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C2217/00Coatings on glass
    • C03C2217/70Properties of coatings
    • C03C2217/71Photocatalytic coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2369/00Characterised by the use of polycarbonates; Derivatives of polycarbonates

Definitions

  • the present invention as disclosed herein and further defined by the claims relates to a transparent aqua-based nano sol-gel composition and a method of applying the same to transparent substrates without decreasing the visible light and sunlight transmittance thereof.
  • the transparent aqua-based nano sol-gel can be applied to a surface of a transparent substrate to form a porous film which will not reduce the visible light and sunlight transmittance of the transparent substrate and will impart a self-cleaning function to the transparent substrate.
  • the transparent aqua-based nano sol-gel composition comprises a transparent aqua-based zeolite sol-gel having a particle size of less than 100 nm, a polysiloxane derivate, a surfactant, a transparent aqua-based photocatalytic sol-gel of titanium dioxide having a particle size of less than 100 nm, and deionized water.
  • Transparent substrates are always used as protection covers of solar energy products and lighting lamps, and the transmittance of the transparent substrates to lights plays an important role to the total efficiency of these products.
  • glass is used as the transparent substrate, and the reflectivity of glass substrate to light is about 8%. If the reflectivity of glass substrate can be reduced, the transmittance of glass substrate can be increased. In addition, the contaminants or stains on the glass substrates will remarkably reduce the transmittance to light, hence it is desirable to impart the self-cleaning function to the glass substrates and to increase the transmittance of glass substrate to light.
  • the anti-reflective glass capable of increasing the transmittance to light and the photocatalyst-coated glass with self-cleaning function have been put into mass production.
  • the photocatalyst-coated glass is generally coated with titanium dioxide (TiO 2 ) having high refractive index, and the visible light and sunlight reflectivity thereof is about 12% and hence the transmittance thereof is reduced.
  • the application of coating film to the glass is mostly conducted by processes such as vacuum sputtering, physical vapor deposition, chemical vapor deposition, etc. using low pressure vacuum equipment which is very expensive.
  • the functional glass is too expensive to be accepted by the general consuming public. It is therefore important to develop the functional glass with low cost.
  • U.S. Pat. No. 5,216,542 discloses a multilayer coating structure upon transparent substrate.
  • the top layer of the multilayer structure is silicon dioxide (SiO 2 ) and has a refractive index of 1.46 at a wavelength of 550 nm, which has anti-reflection effect but no self-cleaning property.
  • U.S. Pat. No. 5,105,310 discloses a multilayer anti-reflection coating upon transparent substrate.
  • the top layer of the multilayer structure is silicon dioxide (SiO 2 ) and has a refractive index of 1.46 at a wavelength of 550 nm, which has anti-reflection effect but no self-cleaning property.
  • U.S. Pat. No. 5,147,125 discloses a multilayer anti-reflection coating upon transparent substrate.
  • the top layer of the multilayer structure is Magnesium Fluoride (MgF 2 ) and has a refractive index of 1.38 at a wavelength of 550 nm, which has anti-reflection effect but no self-cleaning property.
  • MgF 2 Magnesium Fluoride
  • China Patent No. CN1447133A discloses an anti-reflection layer which is transparent, conductive and can increase the transmittance to light.
  • the top layer of the multilayer is an ITO layer (Indium Tin Oxide), which has anti-reflection effect but no self-cleaning property.
  • China Patent No. CN1101353C discloses self-cleaning glass and its manufacturing method.
  • the titanium dioxide layer is deposited on the surface of glass by a sputtering process which is expensive.
  • the coated glass has self-cleaning property and its refractive index is about 2.5 ⁇ 2.7. However, the coated glass with high refractive index will remarkably reduce the transmittance to light.
  • China Patent No. CN1579981A discloses photocatalyst-coated glass and its manufacturing method.
  • the titanium dioxide layer is deposited on the surface of glass by a vacuum sputtering process which is expensive.
  • the coated glass has self-cleaning property and its refractive index is about 2.5 ⁇ 2.7. However, the coated glass with high refractive index will remarkably reduce the transmittance to light.
  • China Patent No. CN1660955A discloses a spray agent for nano photocatalyst-coated glass and its preparation method.
  • the nano photocatalyst liquid consists of titanium dioxide nanopowder and other nanopowder dispensed in the dispersants.
  • the nano photocatalyst liquid is turbid and will reduce the transmittance to light after coated on the glass.
  • Taiwan Patent No. 00313630 discloses a method of photocatalytically making the surface of a base material ultrahydrophilic, a base material having ultrahydrophilic and photocatalytic surface, and a process for producing said material.
  • This invention only describes the applications of photocatalyst to different substrates; however, no discussion is made regarding the optical performance for the coated substrates.
  • parts of the method/process of this invention require the use of 900° C. and such a high temperature is not convenient for all types of substrates.
  • the main objective of the present invention is to provide a transparent aqua-based nano sol-gel composition applying to transparent substrates without decreasing the visible light and sunlight transmittance thereof.
  • the transparent aqua-based nano sol-gel can be applied to a surface of a transparent substrate to form a porous film which will not reduce the visible light and sunlight transmittance of the transparent substrate and will impart a self-cleaning function to the transparent substrate.
  • the transparent aqua-based nano sol-gel composition comprises a transparent aqua-based zeolite sol-gel having a particle size of less than 100 nm, a polysiloxane derivate, a surfactant, a transparent aqua-based photocatalytic sol-gel of titanium dioxide having a particle size of less than 100 nm, and deionized water.
  • the test method for the self-cleaning property refers to “Test Method for Self-Cleaning Performance of Photocatalytic Building Materials” published by the Taiwan Photocatalyst Industry Association.
  • the process of the test method comprises the steps of applying the oleic acid to the photocatalytic substrate and making the contact angle of droplet on the substrate higher than 30°. After exposing the substrate under the UVA light with intensity of 1 mW/cm 2 or above for 24 hours, the oleic acid applied to the photocatalytic surface can be decomposed and the contact angle of droplet on the substrate is less than 15°.
  • the present invention can reduce the high production costs of the conventional art, simplify the production process, lower the production temperature, save energy, lower the production cost, and is environmental friendly.
  • the present invention relates to a transparent aqua-based nano sol-gel composition and a method of applying the same to transparent substrates without decreasing the visible light and sunlight transmittance thereof.
  • the method of applying the transparent aqua-based nano sol-gel composition to transparent substrates comprises the steps of:
  • preparing the transparent aqua-based sol-gel a transparent aqua-based zeolite sol-gel having a particle size of less than 100 nm, a polysiloxane derivate, a surfactant, a transparent aqua-based photocatalytic sol-gel of titanium dioxide having a particle size of less than 100 nm, and deionized water are well mixed and filtered to obtain the transparent aqua-based sol-gel.
  • the transparent aqua-based nano sol-gel is applied to a surface of a transparent substrate evenly to form a transparent coating film and then the coating film is cured by a predetermined curing process so that the transparent coating film can adhere to the surface of the substrate more rigidly and reliably.
  • the dry film thickness of the finished transparent aqua-based coating film is between 40 ⁇ 350 nm.
  • the transparent aqua-based nano sol-gel composition according to the present invention is characterized by comprising: a transparent aqua-based zeolite sol-gel in a solid content of 0.1 ⁇ 15.0 wt %, preferably 0.1 ⁇ 10 wt %, and more preferably 0.1 ⁇ 5 wt %; a polysiloxane derivate in a solid content of 0.0001 ⁇ 10.0 wt %, preferably 0.001 ⁇ 17 wt %, and more preferably 0.01 ⁇ 3 wt %, wherein the polysiloxane derivate is selected from the group consisting of methyltrimethoxysilane, methyltriethoxysilane, ethyltributoxysilane, trimethyldiethyoxysilane, dimethoxymethylphenylsilane, triethoxypropylsilane, tripropoxypropylsilane and tributoxymethylsilane; a non-ionic surfactant in
  • the transparent aqua-based nano sol-gel composition is evenly applied to the surface of the transparent substrate with any wet coating method selected from a roll coating method, a wipe coating method, a brush coating method, a dip coating method, a spray coating method, a spin coating method or a sprinkle coating method, which can be carried out to coat one side or both sides of the transparent substrate.
  • the “coating film is cured by a predetermined curing process” mentioned above refers to curing the coating film with natural air drying for 24 hours or above, or heating at a temperature of 450° C. or below for 5 minutes or above.
  • the transparent substrate referred to in the present invention can be selected from the group consisting of glass and plastic substrates, including transparent glass, transparent polycarbonate resins, transparent polymethacrylate resins, transparent polystyrene resins and transparent epoxy resins.
  • the transparent coating film formed upon transparent substrates according to the present invention possesses self-cleaning property under light irradiation, and the light can be either sun light or artificial light.
  • FIG. 1 shows the transparent substrate and the coating film according to the present invention.
  • FIG. 2 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 1.
  • FIG. 3 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 2.
  • FIG. 4 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 3.
  • FIG. 5 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 4.
  • FIG. 6 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 5.
  • FIG. 7 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 6.
  • FIG. 8 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 7.
  • FIG. 9 shows the light transmittance comparison for transparent polycarbonate resins substrate before coating and after coating according to Example 8.
  • FIG. 10 shows the light transmittance comparison for transparent polymethacrylate resins substrate before coating and after coating according to Example 9.
  • FIG. 11 shows the light transmittance comparison for transparent polystyrene resins substrate before coating and after coating according to Example 10.
  • FIG. 12 shows the light transmittance comparison for transparent epoxy resins substrate before coating and after coating according to Example 11.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 0.1 wt % solid content of a transparent aqua-based zeolite sol-gel, 0.0001 wt % solid content of methyltrimethoxysilane as the polysiloxane derivate, 0.0001 wt % solid content of polyoxyethylene p-octylphenol ether as the non-ionic surfactant, 0.1 wt % solid content of the transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a dip coating method.
  • the surface of glass ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass ( 1 ) by a dip coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 40-50 nm on the surface of the glass after cured with nature air drying for 24 hours.
  • T % A comparison of the transmittance (T %) at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 2 . It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3 A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°.
  • Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 67° indicating that the surfaces of the pieces of glass were contaminated by oleic acid.
  • the two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period.
  • the results are shown in Table 1.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated glass possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 2. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 15.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 10 wt % solid content of methyltriethoxysilane as the polysiloxane derivate, 10 wt % solid content of polyoxyethylene p-octyl laurate as the non-ionic surfactant, 2 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a spin coating method.
  • the surface of glass ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass ( 1 ) by a spin coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 120-132 nm on the surface of the glass after cured with nature air drying for 24 hours.
  • FIG. 3 A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 3 . It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3 A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°.
  • Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 65° indicating that the surfaces of the pieces of glass were contaminated by oleic acid.
  • the two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period.
  • the results are shown in Table 3.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated glass possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 4. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 2.0 wt % solid content of transparent aqua-based zeolite sol-gel, 3.0 wt % solid content of ethyltributoxysilane as the polysiloxane derivate, 2.0 wt % solid content of polyoxyethylene sorbitol laurate as the non-ionic surfactant, 0.7 wt % solid content of transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a wipe coating method.
  • the surface of glass ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass ( 1 ) by a wipe coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 95-105 nm on the surface of the glass after cured with nature air drying for 24 hours.
  • FIG. 4 A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 4 . It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3 A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°.
  • Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 68° indicating that the surfaces of the pieces of glass were contaminated by oleic acid.
  • the two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period.
  • the results are shown in Table 5.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated glass possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 6. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 5.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 6.0 wt % solid content of trimethyldiethyoxysilane as the polysiloxane derivate, 8.0 wt % solid content of polyoxyethylene oleoyl ether as the non-ionic surfactant, 1.0 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a roll coating method.
  • the surface of glass ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass ( 1 ) by a roll coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 125-146 nm on the surface of the glass after cured with nature air drying for 24 hours.
  • a comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 5 . It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3 A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°.
  • Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 64° indicating that the surfaces of the pieces of glass were contaminated by oleic acid.
  • the two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period.
  • the results are shown in Table 7.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated glass possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 8. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 10.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 10.0 wt % solid content of dimethoxymethylsilane as the polysiloxane derivate, 2.0 wt % solid content of polyoxyethylene stearyl ether as the non-ionic surfactant, 1.5 wt % solid content of transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a spray coating method.
  • the surface of glass ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass ( 1 ) by a spray coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 140-170 nm on the surface of the glass after cured with nature air drying for 24 hours.
  • FIG. 6 A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 6 . It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3 A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°.
  • Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 69° indicating that the surfaces of the pieces of glass were contaminated by oleic acid.
  • the two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period.
  • the results are shown in Table 9.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated glass possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 10. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 7.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 1.0 wt % solid content of methyltributoxysilane as the polysiloxane derivate, 5.0 wt % solid content of oleic diethanol amide as the non-ionic surfactant, 0.8 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a brush coating method.
  • the surface of glass ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass ( 1 ) by a brush coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 136-164 nm on the surface of the glass after cured with nature air drying for 24 hours.
  • FIG. 7 A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 7 . It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3 A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°.
  • Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 66° indicating that the surfaces of the pieces of glass were contaminated by oleic acid.
  • the two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period.
  • the results are shown in Table 11.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated glass possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 12. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 3.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 3.0 wt % solid content of propyltripropoxysilane as the polysiloxane derivate, 2.0 wt % solid content of polyoxyethylene sorbitan laurate as the non-ionic surfactant, 0.6 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a sprinkle coating method.
  • the surface of glass ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass ( 1 ) by a sprinkle coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 65-80 nm on the surface of the glass after cured with nature air drying for 24 hours.
  • FIG. 8 A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 8 . It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3 A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°.
  • Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 64° indicating that the surfaces of the pieces of glass were contaminated by oleic acid.
  • the two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period.
  • the results are shown in Table 13.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated glass possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 14. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • Step 1 A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 12.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 0.1 wt % solid content of propyltriethoxysilane as the polysiloxane derivate, 0.1 wt % solid content of polyoxyethylene p-octyl laurate as the non-ionic surfactant, 1.8 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of a polycarbonate substrate having the thickness of 5 mm by a brush coating method.
  • the surface of the polycarbonate substrate was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the polycarbonate substrate ( 1 ) by a brush coating method, and a transparent coating film ( 2 ) was formed in a thickness of about 40-60 nm on the surface of the polycarbonate substrate after cured with nature air drying for 24 hours.
  • a comparison of the transmittance at different wavelengths between the coated polycarbonate substrate and uncoated polycarbonate substrate is shown in FIG. 9 . It is obvious that the transmittance of the coated polycarbonate substrate is higher than that of the uncoated polycarbonate substrate.
  • Step 3 A comparison of the self-clean property between the coated polycarbonate substrate and the uncoated polycarbonate substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated and uncoated polycarbonate substrates were firstly cleaned, and then the contact angle of a droplet on the two polycarbonate substrates was measured, which was about 65°.
  • Oleic acid was evenly spread upon the surfaces of the coated and uncoated polycarbonate substrates to simulate the contamination on the polycarbonate substrate, and then the contact angle of a droplet was again measured, which was now about 75° indicating that the surfaces of the polycarbonate substrates were contaminated by oleic acid.
  • the two contaminated polycarbonate substrates were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated polycarbonate substrates were measured at each period. The results are shown in Table 15. The lower contact angle indicates a better self-cleaning property. Also, the uncoated polycarbonate substrate possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of polycarbonate substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example.
  • the coated polycarbonate substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3.
  • the results are shown in Table 16. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the polycarbonate substrates will not decrease the visible light and sunlight transmittance of the polycarbonate substrates, and can perform the self-cleaning property.
  • Examples 1 to 8 show that the transparent substrate coated with the transparent aqua-based nano sol-gel of the present invention will not decrease the light transmittance and can perform the self-cleaning property.
  • Step 1 The transparent aqua-based nano sol-gel having the same formulation as in Example 2 was prepared.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of a polymethacrylate substrate having the thickness of 5 mm by the same coating method as in Example 2.
  • the surface of polymethacrylate substrate ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the polymethacrylate substrate ( 1 ), and a transparent coating film ( 2 ) was formed in a thickness of about 80-105 nm on the surface of the polymethacrylate substrate after cured with nature air drying for 24 hours.
  • a comparison of the transmittance at different wavelengths between the coated polymethacrylate substrate and uncoated polymethacrylate substrate is shown in FIG. 10 . It is obvious that the transmittance of the coated polymethacrylate substrate is higher than that of the uncoated polymethacrylate substrate.
  • Step 3 A comparison of the self-clean property between the coated polymethacrylate substrate and the uncoated polymethacrylate substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated and uncoated polymethacrylate substrates were firstly cleaned, and then the contact angle of a droplet on the two polymethacrylate substrates was measured, which was about 66°.
  • Oleic acid was evenly spread upon the surfaces of the coated and uncoated polymethacrylate substrates to simulate the contamination on the polymethacrylate substrate, and then the contact angle of a droplet was again measured, which was now about 73° indicating that the surfaces of the polymethacrylate substrates were contaminated by oleic acid.
  • the two contaminated polymethacrylate substrates were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated polymethacrylate substrates were measured at each period. The results are shown in Table 17.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated polymethacrylate substrate possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of polymethacrylate substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example.
  • the coated polymethacrylate substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3.
  • the results are shown in Table 18. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the polymethacrylate substrates will not decrease the visible light and sunlight transmittance of the polymethacrylate substrates, and can perform the self-cleaning property.
  • Step 1 The transparent aqua-based nano sol-gel having the same formulation as in Example 4 was prepared.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of a polystyrene substrate having the thickness of 5 mm by the same coating method as in Example 4.
  • the surface of polystyrene substrate ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the polystyrene substrate ( 1 ), and a transparent coating film ( 2 ) was formed in a thickness of about 43-67 nm on the surface of the polystyrene substrate after cured with nature air drying for 24 hours.
  • a comparison of the transmittance at different wavelengths between the coated polystyrene substrate and uncoated polystyrene substrate is shown in FIG. 11 . It is obvious that the transmittance of the coated polystyrene substrate is higher than that of the uncoated polystyrene substrate.
  • Step 3 A comparison of the self-clean property between the coated polystyrene substrate and the uncoated polystyrene substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated and uncoated polystyrene substrates were firstly cleaned, and then the contact angle of a droplet on the two polystyrene substrates was measured, which was about 68°.
  • Oleic acid was evenly spread upon the surfaces of the coated and uncoated polystyrene substrates to simulate the contamination on the polystyrene substrate, and then the contact angle of a droplet was again measured, which was now about 77° indicating that the surfaces of the polystyrene substrates were contaminated by oleic acid.
  • the two contaminated polystyrene substrates were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated polystyrene substrates were measured at each period. The results are shown in Table 19.
  • the lower contact angle indicates a better self-cleaning property.
  • the uncoated polystyrene substrate possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of polystyrene substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example.
  • the coated polystyrene substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3.
  • the results are shown in Table 20. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the polystyrene substrates will not decrease the visible light and sunlight transmittance of the polystyrene substrates, and can perform the self-cleaning property.
  • Step 1 The transparent aqua-based nano sol-gel having the same formulation as in Example 6 was prepared.
  • Step 2 The transparent aqua-based nano sol-gel was evenly applied to the surface of an epoxy substrate having the thickness of 5 mm by the same coating method as in Example 6. As shown in FIG. 1 , the surface of epoxy substrate ( 1 ) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the epoxy substrate ( 1 ), and a transparent coating film ( 2 ) was formed in a thickness of about 56-78 nm on the surface of the epoxy substrate after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated epoxy substrate and uncoated epoxy substrate is shown in FIG. 12 . It is obvious that the transmittance of the coated epoxy substrate is higher than that of the uncoated epoxy substrate.
  • Step 3 A comparison of the self-clean property between the coated epoxy substrate and the uncoated epoxy substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association.
  • the surfaces of both the coated and uncoated epoxy substrates were firstly cleaned, and then the contact angle of a droplet on the two epoxy substrates was measured, which was about 64°.
  • Oleic acid was evenly spread upon the surfaces of the coated and uncoated epoxy substrates to simulate the contamination on the epoxy substrate, and then the contact angle of a droplet was again measured, which was now about 76° indicating that the surfaces of the epoxy substrates were contaminated by oleic acid.
  • the two contaminated epoxy substrates were exposed to the irradiation of 1 mW/cm 2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated epoxy substrates were measured at each period. The results are shown in Table 21. The lower contact angle indicates a better self-cleaning property. Also, the uncoated epoxy substrate possesses no self-cleaning property at all.
  • the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • Step 4 The coating films having different thicknesses were formed on the surfaces of epoxy substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example.
  • the coated epoxy substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3.
  • the results are shown in Table 22. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the epoxy substrates will not decrease the visible light and sunlight transmittance of the epoxy substrates, and can perform the self-cleaning property.

Abstract

The present invention relates to a transparent aqua-based nano sol-gel composition and method of applying the same to transparent substrates without decreasing the visible light and sunlight transmittance thereof. The transparent aqua-based nano sol-gel can be applied to a surface of a transparent substrate to form a porous film which will not reduce the visible light and sunlight transmittance of the transparent substrate and will impart a self-cleaning function to the transparent substrate. The transparent aqua-based nano sol-gel composition contains a transparent aqua-based zeolite sol-gel having a particle size of less than 100 nm, a polysiloxane derivate, a surfactant, a transparent aqua-based photocatalytic sol-gel of titanium dioxide having a particle size of less than 100 nm, and deionized water.

Description

    CROSS REFERENCES TO RELATED APPLICATIONS
  • This application is a divisional of U.S. Ser. No. 12/267,025 filed Nov. 7, 2008, which claims priority to Taiwan Patent Application No. 96142648, filed Nov. 12, 2007, entitled “TRANSPARENT AQUA-BASED NANO SOL-GEL COMPOSITION AND METHOD OF APPLYING THE SAME” which is expressly incorporated by reference herein, in its entirety.
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention as disclosed herein and further defined by the claims relates to a transparent aqua-based nano sol-gel composition and a method of applying the same to transparent substrates without decreasing the visible light and sunlight transmittance thereof. The transparent aqua-based nano sol-gel can be applied to a surface of a transparent substrate to form a porous film which will not reduce the visible light and sunlight transmittance of the transparent substrate and will impart a self-cleaning function to the transparent substrate. The transparent aqua-based nano sol-gel composition comprises a transparent aqua-based zeolite sol-gel having a particle size of less than 100 nm, a polysiloxane derivate, a surfactant, a transparent aqua-based photocatalytic sol-gel of titanium dioxide having a particle size of less than 100 nm, and deionized water.
  • 2. Description of the Related Art
  • Transparent substrates are always used as protection covers of solar energy products and lighting lamps, and the transmittance of the transparent substrates to lights plays an important role to the total efficiency of these products. Generally, glass is used as the transparent substrate, and the reflectivity of glass substrate to light is about 8%. If the reflectivity of glass substrate can be reduced, the transmittance of glass substrate can be increased. In addition, the contaminants or stains on the glass substrates will remarkably reduce the transmittance to light, hence it is desirable to impart the self-cleaning function to the glass substrates and to increase the transmittance of glass substrate to light.
  • In the market, the anti-reflective glass capable of increasing the transmittance to light and the photocatalyst-coated glass with self-cleaning function have been put into mass production. However, the photocatalyst-coated glass is generally coated with titanium dioxide (TiO2) having high refractive index, and the visible light and sunlight reflectivity thereof is about 12% and hence the transmittance thereof is reduced. Moreover, the application of coating film to the glass is mostly conducted by processes such as vacuum sputtering, physical vapor deposition, chemical vapor deposition, etc. using low pressure vacuum equipment which is very expensive. Despite its innovation and advantage, the functional glass is too expensive to be accepted by the general consuming public. It is therefore important to develop the functional glass with low cost.
  • U.S. Pat. No. 5,216,542 discloses a multilayer coating structure upon transparent substrate. The top layer of the multilayer structure is silicon dioxide (SiO2) and has a refractive index of 1.46 at a wavelength of 550 nm, which has anti-reflection effect but no self-cleaning property.
  • U.S. Pat. No. 5,105,310 discloses a multilayer anti-reflection coating upon transparent substrate. The top layer of the multilayer structure is silicon dioxide (SiO2) and has a refractive index of 1.46 at a wavelength of 550 nm, which has anti-reflection effect but no self-cleaning property.
  • U.S. Pat. No. 5,147,125 discloses a multilayer anti-reflection coating upon transparent substrate. The top layer of the multilayer structure is Magnesium Fluoride (MgF2) and has a refractive index of 1.38 at a wavelength of 550 nm, which has anti-reflection effect but no self-cleaning property.
  • China Patent No. CN1447133A discloses an anti-reflection layer which is transparent, conductive and can increase the transmittance to light. The top layer of the multilayer is an ITO layer (Indium Tin Oxide), which has anti-reflection effect but no self-cleaning property.
  • China Patent No. CN1101353C discloses self-cleaning glass and its manufacturing method. The titanium dioxide layer is deposited on the surface of glass by a sputtering process which is expensive. The coated glass has self-cleaning property and its refractive index is about 2.5˜2.7. However, the coated glass with high refractive index will remarkably reduce the transmittance to light.
  • China Patent No. CN1579981A discloses photocatalyst-coated glass and its manufacturing method. The titanium dioxide layer is deposited on the surface of glass by a vacuum sputtering process which is expensive. The coated glass has self-cleaning property and its refractive index is about 2.5˜2.7. However, the coated glass with high refractive index will remarkably reduce the transmittance to light.
  • China Patent No. CN1660955A discloses a spray agent for nano photocatalyst-coated glass and its preparation method. The nano photocatalyst liquid consists of titanium dioxide nanopowder and other nanopowder dispensed in the dispersants. The nano photocatalyst liquid is turbid and will reduce the transmittance to light after coated on the glass.
  • Taiwan Patent No. 00313630 discloses a method of photocatalytically making the surface of a base material ultrahydrophilic, a base material having ultrahydrophilic and photocatalytic surface, and a process for producing said material. This invention only describes the applications of photocatalyst to different substrates; however, no discussion is made regarding the optical performance for the coated substrates. In addition, parts of the method/process of this invention require the use of 900° C. and such a high temperature is not convenient for all types of substrates.
  • At present time, there is no commercially available transparent substrate which will not reduce the transmittance to light and possess the self-cleaning property. Therefore, it is the main objective of the present invention to develop a method of manufacturing transparent substrates which will not reduce the visible light and sunlight transmittance and possess the self-cleaning property at low production cost.
  • BRIEF SUMMARY
  • The main objective of the present invention is to provide a transparent aqua-based nano sol-gel composition applying to transparent substrates without decreasing the visible light and sunlight transmittance thereof. The transparent aqua-based nano sol-gel can be applied to a surface of a transparent substrate to form a porous film which will not reduce the visible light and sunlight transmittance of the transparent substrate and will impart a self-cleaning function to the transparent substrate. The transparent aqua-based nano sol-gel composition comprises a transparent aqua-based zeolite sol-gel having a particle size of less than 100 nm, a polysiloxane derivate, a surfactant, a transparent aqua-based photocatalytic sol-gel of titanium dioxide having a particle size of less than 100 nm, and deionized water. The test method for the self-cleaning property refers to “Test Method for Self-Cleaning Performance of Photocatalytic Building Materials” published by the Taiwan Photocatalyst Industry Association. The process of the test method comprises the steps of applying the oleic acid to the photocatalytic substrate and making the contact angle of droplet on the substrate higher than 30°. After exposing the substrate under the UVA light with intensity of 1 mW/cm2 or above for 24 hours, the oleic acid applied to the photocatalytic surface can be decomposed and the contact angle of droplet on the substrate is less than 15°.
  • The present invention can reduce the high production costs of the conventional art, simplify the production process, lower the production temperature, save energy, lower the production cost, and is environmental friendly.
  • The present invention relates to a transparent aqua-based nano sol-gel composition and a method of applying the same to transparent substrates without decreasing the visible light and sunlight transmittance thereof. The method of applying the transparent aqua-based nano sol-gel composition to transparent substrates comprises the steps of:
  • 1. preparing the transparent aqua-based sol-gel: a transparent aqua-based zeolite sol-gel having a particle size of less than 100 nm, a polysiloxane derivate, a surfactant, a transparent aqua-based photocatalytic sol-gel of titanium dioxide having a particle size of less than 100 nm, and deionized water are well mixed and filtered to obtain the transparent aqua-based sol-gel.
  • 2. preparing the coating film upon transparent substrates: the transparent aqua-based nano sol-gel is applied to a surface of a transparent substrate evenly to form a transparent coating film and then the coating film is cured by a predetermined curing process so that the transparent coating film can adhere to the surface of the substrate more rigidly and reliably. The dry film thickness of the finished transparent aqua-based coating film is between 40˜350 nm.
  • The transparent aqua-based nano sol-gel composition according to the present invention is characterized by comprising: a transparent aqua-based zeolite sol-gel in a solid content of 0.1˜15.0 wt %, preferably 0.1˜10 wt %, and more preferably 0.1˜5 wt %; a polysiloxane derivate in a solid content of 0.0001˜10.0 wt %, preferably 0.001˜17 wt %, and more preferably 0.01˜3 wt %, wherein the polysiloxane derivate is selected from the group consisting of methyltrimethoxysilane, methyltriethoxysilane, ethyltributoxysilane, trimethyldiethyoxysilane, dimethoxymethylphenylsilane, triethoxypropylsilane, tripropoxypropylsilane and tributoxymethylsilane; a non-ionic surfactant in a solid content of 0.0001˜10.0 wt %, preferably 0.001˜5 wt %, and more preferably 0.01˜3 wt %, wherein the surfactant is selected from the group consisting of polyoxyethylene p-octylphenol ether, polyoxyethylene p-octyl laurate, polyoxyethylene sorbitol laurate, polyoxyethylene oleoyl ether, polyoxyethylene stearyl ether, polyoxyethylene sorbitan laurate and oleic diethanol amide; a transparent aqua-based photocatalytic sol-gel of titanium dioxide in a solid content of 0.1˜2.0 wt %, preferably 0.1˜1.5 wt %, and more preferably 0.1˜1 wt %.
  • The transparent aqua-based nano sol-gel composition is evenly applied to the surface of the transparent substrate with any wet coating method selected from a roll coating method, a wipe coating method, a brush coating method, a dip coating method, a spray coating method, a spin coating method or a sprinkle coating method, which can be carried out to coat one side or both sides of the transparent substrate. The “coating film is cured by a predetermined curing process” mentioned above refers to curing the coating film with natural air drying for 24 hours or above, or heating at a temperature of 450° C. or below for 5 minutes or above.
  • The transparent substrate referred to in the present invention can be selected from the group consisting of glass and plastic substrates, including transparent glass, transparent polycarbonate resins, transparent polymethacrylate resins, transparent polystyrene resins and transparent epoxy resins.
  • The transparent coating film formed upon transparent substrates according to the present invention possesses self-cleaning property under light irradiation, and the light can be either sun light or artificial light.
  • BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
  • FIG. 1 shows the transparent substrate and the coating film according to the present invention.
  • FIG. 2 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 1.
  • FIG. 3 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 2.
  • FIG. 4 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 3.
  • FIG. 5 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 4.
  • FIG. 6 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 5.
  • FIG. 7 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 6.
  • FIG. 8 shows the light transmittance comparison for extra-white glass before coating and after coating according to Example 7.
  • FIG. 9 shows the light transmittance comparison for transparent polycarbonate resins substrate before coating and after coating according to Example 8.
  • FIG. 10 shows the light transmittance comparison for transparent polymethacrylate resins substrate before coating and after coating according to Example 9.
  • FIG. 11 shows the light transmittance comparison for transparent polystyrene resins substrate before coating and after coating according to Example 10.
  • FIG. 12 shows the light transmittance comparison for transparent epoxy resins substrate before coating and after coating according to Example 11.
  • DETAILED DESCRIPTION
  • For the purposes of promoting an understanding of the disclosure, reference will now be made to the embodiments illustrated in the drawings and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the disclosure is thereby intended, such alterations and further modifications in the illustrated device and its use, and such further applications of the principles of the disclosure as illustrated therein being contemplated as would normally occur to one skilled in the art to which the disclosure relates.
  • To operationally verify the preparation of the transparent aqua-based nano sol-gel composition and method of applying the same in accordance with the present invention, eleven examples are illustrated as follows.
  • Further benefits and advantages of the present invention will become apparent after a careful reading of the detailed description.
  • Example 1
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 0.1 wt % solid content of a transparent aqua-based zeolite sol-gel, 0.0001 wt % solid content of methyltrimethoxysilane as the polysiloxane derivate, 0.0001 wt % solid content of polyoxyethylene p-octylphenol ether as the non-ionic surfactant, 0.1 wt % solid content of the transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a dip coating method. As shown in FIG. 1, the surface of glass (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass (1) by a dip coating method, and a transparent coating film (2) was formed in a thickness of about 40-50 nm on the surface of the glass after cured with nature air drying for 24 hours. A comparison of the transmittance (T %) at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 2. It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3: A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°. Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 67° indicating that the surfaces of the pieces of glass were contaminated by oleic acid. The two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period. The results are shown in Table 1. The lower contact angle indicates a better self-cleaning property. Also, the uncoated glass possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 1
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated glass Coated glass
    0 hours 67° 67° 
    24 hours 67°
    48 hours 67°
    72 hours 67°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 2. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • TABLE 2
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    coated glass with
    Thickness of Curing Comparison of light oleic acid
    Item coating film condition transmittance contamination
    1 100-120 nm  90° C. The light transmittance of the 0 hours 66° 
    360 min.  coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
    2 250-272 nm 200° C. The light transmittance of the 0 hours 66° 
    60 min. coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
    3 330-344 nm 450° C. The light transmittance of the 0 hours 66° 
     5 min. coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
  • Example 2
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 15.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 10 wt % solid content of methyltriethoxysilane as the polysiloxane derivate, 10 wt % solid content of polyoxyethylene p-octyl laurate as the non-ionic surfactant, 2 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a spin coating method. As shown in FIG. 1, the surface of glass (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass (1) by a spin coating method, and a transparent coating film (2) was formed in a thickness of about 120-132 nm on the surface of the glass after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 3. It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3: A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°. Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 65° indicating that the surfaces of the pieces of glass were contaminated by oleic acid. The two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period. The results are shown in Table 3. The lower contact angle indicates a better self-cleaning property. Also, the uncoated glass possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 3
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated glass Coated glass
    0 hours 65° 65° 
    24 hours 65°
    48 hours 65°
    72 hours 65°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 4. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • TABLE 4
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    Thickness coated glass
    of coating Curing Comparison of light with oleic acid
    Item film condition transmittance contamination
    1 325-335 nm 150° C. The light transmittance of the 0 hours 65° 
    240 min.  coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
    2 160-180 nm 350° C. The light transmittance of the 0 hours 65° 
    40 min. coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
    3 260-278 nm 450° C. The light transmittance of the 0 hours 65° 
    10 min. coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
  • Example 3
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 2.0 wt % solid content of transparent aqua-based zeolite sol-gel, 3.0 wt % solid content of ethyltributoxysilane as the polysiloxane derivate, 2.0 wt % solid content of polyoxyethylene sorbitol laurate as the non-ionic surfactant, 0.7 wt % solid content of transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a wipe coating method. As shown in FIG. 1, the surface of glass (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass (1) by a wipe coating method, and a transparent coating film (2) was formed in a thickness of about 95-105 nm on the surface of the glass after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 4. It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3: A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°. Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 68° indicating that the surfaces of the pieces of glass were contaminated by oleic acid. The two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period. The results are shown in Table 5. The lower contact angle indicates a better self-cleaning property. Also, the uncoated glass possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 5
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated glass Coated glass
    0 hours 68° 68° 
    24 hours 68°
    48 hours 68°
    72 hours 68°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 6. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • TABLE 6
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    Thickness coated glass with
    of coating Curing Comparison of light oleic acid
    Item film condition transmittance contamination
    1 58-70 nm 120° C. The light transmittance of the 0 hours 68° 
    300 min.  coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
    2 335-350 nm 320° C. The light transmittance of the 0 hours 68° 
    60 min. coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
    3 202-215 nm 450° C. The light transmittance of the 0 hours 68° 
     5 min. coated glass is higher than 24 hours
    that of uncoated glass. 48 hours
    72 hours
  • Example 4
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 5.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 6.0 wt % solid content of trimethyldiethyoxysilane as the polysiloxane derivate, 8.0 wt % solid content of polyoxyethylene oleoyl ether as the non-ionic surfactant, 1.0 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a roll coating method. As shown in FIG. 1, the surface of glass (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass (1) by a roll coating method, and a transparent coating film (2) was formed in a thickness of about 125-146 nm on the surface of the glass after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 5. It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3: A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°. Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 64° indicating that the surfaces of the pieces of glass were contaminated by oleic acid. The two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period. The results are shown in Table 7. The lower contact angle indicates a better self-cleaning property. Also, the uncoated glass possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 7
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated glass Coated glass
    0 hours 64° 64° 
    24 hours 64°
    48 hours 64°
    72 hours 64°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 8. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • TABLE 8
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    Thickness coated glass with
    of coating Curing Comparison of light oleic acid
    Item film condition transmittance contamination
    1 82-95 nm  80° C. The light transmittance of 0 hours 64° 
    480 min.  the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
    2 295-320 nm 280° C. The light transmittance of 0 hours 64° 
    70 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
    3 222-246 nm 420° C. The light transmittance of 0 hours 64° 
    10 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
  • Example 5
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 10.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 10.0 wt % solid content of dimethoxymethylsilane as the polysiloxane derivate, 2.0 wt % solid content of polyoxyethylene stearyl ether as the non-ionic surfactant, 1.5 wt % solid content of transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a spray coating method. As shown in FIG. 1, the surface of glass (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass (1) by a spray coating method, and a transparent coating film (2) was formed in a thickness of about 140-170 nm on the surface of the glass after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 6. It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3: A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°. Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 69° indicating that the surfaces of the pieces of glass were contaminated by oleic acid. The two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period. The results are shown in Table 9. The lower contact angle indicates a better self-cleaning property. Also, the uncoated glass possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 9
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated glass Coated glass
    0 hours 69° 69° 
    24 hours 69°
    48 hours 69°
    72 hours 69°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 10. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • TABLE 10
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    coated glass with
    Thickness of Curing Comparison of light oleic acid
    Item coating film condition transmittance contamination
    1 95-120 nm 150° C. The light transmittance of 0 hours 69° 
    180 min.  the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
    2 198-220 nm 300° C. The light transmittance of 0 hours 69° 
    60 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
    3 328-350 nm 400° C. The light transmittance of 0 hours 69° 
    10 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
  • Example 6
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 7.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 1.0 wt % solid content of methyltributoxysilane as the polysiloxane derivate, 5.0 wt % solid content of oleic diethanol amide as the non-ionic surfactant, 0.8 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a brush coating method. As shown in FIG. 1, the surface of glass (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass (1) by a brush coating method, and a transparent coating film (2) was formed in a thickness of about 136-164 nm on the surface of the glass after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 7. It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3: A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°. Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 66° indicating that the surfaces of the pieces of glass were contaminated by oleic acid. The two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period. The results are shown in Table 11. The lower contact angle indicates a better self-cleaning property. Also, the uncoated glass possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 11
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated glass Coated glass
    0 hours 66° 66° 
    24 hours 66°
    48 hours 66°
    72 hours 66°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 12. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • TABLE 12
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    coated glass with
    Thickness of Curing Comparison of light oleic acid
    Item coating film condition transmittance contamination
    1 43-58 nm 200° C. The light transmittance of 0 hours 66° 
    120 min.  the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
    2 256-283 nm 300° C. The light transmittance of 0 hours 66° 
    60 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
    3 312-350 nm 450° C. The light transmittance of 0 hours 66° 
    10 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
  • Example 7
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 3.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 3.0 wt % solid content of propyltripropoxysilane as the polysiloxane derivate, 2.0 wt % solid content of polyoxyethylene sorbitan laurate as the non-ionic surfactant, 0.6 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of the extra-white glass having the thickness of 5 mm by a sprinkle coating method. As shown in FIG. 1, the surface of glass (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the glass (1) by a sprinkle coating method, and a transparent coating film (2) was formed in a thickness of about 65-80 nm on the surface of the glass after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated extra-white glass and uncoated extra-white glass is shown in FIG. 8. It is obvious that the transmittance of the coated glass is higher than that of the uncoated glass.
  • Step 3: A comparison of the self-clean property between the coated glass and the uncoated glass was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated glass and uncoated glass were firstly cleaned, and then the contact angle of a droplet on the two pieces of glass was measured, which was about 35°. Oleic acid was evenly spread upon the surfaces of the coated glass and the uncoated glass to simulate the contamination on the glass, and then the contact angle of a droplet was again measured, which was now about 64° indicating that the surfaces of the pieces of glass were contaminated by oleic acid. The two pieces of contaminated glass were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two pieces of contaminated glass were measured at each period. The results are shown in Table 13. The lower contact angle indicates a better self-cleaning property. Also, the uncoated glass possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 13
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated glass Coated glass
    0 hours 64° 64°
    24 hours 64° 10°
    48 hours 64°  8°
    72 hours 64°  7°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of glass substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The pieces of coated glass were then cured under different conditions, and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 14. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the glass will not decrease the visible light and sunlight transmittance of the glass, and can perform the self-cleaning property.
  • TABLE 14
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    coated glass with
    Thickness of Curing Comparison of light oleic acid
    Item coating film condition transmittance contamination
    1 120-142 nm 150° C. The light transmittance of 0 hours 64° 
    240 min.  the coated glass is higher 24 hours 10° 
    than that of uncoated glass. 48 hours
    72 hours
    2 263-285 nm 300° C. The light transmittance of 0 hours 64° 
    60 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
    3 320-345 nm 450° C. The light transmittance of 0 hours 64° 
    10 min. the coated glass is higher 24 hours
    than that of uncoated glass. 48 hours
    72 hours
  • Example 8
  • Step 1: A transparent aqua-based nano sol-gel was prepared and obtained by well mixing and then filtering the materials comprising 12.0 wt % solid content of a transparent aqua-based zeolite sol-gel, 0.1 wt % solid content of propyltriethoxysilane as the polysiloxane derivate, 0.1 wt % solid content of polyoxyethylene p-octyl laurate as the non-ionic surfactant, 1.8 wt % solid content of a transparent aqua-based photocatalytic sol-gel of titanium dioxide, and the rest of de-ionized water.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of a polycarbonate substrate having the thickness of 5 mm by a brush coating method. As shown in FIG. 1, the surface of the polycarbonate substrate was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the polycarbonate substrate (1) by a brush coating method, and a transparent coating film (2) was formed in a thickness of about 40-60 nm on the surface of the polycarbonate substrate after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated polycarbonate substrate and uncoated polycarbonate substrate is shown in FIG. 9. It is obvious that the transmittance of the coated polycarbonate substrate is higher than that of the uncoated polycarbonate substrate.
  • Step 3: A comparison of the self-clean property between the coated polycarbonate substrate and the uncoated polycarbonate substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated and uncoated polycarbonate substrates were firstly cleaned, and then the contact angle of a droplet on the two polycarbonate substrates was measured, which was about 65°. Oleic acid was evenly spread upon the surfaces of the coated and uncoated polycarbonate substrates to simulate the contamination on the polycarbonate substrate, and then the contact angle of a droplet was again measured, which was now about 75° indicating that the surfaces of the polycarbonate substrates were contaminated by oleic acid. The two contaminated polycarbonate substrates were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated polycarbonate substrates were measured at each period. The results are shown in Table 15. The lower contact angle indicates a better self-cleaning property. Also, the uncoated polycarbonate substrate possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 15
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated transparent Coated transparent
    polycarbonate polycarbonate
    substrate substrate
    0 hours 75° 75°
    24 hours 75° 15°
    48 hours 75° 11°
    72 hours 75° 10°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of polycarbonate substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The coated polycarbonate substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 16. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the polycarbonate substrates will not decrease the visible light and sunlight transmittance of the polycarbonate substrates, and can perform the self-cleaning property.
  • TABLE 16
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    Thickness coated polycarbonate
    of coating Curing Comparison of light substrates with oleic
    Item film condition transmittance acid contamination
    1 375-395 nm 80° C. The light transmittance of 0 hours 75°
    120 min. the coated polycarbonate 24 hours 17°
    substrate is higher than that 48 hours 12°
    of uncoated polycarbonate 72 hours  8°
    substrate.
    2 130-165 nm 80° C. The light transmittance of 0 hours 75°
    120 min. the coated polycarbonate 24 hours 18°
    substrate is higher than that 48 hours 14°
    of uncoated polycarbonate 72 hours  9°
    substrate.
    3 240-268 nm 80° C. The light transmittance of 0 hours 75°
    120 min. the coated polycarbonate 24 hours 16°
    substrate is higher than that 48 hours 11°
    of uncoated polycarbonate 72 hours  8°
    substrate.
  • The results of Examples 1 to 8 show that the transparent substrate coated with the transparent aqua-based nano sol-gel of the present invention will not decrease the light transmittance and can perform the self-cleaning property.
  • Example 9
  • Step 1: The transparent aqua-based nano sol-gel having the same formulation as in Example 2 was prepared.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of a polymethacrylate substrate having the thickness of 5 mm by the same coating method as in Example 2. As shown in FIG. 1, the surface of polymethacrylate substrate (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the polymethacrylate substrate (1), and a transparent coating film (2) was formed in a thickness of about 80-105 nm on the surface of the polymethacrylate substrate after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated polymethacrylate substrate and uncoated polymethacrylate substrate is shown in FIG. 10. It is obvious that the transmittance of the coated polymethacrylate substrate is higher than that of the uncoated polymethacrylate substrate.
  • Step 3: A comparison of the self-clean property between the coated polymethacrylate substrate and the uncoated polymethacrylate substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated and uncoated polymethacrylate substrates were firstly cleaned, and then the contact angle of a droplet on the two polymethacrylate substrates was measured, which was about 66°. Oleic acid was evenly spread upon the surfaces of the coated and uncoated polymethacrylate substrates to simulate the contamination on the polymethacrylate substrate, and then the contact angle of a droplet was again measured, which was now about 73° indicating that the surfaces of the polymethacrylate substrates were contaminated by oleic acid. The two contaminated polymethacrylate substrates were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated polymethacrylate substrates were measured at each period. The results are shown in Table 17. The lower contact angle indicates a better self-cleaning property. Also, the uncoated polymethacrylate substrate possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 17
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated transparent Coated transparent
    polymethacrylate polymethacrylate
    substrate substrate
    0 hours 73° 73°
    24 hours 73° 18°
    48 hours 73° 14°
    72 hours 73°  9°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of polymethacrylate substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The coated polymethacrylate substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 18. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the polymethacrylate substrates will not decrease the visible light and sunlight transmittance of the polymethacrylate substrates, and can perform the self-cleaning property.
  • TABLE 18
    Variations in light transmittance and contact angle under different process conditions
    Contact angle on
    coated polymethacrylate
    Thickness of Curing Comparison of light substrates with oleic
    Item coating film condition transmittance acid contamination
    1 315-335 nm 80° C. The light transmittance of the 0 hours 73°
    120 min. coated polymethacrylate 24 hours 19°
    substrate is higher than that of 48 hours 15°
    uncoated polymethacrylate 72 hours  8°
    substrate.
    2 140-175 nm 80° C. The light transmittance of the 0 hours 73°
    120 min. coated polymethacrylate 24 hours 18°
    substrate is higher than that of 48 hours 14°
    uncoated polymethacrylate 72 hours 11°
    substrate.
    3 250-278 nm 80° C. The light transmittance of the 0 hours 73°
    120 min. coated polymethacrylate 24 hours 19°
    substrate is higher than that of 48 hours 16°
    uncoated polymethacrylate 72 hours 13°
    substrate.
  • Example 10
  • Step 1: The transparent aqua-based nano sol-gel having the same formulation as in Example 4 was prepared.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of a polystyrene substrate having the thickness of 5 mm by the same coating method as in Example 4. As shown in FIG. 1, the surface of polystyrene substrate (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the polystyrene substrate (1), and a transparent coating film (2) was formed in a thickness of about 43-67 nm on the surface of the polystyrene substrate after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated polystyrene substrate and uncoated polystyrene substrate is shown in FIG. 11. It is obvious that the transmittance of the coated polystyrene substrate is higher than that of the uncoated polystyrene substrate.
  • Step 3: A comparison of the self-clean property between the coated polystyrene substrate and the uncoated polystyrene substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated and uncoated polystyrene substrates were firstly cleaned, and then the contact angle of a droplet on the two polystyrene substrates was measured, which was about 68°. Oleic acid was evenly spread upon the surfaces of the coated and uncoated polystyrene substrates to simulate the contamination on the polystyrene substrate, and then the contact angle of a droplet was again measured, which was now about 77° indicating that the surfaces of the polystyrene substrates were contaminated by oleic acid. The two contaminated polystyrene substrates were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated polystyrene substrates were measured at each period. The results are shown in Table 19. The lower contact angle indicates a better self-cleaning property. Also, the uncoated polystyrene substrate possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 19
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated transparent Coated transparent
    polystyrene polystyrene
    substrate substrate
    0 hours 77° 77°
    24 hours 77° 22°
    48 hours 77° 18°
    72 hours 77° 11°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of polystyrene substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The coated polystyrene substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 20. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the polystyrene substrates will not decrease the visible light and sunlight transmittance of the polystyrene substrates, and can perform the self-cleaning property.
  • TABLE 20
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    coated polystyrene
    Thickness of Curing Comparison of light substrates with oleic
    Item coating film condition transmittance acid contamination
    1 315-335 nm 80° C. The light transmittance of the 0 hours 73°
    120 min. coated polystyrene substrate 24 hours 19°
    is higher than that of 48 hours 15°
    uncoated polystyrene substrate. 72 hours  8°
    2 140-175 nm 80° C. The light transmittance of the 0 hours 73°
    120 min. coated polystyrene substrate 24 hours 18°
    is higher than that of 48 hours 14°
    uncoated polystyrene substrate. 72 hours 11°
    3 250-278 nm 80° C. The light transmittance of the 0 hours 73°
    120 min. coated polystyrene substrate 24 hours 19°
    is higher than that of 48 hours 16°
    uncoated polystyrene substrate. 72 hours 13°
  • Example 11
  • Step 1: The transparent aqua-based nano sol-gel having the same formulation as in Example 6 was prepared.
  • Step 2: The transparent aqua-based nano sol-gel was evenly applied to the surface of an epoxy substrate having the thickness of 5 mm by the same coating method as in Example 6. As shown in FIG. 1, the surface of epoxy substrate (1) was firstly cleaned, then the transparent aqua-based nano sol-gel was evenly applied to the surface of the epoxy substrate (1), and a transparent coating film (2) was formed in a thickness of about 56-78 nm on the surface of the epoxy substrate after cured with nature air drying for 24 hours. A comparison of the transmittance at different wavelengths between the coated epoxy substrate and uncoated epoxy substrate is shown in FIG. 12. It is obvious that the transmittance of the coated epoxy substrate is higher than that of the uncoated epoxy substrate.
  • Step 3: A comparison of the self-clean property between the coated epoxy substrate and the uncoated epoxy substrate was carried out by using the method of “Test Method for Self-Cleaning performance of Photocatalytic Building Materials” published by Taiwan Photocatalyst Industry Association. The surfaces of both the coated and uncoated epoxy substrates were firstly cleaned, and then the contact angle of a droplet on the two epoxy substrates was measured, which was about 64°. Oleic acid was evenly spread upon the surfaces of the coated and uncoated epoxy substrates to simulate the contamination on the epoxy substrate, and then the contact angle of a droplet was again measured, which was now about 76° indicating that the surfaces of the epoxy substrates were contaminated by oleic acid. The two contaminated epoxy substrates were exposed to the irradiation of 1 mW/cm2 of UVA light for 24 hours, 48 hours and 72 hours, and the transmittance and contact angle of the two contaminated epoxy substrates were measured at each period. The results are shown in Table 21. The lower contact angle indicates a better self-cleaning property. Also, the uncoated epoxy substrate possesses no self-cleaning property at all.
  • As a conclusion from the above Step 2 and Step 3, the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the transparent substrates will not decrease the visible light and sunlight transmittance of the transparent substrates, and can perform the self-cleaning property.
  • TABLE 21
    Variation in contact angle of oleic acid contaminated
    surface under different UVA exposure periods
    Uncoated transparent Coated transparent
    epoxy substrate epoxy substrate
    0 hours 76° 76°
    24 hours 76° 17°
    48 hours 76° 13°
    72 hours 76° 11°
  • Step 4: The coating films having different thicknesses were formed on the surfaces of epoxy substrates having the thickness of 5 mm with the same formulation of transparent aqua-based nano sol-gel and coating method as this example. The coated epoxy substrates were then cured under different conditions at a temperature of lower than 100° C., and the self-cleaning property and transmittance thereof were measured by following the above Step 2 and Step 3. The results are shown in Table 22. It is clear that the film formed by applying the transparent aqua-based nano sol-gel of the present invention to the epoxy substrates will not decrease the visible light and sunlight transmittance of the epoxy substrates, and can perform the self-cleaning property.
  • TABLE 22
    Variations in light transmittance and contact
    angle under different process conditions
    Contact angle on
    Thickness coated epoxy
    of coating Curing Comparison of light substrates with oleic
    Item film condition transmittance acid contamination
    1 315-335 nm 80° C. The light transmittance of the 0 hours 76°
    120 min coated epoxy substrate 24 hours 20°
    is higher than that of 48 hours 15°
    uncoated epoxy substrate. 72 hours 12°
    2 140-175 nm 80° C. The light transmittance of the 0 hours 76°
    120 min coated epoxy substrate 24 hours 18°
    is higher than that of 48 hours 14°
    uncoated epoxy substrate. 72 hours 10°
    3 250-278 nm 80° C. The light transmittance of the 0 hours 76°
    120 min coated epoxy substrate 24 hours 18°
    is higher than that of 48 hours 13°
    uncoated epoxy substrate. 72 hours 11°
  • Although the present invention has been explained in relation to multiple preferred embodiments in these examples, many other possible modifications and variations can be made without departing from the spirit and scope of the present invention as hereinafter claimed.
  • While the preferred embodiment of the invention has been illustrated and described in the drawings and foregoing description, the same is to be considered as illustrative and not restrictive in character, it being understood that all changes and modifications that come within the spirit of the invention are desired to be protected.

Claims (7)

1. A method of applying a transparent aqua-based nano sol-gel composition, comprising:
(i) the step of preparing a transparent aqua-based nano sol-gel by well mixing, and then filtering, the transparent aqua-based nano sol-gel composition as claimed in claim 1 to obtain a transparent aqua-based nano sol-gel; and
(ii) the step of preparing a coating film upon a transparent substrate by applying the transparent aqua-based nano sol-gel to a surface of the transparent substrate evenly to form a transparent coating film and then curing the coating film while retaining the evenness of the coating film so that the transparent coating film can adhere to the surface of the substrate more rigidly and reliably.
2. The method of applying a transparent aqua-based nano sol-gel composition as claimed in claim 1, wherein in step (ii), the transparent aqua-based nano sol-gel is evenly applied to the surface of the transparent substrate with any wet coating method selected from a roll coating method, a wipe coating method, a brush coating method, a dip coating method, a spray coating method, a spin coating method and a sprinkle coating method.
3. The method of applying a transparent aqua-based nano sol-gel composition as claimed in claim 1, which can be carried out to coat one side or both sides of the substrate.
4. The method of applying a transparent aqua-based nano sol-gel composition as claimed in claim 2, which can be carried out to coat one side or both sides of the substrate.
5. The method of applying a transparent aqua-based nano sol-gel composition as claimed in claim 1, wherein in step (ii), the coating film is cured with natural air drying for 24 hours or above, or heating at a temperature of 450° C. or below for 5 minutes or above.
6. The method of applying a transparent aqua-based nano sol-gel composition as claimed in claim 1, wherein the dry film thickness of the finished transparent aqua-based coating film is between 40˜350 nm.
7. The method of applying a transparent aqua-based nano sol-gel composition as claimed in claim 5, wherein the dry film thickness of the finished transparent aqua-based coating film is between 40˜350 nm.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103042770A (en) * 2012-09-14 2013-04-17 泉耀新材料科技(苏州)有限公司 Building material glass of Titanium dioxide coating film with porosity structure and low refractive index
US10543061B2 (en) 2014-10-03 2020-01-28 3M Innovative Properties Company Methods for managing the scattering of incident light and articles created therefrom

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8367756B2 (en) * 2007-12-27 2013-02-05 Eastman Kodak Company Stabilized coating dispersions for porous inkjet recording media
JP5570538B2 (en) * 2012-01-17 2014-08-13 株式会社都ローラー工業 Functional coating agent coating method and coating apparatus for substrate
CN102997126A (en) * 2012-08-22 2013-03-27 苏州金科信汇光电科技有限公司 Wall washer lamp with self-cleaning function
FR3004130B1 (en) * 2013-04-08 2015-12-11 Ecole Norm Superieure Lyon METHOD FOR DEPOSITING A PHOTOCATALYTIC COATING, COATINGS, TEXTILE MATERIALS AND USE IN PHOTOCATALYSIS
JP6487708B2 (en) * 2014-02-24 2019-03-20 Toto株式会社 Coating composition and painted body
CN104801290B (en) * 2015-04-01 2017-07-18 盐城工学院 The preparation method of A compound-eye-type titanium dioxide/mesoporous carbon composite visible light catalytic material
CN113416479A (en) * 2021-06-24 2021-09-21 湖南省金海科技有限公司 Development and preparation method of two-component water-based sprinkling paint
CN113529095A (en) * 2021-08-05 2021-10-22 漳州市兴达辉机械有限公司 Surface treatment process for handle connecting cross rod

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6020419A (en) * 1998-03-18 2000-02-01 Bayer Aktiengesellschaft Transparent coating compositions containing nanoscale particles and having improved scratch resistance
US20020045010A1 (en) * 2000-06-14 2002-04-18 The Procter & Gamble Company Coating compositions for modifying hard surfaces
US6680135B2 (en) * 1995-09-15 2004-01-20 Saint-Gobain Glass France Substrate with a photocatalytic coating

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5147125A (en) 1989-08-24 1992-09-15 Viratec Thin Films, Inc. Multilayer anti-reflection coating using zinc oxide to provide ultraviolet blocking
DE3941797A1 (en) 1989-12-19 1991-06-20 Leybold Ag BELAG, CONSISTING OF AN OPTICAL LAYER SYSTEM, FOR SUBSTRATES, IN WHICH THE LAYER SYSTEM IN PARTICULAR HAS A HIGH ANTI-FLEXIBLE EFFECT, AND METHOD FOR PRODUCING THE LAMINATE
US5105310A (en) 1990-10-11 1992-04-14 Viratec Thin Films, Inc. Dc reactively sputtered antireflection coatings
JP2636692B2 (en) * 1993-08-06 1997-07-30 レジノカラー工業株式会社 Rush treatment agent
TW313630B (en) 1996-03-21 1997-08-21 Toto Ltd The surface substrate with light catalyst and hydrophilicity and its manufacturing method
JP3976851B2 (en) * 1996-09-13 2007-09-19 古河機械金属株式会社 Method for producing titanium dioxide fine particles, method for producing photocatalyst powder for NOX purification, method for producing paint, method for producing building material
JPH10196229A (en) * 1997-01-16 1998-07-28 Dainippon Printing Co Ltd Window
JP3260097B2 (en) * 1997-05-16 2002-02-25 大日本塗料株式会社 Anticorrosion coating and anticorrosion coating method
JP3372451B2 (en) * 1997-05-19 2003-02-04 日新製鋼株式会社 Photocatalyst-coated metal plate and method for producing the same
JPH11181339A (en) * 1997-12-22 1999-07-06 Toto Ltd Hydrophilic coating composition
JPH11276562A (en) * 1998-03-26 1999-10-12 Mitsubishi Paper Mills Ltd Absorptive catalyzer compound sheet
JP2000000103A (en) * 1998-06-17 2000-01-07 Nichiban Kenkyusho:Kk Shoe insole and its manufacture
JP2000107610A (en) * 1998-08-03 2000-04-18 Toto Ltd Substrate for photocatalyst deodorization body and photocatalytic deodorization body provided with the same
JP3797037B2 (en) * 1998-12-04 2006-07-12 東陶機器株式会社 Photocatalytic hydrophilic coating composition
JP2000169755A (en) * 1998-12-07 2000-06-20 Jsr Corp Hydrophilic cured material, laminate containing hydrophilic cured material, composition for hydrophilic cured material, and manufacture of hydrophilic cured material
JP4552250B2 (en) * 2000-02-10 2010-09-29 堺化学工業株式会社 Paint, coating film formation method and coating film formed by the method
CN1101353C (en) 2000-04-11 2003-02-12 复旦大学 Self-cleaning glass and its production
JP2002212464A (en) * 2001-01-19 2002-07-31 Kawasaki Heavy Ind Ltd Photocatalyst cream and coating method
CN1447133A (en) 2002-03-25 2003-10-08 冠华科技股份有限公司 Anti-reflection coating layer with transparent electric surface layer
CN1579981A (en) 2003-08-12 2005-02-16 台玻长江玻璃有限公司 Method for manufacturing photocatalytic glass
JP2005194321A (en) * 2003-12-26 2005-07-21 Kao Corp Manufacturing process of dispersion
CN1660955A (en) 2004-02-27 2005-08-31 上海拜坡生物科技有限公司 Hydrophilic antifogging self-cleaning spray anent for glass in Nano photocatalyst and preparing method
EP1757365A1 (en) * 2004-04-20 2007-02-28 Sumitomo Metal Industries, Ltd. Titanium oxide base photocatalyst, process for producing the same and use thereof
JP2006297351A (en) * 2005-04-25 2006-11-02 Showa Denko Kk Photocatalyst film and manufacturing method
JP2006335895A (en) * 2005-06-02 2006-12-14 Sumitomo Dow Ltd Flame-retardant polycarbonate resin composition excellent in light reflectivity and light-reflecting plate comprising the same
EP1873202B1 (en) * 2006-06-29 2009-02-11 Clariant Finance (BVI) Limited Transparent zeolite-polymer hybrid material with tunable properties

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6680135B2 (en) * 1995-09-15 2004-01-20 Saint-Gobain Glass France Substrate with a photocatalytic coating
US6020419A (en) * 1998-03-18 2000-02-01 Bayer Aktiengesellschaft Transparent coating compositions containing nanoscale particles and having improved scratch resistance
US20020045010A1 (en) * 2000-06-14 2002-04-18 The Procter & Gamble Company Coating compositions for modifying hard surfaces

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103042770A (en) * 2012-09-14 2013-04-17 泉耀新材料科技(苏州)有限公司 Building material glass of Titanium dioxide coating film with porosity structure and low refractive index
US10543061B2 (en) 2014-10-03 2020-01-28 3M Innovative Properties Company Methods for managing the scattering of incident light and articles created therefrom

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