WO2014004840A1 - Hydrophobic and oleophobic coating composition - Google Patents

Hydrophobic and oleophobic coating composition Download PDF

Info

Publication number
WO2014004840A1
WO2014004840A1 PCT/IB2013/003262 IB2013003262W WO2014004840A1 WO 2014004840 A1 WO2014004840 A1 WO 2014004840A1 IB 2013003262 W IB2013003262 W IB 2013003262W WO 2014004840 A1 WO2014004840 A1 WO 2014004840A1
Authority
WO
WIPO (PCT)
Prior art keywords
coating composition
composition according
mixture
coating
acid
Prior art date
Application number
PCT/IB2013/003262
Other languages
French (fr)
Other versions
WO2014004840A9 (en
Inventor
Xinyu LIANG
Lifei Hao
Yu Yang
Minhao SONG
KeFeng XIA
Original Assignee
3M Innovative Properties Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 3M Innovative Properties Company filed Critical 3M Innovative Properties Company
Priority to JP2015542079A priority Critical patent/JP2015534601A/en
Priority to US14/411,199 priority patent/US9382441B2/en
Priority to BR112014032893A priority patent/BR112014032893A2/en
Priority to EP13888508.2A priority patent/EP2882817A4/en
Publication of WO2014004840A1 publication Critical patent/WO2014004840A1/en
Publication of WO2014004840A9 publication Critical patent/WO2014004840A9/en

Links

Classifications

    • 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
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/02Homopolymers or copolymers of acids; Metal or ammonium salts thereof
    • 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
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/16Halogen-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/092Polycarboxylic acids
    • 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
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/08Homopolymers or copolymers of acrylic acid esters
    • 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
    • C09D183/00Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04Polysiloxanes
    • C09D183/08Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
    • 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
    • C03C2217/76Hydrophobic and oleophobic coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/22Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/24Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-containing groups

Definitions

  • the disclosure relates to a coating composition, especially a hydrophobic and oleophobic coating composition.
  • Hydrophobic/oleophobic coating is commonly supposed to be the best way of precautions against above issues.
  • the some of the existing hydrophobic/oleophobic coating technologies still remain unsolved problems, like high curing temperature, such as around 150°C, complex process and makes it difficult to be used in the automobile repairing centers.
  • some of coatings have poor durable hydrophobicity.
  • the object of the disclosure is to provide a hydrophobic/oleophobic coating composition with long lasting hydrophobicity by taking following approaches to deal with the above problems mentioned in the background art.
  • the coating composition according to the present disclosure comprises the following components by weight of: 0.1-15% fluorosiloxane, 1-30% polyacrylic resin,
  • the fluorosiloxane is that represented by the formula (I): CF 3 (CF 2 ) a (CH 2 ) b -Si(OCH 2 CH 3 ) 3 (I)
  • a is 3-10, and b is 1-7.
  • the fluorosilane is perfluoro polyether siloxane.
  • the fluorosiloxane is perfluoro polyether siloxane represented by formula (II):
  • the silane coupler is at least one selected from the group consisting of the following compounds:
  • the silane coupler is:
  • the polyacrylic resin is in the form of hydroxy modified polyacrylic resin emulsion.
  • the organic solvent is selected from C 2 _ 3 alcohols, C 2 _ 3 ketones or C 2 _ 3 esters.
  • the organic solvent is ethanol or isopropanol.
  • the organic solvent is acetone or methyl ethyl ketone.
  • the acid is one or more selected from the group consisting of hydrochloric acid, sulfuric acid, acetic acid, citric acid and lactic acid.
  • Another object of the present disclosure is to provide a method to prepare the above coating composition. The method comprises the following steps:
  • the mixture after adding acid into the mixture, the mixture is stirred for 1-3 hrs.
  • the mixture after stirring, the mixture is allowed to stand for aging for at least 1 day.
  • the method for preparing the above coating composition comprises: mixing the fluorosiloxane and acid to obtain a first component, and mixing the organic solvent, the polyacrylic resin and the silane coupler to obtain a second component, and then mixing the first component and the second component, followed by stirring and aging until it is clear.
  • Yet another object of the present disclosure is to provide a use of the above coating composition on surfaces of substrates, such as automotive paints, metals, plastics and glass.
  • hydrophobic and oleophobic coating according to the present disclosure uses
  • the coating composition can form hard coating with high glossiness and high transparency under relatively low temperatures, having a contact angle of 1 15-120°.
  • This coating composition can be used on surfaces of substrates, such as automotive paints, metals, plastics and glass, and it can retain long lasting hydrophobic and oleophobic property even placed outdoors for several months, and it can also prevent the surface of the substrate from being scratched.
  • Fig 1 is the appearance comparison between the coated paint surface with the coating formed from the coating composition according to the present diclosure and the uncoated paint surface.
  • Fig 2 is the transparency comparison between the glass plate coated with the coating according to the present disclosure containing the silane coupler and the glass plate coated with the coating without the silane coupler.
  • Fig 3 shows the standing conditions of water droplets on the coated substrate surface with coating according to the disclosure and uncoated substrate surface.
  • Fig 4 is the schematic figure showing the roll-off angle measuring process for one example sample of the coating composition.
  • Fig 5 is a figure showing the hydrophobicity measuring results for one example sample of the coating composition.
  • Fig 6 shows the durable hydrophobicity results for the coatings containing the polyacrylic resin and not.
  • Fig 7 shows the antifouling (dry ash) test results for one example sample of the coating composition.
  • Figs 8(a)-8(c) show antifouling (wet ash) test results for examples of the coating composition.
  • the coating composition is illustrated by referring to some specific examples below. In the context, unless otherwise indicated, the units of all contents are weight percentage.
  • the hydrophobic and oleophobic coating composition comprises the following components by weight percentage: 0.1-15% perfluoro polyether siloxane, 1- 30% polyacrylic resin, 0.1-15% silane coupler, 33-98% organic solvent, and 0.05-15% acid.
  • the hydrophobic and oleophobic coating according to the present disclosure uses perfluoro polyether siloxane, polyacrylic resin, silane coupler, organic solvent, and acid catalyst.
  • the combination of the polyacrylic resin and perfluoro polyether siloxane which performances hydrophobic property, not only providing good hydrophobicity, but also ensuring long lasting hydrophobicity of the coating with the help of good bonding of polyacrylic resin with perfluoro polyether siloxane.
  • This coating composition can form hard coating with high glossiness and high transparency under relatively low temperatures, having a contact angle of 1 15-120°.
  • the perfluoro polyether siloxane used in the coating composition exhibits hydrophobic property, and can form transparent coating under low temperatures.
  • the amount of perfluoro polyether siloxane is 0.1- 15%, if the amount is less than 0.1%, the transparency is not desired, and if the amount is above 15%, the hydrophobic property is affected.
  • the perfluoro polyether siloxane used is perfluoro polyether siloxane represented by formula (II)
  • the perfluoro polyether siloxane is perfluoro polyether siloxane represented by formula (II)
  • the polyacrylic resin used in the coating composition has very good adhesion and glossiness, and promotes adhesion of the coating on the substrate through chemically bonding with perfluoro polyether siloxane, and thus improves the durable hydrophobicity. Meanwhile, it effectively reduces the disadvantage of losing hydrophobic property under UV light for perfluoro polyether siloxane.
  • the amount of polyacrylic resin is 1-30%. If the amount of polyacrylic resin is below 1%, the durable hydrophobicity of the coating is not desired, and if the amount is above 30%, the hydrophobic property is reduced.
  • the silicone coupler used in the coating composition can apparently improves the compatibility of polyacrylic resin with perfluoro polyether siloxane, in order to eventually achieve fully transparent coating.
  • the amount of silicone coupler is 0.1-15%. If the amount is below 0.1%, the transparency of the coating composition is not desired, and if the amount is above 15%, the hydrophobic property of the coating is reduced.
  • the silane coupler is at least one selected from the group consisting of the following compounds:
  • the silane coupler is:
  • the organic solvent used in the coating composition imparts the coating composition good leveling property.
  • the amount of organic solvent is 33-98%, if the amount is below 33%, the leveling property is not desired, affecting the appearance and transparency of the coating, and if the amount is above 98%, it results in sagging in the applying process.
  • the organic solvent is C2-3 alcohol, C2-3 ketone or C2-3 ester. According to a further embodiment, the organic solvent is ethanol or isopropanol, acetone or methyl ethyl ketone. According to an even further embodiment, the organic solvent is ethanol.
  • the acid used in the coating composition primarily acts as catalyst for the hydrolysis of perfluoro polyether siloxane and silane coupler.
  • the amount of acid is 0.05-15%. If the amount is below 0.05%, the catalytic effect is not obvious, affecting the transparency of the coating, and if the amount is above 15%, the hydrophobic property is reduced.
  • the acid used is one or more of the following acids:
  • hydrochloric acid sulfuric acid, acetic acid, citric acid and lactic acid.
  • the acid is hydrochloric acid.
  • the above coating composition can be prepared through the following method:
  • the coating composition can be prepared through the following method:
  • Table 1 shows the starting materials used in the following exampli
  • ECC4000 represents perfluoro polyether siloxane represented by the formula (II) wherein n and m are respectively 9-10.
  • F8261 represents fluorosiloxane represented by the formula (I) wherein a is 3-10 and b is 1-7.
  • Table 2 is the composition of some examples of the coating composition.
  • Carboset the hydroxy modified polyacrylic resin emulsion provided by Lubrizol under
  • No. 10 and 1 1 are comparative examples, No. 10 is the case without polyacrylic resin, and No.
  • the sample has good spreadability on the surface of the substrate, no sagging, no shrinkage cavity, represented by "o".
  • the sample has good spreadability on the surface of the substrate, no obvious sagging, a small amount of shrinkage cavity, represented by " ⁇ ".
  • the cured coating exhibits transparency as colorless glass, no hazing or blanching phenomena, represented by "o".
  • the cured coating exhibits transparency as colorless glass, minor hazing and blanching phenomena, represented by " ⁇ ".
  • the cured coating is flat, smooth, no shrinkage cavity, no blanching phenomena, represented by "o".
  • the cured coating is flat, smooth, a small amount of shrinkage cavity, minor blanching phenomena, represented by " ⁇ ".
  • Fig 1 is the appearance comparison between the coated paint surface with the coating formed from the coating composition of one example (Example lb) of the coating composition and the uncoated paint surface.
  • the appearance of the paint metal plates before and after coating wherein the plate on the left is the paint metal plate before coating, and the plate on the right is the paint metal plate after coating. It can be seen from the figure 1 that the coating can increase the depth of the color of the paint surface, and make the paint surface seem more black and shining.
  • silane coupler especially KH560
  • the addition of silane coupler modified the compatibility between the polyacrylic resin and fluorosiloxane (for example, ECC4000).
  • Fig 3 shows the hydrophobicity and oleophobicity testing results for the coating of one example (Example lb) of the invention.
  • the shapes of water droplets are different in standing conditions on the paint surface and on glass.
  • the water droplet on the right side of the substrate had a bead- like shape having a contact angle of 1 15°- 120° due to the presence of coating, demonstrating good hydrophobic property.
  • the shape of water droplets on the left had a large contact surface with the blank substrate, having a contact angle of 45-60°, demonstrating poor hydrophobic property.
  • Test example 3 Roll-off angle
  • the roll-off angle is another important indicator of the
  • Roll-off angle is that for the water droplets added on the surface of the substrate to begin to roll off when the substrate is inclined.
  • Fig 6 is the schematic figure showing the roll-off angle measuring process and results for one example (Example lb) of the coating composition.
  • Water droplets with different weights were added on the two parts of the substrate coated (right side) with the coating composition of the invention and uncoated (left side), then the paint substrate is gradually inclined from the horizontal state.
  • the water droplets on the right half coated side would roll off immediately as soon as the substrate was sloped by 10 degrees. However, it was not until 45 degrees that the first droplet on the left uncoated part begun to slide off when all of drops on the right part have rolled off. Even the substrate was erected by 90 degrees, there were still droplets left on the uncoated part.
  • This demonstration indicated that the coating formed by the coating composition according to the present disclosure has excellent hydrophobic property.
  • Test example 4 Oleophobic property
  • the oleophobic property is measured by making a sign on the coated glass plates and uncoated glass plates using oil based marker.
  • the evaluation results for each example were shown in Table 3. Evaluation method:
  • Fig 5 shows the test results for one example (Example lb) of the invention.
  • the left part is the uncoated glass plate, and the right part is coated one with the coating composition.
  • An oil based marker is used to make any sign on the coated and uncoated glass plate. It can be seen from the figure that it was very hard for oil based maker to make a sign on the right coated part, which proved the coating indeed can deliver the olephobic benefits, while it was easy for oil based maker to make a sign on the left uncoated glass plate.
  • Test example 5 Durable hydrophobic property
  • the coated substrate was put outdoors under natural environment such as
  • Fig 6 shown the comparison results for the coating without acrylic resin (Example 10) and the sample with polyacrylic resin and ECC4000 (Example lb).
  • Test example 6 Antifouling property
  • Fig 7 shown the comparison results between the coated paint substrate with the coating (Example lb) and the uncoated paint substrate
  • Test example 7 Wet soil antifouling property
  • Fig 8 shows the comparison results between the lacquer plates with and without the coating.
  • the water-repelling angle of the coating exhibits slow increasing trend. After 5000 times of friction, the coating formed from the coating composition had a water-repelling angle decreased to 100 degrees. Compared to the uncoated substrate, it still retained certain hydrophobic effects.
  • the hydrophobic and oleophobic coating composition used perfluoro polyether siloxane, polyacrylic resin, silane coupler, organic solvent, and acid catalyst.
  • the coating composition can form hard coating with high glossiness and high transparency under relatively low temperatures, having a contact angle of 1 15-120°, exhibiting good hydrophobic property and abrasion resistance.
  • the coating composition can be used on surfaces of substrates, such as automotive paints, metals, plastics and glass, and it can retain long lasting hydrophobic and oleophobic property even placed outdoors for several months, and it can also prevent the surface of the substrate from being scratched.
  • substrates such as automotive paints, metals, plastics and glass

Abstract

The present disclosure provides a hydrophobic and oleophobic coating composition, which comprises the following components based on weight percentage: 0.1-15% of a fluorosiloxane, 1-30% of a polyacrylic resin, 0.1-15% of a silane coupler, 33-98% of an organic solvent, and 0.05-15% of an acid. By combining the polyacrylic resin and the fluorosiloxane which exhibits hydrophobic property, the present composition not only provides good hydrophobic property but also ensures durable hydrophobic property of the coating with the help of good adhesion of polyacrylic resin. The coating composition can form hard coating which has high glossiness and high transparency under relatively low temperatures and has a contact angle of 115-120. This coating composition can be used on surfaces of substrates, such as automotive paints, metal, plastic and glass, and it can retain long lasting hydrophobic and oleophobic property even placed outdoors for several months, and it can also prevent the surface of the substrate from being scratched.

Description

HYDROPHOBIC AND OLEOPHOBIC COATING COMPOSITION
Technical Field
The disclosure relates to a coating composition, especially a hydrophobic and oleophobic coating composition.
Background Art
According to one recent survey of car owners, 64% of respondents thought that the hazy sight in rainy days was the most serious pain. In addition, car is always under harsh conditions and it will be subjected to scratches, stone-chips from flying debris, bugs, acid rain which will attack the car paint with its chemical reactions. This pain damage will devalue the vehicle, affect its beauty and cause the expensive repairs. Similarly, some other fields, for example, building and furniture, are also faced with these issues.
Hydrophobic/oleophobic coating is commonly supposed to be the best way of precautions against above issues. The some of the existing hydrophobic/oleophobic coating technologies still remain unsolved problems, like high curing temperature, such as around 150°C, complex process and makes it difficult to be used in the automobile repairing centers. In addition, some of coatings have poor durable hydrophobicity.
Therefore, there is still a need to provide a hydrophobic and oleophobic coating composition with long lasting hydrophobic property and simple process.
Summary of the disclosure
The object of the disclosure is to provide a hydrophobic/oleophobic coating composition with long lasting hydrophobicity by taking following approaches to deal with the above problems mentioned in the background art.
To achieve the above object, the coating composition according to the present disclosure comprises the following components by weight of: 0.1-15% fluorosiloxane, 1-30% polyacrylic resin,
0.1- 15% silane coupler, 33-98% organic solvent, and 0.05- 15% acid.
According to certain embodiments, the fluorosiloxane is that represented by the formula (I): CF3(CF2)a(CH2)b-Si(OCH2CH3)3 (I)
Wherein, a is 3-10, and b is 1-7.
According to certain embodiments, the fluorosilane is perfluoro polyether siloxane.
According to certain embodiments, the fluorosiloxane is perfluoro polyether siloxane represented by formula (II):
(C2H50)3Si(CH2)3N(H(C(0)-RrC(0)N(H)(CH2)3Si(OC2H5)3 (II) wherein Rf is CF20(CF2CF20)n(CF20) m CF2, n and m are independently 1 -20. More preferably, n and m are independently 9 and 10.
According to certain embodiments, the silane coupler is at least one selected from the group consisting of the following compounds:
2H5
Figure imgf000004_0001
and CH2=C(CH3)COOC3H6Si(OCH3).
According to certain embodiments, the silane coupler is:
Figure imgf000004_0002
According to certain embodiments, the polyacrylic resin is in the form of hydroxy modified polyacrylic resin emulsion.
According to certain embodiments, the organic solvent is selected from C2_3 alcohols, C2_3 ketones or C2_3 esters.
According to certain embodiments, the organic solvent is ethanol or isopropanol.
According to certain embodiments, the organic solvent is acetone or methyl ethyl ketone.
According to certain embodiments, the acid is one or more selected from the group consisting of hydrochloric acid, sulfuric acid, acetic acid, citric acid and lactic acid. Another object of the present disclosure is to provide a method to prepare the above coating composition. The method comprises the following steps:
mixing the organic solvent, the polyacrylic resin, the silane coupler and the fluorosiloxane to yield a clear mixture;
adding acid into the mixture, and stirring it until the mixture is clear;
allowing the mixture to stand for aging.
According to certain embodiments, in the above preparation method, after adding acid into the mixture, the mixture is stirred for 1-3 hrs.
According to certain embodiments, in the above preparation method, after stirring, the mixture is allowed to stand for aging for at least 1 day.
According to certain embodiments, the method for preparing the above coating composition, comprises: mixing the fluorosiloxane and acid to obtain a first component, and mixing the organic solvent, the polyacrylic resin and the silane coupler to obtain a second component, and then mixing the first component and the second component, followed by stirring and aging until it is clear.
Yet another object of the present disclosure is to provide a use of the above coating composition on surfaces of substrates, such as automotive paints, metals, plastics and glass.
The hydrophobic and oleophobic coating according to the present disclosure uses
fluorosiloxane, polyacrylic resin, silicone coupler, organic solvent, and acid catalyst. The combination the polyacrylic resin and fluorosiloxane which performances hydrophobicity, not only providing good hydrophobic property, but also ensuring long lasting hydrophobicity of the coating with the help of good bonding of polyacrylic resin. In particular, using perfluoro polyether siloxane, the coating composition can form hard coating with high glossiness and high transparency under relatively low temperatures, having a contact angle of 1 15-120°. This coating composition can be used on surfaces of substrates, such as automotive paints, metals, plastics and glass, and it can retain long lasting hydrophobic and oleophobic property even placed outdoors for several months, and it can also prevent the surface of the substrate from being scratched. Description of the Drawings
Fig 1 is the appearance comparison between the coated paint surface with the coating formed from the coating composition according to the present diclosure and the uncoated paint surface.
Fig 2 is the transparency comparison between the glass plate coated with the coating according to the present disclosure containing the silane coupler and the glass plate coated with the coating without the silane coupler.
Fig 3 shows the standing conditions of water droplets on the coated substrate surface with coating according to the disclosure and uncoated substrate surface.
Fig 4 is the schematic figure showing the roll-off angle measuring process for one example sample of the coating composition.
Fig 5 is a figure showing the hydrophobicity measuring results for one example sample of the coating composition.
Fig 6 shows the durable hydrophobicity results for the coatings containing the polyacrylic resin and not.
Fig 7 shows the antifouling (dry ash) test results for one example sample of the coating composition.
Figs 8(a)-8(c) show antifouling (wet ash) test results for examples of the coating composition.
Detailed description of the embodiment
The coating composition is illustrated by referring to some specific examples below. In the context, unless otherwise indicated, the units of all contents are weight percentage.
According to the present disclosure, the hydrophobic and oleophobic coating composition comprises the following components by weight percentage: 0.1-15% perfluoro polyether siloxane, 1- 30% polyacrylic resin, 0.1-15% silane coupler, 33-98% organic solvent, and 0.05-15% acid.
The hydrophobic and oleophobic coating according to the present disclosure uses perfluoro polyether siloxane, polyacrylic resin, silane coupler, organic solvent, and acid catalyst. The combination of the polyacrylic resin and perfluoro polyether siloxane which performances hydrophobic property, not only providing good hydrophobicity, but also ensuring long lasting hydrophobicity of the coating with the help of good bonding of polyacrylic resin with perfluoro polyether siloxane. This coating composition can form hard coating with high glossiness and high transparency under relatively low temperatures, having a contact angle of 1 15-120°.
The perfluoro polyether siloxane used in the coating composition exhibits hydrophobic property, and can form transparent coating under low temperatures. In the coating composition, the amount of perfluoro polyether siloxane is 0.1- 15%, if the amount is less than 0.1%, the transparency is not desired, and if the amount is above 15%, the hydrophobic property is affected.
According to a certain embodiment, the perfluoro polyether siloxane used is perfluoro polyether siloxane represented by formula (II)
(C2H50)3Si(CH2)3N(H(C(0)-RrC(0)N(H)(CH2)3Si(OC2H5)3 (II) wherein, Rf is CF20(CF2CF20)n(CF20) m CF2, n and m are independently 1-20.
According to a further embodiment, the perfluoro polyether siloxane is perfluoro polyether siloxane represented by formula (II)
(C2H50)3Si(CH2)3N(H(C(0)-RrC(0)N(H)(CH2)3Si(OC2H5)3 (II) wherein, Rf is CF20(CF2CF20)n(CF20) m CF2, n and m are independently 9 and 10, and the molecular weight is around 2400.
The polyacrylic resin used in the coating composition has very good adhesion and glossiness, and promotes adhesion of the coating on the substrate through chemically bonding with perfluoro polyether siloxane, and thus improves the durable hydrophobicity. Meanwhile, it effectively reduces the disadvantage of losing hydrophobic property under UV light for perfluoro polyether siloxane. In the coating composition according to the present disclosure, the amount of polyacrylic resin is 1-30%. If the amount of polyacrylic resin is below 1%, the durable hydrophobicity of the coating is not desired, and if the amount is above 30%, the hydrophobic property is reduced.
The silicone coupler used in the coating composition can apparently improves the compatibility of polyacrylic resin with perfluoro polyether siloxane, in order to eventually achieve fully transparent coating. In the coating composition, the amount of silicone coupler is 0.1-15%. If the amount is below 0.1%, the transparency of the coating composition is not desired, and if the amount is above 15%, the hydrophobic property of the coating is reduced. According to certain embodiments, the silane coupler is at least one selected from the group consisting of the following compounds:
Figure imgf000008_0001
I
NH3— C H3— C H3— C H3— 3 i-OC 2H5
I
OC2H5
and CH2=C(CH3)COOC3H6Si(OCH3).
According to a further embodiment, the silane coupler is:
Figure imgf000008_0002
The organic solvent used in the coating composition imparts the coating composition good leveling property. In the coating composition, the amount of organic solvent is 33-98%, if the amount is below 33%, the leveling property is not desired, affecting the appearance and transparency of the coating, and if the amount is above 98%, it results in sagging in the applying process.
According to certain embodiments the organic solvent is C2-3 alcohol, C2-3 ketone or C2-3 ester. According to a further embodiment, the organic solvent is ethanol or isopropanol, acetone or methyl ethyl ketone. According to an even further embodiment, the organic solvent is ethanol.
The acid used in the coating composition primarily acts as catalyst for the hydrolysis of perfluoro polyether siloxane and silane coupler. In the coating composition, the amount of acid is 0.05-15%. If the amount is below 0.05%, the catalytic effect is not obvious, affecting the transparency of the coating, and if the amount is above 15%, the hydrophobic property is reduced. According to certain embodiments, the acid used is one or more of the following acids:
hydrochloric acid, sulfuric acid, acetic acid, citric acid and lactic acid. According to a further embodiment, the acid is hydrochloric acid.
The above coating composition can be prepared through the following method:
mixing the organic solvent, the polyacrylic resin, the silane coupler and the perfluoro polyether siloxane to yield a clear mixture;
adding acid into the mixture, and stirring it until the mixture is clear;
allowing the mixture to stand for aging, until it is completely clear.
The coating composition can be prepared through the following method:
mixing the perfluoro polyether siloxane and acid as a first component, and mixing the organic solvent, the polyacrylic resin and the silane coupler as a second component, and then mixing the first component and the second component, followed by stirring and aging until it is completely clear.
Examples
Table 1 shows the starting materials used in the following exampli
Table 1
Figure imgf000009_0001
ECC4000 represents perfluoro polyether siloxane represented by the formula (II) wherein n and m are respectively 9-10.
F8261 represents fluorosiloxane represented by the formula (I) wherein a is 3-10 and b is 1-7. Table 2 is the composition of some examples of the coating composition.
Table 2 The composition of the examples, wt%
Figure imgf000010_0001
Carboset: the hydroxy modified polyacrylic resin emulsion provided by Lubrizol under
Carboset ®GA1594[CST1594].
No. 10 and 1 1 are comparative examples, No. 10 is the case without polyacrylic resin, and No.
1 1 is the case without silane coupler.
If polyacrylic resin is not added, durable hydrophobic property and abrasion resistance cannot be assured; if the amount of silane coupler is not sufficient or without addition, the transparency of the film would be greatly reduced. Table 3 Test results of the example coatings
Figure imgf000011_0001
o : good, Δ: relatively good, x: poor. Experiment Process
1) Cleaning the surface of the substrate with ethyl alcohol.
2) Adding ethanol, polyacrylic resin, silane coupler, HCl, ECC4000 sequentially, and stirring for 1 -3 h.
3) Allowing the mixture to stand for aging for 1 day, and then the mixture is in clear state.
4) Applying the sample on the substrate, and placing the substrate into an oven to stand for 2-24 h at 30-40°C. Under the condtion of 80°C, it takes 15-20 mins to be cured into a film.
Test Example 1 : Appearance of coating modification
There were two crucial factors closely related to the final appearance of coating: the leveling property of sample and the transparency of coating after curing. The samples were subjected to visual measurement for the leveling property, the color and transparency of the coating after curing, and the evaluation results for each example were shown in Table 3. Evaluation method:
1. Leveling property
Good: The sample has good spreadability on the surface of the substrate, no sagging, no shrinkage cavity, represented by "o".
Relatively good: The sample has good spreadability on the surface of the substrate, no obvious sagging, a small amount of shrinkage cavity, represented by "Δ".
Poor: The sample has poor spreadability on the surface of the substrate, obvious sagging, severe shrinkage cavity, represented by "x".
2. Transparency
Good: The cured coating exhibits transparency as colorless glass, no hazing or blanching phenomena, represented by "o".
Relatively good: The cured coating exhibits transparency as colorless glass, minor hazing and blanching phenomena, represented by "Δ".
Poor: The cured coating is matte and opaque, represented by "x".
3. Appearance
Good: The cured coating is flat, smooth, no shrinkage cavity, no blanching phenomena, represented by "o".
Relatively good: The cured coating is flat, smooth, a small amount of shrinkage cavity, minor blanching phenomena, represented by "Δ".
Poor: The cured coating is not flat, rough, opaque, shrinkage cavity, represented by "x". The property test results of some examples are illustrated as follows by referring to the drawings.
Fig 1 is the appearance comparison between the coated paint surface with the coating formed from the coating composition of one example (Example lb) of the coating composition and the uncoated paint surface. The appearance of the paint metal plates before and after coating, wherein the plate on the left is the paint metal plate before coating, and the plate on the right is the paint metal plate after coating. It can be seen from the figure 1 that the coating can increase the depth of the color of the paint surface, and make the paint surface seem more black and shining.
One feature of the coating composition is that the addition of silane coupler, especially KH560, largely improves the transparency of the coating. As for the glass substrates shown in Fig 2, the glass plate (a) shown the coating coated with the composition without silane coupler (Example 1 1) was white and opaque. The glass plate (b) shown that the coating with coated with composition containing silane coupler (Example lb) was highly transparent. The reason might be as follows: the addition of silane coupler modified the compatibility between the polyacrylic resin and fluorosiloxane (for example, ECC4000).
Test example 2: Contact angle
Contact angle analyser DSA100E was used to measure the contact angle of each sample. The measuring results for each example were shown in Table 3.
Fig 3 shows the hydrophobicity and oleophobicity testing results for the coating of one example (Example lb) of the invention.
As shown in Fig 3, the shapes of water droplets are different in standing conditions on the paint surface and on glass. The water droplet on the right side of the substrate had a bead- like shape having a contact angle of 1 15°- 120° due to the presence of coating, demonstrating good hydrophobic property. However, the shape of water droplets on the left had a large contact surface with the blank substrate, having a contact angle of 45-60°, demonstrating poor hydrophobic property. Test example 3 : Roll-off angle
Besides the contact angle, the roll-off angle is another important indicator of the
hydrophobicity. Roll-off angle is that for the water droplets added on the surface of the substrate to begin to roll off when the substrate is inclined. The measuring results for each example were shown in Table 3.
Fig 6 is the schematic figure showing the roll-off angle measuring process and results for one example (Example lb) of the coating composition. Water droplets with different weights were added on the two parts of the substrate coated (right side) with the coating composition of the invention and uncoated (left side), then the paint substrate is gradually inclined from the horizontal state. The water droplets on the right half coated side would roll off immediately as soon as the substrate was sloped by 10 degrees. However, it was not until 45 degrees that the first droplet on the left uncoated part begun to slide off when all of drops on the right part have rolled off. Even the substrate was erected by 90 degrees, there were still droplets left on the uncoated part. This demonstration indicated that the coating formed by the coating composition according to the present disclosure has excellent hydrophobic property.
Test example 4: Oleophobic property
The oleophobic property is measured by making a sign on the coated glass plates and uncoated glass plates using oil based marker. The evaluation results for each example were shown in Table 3. Evaluation method:
Good: with essentially no track, represented by "o".
Relatively good: no obvious track, represented by "Δ".
Poor: with obvious track, represented by "x".
Fig 5 shows the test results for one example (Example lb) of the invention. As shown in Fig 5, the left part is the uncoated glass plate, and the right part is coated one with the coating composition. An oil based marker is used to make any sign on the coated and uncoated glass plate. It can be seen from the figure that it was very hard for oil based maker to make a sign on the right coated part, which proved the coating indeed can deliver the olephobic benefits, while it was easy for oil based maker to make a sign on the left uncoated glass plate.
Test example 5: Durable hydrophobic property
Measuring method: the coated substrate was put outdoors under natural environment such as
UV, raining and dust etc, a periodic contact angle measurement is carried out.
The sample is placed outdoors for the periodic measurement. The time is recorded when the hydrophobic property is completely lost. The evaluation results for each example were shown in Table 3.
Evaluation Method:
Good: contact angle above 100 degrees, represented by "o".
Relatively good: contact angle above 90 degrees, represented by "Δ".
Poor: contact angle below 90 degrees, represented by "x".
Fig 6 shown the comparison results for the coating without acrylic resin (Example 10) and the sample with polyacrylic resin and ECC4000 (Example lb).
As shown in Fig 6, because ECC4000 is not UV resistant, the sample without polyacrylic resin completely loses hydrophobic property after two months. However, for the sample containing polyacrylic resin, the hydrophobic property can be maintained longer. This indicates that polyacrylic resin promotes the structural stability of ECC4000, especially improves the UV resistant capability.
Test example 6: Antifouling property
The samples were placed into a sealed can with a standard soil, shaken up and down for 100 times before being taken out. After shaking off the drifting dust, the ash staining effects on the surface were observed. The evaluation results for each example were shown in Table 3.
Evaluation method:
Good: without obvious dirty mark, represented by "o".
Relatively good: with a small amount of dirty marks, represented by "Δ".
Poor: with obvious dirty mark, represented by "x". Fig 7 shown the comparison results between the coated paint substrate with the coating (Example lb) and the uncoated paint substrate
As can be seen from Fig 7, on the left coated substrate with the coating, the amount of the adhered ash was far below that of the right uncoated substrate. This indicated that the hydrophobic coating had obvious dry ash resistance effects.
Test example 7: Wet soil antifouling property
Because fouling is always a mixture of water and dust in the practical environment, we had developed a wet soil spraying method to further evaluate the antifouling property of the hydrophobic coating.
14 g standard soil and 700 g water were mixed, and sprayed on the substrate, and the substrate was allowed to stand for 10 mins, before they were put into an oven and stored at 50°C for 10 mins. After this process was repeated 3 times, the substrate was cooled and washed with tap water. The antifouling property was evaluated based on the adhesion condition of the surface fouling after washing. The standard soil is commercial available from Gorecki Manufacture, USA. The evaluation results for each example were shown in Table 3.
Evaluation method:
Good: without obvious dirty mark, represented by "o".
Relatively good: with a small amount of dirty marks, represented by "Δ".
Poor: with obvious dirty mark, represented by "x".
Fig 8 shows the comparison results between the lacquer plates with and without the coating.
As shown in Fig 8(a), before spraying, the coating on the left was obviously blacker and brighter than the one on the right. After 3 turns of wet soil spraying, the soil adhesion amount of the uncoated substrate was obviously higher than that of the coated substrate, as shown in Fig 8(b). Even after washing with clean water for the same time period, the uncoated substrate still had more soil deposition, as shown in Fig 8 (c). Overall, the coating had very good antifouling property. Test example 8: Abrasion resistance
Wet abrasion test was carried out on REF903 (friction machine). After friction, the changes on the water-repelling angle were measured. The evaluation results for each example were shown in Table 3.
As the number of abrasion times increases, the water-repelling angle of the coating exhibits slow increasing trend. After 5000 times of friction, the coating formed from the coating composition had a water-repelling angle decreased to 100 degrees. Compared to the uncoated substrate, it still retained certain hydrophobic effects.
The hydrophobic and oleophobic coating composition used perfluoro polyether siloxane, polyacrylic resin, silane coupler, organic solvent, and acid catalyst. The combination of polyacrylic resin and perfluoro polyether siloxane which performances hydrophobic property, not only ensures good hydrophobic property, but also ensures long lasting hydrophobic property of the coating with the help of good adhesion of polyacrylic resin. The coating composition can form hard coating with high glossiness and high transparency under relatively low temperatures, having a contact angle of 1 15-120°, exhibiting good hydrophobic property and abrasion resistance. The coating composition can be used on surfaces of substrates, such as automotive paints, metals, plastics and glass, and it can retain long lasting hydrophobic and oleophobic property even placed outdoors for several months, and it can also prevent the surface of the substrate from being scratched.

Claims

What is claimed is:
1. A coating composition, which comprises the following components based on weight percentage:
0.1 - 15% of a fluorosiloxane,
1-30% of a polyacrylic resin,
0.1- 15% of a silane coupler,
0.05- 15% of an acid, and
33-98% of an organic solvent.
2. The coating composition according to claim 1 , characterized in that the fluorosiloxane is represented by the formula (I):
CF3(CF2)a(CH2)b-Si(OCH2CH3)3 (D
wherein, a is 3- 10, and b is 1-7.
3. The coating composition according to claim 1 , characterized in that the fluorosilane is perfluoro polyether siloxane.
4. The coating composition according to claim 3, characterized in that the fluorosilane is perfluoro polyether siloxane represented by formula (II):
(C2H50)3Si(CH2)3N(H(C(0)-RrC(0)N(H)(CH2)3Si(OC2H5)3 (II) wherein Rf is CF20(CF2CF20)n(CF20) mCF2, n and m are independently 1-20.
The coating composition according to claim 4, characterized in that n and m are independently
6. The coating composition according to any one of claims 1-5, characterized in that the silane coupler is at least one selected from the group consisting of the following compounds:
Figure imgf000019_0001
OC2H5
I
NH3— C H3— C H3— C H3— 3 i-OC 2H5 and
C(CH3)COOC3H6Si(OCH3).
7. The coatin composition according to claim 6, characterized in that the silane coupler is:
Figure imgf000019_0002
8. The coating composition according to any of claims 1-7, characterized in that the polyacrylic resin is in the form of hydroxy modified polyacrylic resin emulsion.
9. The coating composition according to any of claims 1-8, characterized in that the organic solvent is selected from the group consisting of C2_3 alcohols, C2_3 ketones and C2_3 esters.
10. The coating composition according to claim 9, characterized in that the organic solvent is at least one selected from the group consisting of ethanol and isopropanol.
1 1. The coating composition according to claim 10, characterized in that the organic solvent is at least one selected from the group consisting of acetone and methyl ethyl ketone.
12. The coating composition according to any one of claims 1-1 1, characterized in that the acid is at least one selected from of the group consisting of hydrochloric acid, sulfuric acid, acetic acid, citric acid and lactic acid.
13. A method for preparing the coating composition according to any one of claims 1-12, comprising the following steps:
a) mixing the organic solvent, the polyacrylic resin, the silane coupler and the fluorosiloxane to yield a clear mixture;
b) adding the acid into the mixture, and stirring it until the mixture being clear; and c) allowing the mixture obtained in step b) to stand for aging.
14. The method according to claim 13, characterized in that in step b) the mixture is stirred for 1-3 hrs.
15. The method according to claim 13 or 14, characterized in that in step c) the mixture is aged for at least 1 day.
16. A method for preparing the coating composition according to any of claims 1- 12, comprising: mixing the fluorosiloxane and acid to obtain a first mixture, and mixing the organic solvent, the polyacrylic resin and the silane coupler to obtain a second mixture, and then mixing the first mixture and the second mixture, followed by stirring and aging.
17. The method according to claim 16, characterized in that the stirring takes 1-3 hrs.
18. The method according to claim 16 or 17, characterized in that the aging takes at least 1 day.
19. A use of the coating composition according to any of claims 1-12 on surface of substrate selected from the group consisting of automotive paints, metals, plastics and glass.
PCT/IB2013/003262 2012-06-29 2013-06-27 Hydrophobic and oleophobic coating composition WO2014004840A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2015542079A JP2015534601A (en) 2012-06-29 2013-06-27 Hydrophobic and oleophobic coating composition
US14/411,199 US9382441B2 (en) 2012-06-29 2013-06-27 Hydrophobic and oleophobic coating composition
BR112014032893A BR112014032893A2 (en) 2012-06-29 2013-06-27 hydrophobic and oleophobic coating composition
EP13888508.2A EP2882817A4 (en) 2012-06-29 2013-06-27 Hydrophobic and oleophobic coating composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201210229101.7A CN103509422B (en) 2012-06-29 2012-06-29 A kind of hydrophobic and oleophobic coating composition
CN201210229101.7 2012-06-29

Publications (2)

Publication Number Publication Date
WO2014004840A1 true WO2014004840A1 (en) 2014-01-03
WO2014004840A9 WO2014004840A9 (en) 2014-10-30

Family

ID=49783862

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2013/003262 WO2014004840A1 (en) 2012-06-29 2013-06-27 Hydrophobic and oleophobic coating composition

Country Status (6)

Country Link
US (1) US9382441B2 (en)
EP (1) EP2882817A4 (en)
JP (1) JP2015534601A (en)
CN (1) CN103509422B (en)
BR (1) BR112014032893A2 (en)
WO (1) WO2014004840A1 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016056293A (en) * 2014-09-10 2016-04-21 信越化学工業株式会社 Fluorine-containing coating agent, and article treated with the coating agent
JP2016153221A (en) * 2014-12-26 2016-08-25 大日本印刷株式会社 Composition, member prepared with composition, and method for producing the same, and touch panel comprising member
JP2018510506A (en) * 2015-03-06 2018-04-12 オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツングOsram Opto Semiconductors GmbH Optoelectronic device and method of manufacturing optoelectronic device
WO2019236043A3 (en) * 2018-06-05 2020-02-20 Ataturk Universitesi Bilimsel Arastirma Projeleri Birimi Uv-curable, biocompatible, superamphiphobic coating
EP3842391A1 (en) * 2016-09-01 2021-06-30 Agc Inc. Coated glass substrate
CN113308192A (en) * 2021-07-13 2021-08-27 安徽江锐新材料有限公司 Heat-resistant organic silicon high-temperature-resistant primer and preparation process thereof

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104804148A (en) * 2015-05-05 2015-07-29 湖南晟通纳米新材料有限公司 Fluorosilicone acrylate emulsion and preparing method of fluorosilicone acrylate emulsion
CN106189598B (en) * 2016-08-11 2018-08-14 无锡市虎皇漆业有限公司 Double thin sand textured coatings and preparation method thereof
CN108300303A (en) * 2016-09-28 2018-07-20 卢火青 The hydrophobic dust-proof nano coating composition and its preparation method and application of high-transmission rate
EP3587366B1 (en) 2017-02-21 2023-09-13 AGC Inc. Glass plate and manufacturing method of glass plate
CN107022287A (en) * 2017-06-08 2017-08-08 苏州蓝锐纳米科技有限公司 A kind of fluorinated hydrophobic minute surface nano paint and preparation method thereof
CN107057542A (en) * 2017-06-08 2017-08-18 苏州蓝锐纳米科技有限公司 A kind of minute surface nano paint using trimethylene carbonate as monomer
CN107022288A (en) * 2017-06-08 2017-08-08 苏州蓝锐纳米科技有限公司 A kind of electronic industry minute surface antifriction nano-coating and preparation method thereof
BR112020004024B1 (en) 2017-09-27 2023-01-31 Kimberly-Clark Worldwide, Inc. DISPENSER FOR DISPENSING ABSORBENT PRODUCT, AND, METHOD
CN109897485A (en) * 2019-01-31 2019-06-18 苏州百联节能科技股份有限公司 A kind of self-cleaning environmental protection coating material of novel heat-insulation
CN111732345A (en) * 2020-06-29 2020-10-02 几何智慧城市科技(广州)有限公司 Method for rapidly preparing transparent super-hydrophobic composite coating at normal temperature
CN114054319A (en) * 2020-07-30 2022-02-18 深圳市万普拉斯科技有限公司 Coating structure, preparation method thereof, material product comprising coating structure and electronic product
RU2763134C1 (en) * 2020-09-15 2021-12-27 Иван Соломонович Пятов Filter element for filtration of a liquid
CN113121808B (en) * 2021-04-02 2022-12-13 汕头大学 Fluorine-silicon modified multifunctional flax oil-based alkyd resin UV curing coating and preparation and application thereof
CN116410625A (en) * 2023-03-13 2023-07-11 东南大学 Modified UV gloss oil and method for preparing transparent antifouling coating based on modified gloss oil

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1555249A1 (en) * 2004-01-15 2005-07-20 Nanogate Coating Systems GmbH Hydrophobic and/or oleophobic coating on microstructured glass surfaces providing an anti-fingerprint effect
US20120029127A1 (en) * 2008-12-31 2012-02-02 Ichia Technologies, Inc. Coating structure, chemical composition for forming the same, and method of forming the same
RU2447113C2 (en) * 2006-06-14 2012-04-10 Эвоник Дегусса Гмбх Scratch-resistant and wear-resistant coatings on polymeric surfaces

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69218811T2 (en) 1991-01-23 1997-07-17 Matsushita Electric Ind Co Ltd Water and oil repellent adsorbed film and process for its manufacture
JPH05170486A (en) * 1991-12-25 1993-07-09 Central Glass Co Ltd Water repellent for glass surface and water-repellent glass
TW376408B (en) * 1995-12-01 1999-12-11 Nissan Chemical Ind Ltd Coating film having water repellency and low refractive index
JP3344199B2 (en) * 1996-03-21 2002-11-11 ソニー株式会社 Antifouling film forming composition and antireflection filter
JPH1017823A (en) * 1996-06-28 1998-01-20 Toray Dow Corning Silicone Co Ltd Coating composition
DE19904132C2 (en) * 1999-02-03 2002-11-28 Degussa Composition of fluoroorganofunctional silanes and siloxanes, process for their preparation and their use
JP3729687B2 (en) * 1999-08-04 2005-12-21 株式会社巴川製紙所 Anti-reflective material
DE19964309C2 (en) * 1999-11-15 2003-07-03 Degussa Triamino and fluoroalkyl functional organosiloxanes or mixtures thereof
US20040191481A1 (en) * 2001-05-31 2004-09-30 Volker Erb Reflective sheet treated with fluorosilane
MXPA04000983A (en) * 2001-08-02 2004-04-20 Clariant Gmbh Fluoroalkyl-modified organosilanes and their use in coating compositions.
JP4887783B2 (en) * 2003-12-18 2012-02-29 日産化学工業株式会社 Coating with low refractive index and water repellency
US7247386B2 (en) * 2003-12-23 2007-07-24 3M Innovative Properties Company Composition of an oligomeric fluorosilane and surface treatment of retroreflective sheet
US7863485B2 (en) * 2004-12-10 2011-01-04 Omnitech Environmental, Llc Additive and vehicle for inks, paints, coatings and adhesives
US7914809B2 (en) * 2005-08-26 2011-03-29 Boston Scientific Scimed, Inc. Lubricious composites for medical devices
US20080221263A1 (en) 2006-08-31 2008-09-11 Subbareddy Kanagasabapathy Coating compositions for producing transparent super-hydrophobic surfaces
US8057907B2 (en) * 2006-03-06 2011-11-15 Fujifilm Corporation Optical film, coating composition, polarizing plate and image display device
TWI384039B (en) * 2006-12-27 2013-02-01 Ind Tech Res Inst Method of fabricating transparent hydrophobic self-cleaning coating material and coating material and transparent coating made therefrom
EP2159261B1 (en) 2007-06-15 2012-12-26 Dow Corning Corporation Curable fluorine-containing polymer composition
US9896549B2 (en) * 2010-04-13 2018-02-20 Aaron Kessman Hydrophobic and oleophobic coatings
US8883314B2 (en) * 2011-01-25 2014-11-11 Corning Incorporated Coated articles with improved fingerprint resistance and methods of making same
CN102417773A (en) * 2011-10-14 2012-04-18 袁志庆 Superhydrophobic acrylic resin paint

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1555249A1 (en) * 2004-01-15 2005-07-20 Nanogate Coating Systems GmbH Hydrophobic and/or oleophobic coating on microstructured glass surfaces providing an anti-fingerprint effect
RU2447113C2 (en) * 2006-06-14 2012-04-10 Эвоник Дегусса Гмбх Scratch-resistant and wear-resistant coatings on polymeric surfaces
US20120029127A1 (en) * 2008-12-31 2012-02-02 Ichia Technologies, Inc. Coating structure, chemical composition for forming the same, and method of forming the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
"Perfomance Coatings. Carboset Acrylic Polymers.", LUBRIZOL, 27 September 2010 (2010-09-27), Retrieved from the Internet <URL:http:lubrizol.com/Coatings/Carboset/default.html> *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016056293A (en) * 2014-09-10 2016-04-21 信越化学工業株式会社 Fluorine-containing coating agent, and article treated with the coating agent
JP2016153221A (en) * 2014-12-26 2016-08-25 大日本印刷株式会社 Composition, member prepared with composition, and method for producing the same, and touch panel comprising member
JP2018510506A (en) * 2015-03-06 2018-04-12 オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツングOsram Opto Semiconductors GmbH Optoelectronic device and method of manufacturing optoelectronic device
US10243110B2 (en) 2015-03-06 2019-03-26 Osram Opto Semiconductors Gmbh Optoelectronic device and method for the production of an optoelectronic device
EP3842391A1 (en) * 2016-09-01 2021-06-30 Agc Inc. Coated glass substrate
WO2019236043A3 (en) * 2018-06-05 2020-02-20 Ataturk Universitesi Bilimsel Arastirma Projeleri Birimi Uv-curable, biocompatible, superamphiphobic coating
CN113308192A (en) * 2021-07-13 2021-08-27 安徽江锐新材料有限公司 Heat-resistant organic silicon high-temperature-resistant primer and preparation process thereof

Also Published As

Publication number Publication date
US20150141563A1 (en) 2015-05-21
US9382441B2 (en) 2016-07-05
JP2015534601A (en) 2015-12-03
CN103509422B (en) 2018-07-31
WO2014004840A9 (en) 2014-10-30
EP2882817A1 (en) 2015-06-17
EP2882817A4 (en) 2016-02-24
CN103509422A (en) 2014-01-15
BR112014032893A2 (en) 2017-06-27

Similar Documents

Publication Publication Date Title
US9382441B2 (en) Hydrophobic and oleophobic coating composition
CN108329480B (en) Modified polysilazane prepolymer, modified polysilazane coating, and method of using same
TWI415912B (en) Polysilazane coatings for metal and polymer surfaces
CN102471640B (en) Surface conditioner for coating agents
US8343631B2 (en) Low-gloss, two-component clear coats, articles of manufacture having low-gloss, two-component clear coats, and methods for applying the same
CN109868073B (en) Color-changing film with self-repairing function and preparation method thereof
CN102911541B (en) Weather-proofing anti-scratch ultraviolet cured hard coating composite
CN109897503A (en) A kind of normal temperature cure modifying epoxy resin by organosilicon coating and the preparation method and application thereof
CN105348498B (en) The aqueous alkide resin of weatherability, water-tolerant
CN103443220A (en) Weather-resistant coating composition, and method for forming coated article having weather-esistant coating film
JP2019183149A (en) Mixed composition
JP6457703B2 (en) Method for producing thin film liquid repellent layer and thin film liquid repellent layer
CN110903761A (en) Preparation method of organic glass surface hardening coating, stock solution formula and preparation method
CN104926148A (en) Antifogging anti-scratch coating and preparation method thereof
JP2022065006A (en) Fluorinated Ester Compound Additives for Architectural Coatings
CN112143276B (en) Antifouling auxiliary agent for automobile varnish and preparation method and application thereof
KR100513825B1 (en) Pollution-prevention advertisement sticker non-sticking coating compositions and the method
CN101868303A (en) An agent for the treatment of top-coat paint films to impart stain resistance and a method for the treatment of top-coat paint films to impart stain-resistance
CN104710847A (en) Anti-sticking cream and preparation method thereof
KR101965706B1 (en) Coating agent composition for preventing sticking of posters, Coating agent for preventing sticking of posters using the same, and Manufacturing method thereof
WO2007119630A1 (en) Planing coat and method for producing the same
JP6910365B2 (en) Partially Fluorinated Ester Compound Additives for Architectural Coatings
KR101038440B1 (en) Hard coating agent for modificating the surface of transparent plastics and method for preparing for the same
KR101846441B1 (en) One-component type matt solvent paint composition for automotive top coating
CN114921170A (en) Anti-fogging UV (ultraviolet) finishing oil for automobile rearview mirror and preparation method thereof

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13808703

Country of ref document: EP

Kind code of ref document: A1

DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)
WWE Wipo information: entry into national phase

Ref document number: 14411199

Country of ref document: US

ENP Entry into the national phase

Ref document number: 2015542079

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

REEP Request for entry into the european phase

Ref document number: 2013888508

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2013888508

Country of ref document: EP

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13888508

Country of ref document: EP

Kind code of ref document: A1

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112014032893

Country of ref document: BR

DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)
ENP Entry into the national phase

Ref document number: 112014032893

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20141229