WO2012148537A1

WO2012148537A1 - Process for forming an anti-fouling coating system

Info

Publication number: WO2012148537A1
Application number: PCT/US2012/026294
Authority: WO
Inventors: Songwei Lu
Original assignee: Ppg Industries Ohio, Inc.
Priority date: 2011-04-29
Filing date: 2012-02-23
Publication date: 2012-11-01

Abstract

Provided is a process for forming a durable anti-fouling coating on a substrate including: (a) modifying a surface of the substrate using a surface modification means; (b) applying a first coating composition to at least a portion of the modified substrate surface to form a first coating, the composition containing a first alkoxysilyl perfluoropolyether adduct; (c) curing the first coating at a temperature and a relative humidity sufficient to promote hydrolysis of the alkoxysilyl perfluoropolyether adduct component; (d) optionally, modifying the surface of the cured first coating using the same or different surface modification means as was used in (a); (e) applying a second coating composition to the cured first coating to form a second coating thereover, the composition containing a second alkoxysilyl perfluoropolyether adduct; and (f) curing the second coating at a temperature and a relative humidity sufficient to promote hydrolysis of the second alkoxysilyl perfluoropolyether adduct.

Description

PROCESS FOR FORMING AN ANTI-FOULING COATING SYSTEM

CROSS REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit of priority of U.S. Provisional Patent Application Nos. 61/438,751 . filed February 2, 2011 ; and 61/480,475, filed April 29, 2011 , each of which is incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

[0002] The present invention relates to processes for forming anti-fouling coating systems based on alkosysilyl perfluoropolyether adducts, and to substrates prepared by such processes.

BACKGROUND OF THE INVENTION

[0003] The surfaces of many common devices and appliances are susceptible to staining with fingerprints, skin oil, perspiration, cosmetics, etc. where touch by skin is likely to occur. For example, optical filters and lenses, eyeglass lenses, mirrors, electronic displays such as television screens and displays for handheld devices, as well as stainless steel appliance surfaces, are easily stained with fingerprints and/or cosmetics when used. Once adhering, such stains are not easily removable.

[0004] While perfluoropolyether-containing compounds are known to exhibit water and oil repellency and lubricity due to their low surface energy, such materials typically do not readily form continuous, adherent coatings on other surfaces. Also known in the art are hybrids of perfluoropolyether-containing compounds with organo silane coupling agents. Such hybrid materials exhibit better adhesion to a variety of substrates. However, coatings based on these materials often do not meet the strict durability requirements for application to surfaces that are subjected to frequent handling and touch by skin.

[0005] Such surface durability typically is evaluated comparatively using a device that applies a constant pressure on a uniform surface area that cycles from side to side across the coated surface. Long term hydrophobic and oleophobic properties are evaluated by measuring water contact angle after various intervals to obtain the relationship with rubbing cycles, as is described in detail in the Examples herein below.

[0006] In addition to durability, anti-fouling coatings must not adversely affect the appearance (aesthetics) of the surface to which they are applied. For most applications, the anti-fouling coating must be transparent, impart no color, and have sufficient rheological properties to allow a uniform, continuous coating layer over the surface(s) to which it is applied.

SUMMARY OF THE INVENTION

[0007] The present invention is directed to a process for forming a durable anti-fouling coating system on a substrate comprising:

(a) modifying a surface of the substrate using a surface modification means;

(b) applying a first coating composition to at least a portion of the modified substrate surface to form a first coating thereover, the first coating composition comprising as a component a first alkoxysilyl perfluoropolyether adduct;

(c) curing the first coating at a temperature and a relative humidity sufficient to promote hydrolysis of the alkoxysilyl perfluoropolyether adduct component to form a cured first coating on the substrate;

(d) optionally, modifying the surface of the cured first coating using the same or different surface modification means as was used in (a);

(e) applying a second coating composition to at least a portion of the surface of the cured first coating to form a second coating thereover, the second coating composition comprising as a component a second alkoxysilyl perfluoropolyether adduct which is the same or different from that comprising the first coating

composition; and

(f) curing the second coating at a temperature and a relative humidity sufficient to promote hydrolysis of the second alkoxysilyl perfluoropolyether adduct component to form a durable anti-fouling coating system on the substrate.

[0008] Substrates coated using the process also are provided. DETAILED DESCRIPTION OF THE INVENTION

[0009] It is noted that, as used in this specification and the appended claims, the singular forms "a," "an," and "the" include plural referents unless expressly and unequivocally limited to one referent.

[0010] For the purposes of this specification, unless otherwise indicated, all numbers expressing quantities of ingredients, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term "about." Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.

[0011] All numerical ranges herein include all numerical values and ranges of all numerical values within the recited numerical ranges. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contain certain errors necessarily resulting from the standard deviation found in their respective testing measurements.

[0012] As previously mentioned, the present invention provides a process for forming a durable anti-fouling coating system on a substrate comprising:

(a) modifying a surface of the substrate using a surface modification means;

(d) optionally, modifying the surface of the cured first coating using the same or different surface modification means as was used in (a); (e) applying a second coating composition to at least a portion of the surface of the cured first coating to form a second coating thereover, the second coating composition comprising as a component a second alkoxysilyl perfluoropolyether adduct which is the same or different from that comprising the first coating

composition; and

SUBSTRATES:

[0013] Substrates suitable for coating by the process of the present invention can include any substrate that might encounter frequent handling, especially substrates that may come into contact with skin oils. Suitable substrates can include, but are not limited to metallic substrates, glass substrate and/or organic polymeric substrates.

[0014] Examples of suitable metallic substrates can include ferrous metals and non-ferrous metals. Suitable ferrous metals can include, but are not limited to iron, steel, and alloys thereof. Non-limiting examples of useful steel materials include cold-rolled steel, galvanized (zinc coated) steel, electrogalvanized steel, stainless steel, pickled steel, GAL VAN N E AL^®, GALVALUME^®, and GALVAN^® zinc- aluminum alloys coated upon steel, and combinations thereof. Useful non-ferrous metals include, but are not limited to aluminum, zinc, magnesium and alloys thereof. Combinations or composites of ferrous and non-ferrous metals can also be used. In a particular embodiment of the present invention, the substrate comprises stainless steel.

[0015] As used herein and in the appended claims, the term "glass" is defined as being an inorganic substance, e.g., an inorganic silicate. Glass substrates can be of any type suitable for the intended purpose; but generally are a clear, low colored, transparent glass such as the well-known silica type of glass, particularly soda-lime-silica glass. The nature and composition of various silica glasses are well known in the art. The glass can be a strengthened glass, e.g., strengthening by thermal or chemical tempering. [0016] Organic polymeric substrates that can be used in the process of the present invention are any of the currently known (or later discovered) plastic materials that are useful, for example, as optical substrates chosen from the art- recognized synthetic organic resins, e.g., organic optica! resins, that are used to prepare optically clear castings for optical applications, such as for display screens or as ophthalmic lenses. Non-limiting examples of organic polymeric substrates suitable for use in the process of the present invention are polymers, e.g., homopolymers and copolymers, prepared from the monomers and mixtures of monomers disclosed in U.S. Patent 5,962,617, and from column 15, line 28 to column 16, line 17 of U.S. Patent 5,658,501 , which disclosure is incorporated by reference. Such organic substrates can be thermoplastic or thermoset polymeric substrates. Such polymeric substrates can include, for example, thermoplastic polymers having a high glass transition temperature, and highly cross-linked polymers. Also, the organic polymeric substrates can be transparent substrates having a refractive index that ranges from 1.48 to 1.74. Alternatively, the organic polymeric substrate can have a refractive index ranging from 1 .54 to 1.56, or greater than .60, e.g., from 1 .60 to 1.74.

[0017] Suitable non-limiting specific examples of organic polymeric substrates can include those comprised of: polyol(allyl carbonate) monomers, e.g., allyl diglycof carbonates such as diethylene glycol bis(allyl carbonate), which monomer is sold under the trademark CR-39 by PPG Industries, Inc, and copolymers thereof; polyurea-polyurethane (polyurea urethane) polymers, which are prepared, for example, by the reaction of a polyurethane prepolymer and a diamine curing agent, a composition for one such polymer being sold under the trademark TRIVEX by PPG Industries, Inc; acrylic functional monomers, such as but not limited to, polyol(meth)acryloyl terminated carbonate monomers; diethylene glycol dimethacrylate monomer; ethoxylated phenol methacrylate monomers; diisopropenyl benzene monomer; ethoxylated trimethylol propane triacrylate monomers; ethylene glycol bismethacrylate monomer; poly(ethylene glycol) bismethacrylate monomers; urethane acrylate monomers; poly(ethoxylated bisphenol A dimethacrylate) monomers; polyvinyl acetate); poly(vinyl alcohol); poly(vinyl chloride); poly(vinylidene chloride); polyolefins, such as polyethylene and polypropylene; polyurethanes; polythiourethanes monomers, which include, but are not limited to materials such as the MR-6, MR-7, MR-8 and MR-10 optical resins sold by Mitsui Chemicals, Inc; thermoplastic polycarbonates, such as the thermoplastic bisphenol A-based polycarbonates, e.g., a carbonate-linked resin derived from bisphenol A and phosgene, one such material being sold under the trademark LEXAN; polyesters, such as the material sold under the trademark MYLAR; poly(ethylene terephthalate); polyvinyl butyral; poly(methyl methacrylate), such as the material sold under the trademark PLEXIGLAS, and polymers prepared by reacting polyfunctional isocyanate(s) with polythiol(s) or polyepisulfide monomers (such as the monomer sold under the trade name IU-10 by Mitsubishi Gas Chemicals, Inc.), either homopolymerized or co-and/or terpolymerized with polythiols, polyisocyanates, polyisothiocyanates and optionally ethylenically unsaturated monomers or halogenated aromatic-containing vinyl monomers.

SURFACE MODIFIERS:

[0018] In the process of the present invention, the surface of the substrate is modified using a "surface modification means" (i.e., a surface modifier). Effective surface modifiers can include treatments such as activated gas treatment, e.g., treatment with a low temperature plasma or corona discharge. Inert gases, such as argon, and reactive gases, such as oxygen, have been used as the plasma gas. Inert gases will roughen the surface, while reactive gases such as oxygen will both roughen and chemically alter slightly the surface exposed to the plasma, e.g., by producing hydroxyl or carboxyl units on the surface. Obviously, the extent of the surface roughening and/or chemical modification will be a function of the plasma gas and the operating conditions of the plasma unit (including the length of time of the treatment).

[0019] Additional surface modifiers can include, but are not limited to, ultrasonic washing, e.g., with an aqueous soap/detergent solution, cleaning with an aqueous mixture of organic solvent, e.g., a 50:50 mixture of isopropanol:water or ethanol:water, UV treatment, and chemical treatment that results in hydroxylation of the substrate surface, e.g., etching of the surface with a caustic solution such as an aqueous solution of alkali metal hydroxide, e.g., sodium or potassium hydroxide, or exposing the surface to a chemical vapor. With respect to glass substrates, suitable surface modification means also can include fluoride-containing glass-etchants that results in creation of free silicon-oxygen bonds on the glass surface. Such fluoride- containing glass etchants can include, e.g., hydrogen fluoride, hydrofluoric acid, ammonium fluoride, sodium fluoride, sodium bifluoride, potassium fluoride, potassium bifluoride, and/or ammonium hydrogen difluoride (ammonium bifluoride). For stainless steel substrates, ferric chloride can be a suitable etchant. The surface modification means also can include rubbing or wiping, for example with a cloth or brush.

[0020] After modifying the surface of the substrate, a first coating

composition is applied to at least a portion of the modified substrate surface to form a first coating thereover. The first coating composition comprises as a component a first alkoxysilyl perfluoropolyether adduct.

ALKOXYSILYL PERFLUOROPOLYETHER ADDUCTS

[0021] Many alkoxysilyl perfluropolyether materials are known and widely used. A wide variety of these materials are suitable for use in the first and second coating compositions used in the processes of the present invention. In a particular embodiment of the present invention, the alkoxysilyl perfluoropolyether adduct is selected from those having the following structural formulas I and/or II.

[0022] In Formula I, q is an integer from 1 to 3; m, n, and o are independently integers from 0 to 200; p is 1 or 2; X is O or a bivalent organic group; r is an integer from 2 to 20; R¹ is C_1-22 linear or branched hydrocarbon group; a is an integer from 0 to 2; and X' is a hydrolysable group. X' can be, for example, a hydrolysable group chosen from alkoxy groups, such as methoxy, ethoxy, propoxy and butoxy groups; alkoxyalkoxy groups, such as methoxymethoxy and methoxyethoxy; acyloxy such as acetoxy; alkenyloxy groups such as isopropenoxy; and halogen groups such as chloro, bromo and iodo.

[0023] In Formula II, q is an integer from 1 to 3; m, n, and o are independently integers from 0 to 200; p is 1 or 2, X is O or a bivalent organic group; r is an integer from 2 to 20; R¹ is a C_{1 -22} linear or branched hydrocarbon group; a is an integer from 0 to 2; X' is a hydrolysable group; and z is an integer from 0 to 10 when a is 0 or 1.

[0024] X' can be, for example, a hydrolysable group chosen from alkoxy groups, such as methoxy, ethoxy, propoxy and butoxy groups; alkooxyalkoxy groups, such as methoxymethoxy and methoxyethoxy; acyloxy such as acetoxy; alkenyloxy groups such as isopropenoxy; and halogen groups such as chloro, bromo and iodo.

[0025] Suitable alkoxysilyl perfluoropolyether adducts of the structural formulas I and II and the preparation thereof are described in detail in U.S. Published Patent Application No. 2009/0208728 at paragraphs [0030] to [0045], the cited portions of which are incorporated herein by reference.

[0026] Alternatively, alkoxysilyl perfluoropolyether adducts suitable for use in the present invention can include those represented by the following structural formula III.

[0027] In Formula III, Rf is a divalent straight-chain perfluoro polyether radical; R is C₁ to C₄ alkyl or phenyl; X is a hydrolysable group; n is an integer from 0 to 2; m is an integer from 1 to 5, and a is 2 or 3. In a particular embodiment, Rf is the divalent straight-chain perfluoro polyether radical having the structure:

-CF₂CF₂0(CF₂ CF₂ CF₂O)_kCF₂CF₂ - or

- CF₂(OC₂F₄)p (OCF₂)_q'- wherein k, p' and q' are each independently an integer of at least 1. Also X is a hydrolysable group chosen from alkoxy groups, such as methoxy, ethoxy, propoxy and butoxy groups; alkooxyalkoxy groups, such as methoxymethoxy and methoxyethoxy; acyloxy such as acetoxy; alkenyloxy groups such as isopropenoxy; and halogen groups such as chloro, bromo and iodo.

[0028] Suitable alkoxysilyl perfluoropolyether adducts of the structural formula III and the preparation thereof are described in detail in EP 1 300 433 B1 at paragraphs [0024] to [0034], the cited portions of which are incorporated herein by reference.

[0029] Mixtures of suitable alkoxysilyl perfluoropolyether adducts can be used in the first and second coating compositions used in the processes of the present invention. In a particular embodiment of the present invention, the first alkoxysilyl perfluoropolyether adduct is one represented by the structural formula I and/or II.

[0030] Typically the alkoxysilyl perfluoropolyether adduct is applied in the form of a solution of the adduct in an appropriate solvent. The solvent can include any of an number of known organic solvents provided that the organic solvent does not react with the alkoxysilyl perfluoropolyether adduct (or any other components present in the coating composition). Particularly suitable solvents can include fluorine-containing solvents such as a fluorine-containing alkane, a fluorine- containing haloalkane, a fluorine-containing aromatic, and a fluorine-containing ether, e.g., hydrofluoroether (HFE) such as Novec™ HFE 7100 or 7200 commercially available from 3M Company. Mixtures of appropriate solvents can be used.

[0031] The concentration of the alkoxysilyl perfluoropolyether adduct present in the first coating composition can range from 0.01 to 80 percent, such as 0.01 to 70 percent, or 0.05 to 60 percent, or 0.1 to 50 percent based on total weight of the first coating composition. The concentration of the alkoxysilyl perfluoropolyether adduct present in the first coating composition can range between any of these values inclusive of those recited.

[0032] The first coating composition can be applied to the surface modified substrate by any coating method known in the art. Suitable application methods can include, but are not limited to, wet coating methods and dry coating methods. Wet coating methods can include, for example, spray coating, spin coating, dip coating, flow coating, roll coating and like methods. Dry coating methods can include, for example, Physical Vapor Deposition, such as vacuum evaporation, reactive deposition, ion beam assisted deposition, sputtering, ion plating, and like methods; and Chemical Vapor Deposition.

[0033] After application of the first coating composition as described above, the first coating is cured at a temperature and a relative humidity sufficient to promote hydrolysis of the alkoxysilyl perfluoropolyether adduct component. Obviously, the cure time will be dependent upon the curing temperature and the relative humidity. For example, the first coating can be cured at a temperature of 25°C and a relative humidity of 40% for a period of 24 hours; or the first coating can be cured at a temperature of 60°C and a relative humidity of 80% for a period of 2 hours; or the first coating can be cured at a temperature of 130°C and a relative humidity of 60% for a period of 1 hour; or the first coating can be cured at a temperature of 130°C at a relative humidity of 80% for a period of 0.5 hour. In a particular embodiment of the present invention, the cure temperature can range from 20°C to 500°C, such as from 25°C to 350°C, or from 30°C to 250°C; and the relative humidity can range from 1 % to 99%, such as from 2% to 95%, or from 5% to 85%. The aforementioned temperature can range between any of the recited temperature values inclusive of the recited temperature values. Likewise, the aforementioned percent relative humidity can range between any of the recited relative humidity values, inclusive of the recited relative humidity values.

[0034] If desired, cure times may be reduced through the use of a hydrolytic condensation catalyst. Non-limiting examples of suitable such catalysts can include organic tin compounds (e.g., dibutyltin dimethoxide and dibutyltin dilaurate), organic titanium compounds (e.g., tetra-n-butyl titanate), organic acids (e.g., acetic acid and methanesulfonic acid), and mineral acids (e.g., hydrochloric acid, nitric acid, and sulfuric acid). When employed, the catalyst can be present in a catalytic amount in the first and/or second coating compositions used in the processes of the present invention. For example, the catalyst can be present in the first and/or second coating compositions in an amount ranging from 0.01 to 5 parts by weight, such as from 0.1 to 1 part by weight based on 00 parts of the alkoxysilyl perfluoropolyether adduct present in the first and/or second coating compositions. Alternatively, the catalyst may be present as a vapor during the curing, e.g., as a vapor of a solution of any of the aforementioned organic acids and/or the mineral acids.

[0035] In accordance with the process of the present invention, once the first coating composition is cured to form a cured coating on the surface of the substrate, the surface of the first coating, optionally, is modified using the same or different surface modification means as was used to surface modify the substrate. Any of the aforementioned surface modification means previously described above with respect to the substrate can be used provided the surface modification means does not remove or otherwise compromise the integrity of the first coating. In a particular embodiment of the present invention, the surface modification means used to treat the surface of the first coating results in hydroxylation of the first coating surface. After surface modification of the first cured coating (when a surface modification is used), or after cure of the first coating when surface modification of the first coating is not used, a second coating composition is applied to at least a portion of the modified surface of the cured first coating to form a second coating thereover. The second coating composition can be the same as or different from the first coating composition. The second coating composition comprises as a component a second alkoxysilyl perfluoropolyether adduct, which can be the same or different from that comprising the first coating composition. The second coating composition may be any of those compositions described above with respect to the first coating composition. The second coating composition may be identical to the first coating composition; or it may be different. Likewise, the second alkoxysilyl perfluoropolyether adduct used in the second coating composition can be the same as the first alkoxysilyl perfluoropolyether adduct, or it may be different. In a particular embodiment of the present invention, the second alkoxysilyl perfluoropolyether adduct is one represented by the structural formula I and/or II.

[0036] Any of the coating application techniques described above with respect to the first coating composition can be used to apply the second coating composition.

[0037] After application of the second coating composition to form a second coating over at least a portion of the first coating, the second coating is cured at a temperature and a relative humidity sufficient to promote hydrolysis of the second alkoxysilyl perfluoropolyether adduct component. Curing times, temperatures, and relative humidity for the second coating are as described above with respect to the first coating.

[0038] The process of the present invention provides an adherent, clear, and durable anti-fouling coating system on a variety of substrates. As previously mentioned, surface durability typically is evaluated comparatively using a device that applies a constant pressure on a uniform surface area that cycles from side to side across the coated surface. Long term hydrophobic and oleophobic properties are evaluated by measuring water contact angle after various intervals to obtain the relationship with rubbing cycles, as is described in detail in the examples herein below.

[0039] The present invention is more particularly described in the following examples, which are intended to be illustrative only, since numerous modifications and variations therein will be apparent to those skilled in the art.

EXAMPLES

Example

Part A - Preparation of Coating Solution A

Into a suitable container equipped with a mixer was added 199.0 grams (g) of HFE-7 00 3M™ Novec™ Engineered Fluid from 3M Company and 1 .0 g of Dow Corning® 2634 solution (now Dow Corning® 2700 solution) and mixed for 10 minutes.

Part B - Preparation of Substrates

Ten glass substrates measuring 5.5 mm by 1 1 .0 mm and ten stainless steel substrates measuring 6.0 mm by 10 mm were each immersed in a 12.5 weight percent sodium hydroxide aqueous solution in an ultrasonic bath maintained at 50°C for 5 minutes; sequentially rinsed in two ultrasonic baths containing deionized (Dl) water maintained at 50°C for 5 minutes in each bath; rinsed with Dl water and then with isopropyl alcohol; and dried for 10 minutes in a convection oven maintained at 60°C.

Part C - Coating of Substrates Coating Solution A (1.0 g) was dispensed over a period of 6 seconds onto each of the glass and stainless steel substrates while spinning for 11 seconds at a speed of 1 100 revolutions per minute on a Stir-Pak® spin coater (Cole-Parmer Instrument Company). The coated substrates were placed in a convection oven (20" x 20" size, VWR International, LLC), with the temperature set at 130°C for 30 minutes. Also in the oven were two wide mouth beakers (150 mm diameter and 75 mm in height) with ¾ of the volume of each filled with Dl water. After 30 min, the substrates were removed from the oven and left to cool to room temperature. The surface of each coated substrate was wiped with a soft cloth (AlphaWipe^® synthetic wipers).

Step 2

The coated stainless steel substrates were subjected to the process of Part B again. Step 3

Both the coated stainless steel substrates from Step 2 and the coated glass substrates from Step 1 were coated again following the procedure of Step 1.

Part D - Dl Water Contact Angle Testing

The Dl water contact angle was determined using a VCA 2500XE Video Contact Angle system (AST Products, Billerica, MA) according to the Operating Manual, VCA 2500 Video Contact Angle System User's Manual, March 17, 1997. Dl water (1.0 μΙ) was dispersed onto the coated substrates of Part C at three different locations. The left contact angle and right contact angle were read from each drop of Dl water simultaneously. The average Dl water contact was then calculated and reported in Table 1 herein below.

Part E - Permanent marker testing

A stainless steel substrate and a glass substrate were each coated with Coating Solution A following the steps of Parts B and C, except that EUROLENS^® Model 1400 lens saver tape was applied to about half of the surface of each substrate prior to Part C. The resulting substrates were marked with a Sharpie® King size™ permanent marker across both the coated and uncoated surfaces. A marker line of about 5 mm width was observed on the uncoated surfaces but on the coated side only beads of the marker ink were present. The beads were easily removed with the previously described soft cloth but the marker on the uncoated surface was not removable.

Whereas the present invention has been described with reference to specific details of particular embodiments thereof. It is not intended that such details be regarded as limitations upon the scope of the invention except insofar as and to the extent that they are included in the appended claims.

Claims

Therefore, we claim:

1 . A process for forming a durable anti-fouling coating system on a substrate comprising:

(a) modifying a surface of the substrate using a surface modification means;

(e) applying a second coating composition to at least a portion of the surface of the cured first coating to form a second coating thereover, the second coating composition comprising as a component a second alkoxysilyl perfluoropolyether adduct which is the same or different from that comprising the first coating composition; and

2. The process of claim 1 , wherein the substrate comprises metallic substrates, glass substrate and/or polymeric substrates.

3. The process of claim 1 , wherein the first coating composition and the second coating composition are the same composition.

4. The process of claim 1 , wherein the surface modification means is selected from surface rubbing, contacting with acidic solution, contacting with a fluoride containing etchant solution, contacting with a ferric chloride etchant solution, contacting with caustic solution, treating with plasma, treating with corona, exposing to UV radiation, ultrasonicating, and/or exposing to a vapor.

5. The process of claim 1 , wherein the surface modification means used in (a) and (d) are the same.

6. The process of claim 5, wherein the surface modification means is contacting with caustic solution and/or a ferric chloride etchant solution.

7. The process of claim 5, wherein the substrate is stainless steel.

8. The process of claim 1 , wherein the surface modification means in (a) and (d) are different.

9. The process of claim 8, wherein the substrate is glass.

10. The process of claim 9, wherein the surface modification means is contacting with caustic solution and/or a contacting a fluoride containing etchant solution.

1 1 . The process of claim 1 , wherein the alkoxysilyl perfluoropolyether adduct is selected from an adduct having the structure (I) or (II):

wherein in Formula I, q is an integer from 1 to 3; m, n, and o are independently integers from 0 to 200; p is 1 or 2; X is O or a bivalent organic group; r is an integer from 2 to 20; R is C-i-₂₂ linear or branched hydrocarbon group; a is an integer from 0 to 2; and X' is a hydrolysable group; and

wherein q is an integer from 1 to 3; m, n, and o are independently integers from 0 to 200; p is 1 or 2, X is O or a bivalent organic group; r is an integer from 2 to 20; R¹ is a Ci-22 linear or branched hydrocarbon group; a is an integer from 0 to 2; X' is a hydrolysable group; and z is an integer from 0 to 10 when a is 0 or 1 .

12. The process of claim 1 , wherein the alkoxysilyl perfluoropolyether adduct has the following structure (III}:

wherein Rf is a divalent straight-chain perfluoro polyether radical; R is C-i-4 alkyl or phenyl; X is a hydrolysable group; n is an integer from 0 to 2; m is an integer from 1 to 5, and a is 2 or 3.

13. The process of claim 1 1 , wherein Rf is a divalent straight chain perfluoro polyether radical having the structure:

wherein k, p' and q' are each independently an integer of at least 1.

14. The process of claim 1 , wherein the cure temperature ranges from 20°C to 500°C, and the relative humidity ranges from 99% to 1 %.

15. The process of claim 14, wherein the cure temperature ranges from 30°C to 250°C, and the relative humidity ranges from 85% to 5%.

16. The process of claim 1 , further comprising wiping the cured first coating of (c) prior to modifying the surface thereof in (d). 7. The process of claim 14, further comprising wiping the cured second coating of (f).

18. The process of claim 10, wherein the fluoride containing glass etchant solution comprises a fluoride containing etchant chosen from hydrogen fluoride, hydrofluoric acid, ammonium fluoride, sodium fluoride, sodium bifluoride, potassium fluoride, potassium bifluoride, and/or ammonium bifluoride. 9. A coated substrate prepared by the process of claim 1.