HYDROPHOBIC COATING AND METHOD

Cross Reference to Related Applications

tool] This application is a continuation-in-part of United States Patent

Application 1 1 /866,897, filed October 3, 2007, which claims priority from

United States Provisional Patent Application 60/849,233, filed October 3, 2006, which are hereby incorporated by reference.

Background

[002] Many polymer/plastic materials have desirable bulk properties such as low density, low cost, good strength, and ease of processing that have allowed them to become integral components of countless consumer goods and devices. However, many plastics that have ideal bulk properties for certain applications are lacking in their surface properties, such as, for example, abrasion resistance and wetting. As a result, it may be desirable to coat a polymer/plastic to modify its surface so that its favorable bulk properties can be exploited for various uses.

[003] In many instances, various devices are designed to prevent water from entering interior portions of the devices in order to maintain proper functionality. Manufacturers often design devices to be used in environments where water or other liquid materials may come into contact with the devices and components of the devices. Devices and device components may have various protective coverings to protect interior portions of the devices and components. Often, the protective covering is made from multiple parts, resulting in various seams and openings that may expose interior portions to damage from liquids. Many devices also require small openings or interstices in the protective cover in order to allow air or other gases to flow freely between the interior and exterior of the device while preventing liquids from passing through the cover. For example, a battery used in powering an electronic device may be susceptible to damage from moisture, and may nonetheless require an external source of oxygen to operate. Additionally, devices may contain a liquid material that is intended to be contained within the device for an extended time until the liquid is dispensed. An ink jet cartridge, for example, often contains a liquid ink solution that is contained within the cartridge for extended periods. Summary

[004] Effective hydrophobic coatings have been disclosed in United States Patent Application 1 1 /866,897, filed October 3, 2007. It has been found that on some surfaces, the effectiveness of the coating varies widely over the compositions disclosed.

[005] An aspect of the invention involves treating a surface with an adhesion promoting compound or first silane or having at least one silane functional group and at least one amine group. The surface formed by the first silane is then treated with a second silane.

[006] Another aspect of the invention is treatment of a surface with a plasma to add an increased number of carboxyl groups to the surface before treatment of the hydrolyzed first silane with the amine group. Without being limited by theory it is believed that the treatment of the surface with an appropriate plasma should create an increased number of carboxyl groups on the surface for binding to the first silane.

[007] Another aspect of the invention is a reaction product of a surface, a hydrolyzed first silane with an amine group and a second silane.

[008] Another aspect of the invention is an article of manufacture comprising an article of a surface, a hydrolyzed first silane with an amine group and a second silane.

[009] Devices that may be treated by the present invention are any devices that may benefit having hydrophobic surfaces. These include, but are not limited to,

(1 ) anti-wetting/anti-fogging optical surfaces such as windows, vehicle windshields, lenses, optical devices, computer/led screens, and the like

(2) all fibers and textiles and anything made thereof, including but not limited to: apparel and other textile articles such as water-resistant outerwear (coats, jackets, liners, pants, gloves, footwear, socks, hats), stain resistant clothing, clothing (formal, casual, work, medical, athletic), carpeting & rugs, zipper fasteners, rope/cordage, camping equipment (tents, footprints, sleeping bags, sleeping pads, rain flies, screens, backpacks, dry bags, canopies), filters, upholstery, medical gowns, bedding (sheets, pillows, comforters, blankets, pillow cases, mattress pads, mattress covers, mattresses), Geotextiles, water sport apparel (swimming suits, wet suits, dry suits, Personal Flotation Devices, skull caps, booties, gloves), protective wear (chemical suites, bullet proof vests, firefighting apparel, helmets), and covers (pool covers, awnings, boat covers, protective covers)

(3) water/snow sports and vehicle applications such as boat hulls, flotation devices, water and snow skis and boards

(4) surfaces exposed to weather that may benefit from water resistance such as building materials of any material, such as synthetic or natural polymers (vinyl, wood, etc.), metals, and the doors and exterior surfaces of vehicles, such as cars, trains, and airplane, particularly for watercraft, and aircraft. The coating may be useful on surfaces to mitigate accumulation of ice on aerodynamic or wing lifting surfaces and the like.

(5) electronic devices, including those that are routinely or may be accidentally exposed to water or humid conditions, such as hearing aids, cell phones, portable computers, audio and video devices, and cameras,

(6) insulating materials such as feathers, hollow polymeric fibers, closed and open celled foam.

[0010] In general, any device where a hydrophobic surface may be applicable is contemplated; including those listed in the Background, and other suitable devices, such as, for example, electronic equipment (both portable and nonportable devices), medical devices (such as tools, implants, diagnostic equipment, catheters), batteries, and fishing articles

(lures, lines).

[0011] Coating may be formed on portions of completed article assemblies, article sub-assemblies, individual articles, device components, and/or shell components. Coating may have a substantially consistent thickness respective to surface. Alternatively, coating may be applied to surface intermittently and/or in a specific pattern. Additionally, coating may be applied to surface only on desired portions of surface, such as, for example, portions of surface contacting or in close proximity to a seam, hole, interstice, or other opening defined in surface or adjacent to surface, or interior or exterior surface portions. Coating may comprise an ultra-thin transparent layer, enabling coating to be formed on surface with little to no impact on functionality or aesthetics of article.

[0012] Suitable substrate materials that may be treated include, for example, synthetic polymers, such as acrylics, nylons, polyesters, Kevlar™, Nomex™, polyolefins (polyethylenes, polypropylene, and other polyolefins), polycarbonates, polystyrenes, and copolymers of these with each other and with other monomers. Also included are blends of any of these materials in the same substrate, or composites of these materials with fibers or other materials, such as carbon fiber composites. Also contemplated are natural materials such as vegetable fibers or materials (e.g, cellulosic, ligninous, cotton, hemp), animal fibers or materials (e.g. wool, hair, silk, feather, leather), minerals, ceramics, metals. Suitable materials also include wood, paper, plaster, glass, silicon, composite materials, silicon-based materials, semiconducting materials, and insulating materials. The surfaces may be coated directly upon a substrate material, or upon another suitable coating or film that is applied over the substrate (such as transparent plastic films for windshields or opaque films for waterproof surfaces). The materials can be in any suitable form, such as fiber, yarn, bulk cloth, film, sheet, or bulk form. The coating can be applied in a batch or continuous process.

Plasma treatment of the substrate:

[0013] The substrate is plasma treated to remove organic contamination and increase the number density of reactive sites on the surface. The plasma treatment may be either an air plasma, oxygen plasma, or a carbon dioxide plasma or equivalent. [0014] The carbon dioxide plasma is intended to increase the number density of carboxyl, -COOH, groups on the surface. Advantageously, the carbon dioxide plasma may also increase the number of carbonyl (C=0) groups on the surface. This can be achieved by using a C0 ₂ plasma, a mixture of C0 ₂ and H ₂ 0, a mixture of C0 ₂ and H ₂ , a mixture of C0 ₂ and 0 ₂ or a mixture of C0 ₂ , H ₂ , 0 ₂ and H ₂ 0. The highest number density of -COOH groups is achieved by adjusting different variables such as plasma power which can be anywhere between 1 W-5000W, plasma treatment time, plasma treatment temperature which can be from -100°C-600°C and plasma gas pressure. Other materials that might add carboxyl groups to a surface during plasma treatment include carbon monoxide (CO), formic acid, acetic acid, trifluoroacetic acid, oxalic acid, oxalyl chloride, etc.

[0015] Oxygen and/or air plasmas may also introduce reactive functional

groups on polymer surfaces, including but not limited to, carboxyl and carbonyl groups.

[0016] The substrate may comprise any material or combination of materials suitable for deposition of a silane compound. Examples of materials suitable for forming substrate include the materials listed above.

[0017] A suitable substrate includes materials that can react with the plasma to form binding groups, such as carboxyl groups, on the surface.

[0018] With respect to carboxyl groups, without being bound to any theory, it is believed that superior properties derive from a high- or higher-density of carboxyl groups, or even carbonyl groups, covalently bound to the surface of the substrate. These carboxyl, or carbonyl groups may form covalent linkages with amine groups in the first silane, or may simply interact via acid-base interactions. This occurs from the acid/base interaction of carboxyl groups and amine groups, which forms a covalent bond upon thermally-induced dehydration. These covalent linkages firmly attach the first silane to the surface, which in turn presents a robust, and adherent coating and presents a dense surface of reactive groups for attachment of the second silane. Carbonyl groups may also react with amine groups, especially when either the carbonyl or amine group is on an aryl moiety.

[0019] The result is that coatings using first silanes with amine groups create coatings with excellent properties, as demonstrated by data shown in the examples. In addition, the data shows that the combination of a carboxyl- (or carbonyl-) group producing plasma treatment and use of amino-containing first silanes appears to have a synergistic effect in producing coatings with improved properties.

[0020] As described below, the second silane to be chosen is to apply a

hydrophobic property to the surface. An article that may require treatment of its entire or a part of its surface. Other second silanes that would impart other properties to the surface are also contemplated.

[0021] FIG. 1 illustrates an exemplary article 20 comprising a substrate 22 and a coating 26. Substrate 22 may comprise a surface 24. Coating 26 may comprise an adhesion promoting layer 28 and a hydrophobic layer 30.

Article 20 may comprise any suitable article or device having a surface portion. Examples of article 20 may include, without limitation, any of those listed above, and also include electronic devices, silicon wafers, silicon chips, ink jet cartridges, plastic films, batteries, battery contacts, rechargeable batteries, mesh coverings, ear pieces, and components of the foregoing. Article 20 may also comprise surfaces formed in any shape, size, texture, or configuration, including, for example, planar surfaces, curved surfaces, rough surfaces, smooth surfaces, and/or irregular surfaces. Additionally, article 20 may include various hearing aid devices, components, and/or accessories, including, for example, shell components, covers, in-the-ear domes (e.g., for open ear products), microphone covers (e.g., fabric mesh covers), volume controllers, switches, buttons, microphone ports, receiver ports, tubing, ear hooks, acoustic damping elements, battery doors, batteries, battery contacts, nozzles, DAI connectors, moisture and/or wax guards, face plate elements, ear molds (e.g., for standard ear molds and custom ear molds), and any other hearing aid device or component. [0022] FIG. 2 illustrates a textile article 83, comprising fibers 81 , and yarns 82. To impart a hydrophobic surface to this article, the article, whether woven, knit, or non-woven, may be treated, or either the fibers or the yarns may be treated before manufacture of the woven, knit, or non- woven article.

[0023] FIG. 3 shows an exemplary portable electronic device (cell phone).

Hydrophobic surfaces may be applied to, for example, to casing 1 , front case 1 1 , rear case 12 , display screen 13, or keys 14, 15. Coatings may be selectively applied near the joints between 1 1 and 12, near holes and openings in the case, such as near openings for keys 14, 15. Other portable electronic devices, such as, PDAs, music players, media recorders and players, portable computers, and the like.

Optional Hydration of the substrate

[0024] Optionally the plasma treated substrate can be hydrated with water vapor to further increase the bonding with the First Silane. Optionally, the substrate may also be hydrated with water vapor prior to deposition of the first silane.

Deposition of First Silane:

[0025] The surface of the plasma-cleaned substrate is exposed to an amino silane, which is a silane with at least one amine group. The first or amino silane acts as an adhesion promoter for second silane. This silane could be any silane having an amine group. This amine group could be on an alkyl or aryl moiety. The substrate surface is exposed to the amino silane by any suitable system, such as vapor deposition systems.

[0026] In an aspect the first silane has at least one silane group. In an

exemplary embodiment, the silane group on the first silane may be represented by formula (I):

where R ¹ , R ² , and R ³ may each be, independently, F, CI, Br, I, H, OH, a methoxy group, an ethoxy group, an isopropoxy group, an alkoxy group, an acetoxy group, a methyl group, an alkyl group, an aryl group, a perfluoroalkyl group, a partially fluorinated alkyl group, a dimethylamino group, a dialkylamino group, an ethylamino group, a monoalkylamino group, an amino group, a phenyl group, or a methoxyethoxyethoxy group. The other group on the silane, which is not R ¹ , R ² , or R ³ , and is directed to the left of the silicon, could be any chemical moiety that gives desired amino functionality to the silane molecule.

[0027] In an aspect, first silane may be represented by formula (II):

where X is an amino group. In formula (II), n may be an integer from 0- 32. In additional embodiments, n may be an integer from 1 -18. In at least one embodiment, n may be an integer from 3-4. Additionally, in formula (II), R ¹ , R ² , and R ³ may be as defined above for formula (I).

[0028] In certain embodiments, the first silane may also be represented as

formula (III):

where L is any suitable group to attach the amine(s) and the silane(s). L may be branched or straight, alkyl or aryl, and p and m may independently be 1 or greater than 1 . There may also be more than one amine group in the molecule, where these amine groups may be primary, secondary, or tertiary. R , R ² , and R ³ may be as defined above for formula (I).

[0029] A suitable first silane is any compound that has amine groups that may interact with any surface carboxyl or carbonyl groups or other amine- reactive groups, and will interact favorably with the second silane. The L group may be any suitable group that does not interact or interfere with the attachment to the substrate or the second silane, or materially affect the properties of the surface, such as through chemical reactions, stereo interference, or the like. Suitable L groups, one or a combination of straight or branched carbon chains, optionally containing all kinds of possible atoms.

[0030] Examples of the first silane include, but are not limited to 4- aminobutyltriethoxysilane, 1 -amino-2-(dimethylethoxysilyl)propane, n- (2-aminoethyl)-3 -aminoisobutyldimethylmethoxysilane, n-(2-aminoctyl)-

3-aminoisobutylmethyldimethoxysilane,

(aminoethylaminomethyl)phenethyltrimethoxysilane,n-(2-aminoe thyl)-3- aminopropylmethyldimethoxysilane, n-(2-aminoethyl)-3

-aminopropyltriethoxysilane, n-(2-aminoethyl)-3- aminopropyltrimethoxysilane,n-(6-aminohexyl)aminopropyl- trimethoxysilane,n-(2-aminoethyl)-1 1 -aminoundecyltrimethoxysilane, 3-

(m-aminophenoxy)propyltrimethoxysilane, m- aminophenyltrimethoxysilane, p-aminophenyltrimethoxysilane, n-3-

[(amino(polypropylenoxy)]aminopropytrimethoxysilane, 3- aminopropyldiisopropylethoxysilane, 3- aminopropylmethylbis(trimethylsiloxy)silane, 3- aminopropyldimethylethoxysilane, 3-aminopropylmethyldiethoxysilane,

3-aminopropylpentamethyldisiloxane, 3- aminopropyltris(methoxyethoxyethoxy)silane, 3- aminopropyltris(trimethylsiloxy)silane, 1 1 -aminoundecyltriehoxysilane, 3- aminopropyltrimethoxysilane and 3-aminopropyltriethoxysilane. Hydrolysis:

[0031] The surface treated with the first silane is exposed to water vapors to hydrolyze -Si(OR) ₃ groups, or other hydrolyzable groups such as Si-CI, of the attached amino silane to -Si(OH) ₃ groups, which makes the surface more reactive towards the second silane.

[0032] The hydrolysis may be by any suitable system, such as exposing the surface to moisture.

Deposition of second silane:

[0033] After exposure to water vapors, the surface is treated with a second silane to impart a surface with desired properties. The second silane may be any second silane as disclosed in United States Patent

Application 1 1 /866,897.

[0034] A second silane is deposited upon and bonded to the adhesion

promoting layer. The second silane is often chosen to provide an outer layer with a hydrophobic surface. The second silane may also be chosen to provide other properties to the surface, such an oleophobic surface or a hydrophobic/oleophobic surface, or even a hydrophilic surface. As an example, the hydrophobic layer may comprise a second silane having at least one perfluorinated aliphatic group. The

hydrophobic layer may also comprise additional compounds in addition to the second silane. The additional compounds in hydrophobic layer may impart various desirable properties to hydrophobic layer, such as, for example, microbial resistance, without preventing the hydrophobicity of the hydrophobic layer and/or the second silane from acting as a hydrophobic and/or oleophobic layer or compound.

[0035] In order to impart hydrophobic characteristics to the coating, the second silane may comprise long alkyl chains, partially fluorinated alkyl chains, and/or alkyl chains that have regions that are perfluorinated, any of which may be straight or branched. The second silane may contain aryl groups. For example, the second silane may comprise alkyl chains having the general formulas CF ₃ (CF2)n(CH ₂ )mSiR R ² R ³ and/or

CF ₂ H(CF ₂ ) _n (CH ₂ ) _m SiR R ² R ³ , where n and m are integers (n greater than or equal to 0, and m greater than or equal to 0). In addition, the second silane and/or the hydrophobic layer may comprise mixtures of alkyl, perfluoroalkyl, or partially fluorinated alkyl chains.

[0036] The second silane may be capable of bonding to the first silane through, for example, a siloxane (Si-O-Si) linkage. Additionally, the second silane may be capable of forming polymers containing siloxane linkages. In an exemplary embodiment, the silane group on the second silane may be represented by formula (III):

where R ⁴ , R ⁵ , and R ⁶ may each be, independently, F, CI, Br, I, H, OH, a methoxy group, an ethoxy group, an isopropoxy group, an alkoxy group, an acetoxy group, a methyl group, an alkyl group, a perfluoroalkyl group, a partially fluorinated alkyl group, a dimethylamino group, a dialkylamino group, an ethylamino group, a monoalkylamino group, an amino group, a phenyl group, or a methoxyethoxyethoxy group.

[0037] In at least one embodiment, the second silane may be represented by formula (IV):

where n may be an integer from 0-32, and R ⁴ , R ⁵ , and R ⁶ may be as defined above for formula (III). In additional embodiments, n may be integer from 1 -16. In at least one embodiment, n may be an integer from 5-9.

Representative examples of the second silane include, without limitation, (tridecafluoro-1 ,1 ,2,2-tetrahydrooctyl)trichlorosilane, (tridecafluoro- 1 ,1 ,2,2-tetrahydrooctyl)methyldichlorosilane, (tridecafluoro-1 ,1 ,2,2- tetrahydrooctyl)trimethoxysilane, (tridecafluoro-1 ,1 ,2,2- tetrahydrooctyl)triethoxysilane, (tris(tridecafluoro 1 ,1 ,2,2- tetrahydrooctyl)dimethylsiloxy)chlorosilane, (heptadecafluoro-1 ,1 ,2,2- tetrahydrodecyl)trichlorosilane, triethoxy(1 H,1 H,2H,2H- perfluorooctyl)silane, (heptadecafluoro-1 ,1 ,2,2- tetrahydrodecyl)triethoxysilane, (heptadecafluoro-1 ,1 ,2,2- tetrahydrodecyl)trimethoxysilane, (heptadecafluoro-1 ,1 ,2,2- tetrahydrodecyl)methyldichlorosilane, (heptadecafluoro-1 ,1 ,2,2- tetrahydrodecyl)dimethylchlorosilane, perfluorododecyl-1 H,1 H,2H,2H- triethoxysilane-perfluorotetradecyl-1 H,1 H,2H- ,2H-triethoxysilane mixture, 1 ,8-bis(trichlorosilylethyl)hexadecylfluorooctane, n- octadecyldimethylchlorosilane, n-octadecyldimethylmethoxysilane, n- octadecylmethoxydichlorosilane, n-octadecylmethyldichlorosilane, n- octadecylmethoxydichlorosilane, n-octadecylmethyldiethoxysilane, n- octadecyltrichlorosilane, n-octadecyltriethoxysilane, n- octadecyltrimethoxysilane, n-octadecyldimethyl(dimethylamino)silane, n- triacontyldimethylchlorosilane, n-triacontyltrichlorosilane, n- hexadecyltrichlorosilane, n-hexadecyltrimethoxysilane, n- hexadecyltriethoxysilane, n-dodecyltrichlorosilane, n- dodecyltrimethoxysilane, n-dodecyltriethoxysilane, n- dodecylmethyldichlorosilane, n-octyltrichlorosilane, n- octyltrimethoxysilane, n-octyltriethoxysilane, n-octylmethyldichlorosilane, and n-octyldimethylchliorosilane. The second silane may also include compounds according to the general formula CH ₃ (CH2)nCHRCH ₂ SiCl3, where R = CH ₃ (CH ₂ )m, and n and m are integers (n greater than or equal to 0, and m equal to or greater than 0). The second silane may also include compounds according to the general formula

CH ₃ (CH ₂ )nCHRSiCI ₃ , where R = CH ₃ (CH ₂ ) _m , and n and m are integers (n greater than or equal to 0, and m greater than or equal to 0). The second silane may also include compounds according to the general formula CH ₃ (CH ₂ )nCHRSi(OCH ₃ )3, where R = CH ₃ (CH ₂ ) _m , and n and m are integers (n greater than or equal to 0, and m greater than or equal to 0).

[0039] In certain embodiments, the adhesion promoting layer and the

hydrophobic layer may comprise a germanium compound (e.g., a germane) in addition to or in place of a silane compound. Germanium compounds may function as adhesion promoting and hydrophobic compositions in a manner similar to analogous silicon compounds.

Accordingly, silicon compounds listed above as examples of the first silane or the second silane may be substituted with analogous

germanium compounds, in which the Si atom is replaced with a Ge atom.

[0040] A mixture of silanes could be employed in the second silane deposition.

For example, a silane with a perfluorinated tail and a silane containing an alkyl chain could be jointly deposited in this manner.

Use of a cross-linker:

[0041] The abrasion resistance of the coating can be further improved by using a cross-linker.

[0042] This cross-linker can be used in the following ways:

1 ) Deposition of a mixture of the cross-linker and the first amino silane;

2) Deposition of the cross-linker after deposition of the amino silane;

3) Deposition of a mixture of a cross-linker and an second silane;

4) Deposition of the cross-linker after deposition of the second silane.

[0043] The mixtures of the amino silane and cross-linker, and second silane and cross-linker may have any percentage of cross-linker in them. The use of this reagent will cross-link deposited aminosilane and/or second silane coatings, which will make them even more robust and hence more abrasion resistant. A variety of cross-linkers can be used for this purpose, e.g., diisocyantes, which have a general formula OCN-R-NCO, diacidchlorides, which have a general formula CIOC-R-COCI, diesters, e.g., dimethyl and diethyl esters, which have a general formula CH3COO-R-COOCH3 or C ₂ H ₅ COO-R-COOC ₂ H ₅ , where R is a carbon chain containing all kinds of possible atoms in it. Silanes can also be used as a cross-linker. These silanes have a general formula (RO) ₃ -Si- L-Si(OR) ₃ , (RO) ₂ CH ₃ -Si-L-Si-CH ₃ (OR) ₂ or RO(CH ₃ ) ₂ -Si-L-Si-(CH ₃ ) ₂ -OR _! where R may be C ₂ H ₅ , CH ₃ and L may be a carbon chain, such as an alkyl or aryl group, containing all kinds of possible atoms in it. Instead of alkoxy groups (-OR), one might also use chloro or acetoxy reactive groups on the silanes, or any other silane with a suitable reactive functional group. Other examples of possible cross-linkers are glycidoxypropyltrimethoxysilane and glutaraldehyde.

Brief Description of Drawings

[0044] FIG. 1 is a schematic cross-section of the coated article.

[0045] FIG. 2 a schematic view of a coated article.

[0046] FIG. 3 a schematic view of a coated article.

[0047] FIG. 4 is a chart showing wetting test parameters for determining water repellancy.

[0048] FIG. 5 is a chart use for determining standard spray test ratings.

[0049] FIG. 6 is a graph showing wetting test data.

Detailed Description Examples

[0050] The following procedure was essentially adhered to in the Examples that follow:

[0051] The applicability of the process was demonstrated by coating a nylon and polyester fabric. The process was done in a commercially-available plasma system: the chemical vapor deposition system YES-1224P from

Yield Engineering Systems, California. The entire process was done at 100°C and involved the following steps:

Plasma Cleaning/Treatment of Nylon and Polyester Substrate

[0052] The plasma cleaning/treatment of the substrate was performed in a CO ₂ or oxygen plasma. A total of four plates (two active plates and two ground plates) were employed, and the voltage was applied to the active plates for plasma generation. These plates were arranged in the order: active, ground, ground and active (AGGA) from top to bottom. The fabric was placed on the third plate from the top (the lower ground plate). The fabric was plasma treated at 100W for 2.5 minutes. Deposition of First Silane

[0053] After the plasma treatment, 1 mL of 3-aminopropyltrimethoxysilane was injected into the chamber. A reaction/surface adsorption was allowed to take place for 20 minutes. After the reaction, the unreacted silane was pumped out of the chamber. Hydrolysis of Amino-silane functionalized Nylon and Polyester

Substrates

[0054] Amino silane functionalized fabric was then exposed to water vapors by injecting 1 mL of water into the chamber. This hydrolysis was for 20 minutes. This treatment is believed to hydrolyze -Si(OR) ₃ groups of the amino silane to -Si(OH) ₃ groups, and hence make the surface more reactive towards the attachment of second silane. After the reaction, unreacted water was pumped out of the chamber.

Deposition of the Second Silane

[0055] In the final step, 1 mL of (tridecafluoro-1 ,1 ,2,2- tetrahydrooctyl)trimethoxysilane was injected into the chamber. This deposition was for 20 minutes. The unreacted silane was pumped out of the chamber after the reaction,

loose] Comparative tests were run using a C0 ₂ plasma, an 0 ₂ plasma, or an air plasma, and using an amine terminated first silane and a first

silane/adhesion promoter that is not amine terminated.

Example I

[0057] A comparative test was conducted which involves the use of 3- isocyanatopropyl triethoxysilane as the first silane or adhesion promoter in the treatment of a nylon surface. The process used an air plasma to oxidize the surface. The second silane, (tridecafluoro-1 ,1 ,2,2- tetrahydrooctyl)trimethoxysilane, was bonded to the first silane in an attempt to make the surface hydrophobic. However it was found the surface did not become hydrophobic after the deposition. In another comparative experiment, chemical vapor deposition was performed on nylon without using the isocyanato silane adhesion promoter, where the remaining process was the same. The surface did not become

hydrophobic. It was observed that (tridecafluoro-1 ,1 ,2,2- tetrahydrooctyl)trimethoxysilane does not adhere well to the nylon surface. The process was also applied to a polyethylene substrate and it was observed that the surface did not become hydrophobic. In summary, whether with or without the isocyanato adhesion promotion agent, the air plasma treated surface did not become hydrophobic when treated with the hydrophobic silane ((tridecafluoro-1 ,1 ,2,2- tetrahydrooctyl)trimethoxysilane).

Example 2

[0058] In the next set of experiments an amine-terminated first silane, 3- aminopropyl trimethoxy silane (APTMS) or 3- aminopropyl

triethoxysilane (APTES), was used as an adhesion promoter instead of 3-isocyanatopropyl triethoxysilane used in Example 1 . Use of either of these two amine terminated silanes resulted in nylon and polyethylene that were super hydrophobic. It was found that APTES and APTMS adhered well to all the surfaces tested, i.e., use of these silanes as the adhesion promoter in the process makes the surface hydrophobic.

Example 3

[0059] A nylon swatch having a hydrophobic coating was made by the same chemical vapor deposition (CVD) process as in Example 2, but using an oxygen plasma. The first and second silanes were APTMS, and

(tridecafluoro-1 ,1 ,2,2-tetrahydrooctyl)trimethoxysilane, respectively. The coated surfaces were tested for abrasion resistance by employing the following standard: ASTM D4966-98 (Martindale abrasion tester.) The coating came off the surface in less than 100 cycles. Example 4

[0060] The process of Example 3 was repeated, but the oxygen plasma was replaced with carbon dioxide plasma. The hydrophobic coating lasted at least 1700 cycles in the abrasion test. From this it can be concluded that use of a carbon dioxide plasma helped significantly improve the abrasion resistance of the coating as noted above in similar samples.

[0061]

Example 5

[0062] An Apple iPod was also coated using the process of Example 4. CVD was done at 60 °C. The process used a C0 ₂ plasma, APTMS was the adhesion promoter. Treatment by the plasma and application of the APTMS, was followed by hydrolysis and application of (tridecafluoro- 1 ,1 ,2,2-tetrahydrooctyl)trimethoxysilane. To test hydrophobicity, water contact angles were measured. Water contact angles may be used as a measure of surface hydrophobicity. A higher water contact angle for a surface may indicate that the surface has a higher degree of

hydrophobicity.

[0063] The water contact angles of the front (screen) and back (body) were 1 17±2 degrees and 1 13±7 degrees. Example 6

[0064] A comparative set of tests were conducted, comparing carbon dioxide plasma with oxygen plasma treatment, and comparing 3- aminopropyltrimethoxysilane (APTMS) and 3- isocyanatopropyltriethoxysilane (ICPTES) for the first silane. Samples were produced by treating pieces of polyester fabric as a substrate essentially as described above. All tests were done with 20 minute depositions of each silane, and a 20 minute hydrolysis step. The temperature of the reaction was 100°C.

[0065] To test hydrophobicity of the samples, wetting tests similar to the Dupont Water Drop Test LS & CO Method 42 were conducted with

water/isopropylalcohol (I PA) mixtures. For example, 98/2 means a mixture of 98% water and 2% I PA. The results of the test are shown in Table 1 . See FIG. 4 for a description of test results listed. (In short, a score of "4" means passing, a score of "1 " represents complete failure.)

[0066] In addition, water spray tests were performed in accordance with the

AATCC Test Method 22-2005, Water Repellency: Spray Test. The spray 5 patterns were evaluated by comparison to a rating chart, which is shown in FIG. 5, and with reference to Table 2. The results are shown in Table 1 .

Table 1

Initial Wetting and Spray Tests After Treatment

WetWetWetWetWetWetWetWetWetting ting ting ting ting ting ting ting ting test test test test test test test test test Spray

Sample 100/0 98/2 95/5 90/10 80/20 70/30 60/40 50/50 40/60 Test

C0 ₂ /APTMS 4 4 4 4 4 4 4 3.5 2 100

0 ₂ /APTMS 4 4 4 4 4 4 3.7 3 1 100

C0 ₂ /ICPTES 4 2 1 1 1 1 1 1 1 60

0 ₂ /ICPTES 4 3 2 1 1 1 1 1 1 65

10 Table 2

Spray Test Evaluation

Rating Evaluation

100 No sticking or wetting of upper surface

90 Slight random sticking or wetting of upper surface

80 Wetting of upper surface at spray points

70 Partial wetting of whole of upper surface

50 Complete wetting of whole of upper surface

0 Complete wetting of whole upper and lower surfaces

[0067] With reference to Table 1 , in instances where APTMS was used, there is a marked improvement in hydrophobicity as indicated by the wetting tests and the spray tests. Comparing the oxygen/ICPTES data with the carbon dioxide/ICPTES data there is small decrease in hydrophobicity when carbon dioxide plasma treatment is used, which may suggest that the oxygen plasma leads to the introduction of more -OH groups on the plasma treated surface while the carbon dioxide plasma leads to the introduction of more carboxyl groups on the plasma treated surface.

[0068] For the carbon dioxide plasma treatment, there is a marked degradation when ICPTES is used as the first silane. Unexpectedly, when the carbon dioxide plasma was used with the APTMS first silane there was a marked improvement, as shown by both the wetting test results and the spray test results. This indicates that there may be a synergistic interaction between the carbon dioxide treated surface and the first silane APTMS as it bonds to the surface. Example 7

[0069] Samples of polyester cloth were prepared and treated essentially as above with C0 ₂ plasma and 0 ₂ plasma using APTMS as the first silane. A washing test was accomplished by sewing the samples to a larger cloth and washing the cloth several times in a standard washing machine. Along with this sample of cloth, ballast materials were present in the washing machine to simulate a wash in a real washing machine cycle, similar to AATCC "Standardization of Home Laundry Test Conditions." After a set number of wash cycles the samples were tested with the wetting test and spray test as described in Example 6. The data collected is located below in Table 3.

Table 3

Samples v. Washing

WetWetWetWetWetWetWetWet¬

# of ting ting ting ting ting ting ting ting

WAS test test test test test test test test Spray

Sample HES 98/2 95/5 90/10 80/20 70/30 60/40 50/50 40/60 Test

C0 ₂ /APTMS 0 4 4 4 4 4 4 3.5 2 100

C0 ₂ /APTMS 1 4 4 4 4 4 2.7 1 1 100

C0 ₂ /APTMS 5 4 4 4 4 2 1 1 1 90

C0 ₂ /APTMS 10 4 4 4 4 1 1 1 1 85

C0 ₂ /APTMS 15 4 4 4 4 1 1 1 1 85

C0 ₂ /APTMS 20 4 4 4 2 1 1 1 1 80

C0 ₂ /APTMS 25 4 4 4 1 1 1 1 1 75

0 ₂ /APTMS 0 4 4 4 4 4 3.7 3 1 100

0 ₂ /APTMS 1 4 4 4 4 3.3 1 1 1 100

0 ₂ /APTMS 5 4 4 4 4 1 1 1 1 95

0 ₂ /APTMS 10 4 4 4 2 1 1 1 1 85

0 ₂ /APTMS 15 4 4 4 3.7 1 1 1 1 85

0 ₂ /APTMS 20 4 4 4 2 1 1 1 1 80

0 ₂ /APTMS 25 4 4 4 1 1 1 1 1 80

[0070] As shown by data contained in Table 1 and Table 3 above, the 5 C0 ₂ /APTMS and 0 ₂ /APTMS samples show superior hydrophobicity and durability as compared to the C0 ₂ /ICPTES and 0 ₂ /ICPTES samples.

[0071] In FIG. 6 is a graphical representation of data the wetting test data contained in Table 3 above.

Example 8

10 [0072] All samples described in Example 6 and Example 7 above were

subjected to a Martindale Abrasion Test following standard ASTM D4966-98. The results are listed below in Table 4.

Table 4

Treated Samples vs Martindale Abrasion Test

15

Description: Water was used to test the hydrophobicity of the surfaces

^* 90/10 (H ₂ O/IPA) solution does not wet the surfaces even after 5000 abrasion cycles [0073] As these results indicate, the combinations of 02/APTMS and

C02/APTMS performed significantly better when subjected to the Martindale Abrasion Test.

[0074] While this invention has been described with reference to certain

specific embodiments and examples, it will be recognized by those skilled in the art that many variations are possible without departing from the scope and spirit of this invention, and that the invention, as described by the claims, is intended to cover all changes and

modifications of the invention which do not depart from the spirit of the invention.