Zhang, Hua (1/1 Templeman Crescent, Hillsdale, NSW 2036, AU)
Raston, Colin Llewellyn (18 Leumear Street, East Oakleigh, VIC 3168, AU)
Lamb, Robert Norman (9 Gamut Road, Engadine, NSW 2233, AU)
Zhang, Hua (1/1 Templeman Crescent, Hillsdale, NSW 2036, AU)
Raston, Colin Llewellyn (18 Leumear Street, East Oakleigh, VIC 3168, AU)
DERWENT ABSTRACT, Accession No. 95-012038/02, Class A82, G02, (A14) XP002958094 & JP,A,06 299 088 (MITSUBISHI RAYON CO. LTD.) 25 October 1994.
See also references of EP 0969934A1
|1.||A method of applying an hydrophobic film to a surface, the method comprising the steps of: (a) optionally niodifying particles to be coated on the surface so as to for functional groups thereon; (b) applying particles having functional groups thereon to the surface to be coated; and (c) treating the applied particles such that the particles are bound together and to the surface by chemical crosslinking of the functional groups on the particles.|
|2.||A method of applying an hydrophobic film to a surface, the method comprising the steps of: (a) optionally modifying particles to be coated on the surface so as to for functional groups thereon; (b) mixing particles having functional groups thereon with a nonsilicone polymer reactive to the functional groups on the particles; (c) applying the mixture of particles and the nonsilicone polymer to the surface to be coated; and (d) treating the applied particles and nonsilicone polymer such that the particles are bound together and to the surface by chenbcal crosslinking of the functional groups on the particles.|
|3.||The method according to claim 2 wherein the nonsilicone polymer is polyurethane.|
|4.||The method according to claim 3 wherein the polyurethane is fouled by the reaction of di or polyisocyans with polyols.|
|5.||The method according to claim 4 wherein the polyurethane is formed by the reaction of methylene bis(phenyl isocyanate) (MDI) with polydinlethylsiloxane (PDMS) with hydroxyl groups terminated or 2,2,3,3,4,4,5 .5octafluoro1,6hexanediol.|
|6.||The lllethod according to any one of claims 1 to 5 wherein the particles are selected from the group consisting of silica particles. and metal oxides.|
|7.||The method according to claim 6 wherein the particles are silica particles.|
|8.||The method according to claim 6 wherein the metal oxide is titanium dioxide.|
|9.||The method according to any one of claims 6 to 8 wherein the particles have a diameter of between 20 to 100 nm.|
|10.||The method according to claim 7 wherein the optional modifying step (a) involves generating silylalkylmethacrylate groups such as silylpropylmethalcrylate (or related) functional groups, or a mixture of those funcilonal groups and passive silylalkyl groups on the silica particles.|
|11.||The method according to claim 10 wherein the chemical crosslinking of the functional groups on the silica particles is achieved by the addition of a copolynlerisation monomer, such as styrene, to link methacrylate functional groups from one particle to methacrylate functional groups on another particle.|
|12.||The method according to any one of clams 1 to 11 wherein the cross linking is activated photolytically by nleans of ultraviolet radiation or by using a radical initiator such as benzoyl peroxide or diethoxyacetophenol.|
|13.||The method according to any one of claims 1 to 12 wherein the particles and the polymer, if used, are applied to the surface in a slurry.|
|14.||The method according to claim 13 wherein the slurry is in an organic solvent.|
|15.||The method according to claim 14 wherein the solvent is selected from the group consisting of hexane, toluene, and ethyl acetate.|
|16.||The lllethod according to any one of claims 1 to 15 wherein the coated surface has a contact angle of water of at least 1500, preferably at least 1600. and more preferably about 165°.|
|17.||An object having at least a portion of its surface coated with a hydrophobic film applied by the method according to any one of claims 1 to 16.|
|18.||Use of the method according to any one of claims 1 to 16 to coat at least part of the surface of an object.|
Background Art It is well understood that the wettability of various lllaterials is dependent on both the physical and chemical heterogeneity of the material.
The notion of using the contact angle û nmde by a droplet of liquid on a surface of a solid as a quantitative llleasure of the wetting ability of the particular solid has also long been well understood. If the liquid spreads completely across a surface and forms a fill. the contact angle 0 is 00. If there is any degree of beading of the liquid on the surface of the solid, the surface is considered non-wetting.
For water, where the contact angle is greater than 0°, the solid is considered hydrophobic. Examples of materials on which liquid droplets have high contact angles, include water on paraffin which has a contact angle of about 107° and mercury on soda-lime glass which has a contact angle of about 140°.
In the past, surfaces have been protected against encrustation. corrosion, icing and fouling by means of coatings containing polymer films, hydrophobic solid fillers and hydrophobic liquids. One disadvantage of the use of such coatings is that they do not achieve multi-purpose protection since they are not generally versatile enough to protect against drainage fro a variety of causes.
International Application No WO 94/09074 discloses a multi-purpose solid surface modifier which comprises a composition containing a highly dispersed hydrophobic powder, a silicone liquid, a solvent. and an adhesive for binding the powder together and to the surface. The modifier is described as being effective in inparting water repellent, anti-fouling, anti-icing, anti- corrosive and anti-friction properties to various surfaces. Although the
specification describes exceptionally good experimental results, allegedly providing contact angles in some cases in excess of 175°, in practice it is very difficult to accurately measure contact angle data in excess of 165".
The present inventors have now developed methods of producing hydrophobic films that are an improvennt over the prior art methods. The present invention arises in part from the realisation that the hydrophobicity of a surface coating is determined by two factors, the first being the chemical properties of the material making up the hydrophobic coating or film, and the second being the physical surface conditions.
Disclosure of Invention In a first aspect, the present invention consists in a method of applying an hydrophobic film to a surface, the method comprising the steps of: (a) optionally modifying particles to be coated on the surface so as to for functional groups thereon; (b) applying particles having functional groups thereon to the surface to be coated; and (c) treating the applied particles such that the particles are bound together and to the surface by chemical cross-linking of the functional groups on the particles.
In a second aspect, the present invention consists in a method of applying an hydrophobic film to a surface, the method comprising the steps of: (a) optionally modifying particles to be coated on the surface so as to fonn functional groups thereon; (b) mixing particles having functional groups thereon with a non-silicone polymer reactive to the functional groups on the particles; (c) applying the mixture of particles and the non-silicone polymer to the surface to be coated; and (d) treating the applied particles and non-silicone polymer such that the particles are bound together and to the surface by chemical cross-linking of the flinctional groups on the particles.
In a preferred embodiment of the first and second aspects of the present invention, the particles are silica particles, preferably having a diallleter of between 20 to 100 nm. Silica is cheap and is readily available as a connircial powdered product, known as aerosil flamed silica. whose powder particles are of a suitable size. Although silica and silica-based
particles are preferred, other materials of hydrophobic character which can be prepared in a sufficiently small particulate size could be used. Examples include oxides such as titanium dioxide.
The optional modifying step can be any means to form active functional groups that will allow the particles to chemically bond or cross- link to each other and to the surface to be coated. The present inventors have found that when using silica particles, silylalkylmethacrylate groups such as silylpropylmethalcrylate (or related) functional groups, or a mixture of those functional groups and passive silylalkyl groups are particularly suitable. The methacrylate functional groups act as centres for chemically linking the particles. There are also silica particles colllmercially available that have suitable functional groups thereon such that step (a) can be optional.
Chemical cross-linking of the functional groups on the particles may be achieved by the addition of a copolymerisation nionomer. such as styrene, to link methacrylate functional groups from one particle to methacrylate functional groups of another.
Alternatively, cross-linking of the particles is also be possible without the use of Inonomers. if contact between methacrylate groups from different particles is favourable. It will be appreciated that this will depend on the length of the alkyl chain of the functional group.
Either type of cross-linking can be activated photolytically by means of ultra-violet radiation or by using a radical initiator such as benzoyl peroxide or diethoxyacetophenol.
Preferably, the particles (and the polymer, when used) are applied to the surface in a slurry. This can be achieved using a solvent, preferably an organic solvent. One solvent found to be particularly suitable for silica particles is hexane. It will be appreciated, however, that other solvents would also be suitable.
The present inventors have found that the cross-linking of the particles when applied to a surface results in the attachment of the particles on the surface thereby forming a hydrophobic film.
In order to obtain a more durable coasting, the use of a non-silicone polymer is preferred. A particularly suitable non-silicone polymer is polyurethane. Preferably, the polyurethane is formed by the reaction of di- or poly-isocyans with polyols. Isocyanates may react, under suitable
conditions, with the active hydrogen atoms of the urethane linkages to fonn biuret.
In a preferred method, methylene bis(phenyl isocyanate) (MDI) was chosen to react with polydimethylsiloxane (PDMS) with hydroxyl groups tenninated or 2,2,3,3,4,4,5 ,5-octafluoro-1,6-hexanediol. The produced prepolymer has some free isocyanate groups on the chain. Toluene or ethyl acetate can be used as suitable solvents. The prepolyiner is mixed with silica powder so that the isocyanate groups on the prepolymer can react with the silanol groups on the powder surface to chemically bond the particles together and to the surface to be coated.
The method of the present invention produces hydrophobic films with a contact angle of water of at least 1500, preferably at least 1600, and most preferably about 165".
In a third aspect, the present invention consists in an object having at least a portion of its surface coated with a hydrophobic film applied by the method according to the first or second aspects of the present invention.
In a fourth aspect, the present invention consists in the use of the methods according to the first or second aspects of the present invention to coat at least part of the surface of an object.
The surfaces to be treated can include metals, alloys, glasses, papers, ceramics, polymers, composites, and other materials. The surface treatment can be used to inhibit corrosion, formation of crystallisation centres in water pipe lines, closed heat exchangers, tubular boilers, chillers and refrigerators which utilise water, brine solutions, inorganic acids, alkalies, other electrolytes, and other corrosive fluids as coolants. The treatment can be used to prevent icing on surfaces, to produce anti-griping hydrophobic coatings for aboveground fixed facilities such as buildings and other structures, to provide anti-icing and anti-corrosion coatings for aircraft; or to provide anti-icing, anti-fouling and anti-corrosion coatings for maritinle and inland waterway vessels.
Other uses include to improve the resistance of metallic roofs to microflora colonisation; to provide water resistance. waterproofing, and ecological protection to slate and tile; to provide ecologically sound rubberoid and bitumen roofing felt; to provide water and moisture repellent cork material from paper, container board polyurethane foam and shavings.
The coating may be used for extending the survivability, perfonuance, and reliability of instruments and equipment.
Other uses include to protect granular construction materials including cement, alabaster and chalk for long-term storage, particularly in high hulllidity regions; extend the life cycle of lerro-concrete, concrete stone, brick, concrete cinder block and wooden structures and buildings exposed to weather conditions and microorganisms; protect frescoes, mouldings, buildings of architectural significance, gypsum structures, church and mosque domes, works of art and manuscripts from atnlospheric moisture and microorganisms.
Still other uses envisaged include to reduce drag for vessels such as canoes, yachts, ships, and other watercraft; improve the performance, reliability and corrosion resistance of cooling systems in internal combustio engines utilising closed heat exchangers having liquid heat transfer agents; provide anti-corrosive and anti-icing coatings for undercarriages of vehicles such as tractors and combines and for agricultural machinery in general. The coating may reduce labor intensity and improve product quality for laminated plastic products by reducing mechanical adhesion between the surfaces of compression moulds, punches, dies and product surfaces; assist the uniform distribution of dispersed fillers, such as wool, carbon fibres, fibreglass, artificial fibres, both in solution and suspension; encapsulate hydrophilic liquids including toxic liquids; moisture seal materials; provide "dry water" fire fighting materials; provide surfaces for facilitating pipeline transfer of granular material such as ore, coke, fertilisers or coal.
The film according to the present invention may also be used to waterproof building foundations and structures and radioactive waste storage facilities; extend the operating service life of water cooling towers; protect railroad ties from lllicroflora; provide anti-icing coatings for cooling chanlbers. refrigerators and chillers; extend the life cycle of hydroelectric power dams; improve the efficiency of wind driven motors; improve performance characteristics of concrete and asphalt in open roadways, highways and thoroughfares; increase the life cycle of automobile tires; adsorb ions of heavy metals and rndionuclides; provide anti-abrasive lubricants for ball bearings and other working parts; provide water repellent footwear; waterproof electric motors and electric insulators; waterproof pressurised suits such as diving suits.
Other uses include to conserve paper, books, securities and documents in archives and storage facilities; provide hydrophobic black paste used for waterproof ink in pens; provide hydrophobic denim; provide hydrophobic tents, clothing, umbrellas, raincoats, and suits; provide hydrophobic funnel filters for use with gasoline and petroleum products; provide hydrophobic sails; provide hydrophobic fishing nets; waterproof fur products; render wallpaper water resistant; conserve die colours; provide skin protection from burns, acids, bases, other electrolytes, rocket fuels, highly toxic materials and flammable solutions; provide hydrophobic foam for ecological protection of the atmosphere and fauna and flora against accidental spills of highly toxic poisons and rocket fuels; protect electric train current collectors from ice and corrosion; provide de-icing of airport runways; preserve vegetables and fruits under long-term storage; provide water, moisture and acid resistant footwear; provide waterproofing of printed circuit boards; provide waterproof lubricants to improve sky slip; localise vaporisation of corrosive fluids in emergencies; improve longevity and performance reliability of pumps and pipelines carrying inorganic acids, alkalies and other corrosive llledia; encapsulate acid, base, other electrolyte and other corrosive solutions as well as hydrocarbons for transport and storage; provide hydrophobic anti- aggloineration agents; preserve instruments. equipment and devices by nieans of conservation lubricants; and protect radio repeater and radar antennas from corrosion and icing Throughout this specification, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element or integer or group of elements or integers but not the exclusion of any other element or integer or group of elements or integers.
In order that the present invention Illay be more clearly understood, preferred forms will be described with reference to the following examples and the accompanying drawings.
Brief Description of Drawings Figure 1 shows a XPS spectrum of a powder-only coating; Figure 2 shows a XPS spectrum of a powder-polynwer mixture coating; Figure 3 shows a SIMS spectrum of a microbiological test sample of powder-polymer mixture coating before washing; and Figure 4 shows a SIMS spectrum of a microbiological test sample of powder-polymer mixture coating after washing.
Modes for Carrying Out the Invention In one preferred method, silica powder is treated with a trimefloxysilylalkylmethacrylate such as trimethoxysilylpropyllllethacrylate (or a related compound] and subsequently treated with trimethoxysilylalkane. The treatment with the trimethoxysilylpropylmethacrylate bonds silylpropylmethacrylate groups to the silica. The treatment with trimethoxysilylakane bonds passive silylalkane groups to the silica which increase the hydrophobicity of the silica particle.
Alternatively, both the trimethoxysilylpropylmethacrylate and the trimethoxysilylalkane can be used simultaneously to attach the necessary groups to the silica.
The modified silica particles are then placed in a suitable solvent. The particles may be suitably dispersed in a slurry in hexane, for example. The slurry can be stirred and sonicated at 40 Hz to improve the dispersion of the particles in the slurry. A suitable surface is then coated with the slurry and the slurry is treated so that the particles cross-link to bind themselves together and to the surface itself.
The cross-linking may be achieved by the addition of a co- polymerisation monomer such as styrene to link the functional methacrylate groups from one particle to functional methacrylate groups of another.
In an alternative embodilllent, cross-linking of the particles may be possible without the use of monomers if contact between methacrylate groups from different particles is favourable. This will depend on the length of the alkyl chain in the silylalkylmethalcrylate group.
Cross-linking can be activated either photolytically using ultra-violet radiation or by using a radical initiator such as benzoylperoxide or diethoxyacetophenol.
The balance between the ratio of functional groups to passive groups on the silica particles should be such to optimise the linking of the particles and thus the mechanical strength of the coating whilst maintaining sufficient passive groups to optimise the hydrophobicity of the coasting.
The alkyl chain linking the silyl groups and the methacrylate functional group also has a bearing on the characteristics of the coasting, and whether cross-linking is possible without the use of monomers.
Wsorbers may be used to facilitate the curing of the films under ultra- violet light if cross-linking is activated photolytically.
The preferred length for the chemical bond connecting the individual particles is about 3A.
PREPARATION OF HYDROPHOBIC FILMS Several steps to improve the hydrophobicity and durability of the film were carried out. These steps included using fun1ed silica powder to produce rough surface in order to increase hydrophobicity, and employing non- silicone polymer (adhesive) to improve the durability of the film.
Method I - powder-only deposition This method involves a slurry of a known concentration of silica powder in hexane at concentration of 2.0 - 2.7% (wt) powder, which was left in an ultrasonic bath to ensure dispersion and aggregate breakdown, and the slurry was then deposited onto a spinning substrate at a spinning rate of from 500 - 2000 rpm. Different concentrations of the slurry and different spinning speeds were investigated to obtain an optimal hydrophobic film with the highest correct angle.
By using this technique, it was possible to obtain a film with contact angle of water approximately 1650. The durability of the film, however, was not ideal in all situations.
Method II - powder and polymer mixture deposition To improve the durability of the hydrophobic film, polyurethane was introduced to act as the adhesive which further links the silica powder together by chemical bonding.
Polyurethane are polymers formed by the reaction of di- or poly- isocyans with polyols:
polyol + diisocyante < polyurethane Isocyanates may react, under suitable conditions. with the active hydrogen atoms of the urethane linkages to form biuret. polyurethane + isocyanate ~ biuret The method involved preparing prepolymer by reacting polyol with stoichiometrical excess of diisocyanates so as to leave some free isocyanate groups on the prepolymer's chain. The synthesised prepolyurethane then reacts with silanol groups on hydrophilic powder surface to make powder and polymer chemically linked together.
The following examples describe more specific methods of bonding silica powder particles together by polyurethane. In a preferred method, 125 grams of methylene bis(phenyl isocyanate) (MDI) was chosen to react with 75 grams of polydimethylsiloxane (PDMS) with hydroxyl groups terminated (viscosity of 90-150 cst) or 121 grams of 2,2,3,3,4,4,5,5-octafluoro-1,6- hexanediol in the presence of 1-10% (wt) of diethanolamine as the catalyst.
The produced prepolymer has some free isocyanate groups on the chain.
Toluene or ethyl acetate was chosen as the solvent, making a concentration as 20-50% (wt) of polymer. The prepolynier was mixed with hydrophilic silica powder (1:1 - 1:2% wt/wt) so that the isocyanate groups on the prepolymer can react with the silanol groups on the powder surface to chemically bond the particles together and to the surface.
The substrates used for method I and method II were rubber, aluminium plates and glass plates.
By using this method, it is possible to obtain a hydrophobic film with the contact angle of water of 1600 and having good durability.
Microbiological Tests The test was carried on in a container full of fresh sea water. The substrates with the hydrophobic coatings were immersed in the sea water which was bubbled with air and added with nutrient broth every half month to provide the food for microorganisms present. The test was carried out over three months. At the end of the test, the substrates were taken out of the sea water and washed by flowing water. The growth and accumulation of the marine microorganisms on the substrates were assessed by the coverage and the adhesion of the marine microorganisms.
EXPERIMENTAL RESULTS Contact Angle Measurements Contact angle measurement was carried out by using the sessile drop technique due to the ease and accuracy of the method.
The largest contact angle tested for the coatings prepared by method I was 165° and for the coatings prepared by method II was 1600.
Durability It was found that the durability of the powder and polymer coatings was much better than the powder-only film by which powder is physically bonded together. The findings were reinforced by the microbiological test data after 3 months by putting the films under seawater. The powder-only coatings were partly destroyed due to the weaker physical bonding between the powder and the substrate. During the 3-month test, some of the powder coating was removed from the substrate and floated on the surface of seawater. The polyurethane-powder coatings, however, remained intact, even after microorganisms growing on the film surface were washed off by flowing water.
Resistance to Microorganism Attachment Due to the improvement of the film durability, the resistant of the coatings to the microbiological growth was also improved. Unlike the powder-only coatings for which some area of the substrate was exposed to the environment during the test, the powder-polymer coatings were firmly bound to the substrate so that all of the substrate was covered by the
resistant substance after prolonged exposure to sea water. After three months, the attached microorganisms were very easily removed from the powder-polymer coatings by flowing water.
Instrumental Analysis of Surface Coatings Surface analysis technique were used to determine the chemical composition and surface images of the hydrophobic coatings. Figures 1 and 2 are XPS spectra of powder-only coatings and powder-polymer mixture coatings. respectively. Figures 3 aiid 4 are spectra of SINUS oil the microbiological test samples before and after washing by flowing water.
Many hydrocarbon peaks in the spectrum before washing belong to the microorganisms. and after washing the peaks disappear.
It ill be appreciated by persons skilled iii the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadlv described. The present embodiments are. therefore, to be considered in all respects as illustrative aiid not restrictive.