CA2057250C - Adsorbed monomolecular film and method of manufacturing the same - Google Patents
Adsorbed monomolecular film and method of manufacturing the sameInfo
- Publication number
- CA2057250C CA2057250C CA002057250A CA2057250A CA2057250C CA 2057250 C CA2057250 C CA 2057250C CA 002057250 A CA002057250 A CA 002057250A CA 2057250 A CA2057250 A CA 2057250A CA 2057250 C CA2057250 C CA 2057250C
- Authority
- CA
- Canada
- Prior art keywords
- group
- integer ranging
- monomolecular film
- substrate
- active material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/18—Processes for applying liquids or other fluent materials performed by dipping
- B05D1/185—Processes for applying liquids or other fluent materials performed by dipping applying monomolecular layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/261—In terms of molecular thickness or light wave length
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
Abstract
The invention seeks to provide a method of forming a monomolecular film of fluorine-containing molecules on a substrate surface such that the film has an uniform thickness with minimal surface irregularities and is substantially pin hole free. The invention also provides for a substrate obtained by using the same method which has excellent water- and oil-repelling, anti-fogging, and anti-contaminating properties. The monomolecular film is formed on the substrate surface either directly or via a given protective film. The monomolecular film coating is characterized by a plurality of different chlorosilane-based surface active materials which are different in molecular length have a fluorine group. The surface irregularities of the film are generally confined to the molecular level.
Description
ADSORBED MONOMOLECULAR FILM AND
METHOD OF MANUFACTURING THE SAME
FIELD OF THE INVENTION
This invention relates to functional monomolecular films and, more particularly, to water-repellent, oil-repellent, anti-fogging and/or anti-contaminating films. More particularly, this invention relates to materials such as metals, ceramics, plastics, glass, etc. with a fluorine film coating.
BACKGROUND OF THE INVENTION
Heretofore, for improving the water- and oil-repelling properties of substrate surfaces, it has been a known practice to coat silicon-based surface active agents onto substrate surfaces or fluorocarbon-based polymer suspensions onto substrate surfaces.
Generally, a material with a fluorine resin coating is obtained by making the surface coarse by means of electrolytic etching or surface roughening to increase adhesion with a fluorine-based polymer. The surface is coated with a fluorine-based polymer suspension, followed by baking.
The prior art substrate has improved water- and oil-repelling properties and can be readily manufactured. However if the film coating on the substrate surface is insufficiently thin, it results in generation of pin holes, so that ~ ~ 5 7 ~ 5 0 sufficient water- and oil-repelling properties cannot be obtained. In addition, even if the film coating is sufficiently thick, its water- and oil-repelling properties are sometimes inadequate.
Furthermore, where a water-repelling, oil-repelling film is provided on a transparent substrate such as a glass substrate, the transparency thereof is deteriorated due to film thickness that is needed.
In addition, the surface and fluorine-based polymer coating are weakly coupled together, for there are no chemical bonds between the two. Therefore, when the material is used for a substantially long time, the adhesion deteriorates resulting in a separation of the fluorine-based coating from the surface of the material.
Therefore, a material with a fluorine-based coating which is substantially free of pin holes, is uniform in thickness, and the excellent water- and oil-repelling properties is highly desirable.
SUMMARY OF THE lNv~N-llON
In one aspect, the invention provides a monomolecular film of at least two different molecules having at one end fluorinated alkyl groups with different molecular lengths and being at the outer end covalently bonded through an -Si- bond to a surface of a substrate either directly or via an inner layer, wherein:
the monomolecular film has surface irregularities which are confined to a molecular level, and the surface of the substrate, before the monomolecular A ~
METHOD OF MANUFACTURING THE SAME
FIELD OF THE INVENTION
This invention relates to functional monomolecular films and, more particularly, to water-repellent, oil-repellent, anti-fogging and/or anti-contaminating films. More particularly, this invention relates to materials such as metals, ceramics, plastics, glass, etc. with a fluorine film coating.
BACKGROUND OF THE INVENTION
Heretofore, for improving the water- and oil-repelling properties of substrate surfaces, it has been a known practice to coat silicon-based surface active agents onto substrate surfaces or fluorocarbon-based polymer suspensions onto substrate surfaces.
Generally, a material with a fluorine resin coating is obtained by making the surface coarse by means of electrolytic etching or surface roughening to increase adhesion with a fluorine-based polymer. The surface is coated with a fluorine-based polymer suspension, followed by baking.
The prior art substrate has improved water- and oil-repelling properties and can be readily manufactured. However if the film coating on the substrate surface is insufficiently thin, it results in generation of pin holes, so that ~ ~ 5 7 ~ 5 0 sufficient water- and oil-repelling properties cannot be obtained. In addition, even if the film coating is sufficiently thick, its water- and oil-repelling properties are sometimes inadequate.
Furthermore, where a water-repelling, oil-repelling film is provided on a transparent substrate such as a glass substrate, the transparency thereof is deteriorated due to film thickness that is needed.
In addition, the surface and fluorine-based polymer coating are weakly coupled together, for there are no chemical bonds between the two. Therefore, when the material is used for a substantially long time, the adhesion deteriorates resulting in a separation of the fluorine-based coating from the surface of the material.
Therefore, a material with a fluorine-based coating which is substantially free of pin holes, is uniform in thickness, and the excellent water- and oil-repelling properties is highly desirable.
SUMMARY OF THE lNv~N-llON
In one aspect, the invention provides a monomolecular film of at least two different molecules having at one end fluorinated alkyl groups with different molecular lengths and being at the outer end covalently bonded through an -Si- bond to a surface of a substrate either directly or via an inner layer, wherein:
the monomolecular film has surface irregularities which are confined to a molecular level, and the surface of the substrate, before the monomolecular A ~
2~ 572SO
film is formed, is hydrophilic or has been made hydrophilic.
Another aspect of this invention is to provide a process of manufacturing an adsorbed monomolecular film by a chemical adsorption process comprising the steps of:
preparing a coating composition which comprises a blend surface active material in a non-aqueous solvent, the blend surface active material comprising two molecules differing in molecular chain length and each having at one end a halosilane or alkoxysilane group and at the other end a fluorinated alkyl ~0 group; and contacting the coating composition with a substrate having at a surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane, and causing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming a monomolecular film on the substrate surface.
One embodiment of the process, comprises the steps of:
preparing a coating composition constituted by a surface active material in a non-aqueous solvent, the surface active material having at one end a halosilane or alkoxysilane group, and contacting the coating composition with a substrate having at the surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane, and causing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming an inner layer on the substrate surface;
adding a hydroxyl group (-OH), an amino group (-NH2), or an imino group (-NH) on the inner layer surface; and Z ~ ~ 7 ~ 5 0 preparing a coating composition which comprises a blend surface active material in a non-aqueous solvent, the blend surface active material comprising two molecules differing in molecular chain length and each having at one end a halosilane or alkoxysilane group and at the other end a fluorinated alkyl group, and contacting the coating composition with the inner layer having at the surface thereof the hydroxyl, amino or imino group (i.e. an active hydrogen capable of reacting with the halosilane or alkoxysilane), thereby laminating a monomolecular film on the inner layer surface.
The adsorbed monomolecular film is chemically bonded by a covalent bond each containing a -Si- group to the surface of a substrate either directly or via an inner layer and the adsorbed monomolecular film is constituted by at least two different molecules having different molecular lengths.
It is preferable in this invention that the adsorbed monomolecular film is formed as a lamination on the inner layer and the inner layer has a substantially uniform ~ ~7 250 thickness.
It is preferable in this invention that the inner layer is directly bonded by covalent bonds each having a -Si- group to the substrate surface and is also bonded by covalent bonds each having a -Si- group at the outer adsorbed monomolecular film.
It is preferable in this invention that the adsorbed monomolecular film has molecular surface irregularities to a molecular level extent.
It is preferable in this invention that the adsorbed monomolecular film is either water-repelling, oil-repelling, anti-fogging property or an anti-contaminating.
It is preferable in this invention that the adsorbed monomolecular film is comprises at least one monomolecular compound selected from the group consisting of the formula [I]
[I] F (C F2 ) m (C H2 ) n S i ( R q ) (~3-q ) where m represents an integer ranging from 1 to 15, n represents an integer ranging from O to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from O
to 2, and R represents an alkyl group or an alkoxyl group.
[II] F (C F 2 ) s (C H2 ) t A ( C H 2 ) p S i (R q ) ( 03-q ) where s represents an integer ranging from 1 to 8, t represents an integer ranging from O to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from O to 2, A represents a member of a group consisting of an oxy group(-O-), a carbonyl group (~C=O), a carboxyl-ester group (-COO-) and dimethylsilylene group (- S i (C H 3 ) 2 -) and R represents an alkyl group or an alkoxyl group.
It is preferable in this invention that the molecules of the blend surface active material have an alkyl fluoride group.
It is preferable in this invention that the molecules of the blend surface active material has at one end a trifluoromethyl group (-CF3 ) and the other end a chlorosilane group (-SiCl).
It is preferable in this invention that the blend surface active material contains a silane surface active material represented by the formula;
F (C F2 ) m (C H 2 ) n S i (R q ) (X3-q ) where m represents an integer ranging from 1 to 15, n represents an integer ranging from O to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from O
to 2, and R represents an alkyl group or an alkoxyl group, X
represents a halogen atom or an alkoxyl group, and by the formula;
F (C F2 ) s (C H2 ) t A (C H2 ) p S i (Rq ) (X3_q ) where s represents an integer ranging from 1 to 8, t 20~250 represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from O to 2, X represents a halogen atom or an alkoxyl group, R represents an alkyl group or an alkoxyl group, A represents a member of a group consisting of an oxy group (-O-), a carbonyl group ( ~C=O), a carboxyl-ester group (-COO-) and dimethylsilylene group ( - S i ( C H3 ) 2 -) -BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a schematic sectional view, enlarged inscale to the molecular level showing an inner layer having vinyl groups on the surface of a substrate as described in Example 1 of this invention.
Figure 2 is a schematic sectional view, enlarged in scale to the molecular level showing the inner layer forming hydroxy groups on the surface of a substrate as described in Example 1 of this invention.
Figure 3 is a schematic sectional view, enlarged in scale to the molecular level showing the inner layer forming amino groups on the surface of a substrate as described in Example 1 of this invention.
Figure 4 is a schematic sectional view, enlarged in scale to the molecular level showing the laminating monomolecular film on the inner layer surface of a substrate as described in Example 1 of this invention.
~ ~ 5 ~ ~ S ~
Figure 5 is a schematic sectional view, enlarged in scale to the molecular level showing the monomolecular film on a substrate as described in Example 1 of this invention.
Figure 6 is a schematic sectional view, enlarged in scale to the molecular level showing the monomolecular film on the surface of nylon-6,6 substrate as described in Example 2 of this invention.
DETAILED DESCRIPTION OF THE lNV~L. ~lON
According to the invention, the above problems are solved by a water-repelling, oil-repelling, anti-fogging, and anti-contaminating film comprising a monomolecular film formed on a substrate surface and containing a fluorinated alkyl group, the monomolecular film having minimal surface irregularities wherein the irregularities are generally confined to the molecular level.
By incorporating onto the substrate surface a monomolecular film which contains a plurality of different fluorinated alkyl groups having different molecular lengths, a coating in the form of a monomolecular film can be obtained which has minimal surface irregularities. Typically, such surface irregularities are confined to the molecular level.
Because the surface has minimal irregularities and the molecules constituting the monomolecular film contain fluorine, the area of contact between water drops and the film surface can be reduced. Thus the film itself can have a very high water-repelling property. The film similarly repels oil drops, and therfore provides an improved oil-repelling property. With both these effects, the anti-fogging and anti-contaminating properties can also be improved.
The substrate to be used according to the invention is of such materials as pure metals, e.g., aluminum, copper and iron, alloys or like composite materials, semiconductors, fiber, cloth, fabric, fur, leather, wood e.g., silicon and germanium, glass and plastics. According to the invention, a hydrophilic substrate is used. Where the substrate is made of a common base metal or a semiconductor, it is made hydrophilic by a natural oxide film formed on its surface. In case of a relatively non-hydrophilic substrate such as a plastic substrate, a hydrophilic property is imparted by, for instance, a corona treatment, plasma treatment or an ion beam irradiation. Furthermore, with a relatively non-hydrophilic substrate, it is recommended to form a monomolecular film in advance of a surface active material having unsaturated carbon-carbon bond groups by using such means as a Langmuir-Blodgett's technique (hereinafter referred to as LB process) or a chemical adsorption process and then forcibly rendering the film hydrophilic by such means as causing breakage of the unsaturated bonds in an atmosphere containing oxygen, _ g _ .~.. . . .. . . .. . .
nitrogen, etc. This is preferred because many hydrophilic group~ are formed on the surface of the substrate, and a high concentration of monomolecular film can be obtained at the surface of the substrate. As a reagent for rendering the substrate surface hydrophilic the following compounds may be used C H2 = C H - ( C H 2 ) n - S i C 13 and C H 2 = C H - ( C H 2 ) n - C O O H (where n represents an integer desirably about 10 to 20). The monomolecular film may be formed by ordinary means such as the LB process or the chemical adsorption process. Unsaturated bonds may be broken by ordinary means such as treatment with an electron beam, X-rays, gamma-rays, ultraviolet rays or an ion beam, plasma or corona treatment.
However, plastics having _NH groups such as polyamide or polyurethane substrates are not necessary in a surface oxygen treatment. Because as _NH groups have active hydrogen, it is relatively easy to reduce the groups by initiating the dehydrochloric acid reaction using the chlorosilyl groups of surface active material.
The film coating according to the invention is formed by utilizing a very thin monomolecular film, and therefore the initial surface state of the substrate may be maintained as such.
The monomolecular film according to the invention may 20~7250 be formed on the substrate either directly or via a protective film or the like. Particularly, the monomolecular film according to the invention is suitably formed via such a functional film as a protective film, an anti-reflection film or an infrared-absorbing film. By doing so, it is possible to maintain high anti-reflecting or infrared-adsorbing properties for long time and also obtain a protective or like functional effect in addition to the nater-repelling, oil-repelling, anti-fogging and anti-contaminating effects owing to the monomolecular film.
According to the invention, on a substrate surface is formed either directly or via a given film such as a protective film a water-repelling, oil-repelling, anti-fogging anti-contaminating film in the form of a monomolecular film, which contains a plurality of different kinds of fluorine (F) containing group having different molecular lengths, the surface of which is predominantly confined to molecular irregularities. The monomolecular film may be formed by the LB process, the chemical adsorption process or any other usual process. In the chemical adsorption process, the reagent is adsorbed via chemical bonds to the substrate, and therefore this process is preferred for maintain highly close contact with the substrate. Moreover high mechanical strength of the monomolecular film can be obtained.
~i 7 ~ ~ ~
Where the LB process is used to form the monomolecular film according to the invention, a carboxylic acid (-COOH), a carboxylic acid salt, an ester, a trialkoxysilane, a trihydrosilane, etc. having a fluorinated alkyl group in a molecule may be used.
Where the chemical adsorption process is used to form the monomolecular film according to the invention, preferably used are fluorochlorosilane-based surface active materials containing a fluorinated alkyl group and a chlorosilyl group, fluorotitanium-based surface active materials containing a fluorinated alkyl group and a titanate group, fluorothiol surface active materials having a fluorinated alkyl group and a thiol group.
As for the fluororchlorosilane-based surface active materials to be used according to the invention, they are suitably those represented such as in the formulas [A] and [B]. These fluorochlorosilane-based surface active materials are suitable because they are readily available and have pronounced water-repelling, oil-repelling, anti-fogging and anti-contaminating effects.
They are suitably those represented by the formulas;
CF3(cH2)2si(cH3)2(cH2)l5sicl3l CF3(cF2)3(cH2)2si(cH3)2(cH2)9sic13, C F 3 C H 2 ~ (C H 2 ) 15s i C l3 C F 3 C O O (C H 2 ) 15s i C 13 , C F 3 (C F 2 ) 9 (C H 2 ) 2 S i C l 3 , C F 3 (C F 2 ) 7 (C H 2 ) 2 S i C l 3 , and C F 3 (C F 2 ) 5 (C H 2 ) 2 S i C l 3 -As the fluorotitanium-based or fluorothiol-based surface active materials for producing the monomolecular film according to the invention by the chemical adsorption process, those compounds obtained by substituting titanate or thiol for the chlorosilyl group of the above chlorosilane-based surface active material may be used.
Where an alkoxysilane-based surface acive material is used, adsorption is effected with an alcohol removal reaction when forming a chemically adsorbed monomolecular film. When a fluorothiol-based surface active material is used, adsorption is effected with a hydrous reaction. These surface active materials are therefore preferred to surface active materials having chlorosilyl groups, because they do not cause damage to even metal substrates.
The invention can widely be applied to the following uses. Materials made of metal, ceramic or plastic, glass, wood, stone, fiber, cloth, fabric, fur, leather etc. are applicable to the substrate. The surface of the substrate can also be coated with paint or the like.
2057~50 Examples of cutlery: a kitchen knife, scissors, a knife, a cutter, a graver, a razor, hair clippers, a saw, a plane, a chisel, a gimlet, a badkin, bite (cutting tools), a edge of a drill, a edge of a mixer, a juicer, a blade of a mill, a blade of a lawn mower, a punch, a straw cutter, a staple of a stapler, a can opener or a surgical knife and the like.
Examples of needles: an acupuncture, a needle, a sewing needle, a matting needle, an injection needle, a surgical needle, a safety pin and the like.
Examples of products in pottery (ceramics) industry:
products made of pottery, glass, ceramics or an enameled products. For example, sanitary potteries ( a chamber pot, a wash-bowl, a bathtub, etc.), tableware ( a rice-bowl teacup, a dish (plate), a bowl, a teacup, a glass, a bottle, a coffee-pot (siphon), a pan, an earthenware mortar, (a cup and the like), vases ( a flower bowl, a flowerpot, a bud vase and the like), water tanks (a breeding cistern, an aquarium water tank and the like), chemical experiment appliances ( a beaker, a reactor vessel, a test tube, a flask, a laboratory dish, condenser, a mixing rod, a stirrer, a mortar, a bat, a syringe, etc.) a roof tile, enameled ware, an enameled washbowl, an enameled pan and the like.
Examples of molding parts: dies for press molding, dies for cast molding, dies for injection molding, dies for , i, , ,. ,.. " , . . .. . . . .
transfer molding, dies for compression molding, dies for transfer molding, dies for inflation molding, dies for vacuum molding, dies for blow forming, dies for extrusion molding, dies for fiber spinning, a calendar processing roll and the like.
Examples of forming molds for food: cake, cookies, bread-baking, chocolate, jelly, ice cream, an oven ware, an ice tray and the like.
Examples of cookware: kitchen utensils (a pan and a pot), a kettle, a pot, a frying-pan, a hot plate, a gridiron net, a takoyaki plate and the like.
Examples of resin(s): a polyolefin such as a polypropylene and polyethylene, a polyvinylchloride plastic, a polyamide, a polyimide, a polyamideimide, a polyester, an aromatic polyester, a polycarbonate, a polystyrene, a polysulfide, a polysulfone, a polyethersulfone, a polyphenylenesulfide, a phenolic resin, a furan resin, a urea resin, a epoxy resin, a polyurethane, a silicon resin, an ABS
resin, a methacrylic resin, an acrylate resin, a polyacetal, a polyphenylene oxide, a polymethylpentene, a melamine resin, an alkyd resin, an unsaturated polyester cured resin and the like.
Examples of rubber(s): a styrene-butadiene rubber, a butyl rubber, a nitril rubber, a chloroprene rubber, a , ~ .. .. ..
2057~0 polyurethane rubber, a silicon rubber and the like.
Examples of household electric appliances: a refrigerator, a freezer, an air conditioner, a juicer, a mixer, a blade of an electric fan, a lighting apparatus, a dial plate, a dryer for a perm and the like.
Examples of sporting goods: skis, a fishing rod, a pole for the pole vault, a boat, a yacht, a surfboard, a fishing line, a float and the like.
Examples applying to vehicle parts:
(1) ABS resin: a lamp cover, an installment pannel, trimming parts, a protector for a motorcycle.
(2) Cellulose plastic: a car mark, a steering wheel (3) FRP (fiber reinforced plastics): a bumper, an engine cover (jacket) (4) Phenolic resin: a brake (5) Polyacetal: wiper gear, a gas valve (6) Polyamide: a radiator fan (7) Polyarylate (polycondensation polymerization by bisphenol A and pseudo phthalic acid): a direction indicator lamp (or lense), a cowl board lense, a relay case (8) Polybutylene terephthalate (PBT): a rear end, a front fender (9) Poly amino-bismaleimide : engine parts, a gear box, a wheel, a suspension drive system 20~72~0 (10) Methacrylate resin: a lamp cover lens, a meter pannel and its cover, a center mark (11) Polypropylene: a bumper (12) Polyphenylen oxide : a radiator grille, a wheel cap (13) polyurethane: a bumper, a fender, an installment pannel, a fan (14) Unsaturated polyester resin: a body, a fuel tank, a heater housing, a meter pannel.
Examples of office supplies: a desk, a chair, a bookshelf, a rack, a telephone stand table, a rule (measure), a drawing instrument and the like.
Examples of building materials: materials for a roof, and outer wall and interiors. Roof materials such as brick, slate and tin (a galvanized iron sheet) and the like. Outer wall materials such as wood (including processed manufactured wood), mortar, concrete, ceramic sizing, metalic sizing, brick, stone, plastic and metal like an aluminium. Interior materials such as wood (including processed wood), metal like an aluminium, plastic, a paper, fiber and the like.
Examples of building stones: granite, marble and others for use as a building,a building material, an architecture, an ornament, a bath, a grave stone, a monument, a gatepost, a stone wall, a paving stone and the like.
Examples of the others: a high resisting voltage insulator such as a thermos bottle, a power supplying insulator for a vacuum system machinery or a spark plug, which has high water-repellent, oil-repellent, anti-fogging and anti-contamination effects.
Specific examples of the process of chemical adsorption of a water-repelling oil-repelling anti-fogging, anti-contaminating film coating according to the invention will now be described with reference to Figures 1 to 5.
Example 1 As solution containing 80 % wt n-hexadecane, 12 % wt carbon tetrachloride and 8 % wt chloroform was prepared by using C H2 = C H - (C H2 ) 16- S i C l3 as a silane surface active material and dissolving the same to a concentration of 3 x 10 3 to 5 x 10 2 mol, and a tempered glass substrate 1, as shown in Figure 1, was dipped into this solution and held at room temperature for one hour. Since the surface of the substrate 1 contained hydroxyl groups, a reaction between the chlorosilyl groups of the chlorosilane-based surface active material and the hydroxyl groups, thus forming on the surface bonds represented such as the formula [1] .
, ~ ~ ~ 7 ~ ~ ~
CH2= CH -(CH2)l6-SiCl3 + (-OH) CH2= CH -(CH2)l6-lSi-O - + HC1 The tempered glass 1 was then washed by Freon 113*
to remove the material remaining on the surface without reaction, followed by washing with water or exposing to air to react with moisture in the air. The -SiCl group was changed to a -SiOH group as in formula [2].
CH2=CH--(CH2)l6--ISi--O-- + 2H20 OH
CH2=CH -(CH2)16-~i-O - + 2HC1 OH
Fonnu~[2 ]
Each silanol group (-SiOH) was then dehydrated and crosslinked to form a siloxan bond (-SiO-) as in formula [3].
* Trade-mark ~ 73466-15 O H
I
n CH2 = CH-- (CH2 ) 16--S i --O--I
O H
I
~n C H2 = C H-- (C H2 ) 16--S i --O-- + n H2 ~
I
o - Formula [3]
By the consecutive reaction, a single adsorbed monomolecular film 3 having vinyl (CH2 =CH-) groups 2 was formed to a thickness of about 2.5 nm such that it was chemically bonded (i. e., covalently bonded) to a protective film via oxygen atoms.
This glass substrate 1 was irradiated with about 3 Mrad. of X-rays in an atmosphere containing oxygen and also in an atmosphere containing nitrogen. Where the substrate 1 was irradiated in the oxygen-containing atmosphere, a monomolecular film 3' (inner layer), as shown in Figure 2, was obtained, which contained hydroxyl (-OH) groups 4 added to the vinyl groups 2. Where the irradiation was done in the nitrogen-containing atmosphere, a monomolecular film 3" (inner layer) was obtained, as shown in Figure 3, which contained , . . ~.
amino groups (-NH2 ) 5 added to the vinyl groups 2. The addition of the functional groups, i.e., the -OH, -NH2 and -NH groups, to the vinyl groups, was confirmed as a result of a FTIR analysis.
Subsequent to the addition of -OH groups, a solution containing 80 % wt n-hexadecane, 12 % wt carbon tetrachloride and 8 % wt chloroform was prepared by using C F3 (C F 2 ) 7 (C H 2 ) 2 S i C 13 and C F 3 C H 2 ~ (C H2 ) 15S i C l 3 as respective chemical adsorption materials and dissolving these reagents to respective concentrations of about 2 x 10 3 to 5 x 10 2 Mol and at a mixing ratio of 3 : 1 to 1 : 3, and the glass substrate 1 forming the monomolecular film 3', as shown in Figure 2, was dipped into the solution and held for one hour. Since -OH groups 4 were exposed at the surface of the substrate 1, the chlorosilic groups of the chlorosilane-based surface active material having fluorine and -OH groups 4 were reacted. Thus, bonds represented by formulas [4] and [5]
were produced on the surface substantially at the above mixing ratio. This reaction proceeded substantially the same as above in formulas [1] to [3].
... ~ .. . ~ ...... .... ~
2~57250 C F3 (C F 2 ) 7 (C H 2 ) 2 S i ~ - Formula [4]
O-O-I
C F3 C H2 0 (C H2 ) 15 S i O - Formula [5]
I
Thus, a high concentration monomolecular lamination film 7 can be obtained on the surface of the glass substrate 1, as shonn in Figure 4. The film 7 includes an adsorbed monomolecular film 6 which has a fluorine group and surface irregularities which are generally molecular irregularities.
The adsorbed monomolecular film is chemically bonded (i. e., covalently bonded) to the inner layer 3 ' .
The water wetting angle measured at the surface of the adsorbed monomolecular film 6 was from 140 to 150 degrees.
The measured value showed an improvement by about 20 to 30 degrees from 120 degrees, which was obtained by using only a single kind of fluorosilane-based surface active material.
The resultant glass therefore can be used to obtain a wiper-free vehicle window glass and to prevent fogging on, for ~ ~7 ~
instance, glass lens surfaces.
These effects can be obtained by forming a monomolecular film containing fluorinated alkyl groups on the outermost substrate surface wherein the fluorinated alkyl groups have different molecular lengths such as formulas 4 and 5, with the surface being substantially pin hole free.
Where no intermediate monomolecular film is necessary between the surface water-repelling, oil-repelling film and the glass substrate, a singularly adsorbed monomolecular film 8 containing fluorine may be formed on a glass surface directly, as shown in Figure 5, by using a chlorosilane-based surface active material having fluorine and a mixing ratio of, for example, 1:1. Such a glass was shown to have sufficient water- and oil-repelling properties.
Where a plurality of intermediate monomolecular films are necessary, the steps of chemical adsorption and subsequent radiation irradiation are repeated a number of times corresponding to the necessary laminated film number.
For example CH2= CH(CH2)16-SiCl3 and a plurality of different chlorosilane-based surface active materials having fluorinated alkyl groups with different molecular lengths can be adsorbed as adsorption reagents. By doing so, a water-repelling, oil-repelling film having a single fluorine-containing adsorbed monomolecular film can be formed on a ~A ~
f~ 73466-15 glass surface via a number of intermediate laminated monomolecular films.
In the above example, as to the reagent for forming the outermost surface adsorbed monomolecular film containing fluorine and dimethylsilylene or oxygen atom or a carboxy ester the following can be used;
CF3(cH2)2si(cH3)2(cH2)l5sicl3/
F(CF2)4(CH2)2Si(CH3)2(CH2)gSiCl3 CF3COO(CH2)1sSicl3 CF3(CF2)g(CH2)2sicl3 CF3(CF2)5(CH2)2sicl3 Example 2 A chemically adsorbing solution was prepared by using Freon 113 , CF3(CF2)7(CF2)2SiCl3 and CF3CH2 O(CH2)15SiCl3 as silane surface active materials. The surface active materials were each dissolved to a concentration of 1 wt. A nylon-6,6 substrate was dipped into this solution and held at room temperature for one hour. Since the surface of the nylon-6,6 substrate contained imino groups (=NH), a reaction between the chlorosilyl groups of the chlorosilane-based surface active material and the imino groups formed surface bonds as represented in the formulas [6] and [7].
This reaction proceeded substantially as in formulas [1] to [3].
* Trade-mark r~
CF3(cF2)7(cH2)2ri- N-- Fo~n~a[6]
CF3CH2O(CH2)1s~i- I--Fonn~a[7]
Thus, a high concentration monomolecular film 9 can be obtained on the surface of the nylon-6,6 substrate 10, as shown in Figure 6. The adsorbed monomolecular film 9 has a fluorine group and surface irregularities which are generally molecular surface irregularities. The adsorbed monomolecular film is chemically bonded (i.e., covalently bonded) to the substrate 10.
The water wetting angle measured at the surface of the monomolecular adsorbed film 9 was from 140 to 150 degrees.
A water-repelling, oil-repelling film having a single fluorine-containing monomolecular adsorbed film was formed on the substrate 10.
Example 3 This example, like Example 1, concerns the formation ~ ~ ~ 7 ~
of the water-repelling, oil-repelling, anti-fogging, anti-contaminating film coating by the LB process using a tempered glass substrate.
A blend surface active material was obtained by mixing two different surface active materials, i.e., CF3(CF2)7(CH2)2COOH and CF3CH2O(CH2)15COOH at a mixing ratio of 1:1, and 10 mg was dissolved in 100 g of chloroform. The solution was then quietly developed on the water surface.
A tempered glass substrate as in Example 1 was then dipped at a speed of 1 cm/min. under a pressure of 50 mN/m and then raised.
As a result, a film coating having molecular surface irregularities and containing fluorinated alkyl groups was formed on the tempered glass substrate. This film coating had the same water-repelling property as the film obtained in Example 1.
The water-repelling effect obtained in this example is attributable to the fact that like Example 1 the monomolecular film containing fluorinated alkyl groups is formed as the outermost surface layer on the substrate. The fluorinated alkyl groups are characterized by having different constituent molecules, different molecular lengths.
Any of the above examples can also use two different surface active materials in combination. By using three or more different reagents, a monomolecular film having three or more different reagents can be obtained. Such a monomolecular film has similar water- and oil-repelling effects.
Where a glass surface has a protective film or anti-reflection film such as metal or a metal oxide film, or an infrared-adsorbing film such as color formed infrared film, a chemically adsorbed film can be formed by appropriately controlling the adsorption time so long as the surface has hydrophilic groups such as hydroxy groups.
Adsorbed films can be obtained under similar conditions by using, in lieu of the above chlorosilane-based surface active materials, fluorotitanate-based surface active materials such as a combination Of F ( C F 2 ) 8 S i (C H3 ) 2 (C H2 ) 9 T i 0 C H (C H3 ) 2 and C F3 (C F2 ) 9 (C H2 ) 2 T i 0 C H (C H3 ) 2, or F (C F2 ) 4 (C H2 ) 2 S i (CH3 ) 2 (CH2 ) 9 T i C 13, CF3 (CF2 ) 5 ( C H2 ) 2 S i T i 3, or a fluorothiol-based surface active material such as a combination of F (C F 2 ) 4 (C H2 ) 20 (C
H 2 ) 15S H and C F3 (C F2 ) 9 (C H2 ) 2 S H or such adsorption liquids which can be obtained by adding, for instance, C H 3 ( C H 2 ) 19 S H to chlorosilane-based or fluorotitanate-based or fluorothiol-based surface active materials.
205725û
While the above examples are primarily concerned with tempered glass substrates, the invention is applicable to all kinds of glass which require improved water- and oil-repelling properties such as window glass or mirror used for buildings or vehicles, trains and airplanes or glass vessels or lenses.
With a glass substrate having surface irregularities on the order of microns, the anti-contaminating property is slightly inferior. However, the water wetting angleia from 145 to 155 degrees, and the water- and oil-repelling properties and anti-fogging property are improved.
The water-repelling, oil-repelling, anti-fogging, anti-contaminating film coating according to the invention can be formed not only on glass substrates, but the invention is applicable to substrates made of metals, semiconductors, plastics, etc. as well.
As has been described in the foregoing, the water-repelling, oil-repelling, anti-fogging, anti-contaminating film coating according to the invention comprises a monomolecular film formed on a substrate surface and having minimal surface irregularities which are generally confined to irregularities at the molecular level. Thus, it is possible to form a higher density organic thin film coating, which is substantially free of pin holes, has a uniform thickness, is very thin and has excellent water- and oil-repelling properties. That is, with the treatment according to the invention, it is possible to obtain a highly durable surface treatment and prevent the contamination, fogging and wetting of substrate surfaces.
As has been shown, the invention is greatly beneficial to industry.
The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiment is to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description and all changes which come within the meaning and range of equivalency of the claims are intended to be embraced therein.
film is formed, is hydrophilic or has been made hydrophilic.
Another aspect of this invention is to provide a process of manufacturing an adsorbed monomolecular film by a chemical adsorption process comprising the steps of:
preparing a coating composition which comprises a blend surface active material in a non-aqueous solvent, the blend surface active material comprising two molecules differing in molecular chain length and each having at one end a halosilane or alkoxysilane group and at the other end a fluorinated alkyl ~0 group; and contacting the coating composition with a substrate having at a surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane, and causing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming a monomolecular film on the substrate surface.
One embodiment of the process, comprises the steps of:
preparing a coating composition constituted by a surface active material in a non-aqueous solvent, the surface active material having at one end a halosilane or alkoxysilane group, and contacting the coating composition with a substrate having at the surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane, and causing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming an inner layer on the substrate surface;
adding a hydroxyl group (-OH), an amino group (-NH2), or an imino group (-NH) on the inner layer surface; and Z ~ ~ 7 ~ 5 0 preparing a coating composition which comprises a blend surface active material in a non-aqueous solvent, the blend surface active material comprising two molecules differing in molecular chain length and each having at one end a halosilane or alkoxysilane group and at the other end a fluorinated alkyl group, and contacting the coating composition with the inner layer having at the surface thereof the hydroxyl, amino or imino group (i.e. an active hydrogen capable of reacting with the halosilane or alkoxysilane), thereby laminating a monomolecular film on the inner layer surface.
The adsorbed monomolecular film is chemically bonded by a covalent bond each containing a -Si- group to the surface of a substrate either directly or via an inner layer and the adsorbed monomolecular film is constituted by at least two different molecules having different molecular lengths.
It is preferable in this invention that the adsorbed monomolecular film is formed as a lamination on the inner layer and the inner layer has a substantially uniform ~ ~7 250 thickness.
It is preferable in this invention that the inner layer is directly bonded by covalent bonds each having a -Si- group to the substrate surface and is also bonded by covalent bonds each having a -Si- group at the outer adsorbed monomolecular film.
It is preferable in this invention that the adsorbed monomolecular film has molecular surface irregularities to a molecular level extent.
It is preferable in this invention that the adsorbed monomolecular film is either water-repelling, oil-repelling, anti-fogging property or an anti-contaminating.
It is preferable in this invention that the adsorbed monomolecular film is comprises at least one monomolecular compound selected from the group consisting of the formula [I]
[I] F (C F2 ) m (C H2 ) n S i ( R q ) (~3-q ) where m represents an integer ranging from 1 to 15, n represents an integer ranging from O to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from O
to 2, and R represents an alkyl group or an alkoxyl group.
[II] F (C F 2 ) s (C H2 ) t A ( C H 2 ) p S i (R q ) ( 03-q ) where s represents an integer ranging from 1 to 8, t represents an integer ranging from O to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from O to 2, A represents a member of a group consisting of an oxy group(-O-), a carbonyl group (~C=O), a carboxyl-ester group (-COO-) and dimethylsilylene group (- S i (C H 3 ) 2 -) and R represents an alkyl group or an alkoxyl group.
It is preferable in this invention that the molecules of the blend surface active material have an alkyl fluoride group.
It is preferable in this invention that the molecules of the blend surface active material has at one end a trifluoromethyl group (-CF3 ) and the other end a chlorosilane group (-SiCl).
It is preferable in this invention that the blend surface active material contains a silane surface active material represented by the formula;
F (C F2 ) m (C H 2 ) n S i (R q ) (X3-q ) where m represents an integer ranging from 1 to 15, n represents an integer ranging from O to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from O
to 2, and R represents an alkyl group or an alkoxyl group, X
represents a halogen atom or an alkoxyl group, and by the formula;
F (C F2 ) s (C H2 ) t A (C H2 ) p S i (Rq ) (X3_q ) where s represents an integer ranging from 1 to 8, t 20~250 represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from O to 2, X represents a halogen atom or an alkoxyl group, R represents an alkyl group or an alkoxyl group, A represents a member of a group consisting of an oxy group (-O-), a carbonyl group ( ~C=O), a carboxyl-ester group (-COO-) and dimethylsilylene group ( - S i ( C H3 ) 2 -) -BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a schematic sectional view, enlarged inscale to the molecular level showing an inner layer having vinyl groups on the surface of a substrate as described in Example 1 of this invention.
Figure 2 is a schematic sectional view, enlarged in scale to the molecular level showing the inner layer forming hydroxy groups on the surface of a substrate as described in Example 1 of this invention.
Figure 3 is a schematic sectional view, enlarged in scale to the molecular level showing the inner layer forming amino groups on the surface of a substrate as described in Example 1 of this invention.
Figure 4 is a schematic sectional view, enlarged in scale to the molecular level showing the laminating monomolecular film on the inner layer surface of a substrate as described in Example 1 of this invention.
~ ~ 5 ~ ~ S ~
Figure 5 is a schematic sectional view, enlarged in scale to the molecular level showing the monomolecular film on a substrate as described in Example 1 of this invention.
Figure 6 is a schematic sectional view, enlarged in scale to the molecular level showing the monomolecular film on the surface of nylon-6,6 substrate as described in Example 2 of this invention.
DETAILED DESCRIPTION OF THE lNV~L. ~lON
According to the invention, the above problems are solved by a water-repelling, oil-repelling, anti-fogging, and anti-contaminating film comprising a monomolecular film formed on a substrate surface and containing a fluorinated alkyl group, the monomolecular film having minimal surface irregularities wherein the irregularities are generally confined to the molecular level.
By incorporating onto the substrate surface a monomolecular film which contains a plurality of different fluorinated alkyl groups having different molecular lengths, a coating in the form of a monomolecular film can be obtained which has minimal surface irregularities. Typically, such surface irregularities are confined to the molecular level.
Because the surface has minimal irregularities and the molecules constituting the monomolecular film contain fluorine, the area of contact between water drops and the film surface can be reduced. Thus the film itself can have a very high water-repelling property. The film similarly repels oil drops, and therfore provides an improved oil-repelling property. With both these effects, the anti-fogging and anti-contaminating properties can also be improved.
The substrate to be used according to the invention is of such materials as pure metals, e.g., aluminum, copper and iron, alloys or like composite materials, semiconductors, fiber, cloth, fabric, fur, leather, wood e.g., silicon and germanium, glass and plastics. According to the invention, a hydrophilic substrate is used. Where the substrate is made of a common base metal or a semiconductor, it is made hydrophilic by a natural oxide film formed on its surface. In case of a relatively non-hydrophilic substrate such as a plastic substrate, a hydrophilic property is imparted by, for instance, a corona treatment, plasma treatment or an ion beam irradiation. Furthermore, with a relatively non-hydrophilic substrate, it is recommended to form a monomolecular film in advance of a surface active material having unsaturated carbon-carbon bond groups by using such means as a Langmuir-Blodgett's technique (hereinafter referred to as LB process) or a chemical adsorption process and then forcibly rendering the film hydrophilic by such means as causing breakage of the unsaturated bonds in an atmosphere containing oxygen, _ g _ .~.. . . .. . . .. . .
nitrogen, etc. This is preferred because many hydrophilic group~ are formed on the surface of the substrate, and a high concentration of monomolecular film can be obtained at the surface of the substrate. As a reagent for rendering the substrate surface hydrophilic the following compounds may be used C H2 = C H - ( C H 2 ) n - S i C 13 and C H 2 = C H - ( C H 2 ) n - C O O H (where n represents an integer desirably about 10 to 20). The monomolecular film may be formed by ordinary means such as the LB process or the chemical adsorption process. Unsaturated bonds may be broken by ordinary means such as treatment with an electron beam, X-rays, gamma-rays, ultraviolet rays or an ion beam, plasma or corona treatment.
However, plastics having _NH groups such as polyamide or polyurethane substrates are not necessary in a surface oxygen treatment. Because as _NH groups have active hydrogen, it is relatively easy to reduce the groups by initiating the dehydrochloric acid reaction using the chlorosilyl groups of surface active material.
The film coating according to the invention is formed by utilizing a very thin monomolecular film, and therefore the initial surface state of the substrate may be maintained as such.
The monomolecular film according to the invention may 20~7250 be formed on the substrate either directly or via a protective film or the like. Particularly, the monomolecular film according to the invention is suitably formed via such a functional film as a protective film, an anti-reflection film or an infrared-absorbing film. By doing so, it is possible to maintain high anti-reflecting or infrared-adsorbing properties for long time and also obtain a protective or like functional effect in addition to the nater-repelling, oil-repelling, anti-fogging and anti-contaminating effects owing to the monomolecular film.
According to the invention, on a substrate surface is formed either directly or via a given film such as a protective film a water-repelling, oil-repelling, anti-fogging anti-contaminating film in the form of a monomolecular film, which contains a plurality of different kinds of fluorine (F) containing group having different molecular lengths, the surface of which is predominantly confined to molecular irregularities. The monomolecular film may be formed by the LB process, the chemical adsorption process or any other usual process. In the chemical adsorption process, the reagent is adsorbed via chemical bonds to the substrate, and therefore this process is preferred for maintain highly close contact with the substrate. Moreover high mechanical strength of the monomolecular film can be obtained.
~i 7 ~ ~ ~
Where the LB process is used to form the monomolecular film according to the invention, a carboxylic acid (-COOH), a carboxylic acid salt, an ester, a trialkoxysilane, a trihydrosilane, etc. having a fluorinated alkyl group in a molecule may be used.
Where the chemical adsorption process is used to form the monomolecular film according to the invention, preferably used are fluorochlorosilane-based surface active materials containing a fluorinated alkyl group and a chlorosilyl group, fluorotitanium-based surface active materials containing a fluorinated alkyl group and a titanate group, fluorothiol surface active materials having a fluorinated alkyl group and a thiol group.
As for the fluororchlorosilane-based surface active materials to be used according to the invention, they are suitably those represented such as in the formulas [A] and [B]. These fluorochlorosilane-based surface active materials are suitable because they are readily available and have pronounced water-repelling, oil-repelling, anti-fogging and anti-contaminating effects.
They are suitably those represented by the formulas;
CF3(cH2)2si(cH3)2(cH2)l5sicl3l CF3(cF2)3(cH2)2si(cH3)2(cH2)9sic13, C F 3 C H 2 ~ (C H 2 ) 15s i C l3 C F 3 C O O (C H 2 ) 15s i C 13 , C F 3 (C F 2 ) 9 (C H 2 ) 2 S i C l 3 , C F 3 (C F 2 ) 7 (C H 2 ) 2 S i C l 3 , and C F 3 (C F 2 ) 5 (C H 2 ) 2 S i C l 3 -As the fluorotitanium-based or fluorothiol-based surface active materials for producing the monomolecular film according to the invention by the chemical adsorption process, those compounds obtained by substituting titanate or thiol for the chlorosilyl group of the above chlorosilane-based surface active material may be used.
Where an alkoxysilane-based surface acive material is used, adsorption is effected with an alcohol removal reaction when forming a chemically adsorbed monomolecular film. When a fluorothiol-based surface active material is used, adsorption is effected with a hydrous reaction. These surface active materials are therefore preferred to surface active materials having chlorosilyl groups, because they do not cause damage to even metal substrates.
The invention can widely be applied to the following uses. Materials made of metal, ceramic or plastic, glass, wood, stone, fiber, cloth, fabric, fur, leather etc. are applicable to the substrate. The surface of the substrate can also be coated with paint or the like.
2057~50 Examples of cutlery: a kitchen knife, scissors, a knife, a cutter, a graver, a razor, hair clippers, a saw, a plane, a chisel, a gimlet, a badkin, bite (cutting tools), a edge of a drill, a edge of a mixer, a juicer, a blade of a mill, a blade of a lawn mower, a punch, a straw cutter, a staple of a stapler, a can opener or a surgical knife and the like.
Examples of needles: an acupuncture, a needle, a sewing needle, a matting needle, an injection needle, a surgical needle, a safety pin and the like.
Examples of products in pottery (ceramics) industry:
products made of pottery, glass, ceramics or an enameled products. For example, sanitary potteries ( a chamber pot, a wash-bowl, a bathtub, etc.), tableware ( a rice-bowl teacup, a dish (plate), a bowl, a teacup, a glass, a bottle, a coffee-pot (siphon), a pan, an earthenware mortar, (a cup and the like), vases ( a flower bowl, a flowerpot, a bud vase and the like), water tanks (a breeding cistern, an aquarium water tank and the like), chemical experiment appliances ( a beaker, a reactor vessel, a test tube, a flask, a laboratory dish, condenser, a mixing rod, a stirrer, a mortar, a bat, a syringe, etc.) a roof tile, enameled ware, an enameled washbowl, an enameled pan and the like.
Examples of molding parts: dies for press molding, dies for cast molding, dies for injection molding, dies for , i, , ,. ,.. " , . . .. . . . .
transfer molding, dies for compression molding, dies for transfer molding, dies for inflation molding, dies for vacuum molding, dies for blow forming, dies for extrusion molding, dies for fiber spinning, a calendar processing roll and the like.
Examples of forming molds for food: cake, cookies, bread-baking, chocolate, jelly, ice cream, an oven ware, an ice tray and the like.
Examples of cookware: kitchen utensils (a pan and a pot), a kettle, a pot, a frying-pan, a hot plate, a gridiron net, a takoyaki plate and the like.
Examples of resin(s): a polyolefin such as a polypropylene and polyethylene, a polyvinylchloride plastic, a polyamide, a polyimide, a polyamideimide, a polyester, an aromatic polyester, a polycarbonate, a polystyrene, a polysulfide, a polysulfone, a polyethersulfone, a polyphenylenesulfide, a phenolic resin, a furan resin, a urea resin, a epoxy resin, a polyurethane, a silicon resin, an ABS
resin, a methacrylic resin, an acrylate resin, a polyacetal, a polyphenylene oxide, a polymethylpentene, a melamine resin, an alkyd resin, an unsaturated polyester cured resin and the like.
Examples of rubber(s): a styrene-butadiene rubber, a butyl rubber, a nitril rubber, a chloroprene rubber, a , ~ .. .. ..
2057~0 polyurethane rubber, a silicon rubber and the like.
Examples of household electric appliances: a refrigerator, a freezer, an air conditioner, a juicer, a mixer, a blade of an electric fan, a lighting apparatus, a dial plate, a dryer for a perm and the like.
Examples of sporting goods: skis, a fishing rod, a pole for the pole vault, a boat, a yacht, a surfboard, a fishing line, a float and the like.
Examples applying to vehicle parts:
(1) ABS resin: a lamp cover, an installment pannel, trimming parts, a protector for a motorcycle.
(2) Cellulose plastic: a car mark, a steering wheel (3) FRP (fiber reinforced plastics): a bumper, an engine cover (jacket) (4) Phenolic resin: a brake (5) Polyacetal: wiper gear, a gas valve (6) Polyamide: a radiator fan (7) Polyarylate (polycondensation polymerization by bisphenol A and pseudo phthalic acid): a direction indicator lamp (or lense), a cowl board lense, a relay case (8) Polybutylene terephthalate (PBT): a rear end, a front fender (9) Poly amino-bismaleimide : engine parts, a gear box, a wheel, a suspension drive system 20~72~0 (10) Methacrylate resin: a lamp cover lens, a meter pannel and its cover, a center mark (11) Polypropylene: a bumper (12) Polyphenylen oxide : a radiator grille, a wheel cap (13) polyurethane: a bumper, a fender, an installment pannel, a fan (14) Unsaturated polyester resin: a body, a fuel tank, a heater housing, a meter pannel.
Examples of office supplies: a desk, a chair, a bookshelf, a rack, a telephone stand table, a rule (measure), a drawing instrument and the like.
Examples of building materials: materials for a roof, and outer wall and interiors. Roof materials such as brick, slate and tin (a galvanized iron sheet) and the like. Outer wall materials such as wood (including processed manufactured wood), mortar, concrete, ceramic sizing, metalic sizing, brick, stone, plastic and metal like an aluminium. Interior materials such as wood (including processed wood), metal like an aluminium, plastic, a paper, fiber and the like.
Examples of building stones: granite, marble and others for use as a building,a building material, an architecture, an ornament, a bath, a grave stone, a monument, a gatepost, a stone wall, a paving stone and the like.
Examples of the others: a high resisting voltage insulator such as a thermos bottle, a power supplying insulator for a vacuum system machinery or a spark plug, which has high water-repellent, oil-repellent, anti-fogging and anti-contamination effects.
Specific examples of the process of chemical adsorption of a water-repelling oil-repelling anti-fogging, anti-contaminating film coating according to the invention will now be described with reference to Figures 1 to 5.
Example 1 As solution containing 80 % wt n-hexadecane, 12 % wt carbon tetrachloride and 8 % wt chloroform was prepared by using C H2 = C H - (C H2 ) 16- S i C l3 as a silane surface active material and dissolving the same to a concentration of 3 x 10 3 to 5 x 10 2 mol, and a tempered glass substrate 1, as shown in Figure 1, was dipped into this solution and held at room temperature for one hour. Since the surface of the substrate 1 contained hydroxyl groups, a reaction between the chlorosilyl groups of the chlorosilane-based surface active material and the hydroxyl groups, thus forming on the surface bonds represented such as the formula [1] .
, ~ ~ ~ 7 ~ ~ ~
CH2= CH -(CH2)l6-SiCl3 + (-OH) CH2= CH -(CH2)l6-lSi-O - + HC1 The tempered glass 1 was then washed by Freon 113*
to remove the material remaining on the surface without reaction, followed by washing with water or exposing to air to react with moisture in the air. The -SiCl group was changed to a -SiOH group as in formula [2].
CH2=CH--(CH2)l6--ISi--O-- + 2H20 OH
CH2=CH -(CH2)16-~i-O - + 2HC1 OH
Fonnu~[2 ]
Each silanol group (-SiOH) was then dehydrated and crosslinked to form a siloxan bond (-SiO-) as in formula [3].
* Trade-mark ~ 73466-15 O H
I
n CH2 = CH-- (CH2 ) 16--S i --O--I
O H
I
~n C H2 = C H-- (C H2 ) 16--S i --O-- + n H2 ~
I
o - Formula [3]
By the consecutive reaction, a single adsorbed monomolecular film 3 having vinyl (CH2 =CH-) groups 2 was formed to a thickness of about 2.5 nm such that it was chemically bonded (i. e., covalently bonded) to a protective film via oxygen atoms.
This glass substrate 1 was irradiated with about 3 Mrad. of X-rays in an atmosphere containing oxygen and also in an atmosphere containing nitrogen. Where the substrate 1 was irradiated in the oxygen-containing atmosphere, a monomolecular film 3' (inner layer), as shown in Figure 2, was obtained, which contained hydroxyl (-OH) groups 4 added to the vinyl groups 2. Where the irradiation was done in the nitrogen-containing atmosphere, a monomolecular film 3" (inner layer) was obtained, as shown in Figure 3, which contained , . . ~.
amino groups (-NH2 ) 5 added to the vinyl groups 2. The addition of the functional groups, i.e., the -OH, -NH2 and -NH groups, to the vinyl groups, was confirmed as a result of a FTIR analysis.
Subsequent to the addition of -OH groups, a solution containing 80 % wt n-hexadecane, 12 % wt carbon tetrachloride and 8 % wt chloroform was prepared by using C F3 (C F 2 ) 7 (C H 2 ) 2 S i C 13 and C F 3 C H 2 ~ (C H2 ) 15S i C l 3 as respective chemical adsorption materials and dissolving these reagents to respective concentrations of about 2 x 10 3 to 5 x 10 2 Mol and at a mixing ratio of 3 : 1 to 1 : 3, and the glass substrate 1 forming the monomolecular film 3', as shown in Figure 2, was dipped into the solution and held for one hour. Since -OH groups 4 were exposed at the surface of the substrate 1, the chlorosilic groups of the chlorosilane-based surface active material having fluorine and -OH groups 4 were reacted. Thus, bonds represented by formulas [4] and [5]
were produced on the surface substantially at the above mixing ratio. This reaction proceeded substantially the same as above in formulas [1] to [3].
... ~ .. . ~ ...... .... ~
2~57250 C F3 (C F 2 ) 7 (C H 2 ) 2 S i ~ - Formula [4]
O-O-I
C F3 C H2 0 (C H2 ) 15 S i O - Formula [5]
I
Thus, a high concentration monomolecular lamination film 7 can be obtained on the surface of the glass substrate 1, as shonn in Figure 4. The film 7 includes an adsorbed monomolecular film 6 which has a fluorine group and surface irregularities which are generally molecular irregularities.
The adsorbed monomolecular film is chemically bonded (i. e., covalently bonded) to the inner layer 3 ' .
The water wetting angle measured at the surface of the adsorbed monomolecular film 6 was from 140 to 150 degrees.
The measured value showed an improvement by about 20 to 30 degrees from 120 degrees, which was obtained by using only a single kind of fluorosilane-based surface active material.
The resultant glass therefore can be used to obtain a wiper-free vehicle window glass and to prevent fogging on, for ~ ~7 ~
instance, glass lens surfaces.
These effects can be obtained by forming a monomolecular film containing fluorinated alkyl groups on the outermost substrate surface wherein the fluorinated alkyl groups have different molecular lengths such as formulas 4 and 5, with the surface being substantially pin hole free.
Where no intermediate monomolecular film is necessary between the surface water-repelling, oil-repelling film and the glass substrate, a singularly adsorbed monomolecular film 8 containing fluorine may be formed on a glass surface directly, as shown in Figure 5, by using a chlorosilane-based surface active material having fluorine and a mixing ratio of, for example, 1:1. Such a glass was shown to have sufficient water- and oil-repelling properties.
Where a plurality of intermediate monomolecular films are necessary, the steps of chemical adsorption and subsequent radiation irradiation are repeated a number of times corresponding to the necessary laminated film number.
For example CH2= CH(CH2)16-SiCl3 and a plurality of different chlorosilane-based surface active materials having fluorinated alkyl groups with different molecular lengths can be adsorbed as adsorption reagents. By doing so, a water-repelling, oil-repelling film having a single fluorine-containing adsorbed monomolecular film can be formed on a ~A ~
f~ 73466-15 glass surface via a number of intermediate laminated monomolecular films.
In the above example, as to the reagent for forming the outermost surface adsorbed monomolecular film containing fluorine and dimethylsilylene or oxygen atom or a carboxy ester the following can be used;
CF3(cH2)2si(cH3)2(cH2)l5sicl3/
F(CF2)4(CH2)2Si(CH3)2(CH2)gSiCl3 CF3COO(CH2)1sSicl3 CF3(CF2)g(CH2)2sicl3 CF3(CF2)5(CH2)2sicl3 Example 2 A chemically adsorbing solution was prepared by using Freon 113 , CF3(CF2)7(CF2)2SiCl3 and CF3CH2 O(CH2)15SiCl3 as silane surface active materials. The surface active materials were each dissolved to a concentration of 1 wt. A nylon-6,6 substrate was dipped into this solution and held at room temperature for one hour. Since the surface of the nylon-6,6 substrate contained imino groups (=NH), a reaction between the chlorosilyl groups of the chlorosilane-based surface active material and the imino groups formed surface bonds as represented in the formulas [6] and [7].
This reaction proceeded substantially as in formulas [1] to [3].
* Trade-mark r~
CF3(cF2)7(cH2)2ri- N-- Fo~n~a[6]
CF3CH2O(CH2)1s~i- I--Fonn~a[7]
Thus, a high concentration monomolecular film 9 can be obtained on the surface of the nylon-6,6 substrate 10, as shown in Figure 6. The adsorbed monomolecular film 9 has a fluorine group and surface irregularities which are generally molecular surface irregularities. The adsorbed monomolecular film is chemically bonded (i.e., covalently bonded) to the substrate 10.
The water wetting angle measured at the surface of the monomolecular adsorbed film 9 was from 140 to 150 degrees.
A water-repelling, oil-repelling film having a single fluorine-containing monomolecular adsorbed film was formed on the substrate 10.
Example 3 This example, like Example 1, concerns the formation ~ ~ ~ 7 ~
of the water-repelling, oil-repelling, anti-fogging, anti-contaminating film coating by the LB process using a tempered glass substrate.
A blend surface active material was obtained by mixing two different surface active materials, i.e., CF3(CF2)7(CH2)2COOH and CF3CH2O(CH2)15COOH at a mixing ratio of 1:1, and 10 mg was dissolved in 100 g of chloroform. The solution was then quietly developed on the water surface.
A tempered glass substrate as in Example 1 was then dipped at a speed of 1 cm/min. under a pressure of 50 mN/m and then raised.
As a result, a film coating having molecular surface irregularities and containing fluorinated alkyl groups was formed on the tempered glass substrate. This film coating had the same water-repelling property as the film obtained in Example 1.
The water-repelling effect obtained in this example is attributable to the fact that like Example 1 the monomolecular film containing fluorinated alkyl groups is formed as the outermost surface layer on the substrate. The fluorinated alkyl groups are characterized by having different constituent molecules, different molecular lengths.
Any of the above examples can also use two different surface active materials in combination. By using three or more different reagents, a monomolecular film having three or more different reagents can be obtained. Such a monomolecular film has similar water- and oil-repelling effects.
Where a glass surface has a protective film or anti-reflection film such as metal or a metal oxide film, or an infrared-adsorbing film such as color formed infrared film, a chemically adsorbed film can be formed by appropriately controlling the adsorption time so long as the surface has hydrophilic groups such as hydroxy groups.
Adsorbed films can be obtained under similar conditions by using, in lieu of the above chlorosilane-based surface active materials, fluorotitanate-based surface active materials such as a combination Of F ( C F 2 ) 8 S i (C H3 ) 2 (C H2 ) 9 T i 0 C H (C H3 ) 2 and C F3 (C F2 ) 9 (C H2 ) 2 T i 0 C H (C H3 ) 2, or F (C F2 ) 4 (C H2 ) 2 S i (CH3 ) 2 (CH2 ) 9 T i C 13, CF3 (CF2 ) 5 ( C H2 ) 2 S i T i 3, or a fluorothiol-based surface active material such as a combination of F (C F 2 ) 4 (C H2 ) 20 (C
H 2 ) 15S H and C F3 (C F2 ) 9 (C H2 ) 2 S H or such adsorption liquids which can be obtained by adding, for instance, C H 3 ( C H 2 ) 19 S H to chlorosilane-based or fluorotitanate-based or fluorothiol-based surface active materials.
205725û
While the above examples are primarily concerned with tempered glass substrates, the invention is applicable to all kinds of glass which require improved water- and oil-repelling properties such as window glass or mirror used for buildings or vehicles, trains and airplanes or glass vessels or lenses.
With a glass substrate having surface irregularities on the order of microns, the anti-contaminating property is slightly inferior. However, the water wetting angleia from 145 to 155 degrees, and the water- and oil-repelling properties and anti-fogging property are improved.
The water-repelling, oil-repelling, anti-fogging, anti-contaminating film coating according to the invention can be formed not only on glass substrates, but the invention is applicable to substrates made of metals, semiconductors, plastics, etc. as well.
As has been described in the foregoing, the water-repelling, oil-repelling, anti-fogging, anti-contaminating film coating according to the invention comprises a monomolecular film formed on a substrate surface and having minimal surface irregularities which are generally confined to irregularities at the molecular level. Thus, it is possible to form a higher density organic thin film coating, which is substantially free of pin holes, has a uniform thickness, is very thin and has excellent water- and oil-repelling properties. That is, with the treatment according to the invention, it is possible to obtain a highly durable surface treatment and prevent the contamination, fogging and wetting of substrate surfaces.
As has been shown, the invention is greatly beneficial to industry.
The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiment is to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description and all changes which come within the meaning and range of equivalency of the claims are intended to be embraced therein.
Claims (10)
1. A monomolecular film of at least two different molecules having at one end fluorinated alkyl groups with different molecular lengths and being at the outer end covalently bonded through an -Si- bond to a surface of a substrate either directly or via an inner layer, wherein:
the monomolecular film has surface irregularities which are confined to a molecular level, and the surface of the substrate, before the monomolecular film is formed, is hydrophilic or has been made hydrophilic.
the monomolecular film has surface irregularities which are confined to a molecular level, and the surface of the substrate, before the monomolecular film is formed, is hydrophilic or has been made hydrophilic.
2. The monomolecular film according to claim 1, which is formed as a lamination on an inner layer and the inner layer is substantially uniform in thickness.
3. The monomolecular film according to claim 1 or 2, wherein the inner layer is directly bonded by covalent bonds to the substrate surface.
4. The monomolecular film according to claim 1, 2 or 3 which is water-repelling, oil-repelling, anti-fogging or anti-contaminating.
5. The monomolecular film according to any one of claims 1 to 4, wherein the different molecules are selected from the group consisting of:
F(CF2)m-(CH2)n-Si(-Rq)(-0-)3q (I) (where m represents an integer ranging from 1 to 15, n represents an integer ranging from 0 to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from 0 to 2, and R represents an alkyl group or an alkoxy group), and F(CF2)s-(CH2)t-A-(CH2)q-Si(-Rq)(-O-)3-q (II) (where s represents an integer ranging from 1 to 8, t represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from 0 to 2, A represents a member of a group consisting of an oxy group (-O-), a carbonyl group (-CO-), a carboxyl-ester group (-COO-) and dimethylsilane group (Si(CH3)2-), and R
represents an alkyl group or an alkoxy group).
F(CF2)m-(CH2)n-Si(-Rq)(-0-)3q (I) (where m represents an integer ranging from 1 to 15, n represents an integer ranging from 0 to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from 0 to 2, and R represents an alkyl group or an alkoxy group), and F(CF2)s-(CH2)t-A-(CH2)q-Si(-Rq)(-O-)3-q (II) (where s represents an integer ranging from 1 to 8, t represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from 0 to 2, A represents a member of a group consisting of an oxy group (-O-), a carbonyl group (-CO-), a carboxyl-ester group (-COO-) and dimethylsilane group (Si(CH3)2-), and R
represents an alkyl group or an alkoxy group).
6. A process of manufacturing an adsorbed monomolecular film by a chemical adsorption process comprising the steps of:
preparing a coating composition comprising a blend surface active material in a non-aqueous solvent, the blend surface active material comprising at least two molecules different in molecular chain length and each having at one end a halosilane or alkoxysilane group and at the other end a fluorinated alkyl group; and contacting the coating composition with a substrate having at a surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane group, and allowing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming a monomolecular film on the substrate surface.
preparing a coating composition comprising a blend surface active material in a non-aqueous solvent, the blend surface active material comprising at least two molecules different in molecular chain length and each having at one end a halosilane or alkoxysilane group and at the other end a fluorinated alkyl group; and contacting the coating composition with a substrate having at a surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane group, and allowing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming a monomolecular film on the substrate surface.
7. The process according to claim 6, wherein each molecule of the blend surface active material has at one end a trifluoromethyl group (-CH3) and at another end a chlorosilane group (-SiCl).
8. The process according to claim 6, wherein the blend surface active material comprises a silane surface active material represented by the formula;
F(CF2)m-(CH2)n-Si(-R)q(-X)3-q (where m represents an integer ranging from 1 to 15, n represents an integer ranging from 0 to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from 0 to 2, R represents an alkyl group or alkoxyl group, and X
represents a halogen atom or an alkoxyl group);
or the formula:
F(cF2)s-(cH2)t-A-(cH2)p-si(-R)q(-x)3 q (where s represents an integer from 1 to 8, t represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from 0 to 2, R
represents an alkyl or an alkoxyl group, X represents a halogen atom or an alkoxyl group, and A is a group selected from the group consisting of an oxy group (-O-), a carbonyl group (-CO-), a carboxylester group (-COO-) and a dimethylsilane group (-Si(CH2)2-).
F(CF2)m-(CH2)n-Si(-R)q(-X)3-q (where m represents an integer ranging from 1 to 15, n represents an integer ranging from 0 to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from 0 to 2, R represents an alkyl group or alkoxyl group, and X
represents a halogen atom or an alkoxyl group);
or the formula:
F(cF2)s-(cH2)t-A-(cH2)p-si(-R)q(-x)3 q (where s represents an integer from 1 to 8, t represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from 0 to 2, R
represents an alkyl or an alkoxyl group, X represents a halogen atom or an alkoxyl group, and A is a group selected from the group consisting of an oxy group (-O-), a carbonyl group (-CO-), a carboxylester group (-COO-) and a dimethylsilane group (-Si(CH2)2-).
9. A process of manufacturing an adsorbed monomolecular film by a chemical adsorption process comprising the steps of:
preparing a coating composition comprising a surface active material in a non-aqueous solvent, the surface active material having at one end a halosilane or alkoxysilane group, contacting the coating composition with a substrate having at the surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane group and allowing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming an inner layer on the substrate surface;
adding a hydroxyl group (-OH), an amino group (-NH2), or an imino group (-NH) on the inner layer surface;
preparing a coating composition comprising a blend surface active material in a non-aqueous solvent, the blend surface active material comprising at least two molecules different in molecular chain length and each having at one end a halosilane or alkoxysilane group, and at the other end a fluorinated alkyl group, and contacting the coating composition with the inner layer having at the surface thereof and allowing the hydroxyl, amino or imino group to react with the halosilane or alkoxysilane group, thereby laminating a monomolecular film onto the inner layer surface.
preparing a coating composition comprising a surface active material in a non-aqueous solvent, the surface active material having at one end a halosilane or alkoxysilane group, contacting the coating composition with a substrate having at the surface thereof an active hydrogen capable of reacting with the halosilane or alkoxysilane group and allowing the active hydrogen to react with the halosilane or alkoxysilane group, thereby forming an inner layer on the substrate surface;
adding a hydroxyl group (-OH), an amino group (-NH2), or an imino group (-NH) on the inner layer surface;
preparing a coating composition comprising a blend surface active material in a non-aqueous solvent, the blend surface active material comprising at least two molecules different in molecular chain length and each having at one end a halosilane or alkoxysilane group, and at the other end a fluorinated alkyl group, and contacting the coating composition with the inner layer having at the surface thereof and allowing the hydroxyl, amino or imino group to react with the halosilane or alkoxysilane group, thereby laminating a monomolecular film onto the inner layer surface.
10. The process according to claim 9, wherein the blend surface active material comprises a silane surface active material represented by the formula;
F(CF2)m-(CH2)n-Si(-R)q(-X)3-q (where m represents an integer ranging from 1 to 15, n represents an integer ranging from 0 to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from 0 to 2, R represents an alkyl group or alkoxyl group, and X
represents a halogen atom or an alkoxyl group);
or the formula:
F(cF2)S-(CH2)t-A-(CH2)p-Si(-R)q(-X)3-q (where s represents an integer from 1 to 8, t represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from 0 to 2, R
represents an alkyl or an alkoxyl group, X represents a halogen atom or an alkoxyl group, and A is a group selected from the group consisting of an oxy group (-O-), a carbonyl group (-CO-), a carboxylester group (-COO-) and a dimethylsilane group (-Si(CH2)2-).
F(CF2)m-(CH2)n-Si(-R)q(-X)3-q (where m represents an integer ranging from 1 to 15, n represents an integer ranging from 0 to 15, the sum of m and n ranges from 10 to 30, q represents an integer ranging from 0 to 2, R represents an alkyl group or alkoxyl group, and X
represents a halogen atom or an alkoxyl group);
or the formula:
F(cF2)S-(CH2)t-A-(CH2)p-Si(-R)q(-X)3-q (where s represents an integer from 1 to 8, t represents an integer ranging from 0 to 2, p represents an integer ranging from 5 to 25, q represents an integer ranging from 0 to 2, R
represents an alkyl or an alkoxyl group, X represents a halogen atom or an alkoxyl group, and A is a group selected from the group consisting of an oxy group (-O-), a carbonyl group (-CO-), a carboxylester group (-COO-) and a dimethylsilane group (-Si(CH2)2-).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP400981/1990 | 1990-12-10 | ||
| JP40098190 | 1990-12-10 |
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|---|---|
| CA2057250A1 CA2057250A1 (en) | 1992-06-11 |
| CA2057250C true CA2057250C (en) | 1999-08-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002057250A Expired - Fee Related CA2057250C (en) | 1990-12-10 | 1991-12-09 | Adsorbed monomolecular film and method of manufacturing the same |
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| Country | Link |
|---|---|
| US (2) | US5225274A (en) |
| EP (1) | EP0491251B1 (en) |
| JP (1) | JP2637869B2 (en) |
| KR (1) | KR960006088B1 (en) |
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| DE102011085428A1 (en) | 2011-10-28 | 2013-05-02 | Schott Ag | shelf |
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| WO2013140576A1 (en) * | 2012-03-22 | 2013-09-26 | 日本特殊塗料株式会社 | Frost preventive coating composition |
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| US4539061A (en) * | 1983-09-07 | 1985-09-03 | Yeda Research And Development Co., Ltd. | Process for the production of built-up films by the stepwise adsorption of individual monolayers |
| JPS6116910A (en) * | 1984-07-03 | 1986-01-24 | Hitachi Cable Ltd | Fluororesin composition crosslinkable with radiation |
| JPS61237636A (en) * | 1985-04-15 | 1986-10-22 | 大同鋼板株式会社 | Coated steel plate |
| US4992300A (en) * | 1988-05-24 | 1991-02-12 | Matsushita Electric Industrial Co., Ltd. | Manufacturing method for a recording medium or a recording head |
| JPH0761428B2 (en) * | 1989-03-09 | 1995-07-05 | 松下電器産業株式会社 | Permselective membrane and method for producing the same |
| US5039555A (en) * | 1988-10-12 | 1991-08-13 | Matsushita Electric Industrial Co., Ltd. | Method of preparing lubricant for recording media |
| CA1329341C (en) * | 1988-10-19 | 1994-05-10 | Rosemary Bridget Albinson | Method of forming adherent fluorosilane layer on a substrate and ink jet recording head containing such a layer |
| EP0385656B1 (en) * | 1989-02-27 | 1995-05-10 | Matsushita Electric Industrial Co., Ltd. | A process for the production of a highly-orientated ultralong conjugated polymer |
| JP2637869B2 (en) * | 1990-12-10 | 1997-08-06 | 松下電器産業株式会社 | Adsorbed monomolecular film and method for producing the same |
| DE69123228T2 (en) * | 1990-12-21 | 1997-03-13 | Matsushita Electric Ind Co Ltd | Process for producing a chemically adsorbed layer |
| CA2059733C (en) * | 1991-01-23 | 1999-10-05 | Kazufumi Ogawa | Water- and oil-repelling film and method of manufacturing the same |
-
1991
- 1991-11-18 JP JP3301819A patent/JP2637869B2/en not_active Expired - Lifetime
- 1991-12-06 EP EP91120973A patent/EP0491251B1/en not_active Expired - Lifetime
- 1991-12-06 DE DE69120226T patent/DE69120226T2/en not_active Expired - Lifetime
- 1991-12-09 CA CA002057250A patent/CA2057250C/en not_active Expired - Fee Related
- 1991-12-10 US US07/804,668 patent/US5225274A/en not_active Expired - Lifetime
- 1991-12-10 KR KR1019910022572A patent/KR960006088B1/en not_active IP Right Cessation
-
1993
- 1993-02-22 US US08/020,534 patent/US5324543A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0491251B1 (en) | 1996-06-12 |
| US5324543A (en) | 1994-06-28 |
| DE69120226D1 (en) | 1996-07-18 |
| KR960006088B1 (en) | 1996-05-08 |
| EP0491251A1 (en) | 1992-06-24 |
| US5225274A (en) | 1993-07-06 |
| KR920012353A (en) | 1992-07-25 |
| DE69120226T2 (en) | 1996-10-10 |
| JPH0596679A (en) | 1993-04-20 |
| CA2057250A1 (en) | 1992-06-11 |
| JP2637869B2 (en) | 1997-08-06 |
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