Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
  • C09K3/18—Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
  • C09K3/185—Thawing materials
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/28—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
  • C03C17/32—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with synthetic or natural resins
  • C03C17/322—Polyurethanes or polyisocyanates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/30—Low-molecular-weight compounds
  • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
  • C08G18/3893—Low-molecular-weight compounds having heteroatoms other than oxygen containing silicon
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
  • C08G18/4063—Mixtures of compounds of group C08G18/62 with other macromolecular compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/48—Polyethers
  • C08G18/4833—Polyethers containing oxyethylene units
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/61—Polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
  • C08G18/78—Nitrogen
  • C08G18/7806—Nitrogen containing -N-C=0 groups
  • C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
  • C08G18/7831—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing biuret groups
• • 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
  • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
  • C09D175/04—Polyurethanes
• • 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
  • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
  • H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
  • H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
  • H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
  • H01B3/302—Polyurethanes or polythiourethanes; Polyurea or polythiourea
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2290/00—Compositions for creating anti-fogging

Definitions

• the present invention relates to an anti-fogging coating that can be suitably used as an indoor window glass having a mechanism capable of controlling humidity, such as an air conditioner in an automobile interior.
• Transparent substrates such as glass are used for vehicle window glass, architectural window glass, lenses, goggles and the like.
• the glass is used in a highly humid place or at a boundary with a large temperature difference or humidity difference, condensation occurs on the surface and fogging occurs.
• dehumidified air such as warm air and cold air is applied to the window to ensure visibility. It is normal practice to blow and dry.
• Patent Document 1 discloses an antifogging automotive glass obtained by applying a composition containing an organic antifogging material to an ultraviolet low-transmitting glass.
• Patent Document 2 discloses a vehicle window glass in which a hydrophilic layer having a contact angle with water containing alumina on the interior surface of 30 ° or less is provided.
• Patent Document 1 discloses the use of a silica fine particle-based porous film and a water-absorbent coagulant as an anti-fogging property due to water absorption, but the water-absorbing ability of these water-absorbing films. However, further improvement was necessary for the development of anti-fogging properties due to sufficient water absorption. In addition, it was designed from the standpoint of developing anti-fogging properties in a sub-freezing environment, so it is expected that defects such as a decrease in translucency and film breakage due to freezing of the absorbed water may occur. It is done.
• an anti-fogging glass suitable for a vehicle window that makes it easy to ensure the visibility of the window even in a cold region where the environment may be below freezing (Patent Document 3).
• a coating made of urethane resin having hydrophilicity and water absorption is used in the antifogging glass.
• the antifogging property is designed such that the antifogging property is first manifested by water absorption of the coating, and the antifogging property is continued by the hydrophilicity of the coating after water absorption saturation. In addition, it has excellent scratch resistance due to its inherent elasticity.
• Patent Document 1 Japanese Patent Laid-Open No. 2000-239045
• Patent Document 2 JP 2003-321251 A
• Patent Document 3 Japanese Patent Laid-Open No. 2005-187276
• the present invention has a mechanism that exhibits anti-fogging properties only by water absorption of the film, has excellent durability, and forcibly dehydrates the film after water saturation of the film, such as the interior of an automobile. It is an object of the present invention to provide an antifogging film suitable for use in indoor environments.
• the antifogging film of the present invention is an antifogging film formed on a transparent substrate, and the film comprises a urethane resin having a water absorption of 20 to 40% by weight, and the urethane resin Is derived from an alkinorepository having an average molecular weight of 1000 to 4000 and a positive * 400 to 5000: xylanolylene polyol, and the coating is formed after water saturation of the coating. It is used in an indoor environment that has a mechanism for forced dehydration from the film. Do not form a water film when defogging is manifested! It is characterized by that.
• the mechanism for forcibly dehydrating the coating after water absorption saturation of the coating described above is a mechanism that can bring the surrounding environment of the coating from a cloudy environment to a non-fogging environment, such as a dehumidifying function, cold air or hot air.
• a non-fogging environment such as a dehumidifying function, cold air or hot air.
• An air conditioner or the like having a ventilation function such as a temperature adjustment function corresponds to the mechanism.
• the indoor environment is particularly assumed to be the interior of an automobile, and the use of the antifogging film is particularly preferably an automobile window glass.
• the fogging described above occurs when the temperature, humidity, and temperature of the coating film are at a certain condition. Therefore, the cloudy environment referred to in the present invention is a flow having a size of 100 mm x 100 mm x 3 mm (thickness). It is defined as the environment in which condensation occurs on the entire surface of a single sheet of soda-lime silicate glass.
• the anti-fogging film of the present invention does not form a water film when the anti-fogging property is exhibited, and the anti-fogging property is expressed only by the water absorption function of the film.
• the water absorption is saturated and the antifogging effect stops.
• it is better that the time is longer because water absorption is saturated.
• the time until water absorption is saturated correlates with the water absorption rate of the coating, but increasing the water absorption rate tends to decrease the strength and durability of the coating.
• the water absorption rate of the coating by setting the water absorption rate of the coating to 20 to 40% by weight, it is possible to achieve both a long time until water absorption is saturated and the durability of the coating. If it is less than 20% by weight, it is necessary to increase the film thickness in order to lengthen the time until water absorption is saturated, and it becomes difficult to obtain a uniform film. On the other hand, if it exceeds 40% by weight, problems such as increased stickiness of the coating, reduced strength, and poor water resistance arise.
• the coating used in the present invention is a coating that can be reversibly absorbed and desorbed. And excellent In order to obtain an anti-fogging coating, it is necessary to increase the rate of dewatering the water absorbed in the coating. If this speed is high, the amount of energy loaded on the defogger can be reduced. By using the antifogging film and the defogger together, it becomes possible to continuously exhibit the antifogging property. Further, since the water film is not formed when the anti-fogging property is exhibited, the fluoroscopic image does not fluctuate through the water film, so that it is suitable for use in an automobile window glass.
• the contact angle of water droplets on the film is more than 40 °, preferably in a state where water is not absorbed by the film, and in a saturated water absorption state. Is adjusted to be 50-: LO 0 °, preferably 60-90 °.
• the coating is made of urethane resin having a water absorption rate of 20 to 40% by weight
• the urethane resin is made of acrylic polyol having an average molecular weight of 1000 to 4000 and an average molecular weight of 400 to 5000.
• * * Increase the rate of dehydration of water absorbed in the coating by the chain in urethane resin derived from 1000-4000 axenoreposi-nore and: ⁇ h 3 ⁇ 4-400-5000 It is thought that he was successful.
• the polyoxyalkylene-based polyol mainly exerts a water-absorbing function on the film when it becomes a film.
• a polyol having an oxyethylene chain, an oxypropylene chain, or the like can be used as this polyol.
• the oxyethylene chain is excellent in the function of absorbing water as bound water, which is advantageous in achieving an antifogging film that exhibits reversible absorption and dehydration with a high dehydration rate during dehydration.
• the average molecular weight of the polyoxyalkylene-based polyol is 400 to 5000.
• the average molecular weight is less than 400, the ability to absorb water as bound water is low, and the average molecular weight exceeds 5000. In such a case, problems such as poor curing of the coating agent and a decrease in film strength are likely to occur.
• the average molecular weight is more preferably 400-4500.
• the average molecular weight in this invention is a number average molecular weight.
• the average molecular weight is preferably 400-2000.
• the average molecular weight is preferably 1500 to 5000.
• polyoxyalkylene-based polyol a plurality of types of polyols may be used.
• polyethylene glycol having an average molecular weight of 400 to 2000, which is particularly excellent in the ability to absorb water as bound water, must be used. It is preferable. Since the polyol is particularly excellent in the ability to absorb water as bound water, all polyoxyalkylene polyols may be used as the polyol.
• the acrylic polyol is intended to exert an effect of lowering the wear resistance, water resistance, and surface friction coefficient mainly on the film, that is, exhibiting slip property on the film surface.
• this acrylic polyol is effective in shortening the leveling step of making the film thickness uniform when the coating agent for forming the coating is applied to the substrate.
• the slip property is an important index from the practical viewpoint of the antifogging coating.
• Antifogging coatings are easily assumed to have a wide variety of deposits on the surface of the film during use, impairing the appearance and quality. Usually, in order to remove these deposits, cloth, etc. Wipe off at the site. At that time, if the slip property of the surface is insufficient, in the wiping operation, problems such as increased removal time and poor appearance due to uneven wiping occur.
• the adhering material is rubbed against the film surface. If the slip property is poor, the adhering material is often attracted to the film surface or immediately scratched, or used for the wiping operation. In some cases, the cloth or the like may adversely affect the film surface. High slipping on the membrane surface produces synergistic effects such as improved membrane wear resistance and antifouling properties.
• the antifogging coating of the present invention has a static friction coefficient of the coating obtained in accordance with "JIS K 7125". It is preferably 0.8 or less when not absorbing water and 0.9 or less when saturated with water. The lower limit of this coefficient may be 0.4 or more in consideration of the water absorption of the film.
• the acrylic polyol has an average molecular weight of 1000 to 4000.
• the polyol preferably has 3 or 4 hydroxyl groups.
• the dehydration rate of the water absorbed in the coating film is increased by the chain in the urethane resin formed by being derived from the polyoxyalkylene polyol and the acrylic polyol.
• the average molecular weight of the acrylic polyol is preferably 2000 or more.
• the acrylic polyol contributes to improving the durability of the coating and increasing the dehydration rate of water as described above. Considering only the improvement in the durability of the coating, it is possible to use a polyol having a hydrophobic property other than the acrylic polyol. This does not contribute to increasing the water dehydration rate. Therefore, it can be said that the acrylic polyol is an essential chemical species for obtaining the antifogging film of the present invention.
• the resin further includes 5 dimethylsiloxane units (Si (CH) O) as crosslinking units.
• linear polydimethylsiloxane that is 32-300.
• the linear polydimethylsiloxane is introduced into the resin by forming a urethane bond at the terminal portion.
• the number of (CH 3) O) is 5 to 300 because the number of dimethylsiloxane units is less than 5, or 3
• the linear polydimethylsiloxane is preferably added in an amount of 0.05 to 3.0% by weight with respect to the coating.
• the thicker the film is the more moisture is absorbed and the time until the film reaches the water absorption saturation state can be lengthened. It is advantageous to increase the film thickness of the coating.
• the thick film thickness brings disadvantageous conditions for the production of the film. Considering that it is cloudy for 60 seconds by exposure to 43 ° C saturated water vapor as an index, the film thickness is preferably 5 to 50 m.
• the anti-fogging film of the present invention is excellent in anti-fogging properties such as preventing fogging even in a sub-freezing environment, and therefore maintains optical properties such as translucency of the article in a cloudy environment. And even when the film is saturated with water absorption, it is used in combination with a mechanism that forcibly dehydrates the film, so that water can be dehydrated with high sensitivity and the film can be absorbed again, that is, an anti-fogging property is developed. Can be used. Therefore, when the anti-fogging article formed with the anti-fogging coating of the present invention is used as a window, it is easy to secure a field of view. When used as an automobile window, the effect is particularly remarkable. To improve safety and fuel efficiency.
• the antifogging film of the present invention is an antifogging film formed on a transparent substrate, and the film comprises a urethane resin having a water absorption of 20 to 40% by weight. These are derived from the polyol component of an axinorepository having an average molecular weight of 1000 to 4000 and a positive * 400 to 5000: xylanolene polyol.
• the antifogging article of the present invention is It consists of a cloudy film and a transparent substrate.
• the antifogging film can be obtained by applying and hardening a coating agent for forming an antifogging film on a transparent substrate.
• the coating agent can be a two-component curable coating agent comprising coating agent A having an isocyanate component having an isocyanate group and coating agent B having a polyol component.
• the isocyanate component is an organic polyisocyanate such as an organic diisocyanate, and preferably a trifunctional polyisocyanate having a pyrulet and Z or isocyanurate structure starting from hexamethylene diisocyanate. Nate can be used.
• the substance has weather resistance, chemical resistance and heat resistance, and is particularly effective for weather resistance.
• diisophorone diisocyanate, diphenylmethane diisocyanate, bis (methyl Oral hexyl) diisocyanate and toluene diisocyanate can also be used.
• the number of isocyanate groups present in the isocyanate component is 1 to 2 times, more preferably 1.4 times the number of hydroxyl groups present in the polyol component in the coating agent B. ⁇ 1. It is preferable to adjust so that the amount is 8 times. When the amount is less than 1 times, the curability of the coating agent is deteriorated, and the formed film has low durability such as soft weather resistance, solvent resistance, and chemical resistance. On the other hand, when the amount exceeds 2 times, the antifogging property is deteriorated because the water absorption and dehydration is inhibited by excessive curing.
• the ratio between the polyoxyalkylene-based polyol and the acrylic polyol is adjusted so that the film has a water absorption of 20 to 40% by weight.
• the ratio between the polyoxyalkylene-based polyol and the acrylic polyol is adjusted so that the film has a water absorption of 20 to 40% by weight.
• a diluent solvent can be added to the coating agents A and B or a mixture of the coating agents A and B.
• a diluting solvent it is necessary to use a solvent that is not active with respect to the isocyanate group. From the viewpoint of compatibility with these coating agents, it is preferable to use acetate solvents, ketones, and diacetone alcohol. .
• an organic tin compound as a curing catalyst may be added to the coating agents A and B or a mixture of the coating agents A and B in order to increase the curing rate of the coating film.
• These compounds include dibutyltin dilaurate, dioctyltin dilaurate, stannous octoate, dibutyltin ditatoate, dibutyltin diacetate, dibutyltin mercaptide, dibutyltin thiocarboxylate, dibutyltin dimaleate, dioctyltin mercaptide Dioctyltin thiocarboxylate and the like can be used.
• linear polydimethylsiloxane having functional groups capable of reacting with isocyanate groups at both ends is introduced into the coating agent B or a mixture of the coating agent A and the coating agent B.
• the linear polydimethylsiloxane that is preferably introduced can be introduced as a crosslinking unit in the resin forming the film.
• Examples of the functional group capable of reacting with the isocyanate group include oxygen having a large electronegativity such as a hydroxy group, a carboxy group, an amino group, an imino group, a mercapto group, a sulfino group, and a sulfo group, Functional groups containing active hydrogen bonded to nitrogen and sulfur can be used.
• oxygen having a large electronegativity such as a hydroxy group, a carboxy group, an amino group, an imino group, a mercapto group, a sulfino group, and a sulfo group
• Functional groups containing active hydrogen bonded to nitrogen and sulfur can be used.
• a hydroxy group as a functional group capable of reacting with an isocyanate group.
• a silicon compound may be introduced into the coating so that the water absorption rate is within the above-described range. Therefore, colloidal silica having an average particle diameter of 5 to 50 nm, a silicon compound having an alkoxy group, or the like may be introduced into the coating agent, particularly coating agent B.
• the average particle diameter is obtained by a method based on JIS H 7803 (2005).
• a coating agent for forming a film By mixing the coating agents A and B obtained as described above, a coating agent for forming a film can be obtained.
• known means such as spin coating, dip coating, flow coating, roll coating, spray coating, screen printing, flexographic printing and the like can be employed.
• the solution applied to the substrate is cured by standing at room temperature of about 20 ° C or heat treatment up to 170 ° C to form an antifogging film on the substrate. If the temperature of this heat treatment exceeds 170 ° C, care must be taken that carbonization of the urethane resin occurs and the film strength decreases. In consideration of acceleration of the coating, it is preferable to perform heat treatment at 80 ° C to 170 ° C.
• the glass is typically used as a transparent substrate for forming an antifogging film.
• the glass is a plate glass usually used for automobiles, architectural and industrial glasses, and is a plate glass by a float method, a duplex method, a roll-out method, etc., and the manufacturing method is not particularly limited.
• various colored glasses such as clear, green, bronze, etc.
• various functional glasses such as UV, IR cut glass, electromagnetic shielding glass, netted glass, low expansion glass, open expansion glass, etc. Glass that can be used for glass, tempered glass and similar glass, laminated glass, etc.
• the thickness is preferably 1. Omm or more and 5. Omm or less for a vehicle in which 1. Omm or more and 10mm or less are preferred.
• the antifogging film should be formed on the base material only on one side. However, depending on the application, it may be performed on both sides. In addition, the antifogging film may be formed on the entire surface or a part of the substrate surface.
• a liquid having a silane coupling agent is applied before application of the coating agent in order to improve the adhesion between the substrate and the coating. It is preferable to keep it.
• Suitable silane coupling agents include amino silanes, mercapto silanes and epoxy silanes. Preferred are ⁇ -glycidoxypropyltrimethoxysilane, y-aminopropyltriethoxysilane and the like.
• a resin film such as polyethylene terephthalate, a resin such as polycarbonate, and the like can be used.
• These resin transparent substrates can be used as antifogging articles and the articles can be affixed to a glass substrate, or a film comprising only an antifogging film component can be affixed to a substrate such as a glass substrate. ⁇ ⁇ .
• [0054] Water absorption rate of coating film]: Weight of anti-fogging article when held for 12 hours in an environment of 50% humidity and 55 ° C for 12 hours and then at an ambient temperature of 25 ° C for 12 hours ( a) was measured, and the coating was brought into contact with 43 ° C saturated water vapor for 5 minutes, and then immediately after wiping off the water film on the coating surface, the weight (b) of the article was measured, and [ba] / [a- ( Weight of glass substrate)] The value obtained by the calculation formula of X 100 (%) was defined as the water absorption at the time of water absorption saturation. That is, the water absorption is the percentage of water that can be absorbed relative to the weight of the anti-fogging coating, expressed as a percentage by weight. The value (a) here corresponds to that in a state where the film absorbs water.
• [0056] [Repeated anti-fogging property]: ⁇ Haze condition when kept for 1 minute in saturated steam of hot water set at 43 ° C according to JIS S 4030 Anti-fogging agent test method for glasses ⁇ , After holding the room temperature (2 Observe the cloudiness due to exhalation when taken out at 3 ° C and humidity 63%. This operation is one cycle for 30 cycles, and there is no abnormality in the appearance of the film and no clouding occurs! , The product passed (O), and the cloudy one was rejected (X). This evaluation can be used as an index of the sustainability of antifogging properties.
• [0057] Anti-fogging anti-fogging property: Appearance, cloudiness, and cloudiness due to exhalation when kept in a freezer set to -25 ° C for 30 minutes and then taken out at room temperature (23 ° C, humidity 63%) Observe. This operation was performed for 10 cycles. The film appearance was normal and the cloudiness did not occur was judged acceptable ( ⁇ ), and the cloudy appearance was rejected (X).
• [0059] [Pencil hardness]: In accordance with ⁇ JIS K 5600 paint general test method ⁇ , the film surface was drawn 5 times with a pencil with a load of 1 kg, and the film was broken less than 2 times. The pencil was defined as pencil hardness. The pencil hardness can be used as an index of scratch resistance.
• the coefficient of static friction derived from the measured values passes the test piece with water absorption of 0.8 or less in the state and 0.9 or less in the state of water absorption saturation ( ⁇ ) And those that did not satisfy this condition were judged as rejected (X).
• [0064] [Film thickness measurement]: A masking film (trade name “S PV-400X” manufactured by Nitto Denko) was affixed to a part of the base material during sample preparation to prepare an antifogging article. Then remove the masking film. Then, the film thickness of the film was measured by measuring the stepped portion formed by the film and the substrate with a high-precision fine shape measuring instrument (SUREFCORDER ET 4000A manufactured by Kosaka Laboratory).
• SUREFCORDER ET 4000A manufactured by Kosaka Laboratory
• Hexamethylene diisocyanate biuret type polyisocyanate (trade name “N3200” manufactured by Sumitomo Bayer Urethane) was used as coating agent A as an isocyanate having an isocyanate group.
• Polyethylene glycol having an average molecular weight of 1000, and an acrylic polyol and 50 weight 0/0 with a solution of average molecular weight 3000; Prepare ( "Desmophen A450MPAZX” by Sumika Baieruure Tan Inc.), the weight of polyethylene glycol and acrylic polyol The mixture was mixed so that the ratio was “polyethylene glycol: acrylic polyol 60: 40”.
• Coating agent of lOOg so that the number of isocyanate groups present in the isocyanate component of coating agent A is 1.6 times the number of hydroxyl groups present in the polyol component in coating agent B Add 33 g of coating agent A to B and mix and mix isobutyl acetate as a diluent solvent in the mixture of coating agent A and coating agent B so that the total amount of urethane components is 35% by weight.
• a coating agent for forming was prepared.
• y-Aminopropyltriethoxysilane (LS-3150, manufactured by Shin-Etsu Silicone Co., Ltd.) is modified with 90% ethanol by weight and 10% by weight isopropyl alcohol (Ekenen F-1, manufactured by Kishidai Chemical Co., Ltd.)
• the solution was prepared to 1 wt%.
• the solution is then Glass substrate surface of 100mm x 100mm (3.5mm thickness) obtained by float method with wiper made of absorbed cellulose fiber (trade name "Bencot", model M-1, 50mm x 50mm, manufactured by Ozu Sangyo)
• the solution was applied by wiping, and after drying at room temperature, the membrane surface was washed with water using a wiper to prepare a transparent substrate.
• the coating agent for forming the antifogging film obtained above is applied to the transparent substrate by spin coating, and the coated glass plate is heat-treated at about 100 ° C for about 30 minutes, An antifogging article having an antifogging film having a thickness of 16 ⁇ m was obtained.
• the amount of coating agent A added to 35g of lOOg was 35g so that the number was 1.8 times the number of hydroxyl groups present in the polyol component in coating agent B.
• the same operation as in Example 1 was performed to obtain an antifogging article on which an antifogging film having a film thickness of 27 / zm was formed. As shown in Table 1, the obtained article was confirmed to be an antifogging article excellent in various antifogging performances, various wear resistances, and water resistance.
• the same operation as in Example 1 was performed to obtain an antifogging article on which an antifogging film having a film thickness of 12 ⁇ m was formed. As shown in Table 1, the obtained article was confirmed to be an antifogging film excellent in various antifogging performances, various wear resistances, and water resistance.
• the obtained article was confirmed to be an antifogging film excellent in various antifogging performances, various abrasion resistances, and water resistance.
• Example 4 The same operation as in Example 4 was carried out except that a dimethylsiloxane unit having a number of dimethylsiloxane units of 243 and having both ends in a hydroxy linear polydimethylsiloxane (trade name “DMS-S27J”) was used. As shown in Table 1, the obtained antifogging article was formed with an antifogging film having various antifogging performance, various wear resistance, and water resistance. It was confirmed that there was. [0076] Comparative Example 1
• coating agent B do not use polyethylene glycol !, use only acrylic polyol, and determine the number of isocyanate groups present in the isocyanate component of coating agent A by the number of hydroxyl groups present in the polyol component in coating agent B.
• the same procedure as in Example 1 was conducted except that 18 g of coating agent A was added to lOOg coating agent B, and the film thickness was 11 m.
• An article on which a coating was formed was obtained. As shown in Table 1, the obtained article did not show any antifogging property.
• the number of isocyanate groups present in the isocyanate component of coating agent A is determined by the number of hydroxyl groups present in the polyol component in coating agent B.
• the same procedure as in Example 1 was carried out except that 5 lg of coating agent A was added to lOOg of coating agent B so that the amount was 1.4 times the amount.
• An antifogging article having a 28 m antifogging film was obtained. As shown in Table 1, the obtained article had a fabric that adhered to the film surface in the traverse abrasion resistance test, resulting in poor appearance and poor slip, and the film surface had a sticky feeling. It was. Further, in the [dehydration rate of water absorbed in the coating] test, it took 6 minutes for the water to be dehydrated, and the response of the water absorption / dehydration was poor.
• the amount of coating agent A added to lOOg coating agent B is 20 g so that the number of isocyanate groups to be applied is 1.4 times the number of hydroxyl groups present in the polyol component in coating agent B.
• the same operation as in Example 1 was performed to obtain an antifogging article on which an antifogging film having a film thickness of 15 m was formed.
• the obtained article was inferior in antifogging property as shown in Table 1. Comparative Example 5
• Example 1 In the preparation of coating agent B in Example 1, a poly force prolatatone diol having an average molecular weight of 500 (trade name “Platacel L205 8” manufactured by Daicel Engineering Co., Ltd.) was used as a polyol exhibiting hydrophobicity instead of acrylic polyol.
• an antifogging article having an antifogging film having a film thickness of 19 m was obtained.
• the resulting article had a fabric appearance in the traverse abrasion resistance test, resulting in poor appearance, and in the [Water resistance] test, the pencil hardness decreased by 2 ranks, resulting in water absorption. The scratch resistance of the coating at that time was inferior.
• the [dehydration rate of water absorbed by the film] test it took 5 minutes for the water to be dehydrated, and the response of the adsorption / desorption water was poor and it was also an article.

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