CN110300781A - Coating composition, film and the air conditioner with it - Google Patents
Coating composition, film and the air conditioner with it Download PDFInfo
- Publication number
- CN110300781A CN110300781A CN201780086583.6A CN201780086583A CN110300781A CN 110300781 A CN110300781 A CN 110300781A CN 201780086583 A CN201780086583 A CN 201780086583A CN 110300781 A CN110300781 A CN 110300781A
- Authority
- CN
- China
- Prior art keywords
- dispersion
- film
- coating composition
- fluororesin
- particle
- 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.)
- Granted
Links
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
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/12—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
-
- 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
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09D201/04—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing halogen atoms
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F1/00—Room units for air-conditioning, e.g. separate or self-contained units or units receiving primary air from a central station
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Paints Or Removers (AREA)
- Air-Conditioning Room Units, And Self-Contained Units In General (AREA)
- Air Filters, Heat-Exchange Apparatuses, And Housings Of Air-Conditioning Units (AREA)
- Duct Arrangements (AREA)
Abstract
The present invention is coating composition, it includes: the dispersion of the metal oxide particle comprising acrylic resin and selected from one or more of the group being made of tin oxide, antimony oxide and tungsten oxide；With the dispersion comprising fluororesin using fluorine series solvent as decentralized medium.Fluorine series solvent preferably has 5 or more and 50 kauri-butanol numbers (KB value) below.Relative to coating composition, the dispersion comprising fluororesin using fluorine series solvent as decentralized medium is preferably 1 mass % or more and 15 mass % or less.
Description
Technical field
The present invention relates to coating composition and its manufacturing method, film and forming method thereof and with the air-conditioning of the film
Machine.
Background technique
Indoors or the surface of various articles used in outdoor, due to various dirts such as dust, oil smoke and the tobacco tar of tobacco
Dirt attachment, therefore have studied the various methods that can inhibit it.For example, as it is known that: in the case where inhibiting the attachment of the dirts such as dust,
By being coated with antistatic agent on the surface of various articles, the attachment of the electrostatic of dust can inhibit.Additionally, it is known that: inhibiting oil smoke
In the case where attachment etc. lipophilic dirt, by being coated with the fluororesin of grease proofness on the surface of various articles, oleophylic can be made
Property dirt be easy remove.
But in the method for the attachment in the above-mentioned various dirts of inhibition, there is due to film removing, deterioration without
The problem of capable of maintaining long-term anti-pollution.Therefore, waterproofness envelope is recorded in patent document 1, which is characterized in that by extremely
The particle and antistatic resin compositions film that few surface is hydrophobic average grain diameter 1nm~1mm are constituted, and the particle is made to exist
Expose and adhere in 20% or more region of antistatic resin compositions film coated surface product.
It is that a surface side of substrate is provided with the hard coat film of hard conating in addition, recording hard coat film in patent document 2,
It is characterized in that, including in above-mentioned hard conating: having on the surface of the silicon dioxide microparticle of average 1 10~100nm of partial size
The reactive silica particle of reactive functional groups a be cross-linked with each other bonding made of structure, between above-mentioned silicon dioxide microparticle
Gap in fill: dissolve or be dispersed with conductibility antistatic agent or to be dispersed with average 1 partial size smaller than silicon dioxide microparticle
Functional particle Binder Composition, and the reactive functional groups a and Binder Composition on the surface of the silicon dioxide microparticle
The possessed partial cross-linked bonding of reactive functional groups b.
In addition, recording the substrate with hard coat film in patent document 3, which is characterized in that by substrate and on substrate
The hard coat film of formation is constituted, which includes matrix components and inorganic oxide particle group, and inorganic oxide particle group is
Made of inorganic oxide particle 2~30 in terms of average connective number are connected to chain, which is by dioxy
The silica-based particle that SiClx or silica alumina are constituted is in the internal hollow-particle with cavity, the matrix
Ingredient is made of heat reactive resin or ultraviolet curable resin.
Existing technical literature
Patent document
Patent document 1: Japanese Unexamined Patent Publication 8-134437 bulletin
Patent document 2: Japanese Unexamined Patent Publication 2010-241018 bulletin
Patent document 3: Japanese Patent No. 4540979
Summary of the invention
Subject to be solved by the invention
But in the technology of patent document 1, therefore existing cannot get since the water contact angle of antistatic property resin is small
The problem of sufficient waterproofness.In addition, in the technology of patent document 2, existing not only cannot get sufficient waterproofness but also resistance to
The low problem of abrasiveness.In addition, being had the following problems in the technology of patent document 3: in the internal hollow-particle with cavity
I.e. inorganic oxide particle 2~30 in terms of the average connective number catenulate inorganic oxide particle groups of connection make the saturating of hard coat film
Bright property reduces.
For the present invention, it completes to solve the problem above-mentioned, and it is an object of the present invention to provide coating composition, the coating
Composition is capable of providing the film for having the anti-pollution for various dirts, wear resistance, the transparency and high waterproofness.
Means for solving the problems
The present invention is coating composition, characterized by comprising: comprising acrylic resin and selected from by tin oxide, oxygen
Change the dispersion of the metal oxide particle of one or more of group of antimony and tungsten oxide composition；With using fluorine series solvent as dispersion
The dispersion comprising fluororesin of medium.
The effect of invention
In accordance with the invention it is possible to provide coating composition, the coating composition, which is capable of providing, to be had for a variety of dirts
Anti-pollution, wear resistance, the transparency and high waterproofness film.
Detailed description of the invention
Figure 1A is the schematic section for constituting the dispersion A for the coating composition that embodiment 1 is related to.
Figure 1B is the schematic section for constituting the dispersion B for the coating composition that embodiment 1 is related to.
Fig. 2 is the schematic section for the film that embodiment 1 is related to.
Fig. 3 is the dispersion A for constituting the coating composition that embodiment 1 is related to (comprising hydrophilic silicon oxides particle)
Schematic section.
Fig. 4 is the schematic section for the film (comprising hydrophilic silicon oxides particle) that embodiment 1 is related to.
Fig. 5 is the dispersion B for constituting the coating composition that embodiment 1 is related to (comprising hydrophobic silica particles)
Schematic section.
Fig. 6 is the schematic section for the film (comprising hydrophobic silica particles) that embodiment 1 is related to.
Fig. 7 is the summary sectional view for the air conditioner that embodiment 2 is related to.
Specific embodiment
Embodiment 1.
The coating composition that embodiments of the present invention 1 are related to includes: comprising acrylic resin and selected from by tin oxide,
Dispersion (the hereinafter sometimes referred to dispersion of the metal oxide particle of one or more of the group of antimony oxide and tungsten oxide composition
A)；With the dispersion (hereinafter sometimes referred to dispersion B) comprising fluororesin using fluorine series solvent as decentralized medium.Figure 1A is point
Dissipate the schematic section of object A.Figure 1B is the schematic section of dispersion B.
As shown in Figure 1A, dispersion A by the solvent 1 dissolved with acrylic resin and is being dissolved with acrylic resin
Solvent 1 in the metal oxide particle 2 that disperses constitute.Dispersion A preferably comprises 10 mass % or more and 80 mass % or less
Acrylic resin, more preferably include 20 mass % or more and 60 mass % or less.If the content of acrylic resin is not
To 10 mass %, becomes difficult to obtain sufficient film thickness when forming film, cannot fully play performance sometimes.On the other hand,
If the content of acrylic resin is more than 80 mass %, the excess stickiness of coating composition is increased sometimes.Acrylic resin
Mass ratio with metal oxide particle be preferably 60:40 or more and 98:2 hereinafter, more preferably 80:10 or more and 95:5 with
Under.If the mass ratio of acrylic resin and metal oxide particle is less than 60:40, film is excessively thinning, sometimes substrate
Expose.On the other hand, it if the mass ratio of acrylic resin and metal oxide particle is more than 98:2, is produced in film sometimes
Raw crackle.
As shown in fig. 1b, dispersion B is made of fluorine series solvent 4 and the fluororesin particle 3 being precipitated in fluorine series solvent 4.
Dispersion B preferably comprises 50 mass % or more and 99 mass % fluorine series solvents below, more preferably comprising 60 mass % or more and
90 mass % fluorine series solvents below.If less than 50 mass %, the solidifying of fluororesin particle occurs sometimes for the content of fluorine series solvent
It is poly-.On the other hand, if the content of fluorine series solvent is more than 99 mass %, defect is generated in film sometimes.In addition, dispersion B
1 mass % or more and 50 mass % fluororesin particle below are preferably comprised, more preferably includes 2 mass % or more and 45 mass %
Fluororesin particle below.If the content of fluororesin particle generates defect less than 1 mass % in film sometimes.Another party
If the content of fluororesin particle is more than 50 mass % the cohesion of fluororesin particle occurs sometimes for face.Fluororesin particle is averaged
Partial size is preferably 10nm or more and 1.0 μm hereinafter, more preferably 20nm or more and 900nm or less.If fluororesin particle is flat
Equal partial size is less than 10nm, and manufacture sometimes becomes difficult and the cohesiveness of fluororesin particle enhances and cannot form good film.
On the other hand, if the average grain diameter of fluororesin particle is more than 1.0 μm, volume ratio shared by fluororesin particle become larger and sometimes
Film gonorrhoea or electrification.It should be noted that the average grain diameter of so-called fluororesin particle, is measured by laser scattering method
Value.It, as shown in Figure 2, can if forming film by the coating composition for being obtained by mixing dispersion A and dispersion B
Film is formed on substrate 6, the film is by 5 shape of acrylic resin comprising metal oxide particle 2 and fluororesin particle 3
At, fluororesin particle 3 in surface distribution.The film of such form can be sent out in the state of maintaining anti-pollution and the transparency
Wave excellent waterproofness.
As acrylic resin, can enumerate UV curing type acrylic resin, a solution curing type acrylic resin,
Two-solution curing type acrylic resin etc..As UV curing type acrylic resin, preferably urethane acrylate and third
Olefin(e) acid system resin acrylate specifically can enumerate " ユ ニ デ ィ ッ Network (registered trademark) V- of Dainippon Ink Chemicals's manufacture
4005 ", " ユ ニ デ ィ ッ Network (registered trademark) V-4018 ", " ユ ニ デ ィ ッ Network (registered trademark) V-4025 ", " ユ ニ デ ィ ッ Network
(registered trademark) V-4026 ", " ユ ニ デ ィ ッ Network (registered trademark) V-4205 ", " ユ ニ デ ィ ッ Network (registered trademark) 15-829 ",
" ユ ニ デ ィ ッ Network (registered trademark) 17-813 ", " ユ ニ デ ィ ッ Network (registered trademark) 17-806 " and " ユ ニ デ ィ ッ Network (registrar
Mark) 17-824-9 ", Hitachi Chemical Co., Ltd. manufacture " ヒ タ ロ イ De (registered trademark) 7902-1 ", " ヒ タ ロ イ De
(registered trademark) 7909-1 ", " TA24-195H ", " ヒ タ ロ イ De (registered trademark) 7903-1 ", " ヒ タ ロ イ De (registrar
Mark) 7906D-3E ", " ヒ タ ロ イ De (registered trademark) 7975 ", " ヒ タ ロ イ De (registered trademark) 7988 " and " ヒ タ ロ イ
De (registered trademark) 7975D ", " 8BR-600 " and " 8BR-930MB " of the manufacture of great achievement Off ァ イ Application ケ ミ カ Le Co., Ltd. etc..
These UV curing type acrylic resins can be used alone, or two or more can be used.In these, from rapid-drying properties and dissolution
From the viewpoint of property, preferably " ユ ニ デ ィ ッ Network (registered trademark) 15-829 ", " ユ ニ デ ィ ッ Network (registered trademark) 17-813 ",
" ユ ニ デ ィ ッ Network (registered trademark) 17-806 " and " ユ ニ デ ィ ッ Network (registered trademark) 17-824-9 ".
As the concrete example of a solution curing type acrylic resin, " the ア Network リ デ ィ of Dainippon Ink Chemicals's manufacture can be enumerated
ッ Network (registered trademark) A-1300 ", " ア Network リ デ ィ ッ Network (registered trademark) A-1370 ", " ア Network リ デ ィ ッ Network (registered trademark) A-
1371 ", " ア Network リ デ ィ ッ Network (registered trademark) A-1380 ", " ア Network リ デ ィ ッ Network (registered trademark) A-181 " and " ア Network リ デ ィ ッ
" プ ラ ス ラ ッ Network #1200 ", " the プ ラ ス ラ ッ Network CV-1 " that Network (registered trademark) A-165 ", カ シ ュ ー Co., Ltd. manufacture
" プ ラ ス ラ ッ Network #1800 is serial (CP-1M CP-1X) " etc..These solution curing type acrylic resins can be used alone,
Or two or more can also be used.
As the concrete example of two-solution curing type acrylic resin, " the ア Network リ デ ィ of Dainippon Ink Chemicals's manufacture can be enumerated
ッ Network (registered trademark) A-837 ", " ア Network リ デ ィ ッ Network (registered trademark) A-814 ", " ア Network リ デ ィ ッ Network (registered trademark) A-
829 ", " ア Network リ デ ィ ッ Network (registered trademark) A-875-55 ", " ア Network リ デ ィ ッ Network (registered trademark) A-870 ", " ア Network リ デ ィ ッ
Network (registered trademark) A-871 " and " ア Network リ デ ィ ッ Network (registered trademark) 52-668-BA " etc..These two-solution curing type acrylic acid series
Resin can be used alone, or two or more can also be used.
As the solvent for dissolving acrylic resin, methanol, ethyl alcohol, propyl alcohol, 2- propyl alcohol, butanol, double third can be enumerated
Keto-alcohol, furfuryl alcohol, tetrahydrofurfuryl alcohol, ethylene glycol, hexylene glycol, diethyl ether, ethylene glycol single methyl ether, ethylene glycol monomethyl ether, ethylene glycol
Single-butyl ether, ethylene glycol isopropyl ether, diethylene glycol monomethyl ether, carbiphene, propylene glycol monomethyl ether, propylene glycol list
Ethylether, methyl acetate, ethyl acetate, isopropyl acetate, isobutyl acetate, butyl acetate, isoamyl acetate, amyl acetate,
Acetic acid 3- methoxybutyl, acetic acid 2- ethyl butyl ester, cyclohexyl acetate, ethylene glycol acetate, acetone, methyl ethyl ketone, methyl are different
Butyl ketone, butyl methyl ketone, cyclohexanone, methyl cyclohexanone, dipropyl ketone, methyl amyl ketone, diisobutyl ketone, toluene etc..This
A little solvents can be used alone, or two or more can also be used.In these, from the viewpoint of dissolubility and rapid-drying properties, preferably
Methyl acetate, ethyl acetate and isopropyl acetate.
For metal oxide particle, tin oxide (SnO can be enumerated2), antimony-doped tin oxide (ATO), phosphorus doping oxygen
Change tin (PTO), antimony oxide (Sb2O5), tungsten oxide etc..These metal oxide particles can be used alone, or can be used 2 kinds
More than.In these, from the viewpoint of the dispersion stabilization in coating composition, preferred antimony-doped tin oxide (ATO).
The average grain diameter of metal oxide particle be preferably 5nm or more and 60nm hereinafter, more preferably 10nm or more and
45nm or less.If the average grain diameter of metal oxide particle becomes difficult less than 5nm, manufacture, therefore not preferably.Another party
Face cracks in film, defect sometimes if the average grain diameter of metal oxide particle is more than 60nm.In turn, due to not having
Have using the catenulate inorganic oxide particle of connection such as patent document 3, therefore fouling material is not suspended on film, it is antifouling
Performance is improved.It should be noted that the average grain diameter of metal oxide particle is the value measured by laser scattering method.
In turn, as shown in Figure 3, dispersion A can further include scattered hydrophilic silicon oxides particle 8.Pass through
Dispersion A further includes hydrophilic silicon oxides particle 8, can be improved the antistatic property of film or further increases painting
The anti-pollution of film.If forming film by the coating composition for being obtained by mixing such dispersion A and dispersion B,
Then as shown in Figure 4, film can be formed on substrate 6, the film is by including metal oxide particle 2 and fluororesin particle 3
The formation of acrylic resin 5, fluororesin particle 3 with hydrophilic silicon oxides particle 8 is in surface distribution.With regard to hydrophily titanium dioxide
For the content of silicon particle, relative to dispersion A, preferably 0.5 mass % or more and 10 mass % hereinafter, more preferably 1 matter
Measure % or more and 8 mass % or less.If the content of hydrophilic silicon oxides particle cannot mention sometimes less than 0.5 mass %
The effect of high anti-pollution.On the other hand, if the content of hydrophilic silicon oxides particle is more than 10 mass %, film sometimes
Waterproofness reduces or film gonorrhoea and glossiness reduce.
As hydrophilic silicon oxides particle, it is able to use well known hydrophilic silicon oxides particle in the technical field.
As the concrete example of hydrophilic silicon oxides particle, " the organic silicon sol-of Nissan Chemical Ind Ltd's manufacture can be enumerated
MA-ST-M ", " organic silicon sol-MA-ST-L ", " organic silicon sol-IPA-ST-L ", " organic silicon sol-IPA-ST-ZL ",
" organic silicon sol-IPA-ST-UP ", " organic silicon sol-EG-ST ", " organic silicon sol-NPC-ST-30 ", " organic silicon sol-
PGM-ST ", " ス ノ ー テ ッ Network ス (registered trademark)-IPA-ST " and " ス ノ ー テ ッ Network ス (registered trademark)-DMAC-ST ",
" ア デ ラ イ ト (registered trademark) AT-30 ", " ア デ ラ イ ト (registered trademark) AT-40 " and " ア of Asahi Denka Co., Ltd.'s manufacture
" カ タ ロ イ De (registered trademark) SI- that デ ラ イ ト (registered trademark) AT-50 ", RiHui catalyst synthesis Co., Ltd manufacture
550 " and " カ タ ロ イ De (registered trademark) SI-50 " etc..
The average grain diameter of hydrophilic silicon oxides particle is preferably 5nm or more and 500nm hereinafter, more preferably 10nm or more
And 200nm or less.If the average grain diameter of hydrophilic silicon oxides particle becomes difficult less than 5nm, manufacture, therefore unexcellent
Choosing.On the other hand, if the average grain diameter of hydrophilic silicon oxides particle is more than 500nm, crack in film sometimes or
Person's film gonorrhoea.
As the fluororesin for constituting fluororesin particle, polytetrafluoroethylene (PTFE) (PTFE), hexafluoropropylene (HFP)/tetrafluoroethylene (TFE) can be enumerated
Copolymer (FEP), tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), ethylene-tetrafluoroethylene copolymer (ETFE), second
Alkene-chlorotrifluoroethylcopolymer copolymer (ECTFE), Kynoar (PVDF), polychlorotrifluoroethylene (PCTFE), polyvinyl fluoride
(PVF), vinyl fluoride-vinyl ether co-polymer, vinyl fluoride-vinyl ester copolymer, their mixture and in these fluororesin
In be mixed with the products etc. of other resins.In these, from dispersion in a solvent, with the jail for preventing decomposition caused by ultraviolet light
Solid bond energy, it is steady in a long-term from the viewpoint of, preferred vinyl fluoride-vinyl ether co-polymer.
Fluorine series solvent preferably has 5 or more and 50 kauri-butanol numbers (KB value) below.If the KB of fluorine series solvent
Value is less than 5, then fluororesin particle becomes difficult to be precipitated and waterproofness reduces sometimes.On the other hand, if the KB value of fluorine series solvent
More than 50, then manufacturing cost increases, therefore not preferably.As fluorine series solvent, CF can be enumerated3CF2CHCl2(HCFC-225ca)
Etc. hydrochlorofluorocarbons (HCFC), CHF2CF2OCH2CF3(HFE-347pc-f) hydrofluoroethers (HFE), the hydrofluorocarbon (HFC) etc. such as.These
In, from inhibit warmization from the viewpoint of, preferably ozone destruction coefficient (ODP) be zero compound.
Dissolve fluororesin with above-mentioned fluorine series solvent, but solids remains in order to prevent, it is possible to use to be dissolved in advance
Fluororesin 3 in solvent.Specifically, " Le ミ Off ロ Application (registered trademark) manufactured by Asahi Glass Co., Ltd can be enumerated
LF200 ", " Le ミ Off ロ Application (registered trademark) LF800 " and " Le ミ Off ロ Application (registered trademark) LF916 ", Dainippon Ink Chemicals's manufacture
" Off Le オ ネ ー ト (registered trademark) K-700 ", " Off Le オ ネ ー ト (registered trademark) K-702 ", " Off Le オ ネ ー ト (registration
Trade mark) K-704 ", " Off Le オ ネ ー ト (registered trademark) K-705 " and " Off Le オ ネ ー ト (registered trademark) K-707 " etc..
In turn, dispersion B can further include hydrophobic silica particles 7.As shown in Figure 5, hydrophobicity titanium dioxide
Silicon particle 7 is attached to the surface of fluororesin 3, or also sometimes a part of hydrophobic silica particles 7 are incorporated into fluororesin 3
In.For hydrophobic silica particles, concaveconvex structure is assigned to the surface of film, makes to reduce with the contact area of water droplet,
Thus, it is possible to improve waterproofness.If formed by the coating composition for being obtained by mixing such dispersion B and dispersion A
Film then as shown in Figure 6 can form film on substrate 6, the film by comprising metal oxide particle 2 and take in it is thin
The acrylic resin 5 of the fluororesin particle 3 of aqueous silicon dioxide granule 7 constitutes, takes in the fluorine of hydrophobic silica particles 7
Resin particle 3 is in surface distribution.For the content of hydrophobic silica particles, relative to dispersion B, preferably 5 matter
% or more and 50 mass % are measured hereinafter, more preferably 10 mass % or more and 30 mass % or less.If hydrophobic silica
The content of particle cannot improve the effect of waterproofness less than 5 mass % sometimes.On the other hand, if hydrophobic silica
The content of particle is more than 50 mass %, is cracked in film sometimes.
It as hydrophobic silica particles, is not particularly limited, is able to use well known hydrophobicity in the technical field
Silicon dioxide granule.Specifically, it as hydrophobic silica particles, is able to use and hydrophilic silicon oxides particle is dredged
The resulting product of hydration process.As hydrophilic silicon oxides particle, be not particularly limited, be able to use using dry method (such as
Combustion method), various silicon dioxide granules manufactured by wet process (such as sol-gal process, sedimentation) etc..In addition, titanium dioxide silicon grain
Son can be the silicon dioxide granule of part or all of melting.Wherein, it for dry silica, is generally possible to by making
The silicon compounds such as silicon tetrachloride burn in oxyhydrogen flame and are manufactured, also referred to as fumed silica.In dry method, pass through change
Manufacturing condition can obtain having about 50m2/ g~500m2The silicon dioxide granule of the specific surface area of the range of/g.Just by than table
It is the range of about 5nm~200nm, usually as 1 μm or more for the average grain diameter of area silicon dioxide granule calculated
Condensate exists.For wet silica, it is generally possible to make two in the solution and neutralizing sodium metasilicate inorganic acid
Silica is precipitated, and thus manufactures, also referred to as white carbon black.In addition, being also able to use substitution inorganic acid and neutralizing sodium metasilicate acid
Sol-gal process manufacture.In wet process, also it can obtain that there is about 50m by changing manufacturing condition2/ g~1000m2/g
Range specific surface area silicon dioxide granule.It, can be from above-mentioned various silica as hydrophilic silicon oxides particle
Selection has the silicon dioxide granule of average grain diameter appropriate depending on the application in particle.It is excellent from the viewpoint of accessibility
Choosing uses dry silica particle.
The silicic acid anhydride of hydrophilic silicon oxides particle is not particularly limited, it can be according to known in the technical field
Method carry out, it is preferable to use trimethylsilylation agent carry out silicic acid anhydride.By using trimethylsilylation
Agent can chronically maintain high waterproof performance.It as trimethylsilylation agent, is not particularly limited, is able to use the technology
Well known trimethylsilylation agent in field.As the example of trimethylsilylation agent, trimethyl silicane can be enumerated
Alkanol, trimethylmethoxysilane, trim,ethylchlorosilane, amino methyl trimethyl silane, hexamethyldisilazane, dimethylamino
Base trimethyl silane, diethylamino trimethyl silane etc.., it is preferable to use hexamethyldisilazane in these.These trimethyls
Silylating agent can be used alone, or two or more can be used.
The average grain diameter of hydrophobic silica particles is preferably 5nm or more and 30nm or less.It should be noted that with regard to hydrophobicity
For the average grain diameter of silicon dioxide granule, it is intended that when being measured using the particle size distribution meter of laser scattering type or dynamic light scattering formula
Hydrophobic silica particles primary particle average grain diameter value.If the average grain diameter of hydrophobic silica particles
Less than 5nm, it cannot be adequately formed fine concaveconvex structure on the surface of film, cannot get desired waterproof performance sometimes.
On the other hand, if the average grain diameter of hydrophobic silica particles is more than 30nm, the concaveconvex structure on surface excessively becomes larger, film
Durability reduce, and film light scattering become larger, sometimes substrate design reduce.
Dispersion A just comprising acrylic resin and metal oxide particle with using fluorine series solvent as decentralized medium
For the mixed proportion of dispersion B comprising fluororesin, relative to coating composition, dispersion B be preferably 1 mass % or more and
15 mass % are hereinafter, more preferably 2 mass % or more and 12 mass % or less.If the mixed proportion of dispersion B is less than 1 matter
% is measured, cannot get sufficient waterproofness sometimes.On the other hand, if the mixed proportion of dispersion B is more than 15 mass %, film
Electrification is become easy, therefore not preferably.In addition, for the mixing of dispersion A and dispersion B, it is more preferably following to carry out: so that
Fluorine series solvent contained in coating composition becomes 0.5 mass % or more and 14.0 mass % or less relative to coating composition.
If the content of fluorine series solvent is less than 0.5 mass %, fluororesin particle is not precipitated sometimes.On the other hand, if fluorine series solvent
Content be more than 14.0 mass %, sometimes coating composition viscosity reduce or evaporation rate it is too fast, formed after the drying
Defect is generated in film.
For the coating composition that embodiments of the present invention 1 are related to, it can be manufactured by the following method, the party
Method has: preparation is comprising acrylic resin and selected from one or more of the group being made of tin oxide, antimony oxide and tungsten oxide
Metal oxide particle dispersion A first step；Preparing using fluorine series solvent as decentralized medium includes fluororesin
The second step of dispersion B；With the dispersion of the dispersion of first step and the second step is carried out to be obtained by mixing coating group
Close the third step of object.For the preparation of the dispersion in first step and the second step, it can be used public in the technical field
The mixing machine known mixes above-mentioned each ingredient.In addition, can be used well known mixed in the technical field in the third step
Conjunction machine mixes dispersion A and dispersion B.
It for the film that embodiments of the present invention 1 are related to, can be formed by the following method, this method tool
It is standby: the process that above-mentioned coating composition is coated on substrate, is dried；With make the cured process of dry coating.
For the coating of coating composition, as long as the film of the surface coating composition of substrate can be covered
Method can enumerate dipping, spraying, hairbrush coating, rod coaters, curtain coating etc..In addition, coating composition is coated on substrate
Surface after, remaining coating composition can be removed with air-flow.Remaining coating composition substrate surface detention
In the case of, the film thickness for being formed by film in this section thickens, and cracks in film sometimes or film gonorrhoea.In turn,
Remaining coating composition dry flower is time-consuming, and do not obtain anti-pollution fully sometimes, therefore not preferably.For
For the method remaining coating composition removed with air-flow, dry facilitation effect caused by air-flow is also obtained, it may have
The advantages of good film easy to form.
Preferably 100 DEG C of the temperature of air-flow hereinafter, more preferable 60 DEG C or less.If the temperature of air-flow is excessively high, sometimes acrylic acid
It is that resin, fluororesin be rotten and the reduced performance of film.On the other hand, if the temperature of air-flow is 25 DEG C hereinafter, drying sometimes
Time is elongated without preferred.Temperature of the Time Dependent of jet-stream wind in air-flow, substrate shapes, therefore be not particularly limited, such as
Fruit is the substrate of simple shape, preferably 2 seconds or more and 20 seconds or less.If it is multiple with having as small gap, hole
The substrate of miscellaneous shape, the time of jet-stream wind preferably 5 seconds or more and 50 seconds or less.If the time of jet-stream wind is too short, have
When remaining coating composition residual.On the other hand, it if the overlong time of jet-stream wind, does not obtain fully sometimes antifouling
Performance.
It is preferably purple by being irradiated to dry coating in the case where acrylic resin is UV curing type acrylic resin
Outside line makes curing of coating.Exposure intensity is preferably 30W/cm2Above and 300W/cm2Hereinafter, irradiation time be preferably 3 minutes with
It is upper and 10 minutes or less.If exposure intensity is less than 30W/cm2, curing reaction is not sufficiently carried out sometimes.On the other hand, such as
Fruit exposure intensity is more than 300W/cm2, xanthochromia is cracked or occurred in film sometimes.In addition, if irradiation time less than
3 minutes, curing reaction was not sufficiently carried out sometimes.On the other hand, if irradiation time is more than 10 minutes, sometimes in film
It cracks, defect.
The case where acrylic resin is a solution curing type acrylic resin or two-solution curing type acrylic resin
Under, preferably make curing of coating by the way that dry coating is heated 30 minutes or more at 100 DEG C or less, preferably 60 DEG C or less.
The film thickness that film is formed by substrate is preferably 0.1 μm or more and 10 μm or less.If the film thickness of film is not
To 0.1 μm, anti-pollution is not obtained fully sometimes.On the other hand, if the film thickness of film is more than 10 μm, sometimes in film
In crack.
As substrate, it is able to use the portion for requiring the various products of anti-pollution, wear resistance, the transparency and high waterproofness
Part.As the example of such component, heat exchanger, fan, impeller, the wing flap (Off ラ ッ プ), wind path of air conditioner can be enumerated
Form component, cover etc..In addition, the material as substrate, such as polypropylene, polystyrene, ABS resin, ASG resin can be enumerated
Metals, the glass such as equal plastics, stainless steel, aluminium etc..
Embodiment 2.
Fig. 7 is the summary sectional view for the air conditioner that embodiments of the present invention 2 are related to.In Fig. 7, air conditioner 100 is main
Include shell 10, Air Blast fan 20 and heat exchanger 30.Shell 10 includes the suction inlet 11 of suction air and blows out air
Blow-off outlet 14.In addition, opening and closing is freely equipped with front grid 12 before shell 10.What is configured in shell 10 send
Wind fan 20 is constituted as follows: will be inhaled into from suction inlet 11 and by heat exchanger 30 by the air of heat exchange from blowout
Mouth 14 is sent out.Near suction inlet 11, configured with the filter 40 for capturing the dust contained in the air of suction.With regard to casing
The portion (ケ ー シ Application グ, portion) for 15, blow-off outlet 14 is extended to from the rear of Air Blast fan 20, determines the blowout of Air Blast fan 20
Direction.
For heat exchanger 30, be configured between suction inlet 11 and Air Blast fan 20, by make sucking air with
The refrigerant of refrigerating cycle carries out heat exchange to be reconciled (cooling, heating, dehumidifying, air-supply etc.).Heat exchanger 30 is to have
The fin tube heat exchanger of heat-transfer pipe 31 and the cooling fin 32 for inserting heat-transfer pipe 31.In addition, heat exchanger 30 is comprising preceding
The substantially inverted v-shaped (cross sectional shape of side view) of face overhead heat exchanger, front lower heat exchanger and back-surface heat exchanger.
In cannula portion 15, the fast wind of wind speed is collided, is adhered to via the dew that heat exchanger 30 flies here sometimes.Separately
Outside, near the suction side close to the cannula portion 15 of Air Blast fan 20, if from the heat-insulated insufficient of the back side of shell 10 or
Warm air immerses, then dew usually adheres to arranges at laterally one.
Near blow-off outlet 14, it is provided with the air that will be blown out from blow-off outlet 14 curved left and right in the lateral direction
Impeller 13 and in the up-down direction curved wing flap 17 up and down.Left and right impeller 13 is the various outline shapes being formed by resin
Multiple are arranged in the width direction (left and right directions) of machine (being known as air conditioner 100 in Fig. 7) indoors in flat wind direction board.In addition,
Upper and lower wing flap 17 is that the section being formed by resin is the wind direction board of substantially arc-shaped, indoors the entire width of the blow-off outlet 14 of machine
It is arranged on direction (left and right directions).For left and right impeller 13 and up and down wing flap 17, it can automatically change angle by motor.On
Lower wing flap 17 can be divided into wing flap, lower wing flap, can have multi-disc.
It is explained, in Fig. 7, heat exchanger 30 is matched in a manner of the top surface side for surrounding Air Blast fan 20 and front side
It sets, but present embodiment is not limited to the configuration.In addition, heat exchanger 30 is had heat-transfer pipe 31 and inserts heat-transfer pipe 31
Cooling fin 32 show as an example, but it's not limited to that for present embodiment.In addition, the air conditioner 100 of Fig. 7 is wall hanging
Type, but it's not limited to that for present embodiment.
The air conditioner that embodiments of the present invention 2 are related to grid 12, left and right impeller 13, cannula portion 15, the upper and lower flap in front
The surface of any one of the wing 17, Air Blast fan 20 and heat exchanger 30 is formed with the film that embodiment 1 is related to.With regard to embodiment party
For the film that formula 1 is related to, due to showing excellent anti-pollution, it is most suitable for making in the various components of air conditioner
With.Therefore, the air conditioner that embodiments of the present invention 2 are related to can be effectively prevented reduced performance and dirt of air conditioner etc. pair
In the attachment of air conditioner.
It should be noted that being formed with what embodiment 1 was related to for the surface of the component in air conditioner in embodiment 2
The example of film is illustrated, but also can be in each component of the electrical equipments such as ventilation fan, elevator, refrigerator, solar battery
Form the film that embodiment 1 is related to.
Embodiment
The present invention is specifically described in embodiment described below, but the present invention is by any restrictions of these embodiments,
Various applications can be carried out in the range of not departing from technical scope of the invention.
In following Examples and Comparative Examples, as substrate, 100mm × 30mm × 1mm plastic basis material (ABS is used
Resin base material).
[embodiment 1]
Make fluororesin " Dainippon Ink Chemicals Off Le オ ネ ー ト (registered trademark) K-702 " (fluororesin concentration: 50 matter
Amount %, solvent: toluene) it is dissolved in fluorine series solvent " Asahi Glass Co., Ltd ア サ ヒ Network リ Application (registered trademark) AE-3000 "
(CHF2CF2OCH2CF3, KB value: 12), prepare dispersion B.The fluororesin particle of average grain diameter 520nm is precipitated in dispersion B.
Then, in acrylic resin " Dainippon Ink Chemicals ユ ニ デ ィ ッ Network (registered trademark) 17-824-9 " (carbamate propylene
The concentration of acid esters: 79.8 mass %, solvent: isopropanol) in mixed-metal oxides particle " RiHui catalyst synthesis Co., Ltd's system
ELCOM (registered trademark)-V350 " (antimony-doped tin oxide particle concentration: 15 mass %, average grain diameter: 40nm) and isopropanol are mixed
It closes, prepares dispersion A.
Then, dispersion A and dispersion B is mixed, manufactures the coating composition of the embodiment 1 of composition shown in table 1.
The coating composition is coated on substrate, is made it dry.In turn, after 1 minute being made it dry at 70 DEG C, high-pressure sodium lamp pair is used
Dry coating irradiates ultraviolet light (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 5.2 μ
m。
[embodiment 2]
Similarly to Example 1, the coating composition of the embodiment 2 of composition shown in table 1 is manufactured.By the coating compositions
Object is coated on substrate, makes it dry.In turn, after 1 minute being made it dry at 70 DEG C, dry coating is irradiated using high-pressure sodium lamp
Ultraviolet light (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 5.5 μm.
[embodiment 3]
Similarly to Example 1, the coating composition of the embodiment 3 of composition shown in table 1 is manufactured.By the coating compositions
Object is coated on substrate, makes it dry.In turn, after 1 minute being made it dry at 70 DEG C, dry coating is irradiated using high-pressure sodium lamp
Ultraviolet light (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 5.0 μm.
[embodiment 4]
Make fluororesin " Dainippon Ink Chemicals Off Le オ ネ ー ト (registered trademark) K-702 " (fluororesin concentration: 50 matter
Amount %, solvent: toluene) it is dissolved in fluorine series solvent " Asahi Glass Co., Ltd ア サ ヒ Network リ Application (registered trademark) AE-3000 "
(CHF2CF2OCH2CF3, KB value: 12) after, mix hydrophobic silica particles " Japanese ア エ ロ ジ Le Co. Ltd. system ア エ
ロ ジ Le RX300 " (specific surface area: 210 ± 20m2/ g), prepare dispersion B.The fluorine of average grain diameter 532nm in dispersion B
Resin particle is precipitated.Then, at acrylic resin " Dainippon Ink Chemicals ユ ニ デ ィ ッ Network (registered trademark) 17-824-9 "
Mixed-metal oxides particle " waves touching day in (concentration of urethane acrylate: 79.8 mass %, solvent: isopropanol)
Matchmaker is melted into Co. Ltd. system ELCOM (registered trademark)-V350 " (antimony-doped tin oxide particle concentration: 15 mass %, average grain diameter:
40nm) and isopropanol, dispersion A is prepared.
Then, dispersion A and dispersion B is mixed, manufactures the coating composition of the embodiment 4 of composition shown in table 1.
The coating composition is coated on substrate, is made it dry.In turn, after 1 minute dry at 70 DEG C, using high-pressure sodium lamp to drying
Film irradiates ultraviolet light (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 5.9 μm.
[embodiment 5]
The coating composition of the embodiment 5 of composition shown in table 1 is manufactured similarly to Example 1.By the coating compositions
Object is coated on substrate, makes it dry.In turn, after 1 minute dry at 70 DEG C, dry coating is irradiated using high-pressure sodium lamp ultraviolet
Line (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 2.9 μm.
[embodiment 6]
The coating composition of the embodiment 6 of composition shown in table 1 is manufactured similarly to Example 1.By the coating compositions
Object is coated on substrate, makes it dry.In turn, after 1 minute dry at 70 DEG C, dry coating is irradiated using high-pressure sodium lamp ultraviolet
Line (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 5.0 μm.
[embodiment 7]
Make fluororesin " Dainippon Ink Chemicals Off Le オ ネ ー ト (registered trademark) K-702 " (fluororesin concentration: 50 matter
Amount %, solvent: toluene) it is dissolved in fluorine series solvent " Asahi Glass Co., Ltd ア サ ヒ Network リ Application (registered trademark) AE-3000 "
(CHF2CF2OCH2CF3, KB value: 12), prepare dispersion B.The fluororesin particle of average grain diameter 568nm is precipitated in dispersion B.
Then, in acrylic resin " Dainippon Ink Chemicals ユ ニ デ ィ ッ Network (registered trademark) 17-824-9 " (carbamate propylene
The concentration of acid esters: 79.8 mass %, solvent: isopropanol) in by metal oxide particle " RiHui catalyst synthesis Co., Ltd's system
ELCOM (registered trademark)-V350 " (antimony-doped tin oxide particle concentration: 15 mass %, average grain diameter: 40nm), hydrophily dioxy
SiClx particle " Nissan Chemical Ind Ltd organic silicon sol IPA-ST-ZL " (silicon dioxide granule concentration: 30 matter
Measure %, average grain diameter: 100nm) and isopropanol mixing, prepare dispersion A.
Then, dispersion A and dispersion B is mixed, manufactures the coating composition of the embodiment 7 of composition shown in table 1.
The coating composition is coated on substrate, is made it dry.In turn, after 1 minute being made it dry at 70 DEG C, high-pressure sodium lamp pair is used
Dry coating irradiates ultraviolet light (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 5.0 μ
m。
[comparative example 1]
In acrylic resin " Dainippon Ink Chemicals ユ ニ デ ィ ッ Network (registered trademark) 17-824-9 " (carbamate
The concentration of acrylate: 79.8 mass %, solvent: isopropanol) in mixed-metal oxides particle " wave day catalyst chemical conversion the meeting of strain formula
Society ELCOM (registered trademark)-V350 " (antimony-doped tin oxide particle concentration: 15 mass %, average grain diameter: 40nm) and isopropyl
Alcohol prepares the dispersion A of composition shown in table 1.Dispersion A is coated on substrate, is made it dry.In turn, at 70 DEG C
After making it dry 1 minute, ultraviolet light (80W/cm is irradiated to dry coating using high-pressure sodium lamp2) 1 minute, make its solidification, makes
Substrate with film.The film thickness of film is 4.2 μm.
[comparative example 2]
In addition to there is no complexed metal oxide particle " RiHui catalyst synthesis Co., Ltd ELCOM (registered trademark)-
Other than V350 ", the coating composition of the comparative example 2 of composition shown in table 1 is manufactured similarly to Example 1.By the coating group
It closes object and is coated on substrate, make it dry.In turn, after 1 minute being made it dry at 70 DEG C, dry coating is shone using high-pressure sodium lamp
Penetrate ultraviolet light (80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 5.2 μm.
[comparative example 3]
In addition to do not have cooperation acrylic resin " Dainippon Ink Chemicals ユ ニ デ ィ ッ Network (registered trademark) 17-824-9 " with
Outside, the coating composition of the comparative example 3 of composition shown in table 1 is manufactured similarly to Example 1.The coating composition is coated with
In substrate, make it dry.In turn, after 1 minute being made it dry at 70 DEG C, ultraviolet light is irradiated to dry coating using high-pressure sodium lamp
(80W/cm2) 1 minute, make its solidification, production has the substrate of film.The film thickness of film is 2.2 μm.
[table 1]
In accordance with the following methods to the anti-pollution of the obtained substrate with film, water contact angle, full light transmittance, mist
Degree and wear resistance are evaluated.It shows the result in table 2.
For anti-pollution, by (being closed to the sand dust as hydrophily fouling material with 1~3 μm of JIS for center partial size
Eastern soil dust) and the carbon black as hydrophobic contaminant matter mixture (analog composite dirt) adherence evaluated come
It carries out.Under the conditions of 25 DEG C/humidity of temperature 50%, after the mixture of sand dust and carbon black is ejected into film with air, pass through glue
Tape (manufacture of Sumitomo 3M company) is connect to sample, is surveyed by spectrophotometer (Shimadzu Corporation UV-3100PC)
Determine absorbance (wavelength 550nm), is evaluated according to following standards.Absorbance is smaller, it may be said that anti-pollution is the better.
< absorbance >
1: less than 0.1
2:0.1 or more and less than 0.2
3:0.2 or more and less than 0.3
4:0.3 or more and less than 0.4
More than 5:0.4
Contact angle meter (republicanism interface is used for placing 1 hour film under room temperature (25 DEG C) for water contact angle
Scientific Co. Ltd. system CX-150 type), it will about 5 μ L from the top of the needle for being coated with PTFE (polytetrafluoroethylene (PTFE)) of internal diameter 0.1mm
Water droplet drip to the surface of film, measure its contact angle, evaluated according to following standards.Water contact angle is bigger, it may be said that anti-
It is aqueous the better.
< water contact angle >
1:120 degree or more and less than 150 degree
2:100 degree or more and less than 120 degree
3:80 degree or more and less than 100 degree
4:60 degree or more and less than 80 degree
5: less than 60 degree
For full light transmittance and mist degree, measured by haze meter (Nippon Denshoku Industries Co., Ltd. NDH2000)
Haze value and transmissivity are evaluated according to following standards.Haze value is smaller and transmissivity is bigger, it may be said that the transparency is better
It is good.
< haze value >
1:0 or more and less than 1.0
2:1.0 or more and less than 3.0
3:3.0 or more and less than 5.0
4:5.0 or more and less than 7.0
More than 5:7.0
< transmissivity >
1:95% or more and less than 100%
2:90% or more and less than 95%
3:80% or more and less than 90%
4:60% or more and less than 80%
5: less than 60%
For wear resistance, by using Crock meter (colour fastness to rubbing testing machine), (Tian Jingji pacifies in Co., Ltd.
Manufactured by production) with load 1000gf/cm2 behind reciprocal 500 times of the surface of film, the exfoliated state of evaluation film carries out.
For the exfoliated state of the film after wear test, using electron microscope, image procossing is carried out to the exfoliated state of film,
Stripping area ratio is calculated, is evaluated according to following standards.
< wear resistance >
1: the stripping area ratio of film is less than 1%
2: the stripping area ratio of film is 1% or more and less than 20%
3: the stripping area ratio of film is 20% or more and less than 60%
4: the stripping area ratio of film is 60% or more and less than 90%
5: the stripping area ratio of film is 90% or more
[table 2]
| Absorbance | Water contact angle | Haze value | Transmissivity | Wear resistance | |
| Embodiment 1 | 1 | 2 | 2 | 2 | 1 |
| Embodiment 2 | 2 | 2 | 1 | 3 | 1 |
| Embodiment 3 | 3 | 1 | 2 | 2 | 3 |
| Embodiment 4 | 1 | 1 | 1 | 1 | 1 |
| Embodiment 5 | 4 | 2 | 3 | 3 | 2 |
| Embodiment 6 | 4 | 2 | 1 | 1 | 1 |
| Embodiment 7 | 1 | 3 | 1 | 2 | 1 |
| Comparative example 1 | 3 | 5 | 1 | 1 | 1 |
| Comparative example 2 | 5 | 2 | 1 | 1 | 2 |
| Comparative example 3 | 4 | 3 | 4 | 4 | 5 |
As shown in table 2, for the film formed by the coating composition of Examples 1 to 7, anti-pollution, the transparency,
Waterproofness and excelling in abrasion resistance.Wherein, anti-pollution, transparent for the film formed by the coating composition of embodiment 4
Property, waterproofness and wear resistance are the best.
In contrast, for the film formed by the coating composition of comparative example 1, the result that waterproofness is deteriorated is formed.
In addition, forming the result that anti-pollution is deteriorated for the film formed by the coating composition of comparative example 2.Just by comparative example 3
Coating composition formed film for, all formed at all aspects of anti-pollution, the transparency, waterproofness and wear resistance
The result of difference.
As can be known from the above results, have anti-pollution, wear resistance, the transparency and height in accordance with the invention it is possible to provide
The film of waterproofness.
The explanation of appended drawing reference
1 is dissolved with solvent, 2 metal oxide particles, the 3 fluororesin particles, 4 fluorine series solvents, 5 of acrylic resin
Acrylic resin, 6 substrates, 7 hydrophobic silica particles, 8 hydrophilic silicon oxides particles, 10 shells, 11 suckings
Mouth, 12 front grids, 13 or so impellers, 14 blow-off outlets, 15 cannula portions, about 17 wing flaps, 20 Air Blast fans, 30 heat are handed over
Parallel operation, 31 heat-transfer pipes, 32 cooling fins, 40 filters, 100 air conditioners.
Claims (11)
1. a kind of coating composition, characterized by comprising:
Metal comprising acrylic resin and selected from one or more of the group being made of tin oxide, antimony oxide and tungsten oxide
The dispersion of oxide particle；With
The dispersion comprising fluororesin using fluorine series solvent as decentralized medium.
2. coating composition according to claim 1, which is characterized in that the fluorine series solvent has 5 or more and 50 or less
Kauri-butanol number (KB value).
3. coating composition according to claim 1 or 2, which is characterized in that the acrylic resin and the metal
The mass ratio of oxide particle is 60:40 or more and 98:2 or less.
4. coating composition described in any one of claim 1 to 3, which is characterized in that relative to the coating compositions
Object, the dispersion comprising fluororesin using fluorine series solvent as decentralized medium are 1 mass % or more and 15 mass % or less.
5. coating composition according to any one of claims 1 to 4, which is characterized in that the average grain of the fluororesin
Diameter is 10nm or more and 1.0 μm or less.
6. coating composition according to any one of claims 1 to 5, which is characterized in that it is described using fluorine series solvent as
The dispersion comprising fluororesin of decentralized medium also includes hydrophobic silica particles.
7. coating composition described according to claim 1~any one of 6, which is characterized in that described includes acrylic acid series tree
The dispersion of rouge and metal oxide particle also includes average grain diameter 5nm or more and 500nm hydrophilic silicon oxides grain below
Son.
8. a kind of manufacturing method of coating composition, which is characterized in that have:
Preparation includes acrylic resin and the gold selected from one or more of the group being made of tin oxide, antimony oxide and tungsten oxide
Belong to the first step of the dispersion of oxide particle；
Prepare the second step of the dispersion comprising fluororesin using fluorine series solvent as decentralized medium；With
The dispersion of the dispersion of the first step and the second step is obtained by mixing to the third work of coating composition
Sequence.
9. a kind of forming method of film, which is characterized in that have:
The process that coating composition according to any one of claims 1 to 7 is coated on substrate, is dried；With
Make the cured process of dry coating.
10. a kind of film, by including the metal selected from one or more of the group being made of tin oxide, antimony oxide and tungsten oxide
The acrylic resin of oxide particle and fluororesin is formed, and has 0.1 μm or more and 10 μm of film thickness below, feature exist
In,
The fluororesin as particle in surface distribution, and its average grain diameter be 10nm or more and 1.0 μm or less.
11. a kind of air conditioner, which has: that takes in gas takes in mouth；It will be from the heat for takeing in the gas that mouth is taken in
The heat exchanger swapped；Make the fan recycled by the heat exchanger by the gas of heat exchange；It is formed by described
The wind path forming component in the channel of fan and transported gas；The gas that guidance is attracted by the wind path forming component
Impeller and wing flap；With the cover of the built-in heat exchanger and the fan, which is characterized in that
In any of the heat exchanger, the fan, the impeller, the wing flap, the wind path forming component and the cover
A surface has film according to claim 10.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/JP2017/006386 WO2018154630A1 (en) | 2017-02-21 | 2017-02-21 | Coating composition, coating film and air conditioner including same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN110300781A true CN110300781A (en) | 2019-10-01 |
| CN110300781B CN110300781B (en) | 2021-08-27 |
Family
ID=63254407
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201780086583.6A Active CN110300781B (en) | 2017-02-21 | 2017-02-21 | Coating composition, coating film, and air conditioner having same |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JP6625262B2 (en) |
| CN (1) | CN110300781B (en) |
| WO (1) | WO2018154630A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20190338150A1 (en) * | 2018-05-02 | 2019-11-07 | Ppg Industries Ohio, Inc. | Surface Active Coating Composition |
| JP6698955B1 (en) * | 2019-03-25 | 2020-05-27 | 三菱電機株式会社 | Coating film and method for forming the same, coating composition and method for producing the same, and centrifugal blower and air conditioner having the coating film |
Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002167571A (en) * | 2000-12-01 | 2002-06-11 | Nippon Yushi Basf Coatings Kk | Stainproof treatment agent, method for stainproof treatment and stainproof-treated article |
| WO2002087339A1 (en) * | 2001-04-30 | 2002-11-07 | Ak Properties, Inc. | Antimicrobial powder coated metal sheet |
| JP2003165955A (en) * | 2001-09-21 | 2003-06-10 | Kanegafuchi Chem Ind Co Ltd | Top coat curable resin coating material composition and its coated product |
| WO2004007594A1 (en) * | 2002-07-12 | 2004-01-22 | The University Of Western Ontario | Fluidization additives to fine powders |
| JP2005344052A (en) * | 2004-06-04 | 2005-12-15 | Daikin Ind Ltd | Solvent type coating composition |
| JP2011207924A (en) * | 2010-03-29 | 2011-10-20 | Lixil Corp | Antifouling coating and product coated therewith |
| WO2012017553A1 (en) * | 2010-08-06 | 2012-02-09 | リケンテクノス株式会社 | Coating composition and laminate |
| CN102356134A (en) * | 2009-03-19 | 2012-02-15 | 三菱电机株式会社 | Coating composition, coating process, air conditioner, ventilating fan, and electrical equipment |
| JP2012046674A (en) * | 2010-08-27 | 2012-03-08 | Asahi Glass Co Ltd | Coating composition and method manufacturing the same |
| CN103328590A (en) * | 2011-04-22 | 2013-09-25 | 松下电器产业株式会社 | Antifouling film, air blower blade provided with same, air blower, and antifouling coating material |
| CN103781871A (en) * | 2012-03-22 | 2014-05-07 | 日本特殊塗料株式会社 | Frost preventive coating composition |
| CN103897470A (en) * | 2012-12-27 | 2014-07-02 | 日挥触媒化成株式会社 | Base material provided with hard coating film and coating liquid formed by the hard coating film |
| CN105264010A (en) * | 2013-06-13 | 2016-01-20 | 大金工业株式会社 | Fluorine resin composition, coating film, and article |
| CN105722925A (en) * | 2013-11-29 | 2016-06-29 | 松下知识产权经营株式会社 | Coating material composition, and light-diffusing member manufactured using said coating material composition |
-
2017
- 2017-02-21 CN CN201780086583.6A patent/CN110300781B/en active Active
- 2017-02-21 WO PCT/JP2017/006386 patent/WO2018154630A1/en active Application Filing
- 2017-02-21 JP JP2019501786A patent/JP6625262B2/en active Active
Patent Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002167571A (en) * | 2000-12-01 | 2002-06-11 | Nippon Yushi Basf Coatings Kk | Stainproof treatment agent, method for stainproof treatment and stainproof-treated article |
| WO2002087339A1 (en) * | 2001-04-30 | 2002-11-07 | Ak Properties, Inc. | Antimicrobial powder coated metal sheet |
| JP2003165955A (en) * | 2001-09-21 | 2003-06-10 | Kanegafuchi Chem Ind Co Ltd | Top coat curable resin coating material composition and its coated product |
| WO2004007594A1 (en) * | 2002-07-12 | 2004-01-22 | The University Of Western Ontario | Fluidization additives to fine powders |
| JP2005344052A (en) * | 2004-06-04 | 2005-12-15 | Daikin Ind Ltd | Solvent type coating composition |
| CN102356134A (en) * | 2009-03-19 | 2012-02-15 | 三菱电机株式会社 | Coating composition, coating process, air conditioner, ventilating fan, and electrical equipment |
| JP2011207924A (en) * | 2010-03-29 | 2011-10-20 | Lixil Corp | Antifouling coating and product coated therewith |
| WO2012017553A1 (en) * | 2010-08-06 | 2012-02-09 | リケンテクノス株式会社 | Coating composition and laminate |
| JP2012046674A (en) * | 2010-08-27 | 2012-03-08 | Asahi Glass Co Ltd | Coating composition and method manufacturing the same |
| CN103328590A (en) * | 2011-04-22 | 2013-09-25 | 松下电器产业株式会社 | Antifouling film, air blower blade provided with same, air blower, and antifouling coating material |
| CN103781871A (en) * | 2012-03-22 | 2014-05-07 | 日本特殊塗料株式会社 | Frost preventive coating composition |
| CN103897470A (en) * | 2012-12-27 | 2014-07-02 | 日挥触媒化成株式会社 | Base material provided with hard coating film and coating liquid formed by the hard coating film |
| CN105264010A (en) * | 2013-06-13 | 2016-01-20 | 大金工业株式会社 | Fluorine resin composition, coating film, and article |
| CN105722925A (en) * | 2013-11-29 | 2016-06-29 | 松下知识产权经营株式会社 | Coating material composition, and light-diffusing member manufactured using said coating material composition |
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2018154630A1 (en) | 2019-07-04 |
| WO2018154630A1 (en) | 2018-08-30 |
| JP6625262B2 (en) | 2019-12-25 |
| CN110300781B (en) | 2021-08-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4698721B2 (en) | Air conditioner and coating composition | |
| US8801850B2 (en) | Coating composition, and its production, heat exchanger and air conditioner | |
| CN107614637B (en) | Coating composition, method for producing coating composition, coating film, ventilation fan, and air conditioner | |
| JP5202467B2 (en) | Blower | |
| JP5436480B2 (en) | Water-repellent film-forming coating composition, method for producing the same, and water-repellent member | |
| JP2009229040A (en) | Heat exchanger and manufacturing method of heat exchanger | |
| JP6381483B2 (en) | Coating composition, antifouling member, air conditioner and ventilation fan | |
| JP5121306B2 (en) | Blower fan and method of coating fan | |
| JP2011208937A (en) | Air conditioner and coating composition | |
| CN110300781A (en) | Coating composition, film and the air conditioner with it | |
| JP5581266B2 (en) | Paint and air conditioner | |
| JP2017061626A (en) | Coating composition, coating film, electronic equipment, air conditioner, coating method, and method for manufacturing air conditioner | |
| JP5888711B2 (en) | COATING COMPOSITION AND MANUFACTURING METHOD THEREOF, AND WATER-REPELLENT MEMBER AND VENTILATOR | |
| CN109762449A (en) | A kind of bloom self-cleaning powder paint and preparation method thereof | |
| CN108698917A (en) | Transparent base with non-perspective film | |
| JP2015155512A (en) | Coating composition and method for producing the same, water repellant member, and exhaust fan | |
| JP2011184606A (en) | Coating composition, coating film, heat exchanger and air conditioner | |
| JP6843302B1 (en) | Manufacturing method of antifouling member, air conditioner and antifouling member | |
| CN105566953A (en) | Coating composition, antifouling component, air-conditioner and ventilator | |
| WO2020194460A1 (en) | Coating film and forming method therefor, coating composition and production method therefor, and centrifugal blower and air conditioner having said coating film | |
| JP2011115751A (en) | Method for manufacturing antifouling property member and air conditioner | |
| TW202336168A (en) | Water-based paint composition and hardened coating film thereof, and coated article |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |