WO2010016617A1 - 水性プライマー組成物及びそれを用いた塗装方法 - Google Patents
水性プライマー組成物及びそれを用いた塗装方法 Download PDFInfo
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- WO2010016617A1 WO2010016617A1 PCT/JP2009/064280 JP2009064280W WO2010016617A1 WO 2010016617 A1 WO2010016617 A1 WO 2010016617A1 JP 2009064280 W JP2009064280 W JP 2009064280W WO 2010016617 A1 WO2010016617 A1 WO 2010016617A1
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- 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
- C09D123/00—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers
- C09D123/02—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/24—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials for applying particular liquids or other fluent materials
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1806—C6-(meth)acrylate, e.g. (cyclo)hexyl (meth)acrylate or phenyl (meth)acrylate
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- C09D123/00—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers
- C09D123/02—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D123/04—Homopolymers or copolymers of ethene
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- 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
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- 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
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/062—Copolymers with monomers not covered by C09D133/06
- C09D133/066—Copolymers with monomers not covered by C09D133/06 containing -OH groups
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- 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
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
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- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/06—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
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- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
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- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/002—Priming paints
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- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
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- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
- C09D5/028—Pigments; Filters
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- 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
- C09D5/24—Electrically-conducting paints
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/02—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/50—Multilayers
- B05D7/56—Three layers or more
- B05D7/57—Three layers or more the last layer being a clear coat
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
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- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
- C08F220/286—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety and containing polyethylene oxide in the alcohol moiety, e.g. methoxy polyethylene glycol (meth)acrylate
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- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
- C08F220/287—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety and containing polypropylene oxide in the alcohol moiety
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- C08L2201/00—Properties
- C08L2201/50—Aqueous dispersion, e.g. containing polymers with a glass transition temperature (Tg) above 20°C
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- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
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- C08L23/12—Polypropene
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- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
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- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
Definitions
- the present invention relates to a method using an aqueous ply that is excellent in adhesion to plastic and can be formed with excellent finish and water without being subjected to any appreciable wear.
- Plastics such as poi are often used in parts such as outside the vehicle and home appliances. These are often listed with plies containing chlorinated bores, etc., in order to improve their adhesion to molding. This ply has a variety of properties such as
- the agent has been used, but in recent years it has become more water-based in terms of health and safety and environmental conservation.
- the above-mentioned body usually has a body of approximately c, it is difficult to directly charge the material using the static electricity which is excellent in the plastic ratio.
- the material for coloring is electrostatically charged (for example, 6 reports, International Publication No. WO27070432, etc.).
- the 0 296 720 report proposes a three-toe formula including painting a water-based ply, coloring, and yellowing in order.
- water-based ply is used in the wet-out type, water-based ply, It is necessary to prepare for a few minutes before entering the course.
- the present inventors have found that the above objective can be achieved by using an aqueous ply having a specific amount of a specific distate, and has completed the light.
- R R2 independently represents a hydrogen atom having a prime number of 4 to 8
- R 3 represents an akin tomb of 2 to 4, and is a number of 3 to 20, even if the R 3 are the same as each other May be different
- the aqueous ply is characterized in that the content of the composition () is within the range of ⁇ 5 with respect to 00 of the component () and the component ().
- Poofine () modified with water is dispersed in water.
- Saturation power Bon water body is a combination of a small number of species selected from the group of prime numbers 2 to 0, especially 2 to 4, such as chin, puppy, chin, and xeno. Furthermore, the physics obtained by squeezing the saturating force (e.g., (meth) acrylic, ii,, itanoic acid, etc.) with a prime number of 30, especially 48, is preferred. Saturation force It can be obtained by using an anhydride of boric acid according to a method known per se, and in particular, it is preferable that in is modified with water. Saturation power Bonn is not strictly limited by the amount of grafted water, but can vary depending on the physical properties desired for formation, but is generally preferred to be ⁇ 20, based on the amount of poffin. • 5 5, more preferably 2 to 0
- Saturated carbon aquatic body () is a polymer that can be used for sighting by polymerizing in particular because of the narrow distribution of the resulting polyol and excellent random polymerizability. It is preferred that Gustite is of the same kind (gucite), and among gusset media, sens is particularly preferred, metase, usually conjugate five
- Ce bis (quanta) body and its conductor
- Ce which is a compound containing at least one temperament 4 6 8 group transition compound or group 3 rare earth, can activate this, such as anoxa It is obtained by combining a promoter and an organic compound such as methylum.
- Poi can be produced by a method known per se, for example, by continuously adding an axium system while supplying hydrogen such as propylene to the reactor. .
- the saturation force water body () may be further actuated as necessary.
- the polymerizable saturated atom that can be used for the acrylic property include meth (meth) acrylic, cis (meta) act, pi (meta) act, chi () act, (meta) act, and quasi (meta).
- metala) actic acid axe (meta) act, guzzi (meta) act, 2 ⁇ ⁇ (meth) act, (meth) acrylate, () act, etc., and chin, etc. are listed, and these can be used alone or in combination of two or more.
- (meta) act means an act or tact
- (meta) act means an act or tact
- the unsaturated law, water and water reacts with the group in the boy, for example, (meth) Akguji, etc.
- Introducing, then, at least some other species, an unsaturated force introduced with a polymerizable group, a bon-bore, and a copolymerization method is 3 or less, in particular based on the amount of denatured boy () obtained, in particular from ⁇
- the range of 5 to 5 is desirable.
- the above-mentioned saturation force water boin () is formed by a compound having a poxyquine chain, if necessary, in terms of formability, wettability, and hotness. It may be denatured.
- Examples of Okiaki in a compound having a oxyalkyl chain include, for example, Bookichi, Polyoxypropyl, Polyoxy.
- the compound having a poxy chain usually has an average molecule within a range of 40 to 300, preferably 500 to 2,000.
- the average molecular weight is smaller than 400, the result of hydrophilicity cannot be fully exerted, and (especially water resistance) may be adversely affected. Therefore, the solution becomes worse and it is handled.
- modification with a compound having a poxyquine chain can be accomplished by reacting a compound a) having a hydroxyl group at one end with an unsaturated force bohydrate.
- the reaction can be carried out by reacting (b) having a polymerizable saturated group at one end and an oxy chain.
- It has an acid group at one end and has a hydrophobic chain
- (a) includes, for example, Oki Aki Aki Oki Polki Axia such as Poly-Oxide Defote, Polio-Cing Ste-Occhi A-kin, Achia Canoa
- Examples include Iki Akiaki, etc., which can be used alone or in combination of two or more.
- Saturation power Bohydrate Boin A compound having a hydroxyl group at one end and an oxyquine chain (a), for example, heating an unsaturation power bohydrate polyoly at a temperature of 80 ° C.
- the compound (a) can be added, and a basic substance can be added and heated as necessary.
- the range of 0 to 50, particularly 0 to 5 to 25 is generally desirable for the unsaturated power of bodily polyol 10 of compound (a).
- Examples of (b) having a saturated saturated group at one end and a polyoxy chain are: Pog (meth) act, Boppig (meta) act, Booki mechite (meta ) ACT, BOOKUPIPIMETE (META) ACRY, BOOKICHILAUTE (META) ACACT, POLYOCHITETE (META) ACRYLATE, POLOOKICHILAUTE INSTE These can be used alone or in combination of two or more.
- unsaturated power Bon water polyfin is heated at a temperature of 80 to 20 ° C., In the same way as described above, it has reactivity to the grave in the unsaturated power bon water body buffy, for example, (meta) agge, (meta) axe 2
- Etc. and if necessary, add a polymerizable substance and add a polymerizable saturated group to the modified body first, then there This can be done by adding (b), starting polymerization as necessary, and heating.
- the range of 0 to 5 to 50, especially 0 to 5 to 25, is desirable for the unsaturated force of the compound (b), which is 100 for the water body.
- Bofinization can be performed, for example, by blowing a dispersed gas of polio or its properties, and can be within the range of 50 to 20 ° C of the reaction.
- the salt content in the element of the boiler () can be changed according to the physical properties desired for the element of the element, but it is based on the amount of the element of the polyol. In general, under 35, especially 0 30, more particularly 2-25
- Saturation power bodily polyphenols () are particularly suitable to have pupi as a polymerizing position, and the amount fraction of propylene in the saturation power bovine water () is From the standpoint of segregation and formation, it is usually preferable to be within the range of 0 ⁇ 50 ⁇ 99, especially 0 ⁇ 6 to 0 ⁇ 97, more particularly 0 ⁇ 70 ⁇ 95.
- the unsaturation force obtained from the above is generally less than 20oC, preferably 50 to 00C, more preferably 60 to 9ooC, generally 3000 000. May have an average molecular weight (w) within the range of 500 to 50 000, more preferably 700 to 20,000. If the point of buffy and the average molecule are removed from these ranges, the ability to form, the ability to form and the adhesion to the top, etc., are reduced.
- the melting point and the amount of heat release were measured by heating the modified body 2 from 0 C to 50 C in C minutes using a capacity setting device SC 520 (trade name, manufactured by Seiko Kogyo Co., Ltd.). Is obtained. If the amount of heat loss is calculated, the measurement fee is 2 o
- the calorific value may be measured by the above method for 2 or more.
- the above-mentioned saturation force water body () generally has a mass average molecular weight (w) of 5 to 0, especially 2 It is desirable to be within the range of 0 to 3 ⁇ 5, and in particular, 2 ⁇ 0 to 3 ⁇ .
- the dispersion () of the modified oil used in the art can be obtained by dispersing the above-mentioned saturated power bon water body () in an aqueous solution, for example, Io.
- the tomb part in the unsaturated power bon water body () can be neutralized entirely with a compound or dispersed using an emulsifier.
- the compound or emulsifier is not used or their For this purpose, it is possible to disperse the modified polyol () in aqueous form.
- the dose is usually within the range of ⁇ to the group in the above-mentioned saturating water bath ().
- agent examples include Boochi no Oite, Poochi no steate, Boochi no Lautee, Pochichi Trite, Oki Chifute, Polyochitete, Polyochitete, Poochitin NORAT, BOOKICHI NOSTEAT, BOOKICHINOTO,
- Examples include anodic agents such as norato, no steato, tautoto, and vouchichinsonolato. Axhoshon, axenshon, and sodium oxalates such as acetic acid.
- polyoxyalkylating agents having an oxyquine group such as an opoxykipin group in the child and a reactive agent having an ao polymerizable saturated group in the child Can also be used. These can be used alone or in combination of two or more.
- the dosage of the agent is the saturation power
- Water and water-based aqua Contains light ply, water-based water () or water-based water (2).
- Uta () is a water-soluble or water-dispersible compound that has a combination of urea in the molecule, and includes acid-soluble emulsifiers and water-soluble fats. Is preferred. Utandisjo is usually a disjojo that is obtained by forcing or automating the emulsifier while pre-dio-isocyanate and, if necessary, Utamppo obtained by thiacan reaction are dispersed in water. is there.
- Examples of the case of U (B) include the Te system, the carbon system, and the Ste system. From the viewpoint of these aqueous properties, the Te system is desirable.
- the aqueous water () may contain a hydroxyl group.
- Acrylic (2) usually has a mass-average molecular weight of 5 which is obtained by copolymerization of water-soluble saturated compounds such as strength-compatible compounds and other polymerizable saturated compounds.
- a soluble oil in the range of 000, preferably 5,000 000, an acrylate on the mass average 50 000, and preferably 000 000 can be used. This is a value calculated based on the average molecular weight of the mass average molecular weight polystyrene determined by using photon chromatography, using tetradorolane as the average molecular weight.
- C8 20GP C (trade name) can be used as gammagraphy,
- Se G 400 X Se G 300O X, Se G 250O X, Se G O X
- compatibility saturation examples include (meta) ac, kuto, in,, ita, and these Other examples of the water-soluble, saturated aqueous solution include dialkyl acids such as poly (meth) acrylate and boppig (meth) aqua.
- Rholide 2 (metaquinium) chitomethiaumoid, etc.
- Acaturation saturated No. 4 Aum cavity Saturation no.
- Other polymerizable saturated groups include, for example, meth (meth) act, h (meta) act, if pup (meta) act, if one (meth) act, 2
- Cactic acid such as Ki (meth) acrylate, Ku (meth) acrylate, Lau (meth) acrylate, Isovo (meth) act, etc. ) Acryte, 2 or 3 pup (meta) act, 4 (meth) act, etc.Acactic acid axetag (meta) act, act, acrid, ste, Viton, Bi, Bichloride, 6-Xiadiodiact.
- Polymerization of the compound is not particularly limited, and can be performed by a method known per se, for example, by a water-soluble polymerization method, and the action is legal. Can be done.
- the acrylic (2) is an acrylic obtained by combination, it is a multi-layered particulate powder obtained by combining water and a chemical agent in multiple stages. Moyo.
- a basic substance such as a group derived from the hydrophilic compatibility in the aqua (2).
- the basic substance that can be used in this case is preferably water-soluble.
- Am-Achia, Chia, Pupi, Chia, Methia, Tochitia, Tochia, Chia Examples include dian,, metitanoa, metitanoa, tanoan, totanoa, sopnoa,? Anomethino and these may be used alone or in combination of two or more. it can.
- Aque is desirable to contain a hydroxyl group, and in terms of its ability to disperse in water and formability, it generally has an acid group within the range of 20 20, especially 2 to 5 O, generally 0 O, especially It is desirable to have a value in the range of 0-7 OO.
- the component (B) with the sex dispersion () and () is generally within the range of 90.70, particularly 585 to 6535, and more particularly 20 80 60.40. If it is outside this range, it is not preferable because the formability of the material to be formed, wateriness, and evaporation deteriorate.
- Ste compound (C) is generally within the range of 90.70, particularly 585 to 6535, and more particularly 20 80 60.40. If it is outside this range, it is not preferable because the formability of the material to be formed, wateriness, and evaporation deteriorate.
- R R2 independently represents a hydrogen atom having a prime number of 48
- R3 represents an alkyl group having a prime number of 24, is a number of 3 to 20, and the R3s may be the same or different from each other Even
- the hydrogen fluoride represented by R or R2 is preferably an acyl group having 5 to 9 carbon atoms, more preferably an acyl group having 5 to 9 carbon atoms, and an aryl group having 6 to 8 carbon atoms. Ki group is more preferred.
- R R2 is a hex group with a prime number of 68, it is possible to give excellent formation when formed after storing the material for a comparative period.
- R3 is preferably h, and more preferably is a number from 4 to 0.
- the compound (C) can be obtained, for example, by subjecting a carboxy group having 48 polyoxyalkyl atoms having two terminal acid groups to a ste reaction.
- Poki Agri can include bolting, polypiping, rocking polymer of potigliping pigs, potting, etc. I prefer that.
- These polyoxyalkyls preferably have an average molecular weight within the range of about 2 to 800, particularly about 5600, and more particularly about 20 to 00, from the viewpoint of aqueous properties.
- Examples of the carbohydrate having the prime 4 to 8 hydrides include, for example, ta, xa, 2 butane, 3 metha, benzoic acid, cloxa cabo, puta, 2 tin, 3 tin, octa, 2 Kissa, 4 Chissa, Nan, 2 Peta, Deca, 2 Chiocta, 4 Octa, Deca, Kisadeka, Octadeca And so on. Of these, Kissa, Puta, 2 Peta, 3 Peta, Octa, 2 Thixa, 4 Thixa, Na, 2 Peta, Deca,
- Octa, 4-octanoic acid, etc. have 5 to 9 prime alk groups, carboxylic acids are preferred, and penta-, ta-, 3-ta, octane, 2-xan, 4-xanthana, 2-thiptaic acid, etc.
- a carboxylic acid having an alk group is preferred, and a carboxylic acid having a prime number of 6 to 8 such as tantalum, 3 chipeta oxa, 4 thixa, and 2 ptacid is more preferred.
- Kingli Ste-reaction with the above-mentioned nobobo can itself be carried out by an intelligent method.
- VOKIA KIG Each of the above-mentioned novo acids can be used alone or in combination of two or more.
- the compound (C) to be obtained has a property generally within the range of about 320, particularly about 40,800, and more particularly about 57, from the viewpoint of ascending property and aqueous property.
- the amount of the compound (C) in the bright ply is generally ⁇ 5, preferably 2 ⁇ 3 ⁇ 5, more preferably 3 ⁇ 2 relative to the component ()
- genus powder such as bonak, cabotive, caboai, caboikui, etc., powders, blackfish, glaphite, aum, etc., and anti-anti Oxide oxide on the surface of the pigmented squid surface coated with tin oxide on the whisker surface of titanium, anti-oxide, indium oxide, indium oxide, carbographite, etc.
- Pigment coated with a material Titanium oxide The material containing tin oxide and containing on the surface, etc. are mentioned, and these can be used alone or in combination of two or more. These especially conductive bon can be used suitably.
- the amount of () is the amount of () ()
- the dose is usually within the range of ⁇ 30, especially 3 ⁇ 250, and more particularly 5 ⁇ 80.
- the dose is usually within the range of ⁇ 30, especially 3 ⁇ 250, and more particularly 5 ⁇ 80.
- the dose is usually within the range of ⁇ 30, especially 3 ⁇ 250, and more particularly 5 ⁇ 80.
- a clear ply for example,
- Dispersion (), (), compound (C) () can be prepared by following conventional methods and diluting with body, for example, Io water.
- the bright ply can contain crosslinks if necessary.
- examples thereof include an anoic acid and / or a (c) isocyanate, which can react with the hydroxyl acid contained in the above ().
- a compound capable of reacting with the dispersion () of the modified body may be cross-linked.
- Bright ply and if necessary, it can contain agents such as curing agent, organic agent, and surface agent.
- the share of is usually 3
- plastics examples include plastic products used in parts of moving parts such as motors, spoilers, gears, and hoods.
- the quality of plastics such as For example, a point of 2 or more primes, such as Xe, is particularly suitable, but other than that, botane, S fat, cotton fat, A clear ply can be applied to the ad.
- plastics can be degreased and washed with water using a method known per se prior to wearing the clear ply.
- plastic is usually 20 u dry, preferably 2 to 0, and more preferably 3 to 7 in order to ensure that the fee increases quickly. It is preferable to use asp, asp, and hair. , Get, If necessary, it can be set at room temperature for about 30 to 60 hours, or about 40 to 80 degrees Celsius, and can be reserved for about 60 to 60 hours, or 60 to 40 ° C, preferably 7 to 60 ° C. It can be heated by 20 to 40 degrees at a temperature of 20 ° C. However, in the morning, it is possible to carry out the apparel without painting the bright ply.
- the later fee can be determined as follows. Apply the same material as above on a fixed area of Aum foil, collect it later, and immediately fold the Aum foil to quickly measure the weight without causing further evaporation. . Then, the amount is measured in the same way as the thermosetting of the aluminum foil. The amount of charge is calculated from these amounts and the predetermined amount of Aum.
- Coloring materials can be used alone as materials, or materials and materials can be ordered sequentially. Also, above For example, a white material and a material may be sequentially mounted on the ply.
- Materials known per se can be used, usually organic materials and / or water, mainly containing coloring pigments, brilliants, materials, etc., and fats, cross-linking agents, etc. Can be used.
- Examples of the material used for the material include fats such as an axostapse and an axylate, which are more reactive than a hydroxyl group, a polyoxy group, or a lano group. In addition, it reacts with the above-mentioned functionalities and reacts with anodic (such as rubber and fat) iso-and
- it may contain a constitutional material, curing, ultraviolet rays, ointment, oxidation, extinction, wax, preservative and the like.
- the above-mentioned or cured ply usually 5 to 5, preferably 5 to 30 and more preferably 0 to 20 and can be obtained. It can be set for about 6 hours, or can be reserved for about 6 hours at a temperature of about 40 C, or it can be heated for about 40 to 40 C, preferably about 8 to 2 oC for about 20 to 40 C. You can. In the light, it is particularly preferable to carry out the dressing next without curing the colorant to the paint.
- clearing materials examples include fats, cross-linking agents, etc., and agents and water.If necessary, UV, light, curing, oxidants, oxidation, extinction, wax, etc.
- the organic compound it is possible to use a water-based curable coating that is clear enough to be formed as a lower layer through the formed coating.
- there are various types of reactivity such as hydroxyl group, force, lano, and poxy group.
- Examples thereof include fat and the like, and particularly, hydroxyl group is preferable.
- Examples of such compounds include lanthanides, fats, (c) isocyanato compounds, pocket compounds, powerful compounds, acid hydrates, and asyla compounds that react with these.
- a polyisoamine compound is preferred.
- the clearing material is converted or cured, and is usually placed in the range of 0 to 50, preferably 2 to 40, and is obtained at room temperature for about 60 to 60 minutes, if necessary. Or after preheating at a temperature of about 40 to 8 C for about -6 hours and then heating for about 2 to 4 at a temperature of about 6 to C, preferably 7 to 2 C.
- plies (2) to (3) were obtained. It is a solid display, and () to (8) in it are as follows.
- R R2 is a 2-tin group
- R3 is a tin group, and is 578.
- the material after the water-based ply is first coated on the same area of the aluminum foil with the same material in the above-mentioned bus, collected later, and immediately folded into the aluminum foil. Measure the weight quickly without causing any problems. Then, the aluminum foil is opened and heated at 80oC for 30 minutes, and then the weight is measured. The amount of these substances, the amount of Aum, and the price of the charge were calculated.
- X is above 000O.
- the top is both good and shiny
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
Claims
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010523920A JP5649447B2 (ja) | 2008-08-08 | 2009-08-06 | 水性プライマー組成物及びそれを用いた塗装方法 |
| US13/057,196 US20110135936A1 (en) | 2008-08-08 | 2009-08-06 | Water-based primer composition and coating method using the same |
| CN2009801310074A CN102119195B (zh) | 2008-08-08 | 2009-08-06 | 水性底漆组合物以及使用该组合物的涂覆方法 |
| GB201100954A GB2474392B (en) | 2008-08-08 | 2009-08-06 | Aqueous primer composition, and coating method using the same |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008-205379 | 2008-08-08 | ||
| JP2008205379 | 2008-08-08 |
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| Publication Number | Publication Date |
|---|---|
| WO2010016617A1 true WO2010016617A1 (ja) | 2010-02-11 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2009/064280 Ceased WO2010016617A1 (ja) | 2008-08-08 | 2009-08-06 | 水性プライマー組成物及びそれを用いた塗装方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20110135936A1 (ja) |
| JP (1) | JP5649447B2 (ja) |
| CN (1) | CN102119195B (ja) |
| GB (1) | GB2474392B (ja) |
| WO (1) | WO2010016617A1 (ja) |
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| WO2011096480A1 (ja) * | 2010-02-05 | 2011-08-11 | 関西ペイント株式会社 | 水性プライマー組成物及びそれを用いた塗装方法 |
| JP2011530393A (ja) * | 2008-08-12 | 2011-12-22 | 関西ペイント株式会社 | 複層塗膜形成方法 |
| JP2013085980A (ja) * | 2011-10-13 | 2013-05-13 | Suzuki Motor Corp | 塗装方法 |
| WO2013191104A1 (ja) | 2012-06-19 | 2013-12-27 | 関西ペイント株式会社 | 水性塗料組成物及びそれを用いた塗装方法 |
| JP2015182392A (ja) * | 2014-03-25 | 2015-10-22 | 旭化成ケミカルズ株式会社 | 成型体 |
| JP2016538370A (ja) * | 2013-11-08 | 2016-12-08 | ダウ グローバル テクノロジーズ エルエルシー | 下塗り剤不要塗料組成物、その製造方法、及びそれを含む物品 |
| JP2018108734A (ja) * | 2016-12-28 | 2018-07-12 | エスケー イノベーション カンパニー リミテッドSk Innovation Co.,Ltd. | 伝導性塗膜 |
| JP2020195944A (ja) * | 2019-05-31 | 2020-12-10 | 関西ペイント株式会社 | プラスチック成形品の塗装方法 |
| US10913868B2 (en) | 2015-01-29 | 2021-02-09 | Kansai Paint Co., Ltd. | Aqueous coating composition |
| JP2021115488A (ja) * | 2020-01-22 | 2021-08-10 | 関西ペイント株式会社 | プラスチック成形品の塗装方法 |
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| DE102011075736A1 (de) * | 2011-05-12 | 2012-11-15 | Siemens Aktiengesellschaft | Elektrisch leitfähiger Lack |
| EP2997083A1 (en) | 2013-05-16 | 2016-03-23 | LORD Corporation | Aqueous conductive coating |
| JP6359284B2 (ja) * | 2014-02-17 | 2018-07-18 | スリーエム イノベイティブ プロパティズ カンパニー | 感圧接着剤 |
| CN106103593B (zh) | 2014-03-12 | 2020-03-10 | 3M创新有限公司 | 导电聚合物材料 |
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| JP7001710B2 (ja) | 2017-04-11 | 2022-01-20 | ダウ グローバル テクノロジーズ エルエルシー | 耐熱性が改善された水性乾燥積層体結合剤 |
| CN115926541B (zh) * | 2022-11-04 | 2023-09-12 | 广东安捷伦新材料科技有限公司 | 一种免火焰处理pp底漆及其制备方法与应用 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001002977A (ja) * | 1999-06-22 | 2001-01-09 | Honda Motor Co Ltd | 自動車内装材用水性塗料組成物 |
| JP2004256577A (ja) * | 2003-02-24 | 2004-09-16 | Dainippon Ink & Chem Inc | ポリオレフィン基材用水性塗料樹脂組成物 |
| JP2004331911A (ja) * | 2003-05-12 | 2004-11-25 | Toyota Motor Corp | ポリオレフィン用水性プライマー組成物 |
| WO2005012449A1 (ja) * | 2003-07-23 | 2005-02-10 | Kansai Paint Co., Ltd. | 白色導電性プライマー塗料組成物及び複層塗膜形成方法 |
| JP2005171024A (ja) * | 2003-12-09 | 2005-06-30 | Kansai Paint Co Ltd | 白色導電性プライマー塗料 |
| WO2007046532A1 (ja) * | 2005-10-18 | 2007-04-26 | Kansai Paint Co., Ltd. | 水性プライマー組成物及びその塗装方法 |
| JP2007238719A (ja) * | 2006-03-07 | 2007-09-20 | Nippon Bee Chemical Co Ltd | 導電性プライマー塗料およびこれを用いる塗膜形成方法 |
| WO2007119760A1 (ja) * | 2006-04-11 | 2007-10-25 | Kansai Paint Co., Ltd. | 水性プライマー組成物 |
| JP2008201882A (ja) * | 2007-02-20 | 2008-09-04 | Kansai Paint Co Ltd | 水性プライマー組成物、及びこの組成物を用いた塗装方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US21742A (en) * | 1858-10-12 | Machine for dressing stone | ||
| US5425969A (en) * | 1992-06-26 | 1995-06-20 | Toyota Jidosha Kabushiki Kaisha | Method of coating articles made of polypropylene with an electrically conductive primer and electrostatically applied overcoat |
| JP2001302985A (ja) * | 2000-04-24 | 2001-10-31 | Kansai Paint Co Ltd | 電着塗料 |
| JP5171261B2 (ja) * | 2005-12-09 | 2013-03-27 | 関西ペイント株式会社 | 水性プライマー塗料組成物 |
| JP2007302709A (ja) * | 2006-05-08 | 2007-11-22 | Kansai Paint Co Ltd | 水性プライマー組成物 |
| CN101117479B (zh) * | 2006-07-31 | 2010-09-22 | 本田技研工业株式会社 | 水性底漆涂料组合物和涂膜形成方法 |
| JP5594931B2 (ja) * | 2006-11-02 | 2014-09-24 | 関西ペイント株式会社 | 水性ベース塗料組成物 |
| CN101020753B (zh) * | 2007-03-19 | 2010-12-15 | 江苏柏鹤涂料有限公司 | 用于聚丙烯底材的水性树脂及水性漆 |
| JP5601760B2 (ja) * | 2007-06-29 | 2014-10-08 | 関西ペイント株式会社 | 水性プライマー組成物、及びこの組成物を用いた塗装方法 |
-
2009
- 2009-08-06 WO PCT/JP2009/064280 patent/WO2010016617A1/ja not_active Ceased
- 2009-08-06 CN CN2009801310074A patent/CN102119195B/zh active Active
- 2009-08-06 JP JP2010523920A patent/JP5649447B2/ja active Active
- 2009-08-06 US US13/057,196 patent/US20110135936A1/en not_active Abandoned
- 2009-08-06 GB GB201100954A patent/GB2474392B/en not_active Expired - Fee Related
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001002977A (ja) * | 1999-06-22 | 2001-01-09 | Honda Motor Co Ltd | 自動車内装材用水性塗料組成物 |
| JP2004256577A (ja) * | 2003-02-24 | 2004-09-16 | Dainippon Ink & Chem Inc | ポリオレフィン基材用水性塗料樹脂組成物 |
| JP2004331911A (ja) * | 2003-05-12 | 2004-11-25 | Toyota Motor Corp | ポリオレフィン用水性プライマー組成物 |
| WO2005012449A1 (ja) * | 2003-07-23 | 2005-02-10 | Kansai Paint Co., Ltd. | 白色導電性プライマー塗料組成物及び複層塗膜形成方法 |
| JP2005171024A (ja) * | 2003-12-09 | 2005-06-30 | Kansai Paint Co Ltd | 白色導電性プライマー塗料 |
| WO2007046532A1 (ja) * | 2005-10-18 | 2007-04-26 | Kansai Paint Co., Ltd. | 水性プライマー組成物及びその塗装方法 |
| JP2007238719A (ja) * | 2006-03-07 | 2007-09-20 | Nippon Bee Chemical Co Ltd | 導電性プライマー塗料およびこれを用いる塗膜形成方法 |
| WO2007119760A1 (ja) * | 2006-04-11 | 2007-10-25 | Kansai Paint Co., Ltd. | 水性プライマー組成物 |
| JP2008201882A (ja) * | 2007-02-20 | 2008-09-04 | Kansai Paint Co Ltd | 水性プライマー組成物、及びこの組成物を用いた塗装方法 |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011530393A (ja) * | 2008-08-12 | 2011-12-22 | 関西ペイント株式会社 | 複層塗膜形成方法 |
| WO2011096480A1 (ja) * | 2010-02-05 | 2011-08-11 | 関西ペイント株式会社 | 水性プライマー組成物及びそれを用いた塗装方法 |
| JPWO2011096480A1 (ja) * | 2010-02-05 | 2013-06-10 | 関西ペイント株式会社 | 水性プライマー組成物及びそれを用いた塗装方法 |
| JP2013085980A (ja) * | 2011-10-13 | 2013-05-13 | Suzuki Motor Corp | 塗装方法 |
| US9580619B2 (en) | 2012-06-19 | 2017-02-28 | Kansai Paint Co., Ltd. | Aqueous coating composition and coating method using same |
| JPWO2013191104A1 (ja) * | 2012-06-19 | 2016-05-26 | 関西ペイント株式会社 | 水性塗料組成物及びそれを用いた塗装方法 |
| WO2013191104A1 (ja) | 2012-06-19 | 2013-12-27 | 関西ペイント株式会社 | 水性塗料組成物及びそれを用いた塗装方法 |
| JP2016538370A (ja) * | 2013-11-08 | 2016-12-08 | ダウ グローバル テクノロジーズ エルエルシー | 下塗り剤不要塗料組成物、その製造方法、及びそれを含む物品 |
| JP2015182392A (ja) * | 2014-03-25 | 2015-10-22 | 旭化成ケミカルズ株式会社 | 成型体 |
| US10913868B2 (en) | 2015-01-29 | 2021-02-09 | Kansai Paint Co., Ltd. | Aqueous coating composition |
| JP2018108734A (ja) * | 2016-12-28 | 2018-07-12 | エスケー イノベーション カンパニー リミテッドSk Innovation Co.,Ltd. | 伝導性塗膜 |
| JP7067832B2 (ja) | 2016-12-28 | 2022-05-16 | エスケー イノベーション カンパニー リミテッド | 伝導性塗膜 |
| JP2020195944A (ja) * | 2019-05-31 | 2020-12-10 | 関西ペイント株式会社 | プラスチック成形品の塗装方法 |
| JP7099994B2 (ja) | 2019-05-31 | 2022-07-12 | 関西ペイント株式会社 | プラスチック成形品の塗装方法 |
| JP2021115488A (ja) * | 2020-01-22 | 2021-08-10 | 関西ペイント株式会社 | プラスチック成形品の塗装方法 |
| JP7272971B2 (ja) | 2020-01-22 | 2023-05-12 | 関西ペイント株式会社 | プラスチック成形品の塗装方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20110135936A1 (en) | 2011-06-09 |
| CN102119195B (zh) | 2013-10-23 |
| GB2474392A (en) | 2011-04-13 |
| GB201100954D0 (en) | 2011-03-02 |
| JP5649447B2 (ja) | 2015-01-07 |
| CN102119195A (zh) | 2011-07-06 |
| JPWO2010016617A1 (ja) | 2012-01-26 |
| GB2474392B (en) | 2012-09-05 |
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