WO2006033208A1 - タイヤコーティング剤セット及びタイヤコーティング方法 - Google Patents
タイヤコーティング剤セット及びタイヤコーティング方法 Download PDFInfo
- Publication number
- WO2006033208A1 WO2006033208A1 PCT/JP2005/014935 JP2005014935W WO2006033208A1 WO 2006033208 A1 WO2006033208 A1 WO 2006033208A1 JP 2005014935 W JP2005014935 W JP 2005014935W WO 2006033208 A1 WO2006033208 A1 WO 2006033208A1
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- WIPO (PCT)
- Prior art keywords
- liquid
- tire
- black
- hydrogen
- group
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
- C08L51/085—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds on to polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
-
- 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
- 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
- C09D151/003—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 macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
-
- 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
- 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
- C09D151/08—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 macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C09D151/085—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 macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds on to polysiloxanes
-
- 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
- B05D2201/00—Polymeric substrate or laminate
-
- 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
- B05D7/52—Two layers
Definitions
- the present invention relates to a tire coating agent set and a tire coating method for projecting a black surface of a tire such as an automobile, a bicycle, a motorcycle, or a black bumper.
- silicone oil is the main component, it is generally used because it has excellent gloss on the finished surface, and most of it is a fluid with a high boiling point. In order to remove the attached contaminants, the finished surface with poor dryness will remain sticky, and the contaminants will be more likely to adhere, and the anti-contamination effect (antifouling) will not be exhibited. Even if we try to wash with water using detergents containing surfactants, there is a problem that due to silicone oil and pollutants, the detergents do not foam, and even the sponge that is a cleaning tool is stained black.
- Patent Document 1 proposes a tire squeezing agent obtained by emulsifying and dispersing wax, organosiloxane oil, carbon black, and polyurethane resin in water. This tire finish can reduce the stickiness of the finished surface, but it must be wiped off after application, and the gloss after finishing is inferior to that based on silicone oil. There is a problem.
- Patent Document 2 proposes a tire treading agent in which a plasticizer is blended with an acrylic ester polymer and / or a methacrylic ester polymer having a glass transition temperature of 0 to 50 ° C. ing.
- this tire squeezing agent forms a water-insoluble coating film on the tire surface. If a crack occurs or the coating film deteriorates over time, it is difficult to remove it easily by washing, and it is difficult to remove it completely.
- the new paint is applied on top of the film, the appearance gradually deteriorates, and conversely, when it is desired to reduce the gloss, it can be easily lost. There are problems such as inability to
- Patent Document 3 includes a water-dispersible or water-soluble rosin component and a modified silicone having a hydrophilic group as a plasticizer component that is compatible with the rosin component, and can be washed with water.
- a water-dispersible or water-soluble rosin component and a modified silicone having a hydrophilic group as a plasticizer component that is compatible with the rosin component, and can be washed with water.
- Protective glazing agents for tires that form a good coating have been proposed.
- Patent Document 1 Japanese Patent Application Laid-Open No. 8-239629
- Patent Document 2 JP 2000-144038
- Patent Document 3 Japanese Patent Laid-Open No. 2002-256225
- Patent Document 4 Japanese Patent Laid-Open No. 5-230161
- Patent Document 5 JP-A-7-196975
- the tire squeezing agent disclosed in Patent Document 3 contains black matter such as carbon black! /,!, So it is poor in black squeezing effect.
- the present invention has been made in view of the above-mentioned problems of the prior art, and the problem to be solved by the present invention is to impart black glaze to black surfaces of automobile tires, black bumpers and the like.
- the present invention also provides a tire coating that can be cleaned with a general car shampoo, without causing stickiness, dirt, or cracking of the coating.
- the present inventors have formulated a tire coating agent by separating it into a first liquid obtained by dispersing a black product in a dispersion medium and a second liquid for brewing, and The present inventors have found that these problems can be solved by using a liquid obtained by dispersing silicone-grafted acrylic resin in a dispersion medium as the second liquid, and have completed the present invention.
- the tire coating agent set of the present invention is obtained by dispersing a black product in a dispersion medium. And a second liquid obtained by dissolving a silicone-grafted acrylic resin in a solvent.
- the first liquid obtained by dispersing a black product in a dispersion medium is applied, and a silicone-grafted acrylic resin is used as a solvent on the black film formed thereby. It is characterized by applying a second liquid which is dissolved.
- a black film is formed on the black surface of an automobile tire, a black bumper or the like, and by applying the second liquid thereon, the surface becomes sticky while giving gloss. It is possible to impart a soil adhesion prevention performance. It can be cleaned with a common car shampoo without causing cracks in the coating.
- the silicone-grafted acrylic resin is an acrylic resin, acrylate ester resin, methacrylic acid resin or methacrylic acid ester resin and a component obtained by drafting silicone. It contains rosin.
- the silicone-grafted acrylic resin is represented by the following general formula (1):
- R 1 is hydrogen or a methyl group
- R 2 is a divalent hydrocarbon group having 1 to 12 carbon atoms which may be interrupted by an oxygen atom
- R 3 is a monovalent hydrocarbon group having 1 to 6 carbon atoms
- m is 1 , 2 or 3
- n represents an integer of 3 to 200.
- Preferred to have a structure of
- the silicone-grafted acrylic resin has the following general formula (2)
- R 1 is hydrogen or a methyl group
- R 2 is a divalent hydrocarbon group having 1 12 carbon atoms which may be interrupted by an oxygen atom
- R 3 is a monovalent hydrocarbon group having 16 carbon atoms
- R 4 is hydrogen or A methyl group
- m is 12 or 3
- n is an integer of 3 200.
- Preferred to have a structure of
- the silicone-grafted acrylic resin has the following general formula (3)
- R 1 is hydrogen or a methyl group
- R 2 is a divalent hydrocarbon group having 1 12 carbon atoms which may be interrupted by an oxygen atom
- R 3 is a monovalent hydrocarbon group having 16 carbon atoms
- R 4 is hydrogen or Methyl group
- R 5 is hydrogen or methyl group
- R 6 is other alkyl group or functional group-containing alkyl group
- m is 12 or 3
- n is an integer of 3200.
- Preferred to have a structure of
- the second liquid has the following general formula (1)
- R 1 is hydrogen or a methyl group
- IT is a divalent carbon atom of 1 12 which may be interrupted by an oxygen atom.
- a hydrocarbon group R 3 is a monovalent hydrocarbon group having 1 to 6 carbon atoms, m is 1, 2 or 3, and n is an integer of 3 to 200.
- R 1 is hydrogen or a methyl group
- R 2 is a C 1-12 divalent hydrocarbon group that may be interrupted by an oxygen atom
- R 3 is a C 1-6 monovalent hydrocarbon group
- R 4 is Hydrogen or methyl group
- m is 1, 2 or 3
- n represents an integer of 3 to 200.
- a silicone-grafted acrylic resin having the following structure and a resin having the following general formula (4) may be mixed and dispersed.
- R 4 represents hydrogen or a methyl group
- R 5 represents hydrogen or a methyl group
- R 6 represents another alkyl group or a functional group-containing alkyl group.
- a black surface such as an automobile tire or a black bumper is imparted with black glaze to regenerate like a new tire, while stickiness, adhesion of dirt, cracking of a coating film. It is possible to provide a tire coating that can be washed with a general car shampoo.
- the black material contained in the first liquid includes a black pigment or a black dye.
- Black pigments include carbon black, garlic black, synthetic iron oxide (TAROX, etc., manufactured by Titanium Industry Co., Ltd.), ivory black (bone charcoal), peach black (vegetable charcoal), temp black (oil charcoal), vitume bitumin vitume ( Asphalt) and the like.
- inexpensive and non-toxic carbon black is preferable.
- black dyes include orthoaminophenol and paraphenol-diamine.
- the dispersion medium contained in the first liquid may be any alcohol-based dispersion medium, silicone, or the like, as long as it is a liquid that disperses a black pigment at room temperature or a liquid that dissolves a black dye and has volatility.
- examples thereof include a system dispersion medium, a petroleum system dispersion medium, a glycol system dispersion medium, and an aqueous system dispersion medium.
- examples of the alcohol-based dispersion medium include methanol, ethanol, 1-propanol, 2-propanol, and the like.
- silicone-based dispersion medium examples include dimethyl silicone having a kinematic viscosity at 25 ° C of 0.65 to 2 mm 2 / s, 4 to 6
- petroleum-based dispersion media include non-raffinic hydrocarbons such as pentane, hexane, and heptane, industrial gasoline, kerosene, mineral split, isoparaffin, and cycloparaffin.
- glycol-based dispersion medium include ethylene glycol, propylene glycol, trimethylene glycol, triethylene glycol, 1,4-butanediol, and 1,5-pentanediol.
- water may be used for hydrophilic carbon black.
- Water containing a dispersant for each of surfactants such as a cation, a cation, a non-ion and an amphoteric surfactant may be used for a normal hydrophobic carbon black.
- surfactants such as a cation, a cation, a non-ion and an amphoteric surfactant
- water containing a dispersant for a non-active agent is preferable in terms of ease of use.
- polyoxyethylene cetyl ether polyoxyethylene glycol ether, polyoxyethylene stearyl ether, polyoxyethylene lauryl ether, polyoxyethylene isocetyl ether, polyoxyethylene Isostearyl ether, polyoxyethylene octyldodecyl ether, polyoxyethylene ethyl ether, polyoxyethylene decyl tetradecyl ether, polyoxyethylene cholesteryl ether, polyoxyethylene oleyl cetyl ether, polyoxyethylene isodecyl ether, polyoxy Higher alcohols (AE) with ethylene oxide such as ethylene tridecyl ether and polyoxyethylene lanolin alcohol ether, polyoxyethylene.
- AE Higher alcohols
- Carboxymethyl propylene decyl ether polyoxyethylene styrenated Ether-based non-active agents such as alkylated phenyl ether, polyoxyethylene alkylene alkyl ether, polyoxyethylene alkyl ether, polyoxyethylene alkyl amine ether, polyoxyethylene alkyl ether, polyoxyethylene alkyl ether, alkyl glyceryl ether, etc.
- Polyoxyethylene glycol fatty acid ester Polyoxyethylene hydrogenated castor oil, alkylphenol (APE) with ethylene oxide, polyoxypropylene glycol with polyoxyethylene, glycerin fatty acid ester, propylene glycol fatty acid ester, Sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol tetraoleate, alkanolamine fatty acid condensation
- fluorinated hydrocarbon group-containing nonionic surfactants and the like can be suitably used.
- tires that do not adversely affect the tire such as cracks are preferred.
- 2-propanol, the above-mentioned silicone dispersion medium, heptane, water containing the above ether-based non-active agent, etc. are preferred.
- the first liquid can be made into an OZW type or WZO type emulsion by adding various binder components such as wax and rosin and an emulsifying agent.
- specific silicone-grafted acrylic resins contained in the second liquid include, for example, the following monomers and other radicals as disclosed in Patent Document 4 and Patent Document 5: It can be obtained by radical polymerization with a cal-polymerizable monomer.
- examples of the solvent contained in the second liquid include an alcohol dispersion medium, a silicone dispersion medium, a petroleum dispersion medium, a glycol dispersion medium, and an aqueous dispersion medium.
- examples of the alcohol-based dispersion medium include methanol, ethanol, 1 propanol, and 2-propanol V
- examples of the silicone-based dispersion medium include dimethyl silicone having a kinematic viscosity at 25 ° C of 0.65 to 2 mm 2 / s.
- Examples of the petroleum-based dispersion medium include paraffinic hydrocarbons such as pentane, hexane, and heptane, industrial gasoline, kerosene, mineral split, isoparaffin, and cycloparaffin.
- Examples of the glycol dispersion medium include ethylene glycol, propylene glycol, trimethylene glycol, 1,4-butanediol, and 1,5-pentanediol.
- the aqueous dispersion medium may be water containing water-containing surfactants such as water, cation, nonone and amphoteric surfactants. Of these, water containing a dispersant for a non-active agent is preferable in terms of ease of use.
- polyoxyethylene cetyl ether polyoxyethylene glycol ether, polyoxyethylene stearyl ether, polyoxyethylene lauryl ether, polyoxyethylene isocetyl ether, polyoxyethylene isoester Stearyl ether, polyoxyethylene octyldodecyl ether, polyoxyethylene behenyl ether, polyoxyethylene decyl tetradecyl ether, polyoxyethylene cholesteryl ether, polyoxy Higher alcohols (AE) with ethylene oxide such as ethyleneolyl cetyl ether, polyoxyethylene isodecyl ether, polyoxyethylene tridecyl ether, polyoxyethylene lanolin alcohol ether, polyoxyethylene 'polyoxypropylene decyl ether, Ether-type polymers such as polyoxyethylene styrenated ether, polyoxyethylene alkylene alkyl ether, polyoxyethylene alkyl ether, polyoxyethylene alkyl amine
- polyoxyethylene glycol fatty acid ester polyoxyethylene hydrogenated castor oil, key oxide with ethylene oxide Phenol (APE), polyoxypropylene glycol with polyoxyethylene, glycerin fatty acid ester, propylene glycol fatty acid ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol tetraoleate, alkanolamine fatty acid condensate
- fluorinated hydrocarbon group-containing nonionic surfactants and the like can be suitably used. In particular, those that do not adversely affect the tire such as cracking are preferred.
- 2-propanol, the above-mentioned silicone-based dispersion medium, heptane, water containing the above ether-based non-active agent, and the like are preferred.
- the first liquid and Z or the second liquid may further improve performances such as coating surface protection and refreshment during use.
- the third components which are also selected from anti-ultraviolet agents, antifungal agents, fragrances, etc., such as ferrous lsalicylate and 2,4 dihydroxybenzophenone to the dispersion medium in advance. Good.
- the first liquid and Z or the second liquid may be applied as long as the finished surface has a uniform wrinkle.
- spray coating, towel, sponge examples thereof include a method of applying with a means such as a nonwoven fabric and a tissue, and brushing.
- the second liquid may be applied onto the black film formed thereby.
- the first liquid is dispersed. Volatilize the medium and It is more preferable to dry the formed black film and then apply the second liquid onto the black film.
- the dispersion medium of the second liquid is volatilized, and the coating film formed thereby is dried. Then, excess components on the coating film are removed from scratches such as towels, non-woven fabric, and fleece. It may be finished by wiping with something difficult to attach.
- Each 1st liquid of prescription examples 1-4 was prepared in each ratio shown in Table 1, respectively.
- Acrylic ester polymer L-53P 15 made by Kyoyo Chemical Co., Ltd.
- Silicone resin KF 9021 15 made by Shin-Etsu Chemical Co., Ltd.
- the first liquid formulation example 1 prepared above is applied to about one third of the side surface of one tire, and further, the second liquid Formulation Example 1 was applied (Example 1).
- a second liquid formulation example 2 prepared above is applied to another portion of about one third of the side surface of the same tire of the same passenger car. (Example 2).
- the first liquid formulation example 3 prepared above is applied to another one third of the side surface of the same tire of the same passenger car, and the second liquid formulation example 1 is further applied thereon. Was applied (Example 3).
- the first liquid formulation example 4 prepared above is applied to about one third of the side surface of another tire of the same passenger car, and the second liquid formulation example 1 is further applied thereon. Applied (Example 4).
- the first liquid formulation example 1 prepared above is applied to another one third of the side surface of the same tire of the same passenger car, and the second liquid formulation example 2 is further applied thereto.
- the first liquid formulation example 1 prepared above is applied to another one third of the side surface of the same tire of the same passenger car, and the second liquid formulation example 3 is further applied thereto.
- the first liquid formulation example 1 prepared above is applied to about one third of the side surface of another tire of the same passenger car, and the second liquid formulation example 4 is further applied thereon. Applied (Example 7).
- the first liquid formulation example 1 prepared above is applied to another one third of the side surface of the same tire of the same passenger car, and the second liquid comparative formulation example is further applied thereon. (Comparative example
- the first liquid formulation example 1 prepared above is applied to about one third of the side surface of another tire of the same passenger car, and further, the second liquid comparative formulation example 7 is applied thereon. (Comparative Example 3).
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Paints Or Removers (AREA)
- Tires In General (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004273236A JP2007332165A (ja) | 2004-09-21 | 2004-09-21 | タイヤコーティング剤セット及びタイヤコーティング方法 |
JP2004-273236 | 2004-09-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006033208A1 true WO2006033208A1 (ja) | 2006-03-30 |
Family
ID=36089972
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/014935 WO2006033208A1 (ja) | 2004-09-21 | 2005-08-16 | タイヤコーティング剤セット及びタイヤコーティング方法 |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP2007332165A (ja) |
TW (1) | TW200610794A (ja) |
WO (1) | WO2006033208A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008308662A (ja) * | 2007-05-11 | 2008-12-25 | Canon Inc | 水性インク、インクセット、画像形成方法、及び画像形成装置 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014203852A1 (ja) * | 2013-06-20 | 2014-12-24 | 株式会社Dnpファインケミカル | 加飾タイヤ及びその製造方法 |
KR101731072B1 (ko) * | 2014-03-14 | 2017-04-28 | 주식회사 불스원 | 타이어 코팅용 조성물 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01207369A (ja) * | 1988-02-16 | 1989-08-21 | Nippon Yuka Kogyo Kk | タイヤ用艶出し剤組成物 |
JPH02194001A (ja) * | 1989-01-20 | 1990-07-31 | Shin Etsu Chem Co Ltd | ワックス組成物及びその製造方法 |
JPH08239629A (ja) * | 1995-03-06 | 1996-09-17 | Sofuto Kyukyu Corp:Kk | タイヤ用艶だし剤組成物 |
JP2000073013A (ja) * | 1998-06-19 | 2000-03-07 | Kansai Paint Co Ltd | 艶出し剤 |
JP2002256225A (ja) * | 2001-03-01 | 2002-09-11 | Wilson:Kk | タイヤ及びホイール用保護艶出し剤 |
-
2004
- 2004-09-21 JP JP2004273236A patent/JP2007332165A/ja not_active Withdrawn
-
2005
- 2005-07-26 TW TW094125317A patent/TW200610794A/zh unknown
- 2005-08-16 WO PCT/JP2005/014935 patent/WO2006033208A1/ja active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01207369A (ja) * | 1988-02-16 | 1989-08-21 | Nippon Yuka Kogyo Kk | タイヤ用艶出し剤組成物 |
JPH02194001A (ja) * | 1989-01-20 | 1990-07-31 | Shin Etsu Chem Co Ltd | ワックス組成物及びその製造方法 |
JPH08239629A (ja) * | 1995-03-06 | 1996-09-17 | Sofuto Kyukyu Corp:Kk | タイヤ用艶だし剤組成物 |
JP2000073013A (ja) * | 1998-06-19 | 2000-03-07 | Kansai Paint Co Ltd | 艶出し剤 |
JP2002256225A (ja) * | 2001-03-01 | 2002-09-11 | Wilson:Kk | タイヤ及びホイール用保護艶出し剤 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008308662A (ja) * | 2007-05-11 | 2008-12-25 | Canon Inc | 水性インク、インクセット、画像形成方法、及び画像形成装置 |
Also Published As
Publication number | Publication date |
---|---|
TW200610794A (en) | 2006-04-01 |
JP2007332165A (ja) | 2007-12-27 |
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