WO2006013713A1 - 塗装材剥離剤及び塗装材剥離シート - Google Patents
塗装材剥離剤及び塗装材剥離シート Download PDFInfo
- Publication number
- WO2006013713A1 WO2006013713A1 PCT/JP2005/013108 JP2005013108W WO2006013713A1 WO 2006013713 A1 WO2006013713 A1 WO 2006013713A1 JP 2005013108 W JP2005013108 W JP 2005013108W WO 2006013713 A1 WO2006013713 A1 WO 2006013713A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- coating material
- sheet
- agent
- release agent
- material release
- Prior art date
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
- C09D9/00—Chemical paint or ink removers
- C09D9/005—Chemical paint or ink removers containing organic solvents
Definitions
- the present invention relates to a detached house, an apartment house, a factory, and the like, outer walls, inner walls, roofs, floors, flooring, wood furniture, joinery, crafts, musical instruments, wood, fishing boats, passenger ships, cargo ships, pleasure ports
- coating materials used for finishing materials such as ships, aircraft, trains, automobiles, vehicles such as passes, industrial products such as industrial machinery, or equipment such as bridges, signs, playground equipment, etc.
- Suitable for coating material release agent and coating material release sheet are suitable for coating material release agent and coating material release sheet.
- a stripping agent When stripping the coating material, it is common practice to apply a stripping agent on the coating material from the viewpoint of shortening the stripping time.
- a release agent mainly composed of methylene chloride or the like is generally used.
- chlorinated solvents such as methylene chloride may cause environmental pollution such as the generation of dioxin during combustion and have excellent release properties, but their use may be limited in the future. There is.
- JP-A Nos. 10-2 7 9 8 50 JP-A Nos. 10 3 3 1 4 3 5 and JP-A 2 00 0-1 6 3 7
- it was difficult to uniformly apply the release agent it was difficult to uniformly apply the release agent, and as a result, there was a problem in that the peeled state varied.
- the object of the present invention is to plasticize and soften coating materials such as buildings, timber, ships, vehicles, industrial products, equipment, etc. without melting them, facilitating the peeling work of the coating materials, and the environment. It is to provide a coating material stripping agent and a coating material stripping sheet that have less adverse effects on the skin. Disclosure of the invention
- the coating material release agent of the present invention is a coating material release agent comprising a composition substantially free of a halogen-based compound, and the composition has a boiling point of 1 13 ° C 2300 ° C.
- the base material is impregnated with the coating material release agent.
- the sheet base material is a composite base material composed of a fiber assembly such as a nonwoven fabric and an organic film base material.
- the coating material release sheet has a configuration in which two surfaces of the composite base material impregnated with the coating material release agent are overlapped.
- the sheet base material is impregnated with the coating material release agent from 100 to 200 g Zm2.
- a non-halogen high boiling point organic solvent, a soluble organic polymer compound, and a thixotropic agent as a main component are substantially halogenated. It has been found that a composition containing no compound may be used as a coating material remover. In this case, it was also found that a surfactant, a colorant, a filler and the like may be added as necessary.
- the above-mentioned coating material release agent may be used as a coating material peeling sheet in which a sheet substrate is impregnated.
- a coating material peeling sheet in which a sheet substrate is impregnated.
- a composite substrate of a fiber assembly such as a nonwoven fabric and an organic film was used as the sheet base material, and the surface of the fiber assembly such as a nonwoven fabric of the sheet base material was impregnated with a coating material release agent. It has been found that it can be used as a coating material peeling sheet.
- the above coating material release sheet can be laminated with a separator on the non-woven fabric surface before use. If the surfaces impregnated with the release agent are stacked, there will be no generation of dust during use, and there is no separator on the nonwoven fabric surface of the paint release sheet. It was very convenient without being taken.
- the coating material remover of the present invention when used for peeling coating materials such as buildings, wood, ships, vehicles, industrial products, equipment, etc., apply the coating material remover of the present invention to the coating material to be peeled, or
- the surface of the coating material release sheet impregnated with the coating material release agent is affixed to the coating material to be peeled, and the coating material is softened and plasticized so that the coating material can be easily peeled off from the ground using a spatula be able to.
- the coating material peeling sheet it is natural that there is no uneven coating of the coating material remover, and there is almost no volatilization of the coating material remover.
- the coating material can be peeled stably, the work time required for peeling can be shortened, and difficult skill level is not required.
- an organic solvent having a boiling point in the range of 1 13 ° C. to 2 30 ° C. is desirable. More preferably, an organic solvent having a boiling point in the range of 1556 ° C to 230 ° C is desirable. If the boiling point is less than 1 13 ° C, the solvent is likely to volatilize, making it difficult to remove the coating material. If the boiling point exceeds 2 30 ° C, the penetrating power to the coating material will be reduced, and the peeling performance will be reduced. Inferior.
- Non-halogen high boiling point organic solvents include, for example, alcoholic organic solvents such as methyl caffeine solve, ptylcetic solve, and propargyl alcohol, and ester acetates such as methylcecsolve solvate, ethyl solvate solvate, and ptylcetal solvate.
- alcoholic organic solvents such as methyl caffeine solve, ptylcetic solve, and propargyl alcohol
- ester acetates such as methylcecsolve solvate, ethyl solvate solvate, and ptylcetal solvate.
- Organic solvent diethylene glycol monoethyl ether (carbitol), diethylene glycol monomethyl ether, diethylene glycol Mono-n-butyl ether (butyl carbitol), diethylene glycol dimethyl ether, diethylene glycol mono-letyl ether, jet ethylene glycol mono-resin n-butyl ether, diethylene glycol monoethyl ether acetate (carbitol acetate), diethylene glycol mono n-butyl ether acetate Glycol ethers such as dito, cyclohexanone, N-methyl-2-pyrrolidinone, methyl pyruvate, ethyl pyruvate, and N, N-dimethylacetamide. These non-halogen high boiling point organic solvents are used alone or in combination of two or more. >
- the non-halogen high boiling point organic solvent to be used needs not only high peelability, but also low odor and high safety. Furthermore, in order to increase the viscosity of the coating material release agent and at the same time improve the adhesion to the coating material when the coating material release sheet is bonded to the coating material and the retention of the coating material release sheet, Use molecular compounds.
- the soluble organic polymer compound used in the present invention is preferably a soluble organic polymer compound having a weight average molecular weight in the range of 10,000 to 1,000,000.
- the blending amount is 1 to 50 parts by weight with respect to 100 parts by weight of the solution comprising the non-halogen high boiling point organic solvent and the soluble organic polymer compound. Is preferred. More preferably, it is 1 to 30 parts by weight.
- the amount of the soluble organic polymer compound is less than 1 part by weight, the retentivity of the coating material release agent is reduced, and when it is more than 50 parts by weight, the coating material release agent is particularly too viscous. Therefore, either case is not practically preferable.
- the soluble organic polymer compounds are used alone or in combination of two or more.
- a thixotropic agent is used to increase the retention of the coating material release agent when the coating material release agent is applied to the coating material, and the retention of the sheet when the coating material release sheet is bonded to the coating material.
- the thixotropic agent used in the present invention include fine or ultrafine organic or inorganic compounds, for example, trade names such as Aerosil 200, Aerosil 300, and Aerosil 320. Examples thereof include silicon-based ultrafine powder.
- the blending amount is preferably 1 to 15 parts by weight with respect to 100 parts by weight of the solution comprising the non-halogen high boiling point organic solvent and the soluble organic polymer compound.
- the thixotropic agent When the thixotropic agent is less than 1 part by weight, the retention of the coating material release agent is reduced, and when it is more than 15 parts by weight, the coating material release agent is difficult to impregnate the composite substrate. Therefore, either case is not practically preferable. Furthermore, if necessary, nonionic, anionic or cationic surfactants, colorants, and other fillers may be added.
- the base material used for the coating material release sheet is preferably a base material that can be impregnated with the coating material release agent and that can suppress the volatilization of the coating material release agent and can be stably maintained.
- a composite substrate of an organic film and a fiber assembly such as nonwoven fabric, felt, napped knitted fabric, and raised knitted fabric.
- the basis weight of the fiber assembly is not particularly limited as long as the required amount of coating material release agent can be soaked and retained, but in particular, the basis weight is preferably 20 to 200 g Zm 2 . Further, a sheet made of sponge or the like may be used instead of the above fiber assembly.
- the amount of the coating material peeling agent impregnated in the substrate varies depending on the type of coating Paneling to be cane peeling usually be immersed containing desirable in the range of 1 00 ⁇ 2000 gZm 2. If the amount of paint release agent is less than 100 gZm 2 , the release performance may be insufficient. If it is more than 2000 g / m 2, from the viewpoint of retention of the paint release agent It is not preferable for practical use.
- 100 g / m 2 is impregnated on the nonwoven fabric surface composed of a composite base material of a nonwoven fabric having a basis weight of 20 g / m 2 and a polyester film having a thickness of 1 2 ⁇ 111.
- a release sheet was obtained.
- the nonwoven fabric portion of the sheet base material was appropriately impregnated with the coating material release agent.
- the product form is a configuration in which two non-woven fabric surfaces impregnated with a coating material release agent are overlapped. This makes it possible to use the entire amount of the coating material remover impregnated, which is extremely favorable.
- various coating materials were peeled off.
- the nonwoven fabric surface of the sheet base material impregnated with the coating material release agent was pressed against the coating material surface for pasting.
- Paste paint stripping sheet The sample for the paint coating peeling test was left standing vertically, but it was confirmed that the coating material peeling sheet did not shift and had sufficient retention. Then, after leaving for a certain period of time, the coating material release sheet was removed, and the coating material was peeled off with a spatula. .
- the coating material release agent was impregnated with 2000 gZm 2 on a nonwoven fabric surface composed of a composite base material of a nonwoven fabric having a basis weight of 200 gZm 2 and a polyester film having a thickness of 12 im.
- a coating material release sheet was obtained.
- the nonwoven fabric portion of the sheet base material was appropriately impregnated with the coating material release agent.
- the product form is a configuration in which two non-woven fabric surfaces impregnated with a coating material release agent are overlapped. This makes it possible to use the entire amount of the coating material remover impregnated, which is very convenient.
- various coating materials were peeled off in the same manner as in Example 1.
- the above-mentioned coating material release agent was impregnated with 800 g Zm 2 on a non-woven fabric surface composed of a composite base material of a nonwoven fabric having a basis weight of 100 g / m 2 and a polyester film having a thickness of 12 ⁇ m.
- a paint release sheet was obtained.
- the nonwoven fabric portion of the sheet base material was appropriately impregnated with the coating material peeling agent.
- the product form is a configuration in which two non-woven fabric surfaces impregnated with a coating material release agent are overlapped. This makes it possible to use the entire amount of the coating material remover impregnated, which is extremely convenient.
- Example 4 Using the coating material release sheet thus prepared, various coating materials were peeled off in the same manner as in Example 1. Although the sample for the coating material peeling test with the coating material peeling sheet attached was left standing vertically, the coating material peeling sheet was not displaced and it was confirmed that there was sufficient retention. After that, after leaving for a certain period of time, the coating material release sheet was removed, and the coating material was peeled off with a spatula. However, although there is a difference in the time until it can be peeled off, all the coating materials are clean as in Example 1. It was possible to peel off. (Specific example 4)
- a release sheet was obtained.
- this coating material release sheet the nonwoven fabric portion of the sheet base material was appropriately impregnated with the coating material release agent.
- the product form is a configuration in which two non-woven fabric surfaces impregnated with a coating material release agent are overlapped. This makes it possible to use the entire amount of the coating material stripping agent impregnated, which is extremely convenient.
- various coating materials were separated in the same manner as in Example 1. Although the sample for the coating material peeling test with the coating material peeling sheet attached was left standing vertically, it was confirmed that the coating material peeling sheet did not shift and had sufficient retention.
- Example 1 After that, after leaving for a certain period of time, the coating material release sheet was removed, and the coating material was peeled off with a spatula. However, although there is a difference in the time until it can be peeled off, all the coating materials are clean as in Example 1. It was possible to peel off.
- the coating material release agent described above is applied to a nonwoven fabric with a basis weight of 80 gZm 2 and a thickness of 1 2 ⁇ ⁇ .
- a nonwoven fabric surface composed of a composite base material with a polyester film was impregnated with 500 g / m 2 to obtain a coating material release sheet.
- this coating material release sheet the nonwoven fabric portion of the sheet base material was appropriately impregnated with the coating material release agent.
- the product form is a configuration in which two non-woven fabric surfaces impregnated with a coating material release agent are overlapped. This makes it possible to use the entire amount of the coating material remover impregnated, which is very convenient.
- various coating materials were peeled off in the same manner as in Example 1.
- the sample for the coating material peeling test with the coating material peeling sheet attached was left standing vertically, but it was confirmed that the coating material peeling sheet did not shift and had sufficient retention. After that, after leaving for a certain period of time, the coating material release sheet was removed, and the coating material was peeled off with a spatula. However, although there is a difference in the time until it can be peeled off, as with Example 1, all coating materials are clean. It was possible to peel off.
- N-methyl-2-pyrrolidinone (boiling point 20 2 ° C) 60 parts, carbitol acetate (boiling point 2 18 ° C) 20 parts, polyester resin with a weight average molecular weight of about 20,000 (Toyobo's Byron RV — 1 0 3) 2 0 parts, 6 parts ultrafine silicon dioxide (Aerosil 3 0 0) are mixed well, and the viscosity is about 2500 m Pa ⁇ s (measurement conditions: 5 rotations, 25 ° C The paste-like coating material remover was obtained.
- the coating material release agent described above was impregnated with 200 g / m 2 on a nonwoven fabric surface composed of a composite substrate of a nonwoven fabric having a basis weight of 50 g Zm 2 and a polyester film having a thickness of 12 A release sheet was obtained.
- this coating material release sheet the nonwoven fabric portion of the sheet base material was appropriately impregnated with the coating material release agent.
- the product form is a structure in which two non-woven fabric surfaces impregnated with a coating material release agent are overlapped. This makes it possible to use the entire amount of the coating material remover impregnated, which is very convenient.
- various coating materials were peeled off in the same manner as in Example 1.
- the coating material release agent and the coating material release sheet of the present invention showed excellent peelability and excellent workability.
- this coating material release sheet was used for a coating material peeling test with a coating material release sheet attached. When the sample was placed upright and left for 24 hours, it was found that the coating material release sheet was displaced and the sheet retention was insufficient.
- a coating material release sheet was obtained with the same composition and configuration as in Example 3 except that the coating amount of the coating material release agent was 2500 g / m 2 .
- the nonwoven fabric part of the sheet base material was appropriately impregnated with the coating material release agent.
- a sample for coating material peeling test with a coating material release sheet attached was used. After standing for 24 hours in a vertical position, it was found that the coating material peeling sheet shifted and the sheet retention was insufficient.
- a coating material release sheet was obtained in the same composition and configuration as in Example 1 except that the soluble organic polymer compound was not used.
- this coating material release sheet the nonwoven fabric portion of the sheet base material was not appropriately impregnated with the coating material release agent. Also, as in Example 1, for paint material peel test with paint material release sheet attached When this sample was stood vertically for 24 hours, it was found that the coating material peeling sheet was displaced and the sheet retention was insufficient.
- a paint release sheet was obtained with the same composition and configuration as in Example 2 except that the thixotropic agent was not used.
- the non-woven fabric part of the sheet base material was appropriately impregnated with the coating material release agent, but in the same manner as in Example 2, the sample for the coating material peeling test with the coating material release sheet attached was used. Standing vertically for 24 hours, it was found that the paint release sheet was displaced and the sheet retention was insufficient.
- a coating material release sheet was obtained with the same composition and configuration as in Example 3 except that the amount of the soluble organic polymer material was 60 parts.
- This coating material peeling sheet is difficult for the coating material stripping agent to be included in the nonwoven fabric part of the sheet base material, and in the same manner as in Example 3, it is used for the coating material peeling test. When the sample was stood vertically for 24 hours, it was found that the permeability of the paint stripper was insufficient.
- a coating material release sheet was obtained in the same composition and configuration as in Example 4 except that the amount of the thixotropic pea agent was 20 parts.
- the nonwoven fabric portion of the sheet base material was not appropriately impregnated with the coating material release agent.
- the coating material peeling test sample with the coating material peeling sheet attached was placed upright and left for 24 hours, the coating material peeling sheet shifted and the sheet retention was insufficient. It turns out that. It was also found that the coating material stripper has insufficient permeability.
- Example 5 and A coating material release sheet was obtained with the same composition and configuration.
- the non-woven fabric portion of the sheet base material was appropriately impregnated with the coating material release agent.
- the coating material release sheet was used for a coating material peeling test. The coating material stripper was volatilized after standing for 24 hours in a vertical position. It was also found that the coating material release sheet was displaced and the sheet retention was insufficient.
- the present invention includes a non-halogen high boiling point organic solvent having a boiling point of 1 13 to 2300 ° C. and a soluble organic polymer compound having a weight average molecular weight of 10,000 to 100000. And a composition containing essentially a thixotropic agent and containing no halogen compound as a coating material release agent, and the coating material release agent comprises a fiber assembly such as a nonwoven fabric and an organic film substrate. Since the coating material peeling sheet impregnated into the sheet base material is used, by implementing the present invention, the coating material has excellent softening properties, is safe, and is environmentally friendly. It is also possible to provide an excellent coating material release agent and a coating material release sheet.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006531360A JP5226213B2 (ja) | 2004-07-14 | 2005-07-08 | 塗装材剥離剤及び塗装材剥離シート |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004-206953 | 2004-07-14 | ||
JP2004206953 | 2004-07-14 |
Publications (1)
Publication Number | Publication Date |
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WO2006013713A1 true WO2006013713A1 (ja) | 2006-02-09 |
Family
ID=35787006
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/013108 WO2006013713A1 (ja) | 2004-07-14 | 2005-07-08 | 塗装材剥離剤及び塗装材剥離シート |
Country Status (3)
Country | Link |
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JP (1) | JP5226213B2 (ja) |
TW (1) | TW200606229A (ja) |
WO (1) | WO2006013713A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010131539A1 (ja) * | 2009-05-13 | 2010-11-18 | 国立大学法人岡山大学 | 塗膜除去剤及びそれを用いた塗膜除去方法 |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5920400A (ja) * | 1982-07-27 | 1984-02-02 | 滝口 好 | 洗浄剤 |
JPH06501284A (ja) * | 1990-10-01 | 1994-02-10 | ヴェロナ インコーポレイテッド | N―メチル―2―ピロリドン(NMP)および/またはγ―ブチロラクトン(BLO)ニスおよび塗料除去溶媒を活性化させる方法 |
JPH10279850A (ja) * | 1997-04-04 | 1998-10-20 | Yamaichi Kagaku Kogyo Kk | 壁面等の塗膜剥離剤及びその剥離方法 |
JPH11513724A (ja) * | 1995-10-18 | 1999-11-24 | エルフ アトケム ソシエテ アノニム | ペイント剥離用濃縮組成物 |
JP2000001637A (ja) * | 1998-06-15 | 2000-01-07 | Yamaichi Kagaku Kogyo Kk | 外壁等の塗膜並びにプラスティックタイル用剥離剤及び剥離方法 |
JP2000017289A (ja) * | 1998-07-01 | 2000-01-18 | Car Mate Mfg Co Ltd | ガラス質被膜の剥離用組成物および剥離方法 |
JP2000290543A (ja) * | 1999-03-25 | 2000-10-17 | Atofina | 特に建築工業で使用可能な剥離用組成物 |
JP2002030234A (ja) * | 2000-05-26 | 2002-01-31 | Atofina | 建築および船舶分野で使用可能な剥離組成物 |
-
2005
- 2005-07-08 WO PCT/JP2005/013108 patent/WO2006013713A1/ja active Application Filing
- 2005-07-08 JP JP2006531360A patent/JP5226213B2/ja not_active Expired - Fee Related
- 2005-07-11 TW TW094123443A patent/TW200606229A/zh not_active IP Right Cessation
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5920400A (ja) * | 1982-07-27 | 1984-02-02 | 滝口 好 | 洗浄剤 |
JPH06501284A (ja) * | 1990-10-01 | 1994-02-10 | ヴェロナ インコーポレイテッド | N―メチル―2―ピロリドン(NMP)および/またはγ―ブチロラクトン(BLO)ニスおよび塗料除去溶媒を活性化させる方法 |
JPH11513724A (ja) * | 1995-10-18 | 1999-11-24 | エルフ アトケム ソシエテ アノニム | ペイント剥離用濃縮組成物 |
JPH10279850A (ja) * | 1997-04-04 | 1998-10-20 | Yamaichi Kagaku Kogyo Kk | 壁面等の塗膜剥離剤及びその剥離方法 |
JP2000001637A (ja) * | 1998-06-15 | 2000-01-07 | Yamaichi Kagaku Kogyo Kk | 外壁等の塗膜並びにプラスティックタイル用剥離剤及び剥離方法 |
JP2000017289A (ja) * | 1998-07-01 | 2000-01-18 | Car Mate Mfg Co Ltd | ガラス質被膜の剥離用組成物および剥離方法 |
JP2000290543A (ja) * | 1999-03-25 | 2000-10-17 | Atofina | 特に建築工業で使用可能な剥離用組成物 |
JP2002030234A (ja) * | 2000-05-26 | 2002-01-31 | Atofina | 建築および船舶分野で使用可能な剥離組成物 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010131539A1 (ja) * | 2009-05-13 | 2010-11-18 | 国立大学法人岡山大学 | 塗膜除去剤及びそれを用いた塗膜除去方法 |
JP2010285590A (ja) * | 2009-05-13 | 2010-12-24 | Okayama Univ | 塗膜除去剤及びそれを用いた塗膜除去方法 |
JP2010285592A (ja) * | 2009-05-13 | 2010-12-24 | Okayama Univ | 塗膜除去剤及びそれを用いた塗膜除去方法 |
Also Published As
Publication number | Publication date |
---|---|
JPWO2006013713A1 (ja) | 2008-05-01 |
TWI339675B (ja) | 2011-04-01 |
TW200606229A (en) | 2006-02-16 |
JP5226213B2 (ja) | 2013-07-03 |
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