JP4516061B2 - ポリベンゾイミダゾール塗料組成物 - Google Patents
ポリベンゾイミダゾール塗料組成物 Download PDFInfo
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- JP4516061B2 JP4516061B2 JP2006356553A JP2006356553A JP4516061B2 JP 4516061 B2 JP4516061 B2 JP 4516061B2 JP 2006356553 A JP2006356553 A JP 2006356553A JP 2006356553 A JP2006356553 A JP 2006356553A JP 4516061 B2 JP4516061 B2 JP 4516061B2
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- Prior art keywords
- polybenzimidazole
- coating composition
- solvent
- coating
- mixed solvent
- Prior art date
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- 229920002480 polybenzimidazole Polymers 0.000 title claims description 74
- 239000004693 Polybenzimidazole Substances 0.000 title claims description 72
- 239000008199 coating composition Substances 0.000 title claims description 35
- 238000000576 coating method Methods 0.000 claims description 38
- 239000011248 coating agent Substances 0.000 claims description 35
- 239000002245 particle Substances 0.000 claims description 33
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 24
- 239000012046 mixed solvent Substances 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 239000002798 polar solvent Substances 0.000 claims description 19
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- 239000006184 cosolvent Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 6
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 239000002904 solvent Substances 0.000 description 14
- 239000000758 substrate Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 125000005647 linker group Chemical group 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000000889 atomisation Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000007824 aliphatic compounds Chemical class 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 150000001787 chalcogens Chemical group 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- -1 for example Substances 0.000 description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 1
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
- RQOKAVXYXISUJQ-UHFFFAOYSA-N 1h-benzimidazole;methane Chemical compound C.C1=CC=C2NC=NC2=C1 RQOKAVXYXISUJQ-UHFFFAOYSA-N 0.000 description 1
- KBNWXLAYHMRRGH-UHFFFAOYSA-N 1h-benzimidazole;propane Chemical compound CCC.C1=CC=C2NC=NC2=C1 KBNWXLAYHMRRGH-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- CRWNQZTZTZWPOF-UHFFFAOYSA-N 2-methyl-4-phenylpyridine Chemical compound C1=NC(C)=CC(C=2C=CC=CC=2)=C1 CRWNQZTZTZWPOF-UHFFFAOYSA-N 0.000 description 1
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001334 alicyclic compounds Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052798 chalcogen Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007766 curtain coating Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 125000005550 pyrazinylene group Chemical group 0.000 description 1
- 125000005551 pyridylene group Chemical group 0.000 description 1
- 238000000790 scattering method Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000005730 thiophenylene group Chemical group 0.000 description 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
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
- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
- C09D179/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/65—Additives macromolecular
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paints Or Removers (AREA)
Description
なお、水以外に同様の分散安定性と溶剤浸透性の補助作用を有する溶媒であれば、水の代わりに用いることもできるが、そのような溶媒は非常に特殊であり、入手容易性あるいはコストの点から不利である。
平均粒子径13μmのポリベンゾイミダゾール(AZエレクトロニックマテリアルズ株式会社)を54g、水を54g、ブチルセロソルブ18g、ジメチルスルホキシド(以下DMSO)20g、N−メチルピロリドン(以下NMP)54gを500ml容器に入れ撹拌機で良く撹拌して均一分散させ、ポリベンゾイミダゾールの含有量が27重量%の塗料組成物を得た。この塗料組成物を、溶剤脱脂処理のみをしたA5052アルミ基材(100mm×50mm×1mm)に常温でノズル径0.8φで0.2MPaの圧力でスプレー塗装し、80〜100℃で乾燥溶解させた後、150℃まで昇温し2〜3時間保持後200℃まで昇温し1時間保持、250℃まで昇温し3時間保持、300℃で1時間、350℃で1時間焼成して、厚さ22μmの塗膜を得た。
この工程での塗装性、塗膜の平滑性、塗膜密着性および10日後の塗料組成物の安定性を調べた。得られた結果は表1に示す通りであった。
溶媒組成およびポリベンゾイミダゾール粒子の平均粒子径を表1に示したとおりに変更したほかは実施例1と同様に評価した。得られた結果は表1に示す通りであった。
表1に示される水を含まない混合溶媒を用いたほかは実施例1と同様に評価した。得られた結果は表1に示す通りであった。
特許文献1の実施例1の記載に準じて、ポリベンゾイミダゾールの含有量が10重量%の塗料組成物を調製し、実施例1と同様に評価した。得られた結果は表1に示す通りであった。
ポリベンゾイミダゾールの含有量を27重量%とした他は、比較例4と同様にして塗料組成物を調製し、実施例1と同様に評価した。得られた結果は表1に示す通りであった。
Claims (6)
- 混合溶媒中に平均粒子径が0.5〜50μmのポリベンゾイミダゾール粒子が分散されており、
前記混合溶媒が、水と、20℃におけるポリベンゾイミダゾールの溶解度が1g/l以上の極性溶媒と、アルコール、エーテル、およびケトンからなる群から選ばれる少なくとも1種の共溶媒とを含んでなり、
前記極性溶媒がN,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、ジメチルスルホキシド、およびN−メチルピロリドンからなる群から選択される少なくとも2種類であり、
該混合溶媒全体に対して、前記水が5〜75重量%、前記共溶媒が50重量%以下含有することを特徴とするポリベンゾイミダゾール塗料組成物。 - 前記極性溶媒がジメチルスルホオキシドとN−メチルピロリドンとの混合溶媒であることを特徴とする請求項1に記載のポリベンゾイミダゾール塗料組成物。
- 前記極性溶媒がジメチルスルホオキシドとN−メチルピロリドンとN,N−ジメチルアセトアミドとの混合溶媒であることを特徴とする請求項1に記載のポリベンゾイミダゾール塗料組成物。
- ポリベンゾイミダソールの含有量が10〜60重量%である特許請求項1〜3のいずれか1項に記載のポリベンゾイミダゾール塗料組成物。
- 前記ポリベンゾイミダゾール塗料組成物は、スプレー塗布用であることを特徴とする特許請求項1〜4のいずれか1項に記載のポリベンゾイミダゾール塗料組成物。
- 基材上に、請求項1〜5のいずれか1項に記載のポリベンゾイミダゾール塗料組成物を塗布し、
形成された塗膜を60〜120℃で加熱する工程を含んでなることを特徴とする、ポリベンゾイミダゾール被膜の形成方法。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006356553A JP4516061B2 (ja) | 2006-12-28 | 2006-12-28 | ポリベンゾイミダゾール塗料組成物 |
PCT/JP2007/074801 WO2008081770A1 (ja) | 2006-12-28 | 2007-12-25 | ポリベンゾイミダゾール塗料組成物 |
US12/448,500 US20100028547A1 (en) | 2006-12-28 | 2007-12-25 | Polybenzimidazole coating composition |
EP07860030A EP2123725A1 (en) | 2006-12-28 | 2007-12-25 | Polybenzoimidazole coating composition |
TW096150498A TW200844193A (en) | 2006-12-28 | 2007-12-27 | Polybenzoimidazole coating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006356553A JP4516061B2 (ja) | 2006-12-28 | 2006-12-28 | ポリベンゾイミダゾール塗料組成物 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2008163261A JP2008163261A (ja) | 2008-07-17 |
JP2008163261A5 JP2008163261A5 (ja) | 2010-02-12 |
JP4516061B2 true JP4516061B2 (ja) | 2010-08-04 |
Family
ID=39588453
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006356553A Active JP4516061B2 (ja) | 2006-12-28 | 2006-12-28 | ポリベンゾイミダゾール塗料組成物 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20100028547A1 (ja) |
EP (1) | EP2123725A1 (ja) |
JP (1) | JP4516061B2 (ja) |
TW (1) | TW200844193A (ja) |
WO (1) | WO2008081770A1 (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8475925B2 (en) * | 2010-06-22 | 2013-07-02 | Pbi Performance Products, Inc. | PBI/epoxy coatings |
CN103102796B (zh) * | 2013-01-10 | 2015-05-13 | 东华大学 | 一种苯并咪唑型聚酰亚胺漆包线漆及其制备方法 |
US9920358B2 (en) | 2013-06-27 | 2018-03-20 | New England Biolabs, Inc. | Helicase suppression of non-template amplification |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4813701B1 (ja) * | 1970-08-25 | 1973-04-28 | ||
JPS63286475A (ja) * | 1987-05-20 | 1988-11-24 | Kansai Paint Co Ltd | 被覆用組成物 |
JPH05339401A (ja) * | 1992-06-09 | 1993-12-21 | Hoechst Japan Ltd | ポリベンズイミダゾール被膜の形成方法 |
JPH08131949A (ja) * | 1994-11-15 | 1996-05-28 | Hoechst Japan Ltd | ポリベンゾイミダゾール被膜の形成方法 |
JPH08157772A (ja) * | 1994-12-08 | 1996-06-18 | Toyo Seikan Kaisha Ltd | 水性塗料及びそれを用いる塗装方法 |
JP2002346432A (ja) * | 2001-05-23 | 2002-12-03 | Clariant (Japan) Kk | 樹脂粒子の分級方法 |
WO2003006565A1 (fr) * | 2001-06-15 | 2003-01-23 | Daikin Industries, Ltd. | Composition de revetement de fluororesine, film de revetement et objet revetu |
JP2006096971A (ja) * | 2004-08-31 | 2006-04-13 | Sanyo Chem Ind Ltd | 中空樹脂粒子の製造方法 |
JP2006307166A (ja) * | 2005-03-31 | 2006-11-09 | Dainippon Printing Co Ltd | 高分子化合物前駆体、高透明性ポリイミド前駆体、高分子化合物、これらを用いた樹脂組成物及び物品 |
JP2007269936A (ja) * | 2006-03-31 | 2007-10-18 | Sumikou Junkatsuzai Kk | 乾性潤滑被膜組成物 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3389122A (en) * | 1966-05-18 | 1968-06-18 | Ashland Oil Inc | Novel polyamides and heterocyclic polymers prepared from aromatic hydrazides and dicarboxylic acid dichlorides |
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2006
- 2006-12-28 JP JP2006356553A patent/JP4516061B2/ja active Active
-
2007
- 2007-12-25 EP EP07860030A patent/EP2123725A1/en not_active Withdrawn
- 2007-12-25 WO PCT/JP2007/074801 patent/WO2008081770A1/ja active Application Filing
- 2007-12-25 US US12/448,500 patent/US20100028547A1/en not_active Abandoned
- 2007-12-27 TW TW096150498A patent/TW200844193A/zh unknown
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4813701B1 (ja) * | 1970-08-25 | 1973-04-28 | ||
JPS63286475A (ja) * | 1987-05-20 | 1988-11-24 | Kansai Paint Co Ltd | 被覆用組成物 |
JPH05339401A (ja) * | 1992-06-09 | 1993-12-21 | Hoechst Japan Ltd | ポリベンズイミダゾール被膜の形成方法 |
JPH08131949A (ja) * | 1994-11-15 | 1996-05-28 | Hoechst Japan Ltd | ポリベンゾイミダゾール被膜の形成方法 |
JPH08157772A (ja) * | 1994-12-08 | 1996-06-18 | Toyo Seikan Kaisha Ltd | 水性塗料及びそれを用いる塗装方法 |
JP2002346432A (ja) * | 2001-05-23 | 2002-12-03 | Clariant (Japan) Kk | 樹脂粒子の分級方法 |
WO2003006565A1 (fr) * | 2001-06-15 | 2003-01-23 | Daikin Industries, Ltd. | Composition de revetement de fluororesine, film de revetement et objet revetu |
JP2006096971A (ja) * | 2004-08-31 | 2006-04-13 | Sanyo Chem Ind Ltd | 中空樹脂粒子の製造方法 |
JP2006307166A (ja) * | 2005-03-31 | 2006-11-09 | Dainippon Printing Co Ltd | 高分子化合物前駆体、高透明性ポリイミド前駆体、高分子化合物、これらを用いた樹脂組成物及び物品 |
JP2007269936A (ja) * | 2006-03-31 | 2007-10-18 | Sumikou Junkatsuzai Kk | 乾性潤滑被膜組成物 |
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TW200844193A (en) | 2008-11-16 |
EP2123725A1 (en) | 2009-11-25 |
US20100028547A1 (en) | 2010-02-04 |
JP2008163261A (ja) | 2008-07-17 |
WO2008081770A1 (ja) | 2008-07-10 |
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