JPH0788491B2 - Paint containing titanium oxide - Google Patents
Paint containing titanium oxideInfo
- Publication number
- JPH0788491B2 JPH0788491B2 JP62058252A JP5825287A JPH0788491B2 JP H0788491 B2 JPH0788491 B2 JP H0788491B2 JP 62058252 A JP62058252 A JP 62058252A JP 5825287 A JP5825287 A JP 5825287A JP H0788491 B2 JPH0788491 B2 JP H0788491B2
- Authority
- JP
- Japan
- Prior art keywords
- titanium oxide
- group
- coating
- resistance
- coating film
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims description 32
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 title claims description 32
- 239000003973 paint Substances 0.000 title description 7
- 238000000576 coating method Methods 0.000 claims description 34
- 239000011248 coating agent Substances 0.000 claims description 33
- 239000002245 particle Substances 0.000 claims description 18
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000011230 binding agent Substances 0.000 claims description 10
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052802 copper Inorganic materials 0.000 claims description 7
- 239000010419 fine particle Substances 0.000 claims description 7
- 229910052720 vanadium Inorganic materials 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 229910052745 lead Inorganic materials 0.000 claims description 6
- 229910052763 palladium Inorganic materials 0.000 claims description 6
- 229910052697 platinum Inorganic materials 0.000 claims description 6
- 229910052709 silver Inorganic materials 0.000 claims description 6
- 229910052721 tungsten Inorganic materials 0.000 claims description 6
- WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 claims description 3
- 229910052797 bismuth Inorganic materials 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000010408 film Substances 0.000 description 21
- 239000000126 substance Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 6
- 239000002131 composite material Substances 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 230000001699 photocatalysis Effects 0.000 description 5
- -1 silane compound Chemical class 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229910000077 silane Inorganic materials 0.000 description 4
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 230000005856 abnormality Effects 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 150000002736 metal compounds Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920005615 natural polymer Polymers 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 239000013522 chelant Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- OXYZDRAJMHGSMW-UHFFFAOYSA-N 3-chloropropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCl OXYZDRAJMHGSMW-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- LVACOMKKELLCHJ-UHFFFAOYSA-N 3-trimethoxysilylpropylurea Chemical compound CO[Si](OC)(OC)CCCNC(N)=O LVACOMKKELLCHJ-UHFFFAOYSA-N 0.000 description 1
- FPJPAIQDDFIEKJ-UHFFFAOYSA-N 4-trimethoxysilylbutanenitrile Chemical compound CO[Si](OC)(OC)CCCC#N FPJPAIQDDFIEKJ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- YUFXVINQLFINJU-UHFFFAOYSA-N acetic acid methyl 3-oxobutanoate Chemical compound C(CC(=O)C)(=O)OC.C(C)(=O)O YUFXVINQLFINJU-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001246 colloidal dispersion Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000001153 fluoro group Chemical class F* 0.000 description 1
- 150000003948 formamides Chemical class 0.000 description 1
- 230000005251 gamma ray Effects 0.000 description 1
- 150000002303 glucose derivatives Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- QBNKFXYJSJOGEL-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[O-2].[Ti+4].[Ti+4] QBNKFXYJSJOGEL-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
- 229920001308 poly(aminoacid) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- DHGFMVMDBNLMKT-UHFFFAOYSA-N propyl 3-oxobutanoate Chemical compound CCCOC(=O)CC(C)=O DHGFMVMDBNLMKT-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- YJDOIAGBSYPPCK-UHFFFAOYSA-N trimethoxy(3-morpholin-4-ylpropyl)silane Chemical compound CO[Si](OC)(OC)CCCN1CCOCC1 YJDOIAGBSYPPCK-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Surface Treatment Of Optical Elements (AREA)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、耐候性に優れた酸化チタン系塗料に関する。TECHNICAL FIELD The present invention relates to a titanium oxide-based coating material having excellent weather resistance.
本発明は、耐摩耗性,紫外線遮蔽,反射防止,反射増
加,耐薬品性を増すために有用な酸化チタンを含むコー
ティング塗料において、ビヒクル中に、有機基を含む特
定の金属化合物を含有させることにより、えられた塗膜
の酸化チタンに起因する光反応を抑え、塗膜の耐候性,
耐光性を改良したものである。The present invention relates to a coating paint containing titanium oxide, which is useful for increasing abrasion resistance, ultraviolet shielding, antireflection, increase in reflection, and chemical resistance, in which a specific metal compound containing an organic group is contained in a vehicle. Suppresses the photoreaction caused by titanium oxide in the obtained coating film, and improves the weather resistance of the coating film.
It has improved light resistance.
酸化チタンは、紫外線吸収能に優れ、また、微粒子を用
いた塗料は、赤外線の反射膜としても可能性が大きく、
種々の検討がなされている。Titanium oxide has an excellent ability to absorb ultraviolet rays, and a coating using fine particles has a great potential as an infrared reflective film.
Various studies have been made.
また、実用的には、白色顔料や紫外線遮蔽用の塗料混入
用として用いられている。In addition, it is practically used as a mixture of white pigments and ultraviolet shielding paint.
また、酸化チタンは光に対して活性であるが化学的に安
定である。この性質を透明な塗膜に応用することも検討
されている。この例としては、例えば、米国特許第4275
118号が挙げられる。Further, titanium oxide is chemically active although it is active with respect to light. Applying this property to a transparent coating film is also under study. Examples of this include, for example, U.S. Pat.
No. 118 is mentioned.
これらの例では、酸化チタンによる耐光性低下をおさえ
るために、酸化チタン粒子表面を光学的に安定な二酸化
ケイ素で被覆する、あるいは、シリコン系カップリング
剤およびコロイダルシリカをバインダとして用い、特性
向上をはかっている。In these examples, in order to suppress the deterioration of light resistance due to titanium oxide, the surface of titanium oxide particles is coated with optically stable silicon dioxide, or a silicon-based coupling agent and colloidal silica are used as a binder to improve the characteristics. I'm thinking.
しかし、これらの従来技術のうち、酸化チタン粒子表面
を二酸化ケイ素で被覆する方法では、酸化チタン粒子径
が数百ミクロン以上のものについては効果的であるが、
本発明で述べる微粒子の場合、表面積が大きく、粒子表
面を充分被覆出来ないという問題点を有する。However, among these conventional techniques, the method of coating the surface of titanium oxide particles with silicon dioxide is effective for titanium oxide particles having a diameter of several hundreds of microns or more,
In the case of the fine particles described in the present invention, there is a problem that the surface area is large and the particle surface cannot be sufficiently covered.
また、後者の例では、シリコン系カップリング剤の一部
の劣化、および基材が、合成樹脂の場合、基材との界面
が光により劣化し、塗膜剥れが発生するという問題を有
する。Further, in the latter example, there is a problem that part of the silicon-based coupling agent deteriorates, and when the base material is a synthetic resin, the interface with the base material is deteriorated by light and coating film peeling occurs. .
そこで本発明は、このような問題点を解決するもので、
その目的とするところは、耐摩耗性,紫外線遮蔽,耐薬
品性を有し、且つ、耐候性あるいは耐光性に優れた塗料
組成物およびその得られる透明性塗膜を提供するところ
にある。Therefore, the present invention solves such a problem,
An object of the invention is to provide a coating composition having abrasion resistance, ultraviolet ray shielding property, chemical resistance, and excellent weather resistance or light resistance, and a transparent coating film obtained from the coating composition.
本発明の酸化チタンを含有する塗料は、酸化チタン微粒
子を含むバインダービヒクル中に、少なくとも下記の成
分(A)または(B)を一種以上含むことを特徴とす
る。The coating material containing titanium oxide of the present invention is characterized in that the binder vehicle containing titanium oxide fine particles contains at least one or more of the following components (A) or (B).
(A)Co,Pd,Ag,Cr,Pb,Cu,V,Pt,W,Hg,La,Bi,Moから選ば
れる金属アセチルアセトンもくは金属アセト酢酸エステ
ルの配位化合物 (B)Co,Pd,Ag,Cr,Pb,Cu,V,Pt,W,Hg,La,Bi,Moから選ば
れる金属アラコラート化合物 更に詳細に説明する。(A) Coordination compound of metal acetylacetone or metal acetoacetate selected from Co, Pd, Ag, Cr, Pb, Cu, V, Pt, W, Hg, La, Bi, Mo (B) Co, Pd , Metal aracholate compound selected from Ag, Cr, Pb, Cu, V, Pt, W, Hg, La, Bi and Mo will be described in more detail.
ここで用いる酸化チタン微粒子は、その粒径は1ないし
100ミリミクロンのものが適している。粒径1ミリミク
ロン以下では、充分な耐摩耗性,紫外線遮蔽効果が得ら
れず、また、粒径が100ミリミクロン以上では、得られ
た塗膜は白濁し、透明性が低下すると同時に、耐光性が
低下する。The titanium oxide fine particles used here have a particle size of 1 to
The one of 100 mm is suitable. If the particle size is 1 millimicron or less, sufficient abrasion resistance and ultraviolet ray shielding effect cannot be obtained, and if the particle size is 100 millimicron or more, the obtained coating film becomes cloudy and the transparency decreases and at the same time the light resistance is reduced. Sex decreases.
次に本発明に用いる金属種をもつ有機化合物としては、
Co,Pd,Ag,Cr,Pb,Cu,V,Pt,W,Hg,La,Bi,Moから選ばれる金
属アセチルアセトン、金属アセト酢酸メチル、アセト酢
酸エチル,アセト酢酸プロピルのキレート化合物、また
Co,Pd,Ag,Cr,Pb,Cu,V,Pt,W,Hg,La,Bi,Moから選ばれるア
セテート、プロピオネート、ブチレート、ラクテート、
エトキシド、ブトキシドのアルコラートが挙げられる。
これらの中でも、アセチルアセトネート、アセト酢酸エ
ステルの配位子をもつ化合物は、水や温度に安定な為、
特に好ましい。Next, as the organic compound having a metal species used in the present invention,
Metal acetylacetone selected from Co, Pd, Ag, Cr, Pb, Cu, V, Pt, W, Hg, La, Bi, Mo, methyl acetoacetate acetate, chelate compound of ethyl acetoacetate, propyl acetoacetate, or
Co, Pd, Ag, Cr, Pb, Cu, V, Pt, W, Hg, La, Bi, Mo selected from acetate, propionate, butyrate, lactate,
Examples thereof include alcoholates of ethoxide and butoxide.
Among these, compounds having ligands of acetylacetonate and acetoacetate are stable in water and temperature,
Particularly preferred.
この金属化合物の添加量は、チタン原子に対し金属原子
が重量比で、100ppmから、10%の範囲で添加出来る。10
0ppm以下では、効果が得られず、また10%以上では、塗
液の調合が困難となってくる為好ましくない。The metal compound can be added in a weight ratio of titanium atom to metal atom of 100 ppm to 10%. Ten
If it is 0 ppm or less, the effect cannot be obtained, and if it is 10% or more, it becomes difficult to prepare a coating solution, which is not preferable.
次に、バインダビヒクルとして用いる材料としては、シ
ランカップリング剤,酸化ケイ素ゾルや合成高分子,天
然高分子,変成天然高分子あるいは反応性モノマー等が
ある。また、増粘剤,フローコントロール剤,レベリン
グ剤,溶剤,染料等の一種以上から構成される。Next, examples of the material used as the binder vehicle include a silane coupling agent, a silicon oxide sol, a synthetic polymer, a natural polymer, a modified natural polymer or a reactive monomer. Further, it is composed of one or more of a thickener, a flow control agent, a leveling agent, a solvent, a dye and the like.
ここで、シラン化合物は例えば、一般式 で表わされるシランカップリング剤や、テトラアルコキ
シシラン等がある。これらの加水分解物,部分縮合物等
も同等の性質を有する。Here, the silane compound has, for example, a general formula There are silane coupling agents represented by and tetraalkoxysilanes. These hydrolyzates and partial condensates have the same properties.
ここでR1は、アルキル基,アルケニル基,フエニル基,
ハロゲン基等,またR2は、エポキシ基,アミノ基,アミ
ド基,メルカプト基,メタクリロイルオキシ基,シアノ
基,核ハロゲン化芳香環を有する基等を含む有機基を示
し、Xは、ハロゲン基,アルコキシル基,アルケノキシ
基,アルコキシアルコキシル基,アシルオキシ基等の加
水分解可能な基を示す。また、a,bは、各々0,1または2
で、a+bが1ないし3である。これらの化合物の例と
しては、テトラメトキシシラン等の四官能シラン,メチ
ルトリメトキシシラン,γ−クロロプロピルトリメトキ
シシラン,ビニルトリメトキシシラン,γ−メタクリロ
イルオキシプロピルトリメトキシシラン,β−(3,4−
エポキシシクロヘキシル)エチルトリメトキシシラン,
γ−グリシドキシプロピルトリメトキシシラン,γ−メ
ルカプトプロピルトリメトキシシラン,γ−アミノプロ
ピルトリメトキシシラン,N−β−(アミノエチル)−γ
−アミノプロピルトリメトキシシラン,γ−ウレイドプ
ロピルトリメトキシシラン,γ−シアノプロピルトリメ
トキシシラン,γ−モルフオリノプロピルトリメトキシ
シラン,N−フエニルアミノプロピルトリメトキシシラン
等の三官能シラン、前記三官能シランの一部がメチル
基,エチル基,ビニル基に置換した二官能シラン等が挙
げられる。Here, R 1 is an alkyl group, an alkenyl group, a phenyl group,
A halogen group or the like, R 2 is an organic group including an epoxy group, an amino group, an amide group, a mercapto group, a methacryloyloxy group, a cyano group, a group having a nuclear halogenated aromatic ring, X is a halogen group, It shows a hydrolyzable group such as an alkoxyl group, an alkenoxy group, an alkoxyalkoxyl group, and an acyloxy group. Also, a and b are 0, 1 or 2 respectively.
And a + b is 1 to 3. Examples of these compounds include tetrafunctional silanes such as tetramethoxysilane, methyltrimethoxysilane, γ-chloropropyltrimethoxysilane, vinyltrimethoxysilane, γ-methacryloyloxypropyltrimethoxysilane, β- (3,4 −
Epoxycyclohexyl) ethyltrimethoxysilane,
γ-glycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-aminopropyltrimethoxysilane, N-β- (aminoethyl) -γ
-Aminopropyltrimethoxysilane, γ-ureidopropyltrimethoxysilane, γ-cyanopropyltrimethoxysilane, γ-morpholinopropyltrimethoxysilane, N-phenylaminopropyltrimethoxysilane and other trifunctional silanes, A bifunctional silane in which a part of the functional silane is replaced with a methyl group, an ethyl group, or a vinyl group can be used.
また、有機性バインダ成分の例としては、高分子体のも
のでは、カルボキシアルキル化セルロース等のセルロー
ス類,テルペン系樹脂,グルコース誘導体,ポリアミノ
酸,キチン,キトサン類,デンプン類の天然高分子や、
ポリビニルアルコール,ポリエチレングリコール,ポリ
アクリル酸,ポリアクリル酸エステル,ポリメタクリル
酸エステル,ポリビニルアミン,ポリウレタン,ポリビ
ニルピロリドン,ポリビニルピリジン,ポリビニルイミ
ダゾール等の極性基を有する合成高分子や、ポリスチレ
ン,ビスフエノールA,ポリカーボネート等の含芳香族高
分子や、ポリサルフオン類の機能性樹脂,変成フッ素系
高分子等がある。Examples of the organic binder component include polymers such as carboxyalkylated celluloses, terpene resins, glucose derivatives, polyamino acids, chitins, chitosans, and natural polymers such as starches.
Synthetic polymers with polar groups such as polyvinyl alcohol, polyethylene glycol, polyacrylic acid, polyacrylic acid ester, polymethacrylic acid ester, polyvinylamine, polyurethane, polyvinylpyrrolidone, polyvinylpyridine, polyvinylimidazole, polystyrene, bisphenol A, Examples include aromatic polymers such as polycarbonate, functional resins such as polysulfones, and modified fluorine-based polymers.
また、反応性モノマーあるいはオリゴマーの例として
は、光硬化可能な多官能アクリレートや、エチレングリ
コールジグリシジルエーテル等のエポキシ化合物,ラク
トン等の開環重合性モノマー,イソシアネート類等の反
応性モノマーを挙げることができる。Examples of reactive monomers or oligomers include photocurable polyfunctional acrylates, epoxy compounds such as ethylene glycol diglycidyl ether, ring-opening polymerizable monomers such as lactones, and reactive monomers such as isocyanates. You can
塗液は、アルコール類,エステル類,ケトン類,セロソ
ルブ類,ホルムアミド類や水,フレオン等の溶剤によ
り希釈された、1〜20重量%の固型分を含む溶液が好適
であるが、必ずしも限定されるものではない。The coating liquid is preferably a solution containing 1 to 20% by weight of a solid component diluted with a solvent such as alcohols, esters, ketones, cellosolves, formamides, water, and Freon, but not always limited. It is not something that will be done.
次に、塗膜を得る方法としては、各種の塗布法を用いる
ことができる。また、乾燥と硬化は、例えば40〜200℃
で10分〜10時間の加熱方法が適当であるが、この他に
も、赤外線,紫外線,γ線,電子線照射等のプロセスも
必要に応じて用いることができる。Next, as a method for obtaining a coating film, various coating methods can be used. Also, drying and curing is, for example, 40-200 ℃
A heating method of 10 minutes to 10 hours is suitable, but in addition to this, processes such as infrared ray, ultraviolet ray, γ-ray and electron beam irradiation can also be used if necessary.
このようにして得られる酸化チタンを含有する塗膜につ
き、 イ 耐光性の向上 ロ 透明性の確保 の作用つき説明する。The coating film containing titanium oxide obtained in this manner will be described below with respect to the function of improving light resistance and ensuring transparency.
即ち、イの耐光性については、詳細な原理は不明である
が、酸化チタンの光触媒効果が幾つか報告されている
(例えば、G.N.Schrauzer and T.D.Guth,J.Am.Chem、So
c.,99,7189(1977))。本発明は、酸化チタン微粒子に
光触媒活性をも活性点があると考え、各種金属種を添加
し、特に効果のあった金属を見出したものである。従つ
て、メカニズムとしてはこれらの金属あるいは金属キレ
ート化合物類が、酸化チタンの光活性点の近く、あるい
は、弱い結合を伴って塗膜中に存在し、光触媒能、すな
わち光エネルギーの化学エネルギーへの変換を防げてい
ると推測出来る。言い換えれば、酸化チタンのもつ光触
媒能は、光エネルギーを化学エネルギーに変換し、化学
的な活性種を作りだすものでありこれが、酸化チタンを
含む塗膜のビヒクルの化学結合を切断,変質させるもの
であったと考えられる。そして、本発明は酸化チタンの
もつ光エネルギーの化学エネルギーへの変換過程の抑制
か、または、変換された光エネルギーを熱エネルギーと
することにより、酸化還元能を抑制したものと考えられ
る。即ち、加えた金属種のこのような作用により、塗膜
の耐光性を向上させたものである。That is, regarding the light resistance of (i), although the detailed principle is unknown, some photocatalytic effects of titanium oxide have been reported (for example, GN Schrauzer and TDGuth, J. Am. Chem, So.
c., 99 , 7189 (1977)). The present invention considers that titanium oxide fine particles also have an active site for photocatalytic activity, and has added various metal species, and found a metal that is particularly effective. Therefore, as a mechanism, these metals or metal chelate compounds are present in the coating film near the photoactive point of titanium oxide or with a weak bond, and the photocatalytic ability, that is, the conversion of light energy into chemical energy is performed. You can guess that it can prevent the conversion. In other words, the photocatalytic ability of titanium oxide converts light energy into chemical energy to create chemically active species, which cuts or modifies the chemical bonds of the vehicle of the coating film containing titanium oxide. I think it was. It is considered that the present invention suppresses the redox ability by suppressing the conversion process of light energy of titanium oxide into chemical energy or by converting the converted light energy into heat energy. That is, the light resistance of the coating film is improved by such an action of the added metal species.
ロ 透明性の確保については、酸化チタンの粒型を100
ミリミクロン以下にすることにより、粒子表面の乱反射
を抑え透明性を増すことができた。透過率を高めようと
する光の波長と粒径は、コロイド化学において相関性が
見出されている(例えば、H.Weller et.al.,Chem.Phys.
Letters,124,557(1986)。本発明は、バインダビヒク
ルに均等に酸化チタンおよび金属種を分散させた場合可
視光の波長域で透明性に問題のないレベルを検討し見出
したもので、引用例では、10ミリミクロン以下の粒径が
必要とあるが、酸化チタン粒子を所定の粒径とし、且つ
バインダ中へ均質に分散させることにより、粒子と高分
子の界面の反射が、許容出来る範囲を見出したものであ
る。(B) To ensure transparency, use a titanium oxide particle type of 100
By setting the particle size to be less than or equal to millimicrons, it was possible to suppress irregular reflection on the particle surface and increase transparency. Correlation has been found in colloid chemistry between the wavelength of light that seeks to increase transmittance and particle size (e.g., H. Weller et.al., Chem. Phys.
Letters, 124 , 557 (1986). The present invention was found by investigating a level where there is no problem in transparency in the wavelength range of visible light when titanium oxide and metal species are evenly dispersed in the binder vehicle, and in the cited example, particles of 10 mm or less are used. Although the diameter is required, it has been found that the reflection at the interface between the particles and the polymer is within an allowable range by making the titanium oxide particles have a predetermined particle diameter and uniformly dispersing the particles in the binder.
以下、実施例により本発明を更に詳しく説明するが、こ
れらは本発明を限定するものではない。Hereinafter, the present invention will be described in more detail with reference to Examples, but these do not limit the present invention.
尚、実施例中、部は重量部を表わす。In the examples, “part” means “part by weight”.
実施例1 (1) 酸化チタンを含有する塗料の調整 マグネット撹拌子による撹拌装置を有するガラス製フラ
スコ内に、二酸化チタン水性ゾル(粒径10ミリミクロ
ン,固型分10重量%,水分散コロイド)10部を入れ、充
分撹拌を行いつつ、水15部、続いて、エチルセルソルブ
15部を加え、酸化チタンコロイド液とした。Example 1 (1) Preparation of Paint Containing Titanium Oxide Titanium dioxide aqueous sol (particle size: 10 millimicrons, solid content: 10% by weight, aqueous dispersion colloid) was placed in a glass flask having a stirring device with a magnetic stirrer. Add 10 parts of water, mix well, and mix with 15 parts of water, followed by ethyl cellosolve.
15 parts were added to obtain a titanium oxide colloidal solution.
ここに、コバルトIIアセチルアセトネート2水和物0.15
部を、アセチルアセトン2部,エチルセロソルブ8部に
溶解させた溶液を、ゆっくり加え、コバルト原子を含む
コロイド分散液とした。この分散液中、チタン原子に対
するコバルト含有量は、5重量%である。Cobalt II acetylacetonate dihydrate 0.15
A solution prepared by dissolving 2 parts of acetylacetone in 8 parts of ethyl cellosolve was slowly added to obtain a colloidal dispersion containing cobalt atoms. In this dispersion, the cobalt content with respect to titanium atoms is 5% by weight.
次に混合するバインダビヒクルを含む液は次のように調
合した。即ち、反応用フラスコ内において、γ−グリシ
ドキシプロピルトリメトキシシラン1.5部,エチルセロ
ソルブ20部,0.1規定塩酸水1.0部を撹拌混合し、シラン
化合物の加水分解を行い、バインダ溶液とした。The liquid containing the binder vehicle to be mixed next was prepared as follows. That is, in a reaction flask, 1.5 parts of γ-glycidoxypropyltrimethoxysilane, 20 parts of ethyl cellosolve, and 1.0 part of 0.1N hydrochloric acid water were stirred and mixed to hydrolyze the silane compound to obtain a binder solution.
このバインダ溶液を、先の酸化チタンコロイド液中に、
撹拌下、ゆっくりと加えたのち、シリコン系界面活性剤
を少量加え、塗布用の塗料とした。This binder solution is added to the titanium oxide colloidal solution,
After slowly adding with stirring, a small amount of a silicon-based surfactant was added to obtain a coating material for coating.
(2) 塗料の塗布・硬化による塗膜の形成 このようにして得られた塗料は、酸素プラズマにより10
秒間処理されたポリカーボネートパネル板に、スピンコ
ート法により塗布を行ったのち100℃で3時間乾燥およ
び硬化させることにより均質な塗膜を得た。(2) Forming a coating film by coating and curing the paint
A polycarbonate panel plate treated for seconds was applied by a spin coating method and then dried and cured at 100 ° C. for 3 hours to obtain a uniform coating film.
(3) 塗膜の評価試験と結果 このようにして得られた複合体は以下の手順で評価試験
を行った。(3) Evaluation Test of Coating Film and Results The composite thus obtained was evaluated by the following procedure.
耐摩耗性:1cm×3cmの大きさのテストピースの表面を
スチールウール(#0000)にて、1cm2あたり100gの荷重
をかけ10往復摩擦したときの傷のつき具合を目視で判定
した。評価ランク基準は以下の通りである。Abrasion resistance: The surface of a test piece having a size of 1 cm x 3 cm was visually inspected with a steel wool (# 0000) to apply a load of 100 g per 1 cm 2 and rub it for 10 reciprocations. The evaluation rank criteria are as follows.
A:1cm×3cmの範囲に傷がつかない。A: No scratches in the area of 1 cm x 3 cm.
B:上記範囲内に1〜10本の傷がつく。B: 1 to 10 scratches are made within the above range.
C:上記範囲内に10〜100本の傷がつく。C: 10 to 100 scratches are made within the above range.
D:無数の傷がついているが、平滑な表面が残っている。D: There are countless scratches, but there is still a smooth surface.
E:表面についた傷のため平滑な表面は残っていない。E: No smooth surface remains due to scratches on the surface.
耐熱水性:レンズを沸騰している純水に1時間浸漬し
た後、前記と同様に耐摩耗性の試験を行なった。Hot water resistance: The lens was immersed in boiling pure water for 1 hour, and then tested for abrasion resistance in the same manner as above.
耐薬品性:4%水酸化ナトリウム水溶液中に1時間浸漬
後のテストピースの外観および10%塩酸中に10時間浸漬
後の外観を評価した。Chemical resistance: The appearance of the test piece after immersion in a 4% aqueous sodium hydroxide solution for 1 hour and the appearance after immersion in 10% hydrochloric acid for 10 hours were evaluated.
耐光性(耐候性):キセノンランプフエードメーター
(スガ試験機 FAL−25AX型)で光暴露100時間後の塗膜
の変化を調べ評価した。Light resistance (weather resistance): A xenon lamp fade meter (Suga Tester FAL-25AX type) was used to evaluate the change in the coating film after 100 hours of light exposure.
密着性:いわゆるクロスカットテープテストで、ナイ
フで直交する1mm間隔の11本の平行な切り傷をいれ、1mm
3の100個のマス目をつくる。次に、粘着テープ(商品名
“セロテープ”)を強くはりつけ、90゜方向に急速には
がし、残ったマス目を分子に、分母に総マス目をとって
密着性の指標とした。Adhesion: In the so-called cross-cut tape test, 11 parallel cuts were made at a 1 mm interval perpendicular to each other with a knife, and 1 mm
Make 100 squares of 3 . Next, an adhesive tape (trade name "Cellotape") was strongly adhered and rapidly peeled in the direction of 90 °, and the remaining squares were used as numerator and the denominator was taken as the total square to be used as an index of adhesion.
本実施例を、以上の評価方法に基づき試験を行った結
果、 耐摩耗性:B 耐熱水性:異常なし 耐薬品性:異常なし 耐光性:硬さがBからCにやや低下外観および,
の試験では異常なし 密着性:100/100で良好 であった。また、塗膜は透明であり、耐光性試験後も濁
り、黄変の発生や密着性の低下が見られず良好なもので
あった。特に基材であるポリカーボネートは、そのまま
では、やや黄変したが本実施例のテストピースでは、こ
のような黄変が殆んどみられないことから、紫外線遮蔽
性にすぐれたものと推測出来た。As a result of conducting a test based on the above evaluation method, this example shows that abrasion resistance: B, hot water resistance: no abnormality, chemical resistance: no abnormality, light resistance: hardness slightly decreases from B to C, appearance, and
In the test, there was no abnormality. Adhesion: 100/100 was good. Further, the coating film was transparent and was good without turbidity even after the light resistance test, no yellowing and no decrease in adhesion were observed. In particular, the polycarbonate, which is the base material, slightly yellowed as it was, but in the test piece of this example, such yellowing was hardly seen, so it can be assumed that it has excellent ultraviolet shielding properties. .
この複合体は、市販の分散染料による染色も可能で装飾
パネルとしても有用であった。This composite was dyeable with a commercially available disperse dye and was useful as a decorative panel.
実施例2,3 実施例1において、基材をアルミ板,ポリジエチレング
リコールビスアリルカーボネートレンズにかえること以
外は、実施例1と同様に塗膜形成を行い、良好な外観の
複合体が得られた。この複合体の耐光性も良好であっ
た。Examples 2 and 3 In Example 1, a coating film was formed in the same manner as in Example 1 except that the substrate was changed to an aluminum plate and a polydiethylene glycol bisallyl carbonate lens, and a composite having a good appearance was obtained. . The light resistance of this composite was also good.
実施例4〜12・比較例1〜7 実施例1において、コバルトIIアセチルアセトネート2
水和物0.15部のかわりに、第1表に示す金属化合物を用
い、その使用量は、塗膜組成物中で各金属原子がチタン
原子の5重量%を占めるように設定すること以外は、実
施例1と同様にして塗料の調整と塗膜の形成を行った。
このようにして得られた複合体の評価は実施例1の手順
に従って実施し、得られた試験結果を第2表に示した。Examples 4-12 and Comparative Examples 1-7 In Example 1, cobalt II acetylacetonate 2
Instead of 0.15 parts of the hydrate, the metal compounds shown in Table 1 were used, and the amount used was set such that each metal atom accounted for 5% by weight of titanium atom in the coating composition. The coating material was adjusted and the coating film was formed in the same manner as in Example 1.
The composite thus obtained was evaluated according to the procedure of Example 1, and the test results obtained are shown in Table 2.
〔発明の効果〕 本発明は、酸化チタンを含む塗料中に、銅,バナジウ
ム,鉛等の特定の金属イオンの配位化合物あるいは有機
基含有化合物を含むことにより、酸化チタンの光触媒能
に対する触媒毒として作用させるもので、結果として、
塗膜の耐光性を向上させることができるという効果が得
られた。この効果を応用し、各種の塗料添加物へ酸化チ
タンを混入し光特性を向上させる場合に応用し耐久性,
耐光性を増すことに役立つ。これらの塗料は、保護コー
トとして、耐摩耗性,耐薬品性,耐水性をを向上させ、
また、汚れ防止、美観向上の為の付加価値をもたせるた
めに有用である。特にこの高屈折率である特徴を生かし
て、低屈折率薄膜と組みあわせることによって得られる
反射防止膜はプラスチックフィルム,プラスチックパネ
ル,プラスチックレンズ等のプラスチック製光学材料を
はじめガラスパネル等へも応用が可能である。その他、
ディスク,パネル,構造用部材,光学部品等の用途があ
る。 [Advantages of the Invention] The present invention provides a catalyst poison for the photocatalytic activity of titanium oxide by containing a coordination compound or an organic group-containing compound of a specific metal ion such as copper, vanadium, or lead in a coating material containing titanium oxide. As a result,
The effect that the light resistance of the coating film can be improved was obtained. Applying this effect, when applying titanium oxide to various paint additives to improve optical characteristics, durability,
Helps increase lightfastness. These paints, as a protective coat, improve wear resistance, chemical resistance, and water resistance,
In addition, it is useful for preventing stains and adding value for improving aesthetics. In particular, taking advantage of this characteristic of high refractive index, the antireflection film obtained by combining it with a low refractive index thin film can be applied to plastic films, plastic panels, plastic optical materials such as plastic lenses, and glass panels. It is possible. Other,
There are applications such as disks, panels, structural members, and optical parts.
Claims (2)
ル中に、少なくとも下記の成分(A)または(B)を一
種以上含むことを特徴とする酸化チタンを含有する塗
料。 (A)Co,Pd,Ag,Cr,Pb,Cu,V,Pt,W,Hg,La,Bi,Moから選ば
れる金属アセチルアセトンもくは金属アセト酢酸エステ
ルの配位化合物 (B)Co,Pd,Ag,Cr,Pb,Cu,V,Pt,W,Hg,La,Bi,Moから選ば
れる金属アルコラート化合物1. A coating material containing titanium oxide, characterized in that a binder vehicle containing fine particles of titanium oxide contains at least one or more of the following components (A) or (B). (A) Coordination compound of metal acetylacetone or metal acetoacetate selected from Co, Pd, Ag, Cr, Pb, Cu, V, Pt, W, Hg, La, Bi, Mo (B) Co, Pd , Alcolate compounds selected from Ag, Cr, Pb, Cu, V, Pt, W, Hg, La, Bi and Mo
クロンであることを特徴とする特許請求の範囲第1項記
載の酸化チタンを含有する塗料。2. The coating material containing titanium oxide according to claim 1, wherein the titanium oxide fine particles have a particle diameter of 1 to 100 millimicrons.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62058252A JPH0788491B2 (en) | 1987-03-13 | 1987-03-13 | Paint containing titanium oxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62058252A JPH0788491B2 (en) | 1987-03-13 | 1987-03-13 | Paint containing titanium oxide |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63223076A JPS63223076A (en) | 1988-09-16 |
JPH0788491B2 true JPH0788491B2 (en) | 1995-09-27 |
Family
ID=13078943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62058252A Expired - Lifetime JPH0788491B2 (en) | 1987-03-13 | 1987-03-13 | Paint containing titanium oxide |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0788491B2 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3794837B2 (en) * | 1998-10-27 | 2006-07-12 | 長島特殊塗料株式会社 | Thermal barrier paint and coating method thereof |
US6703131B1 (en) | 1999-06-24 | 2004-03-09 | Nippon Arc Co., Ltd. | Coated article |
KR100400999B1 (en) * | 2000-10-09 | 2003-10-10 | (주) 나노팩 | A coating composition for blocking UV which comprises Fe ion-doped Titanium dioxide photocatalyst |
JP2004027241A (en) * | 2003-10-14 | 2004-01-29 | Nagashima Tokushu Toryo Kk | Thermal insulation coating and its coating method |
GB2454132B (en) * | 2006-08-24 | 2011-11-23 | Ngimat Co | Optical coating |
JP4700587B2 (en) * | 2006-10-12 | 2011-06-15 | Hoya株式会社 | Test condition determination method and test method for adhesion performance of titanium-based hard coat with lens base material |
JP2014038293A (en) * | 2012-08-20 | 2014-02-27 | Nissan Chem Ind Ltd | Dispersion liquid of titanium oxide-based fine particles, coating composition including particles and base material with transparent film |
WO2014080606A1 (en) * | 2012-11-22 | 2014-05-30 | パナソニック株式会社 | Optical semiconductor dispersed resin composition, method for producing same, and antibacterial member |
JP6019056B2 (en) * | 2014-03-28 | 2016-11-02 | 大日本塗料株式会社 | SUBSTRATE WITH LAMINATED COATING AND COATING COMPOSITION FOR FORMING PRIMER LAYER FOR FORMING THE LAMINATED COATING |
-
1987
- 1987-03-13 JP JP62058252A patent/JPH0788491B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS63223076A (en) | 1988-09-16 |
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