JPH10337526A - Method for forming photocatalytic-hydrophilic coat, base material cleaning agent for forming photocatalytic-hydrophilic coat and material for forming photocatalytic-hydrophilic coat - Google Patents
Method for forming photocatalytic-hydrophilic coat, base material cleaning agent for forming photocatalytic-hydrophilic coat and material for forming photocatalytic-hydrophilic coatInfo
- Publication number
- JPH10337526A JPH10337526A JP10112787A JP11278798A JPH10337526A JP H10337526 A JPH10337526 A JP H10337526A JP 10112787 A JP10112787 A JP 10112787A JP 11278798 A JP11278798 A JP 11278798A JP H10337526 A JPH10337526 A JP H10337526A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- forming
- coating
- substrate
- 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.)
- Granted
Links
- 239000012459 cleaning agent Substances 0.000 title claims abstract description 61
- 239000000463 material Substances 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title claims description 34
- 238000000576 coating method Methods 0.000 claims abstract description 218
- 239000011248 coating agent Substances 0.000 claims abstract description 207
- 239000007788 liquid Substances 0.000 claims abstract description 85
- 230000001699 photocatalysis Effects 0.000 claims abstract description 67
- 239000002245 particle Substances 0.000 claims abstract description 53
- 238000004140 cleaning Methods 0.000 claims abstract description 23
- 239000004094 surface-active agent Substances 0.000 claims abstract description 14
- 239000002253 acid Substances 0.000 claims abstract description 9
- 229920002050 silicone resin Polymers 0.000 claims abstract description 4
- 239000011941 photocatalyst Substances 0.000 claims description 77
- 239000000758 substrate Substances 0.000 claims description 48
- 239000005357 flat glass Substances 0.000 claims description 42
- 239000000203 mixture Substances 0.000 claims description 37
- 238000005406 washing Methods 0.000 claims description 31
- 229920001296 polysiloxane Polymers 0.000 claims description 27
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 21
- 239000003599 detergent Substances 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 17
- 159000000007 calcium salts Chemical class 0.000 claims description 12
- 230000001443 photoexcitation Effects 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 239000011521 glass Substances 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 10
- 125000000962 organic group Chemical group 0.000 claims description 9
- 239000002736 nonionic surfactant Substances 0.000 claims description 8
- 239000003566 sealing material Substances 0.000 claims description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000000356 contaminant Substances 0.000 claims description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 5
- 230000001678 irradiating effect Effects 0.000 claims description 4
- KVBCYCWRDBDGBG-UHFFFAOYSA-N azane;dihydrofluoride Chemical compound [NH4+].F.[F-] KVBCYCWRDBDGBG-UHFFFAOYSA-N 0.000 claims description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 2
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 238000007146 photocatalysis Methods 0.000 claims description 2
- VBKNTGMWIPUCRF-UHFFFAOYSA-M potassium;fluoride;hydrofluoride Chemical compound F.[F-].[K+] VBKNTGMWIPUCRF-UHFFFAOYSA-M 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 142
- 239000004744 fabric Substances 0.000 abstract description 30
- 239000002585 base Substances 0.000 abstract description 29
- 230000000873 masking effect Effects 0.000 abstract description 22
- 230000000694 effects Effects 0.000 abstract description 15
- 229920005989 resin Polymers 0.000 abstract description 8
- 239000011347 resin Substances 0.000 abstract description 8
- 239000002689 soil Substances 0.000 abstract description 3
- 239000003513 alkali Substances 0.000 abstract description 2
- 230000003197 catalytic effect Effects 0.000 abstract description 2
- 230000003647 oxidation Effects 0.000 abstract description 2
- 238000007254 oxidation reaction Methods 0.000 abstract description 2
- 229920001187 thermosetting polymer Polymers 0.000 abstract description 2
- 230000002411 adverse Effects 0.000 abstract 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 135
- -1 polyoxyethylene Polymers 0.000 description 100
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 73
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 59
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 50
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 48
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 47
- 229910017604 nitric acid Inorganic materials 0.000 description 47
- 239000000243 solution Substances 0.000 description 45
- 239000007864 aqueous solution Substances 0.000 description 37
- 238000001035 drying Methods 0.000 description 26
- 238000005507 spraying Methods 0.000 description 25
- 239000003973 paint Substances 0.000 description 24
- 238000007865 diluting Methods 0.000 description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 16
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000007921 spray Substances 0.000 description 14
- 239000003981 vehicle Substances 0.000 description 14
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 13
- 239000011734 sodium Substances 0.000 description 12
- 229910052708 sodium Inorganic materials 0.000 description 12
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 11
- 239000008399 tap water Substances 0.000 description 10
- 235000020679 tap water Nutrition 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 239000008199 coating composition Substances 0.000 description 8
- 238000001723 curing Methods 0.000 description 8
- 239000002344 surface layer Substances 0.000 description 8
- 239000002699 waste material Substances 0.000 description 8
- 229910000420 cerium oxide Inorganic materials 0.000 description 7
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 150000004756 silanes Chemical class 0.000 description 6
- 229920001214 Polysorbate 60 Polymers 0.000 description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
- 230000001771 impaired effect Effects 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 238000010422 painting Methods 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000004115 Sodium Silicate Substances 0.000 description 3
- MZZINWWGSYUHGU-UHFFFAOYSA-J ToTo-1 Chemical compound [I-].[I-].[I-].[I-].C12=CC=CC=C2C(C=C2N(C3=CC=CC=C3S2)C)=CC=[N+]1CCC[N+](C)(C)CCC[N+](C)(C)CCC[N+](C1=CC=CC=C11)=CC=C1C=C1N(C)C2=CC=CC=C2S1 MZZINWWGSYUHGU-UHFFFAOYSA-J 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000008119 colloidal silica Substances 0.000 description 3
- 239000004567 concrete Substances 0.000 description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
- 230000005284 excitation Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000011344 liquid material Substances 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 238000012643 polycondensation polymerization Methods 0.000 description 3
- 239000000565 sealant Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000004590 silicone sealant Substances 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 229910052911 sodium silicate Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- 229940054273 1-propoxy-2-propanol Drugs 0.000 description 2
- FENFUOGYJVOCRY-UHFFFAOYSA-N 1-propoxypropan-2-ol Chemical compound CCCOCC(C)O FENFUOGYJVOCRY-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 2
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 2
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 2
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- LWZFANDGMFTDAV-BURFUSLBSA-N [(2r)-2-[(2r,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O LWZFANDGMFTDAV-BURFUSLBSA-N 0.000 description 2
- 239000003082 abrasive agent Substances 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- 235000012216 bentonite Nutrition 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- VGWJKDPTLUDSJT-UHFFFAOYSA-N diethyl dimethyl silicate Chemical compound CCO[Si](OC)(OC)OCC VGWJKDPTLUDSJT-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000002070 germicidal effect Effects 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 230000003405 preventing effect Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 229910052604 silicate mineral Inorganic materials 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 235000011008 sodium phosphates Nutrition 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 229950006451 sorbitan laurate Drugs 0.000 description 2
- 235000011067 sorbitan monolaureate Nutrition 0.000 description 2
- 229950004959 sorbitan oleate Drugs 0.000 description 2
- 229950003429 sorbitan palmitate Drugs 0.000 description 2
- 229950011392 sorbitan stearate Drugs 0.000 description 2
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 2
- UQMOLLPKNHFRAC-UHFFFAOYSA-N tetrabutyl silicate Chemical compound CCCCO[Si](OCCCC)(OCCCC)OCCCC UQMOLLPKNHFRAC-UHFFFAOYSA-N 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten trioxide Chemical compound O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 0.000 description 2
- 229910052724 xenon Inorganic materials 0.000 description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- 229910052845 zircon Inorganic materials 0.000 description 2
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 2
- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 1
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 description 1
- 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 1
- LPMBTLLQQJBUOO-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCO)CCO LPMBTLLQQJBUOO-KTKRTIGZSA-N 0.000 description 1
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- FMVOPJLFZGSYOS-UHFFFAOYSA-N 2-[2-(2-ethoxypropoxy)propoxy]propan-1-ol Chemical compound CCOC(C)COC(C)COC(C)CO FMVOPJLFZGSYOS-UHFFFAOYSA-N 0.000 description 1
- WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 description 1
- WADSJYLPJPTMLN-UHFFFAOYSA-N 3-(cycloundecen-1-yl)-1,2-diazacycloundec-2-ene Chemical compound C1CCCCCCCCC=C1C1=NNCCCCCCCC1 WADSJYLPJPTMLN-UHFFFAOYSA-N 0.000 description 1
- XBIUWALDKXACEA-UHFFFAOYSA-N 3-[bis(2,4-dioxopentan-3-yl)alumanyl]pentane-2,4-dione Chemical compound CC(=O)C(C(C)=O)[Al](C(C(C)=O)C(C)=O)C(C(C)=O)C(C)=O XBIUWALDKXACEA-UHFFFAOYSA-N 0.000 description 1
- ZYAASQNKCWTPKI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propan-1-amine Chemical compound CO[Si](C)(OC)CCCN ZYAASQNKCWTPKI-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
- KBQVDAIIQCXKPI-UHFFFAOYSA-N 3-trimethoxysilylpropyl prop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C=C KBQVDAIIQCXKPI-UHFFFAOYSA-N 0.000 description 1
- MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-UHFFFAOYSA-N 0.000 description 1
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical class COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 1
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 235000011430 Malus pumila Nutrition 0.000 description 1
- 235000015103 Malus silvestris Nutrition 0.000 description 1
- AOMUHOFOVNGZAN-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 1
- BACYUWVYYTXETD-UHFFFAOYSA-N N-Lauroylsarcosine Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 description 1
- DIOYAVUHUXAUPX-KHPPLWFESA-N Oleoyl sarcosine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC(O)=O DIOYAVUHUXAUPX-KHPPLWFESA-N 0.000 description 1
- 230000010802 Oxidation-Reduction Activity Effects 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920006197 POE laurate Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241001074085 Scophthalmus aquosus Species 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- ZIQPQYFSSSHQBP-UHFFFAOYSA-N acetyl 2,3-dihydroxypropanoate Chemical compound CC(=O)OC(=O)C(O)CO ZIQPQYFSSSHQBP-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 125000005667 alkyl propylene group Chemical group 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229940009868 aluminum magnesium silicate Drugs 0.000 description 1
- WMGSQTMJHBYJMQ-UHFFFAOYSA-N aluminum;magnesium;silicate Chemical compound [Mg+2].[Al+3].[O-][Si]([O-])([O-])[O-] WMGSQTMJHBYJMQ-UHFFFAOYSA-N 0.000 description 1
- ZRGUXTGDSGGHLR-UHFFFAOYSA-K aluminum;triperchlorate Chemical compound [Al+3].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O ZRGUXTGDSGGHLR-UHFFFAOYSA-K 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- YSJGOMATDFSEED-UHFFFAOYSA-M behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 1
- YSALUHGLIBYTET-UHFFFAOYSA-N benzyl(dibutoxy)silane Chemical compound CCCCO[SiH](OCCCC)CC1=CC=CC=C1 YSALUHGLIBYTET-UHFFFAOYSA-N 0.000 description 1
- OCBHHZMJRVXXQK-UHFFFAOYSA-M benzyl-dimethyl-tetradecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 OCBHHZMJRVXXQK-UHFFFAOYSA-M 0.000 description 1
- WMWLMWRWZQELOS-UHFFFAOYSA-N bismuth(III) oxide Inorganic materials O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- JUNWLZAGQLJVLR-UHFFFAOYSA-J calcium diphosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])(=O)OP([O-])([O-])=O JUNWLZAGQLJVLR-UHFFFAOYSA-J 0.000 description 1
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 229940043256 calcium pyrophosphate Drugs 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- FJDJVBXSSLDNJB-LNTINUHCSA-N cobalt;(z)-4-hydroxypent-3-en-2-one Chemical compound [Co].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FJDJVBXSSLDNJB-LNTINUHCSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002772 conduction electron Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- MGQFVQQCNPBJKC-UHFFFAOYSA-N dibutoxy(diethyl)silane Chemical compound CCCCO[Si](CC)(CC)OCCCC MGQFVQQCNPBJKC-UHFFFAOYSA-N 0.000 description 1
- GQNWJCQWBFHQAO-UHFFFAOYSA-N dibutoxy(dimethyl)silane Chemical compound CCCCO[Si](C)(C)OCCCC GQNWJCQWBFHQAO-UHFFFAOYSA-N 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 235000019821 dicalcium diphosphate Nutrition 0.000 description 1
- 235000019700 dicalcium phosphate Nutrition 0.000 description 1
- 229960004670 didecyldimethylammonium chloride Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- ZMAPKOCENOWQRE-UHFFFAOYSA-N diethoxy(diethyl)silane Chemical compound CCO[Si](CC)(CC)OCC ZMAPKOCENOWQRE-UHFFFAOYSA-N 0.000 description 1
- MNFGEHQPOWJJBH-UHFFFAOYSA-N diethoxy-methyl-phenylsilane Chemical compound CCO[Si](C)(OCC)C1=CC=CC=C1 MNFGEHQPOWJJBH-UHFFFAOYSA-N 0.000 description 1
- VSYLGGHSEIWGJV-UHFFFAOYSA-N diethyl(dimethoxy)silane Chemical compound CC[Si](CC)(OC)OC VSYLGGHSEIWGJV-UHFFFAOYSA-N 0.000 description 1
- BZCJJERBERAQKQ-UHFFFAOYSA-N diethyl(dipropoxy)silane Chemical compound CCCO[Si](CC)(CC)OCCC BZCJJERBERAQKQ-UHFFFAOYSA-N 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 1
- CVQVSVBUMVSJES-UHFFFAOYSA-N dimethoxy-methyl-phenylsilane Chemical compound CO[Si](C)(OC)C1=CC=CC=C1 CVQVSVBUMVSJES-UHFFFAOYSA-N 0.000 description 1
- ZIDTUTFKRRXWTK-UHFFFAOYSA-N dimethyl(dipropoxy)silane Chemical compound CCCO[Si](C)(C)OCCC ZIDTUTFKRRXWTK-UHFFFAOYSA-N 0.000 description 1
- UAKOZKUVZRMOFN-JDVCJPALSA-M dimethyl-bis[(z)-octadec-9-enyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+](C)(C)CCCCCCCC\C=C/CCCCCCCC UAKOZKUVZRMOFN-JDVCJPALSA-M 0.000 description 1
- YYLGKUPAFFKGRQ-UHFFFAOYSA-N dimethyldiethoxysilane Chemical compound CCO[Si](C)(C)OCC YYLGKUPAFFKGRQ-UHFFFAOYSA-N 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 229940079886 disodium lauryl sulfosuccinate Drugs 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
- KHIQYZGEUSTKSB-UHFFFAOYSA-L disodium;4-dodecoxy-4-oxo-3-sulfobutanoate Chemical compound [Na+].[Na+].CCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC([O-])=O.CCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC([O-])=O KHIQYZGEUSTKSB-UHFFFAOYSA-L 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- KUCGHDUQOVVQED-UHFFFAOYSA-N ethyl(tripropoxy)silane Chemical compound CCCO[Si](CC)(OCCC)OCCC KUCGHDUQOVVQED-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 235000013611 frozen food Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229940031957 lauric acid diethanolamide Drugs 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- RJMRIDVWCWSWFR-UHFFFAOYSA-N methyl(tripropoxy)silane Chemical compound CCCO[Si](C)(OCCC)OCCC RJMRIDVWCWSWFR-UHFFFAOYSA-N 0.000 description 1
- JQYGMRTZHJTQAC-UHFFFAOYSA-N methyl-phenyl-dipropoxysilane Chemical compound CCCO[Si](C)(OCCC)C1=CC=CC=C1 JQYGMRTZHJTQAC-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- UPHWVVKYDQHTCF-UHFFFAOYSA-N octadecylazanium;acetate Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCCN UPHWVVKYDQHTCF-UHFFFAOYSA-N 0.000 description 1
- 229920002114 octoxynol-9 Polymers 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- FABOKLHQXVRECE-UHFFFAOYSA-N phenyl(tripropoxy)silane Chemical compound CCCO[Si](OCCC)(OCCC)C1=CC=CC=C1 FABOKLHQXVRECE-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- WFIZEGIEIOHZCP-UHFFFAOYSA-M potassium formate Chemical compound [K+].[O-]C=O WFIZEGIEIOHZCP-UHFFFAOYSA-M 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- BWILYWWHXDGKQA-UHFFFAOYSA-M potassium propanoate Chemical compound [K+].CCC([O-])=O BWILYWWHXDGKQA-UHFFFAOYSA-M 0.000 description 1
- 239000004331 potassium propionate Substances 0.000 description 1
- 235000010332 potassium propionate Nutrition 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- FOWDZVNRQHPXDO-UHFFFAOYSA-N propyl hydrogen carbonate Chemical compound CCCOC(O)=O FOWDZVNRQHPXDO-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010458 rotten stone Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 235000019794 sodium silicate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- CAVXVRQDZKMZDB-UHFFFAOYSA-M sodium;2-[dodecanoyl(methyl)amino]ethanesulfonate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CCS([O-])(=O)=O CAVXVRQDZKMZDB-UHFFFAOYSA-M 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- VDWRUZRMNKZIAJ-UHFFFAOYSA-N tetradecylazanium;acetate Chemical compound CC(O)=O.CCCCCCCCCCCCCCN VDWRUZRMNKZIAJ-UHFFFAOYSA-N 0.000 description 1
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- GIHPVQDFBJMUAO-UHFFFAOYSA-N tributoxy(ethyl)silane Chemical compound CCCCO[Si](CC)(OCCCC)OCCCC GIHPVQDFBJMUAO-UHFFFAOYSA-N 0.000 description 1
- GYZQBXUDWTVJDF-UHFFFAOYSA-N tributoxy(methyl)silane Chemical compound CCCCO[Si](C)(OCCCC)OCCCC GYZQBXUDWTVJDF-UHFFFAOYSA-N 0.000 description 1
- INUOIYMEJLOQFN-UHFFFAOYSA-N tributoxy(phenyl)silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)C1=CC=CC=C1 INUOIYMEJLOQFN-UHFFFAOYSA-N 0.000 description 1
- WAAWAIHPWOJHJJ-UHFFFAOYSA-N tributoxy(propyl)silane Chemical compound CCCCO[Si](CCC)(OCCCC)OCCCC WAAWAIHPWOJHJJ-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- VUWVDNLZJXLQPT-UHFFFAOYSA-N tripropoxy(propyl)silane Chemical compound CCCO[Si](CCC)(OCCC)OCCC VUWVDNLZJXLQPT-UHFFFAOYSA-N 0.000 description 1
- DAOVYDBYKGXFOB-UHFFFAOYSA-N tris(2-methylpropoxy)alumane Chemical compound [Al+3].CC(C)C[O-].CC(C)C[O-].CC(C)C[O-] DAOVYDBYKGXFOB-UHFFFAOYSA-N 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000021269 warm food Nutrition 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- Catalysts (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、基材表面を高度の
親水性になし、かつ維持することの可能な塗膜を形成す
るための方法に関する。特に既設の基材に上記塗膜を形
成するための好適な方法に関する。さらには、既設の浴
室用部材、エアコン室外機、便器のように難溶性カルシ
ウム塩に起因する汚れが付着している基材に上記塗膜を
形成するための好適な方法に関する。 さらには、既設
の窓ガラス、窓枠、外壁のようにシリコーンシーリング
材に起因する汚れが付着している基材や、永久汚れが付
着している窓ガラスに上記塗膜を形成するための好適な
方法に関する。また本発明は、特に既設の基材表面を高
度の親水性になし、かつ維持することの可能な塗膜を形
成するにあたり、その表面を清浄化するための洗浄剤、
コーティング組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for forming a coating film capable of making a substrate surface highly hydrophilic and maintaining it. Particularly, the present invention relates to a suitable method for forming the coating film on an existing substrate. Furthermore, the present invention relates to a suitable method for forming the coating film on a base material such as an existing bathroom member, an air conditioner outdoor unit, and a toilet on which dirt caused by a hardly soluble calcium salt is adhered. Furthermore, suitable for forming the above-mentioned coating film on an existing window glass, a window frame, a substrate to which dirt caused by a silicone sealing material is attached such as an outer wall, or a window glass to which permanent dirt is attached. About the method. In addition, the present invention, particularly to make the existing substrate surface highly hydrophilic, and forming a coating film that can be maintained, a cleaning agent for cleaning the surface,
It relates to a coating composition.
【0002】[0002]
【従来の技術】本発明者らは、PCT/WO96/29
375号に開示したように、基材表面に光触媒含有層を
形成すると、光触媒の光励起に応じて前記層表面が、水
との接触角に換算して10゜以下という高度の親水性を
呈することを見出し、さらにそれによりガラス、レン
ズ、鏡等の透明部材の防曇・視界確保性向上、物品表面
の水洗浄性・降雨洗浄性向上等の効果が得られることを
見出した。2. Description of the Related Art The present inventors have proposed PCT / WO96 / 29.
As disclosed in Japanese Patent No. 375, when a photocatalyst-containing layer is formed on a substrate surface, the layer surface exhibits a high degree of hydrophilicity of 10 ° or less in terms of a contact angle with water in response to photoexcitation of the photocatalyst. Further, it has been found that such effects as anti-fogging and improving visibility of transparent members such as glass, lenses, mirrors, and the like, and improving water washability and rainfall washability of the article surface can be obtained.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、特に既
設の基材上に上記層を形成しようとすると、既設の基材
表面に既に汚れが付着しているために、その汚れの影響
で表面の透明性、意匠性や親水性が損なわれることがあ
った。本発明の目的は、上記事情に鑑みてなされたもの
であり、既設の基材の汚れの影響で表面の透明性、意匠
性や親水性が損なわれることのない光触媒性親水性被膜
の形成方法を提供することにある。本発明の他の目的
は、表面の透明性、意匠性や親水性が損なわれることの
ない光触媒性親水性被膜を形成するための洗浄剤ならび
光触媒性親水性被膜形成用材料を提供することにある。However, in particular, when the above-mentioned layer is formed on an existing base material, since the surface of the existing base material is already contaminated, the surface becomes transparent due to the influence of the contaminant. Properties, design properties and hydrophilicity were sometimes impaired. An object of the present invention has been made in view of the above circumstances, and a method for forming a photocatalytic hydrophilic film in which the transparency, design, and hydrophilicity of the surface are not impaired by the influence of dirt on an existing substrate. Is to provide. Another object of the present invention is to provide a photocatalytic hydrophilic film forming material as well as a detergent for forming a photocatalytic hydrophilic film without impairing the surface transparency, design and hydrophilicity. is there.
【0004】[0004]
【課題を解決するための手段】本発明では、上記課題を
解決すべく、基材表面を洗浄する工程を行った後に、光
触媒性親水性コ−ティング液を塗布し、硬化せしめるこ
とを特徴とする光触媒性親水性被膜の形成方法を提供す
る。基材表面を洗浄することにより、既設の基材の汚れ
を除去することができるので、既設の基材の汚れの影響
で表面の親水性が損なわれることを防止することが可能
となる。In order to solve the above-mentioned problems, the present invention is characterized in that after performing a step of cleaning the surface of a substrate, a photocatalytic hydrophilic coating liquid is applied and cured. The present invention provides a method for forming a photocatalytic hydrophilic coating. By cleaning the surface of the base material, dirt on the existing base material can be removed, so that it is possible to prevent the hydrophilicity of the surface from being impaired by the influence of the dirt on the existing base material.
【0005】本発明の一態様においては、前記光触媒性
親水性コ−ティング液は、平均組成式SiXqO(4-q)/2
(式中、Xはアルコキシ基、又は、ハロゲン原子であ
り、qは0<q<4を満足する数である)で表されるシ
リケ−トからなる塗膜形成要素であって、硬化させると
無定型シリカの被膜を形成するもの、及び前記塗膜形成
要素中に分散され、光励起に応じて前記被膜の表面を親
水化するための光触媒性酸化物粒子を含有するようにす
る。係るコ−ティング液により基材表面に塗膜を形成す
ると、無定型シリカの硬化反応により、常温から150
℃程度の低温で、基材表面には光触媒性酸化物粒子と無
定型シリカを含有する被膜が形成されるようになる。従
って、既設の基材に光触媒性親水性被膜を容易に形成で
きる。[0005] In one embodiment of the present invention, the photocatalytic hydrophilic coating liquid has an average composition formula of Si x q O (4-q) / 2.
(Where X is an alkoxy group or a halogen atom, and q is a number satisfying 0 <q <4). It contains an amorphous silica coating and photocatalytic oxide particles dispersed in the coating-forming element to hydrophilize the surface of the coating in response to photoexcitation. When a coating film is formed on the substrate surface with the coating liquid, a curing reaction of the amorphous silica causes the coating solution to be heated from room temperature to 150 ° C.
At a low temperature of about ° C., a film containing photocatalytic oxide particles and amorphous silica is formed on the substrate surface. Therefore, the photocatalytic hydrophilic film can be easily formed on the existing base material.
【0006】本発明の他の態様においては、前記光触媒
性親水性コ−ティング液は、平均組成式RpSiXqO
(4-p-q)/2(式中、Rは一価の有機基の1種若しくは2
種以上からなる官能基、又は、一価の有機基と水素基か
ら選ばれた2種以上からなる官能基であり、Xはアルコ
キシ基、又は、ハロゲン原子であり、p及びqは0<p
<2、0<q<4を満足する数である)で表されるシロ
キサンからなる塗膜形成要素であって、硬化させるとシ
リコ−ン樹脂の被膜を形成するもの、及び前記塗膜形成
要素中に分散され、光励起によって前記被膜の表面のシ
リコ−ン分子中のケイ素原子に結合した有機基を光触媒
作用により少なくとも部分的に水酸基に置換させ、さら
に光励起に応じて被膜の表面を親水化するための光触媒
性酸化物粒子を含有するようにする。係るコ−ティング
液により基材表面に塗膜を形成すると、シロキサンの硬
化反応により、常温から150℃程度の低温で、基材表
面には光触媒性酸化物粒子とシリコーンを含有する被膜
が形成されるようになる。従って、既設の基材に光触媒
性親水性被膜を容易に形成できる。[0006] In another aspect of the present invention, the photocatalytic hydrophilic co - coating solution, the average composition formula R p SiX q O
(4-pq) / 2 (wherein R is one or more monovalent organic groups)
X is an alkoxy group or a halogen atom, and p and q are 0 <p.
<2, 0 <q <4), a film-forming element comprising a siloxane represented by the following formula: which, when cured, forms a silicone resin film; The organic group dispersed in the silicon film on the surface of the film by photoexcitation is at least partially replaced with a hydroxyl group by photocatalysis, and the surface of the film is hydrophilized by photoexcitation. To contain photocatalytic oxide particles. When a coating film is formed on the surface of the substrate with the coating liquid, a coating containing photocatalytic oxide particles and silicone is formed on the surface of the substrate at a low temperature of from room temperature to about 150 ° C. due to a siloxane curing reaction. Become so. Therefore, the photocatalytic hydrophilic film can be easily formed on the existing base material.
【0007】本発明の他の態様においては、シリコ−ン
シ−リング材に起因する汚れが付着した基材表面に光触
媒性親水性被膜の形成方法する方法であって、その方法
は基材表面を洗浄液で洗浄して有色の汚れ成分を除去す
る工程、残留シリコ−ン上をプライマ−により被覆する
工程を行った後に、光触媒性親水性コ−ティング液を塗
布し硬化せしめることを特徴とする光触媒性親水性被膜
の形成方法を提供する。 残留シリコ−ン上をプライマ
−により被覆して、表面を親水性にすることにより、光
触媒性親水性コ−ティング液が基材表面に濡れるように
なり、均一な光触媒性親水性被膜が形成されるようにな
るので、既設の基材のシリコ−ン汚れの影響で表面の親
水性が損なわれることを防止することが可能となる。In another aspect of the present invention, there is provided a method for forming a photocatalytic hydrophilic coating on a surface of a substrate to which dirt caused by a silicone sealing material has adhered, the method comprising: A photocatalyst characterized by applying a photocatalytic hydrophilic coating liquid and curing after performing a step of removing colored contaminants by washing with a cleaning liquid and a step of coating the remaining silicone with a primer. Provided is a method for forming a hydrophilic hydrophilic film. By coating the remaining silicone with a primer to make the surface hydrophilic, the photocatalytic hydrophilic coating liquid becomes wet on the substrate surface, and a uniform photocatalytic hydrophilic coating is formed. As a result, it is possible to prevent the hydrophilicity of the surface from being impaired due to the influence of silicone contamination on the existing base material.
【0008】本発明の他の態様においては、シリコ−ン
シ−リング材に起因する汚れが付着した基材表面に光触
媒性親水性被膜の形成方法する方法であって、その方法
は基材表面を洗浄液で洗浄して有色の汚れ成分を除去す
る工程、残留シリコ−ン表面に紫外線を照射する工程を
行った後に、光触媒性親水性コ−ティング液を塗布し硬
化せしめることを特徴とする光触媒性親水性被膜の形成
方法を提供する。残留シリコ−ン上に紫外線を照射する
ことにより被覆して、表面を親水性にすることにより、
光触媒性親水性コ−ティング液が基材表面に濡れるよう
になり、均一な光触媒性親水性被膜が形成されるように
なるので、既設の基材のシリコ−ン汚れの影響で表面の
親水性が損なわれることを防止することが可能となる。[0008] In another aspect of the present invention, there is provided a method for forming a photocatalytic hydrophilic film on a surface of a substrate to which dirt caused by a silicone sealing material has adhered, the method comprising: A photocatalytic property characterized by applying a photocatalytic hydrophilic coating liquid and curing after performing a step of removing colored stain components by washing with a cleaning liquid, and a step of irradiating a residual silicon surface with ultraviolet rays. Provided is a method for forming a hydrophilic coating. By coating the residual silicone by irradiating ultraviolet rays to make the surface hydrophilic,
The photocatalytic hydrophilic coating liquid becomes wet on the surface of the base material, and a uniform photocatalytic hydrophilic film is formed. Therefore, the hydrophilicity of the surface is affected by the influence of the silicone stain on the existing base material. Can be prevented from being damaged.
【0009】[0009]
【発明の実施の形態】基材表面を洗浄する工程は、例え
ば、以下の手順で行う。まず、洗浄液及びその後に塗布
する光触媒性親水性コ−ティング液の塗布部周辺への飛
散を防止するために、塗布部周辺部をマスキングする。
次いで、洗浄剤を含浸させた布、ウエス、脱脂綿等で拭
いて、基材表面に付着している汚れを除去する。ここ
で、洗浄剤には、界面活性剤、酸、アルカリ、等が適宜
利用できる。また、上記洗浄剤に研磨剤を配合させても
よい。次に、水を含浸させた布、ウエス、脱脂綿等で拭
いて、基材表面に残存する洗浄剤を除去する。次に、ワ
イパ−や乾いた布、ウエス、脱脂綿等で、水を拭き取
る。BEST MODE FOR CARRYING OUT THE INVENTION The step of cleaning the surface of a substrate is performed, for example, in the following procedure. First, in order to prevent the washing liquid and the photocatalytic hydrophilic coating liquid to be applied thereafter from scattering around the applied part, the peripheral part of the applied part is masked.
Next, the dirt adhering to the surface of the base material is removed by wiping with a cloth impregnated with a cleaning agent, a rag, absorbent cotton, or the like. Here, a surfactant, an acid, an alkali, or the like can be appropriately used as the cleaning agent. Moreover, you may mix | blend an abrasive with the said cleaning agent. Next, a cleaning agent remaining on the surface of the base material is removed by wiping with a cloth impregnated with water, a rag, absorbent cotton, or the like. Next, the water is wiped off with a wiper, a dry cloth, a rag, absorbent cotton, or the like.
【0010】洗浄剤は、基材の種類や汚れに応じて、酸
性洗浄剤、塩基性洗浄剤、界面活性剤や研磨剤を配合さ
せた洗浄剤、有機溶剤等が適宜利用できる。2種類以上
の洗浄剤を組み合わせて利用しても良い。難溶性カルシ
ウム塩に起因する汚れや、シリカゲルを主成分とする窓
ガラスの永久汚れを除去するためには酸性洗浄剤が好適
に利用できる。酸性洗浄剤に利用できる酸としては、硫
酸、硝酸、塩酸、リン酸、弗化水素、酸性弗化アンモニ
ウム、酸性弗化カリウム等の無機酸や、ぎ酸、酢酸、シ
ュウ酸、クエン酸、リンゴ酸、コハク酸、スルファミン
酸、グリコール酸、グルコン酸等の有機酸が挙げられ
る。油性汚れの除去には塩基性洗浄剤や界面活性剤を配
合させた洗浄剤が好適に利用できる。塩基性洗浄剤に利
用される塩基としては、水酸化ナトリウム、水酸化カリ
ウム、炭酸ナトリウム、珪酸ナトリウム、リン酸ナトリ
ウム、アンモニア水、モノエタノールアミン、ジエタノ
ールアミン、トリエタノールアミンや、アルカリ電解水
等が挙げられる。界面活性剤としては、スルホン酸ポリ
オキシエチレンアルキルフェニルエ−テルアンモニウム
塩、スルホン酸ポリオキシエチレンアルキルフェニルエ
−テルナトリウム塩、脂肪酸カリセッケン、脂肪酸ナト
リウムセッケン、ジオクチルスルホコハク酸ナトリウ
ム、アルキルサルフェ−ト、アルキルエ−テルサルフェ
−ト、アルキルサルフェ−トソ−ダ塩、アルキルエ−テ
ルサルフェ−トソ−ダ塩、ポリオキシエチレンアルキル
エ−テルサルフェ−ト、ポリオキシエチレンアルキルエ
−テルサルフェ−トソ−ダ塩、アルキルサルフェ−トT
EA塩、ポリオキシエチレンアルキルエ−テルサルフェ
−トTEA塩、2−エチルヘキシルアルキル硫酸エステ
ルナトリウム塩、アシルメチルタウリン酸ナトリウム、
ラウロイルメチルタウリン酸ナトリウム、ドデシルベン
ゼンスルホン酸ナトリウム、アルキルベンゼンスルホン
酸ナトリウム、スルホコハク酸ラウリル2ナトリウム、
ポリオキシエチレンスルホコハク酸ラウリル2ナトリウ
ム、ポリカルボン酸、オレオイルザルコシン、アミドエ
−テルサルフェ−ト、ラウロイルザルコシネ−ト、スル
ホFAエステルナトリウム塩、パーフルオロアルキルス
ルホン酸塩、パーフルオロアルキルカルボン酸塩、パー
フルオロアルキルリン酸塩、パーフルオロアルケニルオ
キシベンゼンスルホン酸ナトリウム、パーフルオロアル
ケニルオキシベンゼンスルホニルサルコシンナトリウ
ム、パーフルオロアルケニルオキシアラルキルホスホン
酸、等のアニオン性界面活性剤;ポリオキシエチレンラ
ウリルエ−テル、ポリオキシエチレントリデシルエ−テ
ル、ポリオキシエチレンアセチルエ−テル、ポリオキシ
エチレンステアリルエ−テル、ポリオキシエチレンオレ
イルエ−テル、ポリオキシエチレンアルキルエ−テル、
ポリオキシエチレンアルキルエステル、ポリオキシエチ
レンアルキルフェノ−ルエ−テル、ポリオキシエチレン
ノニルフェニルエ−テル、ポリオキシエチレンオクチル
フェニルエ−テル、ポリオキシエチレンラウラ−ト、ポ
リオキシエチレンステアレ−ト、ポリオキシエチレンア
ルキルフェニルエ−テル、ポリオキシエチレンオレエ−
ト、ソルビタンアルキルエステル、ポリオキシエチレン
ソルビタンアルキルエステル、ポリエ−テル変性シリコ
−ン、ポリエステル変性シリコ−ン、ソルビタンラウラ
−ト、ソルビタンステアレ−ト、ソルビタンパルミテ−
ト、ソルビタンセスキオレエ−ト、ソルビタンオレエ−
ト、ポリオキシエチレンソルビタンラウラ−ト、ポリオ
キシエチレンソルビタンステアレ−ト、ポリオキシエチ
レンソルビタンパルミテ−ト、ポリオキシエチレンソル
ビタンオレエ−ト、グリセロ−ルステアレ−ト、ポリグ
リセリン脂肪酸エステル、アルキルアルキロ−ルアミ
ド、ラウリン酸ジエタノ−ルアミド、オレイン酸ジエタ
ノ−ルアミド、オキシエチレンドデシルアミン、ポリオ
キシエチレンドデシルアミン、ポリオキシエチレンアル
キルアミン、ポリオキシエチレンオクタデシルアミン、
ポリオキシエチレンアルキルプロピレンジアミン、ポリ
オキシエチレンオキシプロピレンブロックポリマ−、ポ
リオキシエチレンステアレ−ト、パーフルオロアルキル
エチレンオキシド付加物、パーフルオロアルキルエチレ
ンオキシド・プロピレンオキシド付加物、パーフルオロ
アルキルプロピレンオキシド付加物、パーフルオロアル
キルオリゴマー、パーフルオロアルケニルポリオキシエ
チレンエーテル、パーフルオロアルケニルオキシオキシ
エチレンエーテル、ジグリセリンテトラキス(パーフル
オロアルケニルオキシオキシエチレンエーテル)等のノ
ニオン性界面活性剤;ジメチルアルキルベタイン、アル
キルグリシン、アミドベタイン、イミダゾリン、パーフ
ルオロアルキルアミノスルホン酸塩、パーフルオロアル
キルベタイン、パーフルオロアルケニルオキシアラルキ
ルベタイン等の両性界面活性剤;オクタデシルジメチル
ベンジルアンモニウムクロライド、アルキルジメチルベ
ンジルアンモニウムクロライド、テトラデシルジメチル
ベンジルアンモニウムクロライド、ジオレイルジメチル
アンモニウムクロライド、1−ヒドロキシ−2−アルキ
ルイミダゾリン4級塩、アルキルイソキノリニウムブロ
マイド、高分子アミン、オクタデシルトリメチルアンモ
ニウムクロライド、アルキルトリメチルアンモニウムク
ロライド、ドデシルトリメチルアンモニウムクロライ
ド、ヘキサデシルトリメチルアンモニウムクロライド、
ベヘニルトリメチルアンモニウムクロライド、アルキル
イミダゾリン4級塩、ジアルキルジメチルアンモニウム
クロライド、オクタデシルアミン酢酸塩、テトラデシル
アミン酢酸塩、アルキルプロピレンジアミン酢酸塩、ジ
デシルジメチルアンモニウムクロライド、パーフルオロ
アルキルトリメチルアンモニウム塩、パーフルオロアル
キル第4級アンモニウム塩、パーフルオロアルケニルオ
キシベンゼンスルホンアルキルアンモニウムヨージド、
パーフルオロアルケニルオキシベンズアミドアルキルア
ンモニウムヨージド等のカチオン性界面活性剤等が利用
できる。洗浄性を高めるために、洗浄剤に研磨剤を配合
しても良い。研磨剤としては、酸化セリウム、けい石
粉、トリポリ、ドロマイト、珪藻土、酸化アルミニウ
ム、アルミナ、シリカ、タルク、カオリン、ベントナイ
ト、リン酸水素カルシウム、炭酸カルシウム、含水ケイ
酸、珪酸アルミニウム、珪石、炭化珪素、水酸化アルミ
ニウム、メタリン酸ナトリウム、リン酸カルシウム、ピ
ロリン酸カルシウム、ゼオライト、ジルコンサンド、酸
化ジルコン、珪酸ジルコニア、ガラス粉、パーライト、
酸化マグネシウム、活性白土、酸性白土、酸化チタン、
酸化鉄、酸化クロム、酸化亜鉛、ダイヤモンドパウダ
ー、チッ化ホウ素、炭化ホウ素、等が利用できる。これ
ら研磨剤の平均粒子径は0.01〜100μm、好まし
くは0.01〜10μmが良い。洗浄剤の構成成分とし
ては、上記の成分以外にも、ビルダー、安定剤、溶剤、
可溶化剤等が挙げられる。ビルダーとしては、炭酸ナト
リウム、リン酸ナトリウム、リン酸カリウム、メタ珪酸
ナトリウム、珪酸ナトリウム、ゼオライト、トリポリリ
ン酸ナトリウム、ピロリン酸カリウム、硫酸ナトリウ
ム、クエン酸ナトリウム、エチレンジアミン4酢酸ナト
リウム、ニトリロ3酢酸ナトリウム、3−オキサペンタ
ン酸ナトリウム、ポリアクリル酸ナトリウム、アクリル
酸/メタクリル酸共重合体ナトリウム塩、アクリル酸/
マレイン酸共重合体ナトリウム塩、カルボキシメチルセ
ルロースナトリウム塩等が利用できる。安定剤として
は、カルボキシメチルセルロースナトリウム塩、メチル
セルロース、エチルセルロース、ヒドロキシエチルセル
ロース、ポリエチレングリコール、カルボキシビニルポ
リマー、ポリアクリル酸塩、ポリアクリルアミド、ポリ
ビニルアルコール、ポリビニルピロリドン、ポリビニル
アセテート鹸化物、キサンタンガム、グアーガム、アル
ギン酸ナトリウム、アラビアゴム、寒天、ゼラチン、ペ
クチン、デキストリン、デンプン、リグニンスルフォン
酸塩、酢酸ビニル、イソブチルマレイン酸共重合物、カ
ルボン酸塩、珪酸アルミニウムマグネシウム、珪酸マグ
ネシウム、ベントナイト、モンモリロナイト、アタパル
ジャイト、セピオライト等が利用できる。溶剤として
は、水のほか、メタノール、エタノール、イソプロパノ
ール、ノルマルプロパノール、イソブタノール、エチレ
ングリコール、プロピレングリコール等のアルコール
類、アセトン、メチルエチルケトン、メチルプロピルケ
トン、メチルブチルケトン、ジプロピルケトン等のケト
ン類、酢酸エチル、酢酸プロピル、酢酸イソプロピル、
酢酸ブチル、酢酸アミル、酪酸エチル等のエステル類、
n−ヘキサン、シクロヘキサン、ヘプタン等の炭化水素
類、ケロシン、ホワイトスピリット、ミネラルスピリッ
ト、ナフサ等の石油類、ジエチレングリコール、エチレ
ングリコールアルキルエーテル、ジエチレングリコール
アルキルエーテル、オリゴエチレングリコールアルキル
エーテル、ジプロピレングリコール、プロピレングリコ
ールアルキルエーテル、ジプロピレングリコールアルキ
ルエーテル、オリゴプロピレングリコールアルキルエー
テル、等のグリコール系溶媒やグリセリン等が利用でき
る。可溶化剤としては、パラトルエンスルホン酸、スル
ホコハク酸ナトリウム等が利用できる。As the cleaning agent, an acidic cleaning agent, a basic cleaning agent, a cleaning agent containing a surfactant or an abrasive, an organic solvent, and the like can be appropriately used depending on the type and stain of the base material. Two or more cleaning agents may be used in combination. In order to remove stains caused by the hardly soluble calcium salt and permanent stains on window glass mainly composed of silica gel, an acidic cleaning agent can be suitably used. Acids that can be used for the acidic cleaning agent include inorganic acids such as sulfuric acid, nitric acid, hydrochloric acid, phosphoric acid, hydrogen fluoride, ammonium fluoride and potassium fluoride, formic acid, acetic acid, oxalic acid, citric acid, and apple. Organic acids such as acid, succinic acid, sulfamic acid, glycolic acid, gluconic acid and the like can be mentioned. For removing oily stains, a detergent containing a basic detergent or a surfactant can be suitably used. Examples of the base used for the basic detergent include sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, sodium phosphate, aqueous ammonia, monoethanolamine, diethanolamine, triethanolamine, and alkaline electrolyzed water. Can be Examples of the surfactant include polyoxyethylene alkyl phenyl ether ammonium sulphonate, sodium polyoxyethylene alkyl phenyl ether sulphonate, fatty acid soap, fatty acid sodium soap, sodium dioctyl sulfosuccinate, alkyl sulfate, Alkyl ether sulfate, alkyl sulfate soda salt, alkyl ether sulfate soda salt, polyoxyethylene alkyl ether sulfate, polyoxyethylene alkyl ether sulfate soda salt, alkyl sulfate -T
EA salt, polyoxyethylene alkyl ether tersulfate TEA salt, 2-ethylhexylalkyl sulfate sodium salt, sodium acylmethyltaurate,
Sodium lauroylmethyltaurate, sodium dodecylbenzenesulfonate, sodium alkylbenzenesulfonate, disodium lauryl sulfosuccinate,
Disodium lauryl polyoxyethylene sulfosuccinate, polycarboxylic acid, oleoyl sarcosine, amido ether sulphate, lauroyl sarcosine, sodium sulfo FA ester, perfluoroalkyl sulfonate, perfluoroalkyl carboxylate Anionic surfactants such as perfluoroalkyl phosphate, sodium perfluoroalkenyloxybenzenesulfonate, sodium perfluoroalkenyloxybenzenesulfonylsarcosine, perfluoroalkenyloxyaralkylphosphonic acid, and the like; polyoxyethylene lauryl ether; Polyoxyethylene tridecyl ether, polyoxyethylene acetyl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether, poly Carboxymethyl ethylene alkyl ET - ethers,
Polyoxyethylene alkyl ester, polyoxyethylene alkyl phenol ether, polyoxyethylene nonylphenyl ether, polyoxyethylene octylphenyl ether, polyoxyethylene laurate, polyoxyethylene stearate, poly Oxyethylene alkylphenyl ether, polyoxyethylene oleate
Sorbitan alkyl ester, polyoxyethylene sorbitan alkyl ester, polyether modified silicone, polyester modified silicone, sorbitan laurate, sorbitan stearate, sorbitan palmitate
, Sorbitan sesquioleate, sorbitan oleate
Polyoxyethylene sorbitan laurate, polyoxyethylene sorbitan stearate, polyoxyethylene sorbitan palmitate, polyoxyethylene sorbitan oleate, glycerol stearate, polyglycerin fatty acid ester, alkyl alcohol Kiloamide, lauric acid diethanolamide, oleic acid diethanolamide, oxyethylene dodecylamine, polyoxyethylene dodecylamine, polyoxyethylene alkylamine, polyoxyethylene octadecylamine,
Polyoxyethylene alkyl propylene diamine, polyoxyethylene oxypropylene block polymer, polyoxyethylene stearate, perfluoroalkyl ethylene oxide adduct, perfluoroalkyl ethylene oxide / propylene oxide adduct, perfluoroalkyl propylene oxide adduct, Nonionic surfactants such as fluoroalkyl oligomers, perfluoroalkenyl polyoxyethylene ether, perfluoroalkenyloxyoxyethylene ether, and diglycerin tetrakis (perfluoroalkenyloxyoxyethylene ether); dimethylalkyl betaine, alkyl glycine, amido betaine; Imidazoline, perfluoroalkylaminosulfonate, perfluoroalkylbetaine, Amphoteric surfactants such as fluoroalkenyloxyaralkylbetaine; octadecyldimethylbenzylammonium chloride, alkyldimethylbenzylammonium chloride, tetradecyldimethylbenzylammonium chloride, dioleyldimethylammonium chloride, 1-hydroxy-2-alkylimidazoline quaternary salt, alkyl Isoquinolinium bromide, polymeric amine, octadecyltrimethylammonium chloride, alkyltrimethylammonium chloride, dodecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride,
Behenyltrimethylammonium chloride, alkylimidazoline quaternary salt, dialkyldimethylammonium chloride, octadecylamine acetate, tetradecylamine acetate, alkylpropylenediamine acetate, didecyldimethylammonium chloride, perfluoroalkyltrimethylammonium salt, perfluoroalkyl Quaternary ammonium salts, perfluoroalkenyloxybenzenesulfonalkylammonium iodides,
Cationic surfactants such as perfluoroalkenyloxybenzamide alkylammonium iodide and the like can be used. An abrasive may be added to the cleaning agent in order to enhance the cleaning performance. As abrasives, cerium oxide, silica powder, tripoli, dolomite, diatomaceous earth, aluminum oxide, alumina, silica, talc, kaolin, bentonite, calcium hydrogen phosphate, calcium carbonate, hydrous silicate, aluminum silicate, silica, silicon carbide, Aluminum hydroxide, sodium metaphosphate, calcium phosphate, calcium pyrophosphate, zeolite, zircon sand, zircon oxide, zirconia silicate, glass powder, perlite,
Magnesium oxide, activated clay, acid clay, titanium oxide,
Iron oxide, chromium oxide, zinc oxide, diamond powder, boron nitride, boron carbide, and the like can be used. The average particle size of these abrasives is 0.01 to 100 μm, and preferably 0.01 to 10 μm. As components of the detergent, in addition to the above components, builders, stabilizers, solvents,
And solubilizers. Builders include sodium carbonate, sodium phosphate, potassium phosphate, sodium metasilicate, sodium silicate, zeolite, sodium tripolyphosphate, potassium pyrophosphate, sodium sulfate, sodium citrate, sodium ethylenediaminetetraacetate, sodium nitrilotriacetate, Sodium oxapentanate, sodium polyacrylate, sodium salt of acrylic acid / methacrylic acid copolymer, acrylic acid /
Maleic acid copolymer sodium salt, carboxymethyl cellulose sodium salt and the like can be used. As a stabilizer, carboxymethylcellulose sodium salt, methylcellulose, ethylcellulose, hydroxyethylcellulose, polyethylene glycol, carboxyvinyl polymer, polyacrylate, polyacrylamide, polyvinyl alcohol, polyvinylpyrrolidone, polyvinyl acetate saponified, xanthan gum, guar gum, sodium alginate, Gum arabic, agar, gelatin, pectin, dextrin, starch, lignin sulfonate, vinyl acetate, isobutylmaleic acid copolymer, carboxylate, aluminum magnesium silicate, magnesium silicate, bentonite, montmorillonite, attapulgite, sepiolite, etc. can be used. . As the solvent, other than water, alcohols such as methanol, ethanol, isopropanol, normal propanol, isobutanol, ethylene glycol and propylene glycol, ketones such as acetone, methyl ethyl ketone, methyl propyl ketone, methyl butyl ketone and dipropyl ketone, Ethyl acetate, propyl acetate, isopropyl acetate,
Esters such as butyl acetate, amyl acetate, ethyl butyrate,
Hydrocarbons such as n-hexane, cyclohexane, heptane, etc., petroleum such as kerosene, white spirit, mineral spirit, naphtha, diethylene glycol, ethylene glycol alkyl ether, diethylene glycol alkyl ether, oligoethylene glycol alkyl ether, dipropylene glycol, propylene glycol Glycol solvents such as alkyl ethers, dipropylene glycol alkyl ethers, oligopropylene glycol alkyl ethers, and glycerin can be used. As the solubilizing agent, paratoluenesulfonic acid, sodium sulfosuccinate and the like can be used.
【0011】残留シリコ−ン上をプライマ−により被覆
する工程に使用するプライマ−としては、アクリルシリ
コン系プライマ−、変性シリコ−ン系プライマ−、ポリ
エステル系プライマ−等が好適に利用できる。As the primer used in the step of coating the residual silicone with the primer, an acrylic silicon-based primer, a modified silicone-based primer, a polyester-based primer and the like can be suitably used.
【0012】残留シリコ−ン表面に紫外線を照射する工
程に使用する紫外線光源としては、例えば、水銀灯、キ
セノンランプ、殺菌灯等が利用できる。As the ultraviolet light source used in the step of irradiating the surface of the residual silicon with ultraviolet light, for example, a mercury lamp, a xenon lamp, a germicidal lamp and the like can be used.
【0013】光触媒性親水性コ−ティング液は、光触媒
粒子を必須構成要素とする。その他に、常温から150
゜程度の低温で基材に固着させるための熱硬化性樹脂、
紫外線硬化性樹脂、湿分硬化性樹脂の前駆体を添加する
こともできる。ここで樹脂には耐光触媒酸化性や耐光性
の観点からシリコン樹脂を用いるのが好ましい。その他
にコ−ティング液には、溶媒、界面活性剤、重合硬化触
媒、加水分解触媒、レベリング剤、抗菌金属、pH調整
剤、保存安定剤などが添加されていてもよい。The photocatalytic hydrophilic coating liquid contains photocatalyst particles as an essential component. In addition, from room temperature to 150
熱 Thermosetting resin for fixing to base material at low temperature,
A precursor of an ultraviolet curable resin or a moisture curable resin can also be added. Here, it is preferable to use a silicone resin as the resin from the viewpoint of light catalytic oxidation resistance and light resistance. In addition, a solvent, a surfactant, a polymerization curing catalyst, a hydrolysis catalyst, a leveling agent, an antibacterial metal, a pH adjuster, a storage stabilizer, and the like may be added to the coating liquid.
【0014】本発明において、光触媒とは、その結晶の
伝導帯と価電子帯との間のエネルギ−ギャップよりも大
きなエネルギ−(すなわち短い波長)の光(励起光)を
照射したときに、価電子帯中の電子の励起(光励起)が
生じて、伝導電子と正孔を生成しうる物質をいい、光触
媒性酸化物には、例えば、アナタ−ゼ型酸化チタン、ル
チル型酸化チタン、酸化亜鉛、酸化錫、酸化第二鉄、三
酸化二ビスマス、三酸化タングステン、チタン酸ストロ
ンチウム等の酸化物が好適に利用できる。In the present invention, a photocatalyst is a catalyst that emits light (excitation light) having a larger energy (ie, shorter wavelength) than the energy gap between the conduction band and the valence band of the crystal. A substance capable of generating conduction electrons and holes by excitation of electrons (photoexcitation) in the electron band. Photocatalytic oxides include, for example, anatase-type titanium oxide, rutile-type titanium oxide, and zinc oxide Oxides such as tin oxide, ferric oxide, bismuth trioxide, tungsten trioxide and strontium titanate can be suitably used.
【0015】請求項19の(a)に記述されるシリケ−
トは、平均組成式SiXqO(4-q)/2(式中、Xはアルコ
キシ基、又は、ハロゲン原子であり、qは0<q<4を
満足する数である)で表されるシリケ−トからなる塗膜
形成要素である。この樹脂は後述する無定型シリカの前
駆体を部分的に加水分解、脱水縮重合することにより得
ることができる。A silicate according to claim 19 (a).
Is represented by an average composition formula SiX q O (4-q) / 2 (where X is an alkoxy group or a halogen atom, and q is a number satisfying 0 <q <4). This is a coating film forming element made of silicate. This resin can be obtained by partially hydrolyzing and dehydrating and condensing a precursor of amorphous silica described below.
【0016】ここで無定型シリカの前駆体としては、平
均組成式SiXqO(4-q)/2(式中、Xはアルコキシ基、
又は、ハロゲン原子であり、qは0<q<4を満足する
数である)で表されるシリケ−トからなる塗膜形成要
素、又は一般式SiX4(式中、Xはアルコキシ基、又
は、ハロゲン原子である)で表される4官能加水分解性
シラン誘導体からなる塗膜形成要素等が好適に利用でき
る。Here, the precursor of the amorphous silica includes an average composition formula SiX q O (4-q) / 2 (where X is an alkoxy group,
Or a halogen atom, q is 0 <q <silicate represented by 4 is a number satisfying) - film former consisting of bets, or the general formula SiX 4 (wherein, X is an alkoxy group, or , A halogen atom) can be suitably used.
【0017】ここで上記4官能加水分解性シラン誘導体
からなる塗膜形成要素としては、テトラメトキシシラ
ン、テトラエトキシシラン、テトラプロポキシシラン、
テトラブトキシシラン、ジエトキシジメトキシシラン等
が好適に利用できる。Here, as the coating film forming element comprising the above-mentioned tetrafunctional hydrolyzable silane derivative, tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane,
Tetrabutoxysilane, diethoxydimethoxysilane and the like can be suitably used.
【0018】また、上記シリケ−トからなる塗膜形成要
素としては、上記4官能加水分解性シラン誘導体の部分
加水分解及び脱水縮重合等で作製することができる。Further, the coating film forming element comprising the above silicate can be prepared by partial hydrolysis, dehydration condensation polymerization, etc. of the above-mentioned tetrafunctional hydrolyzable silane derivative.
【0019】請求項20の(a)に記述されるシリコ−
ンは、平均組成式RpSiO(4-p)/2(式中、Rは一価の
有機基の1種若しくは2種以上からなる官能基、又は、
一価の有機基と水素基から選ばれた2種以上からなる官
能基であり、Xはアルコキシ基、又は、ハロゲン原子で
あり、pは0<p<2を満足する数である)で表される
樹脂である。この樹脂は後述するシリコ−ンの前駆体を
部分的に加水分解、脱水縮重合することにより得ること
ができる。The silicone described in claim 20 (a)
Is an average compositional formula R p SiO (4-p) / 2 (where R is a functional group comprising one or more monovalent organic groups, or
X is an alkoxy group or a halogen atom, and p is a number satisfying 0 <p <2). It is a resin that is used. This resin can be obtained by partially hydrolyzing and dehydrating polycondensation of a silicone precursor described later.
【0020】ここでシリコ−ンの前駆体としては、平均
組成式RpSiXqO(4-p-q)/2(式中、Rは一価の有機
基の1種若しくは2種以上からなる官能基、又は、一価
の有機基と水素基から選ばれた2種以上からなる官能基
であり、Xはアルコキシ基、又は、ハロゲン原子であ
り、p及びqは0<p<2、0<q<4を満足する数で
ある)で表されるシロキサンからなる塗膜形成要素、又
は一般式RpSiX4-p(式中、Rは一価の有機基の1種
若しくは2種以上からなる官能基、又は、一価の有機基
と水素基から選ばれた2種以上からなる官能基であり、
Xはアルコキシ基、又は、ハロゲン原子であり、pは1
または2である)で表される加水分解性シラン誘導体か
らなる塗膜形成要素、が好適に利用できる。Here, the precursor of the silicone is an average compositional formula R p SiX q O (4-pq) / 2 (where R is a functional group comprising one or more monovalent organic groups) X or a functional group composed of two or more selected from a monovalent organic group and a hydrogen group, X is an alkoxy group or a halogen atom, and p and q are 0 <p <2, 0 < a film-forming element composed of a siloxane represented by the following formula: q <4, or a general formula R p SiX 4-p (wherein R represents one or more monovalent organic groups) Or a functional group consisting of two or more selected from a monovalent organic group and a hydrogen group,
X is an alkoxy group or a halogen atom, and p is 1
Or 2), which is preferably composed of a hydrolyzable silane derivative represented by the formula (1).
【0021】ここで上記加水分解性シラン誘導体からな
る塗膜形成要素としては、メチルトリメトキシシラン、
メチルトリエトキシシラン、メチルトリプロポキシシラ
ン、メチルトリブトキシシラン、エチルトリメトキシシ
ラン、エチルトリエトキシシラン、エチルトリプロポキ
シシラン、エチルトリブトキシシラン、フェニルトリメ
トキシシラン、フェニルトリエトキシシラン、フェニル
トリプロポキシシラン、フェニルトリブトキシシラン、
ジメチルジメトキシシラン、ジメチルジエトキシシラ
ン、ジメチルジプロポキシシラン、ジメチルジブトキシ
シラン、ジエチルジメトキシシラン、ジエチルジエトキ
シシラン、ジエチルジプロポキシシラン、ジエチルジブ
トキシシラン、フェニルメチルジメトキシシラン、フェ
ニルメチルジエトキシシラン、フェニルメチルジプロポ
キシシラン、フェニルメチルジブトキシシラン、n−プ
ロピルトリメトキシシラン、n−プロピルトリエトキシ
シラン、n−プロピルトリプロポキシシラン、n−プロ
ピルトリブトキシシラン、γ−グリコキシドキシプロピ
ルトリメトキシシラン、γ−アクリロキシプロピルトリ
メトキシシラン等が好適に利用できる。Here, as the coating film forming element comprising the hydrolyzable silane derivative, methyltrimethoxysilane,
Methyltriethoxysilane, methyltripropoxysilane, methyltributoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, ethyltripropoxysilane, ethyltributoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, phenyltripropoxysilane, Phenyltributoxysilane,
Dimethyldimethoxysilane, dimethyldiethoxysilane, dimethyldipropoxysilane, dimethyldibutoxysilane, diethyldimethoxysilane, diethyldiethoxysilane, diethyldipropoxysilane, diethyldibutoxysilane, phenylmethyldimethoxysilane, phenylmethyldiethoxysilane, phenyl Methyldipropoxysilane, phenylmethyldibutoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, n-propyltripropoxysilane, n-propyltributoxysilane, γ-glycoxydoxypropyltrimethoxysilane, γ -Acryloxypropyltrimethoxysilane and the like can be suitably used.
【0022】また、上記シロキサンからなる塗膜形成要
素としては、上記加水分解性シラン誘導体の部分加水分
解及び脱水縮重合、又は上記加水分解性シラン誘導体の
部分加水分解物と、テトラメトキシシラン、テトラエト
キシシラン、テトラプロポキシシラン、テトラブトキシ
シラン、ジエトキシジメトキシシラン等の部分加水分解
物との脱水縮重合等で作製することができる。The film-forming element composed of the siloxane includes partial hydrolysis and dehydration-condensation polymerization of the hydrolyzable silane derivative, or partial hydrolyzate of the hydrolyzable silane derivative, tetramethoxysilane and tetramethoxysilane. It can be produced by dehydration condensation polymerization with a partial hydrolyzate such as ethoxysilane, tetrapropoxysilane, tetrabutoxysilane, diethoxydimethoxysilane and the like.
【0023】本発明で使用する溶媒には、水、アルコ−
ル等が利用できる。特に、分子量60〜300の液状ア
ルコ−ルが好ましい。それにより、塗膜形成時に溶媒中
の分子量60以上(沸点80℃以上)の液状アルコ−ル
の蒸発が適度に遅いために、コ−ティング組成物を塗布
する際に、コ−ティング組成物の分散性の溶媒蒸発を原
因とする変動を抑制することができるので、透明かつ均
一な塗膜を形成することが可能となる。分子量60〜3
00の液状アルコ−ルとしては、例えば、n−プロパノ
−ル、イソプロパノ−ル、t−ブタノ−ル、イソブタノ
−ル、n−ブタノ−ル、2−メチルプロパノ−ル、ペン
タノ−ル、エチレングリコ−ル、モノアセトンアルコ−
ル、ジアセトンアルコ−ル、エチレングリコ−ルモノメ
チルエ−テル、4−ヒドロキシ−4−メチル−2−ペン
タノン、ジプロピレングリコ−ル、プロピレングリコ−
ル、トリプロピレングリコ−ル、1−エトキシ−2−プ
ロパノ−ル、1−ブトキシ−2−プロパノ−ル、1−プ
ロポキシ−2−プロパノ−ル、プロピレングリコ−ルモ
ノメチルエ−テル、ジプロピレングリコ−ルモノメチル
エ−テル、ジプロピレングリコ−ルモノエチルエ−テ
ル、トリプロピレングリコ−ルモノメチルエ−テル等が
好適に利用できる。The solvent used in the present invention includes water, alcohol
Can be used. Particularly, a liquid alcohol having a molecular weight of 60 to 300 is preferable. As a result, the evaporation of the liquid alcohol having a molecular weight of 60 or more (boiling point of 80 ° C. or more) in the solvent during formation of the coating film is moderately slow, so that when the coating composition is applied, Since fluctuations due to dispersible solvent evaporation can be suppressed, a transparent and uniform coating film can be formed. Molecular weight 60-3
Examples of the liquid alcohol of No. 00 include n-propanol, isopropanol, t-butanol, isobutanol, n-butanol, 2-methylpropanol, pentanole and ethylene glycol. , Monoacetone alcohol
Alcohol, diacetone alcohol, ethylene glycol monomethyl ether, 4-hydroxy-4-methyl-2-pentanone, dipropylene glycol, propylene glycol
, Tripropylene glycol, 1-ethoxy-2-propanol, 1-butoxy-2-propanol, 1-propoxy-2-propanol, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether -Tel, dipropylene glycol monoethyl ether, tripropylene glycol monomethyl ether and the like can be suitably used.
【0024】重合触媒としては、アルミニウムキレ−
ト、アルミニウムアセチルアセトナ−ト、過塩素酸アル
ミニウム、塩化アルミニウム、アルミニウムイソブトキ
シド、アルミニウムイソプロポキシドのようなアルミニ
ウム化合物;テトライソプロピルチタネ−ト、テトラブ
トキシチタネ−トのようなチタン化合物;水酸化ナトリ
ウム、水酸化リチウム、水酸化カリウム、ナトリウムメ
チラ−ト、酢酸ナトリウム、ギ酸ナトリウム、酢酸カリ
ウム、ギ酸カリウム、プロピオン酸カリウム、テトラメ
チルアンモニウムヒドロキシドのような塩基性化合物
類;n−ヘキシルアミン、トリブチルアミン、ジアザビ
シクロウンデセン、エチレンジアミン、ヘキサンジアミ
ン、ジエチレントリアミン、テトラエチレンベンタミ
ン、トリエチレンテトラミン、エタノ−ルアミン類、γ
−アミノプロピルトリメトキシシラン、γ−アミノプロ
ピルメチルジメトキシシラン、γ−(2−アミノメチ
ル)−アミノプロピルトリメトキシシラン、γ−(2−
アミノメチル)−アミノプロピルメチルジメトキシシラ
ンのようなアミン化合物;錫アセチルアセトナ−ト、ジ
ブチル錫オクチレ−トのような錫化合物;コバルトオク
チレ−ト、コバルトアセチルアセトナ−ト、鉄アセチル
アセトナ−トのような金属化合物類;リン酸、硝酸、フ
タル酸、p−トルエンスルホン酸、トリクロル酢酸のよ
うな酸性化合物類などが挙げられる。As the polymerization catalyst, aluminum chelate is used.
Aluminum compounds such as aluminum, aluminum acetylacetonate, aluminum perchlorate, aluminum chloride, aluminum isobutoxide, aluminum isopropoxide; titanium compounds such as tetraisopropyl titanate and tetrabutoxy titanate; Basic compounds such as sodium hydroxide, lithium hydroxide, potassium hydroxide, sodium methylate, sodium acetate, sodium formate, potassium acetate, potassium formate, potassium propionate, and tetramethylammonium hydroxide; n-hexyl Amine, tributylamine, diazabicycloundecene, ethylenediamine, hexanediamine, diethylenetriamine, tetraethylenebentamine, triethylenetetramine, ethanolamines, γ
-Aminopropyltrimethoxysilane, γ-aminopropylmethyldimethoxysilane, γ- (2-aminomethyl) -aminopropyltrimethoxysilane, γ- (2-
Amine compounds such as aminomethyl) -aminopropylmethyldimethoxysilane; tin compounds such as tin acetylacetonate and dibutyltin octylate; cobalt octylate, cobalt acetylacetonate, and iron acetylacetonate Metal compounds such as phosphoric acid, nitric acid, phthalic acid, p-toluenesulfonic acid, and acidic compounds such as trichloroacetic acid.
【0025】加水分解触媒としては、pH2〜5の硝
酸、塩酸、酢酸、硫酸、スルホン酸、マレイン酸、プロ
ピオン酸、アジピン酸、フマル酸、フタル酸、吉草酸、
乳酸、酪酸、クエン酸、リンゴ酸、ピクリン酸、ギ酸、
炭酸、フェノ−ル等が好適に利用できる。As the hydrolysis catalyst, nitric acid, hydrochloric acid, acetic acid, sulfuric acid, sulfonic acid, maleic acid, propionic acid, adipic acid, fumaric acid, phthalic acid, valeric acid having a pH of 2 to 5,
Lactic acid, butyric acid, citric acid, malic acid, picric acid, formic acid,
Carbonic acid, phenol and the like can be suitably used.
【0026】レベリング剤としては、ジアセトンアルコ
−ル、エチレングリコ−ルモノメチルエ−テル、4−ヒ
ドロキシ−4−メチル−2−ペンタノン、ジプロピレン
グリコ−ル、トリプロピレングリコ−ル、1−エトキシ
−2−プロパノ−ル、1−ブトキシ−2−プロパノ−
ル、プロピレングリコ−ルモノメチルエ−テル、1−プ
ロポキシ−2−プロパノ−ル、ジプロピレングリコ−ル
モノメチルエ−テル、ジプロピレングリコ−ルモノエチ
ルエ−テル、トリプロピレングリコ−ルモノエチルエ−
テル等が好適に利用できる。Examples of the leveling agent include diacetone alcohol, ethylene glycol monomethyl ether, 4-hydroxy-4-methyl-2-pentanone, dipropylene glycol, tripropylene glycol and 1-ethoxy-2. -Propanol, 1-butoxy-2-propano-
Propylene glycol monomethyl ether, 1-propoxy-2-propanol, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, tripropylene glycol monoethyl ether.
Tels and the like can be suitably used.
【0027】抗菌金属としては、Ag、Cu、Znのよ
うな金属を添加することができる。前記金属を添加した
場合、塗膜により形成される表面層は、表面に付着した
細菌や黴を暗所でも死滅させることができる。As the antibacterial metal, metals such as Ag, Cu and Zn can be added. When the metal is added, the surface layer formed by the coating film can kill bacteria and fungi attached to the surface even in a dark place.
【0028】コ−ティング組成物には、Pt、Pd、R
u、Rh、Ir、Osのような白金族金属を添加するこ
とができる。前記金属を添加した場合、塗膜により形成
される表面層は、光触媒の酸化還元活性を増強でき、有
機物汚れの分解性、有害気体や悪臭の分解性を向上させ
ることができる。The coating composition includes Pt, Pd, R
A platinum group metal such as u, Rh, Ir, Os can be added. When the metal is added, the surface layer formed by the coating film can enhance the oxidation-reduction activity of the photocatalyst, and can improve the decomposability of organic contaminants and harmful gases and odors.
【0029】コ−ティング組成物には、前記に記載した
ような界面活性剤を添加することができる。前記界面活
性剤を添加することによって基材表面への濡れ性を向上
させることができる。The above-mentioned surfactants can be added to the coating composition. The wettability to the substrate surface can be improved by adding the surfactant.
【0030】本発明のコ−ティング組成物の利用方法
は、基本的には、基材表面にコ−ティング組成物を塗布
し、硬化させて塗膜を形成することによる。The method of using the coating composition of the present invention is basically based on applying the coating composition to the surface of a substrate and curing the coating composition to form a coating film.
【0031】上記コ−ティング組成物の塗布方法として
は、スプレ−コ−ティング法、ディップコ−ティング
法、フロ−コ−ティング法、スピンコ−ティング法、ロ
−ルコ−ティング法、刷毛塗り、スポンジ塗り等の方法
が好適に利用できる。硬化方法としては、熱処理、室温
放置、紫外線照射等により重合させて行うことができ
る。The coating method of the above coating composition includes spray coating, dip coating, flow coating, spin coating, roll coating, brush coating, and sponge. A method such as coating can be suitably used. As a curing method, it can be carried out by polymerizing by heat treatment, standing at room temperature, ultraviolet irradiation, or the like.
【0032】上記方法で部材表面に塗膜を形成すると、
部材表面は光触媒の光励起に応じて親水性を呈するよう
になる。ここで、光触媒の光励起により、基材表面が高
度に親水化されるためには、励起光の照度は0.001
mW/cm2以上あればよいが、0.01mW/cm2以
上だと好ましく、0.1mW/cm2以上だとより好ま
しい。光触媒性酸化物が、アナタ−ゼ型酸化チタン、ル
チル型酸化チタン、酸化亜鉛、チタン酸ストロンチウム
の場合には、光触媒の光励起に用いる光源としては、太
陽光、室内照明、蛍光灯、水銀灯、白熱電灯、キセノン
ランプ、高圧ナトリウムランプ、メタルハライドラン
プ、BLBランプ等が好適に利用できる。 また、光触
媒性酸化物が酸化錫の場合には、殺菌灯、BLBランプ
等が好適に利用できる。When a coating film is formed on the member surface by the above method,
The surface of the member becomes hydrophilic in response to the photoexcitation of the photocatalyst. Here, in order for the substrate surface to be highly hydrophilized by photoexcitation of the photocatalyst, the illuminance of the excitation light must be 0.001.
mW suffices / cm 2 or more, but preferably that it 0.01 mW / cm 2 or more, and more preferably it 0.1 mW / cm 2 or more. When the photocatalytic oxide is an anatase type titanium oxide, a rutile type titanium oxide, a zinc oxide, or a strontium titanate, the light source used for photoexcitation of the photocatalyst is sunlight, indoor lighting, fluorescent lamp, mercury lamp, incandescent lamp. Electric lamps, xenon lamps, high-pressure sodium lamps, metal halide lamps, BLB lamps and the like can be suitably used. When the photocatalytic oxide is tin oxide, a germicidal lamp, a BLB lamp, or the like can be suitably used.
【0033】部材表面に塗膜により形成される表面層の
膜厚は、0.4μm以下にするのが好ましい。そうすれ
ば、光の乱反射による白濁を防止することができ、表面
層は実質的に透明となる。さらに、表面層の膜厚を、
0.2μm以下にすると一層好ましい。そうすれば、光
の干渉による表面層の発色を防止することができる。ま
た、表面層が薄ければ薄いほどその透明度は向上する。
更に、膜厚を薄くすれば、表面層の耐摩耗性が向上す
る。The thickness of the surface layer formed by a coating film on the member surface is preferably 0.4 μm or less. Then, cloudiness due to irregular reflection of light can be prevented, and the surface layer becomes substantially transparent. Furthermore, the thickness of the surface layer is
It is more preferable that the thickness be 0.2 μm or less. Then, it is possible to prevent the surface layer from being colored by light interference. Also, the thinner the surface layer, the better its transparency.
Further, when the film thickness is reduced, the wear resistance of the surface layer is improved.
【0034】PCT/WO96/29375号に示した
ように、基材表面が水との接触角に換算して10゜以下
の状態であれば、空気中の湿分や湯気が結露しても、凝
縮水が個々の水滴を形成せずに一様な水膜になる傾向が
顕著になる。従って、表面に光散乱性の曇りを生じない
傾向が顕著になる。同様に、窓ガラスや車両用バックミ
ラ−や車両用風防ガラスや眼鏡レンズやヘルメットのシ
−ルドが降雨や水しぶきを浴びた場合に、離散した目障
りな水滴が形成されずに、高度の視界と可視性を確保
し、車両や交通の安全性を保証し、種々の作業や活動の
能率を向上させる効果が飛躍的に向上する。また、同様
にPCT/WO96/29375号に示したように、基
材表面が水との接触角に換算して20゜以下の状態であ
れば、都市煤塵、自動車等の排気ガスに含有されるカ−
ボンブラック等の燃焼生成物、油脂、シ−ラント溶出成
分等の疎水性汚染物質、及び無機粘土質汚染物質双方が
付着しにくく、付着しても降雨や水洗により簡単に落せ
る状態になる。As shown in PCT / WO96 / 29375, if the surface of the base material is not more than 10 ° in terms of the contact angle with water, even if moisture or steam in the air is dewed, The tendency of condensed water to form a uniform water film without forming individual water droplets becomes remarkable. Therefore, the tendency that light scattering fogging does not occur on the surface becomes remarkable. Similarly, when a window glass, a vehicle back mirror, a vehicle windshield, an eyeglass lens, or a shield of a helmet is exposed to rainfall or splashing, discrete unsightly water droplets are not formed, and high visibility and visibility are achieved. As a result, the effects of ensuring vehicle safety, ensuring the safety of vehicles and traffic, and improving the efficiency of various tasks and activities are dramatically improved. Similarly, as shown in PCT / WO96 / 29375, when the surface of the base material is in a state of not more than 20 ° in terms of a contact angle with water, it is contained in exhaust gas from city dust, automobiles, and the like. Car
Both combustion products such as bon black, hydrophobic contaminants such as oils and fats, sealant eluting components, and inorganic clay contaminants do not easily adhere, and even if they adhere, they can be easily dropped by rainfall or washing with water.
【0035】基材表面が上記高度の親水性を呈し、かつ
その状態を維持するようになれば、上記防曇効果、表面
清浄化効果の他、帯電防止効果(ほこり付着防止効
果)、断熱効果、水中での気泡付着防止効果、熱交換器
における効率向上効果、生体親和性向上効果等が発揮さ
れるようになる。If the surface of the base material exhibits the above-mentioned high hydrophilicity and maintains the state, the anti-fogging effect, the surface cleaning effect, the antistatic effect (dust adhesion preventing effect), and the heat insulating effect. Thus, an effect of preventing air bubbles from adhering in water, an effect of improving efficiency in a heat exchanger, an effect of improving biocompatibility, and the like are exhibited.
【0036】本発明が適用可能な基材としては、防曇効
果を期待する場合には透明な基材であり、その材質はガ
ラス、プラスチック等が好適に利用できる。適用可能な
基材を用途でいえば、車両用後方確認ミラ−、浴室用
鏡、洗面所用鏡、歯科用鏡、道路鏡のような鏡;眼鏡レ
ンズ、光学レンズ、照明用レンズ、半導体用レンズ、複
写機用レンズ、車両用後方確認カメラレンズのようなレ
ンズ;プリズム;建物や監視塔の窓ガラス;自動車、鉄
道車両、航空機、船舶、潜水艇、雪上車、ロ−プウエイ
のゴンドラ、遊園地のゴンドラ、宇宙船のような乗物の
窓ガラス;自動車、オ−トバイ、鉄道車両、航空機、船
舶、潜水艇、雪上車、スノ−モ−ビル、ロ−プウエイの
ゴンドラ、遊園地のゴンドラ、宇宙船のような乗物の風
防ガラス;防護用ゴ−グル、スポ−ツ用ゴ−グル、防護
用マスクのシ−ルド、スポ−ツ用マスクのシ−ルド、ヘ
ルメットのシ−ルド、冷凍食品陳列ケ−スのガラス、中
華饅頭等の保温食品の陳列ケ−スのガラス;計測機器の
カバ−、車両用後方確認カメラレンズのカバ−、レ−ザ
−歯科治療器等の集束レンズ、車間距離センサ−等のレ
−ザ−光検知用センサ−のカバ−、赤外線センサ−のカ
バ−;カメラ用フィルタ−、及び上記物品表面に貼着さ
せるためのフィルム、シ−ト、シ−ル等を含む。The substrate to which the present invention can be applied is a transparent substrate when an anti-fogging effect is expected, and glass, plastic, and the like can be suitably used as the material. Speaking of applicable base materials, mirrors such as rearview mirrors for vehicles, mirrors for bathrooms, mirrors for toilets, dental mirrors, road mirrors; spectacle lenses, optical lenses, illumination lenses, semiconductor lenses Lenses such as copier lenses, rear view camera lenses for vehicles; prisms; windows of buildings and towers; automobiles, railway vehicles, aircraft, ships, submersibles, snowmobiles, lowway gondola, amusement parks Gondolas, vehicle windows such as spaceships; cars, motorbikes, railcars, aircraft, ships, submersibles, snowmobiles, snowmobiles, lowway gondola, amusement park gondola, space Windshield for vehicles such as ships; protective goggles, sports goggles, protective mask shield, sports mask shield, helmet shield, frozen food display Case glass, Chinese bun, etc. Glass for display case of warm food; Cover for measuring equipment, Cover for rear view camera lens for vehicle, Focusing lens for laser dental treatment device, etc., Laser light detection for inter-vehicle distance sensor, etc. Cover for an infrared sensor, a cover for an infrared sensor, a filter for a camera, and a film, a sheet, a seal, and the like to be attached to the surface of the article.
【0037】本発明が適用可能な基材としては、表面清
浄化効果を期待する場合にはその材質は、例えば、金
属、セラミック、ガラス、プラスチック、木、石、セメ
ント、コンクリ−ト、繊維、布帛、それらの組合せ、そ
れらの積層体が好適に利用できる。適用可能な基材を用
途でいえば、建材、建物外装、建物内装、窓枠、窓ガラ
ス、構造部材、乗物の外装及び塗装、機械装置や物品の
外装、防塵カバ−及び塗装、交通標識、各種表示装置、
広告塔、道路用遮音壁、鉄道用遮音壁、橋梁、ガ−ドレ
−ルの外装及び塗装、トンネル内装及び塗装、碍子、太
陽電池カバ−、太陽熱温水器集熱カバ−、ビニ−ルハウ
ス、車両用照明灯のカバ−、住宅設備、便器、浴槽、洗
面台、照明器具、照明カバ−、台所用品、食器、食器洗
浄器、食器乾燥器、流し、調理レンジ、キッチンフ−
ド、換気扇、及び上記物品表面に貼着させるためのフィ
ルム、シ−ト、シ−ル等を含む。When a surface cleaning effect is expected as a substrate to which the present invention can be applied, the material may be, for example, metal, ceramic, glass, plastic, wood, stone, cement, concrete, fiber, or the like. Fabrics, combinations thereof, and laminates thereof can be suitably used. Speaking of applicable base materials, building materials, building exteriors, building interiors, window frames, windowpanes, structural members, vehicle exteriors and coatings, machinery and articles exteriors, dustproof covers and coatings, traffic signs, Various display devices,
Advertising towers, noise barriers for roads, noise barriers for railways, bridges, exterior and coating of garages, tunnel interiors and coatings, insulators, solar battery covers, solar water heater collector covers, vinyl houses, vehicle lighting Light covers, housing equipment, toilets, bathtubs, washbasins, lighting fixtures, lighting covers, kitchen utensils, dishes, dishwashers, dish dryers, sinks, cooking ranges, kitchen hoods
And a film, a sheet, a seal, and the like for attaching to the surface of the article.
【0038】本発明が適用可能な基材としては、乾燥促
進効果を期待する場合にはその材質は、例えば、金属、
セラミック、ガラス、プラスチック、木、石、セメン
ト、コンクリ−ト、繊維、布帛、それらの組合せ、それ
らの積層体が好適に利用できる。適用可能な基材を用途
でいえば、自動車車体、窓、舗道及び上記物品表面に貼
着させるためのフィルム、シ−ト、シ−ル等を含む。As a substrate to which the present invention can be applied, when a drying acceleration effect is expected, its material is, for example, metal,
Ceramic, glass, plastic, wood, stone, cement, concrete, fiber, fabric, combinations thereof, and laminates thereof can be suitably used. Examples of applicable substrates include automobile bodies, windows, pavements, and films, sheets, seals, and the like to be adhered to the surface of the article.
【0039】本発明が適用可能な基材としては、帯電防
止効果を期待する場合にはその材質は、例えば、金属、
セラミック、ガラス、プラスチック、木、石、セメン
ト、コンクリ−ト、繊維、布帛、それらの組合せ、それ
らの積層体が好適に利用できる。適用可能な基材を用途
でいえば、ブラウン管、磁気記録メディア、光記録メデ
ィア、光磁気記録メディア、オ−ディオテ−プ、ビデオ
テ−プ、アナログレコ−ド、家庭用電気製品のハウジン
グや部品や外装及び塗装、OA機器製品のハウジングや
部品や外装及び塗装、建材、建物外装、建物内装、窓
枠、窓ガラス、構造部材、乗物の外装及び塗装、機械装
置や物品の外装、防塵カバ−及び塗装、及び上記物品表
面に貼着させるためのフィルム、シ−ト、シ−ル等を含
む。As a substrate to which the present invention can be applied, when an antistatic effect is expected, its material is, for example, metal,
Ceramic, glass, plastic, wood, stone, cement, concrete, fiber, fabric, combinations thereof, and laminates thereof can be suitably used. Speaking of applicable substrates, cathode ray tubes, magnetic recording media, optical recording media, magneto-optical recording media, audio tapes, video tapes, analog records, housings and parts for household electrical appliances, Exterior and painting, OA equipment product housing and parts and exterior and painting, building materials, building exterior, building interior, window frames, window glass, structural members, vehicle exterior and painting, mechanical equipment and articles exterior, dustproof cover and Includes films, sheets, seals, etc. for painting and sticking to the surface of the article.
【0040】[0040]
実施例1〜9;窓ガラスへの適用 実施例1.北側に面した窓の塗布面周辺を、塗料の周辺
への飛散を防止するためにマスキングした後、界面活性
剤としてアルキルベンゼンスルホン酸ナトリウム及び脂
肪酸アルカノ−ルアミドが添加されている水系洗浄剤
(pH9.5)を含浸させたウエスで窓を拭いて付着汚
れを除去した。次いで、水を含浸させたウエスで窓を拭
いて洗浄剤を除去し、さらにワイパ−及び乾いたウエス
にて窓に付着する水分を除去した。次いで、石原産業製
光触媒コ−ティング液ST−K01(酸化チタン粒子8
重量部とアルキルシリケ−ト2重量部と硝酸水溶液5
4.8重量部とメタノ−ル28重量部とプロパノ−ル
7.2重量部からなる組成物)と、石原産業製光触媒コ
−ティング液ST−K03(酸化チタン粒子5重量部と
アルキルシリケ−ト5重量部と硝酸水溶液54.8重量
部とメタノ−ル28重量部とプロパノ−ル7.2重量部
からなる組成物)を1対1で混合して得た液を2−プロ
パノ−ルで25倍希釈して得た光触媒コ−ティング液A
を、上記洗浄処理を施した窓ガラス表面にφ0.8mm
のエアガンを用いて105g/m2スプレ−コ−ティン
グ法により塗布後、20℃で20分乾燥させることによ
り、塗膜を硬化させて、#1試料を得た。一方、比較の
ため、上記洗浄処理を施していない北側に面した窓にも
上記光触媒コ−ティング液Aを同様にスプレ−コ−ティ
ング法により塗布後、20℃で20分乾燥させることに
より、塗膜を硬化させて、#2試料を得た。次に、#1
試料、#2試料について水との接触角及び外観を調べ
た。水との接触角は窓ガラス試料を、塗膜形成後、2日
放置して太陽光に晒すことにより、紫外線が照射される
ようにし、その後、取り外した窓ガラスについて、水と
の接触角を接触角測定器(協和界面科学,CA−X15
0)を用い、マイクロシリンジから試料表面に水滴を滴
下30秒後に測定することにより調べた。その結果、#
2試料では水との接触角は30゜程度であったのに対
し、#1試料では水との接触角は0゜まで超親水化され
た。また、#2試料表面はやや白濁する様子が見られた
のに対し、#1試料は透明であった。Examples 1 to 9; application to window glass. After masking the periphery of the application surface of the window facing the north side to prevent the paint from scattering around the periphery, a water-based detergent (pH 9.5) to which sodium alkylbenzenesulfonate and fatty acid alkanolamide are added as surfactants. The window was wiped with a cloth impregnated with 5) to remove adhered dirt. Next, the window was wiped with a water-impregnated rag to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Next, a photocatalyst coating solution ST-K01 (Titanium oxide particles 8
Parts by weight, 2 parts by weight of alkyl silicate and aqueous solution of nitric acid 5
A composition consisting of 4.8 parts by weight, 28 parts by weight of methanol and 7.2 parts by weight of propanol) and a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles and alkyl silicate) 5 parts by weight, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol) are mixed in a one-to-one ratio, and the solution obtained is mixed with 2-propanol. Photocatalyst coating liquid A obtained by diluting 25-fold
On the surface of the window glass that has been subjected to the above-mentioned cleaning treatment, φ0.8 mm
Co - - of 105 g / m 2 spray with air gun after coating by plating method, by drying 20 minutes at 20 ° C., to cure the coating film to obtain # 1 specimen. On the other hand, for comparison, the above-mentioned photocatalyst coating liquid A was also applied to the window facing the north side not subjected to the above-mentioned cleaning treatment by the spray coating method, and then dried at 20 ° C. for 20 minutes. The coating was cured to give a # 2 sample. Next, # 1
The contact angle with water and the appearance of the sample # 2 were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. Contact angle measuring instrument (Kyowa Interface Science, CA-X15
Using 0), water droplets were dropped on the sample surface from the microsyringe and measured 30 seconds later. as a result,#
In the two samples, the contact angle with water was about 30 °, whereas in the # 1 sample, the contact angle with water was superhydrophilized to 0 °. The # 2 sample surface was slightly turbid, while the # 1 sample was transparent.
【0041】実施例2.北側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、ノニオン系界面活性剤とアルカリ無機ビルダ−が
添加されている水系洗浄剤(pH11.9)を含浸させ
たウエスで窓を拭いて付着汚れを除去した。次いで、水
を含浸させたウエスで窓を拭いて洗浄剤を除去し、さら
にワイパ−及び乾いたウエスにて窓に付着する水分を除
去した。次いで、石原産業製光触媒コ−ティング液ST
−K01(酸化チタン粒子8重量部とアルキルシリケ−
ト2重量部と硝酸水溶液54.8重量部とメタノ−ル2
8重量部とプロパノ−ル7.2重量部からなる組成物)
と、石原産業製光触媒コ−ティング液ST−K03(酸
化チタン粒子5重量部とアルキルシリケ−ト5重量部と
硝酸水溶液54.8重量部とメタノ−ル28重量部とプ
ロパノ−ル7.2重量部からなる組成物)を1対1で混
合して得た液を2−プロパノ−ルで25倍希釈して得た
光触媒コ−ティング液Aを、上記洗浄処理を施した窓ガ
ラス表面にφ0.8mmのエアガンを用いて105g/
m2スプレ−コ−ティング法により塗布後、20℃で2
0分乾燥させることにより、塗膜を硬化させて、#3試
料を得た。 次に、#3試料について水との接触角及び
外観を調べた。 水との接触角は窓ガラス試料を、塗膜
形成後、2日放置して太陽光に晒すことにより、紫外線
が照射されるようにし、その後、取り外した窓ガラスに
ついて、水との接触角を測定した。その結果、水との接
触角は0゜まで超親水化された。また、試料は透明であ
った。Embodiment 2 FIG. After masking the area around the application surface of the window facing the north side to prevent the paint from scattering around the area, a water-based detergent (pH 11.9) containing a nonionic surfactant and an alkali-inorganic builder is added. The window was wiped with an impregnated rag to remove adhered dirt. Next, the window was wiped with a water-impregnated rag to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Next, a photocatalyst coating solution ST manufactured by Ishihara Sangyo
-K01 (8 parts by weight of titanium oxide particles and alkyl silicate)
2 parts by weight, 54.8 parts by weight of an aqueous nitric acid solution and methanol 2
Composition comprising 8 parts by weight and 7.2 parts by weight of propanol)
And a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Of a photocatalyst coating liquid A obtained by diluting a liquid obtained by mixing the composition consisting of 1: 1) and 2-propanol 25-fold, onto the surface of the window glass having been subjected to the above-mentioned washing treatment. 105g / using a 0.8mm air gun
After coating by m 2 spray coating method,
The coating film was cured by drying for 0 minutes to obtain a # 3 sample. Next, the contact angle with water and the appearance of the # 3 sample were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. It was measured. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0042】実施例3.北側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、ノニオン系界面活性剤とレベリング剤が添加され
ている石油及び水を溶媒とする洗浄剤(pH6.9)を
含浸させたウエスで窓を拭いて付着汚れを除去した。次
いで、水を含浸させたウエスで窓を拭いて洗浄剤を除去
し、さらにワイパ−及び乾いたウエスにて窓に付着する
水分を除去した。次いで、石原産業製光触媒コ−ティン
グ液ST−K01(酸化チタン粒子8重量部とアルキル
シリケ−ト2重量部と硝酸水溶液54.8重量部とメタ
ノ−ル28重量部とプロパノ−ル7.2重量部からなる
組成物)と、石原産業製光触媒コ−ティング液ST−K
03(酸化チタン粒子5重量部とアルキルシリケ−ト5
重量部と硝酸水溶液54.8重量部とメタノ−ル28重
量部とプロパノ−ル7.2重量部からなる組成物)を1
対1で混合して得た液を2−プロパノ−ルで25倍希釈
して得た光触媒コ−ティング液Aを、上記洗浄処理を施
した窓ガラス表面にφ0.8mmのエアガンを用いて1
05g/m2スプレ−コ−ティング法により塗布後、2
0℃で20分乾燥させることにより、塗膜を硬化させ
て、#4試料を得た。次に、#4試料について水との接
触角及び外観を調べた。水との接触角は窓ガラス試料
を、塗膜形成後、2日放置して太陽光に晒すことによ
り、紫外線が照射されるようにし、その後、取り外した
窓ガラスについて、水との接触角を測定した。その結
果、水との接触角は0゜まで超親水化された。また、試
料は透明であった。Embodiment 3 FIG. After masking the area around the application surface of the window facing the north side in order to prevent the paint from scattering around the area, a cleaning agent (pH 6) containing petroleum and water to which a nonionic surfactant and a leveling agent are added is used. The window was wiped with a rag impregnated with .9) to remove adhered dirt. Next, the window was wiped with a water-impregnated rag to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) A photocatalyst coating liquid ST-K manufactured by Ishihara Sangyo Co., Ltd.)
03 (5 parts by weight of titanium oxide particles and alkyl silicate 5
1 part by weight of a nitric acid aqueous solution, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol.
The photocatalyst coating liquid A obtained by diluting the liquid obtained by mixing one to one with 2-propanol was applied to the surface of the window glass having been subjected to the above-mentioned washing treatment by using an air gun of φ0.8 mm.
After coating by a spray coating method of 05 g / m 2 , 2
The coating was cured by drying at 0 ° C. for 20 minutes to obtain a # 4 sample. Next, the contact angle with water and the appearance of the # 4 sample were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. It was measured. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0043】実施例4.北側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、ノニオン系界面活性剤とアニオン系界面活性剤が
添加されている水系洗浄剤(pH7.9)を含浸させた
ウエスで窓を拭いて付着汚れを除去した。次いで、水を
含浸させたウエスで窓を拭いて洗浄剤を除去し、さらに
ワイパ−及び乾いたウエスにて窓に付着する水分を除去
した。次いで、石原産業製光触媒コ−ティング液ST−
K01(酸化チタン粒子8重量部とアルキルシリケ−ト
2重量部と硝酸水溶液54.8重量部とメタノ−ル28
重量部とプロパノ−ル7.2重量部からなる組成物)
と、石原産業製光触媒コ−ティング液ST−K03(酸
化チタン粒子5重量部とアルキルシリケ−ト5重量部と
硝酸水溶液54.8重量部とメタノ−ル28重量部とプ
ロパノ−ル7.2重量部からなる組成物)を1対1で混
合して得た液を2−プロパノ−ルで25倍希釈して得た
光触媒コ−ティング液Aを、上記洗浄処理を施した窓ガ
ラス表面にφ0.8mmのエアガンを用いて105g/
m2スプレ−コ−ティング法により塗布後、20℃で2
0分乾燥させることにより、塗膜を硬化させて、#5試
料を得た。次に、#5試料について水との接触角及び外
観を調べた。水との接触角は窓ガラス試料を、塗膜形成
後、2日放置して太陽光に晒すことにより、紫外線が照
射されるようにし、その後、取り外した窓ガラスについ
て、水との接触角を測定した。その結果、水との接触角
は0゜まで超親水化された。また、試料は透明であっ
た。Embodiment 4 FIG. A water-based detergent (pH 7.9) to which a nonionic surfactant and an anionic surfactant are added after masking the area around the application surface of the window facing the north side to prevent the paint from scattering around the area. The window was wiped with a rag impregnated with, to remove adhered dirt. Next, the window was wiped with a water-impregnated rag to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Next, photocatalyst coating solution ST-
K01 (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of aqueous nitric acid solution, and methanol 28
(A composition comprising parts by weight and 7.2 parts by weight of propanol)
And a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Of a photocatalyst coating liquid A obtained by diluting a liquid obtained by mixing the composition consisting of 1: 1) and 2-propanol 25-fold, onto the surface of the window glass having been subjected to the above-mentioned washing treatment. 105g / using a 0.8mm air gun
After coating by m 2 spray coating method,
The coating film was cured by drying for 0 minutes to obtain a # 5 sample. Next, the contact angle with water and the appearance of the # 5 sample were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. It was measured. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0044】実施例5.西側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、ノニオン系界面活性剤とアミンが添加されている
水系洗浄剤(pH11.8)を含浸させたウエスで窓を
拭いて付着汚れを除去した。次いで、水を含浸させたウ
エスで窓を拭いて洗浄剤を除去し、さらにワイパ−及び
乾いたウエスにて窓に付着する水分を除去した。次い
で、石原産業製光触媒コ−ティング液ST−K01(酸
化チタン粒子8重量部とアルキルシリケ−ト2重量部と
硝酸水溶液54.8重量部とメタノ−ル28重量部とプ
ロパノ−ル7.2重量部からなる組成物)と、石原産業
製光触媒コ−ティング液ST−K03(酸化チタン粒子
5重量部とアルキルシリケ−ト5重量部と硝酸水溶液5
4.8重量部とメタノ−ル28重量部とプロパノ−ル
7.2重量部からなる組成物)を1対1で混合して得た
液を2−プロパノ−ルで25倍希釈して得た光触媒コ−
ティング液Aを、上記洗浄処理を施した窓ガラス表面に
φ0.8mmのエアガンを用いて105g/m2スプレ
−コ−ティング法により塗布後、20℃で20分乾燥さ
せることにより、塗膜を硬化させて、#6試料を得た。
次に、#6試料について水との接触角及び外観を調べ
た。水との接触角は窓ガラス試料を、塗膜形成後、2日
放置して太陽光に晒すことにより、紫外線が照射される
ようにし、その後、取り外した窓ガラスについて、水と
の接触角を測定した。 その結果、水との接触角は0゜
まで超親水化された。また、試料は透明であった。Embodiment 5 FIG. The area around the application surface of the window facing the west was masked to prevent the paint from scattering around, and then impregnated with an aqueous detergent (pH 11.8) containing a nonionic surfactant and an amine. The window was wiped with a rag to remove the adhered dirt. Next, the window was wiped with a water-impregnated rag to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Parts) and a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate and 5 parts by weight of nitric acid aqueous solution).
A liquid obtained by mixing 4.8 parts by weight, 28 parts by weight of methanol and 7.2 parts by weight of propanol) in a one-to-one ratio is diluted 25-fold with 2-propanol to obtain a liquid. Photocatalyst core
The coating liquid A was applied to the surface of the window glass subjected to the above-mentioned cleaning treatment by a spray coating method of 105 g / m 2 using an air gun of φ0.8 mm, and then dried at 20 ° C. for 20 minutes to form a coating film. After curing, a # 6 sample was obtained.
Next, the contact angle with water and the appearance of the # 6 sample were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. It was measured. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0045】実施例6.西側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、電解アルカリ水を成分とする洗浄剤(ペイントハ
ウス製、ハングリーウォーター)を含浸させたウエスで
窓を拭いて付着汚れを除去した。次いで、水を含浸させ
たウエスで窓を拭いて洗浄剤を除去し、さらにワイパ−
及び乾いたウエスにて窓に付着する水分を除去した。次
いで、石原産業製光触媒コ−ティング液ST−K01
(酸化チタン粒子8重量部とアルキルシリケ−ト2重量
部と硝酸水溶液54.8重量部とメタノ−ル28重量部
とプロパノ−ル7.2重量部からなる組成物)と、石原
産業製光触媒コ−ティング液ST−K03(酸化チタン
粒子5重量部とアルキルシリケ−ト5重量部と硝酸水溶
液54.8重量部とメタノ−ル28重量部とプロパノ−
ル7.2重量部からなる組成物)を1対1で混合して得
た液を2−プロパノ−ルで25倍希釈して得た光触媒コ
−ティング液Aを、上記洗浄処理を施した窓ガラス表面
にφ0.8mmのエアガンを用いて105g/m2スプ
レ−コ−ティング法により塗布後、20℃で20分乾燥
させることにより、塗膜を硬化させて、#7試料を得
た。次に、#7試料について水との接触角及び外観を調
べた。水との接触角は窓ガラス試料を、塗膜形成後、2
日放置して太陽光に晒すことにより、紫外線が照射され
るようにし、その後、取り外した窓ガラスについて、水
との接触角を測定した。その結果、水との接触角は0゜
まで超親水化された。また、試料は透明であった。Embodiment 6 FIG. After masking the area around the application surface of the window facing the west to prevent the paint from scattering around the area, use a cloth impregnated with a detergent (Hungry Water, manufactured by Paint House) containing electrolytic alkaline water as a component. Was wiped off to remove adhered dirt. Next, the window was wiped with a rag impregnated with water to remove the cleaning agent, and further wiped.
Then, water adhering to the window was removed with a dry waste cloth. Next, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo Co., Ltd.
(A composition comprising 8 parts by weight of titanium oxide particles, 2 parts by weight of an alkyl silicate, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol); -Sting liquid ST-K03 (5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and propanol-
Of a photocatalyst coating liquid A obtained by diluting a liquid obtained by mixing 1: 1 of a composition consisting of 7.2 parts by weight of toluene with 2-propanol and subjecting it to the above-mentioned washing treatment. After coating on the surface of the window glass by a spray coating method of 105 g / m 2 using an air gun of φ0.8 mm, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 7 sample. Next, the contact angle with water and the appearance of the # 7 sample were examined. The contact angle with water was determined by measuring the window glass sample after coating film formation.
By leaving it for a day and exposing it to sunlight, ultraviolet rays were irradiated. Thereafter, the contact angle with water was measured for the removed window glass. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0046】実施例7.西側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、酸化セリウム研磨剤が添加されている洗浄剤を含
浸させたウエスで窓を拭いて付着汚れを除去した。次い
で、水を含浸させたウエスで窓を拭いて洗浄剤を除去
し、さらにワイパ−及び乾いたウエスにて窓に付着する
水分を除去した。次いで、石原産業製光触媒コ−ティン
グ液ST−K01(酸化チタン粒子8重量部とアルキル
シリケ−ト2重量部と硝酸水溶液54.8重量部とメタ
ノ−ル28重量部とプロパノ−ル7.2重量部からなる
組成物)と、石原産業製光触媒コ−ティング液ST−K
03(酸化チタン粒子5重量部とアルキルシリケ−ト5
重量部と硝酸水溶液54.8重量部とメタノ−ル28重
量部とプロパノ−ル7.2重量部からなる組成物)を1
対1で混合して得た液を2−プロパノ−ルで25倍希釈
して得た光触媒コ−ティング液Aを、上記洗浄処理を施
した窓ガラス表面にφ0.8mmのエアガンを用いて1
05g/m2スプレ−コ−ティング法により塗布後、2
0℃で20分乾燥させることにより、塗膜を硬化させ
て、#8試料を得た。次に、#8試料について水との接
触角及び外観を調べた。水との接触角は窓ガラス試料
を、塗膜形成後、2日放置して太陽光に晒すことによ
り、紫外線が照射されるようにし、その後、取り外した
窓ガラスについて、水との接触角を測定した。その結
果、水との接触角は0゜まで超親水化された。また、試
料は透明であった。Embodiment 7 FIG. After masking the area around the application surface of the window facing the west to prevent the paint from scattering around the area, wipe the window with a cloth impregnated with a cleaning agent containing cerium oxide abrasive to remove any adhered dirt. Removed. Next, the window was wiped with a water-impregnated rag to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) A photocatalyst coating liquid ST-K manufactured by Ishihara Sangyo Co., Ltd.)
03 (5 parts by weight of titanium oxide particles and alkyl silicate 5
1 part by weight of a nitric acid aqueous solution, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol.
The photocatalyst coating liquid A obtained by diluting the liquid obtained by mixing one to one with 2-propanol was applied to the surface of the window glass having been subjected to the above-mentioned washing treatment by using an air gun of φ0.8 mm.
After coating by a spray coating method of 05 g / m 2 , 2
The coating was cured by drying at 0 ° C. for 20 minutes to obtain a # 8 sample. Next, the contact angle with water and the appearance of the # 8 sample were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. It was measured. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0047】実施例8.西側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、水を含浸させたウエスで窓を拭いた後、n−ヘキ
サンを含浸させたウエスで窓を拭いて付着汚れを除去し
た。さらに、乾いたウエスにて窓に付着する溶剤を除去
した。次いで、石原産業製光触媒コ−ティング液ST−
K01(酸化チタン粒子8重量部とアルキルシリケ−ト
2重量部と硝酸水溶液54.8重量部とメタノ−ル28
重量部とプロパノ−ル7.2重量部からなる組成物)
と、石原産業製光触媒コ−ティング液ST−K03(酸
化チタン粒子5重量部とアルキルシリケ−ト5重量部と
硝酸水溶液54.8重量部とメタノ−ル28重量部とプ
ロパノ−ル7.2重量部からなる組成物)を1対1で混
合して得た液を2−プロパノ−ルで25倍希釈して得た
光触媒コ−ティング液Aを、上記洗浄処理を施した窓ガ
ラス表面にφ0.8mmのエアガンを用いて105g/
m2スプレ−コ−ティング法により塗布後、20℃で2
0分乾燥させることにより、塗膜を硬化させて、#9試
料を得た。次に、#9試料について水との接触角及び外
観を調べた。水との接触角は窓ガラス試料を、塗膜形成
後、2日放置して太陽光に晒すことにより、紫外線が照
射されるようにし、その後、取り外した窓ガラスについ
て、水との接触角を測定した。その結果、水との接触角
は0゜まで超親水化された。また、試料は透明であっ
た。Embodiment 8 FIG. After masking the area around the application surface of the window facing the west to prevent the paint from scattering around, the window was wiped with a water-impregnated cloth, and then the window was cleaned with n-hexane-impregnated cloth. It was wiped to remove the adhered dirt. Further, the solvent adhering to the window was removed with a dry rag. Next, photocatalyst coating solution ST-
K01 (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of aqueous nitric acid solution, and methanol 28
(A composition comprising parts by weight and 7.2 parts by weight of propanol)
And a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Of a photocatalyst coating liquid A obtained by diluting a liquid obtained by mixing the composition consisting of 1: 1) and 2-propanol 25-fold, onto the surface of the window glass having been subjected to the above-mentioned washing treatment. 105g / using a 0.8mm air gun
After coating by m 2 spray coating method,
The coating film was cured by drying for 0 minutes to obtain a # 9 sample. Next, the contact angle with water and the appearance of the # 9 sample were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. It was measured. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0048】実施例9.西側に面した窓の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、塩基性シリカゾル、モノエタノールアミン、ノニ
オン性界面活性剤、グリコール系溶媒、エタノール、お
よび水からなる洗浄剤を含浸させたウエスで窓を拭いて
付着汚れを除去した。次いで、石原産業製光触媒コ−テ
ィング液ST−K01(酸化チタン粒子8重量部とアル
キルシリケ−ト2重量部と硝酸水溶液54.8重量部と
メタノ−ル28重量部とプロパノ−ル7.2重量部から
なる組成物)を1−プロパノ−ル、レベリング剤からな
る混合溶媒(1−プロパノール90重量部、プロピレン
グリコールエチルエーテル10重量部)で50倍希釈し
て得た光触媒コ−ティング液を、上記洗浄処理を施した
窓ガラス表面にポリプロピレン製不織布により塗布後、
20℃で20分乾燥させることにより、塗膜を硬化させ
て、#10試料を得た。次に、#10試料について水と
の接触角及び外観を調べた。水との接触角は窓ガラス試
料を、塗膜形成後、2日放置して太陽光に晒すことによ
り、紫外線が照射されるようにし、その後、取り外した
窓ガラスについて、水との接触角を測定した。その結
果、水との接触角は0゜まで超親水化された。また、試
料は透明であった。Embodiment 9 FIG. After masking the area around the application surface of the window facing the west to prevent the paint from scattering around, it consists of basic silica sol, monoethanolamine, nonionic surfactant, glycol solvent, ethanol, and water The window was wiped with a rag impregnated with a cleaning agent to remove adhered dirt. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Of a photocatalyst coating liquid obtained by diluting a 1-propanol and a leveling agent with a mixed solvent (90 parts by weight of 1-propanol and 10 parts by weight of propylene glycol ethyl ether) 50-fold. After coating with a polypropylene non-woven fabric on the window glass surface that has been subjected to the above-mentioned cleaning treatment,
The coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 10 sample. Next, the contact angle with water and the appearance of the # 10 sample were examined. The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. It was measured. As a result, the contact angle with water was superhydrophilized to 0 °. Also, the sample was transparent.
【0049】実施例10〜12;永久汚れが付着した窓
ガラスへの適用 実施例10.北側に面した空調機の室外機の噴出口近く
に設置された窓の塗布面周辺を、塗料の周辺への飛散を
防止するためにマスキングした後、酸性弗化アンモニウ
ムが添加されている洗浄剤を含浸させたウエスで、有色
付着汚れ及びカルシウム塩付着汚れを除去した。次い
で、水道水で洗い流した後、水を含浸させたウエスで窓
を拭いて洗浄剤を除去し、さらにワイパ−及び乾いたウ
エスにて窓に付着する水分を除去した。次いで、石原産
業製光触媒コ−ティング液ST−K01(酸化チタン粒
子8重量部とエチルシリケ−ト2重量部と硝酸水溶液5
4.8重量部とメタノ−ル28重量部とプロパノ−ル
7.2重量部からなる組成物)と石原産業製光触媒コ−
ティング液ST−K03(酸化チタン粒子5重量部とエ
チルシリケ−ト5重量部と硝酸水溶液54.8重量部と
メタノ−ル28重量部とプロパノ−ル7.2重量部から
なる組成物)を1:1で混合した液を2−プロパノ−ル
で25倍希釈して得た光触媒性コ−ティング液Aを、上
記洗浄処理を施した窓ガラス表面にφ0.8mmのエア
ガンを用いて105g/m2スプレ−コ−ティング法に
より塗布後、20℃で20分乾燥させることにより、塗
膜を硬化させて、#11試料を得た。一方、比較のた
め、上記洗浄処理を施していない北側に面した窓にも上
記光触媒性コ−ティング液Aを同様にスプレ−コ−ティ
ング法により塗布後、20℃で20分乾燥させることに
より、塗膜を硬化させて、#12試料を得た。次に、#
11試料、#12試料について水との接触角及び外観を
調べた。水との接触角は窓ガラス試料を、塗膜形成後、
2日放置して太陽光に晒すことにより、紫外線が照射さ
れるようにし、その後、取り外した窓ガラスについて、
水との接触角を接触角測定器(協和界面科学、CA−X
150)を用い、マイクロシリンジから試料表面に水滴
を滴下30秒後に測定することにより調べた。その結
果、#11試料、#12試料共に0゜まで超親水化され
た。但し、その外観は、#12試料では白色汚れが認め
られたのに対し、#11試料では透明性を維持した。Examples 10 to 12; Application to window glass with permanent stains A cleaning agent containing ammonium acid fluoride after masking the area around the application surface of the window installed near the outlet of the outdoor unit of the air conditioner facing the north to prevent the paint from scattering around The colored stain and the calcium salt stain were removed with a cloth impregnated with. Next, after washing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, moisture adhering to the window was removed with a wiper and a dry rag. Next, a photocatalyst coating liquid ST-K01 (Itahara Sangyo Co., Ltd.) (8 parts by weight of titanium oxide particles, 2 parts by weight of ethyl silicate, and 5 parts of nitric acid aqueous solution)
A composition comprising 4.8 parts by weight, 28 parts by weight of methanol and 7.2 parts by weight of propanol) and a photocatalyst core manufactured by Ishihara Sangyo Co., Ltd.
1 part of the liquid ST-K03 (a composition comprising 5 parts by weight of titanium oxide particles, 5 parts by weight of ethyl silicate, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol). : 1. The liquid mixed at 1: 1 was diluted 25-fold with 2-propanol, and the photocatalytic coating liquid A was applied to the window glass surface having been subjected to the above-mentioned cleaning treatment to 105 g / m 2 using a φ0.8 mm air gun. (2) After coating by a spray coating method, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 11 sample. On the other hand, for comparison, the above-mentioned photocatalytic coating liquid A was also applied to the window facing the north side not subjected to the above-mentioned cleaning treatment by the spray coating method, and then dried at 20 ° C. for 20 minutes. Then, the coating film was cured to obtain a # 12 sample. next,#
Eleven samples and # 12 samples were examined for contact angles with water and appearance. The contact angle with water was measured for the window glass sample after coating film formation.
By leaving it for two days and exposing it to sunlight, the ultraviolet rays are radiated.
A contact angle measuring device for measuring the contact angle with water (Kyowa Interface Science, CA-X
150), a water drop was dropped on the sample surface from the microsyringe and measured 30 seconds after the drop. As a result, both the # 11 sample and the # 12 sample were superhydrophilized to 0 °. However, as for the appearance, the white stain was observed in the # 12 sample, while the transparency was maintained in the # 11 sample.
【0050】実施例11.北側に面した空調機の室外機
の噴出口近くに設置された窓の塗布面周辺を、塗料の周
辺への飛散を防止するためにマスキングした後、酸化セ
リウム研磨剤が添加されている洗浄剤を含浸させたウエ
スで、有色付着汚れ及びカルシウム塩付着汚れを除去し
た。次いで、水道水で洗い流した後、水を含浸させたウ
エスで窓を拭いて洗浄剤を除去し、さらにワイパ−及び
乾いたウエスにて窓に付着する水分を除去した。次い
で、石原産業製光触媒コ−ティング液ST−K01(酸
化チタン粒子8重量部とエチルシリケ−ト2重量部と硝
酸水溶液54.8重量部とメタノ−ル28重量部とプロ
パノ−ル7.2重量部からなる組成物)と石原産業製光
触媒コ−ティング液ST−K03(酸化チタン粒子5重
量部とエチルシリケ−ト5重量部と硝酸水溶液54.8
重量部とメタノ−ル28重量部とプロパノ−ル7.2重
量部からなる組成物)を1:1で混合した液を2−プロ
パノ−ルで25倍希釈して得た光触媒性コ−ティング液
Aを、上記洗浄処理を施した窓ガラス表面にφ0.8m
mのエアガンを用いて105g/m2スプレ−コ−ティ
ング法により塗布後、20℃で20分乾燥させることに
より、塗膜を硬化させて、#13試料を得た。#13試
料について水との接触角及び外観を調べた。その結果、
0゜まで超親水化された。また、その外観も透明性を維
持した。Embodiment 11 FIG. Cleaning agent to which the cerium oxide abrasive is added after masking the area around the application surface of the window installed near the outlet of the outdoor unit of the air conditioner facing the north to prevent the paint from scattering around The colored stain and the calcium salt stain were removed with a cloth impregnated with. Next, after washing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, moisture adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating liquid ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of ethyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Parts) and a photocatalyst coating solution ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles, 5 parts by weight of ethyl silicate, and 54.8 parts of nitric acid aqueous solution).
Photocatalytic coating obtained by diluting a liquid obtained by mixing 1: 1 by weight of a composition consisting of 28 parts by weight of methanol, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) with 2-propanol 25-fold. The solution A was applied to the surface of the window glass having been subjected to the above-mentioned cleaning treatment by φ0.8 m.
After coating by a spray coating method of 105 g / m 2 using an air gun of m, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 13 sample. The contact angle with water and the appearance of the # 13 sample were examined. as a result,
It was superhydrophilized to 0 °. In addition, its appearance maintained transparency.
【0051】実施例12.北側に面した空調機の室外機
の噴出口近くに設置された窓の塗布面周辺を、塗料の周
辺への飛散を防止するためにマスキングした後、ケイ酸
系鉱物からなる研磨剤が添加されている洗浄剤(東陶機
器、TOTOパウダ−)を含浸させたウエスで、有色付
着汚れ及びカルシウム塩付着汚れを除去した。次いで、
水道水で洗い流した後、水を含浸させたウエスで窓を拭
いて洗浄剤を除去し、さらにワイパ−及び乾いたウエス
にて窓に付着する水分を除去した。次いで、石原産業製
光触媒コ−ティング液ST−K01(酸化チタン粒子8
重量部とエチルシリケ−ト2重量部と硝酸水溶液54.
8重量部とメタノ−ル28重量部とプロパノ−ル7.2
重量部からなる組成物)と石原産業製光触媒コ−ティン
グ液ST−K03(酸化チタン粒子5重量部とエチルシ
リケ−ト5重量部と硝酸水溶液54.8重量部とメタノ
−ル28重量部とプロパノ−ル7.2重量部からなる組
成物)を1:1で混合した液を2−プロパノ−ルで25
倍希釈して得た光触媒性コ−ティング液Aを、上記洗浄
処理を施した窓ガラス表面にφ0.8mmのエアガンを
用いて105g/m2スプレ−コ−ティング法により塗
布後、20℃で20分乾燥させることにより、塗膜を硬
化させて、#14試料を得た。#14試料について水と
の接触角及び外観を調べた。その結果、0゜まで超親水
化された。また、その外観も透明性を維持した。Embodiment 12 FIG. After masking the area around the application surface of the window installed near the outlet of the outdoor unit of the air conditioner facing the north side to prevent the paint from scattering around, an abrasive made of silicate mineral was added. A stain impregnated with the used cleaning agent (TOTO KIKI, TOTO powder) was used to remove stains stained with color and calcium salt. Then
After rinsing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Next, a photocatalyst coating solution ST-K01 (Titanium oxide particles 8
54 parts by weight, 2 parts by weight of ethyl silicate and an aqueous solution of nitric acid
8 parts by weight, 28 parts by weight of methanol and 7.2 parts of propanol
Parts by weight) and a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles, 5 parts by weight of ethyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and propanol Of a mixture consisting of 7.2 parts by weight of 2-propanol in 2-propanol.
The photocatalytic coating solution A obtained by doubling the dilution was applied to the surface of the window glass having been subjected to the above-mentioned cleaning treatment by a spray coating method of 105 g / m 2 using an air gun of φ0.8 mm. The coating film was cured by drying for 20 minutes to obtain a # 14 sample. The contact angle with water and the appearance of the # 14 sample were examined. As a result, it became superhydrophilic to 0 °. In addition, its appearance maintained transparency.
【0052】実施例13〜16;シリコーンシーリング
剤に起因する汚れが付着した窓ガラスへの適用 実施例13.北側に面したシリコ−ンシ−ラントの下部
に設置された窓の塗布面周辺を、塗料の周辺への飛散を
防止するためにマスキングした後、酸性弗化アンモニウ
ムが添加されている洗浄剤を含浸させたウエスで、有色
付着汚れ及びシ−ラント付着汚れを除去した。次いで、
水道水で洗い流した後、水を含浸させたウエスで窓を拭
いて洗浄剤を除去し、さらにワイパ−及び乾いたウエス
にて窓に付着する水分を除去した。次いで、石原産業製
光触媒コ−ティング液ST−K01(酸化チタン粒子8
重量部とアルキルシリケ−ト2重量部と硝酸水溶液5
4.8重量部とメタノ−ル28重量部とプロパノ−ル
7.2重量部からなる組成物)と石原産業製光触媒コ−
ティング液ST−K03(酸化チタン粒子5重量部とア
ルキルシリケ−ト5重量部と硝酸水溶液54.8重量部
とメタノ−ル28重量部とプロパノ−ル7.2重量部か
らなる組成物)を1:1で混合した液を2−プロパノ−
ルで25倍希釈して得た光触媒コ−ティング液Aを、上
記洗浄処理を施した窓ガラス表面にφ0.8mmのエア
ガンを用いて105g/m2スプレ−コ−ティング法に
より塗布後、20℃で20分乾燥させることにより、塗
膜を硬化させて、#15試料を得た。一方、比較のた
め、上記洗浄処理を施していない北側に面した窓にも上
記光触媒コ−ティング液Aを同様にスプレ−コ−ティン
グ法により塗布しようと試みたが、コ−ティング液が基
材表面になじまずに弾いてしまい、均一な塗膜形成がで
きなかった。その後、20℃で20分乾燥させることに
より、塗膜を硬化させて、#16試料を得た。次に、#
15試料、#16試料について水との接触角を調べた。
水との接触角は窓ガラス試料を、塗膜形成後、2日放置
して太陽光に晒すことにより、紫外線が照射されるよう
にし、その後、取り外した窓ガラスについて、水との接
触角を接触角測定器(協和界面科学、CA−X150)
を用い、マイクロシリンジから試料表面に水滴を滴下3
0秒後に測定することにより調べた。その結果、#16
試料では水との接触角は80゜であったのに対し、#1
5試料では水との接触角は0゜まで超親水化された。Examples 13 to 16; Application to window glass to which dirt caused by a silicone sealant adhered. After masking the area around the application surface of the window installed below the silicone sealant facing the north side to prevent the paint from scattering around, impregnated with a detergent containing ammonium acid fluoride The stained stain and the stain stained with the sealant were removed from the waste cloth. Then
After rinsing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Next, a photocatalyst coating solution ST-K01 (Titanium oxide particles 8
Parts by weight, 2 parts by weight of alkyl silicate and aqueous solution of nitric acid 5
A composition comprising 4.8 parts by weight, 28 parts by weight of methanol and 7.2 parts by weight of propanol) and a photocatalyst core manufactured by Ishihara Sangyo Co., Ltd.
1 part of a liquid ST-K03 (a composition comprising 5 parts by weight of titanium oxide particles, 5 parts by weight of an alkyl silicate, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol). : 2-propano-
After coating the photocatalyst coating solution A obtained by diluting 25 times with a nozzle with a spray coating method of 105 g / m 2 using an air gun of φ0.8 mm on the surface of the window glass having been subjected to the above-mentioned washing treatment, the coating solution was applied. The coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 15 sample. On the other hand, for comparison, an attempt was made to apply the photocatalyst coating liquid A to the window facing the north side, which had not been subjected to the cleaning treatment, by the spray coating method. The material was repelled without being adapted to the material surface, and a uniform coating film could not be formed. Thereafter, the coating was cured by drying at 20 ° C. for 20 minutes to obtain a # 16 sample. next,#
The contact angle with water was examined for 15 samples and # 16 sample.
The contact angle with water was determined by exposing the window glass sample to ultraviolet light by leaving it for 2 days after forming the coating film and exposing it to sunlight. Contact angle measuring instrument (Kyowa Interface Science, CA-X150)
Drop a water droplet on the sample surface from the micro syringe using
It was determined by measuring after 0 seconds. As a result, # 16
In the sample, the contact angle with water was 80 °, while the contact angle with water was # 1.
In five samples, the contact angle with water was superhydrophilized to 0 °.
【0053】実施例14.北側に面したシリコ−ンシ−
ラントの下部に設置された窓の塗布面周辺を、塗料の周
辺への飛散を防止するためにマスキングした後、酸化セ
リウム研磨剤が添加されている洗浄剤を含浸させたウエ
スで拭い、有色付着汚れ及びシ−ラント付着汚れを除去
した。次いで、水道水で洗い流した後、水を含浸させた
ウエスで窓を拭いて洗浄剤を除去し、さらにワイパ−及
び乾いたウエスにて窓に付着する水分を除去した。次い
で、石原産業製光触媒コ−ティング液ST−K01(酸
化チタン粒子8重量部とアルキルシリケ−ト2重量部と
硝酸水溶液54.8重量部とメタノ−ル28重量部とプ
ロパノ−ル7.2重量部からなる組成物)と石原産業製
光触媒コ−ティング液ST−K03(酸化チタン粒子5
重量部とアルキルシリケ−ト5重量部と硝酸水溶液5
4.8重量部とメタノ−ル28重量部とプロパノ−ル
7.2重量部からなる組成物)を1:1で混合した液を
2−プロパノ−ルで25倍希釈して得た光触媒コ−ティ
ング液Aを、上記洗浄処理を施した窓ガラス表面にφ
0.8mmのエアガンを用いて105g/m2スプレ−
コ−ティング法により塗布後、20℃で20分乾燥させ
ることにより、塗膜を硬化させて、#17試料を得た。
次に、#17試料について水との接触角を調べた。その
結果、水との接触角は0゜まで超親水化された。Embodiment 14 FIG. Silicone facing north
After masking the area around the application surface of the window installed at the bottom of the runt to prevent the paint from scattering around, wipe with a cloth impregnated with a cleaning agent containing cerium oxide abrasive, and apply color. Dirt and sealant-adhered dirt were removed. Next, after washing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, moisture adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Parts) and a photocatalyst coating liquid ST-K03 (titanium oxide particles 5) manufactured by Ishihara Sangyo Co., Ltd.
Parts by weight, 5 parts by weight of alkyl silicate and 5 parts of nitric acid aqueous solution
A composition comprising 4.8 parts by weight, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) was mixed at a ratio of 1: 1 to obtain a photocatalyst core obtained by diluting 25-fold with 2-propanol. -Plating liquid A is applied to the surface of the window glass which has been subjected to the above-mentioned cleaning treatment by φ.
105 g / m 2 spray using a 0.8 mm air gun
After coating by a coating method, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 17 sample.
Next, the contact angle with water was examined for the # 17 sample. As a result, the contact angle with water was superhydrophilized to 0 °.
【0054】実施例15.北側に面したシリコ−ンシ−
ラントの下部に設置された窓の塗布面周辺を、塗料の周
辺への飛散を防止するためにマスキングした後、酸化セ
リウム研磨剤が添加されている洗浄剤を含浸させたウエ
スで窓を拭いた後、乾いたウエスで洗浄剤を除去した。
次いで、電解アルカリ水を成分とする洗浄剤(ペイント
ハウス製、ハングリーウォーター)を含浸させたウエス
で窓を拭き、水を含浸させたウエスで洗浄剤を除去し、
さらにワイパ−及び乾いたウエスにて窓に付着する水分
を除去した。次いで、石原産業製光触媒コ−ティング液
ST−K01(酸化チタン粒子8重量部とアルキルシリ
ケ−ト2重量部と硝酸水溶液54.8重量部とメタノ−
ル28重量部とプロパノ−ル7.2重量部からなる組成
物)と石原産業製光触媒コ−ティング液ST−K03
(酸化チタン粒子5重量部とアルキルシリケ−ト5重量
部と硝酸水溶液54.8重量部とメタノ−ル28重量部
とプロパノ−ル7.2重量部からなる組成物)を1:1
で混合した液を2−プロパノ−ルで25倍希釈して得た
光触媒コ−ティング液Aを、上記洗浄処理を施した窓ガ
ラス表面にφ0.8mmのエアガンを用いて105g/
m2スプレ−コ−ティング法により塗布後、20℃で2
0分乾燥させることにより、塗膜を硬化させて、#18
試料を得た。次に、#18試料について水との接触角を
調べた。その結果、水との接触角は0゜まで超親水化さ
れた。Embodiment 15 FIG. Silicone facing north
After masking the area around the application surface of the window installed at the lower part of the runt to prevent the paint from scattering around, the window was wiped with a cloth impregnated with a cleaning agent to which cerium oxide abrasive was added. Thereafter, the cleaning agent was removed with a dry rag.
Next, the window was wiped with a rag impregnated with a detergent containing electrolytic alkaline water (Hungry Water, manufactured by Paint House), and the detergent was removed with a rag impregnated with water.
Further, water adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, and methanol
Composition consisting of 28 parts by weight of toluene and 7.2 parts by weight of propanol) and a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo.
(A composition comprising 5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) is 1: 1.
The solution mixed in the above was diluted 25-fold with 2-propanol, and the photocatalyst coating solution A obtained was applied to the window glass surface having been subjected to the above-mentioned washing treatment at a rate of 105 g / cm 2 using an air gun of φ0.8 mm.
After coating by m 2 spray coating method,
By drying for 0 minutes, the coating film is hardened, and # 18
A sample was obtained. Next, the contact angle with water was examined for the # 18 sample. As a result, the contact angle with water was superhydrophilized to 0 °.
【0055】実施例16.北側に面したシリコ−ンシ−
ラントの下部に設置された窓の塗布面周辺を、塗料の周
辺への飛散を防止するためにマスキングした後、けい酸
系鉱物からなる研磨剤が添加されている洗浄剤(東陶機
器、TOTOパウダー)を含浸させたウエスで拭い、有色付
着汚れ及びシ−ラント付着汚れを除去した。次いで、水
道水で洗い流した後、水を含浸させたウエスで窓を拭い
て洗浄剤を除去し、さらにワイパ−及び乾いたウエスに
て窓に付着する水分を除去した。次いで、石原産業製光
触媒コ−ティング液ST−K01(酸化チタン粒子8重
量部とアルキルシリケ−ト2重量部と硝酸水溶液54.
8重量部とメタノ−ル28重量部とプロパノ−ル7.2
重量部からなる組成物)と石原産業製光触媒コ−ティン
グ液ST−K03(酸化チタン粒子5重量部とアルキル
シリケ−ト5重量部と硝酸水溶液54.8重量部とメタ
ノ−ル28重量部とプロパノ−ル7.2重量部からなる
組成物)を1:1で混合した液を2−プロパノ−ルで2
5倍希釈して得た光触媒コ−ティング液Aを、上記洗浄
処理を施した窓ガラス表面にφ0.8mmのエアガンを
用いて105g/m2スプレ−コ−ティング法により塗
布後、20℃で20分乾燥させることにより、塗膜を硬
化させて、#19試料を得た。次に、#19試料につい
て水との接触角を調べた。その結果、水との接触角は0
゜まで超親水化された。Embodiment 16 FIG. Silicone facing north
After masking the area around the application surface of the window installed at the bottom of the runt to prevent the paint from scattering around, a cleaning agent containing an abrasive made of silicate minerals (TOTOKIKI, TOTO Powder) was wiped with a cloth impregnated with the powder) to remove colored stains and sealant stains. Next, after washing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, moisture adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, and 54.times.
8 parts by weight, 28 parts by weight of methanol and 7.2 parts of propanol
Parts by weight) and a photocatalyst coating liquid ST-K03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and propanol) Of a mixture consisting of 7.2 parts by weight of 2-propanol in 2-propanol.
The photocatalyst coating liquid A obtained by diluting 5-fold was applied to the surface of the window glass subjected to the above-mentioned washing treatment by a spray coating method of 105 g / m 2 using an air gun of φ0.8 mm. The coating was cured by drying for 20 minutes to obtain a # 19 sample. Next, the contact angle with water was examined for the # 19 sample. As a result, the contact angle with water is 0
It was superhydrophilized to ゜.
【0056】実施例17〜18;難溶性カルシウム塩に
起因する汚れが付着した鏡への適用 実施例17.難溶性カルシウム塩に起因する汚れが付着
して表面が白化した洗面鏡の塗布面周辺を、塗料の周辺
への飛散を防止するためにマスキングした後、塩酸水溶
液(pH2)を含浸させたウエスで、カルシウム塩付着
汚れを除去した。次いで、水道水で洗い流した後、水を
含浸させたウエスで窓を拭いて洗浄剤を除去し、さらに
ワイパ−及び乾いたウエスにて窓に付着する水分を除去
した。次いで、石原産業製光触媒コ−ティング液ST−
K01(酸化チタン粒子8重量部とエチルシリケ−ト2
重量部と硝酸水溶液54.8重量部とメタノ−ル28重
量部とプロパノ−ル7.2重量部からなる組成物)を2
−プロパノ−ルで25倍希釈して得た光触媒性コ−ティ
ング液を、上記洗浄処理を施した窓ガラス表面にφ0.
8mmのエアガンを用いて105g/m2スプレ−コ−
ティング法により塗布後、20℃で20分乾燥させるこ
とにより、塗膜を硬化させて、#20試料を得た。次
に、#20試料について水の濡れ性及び外観を調べた。
水との濡れ性は、鏡をハンドスプレーにて水を噴霧する
ことによって、水の濡れ性を測定した。その結果、噴霧
した水はウィンドウ上で水滴を形成すること無く、一様
な水膜を形成した。また、試料は透明であった。Examples 17 to 18; Application to mirrors with stains caused by poorly soluble calcium salts. After masking the area around the application surface of the wash mirror, which has a whitened surface due to adhesion of dirt caused by the hardly soluble calcium salt, to prevent scattering around the paint, use a cloth impregnated with an aqueous hydrochloric acid solution (pH 2). , And calcium salt adhered dirt was removed. Next, after washing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, moisture adhering to the window was removed with a wiper and a dry rag. Next, photocatalyst coating solution ST-
K01 (8 parts by weight of titanium oxide particles and ethyl silicate 2
2 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol)
-A photocatalytic coating solution obtained by diluting 25-fold with propanol was applied to the surface of a window glass having been subjected to the above-mentioned washing treatment to a diameter of 0.2 mm.
105 g / m 2 spray-coat using an 8 mm air gun
After coating by the coating method, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 20 sample. Next, the water wettability and appearance of the # 20 sample were examined.
The wettability with water was measured by spraying water with a hand spray on a mirror. As a result, the sprayed water formed a uniform water film without forming water droplets on the window. Also, the sample was transparent.
【0057】実施例18.難溶性カルシウム塩に起因す
る汚れが付着して表面が白化した洗面鏡の塗布面周辺
を、塗料の周辺への飛散を防止するためにマスキングし
た後、酸化セリウム研磨剤が添加されている洗浄剤を含
浸させたウエスで、カルシウム塩付着汚れを除去した。
次いで、水道水で洗い流した後、水を含浸させたウエス
で窓を拭いて洗浄剤を除去し、さらにワイパ−及び乾い
たウエスにて窓に付着する水分を除去した。次いで、石
原産業製光触媒コ−ティング液ST−K01(酸化チタ
ン粒子8重量部とエチルシリケ−ト2重量部と硝酸水溶
液54.8重量部とメタノ−ル28重量部とプロパノ−
ル7.2重量部からなる組成物)を2−プロパノ−ルで
25倍希釈して得た光触媒性コ−ティング液を、上記洗
浄処理を施した窓ガラス表面にφ0.8mmのエアガン
を用いて105g/m2スプレ−コ−ティング法により
塗布後、20℃で20分乾燥させることにより、塗膜を
硬化させて、#21試料を得た。次に、#21試料につ
いて水の濡れ性及び外観を調べた。水との濡れ性は、鏡
をハンドスプレーにて水を噴霧することによって、水の
濡れ性を測定した。その結果、噴霧した水はウィンドウ
上で水滴を形成すること無く、一様な水膜を形成した。
また、試料は透明であった。Embodiment 18 FIG. A cleaning agent containing a cerium oxide abrasive after masking the area around the application surface of the wash mirror, which has a whitened surface due to adhesion of dirt due to the hardly soluble calcium salt, to prevent scattering around the paint. The soil impregnated with calcium salt was removed with a waste impregnated with.
Next, after washing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, moisture adhering to the window was removed with a wiper and a dry rag. Then, a photocatalyst coating liquid ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of ethyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and propanol-
(A composition consisting of 7.2 parts by weight of toluene) was diluted 25-fold with 2-propanol, and the photocatalytic coating solution was applied to the surface of the window glass subjected to the above-mentioned washing treatment using an air gun of φ0.8 mm. After coating by a spray coating method of 105 g / m 2 , the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 21 sample. Next, the water wettability and appearance of the # 21 sample were examined. The wettability with water was measured by spraying water with a hand spray on a mirror. As a result, the sprayed water formed a uniform water film without forming water droplets on the window.
Also, the sample was transparent.
【0058】実施例19〜20;自動車窓ガラスへの適
用 実施例19.自動車リアウィンドウを、塗料の周辺への
飛散を防止するためにマスキングした後、酸化セリウム
研磨剤が添加されている洗浄剤を含浸させたウエスで拭
いて付着汚れを除去した。次いで、水を含浸させたウエ
スでウィンドウを拭いて洗浄剤を除去し、さらにワイパ
−及び乾いたウエスにてウィンドウに付着する水分を除
去した。次いで、石原産業製光触媒コ−ティング液ST
−K01(酸化チタン粒子8重量部とアルキルシリケ−
ト2重量部と硝酸水溶液54.8重量部とメタノ−ル2
8重量部とプロパノ−ル7.2重量部からなる組成物)
を1−プロパノ−ルで50倍希釈して得た光触媒コ−テ
ィング液を、上記洗浄処理を施したウィンドウ表面にφ
0.8mmのエアガンを用いて30g/m2スプレ−コ
−ティング法により塗布後、20℃で20分乾燥させる
ことにより、塗膜を硬化させて、#22試料を得た。次
に、#22試料について水の濡れ性及び外観を調べた。
水との濡れ性はウィンドウを、塗膜形成後、2日放置し
て太陽光に晒すことにより、紫外線が照射されるように
し、その後、ハンドスプレーにて水を噴霧することによ
って、水の濡れ性を測定した。その結果、噴霧した水は
ウィンドウ上で水滴を形成すること無く、一様な水膜を
形成した。また、試料は透明であった。Embodiments 19 to 20; Application to Automotive Window Glass Embodiment 19 After masking the rear window of the automobile to prevent the paint from scattering around, the adhered dirt was removed by wiping with a cloth impregnated with a detergent containing a cerium oxide abrasive. Next, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, water adhering to the window was removed with a wiper and a dry rag. Next, a photocatalyst coating solution ST manufactured by Ishihara Sangyo
-K01 (8 parts by weight of titanium oxide particles and alkyl silicate)
2 parts by weight, 54.8 parts by weight of an aqueous nitric acid solution and methanol 2
Composition comprising 8 parts by weight and 7.2 parts by weight of propanol)
Was diluted 50-fold with 1-propanol to give a photocatalyst coating solution on the surface of the window which had been subjected to the above-mentioned washing treatment.
After coating by a 30 g / m 2 spray coating method using an 0.8 mm air gun, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 22 sample. Next, the water wettability and appearance of the # 22 sample were examined.
The wettability with water is determined by exposing the window to ultraviolet light by leaving the window for two days after forming the coating film and exposing it to sunlight. The properties were measured. As a result, the sprayed water formed a uniform water film without forming water droplets on the window. Also, the sample was transparent.
【0059】実施例20.自動車リアウィンドウを、塗
料の周辺への飛散を防止するためにマスキングした後、
塩基性シリカゾル、モノエタノールアミン、ノニオン性
界面活性剤、グリコール系溶媒、エタノール、および水
からなる洗浄剤を含浸させたウエスでウィンドウを拭い
て付着汚れを除去した。次いで、石原産業製光触媒コ−
ティング液ST−K01(酸化チタン粒子8重量部とア
ルキルシリケ−ト2重量部と硝酸水溶液54.8重量部
とメタノ−ル28重量部とプロパノ−ル7.2重量部か
らなる組成物)を1−プロパノ−ル、レベリング剤から
なる混合溶媒(1−プロパノール90重量部、プロピレ
ングリコールエチルエーテル10重量部)で50倍希釈
して得た光触媒コ−ティング液を、上記洗浄処理を施し
たウィンドウ表面に、ポリプロピレン製不織布により塗
布後、20℃で20分乾燥させることにより、塗膜を硬
化させて、#23試料を得た。次に、#23試料につい
て水の濡れ性及び外観を調べた。水の濡れ性はウィンド
ウを、塗膜形成後、2日放置して太陽光に晒すことによ
り、紫外線が照射されるようにし、その後、ハンドスプ
レーにて水を噴霧することによって、水との濡れ性を測
定した。その結果、噴霧した水はウィンドウ上で水滴を
形成すること無く、一様な水膜を形成した。また、試料
は透明であった。Embodiment 20 FIG. After masking the rear window of the car to prevent paint from splashing around,
The window was wiped with a cloth impregnated with a cleaning agent composed of a basic silica sol, monoethanolamine, a nonionic surfactant, a glycol-based solvent, ethanol, and water to remove adhered dirt. Next, Ishihara Sangyo photocatalyst core
1 part of the liquid ST-K01 (composition comprising 8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol) -A window surface that has been subjected to the above-mentioned washing treatment with a photocatalyst coating liquid obtained by diluting 50-fold with a mixed solvent of propanol and a leveling agent (90 parts by weight of 1-propanol, 10 parts by weight of propylene glycol ethyl ether). After coating with a polypropylene nonwoven fabric, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 23 sample. Next, the water wettability and appearance of the # 23 sample were examined. The wettability of the water is measured by exposing the window to ultraviolet light by leaving the window for two days after forming the coating film and then exposing it to sunlight, and then spraying the water with a hand spray to wet the window. The properties were measured. As a result, the sprayed water formed a uniform water film without forming water droplets on the window. Also, the sample was transparent.
【0060】実施例21〜24;自動車ボディーへの適
用 実施例21.自動車のボンネットを、水を流しながら洗
車用スポンジで泥汚れを除去した後、ワックス塗布用ス
ポンジを用いて液体コンパウンド(武蔵ホルト製)でボ
ンネット表面を軽くこすった。コンパウンドが乾かない
うちにウェスで除去し、ボンネットを乾燥させた。次い
で、石原産業製光触媒コ−ティング液ST−K01(酸
化チタン粒子8重量部とアルキルシリケ−ト2重量部と
硝酸水溶液54.8重量部とメタノ−ル28重量部とプ
ロパノ−ル7.2重量部からなる組成物)を溶媒(2−
プロパノ−ル9重量部とジアセトンアルコール1重量部
との混合液)で100倍希釈して得た光触媒コ−ティン
グ液Bを、φ0.8mmのエアガンを用いて30g/m
2スプレ−コ−ティング法により塗布後、20℃で20
分乾燥させることにより、塗膜を硬化させて、#24試
料を得た。一方、比較のため、自動車のボンネットを、
水を流しながら洗車用スポンジで泥汚れを除去した後、
コンパウンド処理なしに、光触媒コ−ティング液Bを、
φ0.8mmのエアガンを用いて30g/m2スプレ−
コ−ティング法により塗布、20℃で20分乾燥させる
ことにより、塗膜を硬化させて、#25試料を得た。#
24、#25試料について塗布直後の外観を比較したと
ころ、#24試料は塗布前と同様であったのに対し、#
25試料は塗膜が白濁した。#24試料については、塗
膜形成後2日間太陽光に晒すことにより、紫外線が照射
されるようにした後、ハンドスプレーにて水を噴霧した
ところ、水滴が形成されず、水が一様に広がる様子が観
察された。Embodiments 21 to 24; Application to Automobile Body Embodiment 21 The bonnet of the automobile was cleaned with a car wash sponge while running water to remove mud and dirt, and the bonnet surface was lightly rubbed with a liquid compound (Musashi Holt) using a wax application sponge. Before the compound was dry, it was removed with a waste cloth and the bonnet was dried. Then, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) Parts) in a solvent (2-
A photocatalytic coating solution B obtained by diluting 100 times with a mixed solution of 9 parts by weight of propanol and 1 part by weight of diacetone alcohol) was obtained by using an air gun with a diameter of 0.8 mm to obtain 30 g / m 2.
2 After applying by spray coating method,
The coating film was hardened by minute drying to obtain # 24 sample. On the other hand, for comparison, the car hood
After removing dirt with a car wash sponge while running water,
Without compound treatment, the photocatalyst coating liquid B was
30 g / m 2 spray with air gun 0.8 mm in diameter -
The coating film was applied by a coating method and dried at 20 ° C. for 20 minutes to harden the coating film to obtain a # 25 sample. #
When the appearances of the 24 and # 25 samples were compared immediately after the application, the # 24 sample was the same as before the application, whereas the # 24 sample was the same as before the application.
In 25 samples, the coating film became cloudy. The # 24 sample was exposed to sunlight for 2 days after the coating film was formed, so that ultraviolet rays were irradiated. Then, water was sprayed using a hand spray. Spreading was observed.
【0061】実施例22.自動車のボンネットを、水を
流しながら洗車用スポンジで泥汚れを除去した後、ワッ
クス塗布用スポンジを用いて液体コンパウンド(武蔵ホ
ルト製)でボンネット表面を軽くこすった。コンパウン
ドが乾かないうちにウェスで除去し、ボンネットを乾燥
させた。次いで、コロイダルシリカゾル(日産化学製、
オルガノシリカゾル、IPA-ST)をイソプロパノールで希
釈し固形分濃度を0.3重量%とした液状体Cをスポン
ジ拭きにより塗布後、石原産業製光触媒コ−ティング液
ST−K01(酸化チタン粒子8重量部とアルキルシリ
ケ−ト2重量部と硝酸水溶液54.8重量部とメタノ−
ル28重量部とプロパノ−ル7.2重量部からなる組成
物)を溶媒(2−プロパノ−ル9重量部とジアセトンア
ルコール1重量部との混合液)で100倍希釈して得た
光触媒コ−ティング液Bを、φ0.8mmのエアガンを
用いて30g/m2スプレ−コ−ティング法により塗布
後、20℃で20分乾燥させることにより、塗膜を硬化
させて、#26試料を得た。一方、比較のため、自動車
のボンネットを、水を流しながら洗車用スポンジで泥汚
れを除去した後、コンパウンド処理なしに液状体Cをス
ポンジ拭きにより塗布し、光触媒コ−ティング液Bを、
φ0.8mmのエアガンを用いて30g/m2スプレ−
コ−ティング法により塗布、20℃で20分乾燥させる
ことにより、塗膜を硬化させて、#27試料を得た。#
26、#27試料について塗布直後の外観を比較したと
ころ、#26試料は塗布前と同様であったのに対し、#
27試料は塗膜が白濁した。#26試料については、塗
膜形成後3時間太陽光に晒すことにより、紫外線が照射
されるようにした後、ハンドスプレーにて水を噴霧した
ところ、水滴が形成されず、水が一様に広がる様子が観
察された。Embodiment 22 FIG. The bonnet of the automobile was cleaned with a car wash sponge while running water to remove mud and dirt, and the bonnet surface was lightly rubbed with a liquid compound (Musashi Holt) using a wax application sponge. Before the compound was dry, it was removed with a waste cloth and the bonnet was dried. Then, colloidal silica sol (Nissan Chemical,
After diluting organosilica sol, IPA-ST) with isopropanol and applying a liquid material C having a solid concentration of 0.3% by weight with a sponge wipe, the photocatalyst coating solution ST-K01 (titanium oxide particles 8% by weight) manufactured by Ishihara Sangyo Co., Ltd. Parts, 2 parts by weight of an alkyl silicate, 54.8 parts by weight of an aqueous nitric acid solution, and methanol
Photocatalyst obtained by diluting 100 parts of a solvent (composition comprising 9 parts by weight of 2-propanol and 1 part by weight of diacetone alcohol) with 28 parts by weight of toluene and 7.2 parts by weight of propanol. The coating liquid B was applied by a 30 g / m 2 spray coating method using an air gun having a diameter of 0.8 mm and then dried at 20 ° C. for 20 minutes to cure the coating film. Obtained. On the other hand, for comparison, after the bonnet of the automobile was washed with a car wash sponge while flowing water to remove mud and dirt, the liquid material C was applied by a sponge wipe without compound treatment, and the photocatalyst coating liquid B was applied.
30 g / m 2 spray with air gun 0.8 mm in diameter -
By coating by a coating method and drying at 20 ° C. for 20 minutes, the coating film was cured to obtain a # 27 sample. #
The appearance of the # 26 sample and the # 27 sample immediately after application were compared.
In 27 samples, the coating film became cloudy. For the # 26 sample, after being exposed to sunlight for 3 hours after the coating film was formed, ultraviolet rays were irradiated, and then water was sprayed with a hand spray. Spreading was observed.
【0062】実施例23.自動車のボンネットを、水を
かけて泥汚れを除去した後、無機微粒子研磨剤、アニオ
ン性界面活性剤が添加されている水系洗浄剤を、洗車用
スポンジを用いて軽くこするように洗浄した。水で充分
洗い流し、乾いたウェスで水分を拭き取った後、ボンネ
ットを乾燥させた。次いで、コロイダルシリカゾル(日
産化学製、オルガノシリカゾル、IPA-ST)をイソプロパ
ノールで希釈し固形分濃度を0.3重量%とした液状体
をスポンジ拭きにより塗布後、石原産業製光触媒コ−テ
ィング液ST−K01(酸化チタン粒子8重量部とアル
キルシリケ−ト2重量部と硝酸水溶液54.8重量部と
メタノ−ル28重量部とプロパノ−ル7.2重量部から
なる組成物)を溶媒(2−プロパノ−ル9重量部とジア
セトンアルコール1重量部との混合液)で100倍希釈
して得た光触媒コ−ティング液Bを、φ0.8mmのエ
アガンを用いて30g/m2スプレ−コ−ティング法に
より塗布後、20℃で20分乾燥させることにより、塗
膜を硬化させて、#28試料を得た。#28試料につい
ては、塗布直後の外観は塗布前と同様であった。また、
塗膜形成後3時間太陽光に晒すことにより、紫外線が照
射されるようにした後、ハンドスプレーにて水を噴霧し
たところ、水滴が形成されず、水が一様に広がる様子が
観察された。Embodiment 23 FIG. The hood of the automobile was washed with water to remove mud stains, and then washed with a water-based detergent to which an inorganic fine particle abrasive and an anionic surfactant had been added using a car wash sponge. After thoroughly washing with water and wiping off the moisture with a dry waste cloth, the bonnet was dried. Next, a colloidal silica sol (manufactured by Nissan Chemical Industries, organosilica sol, IPA-ST) was diluted with isopropanol to apply a liquid having a solid content of 0.3% by weight by a sponge wipe, and then coated with a photocatalyst coating solution ST manufactured by Ishihara Sangyo. -K01 (a composition comprising 8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of an aqueous nitric acid solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol) in a solvent (2- A photocatalyst coating solution B obtained by diluting 100 times with a mixed solution of 9 parts by weight of propanol and 1 part by weight of diacetone alcohol) was sprayed with a spray gun of 30 g / m 2 using an air gun of φ0.8 mm. After coating by the coating method, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain # 28 sample. For the # 28 sample, the appearance immediately after application was the same as before the application. Also,
After the coating film was formed, the film was exposed to sunlight for 3 hours to be irradiated with ultraviolet rays, and then water was sprayed with a hand spray. As a result, it was observed that water droplets were not formed and the water spread evenly. .
【0063】実施例24.自動車のボンネットを、水を
かけて泥汚れを除去した後、ノニオン系界面活性剤とア
ルカリ無機ビルダ−が添加されている水系洗浄剤(pH
11.9)を、洗車用スポンジを用いて軽くこするよう
に洗浄した。水で充分洗い流し、乾いたウェスで水分を
拭き取った後、ボンネットを乾燥させた。次いで、コロ
イダルシリカゾル(日産化学製、オルガノシリカゾル、
IPA-ST)をイソプロパノールで希釈し固形分濃度を0.
3重量%とした液状体をスポンジ拭きにより塗布後、石
原産業製光触媒コ−ティング液ST−K01(酸化チタ
ン粒子8重量部とアルキルシリケ−ト2重量部と硝酸水
溶液54.8重量部とメタノ−ル28重量部とプロパノ
−ル7.2重量部からなる組成物)を溶媒(2−プロパ
ノ−ル9重量部とジアセトンアルコール1重量部との混
合液)で100倍希釈して得た光触媒コ−ティング液B
を、φ0.8mmのエアガンを用いて30g/m2スプ
レ−コ−ティング法により塗布後、20℃で20分乾燥
させることにより、塗膜を硬化させて、#29試料を得
た。#29試料については、塗布直後の外観は塗布前と
同様であった。また、塗膜形成後3時間太陽光に晒すこ
とにより、紫外線が照射されるようにした後、ハンドス
プレーにて水を噴霧したところ、水滴が形成されず、水
が一様に広がる様子が観察された。Embodiment 24 FIG. Water is applied to the hood of the automobile to remove mud stains, and then an aqueous detergent (pH:
11.9) was washed by gently rubbing it with a car wash sponge. After thoroughly washing with water and wiping off the moisture with a dry waste cloth, the bonnet was dried. Next, colloidal silica sol (manufactured by Nissan Chemical Industries, organo silica sol,
(IPA-ST) is diluted with isopropanol to obtain a solid concentration of 0.
After applying a liquid material of 3% by weight with a sponge wipe, a photocatalyst coating solution ST-K01 manufactured by Ishihara Sangyo (8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of aqueous nitric acid solution, methanol Photocatalyst obtained by diluting 100 parts of a solvent (composition comprising 9 parts by weight of 2-propanol and 1 part by weight of diacetone alcohol) with 28 parts by weight of toluene and 7.2 parts by weight of propanol. Coating liquid B
Was applied by a 30 g / m 2 spray coating method using an air gun of φ0.8 mm, and then dried at 20 ° C. for 20 minutes to cure the coating film to obtain a # 29 sample. For the # 29 sample, the appearance immediately after application was the same as before the application. In addition, after the coating film was formed, it was exposed to sunlight for 3 hours so that ultraviolet rays were irradiated, and then water was sprayed with a hand spray. Was done.
【0064】実施例25〜26;シリコーンシーリング
材に起因する汚れが付着した窓ガラスへの適用 実施例25.北側に面したシリコ−ンシ−ラントの下部
に設置された窓の塗布面周辺を、塗料の周辺への飛散を
防止するためにマスキングした後、界面活性剤としてア
ルキルベンゼンスルホン酸ナトリウム及び脂肪酸アルカ
ノ−ルアミドが添加されている水系洗浄剤(pH9.
5)を含浸させたウエスで窓を拭いて有色付着汚れを除
去した。次いで、水道水で洗い流した後、水を含浸させ
たウエスで窓を拭いて洗浄剤を除去し、さらにワイパ−
及び乾いたウエスにて窓に付着する水分を除去した。そ
の後に、基材表面にプライマ−を塗布し、硬化させた。
次いで、石原産業製光触媒コ−ティング液STK01
(酸化チタン粒子8重量部とアルキルシリケ−ト2重量
部と硝酸水溶液54.8重量部とメタノ−ル28重量部
とプロパノ−ル7.2重量部からなる組成物)と石原産
業製光触媒コ−ティング液STK03(酸化チタン粒子
5重量部とアルキルシリケ−ト5重量部と硝酸水溶液5
4.8重量部とメタノ−ル28重量部とプロパノ−ル
7.2重量部からなる組成物)を1:1で混合した液を
2−プロパノ−ルで25倍希釈して得た光触媒コ−ティ
ング液Aを、上記洗浄処理を施した窓ガラス表面にφ
0.8mmのエアガンを用いて105g/m2スプレ−
コ−ティング法により塗布後、20℃で20分乾燥させ
ることにより、塗膜を硬化させて、#30試料を得た。
次に、#30試料について水との接触角を調べた。その
結果、水との接触角は0゜まで超親水化された。Examples 25 to 26: Application to window glass to which dirt caused by a silicone sealing material has adhered. After masking the area around the application surface of the window installed below the silicone sealant facing the north side to prevent the paint from scattering around the area, sodium alkylbenzenesulfonate and fatty acid alkanolamide are used as surfactants. Aqueous detergent (pH 9.
The window was wiped with a cloth impregnated with 5) to remove colored stains. Next, after rinsing with tap water, the window is wiped with a rag impregnated with water to remove the cleaning agent, and further wiped.
Then, water adhering to the window was removed with a dry waste cloth. Thereafter, a primer was applied to the surface of the base material and cured.
Next, a photocatalyst coating solution STK01 manufactured by Ishihara Sangyo Co., Ltd.
(A composition comprising 8 parts by weight of titanium oxide particles, 2 parts by weight of alkyl silicate, 54.8 parts by weight of nitric acid aqueous solution, 28 parts by weight of methanol and 7.2 parts by weight of propanol) and a photocatalyst core manufactured by Ishihara Sangyo Co., Ltd. Liquid STK03 (5 parts by weight of titanium oxide particles, 5 parts by weight of alkyl silicate and 5 parts of nitric acid aqueous solution)
A composition comprising 4.8 parts by weight, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) was mixed at a ratio of 1: 1 to obtain a photocatalyst core obtained by diluting 25-fold with 2-propanol. -Plating liquid A is applied to the surface of the window glass which has been subjected to the above-mentioned cleaning treatment by φ.
105 g / m 2 spray using a 0.8 mm air gun
After coating by a coating method, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 30 sample.
Next, the contact angle with water was examined for the # 30 sample. As a result, the contact angle with water was superhydrophilized to 0 °.
【0065】実施例26.北側に面したシリコ−ンシ−
ラントの下部に設置された窓の塗布面周辺を、塗料の周
辺への飛散を防止するためにマスキングした後、界面活
性剤としてアルキルベンゼンスルホン酸ナトリウム及び
脂肪酸アルカノ−ルアミドが添加されている水系洗浄剤
(pH9.5)を含浸させたウエスで窓を拭いて有色付
着汚れを除去した。次いで、水道水で洗い流した後、水
を含浸させたウエスで窓を拭いて洗浄剤を除去し、さら
にワイパ−及び乾いたウエスにて窓に付着する水分を除
去した。その後に、基材表面に500Wの水銀灯を照射
した。次いで、石原産業製光触媒コ−ティング液STK
01(酸化チタン粒子8重量部とアルキルシリケ−ト2
重量部と硝酸水溶液54.8重量部とメタノ−ル28重
量部とプロパノ−ル7.2重量部からなる組成物)と石
原産業製光触媒コ−ティング液STK03(酸化チタン
粒子5重量部とアルキルシリケ−ト5重量部と硝酸水溶
液54.8重量部とメタノ−ル28重量部とプロパノ−
ル7.2重量部からなる組成物)を1:1で混合した液
を2−プロパノ−ルで25倍希釈して得た光触媒コ−テ
ィング液Aを、上記洗浄処理を施した窓ガラス表面にφ
0.8mmのエアガンを用いて105g/m2スプレ−
コ−ティング法により塗布後、20℃で20分乾燥させ
ることにより、塗膜を硬化させて、#31試料を得た。
次に、#31試料について水との接触角を調べた。その
結果、水との接触角は0゜まで超親水化された。Embodiment 26 FIG. Silicone facing north
Aqueous detergent containing sodium alkylbenzenesulfonate and fatty acid alkanolamide as surfactants after masking the area around the application surface of the window installed at the bottom of the runt to prevent the paint from scattering around the area The window was wiped with a rag impregnated with (pH 9.5) to remove colored stains. Next, after washing with tap water, the window was wiped with a rag impregnated with water to remove the cleaning agent, and furthermore, moisture adhering to the window was removed with a wiper and a dry rag. Thereafter, the surface of the substrate was irradiated with a 500 W mercury lamp. Next, photocatalyst coating liquid STK manufactured by Ishihara Sangyo
01 (8 parts by weight of titanium oxide particles and alkyl silicate 2
Parts by weight, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol, and 7.2 parts by weight of propanol) and a photocatalyst coating liquid STK03 manufactured by Ishihara Sangyo (5 parts by weight of titanium oxide particles and alkyl silicate). -5 parts by weight, 54.8 parts by weight of a nitric acid aqueous solution, 28 parts by weight of methanol and propanol-
Of a photocatalyst coating solution A obtained by diluting a liquid obtained by mixing a 1: 1 mixture of the above-mentioned composition with 7.2 parts by weight with 2-propanol and subjecting the same to the above-mentioned cleaning treatment. To φ
105 g / m 2 spray using a 0.8 mm air gun
After coating by a coating method, the coating film was cured by drying at 20 ° C. for 20 minutes to obtain a # 31 sample.
Next, the contact angle with water was examined for the # 31 sample. As a result, the contact angle with water was superhydrophilized to 0 °.
【0066】[0066]
【発明の効果】本発明によれば、基材表面に付着してい
る汚れの影響でその上に形成される光触媒性親水性被膜
の表面の透明性、意匠性や親水性能が損なわれることが
生じなくなる。According to the present invention, the transparency, design and hydrophilicity of the surface of the photocatalytic hydrophilic film formed thereon may be impaired by the influence of dirt adhering to the substrate surface. No longer occurs.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI B32B 33/00 B32B 33/00 C09D 1/00 C09D 1/00 5/00 5/00 Z // B01J 35/02 B01J 35/02 J (72)発明者 山本 政宏 福岡県北九州市小倉北区中島2丁目1番1 号 東陶機器株式会社内──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification symbol FI B32B 33/00 B32B 33/00 C09D 1/00 C09D 1/00 5/00 5/00 Z 02 J (72) Inventor Masahiro Yamamoto 2-1-1 Nakajima, Kokurakita-ku, Kitakyushu-shi, Fukuoka
Claims (24)
光触媒性親水性コ−ティング液を塗布し、硬化せしめる
ことを特徴とする光触媒性親水性被膜の形成方法。After performing the step of cleaning the surface of the substrate,
A method for forming a photocatalytic hydrophilic coating, comprising applying a photocatalytic hydrophilic coating liquid and curing the coating.
群から選ばれる少なくとも1種を含有することを特徴と
する光触媒性親水性被膜形成用基材洗浄剤2. A substrate cleaning agent for forming a photocatalytic hydrophilic film, comprising at least one member selected from the group consisting of a surfactant, an abrasive, an acid, a base and a solvent.
とする光触媒性親水性被膜形成用基材洗浄剤3. A cleaning agent for forming a photocatalytic hydrophilic film, which comprises at least an abrasive.
塩基、溶剤の群から選ばれる少なくとも1種を含有する
ことを特徴とする光触媒性親水性被膜形成用基材洗浄剤4. At least an abrasive, a surfactant, an acid,
A base material detergent for forming a photocatalytic hydrophilic film, comprising at least one selected from the group consisting of a base and a solvent.
剤を必ず含むことを特徴とする請求項4に記載の光触媒
性親水性被膜形成用基材洗浄剤5. The cleaning agent for forming a photocatalytic hydrophilic film according to claim 4, wherein the surfactant always contains a nonionic surfactant.
であることを特徴とする請求項3に記載の光触媒性親水
性被膜形成用基材洗浄剤6. The cleaning agent for forming a photocatalytic hydrophilic film according to claim 3, wherein the abrasive has an average particle diameter of 10 μm or less.
基を含有することを特徴とする請求項2から6に記載の
光触媒性親水性被膜形成用基材洗浄剤7. The cleaning agent for forming a photocatalytic hydrophilic film according to claim 2, further comprising a base so as to have a pH of at least 10.
酸性フッ化カリウムから選ばれる少なくとも1種を含有
することを特徴とする請求項2から6に記載の光触媒性
親水性被膜形成用基材洗浄剤8. Hydrogen fluoride, ammonium acid fluoride,
The cleaning agent for forming a photocatalytic hydrophilic film according to any one of claims 2 to 6, further comprising at least one selected from potassium acid fluoride.
とする請求項1に記載の光触媒性親水性被膜の形成方法9. The method according to claim 1, wherein the substrate surface is a painted surface.
徴とする請求項2から7に記載の光触媒性親水性被膜形
成用基材洗浄剤10. The cleaning agent for forming a photocatalytic hydrophilic film according to claim 2, wherein the surface of the substrate is a painted surface.
を特徴とする請求項1に記載の光触媒性親水性被膜の形
成方法11. The method according to claim 1, wherein the surface of the substrate is a glass surface.
を特徴とする請求項2から8に記載の光触媒性親水性被
膜形成用基材洗浄剤12. The substrate cleaning agent for forming a photocatalytic hydrophilic film according to claim 2, wherein the substrate surface is a glass surface.
起因する汚れが付着した基材表面であることを特徴とす
る請求項2から8に記載の光触媒性親水性被膜形成用基
材洗浄剤13. The cleaning agent for forming a photocatalytic hydrophilic film according to claim 2, wherein the surface of the substrate is a surface of a substrate to which dirt caused by a sparingly soluble calcium salt is adhered.
起因する汚れが付着した基材表面であることを特徴とす
る請求項1に記載の光触媒性親水性被膜の形成方法14. The method for forming a photocatalytic hydrophilic film according to claim 1, wherein the surface of the substrate is a surface of a substrate to which dirt caused by a sparingly soluble calcium salt is adhered.
ガラス表面であることを特徴とする請求項2から8に記
載の光触媒性親水性被膜形成用基材洗浄剤15. The cleaning agent for forming a photocatalytic hydrophilic film according to claim 2, wherein the surface of the substrate is a surface of a window glass to which permanent dirt is adhered.
ガラス表面であることを特徴とする請求項1に記載の光
触媒性親水性被膜の形成方法16. The method for forming a photocatalytic hydrophilic film according to claim 1, wherein the surface of the substrate is a surface of a window glass to which permanent dirt is adhered.
材に起因する汚れが付着した基材表面であることを特徴
とする請求項2から8に記載の光触媒性親水性被膜形成
用基材洗浄剤17. The cleaning agent for forming a photocatalytic hydrophilic film according to claim 2, wherein the surface of the substrate is a surface of a substrate to which dirt caused by a silicone sealing material is adhered.
材に起因する汚れが付着した基材表面であることを特徴
とする請求項1に記載の光触媒性親水性被膜の形成方法18. The method according to claim 1, wherein the surface of the substrate is a surface of a substrate to which dirt caused by a silicone sealing material is adhered.
は、 (a)平均組成式 SiXqO(4-q)/2 (式中、Xはアルコキシ基、又は、ハロゲン原子であ
り、qは0<q<4を満足する数である)で表されるシ
リケ−トからなる塗膜形成要素であって、硬化させると
無定型シリカの被膜を形成するもの、(b)前記塗膜形
成要素中に分散され、光励起に応じて前記被膜の表面を
親水化するための光触媒性酸化物粒子、を含有すること
を特徴とする請求項1に記載の光触媒性親水性被膜の形
成方法。19. The photocatalytic hydrophilic coating liquid comprises: (a) an average composition formula SiX q O (4-q) / 2 (wherein X is an alkoxy group or a halogen atom, and q is (A number satisfying 0 <q <4), which forms a coating of amorphous silica when cured, and (b) the coating forming element The method for forming a photocatalytic hydrophilic film according to claim 1, further comprising photocatalytic oxide particles dispersed in the photocatalyst to hydrophilize the surface of the film in response to photoexcitation.
は、 (a)平均組成式 RpSiXqO(4-p-q)/2 (式中、Rは一価の有機基の1種若しくは2種以上から
なる官能基、又は、一価の有機基と水素基から選ばれた
2種以上からなる官能基であり、Xはアルコキシ基、又
は、ハロゲン原子であり、p及びqは0<p<2、0<
q<4を満足する数である)で表されるシロキサンから
なる塗膜形成要素であって、硬化させるとシリコ−ン樹
脂の被膜を形成するもの、(b)前記塗膜形成要素中に
分散され、光励起によって前記被膜の表面のシリコ−ン
分子中のケイ素原子に結合した有機基を光触媒作用によ
り少なくとも部分的に水酸基に置換させ、さらに光励起
に応じて被膜の表面を親水化するための光触媒性酸化物
粒子、を含有することを特徴とする請求項1に記載の光
触媒性親水性被膜の形成方法。20. The photocatalytic hydrophilic coating liquid comprises: (a) an average composition formula R p SiX q O (4-pq) / 2 (wherein R is one or two of a monovalent organic group) X is an alkoxy group or a halogen atom, and p and q are 0 <p. <2, 0 <
q <4), which forms a silicone resin film when cured, and (b) dispersed in the film forming element A photocatalyst for causing the organic group bonded to the silicon atom in the silicon molecule on the surface of the coating to be at least partially replaced with a hydroxyl group by photocatalysis by photoexcitation, and for hydrophilizing the surface of the coating in response to the photoexcitation. The method for forming a photocatalytic hydrophilic film according to claim 1, comprising a conductive oxide particle.
うち、少なくとも1種類と請求項19に記載のコーティ
ング液とからなる光触媒性親水性被膜形成材料21. A photocatalytic hydrophilic film-forming material comprising at least one of the cleaning agents according to claim 2 and the coating liquid according to claim 19.
うち、少なくとも1種類と請求項20に記載のコーティ
ング液とからなる光触媒性親水性被膜形成材料22. A photocatalytic hydrophilic film-forming material comprising at least one of the cleaning agents according to claim 2 and the coating liquid according to claim 20.
れが付着した基材表面に光触媒性親水性被膜の形成方法
する方法であって、その方法は基材表面を請求項2から
8に記載される洗浄剤のうち、少なくとも1種類からな
る洗浄液で洗浄して有色の汚れ成分を除去する工程、残
留シリコ−ン上をプライマ−により被覆する工程を行っ
た後に、請求項19または請求項20に記載の光触媒性
親水性コ−ティング液を塗布し硬化せしめることを特徴
とする光触媒性親水性被膜の形成方法。23. A method for forming a photocatalytic hydrophilic film on a surface of a substrate to which dirt caused by a silicone sealing material has adhered, wherein the method comprises applying the surface of the substrate to the surface of the substrate according to any one of claims 2 to 8. 21. The method according to claim 19, further comprising the step of removing colored stain components by washing with at least one kind of washing liquid among the washing agents to be performed, and the step of coating the remaining silicone with a primer. 5. A method for forming a photocatalytic hydrophilic coating, comprising applying and curing the photocatalytic hydrophilic coating liquid described in the above item 1.
れが付着した基材表面に光触媒性親水性被膜の形成方法
する方法であって、その方法は基材表面を請求項2から
8に記載される洗浄剤のうち、少なくとも1種類からな
る洗浄液で洗浄して有色の汚れ成分を除去する工程、残
留シリコ−ン表面に紫外線を照射する工程を行った後
に、請求項19または請求項20に記載の光触媒性親水
性コ−ティング液を塗布し硬化せしめることを特徴とす
る光触媒性親水性被膜の形成方法。24. A method for forming a photocatalytic hydrophilic film on a surface of a substrate to which dirt caused by a silicone sealing material has adhered. 21. The method according to claim 19, wherein after performing a step of removing colored contaminants by washing with at least one kind of washing liquid among the cleaning agents to be performed and a step of irradiating the surface of the residual silicone with ultraviolet rays, the method according to claim 19 or 20. A method for forming a photocatalytic hydrophilic coating, which comprises applying and curing the photocatalytic hydrophilic coating liquid as described above.
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11278798A JP3250607B2 (en) | 1997-04-08 | 1998-04-08 | Method for forming photocatalytic hydrophilic film, substrate cleaning agent for forming photocatalytic hydrophilic film, and photocatalytic hydrophilic film forming material |
CN98805787A CN1259162A (en) | 1997-06-04 | 1998-06-04 | Method for surface pretreatment before formation of photocatalytic hydrophilic film, and detergent and undercoat composition for use in the same |
PCT/JP1998/002487 WO1998055573A1 (en) | 1997-06-04 | 1998-06-04 | Method for surface pretreatment before formation of photocatalytic hydrophilic film, and detergent and undercoat composition for use in the same |
IL13294898A IL132948A0 (en) | 1997-06-04 | 1998-06-04 | Method for surface pretreatment before formation of photocatalytic hydrophilic film and detergent and undercoat composition for use in the same |
IDW991554A ID23407A (en) | 1997-06-04 | 1998-06-04 | INITIAL SURFACE TREATMENT METHODS BEFORE THE FORMATION OF THE PHOTOCATALISTING OF THE HYDROFIL AND CLEANING MATERIAL AND COMPOSITION OF THE LAYER LAYER FOR THE METHOD |
CA002290442A CA2290442A1 (en) | 1997-06-04 | 1998-06-04 | Method for surface pretreatment before formation of photocatalytic hydrophilic film, and detergent and undercoat composition for use in the same |
BR9810241-9A BR9810241A (en) | 1997-06-04 | 1998-06-04 | Cleaning agent to clean the surface of a substrate, composition of subcoat to form a subcoat on the surface of a substrate, process to form a photocatalytically hydrophilicable coating on the surface of a substrate, together, and, member |
AU75505/98A AU7550598A (en) | 1997-06-04 | 1998-06-04 | Method for surface pretreatment before formation of photocatalytic hydrophilic film, and detergent and undercoat composition for use in the same |
TW087108882A TW517082B (en) | 1997-06-04 | 1998-06-04 | A process for pre-treating the surface of a substrate before the formation of a photocatalytically hydrophilifiable coating, the cleaning agent used therein and the undercoating composition. |
EP98923133A EP0987317A1 (en) | 1997-06-04 | 1998-06-04 | Method for surface pretreatment before formation of photocatalytic hydrophilic film, and detergent and undercoat composition for use in the same |
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10512097 | 1997-04-08 | ||
JP10667897 | 1997-04-09 | ||
JP10667797 | 1997-04-09 | ||
JP9-106678 | 1997-04-09 | ||
JP9-106677 | 1997-04-09 | ||
JP9-105120 | 1997-04-09 | ||
JP11278798A JP3250607B2 (en) | 1997-04-08 | 1998-04-08 | Method for forming photocatalytic hydrophilic film, substrate cleaning agent for forming photocatalytic hydrophilic film, and photocatalytic hydrophilic film forming material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH10337526A true JPH10337526A (en) | 1998-12-22 |
JP3250607B2 JP3250607B2 (en) | 2002-01-28 |
Family
ID=27469289
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11278798A Expired - Lifetime JP3250607B2 (en) | 1997-04-08 | 1998-04-08 | Method for forming photocatalytic hydrophilic film, substrate cleaning agent for forming photocatalytic hydrophilic film, and photocatalytic hydrophilic film forming material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3250607B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010075762A (en) * | 2000-01-17 | 2001-08-11 | 김영웅 | the method coating titanium dioxide photo-catalyst on metal surface |
JP2006142206A (en) * | 2004-11-19 | 2006-06-08 | Murakami Corp | Photocatalyst-film carrying member |
WO2008056696A1 (en) * | 2006-11-08 | 2008-05-15 | Horiba, Ltd. | Washing storage solution for glass electrode and the like |
EP3150289A2 (en) | 2015-09-30 | 2017-04-05 | Toto Ltd. | Method for forming a coating film and a functional member comprising the coating film |
JP6389946B1 (en) * | 2017-11-02 | 2018-09-12 | アシストーン株式会社 | Stone painting method |
-
1998
- 1998-04-08 JP JP11278798A patent/JP3250607B2/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010075762A (en) * | 2000-01-17 | 2001-08-11 | 김영웅 | the method coating titanium dioxide photo-catalyst on metal surface |
JP2006142206A (en) * | 2004-11-19 | 2006-06-08 | Murakami Corp | Photocatalyst-film carrying member |
WO2008056696A1 (en) * | 2006-11-08 | 2008-05-15 | Horiba, Ltd. | Washing storage solution for glass electrode and the like |
JP4857288B2 (en) * | 2006-11-08 | 2012-01-18 | 株式会社堀場製作所 | Cleaning preservation solution for glass electrodes, etc. |
EP3150289A2 (en) | 2015-09-30 | 2017-04-05 | Toto Ltd. | Method for forming a coating film and a functional member comprising the coating film |
JP6389946B1 (en) * | 2017-11-02 | 2018-09-12 | アシストーン株式会社 | Stone painting method |
JP2019084477A (en) * | 2017-11-02 | 2019-06-06 | アシストーン株式会社 | Stone material coating method |
Also Published As
Publication number | Publication date |
---|---|
JP3250607B2 (en) | 2002-01-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TW517082B (en) | A process for pre-treating the surface of a substrate before the formation of a photocatalytically hydrophilifiable coating, the cleaning agent used therein and the undercoating composition. | |
JPH1150006A (en) | Pretreatment of surface forming photocalytic hydrophilic coating film and cleaning agent and unedrcoating composition used therefor | |
JPH11309379A (en) | Photocatalytic hydrophilic member and photocatalytic hydrophilic coating composition | |
JPH1191030A (en) | Hydrophilic member with photocatalystic property | |
JP3087682B2 (en) | Photocatalytic hydrophilic member | |
JP3264317B2 (en) | Photocatalytic hydrophilic member and method for producing the same | |
JP3250607B2 (en) | Method for forming photocatalytic hydrophilic film, substrate cleaning agent for forming photocatalytic hydrophilic film, and photocatalytic hydrophilic film forming material | |
JP3255346B2 (en) | Method for forming photocatalytic hydrophilic member, and photocatalytic hydrophilic member | |
JP3266535B2 (en) | Photocatalytic hydrophilic member, method for producing the same, and photocatalytic hydrophilic coating composition | |
JP3266526B2 (en) | Photocatalytic hydrophilic member and method for producing the same | |
JPH09227169A (en) | Transfer sheet, and transferring of photocatalytic and hydrophilic thin film | |
JP2001098187A (en) | Photocatalytic hydrophilic coating composition and method for preparing photocatalytic hydrophilic member | |
JP3303696B2 (en) | Photocatalytic hydrophilic coating composition | |
JP3298440B2 (en) | Photocatalytic hydrophilic coating liquid | |
JP2000086933A (en) | Photocatalytic hydrophilic material and photocatalytic hydrophilic coating composition | |
JP3173391B2 (en) | Hydrophilic film, and method for producing and using the same | |
JPH11100526A (en) | Photocatalytic hydrophilic member and photocatalytic hydrophilic coating composition | |
JPH09188850A (en) | Photocatalytic hydrophilic coating composition | |
JP3298439B2 (en) | Photocatalytic hydrophilic coating liquid | |
JPH10180948A (en) | Transfer sheet and method for transferring photocatalytic hydrophilic thin film | |
JP3348613B2 (en) | Photocatalytic hydrophilic coating composition | |
JP3109457B2 (en) | Photocatalytic hydrophilic member and photocatalytic hydrophilic coating composition | |
JP3844182B2 (en) | Hydrophilic film and method for producing and using the same | |
JPH1067543A (en) | Photocatalytic hydrophilic parts material | |
JP2000303055A (en) | Agent for restoring hydrophilicity of photocatalytic hydrophilic coating film |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
S201 | Request for registration of exclusive licence |
Free format text: JAPANESE INTERMEDIATE CODE: R314201 |
|
R360 | Written notification for declining of transfer of rights |
Free format text: JAPANESE INTERMEDIATE CODE: R360 |
|
R371 | Transfer withdrawn |
Free format text: JAPANESE INTERMEDIATE CODE: R371 |
|
S201 | Request for registration of exclusive licence |
Free format text: JAPANESE INTERMEDIATE CODE: R314201 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R314533 Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20071116 Year of fee payment: 6 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20071116 Year of fee payment: 6 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081116 Year of fee payment: 7 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081116 Year of fee payment: 7 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091116 Year of fee payment: 8 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091116 Year of fee payment: 8 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101116 Year of fee payment: 9 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101116 Year of fee payment: 9 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20111116 Year of fee payment: 10 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20111116 Year of fee payment: 10 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20111116 Year of fee payment: 10 |
|
S211 | Written request for registration of transfer of exclusive licence |
Free format text: JAPANESE INTERMEDIATE CODE: R314211 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20111116 Year of fee payment: 10 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20121116 Year of fee payment: 11 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20121116 Year of fee payment: 11 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20121116 Year of fee payment: 11 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20131116 Year of fee payment: 12 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20131116 Year of fee payment: 12 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20131116 Year of fee payment: 12 |
|
EXPY | Cancellation because of completion of term |