JPH09225263A - Air pollutant removing filter, air pollutant removing fan and ventilator using the fan - Google Patents
Air pollutant removing filter, air pollutant removing fan and ventilator using the fanInfo
- Publication number
- JPH09225263A JPH09225263A JP8150410A JP15041096A JPH09225263A JP H09225263 A JPH09225263 A JP H09225263A JP 8150410 A JP8150410 A JP 8150410A JP 15041096 A JP15041096 A JP 15041096A JP H09225263 A JPH09225263 A JP H09225263A
- Authority
- JP
- Japan
- Prior art keywords
- filter
- fan
- air pollutants
- air pollutant
- removing air
- 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.)
- Pending
Links
- 239000000809 air pollutant Substances 0.000 title claims abstract description 55
- 231100001243 air pollutant Toxicity 0.000 title claims abstract description 55
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 44
- 239000000463 material Substances 0.000 claims abstract description 25
- 239000000126 substance Substances 0.000 claims abstract description 23
- 238000009423 ventilation Methods 0.000 claims description 34
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 24
- 239000010410 layer Substances 0.000 claims description 21
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 20
- 239000011941 photocatalyst Substances 0.000 claims description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 8
- 229920002050 silicone resin Polymers 0.000 claims description 5
- 230000001678 irradiating effect Effects 0.000 claims description 4
- 229910052763 palladium Inorganic materials 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- -1 polyhydroxysiloxane Polymers 0.000 claims description 4
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 4
- 229910001887 tin oxide Inorganic materials 0.000 claims description 4
- 239000002344 surface layer Substances 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052737 gold Inorganic materials 0.000 claims description 2
- 239000010931 gold Substances 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims 1
- 230000001699 photocatalysis Effects 0.000 abstract description 14
- 238000005406 washing Methods 0.000 abstract description 12
- 230000008859 change Effects 0.000 abstract description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 11
- 239000007789 gas Substances 0.000 description 9
- 230000002209 hydrophobic effect Effects 0.000 description 8
- 238000000354 decomposition reaction Methods 0.000 description 6
- 239000000123 paper Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 230000005284 excitation Effects 0.000 description 3
- 150000004687 hexahydrates Chemical class 0.000 description 3
- 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 3
- 239000000843 powder Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000013076 target substance Substances 0.000 description 3
- 239000012780 transparent material Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- NWFNSTOSIVLCJA-UHFFFAOYSA-L copper;diacetate;hydrate Chemical compound O.[Cu+2].CC([O-])=O.CC([O-])=O NWFNSTOSIVLCJA-UHFFFAOYSA-L 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 2
- 238000007539 photo-oxidation reaction Methods 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 229910000077 silane 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
- 239000010802 sludge Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- HXLAEGYMDGUSBD-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propan-1-amine Chemical compound CCO[Si](C)(OCC)CCCN HXLAEGYMDGUSBD-UHFFFAOYSA-N 0.000 description 1
- UDWIZRDPCQAYRF-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propyl prop-2-enoate Chemical compound CCO[Si](C)(OCC)CCCOC(=O)C=C UDWIZRDPCQAYRF-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
- XDQWJFXZTAWJST-UHFFFAOYSA-N 3-triethoxysilylpropyl prop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C=C XDQWJFXZTAWJST-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- GLDPGGLLQUPPPH-UHFFFAOYSA-N C(C)O[Si](OCC)(OCC)OCC.CO[Si](OC)(OC)OC.Br[Si](Br)(Br)Br.Cl[Si](Cl)(Cl)Cl.C1(=CC=CC=C1)[Si](OCC)(OCC)OCC.C1(=CC=CC=C1)[Si](OC)(OC)OC.C1(=CC=CC=C1)[Si](Br)(Br)Br.C1(=CC=CC=C1)[Si](Cl)(Cl)Cl.C(CCCCCCCCCCCCCCCCC)[Si](OCC)(OCC)OCC Chemical compound C(C)O[Si](OCC)(OCC)OCC.CO[Si](OC)(OC)OC.Br[Si](Br)(Br)Br.Cl[Si](Cl)(Cl)Cl.C1(=CC=CC=C1)[Si](OCC)(OCC)OCC.C1(=CC=CC=C1)[Si](OC)(OC)OC.C1(=CC=CC=C1)[Si](Br)(Br)Br.C1(=CC=CC=C1)[Si](Cl)(Cl)Cl.C(CCCCCCCCCCCCCCCCC)[Si](OCC)(OCC)OCC GLDPGGLLQUPPPH-UHFFFAOYSA-N 0.000 description 1
- JSJVPYUECUEVET-UHFFFAOYSA-N C(CCCCC)[Si](Cl)(Cl)Cl.C(CC)[Si](OC(C)C)(OC(C)C)OC(C)C.C(CC)[Si](OCC)(OCC)OCC.C(CC)[Si](OC)(OC)OC.C(CC)[Si](Br)(Br)Br.C(CC)[Si](Cl)(Cl)Cl.C(C)[Si](OC(C)C)(OC(C)C)OC(C)C.C(C)O[SiH](OCC)OCC Chemical compound C(CCCCC)[Si](Cl)(Cl)Cl.C(CC)[Si](OC(C)C)(OC(C)C)OC(C)C.C(CC)[Si](OCC)(OCC)OCC.C(CC)[Si](OC)(OC)OC.C(CC)[Si](Br)(Br)Br.C(CC)[Si](Cl)(Cl)Cl.C(C)[Si](OC(C)C)(OC(C)C)OC(C)C.C(C)O[SiH](OCC)OCC JSJVPYUECUEVET-UHFFFAOYSA-N 0.000 description 1
- WIJQGKRFCKTZMC-UHFFFAOYSA-N C(CCCCCCCCC)[Si](OCC)(OCC)OCC.C(CCCCCCCCC)[Si](OC)(OC)OC.C(CCCCC)[Si](OCC)(OCC)OCC.C(CCCCC)[Si](OC)(OC)OC.C(CCCCC)[Si](Br)(Br)Br Chemical compound C(CCCCCCCCC)[Si](OCC)(OCC)OCC.C(CCCCCCCCC)[Si](OC)(OC)OC.C(CCCCC)[Si](OCC)(OCC)OCC.C(CCCCC)[Si](OC)(OC)OC.C(CCCCC)[Si](Br)(Br)Br WIJQGKRFCKTZMC-UHFFFAOYSA-N 0.000 description 1
- KVRZJLOGPINXKQ-UHFFFAOYSA-N C1(=CC=CC=C1)C[SiH](OCC)OCC.C1(=CC=CC=C1)C[SiH](OC)OC.C1(=CC=CC=C1)C[SiH](Br)Br.C1(=CC=CC=C1)C[SiH](Cl)Cl.C1(=CC=CC=C1)[Si](OCC)(OCC)C1=CC=CC=C1.C1(=CC=CC=C1)[Si](OC)(OC)C1=CC=CC=C1 Chemical compound C1(=CC=CC=C1)C[SiH](OCC)OCC.C1(=CC=CC=C1)C[SiH](OC)OC.C1(=CC=CC=C1)C[SiH](Br)Br.C1(=CC=CC=C1)C[SiH](Cl)Cl.C1(=CC=CC=C1)[Si](OCC)(OCC)C1=CC=CC=C1.C1(=CC=CC=C1)[Si](OC)(OC)C1=CC=CC=C1 KVRZJLOGPINXKQ-UHFFFAOYSA-N 0.000 description 1
- VYOQTQNGUXNZLD-UHFFFAOYSA-N C1(=CC=CC=C1)[Si](Br)(Br)C1=CC=CC=C1.C1(=CC=CC=C1)[Si](Cl)(Cl)C1=CC=CC=C1.C[Si](OCC)(OCC)C.C[Si](OC)(OC)C.C[Si](Br)(Br)C.C[Si](Cl)(Cl)C.CO[Si](OCC)(OCC)OC.CO[Si](OCC)(OCC)OC Chemical compound C1(=CC=CC=C1)[Si](Br)(Br)C1=CC=CC=C1.C1(=CC=CC=C1)[Si](Cl)(Cl)C1=CC=CC=C1.C[Si](OCC)(OCC)C.C[Si](OC)(OC)C.C[Si](Br)(Br)C.C[Si](Cl)(Cl)C.CO[Si](OCC)(OCC)OC.CO[Si](OCC)(OCC)OC VYOQTQNGUXNZLD-UHFFFAOYSA-N 0.000 description 1
- RXFVSVHLVGNIRI-UHFFFAOYSA-N FC(CC[Si](Br)(Br)Br)(F)F.FC(CC[Si](Cl)(Cl)Cl)(F)F.C(=C)[Si](OCC)(OCC)OCC.C(=C)[Si](OC)(OC)OC.C(=C)[Si](Br)(Br)Br.[SiH4].C(=C)[Si](Cl)(Cl)Cl.SCCC[Si](OCC)(OCC)OCC Chemical compound FC(CC[Si](Br)(Br)Br)(F)F.FC(CC[Si](Cl)(Cl)Cl)(F)F.C(=C)[Si](OCC)(OCC)OCC.C(=C)[Si](OC)(OC)OC.C(=C)[Si](Br)(Br)Br.[SiH4].C(=C)[Si](Cl)(Cl)Cl.SCCC[Si](OCC)(OCC)OCC RXFVSVHLVGNIRI-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- PTHGSOGQNNUSME-UHFFFAOYSA-N [H+].[SiH4].[Br-].Br.Br Chemical compound [H+].[SiH4].[Br-].Br.Br PTHGSOGQNNUSME-UHFFFAOYSA-N 0.000 description 1
- RMKZLFMHXZAGTM-UHFFFAOYSA-N [dimethoxy(propyl)silyl]oxymethyl prop-2-enoate Chemical compound CCC[Si](OC)(OC)OCOC(=O)C=C RMKZLFMHXZAGTM-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000000274 adsorptive effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 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
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002772 conduction electron Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- OTARVPUIYXHRRB-UHFFFAOYSA-N diethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](C)(OCC)CCCOCC1CO1 OTARVPUIYXHRRB-UHFFFAOYSA-N 0.000 description 1
- WHGNXNCOTZPEEK-UHFFFAOYSA-N dimethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](C)(OC)CCCOCC1CO1 WHGNXNCOTZPEEK-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 239000005055 methyl trichlorosilane Substances 0.000 description 1
- HLXDKGBELJJMHR-UHFFFAOYSA-N methyl-tri(propan-2-yloxy)silane Chemical compound CC(C)O[Si](C)(OC(C)C)OC(C)C HLXDKGBELJJMHR-UHFFFAOYSA-N 0.000 description 1
- AHQDZKRRVNGIQL-UHFFFAOYSA-N methyl-tris[(2-methylpropan-2-yl)oxy]silane Chemical compound CC(C)(C)O[Si](C)(OC(C)(C)C)OC(C)(C)C AHQDZKRRVNGIQL-UHFFFAOYSA-N 0.000 description 1
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000013032 photocatalytic reaction Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000003075 superhydrophobic effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- UQMOLLPKNHFRAC-UHFFFAOYSA-N tetrabutyl silicate Chemical compound CCCCO[Si](OCCCC)(OCCCC)OCCCC UQMOLLPKNHFRAC-UHFFFAOYSA-N 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- KVENDAGPVNAYLY-UHFFFAOYSA-N tribromo(ethyl)silane Chemical compound CC[Si](Br)(Br)Br KVENDAGPVNAYLY-UHFFFAOYSA-N 0.000 description 1
- KBSUPJLTDMARAI-UHFFFAOYSA-N tribromo(methyl)silane Chemical compound C[Si](Br)(Br)Br KBSUPJLTDMARAI-UHFFFAOYSA-N 0.000 description 1
- ZOYFEXPFPVDYIS-UHFFFAOYSA-N trichloro(ethyl)silane Chemical compound CC[Si](Cl)(Cl)Cl ZOYFEXPFPVDYIS-UHFFFAOYSA-N 0.000 description 1
- ZLGWXNBXAXOQBG-UHFFFAOYSA-N triethoxy(3,3,3-trifluoropropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCC(F)(F)F ZLGWXNBXAXOQBG-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
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- JLGNHOJUQFHYEZ-UHFFFAOYSA-N trimethoxy(3,3,3-trifluoropropyl)silane Chemical compound CO[Si](OC)(OC)CCC(F)(F)F JLGNHOJUQFHYEZ-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F28—HEAT EXCHANGE IN GENERAL
- F28F—DETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
- F28F13/00—Arrangements for modifying heat-transfer, e.g. increasing, decreasing
- F28F13/18—Arrangements for modifying heat-transfer, e.g. increasing, decreasing by applying coatings, e.g. radiation-absorbing, radiation-reflecting; by surface treatment, e.g. polishing
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F8/00—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying
- F24F8/20—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying by sterilisation
- F24F8/22—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying by sterilisation using UV light
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F28—HEAT EXCHANGE IN GENERAL
- F28F—DETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
- F28F2245/00—Coatings; Surface treatments
- F28F2245/02—Coatings; Surface treatments hydrophilic
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Catalysts (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、空気中の汚染物質
を光触媒作用により化学変化させて捕捉・除去する機能
を有する大気汚染物質除去用フィルター、大気汚染物質
除去用ファン又は換気装置に関する。特には、化学変化
生成物の水洗による除去性に優れ、被対象物質を長期に
わたって有効に除去しうる大気汚染物質除去用フィルタ
ー、大気汚染物質除去用ファン又は換気装置に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an air pollutant removal filter, a fan for removing air pollutants, or a ventilation device having a function of chemically changing and capturing and removing pollutants in the air by photocatalytic action. In particular, the present invention relates to an air pollutant removal filter, an air pollutant removal fan, or a ventilation device that has excellent removability of a chemical change product by washing with water and can effectively remove a target substance for a long period of time.
【0002】[0002]
【従来の技術】都市部の外気取入れ用換気扇は、有害な
大気汚染物質であるNOx やSOx 、悪臭物質を除去し
た上で外気を取入れることが、居住者の健康上あるいは
生活環境上好ましい。そのような大気汚染物質除去機能
を有する従来の換気扇フィルターの最もポピュラーなも
のは、活性炭により上記大気汚染物質を吸着除去する方
式を採用している。したがって、使用している活性炭の
吸着量が飽和すると、大気汚染物質除去機能を発揮しな
くなり、活性炭あるいはフィルター全体を交換する必要
があった。2. Description of the Related Art In a ventilation fan for taking in outside air in urban areas, it is necessary to remove harmful air pollutants such as NO x and SO x and odorous substances before taking in outside air for the health of residents and the living environment. preferable. The most popular conventional ventilation fan filter having such an air pollutant removal function employs a method of adsorbing and removing the above air pollutants by activated carbon. Therefore, when the adsorbed amount of the activated carbon used is saturated, the function of removing air pollutants is not exerted, and it is necessary to replace the activated carbon or the entire filter.
【0003】一方、大気汚染物質を光触媒により分解除
去する方法は、従来より知られている(特開平6−31
5614)。また、光触媒、あるいは光触媒と活性炭に
より室内空気を浄化する空気清浄機(特開平3−607
20)や換気装置(特開平7−280314)も提案さ
れている。On the other hand, a method of decomposing and removing air pollutants by a photocatalyst is conventionally known (Japanese Patent Laid-Open No. 6-31).
5614). Further, an air purifier that purifies indoor air with a photocatalyst or a photocatalyst and activated carbon (Japanese Patent Laid-Open No. 3-607).
20) and a ventilation device (JP-A-7-280314).
【0004】[0004]
【発明が解決しようとする課題】しかしながら、特開平
6−315614の方法を、換気装置のような室内装置
に適用しようとすると、NOx の分解で生成する硝酸
や、SOx の分解で生成する硫酸を、光触媒表面から除
去する有効な手段を有しないため、ある期間使用すると
光触媒活性の低下を招く。その他、油煙等の未分解物も
吸着するであろうから、光触媒活性の低下はより進行
し、かつ上記付着物による遮光効果も加わるため、機能
低下は加速的に進行すると考えられる。このような問題
点は、特開平3−60720の空気清浄機や、特開平7
−280314の換気装置にも共通する。However, when the method of Japanese Patent Laid-Open No. 6-315614 is applied to an indoor unit such as a ventilator, nitric acid produced by decomposition of NO x or SO x is produced. Since it does not have an effective means of removing sulfuric acid from the photocatalyst surface, it leads to a decrease in photocatalytic activity when used for a certain period of time. In addition, since undegraded substances such as oil smoke will also be adsorbed, the photocatalytic activity is further reduced, and the light-shielding effect by the attached substances is also added, so that it is considered that the functional degradation is accelerated. Such a problem is caused by the air cleaner disclosed in JP-A-3-60720 and the JP-A-7-60720.
It is also common to the -280314 ventilation system.
【0005】光触媒作用に基づく大気汚染物質除去機能
を有するフィルター等が汚れた場合、フィルター等を洗
浄することで該機能を回復できる。しかし、活性の高い
光触媒は比較的低温で基材に固定化されているもので、
通常多孔質体であり、基材に強固に固定することは困難
であるため、光触媒物質を付着したフィルターの表面を
ブラシ等を用いて洗浄すると、ブラッシング力によって
容易に光触媒物質層が脱落し、機能低下を生じるという
問題があった。When a filter or the like having an air pollutant removing function based on a photocatalytic action becomes dirty, the function can be restored by washing the filter and the like. However, a highly active photocatalyst is immobilized on a substrate at a relatively low temperature,
Since it is usually a porous body and it is difficult to firmly fix it to the substrate, if the surface of the filter to which the photocatalyst substance is attached is washed using a brush or the like, the photocatalyst substance layer easily falls off due to the brushing force, There was a problem that the function deteriorated.
【0006】本発明は、化学変化生成物の水洗による除
去性に優れ、被対象物質を長期にわたって有効に除去し
うる大気汚染物質除去用フィルター、大気汚染物質除去
用ファン又は換気装置を提供することを目的とする。The present invention provides an air pollutant removal filter, an air pollutant removal fan, or a ventilation device which has excellent removability of a chemical change product by washing with water and can effectively remove a target substance for a long period of time. With the goal.
【0007】[0007]
【課題を解決するための手段】第一に、本発明者は、部
材表面に付着する物質の性質と、該部材表面の水との接
触角との間に図7に示す関係があることを見出した。図
7の横軸は、部材表面と水との接触角を示し、縦軸は、
水洗→乾燥の繰り返し後における部材表面の付着汚れの
程度を示す。親水性の汚れについては、接触角が0°近
辺と80°以上が汚れが少ない。両性物質汚れについて
は、接触角20°以下と140°以上が汚れが少ない。
疎水性の汚れについては、接触角60°以下と180°
近辺が汚れが少ない。図7より、結局全ての性質の付着
物をきれいに水洗しうる表面を得るには、水との接触角
が5°未満(後述実施例5参照)の超親水性表面にする
か、同角が180°に近い超撥水性表面にする必要があ
ることが分る。すなわち、水との接触角を5°未満の超
親水性表面にすれば、付着物の性質に依らず、付着した
分解生成物を効果的に除去しうる。この方法によれば、
対象物が緻密体である場合のみでなく、通気性のフィル
ターのような多孔質のものの場合でも、フィルター材質
が疎水性であると水洗しても材料が水を弾き、細孔中に
水が入っていかないため細孔中に詰まった汚染物質が除
去できないのに対して、超親水化したものでは細孔中の
汚染物質が水洗で容易に除去できる効果を発揮する。First, the present inventor has found that there is a relationship shown in FIG. 7 between the property of a substance adhering to the surface of a member and the contact angle of the surface of the member with water. I found it. The horizontal axis in FIG. 7 represents the contact angle between the surface of the member and water, and the vertical axis represents
Indicates the degree of stains on the surface of the member after repeated washing and drying. With respect to hydrophilic stains, there is little stain when the contact angle is around 0 ° and 80 ° or more. Regarding amphoteric substance stains, there is little stain at contact angles of 20 ° or less and 140 ° or more.
Contact angle 60 ° or less and 180 ° for hydrophobic stains
There is little dirt in the vicinity. From FIG. 7, after all, in order to obtain a surface on which deposits of all properties can be washed cleanly with water, a superhydrophilic surface having a contact angle with water of less than 5 ° (see Example 5 described later) is used, or the same angle is used. It turns out that it is necessary to have a superhydrophobic surface close to 180 °. That is, when the superhydrophilic surface has a contact angle with water of less than 5 °, the attached decomposition products can be effectively removed regardless of the nature of the attached material. According to this method
Not only when the object is a dense body but also when it is a porous material such as a breathable filter, if the filter material is hydrophobic, the material repels water even if it is washed with water, and the water is left in the pores. The contaminants clogged in the pores cannot be removed because they do not enter, whereas the superhydrophilized one exhibits the effect that the contaminants in the pores can be easily removed by washing with water.
【0008】第二に本発明者は、部材の表面に酸化チタ
ン等の光半導体が存在すると、該表面に励起波長以下の
フォトンが照射されることにより、伝導電子と正孔が生
成し、それによりおそらく表面の極性が生じることによ
り、表面の親水性が維持・回復されることを見出した。
したがって、酸化チタン等の光半導体が存在し、かつ発
明の実施の形態において例示するようなある条件を満足
する場合には、部材表面に上記光を照射すれば、表面を
水との接触角が5°未満の超親水性状態に維持・回復し
うる。Secondly, the present inventor has found that when an optical semiconductor such as titanium oxide is present on the surface of a member, the surface is irradiated with photons having an excitation wavelength or less to generate conduction electrons and holes. It was found that the surface hydrophilicity is maintained / restored, probably due to the surface polarity.
Therefore, when an optical semiconductor such as titanium oxide is present and a certain condition as exemplified in the embodiment of the invention is satisfied, when the surface of the member is irradiated with the above light, the contact angle with water on the surface becomes It is possible to maintain and recover the superhydrophilic state of less than 5 °.
【0009】すなわち、本発明の大気汚染物質除去用フ
ィルターは、表面に光触媒含有層が形成された通気性の
基材からなり、 該表面は、水との接触角が5°未満の
親水性であることを特徴とする。That is, the filter for removing air pollutants of the present invention comprises an air-permeable base material having a photocatalyst-containing layer formed on the surface thereof, and the surface is hydrophilic and has a contact angle with water of less than 5 °. It is characterized by being.
【0010】また、本発明の大気汚染物質除去用ファン
は、表面に光触媒含有層が形成された基材からなる羽根
を有し、 該表面の水との接触角が5°未満の親水性で
あることを特徴とする。Further, the fan for removing air pollutants of the present invention has blades made of a base material having a photocatalyst-containing layer formed on the surface thereof, and has a hydrophilic surface having a contact angle with water of less than 5 °. It is characterized by being.
【0011】さらに、本発明の換気装置は、上記の大気
汚染物質除去用フィルター及び/又は大気汚染物質除去
用ファンを有し、 該フィルター及び/又はファンが屋
外光の照射を受けうる状態に配置されているか、該フィ
ルター及び/又はファンに紫外線を照射する手段が設け
られていることを特徴とする。Further, the ventilation device of the present invention has the above-mentioned filter for removing air pollutants and / or a fan for removing air pollutants, and the filter and / or fan is arranged in a state in which it can be irradiated with outdoor light. Or a means for irradiating the filter and / or the fan with ultraviolet rays is provided.
【0012】[0012]
(1)部材表面と水との接触角が5°未満の超親水性表
面にする方法としては以下を挙げることができる。 部材表面に、酸化チタンと酸化スズからなる層を形
成する方法である。このような層の形成方法としては、
例えば、酸化チタンゾルと酸化スズゾルを混合し、基材
に塗布し、焼成する。 部材表面に、酸化チタンと酸化ケイ素からなる層を
形成する方法である。このような層の形成方法として
は、例えば、酸化チタンゾルとコロイダルシリカを混合
し、基材に塗布し、焼成する。(1) The following may be mentioned as a method of forming a superhydrophilic surface in which the contact angle between the member surface and water is less than 5 °. This is a method of forming a layer composed of titanium oxide and tin oxide on the surface of a member. As a method of forming such a layer,
For example, titanium oxide sol and tin oxide sol are mixed, applied to a base material, and baked. This is a method of forming a layer composed of titanium oxide and silicon oxide on the surface of a member. As a method of forming such a layer, for example, titanium oxide sol and colloidal silica are mixed, coated on a base material, and baked.
【0013】 部材表面に、酸化チタンとシリコーン
樹脂からなる混合層を形成後、励起波長以下のフォトン
を照射して混合層の少なくとも最表面に存するシリコー
ン樹脂を、ヒドロキシシロキサンに変化させる方法であ
る。このような層の形成方法としては、例えば、まず、
オルガノアルコキシシランと酸化チタンを混合し、基材
に塗布し、オルガノアルコキシシランを加水分解、脱水
縮重合させて、ポリオルガノシロキサンと酸化チタンか
らなる混合層を形成する。その後、励起波長以下のフォ
トンを照射して混合層の少なくとも最表面に存するオル
ガノ基を水酸基に置換させる。This is a method of forming a mixed layer composed of titanium oxide and a silicone resin on the surface of a member, and then irradiating a photon having an excitation wavelength or less to change the silicone resin present on at least the outermost surface of the mixed layer to hydroxysiloxane. As a method for forming such a layer, for example, first,
Organoalkoxysilane and titanium oxide are mixed and coated on a substrate, and the organoalkoxysilane is hydrolyzed and dehydrated and polycondensed to form a mixed layer of polyorganosiloxane and titanium oxide. Then, photons having an excitation wavelength or less are irradiated to replace at least the outermost organo group of the mixed layer with a hydroxyl group.
【0014】ここで、シリコーン樹脂は、加水分解性基
を2〜4個有するシランの加水分解縮合物を含むもので
ある。その原料となる加水分解性シランの例としては、 メチルトリクロルシラン メチルトリブロムシラン メチルトリメトキシシラン メチルトリエトキシシラン メチルトリイソプロポキシシラン メチルトリt−ブトキシシラン エチルトリクロルシラン エチルトリブロムシラン エチルトリメトキシシラン エチルトリエトキシシラン エチルトリイソプロポキシシラン n−プロピルトリクロルシラン n−プロピルトリブロムシラン 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−プロピルトリイソプロポキシシラン n−ヘキシルトリクロルシラン n−ヘキシルトリブロムシラン n−ヘキシルトリメトキシシラン n−ヘキシルトリエトキシシラン n−デシルトリメトキシシラン n−デシルトリエトキシシラン n−オクタデシルトリメトキシシラン n−オクタデシルトリエトキシシラン フェニルトリクロルシラン フェニルトリブロムシラン 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 テトラクロルシラン テトラブロムシラン テトラメトキシシラン テトラエトキシシラン テトラブトキシシラン ジメトキシジエトキシシラン ジメトキシジエトキシシラン ジメチルジクロルシラン ジメチルジブロムシラン ジメチルジメトキシシラン ジメチルジエトキシシラン ジフェニルジクロルシラン ジフェニルジブロムシラン ジフェニルジメトキシシラン ジフェニルジエトキシシラン フェニルメチルジクロルシラン フェニルメチルジブロムシラン 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 トリクロルヒドロシラン トリブロムヒドロシラン トリメトキシヒドロシラン トリエトキシヒドロシラン γ−グリシドキシプロピルトリメトキシシラン γ−グリシドキシプロピルトリエトキシシラン γ−グリシドキシプロピルメチルジメトキシシラン γ−グリシドキシプロピルメチルジエトキシシラン β−(3,4-エポキシシクロヘキシル)エチルトリメトキ
シシラン β−(3,4-エポキシシクロヘキシル)エチルトリエトキ
シシラン γ−(メタ)アクリロキシプロピルトリメトキシシラン γ−(メタ)アクリロキシプロピルトリエトキシシラン γ−(メタ)アクリロキシプロピルメチルジメトキシシ
ラン γ−(メタ)アクリロキシプロピルメチルジエトキシシ
ラン γ−アミノプロピルトリメトキシシラン γ−アミノプロピルトリエトキシシラン γ−アミノプロピルメチルジメトキシシラン γ−アミノプロピルメチルジエトキシシラン γ−メルカプトプロピルトリメトキシシラン γ−メルカプトプロピルトリエトキシシラン ビニルトリクロルシシラン ビニルトリブロムシラン ビニルトリメトキシシラン ビニルトリエトキシシラン トリフルオロプロピルトリクロルシラン トリフルオロプロピルトリブロムシシラン トリフルオロプロピルトリメトキシシラン トリフルオロプロピルトリエトキシシラン およびこれらの部分加水分解物などが挙げられる。原料
の入手のしやすさ、扱いやすさから考えてジアルコキシ
シラン、トリアルコキシシラン、テトラアルコキシシラ
ンを用いるのが好ましい。Here, the silicone resin contains a hydrolyzed condensate of silane having 2 to 4 hydrolyzable groups. Examples of the hydrolyzable silane as the raw material are methyltrichlorosilane, methyltribromosilane, methyltrimethoxysilane, methyltriethoxysilane, methyltriisopropoxysilane, methyltri-t-butoxysilane, ethyltrichlorosilane, ethyltribromosilane, ethyltrimethoxysilane, and ethyl. Triethoxysilane ethyltriisopropoxysilane n-propyltrichlorosilane n-propyltribromosilane n-propyltrimethoxysilane n-propyltriethoxysilane n-propyltriisopropoxysilane n-hexyltrichlorosilane n-hexyltribromosilane n -Hexyltrimethoxysilane n-hexyltriethoxysilane n-decyltrimethoxysilane n-decyltriethoxysilane n-octa Syltrimethoxysilane n-octadecyltriethoxysilane Phenyltrichlorosilane Phenyltribromosilane Phenyltrimethoxysilane Phenyltriethoxysilane Tetrachlorosilane Tetrabromosilane Tetramethoxysilane Tetraethoxysilane Tetrabutoxysilane Dimethoxydiethoxysilane Dimethoxydiethoxysilane Dimethyldi Chlorosilane Dimethyldibromosilane Dimethyldimethoxysilane Dimethyldiethoxysilane Diphenyldichlorosilane Diphenyldibromosilane Diphenyldimethoxysilane Diphenyldiethoxysilane Phenylmethyldichlorosilane Phenylmethyldibromsilane Phenylmethyldimethoxysilane Phenylmethyldiethoxysilane Trichlorohydrosilane Tribromide Silane Trimethoxyhydrosilane Triethoxyhydrosilane γ-glycidoxypropyltrimethoxysilane γ-glycidoxypropyltriethoxysilane γ-glycidoxypropylmethyldimethoxysilane γ-glycidoxypropylmethyldiethoxysilane β- (3,4 -Epoxycyclohexyl) ethyltrimethoxysilane β- (3,4-epoxycyclohexyl) ethyltriethoxysilane γ- (meth) acryloxypropyltrimethoxysilane γ- (meth) acryloxypropyltriethoxysilane γ- (meth) acry Roxypropylmethyldimethoxysilane γ- (meth) acryloxypropylmethyldiethoxysilane γ-aminopropyltrimethoxysilane γ-aminopropyltriethoxysilane γ-aminopropylmethyldimethoxysilane γ-Aminopropylmethyldiethoxysilane γ-mercaptopropyltrimethoxysilane γ-mercaptopropyltriethoxysilane Vinyltrichlorosilane Silane Vinyltribromosilane Vinyltrimethoxysilane Vinyltriethoxysilane Trifluoropropyltrichlorosilane Trifluoropropyltribromosilane Tri Fluoropropyltrimethoxysilane Examples include trifluoropropyltriethoxysilane and partial hydrolysates thereof. It is preferable to use dialkoxysilane, trialkoxysilane, or tetraalkoxysilane from the viewpoint of easy availability and handling of the raw materials.
【0015】(2)上記親水性を維持しつつ、光触媒
(光酸化)反応をより強める方法としては以下を挙げる
ことができる。白金、パラジウム、ルテニウム、金、
銀、銅を部材表面層に添加し、固定する方法である。こ
れらの添加によって上記の効果がある理由は、光酸化反
応を促進するには、電子と正孔の再結合を防止しつつ、
正孔と水酸イオンとの反応により生成する水酸ラジカル
等の活性酸素を生成させる必要がある(これら活性酸素
が酸化反応に直接寄与するため)が、上記金属は電子を
有効に捕捉し再結合を生じさせない働きをするのであ
る。これらの働きをする金属には他に鉄、ニッケル、コ
バルトがあるが、これら金属はおそらく(ガス等の)吸
着性が大きすぎるため親水性を悪化させるものと思われ
る。(2) The following can be mentioned as a method of further enhancing the photocatalytic (photooxidation) reaction while maintaining the hydrophilicity. Platinum, palladium, ruthenium, gold,
In this method, silver and copper are added to the surface layer of the member and fixed. The reason why these additions have the above effect is to promote the photooxidation reaction while preventing recombination of electrons and holes.
Although it is necessary to generate active oxygen such as hydroxyl radicals generated by the reaction of holes and hydroxide ions (since these active oxygen contribute directly to the oxidation reaction), the above metal effectively traps electrons and regenerates them. It works to prevent binding. Other metals that perform these functions include iron, nickel, and cobalt, but these metals probably have too large an adsorptive property (gas, etc.) and thus deteriorate hydrophilicity.
【0016】本発明においては、上記光触媒含有層を、
光耐蝕性物質を介して基材表面に固定することができ
る。より強固に光触媒物質を基材上に固定できるからで
ある。ここでいう光耐蝕性物質の例としては、無機バイ
ンダー(無定型シリカ、水ガラス、釉薬等)、シリコー
ン樹脂、フッ素樹脂、アクリルシリコン等を挙げること
ができる。In the present invention, the photocatalyst containing layer is
It can be fixed to the surface of the substrate through a photocorrosion resistant material. This is because the photocatalytic substance can be more firmly fixed on the substrate. Examples of the photo-corrosion resistant substance include inorganic binders (amorphous silica, water glass, glaze, etc.), silicone resins, fluororesins, acrylic silicones, and the like.
【0017】本発明のフィルターの構造(形状)は、網
状、ハニカム状、多孔質板等公知のものを広く用いるこ
とができる。As the structure (shape) of the filter of the present invention, known ones such as mesh, honeycomb and porous plate can be widely used.
【0018】本発明における光触媒作用を有する部材の
基材としては、プラスチック、紙、金属、フィルム、塩
ビ鋼板、アルマイト処理アルミニウム、クロメート処理
金属、セラミックペーパー、ガラス繊維不織布等様々な
ものを限定なく使用できる。基材表面に活性炭等の大気
汚染物質吸着物質を担持し、その上にさらに光触媒含有
層を設けてもよい。さらに、フィルターの場合は、基材
そのものが活性炭製であってもよい。Various materials such as plastic, paper, metal, film, vinyl chloride steel plate, alumite-treated aluminum, chromate-treated metal, ceramic paper, and glass fiber non-woven fabric can be used without limitation as the base material of the member having a photocatalytic action in the present invention. it can. You may carry an air pollutant adsorption substance, such as activated carbon, on the surface of a base material, and further provide a photocatalyst containing layer on it. Further, in the case of a filter, the base material itself may be made of activated carbon.
【0019】[0019]
【実施例】以下、図及び実験例を参照しつつ、より具体
的に説明する。図1は、本発明の一実施例に係る大気汚
染物質除去用フィルターを有する換気扇の構成を示す模
式的断面図である。図1の換気扇1は、建屋壁3にはめ
込まれており、フィルター13、ファン15及び枠11
を備える。フィルター13は、換気扇1内の風の流路全
体に拡がるように設けられている。フィルター13は、
表面に光触媒含有層を有する通気性基材、具体的には後
述の実施例4として示す材料でできている。このフィル
ター13には屋外光が当り、上述の大気汚染物質除去機
能及び親水性を発揮する。したがって、雨水による自然
洗浄又は定期的な水洗いだけで、長期間にわたり大気汚
染物質除去機能を発揮する。EXAMPLES Hereinafter, more specific description will be given with reference to the drawings and experimental examples. FIG. 1 is a schematic cross-sectional view showing the configuration of a ventilation fan having an air pollutant removal filter according to an embodiment of the present invention. The ventilation fan 1 shown in FIG. 1 is fitted into a building wall 3, and includes a filter 13, a fan 15, and a frame 11.
Is provided. The filter 13 is provided so as to spread over the entire flow path of the air inside the ventilation fan 1. The filter 13 is
It is made of a breathable substrate having a photocatalyst-containing layer on its surface, specifically, the material shown as Example 4 described later. The filter 13 is exposed to outdoor light and exhibits the above-mentioned air pollutant removing function and hydrophilicity. Therefore, the air pollutant removal function can be exerted for a long period of time only by natural washing with rainwater or regular washing with water.
【0020】図2は、図1の換気扇の外枠をガラス製
(透明部材製)とした変形例の換気扇を示す模式的断面
図である。この場合も、フィルター13には屋外光が当
り、フィルターは光触媒作用に基づく大気汚染物質除去
機能を発揮する。図2の換気扇の方が屋外から見たとき
に見映えがよい。FIG. 2 is a schematic sectional view showing a modification of the ventilation fan of FIG. 1 in which the outer frame is made of glass (made of transparent material). Also in this case, the filter 13 is exposed to outdoor light, and the filter exerts an air pollutant removing function based on the photocatalytic action. The ventilation fan in FIG. 2 looks better when viewed from the outside.
【0021】図3は、光触媒作用を促す紫外線ランプを
有する換気扇の実施例の構成を模式的に示す断面図であ
る。すなわち、フィルター13とファン15の間に紫外
線ランプ21が設置されており、フィルター13に紫外
線が照射されて光触媒作用がより促進される。あるい
は、屋外光の当らない場所に設置される換気扇にも適用
できる。ここで、紫外線ランプ21の種類としては、B
LBランプ、水銀灯、メタルハライドランプ、キセノン
ランプ等を適用できる。FIG. 3 is a sectional view schematically showing the construction of an embodiment of a ventilation fan having an ultraviolet lamp for promoting a photocatalytic action. That is, the ultraviolet lamp 21 is installed between the filter 13 and the fan 15, and the filter 13 is irradiated with ultraviolet rays to further promote the photocatalytic action. Alternatively, it can be applied to a ventilation fan installed in a place where the outdoor light does not hit. Here, the type of the ultraviolet lamp 21 is B
An LB lamp, a mercury lamp, a metal halide lamp, a xenon lamp, etc. can be applied.
【0022】図4は、図3の換気扇の変形例で、紫外線
ランプの両側にフィルターを配置した換気扇を模式的に
示す断面図である。すなわち、紫外線ランプ21の上流
及び下流(図の左右)にはそれぞれフィルター13a、
13bが設けられている。両フィルター13a、13b
はそれぞれ紫外線ランプ21よりの紫外線照射を受け
る。フィルターが2重構造となっているため、大気汚染
物質の除去性が強化されている。FIG. 4 is a cross-sectional view schematically showing a modification of the ventilation fan of FIG. 3 in which filters are arranged on both sides of an ultraviolet lamp. That is, the filter 13a is provided upstream and downstream of the ultraviolet lamp 21 (on the left and right in the figure),
13b is provided. Both filters 13a, 13b
Each is irradiated with ultraviolet rays from the ultraviolet lamp 21. The double structure of the filter enhances the ability to remove air pollutants.
【0023】図5は、本発明の一実施例に係る大気汚染
物質除去機能を有するファンを備えた換気扇を示す図で
ある。(A)は全体の断面図、(B)はファン(シロッ
コファン)の斜視図である。この換気扇1−5はケーシ
ング33を有し、このケーシング33は、建屋壁13に
はめ込まれている。ケーシング33は、前面33a(外
側)が開放されているとともに下方に空気吹出し口33
bを有する。それらの開口には枠(格子)11が設けら
れている。FIG. 5 is a view showing a ventilation fan equipped with a fan having an air pollutant removing function according to an embodiment of the present invention. (A) is an overall sectional view, and (B) is a perspective view of a fan (sirocco fan). The ventilation fan 1-5 has a casing 33, and the casing 33 is fitted in the building wall 13. The front surface 33a (outside) of the casing 33 is open, and the air outlet 33 is opened downward.
b. A frame (lattice) 11 is provided in those openings.
【0024】ケーシング33内には、シロッコファン3
1が、その空気吸込み部(中心部)を外気側に向けて設
置されている。シロッコファン31は、建屋壁3に垂直
な軸方向に回転し、該軸方向に対して放射状に配置され
た多数の羽根32を有する。これらの羽根32は、表面
に光触媒含有層が形成された基材からなり、該表面の水
との接触角が5°未満である。具体的には、後述する実
施例3の部材からなる。羽根32の左右の端面には透明
部材からなる板34が貼られており、屋外光が羽根32
に当るようになっている。なお羽根32(翼)は全て平
板であり、音を静かにする効果がある。Inside the casing 33, the sirocco fan 3
1 is installed with its air suction portion (center portion) facing the outside air. The sirocco fan 31 rotates in an axial direction perpendicular to the building wall 3 and has a large number of blades 32 arranged radially with respect to the axial direction. These blades 32 are made of a base material having a photocatalyst-containing layer formed on the surface thereof, and the contact angle of the surface with water is less than 5 °. Specifically, it is composed of the members of Example 3 described later. Plates 34 made of a transparent material are attached to the left and right end surfaces of the blade 32 so that the outdoor light is exposed to the blade 32.
It is supposed to hit. The blades 32 (wings) are all flat plates and have the effect of quieting the sound.
【0025】シロッコファン31が回転すると、外気は
シロッコファン31の中心部が吸い込まれ、羽根32を
外周側に抜けて下方の空気吹出し口33bから室内に入
る。この羽根32を通過する際に、羽根32表面の光触
媒作用により、外気中の大気汚染物質が除去される。な
お、上述のように、羽根32には、透明板34を通して
屋外光が当る。When the sirocco fan 31 rotates, the outside air is sucked into the center of the sirocco fan 31, passes through the blades 32 to the outer peripheral side, and enters the room through the air outlet 33b below. When passing through the blade 32, air pollutants in the outside air are removed by the photocatalytic action of the surface of the blade 32. As described above, the vane 32 is exposed to the outdoor light through the transparent plate 34.
【0026】図6は、本発明の他の一実施例に係る大気
汚染物質除去用ファンの主要部を示す模式的斜視図であ
る。このシロッコファン31は、図5のシロッコファン
同様に、表面に光触媒含有層が形成された基材からなる
羽根32を具備する。さらに、その中心部に紫外線ラン
プ35を具備する。紫外線ランプ35から各羽根32に
紫外線が照射され、光触媒反応が促進される。FIG. 6 is a schematic perspective view showing a main part of an air pollutant removing fan according to another embodiment of the present invention. Similar to the sirocco fan of FIG. 5, the sirocco fan 31 includes blades 32 made of a base material having a photocatalyst containing layer formed on the surface thereof. Further, an ultraviolet lamp 35 is provided at the center thereof. Each blade 32 is irradiated with ultraviolet rays from the ultraviolet lamp 35 to accelerate the photocatalytic reaction.
【0027】[0027]
【実施例】以下、上述のフィルターやファンの羽根を形
成する材料の作製方法の具体例を述べる。以下の実施例
1〜5に係る試料及び比較例1、2に係る試料を準備し
た。実施例1 酸化チタンゾル(石原産業製STS11)と酸化スズゾ
ル(多木化学製、平均結晶子径3.5nm)を溶質重量比
85:15で混合した。この混合したものを15cm角の
ガラス不織布(三菱製紙製)に固形分重量で100mg塗
布し、150℃で10分焼成した。その後、塩化パラジ
ウム水溶液を塗布し、紫外線照射(条件0.5mW/cm2で
1分)でパラジウムを試料表面に光還元固定した。EXAMPLE A specific example of a method for producing a material for forming the above-mentioned filter or fan blade will be described below. Samples according to Examples 1 to 5 and Comparative Examples 1 and 2 below were prepared. Example 1 Titanium oxide sol (STS11 manufactured by Ishihara Sangyo) and tin oxide sol (manufactured by Taki Chemical Co., Ltd., average crystallite diameter 3.5 nm) were mixed at a solute weight ratio of 85:15. This mixed material was applied to a 15 cm-square glass non-woven fabric (made by Mitsubishi Paper Mills) at a solid content of 100 mg and baked at 150 ° C. for 10 minutes. After that, an aqueous palladium chloride solution was applied, and palladium was photoreduced and immobilized on the surface of the sample by irradiation with ultraviolet rays (condition: 0.5 mW / cm 2 for 1 minute).
【0028】実施例2 酸化チタンゾル(石原産業製STS11)とシリカゾル
(日産化学製、スノーテックス20)を溶質重量比8
0:20で混合した。この混合したものを15cm角のア
ルミナ−シリカ系セラミックペーパー(ニチアス製)に
固形分重量で100mg塗布し、500℃で10分焼成し
た。その後、ヘキサクロロ白金酸(IV)六水和物水溶液
を塗布し、紫外線照射(条件0.5mW/cm2で1分)で白
金を試料表面に光還元固定した。 Example 2 A solute weight ratio of titanium oxide sol (STS11 manufactured by Ishihara Sangyo) and silica sol (Snowtex 20 manufactured by Nissan Kagaku) was set to 8
Mixed at 0:20. This mixture was applied on a 15 cm-square alumina-silica ceramic paper (manufactured by Nichias Co., Ltd.) in a solid content of 100 mg and baked at 500 ° C. for 10 minutes. Then, an aqueous solution of hexachloroplatinic acid (IV) hexahydrate was applied, and platinum was photoreduced and immobilized on the surface of the sample by ultraviolet irradiation (condition: 0.5 mW / cm 2 for 1 minute).
【0029】実施例3 アクリル板上に、テトラエトキシシランを塗布し、15
0℃で加熱硬化し、無定型シリカ層を形成した。その
後、テトラエトキシシランと酸化チタンゾル(日産化学
製TA15)を、溶質重量比50:50で混合し、さら
にヘキサクロロ白金酸(IV)六水和物水溶液を、酸化チ
タン固形分に対する白金の量が2mol%となるように添加
した。この液状物をその上に塗布し、150℃で10分
焼成した。 Example 3 Tetraethoxysilane was coated on an acrylic plate, and 15
It was heat-cured at 0 ° C. to form an amorphous silica layer. Then, tetraethoxysilane and titanium oxide sol (TA15 manufactured by Nissan Chemical Industries, Ltd.) were mixed at a solute weight ratio of 50:50, and an aqueous solution of hexachloroplatinic acid (IV) hexahydrate was added, and the amount of platinum based on titanium oxide solid content was 2 mol. % Was added. This liquid material was applied onto it and baked at 150 ° C. for 10 minutes.
【0030】比較例1 アルミナ−シリカ系セラミックペーパー(ニチアス製)
に、酸化チタンゾル(石原産業製STS11)を固形分
重量で100mg塗布し、500℃で10分焼成した。そ
の後、塩化パラジウム水溶液を塗布し、紫外線照射(条
件0.5mW/cm2で1分)でパラジウムを試料表面に光還
元固定したものを準備した。 Comparative Example 1 Alumina-silica ceramic paper (Nichias)
Then, 100 mg of titanium oxide sol (STS11 manufactured by Ishihara Sangyo Co., Ltd.) was applied as a solid content weight, and baked at 500 ° C. for 10 minutes. Then, an aqueous palladium chloride solution was applied, and palladium was photoreduced and immobilized on the surface of the sample by irradiation with ultraviolet rays (condition: 0.5 mW / cm 2 for 1 minute) to prepare a sample.
【0031】実施例4 多孔質のアルミナ製セラミックペーパーに水ガラスを塗
布し、その後、酸化チタンゾル(多木化学製A6)とシ
リカゾル(日産化学製、スノーテックス20)とヘキサ
クロロ白金酸(IV)六水和物水溶液との混合液を塗布
し、500℃で焼成した。この試料のNOx 分解性及び
水洗浄性(詳細後述)は良好であった。 Example 4 Water glass was applied to a porous alumina ceramic paper, and then titanium oxide sol (A6 made by Taki Chemical Co., Ltd.), silica sol (Snowtex 20 made by Nissan Kagaku Co., Ltd.) and hexachloroplatinic acid (IV) hexahydrate were used. A mixed solution with an aqueous hydrate solution was applied and baked at 500 ° C. The NO x decomposability and water washability (described later in detail) of this sample were good.
【0032】比較例2 4フッ化エチレン樹脂粉末に酸化チタン光触媒粉末(デ
グサp−25)を重量比で6:4となるように機械的に
混合し、これを圧延して多孔質のシート状としたものを
作製した。この試料のNox分解性は良好であったが、
撥水性が高く水洗浄性はいずれの実施例よりも劣った。
なお水洗浄性とは油塗布後、水に試料を浸漬し、除去さ
れる程度を示す。 Comparative Example 2 Titanium dioxide photocatalyst powder (Degussa p-25) was mechanically mixed with tetrafluoroethylene resin powder in a weight ratio of 6: 4, and this was rolled to form a porous sheet. Was produced. Although the Nox decomposability of this sample was good,
The water repellency was high and the water washability was inferior to any of the examples.
The water washability means the degree to which the sample is removed by immersing the sample in water after applying the oil.
【0033】これらの試料に対して以下の項目を測定し
た。 水との接触角:接触角測定器(協和界面科学社製)によ
り水を約5μm 滴下後、30秒後に測定した。 水との接触角の維持性:1週間0.6mW/cm2のBLBラ
ンプ(紫外線照度は太陽光並)を照射し続けた後の水と
の接触角を測定した。The following items were measured for these samples. Contact angle with water: Measured with a contact angle measuring instrument (manufactured by Kyowa Interface Science Co., Ltd.) after dropping water by about 5 μm for 30 seconds. Maintainability of contact angle with water: The contact angle with water was measured after continuously irradiating a BLB lamp of 0.6 mW / cm 2 (ultraviolet illuminance was almost the same as sunlight) for one week.
【0034】気体分解率(S系ガス):メチルメルカプ
タンを11リットル容器に3ppm 入れ、0.6mW/cm2の
BLBランプを30分照射後の分解率を測定した。○は
70%以上、△は30〜70%、×は30%未満を示
す。 気体分解率(N系ガス):NO、NO2 混合ガス(N
O:NO2 =9:1)を11リットル容器に3ppm 入
れ、S系ガスの場合と同様に測定、評価した。Gas decomposition rate (S type gas): Methyl mercaptan was put into an 11 liter container at 3 ppm, and the decomposition rate was measured after irradiation with a 0.6 mW / cm 2 BLB lamp for 30 minutes. ◯ indicates 70% or more, Δ indicates 30 to 70%, and x indicates less than 30%. Gas decomposition rate (N-based gas): NO, NO 2 mixed gas (N
3 ppm of O: NO 2 = 9: 1) was placed in an 11-liter container, and the same measurement and evaluation as in the case of S-based gas were carried out.
【0035】疎水物質除去性:燃焼生成物の除去性を測
定した。具体的には、疎水性カーボンブラックを試料面
に噴射させ、水洗し、放置するサイクルを繰返したとき
の試料面の汚れ具合を観察した。○は汚れが目立たない
ことを示し、×は汚れが目立つことを示す。Hydrophobic substance removability: Removability of combustion products was measured. Specifically, the degree of soiling of the sample surface was observed when the cycle of spraying hydrophobic carbon black on the sample surface, washing with water, and leaving it was repeated. ○ indicates that the stain is not noticeable, and × indicates that the stain is noticeable.
【0036】親水物質除去性:無機質汚れの除去性を測
定した。具体的には、イエローオーカー含有物を分散し
た懸濁液を45°に傾斜させた試料面に流し、乾燥し、
水洗し、乾燥するサイクルを繰返したときの試料面の汚
れ具合を観察した。○は汚れが目立たないことを示し、
×は汚れが目立つことを示す。Removability of hydrophilic substances: Removability of inorganic stains was measured. Specifically, a suspension in which the yellow ocher-containing material is dispersed is poured onto a sample surface inclined at 45 °, dried,
When the cycle of washing with water and drying was repeated, the degree of contamination on the sample surface was observed. ○ indicates that dirt is not noticeable,
X indicates that the stain is conspicuous.
【0037】測定結果をまとめて表1に示す。The measurement results are summarized in Table 1.
【0038】[0038]
【表1】 [Table 1]
【0039】表1から分るように、各実施例とも、水と
の接触角は0°できわめて高い親水性を示した。さら
に、この親水性は1週間の紫外線照射後も高いまま維持
された。一方、各比較例は、水との接触角が5°以上で
あった。As can be seen from Table 1, in each of the examples, the contact angle with water was 0 °, which showed extremely high hydrophilicity. Furthermore, this hydrophilicity remained high even after 1 week of UV irradiation. On the other hand, in each comparative example, the contact angle with water was 5 ° or more.
【0040】気体(メチルメルカプタン)及びNO、N
O2 混合ガスの分解率については、実施例及び酸化チタ
ンを含む比較例1、2はいずれも良好であった。疎水物
質除去性は、各実施例及び比較的親水性の比較例1は良
好であった。しかし、比較的疎水性の比較例2は不良で
あった。親水物質除去性は、各実施例及び比較的疎水性
の比較例2は良好であった。しかし、比較的親水性の比
較例1は不良であった。Gas (methyl mercaptan) and NO, N
Regarding the decomposition rate of the O 2 mixed gas, the examples and the comparative examples 1 and 2 containing titanium oxide were good. The hydrophobic substance removability was good in each Example and Comparative Example 1 which was relatively hydrophilic. However, Comparative Example 2 which was relatively hydrophobic was poor. The hydrophilic substance removability was good in each Example and Comparative Example 2 which was relatively hydrophobic. However, Comparative Example 1, which was relatively hydrophilic, was poor.
【0041】「水と接触角5°未満」が本発明の条件で
あるが、この根拠となる実験例(実施例5)を以下に説
明する。実施例5 アナターゼ型チタニアゾル(STS−11)とコロイダ
ルシリカゾル(スノーテックス20)との混合物(固形
分におけるシリカの割合が10重量%)を固形分換算で
4.5mgだけ15cm四角のアルミナセラミック板(日本
カーバイド製)に塗布し、880℃の温度で10分焼成
した。その後、銅濃度50μmol/g の酢酸銅1水塩の水
溶液を0.3gスプレーコーティング法により塗布した
後乾燥させ、BLB蛍光灯により0.4mW/cm2の紫外線
照度で紫外線を10分間照射して酢酸銅1水塩を光還元
析出させることにより試料を得た。The condition of the present invention is "contact angle with water is less than 5 °", and an experimental example (Example 5) which is the basis for this is described below. Example 5 A mixture of anatase-type titania sol (STS-11) and colloidal silica sol (Snowtex 20) (the silica content in the solid content is 10% by weight) is 4.5 mg in terms of the solid content and a 15 cm square alumina ceramic plate ( (Made by Nippon Carbide) and baked at a temperature of 880 ° C. for 10 minutes. After that, 0.3 g of an aqueous solution of copper acetate monohydrate having a copper concentration of 50 μmol / g was applied by a spray coating method and then dried, and an ultraviolet ray was irradiated by a BLB fluorescent lamp at an ultraviolet illuminance of 0.4 mW / cm 2 for 10 minutes. A sample was obtained by photoreductive precipitation of copper acetate monohydrate.
【0042】この試料の水との接触角は4.0°であっ
た。次に、この試料について以下に示す汚泥試験(親水
性汚れ試験)を行った。まず、イエローオーカー64.
3重量%、焼成関東ローム粘土21.4重量%、疎水性
カーボンブラック4.8重量%、シリカ粉4.8重量
%、親水性カーボンブラック4.7重量%を1.05g
/リットルの濃度で水に懸濁させたスラリーを調整し
た。つぎに、45度に傾斜させた試料及び施釉タイル
(AB02E01)(比較例)に上記スラリー150ml
を流下させて15分間乾燥させ、次いで蒸留水150ml
を流下させて15分間乾燥させ、このサイクルを25回
反復した。試験前後の色差変化と光沢度変化を調べた。
光沢度の測定は日本工業規格(JIS)Z8741の規
定に従って行い、光沢度変化は試験後の光沢度を試験前
の光沢度で割ることにより求めた。The contact angle of this sample with water was 4.0 °. Next, the sludge test (hydrophilic stain test) shown below was performed on this sample. First, yellow ocher 64.
1.05 g of 3% by weight, calcined Kanto loam clay 21.4% by weight, hydrophobic carbon black 4.8% by weight, silica powder 4.8% by weight, hydrophilic carbon black 4.7% by weight
A slurry suspended in water at a concentration of 1 / liter was prepared. Next, 150 ml of the above slurry was applied to a sample tilted at 45 degrees and a glazed tile (AB02E01) (comparative example).
To dry for 15 minutes, then 150 ml of distilled water
And allowed to dry for 15 minutes and this cycle was repeated 25 times. The change in color difference and the change in gloss before and after the test were examined.
The glossiness was measured according to Japanese Industrial Standard (JIS) Z8741 and the change in glossiness was obtained by dividing the glossiness after the test by the glossiness before the test.
【0043】汚泥試験の結果は、本実施例の試料は色差
変化2.0、光沢度変化81.5%と、良好であった。
一方、比較例のアルミナセラミック板については、水と
の接触角19.4°、色差変化4.6、光沢度変化6
8.3%と不良であった。したがって、水との接触角5
°未満で、親水性汚れを効果的に除去できる超親水性表
面が得られるとの結論を得た。As a result of the sludge test, the sample of this example showed a favorable change in color difference of 2.0 and a change in glossiness of 81.5%.
On the other hand, regarding the alumina ceramic plate of the comparative example, the contact angle with water was 19.4 °, the color difference change was 4.6, and the gloss change was 6
It was a poor 8.3%. Therefore, the contact angle with water is 5
It was concluded that at less than °, a superhydrophilic surface is obtained that can effectively remove hydrophilic stains.
【0044】[0044]
【発明の効果】以上の説明から明らかなように、本発明
は、光触媒作用により大気汚染物質を反応させて捕捉で
きるとともに、フィルターやファン表面に付着した化学
反応生成物も水洗いによって容易に洗浄除去できるの
で、被対象物質を長期にわたって有効に除去しうる大気
汚染物質除去用フィルター、大気汚染物質除去用ファン
又は換気装置を提供できる。As is apparent from the above description, according to the present invention, air pollutants can be reacted and captured by a photocatalytic action, and chemical reaction products adhering to the surfaces of filters and fans can be easily washed and removed by washing with water. Therefore, it is possible to provide an air pollutant removal filter, an air pollutant removal fan or a ventilation device capable of effectively removing a target substance for a long period of time.
【図1】本発明の一実施例に係る大気汚染物質除去用フ
ィルターを有する換気扇の構成を示す模式的断面図であ
る。FIG. 1 is a schematic cross-sectional view showing the configuration of a ventilation fan having an air pollutant removal filter according to an embodiment of the present invention.
【図2】図1の換気扇の外枠をガラス製(透明部材製)
とした変形例の換気扇を示す模式的断面図である。2] The outer frame of the ventilation fan in FIG. 1 is made of glass (made of transparent material).
It is a typical sectional view showing the ventilation fan of a modification.
【図3】光触媒作用を促す紫外線ランプを有する換気扇
の実施例の構成を模式的に示す断面図である。FIG. 3 is a cross-sectional view schematically showing the configuration of an example of a ventilation fan having an ultraviolet lamp that promotes a photocatalytic action.
【図4】図3の換気扇の変形例で、紫外線ランプの両側
にフィルターを配置した換気扇を模式的に示す断面図で
ある。FIG. 4 is a cross-sectional view schematically showing a ventilation fan in which filters are arranged on both sides of an ultraviolet lamp, which is a modification of the ventilation fan of FIG.
【図5】本発明の一実施例に係る大気汚染物質除去機能
を有するファンを備えた換気扇を示す図である。(A)
は全体の断面図、(B)はファン(シロッコファン)の
斜視図である。FIG. 5 is a diagram showing a ventilation fan including a fan having an air pollutant removing function according to an embodiment of the present invention. (A)
Is a sectional view of the whole, and (B) is a perspective view of a fan (sirocco fan).
【図6】本発明の他の一実施例に係る大気汚染物質除去
用ファンの主要部を示す模式的斜視図である。FIG. 6 is a schematic perspective view showing a main part of an air pollutant removal fan according to another embodiment of the present invention.
【図7】部材表面付着物質の性質と、部材表面の水との
接触角との関係を示すグラフである。FIG. 7 is a graph showing the relationship between the property of the substance adhering to the member surface and the contact angle of the member surface with water.
1 換気扇 3 建屋壁 11 枠 13 フィルター 15 ファン 19 ガラス 21 紫外線ランプ 31 シロッコファン 32 羽根 33 ケーシング 33a 前面 33b 空気吹出し口 34 透明板 35 紫外線ランプ 1 Ventilation Fan 3 Building Wall 11 Frame 13 Filter 15 Fan 19 Glass 21 UV Lamp 31 Sirocco Fan 32 Blades 33 Casing 33a Front 33b Air Outlet 34 Transparent Plate 35 UV Lamp
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B01J 23/14 B01D 53/36 J 23/62 102B 35/02 ZAB 102E ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display location B01J 23/14 B01D 53/36 J 23/62 102B 35/02 ZAB 102E
Claims (10)
の基材からなり、 該表面は、水との接触角が5°未満の親水性であること
を特徴とする大気汚染物質除去用フィルター。1. An air pollutant for removing air pollutants, comprising a gas-permeable base material having a photocatalyst-containing layer formed on the surface, the surface being hydrophilic with a contact angle with water of less than 5 °. filter.
らなる羽根を有し、 該表面の水との接触角が5°未満の親水性であることを
特徴とする大気汚染物質除去用ファン。2. For removing air pollutants, which has a blade made of a base material having a photocatalyst-containing layer formed on the surface thereof, and is hydrophilic with a contact angle of water on the surface of less than 5 °. fan.
用フィルター及び/又は大気汚染物質除去用ファンを有
し、 該フィルター及び/又はファンが屋外光の照射を受けう
る状態に配置されていることを特徴とする換気装置。3. The filter for removing air pollutants and / or the fan for removing air pollutants according to claim 1 or 2, wherein the filter and / or the fan are arranged in a state where they can be irradiated with outdoor light. Ventilation device characterized by being.
用フィルター及び/又は大気汚染物質除去用ファンと、 該フィルター及び/又はファンに紫外線を照射する手段
と、を有することを特徴とする換気装置。4. An air pollutant removal filter and / or an air pollutant removal fan according to claim 1 or 2, and means for irradiating the filter and / or fan with ultraviolet rays. Ventilation equipment.
親水性である請求項1〜4いずれか1項記載の大気汚染
物質除去用フィルター、大気汚染物質除去用ファン又は
換気装置。5. The filter for removing air pollutants, the fan for removing air pollutants, or the ventilation device according to claim 1, wherein the surface is hydrophilic with a contact angle with water of approximately 0 °. .
ズを主成分とする物質からなる請求項1〜5いずれか1
項記載の大気汚染物質除去用フィルター、大気汚染物質
除去用ファン又は換気装置。6. The outermost surface of the member is made of a substance containing titanium oxide and tin oxide as main components.
A filter for removing air pollutants, a fan for removing air pollutants, or a ventilator according to the above item.
イ素を主成分とする物質からなる請求項1〜5いずれか
1項記載の大気汚染物質除去用フィルター、大気汚染物
質除去用ファン又は換気装置。7. The air pollutant removing filter, the air pollutant removing fan or the ventilation according to claim 1, wherein the outermost surface of the member is made of a substance containing titanium oxide and silicon oxide as main components. apparatus.
コーン樹脂を主成分とする物質からなり、かつその最表
面は酸化チタンとポリヒドロキシシロキサンを主成分と
する物質からなる請求項1〜5いずれか1項記載の大気
汚染物質除去用フィルター、大気汚染物質除去用ファン
又は換気装置。8. The surface layer of the member is made of a material containing titanium oxide and silicone resin as main components, and the outermost surface thereof is made of a material containing titanium oxide and polyhydroxysiloxane as main components. The filter for removing air pollutants, the fan for removing air pollutants, or the ventilation device according to any one of claims 1.
金、パラジウム、ルテニウム、金及び銀の内の少なくと
も1種が添加されている請求項1〜5いずれか1項記載
の大気汚染物質除去用フィルター、大気汚染物質除去用
ファン又は換気装置。9. The air pollutant according to claim 1, wherein at least one of platinum, palladium, ruthenium, gold and silver is added to the substance forming the surface layer of the member. Removal filter, air pollutant removal fan or ventilation system.
介して基材表面に固定されている請求項1〜9いずれか
1項記載の大気汚染物質除去用フィルター、大気汚染物
質除去用ファン又は換気装置。10. The filter for removing air pollutants and the fan for removing air pollutants according to claim 1, wherein the photocatalyst-containing layer is fixed to the surface of the base material via a photocorrosion resistant substance. Or a ventilation system.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8150410A JPH09225263A (en) | 1995-12-22 | 1996-05-23 | Air pollutant removing filter, air pollutant removing fan and ventilator using the fan |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7-354649 | 1995-12-22 | ||
| JP35464995 | 1995-12-22 | ||
| JP8150410A JPH09225263A (en) | 1995-12-22 | 1996-05-23 | Air pollutant removing filter, air pollutant removing fan and ventilator using the fan |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09225263A true JPH09225263A (en) | 1997-09-02 |
Family
ID=93155489
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8150410A Pending JPH09225263A (en) | 1995-12-22 | 1996-05-23 | Air pollutant removing filter, air pollutant removing fan and ventilator using the fan |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH09225263A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09230105A (en) * | 1995-12-22 | 1997-09-05 | Toto Ltd | Antifogging method and facility applied with the method |
| JP2000220860A (en) * | 1999-01-28 | 2000-08-08 | Sharp Corp | Air conditioner |
| JP2000334308A (en) * | 1999-05-25 | 2000-12-05 | Shinichi Harigai | Cafrrier for photocatalyst and photocatalyst using the same |
| JP2000334309A (en) * | 1999-05-25 | 2000-12-05 | Shinichi Harigai | Photocatalyst |
| JP2001000814A (en) * | 1999-06-21 | 2001-01-09 | Matsushita Electric Ind Co Ltd | air purifier |
-
1996
- 1996-05-23 JP JP8150410A patent/JPH09225263A/en active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09230105A (en) * | 1995-12-22 | 1997-09-05 | Toto Ltd | Antifogging method and facility applied with the method |
| JP2000220860A (en) * | 1999-01-28 | 2000-08-08 | Sharp Corp | Air conditioner |
| JP2000334308A (en) * | 1999-05-25 | 2000-12-05 | Shinichi Harigai | Cafrrier for photocatalyst and photocatalyst using the same |
| JP2000334309A (en) * | 1999-05-25 | 2000-12-05 | Shinichi Harigai | Photocatalyst |
| JP2001000814A (en) * | 1999-06-21 | 2001-01-09 | Matsushita Electric Ind Co Ltd | air purifier |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1917950A (en) | Bifunctional layered photocatalyst/thermocatalyst for improving indoor air quality | |
| JP6726313B2 (en) | Photocatalytic functional filter | |
| RU2151632C1 (en) | Photocatalytic element and method for manufacture thereof | |
| CN115279487A (en) | Method for manufacturing a photocatalytic device, photocatalytic composition and gas decontamination apparatus | |
| JP2004283646A (en) | Photocatalyst and method for producing photocatalyst | |
| JP2945926B2 (en) | Photocatalyst particles and method for producing the same | |
| JPH09225263A (en) | Air pollutant removing filter, air pollutant removing fan and ventilator using the fan | |
| JP2005254128A (en) | Photocatalyst particles, immobilization method thereof, and photocatalytic member | |
| JPH0978665A (en) | Toilet bowl | |
| JP4635185B2 (en) | Photocatalytic coating method for polyester fiber | |
| JPH09239277A (en) | Photocatalytic powder, photocatalyst using the powder and environment cleaning method using them | |
| RU2482912C1 (en) | Method of producing filtering-sorbing material with photo catalytic properties | |
| JP5245150B2 (en) | Photocatalyst coating method for polyester molding | |
| CN205019962U (en) | Photocatalytic filter | |
| JP3661814B2 (en) | Membrane structure material and cleaning method thereof | |
| JP2003268945A (en) | Interior finish material | |
| JP2003103142A (en) | Gas cleaning device | |
| JPH09271731A (en) | Removing method of objective material | |
| US11565246B2 (en) | Photocatalytic filter, method for manufacturing the same, and method for reactivating the same | |
| JP3115534B2 (en) | Inner wall of antifouling tunnel, antifouling method and cleaning method | |
| JPH0978462A (en) | Hydrophilic fiber and its processed product | |
| JP4190762B2 (en) | Method for producing gas processing material having excellent CO removal capability | |
| JP3534072B2 (en) | Bathroom components | |
| JP3189682B2 (en) | Antifouling material | |
| JP2001087629A (en) | N-based or s-based gas removing member |