JPH02251430A - Metal parts for gas heater, preparation thereof and gas heater - Google Patents
Metal parts for gas heater, preparation thereof and gas heaterInfo
- Publication number
- JPH02251430A JPH02251430A JP7362089A JP7362089A JPH02251430A JP H02251430 A JPH02251430 A JP H02251430A JP 7362089 A JP7362089 A JP 7362089A JP 7362089 A JP7362089 A JP 7362089A JP H02251430 A JPH02251430 A JP H02251430A
- Authority
- JP
- Japan
- Prior art keywords
- liquid composition
- sol
- forming
- ceramic layer
- raw materials
- 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
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 33
- 239000002184 metal Substances 0.000 title claims abstract description 33
- 239000000919 ceramic Substances 0.000 claims abstract description 71
- 239000000203 mixture Substances 0.000 claims abstract description 42
- 239000007788 liquid Substances 0.000 claims abstract description 38
- 239000002994 raw material Substances 0.000 claims abstract description 26
- 238000003980 solgel method Methods 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000000379 polymerizing effect Effects 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 10
- 239000000843 powder Substances 0.000 abstract description 10
- 239000000126 substance Substances 0.000 abstract description 8
- 230000007797 corrosion Effects 0.000 abstract description 3
- 238000005260 corrosion Methods 0.000 abstract description 3
- 150000004703 alkoxides Chemical class 0.000 abstract description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 abstract description 2
- 150000004692 metal hydroxides Chemical class 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 40
- 239000007789 gas Substances 0.000 description 38
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
- 238000010438 heat treatment Methods 0.000 description 13
- -1 t- Butyl Chemical group 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000000576 coating method Methods 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 239000000049 pigment Substances 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 239000011572 manganese Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 238000002845 discoloration Methods 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 239000010935 stainless steel Substances 0.000 description 5
- 229910001220 stainless steel Inorganic materials 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000010941 cobalt Substances 0.000 description 4
- 229910017052 cobalt Inorganic materials 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000008119 colloidal silica Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 210000003298 dental enamel Anatomy 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 235000019439 ethyl acetate Nutrition 0.000 description 3
- 238000001879 gelation Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000012779 reinforcing material Substances 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- LTPBRCUWZOMYOC-UHFFFAOYSA-N Beryllium oxide Chemical compound O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- AUNAPVYQLLNFOI-UHFFFAOYSA-L [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O Chemical compound [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O AUNAPVYQLLNFOI-UHFFFAOYSA-L 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 238000007590 electrostatic spraying Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- QSLPNSWXUQHVLP-UHFFFAOYSA-N $l^{1}-sulfanylmethane Chemical compound [S]C QSLPNSWXUQHVLP-UHFFFAOYSA-N 0.000 description 1
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 description 1
- IVORCBKUUYGUOL-UHFFFAOYSA-N 1-ethynyl-2,4-dimethoxybenzene Chemical compound COC1=CC=C(C#C)C(OC)=C1 IVORCBKUUYGUOL-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- VVLAIYIMMFWRFW-UHFFFAOYSA-N 2-hydroxyethylazanium;acetate Chemical compound CC(O)=O.NCCO VVLAIYIMMFWRFW-UHFFFAOYSA-N 0.000 description 1
- 241000722947 Acanthocybium Species 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- GRFKUEDWLAGOJX-UHFFFAOYSA-N acetic acid;butyl acetate Chemical class CC(O)=O.CCCCOC(C)=O GRFKUEDWLAGOJX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- UHHXUPJJDHEMGX-UHFFFAOYSA-K azanium;manganese(3+);phosphonato phosphate Chemical compound [NH4+].[Mn+3].[O-]P([O-])(=O)OP([O-])([O-])=O UHHXUPJJDHEMGX-UHFFFAOYSA-K 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- FWYSSOIRLVHQNC-UHFFFAOYSA-M benzyl(trimethyl)azanium;acetate Chemical compound CC([O-])=O.C[N+](C)(C)CC1=CC=CC=C1 FWYSSOIRLVHQNC-UHFFFAOYSA-M 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 229910000152 cobalt phosphate Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000008162 cooking oil Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- QHNXEVRKFKHMRL-UHFFFAOYSA-N dimethylazanium;acetate Chemical compound CNC.CC(O)=O QHNXEVRKFKHMRL-UHFFFAOYSA-N 0.000 description 1
- OREAFAJWWJHCOT-UHFFFAOYSA-N dimethylmalonic acid Chemical compound OC(=O)C(C)(C)C(O)=O OREAFAJWWJHCOT-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
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- 239000002657 fibrous material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
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- 238000007654 immersion Methods 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000008960 ketchup Nutrition 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 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
- 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
- 239000011976 maleic acid Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- XEDVYYJRECCCNM-UHFFFAOYSA-N n,n-dimethylaniline;formic acid Chemical compound OC=O.CN(C)C1=CC=CC=C1 XEDVYYJRECCCNM-UHFFFAOYSA-N 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- UJRBOEBOIXOEQK-UHFFFAOYSA-N oxo(oxochromiooxy)chromium hydrate Chemical compound O.O=[Cr]O[Cr]=O UJRBOEBOIXOEQK-UHFFFAOYSA-N 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- WFIZEGIEIOHZCP-UHFFFAOYSA-M potassium formate Chemical compound [K+].[O-]C=O WFIZEGIEIOHZCP-UHFFFAOYSA-M 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000005368 silicate glass Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 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
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000013555 soy sauce Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-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
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 229910021512 zirconium (IV) hydroxide Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、ガスこんろ用金属部品、ガスこんろ用金属部
品の製造法、及びガスこんろに関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a metal part for a gas stove, a method for manufacturing a metal part for a gas stove, and a gas stove.
従来の技術及びその問題点
厨房用ガス調理機器であるガスこんろでは、外装部の材
料としては、従来、有機樹脂塗装鋼板、ステンレス鋼板
、ホーロー板等が用いられている。BACKGROUND OF THE INVENTION Conventional techniques and their problems Conventionally, organic resin-coated steel plates, stainless steel plates, enamel plates, and the like have been used as materials for the exterior of gas stoves, which are gas cooking appliances for kitchens.
しかしながら、有機樹脂塗装鋼板を用いる場合には、有
機樹脂塗装が熱により劣化変色するという問題点があり
、またステンレス鋼板を用いる場合には、油汚れが付着
した場合に除去し難いという欠点がある。また、ホーロ
ー板は、重量が重いためにガスこんろ自体が重くなり、
しかも皮膜が欠は易いという欠点がある。However, when using organic resin-coated steel sheets, there is a problem that the organic resin coating deteriorates and discolors due to heat, and when using stainless steel sheets, there is a problem that it is difficult to remove oil stains if they adhere. . In addition, since the enamel plate is heavy, the gas stove itself becomes heavy.
Moreover, it has the disadvantage that the film is easily chipped.
ガスこんろのバーナ一部分は、従来、鉄鋳物、ステンレ
ス、アルミニウムダイキャスト、銅合金等が使用されて
いるが、これらは、熱による変色や発錆により、外観の
劣化が生じ易いことや腐食により欠損部が生じ易いとい
う問題点がある。Conventionally, the burner part of gas stoves has been made of cast iron, stainless steel, die-cast aluminum, copper alloy, etc. However, these materials tend to deteriorate in appearance due to discoloration and rusting due to heat, and are susceptible to corrosion. There is a problem in that defective parts are likely to occur.
また、煮こぼれの受は皿としては、従来ホーロー製やス
テンレス製のものが用いられているが、煮汁等が付着し
た場合に、除去が困難であり、掃除に手間がかかるとい
う欠点がある。In addition, enamel or stainless steel plates have been conventionally used to catch boiled spills, but they have the disadvantage that if boiling liquid or the like gets on them, it is difficult to remove and it takes time and effort to clean.
問題点を解決するための手段
本発明者は、上記した如き問題点に鑑みて、ガスこんろ
を構成する各種金属部品について、耐熱性、耐食性、耐
汚染性、耐傷付性等の向上とともに、優れた美感を付与
すべく鋭意研究を重ねてきた。その結果、ガスこんろを
構成する金属部品に、ゾル−ゲル法によりセラミックス
層を形成することによって、所期の目的が達成されるこ
とを見出し、ここに本発明を完成するに至った。Means for Solving the Problems In view of the above-mentioned problems, the inventors of the present invention have improved the heat resistance, corrosion resistance, stain resistance, scratch resistance, etc. of the various metal parts that constitute the gas stove. We have carried out extensive research to give it an excellent sense of beauty. As a result, the inventors discovered that the desired objective could be achieved by forming a ceramic layer on the metal parts constituting the gas stove by the sol-gel method, and thus completed the present invention.
即ち、本発明は、以下に示すガスこんろ用金属部品、該
金属部品の製造法、及びガスこんろを提供するものであ
る。That is, the present invention provides a metal component for a gas stove, a method for manufacturing the metal component, and a gas stove as shown below.
■ ゾル−ゲル法により形成されたセラミックス層を有
するガスこんろ用金属部品。■ Metal parts for gas stoves that have a ceramic layer formed by the sol-gel method.
■ ガスこんろを構成する金属部品上に、セラミックス
形成用原料の液状組成物を塗布し、重合ゲル化させてセ
ラミックス層を形成することを特徴とするガスこんろ用
金属部品の製造法。■ A method for manufacturing metal parts for gas stoves, which comprises applying a liquid composition of raw materials for forming ceramics onto the metal parts constituting the gas stove, and polymerizing and gelling the composition to form a ceramic layer.
■ ゾル−ゲル法により形成されたセラミックス層を有
する金属部品を構成部品として有するガスこんろ。■ A gas stove whose components are metal parts with a ceramic layer formed by the sol-gel method.
本発明によりセラミックス層を形成する対象となる材料
は、ガスこんろを構成する各種金属部品であり、例えば
、外装カバー、ガスバーナー、バーナーヘッド、受皿、
ごとく等を例示できる。これらの部品の材質は、特に限
定はなく、例えば鉄、アルミニウム、銅、ステンレス等
の各種の金属、又はこれらの合金等の他、亜鉛メツキ、
ニッケルメッキ、クロムメツキ、アルミニウムメツキ等
やその他各種金属メツキを施した材料も用いることがで
きる。The materials on which the ceramic layer is formed according to the present invention are various metal parts that constitute a gas stove, such as an exterior cover, a gas burner, a burner head, a saucer,
I can give examples such as ``Gotoku''. The materials of these parts are not particularly limited, and include various metals such as iron, aluminum, copper, stainless steel, and alloys thereof, as well as galvanized,
Materials plated with nickel plating, chrome plating, aluminum plating, or various other metals can also be used.
本発明のガスこんろ用金属部品は、上記した様な各種の
ガスこんろ構成材料上に、ゾル−ゲル法によるセラミッ
クス層を形成することによって得られる。The metal parts for gas stoves of the present invention can be obtained by forming a ceramic layer by a sol-gel method on various gas stove constituent materials as described above.
ゾル−ゲル法によるセラミックス層形成法としては、各
種の方法が公知であり、また、原料としても各種のもの
が知られているが、本発明では、これらは特に限定的で
はなく、いずれも採用できる。Various methods are known for forming ceramic layers using the sol-gel method, and various raw materials are also known, but in the present invention, these are not particularly limited, and any of them may be adopted. can.
ゾル−ゲル法によるセラミックスは、通常、セラミック
ス形成用原料の液状組成物を塗布し、重合、ゲル化させ
ることによって形成することができる。該液状組成物は
、各種の金属アルコキシドや金属ヒドロキシドをセラミ
ックス形成用原料として含有するものであり、この様な
セラミックス形成用原料の好ましい例として、
0式(R1) mMl (OR2) n(式中、R1は
炭素数1〜3のアルキル基又はビニル基、R2は水素、
メチル、エチル、イソプロピル又はt−ブチル、M、は
Ca又はBa。Ceramics produced by the sol-gel method can usually be formed by applying a liquid composition of ceramic-forming raw materials and polymerizing and gelling the composition. The liquid composition contains various metal alkoxides and metal hydroxides as raw materials for forming ceramics, and as a preferable example of such raw materials for forming ceramics, 0 formula (R1) mMl (OR2) n (formula Among them, R1 is an alkyl group or vinyl group having 1 to 3 carbon atoms, R2 is hydrogen,
Methyl, ethyl, isopropyl or t-butyl, M is Ca or Ba.
mは0又は1、nは1又は2を示す)で表わされる化合
物、
0式(R3) kM2(OR4)ρ
(式中、R3は炭素数1〜3のアルキル基又はビニル基
、R4は水素、メチル、エチル、イソプロピル又はt−
ブチル、M2はA、l;)、Y又はLa5kは0又は1
、ρは2又は3を示す)で表わされる化合物、
0式(Rs ) i M3 (ORB ) j(式中、
R5は炭素数1〜3のアルキル基又はビニル基、R6は
水素、メチル、エチル、イソプロピル又はt−ブチル、
M3はTi、Zr。m is 0 or 1, n is 1 or 2), 0 formula (R3) kM2(OR4)ρ (wherein R3 is an alkyl group or vinyl group having 1 to 3 carbon atoms, R4 is hydrogen , methyl, ethyl, isopropyl or t-
Butyl, M2 is A, l;), Y or La5k is 0 or 1
, ρ represents 2 or 3), a compound represented by the formula (Rs ) i M3 (ORB ) j (wherein,
R5 is an alkyl group having 1 to 3 carbon atoms or a vinyl group, R6 is hydrogen, methyl, ethyl, isopropyl or t-butyl,
M3 is Ti, Zr.
Mn5Sn、SL又は5rSiは0又は1、jは3又は
4を示す)で表わされる化合物、等を挙げることができ
る。これらの化合物は1種又は2種以上組み合わせて用
いること々(でき、また2種以上が縮合しているものを
用いてもよい。Mn5Sn, SL or 5rSi represents 0 or 1, j represents 3 or 4), and the like. These compounds may be used alone or in combination of two or more, and two or more of them may be condensed.
上記セラミックス形成用原料の具体例としては、(a
(OCH3) 2 、Ca (OC2Hs ) 2、C
a(OC3H7)2.Ca(OCtH9)2−Ba (
OCH3)2 、Ba (OC2H5)2、Ba (O
Ca Hy ) 2 、Ba (OCa H9) 2、
Aρ(OCH3)3 、A、Q (OC2Hs )3、
Ai’(OC3H7)3、AΩ(OCa H9)3、C
H3AΩ(OCH3)2 、CH3AΩ(OC2H5)
2、CH3AΩ(OCa Hy )2 、CH3AΩ(
OCa H9)2、Ti (OCH3)a 、Ti (
OC2H5)4、Ti (OCa Hy )A 、T
i (OCa H9)4、CH3Ti (OCH3)
3、CH3Ti (OC2H5)3、CH3Ti (O
Ca Hy )3 、CH3Ti (OC4H9) 3
、C2H5Ti (OCH3)3、C2H5Ti (O
C2H5)3、C2H5Ti (OCa Hy )3
、C2H5Ti (OCa Hg)3、Si (O
CH3)4、Si (OC2H5)A、Si (OC
3H7)4% Si (OC4H9)4、CH3Si
(OCH3)3、CH3Si (OC2H5)3、CH
3SL (OCa Hy )3 、CH3Si (OC
a Hg)3、C2H5Si (OCH3)3、C2H
5St (OC2H5)3、C2H5S i (OCa
Hy ) 3、C2H5Si (OC4Hg)3、Z
r (OCH3)4、Zr (OC2H5) 4、Zr
(OCa Hy ) 4、Zr (OCAH9)4、
CH3Zr (OCH3)3、CH3Zr (OC2H
5)3、CH3Zr (OCa Hy)3、CH3Zr
(OCa Ho) 3 、C2H5Zr (OCH3
) 3、C2H5Zr (OC2H5) 3、
C2H5Z r (OCa Hy ) 3、C2H5Z
r (OC4H9)3、Y(OCH3)3、Y (OC
2H5) 3 、Y (OCa Hy ) 3、Y (
OCa Hg ) 3 、L a (OCH3) s、
La (OC2Hs ) 3 、La (OCa Hy
) 3、La (OCa Hg)3 、Mn (OC
H3)4、Mn (OC2H5) 4 、Mn (OC
a Hy ) 4、Mn (OCa Hg)4.3n
(OCH3)A、Sn (OC2Hs ) a 、Sn
(OCa Hy ) 4、Sn (OCa Hg )
a 、S r (OCH3) 4、Sr (OC2H
5)4 、Sr (OCa Hy )4、Sr (OC
4Hg)4、Ca (OH)2、Ba (OH)2、A
、Q (OH) 3、CH3AΩ(OH)2 、TL
(OH)4、CH3Ti (OH)3 、C2H5T
i (OH)3、S i (OH)a 、CH3S
i (OH) 3、C2H5S i (OH)3
、Zr (OH)4、CH3Zr (OH)3 、C
2H5Zr (OH)3、Y (OH)3 、La (
OH)3 、Mn (OH)4、Sn (OH) a
、S r (OH) 4等を挙げることができる。また
、これらの縮合物は、上記化合物の任意の組み合わせに
より自由に作製でき、分子量も適宜選択できる。縮合物
の一例としては、
Zr03i (OC2H5) 6 、A、QO8i (
OC2Hs ) s、TiO3i (OC2H5) s
、
(C3Hy 0) 3 Z rO3i (OC2H5)
3、(C4Hg O) 3 Z rO8i (OC2
H5) 3、(C3Hy 0) 3 TiO3i (O
C2Hs ) 3、(CムHg0)3TiO3i (
OC2H5)3、(C3Hy O)2 AρO3i
(OC2H5)3、(Ca H90)2 AΩO8i
(OC2Hs )3、等を示すことができる。Specific examples of the raw materials for forming ceramics include (a
(OCH3) 2, Ca (OC2Hs) 2, C
a(OC3H7)2. Ca(OCtH9)2-Ba (
OCH3)2, Ba (OC2H5)2, Ba (O
Ca Hy ) 2 , Ba (OCa H9) 2 ,
Aρ(OCH3)3, A,Q(OC2Hs)3,
Ai'(OC3H7)3, AΩ(OCa H9)3, C
H3AΩ(OCH3)2, CH3AΩ(OC2H5)
2, CH3AΩ(OCa Hy )2, CH3AΩ(
OCa H9)2, Ti (OCH3)a, Ti (
OC2H5)4, Ti (OCaHy)A, T
i (OCa H9)4, CH3Ti (OCH3)
3, CH3Ti (OC2H5)3, CH3Ti (O
Ca Hy ) 3 , CH3Ti (OC4H9) 3
, C2H5Ti (OCH3)3, C2H5Ti (O
C2H5)3, C2H5Ti (OCaHy)3
, C2H5Ti (OCa Hg)3, Si (O
CH3)4, Si (OC2H5)A, Si (OC
3H7)4% Si (OC4H9)4, CH3Si
(OCH3)3, CH3Si (OC2H5)3, CH
3SL (OCa Hy )3 , CH3Si (OC
a Hg)3, C2H5Si (OCH3)3, C2H
5St (OC2H5)3, C2H5S i (OCa
Hy ) 3, C2H5Si (OC4Hg)3, Z
r (OCH3)4, Zr (OC2H5) 4, Zr
(OCa Hy) 4, Zr (OCAH9) 4,
CH3Zr (OCH3)3, CH3Zr (OC2H
5) 3, CH3Zr (OCa Hy)3, CH3Zr
(OCa Ho) 3 , C2H5Zr (OCH3
) 3, C2H5Zr (OC2H5) 3, C2H5Z r (OCa Hy) 3, C2H5Z
r (OC4H9)3, Y(OCH3)3, Y (OC
2H5) 3, Y (OCa Hy) 3, Y (
OCa Hg) 3, L a (OCH3) s,
La (OC2Hs) 3, La (OCa Hy
) 3, La (OCa Hg)3, Mn (OC
H3) 4, Mn (OC2H5) 4, Mn (OC
a Hy ) 4, Mn (OCa Hg) 4.3n
(OCH3) A, Sn (OC2Hs) a, Sn
(OCa Hy) 4, Sn (OCa Hg)
a, S r (OCH3) 4, Sr (OC2H
5)4,Sr(OCaHy)4,Sr(OC
4Hg)4, Ca (OH)2, Ba (OH)2, A
,Q(OH)3,CH3AΩ(OH)2,TL
(OH)4, CH3Ti (OH)3, C2H5T
i (OH)3, S i (OH)a, CH3S
i (OH) 3, C2H5S i (OH)3
,Zr(OH)4,CH3Zr(OH)3,C
2H5Zr (OH)3, Y (OH)3, La (
OH)3, Mn (OH)4, Sn (OH) a
, S r (OH) 4 and the like. Moreover, these condensates can be freely produced by any combination of the above-mentioned compounds, and the molecular weight can also be selected as appropriate. Examples of condensates include Zr03i (OC2H5) 6 , A, QO8i (
OC2Hs ) s, TiO3i (OC2H5) s
, (C3Hy 0) 3 Z rO3i (OC2H5)
3, (C4Hg O) 3 Z rO8i (OC2
H5) 3, (C3Hy 0) 3 TiO3i (O
C2Hs) 3, (CmuHg0)3TiO3i (
OC2H5)3, (C3Hy O)2 AρO3i
(OC2H5)3, (Ca H90)2 AΩO8i
(OC2Hs)3, etc. can be shown.
これらのセラミックス形成用原料は、通常、有機溶剤、
水、これらの混合溶媒等に溶解又は分散して用いられる
が、セラミックス形成用原料自体で液状のものは、その
まま用いることも可能である。有機溶剤は、公知のゾル
−ゲル法の液状組成物において用いられるものをいずれ
も使用でき、例えば、メタノール、エタノール、プロパ
ツール、ブタノール等の低級アルコール類、エチレング
リコールモノアルキルエーテル、ジエチレングリコール
モノアルキルエーテル、プロピレングリコールモノアル
キルエーテル、ジプロピレングリコールモノアルキルエ
ーテル等のアルキル基としてメチル、エチル、プロピル
、ブチル等を有する炭化水素エーテルアルコール類、エ
チレングリコールモノアルキルエーテルアセテート、ジ
エチレングリコールモノアルキルエーテルアセテート、
プロピレングリコールモノアルキルエーテルアセテート
、ジプロピレングリコールモノアルキルエーテルアセテ
ート等の上記炭化水素エーテルアルコール類の酢酸エス
テル類、エトキシエチルアセテート等のアルコール類の
酢酸エステル類、酢酸メチル、酢酸エチル、酢酸プロピ
ル、酢酸ブチル等の酢酸エステル類、アセトン等を用い
ることができる。These raw materials for forming ceramics usually contain organic solvents,
It is used after being dissolved or dispersed in water, a mixed solvent thereof, etc., but if the raw material for forming ceramics itself is liquid, it is also possible to use it as it is. As the organic solvent, any one used in the liquid composition of the known sol-gel method can be used, such as lower alcohols such as methanol, ethanol, propatool, butanol, ethylene glycol monoalkyl ether, diethylene glycol monoalkyl ether, etc. , hydrocarbon ether alcohols having methyl, ethyl, propyl, butyl, etc. as an alkyl group such as propylene glycol monoalkyl ether, dipropylene glycol monoalkyl ether, ethylene glycol monoalkyl ether acetate, diethylene glycol monoalkyl ether acetate,
Acetate esters of the above hydrocarbon ether alcohols such as propylene glycol monoalkyl ether acetate and dipropylene glycol monoalkyl ether acetate, acetate esters of alcohols such as ethoxyethyl acetate, methyl acetate, ethyl acetate, propyl acetate, butyl acetate Acetate esters such as, acetone, etc. can be used.
液状組成物中のセラミックス形成用原料の濃度は、通常
10〜100重量%程度とすればよく、使用する原料の
性質に応じて適宜決定すればよい。The concentration of the raw material for forming ceramics in the liquid composition is usually about 10 to 100% by weight, and may be determined as appropriate depending on the properties of the raw material used.
また、上記セラミックス形成用原料の液状組成物には、
必要に応じてコロイド状物質及び/又は無機微粉末を添
加することができる。コロイド状物質及び/又は無機微
粉末の添加によって、ゾル−ゲル法により形成されるセ
ラミックス層がより緻密化される。In addition, the liquid composition of the raw material for forming ceramics includes:
Colloidal substances and/or inorganic fine powders can be added as necessary. By adding the colloidal substance and/or the inorganic fine powder, the ceramic layer formed by the sol-gel method is made more dense.
本発明で用いられるコロイド状物質とは、10〜100
00オングストロ一ム程度の液状又は固体の粒子が分散
媒中に分散しているものをいい、各種の公知のものが使
用できる。分散媒としては、通常、上記した低級アルコ
ール類、炭化水素エーテルアルコール類、これらの酢酸
エステル類等の有機溶剤や水が単独又は混合して用いら
れており、分散粒子の濃度は10〜60重曾%程度のも
のが一般的である。本発明では、このようなコロイド状
物質をいずれも用いることができる。コロイド状物質の
具体例としては、コロイド状シリカ、コロイド状アルミ
ナ、コロイド状酸化チタン、コロイド状酸化ジルコニウ
ム、コロイド状硅酸ジルコニウム、コロイド状水酸化ア
ルミニウム、コロイド状水酸化ジルコニウム等を挙げる
ことができる。The colloidal substance used in the present invention is 10 to 100
It refers to liquid or solid particles of about 0.00 angstroms dispersed in a dispersion medium, and various known types can be used. As the dispersion medium, organic solvents such as the above-mentioned lower alcohols, hydrocarbon ether alcohols, and acetic esters thereof, and water are used alone or in combination, and the concentration of the dispersed particles is 10 to 60% by weight. Generally, it is about 10%. In the present invention, any such colloidal substances can be used. Specific examples of colloidal substances include colloidal silica, colloidal alumina, colloidal titanium oxide, colloidal zirconium oxide, colloidal zirconium silicate, colloidal aluminum hydroxide, and colloidal zirconium hydroxide. .
無機微粉末は、粒子径5〜150mμ程度のものが適当
であり、例えばアルミナ微粉末、酸化チタン微粉末、シ
リカ微粉末等を用いることができる。The inorganic fine powder has a particle size of about 5 to 150 mμ, and for example, alumina fine powder, titanium oxide fine powder, silica fine powder, etc. can be used.
コロイド状物質及び/又は無機微粉末は、セラミックス
形成用原料の液状組成物中に70重量%程度まで添加す
ることができ、好ましくは、3〜40重量%程度添加す
ればよい。The colloidal substance and/or inorganic fine powder can be added up to about 70% by weight, preferably about 3 to 40% by weight, in the liquid composition of the raw material for forming ceramics.
上記セラミックス形成用原料の液状組成物には、更に必
要に応じて、顔料、被覆補強材等を添加してもよい。顔
料としては、通常の無機系、有機系の顔料を用いること
ができ、例えば、酸化マグネシウム、窒化硅素、窒化硼
素、窒化チタン、酸化ニッケル、石英、シリカ、硅酸ジ
ルコニウム、アルミナ、酸化チタン、チタンイエロー、
炭酸マグネシウム、ドロマイト、炭化硅素、炭化タング
ステン、酸化鉄(赤、黒)、バリウムイエロー、アンチ
モンイエロー、コバルトブルー、コバルトバイオレット
、コバルトグリーン、マンガンブラック、マンガンブル
ー、マンガンバイオレット、ストロンチウムクロメート
、タルク、クロムオキサイドハイドレートグリーン、ク
ロムオキサイドグリーン、亜鉛グリーン、炭酸バリウム
、チョーク、沈澱炭酸カルシウム、アルミニウムハイド
レート、酸化亜鉛、ホタル石、モリブデン赤、モリブデ
ンオレンジ、クロムイエロー、鉛クロメート、ウルトラ
マリーン、朱、塩基性炭酸鉛、アゾ系顔料等を用いるこ
とができる。顔料は、常法に従って顔料用充填剤、増粘
剤等とともに用いることができる。If necessary, a pigment, a coating reinforcing material, etc. may be added to the liquid composition of the raw material for forming ceramics. As the pigment, ordinary inorganic or organic pigments can be used, such as magnesium oxide, silicon nitride, boron nitride, titanium nitride, nickel oxide, quartz, silica, zirconium silicate, alumina, titanium oxide, and titanium. yellow,
Magnesium carbonate, dolomite, silicon carbide, tungsten carbide, iron oxide (red, black), barium yellow, antimony yellow, cobalt blue, cobalt violet, cobalt green, manganese black, manganese blue, manganese violet, strontium chromate, talc, chromium oxide Hydrate green, chromium oxide green, zinc green, barium carbonate, chalk, precipitated calcium carbonate, aluminum hydrate, zinc oxide, fluorite, molybdenum red, molybdenum orange, chrome yellow, lead chromate, ultramarine, vermilion, basic carbonate Lead, azo pigments, etc. can be used. Pigments can be used together with pigment fillers, thickeners, etc. in accordance with conventional methods.
被覆補強材は、無機質で繊維状のものをいい、この代表
例としてチタン酸カリウム、炭化硅素、窒化硅素、酸化
アルミニウム、ベリリア、炭化硼素、硅酸塩ガラス、石
英などがある。The coating reinforcing material is an inorganic fibrous material, and typical examples thereof include potassium titanate, silicon carbide, silicon nitride, aluminum oxide, beryllia, boron carbide, silicate glass, and quartz.
顔料は、液状組成物中に70重量%程度まで添加するこ
とができ、また被覆補強材は、液状組成物中に70重量
%程度まで、好ましくは1〜65重量%程度添加するこ
とができる。The pigment can be added to the liquid composition up to about 70% by weight, and the coating reinforcing material can be added to the liquid composition up to about 70% by weight, preferably about 1 to 65% by weight.
上記した液状組成物は、急速なゲル化を防止するために
pH2,5〜6.0程度に調整することが好ましい。p
H調整には、例えば、塩酸、酢酸、クロロ酢酸、クエン
酸、マレイン酸、シュウ酸、トルエンスルホン酸、グル
タル酸、ジメチルマロン酸、安息香酸等の無機酸又は有
機酸を用いることができる。The pH of the liquid composition described above is preferably adjusted to about 2.5 to 6.0 in order to prevent rapid gelation. p
For H adjustment, inorganic or organic acids such as hydrochloric acid, acetic acid, chloroacetic acid, citric acid, maleic acid, oxalic acid, toluenesulfonic acid, glutaric acid, dimethylmalonic acid, and benzoic acid can be used.
また、上記液状組成物には、更に、室温では該液状組成
物をゲル化させることがな(、加熱によって解離して該
液状組成物の重合を加速することのできる緩衝化潜触媒
として、カルボン酸金属塩、アミンカルボキシレート、
四級アンモニウムカルボキシレート、硝酸塩等を液状組
成物中に1,5重量%程度まで添加することができる。The liquid composition further contains carbon dioxide as a buffered latent catalyst that does not cause the liquid composition to gel at room temperature (and that can be dissociated by heating to accelerate the polymerization of the liquid composition). acid metal salts, amine carboxylates,
Quaternary ammonium carboxylate, nitrate, etc. can be added to the liquid composition up to about 1.5% by weight.
このような緩衝化潜触媒としては、ジメチルアミンアセ
テート、エタノールアミンアセテート、ジメチルアニリ
ンホルメート、酢酸ナトリウム、プロピオン酸ナトリウ
ム、ギ酸カリウム、ギ酸ナトリウム、ベンジルトリメチ
ルアンモニウムアセテート、硝酸ナトリウム、硝酸アン
モニウム等を例示できる。Examples of such buffered latent catalysts include dimethylamine acetate, ethanolamine acetate, dimethylaniline formate, sodium acetate, sodium propionate, potassium formate, sodium formate, benzyltrimethylammonium acetate, sodium nitrate, and ammonium nitrate.
また、セラミックス皮膜に柔軟性を付与したい場合、厚
塗りを可能にしたい場合等には、液状組成物中に、樹脂
変性シリコーンレジンを配合することができる。シリコ
ーンレジンの配合によって、セラミックス皮膜の柔軟性
が向上し、また樹脂変性したものを用いることによって
、プラスチックス素材との良好な密着性が保たれる。樹
脂変性の種類としては、例えばエポキシ変性、ポリエス
テル−アルキド変性、フェノール変性、アクリル変性な
どが挙げられる。樹脂変性シリコーンレジンとしては、
セラミックス形成用原料の液状組成物に可溶性のもので
あれば限定なく用いることができ、配合量は、液状組成
物中に、70重量%程度以下、好ましくは5〜50重量
%重量%型ればよい。Furthermore, when it is desired to impart flexibility to the ceramic film or to enable thick coating, a resin-modified silicone resin can be blended into the liquid composition. By blending silicone resin, the flexibility of the ceramic film is improved, and by using a resin-modified film, good adhesion to plastic materials can be maintained. Examples of types of resin modification include epoxy modification, polyester-alkyd modification, phenol modification, and acrylic modification. As a resin-modified silicone resin,
Any material can be used without limitation as long as it is soluble in the liquid composition of the raw material for forming ceramics. good.
本発明では、上記したセラミックス形成用原料の液状組
成物を、基材であるガスこんろ用金属部品上に、塗布し
、重合ゲル化させることによって、セラミックス層を形
成させる。セラミックス層を設ける部分は、各金属部品
の用途に応じた要求される部分のみで充分であり、例え
ば外装カバーでは表面部分、受は皿では上面部分、バー
ナーでは外部、などにセラミックス層を設けることによ
って、所期の目的を達成することができる。バーナーヘ
ッドやごとくでは通常、全面にセラミックス層が設けら
れる。In the present invention, a ceramic layer is formed by applying the above-described liquid composition of raw materials for forming ceramics onto a metal component for a gas stove, which is a base material, and polymerizing and gelling the composition. It is sufficient to provide the ceramic layer only on the required parts depending on the purpose of each metal part.For example, it is sufficient to provide the ceramic layer on the surface of the outer cover, the top surface of the tray, the outside of the burner, etc. By doing so, the intended purpose can be achieved. Burner heads and the like are usually provided with a ceramic layer over the entire surface.
塗布方法は特に限定はなく、例えば、スプレー法、ロー
ルコート法、デイツプ法、カーテンフロー法、印刷法等
を採用することができる。液状組成物の重合、ゲル化は
、常温でも進行するが、加熱することによって、ゲル化
時間が短縮され、また、重合密度が上がって、セラミッ
クス層がより緻密化する。加熱温度は、高温とするほど
セラミックス層をより緻密化することができるが、コス
ト面からは100〜250℃程度で10〜30分程度加
熱することが適当である。The coating method is not particularly limited, and for example, a spray method, a roll coating method, a dip method, a curtain flow method, a printing method, etc. can be employed. Polymerization and gelation of the liquid composition proceed even at room temperature, but heating shortens the gelation time and increases the polymerization density, making the ceramic layer more dense. The higher the heating temperature, the more dense the ceramic layer can be, but from a cost standpoint, heating at about 100 to 250° C. for about 10 to 30 minutes is appropriate.
尚、セラミックス層におけるピンホールの発生を完全に
防止するために、セラミックス形成用原料の液状組成物
の塗布、乾燥後、又は加熱硬化後に、更に、セラミック
ス形成用原料の液状組成物を一層又は二層以上重ね塗り
し、硬化させて二層以上のゾル−ゲル法によるセラミッ
クス層を形成させることが好ましい。In order to completely prevent the formation of pinholes in the ceramic layer, after the liquid composition of the raw material for forming ceramics is applied, dried, or cured by heating, one or two layers of the liquid composition of the raw material for ceramics is further applied. It is preferable to coat two or more layers and cure them to form two or more ceramic layers by the sol-gel method.
また、セラミックス形成用原料の液状組成物中に、顔料
を添加して用いる場合には、形成されるセラミックス層
上に、更に、顔料を添加していないセラミックス形成用
原料の液状組成物によるセラミックス層を0.5〜40
μm程度の厚さで設けることによって、セラミックス層
の表面層を緻密にして、より撥水性を向上させることが
できる。In addition, when a pigment is added to the liquid composition of the raw material for forming ceramics, a ceramic layer made of the liquid composition of the raw material for ceramics formation to which no pigment is added is added on the ceramic layer to be formed. 0.5~40
By providing the ceramic layer with a thickness of approximately μm, the surface layer of the ceramic layer can be made dense and the water repellency can be further improved.
ゾル−ゲル法によるセラミックス層は、合計厚さ3〜1
50μm程度とすればよい。The ceramic layer formed by the sol-gel method has a total thickness of 3 to 1
The thickness may be approximately 50 μm.
本発明ガスこんろは、各構成部品を組み立てる前に、必
要な金属部品上に上記した方法でセラ・ミックス層を設
け、その後各部品を組み立てる方法、或いは、各部品を
組み立てた後、必要な部品上にセラミックス層を設ける
方法のいずれの方法によっても得られる。また、本発明
ガスこんろでは、すべての金属部品上にセラミックス層
を設ける必要はなく、要求される特性に応じて、必要な
金属部品上にのみセラミックス層を設ければよい。The gas stove of the present invention can be manufactured by providing a ceramic layer on the necessary metal parts by the method described above before assembling each component, and then assembling each part, or by assembling each part and then applying the necessary It can be obtained by any method of providing a ceramic layer on a component. Furthermore, in the gas stove of the present invention, it is not necessary to provide ceramic layers on all metal parts, and it is sufficient to provide ceramic layers only on necessary metal parts depending on the required characteristics.
本発明は、従来の各種のガスこんろに適用でき、例えば
、いわゆるガステープルこんろの他、ガスレンジ、ガス
キャビネット、ガスドロップインこんろ等におけるガス
こんろ部分について適用することができる。The present invention can be applied to various conventional gas stoves, for example, in addition to so-called gas staple stoves, it can be applied to gas stove portions in gas ranges, gas cabinets, gas drop-in stoves, and the like.
発明の効果
本発明によるガスこんろ用金属部品は、ゾル−ゲル法に
よる緻密なセラミックス層を有するものであり、該セラ
ミックス層は、極めて密着性の良好な平滑でピンホール
のない皮膜である。このようなセラミックス層を有する
金属部品は、耐熱性に優れ、高温での金属の酸化を防止
でき、変色や光沢の低下が非常に少ないものである。更
に、表面硬度が高いために傷付き難く、また非汚染性で
あるために食品等による汚れを除去し易く、長期間美感
を維持できるなどの優れた特性を有するものである。ま
た、セラミックス形成用原料の液状組成物中に配合する
顔料を適宜選定することによって自由に着色できるので
、多様な色彩の商品を提供できるという利点もある。Effects of the Invention The metal parts for gas stoves according to the present invention have a dense ceramic layer formed by the sol-gel method, and the ceramic layer is a smooth film with extremely good adhesion and no pinholes. Metal parts having such ceramic layers have excellent heat resistance, can prevent metal oxidation at high temperatures, and have very little discoloration or loss of gloss. Furthermore, it has excellent properties such as being hard to be scratched due to its high surface hardness, and being non-staining, making it easy to remove food stains and maintaining its aesthetic appearance for a long period of time. Furthermore, since it is possible to freely color the liquid composition of the raw material for forming ceramics by appropriately selecting the pigment to be added to the liquid composition, there is also the advantage that products with a variety of colors can be provided.
実施例 以下、実施例を示して本発明を更に詳細に説明する。Example Hereinafter, the present invention will be explained in more detail by showing examples.
実施例1
ガスこんろの構成金属部品である外装カバーガスバーナ
ー、バーナーヘッド、受は皿、及びごとくの各々につい
て、次の方法によりセラミックス層を形成した。Example 1 Ceramic layers were formed on each of the metal components of a gas stove, such as the gas burner cover, the burner head, and the tray, by the following method.
即ち、イソプロピルアルコール15g1微粉末アルミナ
13g1水15g、及びメチルトリメトキシシラン30
gを混合し、これに酸化チタン25g1シリ力15g1
チタン酸カリウム繊維9g及び塩酸0.1gを添加混合
してセラミックス層形成用液状組成物を調製し、これを
スプレー法により前記各部品に塗布し、150℃で20
分間加熱した。That is, 15 g of isopropyl alcohol, 13 g of finely powdered alumina, 15 g of water, and 30 g of methyltrimethoxysilane.
25 g of titanium oxide 1 15 g of silicone
A liquid composition for forming a ceramic layer was prepared by adding and mixing 9 g of potassium titanate fibers and 0.1 g of hydrochloric acid, and this was applied to each of the above parts by a spray method and heated at 150°C for 20 minutes.
Heated for a minute.
この上に上記液状組成物を再度塗布し、150℃で20
分間加熱して合計30μmのゾル−ゲル法による白色の
セラミックス層を形成させた。次いで、酸性コロイド状
シリカ水溶液(濃度30重量%)35g、イソプロピル
アルコール40g及びメチルトリメトキシシラン25g
を混合してセラミックス層形成用液状組成物を調製し、
上記白色セラミックス層上にスプレー法で塗布し、15
0℃で20分間加熱して、厚さ5μmの透明セラミック
ス層を設けた。On top of this, the above liquid composition was applied again and heated to 150°C for 20 minutes.
The mixture was heated for a minute to form a white ceramic layer of 30 μm in total by the sol-gel method. Next, 35 g of acidic colloidal silica aqueous solution (concentration 30% by weight), 40 g of isopropyl alcohol, and 25 g of methyltrimethoxysilane.
to prepare a liquid composition for forming a ceramic layer,
Coated on the above white ceramic layer by spraying method,
A transparent ceramic layer having a thickness of 5 μm was provided by heating at 0° C. for 20 minutes.
得られた各部品について下記の方法により、性能試験を
行なった。結果を第1表に示す。Performance tests were conducted on each of the obtained parts using the following method. The results are shown in Table 1.
1 密 着 性: J I 5K−5400塗膜の密着
性試験
2 硬 度:エンピッ硬度
3 耐傷付き性:ナイロンブラシによる傷付き試験ブラ
ッシング10000回
4 耐 熱 性:400℃または600℃5 耐食塩水
性=2%食塩水滴下、400℃加熱10サイクル
6 塩水噴霧性: J I 5Z2371塩水噴霧試験
1000時間
7 耐沸騰水性:沸騰水浸漬160時間8 耐熱衝撃性
=20℃−600℃1時間づつ100サイクル
9 耐衝撃性:デュポン衝撃試験
10 耐湿潤性: J I 5K−2246湿潤試験
コ、000時間
11 耐汚染性■:食用油250℃加熱後の染み〃
■:食酢による染み
〃 ■:ケチャップ250℃加熱後の
染み
〃 ■:しょう油250℃加熱後の染み〃 ■:バター
250℃加熱後の染み
〃 ■:ソース250℃加熱後の染み
実施例2
Si (OC2H5) 4とZ r (OCA H9)
Aの部分縮合物(C4Hg O) 3 Z r−0−
3L(OC2H5)335gにイソプロピルアルコール
12g1ブチルセルソルブ3g1硅酸ジルコニウム20
g1酸化チタン12g1コバルトクリーン8g、酢酸0
.5gを添加し、混合してセラミックス層形成用液状組
成物を調製し、これをテーブルガスコンロの鋳鉄製ガス
バーナー及び真鍮製ガスバーナーヘッドにスプレー法に
より塗布し、150℃で20分間加熱し、厚さ15μm
のライトグリーンのセラミックス層を設けた。1 Adhesion: JI 5K-5400 Paint film adhesion test 2 Hardness: Empi hardness 3 Scratch resistance: Scratch test with a nylon brush 10,000 brushing times 4 Heat resistance: 400℃ or 600℃ 5 Salt water resistance = Dropwise addition of 2% saline solution, 10 cycles of heating at 400°C 6 Salt water spray properties: J I 5Z2371 salt water spray test 1000 hours 7 Boiling water resistance: Boiling water immersion 160 hours 8 Thermal shock resistance = 100 cycles of 1 hour each from 20°C to 600°C 9 Impact resistance: DuPont impact test 10 Moisture resistance: J I 5K-2246 wet test, 000 hours 11 Stain resistance ■: Stain after heating cooking oil at 250°C
■: Stain caused by vinegar ■: Stain after heating ketchup at 250°C ■: Stain after heating soy sauce at 250°C ■: Stain after heating butter at 250°C ■: Stain after heating sauce at 250°C Example 2 Si ( OC2H5) 4 and Z r (OCA H9)
Partial condensate of A (C4Hg O) 3 Z r-0-
3L (OC2H5) 335g, isopropyl alcohol 12g1 butylcellosolve 3g1, zirconium silicate 20
g1 titanium oxide 12g1 cobalt clean 8g, acetic acid 0
.. 5 g was added and mixed to prepare a liquid composition for forming a ceramic layer, and this was applied to the cast iron gas burner and brass gas burner head of a table gas stove by a spray method, heated at 150°C for 20 minutes, and thickened. 15μm
A light green ceramic layer was provided.
また、イソプロピルアルコール10g、酢酸エチル5g
、及び水15gからなる混合溶媒に粒径20mμの微粉
末アルミナ13g1メチルトリメトキシシラン30g1
チタン白20g1硅酸ジルコニウム15g1コバルトグ
リーン7g、アルミナ繊維9g、及び塩酸0.Igを添
加混合して、セラミックス層形成用液状組成物を調製し
、これを外装カバー、受は皿、ごとくの表面に静電スプ
レー法によって塗布し、150℃で20分間加熱した後
、再度該組成物を塗布し、150℃で20分間加熱して
合計30μmのゾル−ゲル法によるライトグリーンのセ
ラミックス層を形成させた。Also, 10g of isopropyl alcohol, 5g of ethyl acetate
, and 13 g of fine powder alumina with a particle size of 20 mμ 1 30 g of methyltrimethoxysilane in a mixed solvent consisting of 15 g of water
20 g of titanium white, 15 g of zirconium silicate, 7 g of cobalt green, 9 g of alumina fiber, and 0.0 g of hydrochloric acid. A liquid composition for forming a ceramic layer is prepared by adding and mixing Ig, and this is applied to the surface of an exterior cover, a tray, etc. by electrostatic spraying, heated at 150°C for 20 minutes, and then applied again. The composition was applied and heated at 150° C. for 20 minutes to form a light green ceramic layer of 30 μm in total by the sol-gel method.
次いでコロイド状シリカのメタノールゾル溶液(濃度4
0重量%)30sr、イソプロピルアルコール43g1
水2g及びメチルトリメトキシシラン25gを60℃で
加熱混合して得た組成物を上記各部品のセラミックスコ
ーティング層上に静電スプレー法により塗布し、200
℃で20分間加熱して、7μmの透明セラミックス膜を
形成した。Then, a methanol sol solution of colloidal silica (concentration 4
0% by weight) 30sr, isopropyl alcohol 43g1
A composition obtained by heating and mixing 2 g of water and 25 g of methyltrimethoxysilane at 60°C was applied onto the ceramic coating layer of each of the above parts by electrostatic spraying, and
It was heated at ℃ for 20 minutes to form a 7 μm transparent ceramic film.
得られたガスバーナー及びガスバーナーヘッドについて
、実施例1と同様にして性能試験を行なったところ、実
施例1と同様の優れた性能を有するものであった。Performance tests were conducted on the obtained gas burner and gas burner head in the same manner as in Example 1, and they were found to have the same excellent performance as in Example 1.
また、上記した各部品を用いたガスコンロについて、連
続使用6ケ月テストを行なったところ塗膜に変色及び異
常の発生はなかった。また15分間0N10FF 4
000回サイクすテトスを行なった場合にも塗膜に変色
や異常は発生しなかった。Further, when a gas stove using the above-mentioned parts was tested for 6 months of continuous use, no discoloration or abnormality occurred in the coating film. Another 15 minutes 0N10FF 4
No discoloration or abnormality occurred in the coating film even after cycling Tetos 000 times.
以上の結果から判るように、本発明のガスこんろは、熱
による変色や塗膜の剥離が生じることはなく、長期間美
感を維持し得るものであった。As can be seen from the above results, the gas stove of the present invention did not cause discoloration or peeling of the coating due to heat, and was able to maintain its aesthetic appearance for a long period of time.
(以 上)(that's all)
Claims (3)
有するガスこんろ用金属部品。(1) A metal part for a gas stove having a ceramic layer formed by a sol-gel method.
ス形成用原料の液状組成物を塗布し、重合ゲル化させて
セラミックス層を形成することを特徴とするガスこんろ
用金属部品の製造法。(2) A method for manufacturing metal parts for a gas stove, which comprises applying a liquid composition of a raw material for forming ceramics onto the metal parts constituting the gas stove, and polymerizing and gelling the composition to form a ceramic layer. .
有する金属部品を構成部品として有するガスこんろ。(3) A gas stove whose components include metal parts having a ceramic layer formed by a sol-gel method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1073620A JP2602714B2 (en) | 1989-03-24 | 1989-03-24 | Metal parts for gas stove, method for producing metal parts for gas stove, and gas stove |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1073620A JP2602714B2 (en) | 1989-03-24 | 1989-03-24 | Metal parts for gas stove, method for producing metal parts for gas stove, and gas stove |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02251430A true JPH02251430A (en) | 1990-10-09 |
JP2602714B2 JP2602714B2 (en) | 1997-04-23 |
Family
ID=13523553
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1073620A Expired - Lifetime JP2602714B2 (en) | 1989-03-24 | 1989-03-24 | Metal parts for gas stove, method for producing metal parts for gas stove, and gas stove |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2602714B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE9419701U1 (en) * | 1994-12-08 | 1996-04-11 | M. Faist GmbH & Co KG, 86381 Krumbach | Thermal protection component |
WO2003012341A1 (en) * | 2001-08-02 | 2003-02-13 | Thermic Investments S.A. | Atmospheric gas burner made of biosoluble and gel-cast ceramic fibers |
JP2014099420A (en) * | 2014-03-03 | 2014-05-29 | Mitsubishi Electric Corp | Heating cooker |
JP2014148704A (en) * | 2013-01-31 | 2014-08-21 | Osaka Gas Chem Kk | Composition for outermost surface of gas cooking appliance |
JP2016093535A (en) * | 2016-01-12 | 2016-05-26 | 東芝ホームテクノ株式会社 | Cooker |
JP2020153538A (en) * | 2019-03-18 | 2020-09-24 | 株式会社ノーリツ | Burner cap, stove burner and heating cooker |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5348346U (en) * | 1976-09-29 | 1978-04-24 | ||
US4472510A (en) * | 1982-12-23 | 1984-09-18 | Dow Corning Corporation | Carbon-containing monolithic glasses and ceramics prepared by a sol-gel process |
JPS6232157A (en) * | 1985-08-02 | 1987-02-12 | Yoshio Ichikawa | Coating composition |
JPS6375073A (en) * | 1986-09-17 | 1988-04-05 | Yoshio Ichikawa | Coating method |
JPS63143778A (en) * | 1986-12-05 | 1988-06-16 | 松下電器産業株式会社 | Manufacture of electric heating unit |
JPS63306035A (en) * | 1987-06-08 | 1988-12-14 | Nisshin Steel Co Ltd | Infrared radiating plate and manufacture thereof |
-
1989
- 1989-03-24 JP JP1073620A patent/JP2602714B2/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5348346U (en) * | 1976-09-29 | 1978-04-24 | ||
US4472510A (en) * | 1982-12-23 | 1984-09-18 | Dow Corning Corporation | Carbon-containing monolithic glasses and ceramics prepared by a sol-gel process |
JPS6232157A (en) * | 1985-08-02 | 1987-02-12 | Yoshio Ichikawa | Coating composition |
JPS6375073A (en) * | 1986-09-17 | 1988-04-05 | Yoshio Ichikawa | Coating method |
JPS63143778A (en) * | 1986-12-05 | 1988-06-16 | 松下電器産業株式会社 | Manufacture of electric heating unit |
JPS63306035A (en) * | 1987-06-08 | 1988-12-14 | Nisshin Steel Co Ltd | Infrared radiating plate and manufacture thereof |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE9419701U1 (en) * | 1994-12-08 | 1996-04-11 | M. Faist GmbH & Co KG, 86381 Krumbach | Thermal protection component |
WO2003012341A1 (en) * | 2001-08-02 | 2003-02-13 | Thermic Investments S.A. | Atmospheric gas burner made of biosoluble and gel-cast ceramic fibers |
US7537447B2 (en) | 2001-08-02 | 2009-05-26 | Thermic Investments S.A. | Atmospheric gas burner made of biosoluble and gel-cast ceramic fibers |
JP2014148704A (en) * | 2013-01-31 | 2014-08-21 | Osaka Gas Chem Kk | Composition for outermost surface of gas cooking appliance |
JP2014099420A (en) * | 2014-03-03 | 2014-05-29 | Mitsubishi Electric Corp | Heating cooker |
JP2016093535A (en) * | 2016-01-12 | 2016-05-26 | 東芝ホームテクノ株式会社 | Cooker |
JP2020153538A (en) * | 2019-03-18 | 2020-09-24 | 株式会社ノーリツ | Burner cap, stove burner and heating cooker |
Also Published As
Publication number | Publication date |
---|---|
JP2602714B2 (en) | 1997-04-23 |
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