CN109321133A - Coating composition and preparation method thereof, coating piece and preparation method thereof, household electrical appliance - Google Patents
Coating composition and preparation method thereof, coating piece and preparation method thereof, household electrical appliance Download PDFInfo
- Publication number
- CN109321133A CN109321133A CN201811175205.8A CN201811175205A CN109321133A CN 109321133 A CN109321133 A CN 109321133A CN 201811175205 A CN201811175205 A CN 201811175205A CN 109321133 A CN109321133 A CN 109321133A
- Authority
- CN
- China
- Prior art keywords
- polysilazane
- coating composition
- perfluor
- raw material
- range
- 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
- 239000008199 coating composition Substances 0.000 title claims abstract description 165
- 239000011248 coating agent Substances 0.000 title claims abstract description 118
- 238000000576 coating method Methods 0.000 title claims abstract description 118
- 238000002360 preparation method Methods 0.000 title claims abstract description 64
- 239000002994 raw material Substances 0.000 claims abstract description 255
- 229920001709 polysilazane Polymers 0.000 claims abstract description 199
- -1 polysiloxanes Polymers 0.000 claims abstract description 193
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 190
- 239000003086 colorant Substances 0.000 claims abstract description 68
- 239000011737 fluorine Substances 0.000 claims abstract description 58
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 58
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 57
- 239000002519 antifouling agent Substances 0.000 claims abstract description 52
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 75
- 239000002904 solvent Substances 0.000 claims description 69
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 62
- 239000003054 catalyst Substances 0.000 claims description 62
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 60
- 239000001257 hydrogen Substances 0.000 claims description 60
- 229910052739 hydrogen Inorganic materials 0.000 claims description 60
- 239000000945 filler Substances 0.000 claims description 59
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims description 52
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 32
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 30
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 30
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims description 30
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 claims description 30
- 239000006229 carbon black Substances 0.000 claims description 29
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 29
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 29
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 25
- 239000011159 matrix material Substances 0.000 claims description 25
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims description 24
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 23
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims description 22
- 150000001412 amines Chemical group 0.000 claims description 22
- 239000011787 zinc oxide Substances 0.000 claims description 21
- 235000014692 zinc oxide Nutrition 0.000 claims description 21
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 20
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 20
- 125000003118 aryl group Chemical group 0.000 claims description 19
- 239000004005 microsphere Substances 0.000 claims description 19
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 19
- 150000001924 cycloalkanes Chemical class 0.000 claims description 18
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims description 17
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 17
- 239000010941 cobalt Substances 0.000 claims description 16
- 229910017052 cobalt Inorganic materials 0.000 claims description 16
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 16
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 16
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 claims description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 15
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 15
- 235000010215 titanium dioxide Nutrition 0.000 claims description 15
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 14
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 13
- 239000002585 base Substances 0.000 claims description 13
- 239000010936 titanium Substances 0.000 claims description 13
- 229910052719 titanium Inorganic materials 0.000 claims description 13
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 12
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 12
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 claims description 11
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 claims description 10
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 10
- 239000000919 ceramic Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 10
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 10
- 239000011521 glass Substances 0.000 claims description 10
- 150000002576 ketones Chemical class 0.000 claims description 10
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 claims description 10
- 239000000395 magnesium oxide Substances 0.000 claims description 10
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 9
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims description 9
- 239000000440 bentonite Substances 0.000 claims description 9
- 229910000278 bentonite Inorganic materials 0.000 claims description 9
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 9
- 239000000835 fiber Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- 229960004692 perflenapent Drugs 0.000 claims description 9
- 229960004624 perflexane Drugs 0.000 claims description 9
- 241000907663 Siproeta stelenes Species 0.000 claims description 8
- 150000002940 palladium Chemical class 0.000 claims description 8
- 241000894007 species Species 0.000 claims description 8
- 239000005995 Aluminium silicate Substances 0.000 claims description 7
- 235000012211 aluminium silicate Nutrition 0.000 claims description 7
- 150000008331 benzenesulfonamides Chemical class 0.000 claims description 7
- 239000000038 blue colorant Substances 0.000 claims description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 7
- LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 claims description 7
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 claims description 7
- 239000000049 pigment Substances 0.000 claims description 7
- 239000001062 red colorant Substances 0.000 claims description 7
- 239000012463 white pigment Substances 0.000 claims description 7
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 6
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 claims description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 6
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 6
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 6
- OBNDGIHQAIXEAO-UHFFFAOYSA-N [O].[Si] Chemical compound [O].[Si] OBNDGIHQAIXEAO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052787 antimony Inorganic materials 0.000 claims description 6
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 6
- 150000004982 aromatic amines Chemical class 0.000 claims description 6
- 229910000152 cobalt phosphate Inorganic materials 0.000 claims description 6
- ZBDSFTZNNQNSQM-UHFFFAOYSA-H cobalt(2+);diphosphate Chemical group [Co+2].[Co+2].[Co+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O ZBDSFTZNNQNSQM-UHFFFAOYSA-H 0.000 claims description 6
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 6
- DGXKDBWJDQHNCI-UHFFFAOYSA-N dioxido(oxo)titanium nickel(2+) Chemical group [Ni++].[O-][Ti]([O-])=O DGXKDBWJDQHNCI-UHFFFAOYSA-N 0.000 claims description 6
- PCHPORCSPXIHLZ-UHFFFAOYSA-N diphenhydramine hydrochloride Chemical compound [Cl-].C=1C=CC=CC=1C(OCC[NH+](C)C)C1=CC=CC=C1 PCHPORCSPXIHLZ-UHFFFAOYSA-N 0.000 claims description 6
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 6
- 239000001056 green pigment Substances 0.000 claims description 6
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 claims description 6
- 239000001053 orange pigment Substances 0.000 claims description 6
- 238000010422 painting Methods 0.000 claims description 6
- 229910052763 palladium Inorganic materials 0.000 claims description 6
- YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical compound CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 claims description 6
- ZJIJAJXFLBMLCK-UHFFFAOYSA-N perfluorohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZJIJAJXFLBMLCK-UHFFFAOYSA-N 0.000 claims description 6
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 claims description 6
- 229960001124 trientine Drugs 0.000 claims description 6
- 239000001060 yellow colorant Substances 0.000 claims description 6
- XRKOOHTZZDPJNE-UHFFFAOYSA-N 1,1,1-trifluorohexane Chemical compound CCCCCC(F)(F)F XRKOOHTZZDPJNE-UHFFFAOYSA-N 0.000 claims description 5
- KGYUZRBIQCDOCN-UHFFFAOYSA-N 2-(2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptyl)oxirane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CC1CO1 KGYUZRBIQCDOCN-UHFFFAOYSA-N 0.000 claims description 5
- AEFDMRZYGPZNIT-UHFFFAOYSA-N CCC(C(CCF)C(F)(F)F)C(F)(F)F Chemical compound CCC(C(CCF)C(F)(F)F)C(F)(F)F AEFDMRZYGPZNIT-UHFFFAOYSA-N 0.000 claims description 5
- UMUXBDSQTCDPJZ-UHFFFAOYSA-N chromium titanium Chemical compound [Ti].[Cr] UMUXBDSQTCDPJZ-UHFFFAOYSA-N 0.000 claims description 5
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 claims description 5
- 229940043276 diisopropanolamine Drugs 0.000 claims description 5
- 229910052631 glauconite Inorganic materials 0.000 claims description 5
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical class CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 claims description 5
- MECMQNITHCOSAF-UHFFFAOYSA-N manganese titanium Chemical group [Ti].[Mn] MECMQNITHCOSAF-UHFFFAOYSA-N 0.000 claims description 5
- KAVGMUDTWQVPDF-UHFFFAOYSA-N perflubutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)F KAVGMUDTWQVPDF-UHFFFAOYSA-N 0.000 claims description 5
- 239000003208 petroleum Substances 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 claims description 4
- GXTNDOSGOPRCEO-UHFFFAOYSA-N [Cr].[Fe].[Zn] Chemical compound [Cr].[Fe].[Zn] GXTNDOSGOPRCEO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- GZCWPZJOEIAXRU-UHFFFAOYSA-N tin zinc Chemical group [Zn].[Sn] GZCWPZJOEIAXRU-UHFFFAOYSA-N 0.000 claims description 4
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 3
- QHWFBGRTHMNLGS-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-henicosafluorooctadecane Chemical compound CCCCCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F QHWFBGRTHMNLGS-UHFFFAOYSA-N 0.000 claims description 3
- UVWPNDVAQBNQBG-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-icosafluorononane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F UVWPNDVAQBNQBG-UHFFFAOYSA-N 0.000 claims description 3
- SSVQUYHNTDJHGP-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorooctadecane Chemical compound CCCCCCCCCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SSVQUYHNTDJHGP-UHFFFAOYSA-N 0.000 claims description 3
- SKRWRXWNQFQGRU-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorooctane Chemical compound CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SKRWRXWNQFQGRU-UHFFFAOYSA-N 0.000 claims description 3
- OKIYQFLILPKULA-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluoro-4-methoxybutane Chemical class COC(F)(F)C(F)(F)C(F)(F)C(F)(F)F OKIYQFLILPKULA-UHFFFAOYSA-N 0.000 claims description 3
- CDMCLELUDINUDU-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexylbenzene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C1=CC=CC=C1 CDMCLELUDINUDU-UHFFFAOYSA-N 0.000 claims description 3
- GHBZJUJZNRLHBI-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,6-decafluoro-5,6-bis(trifluoromethyl)cyclohexane Chemical compound FC(F)(F)C1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C1(F)C(F)(F)F GHBZJUJZNRLHBI-UHFFFAOYSA-N 0.000 claims description 3
- PEGQMHNLNMIEQD-UHFFFAOYSA-N 1,1-difluorohexane Chemical compound CCCCCC(F)F PEGQMHNLNMIEQD-UHFFFAOYSA-N 0.000 claims description 3
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims description 3
- ZWXJTBZOZHXIAY-UHFFFAOYSA-N 1,7-difluoroheptane Chemical compound FCCCCCCCF ZWXJTBZOZHXIAY-UHFFFAOYSA-N 0.000 claims description 3
- DFUYAWQUODQGFF-UHFFFAOYSA-N 1-ethoxy-1,1,2,2,3,3,4,4,4-nonafluorobutane Chemical compound CCOC(F)(F)C(F)(F)C(F)(F)C(F)(F)F DFUYAWQUODQGFF-UHFFFAOYSA-N 0.000 claims description 3
- NHCREQREVZBOCH-UHFFFAOYSA-N 1-methyl-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalene Chemical class C1CCCC2C(C)CCCC21 NHCREQREVZBOCH-UHFFFAOYSA-N 0.000 claims description 3
- JDKBATJPUKFKDT-UHFFFAOYSA-N CCCCCC.[F] Chemical class CCCCCC.[F] JDKBATJPUKFKDT-UHFFFAOYSA-N 0.000 claims description 3
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 3
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 3
- ODNDNQIUXLSMAB-UHFFFAOYSA-N [Mn].[Y].[In] Chemical compound [Mn].[Y].[In] ODNDNQIUXLSMAB-UHFFFAOYSA-N 0.000 claims description 3
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 3
- 229930016911 cinnamic acid Natural products 0.000 claims description 3
- 235000013985 cinnamic acid Nutrition 0.000 claims description 3
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims description 3
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 claims description 3
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 3
- 239000002480 mineral oil Substances 0.000 claims description 3
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 claims description 3
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 3
- NJCBUSHGCBERSK-UHFFFAOYSA-N perfluoropentane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F NJCBUSHGCBERSK-UHFFFAOYSA-N 0.000 claims description 3
- 239000010702 perfluoropolyether Substances 0.000 claims description 3
- 150000003053 piperidines Chemical class 0.000 claims description 3
- BXRQHCUOIXCKHD-UHFFFAOYSA-M potassium 6,6,6-trifluorohexane-1-sulfonate Chemical compound FC(CCCCCS(=O)(=O)[O-])(F)F.[K+] BXRQHCUOIXCKHD-UHFFFAOYSA-M 0.000 claims description 3
- 235000019260 propionic acid Nutrition 0.000 claims description 3
- UBXAKNTVXQMEAG-UHFFFAOYSA-L strontium sulfate Inorganic materials [Sr+2].[O-]S([O-])(=O)=O UBXAKNTVXQMEAG-UHFFFAOYSA-L 0.000 claims description 3
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- AXFFGMPNSZVEDX-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,17,17,18,18,19,19,20,20,21,21,22,22,23,23,24,24,24-pentacontafluorotetracosane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F AXFFGMPNSZVEDX-UHFFFAOYSA-N 0.000 claims description 2
- FEBCMJRMESQQMH-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexadecane Chemical compound CCCCCCCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F FEBCMJRMESQQMH-UHFFFAOYSA-N 0.000 claims description 2
- LOJJTTDNNWYSGX-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluoro-4-(1,1,2,2,3,3,4,4,4-nonafluorobutoxy)butane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)OC(F)(F)C(F)(F)C(F)(F)C(F)(F)F LOJJTTDNNWYSGX-UHFFFAOYSA-N 0.000 claims description 2
- ZVXOHSHODRJTCP-UHFFFAOYSA-N 1,1,2,2,3,3,4-heptafluoro-4-(trifluoromethyl)cyclobutane Chemical compound FC(F)(F)C1(F)C(F)(F)C(F)(F)C1(F)F ZVXOHSHODRJTCP-UHFFFAOYSA-N 0.000 claims description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical group ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 2
- QFLWRXCREKXVBP-UHFFFAOYSA-N 1-methyl-3-(trifluoromethyl)pyrrolidin-2-one Chemical compound FC(C1C(N(CC1)C)=O)(F)F QFLWRXCREKXVBP-UHFFFAOYSA-N 0.000 claims description 2
- CGWDABYOHPEOAD-UHFFFAOYSA-N 2-[(4-fluorophenoxy)methyl]oxirane Chemical compound C1=CC(F)=CC=C1OCC1OC1 CGWDABYOHPEOAD-UHFFFAOYSA-N 0.000 claims description 2
- NSHDLZDDSBGOKN-UHFFFAOYSA-N 2-[2,2,3,3,4,4,5,5,6,7,7,7-dodecafluoro-6-(trifluoromethyl)heptyl]oxirane Chemical compound FC(F)(F)C(F)(C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CC1CO1 NSHDLZDDSBGOKN-UHFFFAOYSA-N 0.000 claims description 2
- AUNULSXNIRWLBZ-UHFFFAOYSA-N 5,5-dimethyl-2-(1,1,2,2,2-pentafluoroethyl)cyclohexa-1,3-diene Chemical compound CC1(C)CC=C(C=C1)C(C(F)(F)F)(F)F AUNULSXNIRWLBZ-UHFFFAOYSA-N 0.000 claims description 2
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 claims description 2
- 239000001282 iso-butane Substances 0.000 claims description 2
- 235000013847 iso-butane Nutrition 0.000 claims description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims description 2
- BPHQIXJDBIHMLT-UHFFFAOYSA-N perfluorodecane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F BPHQIXJDBIHMLT-UHFFFAOYSA-N 0.000 claims description 2
- ODOPKAJVFRHHGM-UHFFFAOYSA-N phenyltin Chemical compound [Sn]C1=CC=CC=C1 ODOPKAJVFRHHGM-UHFFFAOYSA-N 0.000 claims description 2
- OCEBOBGSOQRMQZ-UHFFFAOYSA-N trifluoromethylcyclopentane Chemical compound FC(F)(F)C1CCCC1 OCEBOBGSOQRMQZ-UHFFFAOYSA-N 0.000 claims description 2
- 238000006555 catalytic reaction Methods 0.000 claims 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims 1
- OEPRBXUJOQLYID-UHFFFAOYSA-N 1-fluoropentane Chemical compound CCCCCF OEPRBXUJOQLYID-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 241001062009 Indigofera Species 0.000 claims 1
- 241000382362 Persicaria tinctoria Species 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- 229910003978 SiClx Inorganic materials 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- SHLNMHIRQGRGOL-UHFFFAOYSA-N barium zinc Chemical compound [Zn].[Ba] SHLNMHIRQGRGOL-UHFFFAOYSA-N 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- HEQBUZNAOJCRSL-UHFFFAOYSA-N iron(ii) chromite Chemical compound [O-2].[O-2].[O-2].[Cr+3].[Fe+3] HEQBUZNAOJCRSL-UHFFFAOYSA-N 0.000 claims 1
- UHHKSVZZTYJVEG-UHFFFAOYSA-N oxepane Chemical compound C1CCCOCC1 UHHKSVZZTYJVEG-UHFFFAOYSA-N 0.000 claims 1
- 125000005005 perfluorohexyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- MTZWHHIREPJPTG-UHFFFAOYSA-N phorone Chemical compound CC(C)=CC(=O)C=C(C)C MTZWHHIREPJPTG-UHFFFAOYSA-N 0.000 claims 1
- 229930193351 phorone Natural products 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 235000013305 food Nutrition 0.000 abstract description 13
- 230000003670 easy-to-clean Effects 0.000 abstract description 10
- 238000003756 stirring Methods 0.000 description 24
- 238000000034 method Methods 0.000 description 21
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 10
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 8
- 239000000758 substrate Substances 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 241000209094 Oryza Species 0.000 description 4
- 235000007164 Oryza sativa Nutrition 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 4
- 235000009566 rice Nutrition 0.000 description 4
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 4
- AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-Me3C6H3 Natural products CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000002203 pretreatment Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 231100000611 venom Toxicity 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IWIJPSWAAIRVQF-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluorodocosane Chemical compound CCCCCCCCCCCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F IWIJPSWAAIRVQF-UHFFFAOYSA-N 0.000 description 2
- VDMQXMQJUHCJLX-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-icosafluorodecane Chemical compound FC(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)F VDMQXMQJUHCJLX-UHFFFAOYSA-N 0.000 description 2
- HWGNOHFZECDUBX-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,7,7,7-undecafluoroheptan-2-one Chemical compound CC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F HWGNOHFZECDUBX-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 2
- 244000246386 Mentha pulegium Species 0.000 description 2
- 235000016257 Mentha pulegium Nutrition 0.000 description 2
- 235000004357 Mentha x piperita Nutrition 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000005376 alkyl siloxane group Chemical group 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000003373 anti-fouling effect Effects 0.000 description 2
- GHPGOEFPKIHBNM-UHFFFAOYSA-N antimony(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Sb+3].[Sb+3] GHPGOEFPKIHBNM-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 235000001050 hortel pimenta Nutrition 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- CSHCPECZJIEGJF-UHFFFAOYSA-N methyltin Chemical compound [Sn]C CSHCPECZJIEGJF-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 230000007096 poisonous effect Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052596 spinel Inorganic materials 0.000 description 2
- 239000011029 spinel Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- OFZYBEBWCZBCPM-UHFFFAOYSA-N 1,1-dimethylcyclobutane Chemical compound CC1(C)CCC1 OFZYBEBWCZBCPM-UHFFFAOYSA-N 0.000 description 1
- RFXPCNNPYDLUIC-UHFFFAOYSA-N 1-fluoro-1,2-dimethylcyclohexane Chemical group CC1CCCCC1(C)F RFXPCNNPYDLUIC-UHFFFAOYSA-N 0.000 description 1
- WZFYIEQSKFOFKB-UHFFFAOYSA-N 1-fluoro-2,7-dimethyloctane Chemical compound FCC(CCCCC(C)C)C WZFYIEQSKFOFKB-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 108091005950 Azurite Proteins 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- 239000004965 Silica aerogel Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- UMVBXBACMIOFDO-UHFFFAOYSA-N [N].[Si] Chemical compound [N].[Si] UMVBXBACMIOFDO-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- OOBNORVQFIAGPT-UHFFFAOYSA-N antimony manganese Chemical compound [Mn].[Sb] OOBNORVQFIAGPT-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- FANANXQSVYPRCQ-UHFFFAOYSA-N azane;silicon Chemical compound N.[Si] FANANXQSVYPRCQ-UHFFFAOYSA-N 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
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- 238000003703 image analysis method Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229940098458 powder spray Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- POOSGDOYLQNASK-UHFFFAOYSA-N tetracosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC POOSGDOYLQNASK-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- GWBUNZLLLLDXMD-UHFFFAOYSA-H tricopper;dicarbonate;dihydroxide Chemical compound [OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[O-]C([O-])=O.[O-]C([O-])=O GWBUNZLLLLDXMD-UHFFFAOYSA-H 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/16—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers in which all the silicon atoms are connected by linkages other than oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
The present invention provides the household electrical appliance of a kind of coating composition, the preparation method of the coating composition, the coating piece as obtained by the coating composition, the preparation method and application of the coating piece coating piece.The coating composition prepares the anti-fouling agent and colorant that raw material includes polysilazane, polysiloxanes, fluorine richness, the polysilazane and polysiloxanes are copolymerized generation polysilazane-polysiloxane copolymer, and the anti-fouling agent and colorant of the fluorine richness are mixed with the polysilazane-polysiloxane copolymer.Present invention coating as obtained by the coating composition not only has the advantages that hardness is high, adhesion is good, easy to clean, temperature tolerance is good, reaches food touch-safe rank, also has preferable appearance.
Description
Technical field
The present invention relates to the preparations of field of home appliance technology more particularly to a kind of coating composition, the coating composition
Method, the coating piece as obtained by the coating composition, the preparation method and application of the coating piece coating piece household electrical appliance.
Background technique
In micro- roasting field, it usually needs form coating in the surface of kitchen appliance class product, the material of above-mentioned coating is main are as follows: porcelain
Glaze (enamel can be formed in product surface enamel technology), organosilicon, epoxy powder (can be used the ring by way of dusting
Oxygen powder spray is in product surface) or silica solution+organic-silicon hybridization coating.However, above-mentioned coating also has, hardness is low, adheres to
Property is poor, not easy to clean, temperature tolerance is poor and not up to food touch-safe rank the disadvantages of.Moreover, above-mentioned coating also has appearance
Inaesthetic disadvantage.
Summary of the invention
The main purpose of the present invention is to provide a kind of coating compositions, it is intended to make the painting as obtained by the coating composition
Layer not only has the advantages that hardness is high, adhesion is good, temperature tolerance is good, easy to clean and can reach food touch-safe, also with compared with
Good appearance.
In order to solve the above technical problems, the raw material for preparing of coating composition provided by the invention includes polysilazane, poly- silicon
The anti-fouling agent and colorant of oxygen alkane, fluorine richness, the polysilazane and polysiloxanes are copolymerized generation polysilazane-poly- silicon
Siloxane copolymers, the anti-fouling agent and colorant of the fluorine richness are mixed with the polysilazane-polysiloxane copolymer.
Further, it is 7~50% that the polysilazane, which accounts for the range of the mass percent for preparing raw material, described poly-
The range that siloxanes accounts for the mass percent for preparing raw material is 3~40%, and the anti-fouling agent of the fluorine richness accounts for the preparation
The range of the mass percent of raw material is 0.01~20%, and the range that the colorant accounts for the mass percent for preparing raw material is
0.01~5%.
Further, the colorant is selected from white pigment, yellow colorant, orange pigment, black pigment, purple, palm fibre
At least one of color colorant, green pigment, blue colorant, grey colorant and red colorant.
Further, the white pigment is selected from least one of stibium trioxide, barium sulfate, lithopone, titanium white and zinc white;
And/or
The yellow colorant is nickel titanate antimony and/or titanium chromium palm fibre;And/or
The orange pigment is zinc-tin rutile;And/or
The black pigment is selected from copper-chrome black spinelle, titanium is black, in manganese dioxide, Ma Sihei, ivory black and carbon black extremely
Few one kind;And/or
The purple is cobalt phosphate;And/or
The brown colorant is titanium manganese brown and/or zinc-iron chromium palm fibre;And/or
The green pigment is selected from least one of cobalt green, malachite and glauconite;And/or
The blue colorant is selected from celestine, cobalt blue, Egyptian blue, the Chinese are blue, at least one in chessy copper and yttrium indium manganese basket
Kind;And/or
The grey colorant be black copper-chrome black spinelle, titanium, manganese dioxide, Ma Sihei, violet black, in ivory black and carbon black
At least one mixture or the grey colorant at least one of with stibium trioxide, barium sulfate, lithopone, titanium white and zinc white
For copper-chrome black spinelle, titanium is black, at least one of manganese dioxide, Ma Sihei, violet black, ivory black and carbon black, with stibium trioxide, sulphur
The mixing of at least one of sour barium, lithopone, titanium white and zinc white and at least one of burnt ochre, Indian red and cobalt blue
Object;And/or
The red colorant is selected from least one of burnt sienna, burnt ochre and Indian red.
Further, the anti-fouling agent of the fluorine richness is selected from methyl perfluoro amyl ketone, 1- methyl -3- trifluoromethyl -2- pyrrole
Pyrrolidone, 1H, 1H- perfluor -1- tetradecyl alchohol, 1- fluorine heptane, ten trifluorohexane -1- sulfonic acid potassium salts, perfluor pentane, [(4- fluorobenzene
Oxygroup) methyl] ethylene oxide, 2H- perfluor -5,8,11,14,17- pentamethyls -3,6,9,12,15,18- six oxa- heneicosanes,
Ten difluoro hexane of 2- (trifluoromethyl) -3- ethyoxyl, ten fluoro- 4- (pentafluoroethyl group) oxepane sulfonic acid potassium salts, 1,1,1,2,2,
3,4,5,5,6,6,6- ten two fluoro- 3,4- bis- (trifluoromethyl) hexanes, perfluor eicosane, 1H, 6H- perflexane, 1,7- difluoro
Heptane, 1,1,1,2,2,3,3,4,5,5,6,6,6- ten trifluorohexane, 1,1,2,2,5,5,6,6- pungent fluorine hexane, perfluor are to peppermint
It is alkane, heptafluoro-propane, PF 5070, perfluor (methyl decahydronaphthalenes), perfluoropolyether, perfluor -1- butane sulfonic acid, perflenapent, complete
It is fluorine (hexahydrotoluene), perfluor (2,2,3,3- 4-methyl-butane), perfluor -1- octane, perflexane, N- perfluor n-decane, complete
It is fluoro -1,2- dimethyl cyclohexane, perfluor pentadecane, Perfluorononane, Sonazoid, perfluor dodecane, the perfluor tetradecane, complete
Fluoro- 2,7- dimethyl octane, perfluor hexadecane, perfluor -2,3,5,6- tetramethyl-ring hexanes, perfluor tridecane, perfluoro-methyl ring
Pentane, perfluoro-2-methyl cyclobutane, (perfluoro hexyl) benzene, perfluor-(1,3,5- trimethylbenzene), perfluorobutyl ethane, perfluor fourth
Base ether, perfluorotetracosane, perfluoro hexyl ethane, perfluor tetraethyleneglycol dimethyl ether, perfluor -2- methybutane, perfluor are to peppermint
Alkane, perfluorooctyl ethane, 3- (perfluoro hexyl) propylene oxide, 3- (perfluoro hexyl) propylene oxide, 3- (2- perfluoro hexyl ethoxy
Base) -1,2- propylene oxide, 3- (Sonazoid) -1,2- propylene oxide, 3- (perfluoro-n-octane) -1,2- propylene oxide, 1H,
1H- perfluor -1- the tetradecane, 2H- perfluor 15- methyl -3,6- dioxanonane, 3- (perfluor -5- methylhexyl) -1,2- epoxy third
Alkane, 1H- perflenapent, 1- (perfluor-n- hexyl) dodecane, 1- (perfluor-n- octyl) tetradecane, 1H, 6H- perflexane, 1-
(perfluor-n- hexyl) decane, 1H- perfluor -2,4,4,-trimethylpentane, 1H, 10H- perfluoro decane, 1H- perfluor -2,6- diformazan
Base heptane, 1- methyl -4- (perfluoro-ethyl) toluene, 2H- perfluor (2- methylpentane), ethyl perfluorobutyl ether, 8- perfluoro decyl
Octane, perfluor iso-butane, perfluorobutyl methyl ethers, perfluoro propene oxid, 2- trifluoromethyl perflenapent and 2H-3H- perfluor penta
At least one of alkane.
Further, the structural formula of the polysilazane are as follows:Wherein, R1For hydrogen-based, alkane, cycloalkane,
Olefine, aryl, alkoxy, alkyl siloxy or alkylamino radical, R2For hydrogen-based, alkane, cycloalkane, olefine, aryl, alcoxyl
Base, alkyl siloxy or alkylamino radical, R3For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy, alkyl siloxy or
Alkylamino radical.
Further, the R1And R2At least one of be hydrogen-based or olefine.
Further, the molecular weight of the polysilazane is 100~1000.
Further, the structural formula of the polysiloxanes are as follows:Wherein, R4For hydrogen-based, alkane, cycloalkane,
Olefine, aryl, alkoxy or alkyl siloxy, R5For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy or alkane
Base siloxy.
Further, the molecular weight of the polysiloxanes is 100~1300.
Further, the raw material for preparing of the coating composition further includes solvent, and the solvent accounts for the coating composition
Mass percent range be 10~66%, the solvent be selected from alkane solvents, ether solvent, ketones solvent and benzene spread out
At least one of biological species solvent.
Further, the alkane solvents are selected from n-hexane, normal octane, n-decane, chloroform, methylene chloride, two
At least one of vinyl chloride and mineral oil are a variety of;The ether solvent in ether, petroleum ether and butyl oxide extremely
Few one kind;The ketones solvent is selected from least one of acetone, methyl ethyl ketone, cyclohexanone and isophorone;The benzene derivative
Class solvent is selected from least one of toluene, meta-xylene, paraxylene, ortho-xylene and chlorobenzene.
Further, the raw material for preparing of the coating composition further includes catalyst, and it is former that the catalyst accounts for the preparation
The range of the mass percent of material is 0.01~5%, and the catalyst is amines catalyst and/or metal-based catalysts.
Further, the amines catalyst is selected from one of fatty amine, cycloaliphatic amines, hydramine and aromatic amine or more
Kind, the fatty amine is selected from least one of diethylamine, triethylamine and triethylene tetramine;The cycloaliphatic amines are selected from Sanya
At least one of ethyldiamine, piperazine, piperidines and morpholine;The hydramine is selected from N, N- dimethylethanolamine, diisopropanol
Amine and N, at least one of N- diethyl ethylene diamine;The aromatic amine is selected from aniline, o-phenylenediamine, benzidine and N, N- bis-
At least one of methylaniline.
Further, the metal-based catalysts be organotin catalysts and/or palladium class catalyst, it is described organotin catalyzed
Agent is selected from least one of dibutyltindilaurylmercaptide cinnamic acid rouge, stannous octoate, stannous methide and triphenyltin;The palladium class is urged
Agent is selected from least one of carbon/palladium, palladium chloride, propionic acid palladium salt, acetic acid palladium salt and triphenyl phosphorus palladium.
Further, the raw material for preparing of the coating composition further includes filler, and the filler accounts for the raw material for preparing
The range of mass percent is 1~50%, and the filler is selected from silicon carbide, aluminium oxide, titanium oxide, zinc oxide, magnesia, hydrogen-oxygen
Change at least one of aluminium, white carbon black, concave convex rod, kaolin, bentonite, glass microsphere and ceramic microsphere.
Further, the raw material for preparing of the coating composition further includes catalyst and filler, and the catalyst accounts for described
The range of the mass percent of coating composition is 0.01~5%, and the filler accounts for the mass percent of the coating composition
Range be 1~50%, the range for the mass percent that the polysiloxanes accounts for the coating composition with polysilazane is
10%~60%, the range that the anti-fouling agent of the fluorine richness accounts for the mass percent for preparing raw material is 0.01~15%.
The present invention also provides a kind of preparation methods of coating composition, comprising the following steps:
Offer prepares raw material, described to prepare the anti-fouling agent and colorant that raw material includes polysilazane, polysiloxanes, fluorine richness;
Mixing polysilazane and polysiloxanes, polysilazane and polysiloxanes are copolymerized, and it is poly- to generate polysilazane-
Silicone copolymers;
The anti-fouling agent and colorant of fluorine richness are added into the polysilazane-polysiloxane copolymer, the coating is made
Composition.
Further, after mixing polysilazane and polysiloxanes, the preparation method of the coating composition further include: Xiang Ju
The step of catalyst is added in silazane and polysiloxanes, wherein the catalyst accounts for the mass percent for preparing raw material
Range be 0.01~5%, the catalyst be amines catalyst and/or metal-based catalysts.
Further, after generating polysilazane-polysiloxane copolymer, before obtaining the coating composition, the coating
The preparation method of composition further include: the step of solvent is added into polysilazane-polysiloxane copolymer, wherein described molten
Agent account for the mass percent for preparing raw material range be 10~66%, the solvent be selected from alkane solvents, ether solvent,
At least one of ketones solvent and benzenesulfonamide derivative species solvent.
Further, after generating polysilazane-polysiloxane copolymer, before obtaining the coating composition, the coating
The preparation method of composition further include: the step of filler is added into polysilazane-polysiloxane copolymer, wherein described to fill out
Material account for the mass percent for preparing raw material range be 1~50%, the filler be selected from silicon carbide, aluminium oxide, titanium oxide,
In zinc oxide, magnesia, aluminium hydroxide, white carbon black, concave convex rod, kaolin, bentonite, glass microsphere and ceramic microsphere extremely
Few one kind.
The present invention also provides a kind of coating piece, the coating piece includes matrix and the coating for being formed in matrix surface, described
Contain the coating composition in coating.
Further, the range of the thickness of the coating is 1~100 micron.
The present invention also provides a kind of preparation methods of coating piece, comprising the following steps:
Matrix and the coating composition are provided;
By the coating composition in the surface of matrix, the coating piece is made.
The present invention also provides a kind of household electrical appliance, the household electrical appliance include the coating piece.
The coating composition of technical solution of the present invention prepare raw material include polysilazane, polysiloxanes, fluorine richness it is anti-
Dirty agent and colorant, the polysilazane and polysiloxanes can be copolymerized and generate polysilazane-polysiloxane copolymer, should
Polysilazane-polysiloxane copolymer has the advantages that hardness is high, adhesion is good and temperature tolerance is good, so that by the coating composition
The coating of formation has the advantages that hardness is high, adhesion is good and temperature tolerance is good.Also contain and the poly- silicon in the coating composition
The anti-fouling agent of the anti-fouling agent and colorant for the fluorine richness that azane-polysiloxane copolymer mixes, the fluorine richness can make by the coating
The coating that composition is formed has the advantages that easy to clean, which can make the coating as made from the coating composition also and have preferable
Appearance.Meanwhile polysilazane-the polysiloxane copolymer, the anti-fouling agent of fluorine richness and colorant are not admitted to venomous injurant
Matter, so that the coating as made from the coating composition also has the advantages that can reach food touch-safe rank.
Specific embodiment
The following is a clear and complete description of the technical scheme in the embodiments of the invention, it is clear that described embodiment
Only a part of the embodiments of the present invention, instead of all the embodiments.Based on the embodiments of the present invention, this field is common
Technical staff's every other embodiment obtained without creative efforts belongs to the model that the present invention protects
It encloses.
It is to be appreciated that the directional instruction (such as up, down, left, right, before and after ...) of institute is only used in the embodiment of the present invention
In explaining relative positional relationship, motion conditions etc. between component each under a certain particular pose, if the particular pose occurs
When change, then directionality instruction also correspondingly changes correspondingly.
In addition, the description for being related to " first ", " second " etc. in the present invention is used for description purposes only, and should not be understood as referring to
Show or imply its relative importance or implicitly indicates the quantity of indicated technical characteristic." first ", " are defined as a result,
Two " feature can explicitly or implicitly include at least one of the features.In addition, the technical solution between each embodiment can
It to be combined with each other, but must be based on can be realized by those of ordinary skill in the art, when the combination of technical solution occurs
Conflicting or cannot achieve when, will be understood that the combination of this technical solution is not present, also not the present invention claims protection model
Within enclosing.
The present invention provides a kind of coating composition.
The coating composition prepares the anti-fouling agent and colorant that raw material includes polysilazane, polysiloxanes, fluorine richness, institute
State polysilazane and polysiloxanes be copolymerized generation polysilazane-polysiloxane copolymer, the fluorine richness it is antifouling
Agent and colorant are mixed with the polysilazane-polysiloxane copolymer.
The coating composition of technical solution of the present invention prepare raw material include polysilazane, polysiloxanes, fluorine richness it is anti-
Dirty agent and colorant, the polysilazane and polysiloxanes can be copolymerized and generate polysilazane-polysiloxane copolymer, should
Polysilazane-polysiloxane copolymer has the advantages that hardness is high, adhesion is good and temperature tolerance is good, so that by the coating composition
The coating of formation has the advantages that hardness is high, adhesion is good and temperature tolerance is good.Also contain and the poly- silicon in the coating composition
The anti-fouling agent of the anti-fouling agent and colorant for the fluorine richness that azane-polysiloxane copolymer mixes, the fluorine richness can make by the coating
The coating that composition is formed has the advantages that easy to clean, which can make the coating as made from the coating composition also and have preferable
Appearance.Meanwhile polysilazane-the polysiloxane copolymer, the anti-fouling agent of fluorine richness and colorant are not admitted to venomous injurant
Matter, so that the coating as made from the coating composition also has the advantages that can reach food touch-safe rank.
The range that the polysilazane accounts for the mass percent for preparing raw material is 7~50%, and the polysiloxanes accounts for
The range of the mass percent for preparing raw material is 3~40%, and the anti-fouling agent of the fluorine richness accounts for the matter for preparing raw material
Measure percentage range be 0.01~20%, the colorant account for the mass percent for preparing raw material range be 0.01~
5%.
In an embodiment of the present invention, the polysilazane account for the mass percent for preparing raw material range be 7~
50%.Preferably, it is 10~45% that the polysilazane, which accounts for the range of the mass percent for preparing raw material, more preferably
20~40%, further preferably 25~35%.
In an embodiment of the present invention, the polysiloxanes account for the mass percent for preparing raw material range be 3~
40%.Preferably, it is 5~30% that the polysiloxanes, which accounts for the range of the mass percent for preparing raw material, more preferably
10~25%, further preferably 15~25%.
In an embodiment of the present invention, the anti-fouling agent of the fluorine richness accounts for the range of the mass percent for preparing raw material
It is 0.01~20%.Preferably, the anti-fouling agent of the fluorine richness account for the mass percent for preparing raw material range be 0.1~
15%, more preferably 1~10%, further preferably 5~10%.
In an embodiment of the present invention, the colorant account for the mass percent for preparing raw material range be 0.01~
5%.Preferably, the colorant account for the mass percent for preparing raw material range be 0.1~5%, more preferably 1~
5%, further preferably 2~3%.
The range that the polysilazane of technical solution of the present invention accounts for the mass percent for preparing raw material is 7~50%, institute
Stating polysiloxanes and accounting for the range of the mass percent for preparing raw material is 3~40%, and the anti-fouling agent of the fluorine richness accounts for described
The range for preparing the mass percent of raw material is 0.01~20%, and the colorant accounts for the model of the mass percent for preparing raw material
Enclosing is 0.01~5%, and the polysilazane and polysiloxanes under above-mentioned content produce polysilazane-polysiloxanes of preferable content
Copolymer, anti-fouling agent and colorant and the polysilazane-polysiloxane copolymer of fluorine richness mix, the coating of excellent performance is made
Composition, so that the coating as obtained by the coating composition not only has, hardness is high, adhesion is good, easy to clean, temperature tolerance is good,
And the advantages of reaching food touch-safe rank, also there is preferable appearance.
The colorant is selected from white pigment, yellow colorant, orange pigment, black pigment, purple, brown colorant, green
At least one of color colorant, blue colorant, grey colorant and red colorant.
In technical solution of the present invention, colorant is contained in the coating composition, the colorant can be white pigment, yellow color
Material, orange pigment, black pigment, purple, brown colorant, green pigment, blue colorant, grey colorant or red colorant,
So as to which there is colorful appearance by coating obtained by the coating composition.
The white pigment is selected from stibium trioxide (Antimony white), barium sulfate (Barium sulfate), lithopone
(Lithopone), at least one of titanium white (Titanium white) and zinc white (Zinc white).
The yellow colorant is nickel titanate antimony (Nickel titanate antimony) and/or titanium chromium palm fibre (Chrome
titanium brown)。
The orange pigment is zinc-tin rutile (Rutile Tin Zinc).
The black pigment is black selected from copper-chrome black spinelle (Copper chromite black spinel), titanium
(Titanium black), manganese dioxide (MnO2), Ma Sihei (Mars black), ivory black (Ivory black) and carbon black
At least one of (Carbon black).
The purple is cobalt phosphate (Cobalt Phosphate).
The brown colorant is titanium manganese brown (Manganese antimony titanate brown) and/or zinc-iron chromium palm fibre
(Chromium iron zinc brown)。
The green pigment is cobalt green (Cobalt green), malachite (Malachite) and glauconite (Green
At least one of earth).
The blue colorant is selected from celestine (Ultramarine), cobalt blue (Cobalt blue), Egyptian blue (Egyptian
Blue), at least one of the Chinese blue (Han blue), chessy copper (Azurite) and yttrium indium manganese blue (YInMn blue).
The grey colorant is copper-chrome black spinelle (Copper chromite black spinel), titanium is black
(Titanium black), manganese dioxide (MnO2), Ma Sihei (Mars black), violet black (Vine black), ivory black
At least one of (Ivory black) and carbon black (Carbon black) and stibium trioxide (Antimony white), barium sulfate
In (Barium Sulfate), lithopone (Lithopone), titanium white (Titanium white) and zinc white (Zinc white)
At least one mixture, burnt ochre (Burnt sienna), Indian red (India can also further be added in the mixture
) and at least one of cobalt blue (Cobalt blue) Red.
The red colorant is selected from burnt sienna (Burnt Sienna), burnt ochre (Red ochre) and Indian red (India
At least one of Red).
The above-mentioned colorant of technical solution of the present invention can reach food touch-safe rank, so that the colorant is added to painting
After feed composition, which also can reach food touch-safe rank.
It should be understood that colorant can be selected according to actual needs, so that coating shows preferable appearance.
The anti-fouling agent of the fluorine richness is selected from methyl perfluoro amyl ketone, 1- methyl -3- trifluoromethyl -2-Pyrrolidone, 1H,
1H- perfluor -1- tetradecyl alchohol, 1- fluorine heptane, ten trifluorohexane -1- sulfonic acid potassium salts, perfluor pentane, [(4- fluorophenoxy) methyl]
Ethylene oxide, 2H- perfluor -5,8,11,14,17- pentamethyls -3,6,9,12,15,18- six oxa- heneicosanes, 2- (fluoroform
Base) ten difluoro hexane of -3- ethyoxyl, ten fluoro- 4- (pentafluoroethyl group) oxepane sulfonic acid potassium salts, 1,1,1,2,2,3,4,5,5,6,
6,6- ten two fluoro- 3,4- bis- (trifluoromethyl) hexanes, perfluor eicosane, 1H, 6H- perflexane, 1,7- difluoro heptane, 1,1,1,
2,2,3,3,4,5,5,6,6,6- ten trifluorohexanes, 1,1,2,2,5,5,6,6- pungent fluorine hexane, perfluor are to terpane, seven fluorine third
Alkane, PF 5070, perfluor (methyl decahydronaphthalenes), perfluoropolyether, perfluor -1- butane sulfonic acid, perflenapent, perfluor (methyl ring
Hexane), perfluor (2,2,3,3- 4-methyl-butane), perfluor -1- octane, perflexane, N- perfluor n-decane, perfluoro -1,2-
Dimethyl cyclohexane, perfluor pentadecane, Perfluorononane, Sonazoid, perfluor dodecane, the perfluor tetradecane, perfluor -2,7- bis-
Methyloctane, perfluor hexadecane, perfluor -2,3,5,6- tetramethyl-ring hexanes, perfluor tridecane, trifluoromethyl-cyclopentane, perfluor
Dimethylcyclobutane, (perfluoro hexyl) benzene, perfluor-(1,3,5- trimethylbenzene), perfluorobutyl ethane, perfluorobutyl ether, perfluor
Lignocerane, perfluoro hexyl ethane, perfluor tetraethyleneglycol dimethyl ether, perfluor -2- methybutane, perfluor are pungent to terpane, perfluor
Base ethane, 3- (perfluoro hexyl) propylene oxide, 3- (perfluoro hexyl) propylene oxide, 3- (2- perfluoro hexyl ethyoxyl) -1,2- ring
Ethylene Oxide, 3- (Sonazoid) -1,2- propylene oxide, 3- (perfluoro-n-octane) -1,2- propylene oxide, 1H, 1H- perfluor -1-
The tetradecane, 2H- perfluor 15- methyl -3,6- dioxanonane, 3- (perfluor -5- methylhexyl) -1,2- propylene oxide, 1H- perfluor
Pentane, 1- (perfluor-n- hexyl) dodecane, 1- (perfluor-n- octyl) tetradecane, 1H, 6H- perflexane, 1- (perfluor-n- oneself
Base) decane, 1H- perfluor -2,4,4,-trimethylpentane, 1H, 10H- perfluoro decane, 1H- perfluor -2,6- dimethyl heptane, 1- first
Base -4- (perfluoro-ethyl) toluene, 2H- perfluor (2- methylpentane), ethyl perfluorobutyl ether, 8- perfluoro decyl octane, perfluor are different
In butane, perfluorobutyl methyl ethers, perfluoro propene oxid, 2- trifluoromethyl perflenapent and 2H-3H- perflenapent at least
It is a kind of.
In technical solution of the present invention, containing the anti-fouling agent of fluorine richness in the coating composition, it can make by the Coating material composition
Coating obtained by object have the advantages that it is easy to clean, and the anti-fouling agent of above-mentioned fluorine richness not be poisonous and harmful substance so that
The coating composition can reach food touch-safe rank.
It should be noted that the anti-fouling agent of fluorine richness can also can realize the substance of same or similar function for other, this
It invents without limitation.
The structural formula of the polysilazane are as follows:Wherein, R1For hydrogen-based, alkane, cycloalkane, olefine, virtue
Base, alkoxy, alkyl siloxy or alkylamino radical, R2For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy, alkyl silicon
Oxygroup or alkylamino radical, R3For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy, alkyl siloxy or alkylamino radical.
The structural formula of the polysiloxanes are as follows:Wherein, R4For hydrogen-based, alkane, cycloalkane, olefine,
Aryl, alkoxy or alkyl siloxy, R5For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy or alkyl silicon oxygen
Base.
It should be understood that the polysilazane and polysiloxanes are heat-resisting material.
It should be understood that R1、R2And R3It can be adjusted according to actual needs for identical group or in different groups
Section.
It should be understood that R4And R5It can be adjusted according to actual needs for identical group or in different groups.
It should be noted that R1、R2And R3The group of same or similar function, the present invention couple can also can be realized for other
This is with no restrictions;R4And R5The group of same or similar function can also can be realized for other, the present invention is without limitation.
In technical solution of the present invention, the polysilazane can be copolymerized with the polysiloxanes, generate the painting
The matrix resin of feed composition, so that the coating as obtained by the coating composition has, hardness is high, adhesion is good, temperature tolerance
It is good and the advantages of reach food touch-safe rank.
The molecular weight of the polysilazane is 100~1000.
The molecular weight of the polysiloxanes is 100~1300.
In one embodiment of the invention, the molecular weight of the polysilazane is 100,200,300,400,500,600,700,
800,900 or 1000.
In one embodiment of the invention, the molecular weight of the polysilazane is preferably 100~700, more preferably 100~
300。
In one embodiment of the invention, the molecular weight of the polysiloxanes is 100,200,300,400,500,600,700,
800,900,1000,1100,1200 or 1300.
In one embodiment of the invention, the molecular weight of the polysiloxanes is preferably 200~900, more preferably 200~
500。
The molecular weight of the polysilazane of technical solution of the present invention is 100~1000, the molecular weight of polysiloxanes is 100~
1300, after the polysiloxanes that the polysilazane and molecular weight that molecular weight is 100~1000 are 100~1300 is copolymerized,
Polysilazane-polysiloxane copolymer is produced, polysilazane-polysiloxane copolymer coating composition will be contained
After substrate forms coating, which has preferable hardness, adhesion and temperature tolerance.
The raw material for preparing of the coating composition further includes solvent, and the solvent accounts for the mass percent for preparing raw material
Range be 10~66%, preferably 15~50%, more preferably 20~40%, further preferably 30~35%.
The solvent can be selected from least one in alkane solvents, ether solvent, ketones solvent and benzenesulfonamide derivative species solvent
Kind.
The alkane solvents can be selected from n-hexane, normal octane, n-decane, chloroform, methylene chloride, dichloroethylene,
And at least one of mineral oil.
The ether solvent can be selected from least one of ether, petroleum ether and butyl oxide.
The ketones solvent can be selected from least one of acetone, methyl ethyl ketone, cyclohexanone and isophorone.
The benzenesulfonamide derivative species solvent in toluene, meta-xylene, paraxylene, ortho-xylene and chlorobenzene at least
It is a kind of.
It should be noted that the solvent of other anti-fouling agents that can dissolve polysiloxanes and polysilazane copolymers and fluorine richness
Also it can be used as solvent of the invention, the present invention is without limitation.
The anti-fouling agent of the polysilazane-polysiloxane copolymer and fluorine richness dissolves in solvent, so that the coating
Composition can relatively easily be coated on the surface of substrate, and have the effect of antifouling, easy to clean.
The raw material for preparing of the coating composition further includes catalyst, and the catalyst accounts for the quality hundred for preparing raw material
The range for dividing ratio is 0.01~5%, preferably 0.1~5%, more preferably 1~5%, further preferably 2~3%.
The catalyst is amines catalyst and/or metal-based catalysts.
The amines catalyst can be selected from fatty amine, cycloaliphatic amines, one of hydramine and aromatic amine or a variety of.
The fatty amine can be selected from least one of diethylamine, triethylamine and triethylene tetramine.
The cycloaliphatic amines can be selected from least one of triethylenediamine, piperazine, piperidines and morpholine.
The hydramine can be selected from N, N- dimethylethanolamine, diisopropanolamine (DIPA) and N, in N- diethyl ethylene diamine at least
It is a kind of.
The aromatic amine is selected from least one of aniline, o-phenylenediamine, benzidine and n,N-Dimethylaniline.
The metal-based catalysts can be organotin catalysts and/or palladium class catalyst.
The organotin catalysts can be selected from dibutyltindilaurylmercaptide cinnamic acid rouge, stannous octoate, stannous methide and triphenyltin
At least one of.
The palladium class catalyst can be selected from carbon/palladium, palladium chloride, propionic acid palladium salt, acetic acid palladium salt and triphenyl phosphorus palladium extremely
Few one kind.
It should be noted that other catalyst with similar performance also can be used as catalyst of the invention, the present invention couple
This is with no restrictions.
The catalyst can accelerate the copolyreaction between polysilazane and polysiloxanes, to generate institute in a short time
State polysilazane-polysiloxane copolymer.
The raw material for preparing of the coating composition further includes filler, and the filler accounts for the mass percent for preparing raw material
Range be 1~50%, preferably 5~40%, preferably 10~30%, more preferably 15~25%.
The filler is selected from silicon carbide, aluminium oxide, titanium oxide, zinc oxide, magnesia, aluminium hydroxide, white carbon black (titanium dioxide
Silica aerogel), concave convex rod, kaolin, bentonite, at least one of glass microsphere and ceramic microsphere.
The partial size of the filler may be less than 3 microns, it is preferable that less than 2 microns, more preferably 1 micron.
In an embodiment of the present invention, the range of the partial size of the filler is 0.2~0.8 micron.It should be understood that described
The partial size of filler is 0.2 micron, 0.3 micron, 0.4 micron, 0.5 micron, 0.6 micron, 0.7 micron or 0.8 micron.
It should be understood that filler can be uniformly dispersed when setting 0.2~0.8 micron for the particle size range of the filler
In coating composition, and make coating surface obtained more smooth.
In an alternative embodiment of the invention, the range of the partial size of the filler is 0.2~0.5 micron, more flat to obtain
Whole coating.
In an embodiment of the present invention, grinder can be used to grind filler, to reduce the partial size of filler.
In an alternative embodiment of the invention, which can be ground, to reduce the coating composition
In filler partial size.
In an embodiment of the present invention, it is scattered in coating composition to the uniform filling.
In technical solution of the present invention, the filler is selected from silicon carbide, aluminium oxide, titanium oxide, zinc oxide, magnesia, hydrogen-oxygen
Change in aluminium, white carbon black (aerosil), concave convex rod, kaolin, bentonite, glass microsphere and ceramic microsphere at least
One kind, to improve hardness, adhesion and the temperature tolerance of the coating as obtained by the coating composition.
It should be noted that other fillers with high temperature resistance also can be used as filler of the invention, the present invention is to this
With no restrictions.
It should be understood that solvent of the invention, catalyst and filler are also not admitted to poisonous and harmful substance, so that by the painting
Coating made from feed composition also has the advantages that food touch-safe.
In an embodiment of the present invention, the raw material for preparing of the coating composition includes: polysiloxanes, polysilazane, fluorine
Modified anti-fouling agent, filler, solvent, colorant and catalyst.Wherein, the polysiloxanes and polysilazane, which account for, described prepares raw material
Mass percent range be 10%~80%, the anti-fouling agent of the fluorine richness accounts for the mass percent range for preparing raw material
It is 0.01~15%, it is 1~50% that the filler, which accounts for the mass percent range for preparing raw material, and the solvent accounts for the system
The mass percent range of standby raw material is 10~66%, and it is 0.01 that the colorant, which accounts for the mass percent range for preparing raw material,
~5%, it is 0.01~5% that the catalyst, which accounts for the mass percent range for preparing raw material,.
In an alternative embodiment of the invention, the coating composition prepare raw material include: polysiloxanes, polysilazane,
Anti-fouling agent, filler, solvent, colorant and the catalyst of fluorine richness.Wherein, it is former to account for the preparation for the polysiloxanes and polysilazane
The mass percent range of material is 10%~60%, and the anti-fouling agent of the fluorine richness accounts for the mass percent model for preparing raw material
Enclosing is 0.01~20%, and it is 1~50% that the filler, which accounts for the mass percent range for preparing raw material, and the solvent accounts for described
The mass percent range for preparing raw material is 10~66%, and the colorant accounts for the mass percent range for preparing raw material and is
0.01~5%, it is 0.01~5% that the catalyst, which accounts for the mass percent range for preparing raw material,.
In still another embodiment of the process, the coating composition prepare raw material include: polysiloxanes, polysilazane,
Anti-fouling agent, filler, solvent, colorant and the catalyst of fluorine richness.Wherein, it is former to account for the preparation for the polysiloxanes and polysilazane
The mass percent range of material is 10%~60%, and the anti-fouling agent of the fluorine richness accounts for the mass percent model for preparing raw material
Enclosing is 0.01~15%, and it is 1~50% that the filler, which accounts for the mass percent range for preparing raw material, and the solvent accounts for described
The mass percent range for preparing raw material is 10~66%, and the colorant accounts for the mass percent range for preparing raw material and is
0.01~5%, it is 0.01~5% that the catalyst, which accounts for the mass percent range for preparing raw material,.
The present invention also provides a kind of preparation methods of coating composition, comprising the following steps:
Offer prepares raw material, described to prepare the anti-fouling agent and colorant that raw material includes polysilazane, polysiloxanes, fluorine richness;
Mixing polysilazane and polysiloxanes, polysilazane and polysiloxanes are copolymerized, and it is poly- to generate polysilazane-
Silicone copolymers;
The anti-fouling agent and colorant of fluorine richness are added into the polysilazane-polysiloxane copolymer, it is stirred, is made
The coating composition.
In an embodiment of the present invention, the polysilazane account for the mass percent for preparing raw material range be 7~
50%, the range that the polysiloxanes accounts for the mass percent for preparing raw material is 3~40%, the anti-fouling agent of the fluorine richness
The range for accounting for the mass percent for preparing raw material is 0.01~20%, and the colorant accounts for the quality percentage for preparing raw material
The range of ratio is 0.01~5%.
In an embodiment of the present invention, polysiloxanes and polysilazane can be placed in reactor, to polysiloxanes and poly- silicon
Azane carries out first time stir process so that polysiloxanes is uniformly mixed with polysilazane, and polysiloxanes can occur with polysilazane
Copolyreaction generates polysiloxanes-polysilazane copolymers.
In the present invention one is implemented, the stirring rate of the first time stir process is 100~800 revs/min, preferably
200~600 revs/min, more preferably 400~500 revs/min.
It should be understood that the time of the copolyreaction can be 10 seconds~50 minutes, can need to adjust according to actual production
The time of whole copolyreaction.
It should be noted that the stirring rate of the first time stir process and the time of copolyreaction can be also other numbers
Value, the present invention are without limitation.
The coating composition of technical solution of the present invention prepare raw material include polysilazane, polysiloxanes, fluorine richness it is anti-
Dirty agent and colorant, the polysilazane and polysiloxanes can be copolymerized and generate polysilazane-polysiloxane copolymer, should
Polysilazane-polysiloxane copolymer has the advantages that hardness is high, adhesion is good and temperature tolerance is good, so that by the coating composition
The coating of formation has the advantages that hardness is high, adhesion is good and temperature tolerance is good.Also contain and the poly- silicon in the coating composition
The anti-fouling agent of the anti-fouling agent and colorant for the fluorine richness that azane-polysiloxane copolymer mixes, the fluorine richness can make by the coating
The coating that composition is formed has the advantages that easy to clean, which can make the coating as made from the coating composition also and have preferable
Appearance.Meanwhile polysilazane-the polysiloxane copolymer, the anti-fouling agent of fluorine richness and colorant are not admitted to venomous injurant
Matter, so that the coating as made from the coating composition also has the advantages that can reach food touch-safe rank.
After mixing polysilazane and polysiloxanes, the preparation method of the coating composition further include: to polysilazane and
The step of catalyst is added in polysiloxanes.
The raw material for preparing of the coating composition further includes catalyst, and the catalyst accounts for the quality hundred for preparing raw material
The range for dividing ratio is 0.01~5%, preferably 0.1~5%, more preferably 1~5%, further preferably 2~3%.
The catalyst is amines catalyst and/or metal-based catalysts.
It should be understood that second of stir process is carried out to it after catalyst is added into polysilazane and polysiloxanes,
So that polysilazane, polysiloxanes and catalyst are uniformly mixed.
In an embodiment of the present invention, the stirring rate of second of stir process can be 1000~2000 revs/min, excellent
It is selected as 1200~1800 revs/min, more preferably 1500~1600 revs/min.
In an embodiment of the present invention, the time of second of stir process can be 10 seconds~50 minutes, preferably 5~
15 minutes, more preferably 8~12 minutes.
It should be noted that the time of the stirring rate of second of stir process and second of stir process can also be
Other numerical value, the present invention are without limitation.
In the technical solution of the present invention, catalyst can be added, to promote polysiloxanes to be copolymerized with polysilazane,
Matrix resin, i.e. polysiloxanes-polysilazane copolymers needed for generating the present invention.
After generating polysilazane-polysiloxane copolymer, before obtaining the coating composition, the system of the coating composition
Preparation Method further include: the step of solvent is added into polysilazane-polysiloxane copolymer.
The range that the solvent accounts for the mass percent for preparing raw material is 10~66%, preferably 15~50%, more
Add preferably 20~40%, further preferably 30~35%.
The solvent can be selected from least one in alkane solvents, ether solvent, ketones solvent and benzenesulfonamide derivative species solvent
Kind.
In technical solution of the present invention, the anti-fouling agent of the polysilazane-polysiloxane copolymer and fluorine richness dissolves in molten
In agent, so that the coating composition can relatively easily be coated on the surface of substrate.The filler and colorant are also dispersible in described
In the anti-fouling agent of solvent and polysilazane-polysiloxane copolymer and fluorine richness, to increase the hardness, attached of the coating composition
Property and temperature tolerance.
After generating polysilazane-polysiloxane copolymer, before obtaining the coating composition, the system of the coating composition
Preparation Method further include: the step of filler is added into polysilazane-polysiloxane copolymer.
The range that the filler accounts for the mass percent for preparing raw material is 1~50%, preferably 5~40%, preferably
It is 10~30%, more preferably 15~25%.
The filler can be selected from silicon carbide, aluminium oxide, titanium oxide, zinc oxide, magnesia, aluminium hydroxide, white carbon black, bumps
At least one of stick, kaolin, bentonite, glass microsphere and ceramic microsphere.
In an embodiment of the present invention, solvent, colorant, filler and fluorine are added into polysilazane-polysiloxane copolymer
After modified anti-fouling agent, third time stir process can be carried out to it, so as to polysilazane-polysiloxane copolymer, solvent and fill out
Material is uniformly mixed.
It should be understood that the antifouling of solvent and fluorine richness can be first added into the polysilazane-polysiloxane copolymer
Agent adds filler and colorant, carries out third time stir process to it.It can also be total to the polysilazane-polysiloxanes simultaneously
The anti-fouling agent of solvent, colorant, filler and fluorine richness is added in polymers, third time stir process is carried out to it.It can also be first to described
After solvent is added in polysilazane-polysiloxane copolymer, the anti-fouling agent of filler, colorant and fluorine richness is added, it is carried out
Third time stir process.
The stirring rate of the third time stir process can be 100~3000 revs/min, preferably 500~2000 revs/min
Clock, more preferably 1000~1500 revs/min.
In an embodiment of the present invention, the time of the third time stir process can be 2~20 minutes, preferably 5~15
Minute, more preferably 8~12 minutes.
It should be noted that the stirring rate of the third time stir process and the time of third time stir process can also be
Other numerical value, the present invention are without limitation.
The partial size of the filler may be less than 3 microns, it is preferable that less than 2 microns, more preferably 1 micron.
In an embodiment of the present invention, the range of the partial size of the filler is 0.2~0.8 micron.It should be understood that described
The partial size of filler is 0.2 micron, 0.3 micron, 0.4 micron, 0.5 micron, 0.6 micron, 0.7 micron or 0.8 micron.
It should be understood that filler can be uniformly dispersed when setting 0.2~0.8 micron for the particle size range of the filler
In coating composition, and make coating surface obtained more smooth.
In an alternative embodiment of the invention, the range of the partial size of the filler is 0.2~0.5 micron, more flat to obtain
Whole coating.
In an embodiment of the present invention, grinder can be used to grind filler, to reduce the partial size of filler, then will be through
Filler after milled processed is added into polysilazane-polysiloxane copolymer.
In an alternative embodiment of the invention, directly the biggish filler of partial size can be added total to polysilazane-polysiloxanes
In in polymers, then the coating head product is ground, to reduce the partial size of the filler in the coating composition.
The time of the milled processed can be 0.5~1 hour.Milling time can be adjusted according to actual needs, to obtain
The filler of corresponding partial size.
It should be noted that other fillers with high temperature resistance also can be used as filler of the invention, the present invention is to this
With no restrictions.
It should also be noted that, in the preparation method of the coating composition, the order of addition and lapping mode of each component
It can be adjusted and select according to actual needs, and when the time of above-mentioned copolyreaction, mixing speed, mixing time, grinding
Between it is equal be representative value in preparation process, can be adjusted according to actual needs.
It should be understood that can be ground to the coating composition, to reduce each component in the coating composition
Partial size.
The present invention also provides a kind of coating piece, the coating piece includes matrix and the coating for being formed in matrix surface, described
Contain the coating composition in coating.
It should be understood that the coating can be formed by the coating composition in matrix surface.
It should be understood that the thermal weight loss in 500 DEG C of oxygen atmosphere of the coating as obtained by the coating composition is less than
5%, show that the coating has very excellent heat resistance.
Component, proportion, preparation method of the coating composition etc. please refer to above-described embodiment, since this coating piece uses
Whole technical solutions of above-mentioned all embodiments, thus it is at least all beneficial brought by the technical solution with above-described embodiment
Effect, this is no longer going to repeat them.
The range of the thickness of the coating is 1~100 micron, and preferably 5~60 microns, more preferably 10~50 is micro-
Rice, further preferably 20~30 microns.
It should be understood that the thickness of the coating can be adjusted according to actual demand.
The thickness of the coating can be 1 micron, 2 microns, 5 microns, 10 microns, 20 microns, 50 microns or 100 microns.
In technical solution of the present invention, the range of the thickness of the coating can be 1~100 micron, be formed in the surface of matrix
After the coating of above-mentioned thickness, which can be effectively protected matrix so that the coating piece have hardness height, high temperature resistant,
It is easy to clean, adhesion is good, reaches the advantages that food touch-safe rank.
The present invention also provides a kind of preparation methods of coating piece, comprising the following steps:
Matrix and the coating composition are provided;
By the coating composition in the surface of matrix, the coating piece is made.
It should be understood that can be first ground to the coating composition, reunited with reducing, then will be after reunion is handled
Coating composition in the surface of matrix.
It should be understood that the coating composition heats matrix when the surface of matrix, should add
The temperature of heat treatment is lower than 300 DEG C, preferably 100 DEG C~280 DEG C, more preferably 120~150 DEG C, so that matrix surface
Curing of coating composition forms coating.The range of the thickness of the coating can be 1~100 micron.
In an embodiment of the present invention, pre-treatment can be carried out to matrix, the pre-treatment can be oil removing, cleaning and drying
Deng improving coating in the adhesive force of matrix surface so that matrix surface is clean.
In the inventive solutions, can directly consolidate in the surface of matrix to coating composition coating composition
It can be prepared by the coating piece after change, so that the preparation method of coating piece of the invention has the advantages that moulding process is simple.And
And the temperature of the curing process is lower than 300 DEG C, the cured technical solution of high temperature compared to the prior art, coating piece of the invention
Preparation method also have the advantages that energy consumption it is low.
It should be understood that do not need to carry out the pre-treatments such as sanding to substrate since the coating has preferable adhesion,
Reduce the technology difficulty of the preparation method of the coating piece, and compared to the prior art in need to substrate carry out sanding processing
Technical solution, the preparation method of coating piece of the invention also has the advantages that environmental protection.
The present invention also provides a kind of household electrical appliance, the household electrical appliance include the coating piece.
The household electrical appliance can be micro-wave oven, electromagnetic oven, oven, bread producing machine, flour stranding machine, smoke exhaust ventilator or refrigerator etc..
In an embodiment of the present invention, the coating piece can be the shell of household electrical appliance.Specifically, which can be family
The shell or inner casing of electrical appliance.
In a specific embodiment of the invention, when the household electrical appliance are micro-wave oven or oven, the coating piece is also
It can be micro-wave oven or the shell or heating dish of oven.
The specific structure of the household electrical appliance please refers to above-described embodiment, since this household electrical appliance uses above-mentioned all implementations
Whole technical solutions of example, therefore at least all beneficial effects brought by the technical solution with above-described embodiment, herein not
It repeats one by one again.
It should be understood that the raw material for preparing of the coating composition is not domestic and international object regulation limitation or be forbidden to use
Matter, and in the preparation process of the coating composition and in the preparation process of the coating piece, nuisance will not be generated
Matter, so that the advantages of coating composition, coating, coating piece and electronic device all have safety and environmental protection.
The following are several embodiments of the preparation method of coating composition of the present invention:
Embodiment 1
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 40%;
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 35%;
Perfluor pentane, the range for accounting for the mass percent for preparing raw material is 20%;
Copper-chrome black spinelle, the range for accounting for the mass percent for preparing raw material is 5%;
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 350 revs/min of speed
Alkane, the copolyreaction between polysiloxanes and polysilazane generate polysiloxanes-polysilazane copolymers;And
Perfluor pentane and copper-chrome black spinelle are added into the polysiloxanes-polysilazane copolymers, with 2000 turns/
The speed of minute is stirred, and obtains coating composition.
Embodiment 2
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For aryl, R2For hydrogen-based, R3For alkylamino radical, the polysilazane accounts for described
The range for preparing the mass percent of raw material is 35%;
Polysiloxanes, the R of the polysiloxanes4For cycloalkane, R5For alkyl siloxy, the polysiloxanes accounts for the system
The range of the mass percent of standby raw material is 20%;
2H- perfluor -5,8,11,14,17- pentamethyls -3,6,9,12,15,18- six oxa- heneicosanes account for the system
The range of the mass percent of standby raw material is 15%;
Butyl oxide, the range for accounting for the mass percent for preparing raw material is 20%;
Cyclohexanone, the range for accounting for the mass percent for preparing raw material is 7%;
Barium sulfate, the range for accounting for the mass percent for preparing raw material is 3%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 550 revs/min of speed
Alkane, the copolyreaction between polysiloxanes and polysilazane generate polysiloxanes-polysilazane copolymers;And
Addition butyl oxide, cyclohexanone and 2H- perfluor -5,8 into the polysiloxanes-polysilazane copolymers, 11,14,
17- pentamethyl -3,6 after 9,12,15,18- six oxa- heneicosanes, adds barium sulfate, with 2000 revs/min of speed into
Row stirring, obtains coating composition.
Embodiment 3
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For olefine, R2For alkylsiloxane, R3For alkane, the polysilazane
The range for accounting for the mass percent for preparing raw material is 33%;
Polysiloxanes, the R of the polysiloxanes4For alkane, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 17%;
1,1,1,2,2,3,4,5,5,6,6,6- ten two fluoro- 3,4- bis- (trifluoromethyl) hexane accounts for and described prepares raw material
Mass percent range be 13%;
Toluene, the range for accounting for the mass percent for preparing raw material is 7%;
Isophorone, the range for accounting for the mass percent for preparing raw material is 4%;
Aluminium oxide, the range for accounting for the mass percent for preparing raw material is 10%, the model of the partial size of the aluminium oxide
Enclose is 2.6~3.3 microns;
Silicon carbide, the range for accounting for the mass percent for preparing raw material is 10%, the model of the partial size of the silicon carbide
Enclose is 2.5~3.6 microns;
Stannous methide, the range for accounting for the mass percent for preparing raw material is 3%;
Manganese dioxide, the range for accounting for the mass percent for preparing raw material is 3%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 350 revs/min of speed
Alkane;
Stannous methide is added into the polysiloxanes and polysilazane, is stirred with 1900 revs/min of speed, two
Methyl tin can promote the copolyreaction between polysiloxanes and polysilazane, generate polysiloxanes-polysilazane copolymers;
The addition toluene, isophorone and 1 into the polysiloxanes-polysilazane copolymers, 1,1,2,2,3,4,5,5,
After 6,6,6- ten two fluoro- 3,4- bis- (trifluoromethyl) hexanes, aluminium oxide, silicon carbide and manganese dioxide are added, with 2800 revs/min
The speed of clock is stirred, and obtains coating head product;And
Coating head product is ground, keeps the range 0.21~0.45 of the partial size of aluminium oxide and silicon carbide micro-
Rice obtains coating composition.
Embodiment 4
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For cycloalkane, R3For hydrogen-based, the polysilazane accounts for described
The range for preparing the mass percent of raw material is 30%;
Polysiloxanes, the R of the polysiloxanes4For alkylamino radical, R5For alkoxy, it is former that the polysiloxanes accounts for the preparation
The range of the mass percent of material is 15%;
1,1,1,2,2,3,3,4,5,5,6,6,6- ten trifluorohexane accounts for the model of the mass percent for preparing raw material
Enclose is 15%;
Ortho-xylene, the range for accounting for the mass percent for preparing raw material is 6%;
Petroleum ether, the range for accounting for the mass percent for preparing raw material is 3%;
Aluminium oxide, the range for accounting for the mass percent for preparing raw material is 11%, the model of the partial size of the aluminium oxide
Enclose is 2.1~3 microns;
White carbon black, the range for accounting for the mass percent for preparing raw material is 15%, the model of the partial size of the white carbon black
Enclose is 2.2~3 microns;
Acetic acid palladium salt, the range for accounting for the mass percent for preparing raw material is 2%;
Lithopone, the range for accounting for the mass percent for preparing raw material is 3%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 660 revs/min of speed
Alkane;
Acetic acid palladium salt is added into the polysiloxanes and polysilazane, is stirred with 1300 revs/min of speed, second
Sour palladium salt can promote the copolyreaction between polysiloxanes and polysilazane, generate polysiloxanes-polysilazane copolymers;
The addition ortho-xylene, petroleum ether and 1 into the polysiloxanes-polysilazane copolymers, 1,1,2,2,3,3,4,
After 5,5,6,6,6- ten trifluorohexanes, aluminium oxide, white carbon black and lithopone are added, is stirred with 1600 revs/min of speed
It mixes, obtains coating head product;And
Coating head product is ground, keeps the range 0.21~0.35 of the partial size of aluminium oxide and white carbon black micro-
Rice obtains coating composition.
Embodiment 5
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For alkylamino radical, R2For alkyl, R3For aryl, the polysilazane accounts for described
The range for preparing the mass percent of raw material is 28%;
Polysiloxanes, the R of the polysiloxanes4For alkylsiloxane, R5For cycloalkane, the polysiloxanes accounts for the system
The range of the mass percent of standby raw material is 12%;
Perfluor -1- butane sulfonic acid, the range for accounting for the mass percent for preparing raw material is 11%;
N-hexane, the range for accounting for the mass percent for preparing raw material is 10%;
Acetone, the range for accounting for the mass percent for preparing raw material is 12%;
Concave convex rod, the range for accounting for the mass percent for preparing raw material is 4%, the range of the partial size of the concave convex rod
It is 2.5~3 microns;
White carbon black, the range for accounting for the mass percent for preparing raw material is 4%, the range of the partial size of the white carbon black
It is 2~3.2 microns;
Magnesia, the range for accounting for the mass percent for preparing raw material is 14%, the model of the partial size of the magnesia
Enclose is 0.2~0.25 micron;
Triethylene tetramine, the range for accounting for the mass percent for preparing raw material is 2%;
Malachite, the range for accounting for the mass percent for preparing raw material is 3%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 750 revs/min of speed
Alkane;
Triethylene tetramine is added into the polysiloxanes and polysilazane, is stirred with 1400 revs/min of speed,
Triethylene tetramine can promote the copolyreaction between polysiloxanes and polysilazane, generate polysiloxanes-polysilazane copolymers;
After n-hexane, acetone and perfluor -1- butane sulfonic acid is added into the polysiloxanes-polysilazane copolymers, then
Concave convex rod, white carbon black, magnesia and malachite is added, is stirred with 2300 revs/min of speed, obtains coating head product;
And
Coating head product is ground, concave convex rod, 0.2~0.25 micron of range of partial size of white carbon black are made,
Obtain coating composition.
Embodiment 6
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For aryl, R2For aryl, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 25%;
Polysiloxanes, the R of the polysiloxanes4For olefine, R5For hydrogen-based, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 10%;
Perfluoro -1,2- dimethyl cyclohexane, the range for accounting for the mass percent for preparing raw material is 9%;
Methyl ethyl ketone, the range for accounting for the mass percent for preparing raw material is 8%;
Meta-xylene, the range for accounting for the mass percent for preparing raw material is 7%;
Aluminium oxide, the range for accounting for the mass percent for preparing raw material is 30%, the model of the partial size of the aluminium oxide
Enclose is 0.24~0.33 micron;And
Titanium oxide, the range for accounting for the mass percent for preparing raw material is 3%, the range of the partial size of the titanium oxide
It is 0.21~0.32 micron;
Bentonite, the range for accounting for the mass percent for preparing raw material is 3%, the range of the bentonitic partial size
It is 0.25~0.35 micron;
Triphenyltin, the range for accounting for the mass percent for preparing raw material is 2%;
Cobalt blue, the range for accounting for the mass percent for preparing raw material is 3%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 750 revs/min of speed
Alkane;
Triphenyltin is added into the polysiloxanes and polysilazane, is stirred with 1100 revs/min of speed, three
Phenyltin can promote the copolyreaction between polysiloxanes and polysilazane, generate polysiloxanes-polysilazane copolymers;And
Methyl ethyl ketone, meta-xylene and perfluoro -1,2- dimethyl are added into the polysiloxanes-polysilazane copolymers
After hexamethylene, aluminium oxide, titanium oxide, bentonite and cobalt blue are added, is stirred, is applied with 2300 revs/min of speed
Feed composition.
Embodiment 7
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For alkane, R2For alkane, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 23%;
Polysiloxanes, the R of the polysiloxanes4For alkoxy, R5For alkoxy, it is former that the polysiloxanes accounts for the preparation
The range of the mass percent of material is 7%;
Perfluor -2,7- dimethyl octane, the range for accounting for the mass percent for preparing raw material is 7%;
Toluene, the range for accounting for the mass percent for preparing raw material is 34%;
Aluminium oxide, the range for accounting for the mass percent for preparing raw material is 17%, the model of the partial size of the aluminium oxide
Enclose is 2.5~3 microns;
Zinc oxide, the range for accounting for the mass percent for preparing raw material is 5%, the range of the partial size of the zinc oxide
It is 2~3 microns;
Ceramic microsphere, the range for accounting for the mass percent for preparing raw material is 3%, the partial size of the ceramic microsphere
Range is 0.2~0.3 micron;
Acetic acid palladium salt, the range for accounting for the mass percent for preparing raw material is 2%;
Titanium manganese brown, the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 100 revs/min of speed
Alkane;
Acetic acid palladium salt is added into the polysiloxanes and polysilazane, is stirred with 1800 revs/min of speed, second
Sour palladium salt can promote the copolyreaction between polysiloxanes and polysilazane, generate polysiloxanes-polysilazane copolymers;
After toluene, perfluor -2,7- dimethyl octane is added into the polysiloxanes-polysilazane copolymers, add
Aluminium oxide, zinc oxide and titanium manganese brown, are stirred with 2700 revs/min of speed, obtain coating head product;And
Coating head product is ground, 0.2~0.25 micron of range of the partial size of aluminium oxide and zinc oxide is made,
Ceramic microsphere is added, coating composition is obtained.
Embodiment 8
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For olefine, R2For aryl, R3For hydrogen-based, the polysilazane accounts for described
The range for preparing the mass percent of raw material is 20%;
Polysiloxanes, the R of the polysiloxanes4For alkane, R5For alkane, the polysiloxanes accounts for the raw material for preparing
The range of mass percent is 5%;
Perfluor-(1,3,5- trimethylbenzene), the range for accounting for the mass percent for preparing raw material is 5%;
Ether, the range for accounting for the mass percent for preparing raw material is 21%;
Paraxylene, the range for accounting for the mass percent for preparing raw material is 20%;
White carbon black, the range for accounting for the mass percent for preparing raw material is 10%, the model of the partial size of the white carbon black
Enclose is 2.5~3 microns;
Aluminium hydroxide, the range for accounting for the mass percent for preparing raw material is 12%, the partial size of the aluminium hydroxide
Range be 2~3 microns;
Glass microsphere, the range for accounting for the mass percent for preparing raw material is 2%, the partial size of the glass microsphere
Range is 0.2~0.3 micron;
N,N-Dimethylaniline, the range for accounting for the mass percent for preparing raw material is 1%;
Cobalt phosphate, the range for accounting for the mass percent for preparing raw material is 4%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 550 revs/min of speed
Alkane;
N,N-Dimethylaniline is added into the polysiloxanes and polysilazane, is carried out with 1600 revs/min of speed
Stirring, n,N-Dimethylaniline can promote the copolyreaction between polysiloxanes and polysilazane, generate the poly- silicon nitrogen of polysiloxanes-
Alkyl copolymer;
Ether, paraxylene and perfluor-(1,3,5- trimethyl are added into the polysiloxanes-polysilazane copolymers
Benzene) after, white carbon black, aluminium hydroxide and cobalt phosphate are added, is stirred with 2200 revs/min of speed, coating primiparity is obtained
Object;And
Coating head product is ground, keeps the range 0.2~0.3 of the partial size of white carbon black and aluminium hydroxide micro-
Rice adds glass microsphere, obtains coating composition.
Embodiment 9
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 30%;
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 30%;
Perfluor tetraethyleneglycol dimethyl ether, the range for accounting for the mass percent for preparing raw material is 10%;
Butyl oxide, the range for accounting for the mass percent for preparing raw material is 23%;
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 3%;
Lithopone, the range for accounting for the mass percent for preparing raw material is 2%;
Titanium white, the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 250 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 1700 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;
Butyl oxide and perfluor tetraethyleneglycol dimethyl ether are added into the polysiloxanes-polysilazane copolymers, adds
Lithopone and titanium white are stirred with 2700 revs/min of speed, obtain coating composition.
Embodiment 10
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 40%;
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 20%;
Perfluor tetraethyleneglycol dimethyl ether, the range for accounting for the mass percent for preparing raw material is 10%;
Butyl oxide, the range for accounting for the mass percent for preparing raw material is 23%;
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 3%;
Titanium is black, and the range for accounting for the mass percent for preparing raw material is 3%;
Titanium white, the range for accounting for the mass percent for preparing raw material is 1%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 120 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 1400 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;And
After butyl oxide and perfluor tetraethyleneglycol dimethyl ether is added into the polysiloxanes-polysilazane copolymers, then plus
Enter that titanium is black and titanium white, is stirred with 2100 revs/min of speed, obtains coating composition.
Embodiment 11
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 20%;
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 40%;
Perfluor tetraethyleneglycol dimethyl ether, the range for accounting for the mass percent for preparing raw material is 10%;
Butyl oxide, the range for accounting for the mass percent for preparing raw material is 23%;
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 3%;
Nickel titanate antimony, the range for accounting for the mass percent for preparing raw material is 2%;
Titanium chromium palm fibre, the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 180 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 1400 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;
After butyl oxide and perfluor tetraethyleneglycol dimethyl ether is added into the polysiloxanes-polysilazane copolymers, then plus
Enter nickel titanate antimony and titanium chromium palm fibre, is stirred with 2400 revs/min of speed, obtains coating head product;And
It to the coating head product, is ground, obtains coating composition.
Embodiment 12
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 40%,
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 20%;
Perfluor tetraethyleneglycol dimethyl ether, the range for accounting for the mass percent for preparing raw material is 10%;
Butyl oxide, the range for accounting for the mass percent for preparing raw material is 18%;
Silicon carbide, the range for accounting for the mass percent for preparing raw material is 5%, the range of the partial size of the silicon carbide
It is 2.5~3 microns;
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 3%;
Ma Sihei, the range for accounting for the mass percent for preparing raw material is 2%;
Indian red, the range for accounting for the mass percent for preparing raw material is 1%;
Barium sulfate, the range for accounting for the mass percent for preparing raw material is 1%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 300 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 1300 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;
After butyl oxide and perfluor tetraethyleneglycol dimethyl ether is added into the polysiloxanes-polysilazane copolymers, then plus
Enter silicon carbide, Ma Sihei, Indian red and barium sulfate, be stirred with 2600 revs/min of speed, obtains coating head product;And
Coating head product is ground, 0.5~0.75 micron of range of the partial size of silicon carbide is made, obtains coating
Composition.
Embodiment 13
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 40%;
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 20%;
Perfluor tetraethyleneglycol dimethyl ether, the range for accounting for the mass percent for preparing raw material is 10%;
Butyl oxide, the range for accounting for the mass percent for preparing raw material is 18%;
Aluminium oxide, the range for accounting for the mass percent for preparing raw material is 5%, the range of the partial size of the aluminium oxide
It is 0.25~0.33 micron;
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 3%;
Stibium trioxide, the range for accounting for the mass percent for preparing raw material is 1%;
Barium sulfate, the range for accounting for the mass percent for preparing raw material is 1%;
Lithopone, the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 900 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 1200 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;
After butyl oxide and perfluor tetraethyleneglycol dimethyl ether is added into the polysiloxanes-polysilazane copolymers, then plus
Enter aluminium oxide, stibium trioxide, barium sulfate and lithopone, be stirred with 2500 revs/min of speed, obtains coating composition.
Embodiment 14
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 40%;
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 20%;
Perfluor tetraethyleneglycol dimethyl ether, the range for accounting for the mass percent for preparing raw material is 10%;
Butyl oxide, the range for accounting for the mass percent for preparing raw material is 18%;
Silicon carbide, the range for accounting for the mass percent for preparing raw material is 5%, the range of the partial size of the silicon carbide
It is 2~3 microns;And
Stannous methide, the range for accounting for the mass percent for preparing raw material is 3%;
Cobalt green, the range for accounting for the mass percent for preparing raw material is 1%;
Malachite, the range for accounting for the mass percent for preparing raw material is 1%;
Glauconite, the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 200 revs/min of speed
Alkane;
Stannous methide is added into the polysiloxanes and polysilazane, is stirred with 1100 revs/min of speed, two
Methyl tin can promote the copolyreaction between polysiloxanes and polysilazane, generate polysiloxanes-polysilazane copolymers;
After butyl oxide and perfluor tetraethyleneglycol dimethyl ether is added into the polysiloxanes-polysilazane copolymers, then plus
Enter silicon carbide, cobalt green, malachite and glauconite, be stirred with 2500 revs/min of speed, coating head product is made;
Coating head product is ground, 0.8~0.9 micron of range of the partial size of silicon carbide is made, obtains coating
Composition.
Embodiment 15
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For hydrogen-based, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 17%;
Polysiloxanes, the R of the polysiloxanes4For hydrogen-based, R5For olefine, the polysiloxanes, which accounts for, described prepares raw material
Mass percent range be 3%;
3- (2- perfluoro hexyl ethyoxyl) -1,2- propylene oxide, accounts for the range of the mass percent for preparing raw material
It is 3%;
Paraxylene, the range for accounting for the mass percent for preparing raw material is 48%;
Silicon carbide, the range for accounting for the mass percent for preparing raw material is 25%, the model of the partial size of the silicon carbide
Enclose is 0.2~0.3 micron;And
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 1%;
Burnt sienna, the range for accounting for the mass percent for preparing raw material is 1%;
Burnt ochre, the range for accounting for the mass percent for preparing raw material is 1%;
Indian red, the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 300 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 1600 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;
Paraxylene and 3- (2- perfluoro hexyl ethyoxyl) -1 are added into the polysiloxanes-polysilazane copolymers,
After 2- propylene oxide, burnt sienna, burnt ochre, Indian red and silicon carbide are added, is stirred with 2600 revs/min of speed,
Coating composition is made.
Embodiment 16
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For alkane, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 12%;
Polysiloxanes, the R of the polysiloxanes4For alkylamino radical, R5For olefine, it is former that the polysiloxanes accounts for the preparation
The range of the mass percent of material is 3%;
3- (2- perfluoro hexyl ethyoxyl) -1,2- propylene oxide, accounts for the range of the mass percent for preparing raw material
It is 3%;
Paraxylene, the range for accounting for the mass percent for preparing raw material is 54%;
Silicon carbide, the range for accounting for the mass percent for preparing raw material is 25%, the model of the partial size of the silicon carbide
Enclose is 1~2 micron;And
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 1%;
Ivory black, the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 400 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 1800 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;
Paraxylene and 3- (2- perfluoro hexyl ethyoxyl) -1 are added into the polysiloxanes-polysilazane copolymers,
After 2- propylene oxide, ivory black and silicon carbide are added, is stirred with 3000 revs/min of speed, coating head product is made;
Coating head product is ground, the range of the partial size of silicon carbide is made to reach 0.21~0.32 micron, is made
The coating composition.
Embodiment 17
The preparation method of the coating composition the following steps are included:
Offer prepares raw material, and the raw material for preparing includes:
Polysilazane, the R of the polysilazane1For hydrogen-based, R2For alkane, R3For hydrogen-based, the polysilazane accounts for the system
The range of the mass percent of standby raw material is 7%;
Polysiloxanes, the R of the polysiloxanes4For alkylamino radical, R5For olefine, it is former that the polysiloxanes accounts for the preparation
The range of the mass percent of material is 3%;
3- (2- perfluoro hexyl ethyoxyl) -1,2- propylene oxide, accounts for the range of the mass percent for preparing raw material
It is 3%;
Paraxylene, the range for accounting for the mass percent for preparing raw material is 59%;
Silicon carbide, the range for accounting for the mass percent for preparing raw material is 25%, the model of the partial size of the silicon carbide
Enclose is 1~2 micron;And
Triethylenediamine, the range for accounting for the mass percent for preparing raw material is 1%;
The Chinese is blue, and the range for accounting for the mass percent for preparing raw material is 2%.
Polysilazane and polysiloxanes are placed in reactor, polysilazane and poly- silicon oxygen are mixed with 450 revs/min of speed
Alkane;
Triethylenediamine is added into the polysiloxanes and polysilazane, is stirred with 2000 revs/min of speed
It mixes, triethylenediamine can promote the copolyreaction between polysiloxanes and polysilazane, and it is total to generate polysiloxanes-polysilazane
Polymers;
Paraxylene and 3- (2- perfluoro hexyl ethyoxyl) -1 are added into the polysiloxanes-polysilazane copolymers,
After 2- propylene oxide, adds silicon carbide and the Chinese is blue, be stirred with 3000 revs/min of speed, coating head product is made;
Coating head product is ground, the range of the partial size of silicon carbide is made to reach 0.2~0.3 micron, institute is made
State coating composition.
By the coating composition as obtained by above-described embodiment 1-17 in substrate, coating is formed, sample is obtained, can order
Entitled sample 1, sample 2..... sample 17, to the hardness of the coating of sample 1-17, adhesion temperature tolerance and water contact angle into
Row test, test result please join table 1.
The physical property measurement result of 1 coating of table
The hardness of sample 1-17 is tested according to GB/T 6739-1996 (hardness of film method of testing), shows sample 1-
The range of 17 hardness is 6~9H, shows that sample 1-17 all has preferable hardness.
The adhesion of sample 1-17 is tested according to GB/T 9286 (adhesive force method of testing), display sample 1-17's
The attachment of hundred lattice can reach 0 grade, show that the adhesion of sample 1-17 is also preferable.
The weightlessness of sample 1-17 is tested according to GB/T 9286 (temperature tolerance test method), display sample 1-17's is resistance to
Warm nature is also preferable.
It is tested using water contact angle of the shape image analysis method to sample 1-17, the water contact angle of sample 1-17 is big
In 90 °, show the advantages of sample 1-17 all has easy cleaning.
The above is only a preferred embodiment of the present invention, is not intended to limit the scope of the invention, all in the present invention
Inventive concept under, using equivalent structure transformation made by present specification, be applied directly or indirectly in other phases
The technical field of pass is included in scope of patent protection of the invention.
Claims (25)
1. a kind of coating composition, which is characterized in that the raw material for preparing of the coating composition includes polysilazane, poly- silicon oxygen
The anti-fouling agent and colorant of alkane, fluorine richness, the polysilazane and polysiloxanes are copolymerized generation polysilazane-poly- silicon oxygen
Alkyl copolymer, the anti-fouling agent and colorant of the fluorine richness are mixed with the polysilazane-polysiloxane copolymer.
2. coating composition as described in claim 1, which is characterized in that the polysilazane accounts for the quality for preparing raw material
The range of percentage is 7~50%, and the range that the polysiloxanes accounts for the mass percent for preparing raw material is 3~40%,
The range that the anti-fouling agent of the fluorine richness accounts for the mass percent for preparing raw material is 0.01~20%, and the colorant accounts for described
The range for preparing the mass percent of raw material is 0.01~5%.
3. coating composition as described in claim 1, which is characterized in that the colorant is selected from white pigment, yellow colorant, orange
In color colorant, black pigment, purple, brown colorant, green pigment, blue colorant, grey colorant and red colorant extremely
Few one kind.
4. coating composition as claimed in claim 3, which is characterized in that the white pigment is selected from stibium trioxide, barium sulfate, zinc barium
At least one of white, titanium white and zinc white;And/or
The yellow colorant is nickel titanate antimony and/or titanium chromium palm fibre;And/or
The orange pigment is zinc-tin rutile;And/or
The black pigment is selected from copper-chrome black spinelle, titanium is black, at least one in manganese dioxide, Ma Sihei, ivory black and carbon black
Kind;And/or
The purple is cobalt phosphate;And/or
The brown colorant is titanium manganese brown and/or zinc-iron chromium palm fibre;And/or
The green pigment is selected from least one of cobalt green, malachite and glauconite;And/or
The blue colorant is selected from least one of celestine, cobalt blue, Egyptian blue, Chinese indigo plant, chessy copper and yttrium indium manganese indigo plant;And/
Or,
The grey colorant be black copper-chrome black spinelle, titanium, manganese dioxide, Ma Sihei, violet black, in ivory black and carbon black extremely
The mixture or the grey colorant of at least one of few a kind of and stibium trioxide, barium sulfate, lithopone, titanium white and zinc white are copper
Chrome black spinelle, titanium be black, at least one of manganese dioxide, Ma Sihei, violet black, ivory black and carbon black, with stibium trioxide, barium sulfate,
The mixture of at least one of lithopone, titanium white and zinc white and at least one of burnt ochre, Indian red and cobalt blue;And/
Or,
The red colorant is selected from least one of burnt sienna, burnt ochre and Indian red.
5. coating composition as described in claim 1, which is characterized in that the anti-fouling agent of the fluorine richness is selected from methyl perfluoro penta
Base ketone, 1- methyl -3- trifluoromethyl -2-Pyrrolidone, 1H, 1H- perfluor -1- tetradecyl alchohol, 1- fluorine heptane, ten trifluorohexane -1-
Sulfonic acid potassium salt, perfluor pentane, [(4- fluorophenoxy) methyl] ethylene oxide, 2H- perfluor -5,8,11,14,17- pentamethyl -3,
6,9,12,15,18- six oxa- heneicosanes, ten difluoro hexane of 2- (trifluoromethyl) -3- ethyoxyl, ten fluoro- 4- (pentafluoroethyl group)
Oxepane sulfonic acid potassium salt, 1,1,1,2,2,3,4,5,5,6,6,6- ten two fluoro- 3,4- bis- (trifluoromethyl) hexane, perfluor 20
Alkane, 1H, 6H- perflexane, 1,7- difluoro heptane, 1,1,1,2,2,3,3,4,5,5,6,6,6- ten trifluorohexane, 1,1,2,2,
5,5,6,6- pungent fluorine hexanes, perfluor to terpane, heptafluoro-propane, PF 5070, perfluor (methyl decahydronaphthalenes), perfluoropolyether,
Perfluor -1- butane sulfonic acid, perflenapent, perfluor (hexahydrotoluene), perfluor (2,2,3,3- 4-methyl-butane), perfluor -1- are pungent
Alkane, perflexane, N- perfluor n-decane, perfluoro -1,2- dimethyl cyclohexane, perfluor pentadecane, Perfluorononane, the positive fourth of perfluor
Alkane, perfluor dodecane, the perfluor tetradecane, perfluor -2,7- dimethyl octane, perfluor hexadecane, perfluor -2,3,5,6- tetramethyl-rings
Hexane, perfluor tridecane, trifluoromethyl-cyclopentane, perfluoro-2-methyl cyclobutane, (perfluoro hexyl) benzene, perfluor-(1,3,5- front three
Base benzene), it is perfluorobutyl ethane, perfluorobutyl ether, perfluorotetracosane, perfluoro hexyl ethane, perfluor tetraethyleneglycol dimethyl ether, complete
Fluoro- 2- methybutane, perfluor are to terpane, perfluorooctyl ethane, 3- (perfluoro hexyl) propylene oxide, 3- (perfluoro hexyl) epoxy
Propane, 3- (2- perfluoro hexyl ethyoxyl) -1,2- propylene oxide, 3- (Sonazoid) -1,2- propylene oxide, (perfluor is just by 3-
Octane) -1,2- propylene oxide, 1H, the 1H- perfluor -1- tetradecane, 2H- perfluor 15- methyl -3,6- dioxanonane, 3- (perfluor -
5- methylhexyl) -1,2- propylene oxide, 1H- perflenapent, 1- (perfluor-n- hexyl) dodecane, 1- (perfluor-n- octyl) ten
Four alkane, 1H, 6H- perflexane, 1- (perfluor-n- hexyl) decane, 1H- perfluor -2,4,4,-trimethylpentane, 1H, 10H- perfluor
Decane, 1H- perfluor -2,6- dimethyl heptane, 1- methyl -4- (perfluoro-ethyl) toluene, 2H- perfluor (2- methylpentane), ethyl
Perfluorobutyl ether, 8- perfluoro decyl octane, perfluor iso-butane, perfluorobutyl methyl ethers, perfluoro propene oxid, 2- trifluoromethyl are complete
At least one of amyl fluoride and 2H-3H- perflenapent.
6. coating composition as described in claim 1, which is characterized in that the structural formula of the polysilazane are as follows:
Wherein, R1For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy, alkyl siloxy or alkanamine
Base, R2For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy, alkyl siloxy or alkylamino radical, R3For hydrogen-based, alkane,
Cycloalkane, olefine, aryl, alkoxy, alkyl siloxy or alkylamino radical.
7. coating composition as claimed in claim 6, which is characterized in that the R1And R2At least one of be hydrogen-based or chain
Alkene.
8. coating composition as described in claim 1, which is characterized in that the molecular weight of the polysilazane is 100~1000.
9. coating composition as described in claim 1, which is characterized in that the structural formula of the polysiloxanes are as follows:
Wherein, R4For hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy or alkyl siloxy, R5For
Hydrogen-based, alkane, cycloalkane, olefine, aryl, alkoxy or alkyl siloxy.
10. coating composition as described in claim 1, which is characterized in that the molecular weight of the polysiloxanes be 100~
1300。
11. such as the described in any item coating compositions of claim 2-10, which is characterized in that the preparation of the coating composition is former
Material further includes solvent, and the range that the solvent accounts for the mass percent of the coating composition is 10~66%, the solvent choosing
From at least one of alkane solvents, ether solvent, ketones solvent and benzenesulfonamide derivative species solvent.
12. coating composition as claimed in claim 11, which is characterized in that the alkane solvents are selected from n-hexane, just pungent
At least one of alkane, n-decane, chloroform, methylene chloride, dichloroethylene and mineral oil are a variety of;The ether solvent
Selected from least one of ether, petroleum ether and butyl oxide;The ketones solvent is selected from acetone, methyl ethyl ketone, cyclohexanone and different
At least one of phorone;The benzenesulfonamide derivative species solvent is selected from toluene, meta-xylene, paraxylene, ortho-xylene and chlorine
At least one of benzene.
13. such as the described in any item coating compositions of claim 2-10, which is characterized in that the preparation of the coating composition is former
Material further includes catalyst, and the range that the catalyst accounts for the mass percent for preparing raw material is 0.01~5%, the catalysis
Agent is amines catalyst and/or metal-based catalysts.
14. coating composition as claimed in claim 13, which is characterized in that the amines catalyst is selected from fatty amine, alicyclic ring
One of race's amine, hydramine and aromatic amine are a variety of, and the fatty amine is in diethylamine, triethylamine and triethylene tetramine
It is at least one;The cycloaliphatic amines are selected from least one of triethylenediamine, piperazine, piperidines and morpholine;The hydramine choosing
From N, N- dimethylethanolamine, diisopropanolamine (DIPA) and N, at least one of N- diethyl ethylene diamine;The aromatic amine is selected from benzene
At least one of amine, o-phenylenediamine, benzidine and n,N-Dimethylaniline.
15. coating composition as claimed in claim 13, which is characterized in that the metal-based catalysts are organotin catalysts
And/or palladium class catalyst, the organotin catalysts are selected from dibutyltindilaurylmercaptide cinnamic acid rouge, stannous octoate, stannous methide and three
At least one of phenyltin;The palladium class catalyst is selected from carbon/palladium, palladium chloride, propionic acid palladium salt, acetic acid palladium salt and triphenyl
At least one of phosphorus palladium.
16. such as the described in any item coating compositions of claim 2-10, which is characterized in that the preparation of the coating composition is former
Material further includes filler, and the range that the filler accounts for the mass percent for preparing raw material is 1~50%, and the filler is selected from carbon
SiClx, aluminium oxide, titanium oxide, zinc oxide, magnesia, aluminium hydroxide, white carbon black, concave convex rod, kaolin, bentonite, glass are micro-
At least one of ball and ceramic microsphere.
17. coating composition as claimed in claim 11, which is characterized in that the raw material for preparing of the coating composition further includes
Catalyst and filler, the range that the catalyst accounts for the mass percent of the coating composition is 0.01~5%, the filler
The range for accounting for the mass percent of the coating composition is 1~50%, and the polysiloxanes and polysilazane account for the coating
The range of the mass percent of composition is 10%~60%, and the anti-fouling agent of the fluorine richness accounts for the quality hundred for preparing raw material
The range for dividing ratio is 0.01~15%.
18. a kind of preparation method of coating composition, comprising the following steps:
Offer prepares raw material, described to prepare the anti-fouling agent and colorant that raw material includes polysilazane, polysiloxanes, fluorine richness;
Mixing polysilazane and polysiloxanes, polysilazane and polysiloxanes are copolymerized, and generate the poly- silicon oxygen of polysilazane-
Alkyl copolymer;
The anti-fouling agent and colorant of fluorine richness are added into the polysilazane-polysiloxane copolymer, the Coating material composition is made
Object.
19. the preparation method of coating composition as claimed in claim 18, which is characterized in that mixing polysilazane and poly- silicon oxygen
After alkane, the preparation method of the coating composition further include: the step of catalyst is added into polysilazane and polysiloxanes,
In, the range that the catalyst accounts for the mass percent for preparing raw material is 0.01~5%, and the catalyst is amines catalysis
Agent and/or metal-based catalysts.
20. the preparation method of coating composition as claimed in claim 18, which is characterized in that generate the poly- silicon oxygen of polysilazane-
After alkyl copolymer, before obtaining the coating composition, the preparation method of the coating composition further include: poly- to polysilazane-
The step of solvent is added in silicone copolymers, wherein the range that the solvent accounts for the mass percent for preparing raw material is
10~66%, the solvent in alkane solvents, ether solvent, ketones solvent and benzenesulfonamide derivative species solvent at least one
Kind.
21. the preparation method of coating composition as claimed in claim 18, which is characterized in that generate the poly- silicon oxygen of polysilazane-
After alkyl copolymer, before obtaining the coating composition, the preparation method of the coating composition further include: poly- to polysilazane-
The step of filler is added in silicone copolymers, wherein the range that the filler accounts for the mass percent for preparing raw material is 1
~50%, the filler be selected from silicon carbide, aluminium oxide, titanium oxide, zinc oxide, magnesia, aluminium hydroxide, white carbon black, concave convex rod,
At least one of kaolin, bentonite, glass microsphere and ceramic microsphere.
22. a kind of coating piece, which is characterized in that the coating piece includes matrix and the coating for being formed in matrix surface, the painting
Contain the coating composition as described in any one of claim 1-17 in layer.
23. coating piece as claimed in claim 22, which is characterized in that the range of the thickness of the coating is 1~100 micron.
24. a kind of preparation method of coating piece, comprising the following steps:
Matrix and the coating composition as described in any one of claim 1-17 are provided;
By the coating composition in the surface of matrix, the coating piece is made.
25. a kind of household electrical appliance, which is characterized in that the household electrical appliance include such as the described in any item paintings of claim 22-23
Cover part.
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CN201811175205.8A CN109321133B (en) | 2018-10-08 | 2018-10-08 | Coating composition and preparation method thereof, coated piece and preparation method thereof, and household appliance |
PCT/CN2019/109986 WO2020073894A1 (en) | 2018-10-08 | 2019-10-08 | Coating composition and preparation method therefor, coating member and preparation method therefor, and home appliance |
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CN201811175205.8A CN109321133B (en) | 2018-10-08 | 2018-10-08 | Coating composition and preparation method thereof, coated piece and preparation method thereof, and household appliance |
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Cited By (4)
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WO2020073889A1 (en) * | 2018-10-08 | 2020-04-16 | 广东美的厨房电器制造有限公司 | Coating composition and preparation method therefor, coating member and preparation method therefor, and household appliance |
WO2020073894A1 (en) * | 2018-10-08 | 2020-04-16 | 广东美的厨房电器制造有限公司 | Coating composition and preparation method therefor, coating member and preparation method therefor, and home appliance |
CN113174198A (en) * | 2021-05-21 | 2021-07-27 | 佛山市顺德区美的洗涤电器制造有限公司 | High-temperature-resistant coating composition, high-temperature-resistant coating, preparation method and application of high-temperature-resistant coating, and high-temperature-resistant coating |
CN113402974A (en) * | 2021-06-02 | 2021-09-17 | 佛山市顺德区美的洗涤电器制造有限公司 | Coating composition, coating, preparation method and application thereof, and coating |
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WO2020073889A1 (en) * | 2018-10-08 | 2020-04-16 | 广东美的厨房电器制造有限公司 | Coating composition and preparation method therefor, coating member and preparation method therefor, and household appliance |
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CN113174198B (en) * | 2021-05-21 | 2022-04-08 | 佛山市顺德区美的洗涤电器制造有限公司 | High-temperature-resistant coating composition, high-temperature-resistant coating, preparation method and application of high-temperature-resistant coating, and high-temperature-resistant coating |
CN113402974A (en) * | 2021-06-02 | 2021-09-17 | 佛山市顺德区美的洗涤电器制造有限公司 | Coating composition, coating, preparation method and application thereof, and coating |
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