CN112574390A - High-wear-resistance UV resin with anti-fingerprint function and preparation method thereof - Google Patents
High-wear-resistance UV resin with anti-fingerprint function and preparation method thereof Download PDFInfo
- Publication number
- CN112574390A CN112574390A CN202110222736.3A CN202110222736A CN112574390A CN 112574390 A CN112574390 A CN 112574390A CN 202110222736 A CN202110222736 A CN 202110222736A CN 112574390 A CN112574390 A CN 112574390A
- Authority
- CN
- China
- Prior art keywords
- reaction
- resin
- hydroxyl
- isocyanate
- polyurethane
- 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
- 239000011347 resin Substances 0.000 title claims abstract description 48
- 229920005989 resin Polymers 0.000 title claims abstract description 48
- 230000003666 anti-fingerprint Effects 0.000 title claims abstract description 15
- 238000002360 preparation method Methods 0.000 title abstract description 6
- 238000006243 chemical reaction Methods 0.000 claims abstract description 80
- -1 polysiloxane Polymers 0.000 claims abstract description 68
- 239000004814 polyurethane Substances 0.000 claims abstract description 35
- 229920002635 polyurethane Polymers 0.000 claims abstract description 35
- 239000012948 isocyanate Substances 0.000 claims abstract description 28
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 27
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 26
- 150000002009 diols Chemical class 0.000 claims abstract description 24
- 239000007809 chemical reaction catalyst Substances 0.000 claims abstract description 23
- 229920000728 polyester Polymers 0.000 claims abstract description 17
- 239000010702 perfluoropolyether Substances 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 11
- 239000011737 fluorine Substances 0.000 claims abstract description 11
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 11
- 239000010703 silicon Substances 0.000 claims abstract description 11
- AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical compound OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 claims abstract description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 7
- 239000002994 raw material Substances 0.000 claims abstract description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 40
- 239000013067 intermediate product Substances 0.000 claims description 34
- 238000003756 stirring Methods 0.000 claims description 31
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 28
- 239000007787 solid Substances 0.000 claims description 27
- 238000005299 abrasion Methods 0.000 claims description 21
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- 238000004321 preservation Methods 0.000 claims description 17
- 238000010438 heat treatment Methods 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 13
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 11
- 238000007865 diluting Methods 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 10
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 9
- 239000000047 product Substances 0.000 claims description 8
- 239000013638 trimer Substances 0.000 claims description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 229920005862 polyol Polymers 0.000 claims description 6
- PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 4
- OBOXTJCIIVUZEN-UHFFFAOYSA-N [C].[O] Chemical group [C].[O] OBOXTJCIIVUZEN-UHFFFAOYSA-N 0.000 claims description 4
- 125000002723 alicyclic group Chemical group 0.000 claims description 4
- 229920003232 aliphatic polyester Polymers 0.000 claims description 4
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 4
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 3
- 125000000524 functional group Chemical group 0.000 claims description 3
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 3
- 229920000515 polycarbonate Polymers 0.000 claims description 3
- 239000004417 polycarbonate Substances 0.000 claims description 3
- 230000035484 reaction time Effects 0.000 claims description 3
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 claims description 2
- PTPIRFSXRFIROJ-UHFFFAOYSA-N 2-(3-hydroxyphenoxy)ethane-1,1-diol Chemical compound OC(O)COC1=CC=CC(O)=C1 PTPIRFSXRFIROJ-UHFFFAOYSA-N 0.000 claims description 2
- CTNICFBTUIFPOE-UHFFFAOYSA-N 2-(4-hydroxyphenoxy)ethane-1,1-diol Chemical compound OC(O)COC1=CC=C(O)C=C1 CTNICFBTUIFPOE-UHFFFAOYSA-N 0.000 claims description 2
- FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical compound OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 claims description 2
- IBFJDBNISOJRCW-UHFFFAOYSA-N 3-methylphthalic acid Chemical compound CC1=CC=CC(C(O)=O)=C1C(O)=O IBFJDBNISOJRCW-UHFFFAOYSA-N 0.000 claims description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 2
- TWWAWPHAOPTQEU-UHFFFAOYSA-N 4-methyl-2-benzofuran-1,3-dione Chemical compound CC1=CC=CC2=C1C(=O)OC2=O TWWAWPHAOPTQEU-UHFFFAOYSA-N 0.000 claims description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
- GTTSNKDQDACYLV-UHFFFAOYSA-N Trihydroxybutane Chemical compound CCCC(O)(O)O GTTSNKDQDACYLV-UHFFFAOYSA-N 0.000 claims description 2
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 claims description 2
- 238000007259 addition reaction Methods 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 230000001588 bifunctional effect Effects 0.000 claims description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 claims description 2
- VEIOBOXBGYWJIT-UHFFFAOYSA-N cyclohexane;methanol Chemical compound OC.OC.C1CCCCC1 VEIOBOXBGYWJIT-UHFFFAOYSA-N 0.000 claims description 2
- GTZOYNFRVVHLDZ-UHFFFAOYSA-N dodecane-1,1-diol Chemical compound CCCCCCCCCCCC(O)O GTZOYNFRVVHLDZ-UHFFFAOYSA-N 0.000 claims description 2
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 claims description 2
- OTLDLKLSNZMTTA-UHFFFAOYSA-N octahydro-1h-4,7-methanoindene-1,5-diyldimethanol Chemical compound C1C2C3C(CO)CCC3C1C(CO)C2 OTLDLKLSNZMTTA-UHFFFAOYSA-N 0.000 claims description 2
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920001451 polypropylene glycol Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 230000002195 synergetic effect Effects 0.000 abstract description 2
- 239000003973 paint Substances 0.000 description 29
- 239000000243 solution Substances 0.000 description 22
- 238000000576 coating method Methods 0.000 description 19
- 239000011248 coating agent Substances 0.000 description 14
- 238000012360 testing method Methods 0.000 description 13
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 210000002268 wool Anatomy 0.000 description 6
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 239000012975 dibutyltin dilaurate Substances 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 3
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 3
- 230000003373 anti-fouling effect Effects 0.000 description 3
- VPASWAQPISSKJP-UHFFFAOYSA-N ethyl prop-2-enoate;isocyanic acid Chemical compound N=C=O.CCOC(=O)C=C VPASWAQPISSKJP-UHFFFAOYSA-N 0.000 description 3
- 238000011056 performance test Methods 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001723 curing Methods 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- IIQWTZQWBGDRQG-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate;isocyanic acid Chemical compound N=C=O.CCOC(=O)C(C)=C IIQWTZQWBGDRQG-UHFFFAOYSA-N 0.000 description 2
- WELLGRANCAVMDP-UHFFFAOYSA-N isocyanatoethane;prop-2-enoic acid Chemical group CCN=C=O.OC(=O)C=C WELLGRANCAVMDP-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000000016 photochemical curing Methods 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000013538 functional additive Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000013035 low temperature curing Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 229920000921 polyethylene adipate Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5003—Polyethers having heteroatoms other than oxygen having halogens
- C08G18/5015—Polyethers having heteroatoms other than oxygen having halogens having fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/61—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/675—Low-molecular-weight compounds
- C08G18/677—Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups
- C08G18/678—Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
- C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
- C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
- C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
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- 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
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- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1656—Antifouling paints; Underwater paints characterised by the film-forming substance
- C09D5/1662—Synthetic film-forming substance
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Abstract
The invention relates to a high-wear-resistance UV resin with an anti-fingerprint function and a preparation method thereof, wherein the resin comprises the following raw materials: isocyanate mixture, perfluoropolyether alcohol with hydroxyl at one end, mixture of single-end hydroxyl polysiloxane and double-end hydroxyl polysiloxane, linear polyester diol without fluorine and silicon, hydroxyl acrylate containing a polyurethane structure and a polyurethane reaction catalyst; according to the invention, through the reaction among the components, the perfluoropolyether and the organosilicon chain segment are simultaneously introduced into the polymer molecular chain of the UV resin, and the friction coefficient and the surface energy of the resin surface are reduced by utilizing the synergistic effect of the fluorine and silicon molecules, so that the prepared UV resin has good fingerprint-resistant and wear-resistant properties; meanwhile, the high-content carbamate is introduced into the polymer molecular chain of the UV resin to improve the hydrogen bond content of the molecular chain, so that the cohesive energy of the molecular chain is improved, and the wear resistance of the UV resin is further improved.
Description
Technical Field
The invention relates to the technical field of high polymer materials, in particular to high-wear-resistance UV resin with an anti-fingerprint function, and further relates to a method for preparing the UV resin.
Background
With the rapid development of the 5G technology, the utilization rate of plastic materials in the surfaces of electronic communication equipment and the like is gradually improved, and the plastic materials have a tendency of replacing the existing glass, ceramics and metals. However, the plastic surface is not wear-resistant and is easy to be stained, and the wear-resistant and stain-resistant treatment is required in practical application.
The UV coating belongs to a purple-line curing coating, mainly comprises an oligomer, a reactive diluent, a photoinitiator, an auxiliary agent and the like, has higher hardness and good wear resistance, can improve the wear resistance when being coated on the surface of plastic, has the characteristics of low-temperature curing, energy conservation, no pollution, quick film forming, convenient construction and the like, and can effectively avoid the damage of high temperature in the production process to electronic product materials. The curing mechanism of the UV coating is mainly acrylate functional group free copolymerization reaction, a large number of polar functional groups exist on the surface of a cured paint film, although the paint film has higher hardness, the surface tension of the paint film surface is high, water and oil substances are easy to spread on the surface of the paint film, and therefore the surface of the UV coating is very weak to stain.
In recent years, researchers have proposed that an assistant with an anti-fingerprint function is added into the existing UV coating to solve the problem that the surface of a paint film is not resistant to stains, for example, a Chinese patent with application number CN200580014573.9 discloses a perfluoropolyether modified acrylate with an anti-stain effect, and the anti-stain property of the paint film can be improved by adding the perfluoropolyether modified acrylate into the UV coating, but the compound has poor compatibility with common UV resin, so that the wear resistance of the final paint film is poor.
Another US patent with US15029867 discloses an anti-fingerprint additive for UV coatings which gives the paint film a high anti-fingerprint and abrasion resistance, however, the compound can still only be used as a functional additive and cannot be used as the main UV resin in the formulation of UV coatings, so that the paint film finally shows an unsatisfactory abrasion resistance and cannot meet the requirement of high abrasion resistance.
Therefore, there is a need to provide a new technical solution to overcome the above-mentioned drawbacks.
Disclosure of Invention
The invention aims to provide a high-wear-resistance UV resin with an anti-fingerprint function and a preparation method thereof, which can effectively solve the technical problems.
In order to achieve the purpose of the invention, the following technical scheme is adopted:
a high wear-resistant UV resin with an anti-fingerprint function comprises the following raw materials: isocyanate mixture, perfluoropolyether alcohol containing hydroxyl at one end, mixture containing single-end hydroxyl polysiloxane and double-end hydroxyl polysiloxane, linear polyester diol containing no fluorine and silicon, hydroxyl acrylate containing a polyurethane structure and a polyurethane reaction catalyst.
Preferably, the sum of the number of moles of the hydroxyl functional groups in the perfluoropolyether alcohol having a hydroxyl group at one end, the mixture of the single-terminal hydroxyl polysiloxane and the double-terminal hydroxyl polysiloxane, the linear polyester diol containing no fluorine and silicon, and the hydroxy acrylic acid containing a polyurethane structure is equal to the number of moles of the isocyanate functional groups in the isocyanate mixture.
Preferably, the isocyanate mixture comprises:
an isocyanate compound having a functionality of 3 for the isocyanate group;
and an isocyanate compound having a functionality of 2 for the isocyanate group;
the sum of the number of moles of the perfluoropolyether alcohol having a hydroxyl group at one end and the number of moles of the monohydroxy polysiloxane at one end is equal to the number of moles of the isocyanate compound having a functionality of 3;
the number of moles of the isocyanate compound having a functionality of 2 in the isocyanate group is 2 times the number of moles of the double-terminal hydroxyl polysiloxane.
Preferably, the isocyanate compound having a functionality of 3 in the isocyanate group is selected from one or more of a trimer of toluene diisocyanate, a trimer of isophorone diisocyanate and a trimer of hexamethylene diisocyanate;
the isocyanate compound with the isocyanate group functionality of 2 is selected from one or more of 2, 4-toluene diisocyanate, 2, 6-toluene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, dicyclohexylmethane diisocyanate, 1, 5-naphthalene diisocyanate and diphenylmethane diisocyanate.
Preferably, the perfluoropolyether alcohol having a hydroxyl group at one end has a structure represented by the following formula (1) or formula (2) or formula (3) or formula (4) or formula (5) or formula (6):
CF3CF2CF2O(CF(CF3)CF2O)nCF(CF3)CH2OH （1）；
CF3CF2CF2O(CF(CF3)CF2O)nCF(CF3)CH2O(CH2CH2O)mH （2）;
CF3CF2CF2O(CF2CF2CF2O)nCF2CF2CH2OH （3）；
CF3CF2CF2O(CF2CF2CF2O)nCF2CF2CH2O(CH2CHO)mH （4）；
CF3CF2CF2O(CF(CF3)CF2O)nCF(CF3)CO-X1-OH （5）；
CF3CF2CF2O(CF2CF2CF2O)nCF2CF2CO-X1-OH （6）；
n in the formulas (1) to (6) is a natural number and satisfies 2. ltoreq. n.ltoreq.60; m is a natural number and satisfies that m is more than or equal to 1 and less than or equal to 10; x1Has the structural formula of-O-R1-OH or-NH-R-OH, R1Is a divalent alkyl group containing a saturated carbon-oxygen chain.
Preferably, in the mixture containing single-terminal carbon hydroxyl polysiloxane and double-terminal carbon hydroxyl polysiloxane:
the chemical formula of the single-end carbon hydroxyl polysiloxane is shown as the following formula (7):
a dicarbohydroxyl polysiloxane having the formula (8):
wherein,
in the above formulas (7) and (8):
R2and R3Is also a monovalent alkyl radical containing a saturated carbon-oxygen chain and having the formula CqH2q-1Wherein q is a natural number and satisfies 1. ltoreq. q.ltoreq.10;
X2has a structural formula of CH2(CH2)cCH2OCH2(CH2)dCH2；
a is a natural number and satisfies a condition that a is more than or equal to 2 and less than or equal to 100;
b is a natural number and satisfies that b is more than or equal to 2 and less than or equal to 100;
c is an integer and satisfies 0-10;
d is an integer and satisfies 0. ltoreq. d.ltoreq.10.
Preferably, the linear polyester diol containing no fluorine and silicon is selected from one or more of aliphatic polyester diol, alicyclic polyester diol and aromatic polyester diol.
Preferably, the aliphatic polyester diol is selected from one or more of polyethylene adipate diol, polycarbonate diol and polypropylene adipate diol;
the synthetic raw materials corresponding to the aliphatic ring in the alicyclic polyester diol structural unit are selected from one or more of cyclohexane dimethanol, cyclohexanediol, tricyclodecanedimethanol, dodecanediol and spiroglycol;
the synthetic raw materials corresponding to the aromatic ring in the aromatic polyester diol structural unit are selected from one or more of the combination of poly phthalic anhydride, methyl phthalic anhydride, phthalic acid, methyl phthalic acid, hydroquinone bis hydroxyethyl ether and resorcinol bis hydroxyethyl ether.
Preferably, the functionality of the hydroxy acrylate containing a polyurethane structure is at least 5.
Preferably, the hydroxyl acrylate containing a polyurethane structure is an equimolar ratio addition reaction product of a small molecular polyol compound and an acrylate compound containing an isocyanate group.
Preferably, the small molecule polyol compound is selected from one or more of glycerol, butanetriol, hexanetriol, dipentaerythritol and tripentaerythritol.
Preferably, the functionality of the isocyanate group in the acrylate compound containing an isocyanate group is 1.
Preferably, the acrylate compound having an isocyanate group is selected from the group consisting of an equimolar adduct of isophorone diisocyanate and hydroxyethyl acrylate, an equimolar adduct of isophorone diisocyanate and hydroxyethyl methacrylate, an equimolar adduct of 2, 4-toluene diisocyanate and hydroxyethyl acrylate, an equimolar adduct of 2, 4-toluene diisocyanate and hydroxyethyl methacrylate, an equimolar adduct of isophorone diisocyanate and pentaerythritol triacrylate, a combination of one or more of equimolar adducts of 2, 4-toluene diisocyanate and pentaerythritol triacrylate, equimolar adducts of isophorone diisocyanate and dipentaerythritol pentaacrylate, equimolar adducts of 2, 4-toluene diisocyanate and dipentaerythritol pentaacrylate, isocyanate ethyl acrylate, and isocyanate ethyl methacrylate.
The invention also provides a method for preparing the high-wear-resistance UV resin with the fingerprint resistance function, which comprises the following process steps:
step 1: diluting an isocyanate compound with isocyanate group functionality of 3 and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding perfluoropolyether alcohol with one end containing hydroxyl under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to obtain a solution containing an intermediate product 1, wherein the solid content of a reaction system is 10-70%;
step 2: diluting an isocyanate compound with isocyanate group functionality of 3 and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding single-end carbon hydroxyl polysiloxane under the stirring condition, and carrying out heat preservation reaction after the dripping is finished to prepare a solution containing an intermediate product 2, wherein the solid content of a reaction system is 10-70%;
and step 3: diluting an isocyanate compound with isocyanate group functionality of 2 and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dripping double-ended carbon hydroxyl polysiloxane under the condition of stirring, and carrying out heat preservation reaction after dripping is finished to prepare a solution containing an intermediate product 3, wherein the solid content of a reaction system is 10-70%;
and 4, step 4: uniformly mixing a solution containing an intermediate product 1, an intermediate product 2 and an intermediate product 3, heating under the protection of dry nitrogen, slowly dropwise adding linear polyester dihydric alcohol which does not contain fluorine and silicon under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to prepare a solution containing an intermediate product 4, wherein the solid content of a reaction system is 10-70%;
and 5: diluting a bifunctional isocyanate compound and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding a monohydroxy acrylate compound under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to obtain a solution containing an intermediate product 5, wherein the solid content of a reaction system is 10-70%;
step 6: diluting a small molecular polyol compound and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding hydroxyl acrylate containing a polyurethane structure under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to obtain a solution containing an intermediate product 6, wherein the solid content of a reaction system is 10-70%;
and 7: under the conditions of dry nitrogen protection and stirring, heating the solution containing the intermediate product 4, then slowly dropwise adding the solution containing the intermediate product 6 into the solution containing the intermediate product 4, and carrying out heat preservation reaction after the dropwise adding is finished to obtain the solution containing the UV resin product, wherein the solid content of the product is 10-70%.
Preferably, the stirring speed during material dropping in the reaction systems of the step 1, the step 2, the step 3 and the step 4 is 100-;
the stirring speed during material dropping in the reaction systems of the step 5, the step 6 and the step 7 is 100-500 rpm, the material dropping time is 1-5 h, the temperature during the heat preservation reaction is 10-80 ℃, and the reaction time is 1-5 h.
Preferably, the molar ratio of the isocyanate group to the hydroxyl group in the reaction systems of the step 1 and the step 2 is 3: 1;
the molar ratio of the isocyanate group to the hydroxyl group in the reaction systems of the step 3 and the step 5 is 2: 1.
Preferably, the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 1 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 2 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 3 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 5 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 6 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system.
Preferably, the difunctional isocyanate compound in the step 5 is selected from one or more of isophorone diisocyanate and 2, 4-toluene diisocyanate; the acrylate compound containing monohydroxy in the step 5 is one or more of hydroxyethyl acrylate, hydroxyethyl methacrylate, pentaerythritol triacrylate and dipentaerythritol pentaacrylate.
Preferably, the hydroxyl acrylate containing a polyurethane structure in the step 6 is selected from one or more of the group consisting of intermediate 5, isocyanate ethyl acrylate and isocyanate ethyl methacrylate.
Compared with the prior art, the invention has the following beneficial effects:
1. according to the invention, through the reaction among the components, the perfluoropolyether and the organosilicon chain segment are simultaneously introduced into the polymer molecular chain of the UV resin, and the friction coefficient and the surface energy of the resin surface are reduced by utilizing the synergistic effect of the fluorine and silicon molecules, so that the prepared UV resin has good fingerprint-resistant and wear-resistant properties; meanwhile, the high-content carbamate is introduced into the polymer molecular chain of the UV resin to improve the hydrogen bond content of the molecular chain, so that the cohesive energy of the molecular chain is improved, and the wear resistance of the UV resin is further improved.
2. The UV resin prepared by the invention has excellent intermiscibility with common UV resin, and can be used as main resin to be compounded with the common UV resin to prepare the UV coating with fingerprint resistance and high wear resistance; meanwhile, performance tests are carried out on the UV coating prepared from the UV resin disclosed by the invention, and the results show that the final paint film not only has very high fingerprint and wear resistance, but also the surface of the paint film still keeps a high water contact angle after the paint film is worn by steel wool, namely the surface of the paint film still has very high anti-fouling property after the paint film is worn by the steel wool.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the following will clearly and completely describe the technical solutions in the embodiments of the present invention, and it is obvious that the described embodiments are some embodiments of the present invention, but not all embodiments.
Firstly, resin preparation
Example 1
This example provides a high abrasion resistant UV resin 1# sample (UV-1) with anti-fingerprint function, which is prepared as follows:
(1) after 7.25 g of a trimer of isophorone diisocyanate (trade name T1890/100, supplied by winning company) and 0.15 g of dibutyltin dilaurate were diluted with 47.25 g of benzotrifluoride, the temperature was raised to 80 ℃ under the protection of dry nitrogen, and 40.00g of perfluoropolyether alcohol (trade name DOL-4000, molecular formula CF-4000, slowly added dropwise with stirring3CF2CF2O(CF(CF3)CF2O)nCF(CF3)CH2OH, the molecular weight is 4000, which is provided by Taicang chemical environmental protection chemical company), the stirring speed is 200 r/min, the dripping time is 1h, the reaction temperature is kept after the dripping is finished, and the reaction is continued for 2h to prepare a solution containing an intermediate product 1;
(2) after 7.25 g of trimer of isophorone diisocyanate (the trademark is T1890/100, provided by winning company) and 0.15 g of dibutyltin dilaurate are diluted by 17.25 g of benzotrifluoride, the temperature is raised to 80 ℃ under the protection of dry nitrogen, 10.00g of single-end hydroxy dimethyl silicone oil (the trademark is IOTA2050, the molecular weight is 1000, provided by Anhui Eyota Silicone oil Co., Ltd.) is slowly dripped under the stirring condition, the stirring speed is 200 r/min, the dripping time is 1h, the reaction temperature is kept after the dripping is finished, and the reaction is continued for 2h, so that a solution containing an intermediate product 2 is prepared;
(3) after 17.80 g of isophorone diisocyanate and 0.15 g of dibutyltin dilaurate are diluted by 47.80 g of benzotrifluoride, the temperature is raised to 80 ℃ under the protection of dry nitrogen, 40.00g of double-end hydroxyl dimethyl silicone oil (the trade name is Silok, the molecular weight is 1000, provided by Stocko high molecular polymer Co., Ltd., Guangzhou) is slowly dripped under the stirring condition, the stirring speed is 200 r/min, the dripping time is 1h, the dripping is finished, the reaction temperature is kept, and the reaction is continued for 2h, so that a solution containing an intermediate product 3 is prepared;
(4) uniformly mixing the solution containing the intermediate product 1, the intermediate product 2 and the intermediate product 3, heating to 50 ℃ under the protection of dry nitrogen, slowly dropwise adding a mixed solution of 160.00 g of polycarbonate diol (the brand is UH-CARB200, the molecular weight is 2000 and the molecular weight is provided by Japan and Japan) and 160.00 g of butanone under the stirring condition, stirring at the speed of 200 r/min for 1h, and keeping the reaction temperature and continuing to react for 2h after the dropwise adding is finished to obtain a solution containing an intermediate product 4;
(5) after 23.71 g of tripentaerythritol, 0.40 g of p-hydroxyanisole and 0.15 g of dibutyltin dilaurate are diluted by 55.00 g of butanone, the temperature is raised to 50 ℃ under the protection of dry nitrogen, 31.29g of isocyanate ethyl acrylate is slowly dripped under the stirring condition, the stirring speed is 200 r/min, the dripping time is 1h, the reaction temperature is kept after the dripping is finished, and the reaction is continued for 2h, so that a solution containing an intermediate product 6 is prepared;
(6) under the protection of dry nitrogen and stirring, heating the solution containing the intermediate product 4 to 50 ℃, slowly dropwise adding the solution containing the intermediate product 6, stirring at the speed of 200 revolutions per minute for 4 hours, keeping the reaction temperature after dropwise adding is finished, and continuously reacting for 4 hours to obtain the product UV-1 with the solid content of 50%.
Example 2
This example provides a high abrasion resistant UV resin 1# sample (UV-2) with anti-fingerprint function, which is prepared as follows:
following the procedure and procedure as shown in example 1, the tripentaerythritol was replaced by dipentaerythritol in step (5), the corresponding mass was replaced by 16.24g, the mass of ethyl isocyanate acrylate was replaced by 22.46g, and the mass of butanone in this step was replaced by 38.70g, all other conditions and masses being the same as in example 1, to give UV-2, a solid content of 50%.
Example 3
This example provides a high abrasion resistant UV resin 1# sample (UV-3) with anti-fingerprint function, which is prepared as follows:
according to the procedure and process shown in example 1, the mass of isophorone diisocyanate was changed to 8.90g, the mass of dihydroxy dimethylsilicone oil was changed to 20.00g, and the mass of trifluorotoluene in this step was changed to 28.90g in step (3); in step (5), tripentaerythritol is replaced by dipentaerythritol, the corresponding mass is replaced by 16.24g, the mass of ethyl isocyanate acrylate is replaced by 22.46g, and the mass of butanone in this step is replaced by 38.70 g; the remaining conditions and mass were the same as in example 1, giving the product UV-3, a solids content of 50%.
Preparation of coatings and paint films
Step 1: compounding UV coating according to a formula (the addition amount of each component is calculated by weight parts) shown in Table 1, and uniformly stirring and mixing at a high speed;
step 2: carrying out reaction and secondary filtration on the UV coating by using a PP (polypropylene) filter element with the diameter of 2 microns;
and step 3: scraping the filtered coating on an acrylic plastic plate by using a 20-micron wire rod, and baking for 5 minutes in a 55-DEG C blast drying oven;
and 4, step 4: placing the baked plastic plate on a crawler-type UV photocuring machine for photocuring operation, wherein a light source is a high-pressure mercury lamp, the wavelength is 365nm, and finally preparing the cured acrylic plate coated with the UV coating;
table 1 coating formulation table
In table 1, CN9013NS represents a multifunctional urethane acrylate produced by Sartomer corporation, which has a functionality of 9; SIO-P100 represents the nano-silica powder produced by Shanghai Zhengnano materials. KY1203 represents an anti-fingerprint functional auxiliary agent for UV coating produced by Japan shinier-shin-Etsu, and contains an acrylate functional group which can be cured by UV light.
Table 2 paint film performance test tables for paints 1 to 6
The paint film property test methods for paints 1 to 6 in table 2 are as follows:
1) hardness: the pencil hardness test method is adopted:
the test was carried out according to the method of GBT 6739-.
2) The adhesion test method comprises the following steps:
the test was performed according to GB _ T9286-1998 method.
3) Water contact angle test method:
test pieces prepared from coatings 1 to 6 were placed on a contact angle meter (model: DSA30, supplied by kluyvers ltd, germany) with deionized water and dodecane as test media and a test droplet volume of 4 μ L, and the contact angle values of 3 droplets were recorded and the arithmetic mean of the 3 test data was taken.
4) And (3) wear resistance test:
the test pieces prepared from the coatings 1 to 6 were fixed to an abrasion resistance tester (ESIDA-NM-002, available from Shimada instruments Co., Ltd., Shenzhen), and the contact area was 2X 2cm2Binding 0000# steel wool on the contact friction probe;
applying 1000g of test load above the probe, testing for 35-40 times/min at a speed of 3-4cm in stroke, performing reciprocating friction for 3000 times, and stopping the test after performing a wear test for 20 minutes;
observing the appearance of a paint film in the abrasion area, judging the paint film to be OK if the abrasion area is not scratched, and otherwise, judging the paint film to be Fail; the water contact angle of the paint film in the abraded area was also tested.
By comparing the performance test data of the paint film of the test piece prepared by the paint 1-6, the UV paint prepared by the UV resin has a higher water contact angle and higher steel wool resistance compared with the common UV paint; meanwhile, the surface of the paint film still keeps a higher water contact angle after being worn by steel wool, namely the surface of the paint film still has high anti-fouling property after being worn by the steel wool, so that the UV resin can enhance the anti-fouling and wear-resisting properties of the UV coating and can meet the production requirements of high-wear-resisting and stain-resisting products.
Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention.
Claims (16)
1. The utility model provides a high wear-resisting UV resin with anti fingerprint function which characterized in that: the raw materials of the resin comprise the following components: isocyanate mixture, perfluoropolyether alcohol containing hydroxyl at one end, mixture containing single-end hydroxyl polysiloxane and double-end hydroxyl polysiloxane, linear polyester diol containing no fluorine and silicon, hydroxyl acrylate containing a polyurethane structure and a polyurethane reaction catalyst.
2. The high abrasion resistant UV resin with fingerprint resistance function according to claim 1, wherein: the sum of the mole numbers of the functional groups of the hydroxyl in the perfluoropolyether alcohol containing hydroxyl at one end, the mixture containing single-end carbon hydroxyl polysiloxane and double-end carbon hydroxyl polysiloxane, the linear polyester diol containing no fluorine and silicon and the hydroxyl acrylic acid containing a polyurethane structure is equal to the mole number of the functional groups of the isocyanate group in the isocyanate mixture.
3. The high abrasion resistant UV resin with fingerprint resistance function according to claim 1, wherein: the isocyanate mixture comprises:
an isocyanate compound having a functionality of 3 for the isocyanate group;
and an isocyanate compound having a functionality of 2 for the isocyanate group;
the sum of the number of moles of the perfluoropolyether alcohol having a hydroxyl group at one end and the number of moles of the monohydroxy polysiloxane at one end is equal to the number of moles of the isocyanate compound having a functionality of 3;
the number of moles of the isocyanate compound having a functionality of 2 in the isocyanate group is 2 times the number of moles of the double-terminal hydroxyl polysiloxane.
4. The high abrasion resistant UV resin with fingerprint resistance function according to claim 3, wherein:
the isocyanate compound with the isocyanate group having the functionality of 3 is selected from one or more of a trimer of toluene diisocyanate, a trimer of isophorone diisocyanate and a trimer of hexamethylene diisocyanate;
the isocyanate compound with the isocyanate group functionality of 2 is selected from one or more of 2, 4-toluene diisocyanate, 2, 6-toluene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, dicyclohexylmethane diisocyanate, 1, 5-naphthalene diisocyanate and diphenylmethane diisocyanate.
5. The high abrasion resistant UV resin with fingerprint resistance function according to claim 1, wherein: the perfluoropolyether alcohol having a hydroxyl group at one end has a structure represented by the following formula (1), formula (2), formula (3), formula (4), formula (5) or formula (6):
CF3CF2CF2O(CF(CF3)CF2O)nCF(CF3)CH2OH （1）；
CF3CF2CF2O(CF(CF3)CF2O)nCF(CF3)CH2O(CH2CH2O)mH （2）;
CF3CF2CF2O(CF2CF2CF2O)nCF2CF2CH2OH （3）；
CF3CF2CF2O(CF2CF2CF2O)nCF2CF2CH2O(CH2CHO)mH （4）；
CF3CF2CF2O(CF(CF3)CF2O)nCF(CF3)CO-X1-OH （5）；
CF3CF2CF2O(CF2CF2CF2O)nCF2CF2CO-X1-OH （6）；
n in the formulas (1) to (6) is a natural number and satisfies 2. ltoreq. n.ltoreq.60; m is a natural number and satisfies that m is more than or equal to 1 and less than or equal to 10; x1Has the structural formula of-O-R1-OH or-NH-R-OH, R1Is a divalent alkyl group containing a saturated carbon-oxygen chain.
6. The high abrasion resistant UV resin with fingerprint resistance function according to claim 1, wherein: in the mixture containing single-terminal carbon hydroxyl polysiloxane and double-terminal carbon hydroxyl polysiloxane:
the chemical formula of the single-end carbon hydroxyl polysiloxane is shown as the following formula (7):
a dicarbohydroxyl polysiloxane having the formula (8):
wherein,
in the above formulas (7) and (8):
R2and R3Is also a monovalent alkyl radical containing a saturated carbon-oxygen chain and having the formula CqH2q-1Wherein q is a natural number and satisfies 1. ltoreq. q.ltoreq.10;
X2has a structural formula of CH2(CH2)cCH2OCH2(CH2)dCH2；
a is a natural number and satisfies a condition that a is more than or equal to 2 and less than or equal to 100;
b is a natural number and satisfies that b is more than or equal to 2 and less than or equal to 100;
c is an integer and satisfies 0-10;
d is an integer and satisfies 0. ltoreq. d.ltoreq.10.
7. The high abrasion resistant UV resin with fingerprint resistance function according to claim 1, wherein: the linear polyester diol not containing fluorine and silicon is selected from one or more of aliphatic polyester diol, alicyclic polyester diol and aromatic polyester diol.
8. The high abrasion resistant UV resin with fingerprint resistance function according to claim 7, wherein: the aliphatic polyester diol is selected from one or more of polyethylene glycol adipate diol, polycarbonate diol and polypropylene glycol adipate diol;
the synthetic raw materials corresponding to the aliphatic ring in the alicyclic polyester diol structural unit are selected from one or more of cyclohexane dimethanol, cyclohexanediol, tricyclodecanedimethanol, dodecanediol and spiroglycol;
the synthetic raw materials corresponding to the aromatic ring in the aromatic polyester diol structural unit are selected from one or more of the combination of poly phthalic anhydride, methyl phthalic anhydride, phthalic acid, methyl phthalic acid, hydroquinone bis hydroxyethyl ether and resorcinol bis hydroxyethyl ether.
9. The high abrasion resistant UV resin with fingerprint resistance function according to claim 1, wherein: the functionality of the hydroxy acrylate containing a polyurethane structure is at least 5.
10. The high abrasion resistant UV resin with fingerprint resistance function according to claim 9, wherein: the hydroxyl acrylate containing a polyurethane structure is an equimolar ratio addition reaction product of a small molecular polyol compound and an acrylate compound containing an isocyanate group.
11. The high abrasion resistant UV resin with fingerprint resistance of claim 10, wherein: the small molecule polyol compound is selected from one or more of glycerol, butanetriol, hexanetriol, dipentaerythritol and tripentaerythritol.
12. The high abrasion resistant UV resin with fingerprint resistance of claim 10, wherein: the isocyanate group-containing acrylate compound has a functionality of 1.
13. A method for preparing the high abrasion resistant UV resin having anti-fingerprint function according to claim 1, wherein: the method comprises the following process steps:
step 1: diluting an isocyanate compound with isocyanate group functionality of 3 and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding perfluoropolyether alcohol with one end containing hydroxyl under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to obtain a solution containing an intermediate product 1, wherein the solid content of a reaction system is 10-70%;
step 2: diluting an isocyanate compound with isocyanate group functionality of 3 and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding single-end carbon hydroxyl polysiloxane under the stirring condition, and carrying out heat preservation reaction after the dripping is finished to prepare a solution containing an intermediate product 2, wherein the solid content of a reaction system is 10-70%;
and step 3: diluting an isocyanate compound with isocyanate group functionality of 2 and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dripping double-ended carbon hydroxyl polysiloxane under the condition of stirring, and carrying out heat preservation reaction after dripping is finished to prepare a solution containing an intermediate product 3, wherein the solid content of a reaction system is 10-70%;
and 4, step 4: uniformly mixing a solution containing an intermediate product 1, an intermediate product 2 and an intermediate product 3, heating under the protection of dry nitrogen, slowly dropwise adding linear polyester dihydric alcohol which does not contain fluorine and silicon under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to prepare a solution containing an intermediate product 4, wherein the solid content of a reaction system is 10-70%;
and 5: diluting a bifunctional isocyanate compound and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding a monohydroxy acrylate compound under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to obtain a solution containing an intermediate product 5, wherein the solid content of a reaction system is 10-70%;
step 6: diluting a small molecular polyol compound and a polyurethane reaction catalyst with a solvent, heating under the protection of dry nitrogen, slowly dropwise adding hydroxyl acrylate containing a polyurethane structure under the stirring condition, and carrying out heat preservation reaction after the dropwise adding is finished to obtain a solution containing an intermediate product 6, wherein the solid content of a reaction system is 10-70%;
and 7: under the conditions of dry nitrogen protection and stirring, heating the solution containing the intermediate product 4, then slowly dropwise adding the solution containing the intermediate product 6 into the solution containing the intermediate product 4, and carrying out heat preservation reaction after the dropwise adding is finished to obtain the solution containing the UV resin product, wherein the solid content of the product is 10-70%.
14. The method of claim 13, wherein:
the stirring speed during material dropping in the reaction systems of the step 1, the step 2, the step 3 and the step 4 is all 100-500 rpm, the material dropping time is all 1h-5h, the temperature during the heat preservation reaction is all 10-100 ℃, and the reaction time is all 1h-5 h;
the stirring speed during material dropping in the reaction systems of the step 5, the step 6 and the step 7 is 100-500 rpm, the material dropping time is 1-5 h, the temperature during the heat preservation reaction is 10-80 ℃, and the reaction time is 1-5 h.
15. The method of claim 13, wherein:
the molar ratio of the isocyanate group to the hydroxyl group in the reaction systems of the step 1 and the step 2 is 3: 1;
the molar ratio of the isocyanate group to the hydroxyl group in the reaction systems of the step 3 and the step 5 is 2: 1.
16. The method of claim 13, wherein:
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 1 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 2 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 3 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 5 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system;
the mass addition amount of the polyurethane reaction catalyst in the reaction system of the step 6 is 0.01-0.5% of the total mass of the reaction solid components in the reaction system.
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111057203A (en) * | 2019-12-31 | 2020-04-24 | 北京松井工程技术研究院有限公司 | Silicon-fluorine polyurethane acrylic resin and preparation method and application thereof |
| CN113136138A (en) * | 2021-05-13 | 2021-07-20 | 哈尔滨工业大学无锡新材料研究院 | Organic silicon hybrid polyurethane ultraviolet curing release agent and preparation method thereof |
| CN113201111A (en) * | 2021-06-21 | 2021-08-03 | 东莞三桐材料科技有限公司 | Fluorine-containing polyurethane acrylate resin, preparation method and application thereof |
| CN115717028A (en) * | 2022-12-06 | 2023-02-28 | 广东粤港澳大湾区黄埔材料研究院 | Oil-resistant and stain-resistant coating for vehicle clothes and preparation method thereof |
| CN115806760A (en) * | 2021-09-14 | 2023-03-17 | 北京化工大学 | Long-acting anti-fouling resin coating and preparation method thereof |
| CN115894938A (en) * | 2021-09-30 | 2023-04-04 | 浙江华峰新材料有限公司 | Carbon hydroxyl organic silicon polyether copolymer, polyurethane resin and preparation method thereof |
| CN116102969A (en) * | 2022-09-07 | 2023-05-12 | 江苏斯迪克新材料科技股份有限公司 | Fingerprint-resistant UV (ultraviolet) curing coating for film, preparation method of fingerprint-resistant UV curing coating and preparation method of film |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101544764A (en) * | 2008-03-26 | 2009-09-30 | Jsr株式会社 | Compound with poly-diakyl-polysiloxane group, curable composition and cured film containing the same |
| CN103483537A (en) * | 2013-09-26 | 2014-01-01 | 湖南本安亚大新材料有限公司 | UV curing resin, preparation method thereof and coating prepared therefrom |
| CN105385216A (en) * | 2015-12-23 | 2016-03-09 | 怀化学院 | UV photo-curing composition additive and preparation method thereof |
| CN105859997A (en) * | 2016-04-15 | 2016-08-17 | 江苏利田科技股份有限公司 | 3-functionality-degree polycaprolactone urethane acrylate and preparation method and application thereof |
| CN106220839A (en) * | 2016-08-04 | 2016-12-14 | 太仓中化环保化工有限公司 | A kind of anti-graffiti auxiliary agent of holo-fluorine polyester and preparation method thereof |
| CN106243969A (en) * | 2016-08-04 | 2016-12-21 | 太仓中化环保化工有限公司 | A kind of coating and preparation method thereof |
| CN106432686A (en) * | 2016-06-21 | 2017-02-22 | 衢州氟硅技术研究院 | Novel perfluoropolyether alkoxy silane compound and synthesis method thereof |
| CN106675383A (en) * | 2016-12-30 | 2017-05-17 | 江南大学 | Self-repairing type ultraviolet light cured anti-doodling resin and preparation method thereof |
| CN108034223A (en) * | 2017-12-12 | 2018-05-15 | 东莞市雄林新材料科技股份有限公司 | A kind of TPU film with anti-fingerprint oil-stain-preventing and preparation method thereof |
-
2021
- 2021-03-01 CN CN202110222736.3A patent/CN112574390B/en active Active
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101544764A (en) * | 2008-03-26 | 2009-09-30 | Jsr株式会社 | Compound with poly-diakyl-polysiloxane group, curable composition and cured film containing the same |
| CN103483537A (en) * | 2013-09-26 | 2014-01-01 | 湖南本安亚大新材料有限公司 | UV curing resin, preparation method thereof and coating prepared therefrom |
| CN105385216A (en) * | 2015-12-23 | 2016-03-09 | 怀化学院 | UV photo-curing composition additive and preparation method thereof |
| CN105859997A (en) * | 2016-04-15 | 2016-08-17 | 江苏利田科技股份有限公司 | 3-functionality-degree polycaprolactone urethane acrylate and preparation method and application thereof |
| CN106432686A (en) * | 2016-06-21 | 2017-02-22 | 衢州氟硅技术研究院 | Novel perfluoropolyether alkoxy silane compound and synthesis method thereof |
| CN106220839A (en) * | 2016-08-04 | 2016-12-14 | 太仓中化环保化工有限公司 | A kind of anti-graffiti auxiliary agent of holo-fluorine polyester and preparation method thereof |
| CN106243969A (en) * | 2016-08-04 | 2016-12-21 | 太仓中化环保化工有限公司 | A kind of coating and preparation method thereof |
| CN106675383A (en) * | 2016-12-30 | 2017-05-17 | 江南大学 | Self-repairing type ultraviolet light cured anti-doodling resin and preparation method thereof |
| CN108034223A (en) * | 2017-12-12 | 2018-05-15 | 东莞市雄林新材料科技股份有限公司 | A kind of TPU film with anti-fingerprint oil-stain-preventing and preparation method thereof |
Non-Patent Citations (1)
| Title |
|---|
| XIMING ZHONG等，: ""A novel UV/sunlight-curable anti-smudge coating system for various substrates"", 《CHEMICAL ENGINEERING JOURNAL》 * |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111057203A (en) * | 2019-12-31 | 2020-04-24 | 北京松井工程技术研究院有限公司 | Silicon-fluorine polyurethane acrylic resin and preparation method and application thereof |
| CN113136138A (en) * | 2021-05-13 | 2021-07-20 | 哈尔滨工业大学无锡新材料研究院 | Organic silicon hybrid polyurethane ultraviolet curing release agent and preparation method thereof |
| CN113201111A (en) * | 2021-06-21 | 2021-08-03 | 东莞三桐材料科技有限公司 | Fluorine-containing polyurethane acrylate resin, preparation method and application thereof |
| CN115806760A (en) * | 2021-09-14 | 2023-03-17 | 北京化工大学 | Long-acting anti-fouling resin coating and preparation method thereof |
| CN115806760B (en) * | 2021-09-14 | 2024-03-26 | 北京化工大学 | Long-acting anti-fouling resin coating and preparation method thereof |
| CN115894938A (en) * | 2021-09-30 | 2023-04-04 | 浙江华峰新材料有限公司 | Carbon hydroxyl organic silicon polyether copolymer, polyurethane resin and preparation method thereof |
| CN115894938B (en) * | 2021-09-30 | 2024-02-02 | 浙江华峰新材料有限公司 | Carbon hydroxyl organic silicon polyether copolymer, polyurethane resin and preparation method thereof |
| CN116102969A (en) * | 2022-09-07 | 2023-05-12 | 江苏斯迪克新材料科技股份有限公司 | Fingerprint-resistant UV (ultraviolet) curing coating for film, preparation method of fingerprint-resistant UV curing coating and preparation method of film |
| CN115717028A (en) * | 2022-12-06 | 2023-02-28 | 广东粤港澳大湾区黄埔材料研究院 | Oil-resistant and stain-resistant coating for vehicle clothes and preparation method thereof |
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