CN109504258B - 一种具有隔热和超疏水功能的透明车衣的制作方法 - Google Patents
一种具有隔热和超疏水功能的透明车衣的制作方法 Download PDFInfo
- Publication number
- CN109504258B CN109504258B CN201811322257.3A CN201811322257A CN109504258B CN 109504258 B CN109504258 B CN 109504258B CN 201811322257 A CN201811322257 A CN 201811322257A CN 109504258 B CN109504258 B CN 109504258B
- Authority
- CN
- China
- Prior art keywords
- component
- parts
- antimony oxide
- heat insulation
- car cover
- 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.)
- Active
Links
- 238000009413 insulation Methods 0.000 title claims abstract description 19
- 230000003075 superhydrophobic effect Effects 0.000 title claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- 239000003973 paint Substances 0.000 claims abstract description 33
- 239000000839 emulsion Substances 0.000 claims abstract description 31
- XXLJGBGJDROPKW-UHFFFAOYSA-N antimony;oxotin Chemical compound [Sb].[Sn]=O XXLJGBGJDROPKW-UHFFFAOYSA-N 0.000 claims abstract description 30
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000002131 composite material Substances 0.000 claims abstract description 19
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 19
- 239000011737 fluorine Substances 0.000 claims abstract description 19
- 229910000077 silane Inorganic materials 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 16
- 238000005507 spraying Methods 0.000 claims abstract description 12
- 238000001035 drying Methods 0.000 claims abstract description 9
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 7
- 239000004814 polyurethane Substances 0.000 claims description 14
- 229920002635 polyurethane Polymers 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 13
- 239000004970 Chain extender Substances 0.000 claims description 12
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 12
- 239000006185 dispersion Substances 0.000 claims description 12
- 229910052710 silicon Inorganic materials 0.000 claims description 12
- 239000010703 silicon Substances 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 10
- 239000004417 polycarbonate Substances 0.000 claims description 9
- 229920000515 polycarbonate Polymers 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- 239000002250 absorbent Substances 0.000 claims description 6
- 230000002745 absorbent Effects 0.000 claims description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 6
- 239000008367 deionised water Substances 0.000 claims description 6
- 229910021641 deionized water Inorganic materials 0.000 claims description 6
- 150000002009 diols Chemical class 0.000 claims description 6
- 230000003472 neutralizing effect Effects 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000002002 slurry Substances 0.000 claims description 6
- 239000000080 wetting agent Substances 0.000 claims description 6
- 230000001804 emulsifying effect Effects 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- QTRSWYWKHYAKEO-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-henicosafluorodecyl-tris(1,1,2,2,2-pentafluoroethoxy)silane Chemical compound FC(F)(F)C(F)(F)O[Si](OC(F)(F)C(F)(F)F)(OC(F)(F)C(F)(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 QTRSWYWKHYAKEO-UHFFFAOYSA-N 0.000 claims description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 4
- VCZJXEMVLNYRAS-UHFFFAOYSA-M sodium 1,4-diaminobutane-1-sulfonate Chemical compound [Na+].NCCCC(S(=O)(=O)[O-])N VCZJXEMVLNYRAS-UHFFFAOYSA-M 0.000 claims description 4
- VBGGLSWSRVDWHB-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-henicosafluorodecyl-tris(trifluoromethoxy)silane Chemical compound FC(F)(F)O[Si](OC(F)(F)F)(OC(F)(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 VBGGLSWSRVDWHB-UHFFFAOYSA-N 0.000 claims description 3
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 claims description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 3
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 3
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 3
- 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 3
- 229940089951 perfluorooctyl triethoxysilane Drugs 0.000 claims description 3
- ABTOQLMXBSRXSM-UHFFFAOYSA-N silicon tetrafluoride Chemical group F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 claims description 3
- AVYKQOAMZCAHRG-UHFFFAOYSA-N triethoxy(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane Chemical compound CCO[Si](OCC)(OCC)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F AVYKQOAMZCAHRG-UHFFFAOYSA-N 0.000 claims description 3
- DXODQEHVNYHGGW-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl-tris(trifluoromethoxy)silane Chemical compound FC(F)(F)O[Si](OC(F)(F)F)(OC(F)(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 DXODQEHVNYHGGW-UHFFFAOYSA-N 0.000 claims description 2
- LBTSNEJGMVFUEW-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,8,8,8-dodecafluorooctoxy-dimethoxy-propylsilane Chemical compound FC(C(C(C(C(F)(F)CO[Si](OC)(OC)CCC)(F)F)(F)F)(F)F)CC(F)(F)F LBTSNEJGMVFUEW-UHFFFAOYSA-N 0.000 claims description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 2
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 229960002887 deanol Drugs 0.000 claims description 2
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 2
- 239000012972 dimethylethanolamine Substances 0.000 claims description 2
- 238000006386 neutralization reaction Methods 0.000 claims description 2
- -1 polyoxypropylene Polymers 0.000 claims description 2
- DRRZZMBHJXLZRS-UHFFFAOYSA-N n-[3-[dimethoxy(methyl)silyl]propyl]cyclohexanamine Chemical compound CO[Si](C)(OC)CCCNC1CCCCC1 DRRZZMBHJXLZRS-UHFFFAOYSA-N 0.000 claims 1
- 229920001451 polypropylene glycol Polymers 0.000 claims 1
- 239000000463 material Substances 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 3
- 229910052797 bismuth Inorganic materials 0.000 description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000004922 lacquer Substances 0.000 description 3
- 229920005749 polyurethane resin Polymers 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000002612 dispersion medium Substances 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- JVYDLYGCSIHCMR-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butanoic acid Chemical compound CCC(CO)(CO)C(O)=O JVYDLYGCSIHCMR-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 230000003670 easy-to-clean Effects 0.000 description 1
- 230000009982 effect on human Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- XPBBUZJBQWWFFJ-UHFFFAOYSA-N fluorosilane Chemical compound [SiH3]F XPBBUZJBQWWFFJ-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000003760 hair shine Effects 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 150000003384 small molecules Chemical group 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005406 washing Methods 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- 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
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
-
- 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
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0828—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing sulfonate groups or groups forming them
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3212—Polyhydroxy compounds containing cycloaliphatic groups
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3228—Polyamines acyclic
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/34—Carboxylic acids; Esters thereof with monohydroxyl compounds
- C08G18/348—Hydroxycarboxylic acids
-
- 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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/44—Polycarbonates
-
- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6648—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38
- C08G18/6651—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38
-
- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6659—Compounds of group C08G18/42 with compounds of group C08G18/34
-
- 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
- C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
-
- 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
-
- 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
- C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
-
- 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
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
-
- 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
- C09D5/1687—Use of special additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2231—Oxides; Hydroxides of metals of tin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K3/2279—Oxides; Hydroxides of metals of antimony
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Manufacturing & Machinery (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
本发明公开了一种具有隔热和超疏水功能的透明车衣的制作方法,所述具有隔热和超疏水功能的透明车衣由A组分和B组分分别喷涂在车漆上烘干而制得,A组分和B组分的重量比为4‑100:1;其中,A组分为水性聚氨酯‑纳米氧化锡锑复合乳液,B组分为含氟硅烷溶液。使用时先将A组分均匀喷涂于车漆表面并烘干,然后喷涂B组分,在80‑150℃下加热1‑10分钟,即获得兼具隔热和超疏水效果的隐形车衣。
Description
技术领域
本发明涉及车漆保护膜技术领域,特别是涉及一种具有隔热和超疏水功能的透明车衣的制作方法。
背景技术
车辆在使用过程中难免发生剐蹭碰撞从而导致车漆损伤,长久的风吹日晒也会导致车漆老化、变色,为了保护车漆和提升美观,各类隐形车衣也应运而生。目前市场上主流的隐形车衣为TPU保护膜,如公开号为CN 206030690U的专利公开的一种汽车保护膜。此类保护膜贴膜时过程繁琐,耗时耗力,因接着车漆的保护膜最下层一般为热熔胶或压敏胶,对车漆附着力高,剥离时也非常繁琐,品质差的保护膜在剥离时容易残胶,甚至破坏漆面。因此,以水为分散介质的水性车衣开始逐渐占据市场,水性车衣使用简单,只需用喷枪将水性高分子材料均匀喷覆在车漆之上并烘干即可,省时省力。而且水性车衣直接在车漆上成膜,对车漆有一定附着力,又容易剥离,不会对车漆带来二次伤害,可以真正做到对车漆的保护,如公开号为CN 107501497A的专利所公开的一种车衣用水性聚氨酯树脂。膜类材料的另一个缺点为功能单一,不能针对不同要求作出调整。比如深色汽车漆容易吸热,在太阳直射时车内温度易升高,降温散热需要大量的能耗,一般保护膜却不能提供隔热的功能;汽车在存放行驶过程中也难免污损,每次洗车也需要耗费财力时间,但是市场上却没有针对此类问题等而推出的适用车衣。
发明内容
本发明的目的在于克服现有技术的不足,提供一种具有隔热和超疏水功能的透明车衣的制作方法,本发明以聚碳酸酯基水性聚氨酯树脂材料为成膜物,成膜后可提供对车漆适当的附着力和优异的隔绝保护性能,借助纳米氧化锡锑(ATO)对可视光(380nm~780nm)的吸收率极弱而且可以吸收或反射近红外线(1000nm~2500nm)的特性,将纳米氧化锡锑材料均匀分散在成膜物中从而获得兼具透明度和隔热性的隐形车衣,最后通过含氟硅烷和纳米氧化锡锑表面羟基的反应,赋予车衣优秀而持久的超疏水性能。
本发明由A组分和B组分分别喷涂在车漆上烘干而制得,A组分和B组分的重量比为4-100:1,使用时先将A组分均匀喷涂在车漆上并在25-70℃烘干,如此重复喷涂并且烘干3-8次,然后喷涂B组分,喷涂B组分后在80-150℃下加热1-10分钟;其中,
A组分为水性聚氨酯-纳米氧化锡锑复合乳液;
B组分为含氟硅烷溶液。
其中A组分水性聚氨酯-纳米氧化锡锑复合乳液的制备包括以下步骤,其中所用原料以质量份数计:
将相对分子质量为2000-3000的聚碳酸酯二元醇100份加入带控温和分散装置的密封分散釜中,依次加入脂肪族二异氰酸酯30-70份、催化剂0.05-0.2份、交联剂1-10份、小分子扩链剂0-28份、亲水扩链剂4-10份反应5-7小时,温度控制在50-85℃,然后降温至25-45℃,加入中和剂0-8份中和,加入去离子水高速搅拌乳化,制得固含量为30%-50%的水性聚氨酯乳液;
取上述制备的水性聚氨酯乳液100份加入带分散装置的密封分散釜中,加入有机硅流平剂0.1-1份,有机硅润湿剂0.1-1份,紫外线吸收剂0.5-3份,30%含量的纳米氧化锡锑浆10-50份,低速搅拌1小时,即得水性聚氨酯-纳米氧化锡锑复合乳液。
上述方法中所用的二异氰酸酯包括氢化二苯基甲烷二异氰酸酯、异氟尔酮二异氰酸酯、己二异氰酸酯中的至少一种;
上述方法中所用的催化剂包括有机铋催化剂和有机银催化剂中的至少一种;
上述方法中所用的交联剂包括三羟甲基丙烷和N303(相对分子质量为300的三羟基聚氧化丙醚)中的至少一种;
上述方法中所用的小分子扩链剂包括1,6-己二醇、1,4-丁二醇、1,4-环己基二甲醇中的至少一种;
上述方法中所用的亲水扩链剂包括2,2-二羟甲基丙酸、2,2-二羟甲基丁酸、2-(2-氨基乙基)氨基乙磺酸钠盐中的至少一种;
上述方法中所用的中和剂包括三乙胺、二甲基乙醇胺中的至少一种。
B组分全氟硅烷溶液由以下技术措施实现:
将含氟硅烷分散在溶剂中,均匀搅拌,制得固含量为1%-3%的含氟硅烷溶液。
上述方法中所用的含氟硅烷包括全氟癸基三乙氧基硅烷、十二氟庚基丙基甲基二甲氧基硅烷、十二氟庚基丙基三甲氧基硅烷、全氟癸基三甲氧基硅烷、全氟辛基三乙氧基硅烷、全氟辛基三甲氧基硅烷中的一种或者两种。
上述方法中所用的溶剂包括乙醇、异丙醇、丙酮、丁酮、碳酸二甲酯、N-甲基吡咯烷酮中的一种或者两种。本发明的有益效果是:
(1)本发明提供的具有隔热和超疏水功能的透明车衣以聚碳酸酯基水性聚氨酯树脂为主体原料,聚碳酸酯基水性聚氨酯耐老化性好、成膜强度高、韧性好、综合性能优异,配合各类助剂可以提供对车漆全方位的保护;
(2)本发明提供的主体原料以水为主要分散介质,对人体和环境无任何不良影响,除可用于车漆外,也可用于玻璃、透明塑料等材料的防护;
(3)纳米氧化锡锑材料的引入赋予车衣良好的隔热性能,在炎热天气可以减少降温所带来的能耗;
(4)本发明所用主体原料使用简单方便,相比贴膜工艺可以大大缩短施工时间,普通人也可在适宜条件下自行操作,而且其对车漆附着力不高,容易去除,无任何残胶,不会破坏车漆;
(5)纳米氧化锡锑表面有大量羟基,含氟硅烷溶液的溶剂会腐蚀聚氨酯材料表面,含氟硅烷水解后和纳米材料表面羟基接触并发生脱水缩合反应,使得大量含氟硅烷化学接枝在膜表面,从而获得持久的超疏水效果和一定的疏油效果,赋予车辆一定的自清洁性能,残留的少量污渍也很容易清洗干净。
具体实施方式
下面结合实施例进一步详细描述本发明的技术方案,但本发明的保护范围不局限于以下所述。
实施例1
本发明提供的一种具有隔热和超疏水功能的透明车衣,所述透明车衣由A组分和B组分分别喷涂在车漆上烘干而制得,A组分和B组分的重量比为4︰1,使用时先将A组分均匀喷涂在车漆上并在25℃条件下干燥,如此重复喷涂并干燥3次,然后喷涂B组分,喷涂B组分后在80℃下加热10分钟即得成品;其中,
A组分为水性聚氨酯-纳米氧化锡锑复合乳液;
B组分为含氟硅烷溶液。
上述A组分水性聚氨酯-纳米氧化锡锑复合乳液的制备依次经过以下步骤:
将相对分子质量为3000的聚碳酸酯二醇100份加入带加热、控温和分散装置的密封分散釜中,加入己二异氰酸酯70份,有机银催化剂0.2份,于80度反应2小时,然后加入N303 1份、环己基二甲醇28份反应2小时,降温至50度加入亲水扩链剂2-(2-氨基乙基)氨基乙磺酸钠5份反应1小时,然后降温至45度,加入去离子水高速搅拌乳化,制得固含量为30%的水性聚氨酯乳液;
取上述水性聚氨酯乳液100份,加入有机硅流平剂1份,有机硅润湿剂0.1份,紫外线吸收剂0.5份,30%含量的纳米氧化锡锑浆10份,以200r/min转速搅拌1小时,即得水性聚氨酯-纳米氧化锡锑复合乳液。
上述的B组分经过下述步骤制备:
将1份全氟癸基三乙氧基硅烷、2份十二氟庚基丙基甲基二甲氧基硅烷溶于97份乙醇中,制得固含量3%的含氟硅烷溶液。
本发明提供的具有隔热和超疏水功能的透明车衣韧性强、耐久性好、具有一定的隔热性能和良好的超疏水性能。
实施例2
本发明提供的一种具有隔热和超疏水功能的透明车衣,所述透明车衣由A组分和B组分分别喷涂在车漆上烘干而制得,A组分和B组分的重量比为100︰1,使用时先将A组分均匀喷涂在车漆上并在70℃条件下烘干,如此重复喷涂并干燥8次,然后喷涂B组分,喷涂B组分后在150℃下加热1分钟即得成品;其中,
A组分为水性聚氨酯-纳米氧化锡锑复合乳液;
B组分为含氟硅烷溶液。
上述A组分水性聚氨酯-纳米氧化锡锑复合乳液的制备依次经过以下步骤:
将相对质量分数为3000的聚碳酸酯二醇100份加入带加热、控温和分散装置的密封分散釜中,加入氢化二苯基甲烷二异氰酸酯30份, 有机铋催化剂0.05份于85度反应2小时,然后加入N303 10份反应2小时,然后降温至50度,加入亲水扩链剂2-(2-氨基乙基)氨基乙磺酸钠4份反应1小时,降温至25℃,加入去离子水高速搅拌乳化,制得固含量为50%的水性聚氨酯乳液;
取上述水性聚氨酯乳液100份,加入有机硅流平剂0.1份,有机硅润湿剂1份,紫外线吸收剂3份,30%含量的纳米氧化锡锑浆50份,以100r/min转速搅拌1小时,即得水性聚氨酯-纳米氧化锡锑复合乳液。
上述的B组分经过下述步骤制备:
将1份全氟癸基三甲氧基硅烷溶于99份异丙醇中,制得固含量1%的含氟硅烷溶液。
实施例3
本发明提供的一种具有隔热和超疏水功能的透明车衣,所述透明车衣由A组分和B组分分别喷涂在车漆上烘干而制得,A组分和B组分的重量比为20︰1,使用时先将A组分均匀喷涂在车漆上并在60℃条件下烘干,如此重复喷涂并干燥4次,然后喷涂B组分,喷涂B组分后在100℃下加热3分钟即得成品;其中,
A组分为水性聚氨酯-纳米氧化锡锑复合乳液;
B组分为含氟硅烷溶液。
上述A组分水性聚氨酯-纳米氧化锡锑复合乳液的制备依次经过以下步骤:
将相对质量分数为2000的聚碳酸酯二醇100份加入带加热、控温和分散装置的密封分散釜中,加入异氟尔酮二异氰酸酯60份, 有机铋催化剂0.1份于85度反应2小时,然后加入三羟甲基丙烷2份、1,4-丁二醇5份反应2小时,然后加入亲水扩链剂2,2-二羟甲基丙酸10份反应3小时,降温至35℃,加入三乙胺8份充分中和,然后加入去离子水高速搅拌乳化,制得固含量为35%的水性聚氨酯乳液;
取上述水性聚氨酯乳液100份,加入有机硅流平剂0.5份,有机硅润湿剂0.5份,紫外线吸收剂2份,30%含量的纳米氧化锡锑浆30份,以500r/min转速搅拌1小时,即得水性聚氨酯-纳米氧化锡锑复合乳液。
上述的B组分经过下述步骤制备:
将2份全氟辛基三乙氧基硅烷溶于98份异丙醇中,制得固含量2%的含氟硅烷溶液。
实施例4
本发明提供的一种具有隔热和超疏水功能的透明车衣,所述透明车衣由A组分和B组分分别喷涂在车漆上烘干而制得,A组分和B组分的重量比为40︰1,使用时先将A组分均匀喷涂在车漆上并在50℃条件下烘干,如此重复喷涂并干燥6次,然后喷涂B组分,喷涂B组分后在120℃下加热2分钟即得成品;其中,
A组分为水性聚氨酯-纳米氧化锡锑复合乳液;
B组分为含氟硅烷溶液。
上述A组分水性聚氨酯-纳米氧化锡锑复合乳液的制备依次经过以下步骤:
将相对质量分数为2000的聚碳酸酯二醇100份加入带加热、控温和分散装置的密封分散釜中,加入氢化二苯基甲烷二异氰酸酯40份, 有机铋催化剂0.05份于85度反应2小时,然后加入N303 2份、1,6-己二醇1份反应1小时,然后加入亲水扩链剂2,2-二羟甲基丁酸8份反应3小时,降温至30℃,加入三乙胺6份充分中和,然后加入去离子水高速搅拌乳化,制得固含量为40%的水性聚氨酯乳液;
取上述水性聚氨酯乳液100份,加入有机硅流平剂0.3份,有机硅润湿剂0.6份,紫外线吸收剂2.5份,30%含量的纳米氧化锡锑浆20份,以300r/min转速搅拌1小时,即得水性聚氨酯-纳米氧化锡锑复合乳液。
上述的B组分经过下述步骤制备:
将2.5份全氟癸基三乙氧基硅烷溶于97.5份异丙醇中,制得固含量2.5%的含氟硅烷溶液。
尽管本发明已进行了一定程度的描述,明显地,在不脱离本发明的精神和范围的条件下,可进行各个条件的适当变化。可以理解,本发明不限于所述实施方案,而归于权利要求的范围,其包括所述每个因素的等同替换。
Claims (2)
1.一种具有隔热和超疏水功能的透明车衣的制作方法,其特征在于,由A组分和B组分分别喷涂在车漆上烘干而制得,A组分和B组分的重量比为4-100:1,使用时先将A组分均匀喷涂在车漆上并在25-70℃烘干,如此重复3-8次,然后喷涂B组分,喷涂B组分后在80-150℃下加热1-10分钟;其中,
A组分为水性聚氨酯-纳米氧化锡锑复合乳液;
B组分为含氟硅烷溶液;
所述A组分水性聚氨酯-纳米氧化锡锑复合乳液的制备方法包括以下步骤,其中所用原料以质量份数计:
将相对分子质量为2000-3000的聚碳酸酯二元醇100份加入带控温和分散装置的密封分散釜中,依次加入脂肪族二异氰酸酯30-70份、催化剂0.05-0.2份、交联剂1-10份、小分子扩链剂0-28份、亲水扩链剂4-10份,温度控制在50-85℃共反应5-7小时,然后降温至25-45℃,加入中和剂0-8份中和,加入去离子水高速搅拌乳化,制得固含量为30%-50%的水性聚氨酯乳液;
取上述制备的水性聚氨酯乳液100份加入带分散装置的密封分散釜中,加入有机硅流平剂0.1-1份,有机硅润湿剂0.1-1份,紫外线吸收剂0.5-3份,30%含量的纳米氧化锡锑浆10-50份,以100-500r/min转速搅拌1小时,即得水性聚氨酯-纳米氧化锡锑复合乳液;
所述脂肪族二异氰酸酯包括异氟尔酮二异氰酸酯、己二异氰酸酯中的至少一种;
所述催化剂包括有机铋催化剂和有机银催化剂中的至少一种;
所述交联剂包括三羟甲基丙烷和相对分子质量为300的三羟基聚氧化丙醚中的至少一种;
所述小分子扩链剂包括1,6-己二醇、1,4-丁二醇、1,4-环己基二甲醇中的至少一种;
所述亲水扩链剂包括2,2-二羟甲基丙酸、2,2-二羟甲基丁酸、2-(2-氨基乙基)氨基乙磺酸钠盐中的至少一种;
所述中和剂包括三乙胺、二甲基乙醇胺中的至少一种;
所述B组分全氟硅烷溶液由含氟硅烷和溶剂组成,所述全氟硅烷溶液固含量为1%-3%;
所述含氟硅烷包括全氟癸基三乙氧基硅烷、十二氟庚基丙基甲基二甲氧基硅烷、十二氟庚基丙基三甲氧基硅烷、全氟癸基三甲氧基硅烷、全氟辛基三乙氧基硅烷、全氟辛基三甲氧基硅烷中的一种或者两种。
2.根据权利要求1所述的一种具有隔热和超疏水功能的透明车衣的制作方法,其特征在于,所述溶剂包括乙醇、异丙醇、丙酮、丁酮、碳酸二甲酯、N-甲基吡咯烷酮中的一种或者两种。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811322257.3A CN109504258B (zh) | 2018-11-08 | 2018-11-08 | 一种具有隔热和超疏水功能的透明车衣的制作方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811322257.3A CN109504258B (zh) | 2018-11-08 | 2018-11-08 | 一种具有隔热和超疏水功能的透明车衣的制作方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN109504258A CN109504258A (zh) | 2019-03-22 |
CN109504258B true CN109504258B (zh) | 2020-11-03 |
Family
ID=65747766
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201811322257.3A Active CN109504258B (zh) | 2018-11-08 | 2018-11-08 | 一种具有隔热和超疏水功能的透明车衣的制作方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109504258B (zh) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111574822B (zh) * | 2020-06-04 | 2022-03-01 | 北京浦江兄弟科技有限公司 | 一种聚氨酯疏水薄膜、制备方法及其用途 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101537682B (zh) * | 2009-03-16 | 2011-06-29 | 浙江工业大学 | 一种纳米颗粒辅助微模塑制备超疏水表面的方法 |
CN103333600B (zh) * | 2013-05-30 | 2016-12-28 | 中国科学院合肥物质科学研究院 | 一种单组份水性聚氨酯透明隔热涂料的制备方法 |
CN105032731B (zh) * | 2015-08-05 | 2018-12-28 | 北京航空航天大学 | 一种超疏水涂层与加热涂层复合的节能防除冰涂层制备方法 |
CN105647245B (zh) * | 2016-01-27 | 2018-08-31 | 柳州豪祥特科技有限公司 | 纳米ato隔热有机涂层的制备工艺 |
-
2018
- 2018-11-08 CN CN201811322257.3A patent/CN109504258B/zh active Active
Also Published As
Publication number | Publication date |
---|---|
CN109504258A (zh) | 2019-03-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3971872A (en) | Process for the production of an abrasion resistant optical element | |
CN111607320B (zh) | 一种水性聚氨酯-硅溶胶复合防雾剂及其制备方法和应用 | |
CN109517513B (zh) | 一种具有自消光效果的常温自修复型水性聚氨酯车衣的制作方法 | |
CN106821796B (zh) | 一种生物基水性uv固化环保指甲油的制备方法 | |
CN101939389B (zh) | 塑料基材用涂料组合物、由其形成的涂膜、以及成形体 | |
JP5653884B2 (ja) | 紫外線・近赤外線遮断水性塗料、該塗料からなる塗膜が形成された遮熱処理ガラス及び該塗料を用いた窓ガラスの遮熱処理方法 | |
CN112920699B (zh) | 一种基于金属配位作用的水性自修复聚氨酯涂层及其制备方法 | |
CN104926156A (zh) | 一种透明持久型防雾玻璃的制备方法及其制品 | |
CN109705755A (zh) | 一种pu保护膜及其生产涂布工艺 | |
US5891261A (en) | Method of stripping a strippable coating film | |
KR101853888B1 (ko) | 고신율/고경도 하드코팅 조성물 및 코팅 필름 | |
CN109504258B (zh) | 一种具有隔热和超疏水功能的透明车衣的制作方法 | |
CN113072890A (zh) | 一种自修复耐黄变型漆面保护膜及其制备方法 | |
CN106366898B (zh) | 一种紫外线光固化防雾涂料及其制备方法 | |
CN101511921A (zh) | 具有聚氨酯底漆的车窗面板 | |
CN110358375A (zh) | 一种耐刮擦的氟碳层涂布液及使用该涂布液的太阳能背板 | |
CN108977026A (zh) | 一种耐磨水性聚氨酯涂料及其制备方法 | |
CN114958186A (zh) | 一种光伏板透明长效易清洁阻燃抗污涂层的制备方法及应用 | |
CN114133491A (zh) | 一种光学级疏水疏油型热修复树脂及其制备方法和自修复涂层 | |
CN101864217B (zh) | Pet膜用氟碳涂料及其制备方法和应用 | |
CN110970173B (zh) | 一种可定制图案的纳米银线透明导电膜的制作方法 | |
CN109957322B (zh) | 一种双交联固化防雾薄膜及其制备方法 | |
CN115418144B (zh) | 超低醇解度聚乙烯醇防雾涂膜材料及其制造方法 | |
CN103664003A (zh) | 一种隔热防雾膜剂的制备方法 | |
CN106519170B (zh) | 一种木器漆修色用水性聚氨酯树脂及其制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |