CN107972331B - A kind of preparation method of automobile thermal insulation, sun-shade pad - Google Patents
A kind of preparation method of automobile thermal insulation, sun-shade pad Download PDFInfo
- Publication number
- CN107972331B CN107972331B CN201711301148.9A CN201711301148A CN107972331B CN 107972331 B CN107972331 B CN 107972331B CN 201711301148 A CN201711301148 A CN 201711301148A CN 107972331 B CN107972331 B CN 107972331B
- Authority
- CN
- China
- Prior art keywords
- sun
- thermal insulation
- coating
- heat
- resistant layer
- 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.)
- Expired - Fee Related
Links
- 238000009413 insulation Methods 0.000 title claims abstract description 54
- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- 239000011248 coating agent Substances 0.000 claims abstract description 85
- 238000000576 coating method Methods 0.000 claims abstract description 85
- 239000000835 fiber Substances 0.000 claims abstract description 58
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229920000728 polyester Polymers 0.000 claims abstract description 17
- 229920006231 aramid fiber Polymers 0.000 claims abstract description 11
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 8
- 239000007921 spray Substances 0.000 claims abstract description 7
- 238000001035 drying Methods 0.000 claims abstract description 6
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 6
- 238000009954 braiding Methods 0.000 claims abstract description 4
- 238000001465 metallisation Methods 0.000 claims abstract description 4
- 238000007747 plating Methods 0.000 claims abstract description 4
- 239000000463 material Substances 0.000 claims description 38
- 239000011490 mineral wool Substances 0.000 claims description 37
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 30
- 239000012782 phase change material Substances 0.000 claims description 30
- 239000010439 graphite Substances 0.000 claims description 29
- 229910002804 graphite Inorganic materials 0.000 claims description 29
- 239000000843 powder Substances 0.000 claims description 29
- 239000000758 substrate Substances 0.000 claims description 29
- 230000008859 change Effects 0.000 claims description 21
- 239000012071 phase Substances 0.000 claims description 21
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims description 20
- 239000007791 liquid phase Substances 0.000 claims description 20
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 15
- 239000004917 carbon fiber Substances 0.000 claims description 15
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 239000010445 mica Substances 0.000 claims description 12
- 229910052618 mica group Inorganic materials 0.000 claims description 12
- 229910000314 transition metal oxide Inorganic materials 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000002270 dispersing agent Substances 0.000 claims description 11
- 229910021485 fumed silica Inorganic materials 0.000 claims description 10
- 230000007704 transition Effects 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 239000006185 dispersion Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 238000003860 storage Methods 0.000 claims description 5
- PRPAGESBURMWTI-UHFFFAOYSA-N [C].[F] Chemical compound [C].[F] PRPAGESBURMWTI-UHFFFAOYSA-N 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 claims description 3
- 239000003292 glue Substances 0.000 claims description 3
- 238000000465 moulding Methods 0.000 claims description 3
- 239000000565 sealant Substances 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 1
- 229960000583 acetic acid Drugs 0.000 claims 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 claims 1
- 239000012258 stirred mixture Substances 0.000 claims 1
- 239000002966 varnish Substances 0.000 abstract description 11
- 230000000694 effects Effects 0.000 abstract description 9
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 abstract description 8
- 230000036760 body temperature Effects 0.000 abstract description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 24
- 239000000194 fatty acid Substances 0.000 description 24
- 229930195729 fatty acid Natural products 0.000 description 24
- 150000004665 fatty acids Chemical class 0.000 description 24
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 22
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 16
- 230000005496 eutectics Effects 0.000 description 16
- 235000012245 magnesium oxide Nutrition 0.000 description 12
- 239000000395 magnesium oxide Substances 0.000 description 11
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 9
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 9
- 239000005639 Lauric acid Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 7
- 235000021360 Myristic acid Nutrition 0.000 description 7
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229910001369 Brass Inorganic materials 0.000 description 6
- 239000010951 brass Substances 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- 239000000499 gel Substances 0.000 description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 238000002310 reflectometry Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 206010053615 Thermal burn Diseases 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- 239000004411 aluminium Substances 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 230000017525 heat dissipation Effects 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229920004933 Terylene® Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- MFUVDXOKPBAHMC-UHFFFAOYSA-N magnesium;dinitrate;hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MFUVDXOKPBAHMC-UHFFFAOYSA-N 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 238000004321 preservation Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 244000147568 Laurus nobilis Species 0.000 description 1
- 235000017858 Laurus nobilis Nutrition 0.000 description 1
- 208000037656 Respiratory Sounds Diseases 0.000 description 1
- 241000220287 Sedum rubrotinctum Species 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 235000005212 Terminalia tomentosa Nutrition 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- -1 acrylic ester Chemical class 0.000 description 1
- 239000002156 adsorbate Substances 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 229960000935 dehydrated alcohol Drugs 0.000 description 1
- 208000002173 dizziness Diseases 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000010721 machine oil Substances 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002905 metal composite material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001007 puffing effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
- B32B5/08—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer the fibres or filaments of a layer being of different substances, e.g. conjugate fibres, mixture of different fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/067—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of fibres or filaments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
- B32B3/02—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by features of form at particular places, e.g. in edge regions
- B32B3/08—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by features of form at particular places, e.g. in edge regions characterised by added members at particular parts
- B32B3/085—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by features of form at particular places, e.g. in edge regions characterised by added members at particular parts spaced apart pieces on the surface of a layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
- B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
- B32B3/30—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by a layer formed with recesses or projections, e.g. hollows, grooves, protuberances, ribs
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B33/00—Layered products characterised by particular properties or particular surface features, e.g. particular surface coatings; Layered products designed for particular purposes not covered by another single class
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60J—WINDOWS, WINDSCREENS, NON-FIXED ROOFS, DOORS, OR SIMILAR DEVICES FOR VEHICLES; REMOVABLE EXTERNAL PROTECTIVE COVERINGS SPECIALLY ADAPTED FOR VEHICLES
- B60J11/00—Removable external protective coverings specially adapted for vehicles or parts of vehicles, e.g. parking covers
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/65—Additives macromolecular
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/70—Additives characterised by shape, e.g. fibres, flakes or microspheres
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/06—Materials undergoing a change of physical state when used the change of state being from liquid to solid or vice versa
- C09K5/063—Materials absorbing or liberating heat during crystallisation; Heat storage materials
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/77—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
- D06M11/79—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/83—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with metals; with metal-generating compounds, e.g. metal carbonyls; Reduction of metal compounds on textiles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/06—Coating on the layer surface on metal layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/26—Polymeric coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/02—Synthetic macromolecular fibres
- B32B2262/0261—Polyamide fibres
- B32B2262/0269—Aromatic polyamide fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/02—Synthetic macromolecular fibres
- B32B2262/0276—Polyester fibres
- B32B2262/0284—Polyethylene terephthalate [PET] or polybutylene terephthalate [PBT]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/14—Mixture of at least two fibres made of different materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/30—Properties of the layers or laminate having particular thermal properties
- B32B2307/304—Insulating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/30—Properties of the layers or laminate having particular thermal properties
- B32B2307/306—Resistant to heat
- B32B2307/3065—Flame resistant or retardant, fire resistant or retardant
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/40—Properties of the layers or laminate having particular optical properties
- B32B2307/416—Reflective
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/582—Tearability
- B32B2307/5825—Tear resistant
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2605/00—Vehicles
- B32B2605/08—Cars
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/32—Polyesters
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/34—Polyamides
- D06M2101/36—Aromatic polyamides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Textile Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Mechanical Engineering (AREA)
- Inorganic Chemistry (AREA)
- Laminated Bodies (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Thermal Insulation (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
The invention discloses a kind of preparation methods of automobile thermal insulation, sun-shade pad, the following steps are included: step 1, braiding high-strength yarn, aramid fiber is merged into twisting into high-strength yarn for 2:1 according to mass percent with polyester fiber, high-strength yarn is then woven into tear resistant layer;Obtained tear resistant layer is immersed in silica solution by step 2, is then allowed to stand carry out gel, and taking-up, which is put into 60 DEG C of thermostatic drying chambers, after 10h is dried, and the tear resistant layer after obtaining Gel Treatment is spare;Step 3, the face jet-plating metallization reflectance coating in tear resistant layer, then spray fluorocarbon varnish on the metallic reflective coating of formation, spare and etc. after dry.Thermal insulation, sun-shade pad significant effect produced by the present invention can make vehicle interior temperature maintain 36 DEG C or less (generally at 33 DEG C or so) at 30 DEG C of temperature, vehicle body temperature maintains 39 DEG C or less (generally at 35 DEG C or so), and overall thickness is no more than 1cm, foldable, carry easy to use, application easy to spread.
Description
The application is title are as follows: a kind of automobile thermal insulation, sun-shade pad, application No. is: 201610814021.6 patent of invention
Divisional application, parent application day be on 09 09th, 2016.
Technical field
The present invention relates to automobile sun-shadings to pad technical field, in particular to a kind of preparation method of automobile thermal insulation, sun-shade pad.
Background technique
For automobile as people's outdoor activities tool, the probability by extraneous strong illumination is very high, and the time is especially long, especially
It is the arriving with torridity summer, the vehicle of many people is parked on open parking ground, by being exposed to the sun, when people turn again to car
When, vehicle interior temperature is odd high, and people can not endure at all, by field observation, in Sichuan Province, sunny one day, Chengdu, works as the external world
When temperature is 32 DEG C, after the automobile of no sun-shade cushion is parked in open parking ground 1 hour, with thermometer measure vapour vehicle interior temperature, survey
Testing result is, interior cabin temperature reaches 65 DEG C, is higher by 33 DEG C than outside air temperature, and at this temperature, people can only first open
Interior air-conditioning could into the car after for a period of time, this not only time consumption and energy consumption source, can also happen suddenly fortuitous event, and dizziness is caused to vomit
It spits or even falls in a swoon, the harm such as self-burning of vehicle, meanwhile, through testting, the temperature of automobile metal body portion can reach 75 DEG C or more, pole
Easily cause scald.
Therefore, in recent years it has been developed that various types of products are used for automobile cooling, mainly with awning, glass
Heat insulation type adhering film and thermal insulation, sun-shade pad are main product, and since thermal insulation, sun-shade pad carries and uses conveniently, price is lower, heat insulation
It is good, like by people always.It is claimed according to certain famous thermal insulation, sun-shade pad manufacturing enterprise, after thermal insulation, sun-shade pad, automobile interior exterior
Temperature difference within 12 DEG C, generally between 6-7 DEG C, i.e., when outdoor temperature be 32 DEG C when, be capped with thermal insulation, sun-shade pad
For temperature in automobile generally at 38 DEG C or so, highest does not exceed 44 DEG C, has outstanding heat insulation.
But the existing automobile heat insulation sun-shade cushion used remains not perfect place, heat-insulated approach can only be by anti-
Sunlight is penetrated to realize, and cooling cannot be thermally shielded to vehicle body, therefore there is also the larger rising spaces for its heat-insulating capability.Namely
It is to say, existing thermal insulation, sun-shade pad often has ignored the heat absorption of vehicle body itself, even if vehicle interior temperature differs 6 DEG C with outside air temperature, gold
The temperature for belonging to vehicle body then at least differs 13 DEG C or more, especially black paint vehicle body, and temperature can reach 20 DEG C of difference, still suffer from
A possibility that scalding, heat insulation need to be improved.
Summary of the invention
Goal of the invention of the invention is: in view of the above problems, providing a kind of system of automobile thermal insulation, sun-shade pad
Preparation Method, with bad, the interior and higher problem of vehicle body temperature that solves existing thermal insulation, sun-shade pad heat insulation.
The technical solution adopted by the invention is as follows: a kind of automobile thermal insulation, sun-shade pad, is successively bonded with metal from top to bottom
Reflectance coating, tear resistant layer, mineral wool structure sheaf and flexible heat-conducting layer, one side of the metallic reflective coating far from tear resistant layer uniformly coat
Have fluorocarbon varnish, tear resistant layer is woven with high-strength yarn, mineral wool structure sheaf with flexible heat-conducting layer is Nian Jie sets on one side
There are several cone substrates, phase-change material is full of in cone substrate, flexible heat-conducting layer is Nian Jie with mineral wool structure sheaf by adhesive coating.
Due to the setting of above structure, metallic reflective coating for reflecting back most sunlights, use by fluorocarbon varnish
In protection metallic reflector;On the one hand tear resistant layer is used to improve the mechanical strength and durability of thermal insulation, sun-shade pad, on the other hand
Energy for obstructing sunlight carrying infiltrates into inside thermal insulation, sun-shade pad, and then plays heat-blocking action;Mineral wool structure sheaf one
Aspect is for heat-insulated, on the other hand for providing storage organization and fixed flexible heat-conducting layer for phase-change material;Flexible heat-conducting layer is used
In carrying out heat radiator to vehicle body, to reduce the temperature in vehicle society;Phase-change material layers for reducing flexible heat-conducting layer heat dynamic
Equilibrium temperature keeps cooling effect more significant.
Further, high-strength yarn is twisted by aramid fiber and polyester fiber merging, wherein aramid fiber and terylene
The mass percent of fiber is 2:1.
Further, adhesive coating is covered in the one side with cone substrate of mineral wool structure sheaf.
Further, cone substrate is conic tower type dome structure, is evenly distributed on mineral wool structure sheaf, the height for boring substrate is
0.2-5mm。
Further, fluorocarbon varnish coating thickness is 150-300 μm, and metallic reflective coating sputter is flexible with a thickness of 50-150 μm
Heat-conducting layer with a thickness of 0.6-1mm.
Further, flexible heat-conducting layer is made of flexible heat-conductive coating, and flexible heat-conductive coating is by weight by following raw material
Composition: 38 parts of organosilicon modified crylic acid resin, 8 parts of expanded graphite, 14 parts of heat conducting fiber silk, 6 parts of mica powder, transition metal is multiple
Close 6 parts of oxide powder, 10 parts of butyl acetate, 0.7 part of fumed silica, 15 parts of diacetone alcohol, 1.3 parts of dispersing agent and levelling
0.7 part of agent.
Further, phase-change material is solid-liquid phase change material, and the phase transition temperature of solid-liquid phase change material is 31-36 DEG C.
The invention also includes a kind of preparation methods of automobile thermal insulation, sun-shade pad, comprising the following steps:
Step 1, braiding high-strength yarn, by 42-58 root aramid fiber and 21-29 root polyester fiber according to mass percent
Merge twisting into high-strength yarn for 2:1, high-strength yarn is then woven into tear resistant layer;
Obtained tear resistant layer is immersed in silica solution by step 2, is then allowed to stand carry out gel, is taken out after 10h and be put into 60
It is dried in DEG C thermostatic drying chamber, the tear resistant layer after obtaining Gel Treatment is spare;
Then step 3, the face jet-plating metallization reflectance coating in tear resistant layer spray fluorine carbon on the metallic reflective coating of formation
Varnish, it is spare after dry;
Mineral wool is pressed into mineral wool structure sheaf of the one side with cone substrate by step 4, manufacture mineral wool molding die,
It is spare;
Step 5, the face spray containment glue that cone substrate is had in mineral wool structure sheaf, and on the face of mineral wool structure sheaf
One layer of sealant is formed, it is spare after dry;
Step 6, manufacture solid-liquid phase change material, become liquid phase for solid-liquid phase change material heating and are placed on mineral wool structure sheaf
Cone substrate in, wherein bore intrabasement liquid phase phase-change material depth be no more than cone substrate height, then by glass cotton knot
Structure is placed on that vacuum tank is hollow to be cooled to room temperature;
Step 7 manufactures flexible heat-conductive coating, organosilicon modified crylic acid resin and dispersing agent is added in reactor, so
Mixed component is stirred up to being uniformly dispersed with the revolving speed of 800r/min with blender afterwards, base-material is obtained, then to base-material
In sequentially add carbon fiber wire, expanded graphite, mica powder, fumed silica, compound transition metal oxide powder, then plus
Enter butyl acetate and diacetone alcohol, mixture is sufficiently stirred with blender, mixing speed 1000r/min, until point
It dissipates uniformly, obtains initial point;
Metal fiber wire and levelling agent are added in the initial point of step 7 step 8, after being uniformly dispersed with dispersion machine
To uncured coating, uncured coating is pumped into the storage tank of air gun, is then sprayed on step 6 with air gun
One side of the obtained mineral wool structure sheaf with cone substrate, stands to coating levelling, is put into high temperature oven vacuum at 140 DEG C
Baking-curing film forming, then keeps the temperature 10min again, cools to room temperature with the furnace, obtain initial thermal insulation, sun-shade pad;
Step 9, tear resistant layer that step 3 obtains is obtained with step 7 without the one side of metallic reflective coating it is initial heat-insulated
Sun-shade cushion be adhesively fixed without the one side of flexible heat-conductive coating with binder after to get to thermal insulation, sun-shade pad.
In conclusion by adopting the above-described technical solution, the beneficial effects of the present invention are:
1, thermal insulation, sun-shade of the invention pad raw material sources are extensive, and it is convenient that the processing is simple, and manufacturing cost is low, are suitable for industrial big
Large-scale production;
2, tear resistant layer is worked out with high-strength yarn, can greatly improve the mechanical strength of thermal insulation, sun-shade pad, simultaneously
After tear resistant layer is impregnated with silica solution, it is filled with Silica hydrogel in gap, there is significant heat-proof quality, flame retardant property and prevents
Aqueous energy, improves the quality of thermal insulation, sun-shade pad on the whole;
3, the setting of flexible heat-conducting layer and phase-change material, makes thermal insulation, sun-shade pad not only have the function of thermal insulation, sun-shade, also has
There is heat radiator effect, the temperature of vehicle body can be greatly reduced, the temperature of vehicle body is made to maintain the wind for avoiding scald compared with low state
Danger, further improves the performance of thermal insulation, sun-shade pad;
4, thermal insulation, sun-shade of the invention pad significant effect can make vehicle interior temperature maintain 36 DEG C or less at 30 DEG C of temperature
(generally at 33 DEG C or so), vehicle body temperature maintain 39 DEG C or less (generally at 35 DEG C or so), and overall thickness is no more than 1cm, can roll over
It is folded, carry easy to use, application easy to spread.
Detailed description of the invention
Fig. 1 is a kind of thermal insulation, sun-shade mat structure schematic diagram of the invention;
Fig. 2 is the partial structurtes enlarged diagram of part A in Fig. 1;
Fig. 3 is flexible heat-conducting layer Part portions structure enlargement diagram.
Marked in the figure: 1 is fluorocarbon varnish, 2 be metallic reflective coating, and 3 be tear resistant layer, and 4 be mineral wool structure sheaf, and 5 be phase
Become material, 6 be flexible heat-conducting layer, and 61 be metal fiber wire, and 62 be carbon fiber wire, and 63 be expanded graphite, and 64 is multiple for transition metal
Oxide powder is closed, 7 be adhesive coating.
Specific embodiment
With reference to the accompanying drawing, the present invention is described in detail.
In order to make the objectives, technical solutions, and advantages of the present invention clearer, with reference to the accompanying drawings and embodiments, right
The present invention is further elaborated.It should be appreciated that the specific embodiments described herein are merely illustrative of the present invention, and
It is not used in the restriction present invention.
Embodiment one
As depicted in figs. 1 and 2, a kind of automobile thermal insulation, sun-shade pad is successively bonded with metallic reflective coating 2 from top to bottom, resists
Tearing layer 3, mineral wool structure sheaf 4 and flexible heat-conducting layer 6, metallic reflective coating 2 are uniformly coated with fluorine far from the one side of tear resistant layer 3
Carbon varnish 1, tear resistant layer 3 are woven with high-strength yarn, mineral wool structure sheaf 4 with flexible heat-conducting layer 6 is Nian Jie sets on one side
There are several cone substrates, phase-change material 5 is full of in cone substrate, flexible heat-conducting layer 6 is viscous by adhesive coating 7 and mineral wool structure sheaf
It connects.
Mineral wool structure sheaf 4, mineral wool has thermal insulation function well, while also having toughness and stabilization well
Property, when this is used for thermal insulation, sun-shade pad, good heat insulation and preservation effect on the one hand can be played, on the other hand can be enhanced heat-insulated
The mechanical property of sun-shade cushion, it is more stable to be allowed to structure, is not susceptible to deform.The one side setting cone substrate of mineral wool structure sheaf 4
Cause be, on the one hand make bore substrate in fill phase-change material 5, on the other hand make bore substrate protrusion part and flexible heat-conducting layer
6 connections, flexible heat-conducting layer 6, which is firmly combined, to be not easily disconnected from.Furthermore, cone substrate is conic tower type dome structure, is uniformly divided
For cloth on mineral wool structure sheaf 4, it is preferably 0.2mm that the height for boring substrate, which is 0.2-5mm(, and 0.2mm or 5mm also may be selected).
Tear resistant layer 3 is woven with high-strength yarn, and high-strength yarn merges twisting by aramid fiber and polyester fiber
It forms, aramid fiber has the features such as elongation is high, and pulling force is strong, thermal resistance and acid-alkali resistance, and terylene is high with intensity, elasticity is good, heat-resisting resistance to
The features such as soda acid, the two was applied in combination, and had complementary advantages, and making high-strength yarn not only has good stability, also had height
The elasticity and tear resistance of intensity, intensity is high, not tearable.Furthermore, the quality hundred of aramid fiber and polyester fiber
Divide than being 2:1, so that high-strength yarn mainly has the advantageous feature of aramid fiber.
Flexible heat-conducting layer 6, to carry out heat radiator to vehicle body, reduces the temperature of vehicle body, more for directly contacting with vehicle body
It further says, flexible heat-conducting layer 6 is made of flexible heat-conductive coating, and flexible heat-conductive coating is by weight by following raw material group
At: 34-39 parts of organosilicon modified crylic acid resin, 7-9 parts of expanded graphite, 12-15 parts of heat conducting fiber silk, 6-8 parts of mica powder, mistake
Cross 5-7 parts of metal compound oxide powder, 9-11 parts of butyl acetate, 0.5-1 parts of fumed silica, 12-17 parts of diacetone alcohol,
1-1.5 parts and levelling agent 0.5-1 parts of dispersing agent.
In the present embodiment, flexible heat-conductive coating can be made of the raw material of following parts by weight: by weight by following original
Material composition: 34-39 parts of organosilicon modified crylic acid resin, 7-9 parts of expanded graphite, 12-15 parts of heat conducting fiber silk, mica powder 6-8
Part, 5-7 parts of compound transition metal oxide powder, 9-11 parts of butyl acetate, 0.5-1 parts of fumed silica, diacetone alcohol 12-
17 parts, 1-1.5 parts and levelling agent 0.5-1 parts of dispersing agent;Flexible heat-conductive coating can also be made of the raw material of following parts by weight: organic
39 parts of fluorine-silicon modified acrylic resin, 9 parts of expanded graphite, 15 parts of heat conducting fiber silk, 8 parts of mica powder, compound transition metal oxide
7 parts of powder, 11 parts of butyl acetate, 1 part of fumed silica, 17 parts of diacetone alcohol, 1.5 parts and 1 part of levelling agent of dispersing agent;As
It is preferred that flexible heat-conductive coating is made of following raw material by weight: 38 parts of organosilicon modified crylic acid resin, expanded graphite 8
Part, 14 parts of heat conducting fiber silk, 6 parts of mica powder, 6 parts of compound transition metal oxide powder, 10 parts of butyl acetate, gas phase titanium dioxide
0.7 part of silicon, 15 parts of diacetone alcohol, 1.3 parts and 0.7 part of levelling agent of dispersing agent.
Among the above, organosilicon modified crylic acid resin is copolymerized by vinylic organosiloxane monomer and acrylic ester monomer
It forms, with performances such as outstanding high temperature resistant, weatherability, good slightly flexible and strong adhesive force, this is used to lead as flexibility
The base-material of hot coating can make base-material have good thermally conductive, flexible and stability, and in the present embodiment, selection contains hydroxyl
Silicone modified acrylic resin, admittedly containing 50%, silicon contains 40%.
Expanded graphite, as thermally conductive reinforced filling, since it is with excellent thermal conductivity and flexibility, in the present embodiment
It is mainly used to, to form thermally conductive " terminal ", so that the heat in flexible heat-conductive coating is discharged rapidly as heat-conducting block, increase
The heat dissipation performance of strong flexibility heat-conductive coating.Preferably, expanded graphite select little particle expanded graphite, mesh number more than 325 mesh,
It is advisable below 400 mesh.
Heat conducting fiber silk, heat conducting fiber silk include metal fiber wire and carbon fiber wire, metal fiber wire and carbon fiber wire
Mass percent is 4:1, after two different kinds of heat conducting fiber silk is blended, can not only improve it is filametntary be uniformly distributed, also
It can be further formed the network thermal conducting path of three-dimensional shape, as shown in figure 3, being main channel with long and thin metal fiber filament 61, with carbon fiber
Tieing up silk 62 is tributary and overlap joint bridge, can be formed in coating continuous continual network-like " thermally conductive route ", coating by
When heating, heat can be scattered in coating everywhere by heat conducting fiber silk latticed in coating, and heat is all with coating after being dispersed
It encloses object and heat exchange occurs, and then reach heat dissipation purpose, the comprehensive of long and short fiber silk uses, and overcomes the fiber filament of single specification
Easily occur overlapping the problem of blind area and dispersion unevenness, solves network-like fiber and form the difficult and easy breakpoint of network-like fiber, do not connect
Continuous technological difficulties, meanwhile, the three-dimensional mesh fiber filament of formation additionally aids the increase of coating flexibility, make coating by
When stretching, compress, expanding with heat and contract with cold, the defects of being less prone to cracking, fold, crackle, compressed shape variability is extremely low, the base-material after solidification
It is not easily to fall off, stability enhancing.
In the present embodiment, metal fiber wire 61 can for brass fiber, stainless steel fibre, carbon steel fiber, aluminum fiber and
Aluminum alloy fiber is one such or several mixing, preferably the preferable brass fiber of heating conduction, more specifically, brass fiber
Filament diameter should be between 40-80 μm, with 50-60 μm for main filament diameter, draw ratio 40-60:1, to ensure brass fibre
Dimension silk has the performances such as thermally conductive, toughness good enough.Carbon fiber wire is thin short asphalt-based carbon fiber silk, and filament diameter is 10-15 μ
M, draw ratio 2-3:1, to ensure that carbon fiber wire can form good overlap joint bridge between brass fiber silk.
Mica powder can form substantially parallel orientations under the action of surface tension in coating, obstruct corrosivity
The infiltration to the flexible heat-conducting layer of formation such as substance such as water, machine oil, improves the corrosion resistance of coating, while mica powder can be with
Bear tensile stress, increase the adhesive force of coating, improve coating heat radiation and mechanical performance, the addition of mica powder, moreover it is possible to it is thermally conductive
Fiber acts synergistically, and reduces stress suffered by heat conducting fiber, the trend that heat conducting fiber is fallen off is reduced, in the present embodiment
In, sericite in powder is preferably used, first is that mica powder plays the best use.
Butyl acetate and diacetone alcohol are used as solvent in the present embodiment, can guarantee film-formation result when coating is dry,
Compared to single solvent, two kinds of solubility parameters are close, and the effect that can achieve mutual supplement with each other's advantages is blended with solvent similar in boiling point, gram
The intrinsic disadvantage of single solvent is taken, the film-formation result of coating is made to be easier to be protected, success rate is high.Fumed silica is at this
Anti-settling agent is used as in embodiment, fluffy powder shape, porous fumed silica can effectively improve the suspension of filler in coating,
The generation for preventing lamination makes coating keep good stability.Used in the process of dispersing agent is dispersed with stirring for reduction
Time enables mixture to be uniformly dispersed as early as possible, selects BYK-ATU dispersing agent in the present embodiment, levelling agent is for avoiding forming a film
There is phenomena such as shrinkage cavity, be a kind of polyacrylate solution, selects BYK-355 levelling agent.
Compound transition metal oxide powder 64 is used as heat-absorbing material in the present embodiment, and absorptance can reach 0.91,
Transmitting ratio is about 0.4, has very strong heat absorption capacity, after compound transition metal oxide powder 64 is evenly dispersed, in coating
Several heat sinks are formed, each heat sink is similar to " absorption heat pump ", the heat of surrounding is largely sucked, and then passes through thermally conductive fibre
It ties up silk and heat is transported in coating everywhere, make not will form amount of localized heat concentration phenomenon inside and outside coating, coating is heated evenly, heat absorption
Ability improves, so that coating stability is more preferable.As shown in figure 3, expanded graphite 63, compound transition metal oxide powder
64, three dimentional heat conduction network is collectively formed in metal fiber wire 61 and carbon fiber 62, in two-dimensional diagram, elongated metal fiber wire 61
It is overlapped to form basic rack, since, there are more overlap joint blind area, basic rack is more multibreak to possess between long and thin metal fiber filament 61
The basic rack of point, it is evenly dispersed at the overlap joint blind area of basic rack to have overlapped a thin short carbon fiber silks 62 several mutually, one
Point thin short carbon fiber silk 62 connects the basic rack of breakpoint, and most of breakpoint of basic rack is switched on, another part carefully short carbon
Fiber filament 62 and expanded graphite 63 and compound transition metal oxide powder 64 overlap, and pass through expanded graphite 63 and transition metal
Composite oxide power 64 connects basic rack indirectly, has generally formed uninterruptedly three dimentional heat conduction network.
Further, compound transition metal oxide can be FeMnCuO2、FeMnCuO3、FeMnCuO4、FeMnCuO5With
FeCuO5One such or several blendings, preferably FeCuO5。
Among the above, flexible heat-conductive coating preparation and application the following steps are included:
Organosilicon modified crylic acid resin and BYK-ATU dispersing agent are added in reactor step 1, then use blender
Mixed component is stirred up to being uniformly dispersed with the revolving speed of 800r/min, obtains base-material;
Step 2 sequentially adds asphalt-based carbon fiber silk, little particle expanded graphite, sericite into the base-material that step 1 obtains
Powder, fumed silica, FeCuO5Then powder is added butyl acetate and diacetone alcohol, is filled with blender to mixture
Divide stirring, mixing speed 1000r/min, until being uniformly dispersed, obtains initial point;
Brass fiber silk and BYK-355 levelling agent are added in the initial point of step 2 step 3, are dispersed with dispersion machine equal
Uncured coating is obtained after even, and uncured coating is pumped into the storage tank of air gun, is then sprayed with air gun
On processed substrate (in the present embodiment, substrate is mineral wool structure sheaf) surface, stands to coating levelling, be put into high temperature
Baking oven vacuum bakeout film-forming at 140 DEG C, then keeps the temperature 10min again, cools to the furnace after room temperature to obtain the final product.
Metallic reflective coating has biggish extinction coefficient, and reflectivity is very high, is a kind of outstanding light screening material, and metal is anti-
Film is penetrated for that in thermal insulation, sun-shade pad, can make thermal insulation, sun-shade pad that there is very high reflectivity, reflectivity is close to 1.Further, root
Difference is needed according to people, the metallic reflective coating of selection is also different, such as in the common metal thin material in ultra-violet (UV) band is aluminium, visible
The common metal thin material in light area is aluminium and silver, is gold, silver, copper metal thin material in infrared region common used material, in the present embodiment
In, consider to be used to reflected sunlight accident at metallic reflective coating, reflectance coating is also needed to have the function of weakening infrared energy, it is comprehensive
Consider, metallic reflective coating can select silver, aluminium, copper etc., preferably use silver metal thin material;Furthermore, metallic reflection is adopted
It is plated in tear resistant layer with the mode of sputter, (preferably 100 μm, also can choose 50 μm or 150 to sputter with a thickness of 50-150 μm
μm).
Fluorocarbon varnish has the characteristics that excellent weatherability, resistance to persistence, scratch resistance, flexibility, anti-corrosion and adhesive force are strong,
Make a kind of good cover protective coating, since fluorocarbon varnish is that clear dope will not when being coated on metallic reflective coating
Corrosion and destruction metallic reflective coating, while will not influence the reflectivity of metallic reflective coating, metallic reflective coating is protected well,
In the present embodiment, the coating thickness of fluorocarbon varnish is 150-300 μm (preferably 180 μm, also can choose 150 μm or 300 μm).
The setting of phase-change material 5 can play the role of auxiliary flexible heat-conducting layer heat radiator, be conducive to flexible heat-conducting layer and inhale
Hot radiation processes, by the function of phase-change material accumulation of heat, absorb soft when self-temperature is higher not in time for the heat dissipation of flexible heat-conducting layer
Property heat-conducting layer heat, reduce flexible heat-conducting layer temperature, and then play the heat radiator ability of flexible heat-conducting layer again, phase
When becoming material accumulation of heat to critical value, phase-change material no longer absorbs heat, and withdraws thermal insulation, sun-shade pad at this time, flexible heat-conducting layer is due to no longer inhaling
Hot temperature reduces rapidly, and phase-change material discharges accumulation of heat, and outwardly distributes heat by flexible heat-conducting layer, until restoring initial state
(solid-like) is realized and is recycled in case continuing to use next time.
In order to make phase-change material have above-mentioned function, phase-change material is solid-liquid phase change material, the phase of solid-liquid phase change material
Temperature is 31-36 DEG C, and furthermore, solid-liquid phase change material is made up of by mass percentage: expanded graphite 7%,
Binary eutectic fatty acid 87%, porous magnesia 2%, porous polyester fiber 2%, carboxymethyl cellulose 2%, wherein binary eutectic
Fatty acid is blended by lauric acid and myristic acid.Design binary eutectic fatty acid is phase-transition heat-storage matrix, due to laurel
Acid and myristic acid have it is cheap and easy to get, property stablize, it is almost non-toxic, it is environmentally friendly and renewable the features such as, binary eutectic fat
Acid is blended by lauric acid and myristic acid, and the phase transition temperature of the eutectic object formed after blending is suitable for meeting current demand (altogether
Phase transition temperature is at 20-50 DEG C after mixed), furtherly, in the present embodiment, it is desirable that obtained after lauric acid and myristic acid blending
Binary eutectic fatty acid phase transition temperature at 31-36 DEG C, latent heat of phase change 141-167J/g, phase transition temperature is selected in 31-
36 DEG C of cause is that the hot dynamic equilibrium temperature general control of body of a motor car and heat absorbing coating exists after mainly considering cooling
31-36 DEG C is more suitable for, it is preferable that by the control of hot dynamic equilibrium temperature at 33 DEG C, the influence of vehicle body temperature can be ignored not
Meter, geological measuring ratio corresponding to lauric acid and myristic acid is 58:42, phase transformation in the phase transition temperature of binary eutectic fatty acid at this time
Temperature is 33 DEG C or so, latent heat of phase change 151J/g.
Expanded graphite is common organic phase-change material, has a compatibility well with fatty acid organic matter, fatty acid/
In expanded graphite-based phase change composite material, the maximum adsorption quality of expanded graphite is up to 80%, and fatty acid is when undergoing phase transition, almost
Liquid leakage will not occur, there is very strong stability.But fatty acid/expanded graphite-based phase change composite material can only not by
To outstanding stability is just able to maintain in the case where greater impact power and bending power, when fatty acid/expanded graphite-based phase transformation is multiple
When condensation material is by greater impact power and bending power while folding (such as heat insulating mattress), in expanded graphite, the ground square hole that is stretched
Porosity can become larger, and easily be detached from for the fatty acid of liquid, can be become smaller by the local porosity compressed, be full of in gap
Interior liquid can be extruded and then lose adherence, and liquid flowing can occur for these liquid fatty acids for being detached from expanded graphite, into
And so that phase-change material layers is wrecked and ineffective, it therefore, in the present embodiment joined auxiliary shaping adsorbate porous oxidation
Magnesium and porous polyester fiber, porous magnesia have outstanding meso pore characteristics, and liquid fatty acid can sufficiently be adsorbed on porous oxygen
Change in magnesium matrix, after porous magnesia is mixed in binary eutectic fatty acid, when phase-change material layers are by impact force and bending power,
A large amount of porous magnesias are flooded in fatty acid to form liquid stream, the porous magnesia of these free shapes is that liquid stream fatty acid mentions
Point is adsorbed for mobile, and then increases the viscosity of liquid stream, prevents the trend of phase-change material layers malformation to a certain extent,
And then the problem of effectivelying prevent phase-change material laminar flow to leak, while in order to further be fully solved change material layer flowing leakage
Problem, also added porous polyester fiber in phase-change material layers, and porous polyester fiber not only can be with, moreover it is possible to amount of stored heat is improved,
Phase-change material layers are made to play optimum efficiency.
Porous magnesia and porous polyester fiber composite use, and in the phase-change material layers of formation, act synergistically, when
When solid fatty acid is undergone phase transition, free porous magnesia is mobile with liquid stream, porous polyester fiber will keep off obtain it is free
Porous magnesia further increases the viscosity of liquid stream, shows as on the whole, when phase-change material layers are undergone phase transition, the liquid of formation
Body is gathered in part since viscosity is big, not will form liquid stream, and then maintain the stable structure of phase-change material layers.Meanwhile phase
For change material layer when being stretched and impacting, the combined use of grain shape and fiber shape increases the tough of phase-change material layers
Property, tearing toughness and fatigue resistance, enable phase-change material layers to bend, improve its adaptability.
Furthermore, porous magnesia the preparation method comprises the following steps: weighing the triblock polymer F-127 template of design flow
Dehydrated alcohol and magnesium nitrate hexahydrate is added in reactor in agent, then is placed under vacuum environment and is stirred 10-15h, then will
Solution is put into drying in 50 DEG C of thermostatic drying chambers, is put into box resistance until sample is colloidal, then by obtained colloid
It is calcined in furnace in 450 DEG C, heating rate control is 2 DEG C/min, and 8h is calcined under air conditions, 2h is kept the temperature after calcining, so
After cool to room temperature with the furnace to obtain the final product.
The preparation method of above-mentioned solid-liquid phase change material the following steps are included:
Step 1, by under normality lauric acid and myristic acid be by mass percentage 58:42 ratio taken amount, then in
It is uniformly mixed in reactor, seals reactor and is kept the temperature in 80 DEG C of baking oven, until lauric acid and Pork and beans in reactor
Cool acid all melts, and then takes out and is uniformly mixed with blender, obtains binary eutectic fatty acid mixed solution;
Binary eutectic fatty acid mixed solution is placed in ultrasonic water bath pot by step 2, in 60 DEG C to binary eutectic rouge
Fat acid mixed solution carries out ultrasonic vibration 4min, be then again sealed off reactor be placed in 60 DEG C of baking oven keep the temperature it is spare;
Natural flake graphite is dried 12h in 50 DEG C of vacuum ovens by step 3, box in 800 DEG C with high temperature puffing method
It is heated in resistance furnace and expanded graphite is made, it is spare;
Expanded graphite obtained in step 3 is put into reactor by step 4, be put into reactor porous magnesia and
Porous polyester fiber, is then uniformly mixed, then 60 DEG C of water-bath heat preservations, spare;
Step 5, under vacuum conditions is instilled binary eutectic fatty acid mixed solution and carboxymethyl cellulose with dropper
In the reactor of step 4, until being added dropwise;
After the completion of step 6, step 5, reactor continues 60 DEG C of water-baths, with blender to being sufficiently stirred in reactor,
Until be uniformly mixed, then the material in reactor pours into the mold pre-processed to (in the present embodiment, mold is glass
Cotton structure layer), then mold is placed in freeze-day with constant temperature 20-30h in 70 DEG C of baking oven, finally take out and demould to obtain the final product.
To sum up, thermal insulation, sun-shade pad preparation method the following steps are included:
Step 1, braiding high-strength yarn, by 42-58 root aramid fiber and 21-29 root polyester fiber according to mass percent
Merge twisting into high-strength yarn for 2:1, high-strength yarn is then woven into tear resistant layer;
Obtained tear resistant layer is immersed in silica solution by step 2, is then allowed to stand carry out gel, is taken out after 10h and be put into 60
It is dried in DEG C thermostatic drying chamber, tear resistant layer after obtaining Gel Treatment (so that gel is full of the hole in tear resistant layer,
Intercept heat is propagated to vehicle body, greatly improves the heat-proof quality of tear resistant layer), it is spare;
Then step 3, the face jet-plating metallization reflectance coating in tear resistant layer spray fluorine carbon on the metallic reflective coating of formation
Varnish, it is spare after dry;
Mineral wool is pressed into mineral wool structure sheaf of the one side with cone substrate by step 4, manufacture mineral wool molding die,
It is spare;
Step 5, the face spray containment glue that cone substrate is had in mineral wool structure sheaf, and on the face of mineral wool structure sheaf
One layer of sealant is formed, it is spare after dry;
Step 6, manufacture solid-liquid phase change material, become liquid phase for solid-liquid phase change material heating and are placed on mineral wool structure sheaf
Cone substrate in, wherein bore intrabasement liquid phase phase-change material depth be no more than cone substrate height, then by glass cotton knot
Structure is placed on that vacuum tank is hollow to be cooled to room temperature;
Step 7 manufactures flexible heat-conductive coating, organosilicon modified crylic acid resin and dispersing agent is added in reactor, so
Mixed component is stirred up to being uniformly dispersed with the revolving speed of 800r/min with blender afterwards, base-material is obtained, then to base-material
In sequentially add carbon fiber wire, expanded graphite, mica powder, fumed silica, compound transition metal oxide powder, then plus
Enter butyl acetate and diacetone alcohol, mixture is sufficiently stirred with blender, mixing speed 1000r/min, until point
It dissipates uniformly, obtains initial point;
Metal fiber wire and levelling agent are added in the initial point of step 7 step 8, after being uniformly dispersed with dispersion machine
To uncured coating, uncured coating is pumped into the storage tank of air gun, is then sprayed on step 6 with air gun
Obtained mineral wool structure sheaf with cone substrate one side, coating thickness be 1-5mm(be preferably 2mm, also may be selected 1mm or
It 5mm) stands to coating levelling, is put into high temperature oven vacuum bakeout film-forming at 140 DEG C, then keeps the temperature 10min again, with
Furnace is cooled to room temperature, and obtains initial thermal insulation, sun-shade pad;
Step 9, tear resistant layer that step 3 obtains is obtained with step 7 without the one side of metallic reflective coating it is initial heat-insulated
Sun-shade cushion be adhesively fixed without the one side of flexible heat-conductive coating with binder after to get to thermal insulation, sun-shade pad.
As depicted in figs. 1 and 2, metallic reflective coating 2 reflects most sunlights, plays shaded effects well, remains
Remaining part divides sunlight and heat to be isolated by tear resistant layer 3, and heat and sunlight can not infiltrate into the rebasing portion of thermal insulation, sun-shade, in turn
Play heat insulation;When flexible heat-conducting layer 6 is contacted with vehicle body, it is a large amount of that the biggish temperature difference promotes flexible heat-conducting layer to absorb vehicle body
Heat, and then make the reduction of vehicle body constant temperature, until vehicle body and flexible heat-conducting layer 6 reach hot dynamic balancing, if heat dynamic is flat at this time
The temperature that weighs is higher, then phase-change material 5 largely absorbs the heat of flexible heat-conducting layer, promotes flexible 6 temperature of heat-conducting layer to reduce, and then make
Hot dynamic equilibrium temperature reduces, and on the whole, so that the temperature of vehicle body is in lower state, avoids the risk of scald.Meanwhile vehicle
The reduction of body temperature, it also occur that chain effect, further decreases interior temperature, it is 30 in temperature by on-the-spot test
DEG C open parking ground in, the thermal insulation, sun-shade pad of the present embodiment is covered after 1h on automobile, is measured with thermometer, interior temperature
Degree is differed with outside air temperature within 6 DEG C, and best only 2-3 DEG C of difference, the temperature of vehicle body is differed with outside air temperature within 9 DEG C,
Best only 4-5 DEG C of difference, hence it is evident that better than the existing thermal insulation, sun-shade pad used.
Embodiment two
Embodiment two is the same as example 1, the difference is that, solid-liquid phase change material is by mass percentage by following
Composition: expanded graphite 9%, binary eutectic fatty acid 82%, porous magnesia 1%, porous polyester fiber 5%, carboxymethyl cellulose
3%, wherein binary eutectic fatty acid is blended by lauric acid and myristic acid.
Embodiment three
Embodiment three is identical as embodiment one and embodiment two, the difference is that, solid-liquid phase change material presses quality hundred
Ratio is divided to be made up of: expanded graphite 7%, binary eutectic fatty acid 83%, porous magnesia 5%, porous polyester fiber 3%, carboxylic
Methylcellulose 2%, wherein binary eutectic fatty acid is blended by lauric acid and myristic acid.
The foregoing is merely illustrative of the preferred embodiments of the present invention, is not intended to limit the invention, all in essence of the invention
Made any modifications, equivalent replacements, and improvements etc., should all be included in the protection scope of the present invention within mind and principle.
Claims (3)
1. a kind of preparation method of automobile thermal insulation, sun-shade pad, which comprises the following steps:
Aramid fiber is merged twisting into height for 2:1 according to mass percent with polyester fiber by step 1, braiding high-strength yarn
Then high-strength yarn is woven into tear resistant layer by strength yarns;
Obtained tear resistant layer is immersed in silica solution by step 2, is then allowed to stand carry out gel, is taken out after 10h and be put into 60 DEG C of perseverances
It is dried in warm drying box, the tear resistant layer after obtaining Gel Treatment is spare;
Then it is clear to spray fluorine carbon on the metallic reflective coating of formation for step 3, the face jet-plating metallization reflectance coating in tear resistant layer
Paint, it is spare after dry;
Mineral wool is pressed into mineral wool structure sheaf of the one side with cone substrate by step 4, manufacture mineral wool molding die, spare;
Step 5 has a face spray containment glue of cone substrate in mineral wool structure sheaf, and is formed on the face of mineral wool structure sheaf
One layer of sealant, it is spare after dry;
Solid-liquid phase change material heating is become the cone that liquid phase is placed on mineral wool structure sheaf by step 6, manufacture solid-liquid phase change material
In substrate, wherein the depth for boring intrabasement liquid phase phase-change material is no more than the height of cone substrate, then by mineral wool structure sheaf
It is placed in that vacuum tank is hollow to be cooled to room temperature;
Step 7 manufactures flexible heat-conductive coating, and organosilicon modified crylic acid resin and dispersing agent are added in reactor, then used
Blender is stirred until be uniformly dispersed mixed component with the revolving speed of 800r/min, obtains base-material, then into base-material according to
Secondary addition carbon fiber wire, expanded graphite, mica powder, fumed silica, compound transition metal oxide powder, are then added vinegar
Acid butyl ester and diacetone alcohol are sufficiently stirred mixture with blender, mixing speed 1000r/min, until dispersion is equal
It is even, obtain initial point;
Metal fiber wire and levelling agent are added in the initial point of step 7 step 8, obtain not after being uniformly dispersed with dispersion machine
Uncured coating is pumped into the storage tank of air gun by cured coating, is then sprayed on step 6 with air gun and is obtained
One side of the mineral wool structure sheaf with cone substrate, stand to after coating levelling, be put into high temperature oven vacuum bakeout at 140 DEG C
Then film-forming keeps the temperature 10min again, cool to room temperature with the furnace, obtains initial thermal insulation, sun-shade pad;
Step 9, the initial thermal insulation, sun-shade for obtaining the tear resistant layer that step 3 obtains with step 7 without the one side of metallic reflective coating
It pads after the one side without flexible heat-conductive coating is adhesively fixed with binder to get to thermal insulation, sun-shade pad.
2. the preparation method of automobile thermal insulation, sun-shade pad as described in claim 1, which is characterized in that in step 1, aramid fiber is fine
It is 42-58 root that radical is measured by Wesy, and polyester fiber dosage radical is 21-29 root.
3. the preparation method of automobile thermal insulation, sun-shade pad as described in claim 1, which is characterized in that in step 6, solid-liquid
The phase transition temperature of phase-change material is 31-36 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201711301148.9A CN107972331B (en) | 2016-09-09 | 2016-09-09 | A kind of preparation method of automobile thermal insulation, sun-shade pad |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201711301148.9A CN107972331B (en) | 2016-09-09 | 2016-09-09 | A kind of preparation method of automobile thermal insulation, sun-shade pad |
CN201610814021.6A CN106240026B (en) | 2016-09-09 | 2016-09-09 | Automobile using thermal insulation, sun-shade pad |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610814021.6A Division CN106240026B (en) | 2016-09-09 | 2016-09-09 | Automobile using thermal insulation, sun-shade pad |
Publications (2)
Publication Number | Publication Date |
---|---|
CN107972331A CN107972331A (en) | 2018-05-01 |
CN107972331B true CN107972331B (en) | 2019-07-30 |
Family
ID=57599532
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201711301148.9A Expired - Fee Related CN107972331B (en) | 2016-09-09 | 2016-09-09 | A kind of preparation method of automobile thermal insulation, sun-shade pad |
CN201610814021.6A Expired - Fee Related CN106240026B (en) | 2016-09-09 | 2016-09-09 | Automobile using thermal insulation, sun-shade pad |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610814021.6A Expired - Fee Related CN106240026B (en) | 2016-09-09 | 2016-09-09 | Automobile using thermal insulation, sun-shade pad |
Country Status (1)
Country | Link |
---|---|
CN (2) | CN107972331B (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110499649A (en) * | 2018-05-18 | 2019-11-26 | 澳洋集团有限公司 | A kind of preparation method of heat-resistant fabric |
CN109177419A (en) * | 2018-10-11 | 2019-01-11 | 泉州市联控自动化科技有限公司 | A kind of sun-proof Sunshade film of phase transformation |
CN113500833B (en) * | 2021-05-19 | 2023-06-09 | 深圳市华科创智技术有限公司 | Flexible phase-change automatic temperature control device for intelligent wearing and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN203888586U (en) * | 2014-06-26 | 2014-10-22 | 张天华 | Inflatable sunshade pad in automobile |
CN104943511A (en) * | 2015-07-10 | 2015-09-30 | 江苏领腾汽车部件有限公司 | Durable heat-insulating and sun-shading automotive pad |
CN204820516U (en) * | 2015-07-10 | 2015-12-02 | 江苏领腾汽车部件有限公司 | Car sunshade pad that insulates against heat |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10033322B4 (en) * | 2000-07-03 | 2005-08-04 | HP-chemie Pelzer Ltd. Industrial Estate | Method for producing composite elements and composite element |
KR100830060B1 (en) * | 2006-12-15 | 2008-05-19 | 한국과학기술연구원 | Phase-change ram and fabrication method thereof |
CN202200918U (en) * | 2011-06-22 | 2012-04-25 | 中国科学院深圳先进技术研究院 | Automobile |
CN203088633U (en) * | 2012-11-20 | 2013-07-31 | 浙江三赢医疗器械有限公司 | Gel cushion containing phase-change material |
CN206217262U (en) * | 2016-09-09 | 2017-06-06 | 泰安天元棉麻有限公司 | Automobile thermal insulation, sun-shade pad |
-
2016
- 2016-09-09 CN CN201711301148.9A patent/CN107972331B/en not_active Expired - Fee Related
- 2016-09-09 CN CN201610814021.6A patent/CN106240026B/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN203888586U (en) * | 2014-06-26 | 2014-10-22 | 张天华 | Inflatable sunshade pad in automobile |
CN104943511A (en) * | 2015-07-10 | 2015-09-30 | 江苏领腾汽车部件有限公司 | Durable heat-insulating and sun-shading automotive pad |
CN204820516U (en) * | 2015-07-10 | 2015-12-02 | 江苏领腾汽车部件有限公司 | Car sunshade pad that insulates against heat |
Also Published As
Publication number | Publication date |
---|---|
CN106240026B (en) | 2018-05-11 |
CN106240026A (en) | 2016-12-21 |
CN107972331A (en) | 2018-05-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107972331B (en) | A kind of preparation method of automobile thermal insulation, sun-shade pad | |
Li et al. | All-Ceramic, compressible and scalable nanofibrous aerogels for subambient daytime radiative cooling | |
CN105860717B (en) | Colour reflective insulating moulding coating and its preparation, construction method | |
CN104559398A (en) | Manufacturing method of high-performance heat insulation material | |
WO2021035816A1 (en) | Two-component thermal storage potting material and preparation method therefor | |
CN101824258A (en) | Waterborne reflective heat-insulating building coating | |
CN101561194A (en) | Solar energy heat collector | |
Li et al. | Recent progress in organic-based radiative cooling materials: fabrication methods and thermal management properties | |
CN112721375A (en) | Radiation refrigeration composite fabric, preparation method and device | |
CN101205435A (en) | Solar heat reflective insulation paint and preparation thereof | |
CN110815978A (en) | Heat insulation cloth and preparation method thereof | |
CN106398433B (en) | A kind of flexible heat-conductive coating for automobile heat insulation | |
Chen et al. | Eco‐Friendly Transparent Silk Fibroin Radiative Cooling Film for Thermal Management of Optoelectronics | |
CN206217262U (en) | Automobile thermal insulation, sun-shade pad | |
Wang et al. | Bioinspired multilayer structures for energy-free passive heating and thermal regulation in cold environments | |
KR101655558B1 (en) | Temperature-sensitive color change complex pigment with core-shell structure, method for manufacturing the same and smart color changing paint composition using the same | |
Huo et al. | Expanded graphite@ octadecanol composite phase change material with photothermal conversion interface | |
Feng et al. | Integrated passive cooling fabrics with bioinspired perspiration-wicking for outdoor personal thermal management | |
Feng et al. | Dual-asymmetrically selective interfaces-enhanced poly (lactic acid)-based nanofabric with sweat management and switchable radiative cooling and thermal insulation | |
Tao et al. | Incorporation form-stable phase change material with passive radiative cooling emitter for thermal regulation | |
Zhang et al. | Colourful phase change material-incorporated flexible film for efficient passive radiative cooling | |
Tu et al. | Hierarchically structured composite with superhydrophobicity and radiative cooling for energy-saving buildings | |
Chai et al. | Composite Phase-Change Materials for Photo-Thermal Conversion and Energy Storage: A review | |
CN114368211A (en) | Heat insulation sunshade pad for automobile | |
CN114892417B (en) | Textile containing daytime radiation refrigeration porous coating, and preparation method and application thereof |
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 | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20190730 |