CN113789043A - Heat-conducting junction box material and preparation method and application thereof - Google Patents
Heat-conducting junction box material and preparation method and application thereof Download PDFInfo
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- CN113789043A CN113789043A CN202111153954.2A CN202111153954A CN113789043A CN 113789043 A CN113789043 A CN 113789043A CN 202111153954 A CN202111153954 A CN 202111153954A CN 113789043 A CN113789043 A CN 113789043A
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- 239000000463 material Substances 0.000 title claims abstract description 84
- 238000002360 preparation method Methods 0.000 title claims abstract description 18
- 239000000956 alloy Substances 0.000 claims abstract description 38
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 36
- 229920005989 resin Polymers 0.000 claims abstract description 31
- 239000011347 resin Substances 0.000 claims abstract description 31
- 239000000203 mixture Substances 0.000 claims abstract description 23
- 239000004594 Masterbatch (MB) Substances 0.000 claims abstract description 19
- 239000011159 matrix material Substances 0.000 claims abstract description 16
- 239000000945 filler Substances 0.000 claims abstract description 12
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 8
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 8
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 23
- 229920001400 block copolymer Polymers 0.000 claims description 18
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 claims description 18
- -1 3, 5-di-tert-butyl-4-hydroxyphenyl Chemical group 0.000 claims description 16
- 239000011231 conductive filler Substances 0.000 claims description 13
- 239000006229 carbon black Substances 0.000 claims description 11
- 238000001035 drying Methods 0.000 claims description 10
- 238000001125 extrusion Methods 0.000 claims description 10
- 238000005469 granulation Methods 0.000 claims description 10
- 230000003179 granulation Effects 0.000 claims description 10
- 239000004793 Polystyrene Substances 0.000 claims description 9
- 239000002131 composite material Substances 0.000 claims description 9
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052582 BN Inorganic materials 0.000 claims description 7
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 7
- 229910007948 ZrB2 Inorganic materials 0.000 claims description 7
- VWZIXVXBCBBRGP-UHFFFAOYSA-N boron;zirconium Chemical compound B#[Zr]#B VWZIXVXBCBBRGP-UHFFFAOYSA-N 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 7
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 7
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 6
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 6
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 6
- 239000000919 ceramic Substances 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 6
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 5
- 239000004917 carbon fiber Substances 0.000 claims description 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- 239000007977 PBT buffer Substances 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 claims description 4
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- SBKRBXBQFDKYSO-UHFFFAOYSA-N (3-tert-butyl-4-hydroxy-5-methylphenyl) propanoate Chemical compound CCC(=O)OC1=CC(C)=C(O)C(C(C)(C)C)=C1 SBKRBXBQFDKYSO-UHFFFAOYSA-N 0.000 claims description 2
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 claims description 2
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229920002943 EPDM rubber Polymers 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- BFDAIBXRNHJYJM-UHFFFAOYSA-N OP(O)OP(O)O.C(C)(C)(C)C=1C=C(C=C(C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=CC(=CC(=C1)C(C)(C)C)C(C)(C)C Chemical compound OP(O)OP(O)O.C(C)(C)(C)C=1C=C(C=C(C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=CC(=CC(=C1)C(C)(C)C)C(C)(C)C BFDAIBXRNHJYJM-UHFFFAOYSA-N 0.000 claims description 2
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 claims description 2
- 229910026551 ZrC Inorganic materials 0.000 claims description 2
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 claims description 2
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 claims description 2
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000292 calcium oxide Substances 0.000 claims description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 2
- 229910002804 graphite Inorganic materials 0.000 claims description 2
- 239000010439 graphite Substances 0.000 claims description 2
- 229920005669 high impact polystyrene Polymers 0.000 claims description 2
- 239000004797 high-impact polystyrene Substances 0.000 claims description 2
- 239000000395 magnesium oxide Substances 0.000 claims description 2
- 229910000480 nickel oxide Inorganic materials 0.000 claims description 2
- YPNZYYWORCABPU-UHFFFAOYSA-N oxiran-2-ylmethyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CC(=C)C(=O)OCC1CO1 YPNZYYWORCABPU-UHFFFAOYSA-N 0.000 claims description 2
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 claims description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000011787 zinc oxide Substances 0.000 claims description 2
- XCPFSALHURPPJE-UHFFFAOYSA-N (3,5-ditert-butyl-4-hydroxyphenyl) propanoate Chemical compound CCC(=O)OC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 XCPFSALHURPPJE-UHFFFAOYSA-N 0.000 claims 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical group OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
- 229920001955 polyphenylene ether Polymers 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 65
- 229920006380 polyphenylene oxide Polymers 0.000 description 65
- 230000000052 comparative effect Effects 0.000 description 21
- 239000012467 final product Substances 0.000 description 8
- BOFDULGALQZOGC-UHFFFAOYSA-N C(CC)(=O)O.C(C)(C)(C)C=1C=C(C=C(C1O)C(C)(C)C)C(O)C(CO)(CO)CO Chemical compound C(CC)(=O)O.C(C)(C)(C)C=1C=C(C=C(C1O)C(C)(C)C)C(O)C(CO)(CO)CO BOFDULGALQZOGC-UHFFFAOYSA-N 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 5
- 239000004417 polycarbonate Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000012994 photoredox catalyst Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 239000012745 toughening agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- XYXJKPCGSGVSBO-UHFFFAOYSA-N 1,3,5-tris[(4-tert-butyl-3-hydroxy-2,6-dimethylphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C)=C1CN1C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C1=O XYXJKPCGSGVSBO-UHFFFAOYSA-N 0.000 description 1
- 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
- DXCHWXWXYPEZKM-UHFFFAOYSA-N 2,4-ditert-butyl-6-[1-(3,5-ditert-butyl-2-hydroxyphenyl)ethyl]phenol Chemical compound C=1C(C(C)(C)C)=CC(C(C)(C)C)=C(O)C=1C(C)C1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1O DXCHWXWXYPEZKM-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229910001125 Pa alloy Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
- C08L71/12—Polyphenylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02G—INSTALLATION OF ELECTRIC CABLES OR LINES, OR OF COMBINED OPTICAL AND ELECTRIC CABLES OR LINES
- H02G3/00—Installations of electric cables or lines or protective tubing therefor in or on buildings, equivalent structures or vehicles
- H02G3/02—Details
- H02G3/08—Distribution boxes; Connection or junction boxes
-
- 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
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- 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
- C08K3/28—Nitrogen-containing compounds
- C08K2003/282—Binary compounds of nitrogen with aluminium
-
- 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
- C08K3/38—Boron-containing compounds
- C08K2003/382—Boron-containing compounds and nitrogen
- C08K2003/385—Binary compounds of nitrogen with boron
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a heat-conducting junction box material and a preparation method and application thereof. The heat-conducting junction box material comprises the following components in percentage by weight: 50-80% of matrix resin, 20-50% of heat-conducting filler, 0-6% of compatilizer, 0.2-1.5% of antioxidant and 1-5% of black master batch, wherein the matrix resin is an alloy formed by any one or a mixture of at least two of PPO, PC, PP, PA, PS, PE, PBT or ABS. The heat-conducting junction box material disclosed by the invention has the advantages that the heat-conducting property and the electric conductivity are improved, and meanwhile, the mechanical property of the material is ensured, so that the material is particularly suitable for preparing the heat-conducting junction box.
Description
Technical Field
The invention relates to the technical field of junction box materials, relates to a junction box material and a preparation method and application thereof, and particularly relates to a heat-conducting junction box material and a preparation method and application thereof.
Background
At present, most of the materials of the junction boxes used in the market are polyphenylene oxide (PPO) materials or modified alloy materials thereof. The PPO material has good mechanical property, creep resistance, water resistance, high temperature resistance and other properties, and is widely applied to the fields of electronic appliances and the like due to the excellent properties of the PPO material. The heat-conducting property of the existing product in actual use can not completely meet the use requirement, so a material with high heat-conducting property is developed.
CN102977603A discloses a high-temperature-resistant high-thermal-conductivity PPS/PPO alloy and a preparation method thereof, belonging to the technical field of high polymer materials. The PPS/PPO alloy consists of the following raw materials in percentage by weight: PPS 20-50%, PPO 8-10%, toughening compatilizer 5-8%, heat conducting agent 5-48%, carbon fiber 20-30%, antioxidant 0.2-0.5% and processing aid 0.8-1.5%. The high-temperature-resistant high-thermal-conductivity PPS/PPO alloy disclosed by the invention has the characteristics of high thermal conductivity, high strength, high impact, good processability and the like.
CN103436000A discloses a heat-conducting reinforced PPO/PA alloy and a preparation method thereof, belonging to the technical field of high polymer materials. The alloy comprises the following raw materials in parts by weight: 60-90 parts of polyphenyl ether, 50-80 parts of nylon, 2-4 parts of silicon carbide whiskers, 6-8 parts of carbon fibers, 12-16 parts of silicon micropowder, 2-5 parts of nano aluminum oxide, 10-20 parts of melamine pyrophosphate, 0.5-1 part of antioxidant, 0.5-1 part of lubricant TAF, 7-11 parts of toughening agent and 1-3 parts of maleic anhydride grafted ethylene-1-octene copolymer. The product prepared by the invention has good mechanical property, high stability, good flame retardant property and heat conductivity, and the alloy can replace part of metal raw materials to produce parts and shells.
The alloy material of the above patent adds carbon fiber as heat conductive material, and although the heat conductive property is improved and the electric conductivity of the material is also improved, the mechanical property of the material is also reduced, which limits the application of the material.
CN103289367A discloses a high-temperature-resistant heat-conducting PA/PPO/PP composite material, which is composed of the following components in parts by weight: PA15-30 parts, PPO45-70 parts, PP20-35 parts, anti-aging agent 2-8 parts, plasticizer 3-8 parts, titanium dioxide 6-10 parts, calcium carbonate 2-6 parts, dibutyltin maleate 3-7 parts and toughening agent 3-8 parts. Titanium dioxide and calcium carbonate are added into the composite material, but the two fillers have low self-thermal conductivity and low filling amount, so that the thermal conductivity of the material cannot be well improved when the filler is filled into the material.
Disclosure of Invention
Aiming at the defects of the prior art, the invention aims to provide a heat-conducting junction box material and a preparation method and application thereof.
One of the objectives of the present invention is to provide a heat conductive junction box material, and to achieve the objective, the present invention adopts the following technical scheme:
a heat-conducting junction box material comprises the following components in percentage by weight:
wherein the matrix resin is an alloy formed by any one or a mixture of at least two of PPO, PC, PP, PE, PA, PS, PBT or ABS.
The heat-conducting junction box material takes the alloy formed by any one or at least two mixtures of PPO, PC, PP, PA, PS, PBT or ABS as matrix resin, and the mechanical property of the material is ensured while the heat-conducting property and the electric conductivity are improved by adding the heat-conducting filler.
Specifically, the heat-conducting junction box material comprises the following components in percentage by weight:
the weight percentage of the matrix resin is 50-80%, for example, 50%, 55%, 60%, 65%, 70%, 75%, or 80%.
The weight percentage of the heat conductive filler is 20-50%, for example, 20%, 25%, 30%, 35%, 40%, 45%, 50%, or the like.
The weight percent of the compatibilizer is 0-6%, such as 1%, 2%, 3%, 4%, 5%, or 6%, and the like.
The antioxidant is 0.2 to 1.5% by weight, for example, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1%, 1.1%, 1.2%, 1.3%, 1.4%, or 1.5%.
The weight percentage of the black master batch is 1-5%, for example, 1%, 2%, 3%, 4%, or 5%.
In the invention, the matrix resin is preferably PPO or PPO alloy.
In the invention, the PPO alloy is an alloy formed by PPO and any one or at least two of PS, PA, PPS, PBT and PP.
In the invention, the mass content of the PPO in the PPO alloy is 60-80%, for example, the mass content of the PPO is 60%, 65%, 70%, 75% or 80%. This is because the PPO material itself has excellent dielectric properties, water resistance, dimensional stability and the like, but also has problems of stress cracking, difficulty in processing and the like. So that the material is modified to have higher PPO content and better heat resistance.
In the invention, the PS is HIPS.
In the invention, the PA is any one or a mixture of at least two of PA6, PA66 and PA 12.
In the invention, the heat-conducting filler is any one or a mixture of at least two of aluminum oxide, magnesium oxide, zinc oxide, calcium oxide, nickel oxide, aluminum nitride, boron nitride, silicon carbide, beryllium oxide, zirconium diboride, zirconium carbide, high-heat-conductivity composite ceramic powder, carbon fiber, carbon black and graphite. Many fillers improve the thermal conductivity and the electrical conductivity of the material, but the addition of the fillers can reduce the mechanical properties of the material. The addition of the heat-conducting filler greatly improves the heat-conducting property of the material, and simultaneously also considers other properties of the material.
The compatilizer is any one or a mixture of at least two of N, N, N, N, -tetraglycidyl-4, 4-diaminobenzene methane, citric acid, styrene grafted maleic anhydride, polyphenyl ether grafted maleic anhydride, styrene-glycidyl methacrylate, styrene-butadiene-styrene block copolymer, styrene-ethylene-butadiene-styrene block copolymer, ethylene propylene diene monomer, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and acrylonitrile-butadiene-styrene copolymer grafted maleic anhydride.
The antioxidant is beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester, beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid octadecyl ester, N-bis [ beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionyl ] -1, 6-ethylenediamine, N-bis [ beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionyl ] hydrazine, 1,3, 5-tris (4-tert-butyl-3-hydroxy-2, 6-dimethylbenzyl) 1,3, 5-triazine-2, 4,6- (1H,3H,5H) -trione, triethylene glycol ether-bis (3-tert-butyl-4-hydroxy-5-methylphenyl) propionate, Any one or a mixture of at least two of 2, 2-ethylene-bis (4, 6-di-tert-butylphenol), tris (2, 4-di-tert-butylphenol) phosphite, dioctadecyl alcohol pentaerythritol diphosphite, bis (3, 5-di-tert-butylphenyl) pentaerythritol diphosphite and 3, 3-thiopropionic acid stearyl ester.
In the invention, the black master batch is a mixture of toner and matrix resin.
Preferably, the black master batch is a mixture of toner and matrix resin, wherein the matrix resin is an alloy formed by any one or at least two of PPO, PC, PP, PE, PA, PS, PBT or ABS.
Preferably, the mass ratio of the toner to the matrix resin is (20-40) to (60-80).
Preferably, the toner is carbon black.
The second purpose of the invention is to provide a preparation method of the heat-conducting junction box material, which comprises the following steps: and stirring and mixing the matrix resin, the heat-conducting filler, the compatilizer and the antioxidant according to the proportion, and performing extrusion granulation and drying to obtain the heat-conducting junction box material.
The invention also aims to provide application of the heat-conducting junction box material, and the heat-conducting junction box material is used for preparing a heat-conducting junction box.
Compared with the prior art, the invention has the beneficial effects that:
the heat-conducting junction box material disclosed by the invention has the advantages that the heat-conducting property and the electric conductivity are improved, and meanwhile, the mechanical property of the material is ensured. Specifically, the thermal conductivity coefficient of the thermal conductive junction box material prepared by the invention is 0.37-0.67W/DEG C.m, and the bulk resistance is 4.9 multiplied by 1015-8.9×1015Tensile strength of 31.7-75MPa and impact strength of 2.9-7.2KJ/m2。
Detailed Description
The technical solution of the present invention is further explained by the following embodiments.
Unless otherwise specified, various starting materials of the present invention are commercially available or prepared according to conventional methods in the art.
Example 1
The heat-conducting junction box material comprises the following components in percentage by weight: 72% of PPO resin, 15% of aluminum nitride, 5% of zirconium diboride, 4.5% of styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester and 3% of black master batch, wherein the black master batch is a mixture of carbon black and PPO resin in a mass ratio of 20: 80.
The preparation method of the heat-conducting junction box material comprises the following steps: PPO, aluminum nitride, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester are mixed uniformly by a high-speed mixer according to the proportion, and after extrusion granulation, the temperature of each section of the extruder is as follows: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Example 2
The heat-conducting junction box material comprises the following components in percentage by weight: 67% of PPO resin, 20% of boron nitride, 5% of zirconium diboride, 4.5% of styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester and 3% of black master batch, wherein the black master batch is a mixture of carbon black and PPO resin in a mass ratio of 20: 80.
The preparation method of the heat-conducting junction box material comprises the following steps: PPO, boron nitride, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester are mixed uniformly by a high-speed mixer according to the proportion, and after extrusion granulation, the temperature of each section of the extruder is as follows: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Example 3
The heat-conducting junction box material comprises the following components in percentage by weight: 57% of PPO resin, 30% of silicon carbide, 5% of high-thermal-conductivity composite ceramic powder, 4.5% of styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate pentaerythritol ester and 3% of black master batch, wherein the black master batch is a mixture of carbon black and PPO resin in a mass ratio of 20: 80.
The preparation method of the heat-conducting junction box material comprises the following steps: PPO, silicon carbide, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester are mixed uniformly by a high-speed mixer according to the proportion, and after extrusion granulation, the temperature of each section of the extruder is as follows: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Example 4
The heat-conducting junction box material comprises the following components in percentage by weight: 47% of PPO resin, 35% of aluminum oxide, 10% of zirconium diboride, 4.5% of styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester and 3% of black master batch, wherein the black master batch is a mixture of carbon black and PPO resin in a mass ratio of 20: 80.
The preparation method of the heat-conducting junction box material comprises the following steps: PPO, alumina, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester are mixed uniformly by a high-speed mixer according to the proportion, and after extrusion granulation, the temperature of each section of the extruder is as follows: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Example 5
The heat-conducting junction box material comprises the following components in percentage by weight: 47% of PPO resin, 45% of a mixture of aluminum oxide, zirconium diboride and boron nitride (the mass ratio is 4:2:3), 4.5% of styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) pentaerythritol propionate and 3% of black master batch, wherein the black master batch is a mixture of carbon black and PPO resin with the mass ratio of 20: 80.
The preparation method of the heat-conducting junction box material comprises the following steps: PPO, alumina, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester are mixed uniformly by a high-speed mixer according to the proportion, and after extrusion granulation, the temperature of each section of the extruder is as follows: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Example 6
The heat-conducting junction box material comprises the following components in percentage by weight: 47% of PPO alloy resin (wherein the mass ratio of PPO to PA is 7:3), 20% of aluminum oxide, 10% of boron nitride, 8% of zirconium diboride, 7% of high-thermal-conductivity composite ceramic powder, 4.5% of styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester and 3% of black master batch, wherein the black master batch is a mixture of carbon black and the PPO alloy resin in a mass ratio of 20: 80.
The preparation method of the heat-conducting junction box material comprises the following steps: PPO, PA, silicon carbide, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and beta (3, 5-di-tert-butyl-4-hydroxyphenyl) pentaerythritol propionate are mixed uniformly by a high-speed mixer according to the proportion, and after extrusion granulation, the temperature of each section of the extruder is as follows: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Example 7
The heat-conducting junction box material comprises the following components in percentage by weight: 47% of PPO alloy resin (wherein the mass ratio of PPO to PS is 7:3), 35% of silicon carbide, 10% of high-thermal-conductivity composite ceramic powder, 4.5% of styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) pentaerythritol propionate and 3% of black master batch, wherein the black master batch is a mixture of carbon black and the PPO alloy resin in a mass ratio of 20: 80.
The preparation method of the heat-conducting junction box material comprises the following steps: PPO, PA, silicon carbide, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride and beta (3, 5-di-tert-butyl-4-hydroxyphenyl) pentaerythritol propionate are mixed uniformly by a high-speed mixer according to the proportion, and after extrusion granulation, the temperature of each section of the extruder is as follows: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Example 8
This example is different from example 6 in that the PPO alloy has a PPO content of 40% by weight, and the other examples are the same as those of example 6.
Example 9
This example is different from example 6 in that the PPO alloy has 90% by weight of PPO, and the other examples are the same as those of example 6.
Example 10
This example differs from example 6 in that the PPO alloy was replaced with polycarbonate, and the rest was the same as example 6.
Example 11
This example is different from example 2 in that the heat conductive filler, boron nitride, was replaced with silica, and the others were the same as those of example 2.
Comparative example 1
The preparation method of the heat-conducting junction box material of the comparative example comprises the following steps: uniformly mixing 99.5% of PPO and 0.5% of beta (3, 5-di-tert-butyl-4-hydroxyphenyl) pentaerythritol propionate by a high-speed mixer, and performing extrusion granulation at the temperature of each section of the extruder: drying at 150 deg.C in the first region, 220 deg.C in the second region, 250 deg.C in the third region, 255 deg.C in the fourth region, 260 deg.C in the fifth region, 265 deg.C in the sixth region, 270 deg.C in the seventh region, 275 deg.C in the eighth region, 275 deg.C in the ninth region and 275 deg.C in the tenth region, to obtain the final product.
Comparative example 2
This comparative example differs from example 6 in that the amount of PPO alloy was 40% and the amount of reduced PPO alloy was increased on average to the other components to ensure that the total amount remained the same, all other things being equal to example 6.
Comparative example 3
This comparative example differs from example 6 in that the PPO alloy is used in an amount of 95% and the amount of PPO alloy added is on average subtracted from the other components to ensure that the total amount remains the same, all other things being equal to example 6.
Comparative example 4
This comparative example differs from example 6 in that the amount of the heat conductive filler was 1%, and the amount of the reduced heat conductive filler alloy was added on average to the other components to ensure that the total amount was constant, which were otherwise the same as those of example 6.
Comparative example 5
This comparative example is different from example 2 in that the amount of the heat conductive filler was 60%, and the amount of the heat conductive filler added was subtracted from the other components on average to ensure that the total amount was constant, which was otherwise the same as example 2.
Comparative example 6
This comparative example differs from example 2 in that the amount of the reduced heat conductive filler alloy was added on average to the other components to ensure that the total amount was constant, without adding the heat conductive filler, and the others were the same as in example 2.
Wherein, the PPO powder (the melt index is 4-40g/10min) manufacturers adopted in the above examples and comparative examples are Sabik in America, the high thermal conductivity composite ceramic powder manufacturers are Shanghai Shenyi New Material science and technology Co., Ltd, the junction box materials prepared in examples 1-11 and comparative examples 1-6 are subjected to performance tests, and the test results are shown in Table 1.
Wherein the test standard for thermal conductivity is performed in accordance with ASTM D5470; the test standard of the volume resistivity is carried out according to the GB/T1410-2006 standard; the test standard for tensile properties is carried out with reference to GB/T1040; the test standard for impact properties is carried out with reference to ISO 179.
TABLE 1
As can be seen from table 1, the thermally conductive junction box materials of examples 1 to 7 have good thermal conductivity and mechanical properties while maintaining good insulation properties. As the content of the heat-conducting filler is gradually increased, the heat conductivity coefficient of the PPO material is gradually increased, and the mechanical property is reduced. Compared with comparative example 1, the heat conductivity coefficient of all PPO materials added with the heat-conducting filler is improved.
Examples 6 and 7 show a better improvement in the processability of the material compared with example 5.
Too little weight percentage of the PPO alloy in example 8 results in a reduction of the mechanical properties of the material produced.
Too much weight percent of the PPO alloy in example 9 makes the forming of the resulting material difficult.
In the embodiment 10, the PPO alloy is replaced by PC resin, so that the mechanical property of the prepared material is reduced, and meanwhile, the mechanical property of the prepared composite material is reduced to a large extent by adding the inorganic filler.
The replacement of the thermally conductive filler in example 11 with silica did not significantly improve the thermal conductivity of the resulting material.
The pure PPO in the comparative example 1 has good mechanical property, but the heat conductivity is not high, so the pure PPO needs to be modified to improve the heat conductivity of the material.
Too little PPO alloy in comparative example 2 resulted in a reduction in the mechanical properties of the material produced.
Too much PPO alloy in comparative example 3 resulted in insufficient thermal conductivity of the resulting material.
The amount of the thermally conductive filler in comparative example 4 is too small, which results in a material having low thermal conductivity and is insufficient for improving the thermal conductivity of the material.
The comparative example 5, in which the amount of the heat conductive filler was too large, resulted in a better improvement in the heat conductive properties of the resulting material, but the material was severely deteriorated in mechanical properties due to the excessive addition of the inorganic substance.
The comparative example 6, in which no heat conductive filler is added, makes the obtained material have better mechanical properties and processability, but the application field of the material is limited due to poor heat conductive property in practical application.
The present invention is illustrated by the above-mentioned examples, but the present invention is not limited to the above-mentioned detailed process equipment and process flow, i.e. it is not meant to imply that the present invention must rely on the above-mentioned detailed process equipment and process flow to be practiced. It should be understood by those skilled in the art that any modification of the present invention, equivalent substitutions of the raw materials of the product of the present invention, addition of auxiliary components, selection of specific modes, etc., are within the scope and disclosure of the present invention.
The preferred embodiments of the present invention have been described in detail, however, the present invention is not limited to the specific details of the above embodiments, and various simple modifications may be made to the technical solution of the present invention within the technical idea of the present invention, and these simple modifications are within the protective scope of the present invention.
It should be noted that the various technical features described in the above embodiments can be combined in any suitable manner without contradiction, and the invention is not described in any way for the possible combinations in order to avoid unnecessary repetition.
In addition, any combination of the various embodiments of the present invention is also possible, and the same should be considered as the disclosure of the present invention as long as it does not depart from the spirit of the present invention.
Claims (10)
2. The thermally conductive junction box material of claim 1, wherein the matrix resin is PPO or PPO alloy;
preferably, the PPO alloy is an alloy of PPO with any one or at least two of PS, PA, PPS, PBT and PP.
3. The material of claim 1 or 2, wherein the mass content of the PPO in the PPO alloy is 60-80%.
4. The thermally conductive junction box material of claim 2, wherein the PS is HIPS.
5. The thermally conductive junction box material of claim 2, wherein the PA is any one of PA6, PA66, and PA12 or a mixture of at least two thereof.
6. The material of any one of claims 1 to 5, wherein the thermally conductive filler is any one or a mixture of at least two of alumina, magnesia, zinc oxide, calcium oxide, nickel oxide, aluminum nitride, boron nitride, silicon carbide, beryllium oxide, carbon fiber, zirconium diboride, zirconium carbide, high thermal conductivity composite ceramic powder, carbon black, and graphite.
7. The thermally conductive junction box material of any one of claims 1-6 wherein the compatibilizer is any one or a mixture of at least two of N, N, N, N, -tetraglycidyl-4, 4-diaminodiphenylmethane, citric acid, styrene grafted maleic anhydride, polyphenylene ether grafted maleic anhydride, styrene-glycidyl methacrylate, styrene-butadiene-styrene block copolymer, styrene-ethylene-butadiene-styrene block copolymer, ethylene propylene diene monomer, styrene-ethylene-butadiene-styrene block copolymer grafted maleic anhydride, and acrylonitrile-butadiene-styrene copolymer grafted maleic anhydride.
8. The thermally conductive junction box material of any one of claims 1 to 7 wherein the antioxidant is pentaerythritol beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate, octadecyl beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate, N-bis [ beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionyl ] -1, 6-ethylenediamine, N-bis [ beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionyl ] hydrazine, 1,3, 5-tris (4-tert-butyl-3-hydroxy-2, 6-dimethylbenzyl) 1,3, 5-triazine-2, 4,6- (1H,3H,5H) -any one or a mixture of at least two of triketone, triethylene glycol ether-bis (3-tert-butyl-4-hydroxy-5-methylphenyl) propionate, 2-ethylene-bis (4, 6-di-tert-butylphenol), tris (2, 4-di-tert-butylphenol) phosphite, dioctadecyl alcohol pentaerythritol diphosphite, bis (3, 5-di-tert-butylphenyl) pentaerythritol diphosphite and stearyl 3, 3-thiopropionate;
preferably, the black master batch is a mixture of toner and matrix resin;
preferably, the mass ratio of the toner to the matrix resin is (20-40): (60-80);
preferably, the toner is carbon black.
9. A method of making the thermally conductive junction box material of any of claims 1-8, comprising the steps of: and stirring and mixing the matrix resin, the heat-conducting filler, the compatilizer and the antioxidant according to the proportion, and performing extrusion granulation and drying to obtain the heat-conducting junction box material.
10. Use of a thermally conductive junction box material according to any of claims 1 to 8 for the preparation of a thermally conductive junction box.
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