CN104151768A - Carbon fiber reinforced ABS (Acrylonitrile Butadiene Styrene) resin composite material with superior heat conductivity and preparation method - Google Patents
Carbon fiber reinforced ABS (Acrylonitrile Butadiene Styrene) resin composite material with superior heat conductivity and preparation method Download PDFInfo
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- CN104151768A CN104151768A CN201410394791.0A CN201410394791A CN104151768A CN 104151768 A CN104151768 A CN 104151768A CN 201410394791 A CN201410394791 A CN 201410394791A CN 104151768 A CN104151768 A CN 104151768A
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- carbon fiber
- abs resin
- composite material
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- thermal conductivity
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- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 title claims abstract description 107
- 229920000049 Carbon (fiber) Polymers 0.000 title claims abstract description 91
- 239000004917 carbon fiber Substances 0.000 title claims abstract description 91
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 title claims abstract description 74
- 239000000463 material Substances 0.000 title claims abstract description 43
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- 239000000805 composite resin Substances 0.000 title claims abstract description 17
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 title description 22
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 title description 22
- 239000002131 composite material Substances 0.000 claims abstract description 47
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000007822 coupling agent Substances 0.000 claims abstract description 18
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 15
- 239000000314 lubricant Substances 0.000 claims abstract description 15
- 239000011256 inorganic filler Substances 0.000 claims abstract description 14
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 14
- 238000012545 processing Methods 0.000 claims abstract description 14
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 13
- 239000002994 raw material Substances 0.000 claims abstract description 11
- 238000011049 filling Methods 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 15
- 239000000395 magnesium oxide Substances 0.000 claims description 9
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 9
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical group O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 7
- 238000001125 extrusion Methods 0.000 claims description 7
- -1 polydimethylsiloxane Polymers 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- OKOBUGCCXMIKDM-UHFFFAOYSA-N Irganox 1098 Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NCCCCCCNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 OKOBUGCCXMIKDM-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 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 claims description 2
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 claims description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 2
- 239000005909 Kieselgur Substances 0.000 claims description 2
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 2
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical group CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 claims description 2
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 claims description 2
- 239000003063 flame retardant Substances 0.000 claims description 2
- 239000011521 glass Substances 0.000 claims description 2
- 238000001746 injection moulding Methods 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 239000004571 lime Substances 0.000 claims description 2
- 239000010445 mica Substances 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- 239000004005 microsphere Substances 0.000 claims description 2
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims description 2
- 239000008188 pellet Substances 0.000 claims description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 claims 1
- WYZYEMMUIFWWAE-UHFFFAOYSA-N [SiH4].CCCOC(=O)C(C)=C Chemical compound [SiH4].CCCOC(=O)C(C)=C WYZYEMMUIFWWAE-UHFFFAOYSA-N 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 239000012761 high-performance material Substances 0.000 claims 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 13
- 230000017525 heat dissipation Effects 0.000 abstract description 11
- 238000010924 continuous production Methods 0.000 abstract description 8
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- VNWKTOKETHGBQD-YPZZEJLDSA-N carbane Chemical group [10CH4] VNWKTOKETHGBQD-YPZZEJLDSA-N 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 20
- 239000011295 pitch Substances 0.000 description 14
- 239000011159 matrix material Substances 0.000 description 11
- 238000000465 moulding Methods 0.000 description 10
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 6
- 230000006872 improvement Effects 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 229910021393 carbon nanotube Inorganic materials 0.000 description 2
- 239000002041 carbon nanotube Substances 0.000 description 2
- 239000003575 carbonaceous material Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000011231 conductive filler Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 229910021389 graphene Inorganic materials 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 229910021392 nanocarbon Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MTEZSDOQASFMDI-UHFFFAOYSA-N 1-trimethoxysilylpropan-1-ol Chemical compound CCC(O)[Si](OC)(OC)OC MTEZSDOQASFMDI-UHFFFAOYSA-N 0.000 description 1
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004918 carbon fiber reinforced polymer Substances 0.000 description 1
- 239000011294 coal tar pitch Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002715 modification method Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- UIDUKLCLJMXFEO-UHFFFAOYSA-N propylsilane Chemical compound CCC[SiH3] UIDUKLCLJMXFEO-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000011257 shell material Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
本发明涉及导热性能优良的碳纤维增强ABS树脂复合材料及制备方法,该复合材料由以下重量份的材料组成:ABS树脂90份,马来酸酐接枝ABS10份,碳纤维10~80份,无机填料10~20份,偶联剂0.5~5份,抗氧剂0.2~1份以及润滑剂0~3份;按照配比称取各组分原料;将除碳纤维以外的各组分原料高速混合;所得混合物料加入双螺杆挤出机料斗,将碳纤维于挤出机加纤口加入,挤出造粒。与现有技术相比,本发明提供的复合材料刚性高、散热性能好,适用于薄壁化、轻量化电子/电气产品的生产加工;并且原材料成本低、制备工艺简单,适合于工业化连续生产。The invention relates to a carbon fiber reinforced ABS resin composite material with excellent thermal conductivity and a preparation method thereof. The composite material is composed of the following materials in parts by weight: 90 parts of ABS resin, 10 parts of maleic anhydride grafted ABS, 10-80 parts of carbon fiber, and 10 parts of inorganic filler ~20 parts, 0.5~5 parts of coupling agent, 0.2~1 part of antioxidant and 0~3 parts of lubricant; weigh the raw materials of each component according to the proportion; mix the raw materials of each component except carbon fiber at high speed; the obtained The mixed material is added to the hopper of the twin-screw extruder, and the carbon fiber is added to the fiber-filling port of the extruder to extrude and granulate. Compared with the prior art, the composite material provided by the present invention has high rigidity and good heat dissipation performance, and is suitable for the production and processing of thin-walled and lightweight electronic/electrical products; and the cost of raw materials is low, and the preparation process is simple, which is suitable for industrialized continuous production .
Description
技术领域technical field
本发明属于碳纤维复合材料技术领域,具体涉及一种导热性能优良的碳纤维增强热塑性ABS树脂复合材料及其制备方法。The invention belongs to the technical field of carbon fiber composite materials, and in particular relates to a carbon fiber reinforced thermoplastic ABS resin composite material with excellent thermal conductivity and a preparation method thereof.
背景技术Background technique
ABS树脂是指丙烯腈-丁二烯-苯乙烯共聚物,它无毒、无味、吸水率低,力学性能、热性能、耐磨性、抗化学药品性和染色性良好,成型加工和机械加工性较好,广泛用于冰箱内衬、电视机外壳、吸尘器、空调器、电话、仪表、计算机、复印机等电子电器工业中。随着社会发展和工业进步,电子元器件和电子设备越来越向着薄壁、轻量、小型化方面发展,因此对材料的刚性及导热性的要求越来越高。例如笔记本电脑要做的薄、轻、小,这就要求笔记本外壳材料、CPU材料以及各种集成电路板材料的模量高、刚性大,抵抗外力变形的能力强,才能减小厚度;还要导热性好,才能改善电脑散热问题,从而提高电脑的运行速度和稳定性。为了提高ABS树脂的刚性和导热性,ABS resin refers to acrylonitrile-butadiene-styrene copolymer, which is non-toxic, tasteless, low water absorption, mechanical properties, thermal properties, wear resistance, chemical resistance and dyeability, good molding and mechanical processing Good performance, widely used in refrigerator lining, TV casing, vacuum cleaner, air conditioner, telephone, instrument, computer, copier and other electronic and electrical industries. With social development and industrial progress, electronic components and electronic equipment are becoming more and more thin-walled, lightweight, and miniaturized. Therefore, the requirements for the rigidity and thermal conductivity of materials are getting higher and higher. For example, notebook computers need to be thin, light, and small, which requires notebook shell materials, CPU materials, and various integrated circuit board materials to have high modulus, high rigidity, and strong resistance to external force deformation, so as to reduce the thickness; Good thermal conductivity can improve the cooling problem of the computer, thereby improving the running speed and stability of the computer. In order to improve the rigidity and thermal conductivity of ABS resin,
高分子材料刚性和散热性的提高均可采用复合改性方法。为提高ABS树脂的刚性,往往可以通过玻璃纤维、碳纤维等增强复合的方法,其中增强用的碳纤维主要采用聚丙烯腈基碳纤维,所以这些方法不能够提高ABS的导热性。为提高ABS的散热性(实质是热导率),通常采用填充高热导率的填料粒子,制备填充型导热复合材料。常用的导热填料包括一、金属填料,如银、铜、铝、镁、镍等粉末;二、无机非金属填料,如氮化铝、氮化硼、氧化镁、碳化硅等氮化物、氧化物、碳化物等;三、具有石墨结构的碳材料,如石墨烯、碳纳米管、纳米碳纤维及沥青基碳纤维(文献1:短纤维/A B S树脂复合材料导电导热性能研究,化工新型材料,2014,Vol.42,No.4,p103~106)等。但是金属导热填料存在密度大、有腐蚀性以及带来ABS材料力学性能下降等缺点;无机非金属填料对ABS树脂导热性提高并不是很有效果,往往也会使ABS树脂力学性能下降。而采用碳材料如石墨烯、碳纳米管及纳米碳纤维等的方法虽然能够显著提高ABS树脂的导热性,但这些材料价格昂贵,尚不能工业化生产,所涉及的技术更是仅仅停留在实验室研究阶段。文献1采用ABS树脂的丙酮溶液浸渍到自制的沥青基碳纤维中、经过真空抽取溶剂再进行热压成型的方法制备了导热ABS/沥青碳纤维复合材料,该方法制备工艺复杂,且残留在材料内部的有机溶剂会导致力学性能下降等危害,工业上完全不可行;此外,还存在不适合制备复杂结构的产品、材料只具有一维及二维导热性以及力学性能没有得到提高等问题。Composite modification methods can be used to improve the rigidity and heat dissipation of polymer materials. In order to improve the rigidity of ABS resin, it is often possible to strengthen composite methods such as glass fiber and carbon fiber. Among them, the carbon fiber used for reinforcement is mainly polyacrylonitrile-based carbon fiber, so these methods cannot improve the thermal conductivity of ABS. In order to improve the heat dissipation of ABS (essentially thermal conductivity), filler particles with high thermal conductivity are usually used to prepare filled thermal conductive composite materials. Commonly used thermally conductive fillers include 1. Metal fillers, such as silver, copper, aluminum, magnesium, nickel and other powders; 2. Inorganic non-metallic fillers, such as aluminum nitride, boron nitride, magnesium oxide, silicon carbide and other nitrides and oxides , carbides, etc.; 3. Carbon materials with graphite structure, such as graphene, carbon nanotubes, nanocarbon fibers and pitch-based carbon fibers (Document 1: Research on electrical and thermal conductivity of short fiber/ABS resin composite materials, new chemical materials, 2014, Vol.42, No.4, p103-106), etc. However, metal thermally conductive fillers have the disadvantages of high density, corrosion, and the decline in the mechanical properties of ABS materials; inorganic non-metallic fillers are not very effective in improving the thermal conductivity of ABS resins, and often reduce the mechanical properties of ABS resins. Although the method of using carbon materials such as graphene, carbon nanotubes and nano-carbon fibers can significantly improve the thermal conductivity of ABS resin, these materials are expensive and cannot be industrialized, and the technologies involved are only in laboratory research. stage. Document 1 prepared the thermally conductive ABS/pitch carbon fiber composite material by impregnating the acetone solution of ABS resin into the self-made pitch-based carbon fiber, vacuuming the solvent, and then hot-pressing. Organic solvents can lead to hazards such as degradation of mechanical properties, and are completely unfeasible in industry. In addition, there are still problems such as not suitable for the preparation of products with complex structures, materials with only one-dimensional and two-dimensional thermal conductivity, and mechanical properties that have not been improved.
发明内容Contents of the invention
本发明的目的就是为了克服上述现有技术存在的缺陷而提供一种可同时显著提高材料的力学性能和导热性能、原材料成本低、制备工艺简单的适用于工业化连续生产的导热性能优良的碳纤维增强ABS树脂复合材料及制备方法。The purpose of the present invention is to overcome the defects of the above-mentioned prior art and provide a carbon fiber-reinforced carbon fiber-reinforced carbon fiber with excellent thermal conductivity suitable for industrial continuous production, which can significantly improve the mechanical properties and thermal conductivity of the material at the same time, with low raw material cost and simple preparation process. ABS resin composite material and preparation method thereof.
本发明的目的可以通过以下技术方案来实现:一种导热性能优良的碳纤维增强ABS树脂复合材料,其特征在于,该复合材料由以下重量份的材料组成:ABS树脂90份,马来酸酐接枝ABS10份,碳纤维10~80份,无机填料10~20份,偶联剂0.5~5份,抗氧剂0.2~1份以及润滑剂0~3份。The object of the present invention can be achieved through the following technical solutions: a carbon fiber reinforced ABS resin composite material with excellent thermal conductivity, characterized in that the composite material is made up of the following materials by weight: 90 parts of ABS resin, grafted with maleic anhydride 10 parts of ABS, 10-80 parts of carbon fiber, 10-20 parts of inorganic filler, 0.5-5 parts of coupling agent, 0.2-1 part of antioxidant and 0-3 parts of lubricant.
所述的ABS树脂选自挤出级、注塑级、填充级或阻燃级的粒料或粉料中的一种。The ABS resin is selected from pellets or powders of extrusion grade, injection molding grade, filling grade or flame retardant grade.
所述的碳纤维的含量为10~80份,当短碳纤维含量小于10份时,无法在ABS树脂基体内形成完善的导热通道,所以对ABS树脂导热性能的提高不显著。碳纤维含量越高,ABS树脂的力学性能和导热性能越高。但是当短碳纤维的质量百分比过高,其含量大于80份时,对混合设备的磨损严重,缩短螺杆的使用寿命。另外,含量过高会使复合材料的熔融粘度高、熔体流动性下降,因而对成型加工带来不利,尤其不利于薄壁、复杂结构制品的成型。The content of the carbon fiber is 10-80 parts. When the short carbon fiber content is less than 10 parts, a perfect heat conduction channel cannot be formed in the ABS resin matrix, so the improvement of the thermal conductivity of the ABS resin is not significant. The higher the carbon fiber content, the higher the mechanical properties and thermal conductivity of ABS resin. However, when the mass percentage of short carbon fibers is too high and its content is greater than 80 parts, the wear and tear on the mixing equipment will be serious, and the service life of the screw will be shortened. In addition, if the content is too high, the melt viscosity of the composite material will be high and the melt fluidity will be reduced, which will be unfavorable to the molding process, especially unfavorable to the molding of thin-walled and complex structural products.
所述的碳纤维是热导率大于200W/(mK),拉伸模量大于700GPa的高性能沥青基碳纤维。可以选用商品化的系列的K1392U,K13C6U,K13D2U,K63A12或者Cytec系列的P-1002K,P-100S 2K,P-1202K,P-120S 2K等沥青基碳纤维,也可以是其他的具有相当模量及热导率的沥青基碳纤维。The carbon fiber is a high-performance pitch-based carbon fiber with a thermal conductivity greater than 200W/(mK) and a tensile modulus greater than 700GPa. commercialized series K1392U, K13C6U, K13D2U, K63A12 or Cytec P-1002K, P-100S 2K, P-1202K, P-120S 2K and other pitch-based carbon fibers, or other pitch-based carbon fibers with comparable modulus and thermal conductivity.
所述的碳纤维是短切碳纤维,平均长度为10μm~2mm。当纤维长度小于10μm时,不利于纤维在ABS树脂基体内形成连续的热传导通路,不能够有效提高ABS树脂的热传导性能;所以,纤维长度值越大越有利于提高材料的强度、模量以及热传导性。但是当纤维长度大于2mm时,将造成复合材料熔融粘度高,流动性差,给后续的制品的成型加工带来困难,尤其不利于薄壁、复杂结构制品的成型加工。The carbon fibers are chopped carbon fibers with an average length of 10 μm to 2 mm. When the fiber length is less than 10 μm, it is not conducive to the fiber to form a continuous heat conduction path in the ABS resin matrix, and the heat conduction performance of the ABS resin cannot be effectively improved; therefore, the larger the fiber length value, the better the strength, modulus and thermal conductivity of the material. . However, when the fiber length is greater than 2 mm, the composite material will have high melt viscosity and poor fluidity, which will bring difficulties to the subsequent molding and processing of products, especially not conducive to the molding and processing of thin-walled and complex structural products.
所述的无机填料选自滑石粉、玻璃微珠、碳酸钙、硫酸钡、氧化镁、硫酸钙、硅石灰、云母粉、硅藻土或蒙脱土中的一种或一种以上。优选重量比1∶3∶1的滑石粉、氧化镁和氧化铝混合物。The inorganic filler is selected from one or more of talcum powder, glass microspheres, calcium carbonate, barium sulfate, magnesium oxide, calcium sulfate, silica lime, mica powder, diatomaceous earth or montmorillonite. A mixture of talc, magnesium oxide and aluminum oxide in a weight ratio of 1:3:1 is preferred.
所述的偶联剂选自乙烯基三乙氧基硅烷、γ-氨丙基三乙氧基硅烷、γ-氨丙基三甲氧基硅烷、γ-甲基丙烯酸丙酯基硅烷、γ-缩水甘油醚氧丙基三甲氧基硅烷、正钛酸四异丙酯、异丙基三异十八酰钛酸酯或聚酯改性聚二甲基硅氧烷中的一种或一种以上。优选重量比1∶1的γ-氨丙基三乙氧基硅烷和γ-缩水甘油醚氧丙基三甲氧基硅烷。The coupling agent is selected from vinyltriethoxysilane, γ-aminopropyltriethoxysilane, γ-aminopropyltrimethoxysilane, γ-methacrylate propyl silane, γ-shrink One or more of glyceryl ether oxypropyl trimethoxysilane, tetraisopropyl orthotitanate, isopropyl triisostearyl titanate or polyester-modified polydimethylsiloxane. Preference is given to gamma-aminopropyltriethoxysilane and gamma-glycidoxypropyltrimethoxysilane in a weight ratio of 1:1.
所述的抗氧剂选自四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯,N,N’-双-(3-(3,5-二叔丁基-4-羟基苯基)丙酰基)己二胺或三[2,4-二叔丁基苯基]亚磷酸酯中的一种或一种以上;The antioxidant is selected from tetrakis[β-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid]pentaerythritol ester, N,N'-bis-(3-(3,5-di One or more of tert-butyl-4-hydroxyphenyl)propionyl)hexamethylenediamine or tris[2,4-di-tert-butylphenyl]phosphite;
所述的润滑剂选自乙撑双脂肪酸酰胺、乙烯-丙烯酸共聚物或硅酮粉中的一种或一种以上。The lubricant is selected from one or more of ethylene bis fatty acid amide, ethylene-acrylic acid copolymer or silicone powder.
一种导热性能优良的碳纤维增强ABS树脂复合材料的制备方法,其特征在于,包括以下步骤:A method for preparing a carbon fiber reinforced ABS resin composite material with excellent thermal conductivity, characterized in that it comprises the following steps:
(1)将原料碳纤维、ABS树脂和马来酸酐接枝ABS充分干燥;(1) fully drying raw material carbon fiber, ABS resin and maleic anhydride grafted ABS;
(2)按照配比称取各组分原料;(2) taking each component raw material according to the proportioning ratio;
(3)将除碳纤维以外的各组分原料高速混合;(3) High-speed mixing of raw materials of each component except carbon fiber;
(4)将步骤(3)所得混合物料加入双螺杆挤出机料斗,将碳纤维于挤出机加纤口加入,挤出造粒。(4) Put the mixed material obtained in step (3) into the hopper of the twin-screw extruder, add carbon fiber at the fiberizing port of the extruder, and extrude to pelletize.
步骤(1)中所述干燥的条件是在70~90℃下鼓风干燥4~6小时,加工前的含水量必须小于0.02wt%。碳纤维具有吸湿性,加工前的干燥很重要,否则将导致ABS树脂高温加工过程中的降解,导致力学性能下降。The drying condition in the step (1) is blast drying at 70-90° C. for 4-6 hours, and the water content before processing must be less than 0.02 wt%. Carbon fiber is hygroscopic, and drying before processing is very important, otherwise it will lead to the degradation of ABS resin during high temperature processing, resulting in a decrease in mechanical properties.
所述的步骤(4)中所述双螺杆挤出机自喂料口至挤出机模头的六区温度设定分别为150℃、175℃、185℃、195℃、195℃、200℃,主机转速20~50赫兹。The temperature settings of the six zones of the twin-screw extruder from the feeding port to the die head of the extruder in the step (4) are respectively 150°C, 175°C, 185°C, 195°C, 195°C, and 200°C , The host speed is 20-50 Hz.
本发明采用ABS树脂90份,马米酸酐接枝ABS10份作为树脂基体,由于马来酸酐极性分子的可再反应性和强极性,添加马来酸酐接枝ABS可以有效提高基体与碳纤维的结合性能,促进碳纤维的分散,有利于在材料内部形成碳纤维导热通路。The present invention adopts 90 parts of ABS resin and 10 parts of maleic anhydride grafted ABS as the resin matrix. Due to the reactivity and strong polarity of maleic anhydride polar molecules, adding maleic anhydride grafted ABS can effectively improve the bond between the matrix and carbon fibers. Combined with properties, it promotes the dispersion of carbon fibers and is conducive to the formation of carbon fiber heat conduction paths inside the material.
沥青基碳纤维是以石油重油沥青、煤焦油沥青或萘系等稠环芳烃化合物为原料制备的碳纤维,按照性能可分为通用级沥青基碳纤维和高性能沥青碳纤维两类。高性能沥青碳纤维具有密度小、模量高(最高已达930GPa,达到理论值的91%)、导热性优异(热导率高达600~800W/(mK),是金属中导热性最好的铜的1.5~2倍)、和热膨胀系数小等优点。利用沥青基碳纤维增强ABS树脂所制备的复合材料,既能够大幅度提高ABS树脂的模量(刚性),满足电子/电气制品薄壁化、轻量化的要求,同时又能够大幅度提高ABS树脂的导热性能。此外,由于沥青基碳纤维热膨胀系数极低,还能够提高ABS树脂制品的尺寸稳定性,有利于制造高精度尺寸的产品。复合材料的力学性能受到纤维含量、界面等因素影响;而导热性能的提高需要在聚合物基体中形成更多的连续热传导通路,受到纤维本身的导热性能、含量、分散等因素影响,本发明人综合考虑这些影响因素,通过对复合工艺的调整、螺杆组合及转速及各种助剂的选配等方面进行大量研究,完成了本发明。Pitch-based carbon fiber is a carbon fiber prepared from petroleum heavy oil pitch, coal tar pitch, or naphthalene-based condensed ring aromatic compounds. According to its performance, it can be divided into two types: general-purpose pitch-based carbon fiber and high-performance pitch carbon fiber. High-performance pitch carbon fiber has low density, high modulus (up to 930GPa, reaching 91% of the theoretical value), excellent thermal conductivity (thermal conductivity as high as 600-800W/(mK), and is the copper with the best thermal conductivity among metals. 1.5 to 2 times of that), and a small coefficient of thermal expansion. The composite material prepared by using pitch-based carbon fiber to reinforce ABS resin can not only greatly improve the modulus (rigidity) of ABS resin, meet the requirements of thin-walled and lightweight electronic/electrical products, but also can greatly improve ABS resin. thermal conductivity. In addition, due to the extremely low thermal expansion coefficient of pitch-based carbon fiber, it can also improve the dimensional stability of ABS resin products, which is conducive to the manufacture of products with high precision dimensions. The mechanical properties of composite materials are affected by factors such as fiber content and interface; and the improvement of thermal conductivity needs to form more continuous heat conduction paths in the polymer matrix, which is affected by factors such as thermal conductivity, content, and dispersion of the fibers themselves. The inventors Considering these influencing factors comprehensively, the present invention has been completed through a lot of research on the adjustment of the composite process, screw combination and rotation speed, and selection of various auxiliary agents.
与现有技术相比,本发明有效克服了填充ABS树脂力学性能、导热性能二者不能兼顾的以往技术的缺点,制备了一种力学性能和导热性能够同时得到提高的碳纤维增强ABS热塑性复合材料,适合用来制造薄壁化、轻量化的电子/电气产品,可极大扩展ABS树脂材料的应用领域。且复合材料的原料成本低、制备工艺简单、适合于工业连续化生产。Compared with the prior art, the present invention effectively overcomes the shortcomings of the prior art that the mechanical properties and thermal conductivity of the filled ABS resin cannot be balanced, and prepares a carbon fiber reinforced ABS thermoplastic composite material that can simultaneously improve the mechanical properties and thermal conductivity , suitable for the manufacture of thin-walled and lightweight electronic/electrical products, which can greatly expand the application fields of ABS resin materials. Moreover, the raw material cost of the composite material is low, the preparation process is simple, and it is suitable for industrial continuous production.
具体实施方式Detailed ways
下面结合具体实施例对本发明进行详细说明。The present invention will be described in detail below in conjunction with specific embodiments.
实施例及比较例中使用的ABS树脂的密度为1.07g/cm3,熔融指数MFR=3g/10min,弯曲模量为2.3GPa,弯曲强度为58MPa,热导率为0.17W/(mK)。马来酸酐接枝ABS为市售产品,碳纤维为高性能沥青基碳纤维,密度为2.16g/cm3,拉伸模量为650GPa,拉伸强度为2.1GPa,热导率为350W/(mK)。加工前在碳纤维和树脂均在90℃下连续鼓风干燥4小时,使含水量均小于0.02wt%。The ABS resin used in Examples and Comparative Examples has a density of 1.07g/cm 3 , a melt index MFR=3g/10min, a flexural modulus of 2.3GPa, a flexural strength of 58MPa, and a thermal conductivity of 0.17W/(mK). Maleic anhydride grafted ABS is a commercially available product, the carbon fiber is a high-performance pitch-based carbon fiber, the density is 2.16g/cm 3 , the tensile modulus is 650GPa, the tensile strength is 2.1GPa, and the thermal conductivity is 350W/(mK) . Before processing, both the carbon fiber and the resin are continuously air-dried at 90° C. for 4 hours, so that the water content is less than 0.02 wt%.
力学性能用万能电子拉力机测量,热导率用激光闪射法导热系数测量仪测量。纤维长度用热分解后统计500~600根长度再取平均值的方法。The mechanical properties were measured with a universal electronic tensile machine, and the thermal conductivity was measured with a laser flash thermal conductivity measuring instrument. The fiber length is calculated by counting the lengths of 500-600 fibers after thermal decomposition and taking the average value.
实施例1Example 1
称取重量份含量ABS树脂90份,马来酸酐接枝ABS10份,碳纤维10份,无机填料(滑石粉、氧化镁和氧化铝,重量比1∶3∶1)10份,偶联剂(γ-氨丙基三乙氧基硅烷和γ-缩水甘油醚氧丙基三甲氧基硅烷,重量比1∶1)0.5份,抗氧剂(四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯)0.2份以及润滑剂0份配料;将ABS树脂、马来酸酐接枝ABS树脂、无机填料、偶联剂、抗氧剂及润滑剂等投入高速混合机中高速混合均匀,下料至挤出机料斗,碳纤维于挤出机加纤口加入,控制自喂料口至挤出机模头的各区温度分别为150℃、175℃、185℃、195℃、195℃、200℃,主机转速50赫兹,经过双螺杆挤出机挤出造粒即可得到该复合材料。Take by weight 90 parts of content ABS resin, 10 parts of maleic anhydride grafted ABS, 10 parts of carbon fiber, 10 parts of inorganic filler (talcum powder, magnesium oxide and aluminum oxide, weight ratio 1: 3: 1), coupling agent (γ -Aminopropyltriethoxysilane and γ-glycidyloxypropyltrimethoxysilane, weight ratio 1:1) 0.5 parts, antioxidant (tetrakis[β-(3,5-di-tert-butyl- 4-hydroxyphenyl) propionic acid] pentaerythritol ester) 0.2 part and lubricant 0 part batching; ABS resin, maleic anhydride grafted ABS resin, inorganic filler, coupling agent, antioxidant and lubricant etc. are put into high-speed mixing Mix evenly in the machine at high speed, feed to the hopper of the extruder, add carbon fiber at the fiber feeding port of the extruder, control the temperature of each zone from the feeding port to the die head of the extruder to be 150°C, 175°C, 185°C, 195°C °C, 195 °C, 200 °C, the speed of the main machine is 50 Hz, and the composite material can be obtained by extruding and granulating through a twin-screw extruder.
本实施例的试样内碳纤维的平均长度为485μm,复合材料的各性能分别为:弯曲模量9.3GPa,弯曲强度95MPa,热导率2.2W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂材料的4.0倍、1.6倍和12.9倍,刚性和散热性能得到显著,满足薄壁化、轻量化的电子/电气产品成型加工的要求,可极大扩展ABS树脂的应用领域。且复合材料的制备工艺简单、挤出过程持续稳定,适合于工业连续化生产。The average length of the carbon fiber in the sample of this embodiment is 485 μm, and the properties of the composite material are respectively: flexural modulus 9.3 GPa, flexural strength 95 MPa, thermal conductivity 2.2 W/(mK). The flexural modulus, strength and thermal conductivity are respectively 4.0 times, 1.6 times and 12.9 times that of pure ABS resin materials, and the rigidity and heat dissipation performance are significantly improved, which meets the requirements of thin-walled and lightweight electronic/electrical product molding and processing. Greatly expand the application field of ABS resin. Moreover, the preparation process of the composite material is simple, the extrusion process is continuous and stable, and is suitable for industrial continuous production.
实施例2Example 2
称取重量份含量ABS树脂90份,马来酸酐接枝ABS10份,碳纤维80份,无机填料(滑石粉、氧化镁和氧化铝,重量比1∶3∶1)10份,偶联剂(γ-氨丙基三乙氧基硅烷和γ-缩水甘油醚氧丙基三甲氧基硅烷,重量比1∶1)5份,抗氧剂(四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯)1份以及润滑剂(乙撑双脂肪酸酰胺)3份配料;将ABS树脂、马来酸酐接枝ABS树脂、无机填料、偶联剂、抗氧剂及润滑剂等投入高速混合机中高速混合均匀,下料至挤出机料斗,碳纤维于挤出机加纤口加入,控制自喂料口至挤出机模头的各区温度分别为150℃、175℃、185℃、195℃、195℃、200℃,主机转速50赫兹,经过双螺杆挤出机挤出造粒即可得到该复合材料。Take by weight 90 parts of content ABS resin, 10 parts of maleic anhydride grafted ABS, 80 parts of carbon fiber, 10 parts of inorganic filler (talcum powder, magnesium oxide and aluminum oxide, weight ratio 1: 3: 1), coupling agent (γ -Aminopropyltriethoxysilane and γ-glycidyloxypropyltrimethoxysilane, weight ratio 1:1) 5 parts, antioxidant (tetrakis[β-(3,5-di-tert-butyl- 4-hydroxyphenyl) propionic acid] pentaerythritol ester) 1 part and lubricant (ethylene bisfatty acid amide) 3 parts of ingredients; ABS resin, maleic anhydride grafted ABS resin, inorganic filler, coupling agent, antioxidant and lubricants are put into the high-speed mixer and mixed evenly at high speed, and the material is fed to the hopper of the extruder, and the carbon fiber is added at the fiber feeding port of the extruder. 175°C, 185°C, 195°C, 195°C, 200°C, the speed of the main engine is 50 Hz, and the composite material can be obtained by extruding and granulating through a twin-screw extruder.
本实施例的试样内碳纤维的平均长度为102μm,复合材料的各性能分别为:弯曲模量31.5GPa,弯曲强度260MPa,热导率3.4W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的13.7倍、4.5倍和20.0倍,刚性和散热性能得到显著,满足薄壁化、轻量化的电子/电气产品成型加工的要求,可极大扩展ABS树脂的应用领域。且复合材料的制备工艺简单、挤出过程持续稳定,适合于工业连续化生产。The average length of the carbon fiber in the sample of this embodiment is 102 μm, and the properties of the composite material are respectively: flexural modulus 31.5 GPa, flexural strength 260 MPa, thermal conductivity 3.4 W/(mK). The flexural modulus, strength and thermal conductivity are respectively 13.7 times, 4.5 times and 20.0 times that of pure ABS resin, and the rigidity and heat dissipation performance are significantly improved, meeting the requirements of thin-walled and lightweight electronic/electrical product molding and processing, and can be extremely Greatly expand the application field of ABS resin. Moreover, the preparation process of the composite material is simple, the extrusion process is continuous and stable, and is suitable for industrial continuous production.
实施例3Example 3
称取重量份含量ABS树脂90份,马来酸酐接枝ABS10份,碳纤维40份,无机填料(滑石粉、氧化镁和氧化铝,重量比1∶3∶1)10份,偶联剂(γ-氨丙基三乙氧基硅烷和γ-缩水甘油醚氧丙基三甲氧基硅烷,重量比1∶1)2份,抗氧剂(四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯)0.6份以及润滑剂(乙撑双脂肪酸酰胺)1份配料;将ABS树脂、马来酸酐接枝ABS树脂、无机填料、偶联剂、抗氧剂及润滑剂等投入高速混合机中高速混合均匀,下料至挤出机料斗,碳纤维于挤出机加纤口加入,控制自喂料口至挤出机模头的各区温度分别为150℃、175℃、185℃、195℃、195℃、200℃,主机转速50赫兹,经过双螺杆挤出机挤出造粒即可得到该复合材料。Take by weight 90 parts of content ABS resin, 10 parts of maleic anhydride grafted ABS, 40 parts of carbon fiber, 10 parts of inorganic filler (talcum powder, magnesium oxide and aluminum oxide, weight ratio 1: 3: 1), coupling agent (γ -Aminopropyltriethoxysilane and γ-glycidyloxypropyltrimethoxysilane, weight ratio 1:1) 2 parts, antioxidant (tetrakis[β-(3,5-di-tert-butyl- 4-hydroxyphenyl) propionic acid] pentaerythritol ester) 0.6 part and lubricant (ethylene bis fatty acid amide) 1 part batching; ABS resin, maleic anhydride grafted ABS resin, inorganic filler, coupling agent, antioxidant and lubricants are put into the high-speed mixer and mixed evenly at high speed, and the material is fed to the hopper of the extruder, and the carbon fiber is added at the fiber feeding port of the extruder. 175°C, 185°C, 195°C, 195°C, 200°C, the speed of the main engine is 50 Hz, and the composite material can be obtained by extruding and granulating through a twin-screw extruder.
本实施例的试样内碳纤维的平均长度为396μm,复合材料的各性能分别为:弯曲模量16.3GPa,弯曲强度150MPa,热导率2.6W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的7.1倍、2.6倍和15.3倍,刚性和散热性能得到显著,满足薄壁化、轻量化的电子/电气产品成型加工的要求,可极大扩展ABS树脂的应用领域。且复合材料的制备工艺简单、挤出过程持续稳定,适合于工业连续化生产。The average length of the carbon fiber in the sample of this embodiment is 396 μm, and the properties of the composite material are respectively: flexural modulus 16.3 GPa, flexural strength 150 MPa, and thermal conductivity 2.6 W/(mK). The flexural modulus, strength and thermal conductivity are 7.1 times, 2.6 times and 15.3 times that of pure ABS resin, respectively, and the rigidity and heat dissipation performance are significantly improved, meeting the requirements of thin-walled and lightweight electronic/electrical product molding and processing, and can be extremely Greatly expand the application field of ABS resin. Moreover, the preparation process of the composite material is simple, the extrusion process is continuous and stable, and is suitable for industrial continuous production.
实施例4Example 4
称取重量份含量ABS树脂90份,马来酸酐接枝ABS10份,碳纤维40份,无机填料(滑石粉、氧化镁和氧化铝,重量比1∶3∶1)20份,偶联剂(γ-氨丙基三乙氧基硅烷和γ-缩水甘油醚氧丙基三甲氧基硅烷,重量比1∶1)2份,抗氧剂(N,N’-双-(3-(3,5-二叔丁基-4-羟基苯基)丙酰基)己二胺)0.6份以及润滑剂(硅酮粉)1份配料;将ABS树脂、马来酸酐接枝ABS树脂、无机填料、偶联剂、抗氧剂及润滑剂等投入高速混合机中高速混合均匀,下料至挤出机料斗,碳纤维于挤出机加纤口加入,控制自喂料口至挤出机模头的各区温度分别为150℃、175℃、185℃、195℃、195℃、200℃,主机转速50赫兹,经过双螺杆挤出机挤出造粒即可得到该复合材料。Take by weight 90 parts of content ABS resin, 10 parts of maleic anhydride grafted ABS, 40 parts of carbon fiber, 20 parts of inorganic filler (talcum powder, magnesium oxide and aluminum oxide, weight ratio 1: 3: 1), coupling agent (γ -Aminopropyltriethoxysilane and γ-glycidyloxypropyltrimethoxysilane, weight ratio 1:1) 2 parts, antioxidant (N, N'-bis-(3-(3,5 -di-tert-butyl-4-hydroxyphenyl)propionyl)hexamethylenediamine) 0.6 part and lubricant (silicone powder) 1 part of ingredients; ABS resin, maleic anhydride grafted ABS resin, inorganic filler, coupling The additives, antioxidants and lubricants are put into the high-speed mixer and mixed evenly at high speed, and the material is fed to the hopper of the extruder. The carbon fiber is added at the fiber feeding port of the extruder, and the temperature of each zone from the feeding port to the die head of the extruder is controlled. 150°C, 175°C, 185°C, 195°C, 195°C, 200°C respectively, the main engine speed is 50 Hz, and the composite material can be obtained by extruding and granulating through a twin-screw extruder.
本实施例的试样内碳纤维的平均长度为324μm,复合材料的各性能分别为:弯曲模量17.1GPa,弯曲强度163MPa,热导率2.9W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的7.4倍、2.8倍和17.1倍,刚性和散热性能得到显著,满足薄壁化、轻量化的电子/电气产品成型加工的要求,可极大扩展ABS树脂的应用领域。且复合材料的制备工艺简单、挤出过程持续稳定,适合于工业连续化生产。The average length of the carbon fiber in the sample of this embodiment is 324 μm, and the properties of the composite material are respectively: flexural modulus of 17.1 GPa, flexural strength of 163 MPa, and thermal conductivity of 2.9 W/(mK). The flexural modulus, strength and thermal conductivity are 7.4 times, 2.8 times and 17.1 times that of pure ABS resin, respectively, and the rigidity and heat dissipation performance are significantly improved, meeting the requirements of thin-walled and lightweight electronic/electrical product molding and processing, and can be extremely Greatly expand the application field of ABS resin. Moreover, the preparation process of the composite material is simple, the extrusion process is continuous and stable, and is suitable for industrial continuous production.
实施例5Example 5
称取重量份含量ABS树脂90份,马来酸酐接枝ABS10份,碳纤维40份,无机填料(滑石粉、氧化镁和氧化铝,重量比1∶3∶1)15份,偶联剂(γ-氨丙基三乙氧基硅烷和γ-缩水甘油醚氧丙基三甲氧基硅烷,重量比1∶1)2份,抗氧剂(N,N’-双-(3-(3,5-二叔丁基-4-羟基苯基)丙酰基)己二胺)0.6份以及润滑剂(硅酮粉)1份配料;将ABS树脂、马来酸酐接枝ABS树脂、无机填料、偶联剂、抗氧剂及润滑剂等投入高速混合机中高速混合均匀,下料至挤出机料斗,碳纤维于挤出机加纤口加入,控制自喂料口至挤出机模头的各区温度分别为150℃、175℃、185℃、195℃、195℃、200℃,主机转速50赫兹,经过双螺杆挤出机挤出造粒即可得到该复合材料。Take by weight 90 parts of content ABS resin, 10 parts of maleic anhydride grafted ABS, 40 parts of carbon fiber, 15 parts of inorganic filler (talcum powder, magnesium oxide and aluminum oxide, weight ratio 1: 3: 1), coupling agent (γ -Aminopropyltriethoxysilane and γ-glycidyloxypropyltrimethoxysilane, weight ratio 1:1) 2 parts, antioxidant (N, N'-bis-(3-(3,5 -di-tert-butyl-4-hydroxyphenyl)propionyl)hexamethylenediamine) 0.6 part and lubricant (silicone powder) 1 part of ingredients; ABS resin, maleic anhydride grafted ABS resin, inorganic filler, coupling The additives, antioxidants and lubricants are put into the high-speed mixer and mixed evenly at high speed, and the material is fed to the hopper of the extruder. The carbon fiber is added at the fiber feeding port of the extruder, and the temperature of each zone from the feeding port to the die head of the extruder is controlled. 150°C, 175°C, 185°C, 195°C, 195°C, 200°C respectively, the main engine speed is 50 Hz, and the composite material can be obtained by extruding and granulating through a twin-screw extruder.
本实施例的试样内碳纤维的平均长度为338μm,复合材料的各性能分别为:弯曲模量16.8GPa,弯曲强度159MPa,热导率2.7W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的7.3倍、2.7倍和15.9倍,刚性和散热性能得到显著,满足薄壁化、轻量化的电子/电气产品成型加工的要求,可极大扩展ABS树脂的应用领域。且复合材料的制备工艺简单、挤出过程持续稳定,适合于工业连续化生产。The average length of the carbon fiber in the sample of this embodiment is 338 μm, and the properties of the composite material are respectively: flexural modulus of 16.8 GPa, flexural strength of 159 MPa, and thermal conductivity of 2.7 W/(mK). The flexural modulus, strength and thermal conductivity are 7.3 times, 2.7 times and 15.9 times that of pure ABS resin, respectively, and the rigidity and heat dissipation performance are significantly improved, meeting the requirements of thin-walled and lightweight electronic/electrical product molding and processing, and can be extremely Greatly expand the application field of ABS resin. Moreover, the preparation process of the composite material is simple, the extrusion process is continuous and stable, and is suitable for industrial continuous production.
比较例1Comparative example 1
复合材料组成中碳纤维含量为5份,其它组成和制备方法和实施例1相同。The carbon fiber content in the composition of the composite material is 5 parts, and other compositions and preparation methods are the same as in Example 1.
所制备复合材料试样内碳纤维的平均长度为602μm,复合材料的各性能分别为:弯曲模量7.3GPa,弯曲强度78MPa,热导率0.52W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的3.2倍、1.3和3.1倍。和实施例1比较,本比例中碳纤维的添加量过低,无法对ABS树脂起到增强作用,也无法在ABS树脂基体内形成热传导通路,因此材料的刚性和散热性能都没有明显改善。The average length of the carbon fibers in the prepared composite material sample is 602 μm, and the properties of the composite material are: flexural modulus 7.3 GPa, flexural strength 78 MPa, and thermal conductivity 0.52 W/(mK). The flexural modulus, strength and thermal conductivity are 3.2 times, 1.3 and 3.1 times that of pure ABS resin, respectively. Compared with Example 1, the amount of carbon fiber added in this ratio is too low to strengthen the ABS resin, and cannot form a heat conduction path in the ABS resin matrix, so the rigidity and heat dissipation performance of the material are not significantly improved.
比较例2Comparative example 2
复合材料组成中碳纤维含量为100份,其它组成和制备方法和实施例1相同。The carbon fiber content in the composition of the composite material is 100 parts, and other compositions and preparation methods are the same as in Example 1.
所制备复合材料试样内碳纤维的平均长度为73μm,复合材料的各性能分别为:弯曲模量34.2GPa,弯曲强度252MPa,热导率2.4W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的14.9倍、4.3倍和14.1倍。和实施例2比较,本比例中虽然提高了碳纤维的添加量,但是模量略有提高,而强度、热导率反而下降。这可能是基体粘度过高而使碳纤维分散性差造成的。由于碳纤维比ABS树脂价格高,碳纤维用量增加还将导致复合材料的成本增加。The average length of the carbon fibers in the prepared composite sample is 73 μm, and the properties of the composite are: flexural modulus 34.2 GPa, flexural strength 252 MPa, and thermal conductivity 2.4 W/(mK). The flexural modulus, strength and thermal conductivity are 14.9 times, 4.3 times and 14.1 times of pure ABS resin respectively. Compared with Example 2, although the addition amount of carbon fiber is increased in this ratio, the modulus is slightly increased, but the strength and thermal conductivity are decreased instead. This may be caused by the high viscosity of the matrix and the poor dispersion of carbon fibers. Since carbon fiber is more expensive than ABS resin, an increase in the amount of carbon fiber will also lead to an increase in the cost of composite materials.
比较例3Comparative example 3
复合材料组成中偶联剂含量为0,其它组成和制备方法和实施例5相同。The coupling agent content in the composition of the composite material is 0, and other compositions and preparation methods are the same as in Example 5.
所制备复合材料试样内碳纤维的平均长度为421μm,复合材料的各性能分别为:弯曲模量11.1GPa,弯曲强度108MPa,热导率0.36W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的4.8倍、1.9倍和2.1倍。和实施例5相比较,本例中没有添加偶联剂,因此纤维和树脂基体之间界面结合性差,还将导致纤维分散性差,难以在材料内部形成导热通路,所以ABS树脂的强度、模量及散热性能均得不到明显提高。The average length of the carbon fibers in the prepared composite sample is 421 μm, and the properties of the composite are: flexural modulus 11.1 GPa, flexural strength 108 MPa, and thermal conductivity 0.36 W/(mK). The flexural modulus, strength and thermal conductivity are 4.8 times, 1.9 times and 2.1 times of pure ABS resin respectively. Compared with Example 5, no coupling agent is added in this example, so the interfacial bonding between the fiber and the resin matrix is poor, which will also lead to poor fiber dispersion, and it is difficult to form a heat conduction path inside the material, so the strength and modulus of ABS resin and thermal performance were not significantly improved.
比较例4Comparative example 4
复合材料组成中ABS树脂含量取100份,马来酸酐接枝ABS的含量为0,其它组成和制备方法和实施例5相同。The content of ABS resin in the composition of the composite material is 100 parts, the content of maleic anhydride grafted ABS is 0, and other compositions and preparation methods are the same as in Example 5.
所制备复合材料试样内碳纤维的平均长度为447μm,复合材料的各性能分别为:弯曲模量6.3GPa,弯曲强度80MPa,热导率0.25W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的2.7倍、1.4倍和1.5倍。和实施例5相比较,本例中虽然添加了偶联剂,但是基体树脂中没有添加马来酸酐接枝ABS,因此纤维和树脂基体之间界面结合性差,还将导致纤维分散性差,难以在材料内部形成导热通路,所以ABS树脂的强度、模量及散热性能均得不到明显提高。The average length of the carbon fiber in the prepared composite material sample is 447 μm, and the properties of the composite material are: flexural modulus 6.3 GPa, flexural strength 80 MPa, thermal conductivity 0.25 W/(mK). The flexural modulus, strength and thermal conductivity are 2.7 times, 1.4 times and 1.5 times of pure ABS resin respectively. Compared with Example 5, although a coupling agent is added in this example, maleic anhydride grafted ABS is not added in the matrix resin, so the interfacial bonding between the fiber and the resin matrix is poor, and it will also lead to poor fiber dispersion, which is difficult in The heat conduction path is formed inside the material, so the strength, modulus and heat dissipation performance of ABS resin are not significantly improved.
比较例5Comparative Example 5
复合材料组成中ABS树脂含量取100份,马来酸酐接枝ABS的含量为0,偶联剂的含量为0,其它组成和制备方法和实施例5相同。In the composition of the composite material, the content of ABS resin is 100 parts, the content of maleic anhydride grafted ABS is 0, the content of coupling agent is 0, and other compositions and preparation methods are the same as in Example 5.
所制备复合材料试样内碳纤维的平均长度为416μm,复合材料的各性能分别为:弯曲模量5.6GPa,弯曲强度71MPa,热导率0.23W/(mK)。弯曲模量、强度及热导率分别为纯ABS树脂的2.4倍、1.2倍和1.4倍。和实施例5相比较,本例中既没有添加偶联剂,也没有添加马来酸酐接枝ABS,导致纤维和树脂基体之间界面结合性极差,并严重影响碳纤维的分散,难以在材料内部形成导热通路,所以ABS树脂的强度、模量及散热性能均得不到明显提高。The average length of the carbon fibers in the prepared composite material sample is 416 μm, and the properties of the composite material are: flexural modulus 5.6 GPa, flexural strength 71 MPa, and thermal conductivity 0.23 W/(mK). The flexural modulus, strength and thermal conductivity are 2.4 times, 1.2 times and 1.4 times of pure ABS resin respectively. Compared with Example 5, neither coupling agent nor maleic anhydride grafted ABS was added in this example, which resulted in extremely poor interfacial bonding between the fiber and the resin matrix, and seriously affected the dispersion of the carbon fiber, making it difficult to add carbon fiber to the material. A heat conduction path is formed inside, so the strength, modulus and heat dissipation performance of ABS resin are not significantly improved.
以上实施例的说明只是用于帮助理解本发明的方法及其核心思想。应该指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以对本发明进行若干改进和修饰,这些改进和修饰也落入本发明权利要求的保护范围内。The descriptions of the above embodiments are only used to help understand the method and core idea of the present invention. It should be pointed out that for those skilled in the art, without departing from the principles of the present invention, some improvements and modifications can be made to the present invention, and these improvements and modifications also fall within the protection scope of the claims of the present invention.
对所公开的实施例的上述说明,使本领域专业技术人员能够实现或使用本发明。对这些实施例的多种修饰对本领域的专业技术人员来说将是显而易见的,本文中所定义的一般原理可以在不脱离本发明的精神或范围的情况下,在其它实施例中实现。因此,本发明将不会被限制于本文所示的这些实施例,而是要符合与本文所公开的原理和新颖特点相一致的最宽的范围。The above description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the invention. Various modifications to these examples will be readily apparent to those skilled in the art, and the general principles defined herein may be implemented in other examples without departing from the spirit or scope of the invention. Therefore, the present invention will not be limited to the embodiments shown herein, but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
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Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102093692A (en) * | 2011-02-25 | 2011-06-15 | 四川飞亚新材料有限公司 | Polycarbonate (PC)/ acrylonitrile butadiene styrene (ABS) conductive alloy material and preparation method and use thereof |
KR20110070300A (en) * | 2009-12-18 | 2011-06-24 | 주식회사 삼양사 | Thermoplastic resin composition |
CN102558749A (en) * | 2012-01-04 | 2012-07-11 | 黑龙江大学 | Acrylonitrile butadiene-stvrene (ABS) resin/ conductive carbon black/ pitch-based carbon fiber conductive composite material and preparation method thereof |
CN103073836A (en) * | 2013-02-05 | 2013-05-01 | 武汉科技大学 | High thermal conductivity carbon fiber resin-based composite material and preparation method thereof |
CN103421270A (en) * | 2012-05-25 | 2013-12-04 | 上海杰事杰新材料(集团)股份有限公司 | ABS material and preparation method thereof |
CN103483761A (en) * | 2013-09-17 | 2014-01-01 | 安徽科聚新材料有限公司 | Fiber-reinforced ABS material and preparation method thereof |
-
2014
- 2014-08-12 CN CN201410394791.0A patent/CN104151768A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20110070300A (en) * | 2009-12-18 | 2011-06-24 | 주식회사 삼양사 | Thermoplastic resin composition |
CN102093692A (en) * | 2011-02-25 | 2011-06-15 | 四川飞亚新材料有限公司 | Polycarbonate (PC)/ acrylonitrile butadiene styrene (ABS) conductive alloy material and preparation method and use thereof |
CN102558749A (en) * | 2012-01-04 | 2012-07-11 | 黑龙江大学 | Acrylonitrile butadiene-stvrene (ABS) resin/ conductive carbon black/ pitch-based carbon fiber conductive composite material and preparation method thereof |
CN103421270A (en) * | 2012-05-25 | 2013-12-04 | 上海杰事杰新材料(集团)股份有限公司 | ABS material and preparation method thereof |
CN103073836A (en) * | 2013-02-05 | 2013-05-01 | 武汉科技大学 | High thermal conductivity carbon fiber resin-based composite material and preparation method thereof |
CN103483761A (en) * | 2013-09-17 | 2014-01-01 | 安徽科聚新材料有限公司 | Fiber-reinforced ABS material and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
张玉龙: "《塑料配方及其组分设计宝典》", 31 October 2005 * |
益小苏等: "《中国材料工程大典》", 31 March 2006 * |
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US11920076B2 (en) | 2017-10-13 | 2024-03-05 | Tokyo University Of Science Foundation | Fire retardant material |
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