CN104962048B8 - A kind of fiberglass reinforced fire retardant PBT material and preparation method thereof - Google Patents
A kind of fiberglass reinforced fire retardant PBT material and preparation method thereof Download PDFInfo
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 69
- 239000000463 material Substances 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title abstract description 5
- 239000011152 fibreglass Substances 0.000 title abstract description 4
- 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 abstract description 54
- 239000003365 glass fiber Substances 0.000 claims abstract description 22
- 239000004594 Masterbatch (MB) Substances 0.000 claims abstract description 20
- 239000004845 glycidylamine epoxy resin Substances 0.000 claims abstract description 12
- 239000006057 Non-nutritive feed additive Substances 0.000 claims abstract description 6
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical group O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 229920002302 Nylon 6,6 Polymers 0.000 claims description 8
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims description 8
- 229960001545 hydrotalcite Drugs 0.000 claims description 8
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 8
- 239000003822 epoxy resin Substances 0.000 claims description 6
- 229920000647 polyepoxide Polymers 0.000 claims description 6
- 239000004793 Polystyrene Substances 0.000 claims description 4
- 239000004417 polycarbonate Substances 0.000 claims description 4
- 229920000515 polycarbonate Polymers 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 229920002292 Nylon 6 Polymers 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims 2
- BSZXAFXFTLXUFV-UHFFFAOYSA-N 1-phenylethylbenzene Chemical compound C=1C=CC=CC=1C(C)C1=CC=CC=C1 BSZXAFXFTLXUFV-UHFFFAOYSA-N 0.000 claims 1
- AHIPJALLQVEEQF-UHFFFAOYSA-N 4-(oxiran-2-ylmethoxy)-n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1COC(C=C1)=CC=C1N(CC1OC1)CC1CO1 AHIPJALLQVEEQF-UHFFFAOYSA-N 0.000 claims 1
- -1 diglycidyl p-amino benzoic acid Chemical compound 0.000 claims 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 3
- 230000002708 enhancing effect Effects 0.000 abstract 2
- 229910052599 brucite Inorganic materials 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- 239000004033 plastic Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 13
- 230000015556 catabolic process Effects 0.000 description 7
- 238000001035 drying Methods 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- BZQKBFHEWDPQHD-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-[2-(2,3,4,5,6-pentabromophenyl)ethyl]benzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1CCC1=C(Br)C(Br)=C(Br)C(Br)=C1Br BZQKBFHEWDPQHD-UHFFFAOYSA-N 0.000 description 2
- CXXSQMDHHYTRKY-UHFFFAOYSA-N 4-amino-2,3,5-tris(oxiran-2-ylmethyl)phenol Chemical compound C1=C(O)C(CC2OC2)=C(CC2OC2)C(N)=C1CC1CO1 CXXSQMDHHYTRKY-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009775 high-speed stirring Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 238000005453 pelletization Methods 0.000 description 2
- 239000012748 slip agent Substances 0.000 description 2
- YOHIZYOYUGYYOO-UHFFFAOYSA-N 6-[bis(oxiran-2-ylmethyl)amino]-3-(oxiran-2-ylmethyl)cyclohexa-2,4-dien-1-one Chemical compound C(C1CO1)N(C1C(C=C(C=C1)CC1CO1)=O)CC1CO1 YOHIZYOYUGYYOO-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 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
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910052771 Terbium Inorganic materials 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 0.000 description 1
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
技术领域technical field
[0001]本发明涉及高分子材料领域,尤其涉及的是一种玻纤增强阻燃PBT材料。[0001] The present invention relates to the field of polymer materials, in particular to a glass fiber reinforced flame retardant PBT material.
背景技术Background technique
[0002]增强阻燃PBT材料大量应用于电子电器制品,电子电器制品要求材料不但具有优异的机械性能,同时要求具备好的电性能,特别是材料的漏电起痕指数和击穿电压这两个指标要求很高,而PBT阻燃体系所使用的阻燃剂多为卤系阻燃剂,但它们易从材料表面析出,腐蚀模具,并能产生大量导电离子及炭粒沉积物,促使电流泄露,大大降低材料的漏电起痕指数(以下简称CTI),同时材料的击穿电压也不高,通常低于225V。为获得高CTI值和高击穿电压的玻纤增强阻燃PBT材料,通常采用磷系或氮系来替代卤系阻燃剂,或者采取复配的手段,降低卤系阻燃剂的用量来达到提高CTI值的目的,但卤系阻燃剂的阻燃效率对PBT材料而言是最优的,所需的添加量也是相对较低,这为获得高的机械性能提供了可能性,因此,采用卤系阻燃剂阻燃PBT,同时要求获得较高的CTI值和较高击穿电压是急需解决的技术问题。Reinforced flame retardant PBT material is widely used in electronic and electrical products, and electronic and electrical products require materials not only to have excellent mechanical properties, but also to have good electrical properties, especially the tracking index and breakdown voltage of the material. The index requirements are very high, and the flame retardants used in the PBT flame retardant system are mostly halogen-based flame retardants, but they are easy to precipitate from the surface of the material, corrode the mold, and can generate a large number of conductive ions and carbon particle deposits, which promotes current leakage. , greatly reducing the tracking index (hereinafter referred to as CTI) of the material, and the breakdown voltage of the material is not high, usually lower than 225V. In order to obtain glass fiber reinforced flame-retardant PBT materials with high CTI value and high breakdown voltage, phosphorus-based or nitrogen-based flame retardants are usually used to replace halogen-based flame retardants, or compounding methods are used to reduce the amount of halogen-based flame retardants. To achieve the purpose of improving the CTI value, the flame retardant efficiency of halogen-based flame retardants is optimal for PBT materials, and the required addition amount is relatively low, which provides the possibility to obtain high mechanical properties, so , The use of halogen flame retardants to flame retardant PBT, while requiring a higher CTI value and a higher breakdown voltage is an urgent technical problem to be solved.
发明内容SUMMARY OF THE INVENTION
[0003]为解决上述技术问题,本发明提供一种玻纤增强阻燃PBT材料及其制备方法。[0003] In order to solve the above-mentioned technical problems, the present invention provides a kind of glass fiber reinforced flame-retardant PBT material and preparation method thereof.
[0004] —种玻纤增强阻燃PBT材料,包含以下组分(重量百分比):A kind of glass fiber reinforced flame-retardant PBT material, comprises following component (percent by weight):
[0005] PBT: 40% 〜70%PBT: 40%~70%
[0006] 阻燃母粒:18〜30%Flame retardant master batch: 18~30%
[0007] 玻璃纤维:1〜30%Glass fiber: 1~30%
[0008]缩水甘油胺类环氧树脂:0.1〜0.5%Glycidylamine epoxy resin: 0.1~0.5%
[0009]水滑石:0.1〜0.5%Hydrotalcite: 0.1~0.5%
[0010] 其他加工助剂:0.5〜1.0%Other processing aids: 0.5~1.0%
[0011] 所述PBT特性粘度0.7〜1.3;Described PBT intrinsic viscosity 0.7~1.3;
[0012]所述阻燃剂母粒包括主阻燃剂、阻燃协效剂和载体树脂。主阻燃剂是十溴二苯乙烷、溴化环氧树脂、溴化聚苯乙烯、溴化聚碳酸酯中的至少一种,阻燃协效剂是三氧化二锑,主阻燃剂和阻燃协效剂重量比为3:1或2:1或4:1,载体树脂为尼龙66树脂或尼龙6树脂,阻燃剂母粒中载体树脂重量百分比是30%,阻燃剂母粒中主阻燃剂和阻燃协效剂两者之和的重量比为70%;[0012] The flame retardant master batch includes a main flame retardant, a flame retardant synergist and a carrier resin. The main flame retardant is at least one of decabromodiphenylethane, brominated epoxy resin, brominated polystyrene and brominated polycarbonate, the flame retardant synergist is antimony trioxide, and the main flame retardant is The weight ratio of the flame retardant synergist is 3:1 or 2:1 or 4:1, the carrier resin is nylon 66 resin or nylon 6 resin, the weight percentage of the carrier resin in the flame retardant masterbatch is 30%, and the flame retardant masterbatch The weight ratio of the sum of the main flame retardant and the flame retardant synergist in the pellets is 70%;
[0013] 所述玻璃纤维为单丝直径10〜15μηι的无碱玻纤;Described glass fiber is the alkali-free glass fiber of monofilament diameter 10~15 μm;
[0014]所述缩水甘油胺类环氧树脂是三缩水甘油基对氨基苯酚、四缩水甘油-1,3-双氨甲基环己烷、Ν,Ν_ 二缩水甘油基-4-缩水甘油氧代苯胺、二异丙叉苯撑型四缩水甘油胺中的至少一种;缩水甘油胺类环氧树脂的作用是提高材料的CTI值;Described glycidylamine epoxy resin is triglycidyl-p-aminophenol, tetraglycidyl-1,3-bisaminomethyl cyclohexane, N,N-diglycidyl-4-glycidyl oxygen At least one of aniline and diisopropylidene tetraglycidylamine; the effect of glycidylamine epoxy resin is to improve the CTI value of the material;
[0015]所述水滑石的比表面积<15m2/g,水滑石的作用是提高CTI值,同时提高材料的击穿电压;The specific surface area of described hydrotalcite<15m / g, the effect of hydrotalcite is to improve CTI value, improve the breakdown voltage of material simultaneously;
[0016]所述其他加工助剂包括抗氧剂和润滑剂,如常用的抗氧剂1010,抗氧剂168,润滑剂EBS;[0016] The other processing aids include antioxidants and lubricants, such as commonly used antioxidant 1010, antioxidant 168, lubricant EBS;
[0017] 一种玻纤增强阻燃PBT材料的制备方法,包括两个步骤,第一步骤为阻燃母粒的制备,第二步骤为复合材料的共混挤出,具体如下所述:A kind of preparation method of glass fiber reinforced flame-retardant PBT material, comprises two steps, and the first step is the preparation of flame-retardant master batch, and the second step is the blending extrusion of composite material, specifically as follows:
[0018]第一步将PA66树脂、主阻燃剂、阻燃协效剂按照比例称量,在高速搅拌锅中搅拌3〜5分钟,然后加入到双螺杆挤出机挤出,挤出温度为250〜270度,真空度为0.04〜In the first step, PA66 resin, main flame retardant, flame retardant synergist are weighed according to the proportion, stirred 3~5 minutes in high-speed stirring pot, then join in twin-screw extruder and extrude, extruding temperature is 250~270 degrees, and the vacuum degree is 0.04~
0.08MPa,经水冷切粒包装制得阻燃母粒。将阻燃母粒放置在鼓风式干燥机中干燥后备用,干燥温度为120度,干燥时间4〜6小时。0.08MPa, the flame retardant masterbatch is obtained by water-cooled pelletizing and packaging. The flame retardant masterbatch is placed in a blast dryer for subsequent use after drying, the drying temperature is 120 degrees, and the drying time is 4 to 6 hours.
[0019]第二步将PBT树脂放置在鼓风式干燥机中干燥,干燥温度为120度,干燥时间4〜6小时。按比例称量PBT树脂、阻燃母粒倒入高速搅拌锅中搅拌I〜2分钟,倒入相应比例的缩水甘油胺类环氧树脂,搅拌I〜2分钟,最后倒入相应比例的水滑石和其他加工助剂,搅拌I〜2分钟,从双螺杆主喂料口加入挤出,玻纤从双螺杆的侧喂料口加入。挤出温度为230〜250度,真空度为0.04〜0.08MPa,经水冷切粒包装制得玻纤增强阻燃PBT材料。[0019] The second step is to place the PBT resin in a blast dryer to dry, and the drying temperature is 120 degrees, and the drying time is 4 to 6 hours. PBT resin, flame retardant master batch are weighed proportionally and poured into the high-speed stirring pot and stirred for 1 to 2 minutes, poured into corresponding proportion of glycidyl amine epoxy resin, stirred for 1 to 2 minutes, and finally poured into corresponding proportion of hydrotalcite With other processing aids, stir for 1 to 2 minutes, add extrusion from the twin-screw main feed port, and add glass fiber from the twin-screw side feed port. The extrusion temperature is 230~250 degrees, the vacuum degree is 0.04~0.08MPa, and the glass fiber reinforced flame retardant PBT material is obtained by water-cooled pelletizing and packaging.
具体实施方式detailed description
[0020] 对比例I〜5的配方如下表1:The formula of comparative example 1~5 is following table 1:
[0021] 表1:对比I〜5配方Table 1: contrast 1~5 formula
[0022][0022]
~~ 对比例I 对比例2 对比例3 对比例4 对比例5 一 ~~ Comparative Example I Comparative Example 2 Comparative Example 3 Comparative Example 4 Comparative Example 5 One
~PBT 特性粘度 L O ~58 _ 58 一 58 58 58 ~PBT Intrinsic Viscosity L O ~58 _ 58 - 58 58 58
主阻燃剂十溴二苯乙9 9Main flame retardant decabromodiphenyl ethyl 9 9
__^________^______
浪化环氧树 9 Wave Epoxy 9
__m________m______
溴化聚苯乙 9 Brominated polystyrene 9
__m________m______
漠化聚碳酸 9 Bromide polycarbonate 9
,.酷____________,.cool____________
阻燃协效剂_三氧Ih二锑 3___3_ 3 3__3 Flame Retardant Synergist_Trioxide Ih Antimony 3___3_ 3 3__3
3.璃纤维 — 30 一 30 30 ~30 ~30 ~ 3. Fiberglass — 30 a 30 30 ~30 ~30 ~
I丸铽剂 抗氧 1010 一 0.1 0.1 ~θ7ΐ 0.1 0.1 I pill terbium antioxidant 1010 a 0.1 0.1 ~θ7ΐ 0.1 0.1
— —抗氧剂 168 0.1 一 0.1 0.1 ~θΓΐ ~0.1 ~ — —Antioxidant 168 0.1 — 0.1 0.1 ~θΓΐ ~0.1 ~
Έ滑剂 I EBS I 0.1 I 0.1 0.1 I 0.1 I 0.1 ~ Έ slip agent I EBS I 0.1 I 0.1 0.1 I 0.1 I 0.1 ~
[0023] 实施例1〜5的配方如下表2:The formula of embodiment 1~5 is following table 2:
[0024] 表2:实施例1〜5配方Table 2: embodiment 1~5 formula
[0025][0025]
— 实施例1 实施例2 实施例3 实施例4 实施例5 ~ Tbt 特性粘度 1.0~ 53 — 53 53 ~53 53 — Example 1 Example 2 Example 3 Example 4 Example 5 ~ Tbt Intrinsic viscosity 1.0 ~ 53 — 53 53 ~ 53 53
Έ 燃母粒 一 17 17 17 ~Τ7 —17 ~ Έ Burning masterbatch one 17 17 17 ~Τ7 -17 ~
玻璃纤维 _ --一 30 30 ~30~30 ~30 —Fiberglass _ --one 30 30 ~30~30 ~30 —
一玩氧剂 _抗氧 1010 0.1 一 0.1 0.1 ~θΓΐ 0.1 ~ One play oxygen agent _ antioxidant 1010 0.1 one 0.1 0.1 ~θΓΐ 0.1 ~
—抗氧剂 168 一 0.1 0.1 ~α I 0.1 0.1 - Antioxidant 168 - 0.1 0.1 ~α I 0.1 0.1
Έ滑剂 ~EBS 0.1 一 0.1 0.1 0.1 "ο.1 ~ Έ slip agent ~EBS 0.1 - 0.1 0.1 0.1 "ο.1 ~
缩水甘油胺 οΠ 05 03 03Glycidamine οΠ 05 03 03
类环氧树腊_______Epoxy resin _______
IjR滑石 I 0.1 0.3 I 0.5 IjR Talc I 0.1 0.3 I 0.5
[0026]实施例1的阻燃母粒中的十溴二苯乙烷:三氧化二锑:尼龙66比为9:3: 5;实施例2的阻燃母粒中的溴化环氧树脂:三氧化二锑:尼龙66比为9:3:5,缩水甘油胺类环氧树脂是三缩水甘油基对氨基苯酚;Decabromodiphenylethane in the flame-retardant master batch of embodiment 1: antimony trioxide: nylon 66 ratio is 9:3: 5; The brominated epoxy resin in the flame-retardant master batch of embodiment 2 : The ratio of antimony trioxide: nylon 66 is 9:3:5, and the glycidylamine epoxy resin is triglycidyl-p-aminophenol;
[0027]实施例3的阻燃母粒中的溴化聚苯乙烯:三氧化二锑:尼龙66比为9:3:5,缩水甘油胺类环氧树脂是四缩水甘油-1,3-双氨甲基环己烷;The brominated polystyrene in the flame-retardant master batch of embodiment 3: antimony trioxide: nylon 66 ratio is 9:3:5, and glycidylamine epoxy resin is tetraglycidol-1,3- bisaminomethylcyclohexane;
[0028]实施例4的阻燃母粒中的溴化环氧树脂:三氧化二锑:尼龙66比为9:3:5,缩水甘油胺类环氧树脂是N,N-二缩水甘油基-4-缩水甘油氧代苯胺环氧树脂;实施例5的阻燃母粒中的溴化聚碳酸酯:三氧化二锑:尼龙66比为9:3:5,缩水甘油胺类环氧树脂是二异丙叉苯撑型四缩水甘油胺;The brominated epoxy resin in the flame-retardant master batch of embodiment 4: antimony trioxide: nylon 66 ratio is 9:3:5, and glycidylamine epoxy resin is N, N-diglycidyl -4-glycidyl oxoaniline epoxy resin; the brominated polycarbonate in the flame retardant master batch of Example 5: antimony trioxide: nylon 66 ratio is 9:3:5, glycidylamine epoxy resin is diisopropylidene tetraglycidylamine;
[0029] 对比例和实施例检测结果如下表3:Comparative example and embodiment detection result are following table 3:
[0030] 表3:对比例I〜5以及实施例1〜5检测数据Table 3: comparative example 1~5 and embodiment 1~5 detection data
[0031][0031]
测试项对比例对比例对比例对比例对比例实施例实施例实施例实施例实施例目/单 1 2 3 4 5 1 2 3 4 5 Test item Comparative Example Comparative Example Comparative Example Comparative Example
位___________Bit ___________
拉仲强118 121 118 ~123 120 121 119 120 123 120 La Zhongqiang 118 121 118 ~123 120 121 119 120 123 120
度/MPa___________Degree/MPa___________
Ifiiiis195 200 205 198 200 200 198 202 203 199Ifiiiis195 200 205 198 200 200 198 202 203 199
度/MPa___________Degree/MPa___________
缺口冲ΪΤΤ4 1273 10.5 11.1 12.0 12.7 13.0 11.5 10.8 12.3 击强度 Notched Impact ΪΤΤ4 1273 10.5 11.1 12.0 12.7 13.0 11.5 10.8 12.3 Impact Strength
/KJ/m2___________/KJ/m2___________
非缺 U4θΠ 38?9 37\5 404 39?5 42?8 39?8 ΪΠ 442~ 38.9 冲*强度 Not missing U4θΠ 38?9 37\5 404 39?5 42?8 39?8 ΪΠ 442~ 38.9 Punch*strength
/KJ/m2____________/KJ/m2____________
燃性 V-O V-O 一 V-O _ V-O V-O O V-O V-O 一 V-O V-OFlammability V-O V-O a V-O _ V-O V-O O V-O V-O a V-O V-O
CTI 值 Ϊ75 200 200 200 200 300 375 350 350 375 CTI value Ϊ75 200 200 200 200 300 375 350 350 375
JV___________JV___________
击穿电30 32 32 32 32 32 32 45 45 45 Breakdown 30 32 32 32 32 32 32 45 45 45
H?:3mm H?: 3mm
/KV __________/KV __________
[0032]从检测的结果可以发现:阻燃母粒、缩水甘油胺类环氧树脂、和水滑石可以提高CTI值,尤其是水滑石,不但可以提高CTI值,还提高了材料击穿电压。Can find from the result of detection: flame retardant master batch, glycidyl amine epoxy resin and hydrotalcite can improve CTI value, especially hydrotalcite, not only can improve CTI value, also improve material breakdown voltage.
[0033]其他实施例与相应的对比例得出的结论均和上述类似。PBT粘度0.7〜1.2,玻纤含量10〜30%之间,阻燃母粒中主阻燃剂为几种复配或载体树脂为尼龙6,均表现出表3得出的规律。[0033] The conclusions drawn by other embodiments and corresponding comparative examples are all similar to the above. The PBT viscosity is 0.7~1.2, the glass fiber content is between 10~30%, the main flame retardant in the flame retardant masterbatch is several compounds or the carrier resin is nylon 6, which all show the rules obtained in Table 3.
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