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对不同玻纤质量分数的LFT-PP粒料国标注塑样条,进行拉伸、弯曲、冲击等性能测试分析,结果表明:玻纤试样的拉伸强度、弯曲强度以及冲击强度均随玻纤质量分数的增加而提高;样品断裂延伸率随玻纤质量分数变化不明显,弯曲挠度随玻纤质量分数增加而减小;其中质量分数40%的玻纤试样拉伸强度达到145 MPa,弯曲强度高达170 MPa,简支梁缺口冲击强度为27 kJ/m2,表现出优异的力学性能.将质量分数40%玻纤的长纤粒料注塑成汽车翼子板制件,制品通过了汽车塑料制品各项测试并完成装配. 相似文献
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采用熔体浸渍工艺制备了长玻纤增强丙烯腈-丁二烯-苯乙烯共聚物(ABS)复合材料,研究了不同长玻纤含量对长玻纤增强ABS复合材料力学性能、动态力学性能和形态的影响。结果表明:随着长玻纤含量的增加,长玻纤增强ABS复合材料的力学性能和动态力学性能逐渐增加;长玻纤在基体树脂中具有良好的分散性。 相似文献
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采用长玻纤连续添加和短切玻纤制备了玻纤增强尼龙6(PA6)复合材料。主要考察了玻纤含量、玻纤种类以及挤出工艺条件对复合材料力学性能的影响,并利用扫描电子显微镜对复合材料的冲击断面和拉伸断面及玻纤形态进行了观察。结果表明,采用短切玻纤加入时,玻纤含量对GF/PA6复合材料的力学性能影响很大。随玻纤含量的增加,复合材料的力学性能越来越高,断裂伸长率变低。加工工艺参数对复合材料的力学性能有影响。采用长玻纤连续添加时,玻纤的添加位置对复合材料的性能影响不大。在玻纤含量相同时,采用长玻纤连续添加得到的材料力学性能明显优于采用短切玻纤时的性能。玻纤能均匀地分散在PA6基体中,玻纤的保留长度和长度分布对复合材料的性能有直接影响。 相似文献
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采用熔体浸渍工艺制备了高性能丙烯腈-丁二烯-苯乙烯共聚物(ABS)复合材料,利用动态热机械分析仪(DMA)对长玻纤增强ABS复合材料进行动态力学性能测试和表征,结果表明:玻纤含量和扫描频率对长玻纤增强ABS复合材料的动态力学性能有一定程度的影响,长玻纤增强复合材料的储能模量随着玻纤含量的增加而逐渐增加,复合材料的损耗因子随着扫描频率的增加而降低,同时采用Arrhenius方程计算长玻纤增强ABS复合材料在α转变时的分子运动活化能。另外,还研究了玻纤含量对长玻纤增强ABS复合材料力学性能的影响。 相似文献
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Long glass fiber (LGF)‐reinforced thermoplastic polyurethane (TPU) elastomers and polyoxymethylene (POM) (LGF/TPU/POM) composites were prepared by using self‐designed impregnation device. Dynamic mechanical properties of the LGF/TPU/POM composites have been investigated by using dynamic mechanical thermal analysis. The results indicated that the storage modulus and glass transition temperature of the composites increase with increasing the glass fibers content and scanning frequencies. In addition, the Arrhenius relationship has been used to calculate the activation energy of α‐transition of the LGF/TPU/POM composites. The thermal stability of the LGF/TPU/POM composites was investigated by thermogravimetric analysis. The consequence demonstrated that the thermal stability increase with augmenting the content of glass fibers. The mechanical properties of the composites are investigated by a universal testing machine and a ZBC‐4 Impact Pendulum. The results demonstrated the mechanical properties of the composites aggrandize with augmenting the glass fibers content. The good dispersion of the LGFs in the matrix resins is obtained from scanning electron micrographs. POLYM. COMPOS., 35:2067–2073, 2014. © 2014 Society of Plastics Engineers 相似文献
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Performance of long glass fiber‐reinforced polypropylene composites at different injection temperature 下载免费PDF全文
Long glass fiber‐reinforced polypropylene composites were prepared using self‐designed impregnation device. Effects of the different injection temperature on mechanical properties, crystallization, thermal, and dynamic mechanical properties of long glass fiber‐reinforced polypropylene composites were discussed. The differential scanning calorimetry (DSC) results indicate that the melting peak temperature of PP/LGF composites gradually reduced, however, the crystallinity of PP/LGF composites gradually increased with increasing injection temperature. Thermo‐gravimetric analyzer (TGA) results demonstrate that with increasing injection temperature, the temperature of the PP/LGF composites melt increased, the viscosity of the PP/LGF composites melt lowered, the mold filling of the PP/LGF composites melt was easy, the shear force of glass fiber was relatively low, which made the residual length of glass fiber in products increase. Dynamic thermal mechanical analyzer (DMA) results show that the storage modulus of PP/LGF composites is the highest while the injection temperature is at 290°C, and the peak value of tan σ of PP /LGF composites at 290°C is minimal, which indicates that the mechanical properties of PP /LGF composites at 290°C is the best. What' more, the injection temperature at 290°C significantly ameliorated “glass fiber rich skin” of products of glass fiber‐reinforced composites. J. VINYL ADDIT. TECHNOL., 24:233–238, 2018. © 2016 Society of Plastics Engineers 相似文献
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Long glass fiber–reinforced thermoplastic composites were prepared by a new process, in situ solid‐state polycondensation (INSITU SSP). In this process reinforcing continuous fibers were impregnated by the oligomer of PET melt, and then the impregnated continuous fibers were cut to a desired length (designated prepreg); finally, the prepreg was in situ polymerized in the solid state to form the high molecular weight matrix. SEM, FTIR spectra, short‐beam shear stress test, flexural strength test, impact strength test, and the intrinsic viscosity measurement were used to investigate the wetting and interfacial adhesion, the mechanical properties of the composite, and the molecular weight of matrix resin in the composite. The results showed that the molecular weight of PET in the matrix resin and mechanical properties could be adjusted by controlling the SSP time and that the high level of interfacial adhesion between reinforcing fibers and matrix resin could be achieved by this novel INSITU SSP process, which are attributed to the good wetting of reinforcing fibers with low molecular weight oligomer melt as the impregnation fluid, the in situ formation of chemical grafting of oligomer chains onto the reinforcing fiber surface, and the in situ formation of the high molecular weight PET chains in the interphase regions. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91:3959–3965, 2004 相似文献
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Effect of impregnation time on performance of long glass fiber‐reinforced polypropylene composites 下载免费PDF全文
Long glass fiber (LGF)‐reinforced polypropylene (PP) composites were prepared using self‐designed impregnation device. Effects of impregnation time on mechanical properties, crystallization, dynamic mechanical properties, and morphology of PP/LGF composites were investigated. The experiment results demonstrate that the excellent tensile strength, Notched Izod impact strength was 152.9 MPa, 31.2 KJ/m2, respectively, and the stiffness of PP/LGF composites was higher, when the impregnation time was 7.03 s. The excellent interfacial adhesion between PP and glass fiber indicates that PP/LGF composites possess the outstanding mechanical properties. The impregnation time scarcely influenced thermal properties of PP/LGF composites. J. VINYL ADDIT. TECHNOL., 24:174–178, 2018. © 2016 Society of Plastics Engineers 相似文献
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采用熔体浸渍技术制备了长玻璃纤维母料(LGF/PP-g-MAH/PP)增强聚丙烯(PP)复合材料(LGF/PP)。通过双螺杆挤出机制备了同等配比的短玻纤增强聚丙烯(SGF/PP)复合材料。研究了LGF含量、环氧树脂(EP)和固化剂(2E4MZ)对LGF/PP复合材料的力学性能影响。结果表明:当LGF质量分数为35%~40%时,LGF/PP的综合力学性能最好,且明显优于同样组成的SGF/PP复合材料。EP和含固化剂(2E4MZ)的EP对LGF/PP复合材料的力学性能提高有一定的作用。SEM照片分析表明:EP的加入能改善玻纤与聚丙烯基体的界面粘接。 相似文献
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Structural composites with a high content of renewable material were produced from natural fibres and an acrylated epoxidized soybean oil resin. Composites were prepared by spray impregnation followed by compression moulding at elevated temperature. The resulting composites had good mechanical properties in terms of tensile strength and flexural strength. Tensile testing as well as dynamical mechanical thermal analysis showed that increasing the fibre content, increased the mechanical properties. The resin can be reinforced with up to 70 wt % fibre without sacrifice in processability. The tensile modulus ranged between 5.8 and 9.7 GPa depending on the type of fibre mat. The study of the adhesion by low vacuum scanning electron microscopy shows that the fibres are well impregnated in the matrix. The aging properties were finally evaluated. This study shows that composites with a very high content of renewable constituents can be produced from soy bean oil resins and natural fibres. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
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Summary: Long glass fiber reinforced PA6 (LGF/PA6) prepregs were prepared by impregnating PA6 oligomer melt into reinforcing glass fiber followed by subsequent solid‐state polymerization (SSP) to obtain LGF/PA6 composite pellets. A conventional injection‐molding machine suitable for short glass fiber reinforced composites was applied to the processing of the prepared composites, which reduced the fiber length in the final products. Mechanical properties, thermal property, and fiber length distribution of injection molding bars were investigated. Scanning electron microscopy (SEM) was used to observe the impact fracture surfaces and the surfaces of glass fiber after the SSP. It was found that the LGF/PA6 composites were of favorable mechanical properties, especially the impact strength, although the average length of glass fiber was rather short. By this novel process, the content of glass fiber in composite could be high up to 60 wt.‐% and the maximum level of heat distortion temperature (HDT) was close to the melting temperature of PA6. SEM images indicated the favorable interfacial properties between the glass fiber and matrix. The glass fiber surfaces were further observed by SEM after removing the matrix PA6 with a solvent, the results showed that PA6 macromolecules were grafted onto the surface. Furthermore, the grafting amount of PA6 was increased with SSP time.