聚丙烯/亚麻纤维复合材料的成型工艺及力学性能研究

选取聚丙烯(PP)纤维为基体材料,亚麻纤维为增强材料。运用正交设计法,探讨了PP/亚麻纤维复合材料的模压成型工艺。研究分析了两种纤维的质量比、模压温度、热压保温时间对复合材料力学性能的影响。结果表明,两种纤维的质量比为50:50、模压温度为180℃、热压保温时间为60min时,PP/亚麻纤维复合材料的力学性能最佳。     

黄麻纤维增强聚丙烯的力学性能

本文讨论了注塑成型黄麻纤维增强聚丙烯的制备方法和力学性能.将纤维重量含量分别为10%、20%和30%的复合材料进行比较,分析纤维含量对复合材料拉伸、弯曲和冲击性能的影响;将纤维分别切成约3mm、5mm和10mm长制成复合材料进行比较,分析纤维长度对复合材料拉伸、弯曲和冲击性能的影响.掺入黄麻纤维能使聚丙烯的拉伸和弯曲性能提高,但使其冲击强度降低;随纤维含量的增加或纤维长度的增加,复合材料的强度和模量是递增的,而冲击强度是递减的.     

竹原纤维增强复合材料的研究

竹原纤维与低熔点聚酯纤维及聚丙烯纤维的混合纤维集合体加工成非织造物,再经热压成型后,制成竹原纤维增强聚酯、聚丙烯热塑性树脂复合材料板材,并与竹原/亚麻纤维增强聚酯、聚丙烯热塑性树脂复合材料进行性能对比,进一步探讨这种复合材料板材的最佳制作工艺。鉴于这种材料可以被用于汽车和建筑等领域,通过对材料力学性能测试结果的模糊综合评判,选出性能最优的复合材料为竹原纤维/LMPET(40/60),在模压温度、时间、压力分别为165℃,30min和30MPa的条件下,所压制复合材料的纵向拉伸强度为136MPa,横向为87·58MPa;纵向弯曲强度为534MPa,横向为470MPa。     

汽车内饰用酚醛树脂/黄麻纤维复合材料的拉伸性能

采用正交试验方法,用5%Na OH溶液对黄麻毡进行预处理,利用模压成型工艺制备酚醛树脂/黄麻纤维复合材料,通过对正交试验结果进行极差分析和方差分析,研究树脂含量、模具温度、模具压力和保压时间4个工艺参数对复合材料拉伸性能的影响程度和显著性水平,并通过多指标综合评分法对材料的拉伸性能综合评价,分析各个工艺参数对材料拉伸性能的影响规律。结果显示,树脂含量和模具压力对复合材料的拉伸性能影响非常显著,当树脂含量为20%、模具温度为180℃、模具压力为10 MPa、模压时间为6 min时,复合材料的拉伸性能最好,此时拉伸强度为24.06 MPa,拉伸弹性模量为113.17 MPa。     

亚麻纤维增强聚丙烯基复合材料的隔声性能研究

以亚麻纤维为原料,聚丙烯为基体,制备纤维含量分别为0%、10%、20%、30%、40%的纤维增强复合材料,并对亚麻纤维进行碱处理和偶联剂处理,探讨了纤维含量以及表面处理对亚麻纤维增强复合材料的隔声性的影响。研究结果表明,当纤维含量超过10%时,复合材料的隔声性随着发声频率增加出现先增大后减小的趋势,同一发声频率,含量越低,隔声性能越差,当纤维含量超过30%后,电压峰值衰减率反而下降;表面处理后,复合材料的隔声性能有所提高,偶联剂处理后复合材料的隔声性能优于碱处理后的复合材料。     

PLA/剑麻纤维复合材料的增韧改性

利用聚乙二醇(PEG)、聚丁二酸丁二醇酯(PBS)对聚乳酸(PLA)/剑麻纤维(SF)复合材料进行增韧改性,PLA/SF复合体系与增韧剂PEG、PBS密炼共混后,经模压制备PL/A/SF纤维复合材料.通过正交实验,考察PEG含量、PBS含量、硬脂酸含量以及密炼温度对复合材料力学性能的影响.结果表明:PEG的含量对复合材料韧性的影响最显著.PBS的含量和硬脂酸的含量对复合材料冲击性能的影响比较显著,但对其断裂伸长率和拉伸强度的影响不显著.温度对复合材料的冲击性能和拉伸强度几乎没影响,但对其断裂伸长率的影响比较显著.     

亚麻纤维增强热固性树脂复合材料板材的研究

本文以亚麻纤维作为原料,经过针刺工艺制得亚麻纤维针刺毡,作为复合材料的增强体.通过改变纤维、热固性树脂种类,利用真空辅助RTM方法及模压法制备复合材料板材.对板材进行了拉伸及弯曲性能测试,比较了不同纤维和树脂的结合情况,进一步阐述了板材破坏机理.     

竹纤维-聚丙烯复合材料板材的成型工艺研究及优化

以竹纤维作为增强材料,聚丙烯纤维作为基体材料,通过正交设计不同模压成型工艺,在平板硫化机上压制出了竹纤维-聚丙烯复合材料板材。通过对竹纤维-聚丙烯复合材料的力学性能测试及对比分析,得出结论:模压温度对复合材料性能的影响较大,而模压保温时间的影响较小;在180℃、40 min时制得的竹纤维-聚丙烯复合材料具有良好的断裂强度;在170℃、40 min时制得的复合材料具有良好的顶破强度。     

锦葵纤维增强聚丙烯基复合材料力学性能研究

分别制备了锦葵纤维含量为10 %（质量分数,下同）、20 %、30 %、40 %和50 %的锦葵纤维增强增强聚丙烯基复合材料,研究了纤维含量对该复合材料拉伸性能和弯曲性能的影响,并与苎麻纤维增强聚丙烯基复合材料进行了对比。结果表明,随着锦葵纤维含量的增加,锦葵纤维增强聚丙烯基复合材料的拉伸强度和拉伸弹性模量逐渐增加,而弯曲强度和弯曲弹性模量呈现先增大后减小的趋势,当纤维含量为40 %时达最大值;纤维含量均为30 %时,除拉伸弹性模量外,锦葵纤维增强聚丙烯基复合材料的各项指标均低于苎麻纤维增强聚丙烯基复合材料。     

聚丙烯自增强复合材料层压板的制备和性能研究

以聚丙烯树脂为基体,聚丙烯纤维织物为增强体,采用层压成型工艺制备了聚丙烯自增强复合材料层压板。研究了成型温度、成型压力、成型时间和纤维含量等工艺参数对聚丙烯自增强复合材料层压板拉伸和弯曲性能的影响规律,并采用差示扫描量热(DSC)仪和扫描电子显微镜(SEM)对其进行了热分析和形态结构的表征。结果表明,当成型温度为175℃,成型压力为10 MPa,成型时间为15 min,纤维含量为60%时,聚丙烯自增强复合材料层压板的力学性能达到最大值,其拉伸强度为(125.76±0.77)MPa,弯曲强度和弯曲弹性模量分别为(30.77±0.70)MPa和(1 795.46±75.95)MPa;从DSC图和SEM图观察到成型温度为175℃时聚丙烯纤维表面发生了熔融,有利于纤维和树脂之间的界面粘结力的增强。     

Naturally compatible: Starch acetate/cellulosic fiber composites. I. Processing and properties

Composite compounds based on hemp and flax fibers in triethyl citrate plasticized starch acetate were prepared by melt processing. For better properties and processability, compounds with plasticizer contents in the range 20–35 wt% were screened. Composites were prepared with fiber contents up to 50 wt%. The composite mechanical properties were measured from injection molded test specimens. A Young's modulus of 8.3 GPa and stress at maximum load of 51 MPa were obtained with 40 wt% flax fiber in a plasticized starch acetate with 20 wt% triethyl citrate. Decreasing the plasticizer and increasing the fiber content, the tensile properties were consistently improved. An almost linear relation between fiber content and the tensile properties was found. The increase of the fiber content first improved the impact strength, but at higher fiber contents resulted in a reduction of impact strength. The quality of the produced materials was found to be good; the variation in properties between duplicated compounds was acceptable low, the variation in density and fiber content along a single tensile specimen was low, and finally, the porosity content was low even at high fiber content. The latter result was verified with scanning electron microscope images of fracture surfaces of the composites. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

Experimental investigation of the influence of the compounding process and the composite composition on the mechanical properties of a short flax fiber–reinforced polypropylene composite

Polypropylene (PP) composites containing 20 wt% short flax fibers are prepared, and the process parameters such as throughput, rotational speed, and screw configuration are varied during melt compounding with a corotating intermeshing twin‐screw extruder. The investigations reveal that low rotational speeds, high throughputs, and moderate shear energy inputs by the screw configuration led to an optimum set of mechanical properties. To investigate the influence of different composite compositions on the mechanical properties, composites with fiber contents between 0 and 40 wt% and maleic anhydride‐grafted PP (PP‐g‐MA) contents between 0 and 7 wt% are prepared. Increasing fiber contents enhance the Young's modulus and decrease the elongation at break and the notched impact strength. The tensile strength is barely affected. The addition of PP‐g‐MA increases the tensile strength as well as the elongation at break, whereas the Young's modulus is not influenced. Thus, PP‐g‐MA enhances the adhesion between PP and flax fibers significantly. POLYM. COMPOS., 36:2282–2290, 2015. © 2014 Society of Plastics Engineers     

MCC对PLA/PPC复合材料力学性能与热稳定性的影响

以微晶纤维素(MCC)作为改性剂,马来酸酐接枝聚乳酸(PLA g MAH)为界面相容剂,聚乳酸(PLA)、聚碳酸亚丙酯(PPC)为基体,通过熔融共混法制得PLA/PPC/MCC三元复合材料。采用控温拉伸、动态热分析、扫描电子显微镜以及热失重分析等方法研究了MCC对PLA/PPC的力学性能和热稳定性。结果表明,PLA/PPC/MCC三元复合材料的拉伸强度提高了12.7 %,玻璃化转变温度（Tg）提高了9.8 ℃;PLA g MAH的加入可以改善PLA/PPC/MCC三元复合材料的界面性质,从而提高力学性能和热稳定性;当PLA g MAH的添加量为5 %（质量分数,下同）时,三元复合材料在常温下的拉伸强度、弯曲强度和冲击强度分别提高了53.7 %、43.1 %和18.5 %;在60 ℃下三元复合材料的断裂强度提高了80 %;热降解温度以及最大失重温度与PLA/PPC相比分别提高了25.31 ℃和61.83 ℃。     

Water absorption and mechanical properties of PP/HIPS hybrid composites filled with wood flour

Water absorption and mechanical performance of the injection‐molded hybrid composites prepared from different ratios of two polymer blends (57 wt%), two compatibilizers (3 wt%), and two wood species (40 wt%) were investigated. The ratio of polypropylene and high‐impact polystyrene (HIPS) gradually increased in the blend (from 10 to 30 wt%). Styrene–ethylene–butylene–styreneblock copolymer and maleic anhydride‐grafted PP (MAPP) were used as compatibilizer (3 wt%). The shore D hardness of the PP/wood composites was improved by the incorporation of the HIPS. The HIPS/wood flour composites showed higher tensile modulus but lower tensile strength than the PP/wood composites. The water resistance of the PP/wood composites decreased with increasing HIPS content. POLYM. COMPOS., 38:863–869, 2017. © 2015 Society of Plastics Engineers     

Use of wet‐laid techniques to form flax‐polypropylene nonwovens as base substrates for eco‐friendly composites by using hot‐press molding

The wet‐laid process with flax (base) and polypropylene (binder) fibers has been used to obtain nonwovens for further processing by hot‐press molding. Mechanical characterization of nonwovens has revealed that slight anisotropy is obtained with the wet‐laid process as better tensile strength is obtained in the preferential deposition direction. The thermo‐bonding process provides good cohesion to nonwovens, which is critical for further handling/shaping by hot‐press molding. Flax:PP composites have been processed by stacking eight individual flax:PP nonwoven sheets and applying moderate temperature and pressure. As the amount of binder fiber is relatively low (<30 wt%) if compared with similar systems processed by extrusion and injection molding, it is possible to obtain eco‐friendly composites as the total content on natural fiber (flax) is higher than 70 wt%. Mechanical characterization of hot‐pressed flax:PP composites has revealed high dependency of tensile and flexural strength on the total amount of binder fiber as this component is responsible for flax fiber embedment which is a critical parameter to ensure good fiber–matrix interaction. Combination of wet‐laid techniques with hot‐press molding processes is interesting from both technical and environmental points of view as high natural fiber content composites with balanced properties can be obtained. POLYM. COMPOS., 2012. © 2011 Society of Plastics Engineers     

亚麻针刺毡/不饱和树脂复合材料的制备与研究

本文主要研究了亚麻纤维非织造物作为复合材料的增强体,采用真空辅助树脂传递模塑法(VARTM)与不饱和树脂复合成板材.最后对复合材料板材进行拉伸性能测试和力学性能比较.     

轴棒法C／C复合材料室温及高温拉伸性能研究

研究了轴棒法C／C复合材料在室温及高温下的轴向拉伸性能,并用扫描电镜观察了高温拉伸试样的断口形貌。结果表明,轴棒法C／C复合材料在室温及高温下的断裂模式不同,且高温下的拉伸强度高于室温下的拉伸强度;以常压炭化结束的C／C复合材料开孔率变大,室温及高温下的拉伸强度小于以高压炭化结束的C／C复合材料。     

ACETYLATED PLANT-FIBER-REINFORCED POLYESTER COMPOSITES: A STUDY OF MECHANICAL,HYGROTHERMAL, AND AGING CHARACTERISTICS

The potential of acetylation of plant fibers to improve the properties of composites was studied. The chemical modification of oil palm empty fruit bunch (EFB), coconut fiber (Coir), oil palm frond (OPF), jute, and flax using noncatalyzed acetic anhydride were investigated. Proof of acetylation was indicated by the increase in weight percent gain (WPG). Acetylation at a reaction temperature of 120°C had resulted in the reduction in the tensile properties (stress, modulus, and elongation at break) of EFB and Coir composites. However, at 100°C, the acetylated samples exhibited improved properties. The mechanical properties of acetylated EFB- and Coir-fiber-reinforced polyester composites was evaluated at different fiber loadings. The tensile strength and modulus were improved, but elongation at break was slightly reduced upon acetylation, particularly at high fiber loading. Impact properties were moderately increased for those composites with fiber loadings up to 45%. Acetylation exhibited a low moisture absorption, comparable with glass-fiber composites. Acetylated EFB and Coir composites showed superior retention of tensile and impact properties after aging in water up to 12 months.     

Injection Molding and Appearance of Cellulose-Reinforced Composites

Composite materials based on an ethylene-acrylic acid (EAA) copolymer and 20 wt% cellulose fibers were compounded by two runs in a twin-screw extruder. The composite material with cellulose fibers (CF) and a reference of unfilled EAA were injection molded into plaques using three different temperature profiles with end zone temperatures of 170°C, 200°C, and 230°C. The injection molded samples were then characterized in terms of their mechanical properties, thermal properties, appearance (color and gloss), and surface topography. The higher processing temperatures resulted in a clear discoloration of the composites, but there was no deterioration in the mechanical performance. The addition of cellulose typically gave a tensile modulus three times higher than that of the unfilled EAA, but the strength and strain at rupture were reduced when fibers were added. The processing temperature had no significant influence on the mechanical properties of the composites. Gloss measurements revealed negligible differences between the samples molded at the different melt temperatures but the surface smoothness was somewhat higher when the melt temperature was increased. In general, addition of the cellulose to the EAA reduced the gloss level and the surface smoothness. POLYM. ENG. SCI., 60:5–12, 2020. © 2019 Society of Plastics Engineers