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1.
徐鸣  李忠明 《塑料工业》1998,26(5):25-26
本文采用烯基双酚A醚接枝低密度聚乙烯(LDPE-g-DBAE)作为高密度聚乙烯/聚碳酸酯(HDPE/PC)共混体系的增容剂,初步研究了LDPE-g-DBAE对HDPE/PC体系性能的影响。通过对共混物形态观察、耐热性能及力学性能测试,发现LDPE-g-DBAE对HDPE/PC体系有良好的增容效果;并发现了增容剂的最佳用量质量比大致为10%,提高增容剂的接枝率更有利于改善共混物的性能。65/35HDPE/PC共混物的HDT为92℃,拉伸强度302MPa,冲击强度298kJ/m2,分别比未加增容剂时的82℃,273MPa和155kJ/m2有较大提高。  相似文献   

2.
增容剂对HDPE/AS合金流变和力学性能的影响   总被引:2,自引:0,他引:2  
研究了增容剂氯化聚乙烯接枝(丙烯腈/苯乙烯)共聚物对HDPE/AS共混体系加工流变性能和力学性能的影响。增容剂使共混体系的塑化时间减少,且随着增容剂用量的增加,共混体系的平衡扭矩和拉伸强度增大,而断裂伸长率在HDPE/AS/PE-C-g-AS=80/20/4时出现极大值;螺杆转速的增加使共混体系的平衡扭矩增大。  相似文献   

3.
HDPE/PC共混体系的增容剂分子设计与合成   总被引:8,自引:1,他引:7  
介绍了高密度聚乙烯(HDPE)/聚碳酸酯(PC)共混体系的增容剂的分子设计与合成技术。采用了低密度聚乙烯(LDPE)在引发剂过氧化苯甲酰(BPO)存在下与二烯丙烯双酚A(DABPA)在二甲苯中进行溶液接枝共聚反应的工艺。通过重量法和X-射线光电子能谱(XPS)证实了接枝共聚物(LDPE-g-DABPA)的存在。研究了引发剂BPO用量、单体DABPA用量、反应时间及反应温度对接枝率的影响,确定了合成  相似文献   

4.
阻隔性HDPE/MPE/PA1010共混体系的研究   总被引:3,自引:0,他引:3  
用挤出法以马来酸酐(MAH)接枝高密度聚乙烯(HDPE)为增容剂(MPE),PA1010为阻隔组分,HDPE为基料,制取了HDPE/MPE/PA1010共混材料。研究了挤出温度、MPE用量、PA1010含量对其阻隔性能的影响,比较了几种不同渗透体系的吸油率和渗透损失量。  相似文献   

5.
阻隔改性组分PA6对HDPE/PA6合金性能的影响   总被引:5,自引:2,他引:3  
研究了HDPE/PA6合金阻隔改性组分PA6的筛选及其含量对该合金阻隔性能和力学性能的影响。结果表明,在增容剂的条件下,具有适当粘度的PA6能与HDPE共混制得宏观均匀的合金材料;PA6含量对共混体系的阻隔性能影响显著;当PA6占30份以上时,HDPE/PA6合金阻隔非极性溶剂的性能大幅度提高,同时,PA6的加入对合金有一定的增强作用。  相似文献   

6.
何慧  沈家瑞 《塑料工业》1998,26(6):28-30
通过扫描电镜照片(SEM)研究了HDPE/PET共混体系在双螺杆反应挤出过程中,共混合金冲击断面的形态特征。结果表明,增容剂EVA或EAA均对HDPE/PET共混体系具有一定的增容作用;使分散相颗粒减小,且变得较为均匀,两相界面变得模糊,界面粘结力增强。其中,EAA的增容效果优于EVA。在此增容的基础上,选用有机化合物D作为催化剂,在熔融加工的过程中,使PET与EVA或EAA发生酯交换或酸-酯交换反应,生成PET-EVA或PET-EAA接枝共聚物,达到了原位增容HDPE/PET共混体系的目的,从而进一步改善了体系的相容性,共混体系的力学性能也得到了有效的提高  相似文献   

7.
PC/HDPE共混材料的形态和性能   总被引:1,自引:0,他引:1  
选用燕经公司生产的HDPE对双酚P型聚碳酸酯(PC)进行改性,研究了PC/HDPE共混材料的微观形态,流变性能,及HDPE加入量对PC力学性能的影响,并对PC/HDPE材料的阻碍机理进行了初步探讨。  相似文献   

8.
PC/PET/PE-g-MAM三元共混体系流动性的研究   总被引:1,自引:0,他引:1  
以PEgMAH 和PEgMANa 、PEgMAZn 马来酸盐离聚物为相容剂组成PC/PET/PEgMAM 三元共混体系。用毛细管流变仪研究了不同PEgMAM 的接枝率及用量对共混物流动性的影响,结果表明:马来酸盐离聚物增强了PC 和PET 间的相容性,当其含量或接枝率较大时,可以显著降低PC/PET 共混物的表观粘度,提高体系的流动性,相同接枝率的PEgMANa 对共混体系表观粘度的影响更为显著。  相似文献   

9.
管蓉  鲁德平 《湖北化工》1997,14(3):16-18
对聚对本二甲酸乙二醇酯与高密度聚乙烯共混物近十几年来的研究进展进行了综述。PET与HDPE为不相容共混物,加入增容剂后,不仅增加了体系的相容性,而且改善了体系的性能。本文介绍了PET/HDPE共混体系的增容剂和性能。  相似文献   

10.
在HDPE/PET共混体系反应挤出原位增容的过程中,增容剂EVA,EAA侧基上的官能团与PET分子链上的酯基在有机金属化合物的催化下发生了酯交换反应,其作用机理存在差别:EVA与PET之间的相互作用主要生成PET/EVA接枝共聚物,而EAA与PET则主要生成共交联共聚物。  相似文献   

11.
烯基双酚A醚接枝LDPE对HDPE/PC相容性和结晶速率的影响   总被引:2,自引:1,他引:2  
本文通过热力学曲线,对HDPE/PC体系中HDPE的熔融温度(T_m)和PC的玻璃化转变温度(T_g)的测试,考察了增容剂烯基双酚A醚接枝LDPE(LDPE-g-DBAE)对共混体系相容性的影响,同时还研究了体系中HDPE的结晶速率。  相似文献   

12.
研究了乙烯-醋酸乙烯共聚物(EVA)增容高密度聚乙烯(HDPE)和聚碳酸酯(PC)共混体系,讨论了EVA,PC对HDPE/PC共混合金性能的影响。结果表明:随PC用量的增加,HDPE/PC共混合金的熔体流动速率减小,缺口冲击强度增大,拉伸强度增大,维卡软化点变化不大。EVA能够改善合金体系的加工流动性,却明显降低了合金体系的力学性能。  相似文献   

13.
The rheological behaviors of in situ microfibrillar blends, including a typical semicrystalline/semicrystalline (polyethylene terephthalate (PET)/high‐density polyethylene (HDPE)) and a typical amorphous/semicrystalline (polycarbonate (PC)/HDPE) polymer blend were investigated in this study. PET and PC microfibrils exhibit different influences on the rheological behaviors of microfibrillar blends. The viscosity of the microfibrillar blends increases with increased PET and PC concentrations. Surprisingly, the length/diameter ratio of the microfibrils as a result of the hot stretch ratio (HSR) has an opposite influence on the rheological behavior of the two microfibrillar blends. The stretched PET/HDPE blend exhibits higher viscosity than the unstretched counterpart, while the stretched PC/HDPE blend exhibits lower viscosity than the unstretched blend. The data obtained in this study will be helpful for constructing a technical foundation for the recycling and utilization of PET, PC, and HDPE waste mixtures by manufacturing microfibrillar blends in the future. POLYM. ENG. SCI., 45:1231–1238, 2005. © 2005 Society of Plastics Engineers  相似文献   

14.
A uniaxial tensile test was performed for polycarbonate (PC)/high‐density polyethylene (HDPE)/ethylene–vinyl acetate copolymer (EVA) blends with a fixed EVA content but various PC contents. The double‐yielding phenomenon and its composition dependence, as observed in the PC/HDPE blend, were again detected. EVA did not serve as a successful compatibilizer of PC and HDPE in the PC/HDPE/EVA blend. The incorporation of EVA resulted in a larger size and a more irregular shape of the PC fibers, as indicated in the scanning electron microscope observations; this, consequently, produced a higher serious stress concentration in the blend. This more complicated and instable morphology produced different double‐yielding behaviors in the PC/HDPE/EVA blends compared with the binary one. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008  相似文献   

15.
将高密度聚乙烯(HDPE)和聚碳酸酯(PC)在双螺杆挤出机中熔融共混挤出,通过改变对挤出物施加的牵引速度,研究了拉伸力场对HDPE/PC共混物的形态及其原位复合材料性能的影响。结果表明,随着牵引速度的提高,纤维状分散相所占比例增加,但纤维直径无明显变化;HDPE/PC原位复合材料与其普通共混材料相比,拉伸强度基本无变化,但冲击强度提高较大。  相似文献   

16.
研究了不同共混方式对高密度聚乙烯(HDPE)/聚碳酸酯(PC)共混体系形态与性能的影响。将不同组成的HDPE/PC分别在双螺杆、单螺杆挤出机中共混后注射成型,测试注射样条的力学性能并用扫描电子显微镜(SEM)对样条断面进行形态观察。结果发现,共混方式对共混体系拉伸强度影响不大,但对冲击强度和断面形态影响较大。当PC含量低时,双螺杆的共混效果不如单螺杆;当PC含量较高时,双螺杆的共混效果优于单螺杆。  相似文献   

17.
Summary: A fiber‐dependent double yielding phenomenon was recently observed in a structurally different blend, PC/HDPE, in which the first yield point is yielding of HDPE, and the second is caused by the yielding of injection‐induced PC fibers. The present study described the composition dependence of the double yielding in PC/HDPE blends with PC contents ranging from 0 to 45 wt.‐%. Morphology observation indicated that the injection‐molded PC/HDPE blends displayed a typical skin‐core structure with more or less injection‐induced elongated PC particles in the sub‐skin layers, and spherical PC particles in the core layers. Stress‐strain curves indicated that the blends with PC contents from 10 to 20 wt.‐% exhibit double yielding behavior and the cold drawing zone after the second yield point shortens with increasing PC content. The blends with too low‐ or too high‐PC contents exhibited only one yield point. Scanning electronic microscope micrographs of the blend with 15 wt.‐% PC showed that when the strain was beyond the first yield point the PC fibers notably yielded and even were broken, which served as an evidence that the yielding of PC phase was responsible for the second yielding. The origin of the composition dependence of the double yielding was discussed in detail through the interfacial stress transfer.

Representative stress‐strain curves for PE10, PE15, PE17.5, and PE20.  相似文献   


18.
系统研究了增容剂(LDPE-g-DABPA)对高密度聚乙烯(HDPE)/聚碳酸酯(PC)共混体系形态及拉伸性能、冲击性能、热性能、流动性能的影响,确定了增容剂的最佳用量。结果表明,在HDPE/PC/LDPE-g-DABPA为85/15/16时,体系拉伸强度没有变化,而冲击强度由未增容的13.86kJ/m增加到55.31kJ/m,提高了3倍,MFR由1.65g/10min增加到2.16g/10min,用裂纹扩展功(G1c)评价LDPE-g-DABPA的增容效果,结果表明,体系的G1c由增容前的0.0955J增加到0.2025J,说明LDPE-g-DABPA有良好的增容作用。  相似文献   

19.
Summary: Polycarbonate (PC)/high density polyethylene (HDPE) in situ microfibrillar blends were fabricated by a slit die extrusion, hot stretching, and quenching process. Despite PC and HDPE having a high viscosity ratio, which is usually disadvantageous to fibrillation, the morphological observation indicated that the blends had well‐defined PC microfibrils. The size and amount of the PC fibrils were nonuniform through the thickness of the extrudate, and were also affected by the PC concentration and hot stretch ratio. There were coarse and dense fibrils in the core zone, while these fibrils became finer and reduced in number toward the surface. The melt flow rate (MFR) of the PC/HDPE microfibrillar blend decreased with the increase of PC concentration, but increased with the larger hot stretching rate (or hot stretching ratio, HSR). Besides, it was found that the fibrillar blend had better flowability than the common blend with spherical particles at the same PC concentration. Temperature was also an important factor influencing the MFR due to the temperature dependence of PC and HDPE viscosity, and the PC phase morphology. The PC microfibrils could not be preserved beyond 230 °C and transformed into spherical particles. The rheological behaviors at various shear rates were studied by capillary rheometer. The orientation of PC fibrils and HDPE molecules with higher shear rate led to a decrease in the viscosity of microfibrillar blend. The data obtained in this study can help construct the technical foundation for recycling and utilization of PC and HDPE waste by manufacture of microfibrillar blends in future work.

SEM micrograph of the PC/HDPE microfibrillar blend.  相似文献   


20.
本文通过溶解试验和分析提取物,对PC/HDPE-g-MAH共混体系的微观结构、流变行为进行了研究。结果表明:在熔融共混过程中接枚于聚乙烯链上的羧酸或酸酐与聚磷酸酯发生了某种化学反应,在一定程度上改善了共混体系的相容性。  相似文献   

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