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首页> 外文期刊>Iranian polymer journal >Modified preparation of HDPE/clay nanocomposite by in situ polymerization using a metallocene catalyst
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Modified preparation of HDPE/clay nanocomposite by in situ polymerization using a metallocene catalyst

机译:茂金属催化剂原位聚合改性制备HDPE /粘土纳米复合材料

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In this study, preparation of high-density polyethylene (HDPE)/clay nanocomposite by in situ polymerization of ethylene using a zirconocene catalyst (bis(cyclopentadienyl) zirconium dichloride (Cp2ZrCl2)) was investigated. To obtain higher efficiency, nanoclay particles (Na-montmorillonite) were modified by ammonia (NH3), NH3/methylaluminoxane (MAO), NH3/dodecylamine (DDA), and NH3/MAO/DDA systems. The results showed that the activity of the catalyst supported on the nanoclay particles modified by NH3/MAO (762 gp/mmol (Zr) t [atm]) was higher than that of the one supported on the unmodified nanoclay as well as the other prepared modified nanoclay-supported catalyst systems. The catalyst activities versus MAO concentration in NH3/MAO treatment system and versus DDA concentration in NH3/DDA system showed a maximum. Unexpectedly, a very low catalyst activity (180 gp/mmol(Zr) t [ atm]) was obtained using NH3/MAO/DDA system. X-ray diffraction patterns showed that the HDPE/clay nanocomposites prepared by NH3/MAO/DDA treatment system had less intercalated structure. Fourier transform infrared (FTIR) spectroscopy confirmed that water molecules of the nanoclay particles were reduced by NH3 modification. DSC results revealed that crystallinity of the HDPE/clay nanocomposites increased with the modification of the nanoclay particles. The maximum degree of crystallinity of 80.8% was obtained for HDPE/clay nanocomposites prepared by the nanoclay modified by NH3. In addition, nanoclay modification with NH3, NH3/MAO, and NH3/DDA systems resulted in higher thermal decomposition temperature (-30 degrees C higher than 480 degrees C of the unmodified one). Such increase was not observed for the -NH3/MAO/DDA treatment system. Dynamic mechanical analysis showed an increase in the elastic modulus of the nanocomposite samples prepared by modified nanoclay particles, as well. Meanwhile, modification of the nanoclay particles by NH3 led to the highest elastic behavior compared to the other modification systems. It was about 4.6 GPa which was 28% higher than the elastic modulus of the nanocomposite prepared by unmodified nanoclay particles.
机译:在这项研究中,研究了通过使用茂茂锆催化剂(双(环戊二烯基)二氯化锆(Cp2ZrCl2))原位聚合乙烯制备高密度聚乙烯(HDPE)/粘土纳米复合材料。为了获得更高的效率,通过氨水(NH3),NH3 /甲基铝氧烷(MAO),NH3 /十二烷基胺(DDA)和NH3 / MAO / DDA系统对纳米粘土颗粒(钠蒙脱土)进行了改性。结果表明,负载在NH3 / MAO改性的纳米粘土颗粒上的催化剂的活性(762 gp / mmol(Zr)t [atm])高于负载在未改性的纳米粘土上的催化剂的活性。改性的纳米粘土负载催化剂体系。催化剂活性相对于NH 3 / MAO处理系统中的MAO浓度和相对于NH 3 / DDA系统中的DDA浓度显示最大。出乎意料的是,使用NH3 / MAO / DDA系统获得了非常低的催化剂活性(180 gp / mmol(Zr)t [atm])。 X射线衍射图谱表明,NH3 / MAO / DDA处理系统制备的HDPE /粘土纳米复合材料的插层结构较少。傅里叶变换红外(FTIR)光谱证实,纳米粘土颗粒的水分子被NH3改性还原。 DSC结果表明,HDPE /粘土纳米复合材料的结晶度随纳米粘土颗粒的改性而增加。对于由NH 3改性的纳米粘土制备的HDPE /粘土纳米复合材料,最大结晶度为80.8%。此外,用NH3,NH3 / MAO和NH3 / DDA系统进行纳米粘土改性会导致较高的热分解温度(比未改性的480℃高-30℃)。对于-NH3 / MAO / DDA处理系统,未观察到这种增加。动态力学分析表明,改性纳米粘土颗粒制备的纳米复合材料样品的弹性模量也有所增加。同时,与其他改性体系相比,NH3对纳米粘土颗粒的改性导致最高的弹性行为。它约为4.6 GPa,比未改性的纳米粘土颗粒制备的纳米复合材料的弹性模量高28%。

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