Benali Samira, Peeterbroeck Sophie, Larrieu Jeŕôme, Laffineur Fabrice, Pireaux Jean-Jacques, Alexandre Michaël, Dubois Philippe
Center of Innovation and Research in Materials and Polymers CIRMAP, Laboratory of Polymeric and Composite Materials, University of Mons-Hainaut, Académie Universitaire Wallonie-Bruxelles, Place du Parc 20, B-7000 Mons, Belgium.
J Nanosci Nanotechnol. 2008 Apr;8(4):1707-13.
The influence of the chemical structure of alkylammonium organo-modifying montmorillonite clays on the ability to form nanocomposites by melt blending, depending on the processing temperature and the organoclay thermal treatment, has been investigated. On one side chlorinated polyethylene/Cloisite 30B (nano)composite has been prepared by melt intercalation at 175 degrees C and its wide angle X-ray diffraction pattern revealed that the peak characteristic of the interlayer spacing of the organoclay was shifted to lower d-spacing, indicating a collapse of the organoclay structure. On the other side, (nano)composites based on ethylene-vinyl acetate copolymer/Cloisite 30B have been prepared by melt intercalation at 140 degrees C. At this temperature, exfoliation was observed with the as-received organoclay while the same organo-modified clay, simply dried at 180 degrees C for 2 hours, induced again the formation of a composite with a collapsed structure. The effect of the Cloisite 30B thermal treatment on the morphology and mechanical properties of ethylene-vinyl acetate-based (nano)composites was investigated using wide angle X-ray diffraction and tensile tests. In order to shed some light on the origin of this clay interlayer collapse, organoclay modified with various ammonium cations bearing long alkyl chains with different amounts of unsaturations were studied using wide angle X-ray diffraction and X-ray photoelectron spectroscopy before and after thermal treatment at 180 degrees C for 2 hours. Isothermal thermogravimetric analysis of all organoclays was also investigated. The layers collapse effect is discussed depending upon the level of unsatured hydrocarbon present in the organic surfactant.
研究了烷基铵有机改性蒙脱石粘土的化学结构对通过熔融共混形成纳米复合材料能力的影响,该影响取决于加工温度和有机粘土的热处理。一方面,通过在175℃下熔融插层制备了氯化聚乙烯/Cloisite 30B(纳米)复合材料,其广角X射线衍射图谱显示,有机粘土层间距的特征峰向较低的d间距移动,表明有机粘土结构发生了塌陷。另一方面,基于乙烯-醋酸乙烯酯共聚物/Cloisite 30B的(纳米)复合材料是在140℃下通过熔融插层制备的。在此温度下,使用原样的有机粘土观察到了剥离现象,而同样的有机改性粘土,仅在180℃下干燥2小时,再次诱导形成了具有塌陷结构的复合材料。使用广角X射线衍射和拉伸试验研究了Cloisite 30B热处理对乙烯-醋酸乙烯酯基(纳米)复合材料的形态和力学性能的影响。为了阐明这种粘土层间塌陷的起源,在180℃下热处理2小时之前和之后,使用广角X射线衍射和X射线光电子能谱研究了用带有不同不饱和量的长烷基链的各种铵阳离子改性的有机粘土。还研究了所有有机粘土的等温热重分析。根据有机表面活性剂中不饱和烃的含量讨论了层塌陷效应。