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DSC thermal analysis and X‐ray diffraction have been used to investigate the isothermal crystallization behavior and crystalline structure of nylon 6/clay nanocomposites. Nylon 6/clay has prepared by the intercalation of ε‐caprolactam and then exfoliating the layered silicates by subsequent polymerization. The DSC isothermal results reveal that introducing saponite into the nylon structure causes strongly heterogeneous nucleation induced change of the crystal growth process from a two‐dimensional crystal growth to a three dimensional spherulitic growth. But the crystal growth mechanism of nylon/montmorillonite nanocomposites is a mixed two‐dimensional and three‐dimensional spherulitic growth. The activation energy drastically decreases with the presence of 2.5 wt % clay in nylon/clay nanocomposites and then slightly increases with increasing clay content. The result indicates that the addition of clay into nylon induces the heterogeneous nucleation (a lower ΔE) at lower clay content and then reduces the transportation ability of polymer chains during crystallization processes at higher clay content (a higher ΔE). The correlation among crystallization kinetics, melting behavior, and crystalline structure of nylon/clay nanocomposites is also discussed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2196–2204, 2004 相似文献
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Heng Ding 《Polymer-Plastics Technology and Engineering》2020,59(8):809-821
ABSTRACTIn this article, a novel method, amidation, was used to modify saponite. Amidated ammonium citrate intercalated saponite (Aa-saponite) was synthesized by amidation reaction. The structure of Aa-saponite was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), demonstrating that the saponite was successfully amidated. Polylactic acid/amidated ammonium citrate intercalated saponite nanocomposites (PLA/Aa-saponite) were prepared by melt blending. Mechanical tests demonstrated that the addition of Aa-saponite (0.3 wt%) improved the impact strength of PLA. A series of performance analysis results showed that A-saponite improved the comprehensive performance of PLA, such as mechanical, thermal stability, crystallization and rheological properties. 相似文献
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合成皂石为前驱物制备高稳定性含镍介孔分子筛 总被引:4,自引:2,他引:2
以无机盐为原料通过控制pH值,用水热法合成含Ni皂石,并以此皂石为前驱物、十六烷基三甲基溴化铵为模板剂,制备含Ni介孔分子筛.用X射线粉末衍射、Fourier变换红外光谱、程序升温还原、透射电子显微镜、比表面积和孔径测定等仪器和方法表征样品的物化性能.结果表明:制得了有序性好的含Ni介孔分子筛,其比表面积为811.2m2/g,平均孔径为3.64nm.所制备的含Ni介孔分子筛经850℃焙烧3h或100℃水热处理10d后仍然具有介孔结构,说明样品具有高的(水)热稳定性. 相似文献
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Y. Kitayama T. Kodama M. Abe H. Shimotsuma Y. Matsuda 《Journal of Porous Materials》1998,5(2):121-126
The preparation of TiO2-pillared saponite was carried out in a CH3COOH aqueous solution. Titanium ion species to intercalate into the interlayer of saponite were obtained by an addition of Ti(C3H7O)4 to an aqueous solution of CH3COOH and by subsequent aging of the solution for a prescribed time. Ti4+-intercalated saponite including organic materials was obtained by ion exchange. After the sample was calcined at 500°C in air, TiO2-pillared saponite was obtained. The resulting TiO2-pillared saponite (Ti-Sapo) possessed surface areas in the range 300–400 m2/g and a sharp pore size distribution with the pore radius of 1.2 nm. The basal spacing of the product heated at temperature >250°C was about 2.45 nm. The pillar height of TiO2 in the Ti-Sapo was estimated to be 1.5 nm. 相似文献
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An iron-rich saponite, variety griffithite, from Griffith Park, California, USA, has been pillared with hydroxy-aluminium oligomers, giving rise to very crystalline layered solids with basal spacings of 17.4–17.7 Å and specific surface areas of 233–293 m2/g. The catalytic performance of these pillared solids, and also of the natural griffithite, all after calcination at 773 K, in the dehydrogenation of ethylbenzene was evaluated. The catalytic behaviour strongly depends on the acid properties developed in the solids by the pillaring treatment. 相似文献
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本文以水热合成法和共沉淀法制备了纳米Fe3O4/皂石复合材料,并用于去除水中2,4-二氯苯酚(2,4-DCP)。采用X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、扫描电镜(SEM)、透射电子显微镜(TEM)和X射线荧光光谱(XRF)等表征手段测试了纳米Fe3O4/皂石复合材料的物相组成、结构、形貌和元素组成,并考察了纳米Fe3O4/皂石复合材料在不同2,4-DCP溶液浓度、反应时间和pH等条件下对2,4-DCP的去除效果。结果表明,在皂石表面原位生长的纳米Fe3O4分散较为均匀,有效降低了Fe3O4的团聚现象。纳米Fe3O4/皂石复合材料在溶液pH值为6时,对2,4-DCP的最大去除量为178.46 mg/g,在反应时间为5 min时,对2,4-DCP去除量达到饱和。纳米Fe3O4/皂石复合材料对2,4-DCP的去除动力学符合准二级动力学模型。在此基础上,通过液相质谱联用(LC-MS)检测出2,4-DCP被降解后生成了氯酚等中间产物。本研究成果为水中有机污染物的降解提供了一种新型、环保且高效的环境功能材料。 相似文献