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限制在有机蒙脱石纳米级层间空间内的凝胶剂的自组装。

Self-assembly of gelators confined within the nano-scale interlayer space of organo-montmorillonite.

作者信息

Xiong Yun, Li Zifu, Feng Guilong, Wang Hong, Xu Huibi, Yang Xiangliang, Yang Yajiang

机构信息

School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

Phys Chem Chem Phys. 2008 Nov 21;10(43):6479-82. doi: 10.1039/b813525h. Epub 2008 Sep 25.

Abstract

The self-assembly of low molecular weight gelators confined within the nano-scale interlayer space of organo-montmorillonite is likely to be different from that under normal conditions (bulk space). Four kinds of gelators, 1-methyl-2,4-bis(N'-n-octadecylureido) benzene (MBB18), 1-methyl-2,4-bis(N'-n-dodecylureido)benzene (MBB12), bis(4'-stearamido phenyl) methane (BSM18) and bis(4'-octanamido phenyl)methane (BOM8), were used to investigate gelation of organic solvents confined within the nano-scale interlayer space of organo-montmorillonite. The possible morphologies of these gelators aggregates confined within the nano-scale space of organo-montmorillonite will be discussed in comparison with that in bulk space by employing differential scanning calorimetry (DSC) and X-ray diffraction (XRD). Herein, two types of organogels were prepared under the same conditions. One of them was formed within the interlayer space of organo-montmorillonite and another was formed in bulk space. The XRD patterns confirm that self-assembly of gelators takes place via an unusual pathway within the confined interlayer space of organo-montmorillonite, indicating that the alkyl chains of gelators adopt a parallel arrangement and do not insert into each other. This unusual arrangement of gelators confined within the interlayer space of organo-montmorillonite does lead to the different thermal effect observed by the DSC measurements. These features ultimately strengthen the thermodynamic stability of gelator aggregates, for example MBB18, and raise the gel-to-sol transition temperature, which jumps from 60 to 123 degrees C.

摘要

限制在有机蒙脱土纳米级层间空间内的低分子量凝胶剂的自组装可能与正常条件下(本体空间)不同。使用四种凝胶剂,1-甲基-2,4-双(N'-正十八烷基脲基)苯(MBB18)、1-甲基-2,4-双(N'-正十二烷基脲基)苯(MBB12)、双(4'-硬脂酰胺基苯基)甲烷(BSM18)和双(4'-辛酰胺基苯基)甲烷(BOM8),来研究限制在有机蒙脱土纳米级层间空间内的有机溶剂的凝胶化。通过差示扫描量热法(DSC)和X射线衍射(XRD),将与本体空间中的情况相比较,讨论这些限制在有机蒙脱土纳米级空间内的凝胶剂聚集体可能的形态。在此,在相同条件下制备了两种类型的有机凝胶。其中一种在有机蒙脱土的层间空间内形成,另一种在本体空间中形成。XRD图谱证实,凝胶剂在有机蒙脱土受限的层间空间内通过异常途径进行自组装,这表明凝胶剂的烷基链呈平行排列且不相互插入。这种限制在有机蒙脱土层间空间内的凝胶剂的异常排列确实导致了DSC测量中观察到的不同热效应。这些特征最终增强了凝胶剂聚集体(例如MBB18)的热力学稳定性,并提高了凝胶-溶胶转变温度,该温度从60℃跃升至123℃。

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