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Tuning cooperative vesicle templating and liquid crystal templating simply by varying silica source

机译:简单地通过改变二氧化硅源来调节协同囊泡模板和液晶模板

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摘要

The cooperative self-assembly of organic-inorganic siliceous composite structures has been studied from the aspect of inorganic precursors. We reveal that the vesicular or mesostructured materials can be obtained selectively by just changing the silica sources in one templating system. For poly(ethylene oxide)-type block copolymers with either poly (propylene oxide) or poly(butylene oxide) as the hydrophobic moieties, when the other synthesis parameters are exactly the same, the use of tetramethyl orthosilicate (TMOS) as a silica source gives rise to highly ordered mesostructures, while the use of tetraethyl orthosilicate (TEOS) leads to vesicles or foams. The attenuated total reflection Fourier transform infrared (ATR-FTIR) technique is used to monitor the silicate species derived from the hydrolysis and condensation of TMOS and TEOS as a function of the reaction time. On the basis of the ATR-FTIR results, we propose a "differentiating effect" at relatively high pH (4.7) to interpret the influence of different silica sources on the self-organized composite structures. For comparison, a "leveling effect" at relatively low pH (strong acidic conditions) is revealed to explain that both TMOS and TEOS lead to the same mesostructures. Our contribution provides a feasible and designable method to synthesize from conventional ordered mesostructures to novel vesicular structures, which are significant for their future practical applications.
机译:从无机前驱体的角度研究了有机-无机硅质复合结构的协同自组装。我们揭示了仅通过在一个模板系统中改变二氧化硅源就可以选择性地获得囊状或介孔结构的材料。对于以聚环氧丙烷或聚环氧丁烷为疏水部分的聚环氧乙烷型嵌段共聚物,当其他合成参数完全相同时,请使用原硅酸四甲酯(TMOS)作为二氧化硅源会产生高度有序的介孔结构,而原硅酸四乙酯(TEOS)的使用会导致囊泡或泡沫。衰减全反射傅里叶变换红外(ATR-FTIR)技术用于监测源自TMOS和TEOS水解和缩合的硅酸盐种类与反应时间的关系。根据ATR-FTIR结果,我们提出在较高pH(4.7)下的“差异作用”,以解释不同二氧化硅来源对自组织复合结构的影响。为了进行比较,揭示了在相对较低的pH(强酸性条件)下的“流平效果”,以解释TMOS和TEOS都导致相同的介观结构。我们的贡献为从常规的有序介观结构到新颖的囊泡结构的合成提供了一种可行且可设计的方法,这对它们的未来实际应用具有重要意义。

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  • 来源
    《Journal of Materials Research 》 |2010年第4期| p.648-657| 共10页
  • 作者单位

    Department of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    rnDepartment of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    rnDepartment of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    rnDepartment of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    rnDepartment of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    rnDepartment of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    rnDepartment of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    rnDepartment of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China Australian Research Council (ARC) Centre of Excellence for Functional Nanomaterials, and Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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  • 正文语种 eng
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