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The optical, chemical and photochemical properties of organic molecules trapped in sol-gel materials for fiber optic chemical sensors.

机译:光纤化学传感器的溶胶-凝胶材料中捕获的有机分子的光学,化学和光化学特性。

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摘要

Effects of the sol-gel matrix on the optical properties of nile blue A, thionin and ruthenium(II)-tris(4,7-diphenyl-1,10-phenanthroline) were investigated. Three xerogel compositions doped with nile blue A and thionin were initially examined by absorption and fluorescence spectroscopy. The silicate and aluminosilicate xerogels exhibited similar spectral properties whereas the organically modified xerogels, synthesized from both tetraethyl orthosilicate (TEOS) and methyltrimethoxysilane (MTMS), shifted the absorbance and emission peaks towards the blue. The blue shift in the spectra was attributed to less polar xerogels that resulted from network modifying Si-CH{dollar}sb3{dollar} groups. Preliminary testing of the nile blue A and thionin containing xerogels for potential fiber optic sensor applications yielded negative results. The nile blue A xerogels, examined for pH sensing, were characterized by poor chemical stability in alkaline solutions. On the other hand, the photochemical properties of thionin prevented its use for hydrogen sulfide gas sensing.; The second part of experimentation evaluated the effect of MTMS on the properties of TEOS-derived xerogels. In thionin doped xerogels, increasing the concentration of MTMS was found to enhance the formation of thionin dimers. Secondly, FTIR spectroscopy revealed that MTMS additions reduced the polarity of the silica cage. Furthermore, atomic force microscopy (AFM) imaging of the xerogel surface exhibited surface roughening with the addition of MTMS.; The final stage of research instituted an organically modified silicate composition, doped with a ruthenium complex, that was coated onto a porous fiber substrate for fiber optic oxygen sensor measurements. Due to the reduced signal-to-noise ratio in the solid state instrumentation (a blue LED and a silicon detector), the ultimate sensitivity of this device was below 1 ppm. However, the sensor suffered from a relatively long response time of approximately 10 seconds and a poor Stern-Volmer ratio. Finally, preliminary results demonstrated a collimator device and a planar waveguide for oxygen sensor applications. The non-linear Stem-Volmer plots of these sensors were supported by a double exponential lifetime decay of the ruthenium complex that was trapped in the organically modified silicate composition.
机译:研究了溶胶-凝胶基质对尼罗蓝A,硫蛋白和钌(II)-三(4,7-二苯基-1,10-菲咯啉)光学性质的影响。首先通过吸收和荧光光谱检查了三种掺有尼罗蓝A和硫蛋白的干凝胶组合物。硅酸盐和铝硅酸盐干凝胶表现出相似的光谱特性,而由原硅酸四乙酯(TEOS)和甲基三甲氧基硅烷(MTMS)合成的有机改性干凝胶将吸收峰和发射峰移向蓝色。光谱中的蓝移归因于网络修饰Si-CH {dollar} sb3 {dollar}基团导致的极性较低的干凝胶。对潜在的光纤传感器应用的含尼罗河蓝A和硫蛋白的干凝胶的初步测试产生了负面结果。尼罗蓝A干燥凝胶经过pH感测,其特征是在碱性溶液中化学稳定性差。另一方面,硫蛋白的光化学性质阻止了其用于硫化氢气体感测。实验的第二部分评估了MTMS对TEOS衍生干凝胶性能的影响。在掺杂硫蛋白的干凝胶中,发现增加MTMS的浓度可增强硫蛋白二聚体的形成。其次,FTIR光谱表明添加MTMS可以降低二氧化硅笼的极性。此外,添加MTMS后,干凝胶表面的原子力显微镜(AFM)成像显示出表面粗糙。研究的最后阶段建立了一种有机改性的掺有钌配合物的硅酸盐组合物,该组合物被涂在多孔纤维基材上用于光纤氧传感器的测量。由于固态仪器(蓝色LED和硅探测器)的信噪比降低,因此该设备的最终灵敏度低于1 ppm。但是,该传感器的响应时间相对较长,约为10秒,并且斯特恩-沃尔默比很差。最后,初步结果证明了用于氧气传感器应用的准直仪设备和平面波导。这些传感器的非线性Stem-Volmer图得到了捕获在有机改性硅酸盐成分中的钌络合物的双指数寿命衰减的支持。

著录项

  • 作者

    Krihak, Michael K.;

  • 作者单位

    Rutgers The State University of New Jersey - New Brunswick.;

  • 授予单位 Rutgers The State University of New Jersey - New Brunswick.;
  • 学科 Engineering Materials Science.; Chemistry Analytical.; Physics Optics.
  • 学位 Ph.D.
  • 年度 1996
  • 页码 193 p.
  • 总页数 193
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;化学;光学;
  • 关键词

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