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171.
Susumu Yonezawa Shiori Nishibu Masayuki Takashima 《Journal of fluorine chemistry》2007,128(4):438-447
The preparation of the rare earth containing oxide fluoride glasses LnF3 (Ln; Y through Lu)-BaF2-AlF3-GeO2 in which the nominal content of LnF3 reached 60 mol% in maximum and their basic properties such as density, refractive index and glass transition temperature were investigated and summarized in detail. Especially, in order to discuss the local structure around the rare earth ion in the glass, the Judd-Ofelt analysis (discussion with Ω parameters) of the HoF3-BaF2-AlF3-GeO2 glasses was carried out. The unique fluorescent behavior and the magnetic properties of LnF3-BaF2-AlF3-GeO2 glasses (Ln = Tb and/or Sm) were also studied. 相似文献
172.
A new optical CO2 sensor based on the luminescence intensity change of the europium(III) complex tris(thenoyltrifluoroacetonato) europium(III) dihydrate ([Eu(tta)3]) caused by the absorption change of various pH indicators—thymol blue, phenol red, or cresol red—with CO2 was developed and its CO2 sensing properties were investigated. For all the CO2 sensors using pH indicators the observed luminescence intensity from [Eu(tta)3] at 613 nm increased with increasing CO2 concentration. The linear calibration method based on the plot of (I100–I0)/(I–I0) versus the inverse of CO2 concentration was suggested, where I0 and I100 were luminescence intensities at 613 nm of the CO2 sensor film in 100% nitrogen and 100% gaseous CO2. In all cases the plots showed good linearity and the correlation factors of the plots, r2, were 0.991 for thymol blue, 0.990 for phenol red, and 0.998 for cresol red. The slopes of the plots (A/B) for thymol blue, phenol red, and cresol red were 2.2, 5.2, and 9.0%, respectively. The response times of the CO2 sensor film were 4.0 s for thymol blue, 4.4 s for phenol red, and 8.8 s for cresol red for switching from nitrogen to CO2, and the recovery times of films were 36 s for thymol blue, 39.2 s for phenol red, and 56.6 s for cresol red for switching from CO2 to nitrogen. The signal changes were fully reversible and hysteresis was not observed during the measurements. The highly sensitive CO2 sensor was developed using thymol blue as an indicator for the CO2-sensing probe. 相似文献
173.
An optical CO2 sensor based on the overlay of the CO2 induced absorbance change of pH indicator dye α-naphtholphthalein in poly(isobutyl methacrylate) (polyIBM) layer with the fluorescence of tetraphenylporphyrin (TPP) in polystyrene layer is developed. The observed luminescence intensity from TPP at 655 nm increased with increasing the CO2 concentration. The ratio I100/I0 value of the sensing film consisting of α-naphtholphthalein in polyIBM and TPP in polystyrene layer, where I0 and I100 represent the detected luminescence intensities from a layer exposed to argon and CO2 saturated conditions, respectively, that the sensitivity of the sensor, is estimated to be 192. The response and recovery times of the sensing film are less than 6.0 s for switching from argon to CO2, and for switching from CO2 to argon. The signal changes are fully reversible and no hysterisis is observed during the measurements. The highly sensitive optical CO2 sensor based on fluorescence intensity changes of TPP due to the absorption change of α-naphtholphthalein in polyIBM layer with CO2 is achieved. 相似文献
174.
This paper introduces a mathematical model which makes it possible both to determine the concentration of photosynthetic herbicides and to obtain a quantitative parameter in order to compare their activity using a previously described sensing system. The working principle involves the changes in absorption properties at 860 nm of the reaction centre (RC) isolated from the bacteria Rhodobacter sphaeroides when photosynthetic herbicides are present. The method has been used for the determination and activity comparison of five photosynthetic herbicides: diuron, atrazine, terbutryn, terbuthylazine and simazine. Detection limits obtained were 2.2, 0.75, 0.046, 0.25, and 1.4 μM, respectively. The resulting order for the different herbicides according to their action on RC was: terbutryn > terbuthylazine > atrazine > simazine > diuron. 相似文献
175.
论述了激光拉曼光谱对高分子结构、结晶形态和表征,反应动力学过程和取向的研究,还介绍了纵向声学模、共振、高温高压、光波导和付里叶拉曼光谱在高分子研究中的最新进展。 相似文献
176.
177.
将高能Zn2+注入到CaF2介电基质中,在CaF2的表面下注入Zn2+浓度呈近似高斯分布,通过氧气氛后经热退火形成ZnO量子点.采用MaterialsStudio和Gaussian98W程序,结合实验结果计算分析了CaF2基质中ZnO纳米粒子的电子结构和光学性质.选取由4个ZnO原胞组成的超晶胞模型计算了ZnO纳米粒子的吸收光谱,理论结果与实验结果相符.对ZnO纳米粒子电子结构的研究结果表明,ZnO纳米粒子与CaF2基质的相互作用主要是ZnO表面的O与基质中Ca之间的作用,这种作用使ZnO纳米晶体的Fermi能级变窄,带隙相应减小;ZnO纳米粒子表面构型的变化对其本征吸收光谱没有影响,理论计算结果与实验值一致. 相似文献
178.
179.
Anilkumar Appajaiah Volker Wachtendorf Werner Daum 《Polymer Degradation and Stability》2006,91(11):2605-2613
The thermo-oxidative stability of commercially available polymer optical fibers (POFs) and their components (cores and claddings) was investigated. All the bare POFs (core and cladding only) studied here were based on poly(methyl methacrylate) (PMMA) core. The fibers were exposed to 100 °C/low humidity for about 4200 h. Chemiluminescence (CL) technique was applied to investigate the thermo-oxidative stability and for measuring the transmission loss during exposure a prototype device called multiplexer was used. POFs exhibited variation in thermo-oxidative stability although they possessed identical core material PMMA. This was due to difference in the chemical compositions of claddings. Claddings were more susceptible to the thermo-oxidative degradation compared to cores. The thermo-oxidative degradation of both the cladding and the core was found in POFs as a result of climatic exposure. POFs showed an early drop-off followed by a slow decline of transmission. The early drop-off of transmission was attributed to physical changes like thermal expansion and the slow decline of transmission to chemical changes like oxidative degradation of POFs. A good linear relationship between optical transmission stability and thermo-oxidative stability of POFs was established from these studies. 相似文献
180.
The plasma polymerization of 4-phenylbenzonitrile was carried out with the objective of synthesizing a novel conjugated polynitrile thin film with a better optical property. The structure, compositions and morphology of the plasma-polymerized 4-phenylbenzonitrile (PPBPCN) thin films were investigated by Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). A fine, homogenous PPBPCN film with a large π-conjugated system and a high retention of the aromatic ring structure of the starting monomer in the deposited plasma films is obtained when a low discharge power of 30 W was used during film formation. For the first time, a blue emission with relatively high photoluminescence intensity for PPBPCN thin films was observed. 相似文献