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61.
Hiroto Tachikawa Hiroshi Kawabata Kazumi Matsushige 《Journal of organometallic chemistry》2005,690(12):2895-2904
The structures and electronic states of phenyl-capped terthiophene (denoted by P3T) and the ionic species of P3T have been investigated by means of density functional theory (DFT) and direct MO dynamics calculations. P3T is one of the high-performance molecular devices, which has been utilized as a semi-conductor. The calculations indicated that the neutral P3T has a non-planar structure whose the phenyl rings in both ends of thiophene chain are largely deviated from the molecular plane. The cation and anion radicals, dication and dianion were considered as its ionic states. The structure for cation radical of P3T is close to more planar than that of neutral P3T. The structures for anion radical, dication and dianion take a pure planar structure. The first excitation energy of neutral P3T is calculated to be 2.90 eV at the TD-B3LYP/6-31G(d)//B3LYP/6-311+G(d) level, while the P3T cation and anion radicals have lower excitation energies (1.22 and 1.10 eV, respectively). The direct MO dynamics calculation showed that neutral, cation and anion hold near planar structure at 300 K. On the other hand, oligothiophene (n = 5) and its ionic species are strongly deformed from the planar structure, and thiophene rings in both ends of chain rotate rapidly by thermal activation. The mechanism of the electron conductivity in P3T was discussed on the basis of theoretical results. 相似文献
62.
The capacity for anaerobic decolorization of a sulfonated azo dye, Congo Red, by a strain of a sulfate-reducing bacterium
was evaluated. After optimizing the growth rate of the bacteria on a simple carbon source and terminal electron acceptor pair,
lactate and sulfate, respectively, the effect of the dye concentration on their growth rate was analyzed. The decolorization
rate was affected by the dye concentration in the growth medium. The azo-bond cleavage mechanism of reductive decolorization
with the formation of benzidine was consistent with the results, as this metabolite was identified by high-performance liquid
chromatography. Several fractions of the culture medium, including lysed cell extracts, were examined for the capacity to
reduce the azo dye. This reduction capacity was found in the culture medium in which the cells had previously grown. The results
showed that the mechanism of reductive decolorization of this sulfonated azo dye was extracellular and nonenzymatic, consistent
with the production of sulfide anion by the microorganisms while growing on lactate and sulfate. The sulfide anions were the
cause of the reduction leading to the disappearance of color in the medium. To increase the rate of decolorization, the presence
of ferrous ion was also necessary together with the lactate and sulfate substrates. 相似文献
63.
S. J. Pearton W. S. Hobson M. Geva U. K. Charkrabarti E. Lane A. P. Perley 《Plasma Chemistry and Plasma Processing》1991,11(2):295-310
The reactive ion etching of GaAs, InP, InGaAs, and InAlAs in CF3Br/Ar discharges was investigated as a function of both plasma power density (0.56-1.3 W - cm–2) and total pressure (10-40 mTorr) The etch rate of GaAs in 19CF3Br:1Ar discharges at 10 m Torr increases linearly with power density, from 600 Å min–1 at 0.56 W · cm–2, to 1550 Å · min at 1.3 W · cm–2. The in-based materials show linear increases in etch rates only for power densities above – 1.0 W · cm–2. These etch rates are comparable to those obtained with CCI2F2:O2 mixtures under the same conditions. Smooth surface morphologies and vertical sidewalls are obtained over a wide range of plasma parameters. Reductions in the near-surface carrier concentration in n-type GaAs are evident for etching with power densities of >0.8 W cm–2, due to the introduction of deep level trapping centers. At 1.3 W· cm–2, the Schottky barrier height of TiPtAu contacts on GaAs is reduced from 0.74 to 0.53 eV as a result of this damage, and the photoluminescent intensity from the material is degraded. Alter RIE, we detect the presence of both F and Br on the surface of all of the semiconductors. This contamination is worse than with CCl2F2-based mixtures. High-power etching with CF3Br/Ar together with Al-containing electrodes can lead to the presence of a substantial layer of aluminum oxide on the samples if the moisture content in the reactor is appreciable. 相似文献
64.
P. Goy 《International Journal of Infrared and Millimeter Waves》1982,3(2):221-234
This paper describes experimental results obtained with a packaged GaAs Schottky barrier diode in contact with a coaxial connector and placed across waveguides for bands Ka, V, E, W or F. Among the microwave sources used for calibration were 9 carcinotrons in the frequency interval 51–490 GHz. As soon as the frequency F is above the waveguide cut-off frequency, the different characteristics do not depend critically on the waveguide size for V, E, W and F bands. The video detection sensitivity, of several 100 mV/mW at 50 GHz and below, decreases as F–4 in the range 51–500 GHz. Coupling an X-band centimeter frequency via the coaxial connector and a millimeter frequency via the waveguide permits harmonic mixing in the diode. Between 36 and 490 GHz, the harmonic mixing number varies from 3 up to the very large value 40 with conversion losses from 18 to 88 dB. The minimum detectable signal in the 100 kHz band can be as low as –90 dBm at 80 GHz. A noticeable millimeter power is available at the waveguide output from injected centimeter power by harmonic generation. Starting for instance with 100 mW around 11.5 GHz, we have measured 0.1 mW at 80 GHz and 0.1 W at 230 GHz. To illustrate the possibility of creating usable millimeter and submillimeter wave without heavy equipment (such as carcinotrons or millimeter klystron) we report spectroscopic experiments in Rydberg atoms. Resonances have been observed up to 340 GHz by harmonic generation (28th harmonic) from an X-band klystron). 相似文献
65.
Summary Recently much attention has been directed to the validation of analytical methods. The level of validation will depend on the method application. If a method is developed for general use, for instance by different analysts, instruments or laboratories, then the effect of these changes need evaluation. This is normally referred to as ruggedness testing, where the limitations of the method to changes in the specified conditions are examined.This paper examines the use of Plackett-Burman fractional factorial experiment designs for ruggedness testing in high performance liquid chromatography (HPLC). The ability of these designs to identify confounding effects is applied to the stability indicating analysis of Salbutamol and its major degradation product, AH4045. The results show that confounding effects, proving extremely pertinent to HPLC, can be identified.The assay proved rugged to most tested changes although not to the use of column packing material from different manufacturers. 相似文献
66.
Ur?a?Opara?Kra?ovecEmail author Marko?Topi? Anneke?Georg Andreas?Georg Goran?Dra?i? 《Journal of Sol-Gel Science and Technology》2005,36(1):45-52
Nano-structured WO3-TiO2 layers were prepared by the sol-gel route. To obtain transparent, porous and crack free layers up to 0.8 μ m with a single dipping cycle a templating strategy was used. As a template three-dimensionally network based on organically modified silane was introduced to the WO3 and TiO2 sols. The WO3 layers were dip-coated onto the conductive glass substrate (TCO) and the TiO2 layers on the top of the WO3 layer. The morphology and the structure of the layers were determined by Scanning Electron Microscopy (SEM), High Resolution Transmission Electron Microscopy (HR-TEM), Energy Dispersive X-Ray Spectroscopy (EDXS), Auger and Infrared spectroscopy. SEM image of the WO3-TiO2 layer confirmed the nano-porosity of the layers and give the size of the particles of about 10 nm for TiO2 and 30 nm for WO3 layer. Further analysis indicated that the titanium sol penetrates the WO3 layer. Particles in the WO3 layer consist of a crystalline monoclinic WO3 core surrounded by a 5–10 nm amorphous phase consisting of WO3, TiO2 and SiO2. The WO3-TiO2 layers were used to assemble all solid state photoelectrochromic (PE) devices. Under 1 sun irradiation (1000 W/m2) the visible transmittance of the PE device changes from 62% to 1.6%. The colouring and bleaching processes last about 10 minutes. 相似文献
67.
68.
设计了开关控制实验,专门对常见的开关特点及使用进行探讨,根据开关特点搭建相应的控制电路,用近似于工程项目的形式锻炼学生对开关的灵活应用,激发了学生实验的兴趣和积极性. 相似文献
69.
M. Gamella S. Campuzano J. Manso G. González de Rivera F. López-Colino A.J. Reviejo J.M. Pingarrón 《Analytica chimica acta》2014
A non-invasive, passive and simple to use skin surface based sensing device for determining the blood's ethanol content (BAC) by monitoring transdermal alcohol concentration (TAC) is designed and developed. The proposed prototype is based on bienzyme amperometric composite biosensors that are sensitive to the variation of ethanol concentration. The prototype correlates, through previous calibration set-up, the amperometric signal generated from ethanol in sweat with its content in blood in a short period of time. The characteristics of this sensor device permit determination of the ethanol concentration in isolated and in continuous form, giving information of the BAC of a subject either in a given moment or its evolution during long periods of time (8 h). Moreover, as the measurements are performed in a biological fluid, the evaluated individual is not able to alter the result of the analysis. The maximum limit of ethanol in blood allowed by legislation is included within the linear range of the device (0.0005–0.6 g L−1). Moreover, the device shows higher sensitivity than the breathalyzers marketed at the moment, allowing the monitoring of the ethanol content in blood to be obtained just 5 min after ingestion of the alcoholic drink. The comparison of the obtained results using the proposed device in the analysis of 40 volunteers with those provided by the gas chromatographic reference method for determination of BAC pointed out that there were no significant differences between both methods. 相似文献
70.
Parawee Rattanakit Saisunee Liawruangrath 《International journal of environmental analytical chemistry》2013,93(7):739-754
A spectrophotometric microfluidic bioreactor system is described for the determination of organophosphorus pesticides. The glass chip was designed and fabricated for in situ monolithic preparation and subsequently acetlycholineserase (AChE) immobilization via a covalent bonding method. The porous polymer monolith was prepared using glycidyl methacrylate, ethylenedimethacrylate and 2,2-dimethoxy-1,2-diphenylethan-1-one in binary porogenic solvents of cyclohexanol and dodecanol. The epoxide groups of monolith were reacted with ethylenediamine and gluteraldehyde to allow immobilization of the enzyme using their amine groups. Organophosphorus pesticides can be determined by measuring their inhibition effect on the enzyme AChE using Ellman's reaction. A linear relationship between the absorbance and percentage inhibitions was obtained over the concentration range of 0.25 to 2.50?mg?L?1 paraoxon with a correlation coefficient (r 2) of 0.9974. The limit of detection (LOD) defined as 10% inhibition (I 10) was 0.17?mg?L?1 for paraoxon. The relative standard deviations (RSD) of 1.0?mg?L?1 paraoxon was 3.73% (n?=?5). The proposed µFI system incorporates efficient enzyme immobilization and reduces reagent consumption and waste production and could thus be considered to be more environmentally friendly. 相似文献