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91.
The dinuclear copper(II) cryptate [Cu2L](ClO4)4 (1) cleaves the C-C bond of acetonitrile at room temperature to produce a cyanide bridged complex of [Cu2L(CN)](ClO4)3.2CH3CN.4H2O (2). The cleavage mechanism is presented on the basis of the results of the crystal structure of 2, electronic absorption spectra, ESI-MS spectroscopy, and GC spectra of 1, respectively. 相似文献
92.
The interaction of fluorocarbon containing hydrophobically modified polyelectrolyte(FMPAANa) with two kinds of nonionic surfactants(hydrogenated and fluorinated)in a semidilute (0.5wt%) aqueous solution had been studied by rheological measurements,Association behavior was found in both systems.The hydrophobic interaction of FMPAANa with fluorinated surfactant(FC171) is much stronger than that with hydrogenated surfactant(NP7.5) at low surfactoant concentrations.The interaction is strengthened by surfactants being added for the density of active junctions increased.Whereas distinct phenomena for FC171 and NP7.5 start to be found as the surfactants added over their respective certain concentration.The interaction of polyelectrolyte with fluorinated surfactant increases dramatical ly while that with hydrogenated surfactant decreases. 相似文献
93.
Zhang X Young MA Lyandres O Van Duyne RP 《Journal of the American Chemical Society》2005,127(12):4484-4489
A rapid detection protocol suitable for use by first-responders to detect anthrax spores using a low-cost, battery-powered, portable Raman spectrometer has been developed. Bacillus subtilis spores, harmless simulants for Bacillus anthracis, were studied using surface-enhanced Raman spectroscopy (SERS) on silver film over nanosphere (AgFON) substrates. Calcium dipicolinate (CaDPA), a biomarker for bacillus spores, was efficiently extracted by sonication in nitric acid and rapidly detected by SERS. AgFON surfaces optimized for 750 nm laser excitation have been fabricated and characterized by UV-vis diffuse reflectance spectroscopy and SERS. The SERS signal from extracted CaDPA was measured over the spore concentration range of 10(-14)-10(-12) M to determine the saturation binding capacity of the AgFON surface and to calculate the adsorption constant (Kspore=1.7 x 10(13) M(-1)). At present, an 11 min procedure is capable of achieving a limit of detection (LOD) of approximately 2.6 x 10(3) spores, below the anthrax infectious dose of 10(4) spores. The data presented herein also demonstrate that the shelf life of prefabricated AgFON substrates can be as long as 40 days prior to use. Finally, these sensing capabilities have been successfully transitioned from a laboratory spectrometer to a field-portable instrument. Using this technology, 10(4) bacillus spores were detected with a 5 s data acquisition period on a 1 month old AgFON substrate. The speed and sensitivity of this SERS sensor indicate that this technology can be used as a viable option for the field analysis of potentially harmful environmental samples. 相似文献
94.
Zhuang W. H. Gray D. Etemadi K. Benenson D. M. 《Plasma Chemistry and Plasma Processing》1995,16(1):S127-S139
Numerical modeling and experimental measurements have been performed to study the effects of powder carrier gas flow rates and powder sizes on the deposition offset in a plasma spray of yttria-stablized zirconia. The mathematical model involved simultaneous solution of the continuity, momentum and energy equations of the plasma gas, the dynamics and heat transfer of powder particles in the plasma, and the coupling effects between the plasma and panicles. Experiments included measurement of particle velocities by laser strobe technique and measurement of deposition offset. Calculated plasma temperatures and velocities are greater than 13,000 K and 2,000 m/s, respectively, in the vicinity of nozzle exit. For the plasma-particle momentum transfer, the drag coefficient was computed in two ways- with corrections accounting for the strongly varying plasma properties, and without these corrections. Calculated and experimental results, in respect to deposition offset, are in agreement to within 25% when calculated without varying properties corrections, and within about 40% with corrections; agreement in respect to average particle velocities is within 20% when calculated without varying properties corrections, and within the range 30–50% with corrections. 相似文献
95.
A novel approach to the detection of estriol using a flow injection system coupled to enhanced chemiluminescent immunoassay
was developed based on noncompetitive immunoassay formats. A conjugated estriol-ovalbumin immobilized immunoaffinity column
was inserted into the flow system to trap the unbound horseradish peroxidase (HRP)-labeled antibody after an off-line incubation
of estriol and HRP-labeled anti-estriol antibody. The trapped enzyme conjugate was detected by the injection of chemiluminescent
substrates to produce enhanced chemiluminescence. The linear range for the determination of estriol is 10.0 to 400 ng · mL−1 with a correlation coefficient of 0.996 and a detection limit of 5.0 ng · mL−1. The total time for sampling and chemiluminescent detection of one sample is 400 seconds after 30 min of pre-incubation.
The results for pregnancy serum samples obtained by this method are in good agreement with those obtained using ELISA. 相似文献
96.
Zhi-Yong Huang Zhi-Xia Zhuang Xiao-Ru Wang Frank S.C. Lee 《Analytica chimica acta》2004,508(2):239-245
Isotope dilution analysis method coupled with flow injection and inductively coupled plasma mass spectrometry (ID-FI-ICP-MS), enabled trace lead concentration in seawater to be determined and the high salt concentration in the matrix, such as Na+, Ca2+ and Mg2+, to be removed on-line. The operational parameters of the FI system including pH for the chelating reaction, concentration of 8-hydroxyquinoline-5-sulfonic acid (8-HQS), sample loading time and injection speed, washing time and speed, eluting acid concentration and eluting speed, and instrumental parameters for ICP-MS were optimized and selected. Accurate results could be achieved because the isotope ratios required can be precisely measured in the range of the eluting peak by means of ID-FI-ICP-MS. The 3σ detection limit was 0.204 ng ml−1. The trace lead concentration of seawater in south Xiamen, China was 0.988 ± 0.039 ng ml−1. The recoveries of spiked Pb standard in seawater and standard reference water (GBW 08607) were 97.9 and 101.0%, respectively, with a relative standard deviation of 0.98%. This method can be used to determine trace lead concentration in high salt matrix samples, and is especially useful when the eluting peaks do not have a Gaussian-distribution. 相似文献
97.
Zhixia Zhuang Chenglong Yang Xioaru Wang Pengyuan Yang Benli Huang 《Fresenius' Journal of Analytical Chemistry》1996,355(3-4):277-280
Palladium salts can be used as a coprecipitation carrier for the preconcentration of trace elements from natural water prior to their measurement by atomic spectrometry (AAS). The palladium is subsequently reduced by the introduction of hydrogen gas into the sample solution. The procedure is applied to the determination of Cu, Pb and Cd in seawater (enrichment factor 50) and synthetic water samples. Operating conditions have been optimized for the analysis of real samples. With the technique established an enrichment factor (500 fold) is feasible in synthetic samples. The recoveries of Cu, Cd and Pb from seawater are 95, 103 and 100%, respectively. This simple and rapid method can be applied in a wide pH-range and with complex matrices. 相似文献
98.
Guangdong Zhou Zhanlin Xu Xiaohong Guo Hong Zhuang Yanan Li Xueju Lü Tiexin Cheng Wenxing Li Kaiji Zhen 《Reaction Kinetics and Catalysis Letters》2005,85(1):57-64
Summary The oxidation of hexanol in the presence of the Keggin-type heteropoly compounds (HPCs) H3PMonW12-nO40 (denoted as PMonW12-n, n=0,1) and Na5PW11ZO39 (denoted as PW11Z, Z = Mn, Fe, Co, Ni, Cu and Zn) was carried out to produce hexanal and hexanoic acid. The reaction was conducted in tert-butanol (t-BuOH), using cetylpyridinium bromide (CPB) salts of HPA and 15% aqueous H2O2 as oxidant under mild condition. The PMoW11 catalyst showed higher hexanol conversion of 25%, the lowest selectivity to hexanal of 64.4% and an efficient utilization of H2O2 of 34%. Over the transition metal substituted PW11Z catalysts decomposition of H2O2 was rapid. For these PW11Z catalysts, the efficient utilization of H2O2 decreased to 9% or even lower. By means of IR, UV-visible and GC-MS techniques the catalysts were characterized. 相似文献
99.
合成了一种钴的酞菁配合物,以玻碳为基体、用化学吸附法制备了它的化学修饰电极。用CV法研究了该化学修饰电极对抗坏血酸氧化的电催化作用。结果表明,该化学修饰电极对抗坏血酸的氧化有一定的电催化作用,且电催化活性的稳定性高,抗坏血酸的电催化氧化峰电流和其浓度之间有良好的线性关系。 相似文献
100.