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81.
本非水电池体系由Li负极、多孔石墨电极和电解质溶液组成;电解质溶液由无机溶剂POCl_3(或有机溶剂硝基苯)和溶解在该溶剂中的活性物质(KIBr_2)及支持电解质构成。该电池体系的开路电压为8.50伏左右,放电性能良好,可望在实际中得到应用。此外,对电池体系的反应机理也作了初步的探讨。 相似文献
82.
用共振电离飞行时间质谱仪分析土壤中超痕量气态金 总被引:2,自引:0,他引:2
采用激光共振电离飞行时间质谱技术(简称RIS-TOF技术)对土壤中超痕量气态金的含量进行了分析研究。RIS-TOF谱仪具有极高的灵敏度和很强的选择性,避免了对样品的预富集过程。本文给出了该谱仪对金元素的检测限和65个土壤中气态金样品的分析结果,以及用中子活化法随机抽样检查的结果。 相似文献
83.
Yonghong Wen Zhi Qin Weisheng Liu 《Journal of Radioanalytical and Nuclear Chemistry》2001,250(2):285-289
The extraction of Am3+ and Eu3+ from aqueous picric acid solution by N, N-dinaphthyl-N, N-diphenyl-3,6-dioxaoctanediamide (LI) and 1, 1-(3, 6, 9-trioxaundecanedionyl)diphenothiazine (LII) was investigated by a radioactive tracer technique. Extraction distribution ratios of Am3+ and Eu3+ have been measured as a function of pH, picric acid concentration, extractant concentration, diluent and temperature. The extraction of Am3+ is preferred to that of Eu3+ for both LI and LII, and the latter gives larger separation factor than the former. The equilibrium constants and thermodynamic parameters of extraction reactions were also calculated. 相似文献
84.
微乳液介质—1—(2—吡啶偶氮)—2—萘酚光度法测定汽油中环烷酸铁的含量 总被引:8,自引:2,他引:8
本研究了微乳液为介质时,铁与1-(2-吡啶偶氮)-2-萘酚(PAN)的显色反应。选择730nm处为测定波长,ε为1.4×10^4L.mol^-^1.cm^-^1,铁量在0-50μg/25ml范围内符合比耳定律,该法适用于汽油中环烷酸铁的测定。 相似文献
85.
A facile one-step method has been developed for the synthesis of N-protected α-amino aldehyde acetals in moderate to good yields by three-component reaction of fluoroalkanesulfonyl azides, vinyl ethers and alcohol at 0 °C within 10 min. This practical synthetic method provides a convenient and expeditious access to N-per(poly)fluoroalkanesulfonyl α-amino aldehyde acetals. 相似文献
86.
A simple and efficient preparation of gramicidin S and its analogues is described. It involves solid-phase peptide synthesis and on-resin macrolactamization without side chain protection, affording cyclic products in high yield and high purity. The high specificity of the cyclization reaction was shown to originate in the formation of a pre-organized conformation of the linear biosynthetic precursor of gramicidin S. This facile method will provide convenient access to the analogues of the natural product for functional optimization to counter microbial resistance. 相似文献
87.
Ji QC Zhang J Rodila R Watson P El-Shourbagy T 《Rapid communications in mass spectrometry : RCM》2004,18(19):2293-2298
Quantitative determination of drug concentrations in tissue samples can provide critical information for drug metabolism, kinetics, and toxicity evaluations. For analysis of tissue samples using liquid chromatography/tandem mass spectrometric (LC/MS/MS) detection, homogenization is a critical step in achieving good assay performance. Assay performance can be closely evaluated by spiking the drug directly into tissue samples prior to homogenization. It is especially important to include this assay evaluation for the analysis of artery tissue samples because artery tissue is very elastic, making it quite a challenge to develop an effective procedure for homogenization. An LC/MS/MS assay in 96-well format using liquid-liquid extraction was developed for analyzing ABT-578 in rabbit artery samples. Tissue quality control samples were prepared by spiking ABT-578 stock solutions directly into the tissue before homogenization. The usage of the tissue control samples gives a thorough evaluation of the sample preparation process that includes both homogenization and sample extraction. A 20% blood in saline solution was used as a homogenization solution. Calibration standards were made by spiking ABT-578 into rabbit whole blood. Blood quality control samples were also prepared by spiking ABT-578 into rabbit whole blood. These blood QC samples were used to confirm the validity of the calibration curve. A lower limit of quantitation of 0.050 ng/mL was achieved. The linear dynamic range of blood standards was from 0.050-30.3 ng/mL with the correlation coefficient (r) ranging from 0.9969-0.9996. Overall %CV was between 1.3 and 7.0%, and analytical recovery was between 98.2 and 105.8% for blood QC samples. The %CVs for tissue QC samples were between 6.7 and 13.0%, and analytical recovery after correction was between 93.5 and 114.3%. 相似文献
88.
89.
90.
Xin Sheng Li Yan Xin Chen Yao Jun Zhang Chun Xin Ji Qin Xin 《Reaction Kinetics and Catalysis Letters》1996,58(2):391-396
Hydrogen adsorption-desorption over Mo2N has been studied using a temperature-programmed technique. It is revealed that hydrogen on Mo2N exhibits very high mobility leading to migration of the surface hydrogen into the sublayer and bulk of the sample or the reverse. The surface hydrogen species are preferentially formed when adsorption is carried out below 573 K. On increasing the adsorption temperature to above 573 K, the quantity of hydrogen species located in the sublayer or/and bulk of the Mo2N sample increases significantly. 相似文献