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101.
A new algorithm/program has been elaborated for simultaneous processing of different sets of vapour–liquid equilibrium data. The program was tested with six binary hexane + isomeric pentanol systems, each of them measured at three different isobaric conditions and one isothermal system of tert-butyl-methyl-ether + 2-methyl-2-propanol measured at three different temperatures. The correlation uses the maximum likelihood method, taking into account real behaviour of vapour phase. The parameters obtained are valid within the whole temperature range of the data, and are consistent in comparison with those obtained from individual correlations of isobars or isotherms. Results are presented for the Wilson and NRTL equations. 相似文献
102.
报道了FTS-20F富里叶红外光谱仪数据系统改造的工作采用IBM486计算机及新的数据接口取代了陈旧的NOVA4数据系统,文章详细描述了其硬件设计和软件编辑,改造不仅更新了FTS-20E里叶红外光谱仪,而且还使其达到90年代的水平。 相似文献
103.
104.
具有C2对称轴的手性配体及其不对称催化反应 总被引:2,自引:0,他引:2
按配位原子的数目进行分类,综述了近年来研究较多的具有C2对称轴的手性配体及其相关的不对称催化反应,并对该类手性配体的设计做了分析和总结。参考文献79篇。 相似文献
105.
M. Piñeiro-Iglesias M. Miñones-Vázquez E. Vázquez-Blanco S. Muniategui-Lorenzo P. López-Mahía D. Prada-Rodríguez 《Chromatographia》2002,56(7-8):483-488
Summary The aim of this work is to establish the best conditions for concentration and purification steps in the trace analysis of
aliphatic and polycyclic aromatic hydrocarbons (PAH) from atmospheric particulate matter by gas chromatography-flame ionisation
detection (GC-FID) and high performance liquid chromatography with ultraviolet and fluorescence detection (HPLC-UV-FL). The
best results for the more volatile compound were obtained with a combination of rotary evaporation and a stream of nitrogen
(near to 100% for aliphatic hydrocarbons and from 70 to 105% for PAH). Two types of solid phase extraction (SPE)cartridges
(Supelclean
tm
LC-Silica SPE tubes and Sep-Pak? Plus silica cartridges) and glass column were examined for the purification and fractionation step. Blank chromatograms of
both types of cartridges analysed by GC-FID made this study difficult, because a PSS (programmed split-splitless) injector
was employed thereby increasing the sensitivity. This problem was not observed in the HPLC-UV-FL blank chromatograms of these
cartridges. Glass columns filled with silica and alumina were chosen because no interference was found in the GC-FID blank
chromatograms and the best recoveries in the fractionation of both aliphatic hydrocarbons and PAH were achieved. This is especially
important when aliphatic hydrocarbons concentrations are lower than 1 μg mL−1. Finally, the selected conditions were applied to the analysis of hydrocarbons in real atmospheric particulate samples. 相似文献
106.
107.
The redox properties of the system Fe(tmphen)3(II/III) (tmphen=3,4,7,8-tetramethyl-1,10-phenanthroline) have been studied in the solvents nitromethane, acetonitrile, propanediol-1,2-carbonate, dimethylformamide, dimethylacetamide, dimethylsulfoxide and of the systems Fe(phen)3(II/III) (phen=1,10-phenanthroline) and Fe(niphen)3(II/III) (niphen=5-nitro-1,10-phenanthroline) in the solvents nitromethane, acetonitrile, propanediol-1,2-carbonate and acetone. The redox potentials of Fe(tmphen)3(II/III) are nearly independent of the solvent suggesting that the system might be used as a reference redox couple similar to the systems ferrocene/ferricinium or bisbiphenylchromium(0/I). In contrast the redox potentials of Fe(niphen)3(II/III) show a significant decrease with increasing donor number of the solvent which can be explained by nucleophilic attack of solvent molecules at the iron. It is shown that such a mechanism is consistent with the known solvent and salt effects on the kinetics of dissociation of ferroin and ferriin type complexes. 相似文献
108.
Ohne Zusammenfassung 相似文献
109.
110.
Kučinskaitė Agnė Pobłocka-Olech Loretta Krauze-Baranowska Mirosława Briedis Vitalis Savickas Aruñas Sznitowska Małgorzata 《平面色谱法杂志一现代薄层色谱法》2007,20(2):121-125
SPE and TLC have been used for qualitative and quantitative analysis of salidroside, rosavin, rosarin, and rosin in commercially available dry extracts from Rhodiola rosea roots. The best separation of all the compounds was achieved on silica gel TLC plates with ethyl acetate—methanol—water, 77 + 13 + 10 (v/v), as mobile phase. UV detection was performed at λ = 215 nm for salidroside and at λ= 245 nm for the rosavins (rosavin, rosarin, and rosin). Detection limits for salidroside and the rosavins were 90 ng and 60 ng per spot, respectively. Results from quantitative analysis confirmed the manufacturer’s declaration of the amounts of salidroside and the rosavins in the extracts.
相似文献