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101.
《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(13):3419-3419
102.
简要介绍便携式与固定式氧气探测报警器的区别及其在啤酒发酵储罐间的应用,列出了氧气探测报警器检定的主要技术指标。 相似文献
103.
Yan Shun MA Qing Hua MENG Hong Yu SHI Yuan De LONG Tian Bao HUANG 《中国化学快报》2006,17(6):807-808
Dencichine (β-N-oxalyl-L-α, β-diaminopropionic acid, L-ODAP), a nonprotein amino acid, is a haemostatic agent present in important Chinese medicinal herbs such as Panax notoginseng, as well as other Panax species1. It was first isolated from the seeds … 相似文献
104.
V. E. Kirichenko E. P. Promyshlennikova K. I. Pashkevich 《Russian Chemical Bulletin》1994,43(5):812-815
The dependence of the variations in the differential molar free energy of sorption of polyfluorocarboxamides RFC(O)NR2 (RF = CF3(CF2)
i
,i=0 to 5, R=H or Me) on capillary columns on the molecular structure of the amides, the temperature of analysis, and the nature of the stationary phases (OV-101, XE-60, and PEG-40M) were investigated by GLC. The peculiarities of the variation of the sorption characteristics of amides in XE-60 and PEG-40M polar phases, which cause the inversion of the order of retention of the members of pseudohomologous series, were found.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 868–871, May, 1994.We are grateful to R. V. Golovnya and D. N. Grigor'eva (Institute of Food Substances of the RAS, Moscow) for their participation in the discussion of the results obtained. 相似文献
105.
Flaked capillary columns with an OV-101/CE-Na{in3}PO{in4} hydrophobic-hydrophilic sorbent have been suggested. This sorbent provides for the analysis of polar and nonpolar substances, including amines and aminoalcohols, in aqueous and organic solvents. The efficiency of new columns was demonstrated for the analysis of 25 organic substances of various classes.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2169–2173, December, 1994.The work was financially supported by the Russian Foundation for Basic Research, Project No. 93-03-4969. 相似文献
106.
107.
K. Jaques W. Buda L. Dumortier J. Van der Eycken Arnold Venema Pat Sandra 《Journal of separation science》1994,17(2):72-73
Capillary GC on permethyl α-, β-, and γ-cyclodextrins has been applied to separate and quantify the enantiomers of some 2,3-iso-propylidene-1,2,3-cyclohexanetriol derivatives. Quantitative CGC data are compared to those obtained with chiral shift 1H NMR. 相似文献
108.
Fernando M. Lanas Janete H. Y. Vilegas Srgio Martins Elaine A. F. Gobato 《Journal of separation science》1994,17(4):237-244
An overview is presented of the analytical approaches developed by our research group over the last ten years for analysis of alternative fuel, both biomass and fossil. The alternative fuels are analyzed successively by PLC-8 (preparative liquid chromatography–group-type) fractionation and high resolution gas chromatography. Some of the possibilities for fractionation and characterization of alternative fuels are herein exemplified with sugar cane bagasse pyrolysis products. 相似文献
109.
A method has been developed to determine the boiling point distribution of sulfur compounds in light cycle oils (LCO'S). The method chosen for this analysis was GC with a flame photometric detector (FPD) and pyrolyzer. Tests were carried out to evaluate the recovery efficiency, repeatability, and accuracy of the method. Repeatabilities within 2% were obtained. The recovery of benzothiophenes and dibenzothiophenes was close to 100%; this was important because these are the major sulfur components in LCO's. No hydrocarbon or solvent interferences were observed with the use of the pyrolyzer, even for a 95% solvent level. Comparison with results from other techniques showed that the method accurately determined the levels of sulfur compounds in the LCO boiling point range. 相似文献
110.
Nitro musks in cosmetic products—determination by headspace solid-phase microextraction and gas chromatography with atomic-emission detection 总被引:1,自引:0,他引:1
Summary The combination of headspace solid-phase microextraction with atomic-emission detection enables highly selective and sensitive
determination of itro musk compounds in cosmetic products. Sample preparation is considerably simplified; there is no solvent
extraction step. Enrichment is influenced by the type and amount of cosmetic product investigated. The lowest amount giving
well detectable peaks is 1 mg musk compound per kg sample. Calibration curves obtained from spiked solutions of selected reference
cosmetics in water show very good linearity. Relative standard deviations of peak areas from repeated measurements are usually
<10%.
Presented at the 21st ISC held in Stuttgart, Germany, 15th–20th September, 1996 相似文献