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11.
Summary Gas chromatography has been employed in the separation of mixtures of air, carbon dioxide, nitrous oxide and a volatile anaesthetic (halothane, isoflurane or enflurane) on a single Chromosorb 101 column by temperature programming from room temperature. Calibration over the required range for the analysis of exhaled air, demonstrated good linearity with a repeatability for test mixtures of about 1%. 相似文献
12.
Summary Six commercial hydrogen standards containing helium, oxygen, nitrogen, methane and carbon dioxide at trace levels were analyzed
by gas chromatography, for periods up to 105 days. The concentrations, in the range of 0–120 μmol mol−1, were stable (with the exception of oxygen) but often significantly different from the certified values provided by the suppliers,
especially for helium, oxygen and nitrogen. Concurrently, some experiments were carried out to verify the stability of gas
mixtures based on hydrogen stored in cylinders submitted to different chemical and physical treatments. The causes that led
to the deviations observed, as well as the decreases in oxygen, are discussed.
Presented at the 21st ISC held in Stuttgart, Germany, 15th–20th September, 1996. 相似文献
13.
Speed of sound and densities of the ternary mixture 2-propanol + diethyl ether + n-hexane and also the binary mixtures 2-propanol
+ diethyl ether and 2-propanol + n-hexane have been measured at the entire composition range at 298.15 K. The excess isentropic
compressibilities and the excess speed of the sound have been calculated from experimental densities and speed of sound. These
excess properties of the binary mixtures were fitted to Redlich-Kister equation, while the Cibulka’s equation was used to
fit the values related to the values to the ternary system. These excess properties have been used to discuss the presence
of significant interactions between the component molecules in the binary mixtures and also the ternary mixtures.
Speed of sound of the binary mixtures and the ternary mixture have been compared with calculated values from free length theory
(FLT), collision factor theory (CFT), Nomoto’s relation (NR), Van Deal’s ideal mixing relation (IMR) and Junjie’s relation
(JR). The results are used to compare the relative merits of these theories and relations in terms of the root mean square
deviation relative (RMSDr). 相似文献
14.
15.
The effect of CuO on the thermal behaviour of Zr/KClO4 primer mixtures was studied by thermoanalytical techniques, and the Bruceton method and its related calculation. It was found that the CuO catalytically promoted the decomposition of Zr/KClO4 primer mixtures and shifted the exothermic peak of DSC curves to lower temperatures. In addition, the Zr/KClO4 primer mixture containing CuO had a significant effect on the firing characteristics of electro-explosive devices. 相似文献
16.
In this review paper, the NBS scale and its limitations are briefly discussed. The magnitude of liquid junction potentials and some calculated values are presented. The use of a molality scale for hydrogen electrode concentration cells at high temperatures is described, and results from measurements on ionization equilibria are summarized. Use of this scale is also recommended for certain circumstances with cells without liquid junction. As an alternative activity scale, use of the Pitzer ion-interaction treatment for ions is recommended for special cases. Finally, reference data are presented for ±HCl in HCl(aq) to 350°C and (HCl+NaCl)(aq) to 200°C that were derived by use of the Pitzer ion-interaction treatment.Presented at the Second International Symposium on Chemistry in High Temperature Water, Provo, UT, August 1991. 相似文献
17.
Alessandro D' Aprano Dorina Ines Donato Antonio Carrubba Doctor in Chemistry thesis of A. Carrubba 《Journal of solution chemistry》1983,12(3):209-220
Conductance measurements are reported for LiPi, NaPi, KPi, RbPi, CsPi, Bu4NPi, Bu4NBr, Bu4NClO4, Bu4NNO3, and Bu4NBBu4 at 25°C in -butyrolactone-sulfolane mixtures. In these mixtures of solvents that are practically homomorphous, isodielectic and with comparable dipole moments, the ion pair association and ionic mobilities of large ions conform to the expectations of the primitive model. Electrolytes containing lithium or sodium ions show anomalies indicating that other factors besides shape, dipole moment, and polarizability of the solvent molecules are involved in the association and transport processes of these ions. 相似文献
18.
The polarographic behaviour of uranium and tellurium has been studied in the presence of increasing concentration of complex forming agent viz. ?-caprolactam at pH 4.4 for U(VI) and at pH 10.0 for Te(IV) at μ=0.1 M KNO3. In both cases the waves have been found to be diffusion controlled and irreversible. The values of kinetic parameters (σπa and K°f,h) have been calculated as a function of the ligand concentration. Method is suitable for the quantitative determination of these metals individually and simultaneously with the effect of diverse ions. 相似文献
19.
This is a sequel to Part I of A Subjective Bayesian Approach to the Theory of Queues. The focus here is on inference and a use of Shannon's measure of information for assessing the amount of information conveyed by the various types of data from queues. The notation and terminology used here is established in Part I. 相似文献
20.
Eugenio?Garcia-Pa?eda Pilar?Guardado Alfredo?MaestreEmail author 《Journal of solution chemistry》2004,33(10):1277-1293
Partial molar volumes at infinite dilution, V02, of alkali–metal halides (LiCl, NaCl KCl RbCl CsCl, NaBr, KBr, KI), tetra-n-alkylammonium bromides, R4NBr (R=Me, Et, n-Pr, n-Bu, n-Pen), NaBPh4, and Ph4PCl have been determined in binary solvent mixtures of water with 2-methyl-2-butanol covering the water-rich region and the alcohol-rich region at 298.15 K. V02 for alkali–metal halides show relatively little dependence on the solvent composition. However, in the case of hydrophobic electrolytes the observed effects are more pronounced. A good linear dependence between V02(R4NBr) and the molecular weight of the tetra-n-alkylammonium cation is found. Limiting single-ion volumes have been obtained using the assumption that V0(Ph4P+)–V0(BPh–4)=2.0 cm3-mol–1. The trends in the single-ion volumes are discussed in both solvent regions. 相似文献