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51.
52.
The ion-pair generation rate (ionization topography) in plasmas from63Ni and particularly Ti3H4 foils, as used in electron capture detectors, was measured at room temperature using large, parallel plates of low backscattering ability in nitrogen gas of varying density. For one atmosphere pressure, the fall-off of ion pair formation as calculated from the exponential region equalsN
0·e
–0.19d
for63Ni andN
0·e
–1.4d
for3H (whereN
0 is the initial ionization rate immediately adjacent to the foil andd is the distance from the foil in mm). The experimentally measured half ranges (distances from the foil within which 50% of all possible ion pairs are created) are 2.7 mm for63Ni and 0.27 mm for3H. The half ranges calculated from the exponential region where there is less interference from electron backscattering, are 3.7 and 0.5 mm, respectively. The latter values are considered closer to the true, unimpeded ionization topography near planar63Ni and3H foils.Material taken from doctoral thesis 相似文献
53.
Substituted norbornenes and dibenzobarrelene react under forced conditions with -methyl-1,2,4-triazolin-3,5-diones to afford urazoles via (2+2)-cycloaddition. 相似文献
54.
Ronald G. Sutherland Adam Pirko Udai S. Gill Choi Chuck Lee 《Journal of heterocyclic chemistry》1982,19(4):801-803
A method for the synthesis of heterocylic systems related to 9,10-dihydroanthracene with two hetero-atoms at the 9,10-positions is described. It involves the nucleophilic substitution reaction of η6-o-dichlorobenzene-η5-cyclopentadienyliron hexafluorophosphate with two nucleophilic groups (OH, SH and/or NH2) located in the 1,2-positions of a benzene ring to give a cyclopentadienyliron complexed heterocycle. Upon pyrolytic sublimation of the complex, the free heterocyclic compound is then obtained. 相似文献
55.
M. Arnold J. Kowalski G. zu Putlitz T. Stehlin F. Träger 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1986,3(2):329-333
The fragmentation of sulphur clusters caused by electron impact ionization was studied. For this purpose, a beam ofS n -clusters withn≦8 was generated in a gas aggregation source and ionized by electrons of variable energy. Special care was taken to maintain constant nucleation conditions so that the neutral cluster composition remained unchanged. It was found that the cluster ion mass spectra drastically depend on the electron energy. Even near threshold fragmentation processes contribute significantly to the dependence of the ion intensities on the electron energy. 相似文献
56.
A new method for successive determination of calcium and magnesium is proposed. It is based on the indirect determination of calcium in borax media by back-titration of excess of EGTA with lead nitrate. Magnesium is then determined in ammonia buffer with DCTA. For both titrations Thymolphthalexone is used as indicator. The exceptional role of DCTA in direct titration of magnesium is established experimentally and explained. 相似文献
57.
Simultaneous measurement of glucose and glutamine in aqueous solutions by near infrared spectroscopy 总被引:1,自引:0,他引:1
Hoeil Chung Mark A. Arnold Martin Rhiel David W. Murhammer 《Applied biochemistry and biotechnology》1995,50(2):109-125
A method is described for measuring the concentrations of both glucose and glutamine in binary mixtures from near infrared
(NIR) absorption spectra. Spectra are collected over the range from 5000–4000/cm (2.0–2.5μm) with a 1-mm optical path length.
Glucose absorbance features at 4710, 4400, and 4300/cm and glutamine features at 4700, 4580, and 4390/cm provide the analytical
information required for the measurement. Multivariate calibration models are generated by using partial least squares (PLS)
regression alone and PLS regression combined with a preprocessing digital Fourier filtering step. The ideal number of PLS
factors and spectral range are identified separately for each analyte. In addition, the optimum Fourier filter parameters
are established for both compounds. The best overall analytical performance is obtained by combining Fourier filtering and
PLS regression. Glucose measurements are established over the concentration range from 1.66–59.91 mM, with a standard error of prediction (SEP) of 0.32 mM and a mean percent error of 1.84%. Glutamine can be measured over the
concentration range from 1.10–30.65 mM with a SEP of 0.75 mM and a mean percent error of 6.67%. These results demonstrate
the analytical utility of NIR spectroscopy for monitoring glucose and glutamine levels in mammalian and insect cell cultures. 相似文献
58.
This paper characterizes the conditions required to form nanoliter-sized droplets (plugs) of viscous aqueous reagents in flows of immiscible carrier fluid within microfluidic channels. For both non-viscous (viscosity of 2.0 mPa s) and viscous (viscosity of 18 mPa s) aqueous solutions, plugs formed reliably in a flow of water-immiscible carrier fluid for Capillary number less than 0.01, although plugs were able to form at higher Capillary numbers at lower ratios of the aqueous phase flow rate to the flow rate of the carrier fluid (in all the experiments performed, the Reynolds number was less than 1). The paper also shows that combining viscous and non-viscous reagents can enhance mixing in droplets moving through straight microchannels by providing a nearly ideal initial distribution of reagents within each droplet. The study should facilitate the use of this droplet-based microfluidic platform for investigation of protein crystallization, kinetics, and assays. 相似文献
59.
Conditions for converting a set of five standard proteins to electrochemically active sodium dodecylsulfate (SDS) complexes were worked out with the aim of using such complexes for conductivity detection with a a chip electrophoresis system. The results obtained were compared with standard capillary electrophoresis (37 cm (effective length 30 cm)×75 μm I.D. capillary, 10 kV, negative polarity at the inlet). The chip separations were run at 500 V per chip (100 V/cm) as compared to the standard capillary arrangement, which was run at 266.6 V/cm. For the capillary set-up the protein complexes were prepared in aqueous solution (Milli-Q water) made 10 mM with respect to SDS. If the SDS concentration was increased to 50 mM, the separation in the capillary was incomplete. On the other hand with the chip system both approaches yielded acceptable results. The chip separations were slightly (but not distinctly) shorter and offered better separations than the standard set-up. The concentration of the surfactant used for the preparation the complexes results in alternations of the elution sequence, which is preserved if the chip separation is used instead of the capillary set-up. Apparently the full capacity of protein–SDS binding is not exploited for the preparation of the adducts. 相似文献
60.
The isolation and amino acid sequence of substance P from horse intestine is reported. The sequence, H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2 is identical with the sequence reported for substance P isolated from bovine hypothalami. 相似文献