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Separation of 23 dansylated amino acids by micellar electrokinetic chromatography at low temperature
Summary The baseline separation of 23 dansylated amino acids (including 3 didansylated species) is reported. Lowering of the analysis
temperature and fine control of the surfactant concentration were essential in obtaining this result. Calibration graphs with
good linearity were obtained. 相似文献
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A.F. Mesquita A.O. Porto G.M. de Lima J.M. Delgado F.S. Lameiras 《Solid State Communications》2005,136(3):133-137
Hexagonal and cubic cadmium selenide were prepared from a chemical route by using cadmium chloride and potassium selenium hydride obtained from reaction of selenium powder and potassium boron hydride. The product obtained was thermally treated under argon flux at 300, 500 and 600 °C for 2 h and characterized by X-ray photoelectron spectroscopy and X-ray diffraction. The X-ray diffraction data were refined by Rietveld method and the structural parameters were determined for the phases of each annealed samples. At 300 °C five phases were identified: Cubic and hexagonal cadmium selenides and the contaminants: Potassium chloride, boron oxide and cadmium boron oxide. At 500 and 600 °C only the hexagonal cadmium selenide phase was identified besides the other above mentioned contaminant. 相似文献
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J‐F. Masson Slaana Bundalo‐Perc Ana Delgado 《Journal of Polymer Science.Polymer Physics》2005,43(3):276-279
Differential scanning calorimetry (DSC) does not allow for easy determination of the glass‐transition temperature (Tg) of the polystyrene (PS) block in styrene–butadiene–styrene (SBS) block copolymers. Modulated DSC (MDSC), which deconvolutes the standard DSC signal into reversing and nonreversing signals, was used to determine the (Tg) of both the polybutadiene (PB) and PS blocks in SBS. The Tg of the PB block was sharp, at ?92 °C, but that for the PS blocks was extremely broad, from ?60 to 125 °C with a maximum at 68 °C because of blending with PB. PS blocks were found only to exist in a mixed PS–PB phase. This concurred with the results from dynamic mechanical analysis. Annealing did not allow for a segregation of the PS blocks into a pure phase, but allowed for the segregation of the mixed phase into two mixed phases, one that was PB‐rich and the other that was PS‐rich. It is concluded that three phases coexist in SBS: PB, PB‐rich, and PS‐rich phases. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 276–279, 2005 相似文献
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Given a vector measure ν with values in a Banach space X, we consider the space L1(ν) of real functions which are integrable with respect to ν. We prove that every order continuous Banach function space Y continuously contained in L1(ν) is generated via a certain positive map related to ν and defined on X* x M, where X* is the dual space of X and M the space of measurable functions. This procedure provides a way of defining Orlicz spaces with respect to the vector measure ν. 相似文献
8.
Tomás Chacón Rebollo Antonio Domı́nguez Delgado Enrique D. Fernández Nieto 《Comptes Rendus Mathematique》2004,338(1):85-90
In this work we introduce a class of balanced numerical schemes, up to second order, for the solution of general non-homogeneous hyperbolic systems of conservation laws. We give a general technique to build such schemes. We also prove that they balance up to second order a large class of steady solutions in the whole domain but some subset whose measure tends to zero as the grid size decreases to zero. We finally present an application to Shallow Water equations that exhibit the good performances of some of the schemes introduced. To cite this article: T. Chacón Rebollo et al., C. R. Acad. Sci. Paris, Ser. I 338 (2004). 相似文献
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E. Kajari R. Walser W. P. Schleich A. Delgado 《General Relativity and Gravitation》2004,36(10):2289-2316
We present exact expressions for the Sagnac effect of Gödel's Universe. For this purpose we first derive a formula for the Sagnac time delay along a circular path in the presence of an arbitrary stationary metric in cylindrical coordinates. We then apply this result to Gödel's metric for two different experimental situations: First, the light source and the detector are at rest relative to the matter generating the gravitational field. In this case we find an expression that is formally equivalent to the familiar nonrelativistic Sagnac time delay. Second, the light source and the detector are rotating relative to the matter. Here we show that for a special rotation rate of the detector the Sagnac time delay vanishes. Finally we propose a formulation of the Sagnac time delay in terms of invariant physical quantities. We show that this result is very close to the analogous formula of the Sagnac time delay of a rotating coordinate system in Minkowski spacetime. 相似文献
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Mary E. Neubert DAVID G. ABDALLAH Jr Sandra S. Keast Julie M. Kim Soonnam Lee Ryan M. Stayshich Margaret E. Walsh Rolfe G. Petschek Shin-Tson Wu 《Liquid crystals》2003,30(6):711-731
New diphenyldiacetylenes of the type with A, B = H and/or F; m = 0, 1; n = 1-4; and X = C n H 2n + 1 , F, CF 3 or CN were synthesized and their mesomorphic properties determined by hot stage polarizing microscopy and DSC. When m = 0, all of these compounds showed only a nematic phase except when X = CF 3 when both nematic and smectic A phases were seen. Both clearing and melting temperatures were higher than those reported for substitution with the corresponding alkyl chains but the much larger increase in clearing temperatures produced considerably wider nematic phases. Eutectic mixtures of a few of these olefins yielded nematic materials also having much wider temperature ranges and higher clearing temperatures than the eutectic mixtures of the alkyl compounds, while retaining their high birefringence and low viscosities. Such materials are of interest for beam-steering devices.
Four of the diacetylenes with m = 1 ( A, B = H) were also prepared ( X = C 6 H 13 , F, n = 2, 3). When X was C 6 H 13 ( n = 2), the nematic range was smaller in the 2- than in the 1-olefin but wider than in the alkyl series. When X = F, either no nematic phase or a monotropic one was observed, whereas the 1-olefins gave a much wider nematic phase. Both transition temperatures were lower than those for the corresponding 1-olefin and alkyl analogues. The compound with X = C 6 H 13 and n = 2 had a melting temperature below room temperature. 相似文献
Four of the diacetylenes with m = 1 ( A, B = H) were also prepared ( X = C 6 H 13 , F, n = 2, 3). When X was C 6 H 13 ( n = 2), the nematic range was smaller in the 2- than in the 1-olefin but wider than in the alkyl series. When X = F, either no nematic phase or a monotropic one was observed, whereas the 1-olefins gave a much wider nematic phase. Both transition temperatures were lower than those for the corresponding 1-olefin and alkyl analogues. The compound with X = C 6 H 13 and n = 2 had a melting temperature below room temperature. 相似文献