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排序方式: 共有86条查询结果,搜索用时 640 毫秒
1.
Summary This paper reports the results of a study on the use of a new polymer-based, strong anion-exchange, stationary phase for rapid
and selective separation of carbohydrates and related compounds by high-pH, anion-exchange chromatography with pulsed amperometric
detection. The new adsorbent has been obtained by direct nitration of 2.8 μm, spherical non-porous highly cross-linked, styrene-divinylbenzene
copolymer beads, followed by reduction of superficially introduced nitro groups with nascent hydrogen and quaternization of
the resultant amino groups with iodomethane. It is reported that by optimizing the ionic strength of the mobile phase, columns
packed with the new anion-exchanger can be successfully employed to separate, either in isocratic or gradient elution mode,
oligosaccharides, positional isomers of gluco-disaccharides, as well as uronic acids and sugar monophosphates. 相似文献
2.
Toyohide Takeuchi Mototada Watanabe Tadashi Hamanaka Hiroki Haraguchi Daido Ishii 《Journal of separation science》1990,13(9):606-609
Capillary columns of 0.3-0.5 mm i.d. packed with 3- to 30-μm silica-based stationary phases for liquid chromatography were used for gas chromatographic separation of hydrocarbons. Column efficiencies were evaluated for various commercially available packing material. The best column efficiency was achieved with 5-μm octadecyl group bonded silica gel, the surface of which was coated with a poly (dimethylsiloxane) film. The 30-cm column produced 11,000 theoretical plates. 相似文献
3.
4.
An ion-exchange procedure is proposed for determination of Pt and Pd in environmental samples, using a Dowex 1-X10 anion-exchange resin. Pt and Pd were separated from the matrix elements in the sample by selective retention on the column as anionic chloro complexes and subsequent elution by circulated thiourea at 60 °C. The eluent, containing Pt and Pd was analyzed by inductively coupled plasma (ICP) atomic emission spectrometry (AES). Average recoveries of 98% and detection limit of 15 ng/g for both metals were achieved. Analysis of Pt and Pd concentrations in road dust, sampled from several sites in Germany was performed. The comparison of the obtained data with the concentrations of Pt and Pd in the same samples, determined by ICP-MS showed a very good agreement. 相似文献
5.
Summary The adsorption behaviour of 48 metal ions on DEAE-cellulose layers has been investigated in aqueous hydrobromic and hydriodic acid media. RF values are given as a function of the hydrobromic and hydriodic acid concentration over the ranges 0.01–6 mol dm–3 and 0.01–3 mol dm–3, respectively, and are compared with those obtained with Avicel SF. RF spectra are comparatively simple in both media, reflecting the strong affinity of the bromide and iodide ions to the DEAE-cellulose phase. Pd, Pt, Re, Au and Hg are distributed chromatographically in either system, while most other metal ions exhibit rather extreme RF values of near unity or zero. Therefore, the selectivity of the systems is particularly high for Pd, Pt, Re, Au and Hg, providing the possibility of their excellent selective separations. 相似文献
6.
Rodríguez-Cea A de la Campa MR Sanz-Medel A 《Analytical and bioanalytical chemistry》2005,381(2):388-393
Cytochromes P-450 are members of a superfamily of hemoproteins involved in the oxidative metabolism of various physiological and xenobiotic compounds in eukaryotes and prokaryotes. The multiplicity of this group of enzymes has been widely studied by chromatographic techniques, mainly high-performance liquid chromatography (HPLC). Because these enzymes are membrane-bound proteins, sample preparation for chromatographic separation of P-450 enzymes requires a solubilization step. The sample-preparation procedures are critical, because detergents affect not only the efficiency of protein solubilization but also their further chromatographic resolution. Trout liver microsomes have been taken here as a model sample to investigate iron speciation in cytochrome P-450. Trouts were treated intraperitoneally with -naphthoflavone, a potent inducer of some P-450 enzymes, and a microsomal suspension containing 7.4±0.1 nmol mL–1 P-450 enzymes was obtained by ultracentrifugation. Lubrol PX was selected as detergent for solubilization, resulting in about 90% solubilization recovery. The solubilized cytochromes P-450 were further separated by AE–FPLC, with UV detection, or coupled to ICP–MS with an octapole reaction system, ICP–(ORS)MS (monitoring Fe signals at masses 54, 56, and 57). A sampling procedure and chromatographic conditions are developed and were successfully applied to iron speciation in trout liver P-450 enzymes. ICP–(ORS)MS detection of P-450 enzymes is Fe-specific and so will give accurate information on the prosthetic group of the protein, which can constitute an advantageous alternative to classical methods for detection of these hemoproteins. 相似文献
7.
8.
Benjamin Ruiz Philippe Sistat Patrice Huguet Gérald Pourcelly Monica Araya-Farias Laurent Bazinet 《Journal of membrane science》2007
Electrodialysis (ED) is a membrane process used on a large scale. However, one of the common problems is fouling of ion-exchange membranes stacked in the cell. The use of pulsed power, consisting in applying a constant current density during a fixed time of application (Ton) followed by a pause duration (Toff), was demonstrated recently as an effective fouling mitigation method for electrodialysis. Up until now, no work has investigated the potential of electrodialysis using pulsed electric field on protein fouling. The aim of the present work was to study the influence of pulsed electric field (PEF) with a low frequency square shaped periodic signal (Ton = 10 s–Toff = 10 s, Ton = 10 s–Toff = 40 s) in comparison with dc current during electrodialysis of a casein solution at different current densities (10, 20 and 30 mA/cm2) on membrane fouling. It appeared from these results that PEF, under certain conditions of pulse, would avoid fouling on anion-exchange membranes. For 10 s–40 s pulsed electric field conditions, no fouling was observed with any density, while for 10 s–10 s PEF conditions, fouling appeared only at current density over 10 mA/cm2. dc current, whatever the current density conditions, led to a fouling on the diluate side of the AEM. Furthermore, when fouling occurred, magnitude layer thickness and dry weight increased with the applied current density. The nature of the fouling was identified as 97% protein. The protein fouling would be due to the dissociation of water molecules and/or heat increase at the anion-exchange membrane interface. The relaxation time of the pulse would limit both phenomena on the membrane. 相似文献
9.
F. Briski S. Cerjan-stefanovic L. Sipos 《International journal of environmental analytical chemistry》2013,93(1-4):137-148
Abstract The removal of ammonia from mineral medium containing known concentrations of ammonia (up to 300 mg/L) and from ground water by biological oxidation was studied. Nitrifying bacteria were isolated from ground water containing ammonia. Ammonium ion was determined by a standard titration technique while nitrite and nitrate ions were determined by ion chromatography (IC Supersep anion column) using 1.5 mM phtalic acid solution containing 5 % acetonitril as eluent. Depending on its concentration in water biooxidation of ammonia lasted from 48 hours till three weeks. 相似文献
10.
Chlorine isotope fractionation factor was determined by strongly basic anion-exchange chromatography with 0.1 mol/l HCl at 25 °C. The magnitude of the factor was calculated as a single-stage separation factor of 1.00030 with analytical precision of 0.00006 (1σ). The results showed that the lighter isotope () was preferentially fractionated into the resin phase, while the heavier one () enriched into the aqueous phase. This trend suggested that the hydrated Cl− ions in the aqueous phase were slightly more stable than the hydrated Cl− ions electrostatically interacting with the ion-exchange groups of the resin. 相似文献