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Magnetic chromatography

Fig. 4. Multistage electromagnetic separator compared with a magnetic chromatography... Fig. 4. Multistage electromagnetic separator compared with a magnetic chromatography...
Takahashi, M. Fukui, S. Takahashi, Y. Abe, R. Ogawa, J. Yamaguchi, M. Sato, T. Imaizumi, H. Ohara, T. Numerical study on magnetic chromatography using quad-rupole magnetic field. IEEE Trans. Appl. Supercond. 2006, id (2), 1116-1119. [Pg.1428]

Ohara, T. Mori, S. Oda, Y. Wada, Y. Tsukamoto, O. Feasibihty of using magnetic chromatography for ultra-fine particle separation. Proc. lEE Japan 1995,161 166. [Pg.1428]

Ohara, T. Wang, X. Wada, H. Whitby, E.R. Magnetic chromatography Numerical analysis in the case of particle size distribution. Trans. IFF. Japan 2000,120-A (1), 62 7. [Pg.1428]

Microelectronics technologies are widely used to create new separators able to capture superfine and weakly magnetized particles. The on-chip made separators based on magnetic field-flow fractionation or magnetic chromatography can separate Brownian particles according to their magnetic properties and can be applied for analytical purposes.Apart from... [Pg.150]

The quadripolar spectrometers whose resolution is limited to about 2000 are of simpler design than the magnetic sectors and are less costly. They are often used in conjunction with gas chromatography (see section 3.3) for purposes of identification. [Pg.53]

To find explosives Gas analyzers, chromatography instruments, drift-spectrometers, neutron defectosopes, nuclear-magnetic and nuclear-quadrupole resonant instruments... [Pg.912]

Ring Currents Aromatic and Antiaromatic Magnetic Resonance Imaging Spectra by the Thousands Gas Chromatography GC/MS and MS/MS... [Pg.1329]

Both vapor-phase chromatography and high performance Hquid chromatography, along with nuclear magnetic resonance spectroscopy, have been used for isomer and composition analysis. [Pg.457]

Analytical methods iaclude thin-layer chromatography (69), gas chromatography (70), and specific methods for determining amine oxides ia detergeats (71) and foods (72). Nuclear magnetic resonance (73—75) and mass spectrometry (76) have also been used. A frequentiy used procedure for iadustrial amine oxides (77) iavolves titratioa with hydrochloric acid before and after conversion of the amine to the quaternary ammonium salt by reaction with methyl iodide. A simple, rapid quaHty control procedure has been developed for the deterrniaation of amine oxide and unreacted tertiary amine (78). [Pg.192]

Instmmental methods of analysis provide information about the specific composition and purity of the amines. QuaUtative information about the identity of the product (functional groups present) and quantitative analysis (amount of various components such as nitrile, amide, acid, and deterruination of unsaturation) can be obtained by infrared analysis. Gas chromatography (gc), with a Hquid phase of either Apiezon grease or Carbowax, and high performance Hquid chromatography (hplc), using siHca columns and solvent systems such as isooctane, methyl tert-huty ether, tetrahydrofuran, and methanol, are used for quantitative analysis of fatty amine mixtures. Nuclear magnetic resonance spectroscopy (nmr), both proton ( H) and carbon-13 ( C), which can be used for quaHtative and quantitative analysis, is an important method used to analyze fatty amines (8,81). [Pg.223]

The crystalline mineral silicates have been well characterized and their diversity of stmcture thoroughly presented (2). The stmctures of siHcate glasses and solutions can be investigated through potentiometric and dye adsorption studies, chemical derivatization and gas chromatography, and laser Raman, infrared (ftir), and Si Fourier transform nuclear magnetic resonance ( Si ft-nmr) spectroscopy. References 3—6 contain reviews of the general chemical and physical properties of siHcate materials. [Pg.3]

There are a variety of analytical methods commonly used for the characterization of neat soap and bar soaps. Many of these methods have been pubUshed as official methods by the American Oil Chemists Society (29). Additionally, many analysts choose United States Pharmacopoeia (USP), British Pharmacopoeia (BP), or Pood Chemical Codex (FCC) methods. These methods tend to be colorimetric, potentiometric, or titrametric procedures. However, a variety of instmmental techniques are also frequendy utilized, eg, gas chromatography, high performance Hquid chromatography, nuclear magnetic resonance spectroscopy, infrared spectroscopy, and mass spectrometry. [Pg.159]

When simple Hquids like naphtha are cracked, it may be possible to determine the feed components by gas chromatography combined with mass spectrometry (gc/ms) (30). However, when gas oil is cracked, complete analysis of the feed may not be possible. Therefore, some simple definitions are used to characterize the feed. When available, paraffins, olefins, naphthenes, and aromatics (PONA) content serves as a key property. When PONA is not available, the Bureau of Mines Correlation Index (BMCI) is used. Other properties like specific gravity, ASTM distillation, viscosity, refractive index. Conradson Carbon, and Bromine Number are also used to characterize the feed. In recent years even nuclear magnetic resonance spectroscopy has been... [Pg.434]

Composition The law of mass aclion is expressed as a rate in terms of chemical compositions of the participants, so ultimately the variation of composition with time must be found. The composition is determined in terms of a property that is measured by some instrument and cahbrated in terms of composition. Among the measures that have been used are titration, pressure, refractive index, density, chromatography, spectrometry, polarimetry, conduclimetry, absorbance, and magnetic resonance. In some cases the composition may vary linearly with the observed property, but in every case a calibration is needed. Before kinetic analysis is undertaken, the data are converted to composition as a function of time (C, t), or to composition and temperature as functions of time (C, T, t). In a steady CSTR the rate is observed as a function of residence time. [Pg.707]

Identification of stmctures of toxic chemicals in environmental samples requires to use modern analytical methods, such as gas chromatography (GC) with element selective detectors (NPD, FPD, AED), capillary electrophoresis (CE) for screening purposes, gas chromatography/mass-spectrometry (GC/MS), gas chromatography / Fourier transform infra red spectrometry (GC/FTIR), nucleai magnetic resonance (NMR), etc. [Pg.416]


See other pages where Magnetic chromatography is mentioned: [Pg.933]    [Pg.969]    [Pg.150]    [Pg.1428]    [Pg.1428]    [Pg.897]    [Pg.899]    [Pg.933]    [Pg.969]    [Pg.150]    [Pg.1428]    [Pg.1428]    [Pg.897]    [Pg.899]    [Pg.34]    [Pg.242]    [Pg.402]    [Pg.434]    [Pg.445]    [Pg.5]    [Pg.138]    [Pg.33]    [Pg.140]    [Pg.542]    [Pg.84]    [Pg.340]    [Pg.148]    [Pg.393]    [Pg.395]    [Pg.535]    [Pg.196]    [Pg.317]    [Pg.366]    [Pg.106]    [Pg.387]    [Pg.52]   
See also in sourсe #XX -- [ Pg.933 ]




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