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Source Linke W. F. and Seidell A. Solubilities of Inorganic and Metal-Organic Compounds, American Chemical Society, Washington, DC, 1958, Vol. I, p. 1075. 

Zhang, X. Y., R. Arimoto, and Z. S. An, Dust Emission from Chinese Desert Sources Linked to Variations in Atmospheric Circulation, J. Geophys. Res., 102, 28041-28047 (1997). 

X-Ray Diffraction (XRD) patterns were recorded on a Philips HTK-KC diffractometer with a CuKa X-ray source, linked to Philips 386 computer. Thermo-Gravimetry (TG), was recorded on a Setaram TG-DTA 92 thermobalance. Diffuse Reflectance Spectra (DRS) were recorded on a Cary-5 spectrofotometer with a BaS04 integration-sphere in the UV-VIS-NIR region. Mossbauer spectra are recorded on a vertical constant acceleration drive in transmission geometry with a 28mCi Co(Rh) source. Isomer shift data are expressed relative to metallic Fe at 293 K which has an isomer shift of8 = -0.0888 mm/s relative to natural a-Fe. 

Figure 9.2 The basic components of a mass spectrometer. All mass spectrometers consist of an ion source linked to a mass analyser then to a detector. The important ion sources and mass analysers for biological mass spectrometry are listed. There are many other potential ion sources and mass analysers used generally in mass spectrometry, but only the indicated are of use in the analysis of biological macromolecules and amphiphilic lipids, and also in proteomics FAB fast atom bombardment MALDI matrix-assisted laser desorption and ionization ESI electrospray ionization ToF time of flight FTICR fourier transform ion cyclotron resonance MS/MS tandem mass spectrometry.

DART is easy to use and rapid. To release ions from the surface simply requires placing the samples in the flow of the excited gas atoms. As an example, there is an often heard rumor that U.S. doUar bills that have been in circulation will inevitably be contaminated with cocaine. One of the authors (J.G.) placed a 1 bill in a DART source linked to a time-of-flight analyzer. An ion was immediately observed that was within 5 ppm of tniz 304.1585 Da corresponding to the [M + H]+ of cocaine. 

Figure 4.2 Ragone plot describing various electrochemical power sources linked with present and future electric mobility options Source USABC PHEV Goals, US defense logistics agency, Product data sheets].

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