Mass spectrometry design

Milgram, K. E. Abatement of spectral interferences in elemental mass spectrometry design and construction of inductively coupled plasma ion sources for Fourier Transform ion cyclotron resonance instrumentation, Ph. D. Thesis, University of Florida, 1997, Diss. Abstr. Int., B 1998, 59(2), 639. 

M. A. Moseley, L. J. Deterding, K. B. Tomer, and J. W. Jorgenson, Capillary-zone electrophoresis/fast-atom bombardment mass spectrometry design of an on-line coaxial continuous-flow interface. Rapid Commun. Mass Spectrom. 3, 87-93 (1989). 

J.L, and Costello, C.E. (2004) A high pressure matrix-assisted laser desorption ion source for Fourier transform mass spectrometry designed to accommodate large targets with diverse surfaces. J. 

O Connor, RB., Budnik, B.A., Ivleva, V.B., Kaur, P., Moyer, S.C., Pittman, J.L., and Costello, CE. 2004. A high-pressure matrix-assisted laser desorption ion source for Fourier transform mass spectrometry designed to accommodate large targets with diverse surfaces, /. Am. Soc. Mass Spectrom., 15 128-32. 

Following the movement of airborne pollutants requires a natural or artificial tracer (a species specific to the source of the airborne pollutants) that can be experimentally measured at sites distant from the source. Limitations placed on the tracer, therefore, governed the design of the experimental procedure. These limitations included cost, the need to detect small quantities of the tracer, and the absence of the tracer from other natural sources. In addition, aerosols are emitted from high-temperature combustion sources that produce an abundance of very reactive species. The tracer, therefore, had to be both thermally and chemically stable. On the basis of these criteria, rare earth isotopes, such as those of Nd, were selected as tracers. The choice of tracer, in turn, dictated the analytical method (thermal ionization mass spectrometry, or TIMS) for measuring the isotopic abundances of... 

To examine a sample by inductively coupled plasma mass spectrometry (ICP/MS) or inductively coupled plasma atomic-emission spectroscopy (ICP/AES) the sample must be transported into the flame of a plasma torch. Once in the flame, sample molecules are literally ripped apart to form ions of their constituent elements. These fragmentation and ionization processes are described in Chapters 6 and 14. To introduce samples into the center of the (plasma) flame, they must be transported there as gases, as finely dispersed droplets of a solution, or as fine particulate matter. The various methods of sample introduction are described here in three parts — A, B, and C Chapters 15, 16, and 17 — to cover gases, solutions (liquids), and solids. Some types of sample inlets are multipurpose and can be used with gases and liquids or with liquids and solids, but others have been designed specifically for only one kind of analysis. However, the principles governing the operation of inlet systems fall into a small number of categories. This chapter discusses specifically substances that are normally liquids at ambient temperatures. This sort of inlet is the commonest in analytical work. 

The term nebulizer is used generally as a description for any spraying device, such as the hair spray mentioned above. It is normally applied to any means of forming an aerosol spray in which a volume of liquid is broken into a mist of vapor and small droplets and possibly even solid matter. There is a variety of nebulizer designs for transporting a solution of analyte in droplet form to a plasma torch in ICP/MS and to the inlet/ionization sources used in electrospray and mass spectrometry (ES/MS) and atmospheric-pressure chemical ionization and mass spectrometry (APCI/MS). 

Gas Chromatography and Mass Spectrometry A Practical Guide is designed to be a valuable resource to the GC/MS user by incorporating much of the practical information necessary for successful GC/MS operation into a single source. With this purpose in mind, the authors have kept the reading material practical and as brief as possible. This guide should be immediately valuable to the novice, as well as to the experienced GC/MS user who may not have the breadth of experience covered in this book. 

The preparative reactions were conducted in sealed tubes in which — 1-3 g of the reagents had been placed. After the vessels had been maintained at the indicated temperatures for the designated times, the contents were removed, to be separated by fractional condensation and GLC. In addition to the (trifluoromethyl)Group 4A halides reported next, each sample contained unreacted (CFalaHg, the expected (tri-fluoromethyDmercuric halide, and the mercuric halide, identified by fluorine-NMR spectroscopy and mass spectrometry. 

Method development is important. LC-MS performance, probably more than any other technique involving organic mass spectrometry, is dependent upon a range of experimental parameters, the relationship between which is often complex. While it is possible (but not always so) that conditions may be chosen fairly readily to allow the analysis of simple mixtures to be carried out successfully, the widely variable ionization efficiency of compounds with differing structures often makes obtaining optimum performance for the study of all components of a complex mixture difficult. In such cases, the use of experimental design should be seriously considered. 

In a separate set of experiments designed to follow the gas phase reactions of CHj-radicals with NO, CHj- radicals were generated by the thermal decomposition of azomethane, CHjN NCHj, at 980 °C. The CH3- radicals were subsequently allowed to react with themselves and with NO in a Knudsen cell that has been described previously [12]. Analysis of intermediates and products was again done by mass spectrometry, using the VIEMS. Calibration of the mass spectrometer with respect to CH,- radicals was carried out by introducing the products of azomethane decomposition directly into the high vacuum region of the instrument. 

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