Sample preparation surface chemical state

This technique can be applied to samples prepared for study by scanning electron microscopy (SEM). When subject to impact by electrons, atoms emit characteristic X-ray line spectra, which are almost completely independent of the physical or chemical state of the specimen (Reed, 1973). To analyse samples, they are prepared as required for SEM, that is they are mounted on an appropriate holder, sputter coated to provide an electrically conductive surface, generally using gold, and then examined under high vacuum. The electron beam is focussed to impinge upon a selected spot on the surface of the specimen and the resulting X-ray spectrum is analysed. 

Sampling and Measurements. The determination of dissolved actinide concentration was started a week after the preparation of solutions and continued periodically for several months until the solubility equilibrium in each solution was attained. Some solutions, in which the solubilities of americium or plutonium were relatively high, were spectrophotometrically analyzed to ascertain the chemical state of dissolved species. For each sample, 0.2 to 1.0 mL of solution was filtered with a Millex-22 syringe filter (0.22 pm pore size) and the actinide concentration determined in a liquid scintillation counter. After filtration with a Millex-22, randomly chosen sample solutions were further filtered with various ultrafilters of different pore sizes in order to determine if different types of filtration would affect the measured concentration. The chemical stability of dissolved species was examined with respect to sorption on surfaces of experimental vials and of filters. The experiment was performed as follows the solution filtered by a Millex-22 was put into a polyethylene vial, stored one day, filtered with a new filter of the same pore size and put into another polyethylene vial. This procedure was repeated twice with two new polyethylene vials and the activities of filtrates were compared. The ultrafiltration was carried out by centrifugation with an appropriate filter holder. The results show that the dissolved species in solution after filtration with Millex-22 (0.22 ym) do not sorb on surfaces of experimental materials and that the actinide concentration is not appreciably changed with decreasing pore size of ultrafilters. The pore size of a filter is estimated from its given Dalton number on the basis of a hardsphere model used in the previous work (20). 

In recent decades we have seen an explosion of various spectroscopic techniques for analyzing the elemental composition and chemical states of solid surfaces and films. This explosion has stemmed in part from the large number of surface- or interface-related problems seen in integrated-circuit performance, composite reliability, corrosion, nanostructured components, and so on. Instruments themselves can range from stand-alone units to attachments in national synchrotron facilities or multitechnique systems built around special fabrication sites. However, the basic principle of the technique, and therefore the basic concerns with sample preparation, stay the same. 

After chemical analysis with XPS at the various states of samples preparation, imaging ToF-SIMS analysis was applied to identify characteristic fragments of MAD-Gal at the surface. Figure 3 illustrates the negative F ion distribution on a masked-assisted patterned sample after photobonding. 

One of the most significant developments in mass spectrometry in the recent years is the introduction of a new class of ionization methods where samples in either solid or liquid state can be directly ionized in their native environment under ambient conditions (rather than inside a mass spectrometer) without any sample preparation. This new class of ionization methods is often referred to as ambient ionization methods [1,2], Because these methods generally ionize analytes on the surface or near the surface of the samples at atmospheric pressure, they have also been called atmospheric pressure surface sampling/ionization methods or direct/open air ionization methods [3], Since the first reports on ambient ionization with desorption electrospray ionization (DESI) [4] and direct analysis in real time (DART) [5], numerous reports have been published on the applications of these new ionization methods as well as the introduction of many related ambient ionization methods such as desorption atmospheric pressure chemical ionization (DAPCI) [6], atmospheric solid analysis probe (ASAP) [7], and electrospray-assisted laser desorption/ionization (ELDI) [8], Recently, two reviews of the various established and emerging ambient ionization methods have been published [2,3],... 

The technique of optical and ultraviolet reflectance spectroscopy, as described earlier, provides still another physical-chemical technique which can be used to study chromia-alumina catalysts. Like ESR and NMR, it has the advantage of being applicable to powdered, commercial catalysts without the necessity of special sample preparation. In the present section, some typical reflection spectra of chromia-alumina catalysts will be presented, and it will be shown that these spectra provide a measure of the amount of chromium present in the 6-f oxidation state. Reflectance spectroscopy is particularly useful here because the Cr + ion is diamagnetic, and hence cannot be detected by the usual magnetochemical or ESR techniques. In addition, it turns out that the intensity of the reflectance spectrum of a chromia-alumina catalyst is directly related to the extent to which the surface of the catalyst is covered with chromia, and thus the surface composition of such a catalyst can be roughly estimated from its optical spectrum. 

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