The sorption properties of carbon-composite materials based on montmorillonite and hydrotalcite matrices have been studied using nitrogen adsorption isotherms and inverse gas chromatography. Carbon composite materials derived from both types of inorganic precursors contain pore structure accessible for adsorbate molecules. Adsorption capacity per unit mass of these composite adsorbents is larger in the case of hydrotalcite than in montmorillonite-based materials. Exposing these materials to ambient conditions results in their hydration. Subsequent water removal by heating under vacuum increases nitrogen adsorption capacity, which is explained by the opening of the adsorption space. The water content of hydrated samples and its effect on adsorption capacity is greater for the case of hydrotalcite-based materials. No direct relationship between carbon content and adsorption properties of the materials studied is observed.

The lithium form of taeniolite served as the molecular template for carbon nanocomposites. It was intercalated with hydroxy aluminum and hydroxy aluminum-zirconium cations. Aliquots of the inorganic matrices were saturated by furfuryl alcohol followed by its interlayer polymerization. The structures were heated at 973 K in nitrogen to carbonize the polymeric precursor. Additional materials were mixed with polypropylene glycol which was then carbonized within the mineral layers. The surface properties of the nanocomposites were studied by X-ray diffraction (XRD), DTA, SEM and sorption experiments (sorption of nitrogen). The results showed that structural properties of the derived materials depend on the inorganic matrix and organic precursor. The carbon-taeniolite nanocomposites derived from polyfurfuryl alcohol as a precursor were characterized by high carbon content and a high percentage of its surface area in micropores. A broad spectrum of surface characteristics of the final products were found, depending on the history of the sample.

FF-GDMS and MIC-ICP-MS methods were developed for the determination of mg/kg- and μg/kg-level B, Mg, Al, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Zr, Mo, Sb, W and Pb in nuclear-grade graphite. Consistent results have been achieved in determining trace elements like B, Ti, Cr, Mn, Zr, Sb and Pb by both methods, which vary mostly less than ±30%, and are in line with the manufacturer reference values. On Mg, Al, Fe, Co, Zn, Mo and W, FF-GDMS analyses also show good agreement with the manufacturer's data. Continuing efforts in identifying source of interference, which has limited the MIC-ICP-MS analysis of these elements, is currently underway.

The calibration factors are examined for determination of boron (B) and phosphorus (P) in solar grade silicon samples in the new generation of high resolution fast-flow glow-discharge mass spectrometers (FF-GDMS). It is shown that using the generalized calibration factors from the Standard RSF table, the relative errors observed in the determination of these analytes is not acceptably small for photovoltaic applications. The certified B and P values in NIST SRM 57a Si metal sample do not have the confidence intervals, which would be adequate for refining these calibration factors to the acceptable levels. Thus, well-characterized single crystalline Si wafers with known boron and phosphorus contents traceable to NIST reference materials (SRM 2133 and SRM 2137) were used for accurate calibrations and for establishing good analytical procedures for measurements of wide variety of Si sample forms. The obtained results for these important analytes using the new FF-GDMS procedure are compared to other characterization techniques commonly used in this industry.