Inductively Coupled Plasma Mass Spectrometry(ICP-Ms). Inorganic Elements
This analysis is suitable for the following elements; Ag, Al, As, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cr, Cs, Cu, Dy, Er, Eu, Fe, Ga, Gd, Ge, Hf, Hg, Ho, In, Ir, K, La, Li, Lu, Mg, Mn, Mo, Na, Nb, Nd, Ni, Os, P, Pb, Pd, Pr, Pt, Re, Rh, Ru, S, Sb, Sc, Se, Si, Sn, Sr, Ta, Tb, Th, Ti, Tl, Tm, U, V, W, Y, Yb, Zn, and Zr. The elements Hg, Os and S may be analyzed by special arrangement with the laboratory. Cesium can only be measured by ICPMS.
Inductively Coupled Plasma Mass Spectrometry(ICP-Ms)/Semi Quantitiative Scan of Inorganic Elements
This analysis is suitable for the following elements; Ag, Al, As, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cr, Cs, Cu, Dy, Er, Eu, Fe, Ga, Gd, Ge, Hf, Hg, Ho, In, Ir, K, La, Li, Lu, Mg, Mn, Mo, Na, Nb, Nd, Ni, Os, P, Pb, Pd, Pr, Pt, Re, Rh, Ru, S, Sb, Sc, Se, Si, Sn, Sr, Ta, Tb, Th, Ti, Tl, Tm, U, V, W, Y, Yb, Zn, and Zr. The elements Hg, Os and S may be analyzed by special arrangement with the laboratory. Cesium can only be measured by ICPMS.
Flame Atomic Absorption Spectroscopy or emission.(FLAA) Inorganic Elements
This analysis is suitable for the following elements; Al, Ag, Ba, Bi, B, Ca, Cd, Cr, Co, Cu, Ga, K, Fe, Pb, Li, Mg, Mn, Mo, Na, Ni, Pd, Pt, Rh, Ru, Sb, Se, Si, Sn, Ti, V and Zn. Other elements may be analyzed by special arrangement with the laboratory. The technique is best used for alkali metals. Solid samples requiring lower limits of detection must use either GFAA, ICP or ICPMS depending on the element.
Graphite furnace atomic absorption.(GFAA) Inorganic Elements
This analysis is suitable for the following elements; Al, Ag, Ba, Bi, Cd, Cr, Co, Cu, Ga, Fe, Pb, Li, Mn, Mo, Ni, Pd, Pt, Rh, Ru, Se, Si, Sb, Sn, Ti, V and Zn. Other elements may be analyzed by special arrangement with the laboratory. Solid samples requiring lower limits of detection must use either ICP or ICPMS depending on the element.
This analysis is suitable for samples containing residual solvents at levels ranging from trace amounts (typical 0.01% quantitation limit using 100 mg sample size) to a relative high percentage.
This analysis is suitable for samples containing residual solvents at levels ranging from trace amounts (typical 0.01% quantitation limit using 100 mg sample size) to a relative high percentage.
This analysis is suitable for identification of unknown residual solvents at levels ranging from trace amounts (typical 0.05% quantitation limit using 100 mg sample size) to a relative high percentage.
This analysis consists of acquiring the infrared spectrum of a given compound. The spectrum is indicative of the vibrations between atoms in the molecule. Therefore, it can be used to identify the structure of a molecule.
This analysis consists of acquiring the ultraviolet and visible spectrum of a given compound. The spectrum is indicative of electron transitions between the orbitals in the molecule. Therefore, it can be used to identify the structural features of a molecule.
This analysis is suitable for samples containing water at high levels, 0.5% to 10%. Additionally, a large amount of sample is usually required for accurate results. For smaller sample sizes and lower detection limits use Coulometric Karl Fischer titration.
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