Search results for "Trace analysis"
showing 10 items of 26 documents
Investigation of the Electrophoretic Mobility of the Actinides Th, U, Np, Pu, and Am in Different Oxidation States.
2019
The electrophoretic mobilities (μe) of the actinides Th and U-Am in different oxidation states (prepared in 1 M HCl and 1 M HClO4) have been determined by capillary electrophoresis (CE)-inductively coupled plasma mass spectrometry (ICPMS) using 1 M acetic acid as the background electrolyte, which has proven to provide an excellent setup for trace analysis at environmentally relevant concentrations (1 × 10-9 M). The values are independent of the respective acid solution. The μe of the Pu oxidation states +III to +VI have been measured. They agree with both the available literature data and the redox-stable analogues (Eu(III), Th(IV), Np(V), U(VI)) that have also been investigated. The trend …
Determination of trimethoprim by the linear absorbances method
1995
The determination of trimethoprim in the presence of dyphylline, proxyphylline, theophylline and caffeine by the linear absorbances method is described. Collinear couples of wavelengths, for the interfering dyphylline-proxyphylline-theophylline-caffeine system (in H2SO4, 0.05 mol/L), are provided in order to allow the determination of the analyte in the presence of these interfering substances.
Evaluation of Thin Film Microextraction for trace elemental analysis of liquid samples using LIBS detection
2021
An analytical methodology based in the combination of Thin Film Microextraction with Laser-induced Breakdown Spectroscopy (TFME-LIBS) was investigated, for the first time, for detection of Cu, Cr, Ni and Pb in aqueous solutions. In this methodology, the analytes were extracted in a thin film of adsorbent material deposited on a solid support, which was introduced in the sample to analyse. After extraction, the analytes retained in the adsorbent were analysed by LIBS. In order to obtain adsorbent films useful for the microextraction step, two different experimental procedures for film generation, denoted as Drop Casting Deposition and Mould Deposition, were evaluated. In both cases, graphene…
Recent developments in resonance ionization mass spectrometry for ultra-trace analysis of actinide elements
2019
Abstract Resonance ionization mass spectrometry is an efficient tool to detect minute amounts of long-lived radio-isotopes in environmental samples. Applying resonant excitation and ionization with pulsed laser radiation within a hot cavity atomizer enables the sensitive detection and precise quantification of long-lived actinide isotopes. Due to the inherently element selective ionization process, this method ensures ultimate suppression of contaminations from other elements and molecules. The characterization of in-source resonance ionization of the actinide elements U, Th, Np, and Am using a compact quadrupole mass spectrometer (QMS) setup are discussed.
Evaluation by HPLC-UV of Polar Pesticides in Rice Fields
1999
Solid-phase extraction of quaternary ammonium herbicides
2000
This paper highlights recent advances in the solid-phase extraction (SPE) of quaternary ammonium herbicides in water, soil, plant and biological samples. After a brief introduction summarizing the properties of quaternary ammonium herbicides and the difficulties involved in measuring them, attention is paid primarily to solid supports used for isolation and concentration, pre-treatments required for the different matrices, and eluents applied for quantitative desorption of these analytes. The determination techniques used after SPE and applications of the proposed SPE methodology are also briefly discussed.
4 th Symposium on Mass Spectrometric Methods for Element Trace Analysis
1999
Spectrophotometric determination of phenol and resorcinol by reaction with p-aminophenol
1993
Abstract Based on the reaction with p-aminophenol, a series of procedures have been developed for the spectrophotometric determination of phenol and resorcinol. Three basic approaches have been studied: (i) a batch procedure, using the dissolved oxygen as oxidant, (ii) a stopped-flow procedure by use of KIO4 as oxidant and (iii) a flow injection (FI) procedure developed in the presence of KIO4. Phenol can be accurately determined at 626 nm, in the stopped-flow mode, after a reaction time of 45 min in 0.005M NaOH, 0.004M KIO4 and 500 μg/ml of PAP. The development of a manifold, which incorporates a sample parking, is a convenient approach which makes it possible to measure, in the stopped-fl…
Rapid microwave assisted hydrolysis of formetanate
1993
Abstract A fast microwave-assisted hydrolysis procedure has been developed for the derivatization of formetanate previously to the flow-injection spectrophotometric determination of m -aminophenol by reaction with p -aminophenol. Formetanate is quantitatively hydrolyzed with 0.1 M NaOH in 150 s using a closed polyetrafluoroethylene reactor with 115 ml internal volume and a radiation power of 390 W. The above procedure has been applied, as a previous step, for the flow-injection spectrophotometric determination of formetanate in spiked water samples and accurate and precise results have been found. The method permits to obtain a limit of detection of 0.025 mg 1 −1 of formetanate. The relativ…
Resonance ionization mass spectrometry for trace analysis of long-lived radionuclides
2008
Resonance ionization mass spectrometry (RIMS) is a sensitive and selective method for the determination of extremely low abundances of long-lived radionuclides. The detection limits are about 106 atoms per sample and an isotopic selectivity up to 1013 has been achieved. The potential of RIMS using different experimental arrangements is outlined for the determination of isotope ratios and lowest abundances of long-lived radioisotopes of interest like 238–244Pu, 90Sr, and 41Ca. Recent developments in improving detection limits and the spatial resolution of this technique are briefly discussed.