Search results for "Trace Amounts"
showing 6 items of 16 documents
Determination of trace amounts of β tegafur in commercial α tegafur by powder X-ray diffractometric analysis.
2011
Abstract Objectives The main objective of this work was to develop a suitable analytical technique for determining trace amounts of the thermodynamically stable solid form in bulk samples of metastable form, to a sensitivity of 0.005%–1.0%. Tegafur (5-fluoro-1-(tetrahydro-2-furyl)-uracil) α and β crystalline forms were used as a model for this problem. Methods The trace content of the thermodynamically stable β polymorphic form in tegafur samples was increased by promoting phase transition from the bulk of thermodynamically metastable α form to β form, and achieving sufficient β form content for a quantitative powder X-ray diffractometry (PXRD) analysis. The phase transition was stimulated …
A selective microscale x-ray fluorescence analyzing method for determination of trace elements
1973
Abstract A new selective X-ray fluorescence analyzing method for trace element determination has been developed. In this method each trace element is measured independently. The excitation source is an X-ray tube that has a changeable anode and a variable high voltage. The exciting radiation is shaped with critical absorbers. The sample is viewed at backward angles through an absorber to reduce backscattered radiation. The estimated accuracy of this method is of the order of 10 per cent in thesub-ppm range of trace element concentration in organic samples. Measurement times are of the order of a few minutes.
Incorporation of trace metals Cu, Zn, and Cd into gypsum: Implication on their mobility and fate in natural and anthropogenic environments
2020
Abstract The coexistence of calcium (Ca2+), sulfate (SO42−) with trace metal cations (M(II)) can possibly lead to M(II)-gypsum coprecipitation and solid solution formation. However, gypsum's role in the fixation of M(II) is still largely unknown. This study investigated the precipitation of Ca2+ and SO42− in the presence of M(II) (i.e., Cu2+, Zn2+, or Cd2+) and the incorporation of the metal cations into the gypsum structure at different environmental conditions. Trace metals in two natural gypsum samples (Yunnan and Neimeng, China) and one hydrometallurgical byproduct gypsum sample from a Cu refinery were also assessed. X-ray diffraction, scanning electron microscopy-energy dispersive X-ra…
Development of accurate mass spectrometric routine and reference methods for the determination of trace amounts of iridium and rhodium in photographi…
1999
For the determination of trace amounts of iridium and rhodium in photographic emulsions different sample treatment procedures were coupled with inductively coupled plasma mass spectrometry (ICP-MS) and, for iridium, also with negative thermal ionisation isotope dilution mass spectrometry (NTI-IDMS) and ICP-IDMS. IDMS determinations of iridium were carried out using an enriched 191Ir spike solution. Elimination of the silver matrix was established for both mass spectrometric methods, which prevents corresponding memory effects in the ICP-MS system and is essential for the formation of IrO2 - thermal ions, respectively. For NTI-MS measurements, the gelatine matrix of the emulsion must also be…
Microfluidic Pumping by Micromolar Salt Concentrations
2017
An ion-exchange-resin-based microfluidic pump is introduced that utilizes trace amounts of ions to generate fluid flows. We show experimentally that our pump operates in almost deionized water for periods exceeding 24h and induces fluid flows of um/s over hundreds of um. This flow displays a far-field, power-law decay which is characteristic of two-dimensional (2D) flow when the system is strongly confined and of three-dimensional (3D) flow when it is not. Using theory and numerical calculations we demonstrate that our observations are consistent with electroosmotic pumping driven by umol/L ion concentrations in the sample cell that serve as 'fuel' to the pump. Our study thus reveals that t…
ANALYTICAL PROCEDURES FOR THE DETERMINATION OF TRACE AMOUNTS OF XENOBIOTICS IN ENVIRONMENTAL WATER SAMPLES
2016
Wciąż wzrastające zanieczyszczenie środowiska związane z działalnością człowieka stanowi poważny problem ekologiczny współczesnego świata. Ksenobiotyki to substancje obce i potencjalnie szkodliwe dla organizmów żywych. Obecność niektórych z nich w środowisku wodnym może nieść za sobą poważne konsekwencje. Do najbardziej niebezpiecznych należą antybiotyki oraz pestycydy. Rozwój nauki i techniki umożliwił kontrolowanie tych substancji w środowisku naturalnym. Oznaczanie śladowych ilości ksenobiotyków w próbkach wód środowiskowych jest złożonym procesem, wymagającym zastosowania odpowiedniej metody ekstrakcyjnej i analitycznej. Złożoność matrycy oraz obecność substancji współobecnych stanowi d…