Search results for "Selenium"
showing 10 items of 178 documents
A Method to Quantitatively Trap Volatilized Organoselenides for Stable Selenium Isotope Analysis
2011
If volatile organoselenides are to be analyzed for their stable Se isotope composition to elucidate sources and formation processes, organoselenides need to be trapped quantitatively to avoid artificial Se isotope fractionation. We developed an efficient trap of organoselenides to be used in microcosms designed to determine the Se isotope fractionation by microbial transformation of inorganic Se to volatile organoselenides. The recoveries of volatilized dimethyldiselenide (DMDSe) from aqueous standard solutions by activated charcoal and alkaline peroxide solution with subsequent freeze-drying and purification via a cation exchange resin were tested. Microcosm experiments with the Se-methyla…
Sensing Chiral Drugs by Using CdSe/ZnS Nanoparticles Capped withN-Acetyl-L-Cysteine Methyl Ester
2013
Chiral quantum dots (QDs), differing in their core or shell size and, consequently, in their optical properties, were synthesized by the treatment of commercially available amine-capped quantum dots with methyl ester N-acetyl-L-cysteine (CysP). Interestingly, their colloidal methanol solutions remain stable for several months. Their NMR and IR spectra were in accordance with CysP binding to the QD surface through two anchoring groups; its thiolate (strongly bound) and the carbonyl group of its ester (weaker bound) group, whereas their circular dichroism (CD) spectra showed a new broad redshifted band, suggesting that the attachment to the QD surface modified the conformational equilibrium t…
Synthetic Pathways for New Tubular Transition Metal Hydroxo- and Fluoro-Selenites: Crystal Structures ofM12(X)2(SeO3)8(OH)6(M=Co2+,Ni2+;X= OH−)
1996
The dumortierite-family structuresM12X2(SeO3)8(OH)6(M= Co2+and Ni2+;X= OH−and F−) have been synthesized. The crystal structures of the hydroxo-derivatives have been refined from X?ray powder diffraction data in the space groupP63mc(Z= 1) witha= 12.887(3) A andc= 4.981(4) A (M= Co2+,X= OH−or F−) anda= 12.704(5) A andc= 4.925(6) A (M= Ni2+,X= OH−or F−). Application of the Partial Charge Transference Model allows the understanding of the selenite derivatives crystal chemistry.
Plastic deformation of selenium single crystals ina glide and X-ray observation of the induced substructure
1976
In the plastic deformation of trigonal selenium, a glide in the prismatic planes {1010} is found to be thermally activated, as in tellurium. The activation parameters are determined and a value for the maximum activation energy ΔGmax ≈ (0.6 ± 0.1) eV is obtained. The elastic limit increases up to σ ≈ 100 N mm−2 at low temperatures while it is only σ ≈ 1 N mm−2 at room temperature, i.e. in the athermal region. The deformation induced dislocation substructure is studied by X-ray reflection topography at different temperatures from 77 to 300 K in melt-grown single crystals. It is found that glide polygonization occurs forming rough tilt subgrain boundaries in the prismatic planes. In the ather…
CCDC 156129: Experimental Crystal Structure Determination
2001
Related Article: T.Maaninen, T.Chivers, R.Laitinen, G.Schatte, M.Nissinen|2000|Inorg.Chem.|39|5341|doi:10.1021/ic000598b
Hydride generation atomic fluorescence spectrometric determination of ultratraces of selenium and tellurium in cow milk
2003
Abstract A sensitive procedure has been developed for selenium and tellurium determination in milk by hydride generation atomic fluorescence spectrometry (HG-AFS) after microwave-assisted sample digestion. The method provides sensitivity values of 1591 and 997 fluorescence units ng−1 ml−1 with detection limits of 0.005 and 0.015 ng ml−1 for Se and Te, respectively. The application of the developed methodology to the analysis of cow milk samples of the Spanish market evidenced the presence of concentration ranges from 11.1 to 26.0 ng ml−1 for Se, and from 1.04 to 9.7 ng ml−1 for Te having found a good comparability with data obtained after dry-ashing of samples.
Speciation of selenium and tellurium in milk by hydride generation atomic fluorescence spectrometry
2004
A simple, fast and highly sensitive method has been developed for the differentiation of Se and Te into their (IV) and (VI) oxidation states in milk samples by HG-AFS. This procedure involves a previous leaching of milk slurries by sonication with aqua regia for 10 min. Se(IV) and Te(IV) were determined by analysis of the samples without a pre-reduction step; being total Se and Te determined after reduction with KBr. The method provides limit of detection values (LOD) of 0.012 and 0.023 ng ml−1 for Se(IV) and Te(IV) respectively. Average relative standard deviation values of 10.5%, 3.9%, 12% and 12.5% were found for the determination of Se(IV), Se(VI), Te(IV) and Te(VI) in milk samples cont…
GFAAS determination of selenium in infant formulas using a microwave digestion method.
1994
A method for determining the selenium content of infant formulas is proposed. It includes wet digestion with nitric acid and hydrogen peroxide in medium pressure teflon bombs in a microwave oven and determination by graphite furnace atomic absorption spectrometry (GFAAS). The absence of interferences is checked. Values obtained for the limit of detection (19.4 ng/g), precision (RSD = 2.2%) and accuracy by analysis of a reference material show that the method is reliable.
Multi-pumping mechanised determination of selenium in natural waters by light emitting diode (LED) spectrometry
2009
It has been developed a fully mechanised procedure for the determination of selenium in waters employing a LED based spectrometer and solenoid multi-pumps as solution propelling devices. The proposed method is based on the reaction of selenium with potassium iodide in an acidic medium to liberate iodine, which oxidizes Variamine Blue to form a violet-colour species which absorb at 530 nm. The system was mechanised using the multicommutation process and a stopped flow strategy in the final step reaction. The analytical curve was linear between 0.010 and 0.500 mg L-1, with an equation ΔA = 0.501 (± 0.004) C and r = 0.999. The limit of detection (3σ/S) obtained for the proposed method was 0.00…
Desulfurization: Critical step towards enhanced selenium removal from industrial effluents
2017
Abstract Selenium (Se) removal from synthetic solutions and from real Flue Gas Desulfurization (FGD) wastewater generated by a coal-fired power plant was studied for the first time using a commercial iron oxide impregnated strong base anion exchange resin, Purolite ® FerrIX A33E. In synthetic solutions, the resin showed high affinity for selenate and selenite, while sulfate exhibited a strong competition for both oxyanions. The FGD wastewater investigated is a complex system that contains Se (∼1200 μg L −1 ), SO 4 2− (∼1.1 g L −1 ), Cl − (∼9.5 g L −1 ), and Ca 2+ (∼5 g L −1 ), alongside a broad spectrum of toxic trace metals including Cd, Cr, Hg, Ni, and Zn. The resin performed poorly again…