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Optical Emission Spectrometry (optical + emission_spectrometry)
Kinds of Optical Emission Spectrometry Selected AbstractsSourcing Iron Age softstone artefacts in southeastern Arabia: results from a programme of analysis using Inductively Coupled Plasma-Mass Spectrometry/Optical Emission Spectrometry (ICP-MS/OES)ARABIAN ARCHAEOLOGY AND EPIGRAPHY, Issue 2 2005Peter Magee Iron Age softstone vessels manufactured in southeastern Arabia are widely distributed across that region and in lesser amounts throughout Western Asia. Results from a pilot programme of analysis using Inductively Coupled Plasma Mass Spectrometry/Optical Emission Spectrometry on vessel fragments from two southeast Arabian sites are presented. These results indicate the existence of geochemically distinct groups that are separated by both transition metals and rare earth elements. While this indicates the potential for the application of the provenance postulate in softstone analysis, these promising results need to be further tested by an expanded programme of analysis which includes quarry fragments. [source] Growth and photorefractive properties of Mg:Ce:Cu:LiNbO3 crystals grown by Czochralski methodCRYSTAL RESEARCH AND TECHNOLOGY, Issue 8 2006Y. X. Fan Abstract In this paper, photorefractive properties of Mg:Ce:Cu:LiNbO3 crystals were studied. The crystals doped with different concentration of Mg ions have been grown by the Czochralski method. Mg concentrations in grown crystals were analyzed by an inductively coupled plasma optical emission spectrometry (ICP-OE/MS). The crystal structures were analyzed by the X-ray powder diffraction (XRD), ultraviolet-visible (UV-Vis) absorption spectra and infrared (IR) transmitatance spectra. The photorefractive properties of crystals were experimentally studied by using two-beam coupling. In this experiment we determined the writing time, maximum diffraction efficiency and the erasure time of crystals samples with He-Ne laser. The results showed that the dynamic range (M/#), sensitivity (S) and diffraction efficiency (,) were dependent on the Mg doping concentration, and the Mg(4.58mol%):Ce:Cu:LiNbO3 crystal was the most proper holographic recording media material among the six crystals studied in the paper. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Corrosion of Dental Magnet Attachments for Removable Prostheses on Teeth and ImplantsJOURNAL OF PROSTHODONTICS, Issue 4 2009Arne F. Boeckler DMD, Dr Med Dent Abstract Purpose: For a long time, the use of magnets for the anchorage of dental prostheses failed due to lack of biocompatibility and the magnets' high susceptibility to corrosion in the mouth. These facts make encapsulation of the magnetic alloy with a corrosion-resistant, tight, and functionally firm sealing necessary. Due to different products and analysis methods, it is not feasible to compare the findings for contemporary products with the sparse and rather old test results in the literature. Therefore, the aim of this study was the standardized control and the comparison of the corrosion behavior of modern magnetic attachments for use on teeth and dental implants. Materials and Methods: Thirty-seven components of magnetic attachments on implants and natural teeth from different alloys (NdFeB, SmCo, Ti, CrMoMnTiFe, etc.) as delivered by the manufacturers or fabricated according to their instructions were examined for their corrosion behavior using the statical immersion analysis (ISO 10271:2001). Four specimens of every product with the same design were used. An uncased SmCo magnet served as control. Analyses after 1, 4, 7, and 28 days of the storage in corrosion solution were made. The eluate was examined quantitatively on the alloy components of the respective component with the help of optical emission spectrometry (,g/cm2). The results were compared to the requirements of ISO standard 22674:2006. In addition, existing corrosion products were also defined in the solution after 28 days. The results were analyzed descriptively and statistically to determine possible significant differences (t -test and Mann-Whitney-Wilcoxon rank-sums test; p < 0.05). Results: Dissolved metal ions could be found on all tested products. The release after 1 and 4 days was different for all specimens. In the group of implant abutments, the highest ion release after 7 days was found (all measurements ,g/cm2): Fe (13.94, Magfit-IP-IDN dome type), Pd (1.53, Medical-anchor), Cr (1.32, Magfit-IP-IDN dome type), Ti (1.09, Magfit-IP-IDN abutment), Co (0.81, Medical-anchor), and B (0.6, Magfit-IP-IDN dome type). After 28 days, the analyzed ion release increased irregularly: Fe (173.58, Magfit-IP-IDN dome type), Pd (44.17, Medical-anchor), Cr (2.02, Magfit-IP-IDN dome type), Ti (2.11, Magfit-IP-IDN abutment), Co (26.13, Medical-anchor), B (1.77, Magfit-IP-IDN dome type), and Nd (79.18, Magfit-IP-IDN dome type). In the group of magnetic systems on natural teeth, the highest ion release after 7 days was found for Fe (4.81, Magfit DX 800 keeper), Cr (1.18, Magfit DX 800 keeper), Pd (0.21, Direct System Keeper), Ni (0.18, WR-Magnet S3 small), Co (0.12, Direct System Keeper), and Ti (0.09, Magna Cap , Mini). After 28 days, the analyzed ion release increased non-uniformly: Fe (31.92, Magfit DX 800 Keeper), Cr (6.65, Magfit DX 800 Keeper), Pd (18.19, Direct System Keeper), Ni (0.61, WR-Magnet S3 small), Co (10.94, Direct System Keeper), Ti (0.83, Magna Cap , Mini), and Pd (2.78, EFM Alloy). In contrast, the uncased control magnet showed an exponential release after 7 days of Sm ions (55.06) and Co-ions (86.83), after 28 days of Sm ions (603.91) and Co ions (950.56). The release of corrosion products of all tested products stayed significantly under the limit of 200 ,g/cm2 (ISO 22674:2006). In contrast, the non-encapsulated control magnet exceeded that limit significantly. Conclusion: The analysis of the corrosion behavior of modern magnetic attachments for use on teeth and dental implants according to ISO 10271:2001 showed that metal ions had dissolved on all specimens. In the case of one product, the magnet corroded. For this product, an improvement of the capsulation would be desirable. None of the products reached the limit specified in ISO 22674:2006. All products seem to be suitable for dental application. Further studies in regard to the specific biocompatibility and possible cytotoxic effects on mucosa and tissue would be desirable. [source] Characterisation of avocado (Persea americana Mill) honeys by their physicochemical characteristicsJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 13 2004Anass Terrab Abstract The quality of 12 avocado (Persea americana Mill) honeys from Spain was evaluated. Eight common physicochemical parameters were analysed, namely water content, pH, acidity (free, lactonic and total), sugar content, ash content and electrical conductivity. In addition, the honey samples were analysed using inductively coupled plasma optical emission spectrometry (ICP-OES), and six minerals were quantified for each honey, namely potassium (K), calcium (Ca), magnesium (Mg), sodium (Na), phosphorus (P) and sulphur (S). Most samples showed proper maturity considering the medium water content (mean 17.7%). The total acidity (below 50 meq kg,1 except for one sample) indicated absence of undesirable fermentation; also, the mean pH of around 4.77 is usual in this kind of honey. The values for ash content and electrical conductivity were high (0.77% and 798 µS cm,1 respectively) and typical of dark honeys. K was the predominant mineral (accounting for 73% of the total minerals quantified), followed by Na (10%). Copyright © 2004 Society of Chemical Industry [source] Rf glow discharge optical emission spectrometry for the analysis of arrays of Ni nanowires in nanoporous alumina and titania membranesPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 6 2006V. M. Prida Abstract Anodic alumina (Al2O3) and titania (TiO2) nanoporous oxide membranes are among the most widely studied self-organized nanopore templates, formed by uniform and well aligned arrays of synthetized nanometric pores or tubes. Here, we perform a comparative study of the depth profiling analysis in self-ordered alumina and titania nanoporous membrane templates by means of the radiofrequency glow discharge coupled to optical emission spectrometry (rf-GD-OES) technique. The densely packed columnar arrays of hexagonally self-ordered nanoporous alumina membranes investigated, with an average inner pore diameter of 35 nm and 105 nm interspacing, give an uniform thickness pore length about more than 5 µm, depending on the anodization time. Meanwhile, the analysis of the anodized titania nanotubes, with an average inner pore diameter of 100 nm and 40 nm wall thickness, shown to be about 300 nm in length. Each type of membranes were also studied in both cases, when the nanopores were empty and after filling with electrodeposited Ni. The direct analysis by rf-GD-OES reveals the ability of this technique to control the quality of these so synthesized nanocomposites formed by electrodeposited Ni nanowires into the alumina and titania nanoporous templates. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Determination of refractory elements in atmospheric particulates using slurry sampling electrothermal vaporization inductively coupled plasma optical emission spectrometry and inductively coupled plasma mass spectrometry with polyvinylidene fluoride as chemical modifierRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 14 2006Yuefei Zhang Electrothermal vaporization (ETV) inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS) with polyvinylidene fluoride (PVDF) as chemical modifier are critically compared for the determination of refractory elements in coal fly ash and airborne particulates. The atmospheric particulates that collected on a PVDF filter were introduced into the graphite furnace in the form of a slurry by dissolving the filter in dimethylformamide, and the dissolved filter PVDF, along with additional added PVDF powder, was used as a chemical modifier for subsequent ETV-ICP-OES and ETV-ICP-MS determination. The vaporization behaviors of analytes (Ti, Zr, V, Mo, Cr, La) in ETV-ICP-OES/MS were studied in detail, and the optimal ETV operating parameters were obtained. Under the optimized operating conditions, the detection limits of target elements were 0.08,2.7,ng,m,3 for ETV-ICP-OES and 0.5,50,pg,m,3 for ETV-ICP-MS, respectively, with analytical precisions of 3.5,7.3% for ETV-ICP-OES and 3.9,9.6% for ETV-ICP-MS, respectively. The tolerable amounts of matrix elements for ETV-ICP-OES are higher than for ETV-ICP-MS. Both ETV-ICP-OES and ETV-ICP-MS were used to directly determine the trace refractory elements in coal fly ash and airborne particulates and the analytical results are comparable. Copyright © 2006 John Wiley & Sons, Ltd. [source] | |||||||||||||