Efficient Photochemical Vapor Generation from Low Concentration Formic Acid Media.

Herein, we report on surprisingly efficient photochemical vapor generation (PVG) of Ru, Re, and especially Ir, achieved from very dilute HCOOH media employing a thin-film flow-through photoreactor operated in flow injection mode. In the absence of added metal ion sensitizers, efficiencies near 20% for Ir and approximately 0.06% for Ru and Re occur in a narrow range of HCOOH concentrations (around 0.

Highly Efficient Photochemical Vapor Generation for Sensitive Determination of Iridium by Inductively Coupled Plasma Mass Spectrometry.

Herein, we describe the highly efficient photochemical vapor generation (PVG) of a volatile species of Ir (presumably iridium tetracarbonyl hydride) for subsequent detection by inductively coupled plasma mass spectrometry (ICPMS). A thin-film flow-through photoreactor, operated in flow injection mode, provided high efficiency following optimization of identified key PVG parameters, notably, irradiation time, pH of the reaction medium, and the presence of metal sensitizers. For routine use and analytical application, PVG conditions comprising 4 M formic acid as the reaction medium, the presence of 10 mg L Co and 25 mg L Cd as added sensitizers, and an irradiation time of 29 s were chosen.

Non-chromatographic Speciation Analysis of Tellurium by HG-ICP-MS/MS at Sub ng L Concentration in Natural Waters Using Ti as a Pre-Reducing Agent.

An automated and high-throughput (36 h) method for extremely sensitive determination of the two main tellurium species in the environment, namely, tellurite (Te) and tellurate (Te), was developed. Flow injection hydride generation was interfaced for the first time with inductively coupled plasma triple quadrupole mass spectrometry (ICP-MS/MS) detection to assure interference-free tellurium analysis. ICP-MS/MS conditions were studied in detail.

Arsenic species and their health risks in edible seaweeds collected along the Chinese coastline.

Edible seaweeds with a relatively high total arsenic concentration have been a global concern. As the largest seaweed producer, China contributes about 60 % of the global seaweed production. The present study investigated 20 seaweed species collected from representative seaweed farming sites in the six provinces along the Chinese coastline, of which Saccharina japonica, Undaria pinnatifida, Neopyropia spp.

Ultra-sensitive speciation analysis of tellurium by manganese and iron assisted photochemical vapor generation coupled to ICP-MS/MS.

Photochemical vapor generation (PVG) of Te was undertaken with a simple reactor consisting of a polytetrafluoroethylene reaction coil wrapped around a low-pressure mercury tube lamp and using a flow-injection for sample delivery. The composition of a reaction medium, the influence of irradiation time and the effect of added sensitizers and interferents were investigated using high-resolution continuum source atomic absorption spectrometry and a miniature diffusion flame atomizer. A mixture of 5 M acetic acid and 3.

Ultrasensitive Detection of Ruthenium by Coupling Cobalt and Cadmium Ion-Assisted Photochemical Vapor Generation to Inductively Coupled Plasma Mass Spectrometry.

An extremely sensitive methodology for the determination of Ru was developed by coupling photochemical vapor generation (PVG) analyte introduction with inductively coupled plasma mass spectrometry (ICPMS). PVG was undertaken with a thin-film flow-through photoreactor in a medium comprising 8 M formic acid in the presence of 10 mg L Co and 25 mg L Cd. The volatile product (presumably ruthenium pentacarbonyl) was generated in a flow injection mode, yielding an overall efficiency of 29% at a sample flow rate of 1.

A mass spectrometric study of hydride generated arsenic species identified by direct analysis in real time (DART) following cryotrapping.

Hydride generation (HG) coupled to cryotrapping was employed to introduce, separately and with high selectivity, four gaseous arsanes into a direct analysis in real time source for high-resolution mass spectrometry (DART-HR-MS). The arsanes, i.e.

Natural or intended mummification? Specific case of a child mummy.

The aim of this work was to document and analyze an exceptionally preserved mummified body of a six-year-old boy found in a family tomb in Skalná, Czech Republic. The boy died of scarlet fever in 1887, and was buried under ground in a cemetery in an unknown coffin shortly after death. His parents exhumed his cadaver and entombed it in the family crypt in two tin coffins a year later.

Longitudinally monitored lifetime changes in blood heavy metal concentrations and their health effects in urban birds.

Urban heavy metal pollution can impair the health of humans and other organisms inhabiting cities. While birds are suggested as one of the appropriate bioindicators for essential and non-essential trace element monitoring, the process of particular elements' accumulation in blood and its possible adverse health effects during ageing of individuals remain unexplored. We have investigated lifetime changes in blood lead (Pb), cadmium (Cd), arsenic (As) and zinc (Zn) concentrations and searched for links to health-related traits in sub-urban free-living great tit (Parus major) population monitored over a long period of time.

Cadmium Assisted Photochemical Vapor Generation of Tungsten for Detection by Inductively Coupled Plasma Mass Spectrometry.

Efficient photochemical vapor generation (PVG) of tungsten has been achieved for the first time using a 19 W thin film flow-through photoreactor. The volatile product (most probably tungsten hexacarbonyl) was generated using a flow injection mode and 40% (v/v) formic acid as the reaction medium. An inductively coupled plasma mass spectrometer was utilized for ultrasensitive detection.

Na/K-ATPase level and products of lipid peroxidation in live cells treated with therapeutic lithium for different periods in time (1, 7, and 28 days); studies of Jurkat and HEK293 cells.

Regulation of Na/K-ATPase in bipolar disorder and lithium therapy has been investigated for more than 40 years. Contradictory results in this area may be caused by the difference between acute and long-term Li effects on cell metabolism and variance in responsiveness of different cell types. We compared the time-course of Li action focusing on Na/K-ATPase and lipid peroxidation in two widely different cell models-Jurkat and HEK293.

Validation and inter-laboratory study of selective hydride generation for fast screening of inorganic arsenic in seafood.

It is advisable to monitor and regulate inorganic arsenic (iAs) in food and feedstuff. This work describes an update and validation of a method of selective hydride generation (HG) with inductively coupled plasma mass spectrometry (ICP-MS) for high-throughput screening of iAs content in seafood samples after microwave-assisted extraction with diluted nitric acid and hydrogen peroxide. High concentration of HCl (8 M) for HG along with hydrogen peroxide in samples of a same concentration as used for extraction leads to a selective conversion of iAs to volatile arsine that is released and transported to the detector.

Efficient Photochemical Vapor Generation of Molybdenum for ICPMS Detection.

Photochemical vapor generation (PVG) of Mo was accomplished using a 19 W high-efficiency flow-through photoreactor operating in a flow injection mode using 30-50% (w/v) formic acid as a reaction medium. The generated volatile product (most probably molybdenum hexacarbonyl) was directed by an argon carrier gas to a plastic gas-liquid separator and introduced into the spray chamber of an inductively coupled plasma mass spectrometer for detection. Particular attention was paid to the determination of overall PVG efficiency relative to that for liquid nebulization.

Behavior of selenium hydride in heated quartz tube and dielectric barrier discharge atomizers.

Atomization of SeH in an externally heated multiple microflame quartz tube atomizer (MMQTA) as well as planar dielectric barrier discharge (DBD) atomizer was investigated using a variety of probes. Deposits of Se on inner surfaces of the atomizers were quantified and their distribution visualized by autoradiography with Se radiotracer. The gas phase fraction of Se transported beyond the confines of the atomizers was also determined.

Diethyldithiocarbamate enhanced chemical generation of volatile palladium species, their characterization by AAS, ICP-MS, TEM and DART-MS and proposed mechanism of action.

Comprehensive investigation of chemical generation of volatile species (VSG) of palladium for detection by analytical atomic and mass spectrometry and, specifically, the mechanistic aspects of their formation and tentative identification are presented. VSG was achieved in a flow injection mode using a generator that permitted rapid mixing of acidified sample with NaBH reductant. Atomization in a diffusion flame with detection by atomic absorption spectrometry was exclusively used for optimization of generation conditions while inductively coupled plasma mass spectrometry was utilized to investigate overall system efficiency and analytical metrics of the VSG system for potential ultratrace analysis.

Sample preparation for arsenic speciation analysis in baby food by generation of substituted arsines with atomic absorption spectrometry detection.

A slurry sampling procedure for arsenic speciation analysis in baby food by arsane generation, cryogenic trapping and detection with atomic absorption spectrometry is presented. Several procedures were tested for slurry preparation, including different reagents (HNO, HCl and tetramethylammonium hydroxide - TMAH) and their concentrations, water bath heating and ultrasound-assisted agitation. The best results for inorganic arsenic (iAs) and dimethylarsinate (DMA) were reached when using 3molL HCl under heating and ultrasound-assisted agitation.

Direct Speciation Analysis of Arsenic in Whole Blood and Blood Plasma at Low Exposure Levels by Hydride Generation-Cryotrapping-Inductively Coupled Plasma Mass Spectrometry.

A method for analysis of toxicologically important arsenic species in blood plasma and whole blood by selective hydride generation with cryotrapping (HG-CT) coupled either to atomic absorption spectrometry (AAS) with a quartz multiatomizer or to inductively coupled plasma mass spectrometry (ICPMS) has been validated. Sample preparation, which involved only 5 times dilution with addition of Triton X-100, Antifoam B, and l-cysteine, suppressed excessive foaming in a hydride generator. Calibration slopes for whole blood and blood plasma spiked with arsenate, monomethylarsonate, and dimethylarsinate at 0.

Chemical generation of volatile species of copper - Optimization, efficiency and investigation of volatile species nature.

This work is a comprehensive study on chemical generation of volatile species (VSG) of copper for analytical atomic spectrometry. VSG was carried out in a flow injection mode in a special arrangement of the generator. Atomization in a diffusion flame atomizer (DF) with atomic absorption spectrometry detection was mostly used for VSG optimization.

Demethylation of Methylated Arsenic Species during Generation of Arsanes with Tetrahydridoborate(1-) in Acidic Media.

Demethylation during generation of volatile hydrides (HG), i.e. formation of noncorresponding arsanes from monomethylarsonic acid (MAs(V)), dimethylarsinic acid (DMAs(V)), and trimethylarsine oxide (TMAs(V)O) by the reaction of sodium tetrahydridoborate(1-) (THB) with different acids under analytical conditions, was investigated and characterized.

Achieving 100% Efficient Postcolumn Hydride Generation for As Speciation Analysis by Atomic Fluorescence Spectrometry.

An experimental setup consisting of a flow injection hydride generator coupled to an atomic fluorescence spectrometer was optimized in order to generate arsanes from tri- and pentavalent inorganic arsenic species (iAs(III), iAs(V)), monomethylarsonic acid (MAs(V)), and dimethylarsinic acid (DMAs(V)) with 100% efficiency with the use of only HCl and NaBH4 as the reagents. The optimal concentration of HCl was 2 mol L(-1); the optimal concentration of NaBH4 was 2.5% (m/v), and the volume of the reaction coil was 8.