Volatile Selenium Research Articles

Achromobacter seleniivolatilans sp. nov. and Buttiauxella selenatireducens sp. nov., isolated from the rhizosphere of selenium hyperaccumulator Cardamine hupingshanesis.

Two Gram-stain-negative bacterial strains, R39T and R73T, were isolated from the rhizosphere soil of the selenium hyperaccumulator Cardamine hupingshanesis in China. Strain R39T transformed selenite into elemental and volatile selenium, whereas strain R73T transformed both selenate and selenite into elemental selenium. Phylogenetic and phylogenomic analyses indicated that strain R39T belonged to the genus Achromobacter, while strain R73T belonged to the genus Buttiauxella. Strain R39T (genome size, 6.68 Mb; G+C content, 61.6 mol%) showed the closest relationship to Achromobacter marplatensis LMG 26219T and Achromobacter kerstersii LMG 3441T, with average nucleotide identity (ANI) values of 83.6 and 83.4 %, respectively. Strain R73T (genome size, 5.22 Mb; G+C content, 50.3 mol%) was most closely related to Buttiauxella ferragutiae ATCC 51602T with an ANI value of 86.4 %. Furthermore, strain A111 from the GenBank database was found to cluster with strain R73T within the genus Buttiauxella through phylogenomic analyses. The ANI and digital DNA-DNA hybridization values between strains R73T and A111 were 97.5 and 80.0% respectively, indicating that they belong to the same species. Phenotypic characteristics also differentiated strain R39T and strain R73T from their closely related species. Based on the polyphasic analyses, strain R39T and strain R73T represent novel species of the genera Achromobacter and Buttiauxella, respectively, for which the names Achromobacter seleniivolatilans sp. nov. (type strain R39T=GDMCC 1.3843T=JCM 36009T) and Buttiauxella selenatireducens sp. nov. (type strain R73T=GDMCC 1.3636T=JCM 35850T) are proposed.

Effects of sodium selenite on the growth, biochemical composition and selenium biotransformation of the filamentous microalga Tribonema minus

This study aimed to investigate the physiological and biochemical responses of filamentous microalga Tribonema minus to different Na2SeO3 concentrations and its selenium absorption and metabolism to evaluate the potential in treating selenium-containing wastewater. The results showed that low Na2SeO3 concentrations promoted growth by increasing chlorophyll content and antioxidant capacity, whereas high concentrations caused oxidative damage. Although Na2SeO3 exposure reduced lipid accumulation compared with the control, it significantly increased carbohydrate, soluble sugar, and protein contents, with the highest carbohydrate productivity of 117.97 mg/L/d at 0.5 mg/L Na2SeO3. Furthermore, this alga effectively absorbed Na2SeO3 in the growth medium and converted most of it into volatile selenium and a small part into organic selenium (predominantly as selenocysteine), showing strong selenite removal efficacy. This is the first report on the potential of T. minus to produce valuable biomass while removing selenite, providing new insights into the economic feasibility of bioremediation of selenium-containing wastewater.

Draft Genome Sequence of Stutzerimonas stutzeri NT-I, Which Reduces Selenium Oxyanions into Elemental Selenium and Volatile Selenium Species.

Stutzerimonas stutzeri strain NT-I effectively reduces selenate and selenite into elemental selenium and volatile selenium species. It is thus a promising biological agent for treatment of selenium-contaminated wastewater. We here report the draft genome sequence of this strain.

Condensation and adsorption characteristics of gaseous selenium on coal-fired fly ash at low temperatures

Gaseous selenium is of high saturated vapor pressure, making its retention in solid phases quite difficult during coal combustion. The selenium transformation from gaseous form into solid phases at low temperatures can be essential to control selenium emission. To understand the migration of SeO2 (g) on ash particles in the low-temperature zone, this study investigated the speciation of selenium in fly ash and simulated the physical retention of SeO2 (g) on fly ash. The results demonstrated that there was a large proportion of physically-bound Se in the fly ash of pulverized-coal-fired boiler (22.62 %–58.03%), while the content of physically-bound Se in fly ash of circulated fluidized-bed boiler was lower (∼6%). The physically-bound Se was formed through selenium condensation and physical adsorption. The decrease of temperature or the increase of cooling rate could promote the transformation of gaseous selenium to solid phase and the presence of HCl might suppress SeO2 transformation into Se in the condensation process. Meanwhile the compositions of fly ash had a great influence on the selenium adsorption process. Among typical coal-fired ash components, mullite showed the best performance in the selenium capture in the temperature range of 90–200 °C, contributing to the high content of physically-adsorbed selenium in PC fly ash. These findings provided new ideas for improving the removal rate of volatile selenium.

In-vivo solid phase microextraction for quantitative analysis of volatile organoselenium compounds in plants

A new calibration method based on the use of headspace solid-phase microextraction (HS-SPME) and in-fiber internal standardization, combined with gas chromatography coupled to mass spectrometry (GC/MS) was developed for quantifying Se volatile organic species released by plants exposed to chitosan-modified selenium nanoparticles (Cs-SeNPs). The effect of several parameters affecting extraction and separation of the selected organic species of selenium (dimethylselenium (DMSe), diethylselenium (DESe) and dimethyldiselenium (DMDSe)) and deuterated dimethyl sulphide (d6-DMS) employed as internal standard were studied and optimized using an experimental design. The developed methodology was applied for quantifying the volatile selenium compounds produced over time by the plant species Raphanus sativus and Brassica juncea grown in hydroponic solution containing 5 mg Se L−1 in the form Cs-SeNPs. The procedure employed consisted in two steps. Volatile selenium species released from the plants were first extracted in the SPME fiber located at the headspace of a box with a fixed volume. Subsequently, the internal standard placed in a vial subjected to the same conditions as plants was extracted on the same fiber than the one previously used for extracting selenium compounds. Finally the extracted compounds were separated and analyzed by GC/MS. Results evidenced Cs-SeNPs biotransformation into DMSe and DMDSe by both plants species during growing stage, in amounts of the order of ng. Additionally, the resulting data were submitted to multifactorial ANOVA to evaluate the influence of plant type and time of exposure to Cs-SeNPs on the production of volatile selenium compounds.

Combustion characteristics and retention-emission of selenium during co-firing of torrefied biomass and its blends with high ash coal

The combustion characteristics, kinetic analysis and selenium retention-emission behavior during co-combustion of high ash coal (HAC) with pine wood (PW) biomass and torrefied pine wood (TPW) were investigated through a combination of thermogravimetric analysis (TGA) and laboratory-based circulating fluidized bed combustion experiment. Improved ignition behavior and thermal reactivity of HAC were observed through the addition of a suitable proportion of biomass and torrefied. During combustion of blends, higher values of relative enrichment factors in fly ash revealed the maximum content of condensing volatile selenium on fly ash particles, and depleted level in bottom ash. Selenium emission in blends decreased by the increasing ratio of both PW and TPW. Higher reductions in the total Se volatilization were found for HAC/TPW than individual HAC sample, recommending that TPW have the best potential of selenium retention. The interaction amongst selenium and fly ash particles may cause the retention of selenium.

Studying selenium and sulfur volatilisation by marine algae Emiliania huxleyi and Thalassiosira oceanica in culture

Environmental contextVolatile selenium compounds from the oceans may ultimately be an important selenium source for agricultural soils. It has been hypothesised that marine algae are responsible for volatile selenium emissions, but in laboratory experiments, we observed minimal volatile selenium production by two marine algae known to produce large amounts of volatile sulfur. Instead, we found hints that bacterial processes may be important in the production of volatile selenium in the oceans. AbstractVolatile methylated selenium compounds, especially dimethylselenide, are thought to comprise the majority of marine selenium emissions. Despite their potential importance for the global redistribution of this trace element, which is essential for human health, little is known about the algal production of volatile organic selenium compounds. Previous studies have found correlations between dissolved dimethylselenide concentrations, dimethylsulfide concentrations (the sulfur analogue of dimethylselenide) and proxies for algal activity, most notably during a bloom of the coccolithophorid Emiliania huxleyi. In culturing studies, we investigated the ability of three globally important marine algal species, E. huxleyi, Phaeocystis globosa and the diatom Thalassiosira oceanica, to produce dimethylselenide. Despite substantial uptake of selenium and the production of volatile sulfur, E. huxleyi and T. oceanica produced negligible volatile selenium (<2nM). P. globosa produced low amounts of volatile selenium (~8nM), but grew poorly in our laboratory. However, cultures of marine bacteria and mixed bacterial–algal cultures showed that substantial amounts of volatile selenium can be produced in the presence of marine bacteria. In addition, a culture of marine bacteria alone produced ~50nM volatile selenium, far more than axenic cultures of E. huxleyi when exposed to equivalent selenite concentrations. Our results hint that marine algae may be of minor importance in the direct production of volatile selenium in the oceans, and suggest that the production of these compounds in the marine biosphere may instead be controlled by bacterial activity.

Analysis of Means (ANOM) as a Tool for Comparison of Sample Treatment Methods: Testing Various Mineralization Procedures for Selenium Determination in Biological Materials.

Several mineralization methods for the determination of selenium using hydride generation optical emission spectrometry with inductively coupled plasma in biological samples (whole egg powder and pork liver) were compared using the analysis of means (ANOM) method. This statistical tool is suitable for graphical representation of testing on simple comparative experiments. The results yielded by ANOM are identical with those obtained with the commonly used analysis of variance (ANOVA) method; however, the graphical output of ANOM is more illustrative in comparison to ANOVA. Both methods indicated a significant discrepancy between the results obtained using muffle furnace ashing mineralization and the results provided by other mineralization methods. This is probably due to the loss of volatile selenium compounds during the decomposition of organic matter.

Optimization of Electrochemically Deposited Highly Doped ZnO Bilayers on Ga-Rich Chalcopyrite Selenide for Cost-Effective Photovoltaic Device Technology

High quality polycrystalline bilayers of aluminium doped ZnO (Al:ZnO) were successively electrodeposited in the form of columnar structures preferentially oriented along the ( 10 1 ¯ 1 ) crystallographic direction from aqueous solution of zinc nitrate (Zn(NO3)2) at negative electrochemical potential of EC = (−0.8)–(−1.2) V and moderate temperature of 80 °C on gallium rich (30% Ga) chalcopyrite selenide Cu(In,Ga)Se2 (CIGS) with chemically deposited ZnSe buffer (ZnSe/Cu(In,Ga)Se2/Mo/glass). The aluminium doped ZnO layer properties have initially been probed by deposition of Al:ZnO/i-ZnO bilayers directly on Mo/glass substrates. The band-gap energy of the Al:ZnO/i-ZnO reference layers was found to vary from 3.2 to 3.7 eV by varying the AlCl3 solute dopant concentration from 1 to 20 mM. The electrical resistivity of indium-pellet contacted highly doped Al:ZnO sheet of In/Al:ZnO/i-ZnO/Mo/glass reference samples was of the order ρ ~10−5 Ω·cm; the respective carrier concentration of the order 1022 cm−3 is commensurate with that of sputtered Al:ZnO layers. For crystal quality optimization of the bilayers by maintenance of the volatile selenium content of the chalcopyrite, they were subjected to 2-step annealing under successive temperature raise and N2 flux regulation. The hydrostatic compressive strain due to Al3+ incorporation in the ZnO lattice of bilayers processed successively with 5 and 12 mM AlCl3 dopant was εh = −0.046 and the respective stress σh = −20 GPa. The surface reflectivity of maximum 5% over the scanned region of 180–900 nm and the (optical) band gap of Eg = 3.67 eV were indicative of the high optical quality of the electrochemically deposited (ECD) Al:ZnO bilayers.

Studies on photochemical vapor generation of selenium with germicidal low power ultraviolet mercury lamp

Photochemical vapor generation (photo-CVG) with flow injection - atomic fluorescence spectrometry was investigated for the determination of selenium, using formic and acetic acids as photochemical reagents. Using a germicidal low power ultraviolet mercury-based lamp, emitting both the 185 and 254nm Hg lines, mild reaction conditions can be achieved in formic acid medium, where optimal sensitivity was obtained at 0.3–0.5% w/w acid concentrations, whereas the optimal sensitivity could be attained with acetic acid in the range from 12 to 35% w/w. The only volatile Se product identified by gas chromatography–mass spectrometry from formic acid-based photo-CVG was selenium carbonyl. A series of dedicated experiments were performed using photo-CVG and pure dimethylselenide in order to identify reaction pathways contributing to the formation of non-volatile selenium species or to the degradation of volatile selenium species. Under the optimized conditions in formic acid, using 250μL sample volume, the limits of detection and quantification were 0.10 and 0.35μgL−1, respectively. The effect of several interfering species was investigated and the method was tested in the analysis of certified reference materials.

A time-efficient flow injection/ICPMS method for the direct determination of total selenium in human urine

Selenium, an essential trace element with many biochemical functions, shows toxic effects at elevated intake. Therefore, it is important to monitor the selenium body status e.g. by investigating total selenium in biological fluids like urine. Inductively coupled plasma mass spectrometry (ICPMS) is a robust technique with low limits of detection for the determination of total selenium in body fluids. When flow injection (FI) is used to introduce the sample to the ICPMS, low sample volumes can be investigated directly, without time-consuming digestion steps. We describe a time-efficient method for determining total selenium in urine using a simple filtration step for sample preparation and measurement by FI/ICPMS. Quantification was based on external calibration without time-consuming standard addition approaches. Matrix effects occurring when urine is analysed directly without dilution were minimized by splitting the flow of the carrier solution, by optimizing the injection volume, and by using germanium as internal standard. Best results were obtained with 20mM malonate 3% methanol pH6.0 containing 50μgGeL−1 as carrier solution at a flow rate of 1.5mLmin−1, whereby 15% of the carrier solution was directed to the ICPMS by a passive splitter, and an injection volume of 5μL. The method limit of detection (LOD) and quantification (LOQ) in urine were 0.07μgSeL−1 and 0.2μgSeL−1, respectively. The accuracy of the method was evaluated by (i) the certified reference material NIES No. 18 Human urine and (ii) comparison of FI/ICPMS results for different urine samples with target concentrations obtained by ICPMS after microwave-assisted acid digestion. Urine samples could be stored at 4°C for at least 4days, before the formation of volatile selenium compounds led to overestimated results. Intra-day precision for the determination of total selenium in urine was about 3% (n=3) and inter-day precision about 5% (n=3). Simple sample preparation by only filtration, a short analysis time, and the low requirement for sample volume makes the method very useful particularly for large numbers of samples and samples for which only limited volumes are available.

UV-photochemical vapor generation of selenium for atomic absorption spectrometry: Optimization and 75Se radiotracer efficiency study

Volatile selenium compounds were generated UV-photochemically in the continuous flow mode using four UV-photoreactors differing in the material of the reaction coil; Teflon tubing and quartz tubes with various inner diameters and wall thicknesses were tested. Atomic absorption spectrometry with an externally heated quartz furnace atomizer was employed as the detector. The relevant experimental generation parameters were optimized and the basic analytical characteristics were determined. Using formic acid as the photochemical agent, limits of detection achieved for selenium were in the range 46–102ngL−1 in dependence on the type of UV-photoreactor employed. When nitric acid was also added to the photochemical agent, the limits of detection were reduced to 27–44ngL−1. The repeatability did not exceed 2.4% (5μgL−1 Se(IV), n=10). Experiments with 75Se radiotracer have been performed for the first time to quantify the efficiency of UV-photochemical vapor generation (UV-PVG) of selenium. The highest efficiency of 67±1% was obtained for a UV-photoreactor containing a quartz reaction coil (2.0mm i.d., 4.0mm o.d.). The generation efficiency of 61±1% was obtained for a Teflon reaction coil (1.0mm i.d., 1.4mm o.d.). Mapping of the radiotracer distribution in the individual parts of the apparatus did not reveal substantial transport losses of the analyte in the UV-PVG system.

Volatile selenium fluxes from selenium-contaminated sediments in an Australian coastal lake

Environmental context Methylation of sedimentary selenium to volatile dimethylselenide is a natural remediation process for contaminated aquatic systems. We present flux estimates for the loss of dimethylselenide from sediments of an anthropogenically affected lake and observe a 6-fold difference between late autumn–early winter and summer. The loss of dimethylselenide represents a significant sediment loss vector, of the same order as the diffusive loss flux for inorganic selenium across the sediment–water interface. Abstract Overflows from ash dams associated with the operation of coal-fired power stations in Lake Macquarie, NSW, Australia, have been a historical source of selenium to the lake. Although dissolved selenium concentrations have been marginally elevated, sediments are the major sink. Methylation of sedimentary selenium to volatile dimethylselenide (DMSe) is known to be a natural remediation process. Sediments from north of Wyee Bay and the Vales Point Power Station were the subject of field sampling and monitoring to determine the extent to which selenium is being lost to the atmosphere as DMSe. Flux estimates were obtained by trapping volatile selenium species using benthic domes, followed by analysis in the field using a fully automated cryogenic trapping system with atomic fluorescence detection. The detection limit of the system was 0.1ngL–1 for DMSe and 1ngL–1 for dimethyl diselenide (DMDSe). Measurements in both summer and late autumn–early winter showed a distinct seasonal difference, with a higher summer DMSe flux of 53±25ng Se m–2h–1 (±s.d.) compared with 8±5ng Se m–2h–1 in late autumn–early winter. No DMDSe was detected. These fluxes are similar to those measured in Europe and North America, and represent an annual loss of 1.3kg of selenium per year from the nearby lake area. Lake-wide this would represent a significant loss to the atmosphere.

Quantification of methylated selenium, sulfur, and arsenic in the environment.

Biomethylation and volatilization of trace elements may contribute to their redistribution in the environment. However, quantification of volatile, methylated species in the environment is complicated by a lack of straightforward and field-deployable air sampling methods that preserve element speciation. This paper presents a robust and versatile gas trapping method for the simultaneous preconcentration of volatile selenium (Se), sulfur (S), and arsenic (As) species. Using HPLC-HR-ICP-MS and ESI-MS/MS analyses, we demonstrate that volatile Se and S species efficiently transform into specific non-volatile compounds during trapping, which enables the deduction of the original gaseous speciation. With minor adaptations, the presented HPLC-HR-ICP-MS method also allows for the quantification of 13 non-volatile methylated species and oxyanions of Se, S, and As in natural waters. Application of these methods in a peatland indicated that, at the selected sites, fluxes varied between 190–210 ng Se·m−2·d−1, 90–270 ng As·m−2·d−1, and 4–14 µg S·m−2·d−1, and contained at least 70% methylated Se and S species. In the surface water, methylated species were particularly abundant for As (>50% of total As). Our results indicate that methylation plays a significant role in the biogeochemical cycles of these elements.

Preconcentration and in-situ photoreduction of trace selenium using TiO2 nanoparticles, followed by its determination by slurry photochemical vapor generation atomic fluorescence spectrometry

We have developed a method for the determination of trace levels of total selenium in water samples. It integrates preconcentration, in-situ photoreduction and slurry photochemical vapor generation using TiO2 nanoparticles, and the determination of total selenium by AFS. The Se(IV) and Se(VI) species were adsorbed on a slurry of TiO2 nanoparticles which then were exposed to UV irradiation in the presence of formic acid to form volatile selenium species. The detection limits were improved 17-fold compared to hydride generation and 56-fold compared to photochemical vapor generation, both without any preconcentration. No significant difference was found in the limits of detection (LODs) for Se(IV) and Se(VI). The LOD is as low as 0.8 ng L−1, the precision is better than 4.5 % (at a level of 0.1 μg L−1 of selenium). The method gave good recoveries when applied to the determination of total selenium in a certified tissue reference material (DORM-3) and in spiked drinking water and wastewater samples containing high concentrations of transition and noble metal ions. It also excels by very low LODs, a significant enhancement of sample throughput, reduced reagent consumption and sample loss, and minimal interference by transition and noble metal ions.

Effective selenium volatilization under aerobic conditions and recovery from the aqueous phase by Pseudomonas stutzeri NT-I

Selenium is an important rare metal and its recovery from waste and wastewater is necessary for its sustainable utilization. Microbial selenium volatilization is suitable for selenium recovery from industrial wastewater because volatile selenium can be recovered in recyclable forms free from other chemicals. We found that Pseudomonas stutzeri NT-I can aerobically transform selenate, selenite, and biogenic elemental selenium into dimethyldiselenide as well as dimethylselenide; these were temporarily accumulated in the aqueous phase and then transferred into the gaseous phase. The rate of selenium volatilization using strain NT-I ranged 6.5–7.6 μmol/L/h in flask experiments and was much higher than the rates reported previously for other microbes. The selenium volatilization rate accelerated to 14 μmol/L/h in a jar fermenter. Furthermore, 82% of the selenium volatilized using strain NT-I was recovered with few impurities within 48 h in a simple gas trap with nitric acid, demonstrating that strain NT-I is a promising biocatalyst for selenium recovery through biovolatilization from the aqueous phase.

Real-Time Quantification of Traces of Biogenic Volatile Selenium Compounds in Humid Air by Selected Ion Flow Tube Mass Spectrometry

Biological volatilization of selenium, Se, in a contaminated area is an economical and environmentally friendly approach to phytoremediation techniques, but analytical methods for monitoring and studying volatile compounds released in the process of phytovolatilization are currently limited in their performance. Thus, a new method for real time quantification of trace amounts of the vapors of hydrogen selenide (H(2)Se), methylselenol (CH(3)SeH), dimethylselenide ((CH(3))(2)Se), and dimethyldiselenide ((CH(3))(2)Se(2)) present in ambient air adjacent to living plants has been developed. This involves the characterization of the mechanism and kinetics of the reaction of H(3)O(+), NO(+), and O(2)(+•) reagent ions with molecules of these compounds and then use of the rate constants so obtained to determine their absolute concentrations in air by selected ion flow tube mass spectrometry, SIFT-MS. The results of experiments demonstrating this method on emissions from maize (Zea mays) seedlings cultivated in Se rich medium are also presented.

Nanosemiconductor-Based Photocatalytic Vapor Generation Systems for Subsequent Selenium Determination and Speciation with Atomic Fluorescence Spectrometry and Inductively Coupled Plasma Mass Spectrometry

We reported novel Ag-TiO(2)- and ZrO(2)-based photocatalytic vapor generation (PCVG) systems as effective sample introduction techniques for further improving the sensitivity of the atomic spectrometric determination of selenium for the first time, in which the conduction band electron served as a "reductant" to reduce selenium species including Se(VI) and convert them directly into volatile H(2)Se, which was easily separated from the sample matrix and underwent more effectively subsequent atomization and/or ionization. These two PCVG systems helped us to overcome the problem encountered in the most conventional KBH(4)/OH(-)-H(+) system, in that Se(VI) was hardly converted into volatile selenium species without the aid of prereduction procedures. The limits of detection (LODs) (3σ) of the four most typical Se(IV), Se(VI), selenocystine ((SeCys)(2)), and selenomethionine (SeMet) species were, respectively, down to 1.2, 1.8, 7.4, and 0.9 ng mL(-1) in UV/Ag-TiO(2)-HCOOH, and 0.7, 1.0, 4.2, and 0.5 ng mL(-1) in UV/ZrO(2)-HCOOH with the relative standard deviations (RSDs) lower than 5.1% (n = 9 at 1 μg mL(-1)) when using atomic fluorescence spectrometry (AFS) under flow injection mode. They reached 10, 14, 18, and 8 pg mL(-1) in UV/Ag-TiO(2)-HCOOH, and 6, 7, 10, and 5 pg mL(-1) in UV/ZrO(2)-HCOOH with the RSDs lower than 4.4% (n = 9 at 10 ng mL(-1)) when using inductively coupled plasma mass spectrometry (ICPMS). After the two PCVG systems were validated using certified reference materials GBW(E)080395 and SELM-1, they were applied to determine the total Se in the selenium-enriched yeast sample and used as interfaces between high-performance liquid chromatography (HPLC) and AFS or ICPMS for selenium speciation in the water- and/or enzyme-extractable fractions of the selenium-enriched yeast.

Selenium speciation in flue desulfurization residues

Flue gas from coal combustion contains significant amounts of volatile selenium (Se). The capture of Se in the flue gas desulfurization (FGD) scrubber unit has resulted in a generation of metal-laden residues. It is important to determine Se speciation to understand the environmental impact of its disposal. A simple method has been developed for selective inorganic Se(IV), Se(VI) and organic Se determination in the liquid-phase FGD residues by hydride generation atomic fluorescence spectrometry (AFS). It has been determined that Se(IV), Se(VI) and organic Se can be accurately determined with detection limits (DL) of 0.05, 0.06 and 0.06 μg/L, respectively. The accuracy of the proposed method was evaluated by analyzing the certified reference material, NIST CRM 1632c, and also by analyzing spiked tap-water samples. Analysis indicates that the concentration of Se is high in FGD liquid residues and primarily exists in a reduced state as selenite (Se(IV)). The toxicity of Se(IV) is the strongest of all Se species. Flue gas desulfurization residues pose a serious environmental risk.

Study of volatile selenium metabolites stability in normal urine: effects of sample handling and storage conditions

The aim of this study was to define suitable conditions for sample handling and storage of urine samples in order to ensure reliable analysis of selenium-containing volatile metabolites. Short-term stability testing (from sample collection to 30–35 hours) included: temperature (room, i.e. 22 ± 2 °C, refrigerator (4 °C)), the presence and absence of light, and addition of a bactericide (0.05% NaN3). The long-term stability study evaluated urine storage at −20 and −80 °C over a period of 4 weeks. This work was conducted with normal urine samples, i.e. from non-supplemented human volunteers, in order to profile baseline metabolites and corresponding concentration levels. The results indicate that urine samples should be maintained in the dark immediately after collection and preferably analyzed within the day of collection. If temporary storage cannot be avoided, it should be at 4 °C after addition of NaN3. For longer period, urine samples can be stored at −20 or −80 °C without measurable changes respectively for 2 to 4 weeks.