Chemical fractionation and speciation modelling for optimization of ion-exchange processes to recover palladium from industrial wastewater.

Palladium is used in several industrial applications and, given its high intrinsic value, intense efforts are made to recover the element. In this hydrometallurgic perspective, ion-exchange (IEX) technologies are principal means. Yet, without incorporating the chemical and physical properties of the Pd present in real, plant-specific conditions, the recovery cannot reach its technical nor economic optimum. This study characterized a relevant Pd-containing waste stream of a mirror manufacturer to provide input for a speciation model, predicting the Pd speciation as a function of pH and chloride concentration. Besides the administered neutral PdCl2 form, both positively and negatively charged [PdCln](2-n) species occur depending on the chloride concentration in solution. Purolite C100 and Relite 2AS IEX resins were selected and applied in combination with other treatment steps to optimize the Pd recovery. A combination of the cation and anion exchange resins was found successful to quantitatively recover Pd. Given the fact that Pd was also primarily associated with particles, laboratory-scale experiments focused on physical removal of the Pd-containing flow were conducted, which showed that particle-bound Pd can already be removed by physical pre-treatment prior to IEX, while the ionic fraction remains fully susceptible to the IEX mechanism.

Waterborne versus dietary zinc accumulation and toxicity in Daphnia magna: a synchrotron radiation based X-ray fluorescence imaging approach.

Recent studies have suggested that exposure of the freshwater invertebrate Daphnia magna to dietary Zn may selectively affect reproduction without an associated increase of whole body bioaccumulation of Zn. The aim of the current research was therefore to investigate the hypothesis that dietary Zn toxicity is the result of selective accumulation in tissues that are directly involved in reproduction. Since under field conditions simultaneous exposure to both waterborne and dietary Zn is likely to occur, it was also tested if accumulation and toxicity under combined waterborne and dietary Zn exposure is the result of interactive effects. To this purpose, D. magna was exposed during a 16-day reproduction assay to Zn following a 5 × 2 factorial design, comprising five waterborne concentrations (12, 65, 137, 207, and 281 µg Zn/L) and two dietary Zn levels (49.6 and 495.9 µg Zn/g dry wt.). Tissue-specific Zn distribution was quantified by synchrotron radiation based confocal X-ray fluorescence (XRF). It was observed that the occurrence of reproductive inhibition due to increasing waterborne Zn exposure (from 65 µg/L to 281 µg/L) was accompanied by a relative increase of the Zn burdens which was similar in all tissues considered (i.e., the carapax, eggs, thoracic appendages with gills and the cluster comprising gut epithelium, storage cells and ovaries). In contrast, the impairment of reproduction during dietary Zn exposure was accompanied by a clearly discernible Zn accumulation in the eggs only (at 65 µg/L of waterborne Zn). During simultaneous exposure, bioaccumulation and toxicity were the result of interaction, which implies that the tissue-specific bioaccumulation and toxicity following dietary Zn exposure are dependent on the Zn concentration in the water. Our findings emphasize that (i) effects of dietary Zn exposure should preferably not be investigated in isolation from waterborne Zn exposure, and that (ii) XRF enabled us to provide possible links between tissue-specific bioaccumulation and reproductive effects of Zn.

Living in a transient world: ICP-MS reinvented via time-resolved analysis for monitoring single events.

After 40 years of development, inductively coupled plasma-mass spectrometry (ICP-MS) can hardly be considered as a novel technique anymore. ICP-MS has become the reference when it comes to multi-element bulk analysis at (ultra)trace levels, as well as to isotope ratio determination for metal(loid)s. However, over the last decade, this technique has managed to uncover an entirely new application field, providing information in a variety of contexts related to the individual analysis of single entities (e.g., nanoparticles, cells, or micro/nanoplastics), thus addressing new societal challenges. And this profound expansion of its application range becomes even more remarkable when considering that it has been made possible in an a priori simple way: by providing faster data acquisition and developing the corresponding theoretical substrate to relate the time-resolved signals thus obtained with the elemental composition of the target entities. This review presents the underlying concepts behind single event-ICP-MS, which are needed to fully understand its potential, highlighting key areas of application (e.g., single particle-ICP-MS or single cell-ICP-MS) as well as of future development (e.g., micro/nanoplastics).

Mass-independent isotope fractionation of heavy elements measured by MC-ICPMS: a unique probe in environmental sciences.

This article overviews recent developments in the use of multicollector inductively coupled plasma mass spectrometry (MC-ICPMS) in studies of mass-independent isotope chemistry of heavy elements. Origins of mass-independent isotope effects and their relevance to isotope ratio measurements by MC-ICPMS are briefly described. The extent to which these effects can affect instrumental mass bias in MC-ICPMS is critically discussed on the basis of the experimental observations. Furthermore, key findings reported in studies of mass-independent isotope fractionation (MIF) of mercury in the field of environmental sciences are reviewed. MIF of heavy elements is not only of interest from a fundamental point of view, but also provides scientists with a new and effective means of studying the biogeochemistry of these elements.

Isotopic evolution of planetary crusts by hypervelocity impacts evidenced by Fe in microtektites.

Fractionation effects related to evaporation and condensation had a major impact on the current elemental and isotopic composition of the Solar System. Although isotopic fractionation of moderately volatile elements has been observed in tektites due to impact heating, the exact nature of the processes taking place during hypervelocity impacts remains poorly understood. By studying Fe in microtektites, here we show that impact events do not simply lead to melting, melt expulsion and evaporation, but involve a convoluted sequence of processes including condensation, variable degrees of mixing between isotopically distinct reservoirs and ablative evaporation during atmospheric re-entry. Hypervelocity impacts can as such not only generate isotopically heavy, but also isotopically light ejecta, with δ56/54Fe spanning over nearly 5‰ and likely even larger variations for more volatile elements. The mechanisms demonstrated here for terrestrial impact ejecta modify our understanding of the effects of impact processing on the isotopic evolution of planetary crusts.

Multielement analysis of polyethylene using solid sampling electrothermal vaporization ICP mass spectrometry

Next to laser ablation (LA) also electrothermal vaporization (ETV) from a graphite furnace as a means of sample introduction opens possibilities for direct analysis of solid samples using inductively coupled plasma mass spectrometry (ICPMS). In this paper, it is demonstrated that solid sampling ETV-ICPMS is very well suited for the determination of metal traces in polyethylene. A limited multielement capability is often cited as an important drawback of ETV-ICPMS. However, by studying the effect of monitoring an increasing number of mass-to-charge ratios on the signal profile (integrated signal intensity and repeatability) of selected analyte elements, the multielement capability of (solid sampling) ETV-ICPMS was systematically evaluated, and the results obtained suggest that, with a quadrupole-based ICPMS instrument, at least 11 elements can be determined "simultaneously" (from the same vaporization step), in essence without compromising the sensitivity or the precision of the results obtained. In this work, the "simultaneous" determination of Al, Ba, Cd, Cu, Mn, Pb, and Ti in a polyethylene candidate reference material has been accomplished, despite the large variation in analyte concentration (from 5 ng/g for Mn to 500 microg/g for Ti) and in furnace behavior (volatility) they exhibit. To avoid premature losses of Cd during thermal pretreatment of the samples, Pd was used as a chemical modifier. Two different calibration methods--external calibration using an aqueous standard solution and single standard addition--were studied and the results obtained were compared with those obtained using neutron activation analysis (NAA) and/or with the corresponding (candidate) certified values (if available). Single standard addition was shown to be preferable (average deviation between ICPMS result and reference value < 3%), although--except for Ba--acceptable results could also be obtained with external calibration.

Non-spectral interferences encountered with a commercially available high resolution ICP-mass spectrometer.

Results of a systematic study concerning non-spectral interferences observed with a commercially available high resolution ICP-mass spectrometer are reported and compared to observations made with a quadrupole-based instrument. In general, matrix effects were observed to be to a large extent comparable for both instruments used. In all cases, the matrix-induced signal suppression or enhancement was seen to depend in a regular way on the mass number of the nuclides monitored. In most cases, the ionization potential of the nuclides has little or no influence on the extent of suppression or enhancement. For As, Se and Te, the introduction of 2.5% ethanol, 0.5 mol/l H(2)SO(4), or to a lesser extent 0.5 mol/l H(3)PO(4), leads to an exceptional increase in the signal intensity for both instruments. Registration of signal behaviour plots (signal intensity as a function of the nebulizer gas flow rate) in different matrices revealed that both the height of the plot and the optimum nebulizer gas flow rate are a function of the matrix composition. Finally, no indication was found that the acceleration of the extracted ions over 8000 V with the high resolution instrument would lead to an alleviation of space charge effects when compared to a quadrupole-based ICP-mass spectrometer.

The use of internal standards in ICP-MS.

Careful study of the matrix effect in ICP-MS showed that, in all cases studied, the magnitude of the signal suppression or enhancement depends in a regular way on the mass number. Hence, accurate correction for non-spectral interferences is only possible using an internal standard with mass number close to that of the analyte element(s). It is also shown that using an internal standard with mass number close to that of the analyte improves the precision. For both cases, the ionization energy of the internal standard seems to be of no or only secondary importance. To obtain optimal precision and accuracy, the internal standard should be selected as close in mass number as possible to that of the analyte element(s). When a number of elements over a considerable mass range are to be determined, several internal standards have to be used.

The determination of molybdenum in a sea water candidate reference material by inductively coupled plasma-mass spectrometry.

In the framework of a certification campaign organized by BCR (Bureau Communautaire de Référence, Commission of the European Communities, Brussels) molybdenum was determined in a sea water candidate reference material (BCR CRM 403) using inductively coupled plasma-mass spectrometry. The determination was hampered by both non-spectral (signal suppression) and spectral interferences. Ten-fold dilution of the sea water and the use of a carefully selected internal standard allowed accurate correction for the signal suppression. Spectral interferences on Mo nuclides could mainly be attributed to BrO(+) and BrOH(+) ions. At the level of spectral overlap encountered, these interferences could be corrected for with sufficient accuracy by matrix matching of the blank for Br or by application of a mathematical correction method involving resolvation of a pair of simultaneous equations. Results obtained after application of anion exchange to separate Br from Mo confirmed the results obtained using the correction methods, proving the validity of the latter. A good agreement is established by comparison of the ICP-MS result with those obtained by other techniques in other laboratories.

Reproductive toxicity of dietary zinc to Daphnia magna.

Regulatory assessments of metals in freshwaters are mostly based on dissolved metal concentrations, assuming that toxicity is caused by waterborne metal only. Little attention has been directed to the toxicity of dietary metals to freshwater invertebrates. In this study the chronic toxicity of dietary zinc to Daphnia magna was investigated. The green alga Pseudokirchneriella subcapitata was exposed for 64 h to a control and three dissolved zinc concentrations, i.e. 23, 28 and 61 microg L(-1), resulting in internal zinc burdens in the algae of 130, 200, 320 and 490 microg g(-1) dry weight, respectively. These algae were used as a food source in chronic, 21-day bioassays with D. magna in a test medium to which no dissolved zinc was added. None of the treatments resulted in effects on feeding rates or somatic growth of D. magna. In contrast, a significant 40% decrease of total reproduction (number of juveniles per adult) was observed in the 28 and 61 microg L(-1) treatments. Time to first brood was not affected, whereas the mean brood size and the fraction of reproducing parent daphnids were reduced from the second brood onwards and the magnitude of these reductions increased with each subsequent brood. The reduced reproduction was accompanied with an elevated zinc accumulation in the 61 microg L(-1) treatment only, suggesting that total body burden is no good indicator of dietary zinc toxicity. Overall our data suggest that dietary zinc specifically targets reproduction in D. magna through accumulation in particular target sites, possibly cells or tissues where vitellogenin synthesis or processing occur. Further, our data illustrate that the potential importance of the dietary exposure route should be carefully considered and interpreted in regulatory assessments of zinc.

Determination of the uptake of [Pt(NH3)4](NO3)2 by grass cultivated on a sandy loam soil and by cucumber plants, grown hydroponically.

Two cultivation experiments were carried out in order to answer the question to what extent platinum can enter the food chain by accumulation in plants, when the platinum is present in a bio-available form: (i) cucumber plants (Cucumis sativus) were grown hydroponically in nutrient solutions containing [Pt(NH3)4](NO3)2 (from 0.5 to 50 micrograms Pt/l solution); and (ii) a water-soluble platinum compound--[Pt(NH3)4](NO3)2--was added in increasing amounts to a sandy loam soil (from 0.5 to 50 mg Pt/kg soil) and rye grass (Lolium perenne) was grown on it. The roots on the one hand and the green plant fractions in the other hand of the cucumber plants and the rye grass were digested using a high-pressure asher. The platinum concentration was determined by means of a quadrupole-based (VG PQ I) or a double focusing sector field ICP-mass spectrometer (Finnigan MAT, Element), depending on the platinum concentration in the sample solution. The detection limit for platinum obtained with the VG PQ I was observed to be 6 ng/1, while with the 'Element' the detection limit could be improved to 0.5 ng/1 Pt. Accumulation factors were calculated as the ratio of the platinum concentration in the plant to that in the soil or the nutrient solution. The grass grown on spiked soil accumulated platinum only to a slight degree (accumulation factors between 0.008 and 0.032). The hydroponically grown cucumber plants, however, strongly accumulated it (accumulation factors of 11-42 in the shoot and 1700-2100 in the roots). There are three possible causes for the large differences in the accumulation factors: (i) Cucumber plants are dicotyledons; grass, however, is a monocotyledon. Other cultivation experiments already showed that dicotyledons accumulate metals to a higher extent than monocotyledons. (ii) In the grass cultivation experiment, the platinum compound was only added once to the sandy loam soil, namely 2 days before grass was cultivated on it. The nutrient solutions of the cucumber plants were changed twice a week. Consequently, the total amount of platinum that the plants were exposed to during the cultivation of the cucumber plants was higher than during the cultivation of the grass. (iii) Immobilization of the platinum compound in the soil most likely occurred.

Uptake of ingested uranium after low "acute intake".

The uptake of uranium, ingested as a soluble compound, was studied by monitoring the uranium level in urine by inductively coupled plasma mass spectrometry and through measurement of an isotopic tracer. The high sensitivity of this method allows measurement of uranium levels in urine samples from each voiding, therefore more detailed biokinetic studies are possible. To simulate low "acute intake," five volunteers with "normal" levels (5-15 ng L(-1)) of uranium in urine ingested a grapefruit drink spiked with 100 microg of uranium (235U/238U = 0.245%) as uranyl nitrate, and the level of uranium in their urine after ingestion was monitored. Two techniques were applied to estimate the extent of exposure: a) uranium levels above the normal level for each volunteer; and b) the deviation from natural isotopic ratio. Results were normalized relative to the creatinine concentration, which served as an indicator of urine dilution, to reduce effects due to diurnal changes. The results clearly indicate that currently accepted bio-kinetic models overestimate the time between ingestion of dissolved uranium and its excretion in urine, the maximum of which was found to be around 6-10 h. The uptake fraction was in agreement with recent studies, i.e., 0.1-0.5% of the ingested uranium for four of the subjects but above 1.5% for the fifth, and well below the 5% reported in International Commission on Radiation Protection Publication 54. Finally, partial results from the isotope dilution study indicate that uranium absorbed through the intestine interchanges with uranium retained in body organs. The time scale of this process is quite short, and the acute exposure led to a minimum in the isotopic ratio within hours, while recovery back to natural abundance due to low chronic exposure takes several days.

Intraregional classification of wine via ICP-MS elemental fingerprinting.

The feasibility of elemental fingerprinting in the classification of wines according to their provenance vineyard soil was investigated in the relatively small geographical area of a single wine district. Results for the Stellenbosch wine district (Western Cape Wine Region, South Africa), comprising an area of less than 1,000 km(2), suggest that classification of wines from different estates (120 wines from 23 estates) is indeed possible using accurate elemental data and multivariate statistical analysis based on a combination of principal component analysis, cluster analysis, and discriminant analysis. This is the first study to demonstrate the successful classification of wines at estate level in a single wine district in South Africa. The elements B, Ba, Cs, Cu, Mg, Rb, Sr, Tl and Zn were identified as suitable indicators. White and red wines were grouped in separate data sets to allow successful classification of wines. Correlation between wine classification and soil type distributions in the area was observed.

Enzymatic mineralization of gellan gum hydrogel for bone tissue-engineering applications and its enhancement by polydopamine.

Interest is growing in the use of hydrogels as bone tissue-engineering (TE) scaffolds due to advantages such as injectability and ease of incorporation of active substances such as enzymes. Hydrogels consisting of gellan gum (GG), an inexpensive calcium-crosslinkable polysaccharide, have been applied in cartilage TE. To improve GG suitability as a material for bone TE, alkaline phosphatase (ALP), an enzyme involved in mineralization of bone by cleaving phosphate from organic phosphate, was incorporated into GG hydrogels to induce mineralization with calcium phosphate (CaP). Incorporated ALP induced formation of apatite-like material on the submicron scale within GG gels, as shown by FTIR, SEM, EDS, XRD, ICP-OES, TGA and von Kossa staining. Increasing ALP concentration increased amounts of CaP as well as stiffness. Mineralized GG was able to withstand sterilization by autoclaving, although stiffness decreased. In addition, mineralizability and stiffness of GG was enhanced by the incorporation of polydopamine (PDA). Furthermore, mineralization of GG led to enhanced attachment and vitality of cells in vitro while cytocompatibility of the mineralized gels was comparable to one of the most commonly used bone substitute materials. The results proved that ALP-mediated enzymatic mineralization of GG could be enhanced by functionalization with PDA.

Determination of elemental impurities in leachate solutions from syringes using sector field ICP-mass spectrometry.

Prefilled syringes are of increasing importance on the drug product market. Drug products supplied in prefilled syringes have to comply with guidelines on elemental impurity limit concentrations. Elemental impurities may be introduced through any reagents or catalysts used or any product contact surface. This work addresses the determination of elemental impurities leaching from three types of glass syringe container-closure systems supplied by two leading manufacturers. Leachate solutions of every type of syringe were analyzed for Na, Al, Si, W and the 16 elements listed in draft USP chapter 232, which were selected on grounds of toxicity. Elemental impurity concentrations were determined using sector field ICP-mass spectrometry. Significant concentrations of Na and Si were found in all leachate solutions, up to 1200 and 4500µgL(-1), respectively. In addition, also Al, As and W were leached out of syringes from one manufacturer in variable amounts, giving rise to average concentrations (std. dev., n=6) of 400 (120), 0.55 (0.08) and 230 (220)µgL(-1), respectively. So far, no exceeding of limit concentrations was observed.

Laser ablation single-collector inductively coupled plasma mass spectrometry for lead isotopic analysis to investigate evolution of the Bilbilis mint.

This work explores the performance of laser ablation-inductively coupled plasma mass spectrometry using different types of single-collector devices (sector field and time-of-flight instrumentation) for lead isotopic analysis of bronze coins, minted in the ancient city of Bilbilis. The aim of the study was achieving sufficient discrimination power to reveal similarities and differences for coins originating from different historical periods, and to obtain information on the possible source of the lead ores used in their production, while restricting the damage inflicted to the samples such that it is not visible to the naked eye. It was found that satisfactory results (RSD in the 0.15-0.30% range for (207)Pb/(206)Pb and (208)Pb/(206)Pb ratios) could be finally obtained, despite the noisy nature of signals generated upon ablation of the highly inhomogeneous coins, by means of a methodology based on: (a) selection of the line profiling ablation mode; (b) use of a dual pass spray chamber that permits the simultaneous introduction of a solution (containing thallium of known isotopic composition), thus resulting in a wet plasma that showed an increased robustness towards matrix effects and (c) detection using a TOF-ICPMS unit, which proved to be much better suited to deal with the transient signals obtained, while being also sufficiently sensitive to obtain good counting statistics, owing to the high lead level (average around 5%) present in the samples. Moreover, under these conditions, the simultaneous aspiration of the thallium spike permitted accurate correction for mass discrimination, such that it was not necessary to use external matrix-matched standards for calibration.

Isotopic fractionation of Sn during methylation and demethylation reactions in aqueous solution.

Laboratory experiments, modeling the methylation of inorganic Sn(II) by methylcobalamin and the decomposition of methyltin under irradiation with UV light in aqueous solution, have been performed. Methyltin has been separated from inorganic Sn using anion-exchange chromatography and subjected to Sn isotope ratio measurements via solution nebulization multicollector inductively coupled plasma mass spectrometry (MC-ICPMS). The methylation of Sn(II) in the dark was accompanied by mass-dependent Sn isotopic fractionation, which resulted in preferential partitioning of the lighter Sn isotopes into the organic phase, with a shift of approximately 0.57 +/- 0.12 per thousand in terms of delta124/ 116Sn between methylated and inorganic Sn. The methylation of Sn(II) by methylcobalamin under UV irradiation resulted in the accelerated formation of methyltin in the beginning of the process, but was followed by the photolytic degradation of methyltin until its complete mineralization. The photolytic degradation of methyltin in the presence of methylcobalamin and inorganic Sn(II) was slower than that of pure solutions of commercially obtained monomethyltin. This is attributed to the methylating action of methyl radicals produced from photolytically decomposing methylcobalamin. Both synthesis and decomposition of methyltin under UV irradiation were accompanied by both mass-dependent and mass-independent Sn isotopic fractionation, with the latter due to the magnetic isotope effect. As a result of this, the lighter Sn isotopes preferentially partition into reaction products, while the odd isotopes, 117Sn and 119Sn, are selectively enriched relative to the other isotopes in the starting molecules. The extent of the observed variations in the isotopic composition of Sn is larger than that documented previouslyfor geological and archeological samples. These results indicate that Sn isotopic fractionation between various chemical forms of Sn in the natural aquatic systems may be significant and can provide new insights into the biogeochemical cycling of the element.

Urban/peri-urban aerosol survey by determination of the concentration and isotopic composition of Pb collected by transplanted lichen Hypogymnia physodes.

In the northeastern part of France, around the city of Metz, lichens (Hypogymnia physodes) have been transplanted from a single reference site to five different sites: (i) the reference site itself, (ii and iii) two peri-urban sites, (iv) a site in the proximity of a highway, and (v) a final one close to an industrial site. The dynamics of two different system set-ups (one covered and one uncovered) were evaluated. Samples have been collected 14, 34, and 68 days after transplantation. Lead concentrations already accumulated in the thallus, and the corresponding Pb isotopic compositions have been measured by quadrupole-based ICP-mass spectrometry. A systematic difference between the two setups is found for Pb concentrations, with the higher concentrations measured in lichens from the uncovered devices. Lead concentrations in lichens from the covered devices were found to be lower than or equal to the original concentration. Also the Pb isotopic compositions show a systematic difference between the devices, with the Pb isotopic composition present in lichens from the uncovered device being more radiogenic. Substantial changes in the isotopic composition of Pb are recorded for lichens from the uncovered device (from about 1.15 up to 1.22 for the 206Pb/207Pb ratio), in some cases already after only 34 days of exposure. The increases in the Pb concentration and the 206pb/207Pb ratio and the differences between the devices are explained by hypothesizing that (i) different Pb sources give rise to a different size distribution of aerosol particles and (ii) in the lichens present in the covered setup, a part of the aerosol particles cannot be incorporated. Also the influence of the source of the aerosols to lichens after transplantation is evaluated and the potential influence of biological reactions is discussed.

Characterization of cobalt pigments found in traditional Valencian ceramics by means of laser ablation-inductively coupled plasma mass spectrometry and portable X-ray fluorescence spectrometry.

In this work, a comparison of the performances of laser ablation-inductively coupled plasma mass spectrometry (LA-ICPMS) and portable X-ray fluorescence (XRF) spectrometry for the characterization of cobalt blue pigments used in the decoration of Valencian ceramics is presented. Qualitative data on the elemental composition of the blue pigments obtained using both techniques show a good agreement. Moreover, the results clearly illustrate that potters utilized different kinds of cobalt pigments in different historical periods. While both techniques seem suitable for the proposed task, they show different strengths and weaknesses. Portable X-ray fluorescence spectrometry is a cheaper and totally non-destructive technique, capable of providing fast and reliable results at the mgg(-1) level. LA-ICPMS, on the other hand, offers a much higher detection power and better spatial resolution, but its use results in some sample damage (sample consumption at the mug level), while it is a more expensive and non-portable technique.