Search Results (52)

The Dajing Cu-Sn polymetallic deposit, situated within the southern Great Xing’an Range of northern China, is a representative Mesozoic magmatic–hydrothermal system within a major Cu–Sn–Ag–Pb–Zn metallogenic belt. Located at the junction between the Siberian and North China plates, the deposit occurs within a composite tectonic domain overprinted by the Paleo-Asian, Mongol–Okhotsk, and Paleo-Pacific systems. Building on field geological constraints and detailed ore petrography, this study utilizes SEM–CL imaging and in situ LA–ICP–MS trace-element analysis of hydrothermal quartz to reconstruct the multistage physicochemical evolution and fluid dynamics of the ore-forming system. Three quartz generations record successive mineralization stages: early QI forms grain cores associated with Stage I cassiterite–arsenopyrite–quartz mineralization; main-stage QII crystallized during or shortly after Stage II chalcopyrite precipitation and exhibits well-developed oscillatory zoning; and late QIII occurs mainly as rim overgrowths and fracture fillings and postdates Stage III ore-mineral precipitation. Quartz is characteristically Ti-poor (4.7–22.8 ppm), and its trace-element systematics indicate a low- to intermediate-temperature hydrothermal signature and a granitic magmatic–hydrothermal affinity. Al, Li, Na, K, and Ge show coupled behavior consistent with heterovalent substitution and vary markedly among quartz generations, with CL-bright QIIa showing relatively higher Al, Ge, and Na relative to CL-dark QIIb, whereas QIII is generally characterized by lower Al, Li, and Ge. Localized anomalously high Cu and Sn values are mainly attributed to the co-ablation of fine-grained mineral inclusions, metal-rich fluid inclusions, or fracture-filling components. These features indicate a chemically heterogeneous fluid reservoir with inferred relatively acidic conditions during the initial Sn-mineralization stage. The fluid system subsequently experienced recurrent physicochemical fluctuations associated with pulsed fluid input during the principal Cu-mineralization stage. QIII records a trace element-depleted late-fluid system associated with the terminal pyrite–quartz stage. Late fluids migrated along earlier quartz boundaries and fractures and may have undergone further cooling and dilution through fluid mixing and/or water–rock interaction. Overall, the fluid system shows a progressive shift in inferred fluid chemistry, consistent with decreasing acidity during hydrothermal evolution. Full article

The origin of Mesozoic granites associated with the Dahutang W-Cu-Mo orefield in northern Jiangxi, which hosts the world’s second-largest tungsten deposit, remains a compelling subject despite extensive geochemical and geochronological studies. In this contribution, we present wolframite mineral and whole-rock geochemistry, as well as monazite and zircon U-Pb ages, for the Mesozoic granites to constrain our understanding of the petrogenesis of these granites and their coupling relationship with the mineralization. The following two magmatic phases and four types of rocks in the study area are identified: the early stage (152–147 Ma) biotite (G1) granites and the late stage (144–130 Ma) two-mica (G2),muscovite (G3), and albite (G4) granite series. These two magmatic phases are temporally coincident with two mineralization stages (~150 Ma and 144–139 Ma). All the Mesozoic granites share the characteristics of high silica content, peraluminosity (A/CNK > 1.1), and low Zr + Nb + Ce + Y values (<200 ppm); they are derived from the partial melting of a Proterozoic crustal source and classified as S-type granites. Specifically, the G1 granites are characterized by relatively high MgO (~0.5%), CaO (~1%), and low P₂O₅ (0.13%–0.20%). They formed through a relatively high degree of partial melting at approximately 766 °C (zircon saturation temperatures), a process influenced by biotite dehydration reactions, with minor contributions from mantle-derived materials. In contrast, the G2–G4 granite series exhibits more typical peraluminous S-type granite features, such as high Al₂O₃, Na₂O, and P₂O₅ (mostly > 0.2%) contents, and low Sr and Ba contents. They are products of low-degree partial melting that occurred under conditions close to muscovite breakdown at ~726 °C. Additionally, fluid–melt interaction is recorded in both granites by distinctive geochemical signatures, including enrichment in Sn (>30 ppm), Cs (>35 ppm), Li (>250 ppm), F (>0.4%), and W (10–1000 ppm), coupled with low K/Rb (<150) and Nb/Ta (<5) ratios. The near-chondritic Zr/Hf (22.6–34.1) and Y/Ho (24.5–31.5) ratios of the G1 granites imply a relatively limited role of magmatic fluid–melt interaction during its evolution. For the G2–G4 granites, however, intense crystal fractionation and late-stage fluid–melt interaction are well-documented by their highly variable and low ratios of Y/Ho (14.8–41.4), Nb/Ta (0.89–5.57), Zr/Hf (8.84–41.67), and K/Rb (13.96–128.29). In the long-lived, reduced, and volatile-rich aqueous environment of the G2–G4 magmas, fractional crystallization and albitization collectively enhanced the solubility and hydrothermal transport capacity of W, Sn, Li, Nb, and Ta by multiple orders of magnitude. In contrast, in the earlier, more oxidized G1 magmas (which incorporated mantle materials), the exsolution and hydrothermal transport of Cu and Mo were associated with localized greisenization, but their capacity diminished with fractional crystallization. Historically, mineral exploration in the Dahutang mining area has focused primarily on W, Cu, and Mo. Based on this research, we conclude that there is significant mineral potential for rare metals (particularly Sn, Li, and Ta), and future exploration should prioritize areas adjacent to the evolved G2–G4 peraluminous leucogranites to search for new concealed mineral occurrences. Full article

The aim of this study is to determine the spatial distribution of geochemical anomalies of selected potential toxic elements in the soils of the river basins in the Northeastern Caucasus—specifically the Ulluchay, Sulak, and Sunzha Rivers. A concentration of 25 chemical elements was measured using inductively coupled plasma mass spectrometry (ICP-MS). Petrogenic elements commonly found in the Earth’s crust (Al, Na, Ca, Fe, Mg) showed high concentrations (Na up to 306,600.70 mg/kg). Conversely, concentrations of Ag, Cd, Sn, Sb, and Te at many sampling sites were extremely low, falling below the detection limits of analytical instruments. The geochemical indicators Cf (contamination factor) and Igeo (geoaccumulation index) indicate that the regional characteristics of the territory, such as lithological conditions, hydrochemical schedules, and the history of geological development of the territory, affect the concentration of elements. Anomalous concentrations were found for seven elements (Ba, Na, Zn, Ag, Li, Sc, As), whereas no anomalies were identified for Be, Mg, Al, Mn, Fe, Co, Ni, Cu, Pb, Te, and Cs. For the most part (8 of 10), the sampling sites with anomalous chemical element content are located in the basin of the Sunzha River. Two sites with anomalous chemical element content have been identified in the Sulak River Basin. Anomalous values in the Sulak River Basin are noted for two chemical elements—Ba and Na. Natural features such as geological structure, parent rock composition, vertical climatic zonation, and landscape diversity play a major role in forming geochemical anomalies. The role of anthropogenic factors increases in localized areas near settlements, industrial facilities, and roads. The spatial distribution of geochemical anomalies must be considered in agricultural management, the use of water sources for drinking supply, the development of tourist routes, and comprehensive spatial planning. Full article

Current electrolytic refining processes for crude solder commonly employ fluosilicic acid (H₂SiF₆) as the electrolyte with bone glue and β-naphthol additives yet suffer from poor electrolyte stability, coarse cathode crystallization, low current efficiency, and high energy consumption, adversely affecting product quality and economic viability. In order to solve these limitations, electrochemical techniques, XRD, SEM, and ICP-OES were used to study the effects of gelatin and sodium lignosulfonate on the deposition overpotential and cathode morphology, as well as the effects of process parameters on current efficiency and energy consumption. A novel approach was developed using an H₂SiF₆ system enhanced by gelatin and sodium lignosulfonate for crude solder refining. After optimization, 120 h electrolysis achieved a current efficiency >97.8%, smooth/dense cathode surface, average cell voltage of 0.24 V, and energy consumption of 98.15 kWh/t. Efficient deposition of 81.2% Sn and 75.2% Pb on the cathode was realized, while >93.3% of Sb, Bi, Ag, Cu, and As were enriched in anode slime to facilitate valuable metal recovery, and >90.6% of In/Al concentrated in the electrolyte enabled effective Sn-Pb impurity separation. This study provides theoretical and technical foundations for advancing sustainable and economical electrolytic refining of crude solder. Full article

Background: Foods containing nutraceuticals from the mineral element group are being developed to compensate for the problem of deficiency in billions of people around the world. This research focuses on essential elements of patented cereal-based mixtures to complement the deficiencies of these elements and, at the same time, assesses their safety in terms of toxic elements in the human diet. Methods: The mineral and trace element contents in the mixtures were determined using the ICP-MS method with a subsequent evaluation of the contributions of the mixtures to the essential and toxic reference values based on dietary intakes and exposures for adults at 60, 80 and 100 kg of adult body weight and a portion size of 50 g. The potential health risk was evaluated using a metal pollution index. Results: The concentrations of minerals and trace elements in the cereal-based mixtures analyzed were as follows: K (up to 4150 µg/g) ≥ P > Mg > Ca > Na > Fe > Zn > Mn > Cu > Al > Ba (up to 4.40 µg/g) > Sr (up to 480 ng/g) ≥ Ti ≥ Ni > Ce ≥ Co > As ≥ Cs > Ag ≥ Li > Se > Be > Cr > Tl > Pb ≥ Hg > Ho > Cd > Sn (up to 1.12 ng/g). The mixtures contribute significantly to the reference values for Mn, Cu, Zn, Fe, and P for adults. Individual dietary exposure values of toxic elements for adults weighing 60 kg decrease in this order: Al (10.1 µg/kg bw/day) > Ni (362 ng/kg bw/day) > As ≥ Pb > Ag > Hg > Cd > and Sn (0.93 ng/kg bw/day). Conclusions: In terms of Regulation (EU) No 1924/2006 of the European Parliament and of the Council on nutrition and health claims made on foods, the cereal-based mixtures could be labelled “source of” Mn, Cu, Zn, Fe, and P when their contributions to the reference values exceeded 15%; in addition, “low sodium/salt” or “very low sodium/salt” can be applied. The mixtures contribute insignificantly to the toxic reference values of Al, Sn, Hg, Cd, Ni, and Ag, and the exposure values of Pb for developmental neurotoxicity, nephrotoxicity, and cardiovascular effects were considered safe. Regarding the metal pollution index of mixtures, there is no concern for potential health effects. Cereal-based mixtures are suitable for use in the food industry as a potential source of beneficial micronutrients for the human diet, although bioaccessible studies should not be neglected. Full article

Osteoporosis is a major public health concern, particularly among postmenopausal women. Environmental exposure to metals has been proposed as a potential contributor to osteoporosis, but human data remain limited and inconsistent. This study investigated changes in urinary concentrations of 20 metal(loid)s in patients with osteoporosis, as well as the association of these elements with bone mineral density (BMD), in a cohort of 380 postmenopausal women aged 50–70 years from Cascavel, Paraná, Brazil. Demographic, lifestyle, and clinical data were collected, and urinary concentrations of aluminum (Al), barium (Ba), cadmium (Cd), cobalt (Co), cesium (Cs), copper (Cu), mercury (Hg), lithium (Li), manganese (Mn), molybdenum (Mo), nickel (Ni), lead (Pb), rubidium (Rb), antimony (Sb), selenium (Se), tin (Sn), strontium (Sr), thallium (Tl), uranium (U), and zinc (Zn) were measured by inductively coupled plasma mass spectrometry. BMD was assessed at the lumbar spine, femoral neck, and total hip using dual-energy X-ray absorptiometry. Osteoporosis was diagnosed in 73 participants (19.2%). Osteoporotic women had significantly higher urinary concentrations of Cd, Mn, Pb, Sb, Sn, and Zn (p < 0.05). Statistically significant negative correlations were observed between BMD and urinary concentrations of Al, Cd, Hg, Mn, Sb, and U. After adjustment for confounders, elevated urinary concentrations of Cd, Mn, Pb, and Sb remained independently and significantly associated with higher odds of osteoporosis, with Cd (aOR = 1.495; p = 0.026) and Sb (aOR = 2.059; p = 0.030) showing the strongest associations. In addition, women with urinary concentrations above the 90th percentile for both Cd and Sb had a significantly higher prevalence of osteoporosis compared to those with lower levels (44.4% vs. 18.0%; p = 0.011). Longitudinal studies are needed to confirm causality and inform prevention strategies. Full article

Leachates from electronic waste, slag dusts generated during the processing of electronic waste, sweeping jewelry, and municipal solid-waste incineration residues contain a myriad of base metals, such as aluminum (Al: 10–2000 mg/L), copper (Cu: 10–1000 mg/L), iron (Fe: 10–500 mg/L), nickel (Ni: 0.1–500 mg/L), lead (Pb: 1–500 mg/L), tin (Sn: 1–100 mg/L), and zinc (Zn: 5–500 mg/L), which are present at much higher quantities than Au (0.01–10 mg/L), which raises several drawbacks to the efficient recycling of Au with high purity using hydrometallurgical strategies. The aim of this work was to study the efficiency and selectivity of two strong basic anion exchange (DOW^TM XZ-91419.00 and Purogold^TM A194) resins to recover Au from a chloride multi-metal solution containing these metals. For both resins, the adsorption kinetic and equilibrium parameters for Au(III), determined at 1.12 mol/L HCl, Eh = 1.1 V, and 25 °C, proceeded according to a pseudo-second order and a Langmuir isotherm (qmax was 0.94 and 1.70 mmol/g for DOW^TM XZ-91419.00 and Purogold^TM A194 resins, respectively), respectively. Continuous adsorption experiments of Au (48 µmol/L; 2.0%) from a chloride multi-metal solution evidenced high Au retention capacity and selectivity to Au over Al, Cu, Fe, Ni, and Zn but low selectivity to Au over Ag and Sn for both resins. Concentrated (>3.3 mmol/L) and pure (>94%) Au eluates were obtained for both resins. Full article

This paper evaluates the possibility of analyzing the composition of high-quality copper scrap with X-ray fluorescence spectrometry (XRF) instead of electrogravimetry combined with flame atomic absorption spectroscopy (EG+FAAS) method. The evaluation of the methods was performed on three real copper scraps, the composition of which were estimated in average samples taken after re-melting. Traceability of XRF results was ensured by the use of new certified reference materials (CRMs) dedicated to copper scrap analysis. The copper content results obtained by XRF were characterized by high agreement with the reference results obtained by EG+FAAS method. The estimated expanded uncertainty for Cu of both methods was 0.23%. In addition to significant time savings without compromising accuracy, the XRF method additionally provided information on the content of 12 other elements, such as Sn, Zn, Co, Cd, Sb, Ni, Fe, Pb, Bi, Ag, Al, and P. This may make the XRF method attractive compared to the commonly used EG+FAAS method. Full article

The current development of soldering materials focuses on the properties of the solder itself, while the reliability of the joints formed after soldering is evaluated to a lesser extent. It is essential to understand the relationship between the structure and the strength of the solder joint obtained. This article shows that the properties of the material used for soldering only to a certain extent largely translate into the mechanical properties of the joint. The aim of this article is to emphasize the importance of the problem of the selection of the chemical composition of the solder with the simultaneous selection of the parameters of the soldering process, including the width of the solder gap for the selected strength properties of the connection. The purpose of this article is to emphasize that the selection of a chemical composition solder with a simultaneous selection of parameters of the soldering process, including the dimensions of the gaps of the soldered materials, are affected properties of the soldered joint. In this article, the main importance was focused on the chemical composition of a tin-based solder. The influence was analyzed, and the most favorable content of elements, such as Al and Cu, which create intermetallic phases, strengthening the soldered joint, was determined. The properties of the newly developed solder joint for alternator applications due to the specified conditions of the soldering process, including the width of the solder gap permissible for alternators, ensured the correct connections, the strength properties of which differed despite the use of the same soldering material and substrate material, as well as the soldering time and tip temperature. This article presents a change in the cracking model of a solder joint made using a newly developed material due to the width of the permissible solder gap in the production process of alternators. Full article

The aim of the present study was to evaluate the contamination state of the surface soil from 10 parks from Galati, Romania, and the health hazards of the soil. The soil samples, collected in each site from the playing ground and from the edge of the park, were analyzed by using combined Wavelength- (WDXRF) and Energy-Dispersive (EDXRF) X-ray fluorescence techniques. A total number of 27 chemical elements (Ag, Al, As, Ba, Ca, Cd, Cr, Co, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Ti, V, Zn and Zr) were quantified in the urban soils, and the results were compared to the normal and alert values from Romanian legislation for toxic trace elements, as well as with European and world average values of element concentrations. The mineralogical analyses were performed by Scanning Electron Microscopy with Energy-Dispersive X-ray Analysis (SEM-EDX) and the Attenuated Total Reflectance–Fourier Transform Infrared technique (ATR-FTIR). To assess the soil contamination and the impact on human health of the presence of potential toxic elements and heavy metals in the soil, a series of pollution and health risk indices were used. All the results indicated an unpolluted to moderately polluted soil. The soil samples collected from the edge of the parks presented higher values for the specific pollutants, which originated from heavy traffic, such as Cu, Cr, Zn and Pb. The non-carcinogenic and carcinogenic risk to children was assessed using estimated daily intake (EDI) in relation to the pathways whereby pollutants can enter the human body, such as ingestion, dermal contact, inhalation and vaporization. Using the obtained values for EDI, the hazard quotient and hazard index were determined, which strengthen the formerly issued presumption that soil pollution is moderate and, by itself, does not present any threat to children’s health. Full article

Knowledge about determinants of addiction in people taking addictive substances is poor and needs to be supplemented. The novelty of this paper consists in the analysis of innovative aspects of current research about relationships between determinants of addiction in Polish patients taking addictive substances and rare available data regarding the relationships between these factors from studies from recent years from other environments, mainly in Europe, and on the development of genetic determinants of physiological responses. We try to explain the role of the microelements Mn, Fe, Cu, Co, Zn, Cr, Ni, Tl, Se, Al, B, Mo, V, Sn, Sb, Ag, Sr, and Ba, the toxic metals Cd, Hg, As, and Pb, and the rare earth elements Sc, La, Ce, Pr, Eu, Gd, and Nd as factors that may shape the development of addiction to addictive substances or drugs. The interactions between factors (gene polymorphism, especially ANKK1 (TaqI A), ANKK1 (Taq1 A-CT), DRD2 (TaqI B, DRD2 Taq1 B-GA, DRD2 Taq1 B-AA, DRD2-141C Ins/Del), and OPRM1 (A118G)) in patients addicted to addictive substances and consumption of vegetables, consumption of dairy products, exposure to harmful factors, and their relationships with physiological responses, which confirm the importance of internal factors as determinants of addiction, are analyzed, taking into account gender and region. The innovation of this review is to show that the homozygous TT mutant of the ANKK1 TaqI A polymorphism rs 1800497 may be a factor in increased risk of opioid dependence. We identify a variation in the functioning of the immune system in addicted patients from different environments as a result of the interaction of polymorphisms. Full article

Intermetallic compounds (IMCs) growth can simultaneously bring about low-resistance electrical pathways and drastically reduce joint lifetime. Recently, incorporated trace nanoparticles into the free-Pb solder were found to promote the performance of the solder joints. Sn3Ag0.9Zn (SAZ) nano-composite solders were developed by doping 0.5 wt.% Al₂O₃ nanoparticles into the SAZ solder. The IMCs formation and growth behavior at the interfacial reactions between the SAZ-0.5Al₂O₃ nano-composite solder and the Cu substrate during soldering at temperatures ranging from 250 to 325 °C for 30 min were investigated. The results showed that after the addition of Al₂O₃ nanoparticles into the SAZ solder, the elongated-type IMCs layer changed into a prism-type IMCs layer, and Ag₃Sn nanoparticles were absorbed on the grain surface of the interfacial Cu₆Sn₅ phase, effectively suppressing the growth of the IMCs layers. The activation energies (Q) for the IMCs layers (Cu₆Sn₅ + Cu₃Sn) were determined to be 36.4 and 39.1 kJ/mol for the SAZ/Cu and SAZ-Al₂O₃/Cu solders, respectively. Full article

This study investigates the application of the vertical zone refining process to produce ultra-high-purity tin. Computational fluid dynamics (CFD) simulations were conducted using an Sn-1 wt.%Bi binary alloy to assess the effects of two key parameters—heater temperature and pulling rate—on Bi impurity segregation. The simulations revealed a dynamic evolution in molten zone height, characterized by an initial rapid rise, followed by a gradual increase and ending with a sharp decline. Despite these fluctuations, the lower solid–liquid interface consistently remained slightly convex. After nine zone passes, impurities accumulated at the top of the sample, with dual vortices forming a rhombus- or gate-shaped negative segregation zone. The simulations demonstrated that lower heater temperatures and slower pulling rates enhanced impurity segregation efficiency. Based on these results, experiments were performed using 6N-grade tin as the starting material. Glow discharge mass spectrometry (GDMS) analysis showed that the effective partition coefficients (k_eff) for impurities such as Ag, Pb, Co, Al, Bi, Cu, Fe, and Ni were significantly less than 1, while As was slightly below but very close to 1, and Sb was above 1. Under optimal conditions—405 °C heater temperature and a pulling rate of 5 μm/s—over 60% of impurities were removed after nine zone passes, approaching 6N9-grade purity. These findings provide valuable insights into optimizing the vertical zone refining process and demonstrate its potential for achieving 7N-grade ultra-high-purity tin. Full article

Posidonia oceanica significantly contributes to the health of oceans and coastal areas; however, its progressive decline is becoming an increasing source of concern. The present preliminary study aims to assess the chemical parameters that describe the state of preservation of the aforementioned plant meadows located in the Tremiti Islands archipelago. To better understand the plants’ response to external factors, the emission of biogenic volatile organic compounds (BVOCs) was investigated using Posidonia oceanica as a biological indicator. Subsequently, the heavy metal concentrations (Ag, Al, As, Ba, Be, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Sb, Se, Sn, Ti, Tl, V, Zn) in sediments, leaves, and seawater were determined and pollution indicators were calculated to assess the deviation from the natural background levels of sediments. The dimethyl sulfoniopropionate (DMSP) to dimethyl sulfoxide (DMSO) ratio was calculated to evaluate the oxidative stress levels in the meadows because the DMSP naturally present in Posidonia oceanica is oxidized to DMSO and decreases the ratio of DMSP/DMSO. BVOC analysis revealed dimethyl sulphide (DMS) as the most abundant molecule. Morphological features led to variations in metal concentrations across sampling sites, with sheltered bays displaying a higher metal content. Degradation is indicated by a greater DMSO content in the outer leaves. In accordance with the metal content, the bioindicator ratio confirms greater degradation on the south side, which aligns with increased oxidative stress. Full article

Printed circuit boards (PCBs) are the main components of e-waste. In order to reduce the negative impact of waste PCBs on human health and the environment, they must be properly disposed of. A new method is demonstrated for recycling waste PCBs. It is referred to as the high-temperature thermo-mechano-chemical gasification (TMCG) of PCBs by the detonation-born gasification agent (GA), which is a blend of H₂O and CO₂ heated to a temperature above 2000 °C. The GA is produced in a pulsed detonation gun (PDG) operating on a near-stoichiometric methane–oxygen mixture. The PDG operates in a pulsed mode producing pulsed supersonic jets of GA and pulsed shock waves possessing a huge destructive power. When the PDG is attached to a compact flow reactor filled with waste PCBs, the PCBs are subject to the intense thermo-mechano-chemical action of both strong shock waves and high-temperature supersonic jets of GA in powerful vortical structures established in the flow reactor. The shock waves grind waste PCBs into fine particles, which undergo repeated involvement and gasification in the high-temperature vortical structures of the GA. Demonstration experiments show full (above 98%) gasification of the 1 kg batch of organic matter in a setup operation time of less than 350 s. The gaseous products of PCB gasification are mainly composed of CO₂, CO, H₂, N₂, and CH₄, with the share of flammable gas components reaching about 45 vol%. The solid residues appear in the form of fine powder with visible metal inclusions of different sizes. All particles in the powder freed from the visible metal inclusions possess a size less than 300–400 μm, including a large fraction of sizes less than 100 μm. The powder contains Sn, Pb, Cu, Ni, Fe, In, Cd, Zn, Ca, Si, Al, Ti, Ni, and Cl. Among these substances, Sn (10–20 wt%), Pb (5–10 wt%), and Cu (up to 1.5 wt%) are detected in the maximum amounts. In the powder submitted for analysis, precious elements Ag, Au, and Pt are not detected. Some solid mass (about 20 wt% of the processed PCBs) is removed from the flow reactor with the escaping gas and is partly (about 10 wt%) trapped by the cyclones in the exhaust cleaning system. Metal inclusions of all visible sizes accumulate only in the flow reactor and are not detected in powder samples extracted from the cyclones. The gasification degree of the solid residues extracted from the cyclones ranges from 76 to 91 wt%, i.e., they are gasified only partly. This problem will be eliminated in future work. Full article