Life cycle GHG emissions assessment of vanadium recovery from bitumen-derived petcoke fly ash.

Petcoke generated during bitumen upgrading is a potential source of vanadium for the global market. Recovering vanadium from the fly ash originating from the combustion of petcoke appears to be a suitable route for commercial implementation, given its high extraction rate. Although the technical feasibility of the recovery process has been proven, the environmental impact should be addressed. Information on the greenhouse (GHG) emissions from the process is scarce in the public domain. Therefore, a framework was developed for assessment of life cycle GHG emissions for extraction of vanadium from petcoke-based fly ash. This framework was used to perform a life cycle GHG emissions assessment of a water leaching and salt roasting process to extract vanadium from fly ash. For the upstream GHG emissions, we collected direct emissions data and energy consumption from the literature, and, for the process emissions, we developed a model to estimate energy and material balances based on process conditions. The emission factors for electricity production, fuel combustion, production of consumables, and gas treatment were used to obtain the life cycle GHG emissions. The results show that the life cycle GHG emission of vanadium recovery are 26.6-3.9+0.9 kg CO2eq/kg V2O5; 66% of these are direct GHG emissions. The process GHG emissions from fly ash decarbonization contribute the most to the life cycle GHG emissions. The air-to-fuel ratio for roasting and the GHG emission factors for petcoke combustion and the gas treatment operation are the inputs that most effect the model output. Compared with the production of V2O5 from vanadium titano-magnetite ore and bitumen upgrading spent catalyst, the petcoke fly ash pathway generates about twice the life cycle GHG emissions. This study's results can help determine areas of improvement in the upstream operations and the recovery process to reduce the life cycle GHG emissions to levels that can compete with primary and alternative routes to produce vanadium pentoxide. The results of this study can help in decision-making associated with vanadium extract from fly ash produced from combustion of petcoke.

Long-term exposure to PM2.5 species and all-cause mortality among Medicare patients using mixtures analyses.

BACKGROUND: The relationship between long-term exposure to PM2.5 and mortality is well-established; however, the role of individual species is less understood. OBJECTIVES: In this study, we assess the overall effect of long-term exposure to PM2.5 as a mixture of species and identify the most harmful of those species while controlling for the others. METHODS: We looked at changes in mortality among Medicare participants 65 years of age or older from 2000 to 2018 in response to changes in annual levels of 15 PM2.5 components, namely: organic carbon, elemental carbon, nickel, lead, zinc, sulfate, potassium, vanadium, nitrate, silicon, copper, iron, ammonium, calcium, and bromine. Data on exposure were derived from high-resolution, spatio-temporal models which were then aggregated to ZIP code. We used the rate of deaths in each ZIP code per year as the outcome of interest. Covariates included demographic, temperature, socioeconomic, and access-to-care variables. We used a mixtures approach, a weighted quantile sum, to analyze the joint effects of PM2.5 species on mortality. We further looked at the effects of the components when PM2.5 mass levels were at concentrations below 8 µg/m3, and effect modification by sex, race, Medicaid status, and Census division. RESULTS: We found that for each decile increase in the levels of the PM2.5 mixture, the rate of all-cause mortality increased by 1.4% (95% CI: 1.3%-1.4%), the rate of cardiovascular mortality increased by 2.1% (95% CI: 2.0%-2.2%), and the rate of respiratory mortality increased by 1.7% (95% CI: 1.5%-1.9%). These effects estimates remained significant and slightly higher when we restricted to lower concentrations. The highest weights for harmful effects were due to organic carbon, nickel, zinc, sulfate, and vanadium. CONCLUSIONS: Long-term exposure to PM2.5 species, as a mixture, increased the risk of all-cause, cardiovascular, and respiratory mortality.

Valorization of fly ash by nickel ferrite and vanadium oxide recovery through pyro-hydrometallurgical processes: Technical and environmental assessment.

The fly ash (FA) from the combustion of heavy oil in power stations is characterized by fine particles containing toxic metals. The sample utilized in this study was gathered from the dust precipitators of seven heavy-oil-consuming Iranian power plants. Substantial quantities of heavy metals, particularly vanadium, iron, and nickel, have been detected in the sample, indicating both its potential utility and hazard to the soil and groundwater. The harmful consequences of FA disposal on the environment have led to the adoption of recycling as a treatment approach in this study. The valorization of FA was investigated by producing nickel ferrite (NiFe2O4) and vanadium pentoxide (V2O5) through a novel approach using a combination of pyro-hydrometallurgical processes, which resulted in proposing a recycling closed-loop flowsheet. Roasting was first practiced to form NiFe2O4 by reacting the nickel and iron content of the FA. The NiFe2O4 showed a low dissolution against inorganic acids (H2SO4, HCl, and HNO3). The vanadium content of the FA showed a remarkable recovery in H2SO4 (91%) and HCl (95.6%), while the dissolution of Ni was limited to 16.85% and 17.5%, respectively. The produced NiFe2O4 acted well in response to the magnetic field, and its purity was further increased to 95-96% through a two-stage process consisting of grinding and magnetic separation. The nano-sized spherical NiFe2O4 with saturation magnetization of 34.66 and 30.82 emu. g-1 was obtained from H2SO4 and HCl residues, respectively. The dissolved vanadium was recovered as V2O5 via oxidation-precipitation in sulfate media and oxidation-ammonium precipitation in chloride solution. The purity of V2O5 in sulfate and chloride media was 93% and 98.5%, respectively. Finally, a life cycle assessment (LCA) study was performed on the suggested methods to track the ecological effects of extracting V and Ni from oil combustion FA. According to the performed LCA, H2SO4 was determined as the proper leaching reagent considering the environmental and technical aspects.

Carbon capture technology exploitation for vanadium tailings and assessment of CO2 sequestration potential.

In recent years, the global warming trend is still increasing due to CO2 emissions from various sources, such as electricity, heat production, industry, and transportation. In the vanadium industry, the vanadium bearing shale is of low grade, and the extraction of the required elemental vanadium produces large quantities of vanadium tailings (VTs). Both the roasting pretreatment of vanadium shale during vanadium extraction and the high-temperature calcination process for the preparation of vanadium products generate large amounts of CO2 gas. Therefore, it is particularly important to find an effective and environmentally friendly method for the treatment of vanadium tailings and CO2 generated by the vanadium industry. In this study, a potential method for the indirect carbonation of low calcium VTs under atmospheric pressure conditions was investigated. The carbonation reaction was investigated for different ammonia addition factors and different introduced CO2 concentrations and temperatures. The carbonation experiments showed that under the conditions of coefficient of ammonia addition of 1.4, reaction time of 60 min and reaction temperature of 60 °C, the utilization rate of calcium in VTs reached 97.9% and the CO2 uptake of VTs at 0.073 g-CO2/g, indicating that the carbonation of vanadium with low-calcium VTs was effective. The carbonation product was analyzed and measured using TG, XRD, and SEM-EDS, and it was discovered to be CaCO3, confirming the feasibility of carbonation reaction with vanadium tailings. Furthermore, the characterization of the carbonation product confirmed the mechanism and safety of the carbonation reaction, laying the groundwork for future applications.

Activation of persulfate by vanadium oxide modified carbon nanotube for 17ß-estradiol degradation in soil: Mechanism, application and ecotoxicity assessment.

Steroid hormones in the environment have attracted public attention because of their high endocrine-disrupting activity even at rather low exposure level. Excessive hormones in the soil from the pollutant discharge of intensive farming would pose a potential threat to the ecology and the human health. Vanadium oxide modified carbon nanotube (VOX-CNT) was synthesized and applied as persulfate (PDS) activator to reduce17ß-estrogen (17ß-E2) in soil. 86.06 % 17ß-E2 could be degraded within 12 h. Process of materials exchange during oxidation was interfered by soil, resulting in insufficient degradation of 17ß-E2, but the active species involved in 17ß-E2 degradation would also be enriched by it. 17ß-E2 was adsorbed on the VOX-CNT surface and directly degraded mainly by the active species generated on the catalyst surface, and •OH dominated the degradation of 17ß-E2 in VOX-CNT/PDS system. CO, defective sites and vanadium oxides on the surface of VOX-CNT contributed to the generation of activate species. Oxidizer dosage, catalyst dosage, water-soil ratio and soil properties would affect the degradation of 17ß-E2. The ecotoxicological impact on soil caused by VOX-CNT/PDS was acceptable, and would be weakened with time. Additionally, a rapid decrease in the concentration of 17ß-E2 and the promotion of maize growth were observed with VOX-CNT/PDS in situ pilot-scale remediation. Those results reveal that VOX-CNT/PDS is a potential technology to remove excessive steroid hormone from soil around large-scale livestock and poultry farms.

Risk assessment and microbial community structure in agricultural soils contaminated by vanadium from stone coal mining.

High health risks of vanadium (V) released by the mining of vanadium titanomagnetite (VTM) have been widely recognized, but little is known about the risks and microbial community responses of V pollution as a consequence of the stone coal mining (SCM), another important resource for V mining. In this study, the topsoils and the profile soils were collected from the agricultural soils around a typical SCM in Hunan Province, China, with the investigation of ecological, health risks and microbial community structures. The results showed that ∼97.6% of sampling sites had levels of total V exceeding the Chinese National standard (i.e., 130 mg/kg), and up to 41.1% of V speciation in the topsoils was pentavalent vanadium (V(V)). Meanwhile, the proportions of HQ > 1 and 0.6-1 in the topsoils were ∼8.3% and ∼31.0% respectively, indicating that V might pose a non-carcinogenic risk to children. In addition, the microbial community varied between the topsoils and the profile soils. Both sulfur-oxidizing bacteria (e.g. Thiobacillus, MND1, Ignavibacterium) and sulfate-reducing bacteria (e.g. Desulfatiglans, GOUTB8, GOUTA6) might have been involved in V(V) reductive detoxification. This study helps better understand the pollution and associated risks of V in the soils of SCM and provides a potential strategy for bioremediation of the V-contaminated environment.

Development of peptide impregnated V/Fe bimetal Prussian blue analogue as Robust nanozyme for colorimetric fish freshness assessment.

Colorimetric sensing is a low-cost and visual method for food freshness monitoring. We prepared a Vanadium-Iron Prussian blue analogue (V1/5Fe(CN)6 PBA) impregnated with insulin (INS), as a peroxidase-like mimetic probe toward 3,3'5,5'-tetramethylbenzidine (TMB) oxidation and colorimetric monitoring of fish freshness. A specific chemical reaction between putrescine as spoilage marker and the Vanadium-Iron V1/5Fe(CN)6PBA impregnated with insulin (V1/5Fe(CN)6PBA/INS) induces a decreasing peroxidase-like activity of the V1/5Fe(CN)6PBA/INS, generating lower amounts of oxidized products of TMB. The proposed bio-strategy achieved highly sensitive responses in the range of 30 nM to 12 µM toward putrescine with a detection limit of 9.0 nM and outstanding stability, reproducibility, and selectivity. The freshness of five different types of fish samples determined and produces a noticeable color change consistent with the stale fish around the 10 µM, which can warn the oldness of the fish. This new strategy of integration between peptide and multi-metal PBA with intensified enzyme-like mimetics activity may be highly meaningful for thoroughly monitoring the amount of fish freshness.

Novel metallomic profiling and non-carcinogenic risk assessment of botanical ingredients for use in herbal, phytopharmaceutical and dietary products using HR-ICP-SFMS.

Knowledge of element concentrations in botanical extracts is relevant to assure consumer protection given the increased interest in plant-based ingredients. This study demonstrates successful multi-element investigations in order to address the lack of comprehensive profiling data for botanical extracts, while reporting for the first time the metallomic profile(s) of arnica, bush vetch, sweet cicely, yellow rattle, bogbean, rock-tea and tufted catchfly. Key element compositions were quantified using a validated HR-ICP-SFMS method (µg kg-1) and were found highly variable between the different plants: Lithium (18-3964); Beryllium (3-121); Molybdenum (75-4505); Cadmium (5-325); Tin (6-165); Barium (747-4646); Platinum (2-33); Mercury (5-30); Thallium (3-91); Lead (12-4248); Bismuth (2-30); Titanium (131-5827); Vanadium (15-1758); Chromium (100-4534); Cobalt (21-652); Nickel (230-6060) and Copper (1910-6340). Compendial permissible limits were not exceeded. Overall, no evidence of a health risk to consumers could be determined from consumption of the investigated plants at reasonable intake rates. Mathematical risk modelling (EDI, CDI, HQ, HI) estimated levels above safe oral thresholds only for Cd (16%) and Pb (8%) from higher intakes of the respective plant-derived material. Following high consumption of certain plants, 42% of the samples were categorised as potentially unsafe due to cumulative exposure to Cu, Cd, Hg and Pb. PCA suggested a potential influence of post-harvest processing on Cr, Ti and V levels in commercially-acquired plant material compared to wild-collected and farm-grown plants. Moreover, a strong correlation was observed between Pb-Bi, Be-V, Bi-Sn, and Tl-Mo occurrence. This study may support future research by providing both robust methodology and accompanying reference profile(s) suitable for the quality evaluation of essential elements and/or metal contaminants in botanical ingredients.

An integrated biomarker assessment of biochemical responses in a freshwater fish species after vanadium pentoxide (V2O5) exposure.

Vanadium (V) is a toxicant becoming increasingly concentrated in freshwater with the potential to affect aquatic organisms. Vanadium pentoxide (V2O5), accumulated in fish, can act as an oxidizing agent and cause oxidative damage. To determine the effects of V2O5 on exposed adult Oreochromis mossambicus, acute exposure experiments were conducted. Bioaccumulation and biomarker analyses were performed on various excised tissues of the exposed fish. As expected, accumulated V concentrations in the gills increased as the exposure concentration increased. Gill tissue accumulated more vanadium than muscle tissue. Metallothionein content increased in the highest concentrations compared to the lower concentrations, therefore showing that metallothionein proteins were attempting to sequester V2O5 in the tissues. Superoxide dismutase (SOD) showed an excitation at lower concentrations and inhibition as the exposure concentrations increased, possibly due to ROS detoxification. Catalase activity decreased from the first exposure concentration to the last concentration; this could have been due to SOD compensation. Protein carbonyl concentration decreased as the concentrations of V2O5 increased, indicating an inhibition of protein oxidation. The IBRv2 comparison revealed the biochemical responses caused by V2O5 more effectively than traditional statistical analysis.

Metal exposure and breast cancer among Northern Mexican women: assessment of genetic susceptibility.

This study aims to assess breast cancer (BC) association with metals and whether polymorphisms in CYP1A1, CYP1B1, GSTM1 and GSTT1 act as confounders or as modifiers of those relationships. We performed a secondary analysis of 499 histologically confirmed BC cases and the same number of age-matched population controls. We measured urinary concentrations of 18 metals with mass spectrometry. We determined the genetic variants of interest by allelic discrimination and multiplex PCR. After adjusting for covariates, we found BC negatively associated with arsenic, barium, cobalt, copper, magnesium, molybdenum and vanadium concentrations and positively with those of caesium, manganese, tin and thallium. Most associations remained after stratifying by the genetic variants. We identified that polymorphisms in CYP1B1, CYP1A1 and GSTM1 genes interacted with some metals on BC: interaction p-values CYP1B1 G119T × antimony= 0.036, CYP1B1 G119T × cobalt <0.001, CYP1B1 G119T × tin= 0.032, CYP1A1 A4889G × aluminium= 0.018, CYP1A1 A4889G × arsenic= 0.031, CYP1A1 A4889G × nickel= 0.036, CYP1A1 A4889G × vanadium= 0.031 and GSTM1 deletion × barium= 0.035. Exposure to various individual metals, along with genetic characteristics may contribute to BC development. Further studies are warranted to confirm our results.

Spatial distribution and pollution assessment of heavy metals in sediments from the Brahmaputra River watershed in Bangladesh.

Spatial distribution and pollution assessment of selected heavy metals such as barium (Ba), chromium (Cr), nickel (Ni), lead (Pb), vanadium (V), arsenic (As), zinc (Zn), and copper (Cu) in sediments of the Brahmaputra River watershed in Bangladesh was investigated. The mean abundances (ppm) of heavy metals in sediment samples were in decreasing order Ba (375.60) > V (67.60) > Cr (54.10) > Zn (48.20) > Ni (22.28) > Pb (20.25) > Cu (7.59) > As (4.21). Concentrations of Pb and As in the sediments are enriched relative to the average upper continental crust composition, while Ba, V, Cr, Zn, Ni, and Cu decrease considerably. A higher concentration of Pb and Ni indicates that Brahmaputra River watershed samples receive a significant contribution from anthropogenic sources of heavy metals. Chromium displays marked positive correlation with V (r = 0.91, p = < 0.01), inferring a similar source materials input into the watershed. The geo-accumulation index (Igeo) values suggest that the sediments were uncontaminated to moderately contaminated by Ni, Zn, Pb, V, and Cr, whereas moderate to heavily contaminated by As and Cu. The contamination factor (CF) confirmed that sediments in the watershed were moderate to highly contaminated by As, Cu, and Cr. The pollution load index (PLI) values for most of the samples were over one (> 1), indicating an advanced decline in the watershed sediment quality. The overall results of a multivariate statistical analysis suggest that Ba, V, Cr, and Zn contents were all-natural sources, and Pb, Ni, As, and Cu were derived from both natural and anthropogenic sources.

The Content of Cobalt, Silver and Vanadium in Raw Cow's Milk in Croatia and Risk Assessment for Consumers.

Concentrations of selected trace elements Ag, Co and V in raw milk sampled from four geographical regions in Croatia were measured. Silver, Co and V were detected above the limit of detection within the range of 9.52%-30.8%, 1.6%-12.1% and 12.4%-30.8%. Silver concentrations were not detected in milk samples from the Croatian Littoral and Mountainous Croatia (CL-MC) region. Similar Ag content was found in Southern, Eastern and Central Croatia. The lowest mean of Co and V of 33.2 and 83.8 µg kg-1 were found in the CL-MC region while the highest of 49.8 and 136.9 µg kg-1 was found in Central Croatia. There were no statistically significant differences in Ag, Co and V contents between the four regions. The estimated daily dietary intakes (EDI) of total mean and total 95th percentile values of Ag, Co and V showed lower values in comparison with available EFSA health-based limits.

Development of economical and highly efficient electrolyte using vanadium pentoxide for vanadium redox flow battery.

Vanadium pentoxide can be an inexpensive replacement to vanadium sulfate in synthesizing vanadium redox flow battery (VRFB) electrolytes. In this study, VRFB electrolyte is synthesized from vanadium pentoxide using an indigenously developed process and setup. In order to have the same performance as that of vanadium sulfate, the supporting electrolyte environment constituted by H+ and sulfate ion is replicated based on the calculations from standard synthesis mechanisms. The calculations reveal that 4 M H2SO4 is required while preparing 1.5 M Vn+ electrolyte from V2O5 to replicate 1.5 M Vn+ in 2.5 M H2SO4 from VOSO4. The effect of variation of sulfuric acid concentration is explored using thermal stability testing, which shows stable V(V) electrolytes for more than 30 days for 4 M H2SO4 concentration. Furthermore, the electrochemical performance of developed electrolyte from vanadium pentoxide shows similar charge-discharge profile, yet 1/5 the cost as compared to vanadium sulfate.

Life cycle sustainability assessment of optimized biodiesel production from used rice bran oil employing waste derived-hydroxyapatite supported vanadium catalyst.

The present work encompasses the production of biodiesel from an inexpensive waste, viz., used rice bran oil (URBO) through concurrent esterification and transesterification reactions employing the prepared waste duck bone (WDB)-derived natural hydroxyapatite (NAHAp) supported vanadium impregnated solid catalyst (VNAHAp). The optimal VNAHAp catalyst possessed 92.23 m2/g surface area which was much superior to 61.46 m2/g of the V-catalyst (VCHAp) prepared using commercially available hydroxyapatite (CHAp). The optimal (Box-Behnken design) concurrent trans/esterification reaction conditions for biodiesel (FAME) production from URBO and methanol were 5 wt.% catalyst concentration, 8:1 methanol/URBO mole ratio, and 35 wt% NH4VO3 loaded VNAHAp (35VNAHAp) catalyst that resulted in 99.05% FAME yield deploying a low-energy infrared radiator assisted batch reactor (LIRABR) which ensured significantly high FAME yield at milder temperature (60°C) and in shorter reaction time (30 min) compared to a conventionally heated batch reactor. The product biodiesel and its blend with commercial diesel conformed to ASTM D7467-10 specifications. The life cycle assessment (LCA) of the entire process advocated superior sustainability of the biodiesel production using 35VNAHAp catalyst in the LIRABR compared to their conventional counterparts. Valorization of two potential wastes, viz., URBO and WDB, under milder process conditions involving LIRABR and 35VNAHAp resulted in lower environmental impacts, thus rendering a sustainable biodiesel production process towards a greener earth.

Assessment of Arsenic, Vanadium, Mercury, and Cadmium in Food and Drug Packaging.

Background: Food and drug packaging materials are an integral part of our everyday life.  Noxious elements can inadvertently be included in packaging materials in various stages of their production. Adulterants, adhesives, colorants and heavy metal interference are the common sources of contamination in food packaging materials. Heavy metal toxicity has far-reaching ill effects on living organisms. The present study aimed at qualitatively and quantitatively analysing heavy metal content of various materials that are used for food and drug packaging in India. Methods: The qualitative detection was done by rapid assay and heavy metals were quantified with the help of inductively coupled plasma-optical emission spectrometry (ICP-OES). A total of thirteen types of food and drug packaging materials were procured from local market and analysed for four heavy metals viz. arsenic (As), vanadium (V), mercury (Hg) and cadmium (Cd). The concentration of each heavy metal in the samples was compared with the permissible values published by the European Council. Results: Heavy metals were qualitatively detected in ten out of thirteen samples. Among the ten samples mercury and arsenic were detected the most followed by cadmium and vanadium. Quantitative estimation by ICP-OES showed presence of vanadium and cadmium in ten samples and arsenic and mercury in all the thirteen samples above the permissible range. Conclusions: The notable elevation in mercury concentration, followed by cadmium, arsenic and vanadium registering the least, presents a potential health hazard to consumers and compromises the food quality.

Bioleaching of vanadium by Acidithiobacillus ferrooxidans from vanadium-bearing resources: Performance and mechanisms.

Bioleaching is promising to meet the demand of strategic vanadium both economically and environmentally. Whereas the combination of bioleaching with traditional techniques is of great interest, little is known on bioleaching of vanadium from abundant vanadium-bearing resources utilized/produced in existing processes. This study investigated the bioleaching of vanadium from vanadium-titanium magnetite, steel slag, and clinker, which are common raw mineral and intermediates used in conventional vanadium extraction process. Clinker had greater leachability by Acidithiobacillus ferrooxidans, compared to vanadium-titanium magnetite and steel slag. Pulp density, inoculum volume, initial pH and initial Fe2+ concentration had influencing effects on this bioleaching process. Under optimal condition with 3% pulp density, 10% inoculum volume, initial pH at 1.8, and 3 g/L initial Fe2+ concentration, the bioleaching of clinker achieved the maximum vanadium leaching efficiency of 59.0%. Both X-ray fluorescence and energy dispersive spectroscopy analysis confirmed the reduction of vanadium content in the solid residues after leaching. The results of Community Bureau of Reference sequential extraction suggested that vanadium in acid-soluble and oxidizable phase was more easily leachable. This study is helpful to develop sustainable and practical techniques for vanadium extraction from abundant raw materials and step forward in combining bioleaching with traditional process.

A global systematic review, meta-analysis, and risk assessment of the concentration of vanadium in drinking water resources.

The presence of toxic metals such as vanadium in water resources has attracted considerable attention as a new concern in international health. Systematic review and meta-analysis were performed to assess the concentration of vanadium in water resources along with the relevant ecological risk assessment. Databases of Scopus, PubMed, and Embase were investigated to retrieve the related articles from January 01, 1974 to December 25, 2019. Twenty-eight articles containing 152 samples from 24 countries were included. Furthermore, the meta-analysis was conducted by the approach of z-score to estimate differences in the effect size. In addition, the mean of concentrations of vanadium was applied to calculate the risk assessment only to the water surface and choose the maximum environmental concentration (MEC) for demonstrate a worst-case scenario. Here, the risk assessment approach was used to show that the MEC of vanadium confirm the risk it for aquatic ecosystems, being fish (e.g., Danio rerio) our model organism due to their sensibility. According to findings, the MEC of vanadium in surface water varied from 0.010 µg L-1 (USA) and 68 µg L-1 (China), with an overall mean of 6.21 ± 13.3 µg L-1 (mean ± standard deviation). The ecological risk assessment demonstrated that people living in some countries such as China and Japan were at an adverse ecological risk of vanadium in the water resources. Hence, essential control plans besides adequate removal techniques must be implemented for significant deracination of heavy metals like vanadium.

Punching above its weight: life cycle energy accounting and environmental assessment of vanadium microalloying in reinforcement bar steel.

Steel-reinforced concrete is ubiquitously used in construction across the world. The United Nations estimates that the worldwide energy consumption of buildings accounts for 30-40% of global energy production, underlining the importance of the judicious selection of construction materials. Much effort has focused on the use of high-strength low-alloy steels in reinforcement bars whose economy of materials use is predicated upon improved yield strengths in comparison to low-carbon steels. While microalloying is known to allow for reduced steel consumption, a sustainability analysis in terms of embodied energy and CO2 has not thus far been performed. Here we calculate the impact of supplanting lower grade reinforcement bars with higher strength vanadium microalloyed steels on embodied energy and carbon footprint. We find that the increased strength of vanadium microalloyed steel translates into substantial material savings over mild steel, thereby reducing the total global fossil carbon footprint by as much as 0.385%. A more granular analysis pegs savings for China and the European Union at 1.01 and 0.19%, respectively, of their respective emissions. Our cradle-to-gate analysis provides an accounting of the role of microalloying in reducing the carbon footprint of the steel and construction industries and highlights the underappreciated role of alloying elements.

Human health risk of vanadium in farmland soils near various vanadium ore mining areas and bioremediation assessment.

Various kinds of vanadium (V) ore mining areas produced serious contamination have been widely recognized, while less relevant research was about the associated health risk and V distribution level for farmland soils around. This study assessed the contamination characteristics and associated human health risk of V in the surface farmland soils near various V ore mining areas. The bioremediation of V contamination by indigenous microbes from them was also evaluated. The farmland soils near stone coal area (Hunan province, China) showed the highest mean concentration of V (543.91 mg/kg), posing high non-carcinogenic risks, with high hazard quotient (HQ) value of 1.29 for children. While, V values of sampled soils near V titanomagnetite, petroleum associated minerals and uvanite areas were lower than that near stone coal area, also with lower HQ values (<1.00). Within 60 h, the removal efficiency of V(V) reached 98.4% with farmland soils near uvanite area, suggesting feasibility of V bioremediation via indigenous microbes. Bacterial communities after long-term cultivation (240 d) with V(V) were dominated by native microbes able to tolerate or reduce the toxicity of V(V), such as Ruminococcaceae_incertae_sedis, Trichococcus and Comamonas. This work is helpful for calling attention to V pollution of farmland near various V ore mining areas and formulating effective strategies for V(V) contamination bioremediation.

Recovery of chromium, copper and vanadium combined with electricity generation in two-chambered microbial fuel cells.

Microbial fuel cells (MFCs) offer a promising solution towards recovery and treatment of heavy metal pollutants. In this study, two-chambered MFCs were employed for recovery of chromium, copper and vanadium (Cr (VI), Cu (II) and V (V)). One g/L concentrations of K2Cr2O7, CuCl2 and NaVO3 served as catholytes, while a mixed culture was used as anolyte. Cr (VI), Cu (II) and V (V) were reduced biologically into less toxic forms of Cr (III), Cu and V (IV) respectively. Power density and cathodic efficiency were calculated for each of the catholytes. Cr (VI) gave the maximum power density and cathodic efficiency due to its high redox potential. Current produced depended on the concentration of the catholyte. Over a period of time, biological reduction of catholytes lead to decrease in the metal concentrations, which demonstrated the application of MFC technology towards heavy metal treatment and recovery in a reasonably cost-effective manner.