Metals Zn Research Articles

Anthropogenic activities affect the diverse autotrophic communities of coastal sediments

Coastal sediments are a critical domain for carbon sequestration and are profoundly impacted by human activities. Therefore, it is essential to understand the structure and components of benthic autotrophs that play a crucial role in carbon sequestration processes, as well as the influence of anthropogenic activities on their communities. This study utilized an urban estuary, an industrial sea bay, a maricultural sea region, and two mangrove coastlines within the coastal areas of Guangdong Province, China. The micro-benthos in these environments, including prokaryotes and eukaryotes, were identified through high-throughput sequencing of 16S rRNA and 18S rRNA genes. The findings show that the autotrophic composition was altered by the interactions of anthropogenic heavy metals (Cd and Zn) and micro-eukaryotes (protazoa, metazoa, and parasitic organisms). Industrial pollution reduced the abundance of both prokaryotic and eukaryotic autotrophs. Mangroves induced a substantial transformation in the sediment eukaryotic and prokaryotic composition, increasing the proportion of autotrophs, notably sulfur-oxidizing and iron-oxidizing bacteria and microalgae. This alteration suggests an increase in specific sulfur and iron cycling with simultaneous carbon sequestration within mangrove sediments. These results indicate that anthropogenic activities affect sediment carbon sequestration by altering autotrophic assemblages along coastlines, thereby inducing consequential shifts in overall elemental cycling processes.

Comprehensive Assessment of Heavy Metal Contamination in Soil-Plant Systems and Health Risks from Wastewater-Irrigated Vegetables

A research study examined the origins, human health impacts, and risks associated with pollutants in vegetables grown in soil irrigated with wastewater. The study analyzed 164 samples from water sources, irrigated soil, and harvested vegetables for eight heavy metals (Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn) using atomic absorption spectrophotometry. The focus was on the potential health effects of consuming heavy metal-contaminated vegetables grown in wastewater-irrigated soil. The findings revealed significant accumulation of heavy metals in soil and plants from Mianwali, Pakistan, posing potential health risks to consumers. When compared to vegetables produced with freshwater irrigation, the concentration levels of heavy metals in the soil irrigated with untreated wastewater were significantly greater (P≤0.001) and above the recommended limits set by the World Health Organization (WHO). The results showed that heavy metals in the soil had significantly increased, and crops had subsequently absorbed these metals. Produce raised in soil watered with wastewater showed higher levels of heavy metals than the US Environmental Protection Agency (EPA) and the WHO recommended. Among the veggies, lead (Pb) and cadmium (Cd) were found to have higher Hazardous Quotient Indices (HRIs) than one. This indicates that both adults and children may have been exposed to dangerous levels of these metals. Additionally, for Brassica oleracea, Raphanus sativus, and Spinacia oleracea, nickel (Ni) surpassed HRIs larger than 1, indicating a significant health risk connected to these veggies' ingestion.

Understanding and Mastering Multiphysical Fields Toward Dendrite‐Free Aqueous Zinc Batteries

AbstractAqueous zinc batteries (AZBs) have emerged as promising candidates for next‐generation grid‐scale energy storage due to their excellent safety, environmental friendliness, and abundance of Zn metal. However, undesired dendrite growth on Zn anodes, resulting from uneven Zn plating/stripping, leads to poor durability and low Coulombic efficiency, posing significant challenges for the practical application of AZBs. Multiple physical fields, the intrinsic driving force governing the distribution of electrons and ions, significantly impact Zn deposition behavior. The underlying mechanisms and regulation strategies related to this phenomenon has not been fully reviewed. This comprehensive review focuses on revealing the key physical fields influencing Zn deposition (including ionic flux, electric field, stress field, and temperature field) and summarizes the most effective control methods. Each approach is thoroughly scrutinized, highlighting its operational mechanisms, benefits, and limitations. Furthermore, the challenges and potential pathways for developing durable Zn anodes are outlined. Through in‐depth analysis of the influences of multiphysical fields on Zn deposition behavior, this review sets the foundation for enhancing the performance of Zn anodes, thereby supporting the advancement of Zn batteries commercialization.

Comparative analysis of the physicochemical properties and trace metal content of palm oil, from selected markets in Jos south and Jos north LGA, Plateau state, Nigeria

The quality of palm oil samples collected from three different markets in Jos South and Jos North Local Government Area of Plateau State were analyzed and evaluated using standard analytical laboratory procedures. The relative ranges of the physicochemical values obtained were as follows; Moisture Content (MC): 0.56 - 1.89, Iodine value (IV); 51.88 - 55.57 g I2/100g, Peroxide Value (PV): 0.98 - 4.16 mEq02/kg, Saponification Values (SV): 198.46 - 201.54 mgKOH/g, Acid Value (AV): 9.93 - 57.65, and Refractive Index (RI), 1.4576 - 1.4580. The moisture content, iodin value, pH values and acid values were found to exceed the Standard Organization of Nigeria (SON) permissible limits of moisture content (0.29 mgKOH/g), iodine value (45 - 53 mg I2/100g), pH (5 - 7 mg/L), and acid value (0.7 max mg/L) for edible oils respectively while the refractive index, saponification values, peroxide values falls within the SON allowable limits of refractive index (1.4612-1.4707 mg/L), saponification value (195-205 mgKOH/g) and peroxide value (10 mEq02/kg) respectively . The amounts of trace metals (Cu, Zn, Fe, Pb and Cd) determined in the palm oil using the atomic absorption spectrophotometer ranged from Cu(0.34 - 0.52 mg/l), Zn(1.58 - 2.33 mg/l), Fe(19.18 - 26.74 mg/l), Pb(2.87 - 4.06 mg/l) and Cd(1.58 - 2.24 mg/l). However, the levels of Zn, Fe, Pb and Cd exceeded the WHO/FAO recommended values of (1.50, 1.00, 0.05 and 0.02 mg/L) respectively while only Cu concentration was below the WHO/FAO limits of 2.00 mg/L for trace metals in edible palm oil. Consequently, the results of this study shows that the palm oil consumed from these selected markets does not meet the standard quality specification for edible palm oils and hence can post significant health threat to consumers. Therefore, food regulatory agencies should strengthen their surveillance to promote food and health safety of the populace.

U–Pb geochronology of carbonate-hosted Pb–Zn ores reveals plate-tectonic evolution of eastern Asia during the early Paleozoic

The Mississippi Valley–type (MVT) deposits reached their maximum abundance during the final assembly of Pangea. The intense orogenic activity during this assembly in relatively low latitudes created abundant opportunities for the migration of sedimentary brines into the interior carbonate platforms landward of the orogenic belts, leading to the formation of MVT deposits. Thus, dating the MVT deposits can potentially aid in the reconstruction of the plate tectonic evolution during the assembly of Pangea. The Yangtze Craton hosts significant carbonate-hosted Zn–Pb deposits (> 60 Mt Pb + Zn metals), accounting for 30% of China’s Zn–Pb resources. However, determining the timing of zinc and lead mineralization in these reservoirs is challenging. This study employs LA-ICP-MS U–Pb geochronology on calcites to date Zn–Pb deposits hosted in Lower Cambrian limestone in the Huayuan orefield. Three generations of calcite formation were dated: the first recorded the pre-ore deposition of Lower Cambrian limestone at 517 ± 10 Ma, the second marked a hydrothermal event linked to stratiform sphalerite ore formation at 501.4 ± 8.4 Ma, and the third was associated with discordant breccia-hosted Zn–Pb mineralization at 397.5 ± 9.6 Ma. Our results indicate that Paleozoic carbonate-hosted Pb–Zn mineralization in the Yangtze Craton is linked to (1) the final assembly of Gondwana in the late Cambrian-early Ordovician (520–480 Ma); and (2) the intracontinental orogeny response to Jiangnan Uplift (420–400 Ma). This study highlights the temporal relationship between low temperature carbonate-hosted mineralization and orogenic events that are consistent with classic MVT models worldwide. It also contributes geochronological data for the reconstruction of plate-tectonic evolution during Pangea assembly. Furthermore, it demonstrates the potential of in situ U–Pb calcite geochronology to date ore deposits lacking syn-ore minerals suitable for traditional dating methods.

The Comprehensive Effects of Biochar Amendments on Soil Organic Carbon Accumulation, Soil Acidification Amelioration and Heavy Metal Availability in the Soil–Rice System

In recent years, biochar (BC) and biochar-based soil amendments (CSAs) have been widely used in agriculture and the environment. In the present study, a two-rice-season field study was conducted to explore the comprehensive effects of applying BC (1%) and CSA (0.5% and 1%) on soil organic carbon accumulation, soil acidification amelioration and heavy metal availability in a soil–rice system. The results show that soil pH was increased by 0.5–1.7 units and 0.3–1.0 units, respectively, in the early rice season and late rice season treated by the amendments compared with CK. Soil organic contents were increased by 18–30% in the early rice season and by 15–25% in the late rice season in the amended treatments. In addition, soil available phosphorus contents were largely increased as a result of BC and CSA addition. Soil CaCl2 extractable heavy metals (Cd, Ni, Cu and Zn) were simultaneously decreased by BC or CSA amendments. In addition, Cd contents in early rice grain and late rice grain were significantly reduced by 25–48% and 52–83% in amended treatments, while Zn contents were generally not affected. The uptake of Cu and Ni was also decreased by BC and CSA. This study demonstrates that biochar application alone or combinates with inorganic amendments (limestone, sepiolite and potassium dihydrogen phosphate) can significantly improve soil properties and nutrient content and decrease the heavy metal (especially for Cd and Ni) uptake and accumulation from soil to rice grain, where the combination application is more effective.

A Dynamically Ion‐Sieved Electrolyte towards Ultralong‐Lifespan Zn‐Ion Batteries

AbstractThe practical deployment of Zn‐ion batteries faces challenges such as dendrite growth, side reactions and cathode dissolution in traditional electrolytes. Here, we develop a highly conductive and dynamically ion‐sieved electrolyte to simultaneously enhance the Zn metal reversibility and suppress the cathode dissolution. The dynamic ion screen at the electrode/electrolyte interface is achieved by numerous pyrane rings with a radius of 3.69 Å, which can selectively facilitate the plating/stripping and insertion/extraction process of [Zn(H2O)6]2+ and Zn2+ on the anode and cathode surfaces. As a proof of concept, Zn//Zn symmetric cells deliver exceptional cyclic stability for over 6,800 h and ultrahigh cumulative plated capacity of 1.95 Ah cm−2. Zn//Na2Mn3O7 cells exhibit satisfactory cycling performance with capacity retention of 82.7 % after 4,000 cycles, and the assembled pouch cells achieve excellent stability and durability. This work provides valuable insights into the development of electrolytes aimed at enhancing the interface stability of aqueous batteries.

Metal contamination in mangrove tissues, seeds, and associated sediments from the Vattanam mangrove forest of Palk Bay, southeastern India: An ecological risk assessment

In the present work, the concentrations of toxic heavy metals in mangrove sediments, mangrove leaves, and seeds collected from five stations in the Vattanam mangrove of Palk Bay, southeastern India, as well as the effects of the monsoon season on toxic heavy metals concentrations were determined. The concentrations were 17.5 μg/g for zinc (Zn), 9.11 μg/g for copper (Cu), and 6.03 μg/g for lead (Pb) in sediments; 10.71 μg/g (Zn) and 8.94 μg/g (Cu) in mangrove leaves; and 26.24 μg/g (Zn) and 17.01 μg/g (Cu) in mangrove seeds. At all sampling stations, the Cd concentration was below the limit of detection. These mangroves seem to have adapted successfully to their environment given their selective intake of only essential metals (Cu and Zn) and the restricted movement of non-essential metals (Cd and Pb). The concentrations of metals were below the maximum residual limits regulated by national and international standard limits.

Effects of filling substrates on remediation performance and sulfur transformation of sulfate reducing packed-bed bioreactors treating acid mine drainage

The filling substrate is one of key factors influencing effectiveness of sulfate reducing packed-bed bioreactor (SRPB) treating acid mine drainage (AMD). The effects of four substrates (i.e. quartz sand, steel residue, biochar, and peanut shell) on remediation performance and sulfur transformation of SRPB treating AMD was studied. The results showed that steel residue and biochar improved sulfate reduction efficiency (61% and 49%) compared to quartz sand (32%), whereas peanut shell inhibited sulfate reduction efficiency (19%), attributed to its decomposition process leading to a severe accumulation of acetic acid. More amounts of sulfides generated in steel residue bioreactor were converted into acid volatile sulfide and elemental sulfur, resulting in a significant decrease in dissolved sulfide in the effluent. Metals (Fe, Al, Zn, Cd and Cr) except for Mn were effectively immobilized in the bioreactors, particularly for Al and Cd. Sulfate reducing bacteria and sulfide oxidizing bacteria lived symbiotically in all bioreactors which exhibited similar heterogeneity in microbial distribution and function, i.e. bacterial sulfate reduction mainly occurring in bottom-middle layers and photoautotrophic sulfide oxidation in upper layer close to outlet. The microbial response mechanism to various substrate environments was revealed through co-occurrence networks analysis. This study suggests that attention should be paid to the inhibitory effect of acetic acid accumulation on sulfate reduction when using sole lignocellulosic waste (peanut shell), and steel residue and biochar could be utilized as filling substances to promote sulfate reduction.

Drill cuttings from oil exploration improve properties of substrate and growth of Ipê-branco ( Tabebuia roseoalba ) seedlings

ABSTRACT More information is needed on the potential of using drill cuttings (crushed rocks) from the oil industry in agriculture and forestry. An experiment in forest nursery was carried out to evaluate the influence of substrates formulated from onshore gravel on characteristics of Ipê-branco (Tabebuia roseoalba) seedlings (i.e., growth, quality, and nutrition). We used five gravimetric proportions of gravel from drill cuttings mixed with Pinus-bark - commercial substrate (Mecplant® Florestal 3): control with only commercial substrate and zero gravel (G0), 2.5 % gravel (G2.5), 5 % gravel (G5), 7.5 % gravel (G7.5), and 10 % gravel (G10). In general, high proportion of drill cuttings increases density and decrease current moisture and total porosity of the formulated substrates. The drill cuttings proportions G2.5, G5 and G7.5 significantly contributed to the available water and readily available water in these substrates, with percentage values ranging 23 – 30 % higher than the G10 substrate. Increasing the gravel proportion generally resulted in increased pH levels, P, Na, K and metals (Cu, Fe, Ni, Mn, Cd, Zn, Cr and Pb), except for Ca and Mg nutrients that decreased. Heavy metal contents in all substrates did not exceed the permissible values in legal standards. The G2.5 and G5 substrates increased by 20 % approximately the stem diameter and height of seedlings, and G2.5 proportion also affected the root dry mass and Dickson quality index, with values two times higher than G0 substrate. Multivariate analysis proved suitable as a complementary approach to evaluate the seedling quality. Drilling cuttings addition, in general, increased the accumulation of nutrients and heavy metals of the Ipê-branco seedlings, and G2.5 and G5 substrates provided the greatest accumulation of the nutrients P, Ca, Pb and Zn in the shoot, while G2.5 proportion contributed with higher accumulation of N, Ca, Fe, Cr, Mn and Pb in the root. Adding drill cuttings as a conditioning component of the substrate at 2.5 and 5 % proportions is a viable alternative for using this residue to produce high-quality Tabebuia roseoalba seedling.

Band Engineering of Mn-P Alloy Enables HER-suppressed Aqueous Manganese Ion Batteries.

Aqueous manganese ion batteries hold potential for stationary storage applications owing to their merits in cost, energy density, and environmental sustainability. However, the formidable challenge is the instability of metallic manganese (Mn) anodes in aqueous electrolytes due to severe hydrogen evolution reaction (HER), which is more serious than the commonly studied Zn metal anodes. Moreover, the mechanism of HER side reactions has remained unclear. Herein, we design a series of Mn-P alloying anodes by precisely regulating their energy band structures to mitigate the HER issue. It is found that the serious HER primarily originates from the spontaneous Mn-H2O reaction driven by the excessively high HOMO energy level of Mn, rather than electrocatalytic water splitting. Owing to a reduced HOMO energy level and enhanced electron escape work function, the MnP anode achieves an evidently enhanced cycle durability (over 1000 hours at a high current density of 5 mA cm-2). The MnP||AgVO full cell with an N/P ratio of 4 exhibits better rate capability and extended cycle life (7000 cycles) with minimal capacity degradation than the cell using metallic Mn anode (less than 100 cycles). This study provides a practical approach for developing highly durable aqueous Mn ion batteries.

Band Engineering of Mn‐P Alloy Enables HER‐suppressed Aqueous Manganese Ion Batteries

Aqueous manganese ion batteries hold potential for stationary storage applications owing to their merits in cost, energy density, and environmental sustainability. However, the formidable challenge is the instability of metallic manganese (Mn) anodes in aqueous electrolytes due to severe hydrogen evolution reaction (HER), which is more serious than the commonly studied Zn metal anodes. Moreover, the mechanism of HER side reactions has remained unclear. Herein, we design a series of Mn‐P alloying anodes by precisely regulating their energy band structures to mitigate the HER issue. It is found that the serious HER primarily originates from the spontaneous Mn‐H2O reaction driven by the excessively high HOMO energy level of Mn, rather than electrocatalytic water splitting. Owing to a reduced HOMO energy level and enhanced electron escape work function, the MnP anode achieves an evidently enhanced cycle durability (over 1000 hours at a high current density of 5 mA cm‐2). The MnP||AgVO full cell with an N/P ratio of 4 exhibits better rate capability and extended cycle life (7000 cycles) with minimal capacity degradation than the cell using metallic Mn anode (less than 100 cycles). This study provides a practical approach for developing highly durable aqueous Mn ion batteries

Porphyrinoid-Functionalized ZnO Nanoflowers for Visible Light-Enhanced and Selective Benzylamine Detection at Room Temperature.

Functionalization of hybrid organic molecules as layers on ZnO nanoflowers (NFs) gives an excellent combination of sensing toward visible light and vapors of various volatile organic compounds (VOCs). In this work, hybrid organic molecules functionalized ZnO NFs were utilized for the photoinduced detection of benzylamine at room temperature. The ZnO NFs were synthesized via a facile solution route and functionalized with four different porphyrin-conjugated molecules namely (i) pyrene-porphyrin (PP), (ii) pyrene- porphyrinato zinc (ZnPP), (iii) triphenylamine- porphyrin (TP) and (iv) triphenylamine- porphyrinato zinc (ZnTP). The diameter of the flower-like structure was found to be ∼3.2 μm with the thickness of petals being ∼24.1 nm. The gas adsorption performance of the functionalized ZnO NFs on light activation at room temperature was studied by using a scanning Kelvin probe (SKP) system. The improved adsorption properties of the samples can be attributed to the heterojunctions and light activation. In particular, an enhanced response of ZnTP functionalized ZnO (ZnTPZ) toward benzylamine was observed. Further, static gas sensing experiments using ZnTPZ under various concentrations (1, 3, 5, 10, 15, and 25 ppm) of benzylamine vapors both in dark and visible light conditions have exhibited a linear increase in the response. The selectively enhanced response of ZnTPZ compared to that of pristine ZnO was thus confirmed at 1 ppm of benzylamine. The sensitivity and limit of detection of the ZnTPZ sensor were calculated to be 0.0292 ppm-1 and 197 ppb, respectively. The coordination metal (Zn) has helped in effective charge transfer between benzylamine and ZnTPZ by providing additional active sites for interactions. Also, density functional theory calculations demonstrated the role of the hybrid organic molecules on the sensor surface in improving gas adsorption. Further, fresh cabbage was utilized for real sample analysis with the proposed sensor under visible light illumination conditions, and a linear response was obtained for low ppm evaluation at room temperature. Overall, the obtained results suggest the development of novel ZnTPZ-based light-activated gas sensors for low ppm benzylamine detection at room temperature. These kinds of sensors can be used to track the freshness of vegetables as they are transported from farms to commercial outlets.

Synergistic Cationic Shielding and Anionic Chemistry of Potassium Hydrogen Phthalate for Ultrastable Zn─I2 Full Batteries.

Electrolyte additives are investigated to resolve dendrite growth, hydrogen evolution reaction, and corrosion of Zn metal. In particular, the electrostatic shielding cationic strategy is considered an effective method to regulate deposition morphology. However, it is very difficult for such a simple cationic modification to avoid competitive hydrogen evolution reactions, corrosion, and interfacial pH fluctuations. Herein, multifunctional additives of potassium hydrogen phthalate (KHP) based on the synergistic design of cationic shielding and anionic chemistry for ultrastable Zn||I2 full batteries are demonstrated. K cations, acting as electrostatic shielding cations, constructed the smooth deposition morphology. HP anions can enter the first solvation shell of Zn2+ for the reduced activities of H2O, while they remain in the primary solvation shell and are finally involved in the formation of SEI, thus accelerating the charge transfer kinetics. Furthermore, by in situ monitoring the near-surface pH of the Zn electrode, the KHP additives can effectively inhibit the accumulation of OH- and the formation of by-products. Consequently, the symmetric cells achieve a high stripping-plating reversibility of over 4500 and 2600 h at 1.0 and 5mA cm-2, respectively. The Zn||I2 full cells deliver an ultralong term stability of over 1400 cycles with a high-capacity retention of 78.5%.

Highly Reversible Zn Anode Design Through Oriented ZnO(002) Facets.

The practical implementation of aqueous Zn-ion batteries presents formidable hurdles, including uncontrolled dendrite growth, water-induced side reactions, suboptimal Zn metal utilization, and intricate Zn anode manufacturing. Here, large-scale construction of a highly oriented ZnO(002) lattice plane on Zn anode (ZnO(002)@Zn) with thermodynamic inertia and kinetic zincophilicity is designed to address such problems. Both theoretical calculations and experiment results elucidate that the ZnO(002)@Zn possesses high Zn chemical affinity, hydrogen evolution reaction suppression, and dendrite-free deposition ability due to the abundant lattice oxygen species in ZnO(002) and its low lattice mismatch with Zn(002). These features synergistically promote ion transport and enable homogeneous Zn deposition. Consequently, the ZnO(002)@Zn anode displays a stable and prolonged cycling lifespan exceeding 500h even under a larger depth of discharge (85.6%) and realizes an impressive average Coulombic efficiency of 99.7%. Moreover, its efficacy is also evident in V2O5-cathode coin cells and pouch cells with not only high discharge capacity but also exceptional cycling stability. This integrated approach presents a promising avenue for addressing the challenges associated with Zn metal anodes, thereby advancing the prospects of aqueous Zn-ion battery technologies.

Selective Sorption of Noble Metals on Polymer Gel Modified with Ionic Liquid.

The solid phase extraction of Au, Ir, Pd, Pt, and Rh on a polymer gel modified with ionic liquid containing methylimidazolium groups (MIA-PG) has been investigated. The positively charged surface of the sorbent is highly suitable for the sorption of stable chlorido complexes of the studied analytes, while the retention of base metals Cu, Fe, Ni, Zn, and Mn is negligible. Optimization experiments performed showed that, at 0.05 M HCl, the degree of sorption of Au, Ir, Pd, and Pt is above 95%, and only for Rh, the maximum degree is 65%; complete elution is achieved in the mixture of thiourea in HCl. The results obtained from the equilibrium adsorption studies are fitted in various adsorption models, such as Langmuir and Freundlich, and the model parameters have been evaluated. The kinetics analysis indicated that the adsorption of Au, Ir, Pd, Pt, and Rh onto the sorbent follows the pseudo-second-order model. Intraparticle diffusion and ion exchange reactions were the rate-limiting steps. Analytical procedures were developed for Pd, Pt, and Rh determination in road dust and soil and for Au determination in copper ore and copper concentrate. The procedures are validated by the analysis of certified reference materials. Analytical figures of merit confirmed their applicability in routine laboratory practice.

Synthesis of ZnO NWs via Thermal Evaporation Technique

Zinc oxide nanowires ZnONWs were successfully synthesized on glass slides. The synthesis was conducted firstly by the deposition of 12 µm a thin film of Zn metal by thermal evaporation. Secondly,the coated film was annealed at a temperature of 600 ºC in air for four hours to grow the ZnO nanowires. It have been observed that the produced nanowires were grown in a vertical orientation and having a high density, very long, and a minimal aspect ratio. The crystal structure and morphology of ZnO nanowires were investigated with X-ray diffraction (XRD) and scanning electron microscopy (SEM). The UV-visible spectrophotometer was also used to calculate the optical parameters from the absorption spectrum and show a band gap energy around 3.25 eV. The crystal structure of the material was revealed to be polycrystalline with a preferred orientation in the direction of [101]. Small average crystallite size was calculated about 17nm The wires can be measured to have a length of around 10 µm with diameters ranging from 50 to 100 nm. This could be used for gas sensor applications. In addition, this ZnONWs structure has a maximum transmittance (100%) which can be a good candidate for many optoelectronic apllications.

Occupational exposure assessment of heavy metals in human scalp hair among tannery workers in Bahir Dar, Ethiopia: Indication of pollution

Ethiopia, is one of the African countries, has immense potential for skins and hides for the leather industries, which will play a crucial role in converting nations into manufacturing-driven economies through industrialization. The chemicals applied in the tanning process are a serious concern for employees and the community if proper safety measures are not taken. The pollution status of employees working in Anbessa and Bahir Dar tannery factories was evaluated by collecting hair samples. After the hair samples washed with acetone, and deionized water, the hair samples were digested with 4 mL of HNO3 and 2 mL of HClO4 for 1:30 h at 250 °C. The levels of metals (Cr, Pb, Zn, Cu, Ni, and Cd) were subsequently analyzed using a Flame Atomic Absorption Spectrophotometer (FAAS). The mean concentrations of Cu, Ni, Zn, Pb, and Cr in the Anbessa tannery factory workers were 17.34–22.75, 16.38–35.03, 235.4–369.2, 30.46–67.31, and 97.56–189.18, respectively, in the various working departments of the factory. Similarly, the concentrations of Cu, Ni, Zn, Cd, Pb, and Cr in the hair of Bahir Dar tannery workers were 30.1–105.9, 17.88–62.20, 216.9–762.1, 0.35–5.21, 33.42–91.42, and 118.5–305.7, respectively. Chromium was found to be the most accumulated metal next to Zn with in both tannery workers that highlighted significant occupational health risks. The principal component analysis (PCA) analysis provide an insights into the interactions between occupational factors and metal exposure. In conclusion, the results of hair analysis from the employees of tannery factories indicates alarming levels of metal exposure, especially for zinc and chromium, which might pose health problems in long time exposure. Thus, it's critical to monitor occupational activities that can harm human health and the environment.

Novel nanoliter spray enhanced microwave plasma ionization mass spectrometry for the simultaneous detection of heavy metals and organic plasticizers in soil: A case study in a lead-acid battery industrial park

Soil pollution is predominantly attributed to the presence of heavy metal elements and organic compounds; However, current detection methodologies are restricted to the identification of only one of these two sources at a time. A novel analytical approach, known as nanoliter spray enhanced microwave plasma ionization mass spectrometry (Nano-Spray-EMPI-MS), has been developed to facilitate the simultaneous detection of both heavy metals and organic pollutants in soil samples. This technique is characterized by its requirement for minimal sample volumes, thereby allowing for efficient and rapid analysis. The research concentrated on the simultaneous analysis of five heavy metals (Pb, Zn, Cu, Cr, and Ni) and three major phthalates (PAEs), specifically DEHP, DBP, and DMP. The detection and quantification limits for the heavy metals were established to be between 0.16-0.57 and 0.53–1.88 μg L−1, respectively, while the limits for the PAEs ranged from 0.02 to 0.05 and 0.07–0.16 μg L−1. Validation of the method's efficacy in soil detection demonstrated recovery rates of 90.9 %–105.7 % for heavy metals and 89.4 %–97.2 % for PAEs. The application of this method analyzing soil samples collected from an area adjacent to a lead-acid battery industrial park in China revealed varying levels of contamination by both heavy metals and PAEs. Notably, Lead contamination was found to be the most pronounced, with a peak concentration of 862.5 mg kg−1 and a correspondingly high pollution index. These findings are significant for evaluating local ecological risks, pinpointing sources of pollution, and formulating effective pollution management strategies in the region.

Air pollution tolerance and metal accumulation potential of some plant species growing in educational institutions of Amritsar, India.

Poor air quality in urban areas increases the exposure of individuals to air pollutants. Hence, it becomes mandatory to grow such plant species that have more potential to tolerate air pollution and can aid in its mitigation. Air pollution tolerance index (APTI) and anticipated performance index (API) are two indices that help in scientific evaluation of plant species before recommending them for plantation. In this study, six plant species from three educational institutions of Amritsar city were screened for their tolerance and performance against air pollution as well as for their capability to act as accumulators of nine metals viz., aluminium (Al), chromium (Cr), cobalt (Co), copper (Cu), iron (Fe), manganese (Mn), nickel (Ni), lead (Pb) and zinc (Zn). On the basis of APTI, Cassia fistula (C. fistula) was categorized as a tolerant species while Alstonia scholaris (A. scholaris), Cascabela thevetia (C. thevetia), Monoon longifolium (M. longifolium), Pongamia pinnata (P. pinnata) and Syzygium cumini (S. cumini) were categorized as intermediately tolerant plant species. API results suggested that A. scholaris, C. fistula, M. longifolium, P. pinnata and S. cumini should be planted for air pollution mitigation. Geo-accumulation Index (Igeo) results showed that soil samples were moderately contaminated with three (Pb, Cu and Zn) metals. Bioaccumulation factor (BAF), for all metals among six plant species, was found to be less than one implying that these plants were absorbers of metals. Metal Accumulation Index (MAI) indicated that C. thevetia, C. fistula and P. pinnata exhibited relatively higher potential for metal accumulation.