Metal Loading Research Articles

Potentially toxic elements concentration and distribution in soils around artisan workshops in Ago-Iwoye, Southwestern Nigeria

Background/IntroductionAnthropogenic activities, including those carried out by artisans, have been confirmed to be one of the various means by which potentially toxic elements (PTE) are introduced into the soil. This study aims to determine the PTE concentration and distribution in soils around artisans workshops in Ago-Iwoye, southwestern Nigeria. MethodsTwenty (20) soil samples comprising ten (10) samples from soil around auto-mechanic workshops, six (6) from soils around vulcanizer workshops and four (4) from soils around welder workshops were collected and analyzed for elemental concentration using Inductively Coupled Plasma Mass Spectrometry (ICP-MS). ResultsElemental analysis revealed the following trend for selected metals in auto-mechanic, vulcanizing and welding workshops, respectively: Ba (60–100, 100–200 and 130–590 mg.kg−1); Co (10–47, 8–19 and 15–37 mg.kg−1); Cr (29–161, 22–95 and 57–272 mg.kg−1); Cu (28–123, 16–100 and 88–486 mg.kg−1); Ni (11–33, 7–29 and 34–112 mg.kg−1); Pb (17–75, 12–77 and 36–677 mg.kg−1); Sc (2–16, 1–7 and 2–8 mg.kg−1); Sr (13–55, 17–72 and 33–91 mg.kg−1); V (35–212, 20–117 and 40–103 mg.kg−1) and Zn (82–684, 70–548 and 314–3240 mg.kg−1). Geochemical assessment using contamination factor, and geo-accumulation index showed that the artisanal workshops exhibited significant contamination levels for metals such as Ba, Cu, Ni, Pb, Sr, and Zn and the contamination level varied across the artisan workshops with soils around welders workshops showing highest contamination. ConclusionContamination indices revealed the artisan workshops have varying contribution to the metal load in the area and Pollution Load Index (PLI) indicated a decline in soil quality across all artisanal workshops with welding workshops revealing the highest anthropogenic contribution of PTE to the soil.

Solid hydrogen storage with palladium-graphene composites: Synthesis, characterization, and mechanistic insights

Efficient and safe hydrogen storage is a pivotal challenge for the advancement of hydrogen energy technologies. To address this, the engineering of high-performance solid-state hydrogen storage materials through the loading of transition metals (TM) on carbon-based solids has gained considerable interest. However, the mechanics for TM such as Palladium that bolster hydrogen storage have not well addressed yet. This work presents hydrogen absorptions with metal Pd nanoparticles loaded on reduced graphene oxide (Pd-rGO), including material preparation, structural characterization, hydrogen storage performance, and quantum chemical mechanistic insights. A simple material synthesis strategy has been explored and Pd-rGO composites are successfully prepared with graphite powder as raw materials by an easy reduction-oxidation process. Then, Pd-rGO composites are characterized using X-ray diffraction, Fourier-transform infrared spectroscopy, Raman, transmission electron microscopy, and nitrogen adsorption-desorption isotherms methods to clarify the detailed structural characteristics of Pd-rGO with different loading amounts. It is found that Pd nanoparticles with an average particle size of 10 nm are uniformly dispersed on the surface of rGO. The materials have high defect severity and increased specific surface areas with Pd loading. The hydrogen adsorption capacity of Pd-rGO can be increased by 64 % compared with that without Pd loading due to the hydrogen spillover effect. In addition, the intensification mechanism of hydrogen storage of Pd-rGO composites is further understood by using density functional theory calculations and surface interaction analysis.

High-loading Au nanoparticles on carbon by engineering surface charge and specific surface area of substrates

Energy transition towards net-zero society calls for utilization of renewable power to drive CO2 conversion in an efficient electrochemical way. The development of a commercial CO2 electrolyzer with positive tech-eco effect calls for active and durable electrocatalysts. High-loading gold on carbon (Au/C) with reduced particle size is the prerequisite for the highly-selective and highly energy-efficient CO production in such a CO2 electrolyzer, but a scalable synthetic method is missing. With combined control of ligand, substrate and pH value, Au/C catalysts with particle size within 5 ​nm and metal loading of 40 ​wt% and 60 ​wt% are synthesized on low and high surface-area carbon, respectively. We also provide a thorough investigation of the effect of the ligand type, surface charge of gold nanoparticles (Au NPs) and surface area of carbon substrate on the loading limit of Au/C.

Impact of brewery sludge application on heavy metal build-up, translocation, growth and yield of bread wheat (Triticum aestivum L.) crop in Northern Ethiopia

In a field study, the impact of different levels of brewery sludge (BS) enrichment on Triticum aestivum L. (wheat plants) was examined in terms of growth, yield, heavy metal absorption, and potential health risks linked to plant consumption. Using a randomized complete block design with seven treatments and three blocks, the study showed that applying up to 12 t ha−1 brewery sludge significantly improved all agronomic parameters (except harvest index) compared to control and mineral-fertilized soil. Heavy metal translocation was generally low, except for Cu and Pb. The sequence of heavy metal translocation was Cu > Pb > Cd > Ni > Zn > Mn > Cr from soil to spikes and Cu > Zn > Mn > Pb > Ni > Cd > Cr from soil to grain. Heavy metal loads were mostly higher in roots than in the above-ground crop parts. The target hazard quotient (THQ), hazard index (HI), and target cancer risk (TCR) within wheat grain remained within safe limits for all BS treatments. Consequently, consuming this wheat grain is considered safe regarding heavy metals. Thus, utilizing brewery sludge at 12 t ha−1 as a fertilizer for wheat production and as an alternative method for sludge disposal is plausible.

Low concentration adsorption of ammonia using metal halide loaded biogas residue-based carbon materials

Treating wastewater with elevated ammonia nitrogen levels in garbage treatment plants is a global concern, with blow-off recognized as an efficient process for nitrogen removal. However, this method generates low-concentration ammonia, presenting a challenge for adequate recovery. This study addresses this issue by impregnating metal halides onto K2CO3-activated biogas residue to create composite materials tailored for adsorbing low-concentration ammonia. We systematically investigated the impact of activation parameters, metal halide type, loading capacity, and environmental conditions on the adsorption properties of the materials. Notably, at an activation temperature of 700 °C, utilizing copper chloride with a loading capacity of 30 %, the material exhibited a saturation adsorption capacity of 29.32 mg/g for 200 ppm NH3, with a breakthrough time of 45.6 min, significantly surpassing the untreated sample and demonstrated excellent regeneration performance. SEM, BET, and FTIR analyses revealed that the material provided dispersion sites for metal halides, promoted the complexation of metal halides and ammonia and retained pores for ammonia diffusion, thereby enhancing adsorption efficiency. This innovative approach contributes to waste utilization and ensures efficient ammonia recovery through metal halide-ammonia complexation.

Evaluation of Heavy Metal Contamination and Associated Human Health Risk in Soils around a Battery Industrial Zone in Henan Province, Central China

This research investigated the contamination characteristics, sources, and health risks of five metals in soils from two villages named DK and SXC, downstream from a battery industry hub in Xinxiang city, Henan Province, China. The average concentrations of Cd, Pb, Ni, Cu, and Zn in DK were 5.93, 41.31, 71.40, 62.20, and 115.83 mg/kg, respectively, and in SXC were 2.04, 30.41, 41.22, 36.18, and 96.04 mg/kg, respectively. The single factor pollution index (Pi) revealed a consistent descending order of Cd > Cu > Zn > Ni > Pb in DK and SXC. The geo-accumulation index (Igeo) indicated that the Cd pollution in DK was extreme, and in SXC was at a heavy to extreme level. The potential ecological risk index (PERI) indicated that Cd presented a significantly high ecological risk while it was low for other metals. Principal component analysis classified them into the anthropogenic origin of Cd and common mixed origin of others. The elevated levels and pollution load of heavy metals with closer proximity to the battery factory imply that the factory is a probable source of contamination. Overall, the health risks posed by heavy metals were more pronounced for local children compared to adults, with Cd being the primary contributor to both pollution and health risks. This investigation provides a crucial basis for the heavy metal pollution management and related risk prevention in areas affected by electronic waste irrigation.

Mullite-like SmMn2O5-Derived Composite Oxide-Supported Ni-Based Catalysts for Hydrogen Production by Auto-Thermal Reforming of Acetic Acid.

The x%Ni/Sm2O3-MnO (x = 0, 10, 15, 20) catalysts derived from SmMn2O5 mullite were prepared by solution combustion and impregnation method; auto-thermal reforming (ATR) of acetic acid (HAc) for hydrogen production was used to explore the metal-support effect induced by Ni loadings on the catalytic reforming activity and product distribution. The 15%Ni/Sm2O3-MnO catalyst exhibited optimal catalytic performance, which can be due to the appropriate Ni loading inducing a strong metal-support interaction to form a stable Ni/Sm2O3-MnO active center, while side reactions, such as methanation and ketonization, were well suppressed. According to characterizations, Sm2O3-MnO mixed oxides derived from SmMn2O5 mullite were formed with oxygen vacancies; nevertheless, loading of Ni metal further promoted the formation of oxygen vacancies, thus enhancing adsorption and activation of oxygen-containing intermediate species and resulting in higher reactivity with HAc conversion near 100% and hydrogen yield at 2.62 mol-H2/mol-HAc.

Metal mobilization from thawing permafrost to aquatic ecosystems is driving rusting of Arctic streams

Climate change in the Arctic is altering watershed hydrologic processes and biogeochemistry. Here, we present an emergent threat to Arctic watersheds based on observations from 75 streams in Alaska’s Brooks Range that recently turned orange, reflecting increased loading of iron and toxic metals. Using remote sensing, we constrain the timing of stream discoloration to the last 10 years, a period of rapid warming and snowfall, suggesting impairment is likely due to permafrost thaw. Thawing permafrost can foster chemical weathering of minerals, microbial reduction of soil iron, and groundwater transport of metals to streams. Compared to clear reference streams, orange streams have lower pH, higher turbidity, and higher sulfate, iron, and trace metal concentrations, supporting sulfide mineral weathering as a primary mobilization process. Stream discoloration was associated with dramatic declines in macroinvertebrate diversity and fish abundance. These findings have considerable implications for drinking water supplies and subsistence fisheries in rural Alaska.

Multimetal exposure: Challenges in diagnostics, prevention, and treatment.

Extensive use of heavy metals has posed a serious concern for ecosystem and human too. Heavy metals are toxic in nature and their accumulation in human body causes serious disorders such as neurological disease, cardiac disease, gastrointestinal problems, skin disorders, reproductive disease, lungs diseases, and so on. Furthermore, heavy metals not only affect the human health but also have a negative impact on the economy. In the current review, we have elaborated the impact of heavy metal exposure on human health and socioeconomics. We have discussed the molecular mechanism involved in the heavy metal-induced human disorders such as oxidative stress, neuroinflammation, and protein misfolding. Finally, we discussed the preventive measure and treatment strategy that could counter the negative effects of heavy metal intoxications. In conclusion, there is a substantial correlation between heavy metals and the onset and advancement of several health issues. Chelation treatment could be a useful tactic to lessen the toxic metal load and the difficulties that come with it.

IrO2 Oxygen Evolution Catalysts Prepared by an Optimized Photodeposition Process on TiO2 Substrates.

Preparing high-performance oxygen evolution reaction (OER) catalysts with low precious metal loadings for water electrolysis applications (e.g., for green hydrogen production) is challenging and requires electrically conductive, high-surface-area, and stable support materials. Combining the properties of stable TiO2 with those of active iridium oxide, we synthesized highly active electrodes for OER in acidic media. TiO2 powders (both commercially available Degussa P-25® and hydrothermally prepared in the laboratory from TiOSO4, either as received/prepared or following ammonolysis to be converted to titania black), were decorated with IrO2 by UV photodeposition from Ir(III) aqueous solutions of varied methanol scavenger concentrations. TEM, EDS, FESEM, XPS, and XRD measurements demonstrate that the optimized version of the photodeposition preparation method (i.e., with no added methanol) leads to direct deposition of well-dispersed IrO2 nanoparticles. The electroactive surface area and electrocatalytic performance towards OER of these catalysts have been evaluated by cyclic voltammetry (CV), Linear Sweep Voltammetry (LSV), and Electrochemical Impedance Spectroscopy (EIS) in 0.1 M HClO4 solutions. All TiO2-based catalysts exhibited better mass-specific (as well as intrinsic) OER activity than commercial unsupported IrO2, with the best of them (IrO2 on Degussa P-25® ΤiO2 and laboratory-made TiO2 black) showing 100 mAmgIr-1 at an overpotential of η = 243 mV. Chronoamperometry (CA) experiments also proved good medium-term stability of the optimum IrO2/TiO2 electrodes during OER.

Spatiotemporal and multi-isotope assessment of metal sedimentation in the Great Lakes

This study investigates spatiotemporal dynamics in metal sedimentation in the North American Great Lakes and their underlying biogeochemical controls. Bulk geochemical and isotope analyses of n = 72 surface and core sediment samples show that metal (Cu, Zn, Pb) concentrations and their isotopic compositions vary spatially across oligotrophic to mesotrophic settings, with intra-lake heterogeneity being similar or higher than inter-lake (basin-scale) variability. Concentrations of Cu, Zn, and Pb in sediments from Lake Huron and Lake Erie vary from 5 to 73 mg/kg, 18–580 mg/kg, and 5–168 mg/kg, respectively, but metal enrichment factors were small (<2) across the surface- and core sediments. The isotopic signatures of surface sediment Cu (δ65Cu between −1.19‰ and +0.96‰), Zn (δ66Zn between −0.09‰ and +0.41‰) and Pb (206/207Pb from 1.200 to 1.263) indicate predominantly lithogenic metal sourcing. In addition, temporal trends in sediment cores from Lake Huron and Lake Erie show uniform metal concentrations, minor enrichment, and Zn and Pb isotopic signatures suggestive of negligible in-lake biogeochemical fractionation. In contrast, Cu isotopic signatures and correlation to chlorophyll and macronutrient levels suggest more differentiation from source variability and/or redox-dependent fractionation, likely related to biological scavenging. Our results are used to derive baseline metal sedimentation fluxes and will help optimize water quality management and strategies for reducing metal loads and enrichment in the Great Lakes and beyond.

Machine learning-driven prediction of phosphorus removal performance of metal-modified biochar and optimization of preparation processes considering water quality management objectives

Developing an optimized and targeted design approach for metal-modified biochar based on water quality conditions and management is achievable through machine learning. This study leveraged machine learning to analyze experimental data on phosphate adsorption by metal-modified biochar from literature published in Web of Science. Using six machine learning models, the phosphate adsorption capacity of biochar and residual phosphate concentration were predicted. After hyperparameter optimization, the gradient boosting model exhibited superior training performance (R2 > 0.96). Metal load quantity, solid–liquid ratio, and pH were key factors influencing adsorption performance. Optimal preparation parameters indicated that Mg-modified biochar achieved the highest adsorption capacity (387–396 mg/g), while La-modified biochar displayed the lowest residual phosphate concentration (0 mg/L). The results of verification experiments based on optimized process parameters closely aligned with model predictions. This study introduces a new machine learning–based approach for tailoring biochar preparation processes considering different water quality management objectives.

Improvement of hydrogen production via aqueous phase reforming of glycerol with Ni-Co catalysts synthesized through controlled urea matrix combustion

The effect of synthesis variable control during the combustion of urea in solution to obtain a Ni-Co/γ-Al2O3 catalyst with a low metallic loads for producting hydrogen by reforming glycerol was studied. Catalysts with the same urea/metal molar ratio but synthesized by controlled or uncontrolled urea matrix combustion were compared. It has been observed that adopting a urea/metal molar ratio between 2 and 6 and a heating rate of 10 °C∙min−1 results in a catalyst with an active surface and high Ni-Co interaction. This leads to significant improvements in H2 yield (from 34 to 50%), glycerol conversion (from 35 to 50%), and H2 selectivity (from 96 to 99%), while maintaining stability during 420 min of reaction. The repeatability of controlled synthesis has shown differences in results of less than 2%. Controlled synthesis is an attractive approach for scaling up the process for treating glycerinous waters, effluents in biodiesel plants.

Effects of the Type and Loading of Rare-Earth Metals (Pr, Yb, Ho) on the para-Selectivity of HTsVM Zeolite in Toluene Ethylation

Effects of the Type and Loading of Rare-Earth Metals (Pr, Yb, Ho) on the para-Selectivity of HTsVM Zeolite in Toluene Ethylation

Sewage sludge co-gasification in a pilot-scale two-stage fluidized bed gasifier for improved hydrogen production: Effects on sewage sludge moisture, metal species, and metal loading amount

Theabundant mineral olivine was applied as second-stage-gasifier bed materials to increase the H2 content in the syngas produced during the co-gasification of the sewage sludge and the simulated municipal solid waste. Regardless of the second-stage bed material used, the hydrogen-to-syngas ratio in the syngas output from the second stage increased when the S/B ratio increased from 0.02 to 0.13. This demonstrates that adding steam enhances the hydrogen-to-syngas ratio in the second-stage syngas. Under the same S/B conditions, the H2 content in the syngas varied when the original and modified olivine were separately used as bed materials in the second-stage gasifier. The H2 content was 23.12 mol.% when the original olivine was used and increased to 25.27 and 26.99 % mol.% when the olivine was respectively impregnated with 1 wt% Ni and 1 wt% Fe. These results evidenced that Ni and Fe could efficiently catalyzed the co-gasification of sludge and simulated municipal solid waste and improved the hydrogen production efficiency.

Experimental study of low-temperature combustion performance in hydrogen/air mixtures over Pt–Cu/HZSM-5/cordierite bimetallic catalysts

Catalytic combustion provides a feasible technology to effectively avoid NOx formation due to the high temperature in the process of hydrogen combustion. Recently, the development of efficient and affordable catalysts has attracted extensive attention as the cost of noble metals remained high. In this study, a list of cordierite monolithic catalysts with low noble metal loading are prepared by introducing the appropriate amount of transition metals (Mn, Cu, Fe, Co, and Ce), and their catalytic performance are further investigated. On this basis, the study on catalytic stability and kinetic is carried out, and the synergistic interaction between the bimetals is revealed with comprehensive characterization methods. The results show that Cu could promote the reaction rate of the Pt-based catalyst which show the best catalytic performance with the Cu loading of 1 g/L. The ignition temperature T10 is 58.5 °C, and the burnout temperature T100 is 100 °C, with activation energy as low as 44.00 kJ/mol. The enhancement of the catalytic performance is attributed to the interaction between the bimetallic elements. On the one hand, the valence state of Cu and Pt is changed, and on the other hand the dispersion of Pt get improved, which contributed to the catalytic reaction rate.

The competition of heavy metals between hyporheic sediments and microplastics of driving factors in the Beiluo River Basin

Both sediments and microplastics (MPs) are medias of heavy metals (HMs) in river ecosystems. This study investigated HMs (Mn, Cr, V, As, Cu, Co, Cd, Pb, and Ni) concentration and driving factors for competitive enrichment between hyporheic sediments versus MPs. The medias basic characteristics indicated that the sediments were mostly sand and rich in Fe2O3; three polymer types were identified, with blue, fragment, less than 500 µm being the main types of MPs. The results have shown that the average content of extracted HMs in MPs was much higher than that of the same metals accumulated in sediments. HMs in sediments and MPs reached heavily polluted at some points, among which As and Cd were ecological risks. Electrostatic adsorption and surface complexation, and biofilm-mediated and organic matter complexation were the interaction mechanism of HMs with sediments and MPs. Further, the driving factors affecting the distribution of HMs in the two carriers were analyzed by multivariate statistical analysis. The results demonstrated that carrier characteristics, hydrochemical factors, and the inherent metal load of MPs were the main causes of the high HMs content. These findings improved our understanding of HMs fate and environmental risks across multiple medias.

Valorization of agroindustrial orange peel waste during the optimization of activated carbon–multiwalled carbon nanotubes–zinc oxide composites used in the removal of methylene blue in wastewater

Activated carbons (AC) produced from agroindustrial orange peel (OP) wastes and/or commercial multi–walled carbon nanotubes (MWCNTs) were modified with ZnO nanoparticles in different amounts (15 and 30 wt–%) for the removal of methylene blue in aqueous solutions. The MWCNTs functionalization was carried out by typical procedure in acid medium using a ratio of 3:1 (HNO3/H2SO4). A batch adsorption analysis was carried out evaluating different parameters: MB concentration from 40 to 100 mg L–1; pH values between 4 and 10 and adsorption time that varied from 1 to 48 h. The modified materials were characterized through the techniques XRD, FTIR, BET, TGA, SEM and UV–vis. The results showed an adequate dispersion of ZnO NPs on the carbon surfaces with a typical flower–like morphology this type of shape developed micropores that facilitate adsorption phenomena. Under the evaluation conditions, 20 mg of carbon–based materials can remove up to 89.5 ± 4.47 % of MB (80 ppm) after 24 h of exposure at a regulated pH of 8. The equilibrium adsorption data were better fitted by a Langmuir isotherm (R2 = 0.9999) than the Freundlich model (R2 = 0.9366); showing in the best case a maximum adsorption capacity of 1250 mg g−1 for both materials with 30 wt–% of ZnO NPs (AC–MWCTs or MWCNTs). Experimental data also suggest that the most likely mechanism is chemisorption followed by physical adsorption. Then, the compounds with 30 wt–% metal loading (ZnO NPs), AC–MWCNTs–ZnO or MWCNTs–ZnO, displayed the most interesting properties for MB dye removal. AC–ZnO compounds can also remove about 88.75 ± 4.43 % of MB, demonstrating that it can also be a facile and low–cost method to improve the surface area in carbonaceous structures by promoting a strong interaction with the ZnO NPs, which in turn helps to remove contaminants in water efficiently.

Pseudo-total metal loads in dusts and soils of the steel city and coal capital of India: source apportionment and assessment of human health and ecological risks

Pseudo-total metal loads in dusts and soils of the steel city and coal capital of India: source apportionment and assessment of human health and ecological risks

TiO2 nanotubes modification by photodeposition with noble metals: Characterization, optimization, photocatalytic activity, and by-products analysis

Self-organized TiO2 nanotubes (TNTs) with 4 µm length were obtained by anodization method and calcined to obtain anatase crystallite phase. The photocatalysts were further decorated with Au, Ag, Pt or Pd nanoparticles (NPs), varying the metal loads (0.50, 0.75, 1, 2 and 5 mol%) by photodeposition. The material characterization confirmed the presence of nanoparticles in the TNTs surface, signs of the localized surface plasmon resonance (LSPR) effect for some samples and a bandgap energy of 3.1–3.2 eV. Photoluminescence measurements also confirmed that most of the samples with metallic nanoparticles had the recombination of photogenerated carriers lowered due to the trapping effect of the deposited metal NPs. The photoactivity was evaluated by phenol degradation using UV-Vis or visible radiation. Under UV-Vis, the best samples (2 and 5 mol% of Au-TNTs and 0.75, 1, and 2 mol% of Pd-TNTs) led to 97% phenol removal in 60 min while pristine TNTs reached 92% removal. Under visible radiation, the pristine and the Au-TNTs led to about 3% removal, with the best sample being 2 mol% Pd-TNTs with 14% removal in 60 min. Similar results were obtained for 1 and 5 mol% Pd-TNTs (12% and 13% of phenol removal, respectively). The by-products analysis suggest different degradation mechanisms and it is observed different kinetic rates for different metal types, metal loads or types of radiation.