Ag Content Research Articles

Determination of silver ions in distilled water by stripping voltammetry at a Nafion-coated gold electrode in combination with quartz crystal microbalance and electrochemical impedance spectroscopy

Here, we propose a stripping voltammetric method for Ag+ ion determination in distilled water utilizing screen-printed Au electrodes coated with Nafion (Nafion/Au screen-printed electrodes). The concentration of Ag+ in pure water was determined by linear sweep voltammetry (LSV) after silver deposition on the Nafion/Au electrode. The anodic stripping peak current increased linearly with the concentration of Ag+ ion in the range from 1 ppm to 22 ppm. The LSV oxidative peak current was increased by extending the silver deposition time from 300 s to 500 s. Repetitive LSV measurements revealed satisfactory reproducibility of the Nafion/Au screen-printed electrodes. The detection mechanism was elucidated by recording mass changes of the Nafion/Au electrode with a quartz crystal microbalance (QCM), and by determining changes in the low-frequency capacitance of the Nafion/Au electrode by electrochemical impedance spectroscopy (EIS). The observed changes in mass and capacitance confirmed Ag+ accumulation and release processes at the Nafion/Au electrodes, in good agreement with stripping voltammetry. The combination of stripping voltammetry, QCM and EIS allowed a detailed characterization of the ion transfer, deposition and stripping processes at the Nafion/Au electrodes in presence of Ag+ ions. The Nafion/Au screen-printed electrode enabled voltammetric determination of low Ag+ concentrations in distilled water, without any sample pretreatment nor addition of supporting electrolyte.

Metal concentration in honeybees along an urbanization gradient in Central Mexico

Urbanization is rapidly increasing worldwide, leading to rising levels of pollution, one of the major drivers of environmental change; yet little is known about the relationship between urbanization intensity and pollution levels in pollinator taxa. Toxic metals are among the most common contaminants in urban environments, but few data exist on their presence in the flora and fauna of cities in Latin America, one of the world's most urbanized and biologically diverse regions. In this study, we used an urban-rural gradient approach to analyze the relationship between the concentrations of eleven metals present in adult honeybees (Apis mellifera) and the degree of urbanization within twelve landscapes in the metropolitan area of Pachuca, Hidalgo, which forms part of the megalopolis of Mexico City. Metal concentrations were compared with previously reported values contrasting honeybees from urban and rural areas after standardizing urbanization levels among published reports. The concentrations of Ag, Cr, Cu, and Zn in honeybees increased significantly with the degree of urbanization. Urbanization was not found to influence the levels of Al, Ba, Cd, Mn, and Sr in honeybees. The maximum concentrations of six metals in our urban sites (Al, Ba, Cd, Cu, Mn, and Sr) were higher than the maximum values reported for bees in other urban areas. The concentrations of two metals measured in our study (Cr and Zn) were within the range of values previously published for urban areas. Compared to other studies, we did not detect Pb in the body of honeybees. We conclude that the concentrations of Ag, Cr, Cu, and Zn present in honeybees are a quantitative reflection of the degree of urbanization in central Mexico. Our results highlight the need to monitor metal emission sources in this and other areas and investigate their effects on bees and other pollinator taxa.

Ag quantum dots-doped poly (vinyl alcohol)/chitosan hydrogel coatings to prevent catheter-associated urinary tract infections

The prevention of catheter-associated urinary tract infections (CAUTIs) significantly impacts the reduction of morbidity and mortality associated with the use of indwelling urinary catheters. This study focused on developing an antibacterial double network hydrogel coating for latex urinary catheters, which incorporated Ag quantum dots (Ag QDs) in a polyvinyl alcohol (PVA)-chitosan (CS) double network hydrogel matrix. The PVA-CS-Ag QDs, referred to as the PCA hydrogel coating exhibited excellent mechanical and physiochemical properties with controlled release of Ag QDs. The antibacterial properties of the PCA hydrogel-coated urinary catheters were studied against both gram-negative Escherichia coli (E. coli, ATCC25922) and gram-positive Staphylococcus aureus (S. aureus, ATCC29213). The continuous release of CS oligomers and Ag QDs from the hydrogel coating contributed to the synergistic antibacterial and antiadhesion effects. Measurements of the Ag release rate revealed that even after 30 days, the concentration of Ag QDs from the PCA hydrogel-coated urinary catheters remained significantly higher than the effective antibacterial concentration of the total Ag (0.1 μg·L−1). These results indicated that the PCA hydrogel coating not only efficiently prevented bacteria attachment, but also exhibited long-term antibacterial activity, thereby inhibiting biofilm formation. Furthermore, the PCA hydrogel-coated urinary catheter demonstrated excellent biocompatibility and hemocompatibility. Overall, this novel PCA hydrogel-coated urinary catheter, with its exceptional antibacterial properties, holds great potential in reducing the incidence of CAUTIs.

Ag QDs modified BiOCl/UiO-66-NH2 Z-scheme heterojunction for accelerated visible light-driven photocatalytic degradation of ciprofloxacin

Ag quantum dots (QDs) anchored on the surface of BiOCl/UiO-66-NH2 Z-scheme heterojunctions were synthesized and characterized by various techniques such as X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectra (UV–vis DRS), electrochemical impedance spectroscopy (EIS), and photoluminescence (PL). The effects of Ag QDs loading, pH values and co-existing anions on the photocatalytic performance were comprehensively analyzed. The results concluded that the Ag QDs modified catalysts exhibited excellent photocatalytic performance for the degradation of ciprofloxacin (CIP), especially, the catalyst with 5 % Ag QDs loading (referred to as ABU-5) achieved a degradation efficiency of 72 % within 120 min and the apparent reaction rate constant was 0.00538 min−1. The outstanding performance of the ABU-5 catalyst is attributed to the introduction of Ag QDs as electron transfer bridges, improving visible light absorption and enhancing charge transfer between BiOCl and UiO-66-NH2. Free radical trapping experiments and leaching tests were carried out to determine the contribution rates of reactive species to the degradation efficiency and the concentration of Ag+ in solution after the reaction. The possible degradation pathways of CIP by ABU-5 were investigated by gas chromatography-mass spectrometry (GC-MS).

Effect of trace silver on the conductivity and softening temperature of high conductivity and high heat resistance pure copper

As a conductor material for high-power electronic devices, pure copper requires both conductivity and softening temperature. The effects of 0% (7NCu), 0.015% (Ag150), 0.030% (Ag300), 0.045% (Ag450) and 0.059% (Ag590) Ag on the microstructure, conductivity and softening temperature of pure copper were studied. The results show that trace Ag can refine the microstructure of pure copper and improve the mechanical properties at room temperature and high temperature. The hardness values of 7NCu, Ag 150, Ag 300, Ag 450 and Ag 590 were 112, 119.06, 122.14, 123.54 and 125.68HV, respectively, and the softening temperatures were 195, 310, 336, 344 and 345 °C, respectively. At the same time, the conductivity of the samples with different Ag content was more than 100.5 %IACS. The similar structure of Ag and Cu has little effect on the conductivity. On the one hand, the trace Ag element soluble in the matrix causes lattice distortion, inhibits recrystallization nucleation and grain boundary migration. On the other hand, the Ag element is polarized at the grain boundary, which reduces the grain boundary energy, decreases the atomic diffusion and increases the recrystallization temperature.

Enhanced Schottky barrier engineering in silver-doped TiO2/p-Si heterojunctions: Insights into electrical behavior and charge carrier dynamics

Heterojunctions were fabricated through the deposition of silver-doped Titanium dioxide (Ag–TiO2) onto p-type crystalline silicon, employing the sol-gel technique. Electrical characterization was conducted with varying Ag concentrations. The investigation revealed that the Schottky barriers at each interface (Ag/TiO2 and Si/Ag), along with the built-in potential at the TiO2/p-Si junction, increase proportionally with the Ag concentration. This observed trend was attributed to the reduction in the TiO2 bandgap due to Ag incorporation, resulting in a concurrent shift in both valence and conduction bands. Consequently, there is a growth of the conduction energy discontinuity and a reduction in the valence one, facilitating hole diffusion while impeding electron transfer across the depletion layer. Furthermore, the introduction of Ag leads to a decrease in both electron and hole concentrations. However, Ag incorporation within the TiO2 matrix manifests as nanoparticles and clusters, resulting in a nonhomogeneous distribution of charge carriers across the sample. Impedance analysis indicates an increase in device resistance and a decrease in effective capacitance.

Genesis of the Kateba’asu gold deposit, Western Tianshan, China: Constraints from pyrite trace element, sulfur isotope, and quartz H-O isotopes

The Kateba’asu gold deposit, situated in the Western Tianshan of China, is one of the most significant discoveries in the world-class Tianshan gold belt. The deposit features two distinct mineralization styles. The early, subordinate skarn-type copper–gold mineralization occurs in the contact zone between monzogranite, diorite, and Silurian limestone, composed of garnet, diopside, epidote, chalcopyrite, pyrite, and gold. The later, primary lode-gold mineralization is hosted in the altered monzogranite characterized by pervasive quartz-pyrite-sericite-chlorite-K-feldspar alteration and a well-develped veining systems.Pyrite is the dominant sulfide mineral related to gold mineralization in the Kateba’asu gold deposit, with four types identified: Py0 from the early skarn copper–gold mineralization, and Py1 to Py3 from the later lode-gold mineralization. All types of pyrite are homogeneous and contain very low levels of lattice-bound gold. Py0 is euhedral and fine-grained, with relatively high Cu, Au, Co, and Ni contents, and displays a magmatic sulfur isotopic signature with δ34S ranging from 0.8 to 4.3 ‰. Py1 occurs as euhedral to subhedral, coarse-grained crystals within pyrite-quartz veins with higher concentrations of Co and Ni. Py2, which develops in the quartz-pyrite veins, is medium to coarse-grained and contains elevated levels of As, Cu, Zn, and Bi relative to Py1. Py3, found in polymetallic sulfide veins of the main lode-gold stage, is anhedral and medium to fine-grained with higher contents of As, Ag, Cu, Zn, Se, Te and lowest Co and Ni concentrations compared to Py1 and Py2. The positive correlations between Au-Te, Au-Bi, Au-Cu, and Pb-Bi across all pyrite types, along with the presence of visible gold in Py3, indicate that most gold occurs as micro-/nano-sized inclusions and as fissure gold. The δ34S values of Py1, Py2, and Py3 (7.6 to 11.8 ‰, 10.1 to 12.6 ‰, and 9.8 to 12.4 ‰, respectively) were attributed to an initial magmatic source and mixed with external sulfur subsequently from the wall rocks. The H and O isotopic compositions (δDH2O = −84.1 to −93.5 ‰; δ18OH2O = 1.8 to 6.6 ‰) of quartz from the lode-gold mineralization imply that ore-forming fluids were predominantly of magmatic origin, with a additional contribution from meteoric water. Taken together, a two-episode mineralization model was proposed for the formation of the Kateba’asu gold deposit. The early skarn mineralization stage is associated with the emplacement of diorite during the Early Carboniferous. In contrast, the subsequent lode-gold mineralization, occurring between the Late Carboniferous and Permian periods, represents a overprinted magmatic-hydrothermal gold system potentially linked to a deep-seated magmatic intrusion.

Sulfide trace element enrichments in the metamorphic basement-hosted Xinhua Pb-Zn-Cu vein-type deposit, eastern Guizhou province (SW China)

Cambrian carbonate formations are widespread in the western Hunan-eastern Guizhou (WHEG) region (southwestern China), which hosts many Mississippi Valley-Type (MVT) lead–zinc (Pb-Zn) deposits. Regional Pb-Zn mineralization is well developed in the low-grade metamorphic rocks of the basal Proterozoic Banxi Group. The mineralization is associated with quartz veins and generally distributed along NE-trending fault zones. Moreover, these deposits have an extensive distribution and high grade, and are associated with Cu-Ag endowment. However, geological and geochemical research on these Pb-Zn vein-type deposits is relatively limited, and their relationship with the regional MVT mineralization remains unclear. The representative Xinhua deposit in Danzhai district is selected as the study subject. We conducted in situ trace element analyses on the sphalerite and chalcopyrite from the various metallogenic stages, and compared them with published sphalerite trace element data from the MVT Pb-Zn deposits in the western Hunan-eastern Guizhou metallogenic belt. Seven orebodies in Xinhua Pb-Zn deposit have been discovered so far, with a metal resource of over 120,000 metric tonnes of Zn + Pb. Field geology and microscopic petrography have revealed two mineralization stages: An early-stage black sphalerite (Sp-I) followed by reddish-brown sphalerite (Sp-II) mineralization, which corresponds to the main chalcopyrite mineralization stage, and a later-stage light-yellow sphalerite (Sp-III), Cu ore-barren mineralization.LA-ICPMS data indicate that the sphalerite from Xinhua has similar trace element compositions to those from the MVT Pb-Zn deposits in the region. They are relatively enriched in Ga, Cd, and Ge, while depleted in Fe, Co, and Mn. Critical metal Ge and Ga are particularly enriched in sphalerite, especially in Sp-I (Ge max 937 ppm, Ga max 824 ppm). The substitution mechanism of Ge and Ga in sphalerite are likely 2Cu+ + Ge4+ ↔ 3Zn2+ and Cu+ + Ga3+ ↔ 2Zn2+. Indium and Sn are mainly present in Sp-I and Sp-III. Chalcopyrite contains Zn and Sn both exceeding 100 ppm. Contents of Se, Ag, In, and Sn in chalcopyrite are significantly higher than those in sphalerite. Calculation of the sphalerite trace element geothermometer (GGIMFis) suggests that the average sphalerite ore-forming temperatures are 164 °C (Sp-I), 156 °C (Sp-II), and 205 °C (Sp-III), implying medium- to low-temperature mineralization. This indicates a possible influx of high-temperature, in-bearing fluid during the late-stage mineralization.In summary, the faults-controlled vein-type Pb-Zn deposits (e.g., Xinhua) may have been products of the same Kwangsian orogeny as other strata bound MVT deposits, and the Xinhua deposit features two mineralization stages with multiple ore metal sources. During the ore-forming fluid ascent, some ore-forming materials may have precipitated in the fluid conduits. And exposed after the erosion of the shallower stratiform orebodies and strata. Consequently, the Xinhua Pb-Zn deposit represents the preserved ore-fluid conduit phase (in the basement strata) of the MVT mineralization.

Fluorinated B-72 hybrid silver doped modified nanoparticle as a coating for biological corrosion protection of ancient bricks

In this paper, a superhydrophobic organic-inorganic composite coating containing fluorinated B72 hybrid methyl-modified silica/(Ag doped TiO2) by hexamethyldisilazane (HMDS) (H-SiO2/Ag/TiO2) was prepared by means of a mild and an environmental friendly method. Transparency, adhesion, hardness tests and photocatalytic performance were measured to determine the content of Ag in TiO2 which the TiO2/AgNO3 ratio is 0.008 g/mL. The synthesized Ag/TiO2 nanoparticles were characterized by X-ray diffraction (XRD), Raman spectra and transmission electron microscope (TEM). The highest contact angle of coated ancient bricks was 148.66° and the color change value of ΔE⁎ before and after coating was <5 which is within an acceptable range. The physical properties such as apparent porosity and water vapor permeability (ΔMp) were studied. After weathering from acid, alkali, salt, water and ultraviolet radiation, the bricks coated by the composite coatings still have good hydrophobicity that the contact angle were >120° and minor degree of surface corrosion comparing with the ancient bricks. The inhibitory effect of the composite coating on Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), and that on algae (Chlamydomonas and Dunaliella) were studied through bacteriostasis test and algae comparative experiments, respectively. Finally, the mechanism of the composite coating on antibacterial and anti-algae was studied. The results showed that the appearance of the ancient bricks was not changed after coating, and the anti-weathering, antibacterial and anti-algae properties of the ancient transformation were increased.

Assessment of silver and graphitic carbon nitride doped cadmium selenide quantum dots as an efficient dye degrader and antibacterial agent: In silico molecular docking analysis

This study demonstrates the synthesis of co-precipitated cadmium selenide (CdSe) quantum dots (QDs) doped with (2 and 4 wt %) of silver (Ag) and fixed quantity of graphitic carbon nitride (g-C3N4) for catalytic as well as antibacterial potential with molecular docking (MD) analysis. Comprehensive characterizations investigated the structural composition, surface morphology, elemental composition, and optical properties. XRD revealed the multiple phases (hexagonal and cubic) of CdSe with a notable rise in the diffraction peaks intensity upon doping. The optical studies demonstrated the range of absorption peaks, which increased upon doping confirmed through band gap energies significantly altered. TEM study revealed that a sheet of g-C3N4 overlapped with CdSe QDs, and certain nanorod-like structures emerged after Ag doping. HR-TEM was employed for the d-spacing computation of prepared samples and exposed a decreasing trend as the Ag concentration increased. Furthermore, the catalytic activity (CA) performed against RhB dye showed maximum results in the acidic medium with a higher concentration of Ag into g-C3N4 doped CdSe. The efficient bactericidal efficacy was evaluated against S. aureus bacteria with the highest inhibition zone of 13.75 mm for 4% Ag doping, which was further explained by investigating their inhibitory effects on DNA gyrase and tyrosyl-tRNA synthetase via MD.

Enhancement of the photodegradation performance towards methylene blue and rhodamine B using AgxSn1–xO2 nanocomposites

In the present study, the structural properties, as well as the photodegradation performance of methylene blue (MB) and rhodamine B (Rh B) using hydrothermal synthesized AgxSn1–xO2 (0 ≤ x ≤ 1) nanocomposites were studied. The study was investigated using various techniques including EDS, XRD, FE-SEM, HR-TEM, photoluminescence spectroscopy, N2 adsorption-desorption, GC-MS, and a double-beam spectrophotometer. The tetragonal SnO2 phase dominates, while the cubic Ag2O phase appears at larger x ratios (x ≥ 0.5). The crystallite and particle sizes were slightly raised for a low Ag ratio but dramatically increased for higher x ratios. Different morphologies emerge depending on the composition, such as spherical and irregular particles for x = 0 and 1, sheet-like morphology for x = 0.05, 0.2, and 0.4, and worm-like morphology for x = 0.5. The maximum surface area was calculated using the BET method to be 358 and 354 m2/g for x = 0.2 and 0.4, respectively. The direct optical band gap depends on the x ratio and the crystallite size and equals 3.95eV and 3.70eV for x = 0 and x = 1, respectively. The synthesized AgxSn1–xO2 composites demonstrated excellent photodegradation efficiency (η) towards MB and Rh B. The majority of compositions had high η towards MB and the highest value of 99.6% was attained using Ag0.4Sn0.6O2 under the UV-visible irradiation for 1.5h. Also, synthetic composites demonstrated efficient photodegradation of Rh B, particularly for higher Ag content (η = 94.4% at x = 0.5). The catalysts revealed acceptable reusability and stability, and the degraded products were studied using the GC-MS technique with a proposed mechanism of degradation. The improvement in photodegradation of MB and Rh B dyes can be attributed to an increase in surface area, as well as the development of shape and optical characteristics.

Influence of the synthesis route on optical and luminescence properties of glass-ceramic doped with europium ions

The production of transparent glass-ceramic materials often faces challenges, such as inhomogeneities, inclusions, uncontrolled crystallization and other defects that make glass ceramics unsuitable for fiber optics, for example. At the same time, the chosen chemical composition is valuable for its unique properties. The present study investigated the effect of different methods of synthesizing glass-ceramic silica-germanium-antimony matrices on their transmittance optimization and luminescence properties where the conventional melt-quenching route is insufficient in terms of the transparency and homogeneity of the material obtained. The effect of heat treatment on the studied properties was also considered. Full Text: PDF References G.A. Khater, E.M. Safwat, J. Kang, Y. Yue, A.G.A. Khater, "Some Types of Glass-Ceramic Materials and their Applications", Int. J. Res. Stud. Sci. 7(3), 1 (2020). DirectLink J. Deubener, M. Allix, M.J. Davis, A. Duran, T. Höche, T. Honma, et al., "Updated definition of glass-ceramics", J. Non-Crystalline Solids 501, 3 (2018). CrossRef W. Blanc, Y. Gyu Choi, X. Zhang, M. Nalin, K.A. Richardson, G.C. Righini, et al., "The past, present and future of photonic glasses: A review in homage to the United Nations International Year of glass 2022", Progr. Mat. Sci. 134, 101084 (2023). CrossRef P. Golonko, M. Kochanowicz, P. Miluski, M. Kuwik, J. Pisarska, W. Pisarski, J. Dorosz, M. Leśniak, D. Dorosz, A. Basa, J. Żmojda, "Glass-ceramic optical fibers with controlled crystallization of core doped with europium ions", Ceram. Int. S0272884224002955 (2024). CrossRef J. Zmojda, M. Kochanowicz, P. Miluski, A. Baranowska, A. Basa, R. Jadach, M. Sitarz, D. Dorosz, "The influence of Ag content and annealing time on structural and optical properties of SGS antimony-germanate glass doped with Er3+ ions", J. Mol. Struct. 1160, 428 (2018). CrossRef X. Liu, J. Zhou, S. Zhou, Y. Yue, J. Qiu, "Transparent glass-ceramics functionalized by dispersed crystals", Progr. Mat. Sci. 97, 38 (2018). CrossRef T.N.L. Tran, A. Chiasera, A. Lukowiak, M. Ferrari, "Eu3+ as a Powerful Structural and Spectroscopic Tool for Glass Photonics", Materials 15, 1847 (2022). CrossRef Z. Li, L. Tan, C. Chen, D. Zhou, L.R. Jensen, J. Ren, Y. Zhang, J. Qiu, Y. Yue, "The effect of melt-homogenization and heat-treatment on the optical properties of the rare earth doped oxyfluoride glass-ceramics", J. Non-Cryst. Solids 593, 121773 (2022). CrossRef D. Dorosz, M. Kochanowicz, R. Valiente, A. Diego-Rucabado, F. Rodríguez, N. Siñeriz-Niembro, et al., "Pr3+-doped YPO4 nanocrystal embedded into an optical fiber", Sci Rep. 14, 7404 (2024). CrossRef

Zinc oxide (ZnO) Enhanced with Silver (Ag) is Used to Improve the Photocatalytic Degradation of Phenol in Aqueous Solutions

Silver-modified zinc oxide (Ag/ZnO) photocatalysts were synthesized and characterized to evaluate their efficiency in degrading phenol under UV irradiation. X-ray fluorescence, surface area analysis, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and UV-visible reflectance spectroscopy confirmed successful deposition of metallic silver (Ag0) nanoparticles on the ZnO surface. The abundance of silver particles correlated directly with Ag concentration. Surface plasmon resonance bands indicated silver nanoparticle formation. Photocatalytic testing showed increased phenol degradation with Ag/ZnO versus pure ZnO, with 0.88 wt% Ag being optimal. Further experiments found 50 mg/L initial phenol and 0.15 g/L photocatalyst dosage optimized performance. Finally, almost complete elimination of phenol from drinking wastewater occurred after 180 minutes with the enhanced Ag/ZnO photocatalyst under UV irradiation.

Mechanical characterization of nanocrystalline Cu-Ag alloys subjected to shear deformation

ABSTRACT This study investigates the mechanical behaviour of nanocrystalline Cu-Ag alloys using molecular dynamics simulations combined with detailed analyses of dislocation densities, atomic populations, and deformation characteristics. Shear tests were conducted across three different atomic compositions at temperatures ranging from 10 K to 500 K. The influence of temperature and Ag impurities on the mechanical properties of nanocrystalline Cu is explored. Elevated temperatures are found to promote plastic deformation by increasing atomic mobility, resulting in reduced dislocation densities and flow stresses. Increasing Ag content correlates with lower dislocation densities, highlighting enhanced plastic activity between grain and grain boundaries. Structural population analysis underscores the significant impact of Ag species on the mechanical response of nanocrystalline Cu. Further investigations are warranted to explore additional deformation mechanisms. These findings contribute to a deeper understanding of nanocrystalline Cu-Ag alloys, informing the design of novel materials with tailored mechanical properties.

Organic matter is a predominant control on total mercury concentration of near-surface lake sediments across a boreal to low Arctic tundra transect in northern Canada

Mercury (Hg) is a bioavailable and toxic element with concentrations that are persistently high or rising in some Arctic and subarctic lakes despite reduced atmospheric emissions in North America. This is due to rising Hg emissions to the atmosphere outside of North America, enhanced sequestration of Hg to sediments by climate-mediated increases in primary production, and ongoing release of Hg from terrestrial reservoirs. To evaluate the influence of organic matter and other parameters on Hg accumulation in northern lakes, near-surface sediments were sampled from 60 lakes across a boreal to shrub tundra gradient in the central Northwest Territories, Canada. The organic matter of the lake sediments, assessed using programmed pyrolysis and petrology, is composed of a mixture of terrestrial, aquatic, and inert organic matter. The proportion of algal-derived organic matter is higher in sediments of lakes below treeline relative to shrub tundra sites. Total sedimentary Hg concentration is correlated to all organic matter constituents but is unrelated to latitude or lake position below or above treeline. The concentrations of Ag, Ca, P, S, U, Ti, Y, Cd, and Zn are also strong predictors of total sedimentary Hg concentration, indicating input from a common geogenic source and/or common sequestration pathways associated with organic matter. Catchment area is a strong negative predictor of total sedimentary Hg concentration, particularly in lakes above treeline, possibly due to retention capacity of Hg and other elements in local sinks. This research highlights the complexity of controls on Hg sequestration in sediment and shows that while organic matter is a strong predictor of total sedimentary Hg concentration on a landscape scale and across extreme gradients in climate and associated vegetation and permafrost, other factors such as catchment area and sources from mineralized bedrock are also important.

Modulating Schottky barriers and active sites of Ag-Ni bi-metallic cluster on mesoporous carbon nitride for enhanced photocatalytic hydrogen evolution

The advancement of photocatalysis relies on the development of novel hetero-structured materials with unique architectures. In this study, we successfully synthesized a hetero-structured g-C3N4 (GCN) material with a distinctive surface-interface modification. To further enhance its photocatalytic performance, we optimized the Ag and Ni concentration to maximize the visible light absorption and catalytic active sites for hydrogen evolution reactions. By using systematic physicochemical characterizations and density functional theory (DFT) calculations, we elucidated the pivotal role of graphitic carbon nitride (g-C3N4) in facilitating the formation of an efficient charge transfer channel and promoting the effective generation and separation of photo-generated carriers. From the DFT calculations, we also demonstrated that the Ag and Ni nanoparticles provide more efficient visible light absorption and active sites than Ni nanoparticles for water splitting and hydrogen evolution and In-situ TEM exploration. Furthermore, the hetero microstructure consisting of thin g-C3N4 nano scrolls has a crucial role in shortening the migration distance of the carriers, effectively suppressing carrier recombination. Consequently, these extraordinary characteristics resulted in a superior solar light-driven photocatalytic H2 evolution rate of 2507 μmol.h-1.g−1, surpassing the rate achieved by g-C3N4 heterostructures by a remarkable 18.6-folds. Moreover, the apparent quantum efficiency of this hetero-structured material reached an exceptional value of 1.6 % under a 1.5 G air mass filter.

Study on the preparation of bimetallic silver-copper nanoparticles by electron beam irradiation

Silver and copper nanoparticles are well-known as good antimicrobial agents. In this study, we reported the preparation and characterization of bimetallic silver-copper nanoparticles (Ag-CuNPs) prepared by the electron beam (EB) irradiation method. Chitosan (CTS) was used as a stabilizer agent. The obtained Ag-CuNPs were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and UV-Vis spectrophotometry. The influence of the different concentrations in the range of 100–1,000 ppm of Ag+ and Cu2+ ions at the mass ratio of [Ag+]:[Cu2+] = 1/1 on the particle size and particle size distribution of the Ag-CuNPs was investigated. The TEM results showed that the average size of the Ag-CuNPs was 11.02–13.73 nm when the total concentration of Ag+ and Cu2+ ions was 250 – 1,000 ppm, respectively. The EB-irradiation method can be applied in the production of Ag-CuNPs on a large scale.

Simultaneous improvement in mechanical properties, corrosion resistance and antibacterial properties of Ti-Ag sintered alloy with gradient nanostructure

Bioinert titanium (Ti) with antibacterial properties is crucial for bone implantations. Alloying Ag can endow Ti with antibacterial properties, while the mechanical, corrosion and antibacterial properties of Ti-Ag alloys are not satisfactorily balanced. In this work, Ti-x wt%Ag alloys (x=0.5, 1 and 3) were sintered by spark plasma sintering and then subjected to a surface mechanical rolling treatment (SMRT). The Ti-Ag alloys are composed of Ti, Ti-Ag and Ti2Ag phases. After SMRT, a gradient nanostructured (GNS) layer formed on the Ti-Ag surface, the mean grain size is ∼ 6 nm at the top surface and increases gradually with depth. The GNS layer endows Ti-Ag alloys with better wettability, higher nano-roughness and compressive residual stress. Incorporating limited Ag (≤1 wt%) in Ti can effectively enhance its mechanical (surface hardness, wear resistance and compressive strength) and anti-corrosion properties, and they can be further improved by forming a GNS layer. The antibacterial efficiency of Ti-Ag is positively proportional to Ag content, and they are significantly enhanced after surface nanocrystallization. The bacteriostatic mechanism is the synergistic interaction between leach Ag+ and nano Ag-containing phases of GNS Ti-Ag alloy. Both Ti-Ag and GNS Ti-Ag alloys possess good cytocompatibility, the GNS layer has the potential to encourage early differentiation of osteoblasts. The GNS Ti-Ag alloy with 1 wt% Ag has excellent comprehensive properties, which shows larger potential in orthopedic applications.

Impact of Silver Incorporation and Flash-Lamp-Annealing on the Photocatalytic Response of Sputtered ZnO Films.

Thin films of silver-doped zinc oxide (SZO) were deposited at room temperature using a DC reactive magnetron co-sputtering technique using two independent Zn and Ag targets. The crystallographic structure, chemical composition and surface morphology of SZO films with different silver concentrations were correlated with the photocatalytic (PC) properties. The crystallization of the SZO films was made using millisecond range flash-lamp-annealing (FLA) treatments. FLA induces significant structural ordering of the wurtzite structure and an in-depth redistribution of silver, resulting in the formation of silver agglomerates. The wurtzite ZnO structure is observed for silver contents below 10 at.% where Ag is partially incorporated into the oxide matrix, inducing a decrease in the optical band-gap. Regardless of the silver content, all the as-grown SZO films do not exhibit any significant PC activity. The best PC response is achieved for samples with a relatively low Ag content (2-5 at.%) after FLA treatment. The enhanced PC activity of SZO upon FLA can be attributed to structural ordering and the effective band-gap narrowing through the combination of silver doping and the plasmonic effect caused by the formation of Ag clusters.

Synergistic enhancement of plasmon induced photocatalytic and photoelectrochemical performance on ZnWO4/Ag2O@Ag hybrid-heterostructures

A novel hybrid photocatalyst, ZnWO4/Ag2O@Ag heterostructure was synthesized using a simple one-pot microwave treatment with varying concentrations of silver. Physico-chemical characterization was performed to elucidate the synthesized nanohybrids' properties. The photocatalytic activity of both pristine and heterostructure samples was evaluated through the degradation of cationic MB dye. Among the varied Ag concentrations, the 9 % Ag-doped ZnWO4/Ag2O heterostructure exhibited superior degradation performance, with a degradation rate of 93 % achieved within 45 min, surpassing both other Ag concentrations (89 % (90 min) for 1 % Ag, 87 % (80 min) for 3 % Ag, 90 % (80 min) for 5 % Ag and 91 % (45 min) for 7 % Ag) and pristine ZnWO4 (91 % (90 min)) samples. This catalytic enhancement can be attributed to the formation of heterostructures, plasmon-induced absorption enhancement within specific wavelength ranges, and reduced charge recombination rates. UV–visible studies revealed Ag nanoparticles of various sizes in the heterostructures, supported by surface plasmon resonance (SPR) peaks at 480 and 550 nm, respectively. Trapping experiments indicated that •OH and •O2− were the active species in MB reduction for pure and heterostructure samples. Furthermore, the hybrid heterostructure samples exhibited high stability and reusability in photocatalytic degradation. These findings suggest that the ZnWO4/Ag2O heterostructure photocatalysts are promising candidates for environmental remediation applications.