Spherical Silver Research Articles

Effect of silver morphology on rheology and photopolymerization characteristics of Silver-Hydroxyapatite slurry for Vat Photopolymerization-based 3D printing process

The present work deals with the processing of HA-silver photocurable slurry to make composites using the Vat-photopolymerization process. Slurries with increasing amount of silver addition in the HA-Ag (0, 5, 10, 15%) slurry have been prepared using monomers with photo-initiators and printed successfully. Silver powder used in this study is in the form of flakes and spheres. A shear thinning behaviour of all the compositions of the slurries has been observed which is essential to fabricate defect-free parts. With increase in silver addition to 15 wt%, the viscosity decreased by around 60 % however curing depth was compromised. From SEM micrographs it was observed that HA with silver flakes showed better sintering with sintering density of 95% compared to only HA and HA with spherical silver samples.

Bio-synthesized AGS@AgNPs for wound healing, antioxidant support, antibacterial defense, and anticancer intervention

Slow wound healing and wound infections are significant challenges for burn patients. Biosynthesis of nanoparticles (NPs) using plant extracts offers a rapid, facile, and safe method for producing biocompatible NPs. In this study, Anethum graveolens seed (AGS) extract served as a masking and reducing agent for the synthesis of silver nanoparticles (AGS@AgNPs). Initially, the parameters influencing AGS@AgNPs synthesis, including silver nitrate concentration, reaction time, temperature, and pH, were optimized. Subsequently, AGS@AgNPs structural and biological characteristics were evaluated. Observation of the surface plasmon resonance (SPR) of the AGS@AgNPs at approximately 420 nm, accompanied by a color change of the suspension to dark brown, confirmed AGS@AgNPs synthesis. Analysis via X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS), zeta potential, and transmission electron microscopy (TEM) confirmed the production of pure, homogeneous, spherical, and stable silver NPs with sizes ranging from 20 to 40 nm using Anethum graveolens extract. Antibacterial assays revealed significant activity against both Gram-positive and Gram-negative bacterial strains. Antioxidant assessments demonstrated that AGS@AgNPs at a concentration of 250 μg/ml exhibited 92% inhibition of DPPH free radicals and in FRAP test, A. graveolens seed extract and AGS@AgNPs reduced Fe3+ ions to Fe2+ by 48.7% and 73.1%, respectively. Investigation of anticancer properties against the lung cancer cell line (A-549) revealed an IC50 value of 242 μg/ml. The results of the flow cytometry test and lactate dehydrogenase (LDH) assay demonstrated the death of cancer cells. Moreover, wound healing assays demonstrated a significant acceleration in burn wound closure rates in rats on days 3, 7, and 14 following treatments with AGS@AgNPs. Overall, these findings highlight the favorable biological activities of AGS@AgNPs, suggesting their potential utility in nanomedicine applications.

Synthesis of uniform spherical silver powder without dispersants in a confined impinging-jet reactor

Sliver powder is the most common and extensively utilized precious metal powder in electronics, primarily for electronic paste. Herein, micron-sized spherical silver powder was synthesized via a liquid phase reduction method employing silver nitrate as the source of silver and ascorbic acid as the reducing agent in a confined impinging jet reactor (CIJR). The impact of the molar ratio between silver nitrate and ascorbic acid, the flow rate, and the temperature on the particle size of silver powder was investigated. The optimal process conditions for silver powder are as follows: maintain a molar ratio of 1:1 and control the feeding rate at 10 ml/min while operating at 50 ° C. The confined impinging jet reactor offers enhanced control over reaction conditions during the synthesis of silver powder, surpassing the capabilities of traditional batch reactors. The aforementioned optimized methodology was employed to successfully synthesize uniform and spherical silver powder (with an aspect ratio approaching 1) in the low Reynolds number jet, resulting in an average particle size of d50 = 0.83 μm and a standard deviation of 0.07, without the addition of dispersant. The synthesis method presented here improves the performance of silver powder, simplifies the production process, reduces energy consumption, and minimizes waste generation. These advances yield significant environmental and economic benefits. In the future, with the continuous development and optimization of microreactor technology, this synthesis method is anticipated to play a more prominent role in the commercial-scale production and application of micrometer-sized silver powder.

Fabrication, catalytic activity, metal sensing ability and electrochemical evaluation of nano silver particles for supercapacitor applications

In this work, stable, spherical silver nanoparticles (MAgNp) were prepared via a green synthesis method using flowers of Myristica fragrans (nutmeg). This flower is abundant in phytochemicals such as saponins that can be utilized as reductants to produce silver nanoparticles. The synthesized nanoparticles were examined using a variety of physico-chemical methods, including transmission electron microscopy (TEM), Dynamic light scattering (DLS), elemental dispersive X-ray spectroscopy (EDX), powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and UV–VIS spectrometer. EDX study confirmed the crystalline and face-centered cubic (FCC) structure of AgNP. The majority of particles are present with a higher percentage intensity at an average size of 58.77 nm as revealed in the TEM image, PDI was found to be 0.055. MAgNPs demonstrated perfect activity in the catalytic degradation of methylene blue dye (88 %) and para-nitrophenol (98 %), both anthropogenic pollutants. These nanoparticles were further used as plasmonic sensors to detect heavy metals like Fe(II) and Hg(II) in an aqueous solution. The minimum detection limit was found to be 0.2 mM for Hg(II) and 10 μM for Fe(II) with good linearity. The electrochemical properties of MAgNPs were studied using a carbon supercapacitor electrode coated with MAgNPs. Results from cyclic voltammetry were also determined, and they showed a high specific capacitance of 41 F/gm at 5 mV/s scan rate.

SERS Platform for Integrated Enrichment, Isolation, and Identification of Multiple Respiratory Viruses in a Single Assay Using 3D Stereoscopic SERS Tags and Flocked Swabs.

Influenza (flu) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) exhibit similar clinical symptoms, complicating the diagnosis and clinical management of these critical respiratory infections. Thus, there is an urgent need for rapid on-site detection technologies that can simultaneously detect SARS-CoV-2 and influenza A viruses. Here, we have developed the first platform that combines in situ sampling with immune swabs and multichannel surface-enhanced Raman spectroscopy (SERS) for simultaneous screening of these two respiratory viruses in a single assay. A seed-mediated growth method was used to assemble a number of silver spheres on the surface of Fe3O4@SiO2 spheres, which not only creates extensive Raman hotspots but also provides numerous sites for Raman signaling molecules, enhancing the sensing sensitivity. Integrating two specific Raman signaling molecules into the nanospheres allows for the parallel detection of both viruses, improving the efficiency of SERS signal read-out. Rapid quantitative screening of both SARS-CoV-2 and H1N1 is achievable within 15 min, with detection limits of 7.76, and 8.13 pg·mL-1 for their respective target proteins. The platform demonstrated excellent performance in testing and analyzing 98 clinical samples (SARS-CoV-2:50; influenza A:48), achieving sensitivities of 88.00, and 95.83% for SARS-CoV-2 and influenza A, respectively. Pearson's correlation analysis revealed a significant correlation with the clinical CT values (P < 0.0001), underscoring the great potential of this platform for the early, rapid, and simultaneous diagnostic discrimination of multiple pathogens.

Novel spherical and homogeneous Alstonia Scholaris silver nanoparticles for dual applications: Detection of ultra-trace amounts of Cr(III) ions and MB discoloration sustained by 3-input AND gate

This study unveils an effective method for detecting Cr(III) and MB dye discoloration using biosynthesized silver nanoparticles obtained from leaves of Alstonia Scholaris (AS-AgNPs). HR-TEM images showed that the mean diameter of AS-AgNPs increased from 14.68 to 37.05 nm after the interaction with Cr(III) ions. The AS-AgNPs show an impressive detection limit of 2.1 nM for Cr(III) and demonstrate high efficacy in MB discoloration of 91.27% in 12 min. The discoloration reaction fitted pseudo-first-order kinetics with the R2 value of 0.9634. When comparing the kinetics of MB discoloration by NaBH4 alone, and addition of AS-AgNPs to NaBH4 resulted in a 102 fold decrease in t1/2 and a 102 fold increase in k values. This is the first report to use spherical AS-AgNPs for dual applications, supported by 3-Input AND gate logic, and also highlights AS-AgNPs' potential application for real sample analysis.

Biosynthesized Self-Assembled Silver Spheres and Their Electrochemical Characterization

Biosynthesized Self-Assembled Silver Spheres and Their Electrochemical Characterization

Real-time cationic sensing using plasmonic fiber optic sensor based phosphoryl-carrageenan

We report Fiber Optic-Localized Surface Plasmon Resonance (FO-LSPR) spectroscopy sensors comprising a coating of spherical silver nanoparticles (AgNPs) embedded in phosphoryl-carrageenan. This is a novel report on modified carrageenan namely phosphoryl-carrageenan as sensing materials for cations specifically ammonium ions (NH4+). The morphology of carrageenan and phosphoryl-carrageenan coatings on the fiber optic probe was uneven and wavelike topography, indicating the successful coating on the fiber optic probe surface. The FO-LSPR showed a distinct dip in reflectivity in the region of 370–400 nm due to the resonance frequency of spherical AgNPs. The response and recovery times of FO-LSPR sensors for 1 ppm NH4+ and deionized water were <20 s and ∼1.2 minutes, respectively, with five times stable repeatability. The sensitivity of the FO-LSPR phosphoryl-carrageenan was 3.441 nm/ppm. Equally, the limits of detection and quantitation of fiber optic FO-LSPR were 0.336 and 1.018 ppm, respectively. Meanwhile, the dynamic range of the FO-LSPR was 0.3 – 2.0 ppm. The proposed sensor demonstrated strong selectivity towards NH4+ over common cationic interferents. Furthermore, the reported FO-LPSR sensor offered a comparable measurement performance to current methods, while being low cost and portable, and allowing in-situ real-time monitoring of cation ammonium. Thus, reported FO-LPSR sensors are highly promising for water monitoring applications.

Light-mediated biosynthesis of size-tuned silver nanoparticles using Saccharomyces cerevisiae extract

Bio-based production of silver nanoparticles represents a sustainable alternative to commercially applied physicochemical manufacturing approaches and provides qualitatively highly valuable nanomaterials due to their narrow size dispersity, high stability and biocompatibility with broad application potentials. The intrinsic features of nanoparticles depend on size and shape, whereby the controlled synthesis is a challenging necessity. In the present study, the biosynthesis of size-tuned silver nanoparticles based on cell-free extracts of Saccharomyces cerevisiae DSM 1333 was investigated. Single parameter optimization strategies in phases of cultivation, extraction, and synthesis were performed to modify the nanoparticle scale and yield. Visible light was exploited as a tool in nanoparticle production. The influence of white light on the biosynthesis of silver nanoparticles was determined by using novel LED systems with the exposition of varying irradiation intensities and simultaneous performance of control experiments in the dark. Characterization of the resulting nanomaterials by spectrophotometric analysis, dynamic light scattering, scanning electron microscopy, and energy dispersive X-ray spectroscopy, revealed spherical silver nanoparticles with controlled, light-mediated size shifts in markedly increased quantities. Matching of irradiated and non-irradiated reaction mixtures mirrored the enormous functionality of photon input and the high sensitivity of the biosynthesis process. The silver nanoparticle yields increased by more than 90% with irradiation at 1.0±0.2mWcm-2\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$1.0 \\pm 0.2\ ext{ mW }{\ ext{cm}}^{-2}$$\\end{document} and the reduction of particle dimensions was achieved with significant shifts of size-specific absorption maxima from 440 to 410 nm, corresponding to particle sizes of 130 nm and 100 nm, respectively. White light emerged as an excellent tool for nano-manufacturing with advantageous effects for modulating unique particle properties.Graphical abstract

Effect of Spherical Silver Particles Size of the Catalyst Bed on Hydrogen Peroxide Monopropellant Thruster Performance

Effect of Spherical Silver Particles Size of the Catalyst Bed on Hydrogen Peroxide Monopropellant Thruster Performance

Optimizing Silver Paste Conductivity with Controlled Convection for Nanowrinkle Growth.

Conductive silver paste plays a crucial role as an interconnecting material between electrodes and circuits in electronic circuits and solar cells. The quality of the silver paste is greatly influenced by the preparation of the conductive-phase silver powder and the sintering process. This study investigated the impact of fluid dynamics on the preparation of silver powder. Combined with X-ray diffractometer characterization and molecular dynamics simulation, the formation mechanism of wrinkled silver powder was explained. The wrinkled silver powder replaced the traditional smooth spherical silver powder, and the point contact between the smooth silver powder turned into a line and surface contact. After mixing and sintering with the micrometer flake silver powder, the electrical conductivity and sintering morphology of the silver paste were improved. Compared with the silver content of conventional silver paste (≥75 wt %), the silver paste of (9.23 ± 0.68) × 10-6 Ω cm can be prepared by curing at 250 °C for 45 min when wrinkled powder/flake powder = 1:1 and silver paste content was only 66.7%. This research work provides a new idea for the morphology control of submicrometer silver powder, which has important applications in the field of low-temperature silver paste for new N-type batteries.

Biofabrication of Centella asiatica mediated metal (Silver and Iron) nanoparticles and their enhanced antimicrobial, anticancer activity in retinoblastoma Y79 cancer cells

In recent years, metallic nanoparticles have played a significant role in nanotechnology and bio fabrication, being considered an alternative to antibiotics due to their feasibility for use in both bacterial detection and infection prevention. Moreover, recent studies have demonstrated the green process of developing nanoparticles with anticancer activity against many human cancer cell lines. In the current investigation, the biogenic synthesis of silver and iron nanoparticles using the aqueous leaf extract of Centella asiatica was performed. The leaf extracts underwent characterization for antioxidant activity, TLC analysis, phytochemical analysis, and GC-MS analysis of Centella asiatica. The leaf extracts revealed the antioxidant potential of the phytoconstituents, namely phenolic and flavonoid contents, responsible for the anticancer activity. The synthesized silver and iron nanoparticles were analysed using various techniques, including UV-Vis absorption spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy with energy-dispersive spectroscopy, and transmission electron microscopy. Confirmation of silver and iron nanoparticle formation was achieved through UV-Vis absorption spectra, showing absorption peaks at 362 nm and 342 nm, respectively. Fourier transform infrared spectroscopy analysis confirmed the biological moieties involved in synthesis and stability. X-ray diffraction (XRD) analysis verified the crystallinity of the nanomaterials, while scanning electron microscopy depicted spherical shapes for silver nanoparticles and similarly round shapes for iron nanoparticles. EDS analysis revealed 87.12 % silver and 40.12 % iron content in the respective nanoparticles. TEM imaging displayed predominantly spherical silver nanoparticles, sized at 50 nm. The antimicrobial efficacy of the biosynthesized silver and iron nanoparticles was evaluated using the well diffusion method, along with the determination of the minimum inhibitory concentration. Results indicated moderate effectiveness of silver nanoparticles against Escherichia coli (7±0.036) and Aspergillus niger (5±0.034) compared to iron nanoparticles. The minimum inhibitory concentrations against Staphylococcus aureus were 46.51–86.74 % for silver nanoparticles and 42.79–77.44 % for iron nanoparticles. The anticancer effect was evaluated using human retinoblastoma (Y79) cell lines. The cytotoxicity study using the MTT assay revealed that Centella asiatica-mediated silver nanoparticles exhibited significant cytotoxicity to human retinoblastoma cells, with a low IC50 value of 49.56 μg/ml. Based on the results, it is feasible to infer that biofabricated nanoparticles could potentially serve as antibacterial and antifungal compounds. Furthermore, the synthesized silver nanoparticles, followed by iron nanoparticles, showed high effectiveness against human retinoblastoma cancer cells, indicating potential for future drug discovery to inhibit retinoblastoma cancer for biomedical applications.

Bioinspired synthesis of multifunctional, highly stable polymeric templated silver-silica colloids as catalytic and antibacterial coatings for paper

In this paper, a simple, bottom up, bioinspired technique is proposed for the synthesis of highly stable colloids of silica supported spherical silver nanoparticles (SiO2@Ag) that act as efficient catalytic and antimicrobial coatings for an organic substrate, filter paper. The core – shell structure and the highly branched dendritic polymer, poly(ethylene)imine, enabled the precise control of growth rate and morphology of silica and silver nanoparticles. The polymer also enabled the deposition of these nanoparticles onto an organic substrate, filter paper, through immersion by modifying its surface. The catalytic and antibacterial properties of these samples were assessed. The results obtained from this analysis showed a complete degradation of an aqueous pollutant, 4-nitrophenol, for 6 successive catalytic cycles without intermediate purification steps. Furthermore, the polymeric silica-silver suspension proved to express antibacterial activity against both Gram-positive and Gram-negative bacteria (Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa). The antibacterial properties were evaluated according to the disk diffusion method, whereas the Minimum Inhibitory Concentration was also determined. The samples were examined by Scanning Electron Microscopy, Transmission Electron Microscopy, X-ray diffraction analysis, z-potential analysis, Fourier Transform Infrared Spectroscopy and Ultraviolet-visible Spectroscopy.

Phytofabrication of silver nanoparticles from Illicium verum fruit extract and its role in Cr+6 removal: a comparative analysis

ABSTRACT Herein, using Illicium verum (IV) aqueous fruit extract, spherical shape silver nanoparticles (IV-AgNPs) of 40 nm average size with typical SPR at 422 nm were synthesised through the one-pot chemical reduction method. In the presence of Cr+6, IV-AgNPs rapidly changed from yellow to pink colour, with immediate SPR quench at 422 nm and new peak appearance at 510 nm, suggesting carboxylate groups involvement in AgNPs synthesis and Cr+6 interaction, respectively. Clusters were formed in Cr+6 presence; as a result, IV-AgNPs’ zeta potentials changed from −24.1 to 14 mV. Moreover, with the lowest limit of detection (22.1 nM), IV-AgNPs displayed higher potential for Cr+6 adsorption in aqueous medium. The Langmuir isotherm predicts monolayer adsorption on a homogeneous surface of both adsorbents via chemisorption kinetics with adsorption capacity of 1511.65 and 720.35 mg/g for IV-AgNPs and IV fruit extract, respectively. Calculated thermodynamic values of -∆G°, +∆H°, and +∆S° indicate spontaneity, randomness, and endothermicity of the adsorbate system(s). Akaike information criterion ranking alignment and kinetics equilibrium for adsorbents showed that the Elovich plot and intra-particle diffusion produced the best output in comparison to other models. These findings indicate adsorption dynamics are controllable for both adsorbents, but the size-dependent properties of IV-AgNPs significantly improve interaction efficiency for Cr+6 adsorption.

Localized surface plasmon resonance (LSPR) excitation on single silver nanoring with nanoscale surface roughness

With the expansion of the application of high-sensitivity Surface-enhanced Raman scattering (SERS) technique, micro SERS-active substrates with rich optical properties and high-level functions are desired. In this study, silver nanorings with nanoscale surface roughness were fabricated as a new type of enclosed quasi-2D micro-SERS-active substrate. Highly-crystalline spherical and hemispherical silver nanoprotrusions were densely and uniformly distributed over the entire surface of the nanorings. The SERS signals were significantly enhanced on the roughened silver nanorings which were mainly derived from the maximal localized surface plasmon resonance (LSPR) points at the junctions between adjacent coupled nanoprotrusions on the roughened nanorings. The mapping image shows a uniform and intense LSPR enhancement over the nanorings, owing to the uniform and dense distribution of silver nanoprotrusions and the resulting uniform distribution of maximal LSPR points on the roughened nanorings. The dark-field spectra further indicated that the single roughened silver nanoring had significant LSPR enhancement, a wide LSPR frequency-range response, and adaptability for SERS enhancement. Notably, both the measured and simulated results demonstrate that the maximal LSPR enhancement at the junctions between the nanoprotrusions, which are distributed on the inner surface of the silver nanoring, is higher than that on the outer surface because of the plasmon-focusing effect of the enclosed silver nanoring, which leads to the lateral asymmetrical distribution of LSPR intensity, indicating more LSPR and SERS features. These results indicate that single roughened silver nanorings exhibit excellent performance as a new type of enclosed quasi-2D silver nanoring micro-SERS-active substrate, microzone LSPR catalysis, and micro/nanodevices.

Fröhlich resonance splitting in hybrid GaN nanowire-Ag nanoparticle structures

Plasmonic nanoparticles (NPs) have attracted significant attention due to their unique optical properties and broad optoelectronic and photonic applications. We investigate modifications of emission in hybrid structures formed by 60 nm silver NPs and GaN planar nanowires (NWs). Bare GaN NWs exhibit photoluminescence (PL) spectra dominated by broad bands peaking at ∼3.44 eV and ∼3.33 eV, attributed to basal plane stacking faults. In hybrids, two new narrow PL lines appear at 3.36 and 3.31 eV, resulting in PL enhancement at these energies. While the 3.36 eV line in hybrid structures can be explained using the Fröhlich resonance approximation based on the electric dipole concept, the appearance of two features at 3.36 and 3.31 eV indicates the splitting of resonance lines. This phenomenon is explained in framework of theoretical model based on the interaction of the dipole with its charge image, taking into account the quadrupole moment of the silver sphere and the quadrupole field of the charge image. A good agreement is obtained between the calculated Fröhlich resonance frequencies and the experimental PL lines in hybrid structures.

Asphaltene-derived nanocomposites for the removal of emerging pollutants and its antimicrobial effects: batch and continuous column studies.

Emerging contaminants are diverse ecotoxic materials requiring unique treatment for removal. Asphaltenes are environmentally hazardous carbon-rich solid waste product of the petroleum industry. In the current work, asphaltene-derived activated carbon (AC) was loaded with silver (Ag/AC) and used to remove amoxicillin (AMX) and tetracycline (TC) from aqueous phase. The prepared Ag/AC was characterised using FESEM, FTIR, XRD and surface area analysis. The FESEM micrographs confirmed the spherical silver nanoparticle-laden porous AC, and the BET surface area was found to be 213 m2/g. Batch adsorption studies were performed, and the equilibrium data were fit into adsorption isotherm and kinetic models. The Ag/AC exhibited superior monolayer adsorption capacity of 1012mg/g and 770mg/g for AMX and TC, respectively. The continuous column studies were also performed to evaluate the breakthrough parameters. Furthermore, the antimicrobial activity of the adsorbent was evaluated using zone of inhibition studies. Ag/AC was found to have an 8-mm-diameter zone of microbial inhibition. The obtained results showed that Ag/AC was a promising material for the removal of antibiotics and inhibition of resistance-developed mutated microbes in effluent water.

Chemistry of plant extracts directs the silver nanostructures’ crystal structure into hexagonally close-packed: a comparative study using elecampane and blueberry extracts

In this study, silver nanostructures (AgNSs) were obtained using aqueous extracts of elecampane ( Inula viscosa) and blueberry ( Vaccinium arctostaphylos L.). The synthesized AgNSs were characterized using UV–visible spectrophotometers, Fourier-transformed infrared spectroscopy, scanning electron microscopy-energy dispersive X-ray analysis, high-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy. The optimization studies revealed that pH and the extract/AgNO3 ratio played significant roles in the morphology and size of the AgNSs, while temperature did not show any significant role. Both the blueberry and elecampane extracts resulted in a mixture of spherical and aspherical silver nanoparticles (AgNPs). In contrast, utilization of a relatively high extract/AgNO3 ratio accompanied by an extended incubation period (i.e., 10 days) caused the formation of larger spherical (e.g., up to micron-sized) and large 1D AgNPs for the blueberry and elecampane extracts, respectively. The major difference related to the crystal structures was obtained, as the blueberry extracts resulted in face-centric cubic crystals, and the elecampane extracts allowed the formation of hexagonally close-packed (hcp) crystalline structures. The AgNPs were tested for their antibacterial activities using gram (−) and gram (+) bacterial species, where the elecampane-synthesized AgNPs possessed higher antibacterial activity that can be attributed to the hcp crystalline structure of the AgNPs.

High-Quality Spherical Silver Alloy Powder for Laser Powder Bed Fusion Using Plasma Rotating Electrode Process.

The plasma rotating electrode process (PREP) is an ideal method for the preparation of metal powders such as nickel-based, titanium-based, and iron-based alloys due to its low material loss and good degree of sphericity. However, the preparation of silver alloy powder by PREP remains challenging. The low hardness of the mould casting silver alloy leads to the bending of the electrode rod when subjected to high-speed rotation during PREP. The mould casting silver electrode rod can only be used in low-speed rotation, which has a negative effect on particle refinement. This study employed continuous casting (CC) to improve the surface hardness of S800 Ag (30.30% higher than mould casting), which enables a high rotation speed of up to 37,000 revolutions per minute, and silver alloy powder with an average sphericity of 0.98 (5.56% higher than gas atomisation) and a sphericity ratio of 97.67% (36.28% higher than gas atomisation) has been successfully prepared. The dense S800 Ag was successfully fabricated by laser powder bed fusion (LPBF), which proved the feasibility of preparing high-quality powder by the "CC + PREP" method. The samples fabricated by LPBF have a Vickers hardness of up to 271.20 HV (3.66 times that of mould casting), leading to a notable enhancement in the strength of S800 Ag. In comparison to GA, the S800 Ag powder prepared by "CC + PREP" exhibits greater sphericity, a higher sphericity ratio and less satellite powder, which lays the foundation for dense LPBF S800 Ag fabrication.

Structure and optical characterization of chitosan-chitin/Ag nanocomposite thin films

Chitin and its derivatives are common natural polymers that are widely used in various technological fields. In recent years, considerable attention has been paid to the preparation of polymer nanocomposites based on metal nanoparticles (NPs). Chitin/chitosan-based composites due to high antibacterial activity are suitable for application in related food storage, textile industries. This paper presents an effective and simple method of obtaining chitosan-chitin copolymer/Ag nanocomposites with an extremely high content of metal nanoparticles. The structure and morphology of the synthesized nanocomposites were investigated using X-ray diffractometry, Fourier-transform infrared spectroscopy, electron microscopy, and their optical properties were studied using UV-VIS spectroscopy as well as spectral ellipsometry. It was ascertained that the resulting nanocomposite films are characterized by a uniform distribution of spherical silver nanoparticles, the sizes of which increase (from 55 up to 143 nm) with increasing the Ag+-ions concentration in the reaction mixtures. The optical absorption spectra of nanocomposites are characterized by the presence of an absorption maximum within the range 458…525 nm, which confirms the formation of Ag NPs. A monotonous increase in the values of the energies of optical transitions was observed in the process of increasing the average size of NPs