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WO3/Ag/TiO2 composite photoelectrodes were formed via the high-temperature calcination of a WO3 film, followed by the sputtering of a very thin silver film and deposition of an overlayer of commercial TiO2 nanoparticles. These synthetic photoanodes were characterized in view of the oxidation of a model organic compound glucose combined with the generation of hydrogen at a platinum cathode. During prolonged photoelectrolysis under simulated solar light, these photoanodes demonstrated high and stable photocurrents of ca. 4 mA cm−2 due, on one hand, to the occurrence of the so-called photocurrent doubling and, on the other hand, to the plasmonic effect of Ag nanoparticles. The post-photoelectrolysis analyses of the electrolyte demonstrated the formation of high-value final glucose photo-reforming products, principally gluconic acid, erythrose and formic acid. [ABSTRACT FROM AUTHOR]

Compared with other methods, the synthesis of metal nanoparticles by metal ion reduction using plant extracts as raw materials has the advantages of low cost, simple synthesis and environmental friendliness, and has garnered significant attention. To achieve this effect, in the form of green synthetic nano silver (AgNP), we mixed AgNO3 with attapulgite (ATP) and stirred it with clove plant extract at 80 °C. By changing the dosage of clove extract, a series of new samples were prepared by the same method. The shape and size of the synthesized silver nanoparticles on catalysts were visualized by transmission electron microscope (TEM) observations. The particle size of the optimally prepared nanoparticles ranges from 1 to 9 nm with spherical or roughly spherical forms. The inductively coupled plasma (ICP) results further demonstrated the reducing effect of clove extract on Ag. Increasing the amount of clove extract could promote the formation and loading of Ag on ATP. An outstanding catalytic performance of Ag/ATP under HCHO outperformed that synthesized without clove extract. With the addition of clove extract, the catalytic performance was enhanced by more than 40% compared to no addition. Among different nanoparticles, the catalytic oxidation activity of HCHO was best when the volume ratio of clove extract to Ag was 10:1. Therefore, the green synthesis of Ag/ATP catalysts using clove extracts can be considered an environmentally benign, superior approach. [ABSTRACT FROM AUTHOR]

This work demonstrates a completely wet-chemical procedure for the fabrication of a functional impedimetric humidity-sensing device on a titania (TiO2) surface. Optically transparent anatase TiO2 thin films were deposited on a glass substrate via dip-coating from a titanium tetraisopropoxide (TTIP)–acetylacetonate (AA)-based sol and surface-functionalized with a nickel oxide (NiOx) layer by ultraviolet (UV) photodeposition. Photodeposition was employed to form the interdigitated electrode pattern on the TiO2 surface as well through activation with a silver catalyst to promote electroless copper deposition. The relative humidity (RH) response of the pristine TiO2- and NiOx/TiO2-functionalized sensors was studied by impedance (Z) measurements in the 15%–90% RH range. It was found that while NiOx functionalization significantly dampens the RH–Z functional dependence, it improves its overall linearity and may successfully be employed for the purposeful design of titania-based sensing devices. [ABSTRACT FROM AUTHOR]

This document is a summary of a special issue of the journal Catalysts titled "Catalytic Epoxidation Reaction." The special issue focuses on the research efforts in catalyst and process intensification in the epoxidation of various substances, including gaseous molecules, molecules in multiphase, triglycerides, terpenes, and olefins. The special issue includes nine research articles and two reviews, covering topics such as kinetic modeling, catalyst preparation and characterization, and enzymatic catalysis. The articles provide insights into the epoxidation process and offer potential advancements for future research in this field. [Extracted from the article]

A series of Ag-modified manganese-mullite (SmMn2O5) catalysts with different Ag contents (1, 3, and 6 wt.%) were prepared via a citric acid sol–gel method for catalytic soot oxidation. The catalysts were characterized by powder X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), Raman spectroscopy, transmission electron microscopy (TEM), high-resolution transmission electron microscopy analysis (HRTEM), X-ray photoelectron spectroscopy (XPS), and H2 temperature-programmed reduction (H2-TPR). The soot oxidation activity of the mullite was significantly promoted by the addition of silver and affected by the loading amount of the metal. Herein, the influences of silver loading on the metal size distribution and its interactions with the mullite were studied. Based on these characterizations, a possible soot oxidation reaction mechanism was proposed for silver-modified SmMn2O5. [ABSTRACT FROM AUTHOR]

α-Ketoamide moieties, as privileged units, may represent a valuable option to develop compounds with favorable biological activities, such as low toxicity, promising PK and drug-like properties. An efficient silver-catalyzed decarboxylative acylation of α-oxocarboxylic acids with isocyanides was developed to derivatize the α-ketoamide functional group via a multicomponent reaction (MCR) cascade sequence in one pot. A series of α-ketoamides was synthesized with three components of isocyanides, aromatic α-oxocarboxylic acid analogues and water in moderate yields. Based on the research, the silver-catalyzed decarboxylative acylation confirmed that an oxygen atom of the amide moiety was derived from the water and air as a sole oxidant for the whole process. [ABSTRACT FROM AUTHOR]

The dwindling supply of fossil fuels has resulted in a search for an efficient alternative energy source. Hydrogen gas offers an abundant, clean-burning supply of energy that can be readily produced over time via the water-splitting reaction of sodium borohydride (NaBH4). This study explored the synthesis of a novel catalyst comprised of silver nanoparticles supported on fused carbon spheres (AgNP-FCS). This composite catalyst was then tested for its ability to optimize the hydrolysis reaction of NaBH4. The fused carbon spheres (FCS) were synthesized via a sustainable source, namely a dextrose solution. The synthesized AgNP-FCS catalyst was characterized using transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The average diameter of silver nanoparticles on the catalyst was found to be 30 nm with 3.7% loading. This catalyst was tested under various reaction conditions, including temperatures, doses of NaBH4, and solution pHs. The activation energy of the reaction as catalyzed by AgNP-FCS was determined to be 37.0 kJ mol−1, which was competitive when compared to similar catalysts for this reaction. A study of the reusability of this catalyst suggests that the catalyst can be used multiple times consecutively with no loss in hydrogen generated. This material presents an opportunity for a sustainable catalyst to optimize the amount of hydrogen generated via the hydrolysis of NaBH4. [ABSTRACT FROM AUTHOR]

Density functional theory (DFT) was used to investigate the three-component coupling reactions of aldehydes, alkynes, and amines (A3 coupling) using N-heterocyclic carbene silver as the catalyst. This study reveals that the addition reaction between the catalyst N-heterocyclic carbene silver and phenylacetylene (PAE) forms Ag_PAE. Subsequently, one hydrogen atom of the Ag_PAE migrates to the nitrogen atom of the Amine. Thereafter, the amine aldehyde condensation reaction generates a molecule of water and an imine ion with (Path one) or without (Path two) another amine catalyst. Path one has a lower reaction barrier than Path two. Subsequently, the imine ion reacts with silver phenylacetylide to generate the A3 coupling reaction product propargylamine (PPA). Furthermore, the triple bond and −N3 group in PPA undergo a cycloaddition reaction and generate the final product (PR). The entire reaction is strongly exothermic, and, therefore, the reaction is easy to conduct. Moreover, conceptual density functional theory calculations confirm the reaction mechanism. Investigating the mechanism of these reactions will be helpful for understanding and developing new synthesis strategies for similar functional compounds. [ABSTRACT FROM AUTHOR]

CO2 electrochemical reduction (CO2 ER) from (bi)carbonate feed presents an opportunity to efficiently couple this process to alkaline-based carbon capture systems. Likewise, while this method of reducing CO2 currently lags behind CO2 gas-fed electrolysers in certain performance metrics, it offers a significant improvement in CO2 utilization which makes the method worth exploring. This paper presents two simple modifications to a bicarbonate-fed CO2 ER system that enhance the selectivity towards CO. Specifically, a modified hydrophilic cathode with Ag catalyst loaded through electrodeposition and the addition of dodecyltrimethylammonium bromide (DTAB), a low-cost surfactant, to the catholyte enabled the system to achieve a FECO of 85% and 73% at 100 and 200 mA·cm−2, respectively. The modifications were tested in 4 h long experiments where DTAB helped maintain FECO stable even when the pH of the catholyte became more alkaline, and it improved the CO2 utilization compared to a system without DTAB. [ABSTRACT FROM AUTHOR]

Here we report the synergistic effect of OMS-2 catalysts tested in ethanol oxidation, and the effects produced by both the addition of an Fe modifier in the catalyst preparation stage, and the introduction of Ag on its surface by the impregnation method. To analyze the action of each component, the Fe-modified, Ag-containing OMS-2 catalysts with different Mn/Fe ratios were prepared. Combined XPS and XRF elemental analysis confirms the states and distribution of the Ag- and Fe-containing species between the surface and bulk of the OMS-2 catalysts, which form highly dispersed Ag species on the surface of 0.05Fe–OMS-2, and are also incorporated into the OMS-2 crystalline lattice. The cooperative action of Ag and Fe modifiers improves both reoxidation ability (TPO results) and the amount of adsorbed oxygen species on the catalyst surface. The introduction of Ag to the OMS-2 and 0.05 Fe–OMS-2 surface allows a high level of activity (T80 = 150–155 °C) and selectivity (SAc80 = 93%) towards the acetaldehyde formation. [ABSTRACT FROM AUTHOR]

It has previously been shown that an Ag/CZA catalyst can simultaneously remove NOx and soot from an oxygen-rich exhaust gas at low temperatures, by utilising the N2O generated preferentially during incomplete NOx reduction. Here, we examine the effect of reformulating the catalyst to include potassium, which is a known promoter of soot combustion. On including 2 wt% K, NOx-reduction occurs both in the absence and presence of soot, but the N2O formed does not play a part in the oxidation of soot. At higher K loadings (5, 10 and 15 wt%), NOx reduction is almost completely disabled, and only contributes to the activity of the catalyst containing 5 wt% K when tested in the presence of soot. At a loading of 20 wt% K, the potassium phase segregates, leaving NO and NH3 adsorption sites exposed. In the absence of soot, this catalyst can remove NOx by reduction on the Ag/CZA component and through nitration of the potassium phase. Although the presence of potassium lowers the onset temperature for soot oxidation to within the range of NOx reduction over Ag/CZA, the mobile K species prevents the desirable C+N2O reaction. [ABSTRACT FROM AUTHOR]

Chalcopyrite and bornite are two important copper minerals, and they often coexist. In this study, the co-bioleaching of chalcopyrite and silver-bearing bornite by mixed moderately thermophilic culture at 50 °C was investigated. The bioleaching results show that the extraction percentage of Cu for co-bioleaching of chalcopyrite (Ccp) and silver-bearing bornite (Bn) (Ccp/Bn = 3:1) was 94.6%. Compared to bioleaching of chalcopyrite or silver-bearing bornite alone, the Cu extraction percentage was greatly enhanced when they were bioleached together. The leaching residues were characterized by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Silver-bearing bornite dissolved preferentially compared to chalcopyrite, due to galvanic interactions. Simultaneously, Ag+ was released from the silver-bearing bornite into solution. Ag2S formed on the surface because Cu and Fe in the chalcopyrite were replaced by Ag+, accelerating chalcopyrite dissolution and enrichment of Ag on the surface of the chalcopyrite. [ABSTRACT FROM AUTHOR]

In this work, Ag-Fe2O3 catalysts were successfully prepared using several different methods. Our main intention was to investigate the effect of the preparation methods on the catalysts' structure and their catalytic performance for CO oxidation. The catalysts were characterized by X-ray diffraction (XRD), N2 adsorption-desorption, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), H2-temperature program reduction (H2-TPR) and inductively coupled plasma optical emission spectroscopy (ICP-OES). Ag-Fe catalysts prepared by impregnating Ag into MIL-100 (Fe) presented the best catalytic activity, over which CO could be completely oxidized at 160 °C. Based on the characterization, it was found that more metallic Ag species and porosity existed on Ag-Fe catalysts, which could efficiently absorb atmospheric oxygen and, thus, enhance the CO oxidation. [ABSTRACT FROM AUTHOR]

Ag4Bi2O5/MnO2 nano-sized material was synthesized by a co-precipitation method in concentrated KOH solution. The morphology characterization indicates that MnO2 nanoparticles with a size of 20 nm are precipitated on the surface of nano Ag4Bi2O5, forming a structure like corn on the cob. The obtained material with 60% Mn offers slightly higher initial potential (0.098 V vs. Hg/HgO) and limiting current density (-5.67 mA cm-2) at a rotating speed of 1600 rpm compared to commercial Pt/C (-0.047 V and -5.35 mA cm-2, respectively). Furthermore, the obtained material exhibits superior long-term durability and stronger methanol tolerance than commercial Pt/C. The remarkable features suggest that the Ag4Bi2O5/MnO2 nano-material is a very promising oxygen reduction reaction catalyst. [ABSTRACT FROM AUTHOR]

In this article, we developed a facile one-step hydrothermal method using dimethyl formamide (DMF) as a reducing agent for the fabrication of PdAg catalyst. The scanning electron microscope (SEM) and transmission electron microscopy (TEM) images have shown that the as-synthesized PdAg catalyst had a nanochain structure. The energy-dispersive X-ray analyzer (EDX) spectrum presented the actual molar ratio of Pd and Ag in the PdAg alloy. Traditional electrochemical measurements, such as cyclic voltammetry (CV), chronoamperometry (CA) and electrochemical impedance spectrometry (EIS), were performed using a CHI 760D electrochemical analyzer to characterize the electrochemical properties of the as-synthesized catalyst. The results have shown that the PdAg catalyst with a nanochain structure displays higher catalytic activity and stability than pure Pd and commercial Pd/C catalysts. [ABSTRACT FROM AUTHOR]

The nature and size of the real active species of nanoparticulated metal supported catalysts is still an unresolved question. The technique of choice to measure particle sizes at the nanoscale, HRTEM, has a practical limit of 1 nm. This work is aimed to identify the catalytic role of subnanometer species and methods to detect and characterize them. In this frame, we investigated the sensitivity to redox pretreatments of Ag/Fe/TiO2, Ag/Mg/TiO2 and Ag/Ce/TiO2 catalysts in CO oxidation. The joint application of HRTEM, SR-XRD, DRS, XPS, EXAFS and XANES methods indicated that most of the silver in all samples is in the form of Ag species with size <1 nm. The differences in catalytic properties and sensitivity to pretreatments, observed for the studied Ag catalysts, could not be explained taking into account only the Ag particles whose size distribution is measured by HRTEM, but may be explained by the presence of the subnanometer Ag species, undetectable by HRTEM, and their interaction with supports. This result highlights their role as active species and the need to take them into account to understand integrally the catalysis by supported nanometals. [ABSTRACT FROM AUTHOR]

In this study, the full reaction mechanism for N2O hydrogenation on silver doped Au(210) surfaces was investigated in order to clarify the experimental observations. Density functional theory (DFT) calculations were used to state the most favorable reaction paths for individual steps involved in the N2O hydrogenation. From the DFT results, the activation energy barriers, rate constants and reaction energies for the individual steps were determined, which made it possible to elucidate the most favorable reaction mechanism for the global catalytic process. It was found that the N2O dissociation occurs in surface regions where silver atoms are present, while hydrogen dissociation occurs in pure gold regions of the catalyst or in regions with a low silver content. Likewise, N2O dissociation is the rate determining step of the global process, while water formation from O adatoms double hydrogenation and N2 and H2O desorptions are reaction steps limited by low activation energy barriers, and therefore, the latter are easily carried out. Moreover, water formation occurs in the edges between the regions where hydrogen and N2O are dissociated. Interestingly, a good dispersion of the silver atoms in the surface is necessary to avoid catalyst poison by O adatoms accumulation, which are strongly adsorbed on the surface. [ABSTRACT FROM AUTHOR]

Herein, the activity of Ag and bimetallic Au-Ag catalysts, supported over Ce0.85Zr0.15O2 (CZ), was investigated in a complex stream, whose components included CO, C3H8, NO, O2, and, optionally, an injection of water vapor. In such a stream, three of the possible reactions that can occur are CO oxidation, propane combustion, and NO oxidation. The aim of these studies was to explore whether silver, due to its strong affinity to oxygen, will counteract the stabilization of oxygen by potassium. The effect of the presence of potassium ions on the activity of the monometallic silver catalysts is beneficial in the complex stream without water vapor in all three studied reactions, although it is negligible in the model CO stream. It has been shown that water vapor strongly suppresses the activity of the Ag+K/CZ catalyst, much more so than that of the Ag/CZ catalyst. The second purpose of the work was to determine whether the negative effect of potassium ions on the activity of nanogold catalyst can be countered by the addition of silver. Studies in a model stream for CO oxidation have shown that, for a catalyst preloaded with gold, the effect of potassium is nulled by silver, and the activity of AuAg + 0.15 at%K/CZ and AuAg + 0.30 at%K/CZ is the same as that of the monometallic Au catalyst. Conversely, when the reaction is carried out in a complex stream, containing CO, C3H8, NO, O2, and water vapor, the presence of water vapor leads to higher CO conversion as well as increased NO2 formation and slightly suppresses the C3H8 combustion. [ABSTRACT FROM AUTHOR]

At present, platinum-based catalysts are the best cathode catalysts, but due to their high prices, they are difficult to use widely. Under alkaline conditions, silver is a better low-cost substitute. Here, a physical preparation method—electrical discharge machining (EDM)—is used to prepare Ag0 nanoparticles. The method is simple and has a high yield. The diameter of prepared nanoparticles is about 30 nm and the nanoparticle surface is rich in defects. These defects enhance the adsorption of O2. In addition, defects can cause tensile strain on the silver catalyst, causing the d-band center of silver to move upward. The defects and the upward shift of the d-band center jointly improve the adsorption energy and catalytic performance of Ag0. This work provides a new method for the engineering construction of surface defects and the preparation of metal catalysts. [ABSTRACT FROM AUTHOR]

Initially, three samples of carbon nanotubes (SWCNTs) were synthesized from neem tree material. Afterward, these samples were coated with hexagonal boron nitride (h-BN) to form h-BN and CNT composite (h-BN-CNT). The essence of using h-BN (being a perfect insulator) with armchair SWCNT (being a conductor) is to create an interface between an insulator and conductor. The samples were treated under three different transition metal nanoparticles; silver, iron, and nickel. Thermogravimetric (TGA) analysis reveals that h-BN/CNT is thermally more stable with silver than iron and nickel nanoparticles. TGA profile showed resistance to mass loss at the beginning due to the higher thermal resistivity by the impurity compounds. The DFT calculation, generalized gradient approximation (GGA), and Perdew–Burke–Ernzerhof (PBE) analysis found engineered bandgap energy of 3.4 eV for the synthesized h-BN-CNT heterostructure. Because of its unique structural and electronic properties such as tunable bandgaps, the h-BN-CNT heterostructure may open new ways for manipulating excitons in the CNTs, and thus can be explored to develop various new electronic devices. [ABSTRACT FROM AUTHOR]

Au and Ag were deposited on TiO2 modified with Ce, La, Fe or Mg in order to obtain bimetallic catalysts to be used for liquid-phase oxidation of 1-octanol. The effects of the deposition order of gold and silver, and the nature of the support modifying additives and redox pretreatments on the catalytic properties of the bimetallic Au-Ag catalysts were studied. Catalysts were characterized by low-temperature nitrogen adsorption–desorption, energy dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy and ultraviolet-visible diffuse reflectance spectroscopy. It was found that pretreatments with hydrogen and oxygen at 300 °C significantly decreased the activity of AuAg catalysts (silver was deposited first) and had little effect on the catalytic properties of AgAu samples (gold was deposited first). The density functional theory method demonstrated that the adsorption energy of 1-octanol increased for all positively charged AuxAgyq (x + y = 10, with a charge of q = 0 or +1) clusters compared with the neutral counterparts. Lanthanum oxide was a very effective promoter for both monometallic and bimetallic gold and silver catalysts in the studied process. [ABSTRACT FROM AUTHOR]

As an important moiety in natural products, N,O-acetal has attracted wide attention in the past few years. An efficient method to construct N,O-acetal has been developed. Using silver catalyst, cyclobutenediones were smoothly converted to the corresponding γ-aminobutenolides in the presence of formamides, in which cyclobutenediones likely proceed with a key decarbonylative [3 + 2] cycloaddition process. In this way, a series of products with varied substituents were isolated in moderate yield and fully characterized. [ABSTRACT FROM AUTHOR]

Catalytic reactors performing continuously are an important step towards more efficient and controllable processes compared to the batch operation mode. For this purpose, homogenous high internal phase emulsion polymer materials with an immobilized silver catalyst were prepared and used as a continuous plug flow reactor. Porous material with epoxide groups was functionalized to bear aldehyde groups which were used to reduce silver ions using Tollens reagent. Investigation of various parameters revealed that the mass of deposited silver depends on the aldehyde concentration as well as the composition of Tollens reagent. Nanoparticles formed on the pore surface showed high crystallinity with a cuboctahedra crystal shape and highly uniform surface coverage. The example of the 4-nitrophenol catalytic reduction in a continuous process was studied and demonstrated to be dependent on the mass of deposited silver. Furthermore, productivity increased with the volumetric silver density and flow rate, and it was preserved during prolonged usage and storage. [ABSTRACT FROM AUTHOR]

The effect that UV-LED irradiation exerted on a sodium-modified silver catalyst supported on strontium carbonate (Ag-Na/SrCO3) was examined during an epoxidation of propylene to propylene oxide. Based on our previous study, we used Ag(56)-Na(1)/SrCO3 in this study. The numbers in parentheses refer to the weight percentage of silver and sodium. Although this catalyst system did not contain typical photocatalysts such as titanium oxide or tungsten oxide, UV-LED irradiation of Ag(56)-Na(1)/SrCO3 resulted in an evident improvement in the selectivity and yield of propylene oxide. Such an advantageous effect of UV-LED irradiation could not be discussed based on the bandgap used in photocatalysts and, therefore, we proposed a mechanism based on the plasmon excitation of silver, which could be accomplished using the irradiation wavelength of UV-LED to produce electrons. Since the lifespan of these electrons is expected to be short, it is difficult to place them into direct contact with the gas phase of oxygen. Once the generated electrons move to SrCO3, however, the lifespan is improved, which could allow suitable contact with oxygen in the gas phase to form active oxygen. If the oxygen is active for epoxidation as hydrogen peroxide, this could explain the improvement in activity from UV-LED irradiation. [ABSTRACT FROM AUTHOR]

This study aimed at optimizing the production of glycolic acid from glycerol catalytic oxidation over a silver catalyst supported on a mixed cerium-zirconium oxide, to progress towards the industrialization of a derived process. Optimization of the operating conditions was performed using the response surface methodology. We concluded that the production of glycolic acid depends mainly of glycerol concentration, NaOH/glycerol ratio, catalyst/glycerol ratio, and O2/glycerol ratio. The optimal conditions we found were a temperature of 60 °C, a NaOH/glycerol molar ratio of 2, an O2/glycerol molar ratio of 0.23, and a catalyst/glycerol mass ratio of 0.07. With these optimal conditions, it was possible to increase the glycerol concentration from 0.3 M to 2 M, obtaining an increase in the concentration of glycolic acid in the liquid fraction, from 0.27 mol/L of glycolic acid (with initial glycerol solution 0.3 M) to 0.88 mol/L (with initial solution 2 M), while keeping a 100% glycerol conversion. [ABSTRACT FROM AUTHOR]

Herein, it has been shown that betulin can be transformed into its biologically active oxo-derivatives (betulone, betulinic and betulonic aldehydes) by liquid-phase oxidation over supported silver catalysts under mild conditions. In order to identify the main factors determining the catalytic behavior of nanosilver catalysts in betulin oxidation, silver was deposited on various alumina supports (γ-alumina and boehmite) using deposition–precipitation with NaOH and incipient wetness impregnation methods, followed by treatment in H2 or O2. Silver catalysts and the corresponding supports were characterized by X-ray diffraction, nitrogen physisorption, inductively coupled plasma optical emission spectroscopy, photoelectron spectroscopy and transmission electron microscopy. It was found that the support nature, preparation and treatment methods predetermine not only the average Ag nanoparticles size and their distribution, but also the selectivity of betulin oxidation, and thereby, the catalytic behavior of Ag catalysts. In fact, the support nature had the most considerable effect. Betulin conversion, depending on the support, increased in the following order: Ag/boehmite < Ag/boehmite (calcined) < Ag/γ-alumina. However, in the same order, the share of side reactions catalyzed by strong Lewis acid centers of the support also increased. Poisoning of the latter by NaOH during catalysts preparation can reduce side reactions. Additionally, it was revealed that the betulin oxidation catalyzed by nanosilver catalysts is a structure-sensitive reaction. [ABSTRACT FROM AUTHOR]

Anion exchange membrane fuel cells (AEMFCs) are attractive alternatives to proton exchange membrane fuel cells due to their ability to employ nonprecious metals as catalysts, reducing the cost of AEMFC devices. This paper presents an experimental exploration of the carbon support material effects on AEMFC performance. The silver (Ag) nanoparticles supported on three types of carbon materials including acetylene carbon (AC), carbon black (CB), and multiwalled carbon nanotube (MWCNT)—Ag/AC, Ag/CB, and Ag/MWCNT, respectively—were prepared using the wet impregnation method. The silver loading in the catalysts was designed as 60 wt.% during the synthesizing process, which was examined using thermogravimetric analysis. The elemental composition of the prepared Ag/AC, Ag/CB, and Ag/MWCNT catalysts was confirmed using X-ray diffraction analysis. The nanoparticle size of Ag attached on carbon particles or carbon nanotubes, as observed by scanning electron microscopy (SEM), was around 50 nm. For the performance tests of a single AEMFC, the obtained results indicate that the maximum power density using Ag/MWCNT as the cathode catalyst (356.5 mW·cm−2) was higher than that using Ag/AC (329.3 mW·cm−2) and Ag/CB (256.6 mW·cm−2). The better cell performance obtained using a MWCNT support can be ascribed to the higher electrical conductivity and the larger electrochemical active surface area calculated from cyclic voltammetry measurements. [ABSTRACT FROM AUTHOR]

A simple and inexpensive thermal oxidation process was performed to synthesize gallium oxide (Ga2O3) nanowires using Ag thin film as a catalyst at 800 °C and 1000 °C to understand the effect of the silver catalyst on the nanowire growth. The effect of doping and orientation of the substrates on the growth of Ga2O3 nanowires on single-crystal gallium arsenide (GaAs) wafers in atmosphere were investigated. A comprehensive study of the oxide film and nanowire growth was performed using various characterization techniques including XRD, SEM, EDS, focused ion beam (FIB), XPS and STEM. Based on the characterization results, we believe that Ag thin film produces Ag nanoparticles at high temperatures and enhances the reaction between oxygen and gallium, contributing to denser and longer Ga2O3 nanowires compared to those grown without silver catalyst. This process can be optimized for large-scale production of high-quality, dense, and long nanowires. [ABSTRACT FROM AUTHOR]

Catalysts for visible-light-driven oxidative cleaning processes and antibacterial applications (also in the dark) were developed. In order to extend the photoactivity of titanium dioxide into the visible region, nitrogen-doped TiO2 catalysts with hollow and non-hollow structures were synthesized by co-precipitation (NT-A) and sol–gel (NT-U) methods, respectively. To increase their photocatalytic and antibacterial efficiencies, various amounts of silver were successfully loaded on the surfaces of these catalysts by using a facile photo-deposition technique. Their physical and chemical properties were evaluated by using scanning electron microscopy (SEM), transmission electron microscopy–energy dispersive X-ray spectroscopy (TEM–EDS), Brunauer–Emmett–Teller (BET) surface area, X-ray diffraction (XRD), and diffuse reflectance spectra (DRS). The photocatalytic performances of the synthesized catalysts were examined in coumarin and 1,4-hydroquinone solutions. The results showed that the hollow structure of NT-A played an important role in obtaining high specific surface area and appreciable photoactivity. In addition, Ag-loading on the surface of non-hollow structured NT-U could double the photocatalytic performance with an optimum Ag concentration of 10−6 mol g−1, while a slight but monotonous decrease was caused in this respect for the hollow surface of NTA upon increasing Ag concentration. Comparing the catalysts with different structures regarding the photocatalytic performance, silverized non-hollow NT-U proved competitive with the hollow NT-A catalyst without Ag-loading for efficient visible-light-driven photocatalytic oxidative degradations. The former one, due to the silver nanoparticles on the catalyst surface, displayed an appreciable antibacterial activity, which was comparable to that of a reference material practically applied for disinfection in polymer coatings. [ABSTRACT FROM AUTHOR]

Gallium oxide (Ga2O3) is a new wide bandgap semiconductor with remarkable properties that offers strong potential for applications in power electronics, optoelectronics, and devices for extreme conditions. In this work, we explore the morphology of Ga2O3 nanostructures on different substrates and temperatures. We used silver catalysts to enhance the growth of Ga2O3 nanowires on substrates such as p-Si substrate doped with boron, 250 nm SiO2 on n-Si, 250 nm Si3N4 on p-Si, quartz, and n-Si substrates by using a thermal oxidation technique at high temperatures (~1000 °C) in the presence of liquid silver paste that served as a catalyst layer. We present the results of the morphological, structural, and elemental characterization of the Ga2O3 nanostructures. This work offers in-depth explanation of the dense, thin, and long Ga2O3 nanowire growth directly on the surfaces of various types of substrates using silver catalysts. [ABSTRACT FROM AUTHOR]

This work presents, for the first time, the catalytic studies of bimetallic Ag-Ni catalysts in the oxy-steam reforming (OSR) of liquefied natural gas (LNG) to hydrogen generation. The physicochemical properties of monometallic Ni and bimetallic catalysts were investigated using various techniques, such as: BET, TPR-H2, TPD-NH3, XRD, TG and SEM-EDS. The catalytic studies showed that the promotion of 20% Ni/ZrO2 catalyst by silver (by 1 or 2 wt.%) improves the efficiency of the produced hydrogen in the oxy-steam reforming of LNG at high temperature. The promotional effect of silver on the reducibility of a Ni/ZrO2 catalyst has been proven. The interactions between Ag and Ni have been proven, and explain the catalytic activity of the catalysts in the investigated processes. TG-DTA-MS results obtained for the spent catalysts proved that the small addition of silver to monometallic nickel catalyst reduces the amount of the carbon deposit formed on the catalyst surface during the oxy-steam reforming of LNG process. Obtained results in this work confirmed that liquid natural gas processing may become an alternative to fossil fuels and confirmed the validity of the hydrogen production via oxy-steam reforming of LNG. [ABSTRACT FROM AUTHOR]

Formaldehyde is an important industrial chemical that is a strong-smelling and colorless gas. It is used in a number of processes such as making household products and building materials, glues and adhesives, resins, certain insulation materials, etc. Formaldehyde can be produced industrially using air and methanol as raw materials in the presence of metal oxide catalyst or silver-based catalyst. The operating conditions and requirements of the process depend on the type of catalyst used. Therefore, a comparative study of both processes was conducted, and the results were compared. It was observed that the silver-based catalyst process has a compact plant size since the amount of air required is halved as compared to the metal oxide process. Thus, it appears that the silver-based catalyst process is more suitable for small-scale production due to its compact size and reduced utility cost. [ABSTRACT FROM AUTHOR]

One of the challenges in the preparation of poly(methyl methacrylate) (PMMA) is to develop new catalytic systems with improved efficiency. A hybrid iron oxide silver catalyst holds promise in solving this issue. Catalysts were prepared at room temperature by a two-step technique. First, iron oxide nanoparticles were prepared by the reduction of FeCl3 using sodium borohydride (NaBH4) at room temperature. Second, magnetic nanoparticles doped with a series of Ag nanoparticles (Ag, Ag/3 –amino propyltriethoxysilane (APTES) and Ag/poly(ethyleneimine) (PEI)). The prepared catalysts were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDX), and Fourier-transform infrared spectroscopy (FTIR). The catalytic activity of Fe, Ag/Fe, PEI–Ag/Fe, and APTES–Ag/Fe in methyl methacrylate (MMA) polymerization was investigated in the presence of O2, N2, NaHSO3, and benzoyl peroxide in bulk or solution conditions. The produced polymer was characterized by gel permeation chromatography (GPC) and proton nuclear magnetic resonance spectroscopy (1HNMR). The structures of PEI–Ag/Fe and APTES–Ag/Fe are assumed. The conversion efficiency was 100%, 100%, 97.6%, and 99.1% using Fe, Ag/Fe, PEI–Ag/Fe, and APTES–Ag/Fe catalysts at the optimum conditions, respectively. Hybrid iron oxide silver nanoparticles are promising catalysts for PMMA preparation. [ABSTRACT FROM AUTHOR]

We investigated the effect of silver catalysts to enhance the growth of Ga2O3 nanowires. The growth of Ga2O3 nanowires on a P+-Si (100) substrate was demonstrated by using a thermal oxidation technique at high temperatures (~1000 °C) in the presence of a thin silver film that serves as a catalyst layer. We present the results of morphological, compositional, and electrical characterization of the Ga2O3 nanowires, including the measurements on photoconductance and transient time. Our results show that highly oriented, dense and long Ga2O3 nanowires can be grown directly on the surface of silicon. The Ga2O3 nanowires, with their inherent n-type characteristics formed a pn heterojunction when grown on silicon. The heterojunction showed rectifying characteristics and excellent UV photoresponse. [ABSTRACT FROM AUTHOR]

Gout is a form of arthritis characterized by buildup of uric acid in synovial fluid, which causes severe swelling and can harm joints, tendons, and other tissues. It affects approximately 4% of the United States population, or approximately 8.3 million people nationwide and is therefore a topic of epidemiologic consideration due to its prevalence. Gout is typically diagnosed via polarized microscopy of arthroscopically-aspirated synovial fluid, which is a costly, time-consuming, labor-intensive, and technically complex procedure, warranting a simpler and less complex method for diagnosis. Here, we propose and validate a colorimetric method which is based on the ability of uric acid to reduce silver nitrate. We also assessed how the colorimetric change can be accelerated by changing the concentration of silver nitrate or adding different silver catalysts, as well as develop a matrix bed for improved handling and ease of use. When translated to the clinic, this diagnostic method for gout will have the potential to increase diagnostic efficiency and accelerate patient care at the bedside. [ABSTRACT FROM AUTHOR]

An awareness of increasing climate and health problems has driven the development of new functional and affordable soot-oxidation catalysts for stationary sources, such as fireplaces. In this study, Al(OH)3, water glass and acidic aluminium phosphate binder materials were mixed with soot-oxidation catalysts. The effect of the binder on the performance of the Ag/La-Al2O3 catalyst was examined, while the Pt/La-Al2O3 catalyst bound with Al(OH)3 was used as a reference. Soot was oxidised above 340 °C on the Ag/La-Al2O3 catalyst, but at 310 °C with same catalyst bound with Al(OH)3. The addition of water glass decreased the catalytic performance because large silver crystals and agglomeration resulted in a blockage of the support material's pores. Pt/La-Al2O3 bound with Al(OH)3 was ineffective in a fireplace environment. We believe that AgOx is the active form of silver in the catalyst. Hence, Ag/La-Al2O3 was shown to be compatible with the Al(OH)3 binder as an effective catalyst for fireplace soot oxidation. [ABSTRACT FROM AUTHOR]

In the last few years, interest in the use of gallium oxide (Ga2O3) as a semiconductor for high power/high temperature devices and UV nano-sensors has grown. Ga2O3 has an enormous band gap of 4.8 eV, which makes it well suited for applications in harsh environments. In this work, we explored the effect of Ag thin film as a catalyst to grow gallium oxide. The growth of gallium oxide thin film and nanowires can be achieved by heating and oxidizing pure gallium at high temperatures (~1000 °C) in the presence of trace amounts of oxygen. We present the results of structural, morphological, and elemental characterization of the β-Ga2O3 thin film and nanowires. In addition, we explore and compare the sensing properties of the β-Ga2O3 thin film and nanowires for UV detection. The proposed process can be optimized to a high scale production Ga2O3 nanocrystalline thin film and nanowires. By using Ag thin film as a catalyst, we can control the growth parameters to obtain either nanocrystalline thin film or nanowires. [ABSTRACT FROM AUTHOR]

This work presents the physicochemical characterization and activity of zirconia-supported silver catalysts for the oxidation of pollutants present in diesel engine exhaust (propane, propene, naphthalene and soot). A series of silver-supported catalysts AgxZ (x = 1, 5 and 10 wt.%, Z = zirconia) were prepared, which were studied by various characterization techniques. The results show that silver is mainly found under the form of small metal nanoparticles (<10 nm) dispersed over the support. The metallic phase coexists with the AgOx oxidic phases. Silver is introduced onto the zirconia, generating Ag–ZrO2 catalysts with high activity for the oxidation of propene and naphthalene. These catalysts also show some activity for soot combustion. Silver species can contribute with zirconia in the catalytic redox cycle, through a synergistic effect, providing sites that facilitate the migration and availability of oxygen, which is favored by the presence of structural defects. This is a novel application of the AgOx–Ag/ZrO2 system in the combustion reaction of propene and naphthalene. The results are highly promising, given that the T50 values found for both model molecules are quite low. [ABSTRACT FROM AUTHOR]

Mixtures and composites of Ag/Ag2O and TiO2 (P25) with varying mass ratios of Ag/Ag2O were prepared, employing two methods. Mechanical mixtures (TM) were obtained by the sonication of a suspension containing TiO2 and Ag/Ag2O. Composites (TC) were prepared by a precipitation method employing TiO2 and AgNO3. Powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) confirmed the presence of Ag(0) and Ag2O. The activity of the materials was determined employing methylene blue (MB) as the probe compound. Bleaching of MB was observed in the presence of all materials. The bleaching rate was found to increase with increasing amounts of TiO2 under UV/vis light. In contrast, the MB bleaching rate decreased with increasing TiO2 content upon visible light illumination. XRD and XPS data indicate that Ag2O acts as an electron acceptor in the light-induced reaction of MB and is transformed by reduction of Ag+, yielding Ag(0). As a second light-induced reaction, the evolution of molecular hydrogen from aqueous methanol was investigated. Significant H2 evolution rates were only determined in the presence of materials containing more than 50 mass% of TiO2. The experimental results suggest that Ag/Ag2O is not stable under the experimental conditions. Therefore, to address Ag/Ag2O as a (photo)catalytically active material does not seem appropriate. [ABSTRACT FROM AUTHOR]