Silica nanosheets (SiO₂-NS) have drawn extensive interest in recent years due to their unique characteristics, including high specific surface area, narrow pore size distribution, high mechanical strength, controllable surface chemistry, and biocompatibility. Such characteristics make them excellent candidates for various applications, particularly in adsorption and sensing. However, the wet chemical synthesis of free-standing silica nanosheets with controllable thickness and textural properties remains a significant challenge. Here, we report synthetic method to synthesize flat, layered mesoporous silica nanosheets (SiO₂-NS) by chemical reduction of silicon tetrabromide (SiBr₄) using cetyltrimethylammonium bromide (CTAB) as a soft lamellar micelle template in a water–ethanol mixed solvent system. The resulting silica nanosheets exhibit lateral dimensions of 100–200 nm and ultrathin thicknesses of approximately 1 nm. The synthesized SiO₂-NS possesses outstanding textural properties, including a BET surface area of 971 m 2 g −1 , a mean BJH pore diameter of 2.56 nm, and a total pore volume of 0.73 cm 3 g −1 . These structural properties enable the nanosheets to function as high-performance amine sorbents and, most significantly, highly sensitive room-temperature trimethylamine (TMA) sensors. The sensors exhibit a brief recovery time and rapid response, which demonstrates the material’s promise in medical diagnostics, environmental monitoring, and food quality applications. Graphical abstract Inorganic synthesis of silica with different morphologies as a function of CTAB concentration, and the evolution of silica nanosheets

Craniofacial bone regeneration represents a dynamic area within tissue engineering and regenerative medicine. Central to this field, is the continual exploration of new methodologies for template fabrication, leveraging established bio ceramic materials, with the objective of restoring bone integrity and facilitating successful implant placements. Photopolymerized templates were prepared using three distinct bio ceramic materials, specifically a wet chemically synthesized bioactive glass and two commercially sourced hydroxyapatite variants. These templates underwent comprehensive characterization to assess their physicochemical and mechanical attributes, employing techniques including Fourier transform infrared spectroscopy, scanning electron microscopy, and nano-computed tomography. Evaluation of their biocompatibility was conducted through interaction with primary human osteoblasts (hOB) and subsequent examination using scanning electron microscopy. The results demonstrated that composite showed intramolecular hydrogen bonding interactions with the photopolymer, while computerized tomography unveiled the porous morphology and distribution within the templates. A relatively higher porosity percentage (31.55 ± 8.70

Recent investigations reveal an increasing interest in detecting toxic substances that, if present in the environment at low concentrations, can cause serious health conditions. Moreover, some of these toxic substances can be found as gases in human breath due to disease. Nanomaterial-based sensors have emerged as a crucial area of research for this purpose. This study focuses on silver-doped tungsten oxide nanoparticles (Ag/WO3) as nanosensors capable of detecting trace amounts of toxic gases at room temperature. These gases include Hydrogen sulfide (H2S), as well as other toxic gases like acetone, Ammonia (NH3), Ethanol (C2H5OH), and Acetone ((CH3)2CO). The gas-sensing behavior of Ag/WO3 nanosensors was investigated at extremely low concentrations of these gases. X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) surface, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM) were employed to analyze the material's structure and chemical state. The sensor exhibited sensitivity to gas concentrations as low as 0.25 ppm, with a robust response of up to 80

Ternary NiO/Ag/TiO2 heterojunction photocatalyst was prepared by deposition coprecipitation for visible light photocatalytic applications. Physicochemical properties of the synthesized NiO/Ag/TiO2 composite were characterized by X-ray diffraction, Brunauer-Emmett-Teller surface area measurement method, transmission electron microscopy, energy-dispersive X-ray spectroscopy techniques, X-ray photoelectron spectroscopy technique, and ultraviolet-visible absorption spectroscopy. The results suggest that the well-dispersed small metallic silver nanoparticles (<3 nm) facilitate electron transfer and bridge nickel oxide and titanium oxide. The photocatalytic degradation and the methylene blue (MB) dye kinetics were carried out on a ternary NiO/Ag/TiO2 composite and compared to bare TiO2 under visible light irradiation. The results indicate that NiO/Ag/TiO2 has superior MB photodegradation efficiency with a high reaction rate constant and low degradation time (93.15% within 60 min) compared to Ag/TiO2, NiO/TiO2, and bare TiO2. NiO/Ag/TiO2 nanocomposite was also investigated for the most common pharmaceutical waste degradation and exhibited excellent degradation efficiency. The enhancement of the composite's performance could be attributed to the surface plasmonic resonance of the Ag nanoparticles, the formation of Schottky junctions at the Ag-TiO2 and Ag-NiO interface, and the p-n heterojunction between NiO and TiO2. Ag NPs act as a photosynthesizer and a photocatalyst, facilitate electron transfer, shift the absorption to the visible light region, reduce the band gap of TiO2, suppress the electron-hole recombination, and enhance the photocatalytic activity and stability as a result.

The oxidation of Carbon monoxide (CO) to Carbon dioxide (CO2) is one of the most extensively investigated reactions in the field of heterogeneous catalysis, and it occurs via molecular rearrangements induced by catalytic metal atoms with oxygen intermediates. CO oxidation and CO2 capture are instrumental processes in the reduction of green-house gas emissions, both of which are used in low-temperature CO oxidation in the catalytic converters of vehicles. CO oxidation and CO2 adsorption at different temperatures are evaluated for palladium-supported silica aerogel (Pd/SiO2). The synthesized catalyst was active and stable for low-temperature CO oxidation. The catalytic activity was enhanced after the first cycle due to the reconditioning of the catalyst’s pores. It was found that the presence of oxide forms of palladium in the SiO2 microstructure, influences the performance of the catalysts due to oxygen vacancies that increases the frequency of active sites. CO2 gas adsorption onto Pd/SiO2 was investigated at a wide-ranging temperature from 16 to 120 °C and pressures ∼1 MPa as determined from the isotherms that were evaluated, where CO2 showed the highest equilibrium adsorption capacity at 16 °C. The Langmuir model was employed to study the equilibrium adsorption behavior. Finally, the effect of moisture on CO oxidation and CO2 adsorption was considered to account for usage in real-world applications. Overall, mesoporous Pd/SiO2 aerogel shows potential as a material capable of removing CO from the environment and capturing CO2 at low temperatures.

Low-temperature carbon monoxide (CO) oxidation on silver/silica aerogel (Ag/SiO2 AG) catalyst prepared by one-pot sol-gel synthesis followed by supercritical ethanol drying method is reported. Highly stable and sinterproof catalyst led to easy reactant diffusion to the active sites. The Ag/SiO2 AG catalyst showed enhanced catalytic activity toward low-temperature CO oxidation by preventing agglomeration of silver nanoparticles inside pores and facilitating well-dispersed active sites to enhance the mass heat transfer in the mesopores. Catalyst pretreatment conditions were found to play a crucial role in achieving high CO conversion efficiency at low light-off temperatures. Inverse counter-clockwise CO oxidation hysteresis was found to occur after the first run. The active sites contributing to this enhanced catalytic behavior were confirmed to be Ag0 from XPS, XRD, and TEM analysis. The catalyst exhibited good thermal stability up to 450 degrees C over repeated number of cycles.

Several metal oxides, such as tungsten oxide (WO3), are considered superior sensing materials for hydrogen sulfide (H2S) detection in the ambient environment. In this study, silver loaded tungsten oxide nanoparticles were prepared by microwave-assisted chemical route. Nanoparticle thin films were deposited on substrates with electrical electrodes to explore their gas sensing and electrical properties. The morphology, crystal structure, and chemical state were examined using x-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and x-ray photoelectron spectroscopy (XPS). The sensing properties of the sample were tested at different temperatures varying from room temperature to 200 degrees C. The Ag2O/WO3 nanoparticles showed enhanced H2S sensing abilities at very low temperatures (close to room temperature) and concentrations as low as 10 ppm compared to bare WO3. Moreover, the effect of annealing and comparison with physical mixing was studied and showed that non-annealed Ag-loaded WO3 produced the best response. The results can be attributed to the decrease in the energy bandgap due to increasing the Ag content and the strong interaction between the Ag and WO3 and silver to silver oxide transformation at low annealing temperatures. This study demonstrates that Ag2O/WO3 sensors offer enhanced low-temperature sensing with reasonable response time, low operating power, and simple fabrication that can be promising sensors for H2S, which may be utilized as wearable devices and in the industrial setting. (C) 2021 The Authors. Published by Elsevier B.V.

Nanomaterial such as metals and metal oxide photocatalysts have emerged as important tools for removing contaminants from wastewater and as antibacterial agents to prevent infections; this is mainly due to their stability under different irradiation conditions. Herein, the catalytic and antimicrobial activities of nanocrystalline silver (Ag), supported on tungsten oxide (WO3) nanoparticles prepared using the deposition-precipitation synthesis technique, are studied. The synthesized material was characterized as XRD, XPS, TEM, and TEM-EDS to investigate their physio-chemical properties. HRTEM, XPS analysis shows that the photocatalyst has a large sheet-like morphology with well-dispersed small metallic Ag particles (<3 nm) on the WO3 nanoparticle's surface, with most particles near the edges. Ultraviolet–visible spectra analysis observed a large redshift in the absorbing band edge and decreased bandgap energy from 2.6 to 2.1 eV. Photocatalytic analysis at different concentrations of 1% Ag/WO3 under visible light indicated a high degradation efficiency. The largest degradation efficiency of Methylene Blue (MB) under visible light irradiation was (∼80%) in 120 min at 1 g/L catalyst dosage. The photodegradation of MB under visible light as a function of catalyst dose followed the pseudo-first-order kinetics. In addition, the catalyst shows high degradation efficiency and significant dose-dependent inhibition of Gram-negative E. Coli and the Gram-positive S. aureus. Furthermore, the catalyst showed excellent stability and recyclability.

Tumor-derived exosomes may provide biomarkers for cancer treatment. Using sputtering technology, an affinity-based device to capture exosomes was developed using nanoporous substrate (NPG)-coated silicon microscopy. Immunology-based techniques detect and purify exosomes using gold coating with a specific antigen. Inverted fluorescent microscopy was used to detect target exosomes quantitatively utilizing fluorescent nanospheres as the label. We quantified the expression of CD63 surface protein markers on exosomes from conditioned culture media of breast cancer cells. The exosomes that targeted specific proteins with controls were statistically analyzed and compared to those that targeted non-specific proteins. Results from SEM showed that the exosomes were circular, between 30 and 150 nanometers in size. The porous gold substrates captured more exosomes than the nonporous substrates. Nitric acid treatments at different times resulted in a variety of pore sizes. Despite the increase in the size of the pores, the number of exosomes found in the porous gold substrate treated for 10 min nearly doubled compared to the one treated for 5 min. In this work, a fluorescence biosensor was developed to detect breast cancer exosomes using nanoporous gold substrates (NPG). Assay and model exosomes of specific breast cancer cells showed that exosomes exhibit diagnostic surface protein markers, reflecting the protein profile of their parent cells. Furthermore, the specific binding between the exosome surface antibodies and the targets identified the CD63 biomarkers on the exosome, suggesting these markers' diagnostic potential. This study can accelerate exosome research in determining tumor-related exosomes and develop novel cancer diagnostic methods.

The catalyst morphology, metal-support interaction, and reaction conditions greatly influence the catalytic performance and reaction dynamics. Similarly, the dispersion of the metal within the support plays a crucial role in the thermal stability and sintering of the catalyst. Furthermore, temperature-dependent conversion hysteresis is well-known to occur during ignition and extinction of exothermic CO oxidation over supported Pd catalysts due to the variation of CO adsorption on the surface or bulk oxidation of Pd and the ability of the catalyst to regenerate the active sites. Herein, the catalytic performance and the hysteresis behavior of mesoporous silica aerogel supported Pd (Pd/a-SiO2), and commercial fumed silica-supported Pd (Pd/f-SiO2) were investigated and compared using CO oxidation as a probe reaction under different reaction conditions and operating parameters (i.e., catalyst weight, ramp rate, and flow rate). Surface and morphologic examination using XPS, FTIR, and TEM of Pd/a-SiO2 and Pd/f-SiO2 reveal a strong correlation between the catalyst surface and structure and its catalytic performance and stability under different reaction parameters. Moreover, this study presents the effect of surface area, particle size, and size distribution on diffusion and mass transport of reactants (CO, O2) and products (CO2) and active sites accessibility. This study showed that Pd/f-SiO2 had better efficiency under high (turbulence) flow. Moreover, intrinsic apparent activation energy (Ea) and the number of active sites were calculated from the Kinetics of CO oxidation fitted using Arrhenius plots indicate that the ramp rate has less effect on Pd/f-SiO2 catalytic behavior. Even though, Pd/f-SiO2 had higher relative active sites than Pd/a-SiO2, (Ea) was lower. Cyclic stability and long-term stabilities showed that both catalysts are stable and can regenerate the active sites. The current study contributes to understanding the catalysts' surface, structural and morphological properties on the catalysts' performance toward CO oxidation and other reactions under dynamic conditions.

Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (Tig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the catalysts continue to exhibit high catalytic activity (CO conversion remains at 100%) during the extinction even at temperatures lower than Tig. The catalyst was characterized using BET, TEM, XPS, TGA-DSC, and FTIR. In this work, the influence of pretreatment conditions and stability of the active sites on the catalytic activity and hysteresis is presented. The CO oxidation on the Pd/SiO2 catalyst has been attributed to the dissociative adsorption of molecular oxygen and the activation of the C-O bond, followed by diffusion of adsorbates at Tig to form CO2. Whereas, the hysteresis has been explained by the enhanced stability of the active site caused by thermal effects, pretreatment conditions, Pd-SiO2 support interaction, and PdO formation and decomposition.

Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (Tig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the catalysts continue to exhibit high catalytic activity (CO conversion remains at 100%) during the extinction even at temperatures lower than Tig. The catalyst was characterized using BET, TEM, XPS, TGA-DSC, and FTIR. In this work, the influence of pretreatment conditions and stability of the active sites on the catalytic activity and hysteresis is presented. The CO oxidation on the Pd/SiO2 catalyst has been attributed to the dissociative adsorption of molecular oxygen and the activation of the C-O bond, followed by diffusion of adsorbates at Tig to form CO2. Whereas, the hysteresis has been explained by the enhanced stability of the active site caused by thermal effects, pretreatment conditions, Pd-SiO2 support interaction, and PdO formation and decomposition.

Hydrogen sulfide (H 2 S) presents many hazardous traits such as corrosive, explosive, toxic, and flammable. It is slightly denser than air, and a mixture of H 2 S and air can be volatile. Therefore, a reliable and robust measurement system is required to effectively detect and quantify H 2 S in many applications, such as oil and gas industries. There are several methods available in the literature to quantify H 2 S in fuel gases; however, only a few are available in case of air samples. Furthermore, array-based sensors are more reliable in the detection of volatile organic compounds (VOCs); however, sensor arrays are more expensive and challenging to produce. To overcome the limitations of producing physical sensor arrays, this article proposes a concept of virtual sensing that enables to augment a single sensing platform into a virtual array, thus, increasing the detection accuracy at no extra cost of producing a large physical sensors array. The merits of the proposed system are as follows: 1) a virtual sensing concept is combined with a physical sensing platform to enhance the proposed model’s estimation power in quantifying H 2 S in air samples; 2) a new feature extraction method based on fractional derivatives is proposed to further enhance the model’s learning capabilities; 3) an array of four gas sensors is fabricated in the in-house foundry to record and analyze the signature of H 2 S at various concentration levels; 4) a shallow neural network (NN) model is trained and tested on the recorded data, and based on the NN’s input–output relation, a mathematical model is presented for the quantification of H 2 S; and 5) the proposed model is a highly sensitive and reliable H 2 S gas sensing scheme with the ability to detect the gas instantaneously. The proposed gas quantification model has the advantages of being low cost, easy to implement, and fast operation compared with the analytical solutions. Furthermore, it is extensively tested and validated using real gas data.

In this paper we report the synthesis and characterization of tungsten oxide doped silver oxide nanostructures. The effect of silver doping on the optical and sensing properties of tungsten doped silver oxide is studied and characterized for low-temperature H 2 S gas detection. Furthermore, we investigated the sensor response, electrical characteristics, response time of tungsten oxide (WO 3 ) and tungsten oxide doped with silver oxide (Ag 2 O/ WO 3 ) at different concentrations at 25°C. The study also presents the influence of the silver oxide doping of WO3 on the H 2 S based sensors performance in terms of sensitivity and response time. The obtained results proved the possibility of synthesizing tungsten oxide-based gas sensors for future H 2 S sensor devices. UV-VIS results reveal that doping WO 3 with Ag 2 O enhanced the absorption of WO 3 in the visible region which is indicated in the red shift. Furthermore, the sensing properties of WO 3 is increased compared to bare WO 3 and Ag 2 O which shoed no response to H 2 S in this temperature range. The electrical properties of WO 3 also becomes ohmic as a result of Ag 2 O doping. The study illustrates a good way to improve the gas sensors performance through Ag 2 O doping.

In this paper, we report oxidation time effect on highly porous silver oxide nanowires thin films fabricated using ultrasonic spray pyrolysis and oxygen plasma etching method. The NW’s morphological, electrical, and optical properties were investigated under different plasma etching periods and the number of deposition cycles. The increase of plasma etching and oxidation time increases the surface roughness of the Ag NWs until it fused to form a porous thin film of silver oxide. AgNWs based thin films were characterized using X-ray diffraction, scanning electron microscope, transmission electron microscope, X-ray photoemission spectroscopy, and UV–Vis spectroscopy techniques. The obtained results indicate the formation of mixed mesoporous Ag 2 O and AgO NW thin films. The Ag 2 O phase of silver oxide appears after 300 s of oxidation under the same conditions, while the optical transparency of the thin film decreases as plasma etching time increases. The sheet resistance of the final film is influenced by the oxidation time and the plasma application periodicity. Graphic abstract

In many heterogeneous catalytic reactions, such as low-temperature CO oxidation, the preparation conditions, and the role of the CeO2 support (oxygen vacancies and redox properties) in the dispersion and the chemical state of Au, are considered critical factors for obtaining gold nanoparticle catalysts with high catalytic performance. In this work, the physical and chemical preparation methods were compared, aiming at understanding how the preparation method influences the catalytic activity. The Au/CeO2 nanoparticle catalysts with 5% Au loading were prepared via the Physical Laser Vaporization Controlled Condensation method (LVCC), and the chemical Deposition-Precipitation method (DP) was used to investigate the effect of synthesis methods on the structure and the catalytic activity toward the CO oxidation. In this manuscript, we compare the activity of nanostructured Au/CeO2 catalysts. The structure and the redox properties of the catalysts were investigated by the XRD, SEM, TEM, TPR, and XPS. The catalytic activity for low-temperature CO oxidation was studied using a custom-built quartz tube flow reactor coupled with an infrared detector system at atmospheric pressure. The study reveals that the prepared CeO2-supported Au nanoparticles’ catalytic activity was highly dependent on the preparation methods. It showed that the sample prepared by the DP method exhibits higher catalytic efficiency toward CO oxidation when compared with the sample prepared by the LVCC method. The high catalytic activity could be attributed to the small particle size and shape, slightly higher Au concentration at the surface, surface-active Au species such as Au1+, along with the large interface between Au and CeO2. This study suggests that the stability, dispersion of Au nanoparticles on CeO2, and strong interaction between Au and CeO2 lead to strong oxidation ability even below room temperature. Considering the universal character of different physical and chemical methods for Au/CeO2 preparation, this study may also provide a base for supported Au-based catalysts for many oxidation reactions in energy and environmental applications.

Synthesis of well-dispersed palladium nanoparticles within silica aerogel pores with controlled size was carried out using sol-gel synthesis under supercritical ethanol drying. The high concentration of silanol groups on silica (SiO2) surface facilitated a superior palladium (Pd) loading up to 10 wt %. The synthesized Pd/Sio(2) nanocomposite aerogels were characterized by X-ray diffraction (XRD), N2 adsorption-desorption, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and Fourier transform infrared (FTIR) spectroscopic methods. The silica aerogel supported catalysts were found to have a wide pore size distribution. TEM investigations confirmed that Pd nanocrystals were located within the SiO2 microspores and mesopores. The catalyst was evaluated for carbon monoxide (CO) oxidation reaction under ignition/extinction conditions. The synthesized catalyst demonstrated a high catalytic activity at low operating temperatures (<200 degrees C) compared to unsupported Pd nanoparticles or bare SiO2 aerogels. This enhancement in CO oxidation activity with Pd/SiO2 aerogel catalysts are attributed to the small Pd particles, Pd interaction with the surface of the underlying SiO2 and the better dispersion of Pd particles within the SiO2 pores. Porosity played a more important role during the extinction cycle as a result of the slow dissipation of the heat leading to hysteresis. We demonstrate the influence of porosity of catalyst supports on the size, dispersion, and catalytic activity of Pd nanoparticles.

The demand for renewable and alternative types of energy has taken a new dimension; the primary reason is traceable to the climate change effects that fossil-based fuels have in the earth atmosphere. Bioenergy is one of the many arrays of renewable forms of energy that have taken centre stage in replacing the conventional fossil-based energy sources. Biofuel is the liquid or gaseous fuel derived from biological processes such as agriculture (biomass) or anaerobic digestion (solid or liquid wastes) or a combination of both, rather than geological processes that are known with the traditional fossil-based counterparts. Biomass energy is readily available and environmentally friendly, because it does not lead to a net increase in carbon dioxide levels and produces low amounts of sulphur. An effective implementation of biomass in the current energy scheme would involve the development of new technologies for the large-scale production of biofuel. The two primary methods for converting biomass to biofuels are thermochemical and biochemical processes. Thermochemical conversion is a major path for producing products such as bioethanol, biodiesel, bio-oil, bio-syngas and biohydrogen. It includes fast pyrolysis, liquefaction, combustion and gasification. Liquefaction of biomass to bio-oils involves two main routes which are hydrothermal and catalytic liquefaction. Catalytic liquefaction is very similar to hydrothermal liquefaction; however, a catalyst is used to reduce the residence time, operating temperature and pressure thereby increasing the quality of liquid products. Thermochemical biofuels are getting much more attention lately as these biofuels offer several technical and strategic advantages, such as highly developed industrial infrastructure and the biofuels can be produced from virtually all sorts of available biomass in a reasonable timeframe without significant modification in the overall process. At lower reaction temperatures, thermal processing of biomass with catalytic methods offers the possibility of selectively yielding a narrow range of products and reducing the energy requirements of the transformations. In terms of catalysts used, for biodiesel production, heterogeneous catalysts in comparison to homogeneous catalysts provide more effective separation steps for products and catalysts, eliminate quenching process, and offer conditions for the continuous production process. The objective of this review is to discuss the trends, recent advances in heterogeneous catalysts and expected contribution to knowledge, specifically in nanocatalysts for biofuel production, such as metal oxide catalysts (e.g. ZnO), metal supported by metal oxide catalysts (e.g. Au-ZnO), Alloy (e.g. Cu-Co), Metal oxide supported by metal oxide (e.g. KF-CaO-Fe3O4). Our focus will be on heterogeneous catalysts.

There is a growing demand for new heterogeneous catalysts for cost-effective catalysis. Currently, the hysteresis phenomenon during low-temperature CO oxidation is an important topic in heterogeneous catalysis. Hysteresis provides important information about fluctuating reaction conditions that affect the regeneration of active sites and indicate the restoration of catalyst activity. Understanding its dynamic behavior, such as hysteresis and self-sustained kinetic oscillations, during CO oxidation, is crucial for the development of cost-effective, stable and long-lasting catalysts. Hysteresis during CO oxidation has a direct influence on many industrial processes and its understanding can be beneficial to a broad range of applications, including long-life CO2 lasers, gas masks, catalytic converters, sensors, indoor air quality, etc. This review considers the most recent reported advancements in the field of hysteresis behavior during CO oxidation which shed light on the origin of this phenomenon and the parameters that influence the type, shape, and width of the conversion of the hysteresis curves.

Cross-linked silica aerogels are promising, strong, lightweight materials for photolithographic applications. The work presented here details the preparation of ultra-lightweight aerogel materials with tailored properties through the appropriate combination of silica and methacrylate polymer using laser-induced rapid photogelation fabrication technique. For fabrication, an ethanolic solution of hexanediol diacrylate, tetraorthosilicate, Eosin Y and a tertiary amine was prepared. The amounts of reactants were varied to prepare different compositions of aerogel monoliths. The solution was irradiated with a green beam from a low power laser source. The samples, after drying in supercritical ethanol, were characterized using FTIR, BET, SEM, TGA, and a mechanical testing instrument. FTIR data suggests that neither low nor high silica content has an effect on the reactivity of acrylate functionalities during polymer formation. SEM micrographs reveal that variation in silica or polymer content does not produce any phase-separated structures. Instead, uniformly distributed nano-sized polymer–silica structures were obtained for all compositions. Our results suggest that a variety of combinations of mechanical and other properties (such as densities, surface areas, pore sizes, and pore volumes) can be produced through appropriate combination for diverse applications. All these findings provide convincing evidence that the variation of silica and/or polymer content can be used to fabricate aerogels with a variety of properties, which have the depth needed for use in laser-based 3D printing technology of simple or complex structures with nearly any dimensions.