Uniform Shape Research Articles

Measuring avian bill size: comparing and evaluating 3D surface scanning with traditional size estimates in Australian birds

Unidimensional measurements for estimating bill size, like length and width, are commonly used in ecology and evolution, but can be criticised due to issues with repeatability and accuracy. Furthermore, formula‐based estimates of bill surface area tend to assume uniform bill shapes across species, which is rarely the case. 3D surface scanning can potentially help overcome some such issues by collecting detailed external morphology and direct measurements of surface area, rather than composite estimates of size. Here, we evaluate the use of 3D surface scanners on avian museum specimens to test the repeatability of 3D‐based measurements and compare these to traditional formula‐based methods of estimating bill size from unidimensional measurements. Using 28 Australian bird species, we investigate inter‐observer repeatability of surface area measurements from 3D surface scans. We then compare 3D‐based size estimates to formula‐based size estimates to infer the accuracy and precision of formula‐based measurements of bill surface area. We find that morphometric measurements from 3D surface scans are highly repeatable between observers, without the need for extensive training, demonstrating an advantage over unidimensional measuring methods, like callipers. When comparing 3D‐based measurements to formula‐based estimates of bill surface area, most formulae for estimating size consistently underestimate surface area, and with considerable variation between species. Where 3D scanning is not possible, we find that a commonly used cone formula for estimating bill size is most precise across diverse bill shapes, therefore supporting its use in interspecific contexts. However, we find that incorporating an additional unidimensional measure of bill curvature into formulae improves the accuracy of the calculated area. Our results reveal the high potential for 3D surface scanners in avian morphometric research, especially for studies necessitating large sample sizes collected by multiple observers, and gives suggestions for formula‐based approaches to estimate bill size.

Synthesis of Carbon Nanofibers using Bimetallic Nickel-Palladium Nano Catalysts and Evaluation of Charge Storage Capacity

Metal-nanoparticle (NP) catalysts play a crucial role in the chemical vapor deposition synthesis of various nanomaterials, such as nanotubes, nanofibers, and nanowires. The alloying of different metal elements offers the potential for achieving higher growth rates and improving catalyst performance and longevity. However, the precise synthesis of small and uniform metal NPs with the desired composition remains challenging due to theoretical limitations, notably the Hume-Rothery rule. In this study, nickel (Ni)-palladium (Pd) alloy NPs were successfully synthesized via the reverse micelle method, resulting in NPs characterized by consistent and uniform size and shape, with an average diameter of 2.8nm. The addition of Pd atoms to Ni to form alloy-NPs shifted the growth mode from surface diffusion to bulk diffusion, such that herringbone carbon nanofibers (CNFs) were grown with reduced diameters using CVD. These alloy catalysts maximize the physicochemical properties of herringbone CNFs for electrochemical applications. The increased number of active sites at the CNF edges considerably enhances charge storage while improving charge and discharge rates. Notably, the versatility of the alloy nanocatalysts introduced in this study extends beyond CNF synthesis, as they can also find application in the synthesis of carbon nanotubes and boron nitride nanotubes.

Optimized α/β pulse shape discrimination in Borexino

Borexino could efficiently distinguish between α and β radiation in its liquid scintillator by the characteristic time profile of its scintillation pulse. This α/β discrimination, first demonstrated on the ton scale in the counting test facility prototype, was used throughout the lifetime of the experiment between 2007 and 2021. With this method, the α events are identified and subtracted from the solar neutrino events similar to β. This is particularly important in liquid scintillators, as the α scintillation is strongly quenched. In Borexino, the prominent Po210 decay peak was a background in the energy range of electrons scattered from Be7 solar neutrinos. Optimal α/β discrimination was achieved with a , with a higher ability to leverage the timing information of the scintillation photons detected by the photomultiplier tubes. An event-by-event, high efficiency, stable, and uniform pulse shape discrimination was essential in characterizing the spatial distribution of background in the detector. This benefited most Borexino measurements, including solar neutrinos in the pp chain and the first direct observation of the CNO cycle in the Sun. This paper presents key milestones in α/β discrimination in Borexino as a term of comparison for current and future large liquid scintillator detectors. Published by the American Physical Society 2024

Chitosan-coated nanoliposome: An approach for simultaneous encapsulation of caffeine and roselle-anthocyanin in beverages

The objective of the present research was to develop chitosan-coated nanoliposomes using a modified heating method as a delivery system for simultaneous encapsulation of caffeine and roselle anthocyanin to fortify beverage. Response surface methodology was used to ascertain the optimized formulation, aiming to maximize the encapsulation efficiency, minimize the particle size, and maximize the zeta potential. The liposomes fabricated under the optimized conditions (lecithin to cholesterol ratio of 13 and wall to core ratio of 2.16) showed encapsulation efficiency values of 66.73 % for caffeine and 97.03 % for anthocyanin, with a size of 268.1 nm and a zeta potential of −39.11 mV. Fourier transform infrared spectroscopy confirmed the formation of hydrogen bonds between the polar sites of lecithin and the loaded core compounds. Thermal analysis suggested the successful encapsulation of the caffeine and anthocyanin. Transmission and scanning electron microscopy images confirmed a uniform spherical shape with a smooth surface. Fortifying the model beverage with the liposome and the chitosan-coated nanoliposome revealed higher values of encapsulation efficiency of anthocyanin (70.33 ± 3.11 %), caffeine (86.37 ± 2.17 %) and smaller size (280.5 ± 0.74 nm) of the chitosan-coated nanoliposomes at the end of 60the days. A hedonic sensory test of the fortified beverage with chitosan-coated nanoliposomes confirmed an improvement in the organoleptic properties of the beverage by masking its bitterness (receiving three more sensory scores in perceiving the bitterness intensity). Overall, our study indicates that the high potential of the chitosan-coated nanoliposomes for the simultaneous loading of the caffeine and anthocyanin, as well as their possible application in food and beverage formulations.

Anisotropic growth of gold anchors on CdSe semiconductor quantum platelets for self-assembled architectures with well-connected electronic circuits for the electrochemical detection of enrofloxacin.

Anisotropic growth of nanomaterials enables advances in building diverse and complex architectures, which exhibit unique properties and enrich the choice of nano-building modules for electrochemical sensor devices. Herein, an anisotropic growth method was proposed to anchor gold nanoparticles (AuNPs) onto both ends of quasi-two-dimensional CdSe semiconductor quantum nanoplatelets (NPLs), appearing with a monodisperse and uniform nano-dumbbell shape. Then, these AuNPs were exploited as natural anchor points and further initiated self-assembly to create complex architectures via dithiol bridges. Detailed studies illustrated that the covalent Se-Au bonds facilitate effective charge transfer in the internal metal-semiconductor (M-S) electric field. The narrowed energy gap and up-shifted highest occupied molecular orbital were favored for electron removal during the electro-oxidation process. The ultrathin CdSe NPLs supplied a large specific surface area, carrying remaining holes and abundant active sites for target electro-catalysis. As a result, using the assembled complex as the electrode matrix with well-connected electronic circuits, a reliable electrochemical sensor was achieved for enrofloxacin detection. Under the optimal conditions, the current response exhibits two linear dynamic ranges, 0.01-10.0 μM and 10.0-250 μM, and the detection limit was calculated as 0.0026 μM. This work not only opens up broad application prospects for heterogeneous M-S combinations as effective electrochemical matrixes but also develops reliable antibiotic assays for food and environmental safety.

Zein/fucoidan-coated phytol nanoliposome: preparation, characterization, physicochemical stability, in vitro release, and antioxidant activity.

To improve phytol bioavailability, a novel method of magnetic stirring and high-pressure homogenization (HPH) combination was used to prepare zein/fucoidan-coated phytol nanoliposomes (P-NL-ZF). The characterization, the simulated in vitro digestion, and the antioxidant activity of these phytol nanoliposomes from the different processes have been studied. Based on the results of dynamic light scattering (DLS) and gas chromatography-mass spectrometer (GC-MS) analysis, P-NL-ZF prepared through the combination of magnetic stirring and HPH exhibited superior encapsulation efficiency at 76.19% and demonstrated exceptional physicochemical stability under a series of conditions, including storage, pH, and ionic in comparison to single method. It was further confirmed that P-NL-ZF by magnetic stirring and HPH displayed a uniform distribution and regular shape through transmission electron microscopy (TEM). Fourier-transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC) analysis showed that electrostatic interactions and hydrogen bonding were the primary driving forces for the formation of composite nanoliposomes. Additionally, an in vitro digestion study revealed that multilayer composite nanoliposomes displayed significant and favorable slow-release properties (58.21%) under gastrointestinal conditions compared with traditional nanoliposomes (82.36%) and free phytol (89.73%). The assessments of chemical and cell-based antioxidant activities demonstrated that the coating of zein/fucoidan on phytol nanoliposomes resulted in enhanced effectiveness in scavenging activity of ABTS free radical and hydroxyl radical and mitigating oxidative damage to HepG2 cells. Based on our studies, the promising delivery carrier of zein/fucoidan-coated nanoliposomes is contributed to the encapsulation of hydrophobic natural products and enhancement of their biological activity. © 2024 Society of Chemical Industry.

Dual-Catalysts-Embedded spontaneously propelling asymmetric micromotors using triple emulsion microfluidic synthesis for highly efficient nano/microplastic removal

Plastics, which are pivotal in modern technological progress and have a broad range of applications, now pose a significant environmental and health risk globally. Despite their detrimental environmental effects, there is a lack in research on effective plastic removal and treatment strategies. Addressing this urgent issue necessitates the development of innovative and efficient materials and methods for removing plastics from contaminated environments. In this study, we utilized a microfluidic technique to create novel and eco-friendly asymmetrically structured micromotors made of glucose oxidase (GOx)/catalase (Cat) embedded in polyethylene glycol diacrylate (PEGDA). These micromotors are specifically engineered to efficiently remove substantial amounts of plastics from ecosystems. The microfluidic process enabled the production of micromotors with uniform yet asymmetric shapes through aqueous two-phase separation and UV polymerization. By incorporating functional nanomaterials, these micromotors can be customized for specific wastewater treatment needs. Our design utilizes GOx and Cat to consume glucose as fuel, generating oxygen microbubbles. These bubbles not only propel the micromotors but also capture suspended plastic nano/micro-particles, effectively removing them from aquatic environments. The high surface tension of the bubbles allows for the entrapment of plastics at their interface, facilitating their removal from the water. In addition, non-toxic nature of these GOx/Cat PEGDA micromotors makes them especially suitable for environmental remediation and biological applications, addressing the urgent need for environmentally benign solutions to plastic pollution.

Exploiting flow manipulation to engineer the electroactive phase for improved piezo response in size tunable PVDF microspheres via microfluidic technology

Polyvinylidene fluoride (PVDF), a semi-crystalline polymer with remarkable piezo-, ferro-, and pyroelectric properties in its electroactive phase (EA), holds significant potential. Microfluidic-based techniques, particularly droplet-microfluidics, have become a preferred method for producing PVDF microspheres, offering advantages like size and shape adjustability, simplicity, efficiency, and effective heat dissipation. This article focuses on employing a microfluidic flow focussing device (MFFD) with thermal initiated off-chip polymerization to process PVDF microspheres. The MFFD disperses uniform droplets into an oil bath, initiating polymerization and yielding microspheres ranging from 126 to 754 µm. Fine-tuning flow rates achieves precise control over microparticle uniformity, monodispersity, size, and spherical shape. Optimization of reaction temperature (Toil) significantly enhances the EA phase, reaching 82.05 % at Toil = 60 °C. The resulting microspheres are comprehensively characterized for structure, morphology, composition, phase, hydrophobicity, biocompatibility, thermal, and piezoelectric properties. Additionally, machine learning analysis is employed to predict the mean diameter as well as the EA and β-phase of PVDF microspheres. A flexible piezoelectric device made from PVDF microspheres, demonstrating an open circuit voltage of ∼23.5 V in response to finger and foot tapping movements, showcases potential for self-powered wearable sensors and devices. This study underscores the synergy of microfluidics, polymer science, and artificial intelligence in advancing smart materials.

Multivariate Bayesian Optimization of CoO Nanoparticles for CO2 Hydrogenation Catalysis.

The hydrogenation of CO2 holds promise for transforming the production of renewable fuels and chemicals. However, the challenge lies in developing robust and selective catalysts for this process. Transition metal oxide catalysts, particularly cobalt oxide, have shown potential for CO2 hydrogenation, with performance heavily reliant on crystal phase and morphology. Achieving precise control over these catalyst attributes through colloidal nanoparticle synthesis could pave the way for catalyst and process advancement. Yet, navigating the complexities of colloidal nanoparticle syntheses, governed by numerous input variables, poses a significant challenge in systematically controlling resultant catalyst features. We present a multivariate Bayesian optimization, coupled with a data-driven classifier, to map the synthetic design space for colloidal CoO nanoparticles and simultaneously optimize them for multiple catalytically relevant features within a target crystalline phase. The optimized experimental conditions yielded small, phase-pure rock salt CoO nanoparticles of uniform size and shape. These optimized nanoparticles were then supported on SiO2 and assessed for thermocatalytic CO2 hydrogenation against larger, polydisperse CoO nanoparticles on SiO2 and a conventionally prepared catalyst. The optimized CoO/SiO2 catalyst consistently exhibited higher activity and CH4 selectivity (ca. 98%) across various pretreatment reduction temperatures as compared to the other catalysts. This remarkable performance was attributed to particle stability and consistent H* surface coverage, even after undergoing the highest temperature reduction, achieving a more stable catalytic species that resists sintering and carbon occlusion.

Enhancing luminescence of AF2: Ln3+ (A = Ca, Sr; Ln = Eu, Tb) by the use of carbon dots

Lanthanide ions-doped fluoride nanocrystals have excellent application prospect. However, low photoluminescence quantum yield (PLQY) is usually along with lanthanide ions-doped fluoride nanocrystals owing to their low molar absorptivity and narrow absorption band. In order to increase the absorption cross section of Ln3+ in fluoride nanocrystals, a facile synthesis strategy to enhance luminescence of AF2: Ln3+ (A = Ca, Sr; Ln = Eu, Tb) by the use of carbon dots (CDs) has been developed in this work. A series of characterizations including TEM, XRD, FTIR and XPS demonstrated that the CDs have been successfully combined with the surface of AF2: Ln3+ nanocrystals. The combination of CDs has little influence on the microstructure and phase structure of AF2: Ln3+, and CDs@AF2: Ln3+ nanocrystals have uniform and regular shape with cubic phase. CDs are used as a broadband sensitizer and lead to the broadband excitation of Ln3+, resulting in the enhancement around 10-fold of Ln3+ luminescence emission in AF2: Ln3+ nanocrystals after CDs combination. The corresponding PLQY increases almost three times, and the luminescence enhancement mechanism by combining CDs is proposed. In addition, the CDs@AF2: Ln3+ nanocrystals are used to prepare CDs@AF2: Ln3+/PVA films, which exhibits excellent luminescence properties under the excitation of UV light. This work provides a superior method for enhancing the luminescence properties of lanthanide ions-doped nanocomposites and demonstrates practical potential as promising candidates for light-converting thin films.

Zn complexed on hybrid manganese doped cobalt ferrite nanoparticles covered by silica as a catalyst in the synthesis of 2-amino-4H-pyran and N- arylquinoline derivatives

In the present work, Zn complexed on hybrid manganese doped cobalt ferrite nanoparticles covered by silica were synthesized. These MNPs were characterized using different techniques including Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction analysis (XRD), Field emission‐scanning electron micro-scope (FE-SEM), Energy‐dispersive X‐ray spectroscopy (EDS), Vibration sample magnetometer (VSM), Inductively coupled plasma atomic emission spectroscopy (ICP), Zeta potential and Thermogravimetric analysis (TGA). FE-SEM Images showed uniform spherical shape with rough surfaces and an aggregation in structure of MNPs. A decrease in Ms is visible in VSM analysis due to the increase in particle diameter as a result of loading the organic coating on the surface of the magnetic nanoparticles. According to TGA analysis, the synthesized MNPs have good stability up to 125 °C. The ICP analysis indicates the presence of 0.13 mmol/g zinc on the surface of loaded MNPs. The effect of these prepared MNPs as a catalyst was studied in the synthesis of 2-amino-4H-pyran and N- arylquinoline derivatives. This method provides excellent yield of products with short reaction time, simple purification and easy separation of the catalyst. Furthermore, the reusability of the catalyst during five periods was not associated with a significant decrease in its activity.

Fast fabrication of High-Yield WS2 nanoscrolls via ultrasound sonication

Transforming the bulk of tungsten disulfide (WS2) into one-dimensional (1D) nanoscrolls has potential applications in a variety of fields. The current methods for fabricating (1D) WS2nanoscrolls suffer from low yields, high temperatures, a complicated fabrication process, and the use of surfactants. We have reported a facile and cost-effective approach for fabricating WS2 nanoscrolls in high yield using ultrasound probe sonication (20 KHz) from bulk WS2 in dimethylformamide (DMF) in two hours. Importantly, this simple method achieves a 90 % WS2 nanoscroll yield.This depends on critical experimental parameters such as the choice of solvent, the initial concentration of WS2, and the sonication time. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) measurements confirm that the nanoscrolls have a closely uniform shape, with an interlayer spacing of ∼ 0.62 nm between adjacent layers of WS2 nanoscrolls. Atomic force microscopy (AFM) reveals that the nanoscrolls have a length of approximately 650 nm and a height profile of 5–10 nm, indicating their formation from multiple layers of WS2. We further investigate the fabricated nanoscrolls using other techniques such as X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Raman spectroscopy.

The Quality Analysis of Of Rolled Pancake with Carrot Extract Substitution as Natural Food Colouring

This research aims to analyze the effect of 0%, 15%, 30% and 45% substitution of carrot extract to the quality of rolled pancakes in terms of shape, color, aroma, texture and taste. This research was conducted in August 2023 at the Culinary Workshop, Department of Family Welfare Sciences, Faculty of Tourism and Hospitality, Padang State University. This type of research is a pure experiment using a completely randomized design method consisting of 4 treatments and 3 repetitions. The data used is primary data obtained from 3 expert panelists using an organoleptic test format on the quality of rolled pancakes with the substitution of carrot extract. The data obtained was then tabulated in table form and analysis of variance (ANOVA) was carried out. If F count > F table then proceed with the Duncan test. The results of this research show that there is a significant effect of substitution of 0%, 15%, 30% and 45% carrot extract on the quality of color and aroma of rolled pancakes. The results of data analysis obtained the highest overall achievement scores, namely: neat shape 3.56 (45%), uniform shape 3.44 (30%), color 3.44 (45%), aroma 3.67 (45%), texture 3.67 (45%) and taste 4.00 (45%). The results of the quality test for rolled pancakes with the best carrot extract substitution were 45% (X3).

The Effect Of Addition Skipjack Tuna On The Quality Of Wet Corn Noodles

Wet corn noodles are a food product made from wheat flour with the addition of corn flour. This research aims to analyze the effect of adding 10% skipjack tuna on the quality of shape, color, texture, aroma and taste of wet corn noodles. This type of research is experimental using the Independent Sample T-test method. The data used is primary data obtained directly from three expert panelists by filling in the organoleptic test format for the quality of wet corn noodles with the addition of skipjack tuna and secondary data from journals. The data obtained was then tabulated in table form and a level test was carried out on each variable X1 and X2 to find out whether there was a mean comparison for these variables using the Independent Sample T-test. The results of this research show that there is an effect of adding 10% of skipjack tuna on the quality of shape, color, texture, aroma and taste. The results of data analysis obtained the highest overall achievement scores, namely neat shape quality 3.78 (quite neat), uniform shape quality 3.89 (quite uniform), color quality 2.78 (less yellow), springy texture quality 3.67 (fair chewy), easy to break texture quality 2.22 (less easy to break), aroma quality 3.78 (quite a typical wet noodle aroma), taste quality 3.78 (quite tasty). Test results for the best quality of wet corn noodles with the addition of skipjack tuna in treatment X2 with the addition of 10% skipjack tuna.

The Effect Of Substituting Butterfly Pea Extract As A Natural Dye In Mochi Production

Mochi is a traditional Japanese food made from glutinous rice flour with a sweet taste and a distinctive soft texture that turns chewy when eaten. Mochi is typically round in shape, filled with peanut paste, and coated with roasted cornstarch. In Indonesia, mochi has various variations, one of which involves modifying the mochi's outer layer by adding food coloring to the dough. As time progresses, people have become more aware of the negative effects of synthetic ingredients, leading consumers to shift towards using natural food colorings. Butterfly pea flowers are one alternative source of natural food coloring. These flowers contain anthocyanin compounds that can produce a blue color. The use of butterfly pea flowers does not affect the taste of food products since it only contains anthocyanins. The purpose of this study is to analyze the quality of mochi with the addition of butterfly pea flower extract. The research method employed is a pure experiment, using a Completely Randomized Design (CRD) with three repetitions. Data was collected by surveying a limited group of panelists, who are Family Welfare Science lecturers with a concentration in Culinary Arts at the Faculty of Tourism and Hospitality, Universitas Negeri Padang. Data was analyzed using Analysis of Variance (ANOVA), and if F-value > F-table, then the Duncan test was conducted. The research results indicate a significant effect on color quality. However, the shape (neat and uniform), aroma, texture, and taste did not show a significant effect. The highest overall scores were as follows: neat shape 3.11 (X1), uniform shape 3.11 (X1), blue color 3.44 (X1), pleasant aroma 3.33 (X0), chewy texture 3.67 (X1), and sweet taste 3.33 (X1). The best result in this study was treatment (X1) with a 50% substitution of butterfly pea flower extract.

The Influence of Tacrolimus on Cellular Morphology, Cellular Viability, Osteogenic Differentiation, and mRNA Expression within Stem Cell Spheroids.

Background and Objectives: Tacrolimus is a macrolide lactone compound derived from the bacterium Streptomyces tsukubensis, widely known as an immunosuppressant. In basic research, the effects of tacrolimus on osteogenic differentiation have been tested using mesenchymal stem cells. In this study, tacrolimus's effects on the cellular survival and osteogenic differentiation of stem cell spheroids were investigated. Materials and Methods: Concave microwells were used to form stem cell spheroids in the presence of tacrolimus at final concentrations of 0 μg/mL, 0.1 μg/mL, 1 μg/mL, 10 μg/mL, and 100 μg/mL. A microscope was used to test cellular vitality qualitatively, and an assay kit based on water-soluble tetrazolium salt was used to measure cellular viability quantitatively. Alkaline phosphatase activity and an anthraquinone dye test for measuring calcium deposits were used to assess osteogenic differentiation. To assess the expression of osteogenic differentiation, a quantitative polymerase chain reaction, Western blot, and RNA sequencing were performed. Results: Spheroids across all concentrations maintained a relatively uniform and spherical shape. Cell viability assay indicated that tacrolimus, up to a concentration of 100 μg/mL, did not significantly impair cell viability within spheroids cultured in osteogenic media. The increase in calcium deposition, particularly at lower concentrations of tacrolimus, points toward an enhancement in osteogenic differentiation. There was an increase in COL1A1 expression across all tacrolimus concentrations, as evidenced by the elevated mean and median values, which may indicate enhanced osteogenic activity. Conclusions: This study showed that tacrolimus does not significantly impact the viability of stem cell spheroids in osteogenic media, even at high concentrations. It also suggests that tacrolimus may enhance osteogenic differentiation, as indicated by increased calcium deposition and COL1A1 expression. These findings advance our understanding of tacrolimus's potential roles in tissue repair, regeneration, and stem cell-based therapeutic applications.

Wireless Gas Sensor Based on the Mesoporous ZnO-SnO2 Heterostructure Enables Ultrasensitive and Rapid Detection of 3-Methylbutyraldehyde.

Achieving ultrasensitive and rapid detection of 3-methylbutyraldehyde is crucial for monitoring chemical intermediate leakage in pharmaceutical and chemical industries as well as diagnosing ventilator-associated pneumonia by monitoring exhaled gas. However, developing a sensitive and rapid method for detecting 3-methylbutyraldehyde poses challenges. Herein, a wireless chemiresistive gas sensor based on a mesoporous ZnO-SnO2 heterostructure is fabricated to enable the ultrasensitive and rapid detection of 3-methylbutyraldehyde for the first time. The mesoporous ZnO-SnO2 heterostructure exhibits a uniform spherical shape (∼79 nm in diameter), a high specific surface area (54.8 m2 g-1), a small crystal size (∼4 nm), and a large pore size (6.7 nm). The gas sensor demonstrates high response (18.98@20 ppm), short response/recovery times (13/13 s), and a low detection limit (0.48 ppm) toward 3-methylbutyraldehyde. Furthermore, a real-time monitoring system is developed utilizing microelectromechanical systems gas sensors. The modification of amorphous ZnO on the mesoporous SnO2 pore wall can effectively increase the chemisorbed oxygen content and the thickness of the electron depletion layer at the gas-solid interface, which facilitates the interface redox reaction and enhances the sensing performance. This work presents an initial example of semiconductor metal oxide gas sensors for efficient detection of 3-methylbutyraldehyde that holds great potential for ensuring safety during chemical production and disease diagnosis.

Droplet Formation and Energy Input during Induction Wire Melting with Pulsed and Constant Generator Power

Induction heating is a fast, reproducible, and efficient heating method used in various manufacturing processes. However, there is no established additive manufacturing (AM) process based on induction heating using wire as feedstock. This study investigates a novel approach to AM based on inductive heating, where a steel wire is melted and droplets are detached periodically using a two-winding induction coil. The process parameters and energy input into the droplets are characterized. The induction generator exhibits a sluggish response to the excitation voltage, resulting in a lag in the coil current. The process is captured using a high-speed camera, revealing a regular droplet formation of 14 Hz and uniform shapes and sizes between 2.11 and 2.65 mm in diameter when operated within an appropriate process window. Larger drops and increased spatter formation occur outside this window. The proposed method allows for the production of droplets with almost spherical shapes. Further analysis and characterization of droplet formation and energy input provide insights into process optimization and indicate an overall efficiency of approximately 10%.

Particle size dependence of nanoclustered ceria abrasives on surface activity and chemical mechanical planarization performance

The particle size of cerium oxide (ceria) abrasives plays a crucial role in the design and development of advanced self-stopping slurries for the chemical mechanical planarization (CMP) process in semiconductor device manufacturing. However, a lack of ceria nanoparticles (NPs) with a narrow size distribution and uniform shape poses challenges in investigating the fundamental principles of the relationship between abrasive size and CMP performance. In this study, we thoroughly investigated the effect of ceria NP size on the removal rate (RR) of silicon oxide using uniform-sized nanoclustered (NC) ceria NPs with three diameters: 51.4 nm (NC51), 68.6 nm (NC69), and 108.0 nm (NC108). While all three types of ceria NPs shared a crystallinity of ∼ 70.6 %, they exhibited distinct physicochemical characteristics. As the particle size decreased, the specific surface area and chemical activity (i.e., Ce3+/Ce4+) increased by 155 % and 69 %, respectively. In the CMP process, where direct contact between the abrasives and wafer occurs, the abrasive size influences CMP performance. Experimentally, NC51 achieved the highest RR among the three slurries, along with complex size-dependent contact properties and chemical activities. These experimental results offer significant insights into precise semiconductor manufacturing in a practical manner.

In-situ generation of enhanced Pd-Co nanoparticles using various stabilizing agents decorated on reduced graphene oxide as electrocatalyst for oxygen reduction reaction

The synthesis and characterization of PdCo nanoparticles deposited on reduced graphene oxide as an electrocatalyst for the oxygen reduction reaction have been successfully carried out. This research aims to investigate the influence of various stabilizing agents on the character of the metal nanoparticles towards the activity of the oxygen reduction reaction (ORR). Reduced graphene oxide (RGO) acts as a supporting material for the PdCo nanoparticles. This material was produced from graphite as a raw material that was oxidized using the Tour method. The PdCo/RGO material was synthesized by in-situ generation with the various stabilizing agent types of cetyltrimethylammonium bromide (CTAB), hexamethylenetetramine (HMTA) and a combination of CTAB-HMTA. The results showed that the optimal stabilizing agent type for PdCo/RGO is HMTA (PdCo-H/RGO), giving PdCo nanoparticles with the smallest size, the most uniform shape and the most dispersion on the RGO surface. The ORR catalytic test showed that PdCo-H/RGO displayed activity, with the number of electron transfers being 3.64, which follows the direct 4-electron reduction pathway of the ORR. The catalyst stability test showed that PdCo-H/RGO had relatively high durability with an E1/2 negative shift of 57.6 mV.