Characteristic Peaks Research Articles

Wind farm cluster power prediction based on graph deviation attention network with learnable graph structure and dynamic error correction during load peak and valley periods

The power prediction accuracy of wind farm cluster (WFC) seriously affects its consumption and the safe and stable operation of power system. The fluctuation of power between wind farms (WFs) significantly affects the wind power ultra-short-term prediction (WPUP) accuracy of WFC. In this regard, this paper proposes a graph deviation attention network (GDAN) considering improved clustering distance and learnable graph structure (LGS) for predicting and correcting the wind power of WFC. And used a weighted distance function combining sequence convergence smoothing effect and correlation to dynamically divide the WFC, and to learn and construct the graph structure. Proposed the GDAN with LGS to mine the convergence correlation of WF sub-clusters and establish power prediction model. Considering the characteristics of load peak and valley periods (LPVP), introduced a power correction coefficient to reduce the error, and used the successive variational mode decomposition (SVMD) to extract its key components to achieve power prediction and correction. The proposed method is applied to the WFC in Western Inner Mongolia, China. Compared with the comparison model before correction, the RMSE, MAE and MAPE are reduced by 4.27 %, 3.55 % and 17.92 % respectively, and the R2 and Pr are increased by 11.87 % and 9.88 % respectively.

E-Brachy: New dosimetry package for electronic brachytherapy sources.

Large reported variability in the material composition and geometrical components of the Xoft electronic high-dose-rate brachytherapy Causes inter-source discrepancy in the source output. This variability is due to the manual manufacturing and assembly of thesources. This study aimed to develop a dosimetry software tool called E-Brachy to characterize the Xoft source and quantify the discrepancies in its photon spectrum and dosimetricproperties. E-Brachy is based on the Geant4 Monte Carlo toolkit and consists of two parts. In part one, the geometry and material composition for the source received in the computer-aided design format from the vendor were converted to the geometry description markup language format using the GUIMesh Python tool and integrated into the E-Brachy software. There was a large variation in material composition and thickness for some of the tube components. The simulation started from electrons and resulted in x-ray generations in the anode region. Multithreading, a track length estimation, and the uniform bremsstrahlung splitting variance reduction techniques were used to decrease the simulation time and increase the x-ray production. The photon energy, position, and momentum were saved into a phase space file as the photon exited the source, but before interacting with the external environment. The obtained x-ray energy spectrum was compared with measurements from the National Institute of Standards and Technology (NIST). In part two, by sampling from the generated photons, the dose rates and dosimetric parameters according to the TG-43 protocol were calculated for model S7500 and compared to the ones previously calculated for model S700 source, which were deemed identical by themanufacturer. The material composition that resulted in the most similar spectrum as the measured NIST spectrum with Pearson's correlation coefficient of 0.99 and a calculated Euclidean difference of keV was chosen for further dosimetric analysis of the model S7500 source. Characteristic peaks showed the presence of tungsten, yttrium, and silver in the source components. Differences in dose rates between the two source models surpassed 20% for polar angles , reaching a peak at cm and . The differences in the radial dose function values were within 5%. The relative difference in percentage between the anisotropy function values of the two models was closer to 0 for smaller values, but at higher polar angles, they increased to 300%. A software package called E-Brachy was successfully developed for the characterization and dosimetry of Xoft electronic brachytherapy sources. E-Brachy can be combined with spectral measurements to investigate the inter- and intra-source variability. The software package was tested by comparing the simulated spectra from the S7500 Xoft source model with NIST measurements and its TG-43 parameters with the S700 model. The TG-43 parameters between the two sources significantly exceed the recommendations ofTG-56.

Enhancing biodecolorization of Malachite Green by Flavobacterium sp. through monothetic analysis

Malachite Green (MG) is a prevalent dye in the textile industry, known for its harmful environmental impacts. Addressing the urgent need for environmentally friendly and cost-effective methods to remove MG from wastewater, this study investigated the efficacy of Flavobacterium sp., isolated from Malaysian batik wastewater, in decolorizing MG. Under shaking conditions at 160 rpm, Flavobacterium sp. exhibited a notable decolorization efficiency, with 91 % removal of MG after a 3-day incubation time, surpassing the static mode efficiency of 39 %. Further optimization using a one-factor-at-a-time (OFAT) methodology at 37 °C, pH 10, 6 % (v/v) inoculum, banana peel as the carbon source and 250 mg/L MG resulted in a remarkable enhancement, achieving 95 % decolorization within a reduced incubation time of 12 h. Moreover, repeated addition of 250 mg/L MG showed consistent and complete decolorization after 6 h by Flavobacterium sp. for four successive cycles, suggesting its economic viability for treating actual Malaysian batik wastewater. Ultraviolet–visible (UV) analysis confirmed the biodegradation of MG, evidenced by the disappearance of characteristic peaks at 618 nm and the appearance of new peaks, indicating the formation of metabolites. Flavobacterium sp. reduced pH, temperature, color, TDS, TSS, BOD and COD in batik wastewater, showing 99 % color removal efficiency. This research highlights its potential as an eco-friendly, cost-effective treatment for batik wastewater. The capacity of Flavobacterium sp. to decolorize MG in an immobilized state will be the subject of future research endeavors, aimed at elucidating the adaptability and usefulness of the biocatalyst.

An enhanced method for reconstruction of full SIF spectrum for near-ground measurements

Recently the applications of remotely sensed Solar-Induced chlorophyll Fluorescence (SIF) in the study of photosynthesis, stress conditions, and gross primary production have increased significantly. The full SIF spectrum spans over a spectral region of 650 ∼ 850 nm with two characteristic peaks around 685 nm and 740 nm. Over recent decades, many retrieval algorithms have been developed to estimate SIF at Top-Of-Canopy (TOC) using in-situ measurements of solar irradiance and canopy radiance spectra. Although the majority of retrieval methods retrieve SIF at a narrow spectral window, there exists a potential for retrieval of SIF in the full emission spectrum. Moreover, solar irradiance and canopy radiance spectra should ideally be measured at the same time but are usually measured sequentially with a certain time lag, raising potential errors in SIF retrieval. In this study, an enhanced retrieval algorithm of the full SIF spectrum at TOC is proposed. The proposed algorithm attempts to minimize the errors owing to time mismatch in measurements of solar irradiance and canopy radiance spectra. As an improvement to the previous algorithm (advanced Fluorescence Spectrum Reconstruction, aFSR), this proposed algorithm (aFSR-SVE) models the SIF-free contribution with principal components using the singular value decomposition technique. The optimal parameter settings in the forward model were determined for the experimental data collected by spectrometers used in the study. Firstly, the proposed algorithm was used to reconstruct full SIF spectrum for simulated data. The results were compared with known reference SIF values. After achieving satisfying results from simulated data, the proposed algorithm was compared with retrievals from established algorithms using experimental data. The results show improved SIF retrieval accuracy, without the need to simultaneously measure solar irradiance and canopy radiance spectra. The retrieval values comply with the results of previous algorithms in terms of spectral shape, diurnal trend, and temporal variations. The induced errors in SIF retrievals due to non-simultaneous measurements of solar irradiance and canopy radiance spectra were also investigated and the proposed algorithm was found to be less prone to such errors. Hence, the proposed algorithm is an improvement in reconstructing the full SIF spectrum with near-ground measurements. With the help of the proposed algorithm, field measurements using sequential systems and automated measurements of multiple targets can be performed effectively as it relaxes the requirement of concurrent measurement of solar irradiance and canopy radiance spectra. For future work, the applicability of this method can be investigated under more variable illumination conditions, like high cirrus clouds, passing clouds or persistent thin clouds.

Eu3+-Doped Mixed-Ligand UiO-66-Type Metal-Organic Framework for Ratiometric Fluorescence Sensing Fluoride Ions with Ultralow Detection Limit.

Metal-organic frameworks (MOFs) have emerged as a highly promising platform for various sensing applications due to their tunable structures and functionalities. In the present work, a Eu3+-doped mixed-ligand MOF, namely, the Eu3+@UiO-66-IPA, exhibited excellent luminescent properties and high fluorescence stability in aqueous media, displaying dual-emission peaks under 395 and 615 nm excitation that were readily visible to the naked eye. Importantly, the presence of fluoride ions (F-) promoted the "antenna effect" between the ligand and the Eu3+ centers, which significantly enhanced the emission intensity of the Eu3+ characteristic peak. In addition, the addition of F- also inhibited the quenching effect of high-energy O-H bonds existing in the aqueous environment. Notably, Eu3+@UiO-66-IPA demonstrated exceptional selectivity for F- over a range of competing anions, with a remarkable limit of detection as low as 0.22 μM. The developed Eu3+-doped mixed-ligand MOF system offers a highly promising strategy for the simple and accurate sensing of F- in practical applications.

Characterizing the features of the low-amplitude peaks in delta Scuti stars with TESS

Abstract The presence of low-amplitude peaks over the noise in the power spectra of δ Scuti stars is frequently disregarded. These seemingly insignificant peaks, collectively referred to as grass, might contain valuable information about the origin of these stars and the reasons behind the occurrence or absence of a plateau. It is crucial to systematically parameterize the grass phenomenon throughout a comprehensive sample that covers the entire δ Scuti star parameter range. Thus, we conduct a quantitative study of long-duration, high-duty-cycle TESS light curves, leading to improved detection methods for plateaus and a deeper understanding of their nature. This approach minimizes the impact of unresolved peaks caused by mode variations over time. Additionally, we present appropriate analysis techniques to mitigate window effects and identify and eliminate spurious peaks. We demonstrate here that the grass can be effectively parameterized based on peak density. With such parameterization two distinct regimes are found: the sparse grass regime, characterized by low peak density and the absence of a plateau in the power spectra, and the dense grass regime, characterized by high peak densities and the presence of an observable plateau. Our study is the first rigorous quantification of the emergence of such a plateau in the power spectra of δ Scuti stars. Since the grass might be related with fractality, mode variability, and stellar rotation rate, its parameterization opens a new way to analyze these stars.

Synthetic Cathinones' Comprehensive Screening and Classification by Voltammetric and Chemometric Analyses: A Powerful Method for On-Site Forensic Applications.

The use of synthetic cathinones (SCs) has increased in recent years, posing significant public health problems due to their adverse effects and potential for fatal poisonings. The structural diversity and rapid emergence of new SC analogues create challenges for law enforcement and drug screening techniques. This work presents for the first time the electrochemical detection of SCs using differential pulse voltammetry (DPV) on a boron-doped diamond electrode (BDDE). We analyzed 15 SCs, including well-known compounds such as mephedrone, methylone, and ephylone, revealing distinct electrochemical profiles with two characteristic reduction peaks (R1 and R2). The method was optimized in Britton-Robinson buffer (0.1 mol L-1, pH 8.0) and demonstrated a high selectivity and sensitivity. Multivariate statistical methods, including principal component analysis and hierarchical cluster analysis, classified SCs into six distinct groups. The DPV optimization and analytical parameter determination, including the limit of detection (LOD), were performed for the least electroactive SC, 4'-methyl-α-pyrrolidinohexanophenone, yielding an LOD of 3.8 μmol L-1, suitable for screening street samples. Interference studies with common illicit drugs and adulterants confirmed the selectivity of the DPV-BDDE method. Preliminary identification of SCs in 46 real seized samples was successfully performed using this method with results validated by liquid chromatography-mass spectrometry (LC-MS). The method also identified three SCs not included in the original set: bupropion, benzylone, and dipentylone. The DPV-BDDE method offers a rapid, robust, and portable approach for the selective screening of SCs in forensic applications, demonstrating significant advantages over traditional colorimetric tests.

The synthesis, structures and characterizations of (C5H12NO)4Cd3Cl10·2H2O and (C5H12NO)2BiCl6·H5O2 crystals

Two new organic-inorganic hybrid crystals (C5H12NO)4Cd3Cl10·2H2O and (C5H12NO)2BiCl6·H5O2 were synthesized by solution method, and their basic physical properties, including structures, thermal stability analysis, UV–Vis diffuse reflectance absorption spectra and photoluminescent characteristic were characterized. The two crystals both crystallize in same monoclinic crystal system, but different P21/c and C2/c space group for (C5H12NO)4Cd3Cl10·2H2O and (C5H12NO)2BiCl6·H5O2, respectively. Their infrared, Raman and mass spectrometry were measured, with related characteristic peaks were identified. The Raman peaks at 249 and 88 cm−1 are ascribed to Cd-Cl stretching vibration and Cl-Cd-Cl deformation vibration, respectively. The mass spectra analysis confirm the existence of C5H12NO+ cation, [CdCl]+ and Na-(C5H12NO)2BiCl6·H4O2. A phase transition peak that respectively located at 378 and 403 K for (C5H12NO)4Cd3Cl10·2H2O and (C5H12NO)2BiCl6·H5O2 was detected by the synchronous thermal analysis, which is related with the loss of crystalline water in their structures. In addition, the maximum absorption peak at 230 and 240 nm, with corresponding band gap of 3.35 and 3.15 eV were fitted for (C5H12NO)4Cd3Cl10·2H2O and (C5H12NO)2BiCl6·H5O2, respectively. Furthermore, (C5H12NO)4Cd3Cl10·2H2O features a bluish white emission with the peak centering at 496 nm when it was excited at 380 nm by a Xenon lamp. This work extends the catalog of organic-inorganic hybrid metal halides and presents the potential application of (C5H12NO)4Cd3Cl10·2H2O in optical field.

Temperature-Responsive Injectable Composite Hydrogels Based on Poly(N-Isopropylacrylamide), Chitosan, and Hemp-Derived Cellulose Nanocrystals.

Injectable and temperature-responsive Poly(N-Isopropylacrylamide) (PNIPAAm)/Chitosan composite hydrogels reinforced with cellulose nanocrystals (CNCs) were successfully fabricated via photopolymerization. 0.1-3% (w/v) of cellulose nanocrystals were incorporated into the PNIPAAm/chitosan matrix to form thermo-responsive injectable composite hydrogels. FT-IR spectra confirmed the successful formation of these hydrogels, highlighting the characteristic peaks PNIPAAm, chitosan and CNCs. The inclusion of CNCs led to a reduced pore size as compared to the control hydrogels. The mechanical properties of the hydrogel were characterized under various temperature conditions. Rheology tests showed that storage modulus (G') increased significantly above 30 °C, indicating gel-like behavior. Thermogravimetric analysis showed thermal stability up to 300 °C. The volume phase transition temperatures (VPTT) of the hydrogels were found to be in the range of 34-38 °C, close to physiological body temperature. The equilibrium swelling ratio (ESR) of the CNC-containing hydrogels was higher than that of the control. In vitro studies with Human Dermal Fibroblast adult (HDFa) cells showed the hydrogels to be non-toxic, suggesting their potential for biomedical applications.

By-product distribution and cytotoxicity assessment of ZnO-assisted photocatalytic degradation of reactive blue 250 dye

This research examined the effectiveness and feasibility of utilizing ultraviolet (UV) assisted photo-catalysis to treat wastewater effluents from textile production containing reactive blue 250 (RB 250) dye. Molecular oxygen and active species like O2•−, HO2•, H2O2 and •OH play crucial roles in the degradation process. Additionally, the degradation of dyes is influenced by several factors, including dye concentration, duration of UV irradiation, pH levels, concentration of H2O2, and the catalyst. The concentration of H2O2 and catalyst dose for the decolorization was studied at 0.6 mL and 0.5 g respectively. The discoloration was higher at low dye concentration, high H2O2 concentration, acidic conditions and high catalyst concentration. The maximum degradation (97 %) of RB 250 dye was obtained in the presence of zinc oxide nanoparticles within 90 min. The extent of decolorization of the dye was determined by UV–Vis spectroscopy. Fourier transform infrared spectroscopy (FTIR) was employed to analyze the changes in functionalities after degradation. The disappearance of characteristic peaks associated with specific groups within the dye molecule confirmed the extensive degradation of RB 250 dye. LCMS analysis was conducted to examine the intermediates and a mechanistic degradation pathway was subsequently proposed. The cytotoxicity of the irradiated dye samples was evaluated through a hemolytic test both pre and post-treatment. The findings suggest that the UV/H2O2/ZnO treatment represents a promising approach for effectively degrading RB 250 dye.

Bile acid conjugated chitosan nanoparticles promote the proliferation and epithelial-mesenchymal transition of hepatocellular carcinoma by regulating the PI3K/Akt/mTOR pathway

Bile acids have been known to play significant roles at certain physiological levels in gastrointestinal metabolism. Yet, they are known to be carcinogenic and aid in tumor progression in most cases, although the roles remain uncertain. Hence, we tested the cytotoxic potential of cholic acid (CA) loaded chitosan nanoparticles (CNPs) on Hep3B cells. The physicochemical properties of the CNPs synthesized with CA load (CA-CNPs) were determined using standard techniques such as ultraviolet–visible spectrophotometry (UV–Vis), fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). The characteristic peak for chitosan nanoparticles were observed for plain CNPs (pCNPs) and CA-CNPs at around 300 nm as per UV–Vis analysis. FTIR analysis indicated the possible trapping of CA onto CNPs as certain peaks were retained and some peaks were shifted. XRD analysis determined that the peaks representing CA and pCNPs were collectively obtained in CA-CNPs. As per DLS analysis, the particle size, PDI and ζ-potential of the CA-CNPs were 259 nm, 0.284 and 30.4 mV. Further, the CA-CNPs were non-cytotoxic on Hep3B cells at the maximum tested concentration of 500 μg/mL. The viability at 500 μg/mL of CA-CNPs was two-fold higher than 500 μg/mL of pCNPs. Also, the pCNPs were not hemolytic and therefore could not have played a role in the increase of viability after treatment with CA-CNPs, which indicates that CA posed a major role in increased viability of Hep3B cells. As per quantitative PCR (qPCR), the upregulated gene expressions of PI3K, Akt, mTORC2, cMyc, Fibronectin, hVPS34, Slug and ZEB1 and the downregulated expression of the tumor suppressor PTEN indicates that PI3K/Akt/mTOR pathway mediated the induction of epithelial-to-mesenchymal transition (EMT) in response to CA-CNPs treatment on Hep3B cells.

Improvement of antibacterial activity of AgNPs@PVA-PVP ternary nanocomposite films followed by gamma-ray irradiation treatment for biomedical applications

Our study investigates the influence of several doses of gamma rays on the antibacterial behavior of nanocomposite of silver nanoparticles (AgNPs) doped in a blend of poly (vinyl alcohol) (PVA)-Polyvinyl Pyrrolidone (PVP). AgNPs@PVA-PVP nanocomposite films were fabricated via laser ablation route, and then the synthesized films were subjected to various gamma ray's doses. X-ray diffraction (XRD) data shows a diffraction peak at 2θ = 38° assigned to the existence of AgNPs. Ultraviolet–visible (UV–Vis) results confirm the characteristic peak of silver nanoparticles at 425 nm. The cell viability and antibacterial behavior results confirmed the enhancement in the performance of AgNPs@PVA-PVP composite after irradiated to gamma rays. These values of cell viability have been raised by increasing the dose of gamma rays to 94.5 ± 6.5 % for dose at 70 kGy gamma rays. The values of the inhibition zone of microorganisms were enhanced by raising the doses of gamma rays to 19.5 ± 0.5 and 21.3 ± 0.6 against E. coli and S. aureus respectively specifically for nanocomposite with gamma dose 70 kGy. Thus, the improved antibacterial activity of AgNPs@PVA-PVP nanocomposite could be used in biomedical applications.

Enhanced Mechanical Properties and Degradation Control of Poly(Lactic) Acid/Hydroxyapatite/Reduced Graphene Oxide Composites for Advanced Bone Tissue Engineering Application.

This study explores the enhancement of poly(lactic acid) (PLA) matrix using calcium hydroxyapatite (cHAP) and reduced graphene oxide (rGO) for developing composite scaffolds aimed at bone regeneration applications. The PLA composites were fabricated through solvent evaporation and melt extrusion and characterized by various techniques, including thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and mechanical testing. The incorporation of cHAP and rGO significantly improved the thermal, mechanical, and morphological properties of the PLA matrix. Mechanical testing revealed that adding 10% cHAP and varying amounts of rGO (0.1%, 0.3%, 0.5%) enhanced tensile and compressive strengths, with the highest improvements observed at 0.5% rGO content. Thermal analysis showed increased thermal stability with higher degradation temperatures for the composites. Spectroscopic analyses confirmed the effective integration of cHAP and rGO into the PLA matrix with characteristic peaks of the fillers identified in the composite spectra. In vitro, degraded action tests in phosphate-buffered saline (PBS) at pH 7.4 over 12 months indicated that composites with higher rGO content exhibited lower mass loss and better mechanical stability. Furthermore, finite element analysis (FEA) simulations were performed to validate the experimental results, demonstrating a strong correlation between simulated and experimental compressive strengths. This novel approach demonstrates the potential of PLA/cHAP/rGO composites in creating effective and biocompatible scaffolds for tissue engineering, providing a comprehensive analysis of the synergistic effects of cHAP and rGO on the PLA matrix and offering a promising material for bone regeneration applications.

Model test study on the dynamic failure process of tunnel surrounding rocks in jointed rock mass under explosive load

The presence of joints can significantly reduce the integrity and stability of an engineering rock mass. Under dynamic loads, such as from blasting excavation, the key blocks divided by joints may be destabilized and prone to sliding, potentially leading to engineering geological disasters like rockbursts. To study the dynamic instability process, similar materials for the rock mass and joints were developed based on the similarity theory, and a tunnel model in the jointed rock mass was constructed. Subsequently, a detonating fuse was used to generate a dynamic load, and the dynamic instability process of the tunnel surrounding rock in the jointed rock mass under explosive load was studied using the geotechnical multifunctional testing device. The deformation characteristics and dynamic instability process of the tunnel surrounding rock were analyzed using acceleration sensors, resistance strain gages, linear variable displacement transducers and motion camera. The study shows that the acceleration at the tunnel vault is significantly greater than at the straight wall and floor under blast loads, with differences reaching an order of magnitude. Acceleration waveforms were classified into three categories based on peak characteristics, explained through the propagation of explosive stress waves. Additionally, strain and displacement at the tunnel arch were also significantly greater than in other areas, indicating more severe stress concentration and dynamic damage at the arch, necessitating reinforced support in tunnel excavation. The entire dynamic instability process of the tunnel surrounding rock was successfully recorded using a motion camera. The dynamic failure process was divided into several phases, the appearance of cracks on the joint surface, particle ejection accompanied by the dropping of jointed blocks, a significant drop of the jointed blocks, and return to calm. The dynamic failure modes include the dropping and rotation of jointed blocks, local particle ejection, and shear cracks on jointed block.

Fe7S8 nanosheets- catalyzed colorimetric and fluorescence dual ratio sensing for high selectivity detection of ascorbic acid

By using Fe7S8 nanosheets (NSs) as catalyst, O-phenylenediamine (OPD) as chromogenic substrate, H2O2 as oxidant, and ascorbic acid (AA) as regulator, a dual ratio colorimetric and fluorescence sensing system for determining AA was constructed. The inherent peroxidase like activity of Fe7S8 NSs enables it to catalyze the oxidation of OPD in the existence of H2O2, resulting in the formation of yellow-colored 2, 3-diaminophenazine (DAP) with a characteristic absorption peak at 450 nm and a fluorescence emission peak at 560 nm. However, the presence of AA could suppress the oxidation of OPD and induce the generation of quinoxaline derivative (QXD) 3-(dihydroxyethyl) furo [3,4-b] quinoxaline-1-one with absorption and fluorescence emission peaks located at 345 and 435 nm, respectively. Thus, employing the absorption of QXD at 345 nm and emission at 435 nm as the reporting signals, and the absorption of DAP at 450 nm and emission at 560 nm as the reference signals, a ratio colorimetric (A345/A450) and ratio fluorescence (F435/F560) dual signal detection method for AA was developed. Under the optimized conditions, the value of A345/A450 was found to be linear with AA concentration in the ranges of 1.0–40 μM and 40–100 μM, and the value of F435/F560 was strongly correlated with AA concentration in the ranges of 1.0–30 μM and 30–100 μM. When applied for the assay of AA in human serum samples, an acceptable recovery ranging from 93.1 to 106.6 % was obtained, confirming the potential of the sensing system in practical applications.

Electrical properties of acetone imprinted hematite nanomaterials doped with Pd & Ag for gas sensing and simulation of their wireless devices

This article presents a novel technique for wireless hydrothermally improved gas sensor devices enhanced by molecular imprinting technique (MIT) for hematite nanomaterials with the existence of acetone using different ratios (10 %, 15 %, and 25 %) as well as doping with palladium/ silver to detect the imprinted gas. α-Fe2O3 are characterized utilizing field emission scanning electron microscope (FESEM), photoluminescence, Fourier transforms infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photo-spectroscopy (XPS), and High-Resolution Transmission Electron Microscopy (HRTEM), Thermogravimetric Analysis (TGA) and utilizes Brunauer-Emmett-Teller (BET) to ascertain their shape, optical properties, and values for surface area and thermal characteristics, respectively. Depending on the preparation conditions, non-regular cubes and rods have typical particle sizes ranging from 25 to 120 nm, acetone imprinted and doped with palladium sample (Ap) offers smaller particles than acetone imprinted sample (A15) making adsorption easier. Where XRD showed all diffraction peaks for α-Fe2O3 as well as XPS authorized the oxidation state, also FTIR showed the characteristic peaks of the stretching mode Fe-O which indicates the formation of α-Fe2O3. Lower defects for (Ap) as it has the highest intensity of 176.15 a.u. in the photoluminescent spectrum, for TGA analysis results explain that pure sample has more thermal stability and lower weight loss. Six hematite films are fabricated using the spin coating technique where acetone molecules are presented during the synthesis process of the nanomaterials to imprint their shapes on the surface of hematite. By measuring the response of the gas sensors and their electrical properties, the I-V curve for Ap showed a rectifying behavior and its shunt resistance (Rsh) is higher than series resistance (Rs) which ensures a high response of (115 %). To develop a wireless gas sensor COMSOL Multiphysics software 5.3(a) software is used for the simulation of three devices model by depositing a layer by specified dimensions of hematites (A15, As, and Ap) with their different electrical conductivities on the surface of rectangular patch antenna by showing geometry, the microstrip patch antenna bandwidth, resonant frequency, scattering parameters, and radiation patterns in the E-plane and 3-D far-field pattern and directivity is calculated also, Sp gives improved reflection coefficient, gain quality factor and directivity due to its high electrical conductivity.

Structural and electrical characterization of nickel sulfide nanoparticles

Nickel sulfide nanoparticles were successfully synthesized through a meticulous process involving a well-mixed powder of Ni(CH3COO)2∙2H2O and Thiourea. The X-ray diffraction analysis provided insights into the structural nature of NiS, revealing its polycrystalline characteristics with a hexagonal system. This information is fundamental, as it forms the basis for understanding the material’s behavior and functionality in various applications. Determining the average values of mean crystallite size, microstrain, and dislocation Nickel sulfide nanoparticles were successfully synthesized through a careful process involving a well-mixed powder of Ni(II)2∙2H2O and Thiourea. The X-ray diffraction analysis provided insights into the structural nature of NiS, revealing its polycrystalline characteristics with a hexagonal system. This information is crucial as it forms the basis for understanding the material’s behavior and functionality in various applications. Determining the average values of mean crystallite size, microstrain, and dislocation density for the (100) plane (32.62 nm, 0.000296, and 0.000939 nm-2, respectively) contributes to a comprehensive understanding of the material’s structural features. The photoluminescence spectrum of NiS in the visible region revealed split peaks at 405.8 and 428.25 nm, shedding light on the radiative recombination process between electrons and holes. The confirmation of thermal stability through a thermogravimetry diagram is essential for applications in elevated temperature environments, ensuring the material’s reliability under varying conditions. Analyzing the stoichiometry of NiS using energy dispersive spectroscopy attached to transmission electron microscopy provides insights into the material’s composition. Cyclic voltammetry results indicating a diffusion coefficient greater than that of NiS added to carbon hold significance for electrochemical applications. The unique characteristic peaks observed in cyclic voltammetry for fuel cell applications suggest the potential use of NiS in energy conversion technologies, broadening its scope of application. The confirmation of NiS’s ability to elucidate the physical and electronic properties of electrochemical systems through electrochemical impedance spectroscopy underlines its importance as a versatile material in various research and practical domains.

Synthesis of biocompatible hydroxyapatite from quail eggshell, oyster shell, and periwinkle snail shell

This study focuses on the synthesis of hydroxyapatite (HA, Ca10(PO4)6(OH)2) from calcium carbonate (CaCO3)-rich quail eggshells, oyster shells, and periwinkle snail shells (Filopaludina bengalensis) through the use of the wet precipitation method. The methodology involved calcining the shell waste to convert CaCO3 to calcium oxide (CaO), undergoing hydration, and reacting with phosphoric acid (H3PO4) to synthesize HA. The results indicated that periwinkle snail shells had the highest percent yield of HA at 92.12%, followed closely by quail eggshells at 92.01%, and oyster shells at 73.65%. For producing CaO, oyster shells provided the highest percent yield of CaO at 103.72%, followed by quail eggshells at 98.6% and periwinkle snail shells at 92.09%. The synthesized HA exhibited high biocompatibility, which is crucial for its potential applications in medical fields such as bone replacement and regeneration. The X-ray diffraction (XRD) analysis confirmed the successful synthesis of high-quality HA, with characteristic peaks indicative of excellent crystallinity and purity and near identicality to the standard XRD pattern of HA of ICDD 9-432 and the XRD pattern of successfully synthesized HA in other studies, indicating high biocompatibility. The research highlights the potential of recycling food waste, specifically shell waste, into valuable biomaterials. This not only addresses environmental concerns but also supports sustainable practices in the food industry. Moreover, the study contributes to advancements in biomaterials for medical applications, emphasizing the viability of utilizing organic waste for high-value products. By transforming food waste into useful medical materials, this research offers promising solutions for waste management and resource utilization, particularly within Thailand's ecological and industrial framework.

Novel CRM cosine similarity mapping strategy for simultaneous in-situ visual profiling lignocellulose in plant cell walls

Confocal Raman microscopy (CRM) is a promising in-situ visual technique that provides detailed insights into multiple lignocellulosic components and structures in plant cell walls at the micro-nano scale. In this study, we propose a novel CRM cosine similarity (CS) mapping strategy for the simultaneous in-situ visual profiling of lignin, cellulose, and hemicellulose in plant cell walls. The main stages of this strategy include: 1) a modified Otsu algorithm for extracting the regions of interest (ROI); 2) a modified subtraction method for cleaning the background signals in the ROI spectra; 3) a lignin signal subtraction method based on the pixel correction factor for eliminating the interference of strong lignin signals with weak cellulose and hemicellulose signals in the Raman full spectra of the cell walls; 4) second-order derivative spectral preprocessing for enhancing the discrimination between the characteristic peaks of cellulose and hemicellulose; 5) a CS mapping algorithm for simultaneous in-situ profiling of lignin, cellulose, and hemicellulose in plant cell walls. The effectiveness of the strategy is verified by characterizing the Brittle Culm1 (BC1) gene-mutant rice stem (IL349-BC1-KO) with known bioinformatics. This approach provides methodological support for in-situ visualization and analysis in fields such as plant or crop science at the micro-nano scale.

Biosorption and transformation of cadmium and lead by Staphylococcus epidermidis AS-1 isolated from industrial effluent.

Rapid utilization of natural resources and other anthropogenic activities intruded heavy metals into the food chain and raised alarming concern for all life forms. The available methods proved insufficient in handling waste and pollutants due to the high cost and generation of toxic residues. Bioremediation strategies have offered sustainable solutions for toxic pollutants. In the current study, cadmium and lead (Cd and Pb respectively) tolerant strains have been isolated from industrial effluent and characterized for tolerance towards target pollutants. The strain was identified by 16s rRNA gene and further used for metal removal from the industrial effluents. Bacterial isolates were obtained from industrial discharge and evaluated for their tolerance towards Cd and Pb. AS-1 bacterial isolate exhibited maximum tolerance towards both the metals and hence was selected for further study. The isolate was identified as Staphylococcus epidermidis. ICP-MS and energy dispersive X-ray (EDX) analysis of biomass revealed that a significant proportion of cadmium (90.89%) and lead (94.87%) available in effluent were sequestered within bacterial biomass. Characteristic peaks at 2Ɵ (31.8637 and 45.6247 for cadmium) and (21.0397, 27.0127, 46.0537, 54.2707 and 75.6547 for lead) confirmed the crystalline nature of the sequestered metals. The selected strain was characterized on biochemical and molecular basis and was found to be Staphylococcus epidermidis. Based on 16S rDNA sequence analysis, a phylogenetic dendrogram was created for the maximum likelihood of the bacterial strain. The sequence was deposited in the NCBI repository (accession number PP587422). The work has shown the possible way out of heavy metal pollution sustainably. To the best of the author's knowledge, this is the first report on the sequestration and reduction of cadmium and lead by a nonpathogenic strain of Staphylococcus epidermidis AS-1 that may be useful for alleviating heavy metal contamination.