Chemical Technique Research Articles

Enhanced gas sensing performance of ZnO and Pt-doped ZnO nanostructured films by chemical spray pyrolysis

This study focuses on the preparation and characterization of zinc oxide (ZO) and platinum-doped zinc oxide (Pt-ZO) nanostructured thin films using the chemical spray pyrolysis technique. Structural and morphological properties of the films were investigated via X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). To understand the semiconducting nature and carrier dynamics, UV-Vis spectroscopy, electrical conductivity measurements, and a static gas sensing system were employed. The films exhibited crystallization in the hexagonal wurtzite structure with a preferred orientation along the (002) plane. FESEM images revealed the presence of small bright particles, particularly abundant in the 5 wt% Pt-doped ZO thin film, indicating the presence of platinum catalysts. Electrical conductivity measurements confirmed the semiconducting nature of the films. Optical parameters such as band gap and absorption index were obtained from UV-Vis spectroscopy. Gas sensing performance towards liquefied petroleum gas (LPG) showed that the 5 wt% Pt-doped ZO thin film exhibited a high response (69.9) to a 50 ppm concentration of LPG at 350 °C. The gas response and recovery times were observed to be 8 s and 12 s, respectively. These results are attributed to interactions between LPG molecules and adsorbed oxygen species on the sensor surface. Platinum atoms on the oxide surface facilitate the formation of oxygen vacancies and the dissociation of oxygen molecules at low temperatures, leading to increased adsorption and reaction with LPG molecules. This results in significant changes in the sensor's resistance, thereby amplifying the sensor response. The findings demonstrate the potential of Pt-doped ZO thin films for practical gas sensing applications.

EUPHORBIA CERIFERA CERA (CANDELILA) EMOLLIENT PROPERTIES, USES AND EFFECTIVENESS IN SKINCARE PRODUCTS

Candelila wax, derived from Euphorbia cerifera cera, is a natural and sustainable component that has a wide range of uses in cosmetic products. This review article explores the chemical composition, extraction techniques, and attributes of Candelila wax, with a focus on its distinctive qualities that make it highly useful in the cosmetic business. Candelila wax has been extensively studied and researched, and these studies have shown that it is highly useful in skincare. It has been found to provide significant benefits in terms of moisturizing the skin, protecting it, and improving the function of the skin barrier. The emollient and moisturizing qualities of this substance enhance skin hydration, while its film-forming capacity creates a protective barrier against environmental stresses. In addition, the non-comedogenic properties and potential anti-inflammatory effects of Candelila wax make it highly suitable for a range of skin types, including those that are sensitive or prone to acne. The future outlook for Candelila wax in cosmetics entails investigating the potential benefits of combining it with other natural substances, creating new and advanced methods of delivering it, and embracing sustainable methods of sourcing and processing. By conducting meticulously planned clinical trials, the effectiveness and safety of the substance may be verified, thereby establishing robust scientific proof for its use in skincare products. By recognizing the possibilities of Candelila wax, we may explore environmentally responsible and skin-conscious cosmetic procedures that align with the changing tastes of mindful customers. By utilizing the potent properties of this natural substance, the cosmetic industry can lead the path towards a more environmentally friendly and enduring future in the field of skincare products.

Uncovering Adrenal Incidentalomas – the role of imaging methods in diagnostic process

Introduction and purpose An adrenal incidentaloma is any lesion found unexpectedly during an imaging study performed for an unrelated reason. The detection rate of incidental adrenal tumors is steadily increasing. The clinical presentation of these tumors is influenced by the specific hormones production, which are determined by their origin. Most lesions are hormonally inactive and may go undetected by physicians, although some can be malignant. The aim of this work is to summarize the utility of different imaging modalities in clinical practice. State of knowledge All adrenal incidentalomas have to undergo an imaging procedure to determine if the mass is homogeneous and lipid-rich and therefore benign or if there are some malignant features. Noncontrast computed tomography is the primary imaging technique used to evaluate adrenal lesions based on their size, structure, and density. It is worth remembering that density <10 HU and homogenous appearance is consistent with a benign adrenal mass and no further imaging is required. When additional diagnostic clarification is needed, especially in malignancy suspicion, magnetic resonance imaging with a chemical shift technique should be conducted and it may be followed by nuclear medicine methods. Conclusions Imaging methods play crucial role in diagnostic process. Imaging studies provide easy follow-ups and allow to avoid unnecessary adrenalectomies and its complications. Therefore, they contribute to optimizing patients’ health management.

Morphological, structural, and electrochemical properties of ZnO- and Ni-doped ZnO nanocrystals formed using different reducing agents in the chemical co-precipitation technique

Morphological, structural, and electrochemical properties of ZnO- and Ni-doped ZnO nanocrystals formed using different reducing agents in the chemical co-precipitation technique

Silver Nanoparticles: A Comprehensive Review of Synthesis Methods and Chemical and Physical Properties.

Recently, silver nanoparticles (NPs) have attracted significant attention for being highly desirable nanomaterials in scientific studies as a result of their extraordinary characteristics. They are widely known as effective antibacterial agents that are capable of targeting a wide range of pathogens. Their distinct optical characteristics, such as their localized surface plasmon resonance, enlarge their utilization, particularly in the fields of biosensing and imaging. Also, the capacity to control their surface charge and modify them using biocompatible substances offers improved durability and specific interactions with biological systems. Due to their exceptional stability and minimal chemical reactivity, silver NPs are highly suitable for a diverse array of biological applications. These NPs are produced through chemical, biological, and physical processes, each of which has distinct advantages and disadvantages. Chemical and physical techniques often encounter issues with complicated purification, reactive substances, and excessive energy usage. However, eco-friendly biological approaches exist, even though they require longer processing times. A key factor affecting the stability, size distribution, and purity of the NPs is the synthesis process selected. This review focuses on how essential it is to choose the appropriate synthesis method in order to optimize the characteristics and use of silver NPs.

Experimental, quantum chemical spectroscopic investigation, topological, molecular docking/dynamics and biological assessment studies of 2,6-Dihydroxy-4-methyl quinoline

The present work is a comprehensive investigation of the spectral, electronic structure, bonding, and reactivity of the 2,6-dihydroxy-4-methylquinoline (26DH4MQ) molecule through a wide range of experimental and quantum chemical spectroscopic calculations techniques, along with its applications as nonlinear optical materials and biological assessments. The study utilized density functional theory (DFT) and time-dependent density functional theory (TD-DFT) with the B3LYP method and the 6-311G++(d,p) basis set to analyze the structural and molecular properties of 26DH4MQ. The findings from UV–Vis, FT-IR, and FT-NMR spectroscopy show a strong agreement between the experimentally obtained vibrational frequencies and chemical shifts and those predicted by computational methods. Local reactivity descriptors, such as the dual descriptor, Fukui functions, and the molecular electrostatic potential (MEP) map, were used to identify the reactive regions of the molecule. Additionally, natural bond orbital (NBO) analysis provided insights into the charge transfer characteristics of 26DH4MQ, which helps to stabilize the molecular system. The study also revealed notable nonlinear optical (NLO) properties, with polarizability (18.52 × 10–24e.s.u.) and first-order hyperpolarizability (2.26 × 10–30e.s.u.) values that surpass those of standard organic compounds, suggesting significant potential for optoelectronic applications. The biological evaluation of 26DH4MQ assessed its drug-likeness, toxicity, enzyme inhibition, and ADME (Absorption, Distribution, Metabolism, and Excretion) parameters, highlighting its pharmaceutical potential. Furthermore, molecular docking and dynamics studies illustrated the compound's interaction with proteins, indicating its potential role as an insulin inhibitor.

Histological and scanning electron microscopy investigation of the effects of titanium surface modifications on osseointegration in rabbits.

This study aimed to compare the novel Estaş Medical Anodization (EMA) surface treatment technique with the techniques commonly used in the literature and to examine their effects on osteointegration in the rabbit tibia. A total of 24 rabbits used in this study were divided into 3 groups, with 8 rabbits in each group. Using both tibias of all rabbits in the study, screws belonging to the control group were placed in the left tibia, and the right tibia belonging to the experimental group were placed. In the first 8 rabbits, a single experimental group in the right tibia were used; in the second 8 rabbits, 2 different experimental groups in the right tibia were used; and in the last 8 rabbits, 2 different experimental groups in the right tibia were used. Thus, 5 different experimental groups with 8 screws in each group and a separate control group were formed for each of them. EMA-treated surfaces were named 200-800 nm iris oxidation and 800-1200 nm gray oxidation according to the TiO2 layer thickness. Group 1 was implanted with mini-screws prepared with chemical etching+EMA iris oxidation, while group 2 was implanted with sandblasted, large-grit and acid-etched (SLA) mini screws treated with EMA gray oxidation. Group 3 was implanted with mini-screws treated with EMA gray oxidation, group 4 was implanted with mini-screws treated with chemical etching+micro-arc oxidation, and group 5 was implanted with mini-screws treated with chemical etching+EMA gray oxidation. The control group was implanted with mini-screws prepared with pure titanium. At the end of 6 weeks, osseointegration percentages were calculated and compared using histological and scanning electron microscope (SEM) analyses. The histological results confirmed the increase in osseointegration percentages in all experimental groups compared to those that received pure titanium implants (P values control group vs group 1=.005, control group vs group 2, 3, 4, 5=.001). The comparison between the groups revealed that the chemical etching+EMA gray oxidation modification technique (group 5) significantly increased osseointegration compared to the SLA+EMA gray oxidation technique (group 5 vs group 2 P=.016) and the chemical etching+EMA iris oxidation technique (group 5 vs group 1 Pp=.001). The EMA gray oxidation technique (group 3) significantly increased osseointegration compared to the chemical etching+EMA iris oxidation technique (group 1) (group 3 vs group 1 P=.043). The results of the SEM analysis showed that osseointegration was significantly increased in all experimental groups compared to that in the pure titanium (control) group (P values control group vs group 1, 2, 3=.001, control group vs Group 4,5=.006). The mean osseointegration percentage in the experimental groups was the highest in group 5, followed by group 4, group 3 and group 1 equally, and group 2. However, the differences among the experimental were not significant (group 1, group 2, group 3, group 4 vs group 5 P=.408). The EMA titanium surface modification techniques we developed significantly increased osseointegration compared to the pure titanium surface. The EMA gray oxidation technique seems to result in higher osseointegration rates than the EMA iris oxidation technique, and similar rates can be found with the SLA and chemical etching techniques. N/A.

Evaluation of analytical uncertainty in quantitative determination of elements - The case of boron

BackgroundThe uncertainty including accuracy and precision is the most vital factor that determines the overall quality of quantitative analysis. The uncertainty has been, however, evaluated relatively within the same analytical technique. Given this background, the present study evaluates the uncertainty on quantitative elemental analysis with a quasi-absolute approach. The objectives of this study are (1) to investigate the analytical uncertainty of prompt gamma-ray analysis (PGA), a chemical interference-free method in principle, on the quantitative analysis of boron and (2) to evaluate the applicability of inductively coupled plasma optical emission spectrometry (ICP-OES), a common technique for quantitative elemental analysis including boron. ResultsPGA provided analytical quantity that is equivalent to the true quantity. The quantity values determined for a series of boron-containing samples are all well above the detection limit of the PGA system, the quantity resolution of which is also much smaller than the minimum difference in quantity among the samples. These facts confirm that the evaluation of analytical uncertainty with the present PGA system is statistically meaningful. The analytical uncertainty in both methods was adequately evaluated by comparing the results from PGA and ICP-OES for a series of boron-containing materials with different physical/chemical properties (i.e. CrB2, B4C, and solidified products of stainless steel-B4C melt) and the major sources of uncertainty in both methods are specified. The conditions for sample preparation/pretreatment were optimized to lower the uncertainty. Significance and noveltyThis study proposes a new concept to perform the quasi-absolute evaluation of analytical uncertainty by employing a chemical interference-free technique. The proposed concept is not limited to the combination of PGA and ICP-OES as demonstrated in this study, but it is applicable to any combination of any analytical methods for any element. Hence, the concept demonstrated in this study could be beneficial to a wide range of analytical chemistry.

Effect of Integrated Weed Management Practices in Rice (Oryza sativa) Under SRI

An experimental study was conducted at the Annamalai University Experimental Farm in Cuddalore District, Tamil Nadu, between February and May 2023. The objective of this work is to chemically manage the developing weeds in rice during vegetative development using the System of Rice Intensification (SRI) technology. Additionally, the study aims to identify the weed flora in the experimental field. In this study, a Randomised Block Design with three replications was employed. The experimental treatments comprised optimal combinations of chemical and mechanical techniques for weed management. The experiment was structured in a randomised block design, consisting of seven treatments, and subsequently reproduced three times. Among the several treatments, the application of Penoxsulam + Butachlor @ 2L/ha (PE) on 3 days after transplantation (DAT) for rice, and the use of Conoweeder twice on 25 and 35 DAT (rice), effectively decreased weed density and thus reduced weed biomass. This led to an improvement in crop development and production. The greater plant height, drying matter potential (DMP), and grain yield seen with the application of Penoxsulam + Butachlor @ 2L/ha (PE) on 3 days after transplantation (DAT), and Conoweeder twice on 25 and 35 DAT, may be attributed to the effective management of a weed-free environment, especially during critical growth phases of the crop. Suppression of agricultural weed competition facilitated increased growth and development of rice crop, resulting in elevated grain and straw yield.

Abstract A056: Pancreatic ductal adenocarcinoma derived cancer-associated fibroblasts suppress tumor infiltrating lymphocytes in the tumor microenvironment

Abstract Patients with pancreatic ductal adenocarcinoma (PDAC) have a poor prognosis due to late presentation of disease and frequent resistance to therapy. Immunotherapy regimens have uniformly failed in PDAC, which has long been considered an immunologically cold tumor. It is believed that immunotherapy has been unsuccessful in PDAC due to its dense, fibrotic, and immunosuppressive microenvironment. Cancer-associated fibrosis may account for up to 90% of the PDAC microenvironment, thus further study of this immunosuppressive component is urgently needed. Methods Human PDAC surgical specimens were procured, sectioned, and allocated for histology, flow cytometry, tumor-infiltrating lymphocyte (TIL) expansion, and fibroblast culture. For histology, tumor slices were saved in 10% formalin and wax embedded. Histological PDAC slides were stained against fibroblasts markers alpha smooth muscle actin, fibroblast activation protein; and T-cell markers CD3, CD69, CD25, FOXP3. First, tumor sections were digested using mechanical and chemical techniques. For flow cytometry, digested tumor cells were stained with fluorescent conjugated antibodies targeting CD45, CD3, CD4, CD8, CD25, CD69, PD-1 and ICAM. For TIL isolation and expansion, resultant single-cells were bead-isolated for CD3 positive cells, cultured and expanded with 2000 IU interleukin-2 and 1.5 mg/mL anti-CD3/CD28 antibodies. For fibroblast culture, fibroblasts were bead isolated and sub-cultured in RPMI supplemented with FGF. TILs were co-cultured with patient-derived fibroblasts/fibroblast media with the PD-L1 inhibitor Atezolizumab. TILs were then analyzed by flowcytometry, and media from co-culture was analyzed via ELISA for gamma interferon release. Results TILs isolated from PDAC (N=5) co-cultured with patient-matched fibroblasts or media were phenotypically compared using flow cytometry and measure for gamma interferon release. Interestingly, TILs co-cultured with fibroblasts or fibroblast media showed improved expansion over peripheral blood derived control T-cells, but both groups showed highly impaired gamma interferon release. Co-cultured TILs had high levels of PD-1 and low levels of CD69, compared to control TILs, indicating a suppressed phenotype. TILs co-cultured with fibroblasts and Atezolizumab resulted in significantly increased CD69 expression and gamma interferon release (P>0.05), indicating an activated phenotype. Histological PDAC slides showed abundant T-cell infiltrates with minimal CD69 expression. CD25+ T-cells were identified throughout fibrotic areas of the TME. Conclusion Here, we challenge the long-held belief that PDAC is immunologically cold as our tumor cross-sections (N=5) were rich in T-cells. More importantly, our results show that tumor-derived fibroblasts appear to play a role in suppression of TIL function, which is partially reversible with immunomodulatory techniques (e.g., anti-PDL1therapy). Our results warrant further investigation into targeting CAFs in PDAC microenvironment to improve patient response to immunotherapy. Citation Format: Charles Bailey, Hannah Mcdonald, Anna Reagan, Michael Cavnar, Mautin Barry-Hundeyin, Prakash Pandalai, Joseph Kim. Pancreatic ductal adenocarcinoma derived cancer-associated fibroblasts suppress tumor infiltrating lymphocytes in the tumor microenvironment [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pancreatic Cancer Research; 2024 Sep 15-18; Boston, MA. Philadelphia (PA): AACR; Cancer Res 2024;84(17 Suppl_2):Abstract nr A056.

Investigating the synergistic effect of Nd3+ and Ni2+ in CuO nanocrystals on their structural, optical, and magnetic properties for photovoltaic and photocatalytic implementations

The wet chemical precipitation technique was used to synthesize CuO, Nd:CuO and Ni-Nd:CuO nanoparticles efficiently. The produced substance was tested using X-ray diffraction (XRD) for confirming the crystallite structure, and scanning electron microscopy (SEM) was used to examine the morphological properties of the produced materials. Crystal defects and optical properties of the synthesized samples were analyzed through luminescence (PL) investigations and UV–Vis spectroscopy. EIS spectrum was utilized to study the electrochemical behavior of the prepared material. Vibrating Sample Magnetometer (VSM) was employed to examine the magnetic properties influencing from the doping of Ni2+ and Nd3+ ions into CuO, attributed to their substantial magnetic moment and ferromagnetic traits. Photovoltaic efficiency of the prepared material was studied by J-V characteristics and photon-to-electron converting efficacy (IPCE) studies. Photocatalytic properties were studied by degrading MB and RhB dyes. The enhancement in the photocatalytic performance of the Ni-Nd:CuO was a result of suppression of photogenerated electron-hole pair recombination and accelerated separation and migration of photogenerated charges.

Real-time SERS sensing of highly toxic seawater contaminants using plasmonic silver assembled pyramidal/nanowire heterostructures

Hierarchically oriented plasmonic nanostructures have attracted an advanced molecular sensing platform for multifaceted applications. In the present work, we have attempted to fabricate ultrasensitive and cost-effective pyramidal/nanowire hetero arrays, hosted with silver nanoparticles for the effective surface-enhanced Raman spectroscopy (SERS) assisted detection of toxic water contaminants. Three-dimensionally oriented pyramidal/nanowire hetero arrays with enhanced surface area were fabricated by combining wet etching and metal-assisted chemical etching techniques. The regulation of structural features was achieved by controlling the process parameters during fabrication. Particularly, the evolution of morphological properties of the hybrid sensor was investigated in terms of nanowire aspect ratio and further analyzed in terms of SERS properties. The hetero arrays exhibited significant enhancement in Raman signal for sensing organic pollutants. Moreover, these hetero arrays with a nanowire length of ∼1 µm exhibited the highest signal enhancement. Further, the excellent reproducibility and reusability characteristics were also demonstrated for the fabricated sensors. Different cationic and anionic organic pollutants were employed for efficacy studies which showed detection limits ranging from femtomolar to picomolar levels. Finally, the real-time sensing of organic contaminants such as aniline was also investigated from seawater with an estimated enhancement factor of 8 × 108, indicating that as-fabricated hetero arrays can perform as outstanding SERS sensors for environmental remediation applications.

Physicochemical, enzymatic and fermentation modifications improve resistant starch levels and prebiotic properties of porang (Amorphophallus oncophyllus) flour

SummaryPorang tubers (Amorphophallus oncophyllus) are one of the Araceae family plants, which naturally contain resistant starch (RS). The RS is able to provide health impacts such as reducing the glycaemic index (GI), preventing the formation of gallstones and cardiovascular disease, and increasing mineral absorption. This research aims to improve the RS and prebiotic properties of porang flour through physical, chemical, enzymatic and microbiological modifications. Research methods include modification with physical treatment of autoclaving‐cooling one and two cycles (AC‐1S and AC‐2S), microwave‐cooling (MWC), heat moisture treatment (HMT), annealing (ANN), chemical treatment with acid hydrolysis (HA), enzymatic treatment with pullulanase debranching (DP) and microbiological treatment with combined heating and cooling fermentation (FAC). The results showed that physical, chemical, enzymatic and fermentation modification techniques increased the characteristics of RS and the prebiotic properties of porang flour. The best modification method for porang flour was obtained in the DP treatment with the morphological characteristics of sharp‐surfaced granules, total starch 39.81%, amylose content 3.73%, amylopectin content 36.08%, reducing sugar content 16.31%, power digestibility 43.81%, very rapidly digestible starch (VRDS) 8.59%, rapidly digestible starch (RDS) 11.08%, slowly digestible starch (SDS) 23.60%, RS 56.73%, resistance to gastric acid 98.60%, lactic acid bacteria (LAB) viability 11.87 log cfu/ml, prebiotic effect 3.07, prebiotic index 2.46 and prebiotic activity 1.77.

Eco-friendly modified chitosan as corrosion inhibitor for carbon steel in acidic medium: Experimental and in-depth theoretical approaches

The industrial and medical sectors have a great interest in chitosan due to its unique properties, such as abundance, renewability, non-toxicity, antibacterial activity, biodegradability, and polyfunctionality. In this work, two modified chitosan Schiff bases (ChSB-1 and ChSB-2) were made using condensation methods, and their potential as corrosion inhibitor for carbon steel in 1 M HCl was investigated using chemical and electrochemical techniques. The ChSB-1 and ChSB-2 inhibitors exhibited remarkable inhibitory performance, as evidenced by the mass loss data, which showed 89.3 % and 91.5 % efficacy at 1 mM concentration, respectively. Because of the electron-donor substituent of methoxy (–OCH3), ChSB-2's active sites have more delocalized electrons than ChSB-1's. The PDP results showed that both ChSB-1 and ChSB-2 inhibitors have anti-corrosion characteristics because heteroatoms caused a protective layer to develop that functioned as mixed-typed inhibitors. The calculated adsorption-free energy ∆Gadso for ChSB-1 and ChSB-2, respectively, was found −36.1 and − 37.1 kJ mol−1. The ChSB-1 and ChSB-2 inhibitors adsorb on carbon steel in acidic conditions through physisorption and chemisorption interactions, and their adsorption is in line with the Langmuir adsorption model. Inhibited and uninhibited metallic surfaces were subjected to surface morphological assessments using contact angle (CA), the scanning electron microscopy and the energy dispersive X-ray (SEM/EDX) analysis. The DMol3 part of Materials Studio 7.0 software was used to perform the quantum chemical calculations based on DFT to visualize the structural features. Studies from quantum chemistry suggest the possibility of surface interaction between the unoccupied orbitals of the metal surface and the inhibitors ChSB-1, ChSB-2, ChSB-1H+, and ChSB-2H+. The results clearly show that the two inhibitors work well as environmentally friendly carbon steel corrosion inhibitors in acidic medium. This could be advantageous for industrial procedures such as pickling, cleaning, acidizing oil drilling in oil wells, and using citrus to de-sediment boilers.

Superior photocatalytic degradation of pharmaceuticals and antimicrobial Features of iron-doped zinc oxide sub-microparticles synthesized via laser-assisted chemical bath technique

Addressing the dual challenges of antimicrobial resistance and pharmaceutical contamination in wastewater is crucial for global health and environmental preservation. Predictions estimate up to 10 million annual deaths by 2050 due to antimicrobial resistance, underscoring the urgent need for innovative solutions. This study explores the potential of zinc oxide Sub-Microparticles (ZnO SMPs) doped with iron (Fe) to enhance the photocatalytic degradation of pharmaceutical compounds in water and improve antimicrobial efficacy. A green laser-assisted chemical bath synthesis method created ZnO SMPs with varying Fe dopant concentrations (1 %, 1.5 %, and 3 %). The synthesized Sub-Microparticles underwent rigorous structural analysis using X-ray diffractometry, SEM, EDX, FTIR, and UV–visible spectrophotometry techniques. Their photocatalytic performance was evaluated in the degradation of paracetamol under blue laser light, and their antimicrobial properties were assessed following CLSI guidelines. Structural analyses confirmed the hexagonal wurtzite structure of ZnO SMPs, with noticeable changes due to Fe doping, including a transition from sub-microrods to sub-microsheets and a redshift in the optical band gap. Photocatalytic tests revealed a significant enhancement in paracetamol degradation efficiency, increasing from 53.41 % with pure ZnO to 98.99 % with 3 % Fe-doped ZnO in 50 min. Antimicrobial assays demonstrated an increased inhibitory effect against pathogens, with Fe-doped ZnO outperforming control discs. This study substantiates the potential of Fe-doped ZnO SMPs in wastewater treatment and antimicrobial applications, showcasing significant improvements in photocatalytic degradation of pharmaceutical compounds and antimicrobial efficacy. The findings underscore the importance of continuing research in this domain for environmental and public health benefits.

Synthesis, optimization, electrochemical and electrochromic properties of Zr-doped NiO films by chemical spray pyrolysis

Zirconium (Zr)-doped NiO films with different contents were successfully synthesized via the chemical spray pyrolysis technique. The structure, morphology, optical and electrochemical behaviors of these films were investigated by X-ray diffraction (XRD), Raman spectrometer, scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), UV–Vis-NIR spectrophotometry, cyclic voltammetry (CV), and chronoamperometry (CA). XRD results suggested that the synthesized samples have the cubic crystal structure and a preferred orientation along the plane (111). Raman spectra further confirmed the successful incorporation of zirconium ions into the NiO films. SEM images explained that the surfaces of the doped films were composed of uniform and dense nanoparticles. EDS analysis suggested that Zr, Ni and O elements were uniformly distributed on the films. The optical results showed that the band gap decreases from 3.53 eV to 3.47 eV as the increase of zirconium doping content. The electrochemical analysis suggested that zirconium doping improved the specific capacitance of the NiO films (the NiO film with the Zr amount of 7 %, 59 F/g at 6 mV/s). In addition, the NiO film with 5 % Zr doped amount exhibited the largest ΔOD (81 %), the largest CE (60.37 cm2/C), and the fastest coloring time (tc =2.1 s) and bleaching time (tb = 2.4 s). These results showed that this film had the excellent electrochromic properties, suggesting that the optimal Zr doped amount of NiO films is 5 %. As a novel kind of electrochromic material, the Zr-doped NiO film has broad application prospects in smart windows, green buildings and energy efficient utilization fields.

Electrocatalytic efficiency of carbon nitride supported gold nanoparticle based sensor for iodide and cysteine detection

Extensive investigations are being conducted on gold nanoparticles focusing on their applications in biosensors, laser phototherapy, targeted drug delivery and bioimaging utilizing advanced detection techniques. In this work, an electrochemical sensor was developed based on graphite carbon nitride supported gold nanoparticles. Carbon nitride supported gold nanoparticles (Au–CN) was synthesized by applying a deposition-precipitation route followed by a chemical reduction technique. The composite system was characterized by X-ray diffraction and X-ray photo electron spectroscopy methods. Electron microscopy analysis confirmed the formation of gold nanoparticles within the size range of 5–15 nm on the carbon nitride support. Carbon nitride supported gold based sensor was employed for the electrochemical detection of iodide ion and l-cysteine. The limit of detection and sensitivity of the sensor was attained 8.9 μM and 0.96 μAμM⁻1cm⁻2, respectively, for iodide ion, while 0.48 μM and 5.8 μAμM⁻1cm⁻2, respectively, was achieved for the recognition of cysteine. Furthermore, a paper-based electrochemical device was developed using the Au–CN hybrid system that exhibited promising results in detecting iodide ions, highlighting its potential for economic and portable device applications.

Highly Active Cerium Oxide Supported Solution Combustion Cu/Mn Catalysts for CO-PrOx in a Hydrogen-Rich Stream

Mono- and di-substituted cerium oxide catalysts, viz. Ce0.95Cu0.05O2-δ, Ce0.90Cu0.10O2-δ, Ce0.90 Cu0.05Mn0.05O2-δ, Ce0.85Cu0.10Mn0.05O2-δ, and Ce0.80Cu0.10Mn0.10O2-δ, were synthesized via a one-step urea-assisted solution combustion method. The elemental composition and textural and structural properties of the catalysts were determined by various physical, electronic, and chemical characterization techniques. Hydrogen temperature-programmed reduction showed that co-doping of copper and manganese ions into the CeO2-δ lattice improved the reducibility of copper. Powder XRD, XPS, HR-TEM, and Raman spectroscopy showed that the catalysts were a singled-phased, solid-solution metal oxide with a cerium oxide cubic fluorite (cerianite) structure, and evidence of oxygen vacancies was observed. Catalytic results in the preferential oxidation of CO in a hydrogen-rich stream showed that complete CO conversion occurred between 150 and 180 °C. Furthermore, at 150 °C, Ce0.90Cu0.05Mn0.05O2-δ, Ce0.90 Cu0.10O2-δ, and Ce0.85Cu0.10Mn0.05O2-δ catalysts were the most active, achieving complete CO conversion and CO2 selectivity of 81, 79, and 71%, respectively. The catalysts performed moderately in the presence of CO2 and water, with the Ce0.90Cu0.05Mn0.05O2-δ catalyst giving a CO conversion of 80% in CO2, which decreased to about 60% when water was added.

Producing Freestanding Single-Crystal BaTiO3 Films through Full-Solution Deposition.

Strontium aluminate, with suitable lattice parameters and environmentally friendly water solubility, has been strongly sought for use as a sacrificial layer in the preparation of freestanding perovskite oxide thin films in recent years. However, due to this material's inherent water solubility, the methods used for the preparation of epitaxial films have mainly been limited to high-vacuum techniques, which greatly limits these films' development. In this study, we prepared freestanding single-crystal perovskite oxide thin films on strontium aluminate using a simple, easy-to-develop, and low-cost chemical full-solution deposition technique. We demonstrate that a reasonable choice of solvent molecules can effectively reduce the damage to the strontium aluminate layer, allowing successful epitaxy of perovskite oxide thin films, such as 2-methoxyethanol and acetic acid. Molecular dynamics simulations further demonstrated that this is because of their stronger adsorption capacity on the strontium aluminate surface, which enables them to form an effective protective layer to inhibit the hydration reaction of strontium aluminate. Moreover, the freestanding film can still maintain stable ferroelectricity after release from the substrate, which provides an idea for the development of single-crystal perovskite oxide films and creates an opportunity for their development in the field of flexible electronic devices.

Microwave digestion method for sulfide analysis of Çanakkale region coal

ABSTRACT Quantitative analysis of sulfide content in coal is a necessary step for complete analysis. Conventional analysis methods take several days, whereas it takes a few hours in microwave digestion method. In the present study, a new wet chemical analysis technique was developed and applied to quantify the sulfide content in Turkish coal samples. In the initial step, 5 M HCl solution is employed to dissolve the sulfate phases present in the coal. Subsequently, pyrite is separated from the residue obtained in stage 1 through the utilization of 2 M HNO3 solution. The final stage involves the determination of organic sulfur, wherein concentrated HNO3, HCl, HF, and boric acid are utilized to completely decompose the remaining residue from stage 2. The extracted solutions from each stage are promptly analyzed for sulfur content using ICP-OES. The cumulative values of the three sulfur forms consistently correspond with certified total sulfur data for the majority of the examined coals. Among several advantages, the analysis duration is the most distinctive feature. Chemical analysis of sulfide in coal with microwave analysis method completed three times rapid than with conventional analysis.