One-Pot Transformation of (R)-(+)-Citronellal over a Bifunctional Ni/ZnBr2/β-Zeolite Catalyst

The distribution of arsenic (As) and cadmium (Cd) in himematsutake was analyzed using scanning electron microscopy-energy dispersive X-ray spectrometer (SEM-EDX). The atomic percentage of the metals was confirmed by inductively coupled plasma-mass spectrometer (ICP-MS). Results show that the accumulation of As in pileus was higher than that in stipe by both SEM-EDX and ICP-MS analyses. The Cd level in pileus was higher than that in stipe by SEM-EDX analysis; whereas a higher level of Cd was found in stipe by ICP-MS analysis. Results of regression analysis showed that there was a positive correlation between the content of As and Cd in the piece samples by both SEM-EDX and ICP-MS methods. Results suggest that the SEM-EDX is one of the potential tools for rapid detection of metals, namely, As and Cd in himematsutake. Key words: Arsenic (As), cadmium (Cd), scanning electron microscopy-energy dispersive X-ray spectrometer (SEM-EDX), coupled plasma-mass spectrometer (ICP-MS), himematsutake.

Electrochemical degradation using seawater and graphite electrodes from waste batteries for methylene orange (MO) dye degradation has been successfully carried out. Electrode characterization, electrolyte calibration, and dye degradation effectiveness with various voltages, pH, kinetics, and degradation reaction mechanisms were observed. Characterization showed a characteristic 2θ peak by X-ray diffractometer (XRD) at 26.5 °, and scanning electron microscopy-energy dispersive X-ray spectrometer (SEM-EDX) showed the morphology of hollow grains with carbon (C) and oxygen (O) composition. In addition, scanning potentiometry showed the initiation of hypochlorite compound formation and MO degradation. Further study of degradation effectiveness showed optimal results at 3 volts and above voltages. Hypochlorous acid (HOCl) and hypochlorite ions (OCl-) from seawater are very effective oxidizing agents in acidic conditions compared to other pH conditions. Pseudo-first-order kinetics regulate the electron attack from the hypochlorite oxidizer (OCl-), the hydroxyl groups (•OH) from the seawater electrolysis mechanism with graphite electrode media on the reactive groups, the ring binding on MO, and the degradation. This indicates that the graphite electrode system used to reuse waste batteries and seawater has the potential to degrade waste dyes in aquatic environments. HIGHLIGHTS Electrochemical system with graphite electrode battery waste and seawater electrolyte. Characterization with XRD, SEM-EDX, spectrometry, and potentiometry. Analysis of the effect of voltage and pH treatment variation. Kinetic and degradation mechanism of methylene orange. GRAPHICAL ABSTRACT

This research aims to investigate the effect of various amount of Ni metal which is impregnated on Mordenitetoward the catalytic activity of the Cashew Nut Shell Liquid Oil (CNSLO) hydrotreating process. The Ni/Mordenitecatalysts were prepared by wet impregnation method using Ni(NO3)2ꞏ6H2O with the Ni content varied under 1, 3, 5wt.% and mordenite which were dissolved in methanol and carried out drying, calcination, and reduction.Hydrotreating is carried out in a semi-batch stainless steel reactor which is flowed with H2 gas. The catalyst wascharacterized and analyzed by Fourier Transform Infrared, X-Ray Diffractometer, Scanning Electron Microscope-Energy Dispersive X-Ray Spectrometer, Transmission Electron Microscopy, Gas Sorption Analyzer, and AtomicAbsorption Spectrophotometer. The total acid amount test was carried out using ammonia vapor adsorption with thegravimetric method. The liquid product of hydrotreating was analyzed by Gas Chromatography-Mass Spectroscopy.Increasing the amount of metal impregnated on mordenite will increase the total acid site, activity, and selectivity ofthe gasoline fraction.

One of the calcium phosphate compounds that can be used as an antibacterial material for coating dental implants is fluorapatite (FAp). This research aims to synthesize FAp at three different sintering temperatures (600, 800, and 1000°C), copper(II) oxide (CuO), and fluorapatite-copper(II) oxide (FAp-CuO) using the sol-gel method, and test the antibacterial properties of the synthesized products. The sol-gel technique proved successful in synthesizing FAp, with optimal results observed at a sintering temperature of 1000°C, achieving a crystallinity level of 90%. Analyses conducted using X-ray diffractometer, Fourier-transform infrared spectrometer, and scanning electron microscope-energy dispersive X-ray spectrometer revealed FAp as the dominating phase, exhibiting Ca/P and P/F ratios of 1.84 and 4.67, respectively. In FAp-CuO, replacing Ca2+ with Cu2+ ions lowered the average crystallite size, crystallinity, and Ca/P ratio. FAp, CuO, and FAp-CuO all displayed antibacterial activities against S. aureus and E. coli, with FAp-CuO having the maximum average inhibitory zone diameters of 0.243 and 1.397 mm, respectively.

This research aims to investigate the effect of various amount of Ni metal which is impregnated on Mordenitetoward the catalytic activity of the Cashew Nut Shell Liquid Oil (CNSLO) hydrotreating process. The Ni/Mordenitecatalysts were prepared by wet impregnation method using Ni(NO3)2ꞏ6H2O with the Ni content varied under 1, 3, 5wt.% and mordenite which were dissolved in methanol and carried out drying, calcination, and reduction.Hydrotreating is carried out in a semi-batch stainless steel reactor which is flowed with H2 gas. The catalyst wascharacterized and analyzed by Fourier Transform Infrared, X-Ray Diffractometer, Scanning Electron Microscope-Energy Dispersive X-Ray Spectrometer, Transmission Electron Microscopy, Gas Sorption Analyzer, and AtomicAbsorption Spectrophotometer. The total acid amount test was carried out using ammonia vapor adsorption with thegravimetric method. The liquid product of hydrotreating was analyzed by Gas Chromatography-Mass Spectroscopy.Increasing the amount of metal impregnated on mordenite will increase the total acid site, activity, and selectivity ofthe gasoline fraction.

Boron reduces aluminum deposition in alkali-soluble pectin and cytoplasm to release aluminum toxicity

Decrease in the organic content of refinery wastewater by photocatalytic Fenton oxidation using iron-doped zeolite: Catalyst preparation, characterization, and performance

Dental implants play an important role in oral health. Titanium dental implants must endure the complex microflora environment of the oral cavity. Moreover, bacterial infections have been considered as one of the most important factors of implant failure. The issue of dental improvement through modification of chemical composition and surface treatment has received considerable critical attention. γ-TiAl as a novo biocompatible material revealed a slower corrosion rate in biological media rather Ti-6Al-4V. The objective of this study is to investigate the effect of Er,Cr:YSGG laser on γ-TiAl in comparison with sandblasted and acid-etched samples as the control groups and machined samples.Wettability, surface roughness, surface topography, scanning electron microscopy-energy dispersive X-ray spectrometer analysis of surface and subsurface of samples were investigated and bacteria counts of two periodontal bacterial strains (Aggregatibacter actinomycetemcomitans and Eikenella corrodens) were evaluated on the Er,Cr:YSGG laser surface-treated sandblasted and acid-etched and machined samples.The results of this investigation show that Er,Cr:YSGG laser surface treatment affects surface roughness, surface topography, wettability, chemical composition of the surface and bacteria count. Scanning electron microscopy-energy dispersive X-ray spectrometer analysis of the sample revealed the increment of titanium and oxygen content and reduction of aluminum content in the surface and subsurface layer. A. actinomycetemcomitans and E. corrodens count were found from the lowest level to highest in the sandblasted and acid-etched samples, laser samples and machined samples, respectively.Using controlled parameters of Er,Cr:YSGG laser ensured no significant adverse alteration. The findings to emerge from this study revealed the significant correlation between microbial count and wettability. Furthermore, the contact angle strongly correlated with surface roughness.

Gunshot residue (GSR) is a composite of unburnt and partially burnt particles from various components of firearm ammunition cartridges. GSR is customarily sampled from small, localized spots and analyzed visually and elementally. The conventional analytical methods for localized GSR are most commonly done through a paired scanning electron microscope-energy dispersive X-ray spectrometer (SEM-EDS) to look for the presence of lead, barium, and antimony, the inorganic components of ammunition primer. Previous GSR analysis primarily focused on the material deposited on a shooter's hands and used swabbing or adhesive stubs to collect GSR. In this study, total gunshot residue (tGSR) from six types of ammunition was collected from fabric that was shot at a muzzle-to-target distance of 15cm. Subsequently, each tGSR sample was digested in nitric acid and analyzed with total reflection X-ray fluorescence spectrometry (TXRF). The TXRF technique can simultaneously identify the individual elements in the tGSR and provide absolute elemental quantification. In contrast, EDS scans report the relative elemental compositions of localized GSR samples rather than giving absolute quantitation. This study reliably revealed distinct patterns in six key elements (lead, copper, barium, antimony, iron, and zinc) of tGSR among the ammunition investigated. Elemental profiles were developed from the analyses to represent each ammunition type and the elemental quantities obtained could be used to suggest the category of ammunition that was used.

Paint types on black-on-white pottery in the prehistoric American Southwest have had significance for both chronological and sociocultural interpretations. Visual attributes have formed the basis for distinguishing carbon- and mineral-based paints on ancient black-on-white pottery in the American Southwest for over 60 years. In this study, an SEM-EDS (scanning electron microscope-energy dispersive X-ray spectrometer) system was first used to make an independent objective determination of the mineral or non-mineral paint present on 15 Mesa Verde White Ware sherds. Then, a group of 19 people (including experienced archaeologists and newly trained individuals) examined and classified the paint on these sherds, achieving an overall accuracy of 84.2 percent. This group also ranked in priority order the visual attributes they felt were most useful in determining pottery paint type: nature of edges (fuzzy, sharp), absorption (soaks in, sits on top), luster (shiny, dull), color range (black-gray-blue; black-brown-reddish), flakiness (doesn't flake off, flakes off), thickness (thin, thick), and surface polish (polish striations visible through paint, striations not visible through paint). In each case, the attribute applicable to carbon-based paint is listed first. The most difficult sherds for the group to identify displayed attributes of both carbon and mineral paints. A category for "mixed" paint type, already in use by archaeologists, is a reasonable third category for labeling sherd paint, as long as it does not become a "catch-all" category. For problematic sherds, the SEM-EDS can be used to characterize paint type, then the visual attributes adjusted to improve investigator accuracy in paint type determination.

This paper examines the knives of the medieval period (13th -14th century AD) from Kinet Höyük in Cilicia, one of the most important areas of Anatolia for the history of iron production. The materials and production processes of 12 knives were revealed using archaeometry methods, such as Optical Microscopy (OM), Scanning Electron Microscope-Energy Dispersive X-Ray Spectrometer (SEM-EDS) analyses, and micro-hardness tests. An examination of the relationship between the shape and size of these knives was undertaken, along with a discussion of the factors involved in the manufacturing techniques. Among the medieval knives from Kinet Höyük that were analyzed, the results of the study indicate that besides blades made entirely of steel or wrought iron there are examples of forge-welding steel to wrought iron in a variety of ways. The largest group of knives is composed of small blades made only of steel. A particular example of this group is a blade made of crucible steel, which was skillfully forged and heat-treated. The medieval blades from Kinet Höyük exhibit a direct relationship between their shapes and their dimensional proportions. A specific production method, however, seems not to have been chosen in accordance with a given shape. The dimensions of the knives were more significant, particularly when only steel or only wrought iron was used. Based on the historical iron-producing activities in the region and the traces of intense blacksmithing practices found in the medieval layers of Kinet Höyük, it is argued that these knives are remnants of a skilled metal production culture.

The synthesis of Ce/mesoporous silica (Ce/MS) and its lifetime determination for the hydrocracking of waste lubricant has been carried out. The MS was synthesized using tetraethyl orthosilicate (TEOS) and gelatin extracted from bovine bone as a template. Cerium was impregnated onto the MS by wet impregnation method using Ce(NO3)3.6H2O. The MS and Ce/MS were then characterized by means of acidity using ammonia base vapor adsorption, Fourier Transform Spectrophotometer (FTIR), Transmission Electron Microscope (TEM), Scanning Electron Microscope-Energy Dispersive X-ray Spectrometer (SEM-EDX), and surface area analyzer (SAA) based on the BET and BJH equation. The Ce/MS catalyst was tested in hydrocracking of waste lubricant in three runs. Lifetime of Ce/MS catalyst was determined using a linear regression of the liquid product yields vs hydrocracking time. The Ce/MS catalyst showed an acidity of 2.79 mmol/g, BJH desorption pore diameter of 3.84 nm, BET surface area of 246.55 m2/g, and total pore volume of 0.44 cm3/g. The yield of liquid product obtained from hydrocracking of waste lubricant using the Ce/MS catalyst for the first, second, and third runs was 21.42, 17.23 and 10.54 wt.%, respectively for 2.5 h per each run. Lifetime of Ce/MS catalyst in hydrocracking of waste lubricant was 12.54 h.

Molar-incisor malformation (MIM) is a new type of root anomaly reported recently. The characteristics of MIM are dysplastic root formations, constriction of pulp chambers and presence of calcified matrices at the level of cementoenamel junction in permanent first molars and primary second molars. In some cases, permanent maxillary incisors are also affected.The permanent first molars of the patient in this case report were affected with MIM. Generalized pulp stones were observed in overall primary dentition. Micro-computed tomography (micro-CT) imaging and scanning electron microscope-energy dispersive X-ray spectrometer analysis were performed on the extracted mandibular first molar and maxillary primary second molar of the patient. Micro-CT images revealed the discontinuity of enamel directly connected to an accessory canal of the root.

This study investigates the dissolution behavior of oxide layers containing radionuclides using perfluorocarbon (PFC) emulsion as a reusable medium. Chemicals such as PFC, anionic surfactant, and H2SO4 are used for preparing the PFC emulsion, and emulsified using an ultrasonication process. The FTIR results show O–H stretching that is formed by the interaction of the carboxyl group of the anionic surfactant with the hydroxyl group of water containing H2SO4, and find that the H2SO4 can be homogeneously dispersed in the PFC–anionic surfactant–H2SO4 emulsion. The dissolution test of the simulated Cr2O3 specimen is conducted using PFC emulsion containing KMnO4. Through the weight losses of specimens and Scanning Electron Microscope-Energy Dispersive X-ray Spectrometer (SEM-EDS) analysis, it is confirmed that the Cr2O3 layer on the SUS304 specimen is easily dissolved using PFC emulsion. During the dissolution of the Cr2O3, it is observed that the dispersed H2SO4–KMnO4 became unstable and separated from PFC emulsion. Based on these results, the behavior of the PFC emulsion during the dissolution of the oxide layer is explained.

Reduction of silver ions to silver nanoparticles by biomass and biochar: Mechanisms and critical factors