Primary Ion Research Articles

CLOUDY modeling suggests a diversity of ionization mechanisms for diffuse extraplanar gas

Context. The ionization of diffuse gas located far above the energetic midplane OB stars poses a challenge to the commonly accepted notion that radiation from OB stars is the primary ionization source for gas in galaxies. Aims. We investigated the sources of ionizing radiation, specifically leaking midplane H II regions and/or in situ hot low-mass evolved stars (HOLMES), in extraplanar diffuse ionized gas (eDIG) in a sample of eight nearby (17−52 Mpc) edge-on disk galaxies observed with the Multi Unit Spectroscopic Explorer (MUSE). Methods. We constructed a model for the photoionization of eDIG clouds and the propagation of ionizing radiation through the eDIG using subsequent runs of CLOUDY photoionization code. Our model includes radiation originating both from midplane OB stars and in situ evolved stars and its dilution and processing as it propagates in the eDIG. Results. We fit the model to the data using the vertical line ratio profiles of our sample galaxies, and find that while the ionization by in situ evolved stars is insignificant for most of the galaxies in our sample, it may be able to explain the enhanced high-ionization lines in the eDIG of the green valley galaxy ESO 544−27. Conclusions. Our results show that while leaking radiation from midplane H II regions is the primary ionization source for eDIG, in situ evolved stars can play a significant part in ionizing extraplanar gas in galaxies with low star forming rates.

Defining Cardiomyocyte Repolarization Response to Pharmacotherapy in Long-QT Syndrome Type 3.

Long-QT syndrome is a primary cardiac ion channelopathy predisposing a patient to ventricular arrhythmia through delayed repolarization on the resting ECG. We aimed to establish a patient-specific, human induced pluripotent stem cell (hiPSC)-derived cardiomyocytes model of long-QT syndrome type 3 (LQT3) using clustered regularly interspaced palindromic repeats (CRISPR/Cas9), for disease modeling and drug challenge. HiPSCswere generated from a patient with LQT3 harboring an SCN5A pathogenic variant (c.1231G>A; p.Val411Met), and an unrelated healthy control. The same SCN5A pathogenic variant was engineered into the background healthy control hiPSCs via CRISPR/Cas9gene editing to generate a second disease model of LQT3 for comparison with an isogenic control. All 3 hiPSC lines were differentiated into cardiomyocytes. Both the patient-derived LQT3 (SCN5A+/-) and genetically engineered LQT3 (SCN5A+/-) hiPSC-derived cardiomyocytesshowed significantly prolonged cardiomyocyte repolarization compared with the healthy control. Mexiletine, a cardiac voltage-gated sodium channel (NaV1.5) blocker, shortened repolarization in both patient-derived LQT3 and geneticallyengineered LQT3 hiPSC-derived cardiomyocytes, but had no effect in the control. Notably, calcium channel blockers nifedipine and verapamil showed a dose-dependent shortening of repolarization, rescuing the phenotype. Additionally, therapeutic drugs known to prolong the corrected QT in humans (ondansetron, clarithromycin, and sotalol) demonstrated this effect invitro, but the LQT3 clones were not more disproportionately affected compared with the control. We demonstrated that patient-derived and genetically engineered LQT3 hiPSC-derived cardiomyocytesfaithfully recapitulate pathologic characteristics of LQT3. The clinical significance of such an invitro model is in the exploration of novel therapeutic strategies, stratifying drug adverse reaction risk and potentially facilitating a more targeted, patient-specific approach in high-risk patients with LQT3.

Assessing drinking water quality in Eloued, south-East Algeria, using the groundwater pollution index (GPI) and the synthetic pollution index (SPI) model.

Groundwater quality degradation is a significant environmental issue worldwide, with potentially severe economic consequences and harm to ecosystems and biodiversity. This can directly affect human health, particularly in developing countries where rapid and uncontrolled urbanization is on the rise. Groundwater is the primary resource for meeting the water needs of the Eloued region, located in southeastern Algeria. Water is considered unfit for human consumption if its physico-chemical elements exceed national or international standards or guidelines. We used the GPI and SPI indices to evaluate the quality of groundwater suited for drinking. Groundwater samples were obtained from 22 wells at depths of more than 250m. Standard analytical procedures were used to determine the physicochemical characteristics of the collected samples, which included pH, EC, TDS, Na+, Ca+2, Mg+2, K+, Cl-, HCO3-, SO4-2, NO3-, NO2-, NH4+ and PO4-3. Multivariate statistical analysis and GIS techniques were used to process the results. The results of the selected physicochemical parameters were compared with World Health Organization (WHO) guidelines to determine the quality of drinking water. The findings indicate that the waters of the terminal complex aquifer are salty and contain medium to high quantities of main ions that surpass the established drinking water limits. The primary ions' relative abundance is Cl- > SO4-2 > HCO3- > NO3 for anions and Na+ > Ca+2 > Mg+2 > K+ for cations. Groundwater chemical types were dominated by Na+, Ca+2, Cl-, and SO4-2. Principal Component Analysis (PCA) showed that alteration and dissolution of carbonates, evaporates, salts, partly silicates, and evaporation, are the main reasons affecting the chemical composition of water in Eloued. The GPI results show that 18.18%, 54.54%, and 27.27% of the water samples were classed as lightly polluted, moderately polluted, or substantially polluted for drinking purposes, respectively. According to the SPI study, 9.09%, 36.36%, 36.36%, and 18.18% were considered drinkable, mildly contaminated, moderately polluted, and seriously polluted for drinking purposes, respectively. According to the GPI and SPI models' geographical distribution maps, potable water is generally scarce and concentrated in the northeastern section of the research area, near the town of Ourmes.

Development and characterization of zinc ion conducting biopolymer electrolytes based on cellulose acetate for primary zinc ion batteries

Development and characterization of zinc ion conducting biopolymer electrolytes based on cellulose acetate for primary zinc ion batteries

Mechanisms of muscle tissue adaptation in response to the influence of low-dose ionizing radiation

Mechanisms of interaction of ionizing radiation with biological objects are a chain of successive physical and physico-chemical changes, which manifest themselves in the form of excitation, primary and secondary ionization of molecules. Biosynthesis of ATP, which is carried out by a system of oxidation-reduction enzymes localized in the inner membrane of mitochondria - the respiratory chain, belongs to the vital processes that are directly disturbed under the action of ionizing radiation. The high degree of damage to this system is due to the significant radiosensitivity of metal-containing enzymes. The purpose of the work is to study the formation of the adaptive response of muscle tissue of sexually mature rats to the influence of ionizing radiation at a dose of 0.5 Gy. It was concluded that a day after irradiation with the dose of 0.5 Gy, the content of contractile proteins in skeletal muscle decreases slightly. On the 15th day, the content of contractile proteins began to decrease. By the 30th day, the content of contractile proteins decreased by 22.9% for myosin, by more than 11% for actin, and by 7 and 8% for troponin and tropomyosin, respectively, compared to the values of the intact group. A similar picture is observed in the cardiac muscle. Mg2+,Ca2+-ATP-ase activity of actomyosin, starting from the 1st day was shown to be increased in both the skeletal and cardiac muscles, reaching its peak in the cardiac muscle on the 15th day, in contrast to the skeletal muscle, where this indicator reached its peak on the 7th day. The authors conclude that irradiation of sexually mature animals with the dose of 0.5 Gy forms an adaptive response that is accompanied by an increase in Mg2+,Ca2+-ATP-ase activity due to the formation of a strong form of binding between F-actin and myosin, actin monomers go into the typical for actomyosin “turned on stage”, and the myosin heads acquire an ordered orientation in the muscle fiber. According to author’s idea, the data obtained indicated the benefit and reasonability of using in post-radiation dysfunctions complex pharmacological treatment drugs that are able to normalize intracellular homeostasis, eliminate probable acidic changes initiated by radiation exposure, activate the processes of intramuscle energy generation and which have protective properties in relation to the muscular system.

Beyond Artists' Colors: A Spectral Reference Database for the Identification of β-Naphthol and Triarylcarbonium Colorants by MeVSIMS.

β-Naphthol and triarylcarbonium colorants were often used by modern and contemporary artists in materials such as inks and paints. Their poor stability and ability to fade upon exposure to light make their identification in artworks crucial for planning exhibitions and preventive conservation. Secondary ion mass spectrometry with MeV primary ions (MeV SIMS) is necessary when analyzing synthetic organic colorants (SOCs) with similar molecular structures due to its advantages in high sensitivity and soft ionization, which causes a low fragmentation of organic molecules. In this work, we applied MeV SIMS with 5 MeV Si4+ to identify selected β-naphthol and triarylcarbonium colorants from the 19th/20th century Materials Collection kept at the Academy of Fine Arts Vienna. The collection contains SOCs from renowned companies, such as I.G. Farben and I.C.I., and serves as a unique source of reference materials in the analysis of artworks. Previous research on these colorants with X-ray fluorescence analysis (XRF), micro-Raman, and Fourier transform infrared (FTIR) spectroscopies failed in the case of colorant mixtures. Similar spectral features of the SOCs within one chemical class and their low concentrations in mixtures did not lead to their identification using these techniques. MeV SIMS detected molecular ions or protonated molecules in the positive-ion mode. In the negative-ion mode, the functional groups (NO2 - and SO3 -) of β-naphthol lakes/pigments and heteropolyacid species (WO3 - and MoO3 -) characteristic of triarylcarbonium toners were determined. The results demonstrate that MeV SIMS is highly effective for identifying β-naphthol and triarylcarbonium colorants in mixtures and distinguishing between pigments, toners, lakes, and dyes.

Evaluation of the detector linearity response of the DR system in different x-ray bean filters

In the recent past, at Brazilian radiology services, direct digital radiography (DR) systems are replacing Computed Radiography (CR). This situation provides several significant advantages such as improving digital image quality, patient effective dose reduction, and improved speed of examinations performed. To evaluate DR systems, various organizations have published protocols with guidelines concerning quality assurance and acceptance tests for DRs. In these protocols, there are methodologies for evaluating several parameters, such as the detector linearity response (DLR). To test the DLR, different methodologies are proposed by the organizations, such as the application of different additional filters on the X-ray beams spectrum to promote the X-ray doses suitable to produce the latent image in the DR. The objective of this work was to evaluate the results of different protocol methodologies for carrying out the DLR test of a DR flat panel. An analogic radiology equipment, a primary ionization chamber, a DR system and images unprocessed were used in this study. As indicated by the protocols, the spectra of the X-rays were modified by additional filters of copper (Cu) with aluminum (Al); Al; Cu; and polymethylmethacrylate (PMMA). The spectra of the X-rays were modified to achieve the exposure range of 0.1 to 7 mR. The results showed that the DLR curves adjustment were R²>0.99, for a logarithmic equation, type y=a.ln(x)+b. For the filters of 0.5 mmCu with 1.0 mmAl; 11.5 mmAl; 1.0 mmCu; 21 mmAl the mean pixel values showed 0.9% of the coefficient of variation (COV), while for 10 cm PMMA filters, the COV increased to 2.7%. The study showed that methodologies using Al, Cu and Al with Cu filters DLR have similar responses while using PMMA, the response was slightly different.

Conceptual design of sandwich walls for shielding against secondary neutrons using MC simulations with FLUKA

FLUKA Monte-Carlo transport code was employed to evaluate the secondary neutron spectra emerging from spherical sandwich shielding configurations composed of concrete and soil, similar to that used at the particle therapy facility MedAustron. This study provides a comparative analysis of neutron spectra attenuated by a concrete-soil-concrete (CSC) sandwich wall shielding configuration versus a full concrete wall design (CCC). Furthermore, we enhanced the shielding performance of the CSC configuration by adding an additional concrete layer (CCSC) to achieve results comparable to the CCC shielding. Two scenarios were tested for shielding performance: (1) primary protons at 100 MeV, and (2) primary carbon ions (C-ions) at 190 MeV/u. Our simulations with primary protons of 100 MeV showed that adding additional internal concrete wall to the CSC configuration, therefore designing the CCSC configuration, the RP performance becomes slightly improved – the HE-peak drops from (1.43 ± 0.11)10−11 to (5.62 ± 0.3)10−12, about 2.5 times. Still, the HE-peak of the exiting neutron spectrum from CCC -(6.29 ± 1.87) 10−13 is about 9 times lower than that exiting CCSC - (5.62 ± 0.3) 10−12.Our simulations with primary C-ions showed that by placing an additional internal concrete wall to the CSC configuration (CCSC) the RP performance becomes slightly improved – the exiting HE peak can be further attenuated from (6.92 ± 0.40)10−9 for CSC to (3.79 ± 0.15)10−9, becoming comparable to the one exiting the CCC configuration, (0.92 ± 0.04)10−9, only 4 times higher. Future research should be focused on improvements of the RP performance of the CCSC, by increasing the soil layer thickness and taking into consideration the humidity (water content) in the soil and concrete and also improve the number of primaries to 109 or even 1010 for better statistical outcome.

Designing new sulfate ionophores for potentiometric membrane sensors: Selectivity assessment and practical application

Developing potentiometric chemical sensors for sulfate determination is a rather challenging task due to a considerable hydrophilicity of this anion and its poor affinity to lipophilic plasticized polymeric membranes – one of the most popular sensor membrane materials nowadays. Not too many research works were devoted to this problem in the last years. Here we report on the successful development of several novel sulfate ionophores based on the synthetic modification of the commercially available sulfate ionophore I. The newly developed sensors outperform commercial analogue in terms of elelctrochemical sensitivity and selectivity. We have highlighted certain problems with numerical selectivity assessment in case when primary and interfering ions have different charges. The counterintuitive results yielded by conventional selectivity quantification methods implies the relevance of using alternative approach – visualizing sensor response curves towards primary ion in the presence of interfering ions. Novel sulfate sensors were applied for direct potentiometric measurements of sulfate content in river water samples demonstrating real applicability of the developed sensor membranes.

Mass Spectrometry Imaging for the Characterization of C═C Localization in Unsaturated Lipid Isomers at the Single-Cell Level.

Unsaturated lipids with carbon-carbon double bonds (C═C) have been implicated in the pathogenesis of various diseases. While mass spectrometry imaging (MSI) has been employed to map the distribution of lipid isomers in tissue sections, the identification of lipid C═C positional isomers at the single-cell level using MSI poses a significant challenge. In this study, we developed a novel approach utilizing ToF-SIMS in conjunction with the Paternò-Büchi (P-B) photochemical reaction to characterize the C═C localization in unsaturated lipid isomers at the single-cell level. The P-B reaction was employed to produce adduct products, which were subsequently subjected to collision-induced dissociation by the primary ion beam of ToF-SIMS to generate characteristic ion pairs indicative of the presence of C═C bonds. Utilizing this approach, lipid isomers in brain and skeletal tissues from mice, as well as different cell lines, were visualized at single-cell resolution. Furthermore, distinct variations in the composition of FA 18:1 isomers across different microregions and cell types were revealed. Our P-B ToF-SIMS approach enables the accurate identification and characterization of complex lipid structures with remarkable spatial resolution and can be helpful in understanding the physiological role of these C═C positional isomers.

Hydrogeochemical characteristics and agricultural suitability of shallow groundwater quality in a concentrated coalfield area of Huaibei Plain, China.

Groundwater is one of the chief water sources for agricultural activities in an aggregation of coal mines surrounded by agricultural areas in the Huaibei Plain. However, there have been few reports on whether mining-affected groundwater can be adopted for agricultural irrigation. We attempted to address this question through collecting 71 shallow groundwater samples from 12 coal mining locations. The Piper trilinear chart, the Gibbs diagram, the proportional coefficient of major ions, and principal component analysis were examined to characterize the source, origin, and formation process of groundwater chemical composition. The suitability for agricultural irrigation was evaluated by a final zonation map that establishes a comprehensive weighting model based on analytic hierarchy process and criteria importance though the intercriteria correlation (AHP-CRITIC). The results revealed that the groundwater was classified as marginally alkaline water with a predominant cation of HCO3- and anion of Na+. Total hardness, total dissolved solids, sulfate (SO42-), sodium (Na+), and fluoride (F-) were the primary ions that exceeded the standard. The results also indicated that the dominant hydrochemical facies were Ca-HCO3 and Na-Cl. The dissolution of carbonate, silicate, sulfate minerals, along with cation exchange, were the main natural drivers controlling the hydrogeochemical process of groundwater. The zonation map suggested that 43.17%, 18.85%, and 37.98% of the study area were high, mediate, and low suitability zones, respectively. These results from this study can support policymakers for better managing groundwater associated with a concentration of underground coal mines.

Fluorination Promotes Lithium Salt Dissolution in Borate Esters for Lithium Metal Batteries

Lithium metal batteries promise higher energy densities than current lithium-ion batteries but require novel electrolytes to extend their cycle life. To promote electrolyte stability against lithium metal and improve the reversibility of lithium deposition/stripping, several electrolyte design strategies have been pursued. For example, high concentration electrolytes (HCEs) and localized high concentration electrolytes (LHCEs) produce solvation structure rich in salt aggregates and ion pairs, which can increase lithium metal cycling Coulombic efficiency to as high as 99.5%. Recently, molecular design of fluorinated ether solvents also leads to high lithium metal Coulombic efficiency of up to 99.9% in single-solvent-single-salt ~ 1 M electrolytes. In addition, fluorinated acetals, fluorinated carbonates, and fluorinated sulfonamides are also reported to enable efficient lithium metal cycling. Among those novel electrolytes, fluorinated solvents or diluents are frequently used because fluorinated moieties are known to yield LiF as a preferable component in solid electrolyte interphase (SEI). However, fluorinated groups are believed to weaken ion solvation as most fluorinated solvents show poorer solvation ability or lower ionic conductivity compared to their nonfluorinated counterparts. The trade-off between SEI passivation and ion solvation limits further optimization of fluorinated electrolytes.In this work, we synthesize tris(2-fluoroethyl) borate (TFEB) as a new fluorinated borate ester solvent. Interestingly, moderately fluorinated TFEB shows unexpectedly high lithium salt solubility (~1 M LiFSA) while the nonfluorinated triethyl borate (TEB) and heavily fluorinated tris(2,2,2-trifluoroethyl) borate (TTFEB) can hardly dissolve lithium salt. Through density functional theory (DFT) calculations and ab-initio molecular dynamics (AIMD) simulations, we show that the partially fluorinated -CH2F group in TFEB acts as primary coordination site that promotes lithium salt dissolution. The electrochemical property of TFEB electrolyte is then compared to the methoxy polyethyleneglycol borate esters reported in literature. Owing to the fluorinated solvent structure, TFEB electrolyte passivates lithium metal with LiF-rich SEI and supports compact lithium deposition morphology, high lithium metal Coulombic efficiency, and stable cycling of lithium metal/LiFePO4 cells. This work ushers in a new electrolyte design paradigm where partially fluorinated moieties enable salt dissolution and can serve as primary ion coordination sites for next-generation electrolytes. Figure 1

Helium metastable density determination in the COST reference source by absolutely calibrated optical emission spectroscopy

Helium metastable densities in the COST Reference Microplasma Jet are estimated for a variety of He/N2 admixtures and dissipated powers by applying a collisional-radiative model to absolutely calibrated optical emission spectroscopy measurements. This is accomplished by delineating the excitation mechanisms that result in the N2(C–B) and N2+(B–X) emission bands, the latter of which is strongly coupled to the presence of helium metastables. A number of other plasma parameters are established and discussed for each operating condition including the electron energy distribution function, reduced electric field, rate constants, and electron density. With these parameters, the reaction rates for the primary ionization pathways are also calculated, emphasizing the importance of helium metastables for discharge sustainment. Good agreement with the existing literature is found for most plasma parameters and for helium metastable densities, in particular. A clear [N2]−1 relationship between the nitrogen concentration and density of helium metastables is demonstrated, as has been identified in previous studies in analogous atmospheric pressure plasma jets. This validates the efficacy of this optical technique for determining helium metastable densities and establishes it as a viable, and in many cases, more accessible alternative to other means of quantifying helium metastables in low-temperature plasmas.

Development of a Cone Homooxacalix[3]arene-Based Fluorescent Chemosensor for the Selective Detection of Biogenic Ammonium Ions in Protic Solvents.

We report here on the development of a fluorescent cone homooxacalix[3]arene-based receptor with a pyrene unit on the wide rim of the macrocycle (Ox3F) for the selective detection of primary ammonium ions, including those of biological importance. Ox3F was synthesized efficiently via an innovative strategy that enables the regio- and iteroselective wide rim functionalization of the readily available p-tBu-substituted homooxacalix[3]arene precursor. Nuclear magnetic resonance studies and in silico methods highlighted the endo-complexation of primary ammonium ions, including the protonated form of biogenic dopamine, tryptamine, serotonin, mexamine, and 3-iodothyronamine. The binding mode is similar for all guests with the ion deeply inserted into the polyaromatic cavity, enabling the NH3+ head to establish three hydrogen bonds with the ethereal oxygens of the macrocycle. Fluorescence quenching of the pyrene unit was observed following the π-π interaction between the pyrene moiety and the aromatic groups of serotonin, mexamine, and 3-iodothyronamine. No quenching was observed upon complexation of the smaller aromatic neurotransmitter dopamine as well as aliphatic amines and polyamines. This study presents a novel approach for biologically relevant ammonium ion chemosensing with ongoing efforts focused on translating these systems for aqueous environment applications.

Chemical characteristics, formation mechanisms, and geological evolution processes of high-salinity coal reservoir water in the Binchang area of the southern Ordos Basin, China

The chemical characteristics of coal reservoir water are important for studying the formation and enrichment of biogenic coalbed methane (BCM). Based on geological and sampling test data, this paper studied the geochemical characteristics and formation mechanisms of high-salinity coal reservoir water (CRW) in the Jurassic Yan'an Formation of the Binchang area in the southern Ordos Basin. The results show that the TDS contents of the CRW in the Binchang area are between 7577.38 and 15,138.61 mg/L (av. 13,268.95 mg/L), which is high-salinity brackish water. The ion types of CRW are mainly Na+, Cl− and HCO3−, and the correlations between TDS and Na+ and Cl− are close to 1. The Piper trilinear diagram indicates that the evolution direction of the CRW is deep concentrated brine, and the hydrochemical type is the NaCl type. The 127I concentrations of CRW are between 285 and 484 μg/L, which are much higher than the values of 55.88 μg/L for seawater. The results of 129I dating show that the minimum age of the CRW in the study area is between 6.7 Ma and 39.97 Ma, which is much younger than the actual geological age of the Yan'an Formation. The hydrogen and oxygen isotope results show that the CRW in the study area experiences an apparent oxygen drift, indicating that the coal reservoir of the Yan'an Formation has good sealing and a long retention time for the CRW. The hydrodynamic factors show that the hydrodynamic conditions of the coal reservoir are weak, and the primary ions in the CRW originated from the dissolution of salt rocks. The main ion differentiation indices show that high-salinity coal seam water is mainly formed by evaporation, and the ion exchange between CRW and the surrounding rock and the alternating adsorption of cations in water are very weak. Evaporation and diagenesis lead to an increase in the contents of Na+, Cl− and I+ in coalbed water, which in turn leads to an increase in the total dissolved solids contents of CRW and its evolution toward concentrated brine. The genesis and evolution of the CRW in the study area are affected by the combination of the relationships among the paleoclimate, aquifers and aquifuges, and tectonic evolution processes. The CRW in the study area has experienced five evolution stages, i.e., sedimentary water and diagenetic water, high-salinity infiltration water, primary mixed water, paleoatmospheric precipitation recharge water, and secondary mixed water. The above understanding can provide a basis for studying the formation period and accumulation mechanism of BCM and provide a hydrogeological basis for water resource utilisation and pollution prevention and the control of high-salinity water.

Soft ionization mechanisms in flexible µ-tube plasma—elucidation of He-, Ar-, Kr-, and Xe-FµTP

The soft ionization mechanism of helium-based plasma seems to be understood while it still remains challenging in argon-based plasma, although many studies have used argon plasmas as a soft ionization source with good ionization efficiencies. In this study, helium, argon, krypton, and xenon were fed into the same discharge geometry, a flexible micro-tube plasma (FµTP), to determine the ionization mechanisms. The FµTPs operated with the named noble gases obtained comparable ionization efficiencies by MS measurements. The optical emission results showed that N2+ were the dominant ions within the helium-FµTP and noble gas ions were dominant for the other plasmas. These ions support the development of excitation and eventually stop at the end of the capillary. Therefore, Penning ionization and charge transfer between plasma and ambient air/analytes in the open atmosphere have been proven not to be the primary soft ionization mechanism. Furthermore, it was found that photoionization played a minor role in soft ionization. Using helium as a diagnosis gas in front of the discharge capillary nozzle of the FµTP, where the sample is usually positioned, shows that helium can be ignited by all of these FµTPs. This demonstrates that the excitation of a diagnosis gas as well as the ionization of analytes is independent of the type of the discharge gas. An alternative mechanism that a transient potential created by the ions is responsible for the soft ionization is subsequently proposed.

Tof-SIMS spectra of historical inorganic pigments: Copper-, zinc-, arsenic-, and phosphorus-containing pigments in negative polarity

Time-of-flight secondary ion mass spectrometry (ToF-SIMS) is increasingly used to analyze cultural heritage materials because it can simultaneously detect organic and inorganic materials while mapping them on a surface. The precise identification of a pigment in a specific layer of a painting or of remaining color on a statue can inform about the technique used or the time of manufacture as well as expose possible forgeries when anachronistic ingredients are identified. Reference spectra are required to confidently identify a given pigment using ToF-SIMS. This paper focuses on eight pigments containing copper, zinc, arsenic, or phosphate, all manufactured following historical recipes. The negative polarity ToF-SIMS reference spectra using a Bi3+ primary ion species are presented here. Presented together, these spectra and corresponding tables of secondary ions provide a valuable help in differentiating these pigments because copper, zinc, arsenic, or phosphate, combined with oxygen, share many mass interferences.

Cationization agent affects the stability of secondary ions in MeV-SIMS

The work presents studies of the cationization agent effect on the ionization efficiency, and on the stability of secondary molecules, which are desorbed from the surface as a result of bombardment by MeV primary ions. Different organic molecule standards were mixed with various trifluoroacetate (TFA) salts, namely AgTFA, LiTFA, NaTFA and KTFA, with Ag, Li, Na and K being common cationization agents of secondary ions besides hydrogen. Results show modest differences in ionization efficiency, and significant variation of secondary ions’ stability when different cationization agents are attached to the molecule. For all reference samples, lithium provided the most stable secondary ions with almost none detected fragmentations after the desorption, while secondary ions with attached potassium were measured as much less stable, and the ratio between neutrals (fragments) and normal positive ions is estimated to be more than 0.2. However, even potassium – ionized molecules were recognized as more stable than protonated molecules.

Tof-SIMS spectra of historical inorganic pigments: Copper-, zinc-, arsenic-, and phosphorus-containing pigments in positive polarity

Time-of-flight secondary ion mass spectrometry (ToF-SIMS) is increasingly used to analyze cultural heritage materials because it can simultaneously detect organic and inorganic materials while mapping them on a surface. The precise identification of a pigment in a specific layer of a painting or of remaining color on a statue can inform about the technique used or the time of manufacture as well as expose possible forgeries when anachronistic ingredients are identified. Reference spectra are required to confidently identify a given pigment using ToF-SIMS. This paper focuses on eight pigments containing copper, zinc, arsenic, or phosphate, all manufactured following historical recipes. The positive polarity ToF-SIMS reference spectra using a Bi3 + primary ion species are presented here. Presented together, these spectra and corresponding tables of secondary ions provide a valuable help in differentiating these pigments, because copper, zinc, arsenic, or phosphate, combined with oxygen, share many mass interferences.

Evaluation of the pH and Antibacterial Efficacy of Mineral Trioxide Aggregate With and Without the Incorporation of Titanium Tetrafluoride.

Introduction Microorganisms play an important role in causing inflammation in the pulp and periapical regions. Even after undergoing chemo-mechanical procedures during root canal treatment, bacteria may persist within dentinal tubules, posing a risk of disease recurrence. Mineral trioxide aggregate (MTA), introduced as a dental material, has been investigated as a potential antibacterial agent since its early use. Calcium and phosphorus are the primary ions in MTA, and their antibacterial characteristics are attributed to the release of calcium hydroxide through surface hydrolysis of calcium silicate components. Previous studies have shown that MTA has limited antimicrobial properties. Several alterations have been made to enhance the biological properties of MTA, such as incorporating nanoparticles made from silver, zinc, gold, and titanium. Therefore, in this study, titanium tetrafluoride (TiF4) was added to MTA in an effort to enhance its antimicrobial properties. Aim To compare and evaluate the antibacterial efficacy of MTA after the incorporation of TiF4. Materials and methods A total of 56 samples were made by mixing MTA with different weight proportions of TiF4 (1 wt%, 2 wt%, and 3 wt%). Out of these, 28 samples were taken to test each of the following properties: antibacterial efficacy and pH. The specimens were prepared using stainless steel molds of recommended dimensions for testing the pH. The pH was evaluated using a pH meter, and the antibacterial efficacy was assessed using the direct contact test. Data regarding the antibacterial efficacy and pH of MTA with various proportions of TiF4 were investigated for normality using the Kolmogorov-Smirnov test and assessed for normal distribution. The antibacterial properties among the four groups were analyzed using one-way analysis of variance (ANOVA), followed by pairwise multiple comparisons using Tukey's Honest Significant Difference test. The level of statistical significance was determined at p ≤ 0.05. MTA, when incorporated with TiF4, showed enhanced antibacterial properties. Results On day 1, the group treated with MTA containing 3% TiF4 demonstrated the strongest antibacterial effectiveness, with a mean of 4.67 ± 0.04 colony-forming units (CFU)/mL × 10^8. However, the group treated with plain MTA had the lowest mean values, at 5.67 ± 0.25 CFU/mL × 10^8. On day 1, the MTA group with 3% TiF4 also had the highest mean pH values (11.90 ± 0.05), while the plain MTA group had the lowest mean pH values (11.64 ± 0.78). On day 7, the MTA group with 3% TiF4 had the highest pH value (12.85 ± 0.08), whereas the plain MTA group had the lowest pH value (11.92 ± 0.09). Conclusion The inclusion of TiF4 resulted in an augmentation of the antibacterial efficacy of MTA against Enterococcus faecalis (E. faecalis). Hence, the integration of TiF4 into MTA can be considered a promising development against E. faecalis during endodontic procedures.