Search Results (120)

There are many types of probes available on the market for measuring ambient dose equivalent rates (ADERs), which makes intercomparison exercises essential to ensure data comparability and reliability. This study evaluated the performance of four widely used and similarly priced probes—the Reuter-Stokes ionization chamber, the RX04L from BITT, the MIRA from ENVINET, and the LB9360 from Berthold. The Reuter-Stokes ionization chamber was also taken as reference. Measurements were continuously conducted in Bilbao, northern Spain, during the period 2017–2021 under background conditions as well as during episodes of heavy rainfall and extreme temperatures. Results show that the BITT proportional counter exhibited the highest consistency with the Reuter-Stokes chamber under all meteorological conditions, and excellent stability even during extreme conditions. The Berthold probe displayed similar trends, but systematically overestimated dose rates, while the Geiger–Müller-based detector showed acceptable agreement under rainfall, but clear instability during temperature extremes. These findings highlight the importance of probe selection in environmental radioactivity networks as well as the use of reliable instruments for integration into modernized radiological surveillance systems. Full article

Chlorpyrifos CPF (O,O-diethyl O-(3,5,6-trichloro-2-pyridyl) phosphorothioate), known also as Chlorpyrifos-ethyl, is one of the most utilized organophosphorus pesticides worldwide. Additionally, CPF could be used as a chemical warfare agent surrogate. Although its acute toxicity is not high, it is responsible for both a large number of intoxications and chronic, delayed neurological effects. In this work, it is reported for the first time the qualitative and quantitative response produced by CPF vapors, using a pocket-held Time-of-Flight Ion Mobility Spectrometer (ToF IMS) with a non-radioactive ionization source and ammonia doping, model LCD-3.2E (Smiths Detection Ltd.), operated near ambient temperature (below 30 °C). Spectra of CPF in positive ion mode included two distinct product ion peaks; thus, identification of CPF vapors by IMS relies on these peaks—the monomer M·NH₄⁺ with reduced ion mobility K₀ = ca. 1.76 cm² V⁻¹ s⁻¹ and the dimer M₂·NH₄⁺ with K₀ = ca. 1.47 cm² V⁻¹ s⁻¹ (where M may be assignable to CPF molecule)—and positive reactant ions (Pos RIP) have K₀ = ca. 2.25 cm² V⁻¹ s⁻¹. Excellent sensitivity, with a limit of detection LOD of 0.72 ppb_v (10.5 μg m⁻³) and a limit of quantification LOQ of 2.41 ppb_v (35.1 μg m⁻³), has been noticed; linear response was up to 100 ppb_v, while saturation occurs over ca. 1000 ppb_v (14.6 mg m⁻³). Our results demonstrate that this method provides a robust tool for both off-site and on-site detecting and quantifying CPF vapors at trace levels, which has strong implications for either industrial hygiene or forensic investigations concerning the pesticide Chlorpyrifos, as well as for monitoring of environmental contamination by organophosphorus pesticides. Full article

Investigating atmospheric volatile organic compounds (VOCs) is critical for understanding their sources, chemical reactivity, and impacts on air quality, climate, and human health, especially in remote regions like the Tibetan Plateau where baseline data remains scarce. In this study, ambient VOCs species were simultaneously measured at four remote background sites on the Tibetan Plateau (Nyingchi, Namtso, Ngari, and Mount Everest) from 2012 to 2014 to investigate their concentration, composition, sources, and chemical reactivity. Weekly integrated samples were collected and analyzed using a Gas Chromatograph-Mass Spectrometer/Flame Ionization Detector (GC-MS/FID) system. The total VOC mixing ratios exhibited site-dependent variability, with the highest levels observed in Nyingchi, followed by Mount Everest, Ngari and Namtso. The VOC composition in those remote sites was dominated by alkanes (25.7–48.5%) and aromatics (11.4–34.7%), followed by halocarbons (19.1–28.1%) and alkenes (11.5–18.5%). A distinct seasonal trend was observed, with higher VOC concentrations in summer and lower levels in spring and autumn. Source analysis based on correlations between specific VOC species suggests that combustion emissions (e.g., biomass burning or residential heating) were a major contributor during winter and spring, while traffic-related emissions influenced summer VOC levels. In addition, long-range transport of pollutants from South Asia also significantly impacted VOC concentrations across the plateau. Furthermore, reactivity assessments indicated that alkenes were the dominant contributors to OH radical loss rates, whereas aromatics were the largest drivers of ozone formation potential (OFP). These findings highlight the complex interplay of local emissions and regional transport in shaping VOC chemistry in this high-altitude background environment, with implications for atmospheric oxidation capacity and secondary pollutant formation. Full article

This paper introduces a novel Lateral Extraction Enhanced Desorption Electrospray Ionization (LEE-DESI) source. This source is specifically designed to tackle the crucial issue of electric field interference in dual-channel ambient ionization mass spectrometry (AIMS). By incorporating dual-channel spraying-based desorption and extraction into a 3D-printed chamber with optimized spatial parameters, the system effectively reduces cross-channel interference while boosting ionization efficiency. The desorption spray is responsible for desorbing analytes from untreated samples, and the extraction spray further ionizes more neutral droplets through charge transfer, which substantially enhances sensitivity. Compared with traditional DESI, the LEE-DESI source demonstrates improved detection limits, reproducibility, and operational simplicity, as validated using Rhodamine B, L-arginine, and Angiotensin I, as well as drug standards including methadone, ketamine, and fentanyl. This highlights its potential for high-throughput analysis of complex matrices in proteomics, metabolomics, and biomedical applications. Full article

Different polyurethanes (PURs) and silicone for potential use in particle accelerators and detectors have been characterized in the uncured state, after curing, and after exposure to ionizing irradiation in ambient air and in liquid helium. The viscosity evolution during processing was measured with a rheometer. Dynamic mechanical analysis (DMA) and Shore A hardness measurements were applied to detect irradiation-induced crosslinking and chain scission effects. Uniaxial tensile and flexural tests under ambient and cryogenic conditions have been performed to assess changes in mechanical strength, elongation at break, and elastic properties. The initial viscosity of 550 cP at 25 °C of the uncured PUR RE700-4 polyol and RE106 isocyanate system for protective encapsulation is sufficiently low for impregnation of small magnet coils, but the pot life of about 30 min is too short for impregnation of large magnet coils. The cured RE700-4 system has outstanding mechanical properties at 77 K (flexural strength, impact strength, and fracture toughness). When RE700-4 is exposed to ionizing radiation, chain scission and cross-linking occur at a similar rate. In the other casting systems, irradiation-induced changes are cross-linking dominated, as manifested by an increase of the rubbery shear modulus (G’_rubbery), the ambient temperature Young’s modulus (E_RT), and the Shore A hardness. Cross-linking rates are strongly reduced when irradiation occurs in liquid helium. The irradiation effect on mechanical properties can be strongly dependent on the testing temperature. The RT mechanical strength and strain at fracture of the cross-linking silicone is drastically decreased after 1.6 MGy, whereas its 77 K strain at fracture has almost doubled. In addition, 77 K elastic moduli are similar for all pure resins and only slightly affected by irradiation. Full article

Irradiation combined with Modified Atmosphere (MA) Packaging (MAP) is increasingly applied to disinfest fresh harvested produce while maintaining quality. However, anoxia and hypoxic conditions created by MA can reduce the effectiveness of ionizing radiation by inducing radioprotective effects in insects. This study investigated the relationship between oxygen levels and radiation efficacy in late third-instar larvae of Zeugodacus cucurbitae. Larvae were sealed in MAP bags filled with various low-oxygen atmospheres (0% to 5%, nitrogen balance) or ambient air (21%) and irradiated with X-rays at doses from 16 to 88 Gy. Mortality was assessed based on adult emergence. Results showed that mortality significantly decreased as oxygen level increased from 0% to 3%, and statistic data-analysis including probit analysis showed a critical oxygen threshold at 4% O₂. At oxygen levels below this threshold, significantly higher radiation doses were required to achieve 99.9968% mortality at a 95% confidence level (probit-9 level). The additional dose needed under 0% O₂ was estimated at 13–18 Gy compared to ambient air. These findings further demonstrate that phytosanitary irradiation under MA conditions can effectively control tephritid insects while preserving product quality. Identifying 4% O₂ as the radioprotective threshold may have implications for understanding dose–response mechanisms under MA conditions. Full article

Narcotics trafficking is a fundamental part of organized crime, posing significant and evolving challenges for forensic investigations. Addressing these challenges requires rapid, precise, and scientifically validated analytical methods for reliable identification of illicit substances. Over the past five years, forensic drug testing has advanced considerably, improving detection of traditional drugs—such as tetrahydrocannabinol, cocaine, heroin, amphetamine-type stimulants, and lysergic acid diethylamide—as well as emerging new psychoactive substances (NPS), including synthetic cannabinoids (e.g., 5F-MDMB-PICA), cathinones (e.g., α-PVP), potent opioids (e.g., carfentanil), designer psychedelics (e.g., 25I-NBOMe), benzodiazepines (e.g., flualprazolam), and dissociatives (e.g., 3-HO-PCP). Current technologies include colorimetric assays, ambient ionization mass spectrometry, and chromatographic methods coupled with various detectors, all enhancing accuracy and precision. Vibrational spectroscopy techniques, like Raman and Fourier transform infrared spectroscopy, have become essential for non-destructive identification. Additionally, new sensors with disposable electrodes and miniaturized transducers allow ultrasensitive on-site detection of drugs and metabolites. Advanced chemometric algorithms extract maximum information from complex data, enabling faster and more reliable identifications. An important emerging trend is the adoption of green analytical methods—including direct analysis, solvent-free extraction, miniaturized instruments, and eco-friendly chromatographic processes—that reduce environmental impact without sacrificing performance. This review provides a comprehensive overview of innovations over the last five years in forensic drug analysis based on the ScienceDirect database and highlights technological trends shaping the future of forensic toxicology. Full article

Hypocalcemia is common in dairy cows within the first 72 h post-calving, and can be either clinical or subclinical. Early detection is critical, but traditional laboratory tests are time-consuming and cow-side tests remain costly. A classic symptom of hypocalcemia is reduced ear skin temperature, which has been explored as a diagnostic tool in a previous study, but was not recommended at the end. Additionally, ambient temperature was found to strongly influence ear skin temperature, complicating diagnosis. The present study investigates infrared thermography of the ear as a potential non-invasive method for helping in the detection of hypocalcemia in Holstein cows. In order to differ from the previous study, with the goal of improving diagnosis accuracy, this research analyzed the entire ear temperature using infrared imaging software. Ambient temperature was factored in by categorizing samples into two groups based on air temperature: colder (−1.6 to 14.6 °C) and hotter (15.3 to 31.2 °C). Forty-two cows were monitored during the perinatal period, with blood samples and thermographic images taken twice a day until 48 h after calving. This study found that the median surface temperature of the ear correlated strongly with environmental temperature (r = 0.806, p < 0.001) and weakly with blood ionized calcium levels (r = 0.310, p < 0.01). In colder air temperatures, ear surface temperature was significantly different between healthy and hypocalcemic cows (p = 0.014). Logistic regression models were used to assess ionized calcium status based on different combinations of ear surface temperature, its difference from air temperature, and days in milk. In hotter air temperatures, only ear surface temperature, with no other covariates, was able to generate a valid model (p = 0.029). In colder air temperatures, multiple combinations of those variables generated valid models (p < 0.05), with the difference between ear and air temperature, together with days in milk, performing the best. Thus, this study concluded that ear surface temperature obtained through infrared thermography, while not promising for warmer environments, does show application potential for helping in the detection of hypocalcemia in colder environments. Full article

Benzene, toluene, ethylbenzene, and xylene (BTEX) are widespread volatile organic compounds commonly present in fuels and various industrial materials. Their release into the atmosphere significantly contributes to air pollution, prompting strict regulatory concentration limits in ambient air. In this work, we introduce Multiphoton Electron Extraction Spectroscopy (MEES) as an innovative technique for the sensitive, selective, and online detection and quantitation of BTEX compounds under ambient conditions. MEES employs tunable UV laser pulses to induce the resonant ionization of target molecules under a high electrical field, with subsequent measurement of the generated photocurrent. We now demonstrate the method’s ability to detect BTEX in ambient air, at part-per-trillion (ppt) concentration range, providing distinct spectral signatures for each compound, including individual xylene isomers. The technique represents a significant advancement in BTEX monitoring, with potential applications in environmental sensing and industrial air quality control. Full article

We present a simple and cost-effective method for generating a dielectric barrier discharge (DBD) plasma using a commercially available ozone generator power supply. By coupling the plasma source to the extended ion transfer tube of an ambient mass spectrometer, we achieved stable plasma discharge, enabling the post-ionization of nonpolar compounds during the electrospray ionization process. Using this approach, we successfully detected polycyclic aromatic hydrocarbons (PAHs), halogenated PAHs (HPAHs), and other nonpolar pollutants in liquid mixtures, with detection limits on the order of 10 ng/mL. In fish exposed to HPAHs, both polar metabolites and lipids, as well as the nonpolar pollutant 1-chloronaphthalene, were simultaneously detected. Notably, 1-chloronaphthalene accumulated at the highest concentration in gill tissue. This straightforward plasma-assisted technique offers a reliable strategy for expanding the detection capabilities of electrospray mass spectrometry to include nonpolar molecules. Full article

Background: In response to the growing demand for the real-time, in-field characterization of odorous anthropogenic emissions, this study develops and uses a MEMS-based micropacked thermal desorption Gas Chromatography system coupled with a PhotoIonization Detector (GC/PID) for Hot Mix Asphalt (HMA) plant emissions. Methods: The innovative portable device, Pyxis GC, enables the high-sensitivity profiling of Volatile Organic Compounds (VOCs), particularly aldehydes and ketones, with sub-ppb detection limits using ambient air as the carrier gas. A comprehensive experimental design optimized the preconcentration parameters, resulting in an efficient, green analytical method evaluated via the Green Analytical Procedure Index (GAPI). Sorbent comparison showed quinoxaline-bridged cavitands outperform the conventional materials. Results and conclusions: The method was successfully deployed on site for source-specific sampling at an HMA plant, generating robust emission fingerprints. To assess environmental impact, a Generalized Additive Model (GAM) was developed, incorporating the process temperature and Sum of Odour Activity Values (SOAV) to predict odour concentrations. The model revealed a significant non-linear influence of temperature on emissions and validated its predictive capability despite the limited sample size. This integrated analytical–statistical approach demonstrates the utility of MEMS technology for real-time air quality assessment and odour dispersion modelling, offering a powerful tool for environmental monitoring and regulatory compliance. Full article

Eulerian observations of chemical species at fixed positions in a flow field are known to violate conservation laws, while observations tracking moving air parcels are practically unfeasible. Eulerian observations often cause positive correlations between the reactants and products in the atmosphere, which are frequently misinterpreted as evidence of the related chemical conversion. This dilemma has motivated innovative trials. The perturbation technique, widely used in mathematical and physical studies, offers a potential solution. Combining Eulerian observations with perturbation techniques may compensate for this weakness, making this approach particularly valuable for studying the gas–aerosol partitioning of semi-volatile particulate species in ambient air. As an example, we examined this combination through an adiabatic-expansion-induced perturbation study of the gas–aerosol partitioning of dimethylamine (DMA) and trimethylamine (TMA) in ambient air. Eulerian observations of chemical species in size-segregated atmospheric particles ranging from 10 μm to 0.056 μm, coupled with downstream adiabatic-expansion-induced perturbation observations, were performed in coastal and marine atmospheres using a commercial sampler (Nano-MOUDI-II, MSP, Shoreview, MN, USA), followed by an offline chemical analysis. The results revealed that particulate DMA generally tended to evaporate in ambient air during the observational periods, while enhanced adiabatic-expansion-induced perturbations occasionally led to the co-formation of DMAHNO₃ and NH₄NO₃. However, gaseous TMA apparently underwent gas–particle condensation to reach equilibrium in ambient air, with adiabatic-expansion-induced perturbation resulting in the formation of non-ionized TMA particulates. The thermodynamic analysis further supported that the observed particulate TMA was primarily determined by the equilibrium of gaseous TMA with non-ionized particulate TMA rather than ionic TMAH⁺. Full article

Serial crystallography is a rapidly advancing experimental technology that has seen significant development in recent years. This technique enables the continuous delivery of a series of protein crystal samples to the X-ray beam, allowing for the collection of diffraction data from a large number of crystals at ambient temperature. Despite its advancements, serial crystallography still possesses considerable potential for further development within synchrotron radiation platforms. Currently, several challenges hinder the progress of this technology, including the preparation of numerous microcrystal samples, methods for sample delivery, data acquisition efficiency, and data processing techniques. The device introduced in this paper is designed to facilitate serial crystallographic experiments at the synchrotron radiation station, employing electrospinning in the vacuum cavity to reduce the average flux, mitigate the effects of air ionization on the Taylor cone, and enhance the stability of Taylor cone during the data acquisition process. The diffraction pattern of lysozyme crystals was successfully acquired with this device at the beamlines of the Shanghai Synchrotron Radiation Facility (SSRF). Full article

Anastomotic leaks remain a significant challenge in intestinal surgery, often leading to severe complications. This study investigated a novel approach to enhance anastomotic healing and reduce the risk of leaks by combining traditional suturing and stapling techniques with non-thermal atmospheric pressure plasma (NTAPP) application. NTAPP, a cold atmospheric plasma generated through the ionization of ambient air, has been shown to possess antimicrobial, hemostatic, and wound-healing properties. NTAPP promotes sterilization, coagulation, and tissue regeneration by generating reactive oxygen and nitrogen species, potentially strengthening anastomotic union. This pilot study evaluated the efficacy of NTAPP in three patients undergoing intestinal anastomosis. Following the standard surgical procedure, NTAPP was applied directly to the anastomotic site. Postoperative outcomes were monitored for six months, including anastomotic leaks and healing rates. Preliminary results demonstrated promising outcomes. All three patients exhibited successful sealing of the anastomosis, with no evidence of leakage during the follow-up period, providing reassurance and confidence in the potential of sutures, staples, and NTAPP. These findings suggest that NTAPP can significantly improve the safety and efficacy of intestinal surgeries by reducing the incidence of anastomotic leaks. While further research with a larger sample is necessary to confirm these initial findings, the results of this study provide a strong foundation for exploring the potential of NTAPP as a valuable adjunct to conventional surgical techniques for preventing anastomotic leaks. This innovative approach could reduce postoperative complications, improve patient outcomes, and enhance the overall quality of care in intestinal surgery. Full article

Using first-principles density functional theory (DFT) calculations and ab initio molecular dynamics (AIMD) simulations, we performed this study on the phase stability, the intrinsic redox stability, and the Li⁺ conductivity of Li₁₀Ge_xMo_1−xP₂S₁₂ (x = 0~1) superionic conductors. Molybdenum (Mo) is expected to replace expensive germanium (Ge) to lower tmaterial costs, reduce sensitivity to ambient water and oxygen, and achieve acceptable Li⁺ conductivity. The ab initio first principle molecular dynamics simulations show that room-temperature Li⁺ conductivity is 1.12 mS·cm⁻¹ for the Li₁₀Ge_0.75Mo_0.25P₂S₁₂ compound, which is comparable to the theoretical value of 6.81 mS·cm⁻¹ and the experimental measured one of 12 mS·cm⁻¹ of the Li₁₀GeP₂S₁₂ (LGPS) structure. For Li₁₀Ge_xMo_1−xP₂S₁₂ (x = 0, 0.25, 0.5 and 1) compounds, the density of states and the projection fractional wave state density were calculated. It was found that when Ge atoms were partially replaced by Mo atoms, the band gap remained unchanged at 2.5 eV, but deep level defects appeared in Mo-substituted compounds. Fortunately, this deep level defect is difficult to ionize at room temperature, so it has no effect on the electronic conductivity of Mo substitute compounds, making Mo substitution a suitable solution for electrolyte materials. The projection fractional wave state density calculation shows that the covalent bond between Mo and S is stronger than that between Ge and S, which reduces the sensitivity of Mo-substituted compounds to water and oxygen contents in the air. In addition, the partial state density coincidence curve between Li and S elements disappears in the 25% Mo-substituted compound with energies of 4–5 eV, indicating that the Li₂S by-product is decreased. Full article