Kinetic Parameters Research Articles

Two-Stage Global Biomass Pyrolysis Model for Combustion Applications: Predicting Product Composition with a Focus on Kinetics, Energy, and Mass Balances Consistency

This work presents a comprehensive model for lignocellulosic biomass pyrolysis, addressing kinetics, energy balances, and gas product composition with the aim of its application in wood combustion. The model consists of a two-stage global mechanism in which biomass initially reacts into tar, char, and light gases (non-condensable gases), which is followed by tar reacting into light gases and char. Experimental data from the literature are employed for determining Arrhenius kinetic parameters and key energy parameters, like tar and char heating values and the specific enthalpy of primary and secondary reactions. A methodology is introduced to derive correlations, allowing the model’s application to diverse biomass types. This work introduces several novel approaches. Firstly, a pyrolysis model that determines the composition of light gases by solving mass, species, and energy balances is developed, limiting the use of correlations from the literature only for tar and char elemental composition. The mass rate of light gases, tar, and char being produced is also determined. Secondly, kinetic parameters for primary and secondary reactions are determined following a Shafizadeh and Chin scheme but with a modified Arrhenius form dependent on Tn, significantly enhancing the accuracy of product composition prediction. Additionally, correlations for the enthalpies of reactions, both primary and secondary, are determined as a function of pyrolysis temperature. Primary reactions exhibit an overall endothermic behavior, while secondary reactions exhibit an overall exothermic behavior. Finally, the model is validated using cases reported in the literature, and results for light gases composition are presented.

Single time-point analysis of product and substrate inhibition.

When enzyme inhibition by either the product or excess substrate occurs, it is possible to determine the characteristic kinetic parameters based on [P]/t measurements, even when a large proportion of the substrate is converted. The advantages of various approaches are discussed. Most of them allow a good estimation of the V and Km values. Conversely, the determination of Kp (product inhibition) and Ki (inhibition by excess substrate) can be more challenging. In the first case, determination of the type of inhibition requires more complex experiments that are beyond the scope of the present contribution. In the second, the inhibition constant Ki can only be roughly estimated. In an experimental approach, we compared the results obtained either with initial rate measurements or with 50 to 60% conversion of the substrate. Similar values of V and Km were obtained. Measurements involving the conversion of a large proportion of substrate are particularly advantageous when the assay method is difficult or time-consuming, or when obtaining the substrate presents experimental difficulties or involves substantial costs.

Hydrothermal precipitation of copper from leaching solutions of metallurgical dusts

In this work, we aim to establish the main regularities of hydrothermal precipitation of copper from the previously unstudied sulfuric-nitric acid and sulfate solutions of atmospheric and autoclave processing of metallurgical dusts. Pyrite was used as a sulfidizer. The elemental composition of the products was determined by X-ray fluorescence, inductively coupled plasma atomic emission spectrometry, and atomic absorption analysis. It was found that copper precipitation by the proposed technology enables its recovery at a level of more than 95%. For sulfate solutions with a high arsenic concentration, a two-stage scheme of oxidation-hydrothermal treatment with the following parameters was proposed: temperature 180°С, duration 2 h, oxygen consumption 0.026 dm3/g pyrite (for the 1st stage), and 200°С and 2 h (for the 2nd stage). Extraction in the cake amounted to 95.4% of copper (in the form of Cu2S) and 91.4% of arsenic (in the form of FeAsO4), which allowed further separation of these metals by flotation. An autoclave treatment of a Cu–Zn–Fe–As–NO3 solution in the presence of pyrite at 180–220°С produced the activation energy values (kJ/mol) corresponding to the kinetic regime calculated by the two methods: 64.6 by the conventional method and 60.5 by the shrinking core model. The kinetic parameters of CuSO4–H2SO4–FeS2–H2O and CuNO3–H2SO4–FeS2–H2O systems were also determined. Flotation enrichment of copper autoclave precipitation cake was shown to result in a high degree of Cu and As separation, with the recovery amounting to Cu ˃ 95% and As ˂ 5%. Precious metals contained in pyrite are transferred to a flotation concentrate by 92.7% (Au) and 96.5% (Ag). The composition of the resulting flotation concentrate comprised (%): 12 Cu; 37 Fe; 38 S; 13 other elements. It is shown that, in order to obtain a product with the required content of copper, flotation concentrate should be separated into pyrite and copper concentrates followed by an additional flotation of primary copper concentrate in an alkaline medium in the presence of lime. Hence, our study has established the main regularities of hydrothermal precipitation of copper from the sulfuric-nitric acid and sulfate solutions of atmospheric and autoclave processing of metallurgical dusts.

Dark Photon Limits from Patchy Dark Screening of the Cosmic Microwave Background.

Dark photons that kinetically mix with the Standard Model photon give rise to new spectral anisotropies (patchy dark screening) in the cosmic microwave background (CMB) due to conversion of photons to dark photons within large-scale structure. We utilize predictions for this patchy dark screening signal to provide the tightest constraints to date on the dark photon kinetic mixing parameter [ϵ≲4.5×10^{-8} (95% confidence level)] over the mass range 10^{-13} eV≲m_{A^{'}}≲10^{-11} eV, almost an order of magnitude stronger than previous limits, by applying state-of-the-art component separation techniques to the cross-correlation of Planck CMB and unWISE galaxy survey data.

Methodology for Studying Interactions of Vitamin A Membrane Receptors and Opsin Protein with their Ligands in Generating the Retinylidene Protein.

Distribution of dietary vitamin A/all-trans retinol (ROL) throughout the body is critical for maintaining retinoid function in peripheral tissues and generating the retinylidene protein for visual function. RBP4-ROL is the complex of ROL with retinol-binding protein 4 (RBP4), which is present in the blood. Two membrane receptors, Retinol Binding Protein 4 Receptor 2 (RBPR2) in the liver and STimulated by Retinoic Acid 6 Retinol (STRA6) in the eye, bind circulatory RBP4 and this mechanism is critical for internalizing ROL into cells. Establishing methods to investigate receptor-ligand kinetics is essential in understanding the physiological function of vitamin A receptors for retinoid homeostasis. Using Surface Plasmon Resonance (SPR) assays, we can analyze the binding affinities and kinetic parameters of vitamin A membrane receptors with its physiological ligand RBP4. These methodologies can reveal new structural and biochemical information of RBP4-binding motifs in RBPR2 and STRA6, which are critical for understanding pathological states of vitamin A deficiency. In the eye, internalized ROL is metabolized to 11-cis retinal, the visual chromophore that binds to opsin in photoreceptors to form the retinylidene protein, rhodopsin. The absorbance of light causes the cis-to-trans isomerization of 11-cis retinal, inducing conformational changes in rhodopsin and the subsequent activation of the phototransduction cascade. Decreased concentrations of serum and ocular ROL can impact retinylidene protein formation, which in turn can cause rhodopsin mislocalization, apoprotein opsin accumulation, night blindness, and photoreceptor outer segment degeneration, leading to Retinitis Pigmentosa or Leber Congenital Amaurosis. Therefore, spectrophotometric methodologies to quantify the G protein-coupled receptor opsin-11-cis retinal complex in the retina are critical for understanding mechanisms of retinal cell degeneration in the above-mentioned pathological states. With these comprehensive methodologies, investigators will be able to better assess dietary vitamin A supply in maintaining systemic and ocular retinoid homeostasis, which is critical for generating and maintaining retinylidene protein concentrations in photoreceptors, which is critical for sustaining visual function in humans.

Temperature-Dependent Oxidation Behavior of Silicon Carbide Surface: Reactive Molecular Dynamics Simulations.

The high-temperature oxidation mechanism of silicon carbide (SiC) is crucial for designing thermal protection systems in aircraft. This study explored the oxidative chemical reaction processes and mechanism on SiC surface and interfaces within the temperature range of 300-2300 K by using reactive molecular dynamics simulation. The oxygen impact on the silica (SiOx) growth of the SiC surface was analyzed, which shows a progressive increase of silica thickness. The simulation results indicated that the oxidation process of SiC was a typical passive oxidation mechanism. With the environmental temperature rising and oxygen impact, the increase of oxidation thickness on the SiC surface undergoes three oxidizing reaction processes: little chemical adsorption of oxygen molecules on the initial surface, rapid oxidation of silicon and carbon, and dramatic oxidation of the interface between the oxidation layer and SiC. Additionally, this work studied the mechanism of oxidation thickness growth and chemical diffusion of oxygen. The oxidation rate is weakened according to the oxygen atom diffusion barrier effect of silica repulsion. Moreover, the kinetic parameters were statistically calculated by fitting the growth of Si-O bonds and their reaction rate constants. Subsequently, the activation energy and pre-exponential factors were derived by using the Arrhenius equation to model the chemical reaction kinetics of the thermal oxidation process. The chemical reaction behaviors of the two stages could be concluded as follows: (i) in stage I, the initial oxidation is reaction rate limiting; (ii) in stage II, SiC oxidation is limited by both the oxidation reaction rate and the oxygen diffusion coefficient of the oxidation layer. The activation energy of stage II increased compared with stage I due to the oxygen atoms diffusion barrier between the oxidation layers. This study on the oxidation and ablation mechanism of the SiC surface at the atomic scale would provide insight into understanding thermal oxidation behavior and the design of ceramic materials.

2-(4-fluorobenzyl)Chromeno[2,3-c]Pyrozol-3(2H)-One as Copper Corrosion Inhibitor in HNO3: Gravimetric and Quantum Chemical Investigation Methods

The use of organic compounds as corrosion inhibitors has become a principal means of protecting metal equipment in industrial applications. This work therefore set out to evaluate the inhibiting properties of 2-(4-fluorobenzyl)chromeno[2,3-c] pyrozol-3(2H)-one for copper corrosion in 1M nitric acid solution. These properties were investigated using gravimetric method and quantum chemical calculations. Inhibition efficiency increased with temperature, inhibitor concentration and immersion time. Adsorption of this molecule on copper surface occurs according to Langmuir isotherm, while the thermodynamic parameters of absorption and kinetics prove that adsorption is spontaneous and dominated by chemisorption. Quantum chemical parameters derived from density functional theory (DFT) revealed that there is a strong interaction based on electronic exchange between the inhibitor and copper. Global and local reactivity parameters such as highest occupied molecular orbital energy, lowest unoccupied molecular orbital energy, energy gap, Fukui functions and dual descriptor were used to understand the molecule-metal interface and to design more appropriate organic corrosion inhibitors. Theoretical results proved to be consistent with the experimental data obtained.

Association Between Zinc Ion Concentrations in Seminal Plasma and Sperm Quality: A Chinese Cross-Sectional Study.

This study investigates the impacts of zinc ion concentration in in seminal plasma and the total amount of Zn2+ per ejaculation on sperm quality evaluation parameters. In addition, we assessed the reliability of using zinc content in seminal plasma to evaluate sperm quality. We analyzed semen from 964 men and found that men over 40years old had significantly lower concentrations of Zn2+ in ejaculated semen compared to other age groups (p < 0.05), with no significant difference in Zn2+ concentrations among other age groups (p > 0.05). The total amount of Zn2+ in one ejaculation did not show a statistical difference between the normal semen and the abnormal semen groups (p > 0.05). Statistical differences were observed in sperm kinetic parameters and DNA fragmentation index between the normal Zn2+ total amount group and the abnormal group (p < 0.05). However, there was no statistical difference in morphological parameters (p > 0.05). Spearman correlation analysis showed a negative correlation between Zn2+ concentrations in seminal plasma, age, and sperm fructose and a positive correlation between semen volume, abstinence time, sperm concentration, neutral α-glycosidase, and citric acid content (p < 0.05). The receiver operating characteristic curve analysis demonstrated that Zn2+ concentrations had poor accuracy and specificity in assessing sperm quality (p > 0.05). Although there is a partial correlation between Zn2+ concentrations in seminal plasma and certain semen quality parameters, relying solely on Zn2+ concentrations to evaluate sperm quality lacks accuracy and specificity.

Mechanism and process study of spent lithium iron phosphate batteries by medium-temperature oxidation roasting strategy

In this study, we determined the oxidation roasting characteristics of spent LiFePO4 battery electrode materials and applied the iso-conversion rate method and integral master plot method to analyze the kinetic parameters. The ratio of Fe (II) to Fe (III) was regulated under various oxidation conditions. The results showed that 95.50 % of LiFePO4 was oxidized to Li3Fe2(PO4)3 and Fe2O3 under the most cost-effective roasting conditions (500°C, 1000 mL/min, 30 min, air atmosphere) and only approximately 18 % graphite was involved in the reaction. More than 99 % of the lithium was leached under these roasting conditions, with minimal impurities. Medium-temperature selective oxidation roasting effectively avoided the high-temperature sintering phenomenon that affects the crystal structure of the product. Instead, a fine, uniform oxidized phase was formed, and the polyvinylidene fluoride impurity that typically persists throughout the recycling process was avoided. This study provides a sufficient theoretical basis and experimental prerequisites for selective, time-efficient, and economical lithium leaching or reductive regeneration of the cathode materials.

A Machine Learning Model for Predicting the Propagation Rate Coefficient in Free-Radical Polymerization.

The propagation rate coefficient (kp) is one of the most crucial kinetic parameters in free-radical polymerization (FRP) as it directly governs the rate of polymerization and the resulting molecular weight distribution. The kp in FRP can typically be obtained through experimental measurements or quantum chemical calculations, both of which can be time consuming and resource intensive. Herein, we developed a machine learning model based solely on the structural features of monomers involved in FRP, utilizing molecular embedding and a Lasso regression algorithm to predict kp more efficiently and accurately. The result shows that the model achieves a mean absolute percentage error (MAPE) of only 5.49% in the predictions for four new monomers, which indicates that the model exhibits strong generalization capabilities and provides reliable and robust predictions. In addition, this model can accurately predict the influence of the ester side chain length of (meth)acrylates on kp, aligning well with established scientific knowledge. This approach offers a straightforward and practical model for other researchers to rapidly obtain accurate kp values by employing monomer structural information. The model is sufficiently general to apply to a wide range of (meth)acrylate and butadiene FRP monomers, thereby supporting kinetic modeling of polymerization reactions.

Accurate measurements of delayed neutron data for reactor applications: methodology and application to 235U(nth,f)

Large inconsistencies still exist in nuclear data libraries regarding the kinetic parameters of delayed neutron (DN) precursors. As an example, there is a 17% gap between ENDF-B/VIII.0 and JEFF-3.3 on the average lifetime T1/2 of DN precursors from thermal fission of 235U. This parameter is of major importance for reactivity predictions of nuclear reactors in nominal or accidental configurations. In this context, CEA is actively participating to the ALDEN project (Average number and Lifetime of DElayed Neutrons) which aims at providing the nuclear data community with new data sets of DN from thermal and fast neutron induced fission of various actinides. A dedicated experimental setup was designed and optimized for that purpose and is presented in this paper. It consists of a “long counter” detector containing 16 proportional counters filled with 3He, embedded in a high density polyethylene matrix. The detector surrounds a fissile target prepared in the form of a miniature fission chamber, containing a few hundreds of micro-grams of fissile material. This set-up is connected to fast and efficient neutron shutters that can produce step-irradiations of variable durations. The equations driving the DN counting following step-irradiations of the fissile target are established and discussed in the perspective of DN yield or group parameter measurement. A comprehensive analysis of the different steps of data reduction is detailed: dead time characterization, Region of Interest (ROI) determination, absolute and relative efficiency calibration, fission rate estimation, irradiation time and background determination, DN decay curve production and physical parameter fitting. Following a prototype experiment performed in 2018 at the PF1b cold neutron beam line of Institute Laue Langevin (ILL, Grenoble, France), we discuss here the analysis of two campaigns occurring in 2019 and 2021 in which significant improvements were achieved in terms of background minimization, counting statistics and fission rate determination. The achievements of this work are the measurement of the delayed neutron emission per fission for the thermal neutron induced fission of 235U, estimated at (1.625 ± 0.010) % and the group parameters leading to an estimated lifetime of T1/2\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${T}_{1/2}$$\\end{document} = (8.87 ± 0.10) s. Those results are consistent with the values recommended by the IAEA/CRP work and they come with reduced uncertainties compared with previously published results.

Kinetic research of red mud waste oxidative pyrolysis and comparison under different atmospheres

Red mud, as a solid waste with high alkalinity, had a detrimental impact on the environment and required urgent attention. Currently, the mass processing and consumption of red mud were typically conducted under thermal conditions, so it was essential to gain a comprehensive understanding of the oxidative pyrolysis process. The thermogravimetric experiments were conducted at multiple heating rates in air and exhibited three obvious stages. The activation energy and reaction mechanism of three oxidative pyrolysis stages were explored using model-free and model-fitting methods, revealing the activation energies of 162.2, 265.8, 214.1 kJ/mol and the most suitable reaction mechanisms of g(α)=[-ln(1-α)]³, g(α)=1-(1-α)1/⁴, g(α)=[-ln(1-α)]1/2 for each stage, respectively. Furthermore, the estimated kinetic parameters and reaction mechanisms were applied to extra heating rate to verify the accuracy. More important, the effect of air on the pyrolysis process of red mud was examined by comparing the results with those obtained from pure nitrogen pyrolysis. The obtained oxidative pyrolysis characteristics of red mud could provide valuable insights of its co-pyrolysis or combustion for resources recycling.

Enhanced monochromatic photon emission from millicharged co-interacting dark matter

We study a millicharged co-interacting dark matter scenario, where the primary dark matter constituent is the dark photon A′ and the secondary component is the fermion χ. In this model, χ interacts with A′ via a U(1)′ interaction while being millicharged with respect to normal photons. Our investigation focuses on the oscillation of A′ dark matter into photons within the background of χ particles, revealing that the A′ − χ scattering rate benefits from a Bose enhancement of the A′ final state. As the oscillation production rate is directly linked to the scattering rate, the conversion of A′ dark matter into monochromatic photons experiences significant amplification owing to this Bose enhancement, especially when the scattering rate Γsca approaches the dark photon mass mA′\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {m}_{A^{\\prime }} $$\\end{document}. These converted monochromatic photons are detectable through radio telescopes and can induce distortions in the Cosmic Microwave Background (CMB) spectrum. We find that the sensitivity of radio telescopes and the constraints imposed by CMB distortion on the kinetic mixing parameter are notably heightened compared to scenarios without the subdominant millicharged dark matter.

Complete biodegradation of glyphosate with microbial consortium YS622: Structural analysis, biochemical pathways, and environmental bioremediation

The large-scale use of glyphosate has led to the continuous accumulation of residues in the environment, disrupting ecological balance and posing a threat to human health. The main objective of this study was to investigate the potential role of microbial consortium YS622 for the bioremediation of glyphosate-contaminated water/soil environments. YS622 could degrade 100 % of 50 mg/L glyphosate within 36 h, an efficiency higher than that of any other consortia or pure microorganisms reported so far. The kinetic parameters of maximum specific degradation rate, half-rate constant, and inhibition coefficient were determined to be 0.2 h−1, 139.0 mg/L, and 25.1 mg/L, respectively. YS622 metabolized glyphosate via the aminomethylphosphonic acid pathway via breaking the C–N bond. In addition, the sequencing analysis revealed that Azospirillum, Cloacibacterium, and Ochrobactrum were the dominant genera of YS622 in the degradation process, indicating that these genera might play pivotal roles in glyphosate biodegradation. Furthermore, the inoculation of YS622 in both sterilized and unsterilized water–sediment systems significantly promoted the degradation of glyphosate, with over 97 % degradation of 60 mg/L glyphosate within 36 h. The discovery of YS622 fills a gap in the synergistic metabolism of glyphosate at the community level and provides a potential candidate for bioremediation applications.

ESR-thermochronometry of the MIZ1 borehole, Tono, Japan

Previous studies have shown that the low-relief Tono region (Japan) underwent Quaternary exhumation at rates of <1 mm yr-1. Here we explore whether electron spin resonance (ESR) signals of quartz from six samples from the MIZ1 borehole can resolve such low rates of exhumation, or whether the samples are in thermal equilibrium with ambient borehole temperature. ESR thermochronometry requires that both sample-specific signal saturation and thermal decay are constrained in the laboratory, which makes measurements highly time-consuming. To overcome this, the development of a standardised growth curve (SGC) was explored, which allowed more rapid constraint of the trapped-charge concentrations of each of the samples. Thermal kinetic parameters were determined using an isothermal decay experiment for each individual sample and except for sample MIZ1-01, it was possible to fit all the isothermal decay data together to yield a single set of kinetic parameters that successfully described the dataset. Using a single set of kinetic parameters also allows faster measurement. The ESR thermochronometry results show that the MIZ1 samples are not in thermal equilibrium, but rather reflect ongoing exhumation in this region. Exhumation rates determined from the Al-centre are consistent with existing thermochronometric data and indicate total exhumation of 385 ± 220 m over the past 1 Myr. In contrast the different Ti-centre options (A, B, D) yield a total exhumation of ∼1 km over the same period. The cause of this discrepancy is unclear but may relate to sub-linearity of Ti-centre dose response, that lead to underestimation of the trapped-charge concentration and hence an overestimation of exhumation rates. Our results indicate that ESR-thermochronometry can be successfully applied in low-relief zones undergoing exhumation at rates <1 mm yr-1, and that an SGC and common thermal kinetic parameters may be used to expediate sample measurements.

Development and fabrication of graphene oxide and reduced graphene oxide incorporated MnFe2O4@Bi2WO6 nanocomposite for efficient degradation of antibiotic drug as water contaminant under visible-light illumination

Tetracyclines are one category of extensively applied antibiotics. Meantime, owing to misapplication and inappropriate disposal, they are mostly discovered in wastewater, which causes a series of environmental contamination and stated a threat to a person's health and security. The present study investigates the photodegradation of tetracycline using MnFe2O4@Bi2WO6/graphene oxide, GO, and MnFe2O4@Bi2WO6/reduced graphene oxide, RGO, and MnFe2O4@Bi2WO6 nanocomposites as permanent photocatalyst with the aid of visible light. A facile microwave assisted combustion method was applied in solid state rapidly, conveniently to fabricate MnFe2O4@ Bi2WO6–GO and MnFe2O4@ Bi2WO6–rGO nanocomposites at low power 150 W and in time 10 min with very low amount of glycine (as fuel). Consequently, XRD, EDX Mapping, DRS, PL, TEM, FESEM, FTIR, VSM, BET and UV–Visible spectrophotometric analysis demonstrated characteristic of nanocomposites and specifications of existent photocatalyst. Magnetic investigations revealed that the MnFe2O4@ Bi2WO6-GO and MnFe2O4@ Bi2WO6–RGO nanocomposites can be easily separated from the solution by an external magnetic field. MnFe2O4@ Bi2WO6–GO nanocomposites were discovered with high specific surface area 73.83 m2/g than MnFe2O4@Bi2WO6–RGO nanocomposites with specific surface area 17.75 m2/g. Highest photocatalytic activity was determined for the MnFe2O4@ Bi2WO6–GO (catalyst-0.10 g/l, tetracycline antibiotic concentration 10 mg/l and at pH = 4) within 25 min of visible light irradiation without using any oxidizing agent. The investigation of kinetic study revealed that kinetic parameter specified to photodegradation and experimental outcomes follow first-order model. the superoxide, hydroxyl radicals, ℎ+ holes and light are the principal demonstrates of the reaction mechanism for the effective degradation of tetracycline drug. The evaluation of MnFe2O4@ Bi2WO6–GO and MnFe2O4@ Bi2WO6–RGO magnetic catalysts has proposed the encouraging and significant role of nanocomposites in perilous pharmaceuticals refinement from industrial wastewater and also, magnetically photocatalyst attributes can be used as a potent separable tool for eliminating water pollution problems in the various industry.

Thermoluminescence and Kinetic Parameters of Beta Rays Irradiated Egyptian Muscovite.

The current work was going to study the dosimetric properties of Egyptian muscovite minerals irradiated with β-rays using the thermoluminescence technique (TL). The analysis of the TL glow curves was done using the (Tm - Tstop) and the initial rise methods. The deconvolution of the muscovite glow curves was analyzed to have eight superimposed trapping peaks. These trapes were located at 0.72, 0.80, 0.98, 1.09, 1.19, 1.30, 1.50, and 1.59 eV. Muscovite samples were studied at doses up to 330 Gy and exhibited good linearity in relation to beta radiation. The kinetic parameters, sensitivity, and dosimetric characteristics were evaluated. High accuracy was achieved through the repeatability of TL measurements.

Cerebral and myocardial kinetics of [11C]acetoacetate and [11C]β-hydroxybutyrate: A comparative crossover study in healthy rats

BackgroundKetone metabolism has been studied using positron emission tomography (PET) with the radiotracers [11C]acetoacetate and [11C]β-hydroxybutyrate. However, whether these two radiotracers actually yield equivalent estimates of cerebral and myocardial ketone metabolism has not yet been investigated. This study aimed to investigate and compare the kinetics of both tracers in the brain and heart of healthy rats under varying levels of circulating ketones at baseline and after a single-dose exogenous ketone ester (KE) supplement. MethodsSix healthy Sprague-Dawley rats each underwent two scans with each tracer: one following oral KE administration and one with a placebo. Cerebral kinetic parameters (Ki, VT, and cerebral metabolic rate (CMR)) were obtained using the Patlak method, whereas myocardial kinetic parameters (K1, k2, and VT) were derived using a 1-tissue compartment model. Parameters were compared through mixed-effects, correlation, and Bland-Altman analyses. ResultsGlobal CMR increased 3–4-fold in the KE group versus placebo, with strong positive correlations between CMR and plasma ketone levels for both tracers. Correlations between [11C]acetoacetate and [11C]β-hydroxybutyrate were moderate and non-significant for relative cerebral uptake expressed as Ki (ρ = 0.40) and for VT (ρ = 0.38) but strongly positive for absolute uptake, CMR (r = 0.84), with a non-significant mean bias of −0.03. In contrast, myocardial kinetics showed only non-significant weak to moderate correlations between the radiotracers (K1 (r = 0.04), k2 (r = −0.27), and VT (ρ = 0.43)), with no systematic biases. Conclusion[11C]acetoacetate and [11C]β-hydroxybutyrate can be used interchangeably for measuring global CMR in healthy rats but differ in certain cerebral and myocardial kinetics. Whether these findings are generalizable to pathological conditions warrants further studies to explore the kinetics of these tracers in disease models.

Damage to Mitochondria During the Cryopreservation, Causing ROS Leakage, Leading to Oxidative Stress and Decreased Quality of Ram Sperm.

Semen cryopreservation can achieve long-term preservation of sperm. Ice crystal damage, as well as oxidative stress, result in mitochondrial dysfunction and a reduction in sperm motility after thawing. However, limited information exists regarding the impact of reactive oxygen species (ROS) and mitochondria on the cryopreservation of ram sperm. The primary objective of this study was to investigate the relationship between ROS and mitochondria concerning sperm quality during the cryopreservation of ram sperm. This investigation assessed sperm motility, kinematic characteristics, membrane integrity, acrosome integrity, mitochondrial membrane potential (MMP), adenosine triphosphate (ATP) levels, expression of mitochondrial respiratory genes (NDUFV2, SDHA, CYC1, and COXIV), ROS levels, malondialdehyde (MDA) content, phosphatidylserine externalisation rate, sperm ultrastructure, mtDNA copy number, expression of apoptosis-related genes (Bax, Caspase-3, and Caspase-8), Cytochrome C, and Caspase-3 content. The results showed the cryopreservation significantly (p < 0.05) decreased motility, kinetic parameters, membrane integrity, acrosome integrity, MMP, ATP, mRNA expression levels of mitochondrial respiratory-related genes, and significantly (p < 0.05) increased ROS levels, MDA content, phosphatidylserine externalisation rate, damage of sperm ultrastructure, mtDNA copy number, mRNA expression levels of apoptosis-related genes, Cytochrome C and Caspase-3 content compared to the fresh semen group. In conclusion, the cryopreservation causes damage to mitochondria, leading to increased ROS and subsequent oxidative stress. This process also initiates mitochondrial dysfunction and interferes with the electron transport chain, ultimately resulting in decreased MMP and ATP production. Furthermore, the liberation of Cytochrome C prompted the increase in Caspase-3 expression and subsequent sperm apoptosis occurred, ultimately leading to a deterioration in sperm quality after thawing.

Thermoluminescence and Apollo 17 ANGSA Lunar Samples: NASA's Fifty‐Year Experiment and Prospecting for Cold Traps

AbstractBy placing Apollo 17 regolith samples in a freezer, and storing an equivalent set at room temperature, NASA effectively performed a 50‐year experiment in the kinetics of natural thermoluminescence (TL) of the lunar regolith. We have performed a detailed analysis of the TL characteristics of four regolith samples: a sunlit sample near the landing site (70180), a sample 3 m deep near the landing site (70001), a sample partially shaded by a boulder (72320), and a sample completely shaded by a boulder (76240). We find evidence for a total of eight discrete TL peaks, five apparent in curves for samples in the natural state and seven in samples irradiated in the laboratory at room temperature. For each peak, we suggest values for peak temperatures and the kinetic parameters E (activation energy, i.e. “trap depth,” eV) and s (Arrhenius factor, s−1). The lowest natural TL peak in the continuously shaded sample 76240 dropped in intensity by 60 ± 10% (1976 vs. present room temperature samples) and 43 ± 8% (freezer vs. room temperature samples) over the 50‐year storage period, while sunlit and partially shaded samples (70001, 70180, 72321, 72320) showed no change. These results are consistent with the E and s parameters we determined. The large number of peaks, and the appearance of additional peaks after irradiation at room temperature, and literature data, suggest that glow curve peaks are present in lunar regolith at ∼100 K and their intensity can be used to determine temperature and storage time. Thus, a TL instrument on the Moon could be used to prospect for micro‐cold traps capable of the storage of water and other volatiles.