Reactivity Characteristics Research Articles

Effects of Tube Diameter and Gas Flow Rate on the Discharge Dynamics Characteristics and Reactive Species of Nanosecond Pulsed Discharge Plasma in Contact With Water

ABSTRACTThe use of millimeter quartz tubes to generate non‐thermal plasma in contact with liquid is widely applied in medicine, such as the effective disinfection of catheter tubes and tooth cavities. Here, the effects of tube diameter and gas flow rate on discharge dynamics and reactive species characteristics of nanosecond pulse needle‐water discharge are studied using an ICCD camera and optical emission spectra. The discharge diffusion is increased significantly by an appropriate combination of tube diameter and gas flow rate. Besides, the discharge intensity, emission spectra intensities of reactive species, gas temperature, and electron density increase with the increase of quartz tube diameter and gas flow rate, which contributes to enhance the production of OH and H2O2 species in aqueous samples.

Enhancing the diffusion capabilities of oxygen ions and hydrogen protons in Protonic Ceramic Fuel Cells at intermediate temperatures through doping material and ratio adjustments

Abstract This study aims to investigate the changes in the diffusion capabilities of oxygen ions and hydrogen protons within the electrolyte materials of Protonic Ceramic Fuel Cells (PCFC) under various doping materials, doping ratios, and temperature effects. It utilizes molecular dynamics methods combined with the ReaxFF force field to analyze the reactivity and transport characteristics of oxygen ions and hydrogen protons in the BZY (Yttria-doped barium zirconates) microstructure of PCFCs. The research finds that for intermediate temperature ranges (573K-773K), the optimal doping ratio of Y2O3 is 13.6%, and at an operating temperature of 673K, using MgO as a doping material for BZY can enhance the diffusion coefficient of hydrogen protons in the electrolyte, thereby optimizing the performance of PCFC.

ω‐Aminomethyl Longifolene Amide Derivatives: Synthesis, Crystal Structure, Hirshfeld Surface, DFT, Antimicrobial, and Molecular Docking Studies

AbstractTwelve novel ω‐aminomethyl longifolene amide derivatives (6 a–6 l) were synthesized and characterized. The intermolecular contacts and the relationship of structure‐property for the synthesized compounds were performed with the use of two‐dimensional fingerprint plots and Hirshfeld surface method. Moreover, the chemical reactivity and geometrical characteristics of target compounds were investigated using density functional theory (DFT) method. Molecular docking studies were performed to investigate the interactions between compounds 6 a–6 l and sortase A (SrtA) from S. aureus, the carboxy terminal domain of colicin E5 (E5‐CRD) and Serine/Threonine phosphatase Z1 (PPZ1) from C. albicans, respectively, and together with their biological activities. The docking results of the synthesized compounds 6 a–6 l showed different binding efficiencies and inhibitory effects on S. aureus, E. coli and C. albicans. Furthermore, preliminary antimicrobial activity assay showed that compounds 6 f, 6 i and 6 k exhibited comparable or superior antibacterial activity against S. aureus, B. subtilis and K. pneumoniae compared to rifampicin with minimum inhibitory concentration (MIC) values from 0.488 to 0.977 μg/mL. In addition, the absorption, distribution, metabolism and excretion (ADME) and drug‐likeness properties of the synthesized derivatives were evaluated as well.

Enhanced Corrosion Resistance of Ag Electrode Through Ionized 2‐Mercaptobenzothiazole in Inverted Perovskite Solar Cells

AbstractThe utilization of Ag electrodes in inverted perovskite solar cells (PSCs) is prevalent; however, their inherent reactivity and corrosive characteristics toward perovskite materials often lead to significant stability concerns. Here, 1‐ethyl‐3‐methyl‐1h‐imidazolium 2‐mercaptobenzothiazole (EM) ionic liquid is designed and introduce it into the bathocuproine (BCP) barrier layer to mitigate the potential chemical corrosion of the Ag electrode by the perovskite layer. EM forms multiple interaction modes through the coordination of two types of bonds, C─N, C═N, and C─S, and chelation with Ag, resulting in the formation of a dense chemical anti‐corrosion layer on the Ag surface. By raising the Ag electrode's corrosion potential and decreasing its corrosion current, the occurrence of chemical reactions and corrosion of the Ag electrode by the perovskite layer is effectively suppressed. Additionally, the ionized EM optimizes the band structure and conductivity of BCP and enhances the electron transfer capability at the electron transport layer/Ag interface. The BCP:EM‐based inverted PSCs exhibit an efficiency of 25.11% and excellent stability. Under continuous operation at 45 °C and one sun illumination, the encapsulated device maintains 85.6% of its initial efficiency after 1000 h at the maximum power point.

Unveiling the adsorption mechanism of propanehydrazine derivatives on magnesium oxide surface: Insights from computational approach

The use of green and effective inhibitors for preventing metal oxide (MgO) corrosion in industrial applications is highly significant in promoting environmental protection and sustainable development. This study delves into the adsorption behavior and interfacial mechanism of environmentally friendly inhibitor derived from propane hydrazine (PH) on MgO surface. Specifically, PH1, PH2, PH3, and PH4 were explored for their effectiveness in preventing corrosion by using advanced theoretical simulations-based density functional theory (DFT) for assessing the reactivity and adsorption characteristics. The study considered a detailed exploration of local and global reactivity descriptors, providing insights into the inhibitors’ reactivity and adsorption abilities in both isolated and adsorbed states. These findings focus more in the mechanisms underlying organic-inorganic interactions and present promising prospects for further development and application. Using first-principles DFT calculations alongside quantitative molecular surface analyses, we examined the adsorption patterns of PHs on the MgO(100) surface. These investigations are boosted by the application of independent gradient model (IGM) framework, providing robust verification of PHs' adsorption behavior on MgO(100) surface. Our calculations reveal a substantial decrease in the energy gap following complex formation, suggesting that charge density changes occur upon interaction with MgO surfaces, thereby facilitating direct electron transfer in all the studied systems. Noreover, the results highlight the crucial role of intermolecular interactions in boosting the interaction between PHs and the [Mg(H2O)6]2+ cation. First-principles DFT calculations show that all PH molecules consistently display parallel adsorption on the MgO surface, where the oxygen atoms form bonds with adjacent magnesium atoms. The bond lengths vary from 2.18 to 2.35 Å when PHs bind to the Mg atoms in parallel orientations through the oxygen atom, suggesting a stable parallel arrangement for PH molecules on the MgO surface. The calculated adsorption energy (Eads) varies in the following order: MgO-PH3 (−815.14 Kcal mol−1) > MgO-PH2 (−803.85 Kcal mol−1)) > MgO-PH4 (−695.38 Kcal mol−1) > MgO-PH1 (−125.77 Kcal mol−1). This trend indicates that parallel interactions enhance the adsorption behavior and binding of PH compounds through inter- and intra-molecular interactions, resulting in the PHs being centered at specific sites on the MgO surface. The potential enhancement in electrochemical properties is believed to stem from the synergistic interaction between the PHs and the MgO surface, which theoretically allows for a precise adjustment of their adsorption and interaction within the composite structure. This understanding provides a fundamental framework for examining the complex interfacial dynamics between inhibitor structures and elucidating how these molecular interactions influence the selection of corrosion inhibitors and their adsorption behaviors on the corrosion layer's surface, rather than on metallic Mg.

Synthesis, antimicrobial activity and computational studies on (E)-N-(2((4-chlorobenzylidine)amino)ethyl)napthalen-1-amine

The novel Schiff bases were synthesized by combining N1-(Napthalen-1-yl)ethane 1,2-diamine with chlorine-substituted benzaldehyde. The compound is designated as (E)-N-(2((4-chlorobenzylidine)amino)ethyl)napthalen-1-amine (4CLB). This structure was verified by experimental techniques including infrared, NMR, fluorescence, UV, and theoretical methods. Using the B3LYP functional the titled compound computational study was executed. The results for infrared and NMR analysis of the molecule exhibited a significant degree of agreement in both observed and simulated. The reactivity characteristics of 4CLB were computed. The microbiological efficacy of the compound was assessed against multiple Gram-positive bacteria S. aureus, S pneumonia, and Bacillus subtilis. The compound was tested against the following Gram-negative bacteria: Klebsiella pneumonia, E coli, and Proteus vulgaris. The compound Schiff base exhibits the most effective antibacterial activity against all microbes. The 4CLB compound quantum calculations have a strong correlation with antibacterial activity. The compound has non-covalent Hydrogens, these Hydrogens are bonded with the corresponding proteins. It is checked by molecular docking in the Auto Dock software.

Microstructure and energy release properties of W-Zr-Al energetic structural material fabricated by explosive consolidation

Multi-element intermetallic energetic structural materials (ESMs) as a new typical ESMs characterized by their high heat release properties and strength, which could be applied as reactive fragment, reactive shell and reactive shaped charge. Al-based ESMs had been extensively studied due to their excellent mechanical properties and high energy release characteristics. But, the low density of Al-based ESMs hindered its application. However, the need for higher density and energy release persists. In this work, the nearly fully dense W-Zr-Al ESMs with a molar ratio of 1.9:1:1 was fabricated successfully by explosive consolidation. The density reached 10.12 g/cm3 (97.5 % of the theoretical maximum density). Microstructure of the specimen was characterized by X-ray diffractometer (XRD), optical microscopy (OM), scanning electron microscope (SEM), energy dispersive spectrometry (EDS) and transmission electron microscope (TEM). The heat treatment was used to further improve the performance of the specimen and the mechanical properties of quasi-static compression was investigated before and after heat treatment. The reaction activity and process of W-Zr-Al ESMs was discussed by differential scanning calorimetry (DSC). Besides, the impact-induced energy release tests were carried out to evaluate the reactive characteristics of the W-Zr-Al ESMs. The results indicated that high-density, good-strength and high energy release unreacted W-Zr-Al energetic materials were fabricated successfully by explosive consolidation.

Comprehensive thermal properties, kinetic, and thermodynamic analyses of biomass wastes pyrolysis via TGA and Coats-Redfern methodologies

This study comprehensively analyzes the thermal decomposition characteristics as well as the kinetic and thermodynamic parameters of five biomass wastes, including coffee husk, groundnut shell, macadamia nutshell, rice husk, and tea waste, using Thermogravimetric Analysis (TGA) and the Coats-Redfern method. The TGA experiments were conducted on a PerkinElmer STA 6000 instrument under an inert N2 atmosphere with a heating rate of 20 °C/min, spanning a temperature range from 25 °C to 950 °C. The results identified three distinct pyrolysis stages: drying, devolatilization, and char formation, with macadamia nutshell demonstrating the highest thermal reactivity and efficient devolatilization characteristics, reflected by its lowest initial devolatilization temperature (175 °C) and highest peak temperature (380 °C). Kinetic analysis revealed that coffee husk had the highest overall activation energy (Ea) of 60.59 kJ/mol, indicating complex thermal degradation behavior. The thermodynamic evaluation showed that coffee husk also exhibited the highest enthalpy change (ΔH=55.46 kJ/mol) but the lowest Gibbs free energy change (ΔG=148.34 kJ/mol), suggesting high energy requirements for decomposition but relatively more spontaneous reactions compared to other biomass types. Macadamia nutshell demonstrated high ΔG (163.24 kJ/mol) and moderate ΔH (32.44 kJ/mol), reflecting greater resistance to spontaneous decomposition. The comprehensive pyrolysis index (CPI) and devolatilization index (Ddev) confirmed macadamia nutshell as the most reactive biomass, while rice husk exhibited the lowest reactivity. The findings highlight the importance of multi-step kinetic analysis for accurately understanding pyrolysis processes, providing critical insights for optimizing biomass conversion for energy production. Future research should explore co-pyrolysis with varied biomass mixtures and advanced kinetic modeling to enhance energy yields.

Synergy Effect of High K-Low Ca-High Si Biomass Ash Model System on Syngas Production and Reactivity Characteristics during Petroleum Coke Steam Gasification

The synergy effect of high K-low Ca-high Si biomass ash-based model system (BAMS) on the synthesis gas output and reaction characteristics of petroleum coke (PC) steam gasification process was studied using three biomass ash (BA) components, KCl, SiO2, and CaCO3, which were used as the model compounds. In the ternary model system, the steam gasification experiment of PC was conducted using a fixed bed reactor and gas phase chromatography. The synergistic effects of binary and ternary components in the ternary model system on the gasification of PC were obtained. These investigations were based on the data from the gas analysis and examined the gasification reaction process, syngas release behavior, and reaction characteristics. This study examined the effects of binary and ternary components in the ternary model system on the evolution of semi-char structure during PC gasification. This correlation revealed the synergistic effect of the model system on PC gasification. Scanning electron microscope (SEM) and Raman spectroscopy were used to characterize the structure and surface microstructure of the gasification semi-char. The results showed that the yields of different gases in the ternary model system were in H2 > CO > CO2. Compared with single PC gasification, the yields of H2, CO, syngas, and carbon conversion were increased by 29.42 mmol/g, 20.40 mmol/g, 56.68 mmol/g, and 0.35, respectively. All other components in the ternary model system with high K-low Ca-high Si demonstrated catalytic effect, except for SiO2 and the Ca-Si system, which showed inhibitory effects on syngas release and reaction features. Integrating SEM and Raman spectroscopic analyses, it was elucidated that CaCO3 and KCl diminished the degree of graphitization in semi-char through interactions with the carbonaceous matrix. This phenomenon facilitated the gasification process and exhibited a synergistic effect. Secondly, SiO2 will react with CaCO3 and KCl, producing inert silicates and inactivating these compounds, leading to the decline of catalysis.

A second-order kinetic model for global analysis of vibrational polariton dynamics.

The interaction between cavity photons and molecular vibrations leads to the formation of vibrational polaritons, which have demonstrated the ability to influence chemical reactivity and change material characteristics. Although ultrafast spectroscopy has been extensively applied to study vibrational polaritons, the nonlinear relationship between signal and quantum state population complicates the analysis of their kinetics. Here, we employ a second-order kinetic model and transform matrix method (TMM) to develop an effective model to capture the nonlinear relationship between the two-dimensional IR (or pump-probe) signal and excited state populations. We test this method on two types of kinetics: a sequential relaxation from the second to the first excited states of dark modes, and a Raman state relaxing into the first excited state. By globally fitting the simulated data, we demonstrate accurate extraction of relaxation rates and the ability to identify intermediate species by comparing the species spectra with theoretical ground truth, validating our method. This study demonstrates the efficacy of a second-order TMM approximation in capturing essential spectral features with up to 10% excited state population, simplifying global analysis and enabling straightforward extraction of kinetic parameters, thus empowering our methodology in understanding excited-state dynamics in polariton systems.

Herpes virus reactivation induced by abrocitinib: A real-world pharmacovigilance analysis of the FDA Adverse Event Reporting System (FAERS) database

PurposeLarge real-world studies evaluating the association between abrocitinib and herpes virus reactivation are lacking. This objective of investigation was to delineate the characteristics of abrocitinib-associated herpes virus reactivation through the FDA Adverse Event Reporting System. ResultsTotal of 56 reports were distinctly associated with herpes virus reactivation, with serious adverse events accounting for 67.86 %. Several noteworthy findings emerged: (1) female is associated with relatively high risk of herpes virus reactivation. (2) The proportion of herpes virus reactivation cases reported from the United States has decreased significantly compared to the overall reports. (3) The inclusion of dupilumab in combination regimens appeared to be associated with a comparatively reduced risk of herpes virus reactivation, while the risk of regimens containing baricitinib was increased. ConclusionThese findings will help us to identify risk factors for herpes virus activation in atopic dermatitis patients, and facilitate the implementation of targeted measures to prevent and mitigate herpes virus activation.

Variation of surface property of dodecyl dimethyl betaine modified γ-C2S caused by carbonation: Experimental and DFT simulation studies

The variation of dodecyl dimethyl betaine (DDB) on the surface properties of γ-dicalcium silicate (γ-C2S) was investigated through experimental and density functional theory approaches. The study also investigated the influence of DDB content on carbonation reactivity, carbonation products, and carbonation hardening characteristics. The results demonstrate that DDB can elevate the carbonation temperature of γ-C2S and enhance the dissolution of calcium ions, thereby promoting its carbonation activity. The appropriate content of DDB can enhance the dense aggregation of calcite on the surface of uncarbonated γ-C2S, thereby contributing to the densification and strength development of the matrix. DDB decreases the surface energy of γ-C2S and enhances its surface activity. Moreover, the (010) surface exhibits the lowest surface energy, facilitating the occurrence of robust chemical interactions and carbonation reactions. The enhancement mechanism of the carbonation reaction is associated with the interaction between carbonyl oxygen in DDB and surface calcium. There is a complexation between the two, which promotes the reaction with CO2. The results of this study possess significant implications for the selection of additives employed in modifying the surface properties of calcium silicate minerals and facilitating carbonation reactions.

Reactor core design with enriched gadolinia burnable absorbers for soluble Boron-Free operation in the innovative SMR

Effective strategies for maintaining reactor reactivity at a consistent level are indispensable to enable soluble boron-free (SBF) operation in innovative small modular reactor (i-SMR) operation. This paper presents a reactor core design tailored for SBF operation in i-SMR, utilizing concentrated gadolinia burnable absorber rods. This investigation evaluates the concentration range of 155,157Gd and its reactivity characteristics, which are crucial for sustaining excess reactivity. The viability of employing enriched 155,157Gd for the i-SMR SBF operation is established through comprehensive analysis and simulations. Moreover, integrating 155,157Gd with integral gadolinia burnable absorber rods enhances the reactivity control and operational adaptability. Leveraging the spatial self-shielding effect of gadolinia extends the reactivity management capabilities and ensures the operational performance of the i-SMR as optimizing the cycle length. Core design considerations encompassing FA configurations and control rod patterns are investigated to ensure safety and performance across the initial and reload cycles. The feasibility of the SBF operation is verified by assessing compliance with the top-tier requirements of the i-SMR, thus underlining its potential for practical implementation.

Clathrate Hydrates as a Kind of Promising Ice Nanoreactors.

Since their discovery, clathrate hydrates (CHs) have received great attention both from theoretical and experimental aspects due to their great potential for gas storage and prospective applications as icy crystal materials. However, there has been limited research on the decomposition, reduction or other reactions of gases enclosed in CHs. Thanks to their unique hydrogen bonding network and cavity structures, CHs can serve as the promising nanoreactors to achieve chemical conversions, e. g. reducing greenhouse gases. In this review-type article, we characterize the potential performance of such CHs nanoreactors by discussing their multiple functions including important roles of hydrogen bonds in CHs, e. g. the confinement effect and proton source, and then discuss the enhanced electron-binding ability of guest molecules and the structures and properties of trapped electrons in the stacked nanocages, which contribute to our understanding of chemical reactions occurring in CHs. Finally, we provide detailed analyses of representative reaction mechanisms underwent in CH nanoreactors and effective calculational and molecular dynamics simulation methods. This review-type article aims to provide a detailed summary about the functional characteristics of CHs and reactivity in CHs, which make CHs a kind of promising icy nanoreactors.

Analysis of effects of inlet air and fuel conditions on reactive flow characteristics in a gas turbine model combustion chamber

Analysis of effects of inlet air and fuel conditions on reactive flow characteristics in a gas turbine model combustion chamber

Design, synthesis, biological evaluation, and molecular modeling simulations of new phthalazine-1,4-dione derivatives as anti-Alzheimer's agents.

The development of targeted phthalazine-1,4-dione acetylcholinesterase (AChE) inhibitors for treating Alzheimer's disease involved the synthesis of 32 compounds via a multistage process. Various analytical techniques confirmed the compounds' identities. Thirteen compounds were found to inhibit AChE by more than 50% without affecting butyrylcholinesterase (BChE). Among these, three compounds, 8m, 8n, and 8p, exhibited extraordinary activity similar to donepezil, a reference AChE inhibitor. During enzyme kinetic studies, compound 8n, displaying the highest AChE inhibitory activity, underwent evaluation at three concentrations (2 × IC50, IC50, and IC50/2). Lineweaver-Burk plots indicated mixed inhibition activity for compound 8n against AChE, suggesting a combination of competitive and noncompetitive characteristics. Additionally, effective derivatives 8m, 8n, and 8p exhibited high blood-brain barrier (BBB) permeability in in vitro parallel artificial membrane permeability assay tests. Molecular docking studies revealed that these compounds bind to the enzyme's active site residues in a position similar to donepezil. Molecular dynamic simulations confirmed the stability of the protein-ligand system, and the chemical reactivity characteristics of the compounds were investigated using density functional theory. The compounds' wide energy gaps suggest stability and therapeutic potential. This research represents a significant step toward finding a potential cure for Alzheimer's disease. However, further research and testing are required to determine the compounds' safety and efficacy. The unique structure of phthalazine derivatives makes them suitable for various biological activities, and these compounds show promise for developing effective drugs for treating Alzheimer's disease. Overall, the development of these targeted compounds is a crucial advancement in the search for an effective treatment for Alzheimer's disease.

Valorization of a high-sulfur petroleum coke for energy and fuels through its co-processing with a forest waste, using concrete wastes for sulphur and carbon dioxide capture under mild conditions

Current work provided a comprehensive assessment on the pyrolysis, combustion and gasification of a high-sulfur pet coke (PEC) and its blends with a forest waste (FOP). The potential of waste concrete fractions to capture SO2 and CO2 emissions was explored. The experiments were conducted in a fixed bed system and a thermogravimetric-mass spectrometric unit. Thermal behavior, reactivity, conversion, synergy, structural and chemical characteristics of solid materials, quantitative analysis of products and heating value, chemical, mineralogical and fusibility analysis of ashes were studied as a function of temperature, blending ratio and sorbent/fuel ratio. Addition of sorbent at a ratio Ca/S = 2 resulted in a desulfurization extent of 76–81 % during combustion. Quarry dust sorbent captured up to 95.4 % of CO2 emitted below 700 °C. At 1000 °C H2 content was 64.8–72.9 % mol and syngas yield 1.1–1.8 m3/kg. The gasification performance of PEC was improved upon blending with FOP.

Recent Progress in Synthetic and Biological Application of Diorganyl Diselenides.

Diorganyl diselenides have emerged as privileged structures because they are easy to prepare, have distinct reactivity, and have broad biological activity. They have also been used in the synthesis of natural products as an electrophile in the organoselenylation of aromatic systems and peptides, reductions of alkenes, and nucleophilic substitution. This review summarizes the advancements in methods for the transformations promoted by diorganyl diselenides in the main functions of organic chemistry. Parallel, it will also describe the main findings on pharmacology and toxicology of diorganyl diselenides, emphasizing anti-inflammatory, hypoglycemic, chemotherapeutic, and antimicrobial activities. Therefore, an examination detailing the reactivity and biological characteristics of diorganyl diselenides provides valuable insights for academic researchers and industrial professionals.

Varicella-Zoster Virus Reactivation After Pediatric Allogeneic Hematopoietic Stem Cell Transplantation, Single-Center Experience of Acyclovir Prophylaxis.

Varicella-zoster virus (VZV) reactivation is the most common infectious complication in the late posthematopoietic stem cell transplantation (HSCT) period and is reported as 16%-41%. Acyclovir prophylaxis is recommended for at least 1 year after HSCT to prevent VZV infections. However, studies on the most appropriate prophylaxis are ongoing in pediatric patients. Patients who underwent allogeneic HSCT between January 1, 1996 and January 1, 2020 were retrospectively analyzed to outline the characteristics of VZV reactivation after allogeneic HSCT in pediatric patients using 6 months acyclovir prophylaxis. There were 260 patients and 273 HSCTs. Median age was 10.43 (0.47-18.38), and 56% was male. Median follow-up was 2325 days (18-7579 days). VZV reactivation occurred in 21.2% (n = 58) at a median of 354 (55-3433) days post-HSCT. The peak incidence was 6-12 months post-HSCT (43.1%). Older age at HSCT, female gender, history of varicella infection, lack of varicella vaccination, low lymphocyte, CD4 count, and CD4/CD8 ratio at 9 and 12 months post-HSCT was found as a significant risk for herpes zoster (HZ) in univariate analysis, whereas history of varicella infection and low CD4/CD8 ratio at 12 months post-HSCT was an independent risk factor in multivariate analysis. Tailoring acyclovir prophylaxis according to pre-HCT varicella history, posttransplant CD4 T lymphocyte counts and functions, and ongoing immunosuppression may help to reduce HZ-related morbidity and mortality.

Sex differences in skin microcirculatory vascular reactivity in experimental lipopolysaccharide-induced endotoxinemia

Bacterial lipopolysaccharide (LPS) plays a leading role in the development of a systemic inflammatory response and endogenous intoxication. However, the sex differences in the functional state of the microcirculatory bed in LPS-induced endotoxinemia have been poorly studied. Objective. To study the characteristics of skin microcirculatory vascular reactivity in experimental LPS-induced endotoxinemia in male and female rats. Material and methods. Modeling of endotoxinemia was performed by intraperitoneal injection of LPS of the cell wall of the bacterium Salmonella enterica to male and female Wistar stock rats. Two doses of LPS were used: 50 mg/kg and 10 mg/kg. We used laser Doppler flowmetry to evaluate skin perfusion before and after LPS injection, blood flow changes under test conditions with local contact hypothermia caused by a thermoelement. Results. 48 hours after LPS injection, a decrease in blood flow was observed, especially pronounced at a dose of LPS 50 mg/kg. During the test with local cooling of the skin, a change in the kinetics of the reaction was noted. Blood flow reduction was 75% (LPS 50 mg/kg) and 51% (LPS 10 mg/kg), statistically significantly different from the control groups. At the same time, the classic phenomenon of “cold vasodilation” observed in control rats was absent in all groups with the injection of LPS. Maximum perfusion after restoration of blood flow in females was achieved 3 times faster than in males (LPS 10 mg/kg). Conclusion. In experimental LPS-induced endotoxinemia, a dose-dependent decrease in skin perfusion was revealed. We obtained new data on the absence of pronounced “cold vasodilation” at local contact hypothermia. The results of the study indicate a violation of the mechanisms of neurogenic vasoconstriction and endothelium-dependent vasodilation, reflecting systemic disorders of microcirculation regulation. At the same time, the females showed a more positive dynamics of blood flow restoration in the test with local cooling of the skin, indicating a greater functional reserve and a more effective mechanism of autoregulation of the blood microcirculation system. A functional test with local contact cooling of the skin is highly informative for assessing vascular reactivity and preservation of the autoregulation mechanism of microcirculation in modeling endogenous intoxication