Activation Processes Research Articles

Preparation of amorphous coal-based activated coke via a two-step process of carbonization and steam activation

The coal-based activated coke (AC) is suitable for desulfurization and denitrification in coal-fired power plants. However, the current studies on millimeter-sized amorphous AC are limited. To evaluate the preparation parameters of millimeter-sized amorphous AC, two typical middle-low rank coal samples, Fugu coal and Datong coal, are selected as the raw materials. The effects of carbonization/activation parameter, particle size and steam flow rate on the yield and pore structure of AC are studied. Samples are analyzed by the synchronous thermal analyzer and the fully automatic rapid specific surface and porosity analyzer. The results show that carbonization and the long-time steam activation at a low temperature can make the internal pores of samples fully developed, significantly increasing the specific surface area and pore volume. The coke yield, specific surface area and mesoporous proportion of Fugu AC obtained by activation at 700 °C for 3 h are 60.95 %, 429.54 m2/g and 29.60 %, respectively. The corresponding values of Datong AC obtained at 850 °C for 3 h are 53.19 %, 892.20 m2/g and 23.01 %, separately. Both of Fugu AC and Datong AC belong to the hierarchical porous AC. The influence of particle sizes on the performance of AC at the millimeter level is within the acceptable range. Therefore, the same carbonization and activation parameters can be chosen to prepare Fugu AC and Datong AC with different particle sizes, respectively. The water vapor flow rate has a significant effect on the pore structure of AC. There is a moderate flow rate (0.03 mL min−1 at this study’s experimental conditions) for preparing the hierarchical porous amorphous AC. The study shows that it is feasible to prepare the amorphous AC with the hierarchical pore structure by employing the millimeter-sized medium–low rank coal particles. The AC could be applied for the pollutants removal in the coal-fired power plants.

Thermodynamic and structural investigation of oily wastewater treatment using peach kernel and walnut shell based activated carbon.

Despite the many articles about activated carbon with different precursors in adsorption process, no in-depth research has been carried out to understand the causes of the difference in surface adsorption characteristics of activated carbon with different precursors and different activation processes. In this work, the ability of two active carbon adsorbents made of walnut shell and peach kernel by two chemical and physical methods (totally 4 different types of activated carbon) in treatment of oily wastewater including diesel, gasoline, used oil or engine lubricant has been compared. The results show that the chemical activated peach carbon active with 97% hardness has provided the highest hardness and physical activated walnut carbon active has obtained the lowest hardness value (87%). It is also found that peach activated carbon has a higher iodine number than walnut activated carbon, and this amount can be increased using chemical methods; Therefore, the highest amount of Iodine Number is related to Peach activated carbon that is made by chemical method (1230 mg/g), and the lowest amount of iodine number is seen in walnut activated carbon that is made by physical method (1020 mg/g). moreover, the pore diameter of physical activated carbon is lower than chemical activated carbon in all cases. So that the pore diameter of chemical activated peach carbon active is equal to 22.08 μm and the measured pore diameter of physical activated peach carbon active is equal to 20.42 μm. These values for walnut are obtained as 22.74 μm and 21.86 μm, respectively. Furthermore, the temperature and pH effects on the adsorption of different synthesized oily wastewater was studied and it was found that a decrease in adsorption can be seen with an increase in temperature or decreasing the pH value, which can be referred to this fact that the process of adsorption is an exothermic process. Finally, to analyze the compatibility of adsorption isotherms with experimental data and to predict the adsorption process, three different isotherms named Langmuir, Temkin, and Freundlich isotherms were applied and their parameters were correlated. The correlation results show that the Langmuir isotherm had the best correlation in all cases compared to the Freundlich and Temkin isotherms, based on the correlation coefficient, and the calculated R2 values which was greater than 0.99 in all the studied cases.

Hierarchical porous carbon with abundant N/O doping as an anode for zinc ion hybrid supercapacitors

Aqueous zinc-ion hybrid supercapacitors (ZISCs) known for their affordability, stability, and high energy density represent innovative energy storage devices. Porous carbon is usually used as the cathode material of ZISCs, and its structure significantly affects the dual performance of high power density and energy density of ZISCs. Herein, a one-pot carbonization strategy is proposed, eliminating the need for templates, additional heteroatom compounds, and activation processes. By precisely controlling the temperature to optimize the structure and electrochemical performance of carbon materials, we successfully synthesized hierarchical porous carbon materials (NOPC-800) with a high specific surface area of 1545.7 mg, featuring dual doping of 12.3 at% nitrogen and 13.35 at% oxygen. The self-doping of abundant nitrogen and oxygen atoms facilitates the chemical adsorption of ions and accelerates pseudocapacitive reaction kinetics. Leveraging these advantages, ZISCs were assembled using NOPC-800 as the positive electrode and zinc as the negative electrode, showcasing remarkable performance: a specific capacity of up to 121.9 mAh g, an energy density of 97.5 Wh kg, and a power density of up to 16000 W kg. Remarkably, NOPC-800 maintained an excellent capacity retention of 94.9% after 10,000 cycles at a current density of 10 A g. This research paves an innovative and feasible path for the design and advancement of novel heteroatom-rich carbon cathodes.

Structure and morphology of chars and activated carbons obtained from thermal treatment of coal and biomass origin materials, including their wastes: Results from the ICCP Microscopy of Carbon Materials Working Group

This paper describes the evaluation of petrographic textures in char and activated carbon derived from coal, coal by-products and biomass, formed during carbonization and activation processes. This work represents the results of interlaboratory exercises from 2016 to 2022 of the Microscopy of Carbon Materials Working Group in Commission III of the International Committee for Coal and Organic Petrology. The interlaboratory exercises were run on photomicrograph samples. For textural characterization of carbon materials, the existing American Society for Testing and Materials (ASTM) classification system for metallurgical coke was applied. Morphological differences were evaluated in 29 carbon material types, including 22 char samples, and 7 activated carbon (AC) samples obtained experimentally using conventional direct/indirect and microwave heating technologies. This approach gives an extended view on the identification of microporous carbons, and how a certain heat treatment develops a certain optical texture and structure in a raw material. The requested evaluation of carbon materials was related to their porosity, origin, extent, and characteristics, which are particular to each carbon material type. Because carbon matrices can form a wide range of optical textures during heat treatment it is important to demonstrate which carbon occurrences will have a crucial role in industrial applications dominated by adsorption phenomena.The interlaboratory exercises included 17 participants from 14 laboratories. Four sets of digital black and white and colour photomicrographs were distributed, which in total comprised 184 fields of different types of carbon material. The results were evaluated based on four levels: (i) optical texture (isotropic/anisotropic), (ii) optical type and size (punctiform, mosaic, fiber, ribbon, domain), iii) morphology (porous, non-porous/massive), and (iv) particle origin (precursor type).The statistical method applied to evaluate the results was based on “raw agreement indices”. Comparative analyses of the average values of the level of overall agreement showed homogeneity in the results, the mean value was 89%, with a minimum value of 87% and a maximum value of 91% for those who participated in at least three out of four exercises.

PREPARATION AND CHARACTERIZATION OF ADSORBENT FROM WASTE SHEA (Vitellaria paradoxa) NUT SHELL

The activated carbons (adsorbents) prepared in this study, were from Vitellaria paradoxa nut shell following the two steps of carbonization and activation processes using H3PO4 and KOH as activating agents and were labelled as HVP for H3PO4 modified adsorbent and KVP for KOH modified adsorbent. The activated carbons were characterized using standard methods of analysis. Bulk density (g/cm3) of the carbons (HVP and KVP) were 0.72±0.03 and 0.69±0.05, and attrition (%) values of 40.76±0.16 and 42.37±0.23 were obtained for HVP and KVP respectively. Results obtained also depict the presence of carboxyl O-H and C-O groups, and the N-H of amine on the surfaces of the activated carbons. The values of pH point of charge zero (pHzpc) obtained for HVP and KVP were 6.40 and 6.60 and were less than the pH values of 6.78±0.00 and 7.18±0.01 for HVP and KVP respectively. SEM results revealed surfaces with pores with different dimensions in both HVP and KVP. Results of the study suggest that the prepared adsorbents can be effectively applied in wastewater treatment.

Assessment of biomarkers indicating activation of the complement system in pregnant women with fetal growth restriction

Aims: To compare serum levels of sC5b-9, C3, C4, C1-INH, and CH50, which are indicators of complement system activation and regulatory processes, in pregnant women with and without fetal growth restriction (FGR). Methods: This study enrolled eighty-six women with gestational age between 24 and 36 weeks. Maternal blood samples were obtained from 43 patients diagnosed with FGR and 43 from healthy pregnancies. Serum complement levels were measured using commercially available ELISA kits according to the manufacturer’s instructions (SunRed, China). Results: When the levels of complement activation biomarkers of pregnancies with FGR were compared with those of healthy pregnancies, the C1est level was significantly higher, C4 and CH50 levels were slightly lower, and Sc5b9 and C3 levels were similar. Conclusion: While the exact role of complement activation in FGR remains fully elucidated, the elevated levels of C1-INH in women with FGR suggest a compensatory mechanism to mitigate thrombus formation and inflammation. This adaptive response may be a potential therapeutic target for improving placental function and pregnancy outcomes.

Transforming Waste into Wealth: Advanced Carbon-Based Electrodes Derived from Refinery and Coal By-Products for Next-Generation Energy Storage.

This comprehensive review addresses the need for sustainable and efficient energy storage technologies against escalating global energy demand and environmental concerns. It explores the innovative utilization of waste materials from oil refineries and coal processing industries as precursors for carbon-based electrodes in next-generation energy storage systems, including batteries and supercapacitors. These waste-derived carbon materials, such as semi-coke, coal gasification fine ash, coal tar pitch, petroleum coke, and petroleum vacuum residue, offer a promising alternative to conventional electrode materials. They present an optimal balance of high carbon content and enhanced electrochemical properties while promoting environmental sustainability through effectively repurposing waste materials from coal and hydrocarbon industries. This review systematically examines recent advancements in fabricating and applying waste-derived carbon-based electrodes. It delves into the methodologies for converting industrial by-products into high-quality carbon electrodes, with a particular emphasis on carbonization and activation processes tailored to enhance the electrochemical performance of the derived materials. Key findings indicate that while higher carbonization temperatures may impede the development of a porous structure, using KOH as an activating agent has proven effective in developing mesoporous structures conducive to ion transport and storage. Moreover, incorporating heteroatom doping (with elements such as sulfur, potassium, and nitrogen) has shown promise in enhancing surface interactions and facilitating the diffusion process through increased availability of active sites, thereby demonstrating the potential for improved storage capabilities. The electrochemical performance of these waste-derived carbon materials is evaluated across various configurations and electrolytes. Challenges and future directions are identified, highlighting the need for a deeper understanding of the microstructural characteristics that influence electrochemical performance and advocating for interdisciplinary research to achieve precise control over material properties. This review contributes to advancing electrode material technology and promotes environmental sustainability by repurposing industrial waste into valuable resources for energy storage. It underscores the potential of waste-derived carbon materials in sustainably meeting global energy storage demands.

Molecular dynamics study of surface alkalization reaction in high calcium systems

Alkali-activated materials (AAMs) offer significant benefits in the field of civil engineering, thanks to their energy-efficient and environmentally-friendly properties, as well as their exceptional strength and durability. However, the fundamental chemical reaction underlying the use of AAMs has not yet been fully understood. The process of the silicate depolymerization of the supplementary gelling materials is determined by their nano characteristics, which have certain restrictions by using experimental techniques. In this study, we utilized reactive molecular dynamics (MD) simulations to elucidate the chemical events occurring during alkali-activation in different AAMs. The sodium hydroxide (NaOH) solution selectively dissolves the silicon chains, while the aluminum chains remain intact. Furthermore, the laminar structures of silicon and aluminum in metakaolin (MK) crystal are entirely disturbed. However, the disintegration of silicon chains is negligible, and the Slag minerals maintain their layered structure. Calcium ions are crucial in stabilizing the chemical process of alkali activation. Furthermore, this study evaluates the fluctuations in their activity. Gaining insight into the minute details of this reaction provides essential theoretical foundations for developing eco-friendly and high-performing alkali-activated concrete materials.

Modelling the Impact of NETosis During the Initial Stage of Systemic Lupus Erythematosus

The development of autoimmune diseases often takes years before clinical symptoms become detectable. We propose a mathematical model for the immune response during the initial stage of Systemic Lupus Erythematosus which models the process of aberrant apoptosis and activation of macrophages and neutrophils. NETosis is a type of cell death characterised by the release of neutrophil extracellular traps, or NETs, containing material from the neutrophil’s nucleus, in response to a pathogenic stimulus. This process is hypothesised to contribute to the development of autoimmunogenicity in SLE. The aim of this work is to study how NETosis contributes to the establishment of persistent autoantigen production by analysing the steady states and the asymptotic dynamics of the model by numerical experiment.

Особливості онтогенезу бацил впродовж розвитку від спори до вегетативної клітини

In the review, on the example of aerobic spore-forming bacteria, the problems of the development and ontogenesis of the bacterial cell are considered along with the possibilities of influencing the course of these processes. The characteristics of the main concepts "growth", "differentiation", and "development" as independent processes with their dynamic interrelation are presented. Attention is focused on the analysis of literature data on the peculiarities of vegetative cell development, starting from a spore in a dormant state and finishing with vegetative form formation. In particular, the mechanisms that maintain the spore dormant state and subsequent processes of activation, initiation, outgrowth, and vegetative cell formation are described. There are emphasized certain problems with research on the ontogenesis of bacterial cells due to the deficiency of appropriate methods, as well as the lack of a single opinion regarding individual stages of the development and vegetative form formation. It was concluded that the study of individual stages of the development of prokaryotes, which differ in spore-forming and non-spore-forming microorganisms, is still relevant. Knowledge of these processes will help scientists to develop mechanisms of influence on the ontogenesis of microorganisms.

DISCUSSION OF THE MECHANISM OF THE ELECTRICAL CONDUCTIVITY OF PURE WATER IN THE FRAMEWORK OF THE BJERRUM MODEL

An alternative mechanism of electrical conductivity and ionization of molecules in pure water is considered. Calculation of the temperature dependence for the activation energy of ionization of water molecules was carried out using data on the value of its ionic product. The calculated activation energies for the ionization and flow processes show the presence of a certain proportionality between them. This suggests that the ionization of water is caused by intermolecular forces rather than intramolecular forces. Accordingly, the electrical conductivity of water is associated with the appearance and movement in it of L and D defects of hydrogen bonds between water molecules, which have significant electrical pseudo charges and are considered in the Bjerrum model for ice. This work proposes a new interpretation of the mechanism of ionization (pseudoionization) of molecules and generation of L and D defects in water. Rotation is considered not for one, but for two of its molecules in opposite directions with partial compensation of their angular momentum, and the breaking of not three bonds for one molecule, but four bonds with neighbors for two molecules. Moreover, these four neighbors do not include molecules from water clusters that have stronger bonds, since neighboring molecules with weaker bonds can be found for the process of rotation activation. Accordingly, the exponential contribution made by molecules from water clusters is absent or small in the ionization activation energy. In this way, the activation energy for the flow, which occurs throughout the entire volume of the liquid and automatically includes molecules from clusters, differs from the activation energy of electrical conductivity, which occurs for individual molecules in chains of bonds. The presence of a maximum in the ionic product of water near 250 ⁰C can be explained by the rapid decrease in the lifetime of L and D defects with heating, which prevents the use of the standard equation for accurate calculation of the ionization activation energy above 100...200 ⁰C. However, the presence of this maximum contradicts the generally accepted model of proton hopping between neighboring hydronium and water molecules in the mechanism of its electrical conductivity.

Impact of Combined Electrolysis and Activated Sludge Process on Municipal Wastewater Treatment

Electrochemical methods for the treatment of municipal and industrial wastewater are used either independently or in conjunction with biological methods for pretreatment or posttreatment of biologically treated wastewater. In our work, the combination of these processes was studied, where pre-electrolysis was used to produce dissolved iron before the activation process. Electrolysis was also directly introduced into the activation using either iron or carbon electrodes. The surface of one iron electrode was 32.2 cm2, voltage at the electrodes was 21 V, and current was 270 mA. The surface of one carbon electrode was 7.54 cm2, current was 82.5 mA, and voltage at the electrodes was 21 V. Laboratory research on synthetic municipal wastewater treatment using a combination of electrolysis and activation processes showed that the use of iron electrodes increases the efficiency of phosphorus removal compared to its precipitation with iron salts. Electrolysis has shown a positive effect on the sedimentation properties of sludge and the destruction of filamentous microorganisms. Even though it negatively affected the respiration rates of activated sludge and the denitrification efficiency, it did not have a negative impact on the nitrification activity of sludge.

Mixed biomass-derived multi-heteroatom doped carbon-decorated Mn3O4 for a high-performance asymmetric all solid-state supercapacitor

Recently, the development of non-conventional electrochemical energy storage technologies has attracted great attention. Herein, in accordance with green strategies for the producing renewable energy storage systems, eco-friendly electrode was successfully produced from mixed biomass precursors through carbonization and activation processes. Obtained electrode (MB-AC) as a negative and its composite (Mn3O4@MB-AC) as positive electrodes were exhibited excellent electrochemical performance with high specific capacitance of 716.49 Fg−1 at 0.75 Ag−1 and 848.21 Fg−1 at 1.0 Ag−1 respectively, in 3 M KOH electrolyte. Further, for the practical application, flexible asymmetric all-solid-state supercapacitor was made. Which offer high specific capacitance of 266.46 Fg−1 at 2 Ag−1, high energy density of 119.91 Wh kg−1 at a high-power density of 1800.08 W kg−1 within a voltage window of 1.8 V. These prominent electrochemical performances suggest that selected waste biomass materials derived carbon have considerable applications in the field of energy storage technologies.

Trap states and carrier diffusion lengths in NiO/β-Ga2O3 heterojunctions

We report the electrical properties, deep trap spectra, and diffusion lengths of non-equilibrium carriers in Ni Schottky diodes and NiO/Ga2O3 heterojunctions (HJs) prepared on the same n−/n+ β-Ga2O3 epi structures. The heterojunctions decrease the reverse current of Ga2O3 high-power rectifiers. In HJs, in contrast to Schottky diodes, the capacitance and AC conductance show a prominent frequency and temperature dependence, suggesting the presence of two temperature activation processes with activation energies of 0.17 and 0.1 eV. The deep trap spectra of the Schottky diodes and HJs differ by the absence in the HJ of deep electron traps E2* with level near Ec − 0.7 eV considered to be an important center of non-radiative recombination. This correlates with the observed increase in the diffusion length of non-equilibrium charge carriers in the HJs to 370 nm compared to 240 nm in the Schottky diodes. The diffusion length of charge carriers in p-NiO was found to be quite short, 30 nm. Possible reasons for the observed differences and possible origin of the minority-trap-like feature commonly reported to be present in the deep level spectra of HJs and also observed in our experiments are discussed.

Tuning NaCo(II) Bimetallic Cooperativity to Perform Co-H Exchange / C-F Bond Activation Processes in Polyfluoroarenes.

Recent advances in cooperative chemistry have shown the potential of heterobimetallic complexes combining an alkali-metal with an earth abundant divalent transition metal for the functionalisation of synthetically relevant aromatic molecules via deprotonative metalation. Pairing sodium with cobalt (II), here we provide an overview of the reactivity of bimetallic [NaCo(HMDS)3] [HMDS = N(SiMe3)2] towards C-H and C-F functionalisation of a wide range of perfluorinated molecules. These studies also uncover the enormous potential of this heterobimetallic base to perform Co-H exchanges with excellent selectivity and exceptional stoichiometric control as well as shedding light on the key role played by the alkali-metal.

Enhancing the supercapacitive performance of a carbon-based electrode through a balanced strategy for porous structure, graphitization degree and N,B co-doping

Regarding carbon-based electrodes, simultaneously establishing a well-defined meso-porous architecture, introducing abundant hetero-atoms and improving the graphitization degree can effectively enhance their capacitive performance. However, it remains a significant challenge to achieve a good balance between defects and graphitization degree. In this study, the porous structure and composition of carbon materials are co-optimised through a ‘dual-function’ strategy. Briefly, K3Fe(C2O4)3 and H3BO3 were hybridised with a gelatin aqueous solution to form a homogeneous composite hydrogel, followed by lyophilisation and carbonisation. Owing to the dual functionality of raw materials, the graphitization, activation and hetero-atom doping processes can occur simultaneously during a one-step high-temperature treatment. The resultant carbon material exhibits a high graphitization degree (ID/IG = 0.9 ± 0.1), high hetero-atom content (N: 9.0 ± 0.3 at.%, B: 6.9 ± 0.5 at.%) and a large specific area (1754 ± 58 m2/g). The as-prepared electrode demonstrates a superior capacitance of 383 ± 1F g−1 at 1 A/g. Interestingly, the cyclic voltammetry (CV) curves exhibit a distinctive pair of broad redox peaks, which is uncommon in KOH electrolyte. Experiment data and density functional theory (DFT) simulation verify that N-5, B co-doping enhances the activity of the faradic reaction of carbon electrodes in KOH electrolyte. Furthermore, the fabricated Zn-ion hybrid supercapacitor (ZHSC) based on this carbon electrode delivers a high-energy density of 140.7 W h kg−1 at a power density of 840 W kg−1.

PH-modulated oxidation of organic pollutants for water decontamination: A deep insight into reactivity and oxidation pathway

Solution pH is one of the primary factors affecting the efficiency of water decontamination. Although the influence of pH on oxidants activation, catalyst activity, and reactive oxygen species have been widely explored, there is still a scarcity of systemic studies on the changes in the oxidation behavior of organic pollutants at different pH levels. Herein, we report the influence laws of pH on the forms, reactivities, active sites, degradation pathways, and products toxicities of organic pollutants. Changes in pH cause the protonation or deprotonation of organic pollutants and further affect their forms and chemistry (e.g., electrostatic force, hydrophobicity, and oxidation potential). The oxidation potential of organic pollutants follows the order: protonated form > pristine form > deprotonated form. Moreover, protonation or deprotonation can modify the active sites and degradation pathways of organic pollutants, wherein deprotonation renders them more susceptible to electrophilic attack, while protonation reduces their activity against electrophilic and nucleophilic attacks. Additionally, pH adjustments can modify the degradation pathway and the toxicity of transformation products. Overall, pH changes can affect the oxidation fate of organic pollutants by altering their structure, which distinguishes it from the effect of pH on oxidants or oxidant activation processes.

A new method for tracking the preparatory activation of target templates for visual search with high temporal precision.

Efficiently selecting task-relevant objects during visual search depends on foreknowledge of their defining characteristics, which are represented within attentional templates. These templates bias attentional processing toward template-matching sensory signals and are assumed to become anticipatorily activated prior to search display onset. However, a direct neural signal for such preparatory template activation processes has so far remained elusive. Here, we introduce a new high-definition rapid serial probe presentation paradigm (RSPP-HD), which facilitates high temporal resolution tracking of target template activation processes in real time via monitoring of the N2pc component. In the RSPP-HD procedure, task-irrelevant probe displays are presented in rapid succession throughout the period between task-relevant search displays. The probe and search displays are homologously formed by lateralized "clouds" of colored dots, yielding probes that occur at task-relevant locations without confounding template-guided and salience-driven attentional shifts. Target color probes appearing at times when a corresponding target template is active should attract attention, thereby eliciting an N2pc. In a condition where new probe displays appeared every 50 ms, probe N2pcs were reliably elicited during the final 800 ms prior to search display onset, increasing in amplitude toward the end of this preparation period. Analogous temporal profiles were also observed with longer intervals between probes. These findings show that search template activation processes are transient and that their temporal profile can be reliably monitored at high-sampling frequencies with the RSPP-HD paradigm. This procedure offers a new route to approach various questions regarding the content and temporal dynamics of attentional control processes.

Nitrogen-phosphorus dual-doped auricularia auricula porous carbon as host for Li-S battery.

A nitrogen-phosphorus dual-doped porous spore carbon (NP-PSC) positive electrode matrix was prepared using native auricularia auricula as solid medium based on the principle of biomass rot. Yeast was introduce and cultured by the auricularia auricula solid medium. The freeze-drying and carbonization activation processes made the materials present a three-dimensional porous spore carbon aerogel properties. Yeast fermentation transformed auricularia auricula from blocky structure to porous structure and introduced nitrogen-phosphorus dual-doping. The physical and chemical properties of the prepared materials were characterized in detail. Electrochemical performance of NP-PSC in Li-S batteries was systematically investigated. Porous structure and heteroatom-doping improved the electrochemical performance, which is much superior to conventional activated carbon materials.

SARS-CoV-2 infection activates inflammatory macrophages in vascular immune organoids

SARS-CoV-2 provokes devastating tissue damage by cytokine release syndrome and leads to multi-organ failure. Modeling the process of immune cell activation and subsequent tissue damage is a significant task. Organoids from human tissues advanced our understanding of SARS-CoV-2 infection mechanisms though, they are missing crucial components: immune cells and endothelial cells. This study aims to generate organoids with these components. We established vascular immune organoids from human pluripotent stem cells and examined the effect of SARS-CoV-2 infection. We demonstrated that infections activated inflammatory macrophages. Notably, the upregulation of interferon signaling supports macrophages’ role in cytokine release syndrome. We propose vascular immune organoids are a useful platform to model and discover factors that ameliorate SARS-CoV-2-mediated cytokine release syndrome.