Spherical Structure Research Articles

Effect of Hydroxyapatite Nanowires on Formation and Bioactivity of Osteoblastic Cell Spheroid.

Compared with traditional high-density cell spheroids, which are more prone to core necrosis, nanowires effectively improve the biological activity of core cells in spheroids, emanating more innovations for optimizing the internal cell survival environment and providing differentiation signals. In this study, hydroxyapatite nanowires (HAW), which provide numerous material exchange channels for internal cells by interpenetrating into cell spheroids, were added to osteoblast precursor (MC3T3-E1) cell spheroids. HAW, synthesized using the hydrothermal method, was used as a regulatory material to prepare uniformly sized 3D composite spheroids with good biological activity. Subsequently, material characterization and biocompatibility tests were performed on HAW, and the biological activity and osteogenic differentiation ability of the cell spheroids were tested. Notably, in 2D coculture, HAW displayed a certain attraction to MC3T3-E1 cells and promoted cell aggregation toward it. The content of HAW determined whether composite cell spheroids can form aggregated spherical structures, and incorporation of HAW alleviated core necrosis and enhanced the osteogenic phenotype. In summary, these findings indicate that the prepared HAW-bone cell composite spheroids can potentially be used as building blocks for the construction of large high-density biomimetic tissues and organoids using 3D bioprinting technology.

Mitochondria-giant lipid droplet proximity and autophagy suppression in nitrogen-depleted oleaginous yeast Lipomyces starkeyi cells.

Balancing energy production and storage is a fundamental process critical for cellular homeostasis in most eukaryotes that relies on the intimate interplay between mitochondria and lipid droplets. In the oleaginous yeast Lipomyces starkeyi under nitrogen starvation, lipid droplet forms a single giant spherical structure that is easily visible under a light microscope. Currently, how mitochondria behave in L. starkeyi cells undergoing giant lipid droplet formation remains unknown. Here we show that mitochondria transition from fragments to elongated tubules and sheet-like structures that are in close proximity to a giant lipid droplet in nitrogen-depleted L. starkeyi cells. Under the same conditions, mitochondrial degradation and autophagy are strongly suppressed, suggesting that these catabolic events are not required for giant lipid droplet formation. Conversely, carbon-depleted cells suppress mitochondrial elongation and lipid droplet expansion, whereas they promote mitochondrial degradation and autophagy. We propose a potential link of mitochondrial proximity and autophagic suppression to giant lipid droplet formation.

Transcriptomic atlas of the morphologic development of the fungal pathogen Coccidioides reveals key phase-enriched transcripts.

Coccidioides spp . are highly understudied but significant dimorphic fungal pathogens that can infect both immunocompetent and immunocompromised people. In the environment, they grow as multicellular filaments (hyphae) that produce vegetative spores called arthroconidia. Upon inhalation by mammals, arthroconidia undergo a process called spherulation. They enlarge and undergo numerous nuclear divisions to form a spherical structure, and then internally segment until the spherule is filled with multiple cells called endospores. Mature spherules rupture and release endospores, each of which can form another spherule, in a process thought to facilitate dissemination. Spherulation is unique to Coccidioides and its molecular determinants remain largely unknown. Here, we report the first high-density transcriptomic analyses of Coccidioides development, defining morphology-dependent transcripts and those whose expression is regulated by Ryp1, a major regulator required for spherulation and virulence. Of approximately 9000 predicted transcripts, we discovered 273 transcripts with consistent spherule-associated expression, 82 of which are RYP1 -dependent, a set likely to be critical for Coccidioides virulence. ChIP-Seq revealed 2 distinct regulons of Ryp1, one shared between hyphae and spherules and the other unique to spherules. Spherulation regulation was elaborate, with the majority of 227 predicted transcription factors in Coccidioides displaying spherule-enriched expression. We identified provocative targets, including 20 transcripts whose expression is endospore-enriched and 14 putative secreted effectors whose expression is spherule-enriched, of which 6 are secreted proteases. To highlight the utility of these data, we selected a cluster of RYP1 -dependent, arthroconidia-associated transcripts and found that they play a role in arthroconidia cell wall biology, demonstrating the power of this resource in illuminating Coccidioides biology and virulence.

In Situ Electrochemical Conversion of Biomass-Derived 5-Hydroxymethylfurfural into 2,5-Furandicarboxylic Acid by Time-Controlled Aerosol-Assisted Chemical Vapor Deposited FeNi Catalyst.

The conversion of 5-hydroxymethylfurfural (HMF) into valuable chemicals, such as 2,5-furandicarboxylic acid (FDCA), is pivotal for sustainable chemical production, offering a renewable pathway to biodegradable plastics and high-value organic compounds. This pioneering study explores the synthesis of FeNi nanostructures via aerosol-assisted chemical vapor deposition (AACVD) for the electrochemical oxidation of HMF to FDCA. By adjusting the deposition time, we developed two distinct nanostructures: FeNi-40, which features nanowires with spherical terminations, and FeNi-80, which features aggregated spherical structures. X-ray diffraction (XRD) confirmed that both nanostructures possess a phase-pure face-centered cubic (FCC) crystal structure. Electrochemical tests conducted using FeNi nanocatalysts on Ni foam revealed that FeNi-40 requires a significantly lower onset potential for HMF oxidation (1.32 V vs RHE) compared to FeNi-80 (1.40 V vs RHE). This difference is attributed to the unique nanowire morphology of FeNi-40, which provides a higher density of active sites and a larger electrochemically active surface area, thereby enhancing the efficiency of the electrochemical process. When tested in an H-type electrolyzer with a Nafion membrane, FeNi-40 demonstrated a remarkable Faradaic efficiency of 96.42% and a high product yield, underscoring the potential of morphology-controlled FeNi nanostructures to enhance the efficiency of sustainable electrochemical processes significantly.

Preparation of fly ash zeolite supported ZnO/Co3O4 catalyst for the photocatalytic degradation of xanthate under visible light

The development of high-value utilization technology of fly ash plays an important role in promoting environmental protection and social and economic development. In this paper, a novel composite photocatalyst Z-ZnO/Co3O4 is synthesized by loading ZnO/Co3O4 on the surface of fly ash zeolite. In addition, the properties of Z-ZnO/Co3O4 are characterized by variety of methods. The results show that the surface of cubic A-type zeolite is coated with ZnO/Co3O4 composite, forming an open spherical flower-like structure with a typical p-n heterostructure, which plays a positive role in reducing the band gap and the recombination rate of photogenerated electrons and holes of the composite catalyst, thus improving the degradation efficiency of xanthate. The degradation rate toward xanthate of Z-ZnO/Co3O4 is 97.62 % after simulated sunlight irradiation for 120 min under the optimum conditions, which is higher than that of Z-ZnO and Z-Co3O4, respectively. Meanwhile, the experimental results indicate that h+ plays a leading role in the catalytic reaction system. Furthermore, degradation rate toward xanthate of Z-ZnO/Co3O4 decreases slightly from 97.62 % to 88.24 % after five cycles, indicating its remarkable durability and stability.

Single-Atom Doped Fullerene (MN4-C54) as Bifunctional Catalysts for the Oxygen Reduction and Oxygen Evolution Reactions.

Development of high-performance oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) catalysts is crucial to realizing the electrolytic water cycle. C60 is an ideal substrate material for single atom catalysts (SACs) due to its unique electron-withdrawing properties and spherical structure. In this work, we screened for a novel single-atom catalyst based on C60, which anchored transition metal atoms in the C60 molecule by coordination with N atoms. Through first-principles calculations, we evaluated the stability and activity of MN4-C54 (M = Fe, Co, Ni, Cu, Rh, Ru, Pd, Ag, Pt, Ir, Au). The results indicate that CuN4-C54, which is based only on earth-abundant elements, exhibited low overpotentials of 0.46 and 0.47 V for the OER and ORR, respectively, and was considered a promising bifunctional catalyst, showing better performance than the noble-metal ones. In addition, according to the linear relationship of intermediates, we established volcano plots to describe the activity trends of the OER and ORR on MN4-C54. Finally, d-band center and crystal orbital Hamiltonian populations methods were used to explain the catalytic origin. Suitable d-band centers lead to moderate adsorption strength, further leading to good catalytic performances.

Evaluation of Processing Parameters in the Solvothermal Synthesis of Cu-Rich Tetrahedrites for Potential Application as Thermoelectric Materials

The major issue associated with thermoelectric performance is the low efficiency of power conversion. The main challenge is achieving a combination of high Seebeck coefficient, high electrical conductivity, and low thermal conductivity for a significantly improved figure of merit (ZT). Developing strategies include the production of tetrahedrites with an intrinsically low thermal conductivity through the solvothermal method, using a low reaction time and processing temperature. Here, we report on the preparation of Cu-rich tetrahedrites through the solvothermal technique at low temperature, providing a promising strategy for the preparation of materials with potential applications in thermoelectricity. The influence of synthesis reaction time and temperature on the morphological, structural, and thermoelectrical properties of the samples was investigated through different characterization techniques. Tetrahedrite synthesized at 180 °C for 19 h yielded a favorable ZT value of >0.43 and a thermal conductivity of 0.2 Wm−1 K−1 (423 K), related to the Sb3+/Sb5+ and Cu+/Cu2+ ratio, as was observed by XPS. The cubic tetrahedrite phase attributed to the (222) plane was confirmed by XRD and TEM and the intense Raman mode observed at 351 cm−1. SEM images revealed that nanotetrahedral Cu-rich tetrahedrites efficiently assemble into spherical structures, resulting in an improvement in the Seebeck coefficient (437 µVK−1) and electrical conductivity.

A method for optimizing different geometric shields of D-T neutron generators by combining BP neural network and Analytic Hierarchy Process

In this paper, an optimization of shielding structures with different geometries is established for the D-T neutron generator system by combining Back Propagation (BP) neural network and Analytic Hierarchy Process (AHP). The D-T neutron generator (Model NG-9) used in the system was developed independently by Northeast Normal University. After investigating the rule of shielding performance among spherical, cylindrical and cubic geometries, the spherical shield is selected for BP neural network prediction to determine the total dose rate through it. Information about spherical multilayer-shielding structures and properties calculated by MCNP code is used to train the neural network. The predicted result serves as a parameter of the evaluation function, which provides a comprehensive assessment of the dose rate penetrated the shield, the shielding mass, and the shielding volume. Together with AHP, the weight factors are determined for all the optimization objectives to construct the evaluation function. By comparing its values, the optimal shielding structures for spherical, cylindrical and cubic materials are found. Against MCNP simulated values, the total dose rates’ errors of the optimal shielding structures for the sphere, cylinder, and cube are 1.72 %, -4.94 %, and -5.17 %, respectively. This result demonstrates that the combination of BP neural network and AHP is more effective in addressing multi-objective optimization problems related to the design of radiation shielding for various geometries.

A versatile opened hollow carbon sphere with highly loaded antimony alloy for ultra-stable potassium-ion storage

Carbon materials meet the stringent practical requirements for anodes for potassium-ion batteries (PIBs) due to their abundance and chemical stability. The major issue of carbon-based anodes is the low specific capacity and poor cyclic stability. Equally importantly, scalable synthesis approaches for electrodes are highly desired for the future application in large-scale energy storage systems. Herein, we developed a novel composite of Sb encapsulated in N/P co-doped opened hollow carbon spheres (N/POHCs) with high Sb loading through a simple carbonization and subsequent impregnation process. Beneficial from the virtue of abundant pyridinic-N−P bonding and opened hollow spherical structure advantages, N/POHCs exhibit much lower diffusion barrier than that of pure carbon, prominent Sb carrier capability, as well as the extraordinary resistance to volume expansion. The resulting Sb@N/POHCs composite delivers a high specific capacity of 533.3 mAh g−1 at 0.1 A g−1 with an initial Coulombic efficiency of 83 %, and can maintain a specific capacity of 345 mAh g−1 at 1 A g−1 after 4000 cycles. This work provides rational structure design with universal carrier capability of active materials to achieve high-capacity and long cycle life anode for advanced PIBs accompanied by the potential for large-scale production.

Application of precursor with ultra-small particle size and uniform particle distribution for ultra-high nickel single-crystal cathode materials by coprecipitation method

Ultra-high nickel single-crystal cathode materials have become the most promising for lithium-ion batteries. However, the preparation of ultra-high nickel single-crystal precursors by a continuous coprecipitation method has the disadvantages of large particle size, wide distribution, poor morphology. The extent of the inhomogeneous reactions can be more severe in single-crystal cathodes with larger particle size. Herein, the coprecipitation method with a solid concentrator was adopted, and citrate sodium was used as a complexing agent to improve the physical properties of precursors and electrochemical performance of single-crystal cathode materials. By analyzing the morphology and agglomeration mechanism of the precursor nucleuses under different pH values, it was found that hexagonal nanosheets grew along the 101 direction, and the primary particles showed thicker at pH of 11.4. The hexagonal nanosheets grew along the 001 direction, and the primary particles showed finer at pH of 12.2. The morphology and particle size uniformity of the secondary particles formed by agglomeration at these two pH values showed poor. However, hexagonal nanosheets grew synergistically along the 001 and 101 directions at pH of 11.8, so the primary particles with uniform particle size gradually agglomerated, and then the secondary particles with ultra-small particle size and uniform distribution obtained. Compared to materials prepared by the traditional continuous coprecipitation method, the precursor displays a smaller particle size(D50 = 1.8 µm), higher sphericity, uniformity and denser internal structure. In order to evaluate the performance of Ni0.94Co0.04Mn0.02(OH)2 with ultra-small particle size, the sintering conditions of LiNi0.94Co0.04Mn0.02O2 need to be explored. It was found that the LiNi0.94Co0.04Mn0.02O2 cathode material prepared at 790 °C exhibited higher discharge capacity, cycle and rate performance, compared to materials prepared at 760 °C and 820 °C. We further utilized TEM, EPMA, and XPS to test the internal structure and valence state of LiNi0.94Co0.04Mn0.02O2 cathode material. The results show that the LiNi0.94Co0.04Mn0.02O2 calcined at 790 °C has a good single crystal structure. The LiNi0.94Co0.04Mn0.02O2 cathode materials inherited the structure and particle size of Ni0.94Co0.04Mn0.02(OH)2 precursors, and displayed discharge capacity of 194.7 mAh/g and capacity retention rate of 89.8 % after 100 cycles at 1 C. The microstructure and phase transition of the as-prepared cathode material are well-maintained after long-term cycling, without obvious inter-crystalline micro-crack. The results indicate that its electrochemical performance is better than that of cathode materials with precursors prepared by a continuous coprecipitation method. This work provides new insights for the preparation of small-particle-size precursor and single-crystal cathode materials.

Study on photocatalytic degradation and antibacterial properties of conjugated microporous polymers/TiO2 composite membranes

Conjugated microporous polymers (CMPs) are widely used in the field of photocatalysis due to their unique conjugated structures and various synthesis methods. Herein, we report the design and synthesis of conjugated microporous polymers hollow spheres (CMPs-HS) superhydrophilic modified by acetylcysteine (CMPs-HS-S) and compounded with the inorganic semiconductor material titanium dioxide (CMPs-HS-S/TiO2) for efficient photocatalytic degradation. To facilitate recycling, the composite membrane material was prepared by combining the materials mentioned above with PVDF membrane. The composite membrane materials had good hydrophilic and photocatalytic properties. Under visible light, the degradation rate of tetracycline (TC) (10 mg/L 180 min) reached 90 %, and the bactericidal rates for Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were 89 % and 99.99 %, respectively. The efficient photocatalytic performance of the composite membranes could be attributed to the hollow sphere structure of CMPs and the role of TiO2 as a photogenic electron transfer platform. Additionally, the hydrophilicity of the membrane also helped to accelerate the occurrence of photocatalytic reactions. After electron paramagnetic resonance (EPR) detection, h+, 1O2 and O2− were proved to be important reactive substances, which played a major role in degradation. These studies reflect the versatility of CMPs-based photocatalysts and provide a new idea for the future development of CMPs-based photocatalysts.

Wrinkled Shrinkage on Surface Monophasic Structure of Floating Refractory Alloy Droplets Solidified in Space Environment

AbstractThe surface‐wrinkled shrinkage structure of spheres is very common and also quite intriguing to explore and reveal the analogous droplet solidification kinetics in the space environment. Here, a liquid‐to‐solid phase transition experiment of floating refractory alloy droplets is designed to study the surface wrinkled shrinkage structures aboard China Space Station with a 10−5 gravity level. The experimental Ti‐Ni‐V alloy droplets undergo an extremely high overheating temperature beyond 1800 K and then achieve a supercooling of 307 K, displaying a strong thermodynamic metastability. The spherical surface deformation structures of this alloy under microgravity coupled with extreme metastable solidification are explored. Moreover, through the active control of metastable rapid solidification, a surface monophasic structure and a B2 structure capable of stress‐induced martensitic transformation are facilitated by wrinkled shrinkage dynamics under microgravity. Their findings shed further light on the surface deformation structures during the microgravity solidification process.

The growth mechanism and optical properties of flower-like porous Gd2O2S:Er3+/Yb3+ phosphor

The self-assembly mechanism of porous materials has always been a hot topic and a challenging issue in research. What factors induce the self-assembly process, and how is the temperature sensing performance related to it? Innovatively, in this paper, Gd2O2S:Er3+/Yb3+ phosphors with different morphologies were synthesized, and elucidated the formation mechanism of flower-like structures through relevant theorems, formulas, and experiments, proposing that polar molecules and dipole-dipole interactions guide the synergistic effect of van der Waals forces and hydrogen bonding, which ultimately induces the self-assembly of spherical structures into flower-like ones. In addition, four representative intermediates were selected to investigate their luminescence and temperature sensing properties. The results show that the flower-like sample can respond more effectively to changes in ambient temperature because of its rich pore structures, and thus exhibit better temperature sensing performance. In-depth research on the self-assembly mechanism of materials helps to predict and regulate their properties, and the unique characteristics of flower-like sample provide new ideas for material selection in the field of high-precision temperature measurement.

The impact of heat treatment process on the drilling characteristics of Al–5Si–1Cu–Mg alloy produced by sand casting

Aluminum–Silicon (Al–Si) based materials are commonly preferred in engineering studies requiring high mechanical performance as an alternative to steel materials. These alloys are especially preferred in the automotive industry, aerospace components and heavy machinery parts. In post-casting processes, machining operations are of great importance for high geometric precision, surface quality and longer fatigue life in mechanical environments. In this research, the microstructural, mechanical and machining characteristics of the Al–5Si–1Cu–Mg material produced by sand casting method in both as-cast (AC) and heat-treated (HTed) (Solid solution, quenching and aging-SQA) states were experimentally investigated. Microstructural examinations were carried out with optical microscope and SEM images. Mechanical properties were determined by tensile and hardness tests. Then, drilling experiments were performed in the CNC vertical machining center with 8 mm diameter uncoated HSS (High Speed Steel) cutting tools at constant cutting conditions (i.e., cutting speed-V: 125 m/min, feed rate-f: 0.05 mm/rev and depth of cut-DoC: 15 mm). In microstructural investigations, it was determined that the microstructure of the Al–5Si–1Cu–Mg material in AC state consists of α-Al, eutectic Si, β-Fe (β-Al5FeSi) and π-Fe (π-Al8Mg3FeSi6) intermetallics. After the SQA, the existing phases generally exhibited a spherical structure, and it was seen that the β phase in the microstructure transformed into the Ɵ (Al7FeCu2) phase. SQA improved the hardness, yield and tensile durability of the material, whereas decreasing the elongation to fracture. SQA process improved the machining characteristics of the material by decreasing thrust force, moment, surface roughness and built-up edge (BUE) formation. The machined subsurface structure of HTed alloy under constant cutting conditions was determined to be more stable and smooth and the machined surface microhardness of HTed alloy was higher compared to as-cast alloy due to the effect of solid precipitation hardening. In addition, shorter and more broken chips occurred in the machining of HTed alloys due to the effect of low elongation to fracture.

Development of oral pH-sensitive redox nanotherapeutics for gastric ulcer therapy

Gastric ulcer is a common gastrointestinal disorder worldwide. Although its pathogenesis is unclear, the overproduction of reactive oxygen species (ROS), which results in an oxidative imbalance, has been reported as a central driving mechanism. Within the scope of this investigation, we developed two different self-assembling redox nanoparticles (RNPs) with ROS-scavenging features for the oral treatment of gastric ulcers. One of them, referred to as RNPN, disintegrates in response to acidic pH, whereas the other, denoted as RNPO, remains intact regardless of pH variations. Both types of RNPs showed different free radical scavenging activities in vitro. Protonation of the amino linkages in the side chains of RNPN caused the micelle structure to collapse and the nitroxide radicals encapsulated in the core were exposed to the outside, resulting in a significant increase in antioxidant capacity as the pH decreases. In contrast, RNPO maintained its spherical structure and consistent antioxidant reactivity irrespective of pH changes. The in vivo gastric retention of orally administered RNPN was significantly improved compared to that of RNPO which might be explained by the increased exposure of cationic protonating segments in RNPN on the negatively charged gastric mucosal surface. Owing to its improved gastric retention and enhanced ROS scavenging capacity under acidic pH conditions, RNPN exhibited superior protective effects against oxidative stress induced by aspirin in a gastric ulcer mouse model compared to RNPO. In addition, neither RNPN nor RNPO resulted in severe lethal effects or significant changes in the morphology of zebrafish embryos, indicating their biosafety. Our results suggest that the oral administration of RNPs has a high therapeutic potential for gastric ulcer treatment.

The mouse Balbiani body regulates primary oocyte quiescence via RNA storage

In mammalian females, the transition from dormancy in primordial follicles to follicular development is critical for maintaining ovarian function and reproductive longevity. In mice, the quiescent primary oocyte of the primordial follicle contains a Balbiani body (B-body), an organelle aggregate comprised of a spherical structure of Golgi complexes. Here we show that the structure of the B-body is maintained by microtubules and actin. The B-body stores mRNA-capping enzyme and 597 mRNAs associated with mRNA-decapping enzyme 1 A (DCP1A). Gene ontology analysis results indicate that proteins encoded by these mRNAs function in enzyme binding, cellular component organization and packing of telomere ends. Pharmacological depolymerization of microtubules or actin led to B-body disassociation and nascent protein synthesis around the dissociated B-bodies within three hours. An increased number of activated developing follicles were observed in ovaries with prolonged culture and the in vivo mouse model. Our results indicate that the mouse B-body is involved in the activation of dormant primordial follicles likely via translation of the B-body-associated RNAs in primary oocytes.

Folate-Functionalized Chitosan-PLGA Nanoparticles: A Novel approach for targeted osthole delivery in pancreatic cancer

Efficient drug delivery systems targeting cancer cells are crucial for enhancing cancer therapy. In this study, we developed PLGA nanoparticles coated with folate-conjugated chitosan (osthole-PLGA-NPs/CS-FA) to deliver osthole to cancer cells and investigated its inhibitory and molecular signaling mechanisms in the PANC-1 pancreatic cancer cell line. Field emission scanning electron microscopy (FESEM) revealed that osthole-PLGA-NPs/CS-FA had a spherical structure with a uniform size distribution. Dynamic light scattering (DLS) analysis showed an average size of 171.76 nm, a dispersion index 0.26, and a surface charge of + 33.08 mV, indicating stability and uniform dispersion. Fourier-transform infrared (FTIR) spectrum analysis confirmed the successful incorporation of osthole into the PLGA nanoparticles, with an encapsulation efficiency of 93.12 %. These physicochemical properties suggest efficient cellular uptake and targeted delivery. The antioxidant potential of osthole-PLGA-NPs/CS-FA was evaluated using the ABTS assay, showing concentration-dependent inhibition of free radicals with an IC50 value of 172.95 μg/mL. The anticancer properties were assessed using the MTT assay, demonstrating a significant and concentration-dependent cytotoxic effect on PANC-1 cells (IC50 = 31.2 μg/mL) with minimal impact on normal human foreskin fibroblast (HFF) cells. DAPI staining and flow cytometry analyses confirmed a concentration-dependent increase in apoptosis in PANC-1 cells. The nanoparticles induced upregulation of Bax and downregulation of Bcl2, indicating activation of the intrinsic mitochondrial apoptotic pathway. The anti-angiogenic activity of osthole-PLGA-NPs/CS-FA was evaluated using the chick chorioallantoic membrane (CAM) assay. The results showed significant inhibition of angiogenesis in a concentration-dependent manner, starting at 40 μg/mL and increasing up to 120 μg/mL. In conclusion, osthole-PLGA-NPs/CS-FA nanoparticles exhibit promising potential for targeted pancreatic cancer therapy by enhancing cellular uptake, inducing apoptosis, and inhibiting angiogenesis.

Preparation of nano-TiO2 spherical catalyst doped with nonmetallic elements for potential use in CO2 reduction

Abstract P (St-HEA) microsphere was synthesized as template to prepare TiO2. Nano TiO2 spheres, nitrogen doped TiO2 (N-TiO2) spheres and sulfur doped TiO2 (S-TiO2) spheres were prepared by sol-gel method with the above template. The samples were characterized by XRD, SEM, and XPS. The results showed that TiO2 from sulfur and nitrogen atoms in thiourea and urea in situ doped in the crystal lattice. The TiO2 spherical catalyst doped with nonmetallic elements showed typical anatase phase at lower temperature, and spheres structure with pores and different particle size about 200 nm to 1μm. The obtained TiO2 spherical catalyst doped with nonmetallic elements may potentially use in the photo-catalysis of CO2 reduction.

Estimation and research of the temperature field models of large space spherical mesh shell structures under localized fire

This paper firstly investigated fire dynamics characteristics and the temperature field distributions of large space spherical mesh shell (SMS) structures under localized fire in FDS, and divided the temperature fields into plume region, smoke accumulation region and ceiling jet region. Based on the classical axisymmetric plume model, the predictive models for the steady-state and transient temperature fields in different fire regions for large space SMS structures were proposed in this paper. Thereafter, the proposed temperature models were compared with the simulated results and experimental test results by other scholars, and they were in good agreement. In order to further discover the realistic fire development progress and temperature distribution of large space fire, and validate the proposed temperature field models, this paper designed and conducted three full-scale large space fire tests (Test-1 ∼ Test-3) with different fire source powers in a large space building. Results showed that temperature fields of large space fires could be consisted of near-fire region (Flame region) and far-fire region (Plume region and Ceiling jet region). The steady-state fire source powers were tested for 443 kW, 886 kW, 1090 kW for Test-1, Test-2 and Test-3, respectively, while their maximum temperatures of the roof reached 75 °C, 105 °C and 120 °C. Based on McCaffrey plume model, we further proposed the transient temperature model in flame region for large space structures, and its accuracy was verified by the test results. Moreover, the proposed steady-state and transient temperature fields for large space SMS structures were compared with the tested temperature field data, and the tested and predicted temperature curves were generally in good agreement in plume and ceiling jet regions. Finally, the test results aimed to provide a scientific basis and reference for the fire safety and structural fire-resistant design of large space buildings.

Regulation of receptor function in NiCo2O4-SnO2 heterojunction for H2S detection at room temperature

In recent years, the World Health Organization has increasingly emphasized air quality in production environments, leading to heightened societal demands for monitoring of pollutant gases at room temperature. Traditional semiconductor gas-sensitive materials, such as tin oxide (SnO2), have their gas-sensing performance largely limited by their receptor functions, resulting in common issues like low response and poor recovery at room temperature. Spinel-type bimetallic oxides, such as nickel cobaltate (NiCo2O4), offer a unique solution due to their rich adsorption sites on the surface, which provide distinctive receptor functions for detecting toxic gases at room temperature. Herein, NiCo2O4 is synthesized via a one-step hydrothermal method, with a porous spherical cluster structure, and combined with SnO2 to form a heterojunction. The NiCo2O4-SnO2 heterojunction film gas sensor exhibits excellent gas-sensing performance for H2S at room temperature, including high response, short response time, good repeatability, and selectivity. Additionally, the unique receptor functions of the NiCo2O4 were analyzed through first-principles calculations, revealing a semiconductor p-n conversion phenomenon in the presence of H2S gas. The composite also demonstrates a conversion from p-n heterojunction to n-n homojunction during the sensing process, enhancing its gas-sensing performance. This work not only addresses the receptor function limitations of traditional gas-sensitive semiconductor but also provides a feasible approach for controlling carrier types in semiconductors.