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A milled recycled asphalt pavement (RAP) particle can be a cluster of one or more aggregates coated with an aged RAP binder. While RAP material is added to virgin aggregates and binder in a pugmill, the RAP cluster undergoes dissociation or agglomeration, depending on the cluster size and thermo-physical conditions inside the pugmill. The degree of dissociation or agglomeration of RAP material has an important relation with the degree of RAP binder availability. The RAP binder availability in mix design depends on the exposed surface area of dissociated coarse RAP particles and also on the agglomeration tendency of fine RAP particles. In the present study, the degree of RAP binder availability (DoAv), cluster dissociation of course RAP, and agglomeration tendency of fine RAP particles were examined at different mixing durations inside an asphalt pugmill—60 s, 120 s, and 180 s. The study examined whether the RAP cluster dissociation and postmixing agglomeration has any effect on the RAP binder availability. The degree of RAP binder availability of RAP mix was found by determining the virgin binder requirement of RAP mixes in excess of optimum binder content determined for the control mix prepared using virgin aggregates. Cluster dissociation and agglomeration was studied by hot mixing of RAP fractions in a pugmill with abrasive charges, followed by sieving. The statistical analysis of data found that RAP mixes incorporating fractionated fine RAP material exhibited higher DoAv at every mixing duration. For mixes incorporating fractionated coarse RAP, cluster dissociation index was positively correlated with DoAv, which implied that RAP cluster dissociation is a possible reason for RAP binder availability. In mixes incorporating fractionated fine RAP fractions, the RAP particles got agglomerated. The agglomeration index was found to correlate well with RAP binder availability, thereby establishing that agglomeration tendency in fine RAP fractions can be considered as an indicator of RAP binder availability. [ABSTRACT FROM AUTHOR]

Borophosphosilicate glasses with varying sodium ion concentrations were investigated for their, structural, thermal, and electrical properties. All the obtained glasses were transparent except the glass with the highest sodium content, which exhibited translucency due to inhomogeneities. Increasing sodium content led to reduced boron and silicon content while maintaining a constant B/Si ratio, indicating progressive depolymerization of the glass network. Confocal microscopy, scanning electron microscopy, and atomic force microscopy showed homogeneous and granular structure for samples with lower sodium content, but higher sodium content resulted in visible agglomeration/nanocrystallization. X-ray diffractograms showed amorphous nature for most samples, with samples doped with the highest concentrations of Na 2 O showing several broad reflections suggesting nanoscale crystallinity. Fourier-transform infrared spectroscopy revealed shifts in dominant bands with increasing sodium content, indicating depolymerization of the borate network. An observed decrease in glass transition temperature and thermal stability with increasing sodium content was attributed to depolymerization and formation of non-bridging oxygens. Impedance spectroscopy revealed two relaxation processes associated with the transport of Na+ ions through two different regions. DC conductivity and activation energy predominantly increased with the sodium ion content at high temperatures. [ABSTRACT FROM AUTHOR]

The composition of a pasty propellant for small-sized space engines has been proposed. For this propellant, a research of the burning process was carried out. This research included the determination of the burning rate law, the characteristics of the agglomeration process, and the properties of the surface layer. The presence of an intermediate structure, a skeleton layer, during the burning of such propellants, and the nature of the influence of pressure, additives, and the size of oxidizer particles on this structure, have been established. The determining influence of this structure on the burning process is shown. Composition solutions that provide control over the burning rate law of such propellants are determined. These solutions make it possible to change the absolute value of the burning rate, as well as its dependence on pressure. Regularities of the agglomeration process have been established. These regularities are associated with the features of the formation of the skeleton layer, which depend on the structure of the propellant, pressure, and the presence of additives. [ABSTRACT FROM AUTHOR]

[Display omitted] • 3D printing technology is used to construct a multi-layer structure inside the electrode to improve the electrochemical performance of the electrode. • The effective coordination between the material and the internal structure of the electrode improves the electrochemical performance of the electrode. • The layered structure between the asymmetric positive and negative printed electrodes promotes the transfer and transmission of charge between the electrodes. • A synthesis strategy for improving electrode performance of micro supercapacitor is proposed. The architecture of electrodes plays a pivotal role in the transfer and transportation of charges during electrochemical reactions. Selecting optimal electrode materials and devising well-conceived electrode structures can substantially enhance the electrochemical performance of devices. This manuscript leverages 3D printing technology to fabricate asymmetric supercapacitor devices featuring regular layered configurations. By investigating the impact of various materials on the internal architecture of printed electrodes, we establish a stratified electrode structure with an orderly arrangement, thereby significantly improving asymmetric charge transfer between electrodes. The application of 3D printing technology to construct electrode structures effectively mitigates the agglomeration of electrode materials. The 3D-printed VCG//MXene devices demonstrate exceptional areal capacitance (205.57 mF cm−2) and energy density (60.03 μWh cm−2), with a power density of 0.174 W cm−2. Consequently, selecting appropriate materials for fabricating printable electrode structures and achieving efficient 3D printing is anticipated to offer novel insights into the construction and enhancement of miniature asymmetric micro-supercapacitor (MSCs) devices. [ABSTRACT FROM AUTHOR]

The high-temperature roasting/smelting process of copper and zinc concentrates will cause the mercury in the concentrate to evaporate into the flue gas, and most of the mercury in the flue gas will eventually enter the waste acid in its ionic form. A highly efficient mercury removal agent M201 with long carbon chains and loaded active functional groups can adsorb and disperse fine particles for mercury removal in the system. Through bridging, the linear structure is woven into a network to achieve large-scale capture and dispersion of fine particles and colloidal substances. The recommended operating conditions for developing mercury deep purification technology are as follows: M201 reagent concentration of 50 g/L, 6 mL/L added acid solution, room temperature, mixing time of 5 min, air flotation time of 10 min, ventilation rate of 0.1 L/min, H2SO4 concentration of 33.67 g/L, and the residual mercury content of 2 mg/L (the mercury content reaches 0.01 mg/L after two-stage mercury removal treatment). Meanwhile, the residual arsenic content is 21.9 mg/L. This study shows a better separation of arsenic and mercury and achieves one-step mercury removal. [ABSTRACT FROM AUTHOR]

[Display omitted] • The PPC contains a bunch of heteroatoms to narrow the polarization of material under high current density conditions. • The presence of PPC leads to the formation of NFVP nanoparticles and restrains the agglomeration of NFVP. • The NFVP/PPC composite displays an outstanding rate performance and cycle stability. Na super-ion conductor type material Na 3 V 2 (PO 4) 3 has been widely researched as the cathode of sodium-ion batteries (SIBs) in recent years, but the unsatisfying cost of Na 3 V 2 (PO 4) 3 impedes its wide application in SIBs. In this study, iron element is used to replace part of vanadium in Na 3 V 2 (PO 4) 3 to reduce its expense, and pine pollen is applied for the first time as a very effective carbon source to improve the performance of Na 4 FeV(PO 4) 3. The fabricated composite material achieves a capacity of 105 mA h g−1 under 0.2 C and fascinating cycling stability over 94 % under 2 C for 500 cycles and 98 % under 10 C for 1000 cycles. The excellent cycle performance is caused by the involvement of pine pollen that acts as a carbon matrix to enhance the electron conductivity and block the agglomeration of active material effectively, thus the well-dispersed nano sized Na 4 FeV(PO 4) 3 shortens the diffusion path of sodium ion and gains a remarkable rate capability. Moreover, the distinguished reversibility during the charge and discharge procedures is ascribed also to the robust structure of Na 4 FeV(PO 4) 3. This work provides an efficient route to realize the economic cathode material of SIBs with good performance. [ABSTRACT FROM AUTHOR]

This study presents a novel method to determine the kinetics of spherical agglomeration in-line via monitoring the stirrer torque. In order to confirm that the torque can be used to characterise the process phases, samples were taken at different times during the agglomeration process and the morphology of agglomerates is examined using X-ray microtomography. It can be shown that if the stirrer torque is decreasing, the fast growth regime starts. Additionally, the influence of binding-liquid concentration as well as the primary particle shape was studied. Both have an influence on the process kinetics as well as on the different growth mechanisms of agglomerates during spherical agglomeration. These two growth mechanisms, distribution and immersion, can be identified by the morphological parameters sphericity, packing density and fractal dimension. In particular, the concept of fractal dimension was not used so far on agglomerates obtained from spherical agglomeration. [ABSTRACT FROM AUTHOR]

The present work explores a systematic investigation of the microstructural, optical, and dielectric properties of W1−xNixO3 (x = 0, 0.02, 0.04, and 0.06) samples and their application in supercapacitors. The sol–gel auto-combustion process was used to synthesize these samples, and a number of analytical techniques such as x-ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, Raman, Scanning Electron Microscopy (SEM), UV–visible spectroscopy, dielectric measurements, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) were used to characterize them. The Rietveld refined XRD patterns confirm the monoclinic phase with space group P21/n in a single phase. FTIR spectroscopy confirms the functional groups associated with stretching and bending vibrational modes at various wavenumbers. Raman spectroscopy ensures the phase purity of the materials and shows a blue shift with Ni doping. SEM microscopy reveals a uniform surface morphology as well as particle agglomeration at the surface. UV–visible studies reveal a significant decrease in the bandgap (2.13–1.81 eV) as the Ni concentration is increased. Dielectric studies show that as the frequency rises, the dielectric constant decreases and becomes saturated at higher frequencies. The highest value of the dielectric constant (ε') is observed for the 4% Ni-doped WO3 sample. The electrochemical and capacitive properties have been characterized and studied using CV and EIS analysis. Cyclic voltammetry tests were carried out in the range of − 0.2 to 0.8 V with varying scan rates (5–100 mVs−1), exhibiting a significantly large area under the CV curve, hence higher values of specific capacitance. The maximum specific capacitance at a scan rate of 5 mVs−1 for each sample of W1−xNixO3 (x = 0, 0.02, 0.04, and 0.06) is found to be 126.671, 192.31, 278.52, and 128.58 Fg−1, respectively, in 2M KOH electrolyte. Thus, the synthesized samples exhibit potential for application as electrode materials for supercapacitors. [ABSTRACT FROM AUTHOR]

The redistribution of electrons is driven by the electric field at the heterogeneous interface, optimizing the electronic structure of the anode material and improving the reaction kinetics. This optimization contributes to the enhanced sodium storage performance of transition metal selenides with the dual-carbon-confined strategy. [Display omitted] Transition metal selenides (TMSs) stand out as a promising anode material for sodium-ion batteries (SIBs) owing to their natural resources and exceptional sodium storage capacity. Despite these advantages, their practical application faces challenges, such as poor electronic conductivity, sluggish reaction kinetics and severe agglomeration during electrochemical reactions, hindering their effective utilization. Herein, the dual-carbon-confined CoSe 2 /FeSe 2 @NC@C nanocubes with heterogeneous structure are synthesized using ZIF-67 as the template by ion exchange, resorcin-formaldehyde (RF) coating, and subsequent in situ carbonization and selenidation. The N -doped porous carbon promotes rapid electrolyte penetration and minimizes the agglomeration of active materials during charging and discharging, while the RF-derived carbon framework reduces the cycling stress and keeps the integrity of the material structure. More importantly, the built-in electric field at the heterogeneous boundary layer drives electron redistribution, optimizing the electronic structure and enhancing the reaction kinetics of the anode material. Based on this, the nanocubes of CoSe 2 /FeSe 2 @NC@C exhibits superb sodium storage performance, delivering a high discharge capacity of 512.6 mA h g−1 at 0.5 A g−1 after 150 cycles and giving a discharge capacity of 298.2 mA h g−1 at 10 A g−1 with a CE close to 100.0 % even after 1000 cycles. This study proposes a viable method to synthesize advanced anodes for SIBs by a synergy effect of heterogeneous interfacial engineering and a carbon confinement strategy. [ABSTRACT FROM AUTHOR]

Spatially dual-confined Ni-dope CoS 2 @NC@C microrods (Ni-CoS 2 @NC@C) are developed via structural design, heteroatom doping and carbon confinement to boost sodium storage performance of the material. [Display omitted] Currently, conversion-type transition metal sulfides have been extensively favored as the anodes for sodium-ion batteries due to their excellent redox reversibility and high theoretical capacity; however, they generally suffer from large volume expansion and structural instability during repeatedly Na+ de/intercalation. Herein, spatially dual-confined Ni-doped CoS 2 @NC@C microrods (Ni-CoS 2 @NC@C) are developed via structural design, heteroatom doping and carbon confinement to boost sodium storage performance of the material. The morphology of one-dimensional-structured microrods effectively enlarges the electrode/electrolyte contact area, while the confinement of dual - carbon layers greatly alleviates the volume change-induced stress, pulverization, agglomeration of the material during charging and discharging. Moreover, the introduction of Ni improves the electrical conductivity of the material by modulating the electronic structure and enlarges the interlayer distance to accelerate Na+ diffusion. Accordingly, the as-prepared Ni-CoS 2 @NC@C exhibits superb electrochemical properties, delivering the satisfactory cycling performance of 526.6 mA h g−1 after 250 cycles at 1 A g−1, excellent rate performance of 410.9 mA h g−1 at 5 A g−1 and superior long cycling life of 502.5 mA h g−1 after 1,500 cycles at 5 A g−1. This study provides an innovative idea to improve sodium storage performance of conversion-type transition metal sulfides through the comprehensive strategy of structural design, heteroatom doping and carbon confinement. [ABSTRACT FROM AUTHOR]

The formulation fundamentally determines the combustion characteristics and agglomeration behavior of propellants. This study compared the effects of four factors on the combustion, agglomeration, and combustion efficiency of nitramine solid propellants: the aluminum size, the ammonium perchlorate size, the nitramine size, and the mass ratio of ammonium perchlorate to nitramine. The comparison was conducted through a series of experimental methods including burning rate tests, collection of the condensed-phase combustion products, chemical titration, and physicochemical analysis. In terms of burning rate, reducing the particle sizes of aluminum powder and ammonium perchlorate, increasing the nitramine size, and increasing the mass ratio of ammonium perchlorate to nitramine all effectively enhance the burning rate. The influence of these four factors on burning rate, in descending order of impact, is: the mass ratio of ammonium perchlorate to nitramine > the ammonium perchlorate size > the aluminum size > the nitramine size. Regarding agglomeration and combustion efficiency, increasing the particle sizes of aluminum and nitramine, increasing the mass ratio of ammonium perchlorate to nitramine, and decreasing the ammonium perchlorate size can effectively inhibit agglomeration and enhance combustion efficiency. Among these, the ammonium perchlorate size has the greatest effect on enhancing the combustion efficiency, potentially increasing it by 16%. The nitramine size has the weakest impact on combustion efficiency, with a potential increase of 5.5%. The experimental results of this study can provide references for a deeper understanding of the combustion mechanisms of nitramine solid propellants, the establishment of combustion models, and the realization of formula optimization. • Formulation effect on combustion and agglomeration of propellants are studied. • The mass ratio of AP to nitramine has the greatest effect on the burning rate. • The AP size has the greatest effect on enhancing the combustion efficiency. • The comprehensive mechanism of formulation on propellants is proposed. [ABSTRACT FROM AUTHOR]

This work focuses on the enhancement of removal performance of TiO2 by the introduction of trace amout of GO composite. Among various synthesis methods, it was found that the GO–doped TiO2 by microwave-assisted hydrothermal method had the highest performance in the improvement for Cr (VI) treatment. The removal rate of Cr (VI) by TiO2–GO (0.05%) was 95.96% which is 13.58% higher than that of TiO2. It can be confirmed that GO was successfully doped on TiO2 by XRD, XPS, and FT-IR characterizations. In addition, SEM, TEM, N2 adsorption isotherm, UV–Vis spectra, and photocurrent response elucidate the mechanism of potency enhancement. The addition of trace GO reduces the particle size of TiO2 and results in the agglomeration phenomenon of TiO2, so that the specific surface area of TiO2 becomes larger and the distribution is more uniform, which expands the photoresponse range, and elevating the photoelectron response. Thus, the absorption ability of visible light is greatly improved. The reported method provides a more economical option for treating Cr(VI) wastewater. [ABSTRACT FROM AUTHOR]

Hydrogen (H 2) is a significant alternative energy supply due to its outstanding and potentially useful properties, promoting sustainable development. Photocatalytic H 2 generation from H 2 O employing inexhaustible and naturally abundant solar power on semiconducting photocatalysts is a promising and sustainable approach. Yet, particle aggregation/agglomeration, insufficient solar-light absorbance capacity, and quick photo-excited charge carriers' recombination are the main deficiencies in most current photocatalytic systems. This investigation intends to fabricate mesoporous YVO 4 nanosheets through a facile hydrothermal process, employing polyvinyl alcohol polymer as a structural directing agent to prevent agglomeration. Moreover, for the first time, varied tiny contents of platinum oxide (PtO) ranging from 0.3 to 1.2 wt%, were decorated on YVO 4 , constructing p-n PtO-YVO 4 heterojunctions. The fabricated catalysts were characterized via advanced instruments and applied to H 2 production using visible light energy. It was found that the physicochemical characteristics of the designed catalysts revealed the influence of loading PtO on the surface, structure, light absorbance features, charge separation, and efficacy. The loading of 0.9 wt% PtO on YVO 4 has barely lowered the surface area (SA) from 187 to 176 m2/g. In contrast, the visible wavelength uptake is notably extended owing to the substantial energy bandgap narrowing from 3.40 to 2.11 eV. The visible-light-evolved hydrogen on 0.9 wt% PtO-YVO 4 amounted to 34.76 mmol g−1. Moreover, this novel sample demonstrated a 99.88% recycling capacity after five cycles. This efficacious photocatalytic H 2 generation is due to extensive light sensitivity and the rapid charge separation and migration between PtO and YVO 4 following the p-n heterojunction mechanism. [Display omitted] [ABSTRACT FROM AUTHOR]

Boronized Ti6Al4V/FHA composites were prepared by microwave sintering of mixed powders of Ti6Al4V, TiB 2 , and synthesized fluorine-substituted hydroxyapatite (FHA) with variable compositions at 1050 °C for 30 min. The unique "lens effect" of microwave facilitated the in-situ transformation of nanoscale TiB 2 into TiB, serving as the reinforcing phase within the composites. Increasing the theoretical fluorine substitution percentage of FHA from 0% to 50% caused less thermal decomposition of hydroxyapatite during sintering, promoting densification and thereby mechanical properties of the composites. However, elevating the substitution percentage to 100% led to excessive grain growth and FHA agglomeration, deteriorating the composite mechanical performance. The boronized Ti6Al4V/FHA composite produced using FHA with the theoretical fluorine substitution of 50% exhibited the highest compressive strength (397.7 MPa), proper compressive modulus (10.65 GPa) and maximum microhardness (385.3 HV). Furthermore, it showed excellent hydrophilicity and good cell adhesion, confirming its superior bioactivity for dental applications. [Display omitted] [ABSTRACT FROM AUTHOR]

Fiber is highly escapable in conventional slickwater, making it difficult to form fiber-proppant agglomerate with proppant and exhibit limited effectiveness. To solve these problems, a novel structure stabilizer (SS) is developed. Through microscopic structural observations and performance evaluations in indoor experiments, the mechanism of proppant placement under the action of the SS and the effects of the SS on proppant placement dimensions and fracture conductivity were elucidated. The SS facilitates the formation of robust fiber-proppant agglomerates by polymer, fiber, and quartz sand. Compared to bare proppants, these agglomerates exhibit reduced density, increased volume, and enlarged contact area with the fluid during settlement, leading to heightened buoyancy and drag forces, ultimately resulting in slower settling velocities and enhanced transportability into deeper regions of the fracture. Co-injecting the fiber and the SS alongside the proppant into the reservoir effectively reduces the fiber escape rate, increases the proppant volume in the slickwater, and boosts the proppant placement height, conveyance distance and fracture conductivity, while also decreasing the proppant backflow. Experimental results indicate an optimal SS mass fraction of 0.3%. The application of this SS in over 80 wells targeting tight gas, shale oil, and shale gas reservoirs has substantiated its strong adaptability and general suitability for meeting the production enhancement, cost reduction, and sand control requirements of such wells. [ABSTRACT FROM AUTHOR]

We have obtained straight-line-shaped agglomeration grooves of 2~3.5 μm width in the ~60-nm-thick Si thin films by the continuous-wave laser crystallization (CLC) when the laser power is increased above the optimum power to obtain grain boundary-free (GB-free) films. The GB-free CLC is suitable for fabricating monolithic three-dimensional integrations. The grooves are formed in the Si film vertically from the Si surface to the underlying insulating substrate, and a hump of the Si film is generated along the edge of the groove at the retarded side of the scan. In situ observation of the crystal growth shows that the grooves originate from voids, which happen to be generated by agglomeration in the melt zone. The voids move at a constant velocity, Vvoid , within the melt zone. The melt zone moves at the scan velocity, V, to the scan direction. The void velocity, Vvoid , is obtained from the angle of the groove line to the scan direction, and is found to be proportional to V−0.5. [ABSTRACT FROM AUTHOR]

Based on the land economic density of 892 town units, the spatial pattern of the land economic density in Zhejiang Province is analyzed using the coefficient of variation, spatial classification, and spatial correlation methods, and the influencing factors are analyzed using a spatial regression model. The results are as follows: (1) The coefficients of variation were 2.6 and 3.1 in 2014 and 2019, respectively, indicating that the degree of imbalance of the town's industrial economy at the county level increased. (2) The distribution of the high-level agglomeration areas was characterized by one core area and two sub-core areas. The main core area was located at the junction of Hangzhou City, Shaoxing City, and Jiaxing City, and the two sub-core areas were located in Yuyao City and the main urban area of Ningbo City. In addition, several small-scale agglomeration areas composed of medium and high-level units were distributed in Wenzhou City. (3) The high-value agglomeration and low-value agglomeration distribution in the spatial correlation patterns was identified using the spatial auto-correlation method. The hot spots and sub-hot spots were distributed in Northern Zhejiang, and the cold spots formed a large-scale agglomeration in Quzhou City, Lishui City, Taizhou City, and several other cities in Southern Zhejiang. (4) Compared with the county scale, the spatial scope of the high-level areas in Northern Zhejiang shrunk significantly at the township scale, and the high-level agglomeration areas along the southeast coast changed into a cluster of several townships. (5) According to the geographically weighted regression (GWR) model, the importance of influencing factors is as follows: population density > regional area > industrial output value per capita > total population > proportion of secondary and tertiary personnel > total employees. [ABSTRACT FROM AUTHOR]

Herein, the spatial evolution characteristics of high-level Grade A tourist attractions in the Yangtze River Delta (YRD) urban agglomeration, from 2001 to 2021, are studied by comprehensively applying the nearest neighbor index, kernel density analysis, standard deviation ellipse, and spatial autocorrelation. High-level Grade A tourist attractions are investigated using the random forest model as the driving mechanism of the spatial pattern. Results show that 1) the spatial distribution of high-level Class A tourist attractions in the YRD city cluster has grown to be an agglomeration, and the high-density areas have evolved from "point-like dispersion to regiment-like combination," gradually forming a B-shaped core density structure. 2) The spatial distribution comprises an overall "northwest–southeast" direction, a small counterclockwise rotation, the distribution of the center of gravity to the southwest migration, and the center of gravity from the territory of Suzhou City to the territory of Huzhou City. 3) The high-level Class A tourist attractions in the YRD city cluster as a whole show a strong positive spatial correlation, and the significantly clustered areas include three types: high-high (H-H), low-low (L-L), and low-high (L-H). 4) The spatial distribution of high, A-level tourist attractions in the YRD city cluster results from the combined action of the natural environment, resource endowment, socioeconomy, and policy background. Each element has a nonlinear and complex influence on the distribution of scenic spots. [ABSTRACT FROM AUTHOR]

Pulverized coal pyrolysis based on solid heat carrier has a huge advantage in high tar yield. In this study, pyrolysis experiments on pulverized coal were conducted in a lab-scale fluidized bed reactor at 650 °C, utilizing char as the solid heat carrier. The influence of mass ratio of char to coal (RATIO) was investigated. Results show that the incorporation of solid heat carrier of char significantly enhanced the primary pyrolysis reaction in coal pyrolysis, resulting in increasing yields of tar and gas but reducing one of char. The yield of tar maximally reached 148.80–262.22% of the Gray–King analysis value at the RATIO of 14.52 g/g. As the RATIO increased, the tar contained more light component content, indicating that incorporating solid heat carriers improved the tar quality. These findings offer significant insights for the design of fluidized bed pyrolysis unit utilizing char as solid heat carrier. [ABSTRACT FROM AUTHOR]

Ti3C2Tx MXene, as a common two-dimensional material, has a wide range of applications in electrochemical energy storage. However, the surface forces of few-layer or monolayer Ti3C2Tx MXene lead to easy agglomeration, which hinders the demonstration of its performance due to the characteristics of layered materials. Herein, we report a facile method for preparing monolayer Ti3C2Tx MXene on nickel foam to achieve a self-supporting structure for supercapacitor electrodes under high electrostatic fields. Moreover, the specific capacitance varies with the deposition of different-concentration monolayer Ti3C2Tx MXene on nickel foam. As a result, Ti3C2Tx/NF has a high specific capacitance of 319 mF cm−2 at 2 mA cm−2 and an excellent long-term cycling stability of 94.4% after 7000 cycles. It was observed that the areal specific capacitance increases, whereas the mass specific capacitance decreases with the increasing loading mass. Attributable to the effect of the high electrostatic field, the self-supporting structure of the Ti3C2Tx/NF becomes denser as the concentration of the monolayer Ti3C2Tx MXene ink increases, ultimately affecting its electrochemical performance. This work provides a simple way to overcome the agglomeration problem of few-layer or monolayer MXene, then form a self-supporting electrode exhibiting excellent electrochemical performance. [ABSTRACT FROM AUTHOR]

The combination of hollow micromorphology and graphene anchoring effectively alleviate the volume changes during cycling, greatly improves the electronic conductivity and inhibit the agglomeration and pulverization of the material, the H-VO 2 @GO exhibits excellent electrochemical properties. [Display omitted] Vanadium dioxide-based materials have been proved to be promising cathodes for aqueous zinc ion batteries (AZIBs) due to their cost-effectiveness and high theoretical specific capacity; nevertheless, the low electronic conductivity and poor cycle stability restrict their application. Herein, hollow VO 2 microspheres anchored on graphene oxide (H-VO 2 @GO) are synthesized via a facile simple hydrothermal reaction as high-performance cathodes for AZIBs. The hollow micromorphology of the material provides a large specific surface area and effectively alleviates the volume changes during cycling, while the anchoring of VO 2 on graphene oxide greatly improves the electronic conductivity and inhibits the agglomeration and pulverization of the material. Resulting from the combination of unique micromorphology and graphene oxide anchoring, the as-prepared H-VO 2 @GO exhibits the impressive specific capacity of 400.1 mAh/g at 0.5 A/g and excellent cycling performance with 96.1 % of capacity retention after 1500 cycles at 10 A/g. This investigation provides a use reference for designing high-performance cathodes materials for AZIBs by optimizing the microstructure of electrode materials. [ABSTRACT FROM AUTHOR]

Here in the present work, simple, eco-friendly and economical method of synthesis has been approached known as hydrothermal synthesis that allowed easy doping of Fe ions into the ZnS host lattice. A unique approach was adopted for the first time to prepare ZnS material where thioglycolic acid (TGA) was used as a source for sulfur in addition to a reducing and capping agent. Properties of the nanostructures were explored using different techniques. The X-ray diffraction (XRD) results indicated formation of single phase hexagonal ZnS material where inclusion of Fe2+ ions into the ZnS lattice have no influence on the crystal phase of the material. Probably almost identical sizes of Zn2+ and Fe2+ ions made this possible that indicated Fe2+ ions take Zn2+ vacant sites by substitution of Zn2+ ions by Fe2+ ions. Chemical analysis (X-ray photoelectron spectroscopy) performed discovered that Zn and Fe ions were present in +2 oxidation states whereas S is in −2 state. Anisotropic growth of the nanostructures is reported where irregular shaped nanostructures of varying dimensions were formed that agglomerated as doping concentration was increased to form spherical microstructures. Inclusion of Fe ions into the host material modified magnetic behavior of the nanostructures converting diamagnetic ZnS into a ferromagnetic material. Optical properties were also influence by the doping resulting in photon absorption at different wavelengths. The band gap got reduced from 3.2 eV to 2.7 eV making the ZnS nanostructures visible light active. The nanostructures with band gap 2.7 eV exhibited good photocatalytic activity against methylene blue (MB) dye under visible light illumination degrading 94% of the dye in just 2 h. The scavenging experiments performed showed hydroxyl free radicals play an active role in mineralizing the dye. Reusability and post photocatalytic properties of the photocatalysts determined their stability and potential ability for possible commercialization. [ABSTRACT FROM AUTHOR]

We evaluated the effect of O atoms on the postannealed BaSi2 films grown by molecular beam epitaxy. Postannealing (PA) in an Ar atmosphere at a pressure of 1.9 × 105 Pa increased the O concentration to 7 × 1020 cm−3 in the bulk region and further increased to ∼1022 cm−3 at the BaSi2/Si interface. Cracks formed during the PA process, allowing O to enter more easily to the BaSi2 films. In the x-ray photoelectron spectroscopy spectrum of the Si 2s core level measured at 10 nm from the surface, a shift of the peak related to SiOx was detected, indicating a change in the bonding state of Si and O in this region. When PA was performed in vacuum at 10−3 Pa, the photoresponsivity in the short wavelength region was enhanced, with a maximum value of 6.6 A W−1 at 790 nm. The O concentration in the film decreased in the sample annealed in vacuum, and the PL peak intensity at 0.85 eV decreased, suggesting that this was due to a decrease in O-related defects compared to the Ar atmosphere. However, agglomeration of BaSi2 caused significant surface roughness, indicating the importance of PA conditions that minimize O uptake and keep the surface smooth for improved performance of BaSi2 solar cells. [ABSTRACT FROM AUTHOR]

CILRT is an important work in the overhaul of nuclear power plants. VOCs from paints and cleaners used in the containment during the overhaul will migrate inside the containment, and the numerous rooms and compartments inside the containment make the air flow impeded, and the VOCs may be enriched to bring combustion risk. The complete fire risk analysis method includes volatilization kinetics of chemicals, mixture explosion limits, and numerical simulation of VOCs diffusion and migration. The volatilization rate at the lowest room temperature of 20°C is used as a conservative input, the complement of CAITA realistic model is used as the flow domain, and the geometry is appropriately simplified, and the steady ventilation process, the internal flow and the laws of diffusion and agglomeration of 12 kinds of VOCs gases in the 9-h pressure-holding process are investigated by Computational Fluid Dynamics. The simulation results of steady ventilation show that the VOCs gases are almost uniformly carried by the air to all spaces inside the containment, and the explosion risk is low. The concentration field of the steady ventilation process was taken as the initial boundary condition and unsteady state simulation of the 9-h holding pressure process was performed. The results show that the gas flow inside the containment basically stops after 3456 s of pressure holding. With the extension of time, the VOCs gases accumulate at the bottoms of the three lower layers of the containment under the effect of laminar diffusion and gravitational settling, where the total concentration of the mixed gases reaches the highest at the bottom of the lowest layer. The total concentration of the VOCs gas mixture was below the lower explosion limit throughout the 9-h pressure-holding process, and the explosion risk was low. [ABSTRACT FROM AUTHOR]

As highly concentrated urbanized areas, urban agglomerations bear increasing resource depletion and environmental pressures, which threaten the regional sustainable development. Resource and environmental problems arising from the process of urbanization can be attributed to the dislocation or maladjustment of material metabolism in time or space. Conducting research on material metabolism at the level of urban agglomerations is helpful in finding the root causes of environmental problems to provide support for the reduction of regional resource consumption and pollution emissions. The material metabolism characteristics of the urban agglomeration and internal cities of the Fujian Delta Urban Agglomeration (FDUA) in China are evaluated using the material flow analysis. The following results are observed. (1) The economic development of the FDUA is still at risk of resource consumption, and a large proportion of hidden flow (HF > 80%) drags down the overall metabolic efficiency and sustainable development. (2) The discharge of various pollutants in the FDUA generally shows a downward trend. Improving metabolic efficiency, delayed MCI growth, and improved overall regional environmental quality are observed. (3) Cities that have relatively scarce land resources but are economically developed, such as Xiamen, still bear a relatively heavy ecological burden (ECdmc > 1). (4) Regional collaboration is conducive to the sustainable development of multiple regions. On the one hand, the results of this study provide decision-making basis for the sustainable development of the national ecological civilization demonstration area. On the other hand, this work guides the establishment of a comprehensive industrial linkage and cooperation mechanism for the same type of small- and medium-sized urban agglomerations. [ABSTRACT FROM AUTHOR]

The aim of this research was to measure the filtration properties of waste coal ash under the influence of hydrostatic pressure generated in a three-axial compression apparatus. The scope of work included determining the compactibility parameters, maximum bulk density and optimal moisture content. Permeability tests were performed for a sample with an average grain composition at three compaction indices I S : 0.964, 0.98 and 1.00. The hydrostatic pressure ranging from 0.5 to 1.8 bar corresponded to the layer depths from 2.17 to 7.83 m. Gradually increasing the pressure during the first loading cycle caused irreversible changes in the structure of the sample by local material agglomeration or grain interlocking. The water permeability coefficient was higher in the second loading cycle than in the first cycle. It was shown that waste coal ash cannot be used as a construction material on its own. To obtain constant filtration properties, the waste coal ash material should be doped, or an optimal compactionshould be used ( I S = 1.00). The results presented in this study are important for assessing the use of waste coal ash for construction engineering purposes. [ABSTRACT FROM AUTHOR]

Thermal energy storage utilizing the adsorption of moisture from air is a promising energy storage technology due to its high energy density and minimum heat losses. Salt hydrates and salt hydrate composites, such as calcium chloride (CaCl2) and CaCl2-based composites, have shown favourable energy storage properties in this area of research. However, these materials have shown issues with stability due to swelling and deliquescence. In this work, CaCl2 was stabilized using three methods: impregnation into silica gel, encapsulation in methyl cellulose, and both impregnation and encapsulation stabilization techniques used simultaneously. Therefore, three CaCl2-based composites were synthesized. For the first composite, silica gel was impregnated with CaCl2. For the second composite, CaCl2 was encapsulated by methyl cellulose. For the third composite, silica gel was impregnated with CaCl2 and the CaCl2 was encapsulated with methyl cellulose. These samples were structurally characterized using scanning electron microscopy as well as Brunauer-Emmett-Teller (BET) to determine surface area, pore size distribution and nitrogen adsorption isotherms at 77 K. Water vapour adsorption isotherms were also determined at 25 °C for different relative humidities by dynamic vapor sorption (DVS). Similarly, LiCl-based composites were also synthesized and examined in this work, but issues of deliquescence, swelling, and agglomeration made the materials impractical to work with. To determine the prepared materials' thermal energy storage performance, 2–6 g of each sample was tested in a lab-scale apparatus. This process uses the exothermic adsorption of moisture from ambient air in an open thermal energy storage system. The CaCl2 impregnated silica gel that was encapsulated in methyl cellulose showed reasonably high stability and energy storage performance after 3 hydration and dehydration cycles with minimum agglomeration. An energy storage density of 241 kWh/m3 (0.87 GJ/m3) and specific energy of 630 Wh/kg (2268 kJ/kg) was achieved with this material for 90% inlet relative humidity after a regeneration at 90 °C. [ABSTRACT FROM AUTHOR]

The article presents the results of experimental studies on the gasification of mixtures of brown coal and polyethylene (up to 20 wt% fraction) in a laboratory reactor. The work aims to study the agglomeration process during the heating and oxidation of the mixtures. The measurement results (gas composition, pressure drop) provide indirect information on the dynamics of thermal decomposition and structural changes in the fuel bed. We have shown that the interaction between polyethylene and a coal surface leads to the formation of dense agglomerates, in which the molten polymer acts as a binder. Clinkers form as a result of interfacial interactions between components and filtration flow rearranging. The hydrogen/carbon ratio in the solid residue of coal-polyethylene co-gasification increases from 0.07–0.2 to 1.11, indicating the formation of stable hydrocarbon compounds on the carbon surface. The conducted research makes it possible to identify possible interactions between chemical reactions and transfer processes that lead to agglomeration in mixtures of coal with polyethylene. [ABSTRACT FROM AUTHOR]

In order to address the issue of magnetic agglomeration leading to poor magnetic separation efficiency and low activity enhancement, resulting in limited utilization of steel slag fine powder material, this study proposes a novel dry magnetic separator with air fluidization as the feeding method. The new separator incorporates adjustable magnetic field strength based on the material's magnetic properties, enabling individual particle separation through a magnetic mesh while simultaneously enhancing mechanical and ultrasonic composite vibration. In addition, it enhances competitiveness by incorporating negative pressure suction. Primary magnetic separation tests on a steel slag fine powder material demonstrate that the air fluidized dry magnetic separator effectively separates inert minerals from active minerals in the steel slag powder. The iron grade in the magnetic products reaches 21.81%, which is 6.88% higher than that of the original steel slag, while the iron grade in non-magnetic products decreases to 11.93%, representing a 3% reduction compared to the original steel slag composition. Further sweeping and selection processes are expected to further improve these results, ultimately achieving effective utilization of steel slag. [ABSTRACT FROM AUTHOR]

Given its wide application ranges, dielectric capacitors have garnered extensive attentions. However, due to the excessive premature agglomeration of free electrons, capacitors with nanocomposites as dielectrics fail to attain high breakdown strength (E b), and thereby constrain their ability to achieve superior energy storage performances. To alleviate the effects of free electrons and secondary impact-ionized electrons (SIE) on E b and leakage currents, here, a novel organic-inorganic core–shell Ni(OH) 2 @PDI (N@P) nanofiller with opposite double-PN-junction was well-designed and successfully synthesized by coating p-typed Ni(OH) 2 nanosheets with n-typed perylene diimide (PDI). It could reduce free electron kinetic energy and mitigate SIE amounts regardless of the applied electric field direction. Furthermore, PDI, as an organic compound, can uniformly and densely coat onto surfaces of 2D Ni(OH) 2 , as well as enhance compatibilities between Ni(OH) 2 and matrix, and thereby reducing structure defects at their interfaces. Last but not the least, Ni(OH) 2 nanosheets also contribute to E b improvement via acting as scattering centers. Experimental and simulation results concurrently affirmed positive influences of organic-inorganic N@P nanofillers on discharge energy density (U d) and efficiency (η) of P(VDF-HFP)-based (PVH-based) nanocomposites. Remarkably, 1.3 vol% N@P/PVH achieves a high U d of 21.7 J/cm3 and η of 81.2 % under 569.0 MV/m. More importantly, it maintains an excellent energy storage performance throughout 104 cyclic tests. This study presents a valid strategy for concurrently improving U d and η of polymer-based nanocomposites. [ABSTRACT FROM AUTHOR]

Copyright of Environmental & Social Management Journal / Revista de Gestão Social e Ambiental is the property of Environmental & Social Management Journal and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Sol-gel dip-coating deposition was used to create Zr-doped Bi 2 O 4 thin films with Zr in the range of 1-5 wt%. The monoclinic Bi 2 O 4 phase was confirmed by an X-ray diffraction (XRD) analysis. After Zr doping in Bi 2 O 4 , there was a minor change in crystallite size and a reduction in the lattice parameters. UV-VIS-NIR spectrophotometry showed a decrease in the band gap of Bi 2 O 4. These films were useful as absorbing layers for solar cells due to their decreased band gap, which allowed them to absorb a wide range of visible portions of the electromagnetic spectrum. SEM micrographs for each film showed an almost spherical-like appearance. The agglomeration of Bi 2 O 4 into bigger particles with a lower surface area may be the cause of the decrease of the dielectric constant with an increase in Zr concentration. The AC conductivity of thin films increased with an increase in Zr concentration. Electrochemical charge-discharge test findings revealed the specific capacitance, power density, and energy of Zr-doped Bi 2 O 4. Magnetic measurements of Zr-doped Bi 2 O 4 nanostructures revealed ferromagnetic ordering at the surrounding temperature. The rise in saturation magnetization that occurred with an increase in Zr doping emerged from the formation of defects in the Bi 2 O 4 lattice caused by oxygen vacancies and structural inhomogeneity, which promoted the growth of bound magnetic polarons. Additionally, Zr doping improved the photocatalytic qualities of Bi 2 O 4. The enhanced photocatalytic activity of Zr-doped Bi 2 O 4 nanoparticles was attributed to the higher UV-VIS light absorption and the reduced recombination rate of the photoinduced electron-hole pair making it a promising substance for water filtration. When Bi 2 O 4 was combined with Zr, it inhibited the growth of Staphylococcus aureus (S. aureus), which was gram-positive while, Klebsiella pneumoniae (K. pneumoniae), Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli) were gram-negative bacterial stains. Zr doping in Bi 2 O 4 improved its antibacterial action. [ABSTRACT FROM AUTHOR]

Cobalt zinc chromium ferrites, which have been doped with chromium Co0.4Zn0.6-xCrxFe2O4 (x = 0.05, 0.10, 0.15, 0.20) (CZC) nanoferrites, are employed by the auto-combustion route. The magnetic and dielectric characteristics of Co–Zn nanoferrites were improved by Cr3+. Analysis using XRD, FTIR, and FESEM reveals the cubic spinel phase for CZC nanoferrites. SEM reveals a lot of clustering. The ferrite samples have cluster form with a spherical shape in the range 54.64–73.38 nm, as seen by the FESEM results. TEM studies show agglomeration. The Cr3+ concentration determines the magnetic properties of specimens. Ms declines from 62.38 emu/g to 42.59 emu/g by increasing Cr3+. For all samples, a frequency-dependent evaluation of the dielectric properties, including dielectric constant, dielectric loss, and ac conductivity, is performed. On the basis of Koop's theory, the Maxwell-Wagner polarization procedure, and the movement of electrons, the fluctuation of dielectric features at frequencies between 50 Hz and 108 Hz has been mentioned. The dielectric constant and dielectric loss tangent decreased with increasing frequency. The conduction of ferrite samples is influenced by the grain boundaries. Both recording media and high-frequency devices can benefit from using these nanoferrites. [ABSTRACT FROM AUTHOR]

Oncolytic Newcastle disease virus is a new type of cancer immunotherapy drug. This paper proposes a scheme for delivering oncolytic viruses using hydrogel microneedles. Gelatin methacryloyl (GelMA) was synthesized by chemical grafting, and GelMA microneedles encapsulating oncolytic Newcastle disease virus (NDV) were prepared by micro-molding and photocrosslinking. The release and expression of NDV were tested by immunofluorescence and hemagglutination experiments. The experiments proved that GelMA was successfully synthesized and had hydrogel characteristics. NDV was evenly dispersed in the allantoic fluid without agglomeration, showing a characteristic virus morphology. NDV particle size was 257.4 ± 1.4 nm, zeta potential was −13.8 ± 0.5 mV, virus titer TCID50 was 107.5/mL, and PFU was 2 × 107/mL, which had a selective killing effect on human liver cancer cells in a dose and time-dependent manner. The NDV@GelMA microneedles were arranged in an orderly cone array, with uniform height and complete needle shape. The distribution of virus-like particles was observed on the surface. GelMA microneedles could successfully penetrate 5% agarose gel and nude mouse skin. Optimal preparation conditions were freeze-drying. We successfully prepared GelMA hydrogel microneedles containing NDV, which could effectively encapsulate NDV but did not detect the release of NDV. [ABSTRACT FROM AUTHOR]

The introduction of S induces a large number of Se vacancies in iron selenide, adjusts the electronic structure of iron selenide, reduces the Na+ diffusion barrier, and optimizes the sodium storage performance of iron selenide together with the carbon confinement strategy. [Display omitted] • Se vacancies adjust the electron density and improve the conductivity of material. • Se vacancies promote Na+ migration and enhance the reaction kinetics of material. • The carbon confinement strengthens the structural stability of the electrode. • The material possesses excellent electrochemical properties. Recently, iron selenides have been considered as one of the most promising candidates for the anodes of sodium-ion batteries (SIBs) due to their cost-effectiveness and high theoretical capacity; however, their practical application is limited by poor conductivity, large volume variation and slow reaction kinetics during electrochemical reactions. In this work, spatially dual-carbon-confined V Se -Fe 3 Se 4-x S x /FeSe 2-x S x nanohybrids with abundant Se vacancies (V Se -Fe 3 Se 4-x S x /FeSe 2-x S x @NSC@rGO) are constructed via anion doping and carbon confinement engineering. The three-dimensional crosslinked carbon network composed of the nitrogen-doped carbon support derived from polyacrylic acid (PAA) and reduced graphene enhances the electronic conductivity, provides abundant channels for ion/electron transfer, ensures the structure integrity, and alleviates the agglomeration, pulverization and volume change of active material during the chemical reactions. Moreover, the introduction of S into iron selenides induces a large number of Se vacancies and regulates the electron density around iron atoms, synergistically improving the conductivity of the material and reducing the Na+ diffusion barrier. Based on the aforementioned features, the as-synthesized V Se -Fe 3 Se 4-x S x /FeSe 2-x S x @NSC@rGO electrode possesses excellent electrochemical properties, exhibiting the satisfactory specific capacity of 630.1 mA h g−1 after 160 cycles at 0.5 A/g and the reversible capacity of 319.8 mA h g−1 after 500 cycles at 3 A/g with the low-capacity attenuation of 0.016 % per cycle. This investigation provides a feasible approach to develop high-performance anodes for SIBs via a synergetic strategy of vacancy engineering and carbon confinement. [ABSTRACT FROM AUTHOR]

Copyright of Environmental & Social Management Journal / Revista de Gestão Social e Ambiental is the property of Environmental & Social Management Journal and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

MXene has emerged as a highly promising two-dimensional (2D) layered material with inherent advantages as an electrode material, such as a high electrical conductivity and spacious layer distances conducive to efficient ion transport. Despite these merits, the practical implementation faces challenges due to MXene's low theoretical capacitance and issues related to restacking. In order to overcome these limitations, we undertook a strategic approach by integrating Ti3C2Tx MXene with cobalt molybdate (CoMoO4) nanoparticles. The CoMoO4 nanoparticles bring to the table rich redox activity, high theoretical capacitance, and exceptional catalytic properties. Employing a facile hydrothermal method, we synthesized CoMoO4/Ti3C2Tx heterostructures, leveraging urea as a size-controlling agent for the CoMoO4 precursors. This innovative heterostructure design utilizes Ti3C2Tx MXene as a spacer, effectively mitigating excessive agglomeration, while CoMoO4 contributes its enhanced redox reaction capabilities. The resulting CoMoO4/Ti3C2Tx MXene hybrid material exhibited 698 F g−1 at a scan rate of 5 mV s−1, surpassing that of the individual pristine Ti3C2Tx MXene (1.7 F g−1) and CoMoO4 materials (501 F g−1). This integration presents a promising avenue for optimizing MXene-based electrode materials, addressing challenges and unlocking their full potential in various applications. [ABSTRACT FROM AUTHOR]

In the process of agricultural development in arid and semi-arid areas, the carbon fixation capacity of vegetation can be affected to different degrees, but research on its driving factors is lacking. Consequently, this paper focuses on the Weiku Oasis in Xinjiang as its research area, in which the carbon fixation capacity of vegetation is estimated with the chemical equation of a photochemical reaction, using methods such as linear system models and Geodetector to analyze the relationship between cropland expansion characteristics and the carbon fixation capacity of vegetation from 1990 to 2020. The influence of land-use changes on the space differentiation of carbon fixation was elucidated through a time series relationship, and the synergistic effects of nine influencing factors on the carbon fixation capacity during the process of vegetation changes were discussed. The results were as follows: (1) In the process of agricultural development, the proportions of cultivated land area and spatial agglomeration had significant negative correlations with carbon sequestration, and the significance was rising, but the effect of cultivated land area proportion was more significant. (2) Through temporal sequential cooperativity analysis, when other land-use types were converted into cultivated land, the carbon fixation capacity of vegetation suddenly and significantly decreased in the initial year of the transformation, but the effect of cultivated land reclamation on the carbon fixation capacity of vegetation did not have a significant time lag. Moreover, after a certain period of time, cultivated land can gradually recover part of its lost carbon fixation capacity. (3) Among the nine driving factors, potential evapotranspiration is the most prominent in explaining the carbon fixation capacity of vegetation. This single-factor pairwise interaction presents the relationship between bivariate enhancement and nonlinear enhancement. When terrain factors interact with other factors, the enhancement effect of the influence on the carbon fixation capacity of vegetation has an obvious promotion effect. However, the change in the carbon fixation capacity of vegetation is more significantly influenced by potential evapotranspiration and the interaction between the normalized difference vegetation index (NDVI) and other factors. This research is helpful to understanding the basic theories related to the change in the carbon fixation capacity of vegetation during the process of agricultural development in arid and semi-arid areas, as well as providing theoretical reference for ecological environment construction and sustainable development. [ABSTRACT FROM AUTHOR]

Urban agglomerations are becoming increasingly important in driving economic development in China. Accurate representation of the economic development status and spillover effects of cities within an urban agglomeration is the foundation of and an effective approach for promoting the coordinated development of that agglomeration. However, current studies of economic spillovers tend to focus on urban agglomerations as a whole, and there is a lack of scrutiny and validation of research data. Therefore, this study proposes a framework for detecting economic spillover effects within an urban agglomeration based on a prolonged night-time light dataset. Firstly, we explored the most suitable night-time light index to characterize the economic status. Then, we used this index to construct the economic network and hierarchical structure of the urban agglomeration. Finally, we explored the heterogeneity of spillover effects under the hierarchical structure. The results of a case study in the Pearl River Delta (PRD) urban agglomeration show that (1) the total night-time light in built-up areas (BNTL) has the highest Pearson correlation coefficient with GDP, which is 0.82; (2) there is an obvious hierarchical structure within the PRD; (3) there are significant and sustained economic spillover effects among the core cities, with Guangzhou–Foshan and Shenzhen–Dongguan having more obvious spillover effects; and (4) the economic spillover effects within the three metropolitan areas have different characteristics. The Guangzhou–Foshan–Zhaoqing metropolitan area is closely linked, to apparent differences in the pace of spillover effects. The Shenzhen–Dongguan–Huizhou metropolitan area has strong close linkages, with strong synchronization of spillover effects. The Zhuhai–Zhongshan–Jiangmen metropolitan area has not yet formed a stable synergistic development relationship. Overall, the framework can effectively reveal the hierarchical structure and different characteristics of economic spillovers within urban agglomerations, which can provide a scientific reference for policy making related to the coordinated development of such agglomerations. [ABSTRACT FROM AUTHOR]

Improving the discharge capacities of anode materials for lithium-ion batteries without sacrificing their cycling stability and rate performance at high current densities is a big challenge due to the limited Li+ diffusion kinetics and electronic conductivity. Therefore, the introduction of dissimilar metal ions into the crystal to form doping defects can effectively improve the microstructure and ion transport kinetics, thus significantly increasing the specific capacity. As an example, a new metal ion-substituted Li 2 ZnTi 3 O 8 anode material with low agglomeration and high diffusion coefficient performs a large specific capacity of 112.4 mAh g−1 at 7.0 A g−1 and good cycle stability, as well as outstanding rate performance. The obtained electrochemical performance enhancement can be attributed to guest ions changing the microscopic crystal structure, including the influence of dopant atoms on the surrounding bulk atoms and the creation of vacancies, as well as enlarged ion transport tunnels. This strategy provides an effective way to improve the eXtreme Fast Charging of the lithium-ion battery. [Display omitted] • Li 2 Zn 0.5 M 0.5 Ti 3 O 8 nanoparticles were fabricated via high temperature solid-state technique. • High diffusion coefficient and large specific capacity at 7.0 A g−1 of the Li 2 Zn 0.5 Ni 0.5 Ti 3 O 8 was demonstrated. • This strategy of dissimilar metal ion replacement provides an effective way to improve the LIBs eXtreme Fast Charging. [ABSTRACT FROM AUTHOR]

Herein we demonstrate the influence of aliovalent (Ca2+) substitution in the single-phase orthorhombic La 1-x Ca x FeO 3 (with x = 0.01, 0.03, 0.05, 0.07, 0.09) nanoparticles prepared by simple combustion method. The samples were systematically studied using XRD, SEM-EDS, and UV–Vis-DRS characterization techniques for their structural, microstructural-elemental, and optical (band structure) characteristics. Also, the catalytic attributes were evaluated through photocatalytic studies against indigo carmine in the presence of visible light. It was observed that La 1-x Ca x FeO 3 nanoparticles crystallized in orthorhombic structure at its as-synthesized form. The SEM analysis showed that the spherical nanoparticles with high porosity and agglomerations were further reduced with increasing Ca2+ concentration. The inclusion of Ca2+ also demonstrated the change in the band structure, as the band gap of the material reduced from 2.24 eV to 1.75 eV while the Ca2+ content increased from 1 mol% to 9 mol%. Furthermore, elevating the Ca2+ levels in the La 1-x Ca x FeO 3 resulted in enhanced photocatalytic decomposition of the indigo carmine dye, exhibiting a maximum efficacy of 96.5 % at neutral pH and a stabilization period of 120 min under visible light. The increase in photocatalysis is attributed to the formation of Fe4+ ions and oxygen vacancies induced by the aliovalent cation (Ca2+) replacement at the La3+ site in the LaFeO 3 host matrix. The results suggest that the prepared LaFeO 3 nanoparticles are potential nano-catalysts for photocatalytic activities against indigo carmine under visible light. [ABSTRACT FROM AUTHOR]

Cu-SSZ-39 zeolite with an AEI structure exhibits excellent hydrothermal stability and can be a potential alternative to Cu-SSZ-13 zeolite SCR catalysts for NOx removal in diesel vehicles. However, the inferior low-temperature performance of Cu-SSZ-39 leads to substantial NOx emissions during the cold-start period, impeding its practical application. In this study, Ce-Mn oxide-modified Cu-SSZ-39 catalysts (CeMnOx/Cu-SSZ-39) and references (CeO2/Cu-SSZ-39 and MnOx/Cu-SSZ-39) were prepared by the ion-exchange of Cu ions followed by impregnation of the oxide precursors, with the aim of enhancing the NH3-SCR performance at low temperatures. The modified catalysts exhibited improved low-temperature activity and hydrothermal stability compared to the unmodified counterpart. In particular, CeMnOx/Cu-SSZ-39 showed the highest activity among the three catalysts and achieved NOx conversions above 90% within the temperature range of 180 °C to 600 °C, even after undergoing hydrothermal aging at 800 °C. Experimental results indicated that the synergistic effect between Ce and Mn in CeMnOx improves the redox properties and acidity of the catalyst due to the presence of Ce3+, Mn4+, and abundant adsorbed oxygen species, which facilitate low-temperature SCR reactions. Furthermore, the interaction of CeMnOx with Cu-SSZ-39 stabilizes the zeolite framework and hinders the agglomeration of Cu species during the hydrothermal aging process, contributing to its exceptional hydrothermal stability. The kinetics and NO oxidation experiments demonstrated that CeMnOx provides access to fast SCR reaction pathways by oxidizing NO to NO2, resulting in a significant increase in low-temperature activity. This study provides novel guidelines for the design and preparation of Cu-SSZ-39 zeolite with outstanding SCR performance over a wide temperature range. [ABSTRACT FROM AUTHOR]

The paper presents a granulometric analysis of the size of particles of Aeroxide® P25 and P90 titanium oxides in the context of their retention in low-pressure membrane processes (microfiltration, ultrafiltration). Measurements of the particle size using a laser granulometer showed that the particle size of TiO2 Aeroxide® P25 dispersed in water is in the range from approx. 0.3 µm to approx. 150 µm. The particles with dimensions smaller than 1.0 µm constituted about 7.0%, and the largest particles, with dimensions above 30 µm, constituted about 0.9% of the volume of all the particles in the suspension, respectively. In the case of TiO2 Aeroxide® P90, a double curve of grain size distribution was observed. For the main curve, the particle size ranged from approx. 0.3 µm to approx. 18.7 µm. The particles with dimensions smaller than 1.0 µm constituted approx. 3.0% by volume of all particles in the sample. The second curve, which can be described as oversized/supersized grains, was comprised of particles ranging in size from about 21 to 170 µm, and they accounted approximately for 3.9% by volume of the total particles in the sample. The specific surface area for the samples was 0.56 m²/g for TiO2 P25 and 0.48 m²/g for TiO2 P90. It was found that the observed large particle sizes of titanium oxide particles in aqueous solutions may be the result of their agglomeration, which gives one hundred percent certainty that they will be retained by ultrafiltration and microfiltration membranes with pore sizes above 0.3 µm. [ABSTRACT FROM AUTHOR]

A laminated composite plate designed is supposed to be used under different end supports. The elastic foundation is one of such conditions. The strength of the laminated composite plates can be enhanced by altering constituents or by the addition of filler materials. For localized strengthening of laminated composite plates, such as at particular layers, it is not cost-effective to strengthen the whole structure. So, the laminated composite plates are strengthened at a particular layer by adding the fillering materials, for example, graphene or flyash. The addition of these filler materials in a particular region sometimes causes agglomeration. Agglomeration of filler materials causes adverse effects such as stress concentration or strain aging. In theoretical formulation, Eringen's nonlocal principle is applied to account for the impact of agglomeration. In the current study, neat epoxy glass laminated composite plates as well as rectangle laminated composite plate variants with outer layer graphene, core layer graphene, functionally graded laminated composite plate, laminated composite plates exclusively rich in graphene, and laminated composite plates only rich in flyash are taken into consideration. Using a layer-wise model, the fifth-order shear deformation theory is applied. The laminated composite plates are assumed to rest on an elastic foundation. The consequence of elastic coefficient of foundation on procured parameters such as fundamental frequencies, stress parameters, center deflections, and buckling performance is determined. For this purpose, computerized programs are developed using MATLAB and validated first for isotropic material. Further, the work is extended to study these effects on the laminated composite plate variants. [ABSTRACT FROM AUTHOR]

To overcome the agglomeration and insufficient combustion of nano-boron (n-B) powders, this study successfully prepared two novel types of boron-based nanocomposites using the acoustic resonance technology, namely highsubstitute nitrochitosan/nano-boron (NCh-B) with ratios of 1:3, 1:5, 1:7 and 1:9, and nitrochitosan/nano-boron powder/nano-titanium (NCh-B-Ti) with Ti contents of 5 wt%, 10 wt%, 15 wt% and 20 wt%. The structural morphologies, laser ignition and combustion properties of the composites were systematically investigated. The results suggest that the addition of NCh can significantly improve the dispersion of n-B. NCh-B exhibited a higher combustion performance than n-B, as evidenced by their ignition delay and flame areas. When the laser power density was 81 W, NCh-B5-Ti15% exhibited a combustion time and an ignition delay of 240 ms and 5.5 ms respectively, which were higher and lower than those of NCh-B5 (199 ms and 17 ms, respectively). Furthermore, NCh-B5-Ti15% displayed a lower ignition delay than both n-B powders (12 ms) and NCh-B (11 ms), as well as brighter flames and a larger combustion area. Therefore, the addition of n-Ti can promote the combustion of n-B powders, with the combustion products of NCh-B-Ti including H3BO3, B2O3, TiB2, and TiO. This study provides a new method for improving the ignition performance and combustion efficiency of n-B powders. [ABSTRACT FROM AUTHOR]

Hydrogen metallurgy is a technology that uses hydrogen instead of carbon as a reducing agent to reduce CO2 emissions. The use of hydrogen is conducive to promoting the sustainable development of the steel industry. In recent years, how to solve the sticking problem in hydrogen reduction fluidized ironmaking technology has received extensive attention. The reactor used in this paper is a fluidized bed with an inclined agitator. The effects of the agitation speed and the reduction temperature on the fluidization state of iron concentrate particles were researched by a single-factor experiment. The results depicted that adding an inclined agitator into the traditional fluidized bed can effectively reduce the sticking ratio and keep the iron concentrate particles fluidized during the reduction process. Thus, the reduction efficiency of iron concentrate particles is improved. The optimal agitation speed is 160 rpm, and the optimum reduction temperature is 1123 K. [ABSTRACT FROM AUTHOR]

Biocompatible particle-stabilized emulsions have gained significant attention in the biomedical industry. In this study, we employed dynamic high-pressure microfluidization (HPM) to prepare a biocompatible particle emulsion, which effectively enhances the thermal stability of core materials without the addition of any chemical additives. The results demonstrate that the HPM-treated particle-stabilized emulsion forms an interface membrane with high expansion and viscoelastic properties, thus preventing core material agglomeration at elevated temperatures. Furthermore, the particle concentration used for constructing the emulsion gel network significantly impacts the overall strength and stability of the material while possessing the ability to inhibit oxidation of the thermosensitive core material. This investigation explores the influence of particle concentration on the stability of particle-stabilized emulsion gels, thereby providing valuable insights for the design, improvement, and practical applications of innovative clean label emulsions, particularly in the embedding and delivery of thermosensitive core materials. [ABSTRACT FROM AUTHOR]

MXene is an emerging 2D material and shows large potential as a substrate for in situ growth of functional materials due to its merits such as large surface area, abundant nucleation sites, structural diversity, superior dispersion ability, blocking agglomeration of nanomaterials, and rich element/kind compositions. The in situ‐formed MXene‐based composites are largely applied in rechargeable batteries in the past several years by acting as active materials, serving as current collectors, decorating separators, and catalyzing electrochemical process. However, a detailed and systematic summary is still lacked. Herein, a review on in situ growth engineering on 2D MXene for next‐generation rechargeable batteries is presented in detail for the first time. Meanwhile, some outlooks and perspectives are put forward. In situ growth engineering on 2D MXenes can be achieved by calcination method, hydrothermal method, solvothermal method, room‐temperature liquid‐phase reduction method, room‐temperature liquid‐phase oxidation method, electrochemical deposition method, in situ polymerization method, vapor deposition method, mechanical milling method, microwave method, composite method, self‐reduction method, coprecipitation method, immersion method, hydrolysis method, etc. These in situ growth strategies can be extended to materials beyond MXenes, such as graphene, MBene, graphdiyne, etc. [ABSTRACT FROM AUTHOR]

A jet-based direct mixing process is used to effectively mix heterogeneous materials. In this work, its application in the structuring, coating and agglomeration of cathode materials for all-solid-state battery (ASSB) production is investigated, with the aim of increasing the homogeneity and conductivity of the composites and ultimately improving battery performance. In this process, different particle systems consisting of lithium iron phosphate (LFP), carbon black (CB) and sodium chloride (NaCl) are dispersed in the gas phase and brought together in a mixing zone as particle-laden aerosol jets. The cathode material's structure is studied through scanning electron microscopy combined with a focussed ion beam (SEM–FIB). Electrical conductivity measurements of the resulting composites assess the degree of mixing and the changes in tortuosity, while a laser light diffractor and a cascade impactor analyse the particle size distribution (PSD). The jet-based process effectively produces hetero-agglomerates with the possibility of creating different composite structures by adjusting the process parameters. The mass concentration influences not only the structure, but also the PSD in the flow and the electrical conductivity of the composite. The results serve as a basis for future experiments with solid electrolytes to comprehensively evaluate the process and the resulting battery materials. [ABSTRACT FROM AUTHOR]