Particle Surface Area Research Articles

A fully coupled solid-particle microphysics scheme for stratospheric aerosol injections within the aerosol–chemistry–climate model SOCOL-AERv2

Abstract. Recent studies have suggested that injection of solid particles such as alumina and calcite particles for stratospheric aerosol injection (SAI) instead of sulfur-based injections could reduce some of the adverse side effects of SAI such as ozone depletion and stratospheric heating. Here, we present a version of the global aerosol–chemistry–climate model SOCOL-AERv2 and the Earth system model (ESM) SOCOLv4 which incorporate a solid-particle microphysics scheme for assessment of SAI of solid particles. Microphysical interactions of the solid particle with the stratospheric sulfur cycle were interactively coupled to the heterogeneous chemistry scheme and the radiative transfer code (RTC) for the first time within an ESM. Therefore, the model allows simulation of heterogeneous chemistry at the particle surface as well as feedbacks between microphysics, chemistry, radiation and climate. We show that sulfur-based SAI results in a doubling of the stratospheric aerosol burden compared to the same mass injection rate of calcite and alumina particles with a radius of 240 nm. Most of the sulfuric acid aerosol mass resulting from SO2 injection does not need to be lifted to the stratosphere but is formed after in situ oxidation and subsequent water uptake in the stratosphere. Therefore, to achieve the same radiative forcing, larger injection rates are needed for calcite and alumina particle injection than for sulfur-based SAI. The stratospheric sulfur cycle would be significantly perturbed, with a reduction in stratospheric sulfuric acid burden by 53 %, when injecting 5 Mt yr−1 (megatons per year) of alumina or calcite particles of 240 nm radius. We show that alumina particles will acquire a sulfuric acid coating equivalent to about 10 nm thickness if the sulfuric acid is equally distributed over the whole available particle surface area in the lower stratosphere. However, due to the steep contact angle of sulfuric acid on alumina particles, the sulfuric acid coating would likely not cover the entire alumina surface, which would result in available surface for heterogeneous reactions other than the ones on sulfuric acid. When applying realistic uptake coefficients of 1.0, 10−5 and 10−4 for H2SO4, HCl and HNO3, respectively, the same scenario with injections of calcite particles results in 94 % of the particle mass remaining in the form of CaCO3. This likely keeps the optical properties of the calcite particles intact but could significantly alter the heterogeneous reactions occurring on the particle surfaces. The major process uncertainties of solid-particle SAI are (1) the solid-particle microphysics in the injection plume and degree of agglomeration of solid particles on the sub-ESM grid scale, (2) the scattering properties of the resulting agglomerates, (3) heterogeneous chemistry on the particle surface, and (4) aerosol–cloud interactions. These uncertainties can only be addressed with extensive, coordinated experimental and modelling research efforts. The model presented in this work offers a useful tool for sensitivity studies and incorporating new experimental results on SAI of solid particles.

Large eddy simulation of soot formation in a turbulent lifted flame with a discretized population balance and a reduced kinetic mechanism

This article presents simulations of a turbulent lifted flame using the large eddy simulation-transport probability density function-discretized population balance equation approach. This approach takes into account the interaction between turbulent reacting flow and soot particle formation. A reduced chemical kinetics mechanism including a series of polycyclic aromatic hydrocarbons (PAHs) species linked to soot formation is generated employing the approach of the directed relation graph error propagation and is tested on a perfectly stirred reactor under varying equivalent ratio conditions and premixed flames. The soot kinetics model includes the PAH-based nucleation and surface condensation, the hydrogen abstraction acetylene addition surface growth and oxidation mechanism, and the size-dependent aggregation. The soot morphology considers the surface area and other geometrical properties for both spherical primary particles and fractal aggregates. The simulation results show, in general, reasonably good agreement with experimental measurements in terms of lifted height, flame shape, flow-field velocity, the hydroxyl radical, and soot volume fraction. A discussion of micromixing and its modeling in the context of the Interaction by Exchange with the Mean model is also presented. To investigate the effect of the soot micromixing frequency factor on soot particles, an additional simulation is conducted where this factor is reduced by a factor of 10 for the soot particles. The maximum soot volume fraction is observed to increase slightly. However, compared with the impact of kinetics on soot modeling, this effect is a minor one.

Unveiling trends in migration of iron-based nanoparticles in saturated porous media

Nanoscale zero-valent iron (nZVI) particles are routinely used for environmental remediation, but their transport dynamics in different settings remain unclear, hindering optimization. This study introduces a novel approach to predicting nZVI transport in saturated porous model environment. The method employs advanced long column devices for real-time monitoring via controlled magnetic susceptibility measurements. Numerical modeling with a modified version of the MNMs 2023 software was then used to predict nZVI and its derivatives mobility in field-like conditions, offering insights into the radius of influence (ROI) and shape factor (SF) of their distribution. A standard nZVI precursor was compared with its four major commercial derivatives: nitrided, polyacrylic acid-coated, oxide-passivated, and sulfidated nZVI. All these iron-based nanoparticles exhibited identical particle sizes, morphologies, surface areas, and phase compositions, isolating surface properties, dominated by charge, as the sole variable affecting their mobility. The study revealed optimal transport when the surface charge of nZVI and its derivatives was strongly negative, while rapid aggregation of nZVI derivatives due magnetic attraction reduced their mobility. Modeling predictions based on column scale-up, indicated that detectable concentrations of 20 g L⁻1 were found at distances ranging from 0.4 to 1.1 m from the injection well. Slightly sulfidated nZVI traveled farther than the nZVI precursor and ensured more homogenous particle distribution around the well. Organically modified nZVI migrated the longest distances but showed particle accumulation close to the injection point. The findings suggest that minimal sulfidation combined with organic modification of nZVI surfaces may effectively enhance radial and vertical nZVI distribution in aquifers. Such improvements increase the commercial viability of modified nZVI, reduce their adverse impacts, and boosts their practical applications in real-world scenarios.

Effects of BET Surface Area and Silica Hydrophobicity on Natural Rubber Latex Foam Using the Dunlop Process

To reinforce natural rubber latex foam, fumed silica and precipitated silica are introduced into latex foam prepared using the Dunlop process as fillers. Four types of silica, including Aerosil 200 (hydrophilic fumed silica), Reolosil DM30, Aerosil R972 (hydrophobic fumed silica), and Sipernat 22S (precipitated silica), are investigated. The latex foam with added silica presents better mechanical and physical properties compared with the non-silica foam. The hydrophobic nature of the fumed silica has better dispersion in natural rubber compared to hydrophilic silica. The specific surface area of silica particles (BET) also significantly influences the properties of the latex foam, with larger specific surface areas resulting in better dispersity in the rubber matrix. It was observed that exceeding 2 phr led to difficulties in the foaming process (bulking). Furthermore, higher loading of silica also affected the rubber foam, resulting in an increased shrinkage percentage, hardness, compression set, and crosslink density. The crosslink density increased from 11.0 ± 0.2 mol/cm3 for non-silica rubber to 11.6 ± 0.6 mol/cm3 for Reolosil DM30. Reolosil DM30 also had the highest hardness, with a hardness value of 52.0 ± 2.1 IRHD, compared to 45.0 ± 1.3 IRHD for non-silica foam rubber and 48 ± 2.4 IRHD for hydrophilic fumed silica Aerosil 200. Hydrophobic fumed silica also had the highest ability to return to its original shape, with a recovery percentage of 88.0% ± 3.5% compared to the other fumed silica. Overall, hydrophobic fumed silica had better results than hydrophilic silica in both fumed and precipitated silica.

Mechanical strength analysis of bio composite made by using micro powder made of Prosopis cineraria wood

The Present study examines the mechanical strength of bio-composites fabricated from wood powder of Prosopis cineraria (Khejri) and jute fiber as reinforcement inside an epoxy resin matrix. The mechanical performance of these bio-composites was assessed by altering filler content percentages (0%, 4%, 8%, 12%, 16%, and 20%) and filler particle sizes (250 microns and 500 microns) under standard and carbonate conditions. Tensile strength and impact energy assessments were performed to evaluate the effects of filler content, particle size, and filler type on the mechanical characteristics of the composites. The tensile strength tests reveal that composites with 12% filler and a particle size of 250 microns had the maximum tensile strength, measuring 33.4 MPa under normal settings and 34.8 MPa under carbonate conditions. An increase in filler content over 12% resulted in a reduction in mechanical strength due to filler agglomeration, which decreased stress transfer efficiency. The composites with 250-micron particles consistently demonstrated superior tensile and impact strengths compared to those with 500-micron particles, due to the increased surface area of the smaller particles. Comparative analysis of normal and carbonate conditions demonstrated that carbonate fillers offered superior reinforcement owing to their increased density and enhanced matrix-filler interaction, leading to augmented tensile and impact strength. These findings provide significant insights into the development of bio-composites for structural applications, namely in improving their mechanical strength and durability.

New Insights on the Burst Release Kinetics of Spray-Dried PLGA Microspheres.

Spray drying is one of the leading manufacturing methods for active pharmaceutical ingredients (APIs) owing to its rapid, single-step, and cost-effective nature. It also has the capacity to generate microspheres capable of controlled release of APIs including biomolecules and vaccines. However, one of the key challenges of spray-dried formulations especially with poly(lactic-co-glycolic acid) (PLGA)-based controlled-release injectables is burst release, where a significant fraction of the API is released prematurely within a short period of time following administration, leading to detrimental impact on the performance and quality of end products. This study uses a model API, bovine serum albumin (BSA) protein, to identify the sources of burst release that may affect the kinetics and performance of long-acting injectable microsphere formulations. Spray-dried microspheres with various formulations (i.e., variable BSA/PLGA ratios) were characterized in terms of their morphology, particle size, surface area, thermal properties, moisture content, as well as chemical compositions and their distributions to investigate the impact of spray drying on the burst release phenomenon. The results suggest that a relatively high initial release (85%) observed is mainly attributed to the protein distribution close to the particle surface. Morphology analysis provided evidence that the microspheres retained their spherical structure during the burst release phase. X-ray photoelectron spectroscopy, hard X-ray photoelectron spectroscopy, and argon cluster sputtering-assisted time-of-flight secondary ion mass spectrometry analysis suggest an enrichment of PLGA on particle surfaces with buried BSA protein. The statistically significant difference in particle size and surface area between three different formulations may be responsible for an initial variation in release but did not seem to alter the overall burst release profile. Considering the suggested source of burst release, the two-fluid spray-drying method, characterized by a single liquid feed delivering a preprepared emulsion, generated matrix-type microspheres with a surface layer of PLGA, as evidenced by surface analysis. The PLGA surface layer proved to be prone to degradation and pore formation, allowing for faster diffusion of BSA out of the microspheres, resulting in a burst release. Increasing the polymer concentration did not seem to halt this process.

Investigation on preparation and properties of gel type 188W/188Re generator

As one of the most important integrated nuclides for diagnosis and treatment in recent years, rhenium-188 (188Re) has a broad scope in the clinical application. Due to the specific properties of such radionuclide, it was mainly provided by the chromatographic 188W-188Re generators. There is no doubt that the application of 188Re in the treatment of various diseases depended on the development of 188W-188Re generator. Considering the high standards of such technology on radioactive activity of 188W and impurity content, a 188W-188Re generator filled with the zirconium tungstate gel has been prepared in this work. The effects of molar ratio of chemical agents, pH, reaction temperature, drying methods, rinsing methods and other conditions on the synthesis of gel particles have been studied. Furthermore, a variety of characterization techniques were used to observe the macro-/micro-morphology and chemical structure of gel particles. It can be concluded that vacuum freeze-dried method could significantly increase the specific surface area, pore size and tungsten content of gel particle. In order to decrease the content of 188W in the elute, a handful of acidic alumina was filled in the bottom of our 188W-188Re generator, an elution and purification integrated-generator was formed. During the first five processes, the nuclear purity of 188Re solution was above 99.99%, the radiochemical purity was approximately 99.5%, the pH value was 5.0–7.0 and the average elution efficiency reached up to 82.7%. In addition, the leakage rate of 188W was low as 1.60 × 10−6, and the peak of elute curve was located at 2 mL without the trailing phenomenon. This work lays a solid foundation for the domestic demand of daughter nuclide 188Re, further makes an outstanding contribution to the application of the radiation therapy technology and the protection of people's health.

Effects of nitrogen vacancy sites of oxynitride support on the catalytic activity for ammonia decomposition

Nitrogen-containing compounds such as imides and amides have been reported as efficient materials that promote ammonia decomposition over nonnoble metal catalysts. However, these compounds decompose in an air atmosphere and become inactive, which leads to difficulty in handling. Here, we focused on perovskite oxynitrides as air-stable and efficient supports for ammonia decomposition catalysts. Ni-loaded oxynitrides exhibited 2.5–18 times greater catalytic activity than did the corresponding oxide-supported Ni catalysts, even without noticeable differences in the Ni particle size and surface area of the supports. The catalytic performance of the Ni-loaded oxynitrides is well correlated with the nitrogen desorption temperature during N2 temperature-programmed desorption, which suggests that the lattice nitrogen in the oxynitride support rather than the Ni surface is the active site for ammonia decomposition. Furthermore, NH3 temperature-programmed surface reactions and density functional theory (DFT) calculations revealed that NH3 molecules are preferentially adsorbed on the nitrogen vacancy sites on the support surface rather than on the Ni surface. Thus, the ammonia decomposition reaction is facilitated by a vacancy-mediated reaction mechanism.

Particle tracking-aided digital volume correlation for clay–sand soil mixtures

In this study, a novel, interdisciplinary method is introduced that merges fundamental geomechanics with computer vision to develop an advanced hybrid feature-aided digital volume correlation (DVC) technique. This technique is specifically engineered to measure and compute the full-field strain distribution in fine-grained soil mixtures. A clay–sand mixture specimen composed of quartz sand particles and kaolinite was created. Its mechanical properties and deformation behaviour were then tested using a mini-triaxial apparatus, combined with micro-focus X-ray computed tomography (μCT). The CT slices underwent image processing for denoising, segmentation of distinct phases, reconstruction of sand particles and feature extraction within the soil specimen. The proposed approach incorporated a two-step particle tracking method, which initially uses particle volume and surface area features to establish a preliminary matching list for a reference particle and then use the iterative closest point method for precise target particle matching. The soil specimen's initial displacement field was then mapped onto the DVC method's grid, and further refined through sub-voxel registration by way of a three-dimensional inverse compositional Gauss–Newton algorithm. The proposed method's effectiveness and efficiency were validated by accurately calculating the displacement and strain fields of the soil mixture sample, and comparing the results with those from a traditional DVC method. Given the soil's compositional and microstructural characteristics, these image-matching techniques can be integrated to create a versatile, efficient, and robust DVC system, suitable for a variety of soil mixture types.

Silica surface modification using cellulose as a renewable organosilane derived from coconut coir fiber for carbon capture

The properties of silica surface modification for carbon capture were studied, utilizing cellulose-amine as a modification agent derived from dissolved coconut coir fiber. To form bonds with NH2 functional groups through amination processes, cellulosic biomass waste is utilized, which is analogous to replacing alkoxy ligands. The dual-function mixture reagents dimethyl sulfoxide (DMSO) and ammonium hydroxide (NH4OH) were employed in the same system as the amine sources and solvents. Waterglass is used as a source of silica, and the modified particles are formed using a one-step consecutive sol-gel spray drying process used in a direct condensation route. Changes in the concentration of sodium lauryl sulfate (SLS) were examined to determine how they affected the essential parameters of the particles. The template is removed during particle formation without further physical or chemical processing. The particle morphology changed from donut-shaped to spherical after SLS application, as evidenced by the increase in SLS concentration. This also shows that the increase in the particle surface area is directly influenced by the increase in the formation of new pore structures with increasing SLS concentration. Through this mechanism, it is possible to extend the pore size distribution to the meso-macropore regime and initiate the formation of new mesopores. This has a direct impact on the capacity to absorb CO2 gas by increasing the cellulose-amine mass fraction that can be grafted to as high as 32.35 %wt. At an operating pressure of 6 bar, a maximum CO2 gas adsorption capacity of 5.32 mmol/g silica was attained by adding SLS 3 CMC to the silica particles. This value is 2.3 times higher than that obtained when using an aminosilane-based modification agent.

Effects of Size and Mechanical Pre-Treatment on Aluminium Recovery from Municipal Solid Waste Incineration Bottom Ash

Municipal solid waste (MSW) is incinerated to reduce the volume and recover energy and materials. The generation of MSW has been increasing over the past few decades due to the increase in population and changing consumption habits. Rising environmental and economic concerns have increased the importance of waste treatment and recovery. Currently, MSW may take three alternate or parallel routes: direct recycling, incineration, or landfill, depending on the country and location. MSW incineration has three products in addition to energy: bottom ash, fly ash, and off-gas. After incineration, bottom ash usually still contains many materials to be recovered, such as glass, ceramics, and metals with a degree of oxidation. This study focuses on aluminium recovery from MSW incineration bottom ash from two different countries. The 2–30 mm fraction of aluminium particles was characterized in terms of its size, shape, and oxide thickness, and its effects on aluminium recovery were investigated. In addition, the ability of mechanical pre-treatment to remove oxides prior to melting was studied. The results were compared with the analytical modeling developed in this study. An increasing particle size and surface area resulted in an increase in aluminium recovery. Mechanical pre-treatment increased the yield for smaller particles to a larger extent than larger particles due to the difference in the oxide/metal ratio.

CeO2 enhanced performance of NiFe2O4-CaO for carbon capture and in-situ hydrogenation conversion to CO

NiFe2O4 exhibits excellent redox properties and is widely applied in CaO-NiFe2O4 chemical looping processes. However, rapid sintering of Ni-Fe alloy under reaction conditions limited its industrial applications. The CeO2-NiFe-CaO were synthesized through a physical mixing method with NiFe2O4 as a precursor, and its CO2 capture capacity and in-situ hydrogenation performance were conducted on ICCC-RWGS reaction under different conditions. 20CeO2-NiFe-CaO exhibited a CO yielding of 9.35 mmol/g at 650 °C. During the carbon capture stage, CO2 was adsorbed by CaO, leading to the formation of CaCO3. In the hydrogenation conversion stage, hydroxyl groups were generated on the surface, combining with CaCO3 to produce formate species, further generating H2O and CO. 15CNF-CaO exhibited superior cyclic ICCC-RWGS reaction performance compared to 15NF-CaO, with a CO yield of 1.88 mmol/g after 40 cycles. CeO2 inhibited the sintering of catalytic components, preserving a higher specific surface area and smaller particle size. Furthermore, CeO2 in 15CNF-CaO inhibited carbon deposition and enhanced in-situ hydrogenation performance, exhibiting better CaO regeneration capability and better cyclic stability. These results could provide insight for designing the DFMs for the ICCC-RWGS process.

Enhanced drug release through nitrendipine/hydroxypropyl methylcellulose solid dispersion via supercritical antisolvent technique

The poor water solubility of nitrendipine (NT) results in low oral bioavailability, which hinders its practical application. Hydroxypropyl methylcellulose (HPMC) is a prominent drug carrier that has been applied in the biomedical field due to its significant characteristics, such as large surface area, biocompatibility and biodegradability. In this study, an efficient drug delivery system based on the preparation of NT/HPMC solid dispersion using supercritical antisolvent (SAS) technology was proposed. The effect of different operating parameters such as solvent, host guest ratio, concentration, temperature, and pressure on NT/HPMC was optimized to obtain dispersed particles with maximum solubility. The formed solid dispersion presents non-static spherical particles with a high surface area and small particle size. Importantly, in vitro drug release studies have demonstrated that the dissolution and solubility of NT in solid dispersion are significantly enhanced compared to pure drug. In vitro bioactivity experiments showed that the NT/HPMC solid dispersion has good biocompatibility and antibacterial performance. Thus, this study indicates that solid dispersion prepared using SAS technology are considered a promising drug delivery system.

Enhancing chemical heat storage performance of nanocarbon porous particle based MgO/Mg(OH)2 composite by calcination method

The application of MgO/Mg(OH)2 in heat storage technology has been limited due to slow hydration rate and easy agglomeration. In this paper, nanoporous carbon particle (NCP) as a carrier was used to prepare NCP/MgO chemical heat storage composite materials by impregnation and calcination methods, respectively. The microstructure characterization, hydration reaction, and simultaneous thermogravimetric analysis experiments were carried out on the prepared composite materials. The results showed that the internal distribution of MgO in the composite material prepared by calcination method was more uniform, and the particle size of MgO was smaller. Under the conditions of 110 ℃ hydration temperature and 57.8 kPa water vapor partial pressure, the hydration conversion ratio of the composite material prepared by calcination method after 120 min of hydration conversion ratio reached 93 %, which was 17.7 % higher than that of the impregnated composite material and 50 % higher than that of pure MgO. Under the comprehensive influence of specific surface area, pore structure, and active component particle size, compared with pure materials and impregnated composite materials, the dehydration rate of the composite material prepared by calcination method at 300 ℃ was twice that of impregnated method and 6 times that of pure MgO, and the heat storage density reached 1039kJ/kg. After 10 cycles, the heat storage density still maintained an initial state of 95.8 %. Compared with pure materials and impregnated composite materials, NCP/MgO composite materials prepared by calcination method had better heat storage performance and higher cyclic stability.

Systematic screening of particle engineered polymers for the preparation of multiparticulates embedded orally disintegrating tablets

This paper evaluated polymers' physical and mechanical properties to formulate modified-release multiparticulates to be embedded in orally disintegrating tablets (ODTs). The targeted polymer should have adequate elastic-plastic properties in a multiparticulate system during the manufacturing process, which is affected by its physical properties. The good mechanical properties of the multiparticulate system can effectively aid in retaining the shape of the particles from being affected under applied compression pressure during the formulation process and tablets preparations. Therefore, the formulation should have good mechanical attains. Five polymers (three natural and two synthetic), namely: sodium alginate, polyvinyl alcohol (PVA), methylcellulose (MC), polyacrylic acid (PAA) and Eudragit L100, were evaluated. Polymers in raw form or particle engineered using spray drying were characterised using different analysis techniques: differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), compacts tensile strength, texture analysis, particle size analysis and surface area analysis. The unprocessed PAA exhibited the lowest Young's modulus, measuring at 5.38 MPa, whereas MC displayed the highest value of 14.74 MPa. The polymers were subjected to spray drying at a concentration of 5% w/v. Data of the texture analysis revealed that Young's modulus increased for the spray-dried PAA powder, reaching 13.69 MPa. This suggests an enhanced polymer compressibility subsequent to the spray drying process. Eudragit L100 demonstrated an enhanced tabletability prolife after spray drying. SEM and surface area results showed a correlation with the mechanical findings. Plasticity and elasticity together provide strong, durable tablets with structural integrity. Achieving a balance between these properties is crucial for effective tabletability. The results of this study provide an insight into physical and mechanical properties and changes encountered upon spray drying. A balance between elastic- plastic properties is required for optimal multiparticulate development.

Non-steady flow decomposition behaviors of heat and mass transfer on intrinsic kinetics for methane hydrate particles transported in pipelines

The differential equations governing the decomposition rate and activation energy, convective mass transfer, methane diffusion and fugacity, as well as heat conduction and enthalpy change were derived by integrating thermal convection, heat conduction, mass transfer and intrinsic kinetics. Mathematical models for decomposition kinetics and thermodynamics in a non-steady field were solved using a radial logarithmic grid for node division and discretization of the equations. The study elucidated the heat and mass transfer processes as well as decomposition kinetics in pipelines by analyzing the impacts of particle size, temperature, pressure, flow rate and activation energy on decomposition rate. The results indicated that compared with the isothermal decomposition of the intrinsic kinetic model and static experimental decomposition, the complex non-steady multiphase flow model offers a more accurately simulation of hydrate decomposition as well as associated heat and mass transfer processes. Hydrate decomposition is characterized as a non-isothermal dynamic ablation process with heat transfer rate and intrinsic kinetics dominating during the preliminary stage and the stable stage, respectively. An increasing in the slurry temperature, temperature fluctuation and flow rate accelerated the heat transfer rate capacity, enhanced convective heat transfer capacity and facilitated hydrate decomposition, with the mass transfer rate exhibiting lesser influence. The particle surface area and slurry temperature exhibited the most significant influence on hydrate decomposition, which was followed by flow rate. Upon increasing particle size from 1 mm to 5 mm and the temperature from 293 K to 313 K, the decomposition rate increased by 20.7 times and 13.5 times, respectively. Furthermore, enhancing temperature and flow rate while decreasing particle size and pressure decreased both the decomposition time and the duration required for the decomposition rate to reach its peak. Additionally, the decomposition rate and its constant vary with the activation energy.

Single-Particle Crushing Test of Coated Calcareous Sand Based on MICP

Calcareous sand is a crucial construction material for island and reef development and reinforcing it using Microbially Induced Calcite Precipitation (MICP) technology is a promising new method. This study employed 3D scanning technology to assess changes in the particle size and morphology of MICP-treated, coated calcareous sand particles. Single-particle crushing tests were conducted to analyze their crushing strength, crushing energy, crushing modes, and fragment fractal dimensions. The results indicated that MICP treatment significantly increased particle size, surface area, and volume, while reducing flatness. At a cementation solution concentration of 1 mol/L, both crushing strength and crushing energy were optimized. The coated particles exhibited three crushing modes: explosive crushing, mixed crushing, and splitting crushing. Thicker coatings led to a tendency for particles to break into larger fragments through the mixed and splitting crushing modes. Fractal analysis revealed that coating thickness directly affects the local crushing characteristics of the particles.

Valorization of coffee cherry waste ash as a sustainable construction material

This study explores the potential of treated coffee cherry waste (T-CCW) as a partial replacement of cement in mortar. T-CCW was characterized and incorporated into pastes and mortars at 5 %–25 % cement replacement. The main objectives were to examine the fresh and hardened properties, hydration, and environmental assessment. Results showed that the high specific surface area and porous structure of T-CCW particles increased water demand and accelerated setting times. T-CCW incorporation of up to 15 % enhanced compressive strength at all curing ages due to improved hydration and limited pozzolanic reactions. Ultrasonic pulse velocity indicated good homogeneity and compactness in T-CCW blended mortars. Microstructural analysis revealed that T-CCW enhanced cement hydration, leading to a denser matrix. Environmental analysis showed a reduced embodied carbon and cement intensity index compared to the control mix. Overall, the optimal performance was observed at 15 % T-CCW replacement, significantly improving engineering properties and environmental impact. Further, the fishbone diagram addresses various factors to optimize the use of T-CCW as a cementitious composite. These findings demonstrate the potential of T-CCW as a sustainable construction material, offering a promising pathway towards environmentally friendly and resource-efficient building practices while addressing waste management in the coffee industry.

The effect of carbon addition on the synthesis process and the physical/electrocatalytic properties of FeTiO3 nanopowder produced by solution combustion synthesis method

The FeTiO3 nanopowder is a vital engineering material known for its exceptional performance in energy generation, storage, electrochemical sensors, and catalysis. However, synthesizing FeTiO3 nanopowder with high crystallinity and phase purity typically requires specialized equipment and controlled heat treatment due to the instability of Fe2+ ions. Using the one-step solution combustion synthesis (SCS) method, FeTiO3 nanopowder withe high crystallinity were successfully produced utilizing basic equipment. Additionally, the influence of carbon additives on phase transitions, as well as the physical and physicochemical properties of the synthesized powder, was examined. XRD results indicate that increasing the amount of fuel, particularly glycine, creates a stable environment for the crystallization of FeTiO3 nanoparticles. Moreover, enhancing the carbon content in precursor solutions with urea enhances reduction conditions and boosts the stability of FeTiO3 in the final product. The presence of carbon additives in glycine-fuel samples leads to unfavorable outcomes by increasing the levels of TiO2 and Fe3O4 undesirable phases. Incorporating additive carbon into the urea-synthesized precursor solution resulted in a particle size increase exceeding 50 nm and raised the combustion temperature by a minimum of 230 °C. Furthermore, the presence of 15 wt% additive carbon in the sample synthesized with glycine improved the specific surface area of particles from 2.44 m2/g to 18.41 m2/g. Obtained results have shown that achieving high crystallinity of FeTiO3 nanopowder is feasible through a one-step solution combustion synthesis process. This can be accomplished by carefully choosing the synthesis conditions, such as the type and quantity of fuel, along with the carbon additive.

Absorption of commercial and nanoparticulate ZnO and MgO synthesized by combustion reaction applied to maize soil

Nanotechnology has rapidly expanded across various fields, yet its application in agriculture remains underexplored. This study investigates the impact of zinc oxide (ZnO) and magnesium oxide (MgO) nanoparticles on maize cultivation, comparing commercial samples with those synthesized by combustion reaction. Synthesized ZnO and ZnO/MgO (1:1 by mass) were characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) to determine particle size and morphology. The experimental design assessed the effects of different treatments on magnesium and zinc uptake in maize roots and leaves, using atomic absorption spectrometry (AAS) for analysis. Results indicate that commercial ZnO significantly increased Zn absorption compared to synthesized samples and the control group, highlighting the influence of particle size and surface area on nutrient uptake. This study provides valuable insights into the potential of nanomaterials into the plant’s absorption mechanism as well as show that the availability of Zn NP synthesized contributes to the absorption of zinc by the plant without competing with Mg. On the other hand, when in Zn commercial, Mg absorption may be impaired.