Particle Surface Research Articles

Quality assessment standards and production technology of artificial sand based on hydraulic concrete construction specifications

Natural sand and gravel resources are a local resource. Natural sand and gravel are non-renewable in a short time and are not suitable for long-distance transportation. After decades of mining, sand and gravel resources in some areas have been exhausted. The transportation distance of natural sand and gravel is getting farther and farther, and accordingly, the price of natural sand and gravel continues to rise. At the same time, continuous and disorderly mining has caused serious damage to the environment and resources. During the construction of large and medium-sized water conservancy and hydropower projects in China, due to the lack of surrounding natural aggregates, most projects use artificial aggregates. In the current national standards for water conservancy projects, the content of artificial sand and gravel powder is clearly defined. Based on the “Hydraulic Concrete Construction Specifications” (SL677-2014), this article summarizes the particle shape, gradation and surface structure of artificial sand, and also calculates the theoretical gradation of artificial sand. To find out the impact of stone powder content on the performance of artificial sand, different levels of stone powder content need to be selected for research and analysis to clarify the impact of artificial sand powder content on concrete properties. Research shows that for concrete made from artificial sand, increasing the aggregate content with a particle size less than 0.075 mm can significantly increase the compressive strength of the concrete. In artificial sand, the content of stone powder will affect the workability, polishability, durability, permeability and water release of concrete. In the artificial sand and gravel production process system, crushing and sand making equipment are the most important sand and gravel production equipment. The research results provide theoretical reference for the application of artificial sand in concrete and the update of artificial sand production technology and equipment.

Suppression of Segmental Chain Dynamics on a Particle's Surface in Well-Dispersed Polymer Nanocomposites.

The Rouse dynamics of polymer chains in model nanocomposite polyethylene oxide/silica nanoparticles (NPs) was investigated using quasielastic neutron scattering. The apparent Rouse rate of the polymer chains decreases as the particle loading increases. However, there is no evidence of an immobile segment population on the probed time scale of tens of ps. The slowing down of the dynamics is interpreted in terms of modified Rouse models for the chains in the NP interphase region. Thus, two chain populations, one bulk-like and the other characterized by a suppression of Rouse modes, are identified. The spatial extent of the interphase region is estimated to be about twice the adsorbed layer thickness, or ≈2 nm. These findings provide a detailed description of the suppression of the chain dynamics on the surface of NPs. These results are relevant insights on surface effects and confinement and provide a foundation for the understanding of the rheological properties of polymer nanocomposites with well-dispersed NPs.

Formulation of geopolymer binder based on volcanic-scoria and clay brick wastes using rice husk ash-NaOH activator: Fresh and hardened properties

The present study investigated the influence of the replacement of waste clay bricks (WB) by volcanic scoria (Zg) on the fresh and hardened properties of geopolymer binders for potential construction applications at ambient temperature. Geopolymer paste samples were prepared using Zg as raw material blended with WB ranging from 0 to 50 wt% of total raw materials. Alternative alkaline activator used for the geopolymer synthesis was prepared by mixing rice husk ash (RHA) and 6 mol/L of NaOH solution. The geopolymers were cured at room temperature for 28 days, then subjected to mechanical property tests; microstructural and macrostructural characterization studies. Results showed that both flowability and setting time of geopolymer mixtures decreased with increases in WB content. The reduction in workability could be attributed to increase in the relatively rough surface of WB particles, which resulted in inter-particle friction. Flexural strength increased from 4 to 12 MPa while the compressive strength 24–52 MPa with the increase in WB up to 50%. The WB powders enriched Al content in mixtures, establishing the Si-O-Al bonds, confirmed by 27Al MAS NMR spectroscopy exhibiting the more Al(IV) sites integrating the N-A-S-H network. Incorporating the WB powders contributed to the development of densified matrix.

Observation-constrained kinetic modeling of isoprene SOA formation in the atmosphere

Abstract. Isoprene has the largest global non-methane hydrocarbon emission, and the oxidation of isoprene plays a crucial role in the formation of secondary organic aerosol (SOA). Two primary processes are known to contribute to SOA formation from isoprene oxidation: (1) the reactive uptake of isoprene-derived epoxides on acidic or aqueous particle surfaces and (2) the absorptive gas–particle partitioning of low-volatility oxidation products. In this study, we developed a new multiphase condensed isoprene oxidation mechanism that includes these processes with key molecular intermediates and products. The new mechanism was applied to simulate isoprene gas-phase oxidation products and SOA formation from previously published chamber experiments under a variety of conditions and atmospheric observations during the Southern Oxidant and Aerosol Studies (SOAS) field campaign. Our results show that SOA formation from most of the chamber experiments is reasonably reproduced using our mechanism, except when the concentration ratios of initial nitric oxide to isoprene exceed ∼ 2, the formed SOA is significantly underpredicted. The SOAS simulations also reasonably agree with the measurements regarding the diurnal pattern and concentrations of different product categories, while the total isoprene SOA remains underestimated. The molecular compositions of the modeled SOA indicate that multifunctional low-volatility products contribute to isoprene SOA more significantly than previously thought, with a median mass contribution of ∼ 57 % to the total modeled isoprene SOA. However, this contribution is intricately intertwined with IEPOX-derived SOA (IEPOX: isoprene-derived epoxydiols), posing challenges for their differentiation using bulk aerosol composition analysis (e.g., the aerosol mass spectrometer with positive matrix factorization). Furthermore, the SOA from these pathways may vary greatly, mainly dependent on the volatility estimation and treatment of particle-phase processes (i.e., photolysis and hydrolysis). Our findings emphasize that the various pathways to produce these low-volatility species should be considered in models to more accurately predict isoprene SOA formation. The new condensed isoprene chemical mechanism can be further incorporated into regional-scale air quality models, such as the Community Multiscale Air Quality Modelling System (CMAQ), to assess isoprene SOA formation on a larger scale.

Engineering a Rigid Nucleic Acid Structure to Improve the Limit of Detection for Genetic Assays.

Detecting nucleic acids at ultralow concentrations is critical for research and clinical applications. Particle-based assays are commonly used to detect nucleic acids. However, DNA hybridization on particle surfaces is inefficient due to the instability of tethered sequences, which negatively influences the assay's detection sensitivity. Here, we report a method to stabilize sequences on particle surfaces using a double-stranded linker at the 5' end of the tethered sequence. We termed this method Rigid Double Stranded Genomic Linkers for Improved DNA Analysis (RIGID-DNA). Our method led to a 3- and 100-fold improvement of the assays' clinical and analytical sensitivity, respectively. Our approach can enhance the hybridization efficiency of particle-based assays without altering existing assay workflows. This approach can be adapted to other platforms and surfaces to enhance the detection sensitivity.

Mechanically suitable and osteoinductive 3D-printed composite scaffolds with hydroxyapatite nanoparticles having diverse morphologies for bone tissue engineering.

The challenge of integrating hydroxyapatite nanoparticles (nHAp) with polymers is hindered by the conflict between the hydrophilic and hygroscopic properties of nHAp and the hydrophobic properties of polymers. This conflict particularly affects the materials when calcium phosphates, including nHAp, are used as a filler in composites in thermal processing applications such as 3D printing with fused filament fabrication (FFF). To overcome this, we propose a one-step surface modification of nHAp with calcium stearate monolayer. Moreover, to build the scaffold with suitable mechanical strength, we tested the addition of nHAp with diverse morphology-spherical, plate- and rod-like nanoparticles. Our analysis showed that the composite of polycaprolactone (PCL) reinforced with nHAp with rod and plate morphologies modified with calcium stearate monolayer exhibited a significant increase in compressive strength. However, composites with spherical nHAp added to PCL showed a significant reduction in compressive modulus and compressive strength, but both parameters were within the applicability range of hard tissue scaffolds. None of the tested composite scaffolds showed cytotoxicity in L929 murine fibroblasts or MG-63 human osteoblast-like cells, supporting the proliferation of the latter. Additionally, PCL/nHAp scaffolds reinforced with spherical nHAp caused osteoactivation of bone marrow human mesenchymal stem cells, as indicated by alkaline phosphatase activity and COL1, RUNX2, and BGLAP expression. These results suggest that the calcium stearate monolayer on the surface of the nHAp particles allows the production of polymer/nHAp composites suitable for hard tissue engineering and personalized implant production in 3D printing using the FFF technique.

A Macroscopic Interpretation of the Correlation between Electrical Percolation and Mechanical Properties of Poly-(Ethylene Vinyl Acetate)/Zn Composites

Elastic composites were prepared using a procedure involving hot plates and zinc powder that was directly dispersed into an EVA matrix. The correlation between the zinc content and the conductive properties of the material was studied via impedance spectroscopy, the thermal properties of the material were studied via differential calorimetry and the mechanical properties of the composites were studied via tensile strength curves, representing an important advancement in the characterization of this type of composite material. The composites’ tensile strength and elongation at break decrease with the addition of filler since zinc particles act as stress-concentrating centres, while the composites’ hardness and Young’s modulus increase because of an increase in the stiffness of the material. The AC perturbation across the EVA/Zn composites was characterized using an RC parallel equivalent circuit that allowed us to easily measure their resistivity (ρp) and permittivity (εp). The dependence of these electrical magnitudes on the zinc content is correlated with their mechanical properties across the characteristic time constant τp = ρp·εp of this equivalent circuit. The dependence of the mechanical and electrical magnitudes on the zinc content is consistent with the formation of percolation clusters. The addition of graphite particles increases their potential performance. Three possible mechanisms for the electrical transport of the ac-perturbation across the EVA/Zn composites have been identified. Chemical corrosion in acid media causes the loss of zinc surface particles, but their bulk physical properties practically remain constant.

Estimation of the earlywood and latewood ratio with different particle size of dry and wet milled Japanese cedar wood flour by using hyperspectral imaging

Mechanical properties of wood–plastic composites are influenced by a particle size and surface morphology of wood flour. Generally various sizes of wood flour are produced from single solid wood even if the single process is used. If the different particle size of wood flour is produced from different wood tissue such as earlywood (EW) and latewood (LW), not only particle size but also density and chemical composition of wood flour might influence the mechanical property of final products. This study aims to investigate the relationship between particle size and their origin; EW and LW. EW and LW were separately milled to produce the EW and LW flour by dry and wet milling. Hyperspectral images ranging 400–1000 nm for each wood flour were used as training data. Discriminant model of EW and LW flour developed by PLS-DA showed over 0.77 of accuracy. Then the EW and LW were dry and wet milled together and screened by three different sieve openings to obtain different particle size wood flour. Discriminant model was applied for the hyperspectral images of each size of wood flour to estimate the EW and LW ratio. The result showed that increasing sieve opening resulted in the increasing ratio of LW for dry milled wood flours. The results suggest that the EW was easily pulverized than LW.

Research Strategies for Precise Manipulation of Micro/Nanoparticle Drug Delivery Systems Using Microfluidic Technology: A Review

AbstractMicrofluidic technology facilitates precise control over fluid mixing and interactions between the components, including self-assembly and precipitation. It offers new options for accurately manufacturing particles and holds significant potential in advancing micro/nanoparticle drug delivery systems (DDSs). Various microchannel/microfluidic chips have been explored to construct micro/nanoparticle DDSs. The precise manipulation of particle size, morphology, structure, stiffness, surface characteristics, and elasticity through microfluidic technology relies on specific microchannel geometrical designs and the application of exogenous energy, adhering to the principles of fluid motion. Consequently, this enables reproducible control over critical quality attributes (CQAs), such as particle size and distribution, encapsulation efficiency, drug loading, in vitro and in vivo drug delivery profiles, Zeta potential, and targeting capabilities, for micro/nanoparticle DDSs. In this review, we categorize microfluidic techniques and explore recent research developments in novel microchannel structures spanning the past 5 years (2018–2023) and their applications in micro/nanoparticle DDSs. Additionally, we elucidate the latest manipulation strategies of microfluidic techniques that impact foundational structures related to the CQAs of micro/nanoparticle DDSs. Furthermore, we offer insights into the industrial applications and challenges microfluidic techniques face in the context of novel micro/nanoparticle DDSs.

Internal Force Mechanism of Pisha Sandstone as a Soil Amendment to Improve Sandy Soil Structural Stability in Mu Us Sandy Land

Compounding Pisha sandstone (PSS) with sandy soil in Mu Us Sandy Land is a viable agronomical measure to effectively reduce soil erosion and improve soil quality due to the complementary characters and structures of the two materials. Aggregate stability is an important indicator to assess sandy soil erosion resistance and quality, which could be largely affected by soil surface electrochemical properties and particle interaction forces. However, the effect of the compound ratio and particle interaction forces on the aggregate stability of compound soils with Pisha sandstone and sandy soil is still unclear. Therefore, in this study, the electrochemical properties, particle interaction forces, and their effects on the aggregate stability of PSS and sandy soil at five volume ratios (0:1, 1:5, 1:2, 1:1, and 1:0) were determined to clarify the internal force mechanism of PSS to increase sandy soil structural stability in a 10-year field experiment. Experiments were measured by a combined method for the determination of surface properties and aggregate water stability. A ten-year field study revealed that the incorporation of Pisha sandstone significantly enhanced the soil organic carbon (SOC) and cation exchange capacity (CEC) (p < 0.05), while the CEC value notably increased from 4.68 to 13.76 cmol·kg−1 (p < 0.05). The soil surface potential (absolute value) and the electric field intensity gradually decreased with the increase in the Pisha sandstone content. For the compound soil particle interaction force, the addition of Pisha sandstone enhanced the van der Waals attraction force, reduced the net repulsive force between compound soil particles, and promoted the agglomeration of aeolian sandy soil. The overall trend of the aggregate breaking strength of compound soils under different addition ratios of PSS was 1:0 > 1:1 > 0:1 > 1:5 > 1:2. When the Pisha sandstone content in the compound soils was <50%, the aggregate stability was mainly influenced by compound soil particle interaction forces, and the interaction force increase was the key reason for the aggregate breakdown. When the Pisha sandstone content in the compound soils was ≥50%, the aggregate stability was affected by the combined effects of the compound soil particle composition and particle interaction forces. These results indicate that PSS addition ratios and particle interaction force are important factors affecting the structural stability of compound soils, in which the volume ratio of PSS to sandy soil of 1:2 is the appropriate ratio. Our study provides some theoretical references for further understanding of the compound soil structure improvement and sandy soil erosion control in Mu Us Sandy Land.

Composition-dependent morphologies of CeO2 nanoparticles in the presence of Co-adsorbed H2O and CO2: a density functional theory study.

Catalytic activity is affected by surface morphology, and specific surfaces display greater activity than others. A key challenge is to define synthetic strategies to enhance the expression of more active surfaces and to maintain their stability during the lifespan of the catalyst. In this work, we outline an ab initio approach, based on density functional theory, to predict surface composition and particle morphology as a function of environmental conditions, and we apply this to CeO2 nanoparticles in the presence of co-adsorbed H2O and CO2 as an industrially relevant test case. We find that dissociative adsorption of both molecules is generally the most favourable, and that the presence of H2O can stabilise co-adsorbed CO2. We show that changes in adsorption strength with temperature and adsorbate partial pressure lead to significant changes in surface stability, and in particular that co-adsorption of H2O and CO2 stabilizes the {100} and {110} surfaces over the {111} surface. Based on the changes in surface free energy induced by the adsorbed species, we predict that cuboidal nanoparticles are favoured in the presence of co-adsorbed H2O and CO2, suggesting that cuboidal particles should experience a lower thermodynamic driving force to reconstruct and thus be more stable as catalysts for processes involving these species.

Effect of particle size on optical and electrical properties of thin films – a simulation approach

This paper presents a simulated investigation of the relationship between surface roughness and particle size as well as the resulting impact of the both on the thin film’s physical and optical properties. Non-porous thin films are created through computer simulation for a range of particle sizes following the random deposition with a surface relaxation approach. For the deposited thin films different fundamental parameters like transmittance, reflectance, absorption coefficients, frequency dependent dielectric constants, loss angle, refractive indices, optical band gap have all been calculated and in this process of calculation the fundamental values of two different materials; zinc oxide (ZnO and cadmium selenide (CdSe) are taken. It has been seen that when the particle sizes are comparable the calculated values of optical band gap of both ZnO and CdSe matches well with the experimental values of the same reported by others. This is probably the first effort to develop a direct relation between the particle size with different fundamental optical properties of different materials through simple simulation which agrees well with the experimental result. This would definitely help the experimental researchers in the field of material science to design their experiments as per the desired requirements.

Near-Unity Photoluminescence Quantum Yield of Core-Only InP Quantum Dots via a Simple Postsynthetic InF3 Treatment.

Indium phosphide (InP) quantum dots (QDs) are considered the most promising alternative for Cd and Pb-based QDs for lighting and display applications. However, while core-only QDs of CdSe and CdTe have been prepared with near-unity photoluminescence quantum yield (PLQY), this is not yet achieved for InP QDs. Treatments with HF have been used to boost the PLQY of InP core-only QDs up to 85%. However, HF etches the QDs, causing loss of material and broadening of the optical features. Here, we present a simple postsynthesis HF-free treatment that is based on passivating the surface of the InP QDs with InF3. For optimized conditions, this results in a PLQY as high as 93% and nearly monoexponential photoluminescence decay. Etching of the particle surface is entirely avoided if the treatment is performed under stringent acid-free conditions. We show that this treatment is applicable to InP QDs with various sizes and InP QDs obtained via different synthesis routes. The optical properties of the resulting core-only InP QDs are on par with InP/ZnSe/ZnS core-shell QDs, with significantly higher absorption coefficients in the blue, and with potential for faster charge transport. These are important advantages when considering InP QDs for use in micro-LEDs or photodetectors.

Optimized preparation of Ni-Febm bimetallic particles by ball milling NiSO4 and iron powder for efficient removal of triclosan

The excessive usage and emissions of triclosan (TCS) pose a serious threat to aquatic environments. Iron-based bimetallic particles (Pd/Fe, Ni/Fe, and Cu/Fe, etc.) were widely used for the degradation of chlorophenol pollutants. This study proposed a novel synthesis method for the preparation of Ni/Fe bimetallic particles (Ni-Febm) by ball milling microscale zero valent iron ZVI (mZVI) and NiSO4. Ball-milling conditions such as ball-milling time, ball-milling speed and ball-to-powder ratio were optimized to prepare high activity Ni-Febm bimetallic particles. During the ball-milling process, Ni2+ was reduced to Ni0 and formed a coupled structure with ZVI. The amount of Ni0 on ZVI significantly affected the activity of Ni-Febm bimetallic particles. The highest activity Ni-Febm bimetallic particles with Ni/Fe ratio of 0.03 were synthesized under optimized conditions, which could remove 86.56% of TCS (10 μM) in aerobic aqueous solution within 60 min. In addition, higher particle dosage, lower pH condition and higher reaction temperature were more conducive for TCS degradation. The higher corrosion current and lower electron transfer impedance of Ni-Febm bimetallic particles were the main reasons for its high activity. The hydrogen atom (•H) on the surface of Ni-Febm bimetallic particles was mainly contributed to the removal of TCS, as reductive transformation products of TCS were detected by LC-TOF-MS. Notably, a small amount of oxidation products were discovered. The total dechlorination rate of TCS was calculated to be 39.67%. After eight reaction cycles, the residual Ni-Febm bimetallic particles could still degrade 28.34% of TCS within 6 h. Low Ni2+ leaching during reaction indicated that Ni-Febm bimetallic particles did not pose potential environmental risks. The prepared environmental-friendly Ni-Febm bimetallic particles with high activity have great potential in the degradation of other chlorinated organic compounds in wastewater.

Leaching kinetics of ash impurities from aphanitic graphite by combining dual-ultrasound and hydrochloric acid–potassium hydrogen fluoride

The hydrochloric acid-fluoride salt is useful for purifying graphite. Ultrasonic-assisted technique can significantly reduce the leaching time and improve the leaching efficiency. Compared with single-frequency, dual-frequency ultrasound has the advantages of high energy efficiency and wide cavitation area. In this study, the combination of a dual-frequency ultrasound-assisted technique and hydrochloric acid–potassium hydrogen fluoride leaching agent was proposed for the leaching of aphanitic graphite to remove impurity minerals. First, the effects of probe-type ultrasonic power, tank-type ultrasonic power, temperature, HCl concentration, ultrasonication time, and KHF2 concentration on the purification efficiency of impurities from aphanitic graphite with the assistance of dual-frequency ultrasound were investigated. It was found that the combination of dual-frequency ultrasound and hydrochloric acid–potassium hydrogen fluoride can reduce the ash content of aphanitic graphite from 13.02 % to 1.02 % with an ash removal rate of 94.17 %. Second, volumetric reaction models and unreacted shrinkage nucleation models were used to fit the kinetics of impurities from aphanitic graphite with dual-frequency ultrasound-assisted HCl-KHF2 leaching. Kinetic analysis shows that the volumetric reaction model with chemical control was better to fit the leaching process. This is consistent with the calculation results of the activation energy of the reaction (Ea = 58.13 kJ/mol). Finally, laser particle size analyzer, X-ray diffraction (XRD), scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), X-ray fluorescence spectroscopy (XRF), transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDS) were used to analyze the fugacity of impurity minerals during the process of dual-frequency ultrasound-assisted HCl-KHF2 leaching. It was revealed that combining ultrasonic cavitation fragmentation with chloric acid–potassium fluoride generated SiF4 with high solubility, thereby removing silica-bearing impurities more efficiently. The challenges in further reducing ash content from 1.02 % in the leached concentrate of aphanitic graphite could be attributed to the existence of titanium-bearing mineral impurities on the surface of graphite particles and the presence of silica-bearing minerals between graphite carbon layers.

Microencapsulation of Origanum heracleoticum L. and Thymus vulgaris L. essential oils – novel strategy to combat multi-resistant Acinetobacter baumannii

Within the global rise of antimicrobial resistance enhanced by the COVID-19 pandemic, where Acinetobacter baumannii has been distinguished as an emerging multi-resistant pathogen, essential oils, become the focus of novel therapeutic approaches. Hypothesizing that encapsulated Origanum heracleoticum L. and Thymus vulgaris L. essential oils could express multi-target approach against A. baumannii, this study aimed to develop microencapsulated systems with optimal technological qualities using 2-hydroxypropyl-β-cyclodextrin as a carrier, and to evaluate their pharmacological potential against A. baumannii, and their morphological and physicochemical characteristics, safety and stability profiles. The highest yield and encapsulation efficiency were obtained with 1:10 essential oil to carrier, and 1.5:10 carrier to water w/w ratios. The formation of inclusion complexes was confirmed by Fourier Transform Infrared Spectroscopy. Both microencapsulates achieved improved homogeneity, particle surface, and thermal stability compared with the pure carrier. Dominant bioactive compounds (carvacrol and p-cymene in O. heracleoticum essential oil, and thymol and p-cymene in T. vulgaris essential oil) remained the most abundant after encapsulation. While non-encapsulated essential oils revealed similar antimicrobial activity towards clinical A. baumannii isolates obtained from COVID-19 patients, encapsulated O. heracleoticum essential oil inhibited the bacterial growth at lower concentrations than T. vulgaris essential oil microencapsulate. All samples significantly reduced the formation of A. baumannii biofilm, for at least 53.90% towards the most infective isolate according to the Caenorhabditis elegans assay. Further, in silico molecular docking study revealed strong interaction pattern of carvacrol and thymol with the outer membrane protein A, which is the main factor for the A. baumannii biofilm formation. Cytotoxicity investigation on human lung A549 cells showed high survival rate in the presence of all tested concentrations, and the stability study revealed notable preservation of the bioactives’ content and pharmacological potential. Altogether, microencapsulated essential oils exhibited a multi-target approach towards A. baumannii, with satisfactory preserving capability during storage.

Mechanistic study of the effects of ultrafine grinding on the surface properties of anthracite coal particles and interface regulation on froth flotation under multifactorial influences

Anthracite, a valuable and scarce coal, typically requires systematic liberation for deep deashing, wherein the particle size reduces to the micron level upon ultrafine grinding. Changes in the physicochemical properties of anthracite particles induced by ultrafine grinding significantly impact subsequent flotation. Accordingly, in this study, a scanning electron microscopy (SEM)-energy-dispersive X-ray spectroscopy (EDS) system, an Opton IPCAS maceral analyzer, a high-sensitivity microelectromechanical balancer, and an X-ray photoelectron spectrometer (XPS) were employed to investigate the changes in the physicochemical properties of the anthracite particle surface during ultrafine grinding. The flotation efficiency of ultrafine anthracite coal is determined by various factors such as the extent of sample liberation, surface wettability, and the state of inorganic mineral coatings. During the initial phase of ultrafine grinding, the comminution efficiency of the sample is high, leading to a progressive increase in the hydrophobicity. However, suboptimal flotation performance results from inadequate liberation. When the sample is liberated to an ultrafine scale, a higher degree of liberation is achieved. The particle surfaces become increasingly covered with inorganic minerals, accompanied by intensified oxidation, leading to a gradually reduced particle hydrophobicity that impaired the flotation performance. This study advances our knowledge on the mechanism by which ultrafine grinding alters the physicochemical properties of anthracite coal particles and affects the flotation processes. The theoretical framework of this study provides crucial insights for interface regulation in the preparation of ultra-low ash anthracite coal and ultrafine coal flotation.

Building an Elastic Mechanical Network for Highly Efficient Silicon‐Based Anodes

AbstractSilicon (Si), known for its high theoretical capacity, holds promise for developing high‐energy‐density lithium‐ion batteries (LIBs). However, the intrinsic low conductivity and substantial volume expansion limit its commercial application. Developing a binder that can suppress the massive volume expansion while improving Si conductivity is particularly important for LIBs based on Si anode. Here, grafting natural adhesive cationic guar gum (CGG) with small molecular acrylamide (AM) is proposed and applied it to the Si‐based anode. The rigid guar gum main chain and the elastic polymerized acrylamide (pAM) side chain forms a 3D network that completely encapsulated Si nanoparticles and cross‐linked with the natural hydroxyl groups on the surface of Si particles through abundant functional groups. Numerous link anchors and robust mechanical networks facilitate lithium‐ion transport and effectively mitigated the significant stress generated by silicon during charge and discharge cycles. Based on this innovative design, the Si@CGG@pAM@SP (Super P) electrode demonstrates excellent long‐term cycle stability and rate performance. The Si@CGG@pAM@SP electrode preserves 2086 mAh g−1 discharge capacity after 100 cycles (corresponding to 91.5% capacity retention). Physical characterization and electrochemical tests confirm the rationality of the polymer binder design, serving as a valuable reference for the material design of lithium‐ion batteries.

Influence of raw material properties on microscopic and mechanical characteristics of alkali-activated materials

Alkali-activated fly ash and slag pastes are considered a new low-carbon cementitious material with good mechanical characteristics and durability. However, the mechanical characteristics of the alkali-activated materials are uncertain due to the multiplicity of the raw material properties. Few studies clarify how the raw material properties affect the mechanical characteristics of hardened pastes. The correlation between the raw material properties and the reaction rate, product composition, gel content, and pore size distribution is discussed in this study. The increase in the CaO content of the precursor will accelerate the degree of alkali activation. In this case, the reaction production becomes relatively more, and the pore size distribution becomes relatively denser, improving the compressive strength of the pastes. Moreover, the effects of the activator modulus and alkali content on the compressive strength of the pastes are not monotonically increasing. The excessive alkali will cause the surface of raw material particles to form a gel layer quickly, which could prevent the further alkali activation of the particles. This case is not conducive to gel formation and will cause the pore structure of the hardening pastes to be relatively loose. Furthermore, the influence of activator modulus on the compressive strength of pastes is lower than that of alkali content. Excess activator modulus is also unfavourable for pore structure densification.

PH- and Photoresponsive Liquid Plasticine.

Liquid marbles (LMs) can be prepared by adsorption of hydrophobic particles at the air-liquid interface of a water droplet. LMs have been studied for their application as microreaction vessels. However, their opaqueness poses challenges for internal observation. Liquid plasticines (LPs), akin to LMs, can be prepared by the adsorption of hydrophobic particles with a diameter of 50 nm or less, at the air-liquid interface of a water droplet. Unlike LMs, LPs are transparent, allowing for internal observation, thus presenting promising applications as reactors and culture vessels on a microliter scale. In this study, the surface of silica particles, approximately 20 nm in diameter, was rendered hydrophobic to prepare hydrophobic silica particles (SD0). A small amount of poly(2-(diisopropylamino)ethyl methacrylate) (PDPA) was then grafted onto the surface of SD0, yielding SD1. SD0 particles exhibited consistent hydrophobicity irrespective of the environmental pH atmosphere. Under acidic conditions, SD1 became hydrophilic due to the protonation of pendant tertiary amines in the grafted PDPA chains. However, SD1 alone was unsuitable for LP preparation due to its high surface wettability regardless of atmospheric pH, attributable to the presence of PDPA-grafted chains. Therefore, to prepare pH-responsive LP, SD1 and SD0 were mixed (SD1/SD0 = 3/7). Upon exposure to HCl gas, these LPs ruptured, with the leaked water from the LPs being absorbed by adjacent paper. Moreover, clear LPs, prepared using an aqueous solution containing a water-soluble photoacid generator (PAG), disintegrated upon exposure to light as PAG generated acid, leading to LP breakdown. In summary, pH-responsive LPs, capable of disintegration under acidic conditions and upon light irradiation, were successfully prepared in this study.