Carbon Particles Research Articles

Steam Gasification of PEMFC Catalysts: An Endothermal Process to Create Accessible Carbon Support Morphologies

Platinum catalysts supported on porous carbons are considered state-of-the-art for proton-exchange membrane fuel cells (PEMFCs) due to their ability to protect Pt nanoparticles within the internal pores of the primary carbon particles. This shielding enables high oxygen reduction reaction (ORR) activity by separating the Pt particles from ionomer contact and endows them with greater resilience against voltage cycling-induced degradation. However, the pore enclosure impedes oxygen diffusion to internal platinum particles at high current densities, incurring significant voltage losses particularly at low cathode loadings (∼0.07 mgPt cm−2). Such transport bottlenecks can be mitigated by localized oxidation, a thermal post-treatment enabling Pt particles to etch open the surrounding pore space via Pt-catalyzed carbon oxidation. The strong exothermicity of this reaction, however, is challenging for process scale-up. We explore Pt-catalyzed steam gasification of Pt/Ketjenblack as an endothermal, but otherwise functionally similar post-treatment to increase catalyst accessibility. Connecting physico- and electrochemical characterizations of steam-gasified catalysts, we identify the generation of mesopore volume to be crucial for high current density performance and efficient oxygen transport. Ultimately, locally oxidized and steam-gasified catalysts reveal subtle differences in their respective etching mechanisms, resulting in marginally less efficient pore opening, but also better ORR activity retention for steam gasification.

Carbon Nanotubes an Excellent Targeted Drug Delivery System

Carbon nanotubes, or CNTs, are carbon allotropes with a nanostructure that can have a length-to-breadth proportion more prominent than 1,000,000. These round and hollow carbon particles have exceptional properties that make them possibly helpful in an assortment of nanotechnology applications. CNTs might be joined with a scope of natural components, including proteins, drugs, and nucleic acids, to give bio-functionalities. CNTs come in two assortments: multi-walled (MWNTs) and single-walled (SWNTs). Among its captivating properties are its high viewpoint proportion, strength, lightweight weight, high warm conductivity, and electrical attributes that reach from metallic to semiconducting. Carbon nanotubes might be made by various cycles, including warm blend, substance fume statement, laser removal, circular segment release dissipation, plasma-based union, and synthetic fume affidavit increased by plasma. Carbon nanotubes (CNTs) track down use in drug conveyance, blood malignant growth, bosom disease, cerebrum malignant growth, liver malignant growth, cervical malignant growth, quality treatment, resistant therapy, biomedical imaging, biosensors, and tissue designing. The noncovalent functionalization of specific MNTs with folic corrosive (FA) worked on the vehicle of medication to malignant growth cells in the lymph hubs. By utilizing a remotely introduced magnet to guide the medication lattice to the provincial designated lymph hubs, the MNTs can ceaselessly deliver chemotherapeutic medications for a few days while remaining in the depleting designated lymph hubs. Growth cells communicating folate receptors (FRs) in the lymph hubs can be explicitly obliterated since FRs are overexpressed in different human malignancies.

P21-30 Effects of black carbon particles on human monocyte-derived macrophages in vitro

P21-30 Effects of black carbon particles on human monocyte-derived macrophages in vitro

Discrete Element Study on Mechanical Properties of MICP-Treated Sand under Triaxial Compression

Microbial-induced calcium carbonate precipitation (MICP) has attracted much attention as a promising technology for soil improvement in the infrastructures of marine engineering. This paper introduces a novel numerical sample preparation technique for MICP-treated sand, with particular attention paid to the distribution patterns of calcium carbonate, including contact cementing, bridging, and grain coating. The effect of calcium carbonate content (CCC) on the deformation and failure mechanism is studied at macroscopic and granular scales. The findings show that a small amount of calcium carbonate can quickly increase the strength of sand. The strength improvement and deformation control of MICP technology are better than those of traditional compaction treatment. As the calcium carbonate content increases, the mechanical coordination number of the sand also increases, indicating a more stable microstructure of the sand phase. In the contact bonding mode, initial failure occurs as shear failure between sand and calcium carbonate. In the bridge mode, initial failure manifests as shear failure between calcium carbonate particles. In the coating mode, initial failure occurs as tensile failure between sand and calcium carbonate. Calcium carbonate contributes to a reduction in both sliding and rolling movements among sand particles.

Macroscale vertical power-law distribution of bacteria in dark oceans can emerge from microscale bacteria-particle interactions

Microbes in the dark oceans are a key determinant of remineralization of sinking carbon particles. However, most marine ecosystem models overlook how microbes aggregate on particles and the microscale interactions between particle-associated microbes, making it difficult to obtain mechanistic insights on their vertical power-law decay pattern. Here, we present a spatial population model where the attachment and detachment processes of bacterial cells depend on local density of particle-associated bacteria. We show that the power-law relationship can emerge when the non-random aggregated distribution of bacteria is considered without any depth-specific environmental parameters. Furthermore, the comparison between model behavior and empirical patterns in the Pacific and Southern Ocean indicated that temperature-dependent hydrolysis rate and nutrient-dependent sinking rate of particles are key parameters to explain the regional variations of the power-law exponent. The mechanistic approach developed here provides a pathway to link micro-scale interactions between individuals to macro-scale food chain structures and carbon cycle

Enhancing hydrovoltaic power generation with carbon spheres coated on nickel foam/polyethylene terephthalate substrate

The present study aims to assess the viability of hydrovoltaic impact as a potential method for energy generation. This methodology utilizes the capillary action of water in devices composed of nickel (Ni) foam/polyethylene terephthalate (PET) substrates coated with hydrothermally synthesized carbon spheres at various temperatures (180, 200, and 220 °C). The prepared materials and devices were analyzed using a range of analytical techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FTIR). The SEM images revealed the spherical morphology of the carbon particles and their presence on Ni foam, whereas the XRD patterns indicated that the carbon spheres were amorphous. Spectroscopic analysis revealed the presence of hydroxyl functional groups in all the samples. The performance of the devices was assessed by electrochemical tests, including open-circuit potential (OCP), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The device coated with carbon spheres synthesized at 180 °C demonstrated enhanced performance with an elevated OCP value of 0.077 V, increased surface charge area, lower resistance to water, and reduced charge transfer resistance. These findings indicate the successful production of hydrovoltaic energy by utilizing the capillary action of water in carbon-sphere-coated Ni foam/PET devices.

NEUROTOXIC RISK AND ADSORPTION PROPERTIES OF COARSE NON-FUNCTIONALIZED CARBON PARTICLES DERIVED FROM APPLE WASTE

Aim. Carbon particles have been widely used in different technologies and have great potential for new biological application. Synthesis of carbon particles from agricultural waste using “green” principles is in the mainstream of biotechnology area and attract a great attention in biomedical application. Here, coarse carbon particles (CCPs) were synthesized using “green” principles from dry apple and used in the biological experiments without preliminary functionalization. Methods. Neurotoxic features of CCPs were analysed in isolated presynaptic cortex nerve terminals (synaptosomes) monitoring the extracellular levels of excitatory neurotransmitter L-[14C] glutamate and inhibitory one [3H]GABA, as well as the membrane potential. Results. Measuring the membrane potential of the nerve terminals, it was revealed an inadequate decrease in the fluorescence intensity of the potential-dependent dye rhodamine 6G in the presence of CCPs (1 mg/ml). This decrease was not due to membrane hyperpolarisation because CCPs did not change the extracellular synaptosomal levels of L-[14C] glutamate and [3H]GABA. CCP-induced decrease in the fluorescence intensity of the dye in nerve terminals can be due to its interaction with CCPs. Indeed, the ability of CCPs to interact with rhodamine 6G was shown in synaptosome-free incubation media. Conclusions. Therefore, CCPs did not possess neurotoxic signs, and so are biocompatible. In both experiments, i.e. without bio object and in biological system, CCPs were able to interact with fluorescent dye rhodamine 6G. In prospect, this feature of CCPs can be used in biotechnology after further investigation of dye interaction conditions.

Development and application of metal–organic frameworks and spherical carbon particles for efficient recovery of phenols and oils from coal chemical wastewater: A new full-process adsorption treatment mode

To address the challenges of high energy consumption and low efficiency in recovering phenols and oils from coal chemical wastewater (CCW), this study focused on the design and synthesis of metal–organic frameworks and spherical carbon particle (MOFs/SCP) adsorbents with a high adsorption capacity and ease of desorption. Additionally, a new comprehensive treatment mode named “adsorption-desorption-regeneration-recovery” (ADRR) was developed to efficiently recover phenols and oils from CCW. The results revealed that the ADRR treatment mode maintained high adsorption and desorption efficiencies of MOFs/SCP, which remained consistently above 95 %. Additionally, methanol regeneration reached ∼ 90 %, and the recovery efficiency of phenols and oils was ∼ 83 %. The analysis of the adsorption behavior model indicated that the adsorption of phenols and oils by MOFs/SCP mainly involved monolayer chemical adsorption characterized by spontaneity, heat absorption, and disorder. The dynamic adsorption model exhibited a strong correlative ability to predict and assess the adsorption capacity, rate, equilibrium, and operating parameters. Finally, structural analyses and molecular dynamics simulations revealed that the micro-interaction mechanisms between MOFs/SCP and phenols and oils mainly depended on the distinctive hydrophobic nature and porous adsorption capabilities of MOFs/SCP. These interactions were mainly facilitated by electrostatic interactions, π–π interactions, and hydrogen bonding. The findings of the study are crucial for achieving high-value recovery of phenols and oils from CCW and, promoting the clean and sustainable growth of the coal chemical industry.

Linking the size of hard carbon particles with electrochemical response in sodium ion storage

Hard carbon is considered to be one of the most promising anodes for sodium-ion batteries (SIBs) owing to its high capacity and abundant resources. However, the role of particle size on sodium ion storage is unclear, which leads to low capacity and initial coulombic efficiency (ICE) in practical application. In this work, a series of hard carbons with different particle sizes were prepared by an “up to down” strategy using simple grinding and ball-milling method to investigate the effect of particle size on electrochemical response of sodium ion storage. The particle size of hard carbon has negligible effect on initial specific capacity. However, it has a strong effect on the ICE and rate capability. The ICE reduces as the particle size decreases, but the rate performance in reverse. Moreover, impedance analysis and electrochemical kinetics show huge differences for different particle sizes. In-situ Raman technique was also adopted to further illustrate the sodium ion storage mechanism of hard carbon, and an “adsorption-intercalation-pore filling” mechanism is proposed. This work could provide a new perspective for the design of hard carbon materials with suitable structure for efficient sodium ion storage, helping to develop high performance SIBs.

Hard carbon/graphene microfibers as a superior anode material for sodium-ion batteries

Hard carbon is one of the most promising anode materials for sodium-ion batteries (SIBs). However, it still suffers from low specific capacity and poor rate capability, which impede its practical application. Herein, one-dimensional hard carbon/graphene microfibers are synthesized by encapsulating hard carbon particles in graphene nanosheet using a wet-spinning technique followed by pyrolysis treatment. Benefiting from the unique structure, when used as the anode material for SIBs, the as-obtained hard carbon/graphene microfibers not only exhibit a high reversible capacity of 321 mAh g−1 at 0.1 C but also deliver long cycling stability and excellent rate capability, maintaining its capacity as 203 mAh g−1 even after 350 cycles at 1 C. In addition, the sodium storage mechanism of the as-prepared hard carbon/graphene microfibers is investigated by in-situ Raman technique. Moreover, a full cell adopting the hybrid microfiber as the anode and Na3V2(PO4)3 as the cathode exhibits high specific capacities of 291 mAh g−1 and 204 mAh g−1 at 0.2 C and 4 C (vs. anode), respectively. This work provides a sustainable and cost-effective strategy for the synthesis of high-capacity and stable hard carbon anode materials.

Visualization experiment on dynamic migration and sealing mechanism of irregular materials in rough fractures

Lost circulation is one of the main problems causing low drilling efficiency and high drilling costs in the oil and gas industry. Due to an insufficient understanding of the migration and sealing mechanism of lost circulation materials (LCMs) in rough fractures, the success of fracture sealing is highly unpredictable. This study conducted visualization experiments using four types of LCMs to observe the entire dynamic sealing process of rough fractures. Adaptive fracture sealing experiments were designed to improve the sealing performance of LCMs at low concentrations. The results indicated that the key to sealing rough fractures is forming an effective sealing zone inside the fracture space rather than in the inlet buffer zone. The dynamic sealing process has experienced four typical stages: sporadic bridging, bridging structure expansion, sealing front formation, and sealing layer thickening. The first three typical stages correspond to flow from plate flow to trench flow and seepage. The formation of an effective sealing zone within fractures depends on forming a practical sealing front and subsequent particle accumulation of LCMs that thicken the sealing layer. Compared with regular particles, the sealing front of irregular particles is an area with a specific aperture range. The increase in irregular particle concentration makes the sealing front migrate to the fracture entrance, which is more likely to lead to inlet blockage. The distribution of a sealing zone depends upon the surface morphology of rough fracture. Increasing the particle size distribution improves the favorable bridging area and enhances the sealing performance. The adaptive sealing strategy uses low-concentration granular materials to form multi-point bridging within rough fractures and low-concentration flaky materials to adaptively and quickly extend and connect dispersed bridging structures. Mica flakes are more conducive to extending along the contour of fracture aperture than calcium carbonate particles. Adding mica flakes promotes the expansion of the bridging structures, forming a sealing front and a robust sealing layer in advance. This study delves into irregular materials' migration and sealing mechanisms in rough fractures, enriching theoretical understanding and providing guidance for on-site sealing operations.

In-situ co-growth of ZIF-8-derived bio-carbon spheres with meso-macroporous hierarchy for stable and rapid carbon dioxide capture

Efficient carbon dioxide (CO2) capture from post-combustion flue gases is crucial for industrial applications. Adsorbents with high adsorption capacity, exceptional stability, high selectivity, and low cost are essential to meet these requirements. In this study, we present the synthesis of bio‑carbon spheres derived from zeolitic imidazolate framework-8 (ZIF-8) using a macro-fluidic technique. The bio‑carbon spheres integrate ZIF-8 for structural orientation and chitosan for the directional assembly of ZIF-8, thereby addressing the limitations of low strength in chitosan-derived carbon spheres and the challenge of macroscopic shaping of ZIF-8 particles. Additionally, the incorporation of ZIF-8 and the enhancement of the carbon skeleton increased the meso-macroporosity, improving CO2 transport and adsorption performance. The bio‑carbon spheres demonstrated a 46.9% higher CO2 adsorption capacity (101 kPa, 1.40 mmol·g−1) compared to pure chitosan carbon granules (101 kPa, 0.96 mmol·g−1) and a 17.8% faster mass transport rate compared to ZIF-8 carbon particles. Moreover, the bio‑carbon spheres exhibit a low wear rate in a simulated fluidized bed, good thermal stability, and stable cyclic regeneration performance. This study offers a novel strategy for developing industrially applicable adsorbents with hierarchical pore structures to enhance CO2 capture.

Nitrogen-doped iron-manganese porous carbon particle electrodes for electrocatalytic degradation of tetracycline: Interfacial reaction mechanisms

In this study, nitrogen-doped porous carbon-supported iron-manganese microspheres (FeMn@NC-700) were successfully synthesized and employed as three-dimensional particle electrodes (3DPE) for electro-oxidative of tetracycline (TCH) in water. FeMn@NC-700 exhibited stable catalytic activity and effective TCH removal capabilities under complex water quality conditions and varying pH levels. Under optimized conditions, the 3D/FeMn@NC-700 system reduced the TCH concentration from an initial 20 mg/L to 0.96 mg/L within 60 min, achieving a 95.23 %removal efficiency with an energy consumption of only 10.05 kWh/m3. The outstanding electrocatalytic activity of the 3D/FeMn@NC-700 system was attributed to the dynamic redox cycling between the Fe and Mn species on the 3DPE surface. Radical quenching experiments and electron paramagnetic resonance (EPR) analysis identified the predominant role of singlet oxygen (1O2), effectively removing TCH with the assistance of hydroxyl radicals (·OH) and superoxide anions (O2·-). The degradation pathways of major intermediate products of TCH were proposed, along with a toxicity assessment. In conclusion, the 3D/FeMn@NC-700 system represents a reliable and cost-effective technology for TCH wastewater treatment.

Optimized Porous Carbon Particles from Sucrose and Their Polyethyleneimine Modifications for Enhanced CO2 Capture

Carbon dioxide (CO2), one of the primary greenhouse gases, plays a key role in global warming and is one of the culprits in the climate change crisis. Therefore, the use of appropriate CO2 capture and storage technologies is of significant importance for the future of planet Earth due to atmospheric, climate, and environmental concerns. A cleaner and more sustainable approach to CO2 capture and storage using porous materials, membranes, and amine-based sorbents could offer excellent possibilities. Here, sucrose-derived porous carbon particles (PCPs) were synthesized as adsorbents for CO2 capture. Next, these PCPs were modified with branched- and linear-polyethyleneimine (B-PEI and L-PEI) as B-PEI-PCP and L-PEI-PCP, respectively. These PCPs and their PEI-modified forms were then used to prepare metal nanoparticles such as Co, Cu, and Ni in situ as M@PCP and M@L/B-PEI-PCP (M: Ni, Co, and Cu). The presence of PEI on the PCP surface enables new amine functional groups, known for high CO2 capture ability. The presence of metal nanoparticles in the structure may be used as a catalyst to convert the captured CO2 into useful products, e.g., fuels or other chemical compounds, at high temperatures. It was found that B-PEI-PCP has a larger surface area and higher CO2 capture capacity with a surface area of 32.84 m2/g and a CO2 capture capacity of 1.05 mmol CO2/g adsorbent compared to L-PEI-PCP. Amongst metal-nanoparticle-embedded PEI-PCPs (M@PEI-PCPs, M: Ni, Co, Cu), Ni@L-PEI-PCP was found to have higher CO2 capture capacity, 0.81 mmol CO2/g adsorbent, and a surface area of 225 m2/g. These data are significant as they will steer future studies for the conversion of captured CO2 into useful fuels/chemicals.

Crosslinked polyethyleneimine‐based structures in different morphologies as promising CO2 adsorption systems: A comprehensive study

AbstractAlthough there are many studies on CO2 adsorption via PEI‐modified carbon particles, metal–organic frameworks, zeolitic imidazolate frameworks, and silica‐based porous structures, only a limited number of studies on solely cross‐linked PEI‐based structures. Here, the CO2 adsorption capacities of PEI‐based microgels and cryogels were investigated. The effects of various parameters influencing the CO2 adsorption capacity of PEI‐based structures, for example, crosslinker types, PEI types (branched [bPEI] or linear [lPEI]), adsorbent types (microgel or cryogel), chemical‐modification including their complexes were examined. NaOH‐treated glycerol diglycidyl ether (GDE) crosslinked lPEI microgels exhibited higher CO2 adsorption capacity among other microgels with 0.094 ± 0.006 mmol CO2/g at 900 mm Hg, 25°C with 2‐ and 7.5‐fold increase upon pentaethylenehexamine (PEHA) modification and Ba(II) metal ion complexing, respectively. The CO2 adsorption capacity of bPEI and lPEI‐based cryogels were compared and found that lPEI‐GDE cryogels had higher adsorption capacity than bPEI‐GDE cryogels with 0.188 ± 0.01 mmol CO2/g at 900 mm Hg and 25°C. The reuse studies revealed that NaOH‐treated GDE crosslinked bPEI and lPEI microgels and cryogels showed promising potential, for example, after 10‐times repeated use >50% CO2 adsorption capacity was retained. The results affirmed that PEI‐based microgels and cryogels are encouraging materials for CO2 capture and reuse applications.

Fabrication of biocomposite materials with polycaprolactone and activated carbon extracted from agricultural waste

In this study, activated carbon was extracted from a source of agricultural waste (wheat straw) through a chemical activation process and blended with polycaprolactone (PCL) to fabricate new biocomposite materials. Three distinct types of activated carbon, designated as C1, C2, and C3 were obtained by varying the ratio of the activation agent and wheat straw and different drying conditions. Through a comprehensive array of analytical techniques, including FTIR, XRD, BET, EDS, and FE-SEM, we determined the optimal experimental method for extracting activated carbon from wheat straw and identified the most effective type of activated carbon (C3). Based on these analyses, C3 exhibits the highest carbon content, the greatest specific surface area (386.47 m2/g), and the highest total pore volume (0.2596 cm3/g). By blending polycaprolactone with the optimal activated carbon (at concentrations of 1, 3, and 5 wt%), biocomposite samples were fabricated. The results of FTIR indicate that the biocomposite materials containing 1, 3, and 5 wt% of activated carbon exhibit no disturbing peaks. However, the sample PCL-C,1 wt%, shows significant increases in the intensity of observed peaks. XRD analyses of the fabricated biocomposite samples illustrate that the sample containing 1 wt% of activated carbon has a greater tendency for crystallization compared to the other samples. Morphological analysis of the biocomposites and the dispersion of carbon particles within them demonstrate the least amount of agglomeration in the sample with an activated carbon concentration of 1 wt%. Upon assessing the mechanical properties of biocomposites, the same sample (1 wt% of C3) demonstrates more favorable characteristics than the other samples. Furthermore, a contact angle test was conducted to gauge the biocomposite hydrophilicity, revealing a 7 degree increase in contact angle for the sample with an activated carbon concentration of 1 wt% compared to the pure PCL sample. Thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to examine the weight loss, degradation temperature, melting temperature, and glass transition temperature of the synthesized materials. These analyses indicate a marginal augmentation in both melting and glass transition temperatures for the sample with an activated carbon concentration of 1 wt%.

Assessment of vertical transport of PM in a surface iron ore mine due to in-pit mining operations

Particulate matter (PM) is the most prevalent pollutant associated with surface mining operations, adversely affecting the health of mine workers. Using a combination of low-cost PM sensors and portable sampling devices, this research quantified the PM concentration and factors influencing its vertical transport inside a 100 m deep surface iron ore mine.Transport of ore through off-road trucks accounted for ∼ 70 % of the in-pit emissions. Also, differential settling and varying meteorological parameters along the vertical extent of the mine resulted in the escape of 17 % of PM2.5-10, 43 % of PM1-2.5, and 69 % of PM1to the mine’s surrounding atmosphere. Iron ore and carbon particles were identified as the major constituents of the airborne PM. The findings of this study demonstrate the application of low-cost sensors in monitoring PM concentration along the vertical extent of the mine, which can ultimately provide exposure estimates to the mine workers at different working locations.

A comparative study of first and second generation biodiesel blends under quaternary injection strategies for enhanced engine performance and reduced emissions

Biodiesel is a promising renewable alternative fuel, offering compatibility with conventional engines without necessitating significant engine modifications. To facilitate the practical integration of biodiesel into engine systems, this study evaluates the performance of two different biodiesel blends (fatty acid methyl ester and hydrogenated catalytic) in a turbocharged inter-cooled diesel engine. The research employs quaternary injection techniques an advanced injection technique, which involve multiple injection events per cycle to enhance engine combustion and emission characterictics of the biodiesel blend fuels and comparing their performance and emission characteristics with those of conventional diesel. Results showed that fatty acid methyl ester biodiesel effectively reduced the CO, UHC, and NOx emissions at lower blend ratios (up to 10 %), with minimal impact on the brake-specific fuel consumption. Conversely, hydrogenated catalytic biodiesel demonstrates notable advantages in reducing fuel consumption with carbon monoxide and particle emissions, particularly for higher blend ratios (20 %), leading to improved indicated thermal efficiency. Additionally, an investigation on higher biodiesel blends under varying early injection timings showed that, optimal fuel efficiency was observed at an early injection timing of −43.6 °CA, accompanied by reductions in total particle number and unburned hydrocarbon emissions albeit with elevated carbon monoxide and nitrogen oxide emissions. These findings suggest that advanced injection strategies combined with sustainable biodiesel blends can significantly improve engine performance and reduce environmental impact, supporting the transition towards cleaner and more efficient transportation fuels.

Multiple-charging effects on the CCN activity and hygroscopicity of surrogate black carbon particles

Accurate measurements of cloud condensation nuclei (CCN) activity and hygroscopicity of black carbon (BC)-containing particles are particularly important because of the positive climate forcing from these particles. Such measurements are typically conducted on particles selected by a Differential Mobility Analyzer (DMA), which in addition to singly charged particles transmits multiply charged larger particles that have the same electrical mobility. These larger particles activate at lower supersaturations than the singly charged particles, biasing measurements and resulting in overestimation of CCN activity and hygroscopicity parameter (κ). Here, we measure the CCN activity and determine κ for different BC surrogates with electrical mobility diameters from 100 to 200 nm selected 1) only by electrical mobility with a DMA, and 2) by both electrical mobility and mass using a DMA and a Centrifugal Particle Mass Analyzer (CPMA), thus allowing selection of only singly charged particles. We demonstrate the use of the DMA-CPMA system in resolving biases caused by multiply charged particles, and we show that the effect of multiple charging on the CCN activity of the BC particles is strongly influenced by morphology dispersion, i.e., the variability due to the range of morphologies of particles that have the same electrical mobility and mass. Our findings show that electrical mobility-based methods alone are unlikely to lead to accurate results in measurements of CCN activation and hygroscopicity of BC particles, even for those with a more compact morphology.

Stress and flow inhomogeneity in shear-thickening suspensions

HypothesisThe viscosity of dense suspensions surges when the applied stress surpasses a material-specific critical threshold. There is growing evidence that the thickening transition involves non-uniform flow and stress with considerable spatiotemporal complexity. Nevertheless, it is anticipated that dense suspensions of calcium carbonate particles with purely repulsive interactions may not conform to this scenario, as indicated by local pressure measurements with millimeter spatial resolution. ExperimentHere we utilize Boundary Stress Microscopy (BSM), a technique capable of resolving stresses down to the micron scale, to search for evidence of stress heterogeneity. In addition, we measure the flow field at the lower boundary of the suspension where the boundary stress is measured. FindingsWe find localized regions of high-stresses that are extended in the vorticity direction and propagate in the flow direction at a speed approximately half that of the rheometer's top plate. These high-stress regions proliferate with the applied stress accounting for the increased viscosity. Furthermore, the velocity of particles at the lower boundary of the suspension shows a significant and complex nonaffine flow that accompanies regions of high-stresses. Hence, our findings demonstrate that stress and flow inhomogeneity are intrinsic characteristics of shear-thickening suspensions, regardless of the nature of interparticle interactions.