Concentration Gradient Research Articles

Repurposing discarded leukodepletion filters as a source of mononuclear cells for advanced in vitro research

In light of advancements in the field of immuno-oncology, the demand for obtaining mononuclear cells for in vitro assays has surged. However, obtaining these cells from healthy donors remains a challenging task due to difficulties in donor recruitment and the requirement for substantial blood volumes. Here, we present a protocol for isolating peripheral blood mononuclear cells (PBMCs) from leukodepletion filters used in whole blood and erythrocytes by apheresis donations at the Hemonucleus of the Barretos Cancer Hospital, Brazil. The method involves rinsing the leukodepletion filters and subsequent centrifugation using a Ficoll-Paque concentration gradient. The isolated PBMCs were analyzed by flow cytometry, which allowed the identification of various subpopulations, including CD4+ T lymphocytes (CD45+CD4+), CD8+ T lymphocytes (CD45+CD8+), B lymphocytes (CD45+CD20+CD19+), non-classical monocytes (CD45+CD64+CD14−), classical monocytes (CD45+CD64+CD14+), and granulocytes (CD45+CD15+CD14−). In our comparative analysis of filters, we observed a higher yield of PBMCs from whole blood filters than those obtained from erythrocytes through apheresis. Additionally, fresh samples exhibited superior viability when compared to cryopreserved ones. Given this, leukodepletion filters provide a practical and cost-effective means to isolate large quantities of pure PBMCs, making it a feasible source for obtaining mononuclear cells for in vitro experiments. SummaryHere, we provide a detailed protocol for the isolation of mononuclear cells from leukodepletion filters, which are routinely discarded at the Barretos Cancer Hospital's Hemonucleus.

Large-area, self-healing block copolymer membranes for energy conversion

Membranes are widely used for separation processes in applications such as water desalination, batteries and dialysis, and are crucial in key sectors of our economy and society1. The majority of technologically exploited membranes are based on solid polymers and function as passive barriers, whose transport characteristics are governed by their chemical composition and nanostructure. Although such membranes are ubiquitous, it has proved challenging to maximize selectivity and permeability independently, leading to trade-offs between these pertinent characteristics2. Self-assembled biological membranes, in which barrier and transport functions are decoupled3,4, provide the inspiration to address this problem5,6. Here we introduce a self-assembly strategy that uses the interface of an aqueous two-phase system to template and stabilize molecularly thin (approximately 35 nm) biomimetic block copolymer bilayers of scalable area that can exceed 10 cm2 without defects. These membranes are self-healing, and their barrier function against the passage of ions (specific resistance of approximately 1 MΩ cm2) approaches that of phospholipid membranes. The fluidity of these membranes enables straightforward functionalization with molecular carriers that shuttle potassium ions down a concentration gradient with exquisite selectivity over sodium ions. This ion selectivity enables the generation of electric power from equimolar solutions of NaCl and KCl in devices that mimic the electric organ of electric rays.

Diffusiophoresis in Polymer and Nanoparticle Gradients.

Diffusiophoresis is the movement of the colloidal particles in response to a concentration gradient and can be observed for both electrolyte (e.g., salt) and nonelectrolyte (e.g., glucose) solutes. Here, we investigated the diffusiophoretic behavior of polystyrene (PS-carboxylate surface) microparticles in nonadsorbing charged and uncharged solute gradients [sodium polystyrenesulfonate (NaPSS), polyethylene glycol (PEG), and nanoscale colloidal silica (SiO2)] using a dead-end channel setup. We compared the diffusiophoretic motion in these gradient types with each other and to the case of using a monovalent salt gradient. In each of the nonadsorbing gradient systems (NaPSS, PEG, and SiO2 nanoparticles), the PS particles migrated toward the lower solute concentration. The exclusion distance values (from the initial position) of particles were recorded within the dead-end channel, and it was found that an increase in solute concentration increases exclusion from the main channel. In the polyelectrolyte case, the motion of PS microparticles was reduced by the addition of a background salt due to reduced electrostatic interaction, whereas it remained constant when using the neutral polymer. Particle diffusiophoresis in gradients of polyelectrolytes (charged macromolecules) is quite similar to the behavior when using a PEG gradient (uncharged macromolecule) in the presence of a background electrolyte. Moreover, we observed PS microparticles under different concentrations and molecular weights of PEG gradients. By combining the simulations, we estimated the exclusion length, which was previously proposed to be the order of the polymer radius. Furthermore, the movement of PS microparticles was analyzed in the gradient of silica nanoparticles. The exclusion distance was higher in silica nanoparticle gradients compared to similar-size PEG gradients because silica nanoparticles are charged. The diffusiophoretic transport of the PS microparticles could be simulated by considering the interaction between the PS microparticles and silica nanoparticles.

A Reverse Nonequilibrium Molecular Dynamics Algorithm for Coupled Mass and Heat Transport in Mixtures.

We present a new method for introducing stable nonequilibrium concentration gradients in molecular dynamics simulations of mixtures. This method extends earlier reverse nonequilibrium molecular dynamics (RNEMD) methods, which use kinetic energy scaling moves to create temperature or velocity gradients. In the new scaled particle flux (SPF-RNEMD) algorithm, energies and forces are computed simultaneously for a molecule existing in two nonadjacent regions of a simulation box, and the system evolves under a linear combination of these interactions. A continuously increasing particle scaling variable is responsible for the migration of the molecule between the regions as the simulation progresses, allowing for simulations under an applied particle flux. To test the method, we investigate diffusivity in mixtures of identical but distinguishable particles and in a simple mixture of multiple Lennard-Jones particles. The resulting concentration gradients provide Fick diffusion constants for mixtures. We also discuss using the new method to obtain coupled transport properties using simultaneous particle and thermal fluxes to compute the temperature dependence of the diffusion coefficient and activation energies for diffusion from a single simulation. Lastly, we demonstrate the use of this new method in interfacial systems by computing the diffusive permeability of a molecular fluid moving through a nanoporous graphene membrane.

Proton-driven sodium secretion in a saline water animal

Aquatic animals residing in saline habitats either allow extracellular sodium concentration to conform to environmental values or regulate sodium to lower levels. The latter strategy requires an energy-driven process to move sodium against a large concentration gradient to eliminate excess sodium that diffuses into the animal. Previous studies of invertebrate and vertebrate species indicate a sodium pump, Na+/K+ ATPase, powers sodium secretion. We provide the first functional evidence of a saline-water animal, Aedes taeniorhynchus mosquito larva, utilizing a proton pump to power this process. Vacuolar-type H+ ATPase (VHA) protein is highly expressed on the apical membrane of the posterior rectal cells, and in situ sodium flux across this epithelium increases significantly in larvae held in higher salinity and is sensitive to Bafilomycin A1, an inhibitor of VHA. We also report the first evidence of splice variants of the sodium/proton exchanger, NHE3, with both high and low molecular weight variants highly expressed on the apical membrane of the posterior rectal cells. Evidence of NHE3 function was indicated with in situ sodium transport significantly inhibited by a NHE3 antagonist, S3226. We propose that the outward proton pumping by VHA establishes a favourable electromotive gradient to drive sodium secretion via NHE3 thus producing a hyperosmotic, sodium-rich urine. This H+- driven Na+ secretion process is the primary mechanism of ion regulation in salt-tolerant culicine mosquito species and was first investigated over 80 years ago.

Reduced internal stress of quasi-single crystalline Na4Fe3(PO4)2P2O7 electrode enhancing sodium-ion kinetics

A NASICON-type quasi-single crystalline Na4Fe3(PO4)2P2O7 (SC) cathode material was successfully synthesized via a freeze-drying method. The as-optimized SC sample displays both outstanding rate performance (107.9 and 88.5 mAhg−1 at 0.1C and 5C, respectively) and excellent cycling stability (88.1 % of capacity retention after 1000 cycles at 1C). Reduced sodium ion migration path of as-prepared SC cathode material effectively enhanced the kinetics of Na+ upon cycling. More importantly, the SC structure could suppress nearly 50 % of internal strain, prodigiously reducing the local stress accumulation accompanied by the inhomogeneous sodium concentration gradient during the charging/discharging processes. The smaller the stress accumulation, the more stable the crystal structure would be obtained, which maintained a more superb mechanical stability of the SC cathode material. At the same time, a high-spin state of Fe in the SC sample was confirmed by both of electron paramagnetic resonance and temperature-dependent magnetization susceptibility, indicating that the eg orbital occupation of Fe2+ could be regulated to optimize the bond strength between the reduction and oxidation processes. As a consequence, the band gap of SC material has decreased from 1.66 to 1.45 eV, and the electronic conductivity has increased from 6.0 to 32.4 μS/cm. It is believed that the SC cathode material could be a competitive candidate material for sodium ion batteries.

Diffusiophoresis of a Charged Soft Sphere in a Charged Spherical Cavity

The quasi-steady diffusiophoresis of a soft particle composed of an uncharged hard sphere core and a uniformly charged porous surface layer in a concentric charged spherical cavity full of a symmetric electrolyte solution with a concentration gradient is analyzed. By using a regular perturbation method with small fixed charge densities of the soft particle and cavity wall, the linearized electrokinetic equations relevant to the fluid velocity field, electric potential profile, and ionic concentration distributions are solved. A closed-form formula for the diffusiophoretic (electrophoretic and chemiphoretic) velocity of the soft particle is obtained as a function of the ratios of the core-to-particle radii, particle-to-cavity radii, particle radius to the Debye screening length, and particle radius to the permeation length in the porous layer. In typical cases, the confining charged cavity wall significantly influences the diffusiophoresis of the soft particle. The fluid flow caused by the diffusioosmosis (electroosmosis and chemiosmosis) along the cavity wall can considerably change the diffusiophoretic velocity of the particle and even reverse its direction. In general, the diffusiophoretic velocity decreases with increasing core-to-particle radius ratios, particle-to-cavity radius ratios, and the ratio of the particle radius to the permeation length in the porous layer, but increases with increasing ratios of the particle radius to the Debye length.

Boosting interface compatibility of high-voltage LiNi0.5Mn1.5O4 cathode materials with an ionic-conductive Li0.33La0.56TiO3 coating

High voltage LiNi0.5Mn1.5O4 (LNMO) is a crucial cathode material for lithium-ion batteries (LIBs) aiming at high energy densities. However, its performance is hindered by the dissolution of transition metal ions and the instability of the cathode electrolyte interface (CEI) film at elevated voltages. To address these issues, we report a solvothermal method to prepare LNMO coated with Li+-conductor Li0.33La0.56TiO3 (LNMO@LLTO). Our study reveals that the LLTO coating not only enhances ion diffusion at the interface, minimizing the Li+ concentration gradient, and acts as a barrier against Mn-ion dissolution. This coating minimizes side reactions, mitigates structural degradation, and promotes the formation of a stable and balanced CEI film that incorporates LLTO, thus ensuring the long-term cycle stability. When compared to bulk LNMO, the LNMO@LLTO cathode demonstrates superior performance, maintaining reversible capacities of 111.4 and 102.2 mAh·g−1 after 500 cycles at 2 and 5C at 25 °C, respectively. Even at 60 °C, the LNMO@LLTO maintains a high capacity of 94.3 mAh·g−1 with minimal electrochemical polarization after 200 cycles at 2C. This simple preparation technique, together with its performance promotion, offers new insights into the development of high voltage cathode materials for high energy density LIBs.

Mapping the membrane orientation of auxin homeostasis regulators PIN5 and PIN8 in Arabidopsis thaliana root cells reveals their divergent topology.

PIN proteins establish the auxin concentration gradient, which coordinates plant growth. PIN1-4 and 7 localized at the plasma membrane (PM) and facilitate polar auxin transport while the endoplasmic reticulum (ER) localized PIN5 and PIN8 maintain the intracellular auxin homeostasis. Although an antagonistic activity of PIN5 and PIN8 proteins in regulating the intracellular auxin homeostasis and other developmental events have been reported, the membrane topology of these proteins, which might be a basis for their antagonistic function, is poorly understood. In this study we optimized digitonin based PM-permeabilizing protocols coupled with immunocytochemistry labeling to map the membrane topology of PIN5 and PIN8 in Arabidopsis thaliana root cells. Our results indicate that, except for the similarities in the orientation of the N-terminus, PIN5 and PIN8 have an opposite orientation of the central hydrophilic loop and the C-terminus, as well as an unequal number of transmembrane domains (TMDs). PIN8 has ten TMDs with groups of five alpha-helices separated by the central hydrophilic loop (HL) residing in the ER lumen, and its N- and C-terminals are positioned in the cytoplasm. However, the topology of PIN5 comprises nine TMDs. Its N-terminal end and the central HL face the cytoplasm while its C-terminus resides in the ER lumen. Overall, this study shows that PIN5 and PIN8 proteins have a divergent membrane topology while introducing a toolkit of methods for studying membrane topology of integral proteins including those localized at the ER membrane.

Migration behavior of iron and phosphorus during gas-based reduction for high-phosphorus iron ore

With the depletion of high-grade iron ore, it is necessary to develop low-quality high-phosphorus iron ore through economical and sustainable solutions. In this study, we presented simultaneous enrichment of iron (Fe) and phosphorus (P) to recover P from high-phosphorus iron ore and clarified the migration of P from the original apatite to reduced iron during the direct reduction process. To capture the migration route, gas-based reduction at a relatively slow rate was conducted on two typical iron ores samples (low-grade and high-grade) at different temperatures and times. Results indicate that there are concentration gradients for P and Fe of reaction products in the low-grade iron ore at 1400 °C. The P content continuously increased in the sequence from metallic iron (Fe), wustite (FeO), and fayalite (Fe2SiO4), to apatite (Ca3(PO4)3F). Conversely, the content of Fe gradually decreased. During this process, P dissolved from apatite entered and formed P-bearing fayalite. For the high-grade iron ore, P-bearing fayalite with a metastable structure disappeared as the reduction progressed, and P was released and then reduced to a gaseous state, finally absorbed by metallic iron. Furthermore, when metallic iron was not formed in the initial 60 min at 1300 °C, the P migrated from the apatite to the fayalite and gas phase. As the reduction time increased from 60 min to 240 min, the formed metallic iron provided a site for gasified P, which inhibited the volatilization of P and contributed to Fe and P enrichment.

Capacitive deionization technology with multi-stage treatment as an efficient desalination process for agricultural irrigation

Novel capacitive deionization (CDI) technology is recognized as a cheap desalination method and holds a promise to be deployed in low-profit fields such as agricultural and municipal works. In this study, the application feasibility of CDI technology in agricultural irrigation is thoroughly investigated. The desalination performance of three operation methods (“low flow rate”, “high applied voltage”, and “two-stage treatment”) are compared for treating artificial brackish water of 2000 mg L−1 to a set desalination target (600 mg L−1). Among these three methods, “two-stage treatment” overwhelms the other two methods regarding several desalination indicators, achieving a decent productivity (1.5 L h−1 m−2) with a small energy input of 1.4 kWh m−3. The modified Donnan model indicates that energy dissipation is mitigated in a high flow rate adopted in two-stage treatment, and meantime a high desalination capacity and a good charge efficiency are achieved. In addition, desalinated water with a salt concentration gradient is produced by the CDI module for tomato seedlings irrigation. Compared with the tomato seedlings irrigated by feedwater (2000 mg L−1), the total length and the biomass weight of those irrigated by desalinated water of 300 mg L−1 increase 51.1 % and 119.8 %, respectively. The research accomplishes a proof-of-concept of the agricultural application of CDI technology, and provides reliable data as the foundation for its future practical operation.

Atmospheric Pressure Enhanced Self-Sealing Rotation-SlipChip with Programmable Concentration Gradient Generation for Microbiological Applications.

In microbiological research, traditional methods for bacterial screening and antibiotic susceptibility testing are resource-intensive. Microfluidics offers an efficient alternative with rapid results and minimal sample consumption, but the demand for cost-effective, user-friendly platforms persists in communities and hospitals. Inspired by the Magdeburg hemispheres, the strategy adapts to local conditions, leveraging omnipresent atmospheric pressure for self-sealing of Rotation-SlipChip (RSC) equipped with a 3D circular Christmas tree-like microfluidic concentration gradient generator. This innovative approach provides an accessible and adaptable platform for microbiological research and testing in diverse settings. The RSC can avoid leakage concerns during multiple concentration gradient generation, chip-rotating, and final long-term incubation reaction (≥24h). Furtherly, RSC subtypes adapted to different reactions can be fabricated in less than 15min with cost less than $1, the result can be read through designated observational windows by naked-eye. Moreover, the RSC demonstrates its capability for evaluating bacterial biomarker activity, enabling the rapid assessment of β-galactosidase concentration and enzyme activity within 30min, and the limit of detection can be reduced by 10-fold. It also rapidly determines the minimum antibiotic inhibitory concentration and antibiotic combined medications results within 4 h. Overall, these low-cost and user-friendly RSC make them invaluable tools in determinations at previously impractical environment.

Teasing out the Effects of Natural Stressors at Chemically Contaminated Sites.

Aquatic ecosystems are often impacted by a multitude of stressors, many of which are introduced by a combination of anthropogenic activities such as agricultural development, urbanization, damming, and industrial discharge. Determining the primary stressors responsible for ecological impairments at a site can be complex and challenging; however, it is crucial for making informed management decisions. Improper diagnosis of an impaired system can lead to misguided attempts at remediation, which can be both time consuming and costly. We focused on the development, implementation, and evaluation of methodologies that, in combination, allowed us to identify the primary stressors. These included a four-phase, weight-of-evidence (WOE) assessment including in situ Toxicity Identification and Evaluation (iTIE) testing, physicochemical and macrobenthos characterization, reciprocal sediment transplants, and laboratory and in situ toxicity testing. The contaminants of concern (COCs) at the site were elevated levels of ammonia, chloride, pH, and total dissolved solids in groundwater upwellings into a high-quality waterway. Reciprocal transplants of site sediments and nearby reference sediments and traditional benthic sampling showed impaired benthic indices and multiple stations around a contaminated industrial settling basin. Impaired stations had elevated COCs in groundwaters but exhibited a steep vertical concentration gradient, with concentrations decreasing near the sediment-surface water interface. We describe Phase 4 of the study, which focused on teasing out the role of dissolved oxygen sags in benthic macroinvertebrate responses. Extensive submerged and emergent macrophytes, algae, and cyanobacteria co-occurred at the impaired sites and increased throughout the summer. Laboratory testing suggested that ammonia and pH were possibly toxic at the sites, based on groundwater concentrations. The in situ toxicity testing, however, showed toxicity occurring even at stations with low levels of COCs concurrently with large diurnal fluxes in dissolved oxygen (DO). A final phase using a type of iTIE approach utilized limnocorrals with and without aeration and with in situ toxicity measures using Hyalella azteca. The Phase 4 assessment revealed that low DO levels were primarily responsible for impaired benthic communities, and COC upwellings were diluted at the sediment-water interface to nontoxic levels. These findings will allow for improved management decisions for more efficient and effective restoration activities. Environ Toxicol Chem 2024;43:1524-1536. © 2024 SETAC.

High temperature and nib acidification during cacao-controlled fermentation improve cadmium transfer from nibs to testa and the liquor’s flavor

Migration of nib Cd to the testa during fermentation can be achieved with high temperatures (> 45 °C) and low nib pH values (< 5.0) using spontaneous fermentation. However, this low pH can lead to low flavor quality. This study used three controlled temperature fermentation treatments on three cacao genotypes (CCN 51, ICS 95, and TCS 01) to test its effects on the nib pH, the migration of nib Cd to the testa, and the liquor flavor quality. All treatments were effective in reducing the total nib Cd concentration. Nevertheless, the treatment with the higher mean temperature (44.25 °C) and acidification (pH 4.66) reached the highest mean nib Cd reductions throughout fermentation, a 1.37 factor in TCS 01, promoting the development of fine-flavor cocoa sensorial notes. In unfermented beans, the Cd concentration of nibs was higher than that of the testa, and the Cd migration proceeded down the total concentration gradient. However, Cd migration was observed against the concentration gradient (testa Cd > nib Cd) from the fourth day. Cd migration could increase by extensive fermentation until the sixth day in high temperatures and probably by the adsorbent capacity of the testa. Genotype-by-treatment interactions were present for the nib Cd reduction, and a universal percentage of decrease of Cd for each genotype with fermentation cannot be expected. Selecting genotypes with highly adsorbent testa combined with controlled temperatures would help reduce the Cd concentration in the cacao raw material, improving its safety and quality.

Impact of variable viscosity, thermal conductivity, and Soret–Dufour effects on MHD radiative heat transfer in thin reactive liquid films past an unsteady permeable expandable sheet

AbstractSignificance of magnetohydrodynamic effect on a viscous (temperature‐dependent) and chemically reactive thin fluid film flow past an unsteady permeable stretchable plate with Soret–Dufour effects, nonlinear thermal radiative, and suction under the action of a convective type of boundary condition is analyzed. The problem consists of nonlinear governing basic equations that are highly nonlinear due to the existence of nonlinear thermal radiative terms in the energy equation. Analytical solutions are challenging to achieve for such types of problems, so a numerical scheme adopts the numerical solution. Computed solutions indicate that decreasing the Dufour number (and simultaneously increasing the Soret number) enhances heat flux, whereas the reverse trend is estimated for the concentration gradient field. The influence of magnetization indicates a decrement in the thin liquid film velocity distribution, whereas an increment is observed in temperature and solutal gradient profiles. Further, an enhancement in thermoradiative values focuses on decreasing the heat flux profiles, whereas a decreasing trend is determined in the solutal gradient by incrementing the Schmidt number. The variations of the velocity field, temperature, and concentration gradients are shown for the unsteady parameter lying in the range [0.8, 1.4]. Similarly, the range of different parameters utilized are [0.0, 1.0], [0.0, 2.0], [0.8, 1.5], [0.5, 2.0], [0.0, 1.0], [0.2, 3.0], [1.0, 2.0], [0.0, 3.0], [0.4, 1.0], and [0.4, 1.0]. The novelty of the present study lies in its analysis of complex fluid dynamics phenomena and their implications for various industrial processes and engineering applications, including coating processes, heat exchangers, microfluidics, and biomedical engineering. The insights gained from the study can contribute to developing more efficient and innovative research in these areas. Further, we have compared the present results with those available in the literature under some special cases and found them to be in excellent agreement.

Toxicology of milrinone by zebrafish embryotoxicity test.

Milrinone, a phosphodiesterase III inhibitor with contractile and vasodilatory effects, is widely used in acute decompensated heart failure and medically refractory end-stage heart failure (HF). The adverse reactions of milrinone have been extensively explored clinically, but its possible toxicities and underlying molecular mechanisms in embryo development need further understanding as its clinical applications increase. Herein, we assessed the milrinone toxicity using the zebrafish embryotoxicity test (ZET), with a view of providing evidence and guidancefor gravidas medicine. We carried out ZET by exposing embryos to a milrinone culture with a series concentration gradients since 1.5 hours post fertilization (hpf) and observed and assessed mortality and hatching rates of drug-treated zebrafishes at 24, 48, 72, and 96 hpf. No significant lethal effect was found in milrinone-treated zebrafish, but hatching rate of eggs at 48 hpf was up-regulated with the increase of milrinone concentration. The impact of milrinone on embryogenesis was assessed through body length, eye area, yolk sac area, swim bladder inflation area, pericardial area and venous congestion area at 96hpf. 150 μg/mL or higher milrinone treatment showed significant effects in the indicators. Organ disorders including enlarged pericardium, liver atrophy and decreased blood vessels were observed in dysplasia individuals versus controls. TUNEL assay suggested the ability of milrinone to induce apoptosis in malformation embryos. Quantitative real-time PCR showed aberrant expressions of transcription factors associated with heartdevelopment and genes related to liver development and apoptosis regulation. Therefore, ZET is feasible for the milrinone toxicity test, and high-dose milrinone causes harm to the embryonic development of zebrafish, especially in embryonic carcinogenesis, vasculogenesis, and hepatogenesis.

Removal of total ammoniacal nitrogen from reject water through selective electrodialysis reversal and bipolar electrodialysis

The removal of ammonium and ammonia, represented as total ammoniacal nitrogen (TAN), from reject water through electro-dialysis (ED) and bipolar membrane electrodialysis (BPMED) encounters challenges such as organic fouling, NH3 back-diffusion, and high energy consumption. The efficacy of electrodialysis reversal (EDR) combined with bipolar membrane electrodialysis using cation-exchange membranes (BPC) was assessed as a more practical configuration (EDR + BPC). Additionally, a novel configuration involving monovalent selective cation-exchange membranes (MSCEMs) in an EDR + BPC setup (SEDR + BPC) was investigated. Comparisons were made among BPMED, EDR + BPC, and SEDR + BPC under three load ratios (LN) of 0.8, 1, and 1.3 during continuous operation. The innovative SEDR + BPC configuration, with an LN of 0.8, exhibited the lowest energy consumption for transported TAN (ETAN) at 4.4 MJ·kgN−1 removal and achieved the highest TAN removal efficiency of 78 % with an LN of 1.3. In contrast to conventional BPMED, SEDR + BPC allowed for the recovery of potentially back-diffused NH3 into the acid chamber, minimizing transport losses. Furthermore, scaling in the base chamber was reduced due to the contribution of MSCEMs when applying an LN of 0.8. The MSCEMs increased the molar ratio of TAN over (Mg2+ + Ca2+) in the concentrate and decreased it in the diluate. EDR + BPC and SEDR + BPC configurations exhibited stable and lower cell resistance throughout the operation compared to BPMED, attributed to their ability to generate higher concentration gradients. The results clearly demonstrated the feasibility of low-energy TAN removal from real reject water from sludge anaerobic digestion using the SEDR + BPC setup.

Reduction of Taylor dispersion in a capillary by spin-up flow—Theoretical insights

We have developed a theoretical framework to characterize the transport and mixing of a passive scalar in a capillary tube. In this configuration, a suspension of magnetic nanoparticles undergoes Poiseuille flow, while a rotating magnetic field is applied around the tube’s revolution axis, inducing a secondary flow in the azimuthal direction. This secondary flow facilitates the mitigation of concentration gradients and radial dispersion associated with the axial parabolic Poiseuille profile. The improvement in mixing is emphasized by a new dimensionless parameter, the mixing factor, which is incorporated into the scalar transport equation. Such a factor acts as a quantitative measure of the effect of the tangential motion induced by the spin-up flow on the overall mixing efficiency of the liquid and the observed reduction of the Taylor dispersion in the measured residence time distributions. Recognizing the mixing factor as a crucial parameter advances our understanding of the mechanisms governing scalar transport and provides a valuable tool for predicting and optimizing mixing in laminar capillary flows subjected to spin-up motion.

Effects of stress relief annealing in NGO steels

The effect of stress relief annealing (SRA) has been investigated on two classes of non-grain oriented (NGO) steels and with different sheet thickness. Magnetic properties were measured on mechanically sheared and water jet cut Epstein strips before and after SRA treatment at 800 °C in a nitrogen gas atmosphere. Significant improvement in power loss was achieved for the steel with lower aluminium content after SRA but the effect was much smaller for steel with the higher aluminium level, especially for thinner sheets where the SRA treatment was actually deleterious. No change in steel chemistry after SRA was found that could explain these differences. Microstructural examination showed residual dislocation substructures due to shearing before SRA and recrystallisation along the sheared edges together with recovery of the dislocation structures afterwards.A completely new finding was the presence of dislocation loops after SRA in the steel with higher aluminium content. These were not present previously but were created during the heat treatment. The presence of these dislocation loops is proposed as the reason for the weak or adverse effect of SRA on power loss. Detailed electron microscopy revealed that there are two families of dislocation loops having either Burgers’ vectors of a 〈100〉 lying on {100} planes or a√3/2 〈111〉 on {111 planes}. A model is presented whereby oxidation which occurs at the sheet surfaces causes a concentration gradient within which the Al atoms diffuse. This process necessitates a balancing flux of vacancies diffusing into the interior. When the content of vacancies exceeds the equilibrium content they agglomerate and ‘precipitate’ out as vacancy dislocation loops.

Net escape velocity, transfer probability, and travel time distributions within a cross-ventilated room model sheltered by urban-like block array

Natural ventilation offers significant advantages, especially in terms of energy conservation. However, most published articles have focused on the ventilation flow rate to determine the average contaminant concentration, while few have examined local ventilation distributions. Therefore, isothermal steady-state Reynolds-averaged Navier–Stokes simulations were conducted to analyze the airflow and scalar concentration fields of a cross-ventilation model sheltered by buildings. Based on these fields, we generated the spatial distributions of ventilation indices, namely, the net escape velocity (NEV), point-to-point indices transfer probability (TP), and travel time (TT), to discuss the dispersion of scalars emitted from local points in a room with natural ventilation. The NEV, which indicates the direction of the scalar discharge from each cell, exhibited a distribution distinct from the advection velocity because of concentration gradient effect. Higher TPs were observed when evaluated from a contaminant source to a target point following the NEV streamlines. Meanwhile, lower TTs were observed when evaluated in a point near the source and also from a contaminant source to a target point following the NEV streamlines. Although TP and TT are independent ventilation indices, a negative correlation between them was observed. Instead of the ventilation flow rate, the detailed structure of scalar dispersion can now be described by simultaneously analyzing the ventilation efficiency indices, which provide information on the general contaminant transport direction, and the probability and duration of transfer from a source to a target point. This potentially helps in the design of ventilation system especially in room lay-out to avoid cross-contamination.