Nonuniform Collective Dissolution of Bubbles in Regular Pore Networks

Understanding the evolution of solute concentration gradients underpins the prediction of porous media processes limited by mass transfer. Here, we present the development of a mathematical model that describes the dissolution of spherical bubbles in two-dimensional regular pore networks. The model is solved numerically for lattices with up to 169 bubbles by evaluating the role of pore network connectivity, vacant lattice sites and the initial bubble size distribution. In dense lattices, diffusive shielding prolongs the average dissolution time of the lattice, and the strength of the phenomenon depends on the network connectivity. The extension of the final dissolution time relative to the unbounded (bulk) case follows the power-law function, $${B^k/\ell }$$ B k / ℓ , where the constant $$\ell$$ ℓ is the inter-bubble spacing, B is the number of bubbles, and the exponent k depends on the network connectivity. The solute concentration field is both the consequence and a factor affecting bubble dissolution or growth. The geometry of the pore network perturbs the inward propagation of the dissolution front and can generate vacant sites within the bubble lattice. This effect is enhanced by increasing the lattice size and decreasing the network connectivity, yielding strongly nonuniform solute concentration fields. Sparse bubble lattices experience decreased collective effects, but they feature a more complex evolution, because the solute concentration field is nonuniform from the outset.

Versatile and Targeted Validation of Space-Borne XCO2, XCH4 and XCO Observations by Mobile Ground-Based Direct-Sun Spectrometers

Satellite measurements of the atmospheric concentrations of carbon dioxide (CO2), methane (CH4) and carbon monoxide (CO) require careful validation. In particular for the greenhouse gases CO2 and CH4, concentration gradients are minute challenging the ultimate goal to quantify and monitor anthropogenic emissions and natural surface-atmosphere fluxes. The upcoming European Copernicus Carbon Monitoring mission (CO2M) will focus on anthropogenic CO2 emissions, but it will also be able to measure CH4. There are other missions such as the Sentinel-5 Precursor and the Sentinel-5 series that target CO which helps attribute the CO2 and CH4 variations to specific processes. Here, we review the capabilities and use cases of a mobile ground-based sun-viewing spectrometer of the type EM27/SUN. We showcase the performance of the mobile system for measuring the column-average dry-air mole fractions of CO2 (XCO2), CH4 (XCH4) and CO (XCO) during a recent deployment (Feb./Mar. 2021) in the vicinity of Japan on research vessel Mirai which adds to our previous campaigns on ships and road vehicles. The mobile EM27/SUN has the potential to contribute to the validation of 1) continental-scale background gradients along major ship routes on the open ocean, 2) regional-scale gradients due to continental outflow across the coast line, 3) urban or other localized emissions as mobile part of a regional network and 4) emissions from point sources. Thus, operationalizing the mobile EM27/SUN along these use cases can be a valuable asset to the validation activities for CO2M, in particular, and for various upcoming satellite missions in general.

Reaction-free concentration gradient generation in spatially non-uniform AC electric fields

The ability to generate stable, spatiotemporally controllable concentration gradients is critical for both electrokinetic and biological applications such as directional wetting and chemotaxis. Electrochemical techniques for generating solution and surface gradients display benefits such as simplicity, controllability, and compatibility with automation. Here, we present an exploratory study for generating micro-scale spatiotemporally controllable gradients using a reaction-free electrokinetic technique in a microfluidic environment. Methanol solutions with ionic Fluorescein isothiocyanate (FITC) molecules were used as an illustrative electrolyte. Spatially non-uniform alternating current (AC) electric fields were applied using hafnium dioxide (HfO2) coated Ti/Au electrode pairs. Results from spatial and temporal analysis, along with control experiments suggest that the FITC ion concentration gradient in bulk fluid (over 50 µm from the electrode) was established due to spatial variation of electric field density, and was independent of electrochemical reactions at the electrode surface. The established ion concentration gradients depended on both amplitudes and the frequencies of the oscillating AC electric field. Overall, this work reports a novel approach for generating stable and spatiotemporally tunable gradients in a microfluidic chamber using a reaction-free electrochemical methodology.

Reaction-free concentration gradient generation in spatially non-uniform AC electric fields

The ability to generate stable, spatiotemporally controllable concentration gradients is critical for both electrokinetic and biological applications such as directional wetting and chemotaxis. Electrochemical techniques for generating solution and surface gradients display benefits such as simplicity, controllability, and compatibility with automation. Here, we present an exploratory study for generating micro-scale spatiotemporally controllable gradients using a reaction-free electrokinetic technique in a microfluidic environment. Methanol solutions with ionic Fluorescein isothiocyanate (FITC) molecules were used as an illustrative electrolyte. Spatially non-uniform alternating current (AC) electric fields were applied using hafnium dioxide (HfO2) coated Ti/Au electrode pairs. Results from spatial and temporal analysis, along with control experiments suggest that the FITC ion concentration gradient in bulk fluid (over 50 µm from the electrode) was established due to spatial variation of electric field density, and was independent of electrochemical reactions at the electrode surface. The established ion concentration gradients depended on both amplitudes and the frequencies of the oscillating AC electric field. Overall, this work reports a novel approach for generating stable and spatiotemporally tunable gradients in a microfluidic chamber using a reaction-free electrochemical methodology.

Влияние ионной подсистемы на термоэлектрический эффект в коллоидных растворах

The thermoelectric effect is investigated in mixtures of colloidal solutions with ionic electrolytes in the initial state, when the formation of concentration gradients under the influence of an inhomogeneous temperature field can be neglected. Based on experimental measurements in mixtures with different concentrations of colloidal particles and ions, the conditions under with the coefficient of thermoelectric EMF is determined by the ion subsystem and under which the main contribution to the value of the thermoelectric force is made by colloidal particles are determined.

Generation of Concentration Gradients by a Outer-Circumference-Driven On-Chip Mixer

The concentration control of reagents is an important factor in microfluidic devices for cell cultivation and chemical mixing, but it is difficult to realize owing to the characteristics of microfluidic devices. We developed a microfluidic device that can generate concentration gradients among multiple main chambers. Multiple main chambers are connected in parallel to the body channel via the neck channel. The main chamber is subjected to a volume change through a driving chamber that surrounds the main chamber, and agitation is performed on the basis of the inequality of flow caused by expansion or contraction. The neck channel is connected tangentially to the main chamber. When the main chamber expands or contracts, the flow in the main chamber is unequal, and a net vortex is generated. The liquid moving back and forth in the neck channel gradually absorbs the liquid in the body channel into the main chamber. As the concentration in the main chamber changes depending on the pressure applied to the driving chamber, we generated a concentration gradient by arranging chambers along the pressure gradient. This allowed for us to create an environment with different concentrations on a single microchip, which is expected to improve observation efficiency and save space.

Hydrodynamic flow and concentration gradients in the gut enhance neutral bacterial diversity

The gut microbiota features important genetic diversity, and the specific spatial features of the gut may shape evolution within this environment. We investigate the fixation probability of neutral bacterial mutants within a minimal model of the gut that includes hydrodynamic flow and resulting gradients of food and bacterial concentrations. We find that this fixation probability is substantially increased, compared with an equivalent well-mixed system, in the regime where the profiles of food and bacterial concentration are strongly spatially dependent. Fixation probability then becomes independent of total population size. We show that our results can be rationalized by introducing an active population, which consists of those bacteria that are actively consuming food and dividing. The active population size yields an effective population size for neutral mutant fixation probability in the gut.

The Effects of Concentration Gradient of Nitrogen Compounds on the Ammonium-nitrogen and Nitrate-nitrogen Fluxes at Sediment-Water Interface

The incubation experiments focused on altering concentration gradients of nitrogen between sediment and overlying water to examine the diffusion flux of ammonium-nitrogen (NH4+) and nitrate-nitrogen (NO3-) at sediment-water interface. In this study, the diffusion flux can be estimated based on calculating the average of the net change rate of nutrient concentrations in the overlying water. For the incubation experiment of different TN concentrations in the sediment, the results showed that the diffusion flux of ammonia at sediment-water interface is -52.57~84.57 mg·m-2·d-1, and for nitrate diffusion flux, the changing range during the incubation experiment is -110.13~143.25 mg·m-2·d-1. For the incubation experiment of different nitrogen concentrations in the overlying water, the results of NH4+-N diffusion flux in L, M, H treatment were 3.37, -4.94, -3.84 mg·m-2·d-1, respectively. And the average diffusion flux of nitrate in L (0 mg NO3--N, 0 mg NH4+-N), M (0.5 mg NO3--N, 1.5 mg NH4+-N) and H (1 mg NO3--N, 2.5 mg NH4+-N) treatment were 12.30, 10.39 and 7.11 mg·m-2·d-1. Results highlighted that concentrations gradient of nutrients were indeed an important factor affecting the diffusion flux at sediment-water interface. In addition, the diffusion of nutrients at sediment-water interface in aquatic ecosystem is not only controlled by concentration gradients, some other factors such as incoming water, hydrodynamics, dissolved oxygen content, sediment structure, biological disturbance, horizontal migration and diffusion of nutrients and turbulent diffusion caused by wind and wave, are equally important.

The Effect of Flux Dysconnectivity Functions on Concentration Gradients Changes in a Multicomponent Model of Convectional Reaction-Diffusion by the Example of a Neurovascular Unit

A convectional diffusion of nutrients around the blood vessels in brain occurs in well-structured neurovascular units (NVU) including neurons, glia and micro vessels. A common feature of the process is a combination of a relatively high-speed delivery solution stream inside the blood vessel and a low-speed convectional flow in parenchyma. The specific trait of NVU is the existence of a tight cover layer around the vessels which is formed by shoots (end-feet) of astrocytes. This layer forms so called blood-brain barrier (BBB). Under different pathological states the permeability of BBB is changed. The concentration gradient of a chemical compound in NVU has been modelled using a combination of mathematical description of a cerebral blood flow (CBF) and further 3D diffusion away from the blood vessels borders. The governing equation for the blood flow is the non-steady-state Navier–Stokes equation for an incompressible non-Newtonian fluid flow without buoyancy effects. BBB is modeled by the flux dysconnectivity functions. The velocity of fluid flow in the paravascular space was estimated using Darcy's law. Finally, the diffusion of the nutrient is considered as a convectional reaction-diffusion in a porous media. By the example of glucose, it was shown that increased permeability of BBB yields an increased level of the nutrient even under essential (on 70%) decrease of CBF. Contrarily, a low BBB permeability breeds a decreased concentration level under increased (on 50%) CBF. Such a phenomenon is explained by a smooth enlarge of the direct diffusion area for a blood-to-brain border glucose transport having three-level organization.