Agarose is known to form a homogeneous thermoreversible gel in an aqueous medium over a critical polymer concentration. The solid-liquid phase transitions are thermoreversible but depend on the molecular structure of the agarose sample tested. The literature has mentioned that agarose gels could remain stable in non-solvents such as acetone or ethanol. However, there has been no characterization of their behavior nor a comparison with the gels formed in a good solvent such as water. In the first step of this article, the structure was characterized using ¹H and ¹³C NMR in both D₂O and DMSO-d6 solvents. DMSO is a solvent that dissolves agarose regardless of the temperature. First, we have determined a low yield of methyl substitution on the D-galactose unit. Then, the evolution of the ¹H NMR spectrum was monitored as a function of temperature during both increasing and decreasing temperature processes, ranging from 25 to 80 °C. A large thermal hysteresis was obtained and discussed, which aided in the interpretation of rheological behavior. The hysteresis of NMR signals is related to the mobility of the agarose chains, which follows the sol/gel transition depending on the chains’ association with H-bonds between water and the -OH groups of agarose for tightly bound water and agarose/agarose in chain packing. In the second step of the study, the water in the agarose gel was exchanged with ethanol, which is a non-solvent for agarose. The resulting gel was stable, and its properties were characterized using rheology and compared to its behavior in aqueous media. The bound water molecules that act as plasticizers were likely removed during the exchange process, resulting in a stronger and more brittle gel in ethanol, with higher thermal stability compared to the aqueous gel. It is the first time that such gel is characterized without phase transition when passing from a good solvent to a non-solvent. This extends the domains of application of agarose.

In this work, the influence of nozzle shape on microfluidic ink jet breakup is investigated. First, an industrial ink used in continuous inkjet (CIJ) printing devices is selected. Ink rheological properties are measured to ensure an apparent Newtonian behavior and a constant surface tension. Then, breakup lengths and shapes are observed on a wide range of disturbance amplitude for four different nozzles. Later on, ink breakup behaviors are compared to the linear theory. Finally, these results are discussed using numerical simulations to highlight the influence of the velocity profiles at the nozzle outlet. Using such computations, a simple approach is derived to accurately predict the breakup length for industrial CIJ nozzles.

The theory of the so-called Rayleigh–Plateau instability of fluid jets has been widely studied and can be used to predict the breakup length of liquid jets. Recently, in the work of Rosello et al. [J. Fluids Eng. 140(3), 031202 (2018)], the linear theory was enhanced to accurately predict the breakup length of continuous ink jets of Newtonian fluids by accounting for the influence of the nozzle geometry. In the present work, the influence of a shear-thinning behavior is addressed for both the breakup morphologies and breakup lengths in a linear regime. A comparison with the experimental data shows an excellent agreement extending the model of Rosello et al. to a non-Newtonian shear-thinning fluid.

The Rayleigh-Plateau instability, a phenomenon of paramount significance in fluid dynamics, finds widespread application in the Continuous InkJet (CIJ) printing process. This study presents a comprehensive dataset comprising experimental investigations of fluid jet breakup phenomena under large-amplitude stimulation conditions using an industrial CIJ print-head from Markem-Imaje. Unlike previous studies, this dataset encompasses a diverse range of experimental conditions, including nine different Newtonian fluids with meticulously measured rheological properties (viscosities, surface tensions and densities). The applied stimulation amplitudes vary from 5V to 45V, representing a substantial span of excitation levels.

Blood rheology and microcirculation are strongly influenced by red blood cell (RBC) aggregation. The aggregability of RBCs can vary significantly due to factors such as their mechanical and membrane surface properties, which are affected by cell aging in vivo. In this study, we investigate RBC aggregability as a function of their density, a marker of cell age and mechanical properties, by separating RBCs from healthy donors into different density fractions using Percoll density gradient centrifugation. We examine the dissociation rates of aggregates in a controlled medium supplemented with Dextran, employing an extensional flow technique based on hyperbolic microfluidic constrictions and image analysis, assisted by a convolutional neural network (CNN). In contrast to other techniques, our microfluidic experimental approach highlights the behavior of RBC aggregates in dynamic flow conditions relevant to microcirculation. Our results demonstrate that aggregate dissociation is strongly correlated with cell density and that aggregates formed from the denser fractions of RBCs are significantly more robust than those from the average cell population. This study provides insight into the effect of RBC aging in vivo on their mechanical properties and aggregability, underscoring the importance of further exploration of RBC aggregation in the context of cellular senescence and its potential implications for hemodynamics. Additionally, it suggests that this technique can complement existing methods for improved evaluation of RBC aggregability in health and disease.