Abstract The microstructure of the aqueous solutions of purified acidic Sophorolipid (SL) has previously been studied using highly sophisticated methods such as SANS and Cryo-TEM. We were interested in whether (a) the main findings also apply to commercially available SL (which is a mixture of acidic and lactonic SL) and (b) more readily available methods such as DLS can be used to gain insight into the molecular aggregation of SL. Our work was motivated by the increasing interest in biosurfactants for applications in personal and household care. Moreover, the origin behind the more or less lack of rheological response to changes in pH is of practical relevance, as it is somewhat unusual for a carboxylate-group containing surfactant. By using DLS microrheology, we could elucidate the aggregation structure and dynamics of the surfactant on a microscopic scale. Surprisingly, the different degrees of protonation only impacted the microscopic properties such as exchange kinetics and the plateau values of the storage moduli.

Abstract Catalytic conversion of fructose to levulinic and formic acids over tin-containing superacid (H0 = −14.52) mixed oxide was studied. Mesoporous ZrO2–SiO2–SnO2 (Zr:Si:Sn = 1:2:0.4) was synthesized by the sol–gel method. The fructose transformation was carried out in a rotated autoclave at 160–190 ◦C for 1–5 h using a 20 wt.% aqueous solution. The results showed that doping ZrO2–SiO2 samples with Sn4+ ions improved both fructose conversion and selectivity toward levulinic and formic acids. Under optimal conditions of 180 ◦C, 3.5 h and fructose to catalyst weight ratio 20:1,levulinic and formic acids yields were 80% and 90%, respectively, at complete fructose conversion. At this, humic substances formed in the quantity of 10 wt.% based on the target products.

Abstract The micro-scale morphology of the receding contact line of dilute polyethylene oxide solution drops (c∼100 ppm) after impact and inertial spreading on a fluorinated hydrophobic surface is investigated. One can observe the formation of transient liquid filaments and dendritic structures that evolve into a bead-on-a-string structure similar to the well-known capillary breakup mechanism of dilute polymer solutions, which confirm the interaction between stetched polymer coils and the receding three-phase contact line. The estimation of the average polymer force per unit contact line lenght provides a quantitative explanation for the reduction of the contact line retraction velocity reduction observed experimentally.

Abstract Thin films of chitosan are often deposited on various surfaces to provide them with antiseptic properties. In the presented research, chitosan foils were obtained using two methodsand treated with nitrogen plasma. The obtained materials were characterized by measuring the wettability of the test liquids, and the apparent surface free energy was calculated using the Tadmor equilibrium contact angles. The surface topography was characterized using optical profilometry and SEM. On the other hand, the effect of plasma on surface groups was investigated using the FTIR-ATR technique. Plasma activation of the surface increases the polarity of the surface. This is observed in the changed surface roughness and the share of functional groups on the surface.

Abstract Polymers containing magnetic properties play an important role in biomedical therapies, such as embolotherapy or hyperthermia, for their differentiated properties. In this work, magnetite (Fe3O4) nanoparticles were synthesized by the coprecipitation method and dispersed into a thermoplastic matrix of poly(vinyl pivalate) through an emulsion polymerization process. The main goal was the individual encapsulation of magnetite nanoparticles to improve the magnetic response of the magneto-polymeric materials using polymerizable carboxylic acids as coating agents, minimizing the leaching of nanoparticles throughout the nanocomposite formation. For this purpose, synthesized magnetite had its surface modified by acrylic acid or methacrylic acid to improve its individual encapsulation during the polymerization step, thus generating a series of magnetic nanocomposite materials containing different amounts of magnetite intended for biomedical applications. X-ray diffractometry and TEM measurements provided a mean size of approximately 8 nm for the pure magnetite nanoparticles and a spherical morphology. Acid-functionalized Fe3O4 had a size of ap proximately 6 nm, while the nanocomposites showed a size of approximately 7 nm. Magnetization measurement provided a saturation magnetization value of approximately 75 emu/g and confirmed superparamagnetic behavior at room temperature. DSC analysis showed a glass transition temperature of 65 ◦C for poly(vinyl pivalate)-based nanocomposites. The tests realized with homo polymer and magnetic composites against different cell lineages (i.e., fibroblasts, keratinocytes, and human melanoma) to evaluate the levels of cytotoxicity showed good results in the different exposure times and concentrations used, since the obtained results showed cell viability greater than 70% compared to the control group, suggesting that the synthesized materials are very promising for medical applications.

Abstract Due to the ability of microorganisms to first adhere to a material surface and then to lead to the formation of a biofilm, it is essential to develop surfaces that have antimicrobial properties. It is well known that N-halamine coatings allow us to prevent or minimize such phenomena. In the present work, various polydopamine (PDA) coatings containing chloramine functions were studied. In fact, three PDA-based films were formed by the simple immersion of a gold substrate in a dopamine solution, either at pH 8 in the presence or not of polyethyleneimine (PEI), or at pH 5 in the presence of periodate as an oxidant. These films were characterized by polarization modulation reflection absorption infrared spectroscopy and X-ray photoelectron spectroscopy analyses, and by scanning electron microscopy observations. The chlorination of these PDA films was performed by their immersion in a sodium hypochlorite aqueous solution, in order to immobilize Cl(+I) into the (co)polymers (PDA or PDA–PEI). Finally, antibacterial assays towards the Gram-negative bacteria Escherichia coli (E. coli) and the Gram-positive bacteria Staphylococcus epidermidis (S. epidermidis) were conducted to compare the bactericidal properties of these three N-halamine coatings. Regardless of the bacteria tested, the PDA coating with the best antibacterial properties is the coating obtained using periodate.