In this study, we present a long-term water management model which can be an important tool for the ordinary management of a reservoir. The model can be made simple and applicable in a graphic form. The key point of the model is that the sedimentation rate of solids can be modeled according to a power law. The basic equation of the model is tested using bathymetric surveys of different dams located in different parts of the world. Robustness and predictive power are evaluated both numerically and by comparison with satellite results. Then the model is transformed into the form of a management plot and applied to the real case of the Camastra dam.

In this work, a peroxydisulfate (PDS)-based advanced oxidation process was used for removing diuron from water. The effect of heat and MnO2 as PDS activators was explored. It was found that diuron degradation obeyed zero-order kinetics in the presence of heat-activated PDS. The relative contribution of MnO2 to the diuron degradation decreased with the increasing temperature. At the highest temperature investigated, T = 55 °C, complete diuron removal was achieved in less than 75 min. A kinetic model for describing the rate of diuron degradation was proposed and successfully applied to the experimental data.

A simple model is proposed to calculate the dimerization constant of a dye in non-aqueous solvents. Alkan-1ols of the formula H–(CH2)n–OH are used to study the spectroscopic behavior of Nile Red dye. The number n varied from 1 to 8 to modulate the medium hydrophobicity. Generally, Nile red is used to localize lipid droplets within cells. This molecule is non-fluorescent in water and other polar solvents but undergoes fluorescence enhancement and large absorption and emission blue shifts in non-polar environments. The calculated equilibrium constants suggest that the aggregation process is solvent-assisted. The absorption and fluorescence emission spectra reveal a marked red shift, which is studied by breaking the wavelength of the maximum band into two terms, showing the contribution of the solvent and the effect of the dye concentration. Both contributions were investigated as a function of the number n, and it was found that alkan-1ols with large n tend to aggregate and produce a smaller red shift. Conversely, it was also noticed that short-chain alkan-1ols stabilize the excited state of the dye via H-bond and the red shift increases. The hydrophilicity of the medium was found to be modulated by adding pure water, in a controlled way, to the binary systems dye–H–(CH2)n–OH (n = 1–8). The quantification of solvent hydrophilicity is described with the ratio R = water moles/alcohol moles. From this investigation, we realized that the absorption spectra values are strictly connected with the R parameter. In this context, we realized that fluorescence emission spectra allow us to determine the adjustable parameters.

In the present paper, a simple method for analyzing the self-aggregation of dyes in a solution by a UV-visible absorption measurements is proposed. The concept of excess absorbance is introduced to determine an equation whose coefficients determine the parameters of the aggregation equilibrium. The computational peculiarities of the model are first discussed theoretically and then applied to sodium fluorescein in polar protic and aprotic solvents, as well as in aqueous solutions of methylene blue, which is a cationic dye. Although the experimental responses are very different, the model appears to work equally well in both cases. The model reveals that the trimer is the most likely configuration in both solvents. Furthermore, aggregation is strongly favored for the protic solvent. Interestingly, the model establishes that in aqueous solutions of methylene blue, the tetramer is the predominant form, which has long been assumed and recently demonstrated with sophisticated computational techniques.

In tissue regeneration, biomaterials facilitate biological processes. However, a treatment with biomaterials will be successful only if supported by simple and inexpensive technologies which stimulate the regenerative processes. The present study focused on the possibility of creating formulations from which then to obtain suitable materials for the regeneration of heart tissue. The experimental procedure for precipitation of polymer- nanoparticles was modified ad hoc to obtain hybrid poly lactic-co-glycolic acid (PLGA)-phospholipid nanoparticles. The properties of the formulations produced by direct PLGA-phospholipid co-precipitation depend on the mass ratio R= polymer mass/phospholipid mass. The value of this parameter allows us to modulate the properties of the formulations. Formulations with R = 1.5, 2.3, 4, and 9 were prepared, and for each of them the particle-size distribution obtained by dynamic light scattering was studied. All samples showed that the hydrodynamic diameter decreases with increasing R value. This behavior is interpreted as polymer coil shrinkage due to contacts with the non-solvent. The spreadability and ease of obtaining thin sheets were evaluated for each formulation. The formulation with R=4 resulted in a homogeneous and easily workable material in thin sheets.