The removal of Co(II) ions from aqueous media was done using three types of biochars obtained from algae waste biomass, mustard waste biomass, and soy waste biomass. The biochar samples were obtained by pyrolysis of waste biomass resulted from biofules production, at relative low temperature (600–650 °C), and this procedure can be considered a suitable alternative to reduce the volume of such waste. FTIR spectra recorded for each type of biochar reveal the presence of several functional groups that can be used as binding sites for Co(II) retention. The batch biosorption experiments were performed as a function of initial Co(II) ions concentration and contact time, at constant solution pH (5.0), sorbent dose (8.0 g/L), and room temperature (25 ± 1 °C). The sorption experiments showed that the Co(II) ions retention reaches the equilibrium in maximum 60 min, and the maximum sorption capacity follows the order: Mustard biochar (MBC—24.21 mg/g) < soy biochar (SBC—19.61 mg/g) < algae biochar (ABC—11.90 mg/g). The modeling of experimental data proves that the retention of Co(II) ions from aqueous solution occurs through electrostatic interactions, and that the sorption process takes place until a monolayer coverage is formed on the outer surface of the biochar. This information is very useful in the design of a suitable desorption system. The desorption results showed that by treating the biochar samples loaded with Co(II) ions with 0.1 mol/L HNO₃ solution, over 92% of Co(II) ions are desorbed and can be recovered, and the biochar samples can be used in at least three sorption/desorption cycles. All the experimental observations sustain the potential use of biochar obtained from different types of waste biomass as a promising alternative sorbent for the removal of Co(II) ions from aqueous media.

Hemp fibres used as a reinforcing agent and three polymeric matrices (polypropylene, bicomponent, recycled polyester) were used to obtain composite materials by needle punching and heat pressing. The influence of the hemp/matrix ratio and the nature of the matrix on the properties of the composites were analysed. The obtained composites were characterised by physical–mechanical indices, thermal analysis (thermogravimetry (TG), differential thermogravimetry (DTG) and Differential Scanning Calorimetry (DSC)), Fourier Transform Infrared Spectroscopy (FTIR-ATR) analysis, Scanning Electron Microscopy (SEM) and Chromatic measurements. The mechanical properties of composites are influenced by both the hemp/matrix ratio and the nature of the matrix. The thermal stability of composites decreased as the amount of hemp increased (for the same mass losses, the decomposition temperature decreased significantly for composites containing a quantity of hemp greater than 50%). Regarding the nature of the matrix, for the same mass loss, the highest decomposition temperature was presented by the composites containing recycled polyester as matrix, and the lowest one was presented by composites containing polypropylene fibres as matrix. The FTIR and SEM analyses highlight the changes that occurred in the structure of the composite, changes determined both by the amount of hemp in the composite and by the nature of the matrix.

Chitosan films obtained by dry phase inversion were prepared from an aqueous solution of chitosan in acetic acid. The films, of thickness less than 20 μm, were transparent, very flexible and had smooth surfaces. Increasing the film thickness induced an increase of the internal tensions and the consequent formation of a rough surface. Structural investigations by X-ray diffraction and Fourier transform IR analysis, showed that the chitosan films, as prepared, are amorphous. Further annealing to evaporate acetic acid and water traces, changed the amorphous phase into a more ordered phase, characterized by diffraction peaks at 2θ values of 9, 17, 20 and 23 degrees. Thermal investigations by TG, DTG, and DTA revealed that the decomposition of the chitosan films as prepared proceeds in two stages, starting from 180°C and 540°C.