RESUMO
Driven by the environmental stress caused by plastics, the interest on eco-friendly polymers has attracted the attention of researchers and industry. Thermoplastic starch (TPS) and poly (ε-caprolactone) (PCL) blends are good examples of sustainable material, exhibiting synergism between economic viability and properties. However, its biodegradability aligned to nutrients release has been less explored in agricultural applications. Herein, it is proposed the investigation of biodegradability of urea plasticized TPS and PCL blends, compatibilized with PCL grafted with maleic anhydride (PCL-g-MA), aiming fertilizers and sustainable agricultural products. The blends were prepared in a twin-screw extruder using a flat film die. The mechanical, thermal, morphological, and physical properties of TPS-PCL films were characterized, including biodegradation analysis via Bartha respirometer and nitrogen release in the soil. The films presented biodegradability and nitrogen release as a function of TPS content on blends formulation, presenting flexibility and robust mechanical properties. These findings may open a way of multifunctional agricultural products applied as fertilizer materials through economical and sustainable mulching films.
RESUMO
The coating of fertilizers with polymers is an acknowledged strategy for controlling the release of nutrients and their availability in soil. However, its effectiveness in the case of soluble phosphate fertilizers is still uncertain, and information is lacking concerning the chemical properties and structures of such coatings. Here, an oil-based hydrophobic polymer system (polyurethane) is proposed for the control of the release of phosphorus from diammonium phosphate (DAP) granules. This material was systematically characterized, with evaluation of the delivery mechanism and the availability of phosphate in an acid soil. The results indicated that thicker coatings can change the maximum nutrient availability toward longer periods, such as 4.5-7.5 wt % DAP coated, that presented the highest concentrations at 336 h, as compared to 168 h for uncoated DAP. In contrast, DAP treated with 9.0 wt % began to increase the concentration after 168 h until it results in maximum release at 672 h. These effects could be attributed to the homogeneity of the polymer and the porosity. The strategy successfully provided long-term availability of a phosphate source.