Urea-rich sodium alginate-based hydrogel fertilizer as a water reservoir and slow-release N carrier for tomato cultivation under different water-deficit levels.

In this study, a new eco-friendly urea-rich sodium alginate-based hydrogel with a slow-release nitrogen property was prepared, and its effectiveness was evaluated in the cultivation of tomato plants under different water stress levels. The structure and performance of the hydrogel were investigated by FTIR, XRD, TGA, DTG, and SEM. The swelling and release experiments showed that prepared urea-rich hydrogel exhibited a high-water holding capacity (412 ± 4 g/g) and showed a sustained and slow nitrogen release property. A greenhouse pot experiment was conducted using two hydrogel levels (0.1 and 0.5 wt%) under two water deficit levels (30 and 70 % based on required water irrigation). Germination tests indicated that the developed hydrogel fertilizer has no phytotoxicity and has a positive impact on the germination rate even under water deficit conditions. The application of hydrogel fertilizer at 0.5 wt% significantly (p > 0.05) enhanced plant growth parameters such as leaf number, chlorophyll content, stem diameter, and plant length compared to the control treatment. The magnitude of the responses to the hydrogel fertilizer application depended on the concentration of applied hydrogel fertilizer and stress severity with the most positive effects on the growth and yield of tomato observed at a level of 0.5 %. Tomato yield was significantly enhanced by 19.58 %-12.81 %, 18.58 %-22.02 %, and 39.38 %-43.18 % for the plant amended with hydrogel at 0.1-0.5 wt% and grown under water deficit levels of 0, 30, and 70 %, respectively, compared to the control treatment.

A Novel Chitosan/Nano-Hydroxyapatite Composite for the Adsorptive Removal of Cd(II) from Aqueous Solution.

A novel polymer bio-composite based on nano-hydroxyapatite (n-Hap) and chitosan (CS) (CS/n-Hap) was synthesized to effectively address toxic cadmium ions removal from water. The composition and structure of CS/n-Hap bio-composite were analyzed through different characterization techniques. XRD patterns affirmed that the crystalline structure of n-Hap remained unaltered during CS/n-Hap synthesis, while FT-IR spectrum sustained all the characteristic peaks of both CS and n-Hap, affirming the successful synthesis of CS/n-Hap. Adsorption studies, including pH, adsorbent dosage, contact time, initial Cd(II) concentration, and temperature, were carried out to explain and understand the adsorption mechanism. Comparatively, CS/n-Hap bio-composite exhibited better Cd(II) adsorption capacity than pristine CS, with an experimental maximum uptake of 126.65 mg/g under optimized conditions. In addition, the kinetic data were well fitted to the pseudo-second-order model, indicating the formation of chemical bonds between Cd(II) and CS/n-Hap during adsorption. Furthermore, the thermodynamic study suggested that Cd(II) adsorption onto CS/n-Hap was endothermic and spontaneous. The regeneration study showed only about a 3% loss in Cd(II) uptake by CS/n-Hap after five consecutive cycles. Thus, a simple and facile approach was here developed to synthesize an eco-friendly and cost-effective material that can be successfully employed for the removal of toxic heavy metal ions from water.