Investigation of elemental composition in red teff grains using inductively coupled plasma optical emission spectroscopy (ICP OES), Sire District, Arsi zone, Ethiopia.

BACKGROUND: Minerals are important not only for better plant growth and development but also for human and animal nutrition. It is known that east and west Gojam in the Amhara region and east and west Shoa areas in the Oromia region Ethiopia's most teff growing areas. However, there is no information on the mineral content and nutritional worth of Teff Sire district, Arsi zone, Ethiopia. Since ICP OES is a powerful technique to examine elemental compositions even in lower concentration, it is used in this work to investigate the elemental composition of red teff samples. METHODS: The elemental compositions of red Teff grain samples were determined using ICP-OES from three sites: S1, S2, and S3 of Sire district, Arsi zone, Ethiopia. Wet digestion of the teff samples was carried out by weighing 0.5 g red teff sample and digested with 8 ml HNO3 and 2 ml H2O2 (30%) for 3:00 h at a temperature of 100℃ on hot plate. The investigations of method validation, limit of detection and limit of quantification were also carried out. RESULTS: The average amount of elements in red teff sample obtained as 172-280 mg/kg Fe, 13-76 mg/kg Mn, 8.2-8.5 mg/kg Cu, 24-26 mg/kg Zn, and toxic trace elements 0.12-0.29 mg/kg Pb and 0.15-0.22 mg/kg Cd. The limit of detection found in ranges from 0.21 mg Kg-1 to 10.44 mg Kg-1 whereas quantification limit resulted in 0.7 mg Kg-1 to 34.8 mg Kg-1 for the metals under consideration. The method was validated by its linear range in the concentration range of 0.028-1.4 ppm or 0.056-2.8 ppm and excellent recovery result was achieved in the range of 90-120%. CONCLUSION: This study aimed to investigate the mineral content in red teff cultivated in Ethiopia specifically Arsi zone by using ICP OES. From the obtained results, Iron was the first abundant essential element in red teff compared to Mn, Cu and Zn. The level of trace elements: Cd and Pb in the samples slightly above the acceptable limit, possibly due to agricultural practices like usage of fertilizers, pesticides, and other industrial products. Overall, this red teff elemental composition information contributes to the nutrition database and food safety in Ethiopia and beyond.

Enhanced photocatalytic degradation of methylene blue dye using eco-friendly synthesized rGO@ZnO nanocomposites.

Industrial chemical pollutants such as methylene blue (MB) dye are released into the water body and potentially cause harm to the human and aquatic biosphere. Therefore, this study aims to synthesize eco-friendly nanocatalysts, i.e., reduced graphene oxide (rGO), zinc oxide (ZnO), and reduced graphene oxide-zinc oxide (rGO@ZnO) nanocomposites, for efficient photocatalytic degradation of MB dye. A graphite rod was obtained from waste dry cell batteries for the electrochemical exfoliation synthesis of graphene oxide (GO) and rGO. For the eco-friendly synthesis of ZnO and rGO@ZnO nanocatalysts, Croton macrostachyus leaf extract was used as a reducing and capping agent. The synthesized nanocatalysts were characterized using a UV-Vis spectrophotometer, Fourier transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy with energy-dispersive X-ray. The eco-friendly synthesized rGO, ZnO, and rGO@ZnO nanocatalysts were applied for the photocatalytic degradation of MB dye using direct sunlight irradiation. At optimum parameters, photocatalytic degradation of MB dye efficiency reached up to 66%, 96.5%, and 99.0%, respectively. Furthermore, kinetics of the photodegradation reaction based on rGO, ZnO, and rGO@ZnO nanocatalysts follow pseudo-first-order with a rate constant of 2.16 × 10-3 min-1, 4.97 × 10-3 min-1, and 5.03 × 10-3 min-1, respectively. Lastly, this study promotes a low catalyst load (20 mg) for the efficient photodegradation of MB dye.

Structural Engineering of Organic D-A-π-A Dyes Incorporated with a Dibutyl-Fluorene Moiety for High-Performance Dye-Sensitized Solar Cells.

Structural engineering of the light-harvesting dyes employed in DSSCs (dye-sensitized solar cells) with a systematic choice of the electron-donating and -accepting groups as well as the π-bridge allows the (photo)physical properties of dyes to match the criteria needed for improving the DSSC efficiency. Herein, we report an effective approach of molecular engineering of DSSC sensitizers, aiming to gain insights on the configurational impact of the fluorenyl unit on the optoelectronic properties and photovoltaic performance of DSSCs. Five new organic dyes (GZ116, GZ126, GZ129, MA1116, and MA1118) with a D-A-π-A framework integrated with a fluorenyl moiety were designed and synthesized for DSSCs. The fluorenyl unit is configured as part of the π-spacer for the GZ series, whereas it connected on the electron-deficient quinoxaline motif for the MA series. The devices fabricated from the MA1116 sensitizer produced the best performance under standard AM 1.5 G solar conditions as well as dim-light (300-6000 lx) illumination. The devices fabricated from MA1116 displayed a PCE of 8.68% (Jsc = 15.00 mA cm-2, Voc = 0.82 V, and FF = 0.71) under 1 sun and 26.81% (Jsc = 0.93 mA cm-2, Voc = 0.68 V, and FF = 0.76) under 6000 lx illumination. The device efficiency based on dye MA1116 under 1 sun outperformed that based on the standard N719 dye, whereas a comparable performance between devices based on MA1116 and N719 was achieved under dim-light conditions. A combination of enhancing the charge separation, suppressing dye aggregation, and providing better insulation that prevents the oxidized redox mediator from approaching the TiO2 surface all contribute to the superior performance of DSSCs fabricated based on these light-harvesting dyes. The judicious integration of the fluorenyl unit in a D-A-π-A-based DSSC would be a promising strategy to boost the device performance.