No abstract

All-oxide thermoelectric modules for energy harvesting are attractive because of high-temperature stability, low cost, and the potential to use nonscarce and nontoxic elements. Thermoelectric modules are mostly fabricated in the conventional π-design, associated with the challenge of unstable metallic interconnects at high temperature. Here, we report on a novel approach for fabrication of a thermoelectric module with an in situ formed p–p–n junction made of state-of-the-art oxides Ca 3 Co 4– x O 9+δ (p-type) and CaMnO 3 –CaMn 2 O 4 composite (n-type). The module was fabricated by spark plasma co-sintering of p- and n-type powders partly separated by insulating LaAlO 3 . Where the n- and p-type materials originally were in contact, a layer of p-type Ca 3 CoMnO 6 was formed in situ. The hence formed p–p–n junction exhibited Ohmic behavior and a transverse thermoelectric effect, boosting the open-circuit voltage of the module. The performance of the module was characterized at 700–900 °C, with the highest power output of 5.7 mW (around 23 mW/cm 2 ) at 900 °C and a temperature difference of 160 K. The thermoelectric properties of the p- and n-type materials were measured in the temperature range 100–900 °C, where the highest zT of 0.39 and 0.05 were obtained at 700 and 800 °C, respectively, for Ca 3 Co 4– x O 9+δ and the CaMnO 3 –CaMn 2 O 4 composite.

Lanthanum doped strontium titanate is a potential n-type thermoelectric material at moderate and high temperatures. (La0.12Sr0.88)0.95TiO3 ceramics were prepared by two different routes, conventional sintering at 1500 °C and spark plasma sintering at temperatures between 925 and 1200 °C. Samples with grain size between 40 nm and 1.4 µm were prepared and characterized with respect to their thermoelectric transport properties at temperatures between 100 and 900 o C under reducing conditions (H2/H2O-buffer mixtures). The thermal conductivity was significantly reduced with decreasing grain size reaching a value of 1.3 W . m -1. K -1 at 600 °C for grain size of 40 nm and porosity of 19 %. Electrical conductivity increased with increasing grain size showing a maximum of 500 S . cm -1 at 200 °C for a grain size of 1.4 µm. The highest figure-of-merit (zT) was measured for samples with 1.4 m average grain size reaching 0.2 at 500 °C.

In this contribution, a composite from bentonite (B), CoFe2O4 (CF), and hydroxyapatite (HAP) was developed by chemical synthesis route for adsorption of a lead ion, Pb (II) from wastewater. Initially, a composite of B/CF was synthesized by varying the weight ratio of CF, i.e., (1–x)B/(x)CF (x = 0.05, 0.15, 0.25, 0.50), followed by ternary composite synthesis, which was formulated from the sample of (0.85B/0.15CF) and different weight ratios of HAP, i.e., (1–y)[(0.85B/0.15CF)]/yHAP where y = 0.25, 0.35 and 0.45 weight ratios of HAP. The sample of 0.85B/0.15CF was found to be optimal in its adsorption capacity of about 20 mg g−1 from the binary composite samples, while among the ternary composites, a sample with a composition of 0.65[(0.85B/0.15CF)]/0.35HAP revealed an optimum adsorption capacity of about 36 mg g−1, which was then selected for further studies. The adsorption kinetics of Pb (II) by the optimum 0.65[(0.85B/0.15CF)]/0.35HAP sample was studied at different contact times from 30–120 min, where the equilibrium was reached at around 90 min of contact time and the kinetic behavior adopted Pseudo-second order adsorption mechanism. The initial concentration of Pb (II) was also varied from 50–200 mg l−1 to study the adsorption isotherm, which resulted that adsorption capacity of 0.65[(0.85B/0.15CF)]/0.35HAP towards Pb (II) was increased to about 66 mg g−1 and the adsorption isotherm data best fitted with Langmuir adsorption isotherm model. Therefore, the result of this study pinpoints that the present composite material is a potential candidate for the adsorption of Pb (II) ion.

Nowadays, water pollution is a major concern to the globe. For this reason, various research works has been done to access pure water thereby minimizing the effect of pollutants. In this work, the cobalt doped ZnO (Co-doped ZnO) via the accumulation of cobalt ion onto Eichhornia crassipes plant tissue for different days and combined with zinc precursor was synthesized. The resulting catalyst powder samples were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), X-Ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM), and Ultraviolet–vis (UV–vis) spectroscopy, and microwave plasma atomic emission spectrometer (MP-AES). The catalysts were also tested for the photocatalytic degradation of methylene blue (MB) in the presence of H2O2 under visible light irradiation. The best catalytic activity was gained by the 8th-days accumulation of cobalt ion onto the Eichhornia crassipes plant tissue and 99.6% of the dye was degraded within 45 min. However, 69.6, 65.7, 73.6, and 94.8% of MB dye was degraded by 1, 2, 4, and 6 days accumulations. Hence, removal of toxic heavy metal by using Eichhornia crassipes plant and recycling in the wastewater treatment gain is highly appreciated. Moreover, the Co-doped ZnO photocatalysts could enhance the photocatalytic activities due to suppressing of the electron and hole recombination and the porosity of the catalysts resulted from the Eichhornia crassipes plant after calcination.