Eucalyptus Leaves as Potential Indicators of Gold Mine in Indonesia

Eucalyptus is a plant that is able to absorb gold (Au) particles from the soil and store them in the leaves. Eucalyptus roots have the ability to penetrate the soil of the calcrete zone, which is rich in the mineral calcium (Ca). Calcium is a chemical element with the symbol Ca and atomic number 20. As an alkaline earth metal, calcium is a reactive metal that forms a dark oxide-nitride layer when exposed to air. and contains Au particles as impurities, making this plant a potential natural indicator (biogeochemical) of potential Au metal mining. The Au content in eucalyptus leaves can be determined by using the XRF (X-Ray Fluorescence) instrumentation material analysis method for qualitative analysis and AAS (Atomic Absorption Spectroscopy) for quantitative results. The form of XRF characterization of the intensity versus energy spectrum of certain elements from the XRF analysis results obtained is a spectrum with a peak power of 9.731 keV which indicates the presence of Au metal in the sample. The results obtained qualitatively are the Au metal content in the eucalyptus leaf sample of (9.0 ± 0.5) ppm. However, the Au metal content in each leaf sample was different. This provides information that Eucalyptus from different plants has the potential to be a biogeochemical indicator of potential Au metal mining in Indonesia

Intermetallic PdZn nanoparticles catalyze the continuous-flow hydrogenation of alkynols to cis-enols

Designing highly active and stable lead-free palladium-based catalysts without introducing surfactants and stabilizers is vital for large-scale and high-efficiency manufacturing of cis-enols via continuous-flow semi-hydrogenation of alkynols. Herein, we report an intermetallic PdZn/ZnO catalyst, designed by using the coupling strategy of strong electrostatic adsorption and reactive metal-support interaction, which can be used as a credible alternative to the commercial PdAg/Al2O3 and Lindlar catalysts. Intermetallic PdZn nanoparticles with electron-poor active sites on a Pd/ZnO catalyst significantly boost the thermodynamic selectivity with respect to the mechanistic selectivity and therefore enhance the selectivity towards cis-enols. Based on in situ diffuse reflectance infrared Fourier-transform spectra as well as simulations, we identify that the preferential adsorption of alkynol over enol on PdZn nanoparticles suppresses the over-hydrogenation of enols. These results suggest the application of fine surface engineering technology in oxide-supported metal (particles) could tune the ensemble and ligand effects of metallic active sites and achieve directional hydrogenation in fine chemical synthesis.

Effect on Current Density on Zero Charge Corrosion Protection of Pure Mg in 3.5% NaCl Solution

The cathodic protection uses two-electrode polarization, which requires large currents and substantial voltages. Efforts are being made to identify possibilities for improvements by developing zero-charge corrosion protection techniques. Studies were performed to determine the zero-charges potential effect by analyzing corrosion signs on reactive metal samples such as pure Mg. Mg samples were fed by current/ voltage pulses for 120 hours, with specified pulse parameters and varied Ecorr- offsets, ranging from +2 to -218 mV. The volumetric hydrogen gas collection technique is used to determine the hydrogen evolution rate. Surface observation is carried out by stereomicroscope to determine the presence of corrosion signs on the sample surface. Overall, all current densities and hydrogen evolution rates had very low readings on the studied Ecor offset parameters. Mg samples fed with pulses at -1800 and -1900 mV vs SCE revealed zero charge potential effects since their surface was clean and showed no indications of corrosion even after being exposed to the corrosive solution for 120 hours. Thus, corrosion protection is successfully done and meets the Epzc condition.

Development of Synthesis and Fabrication Process for Mn-CeO2 Foam via Two-Step Water-Splitting Cycle Hydrogen Production

The effects of doping manganese ions into a cerium oxide lattice for a thermochemical two-step water-splitting cycle to produce oxygen and hydrogen and new synthesis methods were experimentally investigated. In order to comparison of oxygen/hydrogen producing performance, pristine CeO2, a coprecipitation method for Mn-CeO2, and a direct depositing method for Mn-CeO2 with different particle sizes (50~75, 100–212, over 212 μm) and doping extents (0, 5, 15 mol%) were tested in the context of synthesis and fabrication processes of reactive metal oxide coated ceramic foam devices. Sample powders were coated onto zirconia (magnesium partially stabilized zirconia oxide, MPSZ) porous foam at 30 weight percent using spin coating or a direct depositing method, tested using a solar reactor at 1400 °C as a thermal reduction step and at 1200 °C as a water decomposition step for five repeated cycles. The sample foam devices were irradiated using a 3-kWth sun-simulator, and all reactive foam devices recorded successful oxygen/hydrogen production using the two-step water-splitting cycles. Among the seven sample devices, the 5 mol% Mn-CeO2 foam device, that synthesized using the coprecipitation method, showed the greatest hydrogen production. The newly suggested direct depositing method, with its contemporaneous synthesis and coating of the Mn-CeO2 foam device, showed successful oxygen/hydrogen production with a reduction in the manufacturing time and reactants, which was lossless compared to conventional spin coating processes. However, proposed direct depositing method still needs further investigation to improve its stability and long-term device durability.

Perineuronal Nets and Metal Cation Concentrations in the Microenvironments of Fast-Spiking, Parvalbumin-Expressing GABAergic Interneurons: Relevance to Neurodevelopment and Neurodevelopmental Disorders

Because of their abilities to catalyze generation of toxic free radical species, free concentrations of the redox reactive metals iron and copper are highly regulated. Importantly, desired neurobiological effects of these redox reactive metal cations occur within very narrow ranges of their local concentrations. For example, synaptic release of free copper acts locally to modulate NMDA receptor-mediated neurotransmission. Moreover, within the developing brain, iron is critical to hippocampal maturation and the differentiation of parvalbumin-expressing neurons, whose soma and dendrites are surrounded by perineuronal nets (PNNs). The PNNs are a specialized component of brain extracellular matrix, whose polyanionic character supports the fast-spiking electrophysiological properties of these parvalbumin-expressing GABAergic interneurons. In addition to binding cations and creation of the Donnan equilibrium that support the fast-spiking properties of this subset of interneurons, the complex architecture of PNNs also binds metal cations, which may serve a protective function against oxidative damage, especially of these fast-spiking neurons. Data suggest that pathological disturbance of the population of fast-spiking, parvalbumin-expressing GABAergic inhibitory interneurons occur in at least some clinical presentations, which leads to disruption of the synchronous oscillatory output of assemblies of pyramidal neurons. Increased expression of the GluN2A NMDA receptor subunit on parvalbumin-expressing interneurons is linked to functional maturation of both these neurons and the perineuronal nets that surround them. Disruption of GluN2A expression shows increased susceptibility to oxidative stress, reflected in redox dysregulation and delayed maturation of PNNs. This may be especially relevant to neurodevelopmental disorders, including autism spectrum disorder. Conceivably, binding of metal redox reactive cations by the perineuronal net helps to maintain safe local concentrations, and also serves as a reservoir buffering against second-to-second fluctuations in their concentrations outside of a narrow physiological range.