Structural Control Enables Catalytic and Electrocatalytic Activity of Porous Tetrametallic Nanorods.

Integrating more than one type of metal into a nanoparticle that has a well-defined morphology and composition expands the functionalities of nanocatalysts. For a metal core/porous multimetallic shell nanoparticle, the availability of catalytically active surface sites and molecular mass transport can be enhanced, and the multielemental synergy can facilitate intraparticle charge transport. In this work, a reliable and robust synthesis of such a functional tetrametallic nanoparticle type is presented, where a micro- and mesoporous PdPtIr shell is grown on Au nanorods. The effect of critical synthesis parameters, namely temperature and the addition of HCl are investigated on the hydrodynamic size of the micellar pore template as well as on the stability of the metal chloride complexes and various elemental analysis techniques prove composition of the porous multimetallic shell. Due to the synergistic properties, the tetrametallic nanorods possess extensive negative surface charge making them a promising catalyst in reduction reactions. Dye degradation as well as the conversion of p-nitrophenol to p-aminophenol is catalyzed by the supportless nanorods without light illumination. By depositing the particles onto conductive substrates, the nanostructured electrodes show promising electrocatalytic activity in ethanol oxidation reaction. The nanocatalyst presents excellent morphological stability during all the catalytic test reactions.

Interactions between C-steel and blended cement in concrete under radwaste repository conditions at 80 °C.

Deep geological repository is widely considered as the preferred solution for the final disposal of high-level radioactive waste. Investigation representative of the Hungarian disposal concept was conducted using mock-up diffusion cells to study the chemical changes of S235JR carbon steel canister and CEM II/B concrete of the Public Limited Company for Radioactive Waste Management under anerobic and water saturated conditions at 80 °C. Micro-Raman, Scanning Electron Microscopy-Energy Dispersive X-ray Spectroscopy, fluid and potentiometric analysis were performed over a period of 12 months. The analysis was supported by thermodynamic and reactive transport modeling using the HYTEC code. The findings revealed that a uniform corrosion process occurred, leading to rapid passivation of the C-steel with magnetite as the primary corrosion product. Modeling demonstrated that the increase in temperature to 80 °C and the chemical evolution of the concrete did not significantly affect the corrosion passivation process. Although the formation of Fe-siliceous hydrogarnets is thermodynamically possible at 80 °C, it did not jeopardize magnetite passivation. The results show that the passivation of the containers occurred under the test conditions and this is a promising result for further investigations.

Characterization of Simulated Liquid Radioactive Waste in a New Type of Cement Mixture.

There is still a safety challenge for the long-term stabilization of nuclear waste. Due to its affordable price and easy manufacturing, cement is one of the most promising materials to immobilize a large volume of low- and intermediate-level radioactive liquid waste. To investigate the effect of borate on the cementation of radioactive evaporator concentrates and to provide more data for solidification formula optimization, simulated liquid waste in various concentrations was prepared. Different borate concentrations were solidified in ordinary Portland cement (OPC) and in two new cement compositions with water resistance and boron-binding additives. The chemical and mechanical properties were investigated for nine cementitious samples, together with three compositions in three concentrations. The leaching rate of the boron is lower in the case of a high strength cement mixture. The compressive strengths of the solidified waste correlate with the leaching rates of the boron. The leaching rates of Ca were changed with the cement composition and even with the boron concentrations; first, they were lower in the initial OPC in the case of the same boron concentration (50 g/L); second, they were lower at a higher boron concentration (250 g/L) for the OXY-B composition. The simulated liquid waste with higher boron concentrations solidified with newly developed cement composition (OXY-B) shows a homogeneous boron distribution in the volume of the cement cylinder both before and after leaching. The formulas of OXY and OXY-B developed in this application were effective for cementation of the simulated borate evaporator concentrates.