Structural characterization of GaN epilayers on silicon: Effect of buffer layers

Cross-sections of GaN/AlN/3C-SiC/Si(111) system have been studied by electron microscopy techniques. A nanometer thick buffer layer of silicon carbide on Si(111) substrate was formed using an original solid-phase epitaxy method. The subsequent layers of gallium nitride and aluminum nitride were grown by the method hydride-chloride vapor phase epitaxy. The resulting GaN layers display neither threading dislocations nor cracks on any scale. The main fraction of defects in GaN layers have the form of dislocation pileups that are localized at and oriented parallel to the GaN/AlN interface. The dislocation density in the obtained GaN layers is (1–2) × 10⁹ cm⁻², which corresponds to a minimum level reported in the available literature. The buffer AlN layer contains nanopores, which reduce the level of stresses at the GaN/AlN interface and thus almost completely inhibit the formation of threading dislocations.     

Effect of corrosion products on the Pu partitioning in rocks of reservoir horizon upon interaction with acidic solutions under hydrothermal conditions

Plutonium sorption on various types of sands of reservoir horizon depends on the presence of corrosion products in solutions simulating highly saline acidic (pH 2.4) liquid radioactive waste (LRW) under hydrothermal conditions (T = 150°C, 50 h). The effect of corrosion products (Fe, Cr) present in LRW consists not only in considerably increased Pu sorption, but also in increased fraction of its strongly fixed fraction. α-Track radiography revealed essentially heterogeneous distribution of Pu between mineral phases of sands of reservoir horizon after interaction with simulated LRW and predominant association of Pu with separate phases containing Fe and Cr (data of X-ray microanalysis based on scanning electron microscopy, SEM-EDX). Examination by Raman spectroscopy and X-ray diffraction analysis showed that the phases responsible for the predominant sorption of Pu are phases of Cr-containing hematite.     

Redox and complexation interactions of neptunium(V) with quinonoid-enriched humic derivatives

Actinides in their higher valence states (e.g., MO2+ and MO2(2+), where M can be Np, Pu, etc) possess a higher potential for migration and in turn pose a substantial environmental threat. To minimize this potential for migration, reducing them to lower oxidation states (e.g., their tetravalent state) can be an attractive and efficient remedial process. These lower oxidation states are often much less soluble in natural aqueous media and are, therefore, less mobile in the environment. The research presented here focuses on assessing the performance of quinonoid-enriched humic derivatives with regardsto complexing and/ or reducing Np(V) present in solution. These "designer" humics are essentially derived reducing agents that can serve as reactive components of a novel humic-based remediation technology. The derivatives are obtained by incorporating different quinonoid-moieties into leonardite humic acids. Five quinonoid-derivatives are tested in this work and all five prove more effective as reducing agents for selected actinides than the parent leonardite humic acid, and the hydroquinone derivatives are better than the catechol derivatives. The reduction kinetics and the Np(V) species formed with the different derivatives are studied via a batch mode using near-infrared (NIR)-spectroscopy. Np(V) reduction by the humic derivatives under anoxic conditions at 293 K and at pH 4.7 obeys first-order kinetics. Rate constants range from 1.70 x 10(-6) (parent humic acid) to 1.06 x 10(-5) sec(-1) (derivative with maximum hydroquinone content). Stability constants for Np(V)-humic complexes calculated from spectroscopic data produce corresponding Logbeta values of 2.3 for parent humic acid and values ranging from 2.5 to 3.2 at pH 4.7 and from 3.3 to 3.7 at pH 7.4 for humic derivatives. Maximum constants are observed for hydroquinone-enriched derivatives. It is concluded that among the humic derivatives tested, the hydroquinone-enriched ones are the most useful for addressing remedial needs of actinide-contaminated aquifers.