Uranium chelating ability of decorporation agents in serum evaluated by X-ray absorption spectroscopy.

Internal exposure to actinides such as uranium and plutonium has been reduced using chelating agents for decorporation because of their potential to induce both radiological and chemical toxicities. This study measures uranium chemical forms in serum in the presence and absence of chelating agents based on X-ray absorption spectroscopy (XAS). The chelating agents used were 1-hydroxyethane 1,1-bisphosphonate (EHBP), inositol hexaphosphate (IP6), deferoxamine B (DFO), and diethylenetriaminepentaacetate (DTPA). Percentages of uranium-chelating agents and uranium-bioligands (bioligands: inorganic and organic ligands coordinating with uranium) dissolving in the serum were successfully evaluated based on principal component analysis of XAS spectra. The main ligands forming complexes with uranium in the serum were estimated as follows: IP6 > EHBP > bioligands > DFO ≫ DTPA when the concentration ratio of the chelating agent to uranium was 10. Measurements of uranium chemical forms and their concentrations in the serum would be useful for the appropriate treatment using chelating agents for the decorporation of uranium.

Wet chemical processing for nuclear waste glass to retrieve radionuclides.

Here, we show unexpected and significant elution behavior of various elements from simulated nuclear waste glass (NWG) in ∼10° mol dm-3 acidic solutions below 100 °C, where a borosilicate-based glass matrix has been believed to be chemically durable. Most elements like glass main components (Li, B, Na, Ca, Al, and Zn, but except for Si) and simulated radionuclides (Rb, Cs, Sr, Ba, Se, Te, Mn, Pd, Mo, rare earths, Cr, Fe, and Ni) were remarkably eluted from the simulated NWG in ∼10° M HNO3 aq with Cl- at 90 °C. Especially, the elution of Pd is governed by its coordination chemistry including a redox reaction, because Pd(0) present in the simulated NWG has to be oxidized to Pd2+ which forms [PdCl4]2- for its dissolution. While Zr in simulated NWG is sparingly eluted even in this treatment, its elution actually proceeds in 1-3 M H2SO4 aq at 90 °C thanks to strong coordination of Zr(IV) with SO42-. Through design and optimization of the leaching conditions, a protocol of the wet chemical process to retrieve the radionuclides from simulated NWG has been proposed and demonstrated.

Electrochemical Insight into the Brust-Schiffrin Synthesis of Au Nanoparticles.

The mechanism of the Brust-Schiffrin gold nanoparticle synthesis has been investigated through the use of ion transfer voltammetry at the water/1,2-dichloroethane (DCE) solution interface, combined with X-ray absorption fine structure (XAFS) of the reaction between [AuCl4](-) and thiol (RSH) in homogeneous toluene (TL) solution. Ion transfer calculations indicate the formation of [AuCl2](-) at RSH/Au ratios from 0.2-2 with a time-dependent variation observed over several days. At RSH/Au ratios above 2 and after time periods greater than 24 h, the formation of Au(I)SR is also observed. The relative concentrations of reaction products observed at the liquid/liquid interface are in excellent agreement with those observed by XAFS for the corresponding reaction in a single homogeneous phase. BH4(-) ion transfer reactions between water and DCE indicate that the reduction of [AuCl4](-) or [AuCl2](-) to Au nanoparticles by BH4(-) proceeds in the bulk organic phase. On the other hand, BH4(-) was unable to reduce the insoluble [Au(I)SR]n species to Au nanoparticles. The number and size of the nanoparticles formed was dependent on the concentration ratio of RSH/Au, as well as the experimental duration because of the competing formation of the [Au(I)SR]n precipitate. Higher concentrations of nanoparticles, with diameters of 1.0-1.5 nm, were formed at RSH/Au ratios from 1 to 2.

Metal deposition at the liquid-liquid interface.

Metal nanoparticles are readily formed, with a reasonable degree of size and shape control, using solution-based reduction methods under ambient conditions. Despite the large number of reports in this field, much of our knowledge of nanoparticle growth is largely empirical, with the relationship between particle form and growth conditions, for example, still not well understood. Many nanoparticle preparation routes actually depend on not one, but two, solution phases, i.e. the syntheses involve reaction or transfer at the liquid-liquid (organic-water) interface. This interface can be polarised electrochemically, an approach that offers promise as a route to better understanding, and ultimately control, of nanoparticle growth.

Mass-dependent and mass-independent isotope effects of zinc in a redox reaction.

We report the isotope fractionation of zinc (Zn) associated with a redox reaction between Zn(0) and Zn(II). Zn isotopes were found fractionated in pyrometallurgical biphase extraction between liquid zinc and molten chloride. The isotopic composition of Zn in the molten chloride phase was analyzed by multiple collector inductively coupled plasma mass spectrometry and reported as (m)Zn/64Zn (m = 66, 67, and 68) ratios. The observed isotope fractionation consists of the mass-dependent and mass-independent isotope effects. The contributions of the nuclear mass and the nuclear volume to the overall isotope effect were evaluated by employing first-principles quantum calculations and using reported isotope shifts in atomic spectra. The magnitude of the mass-dependent isotope effect was explained by the sum of the isotope effect via intramolecular vibrations and the correction to the Born-Oppenheimer electronic energy. The mass-independent isotope effect was correlated with the Gibbs free energy change in the redox reaction.

The development of a multichannel electrode array for retinal prostheses.

The development of a multielectrode array is the key issue for retinal prostheses. We developed a 10 x 10 platinum electrode array that consists of an 8-microm polyimide layer sandwiched between 5-microm polymonochloro-para-xylylene (parylene-C) layers. Each electrode was formed as a 30-microm-high bump by Pt/Au double-layer electroplating. We estimated the charge delivery capability (CDC) of the electrode by measuring the CDCs of two-channel electrode arrays. The dimensions of each electrode of the two-channel array were the same as those of each electrode formed on the 10 x 10 array. The results suggest that for cathodic-first (CF) pulses, 80% of electrodes surpassed our development target of 318 microC/cm2, which corresponds to the charge density of pulses of 500 micros duration and 200 microA amplitude for a 200-microm-diameter planar electrode.

Flexible and extendible neural stimulation/recording device based on cooperative multi-chip CMOS LSI architecture.

An LSI-based cooperative multi-chip neural stimulation/recording device is proposed and fabricated. The proposed multi-chip device consists of small (600 microm x 600 microm in the present design) intelligent neural stimulation/recording chips (unit chip). The unit chip has a neural stimulation/recording electrode array and individual control circuit. It can work with other unit chips cooperatively. One can configure any number of the unit chips as the multi-chip neural stimulation/recording device. Compared to conventional single-chip architecture, the proposed multi-chip architecture has advantages in thinness, mechanical strength and flexibility, and extendibility. That makes the multi-chip neural stimulation/ recording device more suitable for in vivo applications than conventional single-chip devices. Packaging technology for cooperative multi-chip device is also discussed. We developed a thin, flexible packaging technique for the multi-chip neural stimulation/recording device and LSI-compatible Pt/Au stacked biocompatible bump electrode.