SOLVENT EXTRACTION OF 99 Tc FROM RADIOACTIVE INTERMEDIATE LIQUID WASTE BY DIBENZO-18-CROWN-6

ABSTRACT Technetium is one of the most prominent problems since its most stable specie in the environment, the pertechnetate ion, is highly mobile and considered as a long-term hazard in nuclear waste disposal. Because of the small activities of 99 Tc relative to other fission products 137 Cs or 90 Sr, and its long half-life time (t 1/2 = 2.1•10 5 yrs), 99 Tc is one of the key isotopes that should always be analyzed in the radioactive liquid waste streams from the reprocessing industry where the largest concentrations are to be expected. Furthermore, as a pure betaemitter, 99 Tc has to be isolated from the intermediate level waste (ILW) stream prior to any measurement in such complex media. We have developed a method for 99 Tc extraction providing recommendations that will be useful for extracting it from acid and basic ILW. The extraction of 99 Tc from ILW by dibenzo-18-crown-6 (DB18C6) has been investigated and a simplex optimization of key parameters involved in the procedure has allowed us to set up their best values. Experiments have been carried out on synthetic and real effluents from La Hague reprocessing plant, France, and results show that DB18C6 is highly selective towards 99 Tc. The application of this procedure has been successfully demonstrated through the analysis of actual waste streams coming from two reprocessing plants at La Hague and Marcoule, France

Influence of Light Soaking on Silicon Heterojunction Solar Cells With Various Architectures

In this article, we investigate the effect of prolonged light exposure on silicon heterojunction solar cells. We show that, although light exposure systematicallyimproves solar cell efficiency in the case of devices using intrinsic and p-type layers with optimal thickness, this treatment leads to performance degradation for devices with an insufficiently thick (p) layer on the light-incoming side. Our results indicate that this degradation is caused by a diminution of the (i/p)-layer stack hole-selectivity because of light exposure. Degradation is avoided when a sufficiently thick (p) layer is used, or when exposure of the (p) layer to UV light is avoided, as is the case of the rear-junction configuration, commonly used in the industry. Additionally, applying a forward bias current or an infrared light exposure results in an efficiency increase for all investigated solar cells, independently of the (p)-layer thickness, confirming the beneficial influence of recombination on the performance of silicon heterojunction solar cells

Analysis of nuclear proliferation resistance reprocessing and recycling technologies

The PUREX process has been progressively and continuously improved during the past three decades, and these improvements account for successful commercialization of reprocessing in a few countries. The renewed interest in nuclear energy and the international growth of nuclear electricity generation do not equate – and should not be equated -with increasing proliferation risks. Indeed, the nuclear renaissance presents a unique opportunity to enhance the culture of non-proliferation. With the recent revival of interest in nuclear technology, technical methods for prevention of nuclear proliferation are being revisited. Robust strategies to develop new advanced separation technologies are emerging worldwide for sustainability and advancement of nuclear energy with enhanced proliferation resistance. On the other hand, at this moment, there are no proliferation resistance advanced technologies. . Until now proliferation resistance as it applies to reprocessing has been focused on not separating a pure stream of weapons-usable plutonium. France, as an example, has proposed a variant of the PUREX process, the COEX TM process, which does not result on a pure plutonium product stream. A further step is to implement a process based on group extraction of actinides and fission products associated with a homogeneous recycling strategy (UNEX process in the US, GANEX process in France). Such scheme will most likely not be deployable on an industrial scale before 2030 or so because it requires intensive R&D and robust flowsheets. Finally, future generation recycling schemes will handle the used nuclear fuel in fast neutron reactors. This means that the plutonium throughput of the recycling process may increase. The need is obvious for advanced aqueous recycling technologies that are intrinsically more proliferation resistant than the commercial PUREX process. In this paper, we review the actual PUREX process along with the advanced recycling technologies that will enhance technical barriers, making plutonium diversion more difficult by not isolating plutonium or/and coexistence of fission products with plutonium

Hydrogen production from high temperature steam catalytic gasification of bio-char

Hydrogen production from the catalytic steam gasification of bio-char derived from the pyrolysis of sugar cane bagasse has been investigated in relation to gasification temperature up to 1050 °C, steam flow rate from 6 to 25 ml h−1 and type of Nickel catalyst. The catalysts used were Ni-dolomite, Ni–MgO and Ni–Al2O3, all with 10% nickel loading. The hydrogen yield in the absence of a catalyst at a gasification temperature of 950 °C was 100.97 mmol g−1 of bagasse char. However, the presence of the Ni–MgO and Ni–Al2O3 catalysts produced significantly improved hydrogen yields of 178.75 and 187.25 mmol g−1 of bagasse char respectively at 950 °C. The hydrogen yield from the char with the Ni-dolomite only showed a modest increase in hydrogen yield. The influence of gasification temperature showed that the optimum temperature to obtain the highest hydrogen yield was 950 °C. Increase in gasification temperature from 750 to 950 °C significantly increased hydrogen yield from 45.30 to 187.25 mmol g−1 of bagasse char at 950 °C, but was followed by a decrease in yield at 1050 °C. The influence of steam flow rate showed that with the increase in steam flow rate from 6 to 15 ml h−1 hydrogen yield was increased from 187.25 to 208.41 mmol g−1 of bagasse char. Further increase in steam flow rate resulted in a decrease in hydrogen yield

Back-Contacted Silicon Heterojunction Solar Cells: Optical-Loss Analysis and Mitigation

We analyze the optical losses that occur in interdigitated back-contacted amorphous/crystalline silicon heterojunction solar cells. We show that in our devices, the main loss mechanisms are similar to those of two-side contacted heterojunction solar cells. These include reflection and escape-light losses, as well as parasitic absorption in the front passivation layers and rear contact stacks. We then provide practical guidelines to mitigate such reflection and parasitic absorption losses at the front side of our solar cells, aiming at increasing the short-circuit current density in actual devices. Applying these rules, we processed a back-contacted silicon heterojunction solar cell featuring a short-circuit current density of 40.9 mA/cm(2) and a conversion efficiency of 22.0%. Finally, we show that further progress will require addressing the optical losses occurring at the rear electrodes of the back-contacted devices

Spectroscopic investigation of the formation of hypochlorite, radiolysis by-product in 5 M NaCI featuring high-energy proton beam line experiments.

Because geological salt formations are considered possible sites for radioactive waste disposal, plausible inundation scenario of salt repository will allow chloride brines to be formed, which consequently will be exposed to radiation from the waste. Key radioelements in Intermediate Level Waste (ILW),H igh Level Waste (HLW) or TRU waste have been found to be plutonium, americium, neptunium, uranium, and technetium. Therefore, the effect of radiolysis on high-saline brine under simulated repository conditions are of particular importance because it results in oxidizing chlorine-containing species, such as hypochlorite (OC1-), and hypochlorous acid (HOCI), which may oxidize actinide species to higher oxidation states. Meaningful predictions of long-term redox conditions in a nuclear repository strongly rely on estimations of G-values of the irradiation-induced formation of the oxidizers OC1- and HOCI. G-values not only depend on the total absorbed doses over the relevant timeframe, but also on the kind of irradiation involved. In fact, the G-values of hypochlorite produced by {alpha}-, {beta}-, {gamma}-, or neutron irradiation differ by an order of magnitude, depending on different LET cross-sections. To overcome the serious constrains and obstacles of conventional radiochemical work within GBq/L activity levels, we are going to simulate {alpha}-irradiation of chloride brines by the adaptation of beam-line experiments. Our long-term goal is to demonstrate how the main oxidizing chloride species such as hypochlorite caused by radiolysis may affect the overall behavior of actinides under salt repository conditions. This paper describes our first steps towards the production, the identification and the determination of these oxidizing species by beam line experiments

Spectroscopic Investigation of the Formation of Radiolysis By-Products By 13/9 MeV Linear Accelerator of Electrons (LAE) in Salt Solutions

In the near-field chemistry of a salt repository, the radiolytically-induced redox reactions in concentrated saline solution are of particular importance because the radiolysis of saline solutions results in oxidizing chlorine-containing species, which may oxidize actinide species to higher oxidation states. If the brines are irradiated, the solutions containing radiolytic species such as hypochlorite, hypochlorous acid or hydrogen peroxide, their pH and Eh may be altered. The oxidation and complexation states of actinides, which might be present in the salt brine, will change thus influencing their speciation and consequently their mobility. Furthermore, radiolytically formed oxidizing species such as ClO- or H2O2 may enhance the corrosion of the canister material. Therefore, radiation effects on salt brines must be integrated into the database, which described the chemical processes near a disposal site. Investigations in that context usually focus on the radiation chemistry of solid NaCl however our focus is on the radiolytic products, which are formed when salt brines are irradiated by a 10 MeV linear accelerator of electrons (LAE). We attempt to quantify the irradiation-induced formation of typical radiolysis by-products such as the hypochlorite ion (OCl-) by using a 13/9 MeV LAE with doses between 120 KGy to 216 KGy while monitoring the pH of the brine solutions

Back-Contacted Silicon Heterojunction Solar Cells With Efficiency >21%

We report on the fabrication of back-contacted silicon heterojunction solar cells with conversion efficiencies above 21%. Our process technology relies solely on simple and size-scalable patterning methods, with no high-temperature steps. Using in situ shadow masks, doped hydrogenated amorphous silicon layers are patterned into two interdigitated combs. Transparent conductive oxide and metal layers, forming the back electrodes, are patterned by hot melt inkjet printing. With this process, we obtain high short-circuit current densities close to 40 mA/cm2 and open-circuit voltages exceeding 720 mV, leading to a conversion efficiency of 21.5%. However, moderate fill factor values limit our current device efficiencies. Unhindered carrier transport through both heterocontact layer stacks, as well as higher passivation quality over the minority carrier-injection range relevant for solar cell operation, are identified as key factors for improved fill factor values and device performance

Transparent Electrodes in Silicon Heterojunction Solar Cells: Influence on Contact Passivation

Charge carrier collection in silicon heterojunction solar cells occurs via intrinsic/doped hydrogenated amorphous silicon layer stacks deposited on the crystalline silicon wafer surfaces. Usually, both the electron and hole collecting stacks are externally capped by an n-type transparent conductive oxide, which is primarily needed for carrier extraction. Earlier, it has been demonstrated that the mere presence of such oxides can affect the carrier recombination in the crystalline silicon absorber. Here, we present a detailed investigation of the impact of this phenomenon on both the electron and hole collecting sides, including its consequences for the operating voltages of silicon heterojunction solar cells. Based on our findings, we define guiding principles for improved passivating contact design for high-efficiency silicon solar cells

Efficient Near-Infrared-Transparent Perovskite Solar Cells Enabling Direct Comparison of 4-Terminal and Monolithic Perovskite/Silicon Tandem Cells

Combining market-proven silicon solar cell technology with an efficient wide band gap top cell into a tandem device is an attractive approach to reduce the cost of photovoltaic systems. For this, perovskite solar cells are promising high-efficiency top cell candidates, but their typical device size (<0.2 cm2), is still far from standard industrial sizes. We present a1cm2 near-infrared transparent perovskite solar cell with 14.5% steady- state efficiency, as compared to 16.4% on 0.25 cm2. By mechanically stacking these cells with silicon heterojunction cells, we experimentally demonstrate a 4-terminal tandem measurement with a steady-state efficiency of 25.2%, with a 0.25 cm2 top cell. The developed top cell processing methods enable the fabrication of a 20.5% efficient and 1.43 cm2 large monolithic perovskite/silicon heterojunction tandem solar cell, featuring a rear-side textured bottom cell to increase its near-infrared spectral response. Finally, we compare both tandem configurations to identify efficiency-limiting factors and discuss the potential for further performance improvement