The electrochemical separation of uranium from cerium in LiCl–KCl eutectic and the electrochemical behavior of Ce(III) were studied. According to the cyclic voltammogram of Ce(III) and the former result of U(III), electrodeposition potential was determined at ?1.65 V (vs Ag/AgCl). The uranium metal was successfully deposited and separated from cerium. The morphology of deposit and cross section of electrode were investigated by SEM, firstly uranium deposit alloys with stainless steel and forms a thin transition layer, and secondly the uranium metal layer grows from the transition layer. The separation factors of uranium/cerium on different recovery ratios were determined through a series of steps. It was found that the content of cerium in the deposit and separation factors declined with increasing the initial concentration of U3+ in molten salts; the separation factors remained stable at around 20 in different uranium recovery ratios. 相似文献
Two‐dimensional (2D) copper‐based ternary and quaternary semiconductors are promising building blocks for the construction of efficient solution‐processed photovoltaic devices at low cost. However, the facile synthesis of such 2D nanoplates with well‐defined shape and uniform size remains a challenge. Reported herein is a universal template‐mediated method for preparing copper‐based ternary and quaternary chalcogenide nanoplates, that is, CuInS2, CuInxGa1−xS2, and Cu2ZnSnS4, by using a pre‐synthesized CuS nanoplate as the starting template. The various synthesized nanoplates are monophasic with uniform thickness and lateral size. As a proof of concept, the Cu2ZnSnS4 nanoplates were immobilized on a Mo/glass substrate and used as semiconductor photoelectrode, thus showing stable photoelectrochemical response. The method is general and provides future opportunities for fabrication of cost‐effective photovoltaic devices based on 2D semiconductors. 相似文献
The mass of the tritium produced in 6Li(n,α)T reaction was obtained by quantitatively analyzing the byproduct 4He with mass spectrometer. The self-expending seal method was employed to quantitatively prepare the Li–Pb alloy targets in room temperature. They were irradiated for 2 h in two rabbit irradiation channels in Xi’an pulsed reactor and measured after cooling 15 days. A sample purifying unit was set up to get rid of the hydrogen isotopes to remarkably reduce the interference to helium isotopes when measuring. And the sample disposal platform including purifying unit was testified with simulative gas and nature atmosphere. The targets were melted at 700 °C to release most of the 4He atoms which were measured by adding dilution gas 3He. And it was testified that 4He had released completely by repetitiously melting the targets. This approach had solved the problem that the tritium couldn’t be accurately determined by directly analyzing it because of non-complete releasing from lithium alloy. 相似文献
Components of co-continuous phase can form an interpenetrating network structure, which has great potential to synergistically improve the mechanical properties of the blends, and to impart the functional blends superior electrical conductivity and permeability. In this work, the effects of shear rates (50–5000 s?1) at different temperatures on the phase morphology, phase size and lamellar crystallites of biodegradable co-continuous polybutylene terephthalate (PBAT)/polybutylene succinate (PBS) blend are quantitatively investigated. The results show that the above features of the PBAT/PBS have a strong dependence on the shear flow and thermal field. The co-continuous phase of the blend is well maintained at 130 °C. Interestingly, this phase structure transforms into a “sea-island” structure at 160 °C, which gradually recovers to a co-continuous phase when the shear rate increases from 1000 s?1 to 5000 s?1. The phase size decreases with the increase of shear rate both at 130 °C and 160 °C due to the refinement and deformation of phase structures caused by strong shear stress. Unexpectedly, a unique phenomenon is observed that the shear-induced lamellar crystallites are oriented perpendicular to shear direction in the range of 500–5000 s?1 at 130 °C, while the orientation of lamellar crystallites at 160 °C is along the shear direction within the whole range of shear rates. The degree of orientation for the PBAT/PBS blend crystals increases first and then decreases at both temperatures above. In addition, the range of shear rate has reached the level in the industrial processing. Therefore, this work has important guiding significance for the regulation of the co-continuous phase structure and the performance for the blend in the practical processing.
Combining photothermal therapy and radiotherapy(PTT-RT) with reducing tumor hypoxia acts as an important antitumor modality. However, it is a great challenge to realize photothermal therapy, radiotherapy and exogenous oxygen supply in one nanosystem. To realize a combination of the three functions, we fabricated a red blood cell membrane(RBCm)-camouflaged, red blood cell content(RBCc) and the copper sulfide(CuS) co-loaded dendritic large pore mesoporous silica nanoparticle(DLMSN/CuS/RBCc/ RBCm). The cell membrane coating endowed the nanoparticles with good stability in the physiological environment, and CuS allowed the nanoparticle exhibiting good photothermal and radiosensitization properties. RBCc loaded nanoparticle DLMSN/CuS/RBCc enhanced superior anti-tumor effect than DLMSN/CuS during combined PTT-RT therapy because the introduction of RBCc increased the exogenous oxygen supply. The in vitro study further demonstrated that the combination of photothermal therapy and radiotherapy induced superior antitumor efficacy than single therapy. Our work thus presents a unique multifunctional nanoscale platform favorable for combined PTT and RT. 相似文献
Thermal- and light-driven diselenide metathesis reactions with different types of diselenides are investigated systematically. Their exchange reaction rates and equilibrium conversions are compared in the aspects of the different diselenide structures, activation conditions and solvents. As a result, the metathesis reactions between diselenide small molecules are demonstrated with high dynamic and sensitive features, which can be broadly tuned by varying the electron affinity and aromaticity of the diselenide substituents and external conditions(e.g., solvent, stimulus mode). The current work thus will not only advance our understanding on diselenide metathesis chemistry, but also promote concrete and impactful studies in selenium-containing materials. 相似文献
Adsorptive separation of C2H6 from C2H4 by adsorbents is an energy-efficient and promising method to boost the polymer grades C2H4 production. However, that C2H6 and C2H4 display very similar physical properties, making their separation extremely challenging. In this work, by regulating the pore environment in a family of chitosan-based carbon materials (C-CTS-1, C-CTS-2, C-CTS-4, and C-CTS-6)- we target ultrahigh C2H6 uptake and C2H6/C2H4 separation, which exceeds most benchmark carbon materials. Explicitly, the C2H6 uptake of C-CTS-2 (166 cm3/g at 100 kPa and 298 K) has the second-highest adsorption capacity among all the porous materials. In addition, C-CTS-2 gives C2H6/C2H4 selectivity of 1.75 toward a 1:15 mixture of C2H6/C2H4. Notably, the adsorption enthalpies for C2H6 in C-CTS-2 are low (21.3 kJ/mol), which will facilitate regeneration in mild conditions. Furthermore, C2H6/C2H4 separation performance was confirmed by binary breakthrough experiments. Under different ethane/ethylene ratios, C-CTS-X extracts a low ethane concentration from an ethane/ethylene mixture and produces high-purity C2H4 in one step. Spectroscopic measurement and diffraction analysis provide critical insight into the adsorption/separation mechanism. The nitrogen functional groups on the surface play a vital role in improving C2H6/C2H4 selectivity, and the adsorption capacities depend on the pore size and micropore volume. Moreover, these robust porous materials exhibit outstanding stability (up to 800 °C) and can be easily prepared on a large scale (kg) at a low cost (~$26 per kg), which is very significant for potential industrial applications. 相似文献