A hydrometallurgical route based on leaching-crystallization steps for the separation of metals Al, Co, Cu and Li from spent Li-ion batteries was evaluated in this paper. Once dismantled for the removal of both plastic and steel cases, the anode (containing mainly Cu) of such batteries was manually separated from the cathode (which contains Al, Co and Li) for the recovery of Cu. The metal content of both anode and cathode was assessed by X-ray diffraction (XRD), X-ray fluorescence (XRF) and atomic absorption analytical methods. The cathode was firstly leached with NaOH for the selective removal of Al, followed by leaching with H2SO4 + H2O2 for the dissolution of the remaining Co and Li. The operating variables concentration of NaOH and concentration of H2O2 were found significant for the metal dissolution conditions investigated at basic and acid leaching operations, respectively. On the other hand, the variables temperature and concentration of H2SO4 showed minor effects at acid leaching step. Reaction schemes were proposed to describe basic and acid leaching operations. The recovery of Co from the acid liquor was carried out by crystallization. This hydrometallurgical route was found to be simple and adequate to separate metals for recycling purposes. 相似文献
A metal Fischer carbene [(CO)5WC(φ)OCH2CH3] was covalently linked for the first time to the silanol groups of the mesoporous channels of SBA15 by following two different synthetic anchoring routes. The first one goes through the reaction of the SBA15 mesoporous silica walls functionalized by aminopropyltriethoxysilane (APTES) with a tungsten carbene Wφ, while in the second approach a precursor synthesized by reacting APTES with the carbene Wφ is then anchored via a direct bond to the silanol groups in the interior pore channels of SBA-15.
This tethering is helpful to prevent the decomposition of the metallic complex. XRD, N2 adsorption–desorption, and TEM analysis provide strong evidence that the mesoporous support structure retains its long-range ordering after the grafting process, despite a significant reduction of its specific surface area, pore-volume and pore-size. The chemical bonding of the tungsten carbene to the silanol groups of SBA-15 materials was studied with solid-state NMR spectroscopy. Both 13C MAS NMR and 29Si CP MAS NMR spectra confirm the covalent linking of the carbene to the silica-pore system. 相似文献
N-Acylphosphatidylserines have been isolated from intact and injured tissues, but the participation of such acidic phospholipids
in membrane aggregation and fusion has not been demonstrated. We have synthesized N-stearoylphosphatidylserine (NSPS) and examined divalent-cation-induced aggregation of NSPS-liposomes, which leads to membrane
destabilization and fusion. The purified lipid was characterized by its chromatographic and spectroscopic (infrared and 1H nuclear magnetic resonance) properties and by its chemical degradation pattern. Aggregation of unilamellar NSPS-liposomes
was studied as a function of calcium and magnesium concentration. The ability of calcium and magnesium to induce vesicle aggregation
is higher for phosphatidylserine (PS)-liposomes (threshold concentration 1.5 mM for calcium and 4.6 mM for magnesium) than
for NSPS-liposomes (threshold concentration 2.8 mM for calcium and 6.6 mM for magnesium). The irreversibility of the aggregation
reactions after adding EDTA suggests that vesicle fusion might occur in the presence of calcium and magnesium. Preliminary
studies, based on mixing of both lipid and internal aqueous contents, show that fusion rather than aggregation of NSPS-liposomes
occurs in the presence of calcium ions. The tendency of NSPS-liposomes to aggregate at higher cation concentrations than PS-liposomes
suggests that N-acylation of phosphatidylserine protects the membrane against degenerative damage caused by aggregation and fusion. 相似文献
Herein we describe a class of unconventional nucleosides (methyloxynucleosides) that combine unconventional nucleobases such as substituted aminopyrimidines, aminopurines, or aminotriazines with unusual sugars in their structures. The allitollyl or altritollyl derivatives were pursued as ribonucleoside mimics, whereas the tetrahydrofuran analogues were pursued as their dideoxynucleoside analogues. The compounds showed poor, if any, activity against a broad range of RNA and DNA viruses, including human immunodeficiency virus (HIV). This inactivity may be due to lack of an efficient metabolic conversion into their corresponding 5′‐triphosphates and poor affinity for their target enzymes (DNA/RNA polymerases). Several compounds showed cytostatic activity against proliferating human CD4+ T‐lymphocyte CEM cells and against several other tumor cell lines, including murine leukemia L1210 and human prostate PC3, kidney CAKI‐1, and cervical carcinoma HeLa cells. A few compounds were inhibitory to Moloney murine sarcoma virus (MSV) in C3H/3T3 cell cultures, with the 2,6‐diaminotri‐O‐benzyl‐D ‐allitolyl‐ and ‐D ‐altritolyl pyrimidine analogues being the most potent among them. This series of unconventional nucleosides may represent a novel family of potential antiproliferative agents. 相似文献
Commercial gold nanoparticles supported on titanium dioxide (TiO2) were found to be a highly efficient catalyst for alkyne hydroamination. Terminal alkynes could easily undergo intermolecular hydroamination with low catalyst loadings (0.2 mol% Au) under solvent‐free conditions. Indoles were efficiently synthesized using microwave heating through intramolecular hydroamination.
Sub-micrometer powder (100–150 nm diameter) of Yb-doped yttrium oxide was obtained, for the first time, by microwave-assisted polyol (diethylene glycol, DEG) method. This method is based on fast and homogeneous increase of temperature, due to the microwave heating, and on addition of the hydrolysing agent (water) at high temperature. This promotes a fast nucleation followed by a controlled growth of nuclei. Different procedures were used to process the as-synthesized powders. In some cases washing by ultrapure water was used to dissolve nitrate and DEG by-products, this treatment allowed the use of a lower calcination temperature (150–200 °C less) to obtain the crystalline phase. Analysis of the calcined powder showed different levels of structures: from nanocrystal (10–15 nm), to primary particles (100–150 nm), to micrometer soft aggregates (2–4 μm). The microwave-assisted polyol method resulted an easy way to dope yttria with the desired amount of Yb3+. This work was carried out in order to prepare particles to be used as rare-earth doped Y2O3 and YAG polycrystalline transparent ceramic for laser source applications. 相似文献