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排序方式: 共有70条查询结果,搜索用时 171 毫秒
1.
Marianny Yajaira Combariza Cristian Blanco Tirado Elena Stashenko Takayuki Shibamoto 《Journal of separation science》1994,17(9):643-646
The dependence of the limonene content of lemon (Citrus volkameriana) peel oil on the degree of ripeness of the fruit has been studied by using steam distillation and cold pressing to extract the oils from lemon fruit peel at different stages of maturation (green, greenish-yellow, and yellow-orange peel coloration). Samples of essential oils were analyzed by high resolution GC and GC-MS, using tetradecane as internal standard for quantitation. Forty components were detected; thirty eight were positively identified by comparison of their mass spectra (El, 70 eV) and Kováts retention indexes (determined using a non-logarithmic scale on capillary columns coated with both polar (DB-Wax) and non-polar (DB-1) stationary phases) with those of standards and with data reported in the literature. The limonene concentration reached a maximum level of 79.4% when the fruit was in the intermediate maturation stage characterized by greenish-yellow coloration. 相似文献
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A. Concheso R. Santamaría R. Menéndez J. M. Jiménez-Mateos R. Alcántara P. Lavela J. L. Tirado 《Journal of Solid State Electrochemistry》2005,9(9):627-633
The effect of oxidative stabilization as a mean to modify the carbon texture was essayed in a group of mesophases previous to carbonization at 900 °C with the aim of evaluating the influence on electrochemical performance when used as electrode materials in lithium test cells. X-ray diffraction, optical microscopy and chemical analysis, Fourier-transform infrared spectroscopy have been used to describe the compositional and textural properties of the as-produced parent mesophases, the samples were further treated under air current to stabilize their microstructures and the corresponding carbonized samples at 900 °C. The electrochemical performance was determined by the galvanostatic method and further correlated to the physical–chemical properties and interface resistance of the materials. In all cases, the stabilization process has demonstrated a beneficial effect on the capacity retention in the measured range. 相似文献
4.
Ricardo Alcántara Pedro Lavela Gregorio Ortiz Inés Rodríguez José L. Tirado 《Hyperfine Interactions》2008,187(1-3):13-17
Cobalt–tin intermetallic compounds with different particle size have been obtained and characterized by using 119Sn Mössbauer spectroscopy as a main tool. The electrochemical behavior of the Co–Sn compounds has been evaluated in lithium test cells. The Lamb–Mössbauer factors for CoSn with different crystallite sizes have been calculated. The results f nano???CoSn(300 K) = 0.19 and f coarse???CoSn(300 K) = 0.55 are obtained. Nano-CoSn exhibits larger capacity to react with lithium than coarse-CoSn. 相似文献
5.
Tin oxalate as a precursor of tin dioxide and electrode materials for lithium-ion batteries 总被引:2,自引:0,他引:2
R. Alcántara Fernández F. Madrigal P. Lavela C. Pérez-Vicente J. Tirado 《Journal of Solid State Electrochemistry》2001,6(1):55-62
Tin(II) oxalate was studied as a novel precursor for active electrode materials in lithium-ion batteries. The discharge of
lithium cells using tin oxalate electrodes takes place by three irreversible steps: tin reduction, forming a lithium oxalate
matrix; solvent decomposition to form a passivating layer; and oxalate reduction in a two-electron process. These are followed
by reversible alloying of tin with lithium, leading to a maximum discharge of 11 F/mol. Cycling of the cells showed reversible
capacities higher than 600 mAh/g during the first five cycles and ca. 200 mAh/g after 50 cycles. Tin oxalate was converted
to tin dioxide by thermal decomposition at 450 °C and also by a chemical method by dissolving tin oxalate powder in 33% v/v
hydrogen peroxide at room temperature. The ultrafine nature of the tin dioxide powders obtained by this procedure allow their
use as electrodes in lithium cells. The best capacity retention during the first five cycles was achieved for a sample heat
treated to 250 °C to eliminate surface water.
Electronic Publication 相似文献
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Organozinc reagents FG-(CH2)nZnX containing electrophilic centers (FG) upon conversion to their corresponding zincates (FG-(CH2)nZnMe2Li) and in the presence of 5–8 mol % MeCu(CN)Li, undergo 1,4-additions to cyclic conjugated enones. The intermediate zinc enolates can be trapped with aldehydes to afford products of three-component couplings. 相似文献
9.
E. Zhecheva R. Stoyanova M. Gorova F. R. Alcantara J. Morales J. -L. Tirado 《Ionics》1997,3(1-2):1-15
A new method for the preparation of ultrafine LiCoO2 with a layered crystal structure was developed, which consists in thermal pyrolysis of homogeneous lithium-cobalt-citrate
precursors. Atomic scale mixing of Li and Co is achieved by citric acid acting as a chelating agent. Electron spectroscopy
of concentrated Li-Co-citrate solutions with Li:Co:Cit=1:1:1 and Li:Co:Cit=1:1:2 reveals that the predominant species at pH=7
are [Co(C6H5O7)]− and [Co(C6H5O7)2]4− complexes. Freeze-drying of the two types of solutions leads to the formation of LiCo(C6H5O7).nH2O and (NH4)3LiCo(C6H5O7)2.nH2O precursors, where Co2+ ions are complexed by one and two triionized citrate ions, respectively, and Li+ ions serve as counter ions. Between 400–600 °C, the thermal decomposition of these metal-citrate precursors yields LiCoO2 with layered and pseudo-spinel structure, the proportion between them being depending on: (i) the Co/citrate ratio; (ii)
the concentration of the freeze-dried solution; (iii) the heating rate. At 400 °C, the most defectless layered LiCoO2, consisting of hexagonal individual particles with dimensions of 120–170 nm, is a product of the bis-citrate decomposition
with a slow heating rate. For this sample, heating up to 600 °C does not affect the crystal size dimensions. For ultrafine
layered LiCoO2 and LiCoO2 obtained by solid state reaction at high-temperatures (850 °C), the deintercalation and intercalation reactions proceed in
the 3.95 – 3.99 and 3.86 – 3.88 voltage intervals, respectively. For defect trigonal LiCoO2, additional oxidation and reduction peaks at 3.7 – 3.8 and 3.4 – 3.5 V were observed. We did not succeed in preparing monophase
LiCoO2 with pseudo-spinel structure.
Paper presented at the 3rd Euroconference on Solid State Ionics, Teulada, Sardinia, Sept. 14–21, 1996 相似文献
10.
The variation of crystallite size and microstrains in Co3O4 derived from the thermal decomposition of CoOOH and Co(OH)2 is studied by X-ray diffraction line broadening analysis in several crystallographic directions. The results show that the low-temperature oxide derived from CoOOH produces lower crystallite size and microstrains, due to the development of cracks in the particles instead of a porous system which is characteristic of the sample derived from Co(OH)2. On the other hand, microstrains decrease and crystallite size increases with temperature for both parent compounds, but the changes are dependent on the crystallographic direction. The shape of crystallites is anisotropic at low temperature but the isotropy increases on heating, specially for the samples obtained from CoOOH. 相似文献