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排序方式: 共有74条查询结果,搜索用时 15 毫秒
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Llabrés i Xamena FX Teruel L Alvaro M Garcia H 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(2):515-519
We have used porous anodised Al(2)O(3) membranes as inert matrix for constructing and organizing spatially ternary donor/conductor/acceptor (DCA) systems exhibiting photovoltaic cell activity on the micrometric-length scale. These DCA triads were built stepwise by first growing a conducting polymer inside the membrane pores, thus forming nanorods that completely fill the internal pore space of the membrane. Then, an electron donor and an electron acceptor were adsorbed one on each side of the membrane, so that they were separated by a distance equal to the membrane thickness (ca. 60 microm), but electronically connected through the conductive polymer. When this device was placed between two electrodes and irradiated with visible light, electrons jumped from the donor molecule, crossed the membrane from side to side through the conductive polymer (a journey of about 60 microm!) until they finally reach the acceptor molecule. In so doing, an electric voltage was generated between the two electrodes, capable of maintaining an electric current flow from the membrane to an external circuit. Our DCA device constitutes the proof of a novel concept of photovoltaic cells, since it is based on the spatial organization at the micrometric scale of complementary, but not covalently linked, electron-donor and electron-acceptor organic species. Thus, our cell is based in translating photoinduced electron transfer between donors and acceptors, which is known to occur at the molecular nanometric scale, to the micrometric range in a spatially organised system. In addition our cell does not need the use of liquid electrolytes in order to operate, which is one of the main drawbacks in dye-sensitised solar cells. 相似文献
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An experimental study of the thermal decomposition of a β‐hydroxy alkene, 3‐methyl‐3‐buten‐1‐ol, in m‐xylene solution, has been carried out at five different temperatures in the range of 513.15–563.15 K. The temperature dependence of the rate constants for the decomposition of this compound in the corresponding Arrhenius equation is given by ln k (s?1) = (25.65 ± 1.52) ? (17,944 ± 814) (kJ·mol?1)·T?1. A computational study has been carried out at the M05–2X/6–31+G(d,p) level of theory to calculate the rate constants and the activation parameters by the classical transition state theory. There is a good agreement between the experimental and calculated rate constants and activation Gibbs energies. The bonding characteristics of reactant, transition state, and products have been investigated by the natural bond orbital analysis, which provides the natural atomic charges and the Wiberg bond indices. Based on the results obtained, the mechanism proposed is a one‐step process proceeding through a six‐membered cyclic transition state, being a concerted and slightly asynchronous process. The results have been compared with those obtained previously by us (Struct Chem 2013, 24, 1811–1816) for the thermal decomposition of 3‐buten‐1‐ol, in m‐xylene solution. We can conclude that in the compound studied in this work, 3‐methyl‐3‐buten‐1‐ol, the effect of substitution at position 3 by a weakly activating CH3 group is the stabilization of the transition state formed in the reaction and therefore a small increase in the rate of thermal decomposition. 相似文献
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Abstract Due to the wide use of polymers in medicine, researchers are required to solve a very important problem–to understand the interaction between materials of nonphysiological origin and the surrounding biological liquids, and tissues, particularly blood. 相似文献
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Luis M. Romeo Luis I. DíezIsabel Guedea Irene BoleaCarlos Lupiáñez Ana GonzálezJavier Pallarés Enrique Teruel 《Experimental Thermal and Fluid Science》2011,35(3):477-484
Oxyfuel combustion is a promising alternative for CO2 capture. While this has been proven in pulverized fuel (PF) burners, research in fluidized bed (FB) reactors is still scarce. Our work aims to increase the knowledge about this technology. To this purpose, a 95 kWth FB oxyfuel combustion test rig has been erected. Its main characteristics are described in this paper, giving detailed information on the subsystems: the FB reactor, the fuel and oxidant supplies, and ancillaries. Plant flexibility is emphasized. It allows to operate under different CO2/O2 ratios, and to recycle CO2 from the flue gases. Both the processes design and monitoring are supported by simulations that have been validated against experimental data, regarding fluid dynamics, combustion, and heat transfer. Finally, the performance of the facility has been tested both with coal alone and blended with biomass. CO2 concentrations over 90% (dry basis) in the flue gases have been obtained. Comparison of air and oxygen combustion tests and operational recommendations are discussed, confirming the feasibility of the FB oxyfuel technology for CO2 capture purposes. 相似文献
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The rate constant of the reaction of OH radicals with butyl acrylate was studied for the first time using an atmospheric simulation chamber at 298 K and ~750 Torr of air or nitrogen. The decay of the organics was followed using a gas chromatograph with a flame ionization detector (GC‐FID), and the rate constant was determined using a relative rate method with different references. The obtained average value of (1.80 ± 0.26) × 10?11 cm3 molecule?1 s?1 is in agreement with previous determinations of the rate constants of OH radicals with acrylates and methacrylates in the literature. Additionally, product identification under atmospheric conditions was performed for the first time by the GC‐MS technique. Butyl glyoxalate was observed as the degradation product in accordance with the addition of OH to the less substituted carbon atom of the double bond, followed by decomposition of the 1,2‐hydroxyalkoxy radicals formed. Room temperature rate coefficient was used to estimate the atmospheric lifetime of the ester studied. Reactivity trends are discussed in terms of the substituent effects and the length of the hydrogenated chain of the ester. The atmospheric persistence of BUAC was calculated taking into account the experimental rate constant obtained. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
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José Angel Brito Helena Teruel Stéphane Massou Montserrat Gómez 《Magnetic resonance in chemistry : MRC》2009,47(7):573-577
Oxomolybdenum(VI) complexes containing diverse ligands from an electronic and topological point of view have been analysed by means of 95Mo NMR in solution with the purpose of using this technique as a tool to study their coordination chemistry and reactivity. The relationship between the electronic density on the metal tuned by the electron‐donor ability of the coordinated ligands and the 95Mo chemical shift has been proved for mono‐ and bimetallic complexes showing a hexa‐ or hepta‐coordination around the metal centre. The different origins of the signal broadening (associated either to the symmetry of the metallic polyhedron or to the presence of isomers or to the ligand de‐coordination) have been also considered to rationalise the obtained data. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
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José A. Gálvez Antonio Martínez José L. Teruel 《Journal of Mathematical Analysis and Applications》2014
The paper deals with the study of complete embedded flat surfaces in H3 with a finite number of isolated singularities. We give a detailed information about its topology, conformal type and metric properties. We show how to solve the generalized Weyl?s problem of realizing isometrically any complete flat metric with Euclidean singularities in H3 which gives the existence of complete embedded flat surfaces with a finite arbitrary number of isolated singularities. 相似文献