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71.
Carvalho Andrade Carolina M. M. Aguiar Wilson Bucker Antranikian Garo 《Applied biochemistry and biotechnology》2001,91(1-9):655-669
Xylanases (EC3.2.1.8) catalyze the hydrolysis of xylan, the major constituent of hemicellulose. The use of these enzymes could
greatly improve the overall economics of processing lignocellulosic materials for the generation of liquid fuels and chemicals.
The hyperthermophilic archaeon Pyrodictium abyssi, which was originally isolated from marine hot abyssal sites, grows optimally at 97°C and is a prospective source of highly
thermostable xylanase. Its endoxylanase was shown to be highly thermostable (over 100 m in at 105°C) and active even at 110°C.
The growth of the deep-sea archaeon P. abyssi was investigated using different culture techniques. Among the carbohydrates used, beech wood xylan, birch wood glucuronoxylan
and the arabinoxylan from oats pelt appeared to be good inducers for endoxylanase and β-xylosidase production. The highest
production of arabinofuranosidase, however, was detected in the cell extracts after growth on xylose and pyruvate, indicating
that the intermediate of the tricarboxylic acid cycle acted as a nonrepressing carbon source for the production of thi enzyme.
Electron microscopic studies did not show a significant difference in the cell surface (e.g., xylanosomes) when P. abyssi cells were grown on different carbohydrates. The main kinetic parameters of the organism have been determined. The cell yield
was shown to be very low owing to incomplete substrate utilization, but a very high maximal specific growth rate was determined
(μmax=0.0195) at 90°C and pH 6.0. We also give information on the problems that arise during the fermentation of this hyperthermophilic
archaeon at elevated temperatures. 相似文献
72.
Alexandre Carlos Camacho Rodrigues José Luiz Fontes Monteiro 《Journal of Thermal Analysis and Calorimetry》2013,111(2):1297-1302
The effect of the calcination procedure on the decomposition of the [Pt(NH3)4]2+ complex in a cesium-containing NaX zeolite was studied by thermal decomposition accompanied by mass spectrometry and diffuse reflectance spectroscopy, as well as electron paramagnetic resonance and infrared spectroscopy. The decomposition of the complex took place in two steps. Under oxygen, the [Pt(NH3)4]2+ complex was first converted into the [Pt(NH3)2]2+ complex in the first step, with predominant nitrogen release. In the second step, corresponding to the decomposition of the remaining two amine ligands, NO was also formed and adsorbed. Oxygen paramagnetic species were also observed. Under He, the decomposition also occurred in two steps with H2 release. 相似文献
73.
Ana Margarida Monteiro Reha H. Tütüncü Luís N. Vicente 《European Journal of Operational Research》2008
We present a new approach to estimate the risk-neutral probability density function (pdf) of the future prices of an underlying asset from the prices of options written on the asset. The estimation is carried out in the space of cubic spline functions, yielding appropriate smoothness. The resulting optimization problem, used to invert the data and determine the corresponding density function, is a convex quadratic or semidefinite programming problem, depending on the formulation. Both of these problems can be efficiently solved by numerical optimization software. 相似文献
74.
Ibon Alkorta Fernando Blanco Pere M. Deyà José Elguero Carolina Estarellas Antonio Frontera David Quiñonero 《Theoretical chemistry accounts》2010,126(1-2):1-14
This review covers two aspects concerning cooperativity in multiple weak bonds: a summary of literature results and a theoretical study of a complete series of model complexes. All the 15 combination of five weak bonds were explored: hydrogen bonds, hydric bonds, dihydrogen bonds, halogen bonds and ion–π interactions. Since in several cases there were no examples reported, a systematic exploration has been carried out on simple models at the MP2/aug-cc-pVTZ level. The results thus obtained have been analyzed using the atoms in molecules methodology. 相似文献
75.
Daria E. Lonsdale Michael R. Whittaker Michael J. Monteiro 《Journal of polymer science. Part A, Polymer chemistry》2009,47(22):6292-6303
Five polymeric architectures with a systematic increase in architectural complexity were synthesized by “click” reactions from a toolbox of functional linear polymers and small molecule linkers. The amphiphilic architectures ranged from a simple 3‐miktoarm star block copolymer to the more complex third generation dendrimer‐like block copolymer, consisting of polystyrene (PSTY) and polyacrylic acid (PAA). Micellization of these architectures in water at a pH of 7 under identical ionic strength gave spherical micelles ranging in size from 9 to 30 nm. Subsequent calculations of the PSTY core density, average surface area per PAA arm on the corona‐core interface, and the relative stretching of the PAA arms provided insights into the effect of architecture on the self‐assembly processes. A particular trend was observed that with increased architectural complexity the hydrodynamic diameter, radius of the core in the dry state and the aggregation number also increased with the exception of the third generation dendrimer. On the basis of these observations, we postulate that thermodynamic factors controlling self‐assembly were the entropic penalty of forming PSTY loops in the core counterbalanced by the reduction in repulsive forces through chain stretching. This results in a greater number of aggregating unimers and consequently larger micelle sizes. The junction points within the architecture also play an important role in controlling the self‐assembly process. The G3 dendrimer showed results contradictory to the aforementioned trend. We believe that the self‐assembly process of this architecture was dominated by the increased attractive forces due to stretching of the PSTY core chains to form a more compact core. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 6292–6303, 2009 相似文献
76.
William Layton Carolina C. Manica Monika Neda Leo G. Rebholz 《Numerical Methods for Partial Differential Equations》2008,24(2):555-582
We study a computationally attractive algorithm (based on an extrapolated Crank‐Nicolson method) for a recently proposed family of high accuracy turbulence models, the Leray‐deconvolution family. First we prove convergence of the algorithm to the solution of the Navier‐Stokes equations and delineate its (optimal) accuracy. Numerical experiments are presented which confirm the convergence theory. Our 3d experiments also give a careful comparison of various related approaches. They show the combination of the Leray‐deconvolution regularization with the extrapolated Crank‐Nicolson method can be more accurate at higher Reynolds number that the classical extrapolated trapezoidal method of Baker (Report, Harvard University, 1976). We also show the higher order Leray‐deconvolution models (e.g. N = 1,2,3) have greater accuracy than the N = 0 case of the Leray‐α model. Numerical experiments for the 2d step problem are also successfully investigated. Around the critical Reynolds number, the low order models inhibit vortex shedding behind the step. The higher order models, correctly, do not. To estimate the complexity of using Leray‐deconvolution models for turbulent flow simulations we estimate the models' microscale.© 2007 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq, 2008 相似文献
77.
Gian Paulo G. Freschi Carolina D. Freschi José A. Gomes Neto 《Mikrochimica acta》2008,161(1-2):129-135
Different kinds of modifiers and coatings on the integrated platform of transversely heated graphite atomizer (THGA) have
been tested for the simultaneous determination of two group of elements: the first, the more volatile, formed by arsenic,
bismuth, lead, antimony and selenium; the second, the less volatile, formed by cobalt, chromium, cupper, iron and manganese
in milk by electrothermal atomic absorption spectrometry. Different Rh-modifiers were studied, such as Rh-coated platforms
(Rh), carbide plus rhodium coated platforms (W-Rh, Zr-Rh), carbide-coated platforms (W and Zr) with co-injection of RhCl3, solutions and uncoated platforms with injection of solutions of Pd(NO3)2, Mg(NO3)2, and RhCl3. Milk samples were diluted 1:10 in 1.0% HNO3 and injected into the tube. The mass of modifier deposited and co-injected in the tube and the use of end capped tubes were
also evaluated in order to improve the electrothermal behavior of analytes. Integrated platform pretreated with W plus co-injection
RhCl3 for first group and pretreated with W-Rh for second group were elected. For 20 μL injected samples the analytical curves
in the 5.0–20.0 μg L−1 concentration range have good linear correlation coefficients (r > 0.998). Relative standard deviations (n = 12) are <6% and the calculated characteristic masses are between 5 pg and 62 pg.
Correspondence: Gian Paulo G. Freschi, Faculdade de Ciências Exatas e Tecnologia, Universidade Federal da Grande Dourados,
PO Box 332, 79.804-970, Dourados-MS, Brazil; Instituto de Química, Universidade Estadual Paulista, PO Box 355, 14801-970 Araraquara-SP,
Brazil 相似文献
78.
79.
Julia Torres Patricia Santos Carolina Ferrari Carlos Kremer Eduardo Kremer 《Journal of solution chemistry》2017,46(12):2231-2247
The interaction of arsenic(V) and arsenic(III) oxyanions with metal cations was investigated by potentiometry under temperature and ionic strength conditions approaching those prevailing in natural waters. The selection includes the major metal cations and some other ions of high environmental relevance. Ionic pairs [M(AsVO4)]?, [M(HAsVO4)] and [M(H2AsIIIO3)]+ formation is suggested for all +2 metal cations, based on the potentiometric results. These ion-pairs between arsenic anions and other metal cations are hardly ever mentioned or taken into account when arsenic speciation in natural waters is considered. These results provide the basis for studying arsenic speciation in natural aquatic systems, on which environmental fate, bioavailability and toxicity of the element depend. Some extrapolations to the conditions of the natural waters are presented as well as some insights into the adsorption process onto hydrous oxides. 相似文献
80.
Carolina G. Dos Santos Daniela T. Marquez Charles-Oneil L. Crites Jose Carlos Netto-Ferreira Juan C. Scaiano 《Tetrahedron letters》2017,58(5):427-431
Two different hybrid materials composed of gold nanoparticles (AuNPs) supported on either commercial niobium oxide HY 340 or mesoporous niobium oxide catalyzed the Friedel-Crafts alkylation of anisole by benzyl chloride. Excitation of the surface plasmon of the supported AuNPs allowed the reaction to occur at lower temperatures by acting as an alternative heat source. The localized heating produced via plasmon excitation permitted the acid catalyzed reaction to occur - at the Lewis acid sites on the Nb2O5 support - at 80 °C while thermal-dark reactions using a conventional heat source, required temperatures of 120 °C or higher. The catalytic activity of the tested hybrid materials decreased with storage time. However, the deactivation showed to be reversible upon lyophilisation indicating that the nature of the deactivation could be due to water adsorption. 相似文献