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121.
122.
A method is presented for the continuous analysis of generated vapors of the nerve agents soman and sarin and the blistering agent sulfur mustard. By using a gas sampling valve and a very short (15 cm) column connected to an on-column injector with a “standard length” column, the system can either be calibrated or used for performing high speed gas analyses. When using a flame ionization detector, the detection limit was ca. 100 ppb (ca. 0.5–1.0 mg/m3). This technique is applied in inhalation toxicokinetic studies of nerve agents and mustard gas in the guinea pig.  相似文献   
123.
We discuss synchronization in networks of neuronal oscillators which are interconnected via diffusive coupling, i.e. linearly coupled via gap junctions. In particular, we present sufficient conditions for synchronization in these networks using the theory of semi-passive and passive systems. We show that the conductance based neuronal models of Hodgkin-Huxley, Morris-Lecar, and the popular reduced models of FitzHugh-Nagumo and Hindmarsh-Rose all satisfy a semi-passivity property, i.e. that is the state trajectories of such a model remain oscillatory but bounded provided that the supplied (electrical) energy is bounded. As a result, for a wide range of coupling configurations, networks of these oscillators are guaranteed to possess ultimately bounded solutions. Moreover, we demonstrate that when the coupling is strong enough the oscillators become synchronized. Our theoretical conclusions are confirmed by computer simulations with coupled Hindmarsh-Rose and Morris-Lecar oscillators. Finally we discuss possible “instabilities” in networks of oscillators induced by the diffusive coupling.  相似文献   
124.
125.
Internationally distributed organic and inorganic oxygen isotopic reference materials have been calibrated by six laboratories carrying out more than 5300 measurements using a variety of high‐temperature conversion techniques (HTC) a in an evaluation sponsored by the International Union of Pure and Applied Chemistry (IUPAC). To aid in the calibration of these reference materials, which span more than 125‰, an artificially enriched reference water (δ18O of +78.91‰) and two barium sulfates (one depleted and one enriched in 18O) were prepared and calibrated relative to VSMOW2 b and SLAP reference waters. These materials were used to calibrate the other isotopic reference materials in this study, which yielded:
Reference material δ18O and estimated combined uncertainty c
IAEA‐602 benzoic acid +71.28 ± 0.36‰
USGS35 sodium nitrate +56.81 ± 0.31‰
IAEA‐NO‐3 potassium nitrate +25.32 ± 0.29‰
IAEA‐601 benzoic acid +23.14 ± 0.19‰
IAEA‐SO‐5 barium sulfate +12.13 ± 0.33‰
NBS 127 barium sulfate +8.59 ± 0.26‰
VSMOW2 water 0‰
IAEA‐600 caffeine ?3.48 ± 0.53‰
IAEA‐SO‐6 barium sulfate ?11.35 ± 0.31‰
USGS34 potassium nitrate ?27.78 ± 0.37‰
SLAP water ?55.5‰
The seemingly large estimated combined uncertainties arise from differences in instrumentation and methodology and difficulty in accounting for all measurement bias. They are composed of the 3‐fold standard errors directly calculated from the measurements and provision for systematic errors discussed in this paper. A primary conclusion of this study is that nitrate samples analyzed for δ18O should be analyzed with internationally distributed isotopic nitrates, and likewise for sulfates and organics. Authors reporting relative differences of oxygen‐isotope ratios (δ18O) of nitrates, sulfates, or organic material should explicitly state in their reports the δ18O values of two or more internationally distributed nitrates (USGS34, IAEA‐NO‐3, and USGS35), sulfates (IAEA‐SO‐5, IAEA‐SO‐6, and NBS 127), or organic material (IAEA‐601 benzoic acid, IAEA‐602 benzoic acid, and IAEA‐600 caffeine), as appropriate to the material being analyzed, had these reference materials been analyzed with unknowns. This procedure ensures that readers will be able to normalize the δ18O values at a later time should it become necessary. The high‐temperature reduction technique for analyzing δ18O and δ2H is not as widely applicable as the well‐established combustion technique for carbon and nitrogen stable isotope determination. To obtain the most reliable stable isotope data, materials should be treated in an identical fashion; within the same sequence of analyses, samples should be compared with working reference materials that are as similar in nature and in isotopic composition as feasible. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   
126.

Turbulent-flow chromatography (TFC) on-line coupled to liquid chromatography mass spectrometry (LC-MS) is used to determine flavonoids and resveratrol in different types of wines. A fully automated system was developed in which 10 mL of sample (diluted wine) was passed over a TFC column, after which the retained analytes were separated by reversed-phase LC and detected by negative ion mode atmospheric-pressure chemical ionization (APCI) MS. The method proved to be fast, non-laborious, robust and sensitive. The feasibility of the method was tested on several red, white and rose wines. Quantitation of resveratrol was possible using the standard addition procedure. Red wine showed the highest amount of resveratrol (4 mg L−1), while rose and white wine contained concentrations which were about ten fold lower.

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127.
Let , and be linear spaces and let A and B be linear relations from to and from to , respectively. The main result of this note is a formula which relates the nullities and the defects of the relations A and B with those of the product relation BA.  相似文献   
128.
Kre?n's formula provides a parametrization of the generalized resolvents and Štraus extensions of a closed symmetric operator with equal possibly infinite defect numbers in a Hilbert space in terms of Nevanlinna families in a parameter space. The aim of this note is to give a simple complete analytical proof of Kre?n's formula.  相似文献   
129.
We examine a recolouring scheme ostensibly used to assist in classifying geographic data. Given a drawing of a graph with bi-chromatic points, where the points are the vertices of the graph, a point can be recoloured if it is surrounded by neighbours of the opposite colour. The notion of surrounded is defined as a contiguous subset of neighbours that span an angle greater than 180 degrees. The recolouring of surrounded points continues in sequence, in no particular order, until no point remains surrounded. We show that for some classes of graphs the process terminates in a polynomial number of steps. On the other hand, there are classes of graphs with infinite recolouring sequences.  相似文献   
130.
The spin-crossover complex [Fe(teec)(6)](ClO(4))(2) (teec = chloroethyltetrazole) exhibits a 50 % incomplete spin crossover in the temperature range 300-30 K. Time-resolved synchrotron powder diffraction experiments have been carried out to elucidate its structural behavior. We report crystal structure models of this material at 300 K (high spin) and 90 K (low spin), as solved from synchrotron powder diffraction data by using Genetic Algorithm and Parallel Tempering techniques and refined with Rietveld refinement. During short synchrotron powder diffraction experiments (five minutes duration) two distinguishable lattices were observed the quantities of which vary with temperature. The implication of this phenomenon, that is interpreted as a structural phase transition associated with the high-to-low spin crossover, and the structural characteristics of the high-spin and low-spin models are discussed in relation to other compounds showing a similar type of spin-crossover behavior.  相似文献   
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