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41.
An experimental investigation of flow around a square cylinder placed at various angles with respect to the approach fluid velocity is reported. The focus of the study is toward examining the sensitivity of the wake properties to the cylinder orientation and Reynolds number. Angles of incidence in the range of 0-60° and Reynolds numbers of 1340, 4990, and 9980 have been considered. Velocity measurements have been carried out using an X-wire hotwire anemometer. The Strouhal number and the drag coefficient of the cylinder have been computed from the wake measurements. Utilizing the velocity traces at distinct probe locations in the near and the far wake, statistical properties such as the RMS velocities and the spectra have been obtained. Results obtained in the present work revealed that for a cylinder with zero inclination, flow separates from the corners on the face exposed to the incoming flow. For inclinations greater than zero, the points of separation on the cylinder move downstream and the wake size increases, but the separated shear layer rolls up over a shorter distance. These factors lead to a reduced drag coefficient and a higher Strouhal number. The center-line recovery of the time-averaged velocity and the decay rates of velocity fluctuations depend on the Reynolds number. A marginal effect of the cylinder orientation is also seen.  相似文献   
42.
Nardostachys jatamansi DC. is a highly reputed Medhya and Nootropic (Learning and Memory) Ayurvedic medicinal plant. Its use as herbal medicine singly and as an ingredient of multi‐herbal formulations is fast increasing. In order to authenticate and evaluate it quantitatively, its standardization is highly warranted with respect to a reliable marker. In this connection a rapid and highly sensitive UPLC‐QTOF MS method has been developed. The analysis was carried out on an Acquity BEH C18 column with gradient elution of methanol–water and 3 mm ammonium acetate using QTOF mass detector in negative ionization mode. The method was validated over a concentration range of 9.76–156.25 ng/mL nardin. The calibration curve is linear with the correlation coefficient (r) and coefficient of determination (R2) were 0.9997 and 0.9995 respectively. The LOD and LOQ were 3.050 and 9.277 ng/mL respectively. The recovery of nardin in the range 96.36–111.13% achieved from spiked samples was consistent and reproducible. The inter‐day and intra‐day assay precision of the analytes over the entire concentration range was less than 5%. The developed method required only 4 min for chromatography to authenticate and quantify the marker, viz. nardin in N. jatamansi samples, in addition to the sample preparation time. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   
43.
In this paper, we consider the Galerkin and collocation methods for the eigenvalue problem of a compact integral operator with a smooth kernel using the Legendre polynomials of degree ≤n. We prove that the error bounds for eigenvalues are of the order O(n−2r) and the gap between the spectral subspaces are of the orders O(nr) in L2-norm and O(n1/2−r) in the infinity norm, where r denotes the smoothness of the kernel. By iterating the eigenvectors we show that the iterated eigenvectors converge with the orders of convergence O(n−2r) in both L2-norm and infinity norm. We illustrate our results with numerical examples.  相似文献   
44.
Patent review     
The section on patent review will be focused in the areas of interest to the readers of CCHTS. The search was conducted using the following key words: combinatorial chemistry, high throughput screening, drug repurposing, chemical library, high content screening, drug discovery and natural products. All patents highlighted here are identified by the patent number issued either by the World Intellectual Property Organization or by a regional patent office.  相似文献   
45.
In this paper, sufficient conditions have been obtained for oscillation of all solutions of a class of nonlinear neutral delay difference equations of the form
$ \Delta \left( {r\left( n \right)\Delta \left( {y\left( n \right) + p\left( n \right)y\left( {n - m} \right)} \right)} \right) + q\left( n \right)G\left( {y\left( {n - k} \right)} \right) = 0 $ \Delta \left( {r\left( n \right)\Delta \left( {y\left( n \right) + p\left( n \right)y\left( {n - m} \right)} \right)} \right) + q\left( n \right)G\left( {y\left( {n - k} \right)} \right) = 0   相似文献   
46.
Designs, Codes and Cryptography - Let $${\mathbb {F}}_q$$ denote the finite field of order q,  and let $$n = m_1+m_2+\cdots +m_\ell ,$$ where $$m_1,m_2,\ldots ,m_\ell $$ are arbitrary...  相似文献   
47.
A Liapunov-type inequality for a class of third order delay-differential equations is derived.  相似文献   
48.
Combustion dynamics leading to thermoacoustic instability in a rearward-facing step stabilized premixed flame is experimentally examined with the objective of investigating the fluid dynamic mechanism that drives heat release rate fluctuations, and how it couples with the acoustic field. The field is probed visually, using linear photodiode arrays that capture the spatiotemporal distribution of CH* and OH*; an equivalence ratio monitor; and a number of pressure sensors. Results show resonance between the acoustic quarter wave mode of the combustion tunnel and a fluid dynamic mode of the wake. Under unstable conditions, the flame is convoluted around a large vortex that extends several step heights downstream. During a typical cycle, while the velocity is decreasing, the vortex grows, and the flame extends downstream around its outer edge. As the velocity reaches its minimum, becoming mostly negative, the vortex reaches its maximum size, and the flame collides with the upper wall; its leading edge folds, trapping reactants pockets, and its trailing edge propagates far upstream of the step. In the next phase, while the velocity is increasing, the heat release grows rapidly as trapped reactant’ pockets are consumed by flames converging towards their centers, and the upstream flame is dislodged back downstream. The heat release rate reaches its maximum halfway into the velocity rise period, leading the maximum velocity by about 90°. In this quarter-wave mode, the pressure leads the velocity by 90° as well, that is, it is in phase with the heat release rate. Numerical modeling results support this mechanism. Equivalence ratio contribution to the instability mechanism is shown to be minor, i.e., heat release dynamics are governed by the cyclical formation of the wake vortex and its interaction with the flame.  相似文献   
49.
Kinetics of oxidation of aryl aliphatic ketones by CeIV in presence of HClO4 in aqueous acetic acid medium has been studied. Reactivity has been found to be that substituents of electron withdrawing nature accelerate the reaction and the reverse is true with electron releasing substituents. A mechanism of radical intermediate is postulated to explain the observed phenomena. The unusual reactivity of the alkoxy derivatives may be traced to a change in the mechanism routed through a carbonium ion centre or alternatively it might be due to the hydrolysis of the alkoxy derivatives leading to the higher reactivity observed.  相似文献   
50.
In this investigation an approach to correlate the composite rate constants of some redox polymerization reactions [acrylonitrile-Ce(IV)-organic substrate] with a new type of multiparameter equation is described. The multiparameter equation is based on Swain and Lupton's F and R, the field and resonance components of the substituents, respectively, and the unique positional weighting factors f and r suggested by Williams and Norrington. The statistical parameters of the correlation involving the substituent constants (fF and rR) and the rate data have been found to be quite satisfactory, the average coefficient of determination being 0.91. The significance levels of the correlation also indicate that the present model is applicable to the kinetics of redox polymerization. The sign and magnitude of the reaction-dependent regression constants α and β suggest that three different types of reaction mechanisms are operative for the substrates benzaldehyde, phenylthiourea, acetophenone, and toluene.  相似文献   
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