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本文介绍一种以塑性变形减震概念设计的用于地下爆炸地表层裂区内的仪器车减震台。文中叙述了设计的原理和计算方法。通过同普通的由弹簧和阻尼器构成的减震台的计算对比,说明这种以塑性变形减震概念设计的减震台具有许多优点。对减震台做了吊高达1.5m的落地冲击实验,其结果同计算一致。 相似文献
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We consider a one-dimensional stochastic control problem that arises from queueing network applications. The state process
corresponding to the queue-length process is given by a stochastic differential equation which reflects at the origin. The
controller can choose the drift coefficient which represents the service rate and the buffer size b>0. When the queue length reaches b, the new customers are rejected and this incurs a penalty. There are three types of costs involved: A “control cost” related
to the dynamically controlled service rate, a “congestion cost” which depends on the queue length and a “rejection penalty”
for the rejection of the customers. We consider the problem of minimizing long-term average cost, which is also known as the
ergodic cost criterion. We obtain an optimal drift rate (i.e. an optimal service rate) as well as the optimal buffer size
b
*>0. When the buffer size b>0 is fixed and where there is no congestion cost, this problem is similar to the work in Ata, Harrison and Shepp (Ann. Appl.
Probab. 15, 1145–1160, 2005). Our method is quite different from that of (Ata, Harrison and Shepp (Ann. Appl. Probab. 15, 1145–1160, 2005)). To obtain a solution to the corresponding Hamilton–Jacobi–Bellman (HJB) equation, we analyze a family of ordinary differential
equations. We make use of some specific characteristics of this family of solutions to obtain the optimal buffer size b
*>0.
A.P. Weerasinghe’s research supported by US Army Research Office grant W911NF0510032. 相似文献
128.
InfluenceofBuffer-LayerThicknessonPerformanceofWaveguideModulators¥XAINGYunnan;WANGKuiru;YUGuoxian;XUDaxiong(BeijingUnversity... 相似文献
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The effects of liquid chromatography mobile phase buffer contents on the ionization and fragmentation of drug molecules in liquid chromatographic/ionspray tandem mass spectrometric (LC/MS/MS) determination were evaluated for simvastatin (SV) and its hydroxy acid (SVA). The objective was to improve further the sensitivity for SV by overcoming the unfavorable condition caused by the formation of multiple major adduct ions and multiple major fragment ions when using ammonium as LC mobile phase buffer. Mobile phases (70:30 acetonitrile-buffer, 2 mM, pH 4.5) with buffers made from ammonium, hydrazine or alkyl (methyl, ethyl, dimethyl or trimethyl)-substituted ammonium acetate were evaluated. Q1 scan and product ion scan spectra were obtained for SV in each of the mobile phases under optimized conditions. The results showed that, with the alkylammonium buffers, the alkylammonium-adducted SV was observed as the only major molecular ion, while the formation of other adduct ions ([M + H](+), [M + Na](+) and [M + K](+)) was successfully suppressed. On the other hand, product ion spectra with a single major fragment ion were not observed for any of the alkylammonium-adducted SVs. The affinity of the alkylammoniums to SV and the basicity of the alkylamines are believed to be factors influencing the formation and abundance of molecular and fragment ions, respectively. Methylammonium acetate provided the most favorable condition among all the buffers evaluated and improved the sensitivity several-fold for SV in LC/MS/MS quantitation compared with that obtained using ammonium acetate buffer. Better precision for SV in both Q1 and SRM scans was observed when using methylammonium buffer compared with those using ammonium buffer. The mobile phase buffer contents did not seem to affect the ionization, fragmentation and chromatography of SVA. The results of this evaluation can be applied to similar situations with other organic molecules in ionspray LC/MS/MS determination. 相似文献
130.
M.J.Guiomar H.M Lito M.Filomena G.F.C Camões A.K Covington 《Analytica chimica acta》2003,482(1):137-146
Solutions of potassium dihydrogen citrate, KH2C6H5O7, exhibit reference pH values close to those of the primary standard pH buffer solutions of tartrate and phthate. Nevertheless, as opposed to all other recommended primary buffer standards, the citrate reagent is not commercially available as a standard reference material (SRM).In this work, experiments have been performed on solid reagent from different sources, which revealed the presence of the various citrate species in variable amounts. This may arise from the sensitivity of the system to the purification strategy, owing to the proximity of the acidity constants of the triprotic citric acid, H3C6H5O7.An experimental procedure has been developed which leads to a satisfactory preparation of the citrate reagent, to an extent that its solutions, independently of batch on supplier, exhibit reproducible pH values, in agreement with the conventionally assigned pH (S) = 3.776 at 25 °C for 0.05 m KH2C6H5O7.Comparison of expected and experimental values is used as a quantitative test for the quality of reagent, eventually indicating the need for purification according to recommendations. 相似文献