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401.
Using agents for solving a multi-commodity-flow problem   总被引:1,自引:0,他引:1  
We investigate a commodity trading problem in a flow network with arbitrary topology where sinks combine commodities into bundles in order to generate profits. Our focus is the profit maximization problem for the trading network under both central and distributed control. We compute solutions for the central control problem using an integer linear program while we compute solutions for the distributed case by implementing the nodes in the network as software-agents that exchange messages in order to establish profitable trades. We report on computational results using both methods and demonstrate that there is a connection between agent profits and a centrality measure developed for the problem. We also demonstrate that with our current agent strategy, there is a trade-off between the agents acting too quickly before enough information is available and waiting too long and thus giving each agent too much information and thus too much power over the outcome.  相似文献   
402.
Studies directed at the synthesis of lamellarin G trimethyl ether and ningalin B via vinylogous iminium salt derivatives are described. The successful strategy relies on the formation of a 2,4-disubstituted pyrrole or a 1,2,3,4-tetrasubstituted pyrrole from a vinylogous iminium salt or vinylogous iminium salt derivative. Subsequent transformations of these highly substituted pyrroles lead to efficient and regiocontrolled formal syntheses of the respective pyrrole containing natural products.  相似文献   
403.
Photoneutron spectra around an 18 MV LINAC were calculated in order to observe the effect produced by media around the accelerator. Calculations were carried out with MCNP 4C code, three different cases were analyzed: Head model, Head and phantom model, and Head, air, phantom and wall model. The spectra were calculated in five detectors located at the irradiation room at different distances from the isocentre. A sixth detector, located near the entrance door was included to analyze how the maze change the neutron spectrum. Neutrons are mainly produced in the LINAC head change the shape of evaporation neutrons from the source term, some of these neutrons leak out the head with lesser energy, another neutrons goes with the treatment beam. At any site near the isocentre neutron spectrum has evaporation and thermal neutrons joined by a set of epithermal neutrons. As the distance from the isocentre increases evaporation neutrons tend to decrease while, epithermal and thermal neutrons tend to remain constant regardless de distance due to room return produced by the walls. The maze contributes to reduce the neutron fluence, reducing the evaporation neutrons; resulting spectrum is mainly the contribution of thermal and epithermal neutrons. Near the door these neutrons can produce activation and prompt gamma rays.  相似文献   
404.
It has been already three decades, since the fluorescent nanocrystals called quantum dots (QDs) appeared and attracted attention of a broad scientific community. Their excellent not only optical but also electronic properties predetermined QDs for utilization in a variety of areas. Besides lasers, solar cells, and/or computers, QDs have established themselves in the field of (bio)chemical labeling as well as medical imaging. However, due to the numerous application possibilities of QDs, there are high demands on their properties that need to be precisely controlled and characterized. CE with its versatile modes and possibilities of detection was found to be an effective tool not only for characterization of QDs size and/or surface properties but also for monitoring of their interactions with other molecules of interest. In this minireview, we are giving short insight in analysis of QDs by CE, and summarizing the advantages of this method for QDs characterization.  相似文献   
405.
Using Monte Carlo methods a polyethylene moderator has been designed to induce activation using the photoneutrons field of a 15 MV linear accelerator for radiotherapy. In the calculations the photoneutron spectrum at 1 m from the isocenter was used as a source term and the neutron spectra were calculated in the center of different size cylindrical moderators. The best size was selected defining the thermal-to-fast-neutron ratios as a figure of merit. The moderator was built and its performance was evaluated by inducing the activation of Mn dissolved in water, silver coins and souvenir coin. The thermal neutron fluence rate was determined with the Mn samples being 9.96 × 105 cm?2 Gy x ?1 .  相似文献   
406.
This study aims at the possibility of single structured paramagnetic microparticles (PMPs), composed of maghemite (γ-Fe2O3) core modified with chitosan called MAN8, or tetraethyl orthosilicate covered with Dowex called MAN35, to be helpful for isolation of biogenic amines prior to their further analysis. Primarily, we synthesized and characterized PMPs. To obtain the information about bead morphology, scanning electron microscopy was employed. Furthermore, X-ray fluorescence was employed to carry out the elemental composition analyses. To obtain further insight into interaction between PMP surface and biogenic amines, scanning electron microscope was employed. It was shown that binding of biogenic amines causes increase of relative current response of deprotonated microparticles. We tested the specificity of PMPs to bind biogenic amines on histamine, tyramine, spermine, spermidine, putrescine, and cadaverine. We found that two types of our PMPs were able to selectively bind spermidine, cadaverine, and histamine in the case of MAN35; and histamine, tyramine, and putrescine in the case of MAN8. Finally, we carried out the analyses of real samples obtained from patients suffering from prostate carcinoma, where histamine was determined as the most abundant biogenic amine (10.456–13.654 µg mL?1). The prepared PMPs were able to isolate the biogenic amines from real samples, and thus they may be helpful in construction of biosensors, or Lab-on-a-Chip platforms, enabling less painful, and more rapid diagnosis of prostate cancer.  相似文献   
407.

In order to enhance the sensitivity and to develop a faster direct method for plasma and urine quantification of racemic ketorolac, its metabolites (p-hydroxy-ketorolac and ketorolac glucuronides) and ketorolac enantiomers, we developed an extraction procedure based on solid-phase extraction combined with specific and fast chromatographic separation. Extraction and chromatography resulted in cleaner chromatograms without interfering compounds. In both plasma and urine, linearity of the standard curves for racemic ketorolac and p-hydroxy-ketorolac was validated in the concentration range 0.025–10 mg L−1, while for ketorolac enantiomers in the concentration range 0.025–5 mg L−1. The lower limit of quantification was two times lower than in earlier described methods. The developed method was suitable for direct quantification of racemic ketorolac, p-hydroxy-ketorolac and ketorolac enantiomers in plasma and urine samples in women at delivery and in postpartum, enabling us to document significant intra-individual differences in pharmacokinetics between these physiological states.

  相似文献   
408.
In this study, we optimized method for the isolation and detection of lactoferrin from human saliva using 3 mm short monolithic disc. We optimized the conditions for separation as flow rate 4 mL min?1 and ionic strength of effluent as 2 M·NaCl. We estimated limit of detection of whole method, which was hyphenated to the Bradford’s assay, down to 100 ng mL?1. The purity of the isolated fractions was verified by sodium dodecyl sulphate-polyacrylamide gel electrophoresis and recovery of isolation was found to be 51 % using minimally processed sample of saliva. Further, we tested the optimized method on group of healthy volunteers (n = 7). We were able to distinguish between the healthy subjects and subject suffering from celiac disease, which reported at least 2.5× higher level of lactoferrin in comparison to healthy ones. The results were correlated with standard enzyme-linked immunosorbent assay (ELISA) kit with obtained correlation coefficient R 2 = 0.8446. Analysis of lactoferrin in saliva by monolithic disc and subsequent offline photometric detection is faster and cheaper method compared to ELISA commercial kit. The total analysis of one sample takes <20 min.  相似文献   
409.
We present a multi-species mole fraction and temperature sensor for in situ exhaust gas diagnostic of internal combustion (IC) engines. The sensor is based on Tunable Diode Laser Absorption Spectroscopy (TDLAS) and incorporates four optical channels - two miniature White cells and two double-traversal cells - with base lengths of 6?cm. It has been demonstrated at a hot air test stand and in the exhaust manifold of a single-cylinder research engine, with measured temperatures of up to 1000?K. Stable operation was achieved with absorption lengths of up to 192?cm (test stand) and 97?cm (engine). Employing time-division multiplexed detection, six species were measured simultaneously in the engine exhaust, at wavelengths ranging from 1.4?µm to 5.2 µm: water vapor (H2O), carbon dioxide (CO2), carbon monoxide (CO), methane (CH4), nitrogen dioxide (NO2) and nitric oxide (NO). The effective measurement rate was as high as 1?kHz, and cycle-to-cycle variations were clearly detected. We show the correlation of the air-fuel equivalence ratio with the spectroscopically measured mole fraction of each species. At a cycle-resolved rate, detection limits for the legally regulated species NO and NO2 were 1?ppm and 4?ppm, respectively. The sensor is intended to help improve the understanding of IC engine emission behavior during fast transients.  相似文献   
410.
Carbenes are very important reactive intermediates to access a variety of complex molecules and are applied widely in organic synthesis and drug discovery. Typically, their chemistry is accessed by the use of transition metal catalysts. Herein, we describe the application of low‐energy blue light for the photochemical generation of carbenes from donor–acceptor diazoalkanes. This catalyst‐free and operationally simple approach enables highly efficient cyclopropenation reactions with alkynes and the rearrangement of sulfides under mild reaction conditions, which can be utilized for both batch and continuous‐flow processes.  相似文献   
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