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The existence of coincidence points and common fixed points for mappings satisfying certain contractive conditions, without appealing to continuity, in a cone metric space is established. These results generalize several well-known comparable results in the literature.  相似文献   
134.
Structural health monitoring (SHM) is recognized as an efficient tool to interpret the reliability of a wide variety of infrastructures. To identify the structural abnormality by utilizing the electromechanical coupling property of piezoelectric transducers, the electromechanical impedance (EMI) approach is preferred. However, in real-time SHM applications, the monitored structure is exposed to several varying environmental and operating conditions (EOCs). The previous study has recognized the temperature variations as one of the serious EOCs that affect the optimal performance of the damage inspection process. In this framework, an experimental setup is developed in current research to identify the presence of fatigue crack in stainless steel (304) beam using EMI approach and estimate the effect of temperature variations on the electrical impedance of the piezoelectric sensors. A regular series of experiments are executed in a controlled temperature environment (25°C–160°C) using 202 V1 Constant Temperature Drying Oven Chamber (Q/TBXR20-2005). It has been observed that the dielectric constant ε33T which is recognized as the temperature-dependent constant of PZT sensor has sufficiently influenced the electrical impedance signature. Moreover, the effective frequency shift (EFS) approach is optimized in term of significant temperature compensation for the current impedance signature of PZT sensor relative to the reference signature at the extended frequency bandwidth of the developed measurement system with better outcomes as compared to the previous literature work. Hence, the current study also deals efficiently with the critical issue of the width of the frequency band for temperature compensation based on the frequency shift in SHM. The results of the experimental study demonstrate that the proposed methodology is qualified for the damage inspection in real-time monitoring applications under the temperature variations. It is capable to exclude one of the major reasons of false fault diagnosis by compensating the consequence of elevated temperature at extended frequency bandwidth in SHM.  相似文献   
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Molecular Diversity - Soluble epoxide hydrolase (sEH) enzyme plays an important role in the metabolism of endogenous chemical mediators, epoxyeicosatrienoic acids, which are involved in the...  相似文献   
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Bimetallic chlorodi-/triorganotin(IV) derivatives of general formulas R2(H2O)SnLCSSSn(Cl)R2 (R=Me: 1; Ph: 2) and R3Sn(Na)LCSSSnR3·H2O (R=Bu: 3; Ph: 4) were prepared by reaction of iminodiacetic acid disodium salt hydrate (Na2LH) with CS2 and R2SnCl2/R3SnCl in methanol. The reaction between Na2LH, CS2, and PdCl2 produced [Na2LCSS]2Pd·2H2O (5) which was treated with R3SnCl to synthesize the heterobimetallic derivatives [R3Sn(Na)LCSS]2Pd·2H2O (R=Me: 6; Ph: 7). The complexes were characterized by microanalysis, spectroscopic, and thermogravimetric analyses. Elemental analysis data, mass fragmentation, and thermal degradation patterns supported the molecular composition of the complexes. FT-IR data indicated monodentate binding of carboxylate while a chelating coordination mode of the dithiocarboxylate was verified in the solid state. A five-coordinate tin(IV) was demonstrated in the solid state. In solution, a tetrahedral/trigonal bipyramidal configuration around Sn(IV) and a square planar geometry of Pd(II) was indicated by multinuclear NMR (1H and 13C) and UV-visible studies. The Pd(II) derivatives showed interaction with salmon sperm-DNA and caused an inhibition of alkaline phosphatase (ALPs). The antibacterial/antifungal potential of the coordination products varied with the nature of incorporated metal and a substitution pattern at tin(IV); the palladium metallation decreased the antimicrobial activities. The triorganotin(IV) products exhibited more powerful action against bacteria/fungi as compared to their diorganotin(IV) counterparts. The complexes displayed sufficiently lower hemolytic effects in vitro as compared to triton X-100 and slightly higher than PBS.  相似文献   
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通过可控的水热生长方法和钴铁碳酸根氢氧根水合物的焙烧在泡沫铁上制备了CoFe2O4纳米阵列催化剂。通过粉末X射线衍射,扫描电镜和电感耦合等离子体发射光谱表征了CoFe2O4纳米阵列的晶相,结构和组成。制备的催化剂被用于费托合成性能研究。CoFe2O4纳米阵列催化剂在5L/(g·h)的空速下具有69%的转化率,并且其性能优于粉体催化剂。  相似文献   
139.
A novel and sensitive extraction procedure using maghemite nanoparticles (γ-Fe2O3) modified with sodium dodecyl sulfate (SDS), as an efficient solid phase, was developed for removal, preconcentration and spectrophotometric determination of trace amounts of malachite green (MG) and leuco-malachite green (LMG). Combination of nanoparticle adsorption and easily magnetic separation was used to extraction and desorption of MG and LMG. The adsorption capacity was evaluated using both the Langmuir and Freundlich adsorption isotherm models. Maghemite nanoparticles were prepared by co-precipitation method and their surfaces were modified by SDS. The size and properties of the produced maghemite nanoparticles was determined by X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM) and BET analysis. MG and LMG became adsorbed at pH 3.0. LMG was oxidized to MG by adsorption on maghemite nanoparticles. The adsorbed MG was then desorbed and determined spectrophotometrically. The calibration graph was linear in the range 0.50-250.00 ng mL−1 of MG and LMG with a correlation coefficient of 0.9991. The detection limit of the method for determination of MG was 0.28 ng mL−1 and the relative standard deviation (R.S.D.) for 10.00 and 50.00 ng mL−1 of malachite green was 1.60% (n = 3) and 0.86% (= 5), respectively. A preconcentration factor of 50 was achieved in this method. The Langmuir adsorption capacity (qmax) was found to be 227.3 mg g−1 of the adsorbent. The method was applied to the determination of MG in fish farming water samples.  相似文献   
140.
A novel, simple and sensitive adsorptive stripping voltammetry method was developed for simultaneous determination of Cd and Zn using N‐Nitrozo‐N‐phenylhydroxylamine (Cupferron) as a selective complexing agent. Cadmium and zinc metals gave peaks that were distinctly separated by 450–1200 mV, allowing their determination over a wide range of concentrations. The influence of pH and the nature of supporting electrolytes, concentration of ligand, preconcentration time and applied potential were investigated. The detection limits were 0.058 ng/mL for Zn and 0.092 ng/mL for Cd, and the RSD at a concentration level of 50 ppb, were 1.8–2.1 % for both zinc and cadmium, respectively. The method was applied to the determination of cadmium and zinc in blood, drug, food and water samples with the satisfactory results.  相似文献   
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