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141.
The authors describe an amperometric biosensor for the determination As(III) and Cd(II) based on the inhibition of the enzyme acetylcholineesterase (AChE). A platinum electrode was modified with ruthenium(II)-tris(bipyridyl), graphene oxide and AChE and then showed redox peaks at 0.06 and 0.2 V vs Ag/AgCl in the presence of acetylthiocholine chloride (ATChCl). Amperometry unveiled a steady-state turnover rate with the release of thiocholine. In the presence of arsenic(III) and cadmium(II), AChE showed an inhibitive response at 0.214 and 0.233 V vs Ag/AgCl, respectively. The electrode exhibits a detection limit and linear range of 0.03 μM and 0.05–0.8 μM for As(III) and 0.07 μM and 0.02–0.7 μM for Cd(II), respectively. Type of inhibition and inhibition constants induced by As(III) and Cd(II) on the catalytic sites of AChE were determined from Dixon and Lineweaver-Burk plots. The modified electrode was applied to the determination of As3+ and Cd2+ in river, tap and waste water, and the results proved that the method is sensitive and can be an alternative to chromatographic and spectroscopic techniques.
Graphical abstract Schematic presentation of Pt/Ru(II)-tris(bipy)-GO/AChE electrode in absence and presence of metal ions (As3+/Cd2+).
  相似文献   
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143.
A new application of Staudinger’s phosphazene as an efficient esterifying reagent is reported. Staudinger’s phosphazene formed in situ by the reaction of organic mono-azide with triphenylphosphine, which is trapped by carboxylic acid, to afford amide exclusively. In contrast, interestingly the same phosphazene behaves in a different way as an efficient esterifying reagent, affording ester under a solvent-free microwave-assisted protocol wherein alcohol is added as the another component in addition to the other reactants. This discovery adds yet another new application of Staudinger’s phosphazene to synthetic chemistry.  相似文献   
144.
A novel series of four-ring achiral ferroelectric liquid crystals containing 1,2,4-oxadiazole cores with unsymmetrical substitutions at C-3 and C-5 positions are synthesised and characterised. A fluoro substituted biphenyl moiety is prepared by Suzuki coupling reaction and is directly attached to the oxadiazole core at the C-5 position for the first time in the literature. An octyl benzoate is attached to the oxadiazole core at the C-3 position of it. All the compounds exhibit polar smectic (B2) mesophases with ferroelectric switching along with the orthogonal smectic-A mesophases. These compounds possess high mesomorphic thermal ranges of polar smectic phases and are towards the ambient temperatures. The influence of a more electronegative fluorine substituent on the electron rich biphenyl moiety (at the C-5 position) of the oxadiazole core is analysed for the prevalence and abundance of polar smectic (ferroelectric) mesophases.  相似文献   
145.
The authors report on the fabrication of Co(OH)2-enfolded Cu2O nanocubes on reduced graphene oxide (rGO), and the use of this material in an electrochemical caffeine sensor. The rGO/Cu2O/Co(OH)2 composite was characterized by X-ray powder diffraction pattern analysis, field emission scanning electron microscopy, energy dispersive X-ray spectroscopy and Raman spectroscopy. A rotating disc glassy carbon electrode covered with the nanocomposite displays enhanced electrocatalytic activity towards the electro-oxidation of caffeine. The peak oxidation potential is at 1.4  V (vs. Ag/AgCl) and hence is strongly shifted to the negative side when compared to other modified electrodes. The calibration plot is linear in the 0.83 to 1200 μM concentration range, with a 0.4 μM detection limit (at a signal-to-noise ratio of 3). The modified electrode is sensitive, selective and stable. It was successfully applied to the determination of caffeine in (spiked) caffeine-containing beverages and coffee powder and gave recoveries that ranged from 95.7 to 98.3 %.
Graphical abstract Co(OH)2 enfolded Cu2O nanocubes on reduced graphene oxide (rGO) for the caffeine sensor
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The impact of green-synthesised mosquitocidal nanoparticles on non-target aquatic predators is poorly studied. In this research, we proposed a single-step method to synthesise silver nanoparticles (Ag NP) using the seed extract of Melia azedarach. Ag NP were characterised using a variety of biophysical methods, including UV–vis spectrophotometry, scanning electron microscopy, energy-dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. In laboratory assays on Anopheles stephensi, Ag NP showed LC50 ranging from 2.897 (I instar larvae) to 14.548 ppm (pupae). In the field, the application of Ag NP (10 × LC50) lead to complete elimination of larval populations after 72 h. The application of Ag NP in the aquatic environment did not show negative adverse effects on predatory efficiency of the mosquito natural enemy Cyclops vernalis. Overall, this study highlights the concrete possibility to employ M. azedarach-synthesised Ag NP on young instars of malaria vectors.  相似文献   
148.
In this work, dehydration of sodium diphosphate decahydrate Na4P2O7⋅10H2O and phase transformations of Na4P2O7 in open air have been studied in detail by thermo-Raman spectroscopy. The spectra were measured continuously in a temperature range from room temperature up to 600°C for the bands of P2O7 4- and H2O. The spectral variation showed one step of dehydration and four-phase transformations. The thermo-Raman intensity(TRI) and differential thermo-Raman intensity (DTRI) curves calculated from the characteristic bands of H2O also showed one step of dehydration with the loss of all hydrated water in the temperature interval from 45 to 69°C. Thermogravimetric measurements supported this result. The thermo-Raman investigation indicated the transformation of Na4P2O7 from low temperature phase to high temperature phase proceed through pre-transitional region from 75 to 410°C before the major orientational disorder at 418°C and minor structural modifications at 511,540 and 560°C. The results from differential scanning calorimetry and differential thermal analysis on Na4P2O7 showed endotherms at 407,517, 523, 548, 557°C and 426, 528, 534, 555, 565°C, respectively. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   
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150.
Multilevel Hadamard matrices (MHMs), whose entries are integers as opposed to the traditional restriction to {±1}, were introduced by Trinh, Fan, and Gabidulin in 2006 as a way to construct multilevel zero-correlation zone sequences, which have been studied for use in approximately synchronized code division multiple access systems. We answer the open question concerning the maximum number of distinct elements permissible in an order n MHM by proving the existence of an order n MHM with n elements of distinct absolute value for all n. We also define multidimensional MHMs and prove an analogous existence result.   相似文献   
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