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11.
Liquefaction of gases offers deeper insight into the properties of various substances that are gaseous under normal conditions; however, the boiling temperatures of a number of gases are very low, preventing their liquefaction by means of standard laboratory techniques. A simple gas-liquefaction cell (designed by the authors) that can operate down to liquid-nitrogen temperature (77 K) is described in this paper. The properties of several liquefied (condensed) gases (e.g., ammonia, chlorine, nitric oxide, oxygen, and ozonized oxygen) are studied using this cell. The cell is also suitable for demonstration experiments.  相似文献   
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The structure of the sodiated peptide GGGGGGGG-Na+ or G8-Na+ was investigated by infrared multiple photon dissociation (IRMPD) spectroscopy and a combination of theoretical methods. IRMPD was carried out in both the fingerprint and N—H/O—H stretching regions. Modeling used the polarizable force field AMOEBA in conjunction with the replica-exchange molecular dynamics (REMD) method, allowing an efficient exploration of the potential energy surface. Geometries and energetics were further refined at B3LYP-D and MP2 quantum chemical levels. The IRMPD spectra indicate that there is no free C-terminus OH and that several N—Hs are free of hydrogen bonding, while several others are bound, however not very strongly. The structure must then be either of the charge solvation (CS) type with a hydrogen-bound acidic OH, or a salt bridge (SB). Extensive REMD searches generated several low-energy structures of both types. The most stable structures of each type are computed to be very close in energy. The computed energy barrier separating these structures is small enough that G8-Na+ is likely fluxional with easy proton transfer between the two peptide termini. There is, however, good agreement between experiment and computations in the entire spectral range for the CS isomer only, which thus appears to be the most likely structure of G8-Na+ at room temperature.  相似文献   
14.
In this note we are concerned with numerical solutions to Dirichlet problem $$[\phi(u')]' =f(x) \quad \mbox{in} [\alpha, \beta]; \quad u(\alpha)=A, \; u(\beta)=B, $$ where \(\phi :(-\eta , \eta ) \to \mathbb {R}\) \((\eta <+ \infty )\) is an increasing diffeomorphism with \(\phi '(y)\geq d >0\) for all \(y\in (-\eta , \eta )\) . The obtained algorithm combines the shooting method with Euler’s method and it is convergent whenever the problem is solvable. We provide numerical experiments confirming the theoretical aspects.  相似文献   
15.
The thermal stability of two kinds of dextran-coated magnetite (dextran with molecular weight of 40,000 (Dex40) and 70,000 (Dex70)), obtained by dextran adsorption onto the magnetite surface is investigated in comparison with free dextran in air and argon atmosphere. The thermal behavior of the two free dextran types and corresponding coated magnetites is similar, but atmosphere dependent. The magnetite catalyzes the thermal decomposition of dextran, the adsorbed dextran displaying lower initial decomposition temperatures comparative with the free one in both working atmospheres. The dextran adsorbed onto the magnetite surface decomposes in air through a strong sharp exothermic process up to ~450 °C while in argon atmosphere two endothermic stages are identified, one in the temperature range 160–450 °C and the other at 530–800 °C.  相似文献   
16.
In this study, different commercially available TiO2 powders (Degussa P25, pure anatase, and rutile) were submitted to selective dissolution treatments, with H2O2/NH4OH and 10% HF, known to remove rutile and anatase from physical mixtures. The aim was to check whether a particular separation method designed to remove a specific crystalline phase influences the properties of the other phase from the mixture or not. More precisely, we have studied how the HF dissolution method designed to selectively remove the anatase affected the physicochemical and photocatalytic properties of rutile. In a similar way, the changes in the anatase properties were studied, after the H2O2/NH4OH treatment, initially used to remove rutile from the mixture. All the samples were characterized by X-ray diffraction, nitrogen adsorption–desorption, transmission electron microscopy, diffuse reflectance (DR) ultraviolet–visible, and Raman spectroscopy. The photocatalytic activity of these powders was tested in the oxidation of p-chlorophenol from water. The selective treatment methods not only dissolved the target phase but also changed some physicochemical and the photocatalytic performances of the other TiO2 crystalline phase in a considerable manner. These aspects should be taken into account in the studies regarding the synergistic effects of anatase and rutile, especially in reconstructed TiO2 photocatalysts.  相似文献   
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This paper reports the effect of transfer line (TL) internal diameter (i.d.) on gas chromatographic separation characteristics such as efficiency and speed, when a multicapillary (MC) column is used for speciation analysis of mercury. Five different TL consisting of fused-silica capillaries with 0.15, 0.20, 0.25, 0.32, and 0.53 mm i.d. are compared. The separation efficiency and total chromatographic run time are critically affected by the i.d. of the TL. Narrow capillaries (i.d.0.20 mm) produce minimum peak dispersion whereas wide capillaries result in narrow peaks and shorter chromatographic analysis times. A thermodynamic approach is proposed to describe the motion of the analytes through the separation column and TL. The model provides good agreement with the experimental data for high pressures (35 psig) and wide TL (0.25 mm i.d.).Dedicated to the memory of Wilhelm Fresenius  相似文献   
18.
In this paper we study the existence and multiplicity of periodic solutions of pendulum-like perturbations of bounded or singular f{\phi}-Laplacians. Our approach relies on the Leray-Schauder degree and the upper and lower solutions method.  相似文献   
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Vibrational Sum Frequency Spectroscopy (VSFS) was employed to study adsorbing films of 4-Nitro Benzo-15-Crown-5 (NB15C5) and Benzo-15-Crown-5 (B15C5) at the aqueous solution-air interface. The surface of the solution is strongly influenced by the presence of crown ether species. Changes in the orientation of NB15C5 were monitored as a function of solution concentration, by targeting the ratio of peak intensities of the CN and NO(2) vibrational modes. The water of hydration has also been probed as a function of crown concentration, salt concentration, and temperature. The latter study strongly suggests that the surface can be treated as a charged interface, and that the associated ordered water decreases with increasing ionic strength of the bulk solution.  相似文献   
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