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91.
The effects of electron beam irradiation doses on the poly-tetra-fluoroethylene (PTFE) have been studied. Several techniques, such as X-ray diffraction (XRD), differential scanning calorimetry (DSC), mechanical properties and Fourier transform infrared spectroscopy (FTIR) were applied to characterize the PTFE samples and to study the radiation effects on the crystal structure of the polymer.The irradiation dose up to 150 kGy showed an increase in the crystallinity degree of PTFE, which has been observed and confirmed during the DSC and XRD measurements. The increase in crystallinity was attributed to the scissions of the chain in the amorphous region. Moreover, the number-average molecular weights were estimated from the heat of crystallization measured by DSC technique. The results indicated that the molecular weights were decreased by increasing the heat of crystallization due to irradiation with doses up to 150 kGy. Radiation resistance of the irradiated and non-irradiated PTFE was investigated during its mechanical properties at room temperature. The dose at half value of the elongation at break is about 3.10 kGy while the dose at half value of the tensile strength is about 1.70 kGy. 相似文献
92.
Allen W. Burton Stacey I. Zones Saleh Elomari 《Current Opinion in Colloid & Interface Science》2005,10(5-6):211-219
In this review we discuss the roles that inorganic and organic components play in the synthesis of high-silica zeolites. We discuss the effects that heteroatom identity, heteroatom substitution, and SDA shape have on synthesis products. Then we summarize recent developments in zeolite synthesis that have been made by performing syntheses in concentrated fluoride media and by using germanium as a tetravalent heteroatom. Finally, we examine the combined roles that framework stability, framework/SDA interactions, and silanol defects may have in determining phase selectivity. 相似文献
93.
94.
Speckle noise arises in imaging systems that use coherent or partially coherent illumination. We demonstrate that such noise may be reduced by use of bayesian filters. The usual assumption that speckle noise is approximately equivalent to multiplicative image noise is replaced with an exact analysis. 相似文献
95.
P.R. Elliston F. Habbal N. Saleh G.E. Watson K.W. Blazey H. Rohrer 《Journal of Physics and Chemistry of Solids》1975,36(9):877-881
Magnetic and optical measurements in the layer compound NaCrO2 are reported. This compound is antiferromagnetic with Tn = 46±2 K and θ = ?400±30 K. Broad antiferromagnetic resonances are observed which cannot be interpreted on any simple model. Optical absorption data are consistent with the appearance of antiferromagnetism. Non-intrinsic fluorescence has also been observed. 相似文献
96.
The role played by optical interference in determining the propagation of pulses in multimode fibers is examined under conditions of mode independence and mode coupling. Single pulses and pulse-pairs generated by a source that has arbitrary temporal and spatial coherence are considered, and the role played by the spatial integration at the detector, which effectively is a form of spatial incoherence, is investigated. It is shown that three forms of optical interference may result under different conditions of source spatiotemporal coherence—intramodal, intermodal, and interpulse interference. These effects change the profile of received pulses in a, in general, nonlinear way. 相似文献
97.
R.M. Saleh J.M. Abd El Kader A.A. El Hosary A.M. Shams El Din 《Journal of Electroanalytical Chemistry》1975,62(1):297-310
The dissolution of Cu in solutions of HNO3 of different concentrations has been studied by the thermometric method. Starting from the initial temperature, Ti, the temperature—time curves exhibit an induction period followed by a rapid rise in temperature to a maximum value, Tm, attained t min after the start of the reaction. Tm increases and t decreases with increase of the acid concentration, M. ΔT (i.e.Tm ? Ti) and the reaction number (R.N. = (Tm ? Ti)/t) vary with M according to: ΔT = k(M ? M0) and R.N. = A1Mn, where k, M0, A1 and n are constants.The effect of varying concentrations of HCl, H2SO4 and H3PO4 on the R.N. of Cu in 3.5 M HNO3 was examined. Small amounts of these acids lower the R.N. (inhibition) due to the displacement of an active species on the surface of the metal by the anion of the acid. Larger additions of the acids accelerate dissolution. The concentration at which the added acid changes from corrosion-inhibitor to accelerator varies as HCl < H2SO4 < H3PO4. This sequence is considered to parallel the strength of adsorption of the respective anions. The results of experiments with salt additions confirm this view; all salts act only as dissolution-retardants. Calculations pertaining to the effect of the various ions on the R.N. support the conclusion that the dissolution of Cu in HNO3 is autocatalytic in nature, and depends on the [H+]/[NO3?] ratio.Cu does not dissolve in air-free, cold HCl. Attack takes place, however, in the presence of KNO3. Under these conditions attack is of the pitting- rather than the general type. The temperature rises suddenly after an incubation period, which decreases in length with increase of the amount of the added salt.Proof of the involvement of HNO2 in the autocatalytic cycle of Cu dissolution in HNO3 is obtained from the results of urea additions to the solution. 相似文献
98.
An electrochemical detector cell having a dropping-mercury working electrode and an Ag/ AgCl reference electrode is examined with reference to applications in flow-injection analysis and high-performance liquid chromatography. The working electrode, fed by a horizontal capillary, is capable of delivering mercury at fast dropping rates which can be varied by a control device in the cell. Examples of application to inorganic and organic electroreducible species are considered and advantages and limitations relative to other electrochemical detector devices are discussed. 相似文献
99.
Nuclear gamma resonance spectroscopy, also known as M?ssbauer spectroscopy, is a technique that probes transitions between the nuclear ground state and a low-lying nuclear excited state. The nucleus most amenable to M?ssbauer spectroscopy is 57Fe, and 57Fe M?ssbauer spectroscopy provides detailed information about the chemical environment and electronic structure of iron. Iron is by far the most structurally and functionally diverse metal ion in biology, and 57Fe M?ssbauer spectroscopy has played an important role in the elucidation of its biochemistry. In this article, we give a brief introduction to the technique and then focus on two recent exciting developments pertaining to the application of 57Fe M?ssbauer spectroscopy in biochemistry. The first is the use of the rapid freeze-quench method in conjunction with M?ssbauer spectroscopy to monitor changes at the Fe site during a biochemical reaction. This method has allowed for trapping and subsequent detailed spectroscopic characterization of reactive intermediates and thus has provided unique insight into the reaction mechanisms of Fe-containing enzymes. We outline the methodology using two examples: (1) oxygen activation by the non-heme diiron enzymes and (2) oxygen activation by taurine:alpha-ketoglutarate dioxygenase (TauD). The second development concerns the calculation of M?ssbauer parameters using density functional theory (DFT) methods. By using the example of TauD, we show that comparison of experimental M?ssbauer parameters with those obtained from calculations on model systems can be used to provide insight into the structure of a reaction intermediate. 相似文献
100.