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1.
This study assesses whether the concentrations of biologically important elements in bones are altered by long‐term consumption of cadmium (Cd)‐contaminated water. Heavy metal poisoning has significant impact on humans, and pollutants such as Cd are often found at high concentrations in waterways. Twelve Sprague Dawley rats consumed water with 50 p.p.m. Cd (Cd group), and another 12 consumed normal water (control group). Six subjects from each group were sacrificed after 2 weeks and the others after 4 weeks. Spectra were acquired from the femur by using the EDAX Eagle III micro‐XRF setup, and quantitative calculations were performed by using the fundamental parameter method to determine the concentrations of elements. A bone calcium/phosphorus concentration ratio (Ca/P) of 2.07 ± 0.001 is observed in the spectra from control subjects after 2 weeks and 2.07 ± 0.001 after 4 weeks. In Cd subjects, Ca/P after 2 weeks is 2.04 ± 0.001 and after 4 weeks is 1.97 ± 0.003. Statistically significant differences are obtained when comparing controls with Cd subjects at both time points and when comparing Cd subjects at both time points. Cadmium poisoning significantly affects bone Ca and P concentrations, increasing the likelihood of osteoporosis and other bone diseases. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   
2.
Laminar flame speeds were accurately measured for CO/H2/air and CO/H2/O2/helium mixtures at different equivalence ratios and mixing ratios by the constant-pressure spherical flame technique for pressures up to 40 atmospheres. A kinetic mechanism based on recently published reaction rate constants is presented to model these measured laminar flame speeds as well as a limited set of other experimental data. The reaction rate constant of CO + HO2 → CO2 + OH was determined to be k = 1.15 × 105T2.278 exp(−17.55 kcal/RT) cm3 mol−1 s−1 at 300-2500 K by ab initio calculations. The kinetic model accurately predicts our measured flame speeds and the non-premixed counterflow ignition temperatures determined in our previous study, as well as homogeneous system data from literature, such as concentration profiles from flow reactor and ignition delay time from shock tube experiments.  相似文献   
3.
We do the tentative beginnings of a study of BLT-sets of generalised quadrangles via their symmetries. In particular, the study of whorls about a line leads us to hyperbolic reflections preserving a BLT-set of Q(4, q).  相似文献   
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Catalytic ignition and heat release of methane oxidation over a Pd wire covered with a 1–2 μm PdO surface layer were investigated by wire microcalorimetry over the temperature range of 600–770 K and pressure range of 0.5–4 atm. Ignition temperatures and heat release rates for different methane concentrations (1–4 vol.% in dry air) were determined, showing that the ignition temperatures decrease with increasing the methane concentration and increasing ambient pressure. At total pressure of 1 atm and 2% methane concentration, the global activation energy for the catalytic reaction is 21.5 ± 0.9 kcal/mol and 14.3 ± 0.2 kcal/mol in the temperature ranges of 600–670 K and 670–770 K, respectively. The reaction order for methane is 0.9 ± 0.1 over the temperature range of 630–770 K.  相似文献   
7.
The combustion characteristics of freely falling droplets, individually generated by the merging of colliding methanol and alkane droplets, were investigated and compared with those for pure methanol and alkanes. The merging of the nominally immiscible methanol and alkanes was manifested in an apparently adhesive, but unmixed, manner in all test conditions. An air bubble was found to be trapped at the colliding interfaces where they were “adhered,” with the trapping favored for head-on or near head-on collision orientations. The trapped air bubble ostensibly induced heterogeneous nucleation of the methanol, being facilitated by the relatively low limit of superheat of methanol. Consequently, the droplet exploded almost immediately upon ignition, leading to an extremely short overall lifetime. For collision orientations that were more off-centered, bubble trapping and thereby heterogeneous nucleation were not favored. However, delayed, albeit strong, microexplosion occurred through homogeneous nucleation of methanol at the contacting interface. The global burning rate was therefore again augmented. In general, microexplosion was facilitated for high-boiling-point alkanes such as hexadecane and tetradecane. The co-vaporization of methanol and alkane from their respective hemispherical segments constituting the adhered droplet also led to flame colors that were more bluish than yellowish, indicating the reduction of soot from alkane burning in the presence of methanol vapor. In light of the difficulty of forming stable methanol/oil emulsions, the potential of separate injection of oil and methanol in opposed jet arrangement, in direct-injection engines to facilitate collision, is suggested.  相似文献   
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Background  

The adenine nucleotide translocator 1 (Ant1) is an inner mitochondrial membrane protein involved with energy mobilization during oxidative phosphorylation. We recently showed that rodent Ant1 is upregulated by transforming growth factor-beta (TGF-β) in reactive astrocytes following CNS injury. In the present study, we describe the molecular mechanisms by which TGF-β1 regulates Ant1 gene expression in cultured primary rodent astrocytes.  相似文献   
9.
Successful demonstration of selective area doping of planar glass samples for monolithic integration of optically passive and active devices on a single chip is presented. Salt solution of erbium was delivered onto pre-sintered germano-silicate samples via a syringe. The samples were then consolidated to form dense glass layers containing regions doped with rare earth. Erbium tri-chloride solution, 0.1 M, was used during the solution doping phase, with the resulting erbium atomic percentage ranging from more than 0.1-0.4%, increasing linearly with the number of drips applied.  相似文献   
10.
A linear stability analysis is conducted to study the onset of near-limit flame oscillation with radiative heat loss in 1-D chambered planar flames using multi-scale activation-energy asymptotics. The oscillatory instability near the radiation-induced extinction limit at large Damköhler numbers is identified, in additional to the one near the kinetic limit at small Damköhler numbers. It is shown that radiative loss assumes a similar role as varying the thermal diffusivity of the reactants. Thus, flame oscillation near the radiative limit is still thermal-diffusive in nature although it may develop under unity Lewis numbers. The unstable range of Damköhler numbers near the radiative limit shows quite similar parametric dependence on the Lewis numbers of reactants, LeF and LeO, the stoichiometry, ?, and the radiative loss as that near the kinetic limit. They both increase monotonically with LeO and ? and increase then decrease with LeF. Increasing radiative loss extends the parameter range under which flame oscillations may develop. However, they show different dependence on the temperature difference between the supplying reactants. Unless radiative loss approaches its maximum value the system can sustain, flame oscillation near the radiative limit is only possible within a limited range of ΔT, whereas it is promoted monotonically with decreasing ΔT near the kinetic limit. Furthermore, while radiative loss shows small effect on the nondimensional oscillation frequency, the dimensional frequency of flame oscillations near the radiative limit can be substantially smaller than that near the kinetic limit.  相似文献   
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