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1.
Mathematical Programming - In this paper we study the convergence of an Inertial Forward–Backward algorithm, with a particular choice of an over-relaxation term. In particular we show that...  相似文献   
2.
Cardiovascular diseases (CVDs) have been associated with environmental pollutants. The scope of this study is to assess any potential relation of polycyclic aromatic hydrocarbons (PAHs), their hydroxylated derivatives, and trace elements with heart failure via their direct determination in human serum of Greek citizens residing in different areas. Therefore, we analyzed 131 samples including cases (heart failure patients) and controls (healthy donors), and the respective demographic data were collected. Significantly higher concentrations (p < 0.05) were observed in cases’ serum regarding most of the examined PAHs and their derivatives with phenanthrene, fluorene, and fluoranthene being the most abundant (median of >50 μg L−1). Among the examined trace elements, As, Cd, Cu, Hg, Ni, and Pb were measured at statistically higher concentrations (p < 0.05) in cases’ samples, with only Cr being significantly higher in controls. The potential impact of environmental factors such as smoking and area of residence has been evaluated. Specific PAHs and trace elements could be possibly related with heart failure development. Atmospheric degradation and smoking habit appeared to have a significant impact on the analytes’ serum concentrations. PCA–logistic regression analysis could possibly reveal common mechanisms among the analytes enhancing the hypothesis that they may pose a significant risk for CVD development.  相似文献   
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The effects of rice (Oryza sativa L.) cultivation under flooded conditions on soil’s physical-hydraulic properties were studied in this article, using a new methodology based on a combined analysis on soil water retention curve (WRC) and pore size distribution (PSD). WRC analysis was carried out through the changes of van Genuchten’s model parameters, the characteristics of WRC at the inflection point, and the specific water capacity curve. Analysis of PSD was performed on the volume changes of porosity fractions through a detailed pore size classification, while different pore size classifications based on their hydraulic and structural characteristics were also used. The methodology was applied using a small dataset obtained from fine-textured Entisol soils which were subjected to rice cultivation under flooded conditions in Axios River plain (Northern Greece). Measurements of WRC were obtained at four depths of the soil profile from two fields, before and after the growing season of rice. The analysis indicated that the van Genuchten’s model parameters (θ s, a, and n) and the WRC characteristics at the inflection point (pressure head h i , pore equivalent diameter D i , and slope S i ) significantly changed after the growing season following similar patterns, along the soil profile in both fields. The parameters θ s, a, D i , and S i were decreased, while n and h i were increased. The h i and a were the most sensitive parameters, while the values of (h i and 1/a) in each layer before and after the growing season for each field were linearly correlated and shifted to higher values because of compaction, indicating that it could be applied as a tool to evaluate the degree of soil compaction to similarly textured soils. The peaks of the specific water capacity curves were compressed (lower values of slope S i ) and shifted to lower water potentials (h i ) that corresponded to pores of equivalent diameter D i between 2 and 6 μm. The soils had few structural pores (>9 μm) and low air-filled porosity (>30 μm) before the growing season, which presented accessory reduction after the growing season in both fields. Total porosity was reduced at the expense of structural porosity along the soil profile, while the pore size class of 5–3 μm was identified as the threshold where the smaller pores’ volume started to increase in all layers of both fields. The results indicated that the changes in the WRC and the PSD follow specific trends, which can be used in future studies to model temporal variability of soil’s physical-hydraulic properties.  相似文献   
5.
It is proved that every subspace of James Tree space (JT) with non-separable dual contains an isomorph of James Tree complemented in JT. This yields that every complemented subspace of JT with non-separable dual is isomorphic to JT. A new JT like space denoted as TF is defined. It is shown that every subspace of James Function space (JF) with non-separable dual contains an isomorph of TF. The later yields that every subspace of JF with non-separable dual contains isomorphs of c0 and ?p for 2?p<∞. The analogues of the above results for bounded linear operators are also proved.  相似文献   
6.
The reaction of Zn(acac)2 with btaH (1,2,3-benzotriazole) in dmf yielded the pentanuclear complex [Zn5(bta)6(acac)4(dmf)]·dmf (1·dmf). In the presence of pyrazine, the pentanuclear [Zn5(bta)6(acac)4(dmf)]·3.7dmf (2·3.7dmf) and enneanuclear [Zn9(bta)12(acac)6]·6dmf (3·6dmf) complexes were formed, whereas in the presence of 4,4′-bpy the 1D coordination polymer [Zn(acac)2(4,4′-bpy)]n (4) was isolated. The molecular structures of 1·dmf and 2·3.7dmf reveal that the [Zn5] clusters consist of four ZnII ions which span the corners of a tetrahedron and the fifth resides at its centre. The molecular structure of 3·6dmf reveals that the [Zn9] clusters consist of two corner sharing tetrahedra and the structure can be described as the addition of two [Zn5] clusters of 1·dmf and/or 2·3.7dmf followed by the simultaneous abstraction of [Zn(acac)2] and dmf molecules; this alternative was accomplished by recrystallization of 1·dmf from dmf which yielded 3·6dmf. Each of the μ3N:κN′:κN′′ benzotriazolate ligands in 1·dmf, 2·3.7dmf and 3·6dmf spans an edge of the tetrahedron. The molecular structure of 4 reveals mononuclear [Zn(acac)2] units bridged via 4,4′-bpy molecules to 1D coordination polymer. Characteristic IR bands of the four complexes are discussed in terms of the coordination modes of the ligands and known structures.  相似文献   
7.
The use of salicylaldehyde oxime (H2salox) in manganese(III) carboxylate chemistry has yielded new members of the family of hexanuclear compounds presenting the [Mn63-O)22-OR)2]12+ core, complexes [MnIII63-O)2(O2CPh)2(salox)6(L1)2(L2)2] (L1 = py, L2 = H2O (1); L1 = Me2CO, L2 = H2O (2); L1 = L2 = MeOH (3)). Addition of NaOMe to the acetonitrile reaction mixture, afforded the 1D complex [MnIII3Na(μ3-O)(O2CPh)2(salox)3(MeCN)]n (4), whereas addition of NaClO4 to the acetone reaction mixture afforded an analogous 1D complex [MnIII3Na(μ3-O)(O2CPh)2(salox)3(Me2CO)]n (5). The structures of 1–3 present the [Mn63-O)22-OR)2]12+ core and can be described as two [Mn33-O)]7+ triangular subunits linked by two μ2-oximato oxygen atoms of the salox2− ligands, which show the less common μ32OO′:κN coordination mode. The benzoato ligands are coordinated through the usual syn,syn2OO′ mode. The 1D polymeric structures of 4 and 5 consist of alternating [Mn33-O)]7+ subunits and Na+ atoms linked through two μ32OO′:κN and one μ42O2O′:κN salox2− ligands as well as one syn,anti2OO′ benzoato ligand. DC and AC magnetic susceptibility studies on 1 revealed the stabilization of an S = 4 ground state, and indications of single-molecule magnetism behavior, whereas the DC experimental data from polycrystalline sample of 5 are indicative of antiferromagnetic interactions within the [Mn3] subunit. Solid state 1H NMR data of 1 were used to probe the spin-lattice relaxation of the system.  相似文献   
8.
It is an observational fact that density waves in vehicle traffic can move in either direction: small-amplitude waves travel in the same direction as the cars (downstream) whereas high-amplitude waves or “jams” travel in the opposite direction (upstream). We construct a model of ring road traffic to demonstrate how this comes about. Our model shows the spontaneous generation of these density waves, explains their stability properties, and pinpoints the precise density level at which the wave speed changes direction.  相似文献   
9.
An analytical method for the determination of both sulfadiazine (SDZ) and trimethoprim (TMP), and also N4-acetyl-sulfadiazine (AcSDZ), the main metabolite of SDZ, in fish muscle plus skin has been developed and validated. Dapsone was used as internal standard. The method involves extraction of the analytes from fish tissue by pressurized liquid extraction using water as extractant. Sample cleanup was carried out by solid phase extraction using Abselut Nexus cartridges. Target analytes were quantitatively determined by liquid–chromatography mass spectrometry using single ion monitoring. The developed method was validated according to the European Union requirements (decision 2002/657/EC). The limit of detection for SDZ and AcSDZ was 3.0 and 2.5 µg kg?1 for TMP. The limit of quantification (LOQ) was 10 µg kg?1 for SDZ and AcSDZ and 7.5 µg kg?1 for TMP. The recovery experiments carried out included the concentration levels of 0.5, 1 and 1.5 times the MRLs for SDZ and TMP. Concentration levels for AcSDZ were the same as SDZ. The values obtained were higher than 92.0% with coefficient of variation (CV, %) below 8.6%. The precision of the method, calculated as CV (%), ranged from 0.2 to 6.8% and from 0.8 to 8.9% for intra–day and inter–day analysis, respectively. Decision limit (CCα) was calculated as 104.3, 53.7 and 105.3 µg kg?1 for SDZ, TMP and AcSDZ, respectively. Detection capability (CCβ) was calculated as 110.0, 58.8 and 109.7 µg kg?1 for SDZ, TMP and AcSDZ, respectively. “Matrix effect” and “relative matrix effect” were also evaluated. The method was used for the analysis of fish samples purchased from local markets.  相似文献   
10.
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