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1.
Saxifraga atrata is an important traditional Tibetan medicine used to treat cough and pneumonia, and has tremendous medicinal potential. In this study, we devised a technique to separate 1,1-diphenyl-2-picrylhydrazyl inhibitors from a methanol extract of S. atrata. The material was first processed using MCI GEL CHP20P medium-pressure liquid chromatography, yielding 1.1 g of the target fraction Fr2. Subsequently, online hydrophilic interaction liquid chromatography-1,1-diphenyl-2-picrylhydrazyl assay was used to identify prospective 1,1-diphenyl-2-picrylhydrazyl inhibitors, and two 1,1-diphenyl-2-picrylhydrazyl inhibitor fractions (Fr24 and Fr25) were identified from Fr2. Then, medium-pressure preparation was continued using an XIon column to separate two 1,1-diphenyl-2-picrylhydrazyl inhibitor fractions (Fr24 and Fr25). The target compound was concentrated in fractions Fr24 and Fr25 using reverse-phase liquid chromatography during further separation procedures. Finally, the purity, structure, and 1,1-diphenyl-2-picrylhydrazyl inhibitory activity of the isolated 1,1-diphenyl-2-picrylhydrazyl inhibitors were determined. Two 1,1-diphenyl-2-picrylhydrazyl inhibitors (adenosine with the half maximal inhibitory concentration of 66.87 ± 14.33 μM and (-)-4-O-(E)-caffeoyl-l -threonic acid with the half maximal inhibitory concentration of 59.06 ± 5.02 μM) were isolated with purities exceeding 95%. The results showed that this technology is effective in the targeted separation of antioxidants from natural products.  相似文献   
2.
The chiral separation of various analytes (dichlorprop, mecoprop, ibuprofen, and ketoprofen) was demonstrated with different cyclodextrins as mobile phase additives in open-tubular liquid chromatography using a stationary pseudophase semipermanent coating. The stable coating was prepared by a successive multiple ionic layer approach using poly(diallyldimethylammonium chloride), polystyrene sulfonate, and didodecyldimethyl ammonium bromide. Increasing concentrations (0–0.2 mM) of various native and derivatized cyclodextrins in 25 mM sodium tetraborate (pH 9.2) were investigated. Chiral separation was achieved for the four test analytes using 0.05–0.1 mM β-cyclodextrin (resolution between 1.11 and 1.34), γ-cyclodextrin (resolution between 0.78 and 1.27), carboxymethyl-β-cyclodextrin (resolution between 1.64 and 2.59), and 2-hydroxypropyl-β-cyclodextrin (resolution between 0.71 and 1.76) with the highest resolutions obtained with 0.1 mM carboxymethyl-β-cyclodextrin. %RSD values were <10%. This is the first demonstration of chiral open-tubular liquid chromatography using achiral chromatographic coatings and cyclodextrins as mobile phase additives.  相似文献   
3.
Adsorptive separation of C2H6 from C2H4 by adsorbents is an energy-efficient and promising method to boost the polymer grades C2H4 production. However, that C2H6 and C2H4 display very similar physical properties, making their separation extremely challenging. In this work, by regulating the pore environment in a family of chitosan-based carbon materials (C-CTS-1, C-CTS-2, C-CTS-4, and C-CTS-6)- we target ultrahigh C2H6 uptake and C2H6/C2H4 separation, which exceeds most benchmark carbon materials. Explicitly, the C2H6 uptake of C-CTS-2 (166 cm3/g at 100 kPa and 298 K) has the second-highest adsorption capacity among all the porous materials. In addition, C-CTS-2 gives C2H6/C2H4 selectivity of 1.75 toward a 1:15 mixture of C2H6/C2H4. Notably, the adsorption enthalpies for C2H6 in C-CTS-2 are low (21.3 kJ/mol), which will facilitate regeneration in mild conditions. Furthermore, C2H6/C2H4 separation performance was confirmed by binary breakthrough experiments. Under different ethane/ethylene ratios, C-CTS-X extracts a low ethane concentration from an ethane/ethylene mixture and produces high-purity C2H4 in one step. Spectroscopic measurement and diffraction analysis provide critical insight into the adsorption/separation mechanism. The nitrogen functional groups on the surface play a vital role in improving C2H6/C2H4 selectivity, and the adsorption capacities depend on the pore size and micropore volume. Moreover, these robust porous materials exhibit outstanding stability (up to 800 °C) and can be easily prepared on a large scale (kg) at a low cost (~$26 per kg), which is very significant for potential industrial applications.  相似文献   
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We propose a novel device structure with a WO3/NiOx bilayer to improve the hole injection ability in QLEDs fabricated mainly by a solution-based process. First, we employed a spin-coated NiOx thin film as a hole injection layer (HIL) to replace Poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) PEDOT:PSS which corrodes indium tin oxide (ITO) used as an anode in QLEDs. We showed a simply optimized annealing process, instead of a rather complicated process like doping, can improve the electrical conductivity of the NiOx thin film. The reason for the dependency of conductivity on the post-metallization annealing is because of the change of the total amount of Ni vacancy in the NiOx thin film as a function of annealing temperature: The electrical conductivity of the NiOx thin film annealed at 275 °C was the best in this work. Second, we inserted the WO3 thin film in between ITO electrode and NiOx HIL to form an ITO/WO3/NiOx structure which reduces the hole injection barrier to 0.35 eV, resulting in the excellent characteristic in view of charge balance. Finally, we measured the properties of QLEDs with the WO3/NiOx bilayer to check the effects of the proposed device structure and showed the substantial improvement of the electrical conductivity of NiOx, the luminance, and the current efficiency of the QLEDs.  相似文献   
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康坊  杨飞然  杨军 《应用声学》2022,41(2):173-182
为了提高独立向量分析算法在盲语声分离任务中的分离性能,降低算法计算复杂度,并改善目前尚未完全解决的顺序模糊性的问题,该文提出一种基于子带t分布的快速独立向量分析算法。在声源模型方面,该算法首先利用语声信号重尾分布的特性,假设声源概率密度函数服从t分布,同时采用子带建模的方法来增强同一声源相邻频点的高阶依赖性,进而减轻频点间的顺序不一致问题。在空间模型方面,该算法采用秩1更新的方式估计声源信号,避免矩阵求逆操作和分离矩阵的估计,从而降低计算复杂度。实验结果表明,与现有的基于独立向量分析的盲源分离算法相比,该算法能够在相同的迭代次数下取得更优的语声分离性能。  相似文献   
8.
Standing surface acoustic wave (SSAW) based microfluidic devices have shown great promise toward fluid and particle manipulation applications in medicine, chemistry, and biotechnology. In this article, we present an analytical model for investigating continuous manipulation of particles (both synthetic and biological) within electroosmotic flow of non-Newtonian bio-fluids in a microfluidic channel under the influence of standing surface acoustic waves (SSAW). The particles are injected along the center of channel into the electroosmotically driven flow of power-law fluids, wherein their transport through the SSAW region is dictated by the hydrodynamic, electrophoretic, and acoustic forces. We first present a mathematical model to analyze the characteristics of electroosmotic flow of non-Newtonian power-law fluids in a hydrophobic slit microchannel. Next, we investigate the trajectories of particles in the flow field due to the combined effect of electroosmotic, electrophoretic, and acoustophoretic forcing mechanisms. The effect of key parameters such as particle size, their physical properties, input power, flow rate, and flow behavior index on the particle trajectories is examined while including the effect of the channel walls. The presented model delineates the methodologies of improving SSAW-based particle separation technology by considering the fluid rheology as well as the surface properties of the channel walls. Therefore, we believe that this model can serve as an efficient tool for device design and quick optimizations to explore novel applications concerning the integration of electroosmotic flows with acoustofluidic technologies.  相似文献   
9.
A novel type of magnetic molecularly imprinted polymer was prepared for the selective enrichment and isolation of chelerythrine from Macleaya cordata (Willd) R. Br. The magnetic molecularly imprinted polymers were prepared using functional Fe3O4@SiO2 as a magnetic support, chelerythrine as template, methacrylic acid as functional monomer, and ethylene glycol dimethacrylate as cross‐linker. Density functional theory at the B3LYP/6‐31G (d, p) level with Gaussian 09 software was applied to calculate the interaction energies of chelerythrine, methacrylic acid and the complexes formed from chelerythrine and methacrylic acid in different ratios. The structural features and morphology of the synthesized polymers were characterized by using Fourier transform infrared spectroscopy, X‐ray diffraction, transmission electron microscopy, and vibration sample magnetometry. Adsorption experiments revealed that the magnetic molecularly imprinted polymers possessed rapid kinetics, high selectivity, and a higher binding capacity (7.96 mg/g) to chelerythrine than magnetic molecularly non‐imprinted polymers (2.36 mg/g). The adsorption process was in good agreement with the Langmuir adsorption isotherm and pseudo‐second‐order kinetics models. Furthermore, the magnetic molecularly imprinted polymers were successfully employed as adsorbents for the extraction and enrichment of chelerythrine from Macleaya cordata (Willd) R. Br. The results indicated that the magnetic molecularly imprinted polymers were suitable for the selective adsorption of chelerythrine from complex samples such as natural medical plants.  相似文献   
10.
建立了以多糖衍生物为手性固定相的高效液相色谱-串联质谱(HPLC-MS/MS)直接拆分氰戊菊酯对映体的方法。在反相液相色谱条件下,考察了手性固定相的种类、流动相组成、柱温、流速对氰戊菊酯4个立体异构体分离的影响。同时,利用热力学方法对氰戊菊酯的立体异构体与固定相之间的色谱保留和分离的热力学机理进行了探讨。结果表明:采用Lux Cellulose-3(纤维素-三(4-甲基苯甲酸酯))手性色谱柱,在以流动相为乙腈-水(5 mmol/L甲酸铵)=(55:45,V:V)流速0.4 mL/min,柱温30℃的条件下,可在14 mins内实现氰戊菊酯4个立体异构体的基线分离。拓展了HPLC-MS/MS在菊酯类手性农药对映体分离及检测上的应用。  相似文献   
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