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991.
The supramolecular 1 : 1 host–guest inclusion compound, p-tert-butylcalix[4]arene ·α,α,α-trifluorotoluene, 1, is characterized by 19F and 13C solid-state NMR spectroscopy. Whereas the 13C NMR spectra are easily interpreted in the context of earlier work on similar host–guest compounds, the 19F NMR spectra of solid 1 are, initially, more difficult to understand. The 19F{1H} NMR spectrum obtained under cross-polarization and magic-angle spinning conditions shows a single isotropic resonance with a significant spinning sideband manifold. The static 19F{1H} CP NMR spectrum consists of a powder pattern dominated by the contributions of the anisotropic chemical shift and the homonuclear dipolar interactions. The 19F MREV-8 experiment, which minimizes the 19F–19F dipolar contribution, helps to identify the chemical shift contribution as an axial lineshape. The full static 19F{1H} CP NMR spectrum is analysed using subspectral analysis and subsequently simulated as a function of the 19F–19F internuclear distance (DFF = 2.25 ± 0.01 Å) of the rapidly rotating CF3 group without including contributions from additional libration motions and the anisotropy in the scalar tensor. The shielding span is found to be 56 ppm. The width of the centerband in the 19F{1H} sample-spinning CP NMR spectrum is very sensitive to the angle between the rotor and the magnetic field. Compound 1 is thus an attractive standard for setting the magic angle for NMR probes containing a fluorine channel with a proton-decoupling facility.  相似文献   
992.
机械能守恒定律服从力学相对性原理   总被引:11,自引:1,他引:10  
阐述了机械能守恒定律服从力学相对性原理。  相似文献   
993.
The spin-wave excitations in anisotropic Kondo lattice model are studied using the spin Green's function. Both the ferromagnetic and antiferromagnetic cases are considered. The equations to determine the spectrum of low-energy excitations are given. The anisotropy gaps are obtained, and the long-wavelength and strong-coupling limits are analyzed.  相似文献   
994.
The dependence of the formation of the nanocrystalline bcc-Fe phase on the alloy composition is studied for Fe80M7B12Cu1 (M: Ti, Ta, Nb, Mo) alloys. The rf-Mössbauer technique is used to determine the optimal soft magnetic properties. This technique allowed us to compare anisotropy fields in each phase present in the composite alloys. The smallest anisotropy field was found in the bcc-Fe nanograins formed in Nb- and Mo-containing alloys.  相似文献   
995.
针对忽略岩土体非均质和各向异性将导致边坡稳定性评价产生误差的问题,应用极限分析上限理论及抗剪强度系数折减法,推导土体强度非均质和各向异性影响下隧道洞口含裂缝仰坡稳定性解析式,探究土体强度非均质和各向异性对仰坡稳定性系数、坡顶裂缝位置、隧道拱顶失稳范围及仰坡安全系数的影响。结果表明,裂缝深度及坡角越大,仰坡稳定性系数越小;非均质系数越大和各向异性系数越小,维持仰坡稳定的临界坡高越大;非均质系数及各向异性系数越大,裂缝距坡顶边缘越远,隧道拱顶失稳范围越大;非均质系数增大有利于仰坡稳定,而各向异性系数越大仰坡越易失稳。  相似文献   
996.
陡倾滑面滑坡推力竖向分力显著,基于滑坡推力水平假定与普通抗滑桩相互作用不充分这一问题,建立锯齿形抗滑桩结构。依据梯形分布滑坡推力的假设,推导了受荷段内力计算公式,采用Winkler弹性地基理论推导了锚固段内力计算公式,并开展锯齿形抗滑桩的力学性能研究。分析表明,(1)随着滑面倾角的增加,锯齿形抗滑桩的受荷段、锚固段的弯矩、剪力以及侧应力均减小,内力减小幅度随之增大;(2)滑面倾角在20°~40°时,随着滑面倾角的增加,锚固段的理论最小长度在逐渐增加,40°时锚固段的长度为4.2 m达到最大值,且该长度仅占整个桩长35%,远小于按现行规范取得的锚固段长度最大值(1/2总桩长),桩侧摩阻力就可以完全满足竖向力学平衡;(3)将锯齿形抗滑桩与普通抗滑桩内力对比,受荷段和锚固段的弯矩减小34%、剪力减小36%及桩侧应力减小幅度大于30%,力学性能良好。  相似文献   
997.
This work developed novel jute-yarn, non-crimp, unidirectional (UD) preforms and their composites, with three different types of warp jute yarns of varying linear densities and twists in the dry UD preforms, in order to present a possible solution to the detrimental effects of higher yarn twists and crimp at the warp–weft yarn interlacements of traditional, woven, preform-based composites on their mechanical properties. In the developed UD preforms, warp jute yarns were placed in parallel by using a wooden picture-frame pin board, with the minimal number of glass weft yarns to avoid crimp at the warp–weft yarns interlacements, which can significantly enhance the load-bearing ability of UD composites compared to traditional, woven, preform composites. It was found that an optimal combination of jute warp yarn linear densities and twists in the UD preforms is important to achieve the best possible mechanical properties of newly developed UD composites, because it encourages a proper polymer-matrix impregnation on jute fibres, leading to excellent fibre–matrix interface bonding. Composites made from the 25 lb/spindle jute warp yarn linear density (UD25) exhibited higher tensile and flexural properties than other UD composites (UD20, UD30). All the UD composites showed a much better performance compared to the traditional woven preform composites (W20), which were obviously related to the higher crimp and yarn interlacements, less load-carrying capacity, and poor fiber–matrix interfaces of W20 composites. UD25 composites exhibited a significant enhancement in tensile modulus by ~232% and strength by ~146%; flexural modulus by 138.5% and strength by 145% compared to W20 composites. This reveals that newly developed, non-crimp, UD preform composites can effectively replace the traditional woven composites in lightweight, load-bearing, complex-shaped composite applications, and hence, this warrants further investigations of the developed composites, especially on long-term and dynamic-loading mechanical characterizations.  相似文献   
998.
The preparation and characterization of biodegradable films based on starch-PVA-nanoclay by solvent casting are reported in this study. The films were prepared with a relation of 3:2 of starch:PVA and nanoclay (0.5, 1.0, and 1.5% w/v), and glycerol as plasticizer. The nanoclays before being incorporated in the filmogenic solution of starch-PVA were dispersed in two ways: by magnetic stirring and by sonication. The SEM results suggest that the sonication of nanoclay is necessary to reach a good dispersion along the polymeric matrix. FTIR results of films with 1.0 and 1.5% w/v of sonicated nanoclay suggest a strong interaction of hydrogen bond with the polymeric matrix of starch-PVA. However, the properties of WVP, tensile strength, percentage of elongation at break, and Young’s modulus improved to the film with sonicated nanoclay at 0.5% w/v, while in films with 1.0 and 1.5% w/w these properties were even worse than in film without nanoclay. Nanoclay concentrations higher than 1.0 w/v saturate the polymer matrix, affecting the physicochemical properties. Accordingly, the successful incorporation of nanoclays at 0.5% w/v into the matrix starch-PVA suggests that this film is a good candidate for use as biodegradable packaging.  相似文献   
999.
佘少华 《力学与实践》2005,27(2):57-59,69
利用全自动洗衣机高速脱水时产生的向心力,将衣物上的水沿脱水桶壁向下排出,由此设计了节水型洗衣机,并对这种洗衣机进行了力学原理分析,给出了关键结构参数,以及关键部件——排水阀的设计.新型洗衣机结构简单,洗涤容量进一步扩大,减少了水和洗涤剂的用量,有利于环境保护.  相似文献   
1000.
Solid‐state NMR and dynamic mechanical (DMA) measurements were performed on a series of uniaxially hot‐drawn bisphenol‐A polycarbonate samples in order to determine the effects of stretching on the structure, mobility, and local orientation environment. Proton spin‐lattice relaxation times, 1H T, for the phenylene carbon protons were fitted to a biexponential decay function, and both the long and short relaxation times initially increased with stretching. Intensity data indicated an increase in the number of short relaxation time protons and a decrease in the number of long relaxation protons with orientation. Similarly, DMA spectra showed that the β‐relaxation strength also increased with drawing, which implied an increase in the number of localized segmental relaxations. It is theorized that the long and short 1H T relate to protons within tightly packed “cooperative domains,” and to those with greater localized free‐volume, respectively. Stretching is known to distort the free‐volume distribution, causing a decrease in the mean free‐volume but an increase in the number of larger, more elliptical holes. This is expected to cause a decrease in the α‐transition mobility (due to larger cooperative domains) and an increase in the β‐mobility (due to the increase in the number of β‐relaxing segments associated with the larger free‐volume holes). These predictions are consistent with results recently reported by Shelby and Wilkes on the physical aging and creep behavior of these samples (M. D. Shelby & G. L. Wilkes, Polymer 1998, 39, 6767; M. D. Shelby & G. L. Wilkes, J Polym Sci Part B: Polym Phys 1998, 36, 2111). © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 32–46, 2001  相似文献   
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