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181.
微孔发泡过程中聚合物/超临界CO2均相体系形成的研究   总被引:4,自引:0,他引:4  
阐述以超临界CO2为发泡剂的微孔发泡中均相体系的形成过程,研究聚合物熔体和气体的混合机理,并分析影响均相体系形成过程的因素。结果表明,聚合物和气体本身的结构和性质、工艺条件、加工设备、外力场等均影响均相体系的形成,振动力场的引入可以提高多相体系的混合程度,在聚合物/气体均相体系的形成过程中引入振动力场是一个全新的研究方向。  相似文献   
182.
作者对精细化工发展的策略提出如下意见:①将项目为核心改成以技术为核心;②培植企业和部门的技术力量;③搞好行业内部、行业之间、企业内部的协调;④产品方案向横向、纵向延伸;⑤采取多种技术引进方式。  相似文献   
183.
Brominated poly(isobutylene-co-4-methylstyrene) (BIMS) is a synthetic terpolymer which can be stoichiometrically cross-linked by N,N′-dicinnamylidene-1,6-hexanediamine (DIAK). The degree of cross-links on bulk samples was determined by measuring the low frequency shear modulus with parallel plate method. The surface modulus of the same samples was measured using a new method, shear modulation force microscopy (SMFM). The moduli of the bulk sample and the surface were found to have the same scaling with the cross-link density, and good agreement with rubber elasticity theory was obtained in both cases. The SMFM was then used to monitor the cross-linking process, as a function of DIAK concentration and curing time, in thin films where standard rheological methods cannot be applied. The results show that in all cases the cross-linking reaction at the surface reaches saturation in less than 10 min as compared to at least 1 h in the bulk samples.  相似文献   
184.
Matthew F. Paige 《Polymer》2003,44(20):6345-6352
Three different forms of atomic force microscope (AFM) measurement, topography, friction force and phase imaging, have been used to investigate the surface morphology and local composition of an immiscible polystyrene (PS)/poly(methyl methacrylate) (PMMA) blend film. This sample forms discrete, micron-size domains in a continuous matrix, which is attributed to the segregation of PMMA in PS. When the samples were imaged in air, contrast in friction and phase images was caused by variations in sample topography only. When the samples were imaged under water, however, both friction and phase imaging yielded non-topographic contrast between domains. We ascribe the contrast in both of these imaging modes to preferential softening of the hydrophilic, PMMA-rich domains and to stronger tip-sample adhesive forces, highlighting the AFM's utility for probing local elastic properties and for compositional mapping of soft polymer samples.  相似文献   
185.
Both confocal Raman microspectroscopy and atomic force microscopy (AFM) have been undertaken to study the crystalline and the morphological aspects of cast PA 6 films at a sub-microscopic scale. The percentages of the different crystalline structures present within PA 6 cast films, i.e. the monoclinic α, the pseudo-hexagonal β, and the monoclinic γ, have been measured by confocal Raman microspectroscopy. In cast films, the prevailing structure is the β one. AFM has been used to characterize the morphology of the PA 6 films. Simultaneously, the deformed state has been considered as well. Our main interest has been to follow the evolution of the percentage of each crystalline structure as a function of the plastic deformation mechanisms which are responsible of the yielding of PA 6 films: shear banding for temperatures T lower than 160 °C and formation of fibrils for   相似文献   
186.
Structured dispersion particles suitable for pressure sensitive adhesives (PSA) were synthesized via swelling polymerization technique (EP 359562). Particles consisting of poly(n‐butyl acrylate) copolymerized with different types of carboxylic acids were used as seeds. The final particles were synthesized by swelling polymerization process, using 6 wt % styrene or 6 wt % methyl methacylate. The resulting particle morphology was analyzed by atomic force microscopy (AFM) and transmission electron microscopy (TEM). From previous works (Coll Surf A 2001, 183–185, 725–737; J Appl Polym Sci 2004, 91, 2610–2623) where two‐step emulsion polymerization was used on similar particles, it is expected that the particle morphology is affected by the polarity of the monomer used for swelling polymerization because of the phase compatibility (thermodynamic parameter). In this work, the seed particles used were always of a glass transition temperature (Tg) below polymerization temperature. The diffusion of the growing polymer chains from the swelling polymerization is therefore mainly affected by their own Tg and the influence of the carboxy groups on the chain length of the entering radicals (kinetic parameter). The different morphologies of the single particles are discussed qualitatively. The effects of reaction parameters are compared with the results given in the previous work. The structure of the corresponding dispersion films was characterized using AFM. Correlations to macroscopic properties such as the cohesive strength and peel adhesion to different substrates are discussed. The results are also compared with the application properties of the corresponding unmodified particles, statistical copolymers, and to blends with small sized PMMA or PS particles. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1444–1455, 2006  相似文献   
187.
Electropolymerization of pyrrole on lead substrate electrode was studied. Due to electrochemical activity of Pb in acidic media, this process is only possible at basic pHs. For this purpose, electropolymerization process was performed in an aqueous solution of Na2SO4 with pH 12. Potentiodynamic cycling shows the Pb oxidation at the first cycles. In subsequent cycles, polypyrrole film grows on the oxidized lead substrate. Of course, as the passive film is highly porous, a composite of polypyrrole/PbSO4 is formed in the first layers. However, subsequent cycling leads to the formation of pure polypyrrole film. According to this structure and strong connection of the polymer film to the substrate surface via this composite layer, the polypyrrole film deposited on the lead surface has enhanced mechanical stability. AFM measurements showed peculiar smoothness of both composite and lateral polypyrrole films. This synthesis approach is of particular interest for the preparation of highly stable polymer films and fabrication of supercapacitors with a polymer/PbSO4 conductive structure.  相似文献   
188.
Data on the growth of cracks tested in aqueous solutions were interpreted in terms of surface force theory. For applied stress intensity factors greater than 0.25 MPa · m½, the position and the slope of the curves and their dependence on pH and ion concentration can be explained in terms of surface force theory, provided these forces are of a magnitude and range that are representative of those involved in the cohensive bonding of solids. Weaker forces, such as structural, double-layer, or dispersion forces, have little effect on crack growth in silica glass for K I > 0.25 MPa · m½.  相似文献   
189.
根据6自由度施釉机器人的终端受力,利用雅可比矩阵,求解出各转动关节在稳定平衡状态下的受力和所需的驱动力矩,为设计施釉机器人确定各转轴的电机及其他动力元件提供了可靠的依据。  相似文献   
190.
Drag force is a key parameter in the numerical modeling of gas-particle flow in circulating fluidized beds. The reliability of current drag force correlations over the regime of fast fluidization has, however, not been thoroughly investigated. In this article, a drag force correlation accounting for the clustering effects for Geldart A particles is used to simulate the behaviors typical of fast fluidization, including dynamic evolution of clusters as well as time- averaged axial and lateral voidage profiles. Diverse images of clusters are captured and the time-averaged profiles of voidage are shown to be in quantitative agreement with the present empirical correlation. The results based on different constitutive correlations of drag force show the importance of the choice of drag force in modeling fast-fluidized beds. This drag force correlation, based on a simple averaging assumption, could give some basic insights about the magnitude of the drag reduction.  相似文献   
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