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91.
研究了准贝氏体铸钢不同奥氏体温度正火对其组织与力学性能的影响 ,结果表明 ,随奥氏体化温度的提高 ,准贝氏体铸钢的强韧性改善 ,在 10 4 0℃正火 ,准贝氏体铸钢具有最佳强韧性配合。分析了高温奥氏体化正火强韧性提高的原因。  相似文献   
92.
针对焊接冷却过程中是否有卸载发生这一问题展开讨论,采用数值模拟方法研究在移动热源情况下钛合金焊接应力应变发展过程,给出钛合金焊接热弹塑性应力应变过程全图的定量物理描述.结果表明,钛合金焊接冷却过程中有卸载发生;钛合金焊接热弹塑性应力应变过程全图由熔化区、压缩塑性区、拉伸塑性区、卸载区、受压弹性区五部分构成;在力学熔化区等温线内的拉伸塑性区的范围包括焊缝和近缝区,但在残余状态焊缝和近缝区均为卸载区.  相似文献   
93.
将9SiCr钢的粒状原始组织改变为片状,再经830℃淬火后,其马氏体形态为筐篮编结状。而传统工艺所获得的马氏体形态为针状.这种筐篮编结状马氏体是9SiCr钢中一种崭新的组织形态,其精细结构为平行成束的板条。亚结构为高密度缠结位错.它有良好的综合机械性能,强韧性高,耐磨性高。  相似文献   
94.
磷酸铁(FePO4)是锂电池正极材料磷酸铁锂(LiFePO4)的核心前驱体,FePO4形貌及硫含量对合成的LiFePO4材料性能有重要影响。为得到类球形低硫FePO4产品,在传统液相沉淀法技术基础上做了改进优化,添加十六烷基三甲基溴化铵(CTAB)作为形貌助剂提高产品球形度,添加氨水作为配体形成磷酸铁铵配合物改善结晶过程,降低产品硫含量。结果表明:所制备的FePO4产品硫质量分数低,达到2.6×10 -5,形貌为均一的微米类球形颗粒,D50=11.4 μm,振实密度达到1.22 g/cm 3,有望成为制备高压实密度LiFePO4材料的核心前驱体。  相似文献   
95.
High‐molecular‐weight atactic poly(vinyl alcohol) (a‐PVA) gels loaded with (R,S)‐2‐(3‐benzoylphenyl)propionic acid (ketoprofen) were prepared from 5, 6, 7, and 8 g/dL solutions of a‐PVA with a number‐average degree of polymerization of 4000 in an ethylene glycol/water mixture with an aging method to identify the effect of the initial polymer concentration on the swelling behavior, morphology, and thermal properties of a‐PVA gels. Then, the release behavior of ketoprofen from a‐PVA gels was investigated. As the polymer concentration decreased, the ability for network formation decreased, and the degree of swelling of the a‐PVA gels increased. In addition, the enthalpy increased with an increase in the a‐PVA concentration, but the melting temperatures of the gels prepared at different initial polymer concentrations were the same; this indicated that tighter gel networks would be formed by a higher polymer chain density. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007  相似文献   
96.
Gas hydrate formation experiments were conducted with a methane-ethane mixture at 273.7 or 273.9 K and 5100 kPa and using water droplets or water contained in cylindrical glass columns. The effect of kinetic inhibitors and the water/solid interface on the induction time for hydrate crystallization and on the hydrate growth and decomposition characteristics was studied. It was found that inhibitors GHI 101 and Luvicap EG delayed the onset of hydrate nucleation. While this inhibition effects has been reported previously some unusual behaviour was observed and reported for the first time. In particular, the water droplet containing GHI 101 or Luvicap EG was found to collapse prior to nucleation and spread out on the Teflon surface. Subsequently, hydrate was formed as a layer on the surface. Catastrophic growth and spreading of the hydrate crystals was also observed during hydrate formation in the glass columns in the presence of the kinetic inhibitor. Finally, when polyethylene oxide (PEO) was added into the kinetic inhibitor solution the memory effect on the induction time decreased dramatically.  相似文献   
97.
Solutions of rare earth modifier (RES) and epoxy chloropropane (ECP) grafting modification method were used for the surface treatment of aramid fiber. Tensile properties of both the aramid/epoxy composites and single fibers were tested. The effects of RES concentration on tensile properties of aramid/epoxy composites were investigated in detail to explore an optimum amount of rare earth elements in solution for modifying aramid fiber. The fracture surface morphologies of tensile specimens were observed and analyzed with the aid of SEM. The experimental results show that rare earth treatment is superior to ECP grafting treatment in promoting interfacial adhesion between the aramid fiber and epoxy matrix. Meanwhile, the tensile strengths of single fibers were almost not affected by RES treatment. The optimum performance is obtained when the content of rare earth elements is 0.5 wt %. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1037–1041, 2004  相似文献   
98.
Catalytic activity of a 1 wt% Au/TiO2 catalyst is markedly improved by loading a large amount of FeOx, on which the oxidation of CO in excess H2 is selectively promoted at temperature lower than 60 °C. Oxidation of CO with O2 on the FeOx/Au/TiO2 catalyst is markedly enhanced by H2, and H2O moisture also enhances the oxidation of CO but its effect is not so large as the promotion by H2. We deduced that activation of Au/TiO2 catalyst by loading FeOx is not caused by the size effect of Au particles but a new reaction path via hydroxyl carbonyl intermediate is responsible for the superior activity of the FeOx/Au/TiO2 catalyst.  相似文献   
99.
In this paper, we propose a computational framework to incorporate regularization terms used in regularity based variational methods into least squares based methods. In the regularity based variational approach, the image is a result of the competition between the fidelity term and a regularity term, while in the least squares based approach the image is computed as a minimizer to a constrained least squares problem. The total variation minimizing denoising scheme is an exemplary scheme of the former approach with the total variation term as the regularity term, while the moving least squares method is an exemplary scheme of the latter approach. Both approaches have appeared in the literature of image processing independently. By putting schemes from both approaches into a single framework, the resulting scheme benefits from the advantageous properties of both parties. As an example, in this paper, we propose a new denoising scheme, where the total variation minimizing term is adopted by the moving least squares method. The proposed scheme is based on splitting methods, since they make it possible to express the minimization problem as a linear system. In this paper, we employed the split Bregman scheme for its simplicity. The resulting denoising scheme overcomes the drawbacks of both schemes, i.e., the staircase artifact in the total variation minimizing based denoising and the noisy artifact in the moving least squares based denoising method. The proposed computational framework can be utilized to put various combinations of both approaches with different properties together.  相似文献   
100.
Zinc vaporization of Mn-Zn ferrites was quantitatively characterized in terms of oxygen partial pressure P O2, temperature, grain size and sample geometry. The amount of zinc loss was measured as a function of time at various temperatures by a thermogravimetric method. The weight loss due to irreversible zinc vaporization showed a linear behavior with time and increased exponentially with temperature. The observed weight loss due to zinc evaporation at 1100°C was small, whereas a significant weight change was detected at 1200°C. The weight loss was even greater in a reducing atmosphere ( P O2= 5 × 10−5). Below 1300°C, the diffusion of elemental zinc was sufficiently fast to compensate the zinc loss at the interface region, resulting in a linear dependence on time. At temperatures ≥1400°C, the weight change no longer followed the linear dependence and showed a rather parabolic behavior with a concave upward slope. The core shape and the gas flow around ferrite cores were important factors that affected the rate of zinc vaporization, but not the grain size.  相似文献   
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