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991.
George Ting-Kuo Fey P. Muralidharan Cheng-Zhang Lu Yung-Da Cho 《Electrochimica acta》2006,51(23):4850-4858
An enhanced electrochemical performance LiCoO2 cathode was synthesized by coating with various wt.% of La2O3 to the LiCoO2 particle surfaces by a polymeric method, followed by calcination at 923 K for 4 h in air. The surface-coated materials were characterized by XRD, TGA, SEM, TEM, BET and XPS/ESCA techniques. XRD patterns of La2O3-coated LiCoO2 revealed that the coating did not affect the crystal structure, α-NaFeO2, of the cathode material compared to pristine LiCoO2. TEM images showed a compact coating layer on the surface of the core material that had an average thickness of about ∼15 nm. XPS data illustrated that the presence of two different environmental O 1s ions corresponds to the surface-coated La2O3 and core material. The electrochemical performance of the coated materials by galvanostatic cycling studies suggest that 2.0 wt.% coated La2O3 on LiCoO2 improved cycle stability (284 cycles) by a factor of ∼7 times over the pristine LiCoO2 cathode material and also demonstrated excellent cell cycle stability when charged at high voltages (4.4, 4.5 and 4.6 V). Impedance spectroscopy demonstrated that the enhanced performance of the coated materials is attributed to slower impedance growth during the charge-discharge processes. The DSC curve revealed that the exothermic peak corresponding to the release of oxygen at ∼464 K was significantly smaller for the La2O3-coated cathode material and recognized its high thermal stability. 相似文献
992.
993.
994.
Jyh-Luen Chen Ming-Shiu Lu Hui-Min Huang Feng-Chih Chang 《Journal of Polymer Research》1996,3(3):177-184
Bisphenol-A polycarbonate (PC) has been incorporated into epoxy resin cured with 4,4-diaminodiphenyl sulphone (DDS) and 4,4'-diaminodiphenyl methane (DDM). IR spectra reveal that transesterification and transamidation occur between the carbonate group of PC and the hydroxyl group of cured epoxy resin for the DDM-cured system, and that only transesterification occurs for the DDS-cured system. Scanning electron micrographs (SEM) show no evidence of phase separation in these cured systems, which is an indication of full miscibility between the bisphenol-A monomers and PC-oligomers with the copolymer network. The mechanical strength and glass transition temperature (Tg) fluctuate with PC content, whereas the flexural modulus shows a steadily increasing tendency. 相似文献
995.
Hong-Yang Lu Jong-Shing Bow Wen-How Deng 《Journal of the American Ceramic Society》1990,73(12):3562-3568
Pure BaTiO3 exhibits a paraelectric-to-ferroelectric phase transition at 130°C. When stoichiometric BaTiO3 is combined with 10 mol% ZrO2 , the relative permittivity (ε) changes to a broad, relatively insignificant temperature dependence, and the Curie point, T c , is not sharply defined. However, the transition sharpens at T = 95°C when these samples are sintered for a longer period of 60 h. SEM, EDAX analysis coupled with TEM observation gives three types of core-shell structures of different microstructural characteristics which are related to the diffuse phase transition. Chemical inhomogeneity, due to Zr4+ distribution in the core-shell structure, is proposed to account for the diffuse phase transition behavior. 相似文献
996.
电动螺旋轮胎定型硫化机的研究 总被引:2,自引:2,他引:2
介绍了电动螺旋轮胎定型硫化机的结构及原理。分析了对电动螺旋硫化机各项实验所得的数据。总结出该新型硫化机具有运动平稳、对中性好、精度高、结构紧凑、简单可靠、造价低、提高轮胎的硫化质量、便于维护保养等优点,值得推广。 相似文献
997.
Liang Xu Lei Su Hongjie Wang Min Niu Lei Zhuang Kang Peng Xingyu Fan Hongfei Gao De Lu 《Journal of the American Ceramic Society》2022,105(8):5490-5500
Pursuing novel thermal barrier–coating materials with lower thermal conductivity and high-temperature stability can simultaneously improve the working efficiency and service temperature of a gas turbine. In this study, a series of high-entropy RE2(Y0.2Yb0.2Nb0.2Ta0.2Ce0.2)2O7 (RE = La, Nd, Sm, Gd, Dy, and Er) oxides were prepared though solid-state reaction. Through tuning the rare-earth cations, an order–disorder transition occurs from certain partially ordered weberite structure (C2221) to disordered defective fluorite structure (Fm m). All the high-entropy RE2(Y0.2Yb0.2Nb0.2Ta0.2Ce0.2)2O7 oxides possess low thermal conductivity in the range of 0.91–1.34 W m−1 K−1 at room temperature, which can be attributed to increased lattice anharmonicity and disorder, resulting in additional phonon scattering. Herein, we proved that the incorporation of heterovalent cations at B-sites in high-entropy A2B2O7 crystals is an effective strategy to reduce the thermal conductivity without compromising the decrease of oxygen vacancy. Moreover, the high-entropy RE2(Y0.2Yb0.2Nb0.2Ta0.2Ce0.2)2O7 oxides show the relatively higher thermal expansion coefficients of 10.3–10.7 × 10−6°C−1 and excellent phase stability at elevated temperatures. 相似文献
998.
水库滑坡位移与水动力耦合预测参数及其评价方法研究 总被引:2,自引:0,他引:2
针对库水涨落诱发滑坡致灾机理,在系统分析水库边坡位移与库水位变化规律及其相互作用关系的基础上,运用弹塑性力学基本原理,提出了以库水位下降引起的边坡下滑动力增量作为边坡的加载动力参数,以相应边坡位移变化量作为边坡位移响应参数,以此确定水库边坡库水动力增载位移响应比参数并建立预测模型。运用动力增载位移响应比预测模型对三峡库区典型水库滑坡-黄土坡滑坡关键部位监测点进行了动力增载位移响应比计算,并采用Geostudio软件对该滑坡稳定性进行了数值模拟分析。该滑坡的位移响应特征与稳定性演化规律表明,该滑坡关键变形部位的动力增载位移响应比参数变化规律与其实际位移与稳定性演化规律基本吻合。研究结果表明了动力增载位移响应比参数是水库滑坡有效的位移动力评价参数,可运用该参数及其评价方法对水库滑坡进行稳定性分析与评价。 相似文献
999.
By means of the molecular dynamics (MD) simulation, the crystallization mechanism of 22,8-polyurethane which contains hydrogen-bond units is investigated and the results show that the crystallization process at a fixed temperature can be characterized by three stages: (1) The extended chain collapses to a globular random coil; (2) The random coil reorganizes into an ordered lamellar structure; (3) Accompanied with the segments clustering due to the hydrogen-bond formation, the lamellar develops with local defects. Two kinds of hydrogen-bond, which are formed between NH group and CO group (N-H?OC), and between NH group and urethane alkoxy oxygen (N-H?O), respectively, are found to play an important role in the crystallization process of 22,8-polyurethane. Furthermore, the effect of temperature on the crystallization is also studied by selecting three temperatures 200, 300 and 400 K. The lower the crystal temperature is, the slower the crystallization rate is and the stronger the hydrogen-bonding interactions are presented. This is in harmony with the experimental results. 相似文献
1000.