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991.
以氧化铬和石墨粉为原料,采用聚乙烯醇粘接,压制成阴极片,以光谱石墨棒为阳极,在800℃氯化钙熔盐中,恒电压3.2V下,阴极片自烧结电解制备碳化铬.采用XRD、SEM和EDX对样品进行表征.结果表明:粘接的阴极片满足熔盐电解的强度要求,通过熔盐电解过程的自烧结阴极片有效地粘接在一起,并制备出具有良好烧结性能、组分单一的Cr3C2粉体.该法制备Cr3C2的电流效率不低于37.3%.采用恒电位电解法和循环伏安法对电解机制的研究表明,熔盐电解制备Cr3C2的反应机制为:Cr2O3+e→Cr+O2-,Cr+C→Cr3C2两步完成. 相似文献
992.
介绍了用原子荧光光度计测定水中汞的方法。对检测结果进行分析,发现相较于双硫腙分光光度法和冷原子吸收法测定汞,荧光法有快速、简便、灵敏度高、干扰少、线性范围宽、检测限低等优点。 相似文献
993.
薄板在爆炸冲击载荷作用下的动力行为复杂,具有大变形、瞬时性、高度非线性等特点.当冲击波冲量较小时,薄板容易发生异常动力响应.然而,爆炸冲击波特征对薄板异常动力响应的影响尚不明晰.为此,本文采用经实验数据验证的自主开发爆炸载荷模型,首先成功地模拟了方形薄板的反直观异常动力响应;然后通过数值仿真研究了冲击波负压描述方法、正... 相似文献
994.
Y. Zhai R. Feder A. Brooks M. Ulrickson C.S. Pitcher G.D. Loesser 《Fusion Engineering and Design》2013,88(6-8):547-550
ITER diagnostic port plugs perform many functions including structural support of diagnostic systems under high electromagnetic loads while allowing for diagnostic access to the plasma. The design of diagnostic equatorial port plugs (EPP) are largely driven by electromagnetic loads and associate responses of EPP structure during plasma disruptions and VDEs. This paper summarizes results of transient electromagnetic analysis using Opera 3d in support of the design activities for ITER diagnostic EPP. A complete distribution of disruption loads on the diagnostic first walls (DFWs), diagnostic shield modules (DSMs) and the EPP structure, as well as impact on the system design integration due to electrical contact among various EPP structural components are discussed. 相似文献
995.
矸石充填是当前煤矿生产中常用的一种充填方式,用于液压支架后部的矸石捣实机构是充填工作的关键设备。矸石捣实机构有单级捣实机构和双级捣实机构,其支撑方式有下部推拉及上部吊挂等多种形式。根据现场使用经验,对结构进行了分析,并对充填开采方法提出一点建议。 相似文献
996.
A large amount of TiC hexagonal platelets has formed on the surface of the sample made of Ti/Si/TiC/Al0.2 after sintering at above 1450 °C in an Ar atmosphere. The basal plane of TiC platelets is (111) facet confirmed by X-ray diffraction. Small amounts of Si and Al elements dissolved in the TiC crystal structure, influencing the structure of TiC. The detailed structure and growth mechanism of the TiC platelets have been observed and analyzed. A model has been proposed to understand the formation of TiC hexagonal platelets. 相似文献
997.
Daishuang Li Jing Peng Maolin Zhai Jinliang Qiao Xiaohong Zhang Genshuan Wei 《应用聚合物科学杂志》2008,109(4):2071-2075
By using in situ prepolymerization and radiation curing, high‐impact polystyrene (HIPS) with a bimodal distribution of the size of the rubber particles (bimodal HIPS) was synthesized in the presence of ultrafine full‐vulcanized powdered styrene–butadiene rubber (UFPSBR) and polybutadiene rubber (BR). TEM photographs indicated that UFPSBR was dispersed uniformly as a single particle with a diameter of about 100 nm. On the other hand, bimodal HIPS with different rubber particle size distributions could also be obtained by blending HIPS and UFPSBR grafting styrene (UFPSBR‐g‐St) with different grafting yields. The bimodal HIPS with the smallest rubber particle size, at about 100 nm, could be prepared by blending the monomodal HIPS containing big rubber particles with polystyrene/UFPSBR. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
998.
Feng Xu Run‐Cang Sun Mei‐Zhi Zhai Jin‐Xia Sun Jian‐Xin Jiang Guang‐Jie Zhao 《应用聚合物科学杂志》2008,108(2):1158-1168
Six lignin fractions from mild ball‐milled Tamarix austromogoliac (TA) and Caragana sepium (CS) were sequentially isolated with 80% dioxane containing 0.05M HCl at 75°C for 4 h, 50% aqueous ethanol containing 1M triethylamine at 70°C for 4 h, and 8% aqueous NaOH at 45°C for 3 h. The results showed that the successive treatments made it possible to isolate lignin from wood with a high yield and purity, in which 89.4 and 90.6% of the original lignin from TA and CS were released, respectively. The lignin fractions isolated with the three‐step method were analyzed with Fourier transform infrared, 1H‐ and 13C‐NMR, alkaline nitrobenzene oxidation, and gel permeation chromatography. It was found that the three lignin fractions isolated from TA were rich in syringyl units, and the molar ratio of the relatively total moles of vanillin, vanillic acid, and acetovanillin to the relatively total moles of syringaldehyde, syringic acid, and acetosyringone decreased from 1: 2.6 to 1 : 3.2 to 1: 3.6 in the lignin preparations, whereas this ratio in the corresponding lignin fractions isolated from CS was found to be 1.4 : 1, 1.1 : 1, and 1 : 1.4, respectively. More importantly, the results revealed that the sequential extractions of the mild ball‐milled TA and CS with 80% acidic dioxane, 50% alkaline ethanol, and 8% aqueous NaOH under the conditions used did not significantly cleave the β–O‐4 and α–O‐4 linkages in lignin macromolecules. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
999.
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