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101.
目前世界上普遍应用的配电系统消弧线圈接地方式在一定程度上保证了系统的供电可靠性,但仍然存在接地残流较大和高阻型故障检测难等问题。GFN(接地故障全中和器)具有消除接地电流、准确定位故障点,以及提升供电稳定性和可靠性的作用。介绍了瑞典GFN接地故障全补偿技术的基本原理、功能特点、应用实例和功能扩展等。实用情况表明GFN接地故障全补偿技术可以较为成功地减少特殊瞬时故障。 相似文献
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Yannick Hemberger Nadja Wichtner Christoph Berthold Klaus G. Nickel 《International Journal of Applied Ceramic Technology》2016,13(1):116-124
The relationship between Y2O3 content in tetragonal and cubic ZrO2 phases and the shift of the Raman band at ~645/cm was investigated. With increasing Y2O3 content, the 645/cm Raman band position decreases to lower Raman shift values. A fit of x = Y2O3 content in wt% and y = Raman band position in per cm, was found to be valid for low Y2O3‐stabilized t‐ZrO2, t′′‐ZrO2 transition, and fully stabilized c‐ZrO2. Modeling the change in lattice parameters due to the incorporation of Y2O3 in ZrO2 as obtained from Rietveld‐refined XRD data confirms that the peculiar sigmoidal form of the band shift with Y2O3 content is mainly due to a variation of the amount of oxygen vacancies. The resultant method is highly attractive in fields of Y2O3 determination in ZrO2 materials where a fast, spatially resolved, and nondestructive analysis is required. 相似文献
105.
Mesoporous MCM-41 silica spheres were prepared via the pseudomorphic route, using commercial prontosil silica spheres. Surface modification offers a great opportunity to adjust both the pore structure and surface properties of MCM-41 type materials which results in materials of improved hydrothermal and mechanical stability to make them promising candidates for chromatographic applications. In the present context, the obtained MCM-41 silica spheres were surface modified with octadecyl (C18) alkyl chains, by using direct grafting and surface polymerization methods, in order to vary the degree of surface hydrophobicity. The resulting materials were characterized before and after surface modification using various characterization techniques, with special emphasis on NMR and FTIR spectroscopies, for studying the attachment, mobility and the conformational order of the attached alkyl chains. 相似文献
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Organic alkyl and aryl phosphites are effective antioxidants and photostabilizers with applications in a wide range of polymers. The primary role of phosphites is to decompose hydroperoxide. However, aryl phosphites are also capable of reacting as antioxidants by affecting the kinetics. In particular, oligomer‐type phosphites have a greater effect on polymer degradation because of their high compatibility, reactivity, and solubility with almost all polymers. Generally, phosphites are sensitive to hydrolysis. In order to overcome this hydrolytic sensitivity in phosphites, a novel hydrolytically stable oligomeric phosphite incorporating a sterically hindered aromatic alcohol (2,4‐di‐tert‐butyl‐6‐methylphenol) that gives hydrolytic stability to the phosphite was synthesized and characterized, and its performance as an antioxidant for polypropylene was investigated. J. VINYL ADDIT. TECHNOL., 22:146–155, 2016. © 2014 Society of Plastics Engineers 相似文献
108.
Roland Mainz Alfons Weber Humberto Rodriguez‐Alvarez Sergiu Levcenko Manuela Klaus Paul Pistor Reiner Klenk Hans‐Werner Schock 《Progress in Photovoltaics: Research and Applications》2015,23(9):1131-1143
Ga segregation at the backside of Cu(In,Ga)Se2 solar cell absorbers is a commonly observed phenomenon for a large variety of sequential fabrication processes. Here, we investigate the correlation between Se incorporation, phase formation and Ga segregation during fast selenisation of Cu–In–Ga precursor films in elemental selenium vapour. Se incorporation and phase formation are analysed by real‐time synchrotron‐based X‐ray diffraction and fluorescence analysis. Correlations between phase formation and depth distributions are gained by interrupting the process at several points and by subsequent ex situ cross‐sectional electron microscopy and Raman spectroscopy. The presented results reveal that the main share of Se incorporation takes place within a few seconds during formation of In–Se at the top part of the film, accompanied by outdiffusion of In out of a ternary Cu–In–Ga phase. Surprisingly, CuInSe2 starts to form at the surface on top of the In–Se layer, leading to an intermediate double graded Cu depth distribution. The remaining Ga‐rich metal phase at the back is finally selenised by indiffusion of Se. On the basis of a proposed growth model, we discuss possible strategies and limitations for the avoidance of Ga segregation during fast selenisation of metallic precursors. Solar cells made from samples selenised with a total annealing time of 6.5 min reached conversion efficiencies of up to 14.2 % (total area, without anti‐reflective coating). The evolution of the Cu(In,Ga)Se2 diffraction signals reveals that the minimum process time for high‐quality Cu(In,Ga)Se2 absorbers is limited by cation ordering rather than Se incorporation. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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Nasir Mahmood Asad Ullah Khan Klaus Werner Stöckelhuber Amit Das Dieter Jehnichen Gert Heinrich 《应用聚合物科学杂志》2014,131(11)
This article reports the preparation and characterization of multiwalled carbon nanotubes (MWCNTs)‐filled thermoplastic polyurethane–urea (TPUU) and carboxylated acrylonitrile butadiene rubber (XNBR) blend nanocomposites. The dispersion of the MWCNTs was carried out using a laboratory two roll mill. Three different loadings, that is, 1, 3, and 5 wt % of the MWCNTs were used. The electron microscopy image analysis proves that the MWCNTs are evenly dispersed along the shear flow direction. Through incorporation of the nanotubes in the blend, the tensile modulus was increased from 9.90 ± 0.5 to 45.30 ± 0.3 MPa, and the tensile strength at break was increased from 25.4 ± 2.5 to 33.0 ± 1.5 MPa. The wide angle X‐ray scattering result showed that the TPUU:XNBR blends were arranged in layered structures. These structures are formed through chemical reactions of ? NH group from urethane and urea with the carboxylic group on XNBR. Furthermore, even at a very low loading, the high degree of nanotubes dispersion results in a significant increase in the electrical percolation threshold. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40341. 相似文献