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51.
高温炉内的辐射传热是工业生产中常遇到的问题。过去,人们在应用热流法计算辐射传热时遇到了一定的困难,使计算结果与实际有一定的偏差。本文运用文献[1]中给出的新热流数学模型,开发出由新热流方程与能量方程相耦合的计算机程序,其中的比热流参数由线加热热源情况下计算得到。用该程序计算了实验室用马弗炉内的温度场,并且用热电偶实测了炉内的一些温度值,理论计算与实测值符合很好。 相似文献
52.
53.
将空气中烧成的镍导体用于散热制冷片制作工艺中,可降低成本,提高合格率。通过实验得到的最佳值为:镍导体中4号玻璃(SiO2>30,B2O3>10,PbO<55,TiO2少许)的含量4.5%,化学镀镍时间50min,方阻47.5mΩ/□,附着力8.1N/mm2。 相似文献
54.
钛酸铅系薄膜的热释电性能及其应用 总被引:10,自引:1,他引:9
叙述了钛酸铅系薄膜的热释电原理,介绍了国际上近几年钛酸铅系薄膜材料、制备工艺及热释电性能,并与块状陶瓷材料进行了比较,分析表明钛酸铅系薄膜具有优良的热释电性能及可观的应用前景。 相似文献
55.
Wu Ting M. Badaye T. Morishita N. Koshizuka S. Tanaka 《Journal of Superconductivity》1996,9(6):637-645
Recently, superconducting Nd1Ba2Cu3Oy (Ndl23) thin films with high superconducting transition temperature (T
c) have been successfully fabricated at our institute employing the standard laser ablation method. In this paper, we report the results of surface characterization of the Nd123 thin films using an ultrahigh vacuum scanning tunneling microscope/spectroscopy (UHV-STM/STS) and an atomic force microscope (AFM) system operated in air. Clear spiral pattern is observed on the surfaces of Nd123 thin films by STM and AFM, suggesting that films are formed by two-dimensional island growth mode. Contour plots of the spirals show that the step heights of the spirals are not always the integer or half-integer number of thec-axis parameter of the structure. This implies that the surface natural termination layer of the films may not be unique. This result is supported byI-V STS measurements. The surface morphology of the Nd123 thin films is compared with that of thec-axis-oriented Y1Ba2Cu3Sy thin films. Surface atomic images of the as-prepared Nd123 thin films are obtained employing both STM and AFM. STS measurements show that most of the surfaces are semiconductive. The results of STS measurements together with the fact that we are able to see the surface atomic images using scanning probe microscopes suggest that exposure to air does not cause serious degradation to the as-prepared surfaces of Nd123 thin films. 相似文献
56.
Pankaj Mathure Ashwin Patwardhan 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2005,80(4):413-419
In this study, the mass transfer efficiencies of a novel horizontal rotating packed (h‐RPB) bed and the conventional disc‐type rotating biological contactor (RBC) were studied at four speeds and seven submergences. Pall rings of two different sizes (25, 38 mm), superintalox saddles and a wiremesh spiral bundle were used as packings in the h‐RPB. Volumetric gas–liquid mass transfer coefficients were determined by unsteady state absorption of atmospheric oxygen in de‐aerated water. Power consumption per unit liquid volume has been found for all geometries tested. The oxygen transfer efficiency values for the h‐RPB were found to be 2–5 kg kWh?1 and for the disc RBC were found to be 1–2 kg kWh?1. The performance of the h‐RPB was also compared with other gas–liquid contactors such as surface aerators. The study proves that the h‐RPB is a energy efficient alternative to conventional contactors. Copyright © 2005 Society of Chemical Industry 相似文献
57.
58.
飞行时间二次离子质谱--强有力的表面、界面和薄膜分析手段 总被引:8,自引:0,他引:8
二次离子质谱(Secondary ion mass spectrometry,简称SIMS)是一种对表面灵敏的质谱技术,建立在表面各种类型带正、负电荷原子或分子发射的基础上。用飞行时间(Time of flight,简称TOF)仪器对这些二次离子进行质量分析,能确保并行质量登录、高质量范围、高流通率下的高分辨和精确质量测定这些优异性能。配合细聚焦扫描一次离子束,可在优于1nm的高深度分辨和优于50nm的横向分辨本领下,实现对表面优于单层ppm(百万分之一)量级的极高检测灵敏度。当今TOF-SIMS已发展为一种成熟且完善的表面分析技术。极高的灵敏度,再加上即使对大分子及不易挥发性分子都独具的敏感性,使它成为很多高技术领域不可缺少的分析手段,这些领域包括微电子学、化学和材料科学以至纳米技术和生命科学等。本文简述了TOF-SIMS的原理、仪器及其多方面的应用和展望。 相似文献
59.
M. M. Rashid 《International journal for numerical methods in engineering》2002,55(4):431-450
A computational procedure for remapping material state information from one finite element mesh to another is described. The procedure is useful in connection with evolving meshes for inelastic problems, as for example occur in the context of fracture simulation and adaptive mesh refinement. The proposed method is based on weak enforcement of equality between corresponding fields on the two meshes, where piecewise‐constant fields on both meshes are generalized from the quadrature‐point values. The essential algorithmic problem is that of calculating the volume partition of an arbitrary convex region with respect to a covering set of disjoint convex regions. Instead of geometrically resolving the associated intersections, the problem is herein approximated by a constrained optimization problem, which may be readily and efficiently solved computationally. This formulation is a main contribution of the paper. Computational examples are given that illustrate the effectiveness of the proposed procedure. Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
60.
Wenwei He Wuping Liao Weiwei Wang Deqian Li Chunji Niu 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2008,83(9):1314-1320
BACKGROUND: Thermodynamics and kinetics data are both important to explain the extraction property. In order to develop a novel separation technology superior to current extraction systems, many promising extractants have been developed including calixarene carboxylic acids. The extraction thermodynamics behavior of calix[4]arene carboxylic acids has been reported extensively. In this study, the mass transfer kinetics of neodymium(III) and the interfacial behavior of calix[4]arene carboxylic acid were investigated. RESULTS: The rate constant (Kao) becomes constant when the stirring speed was controlled between 250 rpm and 400 rpm. The activation energy (Ea) was calculated to be 21·41 kJ mol?1 or 88·17 kJ mol?1 (dependent on temperature) from the slope of log Kao against 1000/T. The linear relationship between the specific area and the extraction rate is the characteristic of an interfacial reaction control. The minimum bulk concentration of the extractant necessary to saturate the interface (Cmin) is lower than 4·19 × 10?4 mol L?1. CONCLUSION: The effect of stirring speed, temperature, and species concentration on the extraction rate demonstrates that the extraction regime depends on the extraction conditions. The chemical reaction control governs the extraction regime at temperatures below 303 K and a mixed control regime occurs when the temperature is between 303 K and 318 K. The probable locale for the chemical reaction is at the liquid–liquid interface and the rate equation is deduced to be: ? d[Nd3+](a)/dt = kf[Nd3+](a)[H4A](o)0·727[H+](a)?0·978. The rate‐controlling step was suggested by the analysis of the experimental results. Copyright © 2008 Society of Chemical Industry 相似文献