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101.
在Einstein制冷循环系统中,气泡泵竖直提升管内为弹状流时效率较高。选取VOF(流体体积函数)模型对其管内气泡的运动状态进行计算流体力学数值模拟。结果表明:当过热度恒定时,随着压力增加,单个气泡的生成时间延长且体积变小,但气泡均匀性提高;当压力恒定时,随着过热度增大,气泡生成速率加快,融合体积增大,易于形成系统所需的弹状流。因此,在Einstein制冷循环系统中,在压力为0.4 MPa的工况下,需采取较高的过热度才能保证气泡泵的正常运转;与水相比,氨水溶液更适合作为气泡泵工质。 相似文献
102.
103.
Computational continua for linear elastic heterogeneous solids on unstructured finite element meshes
《International journal for numerical methods in engineering》2018,115(4):501-530
The computational continua framework, which is a variant of higher‐order computational homogenization theories that is free of scale separation, does not require higher‐order finite element continuity, and is free of higher‐order boundary conditions, has been generalized to unstructured meshes. The salient features of the proposed generalization are (i) a nonlocal quadrature scheme for distorted elements that accounts for unit cell distortion in the parent element domain and (ii) an approximate variant of the nonlocal quadrature that eliminates the cost of computing positions of the quadrature points in the preprocessing stage. The performance of the computational continua framework on unstructured meshes has been compared to the first‐order homogenization theory and the direct numerical simulation. 相似文献
104.
本文立足于太赫兹波成像领域近年来备受关注的研究热点—太赫兹波计算鬼成像,首先回顾了鬼成像从量子到经典再到计算的历史过程,然后阐述了计算鬼成像的数学原理,随后综述了计算鬼成像在太赫兹波段的发展历程,及其在超衍射分辨成像、石墨烯光电导成像、太赫兹光谱成像等方面的应用,并在最后展望了太赫兹波计算鬼成像的发展前景:计算鬼成像作为一种成像手段,可以绕开在太赫兹频段缺乏经济高效的焦面阵列式探测器的难题,但目前的成像帧率还难以满足快速成像的应用需求,相信在未来随着器件性能的提升和成像算法的优化,其成像帧率可以得到大幅提升。 相似文献
105.
作为太赫兹技术中的重要组成部分,太赫兹脉冲焦平面成像一经问世就引起了行业内的广泛关注,人们引入了各种方法去提升此成像技术的测量性能,同时也尝试将此成像技术应用于不同的工业和基础研究领域。本文综述了近年来人们对太赫兹脉冲焦平面成像的技术改良和应用研究,包括提升成像系统的空间分辨率、信噪比、信息获取能力,以及将此成像技术应用于光谱识别检测、超表面器件功能验证、太赫兹特殊光束测量、太赫兹表面波观测等,希望该综述能够推动太赫兹脉冲焦平面成像的进一步技术革新和应用拓展。 相似文献
106.
This paper deals with modeling of the phenomenon of fretting fatigue in
heterogeneous materials using the multi-scale computational homogenization technique
and finite element analysis (FEA). The heterogeneous material for the specimens consists
of a single hole model (25% void/cell, 16% void/cell and 10% void/cell) and a four-hole
model (25% void/cell). Using a representative volume element (RVE), we try to produce
the equivalent homogenized properties and work on a homogeneous specimen for the
study of fretting fatigue. Next, the fretting fatigue contact problem is performed for 3 new
cases of models that consist of a homogeneous and a heterogeneous part (single hole cell)
in the contact area. The aim is to analyze the normal and shear stresses of these models
and compare them with the results of the corresponding heterogeneous models based on
the Direct Numerical Simulation (DNS) method. Finally, by comparing the
computational time and % deviations, we draw conclusions about the reliability and
effectiveness of the proposed method. 相似文献
107.
Qiang Fu Xuchan Fan Jianghui Sun Hongwei Tan Yan Wang Jin Ouyang Na Na 《Small (Weinheim an der Bergstrasse, Germany)》2020,16(33)
Visualization of Hg(II) and MeHg in their native contexts is significant for examining mercury poisoning, while it is challenging because of indistinguishable fluorescent (FL) signals during FL imaging. Herein, visualizations of mercury methylation and dynamic transformations of Hg(II) and MeHg are achieved in living biological systems. Well distinguishable FL responses (blue emission for Hg(II), yellow emission for MeHg) are obtained by a double‐response FL probe (DPAHB) without any interference. As demonstrated by experimental and computational studies, the distinguishable signals are attributed to selective binding with DPAHB and different inhibition of excited‐state proton transfer. Through control tests for live‐dead markers, mercury methylation is demonstrated to be employed in living biological systems. Therefore, the methylation and dynamic transformations of both ions are monitored in zebrafish by imaging, and these results are confirmed by traditional high‐performance liquid chromatography‐based methods. The methylation of Hg(II) to MeHg, dynamic transformations and final accumulations of both species in zebrafish tissues are visualized successfully. This method is also convenient for fast evaluation of detoxification reagents. This is the first visualization of in vivo mercury methylation and dynamic transformation of both species and is effective for studying pathological processes in their native contexts. 相似文献
108.
Haibo Zhang Guohua Geng Kang Li Cheng Liu Yuqing Hou 《Journal of Modern Optics》2018,65(20):2278-2289
Cone-beam X-ray luminescence computed tomography (CB-XLCT) is an attractive hybrid imaging modality, and it has the potential of monitoring the metabolic processes of nanophosphors-based drugs in vivo. However, the XLCT imaging suffers from a severe ill-posed problem. In this work, a sparse nonconvex Lp (0?p?1) regularization was utilized for the efficient reconstruction for early detection of small tumour in CB-XLCT imaging. Specifically, we transformed the non-convex optimization problem into an iteratively reweighted scheme based on the L1 regularization. Further, an iteratively reweighted split augmented lagrangian shrinkage algorithm (IRW_SALSA-Lp) was proposed to efficiently solve the non-convex Lp (0?p?1) model. We studied eight different non-convex p-values (1/16, 1/8, 1/4, 3/8, 1/2, 5/8, 3/4, 7/8) in both 3D digital mouse experiments and in vivo experiments. The results demonstrate that the proposed non-convex methods outperform L2 and L1 regularization in accurately recovering sparse targets in CB-XLCT. And among all the non-convex p-values, our Lp(1/4?p?1/2) methods give the best performance. 相似文献
109.
This paper presents a novel technique for progressive online integration of uncalibrated image sequences with substantial geometric and/or photometric discrepancies into a single, geometrically and photometrically consistent image. Our approach can handle large sets of images, acquired from a nearly planar or infinitely distant scene at different resolutions in object domain and under variable local or global illumination conditions. It allows for efficient user guidance as its progressive nature provides a valid and consistent reconstruction at any moment during the online refinement process. Our approach avoids global optimization techniques, as commonly used in the field of image refinement, and progressively incorporates new imagery into a dynamically extendable and memory-efficient Laplacian pyramid. Our image registration process includes a coarse homography and a local refinement stage using optical flow. Photometric consistency is achieved by retaining the photometric intensities given in a reference image, while it is being refined. Globally blurred imagery and local geometric inconsistencies due to, e.g. motion are detected and removed prior to image fusion. We demonstrate the quality and robustness of our approach using several image and video sequences, including handheld acquisition with mobile phones and zooming sequences with consumer cameras. 相似文献
110.
Dr. Luca Gobbi Dr. Joël Mercier Dr. Benny Bang-Andersen Dr. Jean-Marie Nicolas Dr. John Reilly Björn Wagner Dr. David Whitehead Dr. Emmanuelle Briard Dr. R. Paul Maguire Dr. Edilio Borroni Dr. Yves P. Auberson 《ChemMedChem》2020,15(7):560-560
Nonspecific binding (NSB) is a key parameter in optimizing PET imaging tracers. We compared the ability to predict NSB of three available methods: LIMBA, rat fu,brain, and CHI(IAM). Even though NSB is often associated with lipophilicity, we observed that logD does not correlate with any of these assays, clearly indicating that lipophilicity, while influencing NSB, is insufficient to predict it. A cross-comparison of the methods showed that all three correlate and are useful predictors of NSB. The three assays, however, rank the molecules slightly differently, illustrating the challenge of comparing molecules within a narrow chemical space. We also noted that CHI(IAM) values more effectively predict VNS, a measure of in vivo NSB in the human brain. CHI(IAM) measurements might be a closer model of the actual physicochemical interaction between PET tracer candidates and cell membranes, and seems to be the method of choice for the optimization of in vivo NSB. 相似文献