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排序方式: 共有197条查询结果,搜索用时 15 毫秒
191.
检测自由曲面时精确定位方法的研究 总被引:5,自引:1,他引:5
针对用三坐标测量机对自由曲面轮廓进行测量时由于工件找正时的定位误差引起的测量误差,提出了一种将实际测量数据点与工件的CAD模型理论数据点优化匹配的算法。使用该算法可有效地消除最终测量结果中由于定位误差引起的系统误差 相似文献
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193.
Chen Davidovich Matthew Belousoff Itai Wekselman Tal Shapira Miri Krupkin Ella Zimmerman Anat Bashan Ada Yonath 《Israel journal of chemistry》2010,50(1):29-35
The ribosome is a ribozyme whose active site, the peptidyl transferase center (PTC), is situated within a highly conserved universal symmetrical region that connects all ribosomal functional centers involved in amino acid polymerization. The linkage between this elaborate architecture and A-site tRNA position revealed that the A- to P-site passage of the tRNA 3′ terminus during protein synthesis is performed by a rotary motion, synchronized with the overall tRNA/mRNA sideways movement, and guided by the PTC. This rotary motion leads to suitable stereochemistry for peptide bond formation as well as for substrate-mediated catalysis. Analysis of the substrate binding modes to ribosomes led to the hypothesis that the ancient ribosome produced single peptide bonds and non-coded chains, potentially in a similar manner to the modern PTC. Later in evolution, a mechanism, enabling some type of decoding genetic control triggered the emergence of the small ribosomal subunit or part of it. This seems to be the result of the appearance of reaction products that could have evolved after polypeptides capable of enzymatic function were generated sporadically, while an ancient stable RNA fold was converted into an old version of a tRNA molecule. Since in the contemporary ribosome, the symmetry relates only to the backbone fold and nucleotide orientations but not nucleotide sequences, it emphasizes the superiority of functional requirement over sequence conservation, and indicates that the PTC may have evolved by gene fusion or gene duplication. 相似文献
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196.
Ada A. Barbosa Ramon V. S. de Aquino Marina G. Silva Welenilton J. do Nascimento Júnior Marta M. M. B. Duarte Renato F. Dantas Otidene R. S. da Rocha 《加拿大化工杂志》2020,98(5):1124-1138
This study presents a new aluminium mesh made out of soda can rings as a support for titanium dioxide (TiO2) in the degradation of the synthetic dyes Bordeaux Red (BR) and Tartrazine (TT). Three pre-treatments including calcination and acidification steps were investigated in order to select the most efficient immobilization procedure for photocatalysis application. Raw and titania-aluminum meshes were characterized by scanning electron microscopy, x-ray diffraction, diffuse reflectance, and Fourier transform infrared spectroscopy. The material presented itself as a suitable alternative in the immobilization of titania for wastewater treatment. Preliminary tests selected H2O2/TiO2(suspension) oxidation systems under natural sunlight and germicidal lamps (UVC) exhibiting 97.2% and 99.5% of degradation in 180 minutes, respectively. Immobilized TiO2 systems reached high degradation rates (>99%) after 180 minutes in both UVC and solar light-based processes. An experimental planning study was carried out for the processes in order to find the best operational conditions and pseudo-first-order model fit well the removal data (discolouration rates of in the order of 0.0274 and 0.0145 min−1 for UVC and solar light systems, respectively). Parameters such as TOC, COD, and turbidity, revealed a great improvement in the environmental quality of the water after the treatment and acute toxicity bioassays demonstrated a significant decrease in toxicity for both systems after the treatments. The TiO2-meshes demonstrated high performance in the removal after five cycles of operation. Therefore, the new immobilization procedure demonstrated that the TiO2-aluminum mesh is a feasible option for wastewater treatment and photocatalysis. 相似文献
197.
Mingfei Xiao Boseok Kang Seon Baek Lee Luís M. A. Perdigão Alex Luci Daniel A. Warr Satyaprasad P. Senanayak Mark Nikolka Martin Statz Yutian Wu Aditya Sadhanala Sam Schott Remington Carey Qijing Wang Mijung Lee Chaewon Kim Ada Onwubiko Cameron Jellett Hailiang Liao Wan Yue Kilwon Cho Giovanni Costantini Iain McCulloch Henning Sirringhaus 《Advanced materials (Deerfield Beach, Fla.)》2020,32(23):2000063
Precise control of the microstructure in organic semiconductors (OSCs) is essential for developing high-performance organic electronic devices. Here, a comprehensive charge transport characterization of two recently reported rigid-rod conjugated polymers that do not contain single bonds in the main chain is reported. It is demonstrated that the molecular design of the polymer makes it possible to achieve an extended linear backbone structure, which can be directly visualized by high-resolution scanning tunneling microscopy (STM). The rigid structure of the polymers allows the formation of thin films with uniaxially aligned polymer chains by using a simple one-step solution-shear/bar coating technique. These aligned films show a high optical anisotropy with a dichroic ratio of up to a factor of 6. Transport measurements performed using top-gate bottom-contact field-effect transistors exhibit a high saturation electron mobility of 0.2 cm2 V−1 s−1 along the alignment direction, which is more than six times higher than the value reported in the previous work. This work demonstrates that this new class of polymers is able to achieve mobility values comparable to state-of-the-art n-type polymers and identifies an effective processing strategy for this class of rigid-rod polymer system to optimize their charge transport properties. 相似文献