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991.
992.
Connor J. Appel Jaroslav Kloužek Nikhil Jani Seung Min Lee Derek R. Dixon Pavel Hrma Richard Pokorný Michael J. Schweiger Albert A. Kruger 《Journal of the American Ceramic Society》2019,102(12):7594-7605
Reductants, such as sucrose (C12H22O11), are added to nuclear waste melter feeds containing high fractions of nitrates and nitrites to reduce excessive foaming during feed-to-glass conversion, decrease sulfate segregation, and increase technetium retention. The effect of sucrose on foaming and melting reactions during the conversion was examined using the feed volume expansion test, thermogravimetric analysis, evolved gas analysis, x-ray diffraction, and scanning electron microscopy with energy dispersive x-ray spectrometry. Different amounts of sucrose were added to vary the carbon to nitrogen (C/N) ratio in the melter feed. As the C/N ratio increased, the extent of foaming decreased, and the N2/NO ratio increased in the evolved gas. Significant foam suppression, rapid gas release at approximately 250°C, and reduction in transition metal oxides were observed at C/N > 1.1. 相似文献
993.
The movement of hydrophobic particles in a rising froth column is investigated. Gadolinium particles are hydrophobized and floated by means of small air bubbles. The generated froth is investigated by neutron imaging. Particles are identified by correlating the resulting radiographs with an artificial template of a typical particle and subsequent scanning for local maxima. The movement of the particles in the froth was analyzed for different froth stabilities, which resulted from various concentrations of the frother sodium oleate. Decreasing froth stability leads to lower superficial vertical particle velocity and to higher horizontal diffusion of particles due to bubble rupture. 相似文献
994.
Pavel Topka Vladimír Hejtmnek Gerardo J. F. Cruz Olga olcov Karel Soukup 《化学工程与技术》2019,42(4):851-858
Activated carbon prepared from cocoa pod husk, which is an abundant agricultural waste, was employed as a green support for palladium oxidation catalysts. Systematic characterization of the support and palladium catalysts by atomic emission spectroscopy, N2 and CO2 physisorption measurements, X‐ray powder diffraction, infrared spectroscopy, electron microscopy, temperature‐programmed reduction by hydrogen, and temperature‐programmed desorption of NH3 and CO2 allowed detailed monitoring of their characteristics. Subsequently, the catalytic performance and selectivity in the oxidation of ethanol as a model volatile organic compound (VOC) was studied and linked to physicochemical properties of the catalysts. 相似文献
995.
Kristina N. Iost Vadim A. Borisov Victor L. Temerev Yury V. Surovikin Polina E. Pavluchenko Mikhail V. Trenikhin Aleksey B. Arbuzov Dmitry A. Shlyapin Pavel G. Tsyrulnikov Aleksey A. Vedyagin 《International Journal of Hydrogen Energy》2018,43(37):17656-17663
The resistance of the Pd/C samples towards hydrogenation of the carbon support was studied in the temperature-programmed and isothermal regimes. Carbonaceous graphite-like material Sibunit was used as a carbon support. Pristine Sibunit was additionally graphitized via high temperature treatment (1900 °C) in an inert atmosphere. Both initial and graphitized supports were subjected to oxidative treatment in order to increase the amount of surface functional oxygen-containing groups. Palladium (1 wt%) was supported using an aqueous solution of H2PdCl4. All the samples were characterized by a low-temperature adsorption of nitrogen, transmission electron microscopy, and Raman spectroscopy. The graphitization procedure was found to decrease significantly the specific surface area of the support, while the oxidative treatment affects this parameter negligibly. Testing the Pd-containing samples in a hydrogen flow revealed the following order in accordance with amount of methane released: Pd/iSib » Pd/iSib-ox > Pd/gSib > Pd/gSib-ox. 相似文献
996.
Direct isosurface volume rendering is the most prominent modern method for medical data visualization. It is based on finding intersection points between the rays corresponding to pixels on the screen and isosurface. This article describes a two-pass algorithm for accelerating the method on the graphic processing unit (GPU). On the first pass, the intersections with the isosurface are found only for a small number of rays, which is done by rendering into a lower-resolution texture. On the second pass, the obtained information is used to efficiently calculate the intersection points of all the other. The number of rays to use during the first pass is determined by using an adaptive algorithm, which runs on the central processing unit (CPU) in parallel with the second pass of the rendering. The proposed approach allows to significantly speed up isosurface visualization without quality loss. Experiments show acceleration up to 10 times in comparison with a common ray casting method implemented on GPU. To the authors’ knowledge, this is the fastest approach for ray casting which does not require any preprocessing and could be run on common GPUs. 相似文献
997.
998.
999.
Pavel Levin J��r��mie Lefebvre Theodore J. Perkins 《Journal of the Royal Society Interface》2012,9(77):3411-3425
Many biomolecular systems depend on orderly sequences of chemical transformations or reactions. Yet, the dynamics of single molecules or small-copy-number molecular systems are significantly stochastic. Here, we propose state sequence analysis—a new approach for predicting or visualizing the behaviour of stochastic molecular systems by computing maximum probability state sequences, based on initial conditions or boundary conditions. We demonstrate this approach by analysing the acquisition of drug-resistance mutations in the human immunodeficiency virus genome, which depends on rare events occurring on the time scale of years, and the stochastic opening and closing behaviour of a single sodium ion channel, which occurs on the time scale of milliseconds. In both cases, we find that our approach yields novel insights into the stochastic dynamical behaviour of these systems, including insights that are not correctly reproduced in standard time-discretization approaches to trajectory analysis. 相似文献
1000.
Johannes M. Scheiger Shuai Li Marius Brehm Andreas Bartschat Patrick Theato Pavel A. Levkin 《Advanced functional materials》2021,31(49):2105681
Organogels (hydrophobic polymer gels) are soft materials based on polymeric networks swollen in organic solvents. They are hydrophobic and possess a high content of solvent and low surface adhesion, rendering them interesting in applications such as encapsulants, drug delivery, actuators, slippery surfaces (self-cleaning, anti-waxing, anti-bacterial), or for oil-water separation. To design functional organogels, strategies to control their shape and surface structure are required. Herein, the inherent UV photodegradability of poly(methacrylate) organogels is reported. No additional photosensitizers are required to efficiently degrade organogels (d ≈ 1 mm) on the minute scale. A low UV absorbance and a high swelling ability of the solvent infusing the organogel are found to be beneficial for fast photodegradation, which is expected to be transferrable to other gel photochemistry. Organogel arrays, films, and structured organogel surfaces are prepared, and their extraction ability and slippery properties are examined. Films of inherently photodegradable organogels on copper circuit boards serve as the first ever positive gel photoresist. Spatially photodegraded organogel films protect or reveal copper surfaces against an etchant (FeCl3 aq.). 相似文献