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51.
A. S. Blum W. L. Barr W. L. Dexter J. H. Fink R. W. Moir T. P. Wilcox 《Journal of Fusion Energy》1981,1(1):69-86
We describe a design for a 120-keV, 2.3-MW,3He neutral beam injector for use on a D-3He fusion reactor. The constraint that limits operating life when injecting He is its high sputtering rate. The sputtering is partly controlled by using an extra grid to prevent ion flow from the neutralizer duct to the electron suppressor grid, but a tradeoff between beam current and operating life is still required. Hollow grid wires functioning as mercury heat pipes cool the grid and enable steady state operation. Voltage holding and radiation effects on the acceleration grid structure are discussed. We also briefly describe the vacuum system and analyze use of a direct energy converter to recapture energy from unneutralized ions exiting the neutralizer. Of crucial importance to the technical feasibility of the3He-burning reactor are the injector efficiency and cost; these are 53% and $5.5 million, respectively, when power supplies are included.The beam is composed of 91 separate, parallel currents that flow in the gaps between the elements or wires of a grid. Each such flow is referred to as a beamlet. The current densities in Figs. 5, 8, and 9 are values within a beamlet, as measured at the beam-forming grid. They are not values averaged over the entire beam cross-section. 相似文献
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Two generalizations of the Voronoi diagram in two dimensions (E2) are presented in this paper. The first allows impenetrable barriers that the shortest path must go around. The barriers are straight line segments that may be combined into polygons and even mazes. Each region of the diagram delimits a set of points that have not only the same closest existing point, but have the same topology of shortest path. The edges of this diagram, which has linear complexity in the number of input points and barrier lines, may be hyperbolic sections as well as straight lines. The second construction considers the Voronoi diagram on the surface of a convex polyhedron, given a set of fixed source points on it. Each face is partitioned into regions, such that the shortest path to any goal point in a given region from the closest fixed source point travels over the same sequence of faces to the same closest point. 相似文献
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Hua Zhao Michael S Franklin 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2020,95(9):2301-2310
Coal is the most abundant fossil fuel. Direct combustion of low- and medium-rank coals causes alarming environmental impacts. Therefore, it is crucial for coal to undergo pretreatments before its efficient utilization [such as coal to liquid (CTL) processes]. Conventional pretreatment methods suffer from several limitations including the use of volatile organic solvents, environmental hazards, strong reaction conditions (e.g. high temperature and pressure), consumption of large quantities of nonrecoverable chemicals (e.g. bases used in aqueous alkaline digestion), or being only effective for specific coals. On the other hand, coal pretreatment by nonvolatile ionic liquids (ILs) could lead to partial coal dissolution/swelling and structure disruption, which is a critical step before coal liquefaction, hydrogenation, pyrolysis or the inhibition of oxidation/combustion. In addition, ILs are suitable solvents for extracting sulfur compounds from coal, asphaltenes from Direct Coal Liquefaction Residues (DCLR) and phenolic compounds from coal tar. This review will discuss these aspects of coal pretreatments by ILs, and identify how ILs could lead to a cleaner and more efficient utilization of coal resources. © 2020 Society of Chemical Industry 相似文献
56.
Franklin E. Epiepang Xiong Yang Jianbo Li Yingshu Liu Ralph T. Yang 《American Institute of Chemical Engineers》2018,64(2):406-415
The aim of this work was to reduce/minimize Li in Li‐LSX by replacing the 70% Li+ cations in Li‐LSX that are bonded to the interior or inaccessible sites which are not used for adsorption. Thus, mixed‐cation LiCa‐LSX containing minimum lithium were prepared by exchanging small fractions of Li+ into Ca‐LSX, followed by dehydration under mild conditions to avoid migration/equilibration of Li cations. Comparisons of adsorption isotherms of N2/O2 and heats of adsorption for the LiCa‐LSX samples with that for pure‐cation Li‐LSX and Ca‐LSX provided strong evidence that significant amounts of these Li cations indeed remained on the exposed sites (SIII). The mixed‐cation LiCa‐LSX samples were compared against the pure‐cation Ca‐LSX and Li‐LSX based on their performance for oxygen production by PSA, via model simulation. The results showed that the mixed‐cation LiCa‐LSX samples yielded significantly higher O2 product productivities at the same product purity and recovery than their pure‐cation precursor (Ca‐LSX). © 2017 American Institute of Chemical Engineers AIChE J, 64: 406–415, 2018 相似文献
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Front Cover: [Carboxyl‐11C]Labelling of Four High‐Affinity cPLA2α Inhibitors and Their Evaluation as Radioligands in Mice by Positron Emission Tomography (ChemMedChem 2/2018) 下载免费PDF全文
59.
Curing copolymerization kinetics of styrene with maleated castor oil glycerides obtained from biodiesel‐derived crude glycerol 下载免费PDF全文
Kinetics of curing of maleated castor oil glycerides with styrene was studied by differential scanning calorimetry and rheology. The resin was synthesized from biodiesel‐derived crude glycerol. Curing rates were fitted to several empirical models (autocatalytic model, Kamal's model and a model with vitrification). The three models showed a good fitting with experimental data at conversions lower than 0.55 for temperatures ranging from 30 to 50°C. However, the model that includes vitrification showed a better fitting in the entire range of conversions and the same temperatures. At higher temperatures (50–60°C), some deviations were observed for the three models at low and high conversions. Gel times were obtained from rheological studies and the apparent activation energies were calculated thereof. Gel times were 300–2700 s. The values of apparent activation energy obtained for this castor oil‐based copolymer (47.2–52.3 kJ/mol) were within range of commercial unsaturated polyester resins. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41344. 相似文献
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Influence of chain length of diol on the swelling behavior of citric acid based pH sensitive polymeric hydrogels: A green approach 下载免费PDF全文
Synthesis of pH‐sensitive hydrogels of citric acid with varying diol units viz., 1,2 Ethane diol, 1,4 butane diol, and 1,6 hexane diol along with methacrylic acid towards the solventless green approach. The formations of the hydrogels were identified using FTIR spectroscopy. Thermal characterization (thermo gravimetric analysis, differential thermal analysis (DTA), and differential scanning calorimetry) and morphology of the synthesized hydrogels have been investigated. Swelling studies of hydrogels in various pH ranging from 4.0 to 10.0 have been investigated. The results of the swelling studies implied that percentage of swelling comparatively higher at neutral pH (7.4) than at acidic and alkaline pH. The inverse relationship was noticed, where ascending the diol units of hydrogel in swelling equilibrium. The hydrogels with the increasing chain length show a noticeable pH sensitivity and which could be considered as smart hydrogel. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41403. 相似文献