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41.
《International Journal of Hydrogen Energy》2021,46(74):37039-37048
Herein, poly (phenylene) oxide (PPO)-based cross-linked anion exchange membranes (AEMs) with flexible, long-chain, bis-imidazolium cation cross-linkers are designed and synthesized. Although the cross-linked membranes possess high ion exchange capacity (IEC) values of up to 3.51–3.94 meq g−1, they have a low swelling degree and good mechanical strength because of their cross-linked structure. Though the membranes with the longest flexible bis-imidazolium cation cross-linker (BMImH-PPO) possess the lowest IEC among these PPO-based AEMs, they show the highest conductivity (24.10 mS cm−1 at 20 °C) and highest power density (325.7 mW cm−2 at 60 °C) because of the wide hydrophilic/hydrophobic microphase separation in the membranes that promote the construction of ion transport channels, as confirmed by atom force microscope (AFM) images and the small angle X-ray scattering (SAXS) analyses. Furthermore, the BMImH-PPO samples exhibit good chemical stability (10% and 6% decrease in IEC and conductivity, respectively, in 2 M KOH at 80 °C for 480 h, and a 22% decrease in weight in Fenton's reagent at 60 °C for 120 h), making such cross-linked AEMs potentially applicable in alkaline anion exchange membrane fuel cells. 相似文献
42.
Hang Shi Qiuyang Yu Guoliang Liu Xiaohong Hu 《International Journal of Hydrogen Energy》2021,46(33):17097-17105
Transition metal phosphides (TMPs) have been considered as cheap alternatives of precious metal platinum for electrochemical hydrogen evolution reaction (HER). In the past decades, many reports have indicated that the engineering of heterointerfaces between different components could efficiently enhance the activity of HER catalysts. Here, we report a facile method to construct Ni12P5–Ni2P heterostructure by using a low temperature phosphorization strategy. The obtained Ni12P5–Ni2P heterostructure shows high activity toward HER with an overpotential value of 166 mV at 10 mA cm?2 and a Tafel slope of 60 mV dec?1 in 0.5 M H2SO4. Compared with pure Ni2P and Ni12P5, the Ni12P5–Ni2P heterostructure has more active sites and faster HER kinetics due to the presence of the interfaces between Ni12P5 and Ni2P. Furthermore, we used the obtained Ni12P5–Ni2P as cathodic catalyst and IrO2/Ti as anodic material to set up a proton exchange membrane (PEM) electrolyzer which shows good stability after 120 h continuous constant current electrolysis at 200 mA cm?2. This work demonstrates the positive effect of heterostructure for HER catalysts and provides a feasible strategy for constructing earth-abundant electrocatalysts. 相似文献
43.
Sirshendu Guha 《American Institute of Chemical Engineers》2022,68(3):e17505
In continuation to my previous work (Guha S. AIChE J. 2013;59(4):1390-1399), in this work, effects of ionic migration are evaluated for disk region of a rotating ring disk electrode system by numerically solving complex differential equations, developed for mass transfer along with kinetic complication in presence of ionic migration under limiting current condition. The system for simulation is 0.01 M Fe2(SO4)3 solution with H2SO4 as supporting electrolyte. Simulation cases are presence and absence of ionic migration with kinetic complication (oxidation of Fe2+ to Fe3+ under O2 pressure). Results show that concentration boundary layer thickness of reactant Fe3+ reduces appreciably and steady-state disk current reduces substantially in presence of migration. Simulated steady-state disk current in absence of migration case agrees well with published data. Results indicate higher Fe2+ concentration in presence of migration and thereby higher rate of oxidation of Fe2+ to Fe3+ at all rate constant values. 相似文献
44.
Farida khan Naeem A Israf Ud Din T. Saeed Mshari A. Alotaibi Abdulrahman I. Alharthi Asad Habib Tabassum Malik 《Ceramics International》2021,47(4):4749-4757
In the present study, hexagonal boron nitride (h-BN) was synthesized from boric acid and melamine by thermal annealing method in a nitrogen atmosphere. The pure h-BN was used as an efficient sorbent for the uptake of Cd2+ ions from the solution phase. The kinetics and sorption studies of metal ions onto the h-BN were carried out in batch adsorption experiments at different temperature, time, pH, sorbent dosage, and concentration of metal ions. The optimum pH for the removal of the Cd2+ ions was found to be pH 7. The effect of temperature showed that the process of Cd2+ sorption remained endothermic in the range of 298 K–328 K. The Lagergren's first and Ho's second kinetic models were tested to interpret the adsorption kinetic data, however the present data was explained well by Ho's model for kinetics. The thermodynamic perameters ΔG, ΔS and ΔH were determined using the available adsorption data at different temperatures. The physicochemical properties of the synthesized product were also characterized before and after adsorption by different analytical techniques like FT-IR, TGA, XRD and Point of Zero Charge (PZC). The morphology of the surface was analyzed with the help of Scanning Electron Microscopy. The h-BN proved to be an efficient adsorbent for the uptake of the Cd2+ ions from aqueous media. 相似文献
45.
Wang Hay Kan Chenxi Wei Dongchang Chen Tao Bo Bao‐Tian Wang Yan Zhang Yangchao Tian Jun‐Sik Lee Yijin Liu Guoying Chen 《Advanced functional materials》2019,29(17)
Lithium‐rich disordered rock‐salt oxides have attracted great interest owing to their promising performance as Li‐ion battery cathodes. While experimental and theoretical efforts are critical in advancing this class of materials, a fundamental understanding of key property changes upon Li extraction is largely missing. In the present study, single‐crystal synthesis of a new disordered rock‐salt cathode material, Li1.3Ta0.3Mn0.4O2 (LTMO), and its use as a model compound to investigate Li concentration–driven evolution of local cationic ordering, charge compensation, and chemical distribution are reported. Through the combined use of 2D and 3D X‐ray nanotomography, it is shown that Li removal accompanied by oxygen oxidation is correlated with the development of morphological defects such as particle cracking. Chemical heterogeneity, quantified by subparticle level distribution of Mn valence state, is minimal during Mn redox, which drastically increases upon the formation of cracks during oxygen redox. Density functional theory and bond valence sum mismatch calculations reveal the presence of local short‐range ordering in the pristine oxide, which gradually disappears along with the extraction of Li. The study suggests that with cycling the transformation into true cation–disordered state can be expected, which likely impacts the voltage profile and obtainable energy density of the oxide cathodes. 相似文献
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47.
Portfolio selection is a key issue in the business world and financial fields. This article presents a new decision making method of portfolio optimization (PO) issues in different risk measures by using new evolutionary computing method and cardinality constrains which is mentioned as hybrid meta-heuristic algorithms. Based on mean–variance (MV) Method by Markowitz we collected three risk levels; mean absolute deviation (MAD), semi variance (SV) and variance with skewness (VWS). The developed algorithms are Electromagnetism-like algorithm (EM), particle swarm optimization (PSO), genetic algorithm (GA), genetic network programming (GNP) and simulated annealing (SA). Also a diversification mechanism strategy is implemented and hybridized with the developed algorithms to increase the diversity and overcome local optimality. The sustainability of this proposed model is verified by 50 factories on the Iranian stock exchange. Finally, experimental results of proposed algorithms with cardinality constraint are compared with each other by four effective metrics in which the algorithms performance for achieving the optimal solution discussed. In addition, we have done the analysis of variance technique to confirm the validity and accurately analyze of the results which the success of this method was proved. 相似文献
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