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101.
《International Journal of Hydrogen Energy》2019,44(3):1967-1972
The Formic Acid Electro-oxidation (FAEO) on Pt/Au Nanoparticles (PtAu NP) supported on Hierarchical Porous Carbon (HPC), was studied by cyclic voltammetry and chronoamperometry. The supported HPC-Pt nanoparticles were surface modified by Au spontaneous deposits. The morphological and compositional characterization was performed by Scanning Electron Microscopy (SEM) coupled with Electron Dispersive Spectroscopy (EDS). A significant increase of the current densities for FAEO in the potential region 0.1–0.75 VRHE was observed on HPC-PtAu catalysts. The comparison with HPC-Pt electrodes results show that Au atoms presence on Pt nanoparticles is a key factor to improve the catalysts performance. Based on our results, a clear change in FAEO mechanism on HPC-PtAu catalysts with respect to HPC-Pt was evidenced. 相似文献
102.
103.
《International Journal of Hydrogen Energy》2019,44(36):20336-20344
The interconnecred PtIr alloy nanowires were uniformly deposited on carbon cloth via One-step wet chemistry method, which diameter is averaged to be 5 nm with a length of 50–200 nm. The carbon cloth supported PtIr nanowire assembly (PtIr NA/CC) shows a larger electrochemical active surface area (ECSA) due to its 3D nanostructure and a high CO-resistance as a result from the synergistic effect of PtIr alloy. The PtIr NA/CC exhibits an extremely high mass activity and a reliable long-term stability toward methanol oxidation reaction (MOR). The superior catalytic performance on MOR can match and even surpass those best Pt-based nanowires reported recently in the literature. 相似文献
104.
油脂酯交换催化剂研究进展 总被引:1,自引:1,他引:1
酯交换是油脂改性主要方法之一,应用催化剂可降低反应温度,加快反应速度。该文主要对油脂酯交换催化剂研究进展进行综述。 相似文献
105.
SAPO-34,SAPO-5/34 based catalysts doped with Cu,Ce as active components were synthesized via a one-pot hydrothermal method by using different amounts of additive(a-cellulose),and their catalytic activities were measured for selective catalytic reduction(SCR) of NO with NH3.The synthesized Cu-Ce co-doped products switch from cubic SAPO-34,to flower-like aggregated SAPO-5/34,hybrid crystal SAPO-5/34,and finally to spherical aggregated SAPO-34 with the increase of α-cellulose amount.The Cu-Ce co-doped SAPO-5/34 hybrid crystal structure catalysts with 0.75 mol ratios of C/P(Cu-Ce/SP-0.75)exhibit excellent NH3-SCR activity with higher than 90% NO_x conversion in the temperature range of 180-450℃,at WHSV of 20000 mL/(g·h).Furthermore,the catalyst displays outstanding sulfur resistance and NO_X conversion maintains above 90% at 200-450℃ after adding 100 ppm of SO_2.The characteristic results suggest that the high deNO_X performance of Cu-Ce/SP-0.75 is due to the enhanced accessibility,abundant activity species,excellent redox property and high adsorptive and activated capacity for NH3. 相似文献
106.
Eranezhuth Wasan Awin Timon E. Günther Rameshwori Loukrakpam Stefan Schafföner Christina Roth Günter Motz 《International Journal of Applied Ceramic Technology》2023,20(1):59-69
The development of efficient and durable catalysts is critical for the commercialization of fuel cells, as the catalysts’ durability and reactivity dictate their ultimate lifetime and activity. In this work, amorphous silicon-based ceramics (Si–C–N and Si–Al–C–N) and TiN@Si–Al–C–N nanocomposites were developed using a precursor derived ceramics approach. In TiN@Si–Al–C–N nanocomposites, TiN nanocrystals (with sizes in the range of 5–12 nm) were effectively anchored on an amorphous Si–Al–C–N support. The nanocomposites were found to be mesoporous in nature and exhibited a surface area as high as 132 m2/g. The average pore size of the nanocomposites was found to increase with an increase in the pyrolysis temperature, and a subsequent graphitization of free carbon was observed as revealed from the Raman spectra. The ceramics were investigated for electrocatalytic activity toward the oxygen reduction reaction using the rotating disk electrode method. The TiN@Si–Al–C–N nanocomposites showed an onset potential of 0.7 V versus reversible hydrogen electrode for oxygen reduction, which seems to indicate a 4-electron pathway at the pyrolysis temperature of 1000°C in contrast to a 2-electron pathway exhibited by the nanocomposites pyrolyzed at 750°C via the Koutecky–Levich plot. 相似文献
107.
Activity of monolithic perovskite catalysts in oxidation of selected hydrocarbons and oxy-derivatives, oxidized individually and in two-component mixtures, as well as the reaction selectivity were investigated. One bulk perovskite (LaMn2O3) catalyst and two catalysts based on LaMn2O3 with addition of silver (25 at.%) coated on cordierite support were prepared for the study. The efficiency of oxy-derivatives oxidation was higher than that of hydrocarbon oxidation, but some by-products (first of all aldehydes) were detected in the flue gases. Addition of silver to the active phase improved catalyst activity and selectivity to CO2 and water. The “mixture effect” on catalyst activity and selectivity depended on composition of the reaction mixture and the catalyst used. The presence of oxy-derivative in the reaction mixture inhibited oxidation of hydrocarbons. Toluene inhibited the process of oxy-derivatives conversion and increased the concentration of incomplete oxidation products. 相似文献
108.
Different methods to prepare supported metal nanoparticles of uniform size are discussed. (i) Supported ruthenium particles were generated from Ru and Ru-Fe bimetallic molecular metal carbonyl cluster precursors (MCC). (ii) Gold nanoparticle formation in the supercage of Y zeolite was studied on Au/NaY, Au/HY and Au-Fe/HY system. (iii) Palladium nanoparticles were grown in liquid phase then deposited on an SiO2 support or they were grown on the support surface in a solid-liquid interfacial layer. The particle size control was more efficient in the latter two cases than in the preparation starting from MCC. 相似文献
109.
110.
Arnaud Barbier Guy-Antonin Martin Pilar Ramirez de la Piscina Narcis Homs 《Applied Catalysis A: General》2001,210(1-2):75-81
The hydrogenation of carbon monoxide over Co/SiO2 catalysts obtained by reduction of precursors prepared by the reaction of dicobaltoctacarbonyl with silica gives rise to a mixture of alcohols and hydrocarbons. The chain growth probability for hydrocarbon synthesis is similar to that observed over conventional catalysts prepared by the ammonia method (=0.74) with a comparable metal dispersion (metal particle size 4 nm). Alcohol formation yields a smaller chain growth probability (=0.42). Magnetic measurements have shown that in the latter catalyst, small cobalt clusters (1 nm) are likely to be present together with the cobalt particles (4 nm), this observation reconciles apparently conflicting results from the literature. It has been speculated that alcohol formation might be related to the presence of these clusters according to a concerted mechanism. Furthermore, the observation of large amounts of acetates by temperature-programmed hydrogenation, not detected in hydrocarbon selective catalysts, suggests that they may play a role in ethanol synthesis. 相似文献