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91.
The influence of different magnesium (Mg) weight percentages (1, 2.5, 5, 7.5 and 10) over silver (3 wt%) impregnated alumina (SA) catalyst was investigated for the reduction of NO by C3H6. Mg doped SA catalysts were prepared by conventional impregnation method and characterized by XRD, BET-SA, ICP-MS, XPS, SEM, UV-DRS, H2-TPR and O2-TPD. The existence of MgO and MgAl2O4 phases on Mg doped SA catalysts were observed from XRD and XPS analyses. Existence of high percentage MgAl2O4 phase on 5% Mg doped SA catalyst (Mg (5) SA) enhances the dispersion and stabilization of silver phases (Ag2O). Mg (5) SA catalyst shows a 51% of high selectivity (NO to N2) in presence of SO2 (80 ppm) at low temperatures (350 °C) and maintained high selectivity’s with a wide temperature window (350–500 °C). An optimal high surface availability of Ag0 and Ag+ species were observed from XPS analysis over Mg (5) SA catalyst. H2-TPR analysis shows high temperature reduction peak over Mg (5) SA compared to SA catalyst. XPS analysis confirms the high percent availability of MgAl2O4 species over Mg (5) SA catalyst. DRIFTS study reveals the molecular evidences for the evolution of enolic species during NO reduction over the highly active Mg (5) SA catalyst at low temperatures. It also confirms further transformation of enolic species into –NCO species with NO + O2 and finally into N2 and CO2.  相似文献   
92.
Kinetics of swelling and sorption behavior of copolymers (based on linseed oil, styrene, divinylbenzene, and acrylic acid via cationic and thermal polymerization) is studied in tetrahydrofuran (THF) at different temperatures. The values of n in the transport equation are found to be below 0.4, showing non‐Fickian or pseudo‐Fickian transport in the polymers. The dependence of diffusion coefficient on the composition and temperature has also been studied for the linseed oil‐based polymers. The diffusion coefficient in cationic samples decreases with an increase in the oil contents in the samples. In case of thermal samples, the diffusion coefficient first increases up to 30% oil contents and then decreases. The diffusion coefficient decreases with an increase in temperature for all of the linseed oil polymer samples. The sorption coefficient increases with an increase in the oil contents for all samples. The crosslink density (calculated from the THF swelling) ranges from 20.16 to 92.34 × 106 mol/cm3 for cationic samples and 20.62 to 86.01 × 106 mol/cm3 for thermal samples. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009  相似文献   
93.
The solvent‐resistance properties of the montmorillonite‐filled conjugated linseed oil‐based nanocomposites are studied in tetrahydrofuran through equilibrium swelling method at different temperatures. The values of “n” in solvent transport equation are found to be below “0.5,” showing the non‐Fickian diffusion in the polymer. The dependence of the diffusion coefficient on the composition, percentage of clay, and temperature has been studied for nanocomposite samples. The diffusion coefficient increases with an increase in the clay contents and temperature. The crosslink density of the nanocomposites ranges from 101.07 to 237.46 × 106 mol/cm3. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009  相似文献   
94.
Ultra-fine grained copper with a large amount of nano-scale twin boundaries has high mechanical strength and maintains normal electrical conductivity. The combination of these properties may lead to promising applications in future Si microelectronic technology, especially as interconnect material for air-gap and free-standing copper technologies. Based on first principles calculations of total energy and in-situ stress measurements, high stress followed by stress relaxation during the Cu film deposition seems to have contributed to nanotwin formation. Nanoindentation studies have shown a larger hardness for copper with a higher nanotwin density. The effect of Cu nanotwin boundaries on grain growth was investigated by scanning electron microscopy (SEM), electron backscatter diffraction (EBSD) and transmission electron microscopy (TEM). The presence of a high density of nanotwin boundaries may improve the reliability of Cu interconnects.  相似文献   
95.
Pb(Zr,Ti)O3 (PZT) thin films deposited on insulating ZrO2 buffered silicon wafer are intended to be employed for in-plane polarized piezoelectric MEMS devices. Multi-target reactive sputtering system for large area deposition of in-situ crystallized PZT thin films and the ZrO2 buffer layer has been employed. The interface analysis of multilayer structures by high resolution transmission microscope, X-ray diffraction, optical refraction, and absorption spectra studies has been presented. At a substrate temperature of 520°C and excess lead deposition condition, the formation of a PZT superstructure has been revealed. The substrate temperature of 580°C leads to the crystallization of PZT directly into a single phase perovskite crystal structure. A pronounced Urbach behavior in our PZT thin films has been observed by optical absorption studies. The surface roughness of PZT films deposited on a ZrO2 buffer layer is much higher than that on conducting platinized silicon wafer.  相似文献   
96.
Utilization of industrial waste as substrates for the rhamnolipid synthesis by Pseudomonas aeruginosa is a worthy alternative for conventionally used vegetable oils and fatty acids to reduce the production cost of rhamnolipid. Sunflower acid oil (SAO), a by-product of the oil industry, contains 70% 18:0 fatty acid, with oleic acid as a major component. In this scope, production and analysis of rhamnolipid was successfully demonstrated using SAO as a new substrate. Pseudomonas aeruginosa produced rhamnolipid (a glycolipid biosurfactant) at a maximum concentration of 4.9 g L−1 with 60 g L−1 of SAO in the medium. Structural properties of rhamnolipid biosurfactant are confirmed using thin layer chromatography (TLC), high performance liquid chromatography (HPLC), and fourier transformed infrared spectroscopy (FTIR) analysis. Further surface-active properties of the crude rhamnolipid were evaluated by measuring surface tension and emulsification properties. The synthesized rhamnolipid reduced the surface tension of water to 30.12 mN m−1 and interfacial tension (against heptane) to 0.52 mN m−1. Moreover, rhamnolipid shows the highest emulsification index (above 80%) for vegetable oils. This study confirms the use of SAO as a potential substrate for rhamnolipid production. The synthesized rhamnolipid was incorporated in liquid detergent formulation along with alpha olefin sulfonate (AOS) and sodium lauryl ether sulfate (SLES). The performance properties including foaming and cleaning efficiency of liquid detergent were compared.  相似文献   
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Poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) (PEO–PPO–PEO) triblock copolymer (Pluronic F127) was modified by introducing poly(N‐isopropylacrylamide) (PNIPAM) at both the PEO ends, and the pentablock copolymer (PNIPAM41–F127–PNIPAM41, PN41) so prepared was characterized using gel permeation chromatography and 1H NMR spectroscopy. The degree of polymerization of NIPAM blocks at the two ends was 41. The solution behaviour and microstructure of PN41 aggregates in water were examined using UV–visible spectroscopy, micro‐differential scanning calorimetry and small‐angle neutron scattering (SANS) and compared with F127. Two lower critical solution temperatures (LCSTs) were observed for the pentablock copolymer, corresponding to PPO and PNIPAM blocks, respectively. The adsorption of PN41 on thiol‐grafted hydrophobic gold surfaces at various temperatures was investigated using a quartz crystal microbalance. It was found that the adsorption behaviour and mechanism of PN41 were mainly determined by the interactions of the pentablock copolymers with different chain conformations in dilute aqueous solutions at various temperatures. SANS measurements were used to determine the temperature‐dependent structural evolution of polymer micelles in aqueous solution. A NOESY study revealed that above the LSCT of PNIPAM, the interaction of PPO and PNIPAM protons increases and the distance between PPO and PNIPAM decreases. © 2019 Society of Chemical Industry  相似文献   
100.
The photocatalytic hydrogen generation is a novel, eco-friendly and favourable method for production of green and clean energy using light energy. In this direction, we report low-temperature ionothermal method for the preparation of TiO2 nanoparticles (NPs) using methoxy ethyl methyl imidazolium tris (pentafluoroethyl) trifluoro phosphate (MOEMINtf2) as an ionic liquid (IL) at 120°C for 1 day. The synthesized nanomaterials were examined using different spectrochemical methods like UV-DRS, XRD, FT-IR, TEM, BET and TGA-DTA techniques. The mixed phase TiO2 is obtained with 81.7% of anatase and 18.3% of rutile phase by the XRD studies, and average crystallite size is found to be ∼7 nm. The stretching of Ti-O bond (∼555 cm−1) and few other bands related to ionic liquid were confirmed by FTIR spectrum. The band gap energy was observed to be ∼3.38 eV by UV-DRS analysis. TEM images reveal spherical shape with an average particles size of about 10 nm. Photocatalytic H2 generation was carried out using TiO2 NPs and observed the generation of 553 μmol h−1 g−1 via water splitting reaction. Furthermore, the prepared TiO2 NPs employed for the photocatalytic degradation of methylene blue dye (84.54%), and photoluminescence studies confirms the obtained material can be used in optoelectronic applications with green emission.  相似文献   
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