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41.
The quantitative optical measurement of deep sub-wavelength features with sub-nanometer sensitivity addresses the measurement challenge in the semiconductor fabrication process. Optical scatterings from the sidewalls of patterned devices reveal abundant structural and material information. We demonstrated a parametric indirect microscopic imaging (PIMI) technique that enables recovery of the profile of wavelength-scale objects with deep sub-wavelength resolution, based on measuring and filtering the variations of far-field scattering intensities when the illumination was modulated. The finite-difference time-domain (FDTD) numerical simulation was performed, and the experimental results were compared with atomic force microscopic (AFM) images to verify the resolution improvement achieved with PIMI. This work may provide a new approach to exploring the detailed structure and material properties of sidewalls and edges in semiconductor-patterned devices with enhanced contrast and resolution, compared with using the conventional optical microscopy, while retaining its advantage of a wide field of view and relatively low cost.  相似文献   
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Multimedia Tools and Applications - Digital image communication over public networks requires a high level of security to protect picture elements that represent information. Security is an...  相似文献   
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Cognitive load varies the attention level, which has serious consequences in complex dynamic situations. Assessment of uncertainty in cognitive load during multiple object tracking task is necessary, as it is used to improve the cognitive capabilities. The present research work investigates the uncertainty in cognitive load of multiple object tracking task using electroencephalograph (EEG) on 25 football players. A d2 test of neuropsychological measure of attention was employed before starting the experiment. Each player participated in four levels of the task with variation in the cognitive load, which varies in terms of the targets from 2 to 5. Percentage changes in the power spectral density were estimated for the cognitive levels. Results show that the percentage changes were much more in high cognitive load than in low cognitive load. Significant changes (p < 0.05) were observed in level 1 (− 11.07 to 1.91%), level 2 (− 3.13 to − 14.51%), level 3 (− 6.33 to − 19.46%) and level 4 (− 8.10 to − 20.88%). Variation in the EEG data in terms of the combined uncertainty corresponds very well with low to high cognitive loads. The fourth level of the task with high cognitive load has more uncertainty than the low cognitive load levels. The results are useful for assessing the cognitive state of the player, which is valuable for the design of the effective training model.  相似文献   
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Supported iron oxides have been established as an important class of catalyst for high temperature sulfuric acid decomposition. With an objective to elucidate the role of support in modifying the overall catalytic properties of dispersed iron oxide catalysts, a series of supported iron oxide based catalysts, Fe2O3 (15 wt%)/MO2 (M = Zr, Ce, Ti and Si), synthesized by adsorption-equilibrium method, is investigated for sulfuric acid decomposition reaction. The structure of dispersed iron oxide phases largely depended on the nature of the support oxide as revealed by the XRD and Mössbauer studies. α-Fe2O3 is found to be present as a major phase on ZrO2 and CeO2 support while ε-Fe2O3 was the major phase on silica supported iron oxide. On the other hand, presence of mixed oxide Fe2TiO5 was revealed over TiO2 support. Strong dispersed metal oxide-support interactions inhibited the total reduction of the dispersed phase on SiO2 and TiO2 as compared to complete reduction of dispersed iron oxide on CeO2 and ZrO2 supports during temperature programmed reduction upto 1000 °C. The order of catalytic activity at a temperature of ~750 °C is observed as Fe2O3/SiO2 > Fe2TiO5/TiO2 > Fe2O3/ZrO2 > Fe2O3/CeO2, while at higher temperatures of ~900 °C the SO2 yield is found to be comparable for all catalysts. A relationship between the rate of sulfate decomposition and catalytic activity is established through detailed TG-DTA investigations of sulfated catalyst and support. Considerable influence of the support oxide on the composition, structure, redox properties, morphology and catalytic activities of the active iron oxide dispersed phase has been observed. Thus, the support oxides operate as a critical component in the complex supported metal oxide catalysts and these findings might influence the design and development of future high temperature sulfuric acid decomposition catalysts.  相似文献   
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Blending and interesterification of cold‐pressed oil from commercially available niger (Guizotia abyssinica (L.f.) Cass.) seeds was performed to improve its stability. The fatty acid composition of cold‐pressed niger seed oil (NSO) revealed that it contained a huge amount of polyunsaturated linoleic acid (69.2 %). NSO being rich in polyunsaturated fatty acids (PUFA) was susceptible to oxidation and hence was blended with saturated fatty acid (SFA) rich coconut oil (CNO) and monounsaturated fatty acid (MUFA) rich olive–pomace oil (OO) to enhance its stability. CNO contained a total of 91.3 % of SFA, while OO had oleic acid, C18:1 (74.3 %) as MUFA. Two blends of NSO with CNO and OO, i.e. NSO + CNO(B) and NSO + OO(B), were prepared in the ratio of 1:1. The blends were further interesterified using the lipase enzyme from Rhizomucor meihei and interesterified oils, i.e. NSO + CNO(I) and NSO + OO(I), were obtained. The oxidative stability of the oils was evaluated by incubating them at 37 °C and 55 % relative humidity (RH) for a period of 45 days. The peroxide values of NSO + CNO(B), NSO + OO(B), NSO + CNO(I) and NSO + OO(I) showed a reduction by 53.3, 42.6, 65.3 and 55.4 %, respectively, while the conjugated diene values showed a reduction by 75.0, 66.9, 76.7 and 75.3 %, respectively, as compared to NSO during the incubation period. This is probably the first report on the stability improvement of niger seed oil through blending and interesterification.  相似文献   
48.
The night-vision image fusion plays a critical role in detecting targets and obstructions in low light or total darkness, which has great importance for pedestrian recognition, vehicle navigation, surveillance and monitoring applications. The central idea is to fuse low-light visible and infrared imagery into a single output. In this paper, we describe a new fusion framework for spatially registered visual and infrared images. The proposed framework utilizes the properties of fractal dimension and phase congruency in the non-subsampled contourlet transform (NSCT) domain. The proposed framework applies multiscale NSCT on visual and IR images to get low- and high-frequency bands. The varied frequency bands of the transformed images are then fused while exploiting their characteristics. Finally, the inverse NSCT is performed to get the fused image. The performance of the proposed framework is validated by extensive experiments on different scene imaginary, where the definite advantages are demonstrated subjectively and objectively.  相似文献   
49.
Oxidation of cyclohexane has been carried out using molecular oxygen over cobalt molybdenum oxide (CoMoO4) catalysts in solvent free conditions. The catalysts were prepared using citrate method with three different molar ratios of Co:Mo, 1:1, 1:2, and 2:1 along with individual oxides for comparative studies. While all the catalysts showed significant activity and selectivity, CoMoO4 with 1:1 ratio showed the best performance compared to the others with a conversion of 7.38%, with selectivity to cyclohexanol and cyclohexanone (KA oil) of 94.3%, in 1 h. The performance of the catalyst, has been studied as a function of oxygen pressure, reaction temperature, and catalyst loading. It was observed that the catalyst deactivates during the course of the reaction. The reasons for deactivation and methods for restoring the activity have been studied. A kinetic model is presented that captures the complex kinetics and matches well with the experimental data. © 2016 American Institute of Chemical Engineers AIChE J, 62: 4384–4402, 2016  相似文献   
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