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351.
An e.s.r. study of γ-irradiated isotactic (i-) and atactic (a-) polypropylene (PP) was carried out. Both the 17 line (or 9 line) spectrum for i-PP and the 6 line spectrum for a-PP are attributed to the tertiary carbon radical, CH2C(CH3)CH2. The difference in the hyperfine structure between the spectrum of i-PP and that of a-PP can be explained by different radical conformations owing to the stereoregularity. Hyperfine coupling and the radical conformation for the tertiary carbon radical in i- and a-PP were determined from the cos2 ? rule. It is shown that the δ methylene proton as well as the β methylene proton contribute to the slight anisotropy in the stretched sample. The spectral change from 9 lines to 17 lines with elevation of temperature, observed at low temperature in i-PP, could be explained by the hindered oscillation of the β methylene proton.  相似文献   
352.
The effect of crystallization on the structure and morphology of maleic anhydride grafted polypropylene (PP‐MA)/clay (montmorillonite) nanocomposites (PPCNs) is presented. Wide‐angle X‐ray diffraction (WAXD) measurements of PPCNs crystallized at different temperatures show that the extent of intercalation increases with the crystallization temperature. The enhancement of intercalation occurs with lower clay content PPCNs, and maximum intercalation takes place for 4 wt% clay content. The mechanism of intercalation has been proposed through crystallization. Excess γ‐form of the crystallite of PP‐MA appears in presence of clay, possibly because of the confinement of the polymer chain between the clay particles. WAXD data also reveals that d‐spacing increases gradually with clay content. The decrease of spherulitic size is observed with increasing clay content, which indicates that clay particles act as nucleating agents. Lamellar textures have been explored by using small angle X‐ray scattering (SAXS) and transmission electron microscopy (TEM), which exhibit that both the lamellar thickness and long period of the PPCNs are higher than those of PP‐MA.  相似文献   
353.
The measurement of rheological properties of any polymeric material under molten state is crucial to gain fundamental understanding of the processability of that material. In the case of polymer/layered silicate nanocomposites, the measurements of rheological properties are not only important to understand the knowledge of the processability of these materials, but is also helpful to find out the strength of polymer‐layered silicate interactions and the structure‐property relationship in nanocomposites. This is because rheological behaviors are strongly influenced by their nanoscale structure and interfacial characteristics. In order to get this knowledge in the case of polylactide/montmorillonite nanocomposites, we have studied melt rheological properties of these materials in detail. On the basis of rheological data, we have conducted foam processing of pure polylactide and one representative nanocomposite by a newly developed pressure cell technique using carbon dioxide as a physical‐blowing agent.

The time variation of the elongational viscosity of one of the intercalated polylactide/montmorillonite nanocomposites.  相似文献   

354.
Summary: For the reference system of PPS‐based nanocomposites, we investigated the intercalation behavior of DFS molecules into nano galleries based on OMLFs consisting of different types of intercalants and nanofillers with different surface charge densities. The smaller initial interlayer opening led to the larger interlayer expansion, regardless of the miscibility between the intercalant and DFS. We examined the preparation of PPS‐based nanocomposites with and/or without shear processing at 300 °C. The finer dispersion of OMLFs in the nanocomposite was observed when using OMLF having small initial interlayer opening. The delamination of the stacked nanofillers was governed by the initial interlayer opening, whereas the uniform dispersion of the nanofillers was affected by the shear.

Plot of initial interlayer opening versus Δ opening for various OMLFs intercalated with DFS.  相似文献   

355.
The constraints on the PID gains, which are derived from the H norm performance index by discretization of the frequency, are convex or concave depending on frequencies. This problem is a non‐convex problem, and a new method of approximating these constraints as adequate linear inequalities is proposed. Then, the optimal solution can be efficiently and successfully searched for by applying linear programming iteratively. This method is compared with methods based on barrier function and linear matrix inequality. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   
356.
More than 20 years have passed since the introduction of advanced water treatment with ozonation and granular activated carbon in the Hanshin Water Supply Authority. Significant improvements have been achieved in eliminating taste and odor compounds in water and in suppressing the formation of disinfection by-products. Regarding the bromate ion, we have managed to suppress its formation by keeping the residual ozone concentration and pH low.  相似文献   
357.
To understand the enzymatic degradation behavior of crosslinked polylactide (PLA), the preparation and enzymatic degradation of both thermoplastic (linear) and crosslinked PLAs that have pore structures with different dimensions were carried out. The porous structures of the linear PLA samples were of micro and nanoporous nature, and prepared by batch foaming with supercritical CO2 and compared with the porous structures of crosslinked PLA (Lait-X) created by the salt leaching method. The surface and cross-sectional morphologies of the porous structures were investigated by using scanning electron microscopy. The morphological analysis of porous Lait-X showed a rapid loss of physical features within 120 h of exposure to proteinase-K enzymatic degradation at 37 °C. Due to the higher affinity for water, enhanced enzymatic activity as compared to the linear PLA porous structures in the micro and nanoporous range was observed.  相似文献   
358.
Diamond-like carbon (DLC) films have been attractive materials because of their excellent mechanical properties such as high hardness, low friction coefficient, high wear resistance and more. In order to spread the application of the DLC coatings for polymer materials, it is necessary to make the temperature go down during the coating process.Our group has been studying DLC coatings on several materials with bipolar pulse type PBII (plasma based ion implantation) systems, which consist of positive and negative (or bipolar) pulse generators and a timing controller. Recently we have introduced a new bipolar pulse generator, whose slew-rate is several times larger than that of previous generators, and a controller which can make a very short pulse less than 1 μs. Using the pulse generator and controller, we have tried to make Si incorporated DLC (Si-DLC) coatings on fluoro rubber, which is widely used in many industries, at low temperature.Using the new pulse generator and controller, we can make very short width positive pulse of about 1 μs, and reduce the temperature during Si-DLC coating to about 30 K. The lower temperature makes fewer folds on the sample surface. By using optical indentation microscope system, Meyer hardness (HM) of uncoated and Si-DLC coated fluoro rubber was obtained and the value of HM for Si-DLC coated rubber is about 1.4 times larger than that of uncoated rubber. Coefficient of friction of Si-DLC coated rubber was 0.2 to 0.25 and drastically decreased from 1.3 to 1.9 of uncoated rubber. Wear of uncoated fluoro rubber is apparent, however, wear of Si-DLC coated rubber cannot be observed, except for the creep effect of fluoro rubber substrate. The counter SUJ2 ball surfaces also showed almost no wear. Si-DLC coating can make the tribological property of fluoro rubber to low friction and less wear. Si-DLC coatings are very useful in many applications.  相似文献   
359.
360.
The fabrication of tissue engineering scaffolds based on the polymerization of crosslinked polylactide using leaching and batch foaming to generate well‐controlled and interconnected biodegradable polymer scaffolds is reported. The scaffold fabrication parameters are studied in relation to the interpore connectivity, pore morphology, and structural stability of the crosslinked PLA scaffold. In vitro cell culture and in vitro degradation are used to analyze the biocompatibility and biodegradability of the scaffolds. The new crosslinked PLA thermoset scaffolds are highly suitable for bone tissue engineering applications due to their complex internal architecture, thermal stability, and biocompatibility.

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