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Electrochemical copolymerization of diphenylamine (DPA) with o‐chloroaniline (OCA) was performed in aqueous 4M sulfuric acid using the pulse potentiostatic method (PPSM). By employing the tunable parameters in PPSM, polymeric films were deposited under different conditions. Cyclic voltammetry was used for evaluating the characteristics of the deposited polymeric films. A suitable growth equation for the deposition of polymer, relating the charge associated for the film deposition and the pulse parameters in PPSM, was deduced. Various surface parameters are evaluated. The formation of copolymer during PPSM deposition was revealed through critical analysis of the results. The characteristic differences between the individual homopolymers, poly(diphenylamine) and poly(o‐chloroaniline) and the copolymer, poly(diphenylamine‐co‐o‐chloroaniline), were brought out. The copolymer was also synthesized through a chemical method and characterized through infrared and ultraviolet‐visible spectroscopic analysis. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 389–397, 2003  相似文献   
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Topics in Catalysis - CO2 reforming of methanol for producing hydrogen was experimentally carried out in a fixed-bed reactor on 10%Ni/SiO2. The 10%Ni/SiO2 was completely reduced during H2...  相似文献   
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A systematic analysis of several vacuum swing adsorption (VSA) cycles with Zeochem zeolite 13X as the adsorbent to capture CO2 from dry, flue gas containing 15% CO2 in N2 is reported. Full optimization of the analyzed VSA cycles using genetic algorithm has been performed to obtain purity‐recovery and energy‐productivity Pareto fronts. These cycles are assessed for their ability to produce high‐purity CO2 at high recovery. Configurations satisfying 90% purity‐recovery constraints are ranked according to their energy‐productivity Pareto fronts. It is shown that a 4‐step VSA cycle with light product pressurization gives the minimum energy penalty of 131 kWh/tonne CO2 captured at a productivity of 0.57 mol CO2/m3 adsorbent/s. The minimum energy consumption required to achieve 95 and 97% purities, both at 90% recoveries, are 154 and 186 kWh/tonne CO2 captured, respectively. For the proposed cycle, it is shown that significant increase in productivity can be achieved with a marginal increase in energy consumption. © 2013 American Institute of Chemical Engineers AIChE J, 59: 4735–4748, 2013  相似文献   
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Highly transparent Aluminum oxynitride (AlON) body has been produced using aqueous slip casting technique. High‐purity alumina and AlN were used as raw materials for the synthesis of single‐phase AlON powder. As‐synthesized AlON powder was surface modified to enable the AlON powders resistant to hydrolysis in water during aqueous slip casting. High solid loaded aqueous AlON slip was prepared for casting followed by drying and sintering to produce transparent AlON. Phase formation and stability was characterized by XRD, pH, and viscosity measurements. AlON powders before and after surface treatments were characterized. Sintered transparent AlON samples were characterized for their mechanical, microstructural, and optical properties. Sintered and polished AlON produced in this study has shown inline transparency up to 80% between 0.22 and 6 μm wavelength region.  相似文献   
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Polymer blend electrolytes comprising of poly(vinyl acetate), poly(vinylidene fluoride-co-hexafluoropropylene), LiClO4, and EC-based plasticizer combinations (EC + PC, EC + GBL, EC + DMP, EC + DBP, EC + DEC) are prepared by solvent casting technique. Ionic conductivities of the electrolytes are determined by ac impedance studies in the temperature range 303–363 K. Among the various combinations of plasticizers, EC + PC added complex exhibits maximum ionic conductivity of the order of 10−4 S cm−1 and the temperature-dependent ionic conductivity plots seem to obey the VTF relation. The structural and complex formations of the prepared samples have been confirmed by X-ray diffraction analysis. DSC technique is used to study the thermal behaviour. The surface images of the sample having maximum ionic conductivity are analyzed with the help of SEM and AFM techniques.  相似文献   
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Polypyrrole (PPy) and Polypyrrole‐ZnO (PPy‐ZnO) nanocomposites were electrodeposited on mild steel and its corrosion protection ability was studied by Tafel and Impedance techniques in 3.5% NaCl solution. Pure Polypyrrole film was not found to protect the mild steel perfectly but the coating with nano‐sized ZnO (PPy‐ZnO) has dramatically increased the corrosion resistance of mild steel. Electrochemical Impedance Spectroscopy (EIS) measurements indicated that the coating resistance (Rcoat) and corrosion resistance (Rcorr) values for the PPy‐ZnO nanocomposite coating was much higher than that of pure PPy coated electrode. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   
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Modification of polymeric membrane materials by incorporation of hydrophilicity results in membranes with low fouling behavior and high flux. Hence, Polysulfone was functionalized by sulfonation and ultrafiltration membranes were prepared based on sulfonated polysulfone and cellulose acetate in various blend compositions. Polyethyleneglycol 600 was employed as a nonsolvent additive in various concentrations to the casting solution to improve the ultrafiltration performance of the resulting membranes. The total polymer concentration, cellulose acetate, and sulfonated polysulfone polymer blend composition, additive concentration, and its compatibility with polymer blends were optimized. The membranes prepared were characterized in terms of compaction, pure water flux, membrane resistance, and water content. The compaction takes place within 3–4 h for all the membranes. The pure water flux is determined largely by the composition of sulfonated polysulfone and concentration of additive. Membrane resistance is inversely proportional to pure water flux, and water content is proportional to pure water flux for all the membranes. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1749–1761, 2002  相似文献   
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Miscanthus fibers reinforced biodegradable poly(butylene adipate‐co‐terephthalate) (PBAT) matrix‐based biocomposites were produced by melt processing. The performances of the produced PBAT/miscanthus composites were evaluated by means of mechanical, thermal, and morphological analysis. Compared to neat PBAT, the flexural strength, flexural modulus, storage modulus, and tensile modulus were increased after the addition of miscanthus fibers into the PBAT matrix. These improvements were attributed to the strong reinforcing effect of miscanthus fibers. The polarity difference between the PBAT matrix and the miscanthus fibers leads to weak interaction between the phases in the resulting composites. This weak interaction was evidenced in the impact strength and tensile strength of the uncompatibilized PBAT composites. Therefore, maleic anhydride (MAH)‐grafted PBAT was prepared as compatibilizer by melt free radical grafting reaction. The MAH grafting on the PBAT was confirmed by Fourier transform infrared spectroscopy. The interfacial bonding between the miscanthus fibers and PBAT was improved with the addition of 5 wt % of MAH‐grafted PBAT (MAH‐g‐PBAT) compatibilizer. The improved interaction between the PBAT and the miscanthus fiber was corroborated with mechanical and morphological properties. The compatibilized PBAT composite with 40 wt % miscanthus fibers exhibited an average heat deflection temperature of 81 °C, notched Izod impact strength of 184 J/m, tensile strength of 19.4 MPa, and flexural strength of 22 MPa. From the scanning electron microscopy analysis, better interaction between the components can be observed in the compatibilized composites, which contribute to enhanced mechanical properties. Overall, the addition of miscanthus fibers into a PBAT matrix showed a significant benefit in terms of economic competitiveness and functional performances. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45448.  相似文献   
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