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41.
Sn-20.0 wt%In (Sn-20.0In) alloy is a promising base material in Pb-free solders for low-temperature applications. Zn is often used as an additive to Pb-free solders to reduce the extent of undercooling during reflow. Cu is the most commonly used substrate in electronics industry. Interfacial stability at Sn–In–Zn/Cu joints is crucial to reliability of electronic products. In this study, interfacial reactions between Sn-20.0 wt%In-x wt%Zn (Sn-20.0In-xZn) solders and Cu where x = 0.5, 0.7, 1.0, 2.0, 3.0, and 5.0 at 150, 230, and 260 °C were experimentally examined. It is found that the reaction phase formation and interfacial morphologies are strongly influenced by Zn concentrations. The reaction phases evolve from the Cu6Sn5 phase, CuZn and Cu5Zn8 phase, to Cu5Zn8 phase with higher Zn doping in the solders. The Cu5Zn8 phase acted as a diffusion barrier and suppressed the growth of the Cu6Sn5 phase. The results indicate that 2.0 wt%Zn addition resulted in the gentlest reactions during both soldering and solid-state ageing in Sn-20.0In-xZn/Cu couples.  相似文献   
42.
Selective activation technique was used to define a semi-insulating current-blocking layer underneath the p-pad of InGaN-GaN multiple-quantum-well light-emitting diodes (LEDs). The output power of the LEDs at 20 mA was increased 10% because less current was injected underneath the opaque p-pad.  相似文献   
43.
The dose-dependent pharmacokinetics of caffeic acid (CA) were studied in rabbits. Three different doses (5, 10, and 25 mg kg-1) were administered intravenously to six rabbits each. The concentration-time profiles for CA could be fitted by a two-compartment model for each dose. The results showed that total-body clearance and elimination rate constant from the central compartment (k10) after a 5 mg kg-1 dose were greater than those after the other two doses. Furthermore, the terminal elimination half-life (beta half-life) and mean residence time (MRT) after a 5 mg kg-1 dose were less than after the other doses. The AUC value increased linearly with dose within the range of 10-25 mg kg-1. Most of the unchanged caffeic acid was excreted in the urine within 2 h. The percentage of unchanged caffeic acid excreted in the urine was 63.4, 60.0, and 55.4% after doses of 5, 10, and 25 mg kg-1, respectively, which was not significantly different. However, significant differences in the renal clearances and renal excretion rate constants were observed with a 5 mg kg-1 dose compared to the other doses. On the other hand, nonrenal clearances and nonrenal excretion rate constants showed no dose-related differences. The differences observed in total-body clearance, k10, beta half-life, and MRT between a 5 mg kg-1 dose and the other doses can be explained on the basis of the differences in renal clearance and renal excretion rate constants.  相似文献   
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45.
The influence of particle morphology on the accuracy of nanoparticle size distributions measured by the engine exhaust particle sizer spectrometer (EEPS, TSI Model 3090) was studied using the scanning mobility particle sizer (SMPS, TSI Model 3936) as a reference. The EEPS shows higher total number concentrations with the maximum relative difference up to 67 % and smaller number median mobility diameters for polydisperse silver nanoparticles generated in the laboratory. To provide a quantitative explanation of the difference, generated polydisperse nanoparticles were classified as monodisperse particles with the initial equivalent mobility diameter (d m1) and sintered in the second furnace at different temperatures (room temperature to 600 °C), to change their morphologies for the comparison tests. Without sintering (room temperature), results show that the measured mobility diameter (d m2) of the EEPS is smaller than that measured by the SMPS when d m1 is larger than 30 nm and the difference increases as d m1 is increased from 30 to 300 nm. But the difference decreases as the morphology of particles is changed from branched chain agglomerates to spheres for d m1 less than 80 nm and the sintering temperature higher than 200 °C. Theoretical analysis shows that the mean charge per agglomerates is more than that of spheres resulting in overestimation of the electrical mobility and underestimation of the d m2 by the EEPS.  相似文献   
46.
A novel active personal nanoparticle sampler (PENS), which enables the collection of both respirable particulate mass (RPM) and nanoparticles (NPs) simultaneously, was developed to meet the critical demand for personal sampling of engineered nanomaterials (ENMs) in workplaces. The PENS consists of a respirable cyclone and a micro-orifice impactor with the cutoff aerodynamic diameter (d(pa50)) of 4 μm and 100 nm, respectively. The micro-orifice impactor has a fixed micro-orifice plate (137 nozzles of 55 μm in the inner diameter) and a rotating, silicone oil-coated Teflon filter substrate at 1 rpm to achieve a uniform particle deposition and avoid solid particle bounce. A final filter is used after the impactor to collect the NPs. Calibration results show that the d(pa50) of the respirable cyclone and the micro-orifice impactor are 3.92 ± 0.22 μm and 101.4 ± 0.1 nm, respectively. The d(pa50) at the loaded micro-Al(2)O(3) mass of 0.36-3.18 mg is shifted to 102.9-101.2 nm, respectively, while it is shifted to 98.9-97.8 nm at the loaded nano-TiO(2) mass of 0.92-1.78 mg, respectively. That is, the shift of d(pa50) due to solid particle loading is small if the PENS is not overloaded. Both NPs and RPM concentrations were found to agree well with those of the IOSH respirable cyclone and MOUDI. By using the present PENS, the collected samples can be further analyzed for chemical species concentrations besides gravimetric analysis to determine the actual exposure concentrations of ENMs in both RPM and NPs fractions in workplaces, which are often influenced by the background or incident pollution sources.  相似文献   
47.
In this study we used Suzuki cross-coupling to synthesize three new donor/acceptor copolymers—PFTBO, PAFTBO, and PCTBO—featuring soluble alkoxy-modified 2,1,3-benzooxadiazole (BO) moieties as acceptor units and electron-rich building blocks—dialkyl fluorene (F), alkylidene fluorene (AF), and carbazole (C), respectively—as donor units. These polymers, which we characterized using gel permeation chromatography, thermogravimetric analysis, NMR spectroscopy, UV–Vis absorption spectroscopy, and electrochemical cyclic voltammetry, exhibited good solubility, low-lying energy levels for their highest occupied molecular orbitals, excellent thermal stability, and air stability. Using these polymers, we fabricated bulk-heterojunction solar cell devices having the structure indium tin oxide/poly(3,4-ethylenedioxythiophene):polystyrenesulfonate/polymer:[6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) (1:1, w/w)/Ca/Al. Under AM 1.5G illumination (100 mW cm?2), the solar cell incorporating PFTBO exhibited a high value of Voc of 1.04 V and that based on PCTBO provided a power conversion efficiency of 4.1% without the need for any post treatment.  相似文献   
48.
The inverse boundary optimization problem, governed by the Helmholtz equation, is analyzed by the Trefftz method (TM) and the exponentially convergent scalar homotopy algorithm (ECSHA). In the inverse boundary optimization problem, the position for part of boundary with given boundary condition is unknown, and the position for the rest of boundary with additionally specified boundary conditions is given. Therefore, it is very difficult to handle the boundary optimization problem by any numerical scheme. In order to stably solve the boundary optimization problem, the TM, one kind of boundary-type meshless methods, is adopted in this study, since it can avoid the generation of mesh grid and numerical integration. In the boundary optimization problem governed by the Helmholtz equation, the numerical solution of TM is expressed as linear combination of the T-complete functions. When this problem is considered by TM, a system of nonlinear algebraic equations will be formed and solved by ECSHA which will converge exponentially. The evolutionary process of ECSHA can acquire the unknown coefficients in TM and the spatial position of the unknown boundary simultaneously. Some numerical examples will be provided to demonstrate the ability and accuracy of the proposed scheme. Besides, the stability of the proposed meshless method will be validated by adding some noise into the boundary conditions.  相似文献   
49.
The aim of this study was to examine the influence of carbon content on the microstructures and corrosion characteristics. The results showed that the hypereutectic microstructure comprised primary (Cr,Fe)7C3 carbides and the eutectic colonies [γ-Fe + (Cr,Fe)7C3]. The amounts of primary (Cr,Fe)7C3 carbides increased from 33.81 to 86.14% when carbon content increased from 3.73 to 4.85 wt%. The corrosion resistance of the hypereutectic alloy with 4.85 wt% C was about 20 times higher than that with 3.73 wt% C. The galvanic corrosion occurred in all claddings due to difference of corrosion potential between primary carbide and austenite. The dense distribution of primary carbides could retard the austenitic matrix from selective corrosion. The austenite dissolved the Fe2+ ions and formed a Cr2O3 film under 3.5% NaCl aqueous solution.  相似文献   
50.
The current study used flux core arc welding to produce a series of hypereutectic Fe-Cr-C claddings with various carbon content. Depending on the carbon content, this research produced hypereutectic microstructures of γ-Fe + (Cr,Fe)7C3 carbides. As the carbon content of a cladding increased from 3.73 to 4.85 wt.%, the surface fractions of carbides increased from 33.8% to 86.1%. The morphology of primary (Cr,Fe)7C3 carbides also transited from a blade-like to a rod-like shape. With regard to wear performance, the relationship between wear resistance and hardness (H) is non-linear. However, the mean free path (λ) of primary (Cr,Fe)7C3 carbides must be considered. Wear resistance is proportional to H/λ. The primary carbides can prevent the eutectic colonies from selective abrasion. The rod-like (Cr,Fe)7C3 carbides also provide much better wear resistance because rod-like carbides have a greater hardness. After an abrasive wear process, abrasive particles cause plastic plows when the cladding has lower surface fractions of carbides. The fracture of primary carbides leads into the craters where it occurs in the worn cladding surface with higher surface fractions of carbides.  相似文献   
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