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41.
    
Conventional solid-state power amplifier (SSPA) design approach isolates radio frequency (RF) design from communication theory. In this paper, a unified SSPA design approach is proposed, which optimizes SSPA parameters (bias voltage and input RF signal power) to minimize total DC power consumption while satisfying received SNR constraint specified by the link budget. The effect of SSPA nonlinearity is quantified by the error vector magnitude measured at its output and the corresponding received SNR degradation is analyzed. Using the quantitative metrics for received SNR, it is possible to evaluate highly nonlinear SSPA classes such as Class-B or deep-Class AB, which are normally not considered in conventional SSPA design approach to be used in satellite communication applications.  相似文献   
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One of the most prominent energy storage technologies which are under continuous development, especially for mobile applications, is the Li‐ion batteries due to their superior gravimetric and volumetric energy density. However, limited cycle life of Li‐ion batteries inhibits their extended use in stationary energy storage applications. To enable wider market penetration of Li‐ion batteries, detailed understanding of the degradation mechanisms is required. A typical Li‐ion battery comprised of an active material, binder, separator, current collector, and electrolyte, and the interaction between these components plays a critical role in successful operation of such batteries. Degradation of Li‐ion batteries can have both chemical and mechanical origins and manifests itself by capacity loss, power fading or both. Mechanical degradation mechanisms are associated with the volume changes and stress generated during repetitive intercalation of Li ions into the active material, whereas chemical degradation mechanisms are associated with the parasitic side reactions such as solid electrolyte interphase formation, electrolyte decomposition/reduction and active material dissolution. In this study, the main degradation mechanisms in Li‐ion batteries are reviewed. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   
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ABSTRACT

Wind turbine control is an important task to make the electricity generation secure in terms of energy demand and machine safety. It also yields to control the desired power level and optimized energy because of the assignment of turbine speed. The contactless piezoelectric wind energy harvester (CPWEH) used in this study has three piezoelectric layers located around the shaft with 120 degrees apart and they are buckled by the magnetic force without any physical contact. The superiority of this device is to generate energy for low wind speeds such as 1.5 m/s. However, for high speeds, high total harmonic distortions (THDs) govern the waveforms, thus controlling the turbine speed becomes necessary for optimizing the output power. Encouraged by this, a small low inertia dc generator is coupled with the wind turbine, and the generator terminals are connected to a resistor through a power switch to generate a braking torque that opposes to wind speed direction. By controlling the switch properly, turbine speed is ensured to remain within a certain band, which accordingly prevents the turbine from rotating very fast at damaging wind speeds. Several experiments are performed on the developed CPWEH with/without the presented control scheme which prove the existence of promising performance of our proposal.  相似文献   
46.
    
The use of flame retardants (FRs) to improve the flame retardancy but also having good insulation and mechanical properties of rigid polyurethane foam (RPUF) has become significant due to the increasing demand in both the industry and academia. In the present study, a series of RPUF composites containing expandable graphite (EG), ammonium pentaborate (APB) octahydrate, and their binary blends were prepared with one-shot and free-rise methods. The effects of FRs on the FR and physical-mechanical properties of RPUFs were investigated. The results show that both EG and APB could improve the flame retardancy of RPUFs and reduced the smoke production. The FR effect of EG was better than APB and more importantly, synergistic effect was found between EG and APB. The best results were obtained by the foam in the composition of 15E and 5A. The cone calorimeter test results showed that the peak heat release rate (pHRR) and total smoke release (THR) of 15E/5A foam were lower than the foams of 20E and 20A. The pHRR and THR values of 15E/5A foam decreased about 57.5% and 42.8% compared to the neat RPUF, respectively. Total smoke production (m2) also reduced about 77.0% by 20E and 83.6% by 15E/5A foams. Thermogravimetric analysis indicates that the char residue of 15E/5A foam increased to 39.5%, which provided better flame retardancy. The foam composites have high compressive strength (105-150 kPa) and low thermal conductivity values (19.9-21.3 mW/mK). While the thermal conductivity of 15E/5A foam increased by 0.5%, its compressive strength increased by 6.1%.  相似文献   
47.
    
Calcium oxalate (CaOx) is the major phase in kidney stones and the primary calcium storage medium in plants. CaOx can form crystals with different lattice types, water contents, and crystal structures. However, the conditions and mechanisms leading to nucleation of particular CaOx crystals are unclear. Here, liquid-cell transmission electron microscopy and atomistic molecular dynamics simulations are used to study in situ CaOx nucleation at different conditions. The observations reveal that rhombohedral CaOx monohydrate (COM) can nucleate via a classical pathway, while square COM can nucleate via a non-classical multiphase pathway. Citrate, a kidney stone inhibitor, increases the solubility of calcium by forming calcium-citrate complexes and blocks oxalate ions from approaching calcium. The presence of multiple hydrated ionic species draws additional water molecules into nucleating CaOx dihydrate crystals. These findings reveal that by controlling the nucleation pathways one can determine the macroscale crystal structure, hydration state, and morphology of CaOx.  相似文献   
48.
    
Electrolyte additives have been widely used to address critical issues in current metal (ion) battery technologies. While their functions as solid electrolyte interface forming agents are reasonably well-understood, their interactions in the liquid electrolyte environment remain rather elusive. This lack of knowledge represents a significant bottleneck that hinders the development of improved electrolyte systems. Here, the key role of additives in promoting cation (e.g., Li+) desolvation is unraveled. In particular, nitrate anions (NO3) are found to incorporate into the solvation shells, change the local environment of cations (e.g., Li+) as well as their coordination in the electrolytes. The combination of these effects leads to effective Li+ desolvation and enhanced battery performance. Remarkably, the inexpensive NaNO3 can successfully substitute the widely used LiNO3 offering superior long-term stability of Li+ (de-)intercalation at the graphite anode and suppressed polysulfide shuttle effect at the sulfur cathode, while enhancing the performance of lithium–sulfur full batteries (initial capacity of 1153 mAh g−1 at 0.25C) with Coulombic efficiency of ≈100% over 300 cycles. This work provides important new insights into the unexplored effects of additives and paves the way to developing improved electrolytes for electrochemical energy storage applications.  相似文献   
49.
    
In this study, novel polyethersulfone (PES) and poly(trimethoxysilyl) propyl methacrylate (PMPS) containing hybrid materials were prepared. PES was functionalized with trimethoxysilane groups by UV‐induced grafting reaction. PMPS was synthesized by atom transfer radical polymerization. In the followed process, the functionalized PES mixed with different amount of PMPS, thermally treated to promote sol–gel crosslinking process to prepare the PES‐based hybrid materials. The trimethoxysilane grafted PES chains are covalently bonded with the well‐defined trimethoxysilane groups of PMPS. The chemical structure of the prepared PES and PMPS is confirmed by Fourier transform infrared analysis. The morphology of the hybrids was investigated by scanning electron microscopy. The results of thermogravimetric analysis show that the thermal stability of the hybrid materials was significantly affected with the addition of PMPS. POLYM. ENG. SCI., 58:1346–1352, 2018. © 2017 Society of Plastics Engineers  相似文献   
50.
    
The purpose of this paper is to introduce a novel UV‐cured interpenetrating polymer networked phase change materials (IPN‐PCMs), on which no article has been found in the so far published research. Maleated castor oil (MCO) was synthesized via maleinization reaction of castor oil with maleic anhydride. Organic–inorganic hybrid interpenetrating polymer networked (IPN) materials containing both cationic and radical sections and IPN‐PCMs containing tetradecanol, hexadecanol, and octadecanol were prepared. The chemical structure of MCO and organic–inorganic hybrid IPN‐PCMs were determined by using Fourier Transform Infrared Spectroscopy (FT‐IR). Differential scanning calorimetry (DSC) was used for examining the phase‐change behaviors of the materials. Thermal stability was investigated by thermogravimetric analysis (TGA). Moreover, the surface formation of the specimen was investigated by scanning electron microscopy (SEM). In conclusion, our study proved that because of their high latent heat storage scope and high thermal stability, the obtained organic–inorganic hybrid IPN‐PCMs could be used as thermal energy storage materials. POLYM. ENG. SCI., 58:870–875, 2018. © 2017 Society of Plastics Engineers  相似文献   
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