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101.
The phase behavior of novel, binary organic‐inorganic hybrids consisting of an ultra‐low Tg tin‐based phosphate glass (Pglass) and polystyrene (PS) was investigated. Dynamic mechanical analysis (DMA) revealed that the glass transition peaks of the PS changed slightly with Pglass volume fraction, leading to a broad peak at the phase inversion point. The phase inversion and degree of phase continuity of the hybrid were studied through solvent extraction, optical/scanning electron microscopy, and dynamic rheology. The Jordhamo and Utracki viscosity ratio models provided reliable estimates of the inversion point. Torque rheometry revealed a trend toward linear additivity within the temperature range 200°C–230°C. Small‐angle neutron scattering experiments gave further evidence of the hybrid phase incompatibility. The results of this study point to a promising new class of blend materials with the potential to present a unique combination of properties impossible to achieve with classical polymer blends. Polym. Eng. Sci. 44:1692–1701, 2004. © 2004 Society of Plastics Engineers.  相似文献   
102.
We describe a new method for focusing and concentrating a stream of moving micron-sized aerosol particles in air. The focusing and concentrating process is carried out by the combined drag force and optical force that is generated by a double-layer co-axial nozzle and a focused doughnut-shaped hollow laser beam, respectively. This method should supply a new tool for aerosol science and related research.

Copyright © 2018 American Association for Aerosol Research  相似文献   

103.
A novel class of organic‐inorganic polymer hybrids was developed by melt‐blending up to 50 (v/v) % [about 83 (w/w) %] tin‐based polyphosphate glass (Pglass) and low‐density polyethylene (LDPE) in conventional plastics processing equipment. The liquid‐ and solid‐state rheology of the polymer hybrids was studied under oscillatory shear flow and deformation to understand the behavior of these materials and to accelerate efforts to melt process the Pglass with organic polymers. All the materials were found to be linearly viscoelastic in the range of temperature and frequencies examined and their viscoelastic functions increased with increasing Pglass concentration. The Pglass significantly enhanced the shear‐thinning characteristics of the Pglass‐LDPE hybrid, indicating the presence of nonlinear chemical and physical interactions between the hybrid components. Morphological examination of the materials by scanning electron microscopy revealed interesting evolution of microstructure of the Pglass phase from droplets (or round beads) to elongated and interpenetrating network structures as the glass concentration was increased in the Pglass‐LDPE hybrids. Melt viscosities of the materials were well described by a simple power‐law equation and a Maxwellian (Hookean) model with three relaxation times. Time‐temperature superpositioning (TTS) of the complex viscosity versus frequency data was excellent at 170°C < T < 220°C and the temperature dependencies of the shift factors conformed excellently well to predictions from an Arrhenius‐type relation, enabling calculation of the flow‐activation energies (25–285 kj/mol) for the materials. The beneficial function of the Pglass in the hybrid system was significantly enhanced by pre‐treating the glass with coupling agents prior to incorporating them into the Pglass‐LDPE hybrids.  相似文献   
104.
The dielectric behavior of some polar aromatics dissolved in nonpolar unoriented and stretched linear low‐density polyethylene was investigated within the temperature region between 150 and 350 K. The measurements were carried out in the frequency range 1 kHz to 10 MHz. The maximum temperatures and the half widths of the loss tangent peaks depend upon the shape and the polar structure of guest molecules. Stretching the samples induced a shift of the loss tangent to higher temperatures, decreased the height, and increased the width of tan δ peak. The activation energy is also influenced by the type of guest molecules and orientation of polymer matrix. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1278–1282, 2001  相似文献   
105.
Oxidoreductases are attractive biocatalysts that convert achiral substrates into products of higher value, but they are also for the most part dependent on nicotinamide cofactors. Recently, biomimetic nicotinamide derivatives have received attention as less costly alternatives to natural cofactors. However, recycling of biomimetics is still challenging because there are only limited opportunities. Here, we have characterized various biomimetic cofactors with regard to stability and redox potentials to find the best alternative to natural cofactors. Further, the cofactor spectrum of NADH oxidase from Lactobacillus pentosus (LpNox) could be expanded, and the enzymatic activity was also compared to activities with different small‐molecule catalysts. As a result, we succeeded in identifying several strategies for regeneration of oxidized biomimetics.  相似文献   
106.
The atomic and electronic structures of inversion domain boundaries in Mn‐Al dual‐doped ZnO (Zn0.89Mn0.1Al0.01O) have been investigated. Using atomic‐resolution scanning transmission electron microscopy, a head‐to‐head c‐axis configuration and cation stacking sequence of αβαβ|γ|αβαβ along the c‐axis were observed at the basal‐plane inversion domain boundary. Energy‐dispersive X‐ray spectroscopy and electron energy‐loss spectroscopy revealed significant localization of Mn and minor localization of Al at the basal‐plane inversion domain boundary. Based on experimental findings, a Mn‐doped basal‐plane inversion domain boundary slab model was constructed and refined by first principles calculations. The model is in agreement with atomic‐resolution images. The local electronic density of states of the slab model basal‐plane inversion domain boundary shows a hybridization of the Mn d and O p states within the valence band and localized Mn d states in the conduction band. The thermoelectric properties of Zn0.99?xMnxAl0.01O ceramics have been reported in a previous work. In this work, the effects of inversion domain boundaries on the thermoelectric properties are discussed. In comparison to Zn0.99?xMnxAl0.01O ceramics with x≤0.05, inversion domain boundaries in Zn0.89Mn0.1Al0.01O caused thermal and electrical conductivity reduction due to interface scattering of phonons and electrons. The Seebeck coefficient increased, suggesting electron filtering at inversion domain boundaries.  相似文献   
107.
We conducted a detailed evaluation of a method for measuring the mass concentrations and size distributions of black carbon (BC) particles in rainwater and snow. The method uses an ultrasonic nebulizer (USN) and a single particle soot photometer (SP2). The USN disperses sample water into micron-size droplets at a constant rate and then dries them to release BC particles into the air. The masses of individual BC particles are measured by the SP2, using the laser-induced incandescence technique. The loss of BC particles during the extraction from liquid water to air depends on their sizes. We determined the size-dependent extraction efficiency using polystyrene latex (PSL) spheres with 12 different diameters between 107 and 1025 nm. The PSL concentrations in water were measured by the light extinction at 532 nm. The extraction efficiency of the USN showed a broad maximum of about 10% in the diameter range 200–500 nm and decreased substantially at larger sizes. The accuracy and reproducibility of the measured mass concentration of BC in sample water after long-term storage were about ±25% and ±35%, respectively. We tested the method by analyzing rainwater and surface snow samples collected in Okinawa and Sapporo, respectively. The measured number size distributions of BC in these samples showed negligible contributions of BC particles larger than 300 nm to the total number of BC particles. A dominant fraction of BC mass in these samples was observed in the diameter range 100–500 nm.

Copyright 2013 American Association for Aerosol Research  相似文献   
108.
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110.
The Single Particle Soot Photometer (SP2) is an instrument for quantifying the refractory black carbon (rBC) mass of individual aerosol particles. It heats the particle’s rBC component to vaporization and quantifies the resulting visible thermal radiation to infer rBC mass. For purely technical reasons, SP2s are unable to quantify rBC mass beyond an easily adjustable limit due to eventual saturation of the electronics that record the visible light signals. Here, we evaluate an extrapolation algorithm to estimate rBC masses exceeding this upper limit in an SP2. The algorithm is based on identifying the crossing points of linear fits to unsaturated data, and using the duration of the saturated data to constrain potential errors. We find that extrapolation performance is quite insensitive to instrument parameters including laser intensity, rate of data acquisition, and particle speed through the laser. However, this approach increases uncertainty on the detection limit of the instrument, and is hence only useful in unknown aerosols for very limited extrapolation to approximately a factor of 1.5 increase in the upper mass range, corresponding to a 15% increase in the upper diameter limit. This increased range small enough that early identification of meaningful saturation during measurement campaigns remains the only tenable approach to robustly characterizing rBC mass size distributions and, in some cases, rBC mass concentrations.  相似文献   
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