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281.
282.
It has recently been reported that by using a spectral-tuning algorithm, the photocurrents of multiple detectors with spectrally overlapping responsivities can be optimally combined to synthesize, within certain limits, the response of a detector with an arbitrary responsivity. However, it is known that the presence of noise in the photocurrent can degrade the performance of this algorithm significantly, depending on the choice of the responsivity spectrum to be synthesized. We generalize this algorithm to accommodate noise. The results are applied to quantum-dot mid-infrared detectors with bias-dependent spectral responses. Simulation and experiment are used to show the ability of the algorithm to reduce the adverse effect of noise on its spectral-tuning capability.  相似文献   
283.
In this study, polyindole (PIN) and polyindole/polyethylene (PIN/PE) conducting composites, having various amounts of PIN, were synthesized by chemical polymerization using FeCl3 as an oxidizing agent and taking the ratio of salt:monomer as 3:1. The samples of PIN and PIN/PE composites were characterized by FTIR, UV–vis, TGA, SEM, Gouy scale magnetic susceptibility, conductivity (1.2 × 10−3 S cm−1 > σ > 1.96 × 10−6 S cm−1, at T = 25 °C) and density measurements. FTIR analysis suggested a 2,3-propagation mechanism for PIN formation. The ground milled samples were subjected to particle size analysis by dynamic light scattering (DLS) and a micron-sized particle distribution was obtained. A series of volume fractions ( = 10–25%) were prepared from the materials in silicone oil (SO) and their sedimentation stabilities determined. The most stable composite [PIN(89%)/PE(11%)] against gravitational sedimentation was subjected to flow-rate measurements under externally applied electric field strength (E) and an electrorheological (ER) activity was observed; threshold energies (Et) were calculated. The effects of volume fraction, shear rate, external E, frequency and temperature onto ER activities of the suspensions were investigated. Enhancement in the electric field viscosities and shear thinning viscoelastic behaviors were observed for all the samples studied. Recoverable viscoelastic deformations were determined from the creep tests under external E.  相似文献   
284.
Nanocomposite solid polymer films based on the poly(exo‐N‐phenyl‐7‐oxanorbornene‐5,6‐dicarboximide) (PPhONDI)/LiClO4/NiO system have been designed, and the effect of inorganic NiO nanofiller in different amounts on the film properties has been examined. The exo‐PPhONDI/LiClO4/NiO polymer system is the first solid nanocomposite polymer electrolyte film example based on a ring‐opening metathesis polymerization (ROMP) host polymer. The NiO nanoparticles were prepared by two‐step chemical syntheses, and the thermoplastic host polymer, exo‐PPhONDI, was synthesized via ROMP. Composite polymer films were prepared by the solution‐casting method. The amount of nanoparticles was varied from 1 to 15 wt % of NiO. The conductivity of the nanocomposite solid polymer systems was influenced by the NiO nanofiller concentration. The composite films based on exo‐PPhONDI ROMP polymer with the highest conductivity were achieved for the composition with 8 wt % of NiO nanofiller and 10 wt % of LiClO4 dopant. The prepared films were characterized using X‐ray diffraction, Fourier transform infrared spectroscopy, differential scanning calorimetry, and scanning electron microscopy (SEM). The SEM results showed that the filler was well distributed in the polymer matrix. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45938.  相似文献   
285.
Radical-initiated copolymerization of N-isopropyl acrylamide (NIPA) with maleic anhydride (MA) and macromolecular reactions of synthesized poly(NIPA-co-MA) with polyethyleneglycol (PEG with a methoxy chain end and molecular weight of 2000 g mol−1) and polyethyleneimine (PEI with molecular weight of 2000 g mol−1) have been studied as a way to obtain new reactive amphiphilic water-soluble polymers potentially useful as carriers for gene delivery. Structure, composition and thermal behaviour of synthesized copolymers and their macrobranched architectures are determined by FTIR, 1H and 13C NMR spectroscopy, elemental (N content) and chemical (acid number) analysis and differential scanning calorimetry, differential thermal and thermal gravimetric methods. It is shown that synthesized copolymers with given composition have low critical solution temperature (LCST) in the range of 30.2-46.4 °C at pH values of 4.0-7.4, which suggest the possibility of their biomedical applications.  相似文献   
286.
In this study, polyindene (PIn) and three PIn/organo‐montmorillonite (O‐MMT) nanocomposites namely K1: [PIn(94.5%)/O‐MMT(5.5%)], K2: [PIn(92.8%)/O‐MMT(7.2%)], and K3: [PIn(87.9%)/O‐MMT(12.1%)] were used to investigate the electrorheological (ER), creep‐recovery, and vibration damping characteristics. A volume fraction series (φ = 5–25%) of suspensions were prepared from the samples in silicone oil (SO). First, zeta (ζ)‐potentials and antisedimentation stabilities; second, ER properties of these nanocomposite/SO suspension systems were determined under externally applied electric field strengths. Besides, the effects of dispersed phase volume fraction, shear rate, electric field strength, and temperature onto ER performance of these suspensions were investigated and non‐Newtonian rheological behaviors were observed. The vibration damping capabilities of the suspensions were investigated using various rheological parameters on the electrorheometer and on an automobile shock absorber and a 66% vibration damping capacity were determined under an applied electric field strength, which is an important property from industrial point of view. Furthermore, the materials were subjected to creep and creep‐recovery tests and reversible viscoelastic deformations were determined. From the experiments carried out, the nanocomposites were classified as smart materials. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   
287.
Erroneous information from sensors affect process monitoring and control. An algorithm with multiple model identification methods will improve the sensitivity and accuracy of sensor fault detection and data reconciliation (SFD&DR). A novel SFD&DR algorithm with four types of models including outlier robust Kalman filter, locally weighted partial least squares, predictor-based subspace identification, and approximate linear dependency-based kernel recursive least squares is proposed. The residuals are further analyzed by artificial neural networks and a voting algorithm. The performance of the SFD&DR algorithm is illustrated by clinical data from artificial pancreas experiments with people with diabetes. The glucose-insulin metabolism has time-varying parameters and nonlinearities, providing a challenging system for fault detection and data reconciliation. Data from 17 clinical experiments collected over 896 h were analyzed; the results indicate that the proposed SFD&DR algorithm is capable of detecting and diagnosing sensor faults and reconciling the erroneous sensor signals with better model-estimated values. © 2018 American Institute of Chemical Engineers AIChE J, 65: 629–639, 2019  相似文献   
288.
Within the envelope function approach and the effective-mass approximation, we have investigated theoretically the effect of an intense, high-frequency laser field on the bound states in a GaxIn1 − xNyAs1 − y/GaAs double quantum well for different nitrogen and indium mole concentrations. The laser-dressed potential, bound states, and squared wave functions related to these bound states in Ga1 − xInxNyAs1 − y/GaAs double quantum well are investigated as a function of the position and laser-dressing parameter. Our numerical results show that both intense laser field and nitrogen (indium) incorporation into the GaInNAs have strong influences on carrier localization.  相似文献   
289.
The solid-state structure-property behavior of highly branched segmented poly(urethane urea) (PUU) copolymers and their linear analog was investigated. A limited study of their solution rheological behavior was also undertaken. The linear PUUs were synthesized by the two-step prepolymer method, whereas the oligomeric A2+B3 methodology was utilized to synthesize the highly branched materials. The soft segments (SS) were either poly(tetramethylene oxide) (PTMO) or poly(propylene oxide) (PPO). All copolymers utilized in this study, with one exception, contained 28 wt% hard segment (HS) content. DMA, SAXS, and AFM studies indicated that the linear as well as the highly branched PUUs were microphase separated. The SS Tg of the highly branched PUUs was nearly identical to that of their respective linear analogs. However, the linear copolymers exhibited broader and less temperature sensitive rubbery plateaus, both attributed to one or both of two reasons. The first is better hydrogen bonding organization of the HS phase as well as greater HS lengths than in the highly branched analogs. The second parameter is that of a potentially higher chain entanglement for the linear systems relative to the branched analogs. Tapping-mode AFM phase images confirmed the microphase morphology indicated by SAXS and DMA. Ambient temperature strain-induced crystallization was observed in the PUU based on PTMO 2040 g/mol at a uniaxial strain of ca. 400%, irrespective of the chain architecture. Stress-strain, stress relaxation, and mechanical hysteresis of the highly branched copolymers were in general slightly poorer than that of their linear analogs. Ambient temperature solution viscosity of the highly branched materials in dimethyl formamide was substantially lower that that of the linear samples of nearly equal molecular weight.  相似文献   
290.
S. Unal  E. Yilgor  T.E. Long 《Polymer》2005,46(13):4533-4543
Structure development in highly branched segmented polyurethaneureas based on oligomeric A2+B3 approach was investigated by experimental studies and kinetic Monte-Carlo simulations. In both simulations and experiments, hyperbranched polymers were produced by the slow addition of A2 onto B3. Experimental studies showed strong influence of solution concentration on the gel point and the extent of cyclization in the polymers formed. In polymerizations conducted at a solution concentration of 25% by weight gelation took place at the stoichiometric ratio [A2]/[B3]=0.886. This is somewhat higher than the theoretical ratio of 0.75. In very dilute solutions, such as 5% solids by weight, no gelation was observed although the stoichiometric amount of A2 added well exceeded the theoretical amount for gelation. Both experimental studies by size exclusion chromatography (SEC) and kinetic Monte-Carlo simulations demonstrated a gradual increase in polymer molecular weights as more A2 is added onto B3. This was followed by a sharp increase in the polymer molecular weight as the gel point is approached. A very similar behavior was observed for the polydispersity values of the polymers formed. Kinetic Monte-Carlo simulations performed at different cyclization ratios showed very good agreement with experimental results.  相似文献   
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