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11.
Factors which might affect the absorption of vitamin K of dietary origin were investigated using everted small bowel sacs. Increasing the bile salt concentration to 20 mM or the addition of long chain fatty acids, monoolein, or lecithin all resulted in significant (P less than 0-05) decrease in the absorption rate of the vitamin. The addition of 2-5 mM short and medium chain fatty acids did not change the absorption rate of vitamin K-1 (P greater than 0-05). The absorption rate of vitamin K-1 appears to be modified by the presence of compounds in the incubation medium which either alter the partition of the vitamin between the micelle and the cell membrane or which change the permeation characteristics of the compound through the unstirred water layer or modify the physical characteristics of the cell membrane itself. It is possible that some of the above factors modify the absorption of lipid soluble compounds in general.  相似文献   
12.
The comparison of resistive switching (RS) storage in the same device architecture is explored for atomic layer deposition (ALD) Al2O3, HfO2 and HfAlOx‐based resistive random access memory (ReRAM) devices. Among them, the deeper high‐ and low‐ resistance states, more uniform VSETVRES, persistent ROFF/RON (>102) ratio and endurance up to 105 cycles during both DC and AC measurements were observed for HfAlOx‐based device. This improved behavior is attributed to the intermixing of amorphous Al2O3/HfO2 oxide layers to form amorphous thermally stable HfAlOx thin films by consecutive‐cycled ALD. In addition, the higher oxygen content at Ti/HfAlOx thin films interface was found within the energy dispersive spectroscopy analysis (EDS). We believe this higher oxygen content at the interface could lead to its sufficient storage and supply, leading to the stable filament reduction‐oxidation operation. Further given insight to the RS mechanism, SET/RESET power necessities and scavenging effect shed a light to the enhancement of HfAlOx‐based ReRAM device as well.  相似文献   
13.
The orientation of the noncrystalline (amorphous) phase in poly(ethylene terephthalate) fibers is analyzed by separating the amorphous scattering in the wide-angle x-ray diffraction patterns into isotropic and anisotropic components. Two parameters are used to characterize the amorphous orientation—the fraction of the anisotropic component and its degree of orientation. The x-ray amorphous orientation parameters are compared with the sonic modulus and the birefringence values. Our results illustrate that the intrinsic birefringence of the amorphous phase is not “intrinsic” but depends on its density. The role of the oriented amorphous phase in determining the strength (tenacity) and the dimensional stability (shrinkage) of the fibers is discussed. We conclude that although amorphous orientation determines the shrinkage, other factors such as the connectivity between the amorphous phase and the crystalline regions play an important role in determining the tenacity of the fibers. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 64: 1363–1371, 1997  相似文献   
14.
The majority of approaches to activity recognition in sensor environments are either based on manually constructed rules for recognizing activities or lack the ability to incorporate complex temporal dependencies. Furthermore, in many cases, the rather unrealistic assumption is made that the subject carries out only one activity at a time. In this paper, we describe the use of Markov logic as a declarative framework for recognizing interleaved and concurrent activities incorporating both input from pervasive lightweight sensor technology and common-sense background knowledge. In particular, we assess its ability to learn statistical-temporal models from training data and to combine these models with background knowledge to improve the overall recognition accuracy. We also show the viability and the benefit of exploiting both qualitative and quantitative temporal relationships like the duration of the activities and their temporal order. To this end, we propose two Markov logic formulations for inferring the foreground activity as well as each activities’ start and end times. We evaluate the approach on an established dataset where it outperforms state-of-the-art algorithms for activity recognition.  相似文献   
15.
Transition metal dichalcogenides (TMDs) van der Waals (vdW) 1D heterostructures are recently synthesized from 2D nanosheets, which open up new opportunities for potential applications in electronic and optoelectronic devices. The most recent and promising strategies in regards to forming 1D TMDs nanotubes (NTs) or nanoscrolls (NSs) in this review article as well as their heterostructures that are produced from 2D TMDs are summarized. In order to improve the functionality of ultrathin 1D TMDs that are coaxially combined with boron nitride nanotubes and single-walled carbon nanotubes. 1D heterostructured devices perform better than 2D TMD nanosheets when the two devices are compared. The photovoltaic effect in WS2 or MoS2 NTs without a junction may exceed the Shockley–Queisser limit for the above-band-gap photovoltage generation. Photoelectrochemical hydrogen evolution is accelerated when monolayer WS2 or MoS2 NSs are incorporated into a heterojunction. In addition, the photovoltaic performance of the WSe2/MoS2 NSs junction is superior to that of the performance of MoS2 NSs. The summary of the current research about 1D TMDs can be used in a variety of ways, which assists in the development of new types of nanoscale optoelectronic devices. Finally, it also summarizes the current challenges and prospects.  相似文献   
16.
The transference and reactivity of proanthocyanidins is an important issue that affects the technological processing of some fruits, such as grapes and apples. These processes are affected by proanthocyanidins bound to cell wall polysaccharides, which are present in high concentrations during the processing of the fruits. Therefore, the effective extraction of proanthocyanidins from fruits to their juices or derived products will depend on the ability to manage these associations, and, in this respect, enzymes that degrade these polysaccharides could play an important role. The main objective of this work was to test the role of pure hydrolytic enzymes (polygalacturonase and cellulose) and a commercial enzyme containing these two activities on the extent of proanthocyanidin-cell wall interactions. The results showed that the modification promoted by enzymes reduced the amount of proanthocyanidins adsorbed to cell walls since they contributed to the degradation and release of the cell wall polysaccharides, which diffused into the model solution. Some of these released polysaccharides also presented some reactivity towards the proanthocyanidins present in a model solution.  相似文献   
17.
18.
The present study aimed to evaluate the effect of bioactive glass as well as the presence of Ciprofloxacin drug (%Cip) into bioactive glass–chitosan composite on the in vivo behavior of these scaffolds. These scaffolds were implanted in the femoral condyl of an ovariectomized rat. The serum and organs (liver and kidney) of the under investigated rats were analyzed. Also the physicochemical properties of the prepared implants were assessed using Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) before and after implantation (at different periods of implantation). Biochemical and histological analyses of the under investigated rats proved the biocompatibility of the prepared scaffolds. The hydroxyapatite like layer was significantly precipitated on the surface of BG–CH scaffold than BG–CH–20Cip. In this same period, FT-IR of BG–CH shows complete disappearance of Si–O–Si. Their characteristics bands were replaced by P–O group arisen form bone apatite bands. Physicochemical results show progressive degradation of BG–CH and BG–CH–20Cip that occurred at the same time as replacement of the implant by an apatite layer. However, the bioresorbability and bioactivity of BG–CH are faster than those of BG–CH–20Cip. Therefore, the incorporation of the Ciprofloxacin in the BG–CH induces a retarding effect on the formation of the hydroxyapatite, and consequently on the ossification, without any side effects on the liver–kidney.  相似文献   
19.
Cathode active materials with a composition of LiNi0.9Co0.1O2 were synthesized by a solid-state reaction method at 850 °C using Li2CO3, NiO or NiCO3, and CoCO3 or Co3O4, as the sources of Li, Ni, and Co, respectively. Electrochemical properties, structure, and microstructure of the synthesized LiNi0.9Co0.1O2 samples were analyzed. The curves of voltage vs. x in LixNi0.9Co0.1O2 for the first charge–discharge and the intercalated and deintercalated Li quantity Δx were studied. The destruction of unstable 3b sites and phase transitions were discussed from the first and second charge–discharge curves of voltage vs. x in LixNi0.9Co0.1O2. The LiNi0.9Co0.1O2 sample synthesized from Li2CO3, NiO, and Co3O4 had the largest first discharge capacity (151 mA h/g), with a discharge capacity deterioration rate of −0.8 mA h/g/cycle (that is, a discharge capacity increasing 0.8 mA h/g per cycle).  相似文献   
20.
BACKGROUND: This study concerns the assessment of laccase stability during textile industry effluent treatment by laccase in the presence of a mediator RESULTS: The effects of 1‐hydroxybenzotriazole (HBT) and textile wastewater on the stability of a crude laccase prepared from cultures of Trametes trogii during the process of textile industry effluent decolourization were determined. HBT was essential for decolourization of effluent by laccase. Decolourization efficiency decreased when effluent was repeatedly added to the reaction mixture, suggesting inhibition of laccase during the process. Stability of the laccase was not affected by different concentrations of effluent, but inactivation was proportional to HBT concentration. CONCLUSION: Experimental results showed that a redox mediator such as HBT was required for high decolourization rate of textile industry effluent; however free radicals generated from this compound inactivated the laccase used in the process. Copyright © 2009 Society of Chemical Industry  相似文献   
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