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61.
The antioxidant, phenol, ascorbic acid, electrode corrosion and engineering factors of concentration process of kiwifruit juice by ohmic heating-vacuum conditions (OHVC) were evaluated and compared with ohmic heating under atmospheric conditions (OHAC). Results showed that the total phenol content was decreased with an increasing voltage gradient for both heating modes. The OHVC can better save the antioxidant capacity and ascorbic acid of concentrated samples than the OHAC. The processing time of OHVC was significantly higher than the OHAC at the same voltage gradient (P < 0.05). The electrode corrosion rate at the vacuum mode was 7- to 40-fold higher than the atmospheric mode. The energy efficiency at OHAC was lower than the OHVC. The energy consumption was found in the range of 3.37 to 3.75 MJ kg−1 water for OHAC and 4.08 to 11.09 MJ kg−1 water for OHVC. The electrical conductivity under the vacuum mode was lower than the atmospheric mode.  相似文献   
62.
A proton exchange membrane was synthesized consuming a sodium alginate biopolymer as the matrix and titanium oxide as the nanofiller. The titanium oxide content varied from 5 to 25 wt%. The biomembrane nanocomposite performs better than the pristine sodium alginate membrane based on liquid uptake, methanol permeability, proton conductivity, ion exchange capacity, and oxidative stability outcomes. The unique properties of sodium alginate and titanium oxide lead to outstanding interconnections, thus producing new materials with great characteristics and enhanced performance. The highest proton conductivity achieved in this study is 17.3 × 10‐3 S cm‐1, which performed by SAT5 (25 wt%) membranes at 70°C. An optimal content of titanium oxide enhances the conductivity and methanol permeability of the membrane. Additionally, the hydrophilicity of pure sodium alginate is greatly reduced and achieves a good liquid uptake capacity and swelling ratio. The characteristics of the SA/TiO2 biomembrane nanocomposite were determined with field emission scanning electron microscope, Fourier transform infrared, X‐ray diffraction, thermal gravimetric analysis/differential scanning calorimetry, and mechanical strength analysis.  相似文献   
63.
In this work, we have synthesized a series of quaternary ammonium from amino alcohols and n-bromoalkanes. The compounds are referred to as CnEtOH, CnPrOH, and CniPrOH (where n = 12 and 14 carbons, EtOH = ethanol, PrOH = propanol, iPrOH = iso-propanol). Their structures were checked using the usual spectroscopic methods [1H, 13C nuclear magnetic resonance (NMR) and infrared (IR)]. Their physicochemical properties in aqueous solution were studied using conductivity, surface tension, and ultra violet (UV)–visible absorption spectroscopy measurements. This study was conducted to show the effect of the linear hydrophobic chain and the location of the OH polar group with respect to the N+ quaternary ammonium on the physicochemical properties of the surfactants. The comparison between the physicochemical properties of the surfactants studied shows a distinct effect of the position of the OH group on the critical micelle concentration (CMC), the ionization degree (α), the area occupied at the interface (Amin), the free energy of adsorption (), and the free energy of micellization (). The intermolecular interaction between the synthetic surfactants and the methyl orange (OM) dye is related to the degree of hydration of the micelle, proven by the hypsochromic displacement of OM wavelength (λmax) and ionization (α) of the micelles. The CMC, the degree of ionization, and the degree of hydration of the micelle follow the same trend.  相似文献   
64.
Graphene oxide (GO) nanosheets are introduced to a Quaternized polyvinyl alcohol (QPVA) polymer matrix to obtain an anion exchange membranes (AEMs) for application of fuel cells. QPVA/GO nanocomposite membranes provide desirable properties such as low fuel uptake and permeability, excellent ionic conductivity, and cell performance, all of which are favorable for AEMs based on our previous works. Passive direct methanol fuel cells (DMFCs) are recognized as suitable technologies for use in portable devices. Nevertheless, the commercialization of DMFCs remains restricted due to a number of issues related to the conventional membrane; one of these issues is high fuel crossover problems due to high fuel uptake and permeability of Nafion membrane. This study aimed to expand the potential applications of QPVA/GO nanocomposite membranes in air-breathing passive DMFCs. The ionic conductivity, methanol uptakes (MUs), and permeabilities of self-synthesis QPVA/GO nanocomposites are examined to evaluate the ability to operate in methanol atmosphere. At 30°C, the ionic conductivity of the membranes reached 1.74 × 10−2 S cm−1. The MUs and permeabilities were as low as 35% and 7.6 × 10−7 cm2 s−1, respectively. The performance of air-breathing passive DMFCs bearing QPVA/GO nanocomposite membrane is much higher compared to conventional membranes. The maximum power density of air-breathing passive DMFCs was achieved 27.2 mW cm−2 under the optimum condition of 2 M methanol + 4 M KOH at 70°C. Single-cells could be sustained for 1000 hours. This article is the first to optimize and highlight the performance air-breathing passive DMFCs by using a QPVA-based membrane.  相似文献   
65.
66.
Extensive cracking of the type known as stack cracking was demonstrated in a cathodically charged X65 microalloyed pipeline steel containing a weldment. It is shown that the formation and propagation of rolling-plane cracks, which constitute the primary stages of the stack cracking, is due to local concentration of hydrogen gas pressure and a lowering of the cohesive strength of a number of interfaces by hydrogen. The characteristic S-shape of individual cracks which occurred during the linking up of cracks was attributed to stress interactions at crack tips and cleavage cracking normal to the rolling plane. An explanation of hydrogen embrittlement fracture is given in terms of electronic state modifications of the steel, including charge polarization.  相似文献   
67.
In this study, the physicomechanical properties and morphology evolution of irradiated (styrene butadiene rubber)/(devulcanized waste rubber)/(organically modified montmorillonite) nanocomposites were realized. The improvement in the physicomechanical properties provides a possible mechanism on how organically modified montmorillonite influences the general properties of irradiated nanocomposites. X‐ray diffraction data illustrated that there is an increase in the basal spacing of sodium montmorillonite clay due to modification and/or polymer intercalation. The results of mechanical properties showed that the as‐prepared nanocomposites have superior irradiation‐resistant properties to the (styrene butadiene rubber)/(devulcanized waste rubber) blend. J. VINYL ADDIT. TECHNOL., 24:50–57, 2018. © 2015 Society of Plastics Engineers  相似文献   
68.
Masking schemes based on tables recomputation are classical countermeasures against high-order side-channel attacks. Still, they are known to be attackable at order d in the case the masking involves d shares. In this work, we mathematically show that an attack of order strictly greater than d can be more successful than an attack at order d. To do so, we leverage the idea presented by Tunstall, Whitnall and Oswald at FSE 2013: We exhibit attacks which exploit the multiple leakages linked to one mask during the recomputation of tables. Specifically, regarding first-order table recomputation, improved by a shuffled execution, we show that there is a window of opportunity, in terms of noise variance, where a novel highly multivariate third-order attack is more efficient than a classical bivariate second-order attack. Moreover, we show on the example of the high-order secure table computation presented by Coron at EUROCRYPT 2014 that the window of opportunity enlarges linearly with the security order d. These results extend that of the CHES ’15 eponymous paper. Here, we also investigate the case of degree one leakage models and formally show that the Hamming weight model is the less favorable to the attacker. Eventually, we validate our attack on a real ATMEL smartcard.  相似文献   
69.
Based on theoretical calculations on solute exchange capacities of various peritoneal tissues, the liver has been predicted to account for up to 43% of the permeability-surface area product (PS) of the entire peritoneal "membrane" for a small solute (sucrose) during peritoneal dialysis (PD). In these calculations, the abdominal wall and the diaphragm were found to contribute only approximately 10 to 15% of the total PS. However, evisceration has in previous studies been shown to affect the PS characteristics during PD only marginally (10 to 30%). In such evisceration experiments the liver was usually not removed, and therefore it has been suggested that an intact liver might have significantly contributed to the solute exchange under these premises. We assessed the peritoneal PS of 51Cr-EDTA (constantly infused intravenously) and the plasma-to-peritoneal clearance (ClB-->P) of 125I-human serum albumin (RISA) (given as an i.v. bolus) in Wistar rats during acute PD. In one group of rats the liver surface was sealed off using Histoacrylate glue (N = 6) and in another group a 90% hepatectomy was performed, the remaining portion of the liver, usually the right lower lobe, being sealed off by glue (N = 6). A third group was sham operated to serve as control (N = 12). The PS for 51Cr-EDTA was 0.32 +/- 0.03(+/- SE) ml. min-1 (N = 12) during control, 0.32 +/- 0.04 ml.min-1 after "sealing" of the liver surface (N = 6, P > 0.1) and 0.40 +/- 0.03 after hepatectomy (N = 6, P > 0.1), that is, remained unchanged after experimental intervention. The CIB-->P of RISA during control was 5.88 +/- 1.0 microliter.min-1 (N = 10), and was not altered after hepatectomy, 6.17 +/- 0.48 microliters.min-1 (N = 5, P > 0.1), but slightly increased after liver surface sealing (9.69 +/- 1.09 microliters.min-1, N = 5, P < 0.05). In conclusion, the present experiments indicate that the liver does not play an essential role in the overall solute exchange between the plasma and the peritoneal cavity (PC) during PD.  相似文献   
70.
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