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61.
Impact of the Cd2+ treatment on the electrical properties of Cu2ZnSnSe4 and Cu(In,Ga)Se2 solar cells
Khaled Ben Messaoud Marie Buffire Guy Brammertz Hossam ElAnzeery Souhaib Oueslati Jonathan Hamon Bas J. Kniknie Marc Meuris Mosbah Amlouk Jef Poortmans 《Progress in Photovoltaics: Research and Applications》2015,23(11):1608-1620
The present contribution aims at determining the impact of modifying the properties of the absorber/buffer layer interface on the electrical performance of Cu2ZnSnSe4 (CZTSe) thin‐film solar cells, by using a Cd2+ partial electrolyte (Cd PE) treatment of the absorber before the buffer layer deposition. In this work, CZTSe/CdS solar cells with and without Cd PE treatment were compared with their respective Cu(In,Ga)Se2 (CIGSe)/CdS references. The Cd PE treatment was performed in a chemical bath for 7 min at 70 °C using a basic solution of cadmium acetate. X‐ray photoemission spectroscopy measurements have revealed the presence of Cd at the absorber surface after the treatment. The solar cells were characterized using current density–voltage (J–V), external quantum efficiency, and drive‐level capacitance profiling measurements. For the CZTSe‐based devices, the fill factor increased from 57.7% to 64.0% when using the Cd PE treatment, leading to the improvement of the efficiency (η) from 8.3% to 9.0% for the best solar cells. Similar observations were made on the CIGSe solar cell reference. This effect comes from a considerable reduction of the series resistance (RS) of the dark and light J–V, as determined using the one‐diode model. The crossover effect between dark and light J–V curves is also significantly reduced by Cd PE treatment. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
62.
Khaled Benelhadj-Said 《中国油气》2021,(1):53-57
正From March 1 to 5, the 2021 "Cambridge Energy Week"(CERAWEEK) meeting was held online.With the theme of "The New Map: Energy, Climate and Charting the Future", this "Cambridge Energy Week"discusses energy transformation, geopolitics,economy and market, investment and fnancing, innovation and technology, and talents needed in the future. 相似文献
63.
Anjela Manandhar Mona H. Haron Samir A. Ross Michael L. Klein Khaled M. Elokely 《International journal of molecular sciences》2022,23(8)
Vitamin E acetate, which is used as a diluent of tetrahydrocannabinol (THC), has been reported as the primary causative agent of e-cigarette, or vaping, product use-associated lung injury (EVALI). Here, we employ in vitro assays, docking, and molecular dynamics (MD) computer simulations to investigate the interaction of vitamin E with the membrane-bound cannabinoid 2 receptor (CB2R), and its role in modulating the binding affinity of THC to CB2R. From the MD simulations, we determined that vitamin E interacts with both CB2R and membrane phospholipids. Notably, the synchronized effect of these interactions likely facilitates vitamin E acting as a lipid modulator for the cannabinoid system. Furthermore, MD simulation and trajectory analysis show that when THC binds to CB2R in the presence of vitamin E, the binding cavity widens, facilitating the entry of water molecules into it, leading to a reduced interaction of THC with CB2R. Additionally, the interaction between THC and vitamin E in solution is stabilized by several H bonds, which can directly limit the interaction of free THCs with CB2R. Overall, both the MD simulations and the in vitro dissociation assay results indicate that THC binding to CB2R is reduced in the presence of vitamin E. Our study discusses the role of vitamin E in limiting the effect of THCs and its implications on the reported pathology of EVALI. 相似文献
64.
K. F. Khaled 《Journal of Applied Electrochemistry》2009,39(3):429-438
Electrochemical frequency modulation, EFM is a new technique for corrosion rate measurements. With the EFM technique, the
corrosion rate and corrosion kinetic parameters can be obtained instantaneously without prior knowledge of Tafel slopes, which
makes this method an ideal technique for application as a corrosion monitoring tool. Results obtained with the EFM technique
were shown to be in agreement with chemical (weight loss) and electrochemical methods (Tafel extrapolation and electrochemical
impedance spectroscopy, EIS) for corrosion rate measurements. New synthesized hydrazine carbodithioic acid derivatives namely,
N′-furan-2-yl-methylene-hydrazine carbodithioic acid (A), N′-(4-dimethylamino-benzylidene)-hydrazine carbodithioic acid (B) and N′-(3-nitro-benzylidene)-hydrazine carbodithioic acid (C) were examined as corrosion inhibitors for carbon steel in 1 M perchloric
acid solution. The results obtained from both chemical and electrochemical measurements show that these compounds suppressed
both anodic and cathodic processes of carbon steel corrosion in 1 M HClO4 by adsorption on the electrode surface. The adsorption mode follows the Langmuir adsorption isotherm. The efficiency of the
inhibitors increases in the order C > B > A. 相似文献
65.
Liquid‐phase axial dispersion of turbulent gas–liquid co‐current flow through screen‐type static mixers 下载免费PDF全文
This article discusses the characteristics of turbulent gas–liquid flow through tubular reactors/contactors equipped with screen‐type static mixers from a macromixing perspective. The effect of changing the reactor configuration, and the operating conditions, were investigated by using four different screen geometries of varying mesh numbers. Residence time distribution experiments were conducted in the turbulent regime (4500 < Re < 29,000). Using a deconvolution technique, the RTD function was extracted to quantify the axial/longitudinal liquid‐phase dispersion coefficient. The findings highlight that axial dispersion increases with an increasing flow rate and/or gas‐phase volume fraction. However, regardless of the number and geometry of the mixing elements, reactor configuration, and/or operating conditions, the recorded liquid‐phase axial dispersion coefficients in the presence of screens was lower than that for an empty pipe. Furthermore, the geometry of the screen was found to directly affect the axial dispersion coefficient in the reactor. © 2016 American Institute of Chemical Engineers AIChE J, 63: 1390–1403, 2017 相似文献
66.
67.
The corrosion inhibition of Cu-Ni alloys was investigated in aqueous chloride solutions using amino acids as environmentally safe materials. The corrosion rate was calculated in absence and presence of the corrosion inhibitor using polarization and impedance techniques. The inhibition efficiency of the different amino acids was also calculated.The experimental results have shown that a simple amino acid like glycine can be used as efficient corrosion inhibitor for the Cu-Ni alloys in neutral chloride solutions. An inhibition efficiency of about 85% could be achieved at very low concentrations of the amino acid (0.1 mM). For low Ni content alloy (Cu-5Ni), 2.0 mM cysteine shows a remarkable high (∼96%) corrosion inhibition efficiency. The experimental impedance data were fitted to theoretical data according to a proposed equivalent circuit model for the electrode/electrolyte interface, and the mechanism of the corrosion inhibition process was suggested. Different adsorption isotherms were tested and the corrosion inhibition process was found to depend on the adsorption of the amino acid molecules and/or the deposition of corrosion products on the alloy surface. The adsorption free energy of cysteine on Cu-5Ni (−37.81 kJ mol−1) reveals a strong physical adsorption of the inhibitor on the alloy surface. 相似文献
68.
The present numerical study concentrates on the effects of moderate and high Reynolds numbers on the laminar flow of a non-Newtonian rigid viscoplastic (Bingham) fluid through a sudden contraction in a pipe. The flow is assumed to be steady, incompressible, and isothermal. Results are presented for a wide range of the governing Reynolds and yield numbers and the significant effects of these two parameters both on the integral and local kinematic properties of the flow field are established. Low yield numbers result in the disappearance of the recirculating flow region at the corner replacing it with a region of very low rates of deformation. The evolution of the centerline velocity in the vicinity of the contraction plane is shown to be independent of the yield number and dependent on the Reynolds number, while the concavities in the streamwise velocity profiles appearing at high Reynolds numbers are independent of the yield number. The pressure losses through the contraction increase with yield number with the effect being more pronounced at lower Reynolds numbers. 相似文献
69.
Adsorption of nitrate and monovalent phosphate anions from aqueous solutions on mono, di‐ and tri‐ammonium‐functionalised mesoporous SBA‐15 silica was investigated. The adsorbents were prepared via a post‐synthesis grafting method, using either 3‐aminopropyltrimethoxysilane (N‐silane) or [1‐(2‐aminoethyl)‐3‐aminopropyl]trimethoxysilane (NN‐silane) or 1‐[3‐(trimethoxysilyl)‐propyl]‐diethylenetriamine (NNN‐silane), followed by acidification in HCl solution to convert the attached surface amino groups to positively charged ammonium moieties. The nominal loading of amino moieties on the SBA‐15 surface was varied from 5% to 20% as organoalkoxysilane/silica molar ratio. The adsorption experiments were conducted batchwise at room temperature. Results showed that adsorption capacity increased with increasing the concentration of monoammonium groups on the SBA‐15 adsorbent. Nitrate adsorption capacity increased from 0.34 to 0.66 mmol ${\rm NO}_{3}^{{-} } /{\rm g}$ adsorbent while phosphate adsorption capacity increased from 0.34 to 0.63 mmol ${\rm H}_{2} {\rm PO}_{4}^{{-} } /{\rm g}$ adsorbent when the molar ratio organoalkoxysilane/silica was varied from 5% to 20%, respectively. Also, for the same organoalkoxysilane/silica molar ratio of 10%, the adsorption capacity increased with the increase of the number of protonated amines in the functional groups. Therefore, maximum adsorption capacities of 0.80, 1.16 and 1.38 mmol ${\rm NO}_{3}^{{-} } /{\rm g}$ adsorbent and 0.72, 0.82 and 1.17 mmol ${\rm H}_{2} {\rm PO}_{4}^{{-} } /{\rm g}$ adsorbent were obtained using mono‐, di‐ and triammonium functionalised SBA‐15 adsorbents, respectively. © 2011 Canadian Society for Chemical Engineering 相似文献
70.
Khaled B Zitoun 《Chemical engineering science》2004,59(13):2767-2775
During continuous flow of solid-liquid mixtures, the solids may be oriented in a variety of directions relative to the flow axis. The character of the distribution takes on particular importance when materials are processed using electric fields. In this study, solids orientation distributions in continuous, vertical upflow was investigated experimentally combining particle tracking velocimetry. Cylindrical solids showed a more pronounced tendency than cubes to align along the flow direction; this tendency was even greater for elongated cylindrical objects. Solids orientation is influenced by the principal orienting factor (shear flow) and the randomizing factor (orientations of other solids in the mixture). Increasing flow rate tends to drag objects towards their equilibrium (aligned orientation) until they are restricted from further rotation by the presence of other solids. Orientations of cubes were more widely distributed than cylinders, without sharp peaks. The orienting effects of flow rate were also observed for cubes. High solids concentration and larger solids tend to restrict rotation, thus the initial distribution may be maintained through the flow length. 相似文献