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51.
LaF3 superfine powder was synthesized from La(CH3COO)3 and NH4 F by microwave heating method,using ethanol or pure water as dispersants respectively. The results of XRD and SEM indicate that the superfine powder has high purity, regular particle shape and narrow distribution of granularity. The granularity of the best sample is in the range of 100 -200 nm. The influence of different dispersants on the crystal degree and microstructure was discussed. After the superfine powder was formed into a slice at pressure of 25 - 60 MPa, its electrochemical impedance spectroscopy was tested by electrochemical impedance spectroscopy (EIS) measurement. The result shows that the grain refining of LaF3 powder increases its ionic conductivity. Compared with traditional preparation methods of LaF3 powder, the advantages of microwave heating method were summarized. 相似文献
52.
碳钢与不锈钢在腐蚀浆料中冲刷腐蚀交互作用的定量研究 总被引:1,自引:1,他引:1
用失重法和电化学法系统地研究了碳钢与不锈钢在腐蚀浆料中冲刷与腐蚀的交互作用及其电化学行为。试验表明:①冲刷腐蚀和动态纯腐蚀极化曲线与静态纯腐蚀极化曲线截然不同,两者的腐蚀机理存在本质的差异;②T8钢以腐蚀失重为主,18—8不锈钢以冲刷失重为主,两者的冲刷腐蚀交互作用失重率占其总失重率的60%以上,表明耐蚀不耐磨的18—8不锈钢和耐磨不耐蚀的T8钢在冲刷腐蚀工况中均难以胜任;③T8钢的冲刷腐蚀失重率和交互作用失重平均是18—8不锈钢的6倍以上,表明在液固两相流冲刷腐蚀工况中,材料必须首先具有一定的耐蚀性,然后再考虑提高材料的硬度和耐磨性,这样才能有效地提高材料的耐冲刷腐蚀性能。 相似文献
53.
To improve the cycle performance of eco-friendly and cost-effective spinel LiMN2O4 as the Li secondary batteries, the Th-doped LiThxMn1-xO4 spinel powers were synthesized by solid-state method. The starting materials, Li2CO3,MnO2 and Th(NO3)4·4H2O, were mixed uniformly using a traditional ball milling, which resulted in a uniform particle size distribution in the mixed powers. Tests of X-ray diffraction, SEM, impedance spectra and charge-discharge were carried out for LiThxMn1-xO4 cathode materials. Results show that the synthesized LiTh0.01Mn1.99O4 material exhibits standard spinel structure, regular particle morphology and excellent property of charge-discharge for big current. The capacity retention of the material modified by doping Th is more than 85.1% of the first discharge specific capacity of 111.5 mAh·g -1 after 20 cycles at the current rate 1C, while the pristine LiMN2O4 is only 57% of the first discharge specific capacity of 110.2 mAh·g-1 after the same cycles at the same current rate. 相似文献
54.
G. X. Zhao M. Zheng X. H. Lv X. H. Dong H. L. Li 《Metals and Materials International》2005,11(2):135-140
The corrosion behavior of 13Cr martensitic stainless steel in a CO2 environment in a stimulated oilfield was studied with potentiodynamic polarization and the impedance spectra technique. The
results showed that the microstructure of the surface scale clearly changed with temperature. This decreased the sensitivity
of pitting corrosion and increased the tendency toward general (or uniform) corrosion. The capacitance, the charge transfer
resistance, and the polarization resistance of the corrosion product scale decrease with increasing temperature from 90 to
120 °C, and thus the corrosion is a thermal activation controlled process. Charge transfer through the scale is difficult
and the corrosion is controlled by a diffusion process at a temperature of 150 °C. Resistance charge transfer through the
corrosion product layer is higher than that in the passive film. 相似文献
55.
56.
The concept of non-faradaic electrochemical modification of catalytic activity (NEMCA) has been applied for the in situ control of catalytic activity of a rhodium film deposited on YSZ (yttria stabilized zirconia) solid electrolyte towards reduction of 1000 ppm NO by 1000 ppm C3H6 in presence of excess (5000 ppm) O2 at 300 °C. A temporary heating at this feed composition results in a long-lasting deactivation of the catalyst under open circuit conditions due to partial oxidation of the rhodium surface. Positive current application (5 A) over both the active and the deactivated catalysts gives rise to an enhancement of N2 and CO2 production, the latter exceeding several hundred times the faradaic rate. While active rhodium exhibits a reversible behaviour, electrochemical promotion on the deactivated catalyst is composed of a reversible and an irreversible part. The reversible promotion results from the steady-state accumulation of current-generated active species at the gas exposed catalyst surface whereas the irreversible effect is due to the progressive reduction of the catalyst resulting in an increased recovery rate of lost catalytic activity. The results are encouraging with respect to application of rhodium for the catalytic removal of NO from auto-exhaust gases under lean-burn conditions. 相似文献
57.
垂直管内弹状气泡上升中壁面传递的实验研究 总被引:2,自引:0,他引:2
垂直管内弹状流壁面传递是诸多工业应用中需研究的重要问题之一。今用极限扩散电流技术,对弹状气泡上升时瞬时壁面剪应力和传质系数进行了测定,结果显示:当基于表观气速的Froude数FrG < 0.74时,壁面剪应力随弹状气泡和液塞的到来呈现方向相反的交替变化,壁面传质系数亦相应变化;而当FrG > 0.74时,剪应力方向一直向下,说明液膜向下流动,且弹状气泡和液塞的到来对壁面传质系数的影响很小。这说明下落液膜射流穿透了液塞段,控制了整个壁面传递过程。研究还对下落液膜区、尾迹区及液塞段的不同传递特征及机理进行了分析, 并结合气泡塔熔融结晶器中弹状气泡上升时的传热,对结晶操作条件的合理选择进行了讨论。 相似文献
58.
通过X射线衍射谱(XRD)、气态吸放氢行为(PCT曲线)、电化学充放电性能、电化学阻抗谱(EIS),考察了Ni添加对Ti_(0.47)V_(0.28)Mn_(0.15)Cr_(0.1)储氢合金的电化学性能的影响。结果表明:Ti_(0.47)V_(0.28)Mn_(0.15)Cr_(0.1)的电化学活性很差,在碱液中几乎不能放电,添加Ni之后得到了明显改善。随着Ni含量的增加,Ti_(0.47)V_(0.28)Mn_(0.15)Cr_(0.1)Ni_x(x=0~0.25)合金电极的放电容量先增大后减小,在x=0.15时达到最大值310mA·h·g~(-1)。 相似文献
59.
Poly(5‐bromoindole) (PBrI) films were synthesized electrochemically by direct oxidation of 5‐bromoindole in pure boron trifluoride diethyl etherate. The oxidation potential of 5‐bromoindole in this medium was measured to be only 0.97 V vs. saturated calomel electrode, which was lower than that determined in acetonitrile + 0.1 mol L?1 Bu4NBF4 (1.08 V). PBrI films obtained from this medium showed good electrochemical behavior and good thermal stability. Structural studies showed that the polymerization of 5‐bromoindole ring occurred at 2,3 position. As‐formed PBrI films were thoroughly soluble in strong polar solvent dimethylsulfoxide and partly soluble in tetrahydrofuran. Fluorescent spectral studies indicated that PBrI was a good blue‐light emitter. The excitation and emission spectra of PBrI showed a significant shift to longer wavelength compared with that of the monomer, consistent with the greater extent of electron delocalization. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 539–547, 2006 相似文献
60.