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31.
32.
高能球磨LaNi5-34%(质量分数)Mg的相组成与热稳定性能 总被引:1,自引:0,他引:1
采用X射线衍射仪(XRD)、扫描电子显微镜(SEM)、差热分析(DTA)等方法研究了高能球磨及热处理等对新型合金LaNi5-34%(质量分数)Mg的相组成、形貌及热稳定性能等的影响。结果表明:经100r/min球磨100h及190r/min球磨100h后,样品由La、Mg、Ni等非晶。微量的晶体Ni和MgNi2相组成,所得粉末的形状大多为规则的球形或近球形,其颗粒直径范围为0.05~33.0μm。球磨样品具有较好的室温活化特性,其最大电化学放电容量为460mAh/g。该样品经763K保温35d后,得到热稳定性较好的具有纳米尺度的MgNi2、Mg2Ni、Mg2NiLa三相组织,其平均晶粒直径为21.3nm。 相似文献
33.
甲烷制备高纯度氢气的实验研究 总被引:1,自引:0,他引:1
李传统 《南京师范大学学报》2004,4(4):28-31
对甲烷制备可供质子交换膜燃料电池(PEMFC)用的高纯度氢气进行了实验研究,得出了不同蒸汽/碳比值时甲烷的转化率、不同过量空气系数对制备气体成分的影响、不同压差时氢气在选择性膜中的渗透率以及不同系统压力对氢气反应焓的影响规律.研究结果表明,在蒸汽与甲烷中的碳比例一定时,蒸汽重整反应器内的反应速率和它出口处CO的浓度,随甲烷的流量的增加而提高.提高甲烷蒸汽重整系统的工作温度和压力,可以提高甲烷的转化率,在S/C比值不变的情况下,仅提高温度可提高甲烷的转化率约10%;而将工作压力由0.1MPa提高到0.6MPa,甲烷的转化率提高约21%.甲烷的理论转化率为84.6%,本文实验研究中的最大实际转化率为78.03%,实验研究系统的系统完善度为92.23%,说明该系统还有待完善之处,还可以进一步提高甲烷的转化率.增大PEMFC中选择性膜两侧的压差或提高氢气的纯度,均利于提高氢气混合物的渗透率.该研究为制备符合PEMFC使用条件的氢气提供了可靠依据,同时为综合利用煤层气提供了新的途径。 相似文献
34.
用B3LYP/6 31 1 + +G 方法研究了H2 S与HO2 自由基之间的氢键。发现了三个能量极小点。同时做了H2 S·HO2 的振动频率分析。计算预测了能量整体最小点的构型为带有 2个扭曲的氢键的五元环结构 相似文献
35.
The present study examines the behavior of a classical charged point particle in near-elliptic orbits about an infinitely massive and oppositely charged nucleus, while acted upon by applied electromagnetic radiation. As recently shown for near-circular orbits, and now extended here to the elliptical case, rather surprising nonlinear dynamical effects are readily produced for this simple system. A broad range of stability-like conditions can be achieved by applying radiation to this classical atom. A perfect balance condition is examined, which requires an infinite number of plane waves representing harmonics of the orbital motion. By applying a scale factor to this radiation, stability-like conditions are produced where periodic variations in semimajor and semiminor axes occur for extended periods of time, before orbital decay eventually takes over due to the effects of radiation reaction. This work is expected to lead to both practical suggestions on experimental ideas involving controlling ionization and stabilization conditions, as well as hopefully aiding in theoretical explorations of stochastic electrodynamics. 相似文献
36.
Scanning electron microscope (SEM) tribometric data on polycrystalline silicon (poly-Si) vs. poly-Si, Si(100) vs. Si(100)
and Si(111) vs. Si(111) interfaces, obtained in
Torr and in 0.2 Torr partial pressure of hydrogen gas (
) from room temperature to 850°C, were performed under standard and much slower thermal ramping rates. The friction data were analyzed per the methodology
described in part I of this paper series. The results indicate a highly beneficial friction- and wear-reducing regime within
a relatively narrow thermal region. This desirable region coincides with some chemisorption of excited species of molecular
hydrogen just before the mass thermal desorption of surface hydrides. These data represent the tribochemical equivalent of
a method routinely used in electronics, whereby deep electron traps (dangling Si bonds) are passivated by baking in molecular
hydrogen. The
also exerts a moderating influence on the size of the friction noise at all test temperatures. However, the general level
of friction beyond the beneficial thermal region is high. In parallel, the general wear rate of Si representative of the entire
range of standard thermal ramping in both atmospheric environments is in the extremely high 10-12m3/(N m) range. Operating strictly in the beneficial, low-friction thermal regime resulted in a several orders-of-magnitude
reduction in the wear rate over those measured under standard thermal ramping conditions. Although the results confirm previous
findings that Si is not a good material of construction for miniaturized moving mechanical assemblies (e.g., microbearings
and gears), there seems to be some limited possibility of gas-phase lubrication of Si micromechanisms with rarefied hydrogen
at surface temperatures between 100 and 300°C.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
37.
为了强化甲醇制氢反应,分别以酚醛树脂和间苯二酚-甲醛为前驱体,制备了炭膜及复合炭膜.采用扫描电镜和氮气物理吸附等手段对炭膜及复合炭膜的微观形貌与孔径分布进行了分析.考察了原料粒度及固化剂用量对炭膜孔结构以及涂膜次数对复合膜分离性能的影响,并将所制备的炭膜与复合炭膜耦合在反应器内用于强化甲醇水蒸汽重整制氢反应.结果表明,当固化剂质量分数为6%时,炭膜孔径分布最窄,且平均孔径为0.16μm.随涂膜次数从1次增至3次,复合炭膜的透气性先降低后增大.对于甲醇水蒸汽重整制氢反应的转化率而言,炭膜与复合炭膜反应器分别比传统固定床提高了1.6倍和1.9倍. 相似文献
38.
Lithium Intercalation Compound Dramatically Influences the Electrochemical Properties of Exfoliated MoS2 下载免费PDF全文
Adriano Ambrosi Zdeněk Sofer Martin Pumera 《Small (Weinheim an der Bergstrasse, Germany)》2015,11(5):605-612
MoS2 and other transition metal dichalcogenides (TMDs) have recently gained a renewed interest due to the interesting electronic, catalytic, and mechanical properties which they possess when down‐sized to single or few layer sheets. Exfoliation of the bulk multilayer structure can be achieved by a preliminary chemical Li intercalation followed by the exfoliation due to the reaction of Li with water. Organolithium compounds are generally adopted for the Li intercalation with n‐butyllithium (n‐Bu‐Li) being the most common. Here, the use of three different organolithium compounds are investigated and compared, i.e., methyllithium (Me‐Li), n‐butyllithium (n‐Bu‐Li) and tert‐butyllithium (t‐Bu‐Li), used for the exfoliation of bulk MoS2. Scanning transmission electron microscopy (STEM), Raman spectroscopy, X‐ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV) are adopted for a comprehensive characterization of all materials under investigation. In addition, catalytic properties towards the hydrogen evolution reaction (HER) and capacitive properties are also tested. Different organolithium compounds exhibit different extent of Li intercalation resulting in different degrees of exfoliation. The inherent electrochemical behavior of MoS2 consisting of significant anodic and cathodic peaks as well as its capacitive behavior and catalytic properties towards hydrogen evolution reaction are strongly connected to the exfoliation compound used. This research significantly contributes to the development of large‐scale synthesis of electrocatalytic MoS2‐based materials. 相似文献
39.
A novel biosensor based on a myoglobin/gold nanoparticles/carbon spheres (Mb-AuNPs-CNs) 3-D architecture bioconjunction has
been fabricated for the determination of hydrogen peroxide (H2O2). Cyclic voltammetry (CV), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM) were used
to characterize the bioconjunction of the AuNPs-CNs with Mb. Experimental results demonstrate that the AuNPs-CNs hybrid material
is more effective in facilitating electron transfer of the immobilized enzyme than CNs alone, which can be attributed to the
unique nanostructure and larger surface area of the bioconjunction. The biosensor displayed good performance for the detection
of H2O2 with a wide linear range from 0.28 μmol/L to 116.5 μmol/L and a detection limit of 0.12 μmol/L. The Michaelis-Menten constant
K
Mapp value was estimated to be 0.3 mmol/L. The resulting biosensor exhibited fast amperometric response, and good stability, reproducibility,
and selectivity to H2O2.
This article is published with open access at Springerlink.com 相似文献
40.