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排序方式: 共有1483条查询结果,搜索用时 15 毫秒
1.
介绍了高可靠电镀Ni/Au工艺在PTFE微波印制电路上的应用,并分析了氨基磺酸盐镀软镍和亚硫酸盐镀软金工艺的影响因素及提高Ni/Au镀层之间附着力的措施。通过实验及应用证明了与直接镀金工艺相比,在软基材PTFE敷铜箔板上镀Ni/Au工艺能大大提高微波电路的可焊性,高温稳定性和长期可靠性,并且用其所制作的微波器件的高频性能也优于直接镀金工业。 相似文献
2.
The relatively fast diffusion of Au atoms in eutectic PbSn matrix is considered one of the contributing factors to the Au
embrittlement problem. In this study, we further investigated the Au embrittlement problem in high-Sn solders. Experimentally,
Sn3.5Ag (wt.%) spheres with 500-μm diameter were soldered over the Au/Ni soldering pads. It was found that some of the AuSn4 needles that formed after reflow inside the solder migrated back to the solder/pad interface during thermal aging. However,
the migration kinetics in high-Sn solders was slower compared to that in eutectic PbSn. The difference in migration kinetics
of AuSn4 in eutectic PbSn and SnAg was ascribed to the difference in the magnitudes of the Au flux and the Ni flux. In eutectic PbSn,
the Au flux was much greater than that of the Ni flux, and the Au and Ni flux were in the same order of magnitude in eutectic
SnAg. The relative magnitude of the Au and Ni flux changed in eutectic PbSn and SnAg because the homologous temperatures of
PbSn and SnAg were different. 相似文献
3.
Benedetto Bozzini Bertrand Busson Claudio Mele Abderrahmane Tadjeddine 《Journal of Applied Electrochemistry》2008,38(7):897-906
We report on potential-dependent in situ SFG and DFG spectroscopy carried out at Au(111), Au(210), polycrystalline Au, Au–Cu
and Au–Ag–Cu electrodes in contact with aqueous solutions containing CN− and 4-cyanopyridine (4CP). Spectroelectrochemical work was complemented by cyclic voltammetry. The chief stress has been
placed on systematising and quantifying the interaction between 4CP and CN− and the attending effects on the vibrational and electronic structures of the interface. The voltammetric behaviour of the
investigated electrodes, modified by the addition of 4CP to the CN− electrolyte, denote changes in the CN− adsorption characteristics and effects of the adsorbed CN− layer on the electrodic reactivity of 4CP. The differences among the investigated electrodes can be explained in terms of
their respective degrees of atomic packing or with alloying effects on the stability of adsorbed CN−. The potential-dependent spectra have been analysed quantitatively with a model for the second order non linear susceptibility
accounting for vibrational and electronic effects. The spectral changes induced by addition of 4CP denote interaction of the
aromatic with the electrode through the CN− monolayer. The non-resonant contribution yields information on the effects of 4CP on the fine structure of the bound electron
density of states. 相似文献
4.
贵金属Cu、Ag、Au的电子结构和物理性质 总被引:1,自引:0,他引:1
由纯金属单原子理论(OA)确定了面心立方结构(FCC)贵金属Cu、Ag、Au的电子结构依次为[Ar](3dn)5.58(3dc)4.21(4sc)0.23(4sf)0.98、[Kr](4dn)4.87(4dc)4.56(5sc)0.66(5sf)0.91、[Xe](5dn)4.20(5dc)4.90(6sc)1.57(6sf)0.33,并确定了Cu、Ag、Au的密排六方结构(HCP)和体心立方结构(BCC)两种初态特征晶体和初态液体的电子结构。根据自然态的电子结构定性解释了熔点、拉伸强度、维氏硬度、体弹性模量、电导和热导率物理性质差异与电子结构的关系,定量计算了晶格常数、结合能、势能曲线及线热膨胀系数随温度的变化。根据非自然态的电子结构,定性解释了晶体结构BCC和HCP的关系。 相似文献
5.
Hydrogen evolution during formaldehyde oxidation in alkaline solution has been monitored by Differential Electrochemical Mass Spectrometry on Au(111) and polycrystalline gold. The current efficiency for hydrogen evolution increases with higher concentration and is in the same range on both, polycrystalline Au and Au(111) electrode. The onset potentials and half-wave potentials are higher on Au(111). Reaction orders for the faradaic current on the bare gold electrodes have been determined as 0.21 for higher and 0.76 for lower concentrations. Reaction orders for hydrogen evolution during formaldehyde oxidation are 1.4 times higher in each case. Tafel slopes in the range of 140-160 mV are found. This signifies that the first reaction step involving the formation of adsorbed hydrogen is largely determining the overall reaction rate. In the presence of thallium adlayers hydrogen evolution from formaldehyde oxidation is largely suppressed. On the thallium modified polycrystalline Au, formaldehyde oxidation is shifted for 100 mV to higher potentials where Tl is partially desorbed and hydroxide is coadsorbed on the modified surface. On thallium modified Au(111), a similar process takes place, but in the same potential region as the onset of formaldehyde oxidation on the bare surface and therefore the formaldehyde oxidation is only slightly shifted. Tafel slopes are decreased to 80 mV/dec in the presence of thallium. In the presence of adsorbed thallium, the first reaction step is in equilibrium, the coverage with adsorbed hydrogen is smaller and its recombination to H2 is largely suppressed. 相似文献
6.
K. Juodkazis J. Juodkazyt? T. Juodien? V. Šukien? I. Savickaja 《Electrochimica acta》2006,51(27):6159-6164
The idea of underpotential oxidation of water, taking place on the surface of noble metals in the range of potentials preceding molecular oxygen evolution, is more than 40-years old. Chemisorbed oxygen atom—Ochem is considered to be the main intermediate in the underpotential oxidation of H2O, leading eventually to chemical oxidation of noble metals and formation of anhydrous surface oxides of MeO type. This concept is still used for the evaluation of the real surface area of the noble metal electrodes and also for the interpretation of new experimental results.The existence of reversible metal-oxide electrodes demonstrated experimentally for Pt, Pd, Rh, Ir and Au electrodes, oxidized anodically in the range of potentials preceding O2 evolution, shows that noble metals do have electrochemistry of their own. Nanometric layers of amorphous, slightly soluble hydroxides, hydrous oxides or oxides can form electrochemically on the electrode surface during the anodic process and be reduced during the cathodic one. Such alternative concept admits the reversibility of anodic and cathodic processes and changes essentially the understanding and interpretation of the phenomena of anodic oxidation of noble metals. 相似文献
7.
8.
Masashi Shou Hiroyuki Takekawa Dong-Ying Ju Tokio Hagiwara Da-ling Lu Ken-ichi Tanaka 《Catalysis Letters》2006,108(3-4):119-124
Catalytic activity of a 1 wt% Au/TiO2 catalyst is markedly improved by loading a large amount of FeOx, on which the oxidation of CO in excess H2 is selectively promoted at temperature lower than 60 °C. Oxidation of CO with O2 on the FeOx/Au/TiO2 catalyst is markedly enhanced by H2, and H2O moisture also enhances the oxidation of CO but its effect is not so large as the promotion by H2. We deduced that activation of Au/TiO2 catalyst by loading FeOx is not caused by the size effect of Au particles but a new reaction path via hydroxyl carbonyl intermediate is responsible
for the superior activity of the FeOx/Au/TiO2 catalyst. 相似文献
9.
Abdullahi Nuhu Jorge Soares Monica Gonzalez-Herrera Andrew Watts Ghulam Hussein Michael Bowker 《Topics in Catalysis》2007,44(1-2):293-297
We have investigated the adsorption and reaction of methanol with Au/TiO2 catalysts using a pulsed flow reactor, DRIFTS and TPD. The TiO2 (P25) surface adsorbed a full monolayer of methanol, much of it in a dissociative manner, forming methoxy groups associated
with the cationic sites, and hydroxyl groups at the anions. The methoxy is relatively stable until 250 °C, at which point
decomposition occurs, producing mainly dimethyl ether by a bimolecular surface reaction. As the concentration of methoxy on
the surface diminishes, so the mechanism reverts to a de-oxygenation pathway, producing mainly methane and water (at ~330 °C
in TPD), but also with some coincident CO and hydrogen. Au catalysts were prepared by the deposition-precipitation method
to give Au loadings between 0.5–3 wt %. The effect of low levels of Au on the reactivity is marked. The pathway which gives
methane, which is characteristic of titania, remains, but a new feature of the reaction is the evolution of CO2 and H2 at lower temperature (a peak is seen in TPD at 220 °C), and the elimination of the DME-producing state. Clearly this is associated
with the presence of Au and appears to be due to the production of a formate species on the surface of the Au component. This
formate species is mainly involved in the reaction of methanol with the Au/TiO2 catalysts which results in a combustion pathway being followed, with complete conversion occurring by ~130 °C. 相似文献
10.
Inductive high-frequency impedance behaviour is often observed in metal electrodeposition systems. This behaviour is typically attributed to equipment limitations or non-idealities in the cell set-up and electrical connections. Such instrumental artefacts would nevertheless be relevant to a frequency range which is expected to be well above that in which inductive behaviour is in fact observed (down to a few tens of Hz). In this paper some results on an acidic Au—Sn electrodeposition system are reported. Electrochemical impedance and potentiostatic transients were measured. These results suggest that the high-frequency inductive behaviour may be related to metal nucleation processes. A correlation is proposed between the pseudo-inductive potentiostatic nucleation transients and the pseudo-inductive behaviour of the impedance spectra. 相似文献