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31.
32.
In order to study the dehydrogenation of ethylbenzene to styrene, epitaxial iron oxide model catalyst films with Fe3O4(111), -Fe2O3(0001) and KFe
x
O
y
(111) stoichiometry were prepared in single crystal quality on Pt(111). They were investigated using surface science techniques before and after atmospheric pressure reaction experiments in a newly designed single crystal flow reactor. As expected from low-pressure measurements, Fe3O4(111) is catalytically inactive. The catalytic activity of -Fe2O3(0001) starts after an activation period of about 45 min. After that, the surface is essentially clean but shows a high concentration of defects. On the potassium-promoted films, however, the activation period is much longer, the activity then is higher and the surface gets covered completely with carbon and oxygen during reaction. This indicates a different reaction pathway on the promoted films with a carbon–oxygen species as catalytically active species. 相似文献
33.
In the field of biomaterials and biomedical devices, surface activation has been focused on creating functional groups capable of preferential adsorption of biologically active species (proteins, enzymes, cells, drugs, etc.). In this way an interface can be created between the synthetic material and the biological medium, with the aim of increasing the compatibility of the implant with the human organism. In our experiments a dielectric barrier discharge (DBD), in helium at atmospheric pressure, was used as the source of energy capable of creating active centers that render the functionalized surface favorable to immobilization of biological molecules. Retention of immunoglobulin (IgG) and heparin biomolecules on polyamide‐6 (PA‐6) surfaces after treatment by the DBD was analyzed by atomic force microscopy, adhesion evaluation, and measurement of the contact angle titration in order to assess this incorporation on the treated surfaces. The marked adsorption of the biomolecules on the active sites created by DBD on the exposed surfaces also was related to a complex set of processes, such as enhanced roughness, increased surface wettability, and modified distribution of cationic and anionic groups on the treated surfaces. All these factors could promote interfacial interactions between the specific groups of the biomolecules existing in the biological medium and the type of cationic and/or anionic groups present on the surface. The efficiency of the DBD treatment showed that the DBD technique is useful for preactivation of the polymer surface for immobilization of other biologically active species (such as drugs and enzymes). © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1985–1990, 2003 相似文献
34.
A.J. Dickinson L.P.L. Carrette J.A. Collins K.A. Friedrich U. Stimming 《Journal of Applied Electrochemistry》2004,34(10):975-980
This paper describes the effects of varying the Pt to Ru ratio in carbon-supported catalysts for methanol oxidation as a function of temperature. Previously these effects were studied in isolation, but now it is shown that the composition of a given catalyst as a function of temperature is extremely important for its activity towards methanol oxidation. Platinum rich 3:2 atomic ratio catalysts perform better than a 1:1 catalyst at 25 °C, where only Pt is believed to be active towards methanol dehydrogenation, since this process is a highly thermally activated process on Ru sites. This result is reversed at 65 °C, where the 1:1 catalyst displays much higher currents across the entire range of polarization. This may result from methanol dehydrogenation occurring on both Ru and Pt sites at higher temperatures. At an intermediate temperature, 45 °C, the 3:2 catalyst is seen to perform better at lower current values, while the 1:1 catalyst is superior at higher current densities, with the crossover occurring at 62 A g–1. As a consequence, when designing fuel cell catalysts, the composition of the catalyst employed should be tailored with respect to the exact operating conditions, in order to promote optimum fuel cell performance. 相似文献
35.
36.
The free‐radical graft polymerization of vinyl acetate onto nonporous silica particles was studied experimentally. The grafting procedure consisted of surface activation with vinyltrimethoxysilane, followed by free‐radical graft polymerization of vinyl acetate in ethyl acetate with 2,2′‐azobis(2,4‐dimethylpentanenitrile) initiator. Initial monomer concentration was varied from 10 to 40% by volume and the reaction was spanned from 50 to 70°C. The resulting grafted polymer, which was stable over a wide range of pH levels, consisted of polymer chains that are terminally and covalently bonded to the silica substrate. The experimental polymerization rate order, with respect to monomer concentration, ranged from 1.61 to 2.00, consistent with the kinetic order for the high polymerization regime. The corresponding rate order for polymer grafting varied from 1.24 to 1.43. The polymer graft yield increased with both initial monomer concentration and reaction temperature, and the polymer‐grafted surface became more hydrophobic with increasing polymer graft yield. The present study suggests that a denser grafted polymer phase of shorter chains was created upon increasing temperature. On the other hand, both polymer chain length and polymer graft density increased with initial monomer concentration. Atomic force microscopy–determined topology of the polymer‐grafted surface revealed a distribution of surface clusters and surface elevations consistent with the expected broad molecular‐weight distribution for free‐radical polymerization. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 300–310, 2003 相似文献
37.
黄坚萍 《化学推进剂与高分子材料》2007,5(4):57-59
运用钽平台石墨管测定基体成分复杂的废水样品中的Cd、Pb元素,基本消除了基体残留影响和记忆效应,降低了背景吸收,提高了灵敏度。样品经超声波仪粉碎后直接进样,用校正曲线法测定,简化了操作步骤,减少了测定时间,延长了石墨管使用寿命。其测定值与石墨平台标准加入法测定值结果一致。样品回收率:Cd为96.9%~104%,Pb为98.2%~106%,Cd的相对标准偏差(RSD)为3.04%~4.24%,Pb的RSD为2.93%~6.53%。 相似文献
38.
裴勇 《数字社区&智能家居》2014,(12):8221-8222
在我国数字化教学资源建设领域,建设微型教学资源受到了广泛的关注。建设职业教育微型教学资源时,因工作过程知识类别多、情境多样、注重实践等特点,使资源建设存在一定的难度。分析工作任务的关联逻辑,借助工作流技术对工作流程建模,划分最小粒度的原子任务,并通过分析原子任务工作过程知识的要素组织逻辑,设计资源的框架结构,为职业教育"微"资源建设提供了更具操作性的方法。 相似文献
39.
The initial rate of colloid deposition onto semi‐permeable membranes is largely controlled by the coupled influence of permeation drag and particle‐membrane colloidal interactions. Recent studies show that the particle‐membrane interactions are subject to immense local variations due to the inherent morphological heterogeneity (roughness) of reverse osmosis (RO) and nanofiltration (NF) membranes. This experimental investigation reports the effect of membrane roughness on the initial deposition of polystyrene latex particles on a rough NF membrane during cross flow membrane filtration under different operating pressures and solution chemistries. Atomic force microscopy was used to characterize the roughness of the membrane and observe the structure of particle deposits. At the initial stages of fouling, the AFM images show that more particles preferentially accumulate near the “peaks” than in the “valleys” of the rough NF membrane surface. 相似文献
40.