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991.
A simple and efficient activation process was conducted by deposition of palladium (Pd) nanoparticles on PMMA surface using a microwave-assisted polyol method with ethanol used as the reductant. The newly synthesized Pd nanoparticles were utilized as an activator for electroless nickel deposition. TEM images revealed that Pd nanoparticles of size 4-6 nm are formed evenly over the PMMA surface. A tight, smooth and continuous Ni plating layer was coated on these Pd nanoparticle activated PMMA microspheres. In contrast, a rough and discontinuous Ni film was obtained for the sample activated with a conventional sensitization/activation procedure. 相似文献
992.
Hexagonal ZnIn2S4 porous microspheres were synthesized via a cetylpyridinium bromide (CPBr)-assisted hydrothermal method. The structure, morphology and optical property of these prepared products were characterized by wide angle X-ray diffraction (WAXRD), small angle X-ray diffraction (SAXRD), UV-Vis diffusive reflectance spectroscopy (DRS), field emission scanning electron microscopy (FESEM), energy dispersive X-ray analyzer (EDX) and nitrogen sorption analysis. The effects of CPBr and pH on the crystal structure, morphology and photocatalytic activity of ZnIn2S4 products were studied. The results demonstrated that the flowerlike ZnIn2S4 microspheres, which were composed of numerous nanosheets, performed higher visible-light photocatalytic activity than bulk ZnIn2S4 for hydrogen evolution. The CPBr addition influenced the crystal structure including the position and intensity of some peaks. Furthermore, the pH played a crucial role in the formation of ZnIn2S4 porous microspheres. The as-synthesized porous ZnIn2S4 microspheres possessed the specific surface area of 165.4 m2 g−1 and the slit-like porous configuration, which was beneficial to photocatalytic reaction. 相似文献
993.
Well dispersed Fe3O4 nanoparticles with mean size about 160 nm are synthesized by a simple chemical method at atmosphere pressure. The products are characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and Raman spectrum. Electrochemical properties of the as-synthesized Fe3O4 nanoparticles as anode electrodes of lithium ion batteries are studied by conventional charge/discharge tests, showing initial discharge and charge capacities of 1140 mAh g−1 and 1038 mAh g−1 at a current density of 0.1 mA cm−2. The charge and discharge capacities of Fe3O4 electrode decrease along with the increase of cycle number, arriving at minimum values near the 70th cycle. After that, the discharge and charge capacities of Fe3O4 electrode begin to increase along with the increase of cycle number, arriving at 791 and 799 mAh g−1 after 393 cycles. The morphology and size of the electrode after charge and discharge tests are characterized by SEM, which exhibits a large number of dispersive particles with mean size about 150 nm. 相似文献
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996.
采用溶液聚合法合成了PEG-IPDI-DMPA嵌段离聚体,通过FTIR、1H-NMR、GPC、DSC、TEM对其结构进行了表征;并通过粒径、比浓粘度、旋转粘度和电导率,对其在水相中的溶液行为进行了研究。红外光谱分析证实,合成获得了预期的聚氨酯结构嵌段离聚体;差示扫描量热分析证明,离聚体分子链段是由硬段和软段两相组成的嵌段共聚物;经透射电镜观察,嵌段离聚体在水溶液中呈现出较为规整的球形粒子状态。PEG-IPDI-DMPA嵌段离聚体粒径都在200nm左右;PEG-IPDI-DMPA嵌段离聚体是剪切变稀的。 相似文献
997.
采用高温固相两步法制备了两种Li1.4M0.4Ti1.6(PO4)3(M=Al、Cr)系列NASICON功能材料,对不同掺杂合成的样品进行了XRD和SEM表征,并分别对其Na+的交换吸附容量进行了测定。结果表明,对LiTi2(PO4)3掺入适量的Al3+和Cr3+后未改变其晶体结构,合成的吸附剂粒径分布在5~10μm;Li1.4M0.4Ti1.6(PO4)3(M=Al、Cr)对Na+有特效吸附作用,当pH=11.0时,Li1.4Al0.2Cr0.2Ti1.6(PO4)3的饱和交换吸附容量可达69.26mg/g。 相似文献
998.
Ting Yu Julian Oppermann Chris Bradley Oliver Sinnen 《Concurrency and Computation》2016,28(5):1480-1506
Biomedical modelling that is mathematically described by ordinary differential equations (ODEs) is often one of the most computationally intensive parts of simulations. With high inherent parallelism, hardware acceleration based on field programmable gate array has great potential to increase the computational performance of the ODE model integration while being very power efficient. ODE‐based Domain‐specific Synthesis Tool is a tool we proposed previously to automatically generate the complete hardware/software co‐design framework for computing biomedical models based on CellML. Although it provides remarkable performance improvement and high energy efficiency compared with CPUs and GPUs, there is still a great potential for optimisation. In this paper, we investigate a set of optimisation strategies including compiler optimisation, resource fitting and balancing, and multiple pipelines. They all have in common that they can be performed automatically and hence can be integrated in our domain‐specific high level synthesis tool. We evaluate the optimised hardware accelerator modules generated by ODE‐based Domain‐specific Synthesis Tool on real hardware based on their resource usage, processing speed and power consumption. The results are compared with single threaded and multi‐core CPUs with/without Streaming SIMD Extension (SSE) optimisation and a graphics card. The results show that the proposed optimisation strategies provide significant performance improvement and result in even more energy‐efficient hardware accelerator modules. Furthermore, the resources of the target field programmable gate array device can be more efficiently utilised in order to fit larger biomedical models than before. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
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采用等体积浸渍法制备了系列不同MgO含量的CuO-Bi2O3-MgO/γ-Al2O3催化剂,用N2-BET、XRD和TPR对其进行表征,并考察了其催化甲醛溶液和乙炔合成1,4-丁炔二醇的性能。结果表明,添加适量的MgO可显著改进催化剂的活性和选择性,其中γ-Al2O3先负载质量分数1%的MgO,700℃焙烧后,再共浸渍CuO和Bi2O3后500℃焙烧制备的30%CuO-2%Bi2O3-1%MgO/γ-Al2O3催化剂性能较好,1,4-丁炔二醇产率和选择性可分别达到67.9%和90.3%。 相似文献