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1.
In this study, the destabilization resistance of Sc2O3 and CeO2 co-stabilized ZrO2 (SCZ) ceramics was tested in Na2SO4 + V2O5 molten salts at 750°C–1100 °C. The phase structure and microstructure evolution of the samples during the hot corrosion testing were analyzed with X-ray diffraction (XRD), Raman spectra, scanning electron microscopy (SEM), energy dispersive X-ray spectrum (EDS), and X-ray photoelectron spectroscopy (XPS). Results showed that the destabilization of SCZ ceramics at 750 °C was the result of the chemical reaction with V2O5 to produce m-ZrO2 and CeVO4, and little ScVO4 was detected in the Sc2O3-rich SCZ ceramics. The primary corrosion products at 900 °C and 1100 °C were CeO2 and m-ZrO2 due to the mineralization effect. The Sc2O3-rich SCZ ceramics exhibited excellent degradation resistance and phase stability owing to the enhanced bond strength and the decreased size misfit between Zr4+ and Sc3+. The destabilization mechanism of SCZ ceramic under hot corrosion was also discussed.  相似文献   
2.
Owing to the good physicochemical compatibility and complementary mechanical properties of Ti3SiC2 and Al2O3, Ti3SiC2/Al2O3 composites are considered as ideal structural materials. However, TiC and TiSi2 typically coexist during the synthesis of Ti3SiC2/Al2O3 composites through an in-situ reaction, which adversely affects the mechanical properties of the resulting composites. In this study, Ti3SiC2/Al2O3 composites were prepared via in-situ hot pressing sintering at 1450 °C. Ge, which was used as a sintering aid, improved the purity and mechanical properties of the Ti3SiC2/Al2O3 composites. This is because Ge replaced some of the Si atoms to compensate the evaporation loss of Si to form Ti3(Si1-xGex)C2, which showed a crystal structure similar to that of Ti3SiC2. Furthermore, the molten Ge accelerated the diffusion reaction of the raw materials, increasing the overall density of the Ti3SiC2/Al2O3 composites. The optimum Ge amount for improving the mechanical properties of the composites was found to be 0.3 mol. The flexural strength, fracture toughness, and microhardness of the composite with the optimum Ge amount were 640.2 MPa, 6.57 MPa m1/2, and 16.21 GPa, respectively. The formation of Ti3(Si1-xGex)C2 was confirmed by carrying out X-ray diffraction, energy dispersive spectroscopy, and transmission electron microscopy analyses. A model crystal structure of Ti3(Si1-xGex)C2 doped with 0.3 mol Ge was established by calculating the solid solubility of Ge.  相似文献   
3.
为避免传统均匀采样方法因忽视曲线重要特征而生成不理想的采样结果,获得给定数量且由特征点和辅助点组成的采样点序列,提出基于特征识别的高质量空间曲线非均匀采样方法.首先使用抛物线插值法得到曲线上所有曲率极大值点和挠率极大值点的近似位置,经筛选后产生特征点,以更好地抓住空间曲线的轮廓特征.然后定义基于弧长、曲率和挠率加权组合的特征函数,并以此自适应地选取曲线上的辅助点.与3种主流采样方法比较的实验结果表明,该方法能够获得更高质量的采样结果且具有更好的实用性,从而进一步改善空间曲线的B样条拟合效果.  相似文献   
4.
《Ceramics International》2021,47(18):25689-25695
The high-temperature mechanical and dielectric properties of Si2N2O ceramics are often limited by the introduction of a sintering aid. Herein, dense Si2N2O was prepared at 1700 °C by hot-pressing oxidized amorphous Si3N4 powder without sintering additives. A homogeneous network with short-range order and a SiN3O structure was formed in the oxidized amorphous Si3N4 powder during the hot-pressing process. Si2N2O crystals preferentially nucleated at positions within the SiN3O structure and grew into rod-like and plate-like grains. Fully dense ceramics with mainly crystalline Si2N2O and some residual amorphous phases were obtained. The as-prepared Si2N2O possessed a good flexural strength of 311 ± 14.9 MPa at 1400 °C, oxidation resistance at 1500 °C, and a low dielectric loss tangent of less than 5 × 10−3 at 1000 °C.  相似文献   
5.
A bulk (Hf0.2Ta0.2Zr0.2Nb0.2Ti0.2)C high-entropy ceramic (HEC) with a high density was prepared by hot pressing (HP), and through a robust joining technique, large-sized piece was fabricated. A hot-pressed carbide HEC with a single-phase and homogeneous composition was obtained at the sintering temperatures from 1800 to 1950 °C for 30 min under a pressure of 30 MPa. The influence of sintering temperature on the mechanical properties of the HEC was investigated, and the flexural and compressive strengths were reported. Additionally, the feasibility of active brazing of this HEC was studied and solid joints with high shear strength were obtained by atomic diffusion and chemical reaction at the interface, providing a key approach to fabricate complex components of HECs.  相似文献   
6.
Targeting higher toughness transparent ceramics, tetragonal (3 mol % yttria) and cubic (8 mol % yttria) ZrO2 starting powder mixtures were densified by spark plasma sintering (SPS) in vacuum at 1100 °C and post hot isostatic pressing (HIP) in argon at 1100 °C. The influence of the ultra-fine microstructure and phase composition on the fracture resistance and light transmission in the visible and infra-red range was assessed. Of special interest was the influence of a thermal annealing step in air on the transparency of the SPS and SPS-HIP ceramics.  相似文献   
7.
Graphite–SiC micro-composites have been prepared in–house by carbothermal reduction process. Controlling the process parameters including the weight ratio of SiO2 to graphite as well as carbothermal reduction temperature during the micro-composite preparation favors the homogeneous formation of SiC with preferred morphologies like ribbons and whiskers/fibers. The micro-composite modified low carbon MgO-C refractories have exhibited significantly improved bulk properties over the standard composition. To understand the beneficial role of SiC reinforcement on hot strength performance under air oxidizing conditions, we propose a scaling parameter known as strength factor (fs) based on the ratio of hot strength (HMOR) to cold strength (CCS). Correlating the strength factor data (fs) with oxidative damage provides new insights into the reinforcing effects of distinct SiC morphologies in this new class of micro-composite fortified refractory systems over the standard compositions.  相似文献   
8.
Yb3+-doped Lu2O3 nanoparticles produced by laser ablation were used to fabricate transparent ceramics by a combination of pressureless sintering in vacuum (PS) followed by a hot isostatic pressing (HIPing). The samples were subjected to various PS and HIPing conditions and the microstructure evolution and its correlation with the transmittance were investigated. Relative densities of over 97% were achieved after PS at the temperatures of 1250–1700 °C. Rapid grain growth occurred within PS and HIPing temperatures above 1500 °C leading to formation of intragranular porosity which is deleterious for optical quality. Higher transmittance (81.7% at λ = 1080 nm) and ultrafine microstructure with an average grain size of 0.35 μm were obtained by PS at 1250 °C followed by HIPing at 1400 °C for 5 h under 207 MPa. Output power of 2.02 W with a slope efficiency of 46.5% was obtained under a quasi-continuous wave end pumping at 929.4 nm.  相似文献   
9.
《Ceramics International》2022,48(11):15364-15370
This study reports on the preparation and mechanical properties of a novel SiCnf/SiC composite. The single crystal SiC nanofiber(SiCnf) reinforced SiC ceramic matrix composites (CMC) were successfully fabricated by hot pressing the mixture of β-SiC powders, SiCnf and Al–B–C powder. The effects of SiCnf mass fraction as well as the hot-pressing temperature on the microstructure and mechanical properties of SiCnf/SiC CMC were systematically investigated. The results demonstrated that the 15 wt% SiCnf/SiC CMC obtained by hot pressing (HP) at 1850 °C with 30 MPa for 60 min possessed the maximum flexural strength and fracture toughness of 678.2 MPa and 8.33 MPa m1/2, respectively. The nanofibers pull out, nanofibers bridging and cracks deflection were found by scanning electron microscopy, which are believed can strengthen and toughen the SiCnf/SiC CMC via consuming plenty of the fracture energy. Besides, although the relative density of the prepared SiCnf/SiC CMC further increased with the sintering temperature rose to 1900 °C, the further coarsend composites grains results in the deterioration of the mechanical properties for the obtained composites compared to 1850 °C.  相似文献   
10.
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