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1.
本文在环氧涂料中添加玄武岩鳞片,提高其防腐蚀性能。针对玄武岩鳞片的团聚问题,通过机械力化学改性工艺,采用正硅酸四乙酯、HY-311型钛酸酯偶联剂、E-44型环氧树脂对玄武岩鳞片进行杂化包覆,结果表明,杂化包覆后玄武岩鳞片的沉降时间从2h提高至96 h。杂化包覆玄武岩鳞片添加量为20%涂层的性能最优,附着力为13.40 MPa,耐盐雾时间为2000 h,在3.5%NaCl溶液中浸泡2000 h后,0.01 Hz的阻抗模值仍然有5.15×109 Ω·cm2。  相似文献   
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采用微波消解法和石墨消解法对土壤样品进行预处理,用火焰原子吸收分光光度法测定土壤中铜和锌的含量。对3个土壤标准物质(GSS-17、GSS-30、GSS-34)的精密度和准确度进行了分析,结果表明:微波消解法和石墨消解法的检出限、精密度和准确度均能满足土壤检测的要求,石墨消解法相对于微波消解法更加便捷,具有很好的精密度和准确度。  相似文献   
4.
Commodity polymers are the most widely used materials for electronic packaging applications. However, they are nondegradable and causing serious environmental damage. Addressing this challenge, the relative effects of graphite (G) and graphene oxide (GO) dispersion on the enzymatic degradation, electronic properties, thermal degradation, and crystallization behavior of enzyme degradable polylactide/poly(ε-caprolactone) blend composites is investigated. Owing to the oxygenated surface functionalities and excellent thermal conductivity arising from the carbon structure, the randomly dispersed GO particles do not provide electrical pathways and facilitate large enhancements in the electrical resistivity (126%) and thermal conductivity (72%) of the blend composites. However, while the G particles enhanced the thermal conductivity of the composites, they had little effect on enzymatic degradation. Furthermore, they reduced the electrical resistivity, particularly at high concentration (0.25 wt % G), as a result of the conducting delocalized electrons in the G structure and due to network formation. We also find that the energy required to initiate and propagate the thermal degradation process for GO-filled blend composites is relatively lower than that of G-filled blend composite. However, the former composites show higher crystallization rate coefficients value than that of G-filled composites and the neat blend, thereby providing better crystallization ability and miscibility with the matrix. In summary, the GO-filled blend composites are observed to show potential for use in sustainable materials for thermal management applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47387.  相似文献   
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The present work aims to present the results based on the processing of nanocomposites, which consist of matrix materials like epoxy and filler materials such as conjugated nanomaterials/allotropes of carbon, namely, carbon black, graphite, and multiwalled carbon nanotube (MWCNT) used for targeted applications. To improve the physical and chemical properties and to facilitate a better interfacial interface between the polymer and nanotube, functional MWCNT is used during the preparation of the composite. The prime objective of the study is to establish the thermal, mechanical, and electrical properties of nanocomposites using experimental methods. It has been observed from the experimental results that carbon nanotube (CNT) based composite exhibits higher mechanical (tensile and hardness) and thermal properties as compared with the others. The electrical properties are found to be better in a graphite-based composite. Although CNT has superior mechanical and thermal properties, the exorbitant price limits its use. Hence, the allotropes of carbon may be used judiciously considering both the cost and property requirements of the targeted application. The work also studies the dispersion state of nanofibers through scanning electron microscopy (SEM).  相似文献   
6.
废弃锂离子电池的负极活性材料主要为石墨,现阶段对于废弃锂离子电池中的石墨主要采用填埋等方法进行处理,造成了资源的浪费和环境的污染。现有的研究表明,废弃锂离子电池中的石墨经高温热解及酸浸处理后可以得到纯净的再生石墨,采用再生石墨增强水泥基复合材料的力学性能和电学性能。结果表明:再生石墨的引入可以增强材料的抗压性能和抗折性能,最大增幅分别达到了57.3%和84.4%。此外,再生石墨的加入有效降低了材料的电阻率,减少了极化时间,当再生石墨的掺加量为3%时,养护28 d后材料的电阻率仅为249 Ω·cm。该复合材料还具有典型的压敏特性。所制备的复合材料有望用于混凝土材料结构的实时动态监测。此外,对于废弃锂离子电池的全组分回收利用及功能水泥材料的研发具有重要意义。  相似文献   
7.
为改善相变储能过程中石蜡(PA)的熔化性能,向PA中添加少量膨胀石墨(EG)制备了4种配比的石蜡/膨胀石墨复合相变材料(PA-EG)。通过热物性分析筛选出合适配比的PA-EG,并对其和PA在水平管壳式相变储能单元中的熔化过程进行了实验研究。根据相变材料的温度场变化以及加权法计算得到的熔化分数变化,对比分析了添加EG前后PA的熔化性能,并探究了加热温度对相变材料熔化性能的影响。结果表明,PA-EG3的热导率比PA高了7倍,且两者的相变温度和潜热相差不大。PA-EG3熔化过程中的自然对流效应弱于PA,但是较高的热导率能够显著改善相变储能单元中下部的熔化,使得其整体熔化速度快于PA。当加热温度为80℃时,PA-EG3的熔化过程比PA缩短了78.16%。此外,降低加热温度会使PA和PA-EG3的完全熔化时间都显著增加,但相同条件下PA-EG3的增加幅度更小。  相似文献   
8.
采用无氰电镀工艺在TC4合金表面制备了Cu/石墨复合镀层,研究了镀层的组织结构和摩擦磨损行为。结果表明,采用无氰电镀方法能够在TC4合金表面制备出组织致密且与基体结合紧密的Cu/石墨复合镀层,但增加镀层中石墨的含量会降低镀层与基体合金的结合强度,并导致硬度小幅下降。摩擦磨损实验结果表明,Cu/石墨复合镀层具有优良的摩擦磨损防护性能,归因于石墨有效降低了镀层的摩擦系数和磨损率;对镀层磨损形貌、磨损产物和摩擦系数的综合分析结果表明,纯铜镀层的摩擦磨损机制主要为犁削磨损、黏着磨损和剥层磨损,Cu/石墨复合镀层的磨损机制为轻微的削层磨损和疲劳磨损。  相似文献   
9.
C-SiC composite powders were prepared by salt-assisted synthesis from Si powders, graphite, and a molten salt medium (NaCl and NaF) with the molar ratio of Si/C =?1/2 at 1300?°C for 3?h. After the C-SiC composite powders part and complete replacement of the graphite, the mechanical properties, oxidation resistance and slag-corrosion resistance of the Al2O3-C materials were studied by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), as well as with dedicated equipment. The results indicated that SiC whiskers, with lengths of 10–50?nm, formed on the surface of the flake graphite, and the activation energy of oxidation of the C-SiC composite powder increased by 45.72?kJ?mol?1 as compared to that of flake graphite. Furthermore, the decarburization area and slag erosion area of the Al2O3-C material decreased after 3?wt% of C-SiC composite powder was substituted for the flake graphite. Meanwhile, the cold modulus of rupture was maintained when 3?wt% of C-SiC composite powder was added. This improved both the oxidation and slag resistance of the Al2O3-C materials.  相似文献   
10.
Expanded graphite with nano SiC and amorphous SiCxOy coating was successfully prepared through pyrolysing silane coupling agent (SCA), where the grafting of SCA dominated the final products. The results show that mainly amorphous SiCxOy coating covers expanded graphite at 1000 °C, regardless of the SCA concentration. In comparison, nano SiC coating can be synthesized at 1200 °C depending on the good dispersion of SCA (with a SCA concentration of 50 vol%). The formed SiC coating contributes to much higher peak oxidation temperature (812.1 °C) than 678.0 °C of the pure expanded graphite. Meanwhile, the oxidation activation energies of expanded graphite are remarkably improved from 149.15 kJ/mol to 176.16 kJ/mol (based on Kissinger method), attributing to the derived nano SiC and SiCxOy coating.  相似文献   
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